mm miih miiih mm i « ; ; : n - * i TRANSACTIONS OF THE NEW ZEALAND INSTITUTE 1908 VOL. XLI (New Issue) EDITED AND PUBLISHED UNDER THE AUTHORITY OF THE BOARD OF GOVERNORS OF THE INSTITUTE Issued June, 1909 WELLIN'GTON, N.Z. JOHN MACKAY, GOVERNMENT PRINTING OFFICE KEGAN, PAUL, TRENCH, TRUBNER, AND CO., PATERNOSTER HOUSE CHARING CROSS ROAD, LONDON -ARYJ' CONTENTS. TEANSACTIONS. I. — Miscellaneous. PAGES. Art III. On a Method of carrying out the Decimal Currency. By H. Skey .. .. .. .. .. 16-22 VII. On the Harmonic Conic of Two Given Conies. By Evelyn G. Hogg, M.A. . . . . . . . . 34-37 VIII. On certain Couic-loci of Isogonal Conjugates. By Evelyn G. Hogg, M.A. . . . . . . . . . . 38-42 XXIII. Captain Dumont D'Urville's Visit to Tologa Bay in 1827. Translated from the French by S. Percy Smith, F.R.G.S. .. .. .. .. .. 130-139 XXIX. A Very Rare Maori Implement — Ahao. By Dr. A. K. Newman .. .. .. .. .. 216-218 XXX. On the Trisection of an Angle. By H. W. Segar, M.A... 218-221 XXXI. Insanity : Some Comparative Statistics. By H. W. Segar, M.A. .. .. .. .. .. 221-230 XXXII. Maori Forest Lore : Being some Account of Native Forest Lore and Woodcraft, as also of many Myths, Rites, Customs, and Superstitions connected with the Flora and Fauna of the Tuhoe or Ure-wera District : Part II. By Elsdon Best . . . . . . 231-286 XXXIII. A Contribution to our Knowledge of the Physiological Action of Tutin. By Frank Fitchett, M.D. (Edin.). . 286-366 XL. The Wellington Tide-gauge. By C. E. Adams, M.Sc, A.I.A. (Lond.), F.R.A.S. .. .. .. ..406-410 XLI. A Natural Classification of English Poetry. By Johannes C.Andersen .. .. .. .. .. 410-418 XLII. Development of Four - syllabled Metrical Unit in the Australian Modification of the English Ballad. By .Johannes C. Andersen .. .. .. .. 418-421 XLIII. New Zealand Bird-song. By Johannes C. Andersen .. 422-428 II. — Zoology. I. On the Nesting Habits of llhipidura flahellifera. By W. W. Smith . . . . . . . . . . 1-4 II. Notes and Descriptions of New Zealand Lepidoptera . By E. Meyrick, B.A., F.R.S., F.Z.S. .. .. .. 5-16 IV. A List of the Hendptera (excluding Sternorrhyncha) of the Maorian Subregion, with Notes on a Few of the Species. By G. W. Kirkaldy . . . . . . 22-29 V. Birds on Kapiti Island. By .James Drummond, F.L.S., F.Z.S. .. .. .. .. .. .. 30-32 3240;5 iv Contents. Art. X. Noces od Lepidoptera collected by H. Hamilton in various pages. Localities in the Queenstown District, Otago, between November, 1907, and March, 1908. By A. Hamilton 44-48 XIII. The Fresh-water Amphipoda of New Zealand. Bv Charles Chilton, M.A., D.Sc, F.L.S. .. . ." .. 53-59 XIV. Note on the Amohipodan Genera Bircenna, Kiiria, and iVaiidelia. By Charles Chilton, M.A., D.Sc, F.L.S. 59-63 XXII. Further Notes on New Zealand Starfishes. By H. Farquhar .. .. .. .. .. 126-129 XXVII. Notes on Coleoptern from the Chatham Islands. By Major T. Bromi, F.E.S. .. .. .. .. 145-151 XXVIII. Revision of the New Zealand Cossonida, with Descriptions of New Genera and Species. By Major T. Broun, F.E.S. .. .. .. .. .. .. 151-215 XXXIV. Notes on a New Zealand Actinian, Bunodes aureoradiata. By F. G. A. Stuckey, M.A. .. .. ..367-369 XXXV. On Two Anemones found in the Neighbourhood of Wel- lington, Leotealia thomsoni and Sugar tia alhocincta. By F. G. A. Stuckey, M.A. . . . . . . 370-374 XXXVI. A Review of the New Zealand Actiniaria known to Science, together with a Description of Twelve New Species. By F. G. A. Stuckey, M.A. . . . . 374-398 III. — Botany. XXIV. Description of a New Species of Epilobium. By D. Petrie, M. A., F.L.S. .. .. .. \. .. 140 XXV. Notice of the Discovery of a Species of Burmaimiacece, a Familv new to the New Zealand Flora. Bv T. F. Cheeseman, F.L.S., F.Z.S. .. .." .. 140-143 XXXVII. Some Hitherto-unrecorded Plant-habitats (IV). Bv L. Cockayne, Ph.D. .. .. .. " . . 399-403 XXXVUI. On a Collection of Plants from the Solanders. Bv L. Cockayne, Ph.D. .. .. .. ' .. 404-405 XXXIX. Note on Aerial Rhizomes in Cordyline australis. Bv L. Cockayne, Ph.D. .. .. .. .. " .. 405-406 XhY. On Dactylanthus Taylori. By H. Hill, B.A., F.G.S. .. 437-440 IV. — Geology and Chemistey. VI. Some Striated Stones from the St. Bernard Saddle, Upper Waimakariri Valley. By M. C. Gudex . . 33 IX. The Technical Analysis of Sliped Wool. Bv A. M. Wright, F.C.S. .. .. .. .! .. 42-43 XI. A Rapid and Accui-ate Method of esthiiating Iron in Iron-ores. Bv J. S. Maclaurin, D.Sc, F.C.S., and W. Donovan, M.Sc . . . . , . . . 49-51 XIL On a Hornblende-andesite from the Solander Islands. Bv R. Speight, M. A., B.Sc, F.G.S. .. .. .'. 52-53 XV. The Geology of the Quartz Veins of the Otago Goldfields. By A. M. Finlayson, M.Sc, A.O.S.M. .. .. 64-84 XVI. The Geology of the Reefton Gold-veins. By A. M. Fin- layson . . . . . . . . . . . . 85-98 Contents. Art. XVII. The Geology of Rarotonga and Aitutataki. Bv P. Mar- pages. shall, M.A., D.Sc, F.G.S. .. '. . .. 98-100 XVIII. Contact Rocks from West Nelson. By P. Marshall . . 101-102 XIX. Crater of Ngauruhoe. By P. Marshall . . . . 102-105 XX. Additions to the List of New Zealand Minerals. By P. Marshall .. .. .. .. .. 105-110 XXI. Geology of Signal Hill, Dunedin. By C. A. Cotton, M.Sc. 111-126 XXVI. Some New Zealand Fossil Cephalopods. By P. Marshall 143-145 XLIV. The Great Wairarapa : A Lost River. By H. Hill, B.A., F.G.S. 429-437 Plate. I. II. Ill, IV (Fig. 1). IV (Figs. 2, 3). V-VII. VIII-XI. XII. XIII, XIV. XIVa. XV, XVI. XVII. XVIII-XX. XXl-XXVIII. XXIX. XXX-XXXII. LIST OP PLATES. Striated Stones. — Gudex Quartz Veins of Otago Goldfields. — Finlayson Rarotonga and Aitutaki. — Marshall .. Contact Rocks of West Nelson. — Marshall Crater of Ngauruhoe. — Marshall Geology of Signal Hill. — Cotton New Zealand Starfish. — Farquhar D'Urville's Visit to Tologa Bay. — Smith New Zealand Fossil Cephalopods. — Marshall New Zealand Coxsonidce. — Broun A New Zealand Actinian. — Stuckey Two Anemones. — Stuckey A Review of New Zealand Actiniaria. — Stuckey Aerial Rhizomes in Cordyline australts. — Cockayne Dactyla7ithus Taylori. — 'H.iLij To illustrate Article VI XV XVII XVIII XIX XXI XXII XXIII XXVI XXVIII XXXIV XXXV XXXVI XXXIX XLV UJ I L I B R A R Y ^1 NEW ZEALAND INSTITUTE. ESTABLISHED UNDER AN ACT OF THE GENERAL ASSEMBLY OF NEW ZEALAND INTITULED "THE NEW ZEALAND INSTITUTE ACT, 1867"; RECONSTITUTED BY AN ACT OF THE GENERAL ASSEMBLY OF NEW ZEALAND UNDER "THE NEW ZEALAND INSTITUTE ACT, 1903." Board of Governors. EX OFFICIO. His Excellency the Governor. The Hon. the Colonial Secretary. NOMINATED BY THE GOVERNMENT UNDER CLAUSE 4. A. Hamilton; E. Tregear, E.E.G.S. ; John Young; J. W. Joynt, M.A. ELECTED BY AFFILIATED SOCIETIES UNDER CLAUSE 4. Wellington : Martin Chapman, K.C. ; Professor T. H. Easterfield, M.A., Ph.D. Auckland: D. Petrie, M.A., F.L.S. ; J. Stewart, C.E. Napier: H. Hill, B.A., F.G.S. Christchurch : E. Speight, M.A., B.Sc, F.G.S. ; C. C. Farr, D.Sc. Westland : T. H. Gill, M.A. Nelson : L. Cockayne, LL.D. Otago : Professor W. B. Benham, D.Sc, F.E.S. ; G. M. Thomson, F.L.S. , F.C.S., M.P. Manawatu : K. Wilson, M.A. OFFICERS FOR THE YEAR 1909. President: A. Hamilton. Hon. Treasurer: Martin Chapman, K.C. Editor of Transactions : G. M. Thomson, F.L.S., F.C.S. Secretary : B. C. Aston, F.C.S. AFFILIATED SOCIETIES. Wellington Philosophical Society Auckland Institute Philosophical Institute or Canterbury Otago Institute Westland Institute Hawke's Bay Philosophical Institute Southland Institute Nelson Institute Manawatu Philosophical Society DATE OP AFFILIATION. 10th June, 1868. 10th June, 1868. 22nd October, 1868. 18th October, 1869. 21st December, 1874. 31st March, 1875. 21st July, 1880. 20th December, 1883. 16th January, 1904. Vlll Neio ZealoMd Institute. HONOEAEY MEMBERS (elected since the inception of the institute). 1870. Agassiz, Professor Louis. Drury, Captain Byron, K.N. Finsch, Dr. Otto. Flower, Professor W.H., F.R.S. Hochstetter, Dr. Ferdinand von. Darwin, Charles. M.A., F.R.S. Gray, J. E., Ph.D., F.R.S. Grey, Sir George, K.C.B. Huxley, Thomas H., LL.D., F.R.S. Hooker, Joseph D., M.D., F.K.S., C.B Mueller, Ferdinand von, M.D., F.R.S., C.M.G. Owen, Professor Richard, F.R.S. Richards, Rear-Admiral G. H. 1871. Lindsay, W. Lauder, M.D., F.R.S. E. 1872. I Stokes, Vice- Admiral J. L. 1873. Bowen, Sir George Ferguson, G. C.M.G. Cambridge, the Rev. 0. Pickard, M.A., C.M.Z.S. 1874. Giinther, A., M.D., M.A., Ph.D., F.R.S. Lyell, Sir Coarles, Bart., D.C.L., F.R.S. McLachlan, Robert. F.L.S. Newton, Alfred, F.R.S. Filhol, Dr. H. Rolleston, Professor G., M.D., F.R.S. Berggren, Dr. S. Clarke, Rev. W. B., M.A., F.R.S. Baird, Professor Spencer F. Sharp, D., M.D. Garrod, Professor A. H., F.R.S. Miiller, Professor Max, F.R.S. I Thomson, Professor Wyville, F.R.S. 1875. Sclater, Philip L., M.A., Ph.D., F.R.S. 1876. Etheridge, Professor R., F.R.S. 1877. j Weld, Frederick A., C.M.G. 1878. Tenison- Woods, Rev. J. E., F.L.S. 1880. The Most Noble the Marquis of Normanby, G.C.M.G. 1883. Carpenter, Dr. W. B., C.B., F.R.S. Ellery, Robert L. J., F.R.S. Gray, Professor Asa. Sharp, Richard Bowdler, M.A., F.L.S. Beneden, Professor J. P. van. Ettingshausen, Baron von. I Thomson, Sir William, F.R.S. 1885. Wallace, R. A., F.L.S. 1888. McCov, Professor F., D.Sc, C.M.G., F.R.S. Honorary Members. ix 1890. Liversidge, Professor A., M.A., F.R.S. Nordstedt, Professor Otto, Ph.D. Riley, Professor C. V. 1891. Davis, J. W., F.G.S., P.L.S. | Goodale, Professor G. L , :\r.D., LL.D. 1894. Codrington, Rev. R. H., D.D. I Dyer, Professor W. Thiselton. M.A., I C.M.G., F.R.S. 1895. Mitten, William, F.R.S. 1896. Langley, S. P. 1 Lydekker, Richard, B. A., F.R.S. 1900. XC^^^3 Masses, George, F.L.S., F.R;i^<^0 ^/\^^\ 1901. luji LIBRARY jac Eve, H. W., M.A. I Howes, G. B., LL.D.. F.R.B.- Goebel, Dr. Carl. I 1902. Sars, Professor G. 0. 1903. Klotz, Professor Otto J. 1904. David, Professor T. Edgeworth, F.R.S. | Rutherford, Professor E., D.Sc, F.R.S. 1906. Brady, G. S., F.R.S. Agardh, Dr. J. G. Lubbock, Sir John, Bart., P.O., F.R.S Beddard, F. E., F.R.S. Milne, J., F.R.S. Dandy, Dr., F.R.S. Diels, L., Ph.D. 1907, Mevrick, E., B.A., F.R.S. Stebbing, Rev. T. R. R,, F.R.S. 1908. Darwin, Sir George, F.R.S. PRESIDENTS. 1903-4. Hutton, Captain Frederick Wollaston, F.R.S. 1905-6. Hector, Sir James, M.D., K.G.M.G., F.R.S. 1907-8. Thomson, George Malcolm, F.L.S., F.G.S. 1909. Hamilton, Augustus. NEW ZEALAND INSTITUTE ACT. The following Act reconstituting ihe Institute was passed by Par- liament : — 1903, No. 48. An Act to reconstitute the New Zealand Institute. [18th November, 1903. "Whereas it is desirable to reconstitute the New Zealand Institute with a view lo connecting it more closely with the affiliated institutions : Be it therefore enacted by the General Assembly of New Zealand in Parliament assembled, and by the authority of the same, as follows : — 1. The Short Title of this Act is "The New Zealand Institute Act, 1903." 2. "The New Zealand Institute Act, 1867," is hereby repealed. 3. (1.) The body hitherto known as the New Zealand Institute (here- inafter referred to as "the Institute") shall consist of the Auckland Institute, the Wellington Philosophical Society, the Philosophical Insti- tute of Canterbury, the Otago Institute, the Hawke's Bay Philosophical Institute, the Nelson Institute, the Westland Institute, the Southland Institute, and such others as may hereafter be incorporated in accordance with regulations to be made by the Board of Governors as hereinafter mentioned. (2.) Members of the above - named incorporated societies shall be ijjso facto members of the Institute. 4. The control and management of the Institute shall be in the hands of a Board of Governors, constituted as follows : — The Governor ; The Colonial Secretary ; Four members to be appointed by the Governor in Council during the month of December, one thousand nine hundred and three, and two members to be similarly appointed during the month of December in every succeeding year ; Two members to be appointed by each of the incorporated societies at Auckland, Wellington, Christchurch, and Dunedin during the month of December in each alternate year ; One member to be appointed by each of the otlier incorporated societies during the month of December in each alternate year. 5. (1.) Of the members appointed by the Governor in Council two shall retire annually on the appointment of their successors ; the first two members to retire shall be decided by lot, and thereafter the two mem- bers longest in office without reappointment shall retire. (2.) Subject to the provisions of the last preceding subsection, the appointed members of the Board shall hold office until the appointment of their successors. 6. The Board of Governors as above constituted shall be a body cor- porate, by the name of the " New Zealand Institute," and by that name they shall have perpetual succession and a common seal, and may sue and be sued, and shall have power and authority to take, purchase, and bold lands for the purposes hereinafter mentioned. Neio Zealand Institute. xi 7. (1.) The Board of Governors shall have power to appoint a fit person, to be known as the " President," to superintend and carry out all necessary work in connection with the affairs of the Institute, and to pro- vide him with such further assistance, as may be required. (2.) It shall also appoint the President or some other fit person to be editor of the Transactions of the Institute, and may appoint a com- mittee to assist him in the work of editing the same. (3.) It shall have power to make regulations under which societies may become incorporated to the Institute, and to declare that any incorporated society shall cease to be incorporated if such regulations are not complied with, and such regulations on being published in the Gazette shall have the force of law. (4.) The Board may receive any grants, bequests, or gifts of books or specimens of any kind whatsoever for the use of the Institute, and dispose of them as it thinks fit. (5.) The Board shall have control of the property hereinafter vested in it, and of any additions hereafter made thereto, and shall make regu- lations for the management of the same, for the encouragement of research by the members of the Institute, and in all matters, specified or unspecified, shall have power to act for and on behalf of the Institute. 8. Any casual vacancy on the Board of Governors, howsoever caused, shall be filled within three months by the society or authority that appointed the member whose place has become vacant, and if not filled within that time the vacancy shall be filled by the Board of Governors. 9. (1.) The first annual meeting of the Board of Governors herein- before constituted shall be held at Wellington on some day in the month of January, one thousand nine hundred and four, to be fixed by the Governor, and annual meetings of the Board shall be regularly held thereafter during the month of January in each year, the date and place of such annual meeting to be fixed at the previous annual meeting. (2.) The Board of Governors may meet during the year at such other times and places as it deeuiS necessary. (3.) At each annual meeting the President shall present to the meeting a report of the work of the Institute for the year preceding, and a balance- sheet, duly audited, of all sums received and paid on behalf of the Institute. 10. The Board of Governors may from time to time, as it sees fit, make arrangements for the holding of general meetings of members of the Institute, at times and places to be arranged, for the reading of scientific papers, the delivery of lectures, and for the general promotion of science in the colony by any means that may appear desirable. 11. The Colonial Treasurer shall, without further appropriation than this Act, pay to the Board of Governors the annual sum of five hundred pounds, to be applied in or towards payment of the general current expenses of the Institute. 12. (1.) On the appointment of the first Board of Governors under this Act the Board of Governors constituted under the Act hereby repealed shall cease to exist, and the property then vested in, or belong- ing to, or under the control of that Board shall be vested in His Majesty for the use and benefit of the public. - (2.) On the recommendation of the President of the Institute the Governor may at any time hereinafter, by Order in Council, declare that any part of such property specified in the Order shall be vested in the Board constituted under this Act. X Ne^o Zealand Institute. 13. All regulations, together with a copy of the Transactions of the Institute, shall be laid upon the table of both Houses of Parliament within twenty clays after the meeting thereof. REGULATIONS. The following are the new regulations of the New Zealand Institute under the Act of 1903 : — The word "Institute" used in the following regulations means the New Zealand Institute as constituted by " The New Zealand Institute Act, 1903." Incokporation of Societies. 1. No society shall be incorporated with the Institute under the provisions of " The New Zealand Institute Act, 1903," unless such society shall consist of not less than twenty-five members, subscribing in the aggregate a sum of not less than £25 sterling annually for the pro- motion of art, science, or such other branch of knowledge for which it is associated, to be from time to time certified to the satisfaction of the Board of Governors of the Institute by the President for the time being of the society. 2. Any society incorporated as aforesaid shall cease to be incorporated with the Institute in case the number of the members of the said society shall at any time become less than twenty-five, or the amount of money annually subscribed by such members shall at any time be less than £25. 3. The by-laws of every society to be incorporated as aforesaid shall provide for the expenditure of not less than one -third of the annual revenue in or towards the formation or support of some local public museum or library, or otherwise shall provide for the contribution of not less than one-sixth of its said revenue towards the extension and main- tenance of the New Zealand Institute. 4. Any society incorporated as aforesaid which shall in any one year fail to expend the proportion of revenue specified in Regulation No. 3 aforesaid in manner provided shall from henceforth cease to be incor- porated with the Institute. 5. All papers read before any society for the time being incorporated with the Institute shall be deemed to be communications to the Insti- tute, and then may be pubhshed as Proceedings or Transactions of the Institute, subject to the following regulations of the Board of the Institute regarding publications : — Regulations kegabding Publications. [CI.) The publications of the Institute shall consist of — (1.) A current abstract of the proceedings of the societies for the time being incorporated with the Institute, to be intituled " Proceedings of the New Zealand Institute " ; (2.) And of transactions comprising papers read before the incorporated societies (subject, however, to selection as here- inafter mentioned), and of such other matter as the Board of Governors shall from time to time determine to publish, to be intituled " Transactions of the New Zealand Institute." {b.) The Board of Governors shall determine what papers are to be published. (c.) Papers not recommended for publication may be returned to their authors if so desired. Regulations. xiii {d.) All papers sent in for publication must be legibly written, type- written, or printed. (e.) A proportional contribution may be required from each society towards the cost of publishing Proceedings and Transactions of the Institute. (/.) Each incorporated society will be entitled to receive a propor- tional number of copies of the Transactions and Proceedings of the New Zealand Institute, to be from time to time fixed by the Board of Governors. General Eegulations. 6. All property accumulated by or with funds derived from incor- porated societies, and placed in charge of the Institute, shall be vested in the Institute, and be used and applied at the discretion of the Board of Governors for public advantage', in like manner with any other of the property of the Institute. 7. Subject to " The New Zealand Institute Act, 1903," and to the foregoing rules, all societies incorporated with the Institute shall be entitled to retain or alter their own form of constitution and the by-laws for their own management, and shall conduct their own affairs. 8. Upon application signed by the President and countersigned by the Secretary of any society, accompanied by the certificate required under Eegulation No. 1, a certificate of incorporation will be granted under the seal of the Institute, and will remain in force as long as the fore- goiirg regulations of the Institute are complied with by the society. 9. In voting on any subject the President is to have a deliberate as well as a casting vote. Management of the Property of the Institute. 10. All donations by societies, public Departments, or private indi- viduals to the Institute shall be acknowledged by a printed form of receipt, and shall be entered in the books of the Institute provided for that purpose, and shall then be dealt with as the Board of Governors may direct. Honorary Members. 11. The Board of Governors shall have power to elect honorary members (being persons not residing in the Colony of New Zealand), pro- vided that the total number of honorary members shall not exceed thirty. 12. In case of a vacancy in the list of honorary members, each incor- porated society, after intimation from the Secretary of the Institute, may nominate for election as honorary member one person. 13. The names, descriptions, and addresses of persons so nominated, together with the grounds on which their election as honorary members is recommended, shall be forthwith forwarded to the President of the New Zealand Institute, and shall by him be submitted to the Governors at the next succeeding meeting. 14. The President may at any time call a meeting of the Board, and shall do so on the requisition in writing of four Governors. 15. Twenty-one days' notice of every meeting of the Board shall be given by posting the same to each Governor at an address furnished by him to the Secretary. 16. In case of a vacancy in the office of President, a meeting of the Board shall be called by the Secretary within twenty-one days to elect a new President. xiv Neiv Zealand histitute. 17. The Governors for the time being resident or present in Wellington shall be a Standing Committee for the purpose of transacting urgent business and assisting the officers. 18. The Standing Committee may appoint persons to perform the duties of any other office which may become vacant. Any such appoint- ment shall hold good until the next meeting of the Board, when the vacancy shall be filled. 19. The foregoing regulations may be altered or amended at any annual meeting, provided that notice be given in writing to the Secretary of the Institute not later than the 30th November. TRANSACTIONS OF THE NEW ZEALAND INSTITUTE, 1908. Akt. I. — On the Nestimj Habits of Rhipidura flabellifera. I By W. W. Smith. [Read before the Manawatu Philosophical Society, IQth March, 1908.] The native fantails or fly-catchers are, by their abundance and airy and graceful evolutions on the wing when in pursuit of their tiny prey, perhaps the best-known birds at the present time in the New Zealand avifauna. By reason of there being few ornithological observers in the early days of settlement, and the rapid extinction of species proceeding meanwhile, the latter have nearly all vanished without science knowing anything — or, at least, very little — of their nesting habits, or of the respective periods of time occupied during their incubation. Although the late Sir Walter BuUer has given a good general history, with very perfect delineations of each species, only in three cases has he referred to their approximate time - periods of incubation. His great industry during his early life in compiling general and accurate histories of all species coming under his observation occupied his full time, and frequently prevented him from observing and noting their several and perfect habits and full periods of hatching. It may there- fore be of interest to members of our Society to have complete and accurate notes on the nesting habits of the fantail, from the hour of lacing the first twig on to -the forked site of the nest to that of the four young fledglings reared therein leaving it for the 'first time. For many years two pairs of these charming little birds have built their nests in Mr. W. Park's garden at " The Wattles," Palmerston North. On hearing of this a year ago, and being much interested, I requested Mr. Douglas Park to observe and make absolutely accurate notes of the brood or broods of young fantails. With kindly and commendable patience and perseverance Mr. Park, jun., daily closely observed and accurately noted all phases of life of the parent birds when engaged nesting. On the 9th August, 1907, a pair began to construct a nest in the fork of a climbing rose trained on the outside of a summer-house in the shade of native trees. After working earnestly and many hours per day for four days the birds apparently became displeased with their work and discon- tinued operations. Inside the roof of the summer-house some stems of clematis have grown down through the air-passages and formed a small com- pact network of growth. On one of these stems the fantails chose a site for 1— Trans. 2 Transactions. a new nest, and immediately began to demolish the unfinished structure, and use the same materials with which to rebuild it. " The work of con- structing the second nest," writes Mr. Park, jun., " was started on the 14th August, and was finished on the 31st. They laid four eggs — the first on the day they completed the nest, and one on each morning following until the 4tli. At 10 a.m. they commenced sitting — each parent taking turns on the nest until the young birds were hatched on the 21st. The young ones were full-fledged and flew away at about 10 a.m. on the 30th September." The time-period of incubation of the New Zealand fly-catcher therefore occupies a full day less than that of any European species of the genus as recorded in the works of British ornithologists. Whilst engaged dismantling the partially finished nest, and utihsing the materials with which to build the new one in the dome of the summer- house, the birds would alight occasionally on the side of the nest, and, fixing their feet thereon, would use their full strength in dra%ving asunder with their beaks the tightly and closely woven materials. They displayed great activity at their work, meanwhile uttering notes of apparent in- struction and approval to each other. The male performed most of the work of carrying the materials to the new site, while the female did most of the work in building the nest. When the young birds were hatcJied the parent birds continued to hunt vigorously on the wing for tiny insects with which to feed them. AVhen not hunting on the Aving for their own sus- tenance the parent birds — especially the male — frequently sat close to its mate hatching, and occasionally on the rim of the nest. The habit is prac- ticed by many species of birds, but more especially by those of the group to which the fly-catchers belong. Mr. Park states that the weather, being very wet and boisterous while the nest was in course of building, retarded considerably the progress of their work at it. On the 16th January last we observed a pair of fantails hunting assidu- ously and passing frequently into a " lacebark " tree {Hoheria populnea) growing on the Victoria Esplanade, Palmerston North. On looking up through the branches I located the nest, which contained three young birds. They remained in the nest until about noon the following day, when they left it and fluttered along towards the extremity of the bough bearing the nest. The weather being hot and calm, they remained sitting near each other for nearly two days, and were well fed meantime by their active parents. On the 21st they separated, and were fed at times for several days after leaving the " lacebark " tree in which they were reared. It was indeed interesting to observe these young fantails flitting gracefully from bough to bough or from tree to tree, as if training and developing their wings, by which they were soon to become self - dependent. These birds are now expert fly-catchers, and belong to a group of about twenty individuals regularly inhabiting the Esplanade and its environs. Nearly all trees of Hoheria populnea and its varieties ^ZancfoZoto and angustifolia, with Plagi- anthus hetiiUnns, have been extremely floriferous on the Esplanade during the late-early and midsummer months. The great masses of scented white flowers they produce are a great attraction to all classes of insect. On calm days, when insects were plentiful at the flowers, the fantails were generally close to them on the -wing, having a royal time subsisting on the numerous small insects, chiefly Diptera, passing to and from the flowers. After feeding for several minutes on the wing on the minute flies frequent- ing the blossoms, the birds would, dart through the outer branches, and, resting for a few minutes within them in the shade, would again dart swiftly Smith. — On tJie Ncating Habits of Ehipidura flabellifera. 3. out in pursuit of their prey as it hove ui sight. These graceful little birds possess remarkably quick and clear vision, while their minute and delicate beaks may occasionally be distinctly heard snapping at their prey as they flit near the observer. When at Tirotiro-moana Valley, in Taranaki, on the 7th August, 1905, I observed a pair of fantails constructing a nest on a Hmb of tutu-shrub partly overhanging the road formed obliquely along the steep east side of the valley. They were using mosses and lichens chiefly, and, as with the pair studied by Mr. Douglas Park, the male was carrying the materials, while the female wove them expertly and neatly into the nest. For about two minutes during the half-hour I watched them the male assisted in placing and fixing the materials it brought into the structure. They were working with great vivacity and vigour, meanwhile twittering freely to each other. The female seemed to work fretfully, but with perfect precision, and was a little fastidious in the selection of the materials brought by her mate wherewdth to build the nest. They were working with great activity when I reluctantly left them. When engaged preparing these notes I received an interesting letter from Mr. D. Sinclair, C.E., of Terrace End, Palmerston North, narrating a remarkable experience mth a fantail's nest, which I have pleasure in reproducing here. " While I was engineer for the Pohangina County Council," writes Mr. Sinclair, " I was using a slasher cutting a line through the bush. In doing so I cut a small branch of a rather bushy tawhara, which often grows on the side of a tree-fern. The branch fell from the slasher upside down, when I noticed a fantail's nest, and, to my surprise, found that the bird was on the nest, and, although it was upside down, the bird was clinging so ten- aciously to the nest that it prevented the Httle eggs (four in number) from falling out. The little bird sat on the nest with its eyes closed, and seemed oblivious to the rough ordeal it was being subjected to. I lifted it partly off the nest to count the number of eggs, when it hustled itself down again in the nest, saying in efl'ect, if not in words, without sound or motion, ' Do what you will with me, I am going to stick to my nest.' Maternity seemed for the moment to outweigh all sense of danger in the little fantail. I carried it a little distance in the bush from where the line was being cut. and inserted the branch in an upright position in the trunk of another fern- tree, with the hope that the fearless little mother would be rewarded in due time with four little fantails." To Mr. Park, jun., is due the honour of first observing and ascertaining precisely the respective time-periods of nest-bmlding, egg-laying, and hatch- ing of the native fantail fly-catcher, which constitutes a valuable addition to our knowledge of the habits of the species. Though these birds are still fairly numerous, there is some probability of them becoming rarer as the native bush disappears. In parts of the South Island they adapt them- selves to wholly altered conditions to those of the native bush during the winter months. On the approach of cold weather in the bush remaining in some of the valleys of the fore hills of other ranges in Canterbury the fantails migrate across the plains and live in the plantations and shubberies around the settlers' homes, until the nesting instinct returns with the warmth of spring, when they again repair to the bush to nest for the season. The nest of the native fantail ranks amongst the neatest and best-finished of its class, and is an excellent model of bird-architecture. A closer exam- ination of the methods of lacing together the soft mosses, lichens, tiny leaves. 4 Transactions. and pappus with threadlike tendrils and roots, all collected in the bush, into a beautiful and compact structure, imparting great warmth, further en- hances admiration of its instinctive work. The graceful habits and delight- ful twitterings when flitting through and on the outskirts of our perennially green forests in pursuit of minute prey are likewise some of the more pleasing scenes of native bird-life to be seen and enjoyed in this beautiful country. No words or language could adequately express the feelings of regret of the true naturalist and nature-lover to know that already, within the period of fifty years of settlement in New Zealand, some of the most remarkable species of birds man has seen or science known have vanished for ever from our green forests, grassy plains, and reedy swamps, which almost everywhere existed in their full native beauty when European settle- ment began. It may be of interest to note some of the sites on which nests of the fantail have been observed in the North Island : — 1. On the matipo-tree {Myrsine Urvillei) in Mr. Park's garden, Palmerstou North ; September, 1905. 2. On a mahoe {Mclicytus ramifiorus) at Hawera ; October, 1905. 3. On a tutu-shrub {Coriaria ruscifolia) at Tirotiro-moana, Taranaki ; 7th August, 1905. 4. On a Magnolia qrandiffora in Mr. Park's garden, Palmerston North ; October, 1906. 5. On a young totara {Podocarpus totara) in Mr. Barton's garden, Fare- ham, Featherston ; October, 1907. 6. On clematis inside roof of summer-house in Mr. Park's garden, Pal- merston North : August and September, 1907. 7. On Hoheria popuhica, Victoria Esplanade (an area of native bush) ; January, 1908. 8. On tawhara {Freycinctia Banlsii)' on trunk of fern-tree, Kimbolton bush ; no month or year given. (Mr. D. Sinclair.) 9. On tutu (Coriaria rvsci folia), Pakekura Park, New Plymouth ; October and November, 1906. (W. Pycroft.) Having in view the rapid and inevitable passing of the native birds, it invariably seems to me to be the bounden duty of observers of the pre- sent time to place on permanent record all facts respecting them, for the information and delight of generations who are to follow us. To me there is no ornithological subject more urgent. The remark would also apply to many remarkable species belonging to other groups of the New Zea- land fauna, and to many rare species of plants, now threatened with •extinction. Meyrick. — Notes and Descriptions of Netv Zealand Lepidoptera. 5 |uJ I L I B R A R Y Art. II. — Notes and Descriptions of New Zealand Lepidoptera. . s>/M By E. Meyrick, B.A., F.R.S., F.Z.S. # V Communicated by G. V. Hudson, F.E.S. [Read before the Wellington Philosophical Society, Qth May, 1908.] 1 AM again indebted for the material of these notes to the energetic assistance of my valued correspondents, Mr. G. V. Hudson, of Wellington, and Mr. A. Philpott, of Invercargill. Caradrinid^. Leucania phaula, Meyr. L. neurce, Philp. (Trans. N.Z. Inst., 1904, 330), is a synonym of this species. Mr. Philpott kindly sent me two examples of his species, himself suggesting that it might be identical with my phaula, and this is undoubtedly the case. Plusiad^. Plusia transfixa, Walk. Mr. Hudson sent me several examples of this species from the Thames district. It is common and widely distributed in eastern Austraha, where it is undoubtedly native ; it has not been hitherto recorded from New Zealand, and may perhaps have only recently succeeded in introducing itself. The species of this genus are strong and bold fliers, and can cross wide seas. Hydriomenid^. Eucymatoge anguligera, Butl. S t . 32-37 mm. Head and thorax whitish-ochreous, partially sprinkled with brown-reddish ; thorax with an irregular transverse anterior reddish- fuscous or dark-fuscous hne. Abdomen whitish-ochreous sprinkled with brown-reddish, with a bar of blackish suffusion on apex of second segment, and sometimes a double dorsal series of blackish dots. Forewings triangular, costa posteriorly moderately arched, apex obtuse, termen bowed, obUque, strongly waved ; pale brownish-ochreous, with numerous waved ferruginous- brown striae, tending to be somewhat marked with black on veins and costa ; median band somewhat paler through obsolescence of strioe, limited by groups of striae more distinctly marked with black, anterior curved, posterior rounded-prominent beneath costa and in middle, latter prominence suffused with blackish ; an oblique subapical patch of darker brown suffusion, its upper edge defined and running from above median prominence to apex : cilia pale ochreous mixed with brown-reddish, basal half sprinkled with dark fuscous. Hindwings with termen rounded, irregularly waved-dentate ; colour and stria? as in forewings, but prominences of median band nearly obsolete ; a blackish discal dot ; ciUa as in forewings. 6 Transactions. Invercargill, common on flowers of Senecio in March (Philpott) ; two specimens. Much. Hke gohiata, from which it may be certainly distinguished by the much more strongly waved termen of both wings ; gohiata is also rather smaller, whiter-irrorated, with straighter strise, lower half of anterior margin of median band and obUque streak from apex forming distinct black hues. I formerly quoted Butler's name erroneously as a synonym of gobiala. Xanthorhoe adonis, Huds. Having received two fine specimens from Mr. Philpott, I am satisfied it is a good. species, and readily distinguished from beata by the colour of the hindwings. Notoreas fulva, Huds. {Lythria jniva, Huds., Trans. N.Z. Inst., 1904, 357.) According to two 9 specimens communicated by Mr. Hudson, this species is a true Notoreas. Selidosemid^. Selidosema leucelaea, n. sp. (^ 30-32 mm., $ 27-30 mm. Head white or ochreo us- whitish, somewhat mixed with grey and dark fuscous, anterior half of crown in $ suffused with ochreous. Antennal pectinations of J : a, 9 ; h, 6. Thorax whitish, anteriorly irregularly marked with blackish, and in J partially suffused with brownish-ochreous. Abdomen whitish-ochreous tinged with grey. Forewings triangular, costa somewhat bent beyond middle, termen rounded, somewhat obhque ; white, more or less strewn with black or in J brownish specks and strigulse ; in 3 the whole wing is more or less suffused with grey or ohve-brown, except a straight white fascia (usually interrupted in middle) before subterminal line, and more or less of dorsal area towards middle, and there is usually a broad streak of brown suffusion beneath costa and another along termen, in ? there is no brown colouring, but some- times some grey suffusion ; basal area more or less marked with blackish ; first and second hnes more or less indicated bv white marks, enclosed between thick blackish more or less interrupted waved Unes, first obtusely angulated above middle, second nearly straight, sinuate near dorsum ; median cloudy, blackish, sinuate, interrupted ; discal spot transverse-linear, black, beyond median hne ; subterminal line slender, waved, white, partially edged an- teriorly with blackish suffusion, and followed by grey or brown suffusion : ciha grey, barred in 3 with brownish, in 5 with white. Hindwings pale whitish-ochreous, sometimes tinged with grey, sometimes darker posteriorly ; a grey discal dot ; two or three waved grey hnes sometimes more or less developed posteriorly ; a terminal series of blackish-grey crescentic marks : cilia whitish-ochreous, obscurely barred with greyish. Christchurch, Otira Gorge, Dunedin, Invercargill ; from January to March, and in July ; seven specimens. I have possessed examples of this species for a long time, but did not feel sure of their status, the species being a very variable one, and alUed to other variable species ; having now, however, received four very fine specimens from Mr. Philpott, I am satis- fied that it is a good species. Mr. Philpott writes that it is usually con- fused in collections with productata ; it is, however, nearer melinata, from which it differs by the much longer antennal pectinations, less rounded termen of forewings, distinct and unusually straight white posterior fascia ,. Meyeick. — Notes and Descriptions of New Zealand Lepidoptera. 7 liindwings of c? not tinged with fuscous towards base, and other details. S. productala is also very variable, but easily distinguished by different form of median band, of which the posterior margin is obtusely angulated rather above middle ; in fact, all the allied species could be distinguished by the form of the posterior margin of median band, which is different in «ach. Selidosema lupinata, Feld. *S. humillima, Huds., is a synonym of this species, according to specimens sent me by Mr. Philpott, by request of Mr. Hudson. Pyraustid^.. Scoparia gyrotoma, n. sp. 3 . 20 mm. Head pale ochreous, sides mixed with whitish. Palpi 2|, grey sprinkled with whitish, white towards base beneath. Antennae blackish, ciliations \. Thorax pale brassy-ochreous sprinkled with grey, margins suffused with whitish. (Abdomen broken.) Forewings elongate, narrow, gradually dilated, costa sinuate in middle, apex obtuse, termen shghtly rounded, somewhat obhque ; Hght brassy - yellowish - fuscous, suffusedly irrorated with white and sprinkled with dark fuscous ; an obUque fascia of blackish suffusion near base ; Unes thick, suffused, whitish, first rather indented on fold, followed by a fascia of blackish irroration, second shghtly angulated above middle, preceded by a fascia of blackish irroration ; orbi- cular and claviform coalescing to form an 8-shaped blotch of blackish suf- fusion with two whitish centres, coniiuent with blackish fascia of first hne ; a smaller 8-shaped discal spot outhned wdth blackish and filled with whitish, its lower extremity confluent with margin of second line ; terminal area irrorated with blackish, subterminal hne represented by broad cloudy whitish suffusion not reaching tornus : ciha whitish, with a grey median shade, basal half barred with darker grey. Hind wings 1^, grey- whitish, costa and termen narrowly suffused with hght grey ; ciha white. Lake Tekapo ; one specimen (Hudson). Alhed to S. asaleuta, but very distinct. Scoparia cyptastis, n. sp. 3 2 . 17-20 mm. Head grey, more or less mixed or suffused with white. Palpi 3, dark-grey, sprinkled with white above, wholly white towards base beneath. Antennae dark fuscous, cihations in J ^. Thorax dark purplish- grey sprinkled with whitish. Abdomen whitish-ochreous, more or less sprinkled with grey. Forewings elongate, narrow at base, obhque ; fuscous, variably mixed or suffused with whitish, veins tending to be more or less streaked with dark fuscous or blackish ; a black streak on fold from base to first line, interrupted in middle by a white spot ; hnes thick, white, first curved, little obhque, more or less edged with dark fuscous posteriorly, second slightly curved, indented beneath costa and sinuate above dorsum ; orbicular and claviform small, rather elongate, black, orbicular sometimes touching edge of first line ; discal X-shaped, black ; subterminal hne cloudy, whitish, entire, irregular, not touching second hne ; a terminal series of black marks on veins : ciha whitish, with rather dark fuscous basal and paler median shades. Hindwings IJ, without long hairs in cell ; pale whitish- fuscous, with a faint yellowish tinge, termen suffused with fuscous, more strongly in ? : cilia whitish, with two hght-fuscous shades, basal darker in 2 . 8 Transactions Invercargill, common in November (Philpott) ; three tpecimens. Be- longs to the deoclorah's group ; not very like any New Zealand species, but probably related to the Tasmanian plagiotis and its allies. Scoparia luminatrix, n. sp. S 9 . 19-22 mm. Head rather dark fuscous, sprinkled with whitish and mixed on crown with, yellow-ochreous. Palpi 3, dark fuscous sprinkled with whitish, towards base white beneath. Antennae dark fuscous, ciliations in c? I- Thorax fuscous mixed with dark fuscous and whitish. Abdomen fuscous, segmental margins ochreous-whitish. Forewings very elongate- triangular, costa slightly arched, somewhat bent posteriorly, apex obtuse, termen rather oblicjuely rounded ; deep ochreous-brown, suft'usedly streaked mth blackish on veins, especially tending to form a median longitudinal black streak interrupted by lines ; first and second lines white, well marked, first curA^ed, waved, Uttle oblique, edged posteriorly with black suffusion. on upper half sometimes broadly, second slightly curved, indented towards costa, and sinuate above dorsum ; median band much mixed with white, especially towards second line below middle, where it sometimes forms a conspicuous patch of white suffusion ; orbicular and claviform small, round, partially outlined with black, and filled with whitish, sometimes absorbed in black suffusion of first line ; discal indistinct, 8-shaped, white, partiallv edged with black ; subterminal line cloudy, whitish, remote from second throughout, indistinctly interrupted above middle : cilia whitish, with two grey shades interrupted by white bars. Hindwings IJ, with long hairs in cell ; whitish-fuscous tinged with brassy-yellowish ; discal spot, post- median line, and a terminal fascia indistinctly fuscous ; cilia fuscous-whitisli. with two fuscous shades. Invercargill, in October and November ; five specimens (Philpott). Eather variable in the development of the black and white scales. A distinct species, somewhat intermediate between legnota and ejncremna. ^ , . ^ Crambid^. Crambus sanstes, n. sp. 3 . 17-18 mm.. Head and thorax ferruginous-brown, face prominent, flattened-conical ; edge of collar and a spot on shoulders whitish. Palpi 3J, brown mixed with dark fuscous, whitish towards base beneath. Antennse dark fuscous, pubescent-ciliated (|). Abdomen dark grey. Forewings elon- gate, gradually dilated, costa slightly arched, apex obtuse, termen little rounded, rather oblique ; bright ferruginous-brown ; a slender median longitudinal rather irregular ochreous-whitish streak from base to termen, terminal fifth attenuated and tending to be obsolescent : cilia slaty-grey. Hindwings dark-grey ; cilia pale-grey, basal third slaty-grey. Under- surface dark-grey, hindwings sometimes with very slender indistinct median streak of whitish suffusion ; costal edge of hindwings whitish-yellowish ; all ciha whitish-grey. Invercargill, in January (Philpott) ; two specimens. Very close to heteranihes from Mount Cook, but that species is darker, median streak of forewings whiter, broader, more regular, forewings on under-surface with dorsum suffused with white, hindwings on under-surface with costa suffused with white towards base, and well-marked white median streak, cilia white towards base. Possibly more extensive material may show this to be a local form of heteranthes, but at present it seems better to treat them as distinct. Meyeick. — Notes and Descriptions of Neiv Zealand Lepidoptera. 9 Crambus aulistes, n. sp. J . 16 mm. Head, palpi, and thorax ferruginous-brown, face rounded- prominent ; palpi 4, whitish towards base beneath. Antenna dark fuscous, pubescent-ciUated (f). Abdomen rather dark fuscous. Forewings elongate, broader than in saristes, costa gently arched, apex obtuse, termen straight, rather oblique, rounded beneath ; ferruginous-brown ; a moderate regular white median longitudinal streak from base to termen, somewhat edged with fuscous suffusion towards middle : ciha pale grey, with darker basal shade, on costa whitish except near apex, with a white bar on terminal extremity of median streak. Hindwings dark fuscous ; cilia whitish, basal third fuscous. Under- surface dark grey, forewings much suffused with yel- lowish towards costa and termen, on dorsum broadly whitish-yellowish, hindwings with costa rathex broadly pale ochreous-yellowish, with veins suifusedly streaked with pale yellowish, especially on a median streak, all cilia whitish. Invercargill (Hudson) ; one specimen. Distinguished from the preceding by the broader forewings, rather longer palpi and antennal ciliations, white costal cilia, extensive yellowish suffusion of under-surface, and other details. Crambus melitastes, n. sp. S 9 . 17-20 mm. Head, palpi, and thorax ochreous-brown, in 9 with a broad dorsal white stripe extending through crown and thorax, face some- what rounded-prominent ; palpi 4, whitish beneath and more or less above, especially in 9 . Antennte dark fuscous, in J simply ciliated (|). Abdomen rather dark fuscous, more or less whitish on segmental margins posteriorly. Forewings elongate, gradually dilated, costa hardly arched, apex obtuse, termen straight, rather oblique, rounded beneath ; ochreous-brown ; a moderate white median longitudinal streak from base to termen, slightly broadest in middle, in 3 more or less edged beneath with dark-fuscous suffusion, in 9 broadly edged with dark-fuscous suffusion on both margins except towards base above ; in 5 a narrow irregular white suffused subcostal streak, and broad dorsal or subdorsal white streak narrowed towards base ; in J a slender white streak along upper part of termen above median streak, in ? a broader undefined patch of white suffusion : cilia in ^ pale grey, with a white basal streak on upper half of termen, in 9 almost wholly white. Hindwings rather dark fuscous, with a broad costal streak of whitish-ochreous suffusion from base to | ; cilia whitish-ochreous, in J more or less greyish- tinged, and with a grey basal line. Under-surface wholly light ochreous- yellowish, forewings somewhat infuscated ; cilia ochreous-whitish. Invercargill, in December ; three specimens taken by myself, and three others received from Mr. Philpott. I have hitherto confused this species with cethonellus, and recorded it under that name, but now see ifc to be distinct. .-Fthonellus, which is known from Mount Hutt only, has the costal edge of forewings ochreous-whitish, no white streak on upper part of termen or in cilia, hindwings without the pale-yellowish costal patch, but with cilia clear pale-yellowish except basal line, under-surface of forewings suffused with grey except towards costa and on a median streak, of hindwings partly greyish between veins. In five of the seven species of this group — viz., cethonellus, aulistes, saristes, heteranthes, and antimorus — the antennae of 3 are pubescent-ciliated — that is, clothed with short pubescence over their whole surface, but with a row of somewhat longer cilia on one side ; in the other two — melitastes and heliotes — they are glabrous (devoid of pubescence), but simply ciliated on one side. l(j Transactions. Pterophorid^. Platyptilia aeolodes, Meyr. Described (Trans. Ent. Soc. Lond., 1902, 278) from the Chatham Islands ; but Mr. Philpott has now sent me two specimens from Invercargill — a very interesting record. It is allied to falcatalis, but smaller and darker, and distinguished by the prominent angulation of termen of second segment of forewings (in falcatalis the margin is somewhat bent but not angulated), and the principal dorsal scale-tuft of hindwings being hardly beyond the middle, whereas in falcatalis it is much broader and is considerably beyond the middle. Platyptilia isoterma, n. sp. h ■I. V. y, H Face p. 33. GuDEX. — Striated Stones frovi Upper Waimakariri Valley. 33 Art. VJ. — Some Striated Stones fror)i the St. Bernard Saddle, Upper Waimakariri Valley. By M. C. GuDEX. Communicated by E. Speight. [Read before the Philosophical Institute of Canterbury, 2nd September, 1908.] Although almost all proofs of glaciatioii are frequently met with in New- Zealand, it is remarkable that the discovery of ice-striated stones has been seldom recorded. In 1904 Mr. E. G. Hogg* recorded his discovery of striated stones at Lake Wakatipu. The St. Bernard Saddle is really the terminal moraine of an old glacier which came down the valley of the Bealey over the Goldney Saddle and rounded the hill west of the Cass River. x\ll the surround- ing country bears unmistakable evidence of having been subjected to glaciation, for small lakes, roches moutonnees, moraines, and glacier- terraces are to be seen on every hand. Probably the most remarkable feature to be seen from the Saddle is a series of glacier-terraces high up on the slope of the hill to the right ; all are parallel and dip slightly to the south, thus showing the direction of the glacier's motion. The St. Bernard Saddle, which is the most characteristic moraine, is well exposed in section in a great many railway-cuttings, shingle-pits, and road-cuttings. A typical section f shows that this morainic debris has been assorted by the action of streams flowing from the glacier, for the current- bedding is well defined. The angular nature of the boulders, however, shows that they cannot have been carried fai by streams. A careful search among the stones thrown to the sides of the cuttings reveals many good speci- mens of striated stones of all sizes. They are usually composed of greywacke, but sometimes they are composed of blue slate. They possess a characteristic oval or round shape with parallel striae, and this is decisive proof of the nature of tlieir origin. The late Captain Hutton once expressed the opinion tliat few striated stones would be found in Canterbury ; but the opening-up of the shingle-pits and cuttings at the St. Bernard Saddle has exposed many good, specimens. These stones are an additional proof of the former glaciation of the Qpper Waimakariri Valley. * Trans. N.Z. Inst., xxxvii, 1904, p. 426. t See Plate I. 2— Traus. 34 Transactions. Art. VII. — On the Rarmonic Conic of Two Given Conies. By Evelyn G. Hogg, M.x\., Christ's College, Christchurch. [Read before the Philosophical Institute of Canterbury, 4th Jidy, 1908.] 1. Let two conies be taken — say, Si ^ ^hyz + 2mi2a; + 2niXy = o 8.2 ^ '2l,yz + 2m.2zx + %h^y = o. These conies are respectively the isogonal transformations of the lines Lj ^ l-i^x + m{y + n-^z = o L2 ^ I2X + 7n.2y + '>h^ = 0. The tangent to Sj at any point P will transform isogonally into a conic touching Lj at the point which is the isogonal conjugate of P. Let a common tangent to Si and S2 touch these conies in Pi and P.^ respectively, and let its equation be Xx -\- fxy -\- vz = 0. This transforms isogonally into the conic \yz + fxzx + vxy = 0, which touches Li and L.^ in the points which are the isogonal conjugates of Pi and P2 respectively. Hence, since this conic has double contact with Li and L.2, its equation is of the form L1L.2 - (px + qy + rzY = 0. Comparing this with the form Xyz + fjizx + vxy = 0 we have p- = l^l^, q- = niim^, r"- = n^n^, and this shows that the four conies which are the isogonal transformations of the common tangents of Si and So touch Lj and L^ along the four Imes y'likx ± \' yn^nioy ± s' ihu^z = 0. These four lines determine on Li and Lj eight points which are the isogonal conjugates of the points of contact of the four common tangents of Si and S2. The four points lying on Lj and the four on L, may be regarded as the intersections of Lj and Lg with a quartic curve. The equation of this quartic will be of the form LjLo [ax"" + bif^ + cz- + Ifyz + 2gzx + 2hxy) + CiC^c^Ci = 0, where c^^ v l^L^x + V-,Nj^ni.,y -}- V 11^11.2 z C.2 ^ Vy^x — V7n{m.2y — Vn^n^z Cs ^ — VI1I2X + Vviiiiuy — -/nii^z C4 ^ — %'' 1-J..2X - VniiVi.yy + \ niu^z. If we now let a = /1/2, h = miyuo, c = n{ii.2 '2f = -{m{iu + ?//oUi), 2(j =^ -{nil, + "0/1), 2// = -{lyvu^-liiih) the quartic reduces to {m{ii, - w.^ii^fy'^z^ + {nj, - nJifz-x'^ + (hni.2 - kni{)xY- + 2 [{nJ, + ^2^1) {h'>^h + y'h) xh/z + {liVi., + Imi) {m^n^ + nir/ii^ y'^zx + {m{i\, + m,n^ (n,], + nj^) zlry] = 0. Hogg. — Ou the Harmonic Conic of Two Given Conies. 35 The isogonal transformation of this — on which lie the eight points of contact of the common tangents of Si and S.^ — is the conic {m-^n^ — uuni)~x~ + {nj.;^ — nj^)'^ jf + {liVi^ — L^m^ z^ + 2 [(7?i/o+ wii) {linio + 4'?^]) y^ + (4^2 + ^Wi) {min., + niM^ zx -\-hn{ii.2 + m.^i^ {n^l.^ + yijt-^) xy] = o, which is the F conic of the two circumconics Si and S^. The form of the above quartic also shows that on the conic F He eight points which are the isogonal conjugates of the points in which the four lines VI1I2 X ± v^??JiW.2 y + ^n-{n^ z — 0 intersect the conic F^ ^ l-^L x~ + m^in., y- + ?ii"2 ^~ — ('«i"2 + m.^h) yz — ("i4 + ''-'^1) ■«'i' — (^iWa + Itni^) xy = 0. If ( ^, — , — ) and ( — , — , - ) be respectively the co-ordinates of two V /j m^ nj \ U m, nj points Oi and 0.^, then the conic F' passes through the six points in which the lines joining the vertices of the triangle of reference to 0^ and 0.2 meet the opposite sides of that triangle ; but tlaese six points are the points in which the conies 53 = \' i-^x + Vm-^y + \/niZ = 0 54 = s/lc^x -\- Vm.^j + \^n^z — 0 touch the sides of the triangle of reference. Hence the conic F^ is the F conic of S;, and S4. To obtain the equations of the four common tangents of Sj and S.j let us form the four conies Ti ^ LiLo ~ ^1^^ = 0 T2 ^ L1L2 ~ c.j'^ = 0 Tg ^ L1L.2 — C;/ = 0 T4 ^ L1L.2 — Cf = 0, and write down their isogonal transformations, which will be the equa- tions of the common tangents. Let Xo = ( ^m,7?.2 — Vm.^n^)'^, Xi = ( s^m{)h^ + '/m.My' Yo = {\/^. - W^,f, Yi = (sATJ, + V^,f Zo = i^T^i. - V'km.f, Zi = ( v'/^2 + VT^,)\ then the equations of the common tangents of the two conies Si and S2 are . ^1 ^ Xoaj + Y^y -\- ZqZ = 0 U = X,,x + Y1.7/ + Zi^ = 0 t.^ = XjA- + Yo?/ -t- Zi^ = 0 ti = Xi.c + Yi?/ + Zi^ = 0. These tangents constitute four of the group of eight lines represented by the equation (\/mi«2 + \^m^niYx + ( V'n-J,^ + Vn^liYy + ( Vl^m^ ± \ l^nii)'^ z = 0. 36 Transactions. The remaining set of four lines may be written l\ = Xja: + Yi?/ + Zi^ = 0 jj., = Xjo; + Yo' fit Pi- The isogonal conjugates of the four points in which Ci is met by the conies Ti and Pj will lie on the conic which is the isogonal transforma- tion of Cj, hence the sixteen points on F lie four by four on the four conies V liliyz + Viihm.iZX + S^iiii^xy = 0. It may be easily shown that F ^ tipi + 4 V'AjAg ( V'/iia yz + Vmjm^ zx + Vnin.^ xy) ^ hPi + 4 v^AiAa ( A//1/2 yz — VmiVi^, zx — Vn^n^ xy) ^ t-ip^, + 4 ^/AiA.2 (— \//i/.2 yz + V 7)1(111=1 z-"^ — Vnitin, xy) ^ tiPi + 4 V A^Aa (— \/ 1^1.2 yz — VviiM^ zx + V7?i«2 ^y) where Aj and A., are the discriminants of Sj and S.j. It also follows that F = i {fiPi + Lp, + t,p, + ^,:p,) = i 5 (^j;) . The conic F^ passes through the intersection of the conies lil^x^ + m{m.,y~ + n-^v.^z'^ = 0 (miWa + ?ii2^ii) ?/^ + {ihl^ -\- njj) zx + (/i?^i.2 + /.2'7ii) «?/ = 0. The former of these is the fourteen-point conic of the system of lines y IJ-i X + Vm-^m.^ y + Vn-^iu z = 0, while the latter is the isogonal transformation of the line L ^^ {^)ii{ii., + niM^ X + (?ii/2 + «oZi) y + (/i"i.2 + 'a^"!) 5r = 0. It may be at once shown that F = L'- - AjA^So where S,, is the conic x'^ y- iyl^ m{in^ n{ii.i = 0. Hogg. — On the Harmonic Conic of Tivo Given Gomes. 37 It is seen on inspection that ti+Vi = ^-2 + Ih = k-\- V-, = ii+Vi = 2L, and it is easily proved that ^{t') = 2(/) = 4 [P + 2AAA] t,t,y, = F' - 4AiA,SiS, = PilhVsPi — l^Sxyzh. It may also be noticed that the lines Li and L.^ are conjugate with respect to all comes inscribed in the standard quadrilateral '^likx + Vm^m^y ± ^n-^n.^z = o. Since t^ touches each of the conies Si and S.2 we have V^^iXq + V»hYo + x/n,Zo = 0 with similar equations of condition for t.^, t^, and ti : hence the co-ordinates of the four intersections of the conies S^ and P4 are (XoYoZo), (XoYiZ,), (X^YoZO, (XiY.Zo). The common tangents ^1, ^2, ^3, t^, are the axes of homology of the isogonal conjugates of the intersections of S3 and S4. Let the equations of two rectangular hyperbolas S' S" referred to their common self-conjugate triangle be S' ^E I'x'^ -f- m'y^ + n'z"^ = 0 S" = V'x' + m\f + h",s^ = 0. The equations of their common tangents are X Vl'i:'{m'n"-vfn') ± y Vm'm"{ii'l!' - n"l') + z x/n'n"{l'm" ~L"m') = 0. Let one of these tangents touch S' and S" at ^'{x'y'z') and '^"{x"y"z") respectively, then I'x' - k' \/l'L"{m'n" - m"n') l"x" = k" Vl'l"{m'?i" - m"n'), and therefore x'x" = k'k" {m'n" — m"n') ; similarly, y'y" = k'k" {ji'l" - n"L') z'z" = k'k" (I'no" - i",u'). Also, since V -f m' + n' = 0, I" + vi" -f 71" = 0, we have m'n" - m"ii' = n'l" - n"l' ^ I'm" - V'm' , and therefore x'x" = y'y" = z'z" — that is to say, P' and P" are isogonal conjugates. Hence the points in which the harmonic conic of S' and S" cuts those conies are isogonal conjugates in pairs with respect to the self-conjugate triangle of the hyperbolas. 38 Transactions. Art. VIII. — On certain Conic-loci of Isogonal Conjugates. By Evelyn G. Hogg, M.A., Christ's College, Christchurch. [Read bpfore the Philosophical Institute of Canterburij, 1st July, 1908.] 1. The locus of a point P (a^Sy) which moves so that the line joining it to its isogonal conjugate P' ( - 7^ - ) passes through a fixed point (ao^Soyo) \ap r/ "0 Po 70 If, however, the point (ao^Soyo) lie on either the internal or external bisector of an angle of the triangle of reference, the cubic becomes a conic and a straight line ; and the object of the present paper is to investigate certain properties which this family of conies possesses. For the sake of brevity the fixed point (ao,8oyo) through which the line joining any point to its isogonal conjugate passes will be called the centrum of the conic. The co-ordinates of the centrum are comprised in the system (o-o + 1 + 1) if we limit ourselves merely to the internal and external bisectors of the angle A of the triangle of reference ABC. The following four types of conic exist : — Centrum [a^ 11) a^ + /3y — aoa (^ + y) = 0 ... I Centrum (ao —11) a^ — /3y + aoa (/3 — y) = 0 ... II Centrum (ao 1 — 1) a' — (3y — aga {(3 — y) ■= 0 ... Ill Centrum (ao — 1 — 1) a''^ + /3y + aoa (/S + y) = 0 ... IV 2. These conies possess the following properties : they all pass through the vertices B and C of tlie triangle of reference ; those of classes I and IV pass through the ex-centres L and I^ ; those of classes II and III pass through the in-centre I and the ex-centre Ij. The tangents to the conies at I and Ii or at L and I3 pass through the centrum ; the tangents to the conies at B and C meet at the isogonal conjugate of the centrum. Hence, when the position of the centrum has been assigned, the centre of the conic can be constructed geometrically. Furthermore, the chord of intersection of any conic of this family with the circumcircle of the triangle of reference is parallel to either the internal or external bisector of the angle A of that triangle. Suppose any conic to cut the circle ABC in the points P and Q : then, since the isogonal conjugate of any point on that circle lies at infinity in a direction perpendicular to the Simson line of the point, the isogonal conjugates of P and Q will be at infinity in directions perpendicular to the Simson lines of those points — that is to say, the asymptotic angle of the conic is equal to the angle between the perpendiculars from the centrum on the Simson lines of P and Q. If the position of the chord of intersection of the conic and circle ABC is determined, the position of the asymptotes, and therefore of the Hogg. — On certain Conic-loci of Tsogonal Conjugates. 39 axes, may be found, since the centre is known, vvhile the eccentricity of the conic mav be deduced from the relation e2- 2E jj + R where R is the radius of the cu^cumcircle, and j; is the length of the perpendicular from the cii'cumcentre on the chord of intersection. 3. We now proceed to deal with certain particular conies of this family. The line f3 — y — o will meet the line at infinity in the point ib + c, — a, — a) ; with this point as centrum we have the conic a(a^ + /Sy) + (6 + c)a(/3 + y) =0 A which may be written a /3y + f3ya + Ca/3 + a {aa + b(3 -\- Cy) = 0. It is the cu'cle on IJ^ as diameter. Hence the theorem — " Any line parallel to the internal bisector of the angle A of the triangle ABC meets the circle described on I.^Ig as diameter in two points which are isogonal conjugates with respect to that triangle." The external bisector /3 + y = o meets the line at infinity in the point ih — c, —ft, ft). This point being taken as centrum, we have the conic a{a' - fSy) + {b -C)a{(i -y) ^0 B which is the circle on the line IIj as diameter. Hence the theorem — " Any line parallel to the external bisector of the angle A of the triangle ABC meets the circle described on IIi as diameter in points which are isogonal conjugates with respect to that triangle." 4. The line (S — y — o meets the circle ABC in the point ( — ft, b -\- c, Z> + c) : with this centrum we have the conic (6 +C) (a-^+ ^y) + aa(/3 + y) = 0 C. It meets the circle ABC along the line {b + C) (fta - CyS + by) + ft" (/3 + y) = 0, which may be written {b + c) (fta + 6/5 + cy) - [(/; + cf- ft-^] (/3 + y) = 0. This is satisfied by the co-ordinates of the centre of the circle ABC. Hence the chord of intersection is the diameter parallel to the external bisector of the angle A. Therefore, since the Simson lines of the ex- tremities of a diameter of a circle are at right angles to each other, we see that the conic is a rectangular hyperbola. The tangents to the conic at B and C are parallel to the internal bisector of A, hence the centre of the conic is the middle point of BC. The li)ie /3 + y = o will meet the circle KQG in the point (ft, -b + c,b - c); with this centrum we have conic ih _ ,) (a2 _ ^^) + aa (^ - y) = 0 D. Its chord of intersection with the cii'cle ABC is the diameter parallel to the internal bisector of the angle A, and its centre is at the middle point of BC. iO Transactions. 5. Let D, E, F be respectively the middle points of BC, CA, and AB : then the equations of EF, FD, and DE are — aa + hjB -\- Cy = 0 ... ... ... ... (i) Oa — b/3 + Cy = 0 ... ... ... ... (ii) aa + b/^ — cy = 0 ... ... ... .. (iii) The line ^ — y ■= o will meet the first of these lines in the point [h + c, a, a) : using this point as centrum we have the conic a(a'- + ^y) - (& + c)a(/3 + y) =0 E which meets the circle ABC along the line aa- {h + 2c) yS - (c + 26) y = o, or aa + &/3 + cy - 2 (/j + c) (^ + y) = 0. This line meets the internal bisector of angle A at the point [3(6 + c), a, a\ , which is the middle point of the line joining A to the point in which the internal bisector of A meets EF. Hence the conic is a hyperbola, whose centre and asymptotes are found in the manner previously employed. The line ^ — y = o meets the lines (ii) and (iii) respectively in the points [{b — c), a, a] and [—{b — c), a, a]. With these points as centra we obtain the conies a{a'+ f3y)~ {b-c)a{ft + y) = 0 F a{a' + (Sy) + ib-c)a(J3+y) =0 G. The former of these conies meets the circle along the line aa — b(3 — (26 — c) y = 0, which is parallel to /? + y = o and passes through the middle point of AB. The latter conic meets the circle ABC along the line aa + {b - 2c) fS - Cy = 0, a line parallel to /S + y = o and passing through the middle point of AC. Hence each of the conies F and G is a hyperbola. 6. The line /? + y = o will meet the lines (i), (ii), and (iii) of the preceding section respectively in the points [{b - c), a, -a], [{b + c), a, -a], [{b + c), -a, a]. Using these points as centra we have the conies aid" - I3y) - (b - C)a{(3 -y) = 0 H a(a--y8y) - (6 + c)a(/S -y) =0 J a{a:'- fSy)-t{b + c)a{(3-y)^0 K. Their chords of intersection with the circle ABC are respectively aa + (2c - 6) /3 + (26 - c) y = 0 aa - b/3 + {2b + c) y = 0 aa -j- (6 + 2c) p — Cy = 0. These lines are all parallel to the internal bisector of the angle A : the first of them passes through the point [3(6 — c),a, —a], w^hich is the middle point of the line joining A to the point in which the external bisector of A meets EF. The second and third lines pass respectively through the middle points of AB and AC. Hogg. — On certam Conic-loci of Isogonal Conjugates. 41 7. If the centrum be taken at the point (Oil) in which the internal bisector of the angle A meets BC we have the conic a' + (3y = o L touching AB, AC, at B and C respectively, and passing through L and I3. This conic meets the circle ABC in the line aa — c/3 — by = 0, showing that it passes through the point in which the tangent to the circle x\BC at A meets BC. This chord may also be written in the form «a + 6/3 + Cy - (i + C) {(S + y}= 0, showing that it is parallel to the external bisector of the angle A. It has real intersections with the circle ABC, hence the conic is a hyperbola. The tangents at L and I., meet at the centrum : hence the centre is the point in which the median drawn from A meets the line joining the centrum to the middle point of I2T3. The position of the axes of the conic is therefore given. 8. If the centrum be taken at the point (0-11) in which the external bisector of the angle A meets BC we obtain the conic a2-/3y=0 M which intersects the circle ABC along aa -\- bfi -\- cy — {b — c) (yS — y) = 0, a line which passes through the intersection of BC and the tangent to the circle ABC at A. The intersections of this line with the circle ABC are real if a^>4ibc, in which case the conic is a hyperbola. If a^ = 46c, the conic is a pai'abola whose axis is perpendicular to the Simson line of the point in which the above line touches the circle ABC. If a^6). Paracorophium excavatum, Stebbing in " Das Tierreich Amphipoda," p. 664 (1906). This species was originally described by Mr. Thomson from the Brighton Creek (salt water), near Dnnedin. Subsequently I took it from the same creek at a time when the water was almost fresh, and specimens lived in some of the same water for several months. I have also specimens taken from brackish water at Napier. Messrs. Lucas and Hodgkin afterwards took it near Lake Rotoiti (5 fathoms), and in Lake Waikare, where, of course, the water is perfectly fresh. It therefore appears to be one of several species of our New Zealand Amphipoda that are able to live either in salt or in fresh water. So far as I am aware, it is the only known fresh-water species of the family Corophiidce. Art. XIV. — Note on the Amphipodan Genera Bircenna, Kuria, and WandeUa. By Charles Chilton, M.A., D.Sc, F.L.S., Professor of Biology, Canter- bury College, New Zealand. [Read before the Philosophical Institute of Canterbury, 2nd December, 1908.] In 1884 I established a new genus Bircenna for a peculiar small amphi- pod found at Lyttelton. The genus was characterized as follows : Body broad, coxae very shallow. Antennae subequal, upper without a secondary appendage. Mandibles without an appendage. Maxillepedes with well- developed plates on both basos and ischios. Gnathopoda equal, not sub- chelate. Last segment of pleon and its appendages rudimentary. Telson simple, not divided. One of the most characteristic points was the greatly shortened pleon, the 6th segment being indistinct, and the telson (as I then thought) single and undivided. I left the position of the genus undecided, merely pointing out that in several respects it seemed to resemble Phlias, Guerin. The genus remained isolated and unclassified until 1899, when Mr. Stebbing placed it in the family PhUadidce — the position which it occupies in his report on the Amphipoda for Das Tierreich, though the name of the family is there written Phliantidce. In 1902, when examining the Crustacea, collected by Mr. H. 0. Forbes at Abd-el-Kuri. Messrs. A. 0. Walker and A. Scott found a small amphipod which resembled Bircenna in many respects, but differed inhaving the " telson divided to the base, consisting of two subtriangular 60 Transactions. plates set on edge." This they described as a new genus Kuria, having Bircenna as its nearest ally, and, as they were not satisfied with the position of the latter under the Phliadidce, they simply marked the genus " incertce sedis.'' Mr. Walker wrote to me at the time he was examining his Kuria, giving the points in which it differed from Bircenna, and asking for further infor- mation as to the uropoda and telson, but as my original dissection of the terminal segments of the pleon has not been preserved, and I had at the time no other specimens available, I could only refer to my figure, which showed an undivided triangular telson. In 1906 Monsieur Edouard Chevreux established a new genus Wandelia for a small r.mphipod found by the French Antarctic Expedition (1903-5) at Port Charcot and Wandel Island, which he said came very close to Bircenna, but differed from it in the uropoda, and in having the telson divided to the base. He placed the genus in the Phliantidce, which, however, he wrote Phliasidce, but pointed out that the completely divided telson separated it from all the other genera of the family. M. Chevreux apparently had not seen Mr. Walker's paper, for he makes no reference to Kuria. As Wandelia evidently resembled Bircenna even more closely than Kuria did, though like the latter it possessed a completely divided telson, I was very anxious to get further specimens to see if my original description was really correct. I did not succeed in doing this till November, 1908, when I secured another small specimen from Lyttelton Harbour, and was able to examine the point carefully. The last segments of the pleon are greatly shortened, and it is difficult to make out the exact condition of the last segment and of its appendage, but I find that the telson is distinctly formed of two parts, and is consequently in harmony with that of Kuria and Wandelia, and I therefore hasten to make the correction. So far as I can make out, each half is as deep as broad, and is triangular in vertical section as well as horizontally, and consequently the one half, which alone is shown in my figure, is nearly symmetrical when seen from above, and therefore aroused no suspicion that it was only half the telson ; and Mr. Stebbing, who dissected a specimen when preparing his generic diagnosis, published in the Trans. Linn. Soc, Zool. vii, p. 421, in 1899, seems to have been equally unaware that the telson had been incorrectly described. There can be no doubt that Wandelia is identical with Bircenna, and, indeed, Wandelia crassipes is specifically not very different from Bircenna fulva. The genus Kuria differs in a few points — e.g., in having the body laterally compressed and the 3rd uropoda less modified — and should perhaps be regarded as a separate genus, though evidently very closely alhed to Bircenna. After mentioning that Stebbing had placed Bircenna in the family PhliantidcB, Walker says that " it seems somewhat out of place with such genera as Pereionotus, Iphinofus, &c." In general appearance it certainlv looks very unlike these dorso-yentrally flattened genera, and Kuria, which is somewhat laterally compressed, is still more unlike them, and both genera differ from the rest of the family in having the telson double or deeply cleft. In other respects, however, they agree closely with Stebbing's diagnosis of the family. The genus Phlias, from which the family takes its name, also differs greatly in general appearance from the genera named above, and resembles Kuria in having the body somewhat laterally compressed ; but, as a small amount of lateral compression in the one case and of dorso- ventral compression in the other make the general aspect of the two forms Chilton. — Amphipodan Genera Bircenna, Kuiia, and Wandelia. 61 very different, it is probable that comparatively little importance should be attached to this point. The possession of a double telson is more important, and distinctly marks these two genera off from the rest of the family ; but this seems to me to point rather to the necessity for slightly enlarging the characters of the family than for the establishment of another family, and I therefore leave the two genera under the Phliantidce, where Chevreux placed his Wandelia. In both species of Bircenna — i.e., B. fulva and B. crassipes— the pleopoda have the peduncle broad and laterally produced, as in other members of the family. I give below the arrangement I suggest for these forms, with the characters that appear to me most important for differentiating them. I have shortened the diagnosis of Bircenna, as that given by Stebbing in " Das Tierreich Amphipoda " appears to me to include some details that are hardly likely to prove of generic value ; indeed, some of them have to be omitted to include the second species {B. crassipes). The characters given are, of course, additional to those of the family, and these have not been repeated in the generic diagnoses. Fam. PHLIANTID.E. Phliadidre, Stebbing in Trans. Linn. Soc, London, ser. 2, vol. vii, p. 414 (1899). PJdiantidce, Stebbing in "' Das Tierreich Amphipoda." p. 200 (1906). Genus Bircenna, Chilton. Bircenna, Chilton in Trans. N.Z. Inst., vol. xvi, p. 264 (1884). Bircenna, Stebbing in " Das Tierreich Amphipoda," p. 205 (1906). Wandelia, Chevreux in Exped. Antarctique Franjaise, 1903-5, " Crustaces Amphipodes," p. 44 (1906). Body broad, almost cylindrical, pleon segment 5 very short, 6th indis- tmct. Side-plates all very shallow. Maxillipedes with inner and outer lobes long, both reaching apex of 2nd joint of palp, which, though short, contains 4 joints. Gnathopoda 1 and 2 slender and almost simple, similar. Perpeopods short, the 3rd to 5th with the 2nd joint much expanded, and the 4th joint rather expanded and decurrent. Uropoda short, 3rd uni- ramous, lamelliform, peduncle and branch not clearly distinguishable. Telson split to the base, each half subtriangular. 1. Bircenna fulva, Chilton. B. fulva, Chilton in Trans. N.Z. Inst., vol. xvi, p. 264, pi. xxi, figs. 1, 1 a-e (1884). B. fulva, Stebbing in "Das Tierreich Amphipoda," p. 205 (1906).. Gnathopods similar, not longer and only slightly more slender than the 1st and 2nd pera?opods ; 3rd joint longer than broad, as long as 4th ; 5th a httle shorter than the 6th, which is not expanded, but a little produced at apex, yet not enough to make a chela with the short apically toothed finger. Uropod 1 with peduncle much shorter than the acute curved rami, outer ramus much shorter than inner ; uropod 2 similar, but stouter and shorter; uropod 3 apparently consisting of a single joint, bifid at end, outer apex rounded and bearing a few setse, inner pointed and with only one or two setce. Telson, each half subtriangular, but with apex broadly rounded, with a small seta on each half. Length, 3 mm. Lyttelton and Otago Harbours, New Zealand. 62 Transactions. 2. Bircenna crassipes (Chevreux). WandeTia crassipes, Chevreux in Exped. Antarctique Franyaise, " Crustaces Amphipodes," p. 45, figs. 24-26 (1906). Similar to B. fulva except in the following points : Gnatliopods longer and mucli more slender than 1st perjeopod. Uropods 1 and 2 with rami subequal and only sUghtly longer than peduncle. Telson completely divided into two triangular lobes, each armed with a small seta. Length, 3 mm. Port Charcot (dredged at depth of 40 metres), Wandel Island (dredged with sponges in 40 metres). Bircenna fulva. Fig. 1. — Third pleopod ; liighly magnified. FiG. 2. — Uropoda and telson (side view) ; highly magnified. Fig. 3. — Telson and 3rd uropoda (from above) ; highly magnified. Genus KuRiA, Walker and Scott. Kuria, Walker and Scott in Nat. Hist. Sokotra, p. 228 (1903). Body laterally compressed. Side-plates not very shallow, the first 4 as deep as their segments. Maxillipedes with inner and outer lobes very small, especially the latter ; neither reaching further than base of 2nd joint of the 4-jointed palp. Gnathopods 1 and 2 subequal, long and slender, with a small subchelate palm. Perfeopods short, last three with 2nd and 4th joints expanded. Uropod 3 with single ramus. Telson divided ta ttie base, consisting of 2 subtriangular plates set on edge. Chilton. — Ampliipodan Genera Bircenna, Kuria, and Waodelia. 63 1. Kuria longimana, Walker and Scott. Kuria longimanus, Walker and Scott in Nat. Hist. Sokotra, p. 228, pi. xivh, figs. 5-5n (1903). K. longimana, Stebbing in " Das Tierreich Amphi- poda," p. 726 (1906). Body rather plump, first 4 side-plates deeper than their segments ; last 3 segments of pleon coalesced. Gnathopods very slender, 2nd joint as long as the next 3, 5th as wide and almost as long as the 6th, which is about 5 times as long as broad ; palm very small, oblique, defined by a spine, finger projecting beyond palm by about one-fourth of its length. Uropods 1 and 2 with peduncles rather shorter than the rami, which are equal and similar, and bear a few spines ; 3rd uropod with peduncle short and broad, the single ramus about as long as peduncle, but more slender, and with one or two spines at apex. Telson divided to base, the two subtriangular divisions turned up on edge, the lower margin being convex and the upper straight, with 2 or 3 setse near the distal end. Length, 2 mm. Abd-el-Kuri. Remarks. In addition to the points that have been mentioned in the descriptions given above, there are several others that I have not included, because I have not yet been able to make a satisfactory comparison of them in the different forms. For example, Messrs. Walker and Scott describe the last 3 segments of the pleon as being fused together in Kuria longimana ; and Chevreux says that the last 2 segments are fused together in Bircenna crassipes. They appear to be fused also in B. fulva, but owing to the imperfect development of the 6th segment it is difficult to be quite clear as to the actual state of affairs. In Bircenna crassipes, as figured and described by Chevreux, there is no molar process on the mandible, while in Kuria longimana Messrs. Walker and .Scott describe the molar process as " rather large." In Bircenna fulva the mouth parts, so far as I have been able to examine them in the single very small specimen at my disposal, appear to closely resemble those of B. cras- sipes. The mandible shows no molar process or palp, the cutting-end is formed of some 4 or 5 indistinctly marked teeth, and the accessory process is either absent altogether or very imperfectly developed. The 2 pairs of maxillte have practically the same form as in B. crassipes, and the maxilU- pede also closely resembles that of the same species. The upper Up is small, and regularly rounded at the end, which bears a few very short setae ; in the lower lip the lateral lobes are rounded and finely ciliated on the distal border. The 3rd pleopods are shown in fig. 1. They have the inner margin of the peduncle much produced, and bear 2 very short coupling-spines at its distal end ; the inner branch has a projection of its outer margin near the base, as shown in tlie figure. The other pleopods closely resemble the 3rd pair. 64 Transact 107}$. Art. XV. — The Geology of the Quartz Veins of the Otago Goldfields. By A. M. FiNLAYSON, M.Sc, A.O.S.M. Communicated by Dr. Marshall. [^Read before the Otago Institute, \-iih July. 1908.] Introductiox. The accompanying paper contains the results of investigations into the geology of the veins of the Otago Goldfield. The area is a large one, and the paper is not exhaustive, but the different ty^es of veins have been ex- amined, and the features of every group described and discussed. As most of the mines are now closed down, the district is not an ideal one for studying vein-phenomena, and it is to be regretted that the work was not undertaken many years ago, when Bullendale, Bendigo, and the O.P.Q. workings were accessible. I wish to acknowledge my great indebtedness to Professor Park, Dr. Marshall, and Mr. D. B. AVaters, of the Otago School of Mines, for much help and advice, both in the field and in the laboratory ; and to Mr. A. 0. Bishop, of Skipper's, and Mr. R. Mollineaux, of Barewood, who gave me great facilities in examining their mines. General Description of the District. The Otago Goldfield, as far as veins are concerned, embraces an area of nearly 10,000 square miles, stretching from Lake AVakatipu on the west to the sea-coast on the east, and from Cardrona in the north to La^\Tence in the south. This district is drained chiefly by the Ciutha and Taieri Rivers, and also by the smaller Shag River. The country is mountainous, the various ranges running for the most part approximately north-east and south-west, or at right angles to the course of the Kawarau River, while the tributary streams flow between and parallel to the ranges. This disposition is described and discussed by Dr. Marshall in his " Geography of New Zealand."* Professor Park claims that the ranges of Central Otago are block mountains.! The climate of the inland districts is much hotter in summer and colder in winter than on the east coast, but the rainfall is generally low. For this reason the hills and valleys are practically barren of vegetation, being clothed only in tussock. Dearth of water and absence of timber are serious hindrances to mining in some parts of the field. The goldfield has no centre of population, but "comprises a number of towns which grew up in the roaring days of alluvial mining, for which the district is chiefly noted. The principal towns are situated on the Ciutha River, or in its drainage-basin, and stand as fingerposts indicating the ♦Marshall, "Geography of New Zealand" (Whitcombe and Tombs, 1905), p. 102. tPark, Bull. No. 2, N.Z.G.S., 1906, p. 7; Bull. No. 5, N.Z.G.S., 1908, p. 9. FiNLAYSON. — Geoloyy of Quartz Veins of Otago Goldfields. 65 march of the pioneer diggers from the coast inland. Communication, which in the early days was difficult, is now good, the most remote mining districts being connected by coach and rail with Dunedin. Previous Geological Work. The geology of the district has been the subject of a good deal of notice, and a complete bibliography is given in Bulletins Nos. 2 and 5, N.Z. Geological Survey (New Series). The quartz veins have, how- ever, not been much studied, the chief works being by Ulrich, Rickard, and Park. The following list includes all work written on the Otago veins : — McKay, Alexander — "Carrick Antimony Lodes." Geol. Explorations, 1882, p. 80. "Antimony on Barewood Run," Geol. Explorations, 1890, p. 54. "Qiiartz Reefs at Nenthorn," Geol. Explorations, 1890, p. 50. 3— Tran--. 66 Transactions. Park, James — "Green's Reef, Ophir." Geol. Explorations, 1888, p. 17. " White's Eeef. Old Man Range," Geol. Explorations. 1888, p. 32. Alexandra Antimony Lode," Geol. Explorations, 1888, p. 33. " Economic Geology of the Alexandra Sheet," Bull. No. 2, N.Z.G.S., 1906, p. 21. Rickard, T. A.— "Goldfields of Otago," Trans. Am. Inst. Min. Eng., vol. xxi, p. 411. Eowe, W. E.— "Antimony Lode at Hindon," Geol. Explorations, 1879-80, p. 153. "Antimony Lode, Waipori," Geol. Explorations, 1879-80, p. 155. "Waitahnna Copper Lode," Geol. Explorations, 1879-80, p. 156. Ulrich, G. H. F.— "Goldfields of Otago": Dunedin, 1875. " Handbook of New Zealand Mines," 1887, 1906. Geology of the Goldfield. (a.) Geological Formations. The main formation of the goldfields and the country rock of the veins is a foliated schist of considerable thickness. It varies locally, but for the most part it is a mica-schist, more or less quartzose, and only submeta- morphic in its upper portions. The schists have been described by Hutton as forming an anticline whose axis runs south-east from Lake Wakatipu to Dunedin, with a syncline on either side of it.* Along the axis of the anticline, where denudation has been most active, are exposed the lowest and most metamorphic beds, while younger and semialtered slates and phyllites are preserved in the adjacent synclines. As we pass north-east or south-west we come on younger rocks (conglomerates and greywackes), and -finally reach fossil- iferous beds at Kurow in the north-east, and in the Hokonui Hills in the south-west. The former have been classed as Permo-carboniferous,t and the latter as Triassic and Jurassic. J The age of the schists has as yet been little more than guessed at, and no systematic attempt has been made to ascertain their relation to the above fossiliferous beds. The quartz veins are confined to the schistose rocks, but this is evidently an effect of the distribution of the fissuring-force. and not due to a different age of rocks. It will be sufficient at present to regard the gold-bearing series as of middle and upper Palaeozoic age. The schists are traversed by a number of structural faults, running for the most at right angles to the axes of the folds described by Hutton, or north-east and south-west. The faults have been mapped by McKay ,§ and described later Ijy Park.|| It is open to question, however, if they are so dominant and easily traced as these writers claim. This much seems evident — namely, that the schists are much faulted, and that the faults have roughly the direction stated. * Hutton, " Geology of Otago," 1875, p. 30. t Park, " Permo-carboniferous Rocks at Mount Marv," Trans. N.Z. Inst., vol. xxxvi, p. 447. $ Hector, '^ Outline of New Zealand Geology" (Wellington, 1S86), p. 83. § McKay, " Older Auriferous Drifts of Central Otago"' (Wellington, 1897), p. 107. II Park, Bulls. 2 and 5, N.Z.G.S., 1906, 1908. FiNLAYSON.— Geo/o(/?/ of Quartz Veins of Otago Goldfields. 67 For a goldfield, the district is poor in igneous intrusions. An outcrop of actinolite-schist near Ophir is probably a metamorphosed dyke.* There are, at Gibbston and Moke Creek, outcrops of serpentine-talc rock, repre- senting magnesian intrusives of doubtful age.j Finally, there is the im- portant middle Tertiary series of volcanic rocks developed especially round Dunedin, and along the east coast as far north as Oamaru and inland to Macrae's.J The rugged and little-known district between the lakes and sounds doubtless contains extensive igneous intrusions, as judged from pebbles picked up in the Clutha and Kawarau Eivers. . The next formation, chiefly developed along the coast, is the Tertiary limestone series of New^ Zealand, seen as a small patch at Bob's Cone, near Queenstown, where it has been preserved from denudation by being involved in a fault-line in the schists. Then follow the Pliocene auriferous gravels and cements, shales, and sands, which fill the valleys of the goldfield (formerly old lake-basins), and finally the Pleistocene river and lake terraces, for the most part auriferous. (b.) Geological History. As far as we know at present, sedimentation was continuous, with minor breaks, from the middle Palpeozoic, and perhaps earlier, till near the end of the Jurassic period. During this extended time a vast thickness of sedi- ments was deposited. Then followed, throughout the South Island, the main upheaval of all these older beds, accompanied by the intrusion of an important belt of granitic rocks, which can be traced from Nelson, through Westland, and probably through western Otago, down to Preservation Inlet and Stewart Island. At the same time the metamorphism and alpine folding of the older rocks was mainly effected. With elevation, denudation became active, and the younger Mesozoic beds were removed from the central portions of Otago, where the uplift was greatest. Subsidence followed in the early Tertiary, and a series of coals and lime- stones was deposited, the sea extending far into the interior. Then followed elevation, accompanied by faulting and volcanic activity. Denudation at the same time almost entirely removed the Tertiary deposits, and the pre- sent drainage-system of Otago was inaugurated. Subsequent movements are not quite clear, but there probably occurred a Phocene depression, during which the deposits of the Central Otago lake-basins were laid down, followed by a late Phocene and early Pleistocene elevation, accompanied by glacial extension, and then a subsidence, with retreat of the glaciers. The Veins. With some exceptions, the veins are small, rarely exceeding 2 ft. or 3 ft. in width. The filling is largely crushed and altered rock, accompanied in the smaller ones by veins and stringers of quartz, and in the larger by lenses or blocks of quartz, varying in size. The predominant ore is gold, with very little silver (fineness, 960), ac- companied by auriferous pyrite. Other minerals are scheeUte and stibnite, which are common, and sometimes constitute the dominant ore ; also galena, bournonite, and zincblende, which are rarfe. * Park, Bull. No. 2, N.Z.G.S., 1906, p. 41. t Finlayson. " Notes on the Otago Schists," Trans. N.Z. Inst., 1907, p. 76. j Marshall, " Geology of Dunedin," Quart. .Journ. Geol. Soc, vol. Ixii, p. 422. 68 Transactions. There are, in addition, two small copper-veins and one cinnabar-vein. The veins may be divided into groups according to their locality and characteristics, as follows : (1) Glenorchy, (2) Skipper's and Macetown, (3) Carrick Range, (4) Bendigo, (5) Macrae's, (6) Waipori, (7) Barewood, (8) copper- veins, (9) cinnabar-vein, (10) barren reefs and fault-fractures. (1.) Glenorchy Veins. The chief vein in this district is a scheeUte-bearing vein, which I have ■described in a previous paper.* (2.) Skijiper^s and Macetown Veins. The veins of this district are mineraUsed shear-zones rather than flssu^re- veins. The country rock is a soft, finely laminated mica-schist, traversed by broad belts of fracturing. Along these belts the rock is sheeted or divided by several parallel fissures, the intervening schist being crushed and con- torted, and more or less altered. These planes of fracture served as channels for the mineralising solutions, which caused the formation of segregated lenses or blocks of quartz. These blocks are of varying size and value. The gold is mostly fine and free, and the adjacent shattered schist or lode- formation is impregnated ^N-ith ppite. The Shotover, or Nugget and Cornish, Vein. — The country rock strikes north and south, and dips to the west at from 30° to 45°. The vein, striking north-west and dipping south-west at about 60°, crosses the Shotover River about two miles above Skipper's Point. At the river-bank there are two veins, the eastern and the western, about 100 ft. apart. These two merge into one a short distance up the hill, and the single fissure-Une has been traced across the ranges for some miles to the north-west. On the south- east side of the river the two outcrops are distinctly seen, but only the eastern has been traced for any distance. This runs over the dividing-range, ap- parently in hne with the Premier reef of Macetown. The vein is typical of its class, two main fractures constituting respectively the hanging and foot walls, wdth a parallel sheeting of the intervening belt by subordinate fractures. In the western reef four blocks of quartz have been stoped out. At the junction of the two veins a large block (the No. 1) was stoped for a depth of 250 ft. below the surface. The blocks are generally lens-shaped, and hmited on all sides. They are generally bounded by thin clay partings or selvages, but not infrequently these are absent, and there ~ ' h f! Fig. 1. a. Quartz shoot, h. Veiu-fonuatiou of cruslied schist. is a gradual transition from quartz to lode formation. In such cases the quartz " makes" gradually out of the lode-formation, and passes over to a parting or wall, where it wedges out (fig. 1). *Finlayson, " Scheelite-deposits of Otago," Trans. N.Z. Inst., 1907, p. 110. Fi'SLAYSON. ^Geology of Quartz Veins of Otago Goldfields. 69 The lode-formation varies in width from 8 ft. to 20 ft., and has generally defined walls with tough clay casings. The value of quartz varies from 5 dwt. to 20 dwt. per ton. The gold is fine, hackly, and free, the extraction being about 80 per cent, by mill amalgamation. The pyrite is auriferous, but not by any means rich enough to warrant the treatment of the pyritic lode-formation, as some promoters would have us believe. In places, more especially near the surface, the lode-formation contains bands of a soapy yellowish-grey rock, especially near quartz, and devoid of pyrites. The following analyses indicate the normal mode of alteration : — H.O SiOa Al.Os Fe^Os FeO CaO MgO KgO Na.,0 Mnb TiO, CO., FeS., . 1. 2. 3. 4. 2-06 2-48 2-13 -f- 0-07 53-05 54-12 46-30 — 6-75 10-31 11-94 10-31 9-74 5-63 4-83 — 4-91 8-60 6-54 5-60 — 3-00 5-17 3-93 3-37 — 1-80 0-72 1-65 1-41 + 0-60 4-74 4-73 4-05 — 0-69 2-90 4-31 3-69 + 0-79 0-51 0-22 0-18 — 0-33 1-06 0-39 0-32 — 0-74 1-15 1-51 1-30 + 0-15 3-43 2-94 + 2-94 100-01 100-88 86-43 + Unaltered country rock. Altered lode-formation. 4-64 18-22 -13-58 Altered lode-formation, recalculated on a basis of constant alumina. Gains and losses of altered rock. These figures show — (1) that a good deal of replacement has occurred injconnection mth the segregation of quartz ; (2) that the type of rock- alteration may be regarded as partial sericitization. ■ The following analyses indicate the nature of the yellowish altered rock : — 1. 2. .3. 4. H,0 2-06 2-60 1-56 - 0-50 SiO., . 53-05 46-90 28-14 —24-91 Al,63 . . 10-31 16-46 10-31 Fe,0, . 9-74 6-67 4-00 - 5-74 FeO 8-60 7-26 4-35 - 4-25 CaO 5-17 7-45 4-47 - 0-70 MgO 0-72 1-97 1-18 -1- 0-46 K^O 4-74 4-07 2-44 — 2-30 Na.O 2-90 2-08 1-25 — 1-65 Mnb 0-51 0-23 0-14 — 0-37 TiO. 1-06 0-27 0-16 - 0-90 CO.; 1-15 3-98 2-19 + 1-04 FeS^ . 99-94 100-01 60-19 + 1-50 1. Country rock. -41-32 2. Yellow rock. - 3. Yellow rock, recalculated ^\^th constant alumina. -39-82 4. Gains and k )sses. 70 Transact20?is. It is evident from these figures that this altered rock is a kaoUiiized variety of the normal lode-formation. The bleaching and the total removal of pyrite are probably due to the secondary processes of descending surface waters, accompanied by the formation of kaolin. Present mine-workings have not yet shown what factors regulate the occurrence of the quartz blocks. It is probable, however, that they are connected with some local structural features. The No. 1 block, for instance, occurred where the two reefs junction. A common occurrence of gold in this and other veins of the district is as fine " paint " coating the clay selvages. This is probably due to pro- cesses of secondary enrichment, the clay partings acting as a filter to the gold-bearing solutions. In other words, this seems to be an instance of adsorption- — the process recently studied by Kohler.* Microscopically the quartz occurs in coarse granules, with patches of fine-grained quartz studded with pyrite crystals. Such patches evidently indicate portions where replacement has occurred. Other Veins. — The Invincible, fifteen miles up the Rees Valley from Glenorchy ; the extensive group of veins round Macetown ; some veins near Arrowtown ; and the BuUendale or Phoenix vein, up Skipper's Creek, as well as other smaller veins in the Shotover Basin, all belong to this type, and have the same characteristics. (3.) Veins of the Carrick Range. The northern flank of the Carrick Range, overlooking the Bamiockburn Flat, is intersected by a complicated system of small veins, striking in various directions. The country rock is a mica-schist of varying type, striking north and south, and dipping to the east. The eastern flank of the range is bounded by a well-marked fault, which passes near the veins and drags down the schist with it, the rock along the fault-hne standing almost verti- cally. The veins, which are irregular and considerably disturbed, vary in width from 18 in. to 3 ft., and the filling consists of mullock or highly crushed schist, impregnated with pyrite, and traversed by stringers of gold-bearing- quartz. Ulrich referred the irregularities of the veins to disturbances caused by the intrusion of supposed dykes of " hornstone-porphyry."t As I have shown elsewhere,! these dykes do not exist, and both Hutton and Uhich made a peculiar mistake in failing to identify the horny sihcified gossan of some of the vein-outcrops. The map of the Carrick Range veins shows the interesting system the individual members of which have been described in detail in Bulletin No. 5, N.Z. Geological Survey. They fall naturally into four groups — the Cale- donian, Carricktown, Young Australia, and Antimony groups. 1. The Caledonian Group. — The veins of this group, the most northerly of all, occupy a radiating group of fissures, varying in strike from north and south to north-west and south-east. They dip at high angles. 2. Carricktown Group. — These veins, which occur near old Carricktown, also form a similar radiating group, opening out, however, towards the north and west, whereas those of the Caledonian group spread out to the south and east. * E. Kohler, " Zeitschrift fur Pi-aktische Geologic," 1903, p. 49. t Hutton and Ulrich, " Geology of Otago," 1875, p. 162. I Finlayson, " Notes on the Otago Schists," Trans. N.Z. Inst., 1907, p. 72. FiNLAYSON. — Geology of Quartz Veins of Olago Goldfields. 71 3. Young Australia Group. — This comprises a number of flat-dipping veins lying for the most part to the south of the last group, and crossing the country rock both in strike and dip. They occur only on the higher slopes of the range, having evidently been denuded off the lower parts. The Border Chief, Heart of Midlothian, and Vale of Avoca veins, lying on the high spur west of the Caledonian group, are also members of this group, the ridge not having been sufficiently denuded to remove them. 4. Antimony Group. — The veins of this group are similar in character to the others, but they carry bunches of stibnite besides being auriferous. They occur in a scattered group on the summit of the range, to the west of and distinct from tlie other groups. CARRICK VEINS. Scale : 50 chains to an inch A M. Fxnlaysun Gold veins . Antimony veins : The Fissure-system. — The somewhat complicated system seems to be best interpreted as follows : There have been two sets of radiating fissures formed — the Caledonian and the Carricktown. Their formation was doubt- less due to torsional stress, and the features of these groups are very well reproduced by Daubree's experiments on the fracturing of glass by torsional effects.* There has also been a shearing movement, which resulted in the formation of the flat-lying fissures of the Young Australia group. To this movement are probably due many of the disturbances in the other veins, such as the peculiar horizontal displacements which have affected some of the veins. * Daubree, " Geologie Experimentale," 1879, p. 306. 72 Transactions. The fault-lines in all the veins are gold-bearing, and often carry thin stringers of quartz. Unless this is due to secondary enrichment, the filling of the fissures must have extended over a considerable period of time. The order of movement seems to have been : (1) Formation of radiating fissures ; (2) formation of flat fissures or shear-planes, with disturbance of the radiating fissures ; (3) final adjustment of the fissured area, with faulting of the flat fissures. In other words, the evidence seems to indicate that the formation of the radiating fissures was the cause of all the movements which followed, these latter being due to forces called into play to readjust the strain on the fissured area. The formation of the fault on the east flank of the range, which was subsequent to and independent of these local movements, also doubtless disturbed the veins, but it is not possible to say to what extent. Localisation of Ores. — A striking feature is the occurrence of the antimony- ore limited to the extreme west of the fissured area, no more than a trace of antimony being found in the sulphide minerals of the other veins. This is evidently due to processes of ore-segregation beneath. Gold. — In the oxidized zone, which extends to a depth of about 60 ft., the gold is free and easily extracted, and from a comparison of the very high values which have been obtained on the surface with the much lower value of the unoxidized ore it is evident that an immense amount of secondary enrichment has taken place. The unoxidized ore is impregnated with a sulphide having by analysis the empirical formula FeAsgSg, evidently a mixture of iron and arsenical pyrites. J. S. Maclaurin recently made a series of extraction tests on samples of quartz from the Carrick Range,* mth the following results : Fire assay — Gold, 17 dwt. 8 gr. per ton ; silver, 3 dwt. 3 gr. per ton. " No gold was visible in the stone, but panning-ofF showed a little free gold." Amalgamation — Extraction, 55 per cent. Chlorination without previous roasting, 33 per cent. Cyanidation, 62-7 to 72*3 per cent. Cyanidation with subsequent amalgamation, 9r3 to 96"4 per cent. These results indicate that the gold is largely associated with sulphides, partly as a coating, most of which amalgamation would remove, and partly involved in the sulphides, which explains the small extraction from un- roasted ore by chlorination. With a lens a little free gold can always be seen in the quartz, and much more coating the sulphides in irregular strings. Stibnite. — This is highly crystalline, often shows a marked comb-structure parallel ■with the vein- walls, and is rather quartzose and low-grade. It occurs in bunches easily freed from the soft lode-formation (at least, in the oxidized parts), but requires much dressing to make it marketable. Similar Groups of Veins. — The Old Man Range, near Alexandra, carries on its flanks a number of small veins similar in character to those of the Carrick Range. White's reef is the best -known. It is significant that a small antimony-vein occurs at Alexandra, thus completing the parallel between the two groups of veins. (4.) The Bendigo Veins. The veins of Bendigo lie on the north-w^est flank of the Dunstan Range, three miles from the Clutha River. The country rock is a firm and highly plicated quartz-mica-schist, lying almost horizontally. The veins, which are small and narrow, occupy a series of well-defined parallel fissures running * Government Mines Report (Wellington, 1905), p. 9. FiNLAYSON. — Geology of Quartz Veins of Otago Goldfields. 73 east and west, and standing almost vertically. These are well shown on the plan, and it will be seen that there is also a subordinate series of diagonal veins crossinsr them. The lode-matter consists of crushed and altered schist, impregnated with pyrites and traversed by defined and continuous seams of quartz, which may run on either or both walls, occasionally occupying the whole width of the vein, with frequent splits and branch stringers. The quartz seams often show a very fine comb-structure. In the upper levels the ore was oxidized, and extraordinary values were frequently obtained from small patches near the surface. In depth' the ore is reported to be refractory, and sulphides — pyrite, galena, and blende — become prominent. The individual veins have been described in detail in Bulletin No. 5, N.Z. Geological Survey. The group also includes the Alta scheelite-vein, which lies about three miles to the east of the main grouj). This seems another instance of the segregation of ores. ^'^ct.^ O* BENDIGO VEINS Surveys by G. F. Hosking Si-u/f o/ Chains. Bee Vein Hit or Miss Vein The Si/stem of Fissures. — The Bendigo group illustrates the sheeting of rock by fissures, discussed many years ago by Emmons in his " Structural Relations of Ore-deposits.''* It is also noteworthy that the best ore was largely obtained from the neighbourhood of intersections wath the cross- fissiires — an instance of ore-shoots at intersections. The minor cross-veins, in fact, besides being payably auriferous, served as reliable indicators. At the intersections a mutual displacement frequently occurred — a phenomenon characteristic of crossing fissures, even when formed simultaneously. The cross-veins are doubtless the result of shearing stresses set up in the rock at the time of formation of the main fissures, the compound fissure- lines being opened in such directions as would best relieve the strain. * Enimous, " ScructuvAl Relations of Ore-depo iits," Trans. Amer. Inst. Min. Eng., vol. xvi, p. 821. 74 Transactions. The Vem-fiUing. — The quartz shows throughout a distinct banding, parallel to the vein-walls. The crystal-axes of the quartz are distinctly seen at right angles to the banding, and frequently very fine cavities with comb -structure are to be seen (Plate II, la). Brecciation is common, the quartz cementing fragments of country rock impregnated with pyrites, and indicating that movement occurred subsequently to the first mineralisa- tion of the fissures (Plate II, lb). Chemical tests and microscopic examination of the sulphides show that the habit and association of the gold is very similar to that of the Carrick Range. The quartz, according to Ulrich and to the statements of miners, occurs in shoots dipping east along the strike of the veins. This is a matter which cannot be investigated at present, as the old workings are all closed. The very high values which have been picked up near the grass on several of the veins are evidently the result of prolonged secondary enrichment. Microscopically the ore is seen to be banded in alternate lines of coarse and fine granules, and carries also bunches of fine granular quartz thickly studded v.dth pyrite crystals (Plate II, 2.) Professor Park calls the Bendigo veins " immature replacement lodes,''* but the highly drusy and crustified nature of the quartz frequently observed argues rather for fissure-filling, and is a decided argument against Professor Park's theory. The deepest workings in Otago were on this group, the Cromwell shaft having been sunk to a depth of 500 ft. Other Veins allied to the Bendigo Veins. — The Conroy's Gully vein, near Alexandra, is similar to these or to the Carrick veins. The group of small east-and-west veins at Rough Ridge, now almost forgotten, are very similar to the Bendigo type.f Lastly, the Nenthorn group, J east of the Taieri Gorge, whose exploitation lasted for a period of two years, from 1889 to 1891 , may be put under this heading. They comprise a similar set of narrow parallel veins, striking east and west, and dipping either north or south at a steep angle. (5.) Veins of Macrae's District. These are an important group of scheelite-veins, which I described in a previous paper.§ They are typical bedded or segregated veins, being the only group of this nature in Otago. (6.) Veins of Waipori and Southern Districts. Ulrich has described four of these veins — the O.P.Q., Canada, Gabriel's Gully, and Saddle Hill veins. || He states that they are characterized by shoots or blocks of quartz which " show an endlong dip in strike." The feature, he says, " may be considered as an oblique banded structure on the large scale," the banding being marked by alternate blocks of quartz and mullock. He also remarks that the gold occurs in shoots in the quartz blocks, in the centre or on either wall. The O.P.Q. {Otago Pioneer Quartz-mining Company's), or Shetland, Vein. — This vein, near Waipori Township, strikes at about 160°, and dips eastward at an angle of 56°. The country rock is a slaty quartz-schist, striking north- * Park, Bull. No. 5, N.Z.G.S., 1908, p. 63. t Ulrich, " Geology of Otago," 1875, p. 229. j McKay, Rep. N.Z. Geol. Explorations. 1890, p. 50. §rinlay.son, " Sclieelite-deposits of Otago," Trans. N.Z. List., 1907, p. 112. II Ulrich, " Geology of Otago," 1875, pp. 159, 191. FiNLAYSON. — Geology of Quartz Veins of Otago Goldfields. 75 east and dipping south-east at an angle between 10° and 25°. The walls are fairly defined with seams of gouge, and the vein has been opened up for nearly two miles along the strike, but the workings are now inaccessible. Its thickness varies ; in places it is no more than 2 ft., but the average distance between walls is about 10 ft. The rusty quartz from near the surface was in patches extremely rich, while the deepest levels (200 ft.) averaged from 7 dwt. to 12 dwt. per ton. The quartz is, in general, seamy, and distinctly banded by parallel streaks of pyritic matter. The quartz shoots may occupy the whole width of the vein or only a short width on either wall. The dip of the shoots is regular and characteristic, although they generally wedge out in lens fashion when followed down, to make again on the same track at a greater depth. Microscopically the quartz is mostly fine-grained, with occasional coarse granules enclosed in it, giving a pseudo-porphyritic structure. Frequent strings and veins of calcite are present, and the mass of fine-granular quartz is crowded with pyrite. Evidently the quartz is very largely a result of replacement, and the very distinct banding occasionally seen is best ex- plained as due to progressive replacement of sheeted rock by ore. In general the vein bears strong resemblances in structure to those of Skipper's and Macetown. A fuller description is given by Mr. T. A. Rickard in a very graphic article.* Canton Vein. — This is similar to the last. It lies close to that one, and strikes in a direction to join it, the probable junction lying in a gravel-filled basin. These two veins in their field-relations may be compared with the tAVO branches of the Nugget and Cornish vein. Bella Vein. — This lies four miles from Waipori Township, in Long Gully, a branch of the AVaipori River. It strikes east and west, and stands almost vertically. It has fairly defined walls, and varies from 3 ft. to 5 ft. in thickness. Where exploited, it consisted at the surface of a shoot of payable quartz from wall to wall. This block was stoped out for a depth of 50 ft. when it ran over to one wall and wedged Ym. 2.— Section of Bella Vein, o^it, although the width between walls was maintained. The vein carries a little scheel- ite, which is found in some quantity in several little-known veins in this district. Cox^s four miles from Waipori in a northerly direction. On the line of fissure, Vein. — This lies on the flanks of the Lammerlaw Ranae, about o^> Vci )i F/S3' Fig. 3. — Sketch-plan of Cox's Vein. which strikes about east and west, and stands vertically, two shoots of stone were opened out on the surface, dignified by the names '• Maori " and " Maud," with a contraction of the fissure between them. * Rickard, " Goldfields of Otago," Trans. Amer. Inst. Min. Eng., vol. xxi. ]>. 416. 76 Transactions. On the Burnt Range and Lammerlaw Range there are a number of small veins or leaders, some carrying good gold. Their strike is for the most part east and west, and they dip in either direction, with varying underhe. They show similar characters to the O.P.Q. — namely, the occurrence of lenses of quartz in the fissure-zone. The smaller veins, however, carry generally a stronger and more continuous body of quartz than the larger. Waifori Antimony -vein. — This occurs on the right bank of Stony Creek, nine miles above the township. It has a strike of 105°, and a northerly dip of about 45°. The outcrop has been proved for half a mile. The vein is from 3 ft. to 4 ft. wide, and consists of quartz seamed with mullock, and poor in gold. It carries frequent bunches of quartzose stibnite. At one spot a pocket of scheelite was found and extracted, and gypsum was found where the scheelite and stibnite were intermingled. This is no doubt a .secondary product, formed by the oxidation of sulphur and combination with the lime of the scheelite. The veins at Gabriel's Gully, near Lawrence; at Table Hill, near Milton ; and at Saddle Hill, near Dunedin, described by Ulrich in 1875, are now all closed down. (7.) The Barewood Claim. This is the best-known vein in the Taieri Gorge district, which includes several veins prospected at Hindon, Matarae, and elsewhere. The country rock is a quartz-mica-schist, lying almost horizontally. The vein strikes north-west and south-east, and dips north-east at an angle of about 60°. It is worked by an underlay shaft, which cuts the vein at a depth of 130 ft. At 180 ft. and 240 ft. crosscuts open up Nos. 2 and 3 levels, while a winze from No. 3 level has been sunk for a further distance of 30 ft. This is one of the few veins now being worked on the goldfield. It averages from 4 ft. to 5 ft. in width, but widens out to 15 ft. in the upper levels. It is composed of solid quartz throughout, divided by subordinate clay heads or partings parallel to the well-defined wails. The foot-wall is uninterrupted, but the hanging-wall carries small leaders (from 6 in. to 12 in. wide), which wedge out a short distance up. These leaders generally carry good gold. Fig. 4.- — Hangiisg-wall Leaders at Barewood. Slickensides are often well developed, generally on the hanging-wall. In places the quartz adjoining the walls, and also the adjacent wall-rock, are highly brecciated. This has been seen on both walls in No. 3 level, and on the hanging-wall in No. 1, while it is absent in No. 2. Horizontal Distribution of Gold. — The gold, so far as workings have disclosed, is uniformly distributed along the strike, and shows as yet no tendency to occur in localised shoots. FiNLAYSON. — Geology of Quartz Veins of Otago Goldfields. 77 Vertical Distribution of Gold. — The present depth of workings has disclosed an interesting variation in value from the No. 3 level winze to the surface. The accompanying section shows the values at different points, taking the average value through the whole cross-section of the vein : — /Y.yy. dufls. to ^3hcin 16 \ntermediateLz\el 1^ 10 20 /v'o. /. Le\.'&i till? V ^( ISO' No. ^. Level 1 80' No. 3 Level ^40' k <' 3 £. } Payable Ore.^ ^'^/ » 3otrreit Orz.- Fig. 5. — Cross-section of Barewood Vein. From the surface to a depth of 50 ft. the value rose from \ oz. to 1 oz. per ton. From here to the intermediate level the value fell to 16 dwt., and then more slowly, till at three stopes below No. 1 level it was 14 dwt. From here to No. 2 level the mean value became very low — approximately, 5 dwt. Between Nos. 2 and 3 there was an equally rapid rise, and at No. 3 it varies from \ oz. to over 1 oz. per ton, while at the foot of the winze the assay value is uniformly over 1 oz., and rich specimen-stone, particularly the brecciated variety, may be picked up showing much coarse gold. It is peculiar also that at this point the gold is often dark in colour and rusty. At No. 3 level, below it, and for some distance above it, the gold is pretty evenly distributed across the vein. Rising to No. 2 level, a barren block of glassy quartz comes in, and the seamy gold-bearing quartz is pushed over to the two walls, and divided by clay partings from the barren centre block, which corresponds practically to a " horse " of country rock. This block wedges out when followed in either direction along the strike, and it also has an easterly pitch or dip along the strike of the vein. Both these features may be seen on the accompanying plan of the workings. 78 Tronsactinns. where it will be observed that in each level the foot-wall and hanging- wall seams have been driven on, leaving the centre block intact. Shclfl Fig. 6.- W. -Mine-plan, Barewood. X Barren block. Thus in the wider portion of the vein the gold has been deposited in two shoots along the walls. The gold-bearing quartz differs from the barren " dog's-tooth " quartz in being seamed and mottled wdth pyritic mullock, and under the microscope is finer in grain. These facts point to a certain amount of replacement along the walls, while the barren block has been formed by simple deposition in an enlarged fissure. In places in Nos. 2 and 3 levels there occur pecuhar siliceous concretions (Plate II, 3), cavernous and irregular in form, with a fine chalcedonic banding. They are dark, and coated thickly with very fine pyrites. In appearance they suggest " clinkers " in coal, or fossil forms. Associated Minerals. — The dominant sulphide is pyrite, in fine crystals and grains. It is absent in the clear glassy quartz, and thickly distributed in the auriferous quartz. In the No. 3 level there was found within the vein, and near the hanging-wall, a narrow cavity containing a cluster of large stalactites of pyrite. Stibnite, galena, and scheelite occur occasionally. The only one of importance is stibnite, which is becoming common in the deeper levels. Habit of the Gold. — The gold is largely free, the assay value of pyrite being low. It is probable, however, that at a greater depth the ore will become refractory. FiNLAYSON. — Geology of Quartz Veins of Otago Goldfields. 79 Alteration of the Wall-rock. — The country rock is little altered, except for about 2 ft. from the vein-walls, where the alteration is considerable, the rock being soft and " muUocky." There is, further, frequently found on the walls a type of greasy yellowish rock, devoid of pyrite, and very similar to the corresponding rock described above in the Nugget and Cornish Mine. It accompanies the brecciated ore, the payable seams being well developed in No. 3 level and the winze. The following analyses indicate the alteration of the normal rock : — 1. 2. 3. 4. H20 1-68 2-11 1-58 — 0-10 SiO., . 62-02 65-30 48-97 — 13-05 AloOg .. . 11-15 14-70 11-15 , , Fe,03 .. 5-58 4-12 3-09 — 2-49 FeO 7-26 2-41 1-80 — 5-46 CaO 6-11 3-76 2-82 — 3-29 MgO 0-65 0-79 0-60 — 0-05 K,0 1-71 1-28 0-96 - 0-75 Na.,0 . . 3-34 2-05 1-54 — 1-80 Mnb 0-17 0-21 0-15 — 0-02 TiO. 1-01 0-37 0-27 — 0-74 FeS^ . 3-82 2-85 + 2-85 100-68 100-92 75-78 + 2-85 —27-75 1. Unaltered rock. 2. Altered rock. ^ -24-90 3. Altered rock, recalculated on a basis of constant alumina. 4. Gains and losses. The alteration in this case is more intense than at Skipper's, although more local, and the loss of material greater. It is, however, of a similar nature — namely, sericitic. Analyses made of the yellowish or bleached variety of wall-rock show that, like that at Skipper's, it is a kaolinized type of the ordinary sericitic rock, evidently formed by the action of descending waters. Ore-shoots of Primary Origin. — The characteristic hanging-wall and foot- wall seams described above doubtless originated during the primary de- position of the gold, through the influence of the wall-rock. Ore-shoots of Secondary Origin — Secondary Sulphide Enrichment. — A number of facts indicate that the No. 3 level winze has encountered a zone of enriched sulphides (pyrite and stibnite). These are as follows : (1.) The occurrence of the gold in the free state, and its frequent rusty colour. (2.) The occurrence of stalactites of pyrites. (3.) The peculiar siliceous concretions, probably due to solution and redeposition by subsequent leaching j)rocesses. (4.) The brecciation, signifying subsequent movement, would give readier access to descending solutions. (5.) The kaolinization and bleaching of the yellowish wall-rock, and the absence of pyrite in it, are evidently due to descending surface waters, and it is notable that it occurs associated with the brecciated ore and with the richest seams. (6.) Finally, the impoverish- ment in the upper levels, supported by the above data, points to the work of secondary enrichment, which has largely leached the gold out of the upper levels and redeposited it with sulphides in the zone now being opened 80 Transactions. up. It is probable that wlieu this zone is passed through the ore will become lower grade and refractory, as at Bendigo and ou the Carrick Range. (8.) Goffer -veins. There are two veins in the district carrying auriferous chalcopyrite — one at Moke Creek, near Queenstown, and one in Reedy Creek, near Waitahuna. I examined the outcrop of the Moke Creek vein, but little can be seen, and no information of importance was obtained. The ore is low grade, and the veins are small and of uncertain ore-content. Under the microscope there is seen to be a good deal of carbonate in the gangue (Plate II, 4), Ulrich described both these veins in 1875, and Rowe later described the Waitahuna vein (see Bibliography). (9.) Cinnabar -vein. One cinnabar-vein has been located— namelv, the Waitahuna vein, in a gully at the foot of the Waitahuna Hills, half-way between Berwick and Waipori. The vein is a small one, filled with pyritic mullock, which carries bunches and veins of very high-grade cinnabar. The mineral is highly crystalline in the frequent small cavities, the crystal form being prismatic with rhomb ohedral terminations (/•, 1011). Cinnabar is frequently found in the alluvial gravels throughout the Waipori district, and there is no doubt that there are other veins of this mineral in the neighbourhood. Such veins might escape detection owing to their small size, and to the soft and perishable nature of the vein- filling. The country is, moreover, unfavourable for the prospecting of such veins, being largely worn down into rolling foothills covered with tussock. A good deal of alluvial cinnabar has also been found in the Nevis and Nokomai district, and a vein doubtless exists there also, although none has yet been found. (10.) Fault- fractures and Barren Quartz Reefs. The occurrences described under this head have, as far as can be seen, no economic value. Fault - fractures. — The faults and crush-zones which extend through the goldfield are occasionally mineralised, and carry a few grains or more of gold to the ton. One of these occurs about three miles to the east of Bendigo, running about north-west and south-east.* In several places on the line of the fault prospecting-work has been carried on, and a little payable work done, but the irregular and very low-grade nature of the formation caused operations to be soon suspended. The workings disclose a belt of crushed schist traversed by small irregular veins of quartz. Green's reef, at Ophir, described by Ulricht and by Park,} is another instance of this type. Some years ago it gave a good return to its sole prospector. The occurrence of gold at Green's reef is cited by McKay as an instance of the occurrence of free gold in the schist.§ Ulrich has suggested that these " lode-formations " will, if developed, lead to a simple defined vein in depth. I i It is much more probable that * Park. Bull. No. 5. X.Z.G.S.. p. 56. t " Handbook of New Zealand Mines." 1887, p. 75. + Park. Bull. No. 2, N.Z.G.S., p. i'J. § McKay, '• Gold-deposits of New Zealand " (Wellington, 1903), p. 07. •-^ Ulrich, " Geology of Otago," 1875. |). 185. Trans. NX, Inst., Vol. XIJ. I'l.. II. Z634- QUARTZ VEINS OF OTAGO GOLDFIELDS.— Finlayson. F I— I X > H X Z n: ;?; X Z 05 ( 2 O z w O O) o o oi u < Z. o u CO < D Q Z < < o z o o < o > o o O Marshall. — Contact Rocks from West Nelson. 101 Art. XVIII. — Contact Rochs from West Nelson. By Dr. P. Marshall, M.A., D.Sc, F.G.S., University of Otago. [Bead before the Otago Institute, lOth November, 1908.] During a visit to Collingwood and West Wanganui, Mr. E. D. Isaacson recently collected certain rock-specimens which contain minerals formed by contact metamorphism, hitherto not recorded from New Zealand. All geologists who have visited this district have recognised the fact that large granite intrusions have been forced through older (probably Palaeozoic) sediments. The granitic masses of part of the district have lately been accurately mapped by Dr. Bell and his assistants, Messrs. Webb and Clarke. During the course of this work certain altered sedimentaries were encountered near the zone of contact, and in some of them andalusite was recognised. The specimens now referred to are as follows : — 1. Chiastolite Slate. Cleavage is highly imperfect. The chiastolite is not recognisable in hand- specimens. There are irregular grey spots ^ in. in diameter, which from their softness appear to consist of some secondary mineral. The section shows that the greater part of the rock consists of minute grains of quartz mingled with graphite-specks. The chiastolite crystals are as much as 0-15 mm. in diameter, and twice as much in length. They are perfectly fresh, and contain the characteristic inclusions of carbonaceous matter with a cruciform arrangement. Small crystals of staurolite are rather abundant, with the characteristic pleochroism and birefringence. The section contains much pyrite. The areas which appear grey in the hand-specimens become a pale-brown in section, with a high birefringence. They appear to be pinite pseudomorphs after cordierite. Other specimens of chiastolite slate are abundant as boulders in the gravels of the Aorere River, but sections show that the large crystals of chiastolite 100 mm. in length and 10 mm. broad have been completely changed to crowded plates of muscovite. 2. Cordierite Schist, Hand-specimen black, with distinct fractured black crystals. Section : The greater part of the rock consists of cordierite, perfectly clear and fresh, but crowded with minute inclusions of biotite and pyrite. Fluid-cavities are also common. None of the inclusions are surrounded with pleochroic halos. Some of the cordierite crystals are trillings, as shown in the figure. The crystals are 60 mm. long and 30 mm. wide. The rest of the rock consists chiefly of a reddish-brown biotite in irregular plates. Regular plates of muscovite are fairly common, and there is much pyrite. There is very little quartz. 102 Transactioi IS. Analysis. SiOa . . 59-08 Al.Og . . 17-60 Fe;03 . 4-17 FeO . 6-69 TiO, . 0-65 CaO . 0-70 MgO . 3-20 Na^O . 3-38 K,0 . 2-42 H^O . 2-40 " 100-29 It is probable that these rocks come from the metamorphic aureole surrounding the great granitic intrusion which extends from the west coast to the head-waters of the Aorere River, and from the Big River to the south of the Karamea. No doubt actual occurrences jn situ will be recorded when the geological survey of the area now in progress is completed. Fig- Fig. 3 EXPLANATION OF PLATE IV. 2. Mici'o. section of chiastolite slate from West Wanganui Inlet, West Nelson. A large chiastolite crj^stal is showii. with characteristic carbonaceous inclu- sions. The light part of the rest of the section is ciuartz, the darker portion is biotite. Magnified 25 diameters, ordinary light. Micro, section of a trilling of cordierite, showing numerous inclusions. Magnified 25 diameters, crossed nicols. Specimen from Aorere River, West Nelson. Art. XIX. — Crater of Ngauruhoe. By Dr. P. Marshall, M.A., D.Sc, F.G.S., University of Otago. [Read before the Otago Institute, \Oth November, 1908.] The earliest accounts of the crater of Ngauruhoe, by Bidwill and Dyson, show that considerable changes have taken place since these pioneers made the ascent of the cone. The former, in 1839, describes it as " the most awful abyss that I ever looked into or imagined." The stones thrown in did not strike the bottom in less than seven or eight seconds. It was im- possible to get into the inside of the crater, as the sides seen were, if not quite precipitous, actually. overhanging. Bidwill states that Ngauruhoe was in a state of activity at the time of his visit, and the steam prevented him from seeing more than 8 or 10 yards into the crater. This description applies perfectly to the crater at the present day if the volcano be more than usually active and the crater is reached on the south or east side. From other statements made by Bidwill it appears probable that he ascended the mountain on the north or west, and on those sides at the present time the crater-floor is almost level with the wall. It is reasonable, therefore, to suppose that the crater is now very different in form from what it was when Bidwill saw it. Mabshall. — Crater of Ngnuruhoe. 103 Dyson, in 1851, stood on the northern side of the crater. He says the lip was sharp, and inside there were large overhanging rocks of a pale- yellow colour. It was impossible to descend into the crater. This account corroborates Bidwill's statement, and emphasizes the fact that the crater had, in the middle of last century, steep walls all round — or, at any rate, on the northern side. Professor Thomas, in 1888, called attention to the form of the crater, and recorded that Mr. Jackson Palmer, then engaged in work near the mountain, had noticed that after a long spell of bad weather in 1888 a gap had been formed in the east side of the crater-wall. In 1887 Mr. Hill ascended the mountain, and at that time, and at a sub- sequent visit in 1892, the crater was in the same condition as it was in when I first saw it in 1891. Fig. 1, Plate V, gives an idea of its appearance. The small north-west-rim crater, called by Mr. Hill the " yellow crater,'" was then rather active, and steaming vigorously. The main crater had a floor nearly level throughout. We entered the crater on the western side. Near this side there was a violent escape of steam, though less in amount than that which escapes from Karapiti. Smaller steam-jets were issuing in many places, and most of them escaped from the summit of a cone of bright- yellow sulphur 2 ft. or so in height. The effect of all these small cones was very pleasing. It was possible at that time to walk all over the floor of the main crater, though the ground was hot and in some places soft. In 1893 the appearance of the crater had absolutely changed, though the small north-west crater still remained, but steamed much less than previously. All the small sulphur cones had disappeared, and near the centre of the main crater there was a deep black explosion-cavity. The explosion to which the formation of this was due had scattered mud and volcanic ash over the floor of the main crater, and had covered up the little sulphur cones. The explosion-cavity was then about 30 yards in diameter, and there was level ground between it and the north-west crater, and more between the cavity and western wall. In 1891 a report was published by Mr. Cussen on the Tongariro Mountains, and with it an excellent map : but it is stated in the text that though Ngauruhoe was twice ascended, the clouds of steam that issued from it prevented the surveyors from obtaining a clear view of the crater. It is, however, stated that the crater was circular, and the small crater on the north-west side is described. In the map another small crater is indicated, on the south side. This is probably an error, for no mention is made of it in the text, and it was certainly not there in January of that year. Dr. Benedict von Friedlander was the first to call attention in writing to the " hole " in the south-west of the crater. He visited the mountain in 1896, and was unable to see to the bottom of the " hole " because of the large amount of steam that issued from it. He does not state the extent to which the " hole " encroached upon the crater on the north-west rim. to which he, like all other observers, refers. In January, 1898, I was able to walk between the explosion-cavity, or hole " of Dr. Von Friedlander, and the small north-west crater, though the explosion-cavity was then much enlarged, and the level ground between it and the north-west cone was much reduced. The cavity had also extended considerably to the west, though there was still some level ground between it and the north-west crater. As in 1893, I was unable to see to the bottom of the cavity, because of the large body of steam that issued from it, though a long time was spent on its edge. The activity did not seem so pronounced 104 Tranmctioits. as in 1893, for in that year from time to time a rumble was heard in the interior of the mountain, and dense clouds of steam and dust were shot up. It is probable, however, that there was not much difference in this respect, for after returning to camp a rumble was distinctly heard, and soon after the dark cloud rose up from the crater. Another visit was paid in December, 1906, when the mountain was more than usually quiescent. It was found that the cavity had extended con- siderably towards the west, where now there was no flat ground between it and the exterior wall of the main crater. It had also extended towards the north-west crater, and had encroached on the small cone in which that crater was situated. During an interval when the steam lifted it was possible to see to the bottom of the cavity. It appeared to be nearly 200 ft. deep, with vertical walls on the east and north, but elsewhere bounded by steep walls, which on the west were a continuation of the wall of the main crater. The walls of the cavity were covered with jets of steam, and were encrusted with sulphur. At the bottom was a small lake of greenish-yellow water, on which masses of scum — probably sulphur — were floating, and there were specially strong steam-jets near the level of the water. At this time the crater certainly did not deserve the title of ■' bottomless pit," given to it a little later by a Press reporter. In February, 1907, the mountain became more active, and another visit was paid to it to find out whether the activity had caused any notice- able changes in the crater, and also to find out the exact nature of the violent explosions that occurred from time to time. A start was made early in the morning, when a dark cloud was rising 3,000 ft. above the crater. The appearance was then similar to that presented on the following morning, when the photograph was taken. When within 1 ,000 ft. of the summit it was found that the surface was covered with slimy mud to a depth of 1 in. The depth of mud increased as the summit was approached, when it attained a depth of 6 in. When 500 ft. from the siimmit the wind failed, and the black cloud rained mud on to the surface of the mountain. We were soon covered with mud from head to foot, but persevered in our ascent, though inky blackness enshrouded all the mountain-summit, and the air seemed filled with sulphur-dioxide. At the top it was impossible to see anything, nor were the sounds very different from those we heard on previous visits. Everything indicated that an explosive paroxysm had just ceased. The cold wind was so piercing that it was inadvisable to remain long at the top. We stayed as long as possible, but the air did not clear, and we had the satisfaction of seeing after our return that the black cloud still rested on the summit. The mud that fell on us had a strong acid character, for it bleached the colour from a print blouse that my wife was wearing. Pre- viously, in 1906, Mr. Flower, of Christ's College, Christchurch, had agreed with me that the smell of sulphur-dioxide was much more pronoimced than that of sulphuretted hydrogen, which goes to prove that the activity of the crater was at an unusually low ebb when Dr. Von Friedlander could detect the latter only during his visit in 1896. During this visit we were unable to see what changes had taken place in the crater, but it was evident from the foot of the cone that the exterior wall had suffered no changes. The gap in the eastern wall, to which attention was then called, was, as previously stated, formed in 1888. Although some overhanging crags at the side of the gap are in an extremely unstable state, and might be dislodged by the vibrations caused by a steam-explosion, no rocks have, so far as I know, fallen from it since the year 1891, when I saw it. Trans. N.Z. Ixst., Vol. XLI. Pl. V. Fig. I. Crater of Ngauiuhoe in i8gi. Fig. 2. The same in 1907. Face p. 101. CRATER OF NG AU RUHOE. — Marshall. Trans. N.Z. Inst., Vol. XLI. Pl. VI. CRATER OP^ NGAURUHOE. Marshall. Trans. N.Z, Inst., Vol. XL7. Pl. VII. CRATER OF NGA URU HOE.— Marshall. Marshall. — Additions io List of New Zealand Minerals. 105 The photographs taken by Mr. Browne at Easter, 1907, and by Mr. Cockayne this year, do not show any material change as a result of the rather violent activity that was in progress when the photograph (Plate VI) was taken. It appears, however, that the extension of the deep cavity westward and northward has been continued to a slight extent. In all my visits to the crater the escape of steam from it has been much more voluminous than is shown in the photograph of the crater taken by Mr. Cockayne.* There is one point about which I am not certain. A small mud-crater is to- be seen on the east side of the big explosion-cavity. When it was formed I do not know; it certainly was not there in 1891. It may have been formed at the same time that the explosion-cavity was blown out, though I have no note of its presence in 1893. To sum up : — 1. The form of the crater appears to have been very different in 1839 and 1852 from its present shape. 2. In 1891 the floor was level, except where the north-west crater was situated, which was then the most active spot. 3. In 1893 the north-west crater was less active, and the explosion- cavity was of small diameter near the middle of the crater, and was steaming vigorously. 4. Since that time the explosion-cavity has extended westwards and northwards, and the activity of the north-west crater has dwindled. 5. No escape of lava has occurred within historic times. 6. The main-crater walls have not changed since 1891. EXPLANATION OF PLATES V-VII. Plate V. Fig. L Crater of Ngauruhoe in 1891. Fig. 2. The same in 1907. Fig. 3. Tiie same in 1906. Plate VI. U])])er part of cone of Ngauruhoe, at 8 a.m., 14th Jilarfh, 1907. Photo taken from the .south-east ; distance, five miles. Pl.\te VI ^ Highest point of crater-wall of Ngauruhoe — the south-east side. Art. XX. — Additions to the List of New Zealand Minerals. By Dr. P. Marshall, M.A., D.Sc, F.C.S., University of Otago. \limd before the Oltijo Instiiute, Wlh Xorei/iber, 1908.] Ix the year 1890 Sir .lames Hector compiled a list of New Zealand minerals for inclusion in the " Transactions of the Australasian Association for the Advancement of Science " (vol. ii, 1890). Since that time a large number of papers have been written by a variety of authors on New Zealand geology. In these papers inauy references have been made to minerals that are not included in Sir James Hector's list. In the present paper these references "Tongariro National P.ak" : L. Cockayne. Parliamentary paper C.-ll, 1908. 106 Transactions. are collected together, and additions are made of other species and locali- ties known to the author but not hitherto mentioned in any publication. It is probable that the present list is still far from complete, but it will, at any rate, serve as an index to the various discoveries that have been made of late years, and may also be useful as a guide to those who may seek for general information as to the occurrence of mineral species in the Dominion. The arrangement followed is that adopted in Dana's " System of Mineralogy," 6th edition, 1906. SaLPHUR : Very good orthorhombic crystals at Rotokawa, near Lake Taupo. Zinc (3) : It appears somewhat doubtful whether this specimen was native or was produced by artificial means. Gold : No important new discoveries have been made. Crystalline gold has been recorded (8). Microscopic work has been done on some oc- currences at Ohinemuri (2). Silver (4) : In addition, flattened grains of alluvial silver have been found in some diggings in the Shotover River. Copper (9) : Crystallized copper of very recent deposition at Kawau Island. Lead (11) : The same occurrence as that mentioned in Hector's list. Platinum (18), (19) : The quantity of the mineral in these localities is small, and is of no economic value. Meteoric Iron : An analysis of the Wairarapa meteorite mentioned in Hector's list has been made by Mr. Donovan. Molybdenite : Large deposits in the Mount Radiant district, Karamea, in lodes traversing granite country. Orpiment (23), (31). Realgar (23), (31). Petzite (1). Argentite (23). Galena (23) occurs in some quantity in the Jupiter and Pluvius Mines, Te Aroha. Cinnabar (23) has been found at Waipori, Otago, but has not been mined successfully. Pyrrhotite (28). Large quantities at the Champion Mine, Nelson. Chalcopyrite : The new discovery at Mount Radiant appears to be im- portant. Pyrite : Good octahedral crystals are found in chlorite-schist at Parapara. Cubes are common in phyllite near Mount Aurum, Utago. Nagyagite (]). Kermesite (23), (31). Pyrargyrite is said to occur at Puhipuhi, near Whangarei ; also 32. Tetrahedrite (1). Kerargyrite (23) : Several pounds' weight, from Waikoromiko Valley. Cotunnite (1). Quartz : The quartz of the Waihi Mine is sometimes platy in structure. It is said to be pseudomorphous after barite. Precious Opal has been found in small quantity at Cabbage Bay. Hyalite : Incrustations are common on dolerite at Dunedin. Tridymite (7), (19), (26), (27) : Quite common, but in very minute aggre- gates, in the rhyolites of the volcanic region of the North Island. Senarmontite (6) : Common at Mount Radiant. Molybdite : Not uncommon at Mount Radiant. Arsenolite (23), (31). Marshall. — Additions to List of Neiv Zealand Minerals. 107 Corundum : A purplish-red variety, in crystals of moderate size, occurs with green niuscovite in boulders in the sluicing-gravels at Rimu, near Hokitika. Ilmenite : Typical crystals, but of microscopic size, occur in nepheline- basanite of the Domain crater, Auckland. PiCOTITE (16). Magnetite (15) : A chrome variety occurs in hartzbergite, Milford Sound. Small octahedrons are common in chlorite-schist, Otago. RuTiLE (16), (22). (28) : Microscopic crystals in granulites of south-west Otago ; also in schists, Otago. Pyrolusite (23). TuRGiTE (20) : Occurs with limonite at Parapara. GOTHITE (20). PsiLOMELANE : Small nodules in decomposed scoria, Seaview, Dunedin. Dolomite (32) : Pearl-spar, in the May Queen Mine, Thames. Magnesite (15) : A decomposition product of enstatite in hartzbergite at Milford Sound. Rhodocroisite (23). Arragonite : Pseudo-hexagonal crystals at Oamaru and Dunedin, in cavities in volcanic rocks. Cerussite (6) : Tui and Pluvius Mines, Te Aroha. Orthoclase : Crystals with Baveno development, though not twinned, occur porphyritically in the granite of Separation Point. The finer portion of the groundmass disintegrates readily, and the crystals form the sands and gravels of the beaches. The variety sanidine (5), (17), is common in alkaline rocks, Dunedin. MiCROCLlNE (22) : In many granites, notably at Golden Bay, Stewart Island ; Kahurangi Point and Dea's Cove, Thompson Sound. Albite, Oligoclase, ANDEf-ixE, Bytownite. and Anorthite : All of these species are mentioned in various petrographical papers as occurring in many rocks of igneous origin. No occurrences deserve any special mention. Anorthoclase (17) : Abundant in many alkaline rocks at Dunedin. Also at Campbell Island. Perthite (16), (17) : At Stewart Island and at Dunedin. Leucite : The locality mentioned by Hector in the list quoted was ap- parently an error. Microscopic crystals occur in a leucitophyre at Puketoraki, near Dunedin. Exstatite (15) : Very large crystals in a hartzbergite at Milford Sound; also mentioned by Hutton in North Island volcanic rocks ; occurs also at the North Cape, in a hartzbergite. Hypersthene (16), (19), (26), (27) : Hutton has mentioned the occurrence of this mineral at Lake Taupo, where crystals washed out of pumice form a })lack sand. Abundant in the volcanic region of the North Island, and in norites at Milford Sound, especially in the gravels of the Cleddau River and at the Bluff. Bronzite : This mineral has been referred to in geological reports on the Dun Mountain, but it appears that diallage was mistaken foi- it. Bastite (25) : Noted l^y Hutton in a rock at the Dun Mountain, where it is associated with diallage. Occurs also in a hartzbergite at the North Cape. 108 Tra?isactw?is. AuGiTE : Good crystals are obtained from weathered tufas at Otago Peninsula and Banks Peninsula. ^"Egibixe (5), (17) : Abundant in alkaline rocks at Dunedin. Also at Raro- tonga, but of microscopic size only. Hornblende : Many varieties have been recorded in different petrographical papers. The common green variety occurs widely in the diorites of the south-west Sounds (16) ; brown or basaltic hornblende at Dunedin and Banks Peninsula (5), (17) ; barkevicite (17) in alkaline rocks at Dunedin. RiEBECKiTE (30) : In granite boulders near Brunner, Westland ; also at Campbell Island. Arfvedsonite (29) : Small crystals in trachyte of the Cass Peak, Port Hills, Lyttelton. Tremolite : With garnet forming boulders in gravels at Lake Kanieri and other Westland localities. Actinolite (22) : Abundant in West Coast schists and in Otago. ^NiGMATiTE (Cossyritc) (17) : Quite abundant in phonolites and trachy- dolerites at Dunedin. Also at Campbell Island. lOLiTE : Abundant in some contact rocks near Aorere River, west Nelson. The form of crystal composed of trillings occurs in these rocks (P. Mar- shall, this vol., p. 101). Nephelite (5), (17), (19), (26) : Abundant in large crystals in tinguaites, basanites, and trachydolerites, Dunedin. Also in basanite at Auckland, and in tinguaite boulders at Brunner (30). SoDALiTE (17), (19) : Small crystals in phonolites and trachydolerites, Dunedin. Garnet (16), (18), (20), (21), (22) : Abundant in schist rocks, Otago and Westland. A somewhat remarkable form in Otago, where a rock occurs of a pink colour, containing a multitude of extremely minute crystals of almandine. Grossulaeite (24) : Occurs with diallage in a garnet gabbro of the Dun Mountain, Nelson. UvAROViTE (28) : Minute crystals at Dusky Sound. Chrysolite : Forms rock-masses of dunite at Milford Sound, as well as the other localities mentioned by Hector. Melilite (17) : Plates in basanite at Puketiraki, near Dunedin. Zircon : Abundant in a porphyry at Campbell Island. Andalusite (20) : Relatively large crystals in schists. Chiastolite : Found by Mr. Isaacson in the north-west of Nelson (P. Mar- shall, this vol., p. 101). Staurolite occurs with chiastolite (P. Marshall, this vol., p. 101). Sillimanite : With tourmaline in a specimen brought by Professor Black from Stewart Island ; also in minute needles in a mica-schist from Dusky Sound. ZoisiTE (18) : Occurs with epidote in schistose rocks in Westland. Epidote (17), (18) : Abundant in quartzite and schists, especially in West- land. Tourmaline (19) : Large crystals at Richmond Hill, Parapara, in chlorite- schist ; also in smaller groups of radiating crystals at the same locality. Analcite (17) : A rock-constituent, and in cavities in caraptonite, at Dun- edin. M-OSCOViTE : Large crystals in granite between George Sound and Lake Te Anau ; also widely distributed in minute flakes in schists in Otago and Westland. Marshall. — Additions to List of New Zealand Minerals. 109 BiOTiTE : A rock composed of large crystal plates at Port Pegasus, Stewart Island. FucHSiTE (28) : Also said to occur in Central Otago. Paragoxite : A green variety, in boulders in Jacob's Eiver, Westland. Phlogopite (21) : A mica between this and lepidolite, in the Alexandra area. Clinochlore : This is the variety of chlorite most commonly present in the Otago schists. Genthite (6). Serpentine (18) : Often mentioned, but no new localities deserving of special mention. BowENiTE (18), (15) : Excellent specimens have lately been obtained from Anita Bay, Milford Sound. At Teratama it is found with ordinary serpentine. Talc (18) : In schist, Westland, and at the Caples River, Lake Wakatipu. Glauconite : Common in Miocene sandstones and limestones throughout New Zealand. TiTANiTE : Granite of Separation Point, and common in granulites of the West Coast Sounds. MosANDRiTE : Minute crystals in trachyte at Perseverance Harbour, Campbell Island. Perofskite (17) : In diorite. Bell Hill, Dunedin ; also in a porphyry, Camp- bell Island. MoNAZiTE : Small quantities have been found in sands at Greymoutk Apatite : An earthy phosphorite, in limestones at Millburn, Otago. Pyromorphite (6). Hedyphane (23), (31). ViviANiTE (6) : Earthy form common ; also good crystals in moa-bones, Waitati. Barite : Tabular form at the Thames. Anglesite (6). Gypsum : Crystals at the Thames and at Oamaru. Epsomite (1) : Thames. Melanteeite (6) : Thames. Chalcanthite (6) : Thames. Alum : In the Hot Lakes District, at Waiotapu and Orakeikorako. Retinite : In brown coals tliroughout New Zealand. Bibliography. 1. 1891. Park,.!.: " Occurrence of Some Rare Minerals in New Zealand." Trans. Aust. Assoc. Adv. Sci., vol. iii, p. 150. 2. 1890. Haeusler, Dr. R. : " On the Microscopical Structure of the Ohine- rauri Gold." Trans. N.Z. Inst., vol. xxiii, p. 335. 3. 1891. Park, J. : '' Occurrence of Native Zinc at Hape Creek, Thames." Trans. N.Z. Inst., vol. xxiv, p. 386. 4. 1891. Park, J. : " Occurrence of Native Silver at Thames Goldfield." Trans. N.Z. Inst., vol. xxiv, p. 386. 5. 1891. ' Ulrich, G. H. F. : " The Occurrence of Nepheline-bearing Rocks at Dunedin, New Zealand." Trans. Aust. Assoc. Adv. Sci., vol. iii, p. 127. 6. 1892. Park, J. : " Occurrence of Rare Minerals in New Zealand." Trans. N.Z. Inst., vol. xxvi, p. 365. 110 Transactions. 7. 1892. Marshall, P. : " Tridymite-trachyte of Lyttelton." Trans. N.Z. Inst., vol. xxvi, p. .368. 8. 1898. McLaren, J. M. : " Occurrences of Crystalline Gold in the Coro- mandel Region." Trans. N.Z. Inst., vol. xxxi, p. 192. 9. 1899. Baker, W. H. : " Crystallized Native Copper on Mine-timber at Kawan Island." Trans. N.Z. Inst., vol. xxxiii, p. 336. 10. 1902. Park, J. : " Rock-phosphate Deposits of Clarendon." Trans. N.Z. Inst., vol. XXXV, p. 391. 11. 1903. Park, J. : " Native Lead at Parapara." Trans. N.Z. Inst., vol. XXXV, p. 103. 12. 1901. von Wolff, F. : " Liparit Lava von Mayor Island." Centralblatt fur Geologie und Mineralogie, p. 208. 13. 1905. Thomson, J. A. : " Gem Gravels at Kakanui." Trans. N.Z. Inst., vol. xxxviii, p. 117. 14. 1905. Andrew, A. R. :"" Clarendon Phosphates." Trans. N.Z. Inst., vol. xxxviii, p. 117. 15. 1901. Marshall, P. : " Magnesian Rocks of Milford Sound." Trans. N.Z. Inst., vol. xxxvii, p. 181. 16. 1906. Marshall, P. : " Geological Notes on >South-west Otago." Trans. N.Z. Inst., vol. xxxix, p. 496. 17. 1906. Marshall, P. : " Geology of Diinedin." Quart. Journ. Geol. Soc, vol. Ixii, pp. 381-424. 18. 1906. Bell, J. M., and Fraser, C. : '" Report on Hokitika Sheet, North Westland Quadrangle." Bulletin Geol. Surv., new series. No. 1. 19. 1907. Marshall, P. : " Distribution of the Igneous Rocks of New Zealand." Trans. Aust. Assoc. Adv. Sci., vol. xi, p. 4. 20. 1907. Bell, J. M., Webb, E. J., and Clarke, E. : " Report on Parapara Subdivision." Bulletin Geol. Surv., new series. No. 3. 21. 1906. Park, J. : " Report on Alexandra Subdivision." Bulletin Geol. Surv., No. 2. 22. 1907. Park, J. : " Cromwell Subdivision." Bulletin Geol. Surv., new series, No. 5. 23. 1907. Fraser, C. : " Coromandel Subdivision." Bulletin Geol. Surv., new series, No. 6. 24. 1907. Marshall, P. : " Note on the Gabbro of the Dun Mountain." Trans. N.Z. Inst., vol. xl, p. 320. 26. 1907. Marshall, P. : " Geology of the Centre and North of the North Island, New Zealand." Trans. N.Z. Inst., vol. xl, p. 80. 27. 1903. Sollas, W. J., and McKay : " Rocks of Cape Colville Peninsula." 2 vols. Govt. Printer, Wellington. 28. 1888. Park, J. : " Geological Survey Report on Dusky Sound." 29. 1907. Speight, R. : " Trachyte from Banks Peninsula." Trans. N.Z. Inst., vol. xl, p. 176. 30. 1907. Smath, J. P. : " Alkaline Rocks from Westland." Trans. N.Z. Inst., vol. xl, p. 123. 31. 1900. Maclaren, J. M. : "Geology of the Coromandel Goldfields." Pari, paper C.-9. 32. 1897. Park, J.: "Geology and Veins of the Hauraki Goldfields." N.Z. Inst, of Min. Eng., Auckland. Cotton. — Geology of Signal Hill, Duncdin. Ill Art. XXI. — Geology of Signal Hill, Dunedin. By C. A. Cotton, M.Sc. [Rend before the Otagn Institute, lOth November, 1908.] General Geology. The locks of Signal Hill, being all volcanic, contain no internal evidence of their geological age. They form, however, a part of the Dunedin group of volcanics, which are known to overlie unconforraably at Caversham and at Sea View a calcareous sandstone of the Oamaru system.* The Oaniaru system was placed by Captain Hutton in 1875 in the Lower Miocene, but in his later works he classed it as Oligocene.f Hector includes the Oamaru rocks in his Cretaceo-tertiary system ;t Park places them in the Miocene.§ The volcanic rocks are not in any case involved in the disturbances of the Oamaru rocks, nor have faults of any magnitude been observed in them. A considerable amount of elevation and depression has, however, since occurred, for the main valleys have been eroded far below the present base- level, and at Sandy Mount and elsewhere marine terraces are found at a considerable elevation. Most observers have supposed the first volcanic outbursts at least to have occurred during the same period in which the Caversham sandstone was deposited. Professor Park, however, taking into account the erosion of the Caversham sandstone, suggests the beginning of the Pliocene as the first period of volcanic activity. || There was either a prolonged period of volcanic activity, or there were two shorter periods separated by a period of quiescence, for conglomerate to a thickness of 100 ft., containing pebbles derived from the earlier volcanic rocks, lies in places upon the sedimentary rocks, and is covered by the later volcanic lavas. In places, also, fine shales with leaf-impressions occur above the sandstone and below the conglomerate. If, as suggested by Professor Park,|| these are of Pliocene age, the later eruptions which followed cannot be older than Pliocene. The occurrence of the conglomerate and the evidence of two periods of volcanic activity explains the unconformity between the earlier and later lavas of Signal Hill. Physiography. Signal Hill is a flat-topped elevation, extending as a ridge from Logan's Point in a north-easterly direction for a distance of three miles. The ridge then bends to the north and north-west, towards Mount Cargill. The greatest elevation of Signal Hill is 1, 21-1 ft. Less than half a mile to the * Marshall, " Geology of Dunedin," Quart. Journ. Geol. Soc, Ixii, 1906. t Hutton, " Geology of Otago," 1875; " Sketch of the Geology of New Zealand, ' Quart. .Joum. Geol. Soc. 1885; '" (Teological History of New Zealand," Trans. N.Z. Inst., 1899. X Hector, " Outline of New Zealand Geology," 1886. §Park, Trans. N.Z. Inst., 1904. II Park, ■' On the Geology of North Head, Waikouaiti," Trans. N.Z. Inst., 1903. 112 Transactions. south-east of the main peak is a steep rocky peak of about 1,000 ft. ; and to the south-west of the main peak are several smaller peaks, all, however, with gentle slopes. Three-quarters of a mile along the ridge to the north- east of the main peak is a small elevation known as McGregor's Hill. On the south and east the hill slopes down to the shallow waters of Otago Harbour, and at the south-western end to an enclosed bay known as Lake Logan. The gullies on the eastern and southern sides are of slight depth, and are occupied by small streams. A valley of considerable breadth and depth runs down to Lake Logan, and is occupied by the Opoho Stream, which rises in a swampy area near the summit of Signal Hill. On the north-west the ridge is bounded by the North-east Valley Stream. This stream always carries a considerable volume of water, and has eroded for itself a deep valley. The sequence of the rocks appears to indicate a great antiquity for this stream-valley. The stream has two branches, one of which rises on Mount Cargill, while the other has worked its head back in an easterly direction, and is cutting down the saddle to the north of McGregor's Hill. The upper part of this branch is still eroding its bed, but the lower part, and also the main stream, have reached base-level, and have filled the floor of the valley with alluvium. The North-east Valley Stream is fed by numerous small tributaries, the middle courses of which are generally through steep-sided gullies. Occurrence op the Rocks. The rocks of most widespread occurrence within the Signal Hill area are the phonolite of the Logan's Point type, the trachytoid phonolite of the Signal Hill type, and a basalt-flow which I describe as basalt No. 1. The basalt covers the top of Signal Hill, and extends across the upper part of the depression of the North-east Valley. The Logan's Point phonolite extends from near the summit of the hill to Logan's Point, forms a steep peak on the side of Signal Hill overlooking the harbour, and reaches to a point near Burke's. The Signal Hill phonolite has rather a wide occurrence about McGregor's Hill, and is found also in the North-east Valley. Besides these there is a distinct variety of nephelinitoid phonolite, occurring probably as an intrusion, on the saddle to the north of McGregor's Hill ; and there are several other basalts. The latter vary in composition from a very basic variety, occurring as a dyke on the Mam North Road, which appears to be the youngest rock described, to a variety approaching andesite, which appears to be the oldest rock exposed. The least basic of the basalts, which I have called No. 5, clearly underlies the Logan's Point phonolite at a point on the Main North Road a quarter of a mile from Normanby. In the valley below this point it is not to be found, being obscured by slips of phonolite from above. Between the phonolite and the underlying basalt in the section exposed there is a stream-deposit, with boulders derived from the basalt, proving an intermediate period of erosion. The Logan's Point trachytoid phonolite mass is of great thickness on the southern slope of Signal Hill, being continuous from below sea-level at Logan's Point to an elevation of 1,100 ft. near the summit. Towards the west, however, it thins out, until on the Main North Road there is a thickness of only 50 ft. between basalt No. 5 below and the main basalt- flow (No. 1) above. In the valley below, the Logan's Point phonolite gives place to the Signal Hill phonolite, but the junction is obscure. There is difficulty also in tracinif the boundarv between the two rocks on the eastern side. It is^ Trans. N.Z. Inst., Vol. XLI. Pl VIII. Geologfical Map OF SIGNAL HILL, DUNEDIN. N.Z. O /O 20 30 ■to ' ' ' t i ^)itBiK df ciiairu. Logan's Point W. BlffimsiE T %\i¥\ «ffl * #' : f! ' I i^_ : :. _ .. . ..± _ i^ ; _ . _.;- !:-_ _ : ^n- - .. . - ;... .:..i :. ..- :..:_ j V - -- --- ----- ------- it'vL :;:::::::::::::4;(:::^>vt:::":::::: ::::::::::::::::: :__ :::__: ii /:z jr ______ L i 2£=f — .----- - ^ ^^X- ^ O- - ._ . _ _jfe, £ ^ K : " " :. : : :. "li" xii^S, - :::":: V; /' -:::::;::::::::::::::::::::::-: 2^..^ -^ -- - ------ . - ^ ::::: : - - " : : .: _ : T* ._:: :: : . i_ : - ±:^^ :;: :.- ..:_. . . . ^& ?:5 ;: :; : ■" " " -"_ _:- -- ± ' /cr^Xi^- : ^ - - - - _ : : _ : :«;: :i;:il:;. :_ - ,_ . . _ . '■-j^ ' x;' ._ " n: --:4- .- - - _. _- - _. - -_i_- _L . 0 25 0?4. 022 O20 018 c 016 [ 014' 012 ^ 010 ^ 008 I 006 00^ 58 57 56 55 54 53 it 61 50 49 48 47 46 45 44 43 Fig. 2. 0 02 42 pt SiO; GEOLOGY OF SIGNAL HILL. Cotton. Trans. N.Z. Inst., Vol. XLI Pl. X. J fsf % ^ \ ^ a6 6G GEOLOGY OF SIGNAL HILL —Cotton. Trans. N.Z. Inst., Vol. XLI. Pl. XI. '^'4 K"-/. '^■m^ ~'^f ^j *«-^ t!^. "^^SS^Sftasi/ "';;i3Sii* l-i 2.67' 2, (") -«*^ •TUa ('') GEOLOGY OF SIGNAL HILL.— Cotton Cotton. — Geologij of Signal Hill, Dunedin. 113 however, practically certain, from sections exposed elsewhere — notably that at North Head, figured by Dr. Marshall* — that the oldest rock is the Logan's Point type, and that the Signal Hill type, which is closely related to the andesitic type of the North Head, rests upon it. The intervening basalt and basanite flows are not represented at Signal Hill, although a first inspection of the sections exposed along the Main North Road might lead to the belief that basalt intervenes between the flows of the two types of phonolite. Going up the road from Normanby one passes successively Logan's Point phonolite. basalt, and Signal Hill trachytoid phonolite. A closer inspection shows that, while the basalt overlies the Logan's Point rock, it also overlies the Signal Hill type, and is continuous with the main basalt- flow which covers the summit of the hill, and has the peculiar distribution to be described later. This mass of basalt evidently filled a depression which existed near the line of junction of the two types of phonolite, and which may have been the result of erosion, or perhaps was caused by the rapid solidification of the relatively acid phonolite lava. Section No. 1 gives the distribution of these rocks. In connection with both types of trachytoid phonolite it may be stated that, in places where the rocks are exposed in situ, the cleavage is approxi- mately horizontal. Above the phonolite of the Logan's Point type there occurs, on the Signal Hill Road, about the 800 ft. contour-line, a bed of scoria 30 ft. in thickness. From an undecomposed core in this a specimen of basalt was obtained of a much more acid type than the main basalt-flow which followed it. It is described as basalt No. 4. The main basalt-flow, described as basalt No. 1, covers the summit of the hill, and on the south-eastern side extends down only a short distance. It continues, however, much farther in a north-westerly direction, and to the north extends in a narrow belt across the head of the eastern arm of the North-east Valley towards Mount Cargill. This distribution is very peculiar, and it might be suggested that the basalt covering this area consists of a number of lava-flows, some of which alternate with flows of trachvtoid phonolite. This explanation, however, is not upheld by field evidence. The sections exposed on the Main North Road, and numbered con- secutively 1 to 10 on the accompanving map, are as follows : — (1.) Direction, N.E.-S.W. Height above sea-level, 330 ft. Basalt lies horizontally upon Logan's Point phonolite. (2.) Direction, N.W.-S.E. Height above sea-level. 480 ft. Basalt lies upon trachytoid plionolite (Signal Hill tvpe), dipping N.W. 12'. (3.) The section is not clear, but basalt appears to overlie Signal Hill phonolite nearly horizontally. Height above sea, 520 ft. (4.) Direction, N.W.-S.E. Height above sea-level, 550 ft. Basalt lies upon Signal Hill phonolite, dipping 12|° N.W. (5.) Direction. N.E.-S.W. Height above sea-level, 580 ft. Basalt lies upon Signal Hill phonolite, dipping 4i° N.E. The basalt is then con- tinuous for about half a mile. (6.) Direction, E.N.E.-W.S.W. Height above sea-level. 75<) ft. Basalt lies upon Signal Hill phonolite, dipping W.S.W. 8°. At (7) and (8) the sections are not clear, but between these points basalt is continuous. ♦Marshal), " Geology of Duiiedin," Quart. Joum. Geol. Soe, Ixii, 190f>. 114 Transactions. (9.) Direction, N.W.-S.E. Height above sea-level, 860 ft. Basalt over- lies Signal Hill phonolite horizontally. (10.) At Junction School. Heitrht, 920 ft. Basalt lies upon a convex surface of Signal Hill phonolite, dipping both N.W. and S.E. at an increasing angle. The diagrammatic section along AA shows the relations of the rocks. It is thus seen that the basalt-flow is everywhere later than the phonolite. Moreover, when all the above-mentioned basalt-outcrops are followed up they are found to be continuous with the flow covering the top of Signal Hill, and the flow is continuous across the deep valley to the north. At various levels, also, isolated patches of the same basalt occur on the spur- leading down to Opoho. It thus appears that the basalt flowed over a surface quite as uneven as the present surface of the hill, and filled up the depressions. That the basalt did not follow the phonolite in quick succession is proved by the occurrence of a considerable thickness of baked soil on the surface of the phonolite and below the basalt. No direct evidence of erosion, such as the occurrence of phonolite conglomerate beneath the basalt, has been ob- served, but it seems necessary to postulate a long period of erosion before the extrusion of the basalt which then filled up the depressions, and perhaps solidified on some of the slopes without filling up the valleys below. \i, however, the basalt be supposed to have flowed from Mount Cargill, the valley which then occupied the site of the present North-east Valley must have been filled to a depth of 1,000 ft. with basaltic lava. From the lower part of the valley the basalt, if ever it occurred there, has been completely removed by erosion. The ridges running down towards the North-east Valley are composed of basalt, while the gullies are eroded in the phonolite, which at the heads of the gullies is at a considerably higher level than the basalt at the lower parts of the ridges. This, together with the fact that the tongues of basalt occur in trough-like depressions in the phonolite, shows that the present ridges occupy the sites of ancient gullies. The basalt mass is made up of numerous successive flows. At many points there are interbedded layers of scoria, and also red bands, which appear to be baked surface clays. If this is correct, considerable intervals must have elapsed between the successive extrusions of basaltic lava. These beds or layers cannot, however, be correlated on account of their resem- blance to one another and of the similarity of the basalt of the diiJerent flows. The beds do not appear in any case to lie horizontally, nor to have a uniform dip and strike. The strip of basalt filling the upper part of the North-east Valley is surrounded by older rocks at a higher level on all sides except in the direc- tion of the mouth of the valley. Here the older rocks (phonolites) are at a lower level. Hence it appears that the ancient valley into which the basalt flowed had the same general direction as the North-east Valley. The ancient valley was nearly as deep as the present North-east Valley, and, if it be granted that there has been no subsequent tilting, had a gradient not quite so steep. A small area of basanite occurring on the Lower North Road scarcely comes into the area discussed. Its relation to the basalt is not apparent. It occurs at a considerably higher level than the neighbouring Signal Hill trachytoid phonolite, and so is considered younger than that rock. It is distant about half a mile from the clear sections on the Main North Road Cotton. — Geology of Signal Hill, Dunedin. 115 Several intrusions of both phonolitic and basaltic rock are found. The most striking of these occurs on the saddle north of McGregor's Hill. The rock, which is nephelinitoid phonolite, is not found in situ, but fragments are found on the surface over an area 40 yards by 150 yards, with its greatest elongation in the direction W.N.W.-E.S.E. Great variations occurring in the mineral characters of this rock in specimens collected within a few feet of each other, and its isolated occurrence, lead to the conclusion that it is intrusive. It is surrounded by a ring of basalt, an isolated remnant of the basalt-flow, which is here cut down by the action of streams approaching each other from opposite sides of the saddle. The intrusion, tlierefore, is later than all the lava-flows. A group of dykes of a very basic basalt occur on the Main North Road. One is vertical, and 5 ft. in thickness ; two others are irregularly inclined, and vary from 2 ft. to 3 ft. in thickness. Lower down the hill is a vertical dyke of the same character, 15 ft. in thickness. The strike of these dvkes is about east and west. In the upper part of the North-east Valley, about 500 yards south of the Junction School, there appears traversing the basalt a dyke of decom- posed rock. On account of its decomposed nature, no detailed examination has been made of tliis rocJc. It has a fine lamellar structure, developed to such an extent that the lamelhe may be pulled apart by the hand. Its colour is a creamy grey, and it shows numerous white crystals of feldspar not entirely decomposed. Some of these are very large, and some of medium size. Their occurrence gives the decomposed rock a micaceous sheen. On account of the abundance of feldspar crystals, the rock has been tentatively classed as a trachytoid phonolite. Sequence of the Rocks. From the above description the followinp' aopears to be the sequence : — 1. Basalt of an acid type. 2. Logan's Point phonolite. 3. Signal Hill trachytoid phonolite. 4. Eruptions of basaltic scoria of an intermediate type. 5. Main basalt-flows. 6. Dykes of extremely basic basalt. Intrusion of nephelinitoid phono- lite. Dyke of rock of doubtful composition, perhaps trachytoid phonolite. Source of the Lavas. Nothing definite can l)e stated as to the position of the vents from which the various lavas issued. In the case of the Logan's Point phonolite tlie greatest thickness of rock occurs in the southern portion of Signal Hill. On the western side it thins out, and to the north dips below younger rocks. In the precipitous peak on the south-eastern side of Signal Hill the cleavage-planes of the rock are highly inclined, while elsewhere they are horizontal. Possiblv this peak mav be the neck or plug which solidified in the ancient crater ; but the surround- ing rock does not show signs of having flowed from this point. Similar rocks also are described from Mount Cargill, from the opposite shore of Otago Harbour, and from Otago North Head, where a bedded flow occurs : but such a great thickness does not elsewhere occur as that in the main Signal Hill mass. Marshall, " Geology of Dunedin," Quart. Journ. Geol. See, Ixii. 190fi. 116 Transactions. The trachytoid phonolite of the Signal Hill type does not occur over so- great an area, nor, so far as is known, to so great a depth in the area described, but a similar rock has a wide occurrence to the north, as described by Dr. Marshall, and occurs also as a bedded flo^y at North Head. It may, then, be supposed to originate at some point north of Signal Hill. The acid basalt underlying the phonolites does not appear to have any close allies in the neighbourhood, although I have compared it with a large number of sections kindly lent for the purpose by Dr. Marshall. It cannot, therefore, be traced to its origin. The main basalt-flow closely resembles a basalt occurring as a neck on Mount Cargill. This may perhaps be its source. If so, the ancient valley intervening must have been filled to a great depth. The occurrence of the basalt at various levels on the inclined surface of the phonolites on Signal Hill is more easily explained on the assumption that basalt overflow occurred there, and the lava flowed down the slopes. It is difficult to draw conclusions as to the nature of the magmas from which the rocks were derived, but they are best explained by supposing the rocks to be derived from tw^o magmas, a basaltic and a phonolitic. The basalts became progressively more basic as vulca'nism died out. The interval between the first basaltic flow and the next must, however, as before stated, have been great. The phonolitic magma which supplied the lava of the Logan's Point type and the very much later nephelinitoid intrusion were similar in com- position, and probably identical. The Signal Hill phonolite is chrono- logically intermediate between these two, but not intermediate in composi- tion. It is much poorer in alkalies and richer in iron, and appears to be related to the trachydolerite of Mount Cargill.* It may have originated from a mixture of the basaltic and phonolitic magmas. No explanation based on the theory of magmatic differentiation i& applicable to the alternation of types, but the basalts, taken separately, may be conceived to be derived from a differentiating magma in its final stages. Petrography. Trachytoid Phonolite (Logan s Point Type). This rock is mentioned under the above name by Dr. Marshall. | At the typical locality (Logan's Point Quarry) the rock is distinctly trachytoid, and near the summit of Signal Hill even more so ; but in the south-east peak feldspar is almost absent, and the rock should be classed as nephe- linitoid. Macroscopic Characters. — In hand-specimens the rock is of a greenish- grey colour, flecked with green streaks. It cleaves readily into flakes. Microscopic Characters. — The structure is uniformly fine-grained in typical specimens, and holocrystalline. Flow structure is common wherever there is a considerable development of feldspar. In the typical rock from Logan's Point there are no phenocrysts. The chief constituent is ortho- clase or sanidine, but in some places feldspar becomes scarce. It occurs as bundles of fine needle-shaped crystals, some of which are of considerable * Marshall, " Geology of Dunedin," Quart. Journ. Gcol. See. Ixii, 1906. t Marshall, " Geology of Dunedin." Quart. Journ. Geol. Soc, Ixii, 1906. Cotton. — Geology of Signal Hill, Dunedin. 117 length — up to 0-5 mm. — but all are very narrow. Some show Carlsbad twinning. The crystals are often bent, and generally interwoven. The constituents next in importance are nepheline and a^girine-augite. The nepheline is not distinguished without staining, but in a stained section fully one-third of the rock is seen to consist of nepheline. chiefly in short hexagonal prisms, and partly as fine allotriomorphous grains. The maxi- mum size of the prisms is 0-1 mm. in length and breadth. Very small isotropic spots with low refractive index are put down as sodalite. The segirine-augite occurs as flakes and needles without definite crystal outlines at Logan's Point. Near the summit better - defined elongated crystals occur, which are also larger, being as much as 0-5 mm. in length. The maximum extinction-angle is 38°. The colour is bright green, and the pleochroism as follows : (a) grass- green ; (6) lighter green ; (c) apple-green. With this may be compared the pleochroism of pegirine from Laven, given by Rosenbusch :* (a) pure green to blue-green ; (t») olivine-green ; (c) yellowish grass-green. Associated with the segirine-augite are numerous minute crystals of deep-brown, almost opaque cossyrite, varying in size from minute grains or needles to crystals 0-1 mm. in thickness. The form of the crystals is rather indefinite, but as nearly as can be made out the prismatic angle is that of typical cossyrite (66°). The mineral exhibits a deep-brown pleo- chroism. The grains are scattered evenly throughout the rock, being often associated with crystals of the green segirine-augite. Magnetite is fairly abundant, in fine grains, while apatite occurs very rarely, in fine needles. No glass is present. The high percentage of both ferrous and ferric oxides may be noted as peculiar to the rocks of this district. Treatment of the finely ground powder with hydrochloric acid dissolves a considerable amount. This points to the presence of a large proportion of nepheline ; and the unusual amount of ferric iron obtained in solution by this method points perhaps to the solubility of cossyrite. Variations of the Logan's Point Phonolite. — On the peak above Burke's mossy aegirine-augite is very abundant, and phenocrysts also occur up to 0-3 mm. in length. Feldspar is very rare, and the rock should be classed as nephelinitoid. Cossyrite and magnetite are abundant. Near the top of Signal Hill the feldspar is relatively abundant, showing flow structure. At Normanby nepheline is abvmdant, as also is tegirine- augite, both as mossy growths and as phenocrysts of considerable size. These phenocrysts attain a length of 3 mm. or more, but are very narrow. They have sometimes a core of pinkish-grey augite. The extinction-angle of the segirine-augite is 36°, and of the augite 40°. Orthoclase needles are moderately abundant. Co3syrite and magnetite occur. The Logan's Point rock has been compared by Rosenbusch, in a pri\'ate letter to Dr. Marshall, with the apachite of Osann.t The chief resemblance, however, appears to be the presence of cossyrite. According to Rosen- busch,! ^^^ distinctiveness of the apachite type is stated by Osann to be the richness in the younger amphibole minerals, the microperthitic nature of the feldspars, and the presence of senigmatite. The last appears to be the only point of similarity. ♦Rosenbusch, Mikr. Phys., 1905. tT.M.P.M., 1896, XV, 394. t Mikr. Phys., vol. ii, p. 823. 118 Tranmctions. In chemical composition the Logan's Point rock is similar to a tinguaite from Edda Gyorgis, Abyssinia,* the analysis of which is quoted for com- parison : — Trachytoid Tinguaite, Phonolite,t Losn Phonolite, Edda Gyorgis Type, British Logan's Point. Abyssinia. East Africa. SiO. .. .. 57-00 57-81 58-37 Al.,03.. .. 16-06 18-74 16-65 Fe;03 ■ . . 5-53 5-76 4-09 FeO .. . . 3-22 0-42 3-03 MgO .. . . 0-64 Trace 0-37 CaO .. . . 1-51 1-28 1-66 Na.,0 . . . . 8-00 9-35 7-28 K,0 .. . . 6-18 4-52 5-46 H.,0 .. • .. 2-10 1-50 2-36 Tib., .. . . 0-39 , , 0-21 CI . . 0-45 The analysis is also quoted of a rock from British East Africa, called by Prior the Losuguta- type. J This rock contains cossyrite, and its ground- mass in particular appears closely to resemble the Logan's Point rock. Eocks with abundant cossyrite, which occurs in a manner analogous to its occurrence in the Logan's Point rock, are described by H. L Jensen from Queensland. § The Logan's Point phonolite was first described by Captain Hutton]j as an augite-andesite. ITe considered the groundmass to be chiefl}' glass, and mentions chlorite and a purple pleochroic augite. What he describes as chlorite is probably a>girine-augite, and the purple augite is not to be fotnid. He evidently also mistook the cossyrite for magnetite. Trachytoid Phonolite {Signal Hill Type). This rock has been so named by Dr. Marshall.^ It is certainly a trachy- toid phonolite, with only a sinall amount of nepheline. but it contains amphi- bole as its chief ferro-magnesian constituent. Corresponding to the large amount of ferro-magnesian minerals and iron-ores, the content of both ferric and ferrous oxides is unusually high, as shown by the chemical analysis, given later. The rock is tlius an exceptional one. Macroscopic Characters. — The colour is greyish-green, and the texture rather coarse. Numerous cleavage-faces of feldspar are to be seen, and also crystals of amphibole of vai'ious dimensions, some being as much as 1 cm. in length and breadth. Sometimes a horizontal platy structure is notice- able, but the weathering is often spheroidal, and isolated boulders have the appearance of basalt. Microscopic Characters. — The structure is porphyritic and holocrystalline, and the feldspars of the groundmass in places show flow structure. * Prior. Min. Mag., xii. p. 269, 1900. t Contains also IVInO, 0-43 ; P.,0.,. 0-08. + Prior, Min. I\Iag. xiii, 61, Feb., I!i03, p. 238, and plate v, fig. 2. § Jensen, " Geology of East Moreton and Wide Bay'Districts, Queensland," Proc. Linn. Soc. N.S.W., 1906,' pt. i. il Hutton, Proc. Royal Soc. N.S.W., 1889, p. 134. ^1 Marshall, " Geology of Dunedin."' Quart. Journ. Geol. Soc, Ixii, 1906. Cotton. — Geology of Signal Hill, Dunedin. 119 The largest phenocrysts arc feldspar of different varieties in slightly corroded crystals. Anorthoclase is common in large crystals. It shows fine lamellar twinning, crossed at right angles by another set of very fine and rather indefinite lamellae. As will be seen from the accompanying photograph (Plate X, fig. 2), these are too narrow and not regular enough to be attributed to pericline twinning of a feldspar of the albite-anorthite series. In thicker parts of the section extinction between crossed nicols is irregular. For these reasons this feldspar is regarded as anorthoclase. As sections parallel to the cleavage are not obtainable, the extinction- angle cannot be verified. Clear crystals of monoclinic feldspar with Carlsbad twinning are also common. They are referred to sanidine. Oligoclase phenocrysts are also common, with polysynthetic albite twinning. Sections perpendicular to 010, having equal extinction-angles measured from the twin line, on either side of it, extinguish at an angle of 5° from the twin line. Perthitic intergrowths are rather common. The feldspars all occur in broad prisms, up to 3 mm. or i mm. in length. Numerous phenocrysts of a deep-brown amphibole occur. They have definite crystal outlines when not entirely resorbed. Prisms and clino- pinacoids are developed, giving hexagonal cross-sections. The crystals are elongated parallel to the c axis. The optical characters observed are as \ -L , follows: a — a, b = b, c/\c= 15°. The axis c lies in the plane of symmetry. Pleochroism : {a) Pale yellovvash-brown ; (6) deep brown ; (c) deep brown. These characters show it to be intermediate between barkevikite and basaltic hornblende. The crystals are largely resorbed, being bordered, and in some cases entirely replaced, by fringes of magnetite grains associated with augite and a little calcite. This amphibole has evidently been one of the first minerals to crystallize, having probably an " intratelluric " origin. It has afterwards become unstable in the magma owing to altered conditions, perhaps of pressure. The feldspar needles surrounding the amphibole phenocrysts have a fluxional arrangement. An interesting comparison may be m.ade between this mineral and the amphibole of a somewhat similar rock described from tlie *' Beagle " collec- tion.* In that rock the amphibole is converted to tegirine-augite, and no mention is made of magnetite. This is considered to be the source of all the segirine-augite in the rock. The size of the amphibole phenocrysts in the Signal Hill rock varies from 0-3 mm. in length and breadth up to 1 cm. or more. Pyroxene phenocrysts are rare, and of small size. They are augite of a slightly sodic variety. The extinction-angle is 42°. The mineral is rather pale in colour, with very slight pleochroism, as follows : («) pale green ; (b) greyish, almost colourless ; (c) slightly yellowish-green. A few stout prisms of grey-coloured apatite occur, up to 0-2 mm. in length. Olivine occurs rarely, and is largely altered to serpentine. A glomero- porphyritic inclusion has been observed. In the centre is a large cross- * Geol. Mag., March, 1907, p. 100. 120 Transactions. section of grey augite, surrounded by a mass of allotriomorphic crystals of lime-soda feldspar and grains of magnetite. Groundmass. — The groundmass consists of lath-shaped feldspars, pale- green augite, numerous magnetite grains, and interstitial nepheline. The feldspar is chiefly orthoclase or sanidine, but oligoclase also occurs, with the same characters as in the phenocrysts. The feldspar laths vary in size up to 0*5 mm. in length and 005 mm. in breadth. The pale-green ;egirine-augite occurs in irregular crystals. It has the same characters as in the phenocrysts. The pleochroism is very slight. The maximum size of the crystals is 0-5 mm. by O'l inm. Nepheline does not appear without staining, but a stained section shows a moderate amount of interstitial nepheline. Associated with the nepheline is a little sodalite. There is no glass, and there is no cossyrite. The absence of the latter is rather remarkable, considering its abundance in the Logan's Point phonolite. Chemical Composition. — The proportions of ferric and ferrous oxides are both very high, corresponding to the large amounts of . ferro-magnesian minerals and magnetite present. The nepheline-syenite of Red Hill, New Hampshire, U.S.A.,* has a somewhat similar composition, excepting that its content of ferric oxide is much lower. An analysis of it is quoted for comparison : — SiO^ Al.O., Fe.,0. FeO MgO CaO NaaO K.O H,0 Ti(3., P.O. CI Order of Crystallisatio)!. — (1) Some (2) amphibole ; (3) feldspars (after this corrosion of the feldspars and re- sorption of the amphibole took place, with liberation of magnetite) ; (4) moi'e magnetite and pyroxene ; (5) feldspar of the groundmass ; (6) nepheline. Nephelinitoid Phonolite. Macroscopic Characters. — The rock varies in colour from lead-grey to green. It is dense, and fine-grained. Specks of dark pyroxene and large phenocrysts of feldspar, as much as ^ in. in breadth, occur. The green kind in particular has a platy structure. Microscopic Characters. — The structure is holocrystalline and porphyritic, the phenocrysts, however, being rare. The groundmass in some cases ap- pears cellular, and in other cases, where the nepheline is not so idiomorphic, there are alternate streaks of clear, fine-grained nepheline and mossy green a^girine. When phenocrysts occur they are large. Trachytoicl Nep heline -syenite. Phonolite, Red Hill, Signal Hill. New Hampshire. . . 54-15 59-01 . . 16-09 18-18 . . 7-35 1-63 . . 4-90 3-65 1-61 1-05 . . 3-86 2-40 . . 5-94 7-03 . . 4-41 5-34 . . 1-40 0-65 . . 0-41 0-81 . . 0-42 Trace . . 0-40 0-12 magnetite and all the apatite ; * Baylcy, B.G.S.A., iii, p. 250. Cotton. — Geolog// of Signal Hill, Duncdin. 121 Phenocrysts. — Large clear crystals of sanidine occur with Carlsbad twinning and cross-parting. In some cases they are elongated, and vary in length from 1 mm. or less to 1 cm. or more. Nepheline occurs in sharply idiomorphic short prisms, but only rarely. They are as much as 1 -5 mm. in breadth. Groundmass. — Feldspar is very rare. Orthoclase occurs rarely in fine needles, showing Carlsbad twinning. Nepheline is the chief constituent. It occurs abundantly in good idio- morphic crystals, in size about 0*06 mm., and also interstitially. It gives the section a honeycombed appearance. Associated with the nepheline is abundant mossy aegirine or opgirine- augite of a deep-green colour. It occurs in very small crystals without definite outlines. The extinction - angle measured from the direction of greatest elongation is in many cases low, although it is impossible to determine it accurately. The pleochroism is from green to yellowish-green. At least some of the mineral is, therefore, probably pegirine ; but a?girine- augite may also be present, though to a small extent. Magnetite grains are very rare. No glass is present, and no cossyrite. Order of Crystallisation. — (1) Magnetite ; (2) sanidine and nepheline phenocrysts ; (3) mossy pegirine and the nepheline of the groundmass. Chetnical Composition. — The analysis of a tinguaite from Alno, Sweden,* is quoted for comparison : — Nephelinitoid Tinguaite Phonolite, Alno, Signal Hill. Sweden. SiO., .. 53-80 50-26 Al,63 .. 18-72 20-15 Fe.,0, . . 4-99 3-67 FeO . . 3-59 2-62 MgO * . . 0-86 1-43 CaO . . 2-80 3-28 Na^O . . 8-82 8-09 KgO . . 5-20 4-67 H,0 . . 1-90 3-85 TiO., . . 0-30 0-24 CI . . 0-14 Basalt No. : I. Numerous flows of this rock occur, making up the chief basalt mass. All are very similar. Only one, which differs somewhat in texture, is briefly noticed separately as basalt No. 2. Macroscopic Characters. — The rock is black and basaltic-looking, with numerous crystals of olivine and feldspar. No true columnar structure is to be seen, but some weathered boulders have the appearance of square prisms. Spheroidal weathering is general, and everywhere the solid rock is covered by a mantle of clay with spheroidal cores. Microscopic Characters. — The structure is holocrystalline and porphyritic. Large phenocrysts of feldspar, augite, and olivine occur in a groundmass * Rosenbusch, Elemente. p. 215, 1898. 1-22 Transactions. consisting of feldspar, magnetite, and augite, without glass. Flow structure is apparent in some localities and absent in others. Phenocrysts. — Phigioclase phenocrvsts vary in size up to 1-5 mm., and are abundant. Polysynthetic albite twinning is universal. The extinction- angle of adjacent lamelLnp in sections perpendicular to 010 is 30°. The feld- spar is therefore labradorite. Augite phenocrvsts are large, being as much as 7 mm. or 8 mm. in length and 2-8 mm. in thickness. The colour is grey, and the maximum extinction- angle 41°. The crystals are idiomorphic, and some show twinning, with the orthopinacoid as composition plane. Magnetite occurs in crystals and rounded grains up to 04 mm. in dia- meter. Olivine occurs in rounded crystals up to 0-5 mm., and, more rarely, larger. It is pale in colour. The olivine crystals are often replaced by serpentine pseudomorphs. Groundmass. — The groundmass consists chiefly of irregularly arranged small needles and laths of labradorite and numerous irregular grains of grey augite and magnetite. At some places feldspar is very abundant, with flow structure, and at others no flow structure is to be seen, while magnetite and augite are relatively more abundant. Chemical Composition. — For comparison the analysis of a dolerite* from Dyer's Pass, Canterbury, is quoted : — SiOg AL,03 Fe,03 FeO MgO CaO Na,0 K.b H^O Tib 2 CI. Basalt No. 1. Doleiite. Dyers Signal Hill. Pass, Canterbury . ■15-80 48-60 . 17-91 17-87 6-U 6-20 8-69 5-76 3-92t 4-32 8-10 9-11 4-71 4-66 1-77 2-06 2-10 1-78 0-35 , , 0-11 , , Bamlt No. 2. This basalt is not found in situ, but only as spheroidal cores in a deep clay. It has a cubical fracture. The minerals are similar to those in No. 1. and occur in the same proportions. The groundmass is similar to that of No. 1, the only difference being in the phenocrysts. The feldspar pheno- crysts are much larger than in No. 1, and the olivine is nearly all decom- posed. Basalt No. 3. This rock, which occurs in a dyke, is very hard and dense in appearance. Olivine crystals are seen in abundance. Microscopic Characters. — In sections the rock is holocrystalline and porphyritic. The groundmass is much more coarsely crystalline than that of the lava basalts. * R. Speight, Trans. N.Z. Inst., vol. xxvi, p. 409. f MgO appears low to be associated with such a low amouiit of SiOo- CoTTOi^. ^Geology of Signal Hill, Dunedin. 123 Phenocrysts. — The phenocrysts are augite, olivine, feldspar, and magne- tite. Of these, olivine and augite are by far the most abundant. The olivine crystals are large, and are partly altered to serpentine. They are almost colourless. The augite crystals are grey in colour and up to J mm. in breadth. Thev have no pleochroism, and the extinction-angle is 41°. Feldspar phenocrysts are rare. They are of basic labradorite, chiefly untwinned, and are about 1 ram. in length. Magnetite grains occur up to 0-1 mm. in diameter. Groundmass. — The groundmass is holocrystalline, and is coarser-grained than in the other basalts .described. It consists chiefly of allotrimorphous grey augite, with labradorite laths averaging 0-3 mm. in length. The extinction-angle on either side of the albite twin line in sections perpen- dicular to 010 is 32^°. There are also abundant grains of magnetite. No glass is present. This rock, owing to the scarcity of feldspar and abundance of augite and olivine, approaches a magma basalt or augitite. Chemical Composition. — The chemical composition proves that the rock is derived from an extremely basic magma. For comparison the analysis of a basic basalt from Punta Delgrada, San Miguel, Azores,* is quoted : — Dyke Basalt, Basalt, Punta Del- No. 3, grada, S. Miguel, Signal Hill. SiO, AUO3 Fe,03 FeO MgO CaO Na^O KoO H.,0 Tib., PoO, CI MnO .. .. .. .. .. 0-36 Signal Hill. Azores -44-00 44-06 14-07 15-10 5-16 5-23 10-87 7-93 11-18 9-84 10-28 12-56 1-74 2-20 1-98 0-93 1-40 0-30 0-47 1-80 0-53 0-11 Basalt No. 4. This basalt occurs in fragments in a scoria- bed on the Signal Hill Road, lying above the Logan's Point phonolite and below the main basalt- flow. Macroscopic Characters. — The structure is porphyritic. the matrix being grey and fine-grained, with numerous white phenocrysts of feldspar and occasional black specks of augite. Microscopic Characters. — In sections the porphyritic structure is strongly marked, augite and feldspar occurring in two generations. No flow structure is discernible. *€. V, John, Jb. G. R.-A., Wien, xlii, p. 291, 1896. 124 Transactionf/if of Signal Hill, Dunedin. The chemical classification is as follows : — 125 C ffi ^ :K c; n" ? * ~ Oj i:; ^ -"< f! S cS 33 Q CC (M C-l — -X — ' --C — ' Hit . -O t^ o — -— ^ -^ ~ £ -^ 4 ir: 1^ -^ « I- d c • • ^ ^ j: :: -^ 1 __ d 1 as 3 fi^=^ o . © CD 2^ ^ m C E-i ^ ^ S 5 X Q _© ^ o Q ^ ^, ^, ;S I— ' ^ 'v< -h" bjD j: c; Ml ^■ '^^ 3 ^ P5 X a ■^ — -t ~. I^ '^ (M — '3 6 . iC 3; C-l t- i: -+ X --c £ 6 3: c^3 i 4" i: X 6 • • t. — 1 ^ ^M — — . . O 1^ ._ _: _ -^ ce C3 « • ~-s a; 1. ^ . a< 4) oo M o S -,. ^ c O o X — -M -t r^ il&ll X" . 1- c -f 1- -M -f - - o ° ^ 5 ro r-H -^ , . nitoid 1 P c '^l 4 >r: — -t i • • • -~ re "^i ■M — ... P. O r. = - ^ = — S — o ^ ~ - P^x oj ai oj oT !!> tj K a: o i ^ :e O ^ s :: S ^ Ji! — C -r S 3j ® £5 C ■--: TC -f X -x — t- :c ^ c5 ^ ^ -^ -*- . QC — t;- X X — . C^ -^ t;- O -^ X C C- ^ ■^ , ^^ -J i_j .'>ICC ' ''^-"^^"^ 'O'S ll" 5 * M - "Z -.^ c '^ z ■--$__ ^ S ^ '-': - 4 CKTti-r. ^rsr^ce ^|SSP=: 2 ^. 14" "H s -= H ^ C a: -^ (D aT ■ S 3 It O -^ "S ^ — " £&- i, :2 ^ S "^ ■«-2 ^ CC "M ^^ ^ '■+^ , ' — ^ ^ ■^1 o •§3 "--■^-"~ = =" C3 H The " norm " is seen to correspond roughly to the " mode," or actual mineral composition. It is interesting to compare the actual proportions of feldspar to feld- spathoid in the three types of phonolite : (1) In the Logan's Point phonolite, where feldspar and nepheline each constitute about one-third of the rock, silica is relatively high and alumina low, while alkalies are high ; (2) in the nephelinitoid phonolite, where nepheline constitutes the greater portion of the rock, silica is lower, alumina is higher, and alkalies are about the same ; 126 Transaction.?. (3) in the Signal Hill plionolite, where neplieline is rare and feldspar of various tvpes abundant, silica is nearly the same as in the nephelinitoid type, alumina is low, and alkalies are also low\ EXPLANATION OF PLATES VIII-XL Plate VIII. Geological map of Signal Hill, with sections along lines AA, BB, CC, on map. Plate IX. Fig. 1. Map showing locality. Fig. 2. Graphic representation of the chemical composition of the rocks (after Iddings). Plate X. Fig. 1. Logan's Point phonolite ; x 200. Shows association of cossyrite and aegirine- aiigite. Fig. 2. Signal Hill trachytoid phonolite ; x 45. Crossed nicols. Shows large crystal of anorthoclase. Fig. 3. Signal Hill trachytoid phonolite ; x 45. Shows a large crystal of amphibole partly resorbed. Fig. 4. Nephelinitoid phonolite ; x 45. Shows the groundmass consisting chielly of nepheline with mossy aegirine. Plate XI. Fig. a. Logan"s Point phonolite overlying basalt No. 5 on Main North Road, near Normanby. Fig. b. Dyke of basalt No. 3, intruded in basalt No. L Art. XXII. — Further Notes on New Zealand Starfishes. By H. Farquhar. Communicated by H. B. Kirk, Professor of Biology, Victoria College. [Bead before the Wellington Philosophical Society, ItJi October. 1908.] Stegnaster inflatus, Hutton. Plate XII. This species has not been figured before : the figure now given is from an example found at Island Bay by Mr. Stuckey, headmaster of the Island Bay State School, and photographed by Mr. A. Hamilton, in which R = 63 mm., and r = 52 mm. The species is interesting as being the type of Sladen's genus Stegnaster. In his monograph Sladen says, " I have also added in the following list another genus, Stegnaster (n. gen.), which seems to me necessary. The type of Stegnaster is the starfish described by Hutton under the name Pteraster inflatus, and subsequently placed under Palmipes by Perrier. I consider that the disposition of the papuhe, the membraneous investment of the abactinal area (with the absence of the characteristic tufts of spines and the presence of granules), and the simple character of the armature- of the adambulacral plates, are sufficient to warrant the generic separation of this form from Pahnipes. I also refer to the same genus Asterina ivessli, though not without some hesitation, as the examples I have seen of that species appear to be immature forms."* * " Challenger " Reports, vol. xxx, p. 375. Farquhar. — Further Notes on Netv Zealand Starfishes. 127 I have not been able to discover that the association of A. wessh', a West Indian species, with Ste. (iS et seq. Smith. — Captain D'Urvilles Visit to Tologa Bay. 131 After attempting to laud, but prevented ])y the surf, the corvette proceeded along the east coast past Cape Palliser, the name of which (Kawakawa) is correctly given as furnished by the two Maoris, and on the 1st February they were oft' Cape Topolopolo [Te Poroporo], the Cape Turnagain of Cook. " At lOh. 10m. on the 3rd February we rapidly passed at half a league's distance L'ile Sterile of Cook [Bare Island], of which the true name is Motou-Okoura [Motu-o-Kura]. It is an escarped rock, naked, and a mile or more from the land. A pa (or fortress) of some size occupies the summit, and ought to be an impi'egnable position. There were also to be seen several houses on the slopes of the isle, and by aid of the glass we easily distinguished the inhabitants moving about their fortress, and occupied in regarding attentively our passing. As at other points of the coast, they had made some great fires to call our attention.. A cano6, well armed, came from Motou-Okoura to meet us. It was reported to me that our two Natives had uttered cries of joy on seeing it, and, charmed to be able to offer them the means of escaping from their captivity, I laid to. Already the canoe was but a cable-length from the side, when I announced to them that they were at liberty to seize the occasion to go ashore. What was my surprise to see both, at that proposition, become desolate, cover their faces, and roll on the deck, with all the signs of despair, declaring with energy that they desired positively to remain on board. They then informed me that the people of Motou-Okoura were their enemies, and that if they fell into their power they would be put to death and devoured. They invited us in the most unequivocal manner to fire on and kill them. The late transports of joy of our guests were only proofs, as I soon learnt, of their persuasion that we should exterminate the new-comers, and of their hope of a repast, which, according to their ideas, would become the prize of victory." After passing Cape Mata-mawi [Matau-a-Maui — Cape Kidnappers of Cook] the corvette sailed some six or seven miles into Hawkes Bay. Re- ferring to Scinde Island, on which is now built part of the town of Napier, and the adjacent country, D'Urville says, " We believed we saw an island of some extent situated close to the coast, which escaped the researches of Cook, but which may well be only a peninsula. There is reason to presume that between it and the mainland there may be good anchorages. In the south-west of Hawkey Bay we were able to see a pleasant landscape, dotted with clumps of trees, and on the edges some large basins of calm water, but which prol)al)ly do not oft'er sufficient depth of water for anchorages. [These no doubt were parts of Te Whanga-nui-a-Rotu (Napier Harbour) and the lagoons near Clive.] From three or four plains disposed in amphi- theatres the ground gradually rises up to the high moimtains of the in- terior ; and in all New Zealand that part is witliout doubt the richest and most attractive that has been offered to my gaze. This country seems well peopled, as denoted by the numerous columns of smoke arising from many points." [This is the country about Hastings, Clive, Havelock, &c., one of the finest in the Dominion, then inhal)ited Ijy the powerful Ngati- Kahu-ngungu Tribe.] After passing Portland Island, off the Mahia Peninsula (which D'Urville calls Tera-Kako. after Cook, but the origin of which is not known), on the 4th February the corvette was off Poverty Bay. Here we shall follow the narrative of the voyage lit rally : — [On the 4th February, 1827] we doubled at 2 p.m. the Cape Young Nicks, memorable for having been the first point of New Zealand seen by the 13"2 Transactions. illustrious Cook ; we passed quickly the opening of the Bay Taone-Roa [? Te One-roa — Poverty Bay], the lands at the bottom of which we could only distinguish indistinctly. At 4 p.m., in 35 fathoms, we made a stoppage at about 4 leagues from Cape Gable [Gable-end Foreland — Pari-nui-te-ra]. We know that this name was given by Cook because of its resemblance to the wall of a house comprised betw^een the two roofs. . . . The coast, which had retained a wild aspect from the Isle Tea-Houra [Portland Island] up to the S.W. point of Taone-Roa [Poverty Bay], beyond that assumed a less severe appearance. The surroundings of Cape Gable are particularly agreeable, and there are sites where culture would make fertile fields. There the columns of smoke again showed in greater number than elsewhere, proof infallible of a more numerous population. Towards 6 p.m. we approached the Tologa Bay of Cook, and I counted on doubling it before night, when the breeze, which had already decreased, fell entirely, and the corvette remained immovable at three or four miles from the coast. At 7 p.m. we thought we saw a small schooner, which at first ran along the coast, and then all of a sudden put out to sea and dis- appeared— a manoeuvre which I could only account for by supposing that the craft viewed our visit as not quite an agreeable one. At 8 p.m. two canoes, which we had observed for some time paddling towards us, came alongside without any fear, and as though accustomed to see Europeans. They sold us some pigs, potatoes, and other objects of curiosity in exchange for hatchets, knives, and other trifles. Forty -five days had passed since our departure from New Holland, and all our fresh provisions had been exhausted long since. It may therefore be judged with what pleasure these articles were received, above all when they told us that pigs were plentiful at Tologa, and that they would sell them at the lowest price. Te Rangui-Wai-Hetouma, chief of the New-Zealanders who came to visit us, announced himself as one of the principal rangatiras of the district, and wished to send his canoes ashore tO' procure pigs and potatoes, and to pass the night with us. I was well satisfied with this proof of confidence in us, but, fearing for him the same troubles (sea-sickness) as those of Tera-Witi. I refused, and obliged him, much to his regret, to re-embark in his canoe. I promised, however, that he would find us in the same place in the morning. Tehi-Noui and Koki-Hore appeared now to have regained their spirits, for a copious feed of dolphin-flesh, and the prospect of another next morning, had quite enchanted them, and in the evening a shark that had been caught completed their delight. Overcome by this abundance, they seemed little disposed to acquiesce in the desire I expressed to leave them here. Koki-Hore particularly did not relish that proposition. All night there was only a feeble breeze from the west, with superb weather. At 10 p.m. we laid to in 53 fathoms, muddy sand. 5th February. — In the morning, the breeze having changed to the N.N.W., which did not permit us to continue along the coast. I decided to profit by it to make a stoppage at Tologa. At 7.30 a.m. we steered for the bay, and at 11 a.m. the " Astrolabe " dropped her anchor precisely on the same spot where the " Endeavour " had anchored fifty-five years before. The Natives came out to us at an early hour, but I did not permit many on board. Arrived at the anchorage, we were soon surrounded by canoes full of islanders, who came to traffic with the crew. However turbulent and noisy in their bargaining, they showed much good faith, and we could only felicitate ourselves on the nature of our exchanges. The usual price for a fat pig was a large hatchet ; a small one would j^urchase a young pig. Smith. — Captain D^hville's Visit to Tologa Bay. 133 For indifferent knives, fish-hooks, or other trifles we obtained potatoes in profusion. It may be judged what an ample supply of fresh provisions we obtained for the crew and our tables. I at once sent MM. Jacquinot and Lottin to the watering-place of Cook to observe the latitude and longitude. At 1 p.m. M. Paris departed to sound the channel. The naturalists and the artist also went ashore to follow their avocations. I remained on board with the other officers to watch the movements of the Natives — a precaution which I judged more necessary here than elsewhere, as much on account of their numbers as their physical force and turbulent disposition. Already I had nearly drawn upon myself the animosity of one of these redoubtable savages — a thing I was anxious to avoid at any price, above all on account of those persons the nature of whose work obliged them to go ashore. Thus, as I have already said, whilst we were under sail I had kept off all the canoes which approached the ship, and only allowed Wai- Hetouma, who said he was chief rangatira of the place, to come on board with another Native whom he had represented as one of his near relatives. It is well to remark that this chief, who appeared to have received all his insignia, to judge by the complete tattooing of his face, was a peaceable man, easy and honest, and that he had applauded my resolution not to let any one on board beyond himself and companion. Most of those who presented themselves obe}'ed the prohibition against them, although with visible repugnance ; but one amongst th m would not obey the sentinel, and only left when trembling with rage at the peremptory order I gave him myself. It was plain to see that from his canoe he menaced me. By his stature and haughty mien, and the air of submission of those who sur- rounded him, it was obvious he was a chief. Moreover, a young woman in his canoe who spoke a mixture of English corrupted and New Zealand did not cease to repeat to me, with an extraordinary volubility, that Shaki,* her master, was a great chief and friend of the English, and that it was very bad of me not to receive him. Of course, I could afford to mock at these menaces against myself ; but I have explained the motives which guided me in dealing with these savages, especially the chiefs. Therefore I called Wai-Hetouma, and asked him who was this new-comer, so urgent. He allowed that Shaki was a great chief, and soon I had reason to believe he was superior to AVai-Hetouma in rank, or at least in influence. I then made a sign to Shaki to come on board, and explained amicably to him that I was unaware he was a distinguished rangatira, and gave him a few presents, which soon effected a change in his demeanour. From that moment we became the best friends in the world, and he was one of the last to quit the corvette^ from which he never budged an instant whilst we were there. This Native, who seemed hardly thirty years of age, was at least 5 ft. 9 in. high ; his form was athletic, with a martial air. He told me he had seen many English, and had been the companion-in-arms of Pomare, of Mata-ouwi [Matauri — Bay of Islands], that celebrated conqueror of New Zealand. The name of Shongui-Ika [Hongi-hika] was also known to him, luit he said he had never seen him. [Pomare, here referred to, was the celebrated Nga-Puhi chief of that name, who made several warlike ex- peditions down the East Coast, the principal one in 1823, when possibly Shaki joined him.. Pomare was killed on the Waipa River in 1826.] * We borrow from the English the form sh to represent here and in the course of this work a sound intermediate in some sort between that of / and ch in French. 134 Traiisacfions. In spite of my precautions, it was plain how very nearly I had made an implacable enemy of Shaki. On returning ashore he might perhaps have avenged on the officers or the naturalists of the " Astrolabe " what he considered an affront offered to his dignity. This is what often occurs to Europeans, especially among a people so irritable, so vindic- tive, as those of New Zealand, where the chiefs are all independent, and very jealous of one another. This latter sentiment, which renders the posi- tion of Europeans so very uncertain, is carried beyond bounds among the Natives ; they all want to profit exclusively in the advantages due to the visits of strangers, and are jealous at seeing their neighbours participate in them. We had a very extraordinary proof during our stay at Houa- Houa [this is the nearest D'Urville gets to Uawa, the proper name of Tolosa Bay]. Whenever fresh canoes arrived, the first-comers harassed me with re- quests to fire on them, and kill those on board ; nevertheless, so soon as the latter came alongside, the first-comers immediately entered into con- versation with them, and received them as persons well known to them. . . . . I could not refrain from laughing at this singular behaviour, when all of a sudden a general movement, a sort of confused murmur, arose amongst the Natives ; they cast unquiet glances overboard, and soon I saw the trouble was occasioned by the arrival of a canoe manned by seven or eight men only, among whom two seemed of superior rank. This time our guests prayed and supplicated me earnestly to shoot the new-comers ; they went so far as to demand muskets to shoot them themselves — in a word, they employed all possible means to excite my anger against these strangers. Far from acceding to these sanguinary wishes, I felt more inclined to receive amicably those who were in such repute, and to assure them that they would be well received. They appeared to hesitate for some time, and, together with the evident desire to come on board, a shade of inquietude and suspicion was apparent. In the meantime the conduct of the other islanders towards them totally changed. Convinced that I would not concede to their prayers, they assumed a very respectful manner towards the new-comers. Shaki himself, until now so bold and most urgent that I should fire on them, changed his tone suddenly ; he became modest and silent, and so respectful to the two strangers that he offered them some large hatchets which he had only acquired with much trouble, and to which he seemed to attach as much value as to .his life. This procedure was followed by all those who had not had time to hide what the}^ had received from us. The two chiefs finally decided to come on board. I examined attentively their completely tattooed faces and their warlike and fierce attitude. I have never observed these double qualities so pronounced in any New- Zealander before, not even in the terrible Hihi, of Waimate. [Hihi was a well-known Nga-Puhi warrior and a very fleet runner. Much is to be found a})out him in " Wars of the Northern against the Southern Tribes in the Nineteenth Century.'"] I commenced to interrogate them, after having made friends with them hy means of some presents, when all of a sudden they quitted me abruptly, entered their canoe, and pushed off. Having inquired the reason of this precipitate retreat. I found that the Natives already on board, Shaki at their head, had insinuated to the companions of these two chiefs that my intention was to kill them, and that their lives were not safe on board the ship, wishing at all costs to drive them away. These cunning savages could not imagine a better means than this fiction, Smith. — Captain D'JJrville^s Visit to Toloya Bay 135 and it succeeded. Despite this treachery, and anxious as to the conse- quences it might have, I rebuked those who had invented the story, and hastened to disabuse the strangers, and asked them to come aboard again. They appeared to phvce faith in my protestations ; but, seeing that they had been deceived, they were exceedingly furious with the Natives on board, and although the latter were three or four times as numerous they defied them by words and the most outrageous gestures, and I saw that they challenged them to go ashore and render account for this insult. Those on board, gloomy and confused, hardly offered any words in reply. The strangers would not return on board, but demanded some hatchets of me in a tone of authority. I replied calmly that if they would bring some hogs on board they should not want what they desired. On that they moved off without further communication with us. I felt a sincere regret, for it would have been easy to have cjuestioiied them and learnt the reason of their superiority over our first guests. My first thought was that they belonged to a tribe at enmity ; but they had presented themselves in too few a number to have dared to defy the others on board as they- had done. Beyond that, the latter constantly denied that the former were their enemies ; they ended, indeed, by saying, on the contrary, that they were friends and relatives. I observed that my (juestions in regard to this matter did not please them — generally they eluded them — above all, Shaki, who did all he could to turn the conversation to another subject. In consequence of what I thoi learned of the manners and political constitution of these people, the following appears to me the most probable theory : As in all other parts of New Zealand, the Natives of Houa-Houa [Uawa] live in small independent groups, under the direction — or, rather, under the protection — of their own particular chiefs. Without doubt those who first arrived belonged to some feeble tribe, whilst those of the later canoe belonged to one more powerful, commanded perhaps by some redoubt- able ariki like Shougui [Hongi] at the Bay of Islands, and Poro on the north part of the Ika-na-Mawi [Te Ika-a-Maui]. The first-comers, fearing to see their neighbours take from them, in consequence of their credit and opulence, the treasures of Europe, and wishing to obviate loss, tried to avoid this by at first engaging us to fire on them, and afterwards by persuading them that my intention was to destroy them. Thus may be explained the arro- gance of the strangers, as well as the surprising patience with which the others listened to their reproaches and provocations. Among this people, as everywhere, a too-powerful ally is often more feared than an enemy that one might oppose with equal arms. Tlie only prepared head (nioko niohai) which we saw here was brought in that canoe, and purchased for a little silver, valued at about the price of a few beads of coloured glass. It had Ijeen well prepared and conserved, and had belonged to some distinguished person. It is a pity that it has not been taken to France, for it very well illustrated the fine type of the people, and the design of a complete tattoo. Here we mad the acquaintance of the Pihc [D'Urville had learnt this well-known funeral dirge on his previous visit to the Bay — it is printed in Kendall's "Grammar"], though Shaki could only recite some portions, M^hich he repeated uniformly, and often twenty or thirty times following. But Rau-Tangui [Rau-tangi], a very sprightly young woman of twelve or thirteen years, and who was singularly attached to me, recited it almost completely, as it is found in the grammar of the missionaries. Both 136 Transactions. were agreed in confirming the fact that it is the prayer addressed to the grand atua of heaven when the sacred food is offered on the field of battle. [Rather is it a dirge sung over the great dead.] Young Rau-Tangui appeared to be intimately connected with Shaki, but it was impossible for me to learn whether she was his slave or his sister. Their responses to my questions varied at each instant and left me in incertitude. With the system of adoption prevailing amongst them, it seems possible that both were correct, and that in fact the father of Shaki had espoused one of his prisoners, mother of Rau-Tangui. That little girl was extraordinarily lively ; her body was in constant movement, and her imagination was equally active, for we sav/ her laugh, then cry, and often do both almost at the same moment. Many of hex companions offered their favours indiscriminately to the officers and sailors for any kind of trifle ; but it is well to be on one's guard, for the :-e ladies, following their constant practice, not content with voluntary tributes given to them, added all they could steal. Thus one of our gallant chevaliers saw his watch disappear all at once, to his great consternation, and subsequently found it in the hands of the honest Shaki, for it is ordinarily to the supreme chief all these objects accrue. Our two passengers from Tera-Witi [Palliser Bay] had made acquaintance with the inhabitants of Houa-Houa [Uawa], and Tehi-Noui had decided to remain with them. I confirmed him in that resolution, and gave him, at his request, a cartridge of powder, in order to satisfy the rangatira under whose protection he pretended to be, and who was to furnish him with a canoe to enable him to return home. As a fact, after muskets (pou) [pu], more precious than gold or diamonds amongst us, powder is the object most essential in their eyes. Koki-Hore appeared little satisfied with this determination, preferring to remain on board, but honour prescribed that he should follow his chief. All the morning it had been nearly calm, and I hoped to pass the night tranquilly at anchor, when at 6 p.m., with a light breeze from the W.N.W., we found that our anchor was dragging. Twenty fathoms of chain that ■were paid out instantly did not stop us. I concluded that our anchor was foul. We were rapidly approaching the breakers of Moui-Tera (Sporing Isle of Cook), and I could not hope to let go a second anchor, for fear of exposing our cable to become fouled with the chain at the turn of tide. I decided, therefore, to get under sail and out of the bay. At the same moment our two boats came off, and my decision was without doubt the safest. There remained on board fifteen Natives, of whom five or six were females, who had allowed their canoe to depart, with the intention of passing the night with us. They were at first very much alarmed, and thought we were going to carry them off. I endeavoured to reassure them by explaining the reasons that forced me to quit the anchorage so hastily ; then they resumed their confidence and gave us a representation of one of their dances and passed the night in gaiety. Shaki, Rau-Tangui, and tM^o other rangatiras gave me very minutely the names of the different parts of the coast from Cape Gable (Pa-noui-Tera) [Pari-nui-te-ra] up to the East Cape (Wai-Apou). [Wai-apu River is about eight miles south of the cape in reality.] Sporing Island is Moui-Tera, and White Island, on the right of the bay in entering, is Motou-Heka. It is worthy of remark that the names of Tologa and Tegadou are quite unknown to the Natives ; but it has long since been averred that Cook, so full of sagacity otherwise, had little aptitude in acquiring the names of Trans. N.Z. Inst., Vol. XLI. Pl. XIII. Fig. I. Fig. 2. J^ ■ Z690 Fig. 3. D'URVILLE AT TOLOGA BAY. — Smith. Face p. 136. Trans. N.Z. Inst., Vol. XLI. Pr. XIV Fig. I. FlG. 2. Fig. 3. D'URVILLE AT TOLOGA BAY.^Smith. Smith. — Captain D'UrviUe's Visit to Tologa Bay. 137 the peoples he visited, and, above all, in representing them in writing.* The true name of the bay, Tologa, or, at least, of the district which sur- rounds it, is Houa-Houa [Uawa], and it is that which we have adopted. On the Isle Moui-Tera we were able to view at our ease those singular arches, formed by nature or the effect of the waves, which had already attracted the attention of Cook and his companions. I sincerelv regretted being constrained to quit this place so promptly, for I had promised myself much pleasure in making some excursions. To judge by the account of Cook and his companion Banks [Sir Joseph Banks, F.R.S.], the surrounding country is very picturesque ; and, beyond that, the Natives of the district, still practising their original customs, and barely as yet influenced by their intercourse with Europeans, would have been for me a subject of interesting study and observation. It was here that I obtained the first positive information on the subject of the kiwi, through a mat ornamented with plumes of that bird, and which is one of the first objects of luxury of the Natives. According to them, the kiwi is a bird of the size of a small dindon, but, like the ostrich and the cassowarv. deprived of all means of flight. These birds are common in the neighbourhood of Mount Ikou-Rangui [Hiku-rangi]. It is by night, with torches and dogs, they are caught. It is probable that these birds belong to a genera closely allied to the cassowary, and I believe it has already received the name of Aptenjx by some authors. M. Quoy brought me a leaf of a species of palm which I had already observed in Tasman's Bay. Unluckily, it had neither fruit nor flowers, so I have not been able to recog- nise to what genus it belongs ; all I can say is that I am inclined to believe it is allied to the Zamia or Seaforthia of Australia. It is the same vegetable without doubt that Cook designates " chou-palmiste " [? cabbage-palm], for there are no true " arequers '' [? areca palms] in these parts. The latitude which results from the observations of MM. Jacquinot and Lottin is found to be 33° 22' 32" S., which differs only 8" from that found by Cook ; and the longitude is 176° 5' 35" E. [east of Paris]. Although we did not remain long in this anchorage, I do not consider it other than as a good one, so long as there is no appearance of wind from the north to the east ; only it is necessary to anchor at a cable's-length or two more to the west, towards the bottom of the bay. I was prevented from doing so by the double desire to make sail easily and to be nearer to succour our people at the observatory if that became necessary.f 6th February, 1827. — A light breeze from the N.W. prevailed all night, and we passed it peaceably, lying-to in 35 fathoms, sandy mud. At 4.5 a.m. I sent the two smaller boats, under the orders of MM. Lottin and Dude- maine.t to measure a base in Houa-Houa Bav, the onlv element still wanted * This is perfectly true ; it is rare that Cook ever comes near the proper Native names of places, either in New Zealand or other parts inhabited by the Polynesian race ; whilst D'Urville is more often right than wi'ong. t M. Quoy (the celebrated naturalist) saj's. in x'cgard to Cook's Cove, Tologa, " That little bay is too open to lie much peopled. \Ve were surrounded by a considerable number of canoes, among which were some very fine ones, containing thirty paddlers. Their manner of i)addling is to sit, and this gives to these vessels as much elegance as majesty : they have no outriggers, and their bottoms are made of a single tree-trunk." . . . J M. Lottin describes his visit ashore to measure a base, as follows : " The calm which prevailed permitted the two boats to advance rapidly towards the bay. Our passengers attentively studied with curiosity each article in the whaleboat, and explained to each other its use, and their reflections thereon. Our long oars at first attracted their attention, and they followed with the head their regular movements, uttering 138 Transactions. by tlie first of those officers to complete his plan. At the same time I sent ashore twelve of the Natives mth whom we were still charged. Amongst that number were Tehi-Noui and Koki-Hore, who here took leave of us, and to whom I gave a quantity of powder — double that which I had pro- mised. In seeing them depart I had sincere wishes for their safe return. If they were destined to reach their own country, I felt sure they would soon forget their ennui on board, and that they would recall with pleasure the friendship and good treatment they had received. There remained on board only Shaki, Rau-Tangui, and two other chiefs, whom I was glad to retain in my power until the return of the two boats. At this time there arrived alongside a great number of canoes laden with provisions, which the Natives disposed of peaceably and with great good faith. They had many pigs, potatoes, and much Phormium fibre, all of which we bought at reasonable prices. Towards 11 a.m. the boats returned on board, and I hastened to put to sea to get rid of the Natives, whose cries and babbling with the crew commenced to be excessive. We parted very cries to excite the ardour of the sailors, and presently themselves giving a hand with noisy gaiety. They pulled so hard that, fearing to see the oars broken, I requested them to remain as spectators of the operations. One of them, with an expressive pantomime, undertook to demonstrate to us the superiority of their paddles over our oars ; these last seemed to them of an inconvenient length, and required sevei-al men to move a boat, whilst a single paddle would make a canoe fly, by using the paddle on alternate sides. Another Native observed that each sailor turned his back to the direction in which he was going, which made them all laugh heartily. Their attention was also drawn to other objects. The rudder struck them particularly, and they gravely con- sidered its utility, with frequent marks of a]>probation. The tiller was confided for a moment to one of them, and the ]n'omptitude with whicli it changed the direction of the boat in its rapid pace ravished them with admiration. I steered for the north point of the bay, a route which made us pass along the reefs that separate Motou-Heka [Motu- heka] and extend a mile and a quarter to the N.E. They form a line of rocks near which are to be found 7 to 11 fathoms of water; we passed within a few feet. These reefs are covered with several species of limpets, and I regretted not having time to land. Not having more than a few moments to pass ashore, I took from its case Rochon's micrometer. The brilliant colour of the brass suddenly attracted the atten- tion of the Natives. I placed before the eye-piece a coloured glass, and, holding it to the eye of my neighbour, I succeeded with some trouble in making him see the disc of the sun. He explained at once to his companions that he saw the sun coloured red. without being dazzled. I then replaced it with a green glass — another surprise. Lastly. I moved the crystal prism, and the disc appearing double excited a cry of astonishment. Each one desired to have the eye-piece in his hands, but we approached the land and their curiosity was thus not satisfied. I wished to debark our ]>assengers before a little village. Twenty houses and nine canoes haided up on the beach denoted a village of abotit one hundred persons. They came running dowii to receive us withotit arms. Some rocks bordering the coast prevented our coming close. They ottered to haul the boat on to the shore, which usage is probably considered an honour in this country, for our guests received the proposition with cries of joy. But I had no desire to abandon myself to the discretion of fifty strong and jolly fellows, who were alreadj^ in the water up to their waists. Seeing that they insisted. I made use of a ruse to get rid of them : I traversed rapidly an inlet somewhat deep, landed the Natives, took the micrometric distances whicli I wanted, and was in the boat again, to the great disappointment of the crowd, which had been forced to run round the inlet, arriving just in time to see us depart. Some young men defied us by chanting their war-song ; but we were by that time at ease, and there was not a single stone on the rocks, which the waves clear off each tide. I fired a shot to inform the second boat that our o]icrations were com- plete, and it rejoined me on the way to the corvette. M. Dudemaine. who commanded it, had been troubled by the Natives ; they, fully armed, surrounded the boat with their canoes, endeavouring to take anything which fell into their hands, and refusing obstinately to sell any of their arms ; the muskets, above all. excited their cupidity. The distance from the corvette rendered them daring, and no doubt if the boat iiad been alone they would have j)roceeded to some violence." ?■ Smith. — Captam D'Urvilles Visit to Toloqa Bay. 139 good friends, though they were much concerned to see that I would not return to Houa-Houa. I observed that the term " New-Zealander " is already employed in this district ; only, in lieu of " Noui-Tireni," as the Natives of the Bay of Islands pronounce it, they say " Noui-Tirangui " [Nui Tirangi], which gives the word more of an indigenous sound. The word pakeha serves them to signify all whites, whom they also call " louropi " (European). I did not observe that they had any special name for the English. They use ariki for a principal chief, and tohunga (prophet [sic]) appears unknown to them. We had nothing but feeble breezes from the north to north-east, with calms, which did not allow us to make much way. At about 3 p.m. a large canoe, which had for a long time been approaching us, came alongside. The principal person came on board, and accosted me with an ease and grace which proved that he was accustomed to deal with Europeans. He told me his name was Oroua [Te Rere-horua, in reality], and that he was the principal chief of the pa at Toko-Malou [Toko-maru], probably the Tegadou of Cook. This chief conserved the knowledge by tradition of the visit of that navigator to Houa-Houa and Taone-Roa [Te One-roa — Poverty Bay]. . I had Oroua to dinner with me, who appeared much flattered with that favour, and comported himself with perfect propriety. At my demand he recited very correctly the last part of the Pihc ; we spoke much of the different chiefs of the Bay of Islands, and he appeared well acquainted with the wars that di\"ided the northern people. After the repast he conjured me to anchor for at least twenty-four hours near his home. To induce me to do so he offered me gratuitously two fine pigs. I thanked him politely, and bought them for the ship. His canoe contained more than twenty of these animals, but as we had bought at Houa-Houa all that we could accommo- date no one wanted to buy there. Notwithstanding, the companions of Oroua were very desirous of selling, so as not to have to take them back, and therefore parted with them in exchange for knives. . . . [From Toko-maru the " Astrolabe " continued her voyage round the East Cape and to Whangarei without communicating with the shore. At the latter place we propose to take up D'Urville's narrative, and allow him to describe his visit to Wai-te-mata, the present site of Auckland. With regard to the two Natives, Te Hi-nui and Kiore, whom D'Urville landed at Tologa Bav, inquiries instituted in 1896 show that they finally made their way overland to their homes ; biit they must have run great risk, for at that time the devastating incursions of Waikato, Taupo, and Kgati- Rau-kawa had commenced and the Hawke's Bay country was not a safe one for strangers to travel in.] EXPLANATION OF PLATES XIII AND XIV. Plate XIII. Fig. 1. Village in Astrolabe Bay, Tasman Bay. Fig. 2. '■ L'Astrolabe" in the French Pass, 1827. Fig. o. Te Hiuui (on the left), Kiore (on the right). Pl.\te XIV. Fig. I. Cook's Cove and Sporing Islands, Tologa Bay. 1827. Fig. 2. Captain Cook's watering-place, Cook's Cove, Tologa Bay. Fig. 3. War-dance on board " L'Astrolabe," Tologa Bay, 1827. 140 Transactions. Art. XXIV. — Description of a Netv Species of Epilobium. By D. Petrie, M.A. [Bead before the Auclcland Institute, \%th November, 1908.] Epilobium Cockaynianum, sp. nov. E. herbaceum flaccidum csespitosum. Caules 10-15 cm. longi, erecti v. basi decumbentes, deinde ascendentes, plus minus ramosi, pallidi v. sub-erubescentes, bifariam puberuli, teretes, interdum superne omnino pubescentes. Folia floralibus exceptis opposita, conferta, 13 mm. longa, 8 mm. lata, tenuia, late ovata v. ovato-elliptica, obtusa, glabra, remote et obscure v. vix denticulata, breviter petiolata ; nervo medio baud prominente, nervis secundariis nuUis. Flores 1-3 in ramis singulis, in axillis foliorum superiorum dispositi, circa 6 mm. longi ; calycis laciniis lanceolatis, acutis ; petalis albis v. roseo- albis, calyce ^ longioribus. Capsularum pedicelli fructu maturante elongantes, demum 2-4 cm. longi, graciles, rubelli, plus minus puberuli. Capsula glaberrima, brunnea, 2^— 3| cm. longa ; testa glabra. Hab. : Mounts Hector and Holdsworth, in the Tararua Range, at 3,300 ft. and upwards ; very plentiful on Mount Holdsworth. The present species is most nearly allied to E. alsinoides, A. Cunn., and E. Hectori, Haussk. It is likely that the Ruahine Range plant referred by Cheeseman to the latter (" Manual New Zealand Flora," p. 177) properly belongs here. E. Hectori I believe to be confined to the South Island. Art! XXV. — Notice of the Discovery of a Species of Burmanniacese, a Family New to the New Zealand Flora. By T. F. Cheeseman, F.L.S., F.Z.S., Curator of the Auckland Museum. [Read before the Auckland Institute, ISth November, 1908.] The flora of New Zealand, as regards the flowering-plants, has now been so well explored, and its composition so well ascertained, that much novelty cannot be expected, although isolated discoveries ■will doubtless be made from time to time. Under these circumstances, the addition of another family of plants to those already known to occur in the Dominion cannot fail to excite considerable interest. No apology is, therefore, required for submitting the following notice of its discovery to the Institute. In January, 1903, Mr. H. Hill, of Napier, so well known from his numerous papers on the physiography and geology of the ceittral volcanic plateau of Cheeseman. — Discovery of a Swedes of Burmanniacete. 141 the North Island, forwarded to me a single specimen of a plant found by him at Opepe, near Lake Taiipo, which from its habit and general appear- ance I at once provisionally referred to the Burmannincece. Positive identi- fication, however, was quite impossible, as the whole of the interior of the flower, including the stamens, upper part of the ovary, and the style and stigma, had been removed through the attacks of some insect. The discovery induced me to make a special journey to Lake Taupo, in which I was accom- panied by Mr. Hill ; but, although a long search was made in the locality where the first specimen had been obtained, another damaged specimen was all that could be found. In January, 1905, I made another search for the plant at the southern end of Lake Taupo, but entirely without success. In January, 1907, Mr. Hill paid another visit to Opepe, accom- panied by Mr. A. Hamilton, of Wellington. On this occasion he was fortu- nate enough to find a considerable number of specimens in full flower, most of which he very kindly forwarded to me. An examination of these proved that the plant had been correctly referred to the Burmamiiacece, and that it must be included in the subfamily Thismiece, which differs from fhe rest of the Burmanniacecp in possessing both the inner and outer whorls of stamens, and in the unusually large development of the anther-connective. It further appeared that there was little to separate Mr. Hill's plant from the genus Bagnisia, as amended by Engler in " Die Naturlichen Pflanzenfamilien " (vol. ii., part 6, p. 48), where it is made to include both Bagnisia and Geo- mitra of Beccari (" Malesia," vol. i, pp. 249-50, tt. 10-12), the only differ- ence of importance being that in Bagnisia and Geomitra three of the perianth- segments are wanting, or reduced to mere rudiments ; whereas in the New Zealand plant they are^well developed, being quite half the length of the inner segments. In this respect it agrees with the genus Thismia, but differs in the inner perianth-segments being dilated and connivent at the tips, exactly as in Bagnisia and Geomitra. In the position of the stamens and the structure of the anther it agrees with Geomitra ; in fact, the anther- connective of Geomitra episcopalis, as figured by Beccari, very closely re- sembles that of the New Zealand plant. If, therefore, Engler is to be followed in merging Geomitra with Bagnisia, it appears to me that the New Zealand plant should be placed in the latter genus. In a recent number of the " Kew Bulletin " I have therefore applied the name of Bagnisia Hillii to the plant. It gives m.e great pleasure to associate Mr. Hill's name v/ith the species, as some slight recognition of the long-continued interest he has taken in New Zealand botany, and of his unwearied kindness in supplying both Mr. Colenso and myself with specimens of many interesting plants collected during his journeys in the interior of the North Island. The* following description will enable the species to be recognised : — Bagnisia (Geomitra) Hillii, Cheesem. in "' Kew Bulletin," 1908, p. 420. A minute colourless saprophyte, perfectly smooth in all its parts ; leaves wanting or reduced to minute scales. Rhizome creeping amongst humus at the base of tall forest-trees, sparingly or copiously branched, 5-10 cm. long, 1-1-5 mm. thick, fleshy, naked. Peduncles springing from the axils of minute fleshy bracts, 1-flowered, erect or curved, 0-5-1-5 cm. long ; bracteoles 3-7, alternate, .lanceolate or ovate-lanceolate, acute or acumi- nate, the upper gradually larger, 1-5 mm. long. Flowers solitary, terminal, large for the size of the plant, 1-1-7 cm. long, about 0-7 cm. broad, bright rose-pink when fresh. Perianth campanulate-lanterniform ; tube obovate- oblong, distinctly 6-12 costate ; outer perianth-segments smaller, free. 142 Transactions. linear or oblong, at first erect but ultimately spreading, sometimes abruptly recurved. Inner segments almost twice the length of the outer, linear- spathulate to obovate-oblong, connate or connivent at the tips, gaping in the middle, keeled on the back, with the keel produced into a subulate point at the tip. Stamens 6, affixed to the throat of the perianth-tube, shortly exserted, abruptly deflexed within the tube ; filaments very short, free ; anther-connectives much enlarged and expanded, connate into a membranous tube which is bilamellate at the apex ; anther-cells small, distinct, towards the base of the tube formed by the connectives. Ovary inferior, broadly obovoid, 1 -celled : placentas 3, free ; ovules very numerous ; style short, thick ; stigma 3-lobed, the lobes broad, almost quadrate, concave, trun- cate at the tip. Fruit unknown. Hah. — Primeval woods at Opepe, near Lake Taupo ; alt., 2,000 ft.; H. Hill. Flowers in January. Bagnisia Hillii is usually found on the mound of decaying leaves and humus which accumulates at the base of the trunk of the kahikatea pine (Podocarpus dacrydioides). On account of its small size it is easily over- looked, even in the flowering season, the flowers being often partially con- cealed by fallen leaves. Once noticed, however, the bright rose-pink colour of the flowers enables the observer to pick it with ease. Like many of the Bxirmanniacefje, the flower has a most bizarre appearance. The three inner perianth-segments, widely separated in the middle, but closing together and connivent at the tips, give it somewhat the appearance of a bishop's mitre, or perhaps of a lantern with three elliptical windows or openings. Li the bud, or in the newly expanded flower, the three outer segments partly close these openings, but they gradually spread outwards, and ultimately (judging from specimens in formalin) become sharply reflexed. The structure of the anthers is most peculiar, and deserves careful study. As stated in the description, the connectives are enormously enlarged, and are connate into a broad membranous tube, which, owing to the curious manner in which the stamens are deflexed. lies parallel with the inside of the perianth-tube, the tips of the connectives pointing to the base of the flower, and the minute anthers opening into the narrow space between the connective-tube and the wall of the perianth-tube. The connective-tube is split into two delicate lamellfe at the apex, and the outer lamella of each connective is 2-lobed, with a slender bristle arising from the bottom of the sinus. On the com- missure of each connective, but on the inner face of the lamella, is a small oblong gland. The inner lamella is very delicate, and has an undulate margin fringed with delicate cilia. It is difficult to see how pollination is effected, seeing that the minute anthers, which only produce a small quantity of pollen, are hidden away at the back of the connective-tube, in a narrow passage to which access can only be obtained through the small openings between the short filaments, just at the entrance of the flower, or by crawling up behind the connective-tube from the base of the flower. It is significant that many flowers are found partly eaten by insects. Can it be that the conspicuous coloration of the flower and its juicy texture attract minute insects, which, while destroying certain portions of it, pollinate the short stigma at the base of the flower ? It is much to be desired that some local observer would work out the fertilis- ation of the plant in detail. Considerable attention has been paid to the BurmanniacecE of late years, the American species in particular having been worked up by Warming, Marshall. — Some New Zealand Fossil Cepkalopods. 143 and by Urban in his elaborate " Symbolse Antillanse." Part 2 of the " Nachtrag " to Engler and Prantl's " NaturUcheu Pflanzenfamilien," page 72, contains a brief sketch of a new chHssification of the family, from which it appears that sixteen genera, with about seventy-five species, are now known. Nothwithstanding the small size of the family, it has a wide dis- tributioii in the tropics, its chief development being in Brazil and Malaya. Northwards, it stretches as far as China and Japan in Asia, and Virginia in America. In the Southern Hemisphere the New Zealand species appears to be the only one yet detected outside the tropics. The subfamily Thismiece, into which Bagnisia falls, now contains four genera and about fifteen species. Seven of these are from Brazil; the remainder come from Ceylon, Borneo, and New Guinea. The discovery of an additional species in New Zealand, so far removed from the two centres of distribution of the subfamily, is a decidedly unexpected and somewhat puzzling fact in geographical distribution. Art. XXVI. — Some New Zealand Fossil Cepkalopods. By Professor P. Marshall, M.A., D.Sc, F.G.S., University of Otago. [Read before the Otago Institute. H)th November. 1908.] Hochstetter first discovered the remains of cephalopods in the Jurassic rocks of Kawhia. He described the species of Ammonite as A. novo-zelandicus. Two species of belemnites were also described. In later years Hector has added several species of belemnites to those named by Hochstetter. The occurrence has been frequently recorded by Cox, McKay, and others in the rocks of the Hokonui Hills and of Kawhia. No descriptions of these have yet been written. The species here described were collected by Mr. R. Browne and the writer in the Hokonui Hills, behind Mandeville, and by Mr. Browne near Te Puti Point, in the Kawhia Harbour. The strata in the former locality have been classed as Permian or Triassic by Hector, and in the latter they have been regarded as Jurassic by all authorities. Broncoceras mandevillei. Diameter, 9J in. ; breadth, 3i in. Surface ornamented with longitudinal and transverse striae, giving a knotted appearance to its surface. Deeply involute. Some specimens slightly constricted towards the ventral surface ; others flattened. Siphuncle not discernible even in the best-preserved specimens. Siphonal lobe some- what acute, but less so than the interior lateral lobe. 144 Tranffacfions. Rather frequent in the Hokonui Hills. This appears to be the orgarism called in the Geological Survey reports '" Paleenautilus." Part of Sdtuke-line of Bi-oncoceras mavdevillei. Part of Suture-line of Avceiites hokunui. Arcestes hokonui, n. sp. Diameter, 2| in. ; breadth, Uin. Deeply involute, not compressed. Surface smooth, except for distant lines of growth. Phylloceras kawhise, n. sp. Diameter, 5| in. ; breadth, 2 in. Deeply involute, somewhat compressed. Shell smooth, except for rather distant lines of growth. No keel. iEgoceras brownei, n. sp. Diameter, 2 in. ; breadth, | in. Surface marked with transverse ridges, which bifurcate near the venter. Form Anarcestes-\\ke. n: Suture-line of ^F.goceras hi'OKUci. SuTUEE-LiNE OF PhylloceraK kairhi(('. Orthoceras brownei, n. sp. Diameter, H in. ; length, not known. Septa ^ in. apart. Surface smooth. Siphuncle not seen. Orthoceras otapiriensis, Hector (?). Diameter, 3 in. ; length, not known. Septa I in. apart. Surface smooth. Siphuncle not seen. This organism appears to be identical with Hector's Belemnites otapiri- ensis, which is described as in all cases of a phragmacone without any guard. He records this form as abundant in the Hokonui Hills, the locality from which this specimen came. It is remarkable that such genera as Broncoceras and Orthoceras should be found in strata of such late periods. The former is associated with such a curious assemblage of genera that it is extremely hard to suggest any period to which they could all belong. Among these genera are Ostrcea, Trans. N.Z. Inst., Vol. XLI. Pl. XIVa. ;6 7 4 ^era NEW ZEALAND FOSSIL CEPHALOPODS. -Marshall. Face p. 141 Broun. — Notes on Coleoptera from the Chatham Islands. 145 Grypluea, Trigoma, Halobia, and Spiriferina. Since several of these are not known in strata older than the Jurassic, it is probably right to class these strata as Jurassic, thereby ionoring the prosence of the archaic genera here meutioned. This conclusion seems all the more reasonable when the present isolated position of the Dominion is considered. It is quite possible that another period of isolation had terminated at the beginning of the Jurassic period. An old fauna which had lived on during the period of isolation Avould then be mingled with the invading newer and more vigorous types. Such an explanation might reasonably account for the rapid change in life- forms which has caused Sir James Hector to class a conformable series of rocks as of an age extending from Permian to Jurassic. Art. XXVII. — Notes on Coleoptera from the Chatham Islands. By Major T. Broun, F.E.S. [Read before the Auckland Institute, ISth November, 1908.] A COMPLETE list of the Coleoptera now proved to occur in these islands is given for reference. It is just possible that some other species may have been described by European authors, but the list includes all that were recorded by the late Captain F. W. Hutton and those whose descriptions follow the list. Eighteen species appear to be purely endemic at the Chathams ; the re- mainino- twentv-three were originallv found in New Zealand. All the genera were instituted for the reception of New Zealand species, with the exception of such as are more or less cosmopolitan — eight or nine altogether. None of the genera and species recently described by me from the Auck- land Islands are represented, so far as we are aware at present, at the Chatham Islands, but I feel confident that some, or closely allied forms, will be discovered ultimately. List of Coleoptera from the Chatham Island.s. Group Anchomenid^. 1. Anchomenus suhmetallicus, White, Man. N.Z. Coleopt., p. 2-1. 2. ,, chathamensis, Broun, sp. nov. Group Colymbetid^. 3. Rhantus pulverosus, Stephens, Man. N.Z. Coleopt., p. 1333. Group Staphylinid^. 4. Creophilus oculatus, Fabricius, Man. N.Z. Coleopt., p. 107. Group HlSTERID.^i. 5. Sternaulax zeaJandicus, Marseul, Man. N.Z. Coleopt., p. 162. 146 Transactions. Group Trogositid^. 6. Leperina wakefieldi, Sharp, Man. N.Z. Coleopt., p. 179. Group COLYDIID^. 7. Rhitidinotus squamulosus, Broun, Man. N.Z. Coleopt., p. 201. Group Hemipeplid.^. 8. Diafjrypnodes tvaJcefieldi, Waterhouse, Man. N.Z. Coleopt., p. 217.. Group LucANiD.E. 9. Lissotes capita, Deyrolle, Trans. Ent. Soc, 1873, p. 339. 10. Ceratognathus helotuides, Thomson. Man. N.Z. Coleopt., p. 254. 11. MitophyUus reflexus, Broun, sp. nov. Group Melolonthid.^. 12. Odontria zealandica, White, Man. N.Z. Coleopt., p. 270. Group Elaterid^. 13. Thoramus wakefieldi, Sharp, Man. N.Z. Coleopt., p. 280. 14. ,, Icpvithorax, White, Man. N.Z. Coleopt., p. 282. 15. Mecastrus convexus, Sharp, Man. N.Z. Coleopt., p. 293. 16. Psorochroa granulata, Broun, Man. N.Z. Coleopt., p. 773. Group Clerid^. 17. Phymatophcea electa, Pascoe, Man. N.Z. Coleopt., p. 331. Group Heleid^. 18. Cilibe pascoei, Bates, Man. N.Z. Coleopt., p. 372. 19. ,, saragoides, Pascoe. 20. ,, subcostatus, Sharp, Ent. Mag., April, 1903. Group (Edemerid^. 21. Sessinia strigipennis, White, Man. N.Z. Coleopt., p. 120. 22. Thelyphassa diaphana, Pascoe, Man. N.Z. Coleopt., p. 122. Group Otiorhynchid^. 23. Cecyropa tychioides, Pascoe, Man. N.Z. Coleopt., p. 137. 21. Inophloeus traversi, Pascoe, Man. N.Z. Coleopt., p. 139. Group Erirhinid^. 25. Stephanorhynchus purus, Pascoe, Man. N.Z. Coleojit., p. 163. Group Cryptorhynchid^. 26. PsephoJdx sulcatus, White, Man. N.Z. Coleopt., p. 179. 27. Aldonus hylobioides, White, Man. N.Z. Coleopt., p. 183. 28. ,, chathamensis, Sharp, Ent. Mag., April, 1903. 29. Pseudoreda tibialis, Broun, Man. N.Z. Coleopt., p. 182. 30. Acallcs fougeri, Hutton, Trans. N.Z. Inst., 1897, p. 157. Broun. — Notes on Coleoptera fro)n the Chatham Islands. 147 Group PLATYPIDiE. -3J. Platypus apicalis, White, Man. N.Z. Coleopt., p. 541. Grovip Cerambycid.5. 32. Zon'nn minution, Fahricius, Man. N.Z. Coleopt.. p. 584. :33. ,. opacum, Sharp, Ent. Mag., April, 1903. 34. Xuthodes punctipennis, Pascoe, Man. N.Z. Coleopt., p. 580. 35. ,, divergens, Broun, Man. N.Z. Coleopt., p. 581. Group Lamiid^. 36. Xylotoles costatus, Pascoe, Man. N.Z. Coleopt., p. 599. 37. „ traversi, Pascoe, Man. N.Z. Coleopt., p. 599. 38. „ schauinslnndi. Sharp. Ent. Mag., April, 1903. 39. ,, ahnormalis. Sharp, Ent. Mag., April, 1903. 40. Hyholasius trigonellaris, Hutton, Trans. N.Z. Inst., 1897, p. 158. 41. Tetwrea ciJipes, White, Man. N.Z. Coleopt., p. 609. List of Lx'iroduced Species. Aphodius granarius \ Lacon murinus [ Recorded by the late Captain F. W. Hutton, Trans. Otiorhynchis suJcatus |' N.Z. Inst"!. 1897. pp. 156-58. Coccinella 1 l-punctafa ' Group Anc'homenid^. Anchomenus chathamensis, sp. nov. Suhoblong, slightly convex, nitid, piceous ; the legs, antennae, and palpi rufo-piceous ; lateral margins of thorax and elytra similarly rufescent. Head oviform and, including the large eyes, rather broader than front of thorax ; irregularly rugose behind the inter-antennal groove, smooth on the back part. Labrum large, entire. Antennae with the basal 3 joints shining and glabrous, 2nd joint half the length of the 3rd. Thorax one- fourth broader than long, its sides with well-developed margins, moderately rounded, very gradually narrowed behind the middle, posterior angles nearly rectangular but obtuse, the base feebly rounded towards the sides, apex incurved ; disc moderately convex, with feebly impressed stria? across it, dorsal furrow indistinct near the base and apex, near the front there is an indistinct transverse impression, basal fossae large. Scutellum smooth. Elytra oblong, slightly and gradually widened backwards, slightly sinuate but evidently obliquely narrowed towards the apices ; shoulders a little curvedly narrowed, yet rather wider than the base of thorax ; the suture is somewhat elevated posteriorly, the 4 discoidal stria? on each elytron are well marked but impunctate, the outer ones are finer, 3rd interstices tri- puncta te. Tarsi setose, the anterior spongy underneath, their basal 2 joints moderately dilated and oblong, the 3rd also dilated but shorter and more narrowed near the base, 4th small and cordiform, basal joint of the posterior grooved along the outside. Palpi rather short, terminal articulation sub- cylindric. Underside shining piceous, last ventral segment very broadly rounded, almost truncate, with a single setigerous puncture near each side at the apex. 148 Transactions. (? . Length, 3f lines ; breadth, 1| lines. Chatham Islands ; February, 1907. One example, forwarded by Dr. W. B. Benham for identification. It is somewhat similar to A. lawsoni, but smaller and more depressed, the sides of the elytra more explanate behind, the thorax relatively larger and less rounded laterally ; frontal foveae indefinite, &c. Group ^EsALiD.i:. Mitophyllus reflexus, sp. nov. Oblong, rather elongate ; subdepressed, subopaque, piceo-rufous, margins of thorax and elytra and the legs infuscate red, sparingly clothed with flavescent setae ; antennae, tarsi, and palpi red. Head much narrowed behind the large and very prominent eyes, broadly depressed between the greatly elevated antennal tubercles, closely punctate. Mandibles rather small and broad, bifid at apex. Antennae well developed, basal joint elongate, stout and much curved, 2nd very short, joints 3 and 4 ecjually elongate, 5th evidently shorter than the preceding one, 6th very short, 7th short and slightly prolonged towards the front ; club composed of 3 long lobes, bearing numerous slender outstanding setse. Thorax trans- verse, anterior angles obtusely rounded, the posterior rectangular : its sides explanate and obviously reflexed, apex subtruncate, base widely bisinuate ; its sides almost evenly rounded, yet a little narrowed towards the front ; its surface distinctly and closely punctured, less closely at each side of the middle in front, and having at the base a narrow elongated smooth space. Scutellum large. Elytra oblong, parallel-sided, with a depression inside each shoulder ; they are closely and distinctly punctured, and exhibit 3 or 4 feebly impressed longitudinal striae. Tibiae elongate, the intermediate curvate and finely asperate, the anterior subserrate externally, with a very small denticle above the middle and not in the least protuberant at the extremity. Tarsi slender and elongate, basal joint of the posterior short, 2-4 decrease in length, all however unusually long, the terminal slender and as long as the preceding 3 united ; claws very long and slender. 3 . Length. 4^5 lines ; breadth, 1^-2 lines. Chatham Islands. Described from two specimens found by Professor W. B. Benham in February, 1907. They differ in almost every detail from the typical New Zealand species {M. irroratus). The very prominent eyes, explanate and reflexed thoracic margins, and strongly elevated antennal tubercles are sufficient for immediate identification. Cilibe saragoides. Oblong-oval, moderately convex, subopaque, piceous, elytra more rufescent, tarsi and antennae pitchy-red. Head closely punctate. Thorax transverse, its sides broadly concave, with reflexed margins, gradually narrowed towards the anterior angles, which extend beyond the front of the eyes, near the base they are straight, the posterior angles being subacute, directed backwards, and resting on the elytra ; base slightly and widely bisinuate, the apex deeply incurved ; the disc finely and not closely punctured, more closely and coarsely but not deeply at the sides. Scutellum broadly triangular, with a few minute punctures. Elytra transversely convex, their sides very broadly expanded and reflexed, becoming less so near the middle, still narrower behind, and Broun. — Notes on Coleoptera jrom the Chatham Islands. 149 simple at the extremity, the base is broader than that of the thorax, tJiey are slightly but widely giniiate before the middle femora ; the broad grooves are opaque, with irregular punctures, so that the finely punctured interstices, which are slightly shining, appear somewhat costiform ; the broad marginal channels are indistinctly sculptured, there is no perceptible granulation ; near each side, at the base, there is a broad impression, which, however, may not be a constant character. The broadly expanded sides distinguish this species. Length, 5|- lines ; breadth, 2| lines. Pitt's Island. My specimen was presented to me over twenty years ago by the late F. P. Pascoe, who, no doubt, had described it under the name I have attached to it ; its description, however, I have not seen. Descriptions of Coleoptera from the Chatham Islands, by Dr. D. Sharp, copied from the " Entomologists' Magazine " for April, 1903. Group Heleid^e. Cilibe subcostata. Nigra vel picea, minus depressa, fortiter sculpturata, opaca, elytris evidenter subsulcatis. Long., 1.3J mm. This is distinguished from all the other species by the peculiar sculpture of the elytra, which, however, is only an exaggeration of what we find in some other forms. The front angles of the thorax are much produced, and the sides are much explanate, their margins a little sinuate ; the hind angles much produced backwards and markedly acute ; the punctuation at the sides is very dense, on the disc it is scanty, but the surface is not in the least shining. The elytra are rather short, and have a vague costation, the very slightly elevated ribs are separated by coarse punctures ; this sculpture sets off and makes evident the ribs. Professor Schauinsland found a small series of this species. It is nearest allied to C. pascoet, Bates, of Pitt's Island, a species which was also met with there by the German traveller. C. pascoei is, however, rather more elongate and less convex in form, and with the sculpture of the elytra different, there being merely traces of the longitudinal ribs. Professor Schauinsland's specimens are intensely black, being considerably darker in colour than Mr. Bates's type. I have dissected the sexes of C. subcostata, and do not find any external marks to distinguish them. Group Cryptorhynchid.t:. Aldonus chathamensis. Ferrugineus vel piceus, setis erectis numerosis superne vestitus, hand squamosus, rude sculpturatus ; subtus setosus, inter setas squamis perpaucis munitus. Long., 7|-13 mm. Distinguished from A. hylobioides and all the other species ascribed to the genus by the absence of scales from the surface. The rostrum is longer than it is in A. hylobioides ; it bears fine erect hairs, but in consequence of the absence of scales its coarse sculpture can be distinctly seen. Thorax very rough, with tubercular sculpture, with fine, short, erect hairs, and with 150 Transactio7is . still shorter, very slightly curved, thicker, more pallid setae, which represent the squamosity that is so remarkable in the other^ species. The elytra are rather deeply striate, and the stria? have very large punctures, separated only by short intervals one from the other. Chatham Islands ; Professor Schauiusland. Group Cerai'BYCid.^. Zorion opacum. Fusco-testaceum, supra submetallico-nitens, sericeo-subopacum ; antennis pedibusque testaceis, his femoribus basi excepta rufo-obscuris, illis fusco- annulatis ; elytro singulo ante medium fascia pallida transversa marginem lateralem fere attingente. Long., 4-5 mm. This comes very near to Z. minutum, but is distinguished by the peculiar pallid suffused colour and the silky dullness of the surface. The thorax, instead of being polished, is dull, and covered with a slight sculpture, a sort of minute wrinkling of the surface. The elytra are rather longer than in the other species. Chatham Islands ; Professor Schauiusland. Three specimens. The British Museum collection includes a specimen of this species said to be from Otago. This locality I think very doubtful. Group Lamiid.^. Xylotoles schauinslandi. Fusco-rufus, supra viridescens, nitidus, antennis pedibusque rufis ; elytris tricostatis, costis at apicem fere dualis, interstitiis irregulariter interruptim costatis. Long.. 10 mm. This species comes very naturally between X. traversi and A', costatus. It is not half the size of the latter ; but is a little longer than X. traversi, more elongate, with the sculpture more developed, and the costation con- tinued near to the tip. Of the forms found on the mainland, it is perhaps nearest to X. rugicoUls, but it is very different in colour, and the elytra are singly rounded at the tip. The thorax is elongate and subcylindric, and bears 2 transverse channels ; otherwise it is very indistinctly sculptured. The seutellum is covered with pallid pubescence. The elytra have each an elevated rib running along the suture, and outside this 3 others, the space between bearing much coarse irregular sculpture ; the 3rd costa is itself divided behind the shoulder so as to fork somewhat, and form, in fact, 2 costee. The ventral segments hav-e each a conspicuous spot of yellow pubescence at the side. The four specimens found by Professor Schauiusland differ but little, and the British Museum collection has two others. Chatham Islands ; Professor Schauiusland. Xylotoles abnormalis. Minutus, brevis, testaceus, pnllidus, tomentosus ; thorace fortiter trans- versus ; corporis latera longitudinaliter fuscuscente. Long., 5 mm. This minute Lamiid looks like a Ilyholasius. but as it is flightless I place it in Xylotoles, where it will come near to A'. hiiUoni. The front of the head is very low, and the moutli much inflexed. The antenna:^ have the 3rd Broun. — Revision of the New Zealand Cossouidae. 151 and 4th joints very elongate, the 4th a little the shorter, but quite twice as long as the 5th ; from this to the end each is slightly shorter than its prede- cessor. The thorax is scarcely so long as broad, infuscate at the sides and across the middle. The after-body is short, the elytra covered with minute tomentum, which allows, however, numerous small pits to be seen ; they are pallid, but at each side there is a large irregular dark patch, which be- yond the middle approaches near to the suture. Under-surface infuscate. Femora short and thick, yellow, with dark marks. Chatham Islands ; Professor Schauinsland. Two specimens. Art. XXVIII. — Revision of the New Zealand CossonidiB, with Descriptions of New Genera and Species. By Major T. Broun, F.E.S. [Read before the Auckland Institute, l^th November, 1908.] Owing to the difficulties encountered by local entomologists in identifying the numerous species, nearly all small, often without very perceptible dis- tinguishing characteristics, and, as a rule, inconspicuous and uninteresting, I determined to undertake the task of revision. The resolution was easy, the accomplishment just the reverse. Any naturalist who has really studied these minute creatures will readily acknowledge that the work of rearranging and classifying such a complex assemblage was an undertaking of more than ordinary difficulty. A distinguished British entomologist, with the best typical collections of insects and books of reference in the world easily accessible, when dealing with about twenty species of a nearly aUied group consisting of 108 genera, remarked that " the study of these genera is attended with great difficulties, for they are divided from one another by no strongly marked peculiarities," &c. So, although he stated that these twenty species represented " a con- siderable number of distinct genera," only two new genera were described, all the other species being referred to the typical genus of the group, and there. they have remained for upwards of thirty years. As the members of that group are much larger, and differentiated by more easily seen characters, it is unlikely that our Cossonidce would be more systematically dealt with. In 1873 no less than 123 genera, including five from New Zealand, were known to occur in various parts of the world. A great many of these are rare, and, as there is nothing very attractive about their general appearance, most collectors during their travels make no special search for them, con- sequently any New Zealand student will find it nearly impossible to obtain accurately named specimens of more than a dozen of these exotic genera for comparison with our own, so that in attempting to classify and name our indigenous species he must carefully study the Latin descriptions of these 123 genera. Any naturalist who has made the experiment will know what that means. 152 Transactions. Pentarthriwi may be accepted as the typical genus of our Cossoniclce, and to it, by European entomologists as well as by myself, over forty of our endemic species have been ascribed within the past thirty or forty years. These I have, so far as specimens were available, carefully studied, separated into groups or series, and detached first one and then another as representa- tives of new or distinct genera, until at length I had instituted seventeen new genera for their systematic location, irrespective of thirteen I had previously described. Only fifteen species have been left under the name Pcntarthrum, and these are divided into three sections, so that the identifica- tion of the older species has been much simplified. Few are aware of the trouble involved in that process. Every specimen in my collection was carefully set out and gummed to strips of cardboard or mica slabs, and after the superficial examination of generic characters had been completed it was necessary to remove each one from its original position, so that the structure and sculpture of the under-surface might be as carefully studied as that of the upper before the description of any genus could be properly prepared. This removal from the cardboard, and the subsequent replacement of the specimens in my cabinet, was a very tedious, delicate, and risky operation, as the least carelessness would result in the damage or loss of the type of some species which may not be found again during my lifetime. Notwithstanding all the care bestowed, I managed to lose one, much to my regret. On reference to the following list, it will be seen that our CossonidcB now consist of forty-seven genera, comprising 141 species, the descriptions of which are attached hereto. It must, however, be understood that the object in view was not to monograph the species, although each one has been more or less critically reviewed, and placed, in accordance with my own views, in its proper posi- tion. Every genus and its typical species have been fully described by myself, and two or three diagnostic characters of the species attached to each genus have been given as an aid to identification, together with references to the original descriptions. The maximum measurements are given ; that of the length invariably includes the rostrum of all properly mounted specimens. During the progress of the work I found that, for the convenience of colonial entomologists, it would be expedient to adopt some fixed standard for purposes of comparison. Pentarthrum zealandicum, var. canaliculatiwi, has been selected, and placed at the head of the list, because it is our typical exponent of the Pentarthrides, and also on account of its being readily pro- curable in the South as well as the North Island. Its generic description has been renewed and somewhat restricted, the term " more or less elon'gate,'' appUed to the rostrum in the original diagnosis, having been deleted, so that only such characters as are exhibited by the endemic species itself are given. Those who have no special knowledge of our Cossonidce should, before attempting to classify and name their collections, carefully study the general form, appearance, and structural details of the insect 1 have chosen as the standard, the female as well as the male. To do this thoroughly four speci- mens should be obtained, and one of each sex neatly set out and mounted on cardboard with the antennae, legs, and tarsi properly displayed, and another of each sex mounted on its back, so that differences of the under- side can be examined. Euophryum or Torostoma may be shidied next, noting and comparing the peculiar modifications of the rostrum and elytral Broun. — Revifnon af the yew Zealand Cossonidae. 153 margins ; then the common pubescent Sericotrogus, comparing the form of its head, the position of the coxpp, and structure of the lower surface with those of the standard. The training of the faculty of observation thus acquired will be invaluable when the specific names of. members of the more complex or rare genera have to be decided by the examination of single examples. \Mien reading descriptions the inexperienced entomologist should re- member that what is termed coarse sculpture, or vestiture, in the case of a minute insect would be considered to be only moderate, or even fine, in one of greater bulk. Mistakes are liable to occur through forgetfulness to make due allowance for such details. In the descri])tive portion of this memoir the habitat of every species, so far as known to me, has been recorded, but, as no reference has been made to modes of life, som.e brief remarks on this subject may be of interest. The greater number have been obtained promiscuously by being dis- lodged from shrubs or branches of trees at times when special notes of their capture could not be recorded, others were found under bark or adhering to the underside of logs, and a few were cut out of solid wood. Several very curious, though small, genera and species — two of them blind, or nearly so — are only found amongst decaying leaves, on the ground. The genus Pselactus, consisting of two species, and the last three attached to Eutornus, are inhabitants of the sea-shore. The three species of Novitas seem to live almost wholly on Phormiurn tenax, and one of Pklceophagosoma was taken out of the seed-vessels of that plant. Our native palm, Areca sapida, has yielded no less than four remarkable genera, but in order to search for and secure these I had to cut down more than one of the palms with my tomahawk, and to break off and carefully examine each frond separately. The most important genus, from a commercial point of view — Xenocnema — occurs in Agathis [Dammara) australis. Its destructive propensities M^ere observed by me over thirty years ago. The paper prepared regarding its ravages will be found in vol. ix, page 366, of the " Transactions of the New Zealand Institute." LIST OF THE NEW ZEALAND COSfiONIDM. No. PBNTARTHRIDES. Pentarthrum, Wollaston. 903. zealandicum. ^^'ollastoll 2195. amicum, Broun 2189. fuUoni, Broun 1627. proximum. Brovui . . 911. hrevirostre, iSharj) . . 1304. ruficorne. Broun philpotti. Broiui 1548. melatiosiernum, Broun 1300. puHCtirostre. Broun planicoUe, Broun * . . 905. subsericalum. Wollaston 909. assimihttum. Broun 1298. rediictum, Broun 907. bninneiim, Broun . . 2191. nubilum, Broun Toiiropsis, Bi'oun. 925. pi()icf((tiis, Broun . . Page No. Eiiophrymn, Broiui. Page 908. ntfum, Broun 160 156 1301. aspereUuni, Broiui . . 160 156 1297. scuJpturatum, Broun 160 156 2194. pimctatissimum. Broun 160 156 dnhitans, Broun . 161 157 1299. confinum, Broun . 161 157 antennale, Broun . . . 161 157 crassellum, Broini . . 161 1.57 1629. ■semi I urn, Broun 161 . . 157 2198. porcatiim, Sharp 161 158 . . 157 Zenoteratus, Broun. 158 158 1549. maciucephalus, Broun . 162 2190. diversus, Broun 162 158 158 2197. cephnlotes. Sharp . . . 162 159 Torostoma, Broun. 906. (iptcate, Broun 163 154 Transactions. Toura, Broun. Page hngirostre, WolLaston . . 164 fiilva. Broim . . . ■ 164 morom, Bioun . . . . 165 Merisma. Broun. slmrfiana, Wollaston . . 165 (lurdniiaca, Broun . . . . 166 Tanysowa. Broun. e.s. Broun .. .. 192 Heteropsis, Wollaston. 940. /«(c.vc are inserteci midway between the middle of the rostrum and the eves. 160 Transactions. Euophryum rufum, Broun. 908. Man. N.Z. Coleopt., p. 510. (PLate XV, fig. -^) Subcylindric. slightly nitid, piceo-rufous. seemingly calvous, but with some minute greyish hairs ; antennae and tarsi paler. Rostrum distinctly and rather closely punctate ; the vertex more coarsely. The smooth occiput distinctly marked off immediately behind the eyes. Scape much shorter than funiculus. Thorax with obtuse hind angles, rather gradually narrowed anteriorly, only moderately constricted near the apex and causing a transverse impression there ; it is coarsely, rather closely, and on some parts longitudinally confluently punctured, very closely and rugosely at the sides, much more finely at the apex. Elytra quite parallel, longer than but hardly as broad as the thorax ; dis- tinctly and rather closely punctate - striate, interstices with fine serial punctures and sometimes a little rugose. Underside moderately shining, sparingly and minutely pubescent, some- what irregularly, moderately coarsely, but not very closely punctured. Metasternum slightly flattened and distantly punctured along the middle, with a small angular fovea behind. Basal ventral segment flat, with two slight obtuse elevations behind, separated by a broad groove; 3rd, 1th, and 5th with a transverse series of distinct punctures on each. Female. — Rostrum more finely punctured than the male. S . Length, nearly If lines ; breadth, f line. Mount Manaia, AVhangarei. Both sexes in my own collection. E. asperellum, Broun. 1301. Man. N.Z. Coleopt., p. 732. Nigro-piceous, antennae and tarsi rufo-piceous, slightly nitid. Rostrum rather longer than that of 908, eyes evidently more prominent. Thorax longer and more closely punctured, without the least trace of any smooth median line. Elytral striae crenate-punctate, interstices rugose. $ . Length, 2J lines ; breadth, | line. Wellington. Unique. E. sculpturatum, Broun. 1297. Man. N.Z. Coleopt., p. 731. Rufo-piceous. Rostrum slightly narrowed from the antennae tow^ards the extremity -, distinctly, very closely, and somewhat rugosely punctured throughout, with a transverse impression midway between the antennae and extremity. Scape very short. Thorax with an ill-defined smooth median line. Liner extremity of tibia^ with an acute denticle. 3 . Length, 1|- lines ; breadth, | line. Parua, Whangarei. Unique. E. punctatissimum, Broun. 2194. Man. N.Z. Coleopt., p. 1246, Near 1297. Rostrum not narrowed anteriorly, rather shorter, more transversely convex, not impressed near the front. Scape even shorter and thicker. Inner angle of anterior tibiae more acutely projecting, the tibia itself some- what curved externally, the femora slender near the base but strongly arched above. Eyes very convex. Moderately shining, thorax dark red, elytra obviously paler. S . Length, 1| lines ; breadth, | line. Howick. Both sexes. Bkoun. — Revisio)i of the Xew Zealand Cossonidae. 161 E. dubitans, Broun. Description being printed at London. Near 908, S- Rostrum slightly longer, rather more finely and closely punctured. Club distinctly longer, not much broader than 5th joint of funiculus. 3 . Length, nearly 2 lines ; breadth, | line. West Plains, Southland. E. confinum, Broun. 1299. Man. N.Z. Coleopt., p. 732. Rufo-piceus, pubescence yellowish and scanty but quite easily seen. Eyes more prominent than those of the female E. rufum, the shape a little more fusiform, punctuation of rostrum almost seriate, the inter- ocular area not raised above the level of the front of the occiput as in that species. 2 . Length, If lines ; breadth, f line. Wellington. Unique. E. antennale, Broun. Ann. Mag. Nat. Hist., 6, xv, p. 415. Pubescence slender, yellowish, quite perceptible. Body slightly more fusiform than that of 908, scape rather longer, club evidently narrower, punctuation on the middle of thorax more open with larger smooth intervals. g . Length, 1| lines ; breadth, f line. Invercargill. Both sexes. E. crassellum, Broun. Ann. Mag. Nat. Hist., August, 1904, p. 123. Rufo-piceous, cylindric, minutely pubescent. Club narrow, but little broader than 5th joint of funiculus. From the female of 2194 it is distinguished by the more robust form, darker colour, more distinctly punctured rostrum, and less rugosely sculptured thorax. E. foratum can be separated by the absence in it of interstitial punctures and hairs. ? . Length, 2 lines ; breadth, | line. Picton. Unique. E. servulum, Broun. 1629. Man. N.Z. Coleopt., p. 911. Differs from the corresponding sex of 908 by the more shining surface and much finer thoracic sculpture, rather longer and more slender antennae, less prominent eyes, &c. $ . Length, IJ lines ; breadth, -| line. Taieri, Otago. Unique. E. porcatum, Sharp. 2198. Man. N.Z. Coleopt., p. 1248. Subcylindric, piceous, nitid. Eyes prominent. Thorax coarsely and very closely punctured. Elytra deeply punctate-striate. Its description shows that it is the only species of this genus without interstitial punctures and pubescence. I have not seen it. Length, nearly 2 lines. Dunedin, Greymouth, and Picton. Zenoteratus, gen. nov. Body cylindrical, transversely convex ; pubescence minute, scanty, and inconspicuous. Rostrum short, broad, parallel, and half the width of the head in both sexes. Head almost abruptly enlarged and of almost equal 6 — Trans. 162 Transactions. breadth throughout, nearly as long as the rostrum, globose below. Eyes widely distant from each other and from the thorax. Antennfe medially inserted in the male, behind that point in the female. Scape short, attaining the back of the eye. Funiculus 5-articulate, 2nd rather shorter than 1st yet evidently longer than 3rd, 3-5 transverse. Club broad, but compressed, so that it seems hardly broader than the funiculus when examined sideways. Thorax widest near the base, much narrowed towards the front, where it is only moderately constricted. Scutellum small. Elytra parallel, posterior margins expanded, the dilatation, however, is partially concealed by the thickened lateral interstice just above it ; they are singly rounded and slightly dehiscent at the extremity. Legs stout; tarsi narrow, 3rd joint not lobate. When compared with the typical Pentarthrwn, 903, the large swollen head is very apparent, the eyes are more widely separated, the rostrum is shorter, and in the female much shorter and broader ; the scape is shorter. The apical portion of the elytra is manifestly different, and when examined from the side or underneath is seen to extend downwards and to be on an obviously different plane from the last three ventral segments, appearing more like one of the Brenthidce. The anterior coxae are more widely separated. Zenoteratus macrocephalus, Broun. 1549. Man. N.Z. Coleopt., p. 869. (Plate XV, fig. 3.) Piceous or nigrescent, legs and antennae piceo-rufous. Rostrum moderately finely and closely punctured, with a slight broad longitudinal impression behind, bearing yellow setae in front. Head convex, not closely punctate, the occiput more finely and remotely. Thorax nearly a third longer than broad, appearing somewhat swollen behind, the disc moderately finely and not closely punctured, the linear median space and apical margin nearly smooth. Elytra punctate-striate, interstices with dis- tinct serial punctures, in some aspects appearing a little rugose. Underside as shining as the upper surface and bearing slender but distinct yellowish hairs, moderately punctate. Metasternum elongate, flattened behind, with a median sulcus. Basal ventral segment slightly impressed, its sinuate apical suture fine, 3-5 on a lower level than the basal two. Female. — Rostrum scarcely longer and only a little narrower than in the male, rather more finely sculptured. J . Length, 1| lines ; breadth, f line. Taieri, Mount Arthur, Waikato. Both sexes. Z. diversus, Broun. 2190. Man. N.Z. Coleopt., p. 1244:. Shining, ferruginous, -club fulvescent. Thorax with an indistinctly raised smooth central line, and with an impression in front of the scutellum similar to that seen in Z. macrocephalus. Elytra biarcuate at base, punctate-striate, the 3rd and 4th striae indistinct near the middle, suture and interstices with fine serial punctures, interstices not rugose, more or less elevated behind. 2 . Length, If lines ; breadth, f line. Clevedon, Hunua Range. Unique. Z. cephalotes, Sharp. 2197. Man. N.Z, Coleopt., p. 1247. Subcylindric, piceous, nitid. Thorax closely and finely punctate. Elytra very deeply striated, coarsely Broux. — Bc'visinn of the Xew Zealand Cossonidu\ 163 and closely punctured, the punctures confluent, the interstices narrow, in- distinctly seriately punctate. 2 . Length, nearly 1| lines : breadth, | line. Picton. Evidently closely allied to 1549. I have not seen it. Torostoma, gen. nov. Robust, subcylindric, narrowed anteriorly, transversely convex, sparingly and indistinctly pubescent. Rostrum twice as long as broad, parallel or jiist perceptibly narrowed anteriorly, on the same plane or slope as the head, which, at the sides, is. slightly constricted immediately behind the eyes. The scrobes are deep and oblique towards the lower part of the eyes. Scape medially inserted, of moderate length, attaining to just behind the centre of the eye. Funi- culus with the 2nd joint nearly as long as the 1st, 3-5 transverse. Club moderate, oviform. Eyes prominent, more so behind than in front. Thorax longer than broad, curvedly narrowed towards the frontal constriction. Scutellum small. Elytra parallel, of the same width as the thorax ; posterior margins rather widely dilated and appearing each as two curves ; under- neath the dilatation is broad and distinctly sculptured from the 3rd ventral segment to the extremity, and on an evidently higher level than the terminal 3 segments. The margins of the buccal cavity are thick, and, in line with the cunei- form mentum, ternainate as tubercular projections. The rostrum is broadly concave underneath, with thick borders. The metasternum is elongate, depressed behind, and grooved along the centre. The basal 2 abdominal segments are on a higher plane than the following 3 ; the first is medially depressed. Femora strongly inflated ; tibire much curved, with well- developed hooks ; 3rd tarsal joint simj^le. The characters of the underside as detailed above, in conjunction with the peculiarly dilated elytral margins, distinguish this genus in an unmis- takable manner from Pentartkrum and its allies. Torostoma apicale, Broun. 906. Man. N.Z. Coleopt., p. 509. (Plate XV, fig. 4.) Nigro-piceous, moderately nitid, legs piceous, antennae and tarsi dark red ; sparingly and indistinctly pubescent. Rostrum moderately finely and closely punctured, the interocular sculpture nearly similar, occiput with many minute punctures. Antennae pubescent. Thorax convex, moderately closely and in proportion to the large size of the insect not at all coarsely punctured, the apex more finely. Elytra cylindrical, moderately striate, the punctures not very coarse and subcrenate, the suture and interstices with fine distant serial punctures, and more or less transversely rugose : the reflexed posterior dilatation on each assumes the form of two curves, the terminal one the larger. Underside shining, nigrescent, sparsely clothed with fine short greyish hairs. Prosternum usually somewhat convex and rather finely but closely punctate in front, nearly smooth, or with some transverse rugae behind the intercoxal suture. Metasternum more distinctly punctured near the sides than on the middle, the sides broadly impressed. Abdomen moderately finely, the 5th segment closelv, punctate. Female. — Rostrum more slender, very finely punctate, antennae inserted behind the middle, basal ventral segment simple. 3 . Length, 2| lines ; breadth, nearly | line. Whangarei and Hunua Range. Both sexes. 164 Transactiojis. Toura, gen. nov. Body fusiform-cylindric. Rostrum of nearly the same length, as thorax, nearly twice as long as that of 903. much more slender, evidently arcuate ; very slightly, just perceptibly, broader in front than behind ; a little dilated medially underneath ; nearly as stout but quite parallel in the female. Scrobes elongate. Scape somewhat curved, moderately incrassate apicallv, inserted distmctly before the middle, but only reaching the front of the eye. Funiculus rather elongate, 2nd joint nearly as long as the 1st, joints 3-5 somewhat laxly articulated. Club indistinctly annulate, moderate. Eyes rotundate, moderately prominent. The smooth occiput marked oft" in line with the back of the eyes. Thorax triangularly ovate, constricted in front. Scutellum distinct. Elytra slightly biarcuate at the base and rather broader than that of the thorax, subfusiform. Legs elongate and rather slender ; tibiae only a little expanded towards the extremity ; 3rd joint of the tarsi expanded and moderately bilobed. Prosternum elongate, intercoxal suture strongly curved. Basal 2 ventral segments as long as the metasternum. Rostrum bisulcate and tricarinate underneath. The nearly similar rostrum of both sexes, its upper curvature and unusual length, the antennal insertion, different scrobes, curved scape, slender legs, expanded and lobate 3rd tarsal joint, and more approximated front coxae are sufficient for generic separation of Wollaston's Pentarthrmn longirostre, which I adopt as the type of Toura. In the female the antenna? are im- planted before the middle, just the reverse of what is the case in Pentarthrum. It bears some resemblance to PhJceophagosoma. Toura longirostre, Wollaston. 904. Man. N.Z. Coleopt., p. 508. (Plate XV. fig- 5.) ... Nitid, piceous or nigro-piceous. legs and antennae pitchy-red. Rostrum rather finely and closely punctate, the interocular sculpture similar, the occiput smooth. Thorax rather abruptly contracted near the apex, finely punctured there; disc convex, moderately coarsely punctured, its sides moderately rounded. Elytra not perfectly parallel, slightly nar- rowed backwards : punctate-striate, sutural stride deep, the suture and interstices with fine serial punctures and slightly transversely rugose. Underside a little glossy, nigrescent, with some minute hairs, moderately coarsely punctate. Basal ventral segment broadly depressed, the terminal one with a large transverse oviform depression which is densely and minutely sculptured. 3 . Length, 2 lines ; breadth, nearly | line. Parua, Whangarei. Both sexes. T. fulva, Broun. 2188. Man. N.Z. Coleopt., p. 1243. Shining, fulvescent, club fuscous, tarsi yellowish. Smaller than 904. Rostrum very finely punctate. Thorax rather small, narrower than the elytra, more cylindrical, their sides very slightly and regularly rounded from the truncate base to the apical contraction, the disc more finely but less closely punctured. Elytra subparallel before the middle, gradually narrowed posteriorly, each slightly rounded at the base, their striae and punctures finer. ? . Length, If lines ; breadth, f line. Paparoa, near Howick. One. Broun. — Revision of the New Zealand Cossoiiidse. 165 T. morosa, Broun. 1749. Man. N.Z. Coleopt., p. 969. Rostrum rather longer than that of 904, slightly incrassate medially, the point of antennal insertion. Occiput not delimited in front. Thorax more curvedly narrowed near the base, its sides more strongly rounded. Humeral angles subrectangular. Nigrescent, each puncture with a minute greyish seta. Perhaps represents a distinct genus. Male incog. 2 . Length, 2^ lines ; breadth, | line. Howick (one). Mount Egmont (one). Both during 1884. Merisma, gen. nov. Subdepressed, elongate, minutely pubescent. Rostrum almost as long as thorax, evidently but gradually narrowed towards the middle, its frontal portion as broad as the head, the basal narrower ; in the female it is slender, parallel, and arched. Scrobes straight and elongate above, widened and nearly convergent underneath. Scape medially inserted, slightly curved, gradually thickened, barely attaining the front of the eye. Funiculus as long as the scape, 2nd joint nearly as long as the 1st, 3-5 subquadrate, each narrowed towards the base. Club rather narrow, oblong-oval, finely annulate, not much shorter than the funiculus. Eyes distant from the thorax and each other, only moderately prominent. The head, at each side, has two slight constrictions, the smaller immediately behind the eye ; the other, about equidistant from the eye and thorax, limits the smooth occiput from the sculptured part, which ex- tends nearly half-way from the eye to the thoracic margin. Thorax longer than broad, much narrowed and constricted in front, moderately rounded laterally. Scutellum distinct. Elytra slightly biarcuate at the base, which is rather broader than that of the thorax ; they are elongate and taper towards the extremity. Legs relatively rather short ; inner extreiuity of the tibi?e with a minute calcar ; 3rd tarsal joint moderately expanded, cleft nearly to its base, and consequently strongly bilobed. Underside plane. The rostrum with a central carina, which seems to project into the buccal cavity. Basal 2 ventral segments combined rather longer than the metasternum and broadly impressed, with their fine sinuous suture quite distinct, the 5th with a rounded depression occupying half of its area. Female. — Antennal insertion just behind the middle. The depressed elongated body, peculiar head and rostrum, strongly lobate penultimate tarsal joint, and much more approximated anterior coxfe amply justify the creation of Merisma for the reception of Wollaston's Pentarfhrum sharpianum. Merisma sharpiana, Wollaston. 926. (Plate XV, fig. 7.) Elytra rufescent, thorax and rostrum somewhat piceous, moderately shining. Rostrum slightly transversely convex, rather finely punctate in front, more closely and somewhat rugosely behind, the rather coarser punctuation of the head extending backwards for half the distance between the eyes and thorax ; there is usually a slight longitudinal impression on the vertex ; the occiput is not quite smooth, having some fine punctures, and being, like the rostrum and thorax, more or less densely and minutely sculptured. Thorax moderately closely and finely punctured, with a smooth median line. Elytra punctate-striate, the striae rather shallow, broad towards 166 Transactions. the extremity, suture and interstices with minute serial punctures, the 2nd from the suture somewhat elevated and abruptly bent outwards at the extremity. Underside dark rufous, shining, nearly glabrous, the slender pubescence most easily detected on the terminal ventral segment ; the punctuation no- where close, rather fine, slightly coarser on the prosternum. Metasternum with a short linear impression behind, not sulcate along the middle. Female. — Rostrum arched above, moderately slender. ^ . Length, 2| lines ; breadth, \ line. Tairua and Hunua Range. Wollaston's description I have not seen. M. aurantiaca, Broun. 2192. Man. N.Z. Coleopt., p. 1245. Fulvescent, slightly nitid, apparently calvous. Near 926 ; the rostrum not as broad ; scape rather more curvate ; the thorax, behind the middle, not broader than the base of the elytra ; scu- tellum transversal ; elytra less striate ; the tarsi shorter, their penultimate joint less expanded. 3 . Length, If lines ; breadth, | line. Tairua, Auckland. Unique. Tanysoma, gen. nov. Body slightly convex, narrow, subparallel, sparingly clothed with slender but distinct brassy hairs. Male. — Rostrum quite half the length of thorax, evidently but not abruptly narrowed behind the middle, stout, its frontal portion nearly as broad as the head. Scape inserted between the middle and apex, reaching the front of the eye, a little curved, its apical half subclavate. Funiculus rather laxly articulated, joints 2-4 narrowed towards the base, 5th sub- moniliform and transverse, 2nd longer than 3rd. Club oblong-oval. Head moderately narrowed anteriorly, but with a distinct sculptured plica or swelling which at each side extends just beyond the back of the eye. Eyes small, quite lateral, slightly prominent. Thorax triangularly ovate, con- stricted in front. Scutellum small. Elytra elongate, parallel as far as the hind thighs, slightly narrower than thorax. Legs rather elongate and slender; tarsi densely pilose underneath, their 3rd joint cleft almost to its base, with strongly developed and divergent lobes. Underside with short distinct yellowish hairs, moderately finely but distinctly punctured, the intervals densely and minutely sculptured. The prosternum elongate, the coxee much less separated than in Pentarthrum, with a distinct suture between them. Mesosternal suture well marked. Metasterniim shorter than the abdomen, medially sulcate. Basal 2 ventral segments broadly depressed medially, their suture sinuate and distinct. Female. — Rostrum more slender, on a lower level than the vertex, por- rect ; widest at the apex, gradually narrowed towards the middle, slightly dilated, at or just before the middle, where the antennae are placed, its basal half distinctly medially narrowed, almost abruptly contracted underneath. Head without any visible post-ocular plication. Metasternal groove ab- breviated. Abdominal depression shallow, the last 3 segments red, as in the other sex. Differs from Euophryum in being without any dilatation below the rostrum, in its longer scape being inserted nearer the apex, by the presence Broun. — Revision of the Neiv Zealand Cossonidae. 167 of the plica behind each eye, by the absence of any incrassation of the elytral margins, and by the well-developed and divergent lobes of the penultimate tarsal joint. Tanysoma angusta, Broun. 1626. Man. N.Z. Coleopt., p. 910. Subopaque, piceo-rufous, the funicle and tarsi paler. Rostrum quite opaque, with relatively coarse, close, shallow, rugose punctuation, which is continued to behind the eyes, the apical portion with fewer and much finer punctures ; the whole derm dull with dense minute sculpture ; the occiput finely punctate. Thorax evidently longer than broad, posterior angles curvedly narrowed, its sides only slightly rounded, gradually narrowed anteriorly and constricted near the apex ; disc slightly flattened, distinctly but not coarsely or closely punctured, more coarsely and rugosely near the frontal constriction. Elytra moderately punctate- striate, intermediate stripe shallow, interstices and suture with serial pvmc- tures and appearing rugose. Female. — Rostrum red, only slightly shining, its sculpture very much finer, the thorax with the linear median space nearly smooth. ^ . Length, 1| lines ; breadth, f line. Otago : Mount Maungatua and Dunedin. One pair. Stenotoura, gen. nov. Body subdepressed, very elongate and narrow, moderately shining, sparsely and minutely pubescent. Rostrum quite as long as thorax, arched above, slender, subparallel. 8cape inserted before the middle, elongate and slender, slightly thickened apically, flexuous, barely attaining the front of the eye. Funiculus elongate and slender, loosely articulated, 2nd joint longer than 3rd. Club ovate, elongate. Eyes not prominent, moderately distant. Occiput short, more or less distinctly marked off nearly midway between the eyes and thorax. Thorax triangular-ovate, only moderately constricted in front. Scutellum distinct. Elytra very elongate and parallel, narrowed posteriorly, nearly thrice the length of the thorax. Legs moderate, tibial hooks rather small ; 3rd articulation of the tarsi a little dilated, with short lobes. Toura differs in many details of structure. Agrilochilus may be at once distinguished by its opaque and densely pubescent surface. Stenotoura should be located between these genera. Stenotoura exilis, Broun. 2193. Man. N.Z. Coleopt., p. 1245. (Plate XV, fig. 6.) . • Nitid, dark red or ferruginous, antennae and tarsi paler. Rostrum very slightly, hardly perceptibly, narrowed behind, its punctu- ation moderately fine and close, somewhat longitudinally disposed, nearly smooth in front, a little convex but not at all carinate along the middle ; the vertex punctate to beyond the eyes ; the occiput with a few fine punc- tures. Thorax slightly wider behind the middle than elsewhere, basal margin a little incrassate ; disc unimpressed, distinctly but not closely punctured, more finely and closely in front. Elytra feebly striate but with distinct punctures, the intervals nearly as large as the punctures, interstices with indistinct distant serial punctures, closer along the suture. Underside flat, shining, ferruginous, minutely and scantily pubescent, finely yet distinctly and rather sparingly punctate. Anterior coxae dis- tinctly but not at all widely separated, little more than half as much 168 T ransarfions. as those of 903. Metasternum as long as tiie basal 2 segments, medially grooved behind, these 2 segments finely and remotely punctured, the in- tervening suture distinct and medially curved. Length, If lines ; breadth, ^ line. Tairua and Howick. One of each sex. S. lateritia, Broun. 924. Man. N.Z. Coleopt., p. 518. Shining, pale ferruginous, apparently glabrous. Near $ 2193, differing therefrom in having the scape more curvate, joints 3-5 of the funiculus more moniliform, disc of thorax slightly flattened, elytra less striate and the punctures on the interstices obsolete. ? . Length, \\ lines ; breadth, quite \ line. Tairua. Unique. S. prolixa, sp. nov. Subdepressed, very elongate and angustate, glabrous, slightly nitid, rufous, elytra paler. Rostrum longer than thorax, arched, slender, parallel, nearly smooth and shining near the middle, finely and distantly punctured in front, more distinctly behind and to beyond the back of the eyes, and minutely cori- aceous there. Scape medially inserted, flexuous ; 2nd joint of the funiculus e-\ddently longer than broad, 3-5 obconical, club oblong-oval, not annulate. Eyes slightly prominent. Thorax longer than broad, its sides gently rounded, a good deal narrowed anteriorly ; disc nearly plane, moderately finely but not c'osely punctured, intervals, especially near the sides, densely and minutely sculptured. Scutellum small. Elytra slightly bisinuate at the base, as wide as thorax there, subparallel or very gradually narrowed back- wards ; moderately finely striate-punctate, striate behind, interstices with minute serial punctures, and on some parts with minute irregular aciculate impressions, the sutural 2 striae on each rather deep near the apices. Legs rather short, the 2 hind pairs particularly. More elongated than S. exilis, the rostrum evidently longer, the an- tennal insertion a little further back, the derm more or less coriaceous instead of being smooth. 5 . Length, 1| lines ; breadth, nearly f Hne. Totara, Southland. A single female sent several years ago by Mr. A. Philpott, of Invercargill. Eutassa, gen. nov. i Body stout, subdepressed or only slightly convex, obviously pubescent. Rostrum a third shorter than the thorax, slightly arched in front, slightly narrowed behind the antennal insertion, before the middle, moderately stout. Scape moderately elongate, gradually incrassate, attaining the front of the eye. Funiculus as long as the scape, 2nd joint nearly as long as the basal one but more slender, 3-5 obconical, laxly articulated. Club oval, large, indistinctly annulate. Thorax constricted in front, up to that point quite oviform. Scutellum small but distinct. Elytra slightly narrowed posteriorly, the base slightly curved towards the scutellum, and as wide as the middle of the thorax. Legs rather elongate, the inner angle of the tibiae acutely mucronate, their hooks rather slender. Tarsi elongate, penultimate joint divided nearly to its base, the lobes elongate and divergent, the terminal with minute claws. Broun. — Revision of the New Zealand Cossonidte. 169 Female. — Rostrum of similar form, ratlier narrower and more finely sculptured. Underside shining, black, the terminal 3 segments rufescent ; pubescence brassy, fine but distinct ; evidently, but not coarsely or closely, punctate ; the sutures between the front and intermediate coxse straight, that between the basal 2 segments sinuate. Rostrum distinctly tricarinate. Metasternum and basal 2 segments of nearly equal length, the former medi- ally grooved behind, abdomen simple. The rostrum is as stout as that of Sericotrogus, but longer, narrowed posteriorly, and with the antennal insertion nearer the extremity. The head is shorter, and, like the eyes, more resembles Pentarthrum. Thorax broader, and constricted in front. The elytra are gradually attenuated posteriorly, instead of being narrowed towards the base, as in Sericotrogus, and the tarsal lobes are more elongate and divergent. Eutassa comatum, Broun. 1748. Man. N.Z. Coleopt., p. 968. Rostrum and thorax dark red and moderately shining, elytra somewhat fulvescent and glossy, legs and antennae infuscate red, the club and tarsi slightly paler ; the vestiture yellow, slender but conspicuous, legs finely pubescent, thoracic disc nearly bare. Rostrum and head distinctly and closely but not coarsely punctured, the former more finely in front. Thorax widest just behind the middle, well rounded ; disc obsoletely impressed behind, its punctuation not close, rather fine, closer and finer in front, apex nearly smooth. Elytra with some- what indefinite sculpture, subpunctate-striate near the suture, the punctures elsewhere seriate, interstices with serial punctures and rugulose, the 3rd slightly elevated behind, the apices singly rounded ; on each, between the shoulder and the middle, there is a broad shallow impression. J . Length, If lines ; breadth, quite f line. Howick. One pair only. E. fuscicollis, sp. nov- Subdepressed ; except the middle of the thorax, clothed with distinct yellow hairs ; thorax fuscous, elytra and rostrum slightly infuscate pitchy- red, antenn* and tarsi rufescent. Rostrum subopaque, distinctly, rugosely, and very closely punctured ; the punctuation continued to the slight swelling behind the eyes, pubescent there ; occiput curvedly narrowed anteriorly, very minutely and densely sculptured, and with a few fine punctures. Thorax longer than broad, its sides well rounded, a good deal narrowed and contracted in front ; disc unimpressed, its punctuation moderately fine, very scanty between the middle and each side, close and rugose at the sides, closer and finer near the smooth apical margin. Elytra elongate, subparallel to beyond the middle, narrowed posteriorly, the base slightly curved towards the scutellum, apices individually rounded, each slightly longitudinally impressed before the middle ; they are striate-punctate ; the suture and interstices have fine serial punctures and appear rugose, the 2nd from the suture thickened, somewhat elevated, and sharply bent outwards at the extremity. Underside with distinct and moderately close punctures and yellow pubescence, basal ventral segment broadly depressed, metasternum sulcate behind, rostrum tricarinate. More robust than E. comatum ; rostriim rather longer, broader, more densely sculptured, and subasperate ; the thoracic punctuation different ; antennae stouter and implanted nearer the middle. 170 Transactions. Ohs. — The individually rounded apices of the elytra should form part of the generic diagnosis, as it is a distinctive character amongst the Cos- sonidce. ^ . Length, 2| lines ; breadth, nearly ^ line. Waitakerei Range, Auckland. Unique. Adel, gen. nov. Body stout, moderately elongate, narrowed anteriorly, slightly convex ; clothed with numerous rather short and slender suberect setpe, similar to those on Entium aberrans. Rostrum quite half the length of thorax, not quite as broad as the head, slightly wider near the front than it is elsewhere, a little dilated at the point of antennal insertion, distinctly contracted near its base, moderately stout, and bearing erect setae in front and others horizontal along each side of the anterior half. Scrobes short, expanded towards the front of the eyes. Scape medially inserted, moderately elongate, very gradually thickened, attaining the back of the eye. Funiculus 5-articulate, 2nd joint but little shorter than the 1st, joints 3-5 subquadrate, all narrowed towards the base. Club oblong-oval. Head moderately globose, gradually narrowed anteriorly, the outline scarcely at all interriipted, the punctuation ceasing in line with the back of the eyes, which are flattened and nearly as far from the thorax as they are from each other. Thorax but little longer than broad, widest behind the middle, well rounded there, much narrowed and constricted in front, its base truncate. Elytra rather wider than the broadest part of the thorax, the base widely incurved towards the suture, only slightly curvedly narrowed near the extremity. Legs moderately stout, tibial hooks distinct, 3rd tarsal joint a little expanded, concave in front, with very short indefinite lobes. Prosternum deeply incurved in front, the coxae widely separated. Meso- sternal suture broadly curved between the coxae. Metasternum hardly as long as the basal 2 segments combined, slightly convex, feebly sulcate behind. Basal ventral segment not much longer than the 2nd, slightly transversely impressed behind, its frontal suture nearly truncate between the coxae, the 2nd with the fine frontal suture medially curved, the terminal rather short. The form of the head bears some resemblance to that of Agastegnus. The body is rather less convex than in Pentarthrum, and the hind-body is relatively broader throughout, whilst the rostrum and eyes are essentially different. It should be placed between Eutassa and Agastegnus. The scutellum is distinct. Adel crenatus, Broun. 1431. Man. N.Z. Coleopt., p. 804. Shining, dark red, antennae and tarsi paler. Rostrum finely, almost seriately, punctured, so as to appear slightly longitudinally rugose. Thorax broadly but not deeply impressed along the middle ; distinctly and evenly, but not closely, punctured ; the in- tervals smooth ; apical margin submetallic. Elytra with crenate-punctate striae, interstices with fine serial punctures. Underside shining piceous, minutely setigerous, the punctuation distinct, not close, and rather evenly distributed, the 2nd segment, however, more finely punctured. Length, If lines ; breadth, f line. Waitakerei Range. Unique. Broun. — Bexyision of the New Zealand Cossonida\ 171 Rhinanisus, Broun. Man. N.Z. Coleopt., p. 805. Subdepressed, moderately broad, finely pubescent. Rostrum more than half the length of thorax, contracted behind the middle in both sexes, broad in the male, cylindrical, but never slender in the female. Head rather broader in the male ; the nearly smooth occiput does not extend, even in the female, as far as the eyes, there being a punctate space behind these, which are only moderately prominent. Scape stout, rather short, gradually thickened, inserted just before the middle in both sexes, it attains the front of the eye. Funiculus 5-articulate, 2nd joint hardly longer than the 3rd. Club large, ovate, annulate near the extremity. Thorax triangularly ovate in the female, broader and more rounded near the base in the male, constricted near the front. Scutellum small. Elytra elongate, parallel, equalling the thorax in width, apical margins simple. Tarsi pubescent underneath, 3rd joint slightly dilated, excavate above and sublobate, the female less so. Underside plane, rostrum deeply grooved behind. The species composing this genus are only about half the bulk of Pentarthrum ; the antennal insertion, form of the rostrum, subdepressed body, and less widely separated coxa; distinguish them from that genus. Rhinanisus differs from Euofhryum in the much less prominent eyes, longer scape, simple elytral margins, more lobate 3rd tarsal joint, less robust body, and different rostrum. Rhinanisus fulvicornis, Broun. 912. Man. N.Z. Coleopt., p. 512. (Plate XV, fig. 9.) Shining, dark red, vertex piceous, antennae fulvescent ; pubescence scanty, fine, yellowish, and quite perceptible. Rostrum rather deeply incurved between the middle and base, the frontal portion almost as broad as the head, more finely and less closely punctured than the basal. Head closely and, in proportion to the small size of the insect, moderately coarsely punctured to behind the eyes ; this sculpture, in conjunction with the dark colour, render these organs indistinct ; occiput shining but not perfectly smooth, narrowed in front. Thorax longer than broad, widest and a good deal rounded near the base ; disc somewhat flattened but not impressed longitudinally, subfoveate near the middle of the base, moderately distinctly but not closely punctured. Elytra punctate-striate, the striae, however, not at all deep ; interstices with in- distinct serial punctures, and in some aspects appearing rugose. Female. — Rostrum slightly longer, narrower, more shining, and finely sculptured ; the thorax more gradually narrowed anteriorly. 3 . Length, 1 line ; breadth, nearly J line. Whangarei. One of each sex. "&"" R. parvicornis, Sharp. 913. Man. N.Z. Coleopt., p. 513. Subdepressed, moderately nitid, ferruginous, strongly punctate. Thorax slightly constricted. Elytra strongly striate-punctate, interstices fine y punctured, with very short indistinct setae. Rostrum opaque and thick in the male ; longer, more slender, and shining in the female. Length, 1 line. Auckland. 172 Transactions. R. contiguus, Broun. 923. Man. N.Z. Coleopt., p. 517. Near 912, J . Eostrum rather longer, more opaque, slightly longi- tudinally impressed between the antennae and base. Thorax, narrower, indistinctly impressed medially. S . Length, \\ lines ; breadth, \ line. Whangarei. Unique. R. sagax, Broun. 1750. Man. N.Z. Coleopt., p. 969. Nitid, castaneo-rufous, vertex darker. Club large. Thorax deeply constricted in front, broadly impressed along the middle. Elytra broader than thorax. Pubescence distinct yellowish. J . Length, \\ lines ; breadth, nearly f line. Mount Egmont. Unique. R. cheesemani, Broun. 2201. Man. N.Z. Coleopt., p. 1249. Shining, castaneo-rufous, pubescence extremely slender but rather elongate. Thorax not deeply impressed, frontal constriction deep. Rostrum slightly arched. Resembles the preceding, R. sagax. g . Length, IJ lines ; breadth, nearly | line. Mount Arthur. Both sexes. R. lewisi, Broun. Description being published at London. Elongate, rather slender, nitid, ferruginous, pubescence inconspicuous. Thorax distinctly medially depressed. Elytra plane, 3rd interstices dis- tinctly elevated and bent near apices. Paler than the j)i'eceding species ; base of elytra more or less infuscate. 3 . Length, IJ lines ; breadth, \ line. Broken River, Canterbury. Both sexes ; several specimens. R. elongatus, Broun. Description being published at London. Narrow and elongate, subopaque, piceo-rufous, antennae and tarsi rufo- testaceous, with minute greyish setae. Eyes not easily discernible, owing to the sculpture of the head. 5 . Length, If lines ; breadth, quite ^ line. Ashburton. One of each sex ; mutilated. R. subconvexus, Broun. Description being published at London. Nitid, rufous, pubescence scanty and slender. Rather smaller and paler than elongatus, less depressed than R. gracilis. Scape rather short. Thorax not closely punctate. Elytra slightly convex. 3 . Length, 1^ lines ; breadth, ^ line. Otara, Southland. Unique. R. suturalis, Broun. Description being published at London. Rufo-piceous, legs and antennae fusco-rufous. Elytra distinctly striate-punctate, the suture slightly elevated. Antennae rather elongate. Club narrow and somewhat flavescent. Length, 1;^ lines ; breadth, \ line. Totara, Southland. One. i Broux. — Revision of the Xew Zealand Cossoiiidfe. 173 R. confertus, Sharp. 2199. Man. N.Z. Coleopt., p. 1248. Narrow, siibdepressed, nigrescent ; tlie head, rostrum, antennae, and legs rufous ; shoulders fusco-rufous. Rostrum elongate, cylindric. Elytra deeply striate, the striae very closely punctured. Somewhat similar to R. parvicornis. I have not seen it. Length, 2| mm. Picton. R. constrictus, Sharp. 2200. Man. N.Z. Coleopt., p. 1249. Narrow, subdepressed, fulvo-rufous. Thorax longitudinally depressed on the middle, and with a slight smooth space on the middle. • Elytra flat, coarsely punctate-seriate, interstices impunctate. May be placed near R. parvicornis. I have not seen it. Length, 2;^3 mm. Grey mouth. R. sulcirostris, sp. nov. Elongate, subdepressed, dark rufous, elytra a little paler, club ful- vescent ; pubescence scanty, fine, and yellowish. Rostrum broad in front, distinctly narrowed behind the middle, the punctuation rather shallow but moderately coarse and rugose behind the middle, in front with some slender longitudinal rugae and some fine punc- tures ; a broad furrow extends from near the apex towards the forehead ; the coarse punctuation of the head is prolonged about half-way between the eyes and the thorax. Antennae stout ; 2nd joint of the funiculus very slightly longer than the 3rd ; club elongate-oval, rather narrow. Thorax moderately constricted in front ; if this portion were detached the remainder would be quite ovate ; disc subdepressed, moderately but not closely punctured. Elytra subparallel, the base slightly yet quite appreciably incurved medially, and about as broad there as the widest part of the thorax, behmd the middle ; they are distinctly striate-punctate ; near the suture, however, on each there are two striae ; interstitial punctures distant and indistinct. Tibiae with a slende'r mucro at the inner extremity. In some respects like R. contiguus. The rostal furrow, narrow club, and incurved elytral base, taken together, distinguish this species from all the others. J . Length, 1| lines ; breadth, J line. Mount Egmont. One, minus a leg. Camptoscapus, Broun. Ann. Mag. Nat. Hist., November, 1893. Subdepressed, with some minute greyish hairs. Rostrum more than half the length of thorax, moderately stout, very slightly arched, subparallel, or gradually narrowed towards the eyes in both sexes ; in the female rather more slender, with the antennal insertion behind the middle. Eyes moderately jjrominent, distinctly separated from the thorax by the short smooth occiput. Antennae moderately stout and elongate, inserted medially. Scape not at all short, incrassate but not abruptly clavate near the apex : this thick portion is bent backwards, the basal slightly in the opposite direction, in both sexes. Funiculus 5-articu- late, 2nd joint nearly as long as the basal, 3-5 transverse. Club ovate, 174 Transactions. finely annulate. Thorax triangular-ovate, constricted in front. Scutellum distinct. Elytra as wide as thorax, nearly parallel, gradually narrowed backwards. Legs moderately long and stout ; tibiae slightly expanded towards the extremity. Tarsi slender, penultimate joint hardlv at all dilated, excavate above but not lobate. In the Japanese Tychiodes the scape is short and flexuous, an uncommon character apparently, but it and its immediate allies differ from Ca)nptoscapus in other respects. From its New Zealand congeners it is readilv separated by the peculiar form of the scape. The eyes are comparatively large, and, though rotundate, extend much downwards. Camptoscapus sanguineus, Broun. Ann. Mag. Nat. Hist., November, 1893. Nitid, piceo-rufus, the vertex and elytra suffused with piceous ; pubes- cence scanty, slender, and cinereous, most easily seen on the posterior declivity. Rostrum slightly narrowed behind the middle, moderately finelv yet distinctly punctured, rather coarser behind, and abruptly terminating in line with the, back of the eyes. Thorax with obtusely rounded posterior angles, its sides moderately rounded and narrowed towards the frontal constriction ; disc almost flat, moderately finely, distinctly, but not closely punctured, more finely in front, the middle of apex smooth. Elytra at the base about the same width as the middle of thorax, subparallel, very gently narrowed posteriorly, their striae regular, moderately deeply and distinctly punctured, interstices with fine serial punctures. Tibiae but little dilated, not triangular, the front pair with yellow pubescence along the inner face and near the extremity ; claws very small. 3 . Length, quite IJ lines ; breadth, nearly f line. Mount Pirongia. Unique. C. planiusculus, Broun. 910. Man. N.Z. Coleopt., p. 511. Subdepressed, moderately shining, ferruginous, the fine short greyish hairs easily perceptible near the extremity of the rostrum and hind-body. Rostrum moderately distinctly punctured, longitudinally rugose, more finely and closely near the apex, the punctuation rather coarse on the vertex and continued to just beyond the back of the eyes, the constriction or frontal narrowing of the finely punctate occiput does not reach the eyes, which are moderately large. Club evidently pubescent, apparently triarticulate. Thorax longer than broad, distinctly rounded laterally, widest near the middle, abruptly narrowed near the front, closely and finely punctate there, but with the middle of the apex smooth ; dorsum subdepressed, distinctly but not closely punctured, more closely near the sides, the basal margin slightly thickened. Scutellum smooth. Elytra biarcuate at base, distinctly punctate-striate, interstices with serial punctures and rugulose, 3rd elevated and bent outwards at the extremity, femora slender near the base, clavate beyond. g . Length, If lines ; breadth, f line. Whangarei. One only. C. conicollis, Broun. 1306. Man. N.Z. Coleopt., p. 735. Elongate, subdepressed, dark red. Rostrum subparallel, shining, finely punctate ; occiput nearly smooth. Scape quite the length of funiculus. Thorax more triangular than 910 ; Broun. — Revision of the New Zealand Cossonidfe. 175 frontal constriction less deep and a little fnrther from the apex ; the disc rather more closely and distinctly pimctate. Elytral striae rather deeper, interstitial punctures more distinct. 2 . Length, if lines ; breadth, f line. Wellington. Unique. Macroscytalus, Broun. Man. N.Z. Coleopt., p. 736, Body rather broad, subdepressed, minutely and scantily pubescent. Rostrum more than half the length of thorax, moderately stout, narrowed behind the middle in both sexes. Occiput sharply limited at the sides close to the eyes ; the punctuation of the head ceases abruptly in line with these organs. Scape stout, medially inserted, subclavate near the extremity, it attains the front of the eye. Funiculus short, 2nd joint nearly as long as the short basal one, 3-5 compact, transverse. Club oblong-oval, acuminate, as long as or longer than the funiculus, distinctly pubescent. Eyes large, slightly prominent, subtruncate behind, widely separated. Thorax rather short and broad, its sides strongly rounded ; the moderate frontal constriction at each side extends obliquely towards the median discoidal linear impression. Scutellum small but distinct. Elytra rather short, subparallel or very slightly curved laterally, rather broader than the base of the thorax. Legs moderately stout ; hooks of the tibiae well de- veloped, inner extremity with a sharp calcar ; tarsi moderate, penultimate joint excavate but not lobed. This genus should follow Bhinanisus. The rather broad subdepressed Ijody and remarkably large antennal club, apart from other details, are characteristic. Macroscytalus laticollis, Broun. 1308. Man. N.Z. Coleopt., p. 737, (Plate XV, fig. 10 ) Body moderately shining, dark red, head and thorax somewhat piceous, club nigrescent. Rostrum for two-thirds of its length nearly as broad as the head, closely and finely punctured in front, more distinctly behind, and as far as the eyes, and with a linear impression from the middle backwards. There is a slender interocular fovea. Thorax hardly any longer than it is broad, impressed along the middle, most obviously near the base, and with 2 oblique frontal impressions, the surface moderately closely and rather finely punctured. Elytra with indistinctly curvate sides, punctate-striate, interstices with numerous distinct serial punctures. Underside plane. Mesosternum not abbreviated. Basal 2 ventral seg- ments broadly impressed, and equalling the metasternum in . length ; the latter finely grooved. Coxae small, widely separated. S . Length, IJ lines ; breadth, f line. Parua, Whangarei. One of each sex. M. depressus, Broun. 1433. Man. N.Z. Coleopt., p. 807. Shining, castaneo-rufous, the interocular area, front of thorax, and the club somewhat piceous. Rostrum finely punctured and shining. Interocular fovea small. Thorax with a shallow median impression at the base only. Elytra broadly im- pressed before the middle. Club much longer than the funiculus. S . Length, 1| lines ; breadth, j line. Parua. Unique. 176 Transactions. M. russulus, Broun. 1309. Man. N.Z. Coleopt., p. 737. Castaneo-rufous, shining, antennpo slender, club pale fuscous. Rostrum subcylindric, slightly narrowed behind, finely punctate and shining. Interocular fovea very distinct. Apex of thorax shining, but finely punctured, disc not flattened, with a small basal impression. Elytra very slightly rounded, unimpressed, rather broad. ? . Length, 1| lines ; breadth, f line. Tairua. Unique. M. remotus, Sharp. 914. Man. N.Z. Coleopt., p. 513. Rufo-piceous, club nigrescent. Thorax medially impressed near the base. Interocular fovea indistinct. (^ . Length, I| fines; breadth, quite j line. Tairua. One pair. M. frontaUs, Broun. Ann. Mag. Nat. Hist., November, 1893. Shining, rostrum and thorax rufous, elytra and legs rufo - castaneous, club dull black. Thorax shining and only feebly constricted in front. Literocular fovea indistinct. Elytra indefinitely impressed before the middle. ? . Length, 1| lines ; breadth, nearly | line. Hunua Range. One. M. badius, Broun. 920. Man. N.Z. Coleopt., p. 516. Broad, testaceous or slightly infuscate. Thorax short and broad, unimpressed, abruptly narrowed in front. 3 . Length, \\ lines ; breadth, nearly f line. Whangarei. One pair. M. crenatus, sp. nov. Subdepressed, moderately nitid, rufo-piceous, the frontal half of rostrum and the humeral area rufescent, antennae clear red and shining, club nigrescent and densely pubescent. Rostrum evidently narrowed behind the point of antennal insertion, before the middle, broadly sulcate from thence to the back of the eyes, distinctly yet finely punctate, more finely and distantly in front ; occiput nearly smooth and shining. Thorax hardly longer than broad, considerably narrowed and constricted in front, widest behind the middle, strongly curvate there, the basal margin minutely prominent at the sides ; disc flat, with a more or less evident smooth median line reaching the constriction but distant from the base, its punctuation moderately fine and close. Elytra rather wider than thorax at the base, very gradually narrowed posteriorly, moderately crenate-striate, interstices with fine serial punctures, and some- what rugose. Legs closely punctured, 3rd tarsal joint a little expanded but not lobate. Pubescence scanty, greyish, visible only on the posterior part of the elytra. Female. — Rostrum more slender, shining, finely and sparingly punctured, distinctly narrowed behind the middle. The rostral canal and crenate-punctate elytral striae will enable this species to ))e recognised. 1308 and 914 most nearly resemble it. 3 . Length, If lines ; breadth, | line. Hunua Range and Woodhill. One at each. Broun. — Revision uj the yew Zealand Cossonidse. 177 Baeorhopalus, Broun. Man. N.Z. Coleopt., p. 806. Subdepressed, rather broad, almost elongate-oval, glossy, glabrous. Female. — Rostrum moderately arched, shorter than thorax, stout but not broad, slightly dilated medially, the point of antennal insertion mode- rately narrowed near the base. Head globose underneath, not elongated, gradually curvedly narrowed to the same width as the rostrum, the outline not interrupted by any prominence of the eyes, which are rather small and nearly flat ; the occiput not distinctly marked off from the eyes or vertex. Scape stout, much thickened near the extremity, medially in- serted, and attaining the front of the eye. Funiculus compactly articulated, 2nd joint not perceptibly longer than 3rd. Club oblong-oval. Thorax strongly rounded laterally, constricted in front. Scutellum distinct. Elytra indistinctly curved at the sides, gradually narrowed behind, their base a little wider than that of the thorax. Legs moderate, 3rd tarsal joint not lobate. , Male. — Underside glabrous, nearly plane, shining, castaneo - rufous, very finely and distantly punctured. Basal 2 ventral segments as long as the raetasternum, broadly depressed along the middle, the metasternum grooved behind, prosternum quite truncate in front. The mesosternal suture and that between the basal 2 segments fine and nearly straight, 5th segment with a small impression at each side. The natural position of this genus is, without doubt, next to Macro- sci/talus, which, though similar in form, is distinguished by the altogether different head, less slender rostrum, larger and more prominent eyes, larger club, &c. The coxse are less widely separated than in Pentarthrum. Unfortunately, this and three or four closely alUed genera are seldom met with ; all their species are rare. Baeorhopalus glabrus, Broun. 1305. Man. N.Z. Coleopt., p. 735. Glossy, rufous, elytra chestnut-red. Rostrum with fine almost seriate punctures, the interocular sculpture nearly similar, with a slender fovea. Thorax nearly flat, as broad as it is long, widest just behind the middle, its sides strongly rounded, narrowed towards the constriction, very finely and distantly punctured, with a slight impression before the scutellum. Elytra rather flat, finely punctate-striate, interstices moderately broad, with fine serial punctures. The male specimen is mounted on its back. 2 , Length, If lines ; breadth, | line. Parua, Whangarei. Two examples. Selocomis, gen. nov. Subdepressed, subfusiform, rather thickly clothed with decumbent con- spicuous yellow hairs. Rostrum nearly the length of the thorax, quite half the width of the head, sUghtly narrowed near the base, not marked oil from the forehead, abruptly truncate or shaved oft' at its apex. Scrobes obhque. Scape in- serted behind the middle, attaining the centre of the eye, elongate, gradually incrassate. Funiculus laxly articulated, rather short, 2nd joint distinctly longer than 3rd, joints 3-5 transverse, 5th almost cup-shaped. Club com- pact, opaque, densely pubescent, very elongate, fully the length of the whole funiculus. Head short, narrowed anteriorly, globose underneath, the occiput short. Eyes subdepressed in front, slightly prominent behind, 178 Transactions. large, transversal. Thorax but little longer than broad, widest behind the middle, well rounded there, curvedly narrowed towards the abrupt frontal contraction. Scutellum distinct. Elytra rather broader than the thorax, parallel to beyond the hind thighs, curvedly narrowed behind, slightlv transversely bi-impressed above. Legs stout, only moderately elongate ; tibise uncinate, and acute at the inner extremity. Tarsi moderately narrow, 3rd joint slightly dilated, concave in front, entire below, not lobate. Coxaj widely separated. Rostrum, underneath, wdth two sharply defined grooves, and therefore appearing tricarinate. Metasternum rather longer than the basal 2 ventral segments taken together, distinctly medially sul- cate. Mesosternal suture straight. Basal 2 segments slightly convex, their suture distinct and a httle sinuate, the 1st transversely impressed behind. Underside glossy, piceous, the last 3 abdominal segments rufescent, with distinct rather evenly distributed punctures, almost quite glabrous, having only a few minute hairs on the terminal segment, and therefore in marked contrast to the upper surface. Exactly intermediate between Macroscytalus and Agastegnus, having the disproportionally long club of the former and the facies of the latter, from which, nevertheless, it differs in having shorter and thicker legs, more prominent eyes, stouter and differently inserted antennae, different rostrum. &c. From Macroscytalus it is readily distinguishable by a glance at its conspicuous vestiture. Selocomis seneopiceus, Broun. 915. Man. N.Z. Coleopt., p. 513. Fusco-rufous, sUghtly bronzed ; femora piceous ; rostrum, antennae, and tarsi rufous ; shghtly shining. Rostrum parallel for more than half of its length, moderately closely and finely punctured, more distantly and finely in front. Head pilose, distinctly but not closely punctured. Thorax broadly impressed medially, with a slightly raised smooth central line, distinctly but not closely punc- tured, the apical margin nearly smooth. Elytra slightly broadly impressed before and behind the middle, their striae somewhat indefinite, but with the punctures on the suture and interstices unusually close and distinct, the 3rd thickened, elevated, and bent at the extremity, and causing an apparent depression beyond each of them. Length. If lines ; breadth, nearly | line. Mount Manaia, Whangarei. One only. Glyphoramphus, Broun. Man. N.Z. Coleopt., p. 970. Body subdepressed, sparingly clothed with slender yellow hairs. Rostrum shorter than the thorax, not quite as broad as the head, just perceptibly medially incurved, quite vertical in front, deeply concave between the antennae. Head moderately globose ; occiput short, slightly narrowed in front. Eyes moderately large and prominent, rotundate, widely sepa- rated. Scape inserted near the apex, attaining the eye, slightly flexuous. moderately elongate, slender near the base, subclavate for half its length. Funiculus rather slender, 2nd joint nearly as long as but more slender than the 1st, joints 3-5 laxly articulated, 5th very short. Club nearly oblong- oval, large, indistinctly annulate. Thorax about as broad as it is long, its sides strongly rounded, base truncate, deeply constricted in front. Scu- tellum distinct but small. Elytra subparallel, gradually narrowed behind, apices slightly rounded singly, the base evidently broader than that of the Broux. — Revision of the New Zealand CossonidiX". 179 thorax. Legs stout and elongate ; femora swollen and obtusely angulate below ; tibise moderately and gradually expanded, their hooks rather small but quite distinct, with a slender spiniform process at the inner extremity. Tarsi moderately narrow, terminal joint as long as the basal 3 combined, 3rd moderately expanded and subbilobed, claws small. The form most nearly resembles that of Baorhopalus, the thorax par- ticularly. The rostrum is thick vertically, and the scape unusually in- crassate towards the extremity. There is no approximate genus amongst the Pentarthrides. Glyphoramphus rarus, Broun. 1735. Man. N.Z. Coleopt., p. 971. Nitid, piceo-rufous tinged with castaneous, antenna^ pale ferruginous. Head and rostrum densely and very minutely sculptured ; the punctures on the head are rather fine, but not close, and gradually become finer and fewer towards the front of the rostrum. Thorax distinctly longitudinally impressed, moderately finely and not closely punctate, the apex raised and nearly smooth. Elytra slightly broadly impressed before and behind the middle, regularly and moderately finely striate-punctate, striate behind : interstices finely seriate punctate and rugose, the 3rd and the suture elevated and sharply bent at the extremity. 3 . Length, IJ lines ; breadth, f line. Mount Egmont. Unique. Belka, gen. nov. Body fusiform, moderately convex, evidently clothed with decumbent elongate yellow pubescence. Rostrum rather shorter than thorax, subparallel, slightly narrowed near the base, cylindric, half the width of the head, and bearing many fine but elongate setae along its sides ; these are most easily seen from underneath. Scrobes prolonged to the inner and lower part of the eyes, their upper margins sharply defined there. Scape inserted behind the middle, attaining the centre of the eye, elongate, only moderately slender. Funiculus rather stouter than the scape, 2nd joint longer than 3rd, joints 3-5 become shorter. Club ovate. Head rather short, occiput strongly globose underneath, slightly narrowed but not perceptibly marked off in front. Eyes slightly prominent, moderately small, almost transversely oval. Thorax longer than broad, widest behind the middle, well rounded there, a good deal narrowed and constricted in front. Scutellum small. Elytra broader than thorax at the base, subparallel, narrowed behind, base slightly biarcuate, apices not distinctly rounded separately. Legs stout, femora subclavate ; tibipe uncinate ; penultimate tarsal joint slightly dilated, concave above, entire below, terminal rather thick, with small claws. It would be absurd to leave the type of this genus with Pentarthrum. The rostrum is like that of the female Pentarthnim^ (903) in length, but is slightly stouter, and quite perceptibly narrowed near the base. The eyes are distinctly smaller and more transversal. The scutellum is smaller. The scape cannot reach the back of the eye. The metasternum is. shorter, ^^ ith a very short groove behind. The basal 2 ventral segments are unim- pressed, but their suture is well marked and sinuate. The rostrum under- neath has 2 sharply impressed grooves. The more robust body and legs, different antennal insertion, and entirely dift'erent vestiture, &c.. distinguish it from Attarus, near which it should be placed. 1 80 Transa c tions . Female. — Rostrum rather longer, but not appreciably more slender. Thorax different, widest near the base, gradually narrowed from that point ; posterior angles quite oblique. Apt to be mistaken for a distinct species. Belka spadicea, Broun. 1628. Man. N.Z. Coleopt., p. 911. Subopaque, rostrum and elytra slightly nitid, fusco-castaneous, legs of a chocolate colour, antennae and tarsi piceo-rufous, pubescence more abundant on the elytra than on the thorax. In the male the elytra are somewhat rufescent. Rostrum moderately finely and not closely punctured throughout. Head pubescent, moderately punctate ; occiput not quite smooth. Scape glabrous, the funiculus finely and sparingly setose. Club densely and finely pubescent, slightly annulate. Thorax with a smooth median line, mode- rately finely and not closely punctured, disc convex, frontal constriction deep. Elytra as broad as the widest part of thorax, their striie rather shallow, crenate-punctate, the punctuation becoming indistinct behind, interstices rugose and seriate-punctate. Underside rufo-piceous, slightly nitid, the whole derm densely and minutely sculptured, the setae greyish and slender but numerous, the punctuation moderately coarse but not close. cT . Length, If lines ; breadth, f line. Dunedin. One of each sex. Attarus, gen. nov. Elongate, fusiform-cylindric, slightly transversely convex, a little shining, sparingly clothed with slender but quite perceptible pubescence. Rostrum porrect, a little arched in front, rather shorter than thorax, slightly narrowed behind, in front more than half the width of the head. Scrobes linear, directed obliquely towards the lower and inner part of the eyes. Scape elongate, only moderately stout, inserted at or before the middle, and attaining the front of the eye. Funiculus elongate, basal joint large, 2nd not distinctly longer than 3rd, 4th and 5th short. Club ovate, stout, not articulated. Head rather short, moderately globose, the occiput curvedly narrowed towards the eyes, but not constricted or marked off in front. Eyes rotundate, only slightly prominent, lateral. Thorax longer than broad, widest behind the middle, well rounded there, a good deal narrowed and constricted near the front, base truncate. Scutellum minute. Elytra subtruncate at the base, as broad as the widest part of the thorax, gradually narrowed posteriorly, their apices individually rounded. Legs relatively rather slender ; tibiae straight and hardly at all expanded, uncinate ; tarsi stout, the terminal joint quite the length of the basal 3 united, 3rd a little expanded, widely concave in front, not distinctly lobate, apparently entire underneath. Prosternum incurved in front, the coxae more approximated than in Pentarthnim. The metasternum elongate, nearly as long as the abdomen, finely medially sulcate, 2nd ventral segment shorter than 1st, their suture distinct and undulate. The structure of the antennae and tarsi, irrespective of other charac- teristics, is enough to prevent the association of the type of this genus with Eucossonus. It cannot be referred to Agastegnus, which is composed of depressed, long-legged insects. Sericotrogus has an entirely different head. &c., and the other Pentarthrum allies also exhibit disparities. i Broun. — Revision of the New Zealand Cossonidse. 181 Attarus tristis, sp. nov. Angustate, dark piceo-rufous, legs rather lighter, antennae fulvescent ; slightly nitid, pubescence greyish-yellow. Eostrum shining, rufescent, distantly and finely punctured in front, nearly smooth along the middle, the punctuation becoming coarse, somewhat elongate and rugose on the vertex ; the occiput also with some distant punctures. Eyes much less prominent than in Pentarthrum. Thorax un- impressed ; very coarsely, closely, and rugosely punctured at the sides ; the disc less coarsely and closely, on the middle especially, more closely in front ; the apical margin, however, is smooth, and of a somewhat metallic reddish-coppery hue. Elytra a good deal narrowed at the posterior declivity, the apical margins rufescent and evidently rounded singly ; they are regu- larly and distinctly but not coarsely striate-punctate, quite striate behind, the suture and interstices finely seriate-punctate and slightly rugose. Legs with minute yellowish setse, most conspicuous along the inner face of the front tibiae. Length, If lines ; breadth, f line. Paparoa, Howack. Unique. A. castus, Broun. 1307. Man. N.Z. Coleopt., p. 736. This species must be detached from Pentarthrum. The rostrum is rather longer than that of A. tristis, similarly sculptured and narrowed behind, but along each side it bears several slender outstanding yet not very elongate setae. Occiput smoother and more convex, and therefore more distinctly marked oft" from the close interocular punctuation. Disc of thorax very slightly and indistinctly flattened ; the slender yellow hairs on its sides are quite easily seen. Scutellum small and seemingly bent downwards in front, instead of being horizontal. Elytra with more distinct and closer interstitial punctures ; those in the striae are more quadrate, and are sepa- rated by short intervals only ; the yellow hairs are more numerous. Length, IJ lines ; breadth, | line. Whangarei. One. '^b^ A. vestitus, Broun. 916. Man. N.Z. Coleopt., p. 514. Body dark piceo - rufous, tarsi and antennae red, club fulvescent ; pubescence distinct, yellow, rather elongate and slender. Rostrum rather broad, incurved behind the middle ; rather coarsely, relatively, punctured and longitudinally rugose, the punctures not as close on the head ; the occiput also wath a few punctures. Thorax with the median line smooth, coarsely and rugosely punctured, more closely at the sides than on the disc, very closely near the smooth coppery front margin. Elytra subpunctate-striate, quite striate behind and at the base ; the suture and interstices finely seriately punctate and slightly rugose. Underside shining, rufo-piceous, with minute setae along the middle of the breast, but on the abdomen and along the sides the setae are more elongate and obvious ; the punctuation on the sides, the front of the pro- sternum, and on the basal 2 ventral segments is coarser than alone: the middle of the sternum ; base of presternum transversely rugose and punctate. Prosternum truncate in front. Rostrum medially grooved underneath, the groove with sharply defined borders. Buccal cavity large. Meta- sternum elongate, rather shorter than the abdomen, medially sulcate. Basal 182 Tranmction^. ventral segment broadly impressed, 2nd shorter, their suture undulate, the 5th with elongate pubescence. The rostrum is broader, the eyes more prominent, and the antennae shorter and stouter than in the preceding two species. The scutellum is sunken, and does not seem to penetrate between the elytra. The description is given in detail in case the discovery of more specimens should make it expedient to treat this species as the representative of a distinct genus. There can be no doubt as to its being a male. vv / ^ / W N.Z. born population of N.Z. ... ; p^f^^^j^^ ._ ' vS«^ VN. 1 ^ \ Number of lunatics per lo.ooo of population c ^j^ip """"'" ^^~ \ \ "■ ~ -*1 '-^■^ ^^o><^-- — ^ \ \> T*'' 1 ^-- ^V ^ ■! ^" ^-^- -" X ^\v ^^ -*•"". ^"^ -> i^_ ^^^-Os^ , ;_._ .^..-=f<=-' '' ' 50 40 30 20 TZ^- 10 0-5 5-10 10-15 15-20 20-25 25-30 30-35 35-40 40-45 45-50 50-55 55-60 60-65 G5-70 70-75 75-80 SOanJover.. Age periods. To illustrate the extent of this peculiarity that has to be allowed for, let us compare the age-periods 20-25 and 45-50. The number of lunatics per 10,000 in the later period is more than six times as great as it is in the earlier. Our total population in the later period is about two-fifths of that in the earlier, whereas our immigrant population of the later period is almost double that of the earlier. Further, whereas in the period 20-25 our immigrant population only constitutes one-sixth of the whole population of that age-period, in the later age-periods it practically constitutes the whole population of the periods. We have further to take into account the very considerable excess of males in our immigrant population, amounting to nearly 50 per cent., and their greater rate of insanity, and also the excess of females in older countries. In fig. 2 we have the graphs representing the population of New Zealand not New-Zealand-born. The excess of males stands out clearly, and a comparison of these graphs with those in fig. 1 for the whole population reveals clearly to the eye the exceptional character 8— Trims. 2 -20 Transactions. of the age-distribution of those not born in New Zealand. The graphs representing the rates of lunacy for the two sexes are also repeated in fig. 2, and two other graphs are given representing how our population above twenty years of age and not New-Zealand-born would be distributed in age and sex if such distribution were the same as that of the population of England and Wales as given in the census of 1901 ; or, in other words, representing the age and sex distribution of a portion of the population of England and Wales over twenty equal in number to that of our population over twenty not New-Zealand-born. A comparison of these graphs with Fig. 2. Population not N,Z. born The same over twenty years of age dis- tributed in age and sex as in census of England and Wales. 1901 I Males i t Females - Number of lunatics per 10. o'"© of population _ 'Males _ — — . Males _._. ■ , y"] T^ 20 lu 20 10 0-5 5-10 10-15 15-20 20-25 25-30 30-35 35-40 40-45 45-50 50-55 55-60 60-65 65-70 70-75 75-30 80 and over. - Age periods. the others in the same figure again reveals clearly the exceptional character of the age and sex distribution in question. It is obvious, then, that, in view of the very different rates of insanity prevalent in the various age- periods, the figures as presented by Dr. Hay cannot be accepted as any indication of the comparative insanity of the immigrant and his country- men at home. In Table II I have made an endeavour to roughly measure the correction that must be applied to allow for the features I have pointed out. The first column gives the age-periods beginning at 20-25, the next two give the population of New Zealand according to age-period and sex, and the next two again our immigrant population classified in the same way. The sixth and seventh columns give our total immigrant population above the age of twenty redistributed in respect to both age and sex proportionally to the population of England and Wales according to the census of 1901. The next two columns again give the New Zealand rates of lunacy, which have been already shown to apply generally to the New-Zealand-born and the immigrants as a whole. The last two columns give the number of immigrant lunatics there would be if our immigrant population of twenty years and over were distributed in age and sex as the population of England and Wales is distributed. Segar. — Insanity: Some Gomparative Statistics. 227 Table II. Population. Not New-Zealand-bc ■ ru. Number of Lunatics per 10,000. Number of Lunatics in Actual. Distributed. Distributed Population. Ages. Males. Females. m a "3 QQ "3 a A/'alcs, 1901 jFemales Number of lunatics per 10.000 of population '"*'«« ( Females > \A k. \ \ \ . [ Ki ^ ^N i ^ > ^>.- =tsn •=4 1 ,.- .•^* —•'"^ >'' --- ^ ^ ^ .](! in 1 .'■ 1 ^ ■>rl •H\ ■>^ 0-, Qn Qn o^ <■ >- __l 40 30 : 20 10 5 Ag. P.nods. ' ■'"'" ■'^''"' •^•'"^" ^'^■^'■' ^-^-^O ^°-^^ 55-GO G0-6u G5-70. 70-75 75-80 80 and over. ofj[age there should have been returned at the various age-periods in the census of 1906 if our population over twenty had been distributed in age and sex as was that of England and Wales at the census of 1901. Table IV. ■ Population of The Same Lunatics per 10,000 of Population. Number of Age-periods. New Zealand. redistributed. Lunatics. Males. Females. Males. Females. Males. Females. Males. Females. 20-25 49 , 370 45,238 40,947 45 , 831 15-39 11-05 63 51 25-30 49,308 43,140 36,933 41,603 25-74 22-95 95 95 30-35 37,798 32,621 32,190 35,415 41-80 33-72 135 119 35-40 32,329 27,794 28,763 30,889 60-32 48-93 173 151 40-45 24,451 20,930 24,954 26,502 75-66 63-54 189 168 45-50 21,424 17,003 21,131 22,613 86-35 92-92 183 210 50-55 18,336 13,563 17,690 19,262 105-26 103 96 186 200 55-60 13,984 10,958 13,812 15,434 120-85 114-07 167 176 60-65 12,452 9,442 11,412 13,847 145-36 105-91 106 142 65-70 11,524 7,599 7,854 9,656 138-84 125 02 108 121 70-75 7,567 4,616 5,4.35 6,976 11101 106-15 60 74 75-80 3,698 2,373 3,144 4,210 127-10 92-71 40 39 80 and over 1,865 1,546 1,949 2,979 126-60 97-02 25 29 Total 284 , 106 236,823 246,212 274,717 1,590 1,575 520 ,929 520 929 3,] 165 230 Transactions. The result of this calculation is to give 3,165 lunatics of specified ages of twenty years and over, of which 1,590 would have been males and 1,575 females — that is, the two sexes would have been almost exactly equal in numbers. The number of such actually returned at the census of 1906 was 3,026, of which 1,793 were males and 1,233 females. Instead, then, of the number of the female lunatics being 0-61 of that of the males, it would have been 0-99, a relative increase of 62 per cent. It must further be borne in mind here, as elsewhere, that the dealing with quinquennial age-periods does not make by any means a complete correction, which would undoubt- edly give an actual excess of female lunatics. The result we have obtained does not. however, explain the whole of the apparent difference between this country and England and Wales, for in the latter there is returned a substantial excess of female lunatics, the numbers recorded in the census of 1901 being — Lunatics. Imbecile and Feeble-minded. Total. Males . . . . . . 37,583 24,480 62.063 Females .. .. 46,189 24,402 70,591 But the allowanceSjWe have made make the contrast very much less marked, and bring it more within the uncertainties of such international statistics. The difference remaining unaccounted-for affords a rather unsafe foundation for argument and speculation. In conclusion, we may consider briefly how the female really stands with respect to the male in New Zealand in the matter of liability to insanity. At the census of 1906 there were returned, at specified ages of twenty years and over, 1,793 male and 1,233 female lunatics. I shall not trouble the reader with another table ; but if, in the manner of previous tables, we allow for the difference in numbers and in age-distribution of the sexes by supposing there had been a female population equal in numbers and similar in age- distribution to the male population, but retaining the female lunacy-rate at the various ages, we find that there would have been 1,567 instead of only 1,233 female lunatics. The comparison of this number 1,567 with 1,793, the actual number of male lunatics, is the best way of comparing briefly the liability of the two sexes to lunacy, since in it both the inequality in the numbers of the sexes and the dissimilarity in their age-distributions are allowed for. It is interestins further to notice the influence of alcoholism. In 1906 there were admitted to the mental hospitals of this country 401 males and 277 females. Amongst these cases seventy-three of the former but only eleven of the latter were attributed to alcoholism. In 1907, again, the numbers of admissions were 421 males and 279 females. Of these cases, seventy-one of the former but only eleven of the latter were attributed to alcoholism. In the two years the excess of male over female cases due to alcoholism is greater than one-seventh of the total number of male cases. Unless the proportion of recoveries is much greater for this class of patient than for those that owe their insanity to other causes, these numbers would indicate that the differ- ence remaining between the insanity of the males and females in New Zealand that has not already been accounted for by the differences in numbers and age-distribution is entirely explained by the greater excessive indulgence of the male sex in alcohol, and the ravages this indulgence makes on the sanity of the sex. Best. — Maori Forest Lore. 231 Art. XXXII. — Maori Forest Lore : Being some Account of Native Forest Lore and Woodcraft, as also of many Myths, Rites, Customs, and Super- stitions connected with the Flora and Fauna of the Tuhoe or Ure-wera District. — Part II. By Elsdon Best. [^Read before the Auckland Institute, 18?A November, 1908.] Harakeke {Phormium tenax). The harakeke, or flax, as it is commonly termed, has never obtained to any great extent in Tuhoeland, on account of its being essentially a forest district. Only the inferior varieties of flax were here found growing, and the better varieties were only obtained by means of cultivation. The varieties which produce the better grades of fibre are alluded to as whitau (sometimes hitau), while those which contain poor, weak, non-durable fibre are termed harakeke maori, or common harakeke. The following are the names of the varieties of flax known to the Tuhoe Tribe, which people seem to have imported some of the better varieties from the Waikato, for purposes of cultivation, about six generations ago : — 1. Oue. — This variety produces the best fibre, much prized in former times for the manufacture of the better class of garments. It was not indigenous to Tuhoeland, but was cultivated. 2. Pari-taniwha. — Produces a good fibre, which, however, requires to be steeped in water when scutched, or it assumes a reddish colour. After being soaked a while it is taken from the water and hung up to dry and bleach. 3. Wharariki. — Sleeping-mats and such things are made from the green, unscutched leaf. i. Bataroa. — Produces a fibre of medium quality. 5. Ngutu-nui. — Nets and snares are made from the leaf of this variety. 6. Huhi. — An inferior variety. Grows in swamps. 7. Tutae-manu. — An inferior fibre. 8. Awanga (or Aoanga). — Variegated variety. 9. Taneawai. 10. Ruatapu. — Formerly looked upon as being tapu, as its leaves, or fibre, were used in dressing the hair of chiefs. 11. Tukura. — A swamp-growing variety. The rataroa variety is also known as motu-o-ruhi. Shortland speaks of rongotainui, motuorui, and mangaeka as being the names of varieties of flax {Phormium). The latter name is applied by the Tuhoe people to the brownish-yellow strips of flax-leaf inserted in certain Native garments, and which colour is produced by exposing the strips to the heat of a fire. Such a garment is also termed a mangaeka. Shortland, however, speaks of the word harakeke as though it were a specific term for a single variety of flax, whereas it is essentially a generic term, embracing all varieties. The atvanga variety is used in making baskets and mats. Colenso gives tamure as another name of this variegated variety. Te rau o Papoua is said to be a term applied to growing flax, while te rau o Huna describes the fibre 232 Transactions. when scutched and prepared for use. Hence the former term is applied to a rough cape {for a), and the latter to a fine garment of dressed fibre. Local Natives say that an edible variety of flax formerly grew at Tieke. in the Rua-tahuna district. The leaves were dark-coloured, with reddish edges. The base of the leaves was eaten. This plant has disappeared. In this connection, I take the following from a newspaper item : " Mr. McGregor said that there is an edible variety of flax in the Taupo district. It is called kopakipaki-ika by the Natives. The main root grows to a great length. It is white in colour, and resembles celery outwardly. It has a sweet taste, which is a contrast to the bitter taste of the ordinary flax." Natives profess to know two sexes of the oue variety of flax. They state that the leaves of the male plant are more pointed than those of the female plant. The latter leaves are shorter, and do not give so long a fibre. The edges of leaves of the female plant are a light-reddish colour {puwhero). Leaves of the male plant have reddish streaks, called kakaka, in them, as you see light-coloured streaks in a leaf of toi {Cordyline indivisa). The fibre produced by the female plant is white and soft, that of the male is somewhat harsh and has a reddish tinge {ma pmvhero). The Natives, in former times, often planted the commoner varieties of flax near their dwellings, as the leaves were much used in the manufacture of small baskets to hold cooked food, which baskets were used but once. The varieties producing better fibre were planted usually at the edges of cultivation-grounds. A plant would be divided and the fans planted out in the fourth month of the Maori year — i.e., in the spring. It was considered necessary to put two plants in each whawhama or hole dug for the purpose. It was unlucky to plant an odd number {Mchemea ka kehe, he aitua) — the plants would not flourish. Such a flax-plantation is termed a pa fiarakeke. The ground around the plants was kept clear of weeds. Any old leaves were cut away so as to promote a more vigorous growth in the plant ; also, if the young leaves were considered too nu,merous, some of them would be cut out. Long rows of cultivated flax were seen at Aotea by early settlers. The withered outside leaves of a flax-plant are termed pakaivha. The half-dressed hukahuka or thrums of a pokeka (rough cape) are known as pureke. In former times the Maori had some curious ideas regarding flax. When making a flax- cultivation — i.e., setting out plants to form a pa harakeke — the planter was careful to note what particular wind was blowing at the time ; for when the flax was grown, and it was desired that use be made of it, then it was considered to be necessary to cut the leaves when the same wind was blowing as when the flax was planted, otherwise the fibre in the leaves would be found to be of a very unsatisfactory quality — short, weak, and brash. And if a person went to the owner of such a flax-grove and obtained permission to take some of it for his own use, his next question would be, " He pehea te hau i rumakina ai taua harakeke ? " (What was the wind when that flax was planted ?) And if such wind was not prevailing at the time, then he would wait until it did before cutting the flax. Now, if a person went to steal some cultivated flax, he would try the condition of the fibre in a few leaves. Should the fibre prove to be poor as to length and quality, he would know that he had gone a-thieving during the wrong wind. Hence he would wait until the wind changed, when he would try again. When he found that the flax gave a long, strong, desirable fibre, he then knew that he had hit upon the right wind — the wind that obtained when the flax was planted. Best. — Maori Forest Lore. 233 A somewhat similar superstition to the above seems to have obtained in regard to the mandrake-plant. In Lang's " Custom and Myth " we read, " ' In digging the root,' Pliny says, ' there are some ceremonies observed : first, they that go about this work look especially to this — that the wind be not in their face,' " &c. When the fibre of flax is prepared for weaving into a fine garment it must be carefully looked after. There are many dangers abroad in con- nection with the art of weaving : for instance, if that fibre be left at any spot where a person might step over it, it is a most reprehensible act of care- lessness, inasmuch as the fibre would never take the dye well if a person had stepped over it. When flax-fibre of the better grades is being prepared for the making of garments it is deemed extremely unlucky to throw the refuse of the leaves into a fire, for if that refuse be burned, then all the flax in the grove from which the leaves were taken will be spoiled. They will become kakara ivera — that is, the tops of the leaves will die first, then the whole leaf will become affected and die. I once heard an old Native woman exclaim peev- ishl}^, " Kiia kakara wera katoa taku pa harakeke i te mahi a te wahine ra " (My flax plantation has been ruined by this woman). On inquiry I found that the offending person had begged some of the flax, and had burned the refuse of the leaves after she had taken out the fibre. You will doubtless be relieved to hear that these restrictions, &c., pertain only to the higher- class varieties, those termed ivhitau or harakeke muka, and not to common varieties {harakeke maori). The term rnakuhane is applied to short, brash flax-fibre, the same being weak and easily broken : " Ka mahia te muka, na ka kotihe. Na te rnakuhane i loheraka ai.'" In former times long trumpets were made of flax by winding the green half-leaves in a spiral manner. They lasted merely so long as the material remained green. They were called tetere. Some old Natives state that flax was introduced into New Zealand by the Matatua migrants, w^hich is presumably an error. Leaves of the flax-plant, or strips of such leaves, were often used in certain rites of former times. When a person performed the rite known as matapuru, in order to preserve himself from the arts of witchcraft as directed against him by persons known or unknown, he first of all obtained some strips of green flax-leaf, which he tied round his body and limbs, perhaps three or four round each, in divers places. This tying-up process is termed ruruku. He then recited an incantation to avert the shafts of magic. This peculiar usage was often followed by persons visiting a distant village, when doubtful of the disposition or intentions of the people thereof. It would be carried out shortly before the travellers arrived at such village. When about to have the wai taua rite performed over them, the warriors of a war-party took off all their clothing, and each man tied a half-blade of flax round his waist. Under this belt in front each man thrust some green branchlets of karamuramu {Coprosma), which thus formed a sort of apron, which was known as a maro taua. The officiating shaman, or priest, then took a strip of green flax-leaf and walked into the water (stream or pond) wherein the rite was to be celebrated. He tied a knot in the middle of the iiax line and placed it in the water. If a stream, then the knot was placed up-stream. The priest stood between the two ends of the flax — i.e., in the bight of the line — while recitinsj his charms or spells. Ka kiia he kuwha tangata taua harakeke (That flax is likened to the thighs of a person). 234 Transactions. Again, when a Maori priest was called in to attend a sick person, one of his acts was to proceed to a clump of flax, where he pulled out one of the young leaves. If a screeching sound was made by the leaf as it was drawn out — a not uncommon occurrence — that was looked upon as a good omen : the patient would recover. This flax-leaf was placed upon the body of the patient when the priest repeated the charms by which he drove out the evil spirits, the cause of the man's illness. These malevolent demons were supposed to leave the sick person's body by way of the flax-leaf : hence, in tliis connection, it was termed an ara atua (demon-path). In modern times various preparations from flax have been used as medicines bv the Natives, for diarrhoea and other ills. In cases of difficult menstruation in women a peculiar decoction is administered : it is made by boiling four pieces of flax-root and four pieces of a plant known as al:a taramoa. For this complaint these materials must be taken from the east side of the plants, otherwise the medicine will possess no virtue whatever. In making a medicine for any other complaint the materials may be taken from any part of the plants. The roots of the huhi variety of flax are roasted and chewed as a cure for constipation. Scents. Under the above brief heading we propose to give a few notes anent the various scents used by the Maori in former times. These scents were various aromatic leaves and gums, used for the purpose of imparting a pleasing odour to persons or houses. Some were utilised wherewith to scent oil, which was then used to anoint the body. Fragrant leaves of various trees and plants were used for this purpose. The sense of smell possessed by the Maori is certainly keen, though they do not appear to object so strongly to foul odours as do we. The term kakara is usually employed to denote fragrance — any appreciated odour ; while the expression haunga would be applied to any smell not appreciated. The word kakara is also used as meaning " savoury," as when applied to food. The items used as scents in former times by Natives of the Tuhoe district were obtained from the following trees, shrubs, &c. : — Koareare ; sya., raukuwd. Panax Edgerleyi. Tunguru-rake. An Olearia. Kolara. Probably Olearia Cunninghamii. Tarata. PHtosporum eugenioides. Pna-kaito. Celmisia spectabilis. Kopuru. A moss. Karetu. HierocMoe redolens. There are other shrubs, plants, &c., that provided aromatic leaves for the dwellers in other districts, but the above are the items that obtain in Tuhoeland. Of these, the kotara and pua-kaito are found only at Maunga- pohatu, in the Tuhoe district, while the koareare and the tanguni-rake are found only on the high ranges. The leaves of the above trees, &c., as also those of the white manuka. were used in various ways. They were often enclosed in small bags or sachets, usually made of bird-skin with the feathers left on, which bag was suspended from the neck and hung down on the wearer's breast. The skin of the toroa (albatros) was prized for this purpose. The aromatic gum of the tarata tree was also placed in such sachets. Not only are the leaves of this tree most fragrant when crushed, but the gum that exudes from the Best. — Maori Forest Lore. 235 wounded trunk has also • similar properties. It is obtained by making an incision in the bark and wounding the trunk, thus causing it to bleed. The gum, on being exposed to the air, soon solidifies, and is removed. It was often used for the purpose of imparting a pleasant odour to oil used for toilet purposes. The oil used was obtained from the berries of the titohi tree {Alectryon excelsum) and from the fat of the wood-pigeon. Sometimes this oil was scented by placing in it crushed leaves of white manuka, or of the trees and plants enumerated above. A calabash of such oil scented with gum {pia tarata) was termed a taha tarata. The skin of a pukeko or other bird would be dipped in this oil and then rolled into a ball with the feathers outward. This was known as a pona tarata, and was suspended from the neck of the wearer. It was a somewhat greasy neck-pendant. Chaplets of the fragrant leaves, twigs, &c., were sometimes worn by women, and the sleeping-places or houses of persons of rank or of dis- tinguished guests were occasionally strewed with these aromatic leaves. The Jcotara and the pua-kaito were sometimes transplanted and grown near the Native hamlets. A gourd of scented oil used for anointing the hair was termed a taha koukou, from taha, a calabash, and koukou, to anoint. In an old Native song we find the following : — ■ • He wai tarata ra Me patu kia kakara Kia ingo mai ai. The last line explains one of the principal uses of scents the wide world over — viz., to attract the opposite sex. Women often wore belts made of the fragrant karetu grass. The flax belts which were made double were often filled with odorous herbs. Hence we see in song, — Tu ake hoki, E hine I te tu wharariki Hai whakakakara rao hiiie ki te moenga. We will now turn our attention to the fauna of the Tuhoe district — or, at least, that portion of it that entered into the domestic economy of the Natives of these parts. Lizards. The generic names for lizards are ngarara and moko. The following is a list of the various kinds found in Tuhoeland : — Tiiatara. Sphenodon puactatum. Koeau. Moko-ia. Moko-haJcariki. ? Xaultiniis elegani. Mokomoko. Moko-tapiri. ) j, ^Yf/ »///«».:* pacificus. These three names are applied to one and Moko-papa. - ^^^^ ,ame species. Ngarara-papn. } Moko-parae. The last-mentioned {moko-parae) is possibly a duplicate name for one of the preceding species. Again, ngaha was given as another name for the inokomoko by one Native, while another states that ngaha is a generic term, and includes the mokomoko, moko-parae, &c. The tuatara was the largest of these lizards, and it was the only species that was eaten by the Tuhoe Tribe. It is said to have been numerous on the mainland in pre-European days, and certain places were famed for the number of these lizards they produced. Such places were Wai-o-hau, 236 Transactions. Tawhiu-au, and Mount Edgecumbe. The latter hill is known as Pu-tauaki to the Maori. An old saying has it, " Ko Putauaki te maunga, he ngarara tona kai.'" There was no superstitious feeling among the Natives in regard to the tuatara and mokomoho, but it was deemed an evil omen to see any of the other species of lizards. At the present time the tuatara seems to have been exterminated on the mainland, and is in this district only found on the Rurima rocks, off Matata. It is there found, say the Natives, often living in holes in the ground or rocks wherein the kuia, a sea-bird, nests. Speaking of this bird, a Native said, " He iro nona a te tuatara " — meaning that the bird produces, or is the origin of, this singular lizard. At page 152 of vol. v of the " Transactions of the New Zealand Institute " is an account of the Moutoki Islet of the Rurima Group, wherein Captain Mair describes the haunt of the tuatara, and stat' s that two Ure-wera lads who accompanied him showed no signs of superstitious fear of ^ the tuatara. The lizard known as koeau to the Tuhoe Natives is probably the same as the kaweau of other tribes. Colenso states that it was known as tuatete in some districts. Local Natives describe it as being larger than the green lizard {moko-kakariki), as being light-coloured, and as living in the ground in winter-time ; also, that it stands high up on its legs, the under-part not sagging down on the ground as with other lizards. The body is also thicker than in other species. Mehaka tells me that the body of this koeau looks as though it were covered with a fine fur or down, and compared its appear- ance to that of a newly-born kitten. It is said to be about 9 in. in length. Another Native says that it is marked he mea ivhakairo, adding that, " When seen it is an evil omen ; disaster follows " {Kia kitea, he aitua, he kaupapa tahuri). It is also an evil omen to see the foeces of the koeau about your dwelling, or on your path when travelling, for that lizard represents the spirits of your dead relatives, who thus send you a sign to join them in the underworld. The koeau (sometimes called koea) is said to be extremely nimble, and could easily escape should any person endeavour to catch it — which is, however, the last thing a Native would think of attempting. If you take your eye off it for a moment it will have disappeared when yovi look again. It seems to have lived much on forest-trees. Tuhoean bushmen say that the iro, or embryo, of the koeau was sometimes found in rua kaka — holes in trees wherein the kaka parrot nested. It is a whitish or light colour at this stage. The koeau grows as large as a small tuatara. and grown specimens are of a reddish {puwhero) colour. The Native who gave the above notes added, " It is a very bad omen to see a koeau. Te Rangi-ua saw one, and, observe — all his elders have died." The moko-ta is said to be another name of the moko-kakariki. The moko-kakariki is the common green lizard. An old Maori myth has it that this lizard originates from the bird called kakariki ; that when the eggs of this bird are hatched out the portion of egg-matter left in the nest develops into an iro, or maggot, from which is developed the green lizard. The mokomoko is a small dark-hued lizard with a long tail. Buller gives the scientific name of this species as Tiliqua zealandica in the " Trans- actions of the New Zealand Institute," vol. ix, page 319. The moko-tapiri, also known as moko-papa and ngarara-papa, is said to be found in forest country, in holes in trees, &c. A carved representation Best. — Maori Forest Lore. 237 of this species on the large house Te Whai-a-te-motu, at Rua-tahuna, shows it of a short, squat form. It is said to be of a mottled colour. One very old man stated that it is about i in. or 5 in. in length, has a rough {wheketvheke) skin, and is light-coloured. Natives state that this lizard is the parent of the small cuckoo {pipiwharauroa). Another authority says that a kind of maggot found under the young chicks of the tihe bird in the nest develops into the moko-tapiri, which difi'ers much in appearance from the moko-kakariki, and is much feared by the Maori people. The moko-parae is said to be another name for the vioko-kakariki. The tara-kumukumu is said to be a species of lizard somewhat resembling a moko-parae, but it may be a marine creature. It has an unpleasant habit of afflicting mankind, and any complaint that causes a swelling in the region of the tliio'hs is attributed to it. This lizard is never seen now. It is some- times confused with the kumukiimu, a sea-fish, but the evidence is not clear. Lizards are said in Maori myth to be the offspring of one Punga, who was a descendant of Tangaroa ; hence the term te aitanga a Punga (offspring of Punga) is applied to reptiles. It is also applied to very dark-skinned or ugly, ill-favoured persons. The immediate offspring of Punga were Tu-te- wehiwehi, Tu-te-wanawana, and Kumukumu, the latter being a sea-fish. In Maori fable the latter adopts the ocean as its home, while the two former, representing lizards, keep to their land home. Hence the lizard said to the kumukumu (gurnard), " Go on your way to the ocean, but soon I shall see you caught and cooked for food." " Not so," remarked the latter, " but I shall see you destroyed by fire when the fern lands are burned." The lizard replied, " No one will injure me, for all will fear me on account of my appearance." Lizards are sometimes seen in the Native wood-carvings. One is so seen on a parata on a food-store known as Te Hau-o-puanui, at Rua-tahuna. In this case a lizard is hanging from the mouth of a carved human head, as though it were to replace the tongue. The tail of the lizard is in the mouth, while the fore part of the body, the fore feet, and head hang down below the chin. In the house Te Whai-a-te-motu, hard by, is the carved figure representing an ancestor named Kahu-tarata, which has a lizard hanging from the mouth in the same way. This ancestor is said to have been a noted eater of lizards. " Kg Putauaki te kainga, he ngarara tana kai " (Putauaki is the place where reptiles are eaten). This is an old saying applied to Mount Edge- cumbe and its environs, on account of the scarcity of food there. Tuatara were formerly collected for food, placed in baskets, and taken alive to the village, where they were cooked and eaten. " If women of the party ate of the tuatara they would suffer for it, and probably perish, for they would be assailed by many lizards of that species." So sayeth the Maori. " Ko te kekerewai, ko te tuatara nga kai o Wai-o-hau " [Kekerewai and tuatara were the foods of the Wai-o-hau district), said an old Native to the writer. The former is the small green beetle found on manuka bushes in summer. Lizards were sometimes selected as guardians of property or places in former times, presumably on account of the dread the Natives had of them. In some cases a lizard would be located on a tree much frequented by birds, in order to guard it against poachers ; or one was stationed near the forest mauri in order to protect or guard the same. In giving evidence in the Rau-ngaehe Block case Te Kaha said, " Te Purewa had a tutu (tree on which birds are snared) at Te Rua-ngarara, near Taumata-miere. A stage was 238 Transactions. made among the branches of that tree, and a lizard was kept at its base. Hence the place was called Te Rua-ngarara (the reptile's den)." Lizards were often selected or looked upon as the form of incarnation of a god or demon. Thus the god Peketahi, of whom Te Purewa was the human medium, appeared in the form of a lizard. Another such demon, known as Te Hukita, appeared in the form of a mohomoho ; while Tamarau, a deified ancestor who possessed the power of flying, is represented by a koeau. Insects and other " Small Deer." The generic terms for insects are manumanu and ngarara. In Native myth they are said to be the offspring of Punga, of whom we have already spoken — albeit some insects, &c., are credited with having other and ap- parently more immediate progenitors. Thus the mosquito and sandfly are said to be the grandchildren of Te Hekapona and Te Monehu, while the purerehua sprang from Fu-te-hue (origin of the hue, or gourd), the hihihihi from Hikawaru, the pmvereirere from Katipo, the ngaro from Moenga-nui, its offspring being Iroiro (maggots). Earthworms originated from Pane- wharu, whose younger relative was Mokoroa ; the next born was Whiti, and the next Tea. The enemy of these was Tangaroa (fish). The anuhe sprang from Nuhe. It was Nuhe who saw the fine markings of the tawatawa (mackerel), a descendant of Tangaroa, and forcibly took some of those markings for himself : hence the fine appearance of the anuhe. These marks are compared to certain patterns of tattooing. The anuhe and toronu are said to descend from the heavens — probably because their origin is not clear to the Maori — when they appear in great numbers on kumara plants. We give below an incomplete list of Native names of insects, earthworms. &c., as collected in this district : — Anuhe; syi\., hotete. A sj^ecies of caterpillar. Awheto. Cordiceps robertsii. HIJiue. Hawk-moth. Hiihu. ? Prionoplus reticularis. Kahukum. Butterfly. Kapowai. Dragon-fly. Katipo. A sjiider. Kekeremju. A bug or beetle. Kekereivai. Small green beetle seen on manuka. Kihikihi. Cicada. Kikihi. Cicada. Kowhiiiwhiti. Grasshopper. Kuharu. An earthworm. Kurekure. An earthworm {Tokea esculenia, Benham). Manumanu. Generic terra for insects. Moka. Caterpillar. Moko-roa. A grub found in houhi, mako, and kaiweta trees. Moko-tawliana. A caterpillar. Mu. Probably a species of spicier. Namu. Sandfly. Nyarara. Generic term for insects, lizards, &c. Xijaro. Genei-ic term for flies. Ngata. Slug, leech. Noke ; syn., take. Generic term for earthworms. Noke-tai. A species of earthworm. Ngoru. A species of earthworm. Ngutara. Cordiceps robertsii. Pakaurere. Winged grasshopper. Papaka. A species of beetle. Fepe The huhu at one stage of development. ? .Moth. Best. — Maori Forest Lore. 239 Pihareinga. Cricket. Said to be an introduced species. Pokorita. Ant. Pok-otea. An earthworm (Token uriwerce, Benham). Popokorik-i. [ ^j^^g_ Popokorua. ) Purerehiia. Generic term for moths, and possibly inchides butterflies not brightly marked. Puwereicere. | ^ ^^^^.^ Pumjawerewere. } ' Ro ; syn., ivhe. The mantis. Tai. (See Noke-tai.) Tarao. An earthworm {Rliododriliti< ediilis, Benham). Tarapoa. A large moth. Tataka. (See description of /;»/;».) Tititi-pounamu. Katydid. Toke. Generic term for earthworms. Toke-rangi. Bhododrilus besli, Benham. Toronu. A species of caterpillar. Tuiau. A species of midge. Tunga. A grub. Tunga-rakau. I g^^ ^^^^^^^^^ ^^ j^^^j^^^_^ 1 unga-rere. i ^ Tungoungou. The larva or chrysalis of the /ti^?/e. Tutaeruru. Some winged insect. Waeroa. ilosquito. Wham. A species of earthworm. Weri. Centipede. Weta. An insect. Whe ; syn., ro. Mantis. Whiti. -A. species of earthworm. A foolish or foolliardy person is compared to a moth that flies into a fire. If many moths are seen around a fire at night, such is deemed a good night for eel-fishing. The awheto is known to us as the vegetable caterpillar {Cordiceps rohertsii ; also, apparently, known as C. hugelii). In its living state it is known as ngutara. When it burrows into the earth and there dies it is termed awheto. These creatures are collected and burned and used to make a black tattooing- pigment. The hihue is classed as a purerehua by Natives : it is the hawk- moth. The larva or chrysalis of this species is found underground, in which state it is called tungoungou. When it acquires wings it is found upon the white blossoms of the hue or gourd-plant (but not on those of pumpkins). Natives state that it thrusts its proboscis down into the flowers in order to draw up the liquid found therein, and that it received its name from this act {hi, to draw up). The huhu is a grub found in such timbers as rimu, tnatai, and kahikatea, which it attacks at the first sign of approaching decay, as when one of these trees has been scorched by fire. In its grub state this creature is known as tunga-rakau ; when it ceases to bore, remains in a cell, and casts its skin, it is termed tataka. When its legs and wings are formed, though still white, it is known as pepe. W^hen it emerges from the tree or log and flies about, a brown cockchafer, it is called tunga-rere. In its grub state this species is prized as an article of food. Butterflies are called kahukura, though possibly the name is applied only to bright-coloured species. The katipo is a species of puwerewere, and is found on the coast, but apparently not inland. It is often found about tauhinu scrub. Its bite is much dreaded, and seems to cause considerable pain. The Native cure for katipo-hiie^ is to hold the afflicted person over 240 Transactions. a fire which is made to give forth much smoke, the process being known as ivhakapua. They were also often laid in a stream, so that the body was covered with water. The l-ikihi, or Jcihikihi, or hihihitara, is the cicada or singing-locust. Said an aged Maori to the writer, " I will give you the song of a certain people of this world : those people are the kihikihi. They are an exceed- ingly numerous people. During the ivaru pcdote (eighth month of Maori year) those people cling to their ancestor, Tane-mahuta (settle on trees), and sing lustily. Here is the song of those people : — "Kaore te waru nei Ka pii i ail ki ^a Tane-mahuta Ki tokii tupuna Til takere ! Tu takere ! lere nui au Kohiti ko Makaro, iere au Popo nunui. ]iopo roroa. ko wai e aha atu Xa Tane ano au i awhi ki tua te aiorangi l\a whiti mai ko te iwa Ka hoki au ki raro ra ki tona kainga Maua tahi ko taku taina ko Xuhe I tonoa iho nei ki tona tungane, ki a Rongo Hei manawa niona Koia ka tumoumoutia — ha ! " The cicada is treated in Maori fable as the personification of slothful carelessness, and the ant as the emblem of industry and forethought. Fable of the Ant and the Cicada. The pokorua (ant) said to the kihikihi (cicada), " Let us be diligent and collect food during the summer, that v^^e may retain life when the winter arrives." " Not so," remarked the cicada ; '' rather let us ascend the trees and bask in the sun on the warm bark." Even so, the ant laboured at collecting and storing food for the winter. The cicada said, " This is true pleasure, to bask in the warm sitn and enjoy life. How foolish is the ant, who toils below ! " But when winter came, and the warmth went out of the sun, behold, the cicada perished of cold and hunger, while the ant, how snug is he in his warm home underground, with abundance of food ! As the cicada clung to his tree, rejoicing in the warmth of summer, he sang, — He pai aha koia taku pai He noho noa Piri ake ki te peka o te rakau E inaina noa ake Ki te ra e whiti nei Me te whakatangi kau i aku paihau. The following is said to be the song sung by the industrious ant : — Hohoro raai e te hoa Kanaka e whakaroa ara ra Ka turua ta te poi)okorua Rawe noa tangata ki whakahaiihau — c Ki te keri i te rua mo te ua o te rangi Mo te makariri wero iho i te po nei — e Me te kohi mai ano i te kakano — e Hai ora mo taniaroto, kia ora ai — e. The term purerehua (also purehua) is applied to moths generally, and perhaps also to butterflies of quiet colouring. Some species of purerehua were formerlv eaten by Natives. The mokoroa is a grub found in hoiihi, mako, and kaiiveta trees. The mu is said to be a form of spider. Best. — Maori Forest Lore. 211 The namu, or sandfly, is a relative, of the mosquito, according to Maori fable. They are descendants of Haumia and Te Hekapona, and children of Te Monehu (monehu, syn. mokehu, young shoots of the common fern, rarauhe). Other such descendants are the ro and puwerewere and other such insects. Namu-iria, a son of the namu, stole the hau, or vital essence, of Tu (god of war and origin of man), for which he was slain by Tu. Hence the sandfly people declared war against Tu — that is, against man. They still assail man in this world. They are exceedingly strenuous in their attacks upon man. The moscjuito fears but two things — wind and smoke. The mosquito said to the sandfly, " Let us wait until evening before we attack man, lest we be slain. Then we will attack him, and I will buzz in his ears." But the sandfly would not consent to this. He said, " Though myriads of us be slain, yet will we give battle in the light of day. Though we perish, what matters it so long as we shed the blood of man ? " Even so they went forth, and were slain in their thousands. The mosquito ob- served this, and said, " I told you to wait until nightfall. Now see how you have suffered." E ki ana ahau, e taku tainaina VVaiho kia ahiahi ka haere ai taua Ki te riri i to tuakana Ki rawa atu au : Waiho kia mam ahiahi Hei wheowheo i ona taringa. Such was the song of the mosquito to the sandfly, and to which the latter replied, — He ahakoa, e taku tuakana Te mate ai au I ana toto ka pakaru kei waho — e. (And you, 0 mosquito, when you assail man at night, will be smoked to death.) Xoke and take are generic terms for earthworms, of which a good many kinds have special names. The papaka appears to be a kind of beetle. The toronu is a kind of caterpillar which formerly infested the kumara plants, and gave considerable trouble to the neolithic agriculturalist. A day was set apart by the sorcerer priests for the destruction of this pest. It was brought about by means of a rite known as ahi patu toronu. You might like to know how it was that the crops of man came to be assailed by these pests. When the kumara was first obtained by mankind it was stolen by one Kongo-maui from Whanui (the star Vega), who seems to have been the custodian of that prized tuber. In a spirit of revenge, Whanui sent Nuhe (anuhe), Moka, and Toronu down to earth to destroy the kumara cultivated by man. These are the three species of caterpillar that prey on the kumara plants. The tutaeruru is some form of winged insect, perhaps a beetle, which flies around in the evening with a booming sound. This species and the kekerewai were sometimes called the manu a Rehua. They were both eaten in former times. In some districts tapapa is a lizard-name, but which species it applies to I cannot say. MOLLUSCAN Fauna. I have collected a good many forms of land-shells in the Tuhoe district, the specimens being examined and named by Messrs. H. Suter and C. Cooper. They are of small size, with the exception of one, known as pipiko to the 242 Transactions. local Natives, which is found up to about | in. in diameter. I will not annoy the guileless reader with a list of the above names. The fresh-water shell-fish of this district are not numerous. The kalcahi, or fresh-water mussel, is plentiful in Wai-kare Moana, and is also found in i^onds at Te Papuni, Ruatoki, &c., but is not numerous elsewhere. These formed an article of food formerly, but are very insipid. Unio zelebori, from a pond at Te Papuni, has a very thick, heavy shell, that district con- taining limestone, which is not seen west of Maunga-pohatu. Unio menziesi (Gray), from a lagoon at Ruatoki, has a thin, fragile shell. Specimens obtained at Wai-kare Moana do not seem to be the same as Unio waikarense, described by Colenso. The latter are light-yellow, and larger than those collected at the lake by Mr. Lucas and myself. The koura, or small fresh-water crayfish, is not found in the Tuhoe district, so far as I am aware, save at Te Houhi. The fish found in the rivers and streams of the district are eels, kokopu. marearea (syn. inanga), titarakura, papanoko, and the upokororo. The last-mentioned has now disappeared. Duplicate names of some of these species, as also names of varieties (from a Native point of view), will be found in a previous article on " Food Products of Tuhoeland " in this journal. The Kiore, or Native Rat. The kiore maori, or native rat, is said in Maori tradition to have been imported into these isles from Polynesia by the early migrants who settled on these shores, and was not an indigenous animal. These small creatures furnished a considerable amount of food to the forest-dwelling Native tribes in former times, their flesh being highly esteemed. The kiore maori is said to have been a clean and even fastidious eater — unlike the introduced rats — and henc6 its flesh may well have been very good eating. Many persons stoutly maintain that the old Maori rat is still with us. has not yet died out ; but it seems probable that they mistake the black introduced rat for the old-time kiore. A writer in the Canterbury Times newspaper states that enormous numbers of Maori rats appeared in the northern part of the South Island in December, 1884. These creatures cannot have been the kiore maori, but must have been the black rat alluded to above, or some other introduced species. I have never heard that the native rat ever appeared in such migrant swarms. The above writer refers to his native rat as Mus exulans, and says, " The kiore is smaller than either of the two rats introduced into the colony by Europeans, and the female is somewhat smaller than the male. Their average weight is about 2 oz. The fur on the upper portions of the head and body is brown finely mottled with dark-grey. The sides of the body are lighter, and all the under parts, including the chin and the feet, are dirty-white. The species is found throughout Polynesia. In New Zealand it is sometimes called the ' bush-rat.' The proper name is Mus exulans.'' This article seems to have been taken from a paper by John Meeson, B.A., published in vol. xvii of the " Transactions of the New Zealand Institute." He states that the following species of rat are now (1884) found in New Zealand : (1) Mus decumanus (Norwegian rat), which has driven away the kiore maori into remote districts, if it has not exterminated it altogether : (2) a species of Mus rattus ; (3) a smaller species (Professor Mutton's Mus maorium). The writer believes that the migrant swarm of 1884 consisted of the third species {Mus maorium), and that this was the old-time kior( Best. — Maori Forest Lore. 243 maori, though this statement scarcely agrees with his remarks (see supra) on Mus decumanus. Mr. Meeson thinks that there may have been two species of native rats. Dr. Buller's Mus novce-zealandice (Trans. N.Z. Inst, vol. iii, page 2, 1870) had ■' fur above bluish-black." This he claims was a specimen of the old More maori, or native rat. But this description seems to fit a bluish- black bush-dwelling rat now found in the Tuhoe or Ure-wera district, and which the old Natives say is not the old native rat, but one introduced by Europeans. My local information on this subject was obtained from two old men of the Tuhoe Tribe — Tutakangahau, born about 1830 or 1832, and Te Puia Nuku, who seems to be some years older. They both belong to cannibal days, both saw the old hiore maori in their youth, saw it die out, and the two introduced species overrun the land. Dieffenbach, writing in 1843, said, " The indigenous rat has now become so scarce . . . that I could never obtain one." Tamarau Waiari, an old man of the Tuhoe Tribe, who was born in 1830, said that the old native rat disappeared in 1838 from the Ure-wera district. Though all the old men state that it rapidly disappeared after the im- ported species reached this district, yet it is improbable that it was exter- minated in the space of one year. It may have been last trapped or last seen in 1838, or the imported rats may have first invaded this district and com- menced to wage war against the kiore maori about that time. Anyhow, all agree that shortly after the arrival of the imported rats in this district the trapping of the native rat was given up, so scarce had they become. Judge J. A. Wilson states that the hiore was unknown to the original Polynesian people of New Zealand ; that it was not imported until the arrival of the last migration. This seems highly probable. It appears, however, that rat-bones have been found mixed with moa bones in the South Island, and also in a subfossil state. The two species of rat found about my own primitive camp in the Tuhoe district, and which are bold and troublesome in winter-time, are the grey Norwegian rat (so called) and a bluish-black rat which I take to be Mus rattus. The former appears to be an omnivorous creature, and eats leather, with relish apparently, at times, and has of late made a hearty meal off an Angora-hair saddle-cinch. Mr. Taylor White speaks of the kiore maori as being of a grey colour, and smaller than the so-called Norwegian rat (Trans. N.Z. Inst., vol. xxvii, 1894). In vol. xxviii of these Transactions, page 3, Professor T. Kirk says, " The place formerly occupied by the Maori rat in the North Island is now so fully occupied by its old enemy the black rat as to afford a striking instance of complete replacement." The above writer states that the Mus maorium of Hutton is the old-time native rat, or kiore maori, and that it still survives at various places, north and south. The origin of the rat, according to Maori myth, is as follows : " The origin of the kiore maori was one Hine-mata-iti, daughter of Pani (the parent or producer of the kumara, or sweet potato)." So said old Pio of Ngati- Awa, of Te Teko, born about 1824. Again, he says, " The first fire given by Mahuika to Maui was the little finger (to-iti) of her left hand. That to-iti represenJts Hine-mata-iti, who was the matua (parent) of the kiore.'''' And again, " The ancestor of the kiore was Pani-tinaku — that is to say, a female child of Pani's. Her descendants are the kiore, who are a very numerous people. The reason of their being assailed (by man) was because 244 Transactions. they began to steal the grandchildren (offspring) of Pani-tinaku — that is, the kumara.'" And again, Pio says, " Tenei iwi te kiore, ko Hine-tnata-iti.'" The Rev. R. Taylor, in " Te Ika a Maui," gives Hinamoki as the creative parent, or origin, of the rat. We shall mention this term again. We give below a list of Maori names for rats : — Hinamoki. Matapo. ir .■ . - These names are known to the Tuhoe Tribe. M unfa I. I Poti-o-hawaiki. Toknroa. Hamua. Given by John White. D ■ ■ '^ ' ■ ■ Given in Williams's Dictionary. Mir 01. ) •' Kiore. Generic term. The hinamoki is said by Paitini, of Tuhoe (who was born about the year 1843), to be the name of the old-time Maori black rat. He used the term pango to describe its colour, but this term is used to -denote dark-brown, dark-blue, &c., as well as black. He stated that the hinamoki is extinct, but that a pango (black, or dark-coloured) foreign rat took its place. He himself has never seen the old Maori rat ; it was extinct before his time — i.e., before he can remember, not necessarily before his birth. Some years after giving me the above notes he told me that the hinamoki was a dark- coloured rat, a bluey-black. Williams's Dictionary simply says, " Hinamoki, a kind of rat." This is terse, and, if not sufficient for our purpose, at least shows the cautious mind of the lexicographer. But Mr. Taylor White (Trans. N.Z. Inst., vol. xxvii, page 259) is not bound by earthly rules, and says, " Investigating the structure or composition of hinamoki, we find hina, grey hair of the head — which would seem to mean white rather than our standard of a grey colour, as of a rat or rabbit. If .so, it seems hardly applicable in this case. But hina is a personification of the moon, and supposing the original form to have been mokai, rather than moki, we have ' Hina's pet' — the animal moving about at night." This is lovely ! But why not carry the matter out to the bitter end — I mean, its logical conclusion ? Observe : If the original form of hina was Paraone, and moki but a modern rendering of kau, then, on the lines of the above reasoning we have "Brown's cows" — which, after all, may be but an overgrown species of rat. There are endless possibilities in the hinamoki. And, besides, I know to my bitter cost that cows do move about at night. 'Twas but Monday se'nnight that, as Parearau sagged down on Tokorangi Hill, .they (those cows), with evil in their hearts, did make entry into my truck-patch and work much havoc therein, strolling forth therefrom, as the blushing sun rose, followed by divers potsherds, brickbats, and choice profanity in three tongues. Kali! Enough! A truce to these idle jests. Here endeth the hinamoki. * Matapo. — Old Tamarau Waiari, of Tuhoe, told me that there were two kinds of native rat in former times — the matapo, a black or dark-coloured {pango) species, and the tokoroa, a grey rat. Whether these were two dis- tinct species, or the greyness of the one simply the result of age, it is now impossible to ascertain. Tamati Ranapiri, of Ngatiraukawa, told me that the matapo was an old-time native rat, but he did not know the name tokoroa as that of a rat. Moke. — Paitini, of Tuhoe, said that the moke was a native rat, but some years after said that it was the name of the light-coloured European rat (Norway rat), so that his evidence is doubtful. Bkst. — Maori Forest Lore. 245 Muritai. — This was given me by a Tuhoe Native as a name for rats, but he said that it was not used in this district, and that he did not know whether it applied to the native rat or an introduced species. Akuhata te Kaha, of Tuhoe, says (27tli August, iy()8), " The muritai is the same as the moke. This species always travelled along their runs in single file, and closely following each other. The fur was dark-coloured (piipanqo), but not black. He ahua fufamp nga huruhuru o te muritai. The hinamoki was pango (black, or dark-coloured)." Pou-o-hawaiki, sometimes pou-hawaiki. — Old Tutakangahau, of Maunga- pohatu, a good authority, said, " I saw the native rat die out in my youth. We called the introduced European rat the pou-o-hawaiki. When I was a lad I went with a party to the summit of the main range at Maunga- pohatu, in order to obtain mutton-birds. On our arrival there we found that a new species of rat had appeared, and had eaten all the young birds." This witness was born about 18.30. Paitini says that the introduced black rat was named the pou-o-hawaiki by the Maoris. Mr. White quotes several authorities in his aforementioned paper as to the application of this Native name. Some applied it to the black rat (presumably Mus rattus) and some to the old-time native rat, but the best authority (old Tautai, of Taranaki) said it was the introduced Euro- pean rat. Unfortunately it is not made quite clear as to whether Tautai meant Mus rattus or M. decumanus. Williams does not give this Native name, but Mr. White has its derivation all fixed up, albeit it was necessary therefor to alter the spelling of the word from its proper form : " po= night, hawaiki= the far country; and the combination means that the beast was a mysterious visitor from an unknown land shrouded in darkness." Having of late been sadly shaken by hinamoki and the identification of the ancient Pani-tinaku with Espani (? Spanish), I cannot quite grasp this matter. Was it the beast or the land that was shrouded in darkness, or were they both so shrouded ? Tokoroa. — Already referred to (see supra). Hamua I know not, except the mention of it in John White's works as a name for rats. Maungarua and riroi I have not heard of among Tuhoe. We will now give a few notes touching upon the old native rat, as ob- tained from members of the Tuhoe Tribe. The kiore maori, or native rat, nested in hollow trees, and also in bur- rows in the ground. They came out only at night, remaining in their holes in the daytime. They were more plentiful in hunua forests than in those termed uruora — that is, they preferred the high-lying forests to those of the valleys or other low lands. Their favourite resorts were the beech forests which occupy the summits and upper parts of the ranges of Tuhoeland — roughly speaking, from about 2,000 ft. altitude upwards. Their principal food consisted of hua tawai, or beech-mast. Great quantities of these nuts are produced by the beech forests of the high lands. The rats came out of their holes at night, and marched in single file along the ara kiore, or rat-runs, to their feeding-grounds. Besides the beech- nuts, they also ate the berries of the patate {Schefflera digitata), the para (1 pollen) of the kahikatea or white-pine, and some other items. They appear to have been clean-eating creatures, avoiding foul matter, and re- sembling a squirrel so far as their food was concerned. They became very fat in winter-time, and were then trapped and snared in great numbers by the Natives. They became quite thin in summer-time, and were not taken in that season of the year. 246 Transactions. The nra kiore, or rat-tracks, made by these small creatures to their feeding-gromids always ran along the summits of spurs, ridges, or ranges, and were often many miles in length, though it is unknown as to how far a colony of rats would ramble from their abode in search of food. They used the same tracks year after year. These tracks are sometimes termed ara tahiti ( = taivhiti), or trapping tracks or runs, because the traps for taking the kiore were set on them. These tracks or runs were about 3 in. in width, and were smooth, and padded by myriads of little feet : thus they were quite bare, and void of vegetation. The traps — of which more anon — were set every 3 ft. or i ft. along the run. A rat-run might be owned by many different persons, and long ones by different hajm or sub- tribes, each person interested having a right to a well-defined portion of the same. Poaching on another's portion was not permitted, and would cause trouble, possibly fighting. As a general rule, among the Tuhoe Tribe these rat-trail privileges were acquired or retained by the female members of a family or gens, the males getting the toroniiro trees (on which birds were snared). When the rats, in passing along their runs, bit off leaves of vege- tation and dropped them on the track, then it was known that they were in good condition, fat and plump ; hence the trappers would get to work, and the rat season was opened in due form. An experienced trapper, on observing the above-described signs, would say, " Kua whariki te ara kiore " (The rat-run is covered). " Na, kua momona te kiore " (Then it was known that the rats were fat). An ancient saying is, " Kua kitea a Matariki, a kua maoka te hinu " (When Matariki is seen, then game is in good condition). This, I believe, applies to the heliacal rising of Matariki (the Pleiades), which would mean that the game-trapping season opened early in June. It would appear that the Maori noted the heliacal rising of stars as signs of divers events, &c. " The appearance of the Pleiades on the eastern horizon just before sunrise, in June, marked the commencement of the Maori year," says Tutakangahau. The appearance of Whanui on the eastern horizon in the morning was the signal for lifting the kutnara crop. Whanui is the star Vega. Kiore were trapped on the dark nights of the moon. If the traps were set on moonlight nights, then the rats sprung the snares and escaped {ka turupanatia mja tahiti e te kiore). In Taylor's " Te Ika a Maui " may be found some notes concerning the kiore maori. He gives two of the karakia, or charms, used, one of which is a taitai, but the translations thereof are doubtful. He also states that the hunting-parties cut tracks for the rats, which tracks were made in a per- fectly straight line up hill and down, however rough the country, other- wise the rats would not follow them. I cannot get any old Maoris to agree to this statement, and hence do not believe it. The kiore made its own runs, which were assuredly not straight, for they followed the tops of ridges, with all their dips, angles, and sinuosities, trappers made no tracks for the rats. The kiore maori was taken in two ways in Tuhoeland — by tahiti (trap or snare) and by the torea (or pit). Of these, the tahiti appears to have been the most frequently used. The most general form of this word is tawhiti, l)ut Tuhoe always use the form above given, even as they use hitau for whitau. Williams gives " Tawhiti = a snare, trap." Another form of rat- trap was termed a pokipoki. These two forms we will endeavour to describe. Best. — Maori Forest Lore. 247 Tahiti hiore. — The two rupe are first placed in position. These are two pliant wands. One is forced into the ground at both ends, so as to form a small archway across the rat-track. ' The other is erected close to it, in a similar way, but is twisted round the first one so as to leave a narrow space between them at the top, through which space the two main turutvru, or uprights, are passed, as also the loop snare. These rwpe are usually pieces of 'pirita (supplejack, a climbing-plant). Twining one round the other prevents them' from parting or becoming too loose. The two main uprights (tunituru) are thrust down through the uppermost space between the two rupe, one on either side of the central opening or passage, which passage is on the rat-run. The other uprights are simply stuck in the ground out- side but close against the rupe, and are placed close enough together to prevent a rat from passing between them. The only space through which a rat can pass is the central one on the track, in which space the snare loop is suspended. The whana, a strong pliant rod, usually a piece of supple- jack, has one end thrust securely into the ground, and to the other end is attached the tohc or looped ^cord. This small cord is not formed into a 1. Aho. 2. Tohe. 3. Ku rnpae. Tahiti Kiore. 4. Taralara. 5. Tunituru. 6. Rupe. 7. Whaim. running noose like that of a bird-snare, but has both ends attached to the ivharia or spring stick, so that the rat is caught in the bight of the cord. Also, attached to the end of the whana by means of a string is the taratara, a piece of small stick about i in. in length, and with which the trap is set. The string {aho) or cord is fastened to the taratara about ^ in. or | in. from the end of the latter. In order to set the trap, the operator bends down the tvhana and passes the tohe or looped (doubled) cord down between the two rujje until that cord nearly touches the ground, the loop being arranged so that the cord hangs close to the two main uprights on either side and does not obstruct the passage. The trapper then, while holding down the spring stick with one hand, takes the taratara in the other, and places it in a vertical position at one side of the open space, near the upright. The projecting upper part of the taratara is placed on the opposite side of the rupe to that on which the securing-cord {aho) is, so that the rupe •rests in the crotch at X. The trapper then holds the taratara in a vertical position while he slips the kurupae, a small, short stick, between the lower end thereof and the two main uprights. The J 248 Transactions. strain on the taratnra holds the kurupae in position until the latter is forced down, and free, by a rat endeavouring to pass over it through the space, and so along his old-time trail. The kurupae is near the ground, so that a rat cannot pass under it. When he treads on it, the pressure forces it down, releasing the taratara, the lower end of which flies upwards, and the upper end slips away from the rupe. Thus the ivhana is released and springs upwards, drawing the looped tohe up between the two rupe. But Master Kiore is right there in that loop when it is released ; hence his body is yanked upwards and jammed against the rupe, there still being a certain amount of strain on the loop-cord (tohe) and ivkana. The latter cannot become wholly free while there is any body in the tohe large enough to stop its upward passage through the two rupe. The strain of the whana is primarily on the aha, then on the taratara. There is the upward pressure of the latter on the rupe and the side pressure on the kurupae. Q.E.D. The aha passes down outside the rupe. The tohe hangs loosely ; there is no strain upon it until a rat is caught and jammed against the rupe. Kati. Kua marama pea ! No bait is used when setting these traps on the runs or tracks, but a bait is used when they are set away from them, as on the feeding-grounds. The bait used was the fruit of the patate tree. It was placed on the ground near the trap, and on the opposite side to that from which the rats were thought to be likely to come. When a rat was caught by the loins it was able to move to a certain extent, and would endeavour to free itself by gnawing the rupe or the snare loop. These hiore kai apuapu, as they were termed, should they escape, would never be caught again, say my informants : they became too knowing. The ivaharua was a rat-trap having two entrances — a double trap, which faced two ways. It w^as really two traps like the one above described, erected a little distance apart. The side spaces between them were blocked with little fences of upright sticks. The tahiti ivhakaruatapu (cf. ruatapu in Tregear's Dictionary) was a rat-trap having several entrances thereto, and a snare for each. This I have not seen, but the others have been constructed for my benefit by several old Natives. When rat-trappers were setting their traps on an ara tahiti they would carefully remove any leaves, &c., that had fallen on the rat-run. We now come to that form of rat-trap known as a pokipoki. This form of trap was used to take those suspicious or cunning rats that declined to enter the ordinary trap. They seemed to object to passing over the kurupae. Like Brer Rabbit, they were " some cautious " and " plenty scared." In fixing this trap the rupe are fixed as before, but the turuturu — gene- rally only two of them — are longer. They are inserted in the same manner, and the upper parts, that project above the rupe, are bent back, half broken, until their ends rest on the ground. The large leaves of the ivharangi tree are then used as a lining for the little trap-house behind the rupe. These leaves are placed over the bent-down ends of the uprights by which they are supported. Other leaves are used wherewith to block up the front of the trap, with the exception of the central space, where hangs the snare loop, and through which the rat attempts to pass when it sees the bait within. The diminutive enclosure is then covered over with some loose earth, until it resembles a little mound, sloping downwards to the back end. This little hut, or rua as it is termed {rua = tunnel, cave, hole, pit), is about 8 in. long, and the bait is placed a few inches back from the entrance, inside. Best. — Maori Forest Lore. 249 The katara, or small uprieht stick, is thrust down through the roof until the lower end is just above the floor of the little hut. To this lower end is secured the bait of patnte berries. One end of the ichana, or spring rod. is thrust into the earth ; to the upper end is secured a double cord or loop, knotted near the middle. This is the tohe, or snaring-loop. The cord termed ivhiti is secured at each end to the rwpe, on either side of the entrance. To set the trap, the upper end of the whana is bent down, the lower loop being passed between the two rupe, and arranged as in the common trap. The kunipae. a short stick, is slipped under the whiti cord and through the 1. TP7(o?io, spring stick 5. Katara. 6. Whiti cord. Rat-trap, Pokipoki. 2. Upper loop of to/«e cord. 3. yoAe, or snare loop. 4. Kurupae. . Rupe. 8. T'uriituru. or uprights. 9. Knot of loop. upper loop of the tohe, the rear end resting on top of the katara. The whiti cord is between the tohe and the katara. Thus the whiti saves the situation, takes the upward strain of the whana until a rat, pulling at the bait, tugs the katara outwards, thus releasing the kurupae, which flies off into space. The bent ivhana flies up, dragging up the looped cord, and jamming the rat against the rupe, as before. While the trap is set the strain on the tohe is, of course, on the knot, the lower end hanging slack. When the trap is sprung the strain is on the rat. The next act is the arrival of John Tenakoe, who pops Mr. Kiore into his game-bag and resets the trap. The torea, or kopiha kiore, is the pit trap for taking rats. The first of these two names is the one in common use among the Tuhoe Tribe. The following was the modus operandi in this district. A hole or pit about 4 ft. deep was dug in a suitable place. Some bait was placed at the bottom of the pit, and a piece of wood was placed in the hole in a slanting position, and down which the rats travelled in order to get at the bait. After the food so placed foi them was consumed the rats would return above ground by the same route and go about their other business. After the rats had got accustomed to going into the pit for the food the ladder was taken away, and a number of slight sticks were stuck in a hori- zontal position into the ground at the mouth of the pit, so that each stick projected out over the mouth of the pit. On the end of each stick a bait was tied. The rats walked out on these sticks in order to Entrance to a Torea Pit Trap BAITED. 250 Transactions. get at the bait, but so slight were the sticks that it was impossible for the rats to turn or return upon them, hence they fell into the pit beneath. Sometimes a cooked bait was used instead of berries. Presumably the bait of cooked food was the more savoury, and attracted more rats than one of ripe berries. Pio, of Ngati-Awa, born circa 1823, says, " This is about rat-killing. Hine-mata-iti was the origin of the rat folk. A pit was made, food was roasted (as" bait) in the evening, and stuck on sticks in the middle of the pit. At night the rats go to eat it. The trappers go and iind a pit full of rats. They are slain and placed in baskets. Two, three, or four basketfuls may be secured in a night. I trapped rats in the days of my youth. It was interesting work. The rats were very fat." An interesting note was given to me by Tamati Ranapiri, of Ngati- Raukawa, anent the genial kiore maori : " There were two ways of taking rats — viz., by the tawhiti, and by digging a pit. A pit would be dug some 4 ft. or 5 ft. in depth, and in such a manner that the top overhung, the pit being wider at the bottom than at the top. A peg was inserted at the bottom of the pit, to which w^as attached the cords by which the rats descended. Food was placed in the pit as baits, such as berries, &c. When this bait was consumed, then more would be thrown in. That same night the trap would be visited, and the rats slain. The trapper would know right well the par- ticular cord by pulling which he could haul up all the cords, or aka, placed for the rats to descend by. By pulling this cord he hauled up all the cords, as also the peg to which they were fastened at the bottom of the pit. He then jumped down into the pit and killed the rats. After these rats were taken out the pit was swept and cleansed, so as to do away with the smell of rats, and so that other rats would enter the pit when it was rebaited. I have heard that the kiore swam from Hawaiki to Aotearoa (New Zealand), that they swam hither together. A leader swam in front, the next rat took the leader's tail in his teeth, the next took the tail of No. 2 in his teeth, and so on to the last rat." In the above we note that, among Ngati-Raukawa, cords or forest creepers were used as rat-ladders in the pits. The final remark, about rats swimming hither from Haw^aiki, is of interest. In an article already quoted (Trans. N.Z. Inst., vol. xvii, page 200), Mr. Meeson mentions a swarm of rats that swam across the passage leading into the harbour at Nelson. The lemming of North Europe is said to have swum out to sea in hordes. Hurae Puke- tapu and other Natives of Wai-kare Moana have informed me that in former times, when the native rat was numerous in those parts, they sometimes took to the water in numbers. On misty nights, when fog lay close on the waters, the rats, frightened by the cries of the ruru owl, would swim out into the lake until they were drowned. Some say that the native rats would so take to water when the pollen(?) of the tawai tree lay thick on the water's surface. Return w^e to our tahiti kiore, or rat-traps. Te Puia Nuku, an old man of Tuhoe, who was a fighting-man in 1852, and died on the 20th December, 1906, told me that on the opening day of the rat-trapping season all the trappers were tapu. As a man set his first trap he would repeat over it the following charm : — Kiore — e — e ! Hai konei ra piko ake ai I te whare nui, i te whaie roa E tataia e te mahanga Ko rua hamuti te kiore Te mau ana. Best. — Maori Forest Lore. 251 This was repeated over the first trap set only. In Nga Moteatea another version of the above gives the first line as " Tawhiti — e ! " which reads better. Te Puia p\it it, " Ka oti te rafiko, la harahia i tenei,'" &c. (When the trap was set he recited this). The words whapiko, tapiko, kopiko, and rapiko, which seem all allied to and bear a similar meaning to whakapiko ( = to bend), are all employed to denote the forming of looped snares and the bending-down of the ivhana in trap-setting. The trappers, on returning to the camp or hamlet on this first day of the season, w^ere obliged to be very careful in their behaviour. They might not speak for the balance of the day and following night. They ate their food in silence, and slept without removing their garments. The next morning they went to take the rats from the traps. The tapu was then lifted from them and their employment, and they returned to their normal condition. Tutakangahau stated that the tapu of opening the rat-trapping season was similar to that pertaining to birds. When a good many rats had been taken on the first day, and collected, a time was appointed for the huhuna or icJiakanoa rite (lifting of the tapu, the making common, opening of the season). This function often continued for two days. There were many karakia (charms, invocations, &c.), says Tu, pertaining to the opening of the rat. fish, and bird taking seasons, taking the tapu off the forest, &c. Some of them came under the generic term of kaha. Such were the tumu- tumu, the tuota, and the motumotu. The tuota was a very tapu charm, re- cited in order to bring plenty of rats, birds, or fish to trap, snare, or net. If a hunter employed this kaha he would deem it necessary, on his return from the forest, to perform the vJuoKjai rite. This was an offering to and placation of the atua (gods, demons). The motumotu was a noa charm, free from tapu, and could be used by any person, but its object was the same as that of the tu-ota. It might be asked of a fowler, fisher, or rat-trapper, " Ko wai to kaha ? " (What is your kaha ?) and the answer would be, " Ko tuota " (It is tuota), or " Ko motumotu " (It is motumotu), or which- ever it was. The following charm or invocation used in trapping rats was given by Himiona Tikitu, of Ngati-Awa : — Takii turupou nei Ko whakaihi nukii. ko whakaihi langi Ka poua nei e au Ki runga ki a Papa-tiianuku E whakamau atu ana Ki te tiipua, ki te tawhito. Pona te pou, tu te rupe Ko te ]iou na wai ? Ko te pou na Toi. Ko te rupe na wai ? Ko te rupe na Toi. Toi i hea ? Toi i hekeheke iho i a Maui-mua Poua te pou, tu te rupe Te Pu, te More, te Weu, te Aka. te Rea Tuia a uta, tuia a tai Poua te pou, tu te rupe Kokoia i raro i a Papa-tuanuku Ki a tutangatanga. Nau mai ki roto Poua te pou. tu te rupe Kokoia i raro i a Tane-mahuta I te wao kia tutangatanga 252 Transactions. Nau mai ki roto Poua te pou. tu te rupe Kaiihou ariki tii hokai rangi Tiiia i runga i te ara o Tane Ko Pipiri te ara i heke ai Ki raro ki Tauwhaiti Tuia i raro i te ara o Tangaroa i uta Ko Pipiri te ara i heke ai Ki Tauwhaiti Tuia ra. tuia ra ! This is said to have been a charm used by Toi, after whom Te Whaiti- nui-a-Toi was named. The turupou mentioned was, says Tikitu, a staff made of greenstone, that was handed down from one generation to another, to Haeana and others. As to the method of cooking the native rat in former times, they seem to have been either roasted, steamed, or potted in their own fat. The Natives say, " Ka tunua huruhurutia te More'' — by which I understand that they were roasted with the skin and fur on.* When cooked in the hangi, or steam-oven, it was by the IvpaH process, as the kol-opu fish are cooked. Leaves of the pororua plant were wrapped round the rat, which was then cooked in the oven, the leaves being also eaten. Fronds of the petipeti fern were sometimes used as a wrapper (kopahi) in cooking rats or birds from which the bones had been taken away. Te Puia said, " The native rat was plucked as is a bird, the fur coming off quite easily. The tail, head, and feet Avere taken off, and the bodies were packed in close-woven water- tight baskets, termed poutaka, woven from green flax. These w^ere care- fully lined with fronds of the petipeti fern, and then wath the large leaves of the rangiora shrub, so as to exclude the water. The baskets w^ere then immersed in the waters of a stream. When wanted, the rats were taken out of the basket, placed in a bowl formed of half a calabash, and therein stone-boiled." Rats and birds when potted dowji [in their own fat are alike termed huahua, and these fat foods are often alluded to simply as hinu. To prepare rats for potting they were plucked like birds, which ex- posed a clean, white skin — " me te kiri pakeha " (like a white man's skin), said my informant. The extremities having been cut ofi, the entrails were taken out, and the bones pulled out. The latter process is described as kounu (cf. unu= to draw out). This is not the same process as that of makiri, by means of which the bones are taken out of birds. In the latter case the flesh is cut away from the bones, but in the kounu the bones of the native rat are said to have been pulled out easily without cutting, the flesh appearing not to cling to the bones. The ngakau, or entrails, of the native rat were highly prized as a food item — " the best part of the rat," says an old-timer. They were placed, without any cooking, in calabashes, and so kept until the following spring. They were then eaten with various greens, w'hich come under the generic term of puwha. When the vessel was opened the entrails were no longer recognisable as such, but simply appeared as a mass of fat matter. The rats were placed in a wooden trough, or kumete, and there left for some time, until much of their fat melted and collected in the trough. Stones were then heated in a fire hard by and dropped into this fat, where they were stirred and moved about with sticks, this process being con- tinued until rats and fat were cooked, or sufficiently so to please the Maori * Probably only cooked so when cooks were pressed for time. Best. — Maori Forest Lore. 253 palate. The rats were then put in calabashes, and the hot fat was poured over them. These vessels were then carefully covered and placed in. the food-stores for future use. Paitini says. " Ko te huahua mnnu ka mahia hi te ahi matiti ; ko te kiore o " (A bat flies at twilight, a hokioi by night). Hirorirori. — See Riroriro. Hiivaiwaka. — See Piwakawaka. Horirerire. — See Riroriro. Huia. — Given as Heteralocha acutirostris in the Rev. H. Williams's list.. This bird was never, say my Native informants, a denizen of the Tuhoe district, but of the Ruahine and Tararua Ranges. The long black tail- feathers {kotore huia), tipped with white, are highly prized by Natives as plumes for the hair. Mr. Guthrie Smith, of Tutira, states that he heard of a huia having been shot at Wai-reka, near Te Putere, on the Waiau tributary of the Wairoa River ; but the Rua-tahuna Natives sav that they never heard of the birds- as being found in those parts. Kaeaea (also known as Karearea) (Nesierax novce-zealandice ; Sparrow- hawk). — The male bird is known as kakarapiti. Kaha {Podicipes cristatus ; Crested Grebe). — This bird has long dis- appeared from this district. It was formerly found at the Wai-kare-iti Lake, near Wai-kare Moana. The Natives say that it built its nest on the surface of the waters of the above lake, and anchored the nest to the * Williams queries hakuwai as the great frigate-bird. Best. — Maori Forest Lore. 257 bottom, so that the nest moved with the water but did not drift away. For an illustration of a nest, see " Transactions of the New Zealand In- stitute," vol. ii, page 50, and description thereof at page 74. This bird is said to have the power of remaining a long time under water {he manu ruku roa). (See note under Kamana.) This bird does not seem to have frequented the rivers of this district ; the currents thereof are probably too swift to please it. In vol. iii of this journal Mr. Travers has a paper on the habits of the kaha. Kahu {Circus gouldi ; Hawk). — This bird is still common in this dis- trict. In former times it was sometimes caught by Natives in a trap termed a titara kahu, or tahiti kahu. When Taka-moana, of Te Kareke, was slain at 0-pokere his enemies utilised his liver as a bait for a hawk-trap. Oc- casionally a white hawk was seen in former times, but very rarely. They were called kahu korako (albino hawks), and this term was often applied to a chief. An old saying was, " Me haere i rare i te kahu korako " (Always travel with a white hawk) ; to which the following is sometimes added : " kia kai ai koe i te kai, kia whiwhi i te taonga " (that you may fare well and receive presents). When a chief visited a hamlet he was regaled on the best food, and often received presents, his companions coming in for a share of the good fare. John White has a singular remark at page 65, vol. ii, of his " Ancient History of the Maori " : " The kahu was a child of Mahuika, and a god of fire : hence the colour of its feathers." Kaka {Nestor meridionalis ; Brown Parrot). — The kah-a and the kereru (pigeon) are looked upon as the two most important of forest birds by the Maori, inasmuch as they formed one of their principal food-supplies, being taken in great numbers in former times. The origin or parent of birds in Maori myth is Tane-mataahi. This applies especially to the kereru and koko {tui) birds : while the origin or parent of the kaka was one Tu-mataika ; hence these birds are sometimes spoken of as the " children of Tu-mataika." " Kaore e rikarika te tama a Tu-mataika e rere nei " (How numerous are the children of Tu-mataika flying yonder !) — said of a flock of kaka. The following names are applied to the kaka bird : tarariki, tatarariki, tatariki. These names are applied to the leader of a flock of kaka. Each flock of these birds, say my informants, has a leader, generally a small- sized bird : hence the riki. This bird may also be termed a kaka whaka- taka fokai, or " flock-assembling kaka.'''' This bird keeps on the outer side, or edge, of the flock, and seems to shepherd them — keeps them within bounds, and prevents straggling. It also calls the flock from one whakarua, or feeding-ground, to another, and keeps flying around the outside of the flock. Only one such leader will be found with a flock. A tarariki makes the best of decoy-birds, and is said to be a female bird. Kaka kura : This term is applied to a very rare bird, a kaka that has very brilliant plumage, bright-red feathers — unlike ordinary birds of the species, which are of sombre plumage of a brown colour, not possessing so many showy red feathers. The kaka kura are said not to travel with any flock, but such a bird keeps aloof from others, with the exception of one companion, a bird of ordinary plumage. These kura are very rare : only one such will be found in a district. They are sometimes termed ariki, or leaders. Sometimes two ariki will be found in a district — one kura, or red, and one of white plumage, an albino bird, termed a kaka korako. 9— Trans. 258 Transactions. Albino pigeons are also termed ariki. Koraho ( = white, in the sense of albinism, or of rarity) is an expression often applied to chiefs of the genus homo — as kahu korako, or " white hawk." Tawaka and Tata-apopo. — The term tawaka is said to be applied to a large kaka. If it has a very large head it is a tata-apopo. The tata-apopo makes the best decoy-bird for the pae method of taking these parrots, while the tarariki makes the best decoy for the tutu system — of which more anon. The tata-apopo is said to be the male bird, and is known by the large size of its head. Flock names : A flock of kaka when flying is termed a pokai kaka, but when settled on a feeding-ground is known as a ivhakarua kaka; though the expression ivJiakama seems to mean, primarily, a place occupied or resorted to by a flock of birds — their feeding-ground, in fact. A flock of pigeons (kereru) is alluded to as a tipapa kereru. The word tipapa seems to = whakapapa. A rakau tipapa implies a tree much resorted to by these birds, and on which they are snared. A flock of koko birds when flying is termed a iviri koko, but when settled on a feeding-ground is called a hapua koko. This word kapua, like whakarua, means a hollow, and was probably first applied to a feeding-ground. A flock of ducks {par era) is termed a kawai par era. Ta is another flock- name, but I have only heard it applied to the tataeto (whitehead) and kokako (crow), as a ta tataeto and a ta kokako. In the season known as whaturua, or midwinter, many kaka become so fat that it is difficult for them to take flight — they cannot rise in flight from the ground. When found feeding on the ground they walk to the nearest tree and climb up it— walk up, in fact — and are then caught by hand. When in this state of excessive fatness they are called keketoi by some tribes. The cry of the kaka is extremely harsh, but it also emits a deep whistle at times. The screeching sound made by this bird when on the feeding- grounds grates upon the ear, but when flying their cry seems more to re- semble a croak. This is often heard in the dead of night and at daybreak by us denizens of the realm of Tane. Like most other native birds, the kaka is becoming scarce, but appeared in considerable numbers at Rua- tahuna four years ago, where, near my camp, a single Native shot about four hundred. The kaka utters a peculiar cry or screech when alarmed, the cry being known as tarakeha among the Natives — ka tarakeha te kaka. A similar w^ord is kareha ( = to cry out in alarm), of a kaka bird ; and kaiewha has a similar meaning, as also has the term koriwhai. " Ka kite te kaka i te kaeaea, ka koriivhai.^' All these expressions denote tangi mataku — fear or alarm cries of the kaka. Tarahae expresses the quarrelling of birds — the querulous or angry sounds emitted by birds when apparently squabbling over food. Kaka- tarahae is a place-name. Tarawhete means to chatter or mutter aimlessly — said to have been originally applied to sounds made by the kaka, as when sitting on a perch, but now used to denote the gossiping of persons. Ko- whete has a similar meaning. Kaka were often kept in captivity by the Natives, and used as decoys in the fowling season. Such birds while kept at the hamlet were termed mokai or maitnoa (pets), but when taken to the forest to be used as decoys were known as timori, tirore, &c. Best. — Maori Forest Lore. 259 Tamati Ranapiri, of Ngati-Raukawa, says, " While a tame or captive haka was kept at the village it was simply called a mohai haka, but when taken to the forest and used as a decoy it was termed a timori " : which amounts to saying that a tame bird was called a pet or captive at home, but when used as a decoy was so described. The tirore was a Tcaka used as a decoy, but it was not a tame or captive bird. When commencing a day's snaring the first haka caught would be used as a decoy. This bird was called a tirore, but it was not a maimoa (pet) or mokai (captive). The fowler would make a perch for this bird above his head where he was perched in the tree-top, by lashing a piece of aha or climbing-plant stem to two branches. To this the captured bird was tied by a string secured to his leg. But first the fowler would break the beak of the bird, so that it could not gnaw the cord and so free itself. This bird would attract others by its cries and actions. If other kaka do not come readily, then the hapless tirore is again brutally treated, for the fowler will break one of its wings, tear out a piece of the bone, and give it to the bird. The bird will clutch the bone in its claws, and gnaw at it, making sounds peculiar to it when eating. This attracts other birds, and they hover round, and some settle on the snare-perches and are caught. These decoys are used in a similar way in the fae method of taking birds. The decoy that is placed above the head of the fowler is never taken home or eaten, because it has a certain amount of ta/pu pertaining to it, having been near the sacred head of man. That bird is left to perish miserably in the woods. The tirore is sometimes known as a tionga. The decoy- birds kept at a village were kept fastened to a whata kaka. This was made by placing a wooden trough on the top of two posts, over which a roof was put. In the sides of the trough were made holes, into which were thrust the ends of hardwood rods, about 1 in. in diameter, termed hoka. These hoka were about 6 ft. long, and formed perches for the captive birds, or mokai kaka. Food for the birds is placed in the waka, or trough. If the birds fall to quarrelling, then the old ones are each given their food in a small netted bag, made of fiax-fibre, and termed a rohe, which is secured to the hoka. The birds are secured to the perch by means of a cord fastened to one leg. A bone ring (often made of human bone), often carved, and termed a moria {poria among other tribes), was placed on the bird's leg. On one side it had a hole bored through it, where the cord was attached. Occa- sionally these moria were made by plaiting the epidermis of the midrib of the leaves of the toi, or Cordyline indivisa. I lately came across the follow- ing in one of the innumerable songs of the poet Piki : — E koro, Titi— e ! ' Akuanei au ka whawhati atii ki a koe Tena tonu ra to moria toi Kai to waewae e mau ana mai He tauri komore no te mokai kaka I niahue noa to turutuni. &c. The Maoris often speak of certain stones of a reddish colour which are said to have been often found in the crops of kaka that have reached New Zealand shores from Hawaiki — that is, presumably, from the isles lying north of New Zealand. These stones are known as o manapou. The kaka are said to swallow these stones when they leave foreign parts to fly to these shores. It seems a far cry to hale the kaka of slow, heavy flight from. I seem to have read somewhere that manapou is the name of a Samoan tree. In Mr. J. White's " Ancient History of the Maori " (vol. ii, page 90) we 260 Transactions. find manapau given as the name of a tree of Hawaiki. The very same sentence occurs in Sir George Grey's " Polynesian Mythology." Williams's Dictionary gives " manapau, a tree," and refers it to the latter work. Old Pio, of Ngati-Awa, made a remark to me one day, " There is a lake at Pi- hanga, the green lake. A bird called the manapou is fomid there. It has two topknots on its head. These birds dive to the bottom of the lake in order to bring forth their young. There is also a bird at Rua-M^ahia, the tirotiro, its cry being ' Ti-tiro, ti-tiro!'' " Another old warrior says, " The manatawa is a dark-coloured stone, or kernel, in form like that of the tawa. It is found, like the o manapou, in the crops oi haka that fly hither from Hawaiki, but is somewhat smaller. We believe both to be kernels of tree-fruits of Hawaiki. They are eaten by birds there, and those birds fly here to New Zealand. In olden times the kaka used to fly here in great numbers from Hawaiki, and would be so exhausted on reaching land that they were easily caught by hand." Umanga or umanganui is an expression sometimes applied to birds, more especially to kereru and kaka, as being the two chief species from a Maori point of view. Natives say that the term is derived from unia, the breast, most of the meat on a bird being found on the breast. But umanga- nui is also used in other ways, as Te umanganui o nehe ra, he ivhawhai, the origin of which is not so clear. The kaka nests in hollow trees, as also do the kotare, miromiro, momoutu, niru, and tihe. The young of the kaka were taken from the nest for food purposes when feathers had grown on their wings, but before they could fly. They were not taken before that age. They would be found very fat, especially so were the puta or hollow of the tree a deep one. Paitini says that such a deep hole or hollow in a tree in which kaka nested was termed a rua matini. To ascertain whether or not the young birds were ready for taking, the fowler procured a green branch and rustled it at the mouth of the hole. If very young the birds uttered no cry, but if they squawked on hearing the sound, then the fowler knew that they were old enough to take. Kaka resorted to the same hollow tree year after year for breeding pur- poses, unless they were frightened away by clumsy fowlers. These puta kaka, or breeding-holes, were highly prized. Should a person meddle with one to which he had no right he would be pursued and probably slain. The term matini, or rua matini, is applied, says Paitini, to a deep hole or hollow in a tree (apparently not to a shallow hole). It was in these deep holes that the fattest young kaka were found. Those found in shallow holes, such as could be reached with the arm, were not so fat. In a matini the nest may be at the ground-line, but the opening thereto situated 10 ft. up the trunk of the tree. An implement called a ichakawiri was used where- with to take young kaka from such deep holes. This was a rod or light pole, to one end of which were attached a number of loops of flax or other fibrous leaf. This end was thrust down the hollow into the nest. The young birds, in scrambling about to avoid it, would get mixed up among the loops. The manipulator kept turning the rod round, so that the loops were twisted round the bodies, legs, or wings of the birds, which could then be drawn up. One young bird was always left to " take care of the nest," as the Maori puts it. This was probably done so that the birds would not desert the tree as a nesting-place. Again, if an axe were used on the tree, to enlarge the entrance to the hole or make a new entrance, the birds would desert it. Best. — Maori Forest Lore. 261 W^heu young kaka are taken from these nests and cooked for food, then it is highly essential that the ashes of the fire at which they were cooked should be taken to the tree and cast into the hollow where the nest is situated. If this be not done, then the parent birds will desert that tree and never again nest therein, but will seek and select another hollow tree elsewhere, this new nest being known as a puta tvhaka/piri. For such are the thoughts of the Maori. The kaka is sometimes troubled with a parasite, a kind of worm called ngaio, and when so affected is very thin. The worm sometimes found in the kokopu fish is called by the same name. " He kaka kai uta, he manga kai te moana " (A kaJca on land, a barracouta in the ocean) is an old-time saying, both being famously voracious where food is concerned. Also, the parrot rends wood as the above fish rends a net. The kaka is often found in the forest by the fowler hearing pieces of wood drop from where a parrot is rending a decayed limb in order to get at the grubs therein. " He fakura ki te po, he kaka ki te ngaherehere " (A swamp-hen at night, a, kaka in the forest). These two birds mark, by their cries, the passing of the hours of darkness. ■' He wahine ki te kainga, he kaka ki te ngaherehere " (A woman at home, a parrot in the forest). Another simile. Women and parrots, the two noisiest creatures known to the neolithic Maori. {E tania ! Ko te ahi taica hai whakarite.) It is with much pain that the pakeha transcriber places this saying on record. Nothing but a stern sense of duty enables him to do so. When Maruru hinted to his people that it would be a good thing to slay Tu-te-mahurangi he said, " Ka eke te kaka parakiwai, kaua e takiritia ; ka eke te kaka kura, takiritia'^ (If a common brown parrot mounts the snare-perch, do not snare it, but if a scarlet parrot mounts it, then snare it). By this the people understood that they were to slay the chief, but spare his people. This item is from Colonel Gudgeon's pamphlet on the Ohura evidence. Kakapo (Stringops habroptilus ; Ground-parrot). — This bird is no longer found in the Tuhoe district, but was at one time numerous at certain places, such as the Parahaki lands, on the head-waters of the Waiau River, and at Te Whakatangata, and other such wild, rough forest lands. When some members of the Ngati-Mahanga clan went a-hunting kakapo at the latter place it was a trespassing on the lands of Ngati-Tawhaki, who promptly slew, cooked, and ate the offenders. Kakapo were numerous in former times at Ngatapa, near Manuoha. Their holes were seen in long rows at that place. Natives say that kakapo live together in flocks ; each flock has its own range of feeding-grounds, and its own camp, or whaivharua. Each bird has its own hole (pokorua) at the camping-place. Each flock has its leader, called the tiaka, which is said to be always a small-sized bird. It is called tiaka on account of its smallness (" tiaka = A^m., mother," is the only meaning assigned to this word by Williams). At night the birds come forth from their holes and collect on a common meeting-ground at the whaivharua. This place is a playground for all the birds of that particular ivhaicharua. Having all gathered together, each bird now goes through a singular per- formance, beating its wings on the ground and making a roaring sound, at the same time making a hole in the ground with its beak. The Maori says that these birds collect to tangi. During the above performance the 262 Transactions. tiaka walks round the outer edge of tlie playground, as a sort of sentry. Near morn the tiaka leads the flock back from the feeding-grounds to the common living-place, which is always situated in a rough, steep locality. {Ahakoa he rau nga pokorua, ka kiia tena whenua he whawharun. Ko te mahi a nga kakapo ki te whawharua, he patu i ona paihau ki te whenua, me te rara a tona waha ki te tangi.) I have before me an article on the American grouse, in which the follow- ing occurs : " It is the custom of these birds to prepare their ballroom by beating down the grass with their wings, and then to dance something suspiciously like the "lancers." By twos and fours they advance, bowing their heads and drooping their wings ; then they recede and then advance again, and turn on their toes, swelling their feathers and clucking gently." As to the tiaka, or sentinel-bird, a note at page 192, " Journal of the Polynesian Society," vol. ii, says, " These birds when feeding placed one of their number as a sentinel, which hung by its beak to the branches of a tree, uttering a warning cry." This double performance, doubtless a some- what difficult one, does not seem to have been performed by the kakapo of Tuhoeland. The Natives hunted the kakapo (as also the kiwi) at night, with dogs. Kakara, or rattles, were tied on the necks of the dogs, and the hunters followed the sound of these. They would be careful to approach the whawharua on the opposite side to that from which the wind was blowing. When the birds were assembled, and began their dance, elevating their wings preparatory to striking them on the ground, it is said that they could be caught by hand. But it was necessary to catch the tiaka (leader and sentinel) first, then the others could be easily caught. If the leader was not so caught, then all would escape. The lure-call used when hunting these birds was made by placing the hand at the side of the movith. Kakapo are said to collect berries of the hinau and tawa trees, and also fern-root (aruhe), in the fall of the year, and carry such food to secluded pools of water, in which they place it to preserve it for future use. When summer begins the birds commence to feed on these stores of food. The kakapo, kiwi, kaka, kereru, koko, and weka were all preserved in their own fat in former times, and so kept for future use. In former times cloaks were made of kakapo, the skin being stripped off, with feathers adhering to it, for this purpose. Such garments were known as kahu kakapo. Old Pio, in his quaint way, says, " This is another remark ^ — a different subject: a kakapo. This ancestor was like a bird in appearance : it had two wings. It was a bird of high rank. The feathers and skin were stripped off to make garments for chiefs. Then it would be said, ' So-and-so has a kakapo cloak.' " Kakariki ; syn., Kakawariki and Porete {Cynanorhawphus novce-zea- landicB ; Green Parrakeet). — This bird is generally termed porete by the Tuhoe people. These birds were formerly very numerous, and appeared in flocks about clearings and on the edges of forests, very much as the pihi- pihi, or silver-eye, is now seen. " The origin or parent of the parrakeet," says old Pio, " was one Hine- porete. Her descendants are the kakariki, whose cry is ' Torete, kaurehe ! Torete, kaurehe ! ' The Maori people slay these birds in the autumn by erecting a tanga, and using a lure-call to attract the birds. Now, there was an ancestor named Tutunui (or Tunui), who planted a crop of kumara (sweet potatoes) on the land of Hine-porete and her folk. When the kumara grew above ground those porete folk came and pulled up the whole crop. Tutu- nui observed the loss of his crop, and so he fixed a kapakapa (1) and caught Best. — Maori Forest Lore. 263 and slew all those folk, except Hine-porete, who flew up on to a tree, a mata. She cast her weapon, a patu mata, and killed Tutunui, thus avenging the death of her offspring." Which ends this story. There were three methods of taking the parrakeet — viz., the koputa, the tanga kalcariki, and the puaka. The koputa : A rough shed was built at the edge of a forest. Saplings or branches were used, butt ends stuck in the ground, the tops bent over and tied together to form a roof. Branchlets, fern-fronds, &c., used to cover the framework. The front of the shed was left open. Inside the sheds kurupae or perches were placed for the birds to settle on. These perches were placed near the back of the shed. Pegs or short stakes (turu- turu) were stuck in the ground near the perches, and to these pegs were secured maimoa porete, or decoy-birds, to attract the flock. These decoys do not seem to have been kept at the hamlet, as were kaka, but each trip a fowler would first procure a few birds for this purpose by means of the lure-call. The fowler procures some fronds of paraharaha, a fern, which he carefully arranges in a certain manner and ties to the end of a long stick. Upon seeing a flock of parrakeets {pokai porete) in the distance, he takes the above pole and waves it about, which actions attract the flock, and it soon settles upon trees near the shed. The fowler then conceals himself just outside and near the back of the shed. He lures the porete by placing the side of his hand to his mouth and imitating the peculiar jerky sounds made by these birds when flitting from tree to tree. The birds soon begin to enter the shed and settle upon the perches, where they intently watch the decoy-birds, which are on the pegs in front of and a little below the level of the perches. The fowler has by his side a number of short sticks, each with a reti, or running noose, attached to one end. When he sees that a number of birds have settled on the perches, the fowler takes up one of the sticks, thrusts it through the frail wall of the shed, and slips the noose over the head of a bird. He recovers arms, secures bird, and takes up another stick, until all are used. He then disengages the nooses, sets them anew, and continues his snaring. Kaka were sometimes taken by means of the tari, or noose fixed on a rod. Tanga porete, or tanga kalcariki : This is sometimes termed the pae method, but differs from the pae used in taking kaka, koko, &c., and is like that used in taking the pihipihi. Two upright poles are stuck firmly in the 1. Poi'. Tanga Pokete. 2. Bongohua. 3. Cord, tuu maimoa. earth, and to these a horizontal cross-rod is lashed. This serves as a perch for the birds, and is termed a rongohua. Underneath the cross-piece a cord is stretched across and tied to the pou, or uprights. Several porete are so tied to this string that they can struggle to free themselves, and by so struggling, and flapping their wings, attract the free birds. Thus they serve as decoys, and soon the birds begin to alight upon the rongohua. The 264 Transactions. fowler is half-concealed by a rude shelter of branches or fronds of tree-ferns erected near one of the uprights. He uses a striking-stick or rod, termed a hauhau manu, to strike down the birds with. He makes a swift strike, running the striker along the perch, thus knocking off any bird that happens to be sitting on it. The blow is downward. The rod is usually a light, slight mapau. The puaka : A 'puaka trap is made by making a sort of enclosure of an oblong form, and several feet in length, by sticking a number of rods in the ground in a vertical position. Small rods about 3 ft. in length are used. In this fence-like structure four, six, or eight spaces are left for the birds to enter by. In each space a loop snare is set. Before this trap was con- structed, some food would be placed on the spot several times as bait, to get the birds into the habit of coming to the place. The -pihere was also taken in this manner. A stronger form of the above trap is used for taking hiivi, a tahiti like the tahiti hiore being set at each entrance. The crop of a bird is called tenga. The same term is applied to goitre in the genus homo. The crop of a porete is very prominent when full of food. This crop is of a white colour inside, and of the usual rough surface. A white sand, apparently of volcanic origin, deposits of which are common in this district, is known by the name of tenga kaJiariki. It is said to resemble the rough inner surface of a parrakeet's crop. " Kakariki e tunua, kakariki e otaina,'" is an old-time saying of the Maori. It seems to have been quoted when food was being prepared in times of serious danger. " Never mind if the food be underdone, let us eat it as it is and get away out of danger." The porete was not a shy bird when in flocks, and was much easier to take than some other species. Kakaruwai ; syn., Pihere. — See latter. Kaniana. — A water-bird. A Taupo name. Perhaps the same as Kaha. Kareke. — Rev. H. W. Williams gives this bird as the marsh-rail {Porzana afpnis). As it is no longer found in this district I could not name it, but, from the description given by Natives, judged it to be a rail. They state that it Avas about the size of a 7noho-patatai, another rail. One Native told me that kareke. tareke, and koutareke are all names for the one bird. Williams gives the two latter as names for the New Zealand quail, for which see his list in the " Journal of the Polynesian Society." The quail was at one time very numerous in some parts, and was taken by means of a net. The kareke has long disappeared from these parts, but nearly all the elder Natives say that it was a swamp-dwelling bird, and also a rnanu tohii. It was a sign of good or bad luck to fowlers who heard the cry of this bird on the right or left hand. One old Native states that the kareke and kareke were the same bird ; that it frequented fern country ; that it was larger than the kukurutoki, and had a different plumage. This sounds like quail. Kaivau (PhaJacrocorax carbo, P. varius, &c.). — Several kinds of shags are known bv this name, of which koau is a variant form. (It is as well to mention right here that I am cribbing all scientific names of birds from the Rev. Williams's list, for which see the " Journal of the Polynesian Society," vol. xv, page 193.) Papu or papua is another shag-name — a large river-haunting species. The young of this bird were eaten by the Natives in former times. They generally roost in large numbers on a dead tree situated on some steep hill_ Best. — Maori Forest Lore. 265 side or cliff overlooking a stream or lake. They will roost on the same tree for many years, leaving it in the morning to go in search of food, and returning to it in the evening. Such a tree, that stood on the banks of the Wai-kohu River in the seventies, was the roost of a flock of about sixty kawau. These shaggeries, being usually situated on cliffs or steep sidelings, are termed pari kawau. Shaggeries were carefully preserved and some- times rahuitia by the owners of the land, and resorted to every year for the purpose of securing the young birds. There was a famous one at 0- whaka-toro, and another, named Whakatangihau, near the 0-karika Stream. Both of these were mentioned in Court by Natives establishing their claim to those lands. Kawau moe roa is a term applied to bird-snares, eel-pots, and such nets as are left in the water (not merely dragged). Apparently these are likened to the " long-slumbering kawau " that sits quietly for hours on a log in a river, but is wide awake when a fish heaves in sight. The nest of this bird is a rough affair. Captain Cook speaks of broiling and eating some shags at Whitianga. " They afforded us an excellent meal," he says. But, after all, what is the matter with a beefsteak, or even stewed pigeon ? And that is all right. A small species of cormorant is known as the kawau tatarariki. These smaller kawau are said to represent or be the form of incarnation of an atua maori termed Waerore. I'^When a shag is about to take flight it stretches out its long neck stiff and straight, and so flies. Hence the saying, " Ka maro te kaki o te kawau " (The neck of the kawau is stiffened), applied to a person or party just about to start on a journey. The expression kawau maro, as applied to several columns of troops joining together to form a solid column for the war-dance, has a similar origin. Kea. — The kea, says Paitini, has disappeared. It was a bird that lived in open country. It was smaller than a kaka, and had a different sort of bill. He mea ahua whero taua manu (Of a brown or reddish colour). Kereru {Hemiphaga novce-zealandice ; Pigeon). — We have not much to say about this well-known bird until we come to describe the methods of taking the three principal food-supply birds — the kereru, kaka, and koko. It is known to most of us that rupe is a kind of emblematical name for the pigeon. The local Natives cannot distinguish the sexes of this bird — at least, they have no names for the two sexes. Occasionally nests of the pigeon are found in this district, but not often. They are mostly found in small trees, and about 10 ft. or 12 ft. from the ground. To find a pigeon's nest is looked upon here as an omen of ill fortune, of death or sore affliction for the finder. It is also an evil omen to hear a pigeon calling at night. He tatai mate tena, he aitua. A tree much frequented by pigeons is termed a rakau tipapa {ti= whaka, a causative prefix). Such a tree is usually a taumatua, for which see post, under " Snaring." When these birds become fat in winter the expression " Kua whaturua te kereru " is heard, meaning that the birds are in good condition, having plenty of fat on the intestines. They get very fat in some seasons when there are plenty of toromiro berries, &c. Both the pigeon and kol;o {tui) are very fond of the berries of the white inaire {maire rau nui), hut do not fatten thereon. They were often snared on those trees. The koko also •eats the berries of the maire roro, but the pigeon never does so. When pigeons are feeding on leaves, as those of the kowhai, puruhi (houhi ongaonya, 266 Transaction a. Plagianihus hetulinus), &c., they get very thin, and the skiu gets covered with a kind of scurf [maihi). In some districts the pigeon is called huhu and kukwpa. " He huhu hi te kainga, he kaka ki te haere " (A pigeon at home, a parrot abroad) is a favourite apophthegm of the Maori. It may be applied either to a person who is dowdy, careless of personal appearance at home, but who puts on fine feathers when going out, or to a person who is quiet at home but talkative when abroad. Mr. J. White has preserved (" Ancient Maori History," vol. ii, page 78) an old-time myth as to how the pigeon became possessed of wings, and how its legs and beak acquired their red colour. I have seen but one specimen of an albino pigeon in this district : it was shot at Tarapounamu some years ago by Mr. C. Anderson. The jjlumage, however, was not white, but had a pale pink tinge. Kiwi {Afteryx). — This bird is still fairly numerous in some parts of Tuhoeland. At Parahaki and about Tara-pounamu they are common, though, of course, not often seen. When camped at Hei-pipi, near the latter place, their cries were often heard at night in winter, especially so on wet nights. Several were killed by us, and I noted that the fat seemed to be confined to a layer under and adhering to the skin, the rest of the bird being quite thin. The skin is very thick. One good skin I intended to preserve, but old Tutaka, who was camped with me at the time, came across it, and promptly roasted it at a fire and ate it. He rejected the larger feathers. Kiwi are rare or unknown in some parts of this district. I have only heard one near Rua-toki. As observed, kiwi were sometimes caught with a tahiti, but the usual method of taking them was to hunt them with dogs at night. Kakapo were hunted in the same manner. This seems to have been about the only useful work that the native dog was capable of. The dogs were taken after dark to a place frequented by kiwi, and a lure-call was often employed by the hunters to cause the birds to reply thereto. The dogs were released to find, pursue, and catch the birds, but a kind of rattle was fastened to the dog's collar so that the huntei-s might be able to follow the sound thereof. A dog-collar was made from flax-fibre. When tied up, a stick, called a potete, was secured to the collar at one end, and had a cord attached to the other end by which to tie the creature up. The dogs tried to free themselves by gnawing the stick — hence its use. A muzzle, termed a ponini, was semetimes used on dogs. The rattle, called kakara by Tuhoe, was composed of several pieces of wood {mapara, the resinous heart-wood of the kahikatea tree), or of bone, sometimes whale-bones. These pieces were about 4 in. long, and about four of them were tied to a dog's collar, and rattled when he moved. Major Mair states that these rattles are termed tatara by the Whanganui Natives, and rore at Wai-kato. The word ivhakangangahu seems to define the luring of kiwi by means of a call^ — " Me haere ki te whakangangahu kiwi ma tatau." The word whaka- ngau is here only applied to the hunting and taking of pigs with dogs. The deep whistling sound made by a kiwi hunter to cause the birds to answer him, and so disclose their whereabouts, is termed whakahihi. It is one of the sounds known as koroivhiti, in making which the bent finger is placed in the mouth. The former name is applied only to the kiwi lure-call. '■' Ka ivhakahihitia te kiwi e te tangatay Parties of people used to go a-hunting the kiwi in former times. It was- cold work in winter for these bushmen, who possessed but little clothing. Best. — Maori Forest Lore. 267 Hence the death of Moe-tere and her husband among the snows of drear Huiarau. The cry of the female Tiiivi is rendered by the Maori as " Poai, poai ! " and that of the male bird as " Koire, koire ! " or, as some render it, " Hoire ! " The cry of the male bird resembles a deep, hoarse whistle — such a sound as is termed korowhiti. As old Tutaka put it, " Mehemea ka poai, he uwha taua manu. Mehemea ka korowhio, penei me te korowhiti, a he tane tena.'''' If the kiwi hunter has no dog he takes a firebrand along. He then sounds the lure-call above mentioned, which closely resembles the cry of the male bird. If the birds are not together, but roaming about singly, such a lone bird will approach the hunter, attracted by the call. The merry fowler, on seeing the bird approach hun, waves his firebrand vigorously until it bursts into flames, whereupon the kiwi thrusts its beak into the earth, and is easily caught by the hunter. If the birds are roaming in pairs they will not come to the lure-call. The bird is said to be afraid of the fire when it blazes up (perhaps its eyes are dazzled by the bright flame), hence it sticks its beak into the ground so as to shade its eyes. The kiwi makes its nest in holes among roots of trees, or under over- hanging banks, or holes on steep sidelings. Often they are made under the roots of tawai {Fagus) trees. The Maori has an idea that the bird leaves the eggs to hatch themselves and does not sit on them (awhi). This is such a long process (two seasons, some say) that the tree-roots sometimes grow over the egg and prevent the hatching or escape of the young bird. We note a reference to this in a song composed by one Mihi-ki-te-kapua, a prolific song-composer of the early part of the nineteenth century : — Engari te titi e tangi haere ana — e Tail tokoiua rawa raua Tena ko an nei, e manu — e Kai te hua kiwi i mahue i te tawai Ka toro te rakaii kai runga — e Ka hoki mai ki te pao Ka whai iiri ki ahau. Cloaks or capes of kiwi feathers are still made by Tuhoe and some other tribes. The feathers are woven into and securely fastened to a woven flax- fibre garment. These are termed kahu-kiwi. Koekoea {Urodynamis taitensis ; Long-tailed Cuckoo). — This bird and the pipiwharauroa {Chalcococcyx lucidus) were somewhat of a puzzle to the Natives, who never seem to have understood their habit of migrating. Hence the Maoris have cherished two peculiar myths in regard to these birds. One is that they appear from the ground in spring, having buried themselves in the earth or mud in the fall of the year and remained there throughotit the winter ; the other is that these birds are in some way the offspring of the lizard called ngarara-papa. The cry of the koekoea is short, and is rendered by Natives as "Hoi!" It emits a hoarse whistling sound, often heard in the dead of night. This cry may be heard from about the time the manuka blossoms until the white- pine has ceased to shed pollen. The local Natives state that the young of the koekoea and pipiwharauroa are fed by the tataeto (syn., tataihore). The pipiwharauroa appears at Rua-tahuna about the end of October, or early in November. It is also known here as nakonako and whenakonako, on account of the peculiar markings of plumage. The first of this species heard by me at Ruatoki 268 Transactions. ill 1904 was on the 11th October ; but in 1906 I heard one near Whakatane on the 28th September. In 1903 at Rua-tahima the first I heard was on the 15th October. The koekoea appears soon after the nakonako. When an old Native at my camp saw the first koekoea of the season in that locality he said to me, " Kua puta te koekoea, waineku ana te ahua, ara e ahua poko- rehu ana''' — by which he seems to have meant that the plumage of the bird W8S pale or dingy. Possibly it was a young bird, the markings not yet distinct. Both the above species are 'said to deposit their eggs in the nests of the- tataeto (whitehead, Certhiparus albicillus), or tataihore as it is termed at Te Wairoa, Hawke's Bay. The young birds are fed by the tataeto along with its own. The koekoea, it is said, does not eat berries, but lives on insects, lizards, &c. The nakonako also eats insects. The koekoea attacks and eats the young of the koko, and is chased and attacked by the parent koko birds. The former does not show fight, but escapes by swift flight. The koekoea were formerly taken to provide plumes for the head-dresses of the Maori. The tail-feathers were so used. The term koekoea is sometimes applied to lazy, shiftless folk : " E ! kua rite koe hi te koekoea." It fits well a wanderer or vagabond. In an old ivhakatakiri, or song sung while dandling a child, we find the following : — Ko te uri au i te whenakonako, I te koekoea E riro nei ma te tataihore e whangai. A substance known as tnimi koekoea, apparently the excrement of that bird, is eaten by the Natives. It is found on leaves, and is said to be dropped by the bird when flying. It is licked off by the Maori, who says that it has a sweet taste. The cry of the nakonako, or pipiwharauroa, differs from that of the koe- koea, and it also gives different forms of its cry. These are rendered by the Maori as " Kui, kui! Tioro, tioro, tioro/" Another as " Whiti o, whiti a, whiti of'' But its principal cry is given as" Kui, kui, kui ! Whitiwhiti or a ! " When the cry of this bird is heard, then it is known that the summer is near. When the first cuckoo is heard in the spring the Maori children are heard addressing it as follows : " E manu, tena koe ! Kua tae tenei ki te mahana- tanga. Kua puawai nga rakau katoa. Kua pa te kakara ki te ihu o te tangata, Kua puta ano koe ki runga tioro ai, tioro i te tvhitu, tioro i te waru. Me tioro haere ano e koe tenei kupu e whai ake ki te marae o tama ma, o hine ma. Kui, kui, kui I Whitiwhiti ora!''' (0 bird, I greet you! The warm season has now arrived. All trees are blossoming. The fragrance is scented by man. Once more your resounding cry is heard above, sounding in the seventh [month], sounding in the eighth [month]. Go forth and sing the following song o'er the homes of lads and lasses — ' Kui, kui, kui! Whitiwhiti or a ! ') At page 113 of vol. xxxvi of the " Transactions of the New Zealand Institute " may be found a long and interesting paper on the koekoea. The koitareke, or native quail (Coturnix novcB-zealandice), has long dis- appeared from this district. The younger Natives, who have never seen this bird, often confuse its name with that of the kareke, a rail. (See also under " Quail.") Koknko {Glaucopis wilsoni ; Blue- wattled Crow). — This bird is known as honge among the Ngati-Tipa and probably other tribes. It is now very scarce in the Tuhoe district, a few being occasionally seen among the wild Best. — Maori Forest Lore. 269 forest ranges of Parahaki, on the head-waters of the Waiau River, where no man liveth. In former times they were taken by means of a call-leaf by fowlers, but not in great numbers. They were, of course, eaten by these bushmen. The blue wattles of this bird are termed werewere kokako, a name also applied to a blue-coloured fungoid growth that is found growing on trees. Natives say that when a crow sees this blue object he goes and rubs the sides of his head on it. A flock of crows is termed a ta kokako. An old saying is " Te ta kokako a Ira-motumotu " (The crow flock of Ira-motumotu)^whereby hangs a tale. Ira-motumotu was an ancestor of the Tuhoe people, and it fell upon a certain fine night that Ira's wife went a-fishing for the simple kokopu. She brought some home alive in her puivai, or fish-basket. Ira opened the basket and the fish promptly jumped out. Here endeth the first canto. Anon, in days that followed, Ira went a-fowling, and snared some crows, the which he secured alive in a basket and carried home to his wife. He told her to cook them, and she, simple creature, opened the basket, where- upon the crows all escaped, and flew away far beyond all beck and call. She made wild clutches at the escaping birds, but never again did she handle those crows. Hence Ira's ta kokako has passed down the changing genera- tions as a synonym for the unattainable. Again, when Te Whakatohea raided Rua-tahuna they pursued one Manu-ka-tiu with the pious intention of slaying, cooking, and eating him. One who knew Manu's fleetness of foot said, " You will never catch that man. Just think of his name — ' the Soaring Bird.' " One replied, " Ka rere ia ki hea i te ta kokako a Kotikoti " (How may he escape from the crows of Kotikoti ?) However, the Soaring Bird did escape, and warned Rua-tahuna ; hence the night attack on and defeat of Te Whakatohea at Tatahoata, .where their chief, Te Piki, furnished a breakfast for the Child of Tamatea. Anent the origin of the kokako — it was in this wise : In Maori myth both the kokako and the pakura (syn., pukeko) are the offspring or descend- ants of an old-time tipua (supernatural being) known as Wairua-kokako,. or Hine-wairua-kokako. Koko ; syn., Tui {Prosthemadera novcB-zealandice ; Parson-bird). — The origin of this bird was a singular one, according to Maori myth. The koko bird and the inanga fish (under various names) are both said to be the offspring of Rehua (Antares). In one sense the name Rehua is applied to the constellation Scorpio, except the Scorpion's Tail, which is Te Waka o Tama-rereti. For Rehua is often alluded to as a bird. The curved line of stars extending eastward from Antares is one of his wings — the unbroken one, or paihau ora. The other wing of Rehua is broken, as may be seen if you look at the broken line of stars just westward of Antares. This is the paihau tvhati or broken wing of Rehua. Old Pio, of Awa, said, " There is an ancestor roaming across the heavens : it is Rehua. That ancestor is a bird, and has one broken wing and one sound one. His children are the koko bird and the inanga. Those are the offspring of Rehua. The koko bird is with his ancestor Tane {i.e., is a denizen of the forest). This bird provides food for man, the rich huahua, only eaten on important occasions or by chiefs, often kept for ritual and social feasts. You cannot equal huahua as a food ; it is unrivalled." In the mythical story of Rupe we may note that when that hero visited Rehua in the uppermost or tenth heaven Rehua shook the koko birds out of his hair, where they fed upon parasites (kutu), and had them cooked as food for Rupe. 270 Transactions. The above stones are difficult to understand until we note an explanation given by Mr. .Tregear in a very interesting paper on " Polynesian Folk- lore " (Trans. N.Z. Inst., vol. xix, page 490), wherein he states that lehua { = rehua in Maori) is an ancient name for a forest in the Hawaiian dialect. The Tuhoe Tribe have two names for each sex of the koko. The male bird is known as kopurehe and the female bird as kouwka from the time of the flowering of the kotukutuku until the fruiting of the hinau. During the balance of the year the male bird is termed kokouri and the female kokotea (cf. parauri in Tregear's Maori Dictionary). The term kouwha seems to equal uwha, and is applied to female animals and female blossoms or trees. The Natives say that towards the autumn the koko will, in some seasons, wake up in the night and "talk" for a few minutes, and then again be silent. This is said to be a sign of a fruitful season coming — all forest food products will be plentiful. The koko was, apparently, the only bird taught to talk by these Natives, and the only one kept as a pet. The mokai kaka were kept for use. When a bird was caught which it was proposed should be kept and taught to speak, it had a piece of its long tongue cut oft". This bird is a honey-sucker. A famous talking koko kept at the Hei-pipi hamlet years ago was named Tauaiti, after an ancestor of those parts. It was tohia (end of tongue cut off) by Pirimona, of Maunga-pohatu. The bird was then placed in a covered place. Two pieces of supplejack were fixed in the ground as hoops, one at right angles to the other, to serve as a framework. This frame was covered with a mat or old baskets. Food was placed at one end and water at the other end of this structure, and the bird soon learned to find them. After some time the bird would be put in a cage made of thin twigs of manuka. A small opening was left at each end of the cage, and a small wooden trough, sometimes ornamented with carving, was fixed outside the cage, just under the two apertures. Food was placed in one, and water in the other. These cages were hung in the porches of the houses. After the birds had learned to talk they would begin to air their eloquence very early in the morning. Old-time residents of Pori-rua, of forty or more years ago, will remember such a bird, the pro- perty of hale Jimmy Mitchell. That koko was a past-master in the delivery of the Maori tongue. The tongue of a koko, or the ends thereof, are termed puhihi by Natives, a word also used to denote rays of light, as from stars, &c., and also the tail and side streamers of a kite. These ends of the bird's tongue were cut so as to enable the creature to speak distinctly. If they were not so cut, then the bird's enunciation would be very poor. The koko emits some curious sibilant sounds at the end of each " set piece," which sound much like a person spitting. We here give a few^ specimens of these songs or recitations taught to the koko in former times : — He Ako Koko. Kiki tai pari, kiid tai pari Whakataka horohoro ki tua o Maketu Maranga mai — e — u — e. E — u — e Ka ki te tai, ka heke te tai Ka whakarara koa nga tai o te awa He tai tana — e, elie ! ehe ! Kai tiiha ! \^ Best. — Maori Forest Lore. 271 He Ako Koko- . , 1. Uia te niannhiri me ko wai. Uia te manuhiri me ko wai. Ko Tu koe, ko Rongo koe, ko \Miakamau-tarawa. Tahia te wananga — e. Ko INIatiti, ko Matiti-kuia, ko Matiti-aro. 2. Ko Tupato, ko Hikairo, te Kviti, te weia, te rapa, te haua. E, ko Apanui, Apamii — e ! Alau ki te hoe. Tutaki — e ! Man ki te hoe. Ko te hoe nui, ko te hoe roa, ko te hoe na Matatua. Tikina ra, kaua te tai o Pakihi, kai hika mokai ko koe. Moi, moi — e ! Haere mai ! Ehe ! Ehe ! Kai tiiwha ! 3. E ai ana, tataki ana te waha o to puta. Ka riire te wahine — e ! Te wahine takiri tohetohe. e rere tana. Korihi ake te ata. Karangatia, e ! Haere mai ! Haere mai, e te manuhiri tua-rangi. Kaore he kai o te kainga. Kai tawhiti te kai. Moi, moi — e ! Haere mai ! Ehe ! Ehe ! Kai tinvha ! 4. Koka — e ! Tahia te marae. Koka — e ! Me tohutohu tu te kai. Me tohu te rua iti. Me tohu te nia rahi. Koi tae ki te whitu, me te waru. Tukutuku karere ki raro ki te whakahawea na. E ! Haere mai ! E te manuhiri tviarangi. Kaore he kai o te kainga. Kai tawhiti te kai. Moi, moi, e ! Haere mai ! Ehe 1 Ehe! Kai tuwha ! 5. Ko te when, ko te whare. Te whare patahi — e ! Hui te rangiora. E rongo ki waho, e ! Haere mai ! Haere mai ! E te manuhiri tuarangi. Kaore he kai o te kainga. Kai tawhiti te kai. Moi, moi — e ! Haere mai ! E)he ! Ehe ! Kai tuwha. On comparing a number of versions of the above Icoho speeches I find that part 5 is the latter portion of part 1, and should be added thereto. It will be seen that these birds were taught to cry a welcome to visitors, and to give orders that the plaza of the hamlet be swept and made presentable. Tamati Ranapiri, of Ngati-Raukawa, states that Maoris know the sexes of some birds, and can distinguish them — i.e., the haha, kereru, tui (koko), kokomako (syn., rearea, kopara), and huia. He says also that manu tute (quarrelsome birds) and manu tawpua are always males, no matter of what species. Manu tute is a term applied to birds that bully and drive other birds away from a food-bearing tree, as the koko are sometimes seen to drive pigeons away from a tree {tutetute = to jostle). Manu whakakenakena is an expression applied to a bird when it causes its neck-feathers to stand up like a frill, as the koko sometimes does. The Maoris have a belief that when the koko becomes excessively fat, as it sometimes does, it is in the habit of pecking its breast so as to cause much of the surplus fat to exude. I must decline to guarantee the truth of this statement. That the koko is a somewhat strenuous and interfering sort of creature we know well. It has not much use for birds of other species. Some months ago, when ascending a bush-clad hill near my camp I heard a series of angry shrieks and (apparently) shocking oaths, and presently came upon a strange scene. A gentle ruru (morepork owl) was standing on the ground, and a koko was wheeling and making swift dashes at it, and evidently trying to frighten or drive it away by means of these attacks and discordant shrieks. At last the ruru fled down a gully, pursued by its assailant, who again attacked it as it sat on a branch, and the owl again fled. This process was repeated until I got tired of following them, and probably longer. The owl seemed to make no attempt to retaliate or defend itself. 272 Transactions. The skins of the koko (and also those of some other birds) were used as pohoi, or ear-pendants. The skins, with feathers on, but minus heads, wings, and tails, were prepared by inserting a round stick in them, and hanging them up to dry. Thus the skins assumed a cylindrical form. They were suspended from the ears. Besides being potted and steamed in an earth-oven, the koko was often cooked after being wrapped in leaves. A favourite method was roasting before a fire. A green stick with one end cleft, split doAvn the middle, was used as a spit. It was termed a rapa or korapa, whereas an unsplit stick used as a spit is called a kohuki. Five or more koko or other small birds were stuck in the cleft of a korapa, and the spit was stuck in the ground near a fire. When fowlers were counting a day's takings they did not count two koko as a brace, but reckoned two birds as one, or, in some places, three as one. Hence a pu koko, or brace of koko, consisted of four birds, or, in some parts, of six birds. This was on account of their small size. Tahei koko, or snares for taking this bird, were set all over the top branches of trees frequented by them. When visited again by the fowler, he would often find dozens of birds caught on one tree. Then would be heard the saving, " Me te raparapa tuna.'^ So many birds were hanging from the snares that they looked like a lot of eels hung on a stick to dry. Another such simile was applied to pigeons when so caught in large numbers : " Me te rau rangiora " (Like rangiora leaves). In this case the birds are compared to leaves of the rangiora, which are white on the under-side. "■ He koko kai kohe " (A kohe-eating koko). When these birds are feeding on the berries of the kohe tree they become very fat. This saying is applied to a stout person as a simile. He is compared to a koko that has fattened on kohe berries. Both the koko and pigeon eat these berries. " He koko ivhakamoe, ka mate te tangata " (When like a benumbed koko, men perish). Applied to sleepy-headed, lethargic persons who do not keep a good watch at night ; hence they are surprised and slain by enemies. The koko gets so benumbed on frosty nights as to be unable to fly, and is then taken by hand. " Me he korokoro tui " (Like a tui's throat) is said of an eloquent speaker. This is given by Sir George Grey in his " Maori Proverbs." I have not heard it used among Tuhoe. Kotare {Halcyon vagans ; Kingfisher). — The kingfisher is not numerous in the Tuhoe district ; a few are seen, usually on the outskirts of the forest region. I have seen them pecking into dead, half-decayed tree-trunks in order to form their nests. At a place called Te Puta-kotare, at Whiri- naki, these birds used to make holes for nests in a blufl' overlooking a lagoon : hence the place-name. The Natives say that these birds eat lizards, and hence some persons will not use them as food. The young were in former times taken from the nest just before they could fly, and eaten by those who were not too deeply imbued with superstitious dread of consequences. Kotuku {Herodias timoriensis ; White Heron). — This bird is no longer seen in these parts, and seems to have been only occasionally seen in former times : hence the saying, " He kotuku taunga kotahi.''' In olden days the kotuku is said to have frequented a pond or lagoon at Manuoha, a very wild spot and remote, and also the Kaipo Lagoon, which is the source of the Mokau Stream, at W^ai-kare Moana. The plumes of the kotuku were highly prized by the Maori in former times, being used by chiefs for sticking in their hair. These feathers or Best. — Maori Forest Lore. 273 plumes were known by several names, the three kinds used for the above purpose being the ivhaitiri, tatara, and titapu (or rau o titapu). The tatara were the outside plumes. Another Native states that the bird has four of these prized long plumes in each wing : the first one is called a kapu, and the other three are kira. Women were not allowed to wear these plumes : they were only permitted to wear the shorter ones, which had a distinctive name. If a woman were to wear one of the long plumes, all her hair would fall off. Or, as another Native put it, if a man wearing kotuku plumes is sitting among us as we partake of food, no woman may come and join in the meal. If one does so, then all her hair will fall off. But if the plume- wearer takes it out of his hair and lays it down, then women may join in the meal. These hair-shedding episodes must have been truly annoying to the fair sex of neolithic New Zealand. Tutaka states that the titapu was a very tapu object. Perhaps that was why it acted as a depilatory. The aive kotuku are even now much prized. These are very fine and graceful feathers, of delicate texture and appearance, that overlap the tail-feathers of the kotuku. Kukurutoki ; syn., Toetoe, &c. {Sphenoeacus punctatus ; Fern-bird). -^This bird is usually termed toetoe by the Tuhoe Tribe, and kukurutoki by Ngati- Awa. It is seen flitting among the fern (bracken) and about the edges of swamps. Its ordinary cry is rendered by the Maori as " Te, te, te I " but it has other cries which are regarded as tokens of approaching good or bad fortune by Natives. For this bird is a manu tohu. By its cry we can foretell the success or failure of an expedition, or hunting-trip, or kai taonga {muru) raid. If you hear the toetoe cry " Kore ti, kore ti ! " you will not be successful — not at all. That cry is a puhore (token of non- success). But if the cry of that bird is " Toro ki, toro ki, toro ki f Kuri, kuri ! " that is a sign of good luck : you will gain your object. When its cry resembles " Kuri ivhatia I " that is a sign of disaster or death ; while the cry " Kuri ora ! " is a token of life, peace, and prosperity. Matapu. — A large bird, says my informant, of black (or dark-coloured) plumage. It is like a kaivau in appearance, but has a shorter neck. It frequents forest-streams. Matuku [Botnurus pceciloptilus ; Bittern). — Sometimes called matuku- hu-repo, because its peculiar booming cry is heard in swamps. Several auguries are drawn from the cry of this bird. Thus it gives notice of an approaching wet season, when floods are to be many. Old Pio, of Awa, rambles on anent birds in his usual style : " In the tenth month (April) the sun changes its course and returns to the ocean, to his winter wife, Hine-takurua (Winter Maiden). The sun has many descendants out on the ocean. These are Hine-karoro (origin and personifi- cation of the karoro, or black-billed gull), the next born being Hine-tara (the tara, or tern) ; the next is Hine-tore. The last born of that lot was Punga, the origin of lizards. This Punga also had Haere-nui, then Noho- tumutumu (origin of the kawau), then Moe-tahuna (origin of the parera, duck). The next born after Punga was Matuku (origin of the matuku, or bittern). I will speak of this person, of how he makes the booming sound. There are two signs in the call of this bird — it calls to its parents, and also gives certain tokens regarding the months and seasons. This person, the matuku, goes wandering about in the swamp. It sees a hole, and thrusts its beak down into that hole. The food it contains is an eel. The bird thrusts its head down into the mud and seizes the eel. Then the bird gets 274 Transactions out of breath, its fundamental orifice opens and emits a booming sound. Such is the cry of the matuku." The bittern is now scarce in this district, but few are heard. Mimiro. — See Miromiro. Miromiro ; syn., Mimiro, Tarapo {Petroica toitoi ; Pied Tit). — These little birds are still fairly numerous in the forests of Tuhoeland. The sexes are known by their different colours, the male bird having black and white plumage, while that of the female is of a dingy pale (koma) colour. The female bird is called tarapo. There are two items to record in reference to the miromiro. When Maui, the famous hero of Maori myth, went in search of his mother, he reached Paerau, where he found the folk of that place busily engaged in planting their crops. Maui transformed himself into a bird, a miromiro, which biixl perched itself on the whakamarama (crescent-shaped handle) of a ko (digging- implement) and sang a tewha, or planting-song. After divers adventures, Maui assumed the form of a kereru, or pigeon, and finally found his mother. Again, the miromiro bird was often employed to carry love-messages to a sweetheart or absent wife or husband. There was a certain amount of ritual pertaining to this practice. Certain charms, termed iri or atahii, were recited, and it is said that they were very effective. The bird would go forth and find the desired person, however distant, and perch itself on him or her. At once such person would be seized with a great desire to go to the sender of the bird messenger. Runaway wives or husbands were often brought back by such means, the bird being the active medium em- ployed. I am informed that the above statements are quite true — and who am I that I should doubt them ? " Ma te kanohi miromiro " is a saying preserved by Sir George Grey. (It will take a sharp eye to see or find something mentioned — an eye as quick as that of the miromiro.) Missionary Taylor states that the miromiro " generally flies about graves." After having known this bird for nearly fifty years, I have come to the conclusion that it gets along very well when there are no graves handy. Moa. — This creature is no longer met with in the forests of Tuhoeland, I may observe, but it has at one time roamed far and wide over the steep forest ranges of this district. Moa bones have been found near the sum- mit of the Tara-pounamu Range, at an altitude of quite 2,500 ft. above sea-level, and probably 2,700 ft. These were found by road-workmen at the base of a rimu tree, on a steep sideling. A leg-bone was sent to the Auckland Museum. Natives report moa bones as having been seen in caves or rock shelters in the wild forest country at the head of the Tauranga River (called the Waimana by us), and near the summit of Maunga-pohatu — viz., at Nga Whatu-a-maru. A moa skeleton was found in a chasm near Awa- awaroa, at Wai-kare Moana, by Mr. McGrath. Native tradition speaks of the moa having lived on the Poho-kura Block in times long past away, and also of a lone 7noa that lived on the Tawhiu- au Range, at Galatea. Presumably these upland moa were mountaineers, for they certainly roamed in very rough high-lying country. The word moa is often found to occur in place-names, but whether or not these names have any connection with the bird it is now impossible to ascertain : thus, Moa-whara is a place-name on the upper Whakatane River ; Tapuae-moa, a place near Te Teko ; Moa-nui, a place on the Waio- eka River ; Whanga-moa, on the shores of Roto-kawa ; while rau-moa is a plant-name. Best, — Maori Forest Lore. 275 Tradition states that a moa was killed at Whakatane by one Ngaliue, a very early voyager to New Zealand, who returned to the isles of the north. Mr. Percy Smith heard this same tradition repeated by a very old Native of Karotonga. Pio, of Awa, born about 1823, has his little budget of notes concerning the moa : " There were certain folk on this island in ancient times. They were like birds in appearance, and also resembled man in structure. They had two legs, two arms (?), and a head, and a mouth too, but they could not speak. They stood on one leg and held the other up — drawn up. It always kept its mouth open, because it lived on air (or wind). It always stood facing the wind, no matter whence it blew — north wind, south wind, east wind, all were food for those folk. Those creatures had fine plumes, like birds' plumes, that grew under their armpits. These plumes were called rau o piopio, and were worn by chiefs in ancient times. They were also used, together with huia and kotuku plumes, when dressing the hair of a dead chief for the lying-in state. A certain ancestor of ours, whose name was Apa, came across one of those folk on the western side of Pu- tauaki (Mount Edgecumbe). It looked like a man standing there. Apa struck a blow at the leg it was standing on, whereupon the creature kicked Apa so violently with the drawn-up leg that he was hurled over a cliff and killed. Hence that place has since been known as the Takanga-o-Apa. Those folk of that tribe were called moa. I say those folk who stood on one leg and held the other up are lost : our ancestors killed them. Those moa are no longer seen, but their bones are found — huge bones, like those of cattle or whales in size. They were descendants of Tutunui. They were all slain in ancient times. It was said that sui'vivors of the moa were living on high ranges, on precipitous places, in gullies, at Tawhiuau and elsewhere. I saw some of their bones at the base of Tawhiuau (near Galatea). After Christianity was introduced, a party of Maoris went with a European to search for moa at Tawhiuau. They did not find any." The above, is the only tradition concerning the moa that is known by the Natives of these parts. The ancestor Apa here mentioned flourished about four hundred years ago. The tribe Ngati-Apa, of Putauaki, were apparently of the early inhabitants of New Zealand. The Tuhoe people have preserved no other traditions concerning the moa. Their history, legends, folk-lore, songs, &c., are silent as to the moa, save for the few notes given here. And Tuhoe are truly of the old-time people of New Zealand, who were in camp here long centuries before the last migration of Poly- nesians to these shores. A very singular statement appears at page 494 of vol. vii of the " Trans- actions of the New Zealand Institute." It is quoted from a letter written by the late Judge Maning : " There is no subject, except perhaps the his- tory of their wars and migrations — none on which the traditions of the Maori are so numerous and particular as those regarding the moa," &c. This is somewhat startling w^hen we know that early European settlers and sojoiu-ners in New Zealand could gather but very little information anent the moa from Natives then living, or from song, story, and legend. Colenso is correct in his statement that scarcely anything anent the inoa has been preserved save a few fabulous stories. He made inquiries at Te Whaiti and Te Reinga, and many other places, in 1841, but could gain nothing authentic. The Reinga Natives spoke of a lone moa that lived in a cave (guarded by a reptile) at Whakapunake. They also stated that a few years before Colenso's visit in 1841 they had been raided by the Ure-wera Tribe 276 Transactions. and forced to fly to the rugged Whakapunake Mountain for refuge, and where many of them were slain by the Ure-wera (Tuhoe) raiders ; but they saw no moa in those wilds. Colenso never met with the moa in Maori legend, save in that of Ngahue, given above. He collected nine old-time aphorisms concerning the moa, and a few references in poetry, but very little else. There was no more moa. " Na te moa i takahi te rata " (The moa trampled on the rata), or " He rata te rakau i takahia e te moa," is an old saying that I first heard from Ngati-Hau, of Whanganui. That tree sometimes grows far from upright, and is said to have been forced into that position by a moa treading on it. Sir George Grey has preserved " He mihiau te kohatu i taona ai te moa " (The mihiau stone was used for cooking the moa). The expression moa kai hau, or "air-eating moa," is sometimes met with in poetry, as — Kia noho atu au i konei Hai moa kai hau ki Whakapunake ra. Moho. — Tutaka states that the moho was a flightless forest-bird, but is now extinct ; also that the mohorangi was a flying-bird found in open country, in fern and swamp. Williams gives moho-fatatai as the land- rail {H ifpotcenidia philippensis). The moho-patatai, says Paitini, is a long- legged bird with a small body. It is no longer seen in the Tuhoe district. The last one here seen was caught at Te Whaiti about the year 1890 or 1892. Momotawai. — Given by Williams as the bush- wren {Acanthidositta chloris). I have been told by Natives that momotawai, momoutu, tititipounamu, and toirua are all names for the bush-wren. But others say that the momoutu is smaller than the momotawai, and the latter has disappeared, while the former is still seen ; also, that both are distinct from the toirua and tititi- pounamu. Another ruffian says, " The toirua resembles the momoutu, but is larger, and has no tail. It is the same as momotawai." Te Pouwhare also says that the toirua and momotawai are one and the same bird. The toirua is said to be also known as jnpitori. To take the momoutu the fowler imitates the cry of the bird, and takes a leaf in his fingers, which leaf he shakes and twirls about. This attracts the bird, so that it comes close enough to be caught by hand, even perching on the hand of the operator. Natives say that it mistakes the twirling leaf for its own young. It is a dark-coloured bird. Nakonako. — See under Koekoea. Nonoroheke. — See under Riroriro. Oho ; syn., Oho-mauri. — Given in Williams's list as the land-rail, same as moho-patatai, &c. My Maori notes say : A bird of light-coloured, marked or patterned plumage. A difficult bird to take. It has a habit of appearing suddenly by the roadside as one passes : hence its name, "the startler." Pakura. — See Pukeko. Papango [Fuligula novce-zealandice). — Black teal. Papua or Papu. — A species of kawau (cormorant). Parera {Anas superciliosa ; Grey Duck). — A flock of parera is termed kawai parera when in the water, but pokai parera when flying. When young ducklings take to the water, which they do early in life, they are called kawaiwai. When the parera and ivhio are moulting they are extremely fat, and were in former times caught in large numbers with dogs and even by hand at such times. At other times they were snared. A long cord, Best. — Maori Forest Lore. 277 termed Jcaha, was stretched tightly a little above the surface of the water, being fastened to stakes thrust into the bed of the lake or stream. To this cord were attached innumerable loop snares {tahei, tahere), which were attached to the main cord so as to hang down and bring the open loop just above the surface of the water. In swimming to and fro the ducks were caught by the neck in this running noose. Favourite feeding-grounds of the duck in lakes or wide river-mouths, &c., were sometimes entirely surrounded with a ring line of snares. Maoris do not appear to have been in the habit of taming birds, or keeping them as pets, save in the case of the koko. The kaka were so kept for use as decoys. Occasionally one hears of other birds being tamed, or partially so. For instance, one Tohi-ariki so kept a parera as a mokai or pet, and named it Korotau. On going a journey he left the bird in care of his wife. She neglected to feed it : hence it left the hamlet for pastures new. When Tohi returned he composed the following lament for his lost bird : — Kaore te arolia ki takii nei manu Titoko tomi ake i te ahiahi Ka tomo ki te whare taknate kaix an E whae ma. e ! Tirohia atii nga parera e tere atu ra Ehara tena, he manu maori. Waiho me titiro ki te huruhuni whakairoiro Mai no tawhiti. He rang! an e tatari akuanei He raro an e tatari apopo Kai hea Korotan ka ngaro nei Tena ka riro kai te katokato i te ran pohata Ka whakataiore tn nni ki te po me te ao Ka oho ai an E waiho ana koe hai tiaki hanga Hai korero tana ki tona tanraata Waiho me ui ake te iwi ngaro. Pekapeka (Bat). — The bat is termed a bird by the Maori. They are not often seen in this district. The pekapeka was eaten in former times by the Natives. They usually are foixnd living in hollow trees, and in former times, it is said, large numbers frequented such holes. To take them, a fire was kindled in the hole, and the entrance stopped up in order to prevent the escape of the birds. Thus the birds were stupefied by the smoke, and fell to the bottom of the hollow of the tree, where the merry fowler secured them. These resorts of the bat have a powerful and evil odour. The Natives were careful to kill the first bat caught, as this insured a good bag. If this first one escaped, then but few would be taken. Pihere ; syn., Karuwai, Kakaruwai, Pitoitoi, Tataruwai, Toutouwai {Miro australis : Robin). — This bird was called pitoitoi on account of its cry (which is rendered by the Maori as " Pitoi-toi-toi"), and karuwai (watery eye) because small drops of water are seen exuding from its eyes. Ngati- Awa and other tribes call these birds pitoitoi ; Tuhoe style them pihere ; while Ngati-Kahungunu, of Te Wairoa, use the name karuivai. Tuhoe call the female of this species mokora. The robins practically disappeared from the forests of Tuhoeland years ago, and were rarely seen, though numerous in pre-European days. But in the summer of 1901-2 they reappeared in limited numbers at Rua- tahuna, as also did the rearea, or bell-bird. Mr. R. C. L. Reay, surveyor, writing from Wai-maha, east of Maunga-pohatu, in 1903, stated, " The 278 Transactions. piloitoi are numerous in the Hangaroa district. They come near our camp, and follow along the survey-lines we cut. They appear to be darker in plumage than the pitoitoi I remember north of Auckland many years ago, and without the white lumps at base of beak." When in going hunting or fowling in the forest you hear the cry of the pitoitoi far in the forest-depths, that is a sign of non-success : your trip will be a failure. The pihere is taken by means of a trap termed a horapa, or wTiakarapa. To make this trap a piece of supplejack is bent so as to assume a U shape. Across the two ends a stick is lashed so as to cause the supplejack to retain its shape. It is now like a capital U with a closed top. Dried strips of flax are netted on this frame so as to form a net with a mesh small enough to hold such small birds as the miromiro. The trap now resembles an enlarged section of a snow-shoe — not the ski, but the Canadian snow-shoe. The straight cross-piece is termed a hurupae, and its ends project a few inches on either side of the trap. The trap is placed in a vertical position on the ground, the hurupae resting thereon. Two pegs are thrust in an oblique manner into the ground just above and resting on the projecting ends of the kurupae, and on that side of it on which the trapper takes his stand. The trap will probably be held in an upright position by the pegs ; if not, then a slight stick will be used to prop it up. A cord some 30 ft-, in length is attached by one end to the top of the frame of the trap. This cord is passed through a small hoop of supplejack, like a diminutive croquet- hoop, fixed in the ground just in front of the trap. The cord is carried on to the fowler's stand, he holding the end in one hand. In the other hand he holds a stick, with which he keeps striking a block of wood lying on the ground by his side. This tapping attracts the birds. The Natives say that the birds think it to be caused by some person chopping grubs {huhu) from a decayed tree, a common practice in Maoriland. It is a fact that the robins will collect around persons working in the bush, as I know full well, having often watched and fed them under such circumstances. A bait of berries, earthworms, or huhu grubs is placed on the ground immediately in front of the standing trap, and close to it, so that the trap covers it when it falls. The birds, attracted by the tapping sound, draw near, and soon espy the bait and flock to it. When many are collected round the bait the fowler pulls the cord, which causes the trap to fall upon the birds and thus imprisons them. The cord, being passed under the little horowhiti, or hoop, holds the trap down close and prevents the birds escaping. All the fowler has to do is to retain his strain on the cord when he advances to secure the birds. Other small birds, such as miromiro, &c., are taken at the same time. It is not the pihere alone that is attracted and so taken. No bird is too small to serve as food for the Maori, as witness the taking of the pihipihi. Pihipihi ; sy n., Karu-patene {Zoster ops ccerulescens ; Blight-bird, Silver- eye). — This bird appeared in this district before there was any fighting with Europeans in Tuhoeland. It was known here at first as karu-patene (? button-eye). This bird is taken in great numbers in the Rua-tahuna district by the call-leaf and striking process, exactly similar to that method of taking parrakeets termed tanga porete and tanga kakariki, for which see under Kakariki. The decoy pihipihi are tied by the beak to the cross-cord with a short string. The fluttering and struggles to escape attract other birds, which perch on the cross-rod, and are struck down by the fowler, who Best. — Maori Forest Lore. 279 is half-concealed within a shelter of branches or fern-fronds. A call- leaf is also used by fowlers. These birds are preserved in fat in great numbers in the interior of Tuhoeland. They are not carefully plucked — many feathers are left on — and they are not cleaned. But that matters not. The hardy Tuhoean bush-folk crunch up the birds — head, bones, inside, remaining feathers, and all — with great zest. But the pakeha looketh sideways at this delicacy. Piopio ; syn., Koropio {Turnagra tanagra ; North Island Thrush). — The North Island thrush is almost gone from the forests of Tuhoeland. There are said to be some still in the Parahaki district, a wild uninhabited tract of rough forest country but seldom visited by Natives, and which but few Europeans have penetrated. These birds are said to have been numerous in former times all over the Tuhoe district, and fowlers used to take them in considerable numbers, attracting them by means of a lure-call. A leaf was generally used whereby to make most of these lure-calls. The plumage of this bird is described by Natives as pakaJca, or ivhero popouri, in regard to colour. (See Pohowera.) Pipitori. — Said to be another alias of the toirua. Pipiwharauroa. — See under Koekoea. Pitoitoi. — See Pihere. Piwaiwaka ; syn., Tiwaiwaka, Piwakawaka, Tiwakawaka, Tirakaraka, Hirairaka (Pied Fantail). — This is the bird that caused the death of Maui, the hero who endeavoured to gain eternal life for man, and failed at the task, as many others have. In this and some other myths birds are alluded to as Te Tini o te Hakuturi, though it would sometimes appear that the term is applied to fairies. In like manner the expression Tini o te Mahoihoi is sometimes explained by Natives as being a sort of general term for birds, though others state that it is applied to plants, &c. Pohowera. — I have heard this name applied to the piopio, but I do not know that it is a genuine name for that bird. Pohoivera is certainly the name of a sea-bird. This bird is also found a certain distance inland at times. If its nest is found in a kumnra cultivation the eggs are carefully counted, for it is, or was, believed that the field will produce twenty baskets of kumara (sweet potatoes) for each egg the nest contains. Porete. — This is the most common name for the parrakeet among the Tuhoe Tribe. (See under Kakariki.) Pukeko ; syn., Pakura {Porphyno melanonotus ; Swamp-hen). — These birds were never numerous in the Tuhoe district, which is essentially a forest country, the realm of Tane. I have not yet seen this bird hereabouts. In former times they were numerous in the Ngati-Awa district, which contains a great area of swamp-lands. They were snared in a similar manner to that employed in taking ducks, except that the apparatus was fixed on land. A long cord was stretched tightly from stake to stake, and from this cord hung many loop snares, at such a height above ground that a pukeko, in walking, w^ould be likely to thrust its head into the loops. The expression kawau moe roa, oi "long-slumbering shag," was applied to all such snares as were so left, unattended by the fowler, for the birds to catch themselves in. It was also applied to eel-pots and all such nets as are left in the water. The pakura, or pukeko, was a troublesome bird to the Maori agriculturalist, for it entered the fields at night and scratched out and ate the tubers of the kumara (sweet potato). As we have seen, the pakura and kokako are sprung from a mythical being known as Hine-wairua-kokako, a tipua, or supernatural being. Say& «? 280 Transactions. Pio, " The pakura are a troublesome folk. They are the offspring ot Hine- wairua-kokako. Most evil are the actions of that ancestress and her off- spring in pulling up and devouring the food of the Maori people. When seen assailing the crops a person goes to hiehie them (to drive them away by shouting at them). This is the ivhakahiehie : — Hie ! Hie ! Haere ki te huhi Haere ki te repo Haere ki a Hine-wairua-kokako. Hie ! Hie ! Haere ki a Hine-wairua-kokako Hie! Hie! The sign by which the Maori kriows the approach of daylight comes from the pahura. Its cry is heard about midnight, again later on, and again a third time. The third cry tells us that daylight is at hand." Quail. — The New Zealand quail was known in this district, but disappeared many years ago. It was once numerous in open country, and was taken with nets. It is Coturnix novce-zealandice. The Native names of the quail given by Williams are koreke, koikoiareke, koitareke, kokoreke, koutareke, and tareke. Bearea ; syn., Korimako, Korihimako, Kopara, Kokomako, Kokorimako (Anthornis melanura ; Bell-bird). — The rearea was sometimes speared, and also taken by means of a puaka, which is an enclosure made by thrusting sticks or branches into the ground so as to form a sort of fence. Small openings were left by which the birds entered to eat the bait placed inside. Loop snares were arranged in these open spaces, by which the birds were caught. The porete was also taken in this manner. The bell-bird had long disappeared from Rua-tahuna when I first visited those sylvan wilds in 1895, but reappeared there in the summer of 1901-2. I often heard them near my camp in that year ; but they were not numerous. It was not like the delightful clamour heard in the bush of the Wellington District in the early sixties : that was something to remember. Riroriro ; syn., Nonowheke, Nonowheko, Horirerire, Hirorirori, Korire- rire, Totororire {Totorori ?) {Pseudogerygone igata ; Grey Warbler). — This is a manu toJiu tau of the Maori. It shows them what the coming season will be bv its manner of building its nest. If its snug little roofed nest is built with the side entrance thereto facing the north, then the prevailing wind of the coming season will blow from the south, and vice versa. If the Oldening of the nest faces the muri wind a tau tokerau will follow — that is, easterly winds will prevail, and it will be a pleasant, prolific season. If the nest faces the east, that means a tau hauauru, he upoko maro — a westerly and cold, inclement season : crops and forest products will not be satis- factory. The muri is a wind that blows from the coast up the Whakatane Valley. This wind betokens good fishing weather. It is styled a hau aroha, a favourable wind. Upoko maro is a term used to denote cold weather — the cold south winds, or to7iga kokoti. The cry of this bird is rendered by the Maori as "Biro, riro, 'rirof' When this cry is heard in winter or early spring it is a sign for man to be up and doing — to commence the work of preparing cultivations for crops, &c. It is urging the Maori people to commence the work of the year. Two authorities give me totorori as a name of the riroriro. Another Native says it was a bird similar in size and appearance to the riroriro, but not the same ; that it was a forest bird, but is no longer seen. Best. — Maori Forest Lore. 281 Ruru [Ninox novce-zealandice ; Morepork). — This well-known bird is some- times known as Jcoukou and peho. As Mihi-ki-te-kapua of old sang, when left lonely in her old age at Wai-kare Moana, — • E peho, e te nini, he tokoiua ano Tena ko au nei, he kotahi. If a ruru is heard to utter its cry at a junction of two tracks it is looked upon as a sign that a hostile party is approaching — a war-party is at hand — look out for squalls. As old Pio put it, " I begin another subject — the warn- ing given by the ruru when danger is nigh. If a war-party approaches a hamlet, this bird gives warning of its coming. It calls out to the people of the place in this way : ' Kou, kou ! Whero, whero, tvhero ! ' Then the people arise and fly to the forest. The enemy assaults an empty place." So much for the wise owl. A Native states that the morepork has four different calls, and that if a person imitates the bird's cry it will answer him. Its first cry is " Kou, kou ! " hence the bird is in some places termed koukou — an example of onomatopoeia. The next cry is " E — e — e ! " which is he tangi aroka ki te tanxjnta — a kindly greeting to man. Another cry is " Whe. u'he, toJie ! " and then " Peho, peho ! " which latter is thought to betoken anger. Pio, of Awa, says that the bird will answer a mimic call three or four times : " Ko te ruru, tana korero, kou, kou ! Ka utua e te tangata, ka tahi pona, kou, kou ! Ka rua pona, kou, kou ! Ka torn pona, ka vhakarere. Ka wha pona ranei, ka whakarere.^' These birds were, and are still, eaten by Natives. They are simply knocked down with a stick, or snared by means of a slip-noose on the end of a stick. The fowler takes a leaf between the thumb and one finger of his left hand, and twirls it in order to attract the attention of the bird as he slips the noose over its head. Native children will cook and eat a morepork, or any other bird, wherever they happen to kill one. I have a friendly ruru at my camp here, beneath the frowning defences of the old Hau-kapua pa. On cold winter mornings, when the frost is keen, this bird comes forth from the bush as soon as the sun rises, and perches himself upon my garden-fence, where, with closed eyes, he suns himself for an hour or more. Though very close to the camp he does not get alarmed, knowing by experience that he will not be molested. In only one case have I heard of a ruru being looked upon as the form of incarnation of an atua maori. Karukaru, an atua or demon of the Natives of the Whanganui River, was brought to this district some years ago {i.e., his cult was so brought, I presume). The aria of Karukaru is a ruru. This was the familiar demon of Matoru, a would-be shaman of these parts, whose nose was put out of joint by Rua the keka. This demon, Karukaru, guards his human mediums from danger, warns them when any one is attempting to bewitch them, &c. One evening old Paitini returned to his home at Heipipi and found a ruru perched under the porch of his cabin. The bird was startled and flew away to an open shed, where it perched itself upon a buggy that old Pai had bought. The old man at once suspected something was wrong. A most superstitious man, your elderly Maori. He suspected the poor ruru to be the worthy Matoru's demon, sent for no good purpose. He went to the shaman and made inquiries. Matoru told him that he had sent his familiar demon to take possession of the buggy, which was hence- forward to be the property of the dread Karukaru. Pai was also told that if he did not quietly give up possession of the buggy, then both he and his 282 Transactions. wife would die — that is, be slain by black magic. Hence this couple were much disturbed : they washed neither to die nor yet lose their buggy. At this juncture the godless pakeha stepped in, and, with incisive vocabulary and impious disregard for gods or demons, broke up the game. Tarapo. — Williams gives this as a name of the kakapo. Akuhata te Kaha, of Tuhoe, says it was a forest bird, smaller than a kakapo, and no longer seen. Te Pou-whare states that tarapo was the name of the female miromiro. Tataeto ; syn., Tataeko, Tataihore, Tatangaeko, Popokotea, Tatariheko (Certhiparus alhicapiUus ; Whitehead). — These birds are still seen in the Rua-tahuna district, though not numerous as of yore. I have come across flocks of them in remote places there — or, rather, they have come across me. They move in flocks, flitting quickly from tree to tree. Natives say that the tieke and tike birds join flocks of whiteheads and accompany them ; a few will be seen with each such flock. A flock of whiteheads will some- times set on to a ruru and chase it about, even as the koko does. A flock of whiteheads is termed a ta tataeto by Tuhoe and taki tataeko by Ngati-Awa. Ngati-Kahungunu, of Te Wairoa, call this bird tatai-hore. Tieke {Creadion carunculatus ; .Saddleback). — This bird has entirely dis- appeared from the forests of this district, albeit there are here hundreds of thousands of acres of wild forest lands, within the shades of which man is but seldom seen. The Natives say that bees have destroyed the tieke by occupying the holes and hollow trees where the bird was wont to breed. This is absurd. Such holes and hollow trees are here by the million in this great forest, but bees' hives are scarcer than in any other part of the Island I have camped in. In the fair vale of Whare-kopae, Poverty Bay, I found nine hives within half a mile of my tent. To find one in the Tuhoean forest would need about a day's search. When going a-hunting or fowling, if you hear the cry of a tieke on the right-hand side of the track it is a marie, or token of good luck — you will be successful ; but if you hear it to the left, that is a puhore, or sign of non- success. At Repanga, or Cuvier Isle, there are said to be two tieke birds, named Takereto and Mumuhau, which are atua, or supernatural beings. They are claimed by the migrants of both the " Matatua " and " Arawa " canoes. In taking the tieke — for all forest birds were food for these bushmen — in some cases a fire was kindled. This is said to have attracted the birds. Tike {Pogonornis cincta ; Stitch-bird). — The male bird is termed tihe- wera. Its plumage is described by Natives as being whew manaeka (? yellow- ish-red). The female is called tihe-ioai. This bird disappeared years ago from the forests of this district. It was taken by means of the puaka snare-trap. Titi. — This sea-bird was formerly found in large numbers on the rugged ranges of this district, where they had breeding-places to which they came every year. The Natives used to visit these places every year to take the birds, both young and old. These were preserved in fat in great numbers. They were placed in calabashes by the inland people, but those who had access to the coast used vessels made of a large species of seaweed or kelp. These latter vesssels were called poha. The advent of the Norway rat put an end to this food-supply, for they devoured the young birds ; hence the titi ceased to come to these parts to breed. Places where these birds were taken by fowlers are known as ahi titi {titi fires), because a fire was always kindled on such occasions. The tops Best. — Maori Forest Lore. 283 of cliffs, hills, and ridges seem to have been selected as places whereat to take the titi. A net about 20 ft. or 30 ft. in length was set up on the edge of such cliff or slope. This net was fastened to poles or stakes inserted in the ground. Each pair of stakes was lashed together at the top, thus form- ing an inverted V — so A Where these two stakes crossed and were lashed was termed the mata tauira. The upper rope of the net was called the fama-tane, and the rope on the lower edge the tama-wahine. The net was made of flax-fibre. Old persons, past their hard-working days, spent much of their time in making nets, snares, &c. These birds were taken at night- time, about November. A fire was kindled in front of the net and a little distance from it. Behind the fire, and immediately below the net, the fowlers were seated, each having a short stick in his hand wherewith to strike down the witless birds. The birds, attracted by the fire, flew to it, and came into contact with the net. Ere a bird recovered from the shock it was struck down by the fowlers. A foggy or misty night was considered best for taking these birds. Two men only remained standing : their task was to strike down the high-flying birds that flew against the mata tauira. Should the first bird taken chance to fly against the tama tane, or mata tauira, that was looked upon as a sign of poor luck — but few birds would be taken that night ; but should it strike low down the net, at or near the tama wahine, that was an excellent omen — many birds would be taken. If a menstruating woman chanced to be among the party of fowlers a very poor bag was the result — the birds would fly about, screeching loudly, but keep clear of the net. Also, the fowlers were careful not to cause any of the birds to bleed. If any blood were drawn, then no more birds would come near the fire. Great numbers of these birds were taken by such means in former days, before the European rat appeared on the scene. The birds were plucked, cleaned, and the bones taken out ; then they were prepared at the ahi matiti for potting. A large number of places are pointed out here as former ahi titi, mostly on the higher ranges, as those of Huiarau, Maunga-pohatu, &c., and at Wai-kare Moana, 0-tukopeka, Te Rua-ngarara, Taumata-miere, and count- less other places. Titiporangi. — The only note I have anent this bird is, " A forest bird, smaller than a titi. It has disappeared from this district. It was dark- coloured on one side and light-coloured on the other." This is the render- ing of the original Maori. Williams gives titiporangi as a name of the black teal. Tititipo. — This was given me as a bird-name, but more 1 cannot say. Tititipounamu. — See Toirua . Tiivaiwaka, Tiival-aivaka. — See Piivaitvala. Toetoe. — Same as kuJiurutoki. (See latter.) Toirua. — See under 3Iomotawai. Totorori. — See under Riroriro. Totororire. — See under Riroriro. Turi-whekoi-rangi. — A sea-bird. Tuturiwhatu {Ochthodromus obscurus ; Dotterel). — The name of this bird is connected with that of one of the sisters of Taukata — he who brought the knowledge of the kumara to Whakatane. The two brothers, Taukata and Hoaki, had two sisters, Kanioro and Tuturiwhatu. These were the children of Rongoatau, of Hawaiki, and descendants of Pani and Rongomaui. This Tuturiwhatu met with an accident and had her chest burnt. The bird 284 Transactions. of the same name is said to be her, or represent her. It has no place in this list, save the fact that it is sometimes seen on the river-beds of this district. Welca (Wood-hen). — These birds are not numerous in this district, but are said to have been so formerly. In those days they were snared, and also hunted with dogs. Whehau. — See Hakoke. Weweia {Podicipes rufipectus ; Little Grebe). — Natives state that a pair of these birds are always seen in a crateral pond on the summit of Mount Edgecumbe by those who ascend that isolated cone. Whenahonako. — See under Koekoea. Whio [H ynienokemus malacorhynchus ; Blue Mountain-duck). — One often sees these birds when traversing the rough streams of the high-lying in- terior, as at Rua-tahuna. These birds were taken at night, the fowlers carrying torches, which they flashed suddenly on the birds when near to them. This is said to cause the birds to settle, whereupon they are struck down and secured. Whioi {Anthus novce-zealandiw). — Ground-lark. The following is a list of the birds that have disappeared from the Tuhoe district, and several other species may be marked as doubtful, as the kokako, piopio, and others. It must be remembered that nearly the whole of this district is covered with dense forest, with few clearings, and that the Native population is small, and residing principally on the outskirts. Hakuwai. Kea. Moho-patalai Hnkolce, or ivhekau. Koilareke. Moho-rangi. Kaha. Kotuku. Momotaicai. Kakapo. Moa. Tieke. Kareke. Moho. Tike. Cutting out the hakuwai and nioa, we have here a list of thirteen species that have disappeared from this district since the coming of Europeans to these isles, whilst some others have almost, if not quite, disappeared. The species that have survived have almost all become greatly reduced in numbers. The koroire is said to have been a water-bird, a species of duck. Mr. C. E. Nelson tells me that he got the name from an old Native of Ngati- Whatua, who had seen it in his youth. It has not been seen for many years. This was the origin of the place-name 0-koroire. We will now endeavour to explain the Native theory or belief as to the cause of the disappearance of native birds — for they firmly believe that it is primarily due to certain ancient customs and faiths having been abandoned by themselves, the Maori people of these isles. They believe that the de- generation of the Maori, and the serious lessening of the Native population, have been brought about by their forsaking ancient customs and old-time cults — by their having become noa, or free from tapu — debased, in fact — through contact with Europeans. And they hold a very similar belief in regard to the cause of the disappearance of birds, or the lessening of their numbers. The old-time Maori was, or believed himself to be, an extremely tapu person. His system was, as it were, imbued or permeated with a highly sacred, semi-volatile, and all-pervading non-material ichor, a spiritual and intellectual essence or ether. And it was this that preserved man from death or disaster of certain kinds. When speaking of a person's hau or kawa ora, it is this that is in the speaker's mind. It is the tnauri ora of Best. — Maori Forest Lore. 285 man. Even land possesses this quality, as we shall see anon. It is the very essence of vitality. If lost or debased in any way, the person, or tree, or forest, or land is in a truly bad way, and armourless against shafts of magic or other evil influences. Broadly speaking, the above state may be termed tapu; but there are many inner terms and definitions which cannot be understood by the pakeha. Said Ngahooro te Amo, of Ngati-Mahanga. " Birds were exceedingly numerous in former times, before Europeans came. In the days of my youth, at Te Whaiti, when the multitude of birds were singing in the early morn, a person's voice could scarce be heard in the forest, so great was the noise. Birds were numerous so long as we cooked them in the ancient manner — that is, in a hangi (steam-oven) ; but when we began to cook them in the kohua (iron pots) obtained from Europeans, then it was that the evils of the tmvhanarua came upon us. For it was unlucky and of evil omen. Then it was that birds began to decrease in numbers." The word tawhanarua means '' to cook a second time." When cooking birds, should they be found to be underdone when the oven was opened, then the proper thing to do was to use them in that state, and not attempt to recook them. If they were cooked again, then the birds of the adjacent forest would surely disappear. So sayeth the Maori. Said Himiona Tikitu to the writer, " In olden times birds were always cooked in the evening. If cooked in the daytime, then all birds would desert the forest. They would be heard flying away in myriads in the night-time, migrating to other parts. The tawhanarua or tao rua (second cooking) would have the same effect, as also would the use of Euroj)ean cooking-vessels. Because the forest and its denizens became tamaoatia (defiled) by these things. Hence the birds would disappear, even as we Maori people did after we became noa (defiled, free of tapu) by washing in water heated in the cooking-vessels of the white men. But remember that the above restrictions only obtained during the busy part of the bird-taking season — that is, while the birds were being potted down for future use. When this labour was ended, then the above restrictions were removed." In the above remarks we see how the life principle, the vitality, of man, birds, forest, and land were seriously affected and endangered by certain simple acts of omission or commission. The scarcity of birds now so remarkable in this forest district became most marked about the middle eighties, though they had been gradually decreasing in numbers for many years before that time. When forwarding my first contribution of these notes on forest-lore, I remarked that the balance must lie over for another year. Alas for human hopes ! — for there is still a balance, and a bulky one, I ween. Peradveii- ture we may prepare that balance ere the sun again returns to Hinetakurua, the Winter Maiden, and send it forth as an amonga to the modern whare takiura, whose priests are the men of the linotype. It was Kuha-tahi, the husbandman, who cried, " Hoatu, hoatu ! He ra tapahV^ 286 Transactions. Art. XXXIII. — A Contribution to our Knowledge of the Physiological Action of Tutin* By Frank Fitchett, M.D. Edin. [Read before the Otago Institute, 10th November, 1908.] A. Historical. 1. General and descriptive 2. Botany of the tiitii plant 3. Work of jjrevious observers 4. The active principle . . B. Original Work. 1. General action of tutin on mammals — («.) Cats (b.) Rabbits (c.) Gninea-pigs.. 2. Action on birds 3. Action on rejitiles 4. Action on amphibia . . 5. Action on fishes — (a.) General action (b.) Comparison of action of tutin and picrotoxin (c.) Effects of tutin hydrolysed by hydrochloric acid (d.) Action of alkalies on tutin (e.) Influence of " surviving " organs 6. Action on insects 7. Action on larvse 8. Action on molluscs . . 9. Action on infusoria and amoebae 10. Action on putrefactive bacteria 11. Action on yeast 12. Action on germination of seeds 13. Action on tissues — (a.) Action on primitive protoplasm (6.) Ciliated epithelium .. (c.) Action on striped muscle and nerve-terminations 14. Action on the different systems — ■ (r/.) i\limentary system . . (6.) Hoemopoietic system (c.) Circulatory and respiratory systems (d.) Urinary system (e.) Genital system (/.) Nervous system ig.) General nutrition 15. Fate of tutin in the body 16. Imnnmity or tolerance 17. Pharmacological relationship of tutin . . 18. Action of remedies 19. General summary Protocols of experiments Literature references Page. 287 291 293 294 295 298 299 299 304 304 306 309 311 313 314 314 315 315 315 316 316 317 317 317 318 319 320 320 323 323 323 326 327 327 328 329 332 333 365 * Being a thesis presented to the University of Edinburgh, for which the degree of Doctor of Medicine was granted. FiTCHETT. — Physiological Action of Tutin. 287 A. HISTORICAL. 1. General and Descriptive. On the 20th May, 1773, at Queen Charlotte Sound, Captain Cook sent on shore a ewe and a ram which he had brought from the Cape of Good Hope with a view to stocking New Zealand with sheep. On the 22nd he " received the unpleasant intelligence that the ewe and ram which with so much care and trouble he had brought to this place were both of them found dead. It was supposed that they had eaten some poisonous plant, and by this accident all the Captain's hopes of stocking New Zealand with a breed of sheep were instantly blasted " (1). He tried again, however, wnih. goats, but with Uttle better result. Cook's supposition that the flora of New Zealand includes a plant possessing highly toxic properties was well founded. That his ewe and ram shared the fate that has since been meted out to many thousands of sheep and cattle, and to not a few human beings, is in the highest degree probable. The poisonous plant whose existence was suspected in 1773 has long since been identified as a Coriaria, and is known throughout the Dominion by its Maori name tutu, or, as Europeans often pronounce it, " toot." The difficulties met with by Cook in his attempts to stock the country were again encountered by the early settlers. Large numbers of their flocks and herds were destroyed by eating the leaves and succulent young shoots of this attractive shrub, for it abounded everywhere, and grew most profusely where the soil, by its richness, offered an inducement to the pioneer to settle. Animals hungry and in poor condition were particularly prone to succumb to the effects of the poison ; and, as these conditions prevailed with most of the beasts landed from the ships, it will be understood how great an impediment to stocking the country this noxious plant proved. The very first issue of the Lyttelton Times (2) notices the death of three out of five eows that had just been landed — one fell over a cliff, and two others were poisoned by eating tutu. The newspaper, in warning settlers of the danger- ous properties of the plant, says, " It is impossible to take too much care in landing cattle at this place. To beasts just out of a ship the tutu, of which there is abundance here, is certainly fatal." The damage done to stock was enormous, as may be gathered from the following quotation from Dr. Lauder Lindsay's article " On the Toot Plant and Poison of New Zealand " (3) : " In the course of a tour through the New Zealand provinces during the latter part of 1861 and earlier months of 1862 I was everywhere struck by the abundant evidences of devastation produced among flocks and herds from their feeding on the ' toot ' plant, one of the most widely distributed and familiar indigenous shrubs of the country. One settler friend told me of his having lost by ' tooting ' two hundred and fifty sheep ; another, eighty to a hundred sheep of a flock of four hundred ; a third, seven of sixteen bullocks ; a fourth, six of twenty- four cattle ; a fifth, twenty-four cattle ; a sixth, six of eight cattle — each of these instances in a single night. Another flock-master lost four hundred sheep out of a flock of two thousand, twenty-five being frequently dead of a night. In other words, he seemed a fortunate farmer or runholder who had not lost more than 25 per cent., or one-fourth, of his stock from toot poisoning ; while in some instances the losses were so high as 75 per cent., or three-fourths. Some of the colonists had suffered so severely from losses of bullocks by toot poisoning that they were at the trouble and expense 288 Transactions. of attaching a boy to each of their bullock-teams, solely for the purpose of preventing their animals feeding on this pest of the colony. Such inci- dents I found were of daily occurrence. I met few settlers who had not at some period had occasion from this cause to mourn the loss of sheep or bullocks — the former sometimes by the hundred, the latter by the dozen." These remarks of Lindsay serve well to illustrate the deadly nature of the plant, and the embarrassment it offered to the pioneers of the country. They also point to the importance and great desirability of an investigation of the physiological action of the poison being made, in order that the treat- ment of its effects may be conducted on rational lines, and as the first step towards the discovery of an appropriate antidote. But while sheep and cattle have been the chief victims, human beings have not proved exempt, and he was a lucky farmer who lost only his cows or his sheep. Too often one of his children succumbed to the effects of eating the berries or young shoots. Nor is this strange, for the shrub in full fruit is a very striking and attractive object. The numerous racemes of richly coloured, tempting-looking berries — at a glance not unlike black currants — could hardly be overlooked or neglected by the child or thirsty traveller ignorant of their dangerous properties. Numerous cases of poisoning must have occurred, but the recorded deaths from this cause are not many. The following are all that occur in the literature that has been laid under contribution : 1. Thomson (4), in 1859, mentions that up till that date several children had died from eating the berries. 2. Lauder Lindsay (3) mentions the case of twelve French sailors who were poisoned by eating the berry ; four of them died. 3. The Otago Colonist (5) records the death of one of two children in 1861 who had eaten the shoots. 4. The Otago Daily Times notices the death of a young man in 1862 from eating the shoots (6). 5. Easterfield and Aston (7) put on record the following cases : A girl in 1854 55, from eating the berries ; a bov in 1860, from eating the berries ; two cases from eating the berries — one died, the other recovered, with impaired memory. For the purposes of this paper the writer asked of the Registrar-General a return of all cases of death from tutu poisoning that occur in the records. In his reply the Registrar-General stated that he was unable to make a return, as cases of this kind are classed in the vital statistics under the general heading " Accidental Poisoning." He had had the statistical tables relating to inquests examined for thirty years back, and found that only four deaths occurred from eating poisonous berries, one in each of the years 1889, 1891, 1896, and 1902. It is probable that the berry in each of these cases was the tutu-berry, but in only one case — that of 1889 — was it stated to be so. Effect of the Plant on Animals. Horses. — Statements vary as to the effect on horses. It is said that they have been known to eat freely of the plant without injury (8), and, again, that C. thymifolia is highly poisonous to them (9). They are said to refuse the young shoots, but have been known to eat the berries (3). If they escape, it is probably because they do not eat enough of the plant ; that they eat freely without evil result is not credible. Birds are regarded as immune. They certainly eat freely of the berries without ill effect. The cjuestion of their immunity will be considered later. Babbits are said to be immune (10), (11). and certainly the tutu does not seem to have checked their increase. They probably do not eat the plant. FiTCHETT. — Physiological Action of Tiilin. 289 Elephants. — Sir Julius von Haast (12) records the death of an elephant from tutu-poisoning. The animal was marched inland by its owner for a considerable distance, and on arriving at a suitable halting-place, where the vegetation was abundant, was allowed to feed. The grass had been burnt off during the previous season, and had shot up again, together with a large crop of tutu-shoots. The elephant fed for four hours, and then drank freely from a neighbouring stream. It then began to reel, fell on the ground, and died in three hours. Sheep and Cattle. — The following extract from a letter received from the manager of a large sheep-station gives an excellent account of the effects of tutu upon sheep : " The effect on sheep is that they will stand still, trembling as if palsied, froth at the mouth, with their jaws going continually, and their teeth grinding. Suddenly they will fall over, with their limbs rigid, as if suffering from strychnine poisoning. If assisted on to their legs they are absolutely mad, and will rush against a fence or over a precipice, and will pay no attention to man, or dog, or animals of their own kind. With animals that have eaten less of the plant, symptoms do not appear unless they are disturbed, and then the effect is shown with terrible suddenness ; a bark from a dog or a sudden run for a few yards will be almost certain to start the poison to work. In cases like the above, however, the affected sheep generally recover if left alone." In their wild career they often injure themselves against obstacles, or rush into creeks and are drowned. More frequently they die in convulsions. Cattle are similarly affected, but the wild delirium is even more marked in their case. Popularly they are said to go mad ; and the wild way in which they wheel round and round, gallop aimlessly about, kicking, charging, and rushing blindly against rocks and other obstacles, lends colour to the popular opinion. The wild career continues until the animal, overcome by exhaustion, falls to the ground, becomes comatose, and dies in con- vulsions. In the light of this account, the symptoms displayed by one of Captain Cook's animals is interesting : " The ram was taken with fits, bordering on madness. . . . One night he was seized with one of these fits and ran headlong into the sea, but soon came out again, and seemed quite easy. Presently after he was seized with another fit, and ran along the beach . . . and was never seen more " (13). Animals are frequently found distended with gas, " blown " after death. This is probably due to rapid fermentation of the leaves ingested, and is similar to the condition met with in cattle after eating freely of clover. As with clover, it is more pronounced when the tutu is eaten wet. Effect on Human Beings. The symptoms of poisoning by the plant in the human subject include vomiting, giddiness, delirium, great excitement, stupor, coma, and con- vulsions. In a fatal case reported in the Otago Colonist of the 25th October, 1861, the physician who attended the case stated in his evidence at the inquest that he found the child perfectly pale, with teeth clenched. The breathing was difficult, the lips livid, and the pupils much dilated. For about five minutes the rigidity went off. and the pupils contracted ; but a relapse occurred, the teeth were set again, and the child gradually sank back, " without any symptom of convulsion or suffering." In this case it was the 10— Trans. 290 Transactions. young shoots that had been eaten. The jury appended the following rider to their verdict : " The jury would recommend the Provincial Government to keep up a standing advertisement in the pubUc prints warning persons of the poisonous nature of the tutu plant, the young sprouts as well as the berries, and also giving descriptions of the same " (5). Lauder Lindsay (3) records several cases that had been reported to him. In one case about half a pint of berries were eaten shortly after the evening meal. No effect was produced until 6 o'clock next morning, when, on attempting to rise as usual, the subject suddenly lost consciousness till 11 a.m. He was then conscious for a minute or two, but almost immediately relapsed into stupor, which continued for about twenty-four hours. When he came to himself he had lost his memory, and for half a day was unable to say where he was, or what he had been doing for the previous forty- eight hours. He gradually recovered, and there were no subsequent bad effects. Throughout the illness he had had no pain. In another case two young men partook of some tutu-berries, about 4 p.m. One swallowed the berries, the other sucked' them but spat out the seeds. The latter was unaffected, but the former was seized with con- vulsions about 9 p.m. The convulsions continued for about forty minutes, and then the patient gradually passed into a state of coma, which continued all next day. On recovering consciousness he was utterly oblivious of the particulars of his illness, and denied having eaten the berries. He was drowsy for a few days, but gradually recovered. In a third case, retching, vomiting, and convulsions were the prominent symptoms. This case did not recover completely. A mental change, which was permanent, remained after the acute symptoms had subsided. In a fourth case, in which particulars were given by Dr. Stewart, of Tuapeka Hospital, insomnia was one of the earliest symptoms. This was followed by tonic and clonic spasms, with coma, lasting for two days. During recovery, entire loss of memory was observed. The patients — there were two — did not know where they were, why they had been brought to hospital, or what their occupation was. They did not recollect having eaten tutu. In a case noted by Dr. Hocken, the symptoms included tonic and clonic spasms lasting two days, coma, and loss of memory. Considering the highly toxic nature of the plant, it is surprising that so few deaths from poisoning are on record. In the early days probably many fatal cases occurred of which no record was made. Nowadays cases of poisoning are rare. This may possibly be accounted for by the very dis- tinctive appearance of the plant and the widespread knowledge of its poison- ous nature. No one who has once seen tutu is likely to mistake it for any- thing else, and every school-child knows that " toot " is poisonous. More- over, near the large centres of population the plant is not often now met with in places readily accessible to young children. Among flocks and herds the mortality has also fallen, not because, as is sometimes supposed, the animals have acquired immunity or tolerance, but because in the more highly cultivated districts tutu has been largely exterminated. Sheep and cattle when moved from place to place are now sent by rail rather than driven. This alone has considerably reduced the mortality, for driven animals are particularly prone to sufier, and tutu is the commonest roadside plant in many districts. The farmer, too, taught by experience, has become learned in the ways of managing his stock in relation to tutu. He takes care to avoid " toot " FiTCHETT. — Physiological Action of Tutin. 291 countr}' ill the early spring, when the too tempting and especially toxic young sprouts are appearing. If sheep are to be turned out where tutu abounds they are first fed freely on English grass, for a well-fed sheep only nibbles tutu as he happens to meet it. and escapes ; while a hungry sheep, finding it difficult to resist so ready a means of appeasing its appetite, fills its stomach, and succumbs. Indeed, it is a constant observation of farmers that tutu introduced into an empty stomach is more lethal than when taken into a stomach that already contains food. Cross-breds are said to be less readily affected than the more active and restless merino, and are therefore selected for distribution to tutu-infested areas. But, in spite of these precautions, accidents, through the ignorance of a shepherd, or the chance of an open gate, occasionally happen, and a heavy loss is experienced, as witness the following instance reported in 1905 : " A settler left sixty bullocks about four years old in a field of swedes. In his absence thev escaped from the paddock into a gully full of tutu {C rusci- folia), where, on his return, he found forty-three of them dead. Mr. Clayton found the rumen packed with tutu leaves and branchlets " (14). 2. Botany. The tutu plant belongs to the natural order Coriariece, a small order of very doubtful relationship possessing but a single genus, Coriaria. The genus includes some eight or ten species, and has a rather remarkable dis- tribution, species being met with in south Europe, South America, China, Japan, north Africa, India (Himalayas), and New Zealand. The European species, C. niyrtifolia, is well known to possess toxic pro- perties. Its leaves have been used to adulterate senna with fatal effect, and numbers of cases of death are recorded from eating the berries. In. 1862 several persons were said to be poisoned by eating snails that had been fattened on its leaves and young shoots (15). The symptoms of poisoning- include vomiting and convulsions, and, on the Avhole, closely resemble those of tutu poisoning. In 1863 Riban (15) investigated the chemistry of this species, and separated a glucoside which he named " coriamyrtin." The physiological properties of this compound will be referred to later. The Himalayan species, C. nepalensis, is stated to be non-toxic, but, as the same has been said both of tutu and of C. myrtijolia, the statement must be accepted with reserve. The fruit is said to be eaten with impunity. The American species, C. thymijoUa. and the New Zealand species are said to be identical, and this statement has been used to prove a former land-connection between the two countries. It is more Likely, however, that the order is a very ancient one, which has died out everywhere except in those places in which it is now found (8). Moreover, the identity of the two has been questioned. The species met with in New Zealand are given by Cheeseman (16) as three in number — (1) C. ruscifolia, (2) C. fhymifolia, (3) C. angustissima. The first is known locally as the " tl-ee-toot," the second as the " ground- toot," and to both the name " tutu " applies. The Maoris have no name for G. angustissima. There seems to be some division of opinion as to whether these three really constitute separate naturally distinct species, or whether the two last are merelv varieties of the first. Lauder Lindsav, who in 1868 described, though with hesitation, four species — (1) C. arhorca, (2) C. tutu, (3) C. thymi- joUa, (4) C. angustissima — says, " If only typical species be examined the 292 Transactions. student will have little difficulty in accepting the foregoing as good species well distinguished from each other by habit, but if he extend his observations to . ■ . . forms in the living state over wide areas, he will not fail to find them connected by transition states which he will frequently be puzzled to refer to one book species rather than another, partaking as they do of the characters of two or more of these species " (17) ; and he suggests that it might be preferable to regard them as mere forms of a most variable single Cheeseman says of C. thymifoha that in its ordinary state it is distinct enough, but that the large-leaved forms pass directly into C. niscifoUa, and narrow-leaved varieties into C. angusiissima (16). G. M. Thomson (18) regards C. angustissitna as a mere altitudinal variety of C. thymijolia. The botanical characters of C. ruscifolia, as given by Cheeseman, are : " A shrub or small tree with spreading 4-angled branches, very variable in height and degree of robustness, sometimes attaining 25 ft. with a trunk 10 in. diameter, at others not more than 2 4: ft., with almost herbaceous stems. Leaves 1-3 in., ovate or oblong-ovate, acute or acuminate, rounded or cordate at the base, sessile or very shortly petioled, 3 -5-nerved. Racemes drooping, many-flowered, 4-12 in. long or more, slightly pubescent. Pedicels slender, ^-^ in., bracteolate at the base. Flowers small, green, |-J in. diameter, strongly proterogynous. Sepals broadly ovate, subacute. Fila- ments elongating after fertihsation. Fruit globose, purplish-black, of 5-8 cocci, enveloped by the persistent enlarged juicy petals " (16). The herbaceous-stemmed shrub form of this is the more common. It takes this form in the open country and where the soil is dry. The roots creep and interlace below the surface, and in the spring stems shoot up from every part of the root, sometimes forming an almost impenetrable jungle. The stems may grow 10 ft. to 15 ft. in a single season. The tree form often grows solitary in the bush that lines the banks of streams. Shelter and moisture seem necessary to the attainment of this form. C. ruscifolia occurs abundantly in all three islands of New Zealand, the Kermadec Islands, and the Chatham Islands, and is met with from sea- level to a height of 3,500 ft. C thjmifolia occurs only in the North and South Islands of New Zealand ; and C. angustissima is still more restricted in its distribution, occurring only in subalpine localities in the Provinces of Otago and Canterbury. These two species differ from the former chiefly in the size of the plant and of the leaves, and in their annual habit. All three forms are met with in abundaik'e in the immediate neighbourhood of Dunedin. The tree form of C. ruscifolia may be found in the bush that lines the banks of the Water of Leith and its tributaries ; while C. thymifolia and C. angustis- sima are plentiful on the hills that encircle the town. All parts of the plant are poisonous, but the young shoots are more toxic than the leaves and fruit. The same has been noted of C. imjrti- folia (15). In the case of human beings it is usually the so-called berry that is eaten, though the shoots too are sometimes eaten by children. Of the berry, only the seed is poisonous. The strained juice is harmless, and from it the Maoris and early settlers made a non-intoxicating wine that was drunk in large quantities (19). Indeed, in the very early days the tutu was known as the wine-berry shrub. This wine, however, has not always proved to be above suspicion. Canon Stack (20) relates that on one occasion after partaking of some tutu-wine he was seized with alarming symptoms ; he lost all feeling FncHETT.— Physiological Action of Tutin. 293 in his extremities, a mist came over everything, and he thought that he was poisoned. The symptoms soon passed off, however, and he was none the worse. Cattle and sheep are especially fond of the young, tender, asparagus-like shoots, but they also eat the leaves and branchlets with readiness. 3. AVoRK OF Previous Observers. When one considers the harmful influence that this noxious plant has had upon the development of the country, it is remarkable that until recent years little effort was made to determine the nature of the poison. In 1869 Skey (21) investigated the chemistry of C. ruscifolia. He showed that the poisonous principle is not an alkaloid, as was commonly thought, and with ether extracted from the seeds a green-coloured oil, 5 minims of which when given to a cat quickly produced the symptoms characteristic of tutu poisoning. Its highly toxic nature, together with certain peculiar chemical properties possessed by it, inclined him to the opinion that this oil was the active principle. A year later, 1870, Hughes (10) attempted to separate an alkaloid, using the ground-shoots, and did indeed succeed in obtaining a crystalline sub- stance, but failed to identify it. He thought that a heavy olive-coloured oily fluid which he also obtained and proved to be toxic might be the active principle and " a liquid alkaloid similar to conia." He showed that lime destroyed the activity of the poison, and advocated its use as an antidote. In conjiinction with Dr. Acheson, he conducted a series of experiments on cats and dogs, but more with the object of proving the toxicity of his ex- tracts, and of determining the value of lime as an antidote, than with any idea of advancing our knowledge of the physiological action of the poison. Hughes's results were adversely criticized by Skey (22), who held that the temperature used in Hughes's experiments was such as must have pro- duced many side-products by destructive distillation, and among others acetate of ammonia, the presence of which, he thought, would sufficiently account for the reactions attributed by Hughes to the presence of an alkaloid. Twenty years elapsed before any further investigation was undertaken, and then, in 1890, W. L. Christie (11) examined the physiological action of the oil that had first been extracted by Skey. He made a series of ex- periments on mammals, including one upon himself, and briefly summarised the conclusions he arrived at as follows : '(1) That tutu acts on the nerve- centres after absorption into the blood ; (2) that the grey matter of the motor cortex is the part chiefly aft'ected, and that this peripheral action {sic) causes epileptiform convulsions ; (3) that vomiting is chiefly due to central causes, and that by its means, and perhaps by the renal secretion, the poison is removed from the body ; and, lastly, (-t) that dyspnoea is due to poisoning of the respiratory centres, and when death ensues it is due to asphyxia from this cause or tetanus of the respiratory muscles — both may however, I believe, occur from coma." The chief interest in Christie's work, however, lies in the experiment upon himself. He took, in all, 9 grains of an extract made from the leaves gathered in the spring. He calculates that each grain of extract represents 100 grains of leaf ; but, in the absence of data regarding the amount of tutin in tutu-leaves at different times of the year, and of details as to the exact 294 Transactions. method of making the extract, it is impossible to calculate what dose of tutin was taken in this case. The first dosB (4J grains) was taken at 2.20 on F^ida^• afternoon, and a second dose of the same amount at 4 p.m. An hour or two later he felt sick and faint, and began to vomit. The vomiting oc- curred at frequent intervals, and continued for twenty-four hours. At 8 p.m. he felt slight twitches in the legs and arms ; and at 10.40 p.m. the medical student who was acting as clerk of the case noted that " all the muscles seemed to get tight, and there was foaming at the mouth." At 10.50 the pulse-rate was 102 and the breathing heavy. Twenty minutes later the pulse was still 102, but the breathing was normal, and there was profuse perspiration. At 11.24 p.m. the clerk noted that " the subject spoke in a collected manner ; getting right, but drowsy." The vomiting continued till 8 p.m. on Saturday. The following day (Sunday) he felt sick and dull, but, though shaky, managed to attend to his duties. He states that sensation was dulled and spirits below par for seven or eight days. For a month he was not in good tone, and then for the first time he felt a sensation of " pins and needles " in his fingers and toes, and felt the floor of his bedroom woolly when he rose in the morning. He could feel accu- rately with his fingers, but experienced a heavy, stiff, numb sensation when he used them, and this symptom lasted a month. 4. The Active Principle. The first substantial advance in the investigation of the chemical pro- perties of tutu was made in 1900, when Easterfield and Aston (23) suc- ceeded in isolating a crystalline glucoside, to which they gave the name " tutin." All three species of Coriaria Avere experimented upon, and crystals of tutin were obtained from each. The young shoots were found to yield a greater quantity (0-03 per cent.) than either the berries or the leaves. Preparation : In the case of C. ruscifolia, " the fresh young shoots were finely divided, the juice expressed, filtered, and evaporated to a syrup nearly neutralised by carbonate of soda and shaken up with ether. The ether on evaj)oration deposited crystals of tutin. These were recrystallized from alcohol until the melting-point was constant." Properties : Tutin is described as a colourless, odourless, intensely bitter compound, which separates from alcohol in oblique-ended prisms, and from hot concentrated solutions in water in characteristic acicular forms. It is perceptibly volatile, sublimes readily at 120° to 130° C, and melts at 208° to 209° C. (uncorrected). It contains no nitrogen, and reduces Fehling solution after inversion by acid. The compound is therefore to be con- sidered a glucoside, but the hydrolyzed substance yields with phenylhydra- zine an amorphous precipitate which is not phenylglucosazone. Examination by Zeissl's method for methoxyl groups gave negative results. Strong sulphuric acid added to a few drops of a saturated aqueous solution of tutin gives a blood-red coloration. Solubility : 100 grams water at 10° C. dissolve 1-9 grams tutin ; 100 grams ether at 10° C. dissolve 1-5 grams tutin ; 100 grams alcohol at 10° C. dissolve 8-2 grams tutin. It is very soluble in acetone, sparingly soluble in chloroform, and soluble in benzine and carbon-disulphide. The optical activity has been determined by Marshall. The substance is dextrorotatory, and the specific rotatory power is -f- 9-25°. Easterfield and Aston found that when solutions of tutin were evaporated to dryness- FiTCHETT. — FJiysioloijical Action of Tutin. 295 with slaked lime the tutin underwent decomposition, and could not be recovered. This fact recalls Hughes's statement that lime destroyed the activity of the tutu poison. The close relationship of the New Zealand tutu to the European ('. myrtifolia, together with the fact that Lauder Lindsay (17) and others have thought it probable that the active principle of tutu is coriamyrtin, lends interest to the following table of differences existing between the two bodies, as given by Easterfield and Aston (2.3) : — Coriamyi'tin. Tutin. Melting-point . . . . 220° C. (according to 208° C. Merck. 229° C.) Carbon . . . . . . 64-1 per cent. 60-7 per cent. Hydrogen . . . . . . 6-6 per cent. 5-8 per cent. With hydriodic acid and potash (lives fuchsia-red Gives nil. colour Solubility in 100 parts of water 144 at 22° C. 1-9 at 10° C. Effect on pupil . . . . Contracts it Dilates it. It may be said here, and will be shown later, that tutin has little, if any, action on the pupil when applied locally. The physiological activity of the new compound was put to the test by Mr. Gilruth (23), then Chief Govermnent Veterinarian in New Zealand. He administered to a pig weighing 17 kilograms, 0-129 grams of tutin, dis- solved in water and mixed with half a pound of pollard. In half an hour uneasiness and spasmodic movements of the jaws were observed ; then the breathing was noticed to be accelerated, and vomiting occurred. The symptoms gradually increased in severity, until the animal was seized with tetanic convulsions. The convulsions were at first separated by intervals of about fifteen minutes, but they gradually increased in severity and fre- quency until they became almost continuous. Each convulsive seizure, after beginning with a tonic spasm that lasted half a minute, was accom- panied by screaming and stertorous l)reathing. Finally the animal died in a convulsion five hours after the poison had been administered. Further experiments on cats testified to the marked toxicity of the com- pound— e.g., a dose of 0-01 gram killed a kitten weighing 1 kilogram in forty minutes ; 0-001 gram administered to a cat weighing 2 kilograms caused a fit in three hours and illness for the next twenty-four hours. The same cat was afterwards killed by a dose of 0-003 gram. A dose of about a milli- gram caused nausea, vomiting, and incapacity for work for twenty-four hours in a full-grown, healthy man. B. ORIGINAL WURK. (For full details of the experiments, see Protocols;) 1. General Action of Tutin on Mammals. [a.) Action on Cats. The effect of various doses upon cats will be shown first. Effects of a large dose : 9-8 mlgm. tutin (3 mlgm. per kilo body- weight) were injected under the skin of a full-grown female cat, weighing 3-28 kilo- grams (Exp. 1). The animal was placed in a hutch, and watched continuously- Four minutes after the injection it was noticed that respiration was very rapid (48 to the quarter-minute). The animal seemed sleepy and dazed, 296 Transactions. and curled itself down as if to sleep, but at once raised its head, opened its mouth, and panted for breath, like a dog on a hot day. It moved its head slowly from side to side in a dazed, stupid way. Seven minutes after the injection, thick, ropy saliva began to pour from the open mouth, the respirations were even more rapid, and were now audible, almost stertorous, and the whole body was shaken with the force of the respiratory effort. The pupils at this stage were moderate. Ten minutes after the injection the animal got up and began to walk cautiously about the hutch, picking its way like a cat crossing a muddy street. Half a minute later it was sud- denly seized with a violent convulsion, which in every respect resembled a typical epileptic fit. The animal fell on its side, and all the muscles of the body were thrown into intense tonic spasm. The head was bent firmly backwards, the back hollowed, the fore and hind limbs rigidly extended, the digits widely separated, the claws extruded. The hairs of the tail became erect, urine and fax-es were shot out with considerable violence, the pupils were widely dilated, respiration entirely ceased, and the nose became cyanosed. This tonic spasm lasted thirty seconds, and was followed by clonic spasms affecting the neck, jaw, limbs, and respiratory muscles, which lasted twenty-five seconds more. As the fit passed off, the pupils contracted, the respirations became deeper and slower, and the nose recovered its normal appearance. An interval of five seconds was followed by another fit like the first, but the tonic stage did not last so long, and the clonic spasms were more marked. Fit succeeded fit in rapid succession. There were no voluntary cries, but the violence of each seizure caused a choking noise as the air was driven through the glottis. Between the fits the pupils always contracted, and they began to dilate just before each convulsion occurred ; during the fit they were dilated to the widest possible extent. This alterna- tion happened so invariably that a commencing dilatation of the pupil could be taken as an indication that a convulsion was imminent. As the animal became exhausted the fits diminished in severity and frequency, the re- spirations became irregular, infrequent, and gasping, and finally death occurred thirty-one minutes after the injection. From the first the animal gave no indication that it suffered any pain, and from the onset of the con- vulsions it was unconscious, without either ear or conjunctival reflex. The temperature at death taken in the rectum was 102-4° Fahr. On fosi mortem examination the right horn of the uterus was found to contain a nearly full-sized foetus, which looked as if it had also been aft'ected with convulsions ; one hind leg was twisted over the other, the right forepaw was behind the right ear, and the claws were extruded. Beyond some small haemorrhages in the lungs and a marked congestion of the brain and cord there was nothing noteworthy. In the next experiment (Exp. 2) the dose was reduced to 2 mlgm. per kilo body-weight, 7 mlgm. of tutin being injected under the skin of a cat weighing 3-5 kilograms. The first symptom noticed (ten minutes after the injection) was trembling of the head and fore part of the body. This was followed, fourteen minutes after the injection, by rapid breathing (56 to the quarter-minute) and by salivation. At twenty-one minutes, slight twitching of the eyelids and ears was noticed. At twenty-four minutes the animal defax-ated, discharging a large quantity of ffeces. At twenty- five minutes the twitching, which had been gradually getting more marked and more extensive, was severe. At each attack the pupils dilated, but returned to the normal size when the twitching ceased. The respirations were irregular, exaggerated, and suggestive of the Cheyne-Stokes type. FiTCHETT.—Phjjsiolocjical Action of Tutin. 297 At twenty-nine minntes the animal was seized with a general convulsion, the tonic stage lasting thirty seconds. From this point the convulsive movements continued almost without intermission until the end. The clonic spasms were the more in evidence, but every now and then a tonic seizure would arrest the movements for a few seconds. Gradually the movements became more and more feeble, the respiration slow, irregular, and gasping, and finally the animal died in a tonic spasm fifty- one minutes after the injection had been given. In this case the symptoms appeared more gradually, and the cerebrum seemed less affected than in the first cat. The animal was less dazed and stupid, and frequently " miaued " in a plaintive way, especially after the twitching began. The twitching was a marked feature ; it began in a small way, affecting only the eyelids and ears, but the attacks increased in frequency and in severity, and gradually more and more muscles became involved. In the earlier stages, when only the face and neck muscles were afEected, the cat at each attack presented the appearance it might have done had it been held and a rapid series of electric sparks discharged close to its face. Later, when the muscles of the shoulders and fore legs were involved, the twitching caused little springs into the air and down again with the fore part of the body, suggesting the appearance of a puppy pouncing at play. When the twitching had got the length of involving the shoulders, it very soon took the form of a general convulsion, and in this case, once convulsions had set in, the svmp- toms which followed were much the same as seen in the first cat. In the next experiment (Exp. 3) the dose was considerably reduced, 1-7 mlgm. being injected under the skin of a cat weighing 2-394 kilograms. This is equivalent to 0-75 mlgm. per kilo body-w^eight. Nothing was noticed for half an hour, and in that time the cat looked quite normal. It then began to swallow rather frequently, as if swallowing saliva, and then suddenly got up and defsecated. It then began to breathe rapidly, saliva could be seen dripping from the mouth, and it vomited. It again attempted to empty the bowels, and now looked miserable, and kept up a constant complaint, though if spoken to it would come forward and purr. Twitching of the face did not appear till thirty-five minutes after the injection, and the first convulsion occurred at forty-one minutes. It lay on its side for a few minutes after the convulsion, and then got up and walked about the cage. Its condition now was much improved on what it was before the convulsion occurred. The breathing was easy, salivation seemed to have ceased, and the twitching which had so annoyed and alarmed the animal was not noticed ; but the improvement was not for long. In about a quarter of an hour it began to breathe quickly again, and the twitching returned, and gradually got more and more severe till it culminated in a general con- vulsion at seventy minutes after the injection. This was a most severe tonic spasm, which lasted four minutes and a half by the watch, and during that time the animal w^as not seen or heard to draw a breath. From this onwards convulsions continued with intervals of only a few seconds till death occurred, one hour and forty-nine minutes after the injection. In this cat the cerebrum seemed less affected than was the case with the other two. It continued alive to its surroundings almost to the end, and " miaued " voluntarily five minutes before death. It never rose after the second seizure, though it once or twice attempted to do so, and was thrown down by a convulsion. In the intervals between the attacks, running or swimming movements were noticed. In the next animal experimented upon (Exp. 4) the dose was reduced 298 Transactions. to 0-375 mlgm. per kilo of body-weight, 1 mlgm. of tutin being injected under the skin of a cat weighing 2-688 kilograms, and, curiously, symptoms made their appearance earlier in this case than in the last. It defsecated and began to breathe quickly within twelve minutes of the injection ; saliva- tion was noticed at fourteen minutes, and at twenty-four minutes it was panting with its mouth open, and vomited. Twitching appeared at thirtv- two minutes, and the first convulsion occurred at fifty-five minutes. Con- vulsions were severe and frequently repeated, and it was thought that the cat would die. It had a severe convulsion at 6.5 p.m., and it was not seen again till 7-15 jj.m. It then appeared rather tremulous, and was easily startled, bu.t presented no further symptoms, and was quite well next day. It would seem that 0-375 mlgm. per kilo is very near the minimum lethal dose. In the last three cats the constant symptoms were defsecation, rapid breathing, salivation, twitching, and general convulsions, and these generally made their appearance in the order named. The first cat did not defaecate voluntarily, and neither of the first two vomited. The vomiting in the last two occurred only once in each case. In the first convulsion in each case the tonic stage was the more pronounced, and was invariably of the opisthotonic type. Later, clonic spasms were more in evidence, and with lethal doses, when the case was making towards a termination, movement was hardly absent for a moment. With the larger doses the effect upon the mental activities of the animals vras very marked. From the first they seemed dazed, and once general convulsions had set in they were oblivious of everv- thing. With the smaller doses the cerebrum was little affected, and often after the most severe and prolonged convulsions, in the case of the cat that recovered, the animal would rise and behave as if little had happened, answer- ing when spoken to, and even purring. (6.) Action on Babbits. Kabbits are less readily affected by the poison. The largest hypodermic dose recovered from was 2 mlgm. per kilo (Exp. 5), (in a cat, 0*75 mlgm. per kilo proved fatal). A dose of 2*5 mlgm. per kilo was fatal in two hours and a half (Exp. 6), and doses larger than this killed rather rapidly (Exps. 7, 139). By oral administration a much larger dose than this is required to kill — e.g., in Exp. 8, 7'5 mlgm. per kilo proved fatal in two hours ; in Exp. 9, 6 mlgm. per kilo was fatal in twelve hours ; while in Exp. 10, 5 mlgm. per kilo was recovered from. In one case (Exp. 161) death preceded by typical symptoms followed the instillation of four drops of a 0"5-per-cent. solution into the conjunctival sac. Attempts to poison rabbits with fresh tutu-leaves failed, for the animals, though deprived of all other food for several days, steadfastly refused to eat. Symptoms. — No important symptoms appear that have not been men- tioned as occurring in cats. After a lethal dose the animal at first appears dazed, tends to assume unnatural attitudes — e.g., lies on the abdomen, with the legs projecting in front and behind — and the gait is altered. Eespiration soon becomes very rapid, and there may be salivation, though it is not so marked a symptom as it is in cats. Alteration in the size of the pupil is not so noticeable. Twitching of the eyelids, lips, ears, and fore- paws occurs, and is followed by general convulsions. In the convulsion the tonic spasms are not so evident as they are in cats, but they do occur, and are of the opisthotonic type. As a rule, after the first violent con- vulsive movements are over, the animal continues lying on its side, and FiTCHETT. — Physiological Action of Tutin. 299 shows almost constant movement, either clonic spasms or running-move- ments, chiefly of the fore paws, until exhausted. Urination occurs during the convulsions, but, of course, vomiting was not observed. The animal utters no cry, and indicates in no way that it suffers pain. In the later stages it is comatose, and usually dies from exhaustion. (c.) Action on Guinea-pigs. No series of experiments was made to determine the minimum lethal dose in these animals, but it would appear to be rather smaller than in rabbits. A dose of 2 mlgm. per kilo caused symptoms in thirty minutes and death in seventy minutes in one case (Exp. 11), while a dose of 1 mlgm. per kilo caused convulsions, but the animal recovered (Exp. 167). A young guinea-pig was killed by a dose of 1 mlgm. per kilo, while another •of the same age (five days) showed symptoms with 0'75 mlgm. per kilo, but recovered. It would appear from this that the young guinea-pig is more easily affected than the adult. By oral administration a dose of 1*5 mlgm. per kilo was insufficient to produce obvious symptoms, but a dose of 2 mlgm. per kilo repeated in forty-eight hours caused death (Exp. 13). The symptoms are very like those shown by rabbits — viz., unnatural attitudes, rapid breathing, twitching, general convulsions, and running movements of the limbs. The spasms are more clonic than tonic. When convulsions first appear, the animal tumbles and tosses about in every direc- tion, but soon takes up a position on its side, and then continues in constant inovement until exhausted (Exps. 14, 167). 2. Action on Birds. It is the common opinion that birds are immune to the tutu-poison. It were not strange did a relative immunity exist, for the plump, sweet, attractive-looking berries seem to have been designed by nature for the especial purpose of inducing birds to eat ; and that they do eat them freely and without injurious effect is certain. Mr. Maning, author of " Old New Zealand," quoted by Lauder Lindsay (3), says, " Many kinds of birds live entirely on the tutu-berries when in season. . . . The tui {Prosthemadera novce-zealandice) I have kept tame and fed for months on nothing else." Again, birds differ from mammals in having a higher rate of oxidation, a higher temperature, and a peculiar metabolism, which results in the excretion of urates instead of urea in the urine — features which might conceivably have an important bearing on the question of their possible immunity. Christie (11), as the result of experiment, inclined to the general opinion that birds are immune. He injected in all 40 minims of an ethereal solution of " oil of tutu " into the " chest cavity " of a young rooster. Beyond some slight symptoms which were attributed to the ether, and a marked increase in the frequency of defsecation, no characteristic effect was noted. He observes that " there was no twitching, although the dose (40 m.) is twice as much as is necessary to convulse a cat " ; and concluded that the bowels are chiefly affected in birds, and that, therefore, they are saved by rapid excretion by this channel. When the above statement is more closely examined it is found that Christie administered probably not more than 1 mlgm. of pure tutin per kilo. The symptoms were wanting because the dose was inadequate. 300 ■ Transactions. Experiments that have been made by the present writer on pigeons prove that birds are not immune to tutin. The minimum lethal dose by mouth, however, was found to be high, and this probably accounts for the apparent immunity, the ingestion of very large quantities of berries being necessary to produce toxic symptoms. In the first experiment (Exp. 15) it unfortunately happened that the pigeon used displayed a peculiar tolerance to the poison. This misled to the belief that the minimum lethal dose was much higher than it really is. The bird, weighing 314 grams, was subjected to successive doses, equivalent to 2, 4, 6, 8, 10, 12, 16, 20 mlgm. per kilo of body-weight. The solution of tutin was given by the mouth, and the experiment extended over a period of ten days. The smaller doses had little effect. For a few hours after each dose the bird was dull, apathetic, and disinclined to eat or move about. It stood in a corner of the cage, with its feathers pufiecl out, blinking heavily, and presented the appearance of a bird that had overeaten itself, and was trying hard to go to sleep, but was too uncomfortable to succeed completely. The last dose (20 mlgm. per kilo) was given on an empty crop, and as no ill effect was anticipated — it being thought at this time that in all probability birds really were immune — it was not closely watched. But forty-five minutes later attention was attracted by the flapping of its wings, and it was found lying on its back in convulsions. One hour after the administration of the poison it was dead. Its weight at death was 345 grams — a gain of 31 grams in ten days, which would seem to indicate that tutin has no injurious influence on general metabolism. That the bird actually received the doses stated is quite certain. The sokition was very carefully measured in a hypodermic syringe having a running-nut on the piston-rod, and dropped into the beak, which was held open by the finger. There was no difficulty in the administration, and every particle of the fluid was swallowed. As 20 mlgm. per kilo was obviously too great a dose, it was decided to give to the next bird 1 mlgm. per kilo in excess of the largest ineffective dose on the first bird. To this end a dose equivalent to 17 mlgm. per kilo was administered by mouth to a fasting pigeon weighing 319 grams (Exp. 16). In this case toxic symptoms — viz., twitching and tremulousness of the head and wings, and attempts to vomit — made their appearance within two minutes, violent convulsions appeared in four minutes, and death occurred sixteen minutes after the administration. In contrasting these two experiments, it will be noticed that the " time to kill " was greater in the first case by forty-four minutes, although the dose exceeded the dose in the second case by 3 ml^m. per kilo. This observation, taken in conjunction with the fact that symptoms did not appear in the first case with a dose of 16 mlgm. per kilo, suggested the possibility of the first pigeon having acquired some degree of immunity or tolerance by the poison having been administered in gradually increasing doses over a lengthened period. To test the validity of this supposition, another pigeon was treated in the same way (Exp. 17). The experiment extended over a period of three weeks, and a maximum of 10 mlgm. per kilo was reached without the appearance of any marked symptoms, but 12 mlgm. per kilo proved fatal. The rapidity with which syihptoms ensued after a dose of 17 mlgm. per kilo, and the speed with which a fatal termination was reached, pointed to the dose being well above the lethal minimum. A dose equivalent to 15 mlgm. per kilo was therefore given by mouth to a pigeon weighing FiTCHETT. — Physioloyical Action of Tutin. 301 357 grams (Exp. 18). No symptoms followed beyond those that generally appeared in the first experiment after a non-lethal dose had been adminis- tered. One hour and three-quarters later the bird was apparently normal, and on the day following the experiment was quite well. Here a dose of 15 mlgm. per kilo was without efTect. It was noted that the crop in this bird was full, but, though this was recognised as probably influencing the result in some degree, the fact that the first bird was unaffected by a dose of 16 mlgm. per kilo was so striking that it was thought likely that 15 mlgm. per kilo was below the lethal minimum. It was therefore decided to give a dose equivalent to 16 mlgm. per kilo to another pigeon (Exp. 19). In administering the poison to this bird, by an accident a few drops of the solution were lost, and the deficiency was made good by an allowance of 5 extra minims (Exp. 15). In three minutes the bird was in convulsions, and in nine minutes was dead. As no satisfactory conclusion could be drawn from this experiment it was repeated (Exp. 20), but the subject became convulsed within a minute and a half, and died five minutes after the administration. It was then decided to repeat the dose of 15 mlgm. per kilo, using the bird that had previously withstood this dose, but taking care that its crop should be empty (Exp. 21). At 5.14 the dose was given. No symptoms appeared till seven minutes had elapsed, when it began to retch. In twenty minutes convulsions appeared, and in thirty-five minutes it was dead. It was noted that the onset of symptoms was slower and the time to kill longer in this case than in the case where 16 mlgm. per kilo were given (thirty-five minutes as against five minutes). It was therefore thought worth while to repeat the dose of 15 mlgm. per kilo, using a bird that had not been starved. This was done (Exp. 22), with the result that the bird died in twelve minutes. It being now clear that the minimum lethal dose was much exceeded, two pigeons were taken (Exps. 5, 23, 24), and to one was given a dose equiva- lent to 13 mlgm. per kilo, to the other 12 mlgm. per kilo. In the case of the bird with the larger dose, death resulted in nineteen minutes ; but the bird that had received 12 mlgm. per kilo showed a very gradual onset of symptoms, and did not die till two hours and sixteen minutes after the administration. This bird was a young one (still squeaking), though it weighed 363 grams. It was thought that the age in this case may have influenced the result, so a dose of 12 mlgm. per kilo was given to an adult bird. Death occurred, however, in forty-six minutes — a hundred minutes earlier than in the case of the young bird (Exp. 25). A drop in dosage was now made to 9 mlgm. per kilo, and the bird that received this dose was not affected (Exp. 26). The same result was noted in a bird receiving 9'5 mlgm. per kilo (Exp. 27) ; but the next bird, which received a dose of 10 mlgm. per kilo, died in forty-five minutes (Exp. 28). This was a young bird (squeaking), weighing 330 grams. The same dose (10 mlgm. per kilo) was therefore given to an adult bird (Exp. 29), which recovered after exhibiting symptoms such as vomiting and slight convulsive movements of the wings. Of the four birds that had received 10 mlgm. per kilo, one only (a young bird) had died. A dose of 10*25 mlgm. per kilo was therefore given to an adult bird, with the result that it died in seventy-five minutes (Exp. 30). The results of these experiments are tabulated on the following page (Table 1). 302 Transactions. Table I. Pigeons. — Minimum Lethal Dose. Exp. Ko. Weight. Mlgm. per Kilo. Crop. Age. 1 Result. Time to kill. Grams. Minutes, 15 1 314 2,4,6,8,10, 12, 16, 20 Half-full .. Adult Died 60 16 2 319 17 Emptv // • • // • • 16 19 8 374 16 Half-full .. // • • n • • 9 20 4 319 16 Full N • • w • ■ 5 18 5 357 15 // • • „ • • Recovered , , 21 6 345 15 Empty // • • Died (same bird as No. 5) 35i 22 7 203 15 Half.full .. // • • Died 12 23 8 375 13 Full Young // • • 19 24 9 863 12 w • • w • • 136 25 10 386 12 // • • Adult « 46 17 11 870 1-5,2,4,7, 9, 9-5, 10, 12 Half-full .. // • • // • • (?) 30 12 315 10-25 ,^ , ^ ,/ 75 28 13 830 10 Full Young // • • 45 29 14 368 10 ff • • Adult Recovered 27 15 365 9-5 „ f> • • „ 26 16 305 9 Empty " ti • • •• It will be seen that the highest dose recovered from was 10 mlgm. per kilo, and the lowest dose that killed was 10-25 mlgm. per kilo. It may be taken as proved, then, that birds are not really immune, as has been sup- posed, but they are able to withstand a very high dose of the poison by oral administration. In noting the current opinion that birds are immune, Easterfield and Aston state (7) that cases have come under their notice in which domestic fowls have been poisoned by eating tutu-berries. This seems barely credible. The lethal dose by the mouth in birds is so high, the percentage of tutin in the seeds so low, the size of the berry in proportion to the size and number of the seeds it contains so great, that it may be doubted if the crop of the ordinary fowl could comfortably accommodate the large number of berries that would be required to provide a lethal dose of tutin. For example, Easterfield and Aston found (7) that the dried seeds of C. ruscifolia contained 22-8 per cent, of a green oil, of which 0-18 gram administered to a small kitten produced only very mild symptoms of poisoning. Assuming that this 0-18 gram contained 0-0003 gram tutin — a dose which the present writer has found to be feebly toxic to a cat (Exp. -i) — the amount of tutin in the dried seed must be about 0-038 gram in 100 grams. The minimum lethal dose by the mouth in birds is just over 10 mlgm. per kilo, so that in order to get a fatal result, a bird weighing 0-3 kilo (the average weight of a pigeon) would require to eat a little more than 8 grams dried seed, or 150 grams — over 5 oz. — of the fresh fruit. (This statement is based on the relative weights of seeds and berries.) An average-sized domestic fowl would require about 1 lb. of the fruit, and that, of course, assuming that all the tutin would be extracted from all the seeds. To throw light on this point, 5 grams (all that was at hand) of cleaned dried seeds bound with a Uttle moist flour were fed into the crop of a pigeon weighing 314 grams (Exp. 31). It displayed FiTCHETT. — Physiological Action of Tutin. 303 no symptoms, was quite well the next day, and continued well. Apparently unchanged seeds were recovered from the faeces. An attempt was made to induce a domestic fowl to eat some of the fresh fruit (Exp. 32). After being deprived of food for two full days, it was offered a heaped plateful (5 oz.) of berries. After eating about 1 oz, to 1^ oz. it desisted, and ate no more, although it had no other food given it for two days longer. It displayed no symptoms. The immunity of birds from poisoning by the seeds under natural con- ditions may be explained perhaps by — (1) The large number of seeds that must be ingested in order .to provide a lethal dose ; (2) the seeds being small and hard, and probably passing through the animal unchanged, as was noted to be the case in Exp. 31. Their relative immunity may possibly be ac- counted for in some measure by — (1) The higher rate of oxidation ; (2) the fact that the kidneys in birds are able to secrete substances in a semi-solid condition, certain normal constituents of the urine — urates and uric acid — having been observed by Bowman (25) in the cells of the tubules. This would suggest that the excretory power of the tubule cell for insoluble substances is greater in birds than in mammals. If this suggestion be applied to the case of a poison that is with difficulty soluble in water circulating in the blood, it may be conceived that this special power of the tubule cell in birds will allow of a more rapid elimination of the toxic body, and so confer a relative immunity. This, of course, applies where the poison is gradually received into the blood, as when absorbed from the alimentary tract. Where, on the other hand, the toxic body is rapidly introduced into the blood, as when given hypodermically, the cells of the tubules have not an opportunity of exercising their special power, and so the relative immunity is not so marked, or does not obtain. This may be illustrated by Exp. 53, where a dose of 5 mlgm. per kilo was given hypodermically to a pigeon weighing 335 grams, with the result that convulsions appeared in twenty minutes, and continued without intermission till death occuiTed, forty-two minutes after the injection. The question of the relation of the Hver to a glucoside like tutin is an interesting one, and especially so in this connection. In birds the veins from the crop are branches of the jugulars, and therefore a toxic body absorbed from the crop, as must have been the case in the experiments cited, enters the circulation direct. In mammals, on the other hand, the gastric vein discharges the blood from the stomach — which, so far as the absorption of poisons is concerned, corresponds to the avian crop — into the portal vein, and therefore the toxic body must pass through the liver before it enters the general circulation. Has the liver-substance any power to increase or decrease the toxicity of tutin ? To determine this, experiments were made on fish. The result was doubtful, but the indications are that the liver- substance does increase the toxic power, possibly by separating the glucose part of the compound from the poisonous part, and so freeing the latter of an innocuous encumbrance. Symptoms in Birds. — With a massive dose the animal is almost immedi- ately, with hardly any premonitory symptoms, seized with general convul- sions. The wings are rigidly extended to the full, and are flapped violently. The head is retracted till it lies firmly pressed against the back between the wings, and the bird is thrown over backwards. It turns over and over, and flops about in every direction until exhausted. This period of violent movement does not last more than a few minutes. A final somersault lands the bird on its back, and it lies, with its head drawn back beneath its body, 304 Transactions. in continuous movement — flapping its wings and clawing at space with its feet. Respiration is spasmodic, and the forcible expulsion of air from the lungs is distinctly audible. The pupils are widely dilated — no iris being visible — and the bird is in a state of coma, obUvious to everything, and apparently suffering no pain. In the later stages the head is brought for- ward, the eyes are kept closed, and the movements, which have continued without intermission from the onset, gradually become more and more feeble, and finally cease at death almost imperceptibly. The legs continue in movement longer than the wings. With a smaller though still lethal dose the first change is a heaviness and drowsiness, giving the bird a peculiar sleepy, stupid look. The eyes are blinked heavily, and seem to be kept open only with the greatest difficulty. This is succeeded by attempts to vomit, and, if the crop contains anything, by actual vomiting. Then follow tremulousness of the head and wings and sharp spasmodic blinking of the eyes. The head is frecjuently drawn back sharply, and one or other or both wings are involuntarily ex- tended for a moment. These seizures of the head and wings recur at frequent intervals, and gradually become more severe, making it difficult for the bird to keep its feet. In the more severe seizures it is thrown back on to its tail, and sits there for a moment until the clonic movements of the extended wings have ceased. At last the bird is thrown over on to its back, and, with continuous convulsive movement, the case hastens to a termination. With non-lethal doses little is to be observed beyond the initial drowsi- ness and tremulousness, and perhaps vomiting and slight convulsive move- ments of the wings. In none of the experiments did any of the birds recover that reached the stage of being thrown over on to the back. In none of the birds experimented upon was Christie's observatioii repeated that there is increased frequency of defsecation. 3. Action on Reptiles. The only animals of this class available for experiment were three small lizards of the species Lygosoma moco, the common lizard of New Zealand. They are very small animals, these specimens weighing 4, 5, and 7 grams, and are not very suitable for experiment. (Exp. 33.) The first lizard (4 grams) was given a dose 5 mlgm. per kilo by hypodermic injection, and it became convulsed, and died in about two hours. The second lizard (7 grams) (Exp. 34) received 4 mlgm. per kilo hypo- dermically, and died four hours and three-quarters later, after showing severe and oft-repeated convulsions. Opisthotonos was well marked, the animal bending backwards till head and tail met. There were also very definite clonic spasms of the limbs. For over an hour the animal was in almost constant movement, contorting itself and twisting in every direction. (Exp. 35.) To the third lizard was given a dose of 3 mlgm. per kilo, but beyond exaggerated respiratory movements it displayed no symptoms, and was quite normal on the day following the injection. Lizards are therefore affected in the same way as other animals. The lethal dose is between 3 and 4 mlgm. per kilogram. 4. Action on Aimphibia. The frogs experimented upon belong to the species Hyla aurea. This is not the native frog of New Zealand, but has been introduced from Aus- FiTCHETT. — Physiological Action of Tut in. 305 tralia, and is now the common frog. They were kept till wanted in a large wooden box, in a cool, dark cellar, and supplied with water and fresh grass- sods, but no special provision was made for feeding them. Under these conditions they lived well, and remained healthy. Sijmptoms (Exps. 54 to 58 inclusive). — With a lethal dose, the first symp- tom usually noticed was increased frequency of the respiratory movements. To this succeeded lethargy and muscular enfeeblement, the animal crawling in a laboured way, and trailing its hind limbs. If touched now it would attempt to hop, but made little progress from inability to draw the hind limbs completely beneath the body. If left alone it would lie prone on the belly with the limbs extended, and make no effort to move. When con- vulsions occur, as they usually do, though they are not such a marked feature as in mammals, tonic spasms are as a rule more apparent than clonic, and the hind limbs more affected than the fore limbs. Often the animal raises itself rigidly to the full extent of the fore limbs, and opens its mouth spas- modically two or three times in succession. If handled much, or compelled to undergo severe muscular exertion, such as struggling violently to recover the normal position when placed on the back, convulsions appear at once. This recalls the fact that a " tooted " sheep often displays no very obvious symptoms until it is " worked." A series of experiments was made to determine the minimum lethal dose (Exps. 36 to 52 inclusive), and the results are presented in tabular form below (Table II). In the early experiments the animals, after receiving the injection, were placed under bell-jars on the laboratory-table. Here they were deprived of moisture, and exposed to a strong light. Under these experimental conditions the results were confusing, frogs with larger doses displaying no symptoms, while animals with lesser doses died. The method was therefore improved upon. Each frog after receiving its in- jection was placed in a small box containing a moist grass-sod in a cool, dark cellar, and a striking uniformity in result was at once obtained. Table II. Frogs. — Minimum Lethal Dose. Exp. No. Weight. Dose. Eesult. Remarks. 36 27-5 grams 1 mlgm. par kilo Died Unfavourable surroucdings. 39 17-3 „ 1 Recovered „ 37 28-4 ,. 2 Died ^, 40 25-1 „ 2 tf • • „ 38 33-7 „ 3 Recovered ,^ 41 32 3 « // 42 31 4 „ Under improved conditions. 43 41 5 „ „ 44 40 7 ,, ,, 45 18 9 ^^ „ 47 36 9 // ^^ 49 23 9 ,^ „ 46 38 10 Died „ 48 31 10 Recovered „ 50 39 10 // ,^ 52 40 10-25 „ Died „ 51 30 11 " " Table 11 shows that the highest non-lethal dose attained w^as 10 mlgm. per kilo. Doses of 10-25 mlgm. and over were invariably fatal. Of the frogs 306 Transactions. that received 10 mlgm. per kilo, one died, and both the others showed con- vulsions and were very ill for more than twenty-four hours. Severe symp- toms were also present with 9 mlgm. per kilo. It was noticed that frogs experimented upon in the winter were more susceptible to the poison than those used in the summer. The relatively high lethal dose of tutin in frogs may have some connection wdth their mode of respiration. To a large extent this is cutaneous, and therefore a drug such as tutin, which owes its lethal power largely to its in- fluence on the respiratory centre, might a priori be expected to be less lethal to these animals than to those that have only a lung-respiration. The fact that lizards, which have a dry skin and presumably only a slight cutaneous respiration, succumb to about one-third the lethal dose for frogs points in this direction. Even with large doses the course of events in frogs is comparatively slow. For example, in Exp. 54, where about 60 mlgm. per kilo was given, the animal lived for an hour and a half. 5. Action on Fishes. (a.) General Action. There is an advantage in using small fishes to test the pharmacological action of drugs, because large numbers can be dealt with, and thus the factor of idiosyncrasy, which so often confuses results, is in great measure eliminated. Moreover, fishes can be placed in a watery solution of the drug, and the symptoms and time taken to kill easily noted. Eecently SoUmann (26) has used funduli and sticklebacks in this way, and suggests that the method might be used to study the antagonism of diaigs. In the first experiments of this kind undertaken by the present writer young trout prociu'ed from a fish-hatchery were used. The fry were kept till required in a trough with an overflow, placed beneath a running tap, and were fed on fresh minced liver. The experiments were carried out in the following way : 60 or 100 c.c. of tap-water, to which a solution of tutin had been added in definite quantity, were placed in a small wide beaker, and the fish transferred to it. Several beakers containing various strengths of tutin, and one beaker containing tap-water only, as a control, were set on together, and watched at intervals during the day. Symftoms. — The young trout were about 1 in. to 1^ in. long, and in good condition. When first placed in the test-beakers they became very excited if the tutin solution were strong. After a period of excitement, during which rotatory movements on the long axis of the body were fre- quently seen, they became quieter, and then it was noted that the gill- movements were much exaggerated. After a time they lost their power of maintaining equilibrium, and lay on one side gasping. From this position they would frequently spring up and swim round the vessel, still on the side, and then resume their position on the bottom. Shortly before death they often turned belly upwards. Minimum Lethal Dose. — In order to determine the minimum lethal dose, solutions of different strength were tried, and the results are given in the next table (Table III). In these experiments the quantity of fluid used was small. Death frequently occurred in the control when the experiment lasted over twelve hours. But the results show that the fatal effects begin when the per- centage is about 0-001, and are very definite at 0-004 per cent. This cor- FiTCHETT. — Physiological Action of Tutin. 307 responds to a dose of 10 to 40 mlgm. per kilo. For example, if we consider that a dose of tiitin — say, 10 mlgm. per kilo — injected under the skin of a mammal becomes rapidly and equally diffused through all parts of the body, its concentration at any point would be 001 gram (10 mlgm.) per thousand. In the case of a fish floating in a solution of tutin, the amount of the fluid is so much larger than the fish that the diffusion of the tutin into its body will not materially reduce the concentration of the poison in the fluid, and so the tissues of the fish will be subjected to the action of 0-001 per cent., or 10 mlgm. per kilo. The fatal dose in fish may there- fore be said to be about 40 mlgm. per kilo under these experimental condi- tions. Table III. Fishes (Trout-fry). — Minimum Lethal Dose. Exp. No. Percentage of Tutin in Water. Volume. Number of Fish. Time necessary to kill. 59 C.c. 10 drops of saturated solution 100 in 100 c.c. (about 01 per cent.) One .. About 43 minutes. 60 0-125 per cent. . 60 /f • • 19 minutes. 61 0-0625 60 /. 27 62 0-03125 60 w • • 50 63 0-0156 60 w 40 64 0-0078 60 « • 56 65 0004 60 // 111 „ 66 0-001 50 » 4^19 hours. 67 000075 50 „ . . 4^-19 „ 68 0-0005 50 // Alive 15 hours 48 min. later. 69 0-00025 50 tt • • w n 70 0'03125 50 /. 50 minutes. 71 0 004 '. 50 w • • About 8J hours. 72 0003 . i 50 /. „ 73 0002 50 M Between 8^ and 18J hours. 74 0-001 . I 50 It • . 19| hours. 75 0-00075 50 // • • About 30 minutes. 76 00005 60 Two .. One died between 8^ and 18J hours ; the other lived, and was alive and well four days later. It was intended to use trout-fry in experiments that were made to com- pare the action of tutin with that of other members of the same group, and to test the effect of remedies ; but the supply suddenly failed, so re- course was had to another small fish, known locally as the minnow, which aboiinds at certain seasons of the year in the waters of the Otago Harbour and Lake Logan. This fish [Galaxias attenuatus) is peculiar to the South Island of New Zealand, Tasmania, and Tierra del Fuego (33). It mea- sures 1-3J in. long, is equally at home in brackish and fresh water, and will live in a trough in the laboratory for weeks if fed on Liver and supplied with fresh running water. It is semi-transparent, and the heart can be seen beating. After a great many experiments it was found that the best results were obtained when three fish were used, and placed in a fairly wide (7-in.-diameter) enamelled bowl, containing 1,000 c.c. fluid. It was found necessary to almost completely cover the top of the bowl with a piece of wood, for if left uncovered the fish were apt to leap out. This happened several times, andjwas often more aggravating to the experimenter than 308 Transactions, disastrous to the fish, for if discovered within an hour or so, wiped clean,, and returned to the water it would recover completely. Three of these fish will live in 1,000 c.c. of water from thirty-six to forty-eight hours or more, and are apparently quite comfortable, even when the water is much fouled with their own excreta. Sollmann states that 0-001 per cent, picrotoxin is fatal to fundulus in five to nine hours. His specimens (5 cm.) were not much smaller than the minnows used in the experiments recorded here. He used only 150 c.c. of water to each fish, and admits that occasionally one of the controls would die. It is probable that the amount of water used by Sollman was too small, for in the experiments made by the present writer to compare the effects of tutin and picrotoxin, it appeared that in the early experiments, where a small quantity of water (200 c.c.) was used, death occurred in four hours when the concentration was 0-001 ; whereas in the later experiments, with three fish in 1,000 c.c. fluid, 0-001 was fatal to only one fish of the three in twenty-four hours. This shows the importance, when using fish in this way, of allowing a sufficient quantity of water. Symptoms. — The symptoms shown by the minnows when three were put together in 1,000 c.c. of a lethal percentage (0-005) of tutin were as follows : After two to four hours, with no symptoms, the fish began to swim near the surface of the fluid, and became excited in their movements, swimming vigorously about, and even leaping repeatedly out of the water. At this stage they were frequently observed to emit bubbles of gas from the mouth. This discharge of gas, and the inability to sink, point to a derange- ment of the function of the swim-bladder. Later they lose their power of maintaining the normal position, and swim about near the surface, turned on the side. Now and again they recover the upright position, and swim excitedly about for a minute or two, and then fall back on the side. Later on they lie at an angle with the surface of the fluid, often with the head down, and swim about feebly in this position ; and later still they lie on the side on the bottom of the dish, and the gill-movements are laboured. At intervals they spring up from this position, and swim round on the side, while appearances suggesting convulsions are seen — viz., bend- ing of the trunk, accompanied by shuddering movements. At death it was invariably noticed that the gill-movements ceased before the heart stopped beating. (For protocol of symptoms, see Exp. 108.) Table IV shows that under the above-mentioned experimental conditions a percentage of 0-001 was necessary to cause symptoms to appear, but was not necessarily fatal unless other deleterious conditions, such as too small an amount of fluid, were present {e.g., Exps. 77, 78, 79 in Table IV show- fatal results within six hours, but under improved conditions 0"0035 was fatal to only one fish out of three) ; while a percentage of 0-005 caused symptoms within a few hours, and was generally fatal to all three fish within twenty - four hours. Between these limits various results were obtained : thus in 0-0035 per cent, two of the three fish recovered and one died, while in 0-003 per cent, and in 0-004 per cent, two of the three died and one recovered. But in these experiments, Nos. 89, 91, and 95, tin dishes were used, and the water became rusty before the end of the experiments. In order to insure a lethal effect, the dose was therefore raised to 0-005 per cent., and experiments were made to test the effect of various reagents in increasing or diminishing the toxic power of tutin. The effect of tutin was also compared with that of picrotoxin. FiTC'HETT. — Physiological Action of Tutin. 309 Table IV. Effect of Tutin Solutions on Galaxias attenuatns. — Minimum Lethal Dose. Percentage Volume Number Time of Onset Time ^$ of ! of of of Result. of S'^ Tutin used. Fluid. Fishes. Symptoms. Death. •c.c. Hours. 79 0-0005 200 One 5^ hours . . Fatal 6 78 0-00075 200 // • * 5 f/ . . 6i 77 0001 200 // • ■ Not observed w • • 4 83 0-001 1,000 Three— (a) . . Slight symptoms at Not fatal 9^ hours , , (6) and (c) No symptoms j 87 0-00125 1,000 Three // . • ff 86 00015 1,000 Three— (a) .. (6) and (c) 1 hour No symptoms Fatal Not fatal If; 88 0-00175 1,000 Three— (a) . . (6) and (c) 4J hours . . No symptoms Fatal Not fatal n 90 0-002 1,000 Three // • • fi 89 0-003 1,000 Three (a) .. (b} .. 2f hours 9* Fatal ' j to all 1 7 12 (c) .. 10 „ 11-23 l{a) .. 4 Fatal H 91 0-0035 1,000 Three- (b) .. (c) .. Slight symptoms from 7 to 10 hours No symptoms Not fatal Ua) .. (b) .. 1(c) .. 3j3j. hours . . Fatal 12 95 0-004 1,000 Threes 8 „ .. // • • 84 Slight symptoms at Not fatal 12 hours 106 0-005 1,000 ((a) .. Three j (6) .. {(c) .. (la) .. 7i hours .. 7* 64 „ ... ] Fatal to all 12-22 12-22 24 21 hours . . Fatal 124-25 108 0-005 1,000 Three ^(6) .. i(c) .. H // • • 12 (106 used a 54 „ .. Not fatal second time) , (b.) Comparison of Action of Tutin and Picrotoxin. SoUmann's statement that 0-001 per cent, picrotoxin causes death in four to nine hours was tested by the improved method (see Table V, No. 85). Three fish were put into 1,000 c.c. of 0-001 picrotoxin at 11 a.m. Up to 8.30 p.m. no symptoms were seen, though the fish were under observation all day. At 8.30 they began to swim more frequently near the surface, and when seen next day one was dead, but the others were unaffected, and were returned to the trough at the end of twenty-four hours. A 0-001 per cent, of tutin (Exp. 83) showed almost similar results. Previous to this an experiment where 0.00075 per cent, and 0-0005 per cent, picrotoxin and the same strengths of tutin were tested gave doubtful results, because the amount of fluid was too small (Table V, Nos. 81, 82, 78, 79). In other experiments picrotoxin was compared with tutin in a strength of 0-004 per cent. All the picrotoxin fish died — two at twelve hours and one at 294 hours (Exp. 100) ; while of the tutin fish two died — at twelve hours and at eight hours and a half — and one recovered (Exp. 95). With a 0-005-per-cent. solution of picrotoxin all three fish died — viz., at 3| hours, at llf hours, and at 12f hours (Exp. 107) ; while tutin of the same strength caused death to all at 22|^ hours and at twenty-three hours (Exp. 106) : so it would appear that picrotoxin is more lethal than tutin in equal per- centages. 310 Transactions. Table V. Picrotoxin and Tutin compared. Exp. No. Percentage Volume Number Time of Onset Time of of of of Result. of Drug. Fluid. Fishes. Symptoms. Death. C.c. « Hours. 80 Piorotoxin, 0-001.. 200 One .. Not observed Fatal 4 81 Picrotoxin, 0-00075 200 K . . 5 hours /y • • 6 82 Picrotoxin 200 f/ • • IJ „ // ■ • 4 77 Tutin, 0-001 200 H • • Not observed „ 4J 78 Tutin, 0-00075 . . 200 // • • 5 hours tf • • 6i 79 Tutin, 0-0005 200 w • • 5 „ « • • 6 Control to the above fishes under the same conditions (200 c.c. fluid) showed symptoms of asphyxiation in four hours. Exp. No. Percentage Volume Number Time of Onset Time of of 1 of of Result. of Drug. Fluid. Fishes. Symptoms. Death. C.c. Hours. 85 Picrotoxin, 0001.. 1,000 Three 9§ hours Fatal to one 22 (about). 83 Tutin, 0-001 1,000 w 9J „ All recovered , , 100 Picrotoxin, 0-004.. 1,000 Three— (a) .. 3i „ 29i {b) .. 3^ „ Fatal to all ■ 12 (c) .. 6^ „ 12 95 Tutin, 0-004 1,000 Three— (a) .. 3| „ Fatal 12 (6) .. 8 „ // • • 8^ } (c) .. Slight symp- toms at 12 hours Recovered . . 107 Picrotoxin, 0-005.. 1,000 Three - {a) .. 11 hours . . ( 3* (b) .. Fatal to all - llf (c) .. 12| 106 Tutin, 0 005 1,000 Three— {a) .. 7J hours ] f 22^ (b) .. 6^ „ •Fatal to ain 23 (c) .. H . 1 1 22J 105 Picrotoxin, 0-0132 1,000 Three— ■h (a) .. n „ / 3 [b) .. c) .. ^^ . •Fatal to all- 6^ 2i It was then resolved to compare picrotoxin with tutin in equimoleciilar solutions. The molecular weight of tutin (Ci^HjoOy) is 336, and that of picrotoxin (C4 5HgoOi9) is 887; hence equal weights of tutin and picro- toxin contain by no means the same number of molecules. Accordingly two solutions were prepared, one of 0-005 per cent, tutin and one of 0-0132 per cent, picrotoxin ( 0-005 x 887 336 and the experiment was carried out as before, three fish (one large, one medium, and one small) being added to each bowl (Exps. 105, 106). The fish in the picrotoxin solution began to show symptoms first. The small fish came to the surface after fifty minutes, and in sixty-five minutes it was on its side. The medium fish also was much excited. In an hour and a half the large fish was found swimming FiTf'HETT. — Physiological Action, of Tutin. 311 near the surface and emitting air-bells, while at this time the other two fish showed quivering movements of the trunk. In two hours and three- quarters the small fish was dead. In three hours the larger one was dead, and the medium-sized one died in five hours. So that 0-0132 per cent, picrotoxin killed all the fish in five hours. Meanwhile the fish in the equi- molecular solution of tutin began to show symptoms at the end of three hours and three-quarters, which continued till late at night — twelve hours after the exj)eriment was begun. The next morning two were found dead (between twelve and twenty-two hours after the experiment was begun), and the last one (medium-sized) died at twenty-four hours (Exp. 106). So the result shows that in equimolecular solutions picrotoxin is more lethal than tutin. One must be cautious, however, in applying these results to the case of mammals. In fishes the swim-bladder regulation is disturbed both by picrotoxin and by tutin, and of the two, picrotoxin seems to have the greater influence, for air-bells are more frequently seen to be emitted by fish subjected to the action of this drug. The swim-bladder — of such para- mount importance in the case of fishes — has no analogue in mammals, and it is therefore quite probable that the lethal power of these poisons may be reversed in this class of animals. Indeed, the experiments on cats (Exps. 4, 168, 169, 171) justify this statement. (c.) Effect on Fishes of Tutin Solution that has been hydrolysed. It has been a constant observation in the case of both lower animals and of human beings that tutu poisoning is more lethal when the stomach is empty. This suggested the possibility of the toxicity of the tutin being- increased by the action of the hydrochloric acid in the stomach. Experi- ments on fishes were therefore undertaken to test this. To 8 or 10 c.c. of a 0-5-per-cent. solution of tutin an equal amount of 0-4 per cent, hydro- chloric acid was added, and the mixed fluid kept at a temperature of 37° C. for different lengths of time in difierent experiments. It was then exactly neutralised with a solution of soda of corresponding strength, and made up to 1,000 c.c. In the first experiment (Exp. 92) of this kind 7 c.c. of tutin solution was so treated (0-0035 per cent, tutin), and a control (Exp. 91) of a solution of untreated tutin in corresponding strength was used. In the hydro- lysed tutin solution one fish showed symptoms at three hours and three- quarters, which continued till it died, at seven hours and a half. Another began to show symptoms at eight hours and one-third, and died between ten and twenty-two hours ; while the third showed symptoms at nine hours, and died at 22| hours. In the control of untreated solution one fish showed symptoms at four hours and died at four hours and a half, and the other two, of which one showed symptoms from the seventh to the tenth hour, recovered. Another experiment of the same kind was then made, a slightly higher percentage of tutin being used — viz., 0-004 instead of 0-0035. Two test- tubes were taken, each containing 8 c.c. of a 0-5 per cent, solution of tutin. To one, A (Exp. 94), 8 c.c. of 0-4 per cent. HCl were added ; so that the total percentage of HCl in the fluid was 0-2. This mixture was kept at 37° C. for one hour, then neutralised and made up to 1,000 c.c. To the S'c.c. tutin solution in the other test-tube B (Exp. 95) the same amount of HCl was added, but it was immediately neutralised, and then kept at 37° C. for one hour, and made up to 1,000 c.c. In each of these two solu- 312 T ransactions. tions three fish were placed, and they were observed at frequent intervals during the day- In B (control), symptoms began in three hours and three- quarters in a fish which died in twelve hours ; and at eight hours in a fish which died in eight hours and a half. The third fish showed slight symp- toms when last seen at night, twelve hours after the experiment was begun, and was apparently quite well the next day. After thirty hours this fish was removed, the fluid filtered, and three other fish placed in the solution. This second group of fishes was affected as follows : When last seen at night, two hours after the experiment was begun, they seemed unduly excited, and next morning all three were dead — i.e., within sixteen hours of the commencement of the experiment (Exp. 98). (In order to test whether a second use of the solution would influence the result, a control of 1,000 c.c. water that had been used the day before was also filtered, and three fishes placed in it. These fish were quite unaffected at the end of the experiment, so that one may disregard the fact that the control solution mentioned above was used twice.) Table VI. Effect of Hydrolysis by 0'2 per Cetit. HCl on the Toxicity of Tutin. Exp. No. Strength of Tutin. Hydrolysed or not. Volume of Fluid. Number of Fishes. Onset of Symptoms. Result. Time of Death. Per Cent. C.c Hours. 92 0-00.35 Hydrolvsed 1,000 ■ Three— 30 min. at37°C. («) .. 3J hours ) Fatal ( u {b) .. 8i „ 1 *^° 10-22 (c) .. 9 „ ) all 1 22^ Three- 93 0-0035 Not hydrolysed 1,000 fa) .. 4 Fatal . . H. (control to 92) (6) .. (c) .. Slight symp- toms, 7-10 hours No symptoms Recovered Not fatal 94 0-004 Hydrolysed 1,000 Three— 1 hour at 37° C. [a) .. {b) .. (c) .. Three— 5 hours 8 „ Died . . Recovered 25J 28 97 0-004 Same fluid as 94, 1,000 a) .. 3 Died .. 16 filtered b\ .. Tciree — 16 „ No symptoms " 221 95 0 004 Control to above 1,000 («) •• 3^\ hours . . Died .. 12 (6) .. (c) .. 8 12 „ Recovered 8* 98 0-004 Same fluid as 95, filtered 1,000 Three Three — 2 Fatal to all 16 111 0 005 Hydrolysed 1,000 {a) .. 6| „ Fatal 13t 1 hour at 37° C. (b) .. 5i „ ■ to 1 all 8* (c) .. 5J „ 9^ Three— 106 0 005 Untreated 1,000 («) •• 7J „ Fatal 22J (6) .. (c) .. 6i „ .. to all 23 24 Now, with regard to the hydrolysed tutin (Exp. 94), to which the foregoing served as control experiments : In the first set of three fishes, one showed FlTCliETr.--Physio[u(/ical Action of Tulin. 313 symptoms at the end of five hours, and died in 25J hours ; a second showed symptoms at the end of six hours and a quarter, and died at twenty-eight hours ; and the third showed slight symptoms at the end of eight hours, and recovered. The fluid was filtered, and three fresh fishes introduced, and of these one died within sixteen hours, one at 22J hours, and one re- covered (Exp. 97). A third experiment (Exp. Ill) was made with U-()05 per cent, tutin in the same way. Symptoms appeared in two of the fish at five hours and a third ; these died at eight hours and a sixth and nine hours and a sixth respectively. The third showed symptoms at six hours and two-thirds, and died at 13f hours. Usually fish live in a 0-005-per-cent. solution of tutin for an average of seventeen hours. To summarise the results of these three experiments : Twelve fish were subjected to the influence of hydrolysed tutin (0-0035 per cent, to 0-005 per cent.). Of these, ten died at an average period of fourteen hours ; the other two showed symptoms, but recovered. In the corresponding control solutions, of the twelve fish, nine died at an average period of 16-9 hours two showed symptoms, and recovered ; and one showed no symptoms It would seem to follow that In^drolysed tutin is more toxic than tutin itself but the rise in toxicity is not great, and in marked contrast to the action which takes place in dilute alkali at corresponding strength. (r/.) Action of Alkalis on Tulin. Attention having been arrested by the fact that animals poisoned by tutin are frequently reduced to a state of coma, which may possibly con- tribute towards a fatal termination, the use of alkahs as a remedial agent suggested itself. Hughes had found that lime destroyed the activity of the tutu poison, and Easterfield and Aston were unable to recover tutin after a solution treated with lime had been evaporated to dryness. Table VII. Effect of Alkali on the Toxicity of Tutin. Exi). Percentage Treatment by Volume of Fluid. Number of Fishes. Time of Onset of Symptoms. Result. Duration of No. of Tutin. Alkali. Experi- ment. C.c. Hours. 96 0-004 Treated with 0 2 percent. NaOH at 37° C. for 1 hour 1,000 Three No symptoms All lived 30 99 0-004 Ditto .. 1,000 " " " 27 101 0-005 Treated with 0-2 percent. NaOH at 37° C. for 20 minutes 1,000 " " „ 25 102 0-005 Ditto, for 40 mi- nutes 1,000 " " '■ 25 109 0005 Ditto, for 10 mi nutes 1,000 " " 30 112 0 005 Ditto, for 5 rni- 1,000 ,, ^^ „ 26 nutes The experiments were done in the same way as in the case of HCl : 10 c.c. of a 0-5-per-cent. solution of tutin was rendered alkaline with the solution 314 Transactio?is. used in the foregoing experiments to neutralise the weak liydrochloric acid. The alkaUnitv used was equivalent to 0-2 per cent. HC'l. or a little over 0-2 per cent." It was found (Exps. 96, 99. 101, 102. 109, 112) that tutin solution kept at 37° C. in the presence of that amount of alkali completely lost its toxic power. In the first experiment the time allowed for the alkali to act on the tutin was one hour, and the three fish that were subjected to the action of the solution were unaffected after thirty hours. The fluid was filtered and three other fish introduced for twenty-seven hours, but without effect. In other experiments the time allowed for the alkali to act upon the tutin was shortened successively to forty minutes, twenty minutes, ten minutes, and five minutes, but the result was the same in each case — the tutin had completely lost its toxic power. In this connection the following experiment on a cat may be cited (Exp. 113) : 8 c.c. of a 0-5-per-cent. solution tutin was treated with 1 gram of lime [CalOHg)] for one hour at 37° C, and thereafter for one day at room-temperature. The lime was removed by passing CO2 and filtering, and the fluid was evaporated to about 2 c.c, and injected under the skin of a cat weighing 2-4 kilograms. It displayed no symptoms, and remained well. (c.) Influence of " Surviving '' Organs on Tutin. In considering the explanation of the relative immunity of birds to tutin poisoning by oral administration, it was suggested {vide ante) that the inter- position of the liver in the usual path of absorption in mammals might account for some increase in the toxicity of the tutin in their case. To test the influence of the liver-substance on tutin, an experiment was carried out as foUoW'S : A rabbit was killed by chloroform, a canula was tied into the aorta, and the blood-vessels washed free of blood by a stream of warm saUne. The liver and kidneys were rapidly excised, 9 grams of each weighed out, minced, and bruised rapidly in a \varm mortar. To each mass 10 c.c. of a 0-5-per-cent. solution of tutin in normal saline was added. The mixtures, in small wide beakers, w^ere placed in the oven at 37° C. for one hour. An equal volume of absolute alcohol was then added, to stop further action. The mixtures were then evaporated on a water bath, and kept there for some hours to coagulate the proteids. A watery extract of each was then made, filtered, and made up to 1,000 c.c. with tap-water. Three minnows were placed in each of these solutions, and the results were as follows : — Liver and Tutin (Exp. 103) : One fish showed symptoms at two hours and a third, and died in five hours and a half ; one showed symptoms in two hours and a third, and died in six hours ; and one showed symptoms in four hours and a half, and died in seven hours and three-quarters. Kidney and Tutin (Exp. 104) : One showed symptoms at an hour and a half, and died in four hours and a half ; one showed symptoms at four hours and a half, and died in seven hours and three-quarters ; and one showed svmptoms in four hours and a half, and died in twenty-seven hours. The course of events in the latter case is just similar to that of a 0-005- per-cent. solution of tutin, so that we may suppose that here the tissue had no effect on the tutin ; but, on the other hand, it is difficult to avoid thinking that the liver-substance increased the toxicity of the tutin, 6. Action on Insects. Insects are susceptible to the action of the poison. Weak solutions (0-1 per cent.) have no influence. A number of flies lived in perfect health FiTCHETT. — Phi/siological Action of Tut in. 315 for a week on a solution of cane sugar in 0-1-per-cent. solution tutin (Exp. 115) ; but a 0-5-per-cent. solution quickly produced symptoms, and caused death in half an hour or so (Exp. 116). The symptoms were very like those that characterize the action of the poison in higher animals — namely, an initial lethargy, followed by isolated tonic spasms of the wings and legs, exactly resembling the appearance met with in pigeons in the early stages of poisoning, when one or other wing is extended in rigid spasm for a moment ; then marked clonic spasm of the wings recurring at intervals, and finally general convulsions, in which the insect tossed and buzzed about until exhausted. In the latest stages the flies lay on their backs, showing only occasional movements of the legs. After death, distention of the abdomen was an invariable finding, and in the case of a blowfly the exudation of a considerable drop of clear fluid from the proboscis occurred. 7. Action ox Larv^. (Exp. 117.) The eft'ect of the poison on maggots was tested by placing some mince that had become infected by blowflies in solutions of tutin of different strength for one hour, and then draining off the fluid. The experiment was controlled by a portion of the mince being placed in normal saline for the same period. On the day following, the maggots in the control had hatched out, and were very active ; but in the mince subjected to the action of a 0-5-per-cent. solution tutin no movement was seen, and only one or two larvae were found moving in the mince that had been soaked in tutin solutions of lesser strength. Experiments that were made on full-grown maggots showed that con- finement for forty-eight hours in tutin solutions of strengths graded up to 0-05 per cent, had apparently no influence. As immersion in a 0-05-per-cent. solution is about equivalent to a dose of 500 mlgm. per kilo, or 0-5 gram, tutin is seen to be very inactive. 8. Action on Molluscs. (Exp. 11-1.) Two cockles of about the same size were placed one in sea-water and the other in a 0-5-per-cent. solution of tutin in sea-water, freshly prepared. Equal volumes of fluid were aUowed. The cockle that had been placed in the tutin solution, in five minutes opened its shell and extruded its body. If touched it immediately withdrew, but came out again at once. It kept opening and closing its shell, but did not withdraw its body as the valves came together. It continued Uke this for twenty- four hours, responding more sluggishly to a touch as time went on, and then died. The control meanwhile had displayed no symptoms, but behaved in exactly the way the other had done when it, in turn, was placed in the tutin solution, and it also died. 9. Action on Infusoria and Au(ebm. The action on infusoria and amoebae was examined in the following way : — A drop of hay-infusion, containing infusoria, amoebae, monads, and bacteria, was placed on a slide ; a drop of 0-1-per-cent. solution tutin was added, and the specimen observed for an hour. A drop of the infusion to which nothing had been added was used as a control. Another drop to which a drop of normal saUne had been added was used to test the influence 316 Transactions. of tlie saline in which the tutin was dissolved ; and a fourth drop, to which a drop of a 0-1-per-cent. solution of quinine-sulphate had been added, was used for the sake of comparison (Exp. 118). In fifteen minutes no para- moecia were found moving in the quinine preparation, but monads were still in motion. In the three other specimens no change was observed. In thirty minutes all movement had ceased in the quinine preparation. In the tutin preparation paramoecia could still be seen moving, but their movements seemed to be somewhat irregular ; amoebae, bacteria, and monads were still moving. In one hour one or two paramoecia could still be seen moving in the tutin preparation ; they were by no means so numerous as at first, and rather difficult to find. Many of the monads were as active as ever, and amoebae were still throwing out pseudopods ; but the preparation did not present the same appearance of general activity that it did at first. The saline preparations and the control were as active at the end of the experiment as they were at the beginning. A further experiment (Exp. 119) was made by covering a drop of hay- infusion with a cover-glass, and then placing a drop of 0-1-per-cent. tutin solution on the edge of the cover. It was observed that such paramoecia as swam out into the drop of tutin solution remained in that drop, displayed irregular movement, and in a few minutes came to a standstill, and appeared to undergo internal disintegration, whicli reduced them to unrecognisable masses. The experiment was repeated with a drop of a 0-5-per-cent. solu- tion tutin in distilled water, with similar results (Exp. 120). It would appear, therefore, that paramoecia are injuriously affected by the poison, but not in so great a degree as they are by quinine. On amoebae, dilute solutions (about 0-05 per cent.) have very little influence. Monads are affected in a lesser degree than paramoecia. 10. Action on Bacteria. (Exp. 121.) This was tested by placing pieces of fresh mince in test- tubes containing solutions of tutin of different strength (0-1 to 0-5 per cent.) and a piece in a test-tube containing normal saline alone. The tubes were left open to the air for twenty-four hours, and then corked and placed in an incubator at 37° C. Two days later the tubes were examined, and it was found that the tube containing saline was very offensive, but the tubes containing tutin solution were not at all offensive, and smelt rather like stomach-contents. When subjected to microscopic examination, it was found that all the solutions contained bacteria, but in the slide prepared from the normal saline the bacteria were very much more numerous, and showed a greater variety of form and size. It Avould appear, therefore, that tutin has a deleterious action on certain forms of bacteria, but not on all. That some forms of bacteria are certainly not affected by tutin is shown by the following observation : A 0-5-per-cent. solution of tutin in normal saline which had been allowed to stand for six months in the laboratory was examined microscopically, and found to contain fairly numerous large motile bacilli resembling B. suhtilis. A green growth that had developed and formed a layer at the bottom of the bottle was found to consist of small rounded yeast-like cells tinged with chlorophyl. 11. Action on Yeast. The action of tutin on the fermentation of glucose by yeast was studied in a few experiments (Exps. 122, 123, 124). It was found that fermentation FiTCHETT. — Physiuloyical Action of Tut in. 317 proceeded vigorously in the presence of even 04 per cent, tutin. Some slight differences in the rate of fermentation that were noted were probably due to differences in the amount of yeast added. (For details of experi- ments, see protocols, Exps. 122, 123, 124.) 12. Germination of Seeds. The action of tutin on the germination of seeds was tested by soaking mustard-seeds in solutions (in normal saline) of various strengths (0-1, 0-2, 0-3, 04, and 0-5 per cent.) for twenty-four hours (Exp. 125). The seeds were then sown on pieces of felt in separate tin boxes, appropriately labelled, and kept moist with water. An equal number of seeds was sown on each piece of felt, and the experiment was controlled by seeds that had been soaked for the same length of time in normal sahne. The day following, all the seeds had germinated, and they were therefore replaced in their respective tutin solutions for a further period of twenty-four hours, and then sown again. During the next week the progress made by the seedlings was observed, and the effect of the tutin on their development noted. It was found that the seeds progressed more or less in order of the weak- ness of the solutions in which they had been soaked : thus, the growth of those that had been soaked in normal saline, in 04 per cent., and in 0-2 per cent, tutin was the most vigorous, while those that had been soaked in 0-3, 04, and 0-5 per cent, made slow progress, and all the seedlings in these lots did not continue to grow. In a fortnight, however, little difference was to be noted in any of the seedlings that had developed at all, one or two of the 0-5-per-cent. seedhngs that were growing being as well developed as those that had been soaked in saline. This result may possibly be due to the effect previously noted on bacteria, certain forms of bacteria being necessary to the growth of plants. From experiments on invertebrates, bacteria, &c., it may be inferred that tutin is toxic to any given form of life in proportion to its complexity of organiza- tion. Wherever a nervous system is sufficiently developed, the toxic action is greatest; but that it has some injurious influence on primitive protoplasm may also be seen from its effects on paramoecia, bacteria, &c. 13. Action of Tutin on Tissues. From the symptoms observed when studying the general action of the poison on mammals, it seemed very evident that the nervous system was the part chiefly affected. Nervous tissue will be considered later, and the action of tutin on otlier tissues will be recorded first. (a.) Action on Primitive Protoplasm. As is shown in Exp. 118, tutin, as compared with quinine, is not a strong protoplasmic poison. That it has some deleterious action on living proto- plasm is shown by the experiments on putrefactive bacteria, on the germina- tion of seeds, and on paramoecia (Exps. 121, 125, 119), though it is doubtful if the action here is more than might be exerted by any foreign substance. (b.) Ciliated Epithelium. The action on ciUa was tested in the following way : A few bars from the gill of a cockle were placed on a slide in a drop of sea-water, and ex- amined with a power of 80 diameters. In the first experiment, the prepara- tion was covered with a cover-glass, but in the later experiments cover- 318 Transactions. glasses were not used, in order to allow of ready interchange of O2 and COj. The results are shown in Table VIII (Exps. 126 to 134 inclusive). Table VIII. Action of Tutin on Cilia. Exp. No. Source of Material. Strength of Tutin. Effect. Time. Eemarks. Per Cent. 126 Cockle-gill Same preparation 0-1 in saline 0-2 0-3 No change Retarded (?) Slowing Ceased 7 min. 4 „ 1 „ 8 „ Control specimens - in normal saline continued active. 127 Cockle-gill 0-3 Slower Ceased 1 „ 5 „ 128 0-2 Practically ceased 7 „ Movements restored by 1 in 1,000 KOH. 129 // 0-2 No change 9 „ Same preparation 0-3 „ Less active 10 „ // 0-5 Still moving 15 „ 130 Cockle-gill 0-2 Slowing 7 „ Accelerated by infu- sion with sea- water. ' Slight retard- 5 „ 131 Rock-oyster gill . . 05 ation (?) Still active Exagger- 1^ hours. 2 min. 132 Cockle-gill 0-5 ated (?) Still active 1^ hours. 133 Ciliated epithe-' Hum of frog's gullet 01 0-5 No change 1 hour. 1 „ (Exp. 13-1.) The rate of progress of a small fi'agment of cork along the surface of the gullet was noted before and after applying tutin (0"3 per cent. in saline). Average rate before = 50'4" for 1 cm. travelled ; average rate after = 34-8" for 1 cm. travelled. The method presented many difficulties, as it is impossible to keep the fi'agment moving on the same line each time, and the mucus secreted clogs its movements. From these results it is impossible to draw a definite conclusion, for although in some specimens taken from sea-water animals the ciliary action ceased on the application of tutin, in other specimens from the frog's gullet tutin had little or no action. (c.) Action of Tutin on Striped Muscle and Nerve-terminations. This was tested by determining the strength of stimulus just sufficient to cause contraction of a nerve-muscle preparation before and after the application of tutin. The preparation (gastrocnemius - sciatic) was made from the frog. An induction-coil with one Daniell cell and mercury-key was used. The muscle in each case was placed first in normal saline (0-75 per cent.) and the strength of the minimal stimulus determined. The tutin solution was then substituted for the saline, and the excitability tested from time to time. Four experiments were made (Exps. 135 to 138 inclusive). In three of these the one muscle was placed in 0-025, 0-05, and in 0-5 per cent, tutin solution, while the other muscle was placed in normal saline. In another experiment the muscle of one preparation was placed in 0-5-per-cent. solution tutin, and the nerve of the other in 0-5-per-cent. tutin. (Exp. 136). FiTCHETT. — Physiological Action of Tutin. 319 In the first experiment (Exp. 135)^0-025 per cent, tutin — there was a diminution in excitability : thus, the muscle in saline contracted with the coil at 18 cm., three hours after the experiment began, while the corre- sponding muscle in tutin contracted only at 15 cm. Where 0-05-per-cent. solution tutin was used (Exp. 137) the muscles were equally excitable after two hours, but the muscle in the tutin had been the more excitable of the two before immersion in the tutin. Thus, before tutin was apphed it contracted at 30-5 cm., and two hours after the application of tutin at 25-5 cm., while the control contracted at 25-5 cm. and at 25 cm. Another experiment where the muscle was placed in 0-05-per-cent. solu- tion tutin gave the following results (Exp. 138) : Before immersion in tutin solution — A contracted at 36 cm. ; B (control) contracted at 32 cm. Two hours after immersion in tutin solution — A contracted at 21 ; B con- tracted at 23. In the experiment with 0-5-per-cent. solution tutin (Exp. 136) the minimal stimulus before the apphcation of tutin for A was 28 cm., for B 34 cm. The muscle of B (control) and the nerve of A were then placed in the tutin solution, and an hour and a quarter afterwards A contracted at 33 cm. and B contracted at 27-5 cm. (For details of these experiments, see protocols.) The inference to be drawn from these few experiments is that tutin has no striking action on nerve or muscle fibre ; but there seems to be a diminution in the excitability in the muscle placed in tutin solution, due either to an action on the nerve-terminations or to an action on the muscle fibre. This would help to explain the weakness and loss of tone seen in the later stages of tutin poisoning, especially well seen in frogs. It is possible that the action is one on the nerve-endings, for instances are known of a poison {e.g., strychnine) acting as an irritant to nerve-cells, and having at the same time a paralysing action on motor-nerve endings. Nussbaum (27) states that picrotoxin in small doses stimulates, and with slightly higher doses depresses, the activity of the peripheral nerve-termi- nations. The same may be the case with tutin. 1-1. Action on the Different Systems. (a.) Alimentary System. Salivation is a marked feature in animals poisoned by tutin. It is an early symptom, and usually precedes the vomiting, though it may be present when vomiting is absent, as in Exps. 1 and 2. It is most profuse where the dose is large, and in these cases is a source of danger in the later stages by obstructing the respiratory passages. As a rule, it diminishes when vomiting has occurred, and is not a marked feature in those animals (rabbits and guinea-pigs) that do not ^'omit. Probably, therefore, it may be an exaggeration of the saUvation which usually precedes the act of vomiting. The saliva is thick and ropy, and hangs from the mouth in long tenacious strings. 8ahva of this consistence suggests stimulation of the sympathetic. Vomiting is also an early symptom. It is not an invariable symptom, being present in only two of the cats and in three or four of the pigeons experimented upon. It is more hkely to occur if the dose be small. The salivation and the vomiting could both be explained as due to stimulation of the vomiting-centre in the pons. That it is due to stimu- lation of the centre is shown by the fact that it occurs when the poison is 320 Transactions. given hypodermically. But in ordinary cases of poisoning by the tutu plant there may be irritation of the gastric mucosa as well. Christie's assertion (11) that tutin is excreted by the stomach, and so causes vomiting by local irritation, is unsupported. No tutin could be extracted from the gastric and small-intestine contents of a rabbit which had been killed bv intravenous injections of large doses of tutin during a blood-pressure experiment. Stomach. — In cases of herbivora poisoned by tutu, accumulation of gas in the stomach is a marked feature. This is probably diie to the rapid fermentation of the leaves ingested, though possibly it may be due, in part, to air swallowed during the convulsions. To test the fermentability of tutu-leaves, a mash of minced leaves with a little water was placed in an incubator at 40° C, and examined after the lapse of an hour. On stirring the mixture it was seen to be permeated with bubbles of gas, but it was not determined how far this was due to the expansion of imprisoned air. In the experiments with the pure substance, distension by gas was not observed. Pure tutin and artificial gastric juice when incubated in a fer- mentation-tube gave no appearance of gas-development. The action of hydrochloric acid in hydrolysing tutin has already been referred to under " Fishes." It was found that the toxicity was slightly increased. Intestines. — The action on peristaltic movement was not investigated experimentally, but from observations made on animals killed by tutin, where the abdomen was opened immediately, it was clear that there was no diminution of peristaltic movement. That it was even increased was inferred from the frequency with which defsecation occurred. The stools were often loose, and were expelled with some violence. {b.) HcBmopoietic Si/stem. In one experiment, where a rabbit received a fatal dose of tutin and died in one hour, blood-films were taken before the injection of tutin and just before death (Exp. 139). The only point of difference seemed to be that the leucocytes appeared fewer in number after tutin. They seemed to be quite normal in regard to granules and staining-power. (c.) Circulatori/ and Respiratory Systetns. Previous observers have noticed that the tutu poison has no depressing influence upon the circulation. Christie (11) found that the heart con- tinued beating after the respiration had ceased. In one of his experi- ments (on a cat) he opened the thorax immediately on the cessation of all movement, and observed the heart to beat for twenty-two minutes after the last respiratory gasp. In his own case, where he took 9 grains of an extract made from the leaves, the pulse-rate rose to 102. and this observa- tion led him to conclude that the action of the poison was to accelerate the beat of the heart. In attempting to bleed poisoned animals by open- ing veins and by slitting the ears he found that the blood did not run readily, and concluded that the arterioles were contracted. He noticed, also, what had been observed previously in cases of accidental poisoning — that at first the respirations were increased in frequency and in force, and that later they became feeble and irregular, and finally ceased before the heart stopped beating. FiTCHETT. — Physiological Action of Tut in. 321 Marshall (24) found that tutin diminished the number of heart-beats and increased the frequency of respiration. As coriamyrtin belongs, pharmacologically, to the picrotoxin group, and is therefore closely allied to some of the decomposition-products of digitalixi — e.g., digitaliresin (30) — it was expected that tutin, which is so closely related to coriamyrtin, might show the tonic action on the heart that is characteristic of the digitalis bodies. In frogs and in mammals, where the heart was examined after the breathing had ceased, it was found invariably to be still beating. In one experiment on a cat (Exp. 153) the heart-beat was distinctly audible with the stethoscope for two minutes and a half after respiration had ceased. As it had been observed that tutin has apparently no action on_ striped muscle (Exps. 135 to 138), and as no proof was forthcoming that it has any action on unstriped muscle, it was not considered likely that it would manifest any direct action upon cardiac muscle. As it might, however, have some action on the extrinsic and intrinsic nervous mechanism of the heart, it seemed best to begin the study of its action upon the circulation by observing its effect upon the heart of a pithed frog, where one has to consider muscle and intrinsic ganglia only. A number of experiments were undertaken to determine this. Tracings* of the frog's heart-beat were taken in the usual way with a lever arranged to write against a blackened revolving cylinder. In some cases the tutin solution was painted on the surface of the heart ; in others it was injected into a vein or into the heart itself. The results obtained show that the rate of the beat was slightly diminished : thus, in Exp. 140 the rate fell from 37 to 35 beats per minute : in Exp. 141 from 32 to 30-8. then to 28-8. and then to 26-4 per minute ; and in other experiments from 20 to 14 and from 20 to 16. After injection of tutin the force of the heart-beat was increased, and the beat was not impaired even with a concentration of tutin solution greater than could possibly be reached by absorption of the poison from the stomach in cases where the plant has been eaten. An irregularly beating heart was generally improved, the beat becoming regular. So that it may be concluded that tutin has a purely beneficent influence on the heart's contraction. Action on Mammalian Circulation. — This was studied by taking tracings of the blood-pressure from one or other carotid arte^ry, and noting the effect of injections of tutin solution into the jugular vein. The animal was anaes- thetised (chloroform and paraldehyde) during the experiment, and was not allowed to regain consciousness. It was found that injections of tutin solution (0-5 per cent.) caused a rise of pressure : thus in Exp. 143 the initial pressure was 3 in. ; in the course of an hour, during which the animal received nearly 10 mlgm. tutin, the pressure rose gradually to 4|in."ln some cases the vagi were divided before the drug was injected, but without affecting the result. The rate with which the blood-pressure rises is proportional to the size of the dose given. In one experiment (Exp. 145), where the abdomen had been opened and its contents handled, a reflex cardiac inhibition seemed to be set up, for the tutin injection in this case caused a marked fall in pressure, which was followed by a rise on division of the vagi. It appears, therefore, that tutin increases the * As the tracings had to be sent to Edinburgh with the original thesis, it is im- possible to reproduce them here, and this portion of the work has therefore been sum- marised, and technical details have been omitted. 11— Trans. 322 Transactions, excitability of the medullary centres, and the stronger reflex effects from these usually lead to a rise of blood-pressure ; but in cases where some reflex cardiac inhibition already obtains, this is increased by tutin, and a fall in pressure results. That tutin acts specially on the centres in the medulla was also shown in several experiments where Traube-Hering curves and Cheyne-Stokes type of respiration occurred simultaneously. When twitching and general convulsions set in, the blood-pressure curve became markedly irregular, due probably to mechanical obstruction to the flow through the vessels. The action of tutin on the vagus-endings in the heart was investigated. The strength of stimulus just necessary to inhibit the heart slightly and cause a fall of blood-pressure was determined both before and after the injection of tutin. No marked difference was obtained, so it was con- cluded that tutin has no influence on the excitability of the nerve-ending in the heart. In some of the later experiments a spring manometer was used to mea- sure the blood-pressure instead of the ordinary mercurial manometer. This, by recording each heart-beat on the tracing, enabled the rate to be accu- ratelv determined. It was found that there was no increase, but in rabbits the rate is already so high that one could hardly expect much change. A curious periodicity in the heart's action was observed in spme cases towards the end of the experiment when the animal was dying, one or two beats being missed at each inspiration. The explanation of this was not at first clear, but in a subsequent experiment on a cat (Exp. 153), where the heart was auscultated as the animal was dying and breathing in the way shown in the tracing, it was noticed that towards the end of each in- spiration the heart missed two or three beats. The explanation of this seemed to be that as the respirations were infrequent and deep, and the respiratory passages obstructed by quantities of mucus and saliva, the deep forcible inspiration created so much negative pressure in the thorax that the heart was unable to beat until the pressure was relieved by expira- tion. That the variation was due to respiratory influence, and not to any action of the drug upon the circulation, was shown in the case of this cat by the fact that when respiration had ceased the heart continued to beat regularly for two minutes and a quarter. With regard to Christie's statement that the arterioles are contracted, no direct experiments were made, but some perfusion experiments on frogs showed that there was no marked or constant change. Further, the action on the heart is sufficient to account for the rise in blood-pressure. Were the arterioles also constricted, one would expect a much higher rise than occurs. Any influence that tutin does exert on the calibre of vessels is exerted through the vaso-motor centre in the medulla, as seen in the Traube-Hering curve already mentioned. Action on the Respiratory System. — The rate and amplitude of the respiratory movement is markedly increased by tutin. After the first injection in the anaesthetised animal the rate may be doubled. During convulsive seizures the spasm of the respiratory muscles is very marked, and respiration appears to be brought to a complete standstill — e.g., in a cat (Exp. 3), during an interval of four minutes and a half, no visible or audible sign of breathing could be noticed. Doubtless this is a frequent cause of death in animals poisoned by a large absorption of tutin. That respiration ceases before the heart was a constant observation. It was seen in fishes and in all animals where such an observation could be made. FiTCHETT. — Physiological Action of Tutin. . 323 Breathing of the Cheyne-Stokes type occurred in some experiments, the climax of the period of respiratory activity corresponding to the highest point of the Traube-Hering curve, which appears simultaneously. {d.) Urinary System. Micturition was a marked feature in cats poisoned by tutin. It occurred voluntarily several times before convulsions occurred, and during the con- vulsions (and this is true also of rabbits and gmnea-pigs) involuntary discharges of urine occurred. In the majority of cases the bladder was found distended after death, even where a free discharge of urine had taken place during the convulsions. This points to an increased secretion of urine. Attempts were made to estimate the rate of flow in anaesthetised animals (Exps. 144, 145). but without satisfactory results. This increased secretion pointed to the possibility of tutin being elimi- nated in the urine, and so an attempt was made to recover tutin from the urine of poisoned animals. The urine was collected by incising the bladder after death. It was evaporated to dryness and exhausted with ether, but no crystals of tutin could bei detected on evaporating ofT the ether. The residue from the ethereal solution was in one case dissolved in saline and injected under the skin of a frog (Exp. 151), but with negative results. The urine was in several cases examined for abnormal constituents, but none was found. {e.) Genital System. Many of the animals experimented upon were pregnant females in different stages of pregnancy, but in no case was abortion observed, although the animal was under the action of the poison long enough for it to occur. (/.) Nervous System. The symptoms that appear in animals poisoned by tutin point clearly to the central nervous system as the part of the body that is specially affected by the action of the poison. The two cardinal symptoms are convulsions and a dulling or blunting of the mental faculties that in the early stage makes the animal appear dazed and stupid, and in the later stages passes into actual coma. Convulsions. — The convulsions are obviously of central origin. They bear a close resemblance to an ordinary epileptic fit, which is generally held to originate in the cortex. Whether the tutin convulsions originate in the cortex or not, it is certain that the nerve-cells in the basal ganglia, pons, medulla, and cord are profoundly affected. This is shown by the action on the vomiting centre, respiratory centre, and cells of the cord. Among the first symptoms to appear are twitching of the ears, blinking of the eyes, and movements of the lips. These are followed by jerking of the head and movements of the fore and hind limbs. These movements may be attributed to irritation of the cells of either the upper or the lower motor neurones. In order to determine more accurately the site of action the follo^^'ing experiment was made :• — (Exp. 152.) The right cerebral hemisphere was exposed in a cat and a large dose of tutin injected hypodermically. When general convulsive movements had developed, the right cerebral hemisphere was removed. Now, had the convulsions been cortical in origin, one would expect them to have ceased on the left side of the body ; but they continued as before. 324 Transactions. affecting botli sides equally. The left hemisphere was then removed, but the movements were unaffected, and continued on both sides equally. So it may be concluded that the convulsions may originate in the cells of the lower neurones, or, at any rate, that the upper neurone is not necessary for their development. Further observations made in this experiment lend support to this suggestion. After the cerebrum had been removed, the cord was divided at the level of the fifth dorsal vertebra. Four minutes after- wards tonic and clonic spasms of the hind limbs were observed, and con- tinued intermittently for a quarter of an hour. As the cells of the cord were now completely cut off from the higher centres, these movements must have originated in the neurones of the spinal cord itself. Post Mortem. — The chest was opened just after all respiratory move- ment had ceased, and the heart was seen to be still beating. The bladder was full. The cerebral hemispheres were found to be entirely removed. The cord at the seat of section was examined, and it was found that division was complete, but there had been some crushing of the tissue on either side of the section, and the dura mater was still intact. Although satisfied that division was complete, it was thought that the crushing of the cord may have caused irritation, which might possibly be held to account for the movements observed in the hinder part of the body. It was resolved, there- fore, to repeat the experiment. This was done as follows : — (Exp. 153.) A cat was chloroformed, the cord exposed, and completely and cleanly divided in the mid-dorsal region. Five mlgm. of tutin were then injected into the peritoneum, and chloroform anpesthesia discontinued. Ten minutes later no reflex could be elicited from the left hind foot, while the left fore foot responded normally. Fifteen minutes after the injection of tutin twitching of the ears and jerking of the head began, and became very distinct at twenty-four minutes. Two minutes later a convulsive movement of the fore part of the body occurred, and was accompanied hy a movement of the tail. These convulsive movements of the fore part of the body continued for nearly an hour, and the animal died an hour and seven- teen minutes after the injection of tutin. About half an hour after the cord had been divided and tutin injected, reflexes could be obtained from the hind limbs ; and ten minutes later a stimulus applied to one hind limb caused movements of both. During the last half-hour of life the move- ments of the tail became more and more marked. They generally appeared just at the beginning of each convulsive seizure of the fore part of the body, but they also occurred independently. Sometimes the whole tail was moved from the root, at other times there was only a slight movement of the tip. One hour after section of the cord convulsive movements (tonic and clonic spasms) of the hind limbs occurred, and were accompanied by defaecation and erection of the hairs of the tail. These convulsive move- ments were frequently repeated. By this time the fore part of the body had become almost quiescent, but the spasms of the hind limbs increased in severity until death. It was in this experiment that the heart was observed to beat intermittently during the long-drawn, obstructed inspira- tions. When respiration had ceased, it continued to beat regularly for two minutes and a quarter. The conclusion to be drawn from these two experiments is that the con- vulsions that occur in tutin poisoning may originate in the lower centres of the pons, medulla, and cord. The action on the cord is a late appearance, and this corresponds to the finding of Gottlieb (28) that picrotoxin can elicit convulsions below a section of the spinal cord, and that these appear later FiTCHETT. — Physiological Action of TuHn. 325 in the hinder part of the body. This result does not agree with the state- ment made by Marshall (24) that the spasms in tutin poisoning are not produced below a section ol the cord. Like other convulsants, tutin raises the excitability of the reflex arc. This is shown in the last experiment, where crossed reflexes could be obtained soon after section of the cord. This rise in excitability might explain the severity and frequent repetition of convulsive seizures when once they begin, for it is known that in strychnine poisoning, where the reflex excitability is raised, the afferent, probably painful, impulses coming from the convulsed muscles originate further convulsions, and thus a sort of vicious cycle is set up. In this connection it may be noted that it has long- been known to farmers that if " tooted " sheep are left undisturbed no symptoms may appear ; but once the symptoms are initiated — say, by the bark of a dog — they continue, and are from the outset severe. The ex- planation given above would account for the apparently sudden onset of severe symptoms. It seemed of interest to determine whether the reflex time was shortened. Florence Buchanan (29) and others found that strychnine in small doses did not perceptibly shorten the reflex time. It was impossible in this case to use the same elaborate method, so recourse was had to the simple but less accurate method of Turck. The results of the experiments, with details of the method, are given in the protocols, but they may be shortly summarised here. Six experiments were made. In three of these (Exps. 154, 156, 157) the reflex time was shortened from 6 to 4, from 6 to 5. and from 6-1 to 3 respectively ; while in three others (Exps. 155, 158, 159) the time was lengthened from 8 to 12-2, from 8-3 to 22, and from 8-5 to 44. From these results it will be seen that no definite conclusion could be drawn. The one thing that did appear in these experiments was that the amount of movement was increased after the injection of tutin, the stimulus as a rule now causing general movements of the body. Thus, though the effect of tutin upon the reflex time remained doubtful, its effect in increasing reflex excitability seemed to be clear. In frog 157 the injection of tutin caused a typical convulsion, and in this case it was found that the optic lobes had not been pithed. In cases where the pithing destroyed all parts but the cord no convulsions occurred. Although this dift'ers from what was found in mammals where tutin pro- duced ,spasms below a section of the cord, it agrees mth Gottlieb's (28) finding that in picrotoxin poisoning m frogs convulsions did not occur below a section of the cord. The second important svmptom of tutin poisoning is the comatose condition that is so invariable an accompaniment. This occurs in various degrees according to the dose, and it deepens as the case advances. In the recorded cases of poisoning of human beings, referred to above, complete loss of consciousness and subsequent loss of memory was frequently observed. Loss of memory appears to occur also in lower animals, for shepherds have observed that a " tooted " lamb which has recovered does not know its own mother, and the ewe may be seen following her lamb and striving to excite recognition. Another proof that abrogation of sense-perception obtains is the marked absence of any evidence of pain. The animals utter no cry of pain, although the convulsions are very severe, and would, were this condition not present, be most painful. 326 Transactions. From the examination of sections of the cerebrum, meduHa. and cord there is evidence of great congestion of these parts in tiitin poisoning. The central nervous system was examined in several cases after death, and congestion of the membranes was found in all. In one case the grey matter of the cord when seen on section was distinctly reddish. Pieces of cord, medulla, and cerebrum were fixed in 8 per cent, formol. and sections were made and stained by Nissl's method, and also by Muir's eosin and methv- line-blue method. On microscopic examination the Nissl granules showed no obvious change, but there was very evident congestion, shown especially well by Muir's method. The capillaries and small vessels seemed more numerous than normal, because they were rendered visible by being crowded mth red blood-corpuscles. At several places there were collections of cor- puscles, pointing to small extravasations of blood. These changes were present in the grey matter of the cord, medulla, and cerebral cortex. The appearance at once suggested that more or less permanent damage would have resulted had the animal lived. It has been observed in cases of tutu poisoning that sometimes the victim does not completely recover, a per- manent mental alienation remaining as an after-effect. Lauder Lindsay (3). in one case of poisoning he records, in which con- vulsions were a prominent symptom, notes that the subject never com- pletely recovered, " there remaining to this day a peculiar form of nervous irritability not observable prior to this toot-poisoning." The present writer has knowledge of another case, although, unfortunately, no authentic details are available, where two children were poisoned by tutu. They were both very seriously ill, and one died. The other recovered, but incom- pletely, mental enfeeblement and a squint remaining as after-effects. Sequelee of these kinds may possibly be explained as resulting from per- manent damage done to the nervous tissue by the extreme congestion and the small haemorrhages which occur in the cerebral cortex as well as through- out the whole grey matter of the central nervoiis system. Sympathetic Nervous System. — This was not speciallv examined b} ex- perimental methods, but that the nerve-cells here were also affected was shown by the viscid character of the saliva secreted by cats, by the dilata- tion of the pupil that occurred during convulsions, and by the erection of the hairs of the tail. In short, it is probable that tutin affects every kind of nerve-cell ; the fact that the medulla is seen to be specially affected being due to the sen- sitiveness of the cells in that region. Effect on the Pupil and Conjunctiva. — When dropped into the eye of a rabbit, tutin solutions cause no local irritation and no change in the size of the pupil (Exps. 160, 161). The same holds good for the cat (Exp. 162) and for the excised eye of the frog (Exp. 163). During convulsions in the cat and in pigeons dilatation is well marked. The action of coriamyrtin was studied in the same way. because it is said by Riban (15) to cause contraction of the pupil in rabbits when applied locally. It was found to cause contraction in the excised eye-ball of the frog, but the results of applying it to the eye of a rabbit and of a cat were negative (Exps. 164, 165). (f/.) Action of Tutin on General Nutrition. It is not an uncommon opinion among farmers that animals that eat the plant in moderation thrive well on land where tutu abounds. To test whether tutin had any injurious influence on general nutrition, a young FiTCHETT. — Physiological Action of Tutin. 327 rabbit (Exp. 166) was given small doses of tutin by the mouth every third or fourth day for nearly two months, the dose being gradually increased up to 7 mlgm. per kilo (6 mlgm. per kilo is a fatal dose by the mouth in rabbits). During this time the animal grew and developed normally, and it increased in weight from 777 grams to 1,154 grams. This shows that tutin does not retard growth. Another experiment was made on a guinea-pig (Exp. 167), the animal being treated like the rabbit. A second guinea-pig, as a control, was kept in the same hutch, and abundance of food was supplied. In thirteen days the animal subjected to the influence of tutin gained 16 grams, and the control in the same time gained 38 grams. The animals, however, were not of the same age ; the control, being younger, apparently gained more. From these data it looks as if tutin had no injurious influence on general metabolism (c/. Exp. 15, on a pigeon). 15. Fate of Tutin in the Body. It is impossible to trace in the body the fate of a substance which, like tutin, contains only C, H. and 0 ; but that the tutin is not rapidly destroyed or eliminated was shown by the following experiment (Exp. 13) : A guinea- pig was given by mouth on alternate days a dose of tutin which was near the minimum lethal dose ; thus, 1-5 mlgm. per kilo was given on the 17th, on the 19th. and on the 22nd February. No symptoms appeared, so the animal was able either to oxidize or to excrete this amount (1*5 mlgm. per kilo) in two days. On the 24th it received 2 mlgm. per kilo, and a similar dose w^as given on the 26th. On the 27th it was found dead. From this it appears that a guinea-pig is unable to dispose of 2 mlgm. per kilo within two days. Enough tutin must have been still present in the body on the afternoon of the 26th, when the second dose of 2 mlgm. per kilo was given, to raise the total amount present to the lethal dose. 16. Immunity or Tolerance. Several experiments were made with the object of determining whether tolerance of the effects of the poison can be estabUshed. A pigeon (Exp. 15) that had been subjected to gradually increasing doses by mouth over a period of ten days withstood 16 mlgm. per kilo. The minimum lethal dose in pigeons by oral administration is about 10"25 mlgm. per kilo. A second pigeon (Exp. 17), treated in the same way for over three weeks, succumbed to 12 mlgm. per kilo. A guinea-pig (Exp. 167), which was being treated in the same way, and had received several small doses, was killed by a dose of 7*5 mlgm. per kilo given by mistake, so that no great degree of tolerance had been estabUshed. A rabbit, already referred to above when considering the effects on general metabolism, received small doses, gradually increasing to 7 mlgm. per kilo, over a period of two months. A dose of 8 mlgm. per kilo then caused severe symptoms ; so that it would appear that a slight degree of tolerance had developed, for the lethal dose, by oral administration, in rabbits is about 7 mlgm. per kilo. Five days later this rabbit succumbed to a dose of 11 '6 mlgm. per kilo per os. The general conclusion reached was that tolerance can be established only in a very slight degree, if at all. 328 Transactions. 17. Pharmacological Eelationship of Tutin. Sclimiedeberg (30) placed coriamyrtin in the picrotoxin group of nerve and musc-le poisons. This group is closely allied to the camphor and digitalin groups, which include a number of the strongest non-nitrogenous poisons found in the vegetable kingdom. Other members of the group are circutoxin, a resinous substance derived from the water-hemlock ; oenan- thotoxin, from the Avater-dropwort ; digitaliresin and toxiresin, decom- position products of digitalin and digitalein respectively ; and oleandresin, from oleandrin. These substances, by their action on the medulla ob- longata, all cause general and respiratory convulsions, slowing of the pulse^ and a rise in blood-pressure. Tutin, as has been shown, possesses these actions common to the group. Some experiments were made to determine its toxic power as compared with picrotoxin and coriamyrtin (a very small quantity of the latter — 11 mlgm. — dissolved in absolute alcohol was kindly supplied by Mr. Aston, of the Agricultural Department of the New Zealand Government ; he. in turn, had obtained it from its discoverer, Monsieur Riban). Ttitin compared with Picrotoxin. — In the experiments on fishes already cited it was found that picrotoxin was more lethal than tutin when equal percentages of the two were used, and in equimolecular solutions it proved much more lethal. In mammals, on the other hand, tutin was found to be more fatal than picrotoxin. In Exp. 4 a cat received 0-375 mlgm. per kilo of tutin ; it developed severe symptoms, but recovered. Two days later it received exactly the same weight of picrotoxin (Exp. 168) without the development of any symptoms. The solution of picrotoxin used had been made seven months previously, and, lest it had deteriorated, a fresh solution was made and the same dose repeated five days later (Ex. 169) ; beyond defsecation and occasional swallowing-movements, no symptoms appeared. It was therefore concluded that tutin was more poisonous to mammals than picrotoxin. Following the procedure adopted in the case of fishes, the two were then compared in equimolecular strengths, and 883 0*375 X — mlgm. per kilo given hypodermicallv to the same cat (Exp. 170). 336 It developed twitching, vomiting, and other symptoms resembling those seen with tutin. Only one general convulsion occurred, however, whereas the dose of tutin had caused very numerous convulsions. It recovered in a shorter time, and the whole effect was much less severe ; so that, in con- tradistinction to fishes, mammals may be said to be more susceptible to poisoning by tutin than by picrotoxin. Tutin and Coriamyrtin. — The quantity of coriamyrtin mentioned above was insufficient for an extended series of experiments, and only one cat was subjected to its influence (Exp. 171). The symptoms were very similar to those of tutin poisoning ; twitching and convulsions were very marked. In the convulsions the tonic spasms were not so prolonged as in the case of tutin, the clonic element being more in evidence ; emprosthotonos appeared instead of the opisthotonos, which is so invariable a feature of tutin convulsions. Salivation, vomiting, respiration, erection of hairs of tail, and dilatation of the pupil were all present, as in turin poisoning. A strict comparison of its toxic power can hardly be drawn from one case ; but if the time taken to kill be proportional to the toxic power, tutin is the more lethal of the two, for 3 mlgm. per kilo of tutin killed a cat (Exp. 1) in thirty-one minutes, while this cat with the same dose of coriamyrtin died in forty-two minutes. FiTCHETT. — Physiological Action of Tutin. 329 (Exp. 172.) Twelve mlgm. per kilo proved fatal to a frog. It displayed tlie symptoms seen in tutin poisoning. The time of death could not be noted, so no strict comparison can be made with tutin. The minimum lethal ■dose of tutin in frogs is between 10 and 11 mlgm. On the whole, the impression left on one's mind is that there is com- paratively little difference in the toxic power of the two substances ; but the mental effects seemed more marked in the case of the cat poisoned by tutin. 18. Action of Remedies. Although not strictly within the scope of the title of this paper, notes of some experiments made to show the influence of remedial measures will be included here. These experiments were made from time to time while the physiological action of tutin was being examined, and before the experi- ments on the action of alkalis on tutin had been undertaken. They are necessarily, therefore, incomplete ; but some points have been investigated -and some observations made which it is hoped may prove of value in the treatment of cases of poisoning. In tutu poisoning various remedies have been suggested from time to time, and the rationale of some of these is difficult to understand. With shepherds, bleeding is a favourite method of treatment. It is usually done by slashing the ears or tail, or by incising the roof of the mouth. It is said to be of special advantage in young sheep, but in older sheep it is regarded by some as being dangerous, and as tending rather to hasten the end than to promote recovery. Carbonate of ammonia is also used, a lump about the size of a walnut being dissolved in water and poured down the animal's throat. In 1870 Hughes advocated the use of lime as an antidote. He was led to do this from the observation he had made that lime destroyed the activity of the poison. Cases in human beings have been treated with lime, and, it is said, successfully. The Maoris depended largely upon partial asphyxiation as a means of treatment. This was effected either by holding the patient under water till he was nearly drowned, and repeating the immersion as soon as he showed signs of returning life, or by suspending him head downwards over the smoke of a fire. Another method (31) was to bury the patient in the ground up to the neck, apparently with the object of restraining the con- vulsive movements. Professor Marshall (32), in a report made to the Agricultural Depart- ment of the New Zealand Government, recommends bleeding and the intravenous injection of chloral-hydrate. In connection with the use of chloral-hydrate it may be noted that Crichton Brown (34) states that he was able, by the administration of chloral-hydrate, to prevent death in a rabbit which had received five times the minimum lethal dose of picrotoxin. It will be noticed that in a rabbit (Exp. 17-1) which received a lethal dose (3 mlgm. per kilo hypodermically) death was prevented by 0-6 gram of chloral-hydrate. It should be stated that the chloral was given first by the rectum, and the tutin administered hypodermically as soon as the anaesthetic effect of the chloral was established, so that every chance was given to the action of the chloral. In two rabbits where 4 mlgm. of tutin per kilo was given (Exps. 173, 175) death occurred. The one received 1 gram of chloral per rectum in one dose, and the tutin hypodermically immediately afterwards ; it died in six hours, in tutin convulsions. The 330 Transactions. other received 0-6 gram chloral per rectum, and while asleep, ten minutes later, the tutin was given hypodermically ; symptoms of tutin poisoning came on in less than two hours, and continued for an hour and a half ; as the animal seemed likely to succumb, a further dose of 0-6 gram chloral was given, and in about a quarter of an hour the symptoms subsided, and the animal apparently recovered ; next day it was suffering from diarrhoea, and the following day was found dead ; possibly it died more from the after-effects of the chloral than from tutin, and it looked as if a little care- ful nursing would have led to its recovery. The results of some experiments made with chloral as a remedy in tutin poisoning are given in Table IX. Table IX. Action of Chloral in antagonising Tutin. Dose of Exp. No. Animal. Tutin in Mlgm. per Kilo. Usual Result. Remedy used. Result. Remarks. Chloral. 167 Guinea-pig 7-5 .. Death within 1 hour 0-5 grm. .. Died in 45 hours Died apparently from chloral. 173 Rabbit . . 4 .. Death within 2^ hours 0-6 grm., fol- io wed by a second dose of 0 6 grm. Died between 24 and 48 hours. 174 // • • 3 .. Death within 3 hours 0-6 grm. .. Recovered completely. 175 ff • • 4 .. Death within 2^ hours 1 grm. given simultane- ously Died in 6 hours Tutin symptoms. 177 Prog 12 .. Death 0-012 grm. Died. 178 // 11 .. // • • ^^ /' 179 V • . 12 .. „ // „ 176 '/ • • No tutin " Lived. was given A guinea-pig (Exp. 167) which had received 7-5 mlgm. tutin per kilo by mistake, and was then given chloral per rectum, died in a somewhat similar manner. It recovered fully from the tutin convulsions, but became paralysed in its hind quarters, and died on the second day after the tutin It also had diarrhoea. Frogs (Exps. 177, 178, 179) which were given just over the lethal dose of tutin (11 and 12 mlgm. per kilo) were not saved by chloral in moderate doses given hypodermically at the same time. Control Exp. 176. On the whole, the use of chloral seems to be justified, and in cases of poisoning in man, where the symptoms can be more accurately observed and interpreted, and dangers more easily circumvented, it should prove of great value. The beneficent action of tutin on the heart would allow of the use of larger doses of chloral than are usually employed. Paraldehyde and Chloroform. — In the experiments on blood-pressure, where the animal was under a large dose (1*2 to 1*5 c.c.) of paraldehyde, convulsions nevertheless appeared, and the mode of death was that of tutin poisoning. From such a dose of paraldehyde a rabbit may recover (Exp. 181), but the dose is a massive one, and is apparently unable to prevent the development of tutin symptoms. In these experiments, when it was FiTCHETT. — Phijsiological Action of Tutin. 331 desired to keep the animal quiet it was found that chloroform-inhalation was sufficient for this purpose. The amount required seemed to be great, but there was no available means of accurately gauging the quantity. It was noted in some cases that the convulsions did not cease until the blood- pressure began to fall, and this, taken in conjunction with the fact that reflex excitability of the nervous system is raised, and that tutin therefore increases the effect of any reflex cardiac inhibition which may be present, points to the need of caution in its administration in cases of tutin poisoning ; in fact, in one case of tutin poisoning in a rabbit, when urethane and sodium-carbonate had had no effect in easing the symptoms {Exp. 180), the administration of chloroform caused sudden cessation of the breathing, which could not be restored, although the heart continued beating and artificial respiration was carried out. Urethane, tried in one case (Exp. 180) just mentioned, was ineffectual. A dose of 1*5 grams was given to a rabbit weighing 1'4 kilograms, and 4 mlgm. tutin was then administered. The ordinary tutin symptoms developed, though a little later than is usual with so large a dose. Morphine. — | grain injected intravenously at (25) on tracing of Exp. 148 had no effect on the convulsions of a rabbit under paraldehyde. A severe convulsion folloAved very shortly after the injection. Atropine. — J^ grain given in the same way at (23) on tracing of Exp. 148 had no effect. Hyoscine hydrohromate (Exp. 182) was found to be curiously inactive as regards rabbits, y^^ grain in all was given to a rabbit weighing 1*5 kilo- grams, but apparently it had no effect at all, so its influence on tutin symptoms can be disregarded. Bleeding is frequently used in cases of tutin poisoning, and is said to do good ; but it is very difficult to judge of the value of the evidence. In the experiments on blood-pressure the animals were frequently bled to death slowly, but no cessation of the tutin spasms was observed in any case. Restraint of the movements was tried in one experiment on a pigeon, but without influencing the result in any way. Suspension of a rabbit under the influence of tutin by the ears or hind legs had no effect on the spasms. Partial asphyxiation, by blocking the nostrils with a damp cloth — (26) on tracing of Exp. 148 — had no effect on the convulsions ; but a stream of CO 2 directed against the nostrils seemed to render the breathing more regular (27). Alkalis (Lime, &c.). — Hughes's discovery of the action of lime on tutin, although generally discredited at the time and since, may possibly be utilised to some extent in a modified form. Alkalis in general have been shown in the foregoing pages to have a very distinct action on the toxicity of tutin : thus 0*2 per cent. NaOH in five minutes at 37° to 40° C. completely destroyed the toxicity of a 0"5-per-cent. solution of tutin, and possibly the same result would follow in a shorter time and with a weaker alkali. Since this is so, the treatment of stock poisoned by the tutu plant may be greatly improved. It is impossible to fully wash out the stomach in herbi- vora, so there is no way of getting rid of the leaves, &c., swallowed by the animal ; but the introduction of a quantity of weak sodium-hydrate, or lime-water, or a watery suspension of magnesia simply poured down the throat, or, better, introduced by a stomach-tube, would lead to the neutrali- sation of the tutin present in the stomach, and so give the animal a better -chance of recovery. The accumulation of gas would at the same time be 332 Transactions. diminislied by the^absorption of the CO 2, wliich no doubt forms part of the mixture of gases present, so the distension that so frequently occurs in these cases would be diminished. The comatose condition which forms part of the symptoms of tutin poisoning suggested the possibility of some form of acid poisoning being present, and, if this be so, the injection of alkalis should prove of benefit. Sodium-carbonate was tried intravenously in one of the blood-pressure experiments, but no apparent effect was observed. In another case sodium- carbonate was injected into the rectum of a rabbit that seemed likely to die- of tutin poisoning, but here also it was ineffective. So that for the present one can only say that alkali would render unabsorbed tutin non-toxic. 19. General Summary. 1. Investigations made on the action of the pure principle tutin (C17H20O7) confirmed the results of previous observers that it is in itself sufiicient to account for the main bulk, if not the whole, of the symptoms of poisoning by the tutu plant. 2. These symptoms, as they occur in cats, have been fully described, and the differences which appear in other animals noted. 3. Tutin, or its metabolic products, acts mainly on nerve-cells, producing first increased excitability and then exhaustion. It specially affects the cells of the respiratory centre, causing increased rate and depth of respiration. 4. Death may occur during the phase of increased excitability (asphyxia during convulsions) or in the phase of exhaustion. Various reflex acts — vomiting, defalcation, micturition^ — may occur during the stage of increased excitability. A comatose condition, possibly due to exhaustion of the cells of the cerebral cortex, is a marked feature in proportion to the strength of the dose. It deepens as death approaches. Small haemorrhages 'into and congestion of the grey matter of the brain and cord are marked features in fatal cases. The Nissl granules seem unchanged when death occurs in a short time. 5. In strong solutions tutin has a slight deleterious action on tissues less highly specialised than nerve tissue — e.g., ciUated epithelium and muscle. It retards the growth of some forms of bacteria, and injuriously affects para- moecia and other low forms of life in relatively strong solutions. 6. The symptoms of poisoning by tutin are in a general way similar in widely different forms of life (flies, pigeons, cats, (fee), and can all be referred to an action on nerve-cells. 7. The minimum lethal dose in milHgrams per kilo of body-weight for different classes of animals is as follows : — Hypodermically. Per Os. [mmersion in. Mlgm. • Mlgm. Mlgm. Cats . About 0-75 , , Eabbits „ 2-5 About 6 Guinea-pigs . „ 2 • « Birds Less than 5 Between 10 and 10-25 Lizards . Between 3 and 4 • • Frogs 10 and 10-25 • • Fishes • • • *• • About 50 8. The effects on the various systems can all be referred to the influence- on their nerve mechanisms — e.g. : Alimentary system, salivation, vomiting (on hypodermic injection). The circulatory system is not injuriously afl'ectedi FiTCHETT. — Physiological Action of Tutin. 333 by tutin. Cardiac inhibition does not occur, and the heart beats forcibly up to the time of death. Respiration is quickened and deepened. The pupil is not aft'ected by local appUcation, but dilates during the tutin fit. General metabolism is not affected. 9. From experiments on birds and rabbits, some slight degree of tolerance seems to be acquired. The natural relative immunity of birds is discussed. 10. Accumulation of the drug, or of its effects, may occur. Thus a guinea- pig was found to be unable to dispose of 2 mlgm. per kilo per os adminis- tered every second day. 11. The toxic action of tutin was compared with that of other members of the picrotoxin group. It was found to be more toxic than the sample of picrotoxin employed. The action of coriamyrtin was found to be very similar to that of tutin. 12. Attempts were made to antagonize the action of tutin with chloral- hydrate and other drugs, with a slight degree of success. Attention is drawn to the powerful action of weak alkalis on tutin. The toxic power of tutin is completely destroyed by 0"2 per cent, sodium- hvdrate acting upon it for five minutes at 37° C, and possibly the action of weaker alkalis — e.g., lime and magnesia — would be equally destructive. The suggestion is made that weak alkali should be used to destroy the tutin in the stomach in the case of stock poisoned by eating the tutu plant. I may state here that the bulk of the work was done in the physiological laboratory of the Otago University, and I gladly take the opportunity of acknowledging my great indebtedness to Professor Malcolm, both for this privilege and for the essential aid he has afforded me by advice and criticism. I wish also to acknowledge my obhgation to Mr. Aston for supplies of tutin and coriamyrtin, and for several references ; to Dr. Hocken, for the use of his invaluable library ; to Professor Benham, for the identification of specimens ; to Mr. Deans, of the Acclimatisation Society, for suppHes of trout-fry ; and to Nurse Stronach, of the Infectious Diseases Hospital, Lake Logan, for supplies of minnows. PROTOCOLS. Exp. 1. P.M. Cat (female). Weight, 3-28 kilograms. 5.25. Gave 33-4 minims of a 0-5-per-cent. solution of tutin in 0-75 per cent, saline (3 mlgm. per kilo body-weight), under skin of back. 5.29. Respiration rapid (48 to the quarter-minute) ; hypersalivation ; keeps mouth agape ; panting vigorously. 5.32. Lying on bottom of cage panting, respirations audible ; mouth open ; thick ropy saliva pouring from mouth ; whole body shaking with respiratory effort ; j)upils moderate. 5.35. Becoming restless ; walks cautiously about cage. 5.35^^. iSuddenly seized wdth violent convulsion ; tonic spasm affecting all muscles, lastmg 30 seconds, succeeded by clonic spasms ; pupils widely dilated ; defaecation ; micturition ; nose cyanosed ; unconscious, conjunctival and ear reflex absent. 5.44. Almost constant convulsion since last note ; now becoming exhausted ; re- spiration slow, irregular, spasmodic ; pupils dilate during convulsions, con- tract in intervals. 5.45. Respiration infrequent and jerky ; fits in abeyance ; lies full stretched on side ; twitching of individual muscles. 5.47. Fit after three mimites' interval ; tonic spasm not succeeded by clonic. 5.49. Occasional gasping respirations ; writhing- movements of body. 5.51. Clonic spasm, with a few involuntary cries. 5.53^. Clonic spasm. 334 Transactions. P.M. 5.54. Mistaken for dead, but still respiring feebly, and at rare intervals. 5.56. Respiration ceased ; heart inaudible with stethoscope ; pupils dilated ; dead. Temperature in rectum, 102° Fahr. F.M. — Rigor mortis extremely well marked ; no sign of fluid at point of injec- tion ; blood very dark and fluid. Abdomen : Right horn of uterus contains one foetus nearly full size, which looks as if it had died in spasm ; one hind leg twisted over the other ; right paw behind right ear ; claws extruded. Gall-bladder contained bile. No obvious abnormalities. Thorax : Great veins and right side of heart distended \vith blood : left side con- tained some dark blood ; lungs showed small hemorrhages, as also did the thymus. Brain and cord : The membranes seemed somewhat injected ; grey matter of cord appeared distinctly pinkish to the naked eye. Microscopic : The cord and medulla were hardened in 8 per cent, formol, and carried through into paraffin, and sections cut. The sections were stained by Nissl's method with toluidin blue. On examination the granules were found to be present and normal in appearance. A marked feature was the congestion of the grey matter. Capillaries can be seen close up to the nerve-cells c^uite full of corpuscles. At other places the collections of corpuscles suggest that minute hsemorrhages had occurred. The cord, medulla, and cerebrum show these appearances, but the congestion of the medulla is the most marked. Exp. 2. P M_ Cat (female). Weight, 3-50 kilograms. 5.0. Gave 23-8 minims of a 0-5-per-cent. solution of tutin in 0-75 per cent, saline (2 mlgm. per kilo body-weight), under skin of back. 5.1. Gave a deep sigh. 5.6. Lying in a normal attitude on bottom of cage ; looks sleepy ; respirations, 21 to the half-minute ; pupils moderate. 5.10. Still lying down; looks sleepy, and is tremulous. 5.14. Opening mouth wide; cries loudly; respirations panting, 56 to the quarter- minute ; has got up ; salivating. 5.19. Lying down ; mouth wide open ; panting; salivatmg. 5.21. Slight twitching of muscles of face ; cries at intervals ; pupils moderate. 5.22. Twitching of head. 5.23. Twitching of head, followed by loiid cries, as if alarmed, without knowing at what. 5.24. Deftecation, large quantity of solid faeces ; twitching of head. 5.25. More marked twitching of head, extending to shoulders and fore paws ; twitch- ing is now almost without interval, and rapidlj^ becoming more severe ; pupils dilated, but not full ; respirations irregular, suggestive of Cheyne-Stokes. 5.29. General con\nilsion, pupils widely dilated, tonic stage lasting 30 seconds. 5.40. Has continued lying on side since first convulsion ; is imable to see ; conjunctival reflex sluggish ; convulsions have continued with intervals of only two or three seconds since last note ; seems unconscious ; pupils contract in inter- vals. 5.45. Becoming exhausted, convulsions becoming feebler and rarer ; respirations slow, irregular, gasping. 5.51. With a fuaal spasm and choking invokmtary cry, died. Exp. 3. P.M. ("at (female). Weight, 2-394 kilograms. 2.32. Gave 5-9 minims of a 0-5-per-cent. solution tutin in normal saline (0-75 mlgm. per kilo body-weight), under skin of back. 2.55. Sitting purring ; pupils moderate ; keeps swallowing, as if swallowing saliva ; respiration, 48 per minute ; '' miauing " plaintively ; made water ; defsecatecl (diarrhosa and flatulence), did not finish act, but walked away with discharge still pouring from anus ; looks sick. 3.0. Keeps mouth open ; pantiiig respiration ; salivation ; vomited, vomit shot out without retching. 3.3. Straining at stool and " miauing " ; looks ill and miserable, and disinterested in its suiToimdings. 3.5. Begun to purr ; has laid down curled up, as if to sleep. Z.l. Has got up ; sitting on haunches purring ; twitching of muscles of face ; still swallowing saliva. FiTCHETT.^ — Physiological Action of Tutin. S35 P.M. 3.9. Lies down again ; twitching of face getting more marked, and extending to shonlders ; each attack of twitching followed by loud " miauing," and, as it gets more marked, by growling ; pupils dilate with each attack. 3.13. General convulsion lasting one minute ; saliva pouring from mouth ; loud voluntary crying after convulsion ; conjvmctival reflex present, pupils widely dilated ; can see ; respiration laboured ; keeps lying on side. 3.19. Stands up and looks round cage ; breathing easier ; pupils not so large. 3.21. Walked to another corner of the cage, and sat down ; looks frightened and uneasy ; has been no twitching for some time ; breathing quite easy, and only a little hurried ; salivation seems to have ceased ; constant loud crj- ing ; pupils moderate. 3.32. Has been quiet since last note ; looks as if it might recover. 3.34. Now crying loudly, and showing slight twitching of head. 3.35. Twitching getting more severe; loud prolonged plaintive cries; sitting up on haunches, looking round. 3.36. Walks across cage with cautious unsteady steps. 3.40. Twitching getting much more marked and more extensive, as if another general convulsion were about to occur ; loud crying ; whole body tremulous ; re- spiration hurried and exaggerated, panting with mouth open ; put its head into the drinking-bowl, but did not lap ; is restless. 3.42. Most severe general convulsion, lasting 4^ minutes, then a long-drawn inspira- tion. 3.50. Convulsions have continued almost without interval, but now becoming less severe ; much frothing at mouth ; gave a cry in an interval. 3.51. Choky cries occur in the intervals between the conv\dsions ; respirations ir- regular and gasping. 3.55. A longer interval, with loud crying ; respirations in the interval, 14 to the quarter- minute. 4.2. Has been in almost continuous convulsive movement, with comparatively quiescent intervals of only a few seconds, since 3.43 ; in a longer interval than usual attempted to rise, but knocked down again by a convulsion. 4.4. Seizures shorter ; intervals longer, about 20 seconds to 5 seconds. 4.6. After a more severe convulsion than usual respirations are now very slow, irregular, and gasping. 4.9. No convulsions since last note ; respirations more rapid ; running or swimming movement of limbs ; attempts to rise, but knocked down by a convulsion. 4.15. Gave a voluntary cry. 4.20. Continues in constant more or less voluntary movement. Has been no. con- vulsive seizure since 4.9 till now. 4.21. No respiratory or other movement since last fit. Is dead. Exp. 4. P.M. Cat. Weight, 2-686 kilograms. 3.46. 3-4 minims of a 0-5-per-cent. solution tutin (0-375 mlgm. per kilo), injected under skin of back. 3.58. Defsecated, hard motion, covered it up ; begimiing to swallow ; does not look so bright as it did ; is quiet ; no change in pupils ; breathing more marked ; beginning to look sleejiy. 4.2. Swallo\^ing repeatedly ; looks very sleepJ^ 4.10. Opening mouth and panting; vomited freely and forcibly, a large quantity of stomach-contents being ejected ; micturated. 4.20. Twitching of eyelids and ears. 4.30. Has shown twitching of face, head, and neck at short intervals ; " miaus " occasionally. 4.40. Twitching becoming exaggerated, involving shoulders, fore limbs, and back. 4.43. General convulsions, severe. 4.47. Gets up after convulsive movements have gradually subsided. 4.50. Looks very ill ; sitting on jiaunches ; tremulous breathing exaggerated : answers when spoken to ; twitching beginmng again ; salivating. 4.56. Respirations 48 to the quarter-minute ; lying quiet. 5.15. Twitcliing gettmg more marked; cries after each attack. 5.19. Still twitching. 5.21. Twitching involving more muscles. 5.30. Twitching getting very marked ; at each attack animal almost springs into the air ; loud crying ; breathing very exaggerated ; opens mouth occasionally, and pants for a few seconds. 336 Transactions. P.M. 5.34. General convulsion. 5.36. Up again ; takes no notice when called ; lying panting, with mouth open. 6.0. Has continued twitching every few minutes since last note ; now getting verj- marked. 6.5. Severe general convulsion, lasting 1 minute. 6.6. Rose again ; pupils widely dilated when convulsed, diminish in size in the intervals. 7.15. The cat has not been seen since last note till now ; it is sitting on its haunches, tremulous, " miaus " when approached. 7.40. Same. 8.30. Sitting quietly ; easily startled. 9.30. Apparently recovered ; no symptoms noticed. Next day, 9 a.m. Seems quite well. Exp. 5. A.M. Rabbit. Weight, 0'729 kilograms. 10.43. Gave 5 minims of a 0'5-per-cent. solution tutin (2 ralgm. per kilo), hypodermically. 11.15. No apparerrt change. 12.0. Standing in middle of cage ; does not appear at ease. P.M. 12.10. Animal near front of cage ; semi-dazed ; starts when disturbed. 1.10. Much the same, quiet and dazed-looking. 2.10. Seems normal. 3.0. Gave some food. 5.0. Food untouched, but no obvious symptoms. Next day. Quite well. Exp. 6. A_]VI, Rabbit. Weight, 962 grams. 9.56. Gave 8'2 minims of a 0"5-per-cent. solution of tutin in normal saline (2"5 nilgm. per kilo). 11.0. Noticed to be in convulsions ; last seen about 10.30, was then quiescent. 11.10. Sitting \ip ; dazed-looking. 11.11. Another convulsion began, fell on side, clonic spasms; head bent back, ears twitching. 11.17. Still in convulsions. 11.32. Con^Tdsions. 11.52. Lying on side, head bent back ; running-movements. 12.22. Died. Exp. 7. A jj Rabbit. Weight, 788 grams. 10.4. Gave 8 minims of a 0'5-per-cent. solution tutin (3 mlgm. per kilo). 10.50. Slow, deliberate winking. 10.55. Lying on right side ; breathing laboured. 11.4. In clonic convulsions, with movements of jaw and exposure of teeth. 11.15. Still in almost constant convulsion. 11.20. Dead. Exp. 8. p_jj_ Rabbit. Weight, 1-507 kilograms. 5.12. Gave 38-4 minims of a 0-5-per-cent. solution tutin (7-5 mlgm. per kilo), per os. Was not watched constantly, but at — 5.45. Was found to show great rapidity of respirations ; alteration in gait — e.g., moved forward with difficulty, with body elongated, and abdomen trailing on floor ; then lay on abdomen, with hind legs projecting behind, twitching of eyes and ears. 6.5. Was found in severe general convulsions, head retracted, tonic spasms well marked ; running-movement of legs between fits ; was held up by the ears, but this did not influence the convulsions, and no influence when suspended by hind legs. 6.25. Constant movements, either convulsive seizures in which the head is always firmly retracted, or running-movements ; is quite unconscious ; eyes wide open, and, as it lies on its side, rubs the open lower eye into the sawdust during seizures. 6.45. Dead. FiTCHETT. — Physiological Action of Tutin. 337 Has evidently died from Exp. 9. p jyj Rabbit. Weight, 1-16 kilograms. 6.0. Gave 6 mlgm. per kilo, by mouth. 7.25. Respirations seem more rapid than usual. Next day, 9 a.m. Dead. Rigid, in oposthotonic posture, tutin. Exp. 10. P ji Rabbit. Weight, 1-069 kilograms. 3.6. Gave 17-5 minims of a O'o-per-cent. solution tutin (5 mlgm. per kilo), per os. 3.45. Has displayed no symptoms. Next day. Quite normal. . Exps. 11, 12. Two guinea-pigs, A and B. Weight of A, 624 grams (Exp. 11) ; weight of B, 684 grams (Exp. 12). To A, gave 2 mlgm. per kilo body-weight ; to B, gave 3 mlgm. per kilo body-weight. P.M. 3.20. Gave to A 4-2 minims of a 0-5-per-cent. solution tutin, under skin of back. 3.40. Gave to B 7 minims of a 0-5-per-cent. solution tutin, under skin of back. Both pigs were placed in the same cage, but B attacked A so viciously that it was necessary to separate them. 3.50. A seems tremulous. 3.55. A obviously affected, twitching and starting. 4.0. B affected in the same way. 4.5. Both in violent and continuous convulsions. 4.10. B removed from cage, and 17 minims of a 0-05-per-cent. solution of chloral- hydrate injected (equal to 0-011 grams per kilo). 4.15. B dead ; killed in 35 minutes. Mouth and nostrils found blocked with sawdust from the bottom of the cage. 4.15. A still in constant convulsions ; becoming feebler. 4.30. A dead ; has continued in constant movement since convulsions appeared ; killed in 70 minutes. Result. — A killed in 70 minutes by 2 mlgm. per kilo ; B in 35 minutes by 3 mlgm. per kilo. Exp. 13. Guinea-pig. Weight, 751 grams. Feb. 13. Gave 4 minims of 0-5-per-cent. solution tutin (1-5 mlgm. per kilo), per os. Weight, 768 grams. Gave 4 minims of 0-5-per-cent. solution, per os. 17. 19 20 22 24 824 grams. Gave 5-2 minims of a 0-5-per-cent. solution (2 ralgm. per Gave 4 minims of 0-5-per-cent. solution, per os. Has displayed no symptoms. Weight, 809 grams. Gave 4 minims of 0-5-per-cent. solution, per os. ,, 823 grams. Gave 5-5 minims of 0-5-per-cent. solution tutin (2 mlgm. per kilo), per os. No symptoms. Weight, 767 grams. kilo), per os. Found dead in the morning. Result. — Was able to eliminate 1-5 mlgm. per kilo given every second day, but unable to eliminate 2 mlgm. per kilo in two days. In this experiment the influence of the prolonged administration of tutin on the weight of the animal was tested by keeping a second guinea-pig under similar conditions as a control. The weights of the two animals as taken during the course of the experi- ment were as follows : — A 26. 27. Feb. 13 17 19 22 24 26 (Control). Grains. 595 589 607 627 633 B. Grams. 751 768 824 809 823 767 Result. — Control gained 38 grams ; tutin animal gained 16 grams. 338 ' Transactions. Exp. 14. Giiinea-pig. Weight, 1 lb. Fed up to this morning. 10.53. C4ave 5 minims of 0-5-per-cent. tutin ; injected into mouth, and fluid was readily- swallowed. 10.55. Animal seems quite as usual, though easily frightened. 11.0. Same. 11.10. Still same ; trying to chew straw in cage. 11.20. Gave it some wet green grass, which it ate greedily. 11.45. Quiescent ; has not eaten much grass ; apparently normal. P.M. 12.5. Seems still quite normal. Gave other 5 minims in same way (about 3-5 mlgm. per kilo). 12.20. Stretching-movements (? normal). 12.30. Normal. 12.33. Sudden onset of symptoms ; convulsive movements ; stood on liind legs till fell over backwards ; rushed several times round cage ; then tonic spasm, lying on side ; respii'atory movement increased ; twitching of ears and fore part of body. Then became quiescent, lying still on right side. 12.40. Resumed usual sitting-position. 12.48. Still quiescent. 12.50. Moved slowly round several times against dii'cction of a clock. 1.3. Another fit began, with twitching of head backwards and upwards ; then running- movements of limbs. It ran to front of cage, got its nose into one of the meshes, and tried, as it were, to run forward rapidly ; then ran towards another corner, but fell on its side, and went into a clonic spasm, moving its fore and hind legs vigorously ; then came a more tonic spasm of whole body ; fine ti'emors ; swallowing and gasping movements ; mouth open. By 1.7 it became quiescent again. 1.10. Another fit; lying on side and working its fore and hind legs ; head bent back on body, but whole body not rigid. 1.15. Still same, but movements slower. 1.40. Same condition. 1.50. Movements continue practically without cessation. 1.55. Same. 2.0. Same, slight cries. 2.5. Same. 2.15. Movements less frequent. 2.17. Quiescent; dead. 2.30. Rigor mortis seems to be setting in already. 2.45. Rigor distinct. P.M. (3.30). — Rigor well marked ; abdomen opened ; some grass observed in stomach and intestines, but no great accumulation of gas. Exp. 15. Pigeon. Weight, 314 grams. Jan. 14. Gave 2 mlgm. tutin per kilo body- weight, per os. 15. No effect, so gave 4 mlgm. per kilo, per os. 18. No effect, so gave 6 mlgm. per kilo, per os. 19. Bird seemed dull and heavy for a few hours after the dose ; took no food, and moped in a comer, with feathers puffed out. Is quite well to-day. 20. Reweighed ; same weight. Gave 8 mlgm. per kilo, per os. 21. A repetition of symptoms noted pre-\'iously. Is quite well to-day, so gave 10 mlgm. per kilo, per os. 22. Same symptoms as before. Quite well to-day, so gave 12 mlgm. per kilo, per os. 23. Same symptoms as before. Quite well to-day, so gave 16 mlgm. per kilo, per os. 24. Same symptoms as before, but quite well to-day ; so at 12 noon gave 20 mlgm. per kilo, per os, on an empty crop. At 12.45 p.m. bird found lying on back in convulsions ; marked retraction of head, and constant movements of feet and flapping of wings. At 12.50 p.m. movements becoming feebler and slower. At 1 p.m. dead ; weight, 345 grams, an increase of 31 grams. P.M. — Crop noted to be empty ; nothing abnormal detected. Result. — 16 mlgm. per kilo non-lethal ; 20 mlgm. per kilo killed in one hour. FiTCHETT. — Physiological Action of Tutin. 339 Exp. 1(5. A.M. Pigeon. Weight, 319 grams. 10.6. Crave 18-3 minims of 0-5-per-cent. solution tutin in normal saline (17 mlgm. per kilo body-weight), per os. 10.8. First appearance of symptoms, tremulousness and jerking of head ; sudden slight expansive movements of the wings. 10.10. General con^n^lsions ; marked opisthotonus; bird turning over and over, head firmly retracted on back, wings widely extended, genei'al convulsive move- ments. 10.13. Has been no cessation, of convulsive movements since onset ; now becoming more feeble. 10.21. Movements very feeble ; bird apparently been unconscious since onset. 10.22. All movements ceased. P.M. — Crop opened ; found empty, except for a small amount of grumous fluid con- taining small yellow particles. Sour smell, and distinct acid reaction. No abnormality observed. Result. — Death in 16 minutes from 17 mlgm. per kilo. Exp. 17. Pigeon. JFeb. 7. At 6 p.m. gave 2 mlgm. of a 0-5-per-cent. solution tutin (about 1-5 mlgm. per kilo), per os. At 7.5 p.m., apparently normal. At 10.45 p.m., same. 8. Quite normal. Gave 3 mlgm. of a 0-5-per-cent. solution tutin (about 2 mlgm. per kilo), per os. 10. At 6 p.m. pigeon weighed 396 grams. Gave 5-3 minims of a 0-5-per-cent. solution tutin (4 mlgm. per kilo), per os. 11. Normal. 14. Weight, 408 grams. Gave 9-7 minims of a 0-5-per-cent. solution (9 mlgm. per kilo), per os. 15. Normal. 17. At 6-3 p.m. weighed 388 grams. Gave 11-8 minims of 0-5-per-cent. solution tutin (9 mlgm. per kilo), per os. 18. Normal. 19. Weight, 342 grams. Gave 10-8 minims of 0-5-per-cent. solution tutin (9-5 mlgm. per kilo), per os. 20. Normal. 24. Weight, 343 grams. Gave 11-6 minims of 0-5-per-cent. solution tutin (10 mlgm. per kilo), per os. 25. Normal. 26. At 6 p.m. weighed 370 grams. Gave 15-4 minims of a 0-5-per-cent. solution tutin (12 mlgm. per kilo), per os. At 6.20 p.m. squatting on floor of cage ; very tremulous about head and neck ; blinking repeatedly. ,, 27. Found dead in the morning. Result. — No tolerance developed. Death from a dose of 12 mlgm. per kilo. Exp. 18. Jan. 28. Pigeon. Weight, 357 grams. P.M. 5.45. Gave 18-2 minims of a 0-5-per-cent. solution tutin in normal saline (15 mlgm. per kilo body-weight), per os. 7.30. Beyond some dullness and. heaviness, no symptoms. Next day. Quite normal. Result. — Recovery from 15 mlgm. per kilo. Exp. 19. . P.M. Pigeon. Weight, 374 grams. 6.7. Intended to give 20-3 minims of a 0-5-per-cent. solution tutin (16 mlgm. per kilo body-weight), but a few drops were lost, so gave 5 minims more. 6.10. General convulsions; marked extension of wings arui bending- backwards of the body, so that the bird rests on its tail. 6.12. Lying on back, in constant convulsive movement. <3.16. Dead. P. 31. — Crop half-full. No abnormality detected. Result. — Death in 9 minutes from a dose of about 16 mlgm. per kilo. 340 Transactions. Exp. 20. P.ji. Pigeon. Weight, 319 grains. 5.6. C4ave 17-3 minims of a 0-5-per-cent. solution tutin (16mlgm. per kilo body- weight), per OS. 5.7. Appearance of symptoms. 5. 7 J. Clonic convulsions began. 5.11. Movements ceased ; pupils dilated ; dead. P.M. — Crop full of half-digested food. No abnormalities observed. Result. — Death in 5 minutes from a dose of 16 mlgm. per kilo. Exp. 21. P.M. Pigeon. Same as used in Exp. 14. Weight, 345 grams. 5.14. Gave 16-8 minims of a 0-5-per-cent. solution tutin (15 mlgm. per kilo body- weight), per OS. Had received no food since the day before. 5.20. Seems quite normal ; is preening its feathers. 5.21. Attempting to vomit. 5.22. Retching. 5.23. Retching. 5.24. Retching ; drowsy-looking ; tremulous about head. 5.24.^. Retching. 5.25. Squatted do\\^l on bottom of cage. 5.25.K Retching. 5.2(i. Very tremulous about head and neck; dazed and sleepy looking; retching every half-minute or so. 5.29. Twitching of muscles of neck ; head being drawn back with sharp jerks. 5.36. Slight convulsions affecting the fore part of the body ; wings rigidly extended, and marked clonic movements of tail and neck ; remains standing between the attacks ; blinks its eyes heavily, as though onlj' keeping awake with the greatest effort ; pupils contracted. 5.40. A more severe convulsion ; bird thrown over on to its back, but recovered its position again. 5.43. A most severe convulsion, bird thrown over backwards ; lies on back, with head bent back beneath body ; all muscles in continuous clonic spasm. 6.49. Convulsions have continued without intermission since last note ; movements now becoming feeble. 5.50. All movements ceased ; dead. P. 31. — Crop empty. No abnormality observed. Besvlt. — Ivilled in 35 minutes by a dose of 15 mlgm. per kilo, Exp. 22. P.M. Pigeon. Weight, 203 grams. 5.13. Gave 10-3 minims of a 0-5-per-cent. solution tutin (15 mlgm. per kilo), per os. 5.20. Lying on back, in continuous convulsive movement. 5.25. Gave 10 minims of a 1-in-l solution chloral-hydrate, equal to 0-6 gram chloral, per OS. 6.25. Dead. P.M. — Crop half-full. No abnormality observed. Result.- — Death in 72 minutes from 15 mlgm. per kilo. Life evidently prolonged by the chloral. Exp. 23. P.M. Pigeon (young). Weight, 375 grams. (Fed at 1 p.m.) 3.49. Gave 15-5 minims of 0-5-per-cent. solution tutin (13 mlgm. per kilo body-weight), per OS. 3.52. Slight attempts at vomiting. 4.0. Lying on back, in convulsions ; convulsive movements continued till death. 4-8. Death. Result. — Death in 19 minutes from 13 mlgm. per kilo. Exp. 24. P.M. Pigeon (young). Weight, 363 grams. 3.46. Gave 14-8 minims of 0-5-per-cent. solution tutin (12 mlgm. per kilo body-weight), per OS. 3.50. Vomiting repeatedly, bringing up quantities of grain. 4.48. FiTCHETT.- — Physiological Action of Tutin. 341 P.M. 4.8. Is tremulous and unsteady. 4.14. Slight convulsive movements, affecting the wings and head ; vomiting. 4.20. Vomiting. 4.25. Defecated ; a more severe convulsion ; body bent forward till breast touches ground, head bent back, wings rigidly extended, perhaps one more than the other. The bird was here taken out of the cage and placed on the floor of the laboratory ; it did not attempt to fly away, and kept pretty much to the place where it was set dowia ; it moved away a little if approached. On the whole, seemed more acute mentally than birds that had received a larger dose. 4.28. Convulsion, but still able to keep its feet ; pupils widely dilated during convul- sion. 4.33. Retching. 4.35. I 4.36. \ Convulsions. 4.361 J 4.38. Vomiting and convulsions. 4.39. Convulsion, still affecting chiefly the fore part of the body. 4.42. Vomiting and convulsions ; pupil continuously dilated. 4.46. Most severe con\iilsive attack yet, tail involved, and clonic as well as tonic spasm present. The bird was thrown dowTi, but recovered its feet again. 4.49. Retching. 4.50. ) 4.51. Convulsion. 5.10. Since last note have been frequent convulsions, affecting the neck, wings, and tail, but the bird has kept its feet. They are getting more severe, and last longer. 5.12. Most severe convulsive seizui'e, bird tumbling and somersaulting about the floor of the laboratory. 5. 14. Lying on back ; all the muscles in constant clonic spasm. 5.16. Short interval, during which voluntary squeaking. 5.20. Lying on back ; convulsions continue ; legs as much affected as wings. 5.42. Has been lying on back in constant movement since 5.16. 5.51. Movements becoming more feeble ; they never entirely disappear, but increase in severity at intervals. In the intervals, gasping inspirations. 6.2. All movement ceased ; dead. Result. — Death in 136 minutes from a dose of 12 mlgm. per kilo. Exp. 25. P.M. Pigeon (adult). Weight, 386 grams, 4.45. Gave 15-7 minims of 0-5-per-cent. solution tutin (12 mlgm. per kilo), per os. 5.30. Lying on back, in continuous convulsive movement. 5.31. All movement ceased ; dead. Result. — Death in 46 minutes from a dose of 12 mlgm. per kilo. Exp. 26. P.M. Pigeon (adult). Weight, 305 grams. 5.52. Gave 9-3 minims of a 0-5-per-cent. solution tutin (9 mlgm. per kilo), per os. Next day, 4 p.m. Quite normal. Displayed no marked symptoms. Result. — Recovery from a dose of 9 mlgm. per kilo. Exp. 27. P.M. Pigeon (adult). Weight, 365 grams. 4.30. Gave 11-7 minims of a 0-5-per-cent. solution tutin (9-5 mlgm. per kilo), per os. Next day, 4.30 p.m. Quite normal. Has displayed no marked symptoms. Result. — Recovery from a dose of 9-5 mlgm. per kilo. Exp. 28. P.M. Pigeon (young). Weight, 330 grams. 4.45. Gave 11-2 minims of a 0-5-per-cent. solution tutin (10 mlgm. per kilo), per os. 5.10. Lying on back in convulsions. 5.30. Dead. Result. — Death in 45 minutes from a dose of 10 mlgm. per kilo. 342 Transactions. Exp. 29. P m_ Pigeon (adult). Weight, 368 grams. 4.56. Gave 10-6 minims of a 5-per-cent. solution tutin (10 mlgm. per kilo), per os. 5.14. Vomiting. 5.21. Slight convulsive movements of wings. 5.45. Restless. 8.30. Apparently normal. Result. — Recovered from a dose of 10 mlgm. per kilo. Exp. 30. P ji. Pigeon. Weight, 315 grams. 2.50. Gave ir2 minims of a 0-5-per-cent. solution tutin (10-2o mlgm. per kilo), per os. 3.18. Tremulous; jerking of head ; restless; blinking. 3.20. Tonic spasm of wings ; paroxysms of difficult breathing, during which bird turns round and round in one place. 3.40. Retching. 3.48. General convulsion, lasting 30 seconds, in which bird tumbles about in every direction. 3.51. Lying on side, trembling and breathing very rapidly ; pupils normal. 3.53. General convulsion ; pupils wide. 3.54. General convulsion. 3.56. Recovered upright position, and sat for a few seconds on its tail ; was then seized with severe convulsions, which continued without intermission till death. 4.5. Died. Exps. 31, 32. (See text.) Exp. 33. P_5i_ Lizard (Lygosoma moco). Weight, 4 gi-ams. 5.15. Gave 3 '4 minims of a 0'01-per-cent. solution tutin (5 mlgm. per kilo), under the skin of the abdomen. 6.15. Apparently normal. 7-10. Quiet when first seen ; then took tits of abnormal activity, contorting itself, hold- ing its fore limbs wide stretched, and resting on belly. 7.55. Lying quiet, with mouth partially open. 8.5. Seems quite dead ; mouth still more widely open. Exp. 34. pji. Lizard. Weight, 5 grams. 3.0. Gave 2-5 muiims of a 0'01-per-cent. solution (3 mlgm. per kilo), under the skin of the abdomen. The breathing became exaggerated almost immediately, and the animal puffed itself up as a frog does. 7.30. Nothing remarkable has been noticed. Next day, 9 a.m. Apparently normal. Exp. 35. pyi Lizard. Weight, 7 gi'ams. 4.35. Gave 5 minims of a 0'01-per-cent. solution of tutin (4 mlgm. per kilo), hypo- dermically. 7.20. Remarkable convulsive effects, opisthotonus and twisting into a ball with tail up to mouth, then clonic spasms of limbs ; after this was quiet for a time, and then movements began again ; lies on back biting at its own tail and hind limbs. 7.45. Has been quiescent for last five minutes ; now puffing itself up ; lying in normal position. 7.58. Another severe fit coming on suddenly ; animal twists rapidly into every possible attitude. 8.2. Still in constant movement, now more often on its back. 8.15. Quieter again. 8.25. Another period of restlessness. 8.35. Has quiet intervals. 8.55. Occasional movements. 9.15. Seems quite dead, but gave reflex response from limbs, and did not move after that. FiTCHETT. — Physiological Action of Tiitin. 343 Exps. 36, 37, 38. Thi-ee frogs (Hyla aurea). Weights: (1) 27-5 grams (Exp. 36); (2) 28-4 grams Jan. 15. (Exp. 37) ; (3) 33-7 grams (Exp. 38). P.M. 4.25. Gave to frog (1), 4-1 minims of 0'01-per-cent. solution tutiu (1 mlgm. per kilo); to frog (2), 3'4 minims 0'025-per-cent. solution tutin (2 mlgm. per kilo) ; to frog (3), 6-8 minims 0'025-per-cent. solvition tutin (3 mlgm. per kilo). In each case the solution was injected into the abdominal cavity, and the frogs placed vmder bell-jars on the laboratory-table. 7.30. Frog (3) seems affected ; crouches in a sitting-position, and is blown out with air. No apparent abnormality in frogs (I) and (2). 10.0. No sign of convulsion in any when stimulated. Frog (3) seems more excitable than the others. Jan. 16. A.M. 8.55. All three appear to be affected ; are sluggish, and lying prone on their bellies, with legs extended. Frog (2) is almost dead. 10.0. Frog (2) dead (2 mlgm. per kilo) ; died between 9 and 10 a.m. Jan. 18. Frog (1) found dead in the morning (1 mlgm. per kilo) ; weight, 18 grams, a loss of 9 grams. Frog (3) (3 mlgm. per kilo) is still alive, and seems quite normal. No sign of convulsion noticed in these frogs. The two that died seemed extremely thin and emaciated. Frog (1) looked very much thinner on the 17th than on the two days before. The weather was cold on the 16th. On the 17th the temperature was 12° C. in the morning, but this does not explain why frog (3), with 3 mlgm. per kilo, seems unaffected. Loss of weight might be due to drying ; but the air has not been drj'. The weather is cold and wet. Exps. 39, 40, 41. Thi-ee frogs. Weights: (1) 17-3 grams (Exp. 39); (2) 25-1 grams (Exp. 40); Jan. 16. (3) 32 grams (Exp. 41). P.M. 4.40. Gave to frog (1), 2-6 minims of a 0'01-per-cent. solution tutin (1 mlgm. per kilo) ; to frog (2), 7"5 minims of a 0"01-per-cent. solution tutin (2 mlgm. per kilo); to frog (3), 5-7 minims of a 0-025-per-cent. solution tutin (3 mlgm. per kilo). In each case the solution was injected into the abdommal cavity, and the frogs placed under bell-jar on the laboratory- table. 10.0. No change observed. Jan. 17. No change observed. ,, 18. Frog (2) was foimd dead in the morning ; weight, 18 grams. Weather cold. Frogs (1) and (3) were ajiparently normal. In the two experiments above, the number of minims m 1 c.c. was taken as 15 ; in the subsequent experiments as 17. The doses per kilo body- weight above are therefore smaller than as stated. Exps. 42, 43. Two frogs. Weights : (1) 31 grams (Exp. 42) ; (2) 41 grams (Exp. 43). Jan. 21. P.M. 5.0. Gave to frog (1),- 4 minims of a 0"05-per-cent. solution tutin (4 mlgm. per kilo). 5.15. Gave to fi'Og (2), 7 minims of a 0-05-per-cent. solution tutin (5 mlgm. per kilo). In each case the solution was injected under the skin of the back, and the frogs were placed imder bell-jars, with moist grass and earth, in a cool dark cellar. 7.30. Frog (1) gave a long cry when touched; seems very excitable. Frog (2) apparently normal. 10.30. Could detect nothing abnormal in either. Jan. 22. A.M. 9.30. Both apparently well. P.M. 2.30. Both quite normal. Jan. 25. Quite normal. WiAl 344 Transactions. Exp. 44. Jan. 22. Frog. Weight, 40 grams. P.M. 3.0. Gave 9-5 minims of a 005-per-cent. solution tutin (7 mlgm. per kilo), injected under the skin of the back. The frog was placed under a bell-jar, with wet gi'ass, in a cool cellar. 4.45. Api^arently normal. 6.30. No obvious effect. 10.30. No obvious effect. Jan. 23. A.M. 9.0. No obvious effect. P.M. 4.30. No obvious effect. Jan. 25. A.M. 9.30. Apparently quite normal. Exp. 45. Jan. 28. Frog. Weight, 18 grams. P.M. 3.35. Gave 5'5 minims of a 0"05-per-cent. solution tutin (9 mlgm. per kilo), injected under the skin of the back. It was placed in a cellar, with moist grass and earth. 6.10. Not normal ; squats fiat on belly ; muscular weakness of hind legs ; respiration exaggerated. 7.30. Hind limbs show spastic spasms ; unable to progress ; lies sprawling on belly. Jan. 29. A.M. 10.45. Seems much improved ; sits in normal position ; hops away unsteadily when touched. Jan. 30. Seems weak, but in other respects is quite normal. Exp. 46. Jan. 29. Frog. Weight, 38 gi-ams. P.M. 5.33. Gave 13 minims of a 0*05-per-cent. solution tutin (10 mlgm. per kilo), injected under the skin of the back. It was placed in a cool cellar, with moist grass. 6.10. No change. 7.9. Apparently vinaffected. 9.40. Frog foimd in severe spasm, chiefly affecting the hind limbs, which are fully extended ; is very excitable ; gave cries when touched, and climbed to the top of the bell-jar ; no muscular weakness manifest. Jan. 30. A.M. 9.0. Very lively and excitable ; no distinct convulsions when touched ; is still noisy. P.M. 2.30. Just dying ; mouth open ; could not obtain reflexes. 3.15. Dead. Exp. 47. Frog. Weight, 36 grams. Jan. 31. Gave 11 minims of a 0'05-per-cent. solution tutin (9 mlgm. per kilo), injected imder the skin of the back. It was placed in a cool cellar, with moist grass. Feb. 3. Quite normal. Exp. 48. Feb. 3. Frog. Weight, 31 grams. P.M. 6.15. Gave 10*5 minims of a O'Oo-per-cent. solution tutin (10 mlgm. per kilo), injected imder the skin of the back. As before, it was placed in favourable surround- ings. Feb. 4. P.M. 3.45. Seems weak, but shows no marked symptoms. Feb. 5. Apparently quite normal. FiTCHETT. — Physiological Action of Tutin . 345 Exps. 49, 50, 51. Three frogs. Weights : (1), 23 grams (Exp. 49) ; (2) 39 grams (Exp. 50) ; (3), 30 grams Feb. 18. (^^P- ''^- P.M. 6.20. To frog (1) was given 7 minims of a 0-05-per-cent. solution tutin (9 mlgm. per kilo). ().24. To frog (2) was given 13'2 minims of a 0-05-per-cent. solution tutin (10 mlgm. per kilo). 6.31. To frog (3) was given 11-2 minims of a O'OS-per-cent. solution tutin (11 mlgm. per kilo). Ill each case the solution was injected under the skiu of the back, and the frogs were placed in favourable suiroundings. Feb. 19. P.M. 4.0. Frog (1) affected; Ij'iug prone on belly, with legs extended ; great muscular weakness. Frog (2) presented the same appearance. Frog (3) was found dead at 9 a.m. Feb. 20. Frogs (1) and (2) apparently normal. ■ ,, 21. Both frogs quite well. Exp. 52. Feb. 20. Frog. Weight, 40 grams. P.M. 5.0. Gave 14 minims of a 0-05-per-cent. solution tutin (10-25 mlgm. per kilo). The solution was injected undei the skin of the back, and the frog placed in a cool cellar, with moist grass and earth. Feb. 21. P.M. 2.0. Sprawling on belly ; hind legs extended ; abdomen distended ; twitching of toes ; fibriliary twitching of muscles of thighs. On being handled, was seized with a convulsion, affecting chiefly the hind legs ; the mouth was opened wide and kept open, the animal croaking loudly. 4.25. Dead. Exp. 53. P.M. Pigeon. Weight, 335 grams. 5.30. Gave 5-6 minims of a 0-o-i3er-cent. solution tutin (5 mlgm. per kilo). The injec- tion was made under the right wing. 5.45. Very sleepy-looking ; narcotic effect is most marked ; tremulous about head ; retching. 5.50. General convulsions. 6.5. General convulsive movements have continued since last note ; are now becoming feebler; bird on its back. 6.12. All movement ceased ; dead. Result. — Death in 42 minutes from a hypodermic dose of 5 mlgm. pei kilo. Exp. 54. P.M. Frog. Weight, 20 grams. 4.55. Gave 6-8 minims of a 0-1-per-cent. solution tutin (20 mlgm. per kilo), under the skin of back. 5.0. Breathing exaggerated ; keeps opening mouth wide. 5.15. No further .symptoms ; gave other 7 minims. 5.16. Rapid breathing ; mouth-opening movements. 5.26. Gave other 7 minims. 6.0. Lying prone on belly ; shows occasional slight twitchings, chiefly of hind legs ; if touched, is seized with conv^ulsions, and pupils dilate ; respirations irregular and exaggerated ; makes a sucking noise occasionally. 6.9. Turned on back ; cannot recover, and struggles violently and continuously in its efforts to do so. 6.11. Most severe convulsions; mouth spasmodically opened to fullest extent; cries loudly ; spasms occur every 4 or 5 seconds. (This change has occurred since, and apparently as a result of, violent voluntary efforts to recover position when placed on back.) Heart can be seen beating through abdominal wall ; rate, 44 per minute. 346 Transactions. P.M. 6.15. Respirations ceased. 6.20. Heart-movement not so visible ; rate, 32 per minute. ]\Iuscles still show occa- sional twitches and spasms. 6.30. Seems quite dead ; no reflexes. This frog received about 60 mlgm. per kilo. Exp. 55. p jj Frog (female). Weight of frog, 38 grams ; ovaries, 57 grams. 4.12. Gave 1 minim saturated solution tutin. injected under skin of back. 4.30. Remains crouching ; if turned on back, recovers position slowly. 4.35. Turned on back ; recovers position with difhculty ; convulsive movements fore and hind limbs ; lies prone on belly ; if legs extended, does not retract them ; respiration feeble and irregular ; convulsive movements of limbs if turned on back. 4.40. Attempted to crawl, but unable to advance ; pricking skin of limb, no response. 4.45. Respiration imperccjjtible ; if turned on back, recovers position with dilhcidty, then tonic spasm in extension and a few vigorous respirations. 4.55. \\Tien turned on back, quickly recovered, and made three or four vigorous hops ; crying loudly, with jaws spasmodically 0]>ened, then lay on belly, and at inter- vals of 10 to 15 seconds opened jaws widely and extended limbs in tonic spasm. 5.15. \Mien turned on back, laj' so, occasional tonic spasm of fore limbs, irregular feeble movement of hind limbs ; respiration at rare and irregular intervals — two or three respirations, and then a more or less prolonged pause ; helpless, lying on belly, reflexes still present ; makes no attempt to swim when placed in water ; unable to rectify position in water ; lying on back at bottom of basin. 6.7. Under bell-jar, makes occasional kicking-out movements ; still on belly, and swollen-looking. 7.40. Very similar ; makes less movement than before ; lies in practically any position if gently handled, but reflex action still marked ; pupils dilated. 10.15. No spontaneous movement, and no reflexes (some movements, got on turning over or letting fall, seem due to direct stimulation of muscles) ; pupils dilated ; no respiration seen. Next day, 9 a.m. Dead ; stifl: in position it was in for greater time after injection. Exp. 56. P.M. Frog (small). 3.0. Gave 1 minim semi-saturated solution tutin, injected under skin. 3.3. Attempting to jump, but movements already enfeebled. 3.15. Respiratory movement exaggerated ; abdomen distended. 3.20. Slowly extended hind legs and advanced fore legs, and lay on belly ; respiration quickened and exaggerated ; occasionally raises fore part of body in spasm to full extent of fore arms, and respiration ceases. 3.25. Twitching of toes. 3.35. Attempting to crawl flat on belly ; unable to make progress ; conjunctival reflex active ; skin reflex sluggish ; pupils dilated. 3.40. Spasm of all four limbs ; restless; raises body stiflSy, with hind limbs extended. 3.45. Continuous struggling-movements ; twice turned on back, and slowly and with difficulty recovered position. 3.50. Placed on back, unable to recover ; twitching of muscles and successive tonic spasms ; respiration rare and convulsive ; has opened mouth spasmodically once. 4.10. Reflex action abolished, except conjunctival, which is sluggish. 4.15. Repeated spasmodic opening of mouth. 4.. 30. Can still see ; lies on back ; occasional movements of fore limbs. 5.5. On letting fall, slight reflex in fore limbs ; conjvmctival reflex still present. Exp. 57. P.M. Frog (small). 4.30. One drop of a semi-saturated solution tutin in conjunctival sac. 4.45. Movements of fore limbs to eyes ; conjunctival irritation ; restlessness ; ex- aggerated respiration. 5.0. Opisthotonic movements ; weakness of liind limbs ; crawls slowly ; hops with difficulty. FiTCHETT. — Physiological Action of Tutin. 347 P.M. 7.5. When light turned on. was foiind to be in a .state closely resembling clonic stage of epileptic fit ; this soon subsided, but could be initiated to a lesser degree by pulling animal about by hind leg. Pupils wide ; respiratory movement excited and irregular. 10.30. Dead. Exp. 58. P.M. Frog (small). Weight, 12*5 grams. 12.35. Gave 1 minim of a 0-05-per-cent. tutin solution in 0'76 per cent, saline, injected mider skin. Motionless, on bellj^. 12.42. First movement, lifted head. 12.45. Sprang forward ; increased respiratory rate. 12.50. Attempted to spring, but moved sluggishly, and did not advance ; emptying of cloaca, urine, and faeces. 12.55. Raised on all four limbs, and sank slowly back on belly. 1.0. Raised himself on all-fours, and remained sitting up with fore limbs extended ; irregular crawling-raovements, chiefly in fore limbs ; feeble attempts to spring ; hind limbs seem weak ; pupils dilated. 1.10. Restless ; attempting to crawl up side of bell- jar ; movements incoordinate and feeble. 1.43. Sitting motionless; pupils more dilated than at beginning of experiment; can leap fairly well when toe pinched, but seems feebler, and does not resent inter- ference so much as in a normal frog. 2.3. Leaning up against side of bell-jar ; left hand partially closed, as if grasping a twig ; right extended against glass. 2.43. Lying quiet ; recovers position fairly quickly when turned on back ; also shows occasional voluntary movements. 3.13. Same; pupils wider than previously. 4.13. As before, but respirations (taken from movement of floor of mouth) 40 for one half-minute, 30 for another half-minute, and rather irregular. 4.50. Lying prone on belly, with legs extended from sides ; if turned on back, recovers with difficulty ; able to advance across table by short halting leaps ; hind legs drawn up slowly to jumping-position after each effort ; no convulsive move- ments noted so far ; seems to be a general muscular enfeeblement. most marked in hind legs. 5.0. Makes continued efforts to jump, but fails to advance, as cannot flex legs suffi- ciently beneath body. CO. Lying prone on belly ; turns over when placed on back, though with difficulty. 7.35. Ljnng sprawling on belly ; limbs extended ; moves feebly when disturbed ; pupils dilated (? due to darkness) ; while being observed it had something like a weak convulsive fit. It lay on belly and kicked out repeatedly but feebly with hind legs, and moved fore limbs as if attempting to swim. 9.35. Sprawling on belly as before, and motionless till distiu'bed. Weakness more marked ; cannot turn over when placed on back ; makes several efforts, accom- panied by deep breathing, and then lies still. Next day, 9 a.m. Found dead, in same position as left in last night ; pupils firmly contracted ; lower limbs extended ; fore limbs flexed, and digits closed, as if grasping twig ; no swelling of abdomen. P.M. — Gall-bladder distended ; intestines distended ; cloaca full ; intestine, some dark grumous licpiid; stomach empty, except for mucus; kidneys apparently normal; no abnormality at seat of injection ; central nervous system nothing abnormal, except seems too pale ; no ecchymosis ; blood seems fluid, and animal as a whole seems more bloodless than normal ; blood-film squeezed out of heart and tissues presents many leucocytes, possibly dvie to mode of obtaining it. Exp. 59. P.M. 5.45. Small trout, in 100 c.a water, with 10 drops saturated solution of tutin (about O'l per cent.). 5.49. Movement very excited ; breathing exaggerated. 6. 18. Breathing more laboured. 6.28. Swimming on side, near s\irface. 6.30. Shuddering- movements ; spasmodic movements of gills, which then ceased. Control, in same amount of water, showed no change. Exps. 60 to 76. These experiments were very like the above (see Table III). 348 Transactions. Table of Experiments on Fishes. 6 Per- o "S . Drug. centage of Modification of Drug. S!S •2 2 Time of OiLset of Symptoms. Result. Time of Death. ^ Drug. ■gER h^ f^ > ^ C.c. 77 Tutin 0001 200 Died . . 4 hours. 78 0-00075 200 5 hours 6i „ 79 0-005 200 ^ 5 „ 6 „ 80 Picrotoxin 0-001 200 )) 4 „ 81 0-00075 200 5 hours 6 „ 82 )) 0-005 200 li .. J3 • • 4 „ Control to the above fishes under the same conditions (200 c.c. fluid) showed symptoms of asphyxiation in 4 hours, and the fishes in tutin and picrotoxin died practically in order of their weights. d Per- o o . ft Drug. centage of Modification of Drug. ume 'luid n Time of Onset of Symptoms. Result. Time of Deatli. X Drug. > ■ C.c. 83 Tutin 0-001 ^ . 1,000 3 9^ hours Recovered 84 Tutin and chloral 0-001 ) 0-128 i 1,000 3 Not observed . . 1 died . . About 22 hours. 85 Picrotoxin 0-001 1,000 3 9 J hours »» • • *) 86 Tutin 0-0015 1,000 3 1 horn- )> ■ " 1| hours. 87 »» • • 0-00125 1,000 3 No symptoms All lived 88 »» • • 0-00175 1,000 3 4A hours (1.) 2f hours.. 1 died . . Died . . 4| hours. 7 hours. 89 >» • • 0-003 1,000 (m.) 9J „ . . >J • • 12 i (s.) 10 „ .. i» 11-23 „ 90 »> • ■ 0-002 1,000 3 No symptoms (1.) 4 hours . . (m.) S 11 g li t s y m p 1 0 m s All lived Died . . Recovered 4i hours. • • 91 )) 0-0035 1,000 3 - from 7-10 hours (s.) No symp- toms 0-0035 -' Digested with HCl 30 min. and then neutralised 1,000 (1.) 3J hom-s . . ) Fatal ( (1.) 7i hours. 92 ») • ' 3 (m.)8i „ .. (s.) 9 „ .. to - 1 all I (m.) 10-22 „ (s.) 22* „ 93 »J • • 0-003 ( Already once used, filtered H y d r 0 1 ysed 1,000 1 1* ( 4| hours (1.) 5 hours . . Died . . Died 6f hours. 25J „ 94 >f • * 0-004 ■! with HCl 1 r 1,000 3 \ (m.)6i „ .. 3 J • • 28 ,, (A) I hour at 37° C. 1 ( (s.) 8 „ .. Recovered ( 0-004 " Control to 94 ; ' (l.i 31 „ .. Died . . 12 hours. HCl added, (m.)8 „ .. »» • * H ; 95 l» * * and imme- -1,000 3 J {s.)SUght symp- Recovered (B) diately neu- toms at 12 , tralised hours 96 )» • • 0-004 Treated with 1,000 3 No symptoms All lived (0) 0-2 per cent. XaOH for 1 hour at 37° C. 0-004 - - 1,000 ■ (1.) 3 hours Died About 16 hours. H y d r o 1 vsed (m.) Symptoms )) ■ ■ „ 22J „ 97 »» • • with HCl 1 3 - at 16 hours (A) hour at 37° C. (s.) No symp- Lived . . , , toms 98 »» • • 0-004 Control to A. 1,000 3 2 hours All died About 16 hours. (B) HCl imme- dately neu- tralised 99 »» • ■ 0-004 Treated with 1,000 3 No symptoms All lived (C) 0-2 per cent. NaOH for 1 hour at 37° C. (1.) 3ihoiu-s.. Died 29J hours. 100 Picrotoxin 0-004 1,000 3 ■ (m.) 3i „ . . ») * • 12 „ (s.) 6J „ .. J) • • 12 ., * Fish used In this experiment was Cheimarrichthys fosteri. fatal to three minnows. Tutin solution, 0-003 per cent., was not FiTCHETT. — Physiological Action of Tutin. 349 Table of Experiments on Fishes — continued. d Per- o Drug. centage of Moditication of Drug. a-6 Time of Onset of .Symptoms. Result. Time of Death. Drug. r biM 1 Co. 101 Tutin 0-005 Treated with 0-2 per cent. NaOH for 20min. 1,000 3 Xo symptoms All lived 25 hours ■ 102 %> 0-005 Treated with 02 per cent. NaOH for 1,000 3 No symptoms All lived 25 hours 40 min. 103 »» 0-005 - Acted on by living liver- cells for 1 hoiu-at37°C. Acted on by living kid- ) :- 1,000 j ( 3 I ( (1.) 2} hours.. (m.)2i „ .. (s.) 4i „ .. (1.) li hours. . I All ( j died ■ Ditto - 5 J hours. 6' „ 7 J „ Of hours. 104 i „ 0-005 - ney-cells for - 1,000 3 (m.) 2j „ .. 7i „ 1 hour at i (s.) 4J „ .. 27 37- C. '\ (1.) U „ .. 1 J 3 105 Picrotoxin 0-0132 . , 1,000 (m.) IJj „ . . 6J „ ( (s.) 1 „ .. ) " I 2i „ ) i (1.) 7i „ .. ) 1 About 22i hrs. 106 ' Tutin 0-005 1,000 3 ( (m.) 6J „ . . 23 hours. (s.) 7i „ .. ) " 1 About 22i hrs. 3i (1.) If „ .. ) 1 3.V hours. 107 Picrotoxin 0-005 , , 1,000 (m.) If „ . . Hi „ ( (s.) If „ .. 1 " '( 12s ,. 108 Tutin 0-005 ' Had been used once before [ 1,000 3-1 ( (1.) 2| „ .. (m.) 4? „ . . (s.) H „ .. Recovered Died . . 12| hoiu-s. 12i-25 hours. 109 »» • • 0-005 Treated with 02 per cent. 1,000 3 No symptoms All lived 30 hours -• ! NaOH for 10 minutes 110 j» • • 0-005 I Ditto Treated with 1,000 ) 3 )) Ditto . . 0-2 per cent. ( (I.) 6f hours.. ) ( - All died j 135 hours. 111 »r • • 0-005 J HCl for 1 1- 1,000 3-' (m.) 5i „ . . sl „ hour at 37^ j i C. ) ( (s.) 5i „ .. 9J „ 112 it • • 0-005 Treated with 0-2 per cent. NaOH for 5 minutes at 37° C. 1,000 3 No symptoms All lived 26 hours Fluids 94 (A), 95 (B), and 96 (C) filtered and tried over again. (1.), (m.), (s.) = large, medium, small. A.M. 8.43. 9.40. 11.. 30. 11.50. P.M. 12.10. 12.49. 1.5. 2.15. 3.10. 3.22. 4.0. 5.0. 6.20. 7.20. Exp. 108. Three minnovt's (large, medium, and small). Placed in 1,000 c.c. fluid of 0-005-per-cent. solution. Xo symptoms. Large fish on side, emitting air-bells. Large fish now upright, but keeping near surface. Large fish on its side ; movements feeble. As yet the otiiei- two fish are un- affected. Large fish upright again ; near surface. Large fish on side near surface. Medium fish in excited movement near surface, emitting air-bells. Small fish excited. Large fish same ; medium and small both on the side near the surface. ■ Same. All markedly affected, and keep more or less on side, near the surface. Same. All swim near surface, excitable, but feeble ; now swimming upright. All keep close to surface, and emit air-bells. 350 Transactions. P.M. 8.20. Gill-movements have ceased in medium-sized fish ; heart-movement still visible. Large and small fish both deeply affected. 9.15. Large fish dead. Small fish deeply affected ; swimming upright, but very feebly, near surface. Next day. Small fish apparently well. P.M. Exp. 114. 3.55. Two cockles, of about the same size, were placed — one in sea-water, the other in a 0-5-per-cent. solution of tutin in sea-water. Equal volumes of fluid were used. 4.0. The cockle in tutin solution has opened its shell. 4.10. The cockle in sea-water has not moved. The one in tutin solution keeps opening and closing its shell at intervals of a minute or two. 4.15. Portion of the one in tutin solution is now extruded from its shell ; the shell every now and then shuts down sharply, but without the extruded portion being drawn back ; when touched with a needle the extruded portion is with- drawn, but is pushed out again after a short interval. 4.25. The one in tutin solution continues extruded, but withdraws when the glass container is tapped with a pencil. Next da3^ 9 p.m. The one in tutin solution is dead ; throughout the day it has remained with shell open and body extruded ; at noon to-day was alive, and withdrew sluggishly when touched with a needle. The one "in sea-water is still alive, with the shell firmly closed ; it has not been observed to open the shell through- out the experiment ; on being ]ilaced in the tutin solution it opened its shell in a few minutes, and behaved as the other had done. Exp. 115. Jan. 21. At 8 p.m. two flies — a large blowfly and an ordinary house-fly — were placed in a cage with a watch-glass containing a solution of sugar in a 0-1-per-cent. solution tutin. Both were observed to partake freely of the solution on several occasions. ,, " 22. At 8.30 p.m. both flies are active, and apparently quite normal ; they fre- quently feed from the watch-glass. ,, 23. At 12.15 p.m. the house-fly is dead. The blowfly is active, and apparently normal. ,, 24. Blowfly quite well ; allowed to escape. Exp. 116. Mar. 1. About twenty house-flies were placed in each of two cages. Into one cage was put a solution of sugar in a 01-per-cent. solution tutin m normal saline; into the other a solution of sugar in normal saline. The flies, being thirsty, at once crowded rormd both watch-glasses, and partook freely. ,, 4. All the flies are alive, and quite healthy. The flies with the tutin solution do not feed so readily as those with the normal saline ; they frequently approach the watch-glass, merely taste the solution, and retire ; now and again one will remain feeding. ,, 7. Flies still all alive, and quite healthy ; diu'ing the week the solution has dried lip once or twice, and more 01-per-cent. solution tutui has been added. Despite the concentration by evaporation, they have displayed no symptoms. P.M. 6.40. A few drops of 0-5-per-cent. solution tutin in distilled water added to the watch- glass, which had become dry. 7.0. On returning, found four flies on their backs, but not dead ; moving their lega occasionally. Three other flies were affected. Every now and then wings violently buzzed for a second or two, lifting flies on to tip-toes. They walk rather incoordinately. 7.5. One of the affected flies spinning round and round on its back, wings buzzing continuously ; movement ceases for a short interval, and is then repeated. 7.8. Both the other flies similarly affected. 7.15. All three are now lying quiescent on backs, with occasional movements of legs. Mar. 8. A.M. 10.0. Ten flies dead ; several others seem unaffected. A large blowfly introduced into the cage, and observed to drink the solution for 15 minutes. 10.30. Blowfly not so active ; does not fly away when probed ; shows what seem to be involuntary movements of the legs. FiTCHETT. — Physiological Action of Tutin. 351 A.M. 10.40. Blowfly very lethargic ; walks heavily ; can be pushed along without offering to fly ; every now and then one or other wing extejided to full extent, and held there a moment ; this is not a voluntary movement ; does not seem to have proper control of legs when walking — one or more legs move irregularly, and not in a suitable direction. 11.0. Blowfly allowed to escape from cage ; remained in one position on table till touched, and then flew heavily on to window, crawled into a corner, and was siibsecpiently lost sight of. Two other blowflies introduced into cage ; one immediately fed from the watch-glass, and in 15 minutes showed symptoms; lethargic, and disinclined to move. P.M. 12.0. Second blowfly has been observed to drink but sparingly. First blowfly show- ing moie marked symptoms ; tonic spasms of wings and uncontrolled move- ment of legs ; allowed to escape, but on attempting to fly seized with a general convulsion, buzzing round and round on back ; was attacked with seizures of this kind imtil exhausted. 1.0. Lying on side, dead. Quite a considerable drop of clear fluid has exuded from proboscis. Mar. 10. All the house-flies are dead, and all show marked distention of abdomen. Blowfly apparently luiafl'ected, so allowed to escape ; flew about on window for few minutes, and was then seized with convulsions and died, as the others had done. Exp. 117. Jan. 30. At 4.30 p.m. some mince was allowed to become infected by blowflies. A small portion of the meat containing the larvae was placed in each of four watch-glasses, and covered with a 001-per-cent., a 0025-per-cent., and a 005-per-cent. solution tutin, and with normal saline respectively. In each case the larvae began to wander and coil up in the fluid. After one hour these fluids were poured oft', and each watch-glass covered with another, to prevent evaporation. ,, 31. At 4.45 p.m. the watch-glasses were examined. In the one treated with normal saline only the larvae ai'e numerous, have grown, and are very active, crawlmg all over the surfaces of both watch-glasses. In the 001-per-cent. and 0.025-per-cent. solution only one or two larvae are to be seen in move- ment ; they are very small, and have not wandered from the mince. In the 005-per-cent. solution no movement is to be seen. Exp. 118. A drop of hay-infusion, containing paramcecia, amcebae, monad.?, and bacteria, was placed on each of four slides, labelled A, B, C, D. P.M. 5.49. One drop normal saline added to B. 5.50. One drop of a 01-per-cent. solution tutin in saline added to C. 5.51. One drop of a 01-per-cent. solution quinine hydrobromate in normal saline added to D. 6.5. B : No change. C : No change. I) : No paramcecia to be seen, but monads and bacteria still moving. 6.30. B : No change. C : Paramcecia may still be seen moving, but their move- ments are irregular ; the monads are collecting at the surface and edge of the drop; this may also be seen in A and B. Another drop of a 01-per-cent. solution added to C. D : No movement. 6.50. A and B : No change. C : Still one or two paramcecia moving ; are not so easy to find ; many monads still active, others stationary ; amoebae still moving ; field does not look .so lively as it did. Exp. 119. 7.30. A drop of hay-infusion placed on a slide, and covei-ed with a cover-glass, and a drop of a 01-per-cent. solution tutin normal saline placed at edge of cover. 7.35. 8ome paramcecia have swum out into dro]i of tutin solution ; at once display irregular movements ; remain in the drop of tutin solution. 7.40. Movement of paramcecia in drop of tutin solution, which at first were excited, now becoming slower and very irregular ; they roll over and over like rotifers. 7.45. Paramcecia at a standstill in tutin solution : they appear to disintegrate in- ternally, and are no longer recognisable ; paramcecia under the cover-glass quite normal. Experiment repeated, using a 0-5-{3er-cent. solution tutin in distilled water, with similar results. 352 Transactions. Exp. 120. This experiment was essentially similar to Exp. 119. Exp. 121. Jan. 28. Six test-tubes wei-e taken and labelled — '' 0-5 per cent, tutin," " 0-4 j^er cent, tutin," "0-3 per cent, tutin," "0-2 i^er cent, tutin," "01 per cent, tutin," and " normal saline." The volume of fluid in each tube was the same. P.M. 5.0. A small piece of fresh mmce was added to each tube, and the tubes left open to the air. Jan. 29. At 5-45 p.m. the tubes were corked, and placed in an incubator at 40° C. „ 31. Tubes opened and examined. The tube containing normal saline was very- offensive. None of the other tubes had the offensive smell of putrefaction ; the smell was rather like that of stomach-contents. Feb. 1. Contents of tubes examined under microscope ; all show moving bacteria, but the drop taken from the tube containing normal saline was much more crowded, and the bacteria in it showed a gi-eater variety of form and size. Exp. 122. Four fermentation-tubes were filled — (1) with glucose solution and tutin (0-25 per cent, of the latter) ; (2) glucose solution, with 0-1 per cent, tutin ; (3) glucose solution alone ; (4) water. A few drops of a yeast emulsion were added to each. P.M. 5.45. Tubes placed in inciibator. 7.10. Fermentation in (1) and (3). 7.45. Fermentation in (2) as well, but only half as much gas developed as in (1). 9.30. (]), (2). and (3) fully fermented. Exp. 123. 4.40. Two fermentation-tubes set on — (1) with glucose alone ; (2) with 0'05 per cent. tutin. 5.10. No change. 6.10. Both equally fermented. 8.30. Both fully and equally fermented. Exp. 124. Four fermentation-tubes filled with the following : — A : Water (16 o.c), 25 per cent, glucose (4 c.c.) ; B: Water (20 c.c.) ; C : Water (8 c.c), jilus 0-5 per cent, tutin solution (8 c.c.) plus 25 per cent, glucose (4 c.c.) (equals 0-2 per cent, tutin in mixed fluid); D: 0-5 per cent, tutin (16 c.c), plus glucose (4 c.c.) (equals 0-4 ])er cent, tutin in mixed fliiid). A few drops of freshly procured emulsion of brewers' yeast added to each ; D received rather more than the others. P.M. 3.30. Tubes placed in incubator. 4.40. Small bubbles forming in A, C, and D. 5.10. Same. 6.0. Fermentation most distinct in D. 7.10. Most fermentation in D ; slight in C ; little or none in A and B. 7.30. Added another drop of yeast emulsion to A. 8.0. Fermentation now as great in A as iii D. This shows that the amount of yeast added exerts a greater influence on the amount of fermentation that occurs than does the presence of tutin. Exp. 125. Five test-tubes were taken, containing a 0-1-per-cent., a 0-2-per-cent., a 0-3-per- cent., a 0-4-per-cent., and a 0'5-per-cent. solution tutin in normal saline ; and one test-tube containing normal saline alone. Equal volumes of fluid in each test-tube. Jan. 23. At 4.30 p.m. twelve miistard-seeds were placed to soak in each test-tube. ,, 23. At 4.30 p.m. the seeds from each test-tube were sown on moist felt placed in separate tin boxes, correctly labelled. ,, 24. All the seeds in each box have germinated. ,, 25. At 10.10 a.m. the same progress has been made in each case. All the seeds were replaced in their respective sohitions. Fttchett. — Phijsiological Action of Tutm. 353 J a 1. 26. The seeds were resown in the tin boxes. ,, 30. All have grown more or less. The seeds soaked in normal saline have made- most progress, and ai-e closely followed by those soaked in 0-1 per cent, and 0-2 per cent. Those soaked in 0-4 per cent, and 0-5 per cent, are growing, but only two or three seeds in each, and the growth is not so vigorous as in the others. Since the 26th the felt in the boxes has been kept moist by the addition of water. Feb. 3. All the seeds soaked in normal saline have grown, and are growing vigorously. In the boxes labelled ''0-1 per cent." and "0-2 per cent." three or four seeds are growing vigorously, and have made nearly as much progress as in the box labelled " normal saline," but the others remain stunted, and one or two have made no progress since being resoaked in the tutin solution. In the boxes labelled "0-4 )ier cent." and "0'5 per cent." one or two seeds have made good progress, but most of the others are stunted, or have not grown at all. Exp. 126. A few bars were taken from the gill of a cockle, and mounted in sea-water, and observed xnider the low power. P.M. 4.0. Normal saline perfused under cover-glass. 4.35. No appreciable difference. 4.38. 0-1-per-cent. tutin solution perfused under cover-glass. 4.45. No change. 4.46. 0-2-per-cent. solution tutin perfused under cover-glass. 4.50. Seems to be a slight retardation, but doubtful. 4.51. 0-3-per-cent. tutin solution ])erfused under cover-glass. 4.52. Obvious slowing ; many cilia stationary, others moving feebly. 4.59. Ciliary movement practically ceased. Exp. 127. 5.10. Fresh specimen taken in 0-3 per cent. 5.11. Movements slower. 5.13. Very feeble movement. 5.15. ^lovements ceased. Normal saline and afterwards sea-water were then perfused under cover-glass, biit recovery did not take place. Exp. 128. 5.30. Fresh specimen taken, and a 0-2-per-cent. solution tutin perfused under cover- glass. 5.37. Movements have practically ceased, except for a few cilia here and there. 5.45. All movement apparently ceased. A solution of j-^-^^ KOH in sea-water perfused under cover-glass, and ciliary movement immediately resuscitated. p.m. Exp. 129. 5.54. Fresh specimen taken, and a 0-2-per-cent. solution tutin applied. 6.5. Cilia still moving ; movement confined to the apices of the cilia. A di'op of 0-3-])er-ccnt. solution tutin applied. 6.15. Still moving, but less actively. A drop of 0-5-per-cent. solution tutin applied. 7.30. Still moving. As this piece of gill was rather large, a fresh specimen was taken from a mxissel. P.M. Exp. 130. 7.45. 0-2-per-cent. solution tutin ajjplied. 7.52. A distinct slowing has occuiTed, biit the cilia are still able to cause a movement of particles. This only occurs in sheltered places. The cilia are at a standstill on the edges. 7.57. A drop or two of sea-water applied, and many cilia restored to action. In every case a control mounted in sea-water was used for comparison. Exp. 131. Two or three gill-bars from a small rock-oyster were taken and mounted in sea- water raider a cover-glass. Two preparations were made, and one used as a control. (Low power.) 12— Trans. 354 Transactions. P.M. 2.30. A drop or two of a 0-5-per-cent. solution in sea-water tutin perfused under cover- glass. 2.35. Appears as if there was a slight slowing of cilia in exposed situations, but doubtful. 2.40. Cilia still moving ; more 0"5-per-cent. solution tutin i>erfused under cover-glass. 3.0. Most cilia in active movement ; here and there a few are motionless, or moving feebly. 4.0. Still moving. Exp. 132. A fresh preparation was made from the gill of a cockle, and examined with the low power without a cover-glass. A control was used. P.M. 3.10. A drop of a 0-5-per-cent. solution tutin a))plied. 3.12. If anything, movements seem exaggerated. 3.20. First drop tutin solution dried off. and a second drop added. 3. .50. No effect observable. 4.30. Still in active movement. Exp. 133. i Three preparations of ciliated epithelium from the gullet of a frog. No. 1 was mounted in normal saline without a cover-glass, and used as a control ; No. 2 was moiuited in a drop of a 0-1-per-cent. solution tutin, without a cover-glass: No. 3 was mounted in a drop of a 0-5-per-cent. solution tutin, without a cover- ! glass. Three microscopes were used, and the s])eciraens examined inider the low power, with the draw-tube out. 1. 2, 3. 5.14. Moving. No effect. No change. 5.20. No change. >! 5.25. >» ,, 5.30. )? JJ 5.35. f? 9? 5.40. >» 9J 6.10. The'spe ;cimens had partif illy dried, and only. Exp. 134. The gullet of a frog was exposed, and the rate of progress along it (by ciliary action) of a small fragment of cork was observed. A centimeter scale was arranged to lie parallel with the gullet, and the time the cork took to travel 1 cm. noted as follows : — Gullet bcitlied with Normal. a 03-per-cent. Solution Tutin. 52" 32" 47" 38" 61" 38" 51" 29" 51" 37" Average, .'iO-4" Average, 34-8" Exp. 135. Two frogs' nei've-muscle preparations made. Muscles placed in watch-glasses with normal saline. Nerve laid on frog-plate, and kept moist with saline, and stimulated with break shocks. A (in saline), minimal stimulus found to be with coil at 17 cm. B (in saline), minimal stimulus at 21-5 cm. B was then placed solution tutin in normal saline in a watch- -glass cor^ ^a^ning a 0-025-per-cent at 5.54 p.m. P.M. A. B. 5.55. Contracts at 20 cm. 20 cm. 6.8. 20 cm. 18 cm. 6.17. 21 cm. 19-5 cm. 7.15. 19-5 cm. 18 cm. 7.35. 19 cm. 17 cm. 8.10. 19 cm. 16 cm. 8.52. 18 cm. 15 cm. 9.35. 18 cm. 12 cm. FiTCHETT. — Physiol oy teal Action of Tuhn. 355. Exp. 136. In this experiment, the nerve of the one preparation (A) was i>laced in tiitin sohi tion (0-5 per cent.), and the muscle of the other (B) in the same. Before ])Iacing in tutin solution, A contracts at 28 cm., and B at 34 cm. P.M. 6.3. Tutin solution ajiplied as above. A. B. 6.6. Contracts at 31-5 cm. 28-5 cm. 6.17. „ 30-5 cm. 30 cm. 7.22. „ 33 cm. 27-5 cm. Exp. 137. One muscle in saline (B) and one in a 0-05-per-cent. solution tutin (A). Nerves exposed to air, and kept moist. Stimulated as before. Before tutin applied. A contracts at 30-5 cm., and B at 25-5 cm. P.M. 6.15. Placed in tutin solution. A. B. 6.20. Contracts at 28-5 cm. 25 cm. 6.28. )j 28-5 cm. 24 cm. 7.25. >) 24-5 cm. 22-5 cm. 8.20. >> 25-5 cm. 25 cm. Exp. 138, Same as previous experiment. Before tutin (interrupted current), A contracts at 36 cm., and B at 32 cm. ; single shocks, A contracts at 27 cm., and B at 25-5 cm. A.M. 10-56. A placed in a 0-05-per-cent. solution tutin in normal saline. B left in saline. A. B. 11.2. Contracts at 27 cm. 26 cm. 11.20. »? 26-5 cm. 25 cm. P.M. 12.20. *» 24 cm. 24-5 cm, 1.0. ») 21-5 cm. 23 cm. Exp. 139. Rabbit (young). Weight, 804 grams. Blood-films were taken, dried in the air, and fixed with Jenner's stain ; and next A.M. morning at — 11.36^. Gave 25 minims of a 0-5-per-cent. solution tutin (lOmlgm. per kilo), hypoder- mically. 11-56. Shaking-movements of head ; pvipils normal. 11.58. Shaking and rocking of whole body ; lying prone on belly. 11.59. Twitching of ears. P.M. 12.0. Twitching of hind limbs and then of fore limbs. 12.1^. Severe convulsions; kicking-movements ; head drawn back; clawing-move- ments ; convulsions lasted 2 minutes ; pupils did not dilate ; cornea damaged by rubbing open eye on floor in convulsion. 12.3^. Lying on side, with head bent back ; hind and fore limbs show running-move- ments. Clonic convulsion. Convulsion passed, but running-movements of legs continue. Clonic convulsion. Convulsion passed ; running-movements continue ; head bent well back. Convulsive movements of jaw and ears, gradually merging into a general con- vulsion. Momentary quiescence. Jaw and limb movements continue. The lower jaw is pushed forwards, and then clenched so that lower incisors lie outside upper incisors, then they slip inside the upper incisors with a grating sound. 12.22. Movements still continue ; no cry has been uttered by the animal as yet ; respir- atory movements are not much in evidence ; movement of limbs, jaw, and retraction of head most prominent. 12.4i. 12. 6. 12. ,8. 12. 11. 12. 13. 12. ,15. 12, ,18. 356 Transactions. P.M. 12.32. Same ; lying on left side, with occasional kicking-movements. 12.34. All movement ceased, except that heart can be seen beating by movement of hairs over precordial region. 12.36. Dead. P.M. — Stomach not distended ; contained only food ; blood-film taken from the left ventricle only ; heart had ceased beating ; lungs not congested ; bladder full. Result. — 10 mlgm.. per kilo caused death in less than one hour. Exps. 140-151. Experiments 140 to 151 inclusive referred to the blood-pressure work, details ot which are omitted. Exp. 152. P.M. Cat. Weight, 3-52 kilograms. 3.(). Chloroform administered with a Skinner's mask. The skin was reflected, the cranium trephined over the right parietal region, and the bone removed with bone forceps until the greater part of the right cerebral hemisphere was exposed. 4.10. 50 minims of a 0-5-per-cent. solution tutin was injected hypodermically, and the administration of the anaesthetic discontinued. 4.24. As no symptoms had ajipeared, 25 minims of a 0-5-per-cent. solution tutin was injected into the peritoneum. 4.32. Slight twitching of the head and ears noticed, followed in a minute or two by con- vulsive movements of the paws. The right cerebral hemisphere was imme- diately scooped out. The con-\ailsive movements continued as before, affecting both sides equally. The left cerebral hemisphere was then removed. The convulsive movements continued. The breathing was greatly exaggerated, and at intervals large quantities of urine were shot out with considerable force. 4.45. The spinal cord was then divided at the level of the 5th doi'sal vertebra. 4.49. Spasmodic movements of the hind limbs ; the limbs were rigidly flexed on the abdomen and shaken with clonic spasms. 4.54. Movements of fore paws. ^.56. Slow spasmodic movements of hind limbs, the slow rigid movement towards the abdomen ending in clonic spasms. The reflexes in the hind limbs are exaggerated, the legs being quickly drawn up, and showing clonic movements. 6.0. The fore limbs have been quiescent for some time ; movements occiuring in the hind limbs only. 5.3. Reflexes still markedly exaggerated (clonus) in the hind limbs, but cannot be elicited from the fore limbs. 5.9. All respiratory movements ceased, and reflexes absent. P. 31. — The chest was opened at once, and slight heart-movements fo\uid to be still present. The bladder, notwithstanding the large quantities of urine ejected during the experiment, was full. The cerebral hemispheres were found to be entirely removed ; the corpora quadrigemina were intact ; the cord was found to be divided within the dura mater at the level of the 5th dorsal vertebra ; the cord was crushed through rather than cut through (scissors, not too sharp, having been used to divide it), but its continuity was completely destroyed. Exp. 153. P.jl, Cat. Weight, 2-4 kilograms. 2. .50. Chloroform anaesthesia induced, and spinal cord exjwsed, and completely divided in the mid-dorsal region ; 1 c.c. of a 0 5-per-cent. solution of tutin was then injected into the peritoneum, and chloroform discontinued. 3.0. No response to electric stimulus applied to left hind foot, but marked response when applied to left fore foot. 3.5. Slight twitching of ears and jerking of head. 3.14., Distinct tutin twitches of head and fore limbs, 3.16, Convulsion of fore part of body, accompanied by movement of tail ; hairs of tail have not become erect ; great salivation. 3.20, Convulsive movement of fore part of body continues ; a movement of the tail near the tip ; 1 c.c, of a 0-5-per-cent. tutin injected into peritoneum, 3.22. Swishing-movement of tail from side to side ; reflex response to pricking left hind leg with a knife distinctly obtained during conATilsion of fore part. 3. 28. Movement of tail during convulsion of fore part, .3.29. Severe convulsions of fore part, accompanied by marked lashing -movement of tail. FiTCHETT. — Physiological Action of Tutin. 357 P.M. 3.32. 3.42. 3.45. 3.46. 3.47. 3.50. 3 52. 3.54. 4.4. 4.5. 4.6. 4.6^. 4.7." More convulsions, with lashing of tail ; movement of tail sometimes occurs quite apart from any movement in fore part of body, but occurs also with marked regularity at the beginning of each fit of fore part. Several movements of tail, with no convulsion of fore part ; tail sometimes moved from root and sometimes only the tip ; movement is mainly from side to side, but now and then the whole tail i s lifted upwards. Reflexes present in the hind part ; movements of both limbs on tapping one. Movement of tail becoming more marked, while fore part more quiescent. Defgpcation occurred. Hind limbs spasmodically dra\vn up to abdomen several times ; then a slight lit of fore part occurred, and movements of tail, with tetanic movement of hind limbs. Tonic and clonic spasm of hind limbs ; claws extruded. Respirations slow and gasping. Heart-beat vigorous ; as heard by stethoscope, 72 per minute. Twitches of fore \rA\\s and tonic spasm of hind limbs, with erection of hairs of tail. Clonic movements of left hind limb. Distinct tonic and clonic spasm of both hind limbs ; limbs fully extended, with claws extruded ; respiration infrequent and difficult, owing to obstruction of air-i)assages by saliva and mucus ; heart intermittent, mis.ses one or two beats towards the end of inspiration. More movements of hind limbs, fore part motionless; respirations about four ])er minute. Another spasm of hind c|uarters. Respirations ceased : heart audible by stethoscope, beating regularly for two minutes and a half after last respiratory gasp. Exp. 154. A frog {Hyla aurea), jjithed in the ordinary way three hours previously, was sus- pended by the head. At intervals of a few minutes its feet (as far as the ankle) were dipped into dilute sulyihuric acid, of a strength of 1 in 1,000. After each dipping the feet were carefully washed in fresh water. The time was taken by a seconds-clock, and the result was as follows : — Fro2 A it Foot. Left Foot 8" 9" 6" 8" 6" 4" 6" 4" 4" 6" 6" 6" 6" 6" 6" 6" Average . . . . . . 6" 6" 6-3 minims of a 0-1-per-cent. solution tutin (11 mlgm. per kilo) was then injected under the skin of the back, and after an interval of 30 minutes the feet were again dipped in the acid : — Right Foot. Left Foot. Frog A .. .. .. ..5" 4" 4" 4" ..6" 6" ..8" 8" Average . . . . 5 '8" 5-5'' Here a further dose of 10 minims was injected, and after an interval of 15 minutes the feet were dipped as before : — Eight Foot. Left Foot. Frog A . . . . . . . . 4" 4" 4" 4" 4" 4" 4" 4" Average . . . . . . 4" 4" Each time the feet were withdrawal together, and, it was thought, more actively tlian before the tutin was injected. 358 Transactions. Exp. 155. The experiment was repeated with a second frog, pithed in the same way four hours previously. The result was as follows : — Bight Foot. Left Foot. Frog B . . . . . . . . 6" 7" ..10" 11" ..8" 8" ..8" 8" ..8" 8" ..8" 8" ..8' 8" ..8" 8" Average .. .. .. 8" 8-3' 10 minims of a 0*l-per-cent. solution tutin was then injected under the skin of the back, and after an interval of half an hour the reaction-time again tested. The time when movement first took place only was noted. Twitched at 2" ; wthdrawn at 4" frog B . . . . . . . . . . . . 6" 6" 6" 14" 14" 20" 16" 22" 14" Average . . . . . . . . . . 12-2" At 22 seconds there was a slight twitch, but no further movement took place, although 70 seconds were counted. Pinching or pricking a foot met with an immediate response, but the acid had no influence. Five minutes later no reflex movement could be elicited by any means, and the heart could no longer be seen beating through the chest- wall. Frog A was then tested again, and foimd to respond as actively as before. Exp. 156. A third frog, pithed one hovir previously, was treated in the same way. FrogC .. .. 10"\ 5" 5" 5" 5" 5 y Right leg only withdrawn. Frog removed from acid as soon as first movement took place. Average . . 6" 2 minims of a 0-5-per-cent. solution was then injected under the skin of the back, and 10 minutes were allowed to elapse before the feet were dipped again. Frog C . . . . . . 6" \ .. sr .. 5" ' 5" Both legs withdrawn. Average 1 minim of a 0'5-per-cent FrogC solution tutin was then injected into the heart. 5" 6" 6" 6" Average FiTCHETT. — Physiological Action of Tutin. 359 Exp. 157. A fourth frog, pithed one hour previously. FrogD 7" 6" 5" „ V Movements of lower limbs onlv. Average 6 6" 6" 6" 6" 6-1" 5 minims of a 0-1 -per the skin of the back, and Frog D cent, solution tutin (10 mlgm. per kilo) was then injected under six minutes later the test reapplied. 2" Very extensive general movements. Arms moved as well. Legs and subsequent movements of arms. Legs, spreading to arms. Legs, arms not moved so vigorously. Both legs only. Legs only, response more sluggish. Legs only. 4" 2" 1" 2" 4" 5" 4" 4" 2" Legs and arms. Average 3" Exp. 158. The experiment was repeated a fifth time. In this case the frog had been pithed in the usual way one hour previously, but it appeared to retain some })ower of voluntary movement, and was so restless that it was suspected that the cerebrum had not been completely destroyed. Extensive general movement followed each application of the acid. Left Foot. Right Foot. FrogE .. .. .. ..2" 2" 4" 4" 3" 4" . . 12" 4" . . 14" 7" .. 11" 8" . . 12" 9" .. 9" 11" 8" 6" Average 8-3" 6-1" 1 minim of a 0-5 per-cent. solution tutin was then injected (about 12 mlgm. per kilo) under the skin of the back, and 15 minutes later the feet were again dipped into the acid ; but before this was done a typical tutin convulsion occurred. Frog G ft Foot. Right Foot. 13" 20" 9" 9" 50" 70 seconds were counted, but the right foot was not withdrawna. 38" 38" 20" 15" Average . . , , . . 22" On examination the optic lobes were found to be intact. 20" 360 Transactions. Exp. 159. The experiment was repeated with a sixth frog. This was beheaded a Httle in front of the anterior border of the tympanic membrane, so as to sever all in front of the top of the medulla. Frog F Right Foot. Left Foot. 7" ii" 7" 1" 9" 9" 8' 9" ..14" 12" .. 15" 13" Average .. .. ..8-5 9-1 1 minim of a 0-5-per-cent. solution was then injected under the skin of the back, and 8 miniites later the test reapplied. Right Foot. Left Foot. Frog F . . . . . . . . 10" 10" -.38" 38" ..84" 84" Average . . . . . . 44" 44" As a result of letting the frog fall on the table, a typical tutin sjjasm, with croaking, occurred here. Seemed to require severe irritation to induce a spasm. A spasm occurred on striking sharply with a glass rod. 250 seconds were counted, but feet not withdrawn. Slight twitches occurred, however, at 58", 71", 86", 94", and 120". 100 seconds more, but no effect. Although the acid had ceased to have any influence, it was still possible to elicit reflex action on painful stimulation — e.g., pinching. Ten minutes later reflexes could not be elicited in any way. The thorax was then opened, and the heart found to be still beating. The auricles were distended. Twitcliing occurred as the cord was being pithed. Exp. 160. A few drops of a solution of tutin were introduced into the right eye of a young rabbit. Within a few minutes there seemed to be a very slight dilatation. In an hour and a c[uarter the right pupil was thought to be slightly the larger by an observer ignorant of which eye had been subjected to the test, but the difference was so very slight, if existing at all, that the result was regarded as doubtful. Exp. 161. Four small drops of a 0-5-per-cent. solution tutin were introduced into the left conjunctival sac of a rabbit. It was observed for 15 minutes, and no change in the size of the pujiil was noted. No hyper£emia of the conjunctiva resulted, nor did the con- junctiva become less sensitive. This rabbit died twenty-four hours later, after exhibiting symi^toms of tutin poisoning. Exp. 162. 2.50. Two droits of a 0-5-per-cent. solution of tutin introduced into the right eye of a cat. 2. 52. No apparent effect. 2.55. No change. 3.0. No change. 3.5. Pupils are the same size, and react equally to light. 3. 10. No effect. 4.0. Pupils equal. Exp. 164. . 3.25. 0-5 c.c. of a 0-5-per-cent. solution of coriamyrtin was instilled into the right eye of a rabbit. 3.30. No ai>parent effect. 3.35. Difficult to say if any effect ; the right eye may possibly be slightly contracted. 3.40. An observer ignorant of which eye had been treated was unable to distinguish any difference between the two pupils. 4,0. Pupils appear equal, and react to light with equal readiness. No appearance of irritation of conjunctiva. FiTCHETT. — Physiological Action of Tutin. 361 P.M. ^^- 1^^- 3.14. Two drops of a 0"5-per-cent. solution of coriamyrtin introduced into the left eye of a cat. 3.16. No change in size of pupil observed. 3.22. No change. 3.30. Pu])ils equal, and react to light with equal readiness. 4.0. Pupils appear to be ec^ual. 4.30. No change. Exp. 166. Rabbit. Weight, 777 grams. Jan. 24. At 4.50 gave 13-2 minims of a 0-1-per-cent. solution tutin (1 mlgm. per kilo), hypodermically. „ 25. No obvious effect. ,, 27. Gave 13-2 minims of a 0-1-per-cent. solution, per os. ., 28. Normal, so gave 13'2 minims of a 0'1-per-cent. solution, per os. ,, 30. Repeated dose of 13-2 minims of a 0'1-per-cent. solution, given jier os. f'eb. 4. Weight, 848 grams. Gave 21-6 minims of a 0-1-per-cent. solution (1-5 mlgm. per kilo), per os. ,, 8. Normal. Gave 4 minims of a 0-5-per-cent. solution tutin (1-5 mlgm. per kilo), per OS. ,, 11. Weight, 879 grams. Gave 2 mlgm. per kilo, per os. ,, 12. No symptoms ; normal. ., 14. Weight, 862 grams. Gave 7-3 minims of a 0"5-per-cent. solution tutin (2-5 mlgm. per kilo), per os. „ 17. Weight, 922 grams. Normal, so gave 7"8 minims of a 0-5-per-cent. solution tutin (2-5 mlgm. per kilo), per os. „ 20. Normal. „ 24. Weight, 958 grams. Normal, so gave 9 "7 minims of a 0-5-per-cent. solution (3 mlgm. per kilo), per os, ,, 27. Weight, 983 grams. Gave 11-6 minims of a 0-5-per-cent. solution (3 mlgm. per kilo), par os. Mar. 3. Weight. 991 grams. Gave 13-4 minims of a 0"5-per-cent. solution (4 mlgm. per kilo), per os. ,, 7. Normal. Gave 5 mlgm. per kilo, per os. ,, 9. Normal. ,, 12. Weight, 1,154 grams. At 2.40 p.m. gave 23-5 minims of a 0"5-per-cent. solution tutui (6 mlgm. per kilo), per os. At 4 p.m. shows symptoms ; extends fore and hind limbs, and lies on belly ; ears and head tremulous. ,, 16. Weight, 1,181 grams. Gave 7 mlgm. per kilo. Not continuously observed. Recovered. ,. 19. Weight, 1,176 grams. Gave 8 mlgm. per kilo. In 3| hours showed symptoms (twitching of ears, chewing-movements, &c.). Recovered. ,, 24. Gave 11-6 mlgm. per kilo, per os. Result, death in two hours. Exp. 167. Jan. 24. Guinea-pig. Weight, 627 grams. P.M. 5.0. Gave 10-2 minims of a 0'1-per-cent. solution of tutin (1 mlgm. per kilo), hypo- dermically, with antiseptic })recautions. 6.30. Convulsive movements of jaw ; animal standing in unnatural attitude. Jan. 25. Apparently normal. ,. 27. Gave 10*2 minims of a 0-1-per-cent. solution tutin (1 mlgm. per kilo), per os. ,. 28. Showed no symptoms ; normal to-day, so repeated dose, 10-2 minims per os. ,, 30. No symptoms ; repeated dose, 10-2 minims, per os. Feb. 4. Weight, 644 grams. At 5.36 p.m. mtended to give 17 minims of a 0-1-per-cent. solution tutin (1-5 mlgm. per kilo), per os, but syringe not set before giving, and so probably less than 17 minims given. Feb. 8. P.M. 5..50. Intended to give 17 minims of a 0-1-per-cent. solution tutin, per os, but 17 minims of a 0-5-])er-cent. solution was given by mistake. Mistake discovered, and 0-5-per-cent. gram chloral-hydrate'given, per rectum, at 6.5 p.m. Immediately on withdrawing nozzle of syringe a few pellets of f^ces were discharged, but very little fluid returned. 362 Transactions. P.M. • 6.20. Is under the influence of chloral, but showing twitches of fore limbs. 7.5. Apparently still under chloral ; is quite limp. • \Y 9.0. Awake, and easily startled ; ears cold, and whole body shivering ; was wrapped in towel. 9.20. Will not remain covered up. Shivering not so marked. 10.0. Same. Feb. 9. A.M. 9.0. Apparently normal, quite warm, breathing is regular. P.M. 2.0. Does not seem to have eaten ; seems dazed. II. 0. Did not try to escape when went to lift it, but resents being handled ; otherwise appears normal. Feb. 10. A.M. 9.0. Seems stiff in the hind quarters ; moans when touched ; has not eaten. Noticed moist condition of uroanal opening. P.M. 2.30. Completely paralysed, and cold in hinder half of body ; breathing thoracic ; eyes kept wide open ; moans when liandled, and showed some convulsive movements of fore limbs and head. 3.0. Found dead. P.M. — Stomach distended with gas ; intestines contain mixed gas and fluid contents ; jieritoneum much injected ; appearance suggestive of general peritonitis. Exp. 168. Feb, 27. Cat. Weight, 2-686 kilograms. P.M. 5.12. Gave 13 minims of a 0-13-per-cent. solution of picrotoxin (0-375 mlgm. per kilo), hyjjodermically. 5.22. Quite normal ; cleaning itself. 5.30. , 5.35. 540' ' '^3'™^- ^o departure from the normal. 6.30. ) Feb. 28. Quite normal. Exp. 169. Mar. 3. j; if. Same cat. Weight, 2-699 grams. Fresh solution of picrotoxin. P.M. 4.0. Gave 6-8 minims of a 0-25-per-cent. solution picrotoxin, freshly prepared (0-375 mlgm. per kilo), hypodermically. 4.16. No symptoms. 4.20. Has defaecated, and swallows occasionally, but seems so well that these may be normal appearances. 5.15. No apparent abnormality. 5.40. Same. Mar. 4. Has displayed no symptoms, and seems jjerfectly well. Exp. 170. Cat. Weight, 2-699 kilograms. This cat previously received 1 mlgm. tutin, and recovered ; will now receive an equimolecular solution of picrotoxin, ||^ x 1 mlgm. picrotoxin = 2-66 mlgm. picrotoxin = 18 minims of a 0-25-per-cent. solution picrotoxin. P.M. 5.20. Gave 18 minims of a 0-25-per-cent. solution of jjicrotoxin. 6.0. No symptoms as yet, beyond occasional swallowing. 6.7. Salivating; mouth open, panting, vomited; vomiting repeated several times; breathing slower after vomiting ; defaecated 6.10. Retching; this a more marked symptom "than with tutin. Animal looks much less disturbed than with tutin at this stage. 6.15. Every now and then spasmodic contraction of diaphragm, suggesting hiccough; looks sleepy. 6.20. Twitching affecting fore paws only ; no face or ear twitching. 6.25. Twitching again, more marked, causing a little spring with fore ]iart of body; is very easily startled- y ■ '^ ^ j~ FiTCHETT. — Physiological Action of Tutin. 363 P.M. 6. 27. Another nioie marked twitch ; sudden spring, with fore arms bowed, giving appearance of trying to cling to the ground ; cat more alarmed and astonished at the twitching than in the case of tutin ; cerebrum seems less affected ; twitches at the slightest noise — e.g., tap of foot on floor, or turning page of note-book. 6.32. Much more marked twitching ; cat stands in unnatural attitude, afraid to move ; every movement causes a sharp spasmodic contraction of muscles ; breathing very rapid. 6.35. General clonic convulsion, lasting a minute and a half ; no tonic stage noticed ; rose immediately seizure had passed ; stands in unnatural attitude, afraid to move ; twitching of eyelids noticed for first time ; seems quite clear mentally. 6.40. Very cautiously assumed a sitting-position, on haunches ; continuous twitching ; looks up at once if spoken to ; twitching has not been so general since the con- vulsion, nor is it so easily excited by stamping the foot ; not so much salivation as with tutin ; watching with interest movements of a rabbit in a cage opposite. 6,50. Twitching only very occasional and slight ; sitting with eyes closed, as if dozing ; breathing normal. 6.55. Twitching more marked again, and is again easily induced by a sudden noise. 7.12. Sitting on haunches, in normal attitude; gives occasional uneasy starts; head drawn back quickly, or to one or other side. 7.22. Still tmtching a little ; eyes half- closed most of the time ; no sign of pain. 7. 33. Came to front of cage, and rubbed itself against wires ; then sat down as before ; is still disturbed by twitchings of fore limbs and head, but it is slighter than it Avas, 7.43. Drowsy, but wakes up with a start. 8.0. Starts are much less frequent, and very slight. 8.22. Apparently asleep, sitting on haunches ; no further twitcliing noticed. 8.30. Same. 9.0. Apparently normal. 9.35. Same. Next day. Quite recovered. Exp. 171. pjyj_ Cat. Weight, 3 kilograms. 4.38. Received 10 minims of an emulsion of coriamyrtin (3 mlgm. or 1 mlgm. per kilo). 4.48. Twitcliing fli-st noticed ; saliva dripping from mouth ; mouth open. 4.50. Vomited ; breathing greatly exaggerated. 4.51. Deffficated. 4.54. Breatliing still rapid ; twitching increases. 4.56. General convulsion, mostly clonic, lasted 30 seconds ; pupils dilate with each twitching. 5.0. Panting hard and twitching constantly. 5.1. General tonic and clonic convulsion, emprosthotonos, almost standing on head; breathing suddenly became normal after convulsion ; then lay with face pressed on floor, breathing heavily ; minor twitching continues. 5.7. Clonic convul.sions, chin bent down on chest, limbs spread-eagle on either side ; stands in an elongated crouching attitude, pressing forehead against floor ; respirations, 160 per minute. 5.8. Clonic convulsions, emprosthotonos, pupils return to normal size in intervals. 5.10. Another convulsion; pupils dilated, as usual. 5.11. I 5 12 ' 5" 14' '" General convulsions ; intervals very short. 5!l6*.j 5.20. During a fit, tail rigidly arched over back ; died in tliis convulsion. Heart in- audible to stethoscope immediately after. P.JI. — Three hours afterwards. Membranes of cord and brain markedly congested ; intestines pale ; heart, right side enlarged, left side contracted ; hjemorrhagic patches in lung ; urinary bladder empty ; gall-bladder moderately full ; uterus contained three foetuses ; pieces of cord and brain fixed in 8 per cent, formal sections, made by paraffiia method. Feb. 11. Exp. 173. P_5i Rabbit. Weight, 1-264 kilograms. 4.47. Gave 0-6 grams of a 1-in-I solution chloral-hydrate, per rectum. Slight loss of the fluid. 4.57. Is amesthetised ; gave 17-1 minims of a 0-5-per-cent. solution of tutin (4 mlgm. per kilo), hypoderlnicallJ^ 364 Transactions. P.M. 6.25. Recovered consciousness ; mai-ked twitching of head and ears ; sitting up. 7-15. Sitting erect on fore paws ; sahvating freely ; convulsive movements of jaws. 7.25 Seizures almost continuous ; placed on a table ; it raises itself by straightening to its fore paws, and pushes its body further and further back, then sinks forward 7.45. apparently exhausted, so that the fore limbs are spread out at right angles to the trunk ; meanwhile jaws are grinding together, and saliva seems to be swallowed ; pujjils moderately dilated, but as daylight nearly gone tliis may be natural. 7.57. As condition continues, gave another rectal dose of 0-6 gram chloral. After getting this it showed the symptoms described by Marshall, of pushing itself back till it actually fell backwards over its tail. The puj^il was dilated, and would not contract when a match was held close to it. 8.7. No cessation of symptoms ; fell over tail again ; interval between seizures varies,. about one minute ; no general con\'ulsion, as is the case when chloral is not given. 8.15. Has been quieter the last few minutes, as if dozing as it sits. 8.30. Lying on side, apparently under chloral ; breathing very shallow ; no twitching. 8.40. Respirations extremely feeble. 8.45. Spontaneous movements ; tried to rise ; raised head, and fell over on the other side. 9.0. No further tutin symj^toms ; moves occasionally, especially if touched. 9.30. Still the same ; has passed urine ; is sitting with nose in a corner of cage, as if dozing ; eyes half-shut ; does not mind being touched or handled ; ears cool. 10.0. Same, but has changed its position several times. 10.40. Moving about more freely ; seems to suifer from ii'ritation of the anus ; is more like normal than it has been since 7 p.m. 10.50. Same ; has jjassed some pellets of fseces and some thin fascal matter ; behave? normally when approached, and seems wide awake ; can use all its limbs. Feb. 12. At 5 p.m. seems normal, except that it is suffering from diarrhosa. ., 13. Found dead in the morning. Exp. 174. P.m. Rabbit. Weight, 1-455 kilograms. 5.45. Gave, per rectum, 0-6 gram chloral -hydrate. 5.55. Gave 13-8 minims of a 0-5-per-cent. solution tutin (3 mlgm. per kilo), hyi^o- dermically. 6.10. Animal apparently fully ansesthetised ; wTapped in a soft towel to maintain temperature. 0.25. Same. 7.5. Dazed and sleepy looking ; no movements other than respiratory ; eyes open. 7.35. Made starting-movements with head, and moved hind limbs ; is still uTapped in towel ; removed towel. 8.0. Has had frequent startings, but is very quiet most of the time. 8.25. Sitting up, apparently dozing ; has been somewhat restless, but no sign of con- vulsion ; covered it up with towel, and noticed that it has passed urine. 8.55. Sitting in a corner of cage, quite awake, but does not seem at ease ; still frequent startings ; breathing slow and deliberate. 0.7. Seems to feel some irritation at anus, possibly from the rectal injection ; put its head down, as if to lick anxis. 9.20. Apparently normal. lO.O. Has been continuously observed, but no sign of convulsions. 11.0. Apparently quite normal ; resists having its ears pulled ; has passed some fseces. 11.30. No further change ; sitting with eyes wide open ; easily startled. Next day. Apparently normal. Exp. 175. P.ji. Rabbit. Weight, 1-534 kilograms. 3.15. Gave 1 c.c. (1 gram) of a solution of chloral-hydrate, per rectum, and 20-8 minims of a 0-5-per-cent. solution tutin, hypodermically (4 mlgm. per kilo). 3.25. Lying on side, under chloral anaesthesia ; respiration, 42 ]}ev minute. 3.45. Still sleepy imder chloral ; breathing the same ; no tutin symptoms. 3.49. Turned over on to tJie other side ; respirations, 40 per minute ; blinks eyes once or twice in succession occasionally. 5.0. Twitching and convulsive movements. 5.15. Same convulsive movements. 6.30. Same, but more feeble. 9.20. Died. \ FiTCHETT. — Physiological Action of Tntin. 365 Exps. 176, 177, 178, 179. Four froths. Weights : A, 27 grams (Exp. 176) ; B, 37-5 grams (Exp. 177) ; C, 28 grams (Exp. 178) ; D, 34-5 grams (Exp. 17!>)- p. M. 6.0. To each frog was given 0-012 gram chloral-hydrate, hypodermically. It was intended to give 0-008 gram chloral-hydrate to frog.s C and D, but by mistake they received the same dose (0-012 gram) as A and B. 6.5. B received 15-3 minims of a O-OS-jier-cent. solution tutin (12m]gm. per kilo), hypodermically ; C received 10-4 minims of a O-05-per-cent. solution tutin (11 mlgra. per kilo), hypoderraic^iliy ; D received 14 minims of a 0-Oo-per-cent. solution tutin (12 mlgm. per kilo), hypodermically. Next day. A is normal, B is dying, C is dead, D is dying. Exp. 180. yjj Rabbit. Weight, 1-4 kilograms. 5 55. Gave 1-5 grams urethane, by stomach-tube. G.20. Apparently under, very sleepy and limp. Gave 4 mlgm. tutin per ld!o, hypo- dermically. 7.30. Symptoms first observed ; they were not present at 7.15 p.m. 8.0. Twitching of ears and head, and starts of fore part of body ; no salivation ; was handled a little roughly in trying to see if salivation present, and went into a typical fit ; it lay on one side, and fit succeeded fit in rapid succession ; move- ments chiefly clonic ; no tonic phase could be detected. 8.30. As fits still continue, and animal seemed doomed, tried about 1 e.e. of a 10-per- cent, sodium-carbonate, per rectum. While giving injection noticed involun- tary urination. 8.45. Sodium-carbonate had produced no obvious effect, so tried chloroform ; ad- ministered it as carefully as possible, ^vith a Skinner's mask ; breathing was shallow and rapid ; under influence of chloroform animal became cjuiet, move- ments of limbs ceased, head moved slowly backwards, and breathing ceased suddenly without the least warning ; the heart could not be felt beating, and artificial respiration had no effect. Exp. 181. Feb. 4. Rabbit was chloroformed, stomach-tube passed ; 0-85 e.c. paraldehj^de (1-2 e.e. p.m. per kilo), dissolved in 10 c.c. water, given. 5.0. Noticed that reflexes had returned. 6.15. Asleep. Feb. 5. Recovered. Exp. 182. p_jj_ Rabbit. Weight, 1-551 kilograms. 4.48. Gave ^^ grain hypodermic tabloid of hyoscine hydrobrom, hypodermically. 5.15. Apparently no effect, so gave a second dose of 5-J„ grain, per os. 6.5. No effect. Next day. Normal. Eeferences to Literature 1. " Life and Voyages of Captain James Cook." By Andrew Kippis, D.D., F.R.S. London : George NeAvnes (Limited) ; 190L P. 179. 2. Lijttelton Times. Vol. i, No. 1, p. 6 ; 11th January, 1851. 3. " On the Toot Plant and Poison of New Zealand." By W. Lauder Lindsay, M.D., F.R.S. Edin. British and Foreign Medico-Chirw- gical Review, No. Ixxi ; Julv, 1865. 4. " Story of New Zealand." By A. S. Thomson, M.D. 1859. 5. Otago Colonist. 25th October, 1861. 6. Otago Daily Times. 15th November, 1862. 7. " Studies on the Chemistry of the New Zealand Flora." By T. F. Easterfield and B. C. Aston. Trans. N.Z. Inst., vol. xxxiii (1900). 8. " Plants of New Zealand." By R. M. Laing, B.Sc, and E. W. Black- well. New Zealand, 1906. P. 228. 366 Transactions. 9. " Art Album^f New Zealand Flora." By Mr. and Mrs. E. H. Featon. London, 1889. Vol. i, p. 104. 10. " On Certain Properties of the Tutu Plant." Bv H. G. Hughes, M.P.S. Trans. N.Z. Inst., vol. iii (1870), p. 237. 11. " On the Physiological Action of Coriaria rusci folia, the Tutu Poison of New Zealand." By W. Ledingham Christie, M.D. NeAv Zealand Medical Journal, July and October, 1890. 12. Trans. N.Z, Inst., vol. ii, p. 399, 13. " Narative of Second Voyage." Vol. iii of General Voyages, p. 245. London, 1821. 14. Annual Report, New Zealand Department of Agriculture, Chemical Division, p. 79. Wellington, 1905. 15. " Sur le Coriamyrtin et ses Derives." By M. J. Riban. " Comptes Rendus," p. 746. Paris, 1866. 16. " Manual of the New Zealand Flora." By T. F. Cheeseman, F.L.S., F.Z.S. Wellington, 1906, P. 105. 17. "' Contributions to New Zealand Botany." By W. Lauder Lindsay, M.D., F,R.8,E., F.L.S. London, 1868. P. 83. 18. George M. Thomson, F.L.S., M.P. Private communication. 19. " On the Botany of the North Island." By W. Colenso. Trans. N.Z. Inst., 1868. 20. " Through Canterbury and Otago with Bishop Harper in 1859-60." By Rev. J. W. Stack. P. 14. Printed at Akaroa Mail Office (no date). 21. " On the Extraction of the Poisonous Principle of the Tutu Plant." By W. Skey. Trans. N.Z. Inst., vol. ii (1869), p. 153. 22. Footnote to paper " On Certain Properties of the Tutu Plant." By H. G. Hughes. Trans. N.Z. Inst., vol. iii (1870), p. 243. 23. " Tutu : Part I." By T, H, Easterfield and B, C. Aston. Wellington, 1900. 24. Note in the Proceedings of the Physiological Societv, " Journal of Physiology," vol. 34, 1906. P. xxix. 25. Phil. Trans. London, 1842. Quoted from " Text-book of Physiology," edited by E. A. Schafer, Vol. i (1898), p. 653. 26. " American Journal of Physiology." Vol. 16 (1906), p. 1. 27. Quoted by C. R. Marshall in " Text-book of Pharmacology and Thera- peutics," edited by W. Hale White. London, 1901. P. 646. 28. Arch. f. Exp. Path. \i. Pharmakol. 30, 1892 (quoted by Schmiedeberg, Grundriss der Pharmakologie, 1906, p. 263). 29. Proc. Roy. Soc, B. 79, p. 503. 30. Grundriss der Pharmakologie, 1906, p. 263. 31. Tutere Wi Repa, M.B. Ch.B. Private communication. 32. " Tutu ; Part II." By T. H. Easterfield, Ph.D., F.C.S., and B. C. Aston, F.C.S. Wellington. 1901. P. 3. 33. W. B. Benham. D.Sc, F.R.S., Professor of Biology, Otago University. Private communication. 34. Crichton Browne. Brit. Med. Journ., vol. i, p. 410. London, 1875. '• On Medicinal Plants." By C. C. Baber. Trans. N.Z. Inst., vol. xix (1886). " On the Ink-plant of New Granada." By Dr. Jamieson. Proc. Linn. Soc. vol. vii, p. 120. " Maori Medical Lore." By W. H. Goldie, M.D. Trans. N.Z, Inst., vol. xxxvii (1904). Stuckey. — Neio Zealand Actinian, Bunodes aureoradiata. 367 \ Art. XXXIV. — Notes on a New Zealand Actinian, Bunodes aureoradiata. By F. G. A. Stuckey, M.A. [Read before the Wellington Philosophical Society, Mrd June, 1908.] The family Bunodidce was established by Gosse for the reception of forms " the surface of whose column is studded with persistent tubercles, and which is not provided with marginal spherules or with jDerforations of the integument." Among other genera it included Tealia and Bunodes. The latter genus included one species, B. coronata, which was provided with acontia,* structures which are now recognised as denoting sagartiad affinities. Among the " Challenger " material Hertwig found a Bunodes (B. minuta) " whose structure approaches that of Sagartia more closely than that of Tealia." Considering, therefore, that Bunodes and Tealia should be widely separated systematically, he placed the genus Bunodes among the sagartiads,t and established the family Tealidw, taking T. crassicornis as its type. He made the presence of a strong endodermal sphincter muscle the leading characteristic of the family, also regarding of importance the presence of a large number of perfect mesenteries, and including forms with both smooth and warty columns. Later| he changed the name of the family, restoring the older name Bunodidce. Referring to Gosse's description of various species of Bunodes, we find the hexamerous condition to be constant, the tentacular formulae beinu 6 + 6 + 12 + 24 = 48, 6 + 6 + 12 + 24 + 24 = 72, or 6+6+12+24 + 48 = 96. Again, in Delage and Herouard the number of mesenteries in Bunodes is stated to be 24 pairs, 12 of them being perfect. Gosse's description of T. crassicornis states the tentacular formula as 5+5+10 + 20 + 40 = 80. Again, Bourne§ gives the mesenterial arrangement of T. crassicornis as follows : 10 pairs complete and apparently primary, ]0 pairs secondary, 20 pairs tertiary. There appears to be reasonable g.ound for thinking that the hexamerous and pentamerous forms should not be associated in the same family. Bourne separates them, and, "provisionally accepting" an ingenious suggestion made by Boveri in his " Development and Phylogeny of Zooantharia," makes Tealiidce one of his families in which the hexamerous arrangement is obscured by precocious development of the secondary and succeeding cycles of mesenteries. In a paper (1901) which I have not seen, but which is referred to by Torrey, II McMurrich unites in a new family, Crihrinidrp, Ehrenberg's genus Cribrina, which he thinks synonymous with Bunodes (Gosse), Bunodactis (Verrill), and Evactis (Verrill). As I do not know his reasons for this change, I propose for the present to retain the older name of the family — namely, Bunodido'. Fam.' BUNODID^. Tentacles digitate ; pedal-disc present, acontia absent ; sphincter strong, circumscribed, endodermal ; numerous perfect mesenteries ; column gene- rally covered with warts. * " Actinologia Britannica," p. 204. § " Treatise on Zoology," ed. Ray Laii- t " Challenger" Rejiort, Zoology, vol. vi. kester. X Supplement to " Challenger" Report. i| Proc. Wash. Ac. So., vol. iv, p. 390. 368 Transactiojis . Genus Bunodes. Bunodidce with tubercles arranged in vertical series. Only the series corresponding to the mesenteries of the 1st cycle run the full length of the column. Marginal spherules on edge of disc. 24 pairs of mesenteries, 12 of them perfect, and all fertile except the directives. Bunodes aureoradiata, n. sp. Specific Character. — Yellow radii in 6 groups of 3. Pedal-disc. — Adherent ; slightly wider than the column ; the edge undulate to correspond with the vertical rows of tubercles. On each undula- tion are 2 or sometimes 3 perforations, through which, when irritated, the animal projects nematocysts torpedo-fashion, and in such a manner as at first sight to suggest feeble acontia. Column. — Cylindrical. In full expansion it is higher than the breadth. The lower half is light or yellowish-brown, upper half greenish-brown. There are 24 vertical rows of tubercles or verrucee : near the bottom of the column these become mere markings ; they increase in size as they ascend the column, culminating in a row of 24 white beads at the bases of the outer cycle of tentacles. The rows of tubercles correspond to the endocoeles of he mesenteries ; they consist of evaginations of the body-wall, and contain ctoderm, mesogloea, and endoderm ; they are perforated, and probably are able to act as suckers. The ectoderm of the column contains numerous nuclei, fairly regularly arranged. Cell outlines are indistinguishable in my preparations, but the nuclei are so arranged as to suggest that they belong to long narrow cells. The mesoglcea consists of fibres imbedded in a struc- tureless vacuolated matrix, in which are also a few other immigrant cells from the ectoderm and the endoderm. There are no nematocysts. The endoderm here, as in all parts of the body, contains symbiotic zooxanthellse, which are present in very large numbers. The circular muscle of the wall does not appear to be regularly developed through the whole length of the wall. Tentacles. — Conical and gently tapering. Pore at tip. Colour bronze- green, like that of the oral disc. The tentacles are very sensitive, and completely and quickly retractile ; they number 48, and are arranged in 4 cycles, the formula being 6 -|- 6 + 12 -t- 24 =^ 48. The ectoderm of the tentacles is thinner than that of the column. The epithelial layer contains numerous nuclei, but no cell-walls are distinguishable. There are numerous nematocysts. The nervous layer of the ectoderm appears as a fibrous net- work, with here and there what are apparently nerve-cells. The longitudinal muscles of the tentacles appear as pleatings of the mesogloea. The meso- gloea is not so distinctly fibrous as that of the column ; it is thin and vacuo- lated. The structure of the endoderm is almost completely obliterated by the great numbers of zooxanthell;^ that are present. A few folds on the ondodermal side of the mesogloea indicate the circular muscles of the tentacles. Sphincter Muscle. — In transverse sections of the upper part of the column the sphincter appears as a ring *ly^ng in the angle formed by the wall of the oral disc. In cross-section it is seen to be well developed, endodermal, and of the circumscribed type, not unlike the sphincter of Cradactis digitata figured by McMurrich.* * ■■ Scientific Results of Explorations by the United States Fish Commission Steamer ' Albatross ' " (Proc. U.S. Nat. Mus., vol. xvi, pi. xxxiii). Tkans. N.Z. Inst., Vol. XL I'L. XVII. "ii| '^^ ^.*«^:^^ ^■' A NEW ZEALAND ACTINI AN. -Stuckey. Fiicc p. 36S. Trans. N.Z. Inst., Vol. XLI. I'l. XVIIl. ANEMONES. — St uckey. Trans. N.Z. Inst., Vol. XLl. Pl. XIX. %f--' ^^.^.J^^ »%%*'-^ ANEMONES. — Stuckey. Trans. N.Z. Inst., Vol. XLl. Pl. XX. ^!J V .y;^- -t ,o; -' 1 ^ '\': 1' A' 3 Tf ANEMONES. — Stuckey. Stuckey.— Ncir Zealand Actinian, Bunodes aureoradiata. 369 Oral Disc. — The ectoderm resembles that of the tentacles. The nuclei are large, and there are fewer nematocysts. The radial or ectodermal muscles are strong, and are carried on deep pleatings of the mesogloea. The mesogloea is i imilar to that of other parts. The endodermal or circular muscles are weaker than the ectodermal. The " mouth " is borne on a prominent peristome surrounded by a broken circle of yellow, from which ■extend 6 groups, each consisting of 3 radiating yellow lines with a shorter yellow line between each 2 groups. These yellow radii correspond to the first 3 cycles of tentacles, the tentacles of the 4th cycle being set opposite to the interspaces. .Esophagus. — The colour is greyish-white. There are 2 siphonoglyphs, with inconspicuous tubercles. The insertions of the mesenteries are shown by white markings. Each side of the cesophagus is thrown into 2 large lobes. Outgrowths of the mesogloea, with corresponding foldings of the •ectodermal lining of the oesophagus, give a much folded appearance, which in cross-sections somewhat resembles an exaggerated starfish. Mesenteries. — There are 24 pairs of mesenteries, of which 12 pairs are perfect, 2 pairs being directives ; they are arranged quite regularly — a pair of imperfect mesenteries in each exocoele of the perfect pairs. Strong retractor muscles are borne on the faces of the mesenteries. On the im- perfect mesenteries they extend from near the body-wall to the inner end of the mesentery. The cells of the endoderm are spindle-shaped. Gonads. — None present in any of the specimens sectioned. Dimensions. — Oral disc 12 mm. wide in a good specimen. Height in full expansion rather more than 12 mm. The longest tentacles are about 8 mm. Locality and Habits. — The only specimens I have seen were procured at Oriental Bay by Professor Kirk. The animal lives between tide-marks, almost completely buried in sand and mud. The presence of the zooxan- thellse probably enables it.to adopt this habit. It lives well in captivity. EXPLANATION OF PLATE XVII. Fig. L Directive mesenteiies (cross-section) ; x 04. Fig. 2. Sphincter muscle (cross-section) ; x 270. 370 Transactio7is. Art, XXXV. — On Tivo Anemones found in the Neighbourhood of Wel- lington— Leiotealia thompsoni and Sagartia albocincta. By F. G. A. Stuckey, M.A. [Read before the Wellington Philosophical Society, 2nd September, 1908.] Leiotealia thompsoni. This anemone was first described by Professor Coughtrey* under the name Actinia thompsoni. Professor Hutton| threw doubts on the cor- rectness of the classification, and Mr. H. FarquharJ suggested that it would form the type of a new family of the Artheadce. The strong endodermal character of the sphincter muscle, however, taken with the smooth body- wall and numerou.s perfect mesenteries, determine its place in the genus- Leiotealia. This genus, which belongs to the family Bunodidce, was erected by Eichard Hertwig, 1882, for the reception of what were practically smooth- walled Tealidce. This is referred to more fully in my account of Bunodes aureoradiata. McMurrich's family Crihrinidce, there mentioned, would con- tain the genus Leiotealia. Torrey§ considers that Leiotealia is equivalent to Efiactis (Verrill), and gives the older name priority. I have, however,, retained Hertwig's name. With the definition of Bunodidce given in the note referred to above I define Leiotealia as follows : " Bunodidce without verrucse or acrorhagi, usually with the mesogloeal folds of the sphincter arranged pinnately, and often with longitudinal furrows in the outer surface of the wall." L. thompsoni is one of the finest anemones found near Wellington, its stout tentacles and bright colours making it a very beautiful object when fully expanded. • Pedal-disc. — Adhesive to rocks and boulders. I have found one speci- men adhering to an ascidian which was itself fixed to a piece of seaweed. When the animal is detached, the pedal-disc is often dilated to a great extent. Its substance is thin, plainly showing the insertions of the mesen- teries. It is rather wider than the column. It presents all the general characteristics of the body-wall, processes of the mesogloea running outward in the manner to be presently described. Column. — Cylindrical in shape. Its height can be varied in a rather marked manner in proportion to the diameter of the oral disc. The colour is white and red in alternate longitudinal lines, which, however, are not generally entire, as stated in Professor Coughtrey's description. The colours are deposited in patches, the red in small irregular spots, the white marks being more or less elliptical. This gives the surface of the column a some- what chequered appearance under a lens of low power. The white markings appear to correspond to the endocoeles, the red to the exocoeles of the mes- enteries. There is a distinct ridge or collar round the top of the column. The colour of preserved specimens completely disappears, when the wall is * Trans. N.Z. Inst., vol. vii. 1874. t Trans. N.Z. Inst., vol. xi, 1878. J Lon. Soc. Journ. Zool., vol. xxvi, p. 528. § Proc. Wash. Ac. Soc, vol. iv, 1902, pp. 391-92. Htuckfa'. — Aiieinoiic^ found in Neighbo2irhoo(l of Wellmgton. 371 seen to be thrown into parallel ridges which lie close together, running round the body of the animal like hoops round a cask. Each of these folds is wrinkled or pleated, the pleats being so close together and so nearly in line as to almost present the appearance of longitudinal ridges. The result is that both in cross-section and in longitudinal section the wall presents the appearance of being covered with numerous papillae, into which the mesogloea runs, often branching or folding in them (Plate XIX, fig. 1). Occasionally the folds grow together and fuse, so that here and there we have in the me- sogloea pits lined with ectoderm (Plate XIX, fig. 2). In cross-sections these appear as more or less circular spaces. The ectoderm peels off in the manner described by McMurrich in his account of Leiotealia badia. It presents the usual histological features. Nuclei are numerous, and crowded towards the outer part, while below this the outlines of the cells form a network. The fibrils of the nervous layer form a more or less continuous line. Nematocysts are present in great quantities, and there is great development of large gland-cells, some of which are lenticular, others pyramidal in shape. The mesogloea presents a wavy appearance, and has a few large scattered cells. Fine processes of the mesogloea project inwards, carrying the circular muscle of the wall. This muscle is not. continuous all round the body, but is in bands, which overlap each other. The actual endoderm of the body-wall is thin, and does not present any unusual features. Tentacles. — These are arranged in three cycles — 10 in the first or inner, 20 in the second, 30 in the third. This arrangement gives the appearance of their being placed in groups of six, thus ; : • Each tentacle is conical in shape, and very stout. All the tentacles are equal in size. In colour they are of a dull white, with a mauve tip. In a few specimens, which, it is worth noting, were all obtained from Island Bay, the mauve tip w^as wanting, and in these cases the longitudinal markings of the body-w^all appear to be entire. One specimen had light-brown tentacles. There is a pore at the tip of each tentacle. The tentacles of the first two cycles communicate with the endocoeles, those of the third cycle with the exocoeles of the mesenteries. There is a strong longitudinal muscle borne on numerous fine branching processes of the mesogloea (Plate XIX, fig. 3). Outside this is the nervous layer in the form of a distinct reticulum. The endodermal or circular muscle of the tentacle is not particularly strong. Sphincter Muscle (Plate XVIII, fig. 2). — This is very strong, and endo- dermal in character. It projects into the coelenterm, and forms a rounded cord, easily seen by the naked eye in a dissection. With a good light behind an expanded specimen the sphincter can be seen through the body-wall. A transverse section of the sphincter presents the same pinnate appearance as that described by McMurrich in the sphincter of L. hadia. The endoderm sur- rounding it is thin. The muscular fibrillar are seen in cross-section as small swellings on the sides of the branching mesogloeal processes. In a longi- tudinal section of the sphincter we see the fibres of the mesogloea running in wavy parallel lines, while beside them are the muscular fil)res with their nuclei cut at various angles. Oral Disc. — The colour is reddish-brov,^n, marked in radiating lines by the insertions of the mesenteries. The mouth is set on a darker-coloured prominent peristome, round which is a depression. There are two siphono- glyphs marked by pink tubercles. The structure of the disc recalls that of the tentacles, except that the nervous and muscular layers are not so well developed. 372 Transactions. (Esophagus. — The colour is a dull white, with brighter lines at the in- sertions of the mesenteries. Bourne* states that the sulcar and sulcular siphonoglyphs do not differ in size and structure, but in my preparations one siphonoglyph appears much deeper than the other. This is a feature that frequently appears in sectioned anemones, and may be the result of treatment. On the other hand, it may mark the position of the sulcular directives, which, being the first pair of directives, and having less to pull against than the second pair, may draw the stomodfeum unduly towards them. In my sections of L. thompsoni the deeper siphonoglyph is curiovisly folded, being bent on itself some six times almost at right angles. The cilia of this siphonoglyph are strong, and stained distinctly with hsema- toxylin. Mesenteries. — There are 30 to 32 pairs, all perfect. Two pairs are di- rectives (Plate XVIII, fig. 1). On all the mesenteries both retractor and parietal muscles are very strong ; indeed, the whole animal is remarkable for its great muscular development. The central fold of the mesenterial trefoil stands well out beyond the lateral folds. Gonads. — These appear in the usual place in the mesenteries. In one of the animals sectioned no ovaries appeared, but the body-cavity contained developing ova and embryos from the 2-chambered to the 12-rayed stage. It is interesting to note that one such embryo had 5 chambers. The young develop between the mesenteries until, at any rate, the 12-rayed stage is reached. They then appear to be ready for an independent existence, as I have found none beyond that stage in the body of the parent. Dimensions. — A good specimen would be as much as 6-7 cm. in height and 4-5 cm. in breadth ; tentacles, 2-5 cm. Locality and Habits. — The species is apparently littoral, being found just above and below low-water mark, attached to the rocks and to loose stones. It is apparently fairly well distributed on the coast of New Zealand, but is not very numerous in any locality. It is more plentiful at Plimmerton than at any other place so far as I know. It has been found at most places along the coast between Plimmerton and Wellington. Professor Coughtrey's specimens were found in Otago Harbour. Sagartia albocincta. This anemone was first described by Professor Huttonf as Gregoria albocincta. Gregoria was one of Gosse's genera of the family Sagartidce. As it was erected for a single specimen, which Gosse himself thought might have been immature, and as no specimen has since been found, recent workers have agreed in dropping the genus. In reclassifying this animal I ha^'e adopted McMurrich's definition of Sagartia^ : " SagartincB with smooth column destitute of verrucas, and with, no special arrangement of the cin- clides ; margin tentaculate ; tentacles concealed in contraction, the sphincter being fairly strong." Pedal-disc. — This only slightly exceeds the breadth of the column, and is about equal to the height. It is strongly adherent, and the animal can hardly be removed without damage. The usual histological structures are present. The three layers are all very thin, the mesogloea especially so. * ■' Treatise on Zoology," ed. Ray Lankester, pt. ii, Anthozoa, p. 38. t Trans. N.Z. Inst., vol. ii, 1878. X Pro.^ U.S. Nat. Mus., vol. xvi, p. 176. Stuckey. — Anemones found in Neighbour} iood of Wellington. 373 Column. — The shape is cylindrical. The colour is deposited in alternating vertical stripes, pink and white, pellucid brown and white, brown and yellow, or green and yellow. The upper part often assumes an orange, the lower a greenish tinge. In full expansion the body-wall is semi-transparent. The wall is pierced by a number of irregularly arranged cinclides, which are easily made out in a fresh specimen. They have thickened margins. The wall is traversed by longitudinal ridges, which appear in cross-sections as papillse-like projections. Neither ectoderm nor endoderm present any departure from the ordinary structure. In sections, especially in longi- tudinal sections, the mesogloea presents numerous spaces, each containing a deeply staining particle. There is a feebly developed circular muscle in the wall. Tentacles. — These are all opaque, white, and rather fine. They are regularly arranged in four cycles, 12+12 + 24-1- 48. They can be wholly retracted, though the favourite position of the animal when not distended is one in w^hich the tentacles are partially withdrawn, the tips forming a white central mass. In shape the tentacles are conical and pointed. They are subequal, the longest being J to | of the full diameter of the disc. The mesogloea and endoderm of the tentacles are thin and the musculature weak. The nervous layer is well developed. Nematocysts are present. Sphincter Muscle (Plate XX. fig. 3). — This is mesogloeal in character, and is represented by a clavate swelling of the mesogloea. The thin end points downwards, and tapers off into the mesogloea of the wall. In the thickened part run anastomosing strands of the supporting layer, forming irregular cavities, in which are seen the muscle-fibres, which here, consequently, are arranged in bundles. Oral Disc. — The disc is bright orange in colour, with radial markings. The mouth is set on a peristome. On the inner side the mesogloea bears short stout processes, giving it a notched appearance. The processes bear the endodermal or circular muscle of the disc. The ectodermal muscle is hardly perceptible. (Esophagus. — The oesophagus is dull white, wdth brighter vertical lines. There are 2 siphonoglyphs, and sections show the oesophagus to be much folded. Th^ mesogloea is thick compared with that of other parts, and has a very striking reticular appearance, which recalls the structure of the sphincter. Mesenteries (Plate XX, fig. 2). — These number 24 pairs, of which 2 pairs are directives. Of these 24 pairs, I take 6 pairs to belong to the first and 6 to the second cycle. These are all perfect, reaching the oesophagus, as also do some of the third cycle of 12 pairs. In addition, there are a few rudi- mentary mesenteries of a fourth cycle just showing. The retractor muscles on the perfect mesenteries are narrow, except on the directives, where they are strong, and placed close up to the oesophagus. Acontia are emitted through the mouth and through the cinclides already mentioned. Some specimens emit the acontia much more reluctantly than others. Gonads. — Only on one of the mesenteries did I see in my preparations any indication of a gonad — in this case an ovary. Dimensions. — Height, 10-12 mm. ; and diameter, 7-10 mm. Habits and Locality. — This anemone is found on rocks, stones, and the roots of seaweed. It is very firmly attached, and can only be removed with difficulty. It opens freely in captivity. It is common in the neigh- bourhood of Wellington, and is also recorded from Lyttelton. Hutton's original specimens were found at Dunedin. 374 Transactions. EXPLANATION OF PLATES XVIII-XX. Plate XVIII. Fig. L Leiotealia thompsoni. Directive mesenteries, parts of four other mesenteries, body-wall, and siphonoglypli. Fig. 2. Leiotealia thompsoni. Cross-section of sphincter muscle. Plate XTX. Fig. L Leiotealia thompsoni. Body-wall, showing the ridges into which the outer surface is thrown (cross-section). Fig. 2. Leiotealia thompsoni. Body-wall, showing the mesoglcea pits lined by ectoderm. Fig. 3. „ Part of tentacle (cross-section). Plate XX. Fig. L Leiotealia thompsoni. Showing embryos developing within the body of tbe parent ; one embryo at the " 2-chambered " stage, the first pair of mesen- teries just developing ; the other advanced to the 12-mesenteried stage. Fig. 2. Sagariia albocincta. Directive mesenteries. Fig. 3. ,, Ci'oss-section of sphincter. Art. XXXVJ. ■ — A Revieiv of the New Zealand Actiniaria known to Science, together with a Description of Twelve Netv Species. By F. G. A. Stuckey, M.A., Wellington. [Bead before the Wellington Philosophical Society, 1th October. 1908.] Introduction. This paper was written under the supervision of Professor H. B. Kirk. M.A., of Victoria College, Wellington, to whom I desire to express my deep sense of gratitude and obligation for instruction in biological method during a three-years course of study, and particularly for his advice and assistance in preparing the present paper. My thanks are also due to Mr. William C. Davis, for instruction in the art of micro-photography ; and to Mr. H. Farquhar, who assisted m-e in the identification of species known to him, and also supplied me with a list of works on the subject. Historical. Considering the richness of the actinian fauna of New Zealand and the attractiveness of the work, it is strange that so few workers have studied this subject. Up to the present date, only three New Zealand workers have published accounts of Actiniaria : 1874 — Coughtrey ; one species. 1878 — Hutton ; nine species (five new ; one previously described in the account of the Dana Exploration Expedition ; two described by Quoy and Gaimard, voy. " Astrolabe " ; and one previously described by Coughtrey). 1 898 — Farcjuhar ; seven new species. The first two writers gave only external characters, but Farquhar described the internal anatomy of one of his species. With the exception of Minyas viridula, all the species so far described are littoral. It is a remarkable fact that there were none of our New Zea- land species in the " Challenger " material. So far as I can ascertain from a careful scrutiny of Hertwig's lists, the expedition took no actinans in Stuckey. — A Revieiv of the New Zealand Actiniaria. 375 New Zealand waters, a circumstance which seems to point to the conclusion that there are in this region no abyssal or pelagic forms. Methods. Killing. — Several methods were used. (1.) Electrocution with a strong current (14 amperes) was tried, but the results were fair only. I am of opinion that this method is not good for histological purposes, on account of the destruction of tissue brought about by electrolysis. (2.) In another method the animals, after being expanded in a minimum of sea-water in small glass vessels, were dropped (vessels and all) into a boiling saturated solution of perchloride of mercury. (3.) The animals were stupefied with magnesium-sulphate in sea- water (Tullberg's method), and then either chloroformed or dropped into boiling perchloride of mercury. The last two methods yielded the best results. Fixing, Imbedding, and Cutting. — All specimens were fixed by immer- sion for a longer or shorter period, according to size, in perchloride of mer- cury. The larger specimens were filled with the fixing fluid through the mouth by means of a glass syringe immediately after death. The mercui'v having been removed with iodine, the specimens were dehydrated in the ordinary way, and finally imbedded in paraffin. Sections were cut with a Cambridge rocking microtome, and, in the case of some of the large species, with a sliding microtome. Staining. — Mass staining with borax-carmine yielded results which were satisfactory, but not so good as those obtained by staining on the cover - slip. Saffranin and methylin blue yielded good results, the nuclei staining well. Fuchsin was found a fine stain for nuclei and nematocysts. Kleinen- berg's hsematoxylin gave good definition of mesogloea. The best results were got with Erlich's hfematoxylin. This was used full strength (Squire's formula), or diluted with water in various proportions. All yielded ex cellent results. After staining on the cover-slip the sections were washed in " tap " water, in some cases being immersed in the water for several days. I am convinced that the best results with this stain are obtained bv using it full strength, and then washing out for four or five days in water. List of Species described. Grade I. PA RAM ERA. Order EDWARDSIIDEA. Genus Edwardsia (Qua tref ages). 1. Edwardsia tricolor (Farquhar), nom. nov, 2. Edwardsia ignota, sp. nov. Grade IJ. CRYPTO PARA MERA. Order ACT INI IDE A. Suborder MALACACTINIiE. Group HEX ACTINIA. Fam. Anthead^. Genus Actinia (Browne). 3. Actinia tenebrosa (Farquhar), 376 Transactions. Genus Anemonia (Risso). 4. Anemonia olivacea (nom. nov.), Hutton. Fam. Sagartidje. Genus Sagartia (Gosse). 5. Sagartia albocincta (nom. nov.), Hutton. 6. „ nutrix (sp. nov.). 7. „ vagrans (sp. nov.). Genus Thoe (Wright). 8. Thoe alhens (sp. nov.). Genus Halcampactis (Farquhar). 9. Halcampactis duhia (sp. nov.). Fam. Paractid^. Genus Paractis (Andres). 10. Paractis feraz (sp. nov.). Genus Tealidium (Hertwig). 11. Tealidium cinctum (sp. nov.). Fam. CORALLIMORPHID^. Genus Corynactis (AUman). 12. Corynactis haddoni (Farquhar). 13. „ gracilis (Farquhar), 14. „ m,ollis (Farquhar). 15. ,, albida (sp. nov.). Fam. Phyllactid^. Genus Cradactis (McMurrich). 16. Cradactis plicatus (Hutton), nom. nov. 17. ,, magna (sp. nov.). Fam. BuxoDiD.^:. Genus Bunodes (Gosse). 18. Bunodes aureoradiata (sp. nov.). 19. Bunodes inconspicua (nom. nov.), Hutton. Genus Leiotealia (Hertwig). 20. Leiotealia thompsoni (nom. nov.), Coughtrey. Fam. Aliciid^. Genus Phlyctenactis (gen. nov.). 21. Phlyctenactis retifera (sp. nov.). 22. ,, morrisonii (sp. nov.). Genus (?). 23. Species (?). Stuckey. — A Review of the Xew Zealand Actiniaria. ^11 To this list I append, for the benefit of other workers, the following list of other New Zealand species which are at present known, but more or less inadequately described. I have not seen any of these species : — 24. Edwardsia neozealanica (Farquhar). 25. Halcampactis mirabilis (Farquhar). 26. Paractis momlifera (Drayton, Milne-Edwards, Hutton). 27. Actinia striata (Quoy and Gaimard, Hutton). 28. Phymactis pohjdactyla (Hutton). 29. Minyas viridula (Quoy and Gaimard, Milne-Edwards, Hutton). 30. Sagartia crocata (Hutton). 31. Peachia carnea (Hutton). General Results. One new genus has been erected and one abandoned genus re-established. Twelve new species have been described, four species have been placed in other genera than those in w^hich they were placed by their original de- scribers, and one species has received a new specific name. For all these changes reasons are given in the text. In general, the anatomy of all species is normal. Actinia tenehrosa shows great variation in the number and arrangement of its mesenteries. The histology of the Actiniaria has been so fully worked out by the Hertwigs that little remains to be said on the subject. The structure of ectoderm and endoderm showed no departure from the normal type, with the exception of the ectodermal pits found in Leiotealia thomfsoni. The mesogloea, however, showed some considerable variation. In the majority of cases it presented the usual features — namely, " a homogeneous matrix in which fibres are imbedded." In other cases lacunae were found to a greater or less extent, especially in the tentacles of Phlyctenactis retifera, where the mesogloea was found to be highly reticular. There are fine sphincter muscles in Leiotealia thompsoni and Cradactis plicatus, more especially in the former. A peculiar arrangement of the " trefoil " of the mesenterial filament was noted in Actinia tenehrosa and Corynactis haddoni. With regard to gonads, it is a common occurrence for observers to fail to find them in their specimens, either because the animals are immature, or because the reproductive cells are found at certain seasons only. In the papers enumerated hereunder, describing British anemones and those collected in various expeditions, out of 163 species described gonads were found in sixty-nine only. Of the twenty-three examined by me, and de- scribed in this paper, gonads were located in nine. In two cases the animals were found to be viviparous : one had ova in brood-pouches ; another was observed to divide in a manner for w^hich I suggest the name " lateral fission." __ Books and Papers referred to in this Paper. Andres, A. " Le Attinie." " Fauna und Flora des Golfes var Naepel." 1883. Bourne, G. C. " Treatise on Zoology." R. Lankester. 1900. Coughtrey, M. " Description of a New Species of Actinia." Trans. N.Z. Inst., vol. vii. 1894. Delage and Herouard. " Traite de Zoologie Concrete." 1901. Dixon, A. F. " Arrangement of Mesenteries in the Genus Sagartia." Proc. Roy. Dub. Soc, vol. vi, n.s., pt. 3. 1888. Dixon, G. Y. " Remarks on Sagartia venusta and Sagartia nivea." Ibid. 378 Transactions. Dixon, A. F. and G. Y. " Notes on Bunodes thallia, Bunodes verrucosa, and Tealia crassicornis.'''' Proc. Roy. Dub. Soc, vol. vi, n.s., pt. 6. 1889. Duerden, J. E. " The Actiniarfan Family Aliciidce." Ann. and Mag. Nat. Hist., 6th series, No. 115. 1897. Farquhar, H. " Preliminary Account of some New Zealand Actinians." Linn. Soc. Journ. Zool., vol. xxvi. 1898. Gosse, P. H. " Actinologia Britannica." 1860. Haddon, A. C. " Revision of the British Actinice,'' Part I. Trans. Roy. Dub. Soc, vol. iv, ser. ii. No. v. 1889. Haddon, A. C, and Shaekleton, A. M. " Revision of the British Actinice" Part II. Trans. Roy. Dub. Soc, vol. iv, ser. ii. No. xii. 1891. Haddon, A. C, and Shaekleton, A. M. " Report on Zoological Collections made in Torres Strait." Trans. Roy. Dub. Soc, vol. iv, ser. ii, No. xiii. 1891. Hertwig, R. " Report on the Actiniaria dredged by H.M.S. " Challenger " during the Years 1873-76." " Challenger "" Report, vol. vi. 1882. Hertwig,R. Supplement to Report, &c. "Challenger" Report, vol. xxvi. 1888. Hickson, S. J. " Cambridge Natural Historv," vol. i. Hutton, F. W. " The Sea Anemones of New Zealand." Trans. N.Z. Inst.. vol. xi. 1878. McMurrich, J. P. " Report on the Actinian Collections made by the U.S. Fish Commission steamer ' Albatross ' during the Winter of 1887-88." Proc. U.S. Nat. Mus., vol. xvi. 1893. Moseley, H. N. " On New Forms of Actiniaria dredged in the Deep Sea." Trans. Linn. Soc. Lond., Zoology, ser. ii, vol. i, pt. 5. 1877. Parker, G. H. " Longitudinal Fission in Metridium margenaUimy Bull. Mus. Har. Coll., vol. xxxv, No. 3. 1899. Torrey, H. B. " Anemones, with Discussion of Variation in Metridium.'''' Proc. Wash. Acad. Sci., vol. iv. 1902. Description of Species. Genus Edwardsia (Qua tref ages). 1. Edwardsia tricolor (nom. nov.), Farquhar, 1898. This species (fig. 1) was described by Farquhar under the name Edwardsia elegans. I have changed the specific name to tricolor, the name elegans having been in use for another species since 1849. Mr. Farquhar has fully described the external appearance of this species, so I shall only briefly state my own obser- vations. The body is brown, wrinkled, and covered with a rough cuticle, which is thin at the upper end. It is marked longitudinally by 8 double brown lines. There is a strong constriction between body and capitulum. The lower part of the capitulum is bulbous, and is divided into 8 segments by double 'white lines, continuous with the brown lines of the C'^v^/ scapus (fig. 2). In colour each segment is brown, with a large white spot. Fig. 1. Above this is a narrower white portion. The tentacles Fig. 2. Stuckey. — A Review of the New Zealand Actiniaria. 379 are in two cycles, 8 in each, those of the outer cycle corresponding to the white lines, those of the inner cycle to the interspaces. The tentacles are transparent, yellowish-brown in colour. Cross-sections show that there are 8 ,,Ol'^"'r fnoloderm -^\S Mesoff/oe a rct0^.rrr,WMm \\M\^ — £ndocJerm ^^^Sr — Mesoj/v % '«-«c3t^-'' ^ "•■ \^ ^ V ,. - \ ■ ■ N REVIEW OF NEW ZEALAND ACTINIARIA.— Stuckey. Tkans. N.Z. Inst., Vol. XLI. Pl. XXV. \ !' REVIEW OF NEW ZEALAND ACTIN lARIA.— Stuckey. Trans. N.Z. Inst., Vol. XLI. Pl. XXVI. J REVIEW OF NEW ZEALAND ACTINIARIA. — Stuckey. Trans. N.Z. Inst., Vol XLT. Pl. XXVII. REVIEW OF NEW ZEALAND ACTINIARIA.— Stuckey. Trans. N.Z. Inst., Vol. XLI. Pl. XXVIII. %% /• ^. ^t-a« % REVIEW OF NEW ZEALAND ACTINIARI A.— Stuckey. Stuckey.^ — A Review of the New Zealand Actiniaria. 385 by the following species : sphyrodeta, pallida, piira — to which will be added most of the species which I defer to the appendix. These have no con- spicuous suckers, discharge acontia less and less abundantly, are in general destitute of positive colour, and have a tendency to a colourless trans- parency. . . . Should a generic name ever be required for this group I propose for it that of T^oe." (I have above ascribed the name Thoe to Wright, and it would appear that this is correct, since he described the genus in 1858, while the date of the " Actinologia Britannica " is 1860. It should be noted, however, that that work was published in parts, the publication extending from March, 1858, to January, 1860.) Sphyrodeta has a smooth column ; substance pulpy — features which it possesses in common with pallida and pura. Sphyrodeta and pallida each have rings of colour round the bases of the tentacles ; pura has the bases of the tentacles more opaquely white than the rest of the body. On Lessnnia at Island Bay occurs a small sagartiad anemone which strikingly exhibits features in common with the species above named. The discovery of this form has induced me to re-establish Wright's genus by accepting Gosse's suggestion. The genus would contain the following species : — Thoe sphyrodeta (A. Candida, Gosse, 1853 ; S. sphyrodeta, Gosse, 1858 ; A. Candida, Tag well, 1856 ; T. sphyrodeta, Wright, 1858 ; S. sphyrodeta, Gosse, 1860). Thoe pura {A. pellucida, Alder, 1857 ; S. pelhicida, Gosse, 1858 ; T. pura, Wright, 1858 ; S. pura, Gosse, 1860). Thoe pallida {A. pallida, Holdsworth, 1855, and Milne-Edwards, 1857 ; .S. pallida, Gosse, 1858, 1860). Thoe alhens, sp. nov. And also, with less certainty, the five species enumerated by Gosse (Act. Brit. p. 354) : ahleri (Cocks), pellucida (Cocks), yarrcllii (Cocks), bellii (Cocks), and hastata (Wright). The genus will be defined thus : " Sagartincn without conspicuous suckers ; cinclides absent, or visible only on the discharge of acontia ; body- wall smooth or with inconspicuous suckers ; acontia discharged reluctantly ; generally without positive colour or with only local deposits of pigment ; substance of body pulpy." 8. Thoe albens (sp. nov.). This species in expansion is opaque-white, but is so pulpy that in con- traction it looks Hke a small shapeless mass of transparent jelly. This makes it difficult to kill well, and extremely difficult to riake good histo- logical preparations of the animal. Pedal-disc. — Adherent to Lessonia, below low-water mark. The ecto- derm and endoderm are thicker than the mesogloea. The latter shows the fibrous structure characteristic of most actinians. It also contains a num- ber of lacunae. The nerve-layer of the ectoderm is very well developed. The disc spreads out a little beyond the column, the outspread portion being marked with golden-yellow radial lines. Column. — Similar in structure to the pedal-disc, but thinner. It has the appearance of having a mesogloeal circular muscle throughout its whole height. It is smooth, with no suckers or verrucse. Neither are there any 13— Trans. 386 Transactions. visible cinclides except when the acontia are ejected. The colour is white. Sphincter Muscle. — There is a spindle-shaped thickening of the meso- gloea in the upper part of the column, causing a slight bulging of the wall. In the sphincter the muscle spaces are very close together, but otherwise this muscle is of the usual sagartian type. Tentacles.— There are 96, in four cycles, 12 + 12 + 24 + 48 = 96. In colour they are opaque-white, like the column ; in shape, conical and tapering. The length is rather more than half the diameter of the disc. At the base of each tentacle is an incomplete ring of yellow pigment, the open part directed inwards and the outer circumferences of / \ the rings close together, so as to make an almost continuous ^ (§)(§) I'i^g ^^ yellow round the top of the column under the ten- tacles (fig. 7). Nematocysts are numerous in the tentacles. Fig. 7. 'pj^g ectoderm and endoderm are relatively thick, the me- sogloea being reduced to a mere streak. The muscle-bearing processes on both sides are few in number. The nerve-layer is compact, and appears almost as a line in cross-sections. There are numerous large irregular spaces in the ectoderm. Oral Disc. — Colour white, as in the tentacles and column. Mout'j is set on a peristome. The stomodseum is white, and there are 2 siphono- Mesenteries. — Owing to the difficulty of killing and fixing this species I was unable to determine accurately the number and arrangement of the mesenteries. Acontia. — These are emitted reluctantly, some through the mouth, others from cinclides which are placed on the column just under the yellow line at the bases of the tentacles. The acontia are long, and con- tain very large numbers of nematocysts, together with many nerve-cells. The processes of the nerve-cells run between the closely packed nematocysts (fig. 8). Habits. — This species lives in the chinks among the -piG. 8. " roots " of Lessonia. It is impatient of light. Dimensions. — In full expansion it is 12 mm. high and 10 mm. in dia- meter. The pedal-disc is rather wider than the column. Distribution. — Of the genus — British Isles, New Zealand. Of the species — Island Bay. Genus Halcampactis (Farquhar). This genus, which I consider to be closely allied to Ch and r actinia or to Paraphellia, will probably become the type for a new subfamily of sagartiads. By its author it is ascribed to the family Halcam/pidw. At the same time he considers it as constituting a link between that family and the Sagartidce. I have not been able to find Farquhar's Halcampactis mirahilis, though I made one search in company with Mr. Farquhar, and have been out several times myself and with Professor Kirk, the original discoverer of the animal. I have, however, seen the original sections of H. ■mirabilis, but until I have been able to rediscover the species described by Farquhar I prefer to simply place the genus provisionally in the Sagartidce. While searching for Hal- campactis mirabilis I found three specimens of the species to be now described, a species which probably belongs to the same genus. Stuckey. — .4 Review of the New Zealand Actiniaria. 387 9. Halcampactis dubia (sp. nov.). The body is pink in colour and vermiform in shape. The epidermis is smooth, with very minute papillfe on the upper portion. The body is divisible into capitulum, scapus, and physa, the division between the last two being slight. A red line marks the division between scapus and capitu- lum. The capitulum, which is capable of being entirely invected, bears 24 pink tentacles, in two cycles. The scapus is marked by 6 double longi- tudinal white lines. The physa is adherent and flattened. It is thin, the filaments and acontia being plainly visible through it. The animal does not emit the acontia, but if a slit be made in the body they stream out readily. They are of the usual character, and the nematocysts are closely packed. T have not yet worked out the anatomy and histology of this species. Dimensions. — The largest specimen was 25 mm. long and about 3 mm. in diameter. Distrilndion. — Of the genus — The coast near Wellington. Of the species — Island Bay. Fam. PARACTID.E. I adopt Hertwig's definition as modified by McMurrich : " Actinice usually with numerous perfect mesenteries ; circular muscle strong, im- bedded in the mesoaloea ; acontia wanting." Genus Paractis (Andres). " Paractidre with smooth body-wall, without papillae or marginal spher- ules ; tentacles slender, and not exceptionally numerous ; nearly equal in length and strength ; margin not lobed ; sphincter widening somewhat abruptly in its upper part, and occupying, near the margin, nearly the entire thickness of the mesogloea." 10. Paracti,s ferax (sp. nov.). Pedal-disc. — Adherent to the under-sides of stones, or to rocks, in dark places. The chief histological feature is the thick mesogla?a, which is indeed a noticeable feature of the whole animal. The fibres are wavy, and there are many lacuna^. The ectoderm is of the usual type, about half as thick as the mesogloea. The endoderm is thin. Column. — It is generally cylindrical in shape, but is occasionally con- stricted at various parts, giving the animal a vase-shaped contour. The column bears, especially in contraction, fine transverse wrinkles. Its height can be varied very considerably, but is generally equal to two or three times the diameter. The colour is ^ milky white. In contraction the ani- mal is drawn into a hard rounded ball of the size of a small marble. The ectoderm and endoderm are of the normal type. The mesogloea is thick, about equal to the ectoderm, but at intervals it be- comes thin, as shown in fig. 9. This feature seems to be characteristic. In other places, numerous enough for the yig 10 structure to be considered characteristic, the mesogtoa forks, sending out a process which is lined on both sides by ectoderm, and which Hes close to the body-wall (fig. 10). 388 Transactions. Tentacles. — These are conical in form, tapering to a fine point, and reduc- ible to thin filaments. In colour they are white, with brown markings. Each has a brown tip. They are arranged very evenly in four cycles, the inner two nearly equal. Each of these two contains 6 tentacles ; the third contains 12 slightly shorter ; the fourth contains 24, shorter still. The ectodermal muscles are strong, and are borne on long processes of the mesogloea. The mesogloea is very fibrous, and contains a large number of nuclei. There are numerous nematocysts. Oral Disc. — The disc is white, mth a sUght brownish tinge. Some specimens have radiating brownish lines. There is a pair of opaque-white lines radiating from the siphonoglyphs to the edge of the disc. The mouth is some- what depressed, and the siphonoglyphs are not prominent. The stomodaeum is not readily everted. The histological characters of the disc closely resemble those of the tentacles. Sphincter Mxiscle. — This is mesogloeal in character, consisting of a thickening of the mesogloea in the upper part of the column, the thickened portion containing numerous muscle-spaces. The whole mesogloea of the wall is muscular, producing, no doubt, the strong contraction which is so characteristic of the animal. Mesenteries. — There are 32 to 36 pairs, 2 pairs being directives. The musculature is very strong, the muscle-banners appear- ing as great rounded masses, but slightly attached to the mesentery (fig. 11). Gonads. — The mesenteries are all fertile, except the directives. All the animals sectioned happened to be females, and all showed remarkable fertility. Ova appeared at nearly all stages. At first they occupy a position imbedded in the mesogloea (fig. 11). but as they advance in maturity they form ereat masses, almost filling the intermesen- terial spaces (Plate XXIV. fig. 1). Finally they may become detached ^ii>^ from the mesenteries and form globular masses, showing in cross - sections as rounded discs (Plate XXVjI-). bryos were seen. Habits. — All my speci- mens were found in dark Fig- 11- places, never more than four in one place, usually single specim ns. The species seems rather uncommon. Dimensions. — .2-18 mm. in diameter, 25-45 mm. in height. or rings No em- Stuckey. — A Review of the New Zealand Actiniaria. 389 Distribution. — Of the genus — Mediterranean, Red Sea, Indian Ocean, Atlantic, Tierra del Fuego, New Zealand, Pacific, China Sea. Of the species — Island Bay, Ohiro Bay. Genus Tealidium (Hertwig). ParactidcB having the tentacles placed in several rows of uniform size in the same row, and having the body-wall covered with fine papilla?. All mesenteries perfect and gonophoric except the directives. (Hertwig's definition modified.) This genus was erected by Hertwig for the reception of a form found in the " Challenger " material, a form which agreed with Paractis except in the warty character of the body- wall. In Hertwig's species (Tealidium cingulatum) the wall bulges outwards, forming a girdle below the tentacles. This he attributes to the great development of the sphincter. In the species described below the same thing is seen, though I have no direct evidence that it arises from the cause ascribed by Hertwig. Probably this feature may come to be regarded as of generic value. 11. Tealidium cinctum (sp. nov.). • Pedal-disc. — Adherent in cleft of rock, making the animal difficult to remove. The mesoglcea is fibrous, and contains numerous lacuna?. Column. — The upper part is brownish in colour, the lower part dirty- white. The upper part is covered with verrucae in vertical rows ; small shells, &c., are attached to these verrucse. The lower part, which is im- bedded in a cleft of the rock, is without the verruca>, and is channelled by fine furrows. The verrucse act as suckers, by which the animal covers itself with bits of shell and other debris. In full expansion the column bulges outwards, forming a circular swelling just under the bases of the tentacles. The ectoderm is somewhat irregular, and there appear here and there spaces between the cells. The nerve-layer is feebly developed. The mesoglcea is well developed, and contains small lacunae. It runs into the ectoderm in the form of conical papillae. Tentacles. — These are 48 in number, apparently in four cycles. Length, about 16 mm. They are pellucid, with a mauve-pink shade. There are white transverse markings on the inner sides. The ectoderm is of the same irregular character as that of the column, but the intercellular spaces are smaller. The nervous layer is well developed, being several cells deep. There is a fair development of the ectodermal muscles, but the endodermal musculature is w^eak. The lumen of each tentacle is filled with what appears to be hypertrophied endoderm. Oral Disc. — The colour is pale brown, with a ring of green round the mouth, and a broken ring of yellow round the green. The histological features resemble those of the tentacles. Sphincter Muscle. — This is mesogloeal and diffuse, extending through the whole wall of the column. There is, however, a decided thickening under the edge of the disc, and this probably constitutes the true sphincter. Hertwig describes a similar sphincter in Antholoba reticulata. Mesenteries. — There are 24 pairs, 2 pairs being directives. All reach the stomodaeum, and are about equal in development. All are gonophoric except the directives. I have made this a generic feature, since Tealidium cingulatum (Hertwig), the only other known species, has all its mesenteries perfect and gonophoric (? directives). The musculature is well developed. (Plate XXIV, fig. 2.) 390 Transactions. Gonads. — Placed much, as in Paractis ferax, and form large masses between the mesenteries. Dimensions. — Height, 40 mm. ; diameter, 30 mm. Distribution. — Of the genus — Antarctic Ocean (Delage and Herouard) ; also New Zealand. Of the species — Island Bay. Fam. CORALLIMORPHIDiE. " Hexamerous Actinice with a double corona of tentacles, a corona of marginal principal tentacles, and a corona of intermediate accessory tentacles. Mesenteries slightly differentiated and all gonophoric. Muscular system weak in all parts of the body. No sphincter." Genus Corynactis (Allman). The tentacles are all knobbed. They are arranged in radial series, so that more than one communicate with each inter- or intra-raesenterial space. Farquhar described three species of Corynactis from the neighbourhood of Wellington. These are C. haddoni (with seven varieties), C. ■mollis, and C. gracilis. In external form these species are all very similar, their chief apparent difference being in the matter of colour. I think it not unlikely that the species and varieties enumerated by Farquhar may prove on investigation to belong to only one species. I have not yet, however, been able to collect specimens of all the species of C. haddoni, and have therefore to defer the investigation. To the species mentioned above I add a fourth, C. albida. In external appearance this corresponds closely to C. haddoni, except in colour, which is pure white, without any deposit of pigment. The principal tentacles are very long and slender, inclining slightly outwards in expansion. The accessory tentacles stand upright. Farquhar has so carefully described the external appearance of his species that there is no need for repetition here. I have not yet fully worked out their anatomy and histology, but have made the following notes : — 12. Corynactis haddoni (Farquhar). 13. ,, gracilis (Farquhar). 14. ,, mollis (Farquhar). 15. ,, albida (sp. nov.). Mesenteries. — In all four species there are 24 pairs, of which 12 pairs appear, typically, to be perfect. There is scarcely any indication of retractor muscles in any species, but the parietal muscles are generally fairly well developed. On the filaments in some sections I noticed the same appearance of three trefoils as I have described in Actinia tenehrosa. Sphincter Muscle. — On account of the complete infolding of the tentacles Farquhar supposes the sphincter to be well developed, and in this belief he is supported by Delage and Herouard. A large number of longitudinal sections of the four species under survey failed, however, to show the slightest indication of a sphincter. C. haddoni : Though there is no sphincter, there is a fairly distinct circular muscle in the wall. This consists of a few fibres running on the endodermal side of the mesogloea. The mesogloea is homogeneous. The ectoderm is the thickest of the three layers, the other two each being about half its thickness. Stuckey. — A Review of the New Zealand Actiniaria. 391 C. gracilis : The mesogloea of the column contains a single row of spaces, more or less round. This feature, however, may prove to be the result of treatment. C. mollis : The mesogloea is very slightly fibrous. The stomodaeum is much folded, and into it run processes of the mesogloea. The musculature of the mesenteries is stronger than that of the other species. C. albida : As in C. mollis, the stomodfeum is much folded, and has mesoglceal processes projecting into its ectoderm. Each of these processes is opposite to the attachment of a pair of mesenteries. The outer parts of the mesenterial spaces are filled with hypertrophied endoderm. Reproduction. — No gonads appeared in any of my sections, but masses of ova and young animals appeared in the bowl with the animal that divided in the manner to be described below. This was a specimen of C. haddoni taken on the 31st August, 1908. It was on a small stone, and attracted attention on account of the fact that it had spread itself out in the form of a flattened elliptical disc, the length of which was four or five times the diameter of an ordinary specimen, while the breadth was half the length. It was so flattened that the oral and pedal discs were almost in contact. The mouth gaped wide, having been stretched in the same way as the body. © © VII Fig. 12. The mesenterial filaments were plainly visible. The tentacles were almost completely retracted, only the knobs showing. The animal, on its stone, was placed in an aquarium, and closely watched. In two or three days the wall became thin at one extremity of the minor axis of the ellipse, finally splitting at that point. The free ends began to retreat, as it were, in a direction parallel to the major axis. As they approached the vertices of the ellipse they began to curl inwards. A second split occurred about the place marked x in the diagram, and the first daughter organism became free. The two ends gradually curled round, and finally coalesced. In the meantime the last-freed ends began to curl inwards, and another split began to form at the place marked y. The second and third daughter organisms closed up as the first had done. Thus three organisms were formed by a process of fission, which I have called " lateral fission." The whole process, 392 Trai inactions. to the complete formation of the last daughter organism, occupied about seven weeks. In addition to this, a bud appeared, at an early stage, on the foot of what became the last-formed organism. This bud increased in size, and a constriction began to be formed, cutting it off from the parent. This illustrates the process of pedal gemmation mentioned by Farquhar. The method of asexual reproduction which I have called " lateral fission " appears to be different from any of those described in the " Cambridge Natural History," and it also appears to differ from the method called by Delage and Herouard (p. 476) " scissiparite longitudinale." It is an interest- ing fact that during the process of fission ova were released and developed into embryos about \ mm. in height. This nascent colony would doubtless have yielded interesting results, but it was unfortunately destroyed through the neglect of a laboratory attendant, who allowed the water to be polluted by dead molluscs. The drawings illustrating the process described above are only diagrammatic " ground-plans," as it were. (Fig. 12.) Fam. PHYLLACTID.^. " Hexactinice with simple conical tentacles at some distance from the apparent margin ; between them and the margin are low tentacu^lar or foliose structures (fronds). Sphincter endodermal, more or less circu.mscribed, lying in the interval between the tentacles and the frondose or tentacular structures. From two to several cycles of mesenteries perfect." Genus Cradactis (McMurrich). " Ph/IlactidcB with, the fronds represented by bunches of simple or slightly branched, short, tentacle-like structures. Sphincter aggregated or circum- scribed. Column with verrucse." 16. Cradactis plicatus (nom. nov.), Hutton. This anemone was first described by Hutton as Oulactis plicatus. He described the margin of the disc, when expanded, as " thrown into five deep folds." Though I have observed raany specimens, both in their natural home and in an aquarium, I have been unable to observe this feature. At the same time, I have no doubt as to the identity of the species. Hutton placed this anemone in the genus Oulactis, but I have been led by the character of its fronds to place it in McMurrich's genus Cradactis. Pedal-disc. — Adherent and somewhat thin, the insertions of the mesen- teries being plainly visible through its substance. AVhen removed from the rocks the " flange " round the base becomes very noticeable. The ectoderm is comparatively thick, and is curiously strengthened by strands of mesoglcea which in places appear to have lost their connection with the main part of the mesogloea. These strands are not fibrous like the rest of the mesogloea, in which the fibrous structure is particularly noticeable. Column. — This is cylindrical, generally wider than high, and with only a slightly expanded lower portion. Verrucse are present, arranged in vertical rows. They are absent on the lower part of the column. The upper ver- ruc3e act as suckers, by means of which the animal covers itself with stones and shells, so that, when retracted, it resembles a small pile of stones. The colour of the column is yellowish-brown, passing into dirty v/hite below. The mesogloea is prolonged into the ectoderm in pinnate processes. These are arranged in regular vertical rows corresponding to the verrucse. Tentacles and Fronds. — The simple tentacles are conical, and are more than the radius of the disc in length when the whole animal is fully expanded. Stuckey. — A Revieiv of the New Zealand Actiniaria. 393 Their colour is pellucid pale brown, like the colour of thin shavings of horn. They are barred with white on the oral aspect. At the bases of the tentacles, and sending points between them, is a zigzag circle of yellow, with a sug- gestion of pink. The ectodermal and endodermal muscles are both well developed, more especially the former. The nervous layer and the epi- thelial layer are both thick. Outside the simple tentacles, and just on the edge of the disc, is a single row of " compound " tentacles or " fronds," 48 in number, structures which McMurrich regards as differentiated acror- hagi. These are white in colour and multilobed, each often having as many as twenty lobes. They form a wide frill round the animal, giving it a fine appearance when fully expanded. One of the lobes of each frond is con- stantly pigmented with a pink spot or knob. The lobes of the fronds are able to act as suckers. They are not sensitive to tactile stimuli. All the elements of the body-wall enter into the composition of the fronds, except the nervous layer of the ectoderm. Oral Disc. — The margin is raised, as is also the peristome, giving the disc a concave form. The colour varies, yellow, crimson, and deep velvety brown being the chief varieties. The edge of the mouth is generally lighter in colour than the rest of the disc, and is ringed by a deposit of pigment. There are also radiating lines of an orange colour, and there is a broken circle of yellow round the bases of the tentacles, as already mentioned. There are well-developed ectodermal muscles, but the endodermal muscles are weak. On the under-side of the disc — that is, the roof of the coelenteron — are spaces each of which encloses a developing ovum. These spaces are apparently brood-pouches. Sphincter Muscle. — This is endodermal and circumscribed. In cross- section it is heart-shaped. It is placed under the fronds. (Plate XXV, %. 1.) StomodcBum. — There are 2 prominent siphonoglyphs, each marked ex- ternally by a yellow tubercle with a pink top. The stomodfeum is grey in colour, and shows the edges of the mesenteries. Cross-sections of the animal show the siphonoglyphs to be deep and narrow. In addition, the stomo- dseum is folded into 10 other grooves. The ectoderm is provided with a large number of gland-cells. Mesenteries. — There are 48 pairs, two of them directives ; twelve pairs reach the stomodseum. The muscles are strong, the " banners " occupying the larger part of the mesentery. There is strong development of parietal muscles. (Plate XXV, tig. 2.) Gonads. — In one specimen testes were seen on the imperfect mesenteries. In another, ova were found, as described, in brood-pouches. These were the only cases in which I saw sex-cells. Habits, &c. — The animal adheres strongly, the lower part of the column often being placed in a chink of the rock. Its colour is protective, and, in addition, its habit of covering itself with bits of stone and shell helps to conceal it. The concave disc, also, is often covered with sand, so that nothing shows but the mouth and tentacles. Dimensions. — Variable. The largest specimens are 6 cm. in diameter and rather less in height. Distribution. — Of the genus — Delage and Herouard give " Cape Horn," but this does not agree with McMurrich, who locates his species in the Ber- mudas and " Station 2766, lat. 36° 47' S., long. 56° 23' W.," that is just south of the Kio de la Plata. Of the species — Dunedin, Cook Strait. 394 Transactions. 17. Cradactis magna (sp. nov.). I have not seen this species alive. I give the following notes of the gross dissection of a preserved specimen : The base is adherent. The column has about 100 rows of verrucae. The ectoderm is thick, and peels off readily. Not only does the animal attach pieces of shell to itself, but these even become imbedded in the ectoderm. At the oral end of the column is a ring of foliose structures. The tentacles and disc are strongly infolded, suggesting the presence of a powerful sphincter. The mesoglo?a throughout the animal is thick and strong. The tentacles are very nume- rous, and apparently in four rows ; each has a pore at the tip. There are 96 pairs of mesenteries, the first and second cycles being perfect, and each apparently consisting of 12 pairs ; 2 pairs are directives ; all appear normally to be fertile. In contraction the animal is 7 cm. high and 5 cm. broad. Its size when expanded could not be less than 10 cm. in height, and not much less in diameter. This species is found at Plimmerton. Since the above notes \vere prepared I have seen four specimens alive. The column varies in colour, being respectively brownish-yellow, pinkish- yellow, yellowish-green, and pale green in the four individuals respectively. The disc is radially marked with brown streaks, with regular white patches between. The tentacles are short, and arranged in four cycles. They are bicoloured, being in three of the specimens deep purple at the proximal end, bright claret at the distal end. In the fourth the colours were orange and yellow. The number of lobes in the fronds is great ; they are dull grey in colour, not so prominent as the same structures in C. plicatus. The pink spot of C. plicatus seems to be represented here by a white one. The ver- ruese are somewhat cylindrical. The stomodseum is white. There are 2 siphonoglyphs. Fam. BUNODID^. Genus Bunodes (Gosse). 18. Bunodes aureoradiata (sp. nov.). This is fully described in this volume at p. 368. Distribution. — Of the genus — Norway, English Channel, Atlantic, Medi- terranean, Bahamas, Indian Ocean (Delage and Herouard) ; also New Zea- land. Of the species — Wellington Harbour. 19. Bunodes inconspicua (nom. nov.), Hutton. This species was named, by Hutton, Phymactis inconspicua. The ver- tical arrangement of its verructe, however, gives it a place in the genus Bunodes. Basal Disc. — Adherent, rather wider than the column. The ectoderm is twice as thick as the mesogloea. The latter contains lacunae. Column. — Cylindrical, slightly widening towards the base. Verrucse m vertical rows, long and short rows alternating. Towards the lower end of the column they become less numerous and smaller, at last becoming mere marks. The colour of the column is whitish below, olive-brown above. The column closely resembles that of Bunodes aureoradiata. The ectoderm and endoderm are normal, the latter containing zooxanthella?. The mesogloea runs out into the ectoderm, taking part in the constitution of the verrucse. Under the tentacles is a ring of white tubercles or " mar- ginal beads," each one being placed at the top of a vertical row of warts. Tentacles. — These are placed in four cycles, and are about 120 in number. The largest is equal in length to the diameter of the disc. They are conical. Stuckey. — A Review of the New Zealand Actiniaria. 395 and taper to a fine point. In colour tliey are olive-brown, with from 2 to 6 white spots on the inner side. They are completely retractile, and very sensitive. The nerve-layer is distinct, and the ectodermal muscles are strong. The endomermal muscles are weak. The lumen is tilled with zooxanthellfe. Oral Disc. — Flat ; peristome raised. Colour olive-brown. Stomodteum white, often everted. The histological features resemble those of the tentacles. Sphincter Muscle.- — Endodermal. Closely resembles that of B. aureo- radiata. Mesenteries. — Closely resemble those of B. aureoradiata. Gonads. — I saw none in my preparations. Dimensions. — My largest specimens were 15 mm. high, and about the same in diameter, but I am told they grow much larger. Distribution. — Of the genus — -As above. Of the species — Dunedin, Wellington. Genus Leiotealia (Hertwig). 20. Leiotealia thompsoni (nom. nov.), Coughtrey. This species is described in this volume in a separate paper. Distribution. — Of the genus — Magellan Strait, Chili, Kerguelen Island, Arctic Ocean (Delage and Herouard) ; also New Zealand. Of the species — Dunedin (Coughtrey) ; Cook Strait, from Plimmerton to Seatoun. Fam. ALICIIDiE. " Hexactinice with large, flat, contractile base. Tentacles simple, sub- ulate, entacmseous. Column with simple or compound hollow outgrowths or vesicles over more or less of its surface, arranged mostly in vertical rows. No cinclides. Sphincter muscle endodermal and diffuse, variable in amount of development. Perfect mesenteries few or numerous. No acontia." (Duerden.) Up to the present time this family contains four genera — Alicia, Cijstiactis, Bunodeopsis, and Thaumactis. I have several specimens of a form taken at Island Bay and one specimen taken at Stewart Island. Both these forms certainly belong to the Aliciidce, but do not seem to be referable to any one of the hitherto recognised genera. They differ from Alicia in their larger number of perfect mesenteries ; from Cijstiactis in the large number of short tentacles ; from Bunodeopsis in the disposal of the phlyctenia over the whole of the column ; from Thaumactis in the lenticular form, and absence of a pedal-disc in the latter genus. For these reasons I propose for these two species a new genus, Phlyctenactis. The differences between this genus and the other four are shown by the following table : — Table of the Gknera of the Family Aliciid^. Genus. Tentacles. 1 Mesent. ^^^^^^^ Column. Pedal- disc. Alicia Cystiactis . . . . '' Few ; long Bunodeovsis . . Thaumactis . . . . \ Phlyctenactis (gen. nov.) Many ; short 6 pairs On pioximal part . . 12 pairs All ovtr i column Lenticular Cylindical Absent Present 396 Transactions. Genus Phlyctenactis (gen. nov.). AliciidcB of large size, with numerous short tentacles arranged in several cycles. Column entirely covered with simple vesicles, sessile or on short pedicles, arranged more or less in vertical rows, and communicating with the intermesenterial spaces. More than six pairs of perfect mesenteries. 21. Phlyctenactis retifera (sp. nov.). Pedal-disc. — Lobed, wider than the column. Only slightly adherent, the animal being able to " crawl " about on it, and to become free and float away at will. The colour of the pedal-disc is yellowish-orange. Column. — Cylindrical in form, and covered with large blisterlike vesicles, which in the contracted state of the animal lie in contact, but in expansion are separate. Their longitudinal arrangement is not evident, except when the animal is expanded. They open by small openings into the coelenteron. They appear to assist in the flotation of the animal. The colour of the column is dark velvety brown. The mesogloea of the wall is very thick, appearing as a homogeneous mass, bordered on each side by parallel fibres, and crossed by oblique transverse fibres. I have seen no definite sphincter, but the circular endodermal muscle of the wall is developed through its whole length. The ectoderm and endoderm of the wall are not so well developed as the mesogloea. The vesicles contain all the elements of the wall. Tentacles. — Very numerous and crowded, in about six cycles. They are simple, and conical in shape. Their colour is pale yellow. Their histology is interesting. Next to the ectoderm comes a thin layer of homogeneous mesogloea, followed by a thick layer of highly reticular mesogloea, then a thin homogeneous layer, under which is the endoderm. (Plate XXVI, figs. 1,2.) Oral Disc. — The disc is flat, with the mouth on a large mound-shaped peristome. The colour of the disc is light yellow, that of the peristome very dark brown or black. The mouth bears two bright-yellow tubercles. Stomodceum. — This is white in colour, and has a very thick layer of ectoderm. There are 2 siphonoglyphs. Mesenteries. — There are 12 pairs of complete mesenteries, which are all sterile, and 36 pairs of incomplete ones, which bear gonads. Two pairs of mesenteries are directives. The muscixlature is very weak on the complete mesenteries, stronger on the incomplete. Gonads. — Only ova were seen. These are borne in the usual way, on the imperfect mesenteries. Habits. — This anemone frequents quiet pools among the rocks, but is sometimes seen floating at the surface, oral disc downwards. Rather un- common. Dimensions. — Fully expanded the animal is 18 cm. in height and 10 cm. in diameter. Distribution. — Of the genus — New Zealand. Of the species — Cook Strait. 22. Phlyctenactis morrisonii (sp. nov.). This species was sent me (one specimen) from Stewart Island by Miss E. Morrison, M.A. It had been some time in spirit, and was not well preserved. It agreed in most respects with spirit specimens of the last species, and I have no doubt that the two belong to the same genus. It differs from the last in one important respect. The ova (which were very numerous in the Stuckey. — A Review of the New Zealand Actiniaria. 397 specimen) are borne on much-reduced mesenteries, and appear, indeed, to spring direct from the body-wall. They are arranged in plates or lamelk>, each plate consisting of a large number of strings of ova lying side by side (Plate XXVJI fig.l). In some of the tentacles I found small stones of the size of a pea. These probably came there by accident. On the other hand, they may serve a hydrostatic purpose. The colour of the specimen was purplish- blue. Distribution. — Of the genus — As above. Of the species — Stewart Island. Genus (?). 23. (?) species. This anemone, which I have been unable to classify, was found alive in the radial canal of a large acraspedote medusa at Plimmerton. It was very badly preserved when handed to me, having lain for some days in sea- water before being placed in spirit. It was good for neither dissection nor histology. The length is about 25 mm., shape cylindrical, colour white. It is not quite as thick as a lead-pencil. It was impossible to ascertain anything about the tentacles or disc. There is no indication of division into capitulum, scapus, and physa. The aboral end, however, was rounded. The column is divided by 12 longitudinal furrows. Species not seen by me. 24. Edwardsia neozealanica (Farquhar). 25. Halcampactis mirabilis (Farquhar). These species are known to exist in the neighbourhood of Wellington, but I was unable to find them, though both Mr. Farquhar and Professor Kirk (their original discoverers) accompanied me in my searches. 26. Paractis monilifera (Drayton, Milne-Edwards, Hutton), Andres regards this species as not belonging to Paractis, but to some other (unnamed) genus. 27. Actinia striata (Quoy and Gaimard, Hutton). The description of this species as given by Andres does not mention the presence of acrorhagi. He says, " II Milne-Edwards la menziona con dubbio." It probably belongs to some genus other than Actinia. 28. Phymactis polydactyla (Hutton). The disposal of the verrucse, as given by Hutton, is different from that generally given in the diagnosis of Phymactis. 29. Minyas viridula (Quoy and Gaimard, Milne-Edwards, Hutton). Andres places this species in the genus Acerominyas, which he describes as an uncertain genus. The absence of tentacles is curious, and he suggests that they may have been torn off. Apparently only one specimen has been found. 30. Sagartia crocata (Hutton). 31. Peachia carnea (Hutton). These are given in the " Index Fauna)," but the references are incorrect, and so far I have been unable to find Hutton's descriptions. Fig. 1. Edwardsia tricolor. Fig- 2. 91 Fig. 3. )J Fig. 4. »9 398 Trajisactions. EXPLANATION OF TEXT-BLOCKS. One segment of the capitulura. Musculature of a mesentery. Diagrammatic representation of portion of cross-section of a tentacle. Fig. 5. Actinia tenebrosa. Diagram showing manner of division of mesenteric filament into three branches. Fig. 6. Sagartia nutrix. Young attached to body-wall. Animal expanded. Fig. 7. Thoe albida. Diagram to show manner of deposit of pigment round bases of tentacles. Fig. 8. Thoe albida. Portion of an acontium. (From a rough slide — diagrammatic.) Tlie nerve-cells appear to be on one side, the nematocysts on the other. Fig. 9. Paractis ferax. Part of a cross-section of body-wall to show the characteristic thinning of the mesogloea at intervals. Fig. LO. Paractis ferax. Showing forking of the mesogloea in the body-wall. Fig. 11. ,, A mesentery in cross-section, sliowing parietal muscle, retrac- tor muscle, ova, and mesenterial filament. Fig. 12. Corynactis haddoni. Diagrams to illustrate the steps in lateral fission. EXPLANATION OF PLATES XXI-XXVIII. Plate XXI. Fig. 1. Sagartia nutrix photograph on a piece of seaweed. Animal partly contracted. Fig. 2. ,, Cross-section of sphincter. Plate XXII. Fig. 1. Edwardsia tricolor. Part of a cross-section, showing some of the mesenteries and ova in the body-cavity ; x 50. Fig. 2. Edwardsia tricolor. Longitudinal section of capitulum, showing ova in stomo- dseum. Plate XXIII. Fig. 1. Actinia tenebrosa. Part of a cross-section, showing one pair of directives and one siphonoglyph ; also, unequal development of mesenteries. On the right— Dirs. III. II, III, I ; on the left— Dirs. Ill, II, III, II, III, I. Note. — The junctions of the two ])airs of ]irimaries with the stomo- dseura do not show clearly in the micrograpli. though tliey were clear enough in the preparation. Fig. 2. Actinia tenebrosa. " Trefoil " of mesenteric filament. Plate XXIV. Fie. 1. Paractis ferax. Part of a cross - section, showing a mesentery with ova in an advanced stage. F'g. 2. Tealidium cinctum. Part of a cross-section, showing directives and other mesen- teries, and part of siphonoglyph. Plate XXV. Fig. 1. Cradactis plicatus. Cross-section of spliincter. Fig. 2. ,, Part of a cross-section, showing directives and other mesen- teries, and one siphonoglyph. Plate XXVI. Fig. 1. Phhjctenactis retifera. Cross-section of tentacle, showing reticular structure of the mesogloea. CJreatly magnified. Fig. 2. Portion of the same, more highly magnified. Plate XXVII. Fig. 1. Phlyctenactis morrisovii. Portion of a longitudinal section, showing body- wall, ova, and one vesicle. Fig. 2. Sagartia vagrans. Part of a cross-section, showing directives and other mesen- teries, and part of stomodanim. Plate XXVIII. Paractis ferax. Section below the stomodaeum, showing mesenteries, witli ova and mesenterial filaments ; also masses of ova between the mesenteries. Cockayne. — Some IHtherto-unrecorded Plant-hahitats. 399 Art. XXXVII. — Some Hitherto-unrecorded Plant-hahitats (IV). By L. Cockayne, Ph.D. {Read before the Philosophical Institute of Canterbury, \th November, 1908.] FiLICES. Trichomanes reniforme, Forst. f. This is an extremely rare fern in Stewart Island. Kirk (Trans. N.Z. Inst., vol. xvii, p. 230) gives Paterson Inlet and Half-moon Bay as its habitats, writing, " Restricted to a few square yards above high-water mark in each locality." Mr. J. W. Murdoch informs me it occurs at Kai- pipi Bay, Paterson Inlet. Trichomanes strictum, Menzies. Recorded by Kirk for Stewart Island only on Ulva. I have also noted it in a moist gully in the forest west of Half-moon Bay. Dryopteris Thelypteris (L.), A. Gray, var, squamulosum (Hook, f.), Schlecht. In swamp of dunes near Waikanae, Wellington. L. C. ! Blechnum Patersoni (R. Br.), Mett., var. elongatum (Mett). Forest, Kaituna Valley, Banks Peninsula. L. C. ! POTAMOGETONACE^. Potamogeton ochreatus, Raoul. Natural pond near the River Turakina, not far from its mouth. L. C. ! Potamogeton pectinatus, L. Sluggish stream near mouth of River Raugitikei, L. C. ! Cyperace^. Eleocharis neo-zelandica, C. B. Clarke. In hollows of dunes between Manawatu and Rangitikei Rivers. L. C. ! Carex dissita, Sol., var. monticola, Kuk. Subalpine meadow, Mount Anglem, Stewart Island. L. C. ! Liliace^. Phormium Cookianum, Le Jolis. (1.) Hollow in dune near mouth of River Turakina, Wellington, in company with P. tenax ; L. C. ! (2.) On cliff-faces. River Waitotara ; L. C. ! Iridace^. Libertia ixioides, Spreng. Very common in all the swampy ground amongst the dunes of the west coast of Wellington. L. C. ! 400 Transactions. Orchidace.^. Thelymitra uniflora, Hook. f. Mount Grey, Canterbury. T. Keir ! Urticace^. Urtica ferox, Forst. f. Outskirts of forest, Taumarunui. L. C. ! Elatostemma rugosum, A. Cunn. (1.) Waipoua Forest (accidentally omitted from list of species in " Eeport of Botanical Survey of Waipoua Kauri Forest "). (2.) Gullies in forest near Waitotara ; L. C. ! (3.) Eeserve on bank of River Manawatu, Palmerston Nortb ; L. C. ! LORANTHACE^. korthalsella salicornioides (A. Cunn.), Van Tiegh. Parasitic on Leptospermum scoparium, old dunes, Waikanae. L. C. ! POLYGONACE.^. Rumex neglectus, T. Kirk. Gravelly shore, Ruapuke Island. L. C. ! Caryophyllace^. Stellaria Roughii, Hook. f. Takitimu Mountains, Southland. J. Crosby-Smith ! Mount Torlesse is the southern limit in Cheeseman's Manual; Colobanthus Muelleri, T. Kirk. Centre Island and Dog Island, Foveaux Strait. L. C. ! Scleranthus biflorus (Forst.), Hook. f. Dog Island. L. C. ! Ranunculace^. Ranunculus Monroi, Hook, f., var. dentatus, T. Kirk. (1.) Mount Somers ; R. M. Laing ! (2.) Puketeraki Mountains, Can- terbury ; L. C. ! Ranunculus aquatilis, L. (Introduced.) Very plentiful in lake near mouth of River Rangitikei. L. C. ! Crucifer^. Cakile maritima, Scop. (Introduced.) Dunes, New Brighton, Canterbury. L. C. ! Not previously recorded for New Zealand. Cunoniace^. Weinmannia racemosa, L. f. Forest, Mount Grey, Canterbury. T. Keir ! RoSACEiE. Geum parviflorum, Sm. Takitimu Mountains, Otago. J. Crosby-Smith ! Cockayne. — Some Hitherto-unrecorded Flant- habitats. 401 Geum uniflorum, Buch. Takitimu Mountaiiis, Otago. J. Crosby-Smith! OXALIDACE^. Oxalis magellanica, Forst. Mount Matthews, Rirautaka Range. H. H. Travers ! Rhamnace^. Discaria toumatou, Raouh Dunes, west coast of Wellington. L. C. ! Malvace^. Hoheria sexstylosa, Col. Forest near Greymouth. H. H. Travers ! Violace^. Viola Cunninghamii, Hook. f. Swampy ground of dunes near mouth of River Turakina. L. C. ! Hymenanthera dentata, R. Br., var. angustifolia, Benth. Bank of river, Otautau, Southland. L. C. ! Hymenanthera dentata, R. Br., var. alpina, T. Kirk. Through an oversight, I stated (Trans. N.Z. Inst., vol. xl, p. 310) that Hymenanthera was not recorded for Stewart Island in Cheeseman's Manual. This is incorrect ; but the Stewart Island plant is there referred, on the authority of Kirk, to H. crassifolia, Hook. f. The plant under consider- ation occurs on Mount Anglem, but is much more abundant on the flattish ground near the stream flowing into Crooked Reach, Port Pegasus. Myrtace^. Metrosideros Colensoi, Hook. f. Forest near Waitotara. L. C. ! ONAGRACEiE. Fuchsia excorticata, L. f. Accidentally omitted from " List of Species of Waipoua Kauri Forest." HALORRHAGIDACEiE. Halorrhagis uniflora, T. Kirk. Dog Island, Foveaux Strait. L. C. ! Gunnera arenaria, Cheesem. Very plentiful in sandy hollows of dunes from Waikanae to Patea. L. C. ! Araliace^. Nothopanax simplex (Forst. f.). Seem., var. parvum, T. Kirk. Waimarino Forest, near Ohakune. E. Philipps Turner I 402 Transactions. CORNACE^. Corokia Cotoneaster, Raoul. (1.) Forest, Taihape ; E. Philipps Turner ! (2.) On old weathered rock amongst dunes near shore, a few miles south of Wanganui ; L. C. ! Myrsinace^. Suttonia nummularia, Hook. f. Almost at sea-level, near Port Pegasus, Stewart Island. L. C. ! CONVOLVULACE^. Calystegia Soldanella, R. Br. Ruapuke Island. L. C. ! BORAGINACE^. Myosotis Goyeni, Petrie. By a slip of the pen I wTote Myosotis Cheesemannii for the above \n Trans. N.Z. Inst., vol. xl, p. 313. The habitat is cliffs, Broken River, Can terbury. SCROPHULARINACE^. Mazus pumilio, R. Br. Abundant in damp ground near the coast from Waikanae to the Wai totara River. L. C. ! Veronica Petriei (Buch.), T. Kirk. Takitimu Mountains, Southland. J. Crosby-Smith ! CampanulacejE. Pratia perpusilla, Hook. f. On damp sandy ground amongst old dunes between Rangitikei and; Turakina Rivers ; not common. L. C. ! Isotoma fluviatilis (R. Br.), F. von Muell. Margin of Lake Letitia, and other places on wet ground in neighbourhood of Mount White, Waimakariri district, Canterbury. L. C. ! COMPOSITiE. Lagenophora pinnatifida, Hook. f. (1.) Beech forest, Paradise, Otago Lake district ; L. C. ! (2.) Beech forest {Nothofagus cliff ortioides), Kowai Bush, Canterbury ; L. C. ! Olearia Colensoi, Hook. f. Near summit of Mount Matthews, Rimutaka Range. H. H. Travel's '. Olearia nitida, Hook, f., var. capillaris (Buch.), T. Kirk. Waimarino Forest, near Ohakune. E. Philipps Turner ! Olearia fragrantissima, Petrie. (1.) Port Hills, Canterbury ; L. C. ! (2.) Bank of creek, Otautau, Southland ; L. C. ! Cockayne. — Some Hitherto-nnrecorded Plant-hahitats. 403 Olearia Hectori, Hook. f. Bank of creek, Otaytau, Southland. L. C. ! Olearia virgata, Hook. f. Common in many swamps amongst dunes between the Manawatu and Turakina Eivers. L. C. ! Celmisia Lindsayi, Hook. f. (?) \i I am mistaken in my identification, the plant is very close to the above. Mount Franklin, Southland. J.Crosby-Smith! Celmisia Lyalli, Hook. f. Takitimu Mountains, Southland. J. Crosby-Smith ! Celmisia viscosa, Hook. f. Takitimu Mountains, Southland. J. Crosby-Smith ! Gnaphalium trinerve, Forst. f. (?) (This mav be a form of G. leriense, A. Cunn., but it seems to me best placed as above.) On low cliff, mouth of Ototoka Stream, Oheku, near Wanganui. L. C. ! Gnaphalium Lyallii, Hook. f. Abundant in large sheets on face of cliffs near mouth of Waiongoro River, Taranaki. L. C. ! Raoulia australis, Hook. f. On rock, and also on sandy ground covered with stones near shore, south of mouth of River Waitotara. L. C. ! Senecio bellidioides, Hook. f. Canterburv Plain, at from 70 m. above sea-level, near Waimakariri River. L. C.'l Senecio latifolius, Banks and Sol. Margin of Waimarino Forest, Waimarino Plain. L. C. ! Senecio elseagnifolius, Hook. f. Mount Matthews, near summit. H. H. Travers ! Senecio cassinioides, Hook. f. Mount Franklin, Southland. J. Crosbv-Smith ! . '' 4U-i Transactions. Ar'J'. XXXVIII. — On a Collection of Plants from the Solanders. By L. Cockayne, Ph.D. [Read before the Philosophical Institute of Ganlerbury, -ith November, 1908.] The Solanders are two small islands lying in the Tasman Sea, twenty-two miles south of the southward coast of the South Island, and W. ^ 8. thirty-five miles from the north-west end of Stewart Island. The largest island, . Solander Island, is nearly a mile in length, and rises abruptly from the sea to a height of 1,100 ft. The other island, much smaller, lies a mile to the westward. On the 22nd October, Captain J. BoUons, of the Gr.s.s. " Hinemoa," while searching for a missing vessel, landed on the main island, and, eager as he always is to advance our knowledge of New Zealand natural history, made, together with Mrs. Bollons, a collection of the plants. This he was so kind as to hand over to me, and I hasten to bring before your notice this first collection of plants made on this isolated island. As seen from the appended hst, nineteen species were collected, of which four are ferns. The vegetation is evidently closely allied to that of the outlying islands of the Stewart Island group, on the one hand, and, more distantly, to the coastal scrub of the West Coast Sounds, on the other. Poa foliosa and Senecio Stewartiw also connect it with the Snares. Neither of these two plants has been found on the South Island, nor has the Senecio been recorded from Stewart Island itself, though it is fairly common, I under- stand, on the small outlying islands. The Stilbocarpa differs from that of Stewart Island, being much more hairy, of a rather dull green, and the small veins on the back of the leaf are much raised, making it almost lacu- nose. It increases by means of runners, as does the Stewart Island plant, and consequently differs altogether from the Snares plant, with its massive rhizome and no runners. A more searching examination than Captain Bollons was able to give will probably show that other plants are present. One would certainly expect Olearia angustifolia, Scivpus aucMandicus, S. cernuus, Gentian a saxosa, one or two species of Hydrocotyle, and probably certain common coastal plants ; also, the higher parts of the island not visited should have species not found at a low level. LIST OF PLANTS, Pteridophyta. Asplenium obtusatum, Forst. f. ,, lucidum, Forst. f. Blechnum durum {Moore), C. Ckr. Histiopteris incisa (Thhg.), J. Sm. Poa foliosa, Hook. f. ,, Astoni, Petrie. Carex trifida, Cav. Speraiophyta. GraminecB. Cyperacere. Cockayne. — On Aerial Rhizomes. , 405 JuncacecB. Luzula campestris, D. C, var. australasica, Buchen. (?) Orchidacece. Thelyniitra uniflora, Hook. f. * Aizoacece. Mesembrianthemum australe, Sol. Crcissulacece. Crassula moscliata, Forst. f. Araliacece. Stilbocarpa Lyallii, J. B. Armstg. Umhelliferce. Apium prostratum, Lab. Aciphylla intermedia {Hook. /.). Boraginncece. Myosotis capitata, Hook. /., var. albiflora, J. B. Armstg. ScwphularinacecB. Veronica elliptica, Forst. f. Compositce. Olearia Colensoi, Hook. f. Senecio Stewartife, J. B. Armstg. „ rotundifolius {Forst. /.), Hook. f. Art, XXXIX. — Note, on Aerial Rhizomes in Cordyline australis. By L. Cockayne, Ph.D. \Read before the Philosophical Institute of Canterhury, ith November, 1908.] As is well known, the common New Zealand cabbage-tree {Cordyline aus- tralis) sends deep down into the ground a continuation of its ordinary up- right-growing trunk, from which it differs in its positive geotropism, pos- session of roots, and rudimentary scale-like leaves. This rhizome functions not merely as an anchor for the plant, which is kept in place by the spread- ing horizontal or semi-horizontal roots ; but it serves as a storage-organ for food, on the relative amount of which depends, doubtless, the blooming of the tree. If the trunk be cut oft' below the level of the ground, new aerial negatively geotropic shoots will be produced, and, vice versa, if the cut-oft" aerial portion can be induced to grow, a new positively geotropic shoot (rhizome) will be produced at its base. Frequently the trunk will put forth from any part ordinary leafy shoots, and occasionally near its base small positively geotropic rhizomes will be developed. Some years ago the Hon. E. C. J. Stevens, M.L.C., called my attention to a fine specimen of Cordyline australis growing in the grounds of the Christ- church Club, which had a profusion of aerial rhizomes issuing from its trunk, not from near the base, but at a considerable distance from the ground. 406 Transactions. The trunk of this tree is at the present time about 34 cm. in diameter, the actual base being swollen and wider. At 1-8 m. from the ground it oives off four erect branches, and it is at this point that the bunches of rhizomes are situated, though not merely at the forking, but to within 1-25 m. from the base of the tree. Plate XXIX gives a far better idea of the appearance, &c., than any detailed description. The largest bunch of rhizorrrt's is 38 cm. long and 18 cm. deep. These bunches arise from lateral branches being freely produced, and which, through their positive geotropism, are brought close together. A rather large branch measures 18 cm. in length and 17 mm. in diameter. Short rudimentary lateral roots pass off horizontally from their sides. Eegarding the cause of this abundant growth of aerial rhizomes I can say nothing. The tree is at present rapidly dying, and the growth may be in the first instance pathological. It is not altogether dependent on the branching of the tree, since some of the rhizomes are given off far below the forking ; others, again, where there is no branching, on one of the primary branches. It is evident, however, that under certain conditions — at present unknown — Cordyline austraUs can put forth from presumably the same tissue either an ordinary leafy ascending shoot or a rhizomatous descending one. EXPLANATION OF PLATE XXIX Aerial rhizomes growing high up on trunk of Cordyline australis. Art. XL. — The Wellington Tide-gauge. By C. E. Adams, M.Sc, A.I.A. (Loud.), F.R.A.S. [Read before the Wellington Philosophical Society. 1st July. 1908.] The Wellington tide-gauge differs materially from all other tide-gauges, and, as its design avoids most of the sources of error in the usual patterns, an account of its great advantages is now submitted ; but in order to appre- ciate these advantages it will be necessary to refer briefly to the essential features of the usual forms. In vol. xvi* of the G.T. Survey of India it is stated that " the object aimed at in any complete system of tidal observations is to obtain the height of the tide above some fixed m.ark or datum for every instant of time during a more or less extended period. . . . This object is attained graphic- ally by causing the rise and fall of the water to communicate its motion, by mechanical means, to a pencil which traces a line on paper wound round a drum turned by clockwork once in twenty-four hours. . . . An instrument such as above briefly described is called a self-registering tide- gauge, and of these various forms have from time to time been constructed. The best form is, according to the opinion of Sir William Thomson, one in which the drum is inclined to the vertical, as this enables the friction between the pencil and the paper to be nicely regulated. The pattern almost ex- * " Details of Tidal Observations," p. 9. y, o > 'f. z < -rJSfc^^-V^.JSlR^^ c o in < m D < 2 Q o u 2 O m W o N ft; < < Face p. 406. Adams, — The Wellington Tide-gauge. 407 clusively used in India is that known as Newman's pattern, in which the drum is horizontal, the only exception being a small gauge at Prince's Dock, Bombay, where the drum is vertical." Full details of the Indian gauges are given in vol. xvi, while a description of the Newman gauge is also given in Baird's Manual.* The horizontal drum of the Newman gauge is 5 ft. 3 in. long, and exactly 21 in. in circum- ference. The drum revolves by clockwork once a day, and has attached to it the record-paper. A pencil moves in a slide along the top of the drum, and to the pencil-carriage a wire is attached which is actuated by the float through cog-wheels. In this arrangement there are many defects : " First, the drum for the diagrams was not quite circular in section, the ellipticity in some cases being very marked. Secondly, the drum was not stable in every position of its revolution — i.e., when disconnected from the clock and turned by hand it assumed a certain position of its own accord." To overcome the first defect it was necessary to make the clerk in charge mark the exact position of the pencil on the diagram at four different times of the day, then to redivide the diagram from these marks. Thus the whole advantage of a ruled diagram was lost, as also many of the advantages of a self-registering gauge, as constant attention of the clerk in charge is required. The second defect was ingeniously overcome by a special back- lash w^eight. There were many other defects, particularly in the adjust- ment of the drum in relation to the clock, and to overcome all these defects so many additions were necessary as to render the gauge a complicated piece of mechanism requiring skilled attention. In the Indian gauges constant attention is required to prevent the error of the clock becoming serious. The duties of the clerk in charge of an Indian tidal observatory involve constant attendance at 7 and 10 a.m. and 4 and 6 p.m. daily, and where labour is cheap (£2 to £2 10s. per mensem) this attention can be easily arranged for ; but in other parts of the w^orld gauges requiring less attention are necessary. Fig. 1. (Scale, l,OOO.ft. to an inch.) The Wellington tide-gauge was designed by Mr. William Ferguson, M.A., M.Inst. C.E., formerly Engineer and Secretary to the Wellington Harbour *"A Mamial for Tidal Observations," by Major A. W. Baird. London: Taylor and Francis, 1886. 408 Tratisactioiis. Board. It was erected in 1887, and is at present situated in N shed, on Jervois Quay, Wellington, as shown in fig. 1. The general design of the gauge is shown in fig. 2. The cylinder or drum is 4 ft. long and 0-4 ft. in diameter.* It is horizontal, and carries a wheel 2-4 ft. in diameter on the end of its axle. The float is attached by a band to the circumference of the wheel. A smaller wheel carries a counterweight to keep the float-band always taut. The pencil-carriage moves horizontally at a uniform rate, and is in train with the driving-chain of the eight-day lever clock. Its motion is approximately 6 in. a day, so that one week's record is obtained on the drum. It will be seen that the design of this gauge avoids all the defects of the Newman and other forms of gauge. Thus, owing to the smaller diameter of the drum, it can be readily turned truly circular, and, as it is the amount of motion under the pencil that has to be measured, small ellipticity of 3f< Floit ScsU of Feel Fig. 2. — The Wellington Self-eegistering Tide-gauge. section does not vitiate the record, and, althovigh the drum is naturally turned as evenly as possible, any defect in balancing is immaterial, as the counterweight can be adjusted to overcome it. It is, however, in the ad- justment of the time that the greatest improvement becomes apparent. The clock is wound up once a week, and when wound up the pencil-carriage is drawn to the left end of the drum. A new record-paper is attached to the drum, which is then revolved underneath the pencil, and on the line so drawn the correct local mean time is written, independent of what time is shown on the clock. At the end of the week the drum is again turned round, * Tiie range in Wellington is about 4 ft. or 5 ft., so that wlien used elsewhere the ratio of the diameters of the drum and wheel must be altei-ed to keep the record within practical limits. Adams. — Tit" Wellington Tide-gaiiye. 409 so that the pencil draws a second line : the correct local mean time is written on this line, and again no record is made of the time shown on the clock. In fact, the sole purpose of the clock is to give uniform motion to the pencil, and so long as the clock's rate does not materially vary the record will be correct. And at any time during the week a check line can be similarly drawn, and the correct local mean time noted on it. A check on the rate of the clock is obtained by measuring the distance between the end lines on the record. Fig. 3 shows a portion of the record of this gauge, beginning 1908, July 11. The first line was drawn at 9.55 a.m., and a check line is shown at 11.45 a.m. The last line (not shown) was drawn on July 18 at 9.20 a.m., while other check lines (not shown) were drawn on July 14 at 12.40 and 13.00. The lines showing midnight are drawn in by scale from the first and last lines on the diagram. ^Feet Vertical Scale Fig. 3. Particulars of the Wellington gauge were recently sent to Sir G. H. Darwin, who replied, " I never heard of a tide-gauge such as that you describe, but there seems no reason why it should not work very well." Harmonic Tidal Constants. Through the courtesy of Mr. Thomas Wright, of " Lyndhurst," Victoria Drive, Eastbourne, Sussex, the harmonic tidal constants for Wellington and Auckland are here recorded. Mr. Wright states, " They have been obtained by the aid of Grovernment grants from the Royal Society, and were deduced by methods devised by Sir G. H. Darwin, and will be presented for publication in the Proceedings of that Society. The constants for Wel- lington were obtained from twelve months' observations, the epoch to which 410 T rcnisactions . the figures refer being 1901, January, 1 d. 0 h. The constants for Auckland were obtained from observations covering a period of the same length, the epoch being 1900, May 1." New Zealand Ports. — Harmonic Tidal Constants for Auckland and Welling- ton (deduced from High- and Low-water Observations). Auckland. WelUnetou. Epoch 1900, May 1. Epoch 1901, January 1. H. K. H. K. Tide. Feet. Degrees. Feet. Degrees. Tide. S2 . 0-6.33 266 0-11 308 . Sa Ma . . 3-826 205 1-70 123 . M., 0 Neglect. 0-13 194 . 0 Ki • . 0-265 169 0-18 275 . Ki K2 . . 0-172 266 0-03 308 . K2 P . 0088 169 0-06 275 . P L . 0-164 196 Neglfct. L N . 0-778 175 0-45 S3 . N Sa . . 0-354 139 007 295 . Pa Ssa ■ . 0-224 242 0-20 212 . Ssa Ao = 5-871 ft. Ao = 37-74 ft. Art. XLI. — A Natural Classification of English Poetry. By Johannes C. Andersen. [Read before the Philoso'phical Institule of Canterbury, 5th August, 1908.] The discovery of the law guiding the formation of verse-lengths suggested in the paper on " Origins of English Metre," read last session, has made it possible to scheme out a natural classification of the whole of Englisli poetry. For purposes of classification it is necessary to fix on some characteristic common to all species — a characteristic which, whilst it varies, does so in a regular manner, so that, whilst the characteristic itself is not perfectly constant, each variation is constant in itself. In poetry the problem has been to detect such a characteristic in the midst of an apparent maze of variations. One classification attempted has been according to quality — that is, all lyrics, including songs, odes, sonnets, have been grouped together ; didactic poems, narrative, epic, dramatic, and so on : but this is similar to classifying flowers by their hues and scents. Again, another classification has been according to the number of stresses in a line as printed ; so that one class included one-stressed or two-syllabled lines, another three-stressed, another four-stressed, and so on : this, too, is artificial, though it is nearer Andkesen. — Natural Classification of English Poetry. 411 the true classification : as in the system of Linnaeus, the true organs have been taken, but classification has been by their number instead of by their development. • Under the breath-law, the various poetic forms in use aroup themselves into certain evident classes. This law indicated the first great characteristic — the length of line ; and this gives two distinct classes — lines of five stresses and lines of eight stresses, each of which two classes I have named after their predominant types, Heroic and Ballad respectively. Setting aside the internal syllabic variation of verse, the places of greatest variation are at the beginning and end of lines. Variation at the end being the more pronounced, this has been taken as the distinguishing feature of the various ballad forms into which the Ballad class has been divided, and the varia- tion at the beginning as the feature of the subvariations of the different forms. Thus in Romance Metre, or Parent Ballad, the line-end may lose a stress-unit, or foot, and become Popular Ballad, of seven instead of eight stresses. In the Popular Ballad, again, there are two variations — in one the stressed syllable at the end of every half-line is dropped, in the other the whole unit at the end of every half-line. These two forms would have been kept as subvariations of the Popular Ballad were it not for the fact that the former constitutes the normal ballad-metre of Denmark and Ger- many— and from the epic of the Nibelungen Noth being written in it I have called it the Nibelungen Metre — and the latter constitutes the ballad- metre of France, and has already been called the Alexandrine, from its forming the metre of a French epic on the deeds of Alexander. The stress-unit at the beginning of the line can be varied only in two ways. In its normal form it consists of two syllables, the first unstressed, the second stressed. The unstressed syllable may be dropped, or it may be preceded by an extra unstressed syllable : from these variations are produced the subvariations in each of the Ballad forms. Minor variations are formed by adding or dropping syllables at the line-ends. Thus, in Romance Metre an unstressed syllable may be added, when what is called a feminine or weak ending is produced. If it drop a syllable, it produces feminine Popular Ballad ; if it drop two syllables, it produces ordinary Popular Ballad. If Populai' Ballad drop a syllable at the half-line end. it produces Nibelungen. If Nibelungen drop a syllable at the half -line end, it produces Alexandrine ; if it add a syllable at the line - end, it produces either feminine Nibelungen or feminine Alex- andrine. Though these comprise the whole of the variations, except the internal syllabic variations which are rather to be considered as scent and colour, it will be seen that they include all regular formations outside lines of five stresses. These latter form the second great class, the Heroic. This does not show nearly the amount of variation of line-end shown by the former ; its lines contain within themselves other and more subtle means of variation, such as pause, overflow, &c. — features practically denied to Ballad. Its subdivisions will be more readily seen. Firstly, the Common Heroic includes all poems in riming couplets, with a sub variation including riming stanzas, such as Spenserian, Sonnet, Rime Royal, &c. Secondly, Blank Verse in- cludes two divisions — Epic, Narrative, and Didactic poems ; and the Drama, rimed or unrimed. A third class, which I have called Irregular, includes the Ode, poems in which the length of line follows no one of the preceding classes exclusively, Metrical Tales, and Songs ; a subdivision I have called Prose Lyrics, to include much of Walt Whitman's poetry ; another division 412 Transactions. will contain those eccentricities, once popular, where poems are \vritten in the shape of diamonds, crosses, pyramids, and so on. A subclass will contain Exotics, such^ as the Rondeau, Rondel, Ballade, Villanelle, &c. The following table shows the classification in a concise manner, the name of a specimen poem being quoted with each by way of illustration : — Class I. — Ballad. A. Native. 1. Eight-stressed lines (16-syllabled) = Romance Metre (Parent Ballad) — (a.) Continuous. (Gower's " Confessio Amantis.") (6.) Stanzaic. (Burns's " Ye Banks and Braes.") 2. Seven-stressed lines (14-sylIabled) = Popular English Ballad — (a.) Continuous. (All old ballads before printing.) {h.) Stanzaic. (Coleridge's " Ancient Mariner.") 3. Seven-stressed lines ( 1'3-syllabled) = German Ballad : Nibelungen — {a.) Continuous, (ffihlenschk'ger's " Hrolf Krake.") (&.) Stanzaic. (Macaulay's " Horatius.") 4. Six-stressed lines (12-syllabled) = French Ballad : Alexandrine — {a.) Continuous. (Drayton's " Polyolbion.") [h.) Stanzaic. (Shelley's " Indian Serenade.") B. Exotic. 1. Six-stressed lines (syllables indefinite) = Greek Ballad : Imitation of Hexameter. (Longfellow's " Evangeline.") Class II. — Heroic. (All fines of five stresses.) 1. Heroic Couplet — {a.) Continuous. (Pope's " Essay on Man.") (6.) Stanzaic. (Rime Royal, Spenserian Stanza, Sonnet, Ottava Rima, &c.) 2. Blank Verse— («.) Epic, Narrative, Didactic, Descriptive. (Milton's " Paradise Lost," Browning's " The Ring and the Book," Young's " Night Thoughts," Thomson's " Seasons.") (&.) Drama. (Shakespeare, Marlowe, &c.) Class III. — Irregular. A. Native. 1. The Ode— (a.) Ode, Song, Metrical Tale. (Dryden's " Alexander's Feast," C. Rossetti's " Echo," Southey's " Curse of Kehama.") (&.) Prose Lyrics. (Whitman's " President Lincohi's Burial Hymn.") 2. Artificials — Poems in shape of diamonds, crosses, &c. (Herrick's " Cross," Withers's " Diamonds.") B. Exotic. Rondeau, Rondel, Triolet, Ballade, Villanelle, Virelai, Pantoum, &c. Andtrsen. — Natural Classification of English Poetry. 413 Lost those subdivisions appear at first sight very limited, the further subdivisions of Division 1 of the Ballad may be shown : — Division 1 of Class I, Ballad. (a.) Continuous. (].) Long Verse. (Tennyson's " Locksley Hall") (2.) Split— " ' {a.) Ordinary (iambic). (Butler's " Hudibras.") (h.) Abrupt (trochaic). (Shelley's " Lines written Euganean Hills.") (3.) Trisyllabic. (Goldsmith's " The Retaliation.") (b.) Stanzaic. among the IT. A. 1. (a.) ■■/ (h.) ■• / {<-'■) ••/ id.) / ■ • ■ / (c-) ...■/ 2. (a.) .. / (b.) .. / (c.) .../ 3. (a.) ••/ (h.) ••/ (c.) .../ B. 1. {a.) ../ (&.) ••/ (c.) ••/ (d.) .-./ (e.) .../ 2. (fl.) ••/ (b.) ••/ ic) .../ 3. (a.) ../ (b.) ••/ (c.) / • ' • / C. 1. (a.) ••/ A. 1. (a.) •/ (h.) ■/ (c.) ./ 2. (a.) ./ (b.) •/ 3. (a.) ./ (b.) ./ B. L (a.) ./ (&.) •/ (c.) ./ 2. (a.) ./ (&.) •/ 3. {a.) ./ (b.) ./ 0. 1. (a.) ./ •/ • •/ ../ . ./ . •/ •• . . / . . •/ •• •/ • / * • / . / .. ./ ... ../••• ./... . /.. ../... . / . . . ./.... ../ .. •/ •• / ../ .. •/ •■ ./ ... . . / ... / • / • • • . / .. ../... ./... ./.... •■/ • ./ . / • / ./ ■ •/ • ./ .. ../ .. . / .. / / ./ .. ./ .. ./ ... ../ .. •/ ■• ./ ./ .. •/ •• ./ ... ../ . ./ • •/ • ../ . •/ • ./ .. ../ .. ■/ ■• ./.. .. / .. ./ .. ./ ... ../ .. ./ .. ./.. ../ .. ./ .. . / ... ../ . •/ • •/ ••/ • •/ ■ ./ .. ../ .. . / ./ • ../ .. ■/ •• ./ ... ../... ./... ./.. ../... ./... ./.... .. / .. ./ .. •/ • ../ .. ./ .. ./ ... .. /... ./... ./.. ../... . /... ./.... ../ . ./ . ./ ./ . . / . ./ .. / • • / ./ .. •/ • / • • ./ .. ./ ... ../ .. . / .. •/ ./ .. ./ .. ./ ... ../ . •/ • •/ . ../ . •/ • •/ •• ../ .. ./ .. ./.. ../ .. •/ •• ./ ... ../ .. ./ .. ./.. ../ .. ./ .. ./ ... ../ . •/ . •/ ../ . • / • ./ .. ../ . •/ • •/ .. / . •/ • ./ .. ../ .. ./ .. ■/ . ../ .. •/ •• ./ ... ../... ./... . / .. ../... ./... ./.... ../ . ./ . •/ ./ • •/ • ./ .. ../ .. ./ .. •/ ./ .. ./ .. . / ... / •/ • •/ . ../ . •/ • ./ .. ../ .. ./ .. ./.. ../ .. ./ .. ./ ... ../ . •/ . . / ../ . •/ . ./ .. ../ .. ./ .. •/ • ../ .. ./ •• ./ ... ../... ./... ./.. ../... ./... ./.... ../ . . / . ■/ ./ . •/ • ./ .. ../ .. ./ .. ■/ ./ .. •/ •• ./ ... ../ . . / . •/ • ../ . ■/ • ./ .. ../ .. ./ .. ./.. ../ .. •/ .. ./ ... ../ . •/ . . / ../ . ./ . ./ .. / (1) / (2) / (3) / (4) / (5) / (6) / (7) / (8) / (9) / / (10) / (11) / • (12) / . (13) / . (14) / / (15) / (16) / (17) / (18) / (19) / (20) / (21) / . (22) / .(23) / (24) / (25) / (26) / (27) / (28) / (29) / (30) / • (31) / (32) / (33) /■ (34) / (35) /• (36) /• (37) / .(38) 41tl: Transactio7is. In the above table the units, of which there are eight in the Romance Metre, are divided ofi by the /, the syllable preceding the bar bearing the stress in every case : each . represents a syllable. Example (1) is then ordinary duple, or iambic metre ; (2) is ordinary triple, or anapestic metre, with iambic opening ; (3) is ordinary quadruple with iambic opening ; (4) is pure triple ; (5) is quadruple with triple open- ing ; (6) is ordinary duple, the second half-line beginning abruptly, or with a stressed syllable ; (9) is ordinary duple with a feminine first half-line, producing a triple unit in the middle of the verse. Class B, (12) to (22), is exactly the same as Class A, (1) to (11), except that all the varieties in the former have feminine verse-ends. Class C (23) may be extended in a similar way of Classes A and B ; it differs from them in the verse ending with a double feminine, but this is of such rare occurrence that, unless specimens are actually found or made, it is unnecessary to cite the various varieties, all of which are, however, possible, and occur often enough in isolated couplets in eccentrics such as the " Ingoldsby Legends." Group II, again, is similar to Group I, except that throughout the former the beginning of the verse is abrupt — that is, it begins with a stressed syllable ; so that, whilst Group I contains the so-called iambic and anapestic metres, Group II contains the trochaic and dactylic. Those above tabled are the main variations. There are intermediate forms ; for example, betw^een (1) and (2) the following form often occurs : — _../ .../ .../ .../ ../ .../ ._../ .../ where both half-lines of the triple metre begin with a duple unit. The extremes of variation only are given in the table, intermediate forms readilv falling into their places. It must be noted, however^ that it is as much the exception as the rule to find verses entirely in any one of the above varieties. They may change from one to another, or hover around several of the forms in each of the Divisions A, B, and C, but they can always be readily assigned their place in the scheme. For instance, Shelley's " Sensitive Plant " is a mixture of duple and triple metre : — A Sensitive Plant in a garden grew, And the yoi ng winds fed it with silver dew, And it opened its fan-like leaves to the light. And closed them bereath the kisses of night. This, divided into units, reads, — A Sen/sitivo Plant/ in a gar/den grew/, and the young/ winds fed/ it with sil/ver dew/. And it o/pened its fan-/like leaves/ to the light/, and closed/ them beneath/ the kis/ses of night/ or ../.../.../ ../.../ ../.../ ../ .../.../ ../ .../ ../.../ ../.../ It will be seen that it hovers between (a) and {d) — (1) and (4) — of Group I,^ Class A, Division 1. The various divisions of the table have been made, as there is a vast number of poems that can be wholly placed in one or other of them. In the quotations following, the numbers correspond with the numbers of the variations in the table : — (1.) Ye banks/ and braes/ o' bon/nie Doon/, how can/ ye bloom/ sae fresh/ and fair ? Andersen. — Natural Classification of English Poetry. 415 (2 (3. (4. (5. (6. (7. (8. (9. (10. (11. (12. (13. (15. (16. ;i7. (20. (21. (22. '23. ,24. (25. (27. (28. (29. (31. Our bu/gles sang truce/ for the niglit-/C'loud had hnvei'd/. and the sen/tinel stars/ set their watch/ in the sky/. An' half/ our buUicks per/ished when the drought/ was on the land/, an' the burn/in' lieat that daz/zles as it dan/ces on the sand/. The Assy/rian came down/ like a wolf/on the fold/, and his co/- horts were gleam/ing in pur/ple and gold/. And the bush/ hath friends to meet/him and their kind/ly voices gi-eet/ him in the mur/mur of the breez/es and the riv/er on its bars/. Since when/ all songs/ for jo/ vial souls/ hav/ing no/thing, thought/divine/. As gay/ as a lark/, and as blythe/ as a bee/, hand/some, gen/erous, spright/ly, and young/. I have read/her roman/ces of dame/and knight/; she/was my prin/cess, my pride/, ray pet/, Wlien love/ly wo/ man stoops/ to fol/ly, and finds/ too late/ that men/ betray/. Then up/ with the Bau/ner, let fo/rest winds fan/ her, she has blazed/ over Et/trick eight a/ges and more/. Of the mail/ cover' d ba/rons, who proud/ly to bat/tie led their yas/sals from Eu/rope to Pal/estine's jilain/. And is/ she dead ?/ and did/ they dare/ obey/ my fren/zy's"jea/- lous ra/ving ? The pine/ boughs arc sing/ing old songs/ witli new glad/ness, the bil/lows and f oun/tains fresh mu/sic are fling/ing. At the dance/ in the vil/lage thy white/ foot was fleet/est ; thy voice/ 'mid the con/cert of maid/ens was sweet/est. And the daugh/ter3 of the Var/dens — they_ are beau/tiful as Gra/ces — b\it the bal/cony's deser/ted, and they rare/ly show their fa/ces. Awake 1/ my love/, the sun's/ bright ray/, hill/ and yal/ley's now/adorn/ing. Her voice/ did cpii/ver as/ we part/ed, yet knew/ I not/ that heart/was brok/en. _, The soul/ speaking eyes/ are the lan/guage of bliss/es, and we'll talk/ with our eyes/ amidst si/lent kiss/es. Though thy beau/ty must fade/, yet thy j'outh/ I'll remem/bcr; that thy May/ was my own/ when thou show/est Decem/ber. The coach/man then held/ the door fast/ in his hand/, to let/ me get out/ he was not/ at all wiU/ing. sirs. Oh, I'm/ call'd the Ja/nus, the pride/ of gentil/ity. as jus/tice I act/. I'm sure/, with abil/ity. As the wise/, brave, and good/, of thy frowns/ seldom shape/ any, witness brave/ Belisa/rius, wlio begged/ for a ha'-/)ienny. Aske/ me why/ I send/ you here/ this sweet/ Infan/ta of/ the yeere ?/ Bird/ of the wil/derness, blith/some and cum/berless, light/ be thy ma/tin o'er wood/land and lea !/ Must/ thou go/ my glo/rious chief/. se/ver'd from/ thy faith/- f ul few ?/ Hie/ upon Hie/ lands and low/ upon Tay/, bon/nie George Cara]3/bell rode oiit/ on a day/. God/ be with/ thee, glad/some o/cean ! how glad/ly greet/ I thee/ once more !/ .; There's/ a wo/man like/ a dew-/drop, she's/ so pur/er th.an/ the pur/est. ^ '<^/-^ -^.•-^ V ^ luIlIBRAR Y 1^ 416 Transactiom. (32.) F?ir/ stood the wind/ for Fi'poUce, when/ we our sails/ advance, nor/ now to prove/ our chance iong/er we tar/ry. (34.) My/ dear Mis/tress has/ a heart/, soft/ as tliose/ kind looks/ she gave/ me. (35.) Howl/ not, ye winds/, o'er the tomb/ of the brave/ ; roai'/ not, ye waves/, at the foot/ of the monn/tain. (3G. ) 1/ will an/swer. These/ discov/er what faint/ing hopes/ are in/ a lov/er. There are several intermediate forms, of w^hicli entire poems are composed, and it might be found advisable to make divisions for their insertion. For example, the following form the scheme of well-known poems : — Between (1) and (2), — 0, young/ Lochinvaa-/ is come out/ of the West/ : through all/ the wide Bor/dor his steed/ was the best/ ; Between (12) and (13),— Oh, say/ not, sweet Anne/, that the Fates/ have decreed/ the heart/ which adores/you should wish/ to dissev/er ; Between (24) and (25),— Bright/est and best/ of the sons/ of the morn/ing 1 dawn/ on our dark/ness and lend/ us thine aid/ ; Between (31) and (32),— Where/ shall the lov/er rest, whom/ the fates sev/er from/ his true maid/en's breast/, parted for ev/er ? There are fitrther irregular variations, as when Romance Metre mixes with Ballad or Alexandrine. Ballad with Alexandrine or Nibelungen, &c. The table shows only regular forms ; the irregular, whilst they could be classified, are hardly of sufficient importance to warrant more than one general sub- division. Poems in regular structure vastly predominate, and it is, indeed, only because this is so that it has been found possible to compile the table. Each of the other Ballad forms — Ordinary, Nibelungen, and Alexandrine — vary in the same wav, though not to the same extent, as the Romance Metre. The stanza form has not been taken as a standard of classification, as it varies in a manner altogether arbitrary : the line formations follow a definite law, and their variations from this law can readily be perceived. The stanza, on the other hand, appears to follow no fixed law, though it is a curious fact that the normal stanza of. all the Ballad metres is composed of eight half-lines, and the parent Ballad line of eight stresses. The forma- tion of the line is primarily rhythmical, then syntactical ; the formation cf the stanza appears to be primarily syntactical. A few normal stanzas are quoted, to show the variation of form that may take place within the same metrical scheme : — Variation (1). Ye banks and braes o' bonnie Doon, How can ye bloom sae fresh and fair ? How can ye chant, ye little birds. An' I sae wea,ry, fu' o' care ? Thou' It break my heart, thou warbling bird. That wantons thro' the flowering thorn : Thou minds me o' departed joys, Departed, — never to return. (Burn«, " The Banks o' Doon.") Andersen. — Natural Classification of EngJ,ish Poetry. 417 She's mounted on her milk-white steed, And she's ta'en Thomas up behind ; And aye, whene'er her bridle rang, The steed gaed swifter than the wind. 0 they rade on. and farther on. The steed gaed swifter than the wind ; I'litil they reached a desert wide. And living land was left behind. (" Thomas the Rhymer.") From Oberon, in fairj^e land, The king of ghosts and shadows there. Mad Robin I, at his command, Am sent to viewe the night-sports here. Wliat revel rout Is kept about. In every corner where I go, I will o'ersee. And merry bee. And make good sport, with ho, ho, ho I ("Robin Good-Fellow.") With deep affection. And recollection, [ often think of Those Shandon beUs, Whose sounds so wild would. In the days of childhood, Fling round my cradle Their magic spells. On this I ponder Whene'er I wander. And thus grow fonder. Sweet Cork, of thee ; With thy bells of Shandon, That sound so grand on The pleasant waters Of the river Lee. (P. Mahony, " The Shandou Bells.") Variation (2). Our bugles sang truce, for the night-cloud had lower' d. And the sentinel stars set their watch in the sky ; And thousands had sunk to the ground, overpower' d, The weary to sleep and the wounded to die. Wlien reposing that night on my pallet of straw, By the wolf -scaring fagot, that guarded the slain, In the dead of the night a sweet vision I saw. And thrice ere the morning I dreamt it again. (Campbell, "The Soldier's Dream.* ,, (Half-stanzas.) The glad birds are singing. The gay flowrets springing, , O'er meadow and mountain and down in the vale ; The gi-een leaves are bursting ; My spirit is thirsting To ba'sk ir the sunbeams, and breathe the fresh gale. (Barton, "Spring.") By love and by beauty, By law and by duty, I swear to be true to My Eppie Adair ! 14— Trans. 418 . Transactions. I A' pleasure exile me, Dishonour delile me. If e'er I beguile thee. My Eppie Adair ! (Burns, " Eppie Adair."' >^_' " Variation (4). (Half-stanzas.) The Assyrian came down like a wolf on the fold, And his cohorts were gleaming in purple and gold. And the sheen of their spears was like stars on the sea, \Vlreu the blue wave rolls nigltly on deep Galilee. (Byron, "The Destruction of Sennacherib.") 'Tis the last rose of summer Left blooming alone ; All her lovely companions Are faded and gone ; No flower of her kindred No rosebud, is nigh, ■^ To reflect back her blushes Or give sigh for sigli. (Moore, " The Last Rose of Summer.") It will be seen that the same rhythm runs through all these examples, the variations being external — as it were in the matter of scent and colour. Besides showing poets and others what forms had been much or little used, a classification of English poetry on these lines might lead to the dis- covery of yet more laws guiding its growth. Art. XLII. — Development of Four-syUabled Metrical Unit in the Australian Modification of the English Ballad. By Johannes C. Andersen, [Read before the Philosophical Institute of Canterliury, 5th August, 1908.] Between every two beats or stresses which distinguish poetry from prose there are found a comparatively regular number of syllables ; and each stress, with the syllables between it and the adjoining stress, either behind or before, constitutes the most elementary unit in verse, usually called a "foot." These feet, which will be hereafter called "stress-units," or "units," have been classified, according to the position of the stress, and according to whether they contain two or three syllables, as iamb, trochee, anapest, amphibrach, and dactyl. As pointed out in the paper of last session, these may be resolved to two fundamental units — the iamb, and its extension the anapest ; and the stress is always on the last syllable of the unit, which I have therefore called "stress-unit" in preference to "foot." For the purposes of the present paper it is necessary only to state that so greatly do two- and three-syllabled, or dissyllabic and trisyllabic, units preponderate in English poetry that they are commonly held to be the only units, though the existence of a four-syllabled unit is admitted. As, however, when such units do occur in good verse it is Andeesen. — Development of Four-syUahled Metrical Unit. 419 almost always in isolation, they have been regarded as accidental rather than intentional. They may be found in the old ballads, in Shakespeare and in Milton ; but they have such a " rapid " effect that except in very few cases they are displeasing. Whilst there is no doubt that it has never been extensively employed as a basic unit in the poetry of Britain, the case is different as regards the poetry of Australia, where it has become the basis of the most popular of the colonial metres. The poetry most in favour in Australia is that which in spirit approaches the old English ballad, though it must be confessed it is the degenerate ballad that has exerted most influence — the " Robin Hood" type rather than the " Glasgerion," "Clerk Saunders," or "Wife of Usher's Well " type ; but there is this to be said : that it is rather the form of the type than its matter that has exerted the influence. Three-syllabled units constantly occur in even the best ballads, and, where artistically used, with most pleasing effect : they impart a " rapid " movement to the metre ; and when the themes become more common- place, more humorous, treating as they do of the lighter rather than the tragic side of life, this rapid movement becomes more and more marked, until many of the ballads are entirely trisyllabic. Though the four- syllabled unit is more rapid even than the three-syllabled, it did not evolve from the three-syllabled, and is more rarely found in that metre than in the two-syllabled. The popular poetry of Australia is undoubtedly humorous, and it was to be expected that the humorous metre of England would exert its influ- ence on the Australian poet, on account of its lively movement if for no other reason ; and in Lindsay Gordon, who has been called the father of Australian poetry, out of his sixty-seven collected poems forty-five are three-syllabled, whilst only eighteen are two-syllabled. In four poems there can be traced the germ of what was to become a dominant metre : these four are '" Unshriven," " Whisperings in Wattle Boughs," " A Hunt- ing Song," and the well-known poem " The Sick Stockrider." The new metre is most likely to result from poems MTitten in what are called tro- chaics, or two-syllabled feet stressed on the first syllable : in such cases the first and every alternate stress are dropped. In the poems of Kendall, the most truly poetic of the older Australians, there are twelve in these trochaics ; but in no instance does the metre lapse into the metre under discussion, the four-syllabled. It is different when we turn to later writers, well-known favourites such as Paterson and Lawson. Paterson's first book opens with and takes its name from a piece in this very measure, "The Man from Snowy River." Here the beat is much more distinct than in Gordon : — There was movement at the station, for the word had passed around That the colt from old Regret had got away, And had joined the wild bush-horses — he was worth a thousand poimd, So all the cracks had gathered to the fray. All the tried and noted riders from the stations near and far Had mustered at the homestead overnight, For the bushmen love hard riding where the wild bush-horses are. And the stock-horse snuffs the battle with delight. The usual reading of this stanza would require a stress on the first, third, and every odd syllable ; but on an actual reading a very different result ensues. The first two Hnes are read — There was move/ment at the sta/tion, for the word/ had passed around/ That the colt/ from old Regret/ had got away/. 420 Transactions. There is a slight stress on " passed," " old " and " got," but otherwise the lines fall perfectly naturally into four-syllabled units, giving lines of alternately four and three stresses — nothing more than English ballad-metre : in fact, the whole stanza is a perfect bal'ad stanza, but with four-syllabled units. In Paterson's two volumes of poems, out of their eighty-one pieces there are twelve in the four-syllabled metre ; in Lawson's two volumes, out of ILi pieces no less than twenty-eight bear the unmistakable stamp of this metre ; Ogilvie has eleven out of a hundred ; Boake four out of thirty- two ; Brunton Stephens the high average of twelve out of fifty-seven. Two pieces may be taken as contrast. In Kendall's imaginative poem ^' Hy-Brasil " occur the lines, — There iudeed was singing Eden, where the great gold river runs Past the porch and gates of crystal, ringed by strong and shining ones ! There indeed was God's own garden, sailing down the sapphire sea — Lawny dells and slopes of summer, dazzling stream and radiant tree I Here it is impossible, except perhaps in two instances, to slur the stressed odd syllables ; but read in the same way the following stanzas from Law- son's " Australian Bards and Bush Reviewers," and instead of humorous they are ridiculous : — ■ If you sing of waving grasses where the plains are dry as bricks. And discover shining rivers where there's only mud and sticks ; If you picture " mighty forests " where the mulga spoils the view — You're superior to Kendall, and ahead of Gordon too. Two British poems containing suggestions of the metre are the Hon. Mrs. Norton's " Bingen on the Rhine," and S. Ferguson's Irish ballad " The Fairy Thorn." A stanza from each follows : — A soldier of the Legion lay dying in Algiers — There was lack of woman's nursing, there was dearth of woman's tears ; But a comrade stood beside hiiu while his life-blood ebb'd away, And bent, with pitying glances, to hear what he might say. The dying soldier falter'd, as he took that comrade's hand. And he said. " I never more shall see my own, my native land ; Take a message and a token to some distant friends of mine. For I was born at Bingen — at Bingen on the Rhine." They're glancing through the glimmer of the quiet eve. Away in milky wavings of neck and ankle bare ; The heavy-sliding stream in its sleepy song they leave. And the crags in the ghostly air. Scott has a rare example of the metre appearing in three-syllabled sur- roundings : — He is gone on the mbnntdin, He is Uist to the ibyefit. Like a .sTonmer-dried fbautnin. When our need was the sorest. The fount reappear/n.*/ Fr(wi the ?v(U)-drops shall hbrrow, But to lis comes no cheermg. To Duncan no morrow ! When found in three-syllabled metres its existence can be shown to be accidental rather than intentional. The poet has made feminine or weak rimes at the half-line or line-endings, as in the example given, and, an ana- pest following, a four-syllabled unit results. A line from the Irish ballad " Mary le More " shows this :— As I stray'd o'er the common on Cork's rugged hbrder, IJ hile the rfejc-drops of morn the sweet primrose array'd. Andersen. — Developvient of Four-syllabled Metrical Unit. 421 It is usually avoided by making the first unit of the line an iamb instead of an anapest, as in the last line in the example from Scott, and in most lines of the ballad " Mary le More." Longfellow's " Belfry of Bruges " would receive strange handling from a four-syllabled Australian. Instead of — ■ In the market place of Bruges stands the belfry old and brown ; Thrice consumed and ihrice rebuilded. still it watches o'er the town. As the summer morn was breaking, on tl:at lofty tower I stood, And the world threw off the darkness, like the weeds of widowhood. it would be read — In the nn\r/ket place of Bru/ges stands the bel/fry old and brown ;/ Thrice consumed/ and thrice rebnild/ed, still it watch/es o'er the town As the sum/mer morn was break/mg, on that lof/by tower I stood,/ And the world/ threw off the dark/ness, like the weeds/ of widowhood. Now, it was at one time considered that the three-syllabled unit could never be made the basis for true poetic, work. In the old ballads, in the romance metre of Gower, it gives a beautiful variation to the iambic, but it is only in the degenerate ballads that it predominates. Guest, one of the great writers on English metre, calls it the " tumbling metre," and speaks of it with contempt ; indeed, the three-syllabled unit was, after the date of ballads, avoided by poets generally until Cowper revived it, and in these later days Swinburne and other masters have shown what excellent har- monies it is capable of producing. So it is with the four-syllabled unit : at present, except in isolation, it is outside the pale of true poetry ; but there are indications that it may yet exert as great an influence as the three- syllabled, and produce as distinctive a music. Already it has been used in British poetry for its heightening effect, as the three-syllabled unit was first used, and there is no doubt that it also will produce a type of its own, crude at first, but gradually soaring into true music. It was no doubt the rapidity of the motion produced by the four- syllabled unit that first attracted the Australian writers : poets accustomed to horse-riding, as the popular Australian poets all were and are, preferred a galloping metre ; and, finding one even faster than the three-syllabled, they instinctively adopted and developed it — still retaining the ballad form whilst they modified its internal structure. The following lines from Paterson's " Clancy of the Overflow " give a faint echo of no mean music : — And the bush hath friends to meet him, and their kindly voices greet him In the murmur of the breezes and the river on its bars, And he sees the vision splendid of the sxinlit plains extended, And at night the wondrous glory of the everlasting stars. One fact greatly in favour of the Australian ballad is its breezy joviality and good humour : and what is now contemptuously looked on as mere unpoetic jingling will, I feel sure, prove to be the preliminary tuning-up of a new string to the lyre of Apollo. 422 Transactions. Art. XLIII. — yew Zealand Bird-song. By Johannes C. Andersen. [Bead before the Philosophical Institute oj Canterhury, ith Novemher, 1908.] I SPENT a week in December of last year in the neighbourhood of a clump of thirty or forty acres of native bush near Stony Bay, Little Akaroa ; and as this was my first time of being for any length of time near the bush, I occupied myself in recording the notes of such birds as happened to be there. The most elusive notes I found to be those of the bell-bird (korimako • — Anthornis melanura). I could catch and fix individual notes, but it was some days before I could be sure of their sequence. The reason will be seen on referring to the records following : — &VO. > &va.. (J) -¥M^ <:» (2) ^ rV^JJ^ 8i/a . &ia t-3) (6) iv^ . (t) f 7 f 7 [T'-Tr^^ or 0) ^^ ^^^ [• V k*"' i< I' — V- r^j V \/ i- i*. i i> and so on. The pitch of the initial note of the phrases (1) and (2) varied from d to c, as shown in (3). The consequence was that on checking the notes taken one day with notes taken the next I found they differed, often to a wide degree. I was not able to discover if the variation in pitch was due to the song being sung by different birds, or if one bird was able to vary it as it pleased. The most usual phrase was (1) : the notes follow one another very quickly, the two concluding the phrase being most distinctive and characteristic. A variation where these two notes are discarded is shown in (2). Here the whole phrase is lengthened, and two notes of differ- ent pitch introduced — the two last, which are sustained longer than those preceding. These concluding notes are very pleasing, the last especially being deep, full, and melodious. I only heard this variation as a continu- ation of (1), and then only when the two distinctive notes were discarded. The difference between the day-song and the even-song was very marked : in the latter the notes were sung more deliberately, and, whilst the general theme of the day-song was followed, the intervals were slightly different. The parallel of the more usual day-song was also the more usual even- song (4) : it will be seen that a pause approximately twice the length of the note was made after each note, and the distinctive note uttered only once, the interval between the acciciatura and the main note being also less. The variation of the even-song (5) ended on the same note as the variation of the day-song, I more than once saw a bell-bird on the top of a dead tree at the edge of the bush repeating one or other of the phrases (4) and (5) in Andersen. — New Zealand Bird-song. 423 the evening, at intervals of perhaps half a minute, and for five or more minutes at a time. As twilight deepened a new theme was taken up : the tree-top sentinel disappeared, and from the dark bush came the quickly uttered notes shown in (5). These would be continued, with the slight variations shown occurring now and again, for two and three minutes with- out pause or cessation ; and when they ceased no other note was heard, the next cry coming from the now stirring morepork : his cry consisted of two muffled but clear notes, the second a semitone lower than the first. I heard more of the whirring flight of the tui {Prosthemadera novcB- zealandice) than of his song, the commonest call I heard during the week being a repetition of a single note, from four to eight times, the most frequent number being five, as shown in (1) following : ,, . SfCL ^, Si'a. (1) r ^ r * -^ - — ■ f.-; >^ L ' ■ (3) -Jjl'ITrf zsx hree A/ctu^' hruri: 'Hrurr T It was especially noticeable of the pitch of this note that it never varied : every time I tried it it was h. Fenwick, travelling in the southern part of this island, recorded the note as /, and said that it varied in different locali- ties. The five notes were generally, though not always, followed by the three gutturals hree, hraw, hrurr. These gutturals have no definitive pitch ; each has its distinct vowel sound, however, and they can be imitated by breathing the words rather than articulating them ; the r carries the Ger- man sound, produced by slight vibration of the uvula. The five notes are ventriloquous — that is, they appear to come from a distance away from the bird ; and I, having been told the notes were those of a bell-bird, thought the tui I was w^atching answered them with the gutturals : I soon saw, however, that the same bird produced both. The notes have a clear, mellow tone, and when uttering them the bird sits motionless, with outstretched neck, in some high tree — usually, when I saw him, in a totara or black-pine. The last of the gutturals, hrurr, was at times used as the initial for the slur shown in (2). This high slurred note was very sweet and plaintive — one of the sweetest of all I heard. I heard these calls of the tui much more often than his song. This song (3) is an instance of seeming imitation : the theme is the same as in the song of the bell-bird, the difference being in the intervals and the tempo. The initial note varied almost to the same degree as that of the bell-bird. The two distinctive final notes of the latter, however, I did not hear imitated. In the tui song the fourth and sixth notes, both a, were long-drawn and most melodious. I heard no other notes from the tui : I came too late in the season to hear him at his best. The black fantail (tiwakawaka — Rhipidura fuliginosa) had a slurred note that was similar to the slur of the tui, but was a sixth higher. I heard the fuller song of this bird only once. It alit on the rough bark of a black-pine only a yard " '" from me, and twittered a pleasant little song, of limited range, however, and little variation. I did not wish to interrupt it, as it was the first time of hearing it, so did not take the pitch ; and, unfor- tunately, I did not hear the song a second time. It hovered about the opening-note, never more than a tone (more often a semitone) above or below, being, indeed, hardly more than a twitter. 424 Transactions, I saw only two parrakeets (kakariki — Cyanoramphus novcB-zealandice) during the week, and from them obtained (1) and (2) following : — BvcL... (2) rif m'r The first notes sounded very like the words " Take me back," and were repeated at fairly long intervals. The quality of the parrakeet's note differs considerably from any others that I heard : it could be imitated on an oboe or clarionet ; the tui and bell-bird might be imitated on a mellow flute, though it would be difficult to render the high notes with sufficient softness. The weka {Ocydromus) was fairly common, but I obtained only two calls, as follow : — 9va^. Hi, (I) i"~p'-, fTf'-, i'^r'v (2) i't^- jZ^ The first call was the usual one ; I heard the second only once. These I take to be the call of the female weka ; for, according to an old Maori war- tale, the cry of the female is 'ko-ee, ko-ee, Iv-ee, whilst that of the male is tee-waka, tee-waka. Of all the songs I heard, the most interesting to me was that of the grey- warbler (riroriro — Pseudogerygone igata). In the bush, it was the least developed of the songs that had got beyond a mere twatter, such as that of the fantail — that is, it has not yet acquired a definite succession of phrases, nor is the range of notes at all wide ; but, whilst it is the least developed, it shows great possibilities for varied development. The warbler is one of the native birds commonly found around human habitations ; it may constantly be heard, especially in the morning ; and the peculiar thing is that away from the bush, possibly under the influence of introduced song- birds, the song of the warbler has acquired a certain definiteness. The melody that may be heard almost every morning in any part of Christchurch is shown in (1) : — Sea. StfOi. (1) r^rt (2) PP The phrases always follow in this sequence when the full song is sung. It may break off at any part, or, if continued beyond the notes written, it is an exact repetition." There is, however, a variation that I have heard in the song of the town bird ; the variation is irt the four concluding notes, as shown in (2). Here an enharmonic note is introduced, adding still more to the plaintiveness of the melody. The last note is invariably much lighter than those preceding, and there is a distinct accent on the first note of every phrase of five. Last year, when the variation was introduced, I did not once hear the song continued beyond it : this year I have heard one bird con- tinue it, repeating the variation. The song is very sweet, though so highly pitched. On hearing the variation, one is impressed by the idea that it is a late development, as there is a hesitation in the uttering of the enharmonic note : the interval introduced, too, is wider than usual. Knowing this song, it was with surprise that I heard the very different song of the bush- warbler. The phrase of five notes, the last a semitone below the first four, Andeksen. — New Zealand Bird-sonq. 425 evidently the basic phrase, was constant, but the combination of the variously pitched phrases followed no sequence that I could discover. It meandered on in the way shown below : — Si'o TrrrtrcrrTrtrrr^^r.rTrflTTrcrr^rrprrt There was nothing regular nor determinate : the phrases did not always fall in three sequences, a higher interval following as frequently as a lower : the song, too, was prolonged indefinitely, as if the bird itself had no idea of rounding it off. In the bush I only once had the good fortune to actually see a warbler singing. It was perched on the topmost branchlet of a ribbon- wood at the edge of the bush, which lay below it in a deep valley, and it sat turned towards the trees below, facing, with outstretched neck, now this way, now that, singing like a prima donna to a rapt audience. I have often seen the dilating and throbbing throat of a singing-bird, but in this warbler not only the throat but the skin completely round the neck seemed puffed out with ruffled feathers, and throbbed as the bird sang its long, irregular, indeterminate, minor melody. This was the most tantalizing of the songs : I constantly heard it, faintly as if far away in the bush, and it repeatedly distracted me into endeavouring to catch a sequence in its measures whilst I was taking the pitch of other notes. I was unsuccessful, however, in obtaining any definite sequence beyond the five notes of the basic phrase. The pitch is very high, and I do not know of any instrument by which it could be imitated. Another very highly pitched note was that of what I assume to be a young bush-wren or rifleman (titipounamu — Acanthidositta chloris). It was the only bird of the kind I saw, and it sat on a vine a couple of yards away, uttering the very faint, cheeping notes : — 2 Sua. ggg It was hardly louder than the chirp of a cricket, and though so high in pitch was remarkably sweet and plaintive. There was one bird which I was unable to identify, either on the spot or subsequently, though now I think it may be a hedge-sparrow [Accentor tnodularis). It was a little larger than a sparrow, dark grey, with darker colouring along the upper parts, and tail long and narrow. I saw it singing several times : it clung to a vine, moved its head a little from side to side as it sang, its tail quivering as the note with the tremolo, as shown in the melody below (1), was uttered : — 0,1 q i.'J 1 "^ ri*rr — r L L.>L.J r ,i»,""^" As will be seen, the melody, which is very regular and distinct, is much longer than that of any other of the bush birds ; and this led me to conjee- 426 Transactions. ture that it was not a New-Zealander. The melody was not always sung fully through ; more often it was broken after the first or second tremolo, or after the theme ending on (j flat. Sometimes the two phrases enclosed between single bars would be replaced by the phrase enclosed between double bars ; but I repeatedly heard the full melody as above. On certain days this bird was very plentiful ; and one day, there being but little bird- song, I was trying Schubert's " Fisher-maiden " on my whistle, when no less than four of them perched close beside me piping away most ener- getically, and the louder I whistled the louder and faster they piped, as if they thought it their duty to pipe me down. The pitch varied con- siderably, but, as I doubted the bird's being a native, I was content to take down the melody. A call which the bird sometimes uttered, with no melody preceding or following, is shown in (2). Should this prove to be the song of the Accentor, it would be interesting to know how it compares with the song of the Home bird. Observations will have to be much more extended before any compari- sons can be made or remarks offered on the different songs ; and I have offered these incomplete notes in the hope that others who are in the bush may be induced to record notes in various parts of the Islands, so that com- plete records may be had of the songs of all our birds, in all the months of the year, as well as in all localities. Additional Eecords taken in Decembeb, 1908, from Birds in the. SAME Bush. Bell-bird : The notes were similar to those taken last year. Tui : The following additional notes were obtained : — 8va- 'aL -Xjt^^tjlT^: (4) ^ y q> Y > 1^ z^ tiu tiu aitrr tsrr &va - T »va (8) tiu till aiirr till tiu aurr When uttering the notes a opening (4) the neck was stretched out, with the bill half-open. The sounds represented by tiu tiu aurr were repeated very quickly : the tiu was like the striking together of two hard stones, the aurr being quite different — a decided guttural. The pitch was quite distinctly e and a. These sounds took the place of the hree kraw krurr heard last year. The tsrr was like the sound of a corkscrew being forced through a stiff cork, and it, with the aurr preceding it, was very emphatic. The high, sweet, slurred note following was sometimes succeeded by a very soft, melodious, canary-like phrase, which bubbled, like honey transformed to sound, in the throat of the bird, so softly that it could only be heard at close quarters. I several times heard (4) sung the full length ; more often it broke off after the tsrr, or after the slurred note. The note in (5) was repeated alone. It is " explosive," but very clear and bell-like. It was only sounded once — that is, it was neither preceded Andeksen. — Neio Zealand Bird-sona. 427 nor succeeded by any other note ; and if a cork could be imagined as a clear sound, it was as if the note popped like a cork from a bottle. The notes of (6) were also very bell-like in tone, but were of quite a different nature from (5). They were deliberately sounded, an average of two seconds separating them, the variation (7) was as often heard as "(6). The sounds of (8) are merely part of (4) repeated without any notes : one would suppose they would rasp the bird's throat to pieces. They were varied— /iw tiu aurr, tiu tin tin aiirr, and tiu tiu tin aurr, tiu tiu tiu aurr. Weka : One other call was heard ; it calls for no comment : — 3va. C^) Ar.^/^ ■ /I i^j^^^i "-^^^ Fantail : The following notes were obtained 8va tchi tchi twee twee tu-ee fchrut tchrut twee taee twee The note is not clearly sounded ; it is uttered more as if forced through a constricted passage, and it is rather a twitter than a whistle. It varies not only in pitch, but in sound, so that it may be represented by different letters at different times, as above. Whilst singing, the bird flits restlessly about the bough. Morepork (ruru ; Ninon novce-zealandicB) : — 8^•a^■ (}) JvJvJyJvJvJJ yJ^ The cry is more commonly heard without the five introductory notes. It was muffled, as one might imagine the cry of the hokio, the ominous bird of battle. The Maori represented the latter part of the cry as kia koa, and the sound might well be given as koa, pronounced like caw with a slight vibration of the uvula. Grey-warbler : Two complete songs were obtained : — 28va > > > > > > > > > > > > (S> :tr::T'^ ea'mmar/Ejg^E Za va. - > > (t> ^sr"[L^m'"m'c!r'CQ'm'C£;mE£r > > > > > > C£r"C£.^ It will be noticed that the phrase of five notes is this year replaced by three triplets. The^ falling sequence in semitones is similar to that recorded last year, and again it will be noted that there is nothing determinate in the song. The termination of (3) is effective : I heard it only once. 428 Transactions. Wren : The note of the wren was this year c sharp as against e last year. The only variation, if it can be called variation, was in the suppression or insertion of rests. The notes might be single, or broken into groups of two, three, four, or more, or they might be uttered up to fifteen times with- out a break in the sequence. Kobin (toutouwai ; Miro alhifrons) : This bird's note, a sharp, clear whistle, was of a very simple nature, being a repetition of one note, a sharp. Sz-a,. (I) ^ 44 ^ 3 d .V «J .y Jr =^^^ Yellow-breasted tit (ngiru-ngiru : Petroeca macroccphala) : This song is simple, but very pretty and plaintive. It is a soft twitter, nearer a whistle than the twitter of the fantail, and is uttered during flight as well as when the bird is stationary ; in the latter case the throat and tail quiver slightly. SSt-a (0 r^ r1 M 1^ F^ •' Ufe^ f» — » — ^ O — |»77^K-1 1©- MB~\ ®- B 1 »— ^ B lt —ft — f, •. -f ff y / ^s^^ ^t>. tiu tiu tiveet ti- J— e 't ti u — / — w — / tweet tweeu'eeweewee weet Blight-bird, silver-eye, or wax-eye (tauhou : Zosterops ccerulescens) : Setting aside the rambling melody of the grey-warbler, the blight-bird has the longest definite song of the native birds — so long, indeed, that the name of " tauhou " (the stranger) is justified ; for the songs of the true natives are all short. I heard the song of one bird only, but as it sang away, with slight intervals, for from five to ten minutes, I was able to take- down the various phrases which it employed : — (O The bird was very obliging : whilst it paused it allowed me to take the pitch and intervals of the various notes of the phrases in (1). Whilst it sang it sat quite still, holding its bill in the air ; its throat throbbed, espe- cially when sounding the notes represented by tiu. As in the case of the fantail, most of the notes could be represented by letters. The song was very quiet and sweet, somewhat like that of a canary, but not nearly so shrill nor vigorous. The songster was quite alone : I heard no other blight-birds near at the time. The phrases were employed in all sorts of sequences : there may have been others which I did not catch, for at first I was content to sit still and listen : other individuals, too, may have different phrases. The following combination is an approximate represent- ation of the song ; but, as stated, the combination constantly varied : — ■^St^d- (3) tin tin tiu ti- -/■ — M — f tweet twee wee wee wee weet tin tiu fe=E S I ti — u — eet twee wee wee weeweet tiu tiu tweet Hill. — The Great Wairarapa : A Lost River. 429 Art. XLIV. — The Great Wairarapa : A Lost River. By H. Hill, B.A., F.G.S. [Read before the Hawkers Bay Philosophical Society, July, 1908.] Some time ago, when dealing with the artesian beds forming the Heretaunga Plain, passing reference was made to a large river that at one time flowed through what is now a portion of the ocean, and known as Hawke's Bay. At that time the extent of the river towards the north and west had not been determined, but, as further information has now been obtained, a descrip- tion of the river and the physical changes throughout the district that have taken place since then are here summarised. ooimicc & tianitc-peat areas 20 30 mite^ 39 S. Lat. Fi(i. 1. — East Coast between 38° and 40^ S. before Subsidence. The description will be Umited to the upper portion of the river, from its source as far as the northern end of what is known as the Forty-mile Bush, some miles to the south of the parallel of 40° south latitude. The east coast of this Island from East Cape to Castle Point presents features that imply important physical changes at no distant date. Hawke's Bay water-area is a deep bight, with Portland Island and the Mahia Peninsula at the northern entrance, and Cape Kidnappers at the southern. The bay 430 Transactions. itself, in reality, is a j^ortion of the more inland plain-area tliat has been filled in by the material brought down by rivers such as the present Tuki- tuki, Maraetotara, Ngaruroro, Tutaekuri, and Esk, all of which now flow from the westward, some as far back as the Ruahine Mountains and the Kaweka. The plain known as the Heretaunga Plain is a late formation ; in fact, the process of growth is still going on, and the action of floods on the waters of the bay is such as to bring about a slow sedimentation of the area that was at one time a land-area connected in structure and formation with the hills forming Scinde Island, Napier, and the rocks exposed along the northern and southern ends of the bay. What is here said of the growth and changes connected with Hawke's Bay can also be said of the plain-area hu Wa/'paos. r/yer bas/'n 39° S OJd remains cf shintj/e- ?0 30 miles Fig. 2. — East Coast after Subsidence ; New River-basins. between the mouth of the Wairoa River and Te Kapu or Frasertown, some ten miles inland. So, too, the Poverty Bay plain forms a part of the water- area, and both of them occupy the place once occupied by hills that united Young Nick's Head with the hills that now bound the coast along what is known as the Kaiti side of Poverty Bay. The east coast between East Cape and Cape Turnagain at one time extended much farther seaward. The map marked fig. 1 shows some of Hill. — The Great Watrarapa : A Lost River. 431 the extension. At the time when this condition existed the general slope and river system of the Island were very different from what is now the case. The slope was generally to the east by south, and the Ruahine, Ka- weka, and Titioktira Ranges had not then reached their present elevation. The volcanic district was directly associated in slope and drainage with the east side, and numerous tributary streams carried their burdens of shingle, pumice, and vegetable material from the back inland country, and spread them broadcast over basin-like areas in a river-valley of great length that was in process of making by the slow elevation of what now constitutes the chief axial structure of the Island. Fig. 3. — East Coast, showixg Plain-growth since Subsidence. Shading shows Plain- growth — the Plains filled and fokjied since Subsidence shown on Fig. 2. In order to obtain a clear idea as to the surface features of the country at the time under notice, map fig. 1 should be studied. It shows the probable extension of the coast eastward beyond what can be seen in the dotted lines of the present coast, and the various streams that now constitute different river systems are seen to form one river that had its head-waters in the back country to the westward of Poverty Bay. Out in the ocean to the south-east of Poverty Bay the river made a bend to the south by west, and proceeded past the Mahia, through Hawke Bay, and south- west into the valley now known as the Heretaunga Plain, and thence west by south onward to the Wairarapa. On its course it received from the back 432 Transactions. country a large number of tributary streams, most of them being heavv shingle and pumice carriers. By means of the network of tributaries from the west, the country was bared of a large part of the limestone that covered it at the close of the Pliocene period, being replaced by heavy deposits of shingle and pumice of great thickness, and of a kind that is now character- istic of the country between the Kaimanawa Mountains and Tauranga- Taupo. Towards the close of the Pliocene and the opening of the Pleistocene periods great and important changes took place. Great volcanic activity was experienced in the interior of this Island, and the east coast was shaken to its foundations. It was during this period of activity that a large portion Fig. 4. — East Coast, showing River Systems as at Present. of the coast disappeared and sank beneath the ocean. Hawke Bay, Here- taunga Gulf, Wairoa Gulf, Poverty Bay, and Turanganui Gulf were formed at this time. The Great Wairarapa disappeared as a river, and the entire aspect of the water drainage was modiiied. A reference to map fig. 2 shows the condition of the coast and the physical features of the land following the subsidence and the disappearance of the Great Wairarapa river-basin. What had formerly been tributaries of a great river now began to form separate basins of their own, and we have the interesting fact that by ordi- nary earth-movements new rivers and river systems may be brought into existence and the facies of a country completely changed. Hill. — TJic Great Wairarapa : A Lost River. 433 An inspection of the areas that now form the river-basins shown in map fig. 2 will supply the fullest evidence of a contemporaneous past in the shingle, pumice, sand, and vegetable deposits that are found wdthin them. In Poverty Bay, the Kaiti Hills, the lower hills on the Whataupoko, the hills near Ormond, Te Karaka, and numerous others abound with facts to show the state of the country before the present plain and river-valley were in existence. Similar evidence is forthcoming in the case of the Wairoa, Mohaka, and the other river-basins of Hawke Bay. At the entrance to the Wairoa and Mohaka Rivers, and on the hills towards Frasertown and the Wairoa Hospital, shingle and pumiceous deposits occur, and in the inner portion of Cape Kidnappers, extending from the Black Reef, sections 200 ft. in vertical height display the same characteristic beds such as are met with, ct^^ Fig. 5. — TunAX(iANUi Gulf, after SrBsiDiiNXE. though less developed, in Poverty Bay. To the north-west and south- west of the Kidnappers, through Maraekakaho, and thence past the Gwavas Station on to the Ruataniwha Plains, the hills both to the right and left are made up solely of the Kidnapper and Poverty Bay shingle series, and these continue through Takapau, Ormondville, Matamau, and Dannevirke in varying thickness and extent. All the deposits within the limits of the areas named bear witness to the iact that the supply of materials was from the westward. There was 434 Transactions. a general similarity in tlie physical conditions of the whole district at the time, and the flora and fauna were much like those of to-day. Over the whole area there are usually traces of lignite-beds of varying thickness. These occur along with what appears a pumice-mud deposit. In these beds fossil specimens of leaves occur of many kinds. I have collected more than a hundred kinds in a state of perfect preservation. In the same beds are specimens of fossil fish vertebrates, insects, flowers, and ferns, and a single specimen of a fossil feather. The beds have not been by any means carefully explored, and a rare garnering awaits the young geologist who is anxious to make a collection representing the animal and vegetable life of an interesting period in the geological history of this country. Kidnappers, Whataupoko, and Ormond are the best collecting-grounds at the present time. An inspection of map fig. 2 will show that the rivers which were suddenly brought into independent being had to carve out a destiny for themselves. The country was high, and covered wdth deposits of shingle, limestone, and in some places blue-clay marls. Each river-mouth was miles from where it is now to be found. Denudation was great, and loose material was easily removed seaward, and deposited in the small gulfs and f Ji'i'j'^' ^^"f^'^'^L. Fig. 6. — Cross-section showing Filling-in of Beds. bays along the coast. The Tukituki had to carve out a way for itself, but this took a long while to accomplish, for, with the Makaretu and Waipawa Rivers as helpers, a place had to be worn through the Kmestones at the spots known as the Waipawa Gorge and the Waipukurau Gorge respectively. Lakelets were formed, to be broken through from time to time as the river kept finding its course to the sea. The Ngaruroro and Tukaekuri Rivers began to pour their waters into the area now occupied by the important Heretaunga Plain, which grew at a rapid rate, as soon as the Tukituki began to poiu' its burden of shingle into the bay in the vicinity of the gorge behind Havelock. Map fig. 3 shows the work that has been done by the several rivers since they came into existence, following the great subsidence along the coast. Ruataniwha, Heretaunga, Wairoa, and Poverty Bay Plains have all been formed by means of the materials that the several rivers have carried down in time of flood. Slowly the mouths of the rivers have extended Hill. — TJie Great Wairarapa : A Lost River. 435 seawards as the deltoid areas have grown year by year, and rich lands have taken the place of the once water-area, and the same process of growth is going on to-day. The rivers are still carrying down their treasures of material to the lowlands, and these latter are being aided by man's in- telligence and industry. Since the formation of new drainage-areas and river Tofd! deprh MAKAURI, POVERTY BAY, 3'bore, 3'}7'deep 37' 82' 37' Abundijnce j ot (fas I >/67' Y^oterwith \ Jiftle gos ( '^' 217 \ Water to tcp\ZI8' e ■ \ 22J ' of pipe \224-J Thickness *. characfer of beds /2'j-e//on /cam 26'b/ue sandy c/av 4-5' blue f,pcnqy cloy JS ' blue ^andy c/ay 70' blue tcugh spongy Cloj>. 30' dork pipeclay 20 ' dork gre^cn clay ^1' white pumice. 3 'sand & &ma/l gravel 3' bculdcn i, sandstone •^9' /lord roc A. Fig. 7. — Aktesian-well Section, showing Details of Bedding. systems, as shown in map fig. 2, the " made land " along the coast, as won from the sea, must amount to over 150,000 acres, and carries a population of about forty thousand persons. It would be interesting to know the annual value of the products of the land that has been made by deposition from flooded rivers, but the facts are not available. 436 Transactions. Map fig. 4 sliows the east coast as it is to-day, with the several rivers running into Poverty Bay and Hawke Bay respectively. The plains are not to be distinguished from the other portions of the land-area, for nature heals wounds, and only leaves remnants of a past, after the manner of a camping-ground in the case of Natives or a party of picknickers. In a former paper on " Artesian-water Basins of Heretaunga Plain " (Trans. N.Z. Inst., vol. xxxvii, p. 432), sections are shown to illustrate the growth of the plain, and reference is made to the Great Wairarapa that flowed over the area long before the plain was formed. At that time my inquiries had not extended to Poverty Bay, but the sections (figs. -5, 6, 7, and 8) give in regular sequence the geological events and proofs such as are given in the above paper with respect to the Heretaunga Plain. \T£,tC "kAAA /J/' \HAlt€/fATAHJ S-^ Povertj^Bay 'MVJf/WA/ Young Nicks Hd o I s 3 A 6 miles Fig. 8. — Pkesent Plain-slope and Physical Features. At the time of subsidence a gulf extended inland of the present Poverty Bay even beyond Kaiteratahi, and into this gulf, which is named Tau- ranganui, several important rivers flowed. As in the case of Heretaunga Plain, the rivers were and are great carriers of debris, and the plain as a deltoid changing area has grown in a manner almost identical to that of Heretaunga, so that the work of growing is still in progress. The cross-section (fig. 6) shows the bedding of the present plain from the hills near the school at Te Arai, and the hills over which the road passes to the Waimata. Along the plain is shown the location and depth of artesian wells that have been put down from time to time, and fig. 7 shows a complete section of one such well. The present slope of the Poverty Bay Plain is shown in fig. 8, which gives heights, and river-drainage, and railway-line. Hill. — Dacttjlanthus Taijlori. 437 It is not necessary here to refer in detail to the interesting questions suggested, as my purpose is merely to show how two districts, separated so far apart, when placed side by side illustrate identical conditions in their changes, their growth, and structure. Nature works on similar lines, al- though the final results may be dissimilar ; but here, over a district extending through two degrees of latitude covered by these remarks, the geology can be read without difficulty. Thus the past can easily be dovetailed with the present. Construction and destruction are ever in operation, and all the forces of nature have one of these two ends in view. A whole district like that along the east coast may suddenly disappear, but upon the ruins new foundations at once begin to be built that in the end show sufficient growth as to become suitable as man's dwelling-place. The geologist cannot say how long it will take to fill up the waters that were once land-areas, but the process that immediately followed the disappearance of the Great Wairarapa still continues, and will continue unless there should come another period of volcanic activity and earth-movements such as was experienced at the going-out of the Pliocene and the coming-in of the Pleistocene periods in the geological history of this country. Art. XLV. — On Dactylanthus Taylori. By H. Hill, B.A., F.G.S. [Read before the Hawke's Bay Philosophical Society, \3th August, -1907.] In vol. xxviii of the " Transactions of the New Zealand Institute," p. 493, there is an article by the late T. Kirk, F.L.S., on Dactylanthus Taylori. It contains all the information which was known up to that time concerning the life-history of this interesting and solitary (?) New Zealand genus of the order Balanofhorew, which includes a variety of root-parasites. Kerner and Oliver, in their " Natural History of Plants," vol. i, p. 161, state that " the distinctive property of true parasites resides exclusively in the with- drawal of nutrient substances from the living vegetable or animal bodies which they invade." Based upon this definition, parasites are classed into three groups, the first including " generally all microscopic forms which live in the interior of human beings and animals, chiefly in the blood " ; the second including " fungi possessing mycelia which have the power of withdrawing by the entire surface of their filamentous cells or by clavate outgrowths of the same nutritive material from the tissues of the host in- vaded by them " ; and the third comprising " flowering-plants wherein the seedling upon emerging from the seed penetrates into the host by means of suction roots, or some other part which subserves the function of a suction root, so as to absorb juices from the host." It is to the latter group that Dactylanthus Taylori belongs. The order BalanophorecB contains about forty species, belonging to fourteen genera. They are mostly tropical or subtropical in their distribu- tion over the Old and New Worlds, and are usually found in the deep re- cesses of the forest. 438 _ Transactions. In the first edition of " New Zealand and its Inhabitants," by the Eev. R. Taylor, published in 1855, there appears on page 430 a picture of a new- plant, " fam. BalanophorecB,'" that is evidently intended to represent the Dactylanfhus, but no word is mentioned in the botanical notes about the plant. It may be that Mr. Taylor, at the time when the book was first issued, had merely seen or been shown an imperfect specimen of the plant, as in the second edition, which was issued in 1870, or fifteen years from the time of the first issue. Sir Joseph Hooker's description of the Dactylanthus is given, with several fine illustrations of the plant from specimens supplied by Mr. Taylor. The claim set up by the Rev. Mr. Taylor as the discoverer of the Dacty- lanthus has been recently called in question by the son of the late Mr. Francis Williamson, of Wanganui, who writes as follows : " Dear Sir, — The Dacty- lanthus Taylori was first discovered by the late Francis AVilliamson, of Wanganui, who arrived in the colony in the early forties. It was found at the root of a Pittosporum tree, at a place called Putotara, a property owned by him. The plant was about the size of a large pine-apple ; but, instead of having the top as a pine has, it had five flowerlike stalks, three of which were in bloom, and very sweet-scented. The other two were just buds. My father, being a botanist, knew this to be a new plant, and packed it to send home to England ; however, as he heard the Rev. R. Taylor was about leaving for the Old Country, he took the specimen to him, who promised to do him the favour, and to give all particulars as to who fou.nd it, &c., Mr. Taylor saying it appeared to be quite a new plant. The next my father heard was that the new plant was named Dactylanthus Taylori. — D. H. Williamson, Havelock N., 30/7/07." In Mr. Kirk's paper it is stated that the plant was discovered by the Rev. Richard Taylor, about 1857, growing on the roots of Pittosporum, Fagus, and other trees, at an estimated altitude of 4,000 ft. This may be true as far as Mr. Taylor himself was concerned, as he probably had not seen the plant growing before 1857, although there is a picture of the Dacty- lanthus flower in his work published in 1855. " Pua reinga " is the name by which the plant is said to have been known to the Natives ; but I have never heard it so called, nor do I understand why it should be known as the leaping, or springing, or jimiping flower. When found by me many years ago a Native was with me. The place was Mata- rau, near to Hicks Bay, beyond the East Cape, and the Native without any hesitation called the plant " wae-wae-atua." Since then I have found the plant growing in many localities in the deep recesses of the bush, but whenever seen by Natives the same name has been given, and a very old Native of Taupo — Paul Rokino — gave me an old ivaiata referring to the flower. The name " wae-wae-atua," or the fingers, the foot, or toes of the atua, seems an appropriate one, for the appearance of a number of fru^iting speci- mens, as shown in-Plate XXXI, fig. 1, as they appear above the surface of the ground, generally on the slope of a bank in a deep gully, is curious and strange. Mr. Kirk, in his notes, gives localities where the plant was first discovered by various collectors. The earliest-known specimens were taken from within the basin of the Wanganui River; but Mr. A. Hamilton, Director of the Dominion Museum, was the first to find specimens along the east coast, at Tarawera, and subsequently at Nuhaka. It has not been observed by myself at the latter place, but in the vicinity of the East Cape and Hicks Bay it is fairly common, the parasite being of very large size. At Matarau many specimens collected were as large as a good-sized cabbage, and the Hill. — Dactylantims Taylori. 439 smell of the flowers in bloom was very sweet. It has been found by Mr. Frank Hutchinson at Hawkestone and Patoka, in the Puketitiri country ; and I have found many specimens at Kunanga and Opepe, in the Taupo plateau country. During the past ten years the Dactylanthus has been under fairly close observation by me, and the following notes are the result of inquiries made with living and dead specimens. The specimens in my possession, both wet and dry, are of various sizes. In every instance the rhizome is terminal in respect to the particular portion of the root on which it is found (Plate XXX, fig. 1). Panax and Pittosporum are the only two kinds of trees upon the roots of which it can be stated with certainty that the parasites grow. The ends of the most delicate roots are selected by the parasite. Here a swelling appears, having the appearance of a small wart on the human hand. This is very marked in the smaller specimens, where the host portion can be distinguished from the growing rhizome of the parasite by a smoother surface, a different swelling, and a difference of colour. The swelling at the end of a root host looks as if the tissues had been disturbed and cramped during growth, and near the place of junction the root thickens somewhat, as is clearly shown in Plate XXX, fig. 2. In the latter figure the junction of the rhizome with the host can be seen as flowerlike radiations on the lower part of the rhizome, and by corresponding radiations and depressions at the end of the host root. The latter does not cease to grow after being attacked ; in fact, the root appears to grow stronger near the place of attachment with the rhizome, and this becomes more pronounced in the larger and older specimens. When a fresh rhizome is cut into halves so as to trace the root host, the latter, in large specimens, spreads out fanlike and in cuplike depressions, twisted on the outside, and appearing as if the ends of the root had been subjected to great pressui'e. The depressions or cups are filled mostly with a pithy substance, which, when dry, shrinks and leaves several hollow spaces. On the outside of the terminal roots of the host a similar pithy substance underlies the ordinary bark, and it appears as if the rhizome was fed or nourished in the places indicated. The rhizome in a growing state presents the appearance of a large potato covered over with warts. When cut through there is a bluish-purple line not unlike that seen in the blue potato, formerly in common use by the Maoris along the east coast. It is not difficult to cut, and resembles a Swedish turnip except in colour. The taste is neutral, or perhaps slightly sweetish, and when bitten is crisp but somewhat dry, and leaves behind a slight raspy or acrid taste. As the flesh portion of the rhizome approaches the cortical layer it is covered over with pimple-like growths. These eventu- ally push their way through a mass of cortical layer, and form flowering- shoots over the entire surface of the rhizome. If the tubercular growths which cover a rhizome-like wart be cut across, they show a distinct arrange- ment of parts. First come the scales, then a yellowish-white band made up of strands resembling resin. Within this, but touching the inner portion, are ten or twelve horseshoe-like forms, some of a rich orange colour and others a deep purple ; but they always present one or other of these charac- teristics. If the two ends of a horseshoe were joined loosely so as to bend inwards somewhat, the similarity would be complete. I have cut many of the fresh growing tubercles, and have separated the scales one by one so as to get at the central growing portion. This consists of minute growths, not unUke in appearance one of the ripening flowers of a fig, except that each part is made up of two lip-like growths, one being a little larger than the 440 Traiisactions. other. It would seem that the purple tubercles give rise to the female spadices, and the orange to the male. They certainly present similar ap- pearances to what are seen in the complete flowers. The female peduncle is usually shorter than the male, but each varies in size according to conditions of growth and development. The pistillate flowers surround each spadLx. They are very small, are less numerous below, and increase in number upwards, although fewer seeds mature at the top than below. The flower is of two parts, forming a closely fitting perianth as the ends appear above the ovary, and, like the pistil, are per- manent, and can be seen in the ripened fruit, as illustrated in Plate XXXII, fig. 2. The lower part of the perianth is pale yellow, the upper purple, as are likewise the style and stigma. As the seed ripens the ovary swells somewhat, and when ripe the yellow part has changed to a bluish-green, that passes above into a deep purple. This has reference to the perianth only, for when the covering is removed a tiny nut of a deep-purple colour is seen, and within this nut there occurs a white structu.reless substance like wax. The male or staminate flowers have a peduncle that is similar to that of the female, except that it is larger, as are likewise the scales. As the flower expands the scales are symmetrical, and the whole when fully de- veloped is ringent and not unlike a small dahlia (Plate XXXII, fig. 1). The colour of the surrounding scales varies from a straw-yellow in ths outer whorl to a deep orange with purple stripes in the case of the petal-like scales that surround the spadices. The latter vary in number from 16 to 28. About each spadix staminate flowers wind from left to right. The} are connected with the spadix by short filamentary attachments. Each stami- nate flower is of a yellowish-grey colour, fleshy, and presenting the ap- pearance of a tiny disc, with a deep depression running from top to bottom. The pollen appears to be developed along the margin of the anther, and is abundant. As soon as the spadices are fully developed the scales fall back, and the flower eventually dies down and falls off. The flowering takes place between February and April. Until Easter Monday, 1907, I had not seen a male flower in full bloom. Plate XXXII, fig. 1, shows a male flower just opening. As the development of the flower proceeds the scales droop, and the spadices present a straggling appearance. I have made numerous experiments both with rhizomes and seed, but up to the present time the results have not been satisfactory. EXPLANATION OF PLATES XXX-XXXII. Plate XXX. Fig. L Dactylanthus ; root of host, and parasites forming like small tubers. Fig. 2. Root of host, showing mode of attachment of jiarasite. Plate XXXI. Fig. 1. Dactylanthus flowers growing on a bank. Fig. 2. Flowers (female), showing attachment to root. Plate XXXII. Fig. 1. Male Dactylanthu-i flower unfolding. Fig. 2. Flowers — male, female — and fruit : o, staminate spadix ; b, pistillate spadix ; c, ripe seeds from b. Trans. N.Z. Inst., Vni, XIJ. I'L. XXX, Fig. I. ?eai vm s.6ez Fig. 2. DACTYLANTHUS TAYLORI.- Hill. Face p. 440. Trans. N.Z. Inst., Vol. XLT. Pl. XXXI. Fig. I.- * S.GBO. Fig. 2. DACTYLANTHUS TAYLORI.— Hill. Trans. N.Z. Inst., Vol. XLI. Pr.. XXXII. ^G7^ Fig. I. -1 * *> ^ # Fig. 2. Z67e DACTYLANTHUS TAYLOR!. — Hill. NEW ZEALAND INSTITUTE. V i NEW ZEALAND INSTITUTE ADJOURNED SIXTH ANNUAL MEETING. The adjourned meeting was held in the Dominion Museum, Wellington, on Thursday, 4th February, 1909, at 10.30 a.m. Present : Mr. G. M. Thomson, President (in the chair) ; Mr. A. Hamilton, Mr. M. Chapman, Professor Easterfield, Mr. T. H. Gill, Mr. J. W. Joynt, Mr. W. Wilson, Mr. H. Hill, Mr. E. Tregear, Mr. John Young, Dr. L. Cockayne, Professor W. B. Benham, Mr. R. Speight, and the Secretary (Mr. Thomas King). A letter, dated 29th December, 1908, was received from the Department of Internal Afiairs, notifying the appointment (published in the New Zea- land Gazette of the 23rd December) of Messrs. J. W. Joynt and E. Tregear as members of the Board of Governors of the New Zealand Institute under " The New Zealand Institute Act, 1908." The President welcomed Mr. Speight on taking his seat on the Board for the first time. An apology from Mr. James Stewart for non-attendance was read. The minutes of the last annual meeting were confirmed ; the minutes of the Standing Committee meetings held on the 12th November, the 24th July, the 4th December, 1908, and the 25th January, 1909, were read ; and the minutes of the annual meeting of the 28th January last were read and con- firmed. The Secretary explained the circumstances connected with the telegraphic advices of the postponement of the annual meeting. The explanation was considered satisfactorv. The annual report and annual statement of receipts and expenditure were- then read. The report and statement were as follows : — The fifth annual meeting of the Board of Governors under " The New Zealand Institute Act, 1903," was held in the Dominion Museum, Wellington, on the 30th January, 1908, and was attended by fourteen members. The President, 'Mw G. M. Thomson. F.L.8., F.C.S., was in the chair. It was re^jorted that Messrs. Jolin Young and Augustus Hamilton, the two retiring nominees of the Government, had been reappointed, and that the follomng representa- tives had been elected by the societies affiUated to the Institute : Messrs. D. Petrie and J. Stewart (Auckland Institute) ; Professor T. H. Easterfield and Mr. Martin Chap- man, K.C. (Wellington Philosophical Society) ; Professor Charles Chilton and Dr. C. C. Farr (Philosophical Institute of Canterbury) ; Professor W. B. Benham and Mr. G. M. Thomson (Otago Institute) ; Mr. H. Hill (Hawke's Bay Philosophical Institute) ; Dr. L. Cockayne (Nelson Institute) ; Islx. T. H. Gill (Westland Institute) ; and Mr. Kenneth Wilson (Manawatu Philosophical Society). The following officers were elected for 1909 : President, Mr. G. M. Thomson, F.L.S., F.C.S. ; Hon. Treasurer, Mr. Martin Chapman, K.C. ; Secretary, Mr. Thomas King ; Hon. Editor of Transactions, Mr. G. M. Thomson ; Hon. Librarian, Mr. Augustus Hamilton ; Publications Committee, Professor C. Chilton, Professor W. B. Benham, Dr. C. C. Farr, and the Hon. Editor. The honorary members elected v^ere Dr. L. Diels, of Berlin ; the Rev. T. R. R. Steb- bing, F.R.S., of Tunbridge Wells ; and Mi'. E. Meyrick, B.A., F.R.S., of ^Marlborough College, Wilts. There are now twenty-nine honorary members on the roU, and the meeting will therefore be asked to elect one new member. 444 New Zealand Institute. In accordance with resolutions passed at last annual meeting, Professor T. W. E. David, Professor W. A. Haswell, and Mr. J. H. Maiden, all of Sydney, were asked to act as a committee to suggest a suitable recipient of the Hutton Memorial Medal. The two last-mentioned gentlemen have consented to act, but no reply has yet been received from Professor David, who is absent in the far south as a member of the " Nimrod " Antarctic Expedition. The dies for the medal, and several specimens of the medal, have been received from England, and (by permission) have been lodged by the Secre- tary in the Dominion Museum for safe keeping. The Committee set up at last annual meeting " to examine the books of the library with a view to determining their ownership" has never met, two of the members being resident in the South Island ; consequently the position remains unaltered. The same committee was set up to revise the exchange list ; and Professors Benham and Chilton submitted suggestions to Mr. A. Hamilton, the Wellington member of the committee, as to the alterations required in the list. The matter is dealt with in the report of the Hon. Librarian, presented at this meeting. At the last meeting a committee was set up to go into the matter of the delay in the issue of the 39th volume of the Transactions. This committee interviewed the Hon. J. A. Millar. Minister in charge of the Printing Department, and the Government Printer, and obtained a promise from those gentlemen that steps would be taken to expedite the issue of future volumes. The delay in the pe.st year was in part attributed to the unprepared manner in which papers intended.' for publication were sent in ; and the Government Printer undertook to supply a memorandum on the subject for the guidance of Secretaries of affiliated societies and of authors of papers. This memorandum was received by the Editor in February last, and copies were forwarded to the Secre- taries of the several affiliated societies. It is, however, evident that the delay was largely due to the block of parliamentary business ; and to obviate this in future it is advisable that the volume should be printed as early in the year as possible. The committee appointed to make arrangements for the preparation of an index to the forty volumes of the Transac^tions has not been able to come to a final decision as to the course to be pursued. The committee has obt?*ined specifications from two persons cpialified to undertake the work, and is in communication with a third, b\it so far is unable to report definitely. A geographical difficulty similar to the one spoken of in the paragraph referring to the Ownership of Books Committee has prevented the Hector Memorial Committee of the Institute from meeting. The members of the committee live in different parts of the Dominion, and have not found it jn-acticable to assemble in Wellington. They are, however, co-operating with the main Hector Memorial Committee, which has the matter in hand. That committee has been reconstituted, and is in corres])ondence with the other bodies which are acting in the interests of the movement. The amount so far collected by the committees is, unfortunately, too sma-U for the end in view. The main Hector Memorial Committee, at the instance of the Standing Committee of the Board of Governors, has therefore suggested to the Memorial Committee of the Institute, and to the allied committees in Auckland, Wellington, C"hristchurch, and Dunedin, that a joint circular should be issued, signed by representatives of all the committees, appeal- ing for further subscriptions to the fund. This suggestion has been adopted. A draft circular has been drawn up by the main Memorial Committee and submitted to the other committees, and its terms are now being discussed. Members of the Christchurch and Dunedin comnxittces have stipulated for one or two fundamental changes in the wording of the circular. This has temporarily delayed matters ; but it is hoped that agreement will shortly be arrived at upon the points at issue, and that as soon as the circtdar is ready for distribution all the committees will make a vigorous effort to raise a STim of money sufficient for the establishment of a worthy memorial. The volumes of the Transactions remaining on hand are — Vol. I (second edition), 313 ; Vol. V. 30 ; Vol. VI, 21 ; Vol. VII. 143 ; Vol. IX, 214 ; Vol. X, 138 ; Vol. XI, 392 ; Vol. XII. 305 ; Vol. XIII, 142 ; Vol. XIV, 107 : Vol. XV, 280 ; Vol. XVI. 270 ; Vol. XVII. 530 ; Vol. XVIII. 308 ; Vol. XIX, 555 ; Vol. XX, 450 ; Vol. XXI. 454 • Vol. XXII. 560 ; Vol. XXIII, 570 ; Vol. XXIV. 670 ; Vol. XXV. 626 ; Vol. XXVI, 613 ; Vol. XXVII, 605 ; Vol. XXVIII, 688 ; Vol. XXIX. 591 ; Vol. XXX, 684 ; Vol. XXXI, 695; Vol. XXXII 517; Vol. XXXIII. 611; Vol. XXXIV, 563; Vol. XXXV. 525 ; Vol. XXXVI, 686 ; Vol. XXXVII. 604 : Vol. XXXVIII. 750 : Vol. XXXIX, 192 ; Vol. XL, 91. The advance copies of the new volume (XL, 1907) were not received from the printers until the first week of September, 1908, and the main supplies were not available for distribution until towards the end of that month. The volume contains 608 and xvi pages, and 34 ]>lates. The contents of the last two volumes are compared as follows : — New Zealand Institute. 445 JVIiscell.aneous Zoology Botany Geology Chemistry Proceedings . Ajipendix Vol. XXXIX Vol. XL (1906). Pages. .. 76 (1907). Pages. 185 .. 210 124 . . 189 126 . . 47 95 .. Nil 10 .. 31 44 .. 23 24 576 608 Copies of Vol. XL were presented to Parliament on the 8th September, 1908. In accordance with resolutions passed at the last annual meeting, the volumes of the Transactions now stored in the vault of Parliament Buildings have been insured for the sum of £500, and the Institute's books stored in the Dominion Museum. Wel- lington, have been insured for £2,000. As decided at last annual meeting, the Standing Committee has given consideration to the question of reprinting papers which have appeared in the Transactions. After going carefully into the subject, the committee has come to the conclusion that it is not desirable for the Board in the meantime to undertake the reprinting of papers. A question which has engaged the attention of the Standing Committee, and which seems deserving of consideration by the Board as a whole, is that of the constitution of the committees which are sometimes appointed by the Board for the conduct of special business. Several such committees were set up at last annual meeting. These were composed of members residing in widely separated districts of the colony, but in no instance was a convener or an executive officer a^jpointed. The result has been unsatis- factory. Each member of a committee has been in doubt as to who was to take the initiative, and in consequence great difficulty has been experienced by the committees in getting to work. The Standing Committee has found it impracticable to make the arrangements necessary for holding, in terms of the resolution passed at the last annual meeting, a special general meeting of the members of the Institute on the 29th January. 1909, and, in consequence, the meeting in question must lapse. It seems advisable that the practice of granting diplomas of membership to gentle- men who are elected honorary members of the Institute should be revived. Such diplomas were regularly issued under the original Act, and were appreciated by the recipients ; but the passing of the Act of 1903 rendered the wording of the old form of clii)loma obsolete, and no diplomas have been given during the past five years. With a few unimportant alterations the ])hraseology of the old form could be adapted to present-day requirements, and the siipply of amended forms coidd be printed for a triffing sum. On the 16th December. 1908, the Philosophical Institute of Canterbury gave notice that Professor Charles Chilton had resigned his seat on the Board, and that Mr. R. Speight, of Christchurch, had been elected in his place to represent the Christchurch society. The Secretary, Mr. Thomas King, has explained to the Standing Committee that he finds that the secretarial work takes up very much more time than he anticipated, or than he can spare, and that he has therefore, with regi-et, decided not to seek re-elec- tion. The amount standing at the credit of the Carter Bequest Fund with the Public Trustee on the 31st December, 1908, including interest accrued to the 31st December, 1908, was £2,735 16s. 5d. The Public Trustee also holds on account of the bequest scrip in the New Zealand Loan and Mercantile Agency Company (Limited) of the total face value of £32 5s. 5d. His certificate accompanies the present report. At the last annual meeting it was decided that the Hon. Treasurer should be asked to endeavour to arrange with the Public Trustee for the payment of interest on this money at 4i per cent., instead of 4 per cent, per annum. On inquir}', however, the Treasurer ascertained that as a matter of fact 41 per cent, was being allowed on the deposit, that being the rate paid by the Public Trust Office on sums not exceeding £3,000. There was there- fore no occasion for the Treasurer to take action. A duly audited statement of the Institute's receipts and expenditure for the past year, showing a credit balance of £392 10s. lid., is presented with this report. Geo. M. Thomson, President. 446 New Zealand Institute. 1908. Jan. 31 April 14 May 5 Sept. 2 1J 12 91 26 Oct. 15 Nov. 5 »» 18 »j 24 Dec. 15 1909. Jan. 7 ?9 14 ?? 27 1908. Feb. 13 Mar. 14 Mar. 31. April 29. July 2. ,. 25. Sept. 30. Dec. 10. 15. 1909. Jan. 26. Balance in bank . . Petty cash balance Plus credit not \r\ bank-book Less unpresented cheques Balance . . £ 820 0 >Statement of Receipts and Expenditure Receipts. Balance brought forward . . W. Wesley and Sons, Transactions . . A. Bathgate, Maori Art Champtaloux and Cooper, Transactions ., Maori Art Friedlander and Sons, Transactions . . Contribution by Wellington Philosophical Society G. E. Stechert and Co., Transactions Lieut. -Colonel Gaskell, Maori Art and posting A. H. Turnbull, Transactions Whitcombe and Tombs, Transactions C4overnment gi-ant W. Wesley and Sons, Transactions . . Friedlander and Sons, Transactions . . Transactions Expenditure Petty cash. Secretary W. Benham, travelling-expenses Dr. Chilton, ,, James Stewart, H. Hill, K. Wilson, ,, C. Coleridge Farr, G. M. Tliomson, Hotel Cecil Whitcombe and Tombs W. A. McKay, services D. Petrie, travelling-expenses Bank charge G. M. Tliomson, petty cash Whitcombe and Tombs L., L., and G. Insurance Company Miss Millais, services Colonial Carrying Company New Zealand Express Company Government Printer C. Freyberg, services Secretary, petty cash Bank charge Petty cash. Secretary Chapman and Tripp, law-costs W. Chalmers New Zealand Express Company Whitcombe and Tombs C4overnment Printer W. A. McKay, services T. King, Secretary C. Freyberg, services Balance £ s. d. . 361 5 11 0 16 10 4 5 0 0 16 10 3 7 0 5 17 5 ty 16 9 0 0 15 10 8 14 0 1 1 0 0 16 9 . 500 0 0 0 16 10 0 16 9 0 16 9 £906 15 11 £ s. d. 2 0 0 4 0 10 2 7 0 9 13 S 2 9 8 1 0 4 2 7 0 4 0 10 0 15 0 1 3 3 1 1 0 5 4 10 0 5 0 . 5 0 0 5 0 0 1 2 0 9 0 0 3 0 0 0 19 11 0 12 0 0 15 0 5 0 0 9 19 0 0 5 0 0 7 0 2 0 0 . .10 0 1 13 0 2 9 2 1 0 6 . 388 13 0 5 0 0 25 0 0 10 0 0 . 392 10 11 3. d. £ s. d. 6 2 1 0 820 7 2 0 16 9 £821 3 11 428 13 0 £392 10 11 £906 15 11 4" g d. 9 ,735 16 5 32 5 5 £2. 768 1 10 New Zealand Institute. 447 Carter Bequest. Balance, Ist February, 1908 . . . . . . . . . . 2,617 11 10 Interest accrued to 31st December, 1908 .. .. .. .. 118 4 7 Scrip, New Zealand Loan and Mercantile Agency Comimnv. 1st February. 1908 . . . . . . . . . . . . ' . . .\ 17 0 0 Scrip, ditto . . . . . . . . . . . . . . 15 5 5 £2,768 1 10 Invested by Public Trustee, 31st December, 1908 Scrip in hands of Public Trustee Martin Chapman. Treasurer. Examined and found correct. — J. K. Warburton, Controller and Auditor-General. Mr. Thomson moved, and Mr. Hamilton seconded, " That the President's report be received." Carried. Mr. Chapman moved, and Mr. Hamilton seconded, " That the state- ment of receipts and expenditure be adopted." Carried. The Public Trustee's certificate as to the state of the Carter Fund was read. The report of the Editor and Publications Committee was read as follows : — I have to report that the Publications Committee met on the 31st January, 1908, and ■considered the papers which had been handed over to them by Mr. Hamilton, late Editor. Forty-two papers were passed for printing in Vol. XL, and these were at once for- warded to tlie Government Printer, while seven were included in the Proceedings of the societies which forwarded them. Seven were sent to experts to be reported on as to their suitability for publication, and seven were held over. Of the papers sent to experts, six were reported on favourably and sent to the Government Printer, while one was considered unsuitable. In this connection I would point out that the work of the Editor would be simplified if the Council and Secretaries of the affiliated societies would only forward such papers as are considered to be real contributions to scientific knowledge. All papers which are only resumes or digests of already published work should not be sent forward, and the onus of withholding tbem should rest on the society with which they originate, and should not be placed on the Editor. The committee received from the Government Printer on the 10th February a number of suggestions and recommendations, including memoranda from the Super- visor and the Chief Draughtsman. The chief of these were embodied in a memorandum for authors of papers sent out by me to the Secretaries of the affiliated societies. It is hoped that attention will be paid to the details therein specified, as both time and money will be saved thereby. In accordance with the resolution of the last annual meeting, that the 41st volume be the first of a new series, the Publications Committee has gone carefully into the matter, and has come to the conclusions — (1) That the new series should be issued in royal 8vo. size ; and (2) that both Transactions and Proceedings should be of the same size. In the case of any large monographs which it is considered desirable to issue separately, it is recommended that they be printed of the same size as the " Bulletin of the Geo- logical Survey.'- ^^^^ jj Thomson, Editor. ~^ Mr. Thomson moved, and Mr. Chapman seconded, " That the report of the Editor and Publications Committee be received." Carried. Professor Benham moved, and Mr. Speight seconded, " That in future the volumes of the Transactions be published Ln royal 8vo. size." Carried. 448 New Zealand Institute. The Hon. Librarian's report was then read, as follows : — The Honorary Librarian reports that the number of pieces received during the year as exclianges and presentations amounts to 923. No binding has beeir done during the year, and I desire to point out tliat there is still a large amount of binding that requires attention. As mentioned in my last report, the present arrangement of the books is perhaps the most inconvenient that could be suggested, and it would be a great improvement if a sum of money could be provided for modern iron bookcases, to be arranged in bays. I have again to report that very little use has been made of the library, the number of entries made by those taking out books being only forty-six, the majority of these being periodicals and magazines taken out by members of the local society ; in fact, a large number of the books have been taken out by a person who is not a member of the Institute, but who has permission to use the library. I think to a large extent the fact that the library is not much used is owing to the compa,rative inaccessibility of the books. No progress has been made with regard to the card catalogue, as no funds are avail- able at present for an assistant. The stock of Transactions acciimulated during the last three years has been trans- ferred to the cellars of the Parliamentary Library. I have had a typewritten catalogue prepared of the books belonging to the Philo- sophical Society. You will have before you a communication from the Mines, Depart- ment relating to the geological works now in the collection. A separate stamp has been prepared for the books belonging to the Dominion Museum, and for the future a separate binding of brown buckram will be used for the Museum books. A set of pigeon-holes has been provided for the better keeping of the current parts of the various works, and I also had an estimate prepared for a series of shelves and pigeon-holes for the whole of the parts which are received from time to time. The cost, however, was about £60. If funds can be found for this purpose, it would probably insure the better custody of the parts which arrive from time to time. Re exchanges : I have wi'itten to the members of the Committee of the Exchanges,, and have communications from them on this matter. I have, however, been unable as yet to draft a report, as a number of matters have to be gone into first, which cannot conveniently be proceeded with until the alterations in the library now contemplated are decided on. I think it is desirable that a small vote should be made for the purpose of carrying on a certain amount of card cataloguing and classification. I propose to ask tlie Stand- ing Committee to authorise the expenditure of a small amount on further work on the catalogue. 4 Hamilton, Librarian. Mr. Hamilton moved, and Mr. Chapman seconded, " That the Librarian's report be received." Carried. Mr. A. Hamilton moved, and Professor Benham seconded, " That as soon as possible in each year complete copies of the Transactions shall be, in accordance with the Act, presented to Parliament, and that all other copies shall bear that date as the date of issue, and that this date shall be the ' date of publication for the purposes of determining priority of discovery.' " Carried, Professor Easterfield dissenting. Professor Benham moved, and Mr. R. Speight seconded, " That the Editor be authorised to publish the Proceedings of the affiliated societies at intervals throughout the year, independently of the Transactions, and separately paged." Carried. Professor Benham moved, and Mr, Chapman seconded, " That the Lidex Committee be reappointed, substituting the name of Mr. E. Speight for that of Dr. Chilton, and adding that of Mr. A. Hamilton as convener." Carried. Mr. R. Speight moved, and Professor Easterfield seconded, " That the Index Committee consider the question of preparing an index to the volumes of the new series, as issued." Carried. New Zealand Institute. 449' Carter Bequest.— A legal opinion (dated 7th December) from Mr. M. Chapman, K.C., was then read. Mr. Hill moved, and Mr. Gill seconded, " That the legal opinion of Mr. Chapman with, reference to the expenditure of certain moneys under the Carter bequest be forwarded to the Victoria College Council for their infor- mation." Diploma of Honorary Membership. — Mr. Chapman moved, and Mr. Hamilton seconded, " That the form of diploma settled by Mr. Chapman be adopted as the form of certificate of honorary membership." Carried. Mr. Hamilton moved, and Mr. Chapman seconded, " That the honorary members elected since 1903 be furnished with diplomas, and that diplomas be sent in future to all honorary members elected." Carried. Formation of Special Committees. — This matter was discussed by the Board, and it was considered that in future, when Committees are set up, proper provision should be made for the members of such Committees con- ferring \vith one another. Mr. Hamilton moved, and Professor Easterfield seconded, " That all committees appointed shall furnish in a formal report to the annual meeting an account of their year's work." Carried. Hutton Memorial Fund. — Mr. Chapman moved, and Mr. Gill seconded, " That the seal of the Institute be affixed to the ' Hutton Memorial Deed of Declaration of Trust,' and that the seal be affixed by the Presi- dent, who shall sign the deed in the presence of the Secretary as witness." Carried. General Correspondence. — (1.) University of Missouri, dated the 21st July, 1908, asking that volumes of the Institute on exchange account preceding Vol. XXXVI, 1904, be sent to them. Mr. Hill moved, and Mr. Wilson seconded, " That the application of the Missouri University be approved." Carried (the Librarian to decide what volumes shall be sent). (2.) Entomological Society of Russia, dated the 5th September, 1908, requesting that the entomological publications of the New Zealand Insti- tute be sent in exchange for their edition of the " Revue Russe d'Entomo- logie." Mr. Hamilton moved, and Professor Easterfield seconded, " That, as there are no separate copies of the entomological papers, we are unable to grant the request of the Societe Entomologique de Russe." Carried. (3.) Zoological Institute of the Royal University of Naples (no date), proposing the exchange of their " Annuario del Museo Zoologico " for the Transactions of the Institute. Professor Benham moved, and Dr. Cockayne seconded, " That in future the Zoological Institute of the Royal University of Naples be added to the list of exchanges (back numbers. Vols. I and II, to be obtained, and the cor- responding numbers of the Transactions to be forwarded)." Carried. (4.) United States Department of Agriculture, dated the 25th Novem- ber, 1908, asking for back volumes of the Transactions. Professor Easterfield moved, and Mr. Gill seconded, " That the United States Department of Agriculture library be informed that the New Zea- land Institute will supply such of the specified volumes as are in stock for the sum of £10 — a slight advance on the cost of publication." Carried. 15— Trans. 450 New Zealand Institute. (5.) Bureau of Science, Manila, dated the 10th November, 1908, sug- gesting an exchange of the Transactions. Mr. Hamilton moved, and Mr. Chapman seconded, " That the Manila Bureau of Science be communicated with, and arrangements made for an exchange of publications." Carried. (6.) Westport Free Library, Westport, dated the 13th January, 1909, applying for free copies of the Transactions. It was resolved that the request be granted, (7.) Mines Department, Wellington, dated the 27tli January, 1909, asking that the books in the Institute library relating to geology be handed over to the Mines Department, for the purpose of being placed in the Geo- logical Survey library. Mr. Hill moved, and Mr. Young seconded, " That the Institute is unable to accede to the application of the Mines Department for the transference of the geological works in the reference library to the Geological Survey reference library," Carried. (8.) A letter from Mr. Thomas King, resigning the secretaryship of the Institute, was read. Mr. Hamilton moved, and Mr. Thomson seconded, " That the resigna- tion of Mr. Thomas King as Secretary be accepted, and that the thanks of the Council be given to him for his services as Secretary, and it regrets that he cannot continue to act in that capacity." Carried. Mr, Hamilton moved, and Professor Easterfield seconded, " That a certain number — say, ten — of separate copies of papers be printed for the Institute, in addition to the copies supplied to the author," Carried, Election of Officers. — The following officers for 1909 were elected : Presi- dent— Mr. A. Hamilton; Hon. Treasurer — Mr. Martin Chapman, K.C. ; Secretary— Mr. B. C. Aston ; Hon. Editor— Mr. G. M. Thomson ; Hon. Librarian — Mr. A, Hamilton ; Publications Committee^Professor Benham, Dr. C. C. Farr, Mr, R, Speight, and Mr. Thomson (Editor). Mr, Chapman moved, and Mr. Thomson seconded, " That the President be ex officio a member of all committees," Carried, Election of Honorary Member. — The meeting then proceeded to elect an honorary member to the vacancy : Proposed by the Philosophical Institute of Canterbury, Dr, Chree ; proposed by the WelUngton Philosophical Society, Sir George Howard Darwin ; proposed by the Otago Institute, Sir Archibald Geikie, Sir George Darwin was elected. Travelling-expenses. — Mr. Chapman moved, and Mr. Hamilton seconded, " That the travelling-expenses of members be paid as before, and that the travelling-expenses of members attending on the 28th January be also paid." Carried. Mr. Hill moved, and Mr. Speight seconded, " That the Comicil of the New Zealand Institute heartily congratulate Professor Ernest Rutherford on his selection as one of those w^ho have been deemed worthy of receiving the Nobel Prize, and that a copy of this resolution be forwarded to Professor Rutherford, Manchester." Carried. Mr. Speight moved, and Mr. Gill seconded, " That the Editor be the convener of the Publications Committee." Carried. Mr. Hamilton moved, and Mr. Chapman seconded, " That the annual meeting for 1910 be fixed for Thursday, the 27th January." Carried. New Zealand Institute. 451 Mr. Chapman moved, and Mr. Gill seconded, " That the annual meeting for 1910 be held in Wellington." Carried. (An amendment moved by Professor Benliam, and seconded by Dr. Cockayne, " That the next meeting be held in Christchurch," was lost.) Mr. Hill moved, and Mr. Young seconded, " That a hearty vote of thanks \)Q accorded to the retiring President for the efficient manner in which he has conducted the business of the Institute during his presidency." Carried. Professor Benham moved, and Dr. Cockayne seconded, " That the minutes of this annual meeting be included in the 41st volume of the Trans- actions." Carried. The rough minutes of this meeting were then read and confirmed, on the understanding that the Secretary may make such verbal corrections as may seem to him necessary. Geo. M. Thomson, Chairman. APPENDIX NEW ZEALAND INSTITUTE. HONOEARY MEMBEES. 1870. FiNSCH, Otto, Ph.D., Leiden, Holland. Hooker, Sir J. D., G.C.S.I., C. ., M.D., F.R.S., Royal Gardens, Kew. 1873. GtJNTHER, A., M.D., M.A., Ph.D., P.R.S., Litchfield Road, Kew Gardens, Surrey. 1875. ScLATER, Philip Lutley, M.A., Ph.D., F.R.S., Zoological Society, London, 1876. Berggren, Dr. S., Lund, Sweden. 1877. Sharp, Dr. D., University Museum. Cambridge. 1885. Sharp, Richard Bowdler, M.A., P.L.S., British Museum (Natural History), London. Wallace, A. R., F.L.S., Broadstone, Wimborne, England. 1890. Nordstedt, Professor Otto, Ph.D., Uni- versity of Lund, Sweden. Liversidge, Professor A., M.A., F.R.S., Sydney. 1891. GooDALE, Professor G. L., M.D., LL.D., Harvard University, Massachusetts, U.S.A. 1894. Dyer, Sir W. T. Thiselton, K.C.M.G., I Codrington, Rev. R. H., D.D., Wadhurst C.I.E., LL.D., M.A., F.R.S., Royal Rectory, Sussex, England. Gardens, Kew. | 1896. Lydekker, Richard, B.A., F.R.S., British Museum, South Kensington. 1900. AvEBURY, Lord, P.C, F.R.S., High Elms, Farnborough, Kent. Massee, George, F.L.S., F.R.M.S., Royal Botanic Gardens, Kew. 1901. Eve, H. W., M.A., 37 Gordon Square, London. GoEBEL, Dr. Carl, University of Munich. 456 Appendix. 1902. Sars, Professor G. 0., University of Christiania, Norway. 1903. Klotz, Professor Otto J., 437 Albert Street, Ottawa, Canada. 1904. Rutherford, Professor E. F.R.S., McGill I David, Professor T. Edgeworth, P.R.S., University, Canada. Sydney University, N.S.W. 1906. Beddard, F. E., F.R.S., Zoological Society, London. Milne, J., F.R.S., Isle of Wight, England. Brady, G. S., F.R.S., University of Dur- ham, England. 1907. Dendy, Dr., F.R.S., University College, London. Diels, L., Ph.D., Berlin. Meyrick, E., B.A., F.R.S., Marlborough College, England. Stebbing, Rev. T. R. R., F.R.S., Tun- bridge Wells, England. 1909. Darwin, Sir George, F.R.S., Cambridge. Boll of Members. 457 ORDINARY MEMBERS. WELLINGTON PHILOSOPHICAL SOCIETY. [* Honorary and life members.] Adams, C. E., B.Sc. Adams, C. W. Atkinson, Esmond H. Barraud, W. F. Beetham, W. H., Masterton Bell, B. D. , Bell, H. D., K.C. . Bell, Dr. J. M. Blair, J. R. Brandon, A. de B. Campbell, J. P. Chapman, Martin, K.C. Christie, Mrs. Cordelia Chudleigh, E. R., Chatham Islands Cockayne, A. H. Crawford, Alex. D. Denton, George Downes, Thomas William, Wanga- nui Dvmock. E. R. Easterfield, Professor T. H., M.A., - Ph.D. Ewen, Charles A. Ferguson, W., M.Inst.C.E. Field, H. C, Aramoho, Wanganui FitzGerald, Gerald, A. M.Inst.C.E. Fleming, T. R. Fletcher, Rev. H. J., Taupo Eraser, Hon. F. H., M.L.C. Freeman, H. J. Frevberg, Cuthbert Gifford, A. C. Gill, Thomas H., M.A. Gray, William Hadfield, E. F. Hamilton, Augustus* Hanify, H. P. Harding, R. Coupland Hastie, Miss J. A., London* Hector, Charles Monro, M.D. Hogben, G., M.A. Holmes, R. L., F.R.Met.Soc, Bua, Fiji* Hudson, G. V., F.E.S. Hunter, Thomas A. Hurley, G. A. Hustwick, T. H. Izard, Dr. Arnold W. James, Herbert L. Johnson, Hon. G. Randall* Joseph, Joseph Joynt, J. W., M.A, King, Thomas Kiugsley, R. I., Nelson Kirk, Professor H. B., M.A. Kirk, Thomas W., F.L.S. Krull, F. A., Wanganui Lewis, John H., Broken River, Canterbury Liffiton, E. N., Wanganui Litchfield, Alfred H., Blenheim Lomax, Major H. A., Aramoho, Wanganui Ludford, Ernest J. MacDougall, Alexander Maclaurin, Dr. J. S., F.C.S. McKay, Alexander, F.G.S. McLeod, H. N. Marriner, George, Wanganui Mason, Mrs. Kate Maxwell, J. P., M.Inst.C.E. Mestayer, R. L., M.Inst.C.E. Moore, George, Eparaima, Master- ton Moorhouse, W. H. Sefton Morison, C. B. Murdoch, R., Wanganui Newman, Alfred K., M.B., M.R.C.P. Orr, Robert Patterson, Hugh, Horopito Pearce, Arthur E. Petherick, E. W. Phillips, Coleman, Carterton Phipson, Percy B. Picken, Professor D. K., M.A. Pollen, Hugh Pomare, Dr. M. Powles, Charles P. Poynton, J. W. Reid, Frank Reid, W. S. Richmond, Professor M. W. Roy, R. B., Taita* Skinner, H. D. Stewart, John T., Wanganui Stuckey, F. G. A., B.A.' 458 Appendix. Sunley, E. M. Swan, W. G. Collington Tennant, J. S. Thompson, John Tripe, Joseph A. Turnbull, Alexander H. Turnbull, John Ure Vickerman, Hugh WaUis, Et. Eev. Dr. Frederic, Bishop of Welhngton Wilton, G. W. Woodhouse, Alfred James, London AUCKLAND INSTITUTE. [* Honorary and life members.] Aickin, G. Aldis, M. Allsop, G. W. Arnold, C. Aiibin, E. D., M.B. Bagnall, L. J. Ball, W. T. Bankart, A. S. Bartley, E. Bates, T. L., Newcastle, N.S.W.* Batger, J. Beere, D. M., Melbourne Benjamin, E. E. Best, Elsdon, Euatoki Birks, L., C.E., Eotorua Brett, H. Briffault, E., M.B. Broun, Major T. Brown, E. C, Taumarunui Brown, Professor F. D. Buchanan, J. Buddie, J. H. Buddie, T. Burgess, E. W. Burnside, W. Burton, Colonel." Bush, W. E., C.E. Buttle, J. Cameron, E. Campbell, Sir J. L., M.D.- Carr, E. A. Casey, M. Cheal, P. E. Cheeseman, T. F., F.L.S. Ching, T. Clark, A. Clark, A., M.B. Clark, H. C. Clark, M. A. Clarke, E., Wellington Coates, T., Orakei Cochrane, W. S. Combes, F. H. Cooper, C. Cooper, Mr. Justice, Wellington Cottrell, A. J. Cousins, H. G. Cozens, G. Craig, J. J. Crosher, J. Cuff, J. C. Darby, P. De Clive Lowe, G. T. H., L.E.C.P. Devereux, H. B., Waihi Devore, A. E. T. Douglas, W. S. Duthie, D. W. Earl, F. Edson, J. Egerton, Professor C. W. Ewington, F. G. Florance, E. S., Eussell Fowlds, Hon. G., M.P.* Fox, Eev. E. E., Norfolk Island Garrard, C. W. George, G. Gibb, E. Gilbert, T. Girdler, Dr. Goldie, D. Gordon, H. A. Gorrie, W. Grant, Miss J. Gray, S. Griffin, Miss E. M. Guinness, W., M.D. Haines, H., F.E.C.S. Hamer, W. H., C.E. Hansen, P. M. Hardie, J. Haszard, H. D. M. Hazard, N. H. Heaton, F. Herbert, T. Holl of Members. 459 Hodgson, J. Horton, H. Houghton, C. V. Howden, J. Hutchinson, G. Inglis, E. T., M.B. Jarman, Professor A. Johnson, H. D., Te Aroha Jones, H. W., Papakura Kenderdine, J. Kidd, A., M.P. Kirker, J. Kronfeld, G. Lamb, C. E., M.A. Langguth, E. Lennox, J. M. Lennox, N. G. Leys, T. W. Lundon, J. E. McDowell, W. C. McLachlan, J. M. McLean, M. McMillan, C.C. Mahoney, T. Mair, Captain G., Eotorua Mair, Major W. G. Mair, S. A. E., Hunterville Martin, J., F.G.S. Metcalfe, H. H., M.LC.E. Miller, E. V. Milnes, H. A. E. Mitchelson, Hon. E. Moody, T. P., Hikurangi Morgan, H. H. Morton, H. B. Moss, E. G. B. Munro, G. C., Euatangata Murdoch, D. L. Myers, A. M. Nathan, N. A. Newton, G. M. Nicholson, O. Pabst, Dr. Paris, Eev. P. E., Invercargill Partridge, H. E. Patterson, G. W. S. Peacock, T. Petrie, D., F.L.S. Philcox, W. Philson, W. W. Pond, J. A. Powell, F. E. Purdv, J. S., M.D. Pycroft, A. T. Eangihiroa, Dr. Eeid, J. Eenshaw, F. Eoberton, E., M.D. Eobertson, W. A. Eocbe, H., Waihi Eolfe, W. Seegner, C. Segar, Professor H. W. Shakespear, E. H., Little Barrier Island. Sharman, E. W., L.E.C.P. Shaw, H. Simson, T. Sinclair, A. Smeeton, H. M. Smith, H. G. S, Smith, S. Percy, F.E.G.S., New Plymouth Smith, W. H. Somerville, J. M. Speight, W. J. Spencer, W. C. C. Stewart, J., C.E. Stopford, E., iM.D. Streeter, S. C. Stringer, H. G. Thonaas, Professor A. P. W. Tibbs, J. W. Tinne, H., London Upton, J. H. Urquhart, A. T., Karaka Vaile, E. E. Walsh, Archdeacon P. Waterworth, A. Ward, P. Webster, J., Hokianga Webster, W. G. Weetman, S., F.E.G.S. Wells, T. U. Williams, Eight Eev. W. L., Bishop of Waiapu, Napier Wilson, A. P. Wilson, W. E. Withy, B., Eotorua Wyllie, A., C.E. Yates, E. Young, J. L, 460 Appendix. PHILOSOPHICAL INSTITUTE OP CANTERBURY. [* Life members."! Acland, Dr. H. D. Adams, T. W. Adamsou, Eev. H. Allison, H. Andersen, Johannes C. Aschmann, C. T., B.A. Bealey, S. Beaven, A. W. Bell, N. M., B.A. Bevau-Brown, C. E., M.A. Bernstein, Eev. I. A. Bishop, F. C. B. Bishop, E. C. Blunt, Professor T. G. E., M.A. Boag, T. D. Booth, G. T. Bowen, Hon. C. C, M.A., F.E.G.S. Brauer, H,, Ph.D. Bridges, G. G. Brooker, F. J. Brown, Professor Macmillan, M.A., LL.D.* Bruce, H. A. Buddo, D., M.P. Burley, W. E., B.A. Carlisle, W. J. Carrington, Eev. C. W., M.A. Chappell, Eev. A. B., M.A. Chilton, Prof. C, M.A., D.Sc, M.B., F. L.S.- Clark, S. A., B.A. Cockavne, L., Ph.D. Cocks," Eev. P. J., B.A. Coles, W. E. Cook. H. D.,M.Sc. Craddock, A. E., B.Sc. Crooke, Dr. L. Cross, Miss B. D., B.A. Cull, J. E. L.,B.E. Cuthhert, E., C.B. Dash, Charles Denniston, Mr. Justice Diamond, Dr. Drummond, James, F.L.S. Enghsh, E., F.C.S., M.I.M.B. Enys, J. D. * Evans, Prof. W. P., M.A., Ph.D. Farr, C. Coleridge, A.M.Inst.C.E. Farrow, F. D., B.A. Fisher, J. Bickerton Florance. D. C. H., M.A. Flower, A. E., M.A., M.Sc. Ford, C. E., F.E.G.S. Foster, T. S., M.A. Freeman, Miss, B.A. Garforth, Miss Gibson, Dr. F. G. Grant, Miss Gray, G., F.C.S. Grigg, J. C. N. Grimes, Et. Eev. Bishop, D.D. Guthrie, Dr. J. Hall, Mrs. J. Hallenstein, P. L. Hansen, B. E., M.Sc. Hardie, C. D , B.A. Hight, Dr. J., Litt.D. • Hilgendorf, F. W., M.A., D.Sc. Hill, Mrs. Carey Hitchings, F. Hodgson, T. V., F.L.S. Hogg, E. G., M.A. Howell, J. H., B.Sc. Humphreys, G. Hutton, Mrs. Inghs, Dr. H. M. Ingram, John Iredale, T. Irving, Dr. W. Jackson, T. H., B.A. Jameson, J. O. Jamieson, J. S. Jekyll, H. J. C. Kaye, A. Keir, T. Kidson, E. E., M.Sc, Kidson, G. E. Kirkaldy, G. W. Kitchingman, Miss, M.A. Kohn, E. Laing, E. M., M.A., B.Sc Laurenson, G., M.P. Lester, Dr. G. Lewin, G. A. Louisson, Hon. C. Lowrie, W. M., B.A. Macbeth, N. L. Mayne, J. B., B.A. Marshall, Mrs. McCallum, P., M.Sc. Roll of Members. 461 McKav, E. J. Hears' H. 0. D. Merton, Mrs. A. J. Meredith-Kaye, E. K. Mickle, Mrs. Mill. Dr. Thomas Mollett, T. A.- Molineaux, M. Moorhouse, Dr. B. M. Moreland, Eev. C. H., M.A. Moreland, Mrs.. M.B. Mulgan, E. K., M.A. Murray-Aynsley, H. P. Nairn, E. Olliver, W. E. B. Olliver, Miss F. M., M.A., B.Sc. Opie, C. H. A. T. Page, S., B.Sc. Pairraan, Dr. Palmer, J. Patterson, A. M., M.E.C.V.S. Poulsen, John Powell, P. H., M.Sc. Purnell, C. W. Eeeee, William Eelph, E. W. Eevell, P. Ehodes, Capt. E. Heaton, M.P. Ehodes, A. E. G. Eitchie. T., B.A. Eowe, T. W., M.A., LL.B. Scott, Henry Scott, J. L. Scott, Professor E. J., M.Inst.C.E. Seager, C. A. Sheard, Miss F., M.A. Shrimpton, E. A. Simmers, G. A. Sims, A., M.A. Skey, H. F., B.Sc. Sloman, C. J. Smith, J. Hartley, M.A. Snow, Colonel Speight, E., M.A., B.Sc, F.G.S. Spiller, J. Stead, E. F. Stevenson, Dr. J. Stone, F. Symes, Dr. W. H.- Talbot, Dr. A. G., M.A. Tavlor, A. Taylor, G. J. Terry, F. W. Thomas, Dr. W.* Thornton, S. W. Tripp, C. H., M.A.- Turner, E. PhiUips Waite, Edgar E., F.L.S. Waller, F. D., B.A. Wallich, M. G. Waymouth, F. Wavmouth, Mrs. F. Weston, G. T., LL.B. Whitaker, C. Godfrey Wigley, W. C. H., LL.B. Wilding, Frank C. Wilkins, C. W^ilkinson, Miss Williams, G. J., M.Inst.C.E. Wilson, Miss Wright, A. M., F.C.S. Wright, W. S. 462 Appendix. OTAGO INSTITUTE. [* Life members.] Alexander. Dr. Edward Allan, Dr. W., Mosgiel Allen, James, M.A., M.P. Armstrong, F. Barnett, L. E.,M.B., F.E.C.S. Batchelor, F. E., M.D., M.E.C.S. Bathgate, Alexander''' Bell, A. D., Shag Valley Benham, Professor W. B., D.Sc, F.E.S. Black, Alexander''' Black, Professor J. G., D.Sc. Blair, John Bowman, John Braithwaite, Joseph, J. P. Brent, Daniel, M.A."' Brown, William Browne, Robert Buchanan, N. L., Colli ngwood''- Burnside, J. A. Chamberlain, C. W. Chapman, C. R. Chapman, Judge F. R. Chisholm, Robert Clarke, E. S. Collier, E. E. Colquhoun, D., M.D., M.R.C.S. De Beer, I. S. Don, J. R., D.Sc. Duncan, Peter Evans, Dr. William Eels, Willi Fenwick, George Fergus, Hon. Thomas Ferguson, H. Lindo, M.D., F.R.C.S.I. Fisher, Thomas R. Fitchett, Frank, M.B. Fulton, Robert, M.D., CM. Fulton, S. W., Melbourne^*' Gilkison, Robert Gould, Ven. Archdeacon Goyen, P.,F.L.S. Graham, Thomas Sherlock Grave, W. G., Oamaru Hamilton, A., Wellington'^' Hamilton, Harold Hay, C. W. Henton, James William Herbert, E. Hocken, T. M., M.R.C.S., F.L.S. Hosking, J. H., K.C. Howes, G. W., F.E.S. James, Alfred Jeffery, James Johnstone, James Armour Kempthorne, T. W. King^ F. Truby, M.D., CM., B.Sc. Lamb, Tompson Lee, G. Livingston, W. Louden, John Lusk, T. W. McKellar, Dr. McKerrow, James, F.R.A.S. McKnight, Miss S., M.A., M.Sc. Macleod, William McPhee, J. H. Malcolm, Professor John, M.D. Marchant, Miss M. E. A., M.A. Marshall, Professor P., D.Sc, M.A. Mason, John Blair Massey, Horatio, Invercargill Matthews, H. J. Melland, E., England* Moore, Dr. Stuart, M.B. Morrell, W. J., M.A. Nevill, Most Rev. S. T., D.D. Nisbet, Rev. Dr. Ogston, Frank, M.D. Oliver, F. S. Park, Professor James Parr, E. J., M.A., B.Sc. Pavne, Francis William Petrie, Donald, M.A., F.L.S. , Auck- land"''' Pickerill, Professor Rawson, G. A. Reid, Donald, jun. Richards, Professor D. J., M.A. Richardson, Charles R. D., M.A. Riley, Frederick, M.B. Ritchie, Dr. Russell Ritchie, J. M. Roberts, John, C.M.G. Roberts, W. S., M.R.C.S. Russell, George Gray Sargood, Percy R. Scott, Professor J. H., M.D. Shacklock, John B. Shand, Professor J., M.A., LL.D. Shennan, Watson Boll of Members. 463 Sidey, John Sim, Judge William A. Sise, G. L. Skey, Henry Smitli, Joseph Crosby, Invercargill Statham, Fr. Hadfield, A.O.S.M. Stewart, William Downie Stout, Sir Eobert, K.C.M.G., Wel- lington Theomin, D. Thomson, G. M., F.L.S., M.P.- Thomson, J. C. Thomson, Eobert G. Trimble, W. H. Waters, Daniel B., A.O.S.M. White, David E., M.A. Whitson, T. W\ Williams, Dr. Ernest Williams, H. Bradlev. Williams, Judge, M.A., LL.M. Woodhouse, J. F. Young, Dr. James, Invercargill WESTLAND INSTITUTE. (No list sent in.) HAWKE'S BAY PHILOSOPHICAL INSTITUTE. [* Life members.] Andrews, E. W. Antill, H. W., Kumeroa Asher, Eev. J. A. Bernau, Dr. H. F. Burnett, H., Woodville Chambers, J. B., Te Mata Chambers, J., Mokopeka Chambers, W. K., Waerengaahika, Poverty Bay Clark, Gilbert Clark, Thomas, Eskdale Clarkson, E. P., M.A. Coe, J. W. Cooper, S. E. Craig, J. W. Crawshaw, George Darton, G., Gisborne De Lisle, Dr., Hastings Dinwiddie, P. Dinwiddle, W. Donnelly, G. P., Crissoge Duncan, Eussell Edgar, Dr. J. J. Guthrie-Smith, H., Tutira Hall, T. Hamilton, A., Wellington''' Harding, J. W., Mount Yernon Henlev, Dr. E. A. W. Hill, H., B.A., F.G.S. Hislop, J.* Holder, H. E., Woodville Holdsworth, J., Havelock N. Hutchinson, F., jun., Eissington Hyde, Thomas Kennedy, Dr., Meeanee Kerr, W. 'Kinder, J., M.A., Gisborne Large, J. S.* Large, Miss Lawry, Eev. A. C. Leahy, Dr. J. P. Locking, Dr. B. Lowry, T. H., Okawa Luff, A., Wellington McLean, E. D. D. Mavne, Eev. Canon Moore, Dr. T. C. Olsen, H., Norsewood S. Ormond, G., Mahia Ormond, Hon. J. D., M.L.C. O'Eyan, W., Waipiro Eowley, F., B.A., Gisborne Sinclair, G. H., Clive Sherwood, T. E., Makarika, Wai- piro Bay Sheath, J. H. Smith, J. A., B.A. Smith, J. H., Olrig* Spencer, Miss Tanner, T. Tiffen, G. W., Wheturau, Gisborne Townley, J., Gisborne White, T., Wimbledon Wilhams, F. W. Williams, G. T., Matahiia, Tuparoa, East Coast Williams, J. N., Frimley, Hastings Williams, Eev. H., Gisborne Willis, H., Hopelands 464 Appendix. NELSON PHILOSOPHICAL INSTITUTE. (No list sent in.) MANAWATU PHILOSOPHICAL SOCIETY. Abraham, R. S. Armstrong, E. J., C.E. Bagnall, J. J. Baldwin, P. E. Barnicoat, J. L. Barraud, E. N. Batchelor, F. S. Bendall, W. E. Bond, F. W. Charlesworth, Cohen, M. Cooke, F. H. Davis, R. Drake, A. Durward, W. F. EHott, M. A. Fitzherbert, W. L. Foote, F., B.Sc. Frankland, F. W. Gardner, R. Gerrand, J. B. Glendinning, A. A. Goldingham, F. S. Graham, A. J. Greig, Dr. Guy, A. Hankins, J. H. Harman, V. Harper, Rev. C. C, M.A. Hewitt, Captain, R.N. Hoben, E. D. Hodder, T. R. Jackson, F. L. Jickell, S. Johnston, J. M. Jolly, Rev. I. Keehng, R. N. Kerslake, H. Low, D. W. McKenzie. D. H. Manson, Thomas Martin, Dr. A. A. Martin, Donald Mellsopp, Mrs., M.A. Mitchell, J. Monckton, C. A. W. Mowlem, H. -Nash, J. A. O'Donnell, W. J. Park, W. Payne, W. H. Peach, Dr. Preece, Captain Putnam, Dr. Richardson, T. F. Russell, A. E. Scott, J. G. Seifert, A.. Seifert, L. Sinclair, D. Smith, W. W. Stephenson, Rev. G. B. Stevens. John Stowe, Dr. W. R. Strang, W. Tatton, Dr. A. Vernon, J. E., M.A. Waldegrave, C. E. Warburton, E. Warden, C. H. Watson, F. E. Welch, W.. F.R.G.S. Williams, G. Wilson, Dr. G. Wilson, K., M.A. Wollerman, H. List of Free Copies. 465 LIST OF INSTITUTIONS TO WHICH THIS VOLUME IS PRESENTED BY THE GOVERNORS OF THE NEW ZEALAND INSTITUTE. Honorary Members of the New Zealand Institute, 30. Neto Zealand. Cabinet, The Members of, Welhngton. Executive Library, Wellington. Free Public Library, Auckland. „ Christchurch. „ Dunedin. „ Wellington. Government Printer and publishing staff (6 copies). Library, Auckland Institute, Auckland. Auckland Museum, Auckland. Biological Laboratory, Canterbury College, Christchurch. Biological Laboratory, University College, Auckland. Biological Laboratory, University of Otago, Dunedin. Biological Laboratory, Victoria College, Wellington. Canterbury Museum, Christchurch. Dunedin Athengeum. General Assembly, Wellington. Hawke's Bay Philosophical Institute, Napier. Manawatu Philosophical Society, Palmerston North. Nelson Institute, Nelson. New Zealand Institute of Surveyors. New Zealand Institute, Wellington. Otago Institute, Dunedin. Otago Museum, Dunedin. Otago School of Mines, Dunedin. Philosophical Institute of Canterbury, Christchurch. Polynesian Society, New Plymouth. Portobello Fish-hatchery, Dunedin. Reefton School of Mines. Thames School of Mines. University College, Auckland. University College, Christchurch. University of Otago, Dunedin. Victoria College, W^ellington. Wanganui Museum. Wellington Philosophical Society. Westland Institute, Hokitika. Great Britain. Anthropological Institute of Great Britain and Ireland, London. British Association for the Advancement of Science, Loudon. British Museum Library, London. „ Natural History Department, South Kensington, London, S.W, 16— Trans. 466 Appendix. Colonial Office, London. Clifton College, Bristol, England. Entomological Society, London. Geological Magazine, London. Geological Society, Edinburgh. „ London. Geological Survey of the United Kingdom, London. High Commissioner for New Zealand, London. Imperial Institute, London. Institution of Civil Engineers, London. International Catalogue of Scientific Literature, London. Kegan, Paul, Trench, Triibner, and Co., London (x^gents). Leeds Geological Association, Meanwood, Leeds. Linnsean Society, London. Literary and Philosophical Society, Liverpool. Liverpool Biological Society. Marine Biological x\ssociation of the United Kingdom, Plymouth. Natural History Society, Glasgow. Marlborough College, England. Nature, The Editor of, Loiidon. Norfolk and Norwich Naturalist Society, Norwich. North of England Institute of Mining and Mechanical Engineers, Newcastle-upon-Tyne. Patent Office Library, London. Philosophical Society of Glasgow. Philosophical Society of Leeds, England. Eoyal Asiatic Society, London. Eoyal Botanic Garden Library, Edinburgh. Royal College of Physicians, Edinburgh. Royal Colonial Institute, London. • Royal Geographical Society, London. Royal Irish Academy, Dublin. Royal Physical Society, Edinburgh. Royal Society, Dublin. „ Edinburgh. „ London. Royal Society of Literature of the United Kingdom, London. Royal Statistical Society, London. School Librtiry Committee, Eton, England. „ Rugby, England, University Library, Cambridge, England. „ Edinburgh. „ Oxford, England. Victoria College, Manchester. Victoria Institute, London. Zoological Record, London. Zoological Society, London. British North America. Canadian Institute, Toronto. Geological and Natural History Survey of Canada, Ottawa. Hamilton Scientific Association, Hamilton, Canada. Institute of Jamaica, Kingston. Literary and Historical Society of Quebec, Canada East. Natural History Society of New Brunswick, St. John's. List of Free Copies. 467 Nova-Scotian Institute of Natural Science. Halifax. Ottawa Literary .and Scientific Society, Ottawa. South Africa. Free Public Library, Cape Town. South African Philosophical Society, Cape Town. South African Association for the Advancement of Science, Cape Town. South African Museum, Cape Town. Rhodesia Museum, Bulawayo, South Africa. Bidia. Asiatic Society of Bengal, Calcutta. Colombo Museum, Ceylon. Geological Survey of India, Calcutta. Natural History Society, Bombay. Raffles Museum, Singapore. Queensland. Geological Society of Australasia, Queensland Branch, Brisbane. Geological Survey Office, Brisbane. Library, Botanic Gardens, Brisbane. Queensland Museum, Brisbane. Royal Society of Queensland, Brisbane. Neio South Wales. Agricultural Department, Sydney. Australasian Association for the x\dvancement of Science, Sydney Australian Museum Library, Sydney. Department of Mines, Sydney. Engineering Association of New South Wales, Sydney. Library, Botanic Gardens, Sydney. Lmnsean Society of New South Wales, Sydney. Public Library, Sydney. Royal Geographical Society of Australasia, N.S W. Brancb, Sydney. Royal Society of New South Wales, Sydney. University Library, Sydney. Victoria. Australian Institute of Mining Engineers, Melbourne. Field Naturalists' Club, Melbourne. Geological Survey of Victoria, Melbourne. Gordon Technical College, Geelong. Legislative Library, Melbourne. Public Library, Melbourne. Royal Society of Victoria, Melbourne. University Library, Melbourne. Victorian Institute of Surveyors. Tasmania. Public Library of Tasmania, Hobart. Royal Society of Tasmania, Hobart. South Australia. Royal Society of South Australia, Adelaide. University Library, Adelaide. 468 Appendix. Russia. Finskoie Uchonoie Obshchestvo, Finnish Scientific Society, Helsing- fors. Imper. Moskofskoie Obshchestvo lestestvo - Ispytatelei, Imperial Moscow Society of NaturaUsts. Kiefskoie Obshchestvo lestestvo-Ispytatelei, Kief Society of Natural- ists. Nonvay. Bergens Museum, Bergen. University of Christiania. Siveden. Geological Survey of Sweden, Stockholm. Koyal Academy of Science, Stockholm. Denviark. Natural History Society of Copenhagen. Royal Danish Academy of Sciences and Literature of Copenhagen. Germany. Botanischer Verein der Provinz Brandenburg, Berlin. Konigliche Bibliothek, Berlin. Konigliche Physikalisch-Oekonomische Gesellschaft, Konigsberg, E. Prussia. Konigliches Zoologisches und Anthropologisch - Ethnographisches Museum, Dresden. Naturhistorischer Yereiu, Bonn. Naturhistorisches Museum, Hamburg. Naturwissenschaftlicher Verein, Bremen. Naturwissenschaftlicher Verein, Frankfort-an-der-Oder. Rautenstrauch-Joest-Museum (Stiidtisches Museum fiir Volkerkunde), Cologne. Redaktion des Biologischen Central-Blatts, Erlangen. Senckenbergiscbe Naturforschende Gesellschaft, Frankfurt-am-Main. Verein fiir Vaterlandisehe Naturkunde in Wiirttemburg, Stuttgart. Austria. K.K. Central- Anstalt fiir Meteorologie und Brdmagnetismus, Vienna. K.K. Geologische Reichsanstalt, Vienna. Belgiwn a7id the Netherlands. Musee Teyler, Haarlem. Academie Royal des Sciences, des Lettres, et des Beaux- Arts de Belgique, Brussels. La Societe Royale de Botanique de Belgique, Brussels. Sivitzerland. Musee d'Histoire Naturelle de Geneve. Naturforschende Gesellschaft (Societe des Sciences Naturelles), Bern. France. Bibliotlieque Nationale, Paris. Musee d'Histoire Naturelle de Bordeaux. Musee d'Histoire Naturelle, Paris. Societe Entomologique de France, Paris. Societe de Geographic, Paris. Societe Zoologique de France, Paris. List of Free Copies. 469 Italy. Biblioteea ed Archivio Tecnico, Kome. Museo di Geologia e Paleontologia del E. Instituto di Studi Superiori, Florence. Mvxseo di Zoologia e di Anatoniia Comparata della R. Universita, Turin. Orto 6 Museo Botanico (R. Instituto di Studi Superiori), Florence. R. Accademia di Scienze, Lettre, ed Arti, Modena. R. Accademia dei Lincei, Rome. Stazione Zoologica di Napoli, Naples. Societfi Africana d'ltalia, Naples. Societa Geografica Italiana, Rome. Societa Toscana di Scienze Naturali, Pisa. Utiited States of America. xAcademy of Natural Sciences, Buffalo, State of New York. „ Davenport, Iowa. „ Library, Philadelphia. „ San Francisco. American Geographical Society, New York. American Institute of Mining Engineers, Philadelphia. American Museum of Natural History, New York. American Philosophical Society, Philadelphia. Boston Society of Natural History. Connecticut Academy, New Haven. Department of Agriculture, Washington, D.C. Field Museum of Natural History, Chicago. Franklin Institute, Philadelphia. Johns Hopkins University, Baltimore. Missouri Botanical Gardens, St. Louis, Mo. Museum of Comparative Zoology, Cambridge, Mass. Natural History Museum, Central Park, New York. New York Academy of Sciences. Philippine Museum, Manila. Rochester Academy of Sciences. Smithsonian Institution, Washington, D.C. Stanford University, Cahfornia. Tufts College, Massachusetts. United States Geological Survey, Washington, D.C. University of Montana, Missoula. Wagner Free Institute *of Science of Philadelphia. Washington Academy of Sciences. Brazil. Museu Paulista, Sao Paulo. Escola de Minas, Rio de Janeiro. Argentine Republic. Sociedad Cientifica Argentina, Buenos Ayres. Uruguay. Museo Nacional, Monte Video. 470 Appendix. Japan. College of Literature, Imperial University of Japan, Tokyo. College of Science, Imperial University of Japan, Tokyo. Hawaii. Bernice Pauahi Bishop Museum, Honolulu. National Library, Honolulu. Java. Society of Natural Science, Batavia. INDEX. AUTHORS OF PAPERS. Page Adams. C. E. " The Wellington Tide-gauge " .. .. .. ..406 Andersen. Johannes C. " Natural Classification of English Poetry ". . .. 410 " Australian Modification of the English Ballad " . . 418 " New Zealand Bird-song " .. .. 422 Best, Elsdon. " Maori Forest Lore : Part II " .. ..231 Broun, T. " Coleoptera from the Chatham Islands " . . . . . . 145 " New Zealand Co.s.so?u(Zffi " .. .. .. .. .. 151 Cheeseman, T. F. " Description of a Species of Bztrmajmittcetc" .. .. 140 Chilton, C. "Yre3h--watev Amphipoda" .. .. .. .. ..53 " Notes on Amphipodan Genera " .. .. .. ..59 Cockayne, L. " New Plant-habitats (IV) " . . . . . . . . . . 399 " Plants from the Solanders " .. .. .. .. 404 " Aerial Rhizomes of Cord?/ Zfne " .. .. .. .. 405 Cotton, C. A. " Geology of Signal Hill, Dunedin " .. .. .. ..Ill Donovan, W., and J. S. Maclaurin. " Estimation of Iron in Iron-ores " . . 49 Drummond, J. " Birds on Kapiti Island ". . .. .. .. ..30 Farquhar, H. " New Zealand Starfishes " .. .. .. .. .. 126 Finlayson, A. M. " Quartz Veins of Otago " . . . . . . . . 64 " Reef ton Gold-veins " . . . . . . . . . . 85 Fitchebt, F. " Physiological Action of Tutin " .. ' .. .. ..286 Gudex, M. C. " Striated Stones from the Waimakariri " . . . . . . 33 Hamilton, A. '• Le^'i'^o^Jfera from Lake Wakatipu ". . .. .. ..44 Hill, H. " The Great Wairarapa " .. .. .. ..429 •' Dactyla7ithus Tmjloi-i'^ .. .. .. .. .. .. 437 Hogg, Evelyn G. " On the Harmonic Conic of Two Given Conies " . . . . 34 " On certain Conic-loci of Isogonal Conjugates " . . . . 38 Kirkaldy, G. W. " ifenii^^iera of the Maorian Subregion " .. .. ..22 Maclaurin, J. S., and W. Donovan. " Estimation of Iron in Iron-ores" . . 49 Marshall, P. " Geology of Rarotonga and Aitutaki " .. .. ..98 " Contact Rocks from West Nelson " .. .. .. .. 101 " Crater of Ngauruhoe " .. .. .. .. ..102 „ " New Zealand Minerals " .. .. .. .. .. 105 " New Zealand Fossil Ce^'/iaioporfa " .. .. .. 143 Meyrick, E. " New Zealand LepirfojJfera .. .. .. .. .. 5 Newman, A. K. " A Rare Maori Implement " .. .. .. .. 216 Petrie, D. " New Species of Epilohium " . . . . . . . . . . 140 Segar, H. W. " The Trisection of an Angle " .. .. .. ..218 "Insanity: Comparative Statistics " .. .. .. .. 221 Skey, H. " On the Decimal Currency " .. .. .. .. ..16 Smith, S. Percy. " D'Urville's Visit to Tologa Bay " .. .. ..130 Smith, W. W. " Nesting Habits of /J/a^irf//r« /?(t6eIZi/era " .. .. .. 1 Speight, R. " Hornblende-andesite from the Solander Islands" . . . . 52 Stuckey, F. G. A. "New Zealand Actinian, Biinodes aureoradiata" .. .. 367 " Two Anemones from near Wellington " . . . . 370 " New Zealand Actiniaria " .. .. .. .. 374 Wright, A. M. " Analysis of Sliped Wool " . . . , . . . . 42 John Mackay, Government Printee, Wellington. — 1909. V"^ TEANSACTIONS OT THE NEW ZEALAND INSTITUTE 1908 VOL. XL! (Kbw Isbcb) EDITED AND PUBLISHED UNDER THE 'AUTHORITY OF THE BOARD OF GOVERNORS OF THE INSTITUTE Issued June, 1909 WELLINGTON, N.Z. JOHN MACKAY. GOVEBNMENT PRINTING OFFICE KBOAN, PAUL, TBEMCH, TBCBNEB, AND CO., FATEBNOSTEB HOUSE CHABINO OBOSS BOAD, LONDON MBL WHOl LIBRARY lilH n(3(3 P mil m m