Pee ae oe aise. co. ae 4 ahgtt THE ery SOCTETY. MDCCCXLIV. INSTITUTED This volume is issued to the Subscribers to the RAY Society for the Year 1876. LONDON: MDCCCLXXVIII. ag ae % obey, % OF THE FREE AND SEMI-PARASITIC Wie COPEPODA OF THE BRITISH ISLANDS. BY So LNWARDSON BRADY, M.D., F.L:S8.; PROFESSOR OF NATURAL HISTORY IN THE UNIVERSITY OF DURHAM COLLEGE OF PHYSICAL SCIENCE, NEWCASTLE-ON-TYNE; CORRESPONDING MEMBER OF THE ZOOLOGICAL SOCIETY OF LONDON, OF THE ACADEMY OF NATURAL SCIENCES OF PHILADELPHIA, ETC. WOE; 1: COLLACTION PRINTED FOR THE RAY SOCIETY. LONDON: MDCCCLXXYVIIi. 137% Pe 4 ‘= Seu ht ignors®.. ia nee Oe nae Serna, coe roan — Woe rs a ACL ou.. ee . A MONOGRAPH OF THE BRITISH FREE AND SEMI-PARASITIC COPEPODA. INTRODUCTION. Since the publication, by the Ray Society in 1850, of Dr. Baird’s work on the ‘ British Entomostraca,’ much has been done by various authors m this country as well as on the Continent of Hurope and in America, to extend our knowledge not only of the morphology and physiology of the group, but also of its distribu- tion, both fossil and recent. Dr. Baird’s work admi- rably fulfilled its purpose of gathering together what was at that time known of the British species, a very large amount of this knowledge being derived from the painstaking researches of the author himself. And though now of necessity somewhat obsolete owing to the continued labours of more recent col- lectors, no one who has studied the ‘ British Entomos- traca’ can fail to have been largely indebted to Dr. 2, BRITISH COPEPODA. Baird’s work, which must always take rank among the classics of natural history. The number of species of non-parasitic Copepoda noticed by Dr. Baird is thirteen, since which time several species, both fresh-water and marine, have been described by Sir John Lubbock, the Rev. Alfred Merle Norman, the late H. Goodsir, and by myself both singly and in conjunction with my friend, Mr. David Robertson, of Glasgow. The species com- prised in this Monograph will number, so far as at present appears, one hundred and fifty-one. The truly parasitic forms—fish-lice, &c., are ex- cluded as not coming within the scope of my work. They are of themselves sufficient to occupy an independent volume, and to afford abundant work to any naturalist whose time and opportunities allow of his taking them in hand. The researches of recent German writers—espe- cially of Dr. Claus—on the physiology, minute anatomy, and embryology of the Entomostraca, are so full and exhaustive, that anything I could have said on those subjects would have been a mere epitome of what can be better studied in the works of those authors. J have, therefore, in the following pages, confined my descriptions to the external form, not travelling into details of physiological anatomy except so far as necessary for purposes of classification and specific description.* I have not thought it needful to give exhaustive * Thope, however, in an introduction to the second volume, to give a brief outline of the state of our knowledge on these subjects. INTRODUCTION. 3 lists of specific synonyms, this, in the case of species known to the older authors having been excellently done by Dr. Baird. I have, however, given as fully as possible references to the descriptions of more recent observers, and when practically useful, also to those of older date, omitting such only as seemed to be of slight or merely literary interest. A list of the memoirs from which these details are taken is printed at p. 27. The great majority of the Copepoda are free swim- ming species, a considerable number, however, being truly parasitic and living suctorially on the juices of Fishes, Annelids, Crustacea, and other aquatic animals. These do not enter into the scope of the present work. Another group, which may be called semi-parasitic, is found living (not suctorially nor attached in any way to the body of the host, but moving freely) in the cavities of various marine animals, notably in those of Ascidians, both simple and compound. The genera Notodelphys, Botachus, Ascidicola, Doropygus, Licho- molgus, and Notopterophorus are among the most important of this group. M. Hesse, of Brest, has closely studied these animals, and has described many species; as also have MM. Claparéde, T. Thorell, Van Beneden, and others. Some species have also been found, perhaps living suctorially—though this is open to doubt—on the outer surfaces of sponges, sea- urchins, and star-fishes; to this list belong some members of the genus Artotrogus. These semi- parasitic Copepoda exhibit for the most part a transitional condition of the mouth organs, inter- A, BRITISH COPEPODA. mediate between the true biting and chewing apparatus of the free swimming species, and the true suctorial mouth of the fish-lice and other thorough-going parasites. From a consideration of these peculiarities M. Thorell has proposed to arrange the Copepoda under three sections—Gnathostoma, Pecilostoma, and Siphonostoma—which arrangement though adopted by Claparéde and others is rejected by Claus chiefly, as it appears, owing to a difference of opinion as to the homologies of the various mouth organs. In this work I adopt the three divisions proposed by M. Thorell, because whatever opinion may be held as to the nature of the component parts of the mouth apparatus, each division seems to repre- sent a well-marked natural group. Some remarks on this part of the subject will be found at greater length under the definition of the group Pecilostoma. Throughout the whole class Crustacea the mouth organs, and other cephalic appendages, are liable to the most profound modification according to the needs and circumstances of particular groups, and on this account the conformation of these parts offers a most natural and trustworthy guide to classification. In no order is this more conspicuously the case than in the Copepoda, which, from the lowest and absolutely inactive Epizoa,* to the most agile and highly organised of the free swimming Calanide, offer an endless variety of structure. So rudimentary, indeed, in development, are some of the lower EKpizoa, * These, however, are often separated from the Copepoda to form an independent order. INTRODUCTION. D that without the evidence derived from the study of their embryology, and the successive phases of their life history, it would be impossible to assign them with any certainty to the place which they are now held rightly to occupy in the scheme of nature. And though none of the species which form the subject of the present Monograph, differ so widely as this, one from another, there yet exist variations of great interest pointing to very decided differences in mode of life. Next to the mouth organs, the anterior antenne and the first and last pairs of swimming feet exhibit the most important variations of structure, the distinctive peculiarities of these parts being mostly connected with the sexual function, and therefore most fully developed in the male sex. The anterior antenna, which in the female is usually a simply-jointed, slender, tapering limb, in the male not unfrequently becomes partially swollen, nodose, hinged, or provided with serrated plates for the purpose of affording a more efficient grasp of the female, these modifications occurring sometimes in one antenna only, as in many Calanidze, sometimes in both, as in Cyclopide. The modifications of the fifth pair of feet are very various ; in some of the Calanide they become very powerful auxiliary clasping organs, but more generally they are quite rudimentary in both sexes (Cyclopide), while in most Harpacticide, though rudimentary in the male, they are usually somewhat more largely developed in the female, where they are foliaceous in character and appear to act as a support or protection to the external ovisac. 6 BRITISH COPEPODA. The colouring of the Copepoda varies very con- siderably, as does that of many larger Crustacea, with that of their food material and of the vegetation amongst which they lve; a large number of the oceanic species are translucent and almost colourless, but one of these — Anomalocera Paterson — often exhibits wonderfully brilliant tints of blue, red, and green; Peltidiwm interruptum, which is also chiefly an oceanic species, 1s constantly of a deep reddish-brown colour, and almost all the flat-bodied species (Pel- tididz, Claus) are banded to some extent, sometimes very gorgeously, with shades of red or purple; the same may be said of some few species of Harpacticide, notably of Yhalestris rufocincta, Norman, 1’. longi- mana, Claus, 7’. rufoviolascens, Claus, and Westwoodia nobilis, Baird. The colours of most of these are given as faithfully as possible in the plates illustrating the various species. ‘The usual colour of the marine Copepoda, however, is a transparent yellowish brown or straw colour, against which the eye shows as a spot of brilliant ruby red, the internal digestive and glandular organs often being apparent as patches of a darker brown. ‘The ovisacs, especially in some fresh water species, not unfrequently exhibit characteristic tints of blue, brown, or green; but the colouring of the inhabitants of fresh water seems to vary remark- ably according to the locality and nature of food. Thus, Diaptomus Castor, Jurine, is usually of some shade of light brown, often with bluish ovisacs; but in an elevated Westmorland tarn I have found it of a brilliant vermilion red; and in peaty pools of no very INTRODUCTION. 7 great elevation I have noticed Cyclops serrulatus to assume adeep brownish-red colour. Similar instances of variation might be noted in respect of many other species. It is, nevertheless, very remarkable that in many gatherings of Copepoda, the various species (or at least some of them) may be unerringly picked out by attending to the characters of colour only, and, indeed, this is practically often by far the readiest way of separating species under the low magnifying power of a hand-lens. Amongst the non-parasitic Copepoda there is very great diversity of habit. Many of the marine species pass their life apparently near the surface of the open sea, and some of these—such as Calanus finmarchicus, Gunner, and Anomalocera Paterson, Templeton, are frequently found in immense profusion, the first- named species having been said to form a very important part of the food of the Greenland whale, and it is remarkable that in the Arctic Seas not only do the Entomostraca attain an enormous development in point of members, but also in individual size; Arctic specimens, for example, of Calanus finmarchicus and Metridia armata being many times the bulk of those taken in our own latitude; the same observation is well known to hold good in respect of the higher Crustacea, Amphipods, &c., as has been pointed out to me by the Rev. A. M. Norman. A large number of species haunt almost exclusively the forests of Laminariz which grow on rocky coasts, at and below low-water mark; the fronds of Laminaria saccharina in particular are the favourite abode of many species, 8 BRITISH COPEPODA. more especially of the flat-bodied Porcellidiine and their allies, which appear to find shelter in the numerous inequalities of its rugose fronds. Amongst the groves of smaller algee with which tidal rock-pools are often so densely overgrown, Copepoda are always to be found in abundance, but though I have paid particular attention to the matter I have not found that the different species have any particular prefer- ences as to the kinds of weeds which they haunt ; it is probable that shelter rather than food is the reason of their liking for these marine forests. The brackish water of salt marshes and small estuaries sustains a peculiar Entomostracan fauna, the most characteristic members of which, amongst the Copepoda, are Temora velox, Lilljeborg, TLachidius brevicorms, Miller, and, less commonly, Cyclops isignis, Claus, Nannopus palustris, Brady, Platychelipus littoralis, Brady, Meso- chra Lilljeborgii, Boeck, and Delavalia palustris, Brady; with these there is usually associated a peculiar group of Ostracoda, Cythere castanea, Sars, Cytheridea torosa, Jones, Loxoconcha elliptica, Brady. The Mala- costraca, Foraminifera, and other branches of the fauna of such localities present likewise features of ereat interest, but it is impossible here to enter fully into the consideration of the subject; the reader who desires further information is referred to the papers mentioned below.* Pools of sea water above, or at * “On the Crustacean Fauna of the Salt Marshes of Northumberland and Durham,” by G. S. Brady, C.M.Z.S. (‘Natural History Trans- actions of Northumberland and Durham,’ vol. iii). ‘“ On the Ostracoda and Foraminifera of Tidal Rivers,’ by G. S. Brady, C.M.Z5., David Robertson, F.G.S., and H. B. Brady, F.L.S. (‘Annals and Magazine of Natural History,’ ser. 4, vol vi, 1870). ‘On the Zoology of INTRODUCTION. 9 the extreme limit of high water mark, are very frequently tenanted by a single species, Harpacticus Julvus, Fischer, which is very rarely to be met with in more purely marine situations. The bed of the sea, down to the extreme depths attainable round the British Islands, is inhabited by numerous Copepoda ; on sandy bottoms the most abundant species are Longipedia coronata, Claus, and Hetinosoma spinipes, Brady, but Copepoda of some kind are found in greater or less abundance on all sorts of bottoms. One exception must be made to this statement; in various hauls from a bottom of slimy argillaceous mud, the product of the débris of disintegrating felspar rocks, taken from a depression of the depth of fifteen to twenty-five fathoms at the north end of Mulroy Lough, County Donegal, Mr. Robertson and myself could not detect one trace of life of any kind. The beds of fresh water lakes seem to be very sparsely populated with Copepoda, and as to swimming species it may, as a general rule be said that the weedier the pool and. the smaller its extent, the more abundant in all probability, the Hntomostraca. A few words as to the best modes of collecting Copepoda will not be out of place here. In the case of tidal marine pools and small fresh water ponds, such as may easily be fished from the edge, a common ring net fitted with a muslin bag and attached to the end of a walking stick will answer every purpose. This may be worked to and fro amongst the weeds Hylton Dene,” by George S. Brady (‘ Transactions of the Tyneside Naturalists Field Club,’ vol. vi). 10 BRITISH COPEPODA. or in the clear water, and the results, when cleared — from coarse débris and extraneous materials, may either be put at once into spirit or, if it is wished to keep the Entomostraca alive, into water, fresh or salt as the case may be. Marine surface-swimmers may be taken in a similar way by working the net from the side of a boat, or a tow net may be thrown over and attached to the boat by a cord. A tow net put over- board from a vessel anchored for the night in a tide- way will often be found in the morning to have made good captures. And it may be noted that surface net gatherings made during the hours of dusk or darkness are commonly of much greater interest than those taken in daytime; it seems certain that many marine Crustacea which are found near the surface at night recede towards the bottom on the approach of day- licht. Some of the pleasantest and most profitable hours which I have ever spent have been when, after a day’s dredging, I have set out at sunset on a quiet boating excursion for the purpose of capturing such prey as could be got in the surface net. Many hours of this kind spentin the company of my old friend Mr. David Robertson, amongst the Scilly Islands, on the Firth of Clyde, on the sheltered bays of Round-’ stone and Westport, or on the stormier coasts of Northumbria will long live in my memory, not only by their results in the acquisition of valuable speci- mens, but as times of unalloyed delight in the contemplation of nature under a different guise from that in which we usually see her. The washing of fronds and roots of Laminarie, INTRODUCTION. Ly which may be dragged up by means of the hooked grapnels used on many coasts by kelp burners, often affords multitudes of Copepoda. The weeds should be washed by agitation in a large tub of sea water, and when the operation is completed, the water, after being allowed sufficient time—a few seconds only— for the subsidence of coarse material, is to be poured off through a muslin net, on which the Copepoda, and probably numerous other swimming animalcula, will be intercepted. These may be cleaned while in the net by repeated douches of sea water. The products of the dredge, sand, mud, gravel, shells, &c., should be treated in a similar manner before being thrown overboard. I have no doubt that this method of procedure offers by far the best chance of extended acquaintance with the microscope life of the sea bed, and that numberless new species and interesting forms of life may be discovered by its means. The preservation of specimens is probably best effected by alcohol in the form of rectified or methy- lated spirit, but this agent has the disadvantages of destroying many colours, and of rendering the animals opaque by coagulating their albuminous tissues. Still, among the numerous solutions which have from time to time been recommended none are on the whole so convenient or efficient. Perhaps the next best is a solution of chloral hydrate (twelve grains to a fluid ounce) in camphor water. As microscopic prepara- tions, Copepoda are best mounted in some gelatinous medium containing a very small quantity of glycerine. Treated in this way mountings will keep in perfect 12 BRITISH COPEPODA. condition for many years—eternally for anything I know to the contrary—without the trouble of cement- ing round the edges of the glass cover. The formula which I habitually use is given below.* Before dissecting Copepoda for microscopic examination they should be macerated for a few hours in a solution of caustic potash ; the fatty and granular tissues are by this means removed and the details of structure rendered clearly visible; the dissection is easily per- formed under the microscope with fine needles, either with or without the help of an erector. The nomenclature of the body segments and append- ages of the Copepoda, as of the Crustacea in general, has been somewhat confused by the variety of terms applied to the same part by different authors. It is, therefore, necessary to explain the application of the terms which I have here adopted. This will be understood by an examination of the table, at p. 14, which shows the names used by some recent writers on the Entomostraca for the appendages of the first * Take any quantity of Nelson’s gelatine, and let it soak for two or three hours in cold water which has previously been saturated with arsenious acid; pour off the superfluous water, and heat the soaked gelatine until melted. To each fluid ounce of the gelatine add one drachm of alcohol and mix well; then add a fluid-drachm of the white of an egg; mix well while the gelatine is fluid, but cool. Now boil until the albumen coagulates and the gelatine is quite clear. Filter through fine flannel, and to each fluid ounce of the clarified gelatine add six fluid drachms of Price’s pure glycerine, and mix well. (‘ Carpenter’s Microscope and its Revelations,’ 3rd edition, p. 775.) It is worth notice that this preparation is injurious to calcareous structures, such, for instance, as the spicules of Echinodermata, these being in a comparatively short time completely dissolved by the glycerine. If used for preparations of this kind the glycerine should be omitted. ss CU INTRODUCTION. 13 twelve (cephalothoracic) somites. The abdominal segments in the Copepoda have no limb-like append- ages. The preparation of this Monograph has involved labour extending over several years, and in now bring- ing that labour to a close I must express my warmest thanks to all who have lent me their aid during the progress of my work. Hspecially are my acknow- ledgments due to Mr. David Robertson to whom for kind and ever active help during many pleasant excursions, as well as for gifts of numerous valuable gatherings of Copepoda, I am very largely indebted ; to the Rey. Alfred Merle Norman who with unvarying kindness and liberality has placed his valuable collec- tions at my disposal, to Mr. HE. C. Davison, R.N., of Sunderland, for many very interesting collections made during the voyages of the *‘ Porcupine”’ and at other times; to Sir John Lubbock, Dr. Claus, and M. T. Thorell for their liberal communication of information and specimens. ) Se , ‘sofa Surjsoddns oqiuos ormyeyyqdg. +4 ‘91Qv} SULOSOLOJ OY UL MATS sv spodi[[Ixvul pur we[[IxvU pUOdES pUv ysAy FO pvoysul spodi[ixvur parqy pur ‘puodes ‘4SAf SUI OY} SOSN SOUTJOULOS OS]B Yooqqnry UYOL Ag ‘smvl-qooy pur e2uuejue oy} UL Sv ‘ATWO STITT OA\4 JO SOLIOS B 04 Ade Lay} oxy A Suite 1094eq oY} 01Waysod pur worajuy yuryy JT Jfoshur 10g *.102.1ags0d ‘sowafur ‘puocoas pur ‘ 1or1vazwp ‘sovwadns ‘ys.uf spiom oy A[qvosuvyo10yur sosn oy { poyeys OA0y Sv ATQVLIVAUL Jou o.1¥ suVD “Iq Aq posn SUI0} OY, x | . “ti “49g as “ P ‘ dP pe eel “ prg [hore Plg cs puz “ce puz ce pug a ‘qooz Jo ated 48[|\"yooz Jo zed 4sT|\‘qooy Jo ared 487. o “« LOTIOJSOG « pug) ‘spodiiprxryy = ‘savel S -jooy «sotmeyuy| ‘savfl-JOo; 4ST ce . puzi 5 a0 AEM SE a al! ep eat atPRe iy SE ee fl eee OT — Sl ‘eUme} ‘euUeqUe TOL m9 “ue = LOLIOJSO « puzj-ojsod 10 puz "Vuuo} ‘BUMOUe ‘Ue JOLOJUY) “VUUOJUY YST|LOLLoJUv 10 4ST) ‘gL81_ —898T. “FOBT ‘9981 ‘Kpulg 4 “sne{9 ‘yoo0g 4, ooqqny ~—t a 73 qW9¢ “ 799) ee “ Wy) eile Se oe ‘ pug PArg ‘qooy jo ared 4sT * pre és ge jo ated 487. Z ey ‘spodiyixeyy, ‘S][IXvUl 38T| ‘S| [TXeVPy STP OA “Solqtpuey| | ‘euUUd4 « puzg-ue wed pug | eeuuey | ‘eUMOJUR 4ST|-ue aATed = 48T| “Segt ‘B1oqgolvyT eh . 6S8T GOST ‘Sieg : ‘6SBT ‘T2101, pared -maeid ome. Tie “ wpadeup “ |x « pighidowe “ xX * “pugidemn XT “Id ‘qooy Jo ued 4ST AoT VT op Soyeg] TITA . pichadoures =" TLA TA ihe « pug) id omz Id 107 Vl Op Sot ‘SsMvl-JOO} JST /-toyorut sow) A “ue LO -ue ‘so[qipuryy ‘sopnqipuryy| AT "eUUOY IOTALOFUL “ad ejnuneyUy\omzZ VT op 4uy| TIT “UO y “ad IOWOdNG oT VT op “4uy! IT — -~ re “VUOU30S “BIST ‘OFST ~Kpog “plleg ‘SplVAapy[-oUllT jo Toqunyy ‘saggy avvloyjoppydoy fo sabopuaddy Jo aunjvjowowoyy CLASSIFICATION. Tae sub-kingdom Annulosa, to which the Crustaceans belong, is, according to the commonly accepted arrangement, one of the primary divisions, and in the number of its members by far the largest division, of the animal kingdom. Its most conspicuous character is that which is expressed by the term annulose, its members being composed of a variable number of more or less distant rings or body-segments (technically termed somites), arranged in longitudinal series, one behind the other. Besides the Crustacza, a group of which forms the subject of the present memoir, it contains several other important classes, the most familiar of which are the ANNELIDA (worms and leeches), ARACHNIDA (mites and spiders), and the Insxorva. The Crustacea, in their typical forms, are very distinctly segmented, the number of somites being variously reckoned at twenty or twenty-one; some of this number of segments are, however, in almost all cases suppressed, and not recognisable except theo- retically. Some or other of the somites almost always carry appendages adopted for mastication, locomotion, 16 BRITISH COPEPODA. and other purposes; and respiration is usually carried on by means of branchie or gills. There is always an external skeleton or ‘crust’? composed of a hard calcareous or a more flexible ‘* chitinous”’ material, from which investment the class derives its name. All, or almost all, the Crustacea pass through a series of metamorphic changes before reaching maturity. The Crustacea are divided into several sub-classes, the most important of which are the CrrRIPEDIA or Barnacles ; Matacostraca, including such animals as crabs, lobsters, shrimps, sandhoppers, and woodlice; and the Enromostraca, one order of which forms the subject of this monograph. The HEntomostraca are mostly very minute animals, the vast majority of living species varying between one fifth and one fiftieth of an inch in length. Some, however, are much larger, reach- ing a length of an inch oran inchandahalf. The Ento- mostraca are somewhat difficult to define in a way at once accurate and characteristic. The following is Professor Huxley’s statement :—“‘ In the Entomo- straca, if the body possesses an abdomen (reckoning as such the somites which lie behind the genital aper- ture), its somites are devoid of appendages. Moreover, the somites, counting that which bears the eyes as the first, are more or fewer than twenty. There are never more than three pairs of gnathites. The embryo almost always leaves the egg in the condition of a Nauplius ; that is, an oval body, provided with two or three pairs of appendages, which become converted into antennary organs and gnathites in the adult. This division of the HEntomostraca comprises the OLASSIFICATION. tf Copepoda, the Epizoa, the Branchiopoda, the Ostracoda, and the Pectostraca. **'The Coprropa.—In these EHntomostraca, which come nearest to the Hurypteride, the cephalic shield, which is discoidal and not folded longitudinally, is succeeded by a certain number of free thoracic and abdominal somites. The antennules and antenne are large, and, as in the Hurypteride, are organs of loco- motion and sometimes of prehension. The anterior thoracic members are converted into foot-jaws; the posterior serve as paddles, the limbs of each pair being often united together in the median line, as in Inmulus. The embryo leaves the egg as a Nauplius.” CHARACTERS OF FAMILIES. 1. CALANID#.—Body elongated; abdomen distinct from thorax; anterior antennz long, 24- or 25-jointed, that of the male, on the right side only, partially thickened and geniculated ; posterior antenne large, and usually 2-branched; mandible-palp usually 2-branched. Both pairs of foot-jaws large and well developed, many jointed, marginally setiferous. First four pairs of feet 2-branched, outer branches 3-jointed ; fifth pair similar to the foregoing pairs, or much modified (especially in the male) and unlike on the two sides. Ovisac single. 2. MisopHRIIDz.—Like Calanide, but that the anterior antenne are composed only of 7—18 joints, and are much shorter than the cephalo- thorax; robust, and in general build decidedly cyclopoid. 3. CycLoPpip.—Cephalothorax ovate and usually much more robust than the abdomen; anterior antenne seldom longer than the cephalo- thorax; those of the male alike on both sides and modified for the purpose of clasping; posterior antennz unbranched. Palps of mandi- bles and maxille usually well-developed. Foot-jaws mostly less deve- loped than in Calanidz. First four pairs of feet as in Calanide ; fifth pair rudimentary, alike in both sexes, and usually 1-jointed. Ovisacs two. 4. NoTODELPHYID&.—Fourth and fifth body-segments of the female usually coalescent, swollen dorsally to form a matrix or covering for the ova after their passage from the ovarium. Anterior antenne short, 5—15-jointed; posterior unbranched, 3-jointed. Mandible-palp 2- branched. Foot-jaws and swimming-feet like those of Cyclopide. Fifth pair of feet rudimentary or altogether absent. No external ovisac. 5. Buprorip#.—Body pouch-like, not distinctly segmented. An- tenne rudimentary, anterior 2- or 3-, posterior 1- or 2-jointed. No mandible-palp. Mouth-organs minute; maxille and foot-jaws short, broad, and adapted for chewing or grasping. Feet very small, papilli- form, 2-branched; no external ovisac; abdomen very small, furcate. All the appendages of the body very small and imperfectly developed. 6. HARPACTICIDZ.—Body sometimes complanate, but usually cylin- drical; abdomen not sharply separated from the thorax. Anterior — antenne short, 4—10-jointed, length scarcely exceeding that of the first CHARACTERS OF FAMILIES. 19 somite; those of the male modified on both sides, so as to form clasping organs. Posterior antenne 2—4-jointed, bearing a small secondary 1—4.jointed branch. Mandibles provided with a palp, which may be either simple and very minute or larger and 2-branched. Maxille composed of a setiferous grasping segment and a more or less complex laminar palp. First pair of foot-jaws jointed, with several marginal setiferous processes ; second pair usually (not always) forming a strong prehensile hand. First four pairs of swimming-feet 2-branched, first pair usually unlike the rest, and converted into a prehensile appa- ratus; second, third, and fourth pairs alike or nearly so, and adapted for swimming; fifth pair foliaceous, larger in the female. Ovisac single, very rarely double. 7. CoRYC#1ID#.—Body subpyriform ; abdomen elongated, much nar- rower than the cephalothorax. Anterior antennz 5—7-jointed, alike in both sexes, short; posterior simple, 3—4-jointed, forming a strongly clawed, prehensile hand. Mandibles, maxille, and first pair of foot-jaws minute, destitute (or nearly so) of palps. Posterior foot-jaws prehen- sible, and, in the male, powerfully clawed. First four pairs of feet adapted for swimming, 2-branched. Fifth pair rudimentary, alike in both sexes, rarely absent. One median eye, and usually two large simple lateral lenses. Ovisacs usually two. 8. SAPPHIRINIDZ.— Body either elongatedand subpyriform or broadly ovate and complanate; cephalothorax subovate and much broader than the abdomen, which may be either broad or elongated and subpyriform. Anterior antenne 5—7-jointed, alike in the two sexes; posterior simple, clawed or setose at the apex; mandibles small, subulate, or very feebly dentate; maxille small, and attached to the base of, or near to, the mandible. First pair of foot-jaws setiferous at apex; second pair clawed in both sexes, but much more strongly in the male. First four pairs of feet 2-branched and adapted for swimming; fifth pair small, usually l-jointed. Ovisacs two. 9. ARTOTROGIDZ.—Body broad, complanate; abdomen short, but distinctly separated from the cephalothorax. Anterior antenne short, 9—20-jointed, those of the male often modified to a small extent for clasping ; posterior short, 3—4-jointed, secondary branch (when present) 1-jointed. Mouth produced into a short bell-shaped, or into a long, tubular siphon. Mandibles stilet-shaped, simple or provided with a slender, filiform palp; maxille composed usually of two setiferous digits; first and second pairs of foot-jaws simple, 2—4-jointed, strongly clawed at the apex. First four pairs of feet 2-branched (fourth pair rarely 1-branched) ; fifth pair rudimentary or wanting. BRITISH COPEPODA. 20 ‘snunpno0pnas qT PAA e ALB LEASe) 188) 8 Aj eF0/OK8K0 6 (aia 'a/8 ich p/RS)Aia 0M. vice .as8)in.oh a lasane wi eligi a SEMIN eae peyutof | azoreysod "DI]AIU0T 4 + -OMY4 jo youraq c | el ia \ eae Ea MBLOOJ LOMOT pezutol ate ae fica 0 u0T40d Teorde eed { Aueu | ‘pozeytp jemaoujo f4 < Sa Ae ared poses jo yooy Surmumas at ‘ poqutol-om ; : ia eR ge jo uted qsay Rivets Pee jo Youraiq .ouUt ‘aoppupy __ 7OaNy enuin 5. Se eR, cee aoe) ‘ ATQOUN4SIp SseT 20 b> SNUT lequeutipn.t } | orour oyeur oy} wt ee 3 = SIMOpd DAT teeter acer certneerteeenies “= paquof-oo.yy] AS a 25 *"MAININIINAN IM T****eee08 Seer ervenees oy4 ul Te[LULISSTp a. i) nyjajuodp.n gy qouviq suo Jo posodutoo dye “I orarpuwen 5 = “D.NBD0IDULOUP****** ie ce mee soqourig OM} Jo posodmoo Eee sired qy.anoy pur && “SC ORE OID Aten RISA a A ajtsueqezd-uou ) o[euL UL fr ‘parqy ‘puooes Jo 8 “1 Tenor qooy Jo ared yay ‘ peqzutol-90.144 | oO your. 124no0 “99 Bodo AQUA apistayoa x Se Re Bil J DUDUMQOTT eee erence a[isueyead {4801 044 oTUN Test aieaeaeet ee eninge Ee ee porouerq ong ‘Surpooord og oxy) * PoPMTOL-eaxqg = Apxwou to ogre ‘HW CINVIVO—'T ‘me, VUHNAO HAL FO SISdONAS 21 OF THE GENERA. SYNOPSIS “ppoo0waquyy CeCe e eae eee ete der emt m eH EHH eee tree dee eaeeneseHreeeeeeneteeeses vee aceereneee eee rere earecvesons snuos YSTFLAg, 9uo Tuo SuIeyu0KD ‘Ww a1woudaAg—'¢ ‘weqT “ppoouprosy ttt Bin pve wlevarnjsiv/ain/atee s(e'¥ uleid'e aa avait’ viuiele/a Weisle\e wieiaversiaiu slates eioie niottie state SWisipewpeiee sees Syeisrervieynie sleitisinssie Saar EE RTT ONC) % ‘sn.oydo.sajgdoo,y"SUOISUAx9 OYI]-SUIM OFUL poonpord SPUNULGES O1IOBL *) Ur suryeutuE ‘ Pesce -oy}-oTeydoo jo ulsieu | -107 wuUSZUR a duo au ee a CEL Og (ee a aL enlaagscsuntees 2° E08 eiduiis ) [esaop {sMvpo yno}s OM4 - LOT.10980d, ee jo r sorortt) ee Fe ree ei ets eae Te | ‘semen f awed yay | peutoquy shydjapozo xy JOS J.LOYS [VLOAOS J OMy © squtot pue ‘smBhidowogy ices Ruse ealvote yh ine ae snntienin ier rae SCO aden tre "--yommiqeno) “ttf Desens ‘WH CIAHATAGCOLON—P ‘wey ‘pundopolig'****: jeotpuryfo ‘poqyutol-se149 10 -oa4 490} JO ] | camnoydoy dor ores iesebeee nsec snosoerjog) Hd TE “Furof euo 1 ae Pua Hoe d TOURAG-OM4 “DU0YyUy) Pee ee rete e re erent nesses seers seseseeees Cor ee ee eevee rensvssanses sjutol ine djed-oqipueyyr ‘sdopalio Bravalstovopetwie! vl svel Sis) sfatevojayal sare’ syereteisvaseroa,wuaveraverrisreleleiaeateys opisuoyoud q0u mel-400} IOMOrT ‘SJUOULLTY [VITOURAG OM} SULIvOG yO) CLO FF SMUD [VUIULIO} oyVULOUN YIM ‘opisueyoud ) oporoqny v 07 poonpos ‘AareyuoUIpnA ‘HW CIdOTOAQ—'E “Ue, "DIUtadary je! hed xo) Neha (Loy id ale argo vuueqyUe Lo1to}sod Jo qouvaq Arepuooes § pozutol-uoeses ) ‘sdojohoopnasg'**'*"*"*"*" poqurol-om4 | RHO Ase BvUUeZUR LOrteysod Jo youvrq Arepuooes ‘ poyutol-uw904y31e—u90}x18 f were Ms “piwydosupy’*: ttt tert poyurol-x1s J ‘W CIIAHAOSIP—'Z ‘Wey BRITISH COPEPODA. 22 ‘Apa hey ts centers erannadar tases poequtol-oay pedojesop TToM sael-400F Jo | euuoyUe } pumosoupogr tees poamot-ony ared ys.g ‘ poqutof-o0aq} 10 -0a4 ee i x putes ee ee I : ‘pypodaBuorg ehcrt rca ei eRe < Rr Gere are poqurof-xts 10 -aay J Permofeeryy [Jo ane ZAUIVBOE See nawenses esi hne sesene Pence tere aceesseesseene Cece eee eseeseeteeecerene peasevcers SOM veces poyutol-omy J ‘WH NIIGAdIONOT— '[ “Wry-qng pwauay fo sisdouliy "(p) muryayuaggr poyour.iq-OM4 djed-ojqrpuvut =) =poyes 7} | £ pomeyo | -moyTa JOOF YSAY ‘(c)aoumndumooyzumg " popouviq-ouo ) ATyoojsodut ‘posury } ‘poqyutol | jo qouraq | -eo1q9 IOUUL (1) omoyondmyy’** seo yeorde oyevur0UN ‘suo.14s YAM popraoid puv) 10 -oma ‘puvy smel-300; oyeu1omn : WE) OTT Fe taal ee eo “--poqurol-004} ) puw Surmtoy | ey uorsuoeyerd | you ynq : : ANGIE OULD Gres Bootes cna recess Spares eer esse taecomeae ste ass poyarol-omy | coy poydepe | ‘sassooo.id : esas a suvel-400} Lou SNLO.LOFIJOS ea Td "(e) aunmowmhap sitet uss Ue SEARS Jopudys poyesuoy | yeuLoceut tae poqurol-ou0 you SuLIvoq (3) vumpyjaowog’'********** ULLOFIT[OULey puw peor SCG LARUE Go pee aE nee aa OIE Seis mereeereeees DUB POMBO [NJIoMod wv Sururtof ) (i) CaO TE Tg (Ne aC RRL oA teen ela i onenissahincenpenenankonse*e HTINDG pad aOUs) ‘savjvunf-qny f sisdouliy ‘E CIOILOVAAVA—'9 ‘WR, 3) o THE GENERA. OF SYNOPSIS PET CON CULT GTI) pS aa re eR A A eS peyutol-omy é s) SEAS aL En ae ea Oe cee ee re Seer a! Pegi MEO apie Soa ‘sapojay()’**'** 49S MOT B OF poonpo. 0 ‘oynUTUE djed ofqrpuvu ‘ pequtol-omy ‘qoue.rq “DULOSO.UphYyUpy tt ttt tt te se teen eens meses nogutol-oa1yy 19jNO Y}. UL 109.1048 ‘DAyIOSAyT "2498 OPUS 9LOUTH TO OMY xodev oY} 4v SuLtveq : | ‘aguoydony "METS OYeUIOUN Su014s ant ‘poyurol-omy ‘pozyesuojo Cele Oct Sas pete icte yaa poten i \ jo Woursq 19uut ‘pyjahayyyy ‘+ £Tao yatol euo Jo pesoduioo ) ‘ poypuriqun t aed Y4INoF Jo youv«q touUt ‘snoopsoug’'**"''**"** OM ‘ (pozutol-omy Ajore1) poqgutol tee ae to -om, | 799449 ‘poyesuojo ATTensn ‘snyduno0yzung*"*"*"* GEOG 91a) ) Lamune ee ui J 5) ‘W NITLANVOOHINVO —'G “urey-qng “pyjayuagg'***' neseeyeeeess oq uo l-o91q} >) euujUe LOLLe4sod Jo youvaq Arepuooes { peyutol-90.143 OT a * poequtol-euo ‘T[eurs joo} SULUIUITAS yo ated 4s. VE AEE) ei aie la aus ea eecceie RS Sy Soi Rtgs eens Youerrq 1943no ULyy 1aSU0T jo ouraq rouUy pogutol-om4 ‘pypanjage bape atpetehcnasagts uit seecucn pause cane-urees ‘qoueaq 10qN0 WeYY 104.10]8 ‘HY NITTRHNGALQ—'f ‘wey-qnue ‘auowhuy Pee eeeee OC a ee re PO eee ee ee reer eee ne senses ete eeroeesaes eee ereees snu0ds oto ATuo SUIBITOLD ‘WH NINOWAWY—'€ “urey-qng “pUuoszlaqoay meres pnoqurol-omy ) ee ee dee Sierra oe vuuozyue 1o11e4sod Jo youvaq Arepuooes ‘ poqutol-ooryy \ yoy Jo ared DEP AL Poqaro, {SALE JO sopouRAg YO ‘adwaqnny tenes Peet ee ae eereesersene ee Cie[ele sein (sk) Viale 6 Biwi Silas Gie/niele s s\olee bine) ale deg tess . somite , ‘WH NIIGIHOV],-—"Z ‘Wry-qng BRITISH COPEPODA. 24) “uuneppyyaqnag seers SATOMIBl [VIVOUBIG SULIvaq ‘weurmel podeys AT AV[NSeLIt OM4 jo pesoduioo died-orqipuryy ‘ohpr tases ee eeeesees seeeee eoesene Pees ecw neeens soTouR.rg pozurol-at0 OMY Lipa ‘qutof eseq e ‘WH NIAG[—'6 “UR “qng “UWNIPY]]00L0 J ee ee ee ry eevee eee eae reee OCP e oe T SOHO HEHEHE EE OE eeeeeseres eeeteeree POORER ROE oe H EOS s88-onTOS euo ATO SuUIvyuOH ‘® NIIGITIGNUOG—'S “Wey-qng "SNOT i ir POR e eee EEO E HEHEHE ESE OEHEEH HOE ESE HEHEHE HEHE HEHEHE OHHH EE HOE EEE EES bee eoeens peeeee szutol om4>) jo JouUt >) es] | Sem jo |e ‘snpphsdohyy vere eee e ease eevee seseeses Pease ee resseseeeeese seeees OOOO dee eeseaeeenss ‘9SOJOST ‘gjduris dyed a[qrpueur \ pesoduios a Pe ao A haa ‘qutof ouo J A age ee “pypooaysa jy etree We aback BepReC ane nihatiatenecueareais payouraq-0m4 tol qomo B bo ‘unpyjag'’’ poutds A[su0148 pue “UIALOJIO[eJ-qus “poyesuoye qooy Jo ared qouriq —) 3. = qayy fyutol ysay oq 19yn0 FO le =p HLS LLTN OY UDITTAY Ug (i ene a ad Big ne BASES EISEN S “'** snosovrfoy J Uey} tasuoT Youu you ¢ yutol e_pprur = : ‘ pequrot \ soqouRig 5 “SLugsoy Te Ree en gasity wait i rin vals ee xin 5 aga nig ate ai a nM poyeSuoo Apyv0a8 J “201 | q30q eB Ate ‘snoyond.o yy De aioe santas Kua ks aa SAAC ORE Eero te SORA fade ee cabin alae an anions poqurol-omy | @ ‘W NIOILOVAUVH—— 2, “‘Wej-qng ROUEISOIU CHIN po ce cial al areca eons ee te gor Cea cir ene eeesecoes poqurol-se143 qooy jo ared 4ysay jo Touvaq 109nGO ‘sndyayohqong esi Sa ralC BISA SIRTET ETE alee oo OISTa: ULS) Cas ois Cie ai shete ololelnesiecer Terra SHOR aA Sad oaEOaaAOnGOSA poqurol-om4 ‘H NIGONNVN—'9 “WRy-qng 25 SYNOPSIS OF THE GENERA. Gy ONL Tai) | le aan a ae pozurof-anoj . euusjur 1o11e3sod ‘ pedvys-[eq pur 4.21048 seni one “puaordopahig ee pequtol-oo.144 f peonpoad ynour jo a "PULogsoUajog eeeesece Cree re eeeeoee sone Corer eesree veces voc eeeves xvL1oyyoreydoo oy} ueyy rasuoyz) : soTOURLG eee aed YAtnow ‘snuodshg ses0eseneenne steer rewemeerens Pov eeeeeeneseceveceveres Cece ee seecerceccereeseereceseneees eevee none . Aja yourrq oo ‘HAINOULOLAY—'6 “Wey ‘snbpomoyovy seevees tee ee veer eeeens veeveveee eh enceneoveens seeernees teversoeveeces tevenseers seenerenns treererseranttgS YStqLIg, otto Ayu0 surequOD ‘W CINIAIHddVO—'g "Wey ‘snaohwog AISCUOUCUUrT Ii Pececeevons aseraTaralWieleyesmeevelstate vie Sele erty: (syn clels pedojeaop-]jom SULI.1O-FINOU OY} [[V puUv VUUSyU .LOLIOySOg 0) ]VA4SUOTT re POCO mee eee eos nee Cee eer eee oeeeeneeeoeeeseooe quetoyep j ‘WUIWOLMOO—'Z, “WRT ” LIST OF MEMOIRS REFERRED TO IN THE TEXT. AttMAN, G. J. Description of a new genus and species of Hnto- mostraca (Ann, and Mag. Nat. Hist., vol. xx), 1847, Barrp, W., M.D. The Natural History of the British Entomostraca (Ray Society), 1850. List of Entomostraca found in Berwickshire (Trans. Berwickshire Nat. Field Club, vol i), 1834. Arrangement of the British Entomostraca, with a list of species (ibid., vol. 11), 1849. . History of British Entomostraca (Mag. Zool. and Bot., vol. i), 1837. On some new genera and species of British Ento- mostraca (Ann. and Mag. Nat. Hist., vol. xvii), 1846, Borck, AXEL ... Oversigt over de ved Norges Kyster iagttagne Copepoder henhorende til Calanidernes, Cyclopi- dernes og Harpactidernes Familier (Scerskilt aftrykt af Vidensk.-Selskab. Forhandlinger for 1864). Tvende nye parasitiske Krebsdyr. (ibidem, 1859). Nye Slegter og Arter af Saltvands-Copepoder (ibidem, 1872). Brapy, G. 8., M.D. Reports of Deep-sea Dredging on the Coasts of Northumberland and Durham—Pelagic Ento- mostraca (Nat. Hist. Trans. Northumberland and Durham, vol. i), 1865. On the Crustacean Fauna of the Salt Marshes of Northumberland and Durham (Nat. Hist. Trans., N. and D., vol. iii), 1868. Description of an Entomostracan inhabiting a Coal Mine (Journal of Microsc. Science, vol. ix), 1869. A list of the non-parasitic Copepoda of the North 98 BRITISH COPEPODA. East Coast of England (Nat. Hist. Trans. Northumberland and Durham, vol. iv), 1872. On the Zoology of Hylton Dene (Trans. Tyneside Nat. Hist. Club, vol. vi), 1864. BRADY, G.8., and Ropertson, D. On Marine Copepoda taken in the West of Ireland (Ann. and Mag. Nat. Hist., ser. 4, vol. xii), 1873. Report on Dredging off the Coast of Durham and North Yorkshire in 1874 (Brit. Assoc. Report), 1875. BUCHHOLZ, REINHOLD. Die zweite deutsche Nordpela in den Jahren 1869 und 1870. Cuavus, Dr. C. ... Beitrage zur Kenntniss der Entomostraken (Erstes Heft), Marburg, 1860. Die Copepoden-Fauna von Nizza. Ein Beitrag zur Charakteristik der Formen und deren Aban- derungen “im Sinne Darwin’s,” 1866. Das Genus Cyclops (Weigmann’s Archiv), 1857. Die frei-lebenden Copepoden mit besonderer Be- riicksichtigung der Fauna Deutschlands, der Nordsee und des Mittelmeeres, 1863. Neue Beitrige zur Kenntniss parasitischer Cope- poden nebst Bemerkungen itber das System derselben, 1875. i bE G 2 Wis 4 Pb alae Crustacea of the United States Exploring Expedi- tion, 1855. FISCHER, Dr. SEBASTIAN. Beitrige zur Kenntniss der Entomostraceen (Abhandl. der Konig. Bayer. Akad.der Wissensch. Bd. viii), 1860. Fric, Dr. ANTON. Die Krustenthiere Bohmens, 1871. Goopsir, H. D. On several new species of Crustaceans allied to Saphirina (Ann. and Mag. Nat. Hist., vol xvi), 1845, (GUNNER: rice. Act. Hafn., 1765. Hzuuer, C........ Untersuchungen iiber die Crustraceen Tirols (aus den Berichten des Medizinisch - naturwissen- schaftlichen Vereines in Innsbruck), 1871. Rese Mc sce Observations sur des Crustacés rares ou nouveaux des cétes de France, troisiéme article (Annales des Sciences Naturelles, 5me sér., tom. 1) 1864, JURINE, Louis... Histoire des Monocles qui si trouvent aux Environs de Genéve, 1820. Kroyer, H........ Karcinologiske Bidrag (in Naturhistorisk Tids- skrift), 1846—49. LIST OF MEMOTRS REFERRED TO IN THE TEXT. 29 J: Dict. Se. Nat., xiv, Art. Entomostraca, 1819. LILLJEBORG, W. De Crustaceis ex ordinius tribus, in Scania occurrentibus, 1853. De under Svenska vetenskapliga Expeditionen till Spetsbergen 1872—1873, derstades damlads Hafs —Entomostraceer (Ofversigt af Kongl. Vetens- kaps Akadamiens Forhandlingar, 1875). Lussock, Sir JoHN. On some Oceanic Entomostraca collected by Capt. Toynbee (Trans. Linn. Soc., vol. xxiii), 1860. Notes on some new or little-known species of Fresh- water Entomostraca (Trans. Linn. Soc., vol. xxiv), 1863. Description of eight new species of Hntomostraca found at Weymouth (Ann. and Mag. Nat. Hist., vol. xx), 1859. On Arctic Calanide (Ann. and Mag. Nat. Hist., 2nd ser., vol. xiv), 1854. MILNE-EpwaRrps. Histoire Naturelle des Crustacés, 1834. MULuer, O. F.... Entomostraca seu Insecta testacea que in aquis Danie et Norvegie reperit, 1785. Zool. Dan. Prodrom., 1776. Norman, Rev. A. M. Last Report on Dredging among the Shetland Isles (British Association Reports), 1868. Report of the “ Valorous” Expedition (Proceedings of Royal Society, 1876). Puiuierl, Dr. A. Fernere Beobachtungen uber die Copepoden des Mittelmeeres (Weigmann’s Archiv), 1843; also memoirs in the same publication in 1839 and 1840. RovussEL DE VAUZEME. In Annales des Sciences Naturelles, 1834. SUS 6 6 eee Oversigt af de indenlandske Ferskvandscopepoder, 1868. TEMPLETON ...... Transactions of Entomological Society, 1837. THORELL, T....... Bidrag till Kannedomen om Krustaceer, som levfa i arter af Slegter Ascidia, L. (till K. vet. akad. inlemnad d. 14 September, 1859). WEPANIN ® 5...:.. Reise in Turkestan, von Alexis Fedtschenko. Crus- tacea, pars 1, 1875. Van BENEDEN. Recherches sur la Faune littorale de Belgique, Crustacés, 1861. Westwoop,J.O. Partington’s Cyclopedia, Art. Cyclops, 1836. Wuitr,Apam... Popular History of British Crustacea, 1857. 6) CLASSIFICATION OF THE BRITISH COPEPODA. Sub-Kingdom.—ANNULOSA. CLASS.—CRUSTACEA. Sus-Ciass.—ENTOMOSTRACA. Legion. LOPHYROPODA. Order.—COPEPODA. Section 1 —Gnathostoma. Families. Sub-families. Genera. . Calanus. Metridia. . Pseudocalanus. . Candace. . Dias. Temora. . Diaptomus. . Isias. L . Centropages. 10. Parapontella. ; 11. Pontella. L 2. Pontelline ...... 12. Anomalocera. 2, Galanin: 5.0.02. 1. Calanidz.......:. 4 CO CONT Or OO DOH . Misophria. . Pseudocyclops. . Cervinia. . Oithona. . Cyclopina. . Thorellia, 1 2 3 A 2 PR VCLOPLOD yrivsins snide dunshinost's sisal Gaia iag seer 3 oe 4, Cyclops. 5 1 2 3 4 5 Be MASOP REGED as icsesnncewnaceceas ves duce repens { | | . Lophophorus. . Notodelphys. . Doropygus. . Notopterophorus. . Botachus. ' ; ; } } ‘ d . Ascidicola. 5, BUprorvide 305 shinee anen- hor oeswnen eae eee 1. Enxterocola. . | CLASSIFICATION OF THE COPEPODA. Families. Sub-families. | 1. Longipediine ... & Tachiduns: 6... ! 3. Amymonine......... U 6. Nannopine ...... 1 93 rc CO CONT OU OO DOS Genera. . Longipedia. Hctinosoma. Zosime. Bradya. Tachidius. . Euterpe. . Robertsonia. . Amymone. . Stenhelia. | 4, Stenheliine ...... 1L | Ameira. . Jonesiella. . Delavalia. . Canthocamptus . Attheyella. . Mesochra. . Tetragoniceps. 5. Canthocamptiine 17. 6. Harpacticide ... ¢ | 1s Diosaccus. Laophonte. . Normanella. . Cletodes. . Enhydrosoma. . Nannopus. . Platychelipus. . Dactylopus. . Thalestris. . Westwoodia. 7. Harpacticine ...4 27. . Harpacticus. . Zaus. . Peltidium. . Porcellidium. . Idya. . Scutellidium. . Cylindrosoma Ilyopsyllus. ol (incertz sedis). , 1, Coryceeus. DEERE RNGIS ree cna sce sss viceccnssesveuseteenesnednans { Bi Nee malas REMAP oo. 5 cc ics co ancescestveseuerervecdvavestens 1. Lichomolgus. PEPEMELOUEOZIOCS .. cide sc ccs canvveevsrsaeceguevetens HOD DO ES . Cyclopicera. . Artotrogus. . Dyspontius. . Solenostoma. eh ee ged t ‘ BRITISH COPEPODA. Sub-Class—ENTOMOSTRACA, Miller. (GnatHopopa, H. Woodward.) Orprr—COPEPODA. Section J.—Gnatuostoma, Thorell. Family 1. Catanipa, Dana. Bopy elongated ; composed of from ten to twelve segments. Abdomen nearly cylindrical, much nar- rower than the cephalothorax and prolonged at the posterior extremity into two more or less cylindrical caudal branches. First segment of thorax often anchylosed with the head; fourth and fifth segments also often coalescent. Head only rarely divided into two segments. Anterior antenne very long and composed of twenty-four or twenty-five joints; that of the right side in the male often modified for erasping. Posterior antennze large, composed of a basal joint from which spring usually two branches, the primary branch consisting of two, the secondary 3A BRITISH COPEPODA. of several joints. Mandibles strongly toothed at the apex, palp (usually) two-branched. Maxille strong, and provided with a many-lobed palp. Foot- jaws strongly developed: first pair very broad; the basal joints having on the inner margin wartlike processes from which spring long ciliated bristles; the distal extremity divided into three short joints which are thickly beset with strong and long ciliated sete: second pair longer and more slender, basal portion forming two long oval joints; apical portion usually 4.—6-jointed. First four pairs of feet 2-branched, the outer branches always three-jointed. Fifth pair either hke the foregoing, or much modified, unlike on the two sides, and in the male forming clasping organs ; a heart is present. Hyes either median and stalked or paired (lateral) and sessile ; in the latter case being often coalescent and composed of several lenses. Sexual organs in the female symmetrical, in the male asymmetrical. Ovisac single; borne in front of the abdomen. This definition is framed so as to include the species belonging to the two families Calanidée and Pontellidz as described by Dr. Claus. There being, as I think, no sufficient ground for separating the latter as a distinct family, I here follow Dana and Boeck in con- sidering the whole as one family, comprising two sub- families Calanine and Pontelline. The characters which chiefly distinguish the two groups are those of the eyes, footjaws, and anterior antenne, but Claus has pointed out that the genus Centropages exhibits a transition as regards tbe eye, while Centropages, —_ il ial tt ame ‘ : ; d CALANIDA. on Temora, and other genera have characters very similar to the Pontelline group in the antennz and footjaws. The chief points of generic distinction are to be found in the structure of the inner branches of the swimming feet—more especially in those of the first and second pairs,—in the characters of the fifth pair of feet and of the mandibles, maxille, and foot- jaws. As regards the mouth organs the most noteworthy modifications are those found in Candace, where the mandible is remarkably slender and its palp much dilated, the maxille being at the same time of quite abnormal structure ; and in Dias and Parapon- tella where the apical portion of the lower footjaws is so much reduced in size as to be almost aborted. Specific distinctions have sometimes been founded on the number of joints in the branches of the swim- ming feet, but it must be borne in mind that this character is liable to vary with the stage of development of the animal. A table of such variations is given amongst the remarks on the genus Cyclops, and I hope, in an appendix to the second volume, to illus- trate from Arctic specimens in the possession of the Rev. A. M. Norman a somewhat similar process of development in Calanus. BRITISH COPEPODA. 36 Y peyatol | zo1104sod | [ ‘I]9IU0T + -OmMy | JO WOURIG 10 -ou04 = euUt ‘ poy3004 soqqrpueut MBlJOOF IAMOT egatol | -suvut o uorj4od [vorde | “DLOWAT, ee payer 4 OZIS [VULLOU JO J entre ae | ared ptooes jo = f Rear oes joo} SUIMIMITMS *‘poqyo04 | jo ared 4sag ‘soppUpy*''*** eee | jo La IouUtl ‘TLIOJI : Mtge ropes dy OSH . ur IeyUOWIpNt TJOULSIP S$9T IO | 198 eLOUl TLUL Oy} UL] | = ‘snwmo dng ee ee ee ee rr ee ee Deer eeeeveveve Seer eeeees eee pequrol-90.193 J eptis qystt ey jo bo 3 qyeqy ‘SOxXoS OM} | ch, BAPTA’ PA eo TGR CR ETTOOr Fey? fo} nyazuodn.w gq youraiq eo Jo posodutoo dyed oyqrpueur i | oy} UL Ie[IUIISsTp g 8 “puav0jnUoUp soTour.q OA Jo posoduroo ‘perma roM) sired qyAtnoy pue aE ‘SIUST eterna apisuoyord-tou o[euL UT a ‘pangs ‘puooes jo 53 . qooy jo ared yyy | : peyutol-90.194 PRET rats ncins de Rese PESTA Ses reteastat jo youriq 109n0 sabodouuap episueyord ‘paqutof-eery3 J L ‘snupyooopnasg 00" nin Glan @ Re asadiienns Aid =a Sr a uns re Meee eee eee tame as Bieter ete poqurof-eu0 ee ieee jo Youraq tout MAU DUUO IT conte trsass oe abvestnynenccvonsnsis erenauaid aia ae 4 ‘SOKOS a Teens ESE SEY ONTES | aed yazg yo 9003 | _qy0q UT aRTTE ‘smog wii cle coset ace ' peqouraq-om9 ‘Surpoooad o4} oxy ‘ pozutol-90144 L Aj.Lvow LO OYITV J WCINVIVO JO VUHNHSD HO SISONDVIG CALANUS. 37 Sub-family 1. Cautantnm, Dana. This sub-family is characterised by the presence of only one eye which is made up of several lenses; by the 24—25-jointed anterior antennz and by the long and slender form of both thorax and abdomen: rostrum slender, and usually, if not always, furcate. Genus 1. Catanus, Leach (1819). (Leacu, Dict. Sc. Nat., xiv, Art. Entomostraca.) (Cetochilus, Roussel de Vauzéme, Claus, Baird.) Cephalothorax elongated, slender, consisting of five segments. Head produced into an attenuated, forked rostrum. Hyes small, situated at the back of the head, near the middle line, and composed each of two lenses. Anterior antennz very long, composed of twenty-five joints; alike on the right and left sides in both sexes, and possessing no hinge-joint: those of the male are provided with thickened, club- shaped hairs. Posterior antennz two-branched, the secondary branch having four small intercalated median joints. Maxilla forming a broad laciniated plate, armed with strong marginal sete, some of which are plumose, and having attached to it two short and broad leaflike processes, which bear long branchial filaments. Mandibles large and strong, the cutting portion ending in a wide sharply-toothed mar- 38 BRITISH COPEPODA. gin; basal joint of the palp large and broad ; branches densely setose, one 4-, the other 2-jointed. Anterior footjaws broad and strong; posterior elongated, the terminal portion being divided into five joints; both pairs armed with numerous strong and long sete. Five pairs of feet adapted for swimming, two-branched, each branch being composed of three joints; in the male, however, the outer branches of the fifth pair are somewhat modified. Abdomen of the male 5-, of the female 4-jointed. 1. CaLANuUs FINMARCHIOUS (Gunner). Pl. I, figs. 1—12. Monoculus finmarchicus, Gunner. Act. Hafn., x, 175, figs. 20—23 (1765). Cetochilus septentrionalis, Goodsir. Edin. New Phil. Journ., 35, p. 339, t. vi, figs. 1—11 (1843). — _ Baird. Nat. Hist. Brit. Entom., p. 235, t. xxx, figs. 1 a—g (1850). — helgolandicus, Claus. Die frei lebenden Copepoden, p. 171, t. xxvi, figs. 2—9 (1863). Calanus finmarchicus, Boeck. Oversigt over de ved Norges Kyster lagttagne Copepoder, p. 8 (1864). _ — Brady. Nat. Hist. Trans. Northumberland and Durham, vol. iv, p. 424 (1872). — magnus, borealis, and elegans, Lubbock. Ann. and Mag. Nat. Hist., 2nd series, vol. xiv (Aug. 1854). Anterior antennze about as long as the body (figs. 2, 12), the twenty-third and twenty-fourth joints bearing, the one at the apex, the other near the middle, a long whip-lke hair which is ringed and densely ciliated ; in the male these hairs are more slender. Posterior antennez two-branched (fig. 3), the outer CALANUS. 39 branch consisting of two joints, the inner of seven, four of which are very short; the inner branch bears long marginal hairs along almost its entire length. The basal joints of the fifth pair of feet in both sexes are minutely serrated on the inner margin (fig. 8). The fifth pair of feet in the female are lke the preceding pairs, but in the male (fig. 11) have the first and second joints of the outer branch greatly elongated and are devoid of marginal hairs, the third joint being small, pear-shaped, and provided only with a couple of minute spines at the apex. The terminal spines of the swimming feet (fig. 10) are long, awl-shaped, and destitute of serratures or hairs. Tail sete about as long as the abdomen. Length of the animal, including tail setz, about one sixth of an inch (4 mm.). Colour variable, sometimes almost pellucid, at others yellowish or dark red; the body is often loaded with large highly refracting oil globules. This species is found, often in immense numbers, all round our coasts both in the open sea and between tide marks, more especially in the early summer months. It is essentially a pelagic species, loving the clear ocean and not often to be met with in any great numbers amongst weeds. Itappears to be generally distributed in the Arctic Ocean, the North Atlantic, and the Huropean seas, and I have seen specimens collected by Mr. Haton in the southern hemisphere, which are in no respect distinguishable from the northern species, though possibly identical with one considered specifi- cally distinct by R. de Vauzéme.* It has been said to * « Annales des Sciences Naturelles,’ 1834. AO BRITISH COPEPODA. constitute no inconsiderable part of the food of the whale. 7 The three species, C. magnus, borealis, and elegans, described by Sir John Lubbock (loc. cit.) from speci- mens taken in the Arctic Seas, seem to be founded, as pointed out to me by Mr. Norman, on different stages of development of the present species. Having had no opportunity of seeing the old descriptions given by Gunner and Leach, I here follow M. Boeck who seems to have examined the literature of the subject with much care. The conclusion is that Gunner’s description has been wholly misunder- stood or overlooked by modern writers ; his Monoculus _ jJinmmarchicus (which has usually been identified with the Temora longicornis of the present monograph) being really the species now under consideration, Calanus jinmarchicus. Leach’s genus Calanus was established in order to receive Gunner’s species, though the name has been used by recent authors (Dana, Lubbock, Claus) to include species wholly different. If this view be correct it is only right that the term Calanus should revert to the species for which it was first proposed ; the genus Cetochilus being at the same time discarded. Genus 2. Mutripia, Boeck (1865). (? Pleuromma, Claus.) Head separate from the first ring of the thorax, and produced into a cloven rostrum: fourth and fifth METRIDIA. Al seoments coalescent. Abdomen in the female consist- ing of three, in the male of five segments. Anterior antennz as long as the cephalothorax, 25-jointed in the female, in the male 20-jointed and furnished with a hinge between the seventeenth and eighteenth joints. Second pair of antenne as in Calanus ; mouth organs as in Calanus. First pair of feet smaller than the rest: both branches of the first four pairs of feet three-jointed ; fifth pair, unlike the others, composed of one branch only and dissimilar on the two sides; in the male formed for grasping. , The characters on which Boeck relies to separate this genus from Plewromma, Claus, are the complete separation of the cephalic from the thoracic segments, the 3-jointed branches of the swimming feet, and the absence of lateral eye-spot. It is possible that further investigation may show these distinctions to be un- founded, but the male abdomen as figured by Claus in the case of Plewromma is distinctly different from that of Metridia in being provided with lateral processes. M. Boeck, however, is wrong in stating the number of antennal joints in Metridia to be twenty-four. The real number is twenty-five, and in this respect it agrees with Plewromma. While this Monograph has been going through the press Mr. Norman has pointed out to me that the name Metridia (Metridium being already in use for a genus of Actinozoa) must be withdrawn, but as it seems doubtful whether Plewromma ought or ought not to be adopted as the generic appellation, I prefer for the present to let Metridia stand. A?2, BRITISH COPEPODA. 1. Merripia armata, Boeck. PI. II, figs. 1—12; PI. LVI; ties. £9,720: Metridia armata, Boeck. Oversigt over de ved Norges Kyster iagttagne Copepoder, p. 14 (1865). Paracalanus hibernicus, Brady and Robertson. Annals and Magazine of Nat. Hist., ser. 4, vol. xii, p. 126, pl. viii, figs. 1—3 (1873). Rostrum obtuse; anterior antenne (fig. 2) nearly alike in both sexes, slender, a little longer than the cephalothorax, thick at the base and tapering gradually to the apex; the nine basal joints (except the first, which is very large) are broader than long, the rest being from twice to thrice as long as broad except the apical one, which is very short: each joint bears on its outer margin one or two short setz (some of these being in the male developed into thickened rod-lke appendages), and the seven or eight proximal joints are each produced on the outer margin into a short median spine or tooth; the last joint has one long and two small seta, the penultimate one very long seta: in the male the antenna is twenty-jointed, hinged between the seventeenth and eighteenth joints (Pl. LVI, fig. 19). Both branches of the posterior antenne are stout and nearly equal in size. Mandibles (fig. 3) strong, with a largely developed, biramose palp. Second pair of foot- jaws (fig. 6) very slender. The swimming feet (fig. 7) have the inner branch very short, only about half the length of the outer branch, the last jomt of which is long and truncate at the apex; marginal and terminal spines very small, the latter (fig. 12) some- METRIDIA. 43 what leaflike and minutely serrated on the outer edge. Fifth pair of feet cylindrical, unbranched, in the male four- and in the female three-joimted; those of the female, however, much shorter than of the male, and having joints of nearly equal length (fig. 10) ter- minated by two or three fine short sete. In the male the first and fourth joints are much elongated (figs. 8 and 9), and the second joint bears a slender curved process; the foot of one side is also much more slender than that of the other. The inner branch of the second pair of feet in the male has the first joint very much excavated at the upper and inner margin, the lower margin of the excavation having alarge and strong spine (Pl. LVI, fig. 20 b) at the angle, and two smaller ones internally. Abdomen of female 3-, of male 5- jointed. Caudal setz short, scarcely half the length of the abdomen (fig. 11). Length, exclusive of the caudal sete,* jth of an inch (1°6 mm.). Arctic examples belonging apparently to this species, taken during the expedition of the “ Alert”’ and “Discovery,” and now in Mr. Norman’s possession, are much larger, measuring at least twice as much (4th of an inch). J am indebted to my friend Mr. EH. C. Davison, R.N., of Sunderland, for several collections of Entomostraca taken in the tow-net off Ireland and in other localities, and my knowledge of the present species is almost entirely derived from these gatherings, in several of which it occurred plentifully. The localities are as follows,—off the mouth of the Shannon; Galway Bay ; * Except where otherwise stated, the measurements of length are in all cases to be taken as exclusive of the tail sete. 4,4, PSEUDOCALANUS. off Loup Head; Dingle Bay; near Valentia; Rockall Bank; in lat. 51° 22’ N., long. 12° 25’ W., and lat. 53° 24 N., long. 15° 24° W. I have myself taken it, though very sparingly, in the surtace-net amongst the Scilly Islands. It may be noted here that in most of the Calanidee the apical spines of the outer branches of the swim- ming feet afford excellent distinctive characters, and, on this account, are carefully figured in the plates. The first swimming foot is, however, usually, if not always, destitute of a spine, its place being occupied by a stout hair or seta. Genus 3. Psnupocatanus, Boeck (1872). (Pseudocalanus, Boeck, Nye Slegter og Arter af Saltvands-Copepoder, 1872. Clausia, Boeck, 1864. Calanus, Brady, 1865.) Like the preceding except in the structure of the feet, which are composedas follows. The outer branch of the first four pairs is always 3-joited ; in the first pair the inner branch consists of only one joint, in the second of two, in the third and fourth of three joints. The fifth pair of feet in the female are alto- gether absent; in the male they form two very slender limbs, 5-jointed on the right, 3-jointed on the left side. The term Clausia, at first proposed by M. Boeck for this genus, had been previously used by Claparéde for a genus of parasitic Copepoda. It was, therefore, in a later publication, withdrawn by M. Boeck, the desig- nation Pseudocalanus being substituted. PSEUDOCALANUS. Ad 1. PsEupocaLanus ELonGatus, Boeck, Pl. III, figs 1—9. Clausia elongata, Boeck. Oversigt Norges Copep. p. 10 (1864). Calanus Clausii, Brady. Nat. Hist. Trans. Northumberland and Durham, vol. i, p. 33, pl. i, figs. 1— 11, 13 (1865). Body elongated, ovate, anterior antenne in the female (fig. 2) 25-jointed, the seventh and eighth (or eighth and ninth?) joints being coalescent, the rest eradually increasing in length and tenuity as they approach the distal extremity: in the male the number of joints is reduced to twenty by the coalescence of several, the seventh, eighth, and sixteenth joints (fig. 3) thus becoming much elongated; the two or three terminal joints are swollen at the distal extremity and contracted at the base, and in the male some of the other joints are also similarly enlarged ; the outer margin of the antenne is sparingly provided with short hairs. Fifth pair of feet wanting in the female ; in the male (fig. 8) they are long and slender, the left consisting of three cylindrical tapering joints, of which the middle is the longest; the right of five joints, of which the first three are nearly equal in length, the fourth shorter and the fifth quite minute and claw-like. The first abdominal segment in the female is much the longest and is tumid in front; in the male it is very short : abdomen 4-jointed in the female, 5-jointed in the male; the caudal segments very-short; tail setze also short, scarcely equal to half the length of the D A.6 BRITISH COPEPODA. abdomen in the female, still less in the male (figs. 1, 9). Length about sth of an inch (1°3 mm.). Colour yellowish or reddish yellow, quite transparent. P.-elongatus 1s a very common species, being dis- tributed all round the British Islands between tide marks and in the open sea. It 1s often met with in considerable numbers. M. Boeck points out that in some specimens, which he supposes to be females, there are traces of a fifth foot in a rudimentary stage. I at one time also held this belief, but am indebted to Dr. Claus for suggesting to me that these specimens are in reality immature males, and that along with the imperfectly formed feet there are usually also other signs of immaturity in the animal. The female must, therefore, be considered to be constantly destitute of a fifth pair of feet. 2. PsEuDOcCALANUS ARMATUS, Boeck, Pl. IV, figs. 1—11. Pseudocalanus armatus, Boeck. Nye Slegter og Arter af Salt- vands-Copepoder, p. 6 (1872). Body elongated (fig. 1); head quite distinct from thorax; fourth and fifth thoracic segments coalescent, and produced at the dorsal angle into a strong back- ward-projecting spine; ventral angle rounded off. Anterior antenne in the female stout (fig. 2), as long as the cephalothorax; 1st and 2nd joints large, and longer than the next following ten joints, which are short and broad; the 13th joint is about PSEUDOCALANUS. AW twice as long as broad, and the remainder are mostly somewhat longer in proportion to their width, except the last, which is very short; the whole length of the antenna beset on its outer margin with long and stout hairs, those of the last five or six joints being especially strong and transversely ringed. ‘The anterior antenne of the male (fig. 3) are more slender, and the joints beyond the middle much longer, the 18th to the 24th being especially slender; the organ is not nearly so densely setose as in the female. The posterior antennz and mouth organs do not differ materially from those of the genera already described ; the pos- terior footjaw (fig. 7), however, has the first two joints with only three marginal sete, near the middle of each joint. ‘The swimming feet are much larger and stronger in build than in the preceding species, and have their terminal spines (fig. 9) beset on the inner margin with large and widely separated teeth. Fifth foot of the male (fig. 10) even more slender than in the preceding species, the last joint bearing at the apex two small terminal sete, and on its inner margin a comb- like series of about nine or ten moderately long hairs. Caudal segments about as long as the last abdominal segment; sete nearly as long as the abdomen. Colour very dark brown; so opaque, indeed, that scarcely any structure can be seen until cleared by solution of potash. Length ;yth of an inch (2°55 mm.). My only examples of this species were dredged in a depth of fifteen fathoms, off Portincross, Ayrshire, and off the south end of the Island of Bute. A8 BRITISH COPEPODA. M. Boeck states that the inner branch of the first pair of feet consists of two joints; but after careful examination I have not been able to see any separa- tion into two segments. It is quite possible, however, that this character may vary somewhat in different individuals, as it certainly does in the case of Temora longicornis. It seems not unlikely that in very old specimens the separation of the segments may become more distinct, but in this case the individuals examined appeared to be fully grown and matured. Genus 4. Canpacr, Dana (1846). (Dana, American Journal of Science, ser. 2, 1846.) (Ifionyx, Kroyer, 1849.) Anterior antenne 23- or 24-jomted, that of the male on the right side geniculated, and having the median” joints only shehtly swollen. Posterior antennez stout ; the secondary branch having no median joints. Rostrum rounded. Mandibles twisted, narrow, ending in two stout teeth, the palp very much expanded. Maxille bearing a long styliform process, masticatory portion subtriangular. First pair of footjaws very strong, bearing long uncinate setz, second pair slender and small. [Fifth foot in the female composed of one triarticulate branch on each side, those of the male dissimilar, the right prehensile. Abdomen com- posed in the female of three, in the male of five segments. GANDACE. A9 1. CANDACE PECTINATA, nov. sp., Pl. X, figs. 1—12; Pl. VIII, figs. 14—15. Body elongated and slender; anterior antenns (fic. 3) as long as the body, 24-jointed, the thickened basal portion /-jointed, the remainder of about equal thickness throughout and extremely slender; third joint the largest, eighth to eleventh very short, seven- teenth, eighteenth, and nineteenth the longest, the whole sparingly setiferous: right antenna of male (fig. 1) very slender beyond the hinge-joimt and only slightly swollen in the middle ; joint next above the hinge of a smoky brown colour, armed with a crest or comb of large and strong deeply coloured spines; the joint immediately above this principal armature and that below the hinge bear dentated plates of the usual character (fig. 2). The posterior antenna is large and stout, the main branch bearing two and the secondary branch one terminal brush of about six long sete. Mandible-palp triangular, with two short setiferous branches (fig. 4) at the terminal angles. The basal portion of the maxilla (fig. 5) bears at its apex one very long and several shorter setz ; styliform process slender and carrying two apical sete. First pair of footjaws long and strongly armed; second pair slender (fig. 6). Inner branches of the swimming feet two-jointed throughout (fig. 7); marginal spines of the outer branches very small; swimming setz all densely plumose beyond the middle; terminal spine of outer 50 BRITISH COPEPODA. branch strongly pectinated on the outer and densely hairy on the inner margin (fig. 8); these spines and the plumes of the swimming setz deeply coloured. Fifth pair of feet in the female simple, three-jointed ; terminal joint long and curved, tapering to the ex- tremity, which is sharp and. twice dentated on the outer margin. Fifth pair in the male one-branched, that of the left side simple, four-jointed; the right having the last two joints modified into prehensile form (fig. 10). Last jomt of the thorax in the male produced at one side into a long spine; first abdominal segment produced in a similar way, but on the opposite side (fig. 11). Caudal segments very short; sete about aslongas the abdomen. Length of the animal ,;4 th of an inch (2°3 mm.). A very few specimens of this interesting species were dredged by Mr. Robertson and myself in June, 1873, on very hard ground and in a depth of about forty fathoms, south-west of the island of St. Agnes, Scilly. It appears to be quite distinct from any species described by Dana, Kroyer, Claus, or Boeck, though the female antennz very nearly agree with those of C. longimana, Claus. Genus 5. Dias, Ivlljeborq (1853) (Acartia, Dana, 1n part.) Body long and slender, head narrowed above and produced into a slenderrostrum. Abdomen consisting in the male of five, in the female of three segments. docalanus armatus 4 L DIAS. ot Anterior antenne, in the female, 20-jointed, armed with long sete, nodose, and (in the male on the right) geniculated. Primary branch of the posterior antenna much elongated, secondary branch short and 1-jointed. Labium very large, three-lobed, and setiferous, the middle lobe very broad. Mandibles as in Calanus. Branchial plates of the maxille small. Anterior foot- jaws largely developed and armed with many strong, uncinate setz ; posterior pair provided at the base with two large setiferous processes, the apical portion small. The swimming feet have the internal branch of two, the outer of three joints. The fifth pair of feet are one-branched, those of the male prehensile. Hye formed of several lenses. The genus Acartia of Dana includes, no doubt, not only some species of Dias, but others which are properly referable to distinct genera. The term Dias has been generally adopted for the following species, and I have therefore retained it here. 1. Dias tonetremis, Lilljeborg, Pl. V, figs. 1- 14. Dias longiremis, Lilljeborg. De Crustaceis ex ordinibus tribus, p. 181, tab. xxiv, figs. 1—13 (1853). — — Claus. Die frei-lebenden Copepoden, p. 193, taf. xxxiui, figs. 6—14, and taf. iu, figs. 1 and 2 (1863). — — Boeck. Oversigt over de ved Norges Copepoder, p. 12 (1864). — — Brady. Nat. Hist. Trans. Northumberland and Durham, vol. i, p. 35, pl. 1, fig. 14, and pl. ui, figs. 11—18 (1865). Calanus eucheta, Lubbock. Ann. and Mag. Nat. Hist., series 2, vol. xx p. 401, pl. x, figs. 1—6 (1857). By BRITISH COPEPODA. Head united with first ring of thorax, or only in- distinctly separated. Anterior antenne as long as the cephalothorax, the right of the male having nineteen, the left twenty-one joints; many of the antennal joints in both sexes much swollen at the apices, giving the organ a knotted appearance, the whole being beset with scattered hairs, some of which are excessively long: the ninth to the thirteenth joints of the male right antenna are much swollen to provide for the internal muscular apparatus, and the hinge is situated between the fourteenth and fifteenth joints (figs. 2, 3, 4). Anterior foot-jaw approaching in appearance that of Pontella, its numerous strong sete being armed with short rigid divaricating hairs. Posterior foot-jaws bearing on the basal joint a papilliform process which supports a single very long seta and three smaller ones; the second joimt has a single long seta which also springs from the summit of a papilla; the remain- ing joints are smaller and bear small marginal spines. Terminal spines of the swimming feet long, slender, sword-shaped, and finely serrated on the inner border. These spines are peculiar, for instead of having one or more small supplementary spines at their base, con- nected with the last segment of the foot by a movable joint, as is usually the case, the spine is, in this species, formed by a mere arched and pointed process of the outer edge of the foot (fig. 11). The fifth feet in the male consist each of a four-jointed branch, forming a pair of strong crooked and prehensile claws (fig. 13), the inner margins of which, especially on the right side, are pro- duced into wart-like projections, and the terminal joints TEMORA. OG are fringed with small spines or spine-like hairs. There is, however, considerable variety in the conformation of these organs. ‘The fifth foot in the female (fig. 12) ig small, three-jointed, the basal joint stout and bear- ing a single long seta, the next very small, and the terminal joint forming a long and slender curved claw. Abdomen very short, the first segment, in the female, being much the largest; caudal segments also short, about twice as long as broad: tail-sete rather longer than the abdomen. Length goth of an inch (1°3 mm.). Colour yellowish, whitish, or pellucid. Dias longiremis is found abundantly in the open sea and between tide marks all round the British islands; it occurs sometimes also in brackish water, but in that case is usually small and poorly developed. Genus 6. Temora, Baird (1850). (Cyclops (in part), Miller. Calanus (in part), Leach (fide Boeck), not Monoculus, Gunner.) Body elongated; head distinct from the thoracic segments; rostrum bifurcate. Fourth and fifth thoracic segments either completely coalescent or their separa- tion merely indicated by a furrow. Abdomen com- posed of four segments in the male, of three in the female. Anterior antenne twenty-four- or twenty-five-jointed ; that of the right side in the male having a hinge-joint and forming a prehensile organ. Mouth organs as in Calanus. Inner 5A BRITISH COPEPODA. branches of the first, second, third, and fourth pairs of feet two-jointed. The fifth pair are composed each of one branch, those of the male forming clasping organs. Abdomen of the female three-, of the male four-jointed. 1. Temora Loncicornis, Muller, Pl. III, figs. 10—19. Cyclops longicornis, Miller. Entomostraca p. 115, t. xix, figs. 7—9 (1785). Temora fiwmarchica, Baird. Brit. Entom. p. 228, t. xxviii, figs. 1 a—g (1850). — — Claus. Die frei-leb. Copep., p. 195, t. xxxiv, figs. 1—11 (1863). — = Brady. Nat. Hist. Trans. Northumberland and Durham, vol. i, p. 36, pl.i, fig. 15, and pl. u, figs. 1—10 (1865). — longicornis, Boeck. Loc. cit., fp. 15 (1865). — = Brady. Nat. Hist. Trans. Northumberland and Durham, vol. iv, p. 425 (1872). Diaptomus longicaudatus, Lubbock. Ann. and Mag. Nat. Hist., ser. 2, vol. xx pl. x, figs. ll and 12 and pl. xi, figs. 12 and 13 (not Mono- culus finmarchicus, Gunner) (1857). Body wide in proportion to its length, dorsal margin much arched, posterior dorsal angle rounded off, ventral produced and subangular. Anterior antenne (fig. 12) rather longer than the cephalothorax, twenty- five-jointed, the segments more attenuated and increasing slightly in length towards the distal extremity, the basal joint, however, being the largest of all; each segment bears two short slender hairs at its apex. The right antenna of the male (fig. 11) has a TEMORA. 5G movable hinge between the eighteenth and nineteenth joints, the last four joints being very long and apparently representing a coalescence of eight joints ; the inner margins of the joints immediately above and below the hinge are armed with finely denticulated plates; and the fourteenth to the eighteenth joints (both inclusive) are swollen, apparently to give more space for the powerful muscles by which the organ 1s moved. The posterior antennz and the mouth-organs do not differ materially from those which have been already described. Inner branches of the first four pairs of swimming feet two-jointed; those of the first pair often apparently one-jointed owing to imperfect division. The fifth foot in the female (fig. 16) consists of a simple, cylindrical, and rather stout three-jointed branch, the last joint being the longest and having two small lateral, and two apical spines of about equal size. The right fifth foot in the male (fig. 17) consists of a large basal joint to which are articulated two opposable claws, one of these bemg long, simple and curved, the other composed of two broader joints, and bearing at the apex two tooth-like spines and two short hairs: the left foot is three-jointed, subchelate, but unbranched. Theterminal spines of the swimming feet (fig. 19) are long and straight, with slightly curved apex and finely serrated inner border. The caudal segments (fig. 18) are extremely long and slender, quite equal in length to the whole of the abdomen, about eight or nine times as long as broad, and bearing a single short lateral spine on the external margin, about half way between the middle 56 BRITISH COPEPODA. and the distal extremity: terminal setae plumose, not quite equal in length to the tail segments. Colour brown. Length goth of an inch (1°3 mm.). Temora longicornis is one of the most abundant of the marine Copepoda. It occurs often in great profusion in tidal pools amongst seaweeds, and is likewise taken abundantly in the towing net in the open sea. It seems, in fact, to be ubiquitous in the British seas. ) 2. Temora vetox, Lilljeborg, Pl. VI, figs. 1—5. Temora velox, Lilljeborg. De Crustaceis ex ordinibus tribus Cladoc. Ostrac. et Copep., p. 177, tab. xix, figs. 9 and 10, and tab. xx, figs. 1—9 (1853). — — Brady. Nat. Hist. Trans, Northumberland and Durham, vol. i, p. 38, pl. i, fig. 16, and pl. iii, figs. 1—11 (1865). Body robust, dorsum strongly arched, head distinct from the thorax, last thoracic segment in the female produced into two strong spines at the ventral angle. Anterior antenne (figs. 1, 2) rather short and stout, not much longer than the cephalothorax, 24- jointed, moderately tapered to the apex, toward which the segments gradually increase in length, those near the base, up to the twelfth, being much broader than long, and those from the sixteenth onward about twice as long as broad; the middle portion of the antenna is densely setose on the outer margin, but the setz are more scattered toward the apex; the right antenna of TEMORA. 57 the male has two long apical joints, at the base of which the hinge is placed, the two joints above and one below being armed with serrated plates ; the 11th, 12th, 13th, and 14th joints have each usually a dis- tinct but short spine, the 15th and 19th bear also similar but larger spines, and the number of joints is reduced to twenty-one owing to the coalescence of some of the number; the middle of the male antenna, as in the previous species, is much swollen. Fifth pair of feet in the female (fig. 3) 4-jointed, the ter- minal joint very small, rounded, and bearing two stout sete, one large and one small, the other joints very much stouter, the penultimate produced below at the inner angle into a long serrated spine; the 2nd and 3rd joints bear each a single small seta. TWifth feet of the male very large and powerful, and pro- vided on their opposing edges with several spines— mostly one in the middle of each joint ; each branch is 3-jointed, the basal joints large and swollen, the ter- minal jomt of one side ending in a blunt doubly toothed broad extremity, that of the other side form- ing along slender claw. ‘The middle segment of the abdomen in the female is much the shortest (fig. 5) ; the last abdominal and the caudal segments are beset with irregularly scattered short hairs or prickles. Caudal segments four times as long as broad; about equal in length to the terminal sete, or to half the leneth of the abdomen. The ova are borne in a large undefined mass on the front of the female abdomen, and large oblong spermatic tubes are often found attached in the same situation in great numbers, 58 BRITISH COPEPODA. depending from the vulva like a bunch of candles. Length ;),th of an inch (1°5 mm.). When alive the animal is of a pale brown colour, but on immersion in Spirit assumes a peculiar vinous red or purple. Temora velow is an inhabitant, almost exclusively, of the brackish water of estuaries and salt marshes, and in such localities I have taken it pretty extensively. I have only once met with it in the sea, amongst Laminarie at Sunderland, and then only one or two specimens were taken. The other localities in which I have found it are, at Hylton on the Wear, Hartle- pool, Alnmouth, Burgh Marsh near Carlisle, Cumbrae, Pensarn (Merionethshire), Oulton Broad and Lake Lothing (Suffolk), Whittlesea Dyke (Cambridgeshire), and in pools near the river Stour at Manningtree. In such situations it often occurs in immense profusion, especially in autumn, when the water has become heated by the direct rays of the sun. Genus 7. Diapromus, Westwood (1836). (Cyclops (in part), Muller. Cyclopsina, Milne Edwards, 1840.) Body elongated, compressed; head distinct from the thorax, anterior antenne 25-jointed, that of the male on the right side hinged. Posterior antenne and organs of mastication as in Calanus. Inner branches of all the swimming feet three-jointed except the first, which has only two joints. Fifth foot consisting of two branches, prehensile in both sexes, the internal DIAPTOMUS. 59 branch much the smaller. Abdomen of the male 5-, of the female 3-joited. Hye situated in the median line. 1. Draptomus Castor, Jurine. Pl. VI, figs. 6—183. Cyclops ceruleus, O. F. Miller. Entomostraca, p. 102, t. xv, figs. 1—9 (1785). — lacinulatus (¢?), Miller. Ibid., p. 105, t. xvi, figs. 4—6 (1785). — rubens (%), Miller. Ibid., p. 104. t. xvi, figs. 1—3 (1785). Monoculus Castor, Jurine. Histoire des Monocles que se trouvent aux Environs de Genéve, p. 50, tabs. 4—6, (1820). Cyclopsina —= M. Edwards. Nat. Hist. Crust., vol. iii, 427 (1840). Diaptomus Castor, Westwood. Partington’s Cyclopedia, art. “ Cyclops ” (1836). — — Baird. Nat. Hist. Brit. Entom., p. 219, tab. xxvi, figs. 1,2,2a—j (1850). — — Claus. Die freil-ebenden Copep., p. 201, t. xxxv, figs. 15 and 16 (1863). — — Lilljeborg. De Crust. ex. ord. trib., t. xii, fig. 10, t. xiii, figs. 1—10, t. xiv, figs. 1—4 (1863). — — Lubbock. Trans. Linn. Soc. Lond., vol. xxiv, p. 197, pl. xxxi, figs. 7—11 (1863). — Westwoodii, Lubbock. Loc. cit., pl. xxxi, figs. 1—6. — Castor, Fric. Die Krustenthiere Bohmens, p. 225, fig. 22 (1871). Anterior antenna (fig. 8) 25-jointed; gradually tapering from the base and beset with setz of mode- rate length, one or two on each segment, except on the terminal one, which has five at its extremity; right antenna of male (fig. 7) provided with a hinge-joint, above which for the length of six segments it is much swollen; the 13th joint is armed with a strong mar- ginal spine, and the 10th and 11th with spines of a similar kind though smaller; the hinge is situated oN 60 BRITISH COPEPODA. between the 18th and 19th joints. The posterior antennee, the mouth-organs, and swimming feet present no marked characters. The fifth pair of feet in the female (figs. 10, 11) are alike on both sides, consisting of a rudimentary one- or two-jointed inner, and a much larger three-jointed outer branch. The inner branch bears three apical spines of variable size, but never very large; the outer branch has the basal joint very large, the second joint small, and the third in the form of a broad sword-like spine attached toward the inner side of the limb ; the second joint bears in addi- tion two small apical spines or setz.; both branches are nearly straight. In the male (fig. 9) the foot of the right side is much larger than that of the left, and terminates in.a long, curved claw ; the inner branch is in both feet quite rudimentary. The last thoracic seoment in the female (fig. 12) is produced downwards at each side into aconspicuous sharply spined process; in the male (fig. 13) it is distinctly angulated, but has no conspicuous spine. The abdomen consists in the female of 3 and in the male of 5 seoments; the caudal segments broad and short; terminal sete strongly plumose, and about half the length of ‘the abdomen. ‘The eye is large and movable, and of a brilhant red. The colour of the animal itself is very variable ; yellowish, red, bluish-green, or brown; once I have seen it so red as to look lke scraps of ani- mated sealing-wax when swimming in the water. In some cases the ovisac is of a different colour from the rest of the animal. Length 39 to ;gth of an inch (1°3 to 2:1 mm.). DIAPTOMUS. 6] Diaptomus Castoris of common occurrence in ponds, lakes, and ditches; its colour and perhaps its varia- tions of structure probably depend much upon the character and quantity of its food as well as upon dis- tinctions of race. ‘The largest specimens are usually found in ditches and rather foul, weedy water; those of mountain tarns and lakes are, as a general rule, considerably smaller, not exceeding ;'sth or 3oth of an inch inlength. The most highly-coloured specimens that 1 have seen were taken in Grisedale T'arn, under Helvellyn, and are referred to above as being of a brilliant vermilion-red. The form described by Sir John Lubbock under the specific name Westwoodw does not appear to me sufficiently well defined or permanent in its characters to warrant its separation as a distinct Species; it 1s indeed, so far as my observation goes, much commoner than the typical D. Castor. The characters upon which Sir J. Lubbock lays most stress are, lst, those of the fifth pair of feet, which do not present any strongly-marked difference except as to the inner branch of that of the female (fig. 11), which is better developed than in the Castor form; 2ndly, in the angulation of the last thoracic segment, which after all appears to me to be nearlyas marked in one form as in the other; 3rdly, in the length and spinous armature of the antennz, both of which are liable to a good deal of variation; but the spine on the antepenultimate joint of the antenna of D. Westwoodw I have found in some cases to coexist with the other distinctive characters of D. Castor. For these reasons I think it best to unite both forms under the old E 62 BRITISH COPEPODA. specific name. The observations made as to the ovisacs and spermatic tubes of Temora velow apply equally to the present species. Genus 8. Istas, Boeck (1864). Body moderately robust, with a well-rounded dor- sum. Abdomen composed in the female of three, in the male of five segments. Anterior antenns 24- jointed, that of the right side in the male forming a geniculated prehensile organ. Posterior antenne as in Calanus. First four pairs of feet with both branches triarticulate. Fifth pair of feet in the female, having the outer branch 3-, the inner 1-jointed ; in the male the outer branch consists of two, the inner of one or two joints. 1. Istas ciavipes, Boeck, Pl. VII, figs. 3—13. Isias clavipes, Boeck. Oversigt Norges Copepoder, p. 18, (1864). Anterior antennz of the female (fig. 4) 25-jointed, about equal in length to the cephalothorax, joints short and broad at the base, and gradually increasing in length to the nineteenth, which is about four times as long as broad; first fifteen jomts of the male antennze each bearing a single club-shaped, ciliated, auditory seta: hinge-joint of the 21-jointed right male as ee ae ISIAS. 63 antenna (fig. 5) situated between the eighteenth and nineteenth joints; eighteenth joimt formed by the coalescence of the normal eighteenth and nineteenth, nineteenth by the twentieth and twenty-first, twentieth by the twenty-second, twenty-third, and twenty-fourth. Mouth organs and swimming feet as in Centropages typicus. Fifth pair of feet, in the female, two-branched (fig. 10), having the outer branch of three broad laminar joints, the second of which is produced at the inner margin into a strong ciliated spine; the third joint is as large as the other two together, is fringed internally with swimming sete and bears at the apex one large and one small spine; inner branch 1-jointed, rudimen- tary, and bears two apical sete. Fifth foot of the _male (fig. 11) also two-branched, that of the right side being the larger; the outer branch in both cases 2- jointed, the second joint large and forming, especially in the right foot, a broadly expanded lamina, bearing three or four small marginal spines, and on the right side a large terminal ciliated spine; inner branch rudimentary; that of the right side provided with swimming sete and 2-jointed. ‘Terminal spines of the swimming feet (fig. 12) elongated, narrow, and bayonet- like, finely pectinated on the inner margin. Abdomen of the female divided into four, of the male into five seg- ments, third segment in the male produced in front into a spiniform papilla. Caudal segments as long as the united length of the last two abdominal segments ; sete equal to half the length of the abdomen. Length -jzth of an inch (1°5 mm.). This fine and very distinct species appears to be 64: BRITISH COPEPODA. generally distributed in the British seas, but nowhere occurs in any great abundance. The localities from which I have specimens are as follows :—Off Robin Hood’s Bay, Yorkshire, dredged in 35 fathoms ; dredged off Portincross, Ayrshire (20 fathoms); off Cumbrae (15 fathoms), i Lough Swilly, Ireland, (8 fathoms) ; taken in the surface-net at Cumbrae, Bridlington Bay, and at Killybegs, Donegal (Mr. H. C. Davison); and amongst fuci in Clifden and Roundstone Bays, Ireland. Genus 9. Cuntropaces, Kroyer (1849). (Ichthyophorba, Lilljeborg. Calanopia, Dana. ? Catopia, Dana.) Body elongated. Head distinct from thorax, more or less distinctly divided by a groove into two seg- ments, and produced into a cloven rostrum. Abdo- men composed of five segments in the male, of three in the female. Anterior antenne 2-4-jointed, that of the right side in the male geniculated and prehensile. Mouth organs as in Calanus, except that the anterior footjaws are armed with strong bristles as in Pontella. Both branches of the first four pairs of feet 3-jointed ; outer branch of the right fifth pair in the male pre- hensile, internal branch adapted for swimming. Hye median and movable. CENTROPAGES, 65 1. Centropacss typicus, Kroyer, Pl. VIII, figs. 1—10. Centropages typicus, Kroyer. Nat. Tidskr. anden. Rekkcs andet Bind, Side 588, (1849). _ — Boeck. Oversigt over de ved Norges Kyster iagttagne Copepoder, p. 19, (1864). Ichthyophorba denticornis, Claus. Die frei-lebenden Copepoden, p. 199, pl. xxxv, figs. 1, 3—9 (1863). —_ os Brady. Nat. Hist. Trans. N. & D., vol.i, . p. 40, pl. iv, figs. 1—6, (1864). Body elongated; last thoracic segment produced downwards at each side (but more strongly in the female than in the male), into a large and strong spine. Anterior antennz as long as the body (fig. 1), bearing a strong pointed tooth on the outer margins of the first, second, and fifth joints; right antenna of the male (fig. 2) hinged between the eighteenth and nineteenth joints, and bearing denticulated plates above and below the hinge, much swollen in the middle, armed with a strong hook-like spine on the margin of the sixteenth joint. Fifth pair of feet in the female (fig. 9) much like the preceding pairs except that the outer branch has the middle joint produced internally into a very long and strong spine; in the male (fig. 10) the inner branch is on both sides adapted for swimming, but the outer branch of the right limb has the last two joints developed into a powerful grasping organ by the conversion of each joint into a curved claw, that of the middle joint being stout, crooked, and denti- culated at the extremity ; the outer branch of the left 66 BRITISH GOPEPODA. foot has only two joints. The terminal spines of the swimming feet are sword-shaped, rather slender, and finely serrated (fig. 7). The first segment of the female — abdomen bears three plumose spines, one of which is stronger than the other two, and the second segment is produced laterally into a papilla for the attachment of spermatophores. Caudal segments short, about as long as the last abdominal segment, setose on the internal margins and bearing five strongly plumose and rather rigid apical sete which are considerably shorter than the abdomen. Length ;'s;th of an inch (1°6 mm.). Colour brown. Except in littoral situations this species seems to be at least as common in the British seas as the following (C. hamatus). It is taken frequently in the North Sea and in the Atlantic by the towing net; indeed few gatherings thus made, if at all good ones, are entirely without it. J have memoranda of its occurrence off the West Coasts of Scotland and Ireland, the Kast of England and Scotland, amongst the Channel Islands, between Gornwall and Cape Clear, &. It occurs, too, amongst dredged material so frequently that it can scarcely in all cases have been captured by the dredge on its way up to the surface. CENTROPAGES. 67 2. Cuntropaces HAMmATUS, Lilljeborg. Plate VIII, figs. 11—13. Ichthyophorba hamata, Lilljjeborg. De crustaceis, &., p. 185, t. xxl, figs. 1—5, 7—9, and t. xxii, figs. 9—12, (1853). — — Brady. Nat. Hist. Trans. N. & D. vol. i, p. 39, pl. iv, figs. 7—10 (1865). “— angustata, Claus. Die frei-lebenden Copepoden, p. 199, t. xxxv, figs. 2, 10—12 (1863). Diaptomus Bateanus, Lubbock. Ann. and Mag. Nat. Hist. (2nd ser.), vol. xx, p. 404, pl. x1, figs. 1—3 (1857). Centropages hamatus, Boeck. Oversigt Copepoder, p. 20 (1864). Body slender, smaller than the foregoing species ; spines of the last thoracic segment also smaller. Anterior antenne destitute of spines, of equal length, but more slender than in C. typicus ; im other respects the same. The fifth pair of feet in both sexes are also similar to the same parts in C. typicus, but much more slender, and the claw of the male right foot (fig. 13) is not denticulated. ‘The spines of the swimming feet differ remarkably from those of C. typicus in having their serrated armature much stronger and the teeth separated one from another by a wide interval (fig. 12). Length ={;th of an inch (1:95 mm ). This species, like the preceding, occurs not uncom- monly at the surface in the open sea and appears to have much the same distribution. I have once taken it between tide marks, amongst Algz in rock-pools near Ryhope (county Durham). 68 BRITISH COPEPODA. Guinus 10. PARAPONTELLA, nov. gen. Head distinct from body. Fourth and fifth thoracic segments united. Abdomen of the male 5-, of the female, 3-jointed. Right anterior antenna of the male provided with a hinge-jomt. Secondary branch of posterior antenne large, 3-jointed. Maxilla minute, consisting of a large basal joint with an elongated terminal palp and two small branchial processes. Mandible slender and twisted, terminal teeth sharp and slender, two of them much longer than the rest (fig. 5); palp consisting of a single 3-jointed branch. Anterior foot-jaw bearing at the apex about six short and strong, curved, plumose spines. Posterior foot- jaw composed of a basal joint of moderate size, and a rudimentary 3-jointed apical portion, the basal joint bearing two large curved plumose sete and two smaller ones. Inner branch of first pair of feet 3-jointed, of second, third and fourth pairs 2-jointed. Fifth pair of feet in the female simple, two-branched; each branch composed of a single joint; in the male, adapted for prehension, and composed of one branch on the left, of two on the right side. The species described by Sir John Lubbock under the name of Pontella brevicorms appears to present some characters distinct enough to require its removal from the genus to which it has hitherto been assigned. The 3-jointed inner branch of the first swimming foot, PARAPONTEILLA. 69 the rudimentary lower foot-jaw and the comparatively poor setose armature of the upper, the single-branched mandibular palp and the peculiar structure of the maxilla are points of difference which seem to me of generic importance. I have had no opportunity of examining living specimens, and cannot in my spirit- Specimens make out eyes of any kind, but I am dis- posed to think that in this matter the species will be found to belong to the subfamily Calanine rather than to Pontelline. 1. PARAPONTELLA BREVICORNIS, Lubbock. Plate IX, figs. 1—16. Ponitella brevicornis, Lubbock. Ann. and Mag. Nat. Hist., 2nd ser., vol. xx, pl. xi, figs. 4—8 (1857). Head separate from the thorax and ending in a short forked rostrum. Superior antenne 18-jointed (fic. 3) about as long as the cephalothorax, mode- rately slender, and (except on the right side in the male) of nearly equal thickness throughout, the first joint large, the next six small, the rest from twice to thrice as long as broad, except the last which is about four times as long as broad and bears a finger-like apical process (longer in the male than in the female) and about seven long apical sete; each joint bears a few short hairs, but the first, eleventh, thirteenth, and sixteenth have each one larger apical seta; the joints of the right male antenne (fig. 2) are greatly reduced in number by coalescence, the last three beimg very long 70 BRITISH COPEPODA. and slender, the limb is much swollen at the hinge, and again a little above, and is provided with denticulated plates above and below the hinge joint; the sete are but few except for a dense tuft at the extremity of the last joint. The rudimentary apical portion of the lower foot jaw (fig. 8) is obscurely (3?) jointed, and on its upper margin bears a corrugated segment sharply separated lengthwise from the lower portion of the limb. Terminal spines of the swimming’ feet, long, slender, and sword-shaped (fig. 13) ; the secon- dary spine is much larger than usual, and both are finely serrated on the inner edge. Fifth pair of feet in the female (fig. 12) two branched ; branches nearly straight, cylindrical, and one-jointed; the inner one short and cloven at the apex, the outer twice as long, bearing one short spine at the middle of the outer margin, and one very long and two short at the distal extremity. Fifth pair in the male (fig. 11) composed of one branch on the left and two on the right side, three-jointed ; those of the left foot broad and sub- quadrate, the last jomt spinous at the angles; first joint of the right foot narrow, and having a short one- jointed branch which ends in a curved claw; second joint short and armed with a curved spine on the inner margin; third jot produced into a long slender claw. Abdomen of the female (figs. 15, 16) three- jointed ; the first segment short and stout, the second smaller and produced downwards as far as the middle of the dorsal surface of the third segment; produced also into two small lateral spines. Caudal segments as long as the last abdominal segment in the female, PONTELLINA. v1 in the male as long as the last two. The third and fourth abdominal segments in the male each bear a sharp projecting spine on the right side, and the last thoracic segment is produced downwards into a hook- hike spine. The caudal setz are not as long as the abdomen. Length of the animal ;/;th of an inch (1-5 mm.). Colour dark brown. This species is at times taken in great abundance by the surface net. J have a gathering taken in this way by Mr. H. C. Davison off the Yorkshire coast, which more than filled a four ounce bottle, and con- sisted of about equal quantities of P. brevicornis, Ano- malocera Patersonw, and larval decapods. I have also notes of its occurrence in surface gatherings from Bridlington Bay, the Channel Islands, Westport Bay (Ireland), and Kinsale Harbour; in gatherings made amongst Alezw and Zostera at Clifden Bay and the Scilly Islands, as well as in tide pools on the Durham coast; also in dredged material from Cumbrae and Portincross, Firth of Clyde. Sub-famiy 2.—Pontstiina, Dana. Having two or more paired lateral eyes, in addition to a large median eye which usually springs from behind the rostrum as a projecting globe; in other respects like Calanine. aa BRITISH COPEPODA. Genus 11. Pontenua, Dana (1849). (Pontia, Milne-Edwards.) Head distinct from thorax; fourth and fifth tho- racic segments coalescent. Abdomen of the male 5-, of the female (2-?) or 3-jointed. Anterior antennz — 23- or 24-jomted; the sixth and seventh joints coalescent or distinct; the right antenna of the male greatly swollen in the middle from the thirteenth to the sixteenth, and hinged between the nineteenth and twentieth joints; the seventeenth, eighteenth, and nine- teenth united into one long joint, which is toothed on the inner margin; the twentieth and twenty-first joints also coalescent and toothed. Posterior antenna having a well-developed secondary branch. - Maxilla (Pl. 10a, fig. 6), well developed, composed of a broad prehensile portion, witha large 3- or 4-lobed branchial palp. Mandible-palp 2-branched, of mode- rate size. Basal portion of the posterior foot-jaw produced into three setiferous digits, apical portion 4-jointed, elongated. Inner branches of all the swimming feet 2-jomted. Fifth pair of feet on the right side only in the male, forming a powerful clasp- ing organ, that of the left side much less strongly developed. PONTELLA. Ea 1. Ponretta Wottastont, Lubbock. Pl. X a, figs. 1—12. Pontella Wollastoni, Lubbock. Ann. and Mag. Nat. Hist. series 2. vol. xx, p. 406, pl. xi, figs, 9—11, 18, and pl. x, fig. 15, (1857). — helgolandica, Claus. Die frei-lebenden Copepoden p. 208, taf. ii, figs. 5—7; taf. xxxvi, figs. 1—10; taf. xxxvii, fig. 7, (1863). Body elongated ; anterior antennz about as long as the cephalothorax, that of the male, on the right side, haying two hook-like spines, one on the sixteenth and one on the seventeenth joint (fig. 2). The inner branch of the mandible palp is 4-, the outer 2-jointed. The right foot of the fifth pair in the male is 4- jointed (fig. 10); the second joint very broad, and produced at the inner margin into a long hook-like spine, the third joint slender, forming a movable prehensile hand, to which is attached the fourth joint in the shape of a strong claw; the foot of the left side (fig. 9) consists of a broad 2-jointed basal portion, to the extremity of which are attached two short branches, one subtriangular, which terminates in two small claw-like processes, the other broad, 2-jointed, the terminal joint bearing three mar- ginal sete, anda fringe of short fine hairs. The rostrum is broad and strong. Lateral angles of the last thoracic segment equal and armed with short hooks. Abdomen slender; the last two segments, in the male, short; caudal segments elongated, in the 74 BRITISH COPEPODA. male, as long as the last three segments. Abdomen of the female 3-jointed, both lenses of the paired eyes, and that of the median eye, smaller than in the male ; the fifth foot (fig. 11) is composed of a 2-jointed basal portion, to which are attached two long sub- triangular plates. Length $th of an inch (8 mm.). This species is known to me only from the type specimens which were taken by Sir John Lubbock at Weymouth, and which by his kindness I have had the opportunity of examining. They are not now ina — condition to allow of accurate description, and I am, therefore, indebted chiefly to the excellent figures and descriptions of Dr. Claus and Sir John Lubbock, for the account of the species here given. That the Pontella helgolandica of Dr. Claus is identical with Sir John Lubbock’s P. Wollastoni, there can be no doubt. Genus 12. ANomanocera, Templeton (1837). (Ireneus, Goodsir.) Body elongated. Head produced into a strong furcate rostrum, distinct from the thorax and incom- pletely divided by a transverse groove into two seg- ments. The median eye is stalked. Lateral eyes sessile, each composed of two lenses (fig. 14). Notopterophorus. each of thoracic | like seg- | expan- ie ments | sions DW JOU eo are a caccacheuvesacreacaete nea sacee (orem Ascidicola, Sub-family 1. NortoDELPHYINA. Body flattened, head consolidated with the first thoracic segment; six abdominal segments in both sexes. Anterior antennz 10—15-jointed, and in the male adapted for clasping, as in Cyclops. Caudal NOTODELPHYS. 125 seeoments bearing numerous long, finely plumose sete. This sub-family contains only one genus—Noto- delphys. Genus 1. NotoprtpHys, Allman (1847). Body elongated, cephalothorax somewhat depressed, abdomen much attenuated, cylindrical; caudal appen- dages consisting of four large plumose sete attached to the apex of each segment, together with two or three small lateral setz. Anterior antenne com- posed in the male of 10 or 11, in the female of 15 joimts ; posterior unbranched, armed at the apex with a strong movable claw and several curved sete. Mandible-palp 2-branched; basal portion very large and broad, internal branch composed of two, external of two or more joints. Maxille composed of a prehensile or biting segment, which is provided with strong curved sete, and three or four broad laminz fringed with plumose branchial filaments. Anterior foot-jaws stout, subtriangular, 5-jointed, the basal joint constituting the bulk of the lmb; posterior slender, 3-jointed; both pairs armed with numerous strong curved sete on the inner margin. Branches of the first four pairs of feet 3-jomted and beset with finely plumose sete ; fifth pair very small, 2-branched, branches composed of one joint only. 126 BRITISH GOPEPODA. 1. Noropenppys Auumant, Thorell. Pl. XXV, figs. 1—10. P Notodelphys ascidicola, Allman. Ann. and Mag. Nat. Hist. vol. xx, pl. 1, figs. 1—13 (1847). — — Baird. Brit. Entom., p. 238, pl. xxx, figs. 7, 8 (1850). — Allmani, Thorell. Bidrag till Kannedomen om Krustaceer som lefva i arter af Slagtet Ascidia, p. 31, tabs. i and ii, fig. 1 (1859). P — elegans, Thorell. Loc. cit., p. 39, tab. iv, fig. 5. P —~ rufescens, Thorell. Ibid., p. 35, tab. ui, fig 2. Anterior antenne (fig. 2) shorter than the first body-segment, stout at the base and gradually taper- ing to the apex, densely beset along its whole length with finely plumose hairs; the second joint is very short, the first, third, fourth, and fifth large, the fourth and fifth nearly equal, and twice as long as any of the remaining joints, which are short and of nearly equal length. Posterior antenne (fig. 3) robust, the third and most slender joint being scarcely more than twice as long as broad. Mandible palp (fig. 4) stout, the outer branch 3-jointed.* The maxilla (fig. 5) consists of a strongly clawed or setose prehensile portion, with a branchial palp, which is composed of two large and two small laminz, bearing marginal plumose filaments. The anterior foot-jaws (fig. 6) are very stout, bearing several short digitiform * This is misrepresented in the plate, the portion shown as a long terminal joint being in reality the thickened base of the large apical seta. NOTODELPHYS. 127 marginal segments, all of which have stout apical setz, the stronger ones being plumose or pecti- nated, last three joints very small; posterior foot- jaws (fig. 7) slender, 38-jointed, with several plu- mose marginal sete, that arising from the second joint being much the strongest ; the terminal joint is very small, the penultimate much larger, and the first three or four times as large as the second. The first pair of swimming feet (fig. 8) has the external margin of the first jomt of the outer branch fringed with short strong hairs (‘‘dentibus angustis, dense serratus,’ Thorell); the margins of the two following joints, as well as those of the inner branch, are perfectly smooth ; in the following pairs of feet, how- ever (fic. 9), all the joints of the inner, as well as the © first of the outer branch, are finely fringed on their external borders ; all the sete are very finely plumose (much more finely than could be shown in the eneraving). The fifth pair of feet (fig. 10) are com- posed each of two 1-jointed branches, the outermost of which is of oblong subquadrangular outline, and bears a long spine at the apex, and a short tooth-like process on the inner margin; the inner branch is broader and shorter, and has two apical seta, the innermost of which is stout and spine-like; there are also four small teeth on the inner margin; the peduncle of the foot is armed at its inner angle with a row of about six small spines. Caudal segments about once and a half as long as the preceding abdominal ring; the small lateral setz situated a little below the middle of the external margin; internal 128 BRITISH COPEPODA. margin of the segments finely ciliated. The ovarian sac forms a conspicuous prominence on the back of the animal, and has its angles well rounded. The ovaria, according to Thorell, are greenish yellow, the ova brown green. Length* of female $th—+th of an inch, of male ;,th—~;th of an inch (3—5 and 13—2 mm.). Mr. Norman has recorded this species as occurring in the “ branchial sac and water-passages of Ascidia venosa”’ from Shetland. I have not myself seen any British specimens, and my drawings have been made entirely from Swedish specimens, for which I am indebted to the kindness of M. Thorell. The follow- ing list of localities is given by Dr. Baird (loc. cit.), but it must be remembered that at the date of his work the Ascidian parasites were scarcely at all known, and it is extremely probable that many of the specimens then named N. ascidicola might now be referred to other species of the genus. ‘‘ Belfast Bay; Strang- ford Lough, County Down; W. Thompson and G. C. Hyndman, Hsqrs., Killery Bay, County Galway; R. Ball and W. Thompson, Hsqrs., Bangor, County Down; R. Peterson, Esq., Glandore Harbour, County Cork, Dublin Bay, and Southampton Water; George J. Allman, Esq. In the branchial sac of the Ascidia communis.” The characters upon which M. Thorell has founded the seven species of Notodelphys described in his work are mainly the length and proportions of the * The lengths of the species of Notodelphys, except N. prasina, are those given by M. Thorell. NOTODELPHYS. 129 caudal seoments and the position of the lateral sete upon their external margins, together with the appearance of the external margin of the first joint of the outer branch of the first foot. The marginal spines of this branch, the setose armature of the second antenne, and of the fifth pair of feet, &Xc., afford other means of specific diagnosis; but it seems to me that the distinctions are, in some cases, at any rate, much too trivial, and that in all probability a more extended investigation would lead to the conclu- sion that at best some of these forms deserve to be classed only as varieties. In the case of the present species the distinctions drawn between it, NV. rufescens, and N. elegans, do not appear to be of specific import- ance. | As regards Mr. Allman’s description and figures of Notodelphys ascidicola, 1t must, I fear, remain doubtful to which species of the genus they were meant to refer; it 1s, indeed, more than probable—from the number of localities given in Mr. Allman’s paper that several species of Notodelphys were the subjects of description, while some of the figures (14, 15, and 21) undoubtedly refer to a quite distinct genus—Ascidicola, Thorell. It seems best, therefore, to follow M. Thorell, discarding altogether the specific name Ascidicola, which, however, will stand as the designation of a separate genus. 136 BRITISH COPEPODA. 2. NoroprenpHys cERuULmA, Thorell. Pl. XXVII, figs. 10—13. Notodelphys cerulea, Thorell. Loe. cit., p. 37, tabs. iii and iv, fig. 4 (1859). P tenera, Thorell.. Ibid., p. 36, tab. iii, fig. 3. This species differs scarcely at all from the prece- ding. The posterior antenne (fig. 11) have near the margin of the apical joint two subcrescentiform rows of small cilia, the branches of the fifth pair of feet (fig. 13) are somewhat shorter and wider than in N. ascidicola, and the first foot has the outer margin of its first joint (fig. 12) either smooth or very finely denticulated. The ova and ovaria are said to be blue. Length of female $th— th of an inch (8--45 mm.), of male ;',th—;;th of an inch (1}—1$ mm.). I cannot find any good reason for separating this from the foregoing species, but for the present retain it, giving drawings of the more prominent distinctive characters. I have notes of its occurrence in the following British localities:—In Ascidia parallelogramma, off Hawthorn (Durham Coast); in Ascidia parallelo- gramma and A. venosa, Shetland, and from between tide-marks, Roundstone (fev. A. M. Norman). 3. NotopeLpHys aGiLis, Thorell. Pl. XXVI, ‘igs. 1—10. Notodelphys agilis, Thorell. Loc. cit., p. 40, tabs. iv, v, fig. 6 (1859). The caudal sezments of the abdomen are here more NOTODELPHYS. Bot than twice as long as the preceding segment, and the lateral seta 1s placed on the middle of the external margin (fig. 9). Both branches of the fifth pair of feet (fig. 10) are very much smaller than in either of the foregoing species and much more slenderly spined. Length of female ;yth—{th of an inch (2—3 mm.), of male ;/;th of an inch (3 mm.). N. agilis has occurred in Ascidians taken off the coasts of Durham and Yorkshire, in depths of from twenty to thirty fathoms, and among specimens from the branchial sac of Ascidia sordida, Shetland, sent to me by the Rev. A. M. Norman. 4. NotopetpHys prRasINA, Thorell. Pl. XXX, figs. 11—15. Notodelphys prasnia, Thorell. Loc. cit., p. 41, tab. v, fig. 7 (1859), The caudal segments (fig. 15) are in this species much shorter and stouter than in any other, their length being not more than equal to the breadth. The two principal tail sete, more especially the inner one, are very broad. The branches of the fifth pair of feet (fig. 14) are very small, the outer about thrice as long as broad, the inner about as broad as long. Length of female ;;th of an inch (2°3 mm.). This species was more abundant than any other in -a collection of Hntomostraca taken from the branchial sacs of Ascidia mentula at Oban by the Rev. A. M. Norman, to whom I am much indebted for the is} BRITISH COPEPODA. opportunity of examining his captures. Mr. Norman has also recorded N. prasina as occurring in the same Ascidian in Shetland. Sub-family 2. Doropycina, nov. sub.-fam. Body more or less compressed; anterior antennz short, 8—10-jointed; in the male not modified for clasping. Caudal segments curved and bearing very small apical spines. Genus 2. Doropyeus, Thorell (1859). Body dorsally elevated, somewhat compressed ; caudal segments bearing at their apices curved spines or hairs. Anterior antennz 8- to 10-jointed; very small, about one third the length of the first body segment, posterior 38-jointed, terminating in a curved claw. Basal jomt of the mandible-palp large, 2-branched, the external branch composed of one, the internal of two joints. Maxille composed of a prehensile aculeated portion, and three or four more or less rounded segments, which are fringed with finely plumose branchial filaments. First pair of foot- jaws broad, subtriangular, 5-jointed, the last joint minute; second pair elongated, 3-jointed; both pro- vided with numerous strong marginal sete. Branches of the first four pairs of feet usually 3- (rarely 2-) DOROPYGUS. ba jointed, setee naked or finely plumose ; fifth pair small, 1-jointed. Inhabiting the branchial sac of various simple Ascidians. 1, Dororveus runex, Thorell, Pl. XXVIII, figs. 1—12. Doropygus pulex, Thorell. Loc. cit., p. 46, tab. vi, fig. 8 (1859.) Adult female.—Cephalothorax produced into a short, blunt, triangular rostrum, third and fourth thoracic segments united to form the ovarian envelope. Abdomen much narrower than the cephalothorax (fig. 1), and bent upon it so as to form almost a right angle. Fifth abdominal segment longer than the fourth (figs. 11, 12), partially furcate, and divided into two subtriangular sezments. Caudal segments very long and slender, transversely divided near the middle, curved and divergent, and bearing three or four minute apical sete. Anterior antenne 10- jointed, the two basal joints about once and a half the width of the third joint, the third, fourth, fifth, and sixth progressively decreasing in width, the last four subequal as to width, the sixth jomt longer than any except the first. The whole limb is densely beset with long hairs on the external margin and apex, and the second joimt has also two conspicuous tooth- like spines. The posterior antenna (in the adult) has the claw longer than the second joint (fig. 5, Pl. XXVIII, is taken from an immature specimen, and 134 BRITISH COPEPODA. does not show correctly the relative lengths of the joints in the adult). The first pair of feet (fig. 8) have both branches broad, 3-jointed, and of nearly equal length, all the jomts short and broad, the terminal ones broadly rounded or subtruncate at the apex; marginal sete long, stout, and densely plumose; spines of the external branch long and stout. The second, third, and fourth pairs (fig. 9) are longer than the first, the spines of the external branch are smaller, the setze also much smaller and destitute of plumes. The fifth pair consist each of a single small bisetose lamina. The caudal segments are about as long as the preceding four abdominal rings, slender, curvate, and jointed near the middle, the apices bearing three minute hairs (figs. 11, 12).* Length 5th of an inch (2°1 mm.). Many immature specimens of this species were found in Ascidians dredged by Mr. Robertson, the Rev. A. M. Norman, and myself, off the coasts of Durham and Yorkshire, and also by Mr. Norman at Oban and Shetland. Except a few kindly sent to me by M. Thorell, I have seen no adult of D. pulex. On this account, probably, my drawings do not in all respects agree with those of M. Thorell. The British species of the genus, and, indeed, all the Ascidian parasites of Britain require much closer and more * The figures of anterior antenne and caudal segments given in Pl. XXXI, figs. 1 and 2, represent either an unnamed species or a variety of D. pulex; at present I prefer to adopt the latter supposition, as the general characters of the specimens coincide with those of D. pulex. The specimens were found by Mr. Norman in Aseidians from Roundstone Bay, Ireland. DOROPYGUS. ae extended investigation than I have had the oppor- tnnity of bestowing upon them. I believe, however, that the representations given in these plates, though unavoidably incomplete, will be found to be correct as far as they go. 2. Dororyeus auritus, Thorell. Pl. XXIX, figs. 1—11; Doropygus auritus, Thorell. Om Krustaceeri Ascidier, &c., p. 50, tabs. vu and viii, fig. 10 (1859). Adult female.—Thoracic segments separated at their junctions by deep sulci, and produced into gibbous prominences; head as seen from the side subtriangular ; caudal seoments (fig. 11) stout and slightly curved, and armed at the apices with four or five curved hook-like spines. Anterior antennz (Pl XXIX, fig 2) having the first two joints greatly dilated, and bearing several stout sete, but no spines, 8-jomted. The swimming feet do not differ materially from those of D. pulex, except that the inner branch of the first pair (fig. 8) is only 2-jointed, and the setz of all are distinctly plumose. The second joint of all—more especially of the outer—branches is much shorter than the first and third. Fifth pair of feet (fig 10) small, oblong- ovate, bearing a few irregularly placed, minute, marginal cilia, the basal portion having also a small setiferous tubercle or rudimentary external branch. 136 BRITISH COPEPODA. Length of female sth—th of an inch (31—5 mm.), of male 3'5th of an inch (1 mm.). Mr. Norman records this species as having been taken from “the branchial sac and water-passages of Ascidia mentula,” in Shetland. I have myself seen no specimens except Swedish ones sent by M. Thorell, from which my figures were drawn. 3. Doropyeus Normani, nov. sp. Pl. XXXII, figs. 1—14. Adult female.—Cephalothorax subpyramidal, attenu- ated towards the front, ovarium broadly rounded behind. Anterior antenne (fig. 2) 10-jointed, the two basal joints very broad, the second short and bearing two stout spines on the outer margin, the remaining eight joints successively narrower to the apex and subequal, the fourth and seventh, however, being longer than the rest; the whole limb dorsally beset on its outer margin with long sete, which are either very indistinctly, or not at all, plumose. Apical claw of the posterior antenna (fig. 3) very much shorter than the second joint. The mandible-palp (fig. 4) has the outer branch (a) slender, indistinctly biarticulate, and provided with five setz, the inner branch (0) 3-jointed, its last jomt bearing a series of minute spine-like cilia on the outer margin. The ‘“ external lamina”’ of the maxilla (fig. 5, / e) bears four sete, the ‘‘ ultimate lamina’”’ (/ w) seven, and the ‘‘ middle DOROPYQUS. Lo7 lamina” (/ m) four sete, all of them being, as usual, finely and densely plumose, and doubtless branchial in function. The first foot-jaw (fig. 6) does not differ materially from that of D. pulex; the second (fig. 7) is small, subovate, and fringed with about ten plumose hairs. Branches of the first pair of feet (fig. 8) nearly equal; marginal spines of the external branch long and slender; branches of the second and third pairs (fig. 9) subequal, the external branch bearing setee in place of spines, the internal branch 2-jointed ; fourth pair (fig. 10) more slender and sparingly seti- ferous, the joints of the outer branch dilated and obliquely produced at the distal extremity, and narrowed at the base; fifth pair (fig. 11) three or four times notched towards the extremity of the inner edge, and bearing two short terminal setz; penulti- mate abdominal somite rather shorter than the last, which is partially divided so as to form two sub- triangular segments (fig. 15). Caudal rami (fig. 10) distant, nearly straight, about once and a half as long as the last abdominal segment, bearing two very minute apical hooks (fig. 14). Length nearly $th of an inch (3°3 mm.). This species is undoubtedly very nearly allied to, if not identical with D. psyllus, Thorell, but the maxillee and foot-jaws differ decidedly from those of that species as described in M. Thorell’s work. The replacing of the spines of the third and fourth feet by long sete, and the dentated margin of the last joint of the inner branch of the mandible palp are dis- tinctive characters, as also is the serrated outline of 138 BRITISH COPEPODA. the spines of the first feet* (fig. 12). Whether these distinctions will be found on further research to hold constantly good, one may perhaps doubt, but for the present there seems no sufficient reason for withholding from this form a specific name. But the inconstancy of characters amongst the Notodelphyide is extremely bewildering, and until much more attention has been paid to them it 1s impossible to define with accuracy the limits of species. In this particular instance the difficulty is the greater owing to M. Thorell’s imperfect account of his Doropygus psyllus, of which he had found only two specimens, a number which is often insufficient for the purpose of complete description. Doropygus Normani occurred in some abundance in a collection of parasites found in the cavities of Ascidians which were taken between tide-marks at Roundstone, Ireland, by the Rev. Alfred Merle Norman, whose name I am glad to have the oppor- tunity of associating with the species. 4. Doropyeus Porcicaupa, nov. sp. Pl. XXVII, figs. 1—9 ; and Pl. XXXIITI, 14—16. Adult female.—Basal joint of the anterior antenna * The substitution of sete for spines on the margins of the external branches of the swimming feet is an important feature, if constant, but in some examples one or more of the set2 were wanting, and there seemed to be small spines closely adpressed to the limb; I could not, however, satisfy myself whether or no these might be the scars or broken extremities of lost sete. DOROPYGUS. 139 very large, bearing several long, stout, and often densely plumose sete (fig. 2), and two slightly curved spines; second, third, fourth, and fifth joints succes- sive more slender, sixth and seventh of about equal width, last three much smaller; the whole limb is beset with stout sete which, except on the basal joint, are only slightly or not at all plumose. Terminal claw of the posterior antenna (fig. 3) much shorter than the second joint. Both branches of the first pair of feet (fig. 5) 3-jointed, their sete, like those of the other feet, finely plumose ; marginal spines entire at the edges. The articulations of the outer branches of the second, third, and fourth pairs of feet (figs. 6, 7) are very oblique, each segment being contracted at base and dilated at apex, as m D. Norman; the maxille agree in every respect with D. Norman, but the second pair of foot-jaws (Pl. XXXITT, fig. 15) are hike those of D. pulex, to which species also the caudal seoments closely approximate in character. The Species seems in fact to occupy an intermediate position between D. pulexand D. Norman. Fifth foot simple, bearing two short setze at the apex, which is obliquely truncate (fig. 8), inner margin ciliated. Last abdominal segment (fig. 9) partially divided so as to form two subtriangular portions; caudal see- ments elongated, much longer than the united lengths of the two preceding, convoluted at the apex, and bearing three minute terminal hairs. Length 7th of an inch (4 mm.). 140 BRITISH COPEPODA. Doropygus porcicauda was found very commonly in Ascidians dredged by the Rev. A. M. Norman in Birtirbuy Bay, Ireland; also in specimens of Ascidia parallelogramma dredged in a depth of twenty-seven fathoms off Hawthorn on the Durham Coast. Genus 3. Botacuus, Thorell (1859). Body elongated, narrow, fusiform; caudal rami armed at the apex with curved spines. First pair of antenne 8-jointed (9-jomted, Thorell); second pair 3-jointed, clawed at the apex. Mandible-palp 2- branched, the inner branch 2-, the outer 1-jointed. Maxille composed of a basal masticatory portion and a trilaminar setiferous palp; first pair of foot-jaws stout, subtriangular, 5-jointed; second pair slender, setiferous at the apex. First four pairs of feet with both branches 3-jointed, jomts of the inner branch hispid at the margins; fifth pair rudimentary, 1- jointed. 1. Boracuus cytinpratus, Thorell. Pl. XXXITT, figs. 1—13. Botachus eylindratus, Thorell. Om Krustaceer i Ascidier, p. 55, tab. ix, fig. 12 (1859.) Female.—Animal elongated, curvate (figs. 1, 2), abdomen slightly more slender than the thorax; NOTOPTEROPHORUS. 14] caudal rami abruptly flexed upon the abdomen, bear- ing two strong curved spines and a few sete (fig. 13). Anterior antenne short, bent at a right angle in the middle (fie. 3); distal half densely setiferous ; poste rior antenne (fig. 4) stout. The inner branches of the swimming feet are short (figs. 10, 11) and destitute of marginal spines, but bear three or four slender terminal setz; the marginal spines of the outer branches (fig. 11, a) are surrounded with a delicate ciliated lamina. Fifth pair (fig. 12) 1-jointed, with three apical cilia, two long and one short. Length ;*sth of an inch (1'4 mm.). In the branchial sac and water-passages of Ascidia mentula, Shetland and Oban (Rev. A. M. Norman). Genus 4. NotopreropHorvs, Costa ($852). BAY Body composed of ten segments and provided with several dorsal wing-like expansions ; anterior antennz 10- (8-, Hesse) jointed ; posterior 3-jointed, clawed at the apex. Mandibles, maxille, and foot-jaws, similar to those of Doropygus. Inner branch of first pair of feet 2-jointed; the rest have both branches 3-jointed. Except for the peculiar wing-like dorsal appendages there seems to be little to separate this genus from Doropygus. Perhaps, indeed, we may look upon these expansions as only an extreme development, with modification, of the dorsal gibbosities of UD. auritus. 142 BRITISH COPEPODA. ]. NoropreropHorvus papiLio, Hesse. Pl. XXXI, figs. 3—12. Notopterophorus papilio, Hesse. Annales des Sciences Naturelles (1864), sér. 5, Zool., tome i, p. 338, pl. xi, figs. 1—13; vol. in, p. 221 (1865). The animal is composed of a slender body, on the dorsal aspect of which the delicate membranous integument is produced into six (Hesse) large bifur- cated wing-like expansions (figs. 3, 4). The antennz are very like those of Doropygus ; the anterior (fig. 5) are 10-jointed, the first two joints being very large, the rest very much narrower and shorter, and tapering gradually to the apex; the posterior are 3-jointed (fig. 6), the joimts successively decreasing in size from the first; terminal claw small. Mandible well developed (fig. 7); basal joint of the palp large, secondary branch small, 1-jomted. Inner branch of the first pair of feet (fig. 11) 2-jointed, shorter than the outer branch; the first joint short ; second joint of the outer branch very short. Fifth pair appa- rently absent. Caudal segments of moderate length, cylindrical, tapermg, and armed at the apices with four small hook-hke spines (fig. 12). ‘* Colour of the head white, of the occiput, the first two abdominal seoments, and the eye purplish-red; the rest of the abdomen yellow, and the intestinal tube black, thorax apple-green ; feet and membranous expansions white.” Length $th of an inch (5 mm.). NOTOPTEROPHORUS. 143 Found by the late Mr. Albany Hancock in the branchial sac and water-passages of Ascidia mentula from Shetland, and more recently by the Rev. A. M. Norman in Ascidians from Oban, Loch Fyne, and Herm (Channel Islands). My knowledge of this species is derived entirely from M. Hesse’s memoir, and from specimens kindly given and lent to me by my friend the Rev. A. M. Norman; but owing to the long immersion of the animals in spirit I have not been able to observe satisfactorily many of their characters, especially those of the delicate membranous wing-like expan- sions, which, when exposed to the action of alcohol, become shrivelled, opaque, and shapeless. I therefore give a short abstract of M. Hesse’s description :— These expansions, which are six in number, are mem. branous, flat, papillose, hyaline, contractile, and fixed by the base to different parts of the body. The first is triangular, divided at the extremity into long lashes, and fixed to the back of the neck, forming a sort of hood for the protection of the head; the other four expansions are lateral, placed two at the base of the neck, the other two at the middle of the second thoracic segment ; they, especially the second pair, are much larger than the first, and are also divided into lash-like extremities. These appendages, closely resembling in general effect the wings of a butterfly, are, of course, not used in the same way, but are nevertheless moved with considerable energy by means of the powerful muscles to which they are attached, and they are endowed at all points with a 144, BRITISH COPEPODA. contractility which modifies their form according to the will of the animal. The use of these expansions is unknown, but may probably, M. Hesse thinks, be to act as points dappw for the movements of the creature, or to aid in removing obstacles from its path. For my own part I find it difficult to believe that these excessively delicate organs can be of much use for such purposes, or to understand why, if they are so used, they should be entirely wanting in so many other species which live under the same condi- tions. We must, I think, admit that their use is at present quite unknown. | NoToPTEROPHORUS ELONGATUS, Buchholz. Beitrige zur Kenntniss der Innerhalb des Ascidien lebenden parasitischen Crustaceen des Mittelmeeres, ee 127, taf. vin, fig. 6, and taf. ix, fig. 6. One or two specimens, which, I have no doubt, were referable to this species, occurred amongst those sent to me by my friend the Rev. A. M. Norman, but they seem to have been lost during examination, and I am now, unfortunately, unable to figure or describe them. | Sub-family 3. Ascipicotinm, Nov. sub-fam. First and second thoracic segments coalescent ; abdomen composed in the female of five, in the male of six segments. Matrical envelope formed by a ASCIDICOLA. 145 division of the covering of the fifth somite into two laminar folds. Genus 5. ASCIDIOOLA, Thorell (1859). (Coiliaca, Hesse.) Body elongated, narrow, subcylindrical; abdomen a little narrower than the cephalothorax; caudal rami short, armed with several setz. Anterior antennz 7-jointed (5- or 6-jointed, Thorell), short and stout ; posterior 8-jointed, clawed. Hxtremity of the man- dible divided into several sharp, slender teeth; palp simple, 2-jointed. Maxillz composed of two seti- ferous laminz. First pair of, foot-jaws short and broad, 2-joimted; second pair small 1-jointed, seti- ferous. Four pairs of very small feet, branches 2-jointed ; fifth pair wanting. Two ovaries. Ovisacs composed of two delicate leaf-like lamine. 1. Ascipicota RosEA, Thorell. Pl. XXX, figs. 1—10. Ascidicola rosea, Thorell. Om Krustaceeri Ascidier, p. 59, tabs. ix and x, fig. 13 (1859). Notodelphys ascidicola (jun.), Allman. Ann.and Mag. Nat. Hist., vol; xx, pl. 1, fig. 14, and pl. ii, figs. 15 and 21 (1847). Female.—Anterior antenne (fig. 2) extremely short, stout, 7-jointed, beset with numerous short setzx; terminal joint of posterior antenne long and narrow, bearing two apical claws (fig. 3). | Mandible-palp 146 BRITISH COPEPODA. (fig. 4) armed with six stout spine-like seta, two of which are much longer than the rest. Lobes of the maxille (fig. 6) broad, and armed at the apices with several stout sete; first pair of foot-jaws (fig. 7) very broad, shortly aculeate at the apex; second pair (fig. 8) much smaller and more slender, 1-jointed, bearing four slender terminal setz. Outer branches of the swimming feet bearing on the basal joint one short apical spine, and on the second joint four or five somewhat longer spine-like sete. The basal joint of the inner branch in the first pair (fig. 9) is destitute of sete, but the second joint bears four short spines, and one excessively long seta; the basal joint in the second, third, and fourth pairs has a single apical seta of moderate length, while the second joint bears three very long setz. The penultimate segment of the abdomen bears at the posterior angles a brush of minute hairs. Length 1-5th of an inch (5 mm.). This species occurred not uncommonly in specimens of Ascidia mentula dredged by the Rey. A. M. Norman at Oban and in Birtirbuy Bay, and in Ascidia sordida at Shetland; my own collection contains several specimens taken from Ascidians which were dredged off the Durham Coast. Family 5. Buproripa, Thorell. Body not distinctly segmented, anterior antennz small and rudimentary, two- or three-jointed, poste- rior one- or two-jointed. Mandibles destitute of palps. ASCIDICOLA. 147 Maxille and foot-jaws small, short and broad, adapted for grasping. Feet small, first four pairs two-branched. No external ovisac. Abdomen very small. Genus 1. Enterocona, Van Beneden (1861). Head distinct from thorax; anterior antenne simple, two-jointed, posterior one (?)-jointed. Mouth-organs minute, rudimentary. Posterior foot-jaws larger, 2- jointed and having a rudimentary palp. Four pairs of feet, short, two branched, much like the antennze in general appearance ; abdomen rudimentary, bifid. The mouth-organs, especially, of this genus seem to require more minute examination. The animal is of a sedentary and degraded type, very like in general ap- pearance, as M. van Beneden remarks, to some of the Tardigrada. Ihave not myself seen any perfect speci- mens, and though, in deference to Dr. Claus’ opinion, associating it with Buprorus, | must confess some doubt as to whether this may ultimately be found to be its proper position. M. van Beneden has not given any precise definition of the genus, but the foregoing is condensed so as to embody what appear to me the most important points of his description. 1. Enterocoua eruca, Norman. Enterocola eruca, Norman. Last Shetland Dredging Report, p. 300 (1868). “ Alhed to Hnterocola fulgens, Van Beneden (‘ Re- 148 BRITISH COPEPODA. cherches sur la Faune littorale de Belgique, Crus- tacés’ (1861), p. 149, pl. 26), but is apparently distinct. The feet have one branch, stout, papillary, not furnished with any claw, the other much more slender, terminating in three minute curved spines. The fifth segment of the body has a cylindrical tuber- cular process on each side of the back. The abdomen is composed of two (? three) articulations, and ter- minates in a furea, the branches of which are shorter than broad and are furnished with a spine at the tip. Adhering to the intestine of Ascidia intestinalis.” Mr. Norman’s single specimen of this animal, though kindly placed at my disposal, 1s not in a condition to allow of any satisfactory dissection, owing to the unfortunate drying up of the preservative spirit. I am unable, therefore, to add anything to the description quoted above, which doubtless embodies all that could be made out by examination of the animal in its entire condition. Fig. © ON OD Oo BH CG DO PLATE I. Calanus finmarchicus. . Rostrum. . Anterior antenna of female. . Posterior antenna. . Mandible and palp. . Maxilla, (6) branchial plates. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of fifth pair. . Abdomen of female. 10. 1%. 12. Terminal spine of swimming foot. Right fifth foot of male. Terminal joints of anterior antenna of male. KCo.imp. Je =r WV SV ES TC Fig. O ON GD OL © DO H& det ped DH oO PLATE IL. Metridia armata. . Male seen from right side. . Anterior antenna of male. . Mandible and palp. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of third pair. . Fifth pair of feet of male. . The same seen laterally. . Fifth pair of feet of female. . Abdomen of female. . Terminal spine of swimming foot. Beas. eal 4 / Z A SEZ: A ae « SS = ©} 2 PLATE V. Dias longiremis. Female seen from right side. . Anterior antenna of female. . Right anterior antenna of male. Left anterior antenna of male. . Posterior antenna. . Mandible and palp. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Fourth swimming foot. . Terminal spine of the same. . Fifth foot of female. . Fifth pair of feet of male. . Abdomen of female. Plate Ss de hee ] GAINS) | LOG aan S & Cle) oP WS DO KF PLATE VI. Temora velow. . Male seen from right side. . Anterior antenna of female. . Fifth foot of female. . Terminal spine of swimming foot. . Abdomen of female. Diaptomus Castor. . Male seen from above. . Anterior portion of anterior antenna of male (“ Westwoodi’’). . Anterior antenna of female (“ Castor’’). . Fifth pair of feet of male. . Fifth pair of feet of female (‘* Westwoodw’’). . Inner branch of fifth pair (“ Castor’’). . Abdomen and extremity of thorax of female (“ Westwoodti’’). . Abdomen and extremity of thorax of male (‘* Westwoodw”’). ile Plate Ge SSS SSS << os Hy Ky} b hi i ¥ 4 vi \ \ POPE EA RYE EN cena = | Stat WWest & C2 imp. MNCS Brady del ; : AT atk coh. : emora velox. iaptomus castor PLATE VII. Pseudocyclops crassiremis. Right anterior antenna of male. . Left anterior antenna of male. Isias clavipes. . Male seen from right side. . Left anterior antenna of male. Right anterior antenna of male. Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . First foot. . Fifth foot of female. . Fifth foot of male. . Terminal spine of swimming foot. . Mandible and palp. yclops crassinervis. clavipes. W. West & C° imx PLATE VIII. Centropages typicus. Fig. 1. Female seen from above. . Right anterior antenna of male. . Apical joints of left anterior antenna of male. . Posterior antenna. . Mandible and palp. . Posterior foot-jaw. . Terminal spines of swimming foot. . Third swimming foot. . Fifth foot of female. . Fifth pair of feet of male. SMO ON DS Oo Bh W DO oa Centropages hamatus. 11. Right anterior antenna of male. 12. Terminal spines of swimming foot. 13. Right fifth foot of male. Candace pectinata. 14. Posterior antenna. 15. Anterior foot-jaw. SRTTT TT ST SEE _—s OTT ee a ee 5 A SS Dae < 1a. Fie. PLATH TX: Parapontella brevicornis. . Male seen from above. . Right anterior antenna of male. . Left anterior antenna of male. . Posterior antenna. . Mandible and palp. Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . First swimming foot. . Third swimming foot. . Fifth pair of feet of male. . Fifth foot of female. . Terminal spines of swimming foot. . Abdomen of male. . Second and third segments of female abdomen seen from behind. . Abdomen of female seen from side. y / ag GSBrady del. f WWest & Comp. ATFoUieh bith | | Parapontella brevicornis. Fig. PLATE X. Candace pectinata. Right anterior antenna of male. . Hinge joints of the same. Anterior antenna of female. Mandible and palp. . Maxilla and palp. . Posterior foot-jaw. Fourth foot. . Terminal spine of same. . Fifth pair of feet of female. . Fifth pair of feet of male. . Abdomen and last thoracic segment of male. . Abdomen of female seen laterally. Anomalocera Patersonu. . Maxilla and palp. 14. Anterior foot-jaw. cS r—1 cD) ==) 6) oy O. ma == 5 fe ONSKSemaet ae Candace 13,14, Anomalocera Pate o, te. l ees G.SBrady del AT. dollick Gith. 45) Siebert on (oe oe Ss Ig A ot ts he Oa / i ee ie ie 7 it PLATE X A. Pontella Wollastoni. Fig. 1. Anterior antenna of female. 2, Anterior antenna (right) of male. 3. Posterior antenna. 4. Mandible. 5. Mandible-palp. 6. Maxilla. 7. Anterior foot-jaw. 8. Posterior foot-jaw. 9. Left foot of fifth pair, male. 10. Right foot of fifth pair, male. 11. Foot of fifth pair, female. 12. Abdomen of male. (The figures in this plate are taken from the work of Dr. Claus, ‘ Die frei-lebenden Copepoden,’ &c.) pages sulle ayes W West & Co ap 3 Pomtella Wollaston. oe ee m © Do = © Con oar ON PLATE XI. Anomalocera Patersonit. . Male seen from right side. . Right anterior antenna of male, with eye. . Left anterior antenna of male. Anterior antenna of female. . Posterior antenna. . Posterior foot-jaw. . Terminal spine of swimming foot. . Fifth pair of feet of male. . Fifth foot of female. . Spme of same more highly magnified. . Abdomen of female seen laterally. . Caudal segments of female. . Caudal segments of male. . Rostrum and lateral eyes. (eg his Meee W West he Co tnp. Anomealocera Patersonii Wie. 14. PLATE Alt. Pseudocyclops obtusatus. Male seen from right side. . Right anterior antenna of male. . Left anterior antenna of male. . Posterior antenna. . Mandible and palp. Maxilla. Anterior foot-jaw. . Posterior foot-jaw. . Foot of first pair. . Terminal spine, &c., of swimming foot. . Fifth pair of feet of male. . Foot of fifth pair of female. . Abdomen of male. Pseudocyclops crassiremis. Fifth pair of feet of male. Plate 12. (ree Q O) iZ zm Yf, \. yy) ie: NUE: EZ AeEP AZ BB i = ey, S) 1-13,Pseudocyclops obtusatus. Te he 14 Crassiréemis. | “iy A Lad Ae el} Fig. O ONO Ob WD 1/6 i. 13. 14. 15. 16. PLATH XITt. Lophophorus wmsignis. . Anterior antenna of female. . Posterior antenna. . Mandible. . Mandibular palp. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of fourth pair. . Foot of fifth pair. 10. Abdomen and tail. Misophria pallida. Anterior antenna of female. Posterior antenna. Anterior foot-jaw. Posterior foot-jaw. Foot of fifth pair. Tail. Plate 13. \ \ s yy / Wz ZiN y) Ve os AE Bolick th. 1-10, Lophophorus imsignis. West eatnep. M16, Misepbriasgolli day Fig. Oo ONT HD Oo LP W DW PLATE XIV. Oithona spinifrons. . Rostrum. . Anterior antenna of female. . Posterior antenna. . Mandible and palp. . Maxilla (?). . Anterior foot-jaw. . Posterior foot-jaw. . One of swimming feet. . Abdomen and last thoracic segments of female ; (a) fifth foot. Porecise rc WoWest % Co.tmp. Oithona, spinitrons. Fig. © CON OS O PR WS DW 10. 1d: 12: 15. 14. PLATH XY. Cyclopina littoralis. . Female seen from left side. . Anterior antenna of same. . Posterior antenna of same. . Mandible and palp. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Fifth foot. . Caudal segments. Lophophorus wnsignis. Female seen from above. Cyclops affinis. Anterior antenna of female. Fifth foot. Tail. Part of one of tail sete, more highly magnified. Pe huoreyailioe WWact & Coir Bro ea. aoe Oye opis Echo aii. 10. Lophophorus insignis. l1-14.Cyclops affinis. pr Fig. PLATE XVI. Thorellia brunnea. . Female seen from left side. . Anterior antenna of same. . Anterior antenna of male. . Posterior antenna. . Mandible and palp. . Anterior foot-jaw. . Posterior foot-jaw. . Swimming foot, one of third pair. . Last thoracic segment, with fifth pair of feet and first two abdominal segments. ee 3 = =~ 2 Plate 16. a AD q iS 5 wa me! a = Thorell a ag a renee eer peers eee ee ee eee ee eee a a a ge ee ee ee Tn le a —— | — a TO et aes oo Se oe ee ee OS Oe oe eer ee SSS Sa ae = = 7 = a 5 ay 5 ie = : ; ; 3 re Spee J eye 7H = fest: 7 z * peg Wie. a. © CO NT oo Gr PLATE XVII. Cyclops pulchellus. Female seen from above. . Anterior antenna of same. . Foot of fifth pair. Cyclops signatus. . Anterior antenna of female. . Anterior antenna of male. . Posterior antenna. . Mandible and palp. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of fifth pair. . Abdomen and tail. oe rte a2 a: /} we LY oy ZA iy ne 1-3, Cyclops gulehellus. tae 43 signatus. PLATE XVIII. Cyclops tenwicornis. . Female seen from above. . Anterior antenna of same. . Mandible and palp. . Maxulla. . Anterior foot-jaw. . Posterior foot-jaw. . Fifth foot. . Caudal segment and setz. . Anterior antenna, penultimate stage of de- velopment. 10. Labrum. Fig. O ONO Oo L&W DS = Misophria pallida. 11. Maxilla. 12. Mandible and palp. mace asec. : Sh pa isoparia Fig. SIO Oo PB OD = PLATE XT Cyclops strenuus. . Anterior antenna of female. . Mandible and palp. . Labrum. . Anterior foot-jaw. . Foot of fourth pair. . Foot of fifth pair. . Abdomen and tail. Cyclops equoreus. . Female seen from above. . Anterior antenna of male. LO. Maxilla. PYate 19. TRANS): _ = aes Oi Eieeds Fins we sy seequore _ aah — ena nar en ~l ne ~~: cet eecuntie renee ET See eS ie a ee Te, 2 ee, me i aan — aa a - 7 z a = r Ww ‘i =e Se : a - ‘ { % 7 = i f : a - sg : a " 3 ; ‘ . . ay ’ = r = : : : : { : aos = ‘ “meee ne ; y 5; er 4 f i - , ’ , = $ \ { = - it] i ‘. =¥ i ig . _ ‘a “ ¢ ; 2 — 1 " } ' a é . . f ¢ ’ | k ry mh ' ai t a t a . > ‘4 ag GON & Oo S & DO ot Oo © PLATH XX. Oyclops gigas (adult female). . Anterior antenna. . Mandible and palp. Labrum. . Maxilla and palp. . Anterior foot-jaw. . Posterior foot-jaw. . Fourth foot; apical joint of outer branch. . Fourth foot; apical joint of inner branch. . Fifth foot. . Abdomen and tail. The same, penultimate stage of development. hie 12. 13, 14. 15. 16. Anterior antenna. Mandible and palp Posterior foot-jaw. One of swimming feet. Fifth foot. Abdomen and tail. WWest & Cop. Ne ee SSS MINS SEE MA es > lops $1243. C ) DP 2 ‘ @ miei es = o es eee Le ee s 7 2 at se na gr Se ee ee Se a eo te et (rE ~ BESS gece ee PS ney ee ge ol . mm emerges Say eee ei oo gi: te ta aes — Fig. PLATE XXVI. Notodelphys agilis. . Female, adult. . Male, adult. Anterior antenna of female. Anterior antenna of male. . Posterior antenna. . Maxilla. . Posterior foot-jaw. . Foot of first pair. . Abdomen and fifth pair of feet of male. 10. Foot of fifth pair, female. — . \ \ CO er : oy >» y/ . S e LS ie yl 7 : . — eo N lay BK : a Sis VA‘ : Y\V VA ‘\ } AX) } A) YA\, WED PN EAN YA wa VA At) by WAMU, Wi a= Notodelphys agilis. WW ob fj / WAL ANS 2 Wiss. g LI EE SN = Tas Soe" G.SBrady del. AT Aollick thy. SHY Fig. PLATE XXVIII. Doropygus porcicauda (female). . Adult female. . Anterior antenna of same. Posterior antenna. . Anterior foot-jaw. Foot of first pair. Foot of second and third pairs. Foot of fourth pair. . Foot of fifth pair. . Terminal segments of abdomen C CONT & Or HB Oo DO Notodelphys cerulea (female). 10. Anterior antenna. 11. Posterior antenna. 12. Outer branch of first foot. 13. Fifth pair of feet. Wace. 16.8 Brady da. 3 3 4) = are) 4) x 0 ® R ‘ im = M op mo O O O14 W KN ie a as ea! ~ © Ore o 2 ei) O = ce HOS) ss ae O al AT Ho thick Eth. Pe =" ~ Fig. CON & OF HR ©® PO te NO a a= Lo) PLATE Sy: Doropygus pulex. . Adult female, with ova (after Thorell). . Female, younger. . Adult male. . Anterior antenna of female. . Posterior antenna. . Mandible and palp. . Anterior foot-jaw. . Foot of first pair. . Foot of fourth pair. . Foot of fifth pair. . Caudal segments of female. . Caudal segments and abdomen of male. rece 2. SS Lie SESS EI ne, Se SX SS VEIN AG AY KE W West & Co.twp. Doropygus pulex. Fig. PLATE XXIX. Doropygus auritus (female). . Female with ova (after Thorell). . Anterior antenna of same. . Posterior antenna. . Mandible. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of first pair. . Foot of third pair. . Foot of fifth pair. . Caudal seement. Pista 23. (aia GliGal eae ® Dorepyqus en 14 1 ie 5 Fie. cS OO" SIGs 10. PLATE. AXX: Ascidicola rosea (female). . Adult female. . Anterior antenna of same. . Posterior antenna. . Mandible and palp. . Anterior portion of body. a, anterior antenna ; b, posterior antenna; c, mandible; d, maxilla ; e, anterior foot-jaw; j, posterior foot-jaw ; g, first foot. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of first pair. Foot of third pair. Notodelphys prasina (female). (From Scandinavian specimens sent by M. Thorell.) 4. 12. 13. 14, 15. Anterior antenna. Mandible. Outer branch of first foot. Foot of fifth pair. Caudal and last abdominal segments. Plate oo a —— Vee Se SSS SSSLAQg =< < EE = << IWS= SN SS ee ——— = ROSE 1 — A WSS oe Ws ) \ iO) As cidi@ela, rosea. Il—15 Notodelphys prasina. ha alle wa * +t Fig. 1. PLATE XXXI. Doropygus pulex ? var. Anterior antenna of adult female. . Caudal segments. Notopterophorus papulio. . Female from above. . Female from side (after Hesse). Anterior antenna. . Posterior antenna. . Mandible. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of first pair. . Tail, seen laterally. SSS LES . \ = \ 38) Oo 7) 3 Wes ial Bae Ay | ye ne RS) 8 Q $ eS iS O 4 ene af on Se a r ; BS a ND a6 oP) So @) rane eyes oO So 5) ane ue an Ce oi | oD . ; ih | i i! i RETIN —_ =a Fig. oan oO FP OC LD = et be He © a He © PLATE XXXII. Doropygus Normani. . Adult female, seen from side. . Anterior antenna of same. . Posterior antenna. . Mandible. . Maxilla. . Anterior foot-jaw. . Posterior foot-jaw. . Foot of first pair. . Foot of second pair. . Outer branch of fourth foot. . Foot of fifth pair. 12. . Caudal segments. . Extremity of same, more highly magnified. Marginal spine of fifth foot (highly magnified). PEs Or, «shy Vineeat\ try cane ETN NAW rl NY Ti \ \ 17 GSBrady ole. ae Me) AT Aollice tite. WWest & Co.tmp. Doropygus Normani. ed — & ee GS: BS 14, 15, 16. © ONO ao bh & D PLATH SAXXITT. Botachus cylindratus. . Adult female. Young male ? Anterior antenna of adult female. . Posterior antenna. . Mandible and palp. . Maxilla. . Anterior foot-jaw. . Foot of first pair. . Posterior foot-jaw. | . Foot of second pair. . Foot of fourth pair. a, spine of outer branch, more highly magnified. . Foot of fifth pair. . Tail. Doropygus porcicauda. Mandible, extremity. Posterior foot-jaw. Extremity of tail. ~ Plate 33. \ SS ead as | - WWest & Eoramp. | Lo isikiguaciwus eylindratus. 14-16 D oropygus porcicauda. ! sy isk? ae 7 eee yY DOCIHTY. INSTITUTED 1844. FOR THE PUBLICATION OF WORKS ON NATURAL HISTORY. ANNUAL SUBSCRIPTION ONE GUINEA. Tek Se OF OFFICERS, LOCAL SECRETARIES, AND SUBSCRIBERS, CORRECTED TO JUNE, 1878. OFFICERS. airesident, Siz P. DE M. G. EGERTON, Barrt., M.P., F.R.S. Council, Professor ALLMAN, F.R.S. Sir A. Brapy, F.G.S. Dr. BRAITHWAITE, F.L.S. G. B. Bucxton, Esq., F.R.S. G. Busk, Esq., F.R.S. C. H. Garry, Esq., F.L.S. FERDINAND GRUvT, Esq., F.L.S. R. Hupson, Esq., F.R.S., F.G.S. Professor HUXLEY, F.R.S. 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