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my ' if Sk us , } , H Am. Jour. Sci., Vol. XiV, 1902. Plate |. Fig. 1 Fig. 2 Fig. 3 Fig. 4 THE AMERICAN JOURNAL OF SCIENCE [FOURTH SERIES.] Art. I.—On Spectra Arising from the Dissociation of Water Vapor, and the Presence of Dark Lines in these Spectra ; by JoHN TRowsBRIDGE. (With Plate I.) In passing from the study of the light emitted by gases under the effect of electrical discharges of comparatively small quantity to the investigation of the light produced by dis- charges of great quantity, a new field of research is entered. In previous papers on the spectra of hydrogen, I have stated my convictions of the importance of the role played by water vapor in spectrum tubes. The results of further study emphasize these convictions. With powerful discharges in hydrogen, oxygen, and rarified air, I always obtain the same spectrum, which I regard as that arising from the dissociation of rarified water vapor. The line spectrum, moreover, is accompanied by a faint continuous spectrum on which are dark lines, which indicate a selective reversibility in the silver salt, which is of great significance, it seems to me, in the applica- tions of photography to astrophysics. It has long been recognized that spectrum analysis is an extremely delicate method of recognizing the presence of a gas or the vapor of a metal under the excitation of heat ; and when the improvements in photography enabled us to obtain per- manent records of the spectra of gases, it was supposed that we had a means of escaping from the fallacies of eye observations which arose necessarily from personal idiosyncracies. If the hotographic plate were a perfect instrument for recording the infinite number of vibrations which light can communicate to atoms of matter, we should certainly feel that we had made a great advance in physical science. When we reflect, however, on the belief that emulsions containing silver salts are capable of responding to all wave lengths of light in the portion of Am. Journ. Sci1.—FourtTH SeErizs, Vout. XIV, No. 79.—JuLy, 1902. 1 2 J. Trowbridge—Spectra from the the spectrum considered most actinic, even when the light ex- ceeds a certain intensity, we are conscious that we cannot rely upon an infinite range of photochemical action; and I shall show in this paper the existence of a selective reversibility produced on the photographic plate by powerful discharges of electricity through capillary tubes. Realizing the importance of studying the behavior of gases under different forms of excitation, I have collected in the rooms devoted in the laboratory to spectrum analysis three forms of apparatus: an induction coil actuated by a very eff- cient liquid break, giving a spark of thirty inches in air; a step-up transformer excited by an alternating current, pro- ducing with glass condensers of about °3 microfarad, dis- charges of an inch in length, of great body; and a storage battery of twenty thousand cells. A plant of this nature I conceive to be necessary in the present state of spectrum anal- ysis, for molecular motions excited in rarified gases vary greatly with the kind of electrical discharge.. In the application of photography to spectrum analysis, the investigator is immedi- ately confronted with the necessity of submitting the gas toa comparatively long electrical stimulus in order to obtain a negative. Even with a concave grating of short focus several discharges are necessary with a narrow slit. Hach discharge is capable of modifying the condition of the gas. This fact is well recognized by taking successive photographs of the light emitted by a spectrum tube under different strengths of eur- rent upon the same photographic plate. A simple form of plate holder enables this to be done. One obtains a striking example of the instability of the spectrum tube filled with apparently dry hydrogen when one subjects it first to very powerful discharges from a glass condenser of °6 microfarad, charged by a storage battery of twenty thousand cells, with practically no self-induction in the circuit; and follows this excitation by the use of an alternating discharge of much less quantity. The powerful discharge gives what I term the water vapor spectrum; and after a certain number of these dis- charges one obtains with the alternating current discharges the spectra of argon. This results, I suppose, from the oxidization of traces of air in the tube. The-hydrogen has disappeared momentarily; possibly the dissociation of the water vapor resulted in concealing its presence. The period of the condenser discharges which I have em- ployed varied from one five hundred thousandth of a second to one millionth. The practically instantaneous current varied from five thousand amperes to ten thousand. The revolving mirror method showed that the pilot spark was mainly effect- ive, and that the subsidiary oscillations were feeble. The Dissociation of Water Vapor. 3 spectrum tube speedily became milk white from the sodium set free from the glass. Lord Rayleigh* has shown how to demonstrate the presence of argon from very small quantities of air. My method is sub- stantially his, except that I employ very powerful discharges which set free a sufficient amount of sodium vapor from the glass, and the oxygen is supplied from the dissociation of the water vapor, which is always in evidence when such powerful discharges are employed. The production of argon under these circumstances is a striking proof that I am dealing in this investigation with the spectrum of the dissociation of water vapor. From the same tube one can, by modifying the strength and character of the electrical discharges, obtain what is termed the four-line spectrum of hydrogen, the spectrum of sodium, the spectrum of argon, and the spectrum of the dis- sociation of water vapor. Doubtless one could also recognize the spectrum of helium; I am not yet sufficiently familiar with it. In the course of a study of the water vapor spectrum one is naturally led to photograph the spectrum of the electric spark under water. It is possible to obtain powerful discharges of any snitable Jength under distilled water by enclosing the spark terminals in glass tubes, allowing only a small portion of the platinum terminals to project from the ends of the tubes. If the terminals are immersed more than an inch under water, the resulting explosion is apt to break the glass-containing vessel. The light of these discharges under distilled water is white and extraordinarily brilliant to the eye. When it is ex- amined by the spectroscope one sees a continuous spectrum ; and one obtains a continuous spectrum even by photography in the most actinic portion of the spectrum. On bringing the spark terminals to the surface of the water, leaving them barely immersed, one immediately obtains the so called four-line spec- trum of hydrogen. ‘To what is due the continuous spectrum under water? Does it result from the production of the water vapor spectrum under great pressure? ‘That there is great pressure is shown by the sudden explosion, which is sufficient to blow the small tamping of water out of both ends of the containing tube. If the surface of the water is covered with a thin film of oil, this oi] is immediately disseminated through the water, a milky white emulsion, which remains for days. When we turn to powerful discharges through Geissler or Plucker tubes filled with hydrogen which has been dried with great care, we also obtain a continuous spectrum on which are superposed the bright lines of the water vapor spectrum, together with certain reversed lines, giving on the positive * Phil. Mag. (6), vol. i, 1901, p. 103. t J. Trowbridge—Spectra from the dark lines instead of bright lines. Moreover, what are ap- parently the strongest bright lines of the water vapor spec- trum are not reversed. There is aselective reversibility which arises with high temperatures, and is made evident by the faint background of the continuous spectrum. ; This fact seems to me to be of great importance in the appli- cation of photography to the study of celestial phenomena, for reversal of spectrum lines do not necessarily indicate reversing layers of cooler gas, and may be a photochemical action of the silver plate. One immediately thinks in this connection of the phenome- non of dark lightning or the Clayden effect, and of the sug- gestive experiments of Professor Nipher.* Spectrum analysis, however, reveals a selective reversibility, which shows that the subject of photochemistry must be carefully studied before we can interpret properly the records of photography in spectrum analysis. There are doubtless many states of vibration even in the actinic portion of the spectrum which are not recorded by the silver salts, for a selective reversing action may obliterate or prevent a permanent record. I have obtained this reversing action with different emul- sions on glass and also on celluloid films. The strongest reversals are at wave lengths 4227, 3930, 3965. There is also a reversed band between wave lengths 4315 approximately and 4285, and a faint reversal at wave length 3953. Rever- sals are often seen on the negatives which disappear in the fixing bath.+ In this investigation ten thousand storage cells were em- ployed to charge a glass condenser of ‘60 microfarads. The charge was sent through Geissler tubes having an internal bore of one millimeter; the length of the capillary of this diameter was from eight to ten centimeters. The tubes were filled with apparently dry hydrogen at a pressure of approximately -1™™. I have reached a limit in submitting gases in glass tubes to powerful electric discharges, and am now turning my atten- tion to the subject of quartz tubes in the hope of obtaining these in a suitable form for containing rarified gases. In a previous paper,t I have expressed my conviction that the four-line spectrum observed in the protuberances of the sun is an evidence of the dissociation of water vapor in the sun’s atmosphere, and an evidence therefore of the presence * Transactions Academy of St. Louis, vol. x, No. 6, On certain properties of light struck photographic plates. + In this connection the following paper is significant: Disappearance of images on photographic plates. William J. S. Lockyer, Nature, Jan. 17, + This Journal, vol. x, Sept. 1900. Dissociation of Water Vapor. 5 of oxygen. In the spectrum one sees two reversed bands which coincide with the great H. H. lines in the solar spece- trum; one also sees a reversed line at wave length 4227, closely coincident with a strong solar line; one has also a reversed band coinciding with a region of reversals in the sun between wave lengths 4315-4285. These regions in the sun are doubt- less composite photographs of many reversals of different ele- ments. I believe, however, that the basis of the reversals is the presence of dissociated water vapor. The nomenclature, too, of the stars in relation to their spec- tra I believe should be changed to dissociation spectra; an excess of water vapor produces what is termed the hydrogen type, and the dissociation of this water vapor in the presence of other gases, nitrogen for instance, together with metallic vapors, may account for other types. The intense light due to the dissociation of water vapor may, in some cases, mask the fainter light of the metallic lines in the stars which show only gaseous spectra, especially when we consider the varying distances of the stars. J have em- ployed electrodes of platinum, copper, silver, aluminum, iron, and aluminum, and no trace of the lines of their vapor can be perceived in the photograph of the gaseous dissociation spectra ; moreover, when sodinm is present in the spectrum tubes, although it fills the tube with a brilliant yellow light at low voltage and strong currents, and exhibits the sodium lines very strongly, no trace is seen of it, with very powerful discharges. The tubes then show only the brilliant white light due to the dissociation of water vapor: a light which is the nearest ap- proach to sunlight which I have been able to produce. Its actinic effect is greater than that of any of the metals, such as magnesium, aluminum or zine. Possibly the varying amount of water vapor may be a factor in the variability of certain stars; and one is led to conjecture whether the light of the sun’s atmosphere is not due to an electrical dissociation due to discharges of very high period. The selective reversibility of the silver salts seems to me of momentous importance in the subject of astrophysics; for we have reversible actions on the photographic plate which are not due to the radiations of a gas passing through colder layers of the gas. In other words, we have actions recorded which are photochemical and are not in the heavens. It may be that certain reversals observed in the spectrum of Nova Persei may be of this nature. This selective reversibility serves to reveal certain lines which escape observation. Thus we see that there is a gaseous line at wave length 4227, and a line not shown on the reproductions but clearly seen on the negatives between the great H. H. lines, having a wave length of 3953. 6 WS. Trowbridge—Spectra from the Dissociation, ete. The silver salt, therefore, does not respond to all rates of vibration ; or if it does respond, the molecule is unstable and there is no resultant reaction which is evidenced by a photo- graphic image. There may be spectra at very high instan- taneous temperatures which we cannot phctograph. It seems reasonable to suppose that the silver molecule is limited in its rates of vibration and that the photographic plate as well as the human eye is a limited instrument of research. : On Plate I, A represents the solar spectrum in the neighbor- hood of the great H. H. lines. B represents the gaseous spec- tra. The photographs were taken with a Rowland concave grating, and are not enlarged or touched in any way. Unfor- tunately the reproductions do not give many of the reversals, Figs. 1 and 2, B are spectra of air and oxygen taken with a comparatively low voltage and amperage at a pressure of about one millimeter. Fig. 3 is a spectra of hydrogen under the same conditions. Fig. 4 is the spectrum arising from the dis- sociation of water vapor with very powerful discharges. Fig. 5 shows a selective reversal line at approximately 4227. On the negative the two bright gaseous lines, which in fig. 4 closely coincide with the great H. H. lines, are seen to be reversed and appear as dark lines. This reversal is shown in fig. 7. B of fig. 7 closely resembles in general features the solar spec- trum when the latter is photographed with a broad slit, so as to obliterate details and give broad characteristics. My conclusions are as follows: Dissociation of water vapor takes place in the atmosphere of the sun; oxygen, therefore, must be present. From a carefal study of my negatives, I regard the evidence for the presence of water vapor as conclusive as that accepted for the presence of sodinm in the sun. The dissociation of water vapor, under the effect of power- ful electric discharges in the presence of small amounts of atmospheric air, results in the production of argon even in tubes presumably filled with dry hydrogen. The spectrum arising from the dissociation of water vapor contains dark lines as well as bright lines. These dark lines are due to a selective reversibility of the silver salt employed in the photographic emulsions, and are not due to the reversing action of a cooler layer of gas. The great brilliancy of the dissociation spectrum of water vapor, which obseures the spectra of metallic vapors: and the presence of dark lines due to photochemical reversals, make one cautious in accepting photographic evidence in regard to states of development of stars. Jefferson Physical Laboratory, Harvard University, Cornwall— Greenockite on Calcite from Joplin, Mo. 7 Art. Il.— Occurrence of Greenockite on Calcite from Joplin, Missouri ; by H. B. CoRNWALL. | A YELLOW coating of greenockite on the sphalerite of the Joplin zine district is no uncommon occurrence, and having received, through the kindness of Messrs. Geo. L. English & Co., of New York, specimens of calcite from this locality which showed a very distinct greenockite coating, the writer made tests upon the material, to determine what proportion of cadmium sulphide the coating might contain. The greenockite occurs as a bright yellow, dust-like coating, which can be easily rubbed off with the finger. Beneath the greenockite coating, and often extending beyond it, there is, for the most part, a brown or yellowish brown, more adherent deposit, in a thin layer which can be easily scaled off with the knife-point. This seems to be sphalerite. The greenockite was removed by very gentle scraping with the knife and subjected to the tests below. Although in places it is very distinct, the coating is also very light, and from an area nearly two centimeters square not more than 0-0014 grm. of the purest material could be obtained. Even this portion was found to be mixed with zinc compounds from the scale-like deposit below it. Gently roasted on platinum foil over a Bunsen flame, the powder on cooling was brown in some parts, and nearly white (distinctly yellow while hot) in others, indicating cadmium and zine oxides.* The roasted powder, mixed with an abundance of charcoal dust and heated to moderate redness in a closed glass tube, gave a brownish sublimate (cadmium oxide), and on stronger heating a less volatile sublimate, yellow while hot, white on cooling (zine oxide). On roasting 0:0014 grm. in a small platinum dish, dissolving the residue in sulphuric acid, evaporating and gently igniting, a residue was obtained which weighed 0°002 grm. Theory requires from pure cadmium sulphide 0:00202 grm. of cadmium sulphate; but as a mixture of sphalerite and calcite similarly treated might give the same figures, this result does not indicate with any certainty the proportion of cadmium in this lot of material. A second lot, also weighing 0°:0014 grm., was dissolved in nitric acid, evaporated to dryness with sulphuric acid, and heated to expel all free acid, the residue treated with a single drop of hydrochloric acid, sp. gr. 1:20, and dissolved in four * When not too strongly heated at first, the yellow coating assumes a transient dark brown or reddish-brown color, and becomes yellow again on cooling. ! 8 Cornwall—Greenockite on Calcite from Joplin, Mo. cubic centimeters of water. The whole was then saturated with hydrogen sulphide gas, giving very quickly a yellow precipitate, and this, after letting the gas act long enough, was filtered off, dissolved in strong hydrochloric acid, evaporated with sulphurie acid, ignited and weighed as sulphate. By this means the coating tested was found to contain 23-07 per cent of cadmium, or 29°66 of cadmium sulphide. It should be said that the coating yields sulphur dioxide when roasted. By comparing the liquid holding in suspension this cad- mium sulphide with another in which a known amount of cad- mium sulphide had been precipitated, it had already been estimated that the yellow coating on the calcite contained not less than 15 per cent of cadmium. Finally, although the Joplin sphalerite on which greenockite occurs will give a distinct reaction for cadmium when roasted and reduced with charcoal in the closed tube, in the manner already described, yet it was found that no precipitate could be obtained from it by hydrogen sulphide, even after thirty minutes action, the treatment being quantitatively, and in every other respect, exactly the same as described for the yellow coating on the calcite. A mixture corresponding to a sphalerite containing 5 per cent of cadmium yielded a precipi- tate of cadmium sulphide, under identical conditions, in a few minutes. Dana (System of Mineralogy, 6th ed.) states that the amount of cadmium present in any sphalerite thus far ana- lyzed is less than 5 per cent. It therefore appears certain that this yellow coating on the calcite, like that on the Joplin sphalerite, is greenockite. John C. Green School of Science, Princeton University. Cumings and Mauck— Variation in the Fossil, ete. 9 Art. IIIL.—A Quantitative serials of Variation in the Hossil Brachiopod Platystrophia lynz;* by EpGar R. Cumines and ABRAM V. Maucr. (With Tinine II and III.) DuRinG the year 1900-01 the authors made extensive collec- tions of the brachiopod Platystrophia lynx from the Upper Ordovician rocks at Vevay, Indiana (Switzerland Co.). Inasmuch as this species is extremely variable and at the same time exceptionally abundant and well preserved, a quan- titative study of the variations presented at once suggested itself. Such an investigation is the more warranted because of the different opinions current as to the taxonomic importance of several of the forms under which Platystrophia presents itself. The specimens used in this investigation were collected from a zone which at Vevay extends from 240 ft. to 360 ft. above the level of the Ohio River. Part of the material was so col- lected that the precise layer is known from which a given specimen came; the object being to determine as accurately as possible the factor of range.t The majority of the specimens used are from the upper 50 or 60 feet, and the upper 20 feet contains by far the most as well as the best of the material. Examples could not be obtained in sufficient abundance from the base of the Platystrophia zone to make a quantitative treatment possible; but we were able to ascertain that in the lower part of its range at Vevay, and in general throughout the Ohio Valley, Platystrophia presents less variation than at higher horizons ; and that in the lower beds only the small pauci-plicate form is present.§ Beside the material collected layer by layer, a large collec- tion was made from the upper beds wherever exposures could be found in the vicinity of Vevay. The data taken for study are: Ratio of width to length of shell (equals shell index); ratio of depth to breadth of sinus * Presented before Section E at the Denver meeting of the American Asso- ciation for the Advancement of Science, August, 1901. + For synomony and bibliography of Platystrophia see Davidson, Silurian Brachiopoda, 1871, p. 268; Hall and Clarke, Pal. N. Y., vol. viii, pt. i, pp. 200, 201; Schuchert, Am. Foss. Brachiopoda, Bull. U. S. G. S., No. 87, pp. 308-310. ¢ The Vevay section is published in the Am. Geol., vol. xxviii, Dec., 1901, pp. 361-381. By reference to page 373 of that paper it will be seen that the lowest specimens of Platystrophia (associated with Dekayia ulrichi) are small and of a type similar to var. laticosta or var. dentata Meek (crassa James). The form lynx does not come in till within 30 or 40 feet of the top of the sec- tion. § Specimens have been examined from these lower zones at Cincinnati, Ohio, Lawrenceburg, Aurora, Rising Sun, Vevay and numerous points on Laughery Creek in Indiana. 10 Cumings and Mauck— Variation in the (equals sinus- index); number of plications on ventral valve ; number of plications on dorsal valve; number of plications in sinus; number of plications on fold. 4 The width of the shell is in every case the greatest width, whether this occurs at the hinge line or farther forward. It was obtained by means of adjustable spring calipers. The width of the sinus was obtained by spreading the points of spring dividers between the anterior lateral angles of the sinus. The depth of the sinus was obtained by spreading the points of the dividers from one anterior lateral angle of the sinus to the anterior extremity of the first adjacent furrow in the bot- tom of the sinus. All measurements were read off on a milli- meter scale and are correct to within 0°25™™. The number of shells used varies for the several characters indicated above, on account of imperfect material. Only entire shells were used for measurements; but the number of plications, especially the number in the sinus, may frequently be determined with accuracy on very poorly preserved speci- mens. The number of shells used in determining any one sharacter is called a group. Group I, Shell Index. Width divided by length. Number of shells used, 679. Range of variation from 1:0 to 1:8. Modet at 1°3, with fre- quency of 300-4.{ Variation here is moderate in amount, and — in the direction of greater width than length. Group IL, Sinus Index. Width of sinus divided by depth of sinus. Number of shells used, 664. Range of variation from 0-9 to 3:0. Mode at 1-7 with a frequency of 112-2. Variation great in amount, and in the direction of a shallow sinus. Group ITI, Number of Plications on Ventral Valve. Number of shells used, 1173. Range of variation from 10 to 28. Mode at 17 with a frequency of 176°3. Variation large in amount, and in the direction’of the greater number of plications. * Prof. Shaler has given (Foss. Brach., Ohio Valley, p. 48) a series of meas- urements of a limited number (20) of specimens of Platystrophia. His series includes also forms from Richmond, Indiana, and other American localities. In a forthcoming paper I shall take up the discussion of material from all the provinces both American and European, where Platystrophia is known to oceur.—E. R. C. + The term mode means the highest point of the curve, i. e., the class with the greatest frequency. t Forthe purposes of comparison all frequencies were Teduced tofreqtencies ~ per thousand. 0968-0 |9TET| | = | | | | | | | | | | | | I | F | CP | SSI | 988 | 0g | A dnorp 6802-0 |STFT a: Je! 0) i OFC re0t 881 Te) AT dno SUIONHNOMU YT ALATOSay { . ns. Sera Se eee cole elle |68-0 99-8 |e9-28 [P9-eeTles-eoul6c-2e |e6-L1) A dnorg IPL |PO-F |TL-68 |1S-FLTIGT-GeL/16-98148-FL| AT dnory a aes lear el Neen Pagers, all: 8 hi 9 ¢ i 8 S I SOSSVTO ‘GNVSNOH YT, UAd SHIONDTAOAU YT F GLIe-% |ISh ‘a ae & g E Geleoa nor a | 14v | 09 | 06 | 7 | of | @ | ge | i ee I | | MIIT dnoay C6G8-0 [GATT LG es 20s On Tee hog) | Gens enh) air | kom] tet | eet 19 he ke ole ee | TT dno ‘SHIONGNOUUY ALATOSAYy 1-8/18-% |eP-F |eh-P [99-9 |0G-ST/SL-LT/LF-GE|F9-L6|18-FOT|G0-EET|GC-661|GL-611/98-OTLIG1-86 leP-ce |6g-F% l08-EL |Te-2 w{TT Inoay G8- OL-T |OL-T |LT-G |6G-8 |06-LT|FS- 18/68-0G|80-ST1/6P-STL6G-CET9F-9LT/06-OST|TP-LOLILP-eP |T¢-48 196-4 |9¢-F |e9-0 | IT dnory TOCi Ieee Ce Caro ete aoe eres Ole | Bi Yh.) Or: | op | Fr: | ere are anon Sassy) ‘ANVSOOHY, Ud SHIONTOAOAU 090¢-T [p99 | I [ | Lc |e | 0 | ¥ | 9 | 88 | | & | 09 | 69 | Pe | 4 Op) Fen| een cae | 9 | g Il dnosy LOLD-T_|6L9 Ab ae | Ge See 23 GE LO PPL | POEs) - TAL eg li I dnotp Q ears ‘SHIONT OOM, GLA TOSTY a B ° re ey SB | «8 (09. 1|0G-1/10-€/F0-21/L¢-61|@1-08|29- 1e/GT-68|@e-4C/6L-GL'TS- 81/9806 |16-G0T/6-C11/26-90T|8L-0L |F8-09 [0%-1¢ |eT-¢8 [$0.6 [80-6 | &-F TL dnory om | 85 | 6-6 08-OF |PS-1¢ |29-86 |90-818/SF-008|¢9-998|96-G¢ |LF-T ] dnoip Po 0 GieOmieeelemcsindcel Gcdleterl tra CC IeenicOe Ore el (kek Ot | OT | pL ete let | TT 10-1 | 60 SO8SR1O a3 | 2 $113 eee He & ‘GNVSQOHY], UAd SHIONTAOAUT le) (7) 12 Cumings and Mauck— Variation in the Group Illa, Plications on Dorsal Valve. Number of shells used, 451. Range of variation from 11 to 29. Mode at 18 with frequency of 199:°55. Variation corre- lated with that of Group III. Group IV, Plications in Sinus. Number of shells used, 1412. Range of variation from 1 to 7. Mode at 3 with frequency of 729-1. Variation in the direc- tion of the larger number of plications. Group V, FPlications on Fold. Number of shells used, 1116. Range of variation from 2 to 8. Mode at 4, with a frequency of 793°8. Variation precisely correlated with that of Group LV.* The complete data are charted on page 11. The method of ; constructing the curves of fig. 1 is the usual one of laying off the classes along the axis of abscissas and the frequencies along corresponding ordinates. The lack of correspondence between Groups III and Ila, which should be exactly correlated, is due to the relatively small number of specimens used in Group Illa. It forcibly emphasizes the necessity of using as large series of specimens as possible. All the curves are skewed. None of them show more than one mode. They all rise abruptly and fall off less abruptly. This shows a certain correlation of the different variants. An attempt was made to determine the relation of the num- ber of plications in the sinus to the number on the entire valve. Hallsays: ‘*The prevailing number of lateral plica- tions is seven on each side of the sinus or lobe; and so long as the mesial plications remain three and four, so long the lateral ones are seven. As soon as there is even an appearance of a departure from this number on the mesial lobe and sinus, and where the rudiment of an additional plait is visible, we then find the lateral plaits to be nine or ten.” t Our material does not bear out this statement. ‘To test the point it was assumed that there is a precise correlation between number of plications in the sinus and number of plications on the whole valve. The area of the freyuency polygon for any given number of plications in the sinus should then be equal to the sum of the areas of the frequency polygons of a definite number of plications on the valve. For example, the frequency polygon of three to four plications in the sinus has an area equal to that of the sum of the areas of the frequency * While there is necessarily one more plication on the fold than in the sinus, the fact that many specimens, owing to state of preservation, can be used for the determination of one group that are not available for the other, makes the two groups supplement each other. + Hall, Pal. N. Y., vol. i, 1847, p. 134. ———— ee a Fossil Brachiopod Platystrophia lynx. ae Es: polygons of seventeen, eighteen, nineteen, and twenty plica- tions on the ventral valve. Therefore any shell with four plications in the sinus should have between seventeen and twenty (both numbers inclusive) plications on the valve. It should have no more and no fewer. An inspection of our material does not show this to be the ye tv b eve OV IIla III Fieg 1. Curves of Groups I to V. On the axis of ordinates, each small division represents four individuals. On the axis of abscissas, each fifth (as from a to b) represents one class. ease. In a series of 153 specimens with four plications in the sinus, the range is from 16 to 26 plications on the ventral valve. The average is 18°8 plications. The specimens with two plications in the sinus have from 11 to 22 plications on the valve. Those with one plication in the sinus have from 10 to 15 on the valve. The correlation is approximate rather than precise. , II 14 Cumings and Mauck— Variation in the An inspection of Plates II and III shows the small size of the extreme forms, and conversely the large size and robust growth of those forms near the modes. The largest specimens will not be found exactly at the mode in any of the characters for which curves are plotted, but in classes to the right of the mode. That is, while it is true, for example, that by far the majority of specimens have three plications in the sinus, the largest specimens are more likely to be found in classes having more than three plications in the sinus. They will never be found in classes having less than three plications. When, how- ever, the class falls some distance to the right of the mode it will again be found to contain small specimens. Smallness of size is, therefore, an accompaniment of the general extinction that prevails more and more, away from the mode. In the case of the number of plications on the valve, extinction does not become severe till the 20th is reached; and in the classes between 17 and 20 will be found the largest individuals. In regard to the validity of the several species or varieties into which the dynz group of forms has been divided, namely, Platystrophia lynx, P. laticosta, P. dentata Meek (= P. crassa James), there is absolutely no character or combination of characters that can be relied upon to separate any large col- lection into distinct species. To a limited extent the above forms differ in range; although the authors have frequently seen all three represented on a single slab of limestone. It is well, however, to distinguish for stratigraphic purposes such varieties as laticosta, and dentata Meek.* The following is a description of the modal form of Platy- strophia lynx: shell three-tenths wider than long; greatest width about half-way from the hinge line to the front of the shell; width of sinus seven-tenths greater than its depth; seventeen angular plications on the ventral valve, three of which are in the sinus; eighteen on the dorsal valve, four of which are on the fold. * As stated in a preceding footnote, the other forms, acutilirata Conrad, biforata Schl. and other foreign forms of Platystrophia are not considered in this paper. The form identified by Miller, and doubtfully by Meek, as dentata Pander is the costata of the latter author. Pander has figured dentata and costata (= chama Eichwald) side by side on pl. xi of his Beitrage ~ zur Geog. Russ. Dentata has two plications in the sinus and three on the fold, while costata has one in the sinus and two on the fold. The name chama Eichwald cannot be retained for this variety, since the Spirifer cos- tatus of Sowerby is a true Spirifer, and there is no other prior use of the name costata among the Orthide. See de Verneuil Geol. de la Russie, p. 140, and Sowerby, Tr. Geol. Soc. Lond., 2d ser., v, pl. lv, fig. 5-7. On the vari- eties of Platystrophia see especially Meek, Pal. Ohio, i, 1878, pp. 112-121; Hall, Pal. N. Y., i, 1847, pp. 133-1384; Winchell and Schuchert, Minn. Geol. Surv., iii, 1893, pp. 454-457; Davidson, British Silurian Brachiopoda, 1871, p. 268 et seq. ; Schuchert, Bull. 87, U.S. G.S., p. 308; Sardeson, Am. Geol., xix, p. 109. ‘OSVO TOVS UL SuUOTZVOTTC JO TOG MANU 0} AoJor SONY oY} MOlOd SLOquINNT “POF WO SUOTZVOTT ‘OAISNPOUL Ge 07 LZ ‘SSI ‘“SNUIS UL SUOTZVOTTd ‘OATSHPOUL OY 07 OY “SSL ‘“OATVA [RIZUOA UO SUOTZVOTTA ‘OATSHPOUL GT O} T ‘SST nal Tan) 4 L 9 G p @ g V 9 C( wm wow qa WY 8 ee ite 08 6e 8¢ Le 9% rd > OG ; > ie) o AiG ) NO = G p @ g i 8g Le 92 n> S s va) & WZ WW) Ss _ * Ry 7 eg ra 12 0% 61 ST Ni = & GB i GB 8 Ie 08 61 81 nS ~ SO : VW Q ~ RQ > % 9T Cy a SI ra iA Or 6 it 91 CT val eT ral ia OT 8 L 9 G v g z I ‘Tl Bavig yove Ul XOpUl OY} JO ONT[VA Yj SAIS selnsy oy} MOloq s1equInNy = QD D ~sS "~ va) (a) Ss oe D < &.3 ‘= i) ; ES Ss oe S re NK 1. ee 2 S << @Y BS = 91 a ~ hel ~: = = SS) 16 0-€ ND GG ! WD &G V1 AW) 6-6 al Yes) = 8-6 0-6 ‘TIL Sivitd LG QD "XOPUL SNUIS ‘OATSN[IUL TE OF OT ‘SST 9-6 61 0-1 "OsBo ‘XOPUL [JOYS ‘OAISN[OUL G OF T ‘SOLA LS a 9% von Coe OG dail On ST Fe 6-0 8.7 OT 6 Tal 0-T z ji Wortman—Studies of Eocene Mammalia, ete. a7 Art. IV. — Studies of Eocene Mammalia in the Marsh Collection, Peabody Museum; by J. L. WortTMAN. [Continued from vol. xiii, p. 448.] Sinopa minor sp. nov. A SMALLER species is represented in the Marsh collection by numerous remains, all in a somewhat fragmentary condition. Of these, I select as the type a_consider- able portion of a man- dibular ramus of the right side, contain- ing the three pos- terior premolars and the first and second molars in place, fig- eee ure .96. Thereisalso FIGURE 96.—Right lower jaw of Sinopa minor the anterior part of Wortman; side view; natural size. (Type.) the opposite ramus, which contains the root of the canine and those of the anterior premolars. With this, I associate as a cotype a fragment of a right upper jaw bearing the fourth premolar and first molar, figure 97. The characters of this species, as exhibited by the type and cotype, are as follows: The size is much smaller than either S. rapaz or S. gracilis ; the canine is of the usual pro- portions; the small single-rooted first pre- molar is implanted some distance behind the _ FicuRe 97.—Frag- : : 2 ment of aright upper canine, and is separated from it and the jaw of Sinopa minor second premolar by considerable diastemata; Wortman; crown the second premolar is two-rooted and sepa- View; natural size. rated from the third by a short interval, (Cot?) differing in this respect from both S. rapax and S. gracilis ; the third and fourth premolars have the usual form ; the first molar is relatively small, with low trigon and a large basin- shaped heel; the second molar is larger, with high trigon and large heel; the internal cusps are but little reduced, differing in this respect from S. gracilis and agreeing with S. rapaw ; the last molar is not preserved in the type; the fourth superior premolar is like that of S. gracilis, except that the internal cusp is more conical; the postero-external blade exhibits faint traces of a bilobed condition, which is not seen in SV. gracilis ; the two main external cusps of the first molar are well separated ; there is a more distinct posterior intermediate, and an internal cingulum, all of which are different from S. gracilis. Am. Jour. Sci.—FourtsH Serizs, Vou. XIV, No. 79.—Juny, 1902. 2 96 18 Wortman—Studies of Eocene Mammalia in the There are three or four individuals that agree perfectly with the type and cotype, but there are others that have a heavier build and are perceptibly larger. I cannot detect any further differences in the materials at hand, however, which would warrant referring the latter to another species. It may be that more complete specimens will necessitate their separation. Additional characters derived from these specimens are: Second lower molar equal to, or slightly larger than, third; last superior molar without postero-external cusp, and second superior molar, as well as first, with distinct internal cingula. The measurements of the type are as follows: Length of inferior dental series from base of canine, exclusive of ‘lastmolar. 2 0007. oo 4. ee ee 42° mm Length. of ‘pnemolars-.22 222 280. ee | Be eee 30° Length of first _and second molars .._-.--. 5-222. fae 12° Length of entire inferior dental series (estimated) ..-- - -- 48°5 Antero-posterior diameter of first molar._....-...---2-. © Antero-posterior diameter of second molar _---_.-------- os Antero-posterior diameter of third molar (not type) ----- 64 Measurements of Cotype. Length of fourth premolar and first molar __.......----- 18° Antero-posterior diameter of fourth premolar_....-..-.. © Antero-posterior diameter of first molar.._...--.------- di Transverse diameter of fourth premolar. ...-.---------- 5° Aransyerse diameter of first molar: /2_550-.. 40‘) 25a 4°6 The type specimen was found by Professor Marsh, at Griz- zly Buttes, and the cotype, by Mr. Kinney, at the same locality. Other specimens are from Church Buttes, and one is doubtfully from Henry’s Fork. Sinopa major sp. nov. The last species of this group to be considered is the largest yet found in the Bridger horizon. It is apparently unde- scribed, and the above name is proposed for it. Two reason- ably complete mandibular rami, figures 98, 99, one of which contains nearly all the teeth in place, together with three or four other fragmentary pieces carrying various teeth, repre- sent it in the collection. The type specimen has the three molars and the third and fourth premolars in place in the jaw, together with the roots and alveoli of the remaining premolars. The chief characters of the species, as exhibited by this speci- men, may be stated as follows: It is much larger than S. edaz, S. gracilis, or S. minor ; the second premolar is separated but very slightly, if at all, from the third; the first is small, single- rooted, and placed about equidistant from the canine and second premolar; the second molar is slightly larger than the Marsh Collection, Peabody Museum. 19 third; the heels of the molars are large and basin-shaped, that of the last bemg smaller than the other two; the shear is rather transverse, and the internal cusp is less reduced than in S. gracilis ; the jaw is much more massive and deeper, and the distance from the posterior base of the canine to the third premolar is proportionally shorter than in the other species. This indicates a rather short-muzzled type. The specimens 98 FIGURE 98.—Right lower jaw of Sinopa major Wortman; side view; nat- ural size. (Type.) 99 FIGuRE 99.—Left lower jaw of Sinopa major Wortman ; side view; three- fourths natural size; restored from three specimens. suggest an animal intermediate in size between a red fox and a prairie wolf. The principal measurements are: Length of inferior dental series from posterior base of canine 70°™™ SemermetmpmeBBOL AES 2-2 2 2 ee bee eee eek 44° Peer IMMeE AIS SS 558 ies Joes e+ = 4+ = --- 26° Antero-posterior diameter of first molar___----.--------- 8: Antero-posterior diameter of second molar.--.----------- 10° Antero-posterior diameter of third molar ._--.-----.------ -F Peo: jaw at sceond molar ____-...2_-_-.-...------- 20° Meaieos jaw at. second premolar__.-.....-_.----------- 16° The type specimen was found by Sam Smith at Church Buttes. 20 Wortman—Studies of Eocene Mammalia in the Discussion.—Two other species of this genus, aculeata and insectivoru, were described by Cope from the Bridger, but Matthew has shown* that the types are unrecognizable, and he suggests that the names be dropped. That the Bridger species should be more advanced than those of the Wind River and Wasatch is quite natural. At least three of them thus far known do not show any very great advance in structure over their older representatives, but still enough to separate them specifically. The remaining one, S. pas exhibits very decided progress in the direction of the igher specialization of the family. This is seen in the disap- pearance of the posterior external cusp of the third superior molar, the more decidedly connate condition of the two main external cusps of the first and second superior molars, the development of a more sectorial structure of the fourth pre- molar, reduction in size of the heels of the lower molars, and reduction of the internal cusps of the trigon, with a more longitudinal shear. The internal cusps of the upper molars are also reduced. There appears to be very good evidence of the specific descent of this species. Thus, Sinopa hians of the Wasatch, as far as its structure is known, answers with tolerable accu- racy to the ancestral requirements. Sinopa Whitie of the intervening Wind River horizon appears to be intermediate in | every feature of its osteology, as far as known, with the single exception that the second lower premolar is not spaced. If this character were variable in the Wasatch species, 1t may well prove to be the annectent form. That Hyenodon and very probably Pterodon, also, were derived from this group, there appears to be very little doubt. The fundamental similarity in the structure of the skull, teeth, vertebrae, pelvic girdle, limb bones, and carpus, cannot be acci- dental parallelism, but on the contrary affords very strong pre- sumptive proof of genetic aftinity. The most specialized species of the genus, Sinopa agilis, however, cannot be in the line of direct descent because of the relatively small skull and the sharp, compressed, and slightly fissured, bony claws ; whereas in Hyenodon, at least, the skull is large in proportion to the skeleton, and the claws are flat and deeply fissured. It should be noted here that nearly every specimen of the genus Sinopa represented in the Marsh collection comes from the lower part of the Bridger beds, and that not more than one or two have been found in the upper part of the horizon. Their complete absence from the Uinta, as far as we now know, is, moreover, fairly satisfactory proof of their extinction *Bull. Amer. Mus. Nat. Hist., Jan., 1901, p. 24. ’ Marsh Collection, Peabody Museum. 21 or migration from this country at the close of the Bridger. For this reason, I am persuaded that the evolution of the Oli- gocene types took place probably in Asia or the north, during later Eocene time, and that their subsequent appearance in this country during the Oligocene was due wholly to migration. It is highly probable that some generalized Wasatch species, such as S. opisthotoma of Matthew, was the ancestral type from which they were derived. Further Observations upon the Marsupial or Metatherian Relationship of the Creodonts. In the foregoing descriptions of the various characters of the Creodonts, frequent reference has been made to their rela- tions with the Marsupials. Objections will doubtless be raised to the use of this term, since some writers restrict the term “ Marsupial” to the living representatives of the group, which is perhaps, strictly speaking, correct. Huxley proposed the term Metatheria for a hypothetical group, which was meant to include both the modern Marsupials and the immediate Impla- eental forerunners of the Eutheria. The all-important dis- tinction of such a group would consist in the implacental method of its reproduction—a character which would at once separate it from the Eutheria, in which an allantoic placenta is formed. In like manner, the absence of a distinct coracoid, the union of the odontoid process with the body of the axis, the lack of oviparous habits, and the more highly developed reproductive system would distinguish it from the Prototheria. Unfortunately there are no known characters of the skele- ton in this group which are constant associates or infallible correlatives of the implacental mode of reproduction, and since, among the fossils, we are compelled to depend solely upon osteological evidence, our judgments must of necessity rest very largely on analogy. When I have spoken of “ Marsupial characters” and “ Marsupial relationship,’ I have had con- stantly in mind the Implacental Metatheria of Huxley, prefer- ring the use of the term “ Marsupial,” because the large number of primitive characters exhibited in the living members of this group undoubtedly furnish us the safest ouide tor a proper interpretation of similar characters in the fossils. By taking the more primitive members of the existing Marsupials as the basis of our comparisons, | am convinced that we shall be able to arrive at a very much clearer understanding of what the ancestors of the Creodonta were like, than by any other method of study. That they were der ivatives or offshoots of any pre- existing group of Placentals or Eutherians is exceedingly unlikely, and the strongest evidence of this fact is that they are practically as low in the seale of organization as any known 22 Wortman—Studies of Hocene Mammalia in the Eutheria. Moreover, evidence of the existence of such a group remains to be discovered. On the contrary, all the facts point very strongly to their origin, along with the Carnassidentia, from Implacental or Marsupial Metatherians. It is likewise conceivable that from this same general substratum the other Eutherian orders arose. Some day, when our knowledge of these matters is vastly more extensive and accurate than at present, it will perhaps be necessary to abandon this horizontal system of classification, implied by the use of such terms as Prototheria, Metatheria, and Eutheria, and substitute for it the phyletic or linear sys- tem—the only one expressive of the genetic relationship which we seek to discover. It will then be determined, without much doubt, that these several ordinal groups have recogniz- able chains of ancestry, penetrating not only well down into the Metatherian substratum, but almost to the very bottom or beginnings of Mammalian existence. We shall then give names to these lines of descent rather than to successive stages of their development. But until this Utopia in the subject is realized, we must content ourselves with cruder methods, more in keeping with our ignorance. Summary. Having now completed a study of all the Eocene Carnivora in the Marsh collection, I append herewith a brief summary of the more important discoveries, opinions, discussions, ete., embodied in the foregoing paper. They are the following: The general organization of the order and the relationship of its more primitive members to the Metatherian Marsupials are discussed ; the order is divided into three suborders, Creodonta, Carnassidentia, and Pinnipedia, and their relations are con- sidered ; of the Eocene Canide, the type of the genus Vul- pavus is figured, a new species added, much of its osteology described, and the progressive modification of the family con- sidered; a new related genus, Veovulpavus, is proposed ; addi- tional characters of Uintacyon, together with its position in the group, are given; Prodaphenus is considered to be the forerunner of the Amphicyon series, and four main lines of canine descent are pointed out; the Viverravide are defined, the type species of Viverravus is figured, and another species added; a new genus of this family, Oddectes, is proposed and a large part of its osteology described ; the relations of the Viverravide to the living Viverride are examined, .and the position is taken that the descent of the modern civets is prob- ably traceable to this source; the type species of the three genera T’riacodon, Ziphacodon, and Harpalodon, are figured, and the opinion expressed that they are not valid genera; the Marsh Collection, Peabody Museum. 23 type of “Alurothervum is figured and described, a new species added, and its ancestral relationship to the Felidz discussed and reaffirmed ; the organization of the Creodonta and their relations to the Metatherian Marsupials are considered, a new classification is proposed, and the families are redefined; the Viverravide and Palzeonictidz are removed to the Carnassi- dentia ; the family Mesonychide is considered, the genera of the Mesonychine are defined, a new genus, Harpagolestes, is proposed and defined, and the osteology of Dromocyon vorax given in full, with numerous illustrations; the small pelvic outlet may have indicated extreme helplessness of the young at the time of birth, like the Marsupials, and a possible cause for the extinction of the line; the evolution of the phylum is con- sidered, and the progressive modifications of the teeth and limbs are pointed out; the origin and homologies of the mam- malian tritubercular molar are fully discussed, and dissent is expressed from the theory of Migration or Rotation of Osborn ; the family Oxyznide is considered, the arrangement of the genera discussed, and two subfamilies, Oxyzeninee and Limno- -eyoninee, are proposed and defined; the genera of the Oxye- hinge are defined, the type specimen of Patriofelis ferowx is fieured and described in detail, and the probable habits of the species are rediscussed at length; the genera of the Limno- cyonine are defined, one new species is added, and the synon- ymy of the others given; many new points are added to a knowledge of this group, its possible Insectivorous relation- ship. is pointed out, and one species, at least, is thought to have been aguatic in habit; the family Hyzenodontide is redefined, and the Bridger species of Stnopa, of which two are added, are described in detail; much of the osteology of Sinopa agilis, with illustrations of skull, fore foot, and limb bones, is given ; the probable origin of the Hyzenodonts and Pterodonts is con- sidered, some further observations on the Marsupial or Meta- therian relationship of the Creodonts are made, and their probable origin is considered. 24 P. EF. Schneider— Eruptive Dikes in Syracuse. Art. V .—New Exposures of Eruptive Dikes in Syracuse, NYS by Pe rite Sci nmin: | Igneous rocks in the horizontally stratified Paleozoic beds - of Central New York are too rare to pass unrecorded; and when, recently, excavations in Syracuse for the Butternut street trunk sewer disclosed another of these occurrences in a new locality and at so great a depth that ordinary excavations had not reached it because of the thickness of the overlying drift, it became important that some permanent and available record _ should be made of the same. The eruptive rock was first noticed April 16, 1901, some three days after it was first penetrated. At this point, a short distance beyond the place where the sewer crosses Highland st., the eruptive rock occurred in the bottom of the trench and was dug into only to a depth of some two feet. It was over- laid by nearly three feet of decomposed peridotite, which had been entirely changed to a soft greenish-yellow earth. As the excavation progressed to the east of Highland st., the work- men penetrated deeper into the rock, which for some distance presented a slightly stratified appearance suggesting a sheet branching from the dike proper, which subsequent excavations proved to be the case. The dike itself was first encountered 126 feet east of the center of Highland st., and was so hard and firm as to be removed with great difficulty. The width of the dike is 36 feet and it comes up to within ten feet of the natural surface. From its location in the trench, which was five feet in width, the strike of the dike appeared te be N..5° EB Wier ae scarcely any sheet to the east of the dike, but to the westward it extended over three hundred feet. The rock in the main dike, with the exception of the upper two feet, is perfectly hard and firm. It is of a dark green color, some of it being almost black, and contains an abund- ance of apparently jet black crystals. The upper ‘portion, immediately beneath the drift, had changed to a soft greenish- yellow earth, in some places to a yellowish earth. The fact that the lower portion of. the drift contained much of the serpentinous earth mixed with it would suggest that a con- siderable area was covered with eruptive matter. The typical rock contained few inclusions as compared with that at De- Witt, N. Y., or even that in the Syracuse dikes at Green st. The softer rock of the sheet, however, contained many of them. No prominent fossils were found in any of these inclusions, whereas in the rock at De Witt they were very P. F. Schneider—Eruptive Dikes in Syracuse. 25 abundant. No traces of the enclosing walls of the dike could be found. Sheet material banked it on the west, and heavy Pleistocene clays with quicksand beyond them formed the eastern border. At Green st. the enclosing walls are perfectly shown, and it was hoped that further excavations would open up other exposures showing the contact phenomena, but this did not oceur. ‘The other excavations, where the strike of the dike would seem to indicate its existence, were all on higher ground with heavy mantles of drift which even this deep sewer did not penetrate. _ One other opening occurred in a return sewer on Highland st. The excavations passed for 180 feet through rock which was thought at that time might be merely sheet material from the dike, but I am now convinced that it was another parallel dike. This rock, while almost as difficult to excavate as that of the first dike, decayed very rapidly after a few days expo- sure. It also had more or less of a massive wedged appearance in the trench like the first dike, and quite unlike the banded appearance of the sheet, and furthermore contained many inclusions. It also contained numerous small red crystals, the “rubies,” which the neighboring school children collected in abundance. None of these peculiar forms were found in the De Witt, or in any of the Syracuse dikes at Green st. Some of them appeared to be perfectly crystallized garnets, but so rapidly did this rock break up, especially when dry, that they usually fractured soon after being exposed. A few crystals of greenish color were also obtained from this same rock, but none of either kind were noticed in the hard, firm variety. All of these facts would seem to indicate a second dike more or less parallel to the first and less than 250 feet away. Through this second dike the excavations must have passed very nearly longitudinally, while the sewer proper erossed the main dike at nearly right angles. As the return sewer stopped when connection had been made with the sewer proper, and as the excavations up to this point did not pass through to the farther side of the dike, no facts as to its width can be given. The proximity of these dikes to those at Green ‘st., which are less than a mile away, suggests some under- ground connection, and inasmuch as their general direction is the same they may be merely a continuation of those dikes. The intervening space has frequently been trenched, and at such times the excavations have been carefully watched for evidence of the dikes without revealing any trace of them. Syracuse, N. Y. 26 Smyth, Jr.—Petrography of Dikes in Syracuse, N. Y. Art. Vil.—Petrography of Recently Discovered Dikes in Syracuse, V. ¥.; with Note on the Presence of Melilite in the Green Street Dike; by C. H. SmytuH, Jr. THE freshest specimens of the dike rock from Butternut st., Syracuse, N. Y., are nearly black, but in the average material the color is gray, with a more or less decided greenish tinge. In tex- ture, the rock is distinctly porphyritic, with phenocrysts ranging up to 15™™ or more in diameter, scattered somewhat unevenly through a moderately fine and even-grained groundmass. Occasional veinlets and small pockets of calcite appear, but these are exceptional, and the rock as a whole, aside from the “ sheet ” material mentioned below, is quite homogeneous. Of the specimens sent to the writer for examination, many appear to the unaided eye quite fresh and unchanged from their original condition; but they are very deceptive, as in most eases alteration has progressed to a considerable degree. Sev- eral sections cut from sound specimens of good color and with lustrous dark phenocrysts, under the microscope show little but a mass of alteration products, which, however, retain the original texture of the rock very well. In consequence of this alteration the following description of the petrography of the dikes is based upon only a few sections of fresh material, together with such data as are afforded by the altered speci- mens. But the petrography is comparatively simple, and the data at hand are sufficient to show a substantial agreement with the other dike rocks of the vicinity. Sections of the least altered material show that the pheno- crysts are olivine, as indicated megascopically. Crystal outline is generally lacking or at most quite imperfect, and the irregular grains show the customary alteration to serpentine along cracks | and around the margin. In some grains this alteration is but slight, while in others the serpentine has wholly replaced the olivine. Between the two extremes there is complete grada- tion. Associated with the olivine there is a very little colorless monoclinic pyroxene. It occurs in irregular grains, and shows the usual high extinction angles. Though in very small amount, this pyroxene is a fairly constant constituent of the rock. Biotite of a pale brown tint appears in large irregular plates and shreds of small size. The former are primary, but the appearance of the shreds and their relations to the other min- erals suggest that they may be, in part, secondary. Perofskite is abundant, though varying considerably in quantity in dif- ferent sections. It appears in minute crystals of sharp outline. In some cases, high powers show these crystals to be octahedra, — Smyth, Jr.—Petrography of Dikes in Syracuse, N.Y. 27 and this is probably, as would be expected, the form of all of them. They are honey yellow, and decidedly translucent, so much so indeed as to show this property clearly with low powers. In this respect, the perofskite differsfrom that of the De Witt dike, in which Prof. Kemp* perceived the translucent character only with high powers. It would be difficult to find better microscopic specimens of perofskite than are shown in the rock here described. Magnetite is another primary mineral, occurring in the usual small crystals and irregular grains. But it is far less abundant than is often the case in rocks of this general type. In some sections there is ‘a small quantity of a granular, isotropic min- eral with high index of refraction. While this may be garnet, no exact determination of the species could be made. In addition to the foregoing minerals there is present, even in the freshest specimens, a considerable amount of undeterminable alteration products mingled with the serpentine, carbonates, secondary magnetite, mica shreds and the minor primary constitnents to make up the groundmass. While it is possible that there may have been glass in the unchanged rock, none is now recognizable. Much of the foregoing description of the freshest parts of the dike applies equally well to the more altered parts. In these, the olivine has been almost wholly changed to serpentine, which is greenish or yellowish and shows the characteristic net texture to a marked degree. The double refraction of the serpentine is very low, and in the thinnest parts of sections, and often elsewhere as well, it is sensibly isotropic. Different specimens show great diversity in the amount of secondary magnetite in the serpentine. In some cases the former min- eral is scantily sprinkled through the latter, while in other cases the serpentine is rendered nearly opaque by the powdery magnetite. The primary magnetite and perofskite are not affected by alteration, the latter in particular retaining all of its characteristic properties and showing in the sections of thoronghly altered specimens perhaps even better than in the fresher rock. All of the foregoing changes belong to the process of alteration rather than weathering, and do not affect the integrity of the dike as a whole, while modifying its com- position, both mineralogical and chemical, to an unknown depth. Weathering on the other hand, though superficial, destroys the dike, as far as it goes, resulting in thorough disintegration. The rock first called a sheet, but now regarded as probably a distinct dike, differs from that described above chiefly in con- taining abundant inclusions of the wall rocks together with * This Journal (3), xlix, p. 459. 28 = Smyth, Jr.—Petrography of Dikes in Syracuse, NV. Y. occasional grains of garnet. The inclusions are so numerous as” sometimes to equal or exceed the dike rock in quantity, and it is probably due to their presence that the rock goes to pieces very rapidly when exposed to the atmosphere. This may be due in part to the chemical effects of the inclusions, but more largely to mechanical influences, the homogeneity of the rock being destroyed, while it is filled with fragments, many of which disintegrate easily. The material is most unsatisfactory — for study and affords very poor sections. The following description is, for this reason, quite incomplete. The garnet appears rather scantily in irregular, rounded grains, sometimes reaching 4 or 5™™ in diameter. The color is bright red, becoming very pale in thin sections. Around most of the grains there is a very thin shell somewhat distinct from the rest of the rock, but the nature of the material is such that no good section of the shell could be obtained. Apparently mica (perhaps with hornblende) is the chief constituent. In one case the sliell consists of decomposition products, through which are scattered great numbers of perofskite crystals. Somewhat analogous to this is the occurrence of a mass some 3™" in diameter consisting largely of tiny crystals of perofskite, the whole surrounded by a shell of biotite. In every case seen by the writer, the garnet occurs in that part of the rock which contains abundant inclusions, but never in the inclusions themselves. This relation to the inclusions, together with the scantiness and irregular distribution of the garnet, suggests that rather than a normal product of the dike magma like that of the Elliot Co., Ky. peridotite described by Diller* and that of many European occurrences, it may result from the fusion of parts of the wall rock in the molten dike, somewhat as in the case of the sapphires of Yogo Gulch, described by Pirsson.t However, conclusive evidence upon this point is lacking. That the garnets are themselves inelu- sions derived from the wall rocks is hardly possible. Were this the case, garnets should be found in some of the inclusions themselves, and even did this happen, it would be needful to prove that they were primary, and not formed by the contact action of the dike rock. Moreover, the only external source of garnets would be in the underlying pre-Cambrian rocks, and these are of such a nature that they would be most unlikely to fuse completely away from the garnets, leaving the latter free. Embedded in one of the garnets was a bright green grain about 0°5™™ in diameter. When broken and placed under the microscope it shows one cleavage, with which the extinction makes'a high angle, while the green color is hardly perceptible. * Bull, 38; UNS Gs; + This Journal (4), iv, pp. 421-428. Smyth, Ir.—Petrography of Dikes in Syracuse, N.Y. 29 The mineral is probably pyroxene, but the limited quantity hardly admits of accurate determination. Aside from the variations described, this rock differs in no marked degree from the first dike rock described, except that one section shows tiny prismatic crystals of pyroxene in the groundmass. On account of its excessive alteration, sections of the rock are largely made up of secondary products, but these are essentially the same as those described above. Of the two classes of inclusions, Paleozoic and pre-Cambrian, the former are naturally more abundant. ‘The fragments are often angular and sometimes show a faint zonal coloration along the contacts. But there is no decided indication of new mineral growth. ‘The pre-Cambrian fragments are usually more rounded, the result of the attrition involved in their upward journey of many hundred feet. They do not differ materially from inclusions described in other dikes of the region. | In comparing the rocks of this locality with specimens from DeWitt and from Green st., as might be expected, a strong family resemblance is apparent. There is perhaps less mica and rather more perofskite in the Butternut st. rocks, while only one section shows the tiny crystals of pyroxene that are so abundant in the groundmass of the DeWitt dike. But these differences are much too slight to be of any moment. Melilite in the Green St. Dike.—The marked resemblance, both in petrography and geological relations, between the Syracuse rocks and the alnoite of Manheim has led the writer to expect, at any time, the discovery of melilite in the former. In studying the DeWitt rock, Prof. Kemp* searched carefully for this mineral but found none. The writer’s study of the Butternut st. rock met with the same result; but in the exami- nation of the rock of the original Green st. dike of Williams,t melilite was found. This seems at first sight surprising, as, doubtless, sections of the rock have been examined by many petrographers ; but the fact that melilite has not been noted before simply illustrates the elusive naturé of the mineral, resulting from its tendency to alteration. In the case of the original Manheim dike, the rock was first described by the writer{ as a peridotite and its true nature was learned only when fresher material was procured ;§ while in the largest dike of that locality no melilite could be determined with cer- tainty, although there can hardly be a doubt of its original presence. | Some years ago a section was made from a specimen of the Green st. dike which very closely resembled the original * Loe. cit. + This Journal (3), xxxiv, pp. 1387-145. t Ibid. (8), xliii, pp. 322-327. § Ibid., xlvi, pp. 104-107. || Bull. Geol. Soc. Am., ix, pp. 257-268. 380 Smyth, Jr.—Petrography of Dikes in Syracuse, NV. Y¥. Manheim rock and, moreover, seemed fairly fresh. This was searched, with greatest care, for melilite, but to no purpose. In the present study, three sections of the rock have been - examined, one from an old specimen and two from new material. In the first, a few very small individuals of melilite were found, so inconspicuous that their discovery can be regarded as little more than accidental. But in the other two sections, the melilite. is present in some quantity. In habit and general appearance it is very like the Manheim melilite, though less abundant. Like the latter, it often shows abnormally high double refraction, possibly the result of alteration, and, as a rule, is optically positive, although the negative variety is also present. From the foregoing, it is evident that in rocks as thoroughly serpentinized as are those of the Syracuse dikes, melilite may be nearly or quite obliterated; and it is extremely probable that perfectly fresh specimens would show melilite in all of these dikes. Perhaps an exception should be made in the case of the DeWitt dike, but even here there would seem to be sufii- cient alteration to mask the melilite if originally present in small quantities. Apparently, then, the petrographic affinities of this group of dikes is with the melilite rocks rather than with the peridotites, and this is interesting in bringing them into close relationship with the Manheim dikes, and in deter- mining another occurrence of a rare variety of rock. Of course, incomparably the most important contribution to our knowledge of the Syracuse rocks was the establishment by Williams* of their igneous nature, but all new data in regard to the locality are worthy of record. In a note appended to his description of the De Witt dike, Prof. Kempt givesa brief resumé of the occurrences of igneous rocks in Central New Y ork, including two instances of bowlders. Another case of the latter kind may be mentioned here. In the Hamilton College collection are two specimens labelled “ Hornblende Boulder, Syracuse, N. Y.” The rock is coarsely porphyritic, with very little groundmass, and so peculiar in aspect that the writer had a section made from it some years since. Under the microscope this shows idio- morphic pyroxene of pale violet color, with a somewhat smaller amount of olivine. The individuals of both range up to 10-12"" in diameter, and the two minerals make up perhaps 90 per cent of the rock, being held together by a scanty ground- mass of minute laths of plagioclase. While it is quite possible that the rock is of Canadian origin, still it may well belong with the other bowlders referred to, in a group of basic erup- tives breaking through the New York Paleozoic rocks. Hamilton College, Ciinton, N. Y. * Op. cit. and Bull. Geol. Soc. Am., i, pp. 533-084. + Op. cit., p. 462. Steiger—Silver Chabazite and Silver Analcite. 31 Arr. VII. — Preliminary Note on Silver Chabazite and Silver Analcite; by GEORGE STEIGER. In an investigation upon the constitution of certain silicates an attempt was made to replace the alkaline metals by silver. This has been done with chabazite and analcite, the only two species upon which, so far, I have been able to test the reaction. It will at once be seen that this work is analogous to that of Heumann* and others in the preparation of silver ultramarine. Heumann, by heating blue ultramarine in a sealed tube to 120° for fifteen hours, obtained a silver salt which was very nearly pure, and which upon fusion with various chlorides and iodides yielded corresponding compounds of barium, zine, manganese, etc., and also compounds of some organic radicals. The first experiment which I attempted was to heat ammo- nium chabazitet in a sealed tube with five times its weight of silver nitrate for four hours at 250° C., at which temperature the silver nitrate easily fused. After leaching with water, a determination of silver was made in thedried residue, 25:06 per cent Ag,O being found. Another portion was boiled for several hours in an open dish with a 10 per cent solution of silver nitrate; the residue from this gave 17:20 per cent Ag,O. These results show that ammonium was at least in part replaced by silver. The experiments upon chabazite were only preliminary, and are to be carried farther. More complete work was done in the case of analcite, and three portions of it were treated as follows: “A.” Natural analcite heated in an open tube with dry silver nitrate for four hours to 400° C. “B.” Natural analcite heated in a sealed tube with dry silver nitrate for four hours at 250°C. “C.’ Ammonium analcite,t heated in a sealed tube with dry silver nitrate four hours ‘at 250° ©. All were leached with water, and washed until the filtrates gave no test for silver; the residue was then dried on the water bath. The product in each case was a white powder not differing in appearance from the original material. The analyses of the different portions are given below, together with the composition of the theoretical compound Ag,O-Al,0,48i0,-2H,O, which is found in column “ D.” * Liebig’s Annalen, cxcix, 253 (1879). + This: Journal, vol. xiii, p. 27. t This Journal, vol. ix, p. 117. 32 Steiger—Silver Chabazite and Silver Analeite. A. B. eh D. Leach water Na,O (cale. to analcite)-. 13°13 12°57 - 60 Dried residue S10, ici wipe k Pea bate aban inne: WM 41°31 40°08 42°69 aE! has ts) Al,O, SEP ik, MEMEO Ce Pie Seah 16°44 . 16°29 18°22 1b:72 ‘CANE ea Sinead MRI et® _ 87:45 3691 . 32°01 38°03 NAMP SP en ea ees "85 8] “68° "> a BE 8) On 4-29 5°86. 6:08 5°90 NMR St cy 2) re a eee Se: Bape | ‘69 NO a MO Gr Aves oie eek es none none none 100°34 99°95 100°37 100°00 It seems from the foregoing experiments that at least some of the natural silicates, which have been supposed to be very refractory bodies, are easily attacked and replacements effected by simple operations. Work is now in progress on other minerals, along these same lines, and it is also proposed to study the action upon them of thallinm and lead nitrates and other salts. Chemical Laboratory, United States Geological Survey, Washington, D. C. O. H, Hershey—Cretaceous Outliers in California. 33 Art. VIII—The Significance of Certain Cretaceous Outliers in the Klamath Region, California ; by OscAR H. HERSHEY. CRETACEOUS remnants occur in the southern part of Trinity County, California, in five very limited areas. They are dis- tinguished from the Neocene deposits by their better lithifica- tion, by the gravel being almost exclusively of quartz and displaying the marine type of rounding, by their occupying structural basins and not valleys of erosion, and by their being identical lithologically with the Cretaceous deposits in the neighboring portion of the Sacramento Valley. The principal Cretaceous outlier is in the valleys of Indian, Redding and Brown’s Creeks, a few miles northwest of Bully Choop peak. It is about three square miles in area, and elon- gated in a direction west-southwest. It consists of several hundred feet of fine, well-stratified, yellowish sandstone and a little of the olive-colored shale so characteristic of the Upper Cretaceous in the Sacramento Valley. It rests unconformably on the Abrams mica schist. The next area is at the junction of the North Fork of the East Fork of Hay Fork with the main East Fork Creek. It occupies less than a square mile in area, but dips distinctly toward the center of the small basin. The lower bed is a coarse, mixed breccia and conglomerate. The angular frag- ments were derived from the underlying Paleozoie slates and cherts. This bed differs from the usual basal conglomerate of the Cretaceous in the Sacramento Valley, but its identification is made certain by its being overlaid by the olive-colored shales, whose characters are tinmistakable. The third area occurs on the divide between Hay Fork and Salt Creeks, at the head of Dobbin Gulch. There is about a thousand feet of coarse conglomerates with some green sand- stone, yet the deposit is only about one square mile in extent. On all sides it dips distinctly toward the center of the basin at angles between 20° and 30°. It rests on Paleozoic slates and cherts, the Clear Creek volcanic series and the Bragdon slate, the latter of very late Jurassic age. The pebbles, cobbles and occasional bowlders which compose the rock are, however, chiefly of white, yellow, brown, pink, blue and black quartz, derived from the rocks of the Klamath region bunt at some dis- tance from their present position. The fourth remnant occurs at the junction between Rattle- snake and Post Creeks and is about one and one-half square miles in area. It rests on the Clear Creek volcanic series, and Am. Jour. Scl.—FourtH Series, Vou. XIV, No. 79.—JuLy, 1902. 3 34 O. H. Hershey—Cretaceous Outliers in California. consists of several hundred feet in thickness of a fine pebbly conglomerate, overlaid by a coarser conglomerate. The peb- bles in the first are of quartz, have a remarkable uniformity in size and are perfectly rounded. They weather out and bestrew the surface as would a shower of marbles. They unmistakably indicate marine action. Another supposed Cretaceous remnant is found at the - Sweepstakes mine, a few miles southwest of Weaverville, but it has not been studied in detail and its extent is not known. It consists of a hard conglomerate of fine pebbles resting on the edges of the upturned Paleozoic slates and cherts. The first four areas are Horsetown in age. The differences which are observed between them in going southwestward are exactly imitated by the basal beds of the Horsetown from the village of Horsetown along the foot of the mountains to Har- rison Gulch and Good’s Pass. At Horsetown the basal beds are shale and fine sandstone, as in the Indian Creek area. To make the identification complete, both Diller and Anderson have found the Horsetown fauna on Indian and Redding Creeks. Westward from Ono, the basal bed of the Horse- town is a heavy conglomerate like that of the Dobbin Gulch area; and near Harrison Gulch, there occurs in the Cretaceous the same peculiar pebble conglomerate as that of the Post Creek area. Undoubtedly the sea of the Horsetown epoch transgressed on the southeastern border of the Klamath region and deposited probably several thousand feet in thickness of conglomerates, sandstones and shales over what is now a rough mountain area. At the time of the submergence it must have been compara- tively even, but the heavy conglomerates tell of elevated and perhaps mountainous land in the interior of the Klamath region. This country, that became covered by the Horsetown sedi- ments, had previously suffered profound denudation. At the close of the Jurassic period, the stratified and already largely metamorphosed formations of Mesozoic, Paleozoic and perhaps earlier age, were intruded by three great series of batholiths, the first of peridotite, the second of gabbro and the last of granodiorite and allied plutonic rocks. These intrusions were: accompanied by orographic activity of the greatest magnitude, for the whole area was thrown into a series of geosynelines, with many minor folds and faults. At the close of the dis- turbance the surface must have been very mountainous—a mountain system, in fact, made up of quite different and more massive ranges than those of to-day. Erosion slowly reduced these mountains. Most of their destruction was accomplished during the early Cretaceous time. Several thousand feet at O. H. Hershey— Cretaceous Outliers in California. 35 least of Mesozoic slates and meta-andesites were removed and the rivers cut deeply into the Paleozoic slates beneath. The denudation reached even to the plutonic masses and laid bare the coarse-grained gabbro and granodiorite which must have solidified at a considerable depth beneath the surface. As products of this erosion and of that accomplished in the Sierra Nevadas at the same time, we have in the Coast Range region many thousands of feet of sandstone and shale, the first chiefly Franciscan and the latter Knoxville in age. Judging from the work performed, this “early Cretaceous” period must have been a very long one, perhaps equal to all the time since. Base-leveling in the Klamath region continued through the Horsetown and Chico epochs. Northeastward from Horse- town the Chico formation laps past the Horsetown and from Clear Creek to far beyond the Sacramento River it is in con- tact with the metamorphic rocks as shown by Diller and others. The basal. bed of the Chico is a fine sandstone, with no conglomerate whatever present in this area. Apparently the southeastern border of the Klamath region had been pretty thoroughly base-leveled before the opening of the Chico epoch, but the northeastern border seems to have still remained hilly, since the base of the Chico in Shasta Valley and the Siskiyou range is a heavy conglomerate. It is probable that even to the close of the Cretaceous, the central portion of the Klamath area remained elevated, but base-leveling had been affected around its borders, and a very slight depression was sufficient to cause the Upper Cretaceous strata to lap over on to it. Subsequently to the Chico epoch there occurred another profound orographic disturbance of the Klamath region. It was characteristically different from that which closed the Jurassic period. Much of the area and perhaps all seems to have been deformed into a series of deep, elliptical basins. The four principal Cretaceous remnants in Trinity County mark the deepest portions of four of these structural basins, each of which was elongated in a direction west-southwest, adjoined each other and virtually constituted a syncline sepa- rated from the Sacramento Valley by a rather prominent anti- cline. Perhaps my meaning may be clearer if I state that the four Cretaceous remnants are separated from each other by tracts of metamorphic rock which rise about 2000 feet above the deepest portions of the basins, but that the ridge of meta- morphic rocks which separates them from the Cretaceous in the Sacramento Valley is much higher. The average altitude of the bottom of the Cretaceous in the center of each basin is about 2500 feet. The ridge which separates them from the Sacramento Valley rises from an alti- tude of about 4000 feet at Harrison Gulch to over 7000 feet 36 C0. H. Hershey— Cretaceous Outliers in California. in Bully Choop peak. On the south side of this range the Cretaceous strata dip away at an angle about the same as the general slope of the mountain, and Cretaceous remnants occur at a considerable height on its flank. Indeed, Cretaceous peb- bles and the gold derived from the basal conglomerate are widely scattered over the slope and indicate that Cretaceous strata in place have but lately disappeared from it. Near Harrison Gulch and at Good’s Pass, where the ridge is lowest, the Cretaceous strata reach to the very summit and curve over its top. A careful reconstruction of the plane of the base of the Cretaceous upon data furnished by the basins on the north of the ridge and the Cretaceous border on its southern slope shows that the summit and slopes of this range must corre- spond roughly with the Cretaceous base-level upon which, after submergence, the Horsetown was deposited. It is the Cretaceous base-level brought to light by erosion. This base- level was deformed near the close of the Cretaceous to just about the same extent as is the present surface. The north- east-southwest range of which Bully Choop is the principal peak is, in a certain sense, a strnetural range although its present topographic prominence is due entirely to erosion. It almost exactly coincides in position and form with a post-Chico range. The most remarkable thing about it is that this post- Chico mountain range was thrown up almost at right angles to the strike of the metamorphic formations forming its core and, hence, to the post-Jurassic mountain system. If the post- Chico Bully Choop range rose rapidly enough so that its sum- mit was not materially reduced by erosion during the move- ment, at its completion it was a ridge with a base on the average 12 miles wide and rising in its highest peak over 7,000 feet above the lowlands on the south and 4500 feet above the deepest basin on the north. It became the main drainage divide and has continued so to the present. We do not know whether the same sharp deformation of the surface in post-Chico time persisted over the entire Klamath region, but there are evidences that it did. Wherever the Cretaceous strata are found on the borders of the Klamath region, they are tilted at a considerable angle. On the north- eastern flank of the mountains, in Shasta Valley, in the Sis- — kiyou Mountains and in the Rogue River Valley in Oregon, the Cretaceous strata rest upon the metamorphic formations | with their original contact, but are tilted toward the northeast at a high angle, in a few places nearly vertical. There isa general rise of the Klamath region toward the northeast and the highest portion of the upland occurs on the immediate border, just beyond which the surface abruptly falls away to C. H. Hershey—Cretaceous Outliers in California. 37 the deep broad basin on the floor of which Mt. Shasta and the Cascade range have been built up. The phenomena are sim- ilar to those which characterize the Sierra Nevada region with its short steep slope on the east and.a long gentle slope on the west, and suggest that the northeastern face of the Klamath Mountains marks the line of a great fault; but the relation between the steeply inclined Cretaceous strata and the older rocks shows that the structure is that of a sharp monocline rather than a fault. The Sierra Costa Mountains rise abruptly above a supposed Cretaceous remnant near Weaverville and on the northeast they are terminated by the sharp monocline above-mentioned. They must have been one of the abnormally elevated portions of the post-Chico mountain system. Berkeley, California. 38 O. C. Farrington—Action of Copper Art. IX. — The Action of Copper Sulphate upon Iron Meteorites ; by O. C. FARRINGTON. In 1852 Wohler* announced the discovery that some iron meteorites, irrespective of their nickel content or structure, are passive to neutral solutions of copper sulphate, i. e., they do not reduce copper from such a solution. This passivity he stated could be overcome by introducing a piece of ordinary iron into the solution or by adding a few drops of acid. No data were given as to temperature, length of time allowed for deposition or the strength of the solution. The following meteorites were reported by him to be passive: Bemdego, Bohumilitz, Braunau, Cape of Good Hope, Green County (undoubtedly Babb’s Mill), Obernkirchen, the Pallas Iron, Red River (probably Cross Timbers), Schwetz, Toluca, and the terrestrial iron of Greenland. A number of other mete- orites which need not here be enumerated he reported at the same time as “active,” i. e., they reduced copper from the copper sulphate solution ; while those of a third class were designated as “intermediate,” i. e., they were nearly passive, but after remaining some length of time in the solution brought about a slow reduction of copper. That the passivity was a property of the entire mass of the meteorite seemed to be proved by the fact that when the surface of the meteorite had been made active and the coating of copper was removed by filing, it would again behave passive. Since the publication of Wohler’s article several other investigators of iron meteorites have tested their behavior toward copper sulphate with the result usually of finding them active, but the following, as listed by Cohen,t have been reported passive: Toluca by Krantz, Knoxville by Smith, Misteca by Bergemann, Octibbeha County by Taylor, Ohaba by Bukeiégen (this is a stone), Charcas by Meunier and Lexington Co. by Shepard. Two of these, however, were reported by other observers to be active, viz: Toluca by Pugh, Jordan and Taylor, and Charcas by Daubrée. The observers later than Wohler also failed to give details regarding the conditions © of their experiments. Wicke and Wohler state that the Obernkirchen meteorite, after remaining a day, reduced no copper from its salts.t Smith states that Knoxville is passive with reference to the action of sulphate of copper, but when immersed in a solution of the latter and allowed to remain several hours the copper deposits itself in spots on the surface * Poggendorff’s Annalen 1852, vol. Ixxxv, pp. 448-9. + Meteoritenkunde, Heft 1, p. 68. ¢t Ann. d. Chem. u. Pharm., 1864, vol. cxxix,, p. 123. EE a a Sulphate upon Iron Meteorites. 39 of the iron.* Meunier states that the section of Charcas was washed in alcohol and ether to remove grease and upon it a drop of solution of sulphate of copper was placed. At the end of some hours the drop had evaporated, leaving crystals of the salt but no copper.t Viewed simply as a matter of reasoning, it would seem quite impossible, with our present knowledge, to account for a passive behavior of meteorites independent of their nickel con- tent. As is probably generally known, nickel is less active to copper sulphate than iron, and it might be expected that the activity of alloys of iron and nickel would decrease in propor- tion as the percentage of nickel increased. But that some individuals of the same alloy (for iron meteorites are practically alloys of iron and nickel) should be entirely passive while others were normally active would be quite extraordinary. Wohler’s conclusion was that all iron meteorites were probably in their original state passive, but that throngh local terrestrial influences and the passage of time, some had since their arrival upon the earth become active. Meunier expressed the opinion that a peculiar molecular structure may be indicated by the passivity.t In view of the lack of details regarding the experi- ments upon which Wohler based his conelusions and the results he obtained, it seemed to me desirable to reinvestigate the matter to some extent. Of the meteorites listed above as passive, there are to be found in the collection of the Field Columbian Museum, specimens weighing from 10 to 1100 grams each, of the fol- lowing: Babb’s Mill, Bemdego, Braunau, Bohumilitz, Cape of Good Hope, Chareas, Cross Timbers, Knoxville, Lexington Co., Misteca, Pallas Iron, Toluca and the native iron of Green- land. These therefore were available for investigation. In order to test their activity each section was in turn immersed in a solution of 200 grams of Baker & Adamson’s C. P. copper sulphate to a liter of distilled water. The temperature of this solution was about that of the room, or 18° C. In this test every meteorite gave an active reaction. * ey Lennoxvile. 8 \ ix] Paleozorw Scale. = ° to milés \ A Part of the Eastern Townships of the Province of Quebec. and that between the vicinity of Quebec city and the United States boundary line as the Notre Dame Hills. The district lying within the Notre Dame hills is commonly designated as the “ Eastern Townships,” the geological structure of which has furnished the theme of imuch well-known discussion during the past forty years. This has been chiefly connected with the question of the Quebec Group.* * “Geology of Canada,” 1863, pp. 225-297, by Sir W. E. Logan. **The Quebec Group in Geology,” Transactions of the Royal Society of Canada, vol. I, 1882, by A. R. C. Selwyn. ““Notes on the Microscopic Structure of Some Rocks of the Quebec Group.” Ann. Rept. Geological Survey of Canada, for 1880-1-2, by F. W. Adams. ‘*“The Quebec Group.” Appendix A to Harrington’s Life of Sir W. HE. Logan, by Sir J. W. Dawson, 1883. Reports of the Geological Survey of Canada for the years 1886, J; 1887-8, K ; 1894, J, by R. W. Ells. 44. Dresser—Contribution to the Geology of Quebec. As originally defined by Logan and Billings, the Quebec ~ Group embraced all the rocks of the Eastern Townships that are essential to the present investigation, and all were then regarded as of sedimentary origin. Subsequently, however, Hunt, on stratigraphical grounds, and Selwyn on stratigraphi- cal and lithological evidences, distinguished certain older measures, which were referred by the latter to the early Cam- brian and pre-Cambrian ages. The amplification of the views has been fully carried out by Ells in the reports of the geo- logical survey of Canada for the years 1886 and 1894. The only lithological changes embodied in these re- ports are in the recognition of the eruptive origin of the serpentines and the diorites, diabases, porphyrites and granites generally associated with them. These had been previously regarded as metamorphosed sediments. The silicates of magnesia were correlated with its carbonates, where dolomite occurred in the vicinity of the serpentine belt, and even in 1886, Dr. Selwyn, who had been the first to recognize the igneous origin of the serpentines, in a footnote appended to Dr. Ell’s report, maintains that the hornblende granites are probably products of metamorphism in situ and not true intrusives through the serpentine, as the latter writer correctly considers them to be. In respect to age, the serpentines and certain of the clasties were referred to the early Cambrian and the other eruptions to middle or late Silurian time, while three belts of supposed sedimentary rocks, running approximately parallel to the north- easterly trend of the Appalachians were classed as pre-Cam- brian. One of these appears for only a relatively short dis- tance along the boundary line between the province of Quebec and the State of Maine. The second crosses the St. Francis river between the city of Sherbrooke and the vil- lage of Lennoxville. This may be known as the Ascot or Stoke Mountain belt, while the third, which crosses the St. Francis river a little way north of the town of Richmond, twenty-five miles northwest of the second, is generally designated as the Sutton Mountain belt. The structure of these bands, especially of the last mentioned, was long a crucial point in the Quebec group controversy, they being interpreted as syn-. clines by the earlier investigators, and as anticlines by the latter. PETROGRAPHY.—Recent petrographical investigations by the writer have, however, shown that both the second and third of these pre-Cambrian belts consist largely, and in places entirely, of altered volcanicrocks. These are so highly altered and consequently so much disguised, that they have : Dresser— Contribution to the Geology of Quebec. 45 been hitherto mistaken for sedimentaries, and have been accordingly treated on that assumption in all the stratigraphi- eal discussions regarding them. (a) Inthe Stoke Mountain belt the principal rocks exam- ined were taken from the township of Ascot, on the west side of the St. Francis river, between Sherbrooke and Lennox- ville. Others were taken from various points to the south- eastward on the upper Belvidere road and from the vicinity of the Suffield, Sherbrooke and Clark copper mines. The rocks, which are generally fine in texture, are of various shades of green and gray in color, and many are in advanced stages of metamorphism. In the thin section, however, the microstructure remains sufficiently distinct to clearly establish the igneous origin of practically all of these rocks, and even to identify the specific characters of several on the merely preliminary examination of them that has yet been made. Quarte-porphyry forms the hanging wall of the Silver Star mine at Suffield. It is of light gray in color, and from the prominence given the quartz phenocrysts by the bleaching of the base of the rock on weathered surfaces, it has been com- monly regarded as a species of sandstone. By the aid of the microscope the structure is found to be that typical of an effusive rock. A very finely crystalline base holds phenocrysts of quartz, which show in basal sections an uniaxial cross and positive sign ; and also of feldspar, which extinguished in several cases with its principal axes parallel to the planes of the crossed nicols and hence is ortho- clase. A few feldspars are polysyntheticallv twinned and accordingly are plagioclase. Their extinction angles are small. Small rod-like individuals of colorless mica arranged in lines are presumably of secondary origin. They often occur within, or in association with, irregular areas of a rhombohedral carbonate, apparently dolomite. Granite-porphyry occurs near Lennoxville on the line of the Canadian Pacific Railway. It differs from the quartz-porphyry chiefly in the more advanced character of its crystallization, both quartz and feldspar being distinguishable in the ground- mass. A little chlorite, pyrite, brown iron oxide, and color- less mica are also present. An incipient cataclastic structure is beautifully shown in both of these rocks. The quartz-pheno- crysts are sometimes reduced to mosaics of quartz grains, or at others are crossed by lines of crushed material, while the erystals on either side of the lines remain unchanged or show undulatory extinction. Being the largest single masses and of the most brittle material, the quartzes thus appear in every case to be the first constituents to show the effects of purely dynamic metamorphism. A much altered rock form- 46 Dresser—Contribution to the Geology of Quebec. ing the hanging wall of the Clark mine was probably closely allied to the quartz-porphyry in its original composition. It rather closely resembles a specimen of “sheared felsite ” from the Gettysburg Railway, south of Clermont House, Monterey, Pennsylvania, seen in the petrographical collection of McGill University.* A greenish gray fine-textured massive rock is of large extent, especially in the southern part of this belt. In the thin section quartz is found in broken phenocrysts and also in smaller grains, presumably primary, in the rather fine holo- crystalline groundmass. Under high power (x220) feldspar appears in the groundmass in small lath-shaped individuals which extinguish at low angles with the principal axes. Epi dote and chlorite are abundant representatives of primary bisilicates. The rock would have originally been abont of the character of a quartz porphyrite. A large part of the central and southern portions of this belt in the township of Ascot is occupied by a highly foliated rock of green color and massive appearance. Under the microscope a little feldspar is found in an aggregate of color- less hornblende, chlorite, epidote, dolomite and sericite, all of which are secondary constituents. This rock agrees essentially with the sheared greenstone from Jack’s Mountain tunnel, near Monterey, Pennsylvania, as seen in the McGill University collection. A similar but more dolomitized rock occurs in various parts of the belt, one occurrence of which is-mapped as igneous on the map to accompany the Annual Report of the Geological Sur- vey of Canada for 1886. These rocks, though probably of several different ages of eruption, are generally much metamorphosed. But cutting them thereare dikes of camptonite and olivine diabase, which are quite undisturbed in position and comparatively little altered in mineralogical composition. They also cut the Lower Tren- ton strata along the edges of the belt, while these overlie the other igneous rocks of the region. Whence it appears that the Stoke Mountain, or Ascot belt, has been the scene of volcanic activity at various periods through a long range of time, from pre-Cambrian to post-Trenton. 1D Ay Dermochelys, 100 43 ao A387) “160%, 209 7: 86 23 Eretmochelys, 100 53 44 49 Se) A258)... 105 44. 12 Archelon, 100 54 51 — — — 21 Toxochelys, 100 58 50 51 73 100 = 104 de AO ery eh Chelydra, 100 52 53 50 72 73 a) 50 (small) Acichelys (=Eurysternum), 100 S57 51 i oO or mse 63 66 d1 ti Inspection of the above table shows: 1. Strongly marked radial and ulnar decrease in length. 2. Greater or less elongation of the radius as compared with the ulna. 3. Nearly static length of the first finger in the Chelonidan forms, with sharp increase in Dermochelys. | 4. Persistent increase in the length of fingers 2-4. 5, More or less variable tendency to increase in length of the fifth finger. 6. Great pisiform increase, which began relatively early. 98 G. R. Wieland—On Marine Turtles. Measurements of Toxochelys latiremis. (All are from the same individual.) The Skull. M. Extreme length from beak to extremity of the supra- occipital process, which is complete_-__-__-.----.----- 152 Length from beak to occipital condyle ___.._..-.-......) “14 Exiteme width -~.. 2... 8. See ee ee ee Width between articular surface of quadrates ___-_--...- 078 Length from beak to anterior border of internal nares __-- 025 Extreme length of ramus of lower jaw.---.---.-------.. ‘ll The Cervicals. Leneth of ist cervical centrum (2. +=. ee 6 014 Length of 2d = wens etc .oh 2G Ge ee Length of 3d Re PES \ hen So hoo yd Soe Se ae — Length of 4th ‘“ Ase) Chasis oe oe Se Ce 033 Length of 5th “ Fi Nit De ee See eee — Length of 6th “ ST ety oe et eae ae St oe Length of 7th “ ett tek ee ee 031 Length of 8th “ Bore) Be Disk tees ae "03 Estimated total length of the eight cervicals _.-.-------- 226 Length of Ist dorsal centrum £2 /°_.. 22-22 22352 ee ee The Humerus. M. Greatest lenoth .__-.. = @. £222 85 135 Depression of radial crest beneath proximal extremity.-.- °02 Distance of ectepicondylar groove from distal anterior perder 202 23. .005 Greatest length of the other elements of the front flipper : Padi sk Pe ee ee ‘075 | Metacarpale, TIT __-___ S3ga8 pte eee 066 — $ TV ee 055 iupermediom 2. 22 018 | <7 YA ee 037 Diaare ©. 22-2. a Ae ee 017 }Phalanx, I-12." _) >= eemuemie 222 So S50 Mas O15 60 Teo. (claw) 2-00 ee Warpale) eo be sii). P83 ae sep DSA aE Ris | Everett "02 aire hae. Tesi 015, Ke top Eas Sek ee 019 77 (Sac. Dagar baths Repti 013 | “<* Ii-3 (claw). 2-025 "OS ee i Oe Ra eae 013) Phalanx TEi—t 2). ee ‘034 a Wig ett Fd 2 ‘O11. cI }i-9 '._-..) eee Pipi fee oS OES EY 1. ee * +036 Metacarpale, 1 ....---. "023 | MN ole eee 031 ae 1, Sipe dai Saag ‘035 Total lene ch first, finger __._ 2. 2. eee ee "65 “- ” second finger Bebe ain = = pep ee Ec, ee Estimated lensth, third finger... . coe 2s “13 3: fourth finger a no 2c ny eo are a oe SST eiet Rewer. 62. | 2! ole 09 ~~: G. R. Wieland—On Marine Turtles. | 99 Il. The Front Flipper of Archelon ischyros. In my first description of the gigantic turtle skeleton from the Fort Pierre Cretaceous of South Dakota which constitutes the type of Archelon ischyros,* I figured, in addition to other skeletal parts, the humerus, radius, ulna, femur, tibia, and fibula, and mentioned the fact that a number of carpals and tarsals with several phalanges were also present. This was practically the first contribution presenting the main features in the limb organization of the [Protostegine]. Hitherto our knowledge of the flippers of these great turtles had been lim- ited solely to that given in Cope’s original description of the first member of the group discovered, Protostega gigas.+ In this form the humerus was described and figured together with the radius. and ulna, although the latter were then supposed to be “ metapodials”’ rather than bones of the forearm. As there was at the time of my first publication an absolute dearth of information concerning the carpal and tarsal structure in marine turtles from the American Cretaceous, not one hav- ing been described, the fear that | might make some serious error prevented my publishing the restoration of the carpus which I then made, the various elements having been found only partly in position. | Now, however, Professor Willistont has just described the hind flipper of Protostega, and this enables me by exclusion to determine with a reasonable assurance of correctness that the elements [ originally assigned to the carpus in my study of the closely related Archelon truly belong there. Iam hence able to add some further facts concerning the skeletal organization and systematic position of these highly interesting Testu- dinates. The partial restoration of the left fore flipper shown in figure 2 is based on the radius and ulna, with what are consid- ered to be all of the carpals but two, together with the first and fifth metacarpals. Several phalanges are present, but as finger proportions may vary markedly it is not deemed advis- able to attempt a complete restoration. The value to be attached to this preliminary restoration is provisional, as follows : (a) The radius and ulna are simply drawn in a generalized position, but their orientation is based on that found in a sec- ond specimen where these bones were in an approximately normal position with respect to the humerus, only. *G. R. Wieland.—A New Gigantic Cryptodire Testudinate from the Fort Pierre Cretaceous of South Dakota. This Journal, fourth series, vol. ii, December 1896. + Loe. cit. ¢S. W. Williston.—On the Hind Limb of Protostega. This Journal, fourth series, vol. xiii, April, 1902. 100 G. R. Wieland—On Marine Turtles. (b) Carpalia 3-5 were found in succession, and are doubt- less correctly placed. (c) There is little doubt but that the intermedium and ulnare are correctly determined, but their precise orientation is not so certain. Thus it may be that the intermedium should be rotated in a vertical are of 90°. This, however, would not greatly alter its general contact outline, as it is a very robust and much rounded instead of flattened bone. (d) Since metacarpal I and the pisiform are beautifully preserved, both as to form and surface markings, the possible remaining margin of error as to the identity of the several parts is shght. Figure 2. Archelon ischyros Wieland. Partial restoration of left front flipper, xt R, radius; U, ulna; P, pisiform ; I, carpale 1; V, carpale 5. Description. Since the peculiarities of the Awmerus have been quite fully dealt with in my article on the Evolution of the Testudinate Humerus, this bone need not be further men- tioned now, except to recall the fact that it resembles the humerus of Dermochelys more closely than any other, although differing in some very essential features. The radius is only slightly longer than the ulna. Proxi-- mally it is triangular, and distally, rather elliptical in trans- verse section. The most marked characteristic whatsoever is the strong proximal bow, which recalls the lesser proximal bow seen in the radius of Dermochelys. Otherwise this form has a rounder, heavier head. The proximal articular face is only slightly concave, its general outline being that of an isos- celes triangle, with the base in contact with the inner face of the ulna. G. R. Wieland—On Marine Turtles. 101 The wlna@ is short and massive. The proximal articular sur- face is slightly crescentic in general ontline, and somewhat concave except for an oblique, low, saddle-shaped ridge which divides this face into subequal areas, the larger facing towards the radius. The distal articular surface is moderately convex antero-posteriorly, and rather flat in the dorso-ventral direc- tion. The bone has a distinct broad and shallow grooving on. the proximal ventral, and on the distal anterior side, marking the proximal and distal contact with the radius and producing the effect of a marked twist corresponding to the high angle between the general trend of the proximal and distal articular faces. Asin the case of the humerus and radius, there is a certain correspondence with Dermochelys, but the ulna of the latter is more rounded. | The intermedium is much rounded and very robust. The ulnare is suboval in external outline, with the proximal edge much the thicker. The pzszform is very large, of subcrescen- tic outline, thick, and quite flat, but with a raised border on both faces. The carpalia and metacarpals present have more the appear- ance seen in the Chelonine than in Dermochelys, in which respect there is in fact a wide difference, the pronouncedly marine appearance of the rounded subcylindrical and flat-ended metacarpal and phalangal bones of the latter being quite absent. General Resemblances. Inso far as now known, the manus and pes of Protostega and Archelon resemble those of Dermo- chelys rather more than any other form. Briefly pointed out, the more marked similarities of the manus are, the approxi- mately equal length of the radius and ulna, the heavy proximal bow of the radius, the earpal organization with the centrale excluded from contact with carpale 1, and an enormous pisi- form set high up near the ulna, and mainly on the ulnare. The point of most importance and necessarily of the greatest difficulty to settle with complete satisfaction is as to the assumed contact of the centrale with carpale I. Professor Williston has, I think, omitted one of the tarsalia from his restoration of the hind limb of Protostega, so that there is likewise an even closer general correspondence between the hind limbs of these several forms than he suggests. The diminution of the fifth finger of the hind flipper, as he shows, to a single metatarsal is, I suppose, not to be regarded of as much importance as any reorganization of the carpalia or tarsalia (loc. cit.). 102 EDRO Fg Wasa on Marine Turtles. Measurements of Archelon ischyros. (From the type specimen.) The Radius. Meters. Ui) Mite perenne iy AeA. peed De aMpm yar earne 35 Proximal diameters: 2... J. oo ke ele. . Ree Least. diameters.of shaft-.o2-...2 002-1. .:.._.. "05 / meee DDistaleeiametens:= 0 see e ee A kg ee "049 and ‘114 The Ulna. Hength’_ os 242. SL ee Ss So ee ee "33 Greatest and least - pr ‘oximal diameters ......-.--- 093 and *14 | < “diameters of shafti2: oo 22) O64 | « Geo a eittr* Guistall: diamiebers<2 os. Thee eres ‘088 and 138 ; Measurements of carpals and metacarpals, viewed from dorsal surfaces : Greatest length. Greatest width. Entetmedinancte. ete) te °8 shet Wibaater S50 dew Gast. Pe he “Th 08 Psi. 221 be Boe aie ae eee 14 12 Centrale. fo. is. ee Ye "048 ‘06 Canpalecg hast. 1.) Seer es Cooke 04 07 ce Tk SP Tas ict es kT Bete a ee se sy I Aegean amet SAE a Ey tia pe "06 "056 ue EV: 2 lier OE yi ein aa ened ‘068 ‘068 ne i GCA, MAES MR acl eRe ‘06 072 Metacarpale 1S OS Pees ‘09 "10 imal ee hc Ra A Sle "156 °056 The extreme length of the accompanying humerus is °65 meters. Ill. Zhe Cervicals of Toxochelys and Archelon. (See Measurements, p. 98.) The cervical formula has not hitherto been given for any of the Cretaceous marine turtles, so far as the writer is aware, our knowledge having been restricted to scattering or isolated vertebre. I may hence give the formula for Toxochelys, and will show that that of Avehelon may also be determined as quite similar, smce we know the vertebrae most susceptible of change, the last three. In the Yale specimen of Zoxochelys (see Measurements), the first, second, fourth, sixth, seventh, and eighth cervical vertebree are present. The nature of the other two, the third and the fifth, of course follows, as included arbitrarily in the subjoined table, in which are given the formule for the present forms and several others presenting interesting or im- pue ‘A[101109s0d xeauoo A[qnop puv ‘ATLoLIeyUR eAvoUOD A[Quop=uRe,tAoIq-oO]~MoIg ‘ eAVOTIOD-a[(Nep=URITOD | xeAMoo-e]q(nop=ure4tsO uveytho -oy1AOTG GE TOOT -04th—) bi) 9) bp) 9) uUBIpODOyILD, xel duo ‘wafiuds LAUT, ae ) uvayts00[0D ? orddiydy uveytsyy xaduiog ‘snUDYLMaWwng srMawoopog IITA ) Le) ”” ? “Pe uBeyAD0][AD uve4y1Ad xe[dutog ‘(purry) sasuar -Unaspbvpvyyy shvoyoouwmhay ITA weet A01q, -OgaAOLg WeTTPOOT -o[oorg uveyt£01q “OT@) weayTADOTCOL we94akO ? UWBITA904AALD xo[dutog ‘snucaydlijod opnysa], IA uva4ztho -O[OoIg weoqaAOLG, -O[ MOTT uvoypthorq Of) wWRaytADOTHOHD uraytd—a ) URT[CI0}.LAL) xotdurog *punuaduas paphjeyO A uReyLAo -O[OOTg | twRaytAdIq AYR] | uvdye[dopap uvoytAd0[a~—) uvaytdD i] WRI[HOI0yLAD, xeTduton “DPDIVQUL shpayooujany AI | | ueeytho -O[Md0Tg | uveytA01q, -O[))| 1) uvoayprho0]e09 uvoythp 2) UBIToIOyI AEA xo[dutog *“ad0D1LN09 shjayoouldad TE uvoythoojaoQ | ureyt£o0p~ag uvaythy uvoqiho 9?) ) uvIpoooytdg | uvije00,1h9 xo[dutog xo{durop *s7Ua dn) ‘souliyose ShpAYIOXOT, U0)AYIN II E ?) ? Pr) . “AT[VLOZVT Yoou oy} Surzoerjor FO FIQVY oY} JO 4[NSet oyy sv ssey}qnop ‘sparq Jo osoy} sv podvys-e[pprs ATjouLsSIp sv oyinb ore spumauoopog JO s[eolAteo Y4XIS—paAlyy ey, * ‘shjoyouyanigy UL se wveytdorqAqeid soyovordde shjyayoowuag Jo } ‘ON “eIZUed pezyeutuLte} A[ZVy Lo ‘xesuod-e[qnop ‘eAvouod-o[qnop oyut dofeasp AT[wngov you op ynq, *peorq aie s/izayooxoy, JO S[VOLATEO 4ST OUT, ; ‘eg, “d ‘6681 “Qsnony 10j [eUIMOL sTyy veg 9 9 ? V "[ROTALOD 104 G. R. Wieland—On Marine Turtles. portant comparisons. All taken together display the great variations seen in particular in the last five Testudinate cervi- cals. I may explain that I have introduced a modified nomen- clature I proposed in this Journal for August, 1899, p. 163, since the ordinary and incomplete terminology does not ade- quately express the complicated forms seen in Testudinate cervicals. The cervicals of Zoxochelys are distinctly intermediate in character between those of Chelydra and the Chelonide, being most like the former. The ends of the sixth, seventh and eighth broaden, but there are no distinctly biconcave, bicon- vex, or flat terminations, these vertebra. still being proccelons (ceelocyrtean). Their centra have strongly marked elongate and thin or blade-like keels, quite similar to those of the sixth and seventh, but not the eighth centrum, of Chelydra. The total length falls far short of that seen in the Chelydride. In Archelon, the sixth, seventh and eighth cervicals were found in place in the type specimen, as well as several others. All are characteristically proccelous (=ccelocyrtean), and none have their anterior ends markedly broadened as in Zoxochelys. They are also relatively much shorter than in Zoxochelys, and very robust (loc. cit.). I have estimated the cervicals of the type specimen of Arvchelon as having a length of -72™. The cranial length must be about the same. But in Toxochelys the total length of the cervicals is about one and a half times, and in Chelydra twice that of the cranium. We cannot doubt: that the fourth cervical was biconvex (Cyrtean), since it is so in all known marine Testudinates. The vertebrae of Archelon are on the whole rather more primitive than in any other marine turtle, and it is certainly very interesting that there should be a closer agreement with Zoxochelys than any other form. IV. Béaring of the Foregoing Data, and Classification. A phylogenetic classification of the marine Testudinates will still be held more or less difficult to deduce, according to the view that is taken of the much debated descent of Dermochelys. In weighing the evidence at present available, however, it needs to be borne in mind that the wide distribution of the turtles in latitude and time necessitates the consideration of slighter differences than in the case of more variant forms. While this must finally be a great advantage, it is a fact that at present brings home to us with force our imperfect, but happily rapidly increasing, knowledge of the- fossil record. Again, there is a constant danger that in such a case one may regard evolution as having taken a far simpler course than has a Z a : ‘ " G. R. Wieland—On Marine Turtles. 105 really been the fact. It would appear that several hypotheses yet require consideration, as follows: (1) All the known marine Testudinates may be the de- scendants of a single littoral species. (2) Dermochelys on the one hand, and all the other marine forms on the other hand, may have descended from two dif- ferent littoral species of the same genus, or from different genera. (3) Dermochelys, Toxochelys, Protostega, and the living Chelonide may represent the descendants of four genera of the same, or closely allied families. (4) Dermochelys is of ancient descent, and stands phyleti- eally and morphologically opposed to all other Testudinates. Doubtless the final truth will be found to lie somewhere be- tween the first and last extremes. Certainly it is. difficult to overthrow the conclusion as to the general fact of descent as thus expressed and as defended with such signal ability by Baur :* “Dartiber aber ist kein Zweifel dass Dermochelys und Psephophorous keine urspiinglichen Formen sind, sondern dass sie von wahren ‘Thecophoren’® und zwar yon den ‘Pinnaten’ abstammen, um mich hier dieses Ausdrucks zu bedienen.” Dollo,t originally a strenuous opponent of this view, has recently adopted it. Taking up the question in further detail, he holds Dermochelys to be descended from a pelagic Theco- phore with an extremely reduced carapace and plastron, but the descendant of a littoral Thecophore with a fully developed carapace, and a plastron without fontanelles. And this eminent scientist has proposed the ingenious hypothesis that such a Thecophore again acquired littoral habits, resulting in the formation of a heavy mosaic carapace, which, with a second resumption of pelagic habits, again began to disappear, and is still in process of reduction. The persistence of the nuchal is held to be due to its value as an attachment for the nuchal ligaments. However involved such an_ evolutionary process may appear, it is skilfully presented, and has much in its favor. On the other hand, Hay{ has presented at considerable length facts favoring a very early origin of the Dermochelan line. * G. Baur.—Biologisches Centralblatt, Band ix, 1889, p. 191 (Erlangen). + L. Dollo.—Sur Vorigine de la Tortue Luth (Dermochelys coriacece). Ex- aay Bull. Soc. roy. des Sciences Med. et Nat. de Bruxelles, Seance 4 fevrier, tO. P. Hay.—On Protostega, the Systematic Position of Dermochelys, and the Morphogeny of the Chelonian Carapace and Plastron. American Nat- uralist (Boston), Dec. 1898. 106 G. R. Wieland—On Marine Turtles. _ Presumably the evidence in favor of Baur’s view is increas- ing. The writer so regards it. The fact that the cervicals of Toxochelys and Archelon agree in general, and at the same time differ most widely from the cervicals of Dermochelys and of the Chelonine, is, however, rather unexpected. Did the vertebrae of these Cretaceous forms tend to simplify, or has there been a more or less remote homoplastic parallelism in the course of complication in the case of the sixth, seventh and eighth vertebree of the modern sea turtles, and such widely different forms, for instance, as the Testudinide ? The question at once arises, what is to be regarded as a very primitive Testudinate cervical, and what was the form in the species, genus, or group which made its way into the sea and gave rise to the marine group? We may most reasonably suggest as avery primitive cervical type, that of a turtle like the Plenrodiran Arymnochelys, in which there is a well-nigh complete agreement with the modern Crocodilia, the second, and not the fourth, centrum being biconvex. And we assume that some descendant of such a primitive type, with double convexity moved back to the fourth cervical centrum, the fifth-eighth centra remaining simply proccelous, stood in some common ancestral relationship to the sea turtles and most other existing Cryptodirans. It would at present, therefore, seem that even since the sea turtles split off from their littoral an- cestry there has been a certain parallelism in the secondary cervical modifications undergone by them and the most nearly related land forms. This may hence prove, once we know the record more completely, to be another example of the fact that a course of evolution and change once established in a persistent group, may long continue, after the invasion of wholly new environments. There is in biologic, as in physical evolu- tion, inertia. As to the carpus of Avchelon. It will certainly be very interesting if my surmise that there is no union between ear- pale 1 and the centrale should prove correct. This, although to be regarded as a secondarily acquired character, would in- deed go far toward narrowing the gap between the extreme ends of the marine group. I may point out that the greatly accentuated bow of the radius of Archelon would make it probable, even in the absence of more direct evidence, that there was present some marked change in the order of the carpals. | Systematic Position of Archelon. While the data given in the preceding notes go far towards showing that Protostega and Archelon present more osteological resemblances to Der- mochelys than any other turtles whatsoever, living or extinct, their structure is essentially that of the Chelonidae, of which G. R. Wieland—On Marine Turtles. 107 they may best be regarded as a subfamily, the Protostegine. Moreover, these Dermochelan resemblances are only what we might well expect in Cretaceous turtles. There are likewise, as we see, certain Chelydran resemblances in the general type of skull, just as there are also Chelydran resemblances in Ti oaochelys. Weare simply following convergent lines back sufficiently far to somewhat accentuate general relationships. Position of Toxochelys. The fore flipper and cervicals of Toxochelys present some additional Chelydroid characters to those of the cranium and lower jaw, as already pointed out by Cope and Hay. TZoxochelys hence proves: to be one of the most interesting of turtles. Like Pvotostega and Archelon, it points with more or less distinctness toward a Chelydra-like ancestry. Baur has said that this genus should be placed in a distinct family, and in this has been followed by Hay and Case. But I think that Zozochelys may more conveniently be considered as representing a subfamily of the Chelonide, cer- tainly if of common ancestry. V. Provisional classification of the marine Testudinates. CHELONIOIDEA (Baur). (Superfamily of the Cryptodira.) A parieto-squamosal arch; palatine foramen and free nasals sometimes present (Desmatochelydinz); fourth cervical bicon- vex, with the centra of the sixth, seventh, and eighth usually greatly moditied. I. Dermochelydide. No descending parietal processes; no palatine foramen ; other cranial and limb characters not remote from those of the Chelonidz ; carapace represented by the nuchal only, and body enveloped 1 in a leather y hide with an osteodermal mosaic ; no claws. Genera: Dermochelys, Psephophorous, Eosphar gis. ‘Il. Chelonide. Skull with descending processes of parietals, so far as known ; palatine foramen sometimes present ; vomero-premax- illar union often, but not constantly present ; a normal, though often much reduced, carapace and plastron : nuchal with or without process on under side ; claws, one or two. 1. Protostegine.—No free nasals; no palatine foramina ; obturator foramen small and enclosed by ischiopubic contact on median line, as in many land forms. Genera: Protostega and Archelon ; Protosphargis? Pseu- dosphargis ? 108 G. I. Wieland—On Marine Turtles. 2. ‘Toxochelydine.— No free nasals; palatine foramen, pterygoids, and lower jaw distinctly Chelydra-like ; two strong claws. Genera: Toxochelys, Porthochelys, Cynocercus(?), all of the Niobrara Cretaceous of Kansas, also Veptunochelys from the Cretaceous of Mississippi. 3. Desmatochelydine.—Free nasals; distinct palatine fora- mina (except Lhinochelys?). | Genera: Desmatochelys, Rhinochelys, Atlantochelys. 4. Chelonine.—No free nasals; no palatine foramina ; vomero-premaxillar union often, but not constantly present ; obturator foramen presumably not enclosed as in Archelon in any member of the group; claws, one or two. Genera: Osteopygis, Allopleuron, Lytoloma, Argillochelys, Eretmochelys, Chelone, Colpochelys, Thatassochelys. * ; a9 * vis * 9 ftesume.—In the foregoing notes the following additions to the osteology of the marine Testudinates have been made :— The elements and organization of the front flipper of Zozo- chlys The-main elements of the wrist region of the front flipper of reer ischyros. (These are described from the type of the genus and species. The writer, in his first announcements f the discovery of this gigantic turtle, figured and described the accompanying humerus, with the radius and ulna, as well as the femur, tibia, and fibula,—this being the first instance in which all these limb bones were made known-in the case of any extinct. eure ‘Testudinate.) 3. Important measurements for the codrdination of various skeletal elements of Toxochelys and Archelon. 4. The deduction (with the exception of the secondary rear- rangements of the carpals) of the principal lines of change in the evolution of the fore flipper from the foot of some primitive swamp, or littoral, Chelydra-like turtle. 5. The cervical organization of Yoxochelys and Archelon, which is compared with that. of living turtles. 6. A classification of the marine turtles.—This has chiefly been made possible by the description during the last few years of large portions of the skeleton of Protostega and of Toxochelys, and especially by the discovery of Desmatochelys, Archelon, and Porthochelys. Yale Museum, New Haven, Conn. April, 1902. Se ee ee ee Whitehead— Magnetic Lifect of Electric Displacement. 109 Art. XV.—The Magnetic Lifect of Electric Displacement ; by Jonny B. Wuirrnran, JR. HistroricAL REVIEW. In the development of his theory of the electromagnetic field, Maxwell assumes that the phenomenon of polarization in a dielectric consists of an actual propagation or displacement of charge in the direction of the polarization ; that in the case of the charging of a condenser, for instance, this act of displace- ment is equivalent to a current at any instant equal to the rate of change of the surface charge on one of the plates, i. e. ae 4s q being the current density, K the specific inductive capacity and F the difference in potential per unit length, and that therefore the current is continuous throughout the circuit. He assumes further that the displacement current has the same magnetic effect as would be produced by a conduction current of density g= eek so that in the case of the condenser the 4 dt’ magnetic effect in the neighborhood, incident upon any change of charge, would be due to the combined influence of the cur- rent in the charging wires and the displacement current in the dielectric.* ‘It appears, therefore, that at the same time that a quantity Q of electricity is being transferred along the wire by the electromotive force from B towards A, so as to cross every section of the wire, the same quantity of electricity crosses every section of the dielectric from A towards B by reason of the electric displacement.”’ (Art. 60.)...... “The variations of the electric displacement evidently con- Ememievelectric currents.” -(Art.60.)...... “One of the chief peculiarities of this treatise is the doctrine which it asserts, that the true electric current C, that on which the electromagnetic phenomena depend, is not the same thing as K, the current of conduction, but that the time variation of D, the electric displacement, must be taken into account in estimating the total movement of electricity.” (Art. 610.) The remarkable consequences of Maxwell’s theory seem to justify his assumptions beyond all question. There need only be mentioned the finite velocity of propagation of electric and magnetic actions, this velocity being the same as that of light; the electromagnetic theory of light, which accounts for the results of experiment, practically without exception; the * Maxwell: Electricity and Magnetism, Art. 60, 75, 76, 111, 328-334, 608, 783, 791. Am, JOUR. a SERIES, VoL. XIV, No. 80.—Avaust, 1902. 110 Whitehead—Magnetic Effect of Electric Displacement. experiments of Hertz on electric waves showing them to be identical in behavior with light waves. The direct magnetic effect of the displacement current, however, has never been satisfactorily observed, if at all; published accounts of work in ~ this direction seem to be limited to those of Roéntgen, S. P. Thompson, Nicolaieff and Blondlot. . Léntgen.—The earliest attempt, apparently, was that of Rontgen in 1885.* He rotated a rubber disc between two stationary glass plates all in horizontal planes. The upper plate was coated with tin-foil which was grounded; the lower plate had on it a ring of tin-foil which was split along a diam- eter and the two halves oppositely charged. As the dise rotated there was a change in polarization at those portions of it passing over the opening in the tin-foil, and the resulting displacement current was in opposite directions at the two ends of this opening. Over the whole system and as close as possible to the upper plate, he suspended an astatic needle whose direction was along the line of the opening in the tin foil, and the line of suspension the continuation of that of the axis of the rotating disc. The length of the lower needle brought its ends to the center of the width of the tin-foil rings ; any magnetic effect of the displacement current would thus tend to deflect the astatic system. On commutating the charges on the rings the deflection read by a mirror and scale was never over 1°5™", and the needle was subject to an oscilla- tion of that amount due to disturbing influences. The ob- server, being ignorant of the direction of commutation, was supposed to take into account the motion already possessed by the needle in giving the direction of the resulting impulse. Rontgen states that after 1000 observations he acquired such practice as to be able to observe the proper direction nearly every time. The results of this work can hardly be considered conelu- sive. That little importance is to be credited to it is evidenced by the small notice it has attracted. The genuineness of the observed deflection is particularly to be questioned in view of the fact that the poles of the needle were not in proper posi- tion to experience the full magnetic force of the displacement current. Each pole was entirely above the plane of the sur- face of the dielectric, and it may well be questioned what is the distribution of the magnetic field beyond the terminating surface of an ‘open current.” Thompson.—In 1889 S. P. Thompsont wound an iron ring with many turns of fine wire and imbedded it in a block of paraftin having on two sides parallel to the plane of the ring * Rep. der Physik, No. 21, 1885, p. 521. + Proc. Roy. Soc., xlv, p. 892, 1889. Whitehead— Magnetic Effect of Electric Displacement. 111 metal coatings which were connected to an induction coil. The winding on the ring being connected to a telephone receiver, sounds were obtained on charge and discharge of the coil. Very slight conductivity in the paraftin would have caused this. Nicolaieff—N icolaieff in 1895* suspended a ring of paraffin between the two poles of an electromagnet, the plane of the ring being vertical and making an angle of 45° with the axis of the poles. The E.M.F. induced in the ring when the magnet is excited by an alternating current, sets up a displacement current which, by its magnetic reaction on the exciting field, creates a couple tending to make the ring turn and set itself perpendicular to the field. He excited the magnet first with direct current, getting a deflection due to the magnetic qualities of the ring, then with alternating current of the same intensity, causing a different deflection, the difference being due to the displacement current. The record of observations is not given in the paper, the author simply stating that the deflection was greater when the magnetic field was alternating than when direct ; and was greater the greater the frequency. For 12 eycles per sec. the increase was 9% over the constant magnetic field, for 15 cycles 12%; in this case also conduction would cause the observed effect. Blondlot.— Recently M. R. Blondlott+ looked for an electric displacement in a mass of air moving in a magnetic field. He forced a blast of air through a rectangular passage, two sides of which were pole faces of a magnet, the other two a pair of condenser plates. The plates were connected by a wire which was broken at the instant the blast was at its maximum, so that the plates should be left charged if there was any electric dis- placement in the mass of air. He calculated the expected effect and calibrated his electrometer to read it; the results of a number of experiments were invariably negative. Making use of this experimental fact, he then proves theoretically the absence of any electromagnetic action of a magnetic field on a displacement current. PrReEsENT RESEARCH. General Theory. The series of experiments herein described were undertaken in view of the continued uncertainty of the results of all effort to observe the magnetic effect of electric displacement, and in view of the fact that the method employed had certain advan- tages over those used heretofore. * Jour. Phys., vol. iv, 1895, pp. 245-254. + Jour. Phys., Jan. 1902, p. 8. 112 Whitehead— Magnetic Effect of Electric Displacement. In principle, the method is to subject a piece of dielectric to an alternating electric field and also to an alternating magnetic field, the directions of the two being at right angles in space ; to adjust the phases of the two to give the maximum effect of the displacement current reaction against the magnetic field, and to look for motion of the dielectric in a direction perpen- dicular to the plane including the directions of the electric and magnetic fields. In this form the idea was suggested to the Whitehead— Magnetic Hiffect of Electric Displacement. 118 writer by Professor Rowland shortly before his death. Some twelve years before he made the same suggestion to Dr. Louis Duncan, who constructed a crude form of apparatus, but cis) abandoned the work on account of the difficulty of obtaining a uniform field. : In each of four modifications of the form of the apparatus embodying the above principle, a block of dielectric was hung 114. Whitehead—Magnetic Effect of EHlectrie Displacement. rigidly at each end of a tight beam which was suspended hori- zontally on a quartz fiber attached at its center. The phase of either the electric or the magnetic field on one block being 180° from that on the other, the other field having the same phase for each block, the reaction of the displacement current on the magnetic field would be opposite at the two ends of the beam, causing a couple to act on the fiber suspension. Apparatus. First form.—The first form of the apparatus is shown in fig. 1, and fig. 2 gives a central section. AA are the rectangular blocks of dielectric, each attached to the beam D, which was constructed of bamboo or glass; B BBB are brass electrodes each turned so that its surface is a part of a circular cylinder with its axis coincident with the line of suspension of the beam ; this was thought to give the best approximation to a uniform electric field between the electrodes. Each pair of electrodes was connected to the terminals of a transformer giving 8800 volts at 133 cycles per sec. CC are circular coils of wire, one surrounding each pair of electrodes, the planes of the turns being horizontal; they are supplied with alternating current from the same generator which excites the electrodes. The magnetic field is seen to be vertical, the electric field horizontal, so the resulting deflection of the beam should be out of the plane of the paper at one end and in at the other. The whole rested on a wooden base, and each half of the apparatus was enclosed in a brass case, there being between the two only a small connecting trough in which the beam could swing, thus making the interior as small as possible and so minimizing the disturbance due to air currents. A close fitting brass cylinder inside the coil, a ring on top, and tin foil on the floor, all con- nected to the case, which was grounded, protected the dielectric from any electric field due to the coil; all possible secondary circuits were split, the openings being closed with hard rubber or fibre. The damping vane shown in the sketch was a strip of mica immersed in water, attached to the deflecting beam by means of a fine glass rod. The quartz fiber used was approxi- mately 102™ (40) long in all cases; it was enclosed in a glass tube fitted with a convenient torsion head permitting the adjustments of torsion and length independently; the fibre carried a small copper hook at its lower end which fitted into a corresponding hook sealed to the glass beam. Deflections - Pp Ss = of the beam were observed by means of the movements on a ground glass scale of the image of an incandescent lamp fila- ment reflected from a small mirror on the center of the beam ; during the later experiments the lamp was replaced by a Nernst j j 4 Whitehead— Magnetic Effect of Electric Displacement. 115 filament, which is beautifully adapted to this purpose. The distance of the scale from the mirror was 140. The connec- tions are shown in fig. 3. The generator, G, was a Westing- house “smooth-body,’ giving a pure sine wave, 1000 volts, 133 cycles; the transformers, T, T, T, were all Westinghouse make. The transformer T,, giving the high voltage, was built privately ; it was of closed magnetic type and had a ratio of 1 to 80. Bya suitable arrangement of switches 110, 200, or 400 volts could be put on the coils. The two magnetizing coils were connected in multiple and so that they worked together ; i. e., at any instant the fields were equal, parallel, and in the same direction. The electrodes were also in multiple, but worked in opposite directions, i. e., at any instant the fields were equal, parallel, but in opposite directions. In each circuit there was a reversing switch, RS. Calculation of Lffect Hxpected.—F ollowing is a calculation of the magnitude of the effect in the apparatus as constructed and experimented upon. Each pair of electrodes were 1°9™ apart; the dielectrics were blocks of rock salt, glass or paraffin, 1°" x 1™ x °63™ and they were hung with their square faces parallel to the electrodes, so that one-third the length of a line of force was within the dielectric ; thus V2-8800 being the maximum E.M.F. between the electrodes the proportion of it active on the dielectric is given by: vy = V2 - 8800 ae ee are) 1G Haiintensity of EALY. hoes 4/2. 8800 (QK +1) x63 (maximum value in volts). je = 116 =Whitehead—Magnetic fect of Electric Displacement. The density of the displacement current is ¢= pak = since ~ 4 dt the E.M.F. is alternating we have: Pe Sin. a ie da. and 7=G-im cosa 5, also ee = angular velocity = 27N = 7. 133 > dt Ta nK’ 4/2. 8800°" Qaedpamans Ty ae (OK 41) 63" SS cos a in C.G.S. electrostatic units. Ka 2. S800 Qa . 133. 10° Me = 4a ° (2K +1)X63' (8X10)? X10= cOS a, amperes Keg i OS A ollie K Peek ns amperes, effective, per unit cross section. Each of the coils for the magnetic field contained 1200 turns of No. 18 B. &.S. magnet wire; H, the intensity of the magnetic field at the center of these coils, as calculated with a neglect of the influence of the ends, was 200 7,7 being the current in amperes; as measured by the electromotive force induced in an exploring coil of known area and number of turns, H was 166 7, (area of exploring coil 25°™’, 400 turns ; observed E.M.F., with 2-4 amps. im coil, 33°5 volts, 133 cycles). The resistance of each coil was about 9 ohms, and the calculated value of the coefficient of self-induction was L = -109 henry; at 114 volts, 133 cycles, each took 1:3 amperes ~ which corresponds to a value 104 for L. If @ be the differ- ence in phase between the E.M.F. and current, i. e., the angle of lag, we have: _ amNL _ 6°28 x 188 X “104 ‘gpa: ae 9 Now consider the phase relations between the displacement current and the alternating magnetic field from the sketch of the connections. Since the difference in phase between the primary and secondary E.M.F’s of a transformer is approxi- mately 180°, the E.M.F. on the electrodes having passed through two transformations has returned to coincidence of phase with the generator E.M.IF’. and may be indicated by sina. The resulting displacement current has the phase cos a as shown above, i.e., differs by 90° from the generator E.M.F. The E.M.F. impressed on the coils has been transformed tan 6 = 9'3, whence 6 = 83° 52’ \ Whitehead—Magnetic Effect of Electric Displacement. 117 once, suffering retardation of 180°; owing to the self-induction of the coil the resulting current lags approximately 90°, and so, therefore, does the resulting magnetic field. Consequently, the displacement current and magnetic field are approximately 180° apart, that is, in the proper relation to give the electro- magnetic reaction. Actually, since the angle of lag in the coil is 83° 52’ instead of 90°, the effect as calculated for coin- cidence must be multiplied by -9942 = cos 6° 8’. The current in the dielectric is thus acted on by a force: | lq K 10°3. 1661-2 a= G3. A { .°9942. 10 Oe) bor 10 : = - fae dynes ment 10 2 when 1:2 amperes flows in each coil, 7 being the thickness of the dielectric, or the length of the displacement current acted on by the field, and H the intensity of the magnetic field. This force is applied in opposite directions at the two ends of the suspended beam, which was 17°78™ long, giving thus a couple of K 2°28 2K+1° 10% The angle of twist of a thread of length 7, radius 7, coefficient of rigidity n, acted on by a couple w is: 2 tee o——~ rm on dyne-centimeters. The length of the quartz fiber was 101-6; its radius was estimated by comparison under a microscope with the spaces of a grating ruled on glass, the grating space of which was known, and did not differ greatly from -0006™. The value of m being taken at 310" for quartz,* we have K ZSCLOEG X S38 K Ss = 4 4 ia abet poe 2K +1 ° «~x:0006**10°**3x10 2-3 Taking the value of K for rock salt as 5-8, we have ®=-173, which, since the distance from the mirror to scale was 140, represents a deflection of 2 1400 x‘173=485™", or more, since we have taken the tangent as equal to the are. The caleulation above assumes that the electric and magnetic fields remain constant through the range of movement of the dielectrics. It was of course foreseen that the electric field would be most intense at the center of the space between the electrodes and so would tend to hold the dielectric within that region ; nevertheless it was thought that a couple of the magni- . 37 radians. * Threlfall and Boys. 118 Whitehead—Magnetic Effect of Electric Displacement. tude above indicated would to a certain extent overcome this tendency. ‘The test for the true effect seemed to lie in a reversal of the sense of the deflection when the phase of either the electric or the magnetic fields was changed by 180°. Lesults—When the electric field alone was applied, the beam, as was expected, found a stable zero position near the center of the electrodes. With a fiber 20™ long this position could be upset by 10 to 20™™ on the scale, by a very small twist of the torsion head. This test was not so satisfactory when the long fiber was used, owing, apparently, to the large imertia of the syspended system, and to the arising of other disturbances within the time necessary for the torsion of the fiber to make itself felt. The zero point was always quite steady, having practically no oscillation, but was not always the same, varying within two centimeters. This indicated that near the center there was a region of fairly uniform electric field, and also that, owing to the mass and damping of the suspended system, the torsion of the fiber could not be depended on to give the zero position. The mass of the beam and dielectrics was from 2 to 3 grams, varying with the nature of the dielectric ; of this the greater part was in the dielectrics. Fibers of the size here required broke if the mass were 3 grams or more. The method of procedure was to allow the beam to come to rest under the influence of the electric field alone, the long time required for the oscillations about the central position to die out being another evidence that the field there was fairly uniform. Then the magnetic field was put on and the result- ing deflection noted. Then either the electric or magnetic field was reversed, the deflection noted, and so on. The deflection was generally small and quite slow im all cases, requiring con- siderable time to become steady; in most of the observations only the sense of the deflection was noted. Proceeding in this way, several hundred observations were taken ; they were gen- erally negative in result, that is, the deflection did not change in either direction or amount when either field was reversed. At times, however, there were indications of the effect looked for, as is shown by the following description : The electric field and then the magnetic field being put on, as described, with the values and conditions as given above, there resulted an uncertain deflection of about 1™™, which did not reverse with a reversal of the magnetic field. The circuits were then arranged so that 200 or 400 volts might be impressed upon the coils. With 200 volts a deflection of from 5 to 10™ was obtained, which, however, did not reverse with a reversal of the magnetic field; this deflection was towards a position which the beam tended to take when under the influence of the magnetic field alone. With paraftin as the dielectric the ——— a Se Wihitehead—Magnetic Lifect of Llectric Displacement. 119 proper reversal was obtained to the extent of 4 or 5™™ on two occasions, one with a reversal of the electric field, the other with a reversal of the magnetic field. In both instances the deflections were from a zero position constant within 1™™, and appeared as a slow motion immediately on closing the switch. The above mentioned disturbing effect of the magnetic field was always evident through all the experiments, but in this form of the apparatus in several instances there were distinct initial deflections in opposite sense to this tendency. When the switches remained closed long enough, the above disturbing tendency seemed to predominate regardless of the direction of the field. The question at once arose as to whether it was a magnetic or an electric effect. Experiments with bits of iron filing on the dielectrics, with hard rubber known to be slightly magnetic, with rock salt which gave no trace of mag- netic impurities, and with both direct and alternating currents, indicated that a part of this disturbing influence was due to the difference in the intensity of the magnetic field at the center and close to the side of the coil. For this reason only rock salt, glass and paraffin were used, as they appeared quite free from magnetic impurities; with them the disturbance was less than with sulphur and hard rubber, though it was still the predominating influence. Further experiments with rock salt several times gave evidences of the proper reversals to the extent of 2 or 3"; and with glass on one occasion the expected reversals of deflection were noticeable for six switch reversals ; these deflections were only 2 to 3™™. Very long waits between readings were necessary owing to the difficulty of obtaining a steady zero; this was probably due to air currents set up within the case caused by the heating of the coils when on the 200 volt circuit ; the six readings mentioned required one afternoon. On the next day the proper reversals of deflection were observed for four reversals each of magnetic and electric fields; they ‘were from 2 to 5™". It must be stated, however, that these proper deflections were taken from among a mass of attempts which resulted sometimes in no deflection at all and at others in deflections in the wrong sense. While it was sometimes possible to account for these by a steady shifting of the zero position, I still ques- tioned whether I had obtained the effect, and looked to the improvement of the apparatus. Second and Third Form of Apparatus.—In the second form the air space was reduced and the electric screening made bet- ter by enclosing only the electrodes and suspended system within the case, the coils being outside. The case was entirely of brass, the posts of the electrodes being set in insulating bushings. To prevent secondary currents in the cylindrical 120 Whitehead—Magnetic Effect of Electric Displacement. cases, they were each split down an element of the cylinder; these splits were covered and were on the front of the case, i.e., diametral planes through them cut the beam, in its central position, at right angles. The conditions were not improved by the apparatus in this form; if anything, the disturbance due to the magnetic field alone was worse, and it always caused a movement of the dielectric towards the side of the casing to which it happened to be nearer. Still thinking it a magnetic effect due to the more intense field near the coils, a single large coil which would completely surround the entire case and have its center in the line of the fiber, was wound. The field due to this coil would be uniform ar ound any circle concentric with the coil; the coil was 7:62™ high, had an internal diameter of 26-6e" and contained 360 turns of No. 15 wire. The conditions were not improved by the use of this coil, and it was still impossible to look for the true effect. This seemed to indicate that the disturbance was not magnetic, nor could it be due to electrostatic influence of the coil since the shielding was practically perfect. It was thought then that the electromotive force induced in the cylindrical metal case must set up a field in the slit down its side sufficient to cause the disturbances. To test this the slits were closed with solder, and new ones cut directly back of each of the outer electrodes; the disturbance disappeared almost entirely. Tests were then made with the single large coil and also with the two single coils; the constants for the large coil introduced no con- siderable difference in the calculated effect; the conditions in each of these series of tests were quite good; the electric field alone caused a good steady zero position ; on closing the switch of the magnetic field there was usually no deflection at all, only a slight oscillation; sometimes there was a deflection of 1™™ or 2™™, which, however, did not reverse on reversal of field and was pr robably, a survival of the old disturbance. Fourth Form of Apparatus.—As has been pointed out, the design of the electrodes in the experiments above described caused a position of stable equilibrium for the dielectrics, and it was thought that if the electric as well as the magnetic field were uniform and constant for all positions of the beam, the conditions would be greatly improved and practically as favor- able as the method permits. To this end the final form of the apparatus was constructed: The large coil described above was used for the magnetic field; as shown im fig. 4, the electrodes were two complete rings of brass, set concentric with each other and with the coil. The surfaces were carefully turned and polished, and each ring was split in one place to prevent its becoming a short circuited secondary circuit. The true cir- cular form of the ring was maintained by bridging the split — —_. Whitehead— Magnetic Effect of Electric Displacement. 121 with a strip of hard rubber; the splits in the two rings were in the same diametral plane. The rings were set on small, hard rubber chairs, and carefully levelled and spaced so as to be as nearly as possible the same radial distance apart at all points ; this distance was 1°9™ (3’’). In the earlier experiments this 122 Whitehead—Magnetic Lffect of Electrie Displacement. distance was varied, and 1°9™ was found to be the minimum practicable separation, anything less resulting in the dielectrics receiving a charge which would draw it against the surface of one of the rings; for any distance between the electrodes this always happened in damp weather. The coil was carefully sheathed with tin-foil which was connected to earth. The suspension hook on the beam was lengthened so as to reach into a glass tube shown in the sketch at M and the mirror placed on it there. By moving the source of light and scale in a circle about the apparatus, it was thus possible to take observations in any position of the beam. The walls of the glass tube scattered the light somewhat, but the intensity of the Nernst filament was so great as to always give a well de- fined line on the scale. The whole deflecting apparatus was suitably enelosed so as to be free from disturbance by air drafts. Calculation of Expected Lffect—With 8800 volts on the electrodes and with dielectrics of glass, paraffin and rock salt, the order of magnitude of the displacement current is not different from that already calculated. The angle of lag of the current in the coil, that is, the phase of the magnetic field, and also the intensity of the field, had also to be determined. The angle of lag was obtained by measuring the current taken by the coil at a known voltage and frequency. At 400 volts and 133 cycles this current was 10 amperes, the resistance being 4 ohms: iO = als whence L = 05 henry ; /16+835 L? ‘also the angle of lag, 6, is given by tan d= moe = 10°45, or 6 =)84" 289 The intensity of the magnetic field at various positions within the coil was determined by sending a current through it and measuring the E.M.F. in an exploring coil of known area and number of turns. At 200 volts the current in the coil was 5°3 amperes. ‘The exploring coil consisted of 400 turns of No. 33 wire, and had an effective area of about 25:8. Moving the exploring coil along a radius by equal steps, the following read- ings give the curve, shown in fig. 5, of variation of the inten- sity of the magnetic field with the distance from the coil; ordinates are values of the intensity and abscisse distances from the center, the coil having a radius of 13°6™. The de- flecting beam was 22°2°" long, so that the dielectrics swing at a radius of 11:1, and at this distance the field, with 5°3 am- peres in the coil, had an intensity of approximately 220, or 42 ee a OE Whitehead— Magnetic Effect of Electric Displacement. 128 per ampere, thus of the same order of magnitude as in the cal- culation for the first form of the apparatus. The suspension fiber was also the same, and so, therefore, the order of magni- tude of the calculated deflection. Position Volts Center 7°8 1 8°] 2 8°6 3 9°9 4 (near coil) Pt fesults.— With this apparatus, when the electric field alone was put on, the beam after a sufficient time always found a ee H per ampere. re G 8 is 12 14 2 * edge center position of equilibrium, in some places stable and at others unstable. The former seemed to be in a diameter which passed through the hard rubber supporting chairs of the rings, doubt- less owing to a slight concentration into the chairs of the field of force; a slight departure from this line was sufficient to cause the beam to wander to some other position, and the indications seemed to certify a quite uniform electric field. On putiing on the electric and then the magnetic fields, (5°3 amperes in coil) there was a deflection of from 2° to 3°™, which, however, did not reverse or show any regular difference in amount when either field was reversed ; it was found that the magnetic 124 Whitehead—Magnetic Lffect of F lectric Displacement. field when on alone gave a deflection in the same direction. Thus the magnetic field when on alone also had an effect on the position of the beam. With the beam at rest, when this field was made a slow drift away was generally seen, the beam com- ing to rest in some other position. Repeated efforts failed to locate single positions that it seemed to prefer, though in cer- tain neighborhoods the direction of the deflection seemed the same. In some positions there was no deflection, though these were never the zero positions for the electric field alone; the problem then seemed to bring the two zero positions together. Since the disturbance due to the magnetic field did not ap- pear to be the influence of the splits in the ring as before, for it seemed independent of the distance of the dielectrics from them, and since the intensity of the magnetic field was uni- form, it therefore seemed that direct electric influence of the coil or leading-in wires must be the cause, though the tin-foil screen seemed as perfect as possible. The attempt was then made to bring one of the positions in which the beam seemed unaffected by the magnetic field alone, into coincidence with a zero position for the electric field alone, by turning the coil into various positions about its center. This process was most tedious, involving as it did long waits for the beam to come to rest, and at its best it seemed only a hit-or-miss method. The condition sought, however, seemed so desirable, that repeated efforts were made to bring it about. One of them succeeded 3. and while the result obtained must be discredited in view of the failure of all attempts to repeat the proper conditions, and of other negative attempts, it is nevertheless thought that the following quotation from a note taken at the time should be inserted here: “this condition was obtained March 18th; the beam was allowed to come to rest under the electric field; this was then cut off and 400 volts put on the magnetic coil, which caused no deflection of the beam. On putting on both fields there was a slow deflection to the right of between 1™ and 2, about one minute being required. The magnetic field was then taken off and the beam allowed to move under the electric field alone; it resumed the former zero after one or two min- utes. The magnetic field was then put on reversed; there resulted a much stronger deflection to the left which was allowed to continue several minutes, resulting in a deflection of 5™, Repetition could not be obtained, due to the fact that after the large deflection the beam did not return to the origi- nal zero position. (The heating of the apparatus due to the large current in the coil (10 amperes) when applied for any length of time frequently upset the equilibrium positions.) The conditions, however, of the above observations were so favorable that my belief in the presence of the effect was Whitehead— Magnetic Effect of Flectric Displacement. 125 much strengthened after the many recent failures to detect any evidence of it.” Failing to repeat the condition as above described, a light strip of wood was placed along a diameter on top of the inner ring. This strip took up a sufficient charge to give the beam the position of delicate equilibrium when the beam was paral- lel to it, 1. e., directly over it; it could be rotated to any posi- tion on the ring without opening the case, by means of a device not shown in the sketch; the rod of the damping vane passed through a hole at its center. A number of experiments were made with the following order; the beam was allowed to find a stationary position under the influence of the magnetic field alone. ‘The interior being visible through the glass cover of the casing, the wooden strip was turned so as to be parallel to and directly under the beam, with the idea that the zero positions for the two fields would be brought into coincidence. It was found that in most cases any movement of the strip would upset the position of equilibrium due to the magnetic field. Frequently, however, the condition of coimcidence was ap- proached, and in all these instances when the effect was looked for the results were either spurious or negative. That is, if there was a deflection, as sometimes to the amount of 1™™ or 9™™, neither its direction or amount changed with a reversal of field; or often there was no deflection at all for either phase of -the field. Differences in deflection for the two phases of either field were now looked for; the wooden strip was discarded and the beam allowed to find a stationary position under the action of both fields. That is, the electric field was put on and a steady state reached ; then the magnetic field, resulting in a deflection of usually between one and two centimeters to a new position of equilibrium. The magnetic field was then quickly reversed and a change in the position of the beam looked for. Ina series of observations in which the conditions seemed perfect, no change at all could be noted when the field was reversed, there being either no deflection at all, or less than 1™ without regularity. In these experiments the coil only carried 2°6 amperes, giving a calculated effect one-half of that estimated above; 5°3 amperes, i. e., 200 volts on the coil, during the time required for the beam to come to rest, heated the interior to an extent sufficient, by reason of air currents or expansion of the ring electrodes, to cause erratic oscillations of the beam about its zero position. While it was thought that at the comparatively low frequency of the alternating circuit, 133 cycles per second, a possible lag of the displacement current, owing to molecular friction or other cause, could hardly make itself felt, it nevertheless seemed Am. JouR. ee Pg Surges, Vou. XIV, No. 80.—Avueust, 1902. 126 Whitehead—Magnetic Effect of Electric Displacement. worth while to shift the phase of either the electric or the magnetic field by a quarter of a period. For this purpose a two-phase machine was used, one phase being put on the pri- mary of the high tension transformer, the other directly on the magnetizing coil. This separates the displacement current and magnetic field by one-quarter of a period, if there is a lag of one-quarter of a period in the coil due to its self-induction, as was approximately the case in the experiments already described. The machine operated at 38 cycles, and 85 volts per phase; the resulting displacement current is thus 88 85 133 > 1107) of the value calculated for the first arrangement; at the lower frequency and voltage, however, the coil took 6°2 amperes, so Mee 5G 1-17 times that in the first that the magnetic field is 5 arrangement, so that the calculated magnitude of deflection is still appreciable ; the angle of lag is given by Q2nNL 237X + 05 Bai Sf, esis The cireuits were also arranged so that both electric and mag- netic fields might be put on the same phase or one on each ; this permitted, with the use of the reversing switches, a rapid change of phase of either approximately 90° or 180° between the displacement current and the magnetic field. In a series of observations with this arrangement there appeared to be no difference among the results of the several combinations of phase. The beam was allowed to come to rest under the electric field alone; on putting on the magnetic field there was the usual deflection, but there was no evidence of any change either in direction or amount of this deflection when the phase relations were altered at random. tan 6 = = 3°05, .. 0= 72°. Summary and Conclusions. The mass of the evidence of this research is against the pres- ence of the magnetic effect of electric displacement in an amount given by Maxwell’s expression. The single positive result obtained with the final form of the apparatus must be ques- tioned, for although the favorable conditions under which that result was observed could not be obtained a second time, it is thought that at times they were approached sufficiently to give traces of any effect as great as that noticed. The final form of the apparatus was undoubtedly that most likely to give results ; in it there appear to be only two influences which might pre- Whitehead—Magnetic Effect of Electric Displacement. 127 vent the effect sought. The first is a variation in the intensity of the electric field from pomt to point and the tendency of the dielectric to remain in the region of greatest intensity ; and the second, the presence of the damping vane. It is thought that neither influence was great enough to mask a couple of the value of that sought; as has been stated, the rings were carefully turned and adjusted in place so that their surfaces _ were the same distance apart at all points. Indications of any choice of position.by the beam in the electric field were of the | slightest, the stationary positions being very easily upset, and often changing by one or two centimeters between readings. The distribution of the electric field due to the coil, though uncertain, could not have departed greatly from symmetry about the center, and since the disturbance due to it manifested itself in deflections rarely exceeding 1°”, it does not seem possi- ble that the variations of intensity were great enough to account for the absence of visible effect when the displacement couple acting on the beam was reversed. In the earlier experiments several series of observations were made without the damping vane; no difference in the behavior or in the nature of the results was observed except the increase in time necessary for the beam to become stationary. Observations could not be made with the final form of the apparatus if the damper were taken off; the electric field was so nearly uniform that the beam would not retain a stationary position definite enough to be taken as a zero point. The following arrangement, independently conceived, but afterwards discovered to be an improved modification of the apparatus used by S. P. Thompson, offers a possible means of detecting a magnetic effect of the displacement current. An Annulus 1:9 thick, built up in laminations of sheet iron rings 3°18™ inside and 7°6™ outside diameter, was wound with a coil of several hundred turns of fine wire, which was connected with a telephone receiver. In the opening in this magnetic circuit was placed a cylinder of dielectric 2°54™ in diameter and 2°54™ in length. Flat electrodes were brought very close to the ends of the cylinder, but were not allowed to touch it. When now an alternating E.M.F. is applied to the electrodes the resulting displacement current. should set up an alternating field in the surrounding magnetic circuit, and so induce a current in the telephone receiver. The space between the electrode and dielectric prevents in great measure a possible conduction cur- rent due to conductivity of the material of the dielectric. With 8800 volts at 133 cycles on the electrodes, neglecting the air gaps, and with parafiin (K=2) as the dielectric, the displace- ment current density is: 128 Whitehead—Magnetic Hiffect of Hlectric Displacement. 1D 2472) S800 Ors. 183°) 10° oF ge GTA S 10") 105 ie and the total amount is 6°45 g = 3°34 X 10° amperes. The experiment was tried with paraffin and with hard rubber and no sound could be detected in either case. The question whether the telephone receiver would respond to such a small current was of course still open, nor could it be completely answered. The following approximation was, however, made: a conductor was placed through the opening of the iron annulus and included in a circuit with an ammeter, a resistance, and a source of alternating electromotive force in low values; the lowest division on the ammeter scale was ‘02 amperes, and the voltage was adjusted to give this reading, the telephone receiver giving a good note. Resistance was then inserted by steps up to about 100 ohms (inductive), apparently bringing the ammeter needle to zero; sound in the telephone receiver was still audi- ble, though faint. The experiment was performed very roughly and hurriedly, and is susceptible of considerable improvement. The writer’s thanks are extended to Professor Ames for his interest and kindness in furnishing every facility needed in the course of the investigation. The mechanical work was done by Mr. Charles Childs; for his skill and interest at all times the writer wishes to extend his appreciation. — It is proposed to carry this work further in both forms of apparatus. Physical Laboratory, Johns Hopkins University, May, 1902. Plowman—Ffelations of Plant Growth to Lonization. 129 Art. XVI.— Certain Relations of Plant Growth to Loniza- tion of the Soil; by Amon B. PLowMAN. In a series of experiments now in progress at the Harvard Botanie Garden, there have been observed some interesting phenomena in the relations of plants to electricity. The experiments have been of a widely varied nature, dealing with both static and kinetic charges, through a range of potential from 0°5 to 500 volts. Either platinum or high-grade carbon —usually the latter—was used for electrodes, and special care was taken to insure normal conditions of temperature, light, and moisture. The experiments were of course checked off by controls, always using at least two different sets of controls in order to avoid accidental errors. In a well-lighted greenhouse it is not a difficult matter to locate the different plants in such a way as to give fairly uniform light to all. For soil-cnltures, pots of the same size were used, filled with equal amounts of care- fully prepared soil, and supplied with measured quantities of water. The regulation of temperature presented serious difficulties whenever a considerable amount of current was used, for the resistance of the soil is very great and much heat is evolved in forcing the current through it. Thus a 500 volt circuit, joined through a body of soil 1025™ in cross-section and 40™ long between electrodes, gave a current of 0°2 ampere, and in one hour raised the temperature of the soil from 16° to 44°C. However, with a slight excess of moisture and a current not exceeding -05 ampere, it has been possible to prevent a rise of temperature of more than 38° above the normal; and in most eases the temperature has been kept within a range of 1° above that of the control. In the matter of temperature- regulation the water-culture method possesses many advan- tages. Hither by a slow circulation of the electrolyte, or by a more rapid circulation of water about the vessel containing the electrolyte, it is easy to maintain a constant temperature even when using currents of 2 amperes. In this way it is possible to introduce a very considerable electrical factor without seriously disturbing the other relations of the plants. Among other facts recorded in the course of these experi- ments is the following: Seeds placed near the anode are always killed by current amounting to -003 ampere or more, if continued for twenty hours or longer, while seeds placed near the cathode have in most cases been but little affected, and under some conditions have been apparently stimulated by such currents. 130 Plowman—Lelations of Plant Growth to Ionization. When the seeds were germinated in water this difference was most pronounced when a relatively heavy current was passed through the water for only a short time, in which case the seeds near the anode were killed, while those near the cathode were not apparently injured. If the current was allowed to flow for twenty hours or longer the ill effects were produced at all points between the electrodes, even when the current amounted to only ‘003 ampere, at a voltage of 2 or more. When the current was passed through ordinary sandy soil in which the seeds were planted, the same results were obtained at the anode, but a much longer time was required to extend the injurious effects to the region of the cathode. Indeed, so long as the current does not exceed about -08 amp. there is a considerable increase in the rate of growth of the seedlings near the cathode. In explanation of these phenomena the following provisional theory is offered. Whenever two points in any electrolyte are electrically charged to different potentials, the movement of the free ions in the solution* is given definite direction, and, if the differ- ence of potential is sufficient, further dissociation of the electrolyte follows. The anions with their negative electrons move toward the anode, and the cations with their positive charges pass to the cathode. Since the movements of ions in solutions are relatively slow,t it is reasonable to suppose that in the region of the anodes there would be a slight excess of positive ions, due to the rapid neutralization of the negative ions by the positively charged electrode. In like manner the cathode removes the positive ions in its immediate vicinity, and is consequently surrounded by a slight excess of negative ions. The more slowly the ions move through the electrolyte the more marked wiil be the difference of conditions about the two electrodes. How will seedlings respond to these differences of condi- tions? Itis clearly indicated by the results of our experiments that vegetable protoplasm is paralyzed and quickly killed by the conditions existing about the anode, while within certain fairly broad limits it is stimulated by the conditions about the cathode. While the dissociation of the atoms and electrical separation of the ions must bring about slight differences of a purely chemical nature in the region of the electrodes, yet * Ostwald and Nernst. Ztschr. phys. Chem. iii, 120, 1889. + Kohlrausch (Wied. Ann. 1. 403, 1893) has shown that, in an electro- lyte of unit potential gradient, the velocity in centimeters per second for certain ions is as follows :— CATIONS | ANIONS. H_ ‘00320 NH; °00066 | OH -00182 if ‘00069 Na ‘00045 Ag “00057 | Cl -00069 Ni ‘00064 Li ‘00036 K ‘00066 | Plowman—felations of Plant Growth to Ionization. 131 these mere chemical differences can hardly account for the effects upon the plants, even near the electrodes, and certainly not for certain effects at points mid-way between the elec- trodes. This conclusion is borne out by the following facts :— 1. When seeds are germinated in distilled water through which a weak current is forced, the O ions are in excess in that part of the solution where stimulation occurs, and the H ions are in excess where the plants are killed. But it may be shown that small quantities of hydrogen are not markedly harmful to plants. And the quantity of oxygen set free in distilled water by a weak electric current is certainly no greater than that normally present in ordinary: tap-water, such as was used for the controls; yet germination is often more rapid near the cathode than in the case of the control. Apparently, the effects are produced by the electrical charges of the ions, rather than by any mere chemical activity of the atoms. _ 2. When seeds are placed in solutions of various acids, bases, or salts, of a degree of concentration far below the “ killing point,” they will germinate quite as well as in ordi- nary distilled water. But when a current of electricity of sufficient strength to propel the ions is passed through the solution, that part about the anode becomes destructive to plant life. From these and other facts we conclude that negative charges stimulate, and positive charges paralyze, the embryonic protoplasm of these plants. This is strikingly in accord with the conclusions reached by Matthews* in his experiments on the nature of nerve stimulation, in which he shows that the sciatic nerve of the frog is stimulated by negative ions, and rendered less irritable by positive ions. In support of the theory here advanced the following facts may be mentioned :— 1. When a flower-pot containing several lupines of about four weeks growth is charged to relatively high potential (500v.) with positive electricity, the plants cease to grow, gradually lose their turgidity and finally die. On the other hand, when a negative charge is used these effects are not pro- duced, but the plants are actually stimulated. It is evident that, in the first case, the negative ions in the soil are drawn to the positive terminal, while the positive ions are driven to the plant. In the second case, the positive ions are drawn to the negative electrode, and negative ions are driven to the plants. 2. When seedlings are grown in an aqueous culture-medium through which a weak current of electricity is flowing, the * Science, vol. xv, No. 378, 1902. 132 Plowman—feelations of Plant Growth to Lonization. root-tips turn toward the anode. An attempt has been made to show an analogy between this movement and a similar turning of root-tips “up stream” against a water current. However, the analogy is of little value, owing to the fact that in the electrolyte there is a streaming of ions in doth direc- tions. Hence, the question is not so much a matter of the direction of the electric current as it is of the difference in effects of the two streams of ions. Upon examination of the conditions which prevail about roots growing in an active electrolyte, we find that the side of the root toward the anode is being bombarded by a stream of positive ions moving toward the negative electrode, while the side toward the cathode is exposed to the stream of negative ions on their way to the anode. Consequently the side of the root toward the cathode is stimulated, and that toward the anode is retarded, in its growth, and of necessity the root-tip curves toward the anode. Seedlings grown in ordinary soil show this curvature even more strikingly. The main axis of the plant is frequently curved almost 90° just below the surface ofthe soil. The curvature is toward the anode and away from the cathode, whether these be in circuit or isolated. 3. Normally, the plant body is electro-positive to the soil in which it grows. The potential difference appears to be a function of the physiological activity of the plant. The positive charge of the plant attracts the negative ions of the soil to its roots. Thus it seems that negative electrons are being constantly discharged to the plant as a natural condition of its life-activity. Any circumstance which would facilitate this electrical interchange we should naturally expect to be beneficial to the plant, while the reverse condition would be detrimental. . -It must be borne in mind that the phenomena with which we have been dealing are conditioned not only by temperature, light, aeration and moisture, but also by the nature of the electric current used, the solution-tension of the electrodes, the osmotic pressure of the electrolyte, the degree of dissociation of the electrolyte, the valence of the ions, the physical state of the ions, the chemical relations of the ions to metabolic processes in the plant, besides certain peculiarities of the living protoplasm with which we are working, and which should doubtless be taken into account in connection with each of the conditions named above. Evidently, any theory which may be advanced in explanation : of the various phenomena of plant-growth in the electrical field, must stand the most exacting tests of physical chemistry, in order to be worthy of serious consideration. Harvard University. Crook—Electromagnetic Alternating Currents. 188 Art. XVIl.—Demagnetizing Liffects of Llectromagnetically Compensated Alternating Currents; by ZENO E. Crook. Tue effect on the hysteresis cycle of passing an alternating current longitudinally through an iron wire, was given in a paper published in 1891, by Dr. G. Fienzi and Professor G. Gerosia.* Ata later date, Ignas Klemenicic published a paper on the relation of circular to longitudinal magnetism in iron and steel wires. He madea very brief mention of the effect due to alternating current. In the first named paper the writers found a very evident reduction of the area of the hysteresis cycle, and that a current of three amperes per sq. mm. was sufficient to totally destroy the hysteresis. When in this condition, the ascending and descending magnetization curves coincide and the effect of the magnetizing force approaches the - theoretical condition expressed by Frohlich’s formula aH 1+8H in which aand # are constants for a given specimen of iron, and | a is the saturation value of I. The writers thought the effect observed was due only to the demagnetizing power of the rap- idly oscillating circular magnetic field. Their reason for this was that there was no perceptible jarring or vibration in the iron. An attempt will be made in this paper to go still further into the study of the effects of alternating current on the magnetic properties of iron and steel. The main object of the study will be to discover if there is an effect due to the current inde- pendent of that producéd by the circular magnetism. The first question to be solved was how to eliminate the electromagnetic action, so that the effect of the current alone could be studied. This was done, approximately, by making use of the principle discovered by Ampere, that when two adjacent currents in parallel conductors flow in opposite direc- tions, the external field of force of the one tends to destroy that of the other. In order to be effective in destroying the internal as well as the external magnetic actions of the current, it was necessary to build up the iron from very thin laminze, and send the current in opposite oo in each alternate layer. *Rendiconti de Instituto Lombardo, vol. xxiv, fasc. x, April, 1891; Elec- trician, April 5, 1891; Ewing, Magnetic Induction in Iron and Other Metals, page 319; Wiedemann’s Annalen, vol. lvi, page 530. 134 Crook—Electromagnetic Alternating Currents. Two methods of studying the hysteresis were adopted, so that the results of the one might be a check on those of the other. First Method. The first method was a modification of the apparatus used in the Hopkinson’s bar and yoke method. The bar of iron, fig. 1, Tig. t. was made up of eighteen strips of sheet iron, each 40™ long, 1-9" wide and -045°" thick. These were joined at the ends, and insulated from each other by strips of shellacked paper so that a current would flow through each successive strip in the opposite direction. Allowing a small amount for the effect due to insulation between the iron strips, it was estimated that the internal magnetic action of a current flowing through the iron in the manner described above, was approximately one- Bie. 2: 2 », a + T aes Crook—Electromagnetic Alternating Currents. 135 eighth of that due to a current of the same current density j flowing directly through the iron strips in multiple. j The yoke, fig. 2, used was one designed by Prof. D. B. | Brace and already described.* The advantage of this apparatus over the old form of yoke is that at all times during the hysteresis test the total induction _ --_— ean _be measured without changing the susceptibility of the 7 magnetic circuit, and the only change in the induction is that caused by a change of current in the | magnetizing solenoid. Diagram I. rere — = 25 Sane Eeees Esssseseea iat a ee auc ected Sees aerae | eee i eee sea ence ute) a i 8 Hisaee Ee, aul _. ieseeeeeteetece ae Hate peuevistasessaviasa gtaseszaass BETT6 INSTITUTE OF TECHNOLOGY, oe FEE SEzazongssesusverey ensbsteens eres The alternating current used for demagnetization was a obtained from a 50-volt circuit, transformed from a-1000 volt, b 40 h. p. Westinghouse dynamo. The frequency of the alter- nating current was 133 periods per second. The three hysteresis cycles given on Diagram I were all taken = the same evening and under practically the same conditions. =. * This Journal, vol. xi, p. 365, May, 1901. oe ~~ 136 = Crook—Llectromagnetic Alternating Currents. The curves were taken in the order in which they occur on the plate and were plotted from the readings given in Table I. Curve 1 is the normal hysteresis cycle. Curve 2 is a cycle taken with an alternating current density in the iron to 10 amperes per sq. mm. TABLE I. PB: i. Cycle 1. Cycle 2. Cycle 3. 0) 174 120 1443 lis 846 600 1815 6°3 QAAT 2010 S252 9°45 4329 4AQ45 4890 12°6 5400 _ 0415 © 5706 Lv 6279 18°9 6765 6750 6939 25°2 7500 7440 TOs 31°5 75930 7686 7740 VAS ab 7594 7604 7689 18°9 fpey el 12:75 7320 12°6 6675 6630 6600 6°3 5730 5655 5331 0 3285 3128 2232 6°3 — 2418 — 2550 — 3525 126 —5750 —5750 — 6600 18°9 —6999 —6747 —7011 pA es — 7677 — 7446 — 7560 31°d — 7983 — 7800 — 79206 BH<2 —7794 — 7650 — 7776 18°9 — 7560 — 7360 — 7440 12°6 —7215 — 6086 —6981 6°3 —6204 - —5765 - — 5607 0) — 4050 — 3666 — 2265 6°3 1863 2100 3249 A close inspection of the curves will show that the reduction of the area of the cycle is directly proportional to the reduction of the width and also to the reduction of the residual mag- netism remaining in the iron when the magnetizing force is reduced to zero. This being the case, the problem can be considerably simplified by studying the effects of the alterna- ting current on the residual magnetism from a constant mag- netizing force, assuming that the effect on the hysteresis cycle is directly proportional to this effect on the residual mag- netism. The curves in Diagram II were taken to show the effect on the residual magnetism of varying current density in the iron strips in series. They were plotted from the readings given in Table IJ. Ordinates represent total induction and abscissae _— Crook—Electromagnetic Alternating Currents. 137 represent current density per sq. mm. Curve 1 shows the effect due to a constant current; curve 2, that due to an alter- nating current. Diagrams IT and ITI. Curve 1 (Diagram II1) shows the reduction of the residual magnetism due to an alternating current of varying density passing through the iron strips in series. 138 Crook—Llectromagnetic Alternating Currents. TABLE II. Current density Total residual induction. per sq. mm. For curve 1. For curve 2. 0) 745 745 2 740 712 3 743 684 5 743 665 7°95 740 630 9 710 580 10 695 350 15 580 360 19°2 520 290 Curve 2 (Diagram IIT) shows the corresponding effect due to an alternating current passing through the iron strips in multiple. Readings for these curves are found in Table III. TABLE III. Current density Total residual induction. per sq. mm. For curve 1. For curve 2. ‘0 (22 122 728 719 Bite alae "56 714 708 84 708 689 1°25 700 670 1°68 690 654 2°2 682 631 2:5 675 618 Second Method. The second method of studying the alternating current effect on hysteresis was carried out in the same way as the first, the only difference being in the apparatus used. Instead of a number of narrow strips of iron connected in series, the iron specimen was made from two thin sheets of iron, separated by shellacked paper and rolled into a compact tube. The iron sheets were each 56™ long, 50™ wide and 018 thick. Along the edges of the plates corresponding to the upper end of the tube were soldered “leading-in” con- ductors, short distances apart. This was to insure a uniform current density in all parts of the plate. The edges of the plates at the other end of the tube were bared and soldered together, so that a current entering the upper edge of one plate would flow down, across the soldered junction, back on the other plate and out by the leading-in conductors soldered to its edge. 3 Crook— Electromagnetic Alternating Currents. 189 The tube was 50™ long and had an inside diameter of 2°5™. Inside of the tube was a core of wood with a copper wire running along its cylindrical axis. This system is practically equivalent to sixteen concentric iron tubes ‘018™ thick, with their ends so connected that a current of equal current density flows through each alternate one in the opposite direction or _ through all of them in multiple, according as the experimenter desires. The magnetizing coil was of the same length as the iron cylinder and wound with 300 turns No. 16 copper wire. The test coil used for measuring the magnetic flux was wound on a wooden spool made to slip over the magnetizing coil and sufficiently large and heavy to fall freely and uniformly when liberated. The cylinder was mounted inside the magnetizing coil in a vertical position, about five feet from the floor, and so arranged that the test coil would fall from the center of the cylinder to about two feet from its lower end. In this way it was possible to measure the total magnetic flux in the iron. The other apparatus was the same as that used in the first method. It was found that the amount of residual magnetism remain- ing in the cylinder after applying a strong magnetizing force, was very small, and all attempts to show the demagnetizing effects on the hysteresis cycle were unsatisfactory. However, the reduction of the residual magnetism by the alternating current was quite satisfactorily shown and the results are as given below. The residual magnetism’ left in the iron was stronger when an alternating current was present during magnetization. Because of this, the alternating current was thrown off each time the magnetizing force was applied, and readings were taken to find the residual induction before again applying the alternating current. These all gave almost constant results. The readings were all reduced to the mean value. Readings taken while the alternating current was flowing and those taken after it was thrown off were nearly always the same. However, in curve 2 the values of the residual magnetism after the alternating current was thrown off were different and are represented by the dotted portion of the curve. The alternating current was applied in four different ways and the effects studied. First, it was passed through the iron plates in series, so as to get the effect of the magnetically compensated current. Second, it was passed through the plates in multiple so as to get the combined effect of the cur- rent and circular magnetism. Third, it was passed through the iron plates in multiple and back through the copper rod. Fourth, it was passed directly through the copper rod. The 140 Crook—Electromagnetic Alternating Currents. curves, plotted from the values given in Table IV, are given on Diagram IV and are numbered to correspond to the order in which they are here mentioned. Ordinates represent total induction, and abscissae, current densities per sq. mm. 3 Diagram IV. MABSACHUSETTS INSTITUTE OF TECHNOLOGY, Curves similar to those given on Diagram IV were taken with the frequency of the alternating current reduced one half. They are given in Table V, and plotted on Diagram V. i oe ~~ ve Crook—Electromagnetice Alternating Currents. 141 The effect due to a direct current of varying current density is shown in Diagram VI. The direct current was applied by suddenly closing the circuit through the iron. A slow build: ing up of the current had no effect on the residual magnetism. Diagram V. This shows that the effect was due to the sudden impulse of the current through the copper rod or through the iron. Readings for these curves are given in Table 6. AM. Jour. Sc1.—Fourts SeRies, Vou. XIV, No. 80.—Aveust, 1902. 10 142 Current density per sq. mm. O° ae ~T Or Or ie) H He CO ND DO DS eS et pe & wo Or ie) Current density in iron. 0) 25 9) , ~yJ Or Or Or Hm HR OO OO DD Nw ee eb . — on S Current densi ty in iron. O . “25 5 “75 af e 1°5 The hysteresis cycles given on Diagram I shows that the alternating current as magnetically compensated has an effect Crook—Electromagnetic Alternating Currents. TABLE IV. Iron and Iron in rod in Tron in multiple. series. Rod alone. series. F054 1051 1045 1055 962 8628 861 ee 856 660 702 1003 760 492 533 ge 728 286 340 oe 705 Ane oes ao 970 681 “ee Lee hae re is. 80. 163 aie oe Crise Pieces Ra S23 935 meee Bees Deere 903 Ee 8s une oat NS ries 870 TABLE V. Total residual induction. ‘Gua Sos eee | — Tron in Iron and rod Tron in multiple. in series. Rod alone. series. 1150 1146 1150 1150 1090 Saba mee pee 1004 1012 1010 TI25 865 and 855 900 908 1095 725 and 695 a ike Pert: ee | 665 and 610 hares eee age ay ay an =yiaeh 658 686 1045 560 and 465 esos SEOe gues fe om Lik, ® 400 460 975 fiat aS ed See 945 te neds 179 230 seta ae se 45 132 870 TABLE VI. Total residual induction. (aa SS ay Tron in Iron and rod Iron in multiple. in series. Rod alone. series. 1000 1001 1000 1004 996 tpt se rots sees thes 990 940 920 1000 980 Eee ersten Ee aes ete 875 850 1003 rere s 820 792 10083 on the magnetic induction in iron. Crook—Electromagnetice Alternating Currents. 148 The eurves on Diagram II show that for low current densi- ties, the reduction of the residual magnetism in iron, or the reduction of the area of the hysteresis cycle, is proportioned to Diagram VI. HE Wf fF jaa Sneeneeece So) eiiuusesaaiaasz Sssesserscsesszevseseess Suan eases PeBeaGEBeaCuuaueaes HH Ppp rity ry BSE tE teeta Serene wetiens SRSRERRaS See aN GEES eRe Se See Sirti smite fecal SSeS ei He ieee Henini SES LeneeEeel HoH Sree acetal eras bd nt ertae? ee SSSSCGSSU GEESE Se rT Ener snes SEaceeSESse’ Seduce ewe detain teen ects BEE aisssseesercesseraas cngaee siti 33.amSg tare 20s, USSR RS eee Sel Hert SBu8BRawe hee ror HIER IHTET Heed iessparttesspossiostioast as MASBACHUGETTS INSTITUTE OF TECHNOLOGY, the strength of the current. Above 7°5 amperes per sq. mm. this relation does not hold, but heating effects and the effect 144 Crook—EKlectromagnetic Alternating Currents. of the residual magnetism in the yoke come in to affect the induction measurements. If the values of curve 1 are sub- tracted from those of curve 2, the result is nearly a continua- tion of the straight line which gives the effect at low current densities. The similar curves on Diagrams IV and V taken by the second method, and at different frequencies, show that the effects of the alternating current on the residual magnetism in iron are different for different frequencies, that for the lower frequency being the greater. Curves 3, Diagrams IV and V, show that the total reducing effect of the current is approximately proportional to the strength of the current. Curve 3, Diagrams IV and V, show the reducing effect of the external circular magnetic field from a current flowing through the central copper rod. Curve 4 shows the effect of passing a current down the central rod and back on the iron. The force at a point in a metal tube due to a longitudinal current in the tube is expressed by the formula SS ere (r°—r,”) in which F is the force, w the current density per unit area of the cross section, 7 the distance of the point from the axis of the tube, and 7, the inside diameter. From this it is seen that at the inner surface of the tube, where r=7,, the force is zero, : : ee while at the outer surface, where 7=7,, the force is a The . 2 e e average force in the tube due to a current flowing longitudi- e . e 7 e e nally along it is proportional to — where 7, is the mean radius Tv 3 of all points in the tube. The magnetic force at a point outside a linear conductor is expressed by | 24 F = — ‘: where 2 is the total current and 7 is the distance of the point from the axis of the conductor. It is, therefore, evident that the average force in the iron due to a current flowing along its e e e e e 2 e e cylindrical axis is proportional to = ithe magnetic force in ais the iron when the system was connected for taking curves 4, Diagrams IV and V, was therefore one-half what it was when it was connected for curve 3, and if the reduction of the residual magnetism was due to the circular magnetic flux alone, we Crook—Electromagnetic Alternating Currents. 145 should expect the values of any point on curve 4 to be one- half that of a similar point on curve 3. Any added effect caused by the presence of the electric flow in the iron would tend to make curve 3 approach curve 4, and in fact it is found that the latter falls below the former. If the apparatus used in the second method was as effectual in reducing the circular magnetic effects as was expected, eurve 1, Diagram IV, can be taken as giving an approximate measure of the reduction of the residual magnetism by an alter- nating current flux, with a frequency of 133 alternations per second; and curve 1, Diagram V, a similar measure when the frequency is at 66 alternations per second. The effect of the magnetically compensated current as given by these curves is about one-fourth of the total effect of the current and circular magnetic effect together. Other Methods. The following experiments were made to study the effects of electric oscillations on magnetized plates (fig. 3 A) placed in a magnetizing solenoid of very thin sheet iron (trunk cover- ing) cut into strips 7 inches X3/4 inch and separated by sheets of mica made to project past the edges of the iron an eighth of an inch. This system was connected to a Holtz machine and Fig. 3. the spark gap adjusted so as to get a rapidly oscillating dis- charge. The magnet, after being magnetized to a maximum amount of residual magnetism, was placed carefully in the field of a sensitive magnetometer. This magnetometer was made of an astatic magnetic system suspended by a silk fiber in a glass tube. The magnet was so placed that the mag- netometer was deflected a few degrees from the meridian. The system was carefully tested to prove the effect produced was not due to conditions external to the iron. Any disturb- ance in the magnetic field of force thus produced could be 146 Crook—FLlectromagnetic Alternating Currents. readily detected with a telescope and scale. It was found that an oscillation of the static charge in the “ magnetic condenser ” produced a demagnetizing effect which could be readily detected with the magnetometer. The effects were lacking when a thin foil condenser was substituted for the iron one. The residual magnetism of the laminated electro-magnet was also found to be affected by the oscillating electric charges, when connected in series, fig. 3 B, with a condenser to the terminals of the static machine. The amount of this effect was approximately equal to the effect when the magnet was used as a condenser. | Fig. 4. Another test, fig. 4, was made by placing a pile of these japanned iron sheets between terminals of tinfoil which were insulated from the iron by mica. This proved to be just as effective in producing results as the other method. The frequency of oscillation was an indeterminate factor and did not seem to affect the results, as the demagnetizing effect was apparently produced during the first oscillations. A single spark between the terminals of the machine, in most cases, proved to be as effective as a continuation of the oscillatory discharges. Nore.—This work was done at the University of Nebraska under the imme- diate direction of Dr. D. B. Brace, and much of the success of the investiga- tion was due to suggestions offered by Dr. Brace and by Professor B. E. Moore. Physical Laboratory, University of Nebraska, Lincoln, Nebr. Coleman—Nepheline and other Syenites in Ontario. 147 Art. XVILI.—Wepheline and other Syenites near Port Cold- well, Ontario; by A. P. COLEMAN. A FEW years ago some very interesting dikes of a rock con- taining analcite named “heronite” or analcite tinguaite were described by the writer from the north shore of Lake Superior between Heron Bay and Peninsula on the Canadian Pacific railway;* and the opinion was expressed that nepheline rocks should be found connected with them somewhere in the region. Dr. Adams also has suggested the same idea, basing his belief on some rock specimens from the region of Peninsula in the Geological Survey collection. They are augite syenites of an unusual kind often associated with nepheline : syenites.t In connection with an excursion to the iron range of the Slate Islands an opportunity was taken to examine the railway and shore near Port Coldwell, and it was intended to visit Pic Island a few miles off shore, where Professor Pirsson and others have suggested that nepheline rocks would probably be found, but unfortunately no suitable boat could be got at that little harbor, and this had to be given up. No syenites of any kind were found between Heron Bay and a point three miles east of Peninsula, where augite syenite had been obtained a few years before; but west of Peninsula, more than half way to Port Coldwell, considerable stretches of nepheline syenite were discovered. So far as the study of the specimens has gone one can say that a great area of syenites and associated rocks rich in alkalies, derivatives of a magma differentiated into a whole series of related species, like those so elaborately described by Broégger in the Christiania region of Norway, occurs in this region. The first rock of the group, going west, is the dark. augite syenite which commences three miles east of Peninsula, and with some interruptions of red syenite and more basic rocks extends to a long trestle at mile 818, a distance of nine or ten miles, with an unknown width. From the trestle west to a cutting beyond Peninsula, the prevalent rock is a gray or purplish gray nepheline syenite, having an extent of about four miles. It is probable that detailed mapping of this little _ explored region would show large areas of this syenitic group of rocks, including Pic Island, and it is hoped that in the future these interesting eruptives may be studied more at length. The only previous references to this group of syenites are to * Bureau Mines, Ontario, 1899, pp. ee ae and 1900, pp. 186-191. + Jour. Geol., vol. viii, No. 4, PP. 322 148 Coleman—Nepheline and other Syenites in Ontario. be found in the reports of the Geological Survey of Canada,* where rocks containing red and white feldspar, some grains of orange-red elaeolite, and a few zircons, are said to occur in Pic Island and the mainland to the north; and of the Bureau of Mines,t where the occurrence of augite syenite and other associated rocks is referred to, though the nepheline rocks were overlooked. Acknowledgments must be made to Pro- fessor L. V. Pirsson and Dr. H. 8. Washington for having been good enough to send chips and larger specimens of various nepheline syenites and related rocks from other localities which have proved most useful for comparison; and to Profes- sor Pirsson for suggestions as to rock relationships. Nepheline Syenites. The syenites and associated rocks are very well exposed between miles 818 and 822 in the numerous rock cuts and cilffs where the railway winds along the rugged shore of Lake Superior, so that an almost continuous section is presented. The first nepheline syenite observed is just east of the long trestle at Red Sucker lake, where it forms irregular dikes and larger masses in gabbro, which appears to be the older rock of the two; and similar relations are found at the rock cut west of the trestle, though red syenite interrupts it at the third cutting. Beyond this, toward the west, hills of nepheline syenite rise 200 or 300 feet above the lake and continue with few interruptions to Port Coldwell station and the next cutting beyond it, the last point where it was observed being a little beyond mile 822. The second cutting west of the station is in red syenite. The rock varies from almost compact to very coarse-grained kinds having crystals an inch or more long; and in color from pale to dark gray, sometimes running into purplish tones or having brillant red spots. The black horn- blende and augite crystals stand out sharply giving a fresh look to the rock, which unfortunately is not borne out in thin sec- tions. In some specimens the hornblende crystals are long slender prisms, but in others they are short and _ stout. The different textures are often mixed intimately, fine-grained parts enclosing coarser grained ones or the opposite; and large or small blocks of the gabbro mentioned above are enclosed in the nepheline syenite. Dikes of a fine-grained pur- . plish gray rock, sometimes with the look of an amygdaloid, eut the syenite; and last of all, there are sharply defined dikes of black diabase. In general appearance the nepheline syenites are very dif- ferent from those of Eastern Ontario, never showing the * 1846-7 ; also 1863, p. 80. +1897, p. 147. Coleman—Nepheline and other Syenites in Ontario. 149 eneissoid structure so common there, nor having dikes of peg- matitic rock consisting of large individuals of nepheline and muscovite. Nor are they like specimens from Barkevig, . Norway, nor Litchfield, Maine, but some of them have much the appearance of specimens sent by Professor Pirsson from Highwood Mts., Montana, and Red Hill, Moultonborough, New Hampshire, having a tendency to flat plate-like forms of the feldspars, and long prisms of the darker minerals. These would apparently be classed by Professor Brégger as foyaites, though unlike a specimen of foyaite from Lougenthal, Norway, sent me by Dr. Washington. In the considerable number of specimens collected near Port Coldwell four fairly well marked types may be distinguished, so far as megascopic structure is concerned : 1. Medium to coarse-grained gray rocks having a dioritic appearance with light and dark minerals in about equal amounts and the grains isodiametric. 2. Medium-grained, reddish, purplish or violet-gray rocks, with about twice as much of the lighter colored minerals as of the darker ones, and with a tendency to plate-like or elongated forms in the minerals. 3. Violet-gray, fine-grained rocks with porphyritic feld- spars and other minerals. 4, Narrow veins of coarse-grained rocks, often mottled with red, gray and black. There are, however, many intermediate varieties between the four here mentioned, illustrating the usual variability of . the nepheline rocks. 1. The first variety occurs as fresh looking material about two miles east of Port Coldwell, and was supposed to be diorite when collected. The white minerals are nepheline, orthoclase, and a less amount of finely striated plagioclase having a very small extinction angle, probably oligoclase ; all badly weathered and turbid, the nepheline sometimes changed into a brown- ish substance having aggregate polarization, perhaps a zeolite. The dark minerals include hornblende in fairly well formed crystals having a pleochroism of dark green, brownish green and brown, and an extinction angle of 23° ; and also augite in about equal ‘amounts, sometimes enclosed in the hornblende. The augite has a slight pleochroism, sea-green, gray-green and brownish green, but its extinction angle is normal and the nearly rectangular cleavages in cross sections show that it is really a pyroxene. The only accessory minerals noticed are magnetite and apatite, both in considerable quantities. A very similar but duller rock occurs in the first railway cut west of Port Coldwell, with the difference, as seen under the microscope, that the hornblende is dark brown and the augite 150 Coleman— Nepheline and other Syenites in Ontario. grayer and not pleochroic. One or two large masses of magnetite and serpentine probably represent olivines com- pletely decomposed. 2. The gray or purplish gray variety, with relatively small . amounts of the dark ingredients, contains all the minerals mentioned as belonging to No. 1, with the exception of the probable olivine; but the ferro-magnesian minerals are, of course, less in amount, and occasionally a little brown biotite occurs, in addition to the hornblende and augite. The red color of spots in the rock is due to infiltration of iron oxide in portions of nepheline completely changed to zeolites, and the usual reddish or purplish tone of the rock is due to the general diffusion of the same oxide. As distinguished from the previous variety this one is leucocratic. In some examples the minerals have plate-like or long prismatic forms with a suggestion of the trachytic structure. In one section the augite is almost entirely replaced by hornblende, often dark brown in the middle and green at the edge with very deep colors but not strongly pleochroic, perhaps barkevitic in character. 3. The porphyritic varieties of the nepheline syenite occur partly a mile or two east of Port Coldwell and partly to the south of the station near the harbor. Specimens from the former locality are dark bluish gray, fine-grained, with por- phyritic feldspar, nepheline (rarely) and hornblende crystals. One thin section from mile 819 shows very small crystals of nepheline having the prism and basal planes, enclosed in ortho- clase and possibly oligoclase, as well as in hornblende, the latter mineral forming sieve-like structures, the holes being . filled with lighter minerals, a good example of poecilitic inter- growths. The other minerals are augite, magnetite and apatite. A second specimen shows less of the poecilitic intergrowths but contains one or two long porphyritic prisms of nepheline. Porphyritic examples from south of the station have a purplish gray ground in which bluish erystals of feldspar and black crystals of biotite are embedded. The groundmass does not differ much from the former rock, but the numerous phenocrysts are orthoclase, oligoclose and brown biotite, having strong dichroism. 4, The fourth variety forms narrow pegmatitic veins in the other varieties, and consists of the same minerals but of larger dimensions, sometimes more than an inch in length, though never rivaling the giant nepheline pegmatites of Hastern Ontario, as described by Dr. Adams, with crystals more than a foot long. The nepheline in the Port Coldwell specimens is often changed to a turbid orange-red material, mentioned by Sir William Logan as elaeolite,* the feldspars (orthoelase) are * Geol. Can., 1868, p. 81. Coleman—Nepheline and other Syenites in Ontario. 151 pale gray, and the hornblende prisms black, making a very showy rock. In spite of the striking differences in appearance of the varieties mentioned above, the range of minerals found in the thin sections examined is not great, much less, for instance, than in the nepheline rocks of Dungannon and York branch in Eastern Ontario,* and none of the rarer minerals have been found by myself, though zircon is mentioned in the 1863 report. The absence of muscovite, scapolite, sodalite, and of the usual microcline and microperthite is peculiar ; though in some cases weathering has gone so far as perhaps to obscure the structures of the feldspars. Augite Syenites. The other important group of rocks in the region includes the augite syenites, which occur in two well marked varieties, one dark brownish gray to black in color, coarse-grained and with more or less of a plate-like character in the feldspars ; the other red or reddish gray, finer grained and usually granitic in texture. The first variety is much the more extensive of the two and will be described first. In the dark variety, which is no doubt the trap that Logan reports from the region, the feldspars are the prominent ingredient, forming broad plates or narrow shining strips, often carlsbad twins, attracting the eye in the sun; while the relatively small amounts of ferro-magnesian minerals escape notice. While dark brownish gray to black is the prevalent color, there are phases of a dull brown or a dull red; and weathered glaciated surfaces may even be white by the bleach- ing of the feldspar, when the augite and magnetite show as angular or black filling material between the feldspar crystals, which tend to be idiomorphice. The syenite is always coarse-grained, the crystals averaging about a quarter of an inch in length, and also in breadth when seen broadside, but often only a tenth of an inch in cross sec- tion. There are coarse pegmatitic veins in the finer grained rock having individuals of feldspar an inch or two in diameter, and often fairly well built out in occasional cavities. As this rock has been quarried by the railway for bridge construction, etc., it is easy to get fresh material. Thin sections consist of feldspar in more or less idiomorphic forms with augite wedged in between, resembling, so far as one ean tell from a description, Brégger’s laurvikite.t The feldspars show no twin striations but have partly the appear- ance of microperthite and partly of microcline. They are * See Bureau Mines, 1899, Corundum and Other Minerals, p. 205, etc.; and Corundiferous Nepheline Syenite, p. 250, etc. + Zeitschrift fir Kryst. u. Min., Band 16, 1890, pp. 29, 30. 152 Coleman—Nepheline and other Syenites in Ontario. fairly fresh and in some directions have a handsome bluish shimmer. No nepheline nor sodalite nor quartz was observed. The dark minerals are chiefly augite with brown interior and dark green exterior, but some dark green and brown horn- blende, and some magnetite occur also, as well as apatite. An analysis of this rock made by Mr. A. H. A. Robinson of the Chemical Department of the School of Practical Science, Toronto University, gives the following results in column I: ip II. TUL, s) LO pee eseie i 2 58°81 58°88 °980 AOL Ge a 13°37 20°30 131 FeQ.0.6) ene 3°63 024 ReQ 2. See ee soy is ee "097 MnO 2 oe ad eee 0°20 ae | Wee 22 acc vslnis eee 0°51 0-79 012 Oe Oe VRE Lite yey 3°89 3°03 069 NG AD NOs oT Sb eee 4°96 5°73 080 HO Aikc2 ee Ee 5°49 4°50 056 HOt D008 eee 0°29 1:01 H,O above 100° C. ..-. 0°75 MSOs cb sok Ne ok e te O75 iG) ai. 2 vides. Pegientel 0°31 0°54 Total 2 -isses opeet AVOOSOG 100°99 Specific gravity at 17°°5 C., 2°75. For comparison an analysis of Norwegian laurvikite from Byskoven, Laurvik, by A. Merian is given in column IIL.* The two analyses agree fairly closely except for the relative pro- portions of alumina and of ferrous iron oxide, which differ greatly. The analysis shows the rock consists largely of micro- cline and microperthite, the small amount of magnesia and large amount of ferrous oxide that the augite must consist mostly of the hedenbergite molecule. The amount of alumina, though smaller than in the laurvikite, is that which is required by the soda and potash to turn them into feldspars and is therefore correct, as shown in the molecular ratios given in column III. . Associated with the dark augite syenites with plate-like feld- spars are numerous other varieties in much smaller amounts, some merely having the red color of the ordinary syenite, due to diffused hematite particles, but with the same ingredients and the same shape of the feldspars; others differing more widely in appearance and composition, but all more weathered and less satisfactory for study with the microscope. It will be sufficient to refer to the kinds having granitic structures, * Thid., p. 30. Coleman—Nepheline and other Syenites in Ontario. 158 grains with equal diameters. These are on the average finer grained than the Laurvikitic syenite, and may be divided into leucocratic red syenites with comparatively little of the ferro- magnesian minerals; and melanocratic varieties containing more than half dark minerals. It must be admitted that the term leucocratic syenites is not happy for the less basic varie- ties, since they are strong red and not white or pale colored. Several specimens from east of Port Coldwell are in reality quartz syenite consisting of feldspar pegmatitically intergrown with quartz, and small quantities of hornblende, augite, mag- netite and apatite. The feldspars, which tend to be por- phyritic, so far as their weathered condition permits one to decide, are orthoclase, microcline and oligoclase. These rocks seem to have the same composition as Brégger’s nordmarkites, though no mention is made of pegmatitic intergrowths in the latter rocks.* Aegirite has not been recognised in the rocks from Port Coldwell, another point of distinction. The melanocratic syenites, consisting to the extent of at least half of dark colored minerals, are dark gray rocks, usually with a red tinge, not very coarse-grained, with about equal diam- eters to the grains. The light colored minerals are ortho- clase, some plagioclase and occasionally nepheline; the dark ones hornblende, pale blue-green augite and brown biotite in not far from equal amounts: while magnetite and apatite are always present, the latter often as numerous large prisms. They appear by analogy to be related to the essexites. Plagioclase Rocks. Three kinds of plagioclase rocks accompany the syenites of the Port Coldwell region, coarse-grained gabbro-like rocks older than the syenite and penetrated or carried off as blocks by the nepheline syenite; fine-grained gray-brown rocks occurring as dikes without well defined edges, in the nepheline syenite ; and green-black dikes of diabase or diabase porphyrite, which are latest of all, The gabbro is a speckled gray, coarse-textured rock showing plates of mica and often a few porphyritic plates of plagioclase megascopically. Thin sections are made up of half or less than half of a plagioclase having the extinction angle of andesine or sometimes labradorite; of pale bluish green augite, often idiomorphic, and brown biotite in about equal amounts, while brown hornblende and olivine are in smaller quantities. Magnetite and apatite in thick prisms are the chief accessories; and serpentine, chlorite and iron oxides occur as secondary products. In one section the biotite surrounding *Ibid., p. 5d. 154 Coleman—Nepheline and other Syenites in Ontario. a weathered olivine crystal is modified so that the parts near- est the olivine are more strongly dichroic than the rest, bright green and orange-brown in the two directions. The fine-grained dikes of brownish plagioclase rock are not very sharply defined as a rule, perhaps because they were erupted before the mass as a whole had completely cooled down. In many cases these rocks are specked with white or pale flesh-colored spots as if amygdaloidal, and they often con- tain what seem to be fragments of an older, fine-grained reddish rock. The general mass of these rocks consists of some greatly weathered, lath-shaped plagioclase, partly with a radiating arrangement, enclosing biotite, augite, and magnetite in larger amounts. In this groundmass are often well-formed crystals of augite, sometimes in groups, pale green or brown, somewhat. dichroic and with a zonal structure; and of dark brown horn- blende. The lighter patches, suggesting amygdaloids, are com- posed chiefly of plagioclase, often with well-shaped prisms projecting inwards, the center being of some transparent mineral having low double refraction, perhaps a zeolite. There are a few prisms with parallel extinction, probably nepheline, though so badly weathered as to leave their char- acter uncertain. Without an analysis it would be difficult to place this rock with certainty, so for the present it will be left unnamed. The dikes of dark gray or black diabase and diabase porphy- rite have been little studied. The only one of which thin sections have been made is an olivine diabase with compara- tively little angite, often in slender fibers or prisms having the usual extinction angle, but sometimes as broader portions between feldspar laths. The magnetite, too, has elongated rod- like forms, and when the numerous needles of apatite are included, there is evident a tendency to elongation in almost all the constituents of the rock. The large well-formed crys- tals of olivine, still fairly fresh, are, however, an exception to the rule just mentioned. These quite fresh rocks are probably of Keweenawan age like most of the diabase dikes on the north shore of Lake Superior, while the other eruptives described appear to be older, though not so old as the Huronian schists _which they penetrate. It is believed that with the possible exception of the gabbros, which may be older than the syenites, and the diabases which are distinctly younger, all the rocks which have been referred to belong to the same magma and represent phases of differ- entiation. The dikes of heronite or analcite tinguaite, though found several miles to the east of the nearest syenite, are to be looked on, no doubt, as split off from the large mass described. Coleman—Nepheline and other Syenites in Ontario. 155 The older nepheline or elaeolite rocks and their associates ean no longer be considered rare. In the province of Ontario they are known to occur very widely spread in Dungannon and adjoining townships, where they were first noticed by Dr. Adams, and where they have been followed up for many miles by Professor Miller because of their connection with the corundum-bearing band of the Laurentian. The series of eruptives described in this paper form another large mass of nepheline syenites and related rocks, though of a very different type; and the malignites described by Dr. Lawson from Poohbah Lake, west of Lake Superior, make a third, each with ite own peculiarities differing markedly from the others. The nepheline rocks of Montreal make another Canadian locality, though on a small scale, and with their alndite dikes, as described by Dr. Adams, present still another type; the whole illustrating strikingly the great variability of this group of pintonic and dike rocks as contrasted with most others. To refer to the areas described in the United States by Pirsson, Washington, Osann and others, would lead too far; and a mere list of the localities in Europe, India, South America, etc., would require considerable space. In coneluding this notice of the Port Coldwell and Penin- sula syenitie rocks, it should be mentioned that a number of them are handsome ornamental stones, as proved by polished specimens prepared by the Bureau of Mines for the Buffalo Exposition, where they attracted considerable attention. The dark gray augite syenite with its gleams of blue from the feldspars is a particularly fine stone, resembling the famous Norwegian syenite though on the whole finer in grain. As it can be obtained close to the Canadian Pacific railway and beside an excellent harbor on Lake Superior, in quarries afford- ing blocks of almost any required dimensions, it should prove of importance in the future. Toronto University, Toronto, Ontario, Canada. 156 Austin—Double Ammonium Phosphates in Analysis. Art. XIX.—The Double Ammonium Phosphates in Analy- sis; by Marta AUSTIN. [Contributions from the Kent Chemical Laboratory of Yale University—CIX.] THE function of ammonium salts in the formation of double ammonium phosphates for the purposes of analysis has been the subject of a good deal of study. Manganese, which tends to fall as the tribasic phosphate, Mn,P,O,,* appears in the presence of a sufficiency of ammonium salt in the form of the ammonium manganese phosphate (NH,)MnPO,, which gives the pyrophosphate, Mn,P,O,, on ignition. Magnesium,t on the other hand, tends to pass under the influence of ammonium salt toward the condition of the diammonium magnesium phos- phate which yields the metaphosphate on ignition. Further, in the cases of zine and cadmiumtf it has been my experience that the presence of a considerable amount of ammonium salt is essential to the precipitation of the ideal double ammonium phosphates of both these elements, although in the case of cad- mium, too large an amount of the ammonium salt prevents complete precipitation and apparently occasions the formation of a phosphate too rich in ammonia. The solvent effect of the reagents in the case of mercury phosphatet is very great, © yielding a new salt the composition of which has not been investigated in recent years. Beryllium§ is only partly con- verted to that ammonium beryllium phosphate which yields the pyrophosphate on ignition, even in the presence of large amounts of ammonia salt. Neither an ammonium salt nor ammonia in solution converts the phosphates of barinm, stron- tium, and calcium to the double ammonium phosphates. Of these three elements barium alone falls in the form of the hydrogen barium orthophosphate. In certain recent articles upon the precipitation of the double ammonium phosphates some of the facts mentioned above have been called in question. In the determination of zinc and manganese Dakin|| has pro- posed to substitute ammonium phosphate as the precipitant in place of microcosmic salt (hydrogen ammonium sodium phos- _ phate) in presence of a considerable amount of ammonium chloride, and to wash with a one per cent solution of the pre- cipitant followed by alcohol. Dakin’s analytical results, taken without scrutiny, would seem to show that the precipitate pro- * Gooch and Austin, this Journal, vi, 233. + Gooch and Austin, this Journal, vii, 187. Neubauer, Zeitschr. anorg. Chem., ii, 45-50; iv, 251-266; x, 60-65; Zeitschr. angew. Chem., 1896, 435-440 ; Jour. Am. Chem. Soc., xvi, 289. t Austin, this Journal, viii, 206. S$ Roessler, Zeitschr. anal. Chem., xvii, 148. | Chem, News, Ixxxii, 101; Ixxxiii, 37. Austin— Double Ammonium Phosphates in Analysis. 157 duced by ammonium phosphate (in only moderate excess) and washed with a one per cent solution of the precipitant and alco- hol has the ideal constitution of the double phosphate and leaves upon ignition the pyrophosphate. From the standpoint of theory it is difficult to see why the ammonium phosphate should be more effective in producing the normal ammonium double salt than is hydrogen ammonium sodium phosphate in amount sufficient to supply the ammo- nium equivalent, or than a mixture of the equivalent amount of any soluble phosphate in association with énough ammonium salt to supply the same amount of the ammonium radical or ion. Whether the conversion of the tribasic phosphate of the type R a, O, to the double ammonium phosphate of the type (NH )RPO, be viewed either as ‘dependent upon the inter- action according to mass of reagents assembled, or from the point of view of the ion theory, the action of a solution of ammonium phosphate should not differ much from that of equivalent amounts of other ammonium salt and soluble phos- phate. My own experience with the double ammonium zinc phosphate confirms this view.t In the following table are reproduced from my former paper the data of certain experi- ments bearing upon this point. Zn2P20;, corre- Error in Error Zine Time sponding terms interms left of to ZnSQOx,. of of in the stand- Taken. Found. Zn.P.0;. Zinc. filtrate. (NH,);PO,. NH,Cl. ing. erm. grim. grm. germ. erm, erm. grm. hours. A (1) 0°6355 0°6206 0°0149— 0°0060— __ trace 3°13 x. pe 14 (2) 0°63855 0°6254 0:0101— 00040-— trace 3°13 bg es 16 (3) 0°6355 0°6800 0°0055— 0:0022— __ trace 3°13 es ae 16 B HNaNH,PO, .4H.0 erm. (4) 0°68355 0°6271 0:0084— 0:0034— ~— trace 4°47 0°5 1 (5) 0'6355 0°6256 0°0099— 0:0040— none 4°47 0°5 20 C (9) 0°6855 0°6335 0:0020— 0:0008— none 4°47 10 16 (10) 0°6855 0°6381 0°-0026+ 0:0010+ none 4:47 20 4 (11) 0°6355 0°6379 0°:0024+ 0:0009+ none 4:47 20 2 (12) 0°6855 0°6886 0°0031+ 0:0012+ none 4:47 20 4 (18) 0°6355 0°63893 0:00388+ 0:0014+ none 4°47 20 $ (14) 0°6367 0°6355 0-0012+ 0°0005+ none 4°47 30 16 *Gooch and Austin, this Journal, vi, 233; Boettger, Ber. Chem. Gesell., Xxxiii, 1019. + This Journal, viii, 210. Am. Jour. Sci.—FourtH SERIES, Vou. XIV, ll No. 80.—Avu6usT, 1902. 158 Austin— Double Ammonium Phosphates in Analysis. The results of the experiments of Section B, in which the precipitation was made by microcosmic salt in presence of a small amount of ammonium chloride, show an average consti- tution of the precipitate similar to that of the precipitate obtained in A by an equivalent amount of ammonium phos- phate, but the results of both series, A and B, vary considerably from the ideal much more closely approximated in the experi- ments of O, in which precipitation was made in the presence of a large excess of ammonium chloride. With these results those of Dakin are not in accord. Upon examination, how- ever, Dakin’s procedure appears to be open to criticism. In the first place, it appears that the asbestos employed by Dakin was of the hydrous (serpentine) variety, which disinte- grates when heated and is readily acted on by many reagents. Though previously treated with hydrochloric acid, it was, by Dakin’s account, perceptibly soluble in a solution of ammonium phosphate. After drying at 100°-105° the crucible and felt lost some decimilligrams on ignition. It was on this account that Dakin weighed precipitate and filter, after drying at 100°— 105°, when the double phosphate was to be estimated as such, or after ignition when the zinc pyrophosphate was weighed, and then, dissolving the precipitate in nitric acid, reweighed the crucible and asbestos, and by difference from the former weight obtained the apparent weight of the precipitate. The inevitable loss through disintegration or solubility of the filter in the nitric acid used to dissolve the precipitate in Dakin’s procedure, must raise the corresponding apparent weight of the precipitate itself. Any series of results based upon the © use of such material must of necessity be imperfect to the extent to which the ignited filter disintegrates or dissolves under the action of the nitric acid used to dissolve the precipi- tate. Anhydrous (amphibole) asbestos, the material of which I made use, is insoluble, under the conditions of analytical work, in ordinary reagents including even the strong acids, as has been abundantly shown.* It is likewise completely insoluble in ammonium phosphate under the conditions of the work described, as I have found by experiment. Herein lies one cause of difference between Dakin’s results and mine. A second source of error in Dakin’s procedure is found in the fact that precipitates of the double ammonium phos- phates are washed in a one per cent solution of the reagent, ammonium phosphate followed by “redistilled alcohol.” Dakin calls attention to the fact that absolute alcohol must not be * Gooch, Am. Chem. Jour. i, 317. Mar, this Journal, xii, 288; xliii, 521. Browning, this Journal, xliv, 399. Phinney, this Journal, xlv, 468. Austin—Double Ammonium Phosphates in Analysis. 159 used, but makes no mention of the exact strength of the alcohol employed in his work. In order to test the insolubility of ammonium phosphate in alcoholic washing [ have made various experiments, the details of some of which are given in the following account. Portions of a solution of manganous chloride, standardized as the sul- phate according to the method* described in a former paper, were carefully measured from a burette, ammonium chloride and microcosmic salt were added in the proportions formerly recommended, and precipitation of the ammonium manganese phosphate was completed exactly as directed. After cooling, the precipitates were collected on asbestos under pressure in a perforated platinum crucible. In the experiments the results of which are given under A of the table, the precipitate was in each case washed with distilled water made faintly ammoni- acal, while in those recorded under B, C, and D of the table the precipitate was washed with two hundred cubic centi- meters of a one per cent ammonium phosphate solution, and rinsed with forty cubic centimeters of alcohol of different strengths,—sixty, eighty and eighty-eight per cent,—applied in successive portions. Mn.P.0, Washed with Washed with Washed with correspond- Washed with 1%H(NH,)2PO, 1%H(NH,)2PO, 1%H(NH,),PO, ing to ammoniacal rinsed with rinsed with rinsed with MnCl, water. 60% alcohol. 80% alcohol. 88% alcohol. taken. A B C D germ. erm. erm. erm. erm. 0°3020 0°3042 0°3050 0°3058 0°3066 0°3020 0°3041 0°3074 0°3086 From these experiments it appears that the procedure involving the washing of a precipitate of ammonium manga- nese phosphate by a one per cent solution of ammonium phos- phate, draining with the pump, and then completing the washing with alcohol, results in a contamination of the pre- cipitate proportionate to the strength of the alcohol used. Even the thin felt of asbestos alone when washed with ammonium phosphate followed by alcohol retains amounts of Weight of asbestos felt after washing ten times with a 1Z solution of am- Weight of asbestos felt after washing monium phosphate with a 1% solution of ammonium Weight of and rinsing with phosphate and rinsing with alcohol asbestos felt. distilled water. of the strength given. 60% 80% 88% germ. grm. erm. erm. erm. 0°0681 0°0681 0°0682 0°0684 0°0686 * This Journal, v, 209. 160 admitted to pass by exceptional tendencies to other forms ordinarily distinguished by marked charac- teristics. The American representatives of § Costatue, Betula nigra, B. lenta, and B. lutea, are represented by related species in Asia, but none of these trees are of very boreal range, and they appear well distinguished as endemic species. * B. pubescens [alba] x humilis, Warnst. Verh. Bot. Ver. Brandenb. xi, 129 (1870). B. nana x verrucosa [pendula], Sael. Medd. Soc. Faun. et. Fl. Fenn. xiii, 256 (1886). B. nana x pubescens [alba], Koehne, Deutsche Dendr. 112 (1893). B. pumila x lenta, Jack, Gard. and For. viii, 243, fig. 36 (1895). 190 Fernald--Lelationships of some American The American forms of §§ Albae and MNanae now recog- nized by the writer and discussed in the preceding notes may be briefly enumerated as follows: B. arpa, L. Sp. 11, 982 (1753); Roth, Fl. Germ. i, 404. B. papyrifera, Marshall, Arbust. Am. 19 (1785). B. papyracea, Ait. Hort. Kew. in, 337 (1789). .B. pubescens, Ebrh. Beitr. v, 160, vi, 98 (1790-91). B. odorata, Bechst. Diana, i, 74 (1797).— NeEwFounpDianp to ALasKa, south to Pennsytvanta, INDIANA, Nerpsraska, Wyomine, Ipano and WasuineTon ; passing on the Pacific coast to the dark-barked forma occidentalis (B. occidentalis, Hook. Fl. Bor.-Am. ii, 155 (1839)); IceLann, northern Evropr and Asta, south in the mountains to northern Spain, Iraty, ete. (Pl. V, figs. 1-6.) B. ALBA, var. GLUTINOosA, Trautv. ex Regel, Mon. Bet. 20 (1861). B. glutinosa, Wallr. Sched. Crit. 497 (1822). JB. pendula, Reichenb. Ic. Fl. Germ. xu, t. 625, not Roth.— Valley of Wassataquoik River, Marinz; Swepen, Finuanp, GERMANY, SWITZERLAND, AUSTRIA. B. auBa, var. corpirotia. LB. cordifolia, Regel, Mon. Bet. 28, t. 12, figs. 29-386 (1861). BL. alba, subsp. papyrifera, B, cordifolia, Regel in DC. Prodr., xvi, pt. i, 166 (1864). B. pupyriferd, var. minor, Wats. and Coult. in Gray, Man. ed. 6, 472 (1889), in part, not B. papyracea. var. minor, Tuck.— Lasrapor and Nrwrounpnanp to New Brunswicx, Mains, New Hampsuire, Lake Superior, lowa, ALBERTA, BrRitisH CotumetiA, Ipano, and WAsHINGTON. _ B. avpa, var. minor. B. davurica, Ledeb., Fl. Alt. iv, 245 (1833), not Pallas. LB. papyracea, var. minor, Tuckerman, this Journal, xlv, 31 (1848). B. tortwosa, Ledeb., Fl. Ross. iii, 652 (1849). B. edorata, var. alpigena, Blytt, Norg. Fl. 402 (1861). &. alba, subsp. tortuosa, Regel, in DCS iter aiae (1864). B. davurica, B, americana, Regel, |. c. 175 (1864). B. odorata, var. tortuosa, Lange, Fl. Dan. xvu, 10, t. 2918 (1877). B. papyrifera, var. minor, Wats. and Coult. 1. ¢., in part. BL. pubescens, var. tortuosa, Koehne, Deutsche Dendr. 109 (1893).—Laxsrapor to the mountains of Mainz, New HamrsHire and ‘VERMONT; mountains of SASKATCHEWAN, Asstntpora, and ALBERTA; GREENLAND, IckLAND, LAPLAND, Finan, northern Germany, Attar Mrs.; dwarf forms from Auaska resemble this variety, but have the strongly resini- ferous branchlets of B. glandulosa and B. pendula. (Pl. V, figs. 7-12.) Betula ALBA, var. carPATIcA. LB. carpatica, Wald. and Kit. in Willd. Sp. iv, 464 (1805). B. borealis, Spach, Ann. Sci. Nat., ser. 2, xv, 196 (1841). B. glutinosa, Fries, Summ. Veg. Seand., 212 (1846), not Wallr. &B. pumila, y, borealis, Regel, Mon. Bet. 55, t. 18, figs. 38, 39 (1861). B. alba, subsp. ~~. ps eae weet. 2) Per and Old World Birches. 191 pubescens, [ car "‘patica, Regel in DC., 1. c. 168 (1864). B. odorata, var. carpatica, Lange, Haandb., ed. 3, 708 (1864). vif odorata, var. rhombifolia, Lange, Fl. Dan., xvi, t. 2851 (187 1).— Anticosti, Quesec; ALBertTa; and northward; Scay- DINAVIA to Germany, Austria and Russia. (PI. V, figs. 13-14.) B. penpura, Roth, Fl. Germ. i, 405 (1788). B. verrucosa, Ebrh., Beitr. vi, 98 (1791). B. alba, var. verrucosa, Wallr., Sched. Crit., 495 (1822). B. alba, var. vulgaris, Spach, 1. ¢. 186 (1841). B. odorata, Reichenb., Te. Fl. Germ., xii, fig. 1288 (1850), not Bechst. JB. gunmifera, Bertol., Fl. It., x, 229 (1854). B. alba, subsp. verrucosa, a, vulgaris and 6, resin- ifera (in part), Regel ; in DC., 1. c. 163, 164 (1864). B. kenaica, W. H. Evans, Bot. Gaz., xxvii, 481 (1899), in part. B. alas- kana, Sargent, Bot. Gaz., xxxi, 236 (1901), mostly —QuvEBEc to Inirots, ALBerTA, Mackenzie and Ataska; Europe and Asia, widely distributed. (Pl. V, figs. 15-18; Pl. VI, figs. 19-22.) B. PENDULA, Var. JAPONICA, Rehder in Bailey, Cyc. Aan. Hort., i, 159 (1900). B. japonica, Siebold, Verh. Batay. Gen. xl, 25 (1830). B. latifolia, Tausch, FI. Ratisb., 751 (1838). Bs “alba, subsp. verrucosa, 8 resinifera, Regel in DC., |. ¢. 164, in part; subsp. mandshurica and latifolia, Regel, 1. ¢. 165 (1864). B. kenaica, W. H. Evans, 1. c. (1899), mostly. B. alaskana, Sargent, |. c. (1901), in part.—Sunearia to Japan, north to the Yenisei River, Srperta, and KamrscHatTKa ; east to Peel River and Fort Simpson, Mackenzie, and along the ALASKA coast; and apparently on the coast ‘of Washington Co., Marne (trees sterile). (Pl. VI, figs. 23, 24.) B. POPULIFOLIA, Marshall, Arbust. Am. ,19 yar: B. alba, var. populifolia, Spach, Ann. Sci. Nat., ser. 2, xv, 187 (1841). B. alba, subsp. populifolia, Regel, in DC., 1. ¢. 164 (1864).— Prince Epwarp Isianp to central Marne, southwestern QUE- BEC, and western New Yorx, south mostly on the coastal plain to DELAWARE. : B. MicropaHyiia, Bunge, St. Pétersb. Mém. Savans Etrang., ii (1835), 606-—reprint, Fl. Alt. Suppl. 84. B. occedentalis, Nutt., Sylva, i, 22, t. 7 (1842), not Hook. B. rhombifolia, Nutt., 1. ¢. 24, t. 8, not Tausch. B. fruticosa, var. cuneifolia, . Regel, Mon. Bet. (1861) 35, t. 7, tigs. 16-23. _B. alba. subsp. soongorica, Regel, Bull. Soe. Imp. Nat. Mose., vi, (1868)— reprint, Enum. Pl. Semenow (1869) 99. B. fontinalis, Sar- gent, Bot. Gaz. xxxi, 23 (1901)—-In the mountains from Aaska to northern CaLIFornta, SASKATCHEWAN, SoutH Da- Kota, and New Mexico; Atral and Tyan SHAN Mrs., central Asia. (Pl. VI, figs. 25-32.) B. nana, L., var. Micwavxm, Regel, Mon. Bet. (1861), 45. B. Michaucii Spach, ].c.195 (1841). “Apter ocaryon Michauzis, Opiz. Lotos, v (1855), 258.—Hupson Bay, Laprapor and Newrounpianp. (PI. VI, figs. 47, 48.) 192 Fernald— Relationships of some American B. pumiva, L., Mant. 124 (1767). 2B. alpestris, Fries, Summ. Veg. Scand., i, 212 (1846). SB. fruticosa, var. humilis, Reichenb. Ie. Fl]. Germ., xii, fig. 1280 (1850). 8B. nana var. alpestris, Regel, Mon. Bet. 45 (1861). &. Grayz, Regel, Bull. Soe. Imp. Nat. Mosce., xxxviii, 406, t. 6, figs. 9-13 (1865),— Lasrapor and.NrwrounpLanp to Ontario, south to Morris Co., New Jersny, Champaign Co., Outo, Lake Co., Inprana, and McHenry Co., Intinois; GREENLAND, SCANDINAVIA, north- ern GERMANY, Fintanp, Lartanp, Russia, Srperta. (Pl. VI, figs. 33-38.) B. PUMILA, Var. GLANDULIFERA, Regel in DC., 1. c. 178 (1864). —Ontario and Micuiean to Minnesota, SaAskKATCHEWAN and British Cotumpia, south in the mountains to Ipano and OREGON. B. etanputosa, Michx., Fl. Bor.-Am., ii, 180 (1808). B. nana of various American authors, not L. £. Littelliana, Tuckerman, this Journal, xlv, 30 (1843).—GreEENLAND and Hupson Srrairs to KamtTscnatKa, and the Altai Mts. of SIBERIA; south in eastern America to the higher mountains of Marne and New Hampsuire; in the interior to LaxKsE Superior and Manrropa; and in the western mountains to SoutH Dakota, Cotorapo, Utan, and northern CALirornia. (Pl. VI, figs. 39, 40.) B. GLANDULOSA, var. ROTUNDIFOLIA, Regel in DC., 1. ¢. 172 (1864). B. rotundifolia, Spach, 1. c. 194 (1841). B. nana, var. sibirica, Ledeb., Fl. Ross., 11, 654 (1849).—GreEENLAND and northern Laprapor to KamrscHarKa, and the Altai Mts. of Stperra, south to the higher mountains of Marne and New Hampsuire, and along the coast of ALaska. Perhaps hybrid- izing with B. pendula. (Pl. VI, figs. 41-44.) tn 6 and Old World Birches. 193 EXPLANATION OF PLATES.* Puate V, figs. 1-6, BETULA ALBA. Figure 1.—Leaf of young flowering branch of B. pubescens, Ehrh., from the Vosges Mts., near Ramberviiles, France (Joad). Figure 2.—Leaf of fruiting branch of B. papyrifera, Marsh., from Lake Winnipeg, Manitoba (Bourgeau). Figure 3.—Leaf of fruiting branch of B. occidentalis, Hook., from Pend d’Oreille River, British Columbia (Lyatv). Figure 4.—Leaf of young branch of B. pubescens, Ehrh., from Bohemia (Tausch). Figure 5.—Leaf of fruiting branch of B. papyrifera, Marsh., from South- port, Maine (Fernald). FicurE 6.—Leaf of fruiting branch from Austria—after Ettingshausen and Pokorny, Phys. Pl. Aust. iii, t. 201. Puate V, figs. 7 to 12, B. ALBA, var. MINOR. Figure 7.—Leaf of fruiting branch of B. tortuosa, Ledeb., from the Altai Mts., Siberia (ex. herb. St. Petersb.). Figure 8,—Leaf of fruiting branch of B. odorata, var. tortuosa, Lange, from the Dovre Mts., Norway—after Lange, Fl. Dan. xvii, t. 2918. Ficures 9, 10.—Leaves of original fruiting branches of B. papyracea, var. : minor, Tuck., from Mt. Washington, New Hampshire. Ficure 11.—Leaf of dwarf form of B. papyracea, var. minor, Tuck., from Mt. Washington, New Hampshire (Faxon). Ficure 12.—Leaf of fruiting branch of B. odorata, var. minor, Rosenvinge in herb., from Greenland (Hartz). PuaTE V, figs. 13, 14, B. ALBA var. CARPATICA. Figure 13.—Leaf of fruiting branch of B. borealis, Spach, from Anticosti, Quebec (Macoun). Figure 14.—Leaf of B. alba, subsp. pubescens, ¢ carpatica, Regel, from Lapland (Regel). PuateE V, figs. 15 to 18, Puate VI, figs. 19 to 22, B. PENDULA. FicuRes 15, 17.—Leaves of young flowering branch of B. alba, subsp. ver- rucosa, 0 resinifera, Regel (type of B. alaskana, Sargent) from Saskatchewan (Bourgeau). Ficures 16, 18.—Leaves of fruiting branch of B. verrucosa, Ehrh., from Christiania, Norway (Blytt). Figure 19.—Leaf of fruiting branch of B. pendula, from Warren, Illinois (L. M. Umbach, sheet No. 351,017 U. S. Nat. Herb.). Figure 20.—Leaf of fruiting branch from Gotland, Sweden (Blomberg). FIGURE 21.—Leaf of B. alba, subsp. mandshurica, Regel, from Mandschuria— after the original illustration (Regel, Bull. Soc. Imp. Nat. Mosc., 1865, t. 7, fig. 15). FIGURE 22.—Leaf of fruiting branch of B. verrucosa, 6 resinifera, Regel, from Nushagak River, Yukon District, Alaska (McKay). PuaTE VI, figs. 23, 24, B. PENDULA, var. JAPONICA. Figure 23.—Leaf of B. alba, subsp. latifolia, a Tauschii, Regel, from Eastern Asia—after Regel, Bull. Soc. Imp. Nat. Mosc., 1865, t. 7, fig. 11. Figure 24.—Leaf of B. kenaica, W. H. Evans, from Cook Inlet, Alaska (Coville and Kearney, No. 2412). *The plates illustrating this paper have been carefully prepared by Mr. F. Schuyler Mathews. Unless otherwise stated, the figures are life-sized. 194. . Fernald—American and Old World Birches. PuaTE VI, figs. 25 to 32, B. MICROPHYLLA. FIGURE 20.—Leaf of young shoot of B. microphylla from the Altai Mts., Siberia (ex. herb. St. Petersberg). FicurE 26.—Leaf of B. fruticosa, var. cuneifolia, Regel (syn. B. microphylla, Bunge) from the Altai Mts., Siberia—after Regel, Mon. Bet. (1861) tii, eS: FIGURE 27.—Leaf of fruiting branch of B. occidentalis, Nutt. (B. fontinalis, Sargent) from Idaho Springs, Colorado (Engelmann). FIGURE 28.—Small leaf from fruiting branch of B. occidentalis, Nutt. (B. fontinalis, Sargent) from Coulee City, Washington (Lake and Hull, No. 790). FIGURE 29.—Leaf of young shoot of B. occidentalis, Nutt. (B. fontinalis, Sargent) from the Black Hills, South Dakota (Rydberg, No. 1006). Figure 30.—Leaf of fruiting branch of original material of B. alba, subsp. soongorica, 8 microphylla, Regel, from the Tyan Shan Mts.,. Central Asia (Semenow). Figures 31, 32.—Leaves of fruiting branch of B. occidentalis, Nutt. (B. fontinalis, Sargent) from Laramie Peak, Wyoming (A. Nelson, No. 1647). Puate VI, figs. 33 to 38, B. PuMILA. Ficure 33.—Leaf of sterile shoot of B. pumila from Anticosti, Quebec (Macoun). Figure 34.—Leaf of sterile shoot of B. alpestris, Fries, from Lapland (Laestadius). FiguRE 35.—Tip of branch from Bonne Espérance, Quebec (Allen, No. 70). Figure 36.—Leaves of glabrate form from Bay of Islands, N ewfoundland (Waghorne). Figure 37.—Leaves of B. alpestris, Fries, from N BE ee Lange, FI. Dan., Suppl. t. 37. Figure 38.—Leaves of young branch of B. alpestris, Fries, from Lapland (Andersson, No. 186). PuateE VI, figs. 39, 40, B. GLANDULOSA. F1GuRE 89.—Leaf of branch from Mt. Washington, New Hampshire (J. A. Allen). Figure 40.—Leaves of branch from Hopedale, Labrador (Sornborger, No. 80). PuatE VI, figs. 41 to 44, B. GLANDULOSA, var. ROTUNDIFOLIA. Ficure 41.—Leaf from Mt. Washington, New Hampshire. Ficures 42, 48.—Leaves from Nunivak Island, Behring Sea (J. M. Macown). Ficure 44.—Leaf from the Altai Mts., Siberia (ex. herb. St. Petersb.). PuaTE VI, figs. 45, 46, B. Nana. Figure 45.—Fruiting branch from Grenjadastad, Iceland (Elizabeth Taylor). Figure 46.—Scale from same, enlarged three times. PuatE VI, figs. 47, 48, B. nana, var. MICHAUXII. Ficure 47.—Fruiting branch from Grand Lake, Newfoundland (Waghorne). Ficure 48.—Scale from same, enlarged three times. Plate VI. Am. Jour. Sci., Vol. XIV, 1902. 21 a 19 22 Sellards—Fronds of Crossotheca and Myriotheca. 195 Art. XXII.— On the Fertile Fronds of Crossotheca and Myrio- theca, and on the Spores of other Carboniferous Ferns, From Mazon Creek, Illinois; by E. H. SELLARDS. (With Plate VII.) INFORMATION in regard to the spore-bearing organs of Car- boniferous ferns has accumulated slowly and with difficulty. The parts of the plants are usually disconnected, and more or less fragmentary. Dimorphic genera are not uncommon, and specimens connecting the fertile and sterile segments or fronds are rare. It is usually difficult to correlate genera described from microscopic structure with others based on plant impres- sions. And yet, a satisfactory knowledge of a considerable number of genera and species has resulted from the work of the various investigators who have taken up this subject since the time of Brongniart. These investigations indicate that ferns with the annulus absent or but slightly developed, and having other Marattiaceous characters, predominated in the Carboniferous, and included a much greater range of form and structure than is seen in the living representatives of the family. Besides the numerous exannulate ferns, others are known with a well-developed annulus, and are, therefore, pre- sumably Leptosporangiate. The reference of these fossils to their respective families of living ferns is attended with more or less doubt. The Hymenophyllacez, Gleicheniaces, Schize- acese, and Osmundacez have been recognized with some degree of certainty. Prof. Renault, of the Museum of Natural History of Paris, has recently described Parkeriordea Renault, a genus from the Coal Measures of Grand’ Croix, near St. Etienne. The char- acter of the annulus, the form of the spores, and the ornamen- tation of the exospore have led him to refer this form to the Parkeriaceze. Certain of the spores show sculpturing, while others are smooth and have three radiating lines at the apex. The former are interpreted as microspores, the latter as mega- spores.” The same writer had previously detected what he believed to be indications of heterospory in Pecopteris, one of the Marattiaceous ferns,t as well as in an extinct family of ferns, the Botryopterides.{t The evidence of heterospory in the Botryopterideze has not been fully accepted. The papers on Pecopteris and Parkerioidea are mentioned more fully later in the present article, where, in connection with the descrip- * Comptes Rendus de l’Academie des Sciences, March 10, 1891. + Ibid., October 21, 1891. t Bull. Soc. Hist. Nat., Autun. , iv, 1891. §See Seott, Studies in Fossil Botany, p. 289 ; Zeiller, Eléments de Paléo- botanique, p. 74. Am. Jour. Sct.—FourtTH Srrigs, Vou. XIV, No. 81.—SEPTEMBER, 1902. 196 Sellards—Lronds of Crossotheca and Myriotheca. tion of the spores of some Carboniferous ferns, it is pointed out that, as far as the radiating lines (“lines of dehiscence ”’) at the apex are concerned, they cannot be considered character- istic of megaspores. : The fructification of several genera of Carboniferous ferns is well shown in an exceptionally large and complete collec- tion from Mazon Creek, Illinois, in the Yale Museum. The sporangia are often preserved, and in many cases the spores are found in place, and can be removed and studied. In the present paper the Mazon Creek representatives of two inter- esting genera, Crossotheca and Myriotheca, will be described, together with the spores of some other species. In the earlier American literature many of the fertile ferns were grouped together without sufficient regard to their true generic separation. Sorocladus, as established by Lesquereux,* was so broadly defined as to include more than one natural genus. WS. stellatus was the first of the five species described . under the genus. Four of the species referred in the “ Coal Flora” to Sorocladus had been previously placed by Les- quereux in the Tertiary Staphylopteris Presl. It was probably Schimper’s objection to considering these forms under Presl’s genus that led Lesquereux to create aseparate genus for them.t One of the five original species of Sorocladus, S. ophioglos- soides, has been referred by David White to Crossotheca, and S. sagittatus was recognized as falling naturally within the same genus. Crossotheca. Zeiller, Ann. Sci. Nat. (Bot.), ser. 6, vol. xvi, 1888. Crossotheca is a genus of more than ordinary interest, because of its dimorphic fronds, its large marginal sporangia, and large spores. Several species are known in Europe, all of Coal — Measure and Permian age. Besides the two species just men- tioned from this country, a third is added in the present paper. Crossotheca sagittata. Plate VII, figures 1-3c, 8. Staphylopteris sagittatus Lesq., Geol. Surv. Il., vol. iv, p. 407, pl. xiv, figs. 4-6, 1870. Pecopteris abbreviata Brongn. ? Lesq., Geol. Surv. II1., vol. iv, p. 403, 1870 ; Second Geol. Surv. Penn., Description of the Coal Flora, vol. i, p. 248, pl. xlvi, figs. 4-6a, 1880. | Sorocladus sagittatus Lesq., Coal Flora, vol.i, p. 329, 1880; Atlas, pl. xlviii, figs. 10-100, 1879 ; vol. iii, p. 761, pl. C, figs. 4-5, 1884. Pecopteris Fontainei, Lesley’s Dict. of the Fossils of Penn., p. 606, 1889 text figure. See, also, Lesquereux, unpublished manuscript. * Second Geol. Surv. Penn., Description of the Coal Flora, vol. i, p. 327, 1880. + Paléont. végét., vol. iii, p. 512. tMon. U. S. Geol. Surv., No. 37, Flora of the Lower Coal Measures of Missouri, pp. 60-64, 1899. or" Sellards—Fronds of Crossotheca and Myriotheca. 197 Crossotheca sagittata preserves the details of fructification much better than the other American species, and illustrates well the characters of the genus. The large fertile pinnules are expanded at the base in the form of an arrow, thus allow- ing greater area for the attachment of the sporangia. The small pinnules are slightly or not at all enlarged at the base. The upper surface of the pinnule is flat with a distinct median line, and with the lateral veins obscured. The sporangia are unusually large, measuring 23 to 47™ in length and $ to ?™ wide. They are placed as seen in figures 1, 2, and 3, in a single row around the entire border of the pinnule, free nearly or quite to the base, and are often seen filled with spores. Figure 2 gives a side view of the pinnule as partly freed from the matrix, and showing the full length of the sporangia. From a study of the type of the genus, Prof. Zeiller thought it probable that the sporangia were united in little clusters at the ends of the nerves. The specimens figured and others in the Yale collection indicate that in the case of C. sagittata, at least, the sporangia. are attached side by side in a single row, without any tendency toward grouping. The same specimens confirm the statements of Zeiller that these are individual spo- rangia, since, in the specimens at hand, they are often filled with spores, in contradistinction to Stur’s interpretation of the fringed pinnules as dehisced sporocarps.* Some of the best preserved sporangia show a slit on the outer side, as seen in figure 3a, which probably indicates the place of dehiscence. The sterile part of the frond is very different from oe fer- tile, so much so that if not found in direct connection their relation would hardly be suspected. The pinnules are small, rounded, close, oblique, connate, and decurrent at the base, the smaller entire, the larger becoming lobate. The ultimate pinnee are broadly linear-lanceolate, alternate, oblique, and close, often touching. The rachis is large and round. The midrib of the pinnule-is broad, shallow, and decurrent. The lateral veins curve regularly to the border, and fork once, twice, or three times, according to the size of the pinnule. The surface i is rough, appearing “minutely scaly. Some of the veins are heavier than others, giving the venation an irregular appearance. The extreme apex of the frond is often sterile, the fertile pinnules and pinne appearing at some distance below. This is not always the case, however, since in the frond figured. by Lesquereux (“ Coal Flora, ” volume i iil, pl. C, figure 4) the entire apical part is fertile. It is not possible to state, on any evi- * Abhandl. d. k. k. Geol. Reichsanstalt, Wien, 1885-87, Flora der Schatz- laren Schichten, Part I, pp. 273-275. aa fee 198 Sellards—Fronds of Crossotheca and Myriotheca. dence at hand, whether the entire frond below the apex was fertile, or only a few of its segments. There is no indication of sterile segments below the fertile ones, although some of the incomplete fronds reach a length of 15 or 16. It is prob- able that some of the fronds were entirely sterile, and that others were mostly sporangia-bearing, the apical part only being, in most cases, sterile. The spores of this species are large, from *056 to :060™™, round, and marked at the apex by three distinct radiating lines. The exospore is thick, resistant, brownish, and marked by minute warty thickenings. The sterile fronds were at first doubtfully referred by Les- quereux in the “ Coal Flora” to Pecopteris abbreviata Brongn.* In volume ili of the same work, however, a small part of the sterile apex is figured in connection with the fertile frond, and David White states that Lesquereux’s unpublished manuscript © contains descriptions and figures of the two parts in connec- tion.t In the Yale collection the fertile and sterile parts are shown in direct connection in no less than nine instances. (See figure 8.) Crossotheca trisecta sp. 0. PuatE VII, figures 44c, 9. A second and apparently new species is present in the mate- rial from Mazon Creek. The sterile part of the frond is much like that of C. sagittata, but the fertile pinnules are entirely different. The latter are usually trisectate. The central lobe is elongate-ovate, or nearly round, and borne at the end of a slender stalk. The lateral lobes are smaller, round, and borne on short lateral stalks. A second pair is sometimes borne by the larger pinnules. Lateral lobes may be lacking in one or two pinnules near the apex of the pinna. The sporangia are probably smaller than those of C. sagittata, and are not dis- tinctly preserved on either of the two fertile fronds in the present collection. The sporangia-bearing lobes have a form much like that of the type of the genus C. Crépinz, but the type species lacks the trilobate appearance of the pinnules, and has more finely divided sterile fronds having a different type of venation.t C. ophioglossoides from Clinton, Missouri, has narrower and longer fertile pinnules. The lines on the upper surface of the pinnule, present on other species of the genus, are much more distinct than on C. * Second Geol. Sury. of Penn., Description of the Coal Flora, vol. i, p. 248; Atlas, pl. 46, figs. 4-6, 1880. + Mr. White informs the writer that the name Pecopteris Fontainet, sp. novy., is given to the sterile fronds of this species in Lesquereux’s manuscript. t See the figures of C. Crépini given by Zeiller, Ann. Sci. Nat. (Bot.), ser. 6, vol. xvi, 1888, and by Stur under the name of Sorotheca Crépini, Flora der Schatzlaren Schichten, pl. xxxv, figs. 3, 4. Sellards—Lronds of Crossotheca and Myriotheca. 199 sagittata, and sometimes branch. The figured specimen is 15™ long; the first 5 or 6™ are sterile, the remaining pinne being partly or entirely fertile. When detached and in fragments the sterile part of the frond is distinguished with difficulty from that of C. sagittata. The pinnules are perhaps more finely lobate. The spores are smaller than those of C. sagitéata, measuring from -030 to :036™". They are somewhat triangular, with a smooth, thin exospore. The name Crossotheca trisecta is suggested for the species. | Myriotheca. Zeiller, Ann. Sci. Nat. (Bot.), ser. 6, vol. xvi, 1883. Myriotheca has numerous independent, sessile, round or ege-shaped sporangia, covering the entire lower surface of the pinnule. The genus is represented at Mazon Creek by a single species, which apparently is the fern described by Lesquereux from Morris, Ill., as Sphenopteris scaberrima,* although the rachis is smooth or striate, not punctate as given for that species. The round sporangia are very numerous, close, or almost contiguous, half immersed in the leaf substance, and cover the entire lower surface without any kind of regularity of arrangement or grouping. The spores are of medium size, measuring from °036 to -040™", triangular, with the sides some- times slightly concave. The genus is a rare one both in Europe and in America. No other species has been reported from this country. The genus was founded by Zeiiler on a single fragment from the. Coal Measures of France. The European specimen representing the type species, JZ. Desazllyi, has smaller pinnules with a tendency to become lobate. The sporangia of the American species are nearly round, and larger than those of the European species, measuring ‘40 to *50™™. Because of the absence of any indication of an annulus, Prof. Zeiller included both Crossotheca and Myriotheca with the Marattiaceze. The large size of the spores and comparatively small output to the sporangium are, however, characters not met with in the living representatives of that group. The position of the sporangia, marginal in Crossotheca, and cover- ing the whole lower surface of Myriotheca, is unusual for Marattiaceous ferns. Spores of other Ferns from the same Locality. At least four other species of ferns in the Yale collection have the spores preserved. All retain their natural brown color, and something of their food contents, and, as far as appearances are concerned, might be spores from living plants. * Geol. Surv. of Illinois, vol. iv, p. 408, pl. xv, figs. 1 and 2, 1870. 200 Sellards—Lronds of Crossotheca and. Myriotheca. Some of the larger spores have granular bodies within or cling- ing to them, which show a dark spot at the center and some- thing of the structure of concentric starch grains. The spores from a large number of fronds of two species have been examined in order to find whether or not there were indications of more than one kind of spores. The species studied were Pecopteris (Ptychocarpus) unita Brongn., and the form referred doubtfully by Lesquereux to P. villosa Brongn.,* which probably belongs to the Asterotheca division of Pecopteris. Both species are extremely abundant at Mazon Creek, and the sporangia-bearing fronds numerous. The spores of P. villosa are small, measuring only -013 to -016"", smooth and spherical. The exospore is very thin. The spores of the European examples of P. unita have already been made known by Renault.t The spores of the specimens at hand are ‘016 to -018™" long, and -010 to ‘011 wide, being elongate or bean-shaped when seen from the side. The exospore is thick and smooth. The three radiating lines at the apex can be seen on some spores. As in other Marattiaceous ferns, the spore output to the sporangium in both species was evidently very great. The spores from many specimens of both species and from various parts of the same specimen present no differences in structure, size, or sculpturing, that could be interpreted as indicating two kinds of spores. It is, therefore, practically certain that both were homosporous, and this is exactly what might be expected in typically Marattiaceous ferns. The fact is of interest in connection with Renault’s paper referred to above, in which unusual conditions ‘are observed in one of the European species of Pecopteris. The fern described by Renault, which is of the Asterotheca division or sub-genus of Pecopteris, has one set of spores which are smooth and marked at the apex by three radiating lines. These are considered megaspores. In the same sorus, and possibly in the same spo- rangium, are other spores of about the same size, thought to be microspores, which lack the lines at the apex and show struc- tures interpreted as the mother cells of antherozoids. The second paper by the same author describes somewhat similar appearances in Parkerioidea. The megaspores are smooth and show the triradiate lines at the apex. The micro- spores, found in the same sporangium, lack the lines, and are sculptured with a polygonal network. The three radiating lines are seen on the spores of all the ferns examined by the writer, when viewed from the apex, and * According to Mr. Robert Kidston, Fossil Flora of the Radstock Series, Trans. Roy. Soe. Edinburgh, vol. XXxili, Part II, 1886-7, p. 37, P. villosa has a doubtful existence, having "been established in all probability on a villous specimen of P. oreopteridia or a Closely related species. + Bassin Houiller et Permien d’Autun et d’Epinoe, Pt. II, p. 10. Sellards—Fronds of Orossotheca and Myriotheca. 201 on both micro- and megaspores of Selaginella, and the Car- boniferous Lycopods, as well as on such heterosporous living -ferns as Marsilea. The tetrahedral division of the spore mother cell, of which the three radiating lines are indicative, is well _known to be extremely constant, not only for the Pterido- phytes, but for all those plants commonly grouped under the Archegoniatez, and for the microspores of most of the flower- ing plants.* The lines, therefore, cannot be considered characteristic of, or in any way distinguishing megaspores. Their absence in some cases may be due to imperfect preservation, or they may be obscured by the view of the spore presented. In the case of Parkerioidea, there is some doubt as to whether it is not possible that the spores when seen from the apex present the Jines and a smooth face, and when seen from the base are sculp- tured, the lines being obscured by the thickness of the spore. The recent studies of Prof. Bowert have directed attention to the importance of the size of the spores and the number to the sporangium. Bower’s investigations show that among liv- ing ferns an increase in the size of the spores, correlated with a decrease in the output to the sporangium, accompanies, in a general way, the advance in development and specialization from the Marattiacesze through the various families of the Leptosporangiate ferns. The little that is definitely known of the spores of fossil ferns supports Bower’s conclusions. It isa question, however, how far the size and number of the spores may be relied upon to separate Marattiaceous from non-Marat- tiaceous ferns. The spores of Pecopteris villosa are smaller than those of such living Marattiacezee as Angiopteris evecta, Kaulfussia, Marattia Douglassii, or Danea moritziana. Crossotheca and Myriotheca have much larger spores, comparable in size to many of the Leptosporangiate ferns. It is hardly possible, with fossil ferns, to count the number of spores to the spo- rangium, but it is evident that in the case of Pecopteris unita and P. villosa, the output to the sporangium was very great, yee that of Crossotheca and Myriotheca was comparatively small. Geological Department, Yale University Museum. * See Campbell, University Text-book of Botany, 1902, pp. 199 and 323. + Studies in the Morphology of Spore-Producing Members, Parts III and IV, Phil. Trans. Roy. Soc., vol. clxxxix, 1897, pp. 35-81 ; vol. excii, 1899, pp. 29-138. 202 Sellards—Fronds of Crossotheca and Myriotheca. EXPLANATION OF PLATE VII. Figure 1.—Crossotheca sagittata ; part of a fertile frond. The lower and the upper pinnules on the right hand side show the expanded base. The second pinnule from the base on the same side gives the full length of the sporangia. x11. FIGURE 2.—Same species ; a pinnule with the matrix removed to show the full length of the sporangia. x 2. FIGURE 3.—Same species; a medium sized pinnule seen from the base and side. x2, FIGURE 38a.—A single sporangium. x4. FIGURE 3b.—Spores of the same species. x 240. FIGURE 3c.—Cross section of a fertile pinnule with sporangia. x 2. FIGURE 4.—Crossotheca trisecta sp. n.; fertile and sterile parts of frond. x 44. Ficuress 4a, 4b.—Fertile pinnules of C. trisecta. FicureE 4c.—Spore of C. trisecta. x 240. FIGURE 9.—Myriotheca scaberrima ; fertile pinnules. x 2. FIGURES 5a—5c.—Spores of the same species. x 240. Ficures 5d, 5e.—Starch grains from the spores of the same species. x 240. FIGURES 6a-6d.—Spores of Pecopteris villosa. x 240. FIGURE 7.—Pecopteris unita ; fertile pinna. x 2. FIGuREs 7a—7d.—Spores of the same species. x 240. FIGURE 8.—Crossotheca sagittata; fertile and sterile parts in connection. FIGURE 9.—Crossotheca trisecta; sterile pinnule. x 2. [ x14. CARBONIFEROUS FERNS. Sellards— Validity of Idiophyllum rotundifolium. 208 Art. XXILI.—On the Validity of Idiophyllum rotundifolium Lesquereux, a Fossil Plant from the Coal Measures at Mazon Creek, Illinois ; by E. H. SELLARDS. THE genus /diophyllum was proposed by Lesquereux for a species of Carboniferous plants represented by a single speci- men from Mazon Creek, Illinois.* The species /. rotundifoliwm appeared to present characters so peculiar that the genus was placed by Lesquereux in his classification with the “‘ Ferns of Uncertain Relation,” and was compared with Dictyophyllum, and with dicotyledonous leaves. Figure 1.—Obverse of the type of Idiophyllum rotundifolium Lesqx. In working over a large collection of plants from the same locality, in the Yale Museum, the writer has found the obverse side of Lesquereux’s type. The obverse (figure 1) is well pre- served, and completely demonstrates the true nature of the plant. The fossil represents the distorted apical part of a young and not fully expanded fern frond. The tip is pushed to one side, -erowding the lateral pinnz and partly obscuring the outline of the pinnules. The pinnules, however, are much more distinct than is represented in Lesquereux’s figure of the counterpart. They are 6 to 10™™ in length, 3 to 34™" in width, alternate, obtuse, and somewhat cordate at the basal attachment. The rachis is longitudinally striate; the lateral pinnz are close, oblique, and alternate. In all these characters /diophyllum rotundifolium agrees with Neuropteris rarinervis Bunb., a * Second Geol. Surv. Penn., Description of the Coal Flora, vol. i, p. 159 ; Atlas, pl. xxiii, fig. 11, 1880. 204 Sellards— Validity of Idiophyllim rotundifolium. species common at the locality. The outline and cordate base of the pinnules, and especially the faint indication of lobation of the upper border, just above the base (figure 2), are characters of LV. rarinervis. Although the lateral nervation is mostly obscured, there can be little doubt regarding the specific iden- tity. The lateral venation shown in figure 2 is taken from several pinnules. The lateral pinnze are somewhat more crowded than is usual for JV. rarinervis, a condition explained by the immaturity of the frond. The plant is a difficult object: to photograph, but the figure here given will perhaps help to clear up some of the peculiarities attributed to the fossil. The appearance of nerves “sometimes crossing each other in con- trary directions and forming by intervention regular quadrate or rhomboidal meshes ” is caused by the crowding and overlap- ping of the pinnules. : FIGURE 2.—A single pinnule ; showing the characters of Neuropteris rari- nervis Bunb. ; taken from the right side of the specimen. x2. Altogether, it seems evident that the species Jdiophyllum rotundifolium is a synonym of WVeuropteris rarmervis, and that the genus Jdiophyllum has no status in systematic fossil botany. Phidach the courtesy of Mr. David White, the writer has recently had an opportunity of examining the type of Jdzo- phyllum rotundifolium, now in the Lacoe Collection of the United States National Museum. The plant is not entirely freed from the matrix, the tips of the lateral pinnez on the right side and at the top being still partly covered. Mr. White had also recognized that the fossil represents an imma- ture frond, and agrees with the writer that it is Wewroptercs ravrinervis. | Yale University Museum, Geological Department. Gooch and Gilbert—Ammonium Vanadate. 205 Art. XXIV.—The Precipitation of Ammonium Vanadate by Ammonium Chloride; by F. A. GoocH and R: D. GILBERT. {Contributions from the Kent Ghemical Laboratory of Yale University—CX.] BERZELIUS was the first to point out and utilize in analysis the fact, that when a vanadate in concentrated solution is treated with a saturated solution of ammonium chloride, white insolu- ble ammonium metavanadate is deposited.* The method of treatment was modified by v. Hauert in that solid ammonium chloride was added to the solution of the vanadate, as concen- trated as possible, until it failed to dissolve, the mixture allowed to stand and then treated with a large amount of strong alco- hol, the precipitate filtered off, washed with alcohol, dried, ignited in a covered platinum crucible until all ammonium chloride was volatilized, and the residue ignited carefully with ammonium nitrate. Roscoet was unable to obtain exact qnan- titative results by this method on account of the solubility of the ammonium metavanadate in the alcoholic mixture and the danger of mechanical loss during the ignition. Holverscheit also, in testing v. Hauer’s method,§ noted loss of vanadium, due to solubility of the ammonium vanadate in the alcoholic liquid, finding in every case vanadium in the filtrate by means of ammonium sulphide or by hydrogen dioxide. In the average -of six determinations Holverscheit found a loss of 0°0015 grm. ealeulated as V,O,. Another modification of the method was proposed by Ditte,| who, finding that precipitation by an excess of ammonium chloride was complete in a solution made color- less by boiling with free ammonia, attributed the deficiency in the amount of V,O, found after precipitation under the pre- scribed conditions, to volatilization of the vanadium during igni- tion under the influence of ammonium chloride, and endeavored to avoid liability to such error by making it certain that no ammonium chloride should remain with the metavanadate at the time of ignition. To this end, the solution made colorless by boiling with ammonia was cooled to 30°-40°, nearly satu- rated with ammonium chloride and finally treated with four or five times its volume of alcohol; the precipitate thus thrown down was filtered off, washed with absolute alcohol until free from ammonium chloride, dried and ignited, the carbonized residue having been washed with nitric acid before the final ignition. Holverscheit’s criticism of Ditte’s process consisted in showing that losses which may occur in the ignition, and * Ann. Phys. xeviii, 54, 1831. + Jour. Prakt. Chem., lxix, 388. ¢ Ann. Chem. Suppl., Vili, 101, $ Inaug. Diss., Berlin, 1890, p. 11, et seq. | Ee pe- Rend., civ, 982. . 206 Gooch and Gilbert—Ammonium Vanadate. which were found to be trifling when care was used, are mechanical and not due to volatilization ; and, secondly, that in his experience the average error of seven trials resulted in a loss of 0:0029 grm. whether upon 0:1398 grm. or 0:2796 grm. of V,O,. Holverscheit rejects both the method of v. Hauer and that of Ditte as inexact on account of the solubility of the ammonium metavanadate. In 1883,* previous to the proposal of Ditte, Wolcott Gibbs applied in the determination of vanadic acid in the vanadio- molybdates (and sometimes in vanadio tungstates), another and much simpler modification of the method of Berzelius. Gibbs’ method consists in boiling the double vanadate with ammonia _ (to convert the complex salt into a mixture of vanadate and — molybdate), adding a saturated solution of ammonium chloride in large excess, concentrating the liquid kept alkaline with ammonia to a small volume, standing twenty-four hours, col- lecting the precipitated ammonium vanadate upon an asbestos filter in a perforated crucible, washing with a cold saturated solution of ammonium chloride, and, either igniting the pre- cipitate and weighing the residue of V,O, upon the asbestos, or dissolving the precipitate with boiling water, reducing to the condition of V,O, and titrating by permanganate. This method is called in question by Rosenheim,t who gives analyt- ical results of certain experiments which, according to Rosen- heim’s description, are not at all upon the lines laid down by Gibbs. In the first place nothing is said by Rosenheim as to concentrating the mixture toa relatively small volume after adding a saturated solution of ammonium chloride in very large excess; and in the second place Gibbs did not make the final washing with dilute alcohol, as Rosenheim says he did, but finished the washing with a cold saturated solution of pure ammonium chloride. Rosenheim’s variation of the experi- mental procedure in these important particulars, vitiates his conclusions with regard to the precipitation of vanadie acid from solution by ammonium chloride, that “small amounts nevertheless remain, as Roscoe rightly affirms, in solution.” Rosenheim’s opinions of the method are echoed by Milch,t Liebert§ and Euler.| We have thought it desirable, therefore, to investigate anew the question as to whether the precipitation of ammonium metavanadate by ammonium chloride is complete enough to place that mode of separating vanadic acid from solutions of its salts within the list of good analytical methods. The ammonium vanadate used in our experiments was ana- * Proc. Am. Acad., x, 242, 249; Am. Chem. Jour., v, 371, 378. + Inaug. Diss., Berlin, 1888. t Inaug. Diss., Berlin, 1887. § Inaug. Diss., Halle, 1891. || Inaug. Diss., Berlin, 1895. Coos —— Gooch and Gilbert—Ammonium Vanadate. 207 lyzed by the iodometric method of Holverscheit,* and found to contain 76°14 per cent of V,O,. The ammonium chloride employed was shown to be pure and free from iron by heating a solution of it to boiling, adding bromine water and a slight excess of ammonia, and filtering. No residue whatever remained upon the filter. In each experiment a weighed portion of ammonium vana- date was put in a small beaker and heated with about 25° of water and a few drops of ammonia upon the steam bath until solution was complete. To the solution were added 25° of a cold saturated solution of anmonium chloride and a few drops of ammonia. The mixture remained upon the steam bath, with addition from time to time of a little ammonia to keep the metavanadate of normal composition and colorless, until the volume had been reduced to about 25°, and was then cooled. On cooling, a small amount of ammonium chloride crystallized out, but only a little if the proportion had been properly adjusted. If too large an amount of ammonium chloride erystallized out, it was nearly redissolved by the cautious addi- tion of ammonium hydroxide. The mixture was allowed to stand twenty-four hours to insure complete crystallization of the ammonium metavanadate, and was then filtered on a weighed asbestos filter and perforated crucible, the precipitate being transferred and washed with a cold saturated solution of ammonium chloride. Crucible and precipitate were heated, at first very gently to drive off the ammonium chloride without occasioning mechanical loss of the vanadium, and finally to redness and fusion of the pentoxide remaining. At the outset some difficulty was occasionally found in removing from the walls of the beaker the adherent crystals of ammonium vana- date, but this difficulty was overcome, in the experiments recorded, by the device of forming upon the walls of the beaker before using it a film of paraffin of extreme thinness by rinsing the beaker with a dilute solution of paraffin in naphtha (0°5 gram. of paraffin in 300° of naphtha) and allowing the naphtha to evaporate. Crystals of the vanadate adhering to the walls of the beaker thus previously prepared, are easily removed by means of the ordinary rubber or “ policeman.” Table I contains the record of six consecutive experiments made after some preliminary study of the method. The washings and filtrate were in several instances acidified with hydrochloric acid and tested with hydrogen dioxide without giving indication of the presence of vanadium. These results are sufficient to show that the method of Gibbs is capable of yielding an analytical separation of value, but as Gibbs pointed out it is ordinarily preferable to estimate the * Inaug. Diss., Berlin, 1890, p. 49. 208 Gooch and Gilbert—Ammonium Vanadate. renee h f “TaBLe I. eta NH; VO; taken. V.O; present. V.O; found. Error. grams. grams. grams. grams. 0°5 0°3807 0°3814 0:0007 + 0°5 if 0°3818 — 0°0011+ 0°5 ip C°3813 0°0006 + Oro. es 0°3808 0°0001 + 0°5 os 0°3808 0°0001 + 0°5 = 0°3799 ~ 0°0008— | vanadium by volumetric means rather than to go through the tedious and exacting process of ignition to recover the vana- dium pentoxide. Gibbs used the method of reduction by hydrogen sulphide, and titration of the tetroxide by perman- ganate, but for the purpose of testing the method we have thought it best to use the same method for determining the metavanadate separated which was used to determine the com- position of the vanadate taken, viz., Holverscheit’s iodometric method. In the beginning some trouble was experienced in the proper handling of the separated vanadate for this purpose. To dissolve the precipitate in hot water introduced too much hot water into the distilling flask; filtering on paper and then putting paper and vanadate into the flask together introduced an error, due probably to the action of the freed bromine upon the paper. The difficulty was tinally overcome satisfactorily by collecting and washing the separated ammonium metavana- date upon asbestos felt deposited upon a perforated platinum cone of considerable size,*.rolling up the felt enclosing the crystals of vanadate, then putting asbestos and vanadium into the distillation flask, without addition of any water, ready for the addition of potassium bromide and hydrochloric acid according to Holverscheit. The use of so much asbestos made it difficult, however, to boil the mixture of acid, bromide, vana- dium and asbestos, so recourse was taken to heating this mix- ture in the hot air chamber of a high temperature parafiin bath. The mass of asbestos made it necessary to use more hydro- chloric acid to overcome the viscosity of the mixture, and the use of so much acid introduced the element of danger that the volatilization of the acid to the receiver containing potassium iodide might, in presence of air, set free iodine outside the reaction of the process; so the flask was connected with a car- bon dioxide generator, and the operation was carried on in an atmosphere of carbon dioxide. With the exception of the paraffin bath substituted for the burner as a source of heat, the arrangement of the apparatus is shown in the accompanying figure. Following with 1:5 grams of potassium bromide, the introduction of asbestos and vanadate, the distillation flask B * Am. Chem. Jour., vol. i, p. 320. _ Gooch and Gilbert—Ammonium Vanadate. 209 was connected, as shown in the figure, with the receiver charged with a solution of 2°5 grms. of potassium iodide in boiled water, and the apparatus was filled with carbon dioxide. The stop- cock of A was closed, the bulb of A was charged with 50™ of strong hydrochloric acid, the connection with the carbon diox- ide generator was again made, with care to displace all residual air from the bulb. The acid was introduced into B by opening the stopcock and, in a gentle current of carbon dioxide, the heating was continued an hour after the development of color in the receiver showed that bromine was coming over from the flask. The iodine set free in the receiver was titrated with sodium thiosulphate standardized against iodine of value known by comparison with a arsenious acid. ‘The standard of the ammonium vanadate taken, as determined by the Holverscheit method in its simple form, was found to be unchanged when portions of the salt were treated according to the modification necessitated by the presence of so much asbestos in the trial tests, viz., In presence of more acid and in an atmosphere of carbon dioxide. In this manner the determinations of the following table were made: TaBLeE II. Standard NH,VOs; taken. Na.S.0; used. V.O; found. Error. grams. em? grams. grams. 0°1000 8°35 0°0760 0:0001— 0°1000 8°39 0:0764 0°0003 + 0°1000 8°38 0:0763 0°0002 + 0°1000 8°37 0°'0962 0:0001 + 0°1000 8°32 0°0757 0°0004— 0°1000 8°25 0:0751 0:0010— 0°1000 8°36 00761 0°0000 ‘0°1000 8°33 0°0758 0°0003— 210 ~ Gooch and Gilbert—Ammonium Vanadate. - These results, representing determinations of the vanadium pentoxide in the ammonium metavanadate after separation by the same method used in determining the amount of pentoxide in the vanadate taken, abundantly confirm the conclusions reached by a consideration of the results of Table I. So it appears that the criticism of Rosenheim, obviously made undera misapprehension of the details of the Gibbs method, to which Milch, Liebert and Euler give their acqui- escence, is unfounded. The process of Gibbs gives a practically complete precipitation of ammonium vanadate, when to the solution of the soluble vanadate such an excess of ammonium chloride, with a little ammonia, is added, that the solution, after concentration and cooling, deposits ammonium chloride, and the mixture is allowed to stand twenty-four hours. Should too much ammonium chloride for convenient handling erystal- lize out on cooling, this is to be redissolved by the careful addition of ammonia; but care should be taken that after standing, a little solid ammonium chloride and free ammonia should still remain in the mixture. The precipitated ammo- - nium vanadate is to be washed with a cold saturated solution of pure ammonium chloride, and the vanadium in the vanadate determined by any appropriate means. Volumetric processes are to be preferred to the slow ignition. We do not recom- mend as a suitable procedure for ordinary use the complicated modification of the Holverscheit method, which was employed in this investigation in order that the same method of determi- nation of vanadium might be used before and after the separa- tion process. Reduction as suggested by Gibbs, and titration by permanganate or the iodimetric estimation of Browning,* should be of service in ordinary cases. * Zeitschr. Anorg. Chem., vii, 158. 4 “ “ 9 Hillebrand and Penjfield—TLhe Alunite-Jarosite Group. 211 Art. XX V.—Some Additions to the Alunite-Jarosite Group of Minerals ; by W. F. HILLEBRAND and 8. L. PENFIELD. CONCERNING two new varieties of jarosite which will be described in the present communication, one is from Nevada, and was collected by Mr. H. W. Turner of the United States Geological Survey and sent to the survey laboratory at Wash- ington for identification; the other is from New Mexico, and was sent by Mr. J. H. Porter of Denver, Colorado, to the Mineralogical Laboratory of the Sheffield Scientific School. Except for slight differences in color the two minerals look exactly alike, each consisting of minute, isolated, tabular crys- tals, which, as may be seen with the microscope, consist of com- binations of a rhombohedron with largely developed basal planes. By chance it happened that the present writers dis- covered that they were both engaged in the investigation of compounds belonging evidently to the same group, and it was _ decided to bring the results together into one paper. Natrojarosite. The material collected by Mr. Turner was obtained on the east side of Soda Springs Valley, Nevada, on the road from Sodaville to the Vulcan Copper i Mine. It consists of a glistening powder, made up of perfect crystals having the habit shown in figure 1, although generally only one rhom- . bohedron, 7, is present instead of two, as shown in the figure. The largest crystals observed were 0°15™™ wide and 0:025™™ thick, and. the general average would not be over half that size. In spite of being so minute, however, it was possible to measure the angles of the crystals with the reflection goniometer, the chief difficulty arising not so much from their small size as from the vicinal character of the basal planes. After repeated trials a crystal was - found having a fairly good basal plane, and from this crystal the following angles were obtained : Caleu- Measured. Measured. lated. Car, 0001, 1011=51° 53 cAs, 0001 ,0221=68° 42’ 68° 35’ CAT , 0001 A. 1101=51- 53 CNS GCOOKA 202 = 68) 4852 - Sees eanr, OOOLA O111=52 26 fete wot A VIO S86 55.8554 Am, Jour. Sc1.—FourtTH SERIES, VoL. XIV, No. 81.—SEPTEMBER, 1902. 15 212 Hillebrand and Penfield—Additions to the The crystals belong to the rhombohedral division of the hexagonal system, and the angle cA7, 51° 53’, which is prob- ably very nearly correct, has been assumed as fundamental, and from it the following axial ratio has been calculated : C= 1°104. That the axial ratio as given is very near the truth is shown by the fact that the measurements of cas and rar do not vary many minutes from the calculated values; while on a number of other crystals, measurement of the angle cay, though varying considerably, was found to be not far from 52°. The angles of car and 7A?’ of the ordinary potassium jarosite are 55° 16’ and 90° 45’, respectively. Under the microscope the crystals exhibit normal optical properties. Using a high power lens and convergent light, the thicker crystals show the dark cross and the beginnings of the first ring of the interference figure. The birefringence is negative. ‘The color of single crystals, when seen under the microscope in transmitted light, is golden-yellow. Many of the crystals show numerous brown inelusions. The color shown by a mass of the erystals is yellowish-brown, and the material glistens, owing to reflections from the basal planes of the minute crystals. The material used for the chemical analysis was the purest that could be obtained, although crystals containing the brown- ish inclusions just aS, Peould not be avoided, and there were occasional brown ferruginous particles mixed with the crystals. The specific gravity of the material was found to be 3°18 at 380°5° C. The results of the analysis by Hillebrand are as follows: Ratio. Ke.0.. 5. 2a are 0-319 3-29 Na. Of 7. poet eee ae a BOS ea 0°35 0-004 SO, Oe ae a eee 0°387 4°00 ER O below W0S os 43e"2 Ore HH. O above 108° 2: : 11°03 0°613 6°33 igs eee: pools see BRO OAs ee 0°23 Oe rr re ye 0:04 99°94 The ratio of Fe,O,: Na,O:SO,:H,0O is evidently 3:1:4:6 as in ordinary jarosite, where the alkali is potash instead of *Of the soda °22 per cent is not extracted by hot water after full ignition of the mineral and hence may belong to a feldspar or some other foreign mineral. Only 5°81 per cent is assumed to belong to the jarosite and used in deriving the molecular value. apts Liha. até, ote ee f LL ee __ * «i “. a 4 4 5 r Alunite-Jarosite Group of Minerals. 218 soda. The slight excess of Fe,O, and H,O, as indicated by the ratio, is evidently due to some ferric hydroxide; probably the dark ferruginous impurities seen under the microscope are in part responsible for this, and there are also traces of some arsenate and silicate present. Regarding the excess of Fe,O, and H,O as due to impurities, it is found that 94 per cent of the material analyzed may be regarded as pure natrojarosite, as indicated below : After deducting Theory for impurities. NaeFe.[/OH]i2[SOz].. eh ) eee 46°43 or 49°39 49°49 AO er. Sah PO ss BOGE S 6°39 Te Ore ite od OS ae ot OSG eee 2 a 30°96 “ 32°94 32°99 Oe NOra br Sk bE TD 11°13 94°00 100°00 100'00 That six per cent of impurities should be present in a crys- talline powder such as analyzed is not surprising, when it is taken into consideration that it would require something like 2,500,000 erystals to make one gram of material, the estima- tion being based on the assumption that the crystals are 0°-10™™ in axial diameter and 0:02" thick, which is certainly above their average size. Among the specimens from Cook’s Peak, New Mexico, sent to the Sheffield Laboratory by Mr. Porter, were sorne masses of a rather firmly cemented aggregate of minute crystals of a mineral of the jarosite group. The specimens are of a brown- ish-yellow color, and have in places the glistening appearance of a mica-schist. They also look as though they had been sub- jected to pressure and had been somewhat sheared. The material is rather easily crushed, and the powder when exam- ined with the microscope exhibits the properties of the natro- jarosite just described. The crystals are associated with a little limonite and quartz, and pure material for analysis could not be obtained. Only a partial analysis, therefore, was under- taken with the following results : Tick Os Soe ce 55°60 INGOM Se rea LS 4°49 109 (se a SR ee 0°77 AIO) ps SL 8 0°96 SO, and H,O were present but not determined. The results are sufficient to indicate that the material is essentially natro- jarosite. Plumbojarosite. _ This material is from Cook’s Peak; New Mexico. It occurs as a glistening, crystalline powder and as loosely cohering 214 Hillebrand and Penjfield—Additions to the masses which may easily be crushed by pressure between the fingers. The crystals are very symmetrical, and are exactly like those of natrojarosite, figure 1, although generally only one rhombohedron » is present. On the average the crystals are a trifle smaller and noticeably thinner than those of natro- jarosite. A number of crystals were measured on the reflect- Ing goniometer, the chief difficulty arising rather from the vicinal character of the faces than from their small size. One unusually large crystal, 0°28" broad and 0:015™™ thick, was finally found, having the development shown in figure 2, which is unusual, for generally 7 (1011) and not s (0221) is the prevailing rhom- bohedron. Fortunately the crystal koe > was so taken up on a minute point Qs os of wax that the measurement of sas in three rhombohedral zones was possible. The results of five measurements of sas over the upper and lower pole edges varied between 109° 5’ and 109° 30’, the average being 109° 16’; while six measurements over the middle edges varied between 70° 10’ and 71° 00’, the average being 70° 36’. The average of the two supplemen- tary values gives sas, 22010221 = 109° 20’, which has been assumed as fundamental, and from it the following axial ratio has been calculated : 9 ~ C= W216: On the crystal from which the foregoing measurements were obtained the basal plane was vicinal and hence no reliable measurements of cas could be had from it. On a number of other crystals, however, the angle of cx~7 was measured with varying results, the variation resulting from the uncertainty of the reflections from the basal planes. Four measurements of car, which were recorded in the note-book as derived from the best reflections, varied between 54° 15’ and 54° 44’, the average being 54° 30’, while cn7, 0001, 1011, by calculation from the fundamental measurement, is 54° 82’. Hence it may be assumed that the axial ratio as established is reasonably exact. The calculated value of rA7, 1011, 1101, is 89° 42". In polarized light the crystals exhibit normal optical prop- erties and negative birefringence. Being on the average thin- ner than crystals of natrojarosite, it is seldom that, with the highest powers and convergent light, even the beginning of the first ring of the uniaxial interference figure is visible. Individual crystals show under the microscope in transmitted light a golden-yellow color. A mass of crystals has the appear- ance of a glistening dark-brown powder, the color being decidedly darker than that of natrojarosite. Alunite-Jarosite Group of Minerals. 215 The analysis of the mineral was made on the very best material, having a specific gravity of 3°665 at 30°C. The results are surprising, and were wholly unlooked for, since it is found that this jarosite contains lead in the place of alkalies. The results by Hillebrand are as follows: 15> He Wi. IV. = Mean. _—_—Ratio. Mewes |. 49°36 42°38 42°37 0°265 ) ... Paes (fo) soeOeeey 2b 10 0:001 : a 19°69 19:99 19°89 19°79 19°84 0°089 1-05 a ory 17 139 “21+ =r _ =a 27-65 2e-07 27°06 0°338 4-00 H,O below 105° = 02 : 02 H,O above 105° 9°59 — 9:49 9°54 0530 6:27 2 a 56 51 “47 51 CL eee "27 “27 “21 2 "05 05 UL ‘Ol ‘O1 100715 The ratio of Fe,O,: PbO: SO,: HO is very close to 3:1:4:6, indicating that the mineral is a variety of jarosite, and the slight excess of Fe,O,, H,O, and PbO+ alkalies, may be accounted for by assuming that slight impurities are present, partly ferric hydroxide, in part some lead salt, and perhaps a soluble silicate, as shown by the complete solubility of the silica in _acids. Assuming that the ratio is exactly 3:1:4:6, it is found that 4°36 per cent of impurities are present, and the remaining 95°64 per cent may then be regarded as plumbojarosite, as follows : Theory for PbFe.[OH]:2[SO.].. ety 83 420°s9 © or) 42°44 12) 3 cae aie 18°86 = 19°72 Se et 2706 = = 28-29 ERO. gpg - |) 9°55 95°64 100°00 Since it took probably 2,500,000 crystals of natrojarosite to make one gram of material, it certainly must have taken fully 4,000,000 to make a gram of plumbojarosite, for the crystals of the latter mineral, though somewhat heavier, are decidedly thinner than those of the former; hence the presence of 4°5 *The presence of alumina was not definitely proved. The figures here given are the differences between the several weights of the ammonia pre- cipitates and those of the ferric iron in them, as determined by permanganate after reduction by hydrogen sulphide. + Probably somewhat high. 216 Hillebrand and Penfield—Additions to the. per cent of impurities in such a crystalline product is not to be wondered at. Jarosite and Alunite. As seen from the analyses of these minerals which have been published, the alkali metal they contain is almost always potas- slum, though sodium is at times present. -The formulas assigned to the two minerals are therefore K ,0 +3Fe,0,+480, +6H, O and K,0+3AI],O, + 48O, + 6H,O, ‘which may be variously expressed, as will be indicated later. A mineral corresponding to natrojarosite of this article, though containing a little potash, has been described by W. P. Headden* from the Buxton mine, Lawrence Co., 8. D. The crystals are described as scales, consisting of a combination of base and rhombohedron. The material analyzed was evidently somewhat impure, as quartz and some As,O, are reported. As the As,O, evidently does not belong to jarosite, the assump- tion may be made that some scorodite, FeAsO,-2H,0, is present, and the results of Headden’s analysis: may then be interpreted as follows: Original Scorodite Natro- analysis. and quartz. jarosite. Ratio. | Wel @ PRMGpd Saree sag 46°27 1°60 44:67 or 50°10 3°13 bcs 6 Slane y 4°35 4°35. 35 4°86 LGA epee) 1°47 1°47 ed 1°65 1:04 EE sa Sha gee RA 0°39 USo ae 0-44 Se gt ENN Ce ai 28°46 28°46 .: 31°98 4°00 Eira! teas! 10°55 0°72 9°83 * 11:02 6°13 62 4358 AM SRD, 2°36 2°36 bee ae Guariaties hss th 6°10 6°10 feat eee 99°95 10°78 89°17 100°00 Thus, assuming the presence of 4°68 per cent of scorodite and 6°10 of quartz, and deducting them, the remainder agrees very closely with natrojarosite, giving a good ratio, very near pede ass. Alunite ‘containing considerable soda has been described by W. Crosst from Rosita Hills, Colorado, and by E. B. Hurl- burtt from Red Mountain, Colorado, and analyses of both minerals show about equal percentages of K,O and Na,QO, or a molecular ratio of K,0:Na,O = 4:7. The occurrence, there- fore, of sodium in the jarosite- -alunite group is in accordance with previous observations, but the case is quite different with lead. As far as the present writers are aware, this is the first instance on record where lead has been observed isomorphous with the alkali metals. It is interesting to note that the alunite from Red Mountain, Colorado, occurs as a crystalline powder, * This Journal (8), a p. 24, 1893. + Ibid. (8), xli, p. 472, 1891. t Ibid. (8), xlviii, p. 180, 1894. —— ee Se Alunite-Jarosite Group of Minerals. 217 the crystals being exactly like those of natrojarosite and plum- bojarosite, except that they are «a trifle smaller and white, or colorless when seen under the microscope. From a chemical standpoint the most interesting feature of the new minerals is the light they throw upon the iso- morphism of potassium, sodium and lead. Ordinarily, even potassium and sodium are not isomorphous, as shown by the fact that their simple salts seldom crystallize in the same form. Although KCl and NaCl both erystallize in cubes, it is not certain that both salts belong to the same group of the iso- metric system. It has been shown, for example, by etching, that KCl crystallizes like NH,Cl in the plagihedral group of the isometric system, while the etchings produced on halite | seem to indicate that it crystallizes in the normal group. Again at Stassfurt, Germany, sylvite and halite both occur erystallized side by side upon the same hand specimen, instead of mixing as isomorphous molecules. Even in such complex molecular compounds as the feldspars, the potassium and sodium salts crystallize as orthoclase and albite, rather than as - isomorphous mixtures. Lastly potassium has a strong tend- ency to form alums which is not shared by sodium. In con- trast to these differences in chemical nature, we have in the jarosite-alunite group of minerals not only the alkali-metals, potassium and sodium, but, what seems still more remarkable, lead, playing the same role in the compounds, and yielding erystals which are surprisingly alike in all their physical prop- erties. The writers can at present offer no other reason for the isomorphism in the group of minerals under consideration than that the alkalies and lead play so small a role, and the remaining constituents so prominent a part in the complex chemical molecules, that the latter control or dominate the erystallization by virtue of what may be called their mass effect. The alunite from Red Mountain, described by Hurlburt, was analyzed in the Sheffield Mineralogical Laboratory under the direction of one of the present writers, and it was found that water was first expelled from the compound at a rather high temperature, thus indicating that the mineral contains hydroxyl and no water of crystallization: accordingly it was shown that the seemingly complex formula of the mineral, expressed by the ratio Al,O,: K,0:SO,: H,O = 8:1:4: 6, may be much simplified to K[ Ai(OH),],[SO,],.. In the light of the present investigation it now seems best to abandon the above simple formula and adopt one containing double the number of atoms, in order to make clear the isomorphism between K,, Na, and Pb. The formulas of the minerals of the group would then be expressed as follows : 218 LMillebrand and Penfield—Additions to the Alunite, K, |; Al(OH);|,[80,],° or “K,AlfOH] son: Natroalunite, Na,[Al(OH),|,[SO,], or Na,Al JOH] [SO, J arosite, K,| Fe(OH).),(S0,], or KFe lO sem) Natrojarosite, . Na,[Fe(OH))|[S0,],: or Nae) OR eisams Plumbojarosite, Pbj|Fe(OH),|,,[SO,|, or PbFe,OH],,[/S50 In the case of the lead compound one atom of lead, and in the others two atoms of either potassium or sodium, are com- bined in complex molecules containing fifty other atoms; hence that the complex of fifty atoms, to the right of the K,, Na, and Pb in the foregoing formulas, should control or domi- nate crystallization by virtue of mass effect, and condition an isomorphism between such unlike elements as sodium, potas- sium and lead, is not so surprising as would at first appear. Having adopted the double formulas, as given above, there are numerous ways of writing developed formulas, of which the following are perhaps the simplest and most satisfactory : 4 ) — 414 OS =O HO WAN OR Ho>Fe—O O ae Oar HO a 3 _OH Ho>Fe—9 So. b= Oe Ss — O—Fe< og HO OH Ho>Fe—O . y 0 Oi FeO 8-0 er, eG HO Bt ( 6)! 2 Ho>Fe—-ON At \ 4ZO0O—-K eon a Ou IOs LOS Sf aa a es aR EWE 0 _-OH OH It is interesting to note that although K,, Na, and Pb play so small a rdle in the alunite-jarosite molecules, the substitution of Na, for K, is attended by quite a marked variation in the. angles of the crystals, greater in fact than is generally observed in isomorphous replacements. That alunite and jarosite con- taining potash would be nearly alike in their angles is expected, since crystals of corundum and hematite are surprisingly alike as shown by the following comparison : NEY Foe Oe Axial length. PAT CAT CorundumyAlO. oc.” 13630 93° 56’ 57° 34! Hematite, Fe,O,-.--- 1°3656 94 00 57 37 Ad £ Alunite-Jarosite Group of Minerals. 219 The relations of the minerals of the alunite-jarosite group are as follows: Axial length. ae Gar Birefringence. Ai 1°252 90° 50’ . 55° 192’ positive Jarosite _.------ 1°245 90 45 55. 16 negative Natrojarosite _.. 1°104 85 54 51 58 negative Plumbojarosite_- 1°216 89 42 54 32 negative From the foregoing table it is seen that the substitution of sodium for potassium in jarosite has brought about greater variation in the angles of the crystals than the substitution of the bivalent metal lead for potassium. The three minerals, natrojarosite, plumbojarosite and the Na-K-alunite from Red Mountain, are very interesting when studied together as microscopic mounts, the crystals being practically alike in size and development, aud illustrating very beautifully on the one hand the isomorphism of aluminum and iron, on the other the isomorphism of potassium, sodium and lead. The three substances must have formed under like conditions, and it is believed that they are solfataric products, formed under the combined action of heat and pressure. Being difficultly soluble, they have formed, like many precip- itates, as fine erystalline powders. The three products just mentioned, when heated in closed tubes behave alike; they suffer no change on gentle heating, but when the temperature is sufficiently high to decompose the chemical molecules, the crystals break up into fine powder or dust, which is carried along by the escaping vapors and deposited for a considerable distance along the sides of the tubes. In addition to water, SO, and SO, are copiously given off during decomposition. In the case of natrojarosite, and the same would doubtless hold true for the Na-K-alunite, it is found that after ignition, one-fourth of the sulphate radical has been retained by the alkali metal, and may be extracted by water. In the case of plumbojarosite, however, all of the sul- phate radical is expelled by ignition, doubtless because the ferric-oxide present serves to decompose any lead sulphate which might have a tendency to form. Anglesite, PbSO,, when heated alone in a closed tube suffers no decomposition, but when finely triturated with limonite and beated, acid water is given off. Finely powdered natrojarosite and plumbojaro- site are slowly but completely soluble in boiling hydrochloric acid. Plumbojarosite when fused with sodium carbonate on charcoal yields globules of lead and a coating of lead oxide. It has seemed to the writers best to designate the new com- pounds described in this article as natrojarosite and plumbo- jJarosite, the names signifying their relation to a well known 220 Hillebrand and Penfield—The Alunite-Jarosite Group. species. Other members of this group will doubtless be found, and the name natroalunite might be employed to designate the two varieties of alunite from Colorado men- tioned on page 216, where the proportion of the soda to the potash molecule is 7:4. It is highly probable that a series of alunite-jarosite compounds could be made artificially. It is with pleasure that the writers acknowledge their indebt- edness to Messrs. Turner and Porter for calling attention to the interesting compounds described in this article. Laboratories of the U. S. Geological Survey, Washington, and of the Sheffield Scientific School, Yale University, New Haven, ; Feb., 1902. Kindle— Niagara Limestones of Hamilton County, Ind. 221 Art. XX VI.—The Niagara Limestones of Hamilton County, Indiana; by EDWaRD M. KINDLE. HAMILTON County is located slightly north of the geographi- cal center of Indiana. The drift in this part of the State is so deep that the Paleozoic rocks are rarely exposed at the surface. Only a few outcrops occur in the county. The most extensive exposure is the one at Connor’s mill on White river, five miles above Noblesville. Two small quarries southwest of Fishers- ville afford an equally good opportunity to study the Paleozoic rocks of the county. Several days were spent by the writer in collecting from the beds exposed at these two localities. Connor’s mill.—The outcrop at Connor’s mill consists of a hard, light buff dolomite, which is exposed for two or three hundred yards below the dam. The beds show a dip of 20° to 40° to the southwest. Above the dam one-third of a mile the limestone outcrops again, dipping 30° to the northwest. The See! is a list of fossils collected from beds exposed below the dam :* MERC RIRIISHS 22 ee ead Oe. PeeIsinGh CF, COMCUMM ..-..-----------4--- Ts EMMMIRM OS SMAIRETOE certo ui el se ee MS > 8 MEMUPLOCTINUS Cf. CTASSUS __ =. ..-- -.-- --2-2- Z Somehsocunm multicostatum_.....-- ..-=-~=122 a. Conchidium sp. -------- ean. tS ot ee eee t UNMEELACIREES | ee. et Ie paeeuMcodonta projunda@ .-.- 2... --.---.-.-- e. mepemcne TROMMOIdalIs._:..2--.-.----- 2-42 e EES SCE EES ae PMEREGEIS 862 oe fer ees ee eke MP OITO CUINUTG 22 ee BERS MIGUUTENSIS 22-0" aL | DRE MCCEI SHG! 8 GOO ee r Mmnmnclan Clogs 6 2. ek gt. amen prites Cy. sericea... 2. 22-2 2-2 T.. EET SSS 7B ed a ee ot Platyostoma cf. niagarense .....-.---...---- C. Spherexochus CIN SS Se a a: EennmCnE NIT GOKEHSIS (222 is lk Ll C. EME eer ee le. MOIS Ch IPIGUIOMOUS PS Cc. ETE ET Se ey ee rr Fishersburg quarries.—Southwest of Fishersburg one-half mile a very pure white sandstone has been quarried for glass * The species listed will be described and figured in a future paper. 222 Kindle—Niagara Limestones of Hamilton County, Ind. Figure 2.—Fishersburg quarry, showing unconformity between Niagara limestone and underlying sandstone. Kindle—Niagara Limestones of Hamilton County, Ind. 223 making. It isa fine-grained, massive, loosely-cemented rock, erumbling easily. A buff dolomite, having the same lithologi- cal characteristics as the outcrops at Connor’s mill, rests upon the sandstone.. The line of contact between the two forma- tions is clearly shown in the quarry and is seen to be a very irregular one, resembling unconformity. The sandstone is believed however to be a local lense. Such lenses are known at other localities in the State where both the upper and lower contact with the Niagara limestone is clear. The limestone on either side of the projecting mass of sandstone extends below the surface of the pool which fills the quarry. The limestone beds show a dip of about 35° to the north. A careful search failed to discover any fossils in the sandstone. The fauna of the limestone as well as its physical characters indicate that it belongs to the same formation as the beds at Connor’s mill. A comparatively short time was spent in collecting from the Fishersburg quarries, and for this reascn the following list of fossils from that locality includes fewer species than the pre- ceding list: masemclasme Gf. calicula 222... .222-------- r. EMIS TIES HUGO OTENStS = 225 ssl le e Pep TAO TObUS 8 . olke ns ie Conckwavum multicostatum ....---.-----<---~- a. mnewcemarid Gf. OICOSIGLG ... 2 222 22 -- 2222 225-- Ki Prevamicies sulplanus. ..- 2.13.22. 2.22 2222. - r. EME NOONGO SP... 325 2 es ea tu. C. Men RG ae Pr ue See ae, Gi Mince gerd pisi forms... 2 ee 2-2 ee - rs PL piOena TROMOOTAGIS .......)2---.--. 224. - ¥ Me mmanslis 2) oe A WOH ee IG es el F. MEPeRCMOCNUS TOMIMGEN. ..-. 2-25 .--. 422 5-4 4 F. Beemmeapaie). brisuleadtus 2... 22-2. .2- 122-22) - Fe: MRE Soe Oe RE oe OE Lk YT, Correlation.—Richard Owen described the outcrop at Con- nor’s mill in his report published in 1863,* but offered no opinion as to the age of the beds. The earliest reference to the age of these beds occurs in a report on the geology of Hamilton countyt by Dr. R. T. Brown, who considered them to be of Devonian age. No paleontological evidence was offered in support of this opinion, the author of the report stating that “the outcrops of rock in Hamilton county are * Rep, Ind. Geol. Surv. for 1859-62, p. 102. + 14th Ann. Rep. Ind. Geol. Surv., 1884, p. 27. 224 Kindle—Niagara Limestones of Hamilton County, Ind. quite barren of fossils.’ In 1901* the limestones at Connor’s mill and near Fishersburg were referred by the writer to the Niagara, but the paleontological evidence for this determina- tion was not given. The faunal lists here given clearly show the Niagara age of these beds. The Lockport (Niagara) lime- stone is their probable equivalent in the Niagara group. The Hamilton county outcrops are the most southern expos- ures in the State which show highly tilted Niagara strata. The orogenic disturbances, which caused a general tilting of the Niagara rocks in northern Indiana previous to the begin- ning of Devonian sedimentation, did not affect the southern portion of the State, where they lie nearly horizontal, and are conformable with the Devonian rocks. ‘North of the Ohio river eighty miles the Niagara rocks are slightly unconforma- ble with the Devonian,t+ but nearly horizontal. The Devonian rocks have not been observed in contact with the Niagara in Hamilton county, but it is very probable that they are uncon- formable as they have been shown to be further north in the Wabash valley.t U.S. Geol. Survey, New Haven, Conn., June, 1902. 25th Ann. Rep. Dept. Geol. and Nat. Res., Ind., p. 559. + Kindle 25th Ann. Rept. Dept. Geol. Nat. Hist. enh , plate 16. ¢ Ibid., p. 562. C. Barus— Velocity and Structure of the Nucleus. 225 Art. XXVII.— On the Velocity and the Structure of the Nucleus ; by C. Barus. 1. Nucleation produced by shaking and tts velocity.—Table I contains the results for the absorption velocity, #, of nuclei shaken out of dilute solutions. The data were obtained by measuring the condensational coronas in a spherical vessel (diameter, 2/2 = 30™) in the lapse of time. If the loss of nuclei be regarded as taking place at the walls of the vessel and to constitute a drain on the whole nucleation (7 particles per cub. em.) which moves radially outward at the rate #, then the equation* n= n,e—*"/F may be assumed. The time elapsed, ¢, is usually given in minutes. To deduce from £& the velocity of the nucleus, «, I have for the present regarded it as sufficient to multiply by 6 or preferably by 15/7, so that «=51k. The concentration, c, is given in per cents or grams of dry salt in 100% ™ of solution. It is essential that a definite bulk (usually 500% °™) be used throughout, if the data are to be at once comparable. TaBLeE I.—Nuclei shaken out of solutions by 10 jerks. Bulk of solution usually 500°™?, Nucleation, n = no eg < R= 15", Concen- Nuclea- Absorption Nuclear Solvent. Solute. tration, c. tion,n. velocity, k. velocity, x. % em/min. em/min. Water Water 0° 32 1°5 7°6 85 6°7 34° 26 9°4 48° Water HCl 9) 160 "06 30 "005 140 "02 "10 "00005 80 2°3 E2° Water. H,SO, 6 215 ‘03 15 "003 130 ‘O7 36 Water NaCl. 2 175 ‘01 05 Water CaCl, 2 240 04 20 1 240- a it (double bulk) 1 460 "044 20 Water FeCl, 2 230 us - has, 180 ee ad Water Fe3NO, 12 175 03 "15 "12 160 03 15 Water Al3NO, E2 200 07 "36 "12 80 03 "15 Water Ca2NO, 1-4 260 ‘04 "20 ‘O14 90 ‘02 10 ‘0014 60 "10 “51 * This Journal (4), xiii, pp. 91, 94, 1902. + Note the doubled n and single k. C. Barus— Velocity and Structure of the Nucleus. 226 TABLE I (continued). Concen- Nuclea- Absorption Nuclear Solvent. Solute. tration, ¢. tion,n. velocity,k. velocity, x, Lb cem/min. em/min. Water Ca2NO, 00014 60 1:4 71 Water Alum 5 200 05 “25 (dry) O15 90 i 56 Water Na,SO, 9 450 ‘07 "36 "009 110 “le “61 ‘00009 50 Fad | ne Water H,N NO, 2 190 "03 "15 ‘02 129 “11 56 Water K,SO, 2 280 06 31 "02 -140 07 °36 Water Na,PO, 9 195 06 31 Water Sucrose 2 160 “ts 66 "02 51 19 97 Water Glucose 1°6 150 4 aah ‘016 50 1:0 onl Water Glycerin 26 95 ia 5°6 "026 50 2°3 12° Water Urea 2 110 19 97 Water Alcohol 0 55 4°8 24° 1°6 43 1°8 9° Water Tartaric 2 130 02 10 acid 02 100 02 10 ‘0002 95 “20 bga Benzol Naphtha- 2 90* "04 “20 lene 02 90 ‘03 “5 none 80 "02 "10 Benzol _Paraffine if 130 02 10 O 80 "04 20 _ Benzine none at 2 16 "82 2. Leemarks on the data.—The main deductions from these tables have been briefly given elsewheret and need not there- fore be detailed here. Great caution is necessary because of the inevitable irregularities of the results. The dependence of the nucleation, n, on the concentration ¢, agrees fairly well with the equation, n=n,+A/(log(B/c)), where A and B are constants. Hence in making comparisons, it will be con- venient to refer ail data to the logarithmic concentration, log c, from the peculiar character of the results. In a general way the number of nuclei evolved, caet. par., depends on the mass of solute dissolved per cub. em., and for 1 per cent solu- tions is within rather narrow limits independent of the saline * These data are computed as if the solvent were water. They are thus partly relative. The data needed to find n for benzol are not consistently forthcoming. + Science, xv, pp. 912-914, 1902. C. Barus— Velocity and Structure of the Nucleus. 227 or acid solute taken. For neutral organic solutes, the number, mn, is little more than half as large. This seems then to be in the nature of a class distinction. Pressure decrements of less than 2™ suffice to precipitate the nuclei; but for the small supersaturations, the greater number re-evaporate to the nuclear stage and many exhaustions are needed to throw them out. For the high degrees of supersaturation all nuclei are precipi- tated at once. The number of nuclei generated depends on the bulk of solution shaken and on the intensity of the agita- tion. Hence they seem to arise in the solution itself and not by friction with the walls of the vessel. The attempt to find a limiting number has not yet been successful. Incidental conditions which have not all been traced to their source seem to have considerable influence on n. 3. Persistence of nuclei.—A comparison of the data for n and those of & for the same concentration shows that for the same solution m decreases with log ¢ while # increases with log c, the arena of greatest variation being the very dilute solu- tions which merge into water. Usually the growth of & con- tinues even after the decrease of m has appreciably subsided. Corresponding to the greater m which characterizes the saline solutes as compared with the neutral organic solutes, the veloci- ties of the nuclei of the latter are greater than those of the former, under otherwise like conditions. Nuclei with neutral organic solutes in water are less persistent. Extreme per- sistence may be obtained with the volatile hydrocarbon sol- vents with an appropriate solute, like benzol-paraffine, and often the solute seems to be spontaneously nuclei-producing, © like benzol-naphthalene. In general persistence for a given nucleus is a question of the mass dissolved per cub. em. of the solution ; but cases like water-tartaric acid occur in which a low order of nucleation, m, is associated with exceptional per- sistence, or low values of &. 4. Structure of the nucleus.—From experiments like the present I recently came to the conclusion that all condensation nuclei are concentrated solutions; that the increment of vapor pressure due to increasing convexity is eventually, but slightly before molecular diameters are reached, compensated by a decrement of vapor pressure due either to concentration* or to electric charge.t The latter case is interesting inasmuch as the nuclei are just about large enough that a single electron spread out over the surface would suffice to equilibratet the increment of vapor pressure due to surface tension. The con- centration hypothesis is more straightforward and requires * Science, xv, pp. 912-914, 1902. + This Journai (4), xiii, pp. 400-402, 1902 ; ibid., p. 478. ¢ This Journal (4), xiii, p. 473, 1902. Am. Jour. Scl.—FourtTH Series, Vou. XIV, No. 81.—SEPTEMBER, 1902. 16 228 0. Barus— Velocity and Structure of the Nucleus. less imagination, and it will therefore be chiefly referred to in the following discussion. The nucleus is to be regarded small enough that it is not symmetrically bombarded by the mole- cules of vapor. Hence its velocity is conceived to be inereas- ingly larger as it is smaller, i. e., as the conditions favorable to non-symmetrical bombardment increase. If too large it will be stationary, apart from gravity; if small enough, it must eventually acquire the molecular velocities themselves. 5. The relations of equilibrium here involved are peculiar and need a more detailed elucidation. If vapor pressure increases with increasing convexity, for capillary reasons, but eventually decreases again as a result of the concentration ; i the normal vapor pressure at a flat surface, it follows that as the size of the drop continually decreases the vapor pressure at its surface must pass through a maximum. The accompany- ing diagram” is an attempt to represent the case graphically for two given solutions, by making the vapor pressures the ordi- nates, and the radii of the given droplet of solution the abscissas. The line ad indicates the normal vapor pressures. All particles whose sizes taken from the curve 6m’s’ correspond to the abscissas between s’ and 6 therefore evaporate in the lapse of time, those lying near the maximum, m’, fastest, those lying near s’ or 6 with proportionate slowness, while the latter are also lost by subsidence and may be dismissed from con- sideration. On the other hand, a particle whose radius is. smaller than the abscissa corresponding to s’ will grow so that as’ is the stable radius of the nucleus obtained by shaking the given dilute solution. If the solution is weaker, the droplet shaken out of it will have to evaporate further to reach the critical density of the stable nuclear state, and the increment of vapor pressure due to surface tension will also be larger or the maximum, m, will be higher. The curve bms now represents the conditions and is to be similarly interpreted. * The two curves should have been drawn preferably without intersecting. C. Barus— Velocity and Structure of the Nucleus. 229 If the solvent is pure or contains only a trace of solute, the nucleus will vanish completely, or else the particle left may be too small to serve as a condensation nucleus for a given pres- sure decrement of exhaustion. The size after the lapse of time depends on the fixed quantity of salt originally entrapped. If the vapor is not quite saturated, the chances for evapora- tion will be enhanced. ‘The line a will be correspondingly lowered, but equilibrium may result for a smaller size of nucleus, until eventually the solid saline residue of the nucleus alone is left. In so far as these concentration nuclei occur in the atmosphere, one is justified in concluding that their size (apart from the effects of temperature and barometric pressure on surface tension and vapor density*) will increase under mean atmospheric conditions as they are suspended at higher distances above the earth’s surface, until the levels of perpetual saturation are invaded. 6. There is one outstanding question relating to the time losses which must now be considered. These coefficients, dn/dt, are much smaller for concentrated than for weak solu- tions. This observation was referred to the diffusion of the nucleus and its absorption at the walls of the vessel with dif- ferent velocities, #. The diagram shows, however, that near the points s there must be retarded evaporation for all parti- cles, because of the small differences of vapor pressure remain- ing. Hence the persistence of nuclei shaken out of solutions might be ascribed to this effect. True, no reason is evident why stronger solutions should differ from weak solutions in their rela- tive time losses, d log n/dt. Referring to Table 1 again, solu- tions of CaCl,, H,SO,, which can not dry in a saturated atmos- phere, are seen to show nothing exceptional in their behavior. It may be computed that the stable nucleus is, in this case, not even very concentrated. Special experiments are nevertheless needed to clear up the matter, and they must be so devised as to give direct evidence of the occurrence of diffusion or motion of nuclei, and the value of its amount. If this is large enough to be compatible with the data for & in this chapter, then the hypothesis of retarded evaporation may be dismissed. It is with this end in view that the experiments of the next table are contrived and the results show that the motion of the phosphorus nucleus, as actually observed, is considerably faster than the average case computed for the nuclei in the present chapter, and consequently the interpretation here accepted is corroborated. 7. Motion of nucler directly observed.—Table II shows the velocity of the nuclei as found directly in a tower-like receiver 1 meter high, into the bottom of which the nuclei have been introduced. The height of the fog bank, «’, seen on exhaustion * Note that temperature and elevation produce opposed effects. 230 @. Barus— Velocity and Structure of the Nucleus. after the lapse of a definite number of minutes, give the velocity sought at once, after correcting for the instantaneous elevation of the plane of demarcation due to the withdrawal of non-nucleated air from the top of the apparatus. The table gives the ratios p’/p of pressures after and before exhaustion, respectively. The experiments are very trying, chiefly because of the difficulty of finding the initial position (time ¢ = 0) of the plane of demarcation between clean and nucleated air. For this reason I will also give the height of the fog bank seen on exhaustion after 50 minutes. The table shows that incidental conditions (whether the inflowing filtered air be quite dry or not, ete.), often very subtle, largely influence the results, but a detailed explanation, for which there is no room here, must be given elsewhere. TaBLE II.—Apparent and corrected rates of motion (x! and x) of phosphorus nuclei in different saturated vapors. Height of Pressure- fog bank ratio. Vapor. Apparatus, etc. mx 10°. «x10?. ° after 50™, : em/min. em/min. cm. "83 Benzol Tower 75 61 AQ "78 Toluol Globe 80 62 40 90 ee Tower - 43 39 ei 83 Acetone Tower 58 48 32 4 s Initial rate 75 §2 38 << j{ Amyl Tower, initial ; 100 83 51 e | Alcohol apparent 75 62 46 “ Ethyl Tower 106 88 62 RF Alcohol Dried air 72 60 ee | . Methyl Tower 24 20 29 - Alcohol Dried air 64 53 42 r¢ Water . Estimated* 10,000 8300 — 8. General comparison of nuclear velocities.—It will now be opportune to make a comparison of all the nuclear veloci- ties made in widely different experiments throughout my work. I will begin with the results of my first memoirf on the subject, in which the velocities of phosphorus nuclei in ordinary atmospheric air were studied both by mechanical methods (steam jet and absorption tubes), and by the electrical condenser methods. The mean value of & = 18 em./min. may be taken. Hence in air, « = 90 cm./min., nearly. The num- ber of particles was of the order of x = 10* per cub. em. of air. In more recent experiments and by a methodt of comparing * Rise or fall of the strands or fog filaments. +Experiments with Ionized Air; Smithsonian Contributions, pp. 1-93, 01 t This Journal (4), xiii, p. 92, 1902. C. Barus— Velocity and Structure of the Nucleus. 231 coronas of different orders, for phosphorus and other nuclei, present in saturated water vapor to the average extent of 10° per cub. em., the value &= °1 cm./min. was ascertained. This is equivalent to «=°5 cm./min., in air saturated with water vapor. This datum may now be compared with the diffusion veloci- ties of Table II of this chapter, in which fresh phosphorus and other nuclei were used, densely distributed and tested in a variety of vapors, alcoholic, hydrocarbon, ete. The usual values of diffusion velocity lie between « = ‘5 ecm./min. and ‘9 cm./min., being thus of the order of the preceding case. Water vapor itself did not admit of measurement. The value estimated from the filamentary advance immediately after the nuclei enter, 80 cm./min., agrees more closely with the case for atmospheric air at the beginning of the paragraph. -As stated elsewhere, there is much in the behavior of water which is left unexplained. When the nuclei are first introduced into the mixture of air and saturated water vapor, the air effect does not seem to be negligible. Finally the experiments on the evanescence of the nuclei produced by shaking solutions lead to a series of values of & as follows. A few hundred nuclei per cub. cm. were usually present after shaking the solutions, and less than 50 (usually) after shaking pure water. For the saline solutions of 1-3 per cent, of -01 per cent and of -0001 per cent, respectively, « = °25, ‘40, and 10. For pure - water « = 25 or even 50. For aqueous solutions of solid neutral organic solutes of 1-3 per cent, and ‘01 per cent, « =°8, and 3, respectively. The acid organic solutes like tartaric acid seem to behave quite differently. The solutions of this body of 2 per cent, -02 per cent and -0002 per cent, showed diffusion velocities of « = ‘1, ‘1, and 1-0, respectively, thus evidencing uniformly greater persistence of nucleation than even the saline bodies. For neutral liquid organic solutes in aqueous solution of 1-3 per cent and -Ol per cent e=6and 12. Nuclei from these bodies are thus very fleeting. Finally for hydrocarbon solution of solid hydrocarbons of 1-3 per cent, « = ‘10 or ‘20, not differing much in persistence, etc., from the salt solutions. The total range found for the diffusion velocity of nuclei produced by shaking solutions of less than 3 per cent is thus from « = ‘1 to 50 cm./min., increasing with the degree of dilution-of the solution, the largest value cited (pure water) closely approaching the datum for phosphorus nuclei in atmos- pheric air, « = 90 cm./min. These variations of the velocity of the nuclei produced by 232 =. Barus— Velocity and Structure of the Nucleus. shaking and its relation to the order of values found in the direct experiments with phosphorus nuclei given in Table II, is accounted for by the thermodynamic hypothesis for their occurrence, which makes them particles of concentrated solu- tion. The size of the nucleus for a given solvent depends essentially on the extremely small mass of solute which it hap- pens to contain. It is larger when shaken from the more concentrated dilute solutions than from the weaker solutions, because the critical density is reached in the former case with less evaporation and the capillary increment of vapor pressure to be compensated is at the same time smaller. Thus it is quite reasonable to suppose that the nucleus obtained from phosphorus or other emanations will be smaller and therefore more mobile than the nucleus shaken out of the more concentrated dilute solutions, but not so small in general as the nuclei shaken out of pure water or any other pure sol- vent, in which the amount of solute is an actually vanishing quantity. To carry out this comparison one should eliminate the peculiar features of water and use the same neutral solvent in both cases: but if the above results for benzol in Tables I and II are brought together, the same inferences follow. 9. Conclusion.— Among the tenable hypotheses, each of which has some peculiarity in its favor, the above paragraphs are believed to sustain the inference that condensation nuclei in a nearly saturated medium are concentrated solutions. In proportion as the medium is less saturated, they may pass into the dry solute if such a one is present. The conditions of equilibrium which are supposed to intervene are given in § 5. Evidences in favor of this point of view are varied. In the first place the velocity and therefore the size of the nucleus, no matter of what origin, varies with the medium in which it is suspended or is generated. Two mechanical suggestions may be offered in explanation: either the nucleus condenses more or less vapor spontaneously as assumed above, or the nuclei themselves cohere into greater or smaller clusters, depending on the medium. I pointed out that the latter case calls to mind the suspension of clays, ete., in water or other liquids. The endeavor to refer the differences to specific inductive capacity or to the ionizing properties of the liquids breaks. down with such solvents as acetone. Of all the nuclei tested, those produced by shaking seemed to be simplest as to their origin and therefore best adapted to throw light on the subject. At first sight such a nucleus should be the dry residue left after evaporation ; but the effi- ciency of gaseous solutes like HCl, etc., shows that a solid solute is not necessary. In view of the astonishingly small quantity of solute which suftices to produce persistence, how- C. Barus— Velocity and Structure of the Nucleus. 238 ever, it is a question whether the total absence of solid solute in experiments with acid solutions can be guaranteed. The next evidence is perhaps better; if it were a mere question of fixed residue, then the neutral organic solutes like the sugars, urea, glycerine, etc., should be quite as effective in producing persistent nuclei as the saline solutes. Table I shows that this is not the case. Finally since the pressure decrement of much less than 2° of mercury prodnees precipitation, the vapor pres- sure excess at the surface of the nucleus is small, and quite within the limits of reduction produced by solution. The evidence from hygroscopic bodies in which dry residues are out of the question, has already been given. § 6. Turning now to the electrical point of view, one notices at the otitset a marked similarity in the trend of the above results to the researches of Lenard* on the electricity produced by waterfalls and jets. He showed that pure water when prop- erly comminuted by spraying was made electrically positive while the surrounding air became electrically negative, that these charges originated in the liquid in contact with air and could be indefinitely increased with the intensity with which the spray was projected against a solid obstacle. This is in harmony with the conditions for producing the above nuclei. Again, the electric manifestations stated for pure water were totally changed in character by the addition of mere traces of solute to the water. Thus in case of dilute salt solutions the liquid on comminution became negatively charged, and the air_ positively charged. As little as 005 per cent of salt was sufficient to nearly wipe out the water effect. This then is quite similar to the conditions of persistence of nuclei instanced in the above tables. | Lenard’s explanation is in terms of the ‘ Doppelschicht,” which for pure water is conceived to be negative outward, and for aqueous solutions and other bodies usually positive out- ward, and due purely to voltaic contact. If this view is cor- rect, i. e., if air in contact with pure water is invariably negative by contact action no matter whether the surface is plane or markedly convex, and if air in contact with salt solu- tions is invariably positive, the solution being negative, then it is the negatively charged nucleus (solution) which persists and the positively charged nucleus (pure water) which is fleeting or virtually non-existent. It follows, therefore, that condensa- tion with subsidence is equivalent to a removal of negative electricity provided the air charge is not simultaneously removed. Of. § 5. Brown University, Providence, R. I. * Lenard, Wied. Ann. , Xlvi, pp. 584-636, 1892. 234 Hmerson—Corundum and a Graphitic Essonite. Art. XX VIII.—Wote on Corundum and a Graphitic Essonite Jrom Barkhamsted, Connecticut ; by B. K. Emerson. SoME years ago I received from Mr. W. E. Manchester of Pleasant Valley in Barkhamsted who is well acquainted with the mineralogy of the region, a large block of a heavy bluish black rock which proves to be corundum, and several speci- mens of a very peculiar large garnet which are penetrated by quite thick sheets of graphite. The accompanying rock, which seems to be the country rock and which occupies a large area, is a coarse mica schist, which in a northwest direction for two miles abounds in smaller garnets 2-5™™ across, of red color, accompanied by dark red- dish brown staurolite crystals an inch across, and also cyanite in blackish crisscrossed blades an inch wide and two inches long. Near where the cyanite occurs there comes in above it a fibro- litic gneiss which I have, farther north, associated with the Algonkian. This latter rock contains layers, an inch thick ; of a compact or finely fibrous fibrolite (faserkiesel) containing many large grains of magnetite. The mineral proves under the microscope to be made up of almost pure matted fibrolite needles. Garnet.—The remarkable garnets occur in well-formed dode- cahedrons above two inches in diameter and extend over a broad area forming a very coarse continuous drusy surface, some erys- tals rising so as to show almost all their faces, others fused into large groups which rise several inches above the surface of attach- ment. They do not, however, present the aspect of crystals which have grown freely into a cavity, since the faces are not pol- ished and continuous but rather dull and often deeply exea- vated with deep and irregular cavities from which some mineral has been removed by solution. In the least weathered crystals there are still large grains of included calcite visible, and we may assume that the mineral which has been removed from the depressions was calcite, that the whole broad surface of great crystals has grown from a base of mica schist up into a bed of crystalline limestone, which has been removed by solu- tion from the surface of the’ crystals. The character of the crystals agrees with this derivation. They are pale honey-yellow to almost colorless, agreeing in tint and general appearance closely with the crystals from Gatineau, Canada, except that they are simple dodecahedrons, are much larger and lack the polished faces, though this may be due to a subsequent weathering. They are doubtless a quite Emerson—Corundum and a Graphitic Essonite. 235 pure essonite. Because of this weathering they have now a dull gray and unattractive appearance, and this is increased by the fact that about half the surface of each crystal face is occu- pied bya dull black minerai in irregular blotches, arranged in a somewhat pegmatitic way. This sometimes increases in amount so as to occupy almost the whole surface of each face of the large crystals, and these faces are then irregular, and in the great mass of aggregated crystals where this is car- ried to the extreme it is continued up to a rather sharp plane beyond which the crystals are quite free from the black min- eral, and this plane passes through the middle of the largest crystals. In a section cut through a crystal where the surface was almost all black, the dark color disappeared rather suddenly about half an inch from the surface, but the dark mineral penetrated in narrow wedge-like plates far into the compara- tively pure garnet. The mineral is a pure soft graphite, especially in the wedge- like projections last mentioned, or a very fine granular mix- ture of graphite and garnet over the gray areas. When a fractured surface on a slide is examined with a lens it has nowhere a homogeneous or crystalline appearance, but looks more like a fine-grained white aplite, and this character is maintained under the microscope which shows a brightly polarizing mosaic in which one can, with difficulty, detect here and there a nonpolarizing grain of garnet. Large grains or phenocrysts of twinned calcite are very abundant, and the rest of the field is mostly made up of large feathery aggregates of coarse columnar wollastonite, full of minute blebs of quartz and quite large anhedra of diopside. It is remarkable that such large well-formed crystals have so small a fraction of garnet in their composition. It is only at the surface that a thin Jayer of nearly pure garnet can be found. Corundum.—The corundum block is from a very pure bed about two and a half inches thick, with the glistening luster of the Ceylon massive emery. It is a dark blue over most of its surface with small irregular patches of pistachio-green. The specific gravity of the rock is 3°64. It scratches topaz. Under the microscope the rock is made up of stout colorless grains two to four times as long as wide, with straight, dis- tinct, almost cubical fracture lines. These grains have a very low polarizing color, gray to white of the first order. They have a much higher index of refrac- tion than the cyanite which is scattered in them, in porphyritic plates. 236 Emerson—Corundum and a Graphitic Essonite. The cyanite is in rather square blades with good cleavage and basal parting and around its borders has broken up into an alteration product. The whole field is filled with coaly matter in trains, aggre- gates and groups of round balls which often occupy the center of the corundum grains. This carbonaceous matter has plainly been introduced in an oily or tarry condition and has been inspissated in place, and the abundant graphitic matter in the garnet gives indication of the same origin. Amherst College, Amherst, Mass. THE AMERICAN JOURNAL OF SCIENCE [FOURTH SERIES. |] Arr. XXIX.—An Experimental Investigation into the Exist- ence of Free Ions in Aqueous Solutions of Electrolytes ; by Juzius Oxsen.* Van’t Horr in 1887+ showed that the gas laws of Boyle, Gay-Lussac, and Avogadro, hold also for dilute. solutions. From considerations of osmotic pressure, theoretically and experimentally, he was able to apply Avogadro’s law to solu- tions, and gave it as follows: “The pressure which a gas exerts at a given temperature, if a definite number of molecules is contained in a definite vol- ume, is equal to the osmotic pressure produced by most sub- stances under the same conditions, if they are dissolved in any given liquid.” ; These laws may be combined in the well known expression PN =P which holds for most substances, where P is the osmotic pres- sure and V, T, and R, as in the gas law, are volume, absolute temperature, and = a for a perfect gas, respectively, and in- cludes Avogadro’s law if we consider kilogram-molecules of the substances, as Horstmann has shown. Van’t Hoff found that the above expression held for most substances, but there were many important exceptions. These exceptions were the acids, bases, and salts; in these the osmotic pressures were greater than the law required. In other words, he found that the solutions with abnormal osmotic pressures were the electrolytes. He accordingly introduced into the expression the coeflicient ¢ and wrote it Ba Vee oe ava * An abstract of a thesis presented to the Graduate Faculty of Yale Uni- versity for the degree of Doctor of Philosophy. + Zeitschr. Phys. Chem., i, 4815 1887. Am. Jour. Sc1.—FourtuH Series, Vout. XIV, No. 82.—OctToBErR, 1902. 17 238 J. Olsen—Investigation into the Existence of This coefficient would be one for “ideal” solutions and greater than one for the acids, bases and salts. Arrhenius* showed, also in 1887, how these exceptions might be explained; and thus the law hold for a// substances. The osmotic pressure, other things being equal, depends upon the number of particles present in a given volume of the solu- tion, in the same way as the pressure of a gas depends upon the number of its particles. If then the osmotie pressure is too great, there must be more particles present than were put in. These substances must therefore be dissociated, i. e., the molecules split up into two or more parts. Arrhenius rea- soned in this manner. This same assumption had been made use of to explain the abnormal pressures of some gases; but on account of the chemical objections had not before been applied to solutions. Arrhenius accordingly brought forth again the electrolytic theory of Clausius, and established it, seemingly, by showing how to caleulate the amount of dissociation. Clausius had believed that “some of the molecules of an electrolyte are dissociated into their ions, which move about independent of each other.” During electrolysis these mo- mentarily free ions would be guided to their respective poles. According to this theory there is no direct decomposition of the electrolyte by the current, as was held by Grotthiiss in his theory. It has been shown since the time of Grotthtss that electricity moves with the same ease in electrolytes as in metals, so there is no place for such work as decomposition. From the activity coefficient (a), which he considers the ratio of the actual molecular conductivity to the maximum con- ductivity, i. e., the conductivity at infinite dilution, Arrhenius proceeds to show how to determine the coefficient 2 of the formula, and thus test the theory. By a comparison of the lowering of the freezing point of a liter of water, in which a gram molecule of the substance is dissolved, and 7 as caleu- lated from the conductivity method, he found the agreement to within tHe limits of experimental error. The theory has since been tested by a great many men, by the method of the lowering of the freezing point, the rise of the boiling point, osmotic pressure, conductivity, etc. There are seemingly some exceptions as shown by Kahlenbergt and others, but the preponderance of evidence is certainly in its favor so far. Some of these exceptions may be due to the somewhat limited knowledge we have of the true composition of some substances. And the law has its limitations, in the same way as the gas laws, and holds only for dilute solutions. The theory, at least, explains a great many phenomena that cannot be explained, at present, by-any other means. * Tbid., i, 631, 1887. + Am. Jour. Phys. Chem., June, 1901. i a Free Ions in Aqueous Solutions of Electrolytes. 289 No direct experimental proof was attempted until Ostwald and Nernst,* m 1889, performed the following experiment. It will be given substantially in their own language. A glass tube about 30 or 40™ in length, provided with a stopcock, was drawn out to a fine capillary at one end. The tube was then partly filled with mercury and hung upright, with the capillary in a solution of dilute sulphuric acid. By suction at the upper end the mercury was drawn up and the sulphuric acid after it. When at a convenient height, about the middle of the capillary, the stopcock was closed and the liquid thus held in place. A platinum wire fused into the tube connected with the mercury. A large glass flask was now filled with dilute sulphuric acid and insulated by placing it on a disk of hard rubber. The outer surface of the flask was coated with tinfoil and its neck varnished with shellac. The contents of the flask were con- nected with the sulphuric acid into which the capillary tube dipped, by means of a wet string. The positive pole of a small electric machine was brought in contact with the tin- foil, and the mercury of the capillary electrometer connected with the earth. As soon as the electric machine was set in motion the mer- eury of the electrometer rushed up and at the same time bub- bles of gas separated, which broke the thread of mercury in a number of places. This is the explanation given.—By charging the outer cov- ering of the flask with positive electricity, the negative elec- tricity on the inner side would be attracted and held, while the positive would be repelled. The latter would go by the wet string to the capillary electrometer and then by the plati- num wire tothe earth. There is no closed current; the entire movement of electricity is produced by induction. This proves, they say, that free ions were present and that they moved. They performed several other experiments, but all are on the same principle, and the same conclusions are drawn. There seems to be good reason for the belief that the con- clusion arrived at does not necessarily follow, but that we need further proof. The potential of an electric machine is very high and the flask they used in connection with the capillary electrometer is really a condenser. As no substance insulates absolutely there must be in such an arrangement some current, and in such a restricted path there is a possibility of a considerable difference of potential. They do not say that the potential difference, between the two ends of the capillary electrometer, was measured. If this exceeded about 1°22 volts there was electrolysis and consequently a formation of gas bubbles. * Zeitschr. Phys. Chem., iii, 271, 1889. 240 J. Olsen—Lnvestigation into the Kxistence of J. H. Pratt* shows that no current passes through a capil- lary electrometer below 1:22 volts. If no current can pass through a Lippmann electrometer before about the electrolytic limit of decomposition is reached, then this instrument is not a good one for this experiment. In order further to test the capillary electrometer when connected for some time to voltages below 1:22, 1 made an instrument as follows: A glass tube about 15°" in length was drawn to a capillary at about 5™ from one end. Into this shorter portion a platinum wire was fused. The tube was then filled with mereury and dilute sulphuric acid and inverted into a beaker containing dilute sulphuric acid and mereury. A cork was put on the upper end, and by releasing this a little the boundary between the mereury and sulphuric acid could be brought into the capillary. A space was left above the mercury so that it could recede when connected up to a Daniell. * The Stereographic Projection and its Possibilities, loc. cit., p. 12. 282 Penfield—Solution of Problems in Crystallography y and 7; compare figures 6 and 8. The angle a was measured by means of the stereographic scale on the diameter 1 to 2, figure 30, and found to be 98° 25’, calculated 93° 14’. Sim- ilarly 8 was measured on the diameter 4 to 5, and found to be 116°, caleulated 115° 56". To measure 7 and t, a great circle at 90° from ¢ was first constructed.* The supplement of 7, from 6 to 7, was then determined as 88° 55’ by means of the small circle protractor, giving as the value of 7, 91° 5’, caleu- lated 91° 12’.. In like manner the are from 7 to 8 was meas- ured, giving 32° 5’ as the value of r. On still a third sheet, shown in figure 32, the angles a, 8 and 7 were plotted, and also t, the latter determining the length of the brachy axis, a=0°636, calculated 0°635. It is still necessary to make use of the fifth fundamental measurement, from 6 to e, in order to determine the length of the vertical axis. By means of a small circle about 6, figure 30, the position of e, on the great circle b,c, was located, and a great circle through 100, e and 100 de- termines z. The value of z, measured on the diameter from 2 to 8, was found to be 45° 45’, and when plotted as shown in figure 32, the length of 2c was found to be 1-095; hence c=0°5475, calculated 0°550. The value obtained directly from z in this case is 2c, because the symbol of e is 021. Having located, as in figure 30, the poles 6, m, 100, WZ, ¢— and e, and also. fand z from figure 31, the remaining forms of the crystal were easily identified by means of zonal relations and the measurement of a few angles. The construction of the zones shown in figure 30 would have proved a laborious task had it not been for the great circle protractor. This was used not only for determining the zones, but, far more impor- tant, its graduation furnished the means of getting the radii of the circular ares from scale No. 1 of the sheets. Meas. Cal. Error Cal, 001A 201, 41°° 30’ 41° 28’ + 2 Cag, . O01LA 84 45 34 46 — 1 CA. | Ot 01: 51 40 bil 26 +14 cay, 001A 201, 81 30 Si +16 CAD, (Ol yn1 14, 33 pao 33 17 — 7 eR a. 40Ol ALT, 34 tae 34 10 +25 - Cnn AOU AL, 5d CahO 5A 17 — 7 Co, (00k F1b, 58 00 512 + 8 cau, O001A221, 85 00 84 50 +10 enka UOL,A0b1, T 20 514 MO +10 can, 001,021, 47 00 46 46 +14 Cade. JMG 18 . 55 18 38 +17 O 207, 7) ONO 52020 ek Wl + 9 b nn, OWA 34 10 34°20 10 On”G,- O10> 88 05 38>) .1G —11 Aw, O10A aishe, De 38 42 +13 * The Stereographic Projection and its Possibilities, loc. cit., p. 18. ee ae SS ae =e"! by Means of Graphical Methods. 283 - A list of measurements made with the small circle protractor is given in the table on the foregoing page. The average of the errors is 11’, with errors of more than a quarter of a degree in only three instances. In figure 30, the angle between the great circles b,c and 6,p determines » (compare figures 6 and 8), which was found to measure 29° 25’. The angle »v, plotted from unity on the @ axis, as shown in figure 32, gives another method for determining the length of the ¢ axis; in this case ¢@ was measured as 0°545, caleulated 0°550. CoNCLUSION. In the foregoing pages the attempt has been made to indi- cate not only the methods of plotting problems in the several systems, but, also, to give an idea of the accuracy of the results thus obtained. In judging the accuracy of the results it must be kept in mind that the scale employed was quite small, the engraved circle being only 14°™ (54 in.) diameter. Each prob- lem presented was worked out from fundamental measure- ments, as would have been the case if done by numerical cal- culation, and the results indicate that for all practical pur- poses graphical methods are in every way satisfactory. The lengths of axes have frequently been obtained correctly to the third place of decimals, and never varied more than one in the second place, and measurements of arcs and angles by the stereographic protractors have been reasonably close to the calculated values in all cases. After becoming familiar with the principles involved in dealing with the projection—and they are not difficult to understand—any problem may be worked out without the use of. prescribed formulas, or tables of any kind, and this the writer believes is one of the great advan- tages of the method. Then, too, it is a very simple step to proceed from a graphical to a numerical solution, for the prin- ciples involved are identical, and it is only necessary to apply the formulas of spherical and plane trigonometry in order to obtain the desired results by calculation. The writer has never made use of formulas for solving even the most complex prob- lems of crystallography, other than those needed for the gen- eral cases which arise in dealing with spherical and plane triangles, and it is his belief that the too general use of pre- seribed formulas is, if anything, a hindrance to true progress in crystallography. Graphical methods will also be found to have very decided value as giving a ready means of checking the results of numerical calculations. During the past two years, since they have been in use, numerous cases have arisen where mistakes in calculation have been made, at times amounting to less than a degree, but they have been almost 284 Penfield—Solution of Problems in Crystallography. instantly detected by applying the protractors to the stereo- graphic projections. Generally it has been found that mis- takes were due to errors (carelessness, perhaps, is a better term) in such simple processes as addition and subtraction. In an earlier communication* a description was given of blackboard appliances which have proved most useful for dem- onstrations of the stereographic projection on a rather large scale before a class. Thus, in the discussion of any problem which may arise, a projection may be made in a few minutes, from which the zonal relations, symbols and angles of the forms may be determined. As a demonstration of the prac- ticability of the method, a projection of pyroxene, like figure 25, page 277, was constructed from fundamental measurements, and the following determinations made, the time consumed being nineteen minutes: Given, mA mm’ =92° 50’; cA p=88° 49’ and aAc=TA4® 10’. Axes:determined; a :6::.¢ =:1-ils: 1:2:0-585: ; Axes calculated; a: 0::'c = 1-092 21 08a ' Angles. Meas. Cal. Angles. Meas. Cal. i Cy VO aA OOT=79": 79°, 9! 0A 0, 221 a 29184) 4a crd, 001A101=31 31 20 CA0, OO1LA321=65 65 21 PAD, VILAI1II=48} 48 29 app, 100, 111=5ae Sas Sas. 111 Adi 595 59041 GAS, 100A 111=763 ieee Cas, 001A TII=494 42-2 a2A0, 100, 221=625. soles It should be stated that the foregoing problem was exe- cuted with blackboard crayon, and with beam-compass and scales graduated to every fifth degree only. Finally the writer would state that in his own laboratory the graphical methods have proved most serviceable, and it is be- lieved that by means of them a far better msight into mathe- matical crystallography and the meaning of zonal relations and angles has been gained by the students, than when other methods were employed. There is no wish to discourage numerical calculations; such must be made, and facility in making them must be acquired, but the graphical methods, if properly interpreted, are, if anything, a decided help, for they give meaning to the calculations, which, far too often, are made by prescribed formulas, wholly meaningless to the average student. * The Stereographic Projection and its Possibilities, loc. cit., p. 140. Sheffield Laboratory of Mineralogy and Petrography, Yale University, New Haven, May 1902. a ewes! eer oe © Gooch and Blake— Estimation of Bromic Acid. 285° Arr. XX XI.—The Estimation of Bromic Acid by the Direct Action of Arsenious Acid; by F. A. GoocH and J. C. BLAKE. 3 [Contributions from the Kent Chemical Laboratory of Yale University—CXI. ] In a former paper from this laboratory* it has been shown that iodic acid may be reduced quantitatively by arsenious acid. In the work of which the present paper is an account the attempt has been made to apply arsenious acid similarly to the quantitive estimation of bromic acid, according to the equation 3H,AsO,+HBrO, = 3H,AsO,+ HBr. In the following series of experiments, made to discover the limits within which regularity of action might be expected, definite amounts of arsenious oxide dissolved in acid potassium carbonate were mixed with measured portions of a solution of potassium bromate, sulphuric acid was introduced in the amounts indicated, and, after standing either at the ordinary temperature, on the steam-bath or at the boiling temperature, potassium acid carbonate was added and the arseniate remain- ing was titrated with iodine to color, the indication being confirmed by addition of starch. The conditions of acidity, the excess of arsenious oxide, the dilution, the time of action, and the temperature were varied within wide limits. The potassium bromate for this particular series of experiments was thrice recrystallized from water, dried at 110°, and made up in solution containing 2°8 grms. to the liter. Of this solution 25 or 50° were measured out for each experiment. TABLE I, Volume not exceeding 200°™%, H.SO, As2O3 Error in KBrO; As2,0O; (£1): ~.'Fime of As2Os oxi- terms of taken. taken. taken. diges- unchanged. dized. KBrOs. grm. erm, em*. tion. erm. grm. erm. Heated at the boiling temperature. 0°1400 0°4950 10 30 min. 0°2476 0°2474 0°0008— 071400 0°4950 10 30° “ 0°9480 0°2470 0°0010— 0°1400 0°6188 10 20 SG LOS 0°2480 0°:0006— 0'1400 0°7425 8 25 1/59 OA GAT 0°2484 0°0003— 0°1400 0°7425 8 ZK Vek Se: 04943 0°2482 0°0004— 0°1400 0°6188 7 20 ei O3704 0°2484 0°0003— - ( 0°1400 0°6208 20 “ 0°3720 0°2483 0°:0004 — * Gooch and Pulman, this Journal, xii, p. 450 (1901). Am. Jour. Sci1.—FourtH SERIES, Vou. XIV, No. 82.—OcrTossr, 1902. 20 . ‘286 Gooch and Blake—Estimation of Bromic Acid KBrO; taken. grm. -0°1400 071400 0°1400 [ 0-1400 0°0700 0°0700 0°0700 0-0700 0:0700 0:0700 0°0700 0°0700 0°0700 0:0700 0-0700 0-0700 0:0700 0°0700 0°0700 0-0700 0:0700 0-0700 0-0700 [ 0-0700 071400 0°1400 0°1400 0°1400 071400 071400 071400 071400 [ 0-0700 0°1400 0°1400 0°1400 0°1400 01400 As.Os taken. erm. 0°6188 0°4950 0-4950 0°4950 0°2475 0°2475 0°2475 0°2475 0°2475 0°2475 0°1584 0°1584 0°1584 0°1584 071881 0°1881 0°1881 0°1881 0°1881 0°2475 0°2475 0°2475 0°2475 0°2475 0°4950 0°4950 0°4950 0°4950 0°4950 0°4950 0°4950 0°4950 0°2475 0°4950 0°4950 0°4950 0°4950 0°4950 TABLE I—COontinued. Volume not exceeding 200°™°. H.SO.4 As2O3 (1 >i)" Aimeot As2O3 oxi- taken diges- unchanged. dized. cms. tion. grm. grm. Heated at the boiling temperature. a) 15 min. 0°3712 0:2476 Bb Lb = *'O-2880 M024 7m 3°5 15 “ -0°2482 0°2468 2°5 LT t OFDEQO 0°2321 i) Peto ess OueAO 0°1235 ) Lo O39 0°1236 9) nS Se ORL Qos ODRaE7. 5 15 .“- .0°1244 Onan 5 LOT ro dee 0°1236 5 DO eh itastanl 0 8 be 21S 97 0°1238 5 LQ ee O:0nee 0°1239 5 TOO OOOaa 071227 O 10. 500356 0°1228 5 10°. *2) 2O°0S5s 0°1231 8 10 “ ~0:0649 0°1232 5 10 ‘* 0°0640 0°1241 5 10 ‘* 0:0649 0°1232 5 5 O06S2 0°1229 5 5 “ °0:0652 0:1219 2°5 10,2, ¢8> “O:238 0°1237 | 2 LOc. MS S3Ob285 0°1240 TLS 70 3 Sede 4D 0°1233 | 1515) dO 55%, HOS Ag 0°1235 11D Da WOO 0°1175 Heated on the steam-bath —80°. i0 150 min. 0°2476 0°2474 10 150 2 FJ 0e24g6 0°2474 + 240 “ 0:2478 0°2477 = 240 “ 0°2475 0°2475 4 180 “ 0°2472 0:2478 a 180 ‘ 0:2470 0°2480 3°O 90"! nO 2475 0:2475 3°5 9020S “RO QAT6 0°2474 1715." BO SCO 1622 0°0853 Digested at the ordinary temperature. 4: 46 hrs. 0°2480 0:2470 3°5 AY “o> 0°24 75 0°2475 3°9 41° * 02470 0°2480 3°5 17 ~ "5, 0:2490 0°2460 3°5 17 072492 0°2458 Error in terms of KBrO; = erm. 0:0008 — 0-0010—. 00011 — 0:0097— |] 0:0005 — 00004 — 0°0015 — 0:0007— 0:0004—. 0-0003 — 0:0003 — 00009 — 0:0009— 0:0007— 0‘0007~—— 0°0002 — 0:0007— 0:0008— 0:0008— 0:0004 — 00002 — 0°0006 — 0:0005 — 0:0038— | 00008 — 00008 — 0:0007— 00008 — 0°0006— 0°0005 — 60008 — 0:0008— 0°:0217— | 0°0005— 0°0008 — 0°0005— 0:0016— 0:0017— a by the Direct Action of Arsenious Acid. 287 An examination of these results discloses the fact that for conditions varying within a rather wide range the oxidation of the arsenious oxide reaches a fairly definite limit. The bromate effects practically the same proportionate oxidation of arsenious oxide in a volume of 200° or less, whether the sul- phuriec acid of half-strength present amounts to 3°5°™ or 10™, and whether the time of digestion is 15 minutes or 30 minutes at the boiling temperature, one and one-half or four hours on the steam-bath, or two days at the ordinary temperature. Setting aside those experiments in which the addition of acid did not exceed the equivalent of alkali carbonate present by more than 1°’, the average absolute variation from theory of the entire list of forty-two experiments amounts to 0:0007— grm. in terms of bromate, individual variations departing from the average by about the same figure. The obvious meaning of this fact seems to be that the slight error is due to impurity in the potassium bromate employed and not to incomplete oxidizing action on the part of the bromate. In the following series of experiments another preparation of bromate was employed, and its value was fixed by reduction with acidified potassium iodide and titration of the iodine set free according to the method formerly proposed by Kratchmer.* The rate at which the action proceeds, according to the equation 6HI+HBrO, = HBr+3H,0+1,, has been investigated by Ostwald,t by Noyes,t and by Judson and Walker.§ Time of action, proportion of iodide to bromate, excess of acid, and dilution are all, within limits, determining factors in the reaction; but in the analytical process it is usually assumed that the reaction goes soon to completion if free acid and a moderate excess of potassium iodide are present. In the following table are recorded the results of experiments in which measured amounts of standard solutions of potassium bromate (approximately 2°8 grms. to the liter) were treated with potassium iodide and hydrochloric or sulphuric acid for definite times in glass-stoppered bottles, the iodine liberated being determined by titration with sodium thiosulphate standardized against nearly decinormal iodine of value fixed by comparison with decinormal arsenious oxide dissolved in acid potassium carbonate. * Zeit. Anal. Chem., xxiv, 546 (1885). + Zeit. Phys. Chem., ii, 127 (1888). t Zeit. Phys. Chem., xix, 599 (1896). $ Jour. Chem. Soc., Ixxiii, 410 (1898). 288 @ KBrO; = Iodine taken. erm. ) 071410 ) 071410 8) 0°1400 ) 0°1400 ) 0°1400 ) 071408 ) 01408 ) 0°1408 ) 0°1400 ) 2) 0:1400 3) 01400 (14) 0°1400 (15) 071400 (16) 0:1400 (17) 0°1400 (1 (19) 0:1400 (20) 01400 8) 0:1400 (21) 0:1400 (22) 01400 considerable. reaction is very incomplete. taken. taken. erm. 0°6423 0°6423 0°6378 0°6378 06378 0°6416 0°6416 0°6416 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 0°6378 Pasun 1. A Time of KI H.SO, stand- (i), ine, orm, pce. Thrs: uy 5 none ik 5 none 3 5 4 3 5) oo 3 5 4 3 5 22 3 5 29 3 5) 22 3 hues and 3 YA > 3 2°) 4 3 ee > 3 0:5 4 B Het Sp. cris cem?, 3 8 4 Bie 548 4 Bn ate 2 3 4 4 a 4 4 3 4 4 3 4 if 3 4 li 3 4 l Approxi- mate volume. cm®, 150 200 100 100 100 100 100 100 100 100 ,100 100 100 100 100 100 100 100 100 100 100 100 Todine found. grm. 0°6223 0°5929 0°6343 0°6329 0 6329 0°6396 0°6364 0°6381 0°6340 0°6336 0°6336 0°6343 0°6331 0°6336 0°6329 0°6336 0°6336 0°63338 0°6340 0°6336 0°6333 ‘0°6336 Gooch and Blake—Estimation of Bromic Acid Error in terms of KBrO; grm. 0°0044 — 0°0108— 0°:0008 — 0:0011 — 0:0011— 0°0004 — 0:0011— 0:'0008 — 0:0008— 0°0009— 0:0009— 0°0008— 0°0010— 0:0009— 0.0011— 0°0009— 0.0009— 0°0010— 0°0008— 0:0009— 0°0010— 0°0009— In experiments (1) and (2) the excess of potassium iodide was only about 20 per cent over the amount demanded by theory, the time of standing was only the few minutes required for the manipulation of ‘the process, and the dilution was It is obvious that under these conditions the On the other hand, a glance at the table makes it evident that the oxidation in all other experiments, whether in A or B, proceeds to practically the So it appears that the variation in the amount of acid above the minimum, the kind of acid (whether sulphuric or hydrochloric), and the time above the minimum half-hour, within the limits defined, are same point, showing similar errors. without apparent effect upon the reaction in the presence of the amount of potassium iodide used, approximately four times by the Direct Action 6f Arsenious Acid. 289 the amount required by theory. The balancing error due to the evolution of iodine by the action of atmospheric oxygen upon the acidified solution of the iodide was found by experi- ment to vary with the strength of the acid and the time of exposure, from 0°0001 grm. to 00003 grm. expressed in terms of the bromate, and these values are not greater than the differences observed between parallel determinations of the same sort. Probably, therefore, all the errors as shown in the table should really be increased a trifle to approximate the truth, notably those of the experiments allowed to stand the longest period, twenty-two hours. The average apparent error of the process as applied to this particular sample of bromate is 0°0009- grm.; and 2°5™* of sulphuric acid of half-strength (1:1) or the equivalent amount of hydrochloric acid, 4™ of the acid of sp. gr. 1:18, in the presence of about 3 grms. of potassium iodide, complete the action within a half hour, at a dilution of 100, as far as it will go under any of the conditions tried. The phenomenon noted by Ostwald,* that small amounts of hydrochloric acid tend to force the reaction more rapidly than equivalent amounts of sulphuric acid, does not appear in these experi- ments, no doubt because the action was pushed to the limit by the smallest amount of the weakest acid employed. The error of deficiency shown again appears to be due to impurity in the sample of bromate rather than to incomplet- ness of the reaction. If the reaction were incomplete it would be natural to look for the cause in the possibility of the inhibiting influence of the iodine set free,t+ but it was found in three parallel experiments that the introduction of ‘5 grm. of free iodine dissolved in potassium iodide failed to influence the error appreciably. For the present pur- pose, however, the absolute purity of the bromate is not a matter of moment, if, as seems to be the case, Kratchmer’s reaction indicates its value with accuracy, as the basis of experi- mentation. It seems safe to assume, then, that the average result of experiments (8) to (22) will give a very fair valve for the sample of bromate investigated. That is to say, the experiments show an average deficiency in bromate amounting to 0°0009 grm., or to 0-64 per cent. Portions of this bromate were taken for reduction by arsenious acid. Solutions not exceeding 200° in volume, containing the bromate and a considerable excess of arsenious oxide acidified with sulphuric acid of half-strength, were boiled for periods varying from ten to forty-five minutes, neutralized with potassum acid carbonate, and titrated with iodine. The resnits are shown in Table III. = koe: cit., p. 151. + Judson and Walker, loc. cit., p. 411. 290 Gooch and Blake—Estimation of Bromie Acid Tas eE III. Error in KBrO; As,O; H.SO, Time As.O3 As,O3 terms of taken. taken. (£21): in unchanged. oxidized. KBrOs. erm. erm. cm*®. minutes. grm. erm. grm. ( L)yO°eTOk: 01881 10 0°0661 0°1220 0°0014— ( 2) 0:0701 01881 10 0°0650 0°1231 0°0009— ( 3) 0°0701 0°2475 10 0°1232 0°1248 0°0002— ( 4) 0.0701 0°2475 10 0°1236 0°1239 0°:0004— ( 5) 0°0701 0°2475 25 0°1234 0°1241 0°0003— ( 6) 0°0701 0°2475 0°1234 0°1241 0.0003— ( 7) 071402 0°4950 15 02479 02471 0°0012— ( 8) 071402 0:4950 15 0°2476 0°2474 0°00 LO— ( 9) 071400 06188 20 0°3708 0°2480 0°0004— ( 20 0°3710 0°2478 0°0005— ( 20 0°3706 0°2482 0°0003— ( 30 0°3708 0°2480 0:0004— ( 45 0°3711 0°2477 0°0006— 10) 071400 0°6188 11) 0:1400 0-6188 12) 0°1400 0°6188 13) 071400 06188 7 oT wT ST Tr Oo W& OFT OF St ST OT or bo Or Here again, as in the experiments of Table I, the indications of the process of reduction of the bromate by arsenious acid, point to a slight deficiency in the oxidizing power of the bromate. The mean deficiency, 0°0006 grm., differs from the indications of the process of reduction of the same sample by the potassinm-iodide method by about 0:0003+ grm. The question now arises as to what is the impurity in the bromate. In a product recrystallized several times, and in one in which no chloride can be detected, as was the case with the bromate of these experiments, the impurity most natural to look for is potassium chlorate, which, might resist removal in the process of purification by recrystallization. The pre- paration of bromate upon which these last experiments were made was therefore tested by igniting it and treating the resi- due with potassium bichromate and sulphuric acid, volatiliz- ing and collecting any chloro-chromic anhydride thus formed, and converting the last into lead chromate.* Traces of chlorine were thus found, which, not appearing in a similar test upon the unignited bromate, must have had their origin in chlorate intercrystallized with the bromate. Ina former paper from this laboratory+ it has been shown that a chlorate may be determined by adding to it in solution potas- sium iodide in known amount and an excess of an arse- niate and sulphuric acid, boiling the mixture between definite limits of concentration, determining by titration with iodine the amount of arsenious oxide produced, and calculating the amount of chlorate present, from the difference between the amount of arsenious oxide thus produced and that which * Gooch and Brooks, this Journal, xl, p. 287 (1890). +Gooch and Smith, this Journal, xlii, p. 220 (1891). by the Direct Action of Arsenious Acid. 291 should be produced if the whole amount of iodide added were allowed to act upon the arseniate alone. There appears to be no reason why’a bromate treated by this process should not leave a similar record of its oxidizing power. A mixture of bromate and chlorate should, therefore, in this process, leave a record of the full amount of oxidation of which both together are capable. The following table contains the account of experiments made in this manner upon the sample of bromate the action of which in the iodide method and in the arsenious acid method is recorded in Tables II and ILI. Papi 1V- (H2SO.) (1:1) 20°™3; initial volume 105 to 170 ; final volume 35°™°, Iodine corre- Ivalue sponding to Jodine corre- Error in KBrO; H.KAsO; of KI As203 sponding to terms of taken. taken. taken. produced. KBrOs. KBrOs. erm. erm. erm. erm. erm. erm. (1) 0:0700 2 0°4146 0°0948 0°3198 0:0002+ (2) 0:0700 2 0°4146 0°0954 0°3192 0°0000 (3) 0°0700 2 0°4146 0°0969 0°3177 0°0003— (4) 0:0700 2 0°4146 0°0975 0°3171 0°0004— (5) 0°1400 2 0°7832 0°1458 0°6374 0°0001— 6) 0°1400 2 0°7832 0°1465 0°6569 0°0002— + 0°1400 2 0°7832 0°1462 0°6370 0°0002— The mean error of these determinations, in which: all oxidizing material is calculated as bromate, is not far from 0-0001— grm. In the case of still another preparation of potassium bromate, made by acting with commercial bromine on potassium hydroxide, crystallizing and _ recrystallizing several times, determinations by means of arsenious acid and’ by the arseniate- iodide process resulted as shown in the following statement : TABLE V. B Arsenious Acid Method. (Volume not exceeding 100°™?.) AsoO3 As2O3 Error in KBrO; As.O3; H.~SO, Time un- Oxi- terms of taken. taken. a in changed. dized. KBrO; erm. erm. erm. minutes. erm. erm. erm. At the boiling temperature. mea,O4 § O°2475 5 10 O° E241 0°1234 0°0010— m0704 0°24'75 5 15 0°1239 0°1236 0:0009 — 0°0704 0°2475 oe 15 — 0°1256 0°1239 0°0007— 292 Gooch and Blake—Estimation of Bromic Acid. TABLE V—Continued. 1 Arsenious Acid Method. (Volume not exceeding 100°™3,) As2O3 As2Os Error in KBrO; As2,O; H2SO, Time un- oxi- terms of taken. taken. Cs) in changed. dized. KBrO; erm, erm, erm. minutes. erm. erm. erm. On the steam bath,—80°. 0°0704 0°2475 5 30 0°1241 0°1229 0°0015— O°0704 0°2475 5) 30 0°1246 0°1234 0°0010— At atmospheric temperature. 0:0704 0°2475 9) 10 -0°2066 0°0409 0°0474— 0°0704 0°2475 5 10 0°1991 0°0488 0°0426 — O°0704 0°2475 5) 30 0°1533 0°0922 0°0185— 00704 0°2475 5) 60 0°1231 0°1244 0°0004 — 00704 0°2475 i) 120 0°1242 0°1233 0°0011— 0°0704 0°2475 5 120 0°1238 0°1237 0°0009 — B Arseniate-Iodide Method. (H2SO,) (1:1) 20°™* ; initial volume 110°™?; final volume 35°™3, Iodine corre- sponding to Jodine corre- Error in KBrO; H2KAsO, I value of As2O3 pro- sponding to terms of taken. taken. KI taken. duced.. KBrOs. KBrO3. grm. erm. erm. erm. erm. erm. 0°0704 2 0°3812 0°0607 0°3205 0°0001 — 0°'0704 pi 0°3812 0°0588 0°3224 0'0003+ 0°0704 2 0°3812 0°0595 Ors2ay 0°0001+- 0°0704 2 0°3842 0:0590 0°3222 0°0002+- 0'0704 2 0°3812 0°0615 0°3197 0:0003 — 0°0647 2 0°3812 0°0839 0°2973 0:0004+ The mean error of the arseniate-iodide process applied to this particular sample of bromate is 0°0001+ grm. in terms of bromate ; the arsenious acid method shows a mean deficiency of about 0:0009 grm. for the smaller amount of bromate employed, if, as is obviously reasonable, those results are omitted from the averages which were obtained by standing at the ordinary temperature for periods less than one hour. - It appears, therefore, that the deficiency in the indications of the iodide process and the arsenious acid process are satisfactorily accounted for by the presence in the bromate of traces of chlorate; and that the oxidizing power of a bromate may be determined by boiling it in solution with a known excess of arsenious oxide and an excess of sulphuric acid, and determining the amount of arsenious oxide remaining unchanged. A chlorate, as we have found by direct experi- ment, is scarcely affected by this treatment. os Speyers—Solubilities of Some Carbon Compounds, ete. 298 Art. XXXIL.—Solubilities of Some Carbon Compounds and Densities of their Solutions ; by CLARENCE L. SPEYERS. At the present time we are more or less inclined to find in solution an action corresponding to vaporization, and as vapori- zation under ideal conditions is generally considered indepen- dent of the contents of the space into which the substance volatilizes, chemical action of course being excluded, so in forming dilute solutions we generally expect ‘the act of solution to be independent of the medium into which the solute passes, that is, independent of the solvent. In some respects our expectations are justified and find their expressions in the van’t Hoff laws; but on the other hand, we cannot fail to see that the solvent plays a very important part, for many substances refuse altogether to dissolve in certain solvents, and consequently the simplicity of the gaseous condition cannot be carried over directly to solutes without running the risk of 1 straying away from the path leading to a satis- factory explanation of solution. It was in the hope of finding that the different molecular aggregations of the solutes would explain their differences in solubility that the following experiments were made. It was in the hope of finding that in a saturated solution the osmotic pressure of the solute in the form of simple molecules would be the same in all solvents because the liquid phases are all bal- anced by the same solid phase, that is by the same undissolved solute. The large number of measurements of the solubilities of metallic salts were not available on account of ionic decomposition. The same solutes and solvents were chosen which were used in determining heats of solu- tion* and in determining molecular weights in concentrated solutions.t The apparatus shown in figure 1 was used; the tube A was about 17° long and 25™ wide; B was about 12° long and about 2°0™ wide; © was about of the same size as B. Solu- tion, excess of solute and thermometer were in A. At the bottom of B was a plug of filter paper, ); otherwise B was empty, and C wasempty. After the tubes were char ged, they were sunk in a water bath nearly to the tops of B and C. The solution and solute were kept stirred by air blown through O, the air escaping around the loosely fitting stopper of A. When * Journ. Am. Chem. Soc., xviii, 146, 1896. + This Journal, xiii, 213, 1902. 294 C. L. Speyers—Solubilities of Some Carbon the solvent was other than water, the air was dried by calcium ~ cehlorid. About half an hour was needed to get the temperature of the water bath constant to 0°1° for ten minutes. When that was done, at the end of the ten minutes, the solution with undis- solved solute was drawn over into B, and through the filter plug into ©. When the solute was a nitrogenous body, the solution was analyzed by the Kjehldahl method; by specific gravity, when the solute was non-nitrogeneous. "Evaporation to dryness and weighing the residue was altogether unsuitable, too much decomposition. The solutions were believed to be in just the right condition, since the large mass of crystals present when the solution was drawn over must have prevented appreciable supersaturation on the one hand, and on the other, as the temperature was always falling at this time, though only very slightly, the solu- tion must have been completely “saturated, The thermometer was carefully calibrated. It was divided into tenths and the temperature is probably correct to this quantity, but hardly correct to a smaller quantity on account of the uncertainty of the temperature of the exposed thread. The examination and purification of solvents and solutes have already been described.* The following tables give the results caleulated to per cent gram-molecules, that is, to the number of gram-molecules of solute in 100 gram-molecules of solution at the accompanying temperature. The usual chemical formule were used in the calculations. WATER. Chloral Urea. Urethane. hydrate. Succinimid. Acetamid. Resorcinol.: 0-07: 16°77 O:0 Bb 0°0° 20°66 0°0° 1°58 0°0° 29°64 3500 eee 11°0° 20°82 10°3°. 6°09 11°3° 30°23 11°3° 2°74 10°6°° 34°35) TO aie 19°8° 22°69 “11°1° 6°62 23°7° 45°86 20°7°° 4°23 19°9° 40°72. oe 31°7° 28°24 23°5° 43°70 38°1° 59'41 °33°3° 9:91 39°9°° 40:62) anes eee 51-40 S667 el4o soe el 69°3° 27:14 45°5° 60°14 VWoer som 69°5° 4915) 1870-075 °58 63°0°.7 740 MeETHYL ALCOHOL. Urea. Urethane. Acetanilid. Naphthalene. Acenaphthene. O°0° (eas OO". S1-18 F077 Se eacss 00" =) Ored 00% §«=0°3 9% 10°S° “Heaval 10°6° 41°70 115? E709 146°" 4-68 12-4". 0°38 21°7° 10°81 99°5° 58:58 99°38? Te 1e 31°89 210-57 30°7°: 0°Tam 404° 15°96 40°9° 90:00 33°6° 1396 AS-Oon se sae A6°0°. —-:1°5S 612°. ar ge 402 Ya 17-05 59°9° (12°34 62°3° 29-46% ATA? > “DB-79 60°9° 35:24 63°35 .83°38 * This Journal, 1. ¢. Compounds and Densities of their Solutions. 295 ETHYL ALCOHOL. Urea. Urethane. Acetanilid. Naphthalens. Resorcinol. Acenaphthene. freon 23°91 00°) 501 . 0-0". 1°80 0°0° 34:37 0°0° 0°57 3°04 10°5° 36°86 10°8° 6°84 86. Stee o-2>. 37-69 “Oe 0-84 meeeestigeas ol) 49°57 17-93 318° 489 31°8° 41°84 30°3°. 1°70 BGbs0-9- 72°35 43°5° 15°40 46°9° 9-70 50°6° 47°07 49°8° 3°86 ies S032 61°6° 31°36 69°8° 64°92 73°1° 58°03. 71°6° 12°94 _ Phenan- Chloral | _ threne. hydrate. Succininid. Acetamid. Benzamid. p-Toluidin. Os2— 0-0° 34°35 00°. Ges 900° 185305200" S06 0°0° 20°72 eee 41-08 11-1°.. 1-36 -18°6° 32°87 10°4° 4:25 11°7° 33°88 meee S316. 24°2° 2°44 49°5° 56°06 32°6° 8°72 . 22°1° 50°90 BG ASA? 92°32 43°7° 5°63 62°0° 78°92. 50°4° 14°44 ae bea 58°6° 11°49 722°. 20°86 PrRopyL ALCOHOL. Urethane. Naphthalene. Acenaphthene. 00° 19°48 0:0° 2°09 0:0° 0°88 mee. 59°97 10°4° 2°70 10°5° 0°97 91 53°31 30°3° 5°34 Sib 1°88 30°4° 68°75 50°3° 15°34 50°3° 4°37 40°7° 85°74 68°5° 62°9 Pa 4 9-8 CHLOROFORM. Chloral Urethane. Acetanilid. Naphthalene. Acenapthene. hydrate. Pee see 0) 63-24 «070° 19°58 0-0° 12°72 0:°0° 2°67 weet oe 106 7-32. 10°6°°23-714. 11°2° 16°54 12°5° 4-293 Reeeteroa abs 15°64 30°3° 38°53 29°8° 54-62? 27-7° 31-93 311° 69°92 45°9° 24:07 52°5° 57°40 52°7° 42°19 44-0° 100°0 epee test 61°4° 37°55 44°4° 100°0 46°3° 100°0 TOLUENE. Phenan- Chloral Urethane. Naphthalene. Acenaphthene. threne. hydrate. ore O 12°82 0:0°' 788 ~0-0° 11-88 0:0° 1°78 eared 25:2" 23-96 10°3° 10°76 13°9° 17°40 10°0° 4:24 S39 Ga60 46°3° 47°37 24°1° 16°53 30°8° 26°90 20°7° 11°42 4A0°7° 87°86 69°5° 84°43 41°6° 29°29 54°9° 53°25 29°6° 31°18 61°5° 45°08 78°3° 81°98 42°5° 89°86 It is unnecessary to plot these data, for with the exceptions of urethane in water and chloral hydrate in chloroform, the curves are quite regular. In the cases of urethane and chloral hydrate, the curves change direction very suddenly at about 12°, showing a very sudden decrease in solubility as the tem- perature decreases from this point. 296 C. L. Speyers—Solubilities of Some Carbon Plots showing the variation in solubility as we pass from one solvent to another are perhaps of some interest. They are GAA genie CHL, ) /0 Zo 30 Sutcinimid ee NeANE —! WEN ° S S w 8 N NN La a iA eat ea os: | Lith slene : = Hey Rie hy B 5 a pe be Ho B22 =" 10 20 30 0 50 60 70 o /0 ZO JO 7) 50 se Aulamnia Resoreinst given in figures 2 and 3. The solubilities are expressed in per- centage gram-molecules* along the horizontal line in that sol- * According to the ordinary chemical formule. Compounds and Densities of their Solutions. 297 vent whose formula is.given at the commencement of the line. We notice that the relative solubility of a solute in several solvents can change very much with the temperature. For instance, acetamid is less soluble in alcohol than in water between 0° and about 50°, but above 50° it is more solable in aleohol than in water. This is analogous to the relative changes in vapor pressures of some liquids. We notice the small increase in solubility of urethane in water as we pass from 0° to 10° and the rapid increase as we pass beyond that temperature. There seems to be some slight error in the solubility of the aqueous solution at 30°, but there is none at 10°, for the solubility at that temperature was determined twice. We notice also that there is no regularity in change of solubility as the molecular weights of the alcoholic solvents increase, whether we consider the molecular aggregations of the solutest or not. M. Schroedert has deduced the equation n ae = A(t,-t) in which 7 is the number of gram-molecules of solvent in a saturated solution; A is a constant, the same for each solute whatever the solvent may be. 7, is the fusion temperature of the solute and z is the temperature of saturation. How this equation is obtained need not be considered. According to it, the curves of solubility of any solute in all solvents should coincide. Schroeder tested the equation with p-dibrombenzene in ethyl alcohol, propyl alcohol, isobutyl alcohol, ethyl ether, earbon disulphid, benzene, and brombenzene; with naphthalene in benzene. chlorbenzene, and carbon-tetrachloride;. with m-dinitrobenzene in benzene, brombenzene, and chloroform. His results justify it, but mine do not; only for solutions of acenaphthene, naphthalene, and phenanthrene are the coinci- dences at all good. The specific volumes of the solutions must be known before we can proceed to determine the osmotic pressures of the solutes, and therefore we now pass on to the densities. These were easily obtained by sinking a pycnometer with a very small mouth into the saturated solution and drawing this in, the very small mouth keeping out particles of solute. Since the solution was kept stirred by air and contained an abundant excess of solute and since the temperature was kept constant for some ten minutes before drawing into the pyc- nometer, the solutions are to be considered in just the right + This Journal, 1. c. ¢ Zeitschr. Phys. Chemie, xi, 449, 1893. 298 C. L. Speyers—Solubilities of Some Carbon condition, neither supersaturated nor undersaturated. The thermometer was the one used for the solubilities and the tem- perature is certain to 0°1°. The uncertainty in the density is about 3 units in the third piace in extreme cases; in general it is 2 or 3 units in the fourth place, the pycnometer holding between 8°5 and 9:8" and the weighings being made to milligrams. The following tables give the temperatures and correspond- ing densities; namely, weights in grams reduced to vacuum of one cubic centimeter of solution. WATER. Chloral Urea. Urethane. hydrate. Succinimid. © BO. a~d9T 0:07 1/1028 0°02 T=438 0°0° °1°025 19-0" nei Ay 110° 12025 15:3". Tage 15°9°" "104s 39°2° 1:7158 04-0 "07s 31-0" 1578 36°6° 3 rad 463 2 ae 38°8° 1:°064 , 466° 1623 50°3° > 1s140 6475" .4°181 39-7". 2065 65°0°.) 15481 84-91%) 047196 84°4° 1°208 Acetamid. . Resorcinol. Mannitol. 0:0° 1°055 00° 108 00° ~ 1°044 15°6° 1:046 14-4? 1125 15°2°° 1050 B16) 1087 B1-1° > 449 ST? ee 49°" “1 O22? AS O° FGI 47°7° 1:099 68°4° 1°011 Go'47 ea ye 68°0° 1°148 85°4° 1°179 85°9° -1:2907 METHYL ALCOHOL. Urea. Urethane. Acetanilid. 070° 0°8612 0°0°. 0°9565 00° 0°8602 17°4° 0°8674 15°5° 0°9902 16°7° 0°8698 29°7° 0°8764 28°2° 1 oza 29°9° 0:8924 50°5° =0°9086 39°5° 1:044 43°9° 0°9206 66°8° 0°9534 61°7° 0°9596 Methyl Alcohol Naphthalene. Acenaphthene. (pure). 00° 0°8194 00° 0°8133 0°0° 08110 16°6° 0°8088 12°5> -O0B030 18°3° 0°7938 29°0° 0°8048 31:6, 0°7900 29°4° 0°7834 47°0° 0°8086 45°6° 0°7823 46°2° 0°7675 61°7° 0°8436 64°1° 0°78438 59°8° 0°7540 68°0" ,.0°9022 Compounds and Densities of their Solutions. 299 EtHyL ALCOHOL. : Chloral - Urea. Urethane. hydrate. Succinimid. Acetamid. 7 (08915 0:0° 0°8914 0°0° -£-110 0:0° 0°8150 0:0° 0°8562 Pee obs) b4°1° 0°9443. 16-7° 1319 17°5° 0°8063 17°8° 0°8696 31°6° 0°8060 30°9° 1:004 33°5° 1:°560 33°2° 0°8052. 35:0° 0°8974 aie 2 O-S0at .43°7°° 1°044 40°8° 1°589 57°5° 0°8292 54°4° 0°9416 71°5° 0°8124 79°64. 0°9552> 70:3° 0°9815 80°6° 0:9563 Resorcinol. Benzamid. Acetanilid. p-Toluidin. Naphthalene. 07 1°033 0:0° 0°83381 0-0° 0°8420 0°0° 0°8884 0°0° 0°8175 wine? O96 141° O'8328 17-2° 0°8472 15°6° 0-9168 —17:0° 0°8104 SG°h 1-054 §36-2° 0°8434 39°0° 0°8721 28°4°.0°9458 31°2° 0°8084 G29 077) 572° 078754 58°1° 0°9156 40°6° 0:9636 51°0° 0°8230 ie tr 107, 72°8° 0°9226 76°7° 0°9596 72°4° 0:9563 23 Sy sein it E Ethyl alcohol Phenanthrene. Acenaphthene. (pure). 0:0° 0°8141 0:0° 0:8108 0:0° 0°8074 15'6° 0°8035 15°0° 0°8013 - 19°1° 0°7921 35°3° 0°7960 36°3° 0°7910 35°3° 0°7780 52°2° 0°7941 53°4° 0°7890 --52:3° 0°7633 76°4° 0°8654 73°0° 0°8186 - 72°8° 0°7448 PRoPpYL ALCOHOL. Propyl alcohol Urethane. Naphthalene. Acenaphthene. (pure). “QV? ° “—H)2 . 5 “Hj? , te) , : ics nase: isp 0.8111 .« 18 0° 0.8007 29°1° 09804 30°7° 0°8206 26°6° 0°8110 28°0° 0°7991:- fet 0353 41°8° 0°8247 47°4° 0°8063 44°4° 0-7854 59°7° 0°8634 64*7— -0°8217 65°1° 0°7678 FAS 0-958 -< >8as3 - Or071sGy .S0-G° .0-7538 CHLOROFORM. | Chloral Urethane. hydrate. Acetanilid. p-Toluidin. “Me 7 Yate 1°52 “He “no Or a es 2s care 00 es aE2° £IES1 34°4° 1°565 SAD? L381 31°4° 1:066 43°4° 1°097 - 44°6° 1°615 AT:3° 1-326 40°8° 0°9906 62°47 1-261 69:9° 1:227 Chloroform Naphthalene. Acenaphthene. (pure). 0°0° 1:393 0°0° 1°438 00° 1°526 90°25 "E304 16°5° 1°378 18°2° 1°492 S52 e250 29°1° 1:°328 33°4° 1°464 53°2°) 1°E36 40°3° 1°28) 44°6° 4448 64°5° 1°072 55°8° 1:209 58-60. bab 7 300 C. L. Speyers—Solubilities of Some Carbon TOLUENE. Chloral Urethane. hydrate. p-Toluidin. Naphthalene. 0°0° 0°8872 0:0° 0:8978 0°0° 0:9110 0:0° 0°9124 18°4° 0°8792 18°5° 0°9328 16°6°, 0°9228 | 173° aSise 34°0° 0°9570 28°4° 1:069 29°4° 0°9430 36°2° 0°9224 45°2° 1:042 40°8° 1°448 40°7° 0°9616 51%") 0:93 74 42°0° 1°445 73°9° 0°9692 Phenanthrene. Acenaphthene. Toluene (pure). 0:0° 0°9254 0:0° 0:9066 0°0° 0°8840 18°3° 0°9337 13°3° 0:9076 17°6° 0°8678 37°9° 0°9515 32°3° 0°9196 32°1° 0°8544 60°1° 0°9890 57°2° 0°9502 49°8° 0°8381 86°3° 1:038 83°5° 1:006 65°9° 0°8232 85°0° 0°8048 Of these solutions, so far as they could be examined, only the following contain solutes with normal molecular weights.* Urea in water at 32° to 41° a “methyl aleohol “ 28° ““c cc ethyl “ “c a7S Acetanilid + ‘methyl > * © 31°(?) = «ethyl Fé “21 toes Naphthalene ee att 3 6 98° 6 # “«" toluene “.* ‘99°. “Aa Acenaphthene “ propylalcohol “ 45°(?) 4 *« “ toluene © 91" 10a Selecting 27° as the temperature and taking solubilities at that temperature from solubility curves and densities from density curves, we get the following table: | Osmotic Solution. Solubility. Density. Pressure. Urea in water "222s. 22222 26 grmmols 1155 10:4 atmos. “ _-gmethyl alcohol 22 - 12 i 0°873 3 Oe « ethyl eaeerare 5 ae 0805 «og Acetanilid-in methyl alcohol 12° “ 0°891 Dae ee «“ ethyl ec 14400 0°858) > a-qe eee Naphthalene inethyl alcohol 4 “ 0°810 Ota ° “ toldaene -_-- - 25 “4 0-918 a Acenaphthenein propylalcoh’] 1 ‘ 0'810 Che sd tolavene —_.. = 18 oF 0-918 Le The osmotic pressure is not at all constant for each solute, and we see that the undissolved solute does not balance the dissolved solute to an equal extent in each solvent though the molecular weights of the solutes are simple. So the analogy of solution to vaporization is seen to be far from complete. * This Journal, 1. c. Compounds and Densities of their Solutions. 301 In conclusion a few words ahout the densities and molecular volumes. There is no need of putting the data given above into plots. There is no peculiarity in any of them, not even in the aqueous solution of urethane nor in the chloroform solution of chloral hydrate, but the plets showing variation in molecular volume as a solute passes from one solvent into another are instructive. They are given in figure 4. AoW IN| CHOH Rik The formula at the beginning of the horizontal line gives the solvent, and the numbers along the horizontal give the relative volumes of one gram-molecule of solute at the temper- ature stated on the lines. For example, the relative volume of one gram-molecule of acenaphthene in chloroform at 10° has been obtained in this way :— Solubility of acenaphthene from solubility curve=16°0% gram- mols. . Proportion of chloroform=84°0*119°3/ (84°0° 1193 + 16°0° 154). Volume of one gram chloroform at 10° from density curve= 1/1°51ce. «© chloroform in one gram of solution is [84°0*119:3/ (84:0 *119°3 +16°0* 154)] 1/1°51cec=0°5327ce. « one gram of solution at 10°=1/1°40ce. « © acenaphthene in one gram of solution=1/1°40—0°5327 =0°1811ce. «< _ corresponding to one molecule of acenaphthene=0°1811/16 =0°'0113. Am. Jour. Sc1.—FourtH SERIES, Vout. XIV, No. 82.—OcToBsr, 1902. 21 302 Speyers—Solubilities of Some Carbon Compounds, ete. For convenience, the values are all multiplied by 1000 before plotting. We notice the following :— The molecular volumes of the solutes are larger in water than in the other solvents and decrease in the order of methyl alcohol, ethyl alcohol, propyl! alcohol, toluene and chloroform, the only exception being perhaps choral hydrate in ethyl alcohol compared to its solution in chloroform. The molecular volumes in chloroform show decided constancy for every temperature and concentration observed, and to a lesser extent in toluene. : In general, the molecular volumes of the solutes decrease as the temperature rises and the concentration increases. The exceptions are urethane and chloral hydrate in chloroform. Rutgers College, April, 1897-June, 1902, Chemistry and Physics. 303 SGLtENTIFIC INTELEIGENCE. I. CHEMISTRY AND PHysIcs. 1. Radio-active Bismuth.—Polonium, the radio-active sub- stance occurring with bismath in pitchblende, was the first of these substances discovered (by Mr. and Mrs. Curie). Subse- quent investigations by Giesel led the latter to believe that polonium was nothing more than bismuth made active by induc- tion. Marck wa p, however, has recently obtained results which indicate that polonium is a distinct element. From a by-product obtained from pitchblende, by the usual methods, bismuth oxy- chloride was prepared which was strongly radio-active, and which showed no decrease in activity after several months. Upon subjecting a solution of this substance to electrolysis, it was found that the metal which was deposited at first displayed much greater activity than the final product. This result led to the attempt to precipitate polonium, from hydrochloric acid solu- tions of the oxychloride, by means of a polished stick of metallic bismuth. As a result, the metal became coated immediately with a fine black deposit, which gradually increased, and when it had been removed from the solution and washed, it showed a surpris- ingly strong effect on the electroscope. At the distance of a decimeter the leaves of the charged electroscope collapsed in a moment, and even a gutta-percha rod which had been well rubbed with fur was immediately discharged upon the approach of the bismuth stick. The important fact was noticed that metallic bismuth is thus able to remove practically all of the active material from a solution. The powder could be scraped from the bismuth rod, and the amount thus obtained from 8§ of bis- muth oxychloride was about 5™%. From this result it was calcu- lated that a ton of pitchblende would contain not more than one gram of the substance. The powder was found not to be a pure metal, but to contain some chlorine. Upon heating, a small por- tion volatilized, probably as chloride, and the residue fused to a white, exceedingly brittle, metallic bead. This was soluble in nitric acid, and the solution, as far as it could be tested, gave reactions for bismuth. The salts are as strongly active as the metal, and the rays are characteristically different from those of radium in being unable to penetrate any intervening substance. Even a piece of filter-paper wrapped around a stick of bismuth coated with the active metal causes it to lose all its effect. The experiments are to be continued with larger quantities of material, and it is hoped that an atomic weight determination may be made.— Berichte, xxxv, 365. . H. L. W. 2. A Thermochemical Constant.—F. W. CLARKE, in a pre- liminary paper, has made a generalization from a consideration of Thomsen’s work on the heats of combustion of certain organic compounds. In the first place, he has re-caleulated Thomsen’s 304 Scientific Intelligence. results so that they represent the formation of gaseous instead of liquid water. He then finds for the aliphatic hydrocarbons and their non-oxygenated derivatives that ___ +4 ee 12a+6b—c—8n stant, where A represents the heat of combustion of the com- pound, @ the number of molecules of CO, produced, 6 the num- ber of molecules of H,O, ¢ the number of oxygen molecules involved, and 2 the number of atomic unions or linkings in the compound burned. In fixing the value of n, double and triple linkings are not distinguished from simple ones, so that for all chain molecules m is equivalent to the number of atoms minus one. The coefficients 4, 12, 6, | and 8 appear to have been chosen arbitrarily, but the results obtained with them in the cases of fourteen hydrocarbons are remarkably uniform, and the author evidently considers it important that the constant, which averages 13,878 in this case, is very near the neutralization con- stant of acids and bases, which is 13,700 calories. The same uniform constant was obtained with many other organic com- pounds by modifying the formula in accordance with the presence of several other elements : thus for halogen compounds were used 4K 4k and 124+6b+h—c—8n 12a4-664+2h,—ce—8n the formulas 41 12a+6b+4h,—ce—8n’ of chlorine, bromine and iodine molecules, supposed by the author to be formed by the complete combustion of the halides. For nitrogen compounds two formulas were used ; for cyanides and nitrites, where m represents the number of nitrogen molecules set free, the divisor is 124+6)6+3m—c—8m, while for amines 3m is replaced by 9m. For sulphur compounds the term 9s is intro- duced, while c,, the number of oxygen molecules present in the compound, is subtracted when the latter element is present. In this way conformable results were obtained with nineteen halogen compounds, four cyanides, ten amines, eight sulphur compounds, and eleven alcohols. The ring compounds have not yet been worked out in this way, and there are a few substances in most of the groups which fail to give the usual result. A considera- tion of the exceptions is deferred until the complete memoir is published. The conclusion is reached that, in any class of com- pounds, the heat of formation is proportional to the number of atomic linkings within the molecule, and seems to bear no rela- tion to the masses of the atoms which are combined. It is to be hoped that Professor Clarke has discovered a new and important thermochemical law, but from the arbitrary nature of the formulas used the suspicion arises that the law may be a very obscure one.—Jour. Amer. Chem. Soc., xxiv, 882. H.L. W. 3. The Heatless Condition of Matter.—In the June number of this Journal mention was made of Brinkworts and MarrTin’s theory that pressure may be able to prevent moleeular vibration where h, h, and h, represent the numbers . Chemistry and Physics. 305 and thus cause matter to assume a condition which is devoid of heat. In regard to that notice the editor has received from one of the authors a letter which is too long to be inserted, but which should be acknowledged here. It does not appear that objection is made to our presentation of the main points of the theory, but in relation to our opening remark, “ Brinkworth and Martin, with apparent seriousness, have made a curious extension of the kinetic theory,” the letter says, “ Your abstractor appeared to doubt the seriousness of the paper. I write at once to say that in this matter we are in deadly earnest.” The fact is, we intended to convey the idea that the seriousness of the article impressed us. Objection is made to our opinion that “Their deductions are based upon an entirely unproven assumption,” and, in this connection, the letter refers to some points which are to be brought out in a future article. It seems to us that no injustice has been done to the authors as far as their preliminary publication is concerned, and that further discussion of their theory should be postponed until their more elaborate paper has appeared. H. Ti. W. 4. Elementary Chemistry, by F. W. Criarke and L. M._— Dennis. 12mo. Pp. 340. New York, 190% (American Book Company).—In preparing this little text-book the authors have aimed especially to make it a means of training in the interpreta- tion of evidence. Each generalization is made to follow the evidence upon which it rests. The work is accompanied by a laboratory manual, but a reasonable number of experiments, nearly all of which are of the simplest character, are described throughout the text. The book appears less dry and more inter- esting than most of the works on the subject on account of the constant attention which is paid to the application of chemistry to human affairs and its utility in modern life. The authors have done no more with the theory of ionization than to give it a very brief mention. Although they consider this theory unsuitable for discussion in a work of this kind, it seems probable that its use In a simple manner would present no more difficulty to the beginner than some of the theories which are introduced. It is satisfactory to notice that the book contains a short treatise (about 60 pages) on organic chemistry, a subject which is too often omitted in books on elementary chemistry. Very few things have been noticed in the work which seem unsatisfactory, but it appears that the somewhat imaginary structural formula for the double sulphate of magnesium and potassium (p. 202) is hardly appropriate in such a book, and objection may be made to the equation KCIO,=KC1+0,, because O, is ozone. A mistake is made in characterizing lithium as the lightest solid known, for solid hydrogen is mentioned in the book. H..L.. We 5. Liquid Hydrogen and Helium; from the inaugural address delivered at Belfast by Prof. James Dewar, President of the Brit- ish Association.— * * * From this speculative divergency it is clear no definite conclusion could be reached regarding the physical prop- 306 Scientific Intelligence. erties of liquid or solid hydrogen, and the only way to arrive at the truth was to prosecute low-temperature research until success attended the efforts to produce its liquefaction. This result I definitely obtained in 1898. The case of liquid hydrogen is, in fact, an excellent illustration of the truth already referred to, that no theoretical forecast, however apparently justified by analogy, can be finally accepted as true until confirmed by actual experiment. Liquid hydrogen is a colorless, transparent body of extraordinary intrinsic interest. It has a clearly defined surface, is easily seen, drops well, in spite of the fact that its surface tension is only the thirty-fifth part of that of water or about one-fifth that of liquid air, and can be poured easily from vessel to vessel. The liquid does not conduct electricity, and, if anything, is slightly diamagnetic. Compared with an equal volume of liquid air, it requires only one-fifth the quantity of heat for vaporization; on the other hand, its specific heat is ten times that of liquid air or five times that of water. The coefficient of expansion of the fluid is remarkable, being about ten times that of gas; it is by far the hghtest liquid known to exist, its density being only one- fourteenth that of water; the lightest liquid previously known was liguid marsh gas, which is six times heavier. The only solid which has so small density as to float upon its surface is a piece of pith wood. Itis by far the coldest liquid known. At ordi- nary atmospheric pressure it boils at minus 252°5 degrees or 20°5 degrees absolute. The critical point of the liquid is about 29 degrees absolute and the critical pressure not more than fifteen atmospheres. ‘The vapor of the hydrogen arising from the liquid has nearly the density of air—that is, it is fourteen times that of the gas at the ordinary temperature. Reduction of the pressure by an air-pump brings down the temperature to minus 258 degrees, when the liquid becomes a solid resembling frozen foam, and this by further exhaustion is cooled to minus 260 degrees, or 13 degrees absolute, which is the lowest steady temperature that has been reached. The solid may also be got in the form of a clear, transparent ice, melting at about 15 degrees absolute, under a pressure of 55™™, possessing the unique density of one- eleventh that of water. Such cold involves the solidification of every gaseous substance but one that is at present definitely known to the chemist, and so liquid hydrogen introduces the investigator to a world of solid bodies. The contrast between this refrigerating substance and liquid air is most remarkable, On the removal of the loose plug of cotton-wool used to cover the mouth of the vacuum vessel in which it is stored, the action is followed by a miniature snow-storm of solid air, formed by the freezing of the atmosphere at the point where it comes into con- tact with the cold vapor rising from the liquid. This solid air falls into the vessel and accumulates as a white snow at the bot- tom of the liquid hydrogen. When the outside of an ordinary test-tube is cooled by immersion in the liquid, it is soon observed to fill up with solid air, and if the tube be now lifted out a Chemistry and Physics. 307 double effect is visible, for liquid air is produced both in the inside and on the outside of the tube—in the one case by the melting of the solid, and in the other by condensation from the atmosphere. A tuft of cotton-wool soaked in the liquid and then held near the pole of a strong magnet is attracted, and it might be inferred therefrom that liquid hydrogen is a magnetic body. This, however, is not the case: the attraction is due neither to the cotton-wool nor to the hydrogen—which indeed evaporates almost as soon as the tuft is taken out of the liquid—but to the oxygen of the air, which is well known to be a magnetic body, frozen in the wool by the extreme cold. The strong condensing powers of liquid hydrogen afford a simple means of producing vacua of very high tenuity. When one end of a sealed tube containing ordinary air is placed for a short time in the liquid, the contained air accumulates as a solid at the bottom, while the higher part is almost entirely deprived of particles of gas. So perfect is the vacuum thus formed, that the electric discharge can be made to pass only with the greatest difficulty. Another important application of liquid air, liquid hydrogen, etc., is as analytic agents. Thus, if a gaseous mixture _ be cooled by means of liquid oxygen, only those constituents will be left in the gaseous state which are less condensable than oxygen. Similarly, if this gaseous residue be in its turn cooled in liquid hydrogen, a still further separation will be effected, everything that is less volatile than hydrogen being condensed to a liquid or solid. By proceeding in this fashion it has been found possible to isolate helium from a mixture in which it is present to the extent of only one part in one thousand. By the evaporation of solid hydrogen under the air-pump we can reach within 13 or 14 degrees of the zero, but there or thereabouts our progress is barred. This gap of 13 degrees might seem at first insignificant in comparison with the hundreds that have already been conquered. But to win one degree low down the scale is quite a different matter from doing so at higher temperatures; in fact, to annihilate these few remaining degrees would be a far greater achievement than any so far. accomplished in low- temperature research. For the difficulty is twofold, having to do partly with process and partly with material. The application of the methods used in the liquefaction of gases becomes con- tinually harder and more troublesome as the working tempera- ture is reduced ; thus, to pass from liquid air to liquid hydrogen —a difference of 60 degrees—is, from a thermodynamic point of view, as difficult as to bridge the gap of 150 degrees that sepa- rates liquid chlorine and liquid air. By the use of a new liquid gas exceeding hydrogen in volatility to the same extent as hydrogen does nitrogen, the investigator might get to within five degrees of the zero; but even a second hypothetical sub- Stance, again exceeding the first one in volatility to an equal extent, would not suffice to bring him quite to the point of his ambition. That the zero will ever be reached by man is 308 Scientific Intelligence. extremely improbable. A thermometer introduced into regions outside the uttermost confines of the earth’s atmosphere might approach the absolute zero, provided that its parts were highly transparent to all kinds of radiation, otherwise it would be affected by the radiation of the sun, and would therefore become heated. But supposing all difficulties to be overcome, and the experimenter to be able to reach within a few degrees of the zero, it is by no means certain that he would find the near approach of the death of matter sometimes pictured. Any fore- cast of the phenomena that would be seen must be based on the assumption that there is continuity between the processes studied at attainable temperatures and those which take place at still lower ones. Is such an assumption justified? It is true that many changes in the properties of substances have been found to vary steadily with the degree of cold to which they are exposed. But it would be rash to take for granted that the changes which have been traced in explored regions continue to the same extent and in the same direction in those which are as yet unexplored. Of such a breakdown low-temperature research has already yielded a direct proof at least in one case. A series of experiments with pure metals showed that their electrical resistance gradually decreases as they are cooled to lower and lower temperatures, in such ratio that it appeared probable that at the zero of absolute temperature they would have no resistance at all and would become perfect conductors of electricity. This was the inference that seemed justifiable by observations taken at depths of cold which can be obtained by means of liquid air and less powerful refrigerants. But with the advent of the more powerful refrig- erant liquid hydrogen it became necessary to revise that conclu- sion. A discrepancy was first observed when a platinum resistance thermometer was used to ascertain the temperature of that liquid boiling under atmospheric and reduced pressure. All known liquids, when forced to evaporate quickly by being placed in the exhausted receiver of an air-pump, undergo a reduction in tem- perature, but when hydrogen was treated in this way it appeared to be an exception. The resistance thermometer showed no reduc- tion as was expected, and it became a question whether it was the hydrogen or the thermometer that was behaving abnormally. . Ultimately, by the adoption of other thermometrical appli- ances, the temperature of the hydrogen was proved to be lowered by exhaustion as theory indicated. Hence it was the platinum thermometer which had broken down ; in other words, the elec- trical resistance of the metal employed in its construction was not, at temperatures about minus 250° C., decreased by cold in the same proportion as at temperatures about minus 200°. This being the case, there is no longer any reason to suppose that at the absolute zero platinum would become a perfect conductor of electricity ; and in view of the similarity between the behavior of platinum and that of other pure metals in respect of tempera- ture and conductivity, the presumption is that the same is true of Chemistry and Physics. 309 them also. At any rate, the knowledge that in the case of at least one property of matter we have succeeded in attaining a depth of cold sufficient to bring about unexpected change in the law express- ing the variation of that property with temperature, is sufficient to show the necessity for extreme caution in extending our infer- ences regarding the properties of matter near the zero of tempera- ture. Lord Kelvin evidently anticipates the possibility of more remarkable electrical properties being met with in the metals near the zero. A theoretical investigation on the relation of “elec- trions” and atoms has led him to suggest a hypothetical metal having the following remarkable properties: below 1 degree absolute it is a perfect insulator of electricity, at 2 degrees it shows noticeable conductivity, and at 6 degrees it possesses high conductivity. It may safely be predicted that liquid hydrogen will be the means by which many obscure problems of physics and chemistry will ultimately be solved, so that the liquefaction of the last of the old permanent gases is as pregnant now with future consequences of great scientific moment as was the lique- faction of chlorine in the early years of the last century. The next step towards the absolute zero is to find another gas more volatile than hydrogen, and that we possess in the gas occurring in cleveite, identitied by Ramsay as helium, a gas which is widely distributed, like hydrogen, in the sun, stars and nebule. A specimen of this gas was subjected by Olszewski to liquid air temperatures, combined with compression and subsequent expan- sion, following the Cailletet method, and resulted in his being unable to discover any appearance of liquefaction, even in the form of mist. His experiments led him to infer that the boiling- point of the substance is probably below 9 degrees absolute. After Lord Rayleigh had found a new source of helium in the gases which are derived from the Bath springs, and liquid hydro- gen became available as a cooling agent, a specimen of helium cooled in liquid hydrogen showed the formation of fluid, but this turned out to be owing to the presence of an unknown admixture of other gases. Asa matter of fact, a year before the date ot this experiment I had recorded indications of the presence of unknown gases in the spectrum of helium derived from this source. When subsequently such condensable constituents were removed, the purified helium showed no signs of liquefaction, even when compressed to 80 atmospheres, while the tube contain- ing it was surrounded with solid hydrogen. Further, on suddenly expanding, no instantaneous mist appeared. Thus helium was definitely proved to be a much more volatile substance than hydrogen in either the liquid or solid condition. The inference to be drawn from the adiabatic expansion effected under the circumstances is that helium must have touched a temperature of from 9 to 10 degrees for a short time without showing any signs of liquefaction, and consequently that the critical point must be still lower. This would force us to anticipate that the boiling- point of the liquid will be about 5 degrees absolute, or liquid 310 | Scientific Intelligence. helium will be four times more volatile than liquid hydrogen, just as liquid hydrogen is four times more volatile than liquid air. Although the liquefaction of the gas is a problem for the future, this does not prevent us from safely anticipating some of ‘the properties of the fluid body. It would be twice as dense as liquid hydrogen, with a critical pressure of only 4 or 5 atmos- pheres. The liquid would possess a very feeble surface-tension, and its compressibility and expansibility would be about four times that of liquid hydrogen, while the heat required to vaporize the molecule would be about one-fourth that of liquid hydrogen. Heating the liquid 1 degree above its boiling-point would raise the pressure 1# atmospheres, which is more than four times the increment for liquid hydrogen. The liquid would be only seven- teen times denser than its vapor, whereas liquid hydrogen is sixty- five times denser than the gas it gives off. Only some 3 or 4 degrees would separate the critical temperature from the boiling- point and the melting-point, whereas in liquid hydrogen the sepa- ration is respectively 10 and 15 degrees. As the liquid refractivi- ties for oxygen, nitrogen and hydrogen are closely proportional to the gaseous values, and as Lord Rayleigh has shown that helium has only one-fourth the refractivity of hydrogen, although it is twice as dense, we must infer that the refractivity of liquid helium would also be about one-fourth that of liquid hydrogen. Now hydrogen has the smallest refractivity of any known liquid, and yet liquid helium will have only about one-fourth of this value—comparabie, in fact, with liquid hydrogen just below its critical point. This means that the liquid will be quite excep- tional in its optical properties, and very difficult to see. This may be the explanation of why no mist has been seen on its adia- batic expansion from the lowest temperatures. Taking all these remarkable properties of the liquid into consideration, one is afraid to predict that we are at present able to cope with the difficulties involved in its production and collection. Provided the critical point is, however, not below 8 degrees absolute, then from the knowledge of the conditions that are successful in pro- ducing a change of state in hydrogen through the use of liquid air, we may safely predict that helium can be liquefied by follow- ing similar methods. If, however, the critical point is as low as 6 degrees absolute, then it would be almost hopeless to anticipate success by adopting the process that works so well with hydrogen. The present anticipation is that the gas will succumb after being subjected to this process, only, instead of liquid air under exhaus- tion being used as the primary cooling agent, liquid hydrogen evaporating under similar circumstances must be employed. In this case, the resulting liquid would require to be collected in a vacuum vessel the outer walls of which are immersed in liquid hydrogen. The practical difficulties and the cost of the operation will be very great; but, on the other hand, the descent to a temperature within 5 degrees of the zero would open out new vistas of scientific inquiry, which would add immensely to our Chemistry and Physics. 311 knowledge of the properties of matter. To command in our laboratories a temperature which would be equivalent to that which a comet might reach at an infinite distance from the sun would indeed be a great triumph for science. If the present Royal Institution attack on helium should fail. then we must ultimately succeed by adopting a process based on the mechanical production of cold through the performance of external work. When a turbine can be worked by compressed helium, the whole of the mechanism and circuits being kept surrounded with liquid hydrogen, then we need hardly doubt that the liquefaction will be effected. In all probability gases other than helium will be discovered of greater volatility than hydrogen. It was at the British Association Meeting in 1896 that I made the first sug- gestion of the probable existence of an unknown element which would be found to fill up the gap between argon and helium, and this anticipation was soon taken up by others and ultimately con- firmed. Later, in the Bakerian Lecture for 1901, I was led to infer that another member of the helium group might exist having the atomic weight about 2, and this would give us a gas still more volatile, with which the absolute zero might be still more nearly approached. It is to be hoped that some such element or elements may yet be isolated and identified as coronium or nebulium. If amongst the unknown gases possessing a very low critical point some have a high critical pressure instead of a low one, which ordinary experience would lead us to anticipate, then such diffi- cultly liquefiable gases would produce fluids having different phys- ical properties from any of those with which we are acquainted. Again, gases may exist having smaller atomic weights and densi- ties than hydrogen, yet all such gases must, according to our present views of the gaseous state, be capable of liquefaction before the zero of temperature is reached. ‘The chemists of the future will find ample scope for investigation within the appar- ently limited range of temperature which separates solid hydrogen from the zero. Indeed, great as is the sentimental interest attached to the liquefaction of these refractory gases, the import- ance of the achievement lies rather in the fact that it opens out new fields of research and enormously widens the horizon of physical science, enabling the natural philosopher to study the properties and behavior of matter under entirely novel conditions. This department of inquiry is as yet only in its infancy, but speedy and extensive developments may be looked for, since within recent years several special cryogenic laborator! ies have been established for the prosecution of such researches, and a liquid-air plant is becoming a common adjunct to the equipment of the ordinary laboratory.— Nature, Sept. 11, 1902. 6. Vapor-pressures of Liquid Oxygen and of Liguid Hydro- gen.—In an abstract of a paper by M. W. Travers, G. SENTER and A. JAQuEROD read before the Royal Society on June 19 (Nature, vol. lxvi, p. 382), the results contained in the following table are given : 312 Scientific Intelligence. Vapor Pressures. LIQUID OXYGEN. Liquip HyDROGEN. Pressure Temp. on Temp. on Temp. on Temp. on inmm. hydrogen scale. helium scale. hydrogen scale. helium scale. fe) fo) le) (e} 800 90°60 90°70 20°41 20°60 760 90°10 90°20 20°22 20°41 700 89°33 89°43 19°93 20°12 600 87°91 88°01 19°41 O56: 500 86°29 86°39 18°82 19°03 400 84°39 84°49 LS ks 18°35 300 82°09 BZ k8 17°36 Lad 200 ROZO7 G17 16°37 16°57 100 fs Bele 14°93 15°13 50 ee OF oes She 14°11 The authors add, in conclusion : “Though the pressure coefficients of hydrogen and helium between 0° and 100° C. show no appreciable difference, measure- ments of low temperatures on the scales of the two thermometers are not identical. It is probable that at the normal temperature both gases may be considered as so nearly perfect that the differ- ence between the gas scale and the absolute scale is insignificant. As the critical point of helium les much lower than that of hydrogen, measurements of low temperatures on the helium scale should approach more closely to absolute temperatures than mea- surements on the hydrogen scale. It is pointed out that helium should replace hydrogen as the normal thermometric substance. The melting point of hydrogen was found to be 14°'10 on the helium scale. The pure helium used in the thermometric measurements was obtained by passing purified cleveite gas through a coil cooled to 15° in liquid hydrogen boiling iz vacuo. An unsuccessful attempt was made to liquefy this gas, which could not be con- densed at 13° under a pressure of 60 atmospheres. The vapor pressures of solid neon were measured at tempera- tures corresponding to 20°:4 (12°8™™) and 15°°65 (2°4™™). It was shown that the vapor pressure did not change as the solid evapo- rated, proving that neon is a homogeneous substance.” Il. GEoLogcgy AND MINERALOGY. 1. Martinique-—The July issue of the National Geographic Magazine is called the ‘‘ Martinique number,” and is devoted to descriptions and discussions of the volcanic eruption of Mt. Pelée which began in May last, together with some references to the contemporaneous eruption of La Soufriére on the island of St. Vincent. The number is of double the usual size and is a valua- ble contribution to the study of the recent eruptions in the Lesser Antilles, containing as it does the reports of Robert T. Hill, of the United States Geological Survey, and Israel C. Russell, of the University of Michigan, two of the representa- Geology and Mineralogy. 3813 tives commissioned by the National Geographic Society to inves- tigate the phenomena attending the cataclysms. The number is enriched by the notes by J. S. Diller on the volcanic rocks collected by Hill and Russell; by a chemical discussion by W. F. Hille- brand of analyses of ejecta from the two islands, and by a com- pilation by James Page of the reports of vessels as to the area over which the dust from the eruptions was distributed. The number is well illustrated with four maps and nineteen photographs. Four- teen of the latter are from excellent negatives taken by Russell. Hill’s report opens with a brief general statement of the geog- raphy and geology of the whole chain of the Windward Islands or Lesser Antilles, which are almost entirely volcanic in charac- ter, with the exception of Barbados. He holds that the volcanoes of these islands date back to Eocene time, at least; that the greater masses of the present volcanic heights were piled up before the Pliocene, and that “the present craters are merely secondary and expiring phenomena.” In discussing the present eruption, after relating the premonitory events of the preceding fortnight, Hill gives in detail the history of the great outburst of May 8 as derived from the accounts of eyewitnesses, and then elaborates his personal observations, which were made between May 21 and 30. He holds that the eruption which destroyed St. Pierre came from a crater low down on the southwest slope of Mt. Pelée, two miles from the northern limit of the city and a mile and a half from the sea, which he calls the “Soufriére” or “ tang Sec” crater. He considers the mud-flows to be primary phenomena of the eruption and to have come from this crater and from several “ mud-craters” on the slopes of the mountain, the sites of some of which had long been known as thermal springs. Hill calculates that only 12°5 square miles, or one-twentieth of the total area of Martinique, have been seriously affected by the eruption. No great geological changes have been brought about, but the configuration of the summit and the outline of the sea- coast have been changed somewhat. He says, ‘‘ There have been no lava flows whatsoever... . No true bombs have been ejected or molten rock in any form.” His conclusion is that conflagra- tion and death in St. Pierre may ultimately be explained by either of two theories : (1.) The heat-blast theory. This hypothesis assumes that the lapilli, gases, and steam of the ejected cloud were sufficiently hot to have inflamed the city and destroyed the people by singeing, suffocation, and asphyxiation. It does not account for the forces exerted radially and horizontally, nor for the flame. (2.) The aérial-explosion theory. The explosion of gases within the erupted cloud after their projection into the air would account for all the phenomena observed. Russell’s report takes the form of a letter to the Society. He does not subscribe to the opinion that the inhabitants of St. Pierre were asphyxiated by noxious gases or killed by a gas explosion. 314 Scientific Intelligence. He holds that the general cause of death and destruction was a blast of steam charged with hot dust, which passed through the city with hurricane force, and that gases, probably in part inflam- mable, were present, but played only a secondary part in the dis- aster. Most of Russell’s report is devoted to St. Vincent. He holds that the destruction on this island was due to dust, lapilli and stones which fell on the land while yet hot ; but that a hurricane blast of steam charged with burning dust did not sweep down from La Soufriére as it did from Mt. Pelée. Thearea of devasta- tion on St. Vincent was much greater than on Martinique. Atten- tion is called to the violent secondary or superficial eruptions due to rain or river water coming into contact with the still heated interior of the great deposits of recent ash in the gorges of the Wallibou and Dry Rivers; to the pulsating flow of the Wallibou river due to overloading by voleanic sand; to the canyon-like dendritic drainage forms already produced in the coating of fresh dust and lapilli by the rains ; and to the fact that houses standing on the windward (east) slope of the volcano had suffered most on the sides farthest from the crater. : Five miles from the crater Russell found the level fields coated with a layer of new volcanic débris about two feet thick. This would be a minimum measure and the average thickness of the deposit would be several times as great. The greater part of the débris consists of gray scoriaceous andesite and came from the columns of fresh lava that rose in the conduit of La Soufriére, This material was sufficiently cooled to become solid before it was blown into the air, and to a great extent was reduced to dust by the sudden expansion of the steam it contained. In addition to the fragments of fresh lava the fields were strewn with angular masses of older and much more compact lavas torn from the throat of the volcano. Diller describes the older lavas of Martinique, collected by Hill, as being hypersthene andesite, hornblende-hypersthene ande- site, hornblende andesite and dacite (quartz andesite), and the products of the May eruption of Mt. Pelée as belonging to the hypersthene-andesite class. He says that the specimens from St. Vincent are of hypersthene andesites, remarkable for their con- tent of olivine. Hillebrand concludes that, while the ejecta from the two vol- canoes are of the same general type, and while the material from the same vent may vary in composition within limits, according as it is collected near to or far from the vent, and in coherent or finely divided form, yet there are characteristic differences by which it appears easy to distinguish the product of one volcano from that of the other. Diller’s report is accompanied by seven analyses of pumice, sand and dust from these eruptions and Hillebrand’s discussion by three such analyses. E. O. H. 2. The Report of the Geological Survey of Louisiana: G. D. Harris, A. C. Veatcu, J. Pacneco.—The papers contained in Geology and Mineralogy. 315 this report are of especial economic value to this and neighbor- ing States, including as they do reports on the “Salines of North Louisiana,” A. C. Veatch, ‘Subterranean Waters of Louisiana ” and ‘Oil in Louisiana,” by G. D. Harris. The map of the Mississippi Embayment shows the Jackson Stage for the first time with its most probable northern distribu- tion. The statement with regard to the close of the Cretaceous is of interest at this time because of its importance to the oil industry: “In Louisiana we have reason to believe that the rais- ing and depression of the Cretaceous beds was of a much more violent nature [than farther north], that folds and faults were numerous and on a large scale and a great irregularity of surface feature characterized the newly formed rocks.” Professor Harris differs from R. T. Hill and others who believe that there are no “structural complications” in this formation. Doubt is thrown on the usually accepted theory concerning the origin of the “Mud Lumps” of the Mississippi. No new theory is advanced, but the statement is made that, “that they rise in domes or anticlines and preserve their regular bedding is proven by their structure.” “So far as we observed, none were formed as volcano-like cones.” The report on the Salines of North Louisiana, A. C. Veatch, contains:a history of the early operations of the various salt wells and licks together with well sections and a discussion of the geology. It is shown that “the principal brine springs are to be regarded as Cretaceous outcrops.” ‘The dome structure of these and other north Louisiana Cretaceous outcrops is accepted. The maps of this report and of Reports III and IV are excellent. The Reports on the Geography and Geology of the Sabine and Ouachita Rivers contain discussions and explanations of the ‘“‘Jandslip islands” of the Ouachita River and the shoals of the Sabine River which are of especial interest to physiographers. One of the most valuable reports, economically, is that on the Subterranean Waters of Louisiana. It is to be regretted that a volume containing so much valuable matter and so well illustrated by maps and half-tones is not printed on better paper and bound more substantially. 3. Die Alpen im Hiszeitalter ; von ALBrecut PrENcK und Epuarp Brickner. Parts 1 and 2. 224 pp., with many charts and figures. Leipzig. (Tauchnitz.)\—After fourteen years of investigation Professors Penck and Briickner have begun the publication of their views regarding glaciation in the Alps. The completed work will consist of about six parts, dealing with the entire Alpine system throughout the Pleistocene with especial reference to the topography resulting from ice action. In the two parts already issued Professor Penck discusses the general character of glaciers and of glacial deposits, and explains with great detail the glacial phenomena of the northern and eastern Alpine border region, particularly the area between the Iller and the Lech. 316 Scientific Intelligence. 4. Bacubirito, the Great Meteorite of Sinaloa, Mexico.—An interesting account is given in vol. iv (pp. 67-74) of the Proceed- ings of the Rochester Academy of Science, by Henry A. Warp, of a visit to the gigantic mass of meteoric iron discovered in 1876 in the State of Sinaloa, Mexico. This is perhaps the largest of all known meteorites ; its weight is roughly estimated at 50 tons, and its only rival is the meteorite of Anighito, Greenland, to which a recent estimate has assigned a weight of 464 tons. The three meteorites most nearly approaching these are those of Bemdego, Brazil, 53 tons; of San Gregorio, Mexico, 114 tons, and Chupaderos, Mexico, 152 tons. The dimensions of the Bacu- birito meteorite were measured, after extensive excavations of the soil in which it was nearly imbedded, as follows: length, 13 feet 1 inch; width 6 feet 2 inches; thickness, 5 feet 4 inches. The shape is extremely irregular, being compared to that of a ham; the cubic contents consequently could be only approxi- mately estimated. In composition, an analysis by Whitfield has shown it to contain about 7 per cent nickel, and its structure is eminently octahedral. The exterior shows little oxidation and the pittings are clean and sharp in outline. It is to be hoped that the Mexican Government, which with admirable liberality has already transferred to the School of Mines, Mexico, five of her largest meteorites, may also undertake the similar protec- tion of this unique mass. 5. The Origin of Eskers; by W. O. Crossy. Baston Soc. Nat. Hist., vol. 30, No. 3, pp. 375-411.—It is an accepted truth among glacialists that eskers are formed either by super- glacial or subglacial streams, and the large majority of geologists believe they are of subglacial origin. Professor Crosby has reéxamined the whole subject and concludes that streams flowing upon the ice sheet rather than those flowing under it are respon- sible for most of the esker ridges. 6. Ueber Hussakite (Xenotim) und einige andere seltene gesteinbildende Mineralien ; by H. Roster. Zeitschr. f. Kryst., XXXvl, pp. 258-267.—Prismatic xenotime (hussakite) has been identified in the heavy residues of a large number (52) of European rocks and kaolins amongst the crystals usually referred to zircon, from which it was distinguished in part by the applica- tion of the magnesium test for phosphoric acid ; in part by the hepar reaction for sulphuric acid with soda on charcoal, but for the most part by the difference in the strength of the double refraction in microscopic preparations. Owing to the elusive nature of all these tests when applied to microscopic crystals in microscopic quantities, it seems desirable to carefully verify these identifications before conclusions of such far-reaching conse- quences be definitely accepted. | Contrary to the observations of Derby, who only identified prismatic xenotime in a single case in scores of residues examined and who found the octahedral forms almost invariably accom- panied by monazite, the author finds, in the rocks examined, the Miscellaneous Intelligence. ; 317 prismatic forms of xenotime more abundant and widespread than the octahedral one and than monazite as well. In addition to zircon, xenotime and monazite the author found anatase, regarded as secondary, in about half of the residues examined ; dumortierite in two kaolins from 2-mica granite ; chrysoberyl in seven kaolins (6 2-mica granites and 1 syenite) and one fresh 2-mica granite; staurolite in two kaolins from aplite, and andalusite in five kaolins from 2-mica granites. III. MisceLLANEOUS SCIENTIFIC INTELLIGENCE. 1. International Catalogue of Scientific Literature. First Annual Issue. M. Borany, Part I, May, 1902. Pp. xiv, 378. D. Cuemistry, Part I, June, 1902. Pp. xiv, 768.—These two volumes of the first annual issue of the International Catalogue of Scientific Literature, commencing with the year 1901, have recently appeared. This Catalogue is published for the Inter- national Council by the Royal Society of London, being an out- growth of the well-known Catalogue of Scientific Papers relating to the scientific literature of the Nineteenth Century, published by the same Society. In the form which the plan has finally taken, each complete annual issue of the Catalogue will consist of seventeen volumes, one for each of the sections of science sepa- rately recognized, The set will be sold to the public for £18, individual volumes costing, according to size, from ten to thirty- five shillings. The director is Dr. H. Forster Morley, whose address is at the Central Bureau, 34 and 35 Southampton st., Strand, London, W.C. ‘Twenty-nine Regional Bureaus have been arranged for, which are to furnish the material for the Cata- logue ; for the United States, communications are to be sent to Prof. 8. P. Langley, Smithsonian Institution, Washington. The method of classification and indeed all the details of the entire plan have been very carefully worked out, but only the outline can be given here. Each of the volumes issued consists of three parts: (a) Schedules and indexes in four languages, English, French, German and Italian; (0) an author’s catalogue ; (c) a subject catalogue. The subject catalogue is divided into sections, each of which is denoted by a four-figure number between 0000 and 9999. ‘These numbers follow one another in order but all are not used, space being left for such additions to the system of classification as may be found necessary in future years. In the case of the two volumes now published, the material for 1901 being yet incomplete, the first part will be followed by a second part in a few months; in future, however, when the organization is complete, it 1s planned to issue a single annual volume only for each subject. The breadth and completeness of this great scheme for putting within the reach of every worker in science a catalogue of all original contributions on the subject in which he is interested, in whatever form or place published, is worthy of the century with Am. Journ. Sct.—Fourta Series, Vou. XIV, No. 82.—Octoprr, 1902. 22 318 Scientific Intelligence. which it commences and the Society under whose auspices it is published. It is to be hoped that the undertaking may not only receive all needed financial support, but also that editors and authors may inform themselves minutely as to the details of the plan, so that they may prepare subject-indexes for all papers at the time of their publication, thus diminishing very largely the subsequent labors of the collaborators. , 2. British Association.—The annual meeting of the British Asso- ciation for the Advancement of Science was held at Belfast dur- ing the week beginning September 10th. The meeting is de- scribed as having been very successful, about equal in numbers to that held in the same place in 1874, when the attendance was 1,951. The address of the President, Professor James Dewar, was of the highest interest (see Nature of Sept. 11), dealing, in addition to some general topics, with the subject of low tempera- ture and the liquefaction of gases, to which he has personally contributed so much. We quote at length from the address in another place. 3. Haperiments in Aerodynamics ; by 8. P. Lanatry. Second edition, pp. 115 with ix plates. Washington, 1902. (Smith- sonian Contributions to Knowledge, No. 801.)—This volume is essentially a reproduction of the first edition of this interesting memoir, which was issued in 1901 and noticed in this Journal in November of that year (vol. xlii, p. 427). Since its first publi- cation, machines made on the principles here described have actually flown, which fact gives a practical interest to the sub- ject; a description of the heavy steel flying machines is promised for some time in the future. 4. Elementary Physical Geography ; by Witt1am Morris Davis. Pp. x, 401, with numerous maps and illustrations (Ginn and Company.)—It is a pleasure to note the publicat.on of a text-book which presents a subject in an interesting elementary form without the loss of scientific accuracy and a rational mode of treatment. Professor Davis’s new text reduced from his «Physical Geography ” is just such a book. 5. The International Quarterly.—The International Monthly, which since January, 1900 has had a highly successful career under the editorship of Mr. Frederick A. Richardson (Burling- ton, Vt.), will hereafter be continued as a quarterly with the same editorial direction. Each number will be more than double the size of the monthly, and will present articles of live interest by able writers at home and abroad. ‘The September issue (pp. 1-214) of The International Quarterly begins vol. vi, of the series. OBITUARY. Proressor RupotF Vircuow, the illustrious German anato- mist, physiologist and anthropologist, the founder of cellular pathology, died at Berlin on September 5, in his eighty-first year. Plate VIII. XIV, 1902. iz Vol; Se Am. Jour. NN ‘48800 SUOT[V SepI[spuv] [BOOT ‘ALVIS GNOWHORT WOWd ‘LNHONTA “LG ‘aUgIuaAOg wT *1O[ABT, “WT ‘O AQ ydvisojoug Pe Ei AMERICAN JOURNAL OF SCIENCE [FOURTH SERIES.] Art. XX XIII.— Observations on the Evuptions of 1902 of La Soufriere, St. Vincent, and Mt. Pelee, Martinique ;* by -Epmunp Oris Hovey. THE chain of islands bounding the Caribbean Sea on the east, and known as the Leeward and Windward Islands, the Lesser Antilles or the Caribbean Islands, are almost wholly of voleanic origin, the most important exception to this rule being Barbados. From Grenada northward the chain of vol- canoes extends in a grand curve for about five hundred miles, with its convex side toward the east, indicating a line of weak- ness in the earth’s crust comparable with those which are out- lined by the festoons of volcanoes along the northern and western coasts of the Pacific Ocean. The volcanic nature of these islands has been known ever since they first were explored, but only a few eruptions have been recorded during the past four centuries—the most important being those of La Soufriere on St. Vincent in 1718 and 1812, with Mt. Pelée on Martinique in slight eruption in 1851. Continuous solfataric action, which sometimes has been quite violent, is known in the crater of Mt. Misery on St. Kitts, the “ Soufrieres” of Guadeloupe and St. Lucia and the Boiling Lake of Dominica. Hot springs have been a feature of several localities on Martinique, St. Vincent and other of the islands. : La SouFRIERE, St. VINCENT. At least as early as April, 1901, earthquakes became more frequent and noticeable than usual in St. Vincent, but, with * The author was sent to the islands of Martinique and St. Vincent as the representative of the American Museum of Natural History, New York, to study the phenomena connected with the recent eruptions. The article here published is a condensation of the ‘‘ Preliminary Report” prepared for the Museum authorities and published in the Bulletin of the Museum, vol. xvi, pp. 3383-372, pls. xxxili-li. The author’s field work on the islands covered the period from May 21 to July 6, inclusive, and his Report and this article pertain almost solely to the personal observations made during that time. Am. Jour. Sc1.—FourtH Series, Vou. XIV, No. 83.—NovemBeEr, 1902. 23 320 FE. O. Hovey—Eruptions of 1902 of La Soufriere, oe Petit Balejnéi4 DuVal lgs Pt( OX 7 BS 9 1 Rabaka Sepa eal) Gy R j ey SOK, 4 Dry River. | Le Chateaubelait\ SS) Georgetown. Y/ f May 27 Zax June 3m 10 5 English Miles. Fic. 1. Map or tHe Isuanp or Sr. Vincent, B. W. I. The cross-lined area shows approximately the portion of the island which was devastated by the May, 1902, eruptions of La Soufriére. The violent outburst of September 3-4 deposited much additional material on the lee- ward (west) side, and extended the zone of devastation about four miles south of the boundary here indicated for that side of the island. The dot- and-dash lines show the principal routes traversed by the author while on and near the voleano. St. Vincent, and Mt. Pelée, Martinique. 321 the exception of Mr. F. W. Griffith, of Kingstown, no one seems to have connected them with an impending eruption of the Sonfriére. In December of that year, however, the people living on the western slopes of the voleano began to feel anxious on account of the subterranean noises heard occa- sionally. By February, 1902, the rumblings had become so frequent that the inhabitants were very uneasy and began to leave the district, so that but one person was left within the fated area when the great eruption of May 7 occurred. The rumblings were less distinctly heard on the eastern or wind- ward side of the island, and the warnings were not heeded so generally, because it was: supposed that the prevailing winds would carry to westward any ejecta from the crater, in case of an eruption. The loss of life was confined to the windward side of St. Vincent. ; The first ascent of the Soufriére, since the eruption of May 7, 1902, was made on Saturday, May 31, by Dr. T. A. Jaggar, Jr., George Carroll Curtis, T. MacGregor MacDonald* and myself with six porters. We went up from the site of Walli- bon village, on the leeward (west) side, following the remains of the old trail to the rim of the crater at 2790 feet above the sea, an elevation obtained by taking the mean of the readings of three aneroid barometers.t We found the crater unchanged in diameter, as nearly as Mr. MacDonald could tell, and there- fore to be about nine-tenths of a mile in diameter from east to west and eight-tenths of a mile from north to south, judging from measurements made on the map. The beautiful crater lake, for which the Soufriére was famous before the eruption, had disappeared of course, but there was a small Jake of boil- ing water in the bottom of the pit, from the southeastern quarter of which steam was ascending in a strong column. See figs. 4 and 5, p. 351. This column at intervals was carry- ing up quantities of black sand with it to moderate heights above the bottom of the crater. We estimated the surface of the boiling lake to be about 1600 feet below the point on * Mr. MacDonald is the owner, with his brother, of several estates on the leeward side of St. Vincent. One of these was destroyed in the May erup- tions, and three others suffered the loss of their growing crops through the outburst of September 3. Mr. MacDonald had the presence of mind to remain in one of his honses, the Richmond Vale estate, from which there was an uninterrupted view of the npper portion of La Soufriére, and to take notes in detail of what happened on May 7 up to the time of the great erup- tion which took place at 2 Pp. M., when he fled for his life. His notes have been published in full in the Kingstown Sentry of May 16, 1902, and in the - Century Magazine, vol. lxiv, pp. 638-642, August, 1902. + All the altitudes recorded in this article were obtained by means of aneroid barometers, except as otherwise stated in the text. { For convenience of printing, the views iliustrating this article have been pJaced together on pp. 351 to 358. 322 E. O. Hovey—Eruptions of 1902 of La Soufriére, which we were standing, and 2400 feet below the highest point of the rim. The lake seemed to be shallow, judging from some nearly flat ground in the bottom of the crater northeast _of the water. The surface of the old crater lake was 1930 feet (chart) above tide. Its depth in the center was 874 fathoms, according to the statements of P. F. Huggins, engi- neer, of Kingstown, St. Vincent, who told me that he sounded it in 1896. His line was too short to reach bottom in the northwestern part of the lake. Almost directly opposite the point where we first reached the rim was the saddle between the “Old” crater and the crater of 1812, apparently unbroken by the eruption. From the lower third of this nearly vertical rock-face there issued a strong stream of water which cascaded down the precipices and flowed across a rather narrow strip of nearly level ground in the bottom of the crater and emptied into the boiling lake. It seemed as if this stream must be the discharge of the waters now collecting in the crater of 1812, itself the possessor of a little lake before the eruption of the present year. The western side of the crater rim showed a gash on its western side, leading into the Larakai Valley, but the bottom of the gash was more than a thousand feet above the bottom of the crater. Mr. MacDonald said that the gash was there before the eruption took place, but that it seemed to him to have increased in size since the outbursts began. The gash is very much smaller than that in the southwest side of Mt. Pelée, and it does not seem to have had any appreciable, or, better, any determinable, effect in concentrating the force of Soufriére’s voleanic hurricanes. Tremendous avalanches of rocks and earth descended the inner precipitous slopes of the crater at intervals during our stay on the rim. They made a great deal of noise, and probably occasioned some of the “groaning” of the volcano reported by the islanders. On June 4 Jaggar, Curtis and I made an attempt at the ascent from the windward side. We reached the altitude of 3200 feet, but turned back without getting to the crater itself, on account of dense trade-wind clouds. On June 9 Curtis and I made our third ascent, alone, except for one guide, and reached the rim of the crater on the southeastern side two or three hundred yards beyond the spot at which we had turned back on the preceding occasion. For fifteen or twenty yards back from the edge of the rim in the ground there were crevices many yards long and up to three inches wide, which formed lenses with the edge itself and indicated the imminence of landslides into the crater. We pushed along the rim north- ward, until, at an altitude of 3550 feet above the sea, we stood - between the large crater and the crater of 1812. The summit St. Vincent, and Mt. Pelée, Martinique. 328 of the Soufriére east of the large crater and south of the small one is formed bya rather small plateau which slopes gently toward the southeast, closely analogous in position to the small high plateau on Mt. Pelée. This platean was covered with a bed of dust, Japilli and bowlders which was ten and fifteen feet thick in places, and the trenches cut by recent rains made traveling very laborious, except near the edge of the crater. In spite of clouds and rain, this visit, through occasional glimpses of the interior, enabled me to determine that the crater of 1812, which for nearly a century has gone by the name of the “ New” crater, took no active part in the erup- tions of May of the present year, a conclusion based on the following considerations: the saddle between the two craters appeared to be intact, confirming the observations made from the other side of the large crater; a knife-edge ridge which ran at a steep incline from the saddle to the bottom of the small crater and formed the pathway for descent into it before the eruption, was still there, and had on its slopes bare trunks of trees standing; in the bottom of the crater along the base of this ridge one could see talus slopes of dry (?) dust and Japilli which had slid and rolled down its sides; although the roaring of the steam and boiling water nearly half a mile below us in the large crater was obtrusively discernible, no sound whatever came from within the crater of 1812; the rim of the small crater showed less and less dust as one receded from the edge of the great crater. Samuel Brown, a ranger, or caretaker, on the Lot 14 estate on the southeast slopes of the Soufriére, who was our guide when we reached the small crater,, told us that he watched the eruption of May 7 until the oreat outburst at two o’clock and that no cloud of steam or “smoke” rose from the small crater. Furthermore, at the time of my leaving the island, June 10, no column of steam had risen above that crater since May 7. Brown was at the sugar factory of the estate, three and one-half miles in a straight line east-southeast from the crater, a most favorable spot from which to observe what was going on at the summit of the mountain, and he saved his life by running into the rum cellar of the factory and closing the door and ‘the window shutters just before the volcanic blast swept over the building. Inquiry in Georgetown found persons who had watched the eruption from the town and had noted the fact that no column of steam rose from the small crater. The Soufriére, and, in fact, the whole of the island of St. Vincent, is made up of ancient lava flows alternating with vol- canic fragmental deposits or tuff agglomerates.* These ancient * The alternation of lava beds and tuffs is well illustrated in fig. 5, p. 351. 324 EL. O. Hovey—Eruptions of 1902 of La Soufrisre, agelomerates show that there have been many eruptions of the volcanoes of St. Vincent of the same character as that of 1902. They contain bombs as well as blocks. The beds of solid rock on the island show that many of the ancient eruptions were accompanied by extensive flows of molten lava. The porous agolomerates have suffered much from the decomposing action of percolating waters, and the lava beds show extensive altera- tion due to the same agency. Beautiful spheroidal weathering is common in the basalts of the southeastern part of the island and in the elevated beach conglomerates of the windward coast. Although there are many ancient lava beds in the composi- tion of the mountain, no stveam of melted lava has issued from the Soufriére during the present eruption. The “ bread-crust ” bombs, however, which occur plentifully on the mountain sides, especially on the windward slopes, show that during the present eruption molten lava has been present in the throat of the vol- cano, and that many lumps of half-melted rock were thrown into the air. Besides the bombs, the volcano ejected blocks of ancient andesitic lava of several kinds and of varying degrees of coarseness of grain, and of all sizes up to masses six or eight feet across, and vast quantities of coarse and fine lapilli and dust. Most, if not all, of the blocks were thrown out at very high temperatures, as is shown by their cracked condition, though they were not actually fused. Although a few bombs, some of which were twelve to fifteen inches across, were found on the leeward side as far away from the crater as the site of Richmond village, three and one-half miles distant, by far the largest number of both bombs and blocks, as well as the largest specimens, were found on the windward side, bombs fifteen to eighteen inches in diameter being common in the bed of the Rabaka Dry River. The area of devastation on St. Vincent is very large in pro- portion to the total area of the island. After plotting it out carefully on the British Admiralty chart and measuring the area with a planimeter, I find it to be forty-six square miles, practically one-third the entire area of the island. From much of this devastated area, however, the ashes are being washed off so rapidly by the rain that vegetation is already asserting itself, and within another year crops will be growing there again.* Extensive landslides have taken place on the western side (see Plate VIII), removing a strip of coast, in places one * Newspaper reports and private advices from St. Vincent show that the area of devastation has been extended on the leeward side of the island by the tremendous eruption of September 3-4 about four miles south of the boundary indicated on the map herewith presented (fig. 1), while the whole western portion of the devastated area got a heavy additional coat of lapilli. The windward side did not suffer materially from this eruption. St. Vincent, and Mt. Pelée, Martinique. 325 hundred yards wide, continuously from the mouth of the Wallibon River to Morne Ronde village, a mile and a half to the north, and at intervals for two miles farther north. These landslides have left precipitous walls along the shore-line, and deep water is found where villages stood and prosperous plan- tations existed before the eruption. We had no sounding line, but our boatmen could not touch bottom with a twelve-foot oar three feet from shore on the site of Morne Ronde village. The sections left by the slides show that the land which has disap- peared consisted of delta and coast-plain deposits, material which would easily be shaken from the more substantial lava flows and agglomerate beds by the vibrations due to the erup- tions. The eastern, or windward, side of the island is not nearly as steep as the leeward, and landslides have not occurred there as features of this eruption. On the contrary, the wind- ward shore-line from Black Point, a mile south of Georgetown, northward almost to Chibarabou Point, more than six miles distant, has been pushed out by the vast quantities of fresh Japilli which have been brought down from the slopes of the volcano by the rivers and the heavy rains, during and since the eruptions, and distributed by the ocean currents. A large amount of material, too, was brought down by the Rabaka Dry River an hour in advance of the great outburst of May 7, which seems to have been due to the bodily discharge of a portion, at least, of the old crater lake into the headwaters of that stream. Survivors who attempted to cross the Rabaka Dry River toward noon of that day report that they were prevented by a torrent of “boiling hot” water and mud rush- ing down the valley, and that.a wall of water and mud fifty or more feet high (they compared it with the height of a fac- tory chimney) came out of the upper reaches of the river and swept out to sea. There was no heavy rain that day before the eruption took place, but the lake still was in the crater early in the day, according to the tale of a fish-woman who had ascended the mountain from Gecrgetown that morning on her way home to Chateaubelair. The trail led along the rim of the crater for half a mile. The woman reached the rim at nine o’clock and found that fissures had appeared in the ground and that the lake was at a higher level than usual and boiling. She rushed back to Georgetown to warn the people, but her tale was discredited. Mr. MacDonald’s notes contain the entries: “12.55 p.m. Enormous discharge to windward side, color darker. 1 P. M. Tremendous roaring, stones thrown out to windward thousands of feet.”* While this does not prove the bodily outthrow of the lake, it shows that there was * Century Magazine, vol. lxiv, p. 630, August, 1902. 326 EL. O. Hovey—Eruptions of 1902 of La Soufriére, a great outburst from the crater just in advance of the flood in the Dry River Valley. It is evident that there was a blast or a series of blasts of hurricane violence from the crater of the Soufriere as well as from that of Mt. Pelée, as a feature of the eruptions of 1902. The effects were not so appalling, however, on St. Vincent as on Martinique, because no large city was destroyed there. The overturned trees constitute the principal evidence on the island of St. Vincent. They all point away from the crater, except for slight modifications due to local topography (see fig. 10). The blast extended radially in all directions from the crater, suggesting the explanation that some great vol- ume of steam, rising from the throat of the volcano, could not find room for expansion upward, on account of the column of steam and ashes which had preceded it, and the ashes fall- ing therefrom, and that it expanded with explosive violence horizontally and downward, following the configuration of the mountain. This accords with the testimony of Mr. MacDonald and other eye-witnesses of the eruptions, who say that they saw the clouds of “smoke” (dnst-laden steam) rushing down the sides of the mountain with terrific speed. This dust-laden steam was able to do much work of erosion, as is shown by the horizontally scoured sides of some of the exposed cliffs and by the trunks and roots of trees. The roots particularly have been charred by the heat and have been carved into fantastic, pointed shapes, as if they had been subjected to the action of a powerful sand-blast. Erosion has not materially affected the original surface of the ground as yet, because almost every- where one can find the living roots and charred blades of grass and other vegetation beneath the covering of dust and lapilli, the first of which acted as a protection against the heat of the rest. Now, however, the heavy rains “take up vast quantities of the loose lapilli for use as a powerful scouring agent in attacking the denuded hillsides, and thus old valleys are being deepened and widened. The particular feature of the May eruptions of the Soufriere was the enormous amount of dust* which was thrown into the air and distributed over a vast circle or ellipse the area of which cannot yet be calculated for lack of data. The British steamship Coya had an eighth of an inch of volcanic dust * The following chemical analysis is of dust from the May eruptions which I collected May 27 in a room in the Langley Park estate house, ahout one mile north of Georgetown, St. Vincent, in which twenty-one dead bodies were found after the eruption of May 7. The analysis was made by Dr. W. F. Hillebrand of the United States Geological Survey, to whom my acknowl- edgments are due, and is the unpublished analysis referred to in his article in the National Geographic Magazine for July (vol, xiii, p. 297) as empha- sizing the greater amount of sulphur present in the ejecta of La Soufriére St. Vincent, and Mt. Pelée, Martinique. = — 327 from this voleano fall on her deck when she was two hundred and seventy-five miles east-southeast of St. Vincent. The steamer encountered the dust at 10.30 Pp. m., May 7, eight and one-half hours after the eruption of the Sonfriere began, indicating trans- port against the prevailing surface wind at more than thirty-two knots per hour. Reports of vessels from the west (leeward) of the island are curiously lacking. The dust was spread like a gray mantle over the island, generally diminishing in thick- ness from the crater outwards, but collected in vast deposits in certain valleys on the sides of the mountain, where the condi- tions seem to have been particularly favorable. The chief of these beds were formed in the Wallibou, Trespé and Rozeau valleys on the leeward side, and in the valleys of the Rabaka Dry River and its tributaries on the windward slope, with by far the greatest thickness along the Wallibou and Rabaka Dry Rivers. In the valley of the Wallibou the deposits were not less than sixty feet deep in places, while in the Rabaka Dry River the fresh material filled a gorge which is said to have been two hundred feet deep before the eruptions began (see fig. 9). From a distance this deposit looks as if it were a glacier coming out of the mountains. Such great aceumulations of hot Japilli and dust retain pee heat for a long time and they have given rise to secondary, or superficial, eruption phenomena of striking character and con- siderable interest. The river water and the water from the than in those of Mt. Pelée. The absence of chlorine is interesting as indi- cating fresh waters as the source of the steam of the eruptions. y) by) 9 Ou ato cds 9) oy) oy) by) 9) 99 9) 9) 99 93 29 >) 99 99 9 GG GG iss O& O€ O& GG 06 OV OF OF LL-T ‘18 ‘ds 0g eUld “TAye4y 10H OO00T-0O OOOT-0 OOOT-0 OOOT-O OOOT-0 OOOT-O 000€-0 0008-0 0O00T-0 OO0T-0 OOOT-O 0090-0 UIs "Ua ye4y "OATHN Acid (ZG of Vanad don O Gooch and Stookey—Leduct 3874 "m90Ly tf “09° A F000-0 0} JuayeAinbo ag Avs AgTy YA 10 [OH pozerzuoouoy yA on[q onpised ” g ” ¢: SoyNUlU OZ po[log “O'A 1000-0 07 4U9] -vAInba 1g OAV IGY YAM poyvoi, onpiser 9) 99 ” ” 99 99 ssoudip 0} poyeiodeaq sayNUIUL GT poplog TOT pee -U90U0D YIM poejvor}, UoYyAM UMOIG oONpIset 3) 9 3) 9). ssoudip 07 poyerodeaq ‘qUOTAYvEIY FO S[IejJod ‘ong + 41000-0 46200-0 ¥£900-0 40100-0 Udy te Ba 6900-0 ¢L00-0 ‘ulIs “LOLLA ‘TI aTav T, 9) ” 6910-0 9? 9 6910-0 "TIS “peye[noleo 207A “UMOIg x 9) {sex Oe oS: ms OF ” ” tL ” oy) xh ” ” xh OG: a0 eas OF ” ” G ” ” *G OMT PLease sec0T ‘Ua ye} IOH OOOT-0 OOOT-0 OOOT-0 "UIs "Ma yey °OA°HN by the Action of Hydrochloric Acid. Y 8% of the first action weakened by boiling. Plainly two methods of bringing about the re-treatment with strong acid are open: either the weak acid remaining after the boiling process may be wholly removed by evaporation and replaced by concen- trated acid, or it may be cooled and re-saturated with gaseous acid. Table II contains the record of results obtained in both these ways. These experiments show very clearly that several successive treatments with strongest hydrochloric acid, consisting either in the addition of the concentrated aqueous acid to the dry residue in successive portions, or in passing gaseous acid through the residual liquid cooled in ice-water, finally bring the residue to a condition of reduction in which the recharging of the liquid residue with gaseous acid produces no brown or green color but a clear blue. When this condition is reached the Holverscheit procedure produces no appreciable further reduc- tion. The holding of the blue color when the solution cooled in ice-water is thoroughly charged with the gaseous acid, appears to be the best evidence of the complete reduction of V,O, to _V,O,; it is not sufficient that the boiled solution, in which the acid has been weakened, should be blue. In the several manipulations of the repeated processes there is likely to be some mechanical loss of chlorine. For this reason, the direct titration of the residues by potassium per- manganate in presence of a manganous salt was combined, as a control, with the determinations of the iodine set free by chlorine in the distillate, as shown in the experiments of Mable Til... -. In these experiments we have again evidence that it is pos- sible to effect the reduction of vanadic acid to within a few per cent of the amount present by a single treatment with con- centrated hydrochloric acid, and that the amount of the reduc- tion may be determined by titrating the residue with potassium permanganate. It is plain, therefore, that Gibbs’ application of this mode of reduction and titration to the determination of the small proportions of vanadium pentoxide found in many of the complex salts studied by him is also justified. The experiments show also that when the action of hydro- chlorie acid is sufficiently continued, ordinarily large amounts of vanadic acid may be completely reduced to the condition of the tetroxide; and the method of reduction is of special advantage in those cases which eall for titration of the tetrox- ide by permanganate, since in such cases the use of Holver- scheit’s admirable method of reduction by hydrobromic acid is precluded. Am. Jour. Scl.—FourtTH SERIES, Vout. XIV, No. 83.—NOVEMBER, 1902. 376 NH,VO; erm. 0°1000 0°1000 0°1000 0°1000 0:1000 0°3000 0°3000 0°3000 Gooch and Stookey—Reduction of Vanadic Acid, ete. Aq. HCl em?, 25 sp. gr. 1°20 95 ce ce 25 66 (7% 30 sp. gr. 1°20 Gast 25 sp. gr. 1°20 Gast Gast 25 sp. gr. 1°20 Gast Gas{ 25 sp. gr. 1°20 Gast 25 sp. gr. 1°17 Gast Gast Gast Gast V2.0; calcu- lated. erm. 0°0765 0°0765 0°0765 0°0765 ---+- 0°0765 TABLE III. V205 found by chlorine in distillate. germ. \=-s-+ 00711 0°0734 0°0714 0°0746 0:0765 0°2259 0°2288 0°2207 0°2244 0°2258 0°2269 0°2281 * Residue after boiling was blue. + Residue blue after boiling was still blue when re-saturated. t Residue was cooled in ice-water and re-saturated with gaseous HCl. Error. erm. e-~-= ---- 0°0036 0°0007 0°0088 0°0051 0°0037 0°0026 0°0014 V205- found by — KMn0O, as residue. Error. grm. 0:0025 — 00029 — 0°0021— 00007 — 0:'0000 0:0011— 0°0007 + a John Wesley Powell. 377 JOHN WESLEY POWELL, Founder and Director of the Bureau of Ethnology of the Smithsonian Institution, for thirteen years Director of the United States Geological Survey, died at Haven, Me., Sep- tember 23d, in his sixty-ninth year. Althongh well known locally for his seientifie work and enthusiasm before the civil war, and acquiring military repn- tation in that war, he first came prominently before the scientific world and the wider general public by his daring exploration of the great Colorado Canyon in 1869, and since that date has been a conspicuous personage among American scientists for his zeal for science, his eminent administrative ability—shown in the organization and management of geo- graphical and geological surveys and scientific bureaus—his broad grasp of scientific questions, his varied activities in the promotion of research in several branches of science, and by a charming personality. He was born March 24th, 1834, at Mount Morris, then a small village in the Genesee Valley of Western New York. His parents were English, his father a Methodist clergyman who came to this country but a short time before the birth of his son. The requirements of his profession caused many changes of home, and the family moved to Ohio in his early childhood ; eight years afterwards to Wisconsin; and again, when the boy was fifteen years old, to Illinois, which was young Powell’s home until the breaking out of the civil war, in his twenty-seventh year. | The boy was an ardent lover of nature and the migratory home of the family during the days of his youth and early manhood gave him unusual facilities to see outdoor nature under many aspects, but the conditions of his environment were very unfavorable for obtaining a college or university training. He was fond of roaming, a keen observer, and in his studies was from the first strongly attracted to the natural sciences, especially such of them as could be pursued out of doors. He studied botany and geology and used every opportunity to learn these and the kindred sciences. He was fora while in the Illinois College at Jacksonville, later in Wheaton College and still later in Oberlin College in Ohio. Unable to attend any of these continuously, he alternated between teaching school and studying when and where the opportunity occurred. To him there was no continuing curriculum or studies available and, looking to an academic degree, he studied as the opportunities offered, now while teaching in some country or village school, then as a temporary student in some college, or,while roaming. 378 John Wesley Powell. He made excursions and collected specimens which found their way into the museums of the several colleges and soci- eties with which he had: been connected. Some of these excursions are noteworthy. He journeyed to St. Paul on the Mississippi and across Wisconsin to Mackinaw. In 1856 he descended the Mississippi alone in a row-boat from the falls of St. Anthony to its mouth, making collections on the way. In 1857 he rowed the whole length of the Ohio River, from Pittsburg to its mouth, and in the fall of that year studied the geology and mineralogy of the Iron Mountain Region in Mis- souri. In 1858 he made a trip down the Lllinois River to its mouth, and up the Des Moines River, returning, as usual, laden with specimens. Meanwhile he had become a member of several local scientific societies as well as colleges. These institutions had given him much encouragement and some facilities in the pros- ecution of journeys, but this encouragement was moral rather than pecuniary and the necessary funds for the excursions— explorations we may call them—he was obliged to earn for, himself by teaching during a portion of each year. All this brought him into acquaintance with a great variety of people, scientific and otherwise, and the experience was rich in incident and adventure. I have some most pleasing recol- lections of the charming way in which he recounted some of these experiences to his intimate friends; of the enthusiasm and humor with which the stories were told, and the touches of philosophy with which they were embellished. Such was the great university where he was educated. What a training it was for his future career! It often required as delicate tact, as careful diplomacy, as ingenious planning and skillful management, as enthusiastic argument and as per- sistent effort to carry out his plans to success, as it did later to deal with politicians in and out of congress and to successfully carry out the great works with which his name will be asso- ciated so long as science shall be studied. Those row-boat excursions on the gentler currents of the Ohio, Mississippi, and Illinois, were the forerunners of the daring one through the madly rushing waters in the great canyon, and the plans of the great Geographical and Geological Survey of the nation had their elements in these earlier trips. His school changed when the great rebellion broke out. He enlisted as a private in the army and rose through the successive steps of lieutenant, captain, and major, in which office he lost his right arm at the battle of Shiloh. As soon as he recovered he returned to his post and continued in the service until the very end. He was made lieutenant-colonel and in the last days of the war received the commission of colonel, John Wesley Powell. 379 which he declined, not wishing to enter the profession of war, but the military title of major clung to him through life. His war experiences may here be considered as a sort of post- graduate study, following the gentler training of previous years, a schooling, both as private soldier and commander of a regiment, a training in the management of men in both field and office, and for bolder exploration. The war over, he refused a lucrative civil position in his own town, as he already had a higher military one, and accepted a much less remunerative position as Professor of Geology, and Curator of the Museum of the Illinois Wesleyan University at Bloomington, which was followed later by a similar position in the Illinois Normal University. In 1867, Professor Powell visited the Rocky Mountains of Colorado, taking with him his class in geology, for the double purpose of exploration and research, and for the instruction of his students in field work. He was practically the pioneer in the actual and practical introduction of extensive expeditions with students as a part of their college training for future field work, a phase of college instruction since so extensively prac- ticed and which has been so rich in results. Major Powell, on this excursion, became interested in the Colorado Canyon and its surroundings. For a century or more vague rumors of this region and its wonders had reached the outer world: stories of its awful and mysterious chasms, abso- lutely impassable and entirely preventing passage over the region. The stories became much more numerous and the information more definite after 1850, when the gold-seekers attempted to reach California; but curiously little was accu- rately known more than that the waters of the Rocky Moun- tains, from as far north as the 48d parallel, found their way through an awful canyon hundreds of miles in length to the borders of California and thence to the Gulf. It was reputed to be many thousands of feet deep. One and another had been on its brink here and there; that was about all, except the disappearance of luckless travelers who had by accident, got into it at certain points. In 1868 Major Powell organized a little party of movufntain- eers and others and explored a portion of the region, studied the problem, resolved on the exploration of the canyon, and finally went into winter quarters on the White River. From there he made further reconnaissances and other preparations for the bold work he had planned. The transcontinental railroad, then under construction, had progressed far enough to bring in such supplies and appliances as were not otherwise obtainable, and in the early spring of 1869 the expedition left its winter quarters on White River 380 John Wesley Powell. and proceeded to where the Union Pacific Railroad crosses the Green River. Four small row-boats had been built in Chicago for the specially dangerous voyage and transported on the still unfinished railway to this place. The small party consisted of but ten men. Their make-up is noteworthy. Of his nine companions, Major Powell describes four as having served in the army—in the war recently over; three were described as ‘“‘ hunters and trappers ”— ‘Indian fighters” is incidentally mentioned ; one as “a pen- sive young man;”’ and one was an Englishman “looking for a glorious trip.” With rations sufficient to last ten months, the little fleet started on its perilous trip on May 24th. The departure is briefly chronicled in the narrative. The people at the cross- ing turn out to see them start, he tells us, and “ we raise our little flag, push the boats from shore, and the swift current — carries us down.” They disappear from the outside world and emerge from the mouth of the Grand Canyon August 29, and the next day arrive at the mouth of the Virgin River. But not all of them. Only a few days earlier, the dangers of the passage becoming even greater than before, and a place occurring where it was thought they could get out of the canyon, ahead of them rapids or falls that seemed more dan- gerous than any before encountered, the dark abyss beyond visible but a short distance, three of the men resolved to leave the party while they could. They took out with them duplicate notes, that the results of the trip might not be lost with the party. They made their escape, and along the river below watched for fragments and traces of their abandoned com- panions. Of the voyage itself and its brilliant success, of the results that grew from it, of the adventures and experiences encoun- tered, I need not speak further. The subject forms a brilliant chapter in the annals of exploration and adventure in the interests of science. Never was a bolder voyage planned and executed. I know of no equal in the annals of exploration and navigation. Whilé comparisons between this and polar exploration are difficult, yet, there were in this features of the possibilities which seemed such eminent probabilities of disaster, and the dangers were of such a kind, as to deter the attempt. The disastrous end of the expedition, and the manner in which it would come about, seemed so plain that several of our enter- prising newspapers published more or less minute accounts of its sad end; all of the party but one being lost was the most common plan of the tales; the nature of the dangers were such that one of the party had to be saved or no story written, ex- ee oe | ee ee x John Wesley Powell. 381 cept the disappearance of the party at an unknown time and place. : Some years later, while smoking an after-dinner cigar with some of his friends, he gave his reasons for his faith in under- taking it. I told him that for some years previous to his famous trip, | had been much interested in that canyon and had picked up all the rumors and information pertaining to it that I could, and being in Colorado while he was making the trip was intensely anxious as to his fate, for I thought it was a mad scheme; the canyon was a long and vastly deep one, cut mostly in strata lying relatively level, that owing to unequal hardness the erosion created waterfalls ; that I had been reared in central New York where such waterfalls were especially numerous, cited Niagara and various other examples elsewhere ; that this long and deepest canyon in the world was mostly in such rocks; that he embarked on the river at over 6000 feet elevation, to emerge some 500 or more miles below at nearly the sea level, the river having an average fall of ten or fifteen feet per mile and I had assumed that there must be great falls, and that the explorer must approach them from above. He answered in substance, ‘“ Have you never seen the river? Jt is the muddiest river you ever saw. I was confident that I would find no considerable falls. Rapids I expected, of course, but not falls. I was convinced that the canyon was old enough, and the muddy water swift enough and gritty enough to have worn down all the falls to mere rapids. I entered the canyon with confidence that I would have no high falls to stop us, although there might be bad rapids, and [ believed that we might overcome them in some way,—and we did.” The next year he induced Congress to establish a geological and topographical survey of the Colorado River and its tribu- taries; it was placed under his direction and on it he was en- gaged much of the following ten years. Incident to this, he became interested in the study of the arid regions and the problem of their improvement, also the impounding of the floods of the western rivers for the double purpose of controlling the floods and using the water for irri- gation. The present hydrographic survey of the country is the outcome of his interest in this matter. Between 1865 and 1875 many surveys in the western country were established, acting independently of each other, often in competition as well as rivalry, but not mutually helpful, and working under different departments of government. Major Powell took an early.and active part in the efforts that came up for a more satisfactory adjustment of these and their unification under a more rational system of operation. After much agitation, discussion and opposition, Congress finally, in 382 | John Wesley Powell. March, 1879, discontinued the separate surveys and established the United States Geological and Geographical Survey, under the Department of. the Interior, and Clarence King was appointed Director. Beginning with his first visit to the Rocky Mountains, Minar Powell began ethnological and anthropological studies ‘of the American Indians, for the Smithsonian Institution. Ten years later, in 1876, Professor Henry, the then secre- tary, placed this along with other accumulated material per- taining to this subject in his hands, for arrangement and publication. The next year, his first volume of “ Contribu- tions to- North American Ethnology” was published by the Geological Survey. Later followed five more of these quarto volumes under the same auspices. With the establishment by Congress of the Geological Survey, the Bureau of Anthropology was also established in the Smith- sonian Institution and Major Powell made Director, an office he retained twenty-three years and until his death, and the annual volumes of ‘Contributions’ have continued in the same general form. Mr. King resigned the directorship of the Geological Survey in 1881, and Major Powell was appointed his successor, retain- ing however the direction of the Ethnological Bureau, ‘and for thirteen years he administered both offices, and both institutions were greatly widened in their work and improved in their methods under his administration. In 1894 he resigned the office of Director of the Geological Survey and since then has devoted himself more to other work, ethnological, anthropological, psychological and philosophical. Major Powell was endowed with an eminently philosophical mind, had great administrative ability, was rich in suggestions and fertile in originating and planning, in devising new work and methods and in improving old ones; had a personality of great force, persuasive in inducing men to ‘do, and he inspired the confidence of those with whom he held official or social rela- tions. He was a powerful advocate of reform in laws affecting the permanent welfare of the West and was for many years one of the most conspicuous personages in the scientific corps under the government. He was a member of the National Academy of Sciences and of other societies and clubs, and several colleges and universities conferred academic degrees upon him. Major Powell was a faithful and genial friend, and his most interesting individuality made him many friends. He died of apoplexy. His wife and a daughter survive him. Wm. H. BREWER. New Haven, Conn. Chemistry and Physies. 383 SCIENTIFIC INTELLIGENCE. I. CHEMISTRY AND PHYSICS. 1. The Combination of Hydrogen and Oxygen.—It is well known that many chemical reactions do not take place in the absence of moisture, but heretofore it has not been shown that the combina- tion of hydrogen and oxygen could be prevented in this manner. By using a new method for preparing the gases, the electrolysis of barium hydroxide solution, H. BREREToN Baker has succeeded in obtaining the mixture sufficiently pure and dry to withstand heating to redness without combination. Even when a coil of silver wire was heated to its melting point (over 1000°) in contact with the detonating gas it did not cause combination, but red-hot platinum wire and electric sparks produced explosions. The ordinary ignition-point of these gases is 600°. The interesting fact was noticed that when the tubes in which the experiments were made were subjected to only two days’ drying in the pres- ence of phosphoric oxide, instead of a period of ten days, which was employed for thorough drying, water was formed by heat- ing and combination took place slowly without explosion. This is a result which is entirely different from what takes place, either with the moist or the perfectly dried gases. This beha- vior is explained by the hypothesis that without an electrolyte no chemical action is possible, and that since the water formed by the union of very pure gases is itself very pure, it is not suffi- ciently electrolytic to produce an explosion. During this inves- tigation the important observation was made that hydrogen and oxygen combine slowly when exposed to direct sunlight if they are moist, but do not combine under this influence when they are perfectly dry. The exposure to sunlight took place outside a south window for four months, and the contraction of the moist mixture amounted to one twenty-third of its volume. On account of this result care was taken to dry the gases in darkness in pre- paring them for the experiments which have been described.— Jour. Chem. Soc., 1xxi, 400. snd Wr 2. Arsenic in the Animal Organism.—Several investigators, especially Gautier, have recently arrived at the conclusion that minute quantities of arsenic exist normally in the animal organ- ism, a fact which had been previously denied. The same conclu- sion has now been reached by Brerrranp after a series of very careful experiments. The human thyroid gland, thymus, skin, and other organs, have been found to contain arsenic, but Ber- trand has avoided experiments with human tissues, because it is impossible to be sure that the individuals have not been subjected to treatment with arsenical medicines, or have not been otherwise contaminated with compounds of arsenic. He has also not at- tempted experiments with horses, because these animals are sometimes treated with arsenious acid. Investigations were 384 Scientific Intelligence. therefore carried out with the thyroid glands of calves and swine, then with the bristles of the latter animal, the horns of beeves, the feathers of geese, the hair and claws of dogs, etc. It was soon found that the horny and hairy products contained even more arsenic than the thyroid glands. The horns of oxen gave arsenic in the relatively enormous amount of 5™S per kilo. Traces of arsenic were found in the hoofs, hide, and liver of a calf one month old, while larger quantities were evidently present in the corresponding parts of a heifer 18 months of age, although the horns of the latter contained less of it than those of more mature animals. It appears, consequently, that arsenic accumulates with the age of the animal. As a convincing proof of the normal occurrence of arsenic in an animal which had not breathed air contaminated by industrial fumes, the element was found in the thyroid glands of a seal which was captured in the vicinity of Spitzbergen.— Bulletin, xxvii, 847. H. L. W. 3. Atomic Weight of Radium. —By fractional crystallization of the greater part of the radiferous barium at her disposal, Mux. CuriE has succeeded in obtaining about a decigram of radium chloride which appeared to be perfectly pure. Atomic weight determinations were made with this material with the result that 225 was found to be the atomic weight of the element, assuming that it is bivalent. Radium, therefore, appears to be a higher homologue of barium, with a place in the periodic table under barium and in a line with thorium and uranium. It is stated that pure anhydrous radium chloride is: spontaneously luminous. — Comptes Rendus, cxxv, 161. H. L. W. 4. Double and Triple Thiocyanates.—A number of these com- pounds has been prepared by We ts and his pupils. Most of the double salts contained czsium as the alkali-metal, while ferric, lead, mercuric, cuprous, silver, thallous, magnesium, zine, ¢al- cium and strontium compounds were obtained. It appears that the double thiocyanates are not generally formed in as great variety as the chlorides, bromides and iodides, but most of those obtained corresponded to known double halides. The calcium and strontium double thiocyanates, 2CsSCN:Ca(SCN),-3H,0. and 2CsSCN‘Sr(SCN), .4H,O are of considerable interest, because double salts containing these alkali-earth metals as the negative constituent are very rare. The triple salts show great variety in composition. Several of them crystallize remarkably well, and can be recrystallized from water. Fourteen of these compounds were obtained, belonging to seven different types, as follows: . One salt, ; CsAgZn(SCN),-H,O II. One salt, . Cs,AgZn(SCN), Ill. Five salts, analogous to Cs,Ag,Ca(SCN ),:2 H,O IV. Four salts, analogous to Cs wAg, Ba(SCN). V. One salt, i K Ag, Ba(SCN), ‘H, O Wily One salt, ; : CsAg,Zn, (SCN), VII. One salt, : ; CsAg.Zn,(SCN), eo Ce Chemistry and Physics. 385 The other salts belonging to type III have magnesium, man- ganese and nickel in place of calcium, and in one instance cu- » prous copper in place of silver. The replacements of barium by strontium and silver by copper give the other members of type IV. The four members of the latter type are isomorphous and resemble apophyllite in form.—Amer. Chem. Jour., xxvill, 245. H. L. W. 5. The Determination of Thallium in the Thallous State.—To make this determination THomas adds auric bromide solution in excess to the warm thallous solution, then keeps the liquid warm for eight or ten hours, and finally filters off the metallic gold which is produced and weighs it. Three molecules of the thal- lous salt precipitate two atoms of gold. The test-analyses given are very satisfactory. The method will evidently be useful in analyzing substances containing both thallous and thallic com- pounds.— Bull. Soc. Chim., xxvii, 470. H. L. W. 6. Chemisches Praktikum, von Dr. A. WoLFRuM. 12mo, pp. 562. Leipsic, 1902 (Engelmann).—This volume is the first part, dealing with analytical operations, of a guide in laboratory work. The course is designed ona practical basis with the object of giving the student an idea of factory operations, and of en- couraging the study of technical chemistry. This feature will doubtless appear still more conspicuously in the second part, not yet published, which will deal with chemical preparations. The volume under consideration covers a wide field of analytical chemistry in a very compact form. It embraces a course in quantitative analysis for the common metals and acid radicals, as well as the detection of the more important groups in organic compounds and the application of these tests to a large number of natural and artificial organic products. Quantitative analysis is presented in all its branches; not only the gravimetric and volumetric methods for determining inorganic substances are included, but also the quantitative determination of organic groups, gas analysis, molecular weight determination, toxicologi- cal analysis, and many methods of technical analysis. The methods appear to be well chosen, so that the book will be use- ful, not only to students pursuing courses in laboratory work, but also to analytical and technical chemists. Heb W: Vacuum Thermo Element.—PrtER LEeBEpEw discusses the ae caaces of enclosing a thermo element in rarified air. Kundt and Marbury have shown that a body loses heat less rapidly in a vacuum, and this fact doubtless lies at the root of the superior efficiency of a bolometer or thermo element in a vacuum. The author employs a thermo element of platinum constantin, diam- eter of the wire d= 0°025™". The sensibility steadily increases and reaches its highest point at a pressure of 0°01™™. It is believed that this method will allow measurements of electrical waves, which hitherto could not be made.—Ann. der Physik, No. 9, 1902. pp. 209-213. J. T. 8. Electromotive Force of Ozone.—In the course of an investiga- tion on the possibility of converting the heat of deozonization 386 Scientific Intelligence. into electrical work, A. Branp determined the electromotive force of ozone. The electromotive force of the OQ, and the O, electrode of a Grove gas cell was measured against a normal mercury ele- ment Ce covered with mercuric sulphide), in a normal sul- phuric acid( 3H,SO, g. to the liter). It was found that the electro- motive force with increasing proportion of ozone approached a limit which at 17° was 0°919; at 0°, 0°950 volt.—Anmn.. der Physik, No. 10, 1902, pp. 468-474, Joa 9. Influence of Electrification of the Air on Electric Sparks.— The passage of electricity through a gas is such a complicated phenomenon and is influenced by so many conditions that it is dificult to frame a comprehensive theory of it. Ernst LecHEr shows that a hitherto unknown condition results from electrifying the air or gas through which the electric spark is discharged. For this experiment two sources of electrification are employed. An induction coil produces the spark and a Holtz machine serves to electrify the dielectric. Many interesting phenomena result from this arrangement. The author believes that the phenomena are due to an ionization of the discharge space.—Ann. der Physik, No. 10, 1902, pp. 442-451. 3. T. 10. Onanew Reaction between Electrostatic Tubes and Insulators. —M. W. ve Nicoxarzve believes that certain attractions and repulsions due to an electrostatic field set up in the process of electr olysis form a new phenomenon and confirm Professor Poynt- ing’s theory of the action of tubes of force.— Phil. Mag., No. 19, July, 1902, pp. 133-138. Ji ddd Magnetic Detector for electrical waves.—In a communica- tion to the Royal. Society, of London, Marconr describes his magnetic detector. Ona core of thin iron wires is wound a coil consisting of one or two layers of insulated copper wire, and over this and separated from it by insulating material is wound ‘a second and longer coil. The ends of the inner coil are connected to earth and the aerial conductor ; and the ends of the outer coil to a telephone. The iron core is magnetized by a permanent magnet at one end, which is rotated by clockwork so as to cause a continual slow change in the magnetization. The magnetization lays behind the magnetic force, owing to hysteresis ; but when a high frequency current passes through the inner winding there is a decrease in the hysteresis. A sudden variation in the magnetiza- tion of the iron results, and this results in inducing a current in the coil connected to the telephone. ‘This receiver is more sensi- tive than the coherer. Experiments have been carried out between points 135 miles apart. This detector seems to be Rutherford’s magnetic detector.—Wature, July 31, 1902, p. 334. ba 12. Radiations from Radioactive Substances.—Professor Ruru- ERFORD and Miss Brooks conclude from extended observations that radioactivity is a very complicated phenomenon. Both uranium and radium emit negatively charged particles with high velocities, similar in all respects to cathode rays. Uranium, radium and thorium emit rays which are not deflected by the Ss Chemistry and Physics. 387 magnetic field and are absorbed by gases and thin layers of metal. These rays differ from one another in penetrating power. The emanations from thorium and radium differ greatly in their rates of decay of radiating power. The presence of emanations gives rise to a complicated phenomenon of ‘excited ” radioactivity. Elster and Geitel have recently shown that a negatively charged wire in the open air, free from all possible contamination of radio- active substances, becomes strongly radioactive. This activity decays at a different rate from that due to thorium and radium and is of greater penetrating power.— Phil. Mag., No. 19, July, 1902, pp. 1-28. B os 13. Induced Radioactivity in Air.—lIt has been shown by Elster and Geitel that a strongly electrified wire becomes after several hours strongly radioactive. The authors conclude that the atmos- phere contains some radioactive substance which is attracted to the wire, and that this emanation is like that from thorium. Professor J. J. THomson, however, comes to the conclusion that it 1s not necessary to make this assumption and believes that negatively electrified surfaces may become radioactive without the deposition upon them of substances possessing radioactive properties. He found that a negatively electrified wire placed in a closed vessel, the enclosed air or gas being exposed to Rontgen rays, became radioactive. When the enclosed gas had been bubbled through air the effect was very large. Professor Thom- son thinks that the ionizing power of the wire may be due to a kind of polarization which produces an electric field which makes the wire into a cathode emitting cathode rays of feeble penetrat- ing power, which ionize the gas in the neighborhood of the wire. — Phil. Mag., No. 21, 1902, pp. 352-367. B Peat 14. Deviable Rays of Radioactive Substances.—Professor Rutu- ERFORD and Mr. Grier have discovered that uranium, thorium and radium all emit both deviable and non-deviable rays. They differ from polonium, which does not emit deviable rays. Uranium gives out more deviable rays than radium or thorium. The authors believe that most of the deviable rays are given out by a second- ary product, produced by a disintegration of the uranium or thorium atom or molecule. These secondary products differ from the uranium or thorium in chemical properties.— Phil. Mag., No. 21, Sept., 1902, pp. 315-330. 3. T. 15. Removal of Negative Electricity from the air by falling drops of water.—A. Scumauss shows that there is a possibility that each rain drop passing through higher layers of air rich in ions draws with it negative ions and conveys them to the earth. —Ann. der Physik, No. 9, 1902, pp. 224-237. 5 A 16. Lhe Elements of Experimental Phonetics ; by Epwarp | WHEELER SCRIPTURE. Pp. xvi+627. Charles Scribner’s Sons. Yale Bicentennial Publications.—Valuable contributions have been made by Professor Scripture to the analysis of speech sounds by means of his ingenious apparatus for enlarging and tracing the curves recorded by the graphophone, and his experi- 388 Scientific Intelligence. ments are fully described and a large number of curves given in a series of plates at the end of the volume. The careful analysis of these curves leads to a number of most interesting and impor- tant results, and enables the author to arrive at a definite conclu- sion upon several controverted points, such as the action of the vocal cords, the theory of vowel sounds, the melody and rhythm of speech, the duration of long and short vowels, etc. In regard to the action of the vocal cords, the opinion is strongly main- tained that they do not vibrate like stretched strings or mem- branes, but, at least in the chest register, act by alternately open- ing and closing the orifice between them, somewhat (one would judge) in the manner of a striking reed blown from the wrong side ; the mechanics of such a vibration is not altogether obvi- ous, but, putting aside this difficulty, the hypothesis makes the cord tone consist of a series of puffs of air similar to those pro- duced by a siren, and more or less explosive in character. Many of the curves appear to support this view. One of the conse- quences, however, which the author draws from this theory, and insists upon repeatedly (pp. 41, 94, 97, 263, ete.), cannot be accepted : it is that the cord tone, since it consists of such a series of explosive puffs, cannot therefore be resolved into simple har- monic (sinusoidal) constituents by the use of Fourier’s Theorem. As a matter of fact, a series of explosive increments and decre- ments of the air pressure can be expressed by a Fourier expan- sion, even when the rise and fall are assumed to take place really instantaneously, that is, in a mathematically infinitesimal time, and for however small a fraction of the interval between two puffs the increased pressure endures; if the puffs are all alike and occur at equal intervals of time, then the lowest term in the Fourier series will have a frequency equal to the number of puffs in a second ; if they are not all similar the series will begin with a term of lower frequency, but in any physical case there can be no doubt that the expansion is possible, and any argument based upon the supposed non-harmonic character of the cord-tone will be fallacious. The convenience and utility of such an expansion in any given case is another question. In the discussion of the vowel sounds, some confusion is introduced by this erroneous assumption; but much experimental evidence is adduced in sup- port of the theory of Willis, according to which the resonance tones characteristic of each vowel are fixed in pitch and have no necessary relation to the cord tone, and against Helmholtz’s theory that the resonance tones are always harmonies of the cord tone. Taken as a whole, Dr. Scripture’s work is distinctly interesting as well as instructive ; it is written with spirit and enthusiasm, the illustrations are admirable, and the descriptions of apparatus and of experimental methods are so clear and detailed that it might well serve as a laboratory manual. To the student of phonetics it will of course be indispensable on account of the wealth of scientific material which it contains. H, A. B. Geology and Mineralogy. 389 II. GEroLoGy AND MINERALOGY. 1. United States Geological Survey.—The following publica- tions have recently been issued. Twenty-First ANNUAL Report, Pr. III. 644 pp., 68 pl., 104 figs.—This volume contains papers on general geology, ore deposits and the Philippines. Professor Hosss’s report on the Newark System of Pomperaug Valley, Conn. (reviewed in this Journal, vol. xiii, p. 70), occupies pp. 19-160. ‘The Laccoliths of the Black Hills” by Professor Jacear (pp. 163-303) is a description of the interesting intrusions of rhyolite and phonolite in western South Dakota and eastern Wyoming. The laccoliths are so numerous and the amount of erosion so varied that all parts of atypical intrusion—conduit, basement contact, wedge, flank, crest—are exposed in different parts of the region. These intrusions are assigned to the Eocene and are an effect, not the cause, of the great fractures and dome uplift of the Black Hills. “The fractures reached downward to a zone where molten rock was under pressure. The liquid shot upward into every ramifi- cation of the fracture system.” Ernest Howe has made an extremely interesting series of laboratory investigations (pp. 291-303) imitating the processes of laccolith intrusion and con- sequent deformation of the invaded beds. Professor Van HiszE contributes a paper (pp. 313-434) on the “Iron Deposits of the Lake Superior Region” in which both the geologic and economic aspects of the area are discussed. The Arkansas Bauxite and the Tennessee white Phosphate deposits are described by C. W. Hayes, pp. 435-487. “The Report on the Geology of the Phil- ippine Islands” (pp. 493-625) is by G. F. Becker. It contains general descriptions of the rock types and formations, the min- eral resources, a bibliography and a paper by K. Martin on Ter- tiary fossils. TweEntTy-First ANNUAL Report, Pr. IV. 741 pp., 156 pl., 329 figs. Hyprocrapuy ; by F. H. Newetr, Hydrographer in charge. The tabulation and interpretation of stream measure- ments for 1899 has added much data which is essential if intelli- gent use is to be made of the water resources of the country. Work has been carried on in all parts of the country, and the descriptions (pp. 45-488) are so given as to render the facts directly useful to interested people. A special paper on the Geology and Water Resources of the Black Hills region (pp. 489- 599) is written by N. H. Darron. (Reviewed in this Journal, vol. xiii, p. 68.) “The High Plains and their Utilization,” by Wiarp D. Jounson (pp. 609-741) is an interesting study of the topography, climate and history of the region including parts of Texas, Kansas, Nebraska, New Mexico, and Colorado. The causes of agricultural failure and the conditions necessary to suc- cess are discussed in the light of recently acquired knowledge of soil character, streams and underground water. MonocrarH XLI.—Glacial Formations and Drainage features 390 Scientific Lntelligence. of the Erie and Ohio basins; by Frank Leveretr. (Held for review.) Buuuetins. No. 179.—Bibliography and Catalogue of the Fos- sil Vertebrata of North America ; by OxriveR Perry Hay. Pp. 1-868. Washington, 1902.—The author has rendered an immense service to his fellow paleontologists in completing this list of all the fossil vertebrates described, up to the end of 1900, from all that part of the North American continent lying north of Mexico. The list of systematic names recorded reaches nearly 10,000 ; and the number of titles referred to in the bibliography is about 4600. The author estimates that there are over 40,000 citations recorded. The method of arrangement of the statistics and the mode of citations have greatly condensed the mass of material. The specific names are arranged according to their syste- matic order in the catalogue. A separate key is given of this catalogue, and under each scientific name in the catalogue are given all the citations recorded, but abbreviated to author’s name, date, and a letter (A, B, C, etc.) standing for the separate papers of each author published during one year. In the Bibliography these letters mark the several papers whose titles are given in full. By this means the size of the volume is greatly reduced without omitting the important details called for by the user. A complete index of all the systematic names cited occupies the last 72 pages. The author deserves the gratitude of all paleon- tologists who may use this model catalogue of fossil vertebrates. H. 8. W. No, 182.—A report on the Economic Geology of the Silverton Quadrangle, Colorado; by F. L. Ransome. 258 pp., 16 pls., 23 figs. This is a complete and detailed report on the economic geology, of the ore deposits and mining operations of a quad- rangle situated in the midst of the San Juan Mountains in south- western Colorado. The first part of the report consists of a general description and discussion of the ore deposits and includes a chapter on the general geology of the region by Whitman Cross, while the second part consists of detailed description of special areas and individual mines. The area is covered with a complex of volcanic rocks consisting of a thick series of tufts, agglomerates and lava flows. The ores occur in these rocks ; either as lodes or as nearly vertical stocks of almost solid ore. The chief ore minerals carrying silver are galena, tetrahedrite, enargite, stromeyerite, bornite and chalcopyrite. Gold is present in the ore as native gold almost entirely, no important occur- rences of tellurides being known. The ores were deposited from acid solutions for the most part in preéxisting openings and some of the deposits show the effects of descending surface waters in the secondary enrichment of their upper portions. Ww. E. F. No. 188.—Bibliography of North American Geology, Paleon- tology, Petrology and Mineralogy for 1892-1900 inclusive ; by F. B. Weeks, 717 pp. This bulletin is a combination of bulletins Nos. 130, 135, 146, 149, 156, 162, 172 with the bibliography of Geology and Mineralogy. 391 the literature for 1900. The index (bulletin 189) is to be used in connection with this bibliography. No. 189.—Index to North American Geology, Paleontology, Petrology and Mineralogy for 1892-1900 inclusive; by F WEEKS. 337 pp. The indexes contained in bulletins Nos. 130, 135, 146, 149, 156, 162, 172 are here combined. See above No. 188. ies 190.—A Gazetteer of Texas; by Henry GANNETT. 162 PP. Mr. Gannett ae a brief description of the topography, climate, character of the population, ete. No. 191.—North American Geologic Formation Names : bibli- ography, synonymy, and distribution; by F. B. Wrexs. 448 pp-—This volume is a valuable addition to the scientific registers of facts grown too bulky for memory. The author does not claim that every name that should appear in such a list is actually needed, but every name reported in a list of some five hundred official and serial publications which are given is mentioned. The author has made the list of special value to investigators by presenting the facts exactly as they were presented by the author of the name; thus throwing upon the user of the register the decision as to which name is entitled to first consideration as the proper name of any particular formation. When it is stated that the bulletin contains 448 pages, the indispensable nature of such a register, for the avoidance of further duplication of names, is apparent. We are pleased to see also that it is proposed to con- tinue this list in the annual Bibliography and Index of North American Geology, which has become a feature of the Bulletins of the United States Geological Survey. H. S. W. No. 192.—A Gazetteer of Cuba ;.by HENRY GANNETT. 113 pp. No. 193.—Geological Relations and Distribution of Platinum and associated metals; by J. F. Kemp. 91 pp., 6 pls., 9 figs. No. 194.—Northwest Boundary of Texas ; by Marcus Baker. 50 pp., 1 pl., 5 figs.—An account of the surveys of western Texas from 1859 to 1900 is given and the present status of the boundary is discussed. ‘Our knowledge of the location of the west boundary of the panhandle is very imperfect,” and Mr. Baker advises re-mapping the area. Water Supply AND IRRIGATION PAPERS Nos. 57 (ALABAMA— Montana) AND 61 (NEeBRASKA-—W yomineG).—Preliminary List of Deep Borings in the United States; by N. H. Dartron.—A list of wells over 400 feet in depth has been compiled for each State —arranged alphabetically and accompanied by references to the literature. 2. Lowa Geological Survey ; by SamuEt Carvin, State Geol- ogist. Vol. xii, Annual Report 1901, with accompanying papers. —Detailed geologic maps have been completed for fifty-three counties in Iowa, seven counties having been surveyed during poor: Uhe report on the Mineral Production in Iowa for the year (by S. W. Beyer) shows a substantial increase in coal and gyp- sum, but a decided falling off in the production of zinc. The Am. Jour. Sci1.—FourtH SERIES, VoL. XIV, No. 83.—NOVEMBER, 1902. 27 ~ 392 Scientific Intelligence. Geology of Webster County, by Frank A, Wilder, contains (pp. 138-224) an exhaustive study of the lowa gypsum deposits, as well as those of other American and of foreign localities. The Geology of Henry County is written by T. E. Savage. Cherokee and Buena Vista Counties have been mapped by Thomas H. | Macbride, who presents new facts regarding the limit of the Wisconsin drift and its effect on topography. The Geology of Jefferson County is by J. A. Udden, and that. of Wapello by A. G. Leonard, Assistant State Geologist. Vol. xu is fully up to the high standard of previous volumes of the Iowa survey, espe- cially as regards contributions to stratigraphy and glaciology. 3. The Evolution of the northern part of the Lowlands of Southeastern Missouri ; by C. F. Mansur. University of Mis- souri Studies, vol. i, No. 3, 63 pp., 7 pls.—Southeastern Missouri consists of belts of lowlands enclosing belts and isolated areas of upland. As the result of field study (involving the making of a topographic and a geologic map), Professor Marbut finds the explanation of these belts as follows: The Mississippi River flowed west of (the present) Crowley Ridge, then between Crowley and Benton ridges and finally through Benton Ridge at Grays Point. These successive channels were abandoned in favor of small tributaries of the Ohio; “the Mississippi has been captured by the Ohio twice in succession.” The author’s former paper on this region (Bos. Soc. Nat’! Hist., vol. xxvi, pp. 478-488) described Crowley Ridge as a cuesta, and this erroneous interpretation shows clearly the uncertain character of conclusions based on map study unaccompanied by field work. As Professor Marbut says: ‘‘T’o have determined the whole suc- cession of events and the processes operating to produce them, would have been probably impossible by the methods of library study alone” (p. 39). 4. Geology of the Potomac Group of the Middle Atlantic Slope; by W. B. Cuarxk and A. Brszpins. Bull. Geol. Soc. Am., vol. xiii, pp. 187-214, 7 pls.—A narrow belt of sand and clays, mostly unconsolidated and often ferruginous, form the basal element of the Atlantic Coastal plain. These sediments—called collectively the Potomac Group—are described in detail as regards their composition, fossil contents and economic importance. The relationship of the beds is given as follows: | Raritan Patapsco § Arundel ( Patuxent Cretaceous Jurassic (?) In regard to the conflicting evidence of paleontology and paleo- botany (see this Journal, vol. ii, p. 433, Dec. 1896), the authors think it essential to suspend final decision until more exhaustive investigations of the faunas and floras has been made throughout the entire Coastal region. | Geology and Mineralogy. 393 5. Pleistocene Geology of Western New York ; by H. L., Fatr- » CHILD. Report of progress for 1900. 20th Ann. Rept. N. Y. State Geologist, pp. 105-139 ; pls. 9-41.—Professor Fairchild has made a special study of the Iroquois shore line between Rich- land and Watertown, and finds that the warping of the Ontario basin has occurred mostly since the extinction of glacial Lake Iroquois, and that “the rate of deformation has been much greater than the present rate.” The territory between Syracuse and Oneida was studied with reference to the higher channels cut by overflow of glacial waters. 6. Michigan Geological Survey ; AtrrEeD C. Lane, State Geologist. Annual Report, 1901, pp. 1-304, figs. 1-7, plates i-xv. —Besides the ordinary reports of progress for the year this vol- ume contains a paper by B. E. Livingston on the Distribution of Plant Societies of Kent County, on the lines introduced by Dr. H. C. Cowles. Mr. F. B. Taylor presents an excellent graphic representation of the nature and distribution of surface deposits of Lapeer County (Plate VI). A detailed analysis of the local faunules of the Traverse (Devonian) formation of the northern part of the State is given by A. W. Grabau : the State Geologist _ publishes a geological map (scale 1 in.= 56 miles) revised up to 1902: an illustrated paper on Wave Cutting on the west shore of Lake Huron is contributed by C. H. Gordon. H. S. W. 7. On Vertebrates of the Mid-Cretaceous of the Northwest Territory ; by Henry Farrrietp Ossorn and Lawrence M. LamBe. Geol. Survey of Canada. Robert Bell (acting) Director. Contributions to Canadian Paleontology, vol. iii (quarto). 81 pp., 22 pl. Ottawa, 1902.—Osborn and Lambe have contributed a second part to the quarto memoirs on Canadian fossil vertebrates, begun by the volume on the Cypress Hills species contributed by the late E. D. Cope, in 1891. Professor Osborn contributes the first paper on the Distinctive features of the mid-cretaceous fauna, in which he reaches the conclusion “that the Belly River fauna is more ancient in character both as to the older types of animals which it contains and as to the stages of evolution among ani- mals which are also represented in the Laramie.” (p. 21.) L. M. Lambe contributes the second descriptive paper :—Vew genera and species from the Belly River series (mid-cretaceous), in which are described thirty-four species, of which sixteen are new. H.S. W. 8. Queneau on Size of Grain in Igneous Rocks ;* by ALFRED © C. Lane. (Communicated.)—In this paper (a thesis for the mas- ter’s degree) the author takes up the theory of grain proposed by myself in part 1 of vol. vi of the reports of the Geological Sur- vey of Michigan, and successfully applies the same to the “ Pali- sade” intrusive near New York, and, with very interesting re- * Size of grain in Igneous Rocks in Relation to the Distance from the Cooling Wall, by Augustus L. Queneau. School of Mines Quarterly, January 1902, pp. 181-195, Contributions from the Geological Department of Colum- bia University, vol. ix, No. 80. (This paper was briefly noticed on p. 70.) 394 Scientific Intelligence. sults, to the minette dike of Franklin Furnace, New Jersey. The mathematical foundation has also been worked out for him anew by Prof. Woodward, with accordant results, but whereas I treat the case where the country rock is appreciably heated up, he takes only the case in which the walls of the cooling body are kept at a constant temperature. Unfortunately we have taken different initial temperatures, and otherwise the two methods differ so that the curves and numerical tables cannot be directly compared. The curves of falling temperature given in my paper are referred to the time, whereas in Queneau’s paper the abscissas are laid off proportional to the square root of the time. The early stages of cooling are given, therefore, in more detail, but his remark at the bottom of page 188 as to the slopes of all the curves being equal, is errone- ous. It applies to my curves, but not to his.* Queneau’s results upon the minette of the Franklin Furnace are especially note- worthy; both biotite and apatite vary in size according to the distance from the margin. This shows clearly that these min- erals are mainly not pre-intrusive. Moreover, the size of the apatite increases. clear to the center, while the biotite has a zone of nearly uniform grain occupying nearly the middle two-thirds of the dike. The following inferences of theoretical interest, which, however, Mr. Queneau does not mention, may be drawn: The apatite was formed early, much before the biotite, and probably before the dike had lost even one-tenth of its initial temperature. The dike therefore must have been Jargely viscous when the apatite formed, and the broken condition of the apatite mentioned by Queneau may well be attributed to a strain in the otherwise viscous magma. The biotite was formed later, and supposing, as seems likely from the figure, that the breadth of the zone that has a markedly less grain than that at the center is about one-eighth of the width of the dike, we must infer that it was formed when the dike retained but little more than half its initial excess of tempera- ture. A small dike of diabase, a meter wide, shows in its feldspars that the temperature of its injection was not much above that of the formation of feldspar, at any rate. When he discusses the Palisade trap sheet, however, Mr. Que- neau neglects to. mention that he does not carry his section clear across, nor does he state the thickness of the sheet, nor say * Some other minor mistakes in our papers are: on page 187, one column should be headed x=°85c, and line five above should begin with 95c. I be- lieve there are also some numerical mistakes in the body of the tables. The last column of the table on page 188 is erroneous, for instance. Also on page 191 the units for « are not in square but linear millimeters. In my table, when m=7 if g=°92, the entry should be 74265, and if q is ‘91 the entry should be *73000. In my equation 11 an n has crept in that does not belong there, and on page 117, line 2, for (w) read (2w). Also, in the plate, the decimal point for the horizontal unit is wrongly placed,—it should be log = —01. Geology and Mineralogy. 395 whether he continued the section until the grain appears uni- form. From Kiimmel’s report for the New Jersey Geological Survey, 1897, p. 62, we learn that at one of the points—Fort Lee—the sheet is 950 feet thick, of which Quenean’s section cov- ered only about 100 feet. Of the grain, Ktimmel says that while on the whole the trap is coarse-grained, near the contact it is fine-grained or occasionally slightly glassy, but this rapidly in- creases in size within a few feet of this shale, where coarsest tin tabular crystals of feldspar occur, two or three-eighths of an inch in diameter. The King’s Point trap near Weehawken he estimates from 700 to 875 feet thick, and again Queneau can only cover the margin of varying grain (3449, or 105 feet). From his plates and figures it appears that, so far as he meas- ured, the feldspars still steadily and uniformly increase in size, but the rate of increase of the King’s Point augite drops deci- dedly between 23 and 34 meters. Thus the breadth of the zone of augite which was formed before the center cooled is not far from 100 feet, or about one-eighth of the total breadth. This would imply that the consolidation of the augite took place un- der conditions of temperature, etc., a little nearer those of the initial magma than those of the country rock, and that the feld- spar was earlier formed. We may also infer from his equations of grain (as shown by investigations of mine as yet unpublished) that there is a contact zone of noticeable thickness in which the temperature-was appreciably increased, and that while his data are consistent with Kiimmel’s observations, the grain of the augite at the center is not more than 5™™, being probably about 3™™—q result which it would be interesting to verify. Had we the thickness noted, and that of the contact zone if convenient, and a section representing the central belt, we could have a check on the theory, as well as on the accuracy of the observations ; for the estimation of the grain is a difficult matter, and I doubt if an accuracy of 10 per cent can be obtained, though the diver- gence of Queneau’s observations from his curves is no fair test, for he has done himself injustice, since the curve of linear grain of a great intrusive sheet with a contact zone, like the Palisades, ought not theoretically to be a straight line, but is enclosed by three straight lines as external tangents, which it will usually follow very closely, having only short easement curves near the points of tangency. Queneau’s statement that the zone of varying grain will vary inversely as the temperature of the country rock, is not mathe- matically accurate, and is probably intended merely as a reword- ing of what I say on page 111, that the hotter the country rock the less pronounced will be the zone of finer grain. But I may say that if we have the curve of grain located well enough to determine the three tangents just mentioned, we may infer the ratio of the temperatures of injection and consolidation, the thickness of the intruded sheet and the breadth of the contact zone appreciably affected, as well as a constant involving the 396 Scientific Intelligence. diffusivity of the rock and the tendency of the particular mineral to crystallize. So that we may often give a shrewd guess at the size of the sheet from observations on the grain only at one side. I hope to take up this matter soon. Geological Survey of Michigan, Lansing, Mich. 9. Les Roches alcalines caractérisant la Province petrograph- ique d’ Ampasindava; by A. Lacroix. (Nouv. Archives du muséum d’ histoire naturelle. 4th Ser., Tome I, pp. 152, pl. 10, 4°, Paris 1902, Fascicule I.)—This work is based chiefly on speci- mens and observations collected by M. Villiaume, a colonial official. It is divided into three parts, the first being a descerip- tion of the geology and rocks of Nosy Komba, an island off the northwest coast of Madagascar between the island of Nosy Be and the bay of Ampasindava.* In this portion are described gabbros, nepheline syenites of various types, including dark basic varieties passing into the essexites, ‘They are accompanied by acidic dike rocks, and there is described, in addition, the phe- nomena of the contact of these intrusive masses, both exomorphic and endomorphic. The second part relates to the occurrence and petrography of igneous rocks from portions of the mainland in this part of Madagascar and from Nosy Be. In this are described granites with soda amphiboles, pulaskite, nordmarkite and laur- vikite types of syenites, essexites, quartz bostonites, camptonites, phonolites, trachytes, monchiquites, ijolite, tinguaite, etc., ete. The petrography of these rocks is given with the care and de- tail for which the author’s works are so well known. A number of analyses enhances the value of the memoir, which adds greatly to our knowledge of this little known region. The appearance of Fascicule II, containing chapter ili, giving the general con- clusions and resumé, will be awaited with interest by petrog- raphers. L, Vii. 10. Ueber mariupolit, ein extremes Gilied der EHlaeolithsyenite ; von J. Morozewrcz (Tscher. Min. u. Petro. Mitt. Band xxi, s. 238, 1902).—On the north coast of the sea of Azov in Russia lies an area of crystalline rocks which is being investigated by the author. In the district of Mariupol a portion of this area, between gneiss and granite and comprising about 10-12 square kilometers, has been found to consist of eleolite syenite and pyrox- enite. The investigation of this former rock shows it to consist of 73 per cent albite, 14 per cent of nephelite, 7°6 per cent of aegirite, 4 per cent lepidomelane and 1°6 per cent zircon. The mass analysis gave the following results : SiOz ZrO. Al,Os; Fe2.0; FeO MnO MgO CaO K.O Na.O H,O Sum. 62°53 1:08 18°72 38:26 0°34 0:16 0°08 0:54 0-79 11°77 0°68 = 99-95 In this the relation K,0: Na,O::1:24. The texture is variable, sometimes coarse, sometimes fine, and sometimes porphyritic. The feldspathic components are set through with aegirite needles. * (Stieler’s Hand Atlas gives Ampassandava. ) Geology and Mineralogy. 397 Separate analyses of the mineral components are also given. To this rock of the syenite family composed almost solely of soda- bearing constituents, the author gives the name of Mariupolite. L. Vieibe 11. Dahamit, ein neues Ganggestein aus der Gefolgschaft des Alkaligranit ; von A. Prexixan. (Denkschriften der mat.-nat. wiss. classe der K. Akad. der. Wiss. Wien, 1902. Bd. lxxi.)—In an article dealing with the petrography of a rock collection from the islands of Socotra, Abd el Kuri and Semha the author de- scribes a dike rock of a chocolate brown color, compact texture, containing red phenocrysts of thin tabular feldspar. The micro- scopic study and the chemical analysis shows the rock to consist of 6°8 per cent riebeckite, 43°8 per cent albite, 2°8 per cent anorthite, 12°2 orthoclase, 31°5 per cent quartz. The chemical analysis by E. Ludwig gave $i0, Al,0, FeO; FeO MgO CaO Na,O K.O H,O Sum. 74:02 13:56 1:93 1:09 0:28 0:56 5°80 2°06 1:05 = 100-30 The phenocrysts are albite or albite:oligoclase, containing the small amount of anorthite. The other components are mixed in the groundmass. ‘The author suggests the name from the locality, Dahamis, and offers the fact that it differs from grorudite (quartz tinguaite) in containing riebeckite instead of aegirite, as a reason for the new name. He overlooks entirely, however, the fact that Osann (Tscher. Min. Mitt., vol 15, p. 485, 1895) has already described a dike rock consisting of alkali feldspars, quartz and riebeckite under the name of paisanite, the analysis of ‘which also agrees in essential particulars with that above. The rock should be regarded as a variety of paisanite. Be Vuk: 12. Mineral Resources of South Dakota ; by C. C. O’Harra | and J. E. Topp. South Dakota Geol. Survey Bull. No. 3, pp. 130; pl. 31.—The mineral wealth of the Black Hills has already been described by Professor O’Harra (this Journal, vol. xiii, p. 474). Professor Todd, State Geologist, gives a report (pp. 81- 130) on the mineral Building Materials, Fuels and Waters of South Dakota. 13. Note on anew occurrence of Native Arsenic; by NEvit Norton Evans. (Communicated.)—During the past summer native arsenic was discovered in a calcite vein cutting the nephe- line syenite at Montreal, Canada, by Mr. Edward Ardley, Museum Assistant at the Peter Redpath Museum, McGill University. The mineral appears to be pure arsenic, not more than traces of other elements having as yet been found in it. The vein has a maxi- mum thickness, so far as has been seen, of two inches, and has already yielded about fifty pounds of the arsenic. A complete analysis, together with a detailed study of the occurrence, is being made by the writer, and will be published shortly. McGill University, Montreal. 14. The Inverness Earthquake of September 18th, 1901, and the Carlisle Earthquake of July, 1901; by C. Davison. Quart. 398 Scientific Intelligence. Jour. Geol. Soc., vol. lviii, pp. 371-397, 2 pls.—The recent Inver- ness earthquake gives additional proof of the existence of a fault line reaching from Loch Ness to the sea and this region “ appears to be in a stage of more rapid development than any other in the British Islands” (p. 396). The earthquakes of 1816-18, 1888, 1890, and 1900 were along the same fault. The Carlisle earthquake has led to the recognition of a deep- seated fault (running N. 5° E ) in a region where there is no sur- face sign of such a structure. MISCELLANEOUS SCIENTIFIC INTELLIGENCE. 1. Beitrdge zur chemischen Physiologie und Pathologie, her- ausgegeben von FRanz Hormeister. II Band. 1902 (Braun- schweig, F. Vieweg und Sohn. 15 M.).—This completed volume, of which the earlier numbers have already been reviewed in this ~ Journal, brings evidence of the same high standard which char- acterized the first one. The Beitriage have now won a place in the permanent literature of physiological chemistry. Particular attention may be directed to the recent contributions on the products of proteolytic digestion and the studies on various pro- teids of animal and vegetable origin. L. B. M. 2. Les Dirigibles ; by M. H. Anpr&. Pp. ii+346. Paris: Ch. Béranger, editeur. 1902.—This is a well arranged and use- ful hand-book of the theory and practice of aerial navigation as — it is known at present. As indicated by the title, the larger part of the book is occupied with dirigible balloons, and much inter- esting and valuable information “has been collected upon the various conditions of this difficult problem ; the laws of the resist- ance of the air, so far as they are known, are applied to the determination of the proper shape and dimensions of the balloon itself, of the propellers, rudders, etc., and some consideration is given to the motors which may be employed ; the very important question of stability also receives attention. The book concludes with a critical account of the various experiments which have been made with dirigible balloons from the celebrated attempts of Gifford in 1852 and 1855 to the recent achievements of Santos- Dumont. H. A. B. 38. An Introduction to Physical Geography ; by GrovE Kar. GitpeERT and ALBerT Perry Bricuam. D. Appleton & Co. 370 pages, 263 illustrations.—Gilbert and Brigham’s Physical Geography is thoroughly scientific, up to date and attractive. It is a good introduction to out-of- door science of any sort. 3 ff | Am. Jour. Sci., Vol. XIV, 1902. Plate IX. Fic. 1.—BOWLDER TRAIN UPON THE SLOPE OF SHERMAN HILL The view looks north-northwest along the train toward the crown of the hill. wo Fic. 2.—SouTHERN END OF THE TRAIN OF BasaLT BLOCKS FROM SHERMAN HILL. The view looks north-northwest along the train, Sherman Hill itself, distant a mile and a half, appearing between the two largest blocks. THE AMERICAN JOURNAL OF SCIENCE [FOURTH SERIES.}] Art. XXX VII.—An Instance of the Action of the Ice-sheet upon Slender Projecting Lock Masses ;* by WILLIAM HERBERT Hopss. (With Plate IX.) THE present paper will discuss what seems clearly to be a case of degradational action by the ice mantle exerting its pressure in a lateral direction against steep and slender masses of projecting rock. The conditions are in some respects pecu- liar to the locality, which lies in an island-like area of Newark traps and arkoses within protecting walls of the crystalline schists—the Pomperaug Valley area of Connecticut. The pre- servation here of the Newark rocks from erosion, which has elsewhere so generally removed them, is a direct result of their deformation by jointing and their depression in the form of a composite crustal block along the marginal joint planes as fault walls.t This depression has been irregular in so far as the blocks of the smaller orders of magnitude within the larger composite block have been depressed by different amounts so as to produce a mosaic of small prismatic blocks. The present positions of basalt and arkose within the area are also dependent upon the high position of the main basalt flow in the local Newark series, and upon the low easterly dip (420°) of the beds and flows previous to their dislocation. Their positions are further affected by the fact that the displacement by fault- ing was distributive largely within a marginal zone. As a result of all these conditions the dense resistant basalt now occupies the central portion of the depressed area and is bor- dered by the softer shales and arkoses. Could the area have been visited subsequent to its deforma- tion by faulting but previous to its degradation through the * Read before the Wisconsin Academy of Sciences, Arts, and Letters, at Milwaukee, December, 1901. +The Newark System of the Pomperaug Valley. 2ist Ann. Rept. U.S. Geol. Survey, Pt. III, pp. 1-160. Am. Jour. Scl.—FourTH SERIES, Vou. XIV, No. 84.—DEcEMBER, 1902. 400 W. Hf. Hobbs—Instance of the Action of the agencies of subzerial and of ice erosion, we may believe that it would have presented an irregular surface not unlike that of a mosaic from which a local area of the back had become dis- placed and the overlying blocks allowed to slide down by small amounts while still restrained by their friction upon their neighbors. The effect of subzerial erosion has been to etch out the marginal areas of soft sandstone and leave the basalt prisms of the central area in strong relief like the image of a cameo. The basalt itself discloses no marks of the suberial erosion, for the reasons: first, that it is intensely resistant; and, second, that its area is so small (six miles in length by two miles in greatest breadth) that no streams of any power have been developed upon it. It is not, however, to be assumed that no considerable degradational action has occurred within the area of the basalt masses of the valley, for the three upper members of the Newark series found in the Connecticut Val- ley area, which begins less than a score of miles to the east, are missing from the Pomperaug Valley series, and were doubtless removed by subeerial erosion, while large thicknesses of the surrounding schists were being carried away. Fic. 1. Schematic profile of basalt ridges of the Pomperaug Valley. Black, basalt; black spotted with white, amygdaloidal basalt ; white, shale ; white with black circles, conglomerate (where stippled, baked zone of con- tact) ; stippled area, drift and alluvium. The work of the ice within the valley is revealed in the pro- files of the basalt ridges. These ridges have generally fault scarps on their western and northern sides (which face in the direction from which the ice moved) and gentle slopes to the eastward and southward, conforming to the dip of the beds and flows of which they are composed. In these general outlines the action of the ice is not disclosed, but the caps of all the ridges seem to have been removed by an appreciable fraction of their height. This is brought out in the schematic figure 1 and in the author’s report above cited.* That this degrada- tional action by the ice is localized largely at the crests of ridges is also shown by the texture of the rock found at the crests when compared with that upon the flanks of the southern ridges. Dense and massive at the crest in correspondence with the lower beds of the flow, it is amygdaloidal and vesicu- lar upon the southeastern flanks, where it doubtless represents upper layers of the flow. * Loe. eit.; pl. Ves A. Ice-sheet upon Slender Projecting Rock Masses. 401 Some clue to the manner of decapitation of the basalt ridges may be found in two trains of basalt blocks, one of which is represented in Plate IX. This train, which is the one of the greater interest, proceeds from the ridge known as Sherman Huill,* the extreme southwestern elevation of the 2 g ty ® en KEY PE Ke Fic. 2. Sketch map of the Pomperaug Valley showing the distribution of the terrace deposits and of basalt trains. W., Woodbury; S., Southbury ; S. B., South Britain; W.O., White H., Hotchkissville; P.. Pomperaug ; Oaks; S. H., Sherman Hill; R. H., Rattlesnake Hill; C. R., Castle Rock. The stippled area represents roughly the distribution of the terrace deposits, and the lines of larger spots the trains of basalt blocks; A., area of terrace excavated for railroad fill. * Sometimes considered a part of Rattlesnake Hill. 4.02 W. H. Hobbs—Instance of the Action of the basalt within the valley. _The position and direction of this train is brought out in fig. 2, which is a sketch map of the Pomperaug Valley. Upon the south-southeastern flank of Sherman Hill the train begins as a collection of irregular blocks of basalt, occupying a belt about one hundred feet in width and extending from the present low tower-like crest of the hill to the corner of the highway, where is the edge of the terrace floor of the valley and where the train appears to end abruptly. Within this portion of the train are a dozen or more blocks six to eight feet in diameter, and very many smaller ones. Fig. 1, Pl. LX is a view looking up the train from a point near the road corner toward the summit of Sher- man Hill. Lost in the terrace deposits of the valley the train is again picked up upon the south side of the valley so soon as the slope begins to rise above the level of the terrace. This local- ity is near and west of the road from South Britain over Georges Hill (see fig. 2) and just above the great fill upon the railroad. The sand and gravel for this fill was obtained from the area immediately north where indicated upon the map (A of fig. 2). Mr. Henry M. Campbell of South Britain — pointed ont to the writer a place where three large blocks of the basalt, one of them six feet or more in diameter, were unearthed and removed by blasting during the excavation of this section of terrace. The location would fall within the line of the train from Sherman Hill. The blocks now in evidence south of the railroad fill are of special interest because of their location in the line of the train and because of their unusual size. Fig. 2, Pl. LX, which looks northwestward along the train, includes two of the largest. The hill from which they were separated is visible in the dis- tance (more than a mile and a half away) between their tops. There are several blocks of this size (15 to 25 ft. in largest dimensions), some partially buried in earth along with many smaller blocks, but all located within a belt less than a hun- dred feet in width. The train does not appear to extend south- ward beyond this point, but no attempt has been made to follow it farther. The direction from Sherman Hill of these great blocks of basalt, which form a landmark in the valley, is S. 28° to 29° E., a value near that of the average movement of the ice over the higher points in the vicinity. The conditions seem here to be best explained by assuming that from the pre-glacial surface produced by subeerial erosion the faulted prisms of basalt projected in pinnacles above the softer sandstones, in part opposing to the ice stout walls and in part comparatively slender walls and towers. Sherman Hill, as indicated by the geological map in the report here cited, Ice-sheet upon Slender Projecting Rock Masses. 4038 unlike practically all of the other ridges of the valley, opposed its long face and, therefore, its weakest direction to the ice mass, which was directed against its thin vertical walls. Owing in part to dip and in part tothe manner of faulting, its western end (the present peak) projected above its general wall-like mass. This part also was unprotected by the higher mass of Rattlesnake Hill. In this way, it is believed, the great blocks which are now found over a mile and a half away and con- nected by the train with this elevation were separated from their parent mass. Castle Rock, a prismatic block of nearly equal basal dimen- sions and now having a sheer cliff upon its northern face nearly one hundred feet in height, is located in the north- eastern part of the area.* Like the west end of Sherman Hill its position left it unprotected by other masses from the north- west, where a considerable valley allowed the ice to sag well below the crests of the elevations surrounding the valley. The row of basalt blocks located southeast of White Oaks is believed to have been derived from this elevation much as the other train has been from Sherman Hill. The slender nature of the prism of Castle Rock, its considerable elevation above the general level, and its exposure upon the northwestern edge of the area all favor such an hypothesis. The direction of this train (S. 13° E.) would indicate that the long valley east of the basalt masses has modified the direction of movement of the lower portions of the ice mantle. That the ice found a depression in the Pomperaug Valley, into which its substance sagged, is indicated by the present altitudes of the higher basalt ridges which have been decapi- tated, in comparison with those of the gneiss hills of the vicin- ity (the basalt ridges are some 200 to 300 feet the lower). It must be assumed that erosion in post-glacial time has been more effective upon the gneiss than upon the basalt, though this would doubtless be modified by the soft arkose members above the main basalt. To ascribe these trains to the separation of blocks from the lee side of ledges due to the frictional action of overriding, is to leave unexplained their large size and the distance to which some have been carried, more especially, however, the restric- tion of the trains to ledges which the geological study shows to have been slender in form and with deep valleys northwest of them into which the ice could sink and act in a horizontal direction against their walls. Professor Chamberlin has informed me that he has observed in Greenland an undoubted instance of such degradational action of the ice from lateral pressure upon rock walls. University of Wisconsin, Madison, Wisconsin. Soe. cit, fie: 42, pe bit, 404 Koenig—New Species Melanochaleite and Keweenawite. Art. XXXVIII.—On the New Species Melanochalcite and Keweenawite. With Notes on some other known species ; by GEorGE A. KOENIG. 1. Melanechaleite. For the material of this investigation 1 am indebted to Captain James Hoatson, of Calumet. I received it early in January of 1902, and informed that gentleman—about January 17th—that I had much reason to distinguish the black mineral as a new mineral species, for which I proposed the name melanochalcite (from pwédas and yadxes). Occurrence.—The material comes from the exploration shaft of the Calumet and Arizona Copper Mining Company, near Bisbee, Arizona. I am informed by Captain Hoatson that these specimens represent the character of the ore at a depth © of 800 feet. All the mines in that district exhibit oxidized ores to a very considerable depth. Sulphides are rare. I had examined and assayed a number of samples for Captain Hoat- son from time to time as the sinking of the shaft proceeded; all oxide ores, and of exceptional richness. Nosamples assayed under 10 per cent copper. Cuprite was always preponderating, sometimes mixed with much hematite; say, for instance, 30 per cent of the former to 70 percent of the latter, as an extreme. Malachite and chrysocolla appeared sparingly ; noazurite; whilst at the Copper Queen Mine, of the same belt, the silicate and the carbonates are in the foreground. The material under consid- eration in this paper differs from that of the upper shaft. The material before me presents hard spheroidal nodules, cemented together by a soft, brown-red, clayey material, easily removable. The nodules’ nucleus is formed by granular cuprite, with occasional druses, the latter lined with octa- hedral crystals. This kernel is surrounded by a zone of pitchy-black mineral, a few millimeters in thickness. Upon this follows a banded green zone of chrysocolla and malachite. Thereupon follows white, or transparent, quartz. Within the quartz are smaller cuprite kernels, each with its aureole of black and green. Here the black material is thicker, but less pure asa whole. The purest substance is always thin, lying close to the cuprite. It passes into deep olive green; then light olive-green into the pure green of chrysocolla, or mala- chite. Thus the fracture-surface of a nodule is of striking beauty. The one before me, which served as model for the description, has an average diameter of 120 millimeters. The kernel is not centric, and rather oblong than circular. The black, green and white parts are massed chiefly on one side. Koenig—New Species Melanochaleite and Keweenawite. 405 This material reminded me of the German “ Kupferpecherz,” which has been declared by eminent authorities as a mineral mixture of various bodies—chiefly chrysocolla and limonite. Dana places it under chrysocolla. JI have analyzed such material coming from the Old Dominion Mine, Arizona, of a brown-black color. It was more the esthetic beauty of the present material which induced me to enter into its study, than the expectation of finding new facts. Absence of definite erystalline form is ever apt to call up a prejudice against the homogeneity or chemical integrity of bodies. In the present instance, additional reluctance was caused by thinness of the black zone. But since there was plenty of material, the ques- tion of obtaining a sufficient quantity of satisfactory substance could be answered by care and patience. Physical Examination.—l picked out successively, and from different nodules, three portions of material—A, B, C. The sequence of the letters denotes the degree of scrutiny employed. “A” was intended for preliminary work, “B” for chemical orientation, and ‘‘C” for the final trial. "At the beginning the chief care was the rejection of either red or green particles. But it was quickly discerned that among the dark material there was a lustrous and a dull portion; a banded and a bandless part. High lusterand absence of band-strueture go together; dullness and banding are yoked. Sample “A” was tainted somewhat by red, by green and by dull particles. Sample “B” was only contaminated by dull parts; but “C” was picked over several times, and contained only brilliantly- black material. This was time-consuming. It will be seen, however, from the analyses that the blemishes were rare even in “A” and “Bb.” The black mineral is fairly hard—about 4; but it is exceedingly brittle. The cause of this brittleness lies, probably, in numerous microscopic fissures. As support for this opinion, I mention the long time required for the ceas- ing of air bubbles to rise, when the mineral was placed under water (specific gravity determination). And also the failure to obtain a thin plate by grinding; the plate going to small pieces long before translucence was reached. When the min- eral is eround i in a mortar it shows the disagreeable property of © “smearing.” The fine powder is coffee-brown in color. Some of the finest dust from sample “ C,” which had stuck to the mortar, was brushed upon a glass slide, imbedded in Canada balsam and examined under the microscope. It proved to be translucent, letting through yellow-brown light, one par- ticle exactly as the other. The mineralogic uniformity and singleness of this material (“C”) is undoubtable. In polar- ized light these dust particles behaved like an amorphous, or isotropic, body. The specific gravity was found to be 406 Koenig—New Species Melanochalcite and Keweenawite. — = 4-141 at 21 C. (material “C”). . This number is rather under than above the true weight, because I wished to avoid boiling, in order not to interfere with the water-per- centage of the material. To even up matters, the water used was saturated with air at 21 C. for both weighings. Chemical Hxamination.—B. B. In closed tube the sub- stance looses water and CO, and the coffee-brown powder turns to brown black. With the fluxes only copper reaction, except with microcosmic¢ salt, when a fine skeleton of SiO, appears in a blue glass. The mineral is readily decomposed by HOl of all concentrations, even when in coarse fragments. If such a fragment be placed in 3 per cent HCl, and one observes with a pocket lens, one sees the margins of the splinter turn white. The white zone widens steadily, until nothing but a white mass remains, which occupies the entire space of the original black substance. And yet the percentage of SiO, is not quite 10. While this dissolution is progressing ove sees a steady spray arise of minute bubbles of CO,, very different from the big air bubbles arising from the microscopic capillary fissures. I con- sider this behavior as the essential foundation of my hypothesis regarding the constitution of the molecules of this mineral— to wit: SO, and CO, are simultaneously liberated, whilst CuO and H,O pass into the solution. The resultant SiO, is what I would eall semigelatinous—not colorless and transpar- ent, but white and translucent. It is readily dissolved by the water solution of NaHO. There is no euprous chloride formed. The copper is altogether cupric. Material ‘“‘ A.’—preliminary analysis. Weight of substance taken, 0°5361 gr. | 0:0671 loss by ignition. 00532 SiO, 00010 Fe,O, 0-4188 Cu,S The sulphide was dissolved and electrolyzed, yielding 0°3277 Cu=0°4107 CuO, to which must be added 0:00015 CuO, obtained from the electrolyte by H,S. Total, 0°4122 CuO. | In percentage : 3 Gud. = 76:72 SiO, = 9-91 TGQ) facrerse CO, == Ra? Ke:0.. = 0219 Koenig—New Species Melanochalcite and Keweenawite 407 Material “B.” 0°5658 gr. The tenacity for water at in- creasing temperature was tested by exposing the powder, for two honrs each, at the following temperatures : 0°0092 loss at 88C. 0°0142 va Hoe: 0°0082 s5 160 C. 0°0128 eG 210.C. 0°0444 0°0451 loss at red heat. 0°0895 total loss. CO, was not separately determined in this sample; but from the determinations in “O,” when H,O and CO, are nearly alike, the inference may be drawn that all the water is expelled . at 210 ©. 0°0500 SiO, ; 0°3415 Cu+0-0082 CuO from electrolyte by HS, 0°0008 Fe,0,. CuO = 76°46 SiO, = Soo ORE uae, H,O ( == 4°20 Fe,O, =) 0°14 99°63 Material ““C” — This having been proved irreproachable material, the analysis was made with great care. OO, and water were determined as follows: 0°5260 gr. of the fine powder was placed in a porcelain boat and the latter heated in a combustion tube to redness, whilst a slow current of per- fectly dried and purified air passed through the tube. An “U” calcium chloride tube received the water and a Geissler Potash bulb received the CO,. The increase of weight in the former was 0:0407 gr.; in the latter, 0:0378 gr., a total of 0-0785 gram. At the same time the weight in the boat decreased by 0:0766 gram. Hence there is here an error of 0-0019 gr., which may be evenly distributed between H,O and CO,, or may even be neglected altogether without affecting the result sensibly. The copper was precipitated electrolyti- cally, and in this case H,S found no residue of copper in the electrolyte. The latter being thereupon rendered ammoniacal, a flocculent precipitate fell, which, after filtering and ignition, showed by its color that it did not consist of iron oxide alone. It was found to be ZnO+Fe,O,. I had overlooked the zine in the other analyses. | 408 Koenig—New Species Melanochalcite and Keweenawite. The percentages are: Molecules. CuO, 117688 2 79 =] OESSs SiO, = 780: 60 =0-12914 9 CO, = 7:17:44 = 0°16295 to eager H,O = 771 :18 = 0-42833 ZnO = 0°41 : 81 = 0:00506 BO” = OVE 100-04 This unusual, and surely novel composition, may give cause for several inter pretations. Roughly speaking, it might be an intimate mixture of copper carbonate, copper silicate and copper hydrate; but it may also be interpreted as the basic salt of an ortho-silico-carbonie acid H,(Si,C)O,, in which Si and C may replace each other within certain limits. A scrutiny of the three analyses shows a practically identical percentage of copper oxide. The percentages of SiO, and of the volatiles vary. As to SiO,, we have 9-91 (“A”); S8ai("ai ee (“C”), a variation of about 1 per cent. In “A” we have 12°52 volatiles; in “ B,” 14:2; in “C,” 14°88. These figures are evidently not due to accident, nor due to mechanical mix- ture. Unfortunately their significance was recognized only after it was too late for a determination of CO, in “A” and ““B,” for there was nothing, or too little, of the materials left. Notwithstanding this serious experimental deficiency, it seems to me that the logical comparison forces the admission of strength in my hypothesis. Admitted the existence of a com- plex H,(Si, C)O,.H,O (and I can see no chemical reasons against it) in which hydrogen is wholly replaced by Cu, and H,O partly by CuO and in which, moreover, Si and C are atomically interchangeable: but so that the percentage of Ou be constant, then a change in the percentage of Si,0, must influence both the percentages of CO, and H,O. Now, com- paring “A” and “C,” we find in the former 2°11 SiO, more, and 2°35 volatiles less than in the latter. 2°11 SiO, are equiv- alent to 1°53 CO,, leaving 0°82 as that portion of the volatiles attributable to water, thus conforming with the hypothesis. If the composition of melanochalcite be interpreted accord- ing to this plausible hypothesis, the figures of analysis “C” take the following shape. Molecules Si,O, = 0°12914 CO. 220° 16295 0°29209 These 0°29209 molecules require 2x 0°29209=0°58418 mole- ecules of CuO. Koenig—New Species Melanochalecite and Keweenawite. 409 - There are disposable 0°96583 CuO+0-00506 ZnO, a total of 0-97089 molecules of basic oxides. Deducting from this total the requirements of the silico-carbonate, there will be left 0-97089—0°58418 = 0°38671 (CuO,ZnO} to constitute with the water, the hydroxide. But we have 042833 molecules of water ; hence there is a surplus of the latter of 0°42833—0°38671= 0°03762. This surplus, which amounts to 0-749 per cent, must be declared present as hygroscopic water. It is not determin- able by experiment, since the substance lost at 87 C.—1°63 per cent, and since it is a well-known fact that boilmg water converts the hydroxide Cu(HO), into the oxide CuO. Putting together these figures, we get : Copper silico-carbonate 0°87627 : copper hydroxide 0°77342 = 1°000: 0°882. The formula of melanochalcite is: Cu,(Si,C)O, - Cu(HO), Paragenesis.—In regard to the forming of this mineral sub- stance, one may conceive of at least two modes : (1). Cuprite crystallizes first from a solution of copper ear- bonate, with the codperation of a deoxidizing agent, and pro- duces centers or nuclei. At a later period an oxygenated aqueous solution of silicon and carbon meta-acids invests these nuclei. In presence of an overwhelming basic substratum, the meta condition of the acid changes into the ortho state, and the melanochalcite molecules are formed rapidly, falling out in amorphous aggregates. As the crust increases in thickness the basic substratuim’s influence decreases and we find mixtures of melanochalcite aggregates with those of chrysocolla and malachite, because the ortho reverts to the meta state. The complex molecule Cu,(Si,C)O, is no longer possible; and, shortly after, we have clear alternating bands of chrysocolla and malachite. (2). One can conceive of an aqueous solution holding from the start all the constituents, excepting only oxygen, and from which the least soluble constituents, eee CUTS), will fall out first. But considering the great bulk of the latter compared with that of melanochalcite, chrysocolla and malachite, this view would seem less simple than at first. Both are purely hypothetical ; no experimental facts are known to me outside of the formation of copper sulphides and arsenides. A large field of investigation is open here. The relative absence of native copper in these Arizona cuprite ores is surprising, because these ores are evidently neither metamorphic nor pseudomorphic ; but appear to be automorphic, the same as the native cope ores of Lake Superior. 410 Koenig—New Species Melanochaleite and Keweenawite. 2, Heweenawite. Occurrence.—In April 1901, driving the fifth level at the Mohawk Mine, Keweenaw Co., Michigan, southwestward from shaft No. 1 to shaft No. 2, a narrow cross vein was cut through, carrying domeykite and a reddish-metallic mineral having the color and general appearance of massive niccolite. Superin- tendent Fred A. Smith sent me some of the material. Being very busy at the time, I did not investigate this matter until June, after my vacation had begun. The examination revealed then my wrong, first impression, inasmuch as the substance showed copper, nickel, arsenic in the ratio of 2:1. Early in July I visited the mine and informed Superintendent Smith that I proposed the name Aeweenawite for this undoubtedly new mineral species. I went under ground for the purpose of gaining some knowledge of the paragenesis of the arsenides for which this mine has now become famous. The large domey- kite-emohawkite vein crosses the amygdaloid copper-bearing bed near the No. 1 shaft at an angle of nearly 45°. The arsenides in large shining masses sit mostly against the reddish amygdaloid, without the intervention of any selvage. There is little parallelism among the several minerals (the least soluble species forming the bordering fringe), which suggests the notion of the fissure having been filled by crystallization from a stand- ing mother liquor. In the absence of parallelism, the mother liquor must have been in motion. The stoping operations on this vein between the second and third levels tend to show the vein as a system of flat lenses. One of them has been stoped out with a rich yield. I found the new ‘vein to be about 1,300 feet from the large one just described, near shaft No. 2. The vein comes into the level very flat, almost parallel with the strike of the bed. It is thin, with a maximum width of 6 inches. The general character is very like that of the large vein; to wit, absence of parallelism. Sometimes calcite sits against the amygdaloid, sometimes quartz, or again either domeykite or keweenawite. The conditions under which the filling out of the vein took place must have been alike in both veins. I intended to analyze a large sample of the amygdaloid adjacent to the vein in order to learn whether the arsenic per- vades the rock in minute quantities, to find proof or disproof of a lateral leaching. Thus far I have not done this, though the intention still exists. This is one of the reasons why I kept back the publication of the present notice. Physical Properties.—I have observed the mineral only as a massive, very fine granular aggregate which is very brittle and shows flat conchoidal fracture. Hardness about 4, similar to that of domeykite. The color on the fresh fracture is pale Koenig—New Species Melanochaleite and Keweenawite. 411 pinkish brown. On exposure tarnishes to a deeper brown red; but is far more constant towards the atmospheroids than domeykite or mohawkite. I have now some specimens before me which have been exposed to the laboratory gases for over a year and still show the characteristic color, but slightly deepened. Specific gravity at 20° C.= 7-681 (with 3:140 grams of the mineral). Chemical Characters.— B. B. melts easily to a globule. Gives vapors of arsenic. On continued blowing in oxidizing flame, a metallic globule is obtained. But if a borax bead be placed along the globule from the first, while the O. F. is act- ing, then a blue glass is obtained ; later a brown glass, and ultimately a green glass, showing successively cobalt, nickel, copper. The qualitative behavior is thus identical with mohawkité. Dissolves in concentrated HNO, and even in HNO, (Specific gravity 1-2). A first preliminary quantitative determination gave Ou= 38°5; (Ni+ Co) = 17°98; quartz = 4°52; no iron—the dif- ference must be arsenic. This was very different from mohawkite. A second analysis of the same sample, carefully made with O, 500 grams, gave 00249 insoluble 0°3760 Mg, As,O, 0-2449 Cu,S | 0:0945 Ni + Co (by hydrogen) 0°0047 Co (by hydrogen). From this follow the percentages. Quartz = 4°98 As — eae 5 a “== 0493 Cu en ae ae = G2 t a = a : 58-6 = o-ag5 (9944 Fe = trace 99°96 Thus the ratio obtains As : (Cu,Ni,Co) = 1,000: 1,915 and again Ou : (Ni+ Co)=2:1 nearly. It was. assumed by me that this ratio between the metals would probably not be constant; but instead to a certain limit a replacement of each by the others, the same as was assumed for the mohawkite and has been fully proven by numerous analyses, I have made since. Keweenawite = (Cu,Ni,Co), As. 412 Koenig—New Species Melanochalcite and Keneenawite. This result was communicated to Superintendent Smith at my visit to the mine on July 6, 1901. The material had come from the sixth level. I collected material at the vein crossing on the fifth level. In appearance it was identical with the one just described. The analysis made with 0°5 gram samples gave the following data: 0°3379 Cu,S 0'0487 Ni 0:0047 Co 0°3560 Mg, As,O, 0°0039 quartz. The percentages are: Cu 53°96 :63 = 0°856 A, — atta ea fe) ~J i 34°18 Aoi oi pees (A Quartz 0°78 99°60 The ratio (Cu,Ni,Co): As = 2:27:1, is not so close to 2:1 as that of the first material, but still sufficiently so. The material, though freer from quartz, was not so faultless through- out as the first. There appeared certain pseudocleavages along which a thin olive-green film could be seen. Just to what extent this condition has to do with preponderance of the ~ metals over the arsenic, [ am not prepared to say. But on the other hand, this analysis shows unmistakably the replacement of copper by nickel, and vice versa. A third analysis was made with another sample, the arsenic not determined. Quartz = 060 Cu == 40°72, 3: 63 (= 06646 ae a se : 58-6 = 0346 ( 999? Fe = trace (diff) As = 88°42 os. Was 0°515 100°00 (Cu, Ni, Co)inats = T1282 4 x In my paper on mohawkite (this Journal, December, 1900) I showed how an arsenide Cu,As forms very easily when the vapors of arsenic act upon copper at red heat. This artificial Cu,As shows the color and crystalline structure of chalcocite. The difference in color in keweenawite must, therefore, be owing to the nickel. Koenig—New Species Melanochaleite and Keweenawite. 413 I give the specific gravity (1. ¢.) as 7°71, the calculated specific gravity as 7°75, whilst the keweenawite gives the gravity 7-681, which is very close indeed. Nickel and cobalt having nearly the same specific gravities and not much different from copper, this slight difference is readily accounted for. 38. Mohawkite and Domeykite. During the past year I have made several more analyses of these two minerals from the Mohawk mine. The material was in part collected by me on the spot or sent to me by Mr. Fred Smith, to whom I wish to express my indebtedness. The colors of these minerals seem alike to those of the fabled chameleon, and the identification by the eye is made very difficult, in fact impossible. a. The mineral appears in form of large masses in calcite with a color equaling that of chalcopyrite; altogether unlike any previously seen domeykite or mohawkite. Mr. Smith - states that it had this yellow color when it came up the shaft.. It is exceedingly brittle, crumbling between fingers into blue and purple fragments. B. B. shows trace of cobalt and trace of antimony. Cu = 70°56 As = 29°50 It is therefore domeykite. 6. Large iron gray mass, looks like arsenopyrite. B. B. gives. strong cobalt reaction. Cu = 67°86 Ni + Co =. 3°32 AS =e nO 99°28 The mineral proves to be mohawkite ; but the sum of cobalt and nickel is only one-third of that in my original mohawkite. c. Mr. Knight, one of my students, picked up a specimen at the Mohawk mine, which seemed to be peculiar. It is tough, but not so much as what I have called mohawk-whitneyite, gray color and fine granular structure somewhat like algodo- nite in appearance. 7 B. B. reaction for antimony, no cobalt, no nickel. Spec. gr. 8°378 — 8°364 (with 1°747 grams) Cut= S02. :. G3 = 1281 Ais == VOT ts ==)0'255 Sb = 0re# 120'=" 0-007 100°68 Cur (Acs, a9 2 eo 414 Koenig—New Species Melanochalecite and Keweenawite. On the face of this result the establishment of a new species would seem indicated. But as I have expressed myself (1. ¢.), the higher ratios of these copper arsenides are either down- right mixtures (grain very fine) or they pertain of the nature of alloys and hence all ratios are possible. In order to throw a little more light on this subject, a long sliver was knocked off the type specimen. On this sliver the mixture of two substances was discernible. The sliver was broken into three fragments and in each the copper was determined. a (0'5063 gram) gives Cu,S = 0°4836 per cent Cu = 76:2 8(0'500 gram) “ So sa OUIASY ps Cu.= 75°76 y (0506 gram) “ cs eS ODS. kn as Cu = 80°10 These differences would seem to bear out my statement. A. straight ratio marks an accident rather than a necessity. In speaking of mixtures like these, it may perhaps be well to use the term mohawk-algodonite, as distinguished from true algodonite. d. Mr. Rogers, another of my students, collected a specimen which did not quite correspond to anything I had seen before. It was much tougher than the preceding specimen. A frag- ment weighing 0391 gram was dissolved and. the copper determined. Arsenic by difference. Nothing insoluble. Cu,S = 0:4208, Cu = 0°3361 = 85°9 As = o= dard : 100°0 Ratio 7°25: 1 It must be classified as mohawk-whitneyitte. e. Genuine Algodonite from the Champion Mine, on the South Copper Range. I am indebted to Dr. L. L. Hubbard, the Superintendent, for the specimen. It presents a piece weighing about 400 grams, through which a drill-hole passes. The specimen was encountered on a cross vein, very narrow, similar to the oceur- rence at the Mohawk mine. The metallic mineral is inti- mately mixed with calcite. The fresh fracture is steel grey. Several fragments were digested with dilute HCl. The residue carefully washed and dried weighed 0°1968 grams. This quan- tity was dissolved in HNO, and boiled nearly to dryness in order to bring all the arsenic to the form H,AsO,. Only a trace of white insoluble material (quartz) was observed. 00683 Mg,As,O, = 0:0328 As 0:2063 CuO = 01645 Cu Hence Cu= 83°53 As = 16°55). @u: As=5:9678 100°18 Koenig—New Species Melanochaleite and Keweenawite. 415 Ff. Pulveriform chalcocite from the Champion Mine. This very interesting material was also encountered in a small cross vein and recognized by Dr. L. L. Hubbard as some- thing peculiar. Neither of us thought of chalcocite. It soils - the paper or fingers like soft pyrolusite or graphite. An aggregate of small crystals, the largest less than 0°5™™ to micro- scopic individuals. The dust appears under the microscope as made up of single hexagonal plates, or groups of plates, easily disengaged and reduced to individuals, perfectly opaque. I have since observed this same substance both at the Champion and Mass mine, dusting over groups of calcite crystals, either loosely or firmly imbedded in the calcite, causing the latter to look gray or black. It becomes bluish by tarnish. Bb. B. reacts for copper and sulphur only. The record of the quantitative analysis is lost; but I remember distinctly that the percentage of copper was close to 79. g. Nodular nuggets found in the coarse material from the mortar at the stamp mill of the Baltic mine were singled out by Mr. William Vivian as whitneyite. If seen by themselves they look much like rounded native copper; but seen along- side of the latter a difference becomes noticeable even to the untrained eye. Compared with one another, on filed or ground surface, slighter differences appear. Held in a vise, a strong blow with a cold-chisel will break the whole in two. Native copper will not do this. The fracture is hackly; there are small geodes of caicite. Calcite is visible between the imperfect crystals of gray color. But the lens also reveals minute black globular bodies. These latter I sneceeded in identifying as chalcocite. The material for analysis was extracted with diluted HCl. After extraction material weighed 0-4003 gram. It gave: Insolubles = 0°0081; Cu,S = 0°4575; Mg, As,O,= 0:0555 pelence: .Cu = 91°33 : 62 = 1-450 es: = OnGOs 75 == 0:0888 Quartz =" 2°20 100°13 Cu : As = 16'22:1 h. From Captain James Hoatson, of Calumet, I received a specimen showing quartz and what looks like native copper, at first sight. The supposed native copper is similar in color to the nodules just described; also similar in hardness and rela- tive toughness. A filed surface shows a very uniform, dense texture, with a decided yellowish, brassy, color; but etched Am, Jour. Scl.—Fourts Series, Vou. XIV, No. 84.—DECEMBER, 1902. 29 416 Koenig—New Species Melanochalcite and Keweenawite. with HNO,, the heterogeneous nature becomes visible even to the naked eye. Two fragments gave : Cu = 92°78 Ou = 93°96 1:°4755 Cu: As = 18°8:1 As = 5°85 As = 5°74 .0°0765 Cua: As =19°3:1 98°63 99°70 Two other fragments were detached close to the one whose composition has just been given. They gave: 3 Cu = 96°2 and 94°5 Ag == 38 5'5 (by difference) —— = 100°0 100°0 Here the ratios are Cu: As=30°1:1 and 25°5:1. The figures show plainly that definite proportions cannot be looked for; ~ but they indicate, as I look at it, that we must assume here conditions similar to those of pig iron, or of alloys. Further studies may give better light, especially in the direction of etching. In speaking of such alloys as these (g, 2), I ven- ture to propose the word “ Semi- Whitneyite,” to be used like Mohawk-Whitneyite, or Mohawk-Algodonite, meaning neither a species nor a variety; in the sense of a rock rather than of a mineral. Chemical Laboratory, Michigan College of Mines, Houghton, Mich. T. Holm--Studies in the Cyperacee. 417 Art. XXXIX.—Studies in the Cyperacee ; by THEO. Hou. XVII. Segregates of Carex Tolmiet Boott. (With figures in the text.) : SIMILAR to the prevalent distribution in the north the genus Carex, as represented in the Rocky Mountains of Colorado, does. not attain its greatest development until the timber-line is reached, where conditions exist which are favorable to the development of Carices. From the timber-line with the low, open thickets of willows (S. glauwcops) accompanying the water- courses, to the alpine slopes with the snow-banks, we meet with no small number of species over a relatively limited area. Those localities correspond, in many respects, with those of the north, and it is quite natural that we often find ourselves confronted with species that are, also, known to occur even in the polar-regions. Several of these alpine and subalpine Carices have been well recognized as being identical with certain northern, arctic and circumpolar, species, and we need only refer to such as: C. nardina, incurva, festiva, rupestris, atrata, misandra, etc., while others appear as indigenous only to the Rocky Mountains, e.g. Carex jilifolia, Engelmannii, elynoides, variabilis, ete. The mode of variation in alpine Carices corresponds well with that of northern species, indeed we have exactly the same variations exhibited by several of these, e. g. C. alpina, atrata, rigida, misandra, etc. And Carex variabilis, at least the plant from the Sphagnum-swamps at higher elevations in the Spruce-zone, varies so much, that we have observed forms that are absolutely analogous with the subarctic 0. anguillata, hyperborea, stans and the various forms of C. rigida, even if they may not be looked upon as specifically distinct. We have collected a number of such forms of C. variabilis growing almost side by side, and possessing the same structure and shape of utriculus, besides the same color of squamee, but vary- ing in the length of bracts, peduncles and spikes, characters that are very prominent in C. anguzllata, stans and hyper- borea ; in these species, however, the utricle offers such charac- ters as seem to afford good evidence of their specific validity, as they were formerly established by Salomon Drejer, the most eritical of Caricographers. However, the ability to distinguish and recognize several of these species from the alpine regions depends to a large extent upon observations in the field as well as a thorough acquaintance with their homologues in other countries. And one of the species, which we “intend to describe in the present paper, Carex scopulorum, offers an excellent example of analogous 418 T. Holm—Studies in the Cyperacee. variation, which might have resulted in the establishing of several species, if it were not that we had the opportunity of studying the plant in its natural surroundings. It is a species that has, so far, been entirely misunderstood, and, strange to say, 1t has at various times been confounded with such species as C. Tolmiei, rigida, vulgaris and pulla,—to none of which it bears any close resemblance.. It seems as if the mode of growth, the color, shape and direction of the utricle in this species has not heretofore been very critically examined. And the morphological structure of the rhizome with its floral and leafy shoots, besides the mere color of utriculus, its outline and direction, are characters of no small importance for distinguish- ing critical species, and are often much more constant than the - number of stigmas, of spikes, distribution of sexes, ete. Thus is the ramification of the rhizome in Carex either mono- or sympodial, the former being rare, but, as we have mentioned in a previously published paper,* it is characteristic of a number of alliés of C. laxiflora, digitata, ete., to which it appears as absolutely constant, while the latter, the sympodial, is to be observed in most of the other Carices. The cespitose and the stoloniferous growth is nearly always constant in the respective species, and such variations as have been noticed in a few cases, for instance in C. vulgaris, where a ceespitose rhi- zome changes into one that is stoloniferous, it appears to depend merely on the character of the soil, and is, therefore, of less importance. Finally we may mention an additional character derived from the foliar organs at the base of the flower-bearing stem, which was first described by Elias Fries,t and which consists in these basal leaves being provided with large, assimilating blades or being merely scale-like with rudimentary or non-developed blades, at the time of the flowering. He gave the name “ Phy]- lopodic ” to the former, and ‘ Aphyllopodic” to the latter. Besides the species with monopodial ramification, which are all “aphyllopodic,’ not a few species of those with sympodia belong to this same category. Such phyllo- and aphyllo-podic species are readily to be distinguished from each other, inas- much as the character appears constant; low forms of the aphyllopodic Carex macrocheta exhibit in this wise an entirely different aspect from the phyllopodic C. ustulata, with which such dwartfish forms have often been confounded, as well as the aphyllopodic C..cwspitosa may be distinguished at once from the phyllopodic C. vulgaris and its allies. It is a feature which deserves much attention, but seems, so far, to have been * This Journal, vol. i, 1896, p. 348. + Fries, Elias: Synopsis Caricum distigmaticarum, spicis sexu distinctis, in Scandinavia lectarum. (Botaniska Notiser, 1843, p. 97.) T. Holm—Studies in the Cyperacec. 419 overlooked or neglected by descriptive authors; as a matter of fact it constitutes one of the principal differences between C. Tolmiet Boott and our C. scopulorum, and the confusion would have been avoided had this particular point been duly considered. In respect to the utricle, the peculiar dull, brown color noticeable in C. sty/osa from Greenland and Alaska seems very rare, but is, nevertheless, also common to C. scopulorum, and constitutes, thus, an excellent distinction, and appears to be constant. A very prominent character may, also, be derived from the outline and direction of this same organ, the utricle, but it is very important to study this from life or from mate- rial preserved in alcohol. The utricle in C. scopulorum is turgid with the beak abruptly bent to the horizontal, a feature that makes the plant at once distinct from any of those to which it was formerly referred. But in regard to the other characters, such as the relative development of the spikes, their length, thickness, the peduncles, distribution of sexes, etc., several of these prove less constant and are, as we remember, often the principal foundation for the establishment of varie- ties, viz: zsogyna (C. dioica), epigejos (C. aquatilis), simpli- ctor (C. paniculata), ramosa (CU. teretiuscula), acrogyna (C. Pseudocyperus), remotifiora (C. vulpina), pendula (C. stricta), spinosa (CU. hirta), anomala (C. acuta), ete. | It, thus, appears as if there were a number of reliable points to be observed and by which one might determine obscure or imperfectly known species of the genus Carex, so as to place them in the sections where they naturally belong; but it is, nevertheless, a very difficult task to draw such distinction in so large a genus as that of Carex, when the supposed nearest related species are not at hand, but must be studied from the diagnosis alone. And in regard to Carex Tolmiei Boott it would seem absolutely fruitless to gather any knowledge about this particular plant from the latest descriptions published in this country, where the species is said, for instance, ‘‘ to repre- sent C. vulgaris Fr. on the western side of our continent,” where the true C. vulgaris Fr. is amply represented and occurs with much the same variable habit as in the old world! Moreover the diagnosis of C. Zolmiez as reproduced in recent systematic works is so as to make it “specifically distinct” from the one established by Boott; in other words, the mate- rial has not been correctly identified, nor has the original diag- nosis been carefully compared. Very little comfort is gained from consulting the larger herbaria, where we found, for instance, C. atrata, Parryana, Raynoldsii, macrocheta, ete., identified as Boott’s C. Tolmiez. Under such circumstances one feels obliged to consult the 420, T. Holm—Studies in the Cyperacee. original diagnosis as a last resource, and it is, also, the safest method. We were in the present instance under the impres- sion that our Carex from Colorado did belong to C. Tolmiez, judging from the very numerous references in literature and herbaria to the same plant from various parts of the Rocky Mountains, but our suspicion became aroused when comparing the diagnosis as written by Boott and reproduced by recent authors. Boott’s comprehensive work is, of course, a great help, but it is, as may be said of all other monographs of large genera, far from infallible, and the writer is greatly indebted to Mr. C. B. Clarke of Kew for his kindness in loaning us one of Boott’s own specimens of C. Zolmiei, and for calling our atten- tion to certain points in the figured details, which are less cor- rect. We have, thus, had the opportunity to compare one of Boott’s specimens with his diagnosis, and have succeeded in acquiring a fuller knowledge of the plant than otherwise obtainable. Most of the other species with which C. Zolmzez has been confused were already familiar to us; the remaining are evi- dently undescribed and will be treated as such, where sufficient material becomes accessible. But before we present the diag- nosis of some of these segregates, we deem it necessary to give a-few data concerning some external characters of the true C. Tolmiet Boott, by which it may be readily distinguished from its supposed allies. The species C. Zolmiez of Boott is aphyllopodic, with the rhizome densely matted and with short stolons covered by a mass of fibers from the dissolved scale-like leaves, and the sheaths of the basal, proper ones, by Boott himself cor- rectly described as: ‘ Rhizoma horizontaliter repens, fibris lanatis.” The relative large number of almost contiguous pis- tillate spikes is a striking feature, also the long and slender, setaceous peduncles of the lower spikes. The number of stig- mas is constantly three, and the utricle is, as it appears, mostly two-nerved, granular above and often purplish spotted with a short emarginate or, sometimes, slightly bidentate beak. Among the specimens which we have examined of C. Yolmiez were several which answered very well to Boott’s diagnosis of C. nigella: “A C. Tolmied differt spicis paucioribus, masculis 2-3, perigynio bidentato majore, squamis lanceolatis mucro- natis.” However, we observed among typical CO. Tolmiei utricles with bidentate beaks, and several with the scales mucronate. It, thus, appears as if C. nigella Boott may not be specifically distinct from C. Zolmzec Boott, and, moreover, Mr. Ciarke has informed us that he has examined the very specimens in herb. Boott collected by Toulmie and labelled “nigella,” and that he feels most inclined to consider them T. Holm—Studies in the Cyperacee. 421 identical with C. Tolmiei, even that they were collected from ‘“‘the same tuft” as this. It must, also, be borne in mind that the republication of C. nigella (Ill. genus Carex, p- 194) was done after the death of Boott, and Mr. Clarke, therefore, thinks that Boott himself would have reduced it. 429 T. Holm—Studies in the Cyperacee. But whatever C. nigella may be, a distinct species, a variety . or identical with C. Tolmzez, the latter itself cannot in aceord- ance with Boott’s diagnosis be confounded with any of the other species of this section, the MZelananthe Drej., among which we prefer to place it rather than among the Micro- rhynche Drej. Some authors, among which Boott himself, did think that the affinity should be looked for among the Microrhynche Drej., and he compared it with C. rigida Good., but was, nevertheless, well aware of the fact, that even if C. Tolmiet “has much the aspect and in some respects the habit of C. rigida, it differs from this in the number of spikes, the three stigmas, triquetrous achenium, etc.” Following the sug- gestion of Boott, Professor Bailey places the species among the Microrhynche, in which he includes both Drejer’s Zora- stachye and Melananthe ; thus the section becomes very unlike © that proposed by Drejer, and must be credited to Professor Bailey alone; the plant becomes, thus, associated with such species as C. vulgaris, stricta, acuta, glauca, salina, ete., a classification too unnatural to be acceptable. But then it is not so strange to understand how a number of very remote and very distinct species of no immediate affinity have been plunged together into one: “ C. Tolmzez,” the characters of which have gradually vanished in the systematic treatises of the genus in this country. And some of the plants which in this way have been united with C. Zolmiei are the species which we intend to describe in the following pages as inde- pendent species, and not by any means closely related to the original C. Tolmiet of Boott. These segregates of C. Tolmies are; Carex scopulorum Holm (figs. 1-6). (C. Tolmiet Bail. non Boott var. subsessilis Bail. ex parte.) Roots thick, very hairy ; rhizome stoloniferous, densely cov- ered with persisting (not fibrillose) scale-like leaves; culm from 10 to 40™ in height, erect, rather coarse, triangular, more or less scabrous, the base surrounded by green leaves (phyllo- podic) ; leaves shorter than the culm, relatively broad and flat, scabrous along the margins, otherwise glabrous; spikes very variable in number, from two to seven, the upper ones mostly contiguous: the terminal mostly purely staminate, sessile or short-peduncled, clavate, or sometimes androgynous or, though seldom, gyneecandrous,* the scales (fig. 4) oblong-lanceolate,; * As to the distribution of sexes and number of spikes I find in 65 speci- mens of Carex scopulorum from various localities in Wyoming, Montana, and Colorado : 42 specimens with the terminal spike purely staminate. 17 an a & ‘¢ androgynous (staminate above). 6 ey x ce ‘¢ gyneecandrous (pistillate above). T. Holin—Studies in the Cyperacee. . _ 423 obtuse, black or déep brown with thin, membranaceous mar- gins, the midrib pale, not excurrent; lateral spikes mostly three, thick, erect or spreading, when crowded near each other (fig. 3), purely pistillate or the upper ones androgynous (fig. 2), at maturity almost squarrose, the upper sessile, the lower borne on short, stout peduncles; bracts not sheathing, with black auricles, only the lower ones leaf-like and about as long as the axillary spike; scale of pistillate spike (fig. 5) ovate, acute, black with pale, not excurrent midrib; utriculus (fig. 6) minutely granular above, mostly longer than the scale, thin in texture, shortly stipitate, turgid, with a short entire beak, abruptly bent to the horizontal, dull brown, often purplish spotted above, two-nerved; caryopsis sessile, light brown, roundish in outline with both faces slightly convex ; stigmas two, base of style persisting. We found this species very abundant in the region of Clear Creek Carfion (Colo.), also near Leadville (Colo.); it grows in thickets of willows along creeks at au elevation of between 3,600 and 3,900 met.* Carex prionophylla Holm (figs. 7-11). (Carex Tolmiei Bail. non Boott var.) Roots thick, very hairy; rhizome densely cespitose with numerous persisting, very scabrous, reddish brown scale-like leaves; culms aphyllopodic, until 45°" in height, erect, stiff, triangular, very scabrous and leafy to abont the middle ; leaves of sterile shoots as long as the culm, with long, tubular sheaths, as those of the culm, very scabrous along the margins besides on both faces of the blade and on the sheaths, the blade flat ; spikes mostly five, contiguous, or the lowest one in some dis- tance from the others; the terminal staminate, short, sessile ; the scales (fig. 9) elliptical, black with pale, not excurrent mid- 24 specimens, some of the lateral spikes androgynous. 41 _ all the lateral spikes purely pistillate. de Specimens with in all 3 lateral spikes. a ee ee 9 ims ee ie 66 ce 4 4 a4 3 ee ce 1 ce iad I a4 ce 5 ce ee at ee oe 6 66 ee * Specimens examined: Wyoming: Head of Big Goose Creek, Big Horn Mts. (Fr. Tweedy); Sierra Madre Mts., Carbon County. Battle Lake Mt., 9,500 ft., scarce on a wet, shaded north-slope (A. Nelson) ; Little Goose Creek (A. Nelson). Montana: Old Hollowtop, near Pony Mt. (P. A. Rydberg and H. A. Bessey). Colorado: Marshall Pass, 12,000 ft. abundant in wet. places, covering extensive areas (C. F. Baker); Silverplume (P. A. Rydberg) ; Headwaters of Clear Creek and the alpine ridges lying east of Middle Park (C. C. Parry); abundant along Quail Creek near Stevens’ mine, in low thickets of Salix giauwcops ; Headwaters of Clear Creek ; in swamps on Gray’s peak ; very frequent in swamps on Mt. Massive near Leadville (the author). 494 _ I. Holm—Studies in the Cyperacec. rib ; pistillate spikes very short, about $™ in length, sessile, the lowest one subtended by a sheathless leaf-like bract, reaching to the base of the staminate spike, the other bracts scale-like, bristle-pointed ; -scales (fig. 10) ovate-acuminate, black with excurrent pale midrib; utricle mostly shorter and broader than the scale (fig. 11), rhombic-oval, compressed, stipitate, granular, brownish green with purplish spots, membranaceous, with a short, straight, emarginate beak, obscurely two-nerved ; stig- mas two with the style enclosed ; caryopsis immature. Habitat: Northern Idaho. Region of the Ceur d’Alene Mountains; near mountain streams; Divide between St. Joe and Clearwater River. Alt. 1,510". July 10, 1895; collected by John B. Leiberg. Carex gymnoclada Holm (figs. 12-14). (C. Tolmiez Bail. non Boott var. angusta Bail. ex parte.) Roots thick, densely hairy ; rhizome stoloniferous with shin- ing, reddish brown persisting, scale-like leaves; culm from ¥8 to 44° in height, erect, slender, triangular, scabrous, leafless, phyllopodic ; leaves as long as the culm, narrow, flat, scabrous along the margins; spikes few, mostly three, 1™ in length, situated near the apex of the culm, but not contiguous; the terminal staminate or, sometimes, androgynous, short-pedunceled ; the scales (fig. 13) somewhat spathulate-oblong, deep brown with pale, not excurrent midrib; lateral spikes pistillate, mostly two, erect, sessile or nearly so; bracts not sheathing, with _ black auricles, the lower leaf-like and reaching to the staminate spike; scales of pistillate spike (fig. 14) elongated oval, black with pale, not excurrent midrib, shorter and narrower than the utricle; the utricle minutely granular, especially above, with a few prickle-like projections near the beak and around the ori- fice of this, membranaceons, rhombic-oval, stipitate, compressed, with a short, entire beak, yellowish green, obscurely two- nerved ; caryopsis sessile, light brown, oblong; stigmas two, style flexuous within the utricle. Habitat: Eastern Oregon, bogs of Hurricane Creek, 6,000 ft. alt. Aug. 28, 1900, collected by Wm. OC. Cusick. In considering these segregates of Carex Tolmiei Boott, C. scopulorum is at once distinguished by being phyllopodic, by its turgid utricle, the two stigmas, etce.; C. prionophylla differs from C. Tolmiei especially by its profuse, scabrous covering, its small spikes and two stigmas, and C. gymnoclada by being phyllopodic, besides by the spikes not being contiguous, by the structure of utriculus and the two stigmas. Carex scopu- lorum may be placed among the JZicrorhynche Dre}j., where it is somewhat anomalous, however, on account of the turgid _ LT. Holm—Studies in the Cyperacee. 425 utricle ; C. prionophylla shows some attinity to C. cespitose L. of the same section, and (. gymnoclada may be placed with this near C. vulgaris Fr. Brookland, D. C. 426 Ford—Chemical Composition of Dumortierite. Art. XL.—On the Chemical Composition of Dumortierite ; by W. E. Forp. Introduction.—Dumortierite was first discovered near Beau- nan, France, by Gonnard, who recognized it as a new mineral and named it after the paleontologist, Eugene Dumortier.* The mineral occurs at the original locality rather sparingly as fine grains or needles enclosed in pegmatite, associated with a gneiss. Sufficient material, however, was obtained for an analysis which was made by Damourt while the optical prop- erties of the mineral were studied by Bertrand.t Dumorti- erite was next found near Harlem, Manhattan Island, New York, where it occurs in a pegmatoid portion of a biotite gneiss. ‘The mineral from this locality was first thought to be indicolite, the blue variety of tourmaline. An analysis, how- ever by Riggs, anda study of the optical properties by Diller proved that it was not tourmaline, but presumably a new min- eral. Later it was shown by E. S. Dana to be identical with the dumortierite of the French locality.| A little later the mineral was discovered at Clip, Yuma County, Arizona, and two analyses of material from this last locality, together with one of the Harlem material, were made by Whitfield.4] All of the five analyses thus far published show considerable variation in the composition of the mineral and none of them yield a satisfactory formula. The original analysis by Damour showed the mineral to be essentially an aluminium silicate con- taining a small amount of water. The presence of boron evi- dently was not suspected. The analysis, it should be stated, was made on a limited quantity of material, only 0°41 gr. being used. The analysis by Riggs of the Harlem dumortierite showed the presence of B,O, and also a considerable ‘amount of alkalies. The presence of alkalies has given rise to some ques- tion as to the purity of the material analyzed, while Whittield ascribes the B,O, to the possible presence of tourmaline. The amount of B,O, found by Riggs was about 4 per cent ; hence, since tourmaline contains only about 10 per cent of B,O,, it would be necessary, according to Whitfield’s hypothesis, to assume the presence of over 40 per cent of tourmaline in the material analyzed, a supposition quite untenable, as indicated by the proportions of the other constituents found by Riggs. The analyses by Whitfield of dumortierite from Harlem and Clip are discordant, since only a trace of B,O, is reported in the Harlem mineral, while varying amounts, 4°94 and 2°62, are indicated in the two analyses of material from Clip. Of the Harlem material only 0:217 gr. was available for analysis and a * Bull. Soc. Min., iv, 2, 1881. + Ibid., iv, 6, 1881. t Ibid., iv, 9, 1881. $ This Journal (3), xxxiv, 406, 1887. || Ibid. (3), xxxvii, 216, 1889. “| Ibid., xxxvii, 216, 1889. Ford—Chemical Composition of Dumortierite. 427 direct determination of B,O, was not made. It is stated, however, that but the smallest trace of B,O, was observed. It may here be noted that it is not especially easy to get a satis- factory qualitative test for boron in dumortierite, and without a quantitative determination one might easily be led to a wholly misleading conception as to the amount of B,O, present; hence it cannot be assumed that the absence of notable quan- tities of boron in the Harlem mineral has been satisfactorily proved. It has been found, as will be shown in the course of this article, that the dumortierite from Harlem does contain boron, and it also occurs in notable quantities in the mineral from the original locality in France, as indicated by a distinct qualitative test made by fusing on platinum wire with potas- sium bisulphate and fluorspar; hence, boron seems to be an unfailing constituent of dumortierite. All analyses thus far made agree in indicating that dumor- tierite is a very basic silicate of aluminium, yielding a small loss of weight on ignition, presumably water, but they show marked variations as regards boron. The present investiga- tion was undertaken, therefore, with the idea of making a special feature of the boron determination and of establishing, if possible, the exact chemical composition of the species. Material for Analysis.—It was possible to obtain material from three independent sources, Clip, Arizona; Harlem, New York; and San Diego Co., California. From the first locality material was obtained from specimens in the Brush collection, and also from an abundant supply of the mineral sent by Mr. Geo. L. English of New York. The cumortierite from Clip occurs as small columnar aggregates imbedded in a matrix of granular quartz, associated with a little magnetite and cyanite. Pure material was separated by pulverizing a large quantity of the rock and treating, first with potassinm mercuric iodide in order to separate the quartz, then by suspension in barium mercuric iodide so as to obtain the mineral in condition of greatest possible purity. After separation in this manner the dumortierite was picked over carefully by hand and then allowed to stand for several days in hydrofluoric acid in order to remove any remaining traces of quartz which might be attached to the mineral. It may be stated that hydrofluoric acid in the cold has practically no action on crystals of dumortierite. _Material from Harlem was obtained from specimens in the Brush collection and rendered pure by the means. described above. The material from San Diego Co., California, was obtained from some specimens which were sent to Prof. S. L. Penfield by Mr. E. Schernikow of New York. The general locality of the occurrence of this type of dumortierite has been confirmed by Mr. W. Tassin of the U. S. National Museum in Washington, who kindly sent a specimen for comparison with 428 Ford—Chemical Composition of Dumortierite. the material that was analyzed. The exact locality from which the mineral came could not, however, be learned. This mate- rial shows a marked difference in appearance from that of dumortierite from other known localities, as it has a pro- nounced lavender color rather than blue. The pleochronism of this type is analogous to other dumortierite, but ranges from deep lavender to colorless instead of from deep blue to color- less. The optical orientation of the crystals is the same as in the case of the dumortierite from Clip. It occurs in masses of considerable size, of radiating columnar structure, associ- ated with granular quartz and a light colored mica from which it was easily separated by means of the heavy solutions, and thus obtained in a pure condition. | Method of Analysis—The method of analysis presents no new features and need be only briefly discussed. The silica, alumina, and ferric oxide were determined as usual. Boron was determined by the Gooch method* using the precautions suggested by Pentield and Sperry, recorded in their paper on the Composition of Howlhtet and by Penfield and Foote in their paper on the Composition of Tourmaline.t It was found that water could not be determined by simple loss on ignition and, accordingly, the method suggested by Penfield§ of igniting with a weighed quantity of lime, was employed. The loss on ignition in this case was found to be less than when the min- eral was ignited alone. A somewhat different method of analysis had to be adopted in the case of the dumortierite from Harlem on account of the small amount of material available, and it is fully realized that the results are not to be looked upon as being as exact as those of the other analyses. The analysis was made on only 0°6 gr. of the mineral, which it was necessary to divide into two portions. In one of these, water was determined in the manner described above, and in the other boric oxide and the remaining constituents, silica, alumina and ferric oxide. The results of the analyses are as follows: Analysis No. I. Dumortierite from Clip, Arizona. Specific gravity close to 3°319. Average. Ratios. ION wi Be 30°00 29°66 29300 29°86 "497 ALO} oS 6320 63°74 63°76 63°56 617 X%6 =a FerGioxie °23 "23 "23 “001 X6 ‘006 Boyne 5°47 5°06 5°26 1: > COF0RS "420 HO) ase 1°45 1°38 1°41 “070X2 *140 100°32 4°268 4°268 : 497 = 60: 6°99 * Amer. Chem. Jour., ix, 23. + This Journal (3), xxxiv, 220, 1887. t Ibid. (4), vii, 97, 1899. § Ibid. (3), xxxii, 109, 1886. Lord—Chemical Composition of Dumortierite. 429 Analysis No. II. Dumortierite from San Diego Co., Cal. Specific gravity between 3°226 and 3°43. Ratios. 2 ee 30°58 509 2) ae 61°83 600 X6 = 3°600 Bete. *36 002 X6 “O12 B,O, ra 2 5°93 085 <6 510 H,0 ee ee 2°14 cL Se2 "238 100°84 _ 4°350 4°350 : 509 = 60: 7°02 _ Analysis No. III. Dumortierite from Harlem, N. Y, Specific gravity between 3°211 and 3°302. Ratios. lee ees > 2 31°24 520 Pee os. 2 (L926 596 X6 = 3'576 eer i Fo ED "0006 X 6 004 Peele 6714 ‘088 x6 528 120) Pee ee 2°09 116 <2 "232 4°340 4-340, =°520 = 60+-7°19 Discussion of Analyses.—It would seem that the chief problem in arriving at a formula for dumortierite would be the determination of the roles played by boric oxide and water, but the analyses indicate that these constituents are present in such variable proportions as not to yield definite ratios with the silica. In the first two analyses the ratios of SiO,: B,O, are respectively 7:1 and 6:1, with percentages of H,O increasing with increase of B,Q,. Tt may be assumed, therefore, that the boron in the mineral has not the nature of an acid element, occurring in a definite proportion, but must be considered rather as having basic qualities, replacing alu- minium as an isomorphous constituent. Moreover, there is no simple relation between the H,O and the other oxides, which fact, taken‘ with that of the small amount of water present and the difficulty with which it is driven off from the min- eral, has led to the assumption that it, too, plays the part of a basic constituent in the composition of the ‘mineral. That water does at times play such a réle has been abundantly proven. The results of the analyses were, therefore, treated as follows: The ratio of each of the basic oxides was multi- plied by a number which represented its equivalent in hydro- gen, and in this way an expression for the acid from which dumortierite is derived was obtained. Thus treated sag No. I gives the ratio of SiO,: H = 6:99:60, No. II, 7:02: 60 430 FHord—Chemical Composition of Dumortierite. and No. III, 7:19:60, the ratios of all three being very close to 7:60. Analysis No. II] shows the greatest variation from this ratio but the method of analysis which had to be employed in this case, as explained above, would account for a high ratio of the SiO,. The ratio as given leads to an acid having the empirical formula, HS. 5. ‘and, on the assumption that the hydrogens are wholly replaced by aluminium, the formula becomes Al,,8i,0O,, or developed as a basic orthosilicate, (A10),,A1,(Si0,),.. In the foregoing formula it must be under- stood that boron and a little hydrogen replace a portion of the aluminium. In Analysis I, in which the ratio of B,O,: SiO,= 1:7, the formula approximates very closely to [ AlO],,A1,B, (SiO,),.. The theoretical percentages penta oe to this formula are as follows: SiON gist PM ey ome BIO Sous. Ua agere eb BeOican Ase wis Caan 4:97 100°00 It is of interest to note here a new occurrence of dumer- tierite. During the preparation of this article a blue mineral was sent to Prof. E. 8. Dana for determination by Mr. R. M. Brereton of Woodstock, Oregon, and which was examined by the present writer. It proved to be dumortierite of a some- what new habit. The mineral occurs in small spherules, about 1™= in diameter, imbedded in a_ light-colored, fine-grained siliceous gangue. Each spherule when broken shows a radi- ated fibrous structure, and the mineral has a beautiful blue color. When the gangue is pure white a polished specimen of this material gives a very pleasing effect. This dumor- tierite shows the pleochroism characteristic of the blue variety. It was scarcely possible to obtain material sufficiently pure for analysis, but a decisive qualitative test for boron and approxi- mate determinations of the other constituents left no doubt as to the identity of the mineral. The locality of this occurrence of dumortierite as given by Mr. Brereton is on the headwaters of the North Fork of the Washougal River in Skamania County, Washington. The writer wishes to express his obligations to Messrs. English and Schermikow for the material which they gave for analysis and to Prof. S. L. Penfield for his constant advice and assistance. Sheffield Laboratory of Mineralogy, Yale University, New Haven. J. S. Hmerson—Some Characteristics of Kau. 431 Art. XLI.—Some Characteristics of Kau ;* by J.S. EMERSON. Or the Hawaiian group of islands, Hawaii is the largest, the most lofty and the most recent. The fires of its voleanoes are still burning, and from time to time new material is poured out over the surface of a land which is still in process of forma-~ tion. Here is the place to study Nature in her workshop and see a world in making. But it is not of Hawaii as a whole that we propose to speak. It is made up of districts with characteristics marked and distinct from one another. The Hilo-Hamakua-E. Kohala district, occupying the north- east side of the island, from Hilo Bay to Upolu Point, is the land of gulches and streams of water, of disintegrated rock © and deep heavy soil. The W. Kohala-Kona-W. Kau district, occupying the west side of the island from Upolu Point to South Cape, is the land of slowly disintegrating rock, almost without gulches and running streams. The extreme richness of its coffee lands is due to the fact that new soil is ever being formed, as wanted, _ from the loose mass of aa rocks, which contains every element needed for plant growth. Puna is the district where frequent showers fall upon loose stone and sink out of sight, without forming gullies and streams, and where vegetation thrives without soil. Here the cocoanut tree grows in immense forests as nowhere else in this group. Kau is unique, a district by itself; “Aaw ka maka lepo”’; Kau the dusty. That portion extending from South Cape to and including Kapapala Ranch, a distance of some thirty miles, contains all the land of any value for grazing or agri- culture. Briefly described, it is a wide expanse of compara- tively modern lava, forming a floor of rock upon which is spread a superficial covering of fine, light, reddish or yellowish dust of varying depth. In places the ephemeral mountain torrents have washed away this unstable soil and revealed the bed rock beneath, which has scarcely yet begun to disintegrate and ally itself with earth. This superficial coating of dust is distinct from the rocky stratum on which it rests, as the dust which the cleanly housewife removes is from the floor which she has swept. And such dust as that of Kau is found in quantity in no other district of these islands. In the olden days the natives of this section, when engaging in the popular pastime of lehe kawa, jumping from a high bank, often sub- stituted a bath of this dust for the usual pool of water. An * Read before the Social Science Association of Honolulu, Oct. 14, 1895.. Am. JOUR. SCI.—FouRTH SERIES, VOL. XIV, No. 84.—DecEmBER, 1902. © 432 J. S. Emerson—Some Characteristics of Kau. ordinary dirt road, unless properly covered with stone, is quickly worn down by constant travel. The wheels of loaded teams sink into the soil, which in time is blown away by the winds, or washed out by the heavy rains which occasionally fall. From Waiohinu to Hilea the cane fields are mostly on the hills, where the soil is of great depth and remarkably free from rocks or stones, so that almost anywhere a crow bar or walking stick can readily be thrust down to its full length. On the low lands, however, the soil is usually shallow, with the bed rock frequently cropping out, or may be wanting altogether. The Hawaiian Agricultural Co. are more fortunate in the lay of their plantation, and have an extensive tract of about four thousand acres of rich cane land, not perched on isolated hills, but occupying two large valleys with the gentle slopes between them. These fields are somewhat scattered about, with unpro- ductive areas between them, but as a whole they are far more compact and accessible than the fields from Waiohinu to Hilea. Kau is not a well-watered district. It often suffers from prolonged drought, when the dry winds parch and destroy whole fields of young cane and raise clouds of dust from the newly plowed lands. When at length the long wished for rain comes, it sometimes pours down in such torrents as to cause great destruc- tion of property. The light soil soon dries up again, so that the irregularity of the rains is the more keenly felt, while the cane stalks register the fact in the varying and irregular length and diameter of their joints. During these periods of drought great care has to be exercised to prevent any one from smok- ing in the fields or making a fire in the grass, for when a fire is once started, it is sometimes extremely difficult to prevent it from spreading under ground. The roots and other vegetable matter in the soil are consumed, while the mineral basis of the soil itself is so light and spongy as to allow enough air to enter to support combustion many inches below the surface. At times, when such a fire was supposed to be extinguished, it has burrowed its way unobserved, to show its presence at some other point where the surface would cave in and the ground itself seemed on fire. Mr. W. E. Rowell states that “one peculiarity of the soil on the Pahala plantation is the entire absence of any clay or anything adhesive in its composition, so that it does not stick to the shoes, however wet it may be.” At various points through the district it is possible to exam- ine the record of the rocks and to see the character of the suc- cessive strata resting one upon another. It would appear from ° such observations that most of the strata represent ordinary lava flows, with but thin separating sheets of ash or earth. But Providence has most considerately anticipated the indas- trial wants of man at the present time, and above all these © J. 8. Emerson—Some Characteristics of Kau. 433 successive layers of rock has added this crowning layer of dust, which makes it possible to plow and planta district whose formation is so recent. How different it might have been if this superficial layer had been aa@ or pahoehoe rock, as in Kona, requiring another ten thousand years to distintegate it suffi- ciently for farming purposes. Between the South Point and the road from Kahuku Ranch to Waiohinu is a beautiful sketch of smooth grassy pasture. At various points near the Cape the writer has measured the depth of the soil to the bed rock, and recorded it as having an average thickness of about ten feet, separated into two layers of nearly equal thickness by a thin layer of whitish earth per- haps half an inch thick. One branch of the flow of 1868 traversed a portion of this plain from the vicinity of the Kahuku Ranch house half way to the Kaalualu landing. Flows of an earlier date have also covered other portions with a horrid mass of rock. But it is ontside of the purpose of this paper to describe the various lava flows which cover much of the territory below the cane lands and the Kapapala Ranch. The woods above the plantations are difficult, if not posi- tively dangerous, to traverse on horseback, so much so that Mr. Julian Monsarrat, who knows the country well, pronounced the carrying of supplies throngh these woods to his workmen engaged in building a fence along their upper edge, as impracti- cable. ‘The soft treacherous mnd gives no foothold for man or beast. Consequently the supplies were carried a long distance around. The Kau hills, Iholena, Puu Enuhe, Makanao and Kapuna, bear a most striking family resemblance to each other, so that the profile of one will serve pretty well for all. Cap- tain Dutton in his Hawaiian Volcanoes speaks of them as “mere remnants of a large alluvial formation which was origi- nally continuous,” and the valleys which separate them as “ val- leys of erosion.” In speaking of these hills he uses the follow- ing language: “The more we see of this country the more will the evidences accumulate that these buttes are silent wit- nesses of an extensive upheaval of this part of the island at an epoch not very remote.” Again he says, “It is difficult to estimate with precision the amount of elevation attested by these terraces, but there are evidences still legible of several of them—one of them 1,200 to 1,400 feet high, another about 2,800, and perhaps, though more doubtful, a third at 3,400 feet.” (See Dutton’s Hawaiian Volcanoes, page 98.) This theory, though advanced by a recognized authority on the geology of portions of the western United States, lacks the support of facts. It has not a single ledge of coral, a bed of shells, or a vestige of marine life of any sort on which to rest. 434 J. S. Emerson—Some Characteristics of Kau. Until such proof of marine origin is found, we cannot accept the theory of upheaval as proven or even as a working hypoth- esis. ‘To speak of the Kau dust as an “alluvial formation ” only removes the question of its origin one step further back. Whence came it? The process of disintegration has scarcely begun in much of the Kau bed rock. The most casual study of its soil shows that it is not decomposed rock. It is totally unlike the soil of Hilo or Kona, and certainly was not washed down from the aa and pahoehoe of upper Mauna Loa. Evidently it is a formation similar to that which covers a large portion of the slopes of Vesuvius and overwhelmed the ancient city of Pompeii. This volcanic ash is the evidence of a series of explosive eruptions in Kan on the grandest scale, probably far surpassing anything of a similar nature of which we have any evidence in this group. We must then look to the medium of the atmosphere rather than to the action of water to explain the remarkable distribution of this dust which has been sifted down on the ridges, as well as in the hoilows, in a manner far more regular and uniform than could have been accomplished by the action of running water. To locate the source or sources of this aérial eruption is a problem not yet fully solved, but some light may be thrown upon it. We need hardly look to Mokuaweoweo, the summit crater of Mauna Loa, as asource. Tor had such an explosion occurred there, the dust would also have been earried in the direction of Kona. But asa fact, neither in Kona nor on any side of the great dome of Mauna Loa is this dust found in quantity, until we reach the wood belt of Kau. Kilauea, the only remaining active voleano, may be looked to as a possible source with slightly greater probability. But between the district covered by the Kau dust and Kilauea lies the Kau Desert with an area of “many miles” of a totally different formation, while nothing is to be seen of the dust anywhere around the voleano. The writer has examined fissures in the Kau Desert to a depth of. perhaps thirty feet and failed to see any of the dust. If then Kilauea were the real source of the dust eruption, the evidences of it have been covered most com- pletely by these later eruptions. | The supposition is barely possible, but extremely improbable. Another possible source in this enumeration should not be over- looked. It is the vicinity of Puu o Keokeo, greatest of all the offsprings of Mauna Loa, with an elevation of 6870 feet; it appears to those who sail around South Point as another grand mountain, the rival of its mighty parent. It is located on the great fissure, or rift, in Mauna Loa, extending from Pohakn Hanalei to the vicinity of South Cape. This fissure, probably as old as the mountain itself, lies in the direction of the line J. S. Emerson—Some Characteristics of Kau. 435 joining Mauna Kea and Mauna Loa, the same as the line of the axis of Mokuaweoweo produced. The flows of 1868 and of 18587 seem to have escaped from the central shaft through this lateral rift in the mountain, and to have come to the sur- face at points on this line of least resistance. It is an axis of great volcanic activity, which has built up for itself the immense ridge of Mauna Loa which divides the geological district of Kau from that of Kona. About Puu o Keokeo as a center there is a large area cevered with pumice and gravel, quite similar to the so called Kau Desert, southwest of Kilauea. Manifestly it has been produced by explosive eruptions on a large scale. But as in the case of the vicinity of Kilauea, so here the peculiar Kau dust is altogether wanting. Further there is no sign of any such dust deposit at any distance, on the Kona side, of this area covered with pumice, while the entire portion of Kau covered with dust is at a distance of many miles in the opposite direction. The conclusion seems forced upon us that we must look for the origin of this great eruption within the limits of the dis- trict covered by it. With this idea guiding us, we naturally look first to the immediate vicinity of the hills already men- tioned, where the peculiar Kau soil attains its maximum depth. One cannot but be struck with the suggestion that Pun Iki marks a point on the upper rim of a vast extinct crater extend- ing south to Kaiholena, possibly even to the great whaleback ridge on which Kapuna Trig. Station is situated, while the eastern rim, now largely washed away, would be marked by the hills Makanao, Puu Enuhe and Kaumaikeohu with the steep side hill just to the east of it. Everything seems to point to this locality as the source of the stupendous explosion, or series of explosions, which has rescued Kau from being a waste of unproductive rock and transformed it to so large an extent into a land of pastures and plantations. If we admit that this is indeed the source of these eruptions, the whole problem of the distribution of the dust is greatly simplified. As would naturally be expected, the ejected matter has been deposited on all sides, but the action of the trade wind has carried the finer particles to a much greater distance to the south and southwest than in the opposite direction. So that we find the country about South Cape covered to a depth of ten feet, as before stated, with the finest dust, without any admixture of coarse material. The whole district west of Kaaluala landing has been tilted up on its western edge, along the line of the great fissure already alluded to, forming an extensive fault from the sea to the Government road just above Col. Norris’ residence. The visible deposit of dust breaks off abruptly at the edge of this precipice. But according to native. 436 J. S. Emerson—Some Characteristics of Kau. tradition the whole plane of Pakini at its base, on the Kona side, was formerly a rich field, cultivated with sugar cane and sweet potatoes. Since that time, however, various flows, among which are those of 1868 and 1887, have converted this garden into an uninhabited waste of aa and pahoehoe. If, however, we examined the earth in the vicinity of the supposed center of eruption, we find a considerable admixture in places of stones, for example the so called Mud Flow of 1868 covered several hundred acres of good land to a depth of from ten to thirty feet with a heavy, red, clayey earth, abounding in stones, wholly unfit for cultivation, and producing a grass of such inferior character that even the cattle and horses shun it. This mud flow was simply a land slide. Kaapao pali was full of water and the great earthquake of April, 1868 loosened the superficial mass of earth and lubricated the rocky bed on which it rested. Gravity acting on a steeply inclined plane did the rest. Mr. Walton, the energetic and wide-awake man- ager of the Pahala plantation, has used his wits to good advan- tage in the search for water on the Kaapao pali and neighboring hillsides, and during the past few months has found enough, as I am informed, to irrigate five hundred acres of cane. There are no traditions, so far as the writer can learn, relating to these great explosive eruptions. The only oceur- rence of the sort of which we have any historical information took place in 1790 at the volcano of Kilanea, which destroyed, as Dibble tells us, about 400 of the warriors of Keona’s army, one entire division. The sand, ashes, pumice and stones ejected at this time cover the country about the volcano for miles, and have been fully described by Dana and others. The extensive area about Pun o Keokeo already alluded to is covered with material very similar to that of the Kau Desert. The “ Alanui Umi,” built early in the 16th century by King Umi, traverses this mountain desert from north to south. This road was made necessary by Umi’s occupation with his court and warriors of the barren waste between Mauna Loa and Hualalai. When the political and military necessity for Umi’s occupation of this strategic position ceased, he sought a more agreeable home, and spent the last years of his life at Kaawaloa, by the sea. The Umi road seems to have been little used since those days, save by the race of bird catchers and perhaps by the sandal-wood cutters of a later day. Its very existence, however, is scarcely known to most of the dwellers on Hawaii. This ancient road is chiefly interesting to us at this moment as an evidence that no great explosive erup- tion has probably taken place in that portion of Hawaii for the past 350 years. Itis pretty much in the condition in which Umi left it. J. S. Emerson—Some Characteristics of Kau. 437 Some years since I had occasion to ride overa portion of this road, which was two or three feet wide and is still readily fol- lowed. So long as the mule kept to the old path he made good progress, but when he deviated but a few feet on either side, he sank down to his girth in the sand and pumice and floundered helplessly. It was most instructive to follow this path to the great natural amphitheatre on the southern slope of Puu o Keokeo, where the famous cock fights used to draw immense crowds to witness one of the great national games of Hawaii. The cock-pits or rather pens still stand, probably as Umi left them three and a half centuriesago. Had there been a shower of ashes or pumice from the vicinity of Puu o Keo- keo during this interval, the old road and these cock-pits would have disappeared forever beneath the sands of the desert. Since the above was written, Dr. A. B. Lyons of Oahu Col- lege has kindly furnished the following statement: ‘“ I have had occasion to examine the soil from some of the cane fields at Pahala. They were remarkable in several particulars. They contain a large proportion of organic matter, and yet could not be called peaty. They seemed rather sandy. They contain almost no clay. The mineral matter consists in fact of vol- eanic sand rich in olivine and very little decomposed—very similar in many respects to the sandy or gravelly soil of Punahou, which is made from recent voleanic sand. The abundance of lime in the soil confirmed also this view of its probable origin. Hawaiian soils composed of decomposed lava contain very little lime.” For the sake of clearness, a brief recapitulation and summing up of the argument with reference to the origin of the pecu- liar Kau soil may properly conclude this paper. A district equal in extent to one-half the area of the Island of Oahu, 300 square miles, is covered with a soil quite unlike that of any adjoining district, and totally distinct from the very recent voleanic bed rock on which much of it rests. The entire absence of a single ledge of coral, bed of shells, or other positive evidence of marine formation, and the frequent occur- rence of caves and caverns which remain unfilled with silt, together with the very porous character of the whole formation, diseredits the theory “of an extensive upheaval of this part of the island at” any “epoch not very remote.” On the contrary, this formation originated on dry land and has not been sub- merged. If this soil were alluvial it would show stratification. Instead of that it is blanketed like newly fallen snow upon the uneven contour of hill, plain and ridge. | If this formation were deposited at tide level, it would be interpenetrated by marine growths, animal and vegetable. But the evidence that such growth exists is conspicuously wanting. 438 J. S. Emerson—Some Charucteristics of Kau. But, finally, no better evidence as to the origin of this minute sand can be produced than its appearance under the mierc- scope. Its mechanical features are sharp and broken as of volcanic sand, wholly unlike the rounded and worn features of beach sand. In short, the positive testimony of chemical analy- sis and microscopic examination shows that the mineral portion of this soil is voleanic sand, not the wash from any higher level of decomposed rock. This necessitates the theory of explosive eruptions on a scale of magnitude proportional to the extent of territory covered, which ‘would have been greater but for the ocean which abruptly terminates it along the entire coast from Punaluu to South Cape, and a precipice on the southwest, beyond which all trace of this soil has been effectually covered up by flows of lava. Further, three great centers of volcanic activity, viz., Kilanea, Mokuaweoweo and the vicinity of Puuo Keokeo to the northeast, north and west respectively of the district in question, have covered extensive areas about them with other formations, so that it is impossible to locate the original limits of this unique formation in those directions. At the same time, the evidence is very strong, if not conclusive, that neither of these three volcanic centers was its source, while every consideration points to the great crater-like area below Puu Iki. This locality is so little known and so difficult of exploration that we are unable to point out the exact location of the center of explosion. The unstable character of the material ejected would tend in a measure to cover up its source, which from the nature of the case could not be as sharply defined as that of a flow of aa or pahoehoe, whose birthplace is marked with solid rock. As to the time when these remarkable explosions occurred, it may be observed that the only event of this character in these islands, of which we have any definite information, took place at Kilauea a little over one hundred years ago, as already stated. From the fact that the old cock-pits near Puu o Keokeo and the ancient road leading to them remain as they must have been left by King Umi 350 yearsago, it seems quite evident that no explosive eruptions on a large scale have taken place during that interval either from the summit crater of Mauna Loa or from the great lateral rift which has been so active in building up the immense ridge which marks its southwest slope. The conclusion therefore is evident that the eruption which produced the Kau dust under discussion was earlier than the beginning of the sixteenth century. Though we may not locate the time of these eruptions as definitely as the place, yet the fact that they form the last of a long EE a ee J. S. Emerson —Some Characteristics of Kau. 439 series of distinct strata, each of which represents a consider- able interval of time, shows that they must have occurred at a period very recent in the growth of the island. On the other hand, the entire absence of any tradition relating to them and the occurrence in several places of aa and possibly pahoehoe flows from Mauna Loa of limited extent and of uncertain age superimposed on this formation, make it probable that the stu- pendous convulsions of Nature which gave birth to this crown- ing feature of the district and prepared it for the support of man in an advanced stage of civilization, occurred many cen- turies ago, probably before the advent to these shores of its first Polynesian inhabitants. 440 Phelps—Tirtrimetric Estimation of Nitric Acid. Art. XLIIT.—The Titrimetric Estimation of Nitric Acid ; by I. K. PHetps. [Contributions from the Kent Chemical Laboratory of Yale University—No. CXIII.} In the methods for the quantitative estimation of nitric acid which depend upon its reduction with a ferrous salt and the determination of the amount of oxidation produced, serupu- lous care is necessary that the atmosphere in contact with the ferrous salt while the nitrogen dioxide is present shall be free from oxygen. This fact was recognized by Fresenius,* who modified the original process of Pelouzet by filling the flask with carbon dioxide or hydrogen at the outset. HEdert used carbon dioxide similarly. Holland’s method,§ roughly described, consists in boiling, until the air is expelled, the solu- tion of the nitrate in a flask provided with a doubly bent exit tube, rubber-jointed and fitted with a pinch cock, then admit- ting through the tube as the flask cools a mixture of ferrous salt and strong hydrochloric acid, heating the mixture on a water bath, and, finally, titrating the resulting ferric salt with stannous chloride. All of these methods give results which are higher than the theoretically expected—those which use carbon dioxide on account of the oxygen invariably present in the gas as ordi- narily produced in the laboratory, and Holland’s process pos- sibly because of the slow leakage through the rubber connections during the long heating, or because the nitrogen dioxide, which is not driven out completely from the solution of the iron salts, acts somewhat with the atmospheric oxygen during the titra- tion. Another series of methods has depended upon the deter- mination of the nitrogen dioxide evolved, usually by direct measurement as nitrogen dioxide. Among ‘these may be men- tioned the methods of Schloessing, | Reichart,{ Schulze and Wulfert,** Tiemann,t+ Wildt and Scheibe,t{ Warington,$$ Boehmer, | | Kratschmer, Wilfarth,*** Morse and Linn.,t++ Berger,tt{ and Roberts.§§$ In general, these methods give results lower than demanded by the theory—in many cases, on * Ann., cvi, 217; Zeit. anal. Chem., i, 32. + Ann. de Chim. Phys. [3], xx, 129. t Zeit. anal. Chem., xvi. 267. § Chem. News, xvii, 219. | Ann. de Chim. Phys. [8], xl, 479. “| Zeit. anal. Chem., ix, 26. ** Chid.. ix, 400 ++ Anleitung zur Untersuchung von Wasser von W. Kubel. Zweite Auflage von F, Tiemann, 55. tt Zeit. anal. Chem., xxiii, 151. S$ Jour. Chem. Soc., , xxxviil, 468; xli, 345. |||| Zeit. anal. Chem., "xxii, 20). “[4] Ibid., xxvi, 608. eet Dbid:. aos, 411, ttt Amer. Chem. Jour. , viii, 274. ttt Chem. Zeit., xix, 305. S85 This Journal, xlvi, 126 (1893). Phelps—Titrimetric Estimation of Nitric Acid. 441 account of the solubility of the nitrogen dioxide in the ferrous solution used as a reducer and, in other cases, on account of the solubility of that gas in the solution of sodium hydroxide over which it is measured. Further there is the effect of oxygen upon the nitrogen dioxide; if present in the measur- ing burette in the proportions found in air, it will not give any appreciable effect in moderate amounts, as was observed by Roberts; but if it is present while the gas is in con- tact with the ferrous solution, the nitrous or nitric acid formed will be taken up by the solution, and, should the oxygen be introduced continuously, as an impurity in carbon dioxide furnished by a Kipp generator, the iron salts will never be free from oxidized nitrogen. If, however, the oxygen is present in some other proportion of dilution than that of the air—as, for example, in the proportion in which it dissolves in aqueous solutions—it will produce an error no matter whether it comes in contact with the gases of the ferrous solution or those of the collecting burette: in the example taken, the proportion of oxygen being greater than that in the air, the error produced is one of deficiency. The effect of oxygen has been recog- nized before. For example, in his process of determining nitrates by reducing them with ferrous salt and hydrochloric acid in an atmosphere of carbon dioxide (furnished by the action of hydrochloric acid on marble), boiling the ferrous solu- tion completely to dryness, collecting the gases over mercury, absorbing the carbon dioxide by sodium hydroxide solution and the nitrogen dioxide by repeated treatment with a con- eentrated solution of ferrous salt, Warington found that, when the carbon dioxide was made as free from air as possible by using marble boiled in water and hydrochloric acid also boiled and adding a little cuprous chloride to the acid, the results were decidedly better. The estimation of the amount of oxidation of a ferrous salt may be accomplished with a simpler apparatus than that required when the nitrogen dioxide is measured, and the purpose of this article is to put on record such a method, following most nearly the procedure of Holland. The apparatus used consisted of a 250 flask closed with a rubber stopper carrying in two perforations the inlet and exit tubes. A stoppered funnel of 50°* capacity with its tube constricted at its lower end was used as the inlet tube; and a glass tube of ‘8° internal diam- eter, enlarged just above the stopper to a small bulb (to pre- vent mechanical loss of the solid contents of the flask during the boiling) and bent twice at right angles, served as the exit tube. The analysis was made as follows: A solution of ferrous sulphate, mildly acidified with sulphuric acid, was made of 442 Phelps—Titrimetric Estimation of Nitric Acid. about one-fifth normal strength and standardized against stand- ard decinormal arsenious acid solution by treating portions of it, measured from a burette (and weighed as a check on the burette readings) with an excess of decinormal iodine solution, adding about 3 grms. of Rochelle salt in solution, neutralizing with acid potassium. carbonate and adding in succession 15°%™ of a saturated solution of acid potassium carbonate, starch paste and then standard arsenious acid solution to the bleaching of the starch blue, and, finally, titrating to color with the iodine solution. For the determination of nitric acid, the pure potassium nitrate of commerce was used. In the smaller amounts, the nitrate was taken in a solution of known strength measured from a burette and in the larger amounts as the dry salt. Where the solution of nitrate was used, it was measured into the flask, the stem of the separating funnel being com- pletely filled with water, and the exit tube of the flask reach- ing to the surface of mercury which was placed in a test tube to the depth of about three centimeters. The nitrate solution was then boiled to small volume, an amount of the standardized ferrous sulphate solution known to be in excess introduced into the separating funnel, the exit tube plunged a centimeter or two deep into the mercury (which is readily accomplished by changing the position of the flask on the wire gauze provided that the gauze is depressed well at the center and the flask is set well up on the higher part at the beginning of the opera- tion), and then the flame withdrawn until diminution of pres- sure sufficient to draw the ferrous solution into the flask is made evident by the rise of the mercury in the exit tube. By applying and. withdrawing the flame and by regulating the rate of inflow of the solution, the ferrous salt may be intro- duced without admitting air and the funnel washed carefully with an amount of concentrated hydrochloric acid nearly enough to equal the total volume of the liquid in the flask. After the pressure has been restored in the apparatus by heat- ing the flask, the exit tube is again raised to the surface of the mercury and the solution in the flask boiled to a volume of 10-15". The excess of acid is then nearly neutralized with sodium carbonate solution, the carbon dioxide evolved assisting in maintaining the pressure in the apparatus so that the con- densed liquid in the test tube which may contain oxidized nitrogen dioxide is not returned to the iron solution ; the flask is cooled and the ferrous salt remaining determined by iodine as previously described or by a standard solution of potassium permanganate. in case permanganate is used, the contents of the flask are diluted with 600° of water, 2-3 grms. of crystal- lized manganous chloride,* and titrated to color with potassium * Gooch and Peters, this Journal, vii, 461 (1899). Phelps—Titrimetrie Estimation of Nitric Acid. 448 permanganate. In the experiments where the dry salt was used, the air was expelled from the apparatus by boiling 10°" of water to small volume in the flask, arranged as previously described, the ferrous sulphate solution introduced and concen- trated by boiling to a volume of about 20°™* so that the amount of acid used may not be so large; then, the nitrate, dissolved in a small amount of water, was allowed to flow in and was finally washed in, as before, with an amount of concentrated hydrochloric acid, which approximates in volume that of the liquid contents of the flask. Experiments numbered I-VIII, inclusive, of the following table show the results of a series of experiments made as described above. Oxygen value Oxygen value KNO; of ferrous salt of ferrous salt Error on taken. taken. found. oxygen. erm. erm. erm. erm. "070500 0°01823 0°00621 0°00015 + II 0°0500 0°01865 0°00681 0°00003 — VE 0:0500 0°01954 0:00768 0°00000 + IV 0°1000 0°'02881 0:00507 0°00001 + VV 0°1000 0°02822 0°00441 0:00008 + VI 0:2500 0°06453 0°00512 0:00009 + VII 0:5000 0°138394 0°01524 0°00005 + VIII 05000 0712210 0:00340 000005 + IX 0:0500 0°01720 0°00747 0:002)4— ~X, 0-0500 0701550 0700389 000026 — XI 070525 0°01550 0°00318 0°00014— XII 0:1000 0°02765 0°00432 0:00040 — Experiments numbered [X and X were made to determine whether the long boiling in the previous experiments is actually necessary ; for in the work by Fresenius as well as that of Eder, directions are given merely to boil the hydrochloric acid solution of the iron salt with the nitrate until the color of the dark compound of the nitrogen dioxide with the ferrous salt wholly vanishes and is replaced by the clear color of the ferric salt, which means an active boiling of not longer than five minutes in the experiments recorded in the table. Experi- ment IX was made exactly like the similar ones above it in _ the table, except that the boiling was interrupted after the dark colored ferrous compound with the nitrogen dioxide was completely broken up; and experiment X similarly, except that the boiling was continued for five minutes after the complete disappearance of the dark color. Obviously the period of boil- ing allowed by Fresenius and Eder is not enough, but since the main error incidental to these processes is an error of excess due to oxygen present, as already stated, it will readily appear 444 Phelps—Titrimetric Estimation of Nitric Acid. how this second error, which is one of deficiency and hence correcting the first error, may have been overlooked. | Ferrous ammonium sulphate has been recommended by Austin and Chamberlain* and by Rosat as more convenient, stable, and sensitive than the crystalline ferrous sulphate. It would seem possible that nitric acid might act as an oxidizing agent on the ammonium salt, and certainly nitrous acid (if it were produced, as might be, as an intermediate product in the reduction of nitric acid to nitrogen dioxide) would act accord- ing to the equation, NH,Cl4+ HNO,=HCl1+2H,0+N.,,. Such an action either of the nitric acid or nitrous acid would produce anerror of deficiency. Experiments Xl and XII were made to test this point, being made exactly like those num- bered I-VIII, except that 1 gram of erystallized ammonium sulphate was added with the ferrous salt. The results show slight but appreciable losses. The concentration of the hydrochloric acid in this operation does not allow of much diminution under these conditions, where immediate reduction of the nitric acid without any volatilization is a necessity,—a fact which has been recognized before by Roberts and obviated under the conditions there used. Thus it would appear— First. That the method outlined above is capable of yield- ing very accurate results, affording as-it does an easy and com- plete means of shutting out oxygen from the nitrogen dioxide while that gas is in contact with the ferrous salt. Second. That prolonging the boiling only until the dark colored compound of nitrogen dioxide with ferrous salt is broken up, results in the incomplete reduction of the nitric acid. | Third. That ammonium salts must be absent, if the highest accuracy is desired. *Amer. Chem. Jour., v, 209. + Gazz. chim. ital., xv, 295. ee Lt. M. Brown—Clays of the. Boston Basin. 445 Art. XLIL.—TZhe Clays of the Boston Basin ;* by ROBERT MarsHALL Brown. THE problem of the correlation of the clays of New England has never been solved. Numerous papers have been published, in which various clay beds have been described and in part dis- cussed. Some of the writers have ventured to correlate the clays of neighboring sections. No one has yet undertaken the solution of the entire problem. Not enough light has been cast upon the subject for a general discussion. The isolation of clay, beds in the same neighborhood with no evidence to show whether they are parts of the same deposit or disconnected deposits of the same time or unrelated beds, offers little of interest. Similarity of clay itself cannot be taken asgood data for correlation, unless by chance some unique peculiarity of composition is discovered. Ordinarily, the zest to further search is furnished the student of clays by the constant excavations that are made in the streets for the laying of pipes, the opening of new clay pits, the extension of the old, and the removal of the cover of the clay for various purposes. All new exposures which furnish interesting evidence in any direction should be recorded. By the accumulation of such evidence, it is believed that in time a correlation of the clays of New England and beyond may be safely attempted. For this reason, the writer of this article desires to place on record some of the results of this field study on the clays about Boston, with a few observa- tions that arose during the process of the investigations. Field Work.—Near Chelsea Street, between the cities of Everett and Chelsea, Massachusetts, extensive excavations, during the fall of 1901, revealed the clays. A hill, drumlin- like in appearance, of no great height, and half a mile long, with a trend a little south of east, parallel to the drumlins of the neighborhood, was in part removed. An almost com- plete cross section of the hill was exposed. The core of the hill is an igneous rock (fig. 1). The rock does not extend to the southern slope, however. Here a clay and sand interior was found. Both clay and rock was capped by a thin layer of till. The relation of the clay to the rock was unknown, as neither the quarrying of the rock to the north nor the removal of the elays to the south showed the contact. The first appearance of the south end of the hill in the process of removal of the material showed an anticline in the clay. The stratification of the beds was emphasized by the interlamination of thin layers * This paper is a part of a thesis presented in the course on Glacial Geology at Harvard College, under Prof. J. B. Woodworth. 446 RL. M. Brown—Clays of the Boston Basin. A. ='Clay; Figure 1.—Chelsea Street, between Chelsea and Everett, Mass. Dotted lines in clay represent sand. 5. .> Talus, C. = Bock, D. = far: : Gi = 50.0 DOS LAGOS. G GOD: SD _— — — Figure.2.—Chelsea Street, between Chelsea and Everett, Mass. A. = Sand, Dotted lines in clay represent sand. Bo = Clay, ‘C= Tis, — 2S SS SSS SS = A Ms Oh. WAGES A. = Clay, Figure 3.—Chelsea Street, between Chelsea and Everett, Mass. Dotted lines in clay represent interstratified sand. 5: = Sand, oo tat R. M. Brown-—Clays of the Boston Basin. 447 of sand in the lower portions of the clay and by dark bands, probably of vegetable matter, in the upper portions. Below the clay was a bed of sand, and above a thin layer of till which ran out towards the south (fig. 2). The disappearance of the till was due probably to the removal of the material in a pre- vious excavation further to the west. Before a second visit to the pit was made enough material had been removed to yield a better section (fig. 3). The bed of sand at the bottom of the clay (shown in fig. 2) proved to be a stratum of sand 14 inches thick, underlain by more clay. The sand was of fine texture, Figure 4.—Cross-section of end of Drumlin in Revere, Mass. A. = Clay, B. = Sand and Clay, C. = Till. similar to our beach sands, and homogeneous throughout. A single small slate pebble was the only break in the uniformity of the sand bed. At the same time enough of the talus had been removed to show the sand bed extending to the edge of the till and there cut off before the deposit of the till. To the north the clay was much more crumpled, and the interstratified sands were, as a general rule, thicker than the layers above the thick sand bed. The till averaged 18 inches in thickness, was made up of coarse and fine material, and extended over the entire section of the hill remaining. The slope of the hill was very gradual and the question of the slipping of the till over the clays was negatived by the rolling surface of the clay as well as by the slope. In seeking for other instances of the same thing, a section across the trend of a drumlin at the junction of Shirley Avenue and Nahant Avenue in Revere, Mass., was found. The drum- lin had the northwest—southeast position of the drumlins of the district. The core of the drumlin was clay (fig. 4). Above the more solid bottom clay was a thickness of about three feet, made up of alternating layers of sand and clay, the sand increasing upwards. Over the sand was 14 feet of till. Am. Jour. Sc1.—FourtH Series, Vou. XIV, No. 84.—DrEcEmBER, 1902. ; 31 448 ft. M. Brown—Clays of the Boston Basin. The till contained bowlders of varying sizes; the largest over a foot in diameter. Thickly intermixed as a part of a till was a great deal of clay. The clay itself, below the layers of sand, was homogeneous and contained no foreign matter. The bot- tom of the clay was seen in one instance only, and the clay rested in that case on gravels. This exposure was at a distance from the two mentioned above. Clays in Literature.—An early mention of the clays was by — Edward Hitcheock.* His conclusion stated that nearly all of our clays are in the Tertiary formation. At the same time he is frank in admitting that he has no evidence bearing on the matter, and that his result was reached solely by analogy. The European plastic clays resting on the chalk was the basis of his reasoning. In the Geology of New Hampshire many cases are instanced by Uphamt where clays overlie till. This is especi- ally true of the Winnipiseogee Lake beds. His explanation is quoted: ‘“‘ The ice-sheet probably remained in a high mountain- like mass over these lakes after it had disappeared on each side from the basin of Ossipee Lake and from the lower part of the Pomigewasset valley. As the melting continued, the drainage over this area was frequently obstructed because the ice-sheet retreated from the lines of watershed towards the middle of these hydrographic basins. The water seems then to have melted large open spaces beneath the ice near its mar- gin in which beds of clay and sand were deposited. This would occur at the various heights and in the situation where these beds are found, and the till which overlies them is shown by its material to be that which was contained in the ice-sheet and fell upon the surface when its melting was completed. We thus see how these deposits came to be spread over the slopes of the hills, thinly covered by large boulders and till. The frequent accumulation of such deposits in other parts of the state was prevented by unobstructed drainage from the melting ice. This modified drift over-laid by till does not therefore appear to bear testimony to a warm interglacial period, or even to any retreat and subsequent.advance of the ce: Emersont reports clay resting upon till in the “ Northamp- ton Lake” deposits. In a few localities he observes till over clay, and, furthermore, explains the contortions of the clay beds by ice moving over them. In the succession of events a minor advance (being the third) of the ice is considered to explain these phenomena. Shaler§ publishes a section at Weewocket, * Report on Geology, Mineralogy, Botany and Zoology of Massachusetts, 1888, 36. + Geology of New Hampshire, iii, 136. t Monograph 29 U. 8. G.S., p. 697. § Bulletin 53 U. S. G. S., p. 16. ft. M. Brown— Clays of the Boston Basin. 449 Nantucket, in which is shown a till deposit over clay. Pro- fessor Shaler at another time,* in summing up the facts of the clays, suggests that they are reconcilable with the supposition that there were several clay-making periods, each marking a retreat of the ice, followed by a readvance. The clays about Boston were studied by Marbut and Woodworth.t Sections of drumlins in Somerville have beeu published by them showing | the clay beneath the till. Professor Woodworth,t in the corre- lation of the deposits along the coast of New England, places the Mystic clays in the second of three glacial epochs. Discussion of Lrelation of Clays to the Glacial Period.— The points that must be explained are as follows: 1. The position of the clays beneath the drumlins in Chelsea and Revere. 2. The considerable amount of clay that makes up a constituent part of the till of the drumlins. 3. The dis- tortion of the clay-beds. Only one conclusion can be reached in regard to the first of these. The clays must have been deposited before the advance of the ice which formed the drumlins. The clayey composition of the drumlins in the neighborhood points to the same con- clusion. In a pit recently opened in the flank of a drumlin situated near Hyde Park, Massachusetts, enough clay was found on the floor to give an aspect of a clay bed. This clay had washed out of the exposed till during the storms, and collected at the bottom of the pit. A little digging exposed a few inches of clay only, and further examination explained the origin of the clay. The per cent of clayey material appears to be too large to be produced by the natural process of grinding, during or just previous to the formation of the drumlins. It seems just, under the circumstances, to presuppose a reservoir of clay from which the drumlins drew their supply. Local advances of the ice have been offered as an explanation for the position of the clay under the drumlins as well as the large percentage of clay in their composition. Emerson considered such an event in the “ Northampton Lake” area. While a local advance of the ice after the last general retreat has been proven along the line of the chain of lakes—Fresh Pond, Spy Pond, the Mystic Lakes, ete.,—it is not consistent to extend this local advance over an area large enough to account for the drumlins of Revere and Chelsea. The local advance would then grow to a general invasion. _ The distortion of the clay-beds offers some additional testi- mony. No explanation has been given for the folding of the clays that has been more satisfactory than the thrust of the *17th Ann. Rep. U.S. G. S., p. 969. 417th Ann. Rep. U.S. G. S., p. 989. +17th Ann. Rep. U.S. G.§S., p. 987. 450 R. M. Brown—Clays of the Boston Basin. advancing ice. The agent of this work has also been con- sidered a local advance, but again the widespread occurrences of these folds indicate the general event rather than a limited one. : Where the surface has been planed off, as in fig. 3, the ice was supplied with its clay, which it deposited in the drumlins of the harbor and the harbor vicinity. The beds must have been developed previous to the ice advance. Upham’s ex- planation, cited above (dated 1883), cannot be considered as applicable for the Boston district, as he demanded a valley slope by means of which the water was held against the side of the glacier so that the warmer water might undermine the edges of the ice. It is not easy to conceive how clays of any amount could be deposited under the ice by such a supposititious theory. There seems to be evidence strong enough to support the belief that some of the clays of the Boston Basin were deposited before the last general advance of the ice; are therefore inter-glacial in origin. New Bedford, Mass. Barbour and Fisher-——Caleite-Sand Crystal. 451 Art. XLIV.— A New Form of Caleite-Sand Crystal; by Erwin H. Barsour and Cassius A. FISHER. UNTIL quite recently the knowledge of calcite-sand crystals was confined to a very few occurrences, that of the well-known “Fontainebleau limestone” being the most important ;* here the erystals are rhombohedral in form (—2R). arene 2 OL BS OSGae" 64°40 35°60 Average of the above -._----------- 63°81 36°19 © Large comeretions.. -- 2... =. 22. Specs 38°12 Sand Clee aingGhew. 0 Ue 63°43 36°57 Average of four radiate sand-lime con- cretions, Sioux County, Nebraska.- 58°89 4111 Crystals from Goshen Hole Region, Wyoming. The new crystals, which also consist of sand cemented by calcite, are very similar in color, texture, and in general appear- ance to those from Washington County, South Dakota, differ from them in being a combination of acute and obtuse "rhom- bohedrons. They show greater uniformity of size, varying but little from one and one-half inthes (40™) in. length, by seven-eighths inch (21™™) in thickness (figs. 3, 4). Apparertly they occur much more sparingly than the others, although the field remains to be fully explored. They show the same tendency to become doubled, clustered, concretionary, and massive to such an extent that descriptions already written of the one kind serve well for the other. If the crystals happen to be particularly small, the size of the sand grains is relatively so large that the exact outline of the * Penfield and Ford, Siliceous Calcites from the Bad Lands, Washington County, South Dakota, this Journal, vol. ix, 1900, pp. 352-4, 1 plate, 4 figures. See also Barbour, Sand-Crystals and their relation to certain concre- tionary forms, presented before the Geol. Soc. of America, Dec. 27, 1900, printed in Bulletin of the Society, vol. xii, pp. 165-172, pls. 13 to 18, April 16, 1901. Barbour and Fisher—Calcite-Sand Crystal. 453 crystal is obscured, and yet to the collector in the field, at least, the identity is plain. The less obvious forms occur in great masses and over wide areas, and pass for concretionary sand. Their extent may be judged better from the fact that they may be traced from the Indian Reservation of South Dakota to northwestern and western Nebraska and eastern Wyoming, as far west, at least, as Bates Hole, which is prac- tically the extent of the Arikaree formation. Without a knowl- edge of the actual sand crystals these obscure forms would ordinarily be unrecognizable. In the case of the new forms as in the case of the older ones they are the result of erystalliza- Fic. 3. Drawing of a crystal showing combination of acute and obtuse rhombohedrons, the theoretical form of the actual crystal shown in figure 4. Fie. 4. Sand-lime crystal, natural size, type found west of Mitchell, in the Chadron sandstone near the North Platte River, on the Wyoming- Nebraska line. tion in a sand bed saturated with water bearing calcium carbo- nate in solution. The lime in erystallizing out followed some one of the forms common to calcite and in the process cemented the sand, together making a sand-calcite crystal. The erystal proper is calcite. The sand may be viewed as an accident incident to the crystallization of lime in a sand bed. A chem- ical analysis shows that those from western Nebraska do not differ essentially from those of South Dakota, as shown by analyses of Mr. Willis Warner (Univ. Nebr. 1901). Analysis of Sand Crystals from Goshen Hole Region. Per cent Per cent of lime of sand. and soluble matter. Baer ebystal = 022 ieee 63°63 36°37 pare GConeretion. 2. 12 2 62°54 37°46 Analyses of the above in full as furnished by Mr. Warner are as follows: Crystal: silica, 49°32 ; phosphorus, ‘011; iron, Fe,O,+Al,0,, 14°21; lime, CaCO,, 33°27 ; magnesia, MeCO,, 3-14; “undeter- mined, probably manganese, "049. 454 Barbour and Fisher—Caleite Sand Crystal. Concretion : silica, 47°94; phosphorus, ‘01 ; iron, Fe,O,+ Al,O,, 14°52; lime, CaCO,, 34:24; magnesia, MeCO,, 3:25; undeter- mined, probably manganese, ‘04. . Distribution and Geologic Range of Sand- Calcite Crystals. The distribution of sand crystals is very wide though they are little known and seldom recognized from the fact that the more obscure forms pass for concretionary sand and receive no attention. ‘They have been personally observed at and around Devil Hill, in the Indian Reservation of South Dakota; in Sioux County, Nebraska; in the North Platte region in Nebraska, at Goshen Hole, "Bates Hole, and inter mediate points . in Wyoming. The larger crystals present no such disparity between the component sand and gravel grains and the crystal itself as do the lesser ones, hence their forms are defined and perfectly apparent. Such forms are restricted and very local in area. Those at Devil Hill occur in enormous quantities along about 100 yards of exposure. The total extent of the bed, which is but a mere remnant of the original, is scarcely one acre. Those from the region of the North Platte river, at or near the Nebraska line, seem to be even more local, and are very scattered in number. The same seems to hold true of those in the Goshen Hole country, which may be classed with the North Platte region, both producing the same crystalline forms shown in figure 4, though differing in horizon. There are but the three above named localities known in this country which pro- duce these crystals. In France, at Fontainebleau, the crystals are similar in physical properties to those from the Great Plains though differing crystallographically, inasmuch as they are simple unmodified rhombohedrons. In vertical range these forms occur in greatest numbers in the Arikaree, though found as low as the Chadron sands at the base of the Oligocene. In the basal sands of the Laramie of Wyoming occur numerous examples of the obscure or concre- tionary type. Locality of sand-calcites. Mica ( Devil Hill, S. D. Tertiary (Arikaree) Sion Coe ae Goshen Hole, Wyoming | Bates Hole, Wyoming Oligocene (Chadron sand) Mitchell region, Nebr. South of Buffalo, Wyoming Cretaceous Laramie Obscure crystals or concre- tionary sand University of Nebraska, Lincoln, Nebr. Chemistry and Physics. 455 SCIENTIFIC INTELLIGENCE. I. CHEMISTRY AND PHysIcs. 1. Transformation of Carbon into Diamond.—It was sbown by Pepys, in 1815, that an iron wire heated to redness in contact with diamond was converted into steel. Dr. ALBERT Lupwic now claims that under great pressure in an atmosphere of hydrogen this reaction is reversed, and also that carbon fused in the electric are in absence of iron, under the same conditions of pressure, is likewise converted into diamond. In carrying out the experi- ments, pressures as high as 3100 atmospheres were used. A spiral of iron wire was embedded in powdered retort-carbon and heated by an electric current in a highly compressed atmosphere of hydrogen. In afew moments the resistance, which was slight at first on account of the conductivity of the carbon, rose to that of the iron spiral. This indicated that the carbon in contact with the spiral had become non-conducting, and careful examination showed that on some of the pieces of carbon were br illiant, minute crystals, possessing the hardness, specific gravity, and refraction of the diamond. The greater part of the carbon contained in the iron spiral had also been converted into diamond. The crystals had the characteristic irregular surface shown by the diamonds _ produced by Moissan by the sudden cooling of molten iron. To produce diamonds without the use of iron, it was found necessary to use much higher temperatures and actually fuse the carbon under very high pressure. Thus fused it was shown to be a non- conductor, and hence was considered to be molten diamond. Under the pressure employed this fusion took place very easily in the electric arc, and there were thus obtained spherical masses, of the size of peas, having the great hardness and crystalline structure of carbonado. It is the intention of the author to develop the process for the commercial manufacture of diamonds. — Chemik. Zeitg., xxv, 979. H. L. W. 2. An Lodometric Titration of Thiocyanie Acid. —It has been shown by Rupp and Schied that sulphocyanides are oxidized in sodium bicarbonate solution, according to the equation, HSCN +41,+4H,O=H,S0,+7HI+CNI, but starch cannot be used as an indicator in applying this reaction on account of the presence of cyanogen iodide ; and, moreover, the yellow color of the latter compound makes the method applicable only to small quantities where the disappearance of the iodine color is used. I[t has been found by Meinecke, however, that in acid solutions the following reaction takes place: CNI+ HI=I,+ HCN. Tuite has now used the facts which have been stated for devising a very convenient method for making this titration. The thiocyanate is first treated with an excess of iodine solution in the presence of sodium bicarbonate, enough water being used to dissolve the latter. The reaction is complete in four hours at 456 Sctentijic Intelligence. ordinary temperature. Then an excess of hydrochloric acid is. added, and the excess of iodine is determined at once by means of sodium thiosulphate solution, with the use of starch as an indica- tor. The final result corresponds to the equation, HSCN +-3],+4H,O=H,SO,+6HI+HOCN. The experimental results obtained were extremely accurate, and the author advises the standardization of volumetric thio- cyanate solutions by this method.— Berichte, xxxv, 2766. H.L. w. 3. Lodine Pentafluoride.—This compound was prepared, pro- bably in an impure condition, by Gore in 1871 and by Maclvor in 1875, by the action of iodine upon silver fluoride. Morssaw has now prepared it by allowing fluorine gas to act upon iodine. Combination takes place with evolution of heat and the product is a colorless liquid boiling without decomposition at 97°, and solidifying at 8°. In the solid state it resembles camphor. The liquid fumes in the air, and when poured into water it is decom- posed without violence into hydrofluoric and iodic acids accord- ing to the equation, ' 21K, +5H,O = 1,0,+10HF. The fluoride possesses great chemical activity ; most elementary bodies decompose it, and it enters into reactions with a great number of compound substances. When its vapor is heated to the neighborhood of 500° it decomposes, showing the color of iodine vapor.— Comptes Rendus, cxxxv, 563. H. L. W. 4, Separation of Manganese from Magnesium, Zine and Aluminum.—To effect these separations DieTricnw and HassEn precipitate the manganese as higher oxide in dilute sulphuric or nitric acid solution by means of ammonium persulphate. For quantities of manganese corresponding usually to -1¢ MnO or less they used 5°¢ of dilute sulphuric acid (1:10) and 15—20° of a ten per cent solution of ammonium persulphate. In the separa- tion from magnesium the total volume of the liquid was 150-200°, while in the other cases, where the quantities of zine and alu- minum oxides present were about the same as that of the man- ganese Oxide, a volume of 400-500°° was used. The precipita- tions were made in solutions heated upon the water-bath and frequently stirred, and the heating was continued for about two hours in order to decompose the excess of ammonium persulphate. The manganese precipitates, after filtering and washing, were ignited directly, and Mn,O, was weighed. The test analyses gave very satisfactory results. It seems probable that this method will find useful application in mineral and rock analyses, in which, by the usual methods, the separation especially of man- ganese and aluminum presents some difficulties.— Berichte, xxxv, 32662" 2% B.D we 5. Plasticity and Adhesiveness of Glass at Ordinary Tem- peratures.—That glass possesses a certain amount of plasticity when not heated has been known for a long time, but it has not been shown definitely that this plasticity is sufficient to produce adhesion similar to the welding of metals. Piccarp has now eee ES ee ee eee Chemistry and Physics. 457 made experiments which indicate that the thin cracks extending from ‘05 to :1™™ below the scratch made by the glass-cutting diamond may be healed to a considerable extent in from one to three days by gentle pressure. The experiments were conducted by comparing the loads required to fracture freshly scratched pieces of glass and those which had been slightly bent for several days in such a way as to press together the ruptured surfaces. — Berichte, xxxiv, 3635. BEE Welt 4 6. General Principles of Physical Science; by Artuur A. ~ Noyes. 8vo, pp. 172. New York, 1902 (Henry Holt & Co.).— The purpose of this volume is to present the principles and laws of physics and chemistry which lie at the basis of the modern science of theoretical chemistry. The treatment is non-mathemati- cal toa greatextent. Thetwo main chapters of the book treat respec- tively of the general principles relating to matter and to energy. The book forms the first part of a work on the general princi- ples of chemistry, which has had to be discontinued. It is to be hoped that Professor Noyes will continue the work in the future. H. W. F. 7. Lehrbuch der Allgemeinen Chemie ; by Dr. Wi~HE Lm Ost- WALD. 2 vols. Leipzig, 1902 (Engelmann).—The last section of the second part of volume ii has just appeared. A third part is to appear in the future. This work is by far the most compre- hensive which has yet appeared in the field of physical chemistry and probably comes as near treating the whole subject as it is possible to do. It is to be regretted that volume i and the first part of volume 1i are already out of print. H. W. F. 8. The Spectra of Hydrogen and Reversed Lines in the Spectra of Gases ; communicated by Joun TrowpripGr.—In a previous paper* I described the spectra produced by powerful condenser discharges through Geissler tubes filled with hydrogen. A fairly continuous spectrum was obtained between the HH lines and the red end of the spectrum which was traversed by reversed lines. In that paper I expressed the hope of being able to obtain quartz tubes. This hope has been realized. Through the kindness of manufacturerst working under the direction and according to the method of Professor Shenstone of Clifton College, England, I have obtained suitable tubes, and the results given by such tubes are so remarkable that they seem worthy of a preliminary paper. The tubes are eight centimeters in length ; with a capillary four centimeters in length and about two millimeters in diam- eter. On account of the difficulty of inserting platinum termi- nals in quartz, I had the ends of the tubes ground smooth ; and the glass blower of the laboratory prepared glass bulbs in which suitable electrodes were inserted. These bulbs were luted to the ends of the quartz tubes. In certain cases where metal plates were luted directly to the ends of the quartz tubes I employed silicate of soda as a luting agent ; and after this had hardened I applied on the outside of the joint a hard preparation of pitch and shellac. The glass bulbs were covered with other bulbs which allowed * This Journal, vol. xiv, p. 1. + Baird and Tatlock, London. 458 Scientific Intelligence. a current of water to circulate from the upper end of the tube to the lower. The great heat, however, was excited in the capil- lary of the tube. Quartz prepared by the method of Professor Shenstone possesses the property of resisting changes of tem- perature in a remarkable manner. One of these quartz tubes can be heated to a white heat and plunged into water without crack- ing. Such tubes, therefore, are very valuable for the experiments I have been conducting on gases at high temperature. They also possess the great advantage over end-on tubes of glass provided with quartz window, that the capillary can be placed close to the slit of the spectroscope ; thus giving a very intense light and a broad spectrum. Moreover, the quartz is not melted by the intense heat. A photograph of gaseous spectra can be obtained with a single discharge and a very narrow slit ; with tubes filled with hydrogen excited by a difference of poten- tial of twenty thousand volts, condenser ‘3 microfarads, an extremely intense light is obtained. This light is dazzling white with a bluish cast. It has more than three times the actinic effect of the same quantity of electricity discharged between magnesium terminals. Viewed with a strait vision spectroscope, the spectrum appears continuous, and even photography fails to reveal bright lines between the HH lines and the red end of the spectrum. In the region, however, beyond the limit set by the absorption of the glass Geissler tubes there are both bright lines and dark lines. The principal reversed lines are at wave lengths 2889°70 ; 2549°89; 2528°60; 2524°29 ; 2519°3 5; 2516°21. These lines correspond with the lines of silicon volatilized by the spark in air. It seems that we have in this phenomenon another instance of selective solarization mentioned in my pre- vious paper. The strongest metallic lines or gaseous lines are not those which show the strongest reversal. For instance, the cal- cium line at approximately 4227 is strongly reversed, while the stronger 3968, 3933 do not show a reversal, except with much stronger and longer continued discharges. A careful inspection of the negatives shows that the reversals of the metallic lines occur when they fall on bright gaseous lines or bands. In the same way a bright gaseous line falling on a continuous spectrum can show a similar reversal. We can express this in symbolic language as follows: let A represent the intensity of the line and B the amount of the previous action of light on the photographic plate, then the reversal appears to be proportional to AB. It seems probable that there are similar reversed lines running through the solar spectrum and I hope to detect them. This investigation shows that the presence of dark lines in the spectra of stars does not imply necessarily the presence of revers- ing layers of a colder state of the gases; for such reversal may arise from photographic action on the plates which are used. Moreover a gas may show a continuous spectrum to the eye, or even when photography is employed with glass tubes and glass lenses; while with quartz tubes such as I have employed a large Chemastry and Physics. — 459 region in the ultra violet is shown to be traversed by both dark — and bright lines and bands. Jefferson Physical Laboratory, Harvard University. 9. A New Holtz Machine.—The influence electrical machine in many respects has been found to excel the induction coil for the excitation of X-ray tubes. H. WommeEtsporr describes a new electrical machine which he calls the condenser machine. It con- sists of many discs similar to those now used in the Holtz machine. ‘There is a large condenser action between the glass plates which are provided with suitable sectors. We have thus a row of condensers; one set of plates or coated layer remaining fixed while the intervening plates revolve. A small model, 30™ high, 28° long and with a breadth of 22, affords a larger quantity of electricity than the largest Holtz machine, and this new machine promises to be of the oreatest use in the excitation of X- -Tay tubes. — Ann. der Physik, No. 11, 1902, pp. 651-659. Lega, 10. Hlectrical Conductibility of Metals and their Vupors.— Hon. R. J. Strutt finds that (1) Mercury vapor is an insulator, while liquid mercury is a conductor. Since the liquid and satu- rated vapor are indistinguishable above the critical temperature, one or both of these must undergo a remarkable change of elec- trical properties as that temperature is approached. (2) Attempts to predict the critical temperature of mercury seem to lead to results altogether inconsistent with one another. (3) Attempts to observe the critical temperature of mercury and arsenic in quartz tubes have failed. In both cases experi- ment proves that the critical temperature lies above a dull yellow heat. (4) Up to a full red heat the conductivity of saturated mer- cury vapor remains of quite a different order of magnitude from that of the liquid, the latter being ten million (10’) times as great as the former. But on the other hand, the conductivity of the saturated vapor is immensely greater than that of the vapor at atmospheric pressure. For the former was found to have a resistance of 10’ times that of the liquid, the latter more than 410" that of the liquid. Thus the vapor at atmospheric pres- sure has a resistance about 4X10’ times that of the saturated vapor, both at a full red heat. It need scarcely be said that this ratio is of quite a different order from the ratio of the densities of those vapors. It seems likely that as the critical temperature is approached the vapor begins to conduct freely, while the liquid changes its electrical character to a much less extent. (5) The conductivity of saturated arsenic vapor at a bright red heat is of the same order as that of mercury, and obeys Ohm’s law, at all events up to an electromotive intensity of more than 100 volts per em.— Phil. Mag., Nov., 1902, pp. 596-605. J. 7. 11. Lonization of Nuclei Produced by Violent Agitation of Dilute Solutions ; communicated by C. Barus.—Discharging the nuclei produced by violent agitation of dilute solutions, in a steady stream at once into a tubular condenser, the following deflections 460 Scientific Intelligence. of the electrometer (with very light needle) were observed at intervals of half a minute: Charge+, 14:4, 10°5, 6°5, 3-4; time rate 7°5. Charge—, 21°5, 20°0, 18:2, 16°2, 14°2, 12°2; time rate 4°0. Charge+, 18°3, 14:5, 10°4, 6°7, 3°3, °9; time rate 7°6. The surprising result is thus obtained that the electric current is con- stant while the initial charge of the inner coating of the con denser (the outer being earthed), at nearly 20 volts, gradually quite vanishes. In explanation it may be assumed either that the number of ionized nuclei at constant ionic velocity varies inversely as the potential difference, or far more simply, it seems to me, that the velocity of the nuclei is independent of the potential gradient, each nucleus retaining its own specific velocity in the presence or the absence of an electric field, while the number of nuclei is appreciably constant—the point of view taken in my earlier work (Smithsonian Contributions, 1901). The difference of current for positive and negative charges follows from the known excess of negative nuclei. The initial ionization is of the same order as that of the phosphorus emanation. 12. Handbuch der Spectroscopie ; by H. Kayser. Vol. 11, 698 pp., 4 tables, 57 figs. (Leipzig, S. Hirzel) —The appearance of the second volume of this work gives further assurance of the thorough treatment of the whole subject of spectroscopy which we may expect from this eminent worker in the field. In the present volume, the first chapter is devoted to emission and absorption, with the history, development and proofs of Kir- choff’s law. The chapter on radiation of solids furnishes an exhaustive discussion of the various laws which have been formu- lated connecting the emission with the absolute temperature, the distribution of the energy in the spectrum, and the attempts to apply the results in the measurement of temperature. Under radiation of gases, the sources of energy and the production of ether vibrations in general are discussed. This is followed by a detailed treatment of the spectra of compounds and of the differ- ent spectra given by the same substance under varying con- ditions. The succeeding chapters deal, respectively, with the influence of pressure, temperature and the nature of the electric discharge upon spectra; the appearance of spectral lines, their broadening, and reversal ; Doppler’s principle and its applications, in the discussion of which the author has been assisted by Dr. H. Konen ; the general relations which have been discovered among the lines of the spectra of individual elements and of those af Mendeleeff’s groups. The concluding chapter brings up to date the work which has been done upon the vibrations of light in the magnetic field. Prof. C. Runge has assisted in the development of the Zeeman-effect in accordance with the modern ionic theory. Evidently no effort has been spared in making the references to the literature of every subject discussed as complete as possi- ble up to 1901. The volume is replete with suggested problems of research, to stimulate which is one of the purposes which the author hopes the book may serve. D, Ans Geology and Natural History. 461 II. Guotocy anp Narurat History. 1. United States Geological Survey.—The following publica- tions have been received : Minera Resources oF THE UNITED STATES FOR THE CAL- ENDAR YEAR 1901; by Davin T. Day. 973 pp.—For the second time the annual mineral production exceeds $1,000,000,000. The important metals except iron and zinc have decreased in output and value. 1,408 ounces of platinum were produced in 1901 compared with 400 in 1900. Building materials, clays and abra- sions show greatly increased production. For the first time in the United States arsenious oxide was manufactured at Seattle, and rutile was produced on a large scale—in Nelson Co., Va. Buuietin No. 195.—Structural details in the Green Mountain Region and in Eastern New York; by T. Netson Date. 10 pp., 4 pls., 8 figs. Some interesting examples of structures in meta- morphic rocks are described and well illustrated. These details have been collected since the publication of Professor Dale’s previous papers on this region (16th Ann. Rept., Pt. I, pp. 549- 570, 19th Ann. Rept., Pt. ILI, pp. 199-217). Bu.uetTin No. 203.—Bibliography and Index of North Ameri- can Geology, Paleontology, Petrology and Mineralogy for 1901 ; by F. B. WrEExs. 144 pp. 2. Geological Survey of Kansas—Special Report on Mineral Waters ; by EK. H. 8S. Batrzy. Vol. vii, pp. 25-333, 38 pls.— Kansas is well supplied with marketable mineral waters. Mr. Bailey describes and gives the analyses of some 87 springs and wells separated into groups according to their mineral content. _ He also discusses the medicinal value of the various waters and the industrial uses of the brines. Dr. W. R. Crane contributes a chapter (pp. 323-333) on the Geological Distribution of mineral springs and wells. } ‘ 3. A Quantitative Chemico-mineralogical Classification and ' Nomenclature of Igneous Rocks ; by Wuirman Cross, J. P. Ipp- ines, L. V. Pirsson and H. 8. Wasurneaton (Jour. of Geol., vol. x, No. 6, pp. 555-690, 1902).—In this work is presented an entirely new system for the classification and nomenclature of igneous rocks, a result which the authors believe is to be best attained by the codperation of several workers agreeing on funda- ‘mental principles. Originally the late Prof. G. H. Williams was also one: of the collaborators. : The authors state that after many attempts to modify and use existing systems this was perceived to be impossible if one should evolve at the same time a comprehensive and rational one based on recent investigations and knowledge. Thus through repeated trials the present system was gradually worked out, and with its evolution has gone hand in hand the calculation of thousands of analyses by which it has been tested and its formation in part controlled. It is a chemico-mineralogical system based on its own principles, and as its concepts of rocks are in great bart new it demands a new momicnelatuie, 462 Scientific Intelligence. What the authors propose is as follows: All igneous rocks are classified on the basis of their chemical composition ; all rocks having like chemical composition are grouped together. | The definition of the chemical composition of a rock and of a unit of classification is expressed in terms of certain minerals capable of crystallizing from a magma of a given chemical com- position, and the expression is guantitative. For this purpose the rock-making minerals are divided into two groups, the one of the more siliceous alkali-and calcic-aluminous ones, the other of the ferro-magnesian minerals. The first group is called mnemonically the salic group; the second one, the femic group. From this category the aluminous augites and amphiboles and the micas are excluded for reasons given. To completely classify a rock by this system its chemical com- position must be known by chemical analysis or approximately so by physical or microscopic optical methods indicated by the authors. Rocks once determined become types by which similar rocks may be approximately classified. , Since a given magma may crystallize into quite different min- eral combinations according to the different conditions attending its solidification, it is necessary to select a certain set of salic and femic minerals as uniform standards of comparison, These are the ones ordinarily formed, but aluminous augite and hornblende - and micas are excluded. In practice, the molecular composition of a rock obtained from its chemical composition (determined as mentioned above) is computed into amounts of these standard minerals and its place in the system is then easily determined. The standard mineral composition of a rock is called its norm, and this may be quite different from its actual mineral composi- tion or mode. Methods are given for obtaining the latter and indicating its relation to the former. On the relative proportions of these two groups of standard minerals the rocks are divided into five Classes, accordingly as one or the other of these two groups alone constitutes the norm or is extremely abundant ; whether one or the other is dominant ; or whether the two are present in about egual proportions. These Classes are then divided into Orders on the relative proportions of the minerals forming the predominant group in each case and in the middle group on the relative proportion of the salic min- erals. So in the preponderantly salic classes the orders are based on the relative proportions of quartz, feldspars and feldspathoids. The Orders are divided into Jtangs on the chemical character of the basic oxides in the minerals in the preponderant group in each case; thus if these were feldspathic, as to whether they are alkalic, alkali-calcie or calcic. The lowest division or grad obtains only in the three intermediate classes and results from the con- sideration of the relative amounts of the minerals forming the subordinate group in each case. Where necessary there are sub- classes, suborders, subrangs and subgrads. Texture is considered of minor importance and is taken into account after the chemical and mineral composition. Geology and Natural History. 463 Nomenclature. ‘The system demands a new nomenclature and this has been provided for according to a definite system. As proposed it consists of three parts, substantive names for the mag- matic units, implying the chemical composition and the norm ; then two sets of adjective terms to qualify these nouns, one referring to the mode and the other to the texture. The magmatic name consists of a root, geographical in all cases except for the names of the five classes, and of a suffix. The suf- fixes are chosen so that they vary in a definite way with the division of the system to which the magmatic name belongs. Thus for Class, Order, Rang and Grad, the letters n, 7, s and ¢ in alphabetical order are used with the vowel a, giving in English ane, are, ase, ate. For subclass, suborder, etc., the vowel is 0, giving one, ore, ose and ote. In the geographical roots, so far as possible those in present use are retained, advantage being taken of their connotation as to magmatic character. The authors propose a nomenclature for field use based on purely megascopic characters. The work concludes with a discussion of methods of calculat- ing mineral composition from chemical composition and the reverse, and presents tables to aid such calculations. 1. V. P. 4, Petrography and Geology of the Monzoni region in Tyrol. —The exhaustive study of this area, so long known and so much investigated as to be perhaps rightly called a classic one, has recently received a new impetus, apparently from the suggestive work of Brogger (ii Die Eruptionsfolge der triadischen Eruptiv- gesteine bei Predazzo in Siidtirol). A number of shorter articles by various authors have appeared describing new types of rocks or various phases of its geology. Quite recently, however, more important memoirs on the geology and petrography of the region, the one by Rompere (Geologisch—petrographische Studien im Gebiete von Predazzo 1 and i, (Sitzber. d. K. preuss. Akad. d. Wiss. Berlin, 1902, phys. mat. class. 675), the other by DoELTER (Tscher. Min. and Petro. Mitt., vol. xxi) have been published. The various authors have not entirely agreed among themselves regarding various points and this has led to a stimulation of in- terest in their work. As a result many new analyses and descrip- tions of important rock types have been given. It is shown that the forecast of RoszeNsBuscu on theoretical grounds, regarding the existence of nephelinitic and other alkaline types, was correct, and in general a considerable amount of new information, of value to systematic petrography, has been developed by these excellent studies. hia Vo 5. Gesteinskunde fiir Techniker, Bergingenieure etc., von F. RinNE. (8°, 206 pp., 4 pls., 235 figs. Geb. Jinecke.) Hanover, 1901. —In this excellent and well written little volume is given a general survey of the subject of petrology from the modern standpoint, with especial reference to its use by beginners and those desiring some knowledge of the subject for technical purposes. It is also a good introduction to the science for workers in other fields in Am. Jour. Sci.—Fourts SERIES, Vou. XIV, No. 84.—DxEcremBer, 1902. 32 464 Scientific Intelligence. geology. Some optical mineralogy is introduced and the use of the microscope indicated. A further advantage is that a con- siderable amount of physical geology, in so far as it relates to the subject, is brought in. NS cal Srere 20 ES) E20 1 99°75 99°15 99°58 — Geol. Surv. W. Australia, Bull. No. 6, p. 18. CoLORADOITE occurs freely and in large pure masses at Kal- goorlie. A new analysis of pure material is of interest: Hg, 50°40; Au, trace; Ag, 12; Te, 49°48; total, 100-00. Specific gravity, 9°21. The formula for coloradoite calculated from these figures is Hg, Te,, requiring : Hg, 51°7 per cent.; Te 48°3 per cent. The pre- viously accepted formula based upon analysis of small and impure specimens was HgTe, requiring: Hg, 61°6 per cent.; Te, 38°4 per cent.— Geol. Sur. W. Australia, Bull. No. 6, p. 27. 466 Scientific Intelligence. STIBIOTANTALITE, a tantalo-niobate of antimony, Sb(Ta,Nb)O4 is found in the stream works at Greenbushes. The exact crystal- line form of the mineral has not been determined for it occurs in water-worn pebbles with a very smooth bright surface. It is brittle, with a subconchoidal to granular or occasionally fibrous fracture. Its hardness is 5 to 5°5, and specific gravity 6°4 to 7°4. Its luster is adamantine to resinous ; color, various shades of yel- low and brown, also gray. It is subtranslucent to opaque. Its composition is shown by the following analysis by Goyder: Sb,O,, 40°23 ; Bi,O,, 82; NiO, -08; Ta,O,, 51:13 ; Nb,O,, 7°56 ; total, 99°82. A hydrated variety of this mineral occurs also, resembling it in color, but having a rough surface. Its formula would appear to be 2Sb(Ta,Nb)O4:7H,O. Before the blowpipe stibiotantalite is practically infusible and colors the flame greenish-gray. It is reduced to metallic antimony by fusion with potassium cyanide. In the closed tube the anhydrous mineral gives no sublimate ; the hydrous, a sublimate of water. After mixing with sulphur it gives in the closed tube a sublimate which is black when hot and brownish red on cooling. It is soluble in hydrofluoric acid ; this solution on adding a little potassium fluoride and evaporating somewhat, deposits on cooling a felt-like mass of colorless crystals of potassium fluotantalite. If some of the solution in hydro- fluoric acid be poured into a platinum dish and a piece of pure zinc be dropped into it, a black stain immediately develops on the plate. Stibiotantalite is decomposed by fusion with potas- sium bisulphate.— Geol. Sur. W. Australia, Bull. No. 6, p. 42. HIsTRIXITE, an apparently new sulphide of antimony and bis- muth, is described by W. F. Pretrerp. It occurs in radiating groups of crystals which are orthorhombic, with acute but indis- tinct terminations and are striated longitudinally. It is slightly sectile with a hardness of about 2. Luster eminently metallic. Color and streak, steel-gray. The mean of two analyses is :— S, 23°53; Bi, 56°00; Sb, 9°70; Cu, 6°49; Fe, 5°31; total, 101-03. which gives for the formula, 7Bi,S,,2Sb,8,,5CuFeS,.—John Vail, Gov. Printer, Tasmania. PETTERDITE, a new oxychloride of lead. This mineral, which was found at Zeehan, Tasmania, was described by Mr. W. H. TweELveTrees. It occurs in thin hexagonal plates of a white color. Fracture is irregular, luster dull, hardness 1°5 to 2, specific gravity 7:16. The analysis made by Mr. O. E. White of Hobart is as follows :—PbO, 74:04; As,O,, 2°60; P,O,, 2°10 ; Sb,O,, -50; Cl, 20:00; total, 99:24.—John Vail, Gov. Printer, Tasmania. w.. F. 8. Gold in Meteorites—At the September meeting of the Royal Society of New South Wales, Prof. LiversipeE exhibited under the microscope particles of a malleable yellow metal, insol- uble in nitric acid, which have all the appearance of gold obtained from certain Australian and European meteorites (siderolites). The presence of gold in meteorites bears upon the presence of gold in “meteoric” dusts, and it is also of great interest in con- nection with the presence of gold upon the earth and in sea-water, Geology and Natural History. 467 inasmuch as meteorites and the dust of meteorites are constantly falling upon the earth, to the extent of probably many million tons a year. Further information upon the question of the pres- ence of gold in meteorites is promised in a subsequent paper. 9. Triassic Ichthyopterygia from California and Nevada ; by Joun C. Merriam. Bulletin of the Dept. of Geol., Univ. of Cal., vol. ii, No. 4, pp. 63-108, pls. 5-18.—A valuable contribu- tion to Paleontology, based chiefly upon saurian material from the upper Triassic of Shasta County, California, collected in 1891 by field parties from Stanford and California universities. | The great value of the monograph under review lies in the carefully executed plates and in the accurate measurement and description of the bones of a hitherto little known group of extinct reptiles. Collectively, the several specimens described afford an excellent generic definition of Shastasaurus, the anterior part of the skull and the distal ends of the paddles being practi- cally the only portions of the skeleton which now remain unknown. Prof. Merriam has met with the great, though by no means rare, good fortune to find in his collected material nearly as many species of Shastasaurus as individuals, seven examples offering more or less complete descriptions of five new forms, S. perrini, osmonti, alexandra, careyi, and altispinus, although none of the new acquisitions have been identified with the type species S. pacificus, which was described by him in 1895 (this Journal, vol. iv, p. 56). The type species is shown to differ from S. per- rint in regard to certain posterior dorsal vertebrez and the pubis. None of the other new species, however, are represented by these parts, and therefore cannot well be differentiated from the type. The author wisely states: “ At the present time we cannot deter- mine definitely the relations of pacificus to the better known Species, and it is not impossible that when the other parts of the skeleton of those forms are better known it will be found that some one of them should be included in pacificus.” In view of this lack of comparison and the urgent need of simplicity, the doubt naturally arises whether the purpose of classification would not have been better served by uniting, provisionally at least, one of the new forms with the type species. Accompanying the discussion of Shastasaurus is a careful revision of Leidy’s genus Cymbaspondylus from the middle Tri- assic of Nevada, which is shown to be closely related to Shasta- saurus. The family Shastasauride is proposed to embrace these two genera, distinguished as they are from the Mixosauride, Ichthyosauridex, and Baptanodontide, by the peculiar articulation of their dorsal ribs, the form of the pelvic girdle, and their long- spined chevron bones. In a postscript, Prof. Merriam states that a good collection of saurian material has just been obtained from the middle Triassic of Nevada. When these specimens have been properly worked out, another contribution is promised by the author. This will be awaited with great interest, and it is confi- dently hoped that further investigation will yield as satisfactory results as the monograph before us. G. F. E. 468 Scientific Intelligence. 10. Zoological Results based on material from New Britain, New Guinea, Loyalty Islands and elsewhere, collected during the years 1895, 1896, 1897; by Arraur Wittey. Part VI (August, 1902), pp. 691-826, 8 pls., 33 figs—Dr. Willey is to be congratulated upon the completion*® of a valuable series of zoolog- ical papers. The present volume contains the results of a study of the development of the Pearly Nautilus. The interesting “ per- sonal narrative” (pp. 691-734) is illustrated by photographs of the natives who carry on the Nautilus-fisheries on the different islands, and who came in contact with Mr. Willey during his visits to the ar chipelago (1894 and 1897) in search for the eggs of species of Nautilus. The “special contribution” (pp. 736-826) is prefaced by a complete review of the bibliography of nautilus since the first description with figures of the external characters by Rumphius, 1705, and of the animal by Bennett, 1831. Many new and interesting facts are mentioned. It was found by obser- vation that the color markings on both the shell and animal “exerted a protective influence”; that the “wart—like gibbos- ities” on the upper surface of the hood form a shield for pro- tecting the aperture of the shell when the animal is in retraction, aud not a foot for locomotion. The studies of the anatomical characters show the relation of the Vautilus to the dibranchs, but with reference to the other cephalopods opinions will differ. It is, however, one whose external shell is probably primitive as compared with the internal shell of Spirula. No definite opinion is given as to whether the many similarities in anatomy between the Nautilus and diotocard prosobranchs (Haliotis, Fissurella and Pleurotomaria) are of the nature of affinity or convergence, but an interesting figure (15) is given showing a shell with a median groove and shell-slit similar to Pleurotomaria. XK. J. B. III. MiIsceELLANEOUS SCIENTIFIC INTELLIGENCE. 1. National Academy of Sciences—The following is a list of papers read before the National Academy at the meeting in Baltimore, Nov. 11-12. S. L. PenrreLp: A possible explanation of the difficult solubility of cer- tain compounds containing fluorine and hydroxyl. GrorGE E. Hate: The spectra of stars of Secchi’s fourth type. T. C. MENDENHALL: Biographical memoir of Henry A. Rowland. W. K. Brooxs: The embryology of Salpa cordiformis. CASWELL GRAVE: The occurrence of reef corals near Beaufort, N. C. D. H. Tennent: The Trematode parasites of the oyster. H. N. Morse: The preparation of cells for the measurement of osmotic pressure. R. W. Woop: A substance with remarkable optical properties, and screens transparent only to ultra-violet light. J. B. WHITEHEAD: On displacement currents. L. A. Parsons: On the spectrum of hydrogen. Lewis Boss: A new system of positions for standard stars, with notes relative to its bearing upon sidereal astronomy. H. F. Ossorn: Complete skeleton and restoration of the Cretaceous fish Portheus molossus Cope. A new small dinosaur from the Jurassic or Como * See this Journal, vii, 79, 322; viii, 398; x, 89; xi, 330. Miscellaneous Intelligence. 469 beds of Wyoming, apparently a bird-catcher. New or little-known elephants and mastodons of North America. A. Acassiz: On elevated Oceanic Islands in the Pacific. 2. American Association for the Advancement of Science.— The next meeting will be held in Washington, Dec. 29 to Jan. 3, inclusive. ‘This is the first time the Association has met in the winter. | 3. Smithsonian Institution, Annual Report for 1901; by S. P. Lanewey, Secretary. Pp. lvii+ 739, 71 pls.—The last report of the Smithsonian Institution shows that increased appropria- tions means increased volume of important work. Fifty articles by well known specialists tell of the latest progress in the princi- pal branches of knowledge. . 4. United States National Museum. Bull. 51,168 pp. List or PusiicaTIons 1875-1900, by Ranpo.tpu I. Geare.—The National Museum has issued a complete list of its publications, arranged both asa chronological record and as a subject and title index. 5. British Museum — Catalogue of the Collection of Birds’ Figgs ; by Evcene W. Oares. Vol. ii, 400 pp., 15 colored plates. —Descriptions are given of 15,000 specimens of eggs belonging to the Carinate. Ten orders and 726 species are included in the list. : 6. United States Coast and Geodetic Survey ; O. H. Tirrman, Superintendent : ANNUAL Report 1901. 423 pp., 46 illustrations, 4 maps in pocket.—The superintendent of the Coast Survey reports the inauguration of the survey of the Philippine coast line and the establishment of a suboffice for the publication of charts and notices to mariners. Parties were also at work in Porto Rico, the Hawaiian Islands and Alaska. Perhaps the most import- ant field work now in hand is the measurement of the 98th meridian. Mr. A. L. Batpwin reports on the Measurement of Nine Bases along the 98th Meridian (pp. 241-302); and Mr. J. F. Hayrorp, inspector of geodetic work, describes the present state of the triangulation along this meridian in Kansas and Nebraska. The measured are will cover 23° of latitude within the United States; the Mexican government is expected to extend it 9° southward, and it is possible to extend it far northward. THe Eastern Opsriquze Arc oF THE UNITED STATES AND OscULATING SPHEROID ; by Cuas. A. Scuotr. Special Publication No. 7, 394 pp., 38 illustrations, 2 maps in pocket.—The second long are measured by the Coast Survey extends from Calais, Maine, to New Orleans, La. The line is 2612°3 kilometers in length, covering 23° 30’ 57”, and is unigue in that it is the first one which utilizes on a grand scale a measurement oblique to the meridian. The work was begun in 1833 and the field work finished in 1898. The Eastern Oblique Are intersects the Transcontinental Are of the 39th parallel in Maryland and Virginia. With the measure- ments along the 98th meridian well under way and two long ares already completed, the Coast Survey may well feel proud of its contributions to geodesy. 470 Scientific Intelligence. 7. United States Naval Observatory, Captain C. H. Davis, U. S. N. Superintendent. Publications, Second Series, Vol. II. Zonz OBSERVATION WITH THE N1INE-1NcH Transit CrrcLE, 1894-1901; by Aaron N. SKINNER, assisted by Franx B. Lirrett and THeo. I. Kine. pp. xxviii, 525. is volume embodies the results of observations made, in accordance with the suggestion of Dr. A, Auwers of the Astronomische Gesellschaft, on stars to the ninth magnitude, inclusive, between the parallels, —13° 50’ and —18° ae 8. Bureau of American Ethnology.—The following volumes have recently come to hand: NINETEENTH ANNUAL Report; by J. W. Powett, Director. Pt. L, pp. xcii+548. 79 pls., 48 figs. An exhaustive report on the Myths of the Cherokee Indians has been prepared by James Mooney, (pp. 3-548). Buiietin No. 26—Kartuiamet Texts: by Franz Boas. 261 p., 1 pl. i 9. Ostwald’s Klassiker der Exakten Wissenschaften. Leipsig, 1902 (Wilhelm Engelmann).—The following are recent additions to this valuable series : Nr.-129. Allgemeine Methode partielle Differential gleichungen zu inte- griren ; von Johann Friedrick Pfaff. Pp. 84. Nr. 130. Pangeometrie ; von N. J. Lobatschefskij (Kasan 1856). Pp. 95. Nr. 131. Experimental-Untersuchungen uber Elektricitét (xiv und xv Reihe) ; von Michael Faraday (London 1838). Pp. 48. Nr. 132. Uber die Continuitat der gas formigen und fltissigen Zustande der Materie, und Uber den gas férmigen Zustand der Materie; von Thomas Andrews (London 1869). Pp. 81. Nr. 193. 3. Ranberhsl Abhandlungen zur Bahnbestimmung der Come- ten, Pp. 148. 10. Hodgkins Gold Medal Awarded.—The second Hodgkins Gold Medal has been awarded -to J. J. Thomson of Cambridge, England, “for his investigations on the conductivity of gases, especially on the gases that compose the atmospheric air.” The committee of award consisted of Mr. Richard Rathbun, Chair- n; Doctor A. Graham Bell, for Electricity ; Doctor Ira Rem-. sen, for Chemistry ; Doctor Charles D. Walcott, for Geology ; Professor E. C. Pickering, for Astronomy ; Doctor Theodore N. Gill, for Biology ; Professor Cleveland Abbe, for Meteorology ; Mr. William H. Holmes, for Anthropology, and Mr. S. W. Strat- ton, for Physics. OBITUARY. Dr. OaprEN Nicnoxas Roop, Professor of Physics in Columbia University, died November 12 at the age of 71. (A sketch of the life and work of Professor Rood will appear in this Journal for January.) Dr. Rosert C. Kenzie, for forty years Professor of Chemistry at the Michigan Agricultural College, died November 7, at the age of 79 years. Dr. Rozert Rusenson, Director of the Central Meteorolog- ical Institute of Sweden, died Oct. 14, aged 73. Joun Hari GLapstox¢, “one of the founders of physical chem- istry,” has died in London at the age of 75. Pmpax FO. VOLUME XILV.* A Academy of Sciences, meeting at Baltimore, 468. Aerodynamics, experiments Langley, 318: André, 398. Alpen, die, im Hiszeitalter, Penck and Briickner, 315. André, M. H., Les Dirigibles, 398. Association, American, meeting at Pittsburg, 166; meeting at Wash- ington, 469. — British, meeting at Belfast, 318. Austin, M., double ammonium phos- phates in analysis, 156. in, B Bacubirito, the great meteorite of Sinaloa, Mexico, Ward, 316. Barbour, E. H., calcite-sand crystal, 451 Barus, C., velocity and structure of the nucleus, 220; ionization of nuclei, 459. Beitrage zur chemischen Physiologie und Pathologie, Hofmeister, 69, 398. Bermuda, ascidians of, Van Name, 74 Black Hills, laccoliths of, Jaggar, 389. Blake, J. C., estimation of bromic acid, 285. BOTANY. Birches, relationships of some Amer- ican and Old World, Fernald, 167. Cyperacez, studies in the, Holm, No. xvi, 97; xvii, 417. Plant growth, relation to ioniza- tion, Plowman, 129. Bottger, W., Grundriss der quali- tativen Analyse, 69. Brewer, W. H., obituary notice of|_ J. W. Powell, 377. British Museum, catalogue of birds’ eggs, Oates, 469. Brown, R. M., clays of Boston Basin, 445, Bumstead, H. A., reflection of elec- tric waves, 309. National, € California, Cretaceous in, 33. — Quaternary history, Hershey, 71. — and Nevada, Triassic Ichthyop- terygia from, Merriam, 467. Cathode rays, effect of ultra-violet light on, Lenard, 67. — laws of velocity of, Gehrcke, 67. Chemie, Lehrbuch der Allgemeinen, Ostwald, 457. Chemische Physiologie und Pathol- ogie, Hofmeister, 69, 398. Chemisches Praktikum, Wolfrum, 385. Chemistry, Elementary, Clarke and Dennis, 305. — First Book of Qualitative, Prescott and Sullivan, 65. CHEMISTRY. Ammonium phosphates in analysis, Austin, 156. Ammonium vanadate, precipitation, Gooch and Gilbert, 205. Arsenic in animal organism, Ber- trand, 3838. Bismuth, radio-active, Marckwald, 503. —1lead sulphide-halides, Ducatte, 64. Bromic acid, estimation of, Gooch and Blake, 285. Carbon, transformation into dia- mond, Ludwig, 4595. compounds, solubilities Speyers, 298. — dioxide, action on the borates of barium, Jones, 49. Chemical combinations, probable source of heat, Richards, 64. Copper sulphate, action upon iron meteorites, Farrington, 33. Glass, plasticity and adhesiveness of, Piccard, 456. of b Helium and liquid hydrogen, Dewar, 305. Hydrogen, liquid, and helium, Dewar, 305. — and oxygen, combination, Baker, 383 ; vapor-pressures of liquid, Travers, Senter and Jaquerod, 311. * This Index contains the general heads, BOTANY, CHEMISTRY (incl. chem. physics), GEOLOGY,, MINERALS, OBITUARY, Rocks, and under each the titles of Articles referring thereto are mentioned. * 472 CHEMISTRY. Iodine pentafiuoride, Moissan, 456. Lithium silicide, Moissan, 64. Manganese, separation from magne- sium, etc., Dietrich and Hassel, 456. Matter, heatless condition of, Brink- worth and Martin, 304. Nitric acid, titrimetric estimation, Phelps, 440. Oxygen and hydrogen, vapor-pres- sures of liquid, Travers, Senter and Jaquerod, 311 ; combination, Baker, 383. Radium, atomic weight, Curie, 384. Rocks in the Nile cataracts, black color of, Lortet and Hagouneng, 64. Silver chabazite and silver analcite, Steiger, 31. Thallium in the thallous Thomas, 385. Thermochemical constant, Clarke, 303. Thiocyanates, Welis, 584. Thiocyauic acid, iodometric titra- tion, Thiel, 455. Uranium, atomic weight, Richards and Merigold, 65. Vanadie acid, reduction of, Gooch and Stookey, 369. Clarke, F. W., Elementary Chem- istry, 305. Coleman, A. P., nepheline and other syenites in Ontario, 147. state, double and triple, Colorado, Silverton quadrangle, economic geology of,. Ransome, 390. Connecticut, Barkhamsted, essonite and corundum at, Emerson, 234. — extent of Newark System, Hobbs, nae — ice sheet in Pomperaug valley, Hobbs, 399. — Tungsten mine at Trumbull, Hobbs, 72. Cornwall, H. B., greenockite on calcite from Joplin, Missouri, 7. Crook, Z. E., electromagnetic alter- nating currents, 133. Cross, W., Chemico-mineralogical Classification of Igneous Rocks, 461. Crystallography, solution of prob- lems in, Renfield, 249. Cumings, E. R., variation in the fossil brachiopod, Platystrophia lynx, 9 INDEX D Davis, W. M., terraces of the West- field River, Mass., 77; Elementary Physical Geography, 318. Dennis, L. W., Elementary Chem- istry, 305. Dewar, J., liquid hydrogen and helium, 805. Dirigibles, Les, André, 398. Dresser, J. A., contribution to the geology of Quebec, 48. Drude, P., Theory of Optics, 68. E Earthquake of 1901 at Inverness, and at Carlisle, Davison, 397. Electric conductibility of metals, Strutt, 459. — discharges through gases, role of self-induction in, Eginitis and de Gramont, 68. displacement, magnetic effect, Whitehead, 109. 4 — resistance of glass, quartz, etc., Rood, 161. — sparks, influence of electrification of the air on, Lecher, 386. waves, interference, tubes for, Becker, 67. — — magnetic detector for, Marconi, 386. — — reflection of, Bumstead, 359. Electricity, removal of negative from the air by rain, Schmauss, 387. Electrolytes, free ions in aqueous solutions of, Olsen, 237. Electromagnetic alternating rents, Crook, 138. Electromotive force of ozone, Brand, 386. Electrostatic tubes, de Nicolaiéve, 386 cur- Emerson, B. K., corundum and a graphitic essonite, 234. Emerson, J. S., characteristics of Kau, 481. Ethnology, Bureau of American, annual report 1901, 470. Evans, N. N., new occurrence of native arsenic, 397. F Farrington, O. C., action of copper sulphate upon iron meteorites. 38. Fernald, M. L., relationships of some American and Old World birches, 167. Fisher, C. A., calcite-sand crystal, 451. INDEX. Ford, W. E., chemical composition of dumortierite, 426. Forest Reserves, U. S., Gannett, 70. G Gesteinskunde fir Techniker, etc., Rinné, 463. Gibbs, J. W., Elementary Principles in Statistical Mechanics, etc., 69. Gilbert, R. D., precipitation of am- monium vanadate, 205. Girty, G. H., upper Permian in west- _ ern Texas, 363. Glass, plasticity and adhesiveness of, Piccard, 456. GEOLOGICAL REPORTS AND SURVEYS. Iowa, 1901, Calvin, 391. Kansas, 461. Louisiana, 314. Michigan, Lane, 393. United States, 21st annual report, 70, 389, 461. GEOLOGY. Alkaline rocks from the region of | Ampasindava, Lacroix, 396. Alpen, die, im Hiszeitalter, Penck and Brickner, 315. Carboniferous ferns, Sellards, 195. Clays of the Boston Basin, Brown, 445. Cretaceous outliers in California, Hershey, 33. — turtles, Wieland, 95. Crossotheca and Myriotheca, fronds of, Sellards, 195. Dikes in Syracuse, New York, erup- tive, Schneider, 24; petrography of, Smyth, 26. Economic geology, Silverton quad- rangle, Col., Ransome, 390. Eocene Mammalia in the Marsh col- lection, studies of, Wortman, 17. Eparchean interval, Lawson, 71. Eruption of Mt. Pelee, 312, 319; peculiar character of, Verrill, 72. Eskers, origin of, Crosby, 316. Fossil brachiopod, Platystrophia lynx, variation in, Cumings and Mauck, 9. — plant from Illinois, Sellards, 203. — vertebrata of North America, bib- liography and catalogue, Hay, 390. | 473 Geologic formation namesof North America, Weeks, 391. Geology of Quebec, contribution to, Dresser, 43. Ice-sheet, action of, on projecting rock masses, Hobbs, 399. Idiophyllum rotundifolium, valid- ity of, Sellards, 203. Igneous rocks, chemico-mineralog- ical classification, Cross, Iddings, Pirsson and Washington, 461. — — size of grain in, Queneau, 70; Lane on Queneau, 393. Laccoliths of the Black Hills, Jag- gar, 389. Lowlands of southeastern Missouri, evolution of, Marbut, 392. Mammalia, Eocene in Marsh col- lection, 17. Monzoni region in the Tyrol, petrog- raphy and geology, Romberg and Doelter, 463. Newark system, former extent of, Hobbs, 71. Niagara limestones of Indiana, Kin- dle, 221. Permian, upper, in western Texas, Girty, 363. Platystrophia lynx, variation in the fossil brachiopod, Cumings and Mauck, 9. Pleistocene geology of western New York, Fairchild, 393. Plissements et dislocations de Vécorce terrestre en Grece, Negris, 71. Potomac group of the middle At- lantic slope, geology, Clark and Bibbins, 392. Quaternary history of California, Hershey, 71. Rocks in the Nile cataracts, black color of, 64. Terraces of the Westfield River, Mass., Davis, 77. Triassic _Ichthyopterygia from Cal- ifornia and Nevada, Merriam, 467. Vertebrates of the Northwest Ter- ritory, Osborn and Lambe, 393. Voleanic eruptions of 1902 on St. Vincent and Martinique, 72, 312; Hovey, 319. Volcanoes, Hawaiian, Kau, Emer- son, 431. Gooch, F. A., precipitation of am- monium vanadate, 205; estimation of bromic acid, 2850; reduction of vanadic acid, 369. Grundriss der qualitativen Analyse, Bottger, 65. southern 474 H Havana, study of yellow fever in, Gargas, 79. Hawaii, the volcano of Kau, Emer- son, 481. Hershey, O. H., Cretaceous outliers in California, 33. Hillebrand, W. F., additions to the Alunite-Jarosite group, 211. Hobbs, W. H., action of ice-sheet on projecting rock masses, 399. Hodgkins gold medal awarded, 470. Hofmeister, F., Beitrige zur chem- __ischen Physiologie, 69, 398. Holm, T., studies in the Cyperacee, No. xvi, 57; xvii, 417. Holtz machine, new, Wommelsdorf, 4959. Hovey, E. O., eruptions of 1902 on St. Vincent and Martinique, 319. Hydrogen, spectra of, Trowbridge, 457. I Iddings, J. P., Chemico-mineralogi- cal Classification of Igneous Rocks, 461. Indiana, Niagara limestones of, Kin- dle, 231. International Quarterly, 318. Iowa geological survey, 1901, 391. J Jones, L. C., action of carbon diox- ide on the borates of barium, 49. K Kansas geological survey, 461. Kau, characteristics of, Emerson, 481. Kayser, Hk, Handbuch der Spectro- scopie, 460. Kindle, E. M., Niagara limestones of Indiana, 221. Koenig, S A., new species melano- chalcite and keweenawite, 404. Lc Lacroix, A., \iinéralogie de la France et ses Colonies, 70. Lane, A. C., Queneau on size of grain in igneous rocks, 393. Langley, S. P., Experiments in Aero- dynamics, 318. La Soufriére, St. Vincent, and Mt. Pelée, Martinique, eruptions of, Hovey, 319. Light, electrical effect of, Lenard, 67. .Louisiana geological survey, 314. INDEX. M Maldive and Laccadive Archipela- goes, Gardner, 74. Marsh collection, studies of the Eocene mammalia, Wortman, 17. Martinique, 72, 312. — and St. Vincent, eruptions of 1902, Hovey, 319. Massachusetts, Boston Basin, clays of, Brown, 445. — Westfield River, terraces of, Wis Mauck, A. V., variation in the fossil brachiopod, Platystrophia lynx, 9. Measurement of 98th meridian, 469. Mechanics, Elementary Principles in Statistical, Gibbs, 69. Metals, electrical conductibility of, Strutt, 459. — reflection power for ultra-violet and ultra-red rays, Hagen and Rubens, 66. ee Meteorite, iron, from Sinaloa, Mex- ico, Ward, 316 Meteorites, action of copper sulphate upon, Farrington, 38; gold in, Liversidge, 466. Mexico, Sinaloa, meteorites from, 316. a geological survey, Lane, 93. Mineral resources of So. O’Harra and Todd, 897. . . — — of the United States, 1901, Day, 461. — waters, Bailey, 461. Dakota, 'Minéralogie de la France et de ses Colonies, Lacroix, 70. MINERALS. Alunite, Colorado, 216. Analcite, dl. Arsenic, native, 807. Baumhauerite, "464, Calcite-sand crystal, new form, 451. Chabazite, 31. Coloradoite, 465. Coolgardite, 465. Corundum, 234. Dumortierite, chemical composition, 426. Essonite, graphitic, 234. Garnet, 234. Gold in meteorites, 466. Greencckite on calcite, Joplin, Missouri, 7. Histrixite, 466. Hussakite, 316. Jarosite, 216. Keweenawite, Michigan, 410. Kill- rickerite, 464. Marshite, 465. Melanochalcite, Arizona, 404. _Melilite, Syracuse, INFN Gr Mercury-deposits in Texas, "464. Miersite, 465. Natrojarosite, Nevada, 211. INDEX. MINERALS. Petterdite, 466. New Mexico, 213. Stibiotantalite, 466. Xenovtime, 316. Missouri, evolution of the lowlands of southeastern, Marbut, 392. Mt. Pelée, 312, 319; peculiar char- acter of the eruption of May 8th, Verrill, 72. Plumbojarosite, N New York, Syracuse, eruptive dikes in, Schneider, 24; petrography of dikes, Smyth, 26. — Western, pleistocene geology of, Fairchild, 393. Nile cataracts, black color of rocks in, Lortet and Hugouneng, 64. Noyes, A. A., General Principles of Physical Science, 457. Nucleus, velocity and_ structure, Barus, 225; ionization of, Barus, 459. O OBITUARY. Gladstone, J. H., 470. Kedzie, R. C., 470. Powell, J. W., 377. Riva, Dr. Carlo, 166. Rood, O. N., 470. Rubenson, R., 470. Virchow, Rudolph, 318. Olsen, J., free ions in aqueous solu- tions of electrolytes, 237. Ontario, syenites in,Coleman, 147. Optics, theory of, Drude, 68. Ostwald, W., Lehrbuch der Allge- meinen Chemie, 457. Ostwald’s Klassiker der Exakten Wissenschaften, 76, 470. pe” electromotive force of, Brand, 86. P Penfield, S. L., solution of problems in crystallography, 249. Phelps, I. K., titrimetric estimation of nitric acid, 440. Phonetics, Elements of Experimen- tal, Scripture, 387. Physical Geography, Gilbert and ao 398 ; Klementary, Davis, 8. — Science, General Principles of, Noyes, 457. Pirsson, L. V., Chemico-mineralogi- ce Classification of Igneous Rocks, 61, 475 Plowman, A. B., relation of plant growth to ionization, 129. Porto Rico, actinians of, Duerden, 74, Powell, John Wesley, obituary no- tice, Brewer, 377. Prescott, Qualitative Chemistry, 65. Q Quebec, petrographical contribution to the geology. of, Dresser, 43. Queneau on size of grain in igneous rocks, 70; Lane, 398. R Radio-active bismuth, Marckwald, 303. — substances, Rutherford and Grier, 387; radiations, Rutherford and Brooks, 326. Radioactivity in air, Thompson, 387. Rinné, F., Gesteinskunde fiir Tech- nicker, etc., 463. ROCKS: Dahamite, Pelikan, 397. Eleolite syenite, Morozewicz, 396. Mariupolite, Morozewiez, 396. Nepheline syenites, Ontario, 147. Syenites, Ontario, 147. Rood, O. N., electrical resistance of glass, quartz, etc., 161. Ss St. Vincent and Martinique, erup- tions of 1902, 72, 312 ; Hovey, 319. Scientia, 76. Scientific Literature, Catalogue, 317. Schneider, P. F., eruptive dikes in Syracuse, New York, 24. Scripture, E. W., Elements of Ex- perimental Phonetics, 387. Self-induction, role of in discharges of electricity through gases, Hgin- itis and de Gramont, 68. Sellards, E. H., fronds of Crosso- theca and Myriotheca, 195 ; validity of Idiophyllum rotundifolium, 203. Smithsonian Institution, annual re- port, 1901, 469; publications of, 76. Smyth, C. H. Jr., petrography of dikes in Syracuse, N. Y., 26. South Dakota, mineral resources, O’Harra and Todd, 397. Spark discharge from metallic poles in water, Wilsing, 67. International 4776 Spectra from the dissociation of water vapor, Trowbridge, 1. ee hydrogen and gases, Trowbridge, Spectroscopie, Handbuch der, Kay- ser, 460. Spectrum of Novae, cause of pecu- liarities in, Wilsing, 67. Speyers, C. L., solubilities of some carbon compounds, 293. Steiger, G., silver chabazite and silver analcite, 31. Stookey, L. B., reduction of vanadic acid, 369. Sullivan, Qualitative Chemistry, 65. SO Terlingua quicksilver deposits, Texas, 464. Texas, northwest boundary of, Baker, 391. — upper Permian in western, Girty, 369. — Terlinqua quicksilver deposits, 464. Thermo element, vacuum, Lebedew, 389. Trowbridge, J., spectra from the dissociation of water vapor, 1; spectra of hydrogen and reversed lines in the spectra of gases, 457. Tungsten mine, at Trumbull, Conn., Hobbs, 72. Turtles, Cretaceous, Wieland, 95. Tyrol, petrography and geology of the Monzoni region, Romberg and Doelter, 463. U Ultra-red rays, reflection power of metals for, Hagen and Rubens, 66. Ultra-violet rays, reflection power of metals for, Hagen and Rubens, 66. United States Coast Survey, annual report, 1901, 469. — — Geol. Survey,21st annual report, 70, 389, 461, Bulletins, 390, 391, 461 ; mineral resources, 461. INDEX. United States National Museum, list of publications, 469. — — Naval Observatory, 470. — — Weather Bureau, 76. V Verrill, A. E., peculiar character of the eruption of Mt. Pelee, 72. Volcanic eruptions on St. Vincent and Martinique, 72, 312, 319. W Washington, H. S., Chemico-min- eralogical Classification of Igneous Rocks, 461. Whitehead, J. B., Jr., magnetic effect of electric displacement, 109. Ween G. R., Cretaceous turtles, Wolfrum, A., Chemisches Prakti- kum, 385 Wortman, J. L., Eocene Mammalia. in the Marsh collection, studies of, 17. Zz Zoological Results from New Britain,. New Guinea, etc., Willey, 468. ZOOLOGY. Actinians of Porto Rico, Duerden,,. Ascidians of ‘Bermuda, Van Name, Brachiopod, embryology of, Conk-. tim, Vo: Corals of Maldive and Laceadive Archipelagoes, Gardner, 74. Nautilus from New Britain, etc., Willey, 468. Stegomyia fasciata infected by yel- low fever in Havana, study of,. Gargas, 75. oi stv. gl JULY, 1902. Established by BENJAMIN SILLIMAN in 1818, oY See i a we s AMERICAN }JOURNAL OF SCIENCE. Epitor: EDWARD S. DANA. ASSOCIATE EDITORS | Prorzssors GEO. L. GOODALE, JOHN TROWBRIDGE, [J | W.G. FARLOW anp WM. M. DAVIS, or CamsripcE, a «, - e ok : ; ~ ‘ ; | 7 a q < ~ 4 2 ee ede my (tae ee hs Op eh ie aie} © r) Ea) ere 2 is aa e's teed. pee ee i pe te aad eau A¢ Ste ae oe gale ise i eee AEN rete a per or) ChE }| Proressors A. E. VERRILL, HENRY S. WILLIAMS anp a | L. V. PIRSSON, or New Haven. Proressor GEORGE F. BARKER, or PHILADELPHIA, , _ ProFressor JOSEPH S. AMES, or Battimorg, a Mr. J. S. DILLER, or WasHINGTON. ay FOURTH SERIES. ee VOL. XIV—[WHOLE NUMBER, CLXIYV.] ae x : No. 79.—JULY, 1902. | WITH PLATES I-III. é dk 5 naa J : LE din § ~ “4,8 t/t! = f wt loti Pi. tae i e oes He F e-8y ate Aa Slik vs er rae ‘toa a9 i % ar. re eke Aa, oe een SIRT ee Wied : NEW HAVEN, CONNECTICUT. ee eee 1902. m= A. oar ce 0b RES wa Ate ee : Ny Bs _ THE TUTTLE, MOREHOUSE & TAYLOR CO., PRINTERS, 125 TEMPLE STREET, ‘ublished monthly. Six dollars per year, in advance. - $6.40 Union. Remittances should be made either by money : Has bank checks Ceseeer by on New York banks). Zs OPES! i the, /) ders, registered % JUL 3) 1902/ SAPPHIRE BLUE of the true shade is to be found in the popularly named “ False Sapphire” or CYANITE from the far-famed St. Gothard. A trip by our collector and considerable work done for us yielded some superb specimens. This locality has been known for over half a century, but like many others in Switzerland, is quite unworkable, save during two months of the year, and rarely visited even then. Thus the specimens are not new—just vastly supe- rior to those in the large museums, all of which have the early specimens, but are fast replacing them with the later ones, Months of expert work were devoted to the careful removal of the Para- gonite matrix, exposing the transparent blue crystals associated with lustrous dark brown Staurolites, often in parallel and penetrating habits. This is mentioned in some of the mineralogies, which likewise add ‘‘ rarely termi- nated.” Yet we have perfectly terminated Cyanites six inches long, pene- trating the length of a Staurolite. This peculiarity, together with the contrasting blues and browns standing out on the pearly background, affords one of the most striking combinations to be seen in any collection. The stock of really fine specimens is limited and rapidly diminishing. 50e. to $15.00. Detached Crystals, 25c. per dozen to $1.00 each. Terminated Crystals, 50c, to $2.00 each, OTHER SWISS MINERALS. We secured by exchange the few duplicates left in one of the oldest of European collections. Among them were the following historical things of high value: Hisenrose, Sphene, Octahedral Rose Fluor, Axinite, Apatite, Green Fluor, Smoky Quartz, ete., ete. EDUCATIONAL COLLECTIONS. For 26 years we have supplied mining schools, universities, colleges and secondary schools throughout the world with mineralogical material, Dur- ing that period the quality of our elementary and advanced collections has steadily improved, so that to-day the highest grade of study specimens are offered at unprecedentedly low prices. An inspection of our Laboratory List will show that European minerals are sold not simply below American prices, but often at lower rates than prevail in Europe. The wide connec- tions of our European house alone permit this economy to the consumer, our prices being the same on both sides of the Atlantic. If in Paris this summer favor us with a call—15 minutes from the Opera Quarter. Illustrated Collection Catalog Free, The Largest and Most Complete Stock of Scientific and Educational Minerals in the World, Highest Awards at Nine Expositions. FOOTE dCi 250.4200 Gee FORMERLY DR. A. B, FOOTE, PHILADELPHIA, PARIS, 1817 Arch Street, 24 Rue du Champ de Mars. Dr. Cyrus Adler, | 2 RR aot ce aie aes si: Librarian U. S, Nat. Mase. ad ok sees A A 7 Sea ie ae dee re deechs Be AGB, 1908. i a Established by BENJAMIN SILLIMAN in 1818. AMERICAN 3 JOURNAL OF SCIENCE. Epitorn: EDWARD S. DANA. [s : ASSOCIATE EDITORS | Proressors GEO. L. GOODALE, JOHN TROWBRIDGE, ae _ W. G, FARLOW anp WM. M. DAVIS, or Camprince, a _ Proressors A. E. VERRILL, HENRY S. WILLIAMS anv |[ Ll: V-- PERSSON; oF NEw HAVEN, — aa. PROFESSOR GEORGE. F. BARKER, OF PHILADELPHIA, = Proressor JOSEPH S. AMES, oF BALTIMORE, na = Mr. J. S. DILLER, or Wasuincrton. : FOURTH SERIES. : i ‘VOL. XIV-[WHOLE NUMBER, CLXIV] - i No. 80.—AUGUST, 1902. ee i: WITH PLATE IV. bere NEW HAVEN, CONNECTICUT. | a its A 5 Se t AGS 2 ey en : ye hd. = THE TUTTLE, MOREHOUSE & TAYLOR CO., PRINTERS, 125 TEMPLE STREET. is ss lished monthly. Six dollars per year, in advance. $6.40 to countries in the | Union. Remittances should be made either by money orders, registered or bank checks spent on New York banks). ! SAPPHIRE BLI of the true shade is to be found in the popularly named “‘ False S phi or CYANITE from the far-famed St. Gothard. Foote Miwa A cee FORMERLY DR. A. E. FOOTE, PHILADELPHIA, PARIS, 1317 Arch Street. ; 24 Rue du Champ de Mars. : ~ Sys ? “” ey Fes 7 te NEO fit ai ee a in = Cur’ < ri 4; ia Mes by BENJAMIN a: ae THE. ae ee 2 " AMERICAN Eprror: EDWARD S. DANA. - ASSOCIATE EDITORS rEssORS Been VERRILL, HENRY ‘SS. WILLIAMS anp PV. PIRSSON, oF New Haven, ~ PRovEssor JOSEPH oF AMES, OF BALTIMORE, Mr. J. S. DILLER, or Wasurncron. oe FOURTH SERIES. _ Vor. XIV—[WHOLE NUMBER, CLXIV.] No. 81.—SEPTEMBER, 1902. WITH PLATES Y-VII. - NEW HAVEN, CONNECTICUT. EO. > Shi H ; TUTTLE, MOREHOUSE & TAYLOR CO., PRINTERS, 125 TEMPLE STREET.- Se URhie Six dollars per year, in advance. $6.40 to countries in the .. Remittances should be_made either by money orders, registered — “ES sureteceby on 1 N ew York Hse) URNAL OF SCIENCE. SS aS ear re ’ a a eee ok eee ae ee, a ae oe ,. nee ed Ae ee : Cs A ised Pe ie eee , i 4 , ‘ . r “ ‘ ) é +3 characteristic habits. Breislakite, Hauynite. Ten months were spent eae our collector in visiting the es tions and several of the most important localities. A large numb specimens were thus secured, which cannot be duplicated eve: tempting exchanges that can be personally offered. But few good miner a now coming from the mines of the peninsula, and the high values plac examples of the old tinds are steadily rising. The following are all good examples of their kind, extra choice crystallizations being Coie we : - PIEDMONT - Piedmontite, V iolan, Diopside, Idocrase, large Hessonite Bi of fine quality. BAVENO (At lower prices than foreign collectors pay at the quarries.) a Bayenite, a very rare new species, Babingtonite, rare, Orthoclase in Ba and Manebach twins, Fluorite. CARRERA Limpid Rock Crystal on Marble. : PORRETTA A large assortment of the well known cavernous Quartz Crystals, many sho moving bubbles, Calcite in neat groups of primitive rhombs. — ELBA : A large lot of Tourmaline crystals including excellent terminations, green and white. A few vari-colored. Cookeite, Ilvaite, Pollucite. We maintain: the old scale of prices on this consignment in spite of a great advance in Tal BELLISIO SOLFARE ey Sulphur in brilliant transparent crystals of different types from the Site and of finer quality. Selenite, perfectly limpid and flawless crystals of unrivalled lustre, offering the most highly prized specimens of this mineral known. ee 3 with the Sulphur and isolated. A remarkably beautiful but rare occnrrenee- : CAPO DI BOVE ae Nephelite in groups of sharply defined hexagons. Gismondite ayeie 0! MONTE SOMMA : “What's in a name” is answered for the mineralogist in the eee is. Of some of them we obtained but one specimen, and at ‘the best got but a sad from which Prof. Scacchi made the descriptions: _ Granuline Neochrysolite Melanothallite I Neociano Nocerite Sodalite, well eer : Euchlorite Aphthitalite, fine crystals Thermonatrite ce Humboldtilite Belonesite with Humite Cuspidine Cryphiolite Hydrodolomite Meionite, large xls Séméline Hydrccyanite Erythrocalcite Facellite, fine group of : Dolerophanite crystals | a Illustrated Collection Catalog Free. The Largest and Most Complete Stock of Scientific and Educational Mine in the World. gas pare Awards at Nine Expositions. FORMERLY DR. A. E. FOOTE, PHILADELPHIA, ee - PARIS{S 22 1317 Arch Street. 24 Rue du Champ de Mar . ‘Cyrus Adler, Librarian U. S. Nat. Museum. OCTOBER, 1902. Established by BENJAMIN SILLIMAN in 1818. THE AMERICAN Epitor: EDWARD S. DANA. are ASSOCIATE EDITORS - EV. PIRSSON, or New Haven, PROFESSOR GEORGE F. BARKER, or PHILADELPHIA, ProFEssor JOSEPH S. AMES, or BALtTImore, Mr. J. S. DILLER, or WASHINGTON. FOURTH SERIES. VOL. XIV—[WHOLE NUMBER, CLXIV.] No. 82.—OCTOBER, 1902. NEW HAVEN, CONNECTICUT. / ZS. , OF, " THE TUTTLE, MOREHOUSE & TAYLOR CO.,, ay S, 125 TEMPLE STREET. Pee hlished monthly. Six ALTIUS Asace $6.40 to countries in the Postal Union. Remittances should ffiade either by money eects registered tter or bank checks (preferably on New York banks). (oes eee _— re * Fg as ons, oe a any i my Lael ey a ITALIAN MINERAI MANY IMPORTANT RARITIES. bac Ten months were spent by our collector in visiting the principal mineral coll tions and several of the most important localities. A large number of histori specimens were thus secured, which cannot be duplicated even by the m tempting exchanges that can be personally offered. But few good minerals ar now coming from the mines of the peninsula, and the high values placed upon examples of the old finds are steadily rising. The following are all good typica examples of their kind, extra choice crystallizations being osucerne noted. ms PIEDMONT Piedmontite, Violan, Diopside, Idocrase, large Hessonite crystals of unusually 2 fine quality. lc hae BAVENO ’ (At lower prices than foreign collectors pay at the quarries.) Bavenite, a very rare new species, Babingtonite, rare, Orthoclase in Baveno and Manebach twins, Fluorite. 3 CARRERA cea Rock Crystal on Marble. PORRETTA . et A large assortment of the well known cavernous Quartz Crystals, many showing ets bubbles, Calcite in neat groups of primitive rhombs. ELBA . eee A large lot of Tourmaline crystals including excellent terminations. Red, ~ green and white. A few vari-colored. Cookeite, Ilvaite, Pollucite. Wemaintain ~~ the old scale of prices on this consignment in spite of a great advance in Italy. BELLISIO SOLFARE . fon Sulphur in brilliant transparent crystals of different types from the Sicilian and of finer quality. Selenite, perfectly limpid and flawless crystals of unrivalled lustre, offering the most highly prized specimens of this mineral known. Grouped with the Sulphur and isolated. A remarkably beautiful but rare occurrence. — CAPO DI BOVE < : Po Nephelite in groups of sharply defined hexagons. Gismondite crystals of characteristic habits. Breislakite, Hauynite. . ; ¥ MONTE SOMMA ‘What's in a name” is answered for the mineralogist in the following list. Of some of them we obtained but one specimen, and at the best got but a sadly limited supply. All are old and quite’a number are of the original meagre fee so oe from which Prof. Scacchi made the descriptions :— : Granuline ; Neochrysolite Melanothallite Neociano Nocerite Sodalite, well crystallized — Euchlorite Aphthitalite, fine crystals Thermonatrite Humboldtilite Belonesite with Humite Cuspidine Cryphiolite | Hydrodolomite Meionite, large xls Séméline Hydrceyanite Erythrocalcite Facellite, fine group of Dolerophanite crystals Illustrated Collection Catalog Free. The Largest and Most Complete Stock of Scientific and Educational Minerals in the World. reas tae Vg Awards at Nine Expositions. a ES NENT eA Coes FORMERLY DR. A. E. FOOTE, PHILADELPHIA, PARIS, 1317 Arch Street. : 24 Rue du Champ de Mars. # y T U Ss Aaler, 4 ian U. S. Nat. Museum. s AMERICAN URNAL OF SCIENCE. _ Eprror: EDWARD S. DANA. ASSOCIATE EDITORS oe GEO. L. GOODALE, JOHN TROWBRIDGE, L. V. PIRSSON, oF NEw fies - Proressor GEORGE F. BARKER, oF PHILADELPHIA, _ PROFESSOR JOSEPH S. AMES, or Battimorg, Mr. J. S. DILLER, or WasutncTon. FOURTH SERIES. No. 83.—NOVEMBER, 1902. WITH PLATE VIII. NEW HAVEN, CONNECTICUT. 0/9 1909. . Shona Huse’ “ete ~*~ blished monthly. Six dollars per year, in advance. $6.40 to countries in the Union. Remittances should be made either by money orders, registered co Pails checks Se on New York erste WYER LO “ Several recent’ shipments aoe from ae oe of A cabinet specimens. Small study specimens SS 15c. 6 40e. z Hematite in hexagonal = New: and rare. ae examples, but of different erystalline habit. Rose Apophyllite in handsome groups. Beautifat white and co. pS a erystallizations. Also detached crystals. pase aS Hyalite. Clear masses of pearly lustre in twisted and botryoi & Attractive and typical. | ae Bais: : Fire Opal in large pieces. ogre i= sie : Octahedral Fluor showing interesting modifications. — = ee | Quartz Crystals containing moving bubbles. Saas Amethyst in groups of unrivaled richness and depth of oglege “be Stilbite. Delicate cream-colored groups. Crystals symmetrical sind wells ) | defined. ea offered at sinpiecod sakeaie oh low prices. An inspection of our Laborato tag List of minerals for analysis, will show that European minerals are sold me simply below American prices, but often at lower rates than prevail — Europe. The wide connections of our European house alone permit 1] economy to the consumer, our prices being the same on both sides ery | Atlantic. > Illustrated Collection abi Free. Foote MINERAL co. FORMERLY DR. A. E. FOOTE, PHILADELPHIA, oan F 1317 Arch Street. 24 Rue du Champ de Mars. _ Cyrus Adler, Librarian U. S. Aa THE AMHRICAN Epror : EDWARD S. DANA. 7 Sr | ASSOCIATE EDITORS BSSORS GEO. L. GOODALE, JOHN TROWBRIDGE, FOURTH SERIES. VoL, XIV—[WHOLE NUMBER, CLXIV.]. No. 84.—DECEMBER, 1902. ee WITH PLATE IX. re NEW HAVEN, CONNECTICUT. /7% 3: 1902. hed monthly. Six dollars per year, in advance. $6.40 to mere in the mn. Remittances should be made either by money orders, registered es checks. Se a on New RES banks). ———————— oe = steadily improved, so that to-day the highest grade of study specimens are ~ Several recent shipments direct from the ‘‘ Andreasberg of America”? +8 afford a large choice of the more recent-finds of this famous district. Prices -average lower than formerly, generally 50c. to $3.00 or $4.00 for the best sy cabinet specimens. Small study specimens at 15c. to 40e. Hematite in hexagonal prisms. New and rare. Small but marvel- ously sharp and brilliant, coating a volcanic rock suggesting the Vesuvian examples, but of different crystalline habit. Rose Apophyllite in handsome groups. Beautiful white and colorless erystallizations. Also detached crystals, Hyalite. Clear masses of pearly lustre in twisted and botryoidal forms. | Attractive and typical. Fire Opal in large pieces. Fe Octahedral Fluor showing interesting modifications. Quartz Crystals containing moving bubbles. - : Amethyst in groups of unrivaled richness and depth of color; 45558 , Re za Stilbite. Delicate cream-colored groups. Crystals symmetrical and well . defined. f st STUDY SPECIMENS — For 26 years we have supplied mining schools, universities, colleges aie secondary schools throughout the world with mineralogical material. . “Dur- ing that period the quality of our elementary and. adyanced- collections: has — offered at unprecedentedly low prices. An imspection of our Laboratory ie List of minerals for analysis will show that European minerals are sold not ~ simply below American prices, but often at lower rates than prevail in 3 Europe. The wide connections of our European house alone permit this economy to the consumer, our Pass being the same on both sides of the Atlantic. Illustrated Collection Catalog Free. The Largest and Most Complete Stock of Scientific and Educational Minerals. t in the World. Highest Awards at Nine Expositions. Foote MINERAL CO... a FORMERLY DR. A. E. FOOTE, PHILADELPHIA, PARIS, 1317 Arch Street. 24 Rue du Champ de Mars. et 313 a (H ) NIA ii 3 90 ARIE WAMU 88 01298 5651 80