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** Ferrogenic Function.

A. The following drugs caused a very marked diminution in the amount of free iron in the liver :

Sodium iodide, toluene, toluylene diamine.

B.-The following caused a diminution in the quantity of iron, but not to the same extent as the first, and the iron was often so distributed as to remind one of the appearances observed in an active liver:

Chloride of ammonium, nitric acid, pilocarpine, benzol (in the fed liver).

C.-In one case only a doubtful increase of iron was found :-
Benzol (in the fasting liver).

2. In the group of depresso-secretory compounds.

A.-Ammonia caused a diminution of the glycogen and an increase

of iron.

By its influences on the accumulation of glycogen and of iron, phenol acts distinctly in the same way as the depresso-secretory compounds; thus it caused diminution in the glycogen and an increase in the iron.

Aniline caused little change in the glycogen, but a great accumulation of iron in one case. The action of aniline evidently requires to be studied more specially.

B.-Atropine caused a slight diminution in the glycogen and little change in the iron.

General Concluding Remarks.

We are satisfied that much is to be learned of the affinities of drugs and of their physiological action by the methods which we have been using in this study. The anticipation of unknown difficulties in a field. practically new has caused us to spend much time in observations which have not all proved of much use. We know now how to obtain those results which are most useful. We are repeating some of the experiments in order to test the value of our first results, and we are slowly repeating the measurements which have already taken such a considerable amount of time. It would be unwise in the present state of the inquiry to attempt to give more dogmatic conclusions than those we offer provisionally.

VIII. "Note on the Production of Sounds by the Air-bladder of certain Siluroid Fishes." By Professors T. W. BRIDGE and A. C. HADDON. Communicated by Professor A. NEWTON, F.R.S. Received April 17, 1894.

66

Dr. William Sörensen, of Copenhagen, has drawn our attention to the fact that, in our memoir on The Air-bladder and Weberian Ossicles in the Siluroid Fishes," published in the Philosophical Transactions' last year (vol. 184, pp. 65-333), we failed to do justice to the results of certain investigations which are embodied in his paper, entitled "Om Lydorganer hos Fiske: en physiologisk og comparativ-anatomisk Undersögelse," and published at Copenhagen in 1884. In this paper Dr. Sörensen treats of the various methods of sound production in Fishes in general, and in the case of the Siluroid Fishes, describes the production of sounds by means of certain stridulating mechanisms (friction of the dorsal and pectoral spines), the "elastic spring" apparatus, and the paired extrinsic muscles of the air-bladder in the Pimelodina. We do not here wish to criticise his morphological conclusions, but to point out that, contrary to the assumption on pp. 270 and 301 of our paper, Dr. Sörensen did make some experiments on living Fish. After describing the nature of the "elastic spring" and the disposition of its muscles in the South American Siluroid, Doras maculatus, on p. 88 of his paper, he says, concerning this Fish :

:

"Observations on the Production of Sounds.-When one opens the abdomen of a recently caught fish and quickly extracts the intestines with everything that is attached to them so that the swim-bladder is exposed, one can very easily perceive that the swim-bladder is in a convulsive vibratory motion at the same time that the sound is produced. It is a very deep murmuring note, which is so strong that it can be distinctly heard at a distance of 100 ft. when the animal is out of the water. Unlike the sounds produced by the movements of the pectoral fin, the tones produced by the swim-bladder are not grating, and therefore not disagreeable to the ear. As far as I am able to judge, the swim-bladder commands only one note, but this can be stronger or weaker according to the will of the fish. If one moves the fingers backwards and forwards over the swim-bladder, one will soon perceive that the vibrating motion, beginning at the same time as the sound, is strongest in the front, especially at the "muscle-springs," and also that the muscles passing to these contract at the same time that the sound is produced. If the muscles are cut through, the sound is no longer produced. If one makes a little hole in the swim-bladder, the sound will not be very much weaker; but if

a larger opening is made in it, the sound will considerably diminish in strength. If one takes out the swim-bladder, the note will become very weak, but may still be heard; it is then produced only by the vibrations of the springs. By ordinary observations I have not been able to prove that those bars or cross-walls (transverse septa) which project into the lumen of the chief compartment of the swim-bladder, or its external diverticula, assist in the production of sound; but if one compares this with what I state later on in Pseudaroides, I believe it would prove very doubtful, on account of their incomplete partition walls, that the diverticula of the swim-bladder even to a great degree serve to strengthen the sound by the air passing to and fro over them. By looking more particularly one will observe that the anterior cutaneous plate at the side of the body also vibrates when the sound is produced. I suppose that the action of the ligament, which connects it with the circular plate of the muscular spring, besides transferring the sound vibrations of the swim-bladder to the water, consists in preventing a too violent recoil of the spring when the muscle is relaxed."

After describing the air bladder, and the arrangement of its paired extrinsic muscles in Platystoma orbignyanum, and Pseudaroides clarias, Dr. Sörensen continues (p. 93):-" When the swimbladder is laid open in the living animal, it is very easy to perceive that the contractions of the previously mentioned muscles [extrinsic muscles] occur at the same time as the production of a strong, deep, murmuring sound, whilst the wall of the swim-bladder is put into strong vibratory motion. The majority of the specimens I have examined of Pseudaroides had at the most a total length of 25-35 cm. The walls of the swim-bladder were, therefore, not so thick, but I was able to distinguish the internal transverse septa as darker transverse lines; I could therefore see very distinctly that when the sounds were produced, the septa were in a state of rapid vibration forwards and backwards. This is sufficient to prove that they play a very important part in tending to increase the sounds by the fact that the air vibrates over their free edges, from one chamber to the other. If one makes a small hole in the swim-bladder of Platystoma, the strength of the sounds will not be very much diminished. If an even smaller incision is made the sound becomes fainter and fainter, and at length dies away, even though the muscles are functional."

"So far as I have been able to see, only one muscular contraction takes place, as in Doras, for every time sound is produced. This always lasts a certain period, is fainter at the end, but ceases suddenly. About the nature of the sound, the same can be said as I have stated about Doras. The sound a Platystoma produces can be heard at a distance of more than 20 feet, when the animal is on the land."

From these observations it is also clear that the sounds produced by these fishes are not caused by the expulsion of air through the ductus pneumaticus, as erroneously assumed by us on pp. 298 and p. 301 of our memoir, but are caused by the vibration of the air within the air-bladder, which is set in motion either by the "elastic spring" apparatus, or by the extrinsic muscles.

The investigations of Dr. Sörensen seem to show that, under certain conditions, the "elastic spring" mechanism, and the paired extrinsic muscles of the Pimelodine, are structures subordinate to sound production, and are not, as we suggested, related to any method of adjustment to varying hydrostatic pressures. Had we appreciated this fact earlier, we should have modified certain of the tentative conclusions suggested on pp. 298-301 of our memoir. On the present occasion we wish to draw the attention of those interested in the subject to Dr. Sörensen's researches, and at the same time to express our regret at the injustice we have unintentionally done. him.

The Society adjourned over Ascension Day to Thursday, May 10.

Transactions.

Presents, April 26, 1894.

Buitenzorg:-Jardin Botanique. Annales. Vol. XII. Partie 1.
8vo. Leide 1894.
The Director.
Edinburgh :-Botanical Society. Transactions and Proceedings.
Vol. XIX. Pages 233-636. 8vo. Edinburgh 1893.

The Society.
Haarlem .—Musée Teyler. Archives. Vol. IV. Partie 2. Svo.
Haarlem 1894.
The Museum.
Irkutsk :-East Siberian Section, Imperial Russian Geographical
Society. Annual Report. 1892. [Russian.] 8vo. Irkutsk
1894.
The Society.
Kazan:-Imperial University. Scientific Notes. [Russian.] 1894.
No. 4. 8vo. Kazan.
The University.
Kew-Royal Gardens. Bulletin of Miscellaneous Information.
1894. No. 88. 8vo. London.
London:-Aristotelian Society for the Systematic Study of Philo-
sophy. Proceedings. Vol. II. No. 3. Part I. 8vo. London
1894.
The Society.

The Director.

City and Guilds of London Institute. Report to the Governors, 1894. 8vo. London. The Institute. Marine Biological Association. Journal. Vol. III. No. 2. 8vo. London 1894. The Association. Marseilles-Faculté des Sciences. Annales. Tome III. Fasc. 4. 4to. [Marseille 1893.]

The Faculty.

Transactions (continued).

Paris-Ecole des Hautes Études. Bibliothèque. Fasc. 97, 99.

8vo. Paris 1893-94.

The School.
Société Géologique. Bulletin. Vol. XXI. No. 4. 8vo. Paris
1893.
The Society.

Pisa-Società Toscana di Scienze Naturali. Atti.

Vol. XIII.

8vo. Pisa 1894; Processi Verbali. Vol. IX. Pages 1—62 8vo. Pisa 1894. The Society. Prague-Gesellschaft zur Förderung Deutscher Wissenschaft, Kunst und Literatur in Böhmen. Mittheilung. Nr. 1. 8vc. Prag 1894. The Society. St. Petersburg:-Kais. Akademie der Wissenschaften. Repertorium für Meteorologie. Bd. XVI. 4to. St. Petersburg 1893.

Siena :-R. Accademia dei Fisiocritici.

The Academy.

Atti.

Vol. II.

Fasc. 5—6.

8vo. Siena The Academy.

Vol. IV. Fasc. 9-10. Vol. VI. Fasc. 2-3. 1890-94. Somerville, Mass :-Tufts College. Studies. No. 1. 8vo. [Somerville] 1894.

The College.

Toulouse :-Académie des Sciences, Inscriptions et Belles-Lettres. Mémoires. Tome V. 8vo. Toulouse 1893.

The Academy.

Observations and Reports.

Batavia :-Magnetical and Meteorological Observatory. Observations. 1892. Folio. Batavia 1893; Rainfall in the East Indian Archipelago. 1892. 8vo. Batavia 1893.

The Observatory. Bucharest :-Institutul Meteorologic. Analele. Tom. VII. 4to. Bucuresti 1893. The Institute.

France-Service des Topographies Souterraines. Études des

Gîtes Minéraux de la France. Bassin Houillier et Permien d'Autun et d'Épinac. Fasc. 5. 4to. Paris 1893. The Service. India-Great Trigonometrical Survey of India.

Operations. Vol. XV. 4to. Dehra Dun 1893.

Account of the

Secretary of State for India. Mersey-Report on the Present State of the River Mersey. 1893. 8vo. London 1894. Adm. Sir G. H. Richards, F.R.S. Paris-Bureau des Longitudes. Connaissance des Temps. 1896. 8vo. Paris 1893; Extrait de la Connaissance des Temps. 1895. Svo. Paris 1893; Éphémérides des Étoiles de Culmination Lunaire et de Longitude. 1894. 1894. 4to.

Bureau International des Poids et Mesures.
Mémoires. Tome X. 4to. Paris 1894.

Paris 1893.

The Bureau.
Travaux et

The Bureau.

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