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connexion with a nerve-cell, which exerts over it a peculiar influence which enables it to retain its structure," &c. He does not think it proved, however, that all ganglia exert an influence both in a central and peripheral direction like those of the posterior spinal roots, and indeed experiments have shown that certain ganglia, such as the superior cervical of the sympathetic, exert their sustaining power on the nerve-fibres connected with them, in one direction only.

The investigation of the effects of section on the optic nerve, which forms the subject of the present communication, promised to yield interesting results on several grounds, and especially as calculated to throw light on the relations of the fibres of the nerve to those of the opposite one in the optic chiasma or commissure, and on the question as to the manner in which they are connected with the brain.

After some observations on the structure of the optic nerve, the author describes his experimental procedure. To see the nerve whilst operating, and thus be assured that the section was effected at the desired point, he began by dislocating the eyeball forwards from its socket, while the animal was under the influence of ether. This operation he found could be effected in the rabbit, by simply pressing the eyelids widely apart, and was unattended with any serious disturbance of the functions of the organ. In dogs the operation is more difficult, and occasions more injurious effects. When the eye is dislocated, its axis is inclined downwards and inwards, and the optic nerve can be reached without difficulty ; so that it may readily be cut at any desirable distance behind its place of entrance into the eyeball, and may even by moderate traction be broken off immediately before the chiasma.

After stating various observations which he made on the dislocated eye, the author gives an account of the effects which resulted from section of the optic nerve. The condition of the retina after the operation, was studied during the life of the animal by means of the ophthalmoscope; and, after death, its structure, as well as that of the optic nerve before and behind the place of section, the chiasma, the optic tracts, and connected part of the brain, was examined with the microscope.

The elements of the retina, as well as those of Jacob's membrane, were found unaltered four months after the time of section. The distal part of the optic nerve (that left in connexion with the eyeball), examined after the lapse of a month in one case, and of two months in another, was also discovered to be unaltered. On the other hand, the part of the nerve behind or on the central side of the section was invariably disorganized. The section was usually performed on the optic nerve of the right eye, and the disorganized fibres of its central segment could be traced back to the left optic tract, through the chiasma, where they obviously decussated with the sound fibres of the opposite nerve. The right optic tract had undergone no change; the fibres of the left tract were disorganized as far back as the quadrigeminate bodies, except those running along the posterior or inner border of the tract; which exception appears to the author to favour the opinion that fibres pass along the tracts and commissures from the quadrigeminate bodies of one side to those of the other side, without connecting themselves with the retina. On the other hand, the results of his experiments do not seem to him to countenance the notion of fibres running in the optic nerves from one retina to the other without connexion with the brain, nor the generally received doctrine that part of the fibres of the optic nerve are continuous with the optic tract of the same side; on the contrary, the whole fibres of the nerve would seem to undergo decussation.

The microscopic characters of the atrophied and disorganized nervous substance are described in the paper; they were found to differ somewhat in the part of the nerve before and that behind the chiasma, owing no doubt to the different structure of these parts in the sound state.

The changes produced in the geniculate and quadrigeminal bodies will be communicated in the succeeding part of the paper.

II. “On some of the Metamorphoses of Naphthalamine.” Ву

A. W. HOFMANN, Ph.D., F.R.S. &c. Received January

10, 1856. The great facility with which some of the nitro-hydrocarbons can be reduced by means of iron and acetic acid—the modification of Zinin's process, lately proposed by M, Béchamp-enables us to obtain the corresponding bases in larger quantity, and to examine their derivatives more minutely.

One of the bases, for the preparation of which this process is particularly applicable, is naphthalidine, or as it is more appropriately called, naphthalamine. Mr. William H. Perkin is engaged in examining the deportment of this substance with chloride of cyanogen, and the following is a summary of the results he has at present obtained.

Fused naphthalamine, when submitted to the action of chloride of cyanogen, absorbs this gas with great avidity, and is gradually converted into a dark resinous mass. This is the hydrochlorate of a new base, which has received the name of menaphthalamine, in consequence of the analogy of its origin with that of melaniline, derived by a similar process from aniline.

Menaphthalamine is separated from the hydrochlorate by potassa, washed and repeatedly recrystallized from alcohol. It contains

C4, H, N3, nd is formed according to the equation

2C20 H, N + C, NCI = C, H,,N, HCI.

Naphthala- Chloride of Hydrochlorate of

mine. cyanogen. menaphthalamine. Mr. Perkin has verified this formula of menaphthalamine by the analysis of the hydrochlorate and of the platinum salt, which respectively contain

C4, H,, N2, HCl and

C4, H, N3, HCI, PtCl . Among the various metamorphoses which menaphthalamine undergoes under the influence of agents, the deportment of this substance with cyanogen has especially engaged the attention of Mr. Perkin.

Menaphthalamine, like melaniline, absorbs two equivalents of cyanogen, and is converted into a slightly crystalline buff-coloured substance, which retains feebly basic properties.

The analysis of this body, which, from its composition, may be termed dicymenaphthalamine, has led to the formula

C46 H, N, = C, H, N, + Cyg.

Dicymenaphthalamine is insoluble in water, moderately soluble in alcohol and ether. It dissolves readily in acids. The latter solution, when precipitated by potassa, immediately after it has been made, yields unchanged dicymenaphthalamine; but if the solution be allowed to stand for a few moments, a yellow substance is precipitated, which is no longer a salt of dicymenaphthalamine.

The composition of this yellow body, which, in accordance with the terminology adopted in the aniline series, may be called menaphthoximide, is represented by the following formula

C46 H15 N,00 and its formation is illustrated by the equation-

C46 HN, + 4H0 + 2HCl = C46 H15 N, 04 + 2NH, CI.

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In fact, the mother-liquor of this substance contains a large amount of ammonia.

Menaphthoximide may be viewed as binoxalate of menaphthalamine minus 4 equivalents of water

C42 H , N, HC,04, HC,04 - 4H0 = C46 H76 N204

4 ;

: Binoxalate menaphthalamine.


and this view is corroborated by the deportment of the substance with potassa, which reproduces menaphthalamine and oxalic acid.

From the preceding experiments, it is obvious that the deportment of naphthalamine with chloride of cyanogen is perfectly analogous to that of aniline. The subsequent metamorphoses of the newly-formed compound also exhibit the same analogy.

Aniline series.

Naphthalamine series. Aniline...... C, H, N Naphthalamine ... C20 H, N Melaniline .. CH13 Ng Menaphthalamine Dicymelaniline C30 H13 N, Dicymenaphthalamine C 46 H1,7 N, Melanoximide C3 1,3 1,04 Menaphthoximide C46 H, N, 04

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Results of much interest are to be expected from the examination of the products formed by the action of heat on menaphthoximide.

It is probable that this reaction would produce the naphthalamine
term, corresponding to anilocyanic and cyanic acid.
Cyanic acid....

C, H NO,
Anilocyanic acid..

C14 H. NO, Naphthocyanic acid ...... C, H, NO, Menaphthoximide, when heated, yields, in fact, a vapour of a most penetrating organic odour ; but Mr. Perkin has not yet obtained sufficient material for a more minute examination of the body to which it belongs.

January 24, 1856.

Sir BENJAMIN BRODIE, Bart., V.P., in the Chair.

A paper was in part read, entitled “Account of Pendu.

lum Experiments undertaken in the Harton Colliery for the purpose of determining the Mean Density of the Earth.” By G. B. AIRY, Esq., Astronomer Royal. Received December 26, 1855.

January 31, 1856.

The LORD WROTTESLEY, President, in the Chair.

The reading of Mr. Airy's paper, entitled “ Account of

Pendulum Experiments undertaken in the Harton Colliery for the purpose of determining the Mean Density of the Earth,” was resumed and concluded.

(Abstract.) In the first section of this paper, the anthor explains the reasons, founded on calculation, which appeared to make it probable that the comparison of gravity at the top and the bottom of a mine

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