INHERITED MUTILATIONS.

The almost universal _non-inheritance_ of mutilations seems to me a far

more valid argument _against_ a general law of modification-inheritance

than the few doubtful or abnormal cases of such inheritance can furnish

in its favour. No inherited effect has been produced by the docking of

horses' tails for many generations, or by a well-known mutilation which

has been practised by the Hebrew race from time immemorial. As lost or

mutilated parts are reproduced in offspring independently of the

existence of those parts in the parent, there is the less reason to

suppose that the particular condition of parental parts transmits

itself, or tends to transmit itself, to the offspring. So unsatisfactory

is the argument derivable from inherited mutilations that Mr. Spencer

does not mention them at all, and Darwin has to attribute them to a

special cause which is independent of any general theory of

use-inheritance.[54]

Darwin's most striking case--and to my mind the only case of any

importance--is that of Brown-Sequard's epileptic guinea-pigs, which

inherited the mutilated condition of parents who had gnawed off their

own gangrenous toes when anaesthetic through the sciatic nerve having

been divided.[55] Darwin also mentions a cow that lost a horn by

accident, followed by suppuration, and subsequently produced three

calves which had on the same side of the head, instead of a horn, a bony

lump attached merely to the skin. Such cases may seem to prove that

mutilation _associated with morbid action_ is occasionally inherited or

repeated with a promptitude and thoroughness that contrast most

strikingly with the imperceptible nature of the immediate inheritance of

the effects of use and disuse; but they by no means prove that

mutilation in general is inheritable, and they are absolutely no proof

whatever of a _normal_ and non-pathological tendency to the inheritance

of acquired characters. Those who accept Darwin's special explanation

of the supposed inheritance of mutilations, ought to notice that his

explanation applies equally well under a theory which is strongly

adverse to use-inheritance--namely, Galton's idea of the sterilization

and complete "using up" of otherwise reproductive matter in the growth

and maintenance of the personal structure.

Darwin's explanation of inherited mutilations--which, as he notes, occur

"especially or perhaps exclusively" when the injury has been followed by

disease[56]--is that all the representative gemmules which would develop

or repair or reproduce the injured part are attracted to the diseased

surface during the reparative process and are there destroyed by the

morbid action.[57] Hence they cannot reproduce the part in offspring.

This explanation by no means implies that mutilation would _usually_

affect the offspring. On the contrary, in all ordinary cases of

mutilation the purely atavistic elements or gemmules would be set free

from any modifying influence of the non-existent or mutilated part. The

gemmules--as in Galton's theory of heredity and with neuter

insects--might be perfectly independent of pangenesis and the normal

inheritance of acquired characters. Such self-multiplying gemmules

without pangenesis would enable us to understand both the excessive

weakness or non-existence of normal use-inheritance, and the excessive

strength and abruptness of the effect of their partial destruction under

special pathological conditions.

The series of epileptic phenomena that can be excited by tickling a

certain part of the cheek and neck of the adult guinea-pig during the

growth and rejoining of the ends of the severed nerve, are said to be

repeated with striking accuracy of detail in the young who inherit

mutilated toes; but as epilepsy is often due to some _one_ exciting

cause or morbid condition, the single transmission of a highly morbid

condition of the system might easily reproduce the whole chain of

consequences and might also have caused the loss of toes.

The particulars of the guinea-pig cases are very inadequately

recorded,[58] but the results are so anomalous[59] that Brown-Sequard's

own conclusion is that the epilepsy and the inherited injuries are

_not_ directly transmitted, but that "what is transmitted is the morbid

state of the nervous system." He thinks that the missing toes may

"possibly" be exceptions to this conclusion, "but the other facts only

imply the transmission of a morbid state of the sympathetic or sciatic

nerve or of a part of the medulla oblongata." Until we can tell what is

transmitted, we are not in a position to determine whether there is any

true inheritance or only an exaggerated simulation of it under peculiar

circumstances. When the actual observers believe that the mutilations

and epilepsy are not the cause of their own repetition, and when these

observers guard themselves by such phrases as, "if any conclusion can at

present be drawn from those facts," we who have only incomplete reports

to guide us may well be excused if we preserve an even more pronounced

attitude of caution and reserve.[60] The morbid state of the system may

be wholly due to general injury of the germs rather than to specific

inheritance.

Weismann suggests that the morbid condition of the nervous system may be

due to some infection such as might arise from microbes, which find a

home in the mutilated and disordered nervous system in the parent, and

subsequently transmit themselves to the offspring through the

reproductive elements, as the infections of various diseases appear to

do--the muscardine silkworm disease in particular being known to be

conveyed to offspring in this manner.

But whether we can discover the true explanation or not, inherited

mutilations can hardly be accounted for as the result of a general

tendency to inherit acquired modifications. How could a factor which

seems to be totally inoperative in cases of ordinary mutilation, and

only infinitesimally operative in transmitting the normal effects of use

and disuse, suddenly become so powerful as to completely overthrow

atavism, and its own tendency to transmit the non-mutilated type of one

of the parents and of the non-mutilated type presented by the injured

parent in earlier life? Does not so striking and abrupt an

intensification of its usually insignificant power demand an explanation

widely different from that which might account for the extremely slow

and slight inheritance of the normal effects of use and disuse? Surely

it would be better to suspend one's judgment as to the true explanation

of highly exceptional and purely pathological cases rather than resort

to an hypothesis that creates more difficulties than it solves.

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