To come to the limbs, we find the _shoulder-blade_ presenting three

_epiphyses_, one for the _coracoid_ process, one for the _acromion_, and

one for the lower angle of the bone, the ossification of which begins

soon after puberty, their union with the body of the bone taking place

between the ages of twenty-two and twenty-five years. The _clavicle_ has

an _epiphysis_ at its sternal end, which begins to form between the

eighteenth and twentieth years, and is united to the rest of the bone a

few years later. The consolidation of the shoulder-bone (_humerus_) is

completed rather earlier; the large piece at the upper end, which is

formed by the coalescence of the ossific centres of the head and two

tuberosities, unites with the shaft at about the twentieth year; whilst

its lower extremity is completed by the junction of the external

condyle, and of the two parts of the articulating surface (previously

united with each other), at about the seventeenth year, and by that of

the internal condyle in the year following. The superior _epiphyses_ of

the arm-bones (_radius_ and _ulna_) unite with their respective shafts

at about the age of puberty; the inferior, which are of larger size, at

about the twentieth year. The _epiphyses_ of the _metacarpal_ and

_phalangeal bones_ (those of the hand and fingers) are united to their

principals at about the twentieth year. In the _Lower Extremities_, the

process of ossification is completed at nearly the same periods as that

of the corresponding parts of the Upper. The consolidation of the

hipbones (_ilium_, _ischium_, and _pubis_) to form the _os innominatum_,

by the ossification of the triradiate cartilage that intervenes between

them in the socket of the thigh (_acetabulum_), does not take place

until after the period of puberty; and at this time additional

_epiphyses_ begin to make their appearance on the crest of the _ilium_,

on its anterior inferior spine, on the tuberosity of the _ischium_, and

on the inner margin of the _pubes_, which are not finally joined to the

bone until about the twenty-fifth year.[88]

The concurrence of these conditions in the skeleton, the nearly balanced

ratio of the bloods, the perfected dentition, the beard, the deepened

voice, the prominent larynx, and the stature, combine to point out,

with infallible precision, the age of this Man, as between twenty-five

and thirty years.

So far, then, we can with certainty trace back the history of this

being, as an independent organism; but did his history then commence? O

no; we can carry him much farther back than this. What means this

curious depression in the centre of the abdomen, and the corrugated knob

which occupies the cavity?[89]

This is the NAVEL. The corrugation is the cicatrice left where once was

attached the umbilical cord, and whence its remains, having died,

sloughed away. This organ introduces us to the foetal life of Man;

for it was the link of connexion between, the unborn infant and the

parent; the channel, through whose arteries and veins the oxygenated and

the effete blood passed to and from the parental system, when as yet the

unused lungs had not received one breath of vital air.

And thus the life of the individual Man before us passes, by a necessary

retrogression, back to the life of another individual, from whose

substance his own substance was formed by gemmation; one of the

component cells of whose structure was the primordial cell, from which

have been developed successively all the cells which now make up his

mature and perfect organism.

* * * * *

How is it possible to avoid this conclusion? Has not the physiologist

irrefragable grounds for it, founded on universal experience? Has not

observation abundantly shown, that, wherever the bones, flesh, blood,

teeth, nails, hair of man exist, the aggregate body has passed through

stages exactly correspondent to those alluded to above, and has

originated in the uterus of a mother, its foetal life being, so to

speak, a budding out of hers? Has the combined experience of mankind

ever seen a solitary exception to this law? How, then, can we refuse the

concession that, in the individual before us, in whom we find all the

phenomena that we are accustomed to associate with adult Man, repeated

in the most exact verisimilitude, without a single flaw--how, I say, can

we hesitate to assert that such was his origin too?

And yet, in order to assert it, we must be prepared to adopt the old

Pagan doctrine of the eternity of matter; _ex nihilo nihil fit_. But

those with whom I argue are precluded from this, by my first Postulate.

XI.

PARALLELS AND PRECEDENTS.

(_Germs._)

"Every cell, like every individual Plant or Animal, is the

product of a previous organism of the same kind."--(DR.

CARPENTER, _Comp. Physiol._ Sec. 347.)

In the preceding examples I have assumed that every organic entity was

created in that stage of its being which constitutes the acme of its

peculiar development; when all its faculties are in their highest

perfection, and when it is best fitted to reproduce its own image. From

the very nature of things I judge that this was the actual fact;[90]

since, if we suppose the formation of the primitive creatures in an

undeveloped or infant condition, a period would require to lapse before

the increase of the species could begin; which time would be wasted. To

those, indeed, who receive as authority the testimony of the Holy

Scripture, the matter stands on more than probable ground; for its

statements, as to the condition of the things created, are clear and

full: they were not seeds, and germs, and eggs, and embryos,--but "the

tree yielding fruit whose seed was in itself,"--"great whales,"--"winged

fowl,"--"the beast of the earth,"--and "man."[91]

But I do not mean to shield myself behind authority. I have begged the

_fact_ of creation; but not the truth, nor even the existence, of any

historic document describing it. It is essential to my argument that any

such be left entirely out of the question; and, for the present, I

accordingly ignore the Bible.

It is possible that some opponent may object to my assumption of

maturity in created organisms.

"Your deductions may be sound enough," such an one may say, "provided

your newly-created Locust-tree had so many concentric cylinders of

timber, your Tree-fern had a well-developed stem of leaf-bases, your

Coral a great aggregation of polype-cells, your Tortoise a carapace of

many-laminated plates, your Elephant a half-worn set of molars, and your

Man a thoroughly ossified skeleton. But how do you know that either of

these organisms was created in this mature stage? I will not deny that

each was created,--was called suddenly out of non-entity into entity;

but I believe, or at least I choose to believe,--that each was created

in the simplest form in which it can exist; as the seed, the gemmule,

the ovum, the--ahem!"

Pray go on! you were about to say "the infant," or "the foetus," or

"the embryo," probably; pray make your selection: which will you say?

"Well, I hardly know. Because, if I choose the new-born infant, you will

say, Its condition implies a nine months' pre-existence, certainly; not

to speak of the absurdity of a new-born infant being cast out into an

open world without a parent to feed it. If I say, The foetus, or the

still more incipient embryo, I involve, at once, a pre-existent mother.

I am afraid you have me there!"

I think I have. However, let us take up the matter orderly, and proceed

on the supposition that my previous examples must be all cancelled, and

the question argued _de novo_, on the assumption that each organism was

created in its least developed condition.

It will not be considered necessary, I suppose, to look at any

intermediate condition of the organisms. The argument which is based

upon the leaf-scales of the Fern or the Palm would essentially apply to

either of these plants when it first issues from the ground. At the

period when it comprises but a single frond, the botanist would no more

hesitate in pronouncing that the organism had passed through stages

previous to that one, than he would when it possesses an elongated

stipe; though, in the latter case, the evidences of the pre-existence

are more patent to the uninstructed eye. He would say, The single frond

implies, with absolute necessity, a spore in the one case, a seed in the

other; and we need not to see either, to be assured that this must have

preceded the leaf-stage.

But you go farther back still. "The plant was created as a seed." Let us

renew our imaginary tour at the epoch, or epochs (as many as you

please), of creation, on this supposition.

Here is a very young plant of the curious Seychelles Palm or Double

Cocoa-nut (_Lodoicea Sechellarum_). A single frond is all that is yet

developed, and this is as yet unexpanded, the pinnae being still folded

on the midrib, like a fan. Trace the frond down to its base. It springs

from a thick horizontal cylindric process, which has also shot down a

radicle into the soil. We trace the cylindrical stem along the surface

of the soil, and find, lying on the ground, among the grass, but not

buried, a great double nut, something like the two hemispheres of a

human brain, or like a common cocoa-nut, half split open and healed. Out

of this the thick stem has issued; and we find that it is only the

cotyledon of the seed, that has prolonged its base in the process of

germination, in order to throw up, clear of the nut, the plumule and

radicle.

We look at the great nut, and find, on the woody exterior of the fibrous

pericarp, at the side opposite to that whence issues the cotyledon, a

broad scar. What is this? It is the _mark left by the severance of a

footstalk_, which united the fruit to the parent plant. This great drupe

was once a small ovary seated in the centre of a three-petaled flower,

which, with many others, issued out of a great spathe, a mass of

inflorescence, and hung down from the base of the leafy coronal of an

adult palm-tree. This scar is an irreproachable witness of the existence

of the parent palm.

Here, lying on the dry and dusty earth, is a brown flat bean of great

hardness. This is a seed destined by and by to produce that splendid

tree _Erythrina crista-galli_. But it has been just created.

This bean bears on one of its edges an oval scar, very distinctly

marked, called the _hilum_. This was the point of attachment of a short

column, by which the seed was united to one of the sutures of a long

pod, in the interior of which it lay, in company with several others

like itself. This great legume or pod had been the bottom of the pistil

of a papilionaceous flower, crowned by a tiny stigma, lodged in a sheath

formed by the united stamens, and surrounded by a corolla of refulgent

scarlet petals.

Of course such a flower was not an independent organism; it was one of

many that adorned a great tree, the history of whose life would carry us

back through several generations of human years.

[Illustration: GARDEN TULIP.

Fig. 1. A flower with two petals removed, to show the ovary, _a_. Fig.

2. The same ovary, more mature, divided longitudinally; _b_, the unripe

seeds, packed on each other; _c_, a portion of the same carpel, from

which the seeds have been removed.]

This single infolding leaf, that is just shooting from the soil, so

small and feeble,--what of this? There are certainly no concentric

cylinders of timber here: can we trace a previous history of this?

Yes: by carefully removing the soil from the base, we see that it

originates in a flat yellow seed--the seed of a Tulip. Here again we

have no difficulty in detecting evidence of its former attachment. A

great number of these seeds were once closely packed one on another, in

each of the three carpels that constituted the capsule. And this capsule

had been the oblong, three-sided ovary, which formed the body of the

pistil in some beautiful Tulip.

Do you observe these two round fleshy leaves, just peeping from the

sandy earth? They are the earliest growths of a plant of _Arachis

hypogaea_. In this case again, to understand the true relations of this

organism, we must expose it wholly to view.

Beneath the surface of the earth, then, I find that these seed-leaves

are the two halves (_cotyledons_) of a kind of pea, which was formerly

enclosed in a wrinkled skinny pod. But what is most interesting is that

the pod is here, the cotyledons shooting out of it. And, attached to

one end of the pod, here is a slender stalk, now withered and dry, which

projects out of the ground into the air.

[Illustration: GERMINATION OF EARTH-PEA.]

Now here we have a beautiful link of connexion with the past. The plant

before us does not ripen its seeds, and then drop them to care for

themselves, as most plants do. "The young fruit, instead of being placed

at the bottom of the calyx, as in other kinds of pulse, is found at the

bottom and in the inside of a long slender tube, which looks like a

flower-stalk. When the flower has withered, and the young fruit is

fertilized, nothing but the bottom of the tube with its contents

remains. At this period a small point projects from the summit of the

young fruit, and gradually elongates, curving downwards towards the

earth. At the same time the stalk of the fruit lengthens, until the

small point strikes the earth, into which the now half-grown fruit is

speedily forced, and where it finally ripens in what would seem a most

unnatural position."[92]

The young plant before us has been this moment created, and created in

this incipient stage of growth: and yet there is, even here, an

indubitable evidence, so far as physical phenomena can afford it, of a

past history. It would be utterly impossible to select any stage in the

life of the Earth-pea, which did not connect itself, visibly and

palpably, with a previous stage.

Let us return to the shore-loving Mangrove. You object to my assumption

that it was created as a tree, with a well-branched stem elevated upon

a series of arching roots; and to my deduction of pre-lapsed years for

the formation of those roots. Very well. I give it up. You allow that

the primitive Mangrove was created in some stage, but you contend for

the germ-stage, the simplest condition of the plant, whatever that might

be.

Now, where shall we find it? In the first pair of developed leaves? They

certainly point back to the cotyledons. To the cotyledons, then, let us

look.

Lo! the young plant is germinating before its connexion with the parent

is severed. It is the singular habit of this tree, that its seeds are

already in a growing condition, while they hang from the twig. Each seed

is a long club-shaped body, with a bulbous base and a slender point,

more or less produced. While it yet hangs from the branch, the radicle

and crown of the root begin to grow, and gradually lengthen, until the

tip reaches the soil, which it penetrates and thus roots itself; while

those which depend from the higher branches, after growing for a while,

drop, and, sticking in the mud, throw out roots from one end, and leaves

from the other.

[Illustration: SEED OF MANGROVE.]

What have you gained, then, in this case, by going back to the germ? The

germ as decisively asserts its origination from an already existing

organism--the parent tree--as the flourishing tree witnesses its gradual

development from a germ. The Mangrove could not by possibility have been

created in any stage, consistent with the identity of the species with

that which we behold now in the nineteenth century,--that did not show

ocular evidence of a previous history;--evidence from the nature of

things fallacious.

It would be merely tiresome to go on through the vegetable kingdom. In

every plant the simplest condition--viz. that of a spore or

seed--depends on some development, or process, or series of processes,

that have preceded it. Nor does the lapse of time between the previous

process and the apparent result at all destroy their necessary

connexion. In the case of the curious Misseltoes, the ovule does not

appear till three months after the pollen has been shed; but when it

does appear, its existence as an organism capable of developing the

characteristic form of its species, is as truly dependent on the

previous existence of the pollen, as if not an hour had intervened.

Supposing the essential conditions of vegetable organisms to have been

at the first what they are now; in other words, supposing specific

identity to have been always maintained,--which I have demanded as a

postulate for this argument,--it appears to me demonstrable, that every

plant in the world presented at the moment of its creation evidences

_prochronic_ development, in nowise to be distinguished from those on

which we firmly rely as proving the lapse of time.

But is the case otherwise in the animal world?

We traced back the history of our Medusa through its marvellous series

of gemmative developments, till we reached the minute Infusory-like

gemmule, which is its simplest form. Now it is quite legitimate to

assume that _this_, and not the pulmonigrade umbrelliform stage, was the

one in which the new-created Medusa began existence. Have we, then, got

rid of the evidence of past time, which we deduced from the successive

changes through which the adult had passed? What is this ciliated

planule, and whence comes it? It is the embryo discharged from the

fringed ovary of a female Medusa; it has already passed through several

changes of colour and form. It is now of a deep yellow colour; it has

been violet; it has been colourless: it is now shaped like a dumb-bell;

it was a globule; it had been a mulberry-mass. Yet earlier, it had been

a component cell of the ovarian band, which divided the generative

cavity from that of the stomach, in the parent Medusa.

In like manner the ciliated gemmule from which was formed the "pluteus"

of the Urchin, was dependent on the existence of a parent Urchin; the

monadiform germ from which was developed the pentacrinus of the

Feather-star, was originally hidden in the ovarian tubes of a parent

Feather-Star: the infant _Serpula_ that deposited the first atoms of

calcareous matter as a commenced tube, had begun its own existence in

the body of a parent _Serpula_.

It is true the evidence of the connexion between the germ and the

parent is not in these low forms always patent to the eye; it is

physiological. But it is not less conclusive to one who is able to

appreciate its force. A physiologist is as sure that every germ, every

ovum, in the Invertebrate animals, was produced by an animal of a former

generation, as he is of the same fact in a Mammal, where his eye can see

the scar of the umbilical cord.

In many instances there is stronger, or rather more obvious and

ordinarily appreciable, evidence of the link between the present and the

past generation, than the physiological dependence. The world of

Insects, which, from its immensity, and from the high organic rank of

its members, affords us so exhaustless a mine of economical wonders,--is

rich in examples to the point. A few of these I shall cite.

The eggs of many Insects are not dropped anywhere, at random; for, as

the newly-born young have limited powers of locomotion, and yet are in

general able to subsist only on some particular kind of food, it is

necessary that their birth should occur in the immediate proximity of

such food: and therefore that the egg should be so placed. Now this

circumstance would not be specially noteworthy if the locality selected

for the deposition of the egg were the same as that in which the parent

insect had been accustomed to find its own private enjoyments: we should

reasonably say that the eggs were placed here, because the parents

happened to be here. The case, however, is very different.

We never find the egg of the Peacock Butterfly adhering to the leaf of a

cabbage, nor that of the Garden White to the leaf of a nettle; but the

nettle is invariably selected for the former, and a cruciferous plant

for the latter.

Yet there is nothing in the individual wants or likings of the

Butterfly, in either case, to account for this. Both the one and the

other flutter through the sunny air, alight to drink the water of some

slushy pool, rest on the expanding flowers and probe them for nectar, or

suck the exuding juices of an over-ripe fruit. But when did you ever see

the gorgeous-eyed Peacock feeding on a nettle, or the White on a

cabbage? Eagerly as they seek these plants, it is solely for the purpose

of depositing their eggs where instinct teaches them their unborn

progeny will find suitable food.

Supposing, therefore, we had found the egg of either of these

butterflies at the moment of its creation, we should assuredly have

found it on the nettle or the cabbage (as the case might be); because to

suppose it in any other situation would be equivalent to supposing it so

placed as that the end of its creation--the life of the species

created--would be _ipso facto_ frustrated. But, finding it so, the

question naturally arises,--Why here, and not elsewhere? and the only

possible answer, on the ground of phenomena, is, Because the parent

chose this situation for it. And thus we are inevitably thrown back to

an anterior generation, which is equivalent to past time.

Again, if we had seen the egg of the Nut Weevil (_Balaninus nucum_) just

come from the creative hand of God, we should certainly have found it

within the immature soft-shelled hazel-nut, because there alone would

the grub when hatched meet with "food convenient for" it. And yet if we

had sought (ignorant of the fact of its recent creation) the reason of

its being there, our acquaintance with entomology would have pointed to

the parent beetle, who, with her jaws placed at the tip of a long

slender snout, had bored a tiny hole in the tender shell, and had then

projected the egg from her abdomen into the interior.

The eggs of the _Oestridae_--for example, the Worble of the Ox

(_Oestrus bovis_) or the Bot of the Sheep (_Oe. ovis_)--would be

discovered in no other circumstances than beneath the skin of the

former, and at the edge of the nostrils of the latter. For these are the

respective situations in which the egg is always deposited, that of the

Worble hatching _in situ_, and forming a superficial abscess in

communication with the external air, and that of the Sheep-bot producing

a larva which crawls up the nostrils of the poor animal, till it finds a

suitable resting-place in the frontal sinuses of the skull. To suppose

the egg in any other circumstances than those which I have mentioned,

would be to consign it to certain destruction. Yet does not its presence

there bear witness to the eclectic care of the parent Gadfly, whose

unerring instinct knew how to seek and select the right position?

If you had set yourself to look for the egg of a _Pimpla manifestator_,

a common Cuckoo-fly, where would you have looked for it, but in the

fatty tissues of a wild bee's grub, that was lodged in a deep hole in

some old post? If you had sought elsewhere, you would surely have been

disappointed. And would not its presence there bear testimony to the

lengthened ovipositor of the well-known brisk and busy fly, and to its

remarkable habits?[93]

The grub of the Pill Chafer or Tumble-dung Beetle (_Phanaeus_) feeds on

the ordure of _Mammalia_. And, in order that the newly-hatched young may

have a copious supply of food at hand, the parent chafer with its jaws

detaches a mass of recent ordure, which it then rolls over the ground

with its hind feet, until it acquires a globular form, and a coating of

earth or sand. An egg is then deposited in the centre of the ball, which

is rolled into a hole made in the earth to receive it. The coating of

earth drying and hardening, keeps the interior of the mass fresh and

moist until the young grub is hatched, when it at once begins to devour

its savoury and delicate provision.

It would be vain to search for the egg of a _Cynips_ except within a

vegetable gall, or at least within the tissues of a plant that are going

to produce one. Take as an example _C. quercus_, which produces the

spongy excrescence well known as the common Oak-apple. The female

Gall-fly is furnished with an ovipositor in the shape of a very fine

curved needle, with which she punctures the tender bark of an oak shoot,

lodging an egg in the perforation. Stimulated by some fluid, probably,

which is poured into the wound at the same time, the sap forms a

peculiar tissue around the egg, swelling into a large ball, on which the

young grub begins to feed eagerly, and in which it finds the only

nutriment on which it could subsist.

Now, if we had found the egg of a Gall-fly newly created, we should

certainly have found it in a gall; and the gall would have afforded us

indubitable evidence of the wounding of the vegetable tissues, and of

the organ, secretion, and instinct of the tiny fly by which the process

had been effected. The evidence would be irresistible, but of course it

would be fallacious.

Let us now look at a few examples in which the egg is found in

invariable association not merely with something that the parent has

found for it, but with something that has proceeded from her, a part of

herself.

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