that he passed from an ancestral, quadrupedal condition, through the
semi-erect to his present upright posture, slowly and laboriously. His
erect attitude, geologically speaking, is a very recent accomplishment,
and his anatomy, therefore, reveals many imperfect adaptations to his
newly acquired posture. These imperfect adaptations are the sources
of many grave diseases in mankind. It would require too technical a
knowledge of anatomy to explain these imperfect adaptations, and I will
therefore simply mention _rupture_ and _uterine displacements_ as due to
imperfect adaptations to the upright attitude.
The common origin of man and the ape accounts for many interesting
and otherwise inexplicable facts in anatomy. There is, for instance,
a muscle that is normally present in the orang-outang known as the
Opponens Hallucis. This muscle enables the orang to oppose his big toe
to the other toes, just as we can oppose our thumb to the other fingers
of our hand. This muscle is absent from the foot of man ordinarily. But
occasionally it is found in man, in the dissecting-room, as a rarity—as
an anomaly. The question naturally arises, why should this muscle be
present normally in the orang and absent normally in man, occurring in
the latter only as an abnormality? The theory of evolution gives the only
rational answer. The man-like, ape-like generalized ancestors of man and
the orang possessed this muscle, which was useful to them in grasping
the branches of the trees among which they lived. These ancestors used
the feet and hands alike for purposes of grasping (prehension) and
locomotion. But those descendants that evolved more and more man-ward
used the feet more for purposes of locomotion and less for grasping,
while they used the hands more for grasping and less for locomotion,
until, finally, man was created—a creature that uses his feet exclusively
for locomotion, and the hands entirely for grasping. Through disuse,
therefore, the _opponens hallucis_ gradually disappeared in man; so that
now it occurs only as a rare abnormality. The hereditary units that make
this muscle still lie dormant in most men are usually so weak, through
disuse, that they do not develop. Some unusual stimulus occasionally
causes the latent hereditary units to develop and makes it appear in man.
The same is the case with many other muscles and structures that are
normal in the modern anthropoid apes, and only occur as rarities in man.
The appearance of those muscles in man are instances of _atavism_, i. e.,
reversions to conditions that were normal in the ancestors of man and the
apes, as they are still normal in the latter.
USELESS SCAFFOLDING LEFT IN THE BODY.
Man, in his post-natal growth, as well as during his embryological
development, exhibits reminiscences of his animal ancestry. In the
structure and movement of the new-born babe, as well as in the adult
frame, we find continuous witnesses to the ancient animal strain.
On the theory that men in bygone ages were closely allied to simian
creatures in habit as well as structure; that they led an arboreal life;
and that, like the baby-monkeys to-day, the baby-men of other ages clung
to their mothers as they climbed among the trees, Dr. Louis Robinson
predicted that a =baby’s power for grasping= would likely be found to
equal that of a young monkey which had reached a corresponding period
of growth. He tested a large number of new-born infants in reference to
this power by extending his finger or a cane, to imitate the branch of
a tree, and observed how long they would hang there without any other
support (Plate XI). He made experiments on about sixty children under
a month old. About thirty of the children experimented upon were not
over an hour old. Dr. Robinson states that each of the infants, with two
exceptions, was able to hang to the finger or cane by its hands, like
an acrobat from a horizontal bar, and sustain the whole weight of its
body for at least ten seconds. Twelve of the infants, less than an hour
old, held on for half a minute before the grasp relaxed; while four of
this age held on for one minute. Over fifty of the infants when four
days old could continue the grip for half a minute. Three weeks after
birth the faculty for holding on reached its maximum, for at this age
several succeeded in hanging on for a minute and a half; two held on for
over two minutes; and one infant held on over two minutes and a half.
One infant that was less than an hour old hung by both hands to Dr.
Robinson’s finger for ten seconds, and then deliberately let go with his
right hand, as if to seek a better hold, and continued his grasp with the
left hand only, for five seconds longer. In none of these experiments
did the limbs of the infants hang down in the attitude of the erect
position, but the thighs were invariably in the baby-monkey attitude,
at right angles to the body. The doctor says that this attitude and
the disproportionately large development of the arms compared with the
legs give the photographs of the infants a striking resemblance to a
well-known picture of the celebrated chimpanzee, Sally, at the Zoölogical
Garden in London. In these experiments the infants very seldom gave any
sign of distress, and uttered no cry until the grasp began to give way.
The fact that the flexor muscles of the forearm of a new-born infant show
such remarkable strength while the other parts of the muscular system
are so conspicuously weak and flaccid,—that they are able to perform a
feat of muscular strength that will tax the powers of many a healthy
adult,—can be explained only on the theory of inherited instinct from
simian ancestors that lived in trees. This instinct is no longer useful
to an infant. It is a vestigial instinct, a useless scaffolding in its
life history.
[Illustration: PLATE XI.—Illustrating the grasping power of infants. Two
infants, ten and thirteen days old, respectively, supporting their weight
by the hands only (vestigial instinct.) Reproduced from a photograph
taken by Dr. Louis Robinson. By courtesy of the Open Court Publishing
Company.]
=Club-foot.= There is an ordinary case of malformation in the foot of a
child known as club-foot. The most common kind of this deformity is that
where the sole is turned inwards and upwards and the heel is raised.
Before birth all children pass through this condition as a perfectly
normal and natural one, and only gradually outgrow it (evolve beyond it).
But some children fail to evolve beyond this condition and have club-feet
throughout life, unless relieved by the surgeon. It is a very instructive
fact that this particular form of club-foot is the normal condition
of the adult gorilla and orang-outang. The foot of every child passes
through this gorilla phase, and if it does not develop beyond this phase
it retains the simian characters, and we call it an abnormality. In this
abnormality the anatomist finds that those bones that enter into the
formation of the ankle joint have the pronounced anatomical characters of
the adult orang-outang.
=Ribs.= Adult man possesses twelve pairs of ribs. The chimpanzee and
gorilla possess fourteen pairs. An older comparative anatomy predicted
that in an early embryonic condition man would be found to possess
thirteen or fourteen pairs. The prophecy has been verified.
=Hair.= The apes have hair over the entire body. At the sixth month
of the embryonic development the human fœtus is thickly covered with
a somewhat long, dark hair over all the body, except those parts that
are uncovered in the apes, viz.: the palms of the hands and the soles
of the feet. This covering of hair is called lanugo. Since it covers
all the body except the points noted, it extends, of course, all over
the ears, face and forehead. It is usually shed before birth. It is a
simian characteristic, and sometimes fails to disappear, but persists
and develops greatly. Therefore there are occasionally found such men
(“dog-faced men”) as the Russian Jeftichjeff. The Ainos of one of the
Japanese Islands also possess this extreme hairiness.
=Vermiform Appendix.= There are a number of vestigial structures in man
that are not only useless but even a menace to life. The most striking
of the vestigial structures that come under this category is a portion
of man’s large intestine which is called the Appendix Vermiformis. This
useless structure is a veritable death trap. In some animals, such as the
herbivorous ones, the appendix is very large, sometimes longer than the
body itself, and is of great use in digestion. But in man it has shrunken
to a small rudiment varying from two to six inches in length, which is
very liable to a grave form of disease that frequently causes death
unless timely treated by the surgeon. In the early embryo the appendix is
equal in caliber to the rest of the bowel, but at a certain date ceases
to grow _pari passu_ with it. At birth it has become a small rudiment of
the large intestine. In the new-born infant the appendix is often of the
same size as it is in the adult. This precocity of an organ is always an
indication that it was of great importance to the ancestors of the human
species.
=Tail.= Man, like the anthropoid apes, has no external tail; but, exactly
like them, he has a rudimentary one concealed beneath the skin. The
embryos of man and the ape at an early stage of growth possess a very
conspicuous tail, which is even longer than the limbs. In the embryo
of man even the muscles for wagging the tail are still found. In the
adult man these muscles are represented, normally, by bands of fibrous
tissue. In the dissecting-room one occasionally finds these muscles well
developed in the adult man. Man and the anthropoid apes have descended
from more primitive simian ancestors that possessed tails.
=Hearing.= Prominent among vestigial structures, though less easy for
beginners to understand, are those that point to piscine ancestors and
which, therefore, smack of the sea. Embryology points indubitably to the
fact that the ancient, geologic progenitors of man once lived a marine
life. In the history of the globe there was a time when all the animals
lived in the sea. Land animals appeared as later creations. Man, in
evolving from the primitive protozoan, passed through a marine-worm phase
and finally, through the ages, attained to the fish stage. The chief
characteristic of a fish is its apparatus for breathing the air dissolved
in the water. This apparatus consists of gills—strong bars with delicate,
highly vascular, fringe-like curtains hung on them, and through which the
blood is continually circulating. The circulating blood throws out its
impure gases and takes in from the water the pure air, thus breathing.
These bars or arches are five or seven in number in many fishes. Slits
extend from the surface of the fish between the bars to the throat, so
that the water which the fish takes into its mouth is forced out between
the bars, thus bathing the delicate curtains on them by which air is
breathed from the water. Sometimes the slits between the bars are open
and unprotected, as in the sharks; but in the modern fishes (teleosts)
they are protected by a lid (operculum). If these slits did not exist in
the neck all fishes would quickly perish. They are of so great use to
the fish that Natural Selection has taken exceptional care in perfecting
their mechanism.
It is one of the most interesting facts in evolution that these slits
in the fish’s neck are still represented in the neck of man. One of the
most prominent features in every mammalian embryo is the presence of four
clefts of the old gill-slits. So persistent are these characters that
children are occasionally born with persistent fissures leading to the
throat, so that milk, when swallowed, will come out on the neck through
an opening. Thus we have a persistent piscine characteristic as an
abnormality in the child.
When the fish-like ancestors of man left the water the elaborate
breathing apparatus was no longer needed for respiration. Nature, in
creating new adaptations for the land animal, did not discard the
elaborate gill apparatus that had been evolved through the ages;
but utilized this old apparatus for the new adaptations. Nature is
exceedingly economical and does not discard old organs when they can be
molded for new functions.
In the course of ages, through minute gradations, the first gill-slit and
portions of its adjacent bars were molded for purposes of hearing. In
man there are two passages leading to the drum or middle ear; one is the
external auditory canal (the opening which is seen in what is popularly
called the ear), and the other is a canal leading from the throat to the
middle ear. In the adult these two channels are partitioned off from
each other by the membrane of the drum. These canals are the counterpart
or homologues of the spiracle associated in the shark with the first
gill-slit. The external ear is developed by the coalescence of six
rounded tubercles appearing in the bars or branchial arches that surround
the first gill-slit. In the course of ages the remaining gill-bars
(branchial arches) were also modified for special uses.
In relation with the external ear of man are found rudimentary muscles
that are no longer useful and ordinarily are not under the control of
the will. These muscles are the exact counterparts of well developed
functional muscles found in great numbers of the lower animals. They are
present in man as vestigial structures, because he is descended from
animals in whom these muscles were well developed and functional.
The anatomy of man reveals so many additional vestigial structures
that we may look upon him as a museum of obsolete anatomies; he is
an old curiosity shop containing many discarded tools, many outgrown
and aborted organs. The lower animals as well as man contain so many
useless (vestigial) structures among their useful organs, and they are
so significant of a former state of things in which they were useful,
that anatomists are willing to stake the theory of evolution upon their
presence alone. Evolution explains a multitude of other facts about man
that are inexplicable on any other theory.
[Illustration: FIG. 19. Brain of Fish (Bluefish). A, dorsal view; B, side
view; of, olfactory lobe; cr, cerebrum; ol, optic lobes; cb, cerebellum;
m, medulla; th, thalami.]
In addition to pointing out the possible track along which man has
evolved from a primitive protozoan it would be interesting as well as
exceedingly instructive to trace the development of each structure and
organ in his body. But the subject is a vast one, and cannot be presented
here even in briefest outline. Yet it will be very valuable to trace the
unfolding of one organ, and that the highest, as a sample of what occurs
with every part of the body. I refer to the _development of the brain_.
THE DEVELOPMENT OF THE BRAIN IN PHYLOGENY AND ONTOGENY.
Fig. 19 represents the brain of an average bony fish. It consists of
six swellings in a line, one before the other. Beginning from the
end towards the spinal cord, they are designated as follows, viz.: a
single median lobe, the medulla (Metencephalon), m; then in front of
this is another single median lobe, the cerebellum (Epencephalon),
cb; then the optic lobes (Mesencephalon), right and left, ol; then
the thalami (Thalamencephalon), which are small and hidden from
view by the encroachment of the two adjacent segments; then the
cerebrum (Prosencephalon), cr; then, finally, the olfactory lobes
(Rhinencephalon), of. In this fish the largest of the segments are the
optic lobes, ol.
[Illustration: FIG. 20.—Brain of Reptile (Turtle). A, dorsal view; B,
side view; of, olfactory lobe; cr, cerebrum; th, thalami; ol, optic
lobes; cb, cerebellum; m, medulla.]
The reptile’s brain (Fig. 20) shows similar parts with the same serial
arrangement. The reptile is a higher creature, a more intelligent
animal, than the fish; and in consonance with this fact the cerebrum, cr,
is the larger and more dominant part of the brain instead of the optic
lobes, ol.
[Illustration: FIG. 21.—Brain of Marsupial (Opossum). A, side view; B,
dorsal view; of, olfactory lobes; cr, cerebrum; ol, optic lobes; cb,
cerebellum; m, medulla. Thalami concealed from view by the backwardly
extended cerebrum; also the optic lobes are partially covered by the
cerebrum.]
[Illustration: FIG. 22.—Brain of Lemur (Lemur nigrifrons). A, dorsal
view; B, side view; cr, cerebrum; cb, cerebellum; m, medulla.]
In the marsupial (Fig. 21), a more intelligent animal still, the
cerebrum, cr, has grown so large that it extends backwards and partially
covers the optic lobes. It is to be observed that in the marsupial the
cerebellum, cb (like the cerebrum, cr), has evolved to a higher phase. It
consists of a median lobe, cb, which is larger than the median cerebellum
of the lower creatures mentioned, and of two lateral lobes, one on either
side, which have been acquired in the course of evolution. The median
lobe, the homologue of the single, median cerebellum of lower animals,
is larger than the lateral ones. The cerebellum of the marsupial has its
surface increased by fissures, while that of the fish and reptile is
smooth. The fissured cerebellum is a higher evolution than the smooth
ones. In the groups of animals referred to so far the cerebrum is smooth
and the olfactory lobes are still in front, though much encroached upon
in the marsupial by the enlarging cerebrum. In those animals still
higher in the scale of life, such as the prosimiæ (Lemurs), the cerebrum
has reached yet larger proportions and complexity, and has grown still
farther backwards towards the medulla, so that it hides from view a
considerable portion of the cerebellum (Fig. 22); it has also grown
forward, thus concealing largely the olfactory lobes. The cerebrum is
no longer smooth, but has a number of simple fissures and convolutions
(the higher animals have numerous complex fissures and convolutions). The
lateral lobes of the cerebellum have increased relatively more than the
central lobe, and the whole organ has advanced in complexity of fissures.
In the higher simiæ (monkeys and apes) the cerebrum has grown so far
backwards as to almost completely cover the cerebellum and medulla,
and its convolutions have become much more numerous and complex. The
cerebellum has also grown greatly, and its lateral lobes are now larger
and more complex than the central lobe.
[Illustration: PLATE XII.—Brain of man: dorsal and side views. The
cerebrum has grown so far backwards and forwards as completely to hide
the other segments of the brain when looked at from the dorsal surface.
From Carus’s “The Soul of Man.” By courtesy of The Open Court Publishing
Company.]
Finally, in man (Plate XII), the whole brain has grown so enormously that
it is three times larger than the brain of the highest simian creature.
The cerebrum, especially, has increased enormously in size. It has grown
not only backwards (overlapping cerebellum), upwards, and downwards
on the sides, it has grown so far forwards as not only to cover the
olfactory lobes, but also to project far beyond them. The cerebellum has
also increased in size and complexity, especially the lateral lobes. The
ideal vertical section (Fig. 23) shows diagrammatically in one figure all
these stages in the evolution of the human brain through the geologic
ages.
[Illustration: FIG. 23.—Ideal, vertical and sagital section, representing
the ontogeny and phylogeny of the human brain. of, olfactory lobe; crf,
cerebrum of fish; ol, optic lobes of fish; cbf, cerebellum of fish; m,
medulla of fish; cbr, cerebellum of reptile; cbo, cerebellum of opossum;
cbl, cerebellum of lemur; cbm, cerebellum of man; cr, cerebrum. Cerebrum
convoluted in lemur; much more convoluted in man. Cerebellum convoluted
from opossum upwards; mm, medulla of man.
Modified from Le Conte.]
It is a very interesting and instructive fact that in the development of
the human brain from the fertilized ovum these same stages, which are
permanent conditions in the zoölogical (taxonomic) series, are passed
through by it as transient stages.
One of the earliest conditions of the human brain is that in which it
presents three swellings in a serial arrangement. They are known from
behind, forwards as hindbrain, midbrain, and forebrain. For our purposes
it is sufficiently accurate to say that the =fœtal brain=, in developing
from this early condition to a later and higher condition, differentiates
the hindbrain into the _medulla_ (Fig. 24, m) and the _cerebellum_
(cb); the midbrain becomes the _optic lobes_ (ol); and the forebrain
differentiates into the _thalami_ (th) and the _cerebrum_ (cr). A little
later the cerebrum buds forth the olfactory lobes (of), so that the human
brain will consist of six fundamental segments,—one behind the other.
This is the _fish stage_ in the growth of the human brain. (Compare Fig.
24 with Fig. 19.)
[Illustration: FIG. 24.—Diagrammatic representation of the brain of
a human fœtus of the third week. Representing the fish-phase in the
ontogeny of the human brain. Side view. cr, cerebrum; th, thalamus; ol,
optic lobes; cb, cerebellum; m, medulla. The olfactory lobes at this
stage are very small and are not shown.
FIG. 25.—Dorsal view of the brain of a human fœtus of about seven weeks.
Representing the reptilian phase in the ontogeny of the human brain. cr,
cerebrum; th, thalami; ol, optic lobes; cb, cerebellum; m, medulla.
FIG. 26.—Side view of the brain of a human fœtus of about three months.
Representing the marsupial phase in the ontogeny of the human brain.
cr, cerebrum; ol, optic lobes; cb, cerebellum; m, medulla. The thalami
are completely, and the optic lobes partially, covered by the greatly
enlarged cerebrum.]
As development proceeds the most conspicuous growth of the brain is
observed in connection with the cerebrum and cerebellum. The cerebrum
particularly grows relatively and actually larger and larger, but does
not yet cover any portion of the optic lobes. This is the _reptile
stage_, represented in Fig. 25. The cerebrum, continuing to grow, finally
covers the front portion of the optic lobes. This is the _marsupial
stage_, and is shown in Figs. 26 and 27. Growing further, it soon covers
a greater or less portion of the cerebellum. These are the prosimian
(Lemur) and simian stages. Finally it grows so far backward as to
completely cover the cerebellum, and so far forward as to project much
beyond the olfactory lobes. This is the human stage (Plate XII).
[Illustration: FIG. 27.—Dorsal view of the brain (and spinal cord) of a
human fœtus of about three months. Representing the marsupial phase of
development. cr, cerebrum; ol, optic lobes; cb, cerebellum; m, medulla;
bs, brachial enlargement of the spinal cord; ls, lumbar enlargement. The
thalami are entirely covered and hidden from view by the cerebrum.]
In the study of the phylogeny of the brain we found that the cerebrum
in fish, reptile, and lower marsupial is smooth. In the primitive
primates (Lemuroidea) it is convoluted; in the simiidæ it is still more
convoluted, while in man it reaches the climax of complexity in the
size, number, and sinuosity of its convolutions. The object of these
convolutions is to increase the surface of the cortex of the brain,
the cortex being the seat of psychic phenomena. Other things being
equal, the greater the amount of cortex the greater is the intelligence.
During its embryonic development the human cerebrum passes also through
the stage of smoothness to a convoluted condition; then through stages
of increasing complexity of convolutions. Simultaneously with this
advance of cerebral organization, there is an unfolding of increasing
intelligence.
The cerebellum presides over the co-ordination of the muscular movements
of the body. It also, like the cerebrum, passes through the fish,
reptile, marsupial, lemur, and simian phases. At first it consists only
of the median lobe; then the lateral lobes appear, at first small in
size, but getting larger and larger until they greatly surpass in bulk
the more primitive median portion. At first the cerebellum is smooth,
but as it develops, its fissures become greater and greater, thus
increasing its cortex, which presides over the muscular movements. With
the developing cerebellum are associated increasing powers of muscular
co-ordination; increasing delicacy and complexity of muscular movements.
Thus the ontogeny of the brain recapitulates its phylogeny.
THE BRAIN AND PSYCHIC PHENOMENA.
The bearing of the theory of evolution on ideas of creation, design, and
kindred subjects may briefly be referred to in connection with our views
about the relation of psychic phenomena to the brain.
The study of the human brain in its anatomical, physiological and
psychological aspects has brought great thinkers, in all ages, into
the presence of phenomena that still baffle some of the most subtle
philosophers. Here we meet with such realities as self-consciousness,
perception, intellection and volition. Are these material entities of
such character that we may say they are exclusively products of the
activity of the brain, as the secretion of bile is the product of the
activity of the liver, as Cabanis taught? To us it seems clear that
such is not the case. One cannot take the specific gravity of love or
hate, of fear or joy, as one can that of bile; one cannot find a single
physical characteristic in any psychic phenomenon. The most physical of
all mental processes, viz., perception, has its psychological as well
as its physiological phases. The instreaming, through the senses, of
impressions from the external world, may be traced by the physiologist
along the different nerves of the body to the cortex cells of the brain.
All the phenomena that occur at and between these cortex cells and the
peripheral endings of the nerves may be formulated in terms of molecular
physics. But not so with that consciousness of these impressions which
we call perception. In the light of the present knowledge that we
possess, it seems to us that the only induction which the physiologist is
warranted in making is that, associated with molecular movements in the
brain is the phenomenon of perception. This leaves the field clear for
each thinker to speculate about the subject in such manner as seems to
him most rational. And the history of philosophy shows that many thinkers
have formulated theories upon the subject that range in character from
the materialism of Büchner to the idealism of Berkeley.
The view which teaches that psychic phenomena are correlated with
the physiological phenomena of the brain; that these phenomena have
undergone parallel[17] evolution, and “are as inseparable as are the
two sides of a sheet of paper” (Dr. Carus), appeals to us as the most
comprehensible one and at the same time the one most in consonance with
the known phenomena. We accept the view, then, that there is a mind
immanent in the brain.[18] The mind is conscious of its personality;
conscious of the external world through the innumerable perceptions
which reach it through the nervous system; conscious of its power to
build its percepts into concepts, and to reason about them; conscious
of its power of choice and of causing motion; and conscious of itself,
therefore, as a cause in producing effects; and, finally, it is conscious
of its power to adapt means to an end,—in short, it knows that it has the
power to design.
These facts are at the bottom of much of the philosophy of the present
and the past. The untutored savage, knowing that his personality can
cause motion, and beholding moving objects in nature, instinctively made
the induction that all these objects had personalities behind them. He
saw a spirit in his own voice that came back to him as an echo from
the rocks; he saw a personality in his shadow; he saw personalities in
falling stones, in running brooks, in waving foliage; he beheld them in
the raging tempest, in the thunder and the lightning, as well as in the
blazing sun and the twinkling stars; he saw spirits in the dead that came
back to him in dreams. In short, he recognized a separate personality
in every isolated phenomenon in nature. The child talking to its doll,
petting it, rebuking it, or whipping it; Xerxes castigating the ocean
for wrecking his ships, are illustrations of the strong human tendency
to project (or eject)[19] personalities into the inanimate objects of
nature. This natural, but lowly, phase of culture and philosophy is known
as _Fetichism_.
As encephalic and psychic evolution advanced; as men, with wider
knowledge and broadening experience, ascertained the laws that govern
the isolated phenomena of nature, the separate beings in every distinct
object and occurrence vanished from thought; but they still beheld a
separate personality in every great department of nature. The Romans,
for instance, saw Neptune as God of the Ocean, Pluto as God of the lower
world, Jupiter as God of the Heavens, and so on. This phase of culture
and philosophy, and therefore of religion, is _Polytheism_.
In the two phases of culture now briefly outlined the personalities
were grossly anthropomorphic. They were like human beings, capricious,
revengeful, subject to flattery, good and evil, and were therefore to be
placated and cajoled by sacrifices and offerings.
Psychic evolution continuing, there appeared from time to time great
thinkers who saw one “Infinite Personality” behind the cosmos.[20]
This “personality” is still in every phenomenon, though no longer as a
separate soul, but only as the separate manifestation of the Soul of
the Universe. This is _Monotheism_, a phase of culture which marks the
culmination of philosophy and religion through psychic evolution.
Our knowledge of the universe can be only a shadowy symbol of the
reality. The poverty of language is so great and the power of thought so
limited that the most subtle philosopher can form only an empty symbol
of the cosmic soul. The most ethereal symbols of the greatest thinkers
are necessarily incomplete in detail and anthropomorphic, in order to be
intelligible. The history of philosophy and religion shows that with the
evolution of mind and the acquisition of knowledge, the anthropomorphic
ideas of the soul of the cosmos become less crudely coarse and vulgar,
until the most elevated and refined ideas of monotheism are reached. But
even these refined ideas about the soul of the universe are necessarily
anthropomorphic, though in a vastly less degree than in the lower phases
of culture. One’s conceptions of this all-pervading soul immanent in the
universe are therefore profoundly modified by one’s kind and degree of
culture. In the words of Professor Fiske, the great scholar and subtle
thinker who has delved in the deepest mines of philosophy and come forth
weary and heavy-laden with their boasted treasures, has framed a very
different conception of God from that entertained by the priest at the
confessional.
A study of the human brain, then, and the soul resident therein prepares
us to believe that the cosmos has a soul (God) immanent in it. We can
readily grasp the idea that the soul of the cosmos may be self-conscious,
wills, thinks, acts, and designs.
This cosmic soul has been and is active in creation. In a low phase of
culture every distinct object of nature is looked upon as a separate
creation—a manufacture. With the progress of science the conception of
separate creative acts becomes greatly modified. The creative acts are
judged to be fewer in number and nobler in character. Finally, that phase
of highest culture which recognizes the law of universal evolution,
formulates the view of one continuous creative act, in which every
object is still a creation but not a separate creation,—only a separate
manifestation of one eternal act of creative energy. The history of
creation, which means the same thing as the history of evolution, shows
innumerable adaptations which may surely be considered as the work of
a cosmos designer. Evolution has profoundly modified our conceptions
of design in nature as it has those of creation. Every separate work
of nature, presents a separate, distinct and man-like design to the
uncultured. But, with advancing science, all these separate and petty
designs are swallowed up into fewer and grander designs, until at last,
through evolution, we reach the magnificent and ennobling conception of
one infinite and all-embracing design, persisting through infinite time
and extending throughout infinite space, which embraces every apparently
separate design.
Thus, while evolution destroys low anthropomorphic notions of the mode
of working of the Designer and simplifies while it purifies and vastly
ennobles our conceptions of this Designer, it yet replaces as much
teleology as it destroys. But the highest conceptions that the subtlest
philosophers are able to form of a cosmic Designer are necessarily
anthropomorphic in some degree, for they can only think in man-like ways.
We have seen in earlier pages of this book how, throughout the
incalculable ages of geologic time, innumerable living forms have
come upon the stage at different epochs, the forms of one epoch being
transmutations from those of an earlier one, and so on, back to the
beginning of life. The theory of universal evolution teaches that in
the abysmal depths of still earlier æons there was a time when no life
existed on the globe, for the globe was then a whirling ball of intensely
hot vapor; still further back there was a time when this ball of vapor
had not yet been born from that giant nebula—the primitive sun. Through
all the sweep of infinite time we see the multitudinous objects of
nature coming into existence, one after another, from primeval vapor,
and in accordance with laws the character and scope of which we begin to
partially understand. It is after the recounting of such well-known facts
as these that Professor Fiske makes the statement that Paley’s simile of
the watch is no longer applicable to such a world as ours. It must be
replaced, he says, by the simile of the flower; for the universe is not a
machine, but an organism with an indwelling principle of life; the world
was not made offhand, it has grown from more primitive conditions.
In studying the Diagram of Development (Fig. 18) it will be observed that
man is the highest and greatest fruitage of the tree of animal life. He
is the highest animal in the taxonomic series, as he is in the phylogenic
series. He has been the goal, and is the completion of organic evolution.
As Dana says, “there is a prophecy of man which runs through the whole of
geologic history, which was uttered by the winds and waves at their work
over the sands, by the rocks in each movement of the earth’s crust, and
by every living thing in the long succession, until man appeared to make
the mysterious announcements intelligible.”
The vital path from primitive protozoan to man has been a straight
and narrow one, and innumerable groups of animals have branched off
laterally. In so doing they departed forever from the man-ward path, and
developed obliquely along the diverging roads and bypaths of lower life
organizations. They may diverge still farther from the original parting
point, but can never get back into the man-ward road. They have lost the
golden opportunity and can never regain it.
Man is not only the highest creature that has ever appeared on the globe,
but it seems a safe induction to say that he is also the highest animal
that evolution will ever develop here.[21] Evolution, through Natural
Selection and other agencies, having spent most of its force in creating
the innumerable species of animals and plants that have lived in the past
and that are now living on the globe to-day, and having had as its goal
the creation of that highest and noblest of all creatures—man—is now
concentrating its force in further evolving man. Anatomists have reasons
to believe that man is now evolving, in many portions of his body, as
rapidly as did the horse through Tertiary Ages. Evolution is pushing him
on to higher and higher planes, along the straight and perpendicular
man-ward track that he has traveled from his protozoan ancestors; while
his simian relatives are diverging obliquely more and more from the
man-ward track. Through Natural Selection and _rational selection_
evolution seems now to be spending its main force especially on one
particular part of man’s body, viz.: his brain and its immanent mind.
The brain of a living, highly civilized man is larger than the brains
of men of the tenth century; the brains of these latter are larger than
those of palæolithic men. Evolution, having raised the body of man to
nearly its highest possible level, is now perfecting more and more his
brain, and therefore his thinking power, or, better, his mind. Through
his intelligence he is eliminating more and more the noxious plants and
dangerous animals that surround him, and is preserving and improving
those that are useful to him, and thereby making the organic world more
and more subservient to his purposes. He is even getting larger and
larger control over the mechanical, physical, and chemical forces of
nature, and the possibilities of his improvement in these directions are
almost boundless. Evolution for man now means psychic evolution, social
evolution; in short, civilization.
From what has been said it can readily be perceived that man,
zoölogically and psychologically, is by far the most important creature
on the globe. He seems to be the goal towards which evolution has
been steadily advancing throughout the geologic ages. It is for these
reasons that we believe no higher animal than man will be evolved on
the earth. Man himself will continue to evolve higher and higher. Well
may we say, with Sir William Hamilton, that there is nothing great
in the world but _man_, and nothing great in man but _mind_. Is it
a shallow philosophy which teaches that it was through design that
this most important creature was evolved as the topmost flower on the
highest and straightest branch of the tree of life? We do not think so.
One of the most profoundly interesting facts to be observed in that
higher evolution—psychic evolution—which is now mostly molding man,
is the fact of rational selection supplementing and largely replacing
Natural Selection. With the creation of man, _choice_ or will comes in
as a factor of ever-increasing importance. The active will to _use_
certain capacities and _disuse_ others will play a part in the further
development of man of ever-increasing importance and widening influence.
Use and disuse have been factors of commanding importance in modifying
the bodies and minds of the animal forms that led up to man. Use and
disuse will be factors of commanding influence in profoundly modifying
the brain, and therefore the mental constitution of man as he advances
in social evolution. The use of the brain along chosen lines will, on
well-known physiological principles, increase its organization and
therefore its power for manifesting psychic phenomena. These two factors
will continue to act and react in the future as they have in the past,
increased psychical activity enlarging the brain, and the more highly
organized brain augmenting the psychic phenomena. What is true of the
mind in general is also true of its varied manifestations. The history of
psychic evolution gives reason to believe that not only will the capacity
for thought be augmented and the power of the will increased in future,
but also the strength of selfishness will still further be weakened by
disuse and the power of sympathy augmented by practice. As our half-human
ancestors were evolving man-ward, and Natural Selection was augmenting
their brains, thus increasing their capacity for thought and, therefore,
their capacities for more varied experiences through life, there was a
concomitant increase in the period of infancy. The activities of the
lower animals are mostly of a simple character. They are for the purpose
of securing food, escaping enemies, and reproducing their kind. These
activities are comparatively so simple and have been repeated so often,
generation after generation for ages, that they have become thoroughly
organized, by heredity, in the offspring before they are born. When the
offspring are born they seek their food, they endeavor to avoid enemies,
and in due time procreate their kind without any teaching. With them
heredity is almost everything, and experience exceedingly small. These
facts can well be exemplified in studying the young of such animals
as fishes, amphibians, and reptiles. In the higher birds and mammals
Natural Selection has so augmented the size of the brain that their
psychic capacities are greatly increased. This increased intelligence is
accompanied with an augmented variety and complication of experiences.
The acts performed by animals now become so complex, numerous, and varied
that they are repeated with much less frequency than are the acts of
animals lower in the scale. Consequently, heredity has not had sufficient
time to so mold them into the germ-cells that they unfold as perfect
reflex or instinctive acts at birth. The hereditary units that carry
these acquired experiences of the parents in the developing embryo lie
dormant for a while and unfold slowly under the teaching and protection
of the parents for a varying period known as infancy. As Natural
Selection still further evolved the brains of our advancing half-human
ancestors, thus increasing their intelligence and making their lives
more replete with complex and varied experiences, there was a concomitant
prolongation of the period of infancy—the period of helplessness and
dependency. During this evolution of infancy Natural Selection compelled
the parents, especially the mother, to possess feelings other than those
of utter selfishness. They had to give thought not only to themselves but
also to the helpless creatures they brought into the world. The offspring
increasing in numbers, all associated together in varying degrees of
helpless infancy and dependent upon the care and protection of common
parents, the relationships of mother and father, brother and sister, must
by degrees have become more and more intimate as evolution proceeded,
until finally that social unit appears—the family. In the family personal
selfishness can no longer be the exclusively dominant motive to action.
Rudimentary sympathies appear. The individuals must conduct themselves so
as not to jeopardize the interests of the family. Thus other interests
than those of a purely personal character must influence their actions.
And thus, finally, the adumbrations of right and wrong conduct appear,
and we now find in the newly-created human species the germs of morality
and conscience. As social evolution proceeded, the self-regarding
faculties were more and more curtailed, and the other-regarding
sentiments were extended with ever-enlarging amplitude. Sympathy and
helpfulness for others were broadened more and more, including first the
clan, then the tribe, then the nation, and, finally, groups of the latter
were welded into empires. And the writing on the wall seems to indicate
the future federation of all the nations.
Among primeval men, who obtained their food by hunting out such edible
objects as were already in existence, war was universal. The supply of
fruit, fish, and game being strictly limited, men were compelled to
fight under penalty of starvation. As intelligence advanced and men
learned to cultivate useful plants and to domesticate animals, and as
they learned further to exchange by barter the products of their labor,
a much greater population could live upon a given area. These tribes
would be more powerful than their neighbors who still lived by hunting,
fishing, and such like, and would flourish at their expense. Through
agriculture and commerce men slowly learned that one man’s interest was
not necessarily opposed to another’s; they also learned, though it may be
ever so feebly, that fighting and plundering one another hindered rather
than promoted their welfare. Thus man slowly evolved from a primitive,
predatory civilization, in which war was universal and chronic, to the
higher industrial civilization, in which war is much less frequent and
less universal. Out of this primitive industrial civilization, which
has grown more and more complex with the passing years, have come the
arts and sciences, which give such added interest and value to modern
life. This evolving industrial civilization, by furnishing a wider
basis for political union through community of interest instead of mere
blood-relationship, has greatly extended the field over which moral
obligations are recognized as binding.[22] Social evolution is tending
to eradicate more and more, through disuse, the brutish instincts of
man; weakening his fighting propensities, his cruelty, his selfishness,
his passions; and strengthening, by use, his sympathies, his kindness,
his mercy, his sense of justice and honor, and his charity. The goal of
social evolution seems to be _men of character_,—men with the widest
possible knowledge of the laws of nature, physical, intellectual, and
moral; and with the desire and will to rightly obey these laws. Such
men will be both loving and lovable characters. In view of this may we
not supplement Sir William Hamilton’s aphorism, and say that there is
nothing great in mind but character? Since evolution is producing such
characters, though it may be seemingly ever so slowly, is it again a
shallow philosophy which teaches that there is a designer unfolding these
characters? We do not think so. And if there is a designer who has been
making towards this goal throughout the infinite sweep of bygone ages,
do we not have at least some faint adumbration of knowledge as to the
character of this designer? It seems to us that we do. Well may we say,
with Matthew Arnold, that there is immanent in the cosmos an eternal
soul, not ourselves, that makes for righteousness. This double assertion,
that there is a soul in the universe outside of ourselves, and that this
soul makes for right conduct, is the basis of fundamental importance in
all religions. There are many religions in the world, and many creeds
of the one great religion of christendom. They differ in many of the
transcendental doctrines that they teach, and in many of the rules of
conduct that they prescribe for their adherents; but they all contain as
their most fundamental and vitally important basis the double assertion
that there is a soul of the universe, and that this soul makes for
right conduct. The assertion may be thickly overlaid with superstitions
and petty rites by the untrained and dull intelligence of low races,
as in the Eskimos; or it may attain a high degree of development and
perfection, as among the Jews. The refinement and beauty of the double
conception are more and more enhanced with social evolution. Just
in proportion as civilization advances, and men come to reason more
carefully and entertain wider views of life, just to that extent do they
come to value more highly the essential truths of religion, while they
attach less and less importance to many superficial details. It is of
vastly greater moment to us that there is a cosmic soul in the universe
that makes for righteousness than that this soul is threefold or onefold
in its transcendental nature. Also of vastly more moment to us is a
belief in this soul than any opinions we may entertain about eating meat
on Friday or listening to attractive music on Sunday. A thoughtful mind,
penetrated with the conviction of the truth of evolution, entertains
views on all subjects pertaining to man, very different from those held
by one not familiar with the great theory. His conceptions of the first
Adam are profoundly modified by a flood of facts. If this flood sweep
him on irresistibly, and equally profoundly modifies his conceptions of
the second Adam, can it not be seen that even this is a fact of small
significance compared with that other fact of overwhelming importance,
viz.: the fact of the existence in the universe of a cosmic soul that
makes for righteousness? Man is essentially a religious animal, and
there is a very substantial philosophical basis for his religion.[23]
His religion may be highly colored with emotion, or it may be coldly
philosophical. When Herbert Spencer speaks of the eternal Power in the
universe which makes for righteousness and is manifested in every event
of the universe as the Unknowable, does he not do what Holy Writ has
already done? “Canst thou find out the Almighty unto perfection?” When
Carlyle speaks of the Universe as in very truth the star-domed city of
God, and reminds us that through every crystal and through every grass
blade, but most through every living soul, the glory of a present God
still beams, he means much the same thing that Mr. Spencer does when
he speaks of a Power that is inscrutable in itself, yet is revealed
from moment to moment in every throb of the mighty rhythmic life of
the universe. The only difference is that Mr. Spencer speaks in the
colorless, precise, and formal language of science, while Carlyle’s
language is colored by emotion; is, in fact, poetical.[24]
EVOLUTION AND SOCIAL PROBLEMS.
The relation of evolution to many social problems of vital importance
is a fascinating as well as very extensive subject. We have only space
to say that in order to understand the normal actions, as well as the
abnormal ones, of the members of society, and in order, therefore, to
understand and inaugurate rational methods of conducting education,
minimizing pauperism, vice, disease, and crime, it must constantly be
borne in mind that two great streams of tendencies have come down from
the ages in the germ cells—what we may call the diseased and animal
tendencies on the one hand, and the distinctively human and healthy
tendencies on the other.
The most characteristic of the human tendencies are abstract thought and
reflection, and therefore the power of choice or will, and altruism.
Also it must be borne in mind that environment is a force of commanding
influence. This environment (which the individual may make for himself
to a limited extent) may be propitious or adverse to the best human
and normal tendencies. The relative preponderance of the animal or the
human, the healthy, or the diseased tendencies, taken in conjunction with
the character of the environment, stamp man’s actions as normal (and
therefore right or wrong) or as abnormal, and therefore irresponsible.
Not to discriminate between such normal and abnormal persons is not in
accordance with either common morality or common sense. Neither is it
in accord with common sense, or morality, or humanity, for society to
deal with its habitual criminals and paupers, and subjects of hereditary
disease, in the utterly irrational manner that it does. When society
takes away from the criminal his personal liberty and places him in an
environment that theoretically reforms him and protects itself, why does
it not take cognizance of the fact that its theories are often woful
failures in practice? The criminal is often not reformed and he gets
into the category of habitual offenders; but society permits him, during
his intervals of freedom, to procreate his kind and send his polluted
cargoes of vicious heritages to helpless offspring. Is this humanity to
these offspring? It is the grossest inhumanity! Does society protect
itself by its intermittent detentions of habitual criminals? It probably
breeds three habitual criminals while it is failing in its efforts to
reform one. It is mostly by Nature’s prematurely killing off incorrigible
criminals by their diseases and intemperance, that these social pests
are kept within due bounds, and not through reformations accomplished in
improperly conducted prisons. It seems to us that every consideration of
justice and humanity cries aloud for the destruction of the procreating
glands in _habitual criminals_.[25] Castration should go hand in hand
with detention behind prison bars. Why should the habitual drunkard, for
instance, be permitted to evolve his poisoned germ cells into helpless
beings, giving them diseased bodies and vitiated moral characters, thus
foredooming them to life-long physical ailments and moral turpitude?
Removal of the procreating glands should be the penalty for chronic
alcoholism. In objection to this suggestion, some may prate of personal
liberty. What a multitude of outrages and brutalities the broad mantle of
personal liberty is often made to cover! In allowing personal liberty to
an undeserving individual, which more often means unbridled license to
that individual, a whole generation of offspring are frequently enslaved
by poverty, vice, crime, and disease in its manifold manifestations.
During organic evolution Natural Selection has been incessantly on the
watch for weaknesses of any kind, ruthlessly exterminating the helpless,
the weak, the sick, and those that in any way are unfit. In social
evolution Natural Selection has often been of necessity no less ruthless.
But during social evolution characters that are unfolding more and more
loving and lovable traits have so largely subordinated Natural Selection
as to permit the helpless, the old, the sick, and the unfit, to live,
thus strengthening those highest attributes of the greatest minds, viz.:
intelligent sympathy, pity and love.
But it seems to us that the highest altruism, in dealing kindly with an
abnormal, possible parent, will not continue long to stupidly overlook
the weighty rights of unborn children. Human selection of the socially
unfit will be dominated more and more, as social evolution unfolds
its fruits, by those minds that are advancing to the highest goals of
evolution, viz.: large minds of high character—widely informed minds, of
strong will and broad sympathies. And under these circumstances we may
hope that unborn generations will not be given over to total oblivion.
Well may we repeat, before concluding this little book, that man is not
only a creature of the present, but profoundly a product of the abysmal
ages of a bygone eternity. He is not only a composite chip of many old
human blocks, but of innumerable geologic ancestral blocks. He has in his
constitution simian, reptilian, piscine, and innumerable other chips,
so to speak, and is indeed of the earth earthy; for studies in heredity
not only illustrate the continuity of the human race, but also clearly
indicate the continuity of this race with more lowly animals. Man has
in his structure the indelible impress of the handiwork of these lowly
relatives. Upon him, as upon them, and upon all living creatures, the
forces of heredity and variation, of use and disuse, of environment and
Natural Selection, have been and are perpetually playing, evolving him in
one direction and innumerable creatures in other directions.
The goal of evolution seems to be men with Great Minds of High Character.
_There is nothing great in the world but man, nothing great in man but
mind, and nothing great in mind but character._
SECTION VII.
CLASSIFICATION OF ANIMALS AND PLANTS.
A SYNOPSIS OF THE ANIMAL KINGDOM.
In order that the reader may appreciate to some extent the relative
positions of the different groups of animals, extinct and living, in the
scale of life, the following brief classification may be useful. This
synopsis is especially intended to help readers who are not familiar
with elementary zoölogy to understand the significance of the different
types of animals found in the strata of different geologic periods, and
more particularly to grasp the meaning of the Diagram of Development. The
animals are usually mentioned in the order of their position in the scale
of life, commencing with the lowest and simplest.
SYNOPSIS OF GROUPS.
A. PROTOZOA. Unicellular animals, dissociated, or associated in simple,
loose colonies of similar organisms. Many have an exoskeleton of lime,
flint, or other material. Reproduction by fission and by temporary or
permanent conjugation.
B. METAZOA. Multicellular animals, consisting of a large number of cells
associated together to form single, complex individuals. The cells of
an individual are usually differentiated into several kinds performing
special functions. Reproduction in the higher forms is sexual; in the
lower forms it is often by budding as well as sexual.
SYNOPSIS OF THE BRANCHES OF ANIMALS.
GROUP A. PROTOZOA.
Branch I.—=Protozoa.= Characteristics already defined.
Class 1.—_Monera._
Class 2.—_Rhizopoda_: Amœba, Arcella, Foraminifera, Difflugia, Quadrula.
Class 3.—_Gregarinida_: Gregarina.
Class 4.—_Infusoria_: Noctiluca, Paramecium, Stylonychia.
GROUP B. METAZOA.
Branch II.—=Porifera.= Sponges are animals with their cells arranged in
two well-defined layers, one of which is internal (endoderm) and the
other external (ectoderm). There is a middle stratum of cells (mesoglœa)
which does not attain to the definiteness of a mesoderm. Sponges do not
possess a body cavity (cœlome); they possess, essentially, a bilateral
symmetry. The body varies greatly in shape, and is traversed by canals
having large openings (oscula) and numerous small openings (pores) on
the surface. The ectoderm is continued through the pores into afferent
canals; the endoderm cells line most of the internal (efferent) cavities,
and are mostly flagellate; the mesoglœa contains a skeleton of flint,
lime, or spongin. Reproduction may be by budding or sexual (either
hermaphroditic or unisexual).
Branch III.—=Cœlenterata.= Animals possessing radial symmetry. There
is no body cavity (cœlome), but there is a primitive digestive cavity
(enteron). The body consists of two layers, an ectoderm and endoderm;
between these two layers there is a mesoglœa of jelly-like consistency;
in the simplest cases there are no cells in the mesoglœa, but secondarily
endodermal cells may migrate into it. Stinging cells are generally
present.
There are two divergent types of structure. The more primitive one is the
sessile tubular hydroid, which may be compared to a gastrula furnished at
one end with a crown of tentacles surrounding the opening of the enteron,
and fixed at the opposite end. The less primitive, derived form, is the
active jellyfish (medusoid) type. The hydroid type often constructs a
calcareous skeleton known as coral. One life history may present both
types (alternation of generations). Reproduction is sexual or by budding,
in the latter case often resulting in the formation of colonies.
Class 1.—_Hydrozoa_: Hydra, Jellyfish.
Class 2.—_Actinozoa_: Sea-Anemones, Coral Polyps.
Class 3.—_Ctenophora_: Comb-Bearers.
Branch IV.—=Echinodermata.= Animals, the larvæ of which possess bilateral
symmetry, while the adults have radial symmetry. Even the adults exhibit
to a varying extent a tendency to bilateral symmetry. Lime is always
deposited in the mesodermic substance (mesenchyme). From the primitive
digestive canals of the larvæ pouches grow out to form the usually
spacious body cavity and the characteristic water vascular system. The
latter and the nervous system exhibit generally a typical five-rayed
arrangement. During development there is a distinction between mesoblast
derived from gut pouches and mesenchyme produced from migrated amœboid
cells. Complicated metamorphosis.
Class 1.—_Cystoidea._
Class 2.—_Blastoidea._
Class 3.—_Crinoidea_: Stone-lily.
Class 4.—_Asteroidea_: Star-fishes.
Class 5.—_Echinoidea_: Sea-urchins.
Class 6.—_Holothuroidea_: Sea-cucumbers.
Branch V.—=Vermes.= The term “worms” includes a “heterogeneous mob,” a
collection of classes whose relationships are poorly understood. But
they are of great zoölogical interest, for, amid the diversity, there
can be discerned affinities with Cœlenterata, Echinodermata, Arthropoda,
Mollusca, and Vertebrata. They possess a well-defined mesoderm. They
possess bilateral symmetry and have, as a rule, a head, tail, dorsal
and ventral surfaces, and right and left sides. The lower worms are
unsegmented. In the higher ones the digestive tract extends from the
head to the end of the body; a dorsal vessel is usually present above
the digestive tract; the nervous system consists of a supra-œsophageal
ganglion (brain) and a simple or more commonly double, ventral,
ganglionated cord; there is a body cavity (cœlome) lined with mesoderm;
true jointed appendages are never present.
Class 1.—_Platyhelminthes_: Flat-worms.
Class 2.—_Nemathelminthes_: Round-worms.
Class 3.—_Rotatoria_: Rotifer.
Class 4.—_Bryozoa._
Class 5.—_Brachiopoda_: Lampshells.
Class 6.—_Nemertina._
Class 7.—_Enteropneusta_: Balanoglossus.
Class 8.—_Gephyrea_: Star-worms.
Class 9.—_Annulata_: Earth-worms, Leeches, Sea-worms.
Branch VI.—=Arthropoda.= Animals with bilateral symmetry. Bodies
segmented, but not uniformly so. Several or all of the segments bear
paired jointed appendages variously modified. Chitinous exoskeleton.
Digestive canal beneath the heart. Supra-œsophagel ganglion (“brain”)
connected by a nerve ring round the gullet with a double chain of ventral
ganglia. Cœlome small in the adult. Sexes almost always separate. Often
some metamorphosis.
Class 1.—_Crustacea_: Trilobites, Shrimps, Crabs.
Class 2.—_Arachnida_: Spider, Scorpion.
Class 3.—_Onychophora_: Peripatus.
Class 4.—_Myriapoda_: Centipede.
Class 5.—_Insecta_: Cockroach, Ants, Butterfly.
Branch VII.—=Mollusca.= Unsegmented animals, possessing, fundamentally,
a bilateral symmetry. A very characteristic structure is the “foot”—a
muscular protrusion of the ventral surface. Typically, a projecting fold
from the dorsal surface of the body forms a mantle, or pallium; the
mantle often secretes a single or double shell covering the viscera.
The mantle and shell may both be absent. The central nervous system
consists of paired ganglia with connecting commissures, viz.: cerebral,
pleural, pedal, and visceral ganglia. Heart possesses two auricles and
one ventricle. Respiration generally by gills. Frequently there are two
larval stages. Development is often direct.
Class 1.—_Lamellibranchiata_: Clam, Oyster.
Class 2.—_Scaphopoda._
Class 3.—_Gasteropoda_: Snail, Whelks, Slugs.
Class 4.—_Amphineura_: Chitons.
Class 5.—_Cephalopoda_: Squids and Cuttlefish.
Branch VIII.—=Vertebrata or Chordata.= Vertebrates are animals having a
distinct body cavity (cœlome) and a segmental arrangement of parts. A
hypoblastic skeletal notochord is always present in the embryo, but tends
to be replaced by an axial skeleton of mesoblastic origin (backbone).
Gill slits are always present in the embryo and may or may not persist in
adult life. Gill-lamellæ do not occur above Amphibians. Heart is ventral.
Central nervous system is dorsal. Eye begins to develop as an outgrowth
from the brain.
Class 1.—_Tunicata._
Class 2.—_Leptocardii._
Class 3.—_Marsipobranchii._
Class 4.—_Pisces._
Class 5.—_Amphibia._
Class 6.—_Reptilia._
Class 7.—_Aves._
Class 8.—_Mammalia._
Class 1.—_Tunicata._ The tunicates are remarkable animals, and seem
to stumble on the border line between Invertebrates and Vertebrates.
Their vertebrate characteristics—gill slits, notochord, dorsal nervous
system, and brain eye—are generally discernible only in the free-swimming
larval state. They generally degenerate as they progress towards the
adult condition, and diverge greatly from the vertebrate type. They are
mostly stationary. They are multicellular animals possessing bilateral
symmetry. The body is enveloped by a thickened cuticle containing
cellulose. The pharynx, perforated with the gill slits, is surrounded by
a peribranchial chamber (atrium) which communicates with the exterior
by an atrial opening. Heart is simple and tubular. The nervous system
is generally reduced to a single ganglion. Nephridia are absent.
Hermaphrodites. Usually a metamorphosis.
Class 2.—_Leptocardii._ Simple, worm-like vertebrate animals represented
by a single distinct type—amphioxus or lancelet. The central nervous
system consists of a spinal cord, and a very ill-defined, rudimentary
brain. No skeleton other than an unsegmented and persistent notochord
which projects beyond the anterior end of the nerve cord. No scales. Gill
slits are very numerous in the adult. Amphioxus is widely removed from
the fishes by the absence of skull, jaws, definite brain, sympathetic
nervous system, ear, eye, genital ducts, spleen, and definite heart, the
latter being simple and tubular. No pectoral or pelvic limbs (fins).
Blood colorless; gastrula ciliated and free-swimming. Metamorphosis.
Class 3.—_Marsipobranchii._ Worm-like vertebrates having round mouths
without distinctly developed jaws; no jaw-bones. Without scales and
without paired limbs (fins). Six or seven gill pouches. Skeleton consists
of persistent, unconstricted, cartilaginous notochord. No sympathetic
nervous system. Single nasal sac. No conus arteriosus, no spleen or
pancreas. Undivided segmental duct.
Class 4.—_Pisces._[26] Aquatic, cold-blooded vertebrates, with a movable
lower jaw. Cartilaginous or osseous skeleton, with paired pectoral and
pelvic fins, supported by fin rays (_radials_ diverging from several
_basal_ pieces); also unpaired fins. No sternum. Exoskeleton of bony
plates or scales. Skull has usually one occipital condyle. Breathing
by permanent gills attached to gristly or bony arches on the sides of
the gill clefts. In most fishes the digestive cavity gives origin to an
air bladder which may or may not remain permanently connected with the
digestive cavity. It mostly serves a hydrostatic purpose, but in some of
the more primitive fishes (Amia, Lepidosteus) it is occasionally of some
slight use in respiration. Heart consists of single auricle and single
ventricle, and contains only venous blood; there is a sinus venosus and
often a conus arteriosus. No inferior vena cava. No allantois. Most
fishes lay eggs which are fertilized in the water.
Sub-class 1.—_Elasmobranchii._
Order 1.—_Plagiostomi_: Sharks, Rays.
Order 2.—_Holocephali_: Chimæroids.
Sub-class 2.—_Teleostomi._
Order 1.—_Crossopterygii_: Polypterus, Calamoichthys.
Order 2.—_Ganoidei_: Sturgeon, Garpike, Amia, Polyodon.
Order 3.—_Dipnoi_: Lung-fishes, e. g., Ceratodus, Protopterus, and
Lepidosiren.
Order 4.—_Teleostei_: Perch, Cod, Salmon, Eel.
Class 5.—_Amphibia._ In the evolution of vertebrates the Amphibians
represent those forms which made the transition from aquatic to
terrestrial life, but have lingered near the water. Certain acquisitions
gained by the Dipnoi, such as a three-chambered heart and lungs, have
been accentuated and firmly established by the Amphibians.
Amphibia are cold-blooded vertebrates whose larval forms always have
gill arches bearing gills. In some forms the gills are retained
throughout life, though the adults always possess functional lungs.
Nasal sacs open posteriorly into the mouth. In existing forms there
is rarely any exoskeleton. There are two occipital condyles. Unpaired
fins are frequently present, though they possess no fin rays. When
limbs are present they possess distinct digits and conform to the same
type as those of the higher vertebrates. Heart has two auricles and
one ventricle. There is an inferior vena cava. The intestine ends in a
cloacal chamber, as do also the urinogenital ducts. Eggs almost always
laid in the water. Often a marked metamorphosis.
Order 1.—_Urodela._ Amphibia which retain the tail throughout life.
The order is subdivided into:
a. _Perennibranchiata_, which retain the gills throughout life:
_Siren_, _Proteus_.
b. _Caducibranchiata_; no persistent gills: _Triton_, _Salamandra_.
Order 2.—_Gymnophiona._ Body snake-like; no feet; young with gills:
_Cœcilia_.
Order 3.—_Stegocephala._ Extinct forms: _Archegosaurus_.
Order 4.—_Anura._ Tailless amphibia; body short, with four limbs;
larvæ tailed: _Frog_, _Toad_.
Class 6.—_Reptilia._ Cold-blooded, air-breathing vertebrates. Limbs
usually ending in claws; limbs sometimes absent; exoskeleton of
scales; ribs well developed; incomplete double circulation; heart is
four-chambered in the highest forms; oviparous; no metamorphosis; embryo
with an amnion and allantois.
The following are some of the orders that have become extinct, viz.:
a. _Theromorpha_: Mammal-like saurians.
b. _Ichthyosauria_: Swimming saurians.
c. _Pterosauria_: Flying saurians.
d. _Dinosauria_: Colossal land saurians capable of rising and resting
on the hind legs.
The following are the living orders, viz.: a, _Ophidia_; b, _Lacertilia_;
c, _Chelonia_; d, _Crocodilia_.
Class 7.—_Aves._ Feathered vertebrata; heart four-chambered;
warm-blooded; lungs with accessory air-sacs; bones dense and hollow;
jaws encased in horny beaks in modern forms; the fore-limbs form wings;
oviparous; eggs are very large and covered by calcareous shell.
Sub-class 1.—_Saururæ_: Archæopteryx.
Sub-class 2.—_Odontornithes_: Ichthyornis, Hesperornis.
Sub-class 3.—_Ratitæ_: Smooth sternum.
Sub-class 4.—_Carinatæ_: Keeled sternum.
Class 8.—_Mammalia._ Animals having the body covered with hair;
warm-blooded; young nourished with milk secreted from mammary glands;
lower jaw articulating directly with the skull, the quadrate becoming the
malleus (ear-bone); heart four-chambered and with the aorta reflected
over the left bronchus; red blood-corpuscles non-nucleated; complete
diaphragm; brain large, especially the cerebrum and cerebellum; uterine
gestation; viviparous.
Sub-class 1.—_Ornithodelphia_: Order Monotremes. Urinary and genital
canals opening into cloaca. Laying large eggs.
Sub-class 2.—_Didelphia_: Order Marsupials. Animals having pouch for
protection and growth of prematurely born embryos.
Sub-class 3.—_Monodelphia_: Placental Mammals.
Order 1.—_Edentata._
Order 2.—_Rodentia._
Order 3.—_Insectivora._
Order 4.—_Cheiroptera._
Order 5.—_Cetacea._
Order 6.—_Sirenia._
Order 7.—_Proboscidea._
Order 8.—_Hyracoidea._
Order 9.—_Ungulata._
Order 10.—_Carnivora._
Order 11.—_Primates._
_Primates_ are an order of Monodelphia or Placentalia, including lemurs,
monkeys, and man. They are nearly all adapted to an arboreal life. The
hand (manus) and the foot (pes) nearly always have five digits provided
with flat nails. The pectoral and pelvic limbs are prehensile, owing to
the fact that the thumb (pollex) and big toe (hallux) are more or less
completely opposable to the other digits. The orbital fossa is completely
surrounded by a bony rim. The femur does not have a third trochanter. The
internal condyle of the humerus does not have a foramen above it. The
clavicles are always well developed. The testes descend into a scrotum.
On the thoracic region there are nearly always two teats. The placenta
may be non-deciduate, or deciduate and metadiscoidal.
The order of Primates is subdivided into the following sub-orders, viz.:
Sub-order 1.—_Lemuroidea._
Sub-order 2.—_Anthropoidea._
_Lemuroidea._ The Lemurs are small, monkey-like quadrupeds. They are
mostly nocturnal, arboreal creatures of comparatively low organization.
The body is furry. The orbital and temporal fossæ freely communicate. The
lachrymal foramen is situated outside the orbital fossa. The dentition
of the Lemurs varies greatly; in some of them it is 2/2 1/1 3/3 3/3 for
both jaws. In nearly all of them the median incisors of the upper jaw are
separated by a median space. Both feet have flat nails on all the digits,
except the second of the hind-foot, which has a claw. The thumb (pollex)
and the big toe (hallux) are well developed. The cerebral hemispheres are
only slightly convoluted, and do not entirely overlap the cerebellum. The
transverse colon is almost always folded on itself. There may be a pair
of teats on the abdomen. The uterus is two-horned, and the placenta is
diffuse.
This sub-order comprises the Lemurs proper (_Tarsius_, _Lemur_, and other
genera) and the Aye-Ayes (_Chiromys_).
_Anthropoidea._ The Anthropoidea are the most highly organized Primates.
They are chiefly modified for an arboreal life. The body is hairy instead
of furry, but only slightly so in man. The incisors do not exceed 2/2;
the molars are 3/3, except in the marmosets, where they are 2/2. The
upper, median incisors are in close contact. The orbital and temporal
fossæ are separated by a broad vertical plate. The lachrymal foramen
is situated inside the orbital fossa. All of the digits are provided
with flat nails, except in the Hapalidæ, in which all except the big
toe (hallux) are provided with a claw. In some the thumb (pollex) is
rudimentary or absent. The clavicle is well developed. The cerebrum
is usually richly convoluted, and more or less completely covers the
cerebellum. The uterus has no horns. The placenta is deciduate and
metadiscoidal.
The Anthropoidea are subdivided into the two following groups:
Super-family 1.—_Platyrrhinæ_ (New-World Monkeys).
Super-family 2.—_Catarrhinæ_ (Old-World Monkeys).
The Platyrrhinæ or New-World Monkeys are subdivided into the following
families, viz.:
Family 1.—_Hapalidæ._
Family 2.—_Cebidæ._
The Catarrhinæ or Old-World Monkeys are subdivided into the following
families, viz.:
Family 1.—_Cercopithecidæ._
Family 2.—_Simiidæ._
Family 3.—_Hominidæ._
_Hapalidæ._ The Hapalidæ or Marmosets are no larger than squirrels, being
the smallest monkeys. They are found mostly in Brazil.
There is a broad septum between the nostrils. Their dentition is 2/2 1/1
3/3 2/2, and is distinctive, for the remaining Anthropoidea have 3/3
molars. The tail is long, hairy, and non-prehensile. The arms are not
longer than the legs. The thumb (pollex) is long, but is not opposable.
All the digits except the great toe (hallux), which is small, have
curved, pointed claws. There is no bony external auditory meatus. There
are no cheek pouches, or ischial callosities. The Hapalidæ often bear
three young ones at a birth, whereas the other Anthropoidea commonly bear
but one. There are two genera of Marmosets, viz.: _Midas_ and _Hapale_.
_Cebidæ._ The Cebidæ are most at home in Brazil. They have a broad
septum between the nostrils. Many of them have prehensile tails. The
dental formula is 2/2 1/1 3/3 3/3, and is characteristic. There is no
bony external auditory meatus. There are no cheek pouches, or ischial
callosities. All the digits are provided with flat nails. The thumb
(pollex) is not opposable.
This family includes the following genera, viz.: Tee Tees (_Callithrix_),
Howling Monkeys (_Mycetes_), Spider Monkeys (_Ateles_), Squirrel Monkeys
(_Chrysothrix_), and Capuchin Monkeys (_Cebus_).
_Cercopithecidæ._ This family includes the Old-World dog-like Apes. They
are quadrupeds, and the muzzle or snout is quite dog-like. There is a
narrow septum between the nostrils. The dental formula is 2/2 1/1 2/2
3/3. The sternum is narrow. The tail is not prehensile. The cæcum has no
appendix vermiformis. There is a bony external auditory meatus. There may
or may not be cheek pouches. Over the rough surface of the everted ischia
the skin forms callosities (ischial callosities) which are often brightly
colored. The thumb (pollex), when present, is opposable. This family
includes two genera, Macaques (_Macacus_) and Baboons (_Cynocephalus_).
_Simiidæ._ This family includes the Anthropoid Apes of the Old World.
They are less quadrupeds than the former, often walking in a semi-erect
position. The dental formula is 2/2 1/1 2/2 3/3. The sternum is broad.
The cæcum has an appendix vermiformis. The nasal septum is narrow. The
pectoral limbs are much longer than the pelvic ones. There is a bony
external auditory meatus. There are no cheek pouches. Only in the Gibbons
are there ischial callosities, in whom they are small. The thumb (pollex)
is opposable. No visible tail. This family includes the following genera,
viz.: Chimpanzees (_Anthropopithecus_), Gorillas (_Gorilla_), Orangs
(_Simia_), and the Gibbons (_Hylobates_).
_Hominidæ._ This family of Anthropoidea includes only the human species
(_Homo sapiens_). The dental formula is 2/2 1/1 2/2 3/3. The tail is
not visible. The Hominidæ differ from the Simiidæ, structurally, mainly
in the more perfect assumption of the erect attitude. There is a more
complete adaptation of the pelvic limbs to bearing the weight of the
body, correlated with compensating alteration in the curvature of the
spinal column. The big toe (hallux) is not opposable, and also it is
often longer, never shorter than the other toes, and is not abducted
from them. He has a far better heel than the Simiidæ. The thumb is far
more opposable in man. There is a greater length of the pelvic limbs
compared with the pectoral limbs. The canine teeth are much smaller and
do not project beyond the level of the others. The brain has a much
greater size and complexity. Man has a larger forehead, smaller cheek
bones, smaller supraorbital ridges, a less protrusive face, and a true,
well-marked chin.
The Simiidæ are subdivided into the two following groups, viz.:
Sub-family 1.—_Hylobatinæ._
Genus 1.—_Hylobates_ (Gibbons).
Sub-family 2.—_Simiinæ._
Genus 1.—_Simia_ (Orangs).
Genus 2.—_Gorilla_ (Gorillas).
Genus 3.—_Anthropopithecus_ (Chimpanzees).
SYNOPSIS OF THE PLANT KINGDOM.
GROUP A. PROTOPHYTA.
GROUP B. METAPHYTA.
The Metaphyta are subdivided into:
1. _Cryptogams_: Flowerless plants.
2. _Phanerogams_: Flowering plants.
The Cryptogams are subdivided into:
1. _Thallophyta_: Seaweeds, Fungi, Lichens.
2. _Bryophyta_: Mosses, Liverworts.
3. _Pteridophyta_: Ferns, Horsetails, Clubmosses.
The Phanerogams are subdivided into:
1. _Gymnospermæ_:
Order a.—_Cycadaceæ_: Cycads.
Order b.—_Coniferæ_: Pines, Spruces, Cypresses.
2. _Angiospermæ_:
Class 1.—_Monocotyledones_: Grasses, Palms.
Class 2.—_Dicotyledones_: Oaks, Poplars, Elms.
SECTION VIII.
WORKS OF REFERENCE.
WORKS OF REFERENCE.
The following books have been the constant companions of the author
during the preparation of his “First Book in Organic Evolution”:—
GRANT ALLEN, The Colours of Flowers.
A. C. ABBOT, Principles of Bacteriology.
FRANK BAKER, The Ascent of Man.
THOMAS BELT, Naturalist in Nicaragua.
H. W. BATES, Naturalist of the Amazons.
F. E. BEDDARD, Animal Coloration.
A. H. BRADFORD, Heredity and Christian Problems.
F. M. BALFOUR, A Treatise on Comparative Embryology.
D. G. BRINTON, Races and Peoples.
P. C. BURT, A History of Modern Philosophy.
PAUL CARUS, The Soul of Man.
PAUL CARUS, The Ethical Problem.
PAUL CARUS, The Idea of God.
PAUL CARUS, Homilies of Science.
PAUL CARUS, Fundamental Problems.
ARTHUR CLARKSON, A Text-Book of Histology.
EDWARD CLODD, The Story of Creation.
EDWARD CLODD, The Story of Primitive Man.
EDWARD CLODD, A Primer of Evolution.
CARPENTER-DALLINGER, The Microscope and its Revelations.
A. DE QUATREFAGES, The Natural History of Man.
E. D. COPE, The Primary Factors of Organic Evolution.
CHARLES DARWIN, The Origin of Species.
CHARLES DARWIN, The Descent of Man.
CHARLES DARWIN, Animals and Plants under Domestication.
J. D. DANA, New Text-Book of Geology.
BASHFORD DEAN, Fishes, Living and Fossil.
J. W. DRAPER, History of the Intellectual Development of Europe.
J. W. DRAPER, Conflict between Religion and Science.
H. H. DONALDSON, The Growth of the Brain.
R. L. DUGDALE, The Jukes.
HENRY DRUMMOND, The Ascent of Man.
HAVELOCK ELLIS, Man and Woman.
HAVELOCK ELLIS, The Criminal.
JOHN FISKE, The Unseen World.
JOHN FISKE, The Idea of God.
JOHN FISKE, The Destiny of Man.
JOHN FISKE, Excursions of an Evolutionist.
JOHN FISKE, Myths and Myth-Makers.
ENRICO FERRI, Criminal Sociology.
SIR W. H. FLOWER, Osteology of the Mammalia.
FUNK and WAGNALL, Standard Dictionary of the English Language.
THEODORE GILL, The Families of Fishes.
THEODORE GILL, Articles on Fishes in the Riverside Natural History.
JOHN C. GALTON, Ecker’s The Human Brain.
FRANCIS GALTON, Hereditary Genius.
FRANCIS GALTON, Natural Inheritance.
FRANCIS GALTON, English Men of Science, their Nature and Nurture.
C. GEGENBAUR, Elements of Comparative Anatomy.
J. M. GUYAU, Education and Heredity.
GEDDES and THOMSON, The Evolution of Sex.
HARPER’S Latin Dictionary.
T. H. HUXLEY, Anatomy of Vertebrated Animals.
T. H. HUXLEY, Man’s Place in Nature.
T. H. HUXLEY, Origin of Species.
T. H. HUXLEY and MARTIN, Practical Biology.
T. H. HUXLEY, Science and Culture, and other Essays.
HERTWIG-MARK, Text-Book of Embryology.
DAVID J. HILL, Genetic Philosophy.
HERTWIG-CAMPBELL, The Cell.
ROBERT HARTMAN, The Anthropoid Apes.
GEORGE HASLAM, Ecker’s Anatomy of the Frog.
REV. W. HOUGHTON, Sketches of British Insects.
E. KLEIN, Micro-organisms and Disease.
G. T. LADD, Outlines of Physiological Psychology.
CESARE LOMBROSO, The Man of Genius.
SIR JOHN LUBBOCK, The Beauties of Nature.
SIR JOHN LUBBOCK, Ants, Bees, and Wasps.
ARNOLD LANG, Text-Book of Comparative Anatomy.
JOSEPH LEIDY, Fresh-water Rhizopoda of North America.
LIDDELL and SCOTT, Greek-English Lexicon.
SIR CHARLES LYELL, Antiquity of Man.
SIR CHARLES LYELL, Principles of Geology.
JOSEPH LE CONTE, Evolution and its Relation to Religious Thought.
JOSEPH LE CONTE, Elements of Geology.
C. S. MINOT, Human Embryology.
ST. GEORGE MIVART, The Genesis of Species.
ST. GEORGE MIVART, Lessons in Elementary Anatomy.
ST. GEORGE MIVART, The Common Frog.
ST. GEORGE MIVART, The Cat.
A. M. MARSHALL, Vertebrate Embryology.
HENRY C. MCCOOK, American Spiders.
F. MAX MÜLLER, Anthropological Religion.
C. LLOYD MORGAN, Animal Life and Intelligence.
C. LLOYD MORGAN, Animal Biology.
O. T. MASON, Woman’s Share in Primitive Culture.
DANIEL OLIVER, Lessons in Elementary Botany.
RICHARD OWEN, Anatomy of Vertebrates.
A. S. PACKARD, Zoölogy.
PARKER and HASWELL, Text-Book of Zoölogy.
OSCAR PESCHEL, The Races of Man.
E. P. POULTON, The Colours of Animals.
J. W. POWELL, Truth and Error, or, The Science of Intellection.
TH. RIBOT, Heredity.
ERNEST RENAN, The Life of Jesus.
G. J. ROMANES, Darwin and After Darwin.
S. H. REYNOLDS, The Vertebrate Skeleton.
OSCAR SCHMIDT, The Mammalia.
OSCAR SCHMIDT, Descent and Darwinism.
SCHAFER and THANE, Quain’s Elements of Anatomy.
KARL SEMPER, Animal Life.
HERBERT SPENCER, Principles of Biology.
W. B. SCOTT, An Introduction to Geology.
N. S. SHALER, First Book in Geology.
J. B. SUTTON, Evolution and Disease.
R. S. TARR, Elementary Geology.
J. A. THOMSON, Outlines of Zoölogy.
E. B. TYLOR, Anthropology.
JAMES TYSON, The Cell Doctrine.
LESTER F. WARD, Dynamic Sociology.
LESTER F. WARD, Outlines of Sociology.
ALFRED WEBER, History of Philosophy.
A. D. WHITE, A History of the Warfare of Science with Theology.
A. WEISMANN, Essays upon Heredity.
A. WEISMANN, The Germ-Plasm.
A. R. WALLACE, The Malay Archipelago.
A. R. WALLACE, Darwinism.
E. B. WILSON, The Cell in Development and Inheritance.
R. WIEDERSHEIM, Comparative Anatomy of Vertebrates.
R. WIEDERSHEIM, The Structure of Man.
C. F. WINSLOW, Force and Nature.
WILLIAM WHEWELL, History of the Inductive Sciences.
B. G. WILDER, Anatomical Technology.
B. G. WILDER, Article “Brain,” Reference Handbook of the Medical
Sciences.
ERNST ZIEGLER, General Pathology.
SECTION IX.
GLOSSARY.
GLOSSARY.
=A-chro´ma-tin= [Gr. _a_-priv.; _chroma_, color.] The nuclear hyaloplasm.
=A-chro-ma-top´si-a= [Gr. _a_-priv.; _chroma_, color; _opsis_, sight.]
Color-blindness.
=Ac-ti-no-zo´a= [Gr. _aktis_, ray; _zoon_, animal.] A division of
Cœlenterates embracing the sea-anemones and coral-polyps.
=Al-lan´to-is= [Gr. _allas_, sausage; _eidos_, form.] A membranous,
sack-like appendage developed from the hinder part of the embryonic
alimentary tract and which serves the purpose of effecting oxygenation
and other changes in the blood in reptiles, birds, and mammals.
=Am-blyp´o-da= [Gr. _amblys_, blunt; _pous_, foot.] An extinct order of
ungulates having elephantine feet and whose navicular bone was supported
by the cuboid.
=Am-blys´to-ma= [Gr. _amblys_, blunt; _stoma_, mouth.] A genus of
amphibians remarkable for the transformations they undergo. When
undeveloped they represent the formerly recognized genus _Siredon_. Some
species are called _axolotls_.
=Am´i-a= [Gr. _amia_, a kind of tunny.]
=Am-i-to´sis= [Gr. _a_-priv.; _mitos_, thread.] Direct cell-division;
cell-division without the formation of nuclear figures.
=Am´mon-ites= [Egyptian _Amon_.] Fossil cephalopod shells.
=Am´nion= [Gr. _amnion_, fœtal membrane.] A membranous sack containing
fluid which envelopes the embryo in the classes of reptiles, birds and
mammals.
=A-mœ´ba pro´te-us= [Gr. _amoibe_, change; Proteus.] A unicellular
animal; a Protozoan.
=Am-phib´i-a= [Gr. _amphi_, double; _bios_, life.] A class of vertebrates
whose young are fish-like and have gills: the skull has two condyles and
a parasphenoid.
=Am-phi-mix´is= [Gr. _amphi_, double; _mixis_, mingling.]
=Am-phi-ox´us= [Gr. _amphi_, double; _oxys_, sharp.] A small worm-like
vertebrate whose body tapers at both ends. The skeleton is notochordal;
skull, brain, auditory, and renal organs are absent.
=An-ab´o-lism= [Gr. _ana_, up; _ballo_, throw.] Constructive metabolism;
the series of chemical changes by which a cell builds up simple and
stable food into the highly complex and unstable living material.
=An-ap-to-mor´phus= [Gr. _an_-priv.; _hapto_, fasten; _morphe_, shape.]
=An-gi-o-sper´mæ= [Gr. _angeion_, vessel; _sperma_, seed.] Plants whose
seeds are contained in a closed seed-vessel.
=An-nu-la´ta= [Lat. _annulatus_, ringed.] A division of Vermes, including
marine worms, leeches, and earthworms.
=An-the-rid´i-a= [NL., < _anthera_, anther; Gr. dim. _idion_.] The male
sexual organ in cryptogams answering to the anthers in phanerogams.
=An-thro-po-pi-the´cus= [Gr. _anthropos_, man; _pithekos_, ape.]
=An´thro-poid= [Gr. _anthropos_, man; _eidos_, form.] Manlike: said
especially of the gibbons, orangs, gorillas, and chimpanzees.
=An-ti-tox´ine= [Gr. _anti_, opposed to; _toxikon_, poison.]
=A-nu´ra= [Gr. _an_, not; _oura_, tail.] An order of amphibians without a
tail in the adult, including the toads and frogs.
=A´phis= [Gr. _apheideis_, lavish.] In Entomology a genus typical of
Aphididæ. An aphid; a plant-louse.
=Ap-pen´dix ver-mi-for´mis= [Lat. _appendo_, to hang from; _vermis_,
worm; _forma_, form.] A vestigial structure attached to commencement of
the large intestine.
=A-rach´ni-da= [Gr. _arachne_, spider.] A class of Arthropods embracing
the spiders, mites, scorpions, etc.
=Ar-cel´la= [Lat. dim. _arca_, a box.] Belonging to a group of protozoans
having a chitinous shell.
=Ar-chæ´an= [Gr. _archaios_, ancient.] Pertaining to the oldest strata of
rocks in geological history.
=Ar-chæ-op´ter-yx= [Gr. _archaios_, ancient; _pteryx_, bird.] A fossil
bird with reptilian characteristics.
=Ar-che-go-sau´rus= [Gr. _archegos_, beginning; _sauros_, lizard.] A
carboniferous amphibian (labyrinthodont.)
=Ar´go-naut= [Gr. _argo_, swift; _nautes_, sailor.]
=Ar-ma-dil´los= [Sp. dim. of _armado_, armed.] Edentate mammals having a
carapace formed by ossification of the greater part of the skin and the
union of the bony scutes.
=Ar-throp´o-da= [Gr. _arthron_, joint; _pous_, foot.] A branch of animals
(invertebrates) with jointed legs, as insects, spiders, and crabs.
=As´ter= [Gr. _aster_, star.]
=As-ter-oi´de-a= [Gr. _aster_, star; _eidos_, form.] Echinoderms having
radiating arms with ambulacral grooves below, embracing the true
star-fishes.
=At´a-vism= [Lat. _atavus_, grandfather.] Reversion; recurrence to an
ancestral type.
=At´e-les= [Gr. _ateles_, imperfect.]
=Au´ri-cles= [Lat. _auricula_, little ear.] A chamber of the heart which
receives blood from the veins and transmits it to the ventricle.
=A´ves= [Lat. pl. of _avis_, bird.] Birds, a class of vertebrata.
=Ba-cil´lus= [Lat. _bacillum_, a little stick.] A genus of bacteria
consisting of rod-like cells. They multiply by transverse division and by
the formation of endogenous spores. Unicellular plants.
=Bac-te´ri-a= [Gr. _bakterion_, stick.] Microscopic unicellular plants. A
genus of Schizomycetes (fission-fungi).
=Bal-a-no-glos´sus= [Gr. _balanos_, acorn; _glossa_, tongue.] Supposed by
some biologists to belong to the Chordata.
=Beams= [AS. _beam_, tree.] The main stem of a deer’s antler.
=Bel-em´nites= [Gr. _belemnon_, dart.] A belemnitoid cuttlefish.
=Bi´o-phores= [Gr. _bios_, life; _phero_, bear.] Biological units of
hereditary mass.
=Bi´pes= [Lat. _bis_, twice; _pes_, foot.]
=Blas´tid= [Gr. _blastos_, sprout.]
=Blas-to-ge-net´ic= [Gr. _blastos_, a germ; _genesis_, generation.]
Originating in the germ cells.
=Blas´tu-la= [Gr. _blastos_, sprout.] A stage in the growth of
the embryo; a hollow sphere of one layer of cells enclosing a
segmentation-cavity.
=Brach-i-op´o-da= [Lat. _brachium_, arm; Gr. _pous_, foot.] Molluscoid
animals with bivalve shells, one of which is dorsal and the other
ventral; also with brachial appendages coming from the sides of the
mouth. Lamp shells.
=Brach´i-o-pod= [Vid. Brachiopoda.] Lamp shell.
=Bry-oph´y-ta= [Gr. _bryon_, moss; _phyton_, plant.] A division of the
vegetable kingdom consisting of liverworts and mosses.
=Bry-o-zo´a= [Gr. _bryon_, moss; _zoon_, animal.] Moss animals.
=Ca-du-ci-bran-chi-a´ta= [Lat. _caducus_, falling; _branchia_, gills.]
Urodeles that lose their gills before maturity.
=Ca-du-ci-bran´chi-ates= [Vid. Caducibranchiata.]
=Cal´li-thrix= [Gr. _kalos_, beautiful; _thrix_, hair.]
=Cal-a-mo-ich´thys= [Gr. _kalamos_, reed; _ichthys_, fish.]
=Ca´lyx= [Gr. _kalyx_, cover.] The outermost series of leaves (sepals) of
a flower; usually green.
=Cam´bri-an= [_Cambria_, _Wales_.] The name given by Sedgwick to those
Palæozoic rocks that underly the Silurian, in Cambria (or Wales).
=Car-bon-if´er-ous= [Lat. _carbo_, coal; _fero_, bear.]
=Car-i-na´tæ= [Lat. _carinatus_, keel-shaped.] Birds having a keeled
(carinate) breast-bone.
=Car-niv´o-ra= [Lat. _caro_, flesh; _voro_, devour.] Flesh-eating mammals.
=Cas-tra´tion= [Lat. _castratus_.] Removal of the glands that bear the
Germ-Cells.
=Cat-ar-rhi´næ= [Gr. _kata_, down; _rhis_, nose.] Old World monkeys. The
septum of the nose is narrow; the tail is short and not prehensile.
=Cat´ar-rhines= [Vid. Catarrhinæ.] Old World monkeys.
=Ceb´i-dæ= [Gr. _kebos_, long-tailed monkey.] A family of New World
monkeys.
=Ce´bus= [Gr. _kebos_, long-tailed monkey.]
=Cen-o-zo´ic= [Gr. _kainos_, new; _zoe_, life.] Relating to the
Quaternary and Tertiary eras.
=Cen´ti-pede= [Lat. _centum_, hundred; _pes_, foot.] A many jointed
myriapod having a pair of legs to each joint.
=Cen´tro-some= [Gr. _kentron_, center; _soma_, body.] A body just outside
of the nucleus of a cell and that governs the mitotic phases of a cell.
=Ceph-a-lop´o-da= [Gr. _kephale_, head; _pous_, foot.] Molluscs with a
subcentral head, a beaked mouth, and tentacles taking the place of feet,
including cuttlefishes, etc.
=Cer´a-tites= [Gr. _keras_, horn; _ites_, like.] A fossil cephalopod with
the habitation chamber short and sutural saddles mostly simple.
=Cer´a-to-dus= [Gr. _keras_, horn; _odous_, tooth.] So-called from the
horn-like ridges of the teeth. A lung-fish.
=Cer-co-pi-the´ci-dæ= [Gr. _kerkopithekos_, a long-tailed ape; _eidos_
form.] A family of catarrhine anthropoidea.
=Cer-e-bel´lum= [Lat. dim. of _cerebrum_, brain.] A subdivision of the
encephalon.
=Cer´e-brum= [Lat. brain.] A subdivision of the encephalon.
=Cer´e-bral= [Vid. Cerebrum.] Pertaining to the cerebrum.
=Ce-ta´ce-a= [Lat. _cetus_, whale.] An order of fish-like mammals
including the whales and porpoises.
=Chei-rop´te-ra= [Gr. _cheir_, hand; _pteron_, wing.] Including the
Bats,—an order of mammals.
=Chei-ro´tes= [Gr. _cheirotos_, having a hand.] A native lizard of Mexico.
=Che-lo´ni-a= [Gr. _chelone_, tortoise.] An order of reptiles, including
the turtles and tortoises.
=Chi-mæ´roids= [Gr. _chimaira_, a fabled monster; _eidos_, form.] An
order of elasmobranchii (holocephali) with opercular membrane and smooth
skin.
=Chi´ro-mys= [Gr. _cheir_, hand; _mus_, mouse.]
=Chim-pan´zee= [W. Afr.] Anthropopithecus. A West African arboreal,
anthropoid ape; five feet high; distinct eyelashes, eyebrows, and
whiskers; very large ears. It approximates to man in its dentition and
the length of its arms. Has darker hair than gorilla.
=Chi´tin-ous= [Gr. _chiton_, tunic.] Pertaining to chitin, the horny
substance in the skin of insects.
=Chro´ma-tin= [Gr. _croma_, color.] Nuclear threads.
=Chor-da´ta= [Lat. _chorda_, chord.] A subkingdom of animals with a
notochord persistent or evanescent.
=Chro´mo-somes= [Gr. _croma_, color: _soma_, body.] Nuclear threads.
=Chry´so-thrix= [Gr. _chrysos_, gold; _thrix_, hair.]
=Clo-a´ca= [Lat. _cloaca_, a common sewer.] The common cavity into which
the digestive, urinary, and genital canals empty in most vertebrates
below placentals, and in all mammalian embryos.
=Coc´ci= [Gr. _kokkos_, berry.] Pl. of _coccus_. Isolated spherical cells
(bacteria).
=Co-coons´= [F. _cocon_, dim. of _coque_, shell; < Lat. _concha_, shell.]
The protective envelopes spun by certain larval insects, as silkworms, in
which they are inclosed in the chrysalis state.
=Co-do-si´ga um-bel-la´ta= [Gr. _kodon_, a bell; _sige_, silence; Lat.
_umbella_, dim. of _umbra_, shade.]
=Cœ-cil´i-a= [Lat. _cæcus_, blind.] Footless amphibians of snake-like
form; rudimentary eyes; no neck.
=Cœ-len-te-ra´ta= [Gr. _koilos_, hollow; _enteron_, intestine.]
=Cœ-len´ter-ate= [Vid. Cœlenterata.]
=Cϫlome= [Gr. _koilos_, hollow.] The body-cavity of a metazoan between
the viscera and the body-wall.
=Combs= [AS. _camb_, crest or ridge.] The fleshy crests on the heads of
roosters, etc.
=Con-dy-lar´thra= [Gr. _kondylos_, knuckle; _arthron_, joint.] An Eocene
group of ungulates in which the astragalus is not interlocked laterally
with the tibia and its head rounded.
=Co-nif´e-ræ= [Lat. _conus_, cone; _fero_, bear.] The pine family of
trees.
=Co´nus ar-te-ri-o´sus= [_Latin phrase_.] The arterial, cone-shaped
portion of the left ventricle of the heart.
=Co-rol´la= [Lat., dim. of _corona_, crown.] The inner set of leaves
of flowers and usually bright-colored. The individual parts are called
petals.
=Crests= [Lat. _crista_, tuft.] Projecting natural growths on the tops
of animals’ heads and usually ornamental, as the cock’s comb, or the
lengthened feathers of a bird.
=Cre-o-don´ta= [Gr. _kreas_, flesh; _odous_, tooth.] A group of fossil
animals containing forms ancestrally related to existing Carnivora.
=Cre-ta´ceous= [Lat. _creta_, chalk.] Pertaining to the latter part of
the Reptilian age.
=Cri-noi´de-a= [Gr. _krinon_, lily; _eidos_, form.] Stone-lilies; stalked
star-fishes. A division of Echinoderms.
=Cri´noids= [Vid. Crinoidea.]
=Croc-o-dil´i-a= [Lat. _crocodilus_, lizard.] An order of reptiles
including crocodiles, alligators, and gavials. They are the highest order
of reptiles. In them the heart and brain approximate very closely to that
of birds.
=Cros-sop-te-ryg´i-a= [Gr. _krossoi_, tassels; _pterygion_ dim. of
_pteryx_, wing.] A group of fishes with paired, lobate fins, and with an
endodermal skeletal, axis fringed with dermal rays.
=Crus-ta´ce-a= [Lat. _crusta_, crust.] A division of arthropods
containing crabs, lobsters, shrimps, crawfish, barnacles, etc.
=Cryp´to-gams= [Gr. _kryptos_, hidden; _gamos_, marriage.] The lower
of the two great subdivisions of the plant kingdom. They have no true
flowers containing stamens, pistils, and seeds; they propagate by means
of spores.
=Cten-oph´o-ra= [Gr. _kteis_, comb; _phero_, bear.] A subdivision of
cœlenterates with paddle-like locomotive plates arranged in eight
meridional rows on the outer surface of the body.
=Cyc-a-da´ce-æ= [Gr. _kykos_, African coco-palm.] The cycad family of
plants (gymnospermous), of fern-like or palm-like aspect.
=Cys-toi´de-a= [Gr. _kystis_, bladder; _eidos_, form.]
=Cy-no-ceph´a-lus= [Gr. _kyon_, dog; _kephale_, head.]
=Cy´to-plasm= [Gr. _kyo_, be pregnant; _plasma_, < _plasso_, form.]
Protoplasm; especially that portion of a cell apart from the nucleus.
=Dal´ton-ism= [Dalton, chemist, who had color-blindness.]
Color-blindness, especially red-blindness.
=De-cid´u-ate= [Lat. _deciduus_, falling off.] Shed at periodic times.
=Des´mids= [Gr. _desmos_, band.] Unicellular plants of minute size;
bright-green in color; mainly solitary, fresh-water algæ.
=Dev-o´ni-an= [Devonshire, England.] The name given by Murchison to
Palæozoic rocks in Devonshire, England.
=Di´a-toms= [Gr. _dia_, through; _tome_, cutting.] Microscopic
unicellular algæ inhabiting salt or fresh water. Each individual
(frustule) consists of two flint valves which are more or less
symmetrical. They are either isolated or attached together in a series.
=Di-cot-y-le´don-es= [Gr. _dikotylos_, with two hollows.] The most
important and largest class of flowering plants. Characterized by
having seeds with two cotyledons, exogenous stems, and leaves that are
netted-veined; the parts of the flower mostly in fours or fives.
=Di-del´phi-a= [Gr. _di_-, two; _delphys_, womb.] A sub-class of mammals,
as the Marsupials, having a double womb and no placenta.
=Dif-flu´gi-a pyri-form´is= [Lat. _diffluere_, to flow apart; _pyrum_,
pear; _forma_, form.]
=Di-no-sau´ri-a= [Gr. _deinos_, terrible; _sauros_, lizard.] Mesozoic
land reptiles.
=Dip´no-i= [Gr. _di_-, two; _pneo_, breathe.] Fishes with regular gills,
a double or single lung, and nostrils inside as well as outside the
mouth.
=Dro-ma-the´ri-um= [Gr. _dromos_, running; _therion_, small wild beast.]
=Dys-chro-ma-top´si-a= [Gr. _dys_, bad; _chroma_, color; _opsis_, sight.]
Partial color-blindness; difficulty in distinguishing colors.
=E-chi-no-der´ma-ta= [Gr. _echinos_, hedgehog; _derma_, skin.]
=E-chi´no-derms= [Vid. Echinodermata.]
=Ech-i-noi´de-a= [Gr. _echinos_, hedgehog; _eidos_, form.] Echinoderms
including sea urchins.
=Ec´to-derm= [Gr. _ektos_, outside; _derma_, skin.]
=Ec´to-plasm= [Gr. _ektos_, outside; _plasso_, form.]
=E-den-ta´ta= [Lat. _e_, out of; _dens_, tooth.] An order of placentals
with a small, one-lobed cerebrum; without median, cutting teeth:
including armadillos, ant-eaters, and sloths.
=El-as-mo-bran´chi-i= [Gr. _elasmos_, metal plate; _branchia_, gills.]
Fish-like vertebrates which have no membrane bones in the skull or the
shoulder-girdle; five pairs of strap-like gills attached by their distal
ends; claspers to the ventral fins of males; complicated brain with optic
nerves forming a decussation.
=Em´bry-o= [Gr. _en_, in; _bruein_, swell.] The term applied to an animal
in the earlier stages of development.
=Em-bry-ol´o-gy= [Gr. _embryon_, embryo; _logos_, < _lego_, speak.] The
study of embryos.
=En´do-derm= [Gr. _endon_, within; _derma_, skin.]
=En´do-plasm= [Gr. _endon_, within; _plasso_, form.]
=En-ter-op-neus´ta= [Gr. _enteron_, intestine; _pneustos_, breathing.]
Acorn-tongue worms. Smooth-bodied, footless worms, having a large
exserted soft proboscis; breathing by a series of respiratory sacs
opening into the digestive canal, and communicating externally
by spiracles; nervous system situated above a seeming notochord.
Balanoglossus. Included by some biologists among the chordata.
=E-o-hip´pus= [Gr. _eos_. dawn; _hippos_, horse.]
=E´o-cene= [Gr. _eos_, dawn; _kainos_, recent.]
=Ep-en-ceph´a-lon= [Gr. _epi_, upon; _enkephalos_, brain.] A fundamental
subdivision of the brain (encephalon).
=Ep´i-blast= [Gr. _epi_, upon; _blastos_, bud.]
=E´quus= [Lat. horse.]
=E-ryth-ro-lam´prus= [Gr. _erythros_, red; _lampros_, shining.]
=Eu-ca-lyp´tus= [Gr. _eu_, good; _kalypto_, cover.] A large genus of
evergreen trees of the myrtle family.
=Ev-o-lu´tion= [Lat. _e_, out; _volvo_, roll.]
=Ex-o-skel´e-ton= [Gr. _exo_, outside; _skeleton_, dried body.] External
skeleton; bony or horny hardening of the integument.
=Fla-gel´lum= [Lat., dim. of _flagrum_, scourge.] A slender protoplasmic
extension of a cell, for purposes of locomotion.
=Fo-ram-i-nif´e-ra= [Lat. _foramen_, opening; _fero_, bear.] A division
of protozoans secreting a shell perforated by many minute apertures.
=Fos´sil= [Lat. _fodio_, dig.] Any organic body so situated in the earth,
and so buried in solid rock or in earthy deposits, as to be capable of
indefinite preservation.
=Gan´gli-on= [Gr. _ganglion_, tumor.] A swelling that consists of an
aggregation of nerve-cells. It receives and discharges nervous impulses
and serves to stimulate psychical and organic activities.
=Ga-noi´de-i= [Gr. _ganos_, brightness; _eidos_, appearance.]
=Gas-ter-op´o-da= [Gr. _gaster_, stomach; _pous_, foot.] Including all
snails and slugs.
=Gas´tru-la= [Dim. of Lat. _gaster_, stomach.]
=Gem´mæ= [Lat. buds.]
=Geph-y-re´a= [Gr. _gephyra_, bridge.] A division of worms with an
œsophageal nervous ring and ventral chord; no distinct segments or legs;
a terminal or dorsal anus.
=Go´ni-a-tites= [Gr. _gonia_, corner; _lithos_, stone.] A genus of fossil
Ammonites.
=Gor´gets= [Fr. _gorgette_, dim. of _gorge_, throat.] Throat-patches
distinguished by color or texture, especially in humming birds.
=Grap´to-lites= [Gr. _graptos_, written; _lithos_, stone.] Fossil
hydroids.
=Greg-a-ri´na= [Lat. _gregarius_, < _grex_, flock.] A genus typical of
Gregarinidæ. _Gregarina gigantea_ is sixteen millimeters in length and is
one of the largest unicellular animals known.
=Greg-a-rin´i-dæ= [Vid. Gregarina.] More or less elongated amœba-like
Protozoa, having a well-defined cell-wall, and a “subcuticular” system
of muscular fibrillæ; nucleus, but no contractile vacuole; reproduction
by encystment and subdivision of the central cell mass or protoplasm, by
which shelly psorosperms are formed and from which escape the moner-like
young, which undergo a metamorphosis.
=Gro´mi-a o-vi-form´is= [Lat. _gromia_; _ovum_, egg; _forma_, form.] A
characteristic imperforate foraminifer.
=Gym-no-phi´o-na= [Gr. _gymnos_, naked; _ophis_, serpent]
=Gym-no-sper´mæ= [Gr. _gymnos_, naked; _sperma_, seed.] Plants whose
seeds are not contained in a closed seed-vessel, as Cycads and Conifers.
=Hap´a-le= [Gr. _hapalos_, gentle.]
=Ha-pal´i-dæ= [Gr. _hapalos_, gentle] A family of New World monkeys
including the Marmosets.
=Hel-i-co-nid´æ= [N., < _heliconius_, of Helicon; idæ.] A family of
butterflies.
=Hes-per-or´nis= [Gr. _hesperos_, western; _ornis_, bird.] Cretaceous
carinate birds with rudimentary wings, short tail, and pointed teeth
implanted in grooves.
=Hip-po-pot´a-mus= [Gr. _hippos_, horse; _potamos_, river.]
=Hol-o-ceph´a-li= [Gr. _holos_, whole; _kepale_, head.] A subdivision of
Elasmobranchii in which the suspensorium of the lower jaw is continuous
with the cranium, as chimæroids, etc.
=Hol-o-thu-roi´de-a= [Gr. _holos_, whole; _thouros_, rushing.] Worm-like
echinoderms, with skin-like integuments, and circum-oral tentacles;
including sea-cucumbers, sea-slugs, etc.
=Ho-min´i-dæ= [Lat. _homo_, man; idæ.] A family of primates restricted to
mankind.
=Hy´a-lo-plasm= [Gr. _hyalos_, glass; _plasma_, < _plasso_, form.]
=Hy´dra= [Gr. _hydra_, Lernæan serpent, < _hudor_, water.] A fresh-water
polyp, having the form of a cylindrical tube, surrounded at the mouth
with a circle of thread-like tentacles, by which it captures its prey.
=Hy´droid= [Gr. _hudor_, water; _eidos_, form.] Resembling the _hydra_;
pertaining to the Hydroidea.
=Hy-dro-zo´a= [Hydro-; _zoon_, animal.] Cœlenterates including Hydroids
and jelly-fishes.
=Hy-lob-a-ti´næ= [Gr. _hylobates_, one who walks the wood.] An Asiatic
subfamily of apes; the long-armed apes or gibbons.
=Hy-lob´a-tes= [Gr. _hylobates_.] A gibbon,—an Asiatic ape.
=Hy-ra-coi´de-a= [Gr. _hyrax_, shrew-mouse; _eidos_, appearance.]
=Ich-thy-or´nis= [Gr. _ichthys_, fish; _ornis_, bird.] Cretaceous
toothed birds of tern-like form, with socketed acute teeth, and
bi-concave vertebræ
=Ich-thy-o-sau´ri-a= [Gr. _ichthys_, fish; _sauros_, lizard.]
=Id´i-o-blast= [Gr. _idios_, individual; _blastema_, sprout.]
=In-fu-so´ri-a= [Lat. _in_, into; _fundo_, pour.] So called because
including many animalcules that occur in infusions of decaying substances.
=In-sec´ta= [Lat. _in_, into; _seco_, cut.]
=In-sec-tiv´o-ra= [Lat. _insectum_, insect; _voro_, devour.]
=In-ver-te-bra´ta= [Lat. _in_, not; _vertebratus_, jointed.] Including
all animals that do not possess a notochord or backbone: opposed to
Vertebrata.
=In-ver´te-brates= [Vid. Invertebrata.]
=Ju-ras´sic= [Jura mountains.]
=Kaf´ir-boom= [Erythrina caffra.] A prickly-stemmed tree of South Africa.
=Kal´li-ma para-lek´ta= [Gr. _kallimos_, beautiful; _para_, along side
of; _lektos_, picked out.]
=Keri-vou´la pic´ta.=
=Lab-y-rin´tho-donts= [Gr. _labyrinthos_, labyrinth; _odous_, tooth.]
Extinct amphibians.
=Lac-er-til´i-a= [Lat. _lacertus_, lizard.]
=La-ge´na= [Gr. _lagynos_, flask.]
=La-mel-li-bran-chi-a´ta= [Lat. _lamella_, a plate; _branchia_, gills.]
Bivalve molluscs.
=La-nu´go= [Lat. _lana_, wool.]
=Lar´væ= [Lat. pl. of _larva_, mask.] The early forms of animals when
they are unlike the parent. In insects the first stages after leaving the
eggs, preceding the pupa, as maggots or caterpillars.
=Lem-u-roi´de-a= [Lemur; Gr. _eidos_, appearance.] A sub order of
Primates. Prosimiæ.
=Lep-i-do-si´ren= [Gr. _lepis_, scale; _siren_, a genus of amphibians.]
One of the lung-fishes.
=Lep-to-car´di-i= [Gr. _leptos_, fine, small; _kardia_, heart.]
=Liv´er-worts.=
=Lon-gi-cor´ni-a= [Lat. _longus_, long; _cornu_, horn.] A division of
beetles having very long filiform antennæ.
=Ma-caques´= [F., < Afr. _macaquo_.] Cercopithecine monkeys of the genus
_macacus_. Their form is stout; large ischial tuberosities: muzzle
considerably produced.
=Ma-ca´cus.=
=Mam´mal= [Lat. _mamma_, breast; suffix -_al_; in analogy with
Animal. Dr. Th. Gill.] Vertebrate animal whose female has mammæ, or
milk-secreting organs.
=Mam-ma´li-a= [Vid. mammal.]
=Man´tis= [Gr. _mantis_, prophet.] The mantises are insects noted for the
manner in which they carry the large spinous fore legs when waiting for
prey. They have the attitude, then, as if praying.
=Mar´mo-set.= A small South-American monkey.
=Mar-si-po-bran´chi-i= [Gr. _marsipos_, bag; _branchia_, gills.]
=Mar-su´pi-al= [Lat. _marsupium_, pouch.] Animals having a marsupium or
pouch for retaining the young.
=Mas´to-don= [Gr. _mastos_, breast; _odous_, tooth.] An extinct elephant.
=Me-dul´la= [Lat. _medius_, middle.] A subdivision of the brain—that
portion especially that is continuous with the spinal chord.
=Men-o-bran´chus= [Gr. _meno_, remain; _branchia_, gills.] A large
American aquatic amphibian, of salamander-like form, with persistent
gills, as the mud-puppy.
=Mens sana in corpore sano.= A Latin phrase meaning a sound mind in a
sound body.
=Mes-en-ceph´a-lon= [Gr. _mesos_, middle; _enkephalos_, brain.] A
fundamental segment of the brain.
=Mes´en-chyme= [Gr. _mesos_, middle; _enchyma_, infusion.]
=Mes´o-blast= [Gr. _mesos_, middle; _blastos_, germ.]
=Mes-o-glϫa= [Gr. _mesos_, middle; _gloia_, glue.]
=Mes-o-hip´pus= [Gr. _mesos_, middle; _hippos_, horse.]
=Mes-o-zo´ic= [Gr. _mesos_, middle; _zoe_, life.]
=Met-a-dis-coi´dal= [Gr. _meta_, after; _diskos_, disk; _eidos_,
appearance.] Resembling a discoidal form.
=Met-a-mor´pho-sis= [Gr. _meta_, over; _morphe_, form.] The series of
pronounced external changes through which an animal passes after leaving
the egg-envelopes and before reaching sexual maturity.
=Met-a-phy´ta= [Gr. _meta_, above, higher; _phyton_, plant.]
=Met´a-plasm= [Gr. _metaplasmos_, transformation.]
=Met-a-zo´a= [Gr. _meta_, after, higher; _zoon_, animal.]
=Met-en-ceph´a-lon= [Gr. _meta_, after; _enkephalos_, brain.] A
fundamental segment of the brain.
=Mi-cro-ceph-a´li-a= [Gr. _mikrokephalos_, small-headed.] Imperfect
development of the cranium.
=Mi-cren-ceph-a´li-a= [Gr. _mikros_, small; _enkephalos_, brain.]
Small-brained.
=Mi´cro-cosm= [Gr. _mikros_, small; _kosmos_, world.]
=Micro-gro´mi-a so-ci-al´is= [Gr. _mikros_, small; _gromia_; Lat.
_socialis_ < _socius_, companion.]
=Mi-cro-les´tes.=
=Mi´das.= A wealthy king of Phrygia.
=Mi-o-hip´pus= [Miocene; Gr. _hippos_, horse.]
=Mi´o-cene= [Gr. _meion_, less; _kainos_, recent.]
=Mi-to´sis= [Gr. _mitos_, thread.]
=Mol-lus´ca= [Lat. _mollis_, soft.]
=Mon-o-cot-y-le´don-es= [Gr. _monos_, single; _kotyledon_, cup-shaped
cavity.] A group of flowering plants in which the first leaves of
the embryo are alternate, for which reason they are said to have one
seed-leaf or cotyledon.
=Mon-o-del´phi-a= [Gr. _monos_, single; _delphys_, womb.] A sub-class of
mammals having a single vagina and uterus; embryo attached by a placenta;
brain has a corpus callosum. Includes all animals above Monotremes and
Marsupials.
=Mon´o-tremes= [Gr. _monos_, single; _trema_, hole.] An order of
ornithodelphians.
=Mor´u-la= [Lat. dim. of _morum_, mulberry.]
=Mul-ti-tu-ber-cu-la´ta= [Lat. _multus_, many; _tuberculum_, tubercle.]
=My-ce´tes= [Gr. _myketes_, bellower.]
=Myr-i-ap´o-da= [Gr. _myrios_, numberless; _pous_, foot.] Insects with
numerous pairs of legs, as centipedes.
=Nau´ti-loids= [Gr. _nautilos_, sailor; _eidos_, like.] A group of
cephalopods.
=Nau´ti-lus= [Gr. _nautilos_, sailor.] A cephalopod.
=Nem-a-thel-min´thes= [Gr. _nema_, thread; _helmins_, worm.]
=Nem-er-ti´na= [Gr. _nemertes_, unerring.] Worms with skin ciliated,
proboscis retractile, and nervous, muscular, and vascular systems
characteristically developed.
=Ne-o-lith´ic= [Gr. _neos_, new; _lithos_, stone.]
=Noc-ti-lu´ca mi-li-a´ris= [Lat. _nox_, night; _luceo_, shine;
_miliarius_, < _milium_, millet.]
=No´to-chord= [Gr. _notos_, the back; _chorda_, a chord.] A cartilaginous
rod found in the young chordate embryo in a situation that is later
on occupied by the centers of the bodies of the vertebræ. It separates
a dorsal nervous system from a ventral alimentary (digestive) canal.
The notochord is persistent in its entirety in Leptocardians and
Marsipobranchs and also in some pisces, as the sturgeon.
=O-don-tor´ni-thes= [Gr. _odous_, a tooth; _ornis_, bird.] Including all
those extinct birds having teeth.
=Œ-soph´a-gus= [Gr. _oiso_, will bear; _phagein_, eat.] The gullet; the
membranous tube through which food passes from the pharynx to the stomach.
=On-tog´e-ny= [Gr. _on_, being; _genesis_, origin.] The history of the
evolution of the individual; the development of the individual.
=On-to-ge-net´ic= [Gr. _on_, being; _genesis_, origin.] Pertaining to
ontogeny.
=On-y-choph´o-ra= [Gr. _onyx_, claw; _pherein_, bear.] Arthropods
including only a single genus, the curious caterpillar-like Peripatus.
=Oösperm= [Gr. _oon_, egg; _sperma_, semen.] A fertilized ovum. The first
stage in the existence of a human being is called oösperm.
=O-per´cu-lum= [Lat. lid.] The gill-cover.
=O-phid´i-a= [Gr. _ophis_, serpent.] Serpents; snakes.
=Op-po´nens Hal-lu´cis= [Lat. _ob_, _pono_, to place over against;
_hallux_, great toe.] The name of a muscle in the foot.
=Or-do-vi´cian= [_ordovices_, ancient Celtic tribe in Wales.]
=Or-nith-o-del´phi-a= [Gr. _ornis_, bird; _delphys_, womb.] A sub-class
of oviparous mammals.
=Or-o-hip´pus= [Gr. _oros_, mountain; _hippos_, horse.]
=Or-tho-cer´a-tites= [Gr. _orthos_, straight; _keras_, horn.]
=Os´te-o-blasts= [Gr. _osteon_, bone; _blastano_, sprout.]
=Os´te-o-clasts= [Gr. _osteon_, bone; _klao_, destroy.]
=Os´tra-co-derms= [Gr. _ostrakon_, shell; _derma_, skin.]
=Ovum= [Lat. _egg_.] Female germ-cell; female, encysted, sexual cell.
=O-vip´a-rous= [Lat. _ovum_, egg; _pairo_, produce.] Producing eggs that
mature and are hatched outside the body.
=Pal´li-um= [Gr. _mantle_.]
=Pa-læ-o-lith´ic= [Gr. _palaios_, ancient; _lithos_, stone.]
=Pa-læ-o-zo´ic= [Gr. _palaios_, ancient; _zoe_, life.]
=Pan-do-ri´na mor´um= [Gr. Pandora; _moron_, mulberry.]
=Pan-gen´e-sis= [Gr. _pas_, all; _genesis_, origin.]
=Par-a-me´ci-um= [Gr. _paramekes_, of longish shape.]
=Par-then-o-gen´e-sis= [Gr. _parthenos_, virgin; _genesis_, origin.]
Production of a new individual from a virgin female without intervention
of a male; reproduction by means of unfertilized eggs.
=Per-en-ni-bran-chi-a´ta= [Lat. _perennis_, perpetual; _branchia_, gills.]
=Per-en-ni-bran´chi-ates= [Vid. Perennibranchiata.]
=Ped´al= [Lat. _pes_, foot.]
=Per´mi-an= [Perm, Russia.]
=Phan´er-o-gams= [Gr. _phaneros_, visible; _gamos_, marriage.] Flowering
plants.
=Phos-phor-es´cence.=
=Phryn-o-ceph´a-lus mys-ta´ce-us.=
=Phy-log´e-ny= [Gr. _phylon_, tribe; _genesis_, origin.] The history of
the evolution of a species or group; distinguished from ontogeny.
=Phy-lo-ge-net´ic= [Vid. phylogeny.] Pertaining to phylogeny.
=Pith´e-coid= [Gr. _pithekos_, ape; _eidos_, like.]
=Pith-e-can-thro´pus= [Gr. _pithekos_, ape; _anthropos_, man.]
=Pla-gi-os´to-mi= [Gr. _plagios_, oblique; _stoma_, mouth.] A division of
Elasmobranchii, including sharks and rays.
=Pla-cen´tal= [Lat. _placenta_, cake.] So called on account of its
shape. Pertaining to the _placenta_, the organ of attachment of higher
vertebrate (monodelph) embryos to the wall of the uterus of the female.
=Plas´tids= [Gr. _plastos_, formed.]
=Plat-y-hel-min´thes= [Gr. _platys_, flat; _helminos_, worm.]
=Plat-y-rhi´næ= [Gr. _platys_, broad, flat; _rhis_, nose.] Monkeys of the
New World having long tails and a wide septum to the nose.
=Pleur-a-can´thus= [Gr. _pleuron_, rib; _akantha_, thorn.]
=Pleu´ral= [Gr. _pleura_, rib, side.]
=Pli-o-hip´pus= [Pliocene; Gr. _hippos_, horse.]
=Pli´o-cene= [Gr. _pleion_, more; _kainos_, recent.]
=Plumes= [Lat. _pluma_, small soft feather.] Feathers, especially when
ornamental or large; or tufts of large and ornamental feathers.
=Pneu-mo-coc´ci= [Gr. _pneumon_, lung; _kokkos_, berry.] Bacteria
(spheroidal) found in those suffering from pneumonia.
=Pol-y-dac´tyl-ism= [Gr. _polys_, many; _daktylos_, finger, toe.] The
possession of an abnormally large number of fingers or toes.
=Pol-y-mor´phism= [Gr. _polys_, many; _morphe_, form.] Exhibition by a
group of animals, as a species, of different types of form or structure.
=Po-lyp´te-rus= [Gr. _polypteros_, many-winged.]
=Po-ly´o-don= [Gr. _polys_, many; _odous_, tooth.]
=Pol´yp= [Gr. _polys_, many; _pous_, foot.]
=Pol´y-the-ism= [Gr. _polys_, many; _theos_, god.]
=Po-rif´e-ra= [Lat. _porus_, pore; _fero_, bear.]
=Pre-Pa-læ-o-lith´ic= [Lat. _præ_, before; Palæolithic.] The period of
time preceding the Ancient Stone Age.
=Pri-ma´tes= [Lat. _primus_, first.] An order of mammals.
=Pro-bos-cid´e-a= [Gr. _pro_, before; _bosko_, feed.]
=Pro-nu´cle-us= [Lat. _pro_, before; _nucleus_, kernel.]
=Pros-en-ceph´a-lon= [Gr. _pro_, before; _enkephalos_, brain.] A
fundamental segment of the brain.
=Pro-to-hip´pus= [Gr. _protos_, first; _hippos_, horse.]
=Pro-toph´y-ta= [Gr. _protos_, first; _phyton_, plant.]
=Pro´to-plasm= [Gr. _protos_, first; _plasma_, < _plasso_, form.]
=Pro-top´te-rus= [Gr. _protos_, first; _pteron_, wing.]
=Pro-to-zo´a= [Gr. _protos_, first; _zoon_, animal.]
=Pseu-do-he-red´i-ty= [Gr. _pseudes_, false; Lat. _heredita_, heirship.]
=Pseu-do-po´di-a= [Gr. _pseudes_, false; _pous_, foot.]
=Psy-cho-zo´ic= [Gr. _psyche_, soul; _zoe_, life.]