We come now to the Halcyonoids, represented in our waters by the

Halcyonium (Fig. 22). In the Halcyonoids, the highest group of Polyps,

the tentacles reach their greatest limitation, which, as above

mentioned, is found to be a mark of superiority, and, connected with

other structural features, places them at the head of their class. The

number of tentacles throughout this group is always eight. They are

very complicated (Fig. 21), in comparison with the tentacles of the

lower orders, being deeply lobed, and fringed around the margin. Our

Halcyonium communities (Fig. 22) usually live in deep water, attached

to dead shells, though they may occasionally be found growing at

low-water mark, but this is very rare. They have received a rather

lugubrious name from the fishermen, who call them "dead-men's

fingers," and indeed, when the animals are contracted, such a

community, with its short branches attached to the main stock, looks

not unlike the stump of a hand, with short, fat fingers. In such a

condition they are very ugly, the whole mass being somewhat gelatinous

in texture, and a dull, yellowish pink in color. But when the animals,

which are capable of great extension, are fully spread, as in Fig. 22,

such a polyp-stock has a mossy, tufted look, and is by no means an

unsightly object. When the individuals are entirely expanded, as in

Fig. 23, they become quite transparent, and their internal structure

can readily be seen through the walls of the body; we can then easily

distinguish the digestive cavity, supported for its whole length by

the eight radiating partitions, as well as the great size of the main

digestive cavity surrounding it. Notwithstanding the remarkable power

of contraction and dilatation in the animals themselves, the tentacles

are but slightly contractile. This kind of community increases

altogether by budding, the individual polyps remaining more or less

united, the tissues of the individuals becoming thicker by the

deposition of lime nodules, and thus forming a massive

semi-cartilaginous pulp, uniting the whole community. In the

neighborhood of Provincetown they are very plentiful, and are found

all along the shores of our Bay in deep water.

[Illustration: Fig. 22. Halcyonium community; natural size.]

[Illustration: Fig. 23. Individual of Halcyonium fully expanded;

magnified.]

GENERAL SKETCH OF ACALEPHS.

In the whole history of metamorphosis, that wonderful chapter in the

life of animals, there is nothing more strange or more interesting

than the transformations of the Acalephs. First, as little floating

planulæ or transparent spheres, covered with fine vibratile cilia, by

means of which they move with great rapidity, then as communities

fixed to the ground and increasing by budding like the corals, or

multiplying by self-division, and later as free-swimming Jelly-fishes,

many of them pass through phases which have long baffled the

investigations of naturalists, and have only recently been understood

in their true connection. Great progress has, however, been made

during this century in our knowledge of this class. Thanks to the

investigations of Sars, Dujardin, Steenstrup, Van Beneden, and many

others, we now have the key to their true relations, and transient

phases of growth, long believed to be the adult condition of distinct

animals, are recognized as parts in a cycle of development belonging

to one and the same life. As the class now stands, it includes three

orders, highest among which are the CTENOPHORÆ, so called on account

of their locomotive organs, consisting of minute flappers arranged in

vertical comb-like rows; next to these are the DISCOPHORÆ, with their

large gelatinous umbrella-like disks, commonly called Jelly-fishes,

Sun-fishes, or Sea-blubbers, and below these come the HYDROIDS,

embracing the most minute and most diversified of all these animals.

These orders are distinguished not only by their striking external

differences, but by their mode of development also. The Ctenophoræ

grow from eggs by a direct continuous process of development, without

undergoing any striking metamorphosis; the Discophoræ, with some few

exceptions, in which they develop like the Ctenophoræ from eggs, begin

life as a Hydra-like animal, the subsequent self-division of which

gives rise, by a singular process, presently to be described, to a

number of distinct Jelly-fishes; the Hydroids include all those

Acalephs which either pass the earlier stages of their existence as

little shrub-like communities, or remain in that condition through

life. These Hydroid stocks, as they are sometimes called, give rise to

buds; these buds are transformed into Jelly-fishes, which in some

instances break off when mature and swim away as free animals, while

in others they remain permanent members of the Hydroid stock, never

assuming a free mode of life. All these buds when mature, whether free

or fixed, lay eggs in their turn, from which a fresh stock arises to

renew this singular cycle of growth, known among naturalists as

"alternate generations."

[Illustration: Fig. 24. Branch of Millepora alcicornis; natural

size. (_Agassiz_.)]

[Illustration: Fig. 25. Animals of M. alcicornis expanded;

magnified. _a_ _a_ _a_ small Hydroid, _b_ larger Hydroid, _t_

tentacles, _m_ mouth. (_Agassiz_.)]

The Hydroids are not all attached to the ground,--some like the

Physalia (Portuguese man-of-war), or the Nanomia, that pretty floating

Hydroid of our own waters, move about with as much freedom as if they

enjoyed an individual independent existence. As all these orders have

their representatives on our coast, to be described hereafter in

detail, we need only allude here to their characteristic features. But

we must not leave unnoticed one very remarkable Hydroid Acaleph (Fig.

24), not found in our waters, and resembling the Polyps so much, that

it has long been associated with them. The Millepore is a coral, and

was therefore the more easily confounded with the Polyps, so large a

proportion of which build coral stocks; but a more minute

investigation of its structure (Figs. 25, 26) has recently shown that

it belongs with the Acalephs.[2] This discovery is the more important,

not only as explaining the true position of this animal in the Animal

Kingdom, but as proving also the presence of Acalephs in the earliest

periods of creation, since it refers a large number of fossil corals,

whose affinities with the millepores are well understood, to that

class, instead of to the class of Polyps with which they had hitherto

been associated. But for this we should have no positive evidence of

the existence of Acalephs in early geological periods, the gelatinous

texture of the ordinary Jelly-fishes making their preservation almost

impossible. It is not strange that the true nature of this animal

should have remained so long unexplained; for it is only by the soft

parts of the body, not of course preserved in the fossil condition,

that their relations to the Acalephs may be detected; and they are so

shy of approach, drawing their tentacles and the upper part of the

body into their limestone frame if disturbed, that it is not easy to

examine the living animal.

[Footnote 2: See "Methods of Study," by Prof. Agassiz.]

[Illustration: Fig. 26. Transverse section of a branch, showing

pits, _a_ _a_ _a_ _a_, of the large Hydroids with the horizontal

floors. (_Agassiz_.)]

The Millepore is very abundant on the Florida reefs. From the solid

base of the coral stock arise broad ridges, branching more or less

along the edges, the whole surface being covered by innumerable pores,

from which the diminutive animals project when expanded. (Fig. 25.)

The whole mass of the coral is porous, and the cavities occupied by

the Hydræ are sunk perpendicularly to the surface within the stock.

Seen in a transverse cut these tubular cavities are divided at

intervals by horizontal partitions (Fig. 26), extending straight

across the cavity from wall to wall, and closing it up entirely, the

animal occupying only the outer-most open space, and building a new

partition behind it as it rises in the process of growth. This

structure is totally different from that of the Madrepores, Astræans,

Porites, and indeed, from all the polyp corals which, like all Polyps,

have the vertical partitions running through the whole length of the

body, and more or less open from top to bottom.

The life of the Jelly-fishes, with the exception of the Millepores and

the like, is short in comparison to that of other Radiates. While

Polyps live for many years, and Star-fishes and Sea-urchins require

ten or fifteen years to attain their full size, the short existence of

the Acaleph, with all its changes, is accomplished in one year. The

breeding season being in the autumn, the egg grows into a Hydroid

during the winter; in the spring the Jelly-fish is freed from the

Hydroid stock, or developed upon it as the case may be; it attains its

full size in the fall, lays its eggs and dies, and the cycle is

complete. The autumn storms make fearful havoc among them, swarms of

them being killed by the fall rains, after which they may be found

thrown up on the beaches in great numbers. When we consider the size

of these Jelly-fishes, their rapidity of growth seems very remarkable.

Our common Aurelia measures some twelve to eighteen inches in diameter

when full grown, and yet in the winter it is a Hydra so small as

almost to escape notice. Still more striking is the rapid increase of

our Cyanea, that giant among Jelly-fishes, which, were it not for the

soft, gelatinous consistency of its body, would be one of the most

formidable among our marine animals.

Before entering upon the descriptions of the special kinds of

Jelly-fishes, we would remind our readers that the radiate plan of

structure is reproduced in this class of animals as distinctly as in

the Polyps, though under a different aspect. Here also we find that

there is a central digestive cavity from which all the radiating

cavities, whether simple or ramified, diverge toward the periphery. It

is true that the open chambers of the Polyps are here transformed into

narrow tubes, by the thickening of the dividing partitions; or in

other words, the open spaces of the Polyps correspond to tubes in the

Acalephs, while the partitions in the Polyps correspond to the thick

masses of the body dividing the tubes in the Acalephs. But the

principle of radiation on which the whole branch of Radiates is

constructed controls the organization of Acalephs no less than that of

the other classes, so that a transverse section across any Polyp (Fig.

1), or across any Acaleph (Fig. 50), or across any Echinoderm (Fig.

140), shows their internal structure to be based upon a radiation of

all parts from the centre to the periphery.

That there may be no vagueness as to the terms used hereafter, we

would add one word respecting the nomenclature of this class, whose

aliases might baffle the sagacity of a police detective. The names

Acalephs, Medusæ, or the more common appellation of Jelly-fishes,

cover the same ground, and are applied indiscriminately to the animals

they represent. The name Jelly-fish is an inappropriate one, though

the gelatinous consistency of these animals is accurately enough

expressed by it; but they have no more structural relation to a fish

than to a bird or an insect. They have, however, received this name

before the structure of animals was understood, when all animals

inhabiting the waters were indiscriminately called fishes, and it is

now in such general use that it would be difficult to change it. The

name Medusa is derived from their long tentacular appendages,

sometimes wound up in a close coil, sometimes thrown out to a great

distance, sometimes but half unfolded, and aptly enough compared to

the snaky locks of Medusa. Their third and oldest appellation, that of

Acalephs,--alluding to their stinging or nettling property, and given

to them and like animals by Aristotle, in the first instance, but

afterwards applied by Cuvier in a more limited sense to

Jelly-fishes,--is the most generally accepted, and perhaps the most

appropriate of all.

The subject of nomenclature is not altogether so dry and arid as it

seems to many who do not fully understand the significance of

scientific names. Not only do they often express with terse precision

the character of the animal or plant they signify, but there is also

no little sentiment concealed under these jaw-breaking appellations.

As seafaring men call their vessels after friends or sweethearts, or

commemorate in this way some impressive event, or some object of their

reverence, so have naturalists, under their fabrication of appropriate

names, veiled many a graceful allusion, either to the great leaders of

our science, or to some more intimate personal affection. The _Linnæa

borealis_ was well named after his famous master, by a disciple of the

great Norwegian naturalist; _Goethea semperflorens_, the

ever-blooming, is another tribute of the same kind, while the pretty,

graceful little Lizzia, named by Forbes, is one instance among many of

a more affectionate reference to nearer friends. The allusions of this

kind are not always of so amiable a character, however,--witness the

"Buffonia," a low, noxious weed, growing in marshy places, and named

by Linnæus after Buffon, whom he bitterly hated. Indeed, there is a

world of meaning hidden under our zoölogical and botanical

nomenclature, known only to those who are intimately acquainted with

the annals of scientific life in its social as well as its

professional aspect.

* * * * *

CTENOPHORÆ.

The Ctenophoræ differ from other Jelly-fishes in their mode of

locomotion. All the Discophorous Medusæ, as well as Hydroids, move by

a rhythmical rise and fall of the disk, contracting and expanding with

alternations so regular, that it reminds one of the action of the

lungs, and seems at first sight to be a kind of respiration in which

water takes the place of air. The Greeks recognized this peculiar

character in their name, for they called them Sea-lungs. Indeed,

locomotion, respiration, and circulation are so intimately connected

in all these lower animals, that whatever promotes one of these

functions affects the other also, and though the immediate result of

the contraction and expansion of the disk seems to be to impel them

through the water, yet it is also connected with the introduction of

water into the body, which there becomes assimilated with the food in

the process of digestion, and is circulated throughout all its parts

by means of ramifying tubes. In the Ctenophoræ there is no such

regular expansion and contraction of the disk; they are at once

distinguished from the Discophoræ by the presence of external

locomotive appendages of a very peculiar character. They move by the

rapid flapping of countless little oars or paddles, arranged in

vertical rows along the surface of the disk, acting independently of

each other; one row, or even one paddle, moving singly, or all of them

together, at the will of the animal; thus enabling it to accelerate or

slacken its movements, to dart through the water rapidly, or to

diminish its speed by partly furling its little sails, or, spreading

them slightly, to poise itself with a faint, quivering movement that

reminds one of the pause of the humming-bird in the air,--something

that is neither positive motion, nor actual rest.[3]

[Footnote 3: The flappers of one side are sometimes in full

activity, while those of the other side are perfectly quiet or

nearly so, thus producing rotatory movements in every direction.]

These locomotive appendages are intimately connected with the

circulating tubes, as we shall see when we examine the structural

details of these animals, so that in them also breathing and moving

are in direct relation to each other. To those unaccustomed to the

comparison of functions in animals, the use of the word breathing, as

applied to the introduction of water into the body, may seem

inappropriate, but it is by the absorption of aerated water that these

lower animals receive that amount of oxygen into the system, as

necessary to the maintenance of life in them, as a greater supply is

to the higher animals. The name of Ctenophoræ or comb-bearers, is

derived from these rows of tiny paddles which have been called combs

by some naturalists, because they are set upon horizontal bands of

muscles, see Fig. 29, reminding one of the base of a comb, while the

fringes are compared to its teeth. These flappers add greatly to the

beauty of these animals, for a variety of brilliant hues is produced

along each row by the decomposition of the rays of light upon them

when in motion. They give off all the prismatic colors, and as the

combs are exceedingly small, so that at first sight one hardly

distinguishes them from the disk itself, the exquisite play of color,

rippling in regular lines over the surface of the animal, seems at

first to have no external cause.

_Pleurobrachia_. (_Pleurobrachia rhododactyla Ag_.)

[Illustration: Fig. 27. Pleurobrachia seen at right angles to the

plane in which the tentacles are placed. (_Agassiz_.)]

Among the most graceful and attractive of these animals are the

Pleurobrachia (Fig. 29), and, though not first in order, we will give

it the precedence in our description, because it will serve to

illustrate some features of the other two groups. The body of the

Pleurobrachia consists of a transparent sphere, varying, however, from

the perfect sphere in being somewhat oblong, and also by a slight

compression on two opposite sides (Figs. 27 and 28), so as to render

its horizontal diameter longer in one direction than in the other

(Fig. 30). This divergence from the globular form, so slight in

Pleurobrachia as to be hardly perceptible to the casual observer,

establishing two diameters of different lengths at right angles with

each other, is equally true of the other genera. It is interesting and

important, as showing the tendency in this highest group of Acalephs

to assume a bilateral character. This bilaterality becomes still more

marked in the highest class of Radiates, the Echinoderms. Such

structural tendencies in the lower animals, hinting at laws to be more

fully developed in the higher forms, are always significant, as

showing the intimate relation between all parts of the plan of

creation. This inequality of the diameters is connected with the

disposition of parts in the whole structure, the locomotive fringes

and the vertical tubes connected with them being arranged in sets of

four on either side of a plane passing through the longer diameter,

showing thus a tendency toward the establishment of a right and left

side of the body, instead of the perfectly equal disposition of parts

around a common centre, as in the lower Radiates.

[Illustration: Fig. 28. Pleurobrachia seen in plane of tentacles.

(_Agassiz_.)]

The Pleurobrachia are so transparent, that, with some preparatory

explanation of their structure, the most unscientific observer may

trace the relation of parts in them. At one end of the sphere is the

transverse split (Fig. 27), that serves them as a mouth; at the

opposite pole is a small circumscribed area, in the centre of which is

a dark eye-speck. The eight rows of locomotive fringes run from pole

to pole, dividing the whole surface of the body like the ribs on a

melon. (Figs. 27, 28.) Hanging from either side of the body, a little

above the area in which the eye-speck is placed, are two most

extraordinary appendages in the shape of long tentacles, possessing

such wonderful power of extension and contraction that, while at one

moment they may be knotted into a little compact mass no bigger than a

pin's head, drawn up close against the side of the body, or hidden

within it, the next instant they may be floating behind it in various

positions to a distance of half a yard and more, putting out at the

same time soft plumy fringes (Fig. 29) along one side, like the beard

of a feather. One who has never seen these animals may well be

pardoned for doubting even the most literal and matter-of-fact account

of these singular tentacles. There is no variety of curve or spiral

that does not seem to be represented in their evolutions. Sometimes

they unfold gradually, creeping out softly and slowly from a state of

contraction, or again the little ball, hardly perceptible against the

side of the body, drops suddenly to the bottom of the tank in which

the animal floating, and one thinks for a moment, so slight is the

thread-like attachment, that it has actually fallen from the body; but

watch a little longer, and all the filaments spread out along the side

of the thread, it expands to its full length and breadth, and resumes

all its graceful evolutions.

[Illustration: Fig. 29. Natural attitude of Pleurobrachia when in

motion.]

[Illustration: Fig. 30. Pleurobrachia seen from the extremity

opposite the mouth.]

One word of the internal structure of these animals, to explain its

relation to the external appendages. The mouth opens into a wide

digestive cavity (Figs. 27, 28), enclosed between two vertical tubes.

Toward the opposite end of the body these tubes terminate or unite in

a single funnel-like canal, which is a reservoir as it were for the

circulating fluid poured into it through an opening in the bottom of

the digestive cavity. The food in the digestive cavity becomes

liquefied by mingling with the water entering with it at the mouth,

and, thus prepared, it passes into this canal, from which, as we shall

presently see, all the circulating tubes ramifying throughout the body

are fed. Two of these circulating tubes, or, as they are called from

the nature of the liquid they contain, chymiferous tubes, are very

large, starting horizontally and at right angles with the digestive

cavity from the point of junction between the vertical tubes (Fig. 30)

and the canal. Presently they give off two branches, those again

ramifying in two directions as they approach the periphery, so that

each one of the first main tubes has multiplied to four, before its

ramifications reach the surface, thus making in all eight radiating

tubes. So far, these eight tubes are horizontal, all diverging on the

same level; but as they reach the periphery each one gives rise to a

vertical tube, running along the surface of the body from pole to

pole, just within the rows of locomotive fringes on the outer surface,

and immediately connected with them (Figs. 27, 28). As in all the

Ctenophoræ, these fringes keep up a constant play of color by their

rapid vibrations. In Pleurobrachia the prevailing tint is a yellowish

pink, though it varies to green, red, and purple, with the changing

motions of the animal. We have seen that the vertical tubes between

which the digestive cavity is enclosed, start like the cavity itself

from that pole of the body where the mouth is placed, and that, as

they approach the opposite pole, at a distance from the mouth of about

two thirds the whole length of the body, they unite in the canal,

which then extends to the other pole where the eye-speck is placed. As

it is just at this point of juncture between the tubes and the canal

that the two main horizontal tubes arise from which all the others

branch on the same plane (Figs. 27, 28), it follows that they reach

the periphery, not on a level with the pole opposite the mouth, but

removed from it by about one third the height of the body. In

consequence of this the eight vertical tubes arising from the

horizontal ones, in order to run the entire length of the body from

pole to pole, extend in opposite directions, sending a branch to each

pole, though the branch running toward the mouth is of course the

longer of the two. The tentacles have their roots in two sacs within

the body, placed at right angles with the split of the mouth. (Figs.

27, 30.) They open at the surface on the opposite side from the mouth,

though not immediately within the area at which the eye-speck is

placed, but somewhat above it, and at a little distance on either side

of it. The tentacles may be drawn completely within these sacs, or be

extended outside, as we have seen, to a greater or less degree, and in

every variety of curve or spiral.

_Bolina_. (_Bolina alata_ AG.)

[Illustration: Fig. 31. Bolina seen from the broad side; _o_

eye-speck, _m_ mouth, _r_ auricles, _v_ digestive cavity, _g_ _h_

short rows of flappers, _a_ _f_ long rows of flappers, _n_ _x_ _t_

_z_ tubes winding in the larger lobes; about half natural size.

(_Agassiz_.)]

[Illustration: Fig. 32. Bolina seen from the narrow side; _c_ _h_

short rows of flappers, _a_ _b_ long rows of flappers; other

letters as in Fig. 31. (_Agassiz_.)]

Seaside Studies in Natural History. Marine Animals of Massachusetts Bay. Radiates. · 第 2 / 11 段