As the spicules of sponges are in themselves beautiful objects, and are important to the naturalist, inasmuch as they form a basis for the classification of sponges, it is well to know by what means they may be separated from the animal for microscopic examination. The separation is based on the fact that nitric acid (aqua-fortis) will destroy organic matter while it has not the slightest action on silica. In some of our common horny sponges the fibres are so transparent that, when teased out and placed under the microscope, the siliceous spicules may be seen embedded within them, but the spicules, both in these and the fleshy sponges, may be separated completely from the animal matter by putting a fragment of the sponge in a test-tube, covering it with nitric acid, and boiling it for a short time. The tube should then be filled up with water and allowed to stand undisturbed for a time, after which the liquid is poured off gently from the sediment. If the sediment is then put under the microscope on a slip of glass, it will be seen to consist of grains of sand, of which there is always a considerable amount in the pores and cavities of a sponge, and the siliceous spicules.
Among the common objects of the sea shore is the horny skeleton of the sponge Chalina oculata, which is frequently washed on the beach by the waves, especially after storms. This sponge is not likely to be seen between the tide-marks except at the lowest spring tide, when it may be found suspended in a sheltered crevice or cave. The skeleton consists of a fine network of horny fibres, in the centre of which lie the spicules, imbedded in the horny material. The spicules are short and straight, tapering at both ends.
The Bread-crumb sponge (Halichondria panicea) is even more common, for it is to be found on every rocky coast, encrusting weeds and rocks, often considerably above low-water mark. It is of a yellowish or pale greenish colour, and forms an incrustation varying in thickness from one-twentieth of an inch to half an inch or more; and, like most sponges, should be looked for in narrow crevices, under heavy growths of weeds, or in other situations where it is protected from the light. Sometimes its free surface is unbroken, except, of course, by the minute pores, and, here and there, the larger openings that serve for the outgoing currents; but when it is found encrusting a rock in patches of considerable size, the larger holes all occupy the summit of a little cone resembling a miniature volcano with its crater. This sponge is easily removed from the rock with the aid of a blunt broad-bladed knife, and retains its natural appearance to perfection if preserved in methylated spirit. Its horny skeleton is of a very compact nature, and the spicules are minute siliceous needles pointed at both ends.
Rambling on the sea beach we frequently meet with old oyster and other shells perforated by a number of circular holes about the size of a pin’s head or less, and chalk and limestone rocks also are seen similarly bored. On breaking into or grinding down the substance we find that the openings are the ends of channels that form a network of canals and chambers, some of which are so near the surface that they are covered by an exceedingly thin layer of the calcareous substance. These canals and chambers form the home of the Boring Sponge (Cliona), which, although a very soft-bodied animal, has itself excavated them.
The manner in which the Cliona excavates such a complicated system of passages in so hard a material has naturally raised a considerable amount of curiosity, and those who have studied the matter are divided in opinion as to whether the work is done by chemical or by mechanical action.
Some of those who advocate the chemical theory suppose that an acid fluid is secreted by the sponge, and that the carbonate of lime forming the shell or stone is thereby dissolved; but such advocates have, as yet, failed to detect the presence of any acid substance in the body of the animal. Others ascribe the action to the solvent power of carbonic acid gas. This gas certainly has the power of dissolving carbonate of lime, as may be proved by a very simple experiment: Pour a little lime water into a glass, and blow into it through a glass tube. The lime water speedily becomes milky in appearance, the lime having been converted into particles of chalk or carbonate of lime by union with the carbonic acid gas from the lungs. Continue to blow into the liquid for some time, and the carbonate of lime will slowly disappear, being gradually dissolved by the excess of the gas—the gas over and above that required for the formation of the carbonate. Thus, it has been said, the carbonic acid gas evolved as a product of the respiration of the sponge is the agent by which the channels are excavated. Whatever be the acid to which this power is ascribed, whether it be the carbonic acid or a special acid fluid secreted for the purpose, there is still this difficulty in the way of accepting the theory, namely, that an acid, though it has the power of dissolving the mineral matter of a shell—the carbonate of lime—has no action on the laminæ of animal substance that form part of the structure. If we put the shell of a mollusc in hydrochloric or dilute nitric acid, we obtain, after the complete solution of the carbonate of lime, a substantial residue of animal matter which the acid does not touch, but in the case of Cliona both animal and mineral substances yield to its power.
Those who favour the mechanical theory assert that the material is worn away by siliceous particles developed by the sponge, and kept in constant motion as long as the animal lives; and the theory is supported by the statement that, in addition to the spicules of silica, which are pin-shaped, and occupy the interior of the animal, there are little siliceous granules scattered on the surface of the sponge which are kept in constant motion resembling that of cilia; and the minute particles of carbonate of lime that form a dusty deposit within the galleries are supposed to be the product of the rasping or drilling action of these granules.
The pin-shaped spicules of Cliona may be obtained for microscopic examination by breaking any old oyster shell that has formed its home, and brushing out the dust from the galleries; or, a part of the shell may be dissolved in acid, and the sediment examined for spicules on a slip of glass.
One of the most interesting groups of marine life is that including jelly-fishes and anemones. In it are the pretty little sea firs, so often mistaken for sea-weeds by the youthful admirers of these plants, who almost always include them in their collection of marine algæ; the transparent, bell-shaped jelly-fishes, which may often be seen in thousands during the summer, carried by the tides, and swimming gently by graceful contractions of their bells; and, most beautiful of all, the lovely anemones—the ‘sea flowers’ of the older naturalists, by whom they were regarded as forms of vegetable life.
The simplest animals of this group are minute jelly-like creatures, of a more or less cylindrical form, usually fixed at one end, and having a mouth at the other. The body is a simple hollow cylinder, the wall of which is made up of two distinct layers, while the cavity within serves the purpose of a stomach. The mouth is surrounded by a circle of arms or tentacles by means of which the creature is enabled to capture its prey. These arms are capable of free movement in every direction, and can be readily retracted when the animal is disturbed. They are also armed with minute oval, hollow cells, each of which has a slender filament coiled up into a spiral within its cavity. Each filament is capable of being suddenly protruded, thus becoming a free whip-like appendage, and these are so numerous as to be very effectual in seizing and holding the living beings on which the animal feeds. This would undoubtedly be the case even if they were capable of mechanical action only, but, in many instances at least, they seem to be aided by the presence of some violent irritant, judging from the rapidity with which the struggling prey is paralysed when seized, especially in the case of some of the larger members of the group.
The simple forms referred to increase by a process of budding, the buds appearing first as simple swellings on the side of the parent creature, and afterwards developing a mouth and tentacles, thus becoming exactly like the adult form. Clusters of eggs also are developed in the outer layer of the body-wall, and these are set free at intervals, and produce new individuals. These animals possess no blood system of any kind, and have no special organs for respiration, but the nutrient matter absorbed from the body-cavity permeates the soft structures of the flower-like body, and the oxygen required for respiratory purposes is readily absorbed from the surrounding water.
The higher cœlenterates differ in certain particulars from the lower forms just referred to. Thus, they frequently have a large number of tentacles around the mouth, often arranged in several distinct whorls. They have also a stomach separate from the general body-cavity, but communicating with the latter below; and the body-cavity is divided into compartments by a number of radiating partitions. Some, also, develop a hard, stony skeleton by secreting carbonate of lime obtained from the water in which they live.
We often see, when collecting on the beaches of rocky coasts, and especially after storms, a number of vegetable-like growths, of a greyish or brownish colour, each consisting of one or more main stalks bearing a number of delicate branches. Some of them, by their peculiar mode of growth, have suggested the name of sea firs, and a few of these, together with other animals of the same group, may readily be recognised by the accompanying illustrations. They are the objects already referred to as being commonly included in collections of sea-weeds by young naturalists, but they are in reality the horny skeletons of colonies of cœlenterates of the simplest type, belonging to the division Hydrozoa.
If we examine them with a lens we find that there are little cup-like bodies projecting from each portion or branch of the stem-like structure, and that the stem itself is hollow, with a communicating pore at the base of each cup. This constitutes the skeleton only of the colony—the dead matter, so to speak, which persists after the living creatures have perished; but if the specimens collected have been obtained fresh from the sea, placed in a glass of sea water, and then examined with the aid of a lens, little jelly-like hydroids or polypites will be seen to protrude from the cups, and extend their short arms in search of food.
Each of the little creatures has a tubular stalk which passes through the hole at the base of the cup, and is continuous with a tube of gelatinous material in the interior of the horny stem, and thus each member of the colony is directly connected with all the others, so that any nutrient matter collected and digested by one member may be absorbed into the central tube for the nourishment of the entire company of little socialists, the activity of the one being thus made to compensate for the laziness or incompetency of others. And this provision seems to be absolutely necessary for the well-being of the colony as a whole, for a close examination will often show that a kind of division of labour has been established, since it includes two or three distinct kinds of polypites, each adapted for the performance of a certain function. Thus, in addition to the feeding or nutritive members of the community, there are some mouthless individuals whose sole function seems to be the production of eggs for the propagation of the species, while others, also mouthless, develop an enormous number of stinging cells, probably for the protection of the whole community against its enemies, and these must therefore be provided, as we have seen they are, with a means by which they may derive nourishment through the agency of the feeding polypites.
When the eggs are liberated from what we may call the reproductive members, they are carried away by the currents or tides, and soon develop into little larvæ which are very unlike the parent, since they are covered with minute vibratile cilia by means of which they can swim freely. This they do for a period, and then settle down, lose their cilia, become stalked, and thus constitute the foundation of a new colony. A tubular stalk grows upward from its root, new members are added as outgrowths or buds from their progenitor, and so the growth proceeds until an extensive colony of hundreds of individuals has been formed.
We have spoken of the hydroid communities as being washed up on the beaches of our rocky coasts, but the collector of these interesting objects should not depend on such specimens for purposes of study. It is undoubtedly true that splendid examples of the sea firs and their allies are frequently washed up by the waves, including some species that inhabit deep water, and which are, consequently, not to be found by the ordinary collector in their proper habitat, and that these may often be secured with the polypites still alive; but several species are to be obtained between the tide-marks, especially at extreme low water, growing on rocks, weeds, and shells; and we have often met with good specimens, still alive, attached to the shells of whelks, scallops, &c., in fishmongers’ stores, even in inland towns.
Sometimes individual polypites become detached from a colony, and develop into little umbrella-shaped jelly-fishes, about a fifth of an inch in diameter; and these float about freely, keeping themselves near the surface by rhythmic contractions of their ‘bells,’ the margins of which are fringed by numerous fine tentacles. The mouth is situated centrally on the under side, and is surrounded by a circular canal from which proceed radiating tubes; and pigmented spots, supposed to be rudimentary eyes, are formed round the edge. These little bodies are called Medusoids, and may frequently be seen floating round our coasts towards the end of the summer. In the water they are almost invisible on account of the extreme transparency of their bodies; but if a muslin net be drawn through the water from the stern of a boat, and the net then gently turned inside out in a vessel of sea water, a number of medusoids may be obtained for examination. These creatures produce eggs which yield small ciliated larvæ that swim about freely for a time, and then settle down and establish stalked colonies as previously described.
The larger jelly-fishes or Medusæ so frequently seen floating in enormous numbers near the surface of the sea during the summer months are allied to the medusoids. Their bodies are so soft that it is a difficult matter to remove them from the water without injury, and when removed their graceful forms are completely destroyed by the pressure of their own weight. When left stranded on the beach, as is often the case, they seem to dissolve almost completely away, so readily does the soft animal tissue disintegrate in the large proportion of water, which forms about 95 per cent. of the weight of the whole body.
Those who desire to examine the nature and movements of the medusæ will find it necessary to observe them in water. The creatures may be lifted out of the sea in a vessel placed below them, and then transferred to a glass tank or a still rock pool by submerging the vessel and allowing them to float out. It will then be observed that the mouth is situated at the summit of a tube that projects from the middle of the under side of the ‘bell,’ and is surrounded by lobed or frilled lips. Marginal tentacles also generally fringe the edge of the bell, projecting downwards into the water. Round the circumference of the body may be seen a circular canal, from which several tubes converge towards, and communicate with, the cavity of the stomach.
When a medusa is inactive, its body gradually sinks to the bottom, being usually slightly heavier than the water in which it lives; but it is enabled to keep afloat by those rhythmic contractions of the bell with which we are so familiar. It seems that the medusæ are very sensitive to various external conditions, for they frequently disappear simultaneously from the surface water, and as suddenly reappear in shoals when the conditions are more favourable; but it is difficult to understand the causes which give rise to these remarkable movements.
The medusæ are often termed the Acalephæ—a word which signifies ‘nettles,’ and they are popularly known as sea nettles. They all possess stinging cells, which are distributed most thickly in the tentacles, and some of the larger species are undoubtedly able to produce an impression on the bodies of unwary bathers, while almost all have the power of paralysing the living prey on which they feed.
By far the commonest of the jelly-fishes of our seas is the beautiful blue medusa—Aurelia aurita. This species appears in enormous shoals during the summer, and large numbers are washed upon flat, sandy beaches. They vary in size from two or three inches to nearly a foot in diameter, and may be recognised from our illustration. The ‘bell’ is umbrella-shaped, and is so transparent that the stomach with its radiating canals may be seen through its substance. Around the margin there are little pigment spots which are supposed to be rudimentary eyes, and little cavities, containing a clear fluid, that are thought to serve the purpose of ears.
On the under surface may be seen the square mouth, furnished with four long and graceful frilled lips, which are richly supplied with stinging cells; also the four ovaries or egg-producing organs, rendered conspicuous by their violet colouring.
The life history of Aurelia is most interesting. The eggs are produced in pouches that communicate directly with the stomach-cavity, and these give rise to little ciliated larvæ that are ejected through the mouth, and then swim about freely in the water for a time. After this they settle at the bottom, lose their cilia, and become little cylindrical jelly-fishes, fixed by a short stalk-like foot to rocks or weeds Numerous tentacles develop as the creatures increase in size, and a number of transverse furrows appear at the surface. The furrows gradually increase in depth until, at last, the body is broken up into several star-like discs, each of which floats away and develops into a new medusa.
Other jelly-fishes, some of which are considerably larger than Aurelia, frequent our seas, and are often to be seen stranded on the beach. Two of these—Rhizostoma and Chrysaora—are figured. Although they differ considerably in form from the blue aurelia, they closely resemble it in general structure and habits.
When strolling on flat, sandy beaches, especially in the spring and early summer, we commonly see what appear to be little balls of exceedingly transparent and glassy jelly, no larger than an ordinary marble. If picked up and examined, we observe that they are not quite spherical, but oval in form, with a little tubercle at one end, and eight equidistant bands running from this to the opposite end, like the meridians on a globe.
This extremely beautiful little creature is one of the cœlenterates, belonging to the division Ctenophora, or comb-bearing jelly-fishes, so called because they possess comb-like ciliated plates, and is called the Globular Beroe (Cydippe pileus).
The ctenophores are very active creatures, swimming freely in the open seas by means of their numerous cilia; and, although of such delicate structure, are very predaceous, devouring small crustaceans and other marine animals. They are usually globular in form, but some are like long ribbons, and almost all are remarkable for their wonderful transparency, which renders them nearly invisible when floating in water. They have not the power of stinging or paralysing their prey, as the medusæ have, but their fringed arms are provided with adhesive cells by which they hold their prey tenaciously.
In order to observe the form and habits of the Beroe we transfer it to a vessel of sea water, when it immediately displays its regular spheroid form, and its eight rows of comb-like plates which form the meridians before alluded to. Its mouth is situated on the little tubercle at what we may call the lower pole, for it is the habit of the Beroe to swim in an inverted position, and the digestive cavity may be seen through its glassy body.
At first no appendages of any kind are visible, but soon the animal protrudes two long and exceedingly slender arms, fringed with slender gelatinous threads, from two cavities, at opposite sides of the body, into which they can be withdrawn. A close examination will also reveal the rapid movements of the cilia of its combs, and it is remarkable that these do not always work together, the animal being able to move any of its plates independently, and to reverse their motion when occasion requires. It has no tentacles corresponding with those of jelly-fishes and anemones, but is assisted in the capture of its prey by its two long arms, the chief use of which, however, seems to be that of a rudder for steering.
If the Beroe is left out of water for some time, the water which forms such a large proportion of its body evaporates, leaving an almost imperceptible residue of solid matter; and if left in water after it is dead, its substance rapidly dissolves away, leaving not the slightest trace of its presence. There seems to be no satisfactory way of preserving this beautiful form of animal life. If placed in strong spirit the water is rapidly extracted from its body, and its animal substance shrivelled to a minute, shapeless mass; while in weak spirit and in other fluid preservatives it becomes more or less distorted, and deprived of its beautiful transparency, or else it disappears altogether.
We now come to the great favourites among the cœlenterates—the beautiful anemones-the animated flowers of the ocean, remarkable not only for their lovely flower-like forms, but also for the great variety of colour and of habits which they display. These, together with the corals, form the division of the cœlenterates known as the Zoantharia, characterised by the possession of simple tentacles, the number of which is a multiple of either five or six. The latter differ from the former mainly in the power of secreting a calcareous skeleton which remains attached by its base after the animal substance has decayed.
The expanded anemone exhibits a more or less cylindrical body, attached by a suctorial base to a rock or some other object, and a broad circular disc above. In the centre of this disc is the mouth, surrounded by the tentacles, often very numerous, and arranged in one or more whorls. When the animal is inactive the tentacles are usually completely withdrawn, and the body contracted into a semiglobular or pear-shaped mass which is very firm to the touch.
The general internal structure of an anemone may be made out by simple dissections, and the examination conducted with the specimen submerged in water. A longitudinal section will show that the body is a double tube, the outer being formed by the body-wall, and the inner by the wall of the stomach. Thus there is a body-cavity distinct from that of the stomach, but the two will be seen to communicate below, since the stomach-wall does not extend as far down as the base. It will be seen, too, that the body-wall is made up of two distinct layers—an outer one, that is continued inward at the mouth to form the inner wall of the stomach, and an inner one that lines the whole of the body-cavity. The latter contains the muscular elements that enable the anemone to contract its body.
When the animal is expanded, the whole interior is filled with sea water, as are also the tentacles, which are hollow tubes, really extensions of the body-cavity, and formed by prolongations of the same two layers that constitute the body-wall. As it contracts this water is expelled, partly through the mouth, and partly through small openings that exist at the tips of the tentacles.
Fig. 90.—Section of an Anemone
t, tentacles; m, mouth; s, stomach; b c, body-cavity p, mesentery; o, egg-producing organ
The outer layer of the body-wall is provided with stinging cells which serve not only to protect the anemone from its enemies, but also to aid it in the capture of its prey, for which latter purpose they are distributed in much greater abundance in the tentacles.
The body-cavity is divided into a number of communicating compartments by means of vertical partitions running from the body-wall and converging towards the centre of the cavity. These are called mesenteries, and are extensions of the inner layer of the body-wall. Five or six of these are larger than the others, extending from disc to base, and are called primary mesenteries. Between these are an equal number of smaller secondary mesenteries; and, sometimes, a third set of still smaller tertiary mesenteries.
These internal partitions are best displayed in a transverse section of the body, which shows the double tube formed by the walls of the body and the stomach, together with the wheel-like arrangement of the mesenteries. At one time all animals that had a radial symmetry—the regular arrangement of parts round a common centre—were grouped together under the title of Radiata; but it has since been recognised that the creatures of this group exhibited such a great diversity of structure that they have been re-classified into two main divisions, one of which constitutes the cœlenterates which we are at present considering, and the other containing such creatures as star fishes and sea urchins.
On the surface of the mesenteries of the anemone may be seen the ovaries or egg-producing organs. These discharge the ova into the general body-cavity, after which they are ejected through the mouth. The embryos are minute jelly-like creatures that have an active existence, swimming about freely in the ocean by means of vibrating cilia, but after this period of activity they settle down and fix themselves, gradually assuming the adult form common to the species.
The habits of sea anemones are particularly interesting, and it will well repay anyone to make a study of these animals in their natural haunts as well as in the aquarium. The gentle swinging of the tentacles when searching for food, the capture and disposal of the prey, the peculiar modes of locomotion, and the development of the young, are among the chief points of interest. As regards locomotion, the usual method of moving from place to place is by an exceedingly slow gliding of the base or ‘foot’; and while some anemones are almost constantly on the move, others hardly ever stir from the secluded niche in which they have taken up their abode.
Sometimes an anemone will detach itself from the rock, and drag itself along, but very slowly, by means of its tentacles, sometimes inverting its body and walking on its head, as it were, and though one may never have the opportunity of witnessing this manœuvre on the shore, we have found it far from an uncommon occurrence in the aquarium.
The natural food of anemones consists of small crustaceans, such as shrimps, and crabs, molluscs, small fishes, and in fact almost every kind of animal diet, and there need never be any difficulty in finding suitable viands for species kept in captivity. It is really astonishing to see what large morsels they can dispose of with the assistance of their extensile mouths and stomachs. It is not even necessary, indeed, that the morsel be so small as to be entirely enclosed by the walls of its digestive cavity, for the anemone will digest one portion while the other remains projecting beyond its mouth. Further, it will even attack bodies which it cannot swallow at all, by protruding its stomach so as to partially envelope them, and then digesting the portion enclosed. Indigestible portions of its food, such as the shells of small molluscs, are ejected through the mouth after the process of digestion has been completed.
We have already referred to the reproduction of sea anemones by means of eggs, but it is interesting to note that they may also increase by a division of the body into two or more parts, and that this division may be either natural or artificial.
If an anemone be cut into halves longitudinally, each half will develop into a complete animal. If cut transversely, the upper portion will almost always develop a new suctorial disc, and produce a new individual complete in every respect; and it has been stated that the basal portion of the divided animal will also, occasionally, produce a new disc and tentacles.
The natural division of the anemone has frequently been spoken of as by no means an uncommon occurrence, but, as far as our experience of captive anemones go, this mode of multiplication does not seem to take place except as the result of some mechanical force applied, or as a means by which the animal may relieve itself of a solid body that it is unable to eject. Thus, on one occasion, when a stone had slipped so that its narrow edge rested across the middle of the disc of a large Mesembryanthemum, the animal, apparently unable to free itself from the burden, simply withdrew its tentacles and awaited results. In a few days two individuals were to be seen, one on either side of the stone, both undoubtedly produced as the result of the pressure applied. This instance seems to be exactly akin to artificial division, for it is far more likely that the animal was severed by the simple pressure of the stone than that it divided itself to be relieved of its burden.
On another occasion an anemone that had almost entirely surrounded a mussel on which it had been feeding, gradually released itself of the shell by a longitudinal division of its body; but here, again, it is probable that the fission was the result of pressure applied rather than of any power on the part of the animal.
A few of the British sea anemones are shown on Plates II. and III., and although the coloured illustrations will probably suffice for purposes of identification, yet a short description of each one represented may be acceptable.
The most common and most widely distributed species is undoubtedly the familiar Beadlet (Actinia mesembryanthemum—Plate II., figs. 1, 2, 3), which is to be found on every bit of rocky coast around the British Isles, and even on some stony beaches where there are no standing rocks between the tide-marks.
The colour of this species is exceedingly variable, but the most abundant variety is of a liver-brown colour, with crimson disc and tentacles, brilliant blue spots round the margin of the disc, and a line of bright blue around the base. In others the prevailing colour is deep crimson, orange, yellowish brown, or green. Fig. 1 represents a variety commonly known as the Strawberry Beadlet (Fragacea), which is distinguished by its superior size, and in which the dark-red ground is often conspicuously spotted with green.
Two members of the same genus are also shown on Plate III. One of these—A. glauca (fig. 3)—is of a bluish-green colour; while the other—A. chiococca (fig. 4)—is bright scarlet, with deep crimson disc and white spots round the disc.
Plate II
SEA ANEMONES
| 1, 2, 3, Actinia mesembryanthemum. | 6. Sagartia bellis. |
| 4. Caryophyllia Smithii. | 7. Balanophyllia regia. |
| 5. Tealia crassicornis. | 8. Actinoloba dianthus. |
The general form of this genus is that of an expanded flower on a short column; the name Beadlet is applied on account of the little bead-like projections on the margin of the disc. The tentacles number nearly two hundred in a fully grown individual, and are arranged in several rows; but when the animal is disturbed and the tentacles retracted, its form is almost hemispherical.
It is interesting to note that A. mesembryanthemum not only exists in varieties distinguished by distinct colours, but that the same individual will sometimes change its tint, as may be observed when it is kept in the aquarium; and it may be mentioned, by the way, that it is very easily reared in captivity, either in the natural or the artificial salt water, for not only may the same individuals be kept alive for years with only a moderate amount of attention, but their offspring may be reared without difficulty.
On Plate II. (fig. 8) are two illustrations of the beautiful Actinoloba dianthus, which grows to a length of five or six inches, and is easily distinguished by its expanded and frilled disc, its very numerous short and slender tentacles, and its tall, pillar-like body. Its colour is somewhat variable, being either salmon, flesh-colour, cream, white, red, orange, or brownish; but whatever be the tint of the body and tentacles, the margin of the mouth is always red or orange. When young it may easily be mistaken for another species, as its disc is not then frilled, and the tentacles are much fewer in number.
This pretty anemone usually inhabits deep water, and is frequently brought in, attached to shells and stones, by trawlers, but it may be commonly observed in the dark crevices of rocks, a little above low-water mark, where it is usually seen contracted into a ball, or even so much flattened that it looks like a mere pulpy incrustation of the rock. It is very common on the rocky coasts of Dorset, Devon, and Cornwall, as well as in many parts of Scotland and Ireland.
Like the Beadlet, it is easily kept alive in the aquarium, where it commonly multiplies by natural division; but as it does not generally expand in full daylight, its beauty is often better observed at night by artificial light.
On Plate II. (fig. 5) we have an illustration of the beautiful Dahlia Wartlet (Tealia crassicornis), which may be readily recognised by its thick, banded, horn-like tentacles, and the numerous little adhesive warts that almost cover the surface of its body.
This species is as abundant as it is beautiful, for it is to be found in plenty on almost every rocky coast, where it may be seen in the rock pools and in the crevices of rocks near low-water mark. The diameter of its cylindrical body often reaches two or three inches, while the expanded tentacles embrace a circle of four or five inches. Specimens even much larger than this are sometimes obtained by dredging in deep water.
The ‘Dahlia’ is not so frequently seen by sea-side collectors as its abundance would lead one to expect, and this is principally due to the fact that it not only conceals itself in narrow and out-of-the-way crevices and angles of rocks, but also that, on the retreat of the tide, it generally covers itself with small stones, fragments of shells, &c., held fast to its body by means of its numerous suckers. In this manner it conceals its beauty so well that the sense of of sight, is necessary in determining its whereabouts. As a rule, however, it does not resort to this method of concealment when it inhabits deep water, or even a permanent rock pool between the tide-marks, and thus it is in the latter home where one may expect to see this sea flower in all its glory, for when permanently covered with water it will seldom hide its crown, except when alarmed, or when in the act of swallowing its food.
It should be noted, too, that the rock pool is the right place in which to study the habits of this anemone, for it is not nearly so easy to rear in the artificial aquarium as the species previously described, and, moreover, it requires a great deal of food. We have found it live longest in running water, kept cool, and frequently renewed by supplies fresh from the sea. It may be fed on almost any, if not every, form of animal life inhabiting a rock pool. A small fish or a prawn is perfectly helpless when once it is seized by the creature’s tentacles. Mussels, winkles, limpets, &c., are eagerly swallowed, and the indigestible shells disgorged after the animal substance has been dissolved by the digestive fluid. Even the active shore crab, armed as it is with a coat of mail and powerful pincers, is no match for its powerfully adhesive tentacles; nor do the sharp spines of the prickly urchin preserve it from so voracious a creature.
The rocky coasts of Devon and Cornwall are the chief haunts of the pretty ‘Daisy Anemone’ (Sagartia bellis), and here it is very abundant in places. This species lives in holes and crevices of the rocks, its body usually entirely hidden from view, but its dark brown disc, intersected by bright red radiating lines, and fringed with numerous small tentacles, fully exposed to view as long as it is submerged. The length of its body is always adapted to the depth of the hole or crevice in which the animal lives, and may vary from half an inch to two or three inches, the diameter of the columns being greatest where the length is least.
Sometimes the ‘Daisy’ may be seen living a solitary life, having settled down in a hole just large enough to accommodate it, but more commonly it is seen in company with several others of its species, occupying a crevice in a rock pool, and often so closely packed together that the tentacles of each individual are intermingled with those of its neighbours, thus exhibiting a more or less continuous cluster or line of ‘flowers,’ each disc being from one to two or three inches in diameter when fully expanded.
On account of the peculiar positions selected by this species, it is not easily removed without injury, and hammer and chisel are almost always necessary for its removal; but if it is obtained without injury, and transferred to the indoor aquarium, but little difficulty will be found in keeping it alive and in health. It is also very prolific, and a single specimen placed in the indoor tank will frequently produce a large number of young.
The colour of S. bellis, like that of many of our anemones, is very variable, but the species may easily be recognised by the radiating lines of the disc, and the numerous small tentacles. One variety, however, deviates considerably in form, colour, and habit from the normal. It (Plate II., fig. 6) is of a dull yellow colour, and has a much less graceful form; and, instead of living in the holes and crevices of rocky coasts, where it would be washed by fresh sea water at every tide, it inhabits the muddy and fœtid waters of narrow inlets of the sea in the neighbourhood of Weymouth.