the property upon which the economic value of the bath sponge
depends. In the living sponge the fibres are embedded in the
mesogloea, where they are secreted by special cells known as
spongoblasts, which are often found thickly clustering around them
(fig. 7) The canal-system (figs. 6, 8) is very complex and shows
but little indication of its origin from a folded rhagon. The
inhalant pores lead each into a short, narrow, inhalant canal; these
unite in roomy subdermal cavities lying in the ectosome, and from
these in turn the main inhalant canals come off. The latter divide
and subdivide, and thus ramify
through the deeper parts of the
sponge amongst the flagellated
chambers, to each of which a small
number of slender canaliculi are
ultimately given off (fig. 9). The
chambers themselves, lined by the
usual collared cells, are small and
approximately spherical, and each
one discharges its water through a
short and narrow exhalant canaliculus
(fig. 9). The openings of
the inhalant canaliculi into the
chambers, of which there are several,
correspond to the prosopyles of an
Olynthus, while the single exhalant
opening, or apopyle, may possibly
correspond to an Olynthus osculum.
The exhalant canaliculi unite
together to form larger and larger
canals which finally lead the stream
of water to the vents on the surface
of the sponge (fig. 8). The various
parts of the canal-system, other
than the chambers themselves, are
lined by a flat pavement-epithelium,
and the mesogloea, occupying all
the spaces between the different
parts of the canal-system, contains
cells of various kinds, embedded in a very granular matrix.
Comparative Anatomy.
(After Ridley and Dendy. From a plate in “Challenger” Reports, xx., by permission of the Controller of H.M. Stationery Office.) |
Fig. 10.—Esperiopsis challengeri: a deep-water Monaxonellid Sponge. |
External Characters.—Amongst the simpler calcareous sponges which are all of comparatively small size, the external form is usually symmetrical and is evidently a kind of outward expression of the arrangement of the canal-system. This is well seen in the simplest form of all, the sac-shaped Olynthus, and also in its simpler Syconoid and Leuconoid derivatives (described later on), which may be regarded either as individuals of a higher order or as colonies of Olynthus persons grouped around a central individual whose large gastral cavity opens to the exterior through the single osculum. In the more complex Leuconoids, however, the process of colony formation becomes very irregular and may give rise to great compound masses, with many vents. In these masses we may perhaps recognize the presence of individuals of three orders: (1) the primitive Olynthus persons, represented by the individual flagellated chambers; (2) the Leuconoid persons, indicated each by its osculum; and (3) the entire colony formed by the union of many such Leuconoid persons in an irregular manner. It is, however, very doubtful how far the flagellated chambers in such forms as this can be regarded as morphologically equivalent to Olynthus persons.
In the non-calcareous sponges we are always dealing with individuals of a high order, which usually form complex aggregates (colonies) of large size and very various shape. As a general rule the form of those non-calcareous sponges which grow in shallow water is extremely irregular and variable while at great ocean depths the shape is usually definite, constant and often exquisitely symmetrical, a fact which may perhaps be accounted for in part by the absence of disturbing influences such as are met with in shallow water. Perhaps the most extraordinary external form yet discovered is that of Esperiopsis challengeri, discovered by the “Challenger” expedition in deep water off the Philippine Islands (fig. 10), a form which reminds one strikingly of a number of flowers arranged in a raceme, except that the largest and oldest member of the compound colony is at the top of the stalk and the smallest at the bottom. In other deep-water species the external form may frequently be explained as an adaptation to the special exigencies of the environment. Thus, for example, many species are provided with long stalks which lift up the body of the sponge out of the soft ooze m which it would otherwise be smothered, while the bottom of the stalk is frequently extended in root-like processes which serve to attach it to some solid object (e.g. Stylocordyla). In other cases the sponge supports itself on the surface of the ooze by long stiff processes, formed of bundles of spicules which radiate from the central, cap-shaped body; this is known as the “Crinorhiza form,” and is met with in several distinct genera (fig. 11). Amongst the Hexactinellida, which are essentially a deep-water group, many very beautiful external forms are met with, the best known, perhaps, being the so-called Venus's flower basket (Euplectella, fig. 12).
Flabellate (or fan-shaped) and cup-shaped forms are frequently met with even amongst shallow-water sponges, and in widely separated genera, such as Poterion (the great Neptune's cup sponge) and Reniera testudinaria. In Phyllospongia the flabellate and cup-shaped forms pass insensibly into one another, the cup being apparently merely a folded lamella. Slender branching forms are also not uncommon in shallow water, as seen in the common Chalina oculata of the British coast. Spherical forms, such as Tethya, likewise occur. By far the greater number of shallow-water sponges, however, are quite irregular in shape and either form crusts of varying thickness on the surface of rocks and sea-weed, or large and massive aggregates which may rise to a considerable height above the substratum. In the boring sponges (Family Clionidae) the sponge occupies an elaborate system of chambers and passages which it excavates for itself in the shells of Mollusca and other calcareous organisms. The common British Cliona celata begins