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Sponges of the New Caledonian lagoon - IRD

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.,<br />

Matrix cyanobacleria<br />

(photo J. Vacelet)<br />

within <strong>the</strong> cavity on <strong>the</strong> concave side. In most encrusting and massive species<br />

oscules are placed on <strong>the</strong> ends <strong>of</strong> small stalks or conules, above <strong>the</strong> level <strong>of</strong> <strong>the</strong><br />

surface and away from <strong>the</strong> pores, to allow <strong>the</strong> excreted water to be flushed away<br />

from <strong>the</strong> sponge.<br />

Within <strong>the</strong> sponge <strong>the</strong> living 'tissue', bounded on all sides by <strong>the</strong> pinacoderm, is<br />

called <strong>the</strong> mesohyl, which includes all <strong>the</strong> area between <strong>the</strong> pinacocyte layers, or<br />

between pinacocytes and choanocytes, and between <strong>the</strong> canals and choanocyte<br />

chambers. The mesohyl contains a matrix or ground substance composed <strong>of</strong> a<br />

striated protein called collagen, an organic skeleton composed <strong>of</strong> spongin fibres,<br />

and/or an inorganic skeleton composed <strong>of</strong> mineral spicules. Within this mesohyl<br />

are found mobile totipotent cells, capable <strong>of</strong> changing function as required. Cell<br />

types can vary between taxonomic groups, although <strong>the</strong>ir recognition and cytological<br />

taxonomy is still poorly understood. These cells include generalised amoebocytic<br />

'stock' cells (archaeocytes) with large lobopods capable <strong>of</strong> active phagocytosis,<br />

as well as many o<strong>the</strong>r types that have become specialised to carry out particular<br />

functions within <strong>the</strong> sponge. Cells that produce <strong>the</strong> precursors <strong>of</strong> spongin<br />

fibres (collencytes) have filopods; those that secrete spicules (sclerocytes) are<br />

capable <strong>of</strong> incorporating silica or provoking a calcium deposit, and <strong>the</strong>se migrate<br />

to <strong>the</strong> area within <strong>the</strong> mesohyl where <strong>the</strong> mineral skeleton is being deposited;<br />

contractile cells occur around excurrent oscules (myocytes). Of <strong>the</strong> many sorts <strong>of</strong><br />

cells in sponges, known by <strong>the</strong>ir characteristic shape and organelles, only few so<br />

far have a known function or chemical structure. Attempts have been made to<br />

use <strong>the</strong>se cytological characters in a taxonomic framework but with limited<br />

success. In addition to <strong>the</strong>se native cells many species have symbiotic bacteria<br />

and cyanobacteria which play an important role in sponge nutrition in <strong>the</strong>se<br />

species.<br />

The distribution <strong>of</strong> cells within <strong>the</strong> mesohyl, <strong>the</strong> deposition <strong>of</strong> collagen and location<br />

<strong>of</strong> water current canals are more or less homogeneous within <strong>the</strong> sponge. In some<br />

massive sponges, however, it is possible to see a differentiated external layer several<br />

millimetres thick, which contains no choanocyte chambers. This ectosomal<br />

layer is streng<strong>the</strong>ned by collagen fibrils and <strong>of</strong>ten also a special mineral skeleton,<br />

clearly differentiated from <strong>the</strong> deeper choanosomal region. AS a consequence <strong>of</strong><br />

lacking developed tissues or organs sponges also lack a nervous system, nerve<br />

cells, coordination centre, head end or brain. They have only a low level <strong>of</strong> cellular<br />

31<br />

Sponge<br />

struc:ture

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