Abstract
The heart-body in Neoamphitrite figulus (Dalyell) forms a mass of tissue within the supra-oesophageal vessel almost occluding the lumen. The tissue forms a much-infolded cylinder enclosed by a basal lamina consisting of a fibrous reticulum through which the assembled haemoglobin molecules are discharged into the plasma (Dales & Pell, 1970). A function of both the heart-body and the extravasal (‘chloragogen’) tissue in polychaetes without a heart-body was established by biochemical analysis (Kennedy & Dales, 1958; Dales, 1963, 1965) to be the synthesis of plasma haemoglobin (erythrocruorin) or chlorocruorin. This was confirmed by electron microscopy (TEM) by Breton-Gorius (1963) in Arenicola, Potswald (1969) in Spirorbis, Dales & Pell (1970) in Neoamphitrite, Lattice, Myxicola, Megalomma and Sabella, and by Friedmann & Weiss (1980) in Amphitrite. It would appear that the same tissues also sequester phagocytosed materials (Braunbeck & Dales, 1984). Re-examination of this tissue by trans-mission electron microscopy (TEM) has extended our knowledge of the ultra-structure. Here we discuss these results in relation to the function of these tissues in the production of the respiratory pigments found in the plasma. Some heart-bodies of Terebella lapidaria L., Lattice conchilega (Pallas) and Cirriformia tentaculata (Montagu) have also been examined by TEM for comparison with that of Neoamphitrite figulus.
Publisher
Cambridge University Press (CUP)
Cited by
9 articles.
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