The gastrodermis of Atriaster heterodus Lebedev & Paruchin, 1969 (Polyopisthocotylea), a gill parasite from Diplodus argenteus (Valenciennes, 1830) The functional morphology of the digestive system has been studied for different Monogenea (Smyth & Halton 1983, Bogitsh 1993 and the feeding in polyopisthocotyleans and monopisthocotyleans is generally distinct with the former ingesting blood (Llewelyn 1954, Halton 1982 and the latter, mucus and epithelial cells. However, blood pigments were observed in a few monopisthocotyleans (Uspenskaya 1962, Kearn 1963, Fournier 1978, Buchmann et al. 1987) while Allen and Tinsley (1989) demonstrated blood and epithelial cells at the same time in the gut lumen of a polyopisthocotylean species.Atriaster heterodus Lebedev & Paruchin, 1969 (Polyopisthocotylea) was recently reported from Rio de Janeiro coast (Santos et al. 1996). Surface topography and ultrastructural aspects of the spermatogenesis of this species have been described by Santos et al. (1997). The ultrastructure of the gastrodermis and the nutrition of this species are described herein. This paper represents the first ultrastructural study of gut caeca and nutrition of a marine monogenean from Brazil.
MATERIALS AND METHODSParasites -Sixty five specimens of A. heterodus were obtained from the gills of 25 Diplodus argenteus (Valenciennes, 1830) Sparidae, collected in Copacabana beach, Rio de Janeiro, Brazil.Histochemistry -Monogeneans and gill filaments were fixed in 5% buffered formalin or 70% ethanol. Samples were embedded in paraffin and cut in 5 mM sections which were deparaffinized with xylene and prior to staining, hydrated in decreasing concentrations of ethanol to water. Histochemical reactions are indicated with the references and color of positive reactions as follows. Lilly and Fullmer (1976) were tested Perls (+=blue-green), Okajima (+=or-ange-red) and Dunn-Thompson (+= emerald green). The picric alcohol solubility test (Llewelyn 1954) was tested for hematin (+=solve).Ultrastructure -For ultrastructural studies, parasites were fixed for 2 hr at 4°C in a solution containing 4% paraformaldehyde, 2.5% glutaraldehyde and 0.3M sucrose in 0.1M cacodylate buffer in sea water, pH 7.2. After being washed in the same solution, they were post-fixed for 1 hr in dark conditions in a solution containing 1% OsO 4 , 0.8% potassium ferricyanide, and 5mM CaCl 2 in