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The life cycle of a senegalese strain of Fasciola gigantica was carried out in France from adults recovered in the liver of naturally infected cattle (Bos taurus). Laboratory-reared Lymnaea natalensis experimentally infected shed numerous cercariae. Metacercariae were used for successful infection of sheep. In the miracidium, variations are observed in the disposition of the medio-ventral epithelial cell of the second tier. The distribution of the superficial argentophilic structures is similar to that of the miracidium of F. hepatica. The chaetotaxy of the cercaria is very closely related to that of the cercaria of a strain of F. gigantica from Madagascar shed by Lymnaea hovarum but it differs clearly from that of the cercaria of F. hepatica. The encystment of a great number of cercariae (25 %) on the surface of water suggests that this is an important factor in the extension of the foci of contamination, and therefore increases greatly the risks of infection not only for animal but also for man. It is possible that human fascioliasis caused by F. gigantica is a disease, the importance of which is under-estimated.

Superficial argentophilic structures of the miracidium and cercaria of Paramphistomum phillerouxi Dinnik, 1961, are descrifed in detail. Concerning the miracidium they are similar to those of the miracidia of some species belonging to the genus. On the other hand the chaetotaxy of the cercaria is different from that of the cercaria of P. togolense (Alberet et coll., 1978) and therefore this appears to constitute a good criterium for the taxonomy of this group.

Cercarial chaetotaxy of Gastrodiscus aegyptiacus (Paramphistomoidea), parasite of the Horse, is described. Cercariae were shed by experimentally infected Bulinus forskalii. This description is the first one of a Gastrodiscidae. The cercarial chaetotaxy of the Gastrodiscidae is quite different from those of Paramphistomoidea and Diplodiscidae.

Study by SEM of the anterior dorsal teguments of male Schistosoma haematobium from infected rodents. Only paired males, at least hundred days post infection, display a typical morphology. Differentiation from other closely related species obtained experimentally from rodents is possible: bovis: no spines on the tubercles; haematobium: tubercles 10 to 15 microns wide with closely packed spines; curassoni: tubercles over 15 microns wide, with large, closely packed spines; intercalatum: tubercles under 10 microns wide, with scattered spines. It is suggested that the three haematobium genotypes A, B and D are slightly different: A: pointed spines, numerous small additional spines between the tubercles; B: pointed spines, no small additional spines between the tubercles; D: blunt spines. Moreover, the lengths of the prepatent periods in the molluscs of the three S. haematobium genotypes are possibly different: A 72-86 days, B 38-46 days, D 55-58 days. The differentiation of A, B and D is supported by limited data and conclusions on this particular aspect are presented only as a working hypothesis.

Study of Senegal cercariae emitted by naturally infected snails or by snails experimentally infected using eggs from human urine or from sheep liver, and study of the corresponding eggs. The relative position of the dorsal sensillae of cercariae is described by an "AD index" and the ratio length/width of eggs by an "L/l index." At the present time, we have not finished the epidemiological studies, certain experiments are imperfect and the isoenzyme analysis of the corresponding adults is incomplete. Nevertheless information given by the indices AD and L/l agree and lead us to admit the existence of a Schistosome different to mattheei, haematobium and bovis and which, following Brumpt and Gretillat we refer to as Schistosoma curassoni. If one relies on the indices, the study indicates that: a) S. mattheei has not been found in Senegal, b) S. bovis is quite rare, c) S. haematobium apparently exists in pure infections in Casamance and in mixed infections with S. curassoni in man in the north and in the east, d) S. curassoni is apparently the dominant species in domestic ruminants and in man in the north and in the east, e) Bulinus umbilicatus is the principal vector of S. curassoni and S. haematobium.

The life cycle of a Paramphistome from North Senegal is completed starting from cercariae shed by naturally infected Isidora guernei: a sheep and then uninfected Isidora guernei were successively infected experimentally. Adults obtained were identifiable as P. phillerouxi or as P. microbothrium. Species determination cannot be made on the basis of argentophilic structures in the miracidium. Morphology of sporocysts and rediae differs from that observed in P. phillerouxi but is undistinguishable from that described in P. microbothrium. Cercarial chaetotaxy differs from that of P. phillerouxi. Mollusc host: Isidora guernei belongs to the same genus as Isidora truncata and I. alluaudi, reported hosts to P. microbothrium. Therefore the material is provisionally identified as P. microbothrium. To confirm this, a strain of P. microbothrium from naturally infected Bos taurus in Egypt was studied. Miracidia were used to experimentally infect Isidora truncata; cercariae obtained were identical to those previously described for this species from I. truncata and I. alluaudi. Cercarial chaetotaxy was not significantly different from that of material from North Senegal. They represent therefore two strains of Paramphistomum microbothrium.