Morphometric and chaetotactic studies were carried out on the body and cephalic regions of the rediae of Fasciola hepatica (Trematoda: Fasciolidae) in order to precisely identify the different redial generations of this trematode in Lymnaea truncatula under experimental infection. At day 49 post-exposure at 20°C, the length of the redia was significantly higher in the first group of the first generation (R1a) compared with successive generations, R1b, R2a and R2b/R3a. The width of the body was similar in the R1a, R1b, and R2a rediae, but was significantly lower in the R2b/R3a groups. The intrapharyngeal cavity of R1a rediae was significantly wider compared with the R1b, R2a, and R2b/R3a groups, whereas the pharyngeal wall was significantly thicker in the R2b/R3a rediae compared with the R1b and R2a groups. Four other measurements, namely the maximum length and width of the pharynx, diameter of the mouth, and width of intestine, also showed significant variations in relation to pharyngeal morphology and age of infection. Discriminant analysis based on these measurements demonstrated that 98% of the rediae were readily categorized into the four groups identified. The number of perioral sensillae ranged from 126 to 160 but a significant difference was only noted between the mean values of the first generation and those of the group R2b/R3a. From these parameters, the maximum width of the pharyngeal lumen was found to be the best characteristic in the identification of the redial generations.

The development of redial burden and cercarial shedding were studied in two groups of Lymnaea truncatula subjected to successive cross-exposures to one miracidium of Paramphistomum daubneyi and one of Fasciola hepatica per snail, or vice versa. The results were compared with those obtained in controls subjected to two unimiracidial exposures to the same trematode species. The infection rate was 61% in the group cross-exposed to P. daubneyi/F. hepatica and 37% in that cross-exposed to F. hepatica/P. daubneyi; it was 37% in the control group exposed to F. hepatica and 21% in that exposed to P. doubneyi. Snails harboring larval forms of both trematodes were few in number in cross-exposed groups and the redial burden was low, with one trematode dominating over the other. Free cercariae of F. hepatica and those of P. daubneyi were significantly more numerous at day 35 in the group cross-exposed to P. daubneyi/F. hepatica than in the controls or the other cross-exposed group. Mixed cercarial sheddings were obtained from 40% of snails with emission in the group cross-exposed to P. daubneyi/F. hepatica and from 21% of those in the F. hepatica/P. daubneyi group. The numbers of P. daubneyi metacercariae were significantly greater in the group cross-exposed to P. daubneyi/F. hepatica than in the other cross-exposed group, whereas no significant difference in mean numbers was noted for the F. hepatica cysts. Repartition of metacercariae over the patent period was clearly more irregular for P. daubneyi than for the other trematode.

Single-miracidium infections of Lymnaea truncatula by Fasciola hepatica were experimentally carried out to identify the redial generations of this trematode when the larval development was unusual (when the first-appearing mother redia, or R1a redia, died after its exit from the sporocyst). Four parameters were measured in the body and pharyngeal region at weekly intervals. At day 49 post-exposure at 20°C, the body of the second mother rediae (R1b) was significantly longer than that of the subsequent generations, R2a and R2b/R3a (a mean of 3.0 mm instead of 1.0 and 0.9 mm, respectively). The body was significantly wider in the R1b and R2a groups than in the R2b/R3a rediae. The pharyngeal lumen was significantly wider in the R1b group than in the R2a and R2b/R3a rediae (a mean of 48.6 μm instead of 10.8 and 3.3 μm at day 49). The thickness of the pharyngeal wall did not differ in the R1b and R2b/R3a groups, but was significantly lower in the R2a group (19.5 μm instead of 23.0-23.6 at day 49). There was better development of R1b and R2b/R3a rediae in the snails when the R1a redia died, compared with normal larval development (with a living R1a redia).

Fasciola hepatica mother rediae belonging to the first generation and the first cohort of the second generation were extracted from their snail intermediate host (Lymnaea truncatula) and maintained in vitro for 16 days to determine the quantity of daughter rediae and cercariae produced by each generation. L-15 Leibovitz medium with a saline fraction adjusted to that of the L. truncatula hemolymph was used for experiments. A total of 35 daughter rediae exited from the 21 mother rediae of the first and second generations, which were 14-32 days old at the onset of culture. Microscope examination of the mother rediae demonstrated the presence of numerous redial embryos and differentiating daughter rediae, whereas no cercaria was seen within their body. A total of 49 cercariae exited from the 17 mother rediae of the first and second generations, which were 29-50 days old at the onset of culture. No differentiating daughter redia was seen in these last mother rediae. The productivity of the first or second generation (first cohort) was nearly identical in terms of cercariae.