(WHO 1984, Madsen 1990, Sturrock 1995, Pointier & Giboda 1999. In the West Indies, the thiarid Melanoides tuberculata was effective in the elimination or reduction of populations of Biomphalaria glabrata, the intermediate host in the cycle of schistosomiasis , 1991a, Pointier & McCullough 1989, Pointier & Guyard 1992, Pointier 1993, Schlegel et al. 1997. However, in Venezuela M. tuberculata was introduced in 20 sites, but only in three sites was Biomphalaria spp. eliminated or effectively reduced (Pointier et al. 1991c). In Brazil, the first occurence of M. tuberculata was reported in 1967, in Santos, State of São Paulo. After that, this snail has spread to other localities, probably as a result of successive accidental introductions associated with fish farms (Vaz et al. 1986). However, there are few reports of interaction between M. tuberculata and species of the genus Biomphalaria in Brazil. glabrata reached a larger size and produced more cercaria of S. mansoni (Moné 1991). These results point to the dangers of species introductions for biological control based on poor knowledge and weak assumptions of species interactions. The effectiveness of M. tuberculata for biological control of B. glabrata in a specific environment can be evaluated only when the ecology of these species and the nature of their interactions are understood.Here, our objectives were to test two hypotheses: that M. tuberculata has a negative effect on the growth and demography of B. glabrata (H1), and that a substance liberated by M. tuberculata causes this negative effect (H2). The second hypothesis was proposed previously for Thiara granifera, another thiarid (Prentice 1983, Gomez et al. 1990, Perez et al. 1991. Two laboratory experiments were performed to test these hypotheses.
MATERIALS AND METHODSIndividuals of M. tuberculata and B. glabrata were collected in streams of two valleys in the municipality of Sumidouro, RJ, Brazil (22 o 02'59"S, 42 o 40'29"W). In laboratory, these individuals were raised in 74 x 237 x 330 mm plastic containers with 2 l of dechlorinated tap water. Dehydrated lettuce and rodent food pellets (3-4 mm large) were provided ad libitum, and temperature varied between 22 and 27 o C during the study. Containers were checked at least every two days to remove dead individuals, to guarantee ad libitum food, and that rodent pellets stayed on the bottom. The water was changed every fortnight to avoid any crowding effect, when the number of egg masses, embryos, young and adults was counted. These