1. Amphidromous shrimps live and breed in freshwater rivers and streams, but their larvae require development in sea water. Larvae may hatch upstream and then drift to the sea, although in some species females have been reported to migrate to the coast before larvae are released. Here, we tested the relative importance of larval drift and female migration in Macrobrachium ohione (Decapoda: Palaemonidae) in a distributary of the Mississippi River in Louisiana, U.S.A. 2. Newly hatched (stage-1) larvae are nonfeeding and will not moult to stage 2 (first feeding stage) without encountering salt water. A factorial experiment was conducted in the laboratory to test the effects on moulting to stage 2 of (i) time spent by stage-1 larvae in fresh water before (ii) exposure to and maintenance in water of different salinity. Larvae kept in fresh water for 1 or 3 days before a change to saline water at 6 or 10 ppt showed a greater frequency of moulting than those kept for longer (5 days) in fresh water or changed to less saline water (2 ppt). Non-moulting larvae died or were moribund within 11 days of hatching. 3. The relative abundance of stage-1 larvae was measured with plankton tows at two locations in the river c. 150 km apart, one near the sea and one upstream. Larval abundances near the sea were significantly greater than those upstream. 4. The results indicate that hatched larvae of M. ohione have a limited period in which to drift in fresh water before reaching water sufficiently saline to stimulate moulting to the first feeding stage. Female migrations may play an important role in delivering larvae of amphidromous species from large continental river systems in which distances to the sea are great, while larval drift alone may be sufficient in species living in short streams, like those found in many small mountainous tropical islands.

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The sexual system of two caridean shrimps (Processa riveroi and P. bermudensis) was investigated, stimulated by reports of male to female sex change (protandry) in Processa edulis from European waters. Shrimps used in the study were obtained from monthly samples taken from March 1982 to February 1983 in a Thalassia -Syringodium seagrass meadow in Puerto Rico. Observations on size, sex, and reproductive condition were used to construct monthly size -frequency distributions and sex-ratios by size-class (SC). Males were smaller than reproductive females, but there was extensive overlap in size between males and immature females. A sex-ratio (SR) analysis by SC of the overall year-long population sample showed an equal or female-biased SR in the smallest SC, a male-biased SR in 1-3 intermediate SC, with larger SC dominated by females incubating embryos. Such a population structure might result from slower growth in males than females and higher mortality in larger males. Observations on and allometric analysis of sexual characters failed to identify transitional individuals (sex-changers) intermediate in reproductive morphology between males and females. Thus, a hypothesis of protandry is rejected, and that of gonochory (separate sexes) is accepted in these two Processa species, revealing possible variation in sexual systems among Processa species.

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Abstract. Macrobrachium ohione is a migratory (amphidromous) river shrimp (Decapoda, Caridea) that may be parasitized by the branchial parasite Probopyrus pandalicola (Isopoda, Bopyridae). The parasite disrupts gonadal maturation and spawning in female shrimps, resulting in the total loss of reproduction. Shrimps are usually infected by bopyrid parasites during the late zoeal or early postlarval stages; in this study, we investigated the apparent parasite infection of adult shrimps. We analyzed the relationships between parasite body size (total length) and host shrimp body size (carapace length) to test the hypothesis that parasite infection of adult shrimps occurs during the shrimps' reproductive migrations. The results presented here indicate that infection of adult shrimps is common in M. ohione in the Atchafalaya and Mississippi Rivers, Louisiana, USA. In the two upriver sites sampled, Butte La Rose (BLR) and River Bend (RB), parasite size was not associated with host body size. In these locations, many parasitized adult M. ohione were infected with immature P. pandalicola (40.3% in BLR and 51.2% in RB), indicating that the shrimps were adults at the time of infection. A possible explanation is that when female shrimps enter the estuary to hatch larvae, they molt and spawn another brood. The smaller male shrimps that accompany the females downstream are also assumed to molt and continue growth. The intermediate host of the parasite is an estuarine copepod, and thus the parasite cryptoniscus larva that infects the host shrimp is primarily estuarine as well. Newly molted shrimps have soft cuticles, which may facilitate their infection by parasite cryptonisci. Our conclusion is that most infections of adult shrimps occur during their migration into estuarine waters, the primary habitat of infective parasite larvae, and that host vulnerability is probably increased following host ecdysis.