Tradeoff between establishing an infection and killing the host: response of snails ( Physa acuta) to a gradient of trematode (Halipegus eccentricus) exposures.

Pond snails ( Physa acuta ) were exposed to a gradient (0, 1, 3, 5, 10, 15, 20, 25, 30, 35, 40, and 50) of trematode (Halipegus eccentricus) eggs and observed to determine egg dose effects on the survival of snails through the prepatent period, snail reproduction, and the production of cercariae. The probability of snail survival through the prepatent period significantly decreased with increasing egg exposures, where the odds of snail survival was 0.94 per trematode egg. Similarly, the probability of snail reproduction significantly decreased with increasing egg exposures, where the odds of snail reproduction was 0.85 per trematode egg. In contrast, the probability of a snail shedding cercariae significantly increased with increasing egg exposures, where the odds of reaching a patent infection were 1.64 per trematode egg. However, snails shedding cercariae that were exposed to higher doses of trematode eggs tended to die sooner. Thus, there appears to be a tradeoff between infecting a snail and killing the host.

Alternative life cycle strategies of Megalodiscus temperatus in tadpoles and metamorphosed anurans.

Megalodiscus temperatus (Stafford, 1905) is a common paramphistome trematode of North American amphibians with a two host life cycle and has been reported to infect frogs and rarely tadpoles. In this study we document the alternative life cycle strategy of M. temperatus in tadpoles and metamorphosed anurans. We show through field work and experimental infections that M. temperatus can establish in both anuran life stages and worms become gravid and release eggs in both tadpoles and metamorphosed frogs. However, worms exhibit differences in route of infection, development, egg production, and diet in tadpoles and metamorphosed anurans. These alternative life history strategies of M. temperatus suggest different selective pressures on the development and reproductive success of these worms in tadpoles and metamorphosed anurans, and we discuss the evolutionary avenues for and constraints on amphibian trematode life cycles presented by these two different anuran life stages.

Gregarina niphandrodes (Eugregarinorida: Septatorina): oocyst surface architecture.

The surface architecture of oocysts produced by Gregarina niphandrodes (Eugregarinorida) from Tenebrio molitor adults (Coleoptera: Tenebrionidae) as revealed by scanning electron microscopy is reported. Gametocysts were allowed to dehisce on 15-mm, round cover glasses; the cover glasses with their oocysts chains were then mounted on stubs without further processing, and sputter-coated with 20-nm gold palladium. Scanning electron microscopy was performed at 10-15 kV with a Hitachi 3000N SEM. Oocysts retained their characteristic shapes as reported in the original species description but showed longitudinal ridges of relatively uniform height, width, and spacing, in separate fields on either side of a central equatorial bulge in the oocysts. There was no ultrastructural evidence of an enclosing external sheath holding the oocysts in a chain. Oocyst ends were flared slightly, and the chain itself was twisted, with adjacent oocysts offset slightly from one another. This article now provides an additional set of structural characters potentially useful in gregarine systematics.

New and emended descriptions of gregarines from flour beetles (Tribolium spp. and Palorus subdepressus: Coleoptera, Tenebrionidae).

The following new gregarine taxa are described from larvae of flour beetles (Coleoptera: Tenebrionidae): Awrygregarina billmani, n. gen., n. sp., from Tribolium brevicornis; Gregarina cloptoni, n. sp., from Tribolium freemani; Gregarina confusa, n. sp., from Tribolilum confusum; and Gregarina palori, n. sp., from Palorus subdepressus. In addition, the description of Gregarina minuta Ishii, 1914, from Tribolium castaneum, is emended. Scanning electron micrograph studies of these species' oocysts reveal differences in surface architecture. The Gregarina species have oocysts with longitudinal ridges, visible with SEM, whereas Awrygregarina billmani oocysts have fine circumferential striations; surface architecture is the main feature distinguishing the 2 gregarine genera. Although parasites from adult beetles are not included in the descriptions, adults of all host species can be infected experimentally using oocysts from the new taxa.