Among reptiles that show temperature-dependent sex determination, sex ratios vary across constant incubation temperatures in ways sufficiently predictable to allow classification into patterns. One common pattern shows low temperatures yielding only males and high temperatures yielding only females. Another common pattern has low as well as high temperatures yielding only or mostly females and some intermediate temperatures yielding mostly males. Patterns tend to be associated with the direction of sexual dimorphism in adult size, especially for species with strong dimorphism.Pivotal temperatures (those yielding 1:l sex ratios) within the best-documented species and genera tend to increase with both latitude and longitude across central and southern North America. These geographic trends probably reflect factors that affect nest temperatures (duration of growing season, insolation, and prevailing amounts of shading by vegetation).Data from a population of the alligator snapping turtle (Macroclemys temminckii) suggest that some embryos are temperature-independent females because these individuals become females even when they are shifted among male-producing temperatures during development. These individuals are also more frequent in clutches of small eggs. In this and several other species, no constant incubation temperatures yield more than 75% males. 0 1994 WiIey-Liss, Inc.

Because particular life history traits affect species vulnerability to development pressures, cross-species summaries of life history traits are useful for generating management guidelines. Conservation of aquatic turtles, many members of which are regionally or globally imperiled, requires knowing the extent of upland habitat used for nesting. Therefore, we compiled distances that nests and gravid females had been observed from wetlands. Based on records of > 8000 nests and gravid female records compiled for 31 species in the United States and Canada, the distances that encompass 95% of nests vary dramatically among genera and populations, from just 8 m forMalaclemys to nearly 1400 m for Trachemys. Widths of core areas to encompass varying fractions of nesting populations (based on mean maxima across all genera) were estimated as: 50% coverage = 93 m, 75% = 154 m, 90% = 198 m, 95% = 232 m, 100% = 942 m. Approximately 6-98 m is required to encompass each consecutive 10% segment of a nesting population up to 90% coverage; thereafter, ca. 424 m is required to encompass the remaining 10%. Many genera require modest terrestrial areas (zones) for 95% nest coverage (Actinemys, Apalone, Chelydra, Chrysemys, Clemmys,Glyptemys, Graptemys, Macrochelys, Malaclemys, Pseudemys, Sternotherus), whereas other genera require larger zones (Deirochelys, Emydoidea, Kinosternon, Trachemys). Our results represent planning targets for conserving sufficient areas of uplands around wetlands to ensure protection of turtle nesting sites, migrating adult female turtles, and dispersing turtle hatchlings. Our results represent planning targets for conserving sufficient areas of uplands around wetlands to ensure protection of turtle nesting sites, migrating adult female turtles, and dispersing turtle hatchlings.

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The Suwannee Cooter, Pseudemys concinna suwanniensis, the largest member of the speciose turtle family Emydidae, inhabits a small number of rivers that drain into the northeastern Gulf of Mexico along the northwest coast of Florida from just west of Tallahassee to just south of Tampa. The status of this state-protected subspecies in the southernmost of these rivers, the Alafia, is unknown and hence of conservation concern. We provide recent evidence confirming that a reproducing population still exists in this river, and review available specimens and both published and unpublished records documenting the southern limit of distribution. At least within the eastern United States, our observations also extend confirmed knowledge of the geographic occurrence of hatchling turtles overwintering in the nest southward by 285 km.