JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org.. Ecological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Ecology.Abstract. Turtles provide excellent models for studies of life history strategies, but terrestrial species are underrepresented in these analyses. We present a life table and demographic parameters of an inland population of Gopherus berlandieri to contribute to the study of evolution of turtle life histories. Data were gathered during a mark-recapture and radiotelemetry study in the Tamaulipan Biotic Province in southern Texas, USA. A total of 835 individuals were captured, measured, and their ages estimated. Females matured at 131 mm carapace length at an average of 5 yr of age (range: 4-8 yr). Clutch size, as determined by ultrasound, averaged 2.07 ?+ 0.15 eggs (n = 49). No nests were found, and we estimated clutch frequency with a quadratic model to be 1.34 clutches-female-t-year-1. Survival was estimated from age frequency regression and telemetry. Annual male survival (0.828, 0.834) differed (P < 0.05) from female survival (0.728, 0.774) for both techniques of estimation. Age-specific female survival ranged from 0.62 to 0.83 for 5-to 15-yr-old tortoises. Differential mortality of sexes led to a male-biased sex ratio in older age classes. Age structures of captured individuals did not vary (P > 0.05) among years, and population estimates did not differ among years; therefore, we constructed a life table under the assumption of a stationary population (r = 0.0). Under this assumption, survival from nest to age 4 yr must be at least 0.245, with hatchling survival of 0.528 to maintain a stationary population. Gopherus berlandieri matured at an earlier age, had smaller clutch sizes, and exhibited lower rates of female survival than other Gopherus species. We propose a physiological mechanism for lower female survival that implies trade-offs among egg size, subsequent hatchling survival, and female health. We maintain that high hatchling survival is necessary for population persistence. In an evolutionary context, we theorize that the selective advantages of small size and the life history strategies of G. berlandieri have been and are critical to its persistence.
Responses of woody plant communities on native rangelands in the western South Texas Plains to fire are not clearly understood. Our objective was to compare woody plant cover, density, and diversity on burned and nontreated rangelands. Five rangeland sites that received 2 dormant-season burns, 5 rangeland sites that received a combination of 1 dormant-season and 1 growing-season burn, and 5 sites of nontreated rangeland were selected on the Chaparral Wildlife Management Area, Dimmit and La Salle Counties, Tex. Woody plant cover was estimated using the line intercept method, and stem density was estimated in 25-x 1.5-m plots. Species richness did not differ among treatments. Percent woody plant cover was reduced by 50 and 41 % on winter and winter-summer combination burned sites, respectively. Honey mesquite (Prosopis glandulosa Torr.), twisted acacia (Acacia schaffneri S. Wats.), Texas persimmon (Diospyros texana Scheele), lotebush [Ziziphus obtusifolia (Hook.) T. & G.], wolfberry (Lycium berlandieri Dunal), and tasajillo (Opuntia leptocaulis Cand.) canopy cover was greatest on nontreated sites. Woody plant density declined by 29 and 23% on winter and winter-summer combination burned sites, respectively. Density of guayacan (Guajacum angustifolium Engelm.), wolfberry, and tasajillo was less on all burning treatments. Percent cover of spiny hackberry (Celtis pallida Torr.) and density of Texas pricklypear (Opuntia engelmannii Salm-Reif.-Dyck) declined on winter burned sites. Inclusion of summer fire into the burning regime did not increase declines in woody plants. Fire created a post-fire environment which resulted in the decline of many woody plant species. It is unclear to what degree other environmental factors such as herbivory and competition between woody plants and among woody and herbaceous vegetation may have interacted with fire in producing woody plant declines. Fire may be a useful tool in managing woody vegetation on native south Texas rangelands, while maintaining woody plant diversity.
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