Migration and habitat use of sea turtles in the Bahamas

Objectives: Evaluate movement and distribution patterns of sea turtles in our series of study sites in The Bahamas. This objective includes the questions of where do the turtles come from, how long are they resident in these sites, and where do they go when they leave. Collect data that will allow us to develop techniques to compare habitat quality and to serve as a foundation for studies of the role of green turtles in seagrass ecosystems. Evaluate models for estimating growth rates and carrying capacities for sea turtles based on our data from a long-term study of immature green turtles in the southern Bahamas. (Document has 7 pages.

Biology of pelagic sea turtles: effects of marine debris

Objectives: 1. Quantify the sub-lethal effect of debris ingestion (nutrient dilution) on nutrient gain 2. Model sub-lethal effects of debris ingestion on nutrient intake and growth 3. Evaluation of stress from entanglement on the loggerhead sea turtle 4. Movement patterns and behavior of pelagic-stage loggerheads in the eastern Atlantic 5. Document the genetic relationships of pelagic-stage loggerheads in the eastern Atlantic with rookeries in the southeast US (Document has 14 pages; lists publications resulting from research

Evaluating trends in abundance of immature green turtles, Chelonia mydas, in the Greater Caribbean

Many long-lived marine species exhibit life history traits. that make them more vulnerable to overexploitation. Accurate population trend analysis is essential for development and assessment of management plans for these species. However, because many of these species disperse over large geographic areas, have life stages inaccessible to human surveyors, and/or undergo complex developmental migrations, data on trends in abundance are often available for only one stage of the population, usually breeding adults. The green turtle (Chelonia mydas) is one of these long-lived species for which population trends are based almost exclusively on either numbers of females that emerge to nest or numbers of nests deposited each year on geographically restricted beaches. In this study, we generated estimates of annual abundance for juvenile green turtles at two foraging grounds in the Bahamas based on long-term capture-mark-recapture (CMR) studies at Union Creek (24 years) and Conception Creek (13 years), using a two-stage approach. First, we estimated recapture probabilities from CMR data using the Cormack-Jolly-Seber models in the software program MARK; second, we estimated annual abundance of green turtles. at both study sites using the recapture probabilities in a Horvitz-Thompson type estimation procedure. Green turtle abundance did not change significantly in Conception Creek, but, in Union Creek, green turtle abundance had successive phases of significant increase, significant decrease, and stability. These changes in abundance resulted from changes in immigration, not survival or emigration. The trends in abundance on the foraging grounds did not conform to the significantly increasing trend for the major nesting population at Tortuguero, Costa Rica. This disparity highlights the challenges of assessing population-wide trends of green turtles and other long-lived species. The best approach for monitoring population trends may be a combination of (1) extensive surveys to provide data for large-scale trends in relative population abundance, and (2) intensive surveys, using CMR techniques, to estimate absolute abundance and evaluate the demographic processes' driving the trends

Estimates of survival probabilities for oceanic-stage loggerhead sea turtles (Caretta caretta) in the North Atlantic

Estimates of instantaneous mortality rates (Z) and annual apparent survival probabilities (Φ) were generated from catch-curve analyses for oceanic-stage juvenile loggerheads (Caretta caretta) in the waters of the Azores. Two age distributions were analyzed: the “total sample” of 1600 loggerheads primarily captured by sighting and dipnetting from a variety of vessels in the Azores between 1984 and 1995 and the “tuna sample” of 733 loggerheads (a subset of the total sample) captured by sighting and dipnetting from vessels in the commercial tuna fleet in the Azores between 1990 and 1992. Because loggerhead sea turtles begin to emigrate from oceanic to neritic habitats at age 7, the best estimates of instantaneous mortality rate (0.094) and annual survival probability (0.911) not confounded with permanent emigration were generated for age classes 2 through 6. These estimates must be interpreted with caution because of the assumptions upon which catch-curve analyses are based. However, these are the first directly derived estimates of mortality and survival probabilities for oceanic-stage sea turtles. Estimation of survival probabilities was identified as “an immediate and critical requirement” in 2000 by the Turtle Expert Working Group of the U.S. National Marine Fisheries Service

Home range and habitat use by Kemp's Ridley turtles in West-Central Florida

The Kemp's ridley turtle (Lepidochelys kempii) is an endangered species whose recovery depends in part on the identification and protection of required habitats. We used radio and sonic telemetry on subadult Kemp's ridley turtles to investigate home-range size and habitat use in the coastal waters of west-central Florida from 1994 to 1996. We tracked 9 turtles during May-August up to 70 days after release and fou.ld they occupied 5-30 km2 foraging ranges. Compositional analyses indicated that turtles used rock outcroppings in their foraging ranges at a significantly higher proportion than expected. based on availability within the study area. Additionally. turtles used live bottom (e.g .• sessile invertebrates) and green macroalgae habitats significantly more than seagrass habitat. Similar studies are needed through'mt the Kemp's ridley turtles' range to investigate regional and stage-specific differences in habitat use. which can then be used to conserve important foraging areas

Pathogenic, Molecular, and Immunological Properties of a Virus Associated with Sea Turtle Fibropapillomatosis. Phase II : Viral Pathogenesis and Development of Diagnostic Assays

Research conducted under this RWO from July 1, 1997 through June 30, 2000 has provided important new information about the pathogenesis, virology, and immunology of marine turtle fibropapillomatosis. In particular, we have provided strong evidence for the association of a herpesvirus with fibropapillomatosis of the green turtle,Chelonia mydas, and the loggerhead turtle, Caretta caretta, in Florida. In addition we have provided new evidence for the absence of papillomaviruses from sea turtle fibropapillomas. Although unsuccessful, important new attempts were made to cultivate the FP-associated herpesvirus in vitro in collaboration with the National Wildlife Health Center. During this period of time, we completed publication of the first comprehensive description of the comparative pathology and pathogenesis of experimentally induced and spontaneous fibropapillomas of green turtles (Chelonia mydas). We initiated innovative studies on the persistence of a Chelonian herpesviruses in the marine environment demonstrating for the first time that the environmental survivability of Chelonian herpesviruses makes them real threats to marine turtle health. Finally, we explored development of a serological assay for FP using synthetic herpesvirus peptides and developed methodologies for detection of antibodies to LETV [Iung-eye-trachea virus] a disease-associated herpesvirus of the green turtle, Chelonia mydas.. This last initiative is ongoing and will further our efforts to develop specific immunological assays for the FP-associated herpesvirus and FP. (17 page document

Compensatory growth in oceanic loggerhead sea turtles: response to a stochastic environment

Compensatory growth (CG, accelerated growth that may occur when an organism that has grown at a reduced rate as a result of suboptimal environmental conditions is exposed to better conditions) is considered an adaptation to variable en vironments. Although documented thoroughly under captive conditions, CG has rarely been studied in wild populations. In their first years of life, oceanic-stage loggerhead sea turtles (Caretta caretta) have relatively little control over their geographic position or movements and thus have an extremely stochastic lifestyle with great variation in food availability and temperature. This environmental variation results in variable growth rates. We evaluate somatic growth functions of oceanic-stage loggerheads from the eastern Atlantic based on skeletochronology that allowed us to assign age and cohort to each individual. We demonstrate CG in these turtles based on three different analytical approaches: changes in coefficients of variation in size-at-age, generalized additive model regression analyses of somatic growth, and linear regression of age-specific growth rates. As a result of CG, variation in size-at-age in these juvenile loggerheads is substantially reduced. Thus, size is a better predictor of age than expected based on variation in growth rates. CG decreases with age, apparently as loggerheads gain greater control over their movements. In addition, we have evaluated for the first time in wild sea turtles the time-dependent nature of somatic growth by distinguishing among age, year, and cohort effects using a mixed longitudinal sampling design with assigned-age individuals. Age and year had significant effects on growth rates, but there was no significant cohort effect. Our results address critical gaps in knowledge of the demog raphy of this endangered species.info:eu-repo/semantics/publishedVersio

Green turtle somatic growth model: evidence for density dependence.

Abstract. The green turtle, Chelonia mydas, is a circumglobal species and a primary herbivore in marine ecosystems. Overexploitation as a food resource for human populations has resulted in drastic declines or extinction of green turtle populations in the Greater Caribbean. Attempts to manage the remaining populations on a sustainable basis are hampered by insufficient knowledge of demographic parameters. In particular, compensatory responses resulting from density-dependent effects have not been evaluated for any sea turtle population and thus have not been explicitly included in any population models. Growth rates of immature green turtles were measured during an 18-yr study in Union Creek, a wildlife reserve in the southern Bahamas. We have evaluated the growth data for both straight carapace length (SCL) and body mass with nonparametric regression models that had one response variable (absolute growth rate) and five potential covariates: sex, site, year, mean size, and recapture interval. The SCL model of size-specific growth rates was a good fit to the data and accounted for 59% of the variance. The body-mass model was not a good fit to the data, accounting for only 26% of the variance. In the SCL model, sex, site, year, and mean size all had significant effects, whereas recapture interval did not. We used results of the SCL model to evaluate a density-dependent effect on somatic growth rates. Over the 18 yr of our study, relative population density underwent a sixfold increase followed by a threefold decrease in Union Creek as a result of natural immigration and emigration. Three lines of evidence support a density-dependent effect. First, there is a significant inverse correlation between population density and mean annual growth rate. Second, the condition index (mass/(SCL) 3 ) of green turtles in Union Creek is positively correlated with mean annual growth rates and was negatively correlated with population density, indicating that the green turtles were nutrient limited during periods of low growth and high population densities. Third, the population in Union Creek fluctuated around carrying capacity during our study and thus was at levels likely to experience densitydependent effects that could be measured. We estimate the carrying capacity of pastures of the seagrass Thalassia testudinum, the major diet plant of the green turtle, as a range from 122 to 4439 kg green turtles/ha or 16-586 million 50-kg green turtles in the Caribbean. Because green turtle populations are probably regulated by food limitation under natural conditions, carrying capacity can serve as a baseline to estimate changes in green turtle populations in the Caribbean since preColumbian times and to set a goal for recovery for these depleted populations. Finally, we compare the growth functions for green turtle populations in the Atlantic and Pacific oceans. Not only does the form of the size-specific growth functions differ between the two regions (monotonic declining in the Atlantic and nonmonotonic in the Pacific), but also small juvenile green turtles in the Atlantic have substantially higher growth rates than those in the Pacific. Research is needed to evaluate the causes of these differences, but our results indicate that demographic parameters between ocean basins should only be extrapolated with great caution

Activity patterns of Kemp's ridley turtles, Lepidochelys kempii, in the coastal waters of the Cedar Keys, Florida

Radio and sonic telemetry were used to investigate the tidal orientation, rate of movement (ROM), and surfacing behavior of nine Kemp's ridley turtles, Lepidochelys kempii, tracked east of the Cedar Keys, Florida. The mean of mean turtle bearings on incoming (48 ± 49 0) and falling (232 ± 41 0) tides was significantly oriented to the mean directions of tidal flow (37±9°, P<0.0025, and 234±9 0, P<0.005, respectively). Turtles had a mean ROM of 0.44±0.33 km/h (range: 0.004-1.758 km/h), a mean surface duration of 18± 15 s (range: 1-88 s), and a mean submergence duration of 8.4± 6.4 min (range: 0.2-60.0 min). ROM was negatively correlated with surface and submergence durations and positively correlated with the number of surfacings. Furthermore, ROMs were higher and surface and submergence durations were shorter during the day. Daily activities of turtles were attributed to food acquisition and bioenergetics

Transatlantic developmental migrations of loggerhead sea turtles demonstrated by mtDNA sequence analysis

Molecular markers based on mitochondrial (mt) DNA control region se quences were used to test the hypothesis that juvenile loggerhead sea turtles (Caretta caretta) in pelagic habitats of the eastern Atlantic are derived from nesting populations in the western Atlantic. We compared mtDNA haplotypes from 131 pelagic juvenile turtles (79 from the Azores and 52 from Madeira) to mtDNA haplotypes observed in major nesting colonies of the Atlantic Ocean and Mediterranean Sea. A subset of 121 pelagic samples (92%) contained haplotypes that match mtDNA sequences observed in nesting colonies. Maximum likelihood analyses (UCON, SHADRACQ) estimate that 100% of these pelagic juveniles are from the nesting populations in the southeastern United States and adjacent Yucatan Peninsula, Mexico. Estimated contributions from nesting populations in south Florida (0.71, 0.72), northern Florida to North Carolina (0.19, 0.17), and Quintana Roo, Mexico (0.11, 0.10) are consistent with the relative size of these nesting aggregates. No contribution was detected from nesting colonies in the Mediterranean (Greece) or South Atlantic (Brazil), although samples sizes are insufficient to exclude these locations with finality. The link between west Atlantic nesting colonies and east Atlantic feeding grounds provides a more complete scientific basis for assessing the impact of subadult mortality in oceanic fisheries. Demographic models for loggerhead turtles in the western Atlantic can now be improved by incorporating growth and mortality data from juvenile turtles in pelagic habitats. These data demonstrate that the appropriate scale for loggerhead turtle conservation efforts is vastly larger than the current scale of management plans based on political boundaries.info:eu-repo/semantics/publishedVersio