The purpose of this study was to determine whether branched-chain amino acid (BCAA) supplementation attenuates indirect indicators of muscle damage during endurance exercise as compared with an isocaloric, carbohydrate (CHO) beverage or a noncaloric placebo (PLAC) beverage. Nine untrained men performed three 90 min cycling bouts at 55% VO 2peak. Subjects, blinded to beverage selection, ingested a total of 200 kcal of energy via the CHO or BCAA beverage before and at 60 min of exercise, or they drank the PLAC beverage. Creatine kinase (CK), lactate dehydrogenase (LDH), isokinetic leg-extension and -flexion torque, and muscle soreness were assessed before and immediately, 4 h, 24 h, and 48 h postexercise. The trials were separated by 8 wk. CK activities were significantly lower after the BCAA trial than in the PLAC trial at 4, 24, and 48 h postexercise, as well as lower than the CHO beverage at 24 h postexercise. CK was lower in the CHO trial at the 24- and 48-h time points than in the PLAC trial. LDH activities were lower in the BCAA trial at 4 h than in the PLAC trial. As compared with the CHO and PLAC trials, ratings of perceived soreness were lower at 24 h postexercise, and leg-flexion torque was higher at the 48-h time point after the BCAA trial. The present data suggest that BCAA supplementation attenuates muscle damage during prolonged endurance exercise in untrained college-age men. CHO ingestion attenuates CK activities at 24 and 48 h postexercise as compared with a placebo beverage.

Management of species of conservation concern requires knowledge of demographic parameters, such as rates of recruitment, survival, and growth. In the Caribbean, hawksbill turtles (Eretmochelys imbricata) have been historically exploited in huge numbers to satisfy trade in their shells and meat. In the present study, we estimated growth rate of juvenile hawksbill turtles around Anegada, British Virgin Islands, using capture–mark–recapture of 59 turtles over periods of up to 649 days. Turtles were recaptured up to six times, having moved up to 5.9 km from the release location. Across all sizes, turtles grew at an average rate of 9.3 cm year−1 (range 2.3–20.3 cm year−1), and gained mass at an average of 3.9 kg year−1 (range 850 g–16.1 kg year−1). Carapace length was a significant predictor of growth rate and mass gain, but there was no relationship between either variable and sea surface temperature. These are among the fastest rates of growth reported for this species, with seven turtles growing at a rate that would increase their body size by more than half per year (51–69% increase in body length). This study also demonstrates the importance of shallow water reef systems for the developmental habitat for juvenile hawksbill turtles. Although growth rates for posthatching turtles in the pelagic, and turtles larger than 61 cm, are not known for this population, the implications of this study are that Caribbean hawksbill turtles in some areas may reach body sizes suggesting sexual maturity in less time than previously considered.

We present the result of a multi-annual assessment of the spatio-temporal patterns of marine turtle nesting, and foraging in the Eastern Caribbean archipelago state of the British Virgin Islands. Despite exploitation over several centuries, three species (leatherback Dermochelys coriacea, green Chelonia mydas and hawksbill Eretmochelys imbricata turtles) are still nesting and green and hawksbill turtles are found foraging. Leatherback turtles are showing signs of a recovery co-incident with the implementation of an effective moratorium on adult take. When compared with historical data we demonstrate an apparent reduction in nesting levels in green and hawksbill turtles and a nesting range contraction in green turtles. Despite current conservation steps, it will be a decade or more before evidence of recovery can be expected in the two hard-shelled species. Coupled with wider biological knowledge, our findings offer insights into the relative resilience of the different species to exploitation pressure. Additionally, the intra-annual temporal and spatial spread of nesting demonstrated underlines the difficulties of monitoring such a multi-species assemblage in such a diffuse archipelago.

Evolutionary theory predicts that male and female offspring should be produced at a 1:1 ratio, but this may rarely be the case for species in which sex is determined during incubation by temperature, such as marine turtles. Estimates of primary sex ratio suggest that marine turtle sex ratios are highly skewed, with up to 9 females per male. We captured juvenile hawksbill turtles Eretmochelys imbricata in waters around Anegada, British Virgin Islands, a regionally important foraging aggregation, and analysed concentrations of plasma testosterone and oestradiol-17β from 62 turtles to estimate sex ratio. There were 2.4 to 7.7 times more females than males. Testosterone concentrations correlated with sampling date and sea surface temperature (SST), with higher con centrations in the late summer when SST was highest, suggesting that assigning sex through threshold values of sex hormones must be carried out cautiously. The sex ratio in the juvenile foraging aggregation around Anegada is more male biased than at other locations, suggesting that turtles at Anegada have resilience against feminising effects of climate change. Future work should (1) integrate the relative contributions of different genetic stocks to foraging aggregations and (2) investigate the annual and seasonal cycles of sex hormones, and differences among individuals and life history stages. KEY WORDS: Marine turtles · Sex ratio · Climate change · HormonesResale or republication not permitted without written consent of the publisher Aquat Biol 18: 9-19, 2013 Skewed sex ratios may be advantageous under specific biological circumstances (e.g. if pa rental investment in the sexes is unequal, if one sex helps their parents or if male siblings compete for mates), but also in some environmental circumstances (Warner & Shine 2008). The Charnov-Bull model (Charnov & Bull 1977) was proposed to ex plain this and has been demonstrated for a lizard species, such that offspring raised in conditions that promote high fitness for females had higher lifetime reproductive success if they were female than male (males were produced by hormonal manipulation at temperatures that usually lead to the development of females; Warner & Shine 2008). Temperature-dependent sex determinationIn marine turtles, sex is determined by the temperature experienced during the middle third of the embryo incubation period (temperature-dependent sex determination [TSD], a type of ESD), where males are produced at lower temperatures and females at higher temperatures (Yntema & Mrosovsky 1980, 1982, Mrosovsky 1988. The majority of research into sex ratios of marine turtles has been carried out on the nesting beach at the hatchling stage, and approaches using the modelled relationship between incubation temperature and sex ratio, as well as incubation duration and sex ratio, have enabled estimation of 'primary' sex ratio for a large number of rookeries (reviewed in Hawkes et al. 2009). Primary sex ratios vary among beaches and within clutches, as well as during the course of a nest...

No abstract