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Stage durations are integral to wildlife population models that can inform management, as they influence age at maturation and stage-specific survival rates. To refine oceanic stage duration estimates for western North Atlantic loggerhead sea turtles Caretta caretta, skeletochronological analysis was conducted on humeri collected in the Azores islands and along the US Atlantic coast. Complementary skeletal growth increment-specific stable isotope analysis was also performed for a sub-set of the humeri, to identify the skeletal growth mark associated with the shift from oceanic to neritic habitat through stable nitrogen isotope (δ 15 N) values and the presence of turtles in inshore waters. Although the transitional growth mark in this sub-sample corresponded to a range of sizes similar to those described in previous studies, mean size at recruitment (55.3 cm straightline carapace length [SCL]) for these turtles was larger than previously estimated. Similarly, while the range of ages at recruitment -corresponding both with the transitional growth mark and those yielded by fitting smoothing splines to SCL-at-age data -overlapped almost fully with earlier estimates, the mean age estimate (12.4 yr) differed from previous studies. Validated back-calculation of somatic growth rates from skeletal growth marks yielded means and ranges that encompassed those of previous loggerhead growth studies in this geographic area. Generalized additive models and generalized additive mixed models used to assess the potential influence of discrete and continuous covariates on back-calculated growth rates spanning 1984 to 2009 indicated significant effects of age, SCL, calendar year, and δ 15 N, but none for sex or location.

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Green turtles Chelonia mydas are listed as Endangered on the IUCN Red List, yet in the South Pacific few conservation-relevant data are available for the species, especially relating to foraging and habitat use. Here, in situ observations and stable isotope analysis (δ13C and δ15N) were used to evaluate green turtle diet and recruitment patterns at Yadua Island and Makogai Island, Fiji. Juvenile green turtles (N = 110) were hand-captured, measured, and sampled. Stable isotope analysis was performed on skin samples and on putative prey items. ‘Resident’ turtles versus ‘recent recruits’ were classified based on their bulk skin tissue isotope values, which were compared with stable isotope values of local prey items and analyzed via cluster analysis. Green turtle diet composition was estimated using MixSIAR, a Bayesian mixing model. Recent recruits were characterized by ‘low δ13C/high δ15N’ values and ranged in curved carapace length (CCL) from 25.5 to 60.0 cm (mean ± SD = 48.5 ± 5.7 cm). Recruitment mostly occurred in summer. Green turtles identified as ‘residents’ had CCLs ranging from 43.5 to 89.0 cm (mean ± SD = 57.4 ± 9.0 cm) and were characterized by ‘high δ13C/low δ15N’ values; mixing model results indicate they fed primarily on invertebrates (40%), fishes (31%), and marine plants (29%). This study confirms the value of seagrass pastures as both an essential habitat and a primary food source for green turtles, and can serve as a baseline for evaluations of natural and anthropogenic changes in local green turtle aggregations.