ABSTRACT.Hawksbill sea turtles (Eretmochelys imbricata) inhabiting the eastern Pacific Ocean are one of the world's most threatened marine turtle management units. Despite the fact that knowledge about the status of sea turtles at foraging grounds is a key element for developing the effective conservation strategies, comprehensive studies of hawksbills at foraging habitats in the eastern Pacific remain lacking. For many years anecdotal information indicated Coiba Island National Park in Panama as a potentially important hawksbill foraging ground, which led to the initiation of monitoring surveys in September 2014. Ongoing mark-recapture surveys to assess population status, generate demographic data and identify key foraging sites have been conducted every six months in the park since that time. To date, a total of six monitoring campaigns consisting of four days each have been conducted, leading to the capture and tagging of 186 hawksbills, 51 of which were recaptured at least once. The size range of captured individuals was 30.0 to 75.5 cm and largely comprised of juveniles. Somatic growth rates of individual hawksbills were highly variable, ranging from -0.78 to 7.1 cm year -1 . To our knowledge, these are the first published growth rates for juvenile hawksbill turtles in the eastern Pacific Ocean. When these growth data are combined with information on hawksbill demography and distribution, our findings indicate Coiba Island National Park is one of the most important known foraging sites for hawksbill sea turtles in the eastern Pacific Ocean.

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Catchment hydrology is influenced by land‐use change through alteration of rainfall partitioning processes. We compared rainfall partitioning (throughfall, stemflow and interception) and soil water content in three land‐use types (primary forest, secondary forest and agriculture) in the Santa Fe region of Panama. Seasonal patterns were typified by larger volumes of throughfall and stemflow in the wet season, and the size of precipitation events was the main driver of variation in rainfall redistribution. Land‐use‐related differences in rainfall partitioning were difficult to identify due to the high variability of throughfall. However, annual throughfall in agricultural sites made up a larger proportion of gross precipitation than throughfall in forest sites (94 ± 1, 83 ± 6 and 81 ± 1% for agriculture, primary and secondary forests, respectively). Proportional throughfall (% of gross precipitation becoming throughfall) was consistent throughout the year for primary forest, but for secondary forest, it was larger in the dry season than the wet season. Furthermore, proportional stemflow in the dry season was larger in secondary forest than primary forest. Stemflow, measured only in primary and secondary forests, ranged between 0.9 and 3.2% of gross precipitation. Relative soil moisture content in agricultural plots was generally elevated during the first half of the dry season in comparison to primary and secondary forests. Because throughfall is elevated in agricultural plots, we suggest careful management of the spatial distribution and spread of this land‐use type to mitigate potential negative impacts in the form of floods and high erosion rates in the catchment. Copyright © 2013 John Wiley & Sons, Ltd.

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Summary1. Many prey species are chemically defended and have conspicuous appearance to deter predators (i.e. aposematism). Such warning signals work because predators pay attention to the colour and size of signals, which they associate with unprofitability. 2. Paradoxically, in early life stages, aposematic species are often warningly coloured, but their chemical defences are lacking because they have yet to be acquired through the diet or synthesized endogenously. This state of being conspicuous yet poorly defended must place individuals at increased risk of predation, but how they minimize this risk during development is unclear. 3. We reared larval green and black poison frogs (Dendrobates auratus) on a relatively low or a higher food supply and tested the hypothesis that individuals with more resources should grow larger while reducing their investment in warning signals at metamorphic completion. We also assayed markers of oxidative balance (malondialdehyde, superoxide dismutase and total antioxidant capacity) to ascertain whether there were resource-allocation trade-offs that differed with diet treatments. 4. Low-food froglets were relatively small, and their body size and signal luminance (perceived brightness) were positively correlated. In contrast, in high-food froglets body size and warning signal luminance were negatively correlated, suggesting either a resource-allocation trade-off or alternatively a facultative reduction in luminance exhibited by larger froglets. 5. The reduction in luminance in relatively large, high-food froglets did not appear to arise because of oxidative stress: signal luminance and markers of oxidative stress were positively correlated in high-food froglets, but were negatively correlated in low-food froglets suggesting a trade-off. 6. Our results highlight developmental plasticity in body size and coloration as affected by resource (i.e. food) supply. Such plasticity seems likely to minimize predation risk during the vulnerable period early in life when individuals are warningly coloured and must make the transition from an undefended phenotype to a mature aposematic state.

The complex processes involved with animal migration have long been a subject of biological interest, and broad-scale movement patterns of many marine turtle populations still remain unresolved. While it is widely accepted that once marine turtles reach sexual maturity they home to natal areas for nesting or reproduction, the role of philopatry to natal areas during other life stages has received less scrutiny, despite widespread evidence across the taxa. Here we report on genetic research that indicates that juvenile hawksbill turtles (Eretmochelys imbricata) in the eastern Pacific Ocean use foraging grounds in the region of their natal beaches, a pattern we term natal foraging philopatry. Our findings confirm that traditional views of natal homing solely for reproduction are incomplete and that many marine turtle species exhibit philopatry to natal areas to forage. Our results have important implications for life-history research and conservation of marine turtles and may extend to other wide-ranging marine vertebrates that demonstrate natal philopatry.

During early development, many aposematic species have bright and conspicuous warning appearance, but have yet to acquire chemical defenses, a phenotypic state which presumably makes them vulnerable to predation. Body size and signal luminance in particular are known to be sensitive to variation in early nutrition. However, the relative importance of these traits as determinants of predation risk in juveniles is not known. To address this question, we utilized computer‐assisted design (CAD) and information on putative predator visual sensitivities to produce artificial models of postmetamorphic froglets that varied in terms of body size and signal luminance. We then deployed the artificial models in the field and measured rates of attack by birds and unknown predators. Our results indicate that body size was a significant predictor of artificial prey survival. Rates of attack by bird predators were significantly higher on smaller models. However, predation by birds did not differ between artificial models of varying signal luminance. This suggests that at the completion of metamorphosis, smaller froglets may be at a selective disadvantage, potentially because predators can discern they have relatively low levels of chemical defense compared to larger froglets. There is likely to be a premium on efficient foraging, giving rise to rapid growth and the acquisition of toxins from dietary sources in juvenile poison frogs.