Molecular markers based on mitochondrial (mt) DNA control region sequences 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.

No abstract

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 environments. 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 demography of this endangered species. Ecology, Vol. 84, No. 5 PLATE 1. An oceanic-stage loggerhead with a curved carapace length of 17.3 cm. The sharp projections on the vertebral scutes are characteristic of this life stage. Photograph by Skye White.

Analysis of teleost sagittal otoliths contained in scats has been widely used to determine the diet of seals. This method is based on the assumption that relative frequencies of otoliths in scats faithfully reflect those offish in the diet. This assumption has rarely been tested experimentally. We compared the ratios of herring (Clupea harengus) to sprat (Sprattus sprattus) otoliths in faeces (output) of captive California sea lions (Zalophus californianus) and South American fur seals (Arctocephalus australis) with the ratios at feeding (input). Sea lions and fur seals showed no consistent differences in recovery rates and partial digestion of otoliths. Output ratios deviated only slightly from input ratios, the smaller sprat otoliths being underrepresented in the output by 8%. Only about 40% of the otoliths fed to the seals were found in the scats. For both species partial digestion of otoliths led to a 16% underestimation of fish length and a 35% underestimation of fish mass.

Molecular markers based on mitochondrial (mt) DNA control region sequences 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.

Analysis of fish otoliths in scats and vomits of Galápagos fur seals (Arctocephalus galapagoensis) and Galápagos sea lions (Zalophus californianus wollebaeki) was used to determine the numerical composition of the diets for the post-El Niño year 1983, the cold seasons in 1984 and 1985, and the warm season in 1986. Between 84 and 99% of all otoliths in fur seal scats were from myctophids and bathylagids. The fur seals' diet included 26 species. Only 3 species contributed more than 1% of otoliths. No seasonal differences in diet were found. Sea lion samples contained a mean of 14 otoliths. Sardines (Sardinops sagax) contributed 75-85% of otoliths. Sea lions preyed on 24 species, but only 3 surpassed 1% abundance. Seasonality was not reflected in the sea lions' diet. After the 1982-1983 El Niño, the diets of both species deviated from those in all other years of the study. Food-niche overlap between the two sympatric species was almost non-existent. This is hard to understand, based on our knowledge of the diving capabilities of the two species, but reflects the fact that Galápagos fur seals are nighttime foragers and sea lions are daytime foragers.

Columbus crabs, Planes minutus (Crustacea: Brachyura) live in the open ocean attached to floating substrata including Sargassum, flotsam, and sea turtles. Eighty-two percent of 128 loggerhead turtles (Caretta caretta) checked, harboured a total of 172 crabs. Crabs inhabiting flotsam occurred in mixed sex groups of adults and juveniles, with a mean group size of 8.2 ±;11.8 (N=17). In contrast, crabs living on sea turtles around Madeira occur in smaller groups 1.6 ±0.5 (N=105) which are typically adult heterosexual pairs (61 out of 105). Crabs on turtles were bigger than on flotsam and a higher proportion of female crabs were brooding eggs. Columbus crabs exhibit different life history strategies depending on the substratum they inhabit.

Analysis of fish otoliths in scats and vomits of Galápagos fur seals (Arctocephalus galapagoensis) and Galápagos sea lions (Zalophus californianus wollebaeki) was used to determine the numerical composition of the diets for the post-El Niño year 1983, the cold seasons in 1984 and 1985, and the warm season in 1986. Between 84 and 99% of all otoliths in fur seal scats were from myctophids and bathylagids. The fur seals' diet included 26 species. Only 3 species contributed more than 1% of otoliths. No seasonal differences in diet were found. Sea lion samples contained a mean of 14 otoliths. Sardines (Sardinops sagax) contributed 75-85% of otoliths. Sea lions preyed on 24 species, but only 3 surpassed 1% abundance. Seasonality was not reflected in the sea lions' diet. After the 1982-1983 El Niño, the diets of both species deviated from those in all other years of the study. Food-niche overlap between the two sympatric species was almost non-existent. This is hard to understand, based on our knowledge of the diving capabilities of the two species, but reflects the fact that Galápagos fur seals are nighttime foragers and sea lions are daytime foragers.Résumé : La composition numérique des poissons dans le régime alimentaire a été déterminée par analyse des otolithes contenus dans les fèces et les régurgitations des Otaries de Galápagos (Arctocephalus galapagoensis) et des Lions de mer de Galápagos (Zalophus californianus wollebacki) au cours de l'année post-El Niño, 1983, au cours des saisons froides 1984 et 1985, et au cours de la saison chaude 1986. De 84 à 99% de tous les otolithes contenus dans les fèces des otaries étaient des otolithes de myctophidés et les bathylagidés. Le régime alimentaire des otaries contenait 26 espèces dont seulement trois ont fourni plus de 1% des otolithes. Le régime ne subissait pas de variations saisonnières. Les échantillons provenant des lions de mer contenaient en moyenne 14 otolithes. De 75 à 85% des otolithes étaient des otolithes de Sardines (Sardinops sagax). Les lions de mer se sont nourris de 24 espèces, mais seulement trois d'entre elles ont fourni plus de 1% des otolithes. Il n'y avait pas de variation saisonnière dans le régime alimentaire des lions de mer. Après El Niño, en 1982-83, le régime alimentaire s'est avéré différent de ce qu'il a été au cours de toutes les autres années. Les régimes alimentaires des deux espèces ne se chevauchaient presque pas, ce qui est étonnant si l'on tient compte de leur capacité de plongée, mais qui s'explique si l'on tient compte des habitudes alimentaires nocturnes des otaries et des habitudes alimentaires diurnes des lions de mer.