Estimating demographic parameters for loggerhead sea turtles using mark–recapture data and a multistate model

The survival for adult loggerhead sea turtles from a saturation tagging study on Bald Head Island, NC, USA, was estimated using a multistate model with unobservable states to relax assumptions that are violated when survival is estimated from multistate models and produce more accurate estimates of survival, recapture, and breeding transition probabilities. The influence of time, trap dependence, and low site fidelity to the study nesting beach on survival and recapture were examined. The best model given the data included an imprecise site-fidelity effect on survival, constrained the reproductive cycle to 4 years, and contained a time effect on recapture rates. The estimate of annual survival for adult females was of 0.85, producing the highest estimate in the literature for loggerhead sea turtles. Multistate models should be applied to other nesting beach data for sea turtles to improve survival estimates and in turn the ability to model and manage populations.     

Skeletochronological assessment of age structure and population stability for two threatened frog species

Populations that fluctuate in size may become small at particular times and therefore be at risk of extinction. I used skeletochronology to examine the potential for fluctuations in population size in the threatened frog species Geocrinia alba and Geocrinia vitellina from southwestern Australia. The change in number of lines of arrested growth (LAG) in toe bones of recaptured frogs indicated that most individuals probably gain one LAG annually. Therefore, skeletochronology can be used for age determination. From a combination of skeletochronology and a mark–recapture study, both species appear to live for a maximum of six years. However, the majority of adult males only bred in a single year, which gave rise to a consistently dominant three-year-old age class. A drop in the number of two-year-old frogs and a large increase in the number of three-year-olds (up to 85%) from 1993 to 1994 in both species highlighted the potential for substantial fluctuations in population size. Widespread changes in abundance of between 25 and 50% may therefore be expected over periods as short as one or two years, due to variation in recruitment success.     

Ecological regime shift drives declining growth rates of sea turtles throughout the West Atlantic

Somatic growth is an integrated, individual‐based response to environmental conditions, especially in ectotherms. Growth dynamics of large, mobile animals are particularly useful as bio‐indicators of environmental change at regional scales. We assembled growth rate data from throughout the West Atlantic for green turtles, Chelonia mydas, which are long‐lived, highly migratory, primarily herbivorous mega‐consumers that may migrate over hundreds to thousands of kilometers. Our dataset, the largest ever compiled for sea turtles, has 9690 growth increments from 30 sites from Bermuda to Uruguay from 1973 to 2015. Using generalized additive mixed models, we evaluated covariates that could affect growth rates; body size, diet, and year have significant effects on growth. Growth increases in early years until 1999, then declines by 26% to 2015. The temporal (year) effect is of particular interest because two carnivorous species of sea turtles—hawksbills, Eretmochelys imbricata, and loggerheads, Caretta caretta—exhibited similar significant declines in growth rates starting in 1997 in the West Atlantic, based on previous studies. These synchronous declines in productivity among three sea turtle species across a trophic spectrum provide strong evidence that an ecological regime shift (ERS) in the Atlantic is driving growth dynamics. The ERS resulted from a synergy of the 1997/1998 El Niño Southern Oscillation (ENSO)—the strongest on record—combined with an unprecedented warming rate over the last two to three decades. Further support is provided by the strong correlations between annualized mean growth rates of green turtles and both sea surface temperatures (SST) in the West Atlantic for years of declining growth rates (r = −.94) and the Multivariate ENSO Index (MEI) for all years (r = .74). Granger‐causality analysis also supports the latter finding. We discuss multiple stressors that could reinforce and prolong the effect of the ERS. This study demonstrates the importance of region‐wide collaborations.     

Validation and Application of Skeletochronology for Age Determination of the Ryukyu Ground Gecko,Goniurosaurus kuroiwae （Squamata： Eublepharidae）

Skeletochronology is a method commonly used for estimating the age of amphibians and reptiles in the wild. However, the number of lines of arrested growth （LAGs） does not necessarily reflect age in some species. We validated the applicability of this method to an endangered eublepharid gecko, Goniurosaurus kuroiwae, then inferred its longevity and age structures in wild populations. We classified young geckos into three groups using previously published data for early growth： Group 1 contained hatchlings before the first winter, Group 2 contained hatchlings after the first win- ter, and Group 3 included yearlings after the second winter. LAG numbers in these groups were then compared. All individuals in Group 1 possessed a single LAG, which was considered as a hatching line. Most individuals in Groups 2 and 3 possessed one and two additional LAGs, respectively （LAG1 and LAG2）, corroborating the notion that LAGs are formed annually. A few geckos exhibited fewer LAGs than expected. Analysis of variations in LAG and marrow cavity diameter demonstrated that in animals with fewer LAGs, endosteal resorption or fusion of hatching line and LAG1 had occurred. LAG2 was never lost by endosteal resorption and was identifiable by its diameter. Thus, the age of adult geckos could be determined by counting LAGs outward from LAG2. Application of this method to wild populations re- vealed that the longevity of this species is not less than 83 months, but that almost all individuals in fragmented habitats die before 50 months, suggesting lower population sustainability in such habitats.     

Combining capture–recapture data and known ages allows estimation of age‐dependent survival rates

In many animal populations, demographic parameters such as survival and recruitment vary markedly with age, as do parameters related to sampling, such as capture probability. Failing to account for such variation can result in biased estimates of population‐level rates. However, estimating age‐dependent survival rates can be challenging because ages of individuals are rarely known unless tagging is done at birth. For many species, it is possible to infer age based on size. In capture–recapture studies of such species, it is possible to use a growth model to infer the age at first capture of individuals. We show how to build estimates of age‐dependent survival into a capture–mark–recapture model based on data obtained in a capture–recapture study. We first show how estimates of age based on length increments closely match those based on definitive aging methods. In simulated analyses, we show that both individual ages and age‐dependent survival rates estimated from simulated data closely match true values. With our approach, we are able to estimate the age‐specific apparent survival rates of Murray and trout cod in the Murray River, Australia. Our model structure provides a flexible framework within which to investigate various aspects of how survival varies with age and will have extensions within a wide range of ecological studies of animals where age can be estimated based on size.     

A skeletochronological study of age and growth in relation to adult size in the water frog Rana epeirotica

The age and growth of individuals in a population of the water frog Rana epeirotica, from northwestern Greece, were studied in 1998 and 1999 using skeletochronology. Analysis of the age structure was based on the enumeration of Lines of Arrested Growth (LAGs) in phalanges. Ages ranged from 1-5 years among 145 males and from 1-5 years among 173 females. The mean snout-vent length was 72.74 +/- 7.96 mm in males and 83.63 +/- 11.73 mm in females. The difference between the sexes in age and size was significant. Endosteal resorption may have eroded away the first LAG in only 9% of the studied individuals and was more frequent in females. Growth of adults was fitted by the Bertalanffy model. The growth coefficient (K) was 0.88 in males and 0.49 in females, reflecting faster male growth between metamorphosis and maturation.     

Mixed-stock aging analysis reveals variable sea turtle maturity rates in a recovering population

Quantifying demographic parameters and variable vital rates, such as somatic growth rates, time to maturity, and reproductive longevity, is important for effective management of threatened and endangered populations such as sea turtles (Cheloniidae). To address these knowledge gaps, we applied skeletochronology to analyze and compare somatic growth rates and variation in life-history traits such as age and size at sexual maturity for 65 green turtles (Chelonia mydas) in the eastern Pacific Ocean (EP), along the west coast of the United States; turtles belonged to ≥2 nesting subpopulations that differed in body size (mean nesting size). Green turtles in the EP spend approximately 5 years in the oceanic stage before recruiting to nearshore habitats, males may be smaller and younger than females at maturation (x̅ = 17.7 ± 5.5 yr vs. 28.0 ± 8.2 yr), and younger age at sexual maturity was associated with smaller size at sexual maturity, suggesting that mean nesting body size may be reflective of maturation timing for subpopulations. Smaller body sizes for females nesting at Michoacán, Mexico (continental) rookeries, yielded a younger predicted age at sexual maturity (x̅ = ~17 yr) compared to females from Revillagigedo Islands, Mexico rookeries, which displayed larger body sizes and older age at sexual maturity (x̅ = ~30 yr). We consider possible mechanisms driving the observed divergence in life-history traits, including the possibility that earlier maturation (reduced generation length) for turtles in the Michoacán nesting subpopulation may be a response to intense harvesting in the past 50 years, and consideration of such anthropogenic impacts is warranted by population managers. Finally, our results indicate green turtles moved into nearshore neritic habitats at a young age (4–6 yr), emphasize the importance of protecting neritic habitats along the southwestern United States and northwestern Mexican coasts, and encourage the incorporation of variable maturation time in population recovery assessments.     

A potential contamination error associated with insect protein mark‐capture data

Various types of protein‐spray solutions have proven effective for externally tagging arthropods for mark‐release‐recapture and mark‐capture type dispersal research. However, there is concern that certain standardized arthropod collection methods, such as sweep netting, might lead to high incidences of protein transfer from field‐marked to unmarked arthropods during sample collection and sample handling. Native arthropods were collected in sweep nets from a field of alfalfa, Medicago sativa L. (Fabaceae). The nets also contained 10 egg white‐, 10 bovine milk‐, 10 soy milk‐, and 10 water (control)‐marked Hippodamia convergens Guérin‐Méneville (Coleoptera: Coccinellidae) that were visually distinguishable by a yellow, white, green, and blue dot, respectively. The plant debris and arthropods from each sweep net collection were then placed into either a paper or a plastic bag and frozen for storage. The contents of each sweep net sample were thawed and the color‐coded H. convergens and field‐collected arthropods were examined for the presence of each protein by an egg white (albumin), bovine milk (casein), and soy milk (soy trypsin) enzyme‐linked immunosorbent assay (ELISA). Data revealed that only 0.67, 0.81, and 0% of the field‐collected unmarked arthropods acquired an egg white, bovine milk, and soy milk mark, respectively. ELISA results also showed that all the egg white‐marked H. convergens retained their mark, but 22.1% of the bovine milk‐marked and 5.1% of the soy milk‐marked H. convergens (color‐coded beetles) lost their mark during the collection and sample handling processes.     

A skeletochronological study on a subtropical, riparian ranid (Rana swinhoana) from different elevations in Taiwan

We estimated the age, longevity, and growth patterns of a subtropical ranid, Rana swinhoana from high (Lishing) and low (Wulai) elevations using skeletochronology. In addition, we also measured body mass and length of frogs from five other localities. Results showed that both snout-vent length and body mass of frogs were significantly correlated with altitudes for both sexes. Frogs of Lishing were significantly larger and older than that of Wulai. We used LAGs to estimate the age and growth of frogs and found that the growth of Wulai frog of both sexes slowed down at an earlier age than that of Lishing frogs. Male and female frogs from Wulai did not exceed 6 and 7 years, respectively, while the maximum age of males and females of Lishing was 7 and 11 years, respectively. Results suggest that the LAGs observed in R. swinhoana correspond to low temperature and/or decreased food availability instead of desiccation during the harsh annual period (November to February). Skeletochronological data suggest that the variations of body size of R. swinhoana among elevations are likely associated with the growth, age at sexual maturity, and longevity.     

Bioko: critically important nesting habitat for sea turtles of West Africa

We evaluate the conservation status and threats faced by sea turtle nesting populations at Bioko Island, Equatorial Guinea (Central Africa). Beaches were monitored to obtain a detailed sea turtle nest census and, where possible, tagging of adult females was undertaken. Four sea turtle species were found nesting in the area: the green turtle (Chelonia mydas), the leatherback (Dermochelys coriacea), the olive ridley (Lepidochelys olivacea) and the hawksbill (Eretmochelys imbricata); with the former two species nesting in regionally important numbers. Nesting activity was concentrated between November and February, with a peak in December–January. Tagging and recapture of green turtles in two consecutive seasons suggested an estimated 560 (interquartile range: 420–1,681) and 414 (interquartile range: 190–1,255) nesting females in the area, respectively. Estimated numbers of nesting leatherbacks ranged from 123 to 215 and 243 to 293 in the first and second season, respectively. The other two species were less abundant (olive ridley: 19–29 and 28–43; hawksbill: 4–10 and 2 turtles). Data were compared with more recent surveys in the area and contextualised with information on human related threats. Despite the size of nesting stocks, ongoing permitted and illegal take of adult turtles at the nesting site constitutes a serious threat for these breeding aggregations. Additionally, tag returns from throughout the Gulf of Guinea suggest that the level of take in regional fisheries may also be a major threat.     

Insights into vertebral band pair deposition rate in the juvenile common thresher shark (Alopias vulpinus) in the northeastern Pacific Ocean

Validation of band pair deposition rates in elasmobranch vertebrae is essential for accurate age estimation using band pair counting techniques. We present a validation study of the vertebral band pair deposition rate for juvenile common thresher sharks Alopias vulpinus in the northeastern Pacific Ocean (NEPO) using tag and recapture with oxytetracycline (OTC) injection. A total of 14 juvenile A. vulpinus marked with OTC from 1998 through 2013 were recaptured with times at liberty ranging from 1.08 to 3.81 years with an average of 2.14 years (±0.97 years standard deviation, SD). Shark size ranged from 80 to 128 cm fork length (LF) at the time of OTC injection and from 112 to 168 cm LF for those measured at recapture. The slopes of the relationships between band pairs post OTC and years at liberty for each reader ranged from 0.84 to 0.95, slightly lower than the 1.0 slope expected from annual band pair formation. These findings preliminarily support previous age and growth assumptions based on a one band pair per year deposition rate. However, high variation in band pair deposition rates between samples, coupled with regression slopes falling just under one band pair per year, indicates that further investigation is needed to refine band pair deposition rate estimates.     

Structure of the femora and autotomous (postpygal) caudal vertebrae in the three-toed skink Chalcides chalcides (Reptilia: Squamata: Scincidae) and its applicability for age and growth rate determination

The limbs of the three-toed skink Chalcides chalcides are reduced to such a degree that the three digits are too small for skeletochronology. This study, performed on animals collected near Isernia (central Italy), describes the structure of the caudal vertebrae, which are often naturally lost due to autotomy, in order to determine whether they can be used to obtain data on age and growth with skeletochronological techniques. The reliability of the autotomous caudal vertebrae for skeletochronology was verified by performing skeletochronological analyses also on femora. Although the identification of the lines of arrested growth (LAGs) was easier in femora than in autotomous caudal vertebrae, a high correspondence of the LAG count between the two bones was observed. Females were larger and lived longer than males (4 and 3 years, respectively). For both sexes, the snout vent length (SVL) was significantly correlated with age. For both sexes, sexual maturity was attained after two hibernations from birth, beginning at the 20th month of age. At first reproduction, males had an SVL of 91–106 mm and females one of 111–150 mm. Von Bertalanffy growth curves of age versus SVL showed that females had slower growth rates than males for attaining their asymptotic SVL (females: 197 mm; males: 143 mm). The results provide the first data on age and growth of C. chalcide, and show that autotomous caudal vertebrae are reliable alternatives for obtaining such data for limb-reduced reptiles, avoiding the need to sacrifice or disable animals, as occurs when long bones are used.     

Site fidelity of intertidal fish to rockpools

Gobius paganellus, Lipophrys pholis and Coryphoblennius galerita are wide‐spread intertidal fish that spend their earlier life stages in rock pools, and yet very little is known about their site fidelity behaviour. For these species, fidelity to rockpools may result in increased fitness costs in a predicted scenario of warmer sea water, due to the low thermal inertia of these water bodies. In this context, it is relevant to investigate these species' site fidelity. We made a mark‐recapture study to assess the mentioned species' movements within and between rockpools. We tagged a total of 530 individuals of the aforementioned species with the Visible Implant Elastomer and tracked their movement for a 7‐month period. We found that site fidelity and specific rockpools conditions are important factors in distribution of intertidal blennies and gobies. We also examined the relations between rockpool volume, depth and site fidelity. We found that G. paganellus tends to remain in its original marking pool, with an average recapture rate of 20.5%, but showed no evidence of inter‐pool movement. Rockpool depth, however, proved to be important in the blennies' movements. Our findings are among the first to prove that a mark‐recapture method can be successfully used to track intertidal fish movements. In particular, we showed that G. paganellus presents site fidelity in intertidal rockpools during its early ontogeny for a period of two to three months.     

Age‐ and sex‐specific survival of California sea lions (Zalophus californianus) at San Miguel Island,California

We conducted a mark‐recapture study of California sea lions (Zalophus californianus) using pups branded on San Miguel Island, California, from 1987 to 2014, and annual resightings from 1990 to 2015. We used the Burnham model (Burnham 1993), an extension of the Cormack‐Jolly‐Seber mark‐recapture model, which includes recoveries of dead animals, to analyze age, sex, and annual patterns in survival. Generally, females had higher survival than males. For female pups, the average annual survival was 0.600 and for male pups it was 0.574. Yearling survival was 0.758 and 0.757 for females and males, respectively. Peak annual survival was at age 5 and was 0.952 for females and 0.931 for males. Pups with larger mass at branding had higher survival as pups and yearlings, but the effect was relative within each cohort because of large between‐cohort variability in survival. Annual variability in sea surface temperature (SST) affected survival. For each 1°C increase in SST, the odds of survival decreased by nearly 50% for pups and yearlings; negative SST anomalies yielded higher survival. Annual variation in male survival was partly explained by leptospirosis outbreaks. Our study provides a unique view of one demographic parameter that contributed to the successful recovery of the California sea lion population.     

Large-scale use of fish traps for monitoring sea trout (Salmo trutta) smolts and sea lice (Lepeophtheirus salmonis) infestations: efficiency and reliability

Lice-infected sea trout populations were monitored using fish traps in the Romsdalsfjord (Norway). The reliability and efficiency of this capture technique, which allows estimation of lice infestation rates without killing the fish, was evaluated through a mark–recapture study. A total of 2447 sea trout smolts were captured, tagged and released over a three-year period. There was a considerable variation in capture rates (range: 0.4–17.7 fish per day) and sea lice numbers (number of lice per fish: 2.8–30.3; number of lice per gram body weight: 0.02–0.69) among localities, sampling times and years. Recapture rates of tagged fish with traps, which were low (2% or 0.11 fish per day), showed that the risk for pseudoreplication was minor, in terms of counting lice on the same fish several times. Most of the tagged sea trout (90%) were recaptured within the first two months after release, and no significant variations in lice numbers were found between tagging and recapture. The lack of differences in lice levels between tagging and recapture during the first week after tagging indicated that the method most likely would not significantly underestimate the lice infestations due to loss of lice during handling. Therefore, our results confirm that the use of fish traps is a suitable method for estimation of lice numbers on wild salmonids.     

Laying date,body mass and tick infestation of nestling tropical Roseate Terns Sterna dougallii predict fledging success,first‐year survival and age at first return to the natal colony

Both intrinsic and extrinsic factors recorded at individual nests can predict offspring fitness and survival but few studies have examined these effects in the tropics. We recorded nestling survival, post‐fledging survival and age at first return of Roseate Terns breeding at Aride Island, Seychelles, over a 12‐year period (1998–2009). Nest data recorded at the egg, nestling and fledging stages were collected during six breeding seasons (1998, 2001–2005) and a capture‐mark‐recapture dataset of six cohorts of fledglings was obtained from 2001–2009. Logistic regression models were used to assess the predictive effect of reproductive variables on fledging success, while multistate capture‐mark‐recapture models were used to estimate post‐fledging survival and return–recruitment probabilities to the natal site. Nestling survival probability increased with earliness of laying and was negatively affected by tick infestation during the growth period (0–23 days). Fledging probability was also positively related to chick body condition, whereas other pre‐fledging reproductive parameters such as clutch size and egg size were not influential. A multistate modelling of age‐specific survival and return–recruitment (transition) rates found that first‐year survival differed between cohorts and was also negatively affected by tick infestation. Annual survival stabilized from age 2 onwards at 0.83 ± 0.02. Transition rates were positively related to body condition at fledging, with heavier individuals returning for the first time to the natal colony at a younger age compared with lighter individuals. These results highlight the importance of local conditions encountered by tropical seabirds during the breeding season in shaping demographic parameters.     

Bone histology as an approach to providing data on certain key life history traits in mammals: Implications for conservation biology

The knowledge of the life histories of wild mammals is of crucial importance in the field of conservation management. The endangered status of many species calls for faster data collection that can be used in risk assessment and, ultimately, for designing conservation policies. This study is pioneering the potential of bone histology to provide data on life history traits crucial for conservation biology in long-lived mammals. Long bone cross-sections show pronounced annual cycles of growth arrest allowing application of skeletochronology (counts of lines of arrested growth ‘LAGs’). Consequently, the number of LAGs within the primary fast-growing bone tissue up to the outer cortical slow-growing bone tissue corresponds to the age at first reproduction; whereas the age at death can be estimated by the total number of rest lines throughout the whole of bone cross-section. Furthermore, the diameters of successive growth rings as well as the osteocyte lacuna density may shed light on growth rates. We use the endangered desert dwelling antelope Addax nasomaculatus as a case study. By analyzing different ontogenetic stages in five Addax individuals (three captive and two wild specimens) from a museum collection, we show that bone histology may be a reliable tool for determining certain key life history traits. In our sample, the wild Addax female attained reproductive maturity at three years, whereas the male specimens, both the captive and the wild ones, reached maturity at four years. This is congruent with data from other large antelopes with male-biased size dimorphism, but differs slightly from data on sexual maturity previously published for wild Addax. Moreover, quantification of osteocyte lacunae in both adult males provides a higher cell density in the captive one than in the wild one suggesting the strong effect of constant resources supply in individuals from zoos on growth rates. While age at first reproduction and longevity are essentials parameters to carry out demographic models, growth rates may allow evaluation of the health status of wild populations. This approach may provide useful data on life history traits when applied to bones collected in the wild.     

First Assessment of the Sex Ratio for an East Pacific Green Sea Turtle Foraging Aggregation: Validation and Application of a Testosterone ELISA

Determining sex ratios of endangered populations is important for wildlife management, particularly species subject to sex-specific threats or that exhibit temperature-dependent sex determination. Sea turtle sex is determined by incubation temperature and individuals lack external sex-based traits until sexual maturity. Previous research utilized serum/plasma testosterone radioimmunoassays (RIA) to determine sex in immature/juvenile sea turtles. However, there has been a growing application of enzyme-linked immunosorbent assay (ELISA) for wildlife endocrinology studies, but no study on sea turtles has compared the results of ELISA and RIA. This study provides the first sex ratio for a threatened East Pacific green sea turtle (Chelonia mydas) foraging aggregation, a critical step for future management of this species. Here, we validate a testosterone ELISA and compare results between RIA and ELISA of duplicate samples. The ELISA demonstrated excellent correspondence with the RIA for providing testosterone concentrations for sex determination. Neither assay proved reliable for predicting the sex of reproductively active females with increased testosterone production. We then applied ELISA to examine the sex ratio of 69 green turtles foraging in San Diego Bay, California. Of 45 immature turtles sampled, sex could not be determined for three turtles because testosterone concentrations fell between the ranges for either sex (females: 4.1–113.1 pg/mL, males: 198.4–2,613.0 pg/mL) and these turtles were not subsequently recaptured to enable sex determination; using a Bayesian model to predict probabilities of turtle sex we predicted all three ‘unknowns’ were female (> 0.86). Additionally, the model assigned all turtles with their correct sex (if determined at recapture) with 100% accuracy. Results indicated a female bias (2.83F:1M) among all turtles in the aggregation; when focusing only on putative immature turtles the sex ratio was 3.5F:1M. With appropriate validation, ELISA sexing could be applied to other sea turtle species, and serve as a crucial conservation tool.     

Skeletochronological estimation of age and growth of loggerhead sea turtles (Caretta caretta) in the western South Atlantic Ocean

Age and growth are important parameters for better understanding of life history and population dynamics of animal species, as well as for formulating management strategies. However, these data are difficult to obtain for sea turtles because of overall slow growth, delayed maturation and highly migratory behaviour. The loggerhead sea turtle, Caretta caretta, is a widely distributed species, globally listed as endangered. Although the species has been well‐studied in some regions, little is known about various aspects of its biology in other populations, such as those in the waters of the western South Atlantic Ocean, especially outside nesting areas. To address age and growth, loggerhead turtles found dead stranded on the northern coast of the state of Rio Grande do Sul during a period of 16 years (1994–2010) were utilized for estimation of age and growth rates using skeletochronology. The individuals analyzed were predominantly neritic juveniles, ranging from 53 to 101 cm curved carapace length (CCL; mean = 71 cm), with estimated ages between 10 and 29 years (mean = 15 years). Mean estimated annual growth rate was 2.1 cm CCL year^?1 (1.9 cm SCL yr^?1), showing large variation among individuals and between successive years in the same individual. Generalized additive mixed models analysis indicated that growth response was influenced by age, CCL and year. The results demonstrated that the southern coast of Brazil is an important area for the development of neritic juveniles of this species, which appear to recruit to this region beginning at about 12 years of age and sizes greater than 55 cm CCL.     

High rates of growth recorded for hawksbill sea turtles in Anegada,British Virgin Islands

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.