Cause-specific temporal and spatial trends in green sea turtle strandings in the Hawaiian Archipelago (1982–2003)

We investigated cause-specific temporal and spatial trends in sea turtle strandings in the Hawaiian Archipelago. Five species of sea turtle were recorded in 3,861 strandings over a 22-year period (1982–2003). Green turtles comprised 97% of these strandings with size and gender composition reflecting the demographic structure of the resident green turtle population and relative green turtle abundance in Hawaiian waters. The cause of strandings was determined by necropsy based on a complete gross external and internal examination. Totally 75% of the 3,732 green turtle strandings were from Oahu where strandings occur year-round. The most common known cause of the green turtle strandings was the tumour-forming disease, fibropapillomatosis (28%) followed by hook-and-line fishing gear-induced trauma (7%), gillnet fishing gear-induced trauma (5%), boat strike (2.5%), and shark attack (2.7%). Miscellaneous causes comprised 5.4% of strandings whereas 49% of green turtle strandings could not be attributed to any known cause. Green turtle strandings attributable to boat strike were more likely from Kauai and Oahu while fibropapilloma strandings were more likely from Oahu and Maui. Hook-and-line gear strandings were more likely from Oahu due to higher per capita inshore fishing effort. The specific mortality rate (conditional probability) for fibropapillomatosis was 88%, 69% for gillnet gear and 52% for hook-and-line gear. The probability of a dead green turtle stranding increased from 1982 but levelled off by the mid-1990s. The declining mortality risk was because the prevalence and severity of fibropapillomatosis has decreased recently and so has the mortality risk attributable to gillnet gear. Despite exposure to disease and inshore fishing gears, the Hawaiian green turtle stock continues to recover following protection since the late 1970s. Nevertheless, measures to reduce incidental capture of sea turtles in coastal Hawaiian fisheries would be prudent, especially since strandings attributable to hook-and-line fishing gear have increased steadily since 1982.     

Spatial and temporal variability in somatic growth of green sea turtles (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) resident in the Hawaiian Archipelago

The somatic growth dynamics of green turtles (Chelonia mydas) resident in five separate foraging grounds within the Hawaiian Archipelago were assessed using a robust non-parametric regression modelling approach. The foraging grounds range from coral reef habitats at the north-western end of the archipelago, to coastal habitats around the main islands at the south-eastern end of the archipelago. Pelagic juveniles recruit to these neritic foraging grounds from ca. 35 cm SCL or 5 kg (~6 years of age), but grow at foraging-ground-specific rates, which results in quite different size- and age-specific growth rate functions. Growth rates were estimated for the five populations as change in straight carapace length (cm SCL year^–1) and, for two of the populations, also as change in body mass (kg year^–1). Expected growth rates varied from ca. 0–2.5 cm SCL year^–1, depending on the foraging-ground population, which is indicative of slow growth and decades to sexual maturity, since expected size of first-time nesters is 80 cm SCL. The expected size-specific growth rate functions for four populations sampled in the south-eastern archipelago displayed a non-monotonic function, with an immature growth spurt at ca. 50–53 cm SCL (~18–23 kg) or ca. 13–19 years of age. The growth spurt for the Midway atoll population in the north-western archipelago occurs at a much larger size (ca. 65 cm SCL or 36 kg), because of slower immature growth rates that might be due to a limited food stock and cooler sea surface temperature. Expected age-at-maturity was estimated to be ca. 35–40 years for the four populations sampled at the south-eastern end of the archipelago, but it might well be >50 years for the Midway population. The Hawaiian stock comprises mainly the same mtDNA haplotype, with no differences in mtDNA stock composition between foraging-ground populations, so that the geographic variability in somatic growth rates within the archipelago is more likely due to local environmental factors rather than genetic factors. Significant temporal variability was also evident, with expected growth rates declining over the last 10–20 years, while green turtle abundance within the archipelago has increased significantly since the mid-1970s. This inverse relationship between somatic growth rates and population abundance suggests a density-dependent effect on somatic growth dynamics that has also been reported recently for a Caribbean green turtle stock. The Hawaiian green turtle stock is characterised by slow growth rates displaying significant spatial and temporal variation and an immature growth spurt. This is consistent with similar findings for a Great Barrier Reef green turtle stock that also comprises many foraging-ground populations spanning a wide geographic range.Communicated by P.W. Sammarco, Chauvin     

Delayed ontogenic dietary shift and high levels of omnivory in green turtles (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) from the NW coast of Africa

Young green turtles (Chelonia mydas) spend their early lives as oceanic omnivores with a prevalence of animal prey. Once they settle into neritic habitats (recruitment), they are thought to shift rapidly to an herbivorous diet, as revealed by studies in the Greater Caribbean. However, the precise timing of the ontogenic dietary shift and the actual relevance of animal prey in the diet of neritic green turtles are poorly known elsewhere. Stable isotopes of carbon, sulfur and nitrogen in the carapace scutes of 19 green turtles from Mauritania (NW Africa), ranging from 26 to 102 cm in curved carapace length (CCLmin), were analyzed to test the hypothesis of a rapid dietary shift after recruitment. Although the length of residence time in neritic habitats increased with turtle length, as revealed by a significant correlation between turtle length and the δ¹³C and the δ³⁴S of the scutes, comparison of the δ¹⁵N of the innermost and outermost layers of carapace scutes demonstrated that consumption of macrophytes did not always start immediately after recruitment, and turtles often resumed an animal-based diet after starting to graze on seagrasses. As a consequence, seagrass consumption did not increase gradually with turtle size and animal prey largely contributed to the diet of turtles within the range 29–59 cm CCLmin (76–99% of assimilated nutrients). Seagrass consumption by turtles larger than 59 cm CCLmin was higher, but they still relied largely on animal prey (53–76% of assimilated nutrients). Thus, throughout most of their neritic juvenile life, green turtles from NW Africa would be better classified as omnivores rather than herbivores. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Abundance and survival rates of green turtles in an urban environment: coexistence of humans and an endangered species

Longitudinal capture-mark-recapture data were used to estimate abundance and survival rates for green turtles (Chelonia mydas) in San Diego Bay, California, USA. These turtles were closely associated with warm effluent from a power plant during winter months. The life stage distribution of green turtles in the bay ranged from post-pelagic juveniles to adults (44.0–110.4 cm straight carapace length). During 99 capture sessions between December 2, 1990, and March 25, 2009, 96 individual green turtles were caught. To estimate abundance and survival rates, robust-design mark-recapture models were fitted to capture-recapture histories using software MARK. The estimated annual survival rate was 0.861 (SE = 0.147, 95% CI = 0.356–0.986), whereas annual abundance ranged from 16 (SE = 6.3, 95% CI = 4–29) to 61 (SE = 13.2, 95% CI = 36–88). This study provides the first survival rate and abundance estimates for a green turtle foraging population in the highly industrialized San Diego Bay.     

Age and growth rates of Hawaiian hawksbill turtles (Eretmochelys imbricata) using skeletochronology

The Hawaiian hawksbill population has fewer than 20 females nesting per year; hence, there is a need to monitor this population closely and basic biological information on individual growth and age to maturity is critical. We present a skeletochronology analysis of Hawaiian hawksbills using humeri recovered from 30 dead stranded hawksbills, plus 10 dead hatchlings. Growth mark morphology shows readily distinguishable marks similar in appearance to other species, though some animals displayed more diffuse marks. Growth rates remained high (average 2.24–4.77 cm year^?1) from 20 to 80 cm straight carapace length (SCL). Hawksbills larger than 80 cm SCL had average growth rates of 0.3 cm year^?1. There were few adult turtles in the sample; however, results indicate hawksbills have faster growth rates than loggerhead or green turtles, with probable average age to maturity (at size 78.6 cm SCL) occurring between 17 and 22 years.     

The stomach contents of post-hatchling green and loggerhead sea turtles in the southwest Pacific: an insight into habitat association

Dietary information obtained from stomach contents can provide a wealth of information on an animal’s ecology. Where animals are cryptic, such as the post-hatchling life history stage of a sea turtle, the ecological insight that dietary analyses can provide, may be otherwise unobtainable. Investigations into post-hatchling turtle stomach contents have found planktonic organisms, dominated by pelagic molluscs and crustaceans, hydrozoans, Sargassum and fish eggs. The nature of these dietary organisms provides evidence for the widely accepted hypothesis that, with the exception of the flatback turtle (Natator depressus), the post-hatchling stage of a sea turtle’s life history is pelagic and oceanic. As the majority of studies that have investigated the stomach contents of post-hatchling sea turtles have been conducted on loggerhead turtles (Caretta caretta) in the northern Atlantic and Pacific Oceans, insight derived from dietary investigations into post-hatchling ecology is biased. This study investigates the diet of post-hatchling green turtles (Chelonia mydas) and loggerhead turtles in the southwest Pacific Ocean. Stomach contents were obtained from 55 green and loggerhead post-hatchling turtles that had stranded or been consumed by Coryphaena hippurus. Our findings demonstrate that loggerhead and green post-hatchlings in the southwest Pacific share similar feeding ecology and feed on a variety of neustonic items that are indicative of an oceanic and pelagic existence. The dietary items consumed by both species investigated belong to similar taxonomic groups as those found in previous studies with species level distinctions occurring owing to the different geographical location.     

The relationship between loggerhead turtle (<Emphasis Type="Italic">Caretta caretta</Emphasis>) movement patterns and Mediterranean currents

Previous studies have shown that loggerhead sea turtles (Caretta caretta), monitored by satellite telemetry, complete long-distance migration between the western and eastern Mediterranean basins following a seasonal pattern. This study investigated if these migration routes may be influenced by surface currents by superimposing the tracks of three loggerhead turtles (curved carapace length >55 cm), migrating from the western to the eastern Mediterranean basin, on Lagrangian data of current developed into pseudo-eulerian speed fields. The average travel speed of the turtles was 1.6 km h⁻¹ and did not depend on the current speed or direction. We observed a connection between surface currents and the turtles’ migration routes, although not a conclusive one. These observations show that neritic stage loggerhead turtles conduct migration in two distinct alternate phases: the first characterized by high and constant speed of travel both when swimming with or against currents and the second typified by low travel speeds and a good concurrence between the trailed routes and the course of the currents. These two phases corresponded to two types of movements, one where the turtle migrates actively to reach a specific destination (either neritic foraging, wintering or nesting ground) and the other, where the turtle drifts with the mesoscale current and forages pelagically. It seemed thus, that the influence of currents on a turtle’s movements depends on the turtle’s momentary behaviour and location of residence.     

Comparative skeletochronological analysis of Kemp’s ridley (<Emphasis Type="Italic">Lepidochelys kempii</Emphasis>) and loggerhead (<Emphasis Type="Italic">Caretta caretta</Emphasis>) humeri and scleral ossicles

Skeletochronological analysis of Kemp’s ridley (Lepidochelys kempii) and loggerhead (Caretta caretta) sea turtle humeri and scleral ossicles was conducted to (1) describe the characteristics of scleral ossicles in these species, (2) determine whether the scleral ossicles contain annually deposited skeletal growth marks and (3) evaluate the potential for skeletochronological analysis of ossicles to obtain age data for size classes and species of sea turtles whose humeri exhibit prohibitive amounts of growth mark resorption. Humeri, entire eyes, and/or individual scleral ossicles were collected from stranded, dead sea turtles that were found along the coasts of Florida, North Carolina, Virginia, and Texas, USA. Samples were taken from a total of 77 neritic, juvenile Kemp’s ridleys ranging from 21.1 to 56.8 cm straightline carapace length (SCL), as well as two Kemp’s ridley hatchlings. For loggerheads, samples were obtained from 65 neritic juvenile and adult turtles ranging from 44.7 to 103.6 cm SCL and ten hatchlings. Examination of the ossicles revealed the presence of marks similar in appearance to those found in humeri. The number of marks in the ossicles and humeri of individual juvenile Kemp’s ridleys for which both structures were collected (n = 55) was equivalent, strongly indicating that the marks are annual. However, in large juvenile and adult loggerhead turtles (n = 65), some significant resorption of early growth marks was observed, suggesting that although ossicles might be useful for skeletochronological analysis of small juveniles, they may not provide a reasonable alternative to humeri for obtaining age estimates for older loggerhead sea turtles.     

Temporal, spatial, and body size effects on growth rates of loggerhead sea turtles (Caretta caretta) in the Northwest Atlantic

In response to a call from the US National Research Council for research programs to combine their data to improve sea turtle population assessments, we analyzed somatic growth data for Northwest Atlantic (NWA) loggerhead sea turtles (Caretta caretta) from 10 research programs. We assessed growth dynamics over wide ranges of geography (9–33°N latitude), time (1978–2012), and body size (35.4–103.3 cm carapace length). Generalized additive models revealed significant spatial and temporal variation in growth rates and a significant decline in growth rates with increasing body size. Growth was more rapid in waters south of the USA (<24°N) than in USA waters. Growth dynamics in southern waters in the NWA need more study because sample size was small. Within USA waters, the significant spatial effect in growth rates of immature loggerheads did not exhibit a consistent latitudinal trend. Growth rates declined significantly from 1997 through 2007 and then leveled off or increased. During this same interval, annual nest counts in Florida declined by 43 % (Witherington et al. in Ecol Appl 19:30–54, 2009) before rebounding. Whether these simultaneous declines reflect responses in productivity to a common environmental change should be explored to determine whether somatic growth rates can help interpret population trends based on annual counts of nests or nesting females. Because of the significant spatial and temporal variation in growth rates, population models of NWA loggerheads should avoid employing growth data from restricted spatial or temporal coverage to calculate demographic metrics such as age at sexual maturity.     

Breeding biology of the green turtle,Chelonia mydas, (Reptilia: Cheloniidae) on Wan-An Island,Peng-Hu Archipelago,Taiwan. I. Nesting ecology

The nesting season of the green turtle, Chelonia mydas on Wan-An Island, Peng-Hu Archipelago, Taiwan extended from early June to early October in both 1992 and 1993. Turtles nested on 9 of the 11 beaches on the island. The average inter-nesting interval was 14.9 d. A close relationship between the first reemergence time and the tidal cycle was found in the present study. The mean straight carapace length of the adult female was 96.6 cm. Female turtles produced from one to nine egg clutches; the average clutch size was 113 eggs. The mean egg size was 46.9 mm in diameter and 22.7 g in weight. The average incubation period was 49.3 d. The sediment characteristics of the beaches on the island are well within the incubation requirements for green turtle nesting. The average hatching success was 70%, but was lower in the artificial nest. The average size for hatchlings was 46.9 mm in straight carapace length and 22.7 g in body weight. The health of the hatchling is influenced by the adult female size, the nesting depth and the precipitation during incubation.     

A Contemporary,Sex‐Limited Change in Body Size of an Estuarine Turtle in Response to Commercial Fishing

Abstract: Juvenile growth rate and adult body size are important components of life‐history strategies because of their direct impact on fitness. The diamondback terrapin (Malaclemys terrapin) is a sexually dimorphic, long‐lived turtle inhabiting brackish waters throughout the Atlantic and Gulf coasts of the United States. In parts of its range, terrapins face anthropogenically imposed mortality: juveniles of both sexes inadvertently enter commercial crab traps and drown. For adult females, the carapace eventually grows large enough that they cannot enter traps, whereas males almost never reach that critical size. We compared age structure, carapace dimensions, growth curves, and indices of sexual dimorphism for a Chesapeake Bay population of terrapins (where mortality of turtles is high due to crab traps) with contemporary terrapins from Long Island Sound and museum specimens from Chesapeake Bay (neither group subject to commercial crab traps). We also calculated the allochronic and synchronic rates of evolutionary change (haldanes) for males and females to measure the rate of trait change in a population or between populations, respectively. We found a dramatic shift to a younger male age structure, a decrease in the length of time to terminal female carapace size, a 15% increase in female carapace width, and an increase in sexual dimorphism in Chesapeake Bay. In a new twist, our results implicate a fishery in the selective increase in size of a reptilian bycatch species. These sex‐specific changes in life history and demography have implications for population viability that need to be considered when addressing conservation of this threatened turtle.     

Estimates of sex- and age-class-specific survival probabilities for a southern Great Barrier Reef green sea turtle population

Sex- and age-class-specific survival probabilities of a southern Great Barrier Reef green sea turtle population were estimated using a capture–mark–recapture (CMR) study and a Cormack–Jolly–Seber (CJS) modelling approach. The CMR history profiles for 954 individual turtles tagged over a 9-year period (1984–1992) were classified into three age classes (adult, subadult, juvenile) based on somatic growth and reproductive traits. Reduced-parameter CJS models, accounting for constant survival and time-specific recapture, fitted best for all age classes. There were no significant sex-specific differences in either survival or recapture probabilities for any age class. Mean annual adult survival was estimated at 0.9482 (95% CI: 0.92–0.98) and was significantly higher than survival for either subadults or juveniles. Mean annual subadult survival was 0.8474 (95% CI: 0.79–0.91), which was not significantly different from mean annual juvenile survival estimated at 0.8804 (95% CI: 0.84–0.93). The time-specific adult recapture probabilities were a function of sampling effort but this was not the case for either juveniles or subadults. The sampling effort effect was accounted for explicitly in the estimation of adult survival and recapture probabilities. These are the first comprehensive sex- and age-class-specific survival and recapture probability estimates for a green sea turtle population derived from a long-term CMR program.Communicated by M.S. Johnson, Crawley     

Assessment of non-invasive techniques for monitoring mercury concentrations in species of Amazon turtles

This study determined the concentrations of mercury (Hg) in four tissues of six species of turtles from the Rio Negro in the Amazon Basin. For two species, blood and carapace tissues were correlated with concentrations in internal tissues to establish whether blood or carapace could serve as a non-lethal indicator of internal metal exposure or body burden. The four tissues’ Hg levels were also correlated to turtle size and gender. The liver in five species of turtles had the highest concentration, followed by carapace, muscle, and blood. The exception was Chelus fimbriatus, which had a higher metal concentration in the muscle than carapace. Regarding the correlation between total Hg concentrations in tissues of the two species, no significant correlation was noted for Podocnemis erythrocephala. However, for Podocnemis sextuberculata significant correlation was found between muscle?×?liver, muscle?×?blood, and liver?×?blood. For P. erythrocephala, there was a correlation between Hg concentration in carapace and turtle size. For P. sextuberculata, there was no marked correlation between Hg concentration and size, but concentration in muscle was significantly influenced by gender. The patterns of Hg accumulation in tissues of the five species followed those described for freshwater species and some species of sea turtles. The difference in C. fimbriatus may be a result of a different pattern of non-living keratin layers on the carapace tissue. The use of carapace to infer internal concentrations of Hg is common in freshwater and sea turtles, but in this study it was found that only blood might be a reliable indicator of Hg concentrations in liver and muscle tissues for P. sextuberculata. Thus blood may be used as a non-invasive method to study concentrations of Hg in liver and muscle of P. sextuberculata.     

Patterns in the emergence of green (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) and loggerhead (<Emphasis Type="Italic">Caretta caretta</Emphasis>) turtle hatchlings from their nests

The emergence patterns of both green (Chelonia mydas) and loggerhead (Caretta caretta) turtle hatchlings were observed in great detail over three seasons at Alagadi beach, northern Cyprus. In total, 38 green turtle and 50 loggerhead turtle nests were monitored, accounting for the emergence of 2,807 and 2,259 hatchlings, respectively. We quantified these emergences into 397 green turtle and 302 loggerhead turtle emergence groups. Overall, 85.0% of green turtle and 79.5% of loggerhead turtle groups emerged at night; these accounted for 85.5 and 90.8% of hatchlings, respectively. The remaining emergences were dispersed throughout the day for green turtle nests but confined to the morning in loggerhead turtle nests. Hatchling emergence from individual nests occurred over periods of between 1 and 7 nights, with most hatchlings typically emerging on the first night. Group sizes of green turtles emerging during the day were significantly smaller than those emerging at night. Hatchlings of both species that emerged from nests during the day had longer emergence durations than those that emerged from nests at night only.Communicated by R.J. Thompson, St. Johns     

Post-nesting migrations of green turtles (Chelonia mydas) at Wan-An Island, Penghu Archipelago, Taiwan

 During the summers of 1994 to 1997, eight green turtles (Chelonia mydas) nesting at Wan-An Island, PengHu Archipelago, Taiwan, were equipped with satellite-telemetry transmitters. Using the Argos-linked satellite system, the turtles' migration routes were tracked until the transmissions stopped. The turtles migrated widely on the continental shelf to the east of Mainland China. The migration distances ranged from 193 to 1909 km, and the migration speeds from 1.2 to 2.8 km h⁻¹. The turtles apparently utilize several coastal areas as temporal residential foraging sites, and their migrations consist of both trans-oceanic and coastal legs. The wide distribution of the foraging sites of the turtles comprising this rookery reflects the extent to which the green turtle migrates in northeast Asia; regional and international cooperation will therefore be needed to conserve this declining population. Received: 14 December 1998 / Accepted: 8 May 2000     

Population structure and genetic diversity in green turtles nesting at Tortuguero,Costa Rica,based on mitochondrial DNA control region sequences

The green turtle (Chelonia mydas) nesting population at Tortuguero, Costa Rica, is the largest nesting aggregation in the Atlantic, by at least an order of magnitude. Previous mitochondrial DNA (mtDNA) surveys based on limited sampling (n = 41) indicated low genetic diversity and low gene flow with other Caribbean nesting colonies. Furthermore, a survey of nuclear DNA diversity invoked the possibility of substructure within the Tortuguero rookery. To evaluate these characteristics, mtDNA control region sequences were determined for green turtles nesting at Tortuguero in 2001 (n = 157) and 2002 (n = 235). The increased sample revealed three additional haplotypes; five haplotypes are now known for Tortuguero female green turtles. Analyses of molecular variance indicated that there was no significant spatial population structure along the 30-km nesting beach. In addition, no temporal population structure was detected either between the two nesting seasons or within the nesting season. As a result of the larger sample size and additional haplotypes, estimates of genetic separation among Caribbean nesting colonies have changed and the concordance of phylogenetic and phylogeographic patterns reported in the past for green turtles in the Greater Caribbean has weakened. The five haplotypes from Tortuguero represent 36% of the haplotypes identified in green turtle nesting aggregations in the Greater Caribbean and 17% of the haplotypes known to occur in nesting or foraging aggregations in the Greater Caribbean. Haplotype diversity (0.16) and nucleotide diversity (0.0034) for the Tortuguero population are substantially lower than those for the combined rookeries in the Greater Caribbean (0.44 and 0.0078, respectively). Although comprehensive evaluation of regional genetic diversity requires nuclear DNA data, our study indicates that conserving genetic diversity in Caribbean green turtles will require careful management of the smaller rookeries in addition to the Tortuguero rookery.     

Migration of green turtles <Emphasis Type="Italic">Chelonia mydas</Emphasis> from Tortuguero,Costa Rica

During 1955–2003, flipper tags were attached to 46,983 green turtles and ten turtles were fitted with satellite transmitters at Tortuguero, Costa Rica. Eight satellite-tracked turtles stayed within 135 km of the beach and probably returned to nest after release. The internesting area is more extensive than previously documented. Post-nesting migration routes of satellite-tracked turtles varied. Seven turtles swam close to the coast and three turtles swam through oceanic waters before moving toward nearshore areas. Sea surface height anomaly maps indicate that oceanic movements were consistent with the southwestern Caribbean gyre. Circling and semi-circling turtles could have been disoriented but submergence and surface times suggest they may have been feeding in Sargassum sp. concentrations. Rapid post-nesting migrations (mean 2.2 km hr⁻¹) ended on benthic feeding grounds in shallow waters (<20 m) off Belize (n=1), Honduras (n=1) and Nicaragua (n=8). The spatial distribution of migration end points (n=10) and tag returns (n=4,669) are similar. Fishermen in Nicaragua target green turtles along migratory corridors and on foraging grounds. Management efforts are urgently needed in Nicaragua, particularly in the high-density feeding areas south and east of the Witties (N14°09 W82°45). The proximity of foraging grounds to the nesting beach (mean 512 km) may permit female turtles to invest more energy in reproduction and hence the Tortuguero population may have greater potential for recovery than other green turtle nesting populations. Recovery of the Tortuguero green turtle population will benefit countries and marine ecosystems throughout the Caribbean, especially Nicaragua.     

Breeding biology of the green turtle, Chelonia mydas (Reptilia: Cheloniidae), on Wan-An Island, PengHu archipelago. II. Nest site selection

Nest site selection of the green turtles on Wan-An Island in the summer of 1996 was determined. Turtles (Chelonia mydas) laid on average one clutch for every three emergences. Even though the total track length was 115 m on average, individual lengths varied considerably depending on the nesting beach where the turtles emerged. Limited accessibility, i.e. adequate distance from the nearest village and a well-protected environment, make beaches A and D suitable nesting beaches for green turtles on Wan-An Island. Both total track and nesting track apexes were found clustered in the interface zone, and turtles preferred to reach the vegetation zone once they emerged from the sea. It is suggested that the turtles on Wan-An Island exhibit nest site selection behavior. Based on these results and the high nest site fidelity to their first nesting beach, conservation recommendations are proposed to the county and central governments for the preservation of nesting beaches in their natural state, by prohibiting illegal sand mining and properly controlling turtle watch groups on Wan-An Island. Received: 21 November 1997 / Accepted: 24 December 1998     

Habitat use of a multispecific seagrass meadow by green turtles Chelonia mydas at Mayotte Island

We investigated the habitat use in green turtles exploiting a 13-ha multispecific seagrass meadow at Mayotte Island, south-western Indian Ocean. A phyto-ecological survey shows the occurrence of eight seagrass species, dominated by Halodule uninervis and Syringodium isoetifolium, distributed according to four distinct seagrass communities along the depth gradient. Direct underwater censuses show that green turtles occurred all over the meadow. Yet when community relative surface area was taken into account green turtles preferentially frequented the most seaward, biomass-richer S. isoetifolium-dominated community, suggesting that green turtles compensate for their intrinsically nutrient-poor herbivorous diet. Additionally, smaller (<80 cm standard curved carapace length, SCCL) individuals also preferentially occurred in the most shoreward H. univervis-dominated community where no larger (>80 cm SCCL) individuals were sighted, suggesting habitat use is indicative of diet selection and may reflect size-specific food requirements and physiology.     

Home range and habitat use of juvenile Atlantic green turtles (Chelonia mydas L.) on shallow reef habitats in Palm Beach, Florida, USA

Many animals, including sea turtles, alter their movements and home range in relation to the particular type and quality of the habitat occupied. When sufficient resources are available, individuals may develop affinities to specific areas for activities, such as foraging and (or) resting. In the case of green sea turtles (Chelonia mydas L.), after a number of years in the open ocean, juveniles recruit to shallow-water developmental habitats where they occupy distinct home ranges as they feed and grow to maturity. Our goal was to study the habitat use and home range movements of juvenile green turtles along a shallow, worm-rock reef tract in Palm Beach, Florida. Six turtles, measuring from 27.9 to 48.1 cm in straight carapace length and from 7.2 to 12.6 kg in mass, were tracked via ultrasonic telemetry from August to November 2003. Upon capture, each turtle’s esophagus was flushed via lavage to determine recently ingested foods. In addition, four turtles were recaptured and fitted with a time-depth recorder to study dive patterns. Home range areas measured with 100% minimum convex polygon and 95% fixed kernel estimators varied from 0.69 to 5.05 km² (mean=2.38±1.78 km²) and 0.73 to 4.89 km² (mean=2.09±1.80 km²), respectively. Home ranges and core areas of turtles were largely restricted to the reef tract itself, and showed considerable overlap between food and shelter sites. The mean number of dives during daylight hours (0600–1800 hours) was 84±5.0 dives, while the mean during night hours (1800–0600 hours) was 39±3.0 dives. Dives during the day were shallower (mean=3.20±1.26 m) than dives at night (mean=5.59±0.09 m). All six turtles were found to have a mixed diet of similar macroalgae and sponge fragments. Our results reveal that juvenile green turtles occupy stable home ranges along the nearshore worm-rock reefs of Southeast Florida, during the summer and fall. Determining which habitats are used by green turtles will assist conservation managers in their global effort to protect this endangered species.