Ecology of neonate loggerhead turtles inhabiting lines of downwelling near a Gulf Stream front

Neonate sea turtles disperse from nesting beaches into the open ocean and develop during a multi-year growth period at sea, but data that characterize their behavior, feeding, and habitat during this developmental period have been few. Limited information has suggested that neonate sea turtles associate with lines of floating debris and biota at areas of surface downwelling. Data from the present study come from measurements of habitat, turtle behavior, and apparent foraging preferences in areas where neonate (post-hatchling) loggerhead turtles (Caretta caretta) were observed and captured. Turtles were observed (n=293) and captured (n=241 of the 293 observed) in downwelling lines that had formed in the slope water near the Gulf Stream front off east-central Florida, USA. Catch-per-unit-effort averaged 12.4 turtles/h from a vessel moving at 2.5 knots. Turtles were largely inactive and were closely associated with floating material, especially pelagic species of Sargassum. Turtles captured along with samples of floating material and given a gastric-esophageal lavage showed a preference for animal material (35.5% of volume in habitat, 70.9% in lavage) over plant material (60.3% of volume in habitat, 22.5% in lavage). Ingested anthropogenic debris included tar (20% of turtles) and plastics (15% of turtles). Ingested animals were principally small (most <1 mm) and were typically slow-moving or non-motile species or stages. Ingested plants were most commonly Sargassum fragments or seagrasses that bore epiphytic animals. Preferred or commonly ingested animals were hydroids, copepods, and pleuston such as Janthina, Creseis, Porpita, and Halobates. Data support a hypothesis describing post-hatchling loggerheads as facultatively active but principally low-energy float-and-wait foragers both within and outside of downwelling lines. Pelagic dispersal of turtles may be best predicted by a "smart" drifter analogy wherein turtle buoyancy, surface advection, and minimal oriented movement determine their distribution at sea. Conservation implications of plastic and tar ingestion are discussed.     

Dune vegetation fertilization by nesting sea turtles

Sea turtle nesting presents a potential pathway to subsidize nutrient-poor dune ecosystems, which provide the nesting habitat for sea turtles. To assess whether this positive feedback between dune plants and turtle nests exists, we measured N concentration and delta15N values in dune soils, leaves from a common dune plant (sea oats [Uniola paniculata]), and addled eggs of loggerhead (Caretta caretta) and green turtles (Chelonia mydas) across a nesting gradient (200-1050 nests/km) along a 40.5-km stretch of beach in east central Florida, USA. The delta15N levels were higher in loggerhead than green turtle eggs, denoting the higher trophic level of loggerhead turtles. Soil N concentration and delta15N values were both positively correlated to turtle nest density. Sea oat leaf tissue delta15N was also positively correlated to nest density, indicating an increased use of augmented marine-based nutrient sources. Foliar N concentration was correlated with delta15N, suggesting that increased nutrient availability from this biogenic vector may enhance the vigor of dune vegetation, promoting dune stabilization and preserving sea turtle nesting habitat.     

Habitat use by immature loggerhead sea turtles in the Algerian Basin (western Mediterranean): swimming behaviour,seasonality and dispersal pattern

To study habitat use by loggerhead sea turtles in the Algerian Basin (western Mediterranean), ten juveniles (straight carapace length range: 39.0–63.3 cm) were tracked by satellite from March 2004 to September 2005. Swimming behaviour (characterized by speed of travel, time spent at the surface, and the cosine of turning angles) varied individually, but these differences were unrelated to body size. Despite individual differences in swimming behaviour, the ten immature loggerhead sea turtles spent most of their time in the oceanic waters of the Algerian Basin, although simulations indicated that the average tracking time (235.7 ± 98.7 SD days) was sufficiently long for them to leave the Algerian Basin and disperse through most of the Mediterranean. Furthermore, none of the ten turtles swam in any preferred direction, and their bearings were all randomly distributed. Finally, all them consistently avoided the continental shelf and did not migrate seasonally, as the average latitude, the average longitude, and the average distance of the population to the release point did not change seasonally. Seasonality also had only a weak influence in swimming behaviour, as the time spent at the surface during light hours was the only parameter that changed seasonally. We conclude that immature loggerhead sea turtles in the south of the western Mediterranean exhibit a strong fidelity to the Algerian Basin, where distribution is ruled mainly by the bathymetry, without any influence of seasonality. That fidelity to the Algerian Basin matches predictions based on genetic structuring and might result from a combination of factors: surface circulation patterns and habitat selection by the loggerhead sea turtles.     

Habitat use by loggerhead sea turtles <Emphasis Type="Italic">Caretta caretta</Emphasis> off the coast of eastern Spain results in a high vulnerability to neritic fishing gear

Previous studies of loggerhead sea turtles have concluded that drifting longlines were the main threat for immature specimens in the western Mediterranean, because immature loggerhead sea turtles mainly inhabit oceanic waters. However, recent aerial surveys have revealed large numbers of immature loggerhead sea turtles over the continental shelf of eastern mainland Spain, where turtles are exposed to neritic fishing gears but not to drifting longlines. We satellite-tracked seven loggerhead sea turtles (minimum straight carapace length (SCLmin) range: 36.5–55.0 cm) to assess whether the turtles in this region are vagrants from the adjoining oceanic regions or whether these loggerheads mostly inhabit the continental shelf. Satellite-tracking revealed that six of the tagged turtles avoided the oceanic realm and made extended use of the continental shelf, whereas only one individual could be considered a true vagrant as it avoided the continental shelf and primarily used the oceanic habitat. These results are in sharp contrast with those previously reported for immature loggerhead sea turtles of similar size from the south-western Mediterranean and fit well a relaxed ontogenic model that was recently proposed for loggerhead sea turtles in the central Mediterranean. Furthermore, these results demonstrate the vulnerability of loggerhead sea turtles of eastern mainland Spain to neritic fishing gears, as three of the seven turtles died and one was bycaught incidentally while being tracked over the continental shelf.     

Habitat use and foraging behavior of tiger sharks (<Emphasis Type="Italic">Galeocerdo cuvier</Emphasis>) in a seagrass ecosystem

Understanding the foraging behavior and spatial distribution of top predators is crucial to gaining a complete understanding of communities. However, studies of top predators are often logistically difficult and it is important to develop appropriate methods for identifying factors influencing their spatial distribution. Sharks are top predators in many marine communities, yet no studies have quantified the habitat use of large predatory sharks or determined the factors that might influence shark spatial distributions. We used acoustic telemetry and animal-borne video cameras ("Crittercam") to test the hypothesis that tiger shark (Galeocerdo cuvier) habitat use is determined by the availability of their prey. We also used Crittercam to conduct the first investigation of foraging behavior of tiger sharks. To test for habitat preferences of sharks, the observed proportion of time in each habitat for each individual was compared to the predicted values for that individual based on correlated random walk and track randomization methods. Although there was individual variation in habitat use, tiger sharks preferred shallow seagrass habitats, where their prey is most abundant. Despite multiple encounters with potential prey, sharks rarely engaged in prolonged high-speed chases, and did not attack prey that were vigilant. We propose that the tiger sharks' foraging tactic is one of stealth, and sharks rely upon close approaches to prey in order to be successful. This study shows that using appropriate analysis techniques and a variety of field methods it is possible to elucidate the factors influencing habitat use and gain insights into the foraging behavior of elusive top predators.     

Habitat use and group size of pied cormorants (<Emphasis Type="Italic">Phalacrocorax varius</Emphasis>) in a seagrass ecosystem: possible effects of food abundance and predation risk

Both food abundance and predation risk may influence habitat use decisions. However, studies of habitat use by birds in marine environments have focused only on food abundance. I investigated the possible influences of food abundance and predation risk from tiger sharks (Galeocerdo cuvier) on habitat use by pied cormorants (Phalacrocorax varius) over two spatial scales and on cormorant group size. Cormorants were usually solitary, but group size was highest in shallow habitats during months when shark density was low. Regardless of season, cormorant density within shallow habitats was higher over seagrass than sand, and cormorants were distributed between these two microhabitats proportional to prey density. Therefore, cormorants appear to respond to prey abundance at a relatively narrow spatial scale (i.e., tens of meters). At the habitat-patch scale (~1 km), the density of cormorants and their prey (teleosts) was higher in shallow habitats than in deep ones, but the density of cormorants was influenced by an interaction between water temperature (i.e., season) and habitat. There was decreased use of shallow habitats as water temperature, and the density of tiger sharks, increased. When shark density was low, cormorants were distributed across habitats roughly in proportion to the abundance of fish, suggesting that cormorants respond to food abundance at the scale of habitat patches. However, as shark abundance increased, the relative density of cormorants dropped in the dangerous shallow habitats such that there was a greater density of cormorants relative to their food in deep habitats when sharks were abundant. This suggests that pied cormorants trade-off food and risk by accepting lower energetic returns to forage in safer habitats. This study provides the first evidence that marine habitat selection by birds may be influenced by such a trade-off, and provides further evidence that tiger sharks are important in determining habitat use of their prey and mediating indirect interactions within Shark Bay.Communicated by P. W. Sammarco, Chauvin     

Tracking post-nesting movements of loggerhead turtles (Caretta caretta) with sonic and radio telemetry on the southwest coast of Florida, USA

Nine post-nesting loggerhead turtles (Caretta caretta) were tracked using sonic and radio telemetry. Tracking began immediately after the turtles left the beach and continued until contact was either lost or terminated. As sonic tags transmit continuously underwater, they were much more effective than the radio tags in determining the paths of the turtles. Radio tags transmit only at the surface and were useful in ascertaining submergence durations. For nine of the ten turtles tracked with sonic signals, the gross movement was away from the beach in a westerly direction. The tracking periods ranged from 3.35 to 8.25 h, while the straight-line movements ranged from 3.05 to 12.88 km, respectively. Sixty-seven percent of the submergence durations recorded were <3 min. This respiratory behavior suggests continuous swimming, and the paths of the turtles suggested directed movement offshore immediately after nesting. The gradual littoral slope and lack of nearshore structure in this part of the Gulf of Mexico could be contributing factors to the patterns of dispersal observed, as benthic structures provide resting and foraging habitat for loggerheads.     

Satellite tracking reveals a dichotomy in migration strategies among juvenile loggerhead turtles in the Northwest Atlantic

Few data are available on the movements and behavior of immature Atlantic loggerhead sea turtles (Caretta caretta) from their seasonal neritic foraging grounds within the western north Atlantic. These waters provide developmental habitat for loggerheads originating from several western Atlantic nesting stocks. We examined the long-term movements of 23 immature loggerheads (16 wild-caught and seven headstart turtles) characterizing their seasonal distribution, habitat use, site fidelity, and the oceanographic conditions encountered during their migrations. We identified two movement strategies: (1) a seasonal shelf-constrained north–south migratory pattern; and (2) a year-round oceanic dispersal strategy where turtles travel in the Gulf Stream to the North Atlantic and their northern dispersal is limited by the 10–15°C isotherm. When sea surface temperatures dropped below 20°C, neritic turtles began a migration south of Cape Hatteras, North Carolina (USA) where they established fidelity to the waters between North Carolina’s Outer Banks and the western edge of the Gulf Stream along outer continental shelf. Two turtles traveled as far south as Florida. Several turtles returned to their seasonal foraging grounds during subsequent summers. Northern movements were associated with both increased sea surface temperature (>21°C) and increased primary productivity. Our results indicate strong seasonal and interannual philopatry to the waters of Virginia (summer foraging habitat) and North Carolina (winter habitat). We suggest that the waters of Virginia and North Carolina provide important seasonal habitat and serve as a seasonal migratory pathway for immature loggerhead sea turtles. North Carolina’s Cape Hatteras acts as a seasonal “migratory bottleneck” for this species; special management consideration should be given to this region. Six turtles spent time farther from the continental shelf. Three entered the Gulf Stream near Cape Hatteras, traveling in the current to the northwest Atlantic. Two of these turtles remained within an oceanic habitat from 1 to 3 years and were associated with mesoscale features and frontal systems. The ability of large benthic subadults to resume an oceanic lifestyle for extended periods indicates plasticity in habitat use and migratory strategies. Therefore, traditional life history models for loggerhead sea turtles should be reevaluated.     

Different growth rates between loggerhead sea turtles (<Emphasis Type="Italic">Caretta caretta</Emphasis>) of Mediterranean and Atlantic origin in the Mediterranean Sea

We estimated for the first time the growth rates of loggerhead sea turtles of Mediterranean and of Atlantic origin found in the Mediterranean Sea, combining both skeletochronological and genetic analyses. Our growth models suggested that the growth rate of loggerhead sea turtles of Mediterranean origin was faster than that of their conspecifics with an Atlantic origin exploiting the feeding grounds in the Mediterranean Sea. The age at maturity for Mediterranean origin loggerhead sea turtles, estimated using our best fitting model, was 24 years, which suggests that loggerhead sea turtles nesting in the Mediterranean are not only smaller than those nesting in the western North Atlantic but also younger.     

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.     

Intra-Mediterranean migrations of loggerhead sea turtles (Caretta caretta) monitored by satellite telemetry

The movements of four Mediterranean loggerhead sea turtles (Caretta caretta; three females, one male) were tracked via satellite telemetry for between 108 and 457 days. Total length of the routes traveled by the turtles varied between 2554 and 7098 km, and the average travel rate was 1.2 km h^-1. Long-distance movement between the western and eastern Mediterranean basins followed a seasonal pattern and seemed to be triggered by temperature and food availability. In the autumn/winter months turtles moved from west to east in search of warmer waters, and returned to the western basin in spring, where food resources are generally more plentiful. Three (two females, one male) of the four turtles migrated eastward through the Straits of Messina, which is characterized by high fishing pressure and intense boat traffic. Information about turtle migration patterns and routes will serve to plan effective conservation strategies.     

Body temperature independence of solar radiation in free-ranging loggerhead turtles,Caretta caretta,during internesting periods

Body temperatures, ambient water temperatures, light intensities and vertical positions (depth) of eight loggerhead turtles, Caretta caretta, were monitored by small recorders during internesting periods from 1991 through 1993 off Wakayama Prefecture, Japan. Body temperatures of eight loggerhead turtles were higher than ambient water temperatures through-out their internesting periods. Light intensities were compared with body temperatures and no evidence was obtained to suggest that the raised body temperatures were caused by the direct influence of solar radiation. Body temperatures were kept higher than water temperatures in cloudy weather or even at night. Mean thermal differences between body and water temperatures were significantly different among individuals, and larger turtles had a greater mean thermal difference. Elevations in body temperatures of adult loggerhead turtles can reasonably be assumed to result from the accumulation of metabolically produced heat. Surfacing times (spent at depths shallower than 2 m) of seven turtles were only 10.3 to 38.9% of their internesting periods, with the exception of one turtle who spent 66.3% of her time at the surface. Loggerhead turtles did not seem to bask positively at the sea surface to absorb radiative heat.     

Incidental capture,direct mortality and delayed mortality of sea turtles in Australia's Northern Prawn Fishery

The species composition, catch and mortality rates of sea turtles captured incidentally by the tiger prawn fishery on Australia's northern coast in 1989 and 1990 were estimated by monitoring the fishery's catch. In 1990, the delayed rate of mortality from damage was estimated and the size composition was measured. Five species of turtles were captured: the flatback (Natator depressa, 59% of the total), loggerhead (Caretta caretta, 10%), olive ridley (Lepidochelys olivacea, 12%), green turtle (Chelonia mydas, 8%) and hawksbill (Eretmochelys imbricata, 5%). The turtle catches varied with water depth: the highest catch rates (0.068±0.006 turtles per trawl) were from trawls in water between 20 and 30 m deep, relatively few turtles (10%) were captured in water deeper than 40 m (25% of trawls). Catch rates varied with time of year: the highest catch rates were 0.098 (±0.013) turtles per trawl in winter. There was no significant difference in the overall catch rate (²= 0.047; p=0.8111; df=1) but a significant difference in mortality rate (²= 3.99; p<0.05; df=1) between the two years. The incidence of capture in the commercial fishery was 0.051 (±0.003) turtles per trawl towed for about 180 min, with 0.007 (±0.001) turtles per trawl drowning in the nets. There were no significant differences in the catch and mortality rates between the two years for any of the turtle species except the loggerhead, which had a significantly (² = 11.029; p=0.0013; df=1) lower catch rate in 1990 (0.002±0.001 turtles per trawl) than in 1989 (0.008±0.002 turtles per trawl), and a significantly higher mortality in 1990 (33%) than in 1989 (19%). Catch rates and mortality varied between the species: the flatback had the highest catch rate (0.030±0.002 turtles per trawl) but the lowest mortality (10.9%); the loggerhead had a catch rate of 0.005±0.001 turtles per trawl, and high mortality (21.9%); the olive ridley had a catch rate of 0.006±0.001 turtles per trawl and a low mortality (12.5%); the green turtle's catch rate was 0.004±0.001 per trawl and mortality 12.0%; the hawksbill had the lowest catch rate (0.002±0.001 turtles per trawl) but highest mortality (26.4%). Based on the fishing effort (27 049 d for 1989 and 25 746 d for 1990), we estimate that 5 503 (±424) turtles were caught and returned to the sea in 1989 and 5 238 (±404) in 1990, of which 567±140 drowned in 1989 and 943±187 in 1990. In 1990, an estimated 25% of all captured turtles suffered some non-lethal damage; an estimated 21% of turltes were captured comatose and 4% were injured. We conclude that, considering other threats, trawl-induced drowning is not the major impact on turtle populations in northern Australia, but that measures to reduce drowning and delayed mortality would be desirable.     

Sea Turtles in North Carolina Waters

Until the turn of the century the inshore waters of North Carolina harbored populations of sea turtles large enough to support a commercial fishery. Based on a 4- to-5-year record of sighting reports by the public, interviews of recreational fishermen, and records kept by commercial fishermen the waters continue to provide important developmental habitats for loggerhead, green, and Kemp's ridley sea turtles. Leathertback and hawksbill sea turtles infrequently entered the inshore waters. Reports from the public and commercial fishermen indicated that sea turtles were present offshore North Carolina all year and were present in inshore waters April through December. Sea turtles were encountered most frequently in the Atlantic Ocean, but seasonal encounters in some inshore waters, such as Core and Pamlico Sounds, often were greater. In early May large numbers of leatherbacks were sighted in the ocean and moved northward along the beach. Reported sightings of leatherbacks declined markedly by late June. Based on incidental captures by commercial fishermen loggerhead turtles were the most numerous species in Pamlico and Core Sounds (80%), followed by green (15%) and Kemp's ridley sea turtles (5%). Most captured turtles were immature, and all were released alive. The abundance of immature sea turtles in North Carolina inshore waters serves to emphasize that southeast U.S. estuaries are important habitats for these threatened and endangered species. This recognition supported the decision of the U.S. National Marine Fisheries Service to extend the requirement for turtle excluder devices in shrimp trawls to inshore areas during the entire year, full implementation of these requirements was achieved by December 1994.     

Hitchhikers reveal cryptic host behavior: new insights from the association between Planes major and sea turtles in the Pacific Ocean

Studies that incorporate information from habitat-specific ecological interactions (e.g., epibiotic associations) can reveal valuable insights into the cryptic habitat-use patterns and behavior of marine vertebrates. Sea turtles, like other large, highly mobile marine vertebrates, are inherently difficult to study, and such information can inform the implementation of conservation measures. The presence of epipelagic epibionts, such as the flotsam crab Planes major, on sea turtles strongly suggests that neritic turtles have recently occupied epipelagic habitats (upper 200 m in areas with >200 m depth) and that epipelagic turtles spend time at or near the surface. We quantified the effects of turtle species, turtle size, and habitat (neritic or epipelagic) on the frequency of epibiosis (F ₀) by P. major on sea turtles in the Pacific Ocean. In neritic habitats, we found that loggerhead (F ₀ = 27.6 %) and olive ridley turtles (F ₀ = 26.2 %) host crabs frequently across a wide range of body sizes, and green turtles almost never host crabs (F ₀ = 0.7 %). These results suggest that loggerheads and olive ridleys display variable/flexible epipelagic-neritic transitions, while green turtles tend to transition unidirectionally at small body sizes. In epipelagic habitats, we found that loggerheads host crabs (F ₀ = 92.9 %) more frequently than olive ridleys (F ₀ = 50 %) and green turtles (F ₀ = 38.5 %). These results suggest that epipelagic loggerheads tend to spend more time at or near the surface than epipelagic olive ridleys and green turtles. Results of this study reveal new insights into habitat-use patterns and behavior of sea turtles and display how epibiont data can supplement data from more advanced technologies to gain a better understanding of the ecology of marine vertebrates during cryptic life stages.     

The effects of wing loading and gender on the escape flights of least sandpipers (<Emphasis Type="Italic">Calidris minutilla</Emphasis>) and western sandpipers (<Emphasis Type="Italic">Calidris mauri</Emphasis>)

High body mass caused by fat storage during migration is believed to increase a bird's risk of predation by decreasing its ability to escape predators. We demonstrate the negative effect of wing loading (mass/wing area) on escape speed and angle of two migrating species of shorebird. We also show significant differences in escape performance between the species and genders. To help explain these differences, we test two potential proximate causes, wing shape and leg bone length. Wing shape is correlated with differences in escape performance between the species, but we found no correlation of wing shape or leg bone length with gender. Ultimately, greater predation risk due to habitat use or larger body size, for the species and genders respectively, may have resulted in evolution of enhanced escape ability.     

Important areas at sea for adult loggerhead sea turtles in the Mediterranean Sea: satellite tracking corroborates findings from potentially biased sources

Sea turtle populations worldwide suffer from reduced survival of immatures and adults due to fishery bycatch. Unfortunately, information about the whereabouts of turtles outside the breeding habitat is scarce in most areas, hampering the development of spatially explicit conservation plans. In the Mediterranean, recoveries of adult females flipper-tagged on nesting beaches suggest that the Adriatic Sea and Gulf of Gabès are important foraging areas for adults, but such information could be heavily biased (observing and reporting bias). In order to obtain unbiased data, we satellite-tracked seven loggerhead sea turtles after they completed nesting in the largest known Mediterranean rookery (Bay of Laganas, Zakynthos, Greece). Three females settled in the north Adriatic Sea, one in the south Adriatic Sea and two in the Gulf of Gabès area at the completion of their post-nesting migrations (one individual did not occupy a distinct foraging area). The concordance of tracking results with information from recoveries of flipper-tagged turtles suggests that the north Adriatic Sea and the Gulf of Gabès represent key areas for female adult Mediterranean loggerhead sea turtles.     

Are anthropogenic factors affecting nesting habitat of sea turtles? The case of Kanzul beach,Riviera Maya-Tulum (Mexico)

Marine coast modification and human pressure affects many species, including sea turtles. In order to study nine anthropogenic impacts that might affect nesting selection of females, incubation and hatching survival of loggerhead (Caretta caretta) and green turtle (Chelonia mydas), building structures were identified along a 5.2 km beach in Kanzul (Mexico). A high number of hotels and houses (88; 818 rooms), with an average density of 16.6 buildings per kilometer were found. These buildings form a barrier which prevents reaching the beach from inland, resulting in habitat fragmentation. Main pressures were detected during nesting selection (14.19% of turtle nesting attempts interrupted), and low impact were found during incubation (0.77%) and hatching (4.7%). There were three impacts defined as high: beach furniture that blocks out the movement of hatchlings or females, direct pressure by tourists, and artificial beachfront lighting that can potentially mislead hatchlings or females. High impacted areas showed lowest values in nesting selection and hatching success. Based on our results, we suggest management strategies to need to be implemented to reduce human pressure and to avoid nesting habitat loss of loggerhead and green turtle in Kanzul, Mexico.     

Western Mediterranean immature loggerhead turtles: habitat use in spring and summer assessed through satellite tracking and aerial surveys

An aerial survey was conducted in early spring 2002 over the continental shelf of the Balearic Archipelago to study the distribution of neritic loggerhead turtles. Furthermore, five juvenile loggerhead turtles [straight carapace length (SCL) range 37.1–48.7 cm], were instrumented with transmitters and monitored during 2003 by satellite tracking to study habitat use over a broader geographical range. The distribution of the turtles over the continental shelf matched habitat availability, as defined by depth. However, those tracked by satellite spent most of the time in the oceanic waters of the Algerian basin and generally avoided continental shelf areas. In these turtles, average speed of travel and mean cosine of turning angle did not significantly differ between habitats, indicating that avoidance of shelf areas is not due to active habitat selection. On average, tracked turtles spent 35.1±19.7% of the time at the surface, although surface time was much greater in the turtle with the shortest carapace length, suggesting that this individual had limited swimming capacity. We conclude that the transition between passive drifting and active habitat selection occurs at an SCL of about 40 cm. The turtles followed tracks that matched prevailing currents, but on some occasions they also swam upstream. Hence, the distribution of late juvenile loggerhead turtles in the southern and central western Mediterranean may reflect a combination of passive drifting and active habitat selection.Communicated by O. Kinne, Oldendorf/Luhe     

Interactions among endocrinology,seasonal reproductive cycles and the nesting biology of the female green sea turtle

We collected data on plasma levels of testosterone+5a-dihydrotestosterone (T+DHT) and corticosterone (CORT) from adult female green sea turtles (Chelonia mydas) from southern Queensland during distinct stages of their reproductive cycle. Those females capable of breeding in a given year had elevated plasma steroid levels (T+DHT 0.91ǂ.08; CORT 1.05ǂ.29 ng/ml), associated with follicular development, until courtship began in October. At the beginning of the nesting season in November plasma levels of CORT were related to when the female first nested (r²=0.06; F=10.45; P=0.01). However, they were not correlated with the number of clutches a female laid in that season (F=3.65; P=0.08). We repeatedly sampled 23 turtles over the nesting season and profiled changes in steroids immediately following oviposition of each clutch. Levels of T+DHT (range 0.41-0.58 ng/ml) and CORT (range 2.13-2.81 ng/ml) were similar through the early stages of the nesting season and inter-nesting period, and declined to near basal levels (T+DHT 0.37ǂ.03 and CORT 1.85-ng/ml) following the last clutch for the season. Steroid hormone levels were also low (T+DHT 0.38ǂ.16; CORT 0.46ǂ.21 ng/ml) in four independent post-breeding (atretic) females; samples for these females were taken at a time when body condition was presumably at the lowest for the season. Subtle changes in the nesting environment, such as variation in nesting habitat or the time of night that nesting occurred, were associated with a small and slow CORT increase. We suggest CORT is increased in nesting females to assist in lipid transfer to prepare the ovarian follicles and/or the reproductive organs for ovulation.