Survival and remigration probabilities for loggerhead turtles (Caretta caretta) nesting in the eastern Gulf of Mexico

Few long-term mark-recapture tagging datasets exist to estimate population parameters for loggerhead sea turtle (Caretta caretta) recovery units. Using a two-state open robust design model, we analyzed a 20-year (1990–2009) mark-recapture dataset from the Keewaydin Island loggerhead nesting assemblage off the southwest coast of Florida (USA) in the eastern Gulf of Mexico. For this analysis, 2,292 turtle encounters were evaluated, representing 841 individual nesting turtles. Survival was estimated at 0.73 (95 % CI 0.69–0.76). This estimate is comparable with survival estimates elsewhere in the Peninsular Florida subpopulation and is among the lowest estimates for the Northwest Atlantic loggerhead population. We documented no changes in remigration rates or clutch frequency over time. These are the first survival and remigration probabilities estimated for a loggerhead nesting assemblage in the eastern Gulf of Mexico.     

Effects of Organized Turtle Watches on Loggerhead (Caretta caretta) Nesting Behavior and Hatchling Production in Florida

To evaluate the effects of organized turtle watches on female sea turtles and their eggs, we quantified nesting behavior and hatchling production of loggerhead turtles ( Caretta caretta ) in south Brevard Country, Florida, U.S.A. We compared the duration of five phases of nesting behavior, the directness of the turtle's return path, rate of travel during return crawl, hatching success, and hatchling emergence success between experimental and control turtles. Experimental turtles nested while observed by an organized turtle watch group consisting of at least 15 people; control turtles were not observed by a turtle watch group. Experimental turtles spent significantly less time camouflaging nest sites than did control turtles. The duration of the other four phases of nesting behavior were not significantly different between the two groups. Experimental turtles also traveled less-direct paths during return crawls, although their rates of travel were not significantly different from those of control turtles. Hatching success and hatchling emergence success were not significantly different between experimental and control turtle nests in either year. Although turtle watch groups influenced nesting behavior, they were not found to be detrimental to hatchling production. Florida's turtle watch program is a means for garnering public support for sea turtle conservation through education, and it should continue.     

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.     

Demographic composition of the feeding population of juvenile loggerhead sea turtles (Caretta caretta) off Charleston,South Carolina: evidence from mitochondrial DNA markers

To determine the origin of juvenile loggerhead turtles (Caretta caretta) that occupy the Charleston Harbor Entrance Channel at Charleston, South Carolina, USA, mitochondrial DNA restriction-fragment length polymorphisms from this feeding population were compared to haplotypes from candidate nesting populations. Previous studies have defined two major nesting populations in the southeastern USA, one corresponding to Florida and the other to Georgia/South Carolina. These nesting populations are distinguished by both unique haplotypes and frequency distributions of common haplotypes. The frequency distribution of haplotypes in the juvenile feeding-ground population was significantly different from both nesting populations, implying that the feeding aggregate is drawn from two or more nesting populations. Assuming that these turtles are derived exclusively from rookeries in the southeastern USA, a maximum likelihood estimator indicates that approximately half are from the Florida rookery and half are from the northern (Georgia/South Carolina) rookery complex. Because 91% of nesting in the southeastern USA occurs in Florida rookeries and 8% in the northern complex, the 50:50 ratio indicates that juvenile turtles from Georgia and South Carolina tend to feed preferentially near their respective rookery locations. Human encroachment on this feeding habitat may pose an especially high risk to the smaller Georgia/South Carolina rookeries.     

Hidden demographic impacts of fishing and environmental drivers of fecundity in a sea turtle population

Fisheries bycatch is a critical threat to sea turtle populations worldwide, particularly because turtles are vulnerable to multiple gear types. The Canary Current is an intensely fished region, yet there has been no demographic assessment integrating bycatch and population management information of the globally significant Cabo Verde loggerhead turtle (Caretta caretta) population. Using Boa Vista island (Eastern Cabo Verde) subpopulation data from capture–recapture and nest monitoring (2013–2019), we evaluated population viability and estimated regional bycatch rates (2016–2020) in longline, trawl, purse-seine, and artisanal fisheries. We further evaluated current nesting trends in the context of bycatch estimates, existing hatchery conservation measures, and environmental (net primary productivity) variability in turtle foraging grounds. We projected that current bycatch mortality rates would lead to the near extinction of the Boa Vista subpopulation. Bycatch reduction in longline fisheries and all fisheries combined would increase finite population growth rate by 1.76% and 1.95%, respectively. Hatchery conservation increased hatchling production and reduced extinction risk, but alone it could not achieve population growth. Short-term increases in nest counts (2013–2021), putatively driven by temporary increases in net primary productivity, may be masking ongoing long-term population declines. When fecundity was linked to net primary productivity, our hindcast models simultaneously predicted these opposing long-term and short-term trends. Consequently, our results showed conservation management must diversify from land-based management. The masking effect we found has broad-reaching implications for monitoring sea turtle populations worldwide, demonstrating the importance of directly estimating adult survival and that nest counts might inadequately reflect underlying population trends.     

Modelling the fate of marine turtle hatchlings

The SLIM oceanographic model was used to examine the fate of hatchling flatback turtles (Natator depressus) in the first two weeks of their dispersal starting at Wild Duck Island, a major turtle-nesting site in the central Great Barrier Reef region of Australia. We ran simulations to investigate the effects of spring versus neap tides, hatchling's swimming behaviour during their first three days at sea, and the location of nesting beaches. The model predicted that up to 50% of the turtle hatchlings entering the sea from the windward, southern beach remained after 14 days in shallow, nearshore waters, irrespective of tides and swimming. These waters are turbid and may be inhospitable to hatchlings. In contrast >80% of hatchlings dispersing from the leeward, northern beach were dispersed to deeper water (10-40 m) in a quasi-stationary dispersion core centred around 10 km north of the nesting beach after 14 days and the offshore spread of the turtle plume was enhanced by the hatchling's seaward swimming during the first three days. This was due to the presence of a coastal boundary layer and a stagnation zone around the northern side of island, but not the southern side. The model confirmed that dispersal from eastern Queensland flatback turtle rookeries is restricted to the lagoons and coastal waters, and that water circulation and hatchling's swimming control dispersion. The model explains why more turtles nest on the northern than the southern side. This study highlights the usefulness of oceanographic models to increase knowledge about a cryptic life stage of marine turtles.     

Counterintuitive density-dependent growth in a long-lived vertebrate after removal of nest predators

Examining the phenotypic and genetic underpinnings of life-history variation in long-lived organisms is central to the study of life-history evolution. Juvenile growth and survival are often density dependent in reptiles, and theory predicts the evolution of slow growth in response to low resources (resource-limiting hypothesis), such as under densely populated conditions. However, rapid growth is predicted when exceeding some critical body size reduces the risk of mortality (mortality hypothesis). Here we present results of paired, large-scale, five-year field experiments to identify causes of variation in individual growth and survival rates of an Australian turtle (Emydura macquarii) prior to maturity. To distinguish between these competing hypotheses, we reduced nest predators in two populations and retained a control population to create variation in juvenile density by altering recruitment levels. We also conducted a complementary split-clutch field-transplant experiment to explore the impact of incubation temperature (25 degrees or 30 degrees C), nest predator level (low or high), and clutch size on juvenile growth and survival. Juveniles in high-recruitment (predator removal) populations were not resource limited, growing more rapidly than young turtles in the control populations. Our experiments also revealed a remarkably long-term impact of the thermal conditions experienced during embryonic development on growth of turtles prior to maturity. Moreover, this thermal effect was manifested in turtles approaching maturity, rather than in turtles closer to hatching, and was dependent on population density in the post-hatching rearing environment. This apparent phenotypic plasticity in growth complements our observation of a strong, positive genetic correlation between individual body size in the experimental and control populations over the first five years of life (rG - +0.77). Thus, these Australian pleurodiran turtles have the impressive capacity to acclimate plastically to major demographic perturbations and enjoy the longer-term potential to evolve adaptively to maintain viability.     

Sex ratio of juvenile loggerhead turtles in the Mediterranean Sea: is it really 1:1?

Sex ratios are a crucial parameter for evaluating population viability. In species with complex life history patterns and temperature sex determination mechanisms, such as the loggerhead turtle (Caretta caretta), sex ratios may vary within a population and among populations. In the Mediterranean, juvenile sex ratios appear to not differ significantly from 1:1, although estimates for hatchling sex ratios are highly female biased. The immigration of males from the Atlantic has been suggested as a possible cause of such variation. Here, we present results of a multi-year investigation (2000–2011) on the sex ratios of loggerhead turtles foraging along the south Tyrrhenian coast, Western Mediterranean, with the aim of providing a better understanding of the potentially underlying forces that drive regional and age-dependent differences in sex ratios. Sex was determined through visual examination of the gonads in 271 dead turtles (curved carapace length range 29.5–89 cm). A fragment of the mitochondrial DNA control region was sequenced from 61 specimens to characterise the demographic composition of this foraging assemblage by applying a many-to-many mixed stock analysis approach. No significant association was found between sex ratios and years or size classes, although the largest size was male biased. Juvenile sex ratio was 1.56:1, which was different from an even sex ratio but still less female biased than hatchling sex ratios from Mediterranean beaches. Results of the mixed stock analysis indicate that juvenile sex ratios in the Mediterranean are largely unaffected by immigration of Atlantic individuals into the basin, as previously suggested. Continued long-term monitoring of juvenile sex ratios is necessary to detect biologically significant sex ratio shifts in the Mediterranean loggerhead turtle population.     

Estimating freshwater turtle mortality rates and population declines following hook ingestion

Freshwater turtle populations are susceptible to declines following small increases in the mortality of adults, making it essential to identify and understand potential threats. Freshwater turtles ingest fish hooks associated with recreational angling, and this is likely a problem because hook ingestion is a source of additive mortality for sea turtles. We used a Bayesian‐modeling framework, observed rates of hook ingestion by freshwater turtles, and mortality of sea turtles from hook ingestion to examine the probability that a freshwater turtle in a given population ingests a hook and subsequently dies from it. We used the results of these analyses and previously published life‐history data to simulate the effects of hook ingestion on population growth for 3 species of freshwater turtle. In our simulation, the probability that an individual turtle ingests a hook and dies as a result was 1.2–11%. Our simulation results suggest that this rate of mortality from hook ingestion is sufficient to cause population declines. We believe we have identified fish‐hook ingestion as a serious yet generally overlooked threat to the viability of freshwater turtle populations.     

Spatio-temporal patterns of juvenile marine turtle occurrence in waters of the European continental shelf

We present data spanning approximately 100 years regarding the spatial and temporal occurrence of marine turtle sightings and strandings in the northeast Atlantic from two public recording schemes and demonstrate potential signals of changing population status. Records of loggerhead (n = 317) and Kemp’s ridley (n = 44) turtles occurring on the European continental shelf were most prevalent during the autumn and winter, when waters were coolest. In contrast, endothermic leatherback turtles (n = 1,668) were most common during the summer. Analysis of the spatial distribution of hard-shell marine turtle sightings and strandings highlights a pattern of decreasing records with increasing latitude. The spatial distribution of sighting and stranding records indicates that arrival in waters of the European continental shelf is most likely driven by North Atlantic current systems. Future patterns of spatial-temporal distribution, gathered from the periphery of juvenile marine turtles habitat range, may allow for a broader assessment of the future impacts of global climate change on species range and population size.     

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     

Thalassia testudinum productivity and grazing by green turtles in a highly disturbed seagrass bed

There has been an historical decline in the seagrass beds in Maho and Francis Bays, St. John, U.S. Virgin Islands: presently (1986) there are only five small seagrass beds in shallows water. These seagrass beds are highly disturbed by heavy boat usage and are intensively grazed by the green turtle Chelonia mydas L. Fifteen to 50 boats anchor each night in the bays: anchor scars cause a loss of up to 6.5 m² d^-1 or 1.8% yr^-1 of the seagrass beds. Seagrasses regrew into such scars only minimally within a period of 7 mo. The size of the green turtle population was estimated at 50 subadults and their feeding behavior was determined by direct observation and radiotelemetry. The behavior of the green turtles differed from other observations published on the species. Here, the turtles grazed all available Thalassia testudinum, their preferred seagrass food, rather than creating discrete grazing scars, and spent all their waking hours (9 h per day) feeding. Areal productivity of T. testudinum leaves (33 to 97 mg dry wt m^-2d^-1) in the bays was at least an order of magnitude lower than published values or than the productivity of another, lessdisturbed seagrass bed on St. John, despite having comparable leaf-shoot density. Leaf shoots were stunted, fragile, achlorotic, and had only two leaves as opposed to the five leaves per shoot more typically seen. The green turtle population was near the estimated carrying capacity of T. testudinum, based on the standing crop and productivity of T. testudinum and the grazing rate of the turtles. The effect of disturbance of T. testudinum from boats and turtles was assessed by excluding these with emergent fences. Within 3 mo of protection, the areal and shoot-specific productivity of T. testudinum leaves as well as leaf size increased significantly compared to unprotected areas. Conservation efforts are recommended in Maho Bays and Francis because seagrass productivity is low, disturbance rates are higher than recovery rates, the turtles cannot increase further their feeding rate in order to compensate for such factors, and there are few alternate sources of T. testudinum on the north shore of St. John.Contribution No. 175 from West Indies Laboratory, Teague Bay, Christiansted, St. Croix, U.S. Virgin Islands 00820, USA     

Satellite tracking of migrating loggerhead sea turtles (<Emphasis Type="Italic">Caretta caretta</Emphasis>) displaced in the open sea

Loggerhead turtles (Caretta caretta) are known to migrate towards fixed, individually-specific residential feeding grounds. To study their spatial behaviour and their navigational ability, five loggerheads nesting in South Africa were captured when about to start their postnesting migration and tracked by satellite after having been displaced from their usual migratory route. The first turtle, released south of Madagascar about 1,148 km from the capture site, moved west up to mainland Africa and then reached her feeding grounds by following the coast. A second turtle, released farther away (2,140 km) close to La Réunion Island, stopped for some time on the Madagascar east coast, then turned southwards to round the island and regain the African mainland in the northwest, without however allowing us to establish the location of her residential grounds. Three other turtles were released off the Tanzanian coast, 2,193 km north of their nesting area, at the northern edge of the distribution of the feeding grounds along the African coast. All of them headed north, and one turtle found her residential grounds located north of the release site. The other two females started long-distance oceanic wanderings in which they crossed nearly the entire Indian Ocean, apparently being transported by the sea currents of the region. We conclude that adult loggerhead turtles are apparently unable to compensate for the displacement and can return to a pelagic life style characteristic of juvenile turtles. These findings suggest that South African loggerheads rely on simple orientation mechanisms, such as the use of the coastline, as a guide, and compass orientation, possibly integrated by spatiotemporal programmes and/or acquired maps of familiar sites.Communicated by R. Cattaneo-Vietti, Genova     

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.     

Trans-Pacific dispersal of loggerhead turtle hatchlings inferred from numerical simulation modeling

We used Lagrangian numerical simulations to examine the trans-Pacific dispersal processes of loggerhead turtle hatchlings. Ten thousand simulated particles were released from each of the three nesting regions in Japan and tracked for 5 years. Results showed many particles moving eastward, drifting in the Kuroshio Current followed by the Kuroshio Extension Current. However, no particles reached Baja California, a known feeding area, through passive processes, indicating that trans-Pacific transportation requires active swimming by turtles. The duration of the trans-Pacific dispersal was estimated to be at least 1.6–3.4 years, with some turtles drifting in the Kuroshio Countercurrent and remaining in the western Pacific even after 5 years. This indicates that as revealed by previous genetic studies, not all loggerheads always disperse along a trans-Pacific route. The findings showed that survival and expected growth rates varied widely according to ambient temperatures during drifting, which in turn depended on nesting location.     

Compositional stability and diversity of vascular plant communities following logging disturbance in Appalachian forests

Human-caused changes in disturbance regimes and introductions of nonnative species have the potential to result in widespread, directional changes in forest community structure. The degree that plant community composition persists or changes following disturbances depends on the balance between local extirpation and colonization by new species, including nonnatives. In this study, we examined species losses and gains, and entry of native vs. exotic species to determine how oak forests in the Appalachian Mountains might shift in species composition following a gradient of pulse disturbances (timber harvesting). We asked (1) how compositional stability of the plant community (resistance and resilience) was influenced by disturbance intensity, (2) whether community responses were driven by extirpation or colonization of species, and (3) how disturbance intensity influenced total and functional group diversity, including the nonnative proportion of the flora through time. We collected data at three spatial scales and three times, including just before, one year post-disturbance, and 10 years post-disturbance. Resistance was estimated using community distance measures between pre- and one year post-disturbance, and resilience using community distance between pre- and 10-year post-disturbance conditions. The number of colonizing and extirpated species between sampling times was analyzed for all species combined and for six functional groups. Resistance and resilience decreased with increasing timber-harvesting disturbance; compositional stability was lower in the most disturbed plots, which was driven by colonization, but not extirpation, of species. Colonization of species also led to increases in diversity after disturbance that was typically maintained after 10 years following disturbance. Most of the community-level responses were driven by post-disturbance colonization of native forbs and graminoids. The nonnative proportion of plant species tended to increase following disturbance, especially at large spatial scales in the most disturbed treatments, but tended to decrease through time following disturbance due to canopy development. The results of this study are consistent with the theory that resources released by disturbance have strong influences on species colonization and community composition. The effects of management activities tested in this study, which span a gradient of timber-harvesting disturbance, shift species composition largely via an increase in species colonization and diversity.     

Modelling the effect of fibropapilloma disease on the somatic growth dynamics of Hawaiian green sea turtles

The effect of the tumour-forming disease, fibropapillomatosis, on the somatic growth dynamics of green turtles resident in the Pala’au foraging grounds (Moloka’i, Hawai’i) was evaluated using a Bayesian generalised additive mixed modelling approach. This regression model enabled us to account for fixed effects (fibropapilloma tumour severity), nonlinear covariate functional form (carapace size, sampling year) as well as random effects due to individual heterogeneity and correlation between repeated growth measurements on some turtles. Somatic growth rates were found to be nonlinear functions of carapace size and sampling year but were not a function of low-to-moderate tumour severity. On the other hand, growth rates were significantly lower for turtles with advanced fibropapillomatosis, which suggests a limited or threshold-specific disease effect. However, tumour severity was an increasing function of carapace size—larger turtles tended to have higher tumour severity scores, presumably due to longer exposure of larger (older) turtles to the factors that cause the disease. Hence turtles with advanced fibropapillomatosis tended to be the larger turtles, which confounds size and tumour severity in this study. But somatic growth rates for the Pala’au population have also declined since the mid-1980s (sampling year effect) while disease prevalence and severity increased from the mid-1980s before levelling off by the mid-1990s. It is unlikely that this decline was related to the increasing tumour severity because growth rates have also declined over the last 10–20 years for other green turtle populations resident in Hawaiian waters that have low or no disease prevalence. The declining somatic growth rate trends evident in the Hawaiian stock are more likely a density-dependent effect caused by a dramatic increase in abundance by this once-seriously-depleted stock since the mid-1980s. So despite increasing fibropapillomatosis risk over the last 20 years, only a limited effect on somatic growth dynamics was apparent and the Hawaiian green turtle stock continues to increase in abundance.     

Environmental pollution and biodiversity: Light pollution and sea turtles in the Caribbean

We examine the impact of pollution on biodiversity by studying the effect of coastal light pollution on the sea turtle population in the Caribbean. To this end we assemble a panel data set of sea turtle nesting activity and satellite-derived measures of nighttime light. Controlling for the surveyor effort, the local economic infrastructure, and spatial spillovers, we find that nighttime light significantly reduces the number of sea turtle nests. According to data on replacement costs for sea turtles raised in captivity, our result suggests that the increase in lighting over the last two decades has resulted in the loss of close to 1800 sea turtles in the Caribbean, worth up to $288 million. Incorporating our empirical estimates into a stage-structured population model, we discover that the dynamic effect of nighttime light on future generations of sea turtles is likely to be much larger, with a cost of approximately $2.8 billion for Guadeloupe alone. More generally, our study provides a new approach to valuing the cost of environmental pollution associated with species extinction.     

Putting Longline Bycatch of Sea Turtles into Perspective

Abstract:  Although some sea turtle populations are showing encouraging signs of recovery, others continue to decline. Reversing population declines requires an understanding of the primary factor(s) that underlie this persistent demographic trend. The list of putative factors includes direct turtle and egg harvest, egg predation, loss or degradation of nesting beach habitat, fisheries bycatch, pollution, and large-scale changes in oceanographic conditions and nutrient availability. Recently, fisheries bycatch, in particular bycatch from longline fisheries, has received increased attention and has been proposed as a primary source of turtle mortality. We reviewed the existing data on the relative impact of longline bycatch on sea turtle populations. Although bycatch rates from individual longline vessels are extremely low, the amount of gear deployed by longline vessels suggests that cumulative bycatch of turtles from older age classes is substantial. Current estimates suggest that even if pelagic longlines are not the largest single source of fisheries-related mortality, longline bycatch is high enough to warrant management actions in all fleets that encounter sea turtles. Nevertheless, preliminary data also suggest that bycatch from gillnets and trawl fisheries is equally high or higher than longline bycatch with far higher mortality rates. Until gillnet and trawl fisheries are subject to the same level of scrutiny given to pelagic longlines, our understanding of the overall impact of fisheries bycatch on vulnerable sea turtle populations will be incomplete.     

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.