Kemp's Ridley Research Articles

Ophthalmic variables in rehabilitated juvenile Kemp's ridley sea turtles (Lepidochelys kempii).

To determine central corneal thickness (total corneal thickness [TCT], epithelial thickness [ET], and stromal thickness [ST]), anterior chamber depth (ACD), and intraocular pressure (IOP) in Kemp's ridley sea turtles (Lepidochelys kempii). Prospective cross-sectional study. 25 healthy rehabilitated juvenile Kemp's ridley sea turtles. PROCEDURES; Body weight and straight-line standard carapace length (SCL) were recorded. All turtles underwent a complete anterior segment ophthalmic examination. Central TCT, ET, ST, and ACD were determined by use of a spectral-domain optical coherence tomography device. Intraocular pressure was determined with a rebound tonometer; the horse setting was used to measure IOP in all 25 turtles, and the undefined setting was also used to measure IOP in 20 turtles. For each variable, 3 measurements were obtained bilaterally. The mean was calculated for each eye and used for analysis purposes. The mean ± SD body weight and SCL were 3.85 ± 1.05 kg (8.47 ± 2.31 lb) and 29 ± 3 cm, respectively. The mean ± SD TCT, ET, ST, and ACD were 288 ± 23 μm, 100 ± 6 μm, 190 ± 19 μm, and 581 ± 128 μm, respectively. Mean ± SD IOP was 6.5 ± 1.0 mm Hg when measured with the horse setting and 3.8 ± 1.1 mm Hg when measured with the undefined setting. Results provided preliminary reference ranges for objective assessment of ophthalmic variables in healthy juvenile Kemp's ridley sea turtles.

Estimating the historic size and current status of the Kemp's ridley sea turtle (Lepidochelys kempii) population

AbstractThis study is a quantitative evaluation of historic nesting levels of the Kemp's ridley sea turtle (Lepidochelys kempii) in 1947 based on (1) the Herrera film of a 1947 arribada, (2) Hildebrand's 1947 report regarding the 1947 arribada shown in the Herrera film, (3) historic documentation regarding the Herrera film, and (4) current nesting characteristics related to arribada size relative to total nests for a season. Using this information in a quantitative approach, we estimate a total of approximately 26 916 nests during the 1947 arribada recorded by Herrera. Based on current nesting trends, we also predict that this would equate to approximately 121 517 total nests for the 1947 season (range of 82 514–209 953), which would represent approximately 48 607 nesting females (range of 33 006–83 981). This suggests that during and prior to the 1947 nesting season a relatively robust population of Kemp's ridleys existed, which could support arribadas consisting of at least 26 916 females. The results of the current study indicate that from 1947 through 1985 (the lowest point in the decline of Kemp's ridley nesting) the Kemp's ridley population underwent a 99.4% decline (range of 99.2–99.7%) from an estimated 121 517 nests per season in 1947 to 702 nests per season in 1985. Although the Kemp's ridley population has been recovering since the 1985 season, it has deviated from its exponential recovery rate and has declined in recent years. The current levels of nesting (12 053 nests in 2014) are still relatively low at 9.9% (range of 5.7–14.6%) of the total estimated nests that occurred in 1947. It is currently not clear whether this population will recover to historic levels considering recent nesting trends and due to a variety of threats that may hinder its recovery.

Assessment of ground transportation stress in juvenile Kemp's ridley sea turtles (Lepidochelys kempii).

Sea turtle rehabilitation centres frequently transport sea turtles for long distances to move animals between centres or to release them at beaches, yet there is little information on the possible effects of transportation-related stress ('transport stress') on sea turtles. To assess whether transport stress is a clinically relevant concern for endangered Kemp's ridley sea turtles (Lepidochelys kempii), we obtained pre-transport and post-transport plasma samples from 26 juvenile Kemp's ridley sea turtles that were transported for 13 h (n = 15 turtles) or 26 h (n = 11 turtles) by truck for release at beaches. To control for effects of handling, food restriction and time of day, the same turtles were also studied on 'control days' 2 weeks prior to transport, i.e. with two samples taken to mimic pre-transport and post-transport timing, but without transportation. Blood samples were analysed for nine clinical health measures (pH, pCO2, pO2, HCO3, sodium, potassium, ionized calcium, lactate and haematocrit) and four 'stress-associated' parameters (corticosterone, glucose, white blood cell count and heterophil-to-lymphocyte ratio). Vital signs (heart rate, respiratory rate and cloacal temperature) were also monitored. Corticosterone and glucose showed pronounced elevations due specifically to transportation; for corticosterone, this elevation was significant only for the longer transport duration, whereas glucose increased significantly after both transport durations. However, clinical health measures and vital signs showed minimal or no changes in response to any sampling event (with or without transport), and all turtles appeared to be in good clinical health after both transport durations. Thus, transportation elicits a mild, but detectable, adrenal stress response that is more pronounced during longer durations of transport; nonetheless, Kemp's ridley sea turtles can tolerate ground transportation of up to 26 h in good health. These results are likely to depend on specific transportation and handling protocols.

Head-Started Kemp's Ridley Turtle (Lepidochelys kempii) Nest Recorded in Florida: Possible Implications

Abstract A head-started Kemp's ridley sea turtle (Lepidochelys kempii) was documented nesting on South Walton Beach, Florida on 25 May 2015. This record supports the possibility that exposure to Florida waters after being held in captivity through 1–3 yrs of age during the head-starting process may have influenced future nest site selection of this and perhaps other Kemp's ridley turtles. Such findings could have important ramifications for marine water experimentation and release site selection for turtles that have been reared in captivity.

Migratory corridors of adult female Kemp's ridley turtles in the Gulf of Mexico

For many marine species, locations of migratory pathways are not well defined. We used satellite telemetry and switching state-space modeling (SSM) to define the migratory corridor used by Kemp's ridley turtles (Lepidochelys kempii) in the Gulf of Mexico. The turtles were tagged after nesting at Padre Island National Seashore, Texas, USA from 1997 to 2014 (PAIS; n=80); Rancho Nuevo, Tamaulipas, Mexico from 2010 to 2011 (RN; n=14); Tecolutla, Veracruz, Mexico from 2012 to 2013 (VC; n=13); and Gulf Shores, Alabama, USA during 2012 (GS; n=1). The migratory corridor lies in nearshore Gulf of Mexico waters in the USA and Mexico with mean water depth of 26m and a mean distance of 20km from the nearest mainland coast. Migration from the nesting beach is a short phenomenon that occurs from late-May through August, with a peak in June. There was spatial similarity of post-nesting migratory pathways for different turtles over a 16year period. Thus, our results indicate that these nearshore Gulf waters represent a critical migratory habitat for this species. However, there is a gap in our understanding of the migratory pathways used by this and other species to return from foraging grounds to nesting beaches. Therefore, our results highlight the need for tracking reproductive individuals from foraging grounds to nesting beaches. Continued tracking of adult females from PAIS, RN, and VC nesting beaches will allow further study of environmental and bathymetric components of migratory habitat and threats occurring within our defined corridor. Furthermore, the existence of this migratory corridor in nearshore waters of both the USA and Mexico demonstrates that international cooperation is necessary to protect essential migratory habitat for this imperiled species.

Baseline Corneal Sensitivity and Duration of Action of Proparacaine in Rehabilitated Juvenile Kemp's Ridley Sea Turtles (Lepidochelys kempii)

Abstract Corneal sensitivity and the duration of action of a topical anesthetic drop, proparacaine, were evaluated prospectively. Baseline corneal touch threshold (CTT) was determined using a Cochet-Bonnet esthesiometer in 25 healthy, rehabilitated Kemp's ridley sea turtles (Lepidochelys kempii). Corneal touch threshold was defined as the filament length required to elicit a blink in at least three out of five applications. The onset and duration of action of proparacaine was determined in nine of the Kemp's ridley sea turtles. One drop of proparacaine was applied to each eye and the CTT was subsequently measured at 1, 5, 15, 30, and 45 min. Results demonstrated that the mean CTT for the Kemp's ridley sea turtles was 5.7 cm, with a median of 6 cm. Additionally, proparacaine had an onset of action within 1 min after application (17/18 eyes). The duration of action of proparacaine exceeded the 45 min time limit in all eyes. This study shows that Kemp's ridley sea turtles have an exceptionally sensitive corn...

Deepwater Horizon oil spill impacts on sea turtles could span the Atlantic.

We investigated the extent that the 2010 Deepwater Horizon oil spill potentially affected oceanic-stage sea turtles from populations across the Atlantic. Within an ocean-circulation model, particles were backtracked from the Gulf of Mexico spill site to determine the probability of young turtles arriving in this area from major nesting beaches. The abundance of turtles in the vicinity of the oil spill was derived by forward-tracking particles from focal beaches and integrating population size, oceanic-stage duration and stage-specific survival rates. Simulations indicated that 321 401 (66 199–397 864) green (Chelonia mydas), loggerhead (Caretta caretta) and Kemp's ridley (Lepidochelys kempii) turtles were likely within the spill site. These predictions compared favourably with estimates from in-water observations recently made available to the public (though our initial predictions for Kemp's ridley were substantially lower than in-water estimates, better agreement was obtained with modifications to mimic behaviour of young Kemp's ridley turtles in the northern Gulf). Simulations predicted 75.2% (71.9–76.3%) of turtles came from Mexico, 14.8% (11–18%) from Costa Rica, 5.9% (4.8–7.9%) from countries in northern South America, 3.4% (2.4–3.5%) from the United States and 1.6% (0.6–2.0%) from West African countries. Thus, the spill's impacts may extend far beyond the current focus on the northern Gulf of Mexico.

TISSUE ENZYME ACTIVITIES IN KEMP'S RIDLEY TURTLES (LEPIDOCHELYS KEMPII).

This study determined the tissue distribution and activities of eight enzymes in 13 juvenile Kemp's ridley turtles (Lepidochelys kempii) that died after stranding. Samples from the liver, kidney, skeletal muscle, cardiac muscle, pancreas, lung, small intestine, and spleen were evaluated for activities of alanine aminotransferase (ALT), alkaline phosphatase (ALP), amylase, aspartate aminotransferase (AST), creatine kinase (CK), γ-glutamyl transferase (GGT), lactate dehydrogenase (LDH), and lipase. AST, CK, and LDH activities were highest in cardiac and skeletal muscle but were also found in all other tissues. Amylase and lipase activities were highest in the pancreas and low in all other tissues. ALP activity was highest in the lung. ALT activity was highest in liver, kidney, and cardiac muscle, and GGT activity was highest in the kidney, but activities of these enzymes were low in all tissues. These data may assist clinicians in interpretation of plasma enzyme activities of Kemp's ridley turtles.

The ontogeny of morphological defenses in Kemp's ridley (Lepidochelys kempii) and loggerhead (Caretta caretta) sea turtles.

Marine turtles are large reptiles that compensate for high juvenile mortality by producing hundreds of hatchlings during a long reproductive lifespan. Most hatchlings are taken by predators during their migration to, and while resident in, the open ocean. Their survival depends upon crypticity, minimizing movement to avoid detection, and foraging efficiently to grow to a size too difficult for predators to either handle or swallow. While these behavioral antipredator tactics are known, changes in morphology accompanying growth may also improve survival prospects. These have been only superficially described in the literature. Here, we compare the similarities and differences in presumed morphological defenses of growing loggerhead (Caretta caretta) and Kemp's ridley (Lepidochelys kempii) posthatchlings, related species that differ in growth rate, timing of habitat shift (the return from oceanic to neritic locations), and size at maturity. In both species, vertebral spination and carapace widening increase disproportionally as small turtles grow, but later in ontogeny, the spines regress, sooner in ridley than in loggerhead turtles. Carapace widening occurs in both species but loggerheads are always longer than they are wide whereas in Kemp's ridley turtles, the carapace becomes as wide as long. Our analysis indicates that these changes are unrelated to when each species shifts habitat but are related to turtle size. We hypothesize that the spines function in small turtles as an early defense against gape-limited predators, but changes in body shape function throughout ontogeny-initially to make small turtles too wide to swallow and later by presenting an almost flat and hardened surface that large predators (such as a sharks) are unable to grasp. The extremely wide carapace of the Kemp's ridley may compensate for its smaller adult size (and presumed greater vulnerability) than the loggerhead.

Direct evidence of swimming demonstrates active dispersal in the sea turtle ‘lost years’

Although oceanic dispersal in larval and juvenile marine animals is widely studied, the relative contributions of swimming behavior and ocean currents to movements and distribution are poorly understood [1-4]. The sea turtle "lost years" [5] (often referred to as the surface-pelagic [6] or oceanic [7] stage) are a classic example. Upon hatching, young turtles migrate offshore and are rarely observed until they return to coastal waters as larger juveniles [5]. Sightings of small turtles downcurrent of nesting beaches and in association with drifting organisms (e.g., Sargassum algae) led to this stage being described as a "passive migration" during which turtles' movements are dictated by ocean currents [5-10]. However, laboratory and modeling studies suggest that dispersal trajectories might also be shaped by oriented swimming [11-15]. Here, we use an experimental approach designed to directly test the passive-migration hypothesis by deploying pairs of surface drifters alongside small green (Chelonia mydas) and Kemp's ridley (Lepidochelys kempii) wild-caught turtles, tracking their movements via satellite telemetry. We conclusively demonstrate that these turtles do not behave as passive drifters. In nearly all cases, drifter trajectories were uncharacteristic of turtle trajectories. Species-specific and location-dependent oriented swimming behavior, inferred by subtracting track velocity from modeled ocean velocity, contributed substantially to individual movement and distribution. These findings highlight the importance of in situ observations for depicting the dispersal of weakly swimming animals. Such observations, paired with information on the mechanisms of orientation, will likely allow for more accurate predictions of the ecological and evolutionary processes shaped by animal movement.

Messy legacy of Gulf oil spill

There's something amiss with iconic marine animals in the Gulf of Mexico. Five years on from the largest oil spill in US history; effects are still lingering. Sea turtle populations are in retreat, dolphins are in poor shape and whales are avoiding their usual hunting grounds. The explosion of the Deepwater Horizon rig on Apr 20, 2010 killed 11 workers and the subsequent oil spill wreaked havoc on the region's wildlife. There was an immediate reverse in the recovery of the world's most endangered sea turtle. Until that point, the number of nests of the Kemp's ridley turtle, which neared extinction in the 19808, had been growing for two decades.

Factors influencing survivorship of rehabilitating green sea turtles (Chelonia mydas) with fibropapillomatosis.

Marine turtle fibropapillomatosis (FP) is a debilitating, infectious neoplastic disease that has reached epizootic proportions in several tropical and subtropical populations of green turtles (Chelonia mydas). FP represents an important health concern in sea turtle rehabilitation facilities. The objectives of this study were to describe the observed epidemiology, biology, and survival rates of turtles affected by FP (FP+ turtles) in a rehabilitation environment; to evaluate clinical parameters as predictors of survival in affected rehabilitating turtles; and to provide information about case progression scenarios and potential outcomes for FP+ sea turtle patients. A retrospective case series analysis was performed using the medical records of the Georgia Sea Turtle Center (GSTC), Jekyll Island, Georgia, USA, during 2009-2013. Information evaluated included signalment, morphometrics, presenting complaint, time to FP onset, tumor score (0-3), co-morbid conditions, diagnostic test results, therapeutic interventions, and case outcomes. Overall, FP was present in 27/362 (7.5%) of all sea turtles admitted to the GSTC for rehabilitation, either upon admittance or during their rehabilitation. Of these, 25 were green and 2 were Kemp's ridley turtles. Of 10 turtles that had only plaque-like FP lesions, 60% had natural tumor regression, all were released, and they were significantly more likely to survive than those with classic FP (P = 0.02 [0.27-0.75, 95% CI]). Turtles without ocular FP were eight times more likely to survive than those with ocular FP (odds ratio = 8.75, P = 0.032 [1.21-63.43, 95% CI]). Laser-mediated tumor removal surgery is the treatment of choice for FP+ patients at the GSTC; number of surgeries was not significantly related to case outcome.

Diagnosis and management of Enterococcus spp infections during rehabilitation of cold-stunned Kemp's ridley turtles (Lepidochelys kempii): 50 cases (2006-2012).

To evaluate clinical data for cold-stunned Kemp's ridley turtles (Lepidochelys kempii) with Enterococcus spp infections during rehabilitation. Retrospective case series. 50 stranded cold-stunned Kemp's ridley turtles hospitalized between 2006 and 2012. Medical records for turtles from which Enterococcus spp were isolated were reviewed retrospectively, and clinical data, including morphometric data, body temperature at admission, physical examination findings, antimicrobial medication history, history of medications administered IV, environmental data, day of diagnosis, clinical signs at diagnosis, microbiological testing results, sources of positive culture results, hematologic and plasma biochemical data, cytologic and histopathologic results, radiographic findings, antimicrobial treatments, time to first negative culture result, treatment duration, results of subsequent cultures, and case outcome, were collated and analyzed. Enterococcus spp were isolated from bacteriologic cultures of blood, bone, joint, and respiratory tract samples and a skin lesion, with supporting evidence of infection provided by histopathologic, cytologic, and radiographic data. Positive culture results were associated with clinical problems such as lethargy, anorexia, and lameness. Most (34/43 [79%]) turtles for which an antemortem diagnosis was made survived with treatment and were released into the wild. Cold-stunned Kemp's ridley turtles may be affected by serious Enterococcus spp infections during rehabilitation. Recognition and treatment of these infections are important for successful rehabilitation.

Brevetoxin exposure, superoxide dismutase activity and plasma protein electrophoretic profiles in wild-caught Kemp's ridley sea turtles (Lepidochelys kempii) in southwest Florida

Because of their vulnerable population status, assessing exposure levels and impacts of toxins on the health status of Gulf of Mexico marine turtle populations is critical. From 2011 to 2013, two large blooms of the red tide dinoflagellate, Karenia brevis, occurred along the west coast of Florida USA (from October 2011 to January 2012 and October 2012 to April 2013). Other than recovery of stranded individuals, it is unknown how harmful algal blooms affected the Kemp's ridley sea turtles (Lepidochelys kempii) inhabiting the affected coastal waters. It is essential to gather information regarding brevetoxin exposure in these turtles to determine if it poses a threat to marine turtle health and survival. From April 2012 to May 2013, we collected blood from 13 immature Kemp's ridley turtles captured in the Pine Island Sound region of the Charlotte Harbor estuary. Nine turtles were sampled immediately after or during the red tide events (bloom group) while four turtles were sampled between the events (non-bloom group). Plasma was analyzed for total brevetoxins (reported as ng PbTx-3eq/mL), superoxide dismutase (SOD) activity, total protein concentration and protein electrophoretic profiles (albumin, alpha-, beta- and gamma-globulins). Brevetoxin concentrations ranged from 7.0 to 33.8ng PbTx-3eq/mL. Plasma brevetoxin concentrations in the nine turtles sampled during or immediately after the red tide events were significantly higher (by 59%, P=0.04) than turtles sampled between events. No significant correlations were observed between plasma brevetoxin concentrations and plasma proteins or SOD activity, most likely due to the small sample size; however alpha-globulins tended to increase with increasing brevetoxin concentrations in the bloom group. Smaller (carapace length and mass) bloom turtles had higher plasma brevetoxin concentrations than larger bloom turtles, possibly due to a growth dilution effect with increasing size. The research presented here improves the current understanding of potential impacts of environmental brevetoxin exposure on marine turtle health and survival.

Sea Turtle Funding Dries Up

In December, as we celebrated the 40th anniversary of the Endangered Species Act and all of its accomplishments, the U.S. Fish and Wildlife Service (USFWS) terminated support for the recovery of an icon: the Kemp's ridley sea turtle ( Lepidochelys kempii ). This sea turtle nearly slipped into

Kemp’s ridley Lepidochelys kempii nesting abundance in Texas, USA: a novel approach using genetics to improve population census

Accurate estimates of the annual numbers of nesting females are critical for assessing sea turtle populations. Nesting by Kemp's ridley Lepidochelys kempii turtles has significantly increased at Padre Island National Seashore and nearby beaches in Texas, USA. Four nests were observed in Texas during 1995 and a record of 209 in 2012. However, it is unclear how many clutches are laid by the same females. We used a genetic approach to infer the number of individ- ual nesters from genotypes determined from dead embryos and hatchlings sampled from clutches. Mitochondrial DNA sequencing was combined with nuclear DNA analysis at 10 micro satellite loci to match genotypes for nesters and offspring of unknown parentage in over 50% of the unas- signed nests. Our results indicate that traditional methods, based on observed tagged turtles, have underestimated the number of Kemp's ridleys nesting in Texas. We demonstrate how genetic approaches can be incorporated into population assessments when direct census of adult animals is not feasible. This approach also provides a basis to apply capturemarkrecapture techniques to assess the impact of events, such as the recent oil spill, on the population via sampling of nests to identify and track individual nesters over time.

Predicting the distribution of oceanic-stage Kemp's ridley sea turtles.

The inaccessibility of open ocean habitat and the cryptic nature of small animals are fundamental problems when assessing the distribution of oceanic-stage sea turtles and other marine animals sharing similar life-history traits. Most methods that estimate patterns of abundance cannot be applied in situations that are extremely data limited. Here, we use a movement ecology framework to generate the first predicted distributions for the oceanic stage of the Kemp's ridley sea turtle (Lepidochelys kempii). Our simulations of particle dispersal within ocean circulation models reveal substantial annual variation in distribution and survival among simulated cohorts. Such techniques can help prioritize areas for conservation, and supply inputs for more realistic demographic models attempting to characterize population trends.

Using an ocean model to predict likely drift tracks of sea turtle carcasses in the north central Gulf of Mexico

From March through July 2011, an increased number of Kemp's ridley sea turtles Lepidochelys kempii were reported stranded on the islands, beaches and shorelines of Louisiana, Mississippi and Alabama. Members of the National Sea Turtle Stranding and Salvage Network responded, documenting the location and physical condition of each turtle. This report describes an ocean physical model-based analysis of the spring and summer 2011 Mississippi stranding events. Included within this group of strandings was 1 satellite-tagged moribund Kemp's ridley turtle, initially alive and tagged by the Institute for Marine Mammal Studies for a site fidelity study. Data from this tracking event provided an accurate time sequence of 58 h, during which the animal was presumed to be drifting, based on observed characteristics that were typical of a float- ing carcass. Turtle drift data were combined with output from the America SEAS (AMSEAS) hydrodynamic model to provide an estimate of leeway. The AMSEAS model was then applied to an additional 247 stranded turtles to produce 5 d Lagrangian backtrack drifts to derive mortality source location probability maps. Based on the model presented in this study, the majority of mor- talities appeared to have occurred in eastern Louisiana state waters.

Geographical variation in hurricane impacts among sea turtle populations

AbstractAimHurricanes bring wind and rainfall that can have dramatic effects on coastal ecosystems, which provide important nesting locations for some migratory species. We investigated the frequency with which hurricanes impact spatially and biologically distinct sea turtle nesting populations to understand whether the reproductive biology of sea turtles can buffer population‐level impacts of these disturbances.LocationNorth‐western Atlantic and north‐eastern Pacific Oceans.MethodsHistorical hurricane paths from 1970 to 2007 were combined into a spatial layer of seasonal storm frequency, which we used to quantify the frequency of impacts on sea turtle nesting sites. This was done by comparing spatio‐temporal patterns of hurricane frequency among nesting sites used by different species and spatially/biologically distinct populations (‘regional management units’).ResultsHurricanes affected 97% of sea turtle nesting beaches (n = 2444) over four decades, and the seasonal incidence of these storms overlapped substantially with sea turtle nesting and egg incubation periods. The spatial distribution of storms, in relation to the distribution of species and regional management units, determined relative exposure to large storm events. Green (Chelonia mydas), hawksbill (Eretmochelys imbricata) and leatherback (Dermochelys coriacea) turtle nesting beaches experienced relatively frequent storms; loggerhead (Caretta caretta) and Kemp's ridley (Lepidochelys kempii) turtle nesting beaches experienced relatively fewer storms; and olive ridley turtle (Lepidochelys olivacea) nesting sites were least affected.Main conclusionsExtreme weather events are common features of coastal environments and may impact sea turtles by altering nesting habitat quality (through sand erosion and accretion) and lowering within‐season reproductive success by drowning incubating embryos or eroding nests. The unique reproductive attributes of sea turtles (i.e. individual females reproduce at 2–5‐year intervals, and when reproducing lay 2–7 clutches of c. 100 large eggs at c. 2‐week intervals) may be uniquely suited to exploiting highly disturbed nesting habitats. The impacts of hurricanes on sea turtle populations may be limited because even in severe storm seasons only a proportion of adult females are reproducing, and only those eggs incubating at the time of storm impact will be directly affected. Understanding whether the frequency of large storms influences long‐term population dynamics will aid in the development of effective local and regional management plans for sea turtle recovery efforts.

Forecasting range expansion into ecological traps: climate‐mediated shifts in sea turtle nesting beaches and human development

Some species are adapting to changing environments by expanding their geographic ranges. Understanding whether range shifts will be accompanied by increased exposure to other threats is crucial to predicting when and where new populations could successfully establish. If species overlap to a greater extent with human development under climate change, this could form ecological traps which are attractive to dispersing individuals, but the use of which substantially reduces fitness. Until recently, the core nesting range for the Critically Endangered Kemp's ridley sea turtle (Lepidochelys kempii) was ca. 1000 km of sparsely populated coastline in Tamaulipas, Mexico. Over the past twenty-five years, this species has expanded its range into populated areas of coastal Florida (>1500 km outside the historical range), where nesting now occurs annually. Suitable Kemp's ridley nesting habitat has persisted for at least 140 000 years in the western Gulf of Mexico, and climate change models predict further nesting range expansion into the eastern Gulf of Mexico and northern Atlantic Ocean. Range expansion is 6-12% more likely to occur along uninhabited stretches of coastline than are current nesting beaches, suggesting that novel nesting areas will not be associated with high levels of anthropogenic disturbance. Although the high breeding-site fidelity of some migratory species could limit adaptation to climate change, rapid population recovery following effective conservation measures may enhance opportunities for range expansion. Anticipating the interactive effects of past or contemporary conservation measures, climate change, and future human activities will help focus long-term conservation strategies.