Search

In highly mobile philopatric species, defining the scale of natal homing is fundamental to characterizing population dynamics and effectively managing distinct populations. Genetic tools have provided evidence of regional natal philopatry in marine turtles, but extensive sharing of maternally inherited mitochondrial control region (CR) haplotypes within regions (Chelonia mydasnesting sites detected at least 2 populations, but the ubiquity of haplotype CM-A3.1 among southern rookeries decreased the power to detect differentiation. We reassessed population structure by sequencing the mitochondrial microsatellite (short tandem repeat, mtSTR) in 786 samples from 11 nesting sites spanning 700 km from Canaveral National Seashore through Dry Tortugas National Park. The mtSTR marker subdivided CM-A3.1 into 12 haplotypes that were structured among rookeries, demonstrating independent female recruitment into the Dry Tortugas and Marquesas Keys nesting populations. Combined haplotypes provided support for recognition of at least 4 management units in Florida: (1) central eastern Florida, (2) southeastern Florida, (3) Key West National Wildlife Refuge, and (4) Dry Tortugas National Park. Recapture data indicated female nesting dispersal between islands

We measured sea turtle hatchling production on 16 sea turtle nesting beaches (219.6 km) in Florida (USA) from 2002 to 2012. A standard protocol was used to sample 19 701 loggerhead Caretta caretta, 3809 green turtle Chelonia mydas, and 664 leatherback Dermochelys coriacea nest contents, representing all Florida nesting beaches. We assessed (1) annual variation in hatching (hatched eggs/total eggs) and emergence (emerged hatchlings/total eggs) successes, (2) annual hatchling production, and (3) sources of egg and hatchling mortality. Emergence success rates were extrapolated to all Florida sea turtle nesting beaches using means weighted by each beach’s nesting contribution. Weighted mean emergence success was 51.6% for loggerheads, 50.0% for green turtles, and 38.7% for leatherbacks. These estimates represent survivorship to the time hatchlings emerge from the nest. The estimated annual mean number of hatchlings produced on Florida beaches during the study period was 3 528 180 loggerheads (SD = 1 155 701), 568 098 green turtles (SD = 327 156), and 33 014 leatherbacks (SD = 17 574). Beach erosion from storms and nest predation by mammals were the principal identified sources of egg and hatchling mortality. Average emergence success ranged from 38.8 to 65.0% between years and 41.8 to 61.7% between study beaches, suggesting that a single sample year or location would not adequately represent a sea turtle population in demographic analyses of multiple year classes. We provide recommendations for analyzing hatching success and present a method of analysis that allows the inclusion of partially depredated nests. These nests are typically excluded because the original clutch size and the number of eggs removed by predators may not be known.

Anthropogenic climate change adds to the existing suite of threats to species, such as habitat degradation, by increasing extinction risk and compromising the ability of species to respond adaptively to these stressors. Because threats from anthropogenic climate change often interact synergistically with other threats, integrated assessments of the factors and processes that affect species persistence and distribution are required. We assessed the influence of coastal land use and climate change (specifically sea level rise) on the spatial distribution of nests within the largest loggerhead Caretta caretta marine turtle rookery in the Atlantic Ocean, at Melbourne Beach, Florida, from 1986 to 2006. We generated a multiple regression model based on climate change, sea-level rise and land use that describes 47% of the spatial variation in loggerhead nest- ing. Nests have shifted northward (likely in response to warming temperatures), away from inten- sive coastal development, and, surprisingly, toward areas of increased erosion. Using the Bruun Rule (an approximation of the response of the shoreline profile to sea level rise), we modeled the impacts of sea level rise of 0.25 and 0.5 m in conjunction with extrapolations of coastal develop- ment and a continued northward shift in nest distribution. We project up to a 43% decrease in beach area from 1986 to a future with 0.5 m of sea level rise and predict that loggerhead nesting will shift northward and become increasingly crowded on narrowing beaches. An implication of this study is that areas currently protected for large rookeries may not overlap with their future distributions.

The southeastern USA hosts the largest nesting concentration of loggerhead turtles Caretta caretta in the Atlantic. Regionally significant nesting also occurs along the Caribbean coast of Mexico, in Cuba, and in the Bahamas. Previous studies of North Atlantic loggerhead turtle rookeries based on a 380 bp fragment of the mitochondrial control region supported recognition of 8 demographically independent nesting populations (management units) in the Northwest Atlantic in addition to Cape Verde in the eastern Atlantic. Recent analysis of expanded mitochon- drial control region sequences revealed additional genetic diversity and increased population structure between western and eastern Atlantic loggerhead turtle rookeries. We se quenced an 817 bp mitochondrial DNA fragment in 2427 samples from nesting beaches in the southeastern USA, Cay Sal Bank, Bahamas, and Quintana Roo, Mexico. Pairwise FST comparisons, pairwise exact tests of population differentiation, and analysis of molecular variance support previously proposed management unit designations and additionally indicate that southeastern and south- western Florida rookeries should be recognized as distinct management units. Therefore, North- west Atlantic loggerhead turtle rookeries can be subdivided into 10 management units, corre- sponding to the beaches from (1) Virginia through northeastern Florida, (2) central eastern Florida, (3) southeastern Florida, (4) Dry Tortugas, Florida, (5) Cay Sal, Bahamas, (6) southwestern Cuba, (7) Quintana Roo, Mexico, (8) southwestern Florida, (9) central western Florida, and (10) northwestern Florida. We confirmed increased resolution of stock structure between many North- west Atlantic management units and the Cape Verde rookery with the expanded control region haplotypes.

As ectotherms, sea turtles are particularly sensitive to ambient temperature. Because of their charismatic megafauna and imperiled status, there is considerable interest as to how species in this taxon have responded to recent ocean warming and may respond to predicted warming trends. The fact that they are wide-ranging and evolutionarily ancient organisms suggests that marine tur- tles withstood changing climatic conditions in the past. To test if there are thermal cues that relate to dynamic nesting behaviours of loggerheads Caretta caretta and green turtles Chelonia mydas, we examined 20 yr (1989-2008) data sets of beach monitoring surveys and satellite-derived sea surface temperature (SST) from an important nesting site in east central Florida, USA, and adjacent Atlantic waters, respectively. For both species, median nesting dates became significantly earlier with higher May SSTs. However, the standard deviation of nest distributions, used as an analog for nesting sea- son length, decreased for loggerheads and, in contrast, increased for green turtles with a higher aver- age daily SST. This differential response between the species may reflect changes in reproductive physiology (e.g. internesting interval times and clutch numbers) and could have bearing on the future population dynamics of the 2 species.

Understanding the spatial movements of threatened marine species, such as sea turtles, is essential as a means of informing appropriate conservation management. Although novel tech- niques for tracking spatial movements are becoming more widely available (such as satellite track- ing), simple techniques such as mark-release-recapture remain effective. A flipper tagging and recovery program in Cuba tagged 210 loggerhead turtles over 14 yr and recovered 7% of the tags between 2 d and 3 yr later (mean = 296 d). All but one turtle was recaptured in Cuban waters, and data showed limited movement of turtles between northern and southern coasts. A further 50 turtles were recovered that had been tagged in foreign projects, the majority of which were from the USA (but also Mexico, The Bahamas, Canary Islands and Spain). A range of life stages of loggerhead tur- tles are found in Cuban waters year-round, and given that Cuba has the second largest reef in the Caribbean, it likely provides foraging habitat for significant numbers of loggerhead turtles from at least 6 different countries.

A generalized additive mixed modeling approach was used to assess somatic growth for juvenile green turtles Chelonia mydas at 4 sites in 3 ecologically distinct foraging habitats along the east central coast of Florida, USA. The 3 habitats were a man-made nuclear submarine turning basin (Trident Submarine Basin), an estuary (Indian River Lagoon), and oceanic sabellariid worm rock reefs (Sebastian Inlet and St. Lucie Power Plant). Turtles from the Indian River Lagoon site grew significantly faster than turtles from the Trident Submarine Basin and sabellariid worm rock reef sites. There were no significant differences in growth rates between the sabellariid worm rock reef and Trident Submarine Basin sites. Non-monotonic or dome-shaped growth rate functions reflecting an immature peak in growth rates were observed for all 3 habitats. Growth rates peaked in 1998 for turtles in the Trident Submarine Basin and sabellariid worm rock reef habitats; since then growth rates have declined. This temporal decline in growth rates may reflect density-dependent effects on growth as more juveniles recruit to Florida for aging grounds, a direct result of increases in nest production at the primary rookeries (Costa Rica, Florida and Mexico). Developmental habitats are important for the survival of juvenile marine turtles. This study illustrates the degree to which juvenile growth rates vary among developmental habitats, which ultimately can affect the rate of growth and recovery potential of nesting stocks.

A recently developed enzyme-linked immunosorbent assay (ELISA) was used to assess exposure of Florida wild green turtles Chelonia mydas to LETV, the herpesvirus associated with lung-eye-trachea disease (LETD). Plasma samples from 329 wild juvenile green turtles netted in the Indian River lagoon, along the Sebastian reef, or in the Trident basin (Indian River and Brevard Counties, Florida) were tested by ELISA for the presence of antibodies to LETV. Plasma samples from 180 wild juvenile green turtles were tested from these study sites to compare the prevalence of anti-LETV antibodies. While some plasma samples from each site contained anti-LETV antibodies (confirmed by Western blot analysis), plasma samples collected from the Indian River lagoon had statistically higher optical density values measured in the ELISA. No statistical differences were observed when these same plasma samples were analyzed for changes in the level of anti-LETV antibodies over 3 years (1997, 1998, and 1999). To explore the relationship between anti-LETV antibodies and fibropapillomatosis (FP), plasma from 133 green turtles scored for fibropapilloma tumor severity were tested by ELISA. There was no correlation between tumor severity and the presence of antibodies against LETV. Additional plasma samples collected from 16 tagged green turtles captured and sampled more than once (recaptures) were also tested to monitor antibody levels to LETV relative to the FP status of individual turtles over time. Again there was no clear relationship between FP tumor status and the presence of antibodies to LETV. Finally, ELISA tests on plasma from 13 nesting female turtles (9 green and 4 loggerhead) revealed high levels of anti-LETV antibodies in 11 individuals, including 2 loggerhead turtles. These results provide strong evidence that wild Florida green turtle populations at these 3 study sites are exposed to LETV or a closely related virus and that loggerhead turtles may be exposed as well. Based on a cutoff optical density value of 0.310, 71 out of the 329 wild Florida green turtles tested were seropositive for LETV antibodies (seroprevalence = 21.6%). In addition, no relationship between FP tumor severity or status and the presence of anti-LETV antibodies was found, further supporting the hypothesis that LETV and the FP-associated herpesvirus (FPHV) are separate infections of marine turtles.