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

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

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

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

Origins of green turtle (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) feeding aggregations around Barbados,West Indies

Although green turtles (Chelonia mydas Linnaeus) do not nest in Barbados, the easternmost island in the Caribbean archipelago, juveniles are regularly seen foraging in nearshore waters. To examine the stock composition of this foraging population, mitochondrial (mt) DNA control region sequences were analysed from 60 juvenile (31–70 cm curved carapace length) green turtles and compared with data published for key nesting populations in the Atlantic, as well as other feeding grounds (FGs) in the Caribbean. Eight distinct haplotypes were recognised among the 60 individual green turtles sampled around Barbados. Three of the haplotypes found have only previously been reported from western Caribbean nesting beaches, and two only from South Atlantic beaches. The nesting beach origin of one of the Barbados FG haplotypes is as yet unidentified. Stock mixture analysis based on Bayesian methods showed that the Barbados FG population is a genetically mixed stock consisting of approximately equal contributions from nesting beaches in Ascension Island (25.0%), Aves Island/Surinam (23.0%), Costa Rica (19.0%), and Florida (18.5%), with a lesser but significant contribution from Mexico (10.3%). Linear regression analysis indicated no significant effects of rookery population size or distance of the rookery from the FG on estimated contributions from the source rookeries to the Barbados FG. Our data suggest that the similar-sized green turtles sampled on the Barbados FG are a mixed stock of more diverse origins than any previously sampled feeding aggregations in the Caribbean region. The relatively large contribution from the Ascension Island rookery to the Barbados FG indicates that hatchlings from distant rookeries outside the Caribbean basin enter the North Atlantic gyre and become a significant part of the pool from which eastern Caribbean foraging populations are derived. These data support a life cycle model that incorporates a tendency of immatures to migrate from their initial foraging grounds at settlement towards suitable foraging grounds closer to their natal rookeries as they mature.Communicated by P.W. Sammarco, Chauvin     

Twenty-Six Years of Green Turtle Nesting at Tortuguero, Costa Rica: An Encouraging Trend

The green turtle ( Chelonia mydas ) population that nests at Tortuguero, Costa Rica, is the largest in the Atlantic by at least an order of magnitude. Surveys to monitor the nesting activity on the northern 18 km of the 36-km beach were initiated in 1971 and extended to the entire beach in 1986. From the survey data, we estimated the total number of nesting emergences on the northern 18 km for each year from 1971 through 1996. Evaluation of the trend in nesting emergences indicated a relatively consistent increase from 1971 to the mid-1980s, constant or perhaps decreasing nesting during the late 1980s, and then resumption of an upward trend in the 1990s. Evaluation of trends in sea turtle nesting populations requires many years of data because of the large degree of annual variation in nesting numbers. The trends reported in this study must be evaluated with caution for several reasons. First, if the mean number of nests deposited by each female each year (clutch frequency) varies significantly among years, changes in the number of nesting emergences among years could reflect changes in the number of nesting females, clutch frequency, or both. Second, we only assessed the trend in one segment of the population (mature females), which may or may not represent the trend of the entire green turtle population and which, because of late maturity, may not reflect changes in juvenile mortality for many years. Third, survey frequency, and thus confidence in annual estimates, varied among years. The upward population trend must be assessed from the perspective of the catastrophic decline that the Caribbean green turtle populations have experienced since the arrival of Europeans. If careful management is continued in Costa Rica and adopted throughout the region, the collapse of the Caribbean green turtle populations—which seemed imminent in the 1950s—can be avoided.     

Estimating demographic parameters for a critically endangered marine species with frequent reproductive omission: hawksbill turtles nesting at Varanus Island,Western Australia

The hawksbill marine turtle (Eretmochelys imbricata) is listed on the IUCN Red List as critically endangered but little is known about its demography to support robust diagnosis of population trends. Moreover, adult female hawksbills do not nest each year due to environmentally mediated physiological constraints and this skipped breeding behaviour presents a major challenge in data collection and for estimating demographic parameters from such data sets. We estimated demographic parameters such as survival and breeding probabilities for a major Indo-Pacific nesting hawksbill population using a capture-mark-recapture (CMR) study and a multistate open robust design statistical modelling approach, which accounts for breeding omission and the staggered arrival and departure of nesters during each season. Our study used CMR histories for 413 nesting hawksbills tagged on Varanus Island (Western Australia) over a 4-month sampling period each year for 20 austral summer nesting seasons between 1987 and 2007. The estimated annual survival probability for these nesting hawksbills was constant over the 20 years at ca. 0.947 (95% CI: 0.91–0.97), which is encouragingly high for a population associated with industry. The estimated annual conditional nesting (breeding) probability for female hawksbills that had skipped the previous nesting season was time-specific ranging from 0.07 to 0.29 (mean = 0.18, CV = 41.3%), which presumably reflects the interaction between turtle physiology and in-water habitat quality. The mean conditional probability of breeding again having skipped 2 prior consecutive nesting seasons was ca. 0.83 (95% CI: 0.73–0.89), indicating a high frequency of breeding season omission. The annual nesting probability for females that had nested the previous season was 0, reflecting known obligate skipped breeding (reproductive omission) that is characteristic of hawksbill populations in response to high energy demands of vitellogenesis and breeding migration. These are the first estimates of annual survival and state-dependent breeding probabilities for any Indo-Pacific hawksbill stock that provide a basis for developing a better understanding of regional population dynamics for this critically endangered species.     

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

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

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

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

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

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

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.     

Variation in adult annual survival probability and remigration intervals of sea turtles

We analyzed a large dataset to quantify adult annual survival probability and remigration intervals for the Tortuguero, Costa Rica green turtle population. Annual survival probability was estimated at 0.85 (95% CI 0.75–0.92) using a recovery model and at 0.85 (95% CI 0.83–0.87) using an open robust design model. The two most common modes of remigration are 2 and 3 years. Annual survival probability is lower and remigration intervals are shorter than for other green turtle populations. Explanations for short remigration intervals include reproductive compensation due to historic population declines, availability of better quality food items, favorable environmental conditions, and short distance to the main foraging grounds. Variation in survival and remigration intervals have profound consequences for management and life history evolution. The short remigration intervals of Tortuguero green turtles partly offset mortality caused by turtle fishing in Nicaragua and mean that low juvenile survival represents a more urgent threat to the population than low adult survival. Low adult survival probability could result in selective pressure for earlier age at maturity.     

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.     

Genetic structure of the southeastern United States loggerhead turtle nesting aggregation: evidence of additional structure within the peninsular Florida recovery unit

The southeastern United States supports one of two large loggerhead turtle (Caretta caretta) nesting aggregations worldwide and is therefore critical to global conservation and recovery efforts for the species. Previous studies have established the presence of four demographically distinct nesting populations (management units) corresponding to beaches from (1) North Carolina through northeastern Florida, (2) peninsular Florida, (3) the Dry Tortugas, and (4) northwest Florida. Temporal and geographic genetic structure of the nesting aggregation was examined utilizing partial mitochondrial control region haplotype frequencies from 834 samples collected over the 2002 through 2008 nesting seasons from 19 beaches as well as previously published haplotype data. Most rookeries did not exhibit interannual genetic variation. However, the interannual variation detected did significantly impact the interpretation of spatial genetic structure in northeastern Florida. Based on pairwise F _ST comparisons, exact tests of population differentiation, and analysis of molecular variance, the present study upholds the distinctiveness of the four currently recognized management units and further supports recognition of discrete central eastern, southern (southeastern and southwestern), and central western Florida management units. Further subdivision may be warranted, but more intensive genetic sampling is required. In addition, tools such as telemetry and mark-recapture are needed to complement genetic data and overcome limitations of genetic markers in resolving loggerhead turtle rookery connectivity in the southeastern USA.     

Post-nesting migrations of loggerhead sea turtles in the Gulf of Mexico: dispersal in highly dynamic conditions

This study is the first report of post-nesting migrations of loggerhead sea turtles (Caretta caretta) nesting in Sarasota County (Florida, USA), their most important rookery in the Gulf of Mexico (GOM). In total, 28 females (curved carapace length CCL between 82.2 and 112.0 cm) were satellite-tracked between May 2005 and December 2007. Post-nesting migrations were completed in 3–68 days (mean ± SD = 23 ± 16 days). Five different migration patterns were observed: six turtles remained in the vicinity of their nesting site while the other individuals moved either to the south-western part of the Florida Shelf (n = 9 turtles), the Northeast GOM (n = 2 turtles), the South GOM (Yucatán Shelf and Campeche Bay, Mexico, and Cuba; n = 5 turtles) or the Bahamas (n = 6 turtles). In average, turtles moved along rather straight routes over the continental shelf but showed more indirect paths in oceanic waters. Path analyses coupled with remote sensing oceanographic data suggest that most of long-distance migrants reached their intended foraging destinations but did not compensate for the deflecting action of ocean currents. While six out of seven small individuals (CCL < 90 cm) remained on the Florida Shelf, larger individuals showed various migration strategies, staying on the Florida Shelf or moving to long-distance foraging grounds. This study highlights the primary importance the Western Florida Shelf in the management of the Florida Nesting Subpopulation, as well as the need of multi-national effort to promote the conservation of the loggerhead turtle in the Western Atlantic. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Genetic structure of green turtle (Chelonia mydas) peripheral populations nesting in the northwestern Pacific rookeries: evidence for northern refugia and postglacial colonization

Several green turtle (Chelonia mydas) nesting populations have been reported in the northwestern Pacific region, the northernmost limit of its distribution range. However, the population history in this region as a whole is not well understood. To clarify how the green turtle nesting populations have evolved in the northwestern Pacific region, the genetic composition of mitochondrial DNA control region sequences in the northwestern Pacific was compared with that of the other Pacific populations. We analyzed 302 samples from the northwestern Pacific rookeries, including 78 newly collected samples from rookeries in the Ryukyu Archipelago, Japan (from 24.27°N, 123.76°E to 28.45°N, 129.61°E). Our results revealed that the northwestern Pacific populations consisted of one highly endemic lineage (Clade IV) in the northwestern Pacific rookeries and two other lineages (Clades I and V) which were widely observed in other Pacific populations. We concluded that the highly endemic lineage indicated that a refugial population existed in this region during the Last Glacial Maximum, and the other two lineages indicated that colonization from populations at lower latitudes occurred during interglacial periods. The green turtle nesting populations in the present periphery of their distribution range had been thought to have their origin in colonization from lower latitudes, which served as refugia during glacial periods. However, the present results indicated that the northwestern Pacific peripheral populations have been maintained on the evolutionary timescale of this species and should be treated as long-term conservation resources.     

Strong site fidelity and longer internesting interval for solitary nesting olive ridley sea turtles in Brazil

Olive ridley sea turtles display two different types of nesting behavior: in arribada (synchronous mass nesting) or solitarily. Contrarily to arribadas, little has been published about solitary nesters. This study aimed to expand the knowledge on internesting interval and site fidelity of solitary nesting olive ridleys and to test a possible development of arribada nesting behavior. Data were collected in Sergipe (Brazil) over 125 km of beach from 10°30′S/36o23′W to 11°26′S/37o19′W, between nesting seasons 2004/2005 and 2006/2007. From 962 tagged females, 173 were seen renesting. The average internesting interval found was longer (22.35 ± 7.01 days) than previously described, which might relate to lower water temperatures during the internesting period. Olive ridleys at Sergipe showed high nesting site fidelity, with consecutive nesting events occurring in close proximity, non-randomly and dependently of previous events. Most of the consecutive nests were separated by 4.06–5.59 km. Development of arribada nesting behavior was not confirmed.     

Satellite telemetry reveals behavioural plasticity in a green turtle population nesting in Sri Lanka

Satellite transmitters were deployed on ten green turtles (Chelonia mydas) nesting in Rekawa Sanctuary (RS-80.851°E 6.045°N), Sri Lanka, during 2006 and 2007 to determine inter-nesting and migratory behaviours and foraging habitats. Nine turtles subsequently nested at RS and demonstrated two inter-nesting strategies linked to the location of their residence sites. Three turtles used local shallow coastal sites within 60 km of RS during some or all of their inter-nesting periods and then returned to and settled at these sites on completion of their breeding seasons. In contrast, five individuals spent inter-nesting periods proximate to RS and then migrated to and settled at distant (>350 km) shallow coastal residence sites. Another turtle also spent inter-nesting periods proximate to RS and then migrated to a distant oceanic atoll and made forays into oceanic waters for 42 days before transmissions ceased. This behavioural plasticity informs conservation management beyond protection at the nesting beach.     

The Importance of the Water Conservation Areas in the Everglades to the Endangered Wood Stork (Mycteria americana)

During 1985–1989, numbers of the endangered Wood Stork ( Mycteria americana ) in the Water Conservation Areas of the Everglades, Florida, showed an annual peak in February or March of 1233 to 7874 birds. The annual maxima are significantly greater in dry years than in wet years (P < 0.05). Most storks are nonbreeders and are found foraging in open habitats along the eastern and southern parts of Conservation Area 1 and Conservation Area 2A and along the west-central side of Conservation Area 3A. In dry years, large numbers move into the southern half of Conservation Area 3A. We estimated that in spring, the total southeastern United States population of Wood Storks is between 14,000 and 20,000 individuals. The annual maxima of the water conservation areas were at least 8% to 10% of the total southeastern U.S. population in wet years and possibly as much as 55% in dry years. The Water Conservation Areas appear to be critical foraging habitat for wintering storks, especially during drought years when most of the rest of south Florida is dry. Changes in the management of these areas could have a major impact on the status of storks throughout the southeastern United States.     

Regional and annual variation in plasma steroids and metabolic indicators in female green turtles, <Emphasis Type="Italic">Chelonia mydas</Emphasis>

Variation in environmental conditions at a foraging area or at a nesting rookery has the potential to impact reproductive output of green sea turtles (Chelonia mydas) by affecting food resources or the nesting substrate. In this paper we test whether turtles‘ physiological characteristics reflect variation in relevant environmental conditions. We did this by profiling metabolic and hormonal markers among (1) non-vitellogenic females from three different foraging areas and (2) nesting females from different rookeries and breeding seasons. Among the non-vitellogenic females, the highest plasma triglyceride concentrations (4.29 mmol/l) and the lowest plasma cholesterol concentrations (1.27 mmol/l) were found in non-vitellogenic females residing in Moreton Bay during the El Niño year of 1997. Furthermore, during 1997, these Moreton Bay females had higher plasma triglyceride and lower cholesterol concentrations than those recorded in non-vitellogenic females foraging at Heron Reef (triglyceride 1.22 mmol/l and cholesterol 4.53 mmol/l) and Shoalwater Bay (triglyceride 1.69 mmol/l and cholesterol 3.50 mmol/l) in the same year. Among nesting turtles, those nesting at Raine Island had low mean plasma triglyceride concentrations during the high density 1996 nesting season. For those nesting at Heron Island, the mean triglyceride concentrations were the lowest during the 1997 nesting season. This is the first time that hormone and metabolic markers have been used in concert to compare the physiological condition of nesting and foraging sea turtles and its relationship with the environment. Collectively, our data indicate that variation in the environmental conditions at both foraging and nesting areas are reflected at a physiological level. Moreover, our study indicates that turtles feeding during El Niño years are able to attain higher levels of body condition, and that physiological data combined with morphometric data is a useful proxy for assessing the condition of turtles in foraging areas.     

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.     

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.