Migratory activity by hatchling loggerhead sea turtles (Caretta caretta L.): evidence for divergence between nesting groups

The South Florida subpopulation of loggerhead sea turtles (Caretta caretta L.) nests with great fidelity on either the southeast or the southwest coast of Florida, USA. The hatchlings that emerge from those nests must swim in opposite directions and search for different surface currents to migrate away from continental shelf waters. In this laboratory study, we compared the pattern of swimming activity shown by the hatchlings from each coast over the first 6 days of migration. Turtles from both coasts were equally active during their “frenzy” period (the first 24 h of swimming) and during the daylight hours of the 5 days that followed (the “postfrenzy” period). However, the west coast turtles were significantly more active than the east coast turtles during the nocturnal portion of the postfrenzy period. This difference may be related to the greater distance southwest coast turtles must negotiate to locate surface currents for transport out of the Gulf of Mexico and into the Atlantic Ocean basin. These differing behavioral strategies may be genetically determined, as similar correspondence between activity and distance is well known among migratory populations of birds and fish and is often based upon inherited programs of endogenously driven activity. Alternatively, behavioral differences between the two nesting groups could be a manifestation of phenotypic plasticity that arises as the hatchlings respond to unique environmental cues on each coast.     

Magnetic orientation by hatchling loggerhead sea turtles (Caretta caretta) from the Gulf of Mexico

Loggerhead sea turtle hatchlings emerge from nests on either the east or west coast of the South Florida peninsula and then migrate offshore in opposite directions. Under laboratory conditions, magnetic cues induce east coast hatchlings to swim in directions that promote their transport by oceanic surface currents, such as the North Atlantic gyre. However, the surface currents used by west coast hatchlings are unknown. We examined the responses of west (Sarasota) hatchlings to magnetic cues in the Gulf of Mexico, the Florida Straits, and the Gulf Stream to determine their (1) likely migratory routes (2) orientation where currents lead into the Atlantic Ocean, and (3) orientation adjacent to Florida’s east coast. The results suggest that migration inside Gulf waters may be circuitous, that the turtles respond appropriately to enter Atlantic waters, and that orientation along Florida’s east coast probably promotes transport by the Gulf Stream into the North Atlantic gyre.     

Locomotion performance of green turtle hatchlings from the Heron Island Rookery,Great Barrier Reef

Locomotion performance plays a vital role in determining hatchling green turtle Chelonia mydas survival in the first few hours after emerging from their nests as hatchlings crawl and swim the gauntlet of predators before reaching the relative safety of the open ocean. Previous laboratory based constant incubation experiments found incubation temperature to influence the size and swimming performance of hatchling green turtles. Here we examine the morphology and crawling and swimming performance of hatchling green turtles as they emerge from nests on Heron Island rookery in the southern Great Barrier Reef to test the hypothesis that nest temperature in the field can influence these attributes. We found inter-nest differences in hatchling mass and dimensions, and that hatchling mass was not correlated with nest temperature. However, hatchlings from warmer nests had smaller carapace dimensions than hatchlings from cool nests suggesting that more yolk was converted to hatchling tissue during embryonic development in cool nests. There was considerable intra- and inter-nest variation in both crawling and swimming performance of hatchlings. Hatchlings from cool nests tended to be faster crawlers than hatchlings from warm nests, but the thrust produced during swimming was not correlated with nest temperature. During the 4 h swimming trial, hatchlings swimming effort decreased significantly during the first 3 h but swimming effort remained relatively constant for the last 1 h. Individual hatchling crawling and swimming performances were not correlated with each other. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Discrimination of ocean wave features by hatchling loggerhead sea turtles, Caretta caretta

At the beginning of their offshore migration, hatchling sea turtles orient directly into oceanic waves as they swim away from land. Recent experiments have demonstrated that hatchlings swimming underwater can determine the propagation direction of waves by monitoring the circular movements they experience as waves pass above. During July and August 1993, we studied how loggerhead sea turtle hatchlings (Caretta caretta L.) from the east coast of Florida, USA, responded to a range of wave parameters. We constructed a wave simulator to reproduce in air the circular movements that normally occur beneath small ocean waves. Hatchlings suspended in air and subjected to these orbital movements attempted to orient into simulated waves when periods and amplitudes were similar to those found near the Florida coast. Orbital movements with longer periods (greater than 10 s), however, failed to elicit responses. The results demonstrate that hatchling loggerheads can distinguish between waves with different periods and amplitudes, and that Florida hatchlings respond most strongly to orbital movements closely resembling those of waves that occur near their natal beach. Received: 28 May 1996 / Accepted: 17 September 1996     

Nest and maternal origin can influence morphology and locomotor performance of hatchling green turtles (Chelonia mydas) incubated in field nests

In numerous laboratory experiments involving the incubation of reptile eggs, both the maternal origin of eggs and the incubating environment (nest effect) have been demonstrated to influence hatchling phenotype. Although different hatchling phenotypes have been reported from natural nests, the separate effects of maternal origin and nest on hatchling phenotype in natural nests have not been demonstrated because in natural nests the two effects are confounded with each other. Here, we use a split clutch design to experimentally separate nest effects from maternal origin effects in field nests of green turtles (Chelonia mydas). We found both maternal origin and nest to influence hatchling morphology and locomotor performance in some but not all field nests. By using egg mass (maternal origin effect) and nest temperature (nest effect) in multiple regression analysis, we found maternal origin had a greater influence than nest temperature on the morphological attributes of hatchling mass and carapace size, but nest temperature had a greater influence than maternal origin on the performance attributes of self-righting time, self-righting propensity, swim thrust during the first 30 min of swimming, and power stroke rate during the first 30 min of swimming.     

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.     

Can leftovers from predators be reliably used to monitor marine turtle hatchling sex-ratios? The implications of prey selection by ghost crabs

In marine turtles, the sex of an individual is determined by temperatures experienced during embryonic development. Gonad histological observation is still the only reliable way to determine hatchling sex, hampering the study of reproduction and of the demographic consequences of context-dependent sex-ratios, a subject of interest in a warming planet. We investigated whether hatchling remains from predation by Ocypode cursor can be used to estimate sex-ratio trends in a green turtle rookery at Poilão, Guinea-Bissau (10°52′N, 15°43′W). Sex could be readily determined in 77 and 79% of the predated hatchlings in 2008 and 2009, respectively. By comparing hatchlings killed by crabs, hatchlings accidentally dying on the reefs, and live hatchlings, we show that ghost crabs select the smaller prey, but do not select according to hatchling sex, which is explained by the lack of hatchling size dimorphism in this population. The proportion of male hatchlings was 0.45 ± 0.06 and 0.15 ± 0.06 for early and late-season clutches, respectively, these differences most likely being explained by rainfall. Using leftovers from predation by crabs may be a good solution to non-invasively monitor broad trends in sex-ratios of sea turtles.     

The effect of incubation temperature on hatchling quality in the olive ridley turtle, Lepidochelys olivacea, from Alas Purwo National Park, East Java, Indonesia: implications for hatchery management

Nest protection through egg relocation from natural nests into protected hatcheries is a common practice used at rookeries around the world to increase hatchling recruitment into sea turtle populations. However, rarely have the impacts of this practice on hatchling recruitment and quality been assessed. This study investigated the influences of the thermal nest environment of olive ridley turtles Lepidochelys olivacea on emergence success and quality of hatchlings of hatchery nests in Alas Purwo National Park, East Java, Indonesia (2009 and 2010 nesting seasons). Nest temperatures above 34?°C for at least 3 consecutive days during incubation in the hatchery resulted in decreases in emergence success and locomotor performance of hatchlings. The use of the hatchery is recommended due to extremely high predation rate of nests left on the beach; however, altering hatchery management practice by spacing nests one meter apart and providing shade should improve hatchery outcomes now and into the future.     

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.     

Influence of emergence success on the annual reproductive output of leatherback turtles

Reproductive output of leatherback turtles (Dermochelys coriacea) is affected by the stochastic nature of emergence success. Average emergence success of nests at Playa Grande, Costa Rica was 0.38 ± 0.27. Incubation temperature affected development of leatherback turtle eggs and emergence of hatchlings from the nest. We found that high temperatures reduced hatching success and emergence rate and increased embryonic mortality both early and late during incubation at Playa Grande. There was a temporal effect on emergence success that resulted in more hatchlings being produced at the beginning of the season, because of higher emergence success, than toward the end. Likewise, production of hatchlings varied from year to year. The average annual reproductive output was 252 ± 141 hatchlings per female. The 2005–2006 nesting season had the highest emergence success and produced the greatest number of hatchlings per female compared to the 2004–2005 (+120%) and 2006–2007 (+41%) seasons. However, average clutch size (62 ± 10) and clutch frequency (9.45 ± 1.63), were not different among years. Turtles that had nested a high number of years exhibited greater clutch frequency and arrived earlier to nest than turtles that had nested in fewer numbers of years. Nesting when environmental conditions favor high developmental success and emergence rate may constitute an advantageous reproductive strategy.     

Patterns in the emergence of green (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) and loggerhead (<Emphasis Type="Italic">Caretta caretta</Emphasis>) turtle hatchlings from their nests

The emergence patterns of both green (Chelonia mydas) and loggerhead (Caretta caretta) turtle hatchlings were observed in great detail over three seasons at Alagadi beach, northern Cyprus. In total, 38 green turtle and 50 loggerhead turtle nests were monitored, accounting for the emergence of 2,807 and 2,259 hatchlings, respectively. We quantified these emergences into 397 green turtle and 302 loggerhead turtle emergence groups. Overall, 85.0% of green turtle and 79.5% of loggerhead turtle groups emerged at night; these accounted for 85.5 and 90.8% of hatchlings, respectively. The remaining emergences were dispersed throughout the day for green turtle nests but confined to the morning in loggerhead turtle nests. Hatchling emergence from individual nests occurred over periods of between 1 and 7 nights, with most hatchlings typically emerging on the first night. Group sizes of green turtles emerging during the day were significantly smaller than those emerging at night. Hatchlings of both species that emerged from nests during the day had longer emergence durations than those that emerged from nests at night only.Communicated by R.J. Thompson, St. Johns     

Emergence pattern of loggerhead turtle (<Emphasis Type="Italic">Caretta caretta</Emphasis>) hatchlings from Kyparissia Bay,Greece

The present study describes the emergence pattern of loggerhead sea turtle hatchlings (Caretta caretta) from a nesting beach in Kyparissia Bay (Greece). We try to establish the role played by hatchling biometry, nest relocation and distance from nest to the sea on this emergence pattern. We surveyed a total of 32 nests, and found long emergence periods (mean = 6.7 nights). The majority of emergences occurred at night, mainly between 0030 and 0100 hours, and in small groups. Most of the hatchlings emerged from the nests the first night. We found no clear trend when we studied the effect of hatchling biometry between successive emergence days. We also found that relocation of the nests did not significantly affect the emergence pattern. However, we noted that in the relocated nests, hatchlings emerged in smaller groups. Emergence periods were inversely related to distance from the sea. In short, factors such as climate conditions, relocation and nest distance to the sea appear to have some effect on the emergence pattern. Therefore, they should be taken into account in both biological studies and management plans for sea turtle nesting beaches. Our results suggest leaving an extended period between the first emergence of hatchlings and the excavation of nests by researchers in future studies in the area.     

Foraging habitats and migration corridors utilized by a recovering subpopulation of adult female loggerhead sea turtles: implications for conservation

From 1998 to 2008, 68 adult female loggerhead sea turtles (Caretta caretta) were instrumented with platform transmitter terminals at nesting beaches in Georgia, North Carolina (NC) and South Carolina (SC) on the East Coast of the United States of America (30°48′N, 81°28′W to 33°51′N, 77°59′W). The majority of post-nesting loggerheads (N = 42, 62 %) migrated to foraging habitats in the Mid-Atlantic Bight during May–October, with a subsequent migration occurring during November–March to foraging habitats south of Cape Hatteras, NC. Nine (13 %) loggerheads initially foraged in the near-shore, coastal areas of the South Atlantic Bight, but moved to offshore habitats—closer to the Gulf Stream—during November–March, while fourteen (21 %) loggerheads remained in foraging areas along the mid-continental shelf off of the eastern coast of Florida and/or continued southward to Florida Bay and the Bahamas. The present study delineates important, post-nesting foraging habitats and migration corridors where loggerheads may interact with commercial fisheries—providing managers opportunities to develop and implement optimally effective conservation actions for the recovery of this threatened species.     

草甘膦铵盐暴露对乌龟胚胎发育、孵出幼体运动及学习表现的影响

草甘膦暴露可能对某些水生动物具有致死及亚致死毒性,但未见有涉及龟鳖类动物的行为毒理学的研究报道。用不同浓度草甘膦铵盐处理孵化中的乌龟卵来检测草甘膦暴露对其胚胎发育、孵出幼体大小、翻身能力以及空间学习能力的影响。结果表明,2～2 000 mg·L~(-1)浓度范围内的草甘膦铵盐暴露并不会影响乌龟卵孵化成功率、胚胎发育速率以及孵出个体的体质量和翻身时间,但对孵出幼体的空间学习能力产生一定影响。较高浓度的草甘膦铵盐暴露会导致孵出幼体的觅食时间延长、觅食过程中的运动距离增大。因此,胚胎期草甘膦铵盐暴露可能对乌龟孵出幼体的后续生长和存活有一定的负面效应。     

Some observations of sea turtle nesting activity in Costa Rica

Low level aerial observations were used to obtain synoptic records of the distribution of sea turtle nesting activity along both coasts of Costa Rica. Pertinent environmental information was simultaneously recorded including beach characteristics, river effluents, and evidence of coastal currents. Other correlative information was obtained from detailed maps, current charts, and climatological data. On the Caribbean coast, as expected, green turtle (Chelonia mydas) nesting was concentrated on the beaches between the Tortuguero and Parismina Rivers. On the Pacific coast, two major nesting beaches for the Pacific ridley Lepidochelys olivacea were found, each having over 100 thousand turtles aggregated offshore during the peak period between September and November. Aggregations were present at least from July through December. Massed nesting occurs each year on these same beaches and the event is known as the salida de flota by the natives of Guanacaste Province. Numerous less important nesting beaches were also found. Nesting density did not correlate well with beach quality but, instead, appeared to be related to the proximity of the beach to offshore currents. Oceanic current systems apparently facilitate the transport of sea turtles to the general vicinity of the important nesting beaches on both coasts of Coata Rica.Contribution No. 1557 from the Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, USA.     

Effects of incubation temperature on behavior of hatchling pine snakes: implications for reptilian distribution

Summary Incubation temperatures in vertebrates affect incubation periods, and in some reptiles incubation temperature determines sex ratios and some limited behavior. Here I present evidence that incubation temperature in pine snakes (Pituophis melanoleucus) affects not only incubation periods and posthatching behavior in the laboratory, but also the behavior of hatchlings required for successful emergence and survival. These behavioral differences have evolutionary implications for selection of hatchlings from particular temperature nests. With increasing temperature, incubation periods decreased in the laboratory. In addition, incubation temperature affected hatching and emergence times as well as movement speed and foraging ability. Hatchlings from medium temperature conditions emerged from nests in the field in less time than hatchlings incubated at high or low temperatures, and hatchlings from low temperatures moved slower and were less able to capture and eat mice in the laboratory than hatchlings incubated at medium or high temperatures. Taken together, these laboratory and field experiments suggest that hatchlings from low temperature nests, compared to those from higher temperature nests, would be less able to emerge, find food, and locate hibernation sites prior to the onset of cold temperatures in the New Jersey Pine Barrens. These results suggest that incubation temperature affects a whole range of behavior and that distributional ranges of reptiles and other poikilotherms could be affected by summer temperatures (via incubation period and subsequent behavior) as well as ambient winter temperatures.     

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.     

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

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

The nesting of the Pacific ridley turtle Lepidochelys olivacea on Playa Nancite,Costa Rica

A study of the nesting of the Pacific ridley turtle Lepidochelys olivacea was undertaken in Costa Rica on Playa Nancite — one of two beaches on which the authors had, the previous year, discovered large nesting aggregations of this species. During the 3 1/2-month period of this study, approximately 288,000 turtles nested on the 1300 m-long beach. About 99% of these nested during 3 periods of mass-nesting (arribadas). The predictability of the arribadas was investigated by observing and recording environmental parameters with which they may be correlated. The mass-nesting phenomenon, aspects of nesting behavior, and the adaptive advantages of mass-nesting are discussed. During the period of study, nearly 2,000 turtles were tagged, 102 of which were subsequently recovered. Carapace lengths and widths of 251 tagged turtles were measured. The emergence of hatchlings was recorded daily and, from these data, the incubation period and an indication of egg and hatchling survival was obtained. The activities of the various predators on eggs, hatchlings, and adults are described.     

Age and growth rates of Hawaiian hawksbill turtles (Eretmochelys imbricata) using skeletochronology

The Hawaiian hawksbill population has fewer than 20 females nesting per year; hence, there is a need to monitor this population closely and basic biological information on individual growth and age to maturity is critical. We present a skeletochronology analysis of Hawaiian hawksbills using humeri recovered from 30 dead stranded hawksbills, plus 10 dead hatchlings. Growth mark morphology shows readily distinguishable marks similar in appearance to other species, though some animals displayed more diffuse marks. Growth rates remained high (average 2.24–4.77 cm year^?1) from 20 to 80 cm straight carapace length (SCL). Hawksbills larger than 80 cm SCL had average growth rates of 0.3 cm year^?1. There were few adult turtles in the sample; however, results indicate hawksbills have faster growth rates than loggerhead or green turtles, with probable average age to maturity (at size 78.6 cm SCL) occurring between 17 and 22 years.