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Navigation and seasonal migratory orientation in juvenile sea turtles.

Juvenile loggerhead and green turtles that inhabit inshore waters of North Carolina, USA undertake long seasonal migrations, after which they often return to specific feeding areas. In addition, juvenile turtles are capable of homing to specific sites after being displaced. As a first step towards investigating the navigational mechanisms that underlie these movements, juvenile turtles were captured in coastal waters of North Carolina and displaced 30-167 km along circuitous routes while deprived of visual cues. At the testing location, turtles were tethered in a circular arena and permitted to swim while their orientation was monitored. Between May and September, when juvenile loggerhead and green turtles inhabit feeding areas along the North Carolina coast, turtles oriented in directions that corresponded closely with the most direct route back to their capture locations. During October and November, however, both loggerhead and green turtles oriented southward, a direction consistent with the migratory paths of turtles beginning their autumn migration. The results demonstrate for the first time that both homing and migratory orientation can be elicited in juvenile turtles under laboratory conditions in which orientation cues can be readily manipulated. In addition, the results provide evidence that juvenile loggerheads can assess their position relative to a goal using local cues available at the test site and are therefore capable of map-based navigation.

Animal Migration↗

Open-sea migration of magnetically disturbed sea turtles.

Green turtles (Chelonia mydas) that shuttle between their Brazilian feeding grounds and nesting beaches at Ascension Island in the middle of the Atlantic Ocean are a paradigmatic case of long-distance oceanic migrants. It has been suggested that they calculate their position and the direction of their target areas by using the inclination and intensity of the earth's magnetic field. To test this hypothesis, we tracked, by satellite, green turtles during their postnesting migration from Ascension Island to the Brazilian coast more than 2000 km away. Seven turtles were each fitted with six powerful static magnets attached in such a way as to produce variable artificial fields around the turtle that made reliance on a geomagnetic map impossible. The reconstructed courses were very similar to those of eight turtles without magnets that were tracked over the same period and in the previous year, and no differences between magnetically disrupted and untreated turtles were found as regards navigational performance and course straightness. These findings show that magnetic cues are not essential to turtles making the return trip to the Brazilian coast. The navigational mechanisms used by these turtles remain enigmatic.

Animals↗

Energetics of swimming of a sea turtle.

Young (mean mass 735 g) green turtles (Chelonia mydas) were able to swim in a water channel at sustained speeds between 0-14 and 0-35 m.s-1. Oxygen consumption at rest was was 0-07 l.kg-1.h-1; at maximum swimming speed oxygen consumption was 3-4 times greater than at rest for a given individual. In comparison with other animals of the same body mass the cost of transport for the green turtle (0.186lO2.kg-1.km-1) is less than that for flying birds but greater than that for fish. From drag measurements it was calculated that the aerobic efficiency of swimming was between 1 and 10%; the higher efficiencies were found at the higher swimming speeds. Based upon the drag calculations for young turtles, it is estimated that adult turtles making the round-trip breeding migration between Brazil and Ascension Island (4800 km) would require the equivalent of about 21% of their body mass in fat stores to account for the energetic cost of swimming.

Aerobiosis↗

An analysis of the growth based on the size and age distributions of the hawksbill sea turtle inhabiting Cuban waters.

The first costal scute (C 1) collected from 2, 749 hawksbill turtle (Eretmochelys imbricata) captured in Cuban waters in 1993 and 1994 were analyzed to determine their body size and age distributions. The C 1 width (C 1 W) was converted to the straight carapace length (SCL) using a formula, SCL = 4.3527 (C 1 W)0.8484, to examine its body size distribution. The SCL ranged from 51.3 to 96.1 cm with 68.8 cm of mean and 68.6 cm of median. Ages of captured turtles estimated from the C 1 surface patterns were ranged from 3.3 to 61.5 years old with 15.8 years of mean and 14.5 years of median. A growth function of van Bertalanffy, M(t) = A(1-Be-kt), was applied to determine the relationship between the age and body size (SCL). A formula, SCL = 80.4(1 -0.663e-0.118(Age)), was derived and indicated a slowdown in the growth after about 14 years old. The maturation age and the rate of sexually matured Cuban hawksbill turtles were also discussed based on these results.

Age Distribution↗

Organochlorine residues in eggs of loggerhead and green sea turtles nesting at Merritt Island, Florida--July and August 1976.

Eggs from nine clutches of loggerhead turtles (Caretta caretta) and two clutches of green turtles (Chelonia mydas) were collected as they were laid on Merritt Island, Florida. Eggs were incubated, frozen, and analyzed for organochlorines. Levels of DDE and PCB, the major contaminants, averaged less than 0.08 ppm in loggerhead eggs and were even lower in green turtle eggs. These concentrations are far below levels thought to be potentially harmful. Loggerhead eggs were frozen after 43-52 days incubation; both DDE and PCB declined significantly during this interval. Authors estimate that DDE averaged about 0.2 ppm in loggerhead eggs when they were laid. DDE levels in eggs of both turtle species were less than levels in eggs of crocodiles (Crocodylus acutus) from Everglades National Park and in eggs of 13 species of aquatic birds nesting on Merritt Island. The remarkably low residues in the turtle eggs probably indicate that, when not nesting, the turtles live and feed in areas remote from Florida.

Animals↗

Exercise warms adult leatherback turtles.

Leatherback sea turtles (Dermochelys coriacea) can maintain body temperature (T(B)) up to 18 degrees C above that of the surrounding sea water (T(W)) which allows leatherbacks to enter cold temperate waters and have the largest global range of any reptile. Using a cylindrical model of a leatherback we investigated the extent to which heat production through variation of swim speed could be used in a leatherback's thermal strategy. Drag force of a full scale cast of a leatherback was measured in a low velocity wind tunnel to obtain an estimate of the metabolic cost needed to offset drag. Heat released in the core of a turtle as a byproduct of the metabolic cost of locomotion is conducted from the core of the turtle to the surrounding water through its insulation layer. By keeping insulation thickness constant, we highlight the effectiveness of swim speed in maintaining T(B)-T(W). Our model, when tested against published data at a given T(W), showed a close correlation between predicted and measured swimming speed at a given T(B). We conclude that the ability to maintain a large T(B)-T(W) is an interplay between mass, insulation thickness and water temperature selection but behavioural control of swimming speed predominates.

Animals↗

Distorting gene pools by conservation: Assessing the case of doomed turtle eggs.

Sea turtles have a high reproductive output and high mortality at early stages of the life cycle. In particular, many nests are laid below or close to high tide lines, and subsequently large numbers of eggs may be inundated and destroyed. A common conservation procedure is to relocate such doomed eggs to higher ground. This article examines this practice in the light of recent data revealing that some individual turtles tend to nest relatively near the water and others relatively higher up the beach. Discussion is focused on the question of why apparently poor placement of nests has not been selected against. Comparison between the ecology of leatherback and hawksbill turtle nesting beaches suggests that predictability of environmental conditions on the nesting beaches has an important influence on patterns of nest-site selection. Options are outlined for the management of nesting beaches where a high proportion of turtle eggs is subject to destruction by flooding.

Animals↗

Circulating serotonin in vertebrates.

The role of circulating serotonin is unclear and whether or not serotonin is present in the blood of non-mammalian species is not known. This study provides the first evidence for the presence of serotonin in thrombocytes of birds and three reptilian species, the endothermic leatherback sea turtle, the green sea turtle and the partially endothermic American alligator. Thrombocytes from a fresh water turtle, American bullfrog, Yellowfin tuna, and Chinook salmon did not contain serotonin. Serotonin is a vasoactive substance that regulates skin blood flow, a major mechanism for endothermic body temperature regulation, which could explain why circulating serotonin is present in warm-blooded species. The temperature sensitivity of human blood platelets with concomitant changes in serotonin content further supports a link between circulating serotonin and thermoregulation. Phylogenetic comparison of the presence of circulating serotonin indicated an evolutionary divergence within reptilian species that might coincide with the emergence of endothermy.

Alligators and Crocodiles↗