Free-ranging Loggerhead Turtles Research Articles

Heart rate as a proxy for estimating oxygen consumption rates in loggerhead turtles (Caretta caretta).

ABSTRACTHeart rates of air-breathing diving animals can change on a short time scale due to the diving response during submergence. Heart rate is used frequently as a proxy for indirectly estimating metabolic rates on a fine time scale. However, most studies to date have been conducted on endothermic diving animals, and the relationships between metabolic rates and heart rates in ectothermic diving animals have not been well studied. Sea turtles are unique model organisms of diving ectotherms because they spend most of their life in the ocean and perform deep and/or long dives. In this study, we examined the relationship between heart rates and metabolic rates in captive loggerhead turtles, Caretta caretta, to estimate oxygen consumption rates during each dive based on heart rates. The oxygen consumption rates (V̇O2: mlO2 min−1 kg−1) and average heart rates (fH: beats min−1) were measured simultaneously in indoor tanks at water temperatures of 15–25°C. Our results showed that oxygen consumption rate was affected by heart rate and water temperature in loggerhead turtles. Based on the collected data, we formulated the model equation as V̇O2=0.0124fH+0.0047Tw - 0.0791. The equation can be used for estimating fine-scaled field metabolic rates in free-ranging loggerhead turtles. The results of this study will contribute to future comparative studies of the physiological states of ectothermic diving animals.

Body temperature stability achieved by the large body mass of sea turtles.

To investigate the thermal characteristics of large reptiles living in water, temperature data were continuously recorded from 16 free-ranging loggerhead turtles, Caretta caretta, during internesting periods using data loggers. Core body temperatures were 0.7-1.7°C higher than ambient water temperatures and were kept relatively constant. Unsteady numerical simulations using a spherical thermodynamic model provided mechanistic explanations for these phenomena, and the body temperature responses to fluctuating water temperature can be simply explained by a large body mass with a constant thermal diffusivity and a heat production rate rather than physiological thermoregulation. By contrast, body temperatures increased 2.6-5.1°C in 107-152 min during their emergences to nest on land. The estimated heat production rates on land were 7.4-10.5 times the calculated values in the sea. The theoretical prediction that temperature difference between body and water temperatures would increase according to the body size was confirmed by empirical data recorded from several species of sea turtles. Comparing previously reported data, the internesting intervals of leatherback, green and loggerhead turtles were shorter when the body temperatures were higher. Sea turtles seem to benefit from a passive thermoregulatory strategy, which depends primarily on the physical attributes of their large body masses.

When surfacers do not dive: multiple significance of extended surface times in marine turtles

Marine turtles spend more than 90% of their life underwater and have been termed surfacers as opposed to divers. Nonetheless turtles have been reported occasionally to float motionless at the surface but the reasons for this behaviour are not clear. We investigated the location, timing and duration of extended surface times (ESTs) in 10 free-ranging loggerhead turtles (Caretta caretta) and the possible relationship to water temperature and diving activity recorded via satellite relay data loggers for 101-450 days. For one turtle that dived only in offshore areas, ESTs contributed 12% of the time whereas for the other turtles ESTs contributed 0.4-1.8% of the time. ESTs lasted on average 90 min but were mostly infrequent and irregular, excluding the involvement of a fundamental regulatory function. However, 82% of the ESTs occurred during daylight, mostly around noon, suggesting a dependence on solar radiation. For three turtles, there was an appreciable (7 degrees C to 10.5 degrees C) temperature decrease with depth for dives during periods when ESTs occurred frequently, suggesting a re-warming function of EST to compensate for decreased body temperatures, possibly to enhance digestive efficiency. A positive correlation between body mass and EST duration supported this explanation. By contrast, night-active turtles that exceeded their calculated aerobic dive limits in 7.6-16% of the dives engaged in nocturnal ESTs, probably for lactate clearance. This is the first evidence that loggerhead turtles may refrain from diving for at least two reasons, either to absorb solar radiation or to recover from anaerobic activity.

Sea turtles compensate deflection of heading at the sea surface during directional travel

Air-breathing marine animals, including sea turtles, utilise two fundamentally different environments (i.e. sea surface and underwater) during migration. Many satellite telemetry studies have shown travel paths at relatively large spatio-temporal scales, discussing the orientation and navigation mechanisms that guide turtles. However, as travel paths obtained by satellite telemetry only reflect movements at the surface, little is known about movements and orientation ability underwater. In this study, to assess orientation ability both at the surface and underwater, fine-scale 3-D movements of free-ranging loggerhead turtles Caretta caretta were reconstructed by using multi-sensor data loggers. Video systems ('Crittercam') were also used to record the behaviour of the turtles and the visual information surrounding the turtles. During August and October in 2006 and 2007, eight turtles were released from Otsuchi Bay, Japan (39 degrees 20'30N, 141 degrees 56'00E), and a total of 118 h of 3-D movements were reconstructed. Turtles maintained highly straight-line courses (straightness index >0.95) during 41% of the total duration (i.e. 'travelling periods'). During travelling periods, turtles swam continuously, maintaining unidirectional heading throughout dives whereas turtles changed heading remarkably at the surface. Despite highly directional movements during dives, travel direction tended to shift by the end of dives lasting 10 minutes or more. Such deflections seemed to be compensated during subsequent surfacing periods because there was a negative relationship between changes in travel direction arising during dives and subsequent surfacing periods. Therefore, remarkable changes in heading at the surface could be interpreted as direction-searching behaviour. Our results suggested that turtles undertaking directional travel were more dependent on directional information that was reliable at the surface.

Body temperature independence of solar radiation in free-ranging loggerhead turtles, Caretta caretta, during internesting periods

Body temperatures, ambient water temperatures, light intensities and vertical positions (depth) of eight loggerhead turtles, Caretta caretta, were monitored by small recorders during internesting periods from 1991 through 1993 off Wakayama Prefecture, Japan. Body temperatures of eight loggerhead turtles were higher than ambient water temperatures through-out their internesting periods. Light intensities were compared with body temperatures and no evidence was obtained to suggest that the raised body temperatures were caused by the direct influence of solar radiation. Body temperatures were kept higher than water temperatures in cloudy weather or even at night. Mean thermal differences between body and water temperatures were significantly different among individuals, and larger turtles had a greater mean thermal difference. Elevations in body temperatures of adult loggerhead turtles can reasonably be assumed to result from the accumulation of metabolically produced heat. Surfacing times (spent at depths shallower than 2 m) of seven turtles were only 10.3 to 38.9% of their internesting periods, with the exception of one turtle who spent 66.3% of her time at the surface. Loggerhead turtles did not seem to bask positively at the sea surface to absorb radiative heat.

Correlation between stomach temperatures and ambient water temperatures in free-ranging loggerhead turtles, Caretta caretta

Instruments were attached to loggerhead turtles, Caretta caretta, at Kamoda Point, Japan in 1989 and on the Senri-coast, Japan in 1991. We simultaneously obtained stomach temperatures, ambient water temperatures and diving depths from four free-ranging loggerhead turtles during the internesting periods, using small recorders. These data were analyzed to understand how body temperature was maintained. Ambient water temperatures changed coincidentally when turtles moved up or down, but a stable stomach temperatures was maintained despite water temperature fluctuations of ca. 20 to 90 min in duration. Loggerhead turtles also experienced water temperature fluctuations longer than 24 h. Stomach temperatures responded to those water temperature changes with a time lag of several hours (160, 170, 230 and 240 min). Stomach temperatures were higher than ambient water temperatures throughout the experimental periods. The median values of the thermal difference between stomach and water temperatures were 1.1, 1.3, 1.5 and 1.7°C. The higher stomach temperatures are thought to be caused by metabolic heat production.