To investigate the influence of temperature on the length of internesting periods in loggerhead turtles (Caretta caretta) and green turtles (Chelonia mydas), body temperature and water temperature and depth for free-ranging turtles were monitored during internesting periods using micro data loggers. Body mass and clutch size were also measured. The experiments were conducted at nesting beaches in the Japanese archipelago from 1989 through 1996. Internesting interval was significantly negatively correlated with mean body temperature and mean water temperature. Internesting intervals for some turtles exceeded 21 d when they experienced low water temperatures. Arrhenius' equation was used to describe the quantitative relationships, and Q10 values of 3.1 for water temperature and 3.4 for body temperature were calculated. There was no significant relationship between either clutch size or body mass and internesting interval. Body temperatures were kept higher than water temperatures throughout internesting periods, and larger turtles showed a higher mean thermal difference between body temperature and water temperature. The internesting interval could be considered an egg-maturation period for the next oviposition. The rate of pre-ovipositional development of eggs seemed to be accelerated by high body temperature and decelerated by low body temperature.
Summary1. Breath-hold divers are widely assumed to descend and ascend at the speed that minimizes energy expenditure per distance travelled (the cost of transport (COT)) to maximize foraging duration at depth. However, measuring COT with captive animals is difficult, and empirical support for this hypothesis is sparse. 2. We examined the scaling relationship of swim speed in free-ranging diving birds, mammals and turtles (37 species; mass range, 0AE5-90 000 kg) with phylogenetically informed statistical methods and derived the theoretical prediction for the allometric exponent under the COT hypothesis by constructing a biomechanical model. 3. Swim speed significantly increased with mass, despite considerable variations around the scaling line. The allometric exponent (0AE09) was statistically consistent with the theoretical prediction (0AE05) of the COT hypothesis. 4. Our finding suggests a previously unrecognized advantage of size in divers: larger animals swim faster and thus could travel longer distance, search larger volume of water for prey and exploit a greater range of depths during a given dive duration. 5. Furthermore, as predicted from the model, endotherms (birds and mammals) swam faster than ectotherms (turtles) for their size, suggesting that metabolic power production limits swim speed. Among endotherms, birds swam faster than mammals, which cannot be explained by the model. Reynolds numbers of small birds (<2 kg) were close to the lower limit of turbulent flow ($3 · 10 5 ), and they swam fast possibly to avoid the increased drag associated with flow transition.
A depth and temperature data logger was deployed by air gun on an individual Baird's beaked whale (Berardius bairdii) off the Pacific coast of Japan. The retrieved data logger recorded 81 dives over approximately 29 h. The maximum recorded depth and the longest dive duration were 1777 m and 64.4 min, respectively. All dives were classified into three categories by depth: deep dives (>1000 m), intermediate dives (100-1000 m), and shallow dives (<100 m). Several intermediate dives generally followed a deep dive, and sequential shallow dives followed several intermediate dives in the record of the Baird's beaked whale.
Line transect sampling is one of the most widely used methods for estimating the size of wild animal populations. An assumption in standard line transect sampling is that all the animals on the trackline are detected without fail. This assumption tends to be violated for marine mammals with surfacing/diving behaviors. The detection probability on the trackline is estimated using duplicate sightings from double-platform line transect methods. The double-platform methods, however, are insufficient to estimate the abundance of long-diving animals because these animals can be completely missed while the observers pass. We developed a more flexible hazard probability model that incorporates information on surfacing/diving patterns obtained from telemetry data. The model is based on a stochastic point process and is statistically tractable. A simulation study showed that the new model provides near-unbiased abundance estimates, whereas the traditional hazard rate and hazard probability models produce considerably biased estimates. As an illustration, we applied the model to data on the Baird's beaked whale (Berardius bairdii) in the western North Pacific.
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