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Marine turtle lungs have multiple functions including respiration, oxygen storage and buoyancy regulation, so lung size is an important indicator of dive performance. We determined maximum lung volumes (V(L)) for 30 individuals from three species (Caretta caretta n=13; Eretmochelys imbricata n=12; Natator depressus n=5) across a range of body masses (M(b)): 0.9 to 46 kg. V(L) was 114 ml kg(-1) and increased with M(b) with a scaling factor of 0.92. Based on these values for V(L) we demonstrated that diving capacities (assessed via aerobic dive limits) of marine turtles were potentially over-estimated when the V(L)-body mass effect was not considered (by 10 to 20% for 5 to 25 kg turtles and by >20% for turtles > or =25 kg). While aerobic dive limits scale with an exponent of 0.6, an analysis of average dive durations in free-ranging chelonian marine turtles revealed that dive duration increases with a mass exponent of 0.51, although there was considerable scatter around the regression line. While this highlights the need to determine more parameters that affect the duration-body mass relationship, our results provide a reference point for calculating oxygen storage capacities and air volumes available for buoyancy control.

Previous studies have shown that loggerhead sea turtles (Caretta caretta), monitored by satellite telemetry, complete long-distance migration between the western and eastern Mediterranean basins following a seasonal pattern. This study investigated if these migration routes may be influenced by surface currents by superimposing the tracks of three loggerhead turtles (curved carapace length >55 cm), migrating from the western to the eastern Mediterranean basin, on Lagrangian data of current developed into pseudo-eulerian speed fields. The average travel speed of the turtles was 1.6 km h−1 and did not depend on the current speed or direction. We observed a connection between surface currents and the turtles’ migration routes, although not a conclusive one. These observations show that neritic stage loggerhead turtles conduct migration in two distinct alternate phases: the first characterized by high and constant speed of travel both when swimming with or against currents and the second typified by low travel speeds and a good concurrence between the trailed routes and the course of the currents. These two phases corresponded to two types of movements, one where the turtle migrates actively to reach a specific destination (either neritic foraging, wintering or nesting ground) and the other, where the turtle drifts with the mesoscale current and forages pelagically. It seemed thus, that the influence of currents on a turtle’s movements depends on the turtle’s momentary behaviour and location of residence.

Thirteen loggerhead turtles Caretta caretta were released (10 from Naples, Italy, 2 from Monastir, Tunisia, 1 from Gallipoli, South Italy) with satellite relay data loggers (SRDL) to elucidate their overwintering behaviour. Nine turtles were successfully tracked throughout the winter, while 4 SRDLs failed to transmit after short deployment periods. Of these 9, 4 remained within 80 km of the release site, 3 travelled to a distant overwintering site, and 2 continued to move and did not remain within 80 km of a specific site. Apart from these differences, all turtles stayed near the coast and ded- icated most of their time to dives lasting 3 h and longer. Maximum dive durations ranged from 270 to 480 min and were highly correlated with water temperatures, which fell below the supposed 15°C threshold for sea turtle hibernation in all overwintering sites. Median dive depths were between 4 and 24 m and were, thus, well within the mixed layer, as revealed by temperature profiles, which also were relayed by the SRDLs. No evidence was found that the turtles preferred warmer temperatures to overwinter in, because the range of temperature was very narrow on both the horizontal and the vertical scale of their movements. Despite the long resting phases and the low temperatures (mini- mum = 11.8°C) all turtles retained activity to some degree, at least to commute between the depth of resting and the surface to breathe. While the degree of winter dormancy is certainly affected by temperature, turtles were by no means obligatory hibernators, and their ability to move and even forage during the winter may be important for their growth and maturation rates, as well as their reproductive output.

This study was performed to assess the extent to which an intermandibular angle sensor (IMASEN) may be used to elucidate the behaviour of six captive loggerhead turtles. The measuring system was glued to the beak of turtles and set to measure the intermandibular distance at 5 Hz while the turtles fed (on anchovies, squid, and live crabs), swam, rested, and breathed. The behaviour of the equipped turtles was filmed and compared afterwards to the sensor readings. The IMASEN output data allowed quantification of the number of food items ingested as well as the time between food seizure and deglutition and the type of food ingested. However, nonfeeding turtles exhibited regular jaw movements with a reduced amplitude of ca. 2.2 mm, which clearly differed from feeding movements and were caused by buccal oscillations. Such movements of the base of the buccal cavity generate a steady flow of water pass the chemosensory organs and were interrupted only during food ingestion, resting, and breathing. Breathing was clearly distinguishable by the IMASEN. The beak sensor is thus a reliable system to investigate a number of behaviours in sea turtles which encompass foraging, buccal oscillation, and respiratory frequency. It has potential for allocating time to different activities in free-ranging sea turtles and thus allows us to gain insight to their foraging and diving strategies.

Chelonian sea turtles use their lung as a buoyancy organ and as the major oxygen store when diving, and hence, buoyancy regulation and oxygen consumption can be expected to interact. The buoyancy of seven juvenile loggerhead turtles, Caretta caretta, was determined by measuring directly their underwater weight (Muw) while they were resting on a freely suspended weighing platform at a depth of 80 cm. Underwater weight was recorded continuously for 2 days for each turtle, followed by another 2 days measurements during which the turtles carried lead weights attached to their carapace, and finally, a last day of measurement after the weights had been removed. Total duration of resting dives (tr), buoyancy (FB), total resulting force acting on the resting turtle (Fres) and body volumes were derived from the Muw data. Turtles were slightly negatively buoyant when resting (Fres=−0.2943 to −0.981 N kg−1) and Muw increased significantly throughout each apnoeic period, meaning that the turtles progressively lost buoyancy. Pulmonary gas loss was calculated from the rate at which buoyancy decreased, which was significantly slower during the first half of the dive than during the second half of the dive. Resting oxygen consumption rates (VO2) were calculated from these data assuming that the pulmonary gas loss represents oxygen consumption from the lung. The VO2 obtained in this way (1.69–4.86 ml O2 min−1) corresponded well with other published and VO2 measured previously on loggerhead turtles in the same facility. Using oxygen from the lung affects buoyancy and may have impacts on the diving behaviour.

(1) We measured dorsal surface temperature (Td), skin temperature (Ts) and body temperature (Tb) of adult (white plumage) and juvenile (black plumage) Cape gannets, Morus capensis, subject to high ambient temperatures. (2) Mean Td and Tb of juveniles were significantly elevated compared to those of adults. (3) Mean Ts of older juveniles, which had down beneath their body feathers, were significantly lower than Ts of younger juveniles, indicating that the down provided insulation. (4) Juveniles spent a significantly greater proportion of time thermoregulating via evaporative cooling than adults. (5) The high thermal load of the dark plumage is presumably associated with major costs for the thermal and water balance of juveniles.

Interpretation of diving profiles of aquatic animals would be considerably enhanced by additional behavioural information. A new sensor is presented here which records animal movements. This sensor was tested on a captive loggerhead turtle Caretta caretta which showed similar activity patterns to free-living green turtles Chelonia mydas. A computer program with user-selectable options was developed to analyse the data consistently and rapidly. Using our sensor we calculated the total resting time, which differed by less than 5% from the real resting time when the sampling interval was 2 s. The method was additionally tested for different sampling intervals to find out its applicability for field studies.

Diving reptiles, unlike most diving birds and mammals, return infrequently to the surface to breathe. Spending the bulk of their lives underwater, they are likely to have developed a large variety of specific behavioural patterns different from those of their warm-blooded counterparts. However, for technical reasons, underwater behaviour of these aquatic reptiles remains poorly understood. In this study green turtles Chelonia mydas nesting on Cyprus (Eastern Mediterranean) were equipped with multi-channel data loggers monitoring diving behaviour and activity (via a logger-integrated 3-D compass which served as an activity sensor) during the inter-nesting interval. Data from 2 turtles for 2 consecutive inter-nesting intervals were available for detailed dive analysis. Both turtles showed highly variable dive patterns ranging from travelling subsurface dives to specific dive types such as U- (mainly resting and foraging dives), S- (a form of energy saving swimming) and V-dives. The green turtles stayed near the coast throughout the study, dived no deeper than ca 25 m, but remained underwater for up to ca 40 min. The recordings of the activity sensor revealed high activity levels (less than 20% resting d -1 ) during the whole inter-nesting period which was attributed to extensive foraging. The combination of both the activity data and the dive data showed that the turtles were engaged in travelling movements for 46 % of the inter-nesting time spent underwater, foraged for 34 % and rested for 12% of the time. We discuss the physiological, ecological and conservation implications of these results.

""Several studies investigated how changes in bone density are related to the evolution of complex buoyancy control systems in aquatic mammals. Very little is known on sea turtles, although this is one of the most ancient tetrapod groups that successfully colonized the marine environments. Here, we investigated for the first time the relationship between bone density and body size in the loggerhead turtle, Caretta caretta, with the aim to elucidate possible functional connections with the species’ aquatic habits. Humeri were extracted from the carcasses of 72 loggerhead turtles ranging in size from 7 to 89 cm (males = 18, females = 44, unknown = 10). Whole bone density was determined by Archimedes’ principle. Sexes exhibited comparable humerus densities (t-value = 0.49, P > 0.05). Mean humerus density (1.33 g cm−3) was intermediate within the range reported for marine mammals and suggested no extreme specialization towards an either pelagic or benthic lifestyle. Turtle size and humerus density were significantly correlated (Pearson's correlation = 0.638, P < 0.01). Small juveniles had very light bones compared to adults in accordance with their stage specific pelagic diving and foraging behaviour.""

Divergent selection in mice on fatness over 60 generations produced a fat (F) and a lean (L) line, having about 22% and 4% body fat, respectively. To elucidate the importance of the leptin regulatory feedback loop in the genetic changes produced by this selection, Lep(ob) and Lepr(db) mutations causing leptin production and leptin receptor deficiency, respectively, were introgressed individually into both lines by repeated backcrossing. The fat amount increased significantly in homozygotes for Lep(ob) or Lepr(db) in both lines, for example, in F and L males from 8.5 to 18.8 and 17.2 g (P

SUMMARYMarine 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°C to 10.5°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.

A group of approximately 370 Egyptian tortoises (Testudo kleinmanni) and 36 spur-thighed tortoises (Testudo graeca) were illegally imported into Italy from Libya. Within 6 mo of their entry into Italy, all but 40 of the Egyptian tortoises had died with signs of severe stomatitis. Herpesviruses were detected from the tongues of seven Egyptian tortoises by polymerase chain reaction (PCR) and virus isolation. Sequencing of a portion of the UL39 homologue of the herpesviruses from three different tortoises demonstrated that the viruses were identical to one another and identical to a herpesvirus isolated from a Hermann's tortoise (Testudo hermanni) in Germany. This is the first description of the detection of a herpesvirus from diseased Egyptian tortoises. That these animals were imported into Europe from Libya provides circumstantial evidence for the presence of herpesviruses among tortoises in northern Africa.

A loggerhead turtle nest was accidentally discovered during the raking of a beach at St Tropez, France, on 18 July 2006. This is the northernmost loggerhead nest so far in the Mediterranean and in the world. The clutch was deposited close to the sea in a sand-soil-pebbles mixture and became partially inundated in September. In total there were 141 eggs, none of which hatched. Only 24% of the eggs contained embryos, while 107 eggs contained yolk but no visible embryo. The failure to hatch was probably the result of the non-suitable nest environment, the low mean incubation temperatures and the inundation. Further observations of beaches are recommended to establish other nesting occurrences of loggerhead turtles in this region.

Here we report for the first time on a loggerhead turtle, Caretta caretta, which laid 92 eggs on the south-west Italian coast on 11 July 2002. During the 64 day incubation period the nest was threatened by inundation and hence, it was transferred on the 28th day. The hatching success was 49.4% and all live hatchlings entered the sea. Unhatched eggs were opened to determine at which developmental stage embryonic death occurred. This analysis confirmed that most of the embryos died in the first few days after laying and that the transfer of the nest did not affect embryonic development. This was the third of three unusual nesting events in the western Mediterranean in the years 2001–2002.

The first published record, from the early 1970s, of hibernation in sea turtles is based on the reports of the indigenous Indians and fishermen from Mexico, who hunted dormant green turtles ( Chelonia mydas ) in the Gulf of California. However, there were no successful attempts to investigate the biology of this particular behaviour further. Hence, data such as the exact duration and energetic requirements of dormant winter submergences are lacking. We used new satellite relay data loggers to obtain the first records of up to 7 h long dives of a loggerhead turtle ( Caretta caretta ) overwintering in Greek waters. These represent the longest dives ever reported for a diving marine vertebrate. There is strong evidence that the dives were aerobic, because the turtle surfaced only for short intervals and before the calculated oxygen stores were depleted. This evidence suggests that the common belief that sea turtles hibernate underwater, as some freshwater turtles do, is incorrect.

We monitored oxygen consumption (VO2), body temperatures (Tb), submersion intervals, and circadian rhythms of VO2 in nine loggerhead turtles during a 6-mo period. The turtles originated from the Tyrhennian Sea, South Italy (40 degrees 51'N, 14 degrees 17'E) and were kept in indoor tanks at constant photoperiod while being subject to the seasonal decline in water temperature (Tw=27.1 degrees to 15.3 degrees C). From summer to winter, all turtles underwent profound reductions in VO2 (Q10=5.4). Simultaneously, their activity was greatly reduced and submergence intervals increased. Over 24-h periods, however, the turtles showed no circadian rhythm in activity or VO2. However, there was a significant positive correlation between the proportion of a day spent actively swimming and VO2. Tb's were not significantly different from Tw and followed the same seasonal decline. A second experiment was conducted to establish the effect of short-term exposure to various temperatures on VO2. Tb equilibrated with the experimental Tw within 3 h. The metabolic responses were again positively correlated with changes in Tw, but this time the corresponding Q10 was only 1.3. On the basis of the range of body masses of the turtles used in this study (2-60 kg), the intraspecific scaling exponent for VO2 was 0.353.

Divergent selection in mice on fatness over 60 generations produced a fat (F) and a lean (L) line, having about 22% and 4% body fat, respectively. To elucidate the importance of the leptin regulatory feedback loop in the genetic changes produced by this selection, Lep(ob) and Lepr(db) mutations causing leptin production and leptin receptor deficiency, respectively, were introgressed individually into both lines by repeated backcrossing. The fat amount increased significantly in homozygotes for Lep(ob) or Lepr(db) in both lines, for example, in F and L males from 8.5 to 18.8 and 17.2 g (P0.001) and from 1.25 to 18.0 and 12.7 g (P0.001), respectively. Line differences were, however, mostly maintained after introgression. Concentrations of circulating leptin were relatively independent of the original lines but heavily dependent on the introgressed genotype. Introgression of leptin production and receptor deficiencies had separate effects from long-term selection, indicating that the genes responsible for the line divergence must act independently of the leptin regulatory system. Energy budget analysis indicated that the major line differences were in the level of energy expended on physical activity, and these differences were preserved following introgression, suggesting that multiple pathways regulate fatness, which may be independently responsive to intervention.

Despite substantial knowledge on thermoregulation in reptiles, the mechanisms involved in heat exchange of sea turtles have not been investigated in detail. We studied blood flow in the front flippers of two green turtles, Chelonia mydas, and four loggerhead turtles, Caretta caretta, using Doppler ultrasound to assess the importance of regional blood flow in temperature regulation. Mean blood flow velocity and heart rate were determined for the water temperature at which the turtles were acclimated (19.3 degrees-22.5 degrees C) and for several experimental water temperatures (17 degrees-32 degrees C) to which the turtles were exposed for a short time. Flipper circulation increased with increasing water temperature, whereas during cooling, flipper circulation was greatly reduced. Heart rate was also positively correlated with water temperature; however, there were large variations between individual heart rate responses. Body temperatures, which were additionally determined for the two green turtles and six loggerhead turtles, increased faster during heating than during cooling. Heating rates were positively correlated with the difference between acclimation and experimental temperature and negatively correlated with body mass. Our data suggest that by varying circulation of the front flippers, turtles are capable of either transporting heat quickly into the body or retaining heat inside the body, depending on the prevailing thermal demands.

Hochscheid et al. (1999) used time-depth recorders(TDRs) and activity recorders (Hochscheid & Wilson1999) to examine diving behaviour and activity ofgreen turtles during their internesting period atCyprus. Turtles were found to spend a large propor-tion of time undertaking dives with a characteristic‘U-shaped’ profile, i.e. dives where individuals re-mained at a fixed depth for a long period, surfacedbriefly and then descended to the same depth again.Information from the activity sensor suggested thatsome of these U-dives were associated with resting,others with benthic activity.While TDRs have been extensively deployed onmarine mammals and birds, their deployment on seaturtles is still in its infancy. We are only now starting toappreciate the wealth of information that these instru-ments can provide about free-living turtles. Unlikemany marine mammals, shallow diving marine tur-tles—such as the green