Enhanced oxygen reserves in the blood facilitate diving in marine mammals. For pinnipeds (seals and sea lions), a developmental period of 4 to 24 months is required for blood oxygen stores to reach adult capacities. We investigated whether a similar developmental period for the blood occurs in cetaceans (dolphins and whales), a group of mammals that are exposed to diving immediately after birth. Blood samples were collected from wild and zoological park bottlenose dolphins Tursiops truncatus aged 0±12 years. Red blood cell number (RBC), haemoglobin content (Hb), haematocrit (Hct), mean corpuscular volume (MCV), mean cell haemoglobin (MCH), and mean corpuscular haemoglobin concentration (MCHC) were determined for each sample. We found that during postnatal development, RBC, Hb and Hct decreased from 0 to 1.5 months and then increased from 1.5 to 6 months, reaching adult levels by 3 years. MCV and MCH both increased from birth. MCHC decreased from 0 to 3.2 months and then increased. Adult levels for MCV were attained as early as 2 months of age while adult levels for MCH and MCHC were attained by 6 months of age. These results indicate that, for bottlenose dolphins, the development of the blood and its capacity to store oxygen is not complete with weaning, which generally occurs at 1.5 years old. The lower oxygen storage capacity of immature dolphins is likely to limit dive capabilities. Calculated aerobic dive limits (cADLs) for 0-to 2-year-old dolphin calves are 1.9±3.6 min, compared to 4.8±5.4 min for 3-to 12-year-old dolphins. Increases in cADLs from 0 to 3 years are attributed to increases in both body mass and mass speci®c oxygen stores while body mass alone explains the increases in cADLs from 3 to 9 years. The limited diving capacity of young dolphins may in¯uence the foraging behaviours of newly weaned juveniles and females accompanied by calves.

Phylogenetic analysis of novel dolphin (Tursiops truncatus) papillomavirus sequences, TtPV1, -2, and -3, indicates that the early and late protein coding regions of their genomes differ in evolutionary history. Sliding window bootscan analysis showed a significant a change in phylogenetic clustering, in which the grouped sequences of TtPV1 and -3 move from a cluster with the Phocoena spinipinnis PsPV1 in the early region to a cluster with TtPV2 in the late region. This provides indications for a possible recombination event near the end of E2/beginning of L2. A second possible recombination site could be located near the end of L1, in the upstream regulatory region. Selection analysis by using maximum likelihood models of codon substitutions ruled out the possibility of intense selective pressure, acting asymmetrically on the viral genomes, as an alternative explanation for the observed difference in evolutionary history between the early and late genomic regions of these cetacean papillomaviruses.

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Ultrasonographic measurements were made at least once a month during 14 gestations in seven Tursiops truncatus and 12 gestations in five Tursiops aduncus (bottlenosed dolphins). The 121 measurements of the fetal biparietal diameter and 139 measurements of the fetal thoracic diameter in T truncatus and the 97 measurements of the biparietal diameter and 97 measurements of the thoracic diameter in Taduncus were used to establish regression lines for the increases in the diameter of the head and thorax of the fetus with time. From these relationships an easy-to-use computer program was developed to predict the date of birth of the two species of bottlenosed dolphin, and its predictions were compared with the actual dates of birth of other calves of both species. The births occurred within the range of predicted dates, and even when only a few measurements were available, the program provided accurate predictions.

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