This study reviewed published data on dietary preferences of beaked whales (Ziphiidae) from stomach contents analysis. Detailed data were only available for three of the six beaked whale genera (Hyperoodon, Mesoplodon and Ziphius). Stomach samples of these three beaked whale genera primarily contained cephalopod and fish remains, although some also contained crustaceans. Mesoplodon spp. were found to contain the most fish, with some species containing nothing but fish remains, while the southern bottlenose whale (Hyperoodon planifrons) and Cuvier's beaked whale (Ziphius cavirostris) rarely, if ever, contained fish. Of cephalopods identified, Histioteuthid, Gonatid, Cranchiid and Onychoteuthid species usually contributed most to prey numbers and biomass for all beaked whale genera. There was a wide range of species and families of cephalopods recorded from stomach contents, with no obvious preference for bioluminescent prey species, vertical migrating prey species or prey species with specific body compositions. Whales of the genus Mesoplodon generally contained smaller prey, such as cephalopods under 500 g in weight, compared with other beaked whales. Hyperoodon and Ziphius frequently contained much larger cephalopods with many important prey species having a mean weight of over 1000 g. This suggests that Mesoplodon occupies a separate dietary niche from Hyperoodon and Ziphius, which may be an example of niche segregation. In contrast, Hyperoodon and Ziphius appear to occupy very similar dietary niches but have geographically segregated distributions, with Hyperoodon occupying cold-temperate to polar waters and Ziphius occupying warm-temperate to tropical waters.
This study examined sex-specific differences in home range size of adult IndoPacific bottlenose dolphins off Bunbury, Western Australia. We applied a new kernel density estimation approach that accounted for physical barriers to movements. A Bayesian mixture model was developed to estimate a sex effect in home range size with latent group partitioning constrained by association data. A post hoc analysis investigated group partitioning relating to the proportion of time spent in open vs. sheltered waters. From 2007 to 2013, photographic-identification data were collected along boat-based systematic transect lines (n = 586). Analyses focused on adult dolphins of known sex (sighted ≥ 30 times; n = 22 males and 34 females). The 95% utilization distributions of males varied between 27 and 187 km 2 ( x AE SD; 94.8 AE 48.15) and for females between 20 and 133 km 2 (65.6 AE 30.9). The mixture model indicated a 99% probability that males had larger home ranges than females. Dolphins mostly sighted in open waters had larger home ranges than those in sheltered waters. Home ranges of dolphins sighted in sheltered waters overlapped with areas of highest human activity. We suggest that sex differences in home ranges are driven by male mating strategies, and home range size differences between habitats may be influenced by prey availability and predation risk.
Skulls of odontocetes (toothed whales, including dolphins and porpoises) are typified by directional asymmetry, particularly in elements associated with the airway. Generally, it is assumed this asymmetry is related to biosonar production. However, skull asymmetry may actually be a by-product of selection pressure for an asymmetrically positioned larynx. The odontocete larynx traverses the pharynx and is held permanently in place by a ring of muscle. This allows prey swallowing while remaining underwater without risking water entering the lungs and causing injury or death. However, protrusion of the larynx through the pharynx causes a restriction around which prey must pass to reach the stomach. The larynx and associated hyoid apparatus has, therefore, been shifted to the left to provide a larger right piriform sinus (lateral pharyngeal food channel) for swallowing larger prey items. This asymmetry is reflected in the skull, particularly the dorsal openings of the nares. It is hypothesized that there is a relationship between prey size and skull asymmetry. This relationship was examined in 13 species of odontocete cetaceans from the northeast Atlantic, including four narrow-gaped genera (Mesoplodon, Ziphius, Hyperoodon, and Kogia) and eight wide-gaped genera (Phocoena, Delphinus, Stenella, Lagenorhynchus, Tursiops, Grampus, Globicephala, and Orcinus). Skulls were examined from 183 specimens to assess asymmetry of the anterior choanae. Stomach contents were examined from 294 specimens to assess prey size. Results show there is a significant positive relationship between maximum relative prey size consumed and average asymmetry relative to skull size in odontocete species (wide-gape species: R 2 ¼ 0.642, P ¼ 0.006; narrow-gape species: R 2 ¼ 0.909, P ¼ 0.031).
The level of visible (i.e. white or unpigmented) scarring on cetaceans varies greatly between species, particularly for intraspeci®c scarring in odontocete cetaceans. In some species, unpigmented intraspeci®c scars may act as an indicator of male`quality' during aggressive social interactions. Evidence to support this hypothesis was found in 18 species of odontocete cetacean. These were the narwhal (Monodon monoceros), the sperm whale (Physeter macrocephalus), the Risso's dolphin (Grampus griseus) and the family Ziphiidae (with the exception of Mesoplodon ginkgodens). The evolution of such signalling is related to the fact that teeth are not required for feeding on certain diets, primarily cephalopod-based diets, and as a result the number of teeth has been reduced. However, some teeth have been retained, and selected, as weapons for male-male competition. This has resulted in an increase in the level of intraspeci®c scarring and the greater need for a signal of`quality' to avoid costly and dangerous ®ghts. As intraspeci®c scarring became this signal, the repigmentation rate of scars was reduced, leading to all scars remaining permanently unpigmented in these species.
Cephalopods are highly sensitive to environmental conditions and changes at a range of spatial and temporal scales. Relationships documented between cephalopod stock dynamics and environmental conditions are of two main types: those concerning the geographic distribution of abundance, for which the mechanism is often unknown, and those relating to biological processes such as egg survival, growth, recruitment and migration, where mechanisms are sometimes known and in a very few cases demonstrated by experimental evidence. Cephalopods seem to respond to environmental variation both 'actively' (e.g. migrating to areas with more favoured environmental conditions for feeding or spawning) and 'passively' (growth and survival vary according to conditions experienced, passive migration with prevailing currents). Environmental effects on early life stages can affect life history characteristics (growth and maturation rates) as well as distribution and
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