Recordings of underwater vocalizations and behavioural observations were collected from 16 photographically identified resident pods of killer whales (Orcinus orca) off Vancouver Island, British Columbia, during 1978–1983. Vocalizations recorded during 43 days spent with three representative pods were analyzed for each of five activity states: foraging, travelling, group-resting, socializing, and beach-rubbing. The whales produced three types of sounds that were assumed to be social signals: discrete calls, variable calls, and aberrant calls. Discrete calls dominated vocalization in most contexts. An increase in production of variable and aberrant calls was observed during socializing and beach-rubbing activities. Each resident pod had a group-specific repertoire of 7–17 discrete call types (mean = 10.7) that was consistent over a number of years. The relative use of different calls varied with activity, but no call type was correlated exclusively with any behaviour or circumstance that could be identified. Discrete calls probably function as intragroup contact signals to maintain pod cohesion and coordinate activities. Structural modulations of standard call formats and variations in frequencies of call use appear to carry information on the emotional state of vocalizing individuals. Group-specific repertoires of calls may increase the effectiveness and reliability of this contact system and function as indicators of pod affiliation.

Underwater vocalizations were recorded during repeated encounters with 16 pods, or stable kin groups, of resident killer whales (Orcinus orca) off the coast of British Columbia. Pods were identified from unique natural markings on individuals. Vocal exchanges within pods were dominated by repetitious, discrete calls. Pods each produced 7–17 (mean 10.7) types of discrete calls. Individuals appear to acquire their pod's call repertoire by learning, and repertoires can persist with little change for over 25 years. Call repertoires differed significantly among pods in the resident population. The 16 pods formed four distinct acoustic associations, or clans, each having a unique repertoire of discrete calls, or vocal tradition. Pods within a clan shared several call types, but no sharing took place among clans. Shared calls often contained structural variations specific to each pod or group of pods in the clan. These variants and other differences in acoustic behaviour formed a system of related pod-specific dialects within the vocal tradition of each clan. Pods from different clans often travelled together, but observed patterns of social associations were often independent of acoustic relationships. It is proposed that each clan comprises related pods that have descended from a common ancestral group. New pods formed from this ancestral group through growth and matrilineal division of the lineage. The formation of new pods was accompanied by divergence of the call repertoire of the founding group. Such divergence resulted from the accumulation of errors in call learning across generations, call innovation, and call extinction. Pod-specific repertoires probably serve to enhance the efficiency of vocal communication within the group and act as behavioural indicators of pod affiliation. The striking differences among the vocal traditions of different clans suggest that each is an independent matriline.

Two forms of killer whale (Orcinus orca), resident and transient, occur sympatrically in coastal waters of British Columbia, Washington State, and southeastern Alaska. The two forms do not mix, and differ in seasonal distribution, social structure, and behaviour. These distinctions have been attributed to apparent differences in diet, although no comprehensive comparative analysis of the diets of the two forms had been undertaken. Here we present such an analysis, based on field observations of predation and on the stomach contents of stranded killer whales collected over a 20-year period. In total, 22 species of fish and 1 species of squid were documented in the diet of resident-type killer whales; 12 of these are previously unrecorded as prey of O. orca. Despite the diversity of fish species taken, resident whales have a clear preference for salmon prey. In field observations of feeding, 96% of fish taken were salmonids. Six species of salmonids were identified from prey fragments, with chinook salmon (Oncorhynchus tshawytscha) being the most common. The stomach contents of stranded residents also indicated a preference for chinook salmon. On rare occasions, resident whales were seen to harass marine mammals, but no kills were confirmed and no mammalian remains were found in the stomachs of stranded residents. Transient killer whales were observed to prey only on pinnipeds, cetaceans, and seabirds. Six mammal species were taken, with over half of observed attacks involving harbour seals (Phoca vitulina). Seabirds do not appear to represent a significant prey resource. This study thus reveals the existence of strikingly divergent prey preferences of resident and transient killer whales, which are reflected in distinctive foraging strategies and related sociobiological traits of these sympatric populations.

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We quantified the relative influence of maternal fidelity to feeding grounds and natal fidelity to breeding grounds on the population structure of humpback whales Megaptera novaeangliae based on an ocean-wide survey of mitochondrial (mt) DNA diversity in the North Pacific. For 2193 biopsy samples collected from whales in 10 feeding regions and 8 breeding regions during the winter and summer of 2004 to 2006, we first used microsatellite genotyping (average, 9.5 loci) to identify replicate samples. From sequences of the mtDNA control region (500 bp) we identified 28 unique haplotypes from 30 variable sites. Haplotype frequencies differed markedly among feeding regions (overall F ST = 0.121, Φ ST = 0.178, p < 0.0001), supporting previous evidence of strong maternal fidelity. Haplotype frequencies also differed markedly among breeding regions (overall F ST = 0.093, Φ ST = 0.106, p < 0.0001), providing evidence of strong natal fidelity. Although sex-biased dispersal was not evident, differentiation of microsatellite allele frequencies was weak compared to differentiation of mtDNA haplotypes, suggesting male-biased gene flow. Feeding and breeding regions showed significant differences in haplotype frequencies, even for regions known to be strongly connected by patterns of individual migration. Thus, the influence of migratory fidelity seems to operate somewhat independently on feeding and breeding grounds over an evolutionary time scale. This results in a complex population structure and the potential to define multiple units to conserve in either seasonal habitat.