Ecological and social determinants of group size in transient killer whales

Most analyses of the relationship between group size and foodintake of social carnivores have shown a discrepancy betweenthe group size that maximizes energy intake and that which ismost frequently observed. Around southern Vancouver Island,British Columbia, killer whales of the so-called transient formforage in small groups, and appear to prey exclusively on marinemammals. Between 1986 and 1993, in approximately 434 h of observationson transient killer whales, we observed 138 attacks on fivespecies of marine mammals. Harbor seals were most frequentlyattacked (130 occasions), and the observed average energy intakerate was more than sufficient for the whale's energetic needs.Energy intake varied with group size, with groups of three havingthe highest energy intake rate per individual. While groupsof three were most frequently encountered, the group size experiencedby an average individual in the population (i.e., typical groupsize) is larger than three. However, comparisons between observedand expected group sizes should utilize only groups engagedin the behavior of interest. The typical size of groups consistingonly of adult and subadult whales that were engaged primarilyin foraging activities confirms that these individuals are foundin groups that are consistent with the maximization of energyintake hypothesis. Larger groups may form for (1) the occasionalhunting of prey other than harbor seals, for which the optimalforaging group size is probably larger than three; and (2) theprotection of calves and other social functions. Key words:dispersal, foraging, group hunting, harbor seals, killer whales,optimal group size, social structure. [Behav Ecol 7: 408-416(1996)]     

POPULATION CHARACTERISTICS AND MIGRATION OF SUMMER AND LATE-SEASON HUMPBACK WHALES (MEGAPTERA NOVAEANGLIAE) IN SOUTHEASTERN ALASKA

A total of 326 humpback whales (Megaptera novaeangliae) were individually identified in southeastern Alaska during five summer seasons (July to September) and four late seasons (November to February) spanning the years 1979 to 1983. Peak numbers of whales were found late in August or early in September. Whales arrived 1–2 wk later in 1982 than in 1981. Whales sighted in both the summer and late seasons of 1981 and 1982 remained about 3.7 mo and one whale remained for at least 4.9 mo. Humpback whales from southeastern Alaska wintered in Hawaiian or Mexican waters, but generally did not travel to other feeding regions. The most rapid migratory transit between Hawaii and southeastern Alaska was 79 d. Based on mark-recapture analyses of the photographic data, we estimate a population of 270–372 whales in the southeastern Alaska feeding herd.     

Dietary habits of polar bears in Foxe Basin,Canada: possible evidence of a trophic regime shift mediated by a new top predator

Polar bear (Ursus maritimus) subpopulations in several areas with seasonal sea ice regimes have shown declines in body condition, reproductive rates, or abundance as a result of declining sea ice habitat. In the Foxe Basin region of Nunavut, Canada, the size of the polar bear subpopulation has remained largely stable over the past 20 years, despite concurrent declines in sea ice habitat. We used fatty acid analysis to examine polar bear feeding habits in Foxe Basin and thus potentially identify ecological factors contributing to population stability. Adipose tissue samples were collected from 103 polar bears harvested during 2010–2012. Polar bear diet composition varied spatially within the region with ringed seal (Pusa hispida) comprising the primary prey in northern and southern Foxe Basin, whereas polar bears in Hudson Strait consumed equal proportions of ringed seal and harp seal (Pagophilus groenlandicus). Walrus (Odobenus rosmarus) consumption was highest in northern Foxe Basin, a trend driven by the ability of adult male bears to capture large‐bodied prey. Importantly, bowhead whale (Balaena mysticetus) contributed to polar bear diets in all areas and all age and sex classes. Bowhead carcasses resulting from killer whale (Orcinus orca) predation and subsistence harvest potentially provide an important supplementary food source for polar bears during the ice‐free period. Our results suggest that the increasing abundance of killer whales and bowhead whales in the region could be indirectly contributing to improved polar bear foraging success despite declining sea ice habitat. However, this indirect interaction between top predators may be temporary if continued sea ice declines eventually severely limit on‐ice feeding opportunities for polar bears.     

First record of humpback whale songs in Southern Chile: Analysis of seasonal and diel variation

Male humpback whales (Megaptera novaeangliae) produce complex, patterned songs that are traditionally recorded on their breeding grounds. In this work, we report results from the first continuous acoustic monitoring of a humpback whale feeding ground off southern Chile, Corcovado Gulf. Using an autonomous continuously recording system anchored to the seafloor and an automatic signal detector, we used the units within a song to analyze the temporal distribution and diel patterns of humpback whales. Acoustic recordings were made at the end of the austral summer and autumn of 2012. Songs occurred over the entire 130 d monitoring period, from 1 February to 15 June 2012. The percentage of units detected increased throughout the monitored period with the highest detections in the last recorded month (June), despite recording for fewer days that month. Furthermore, songs were detected during all light regimes studied, but most frequently during darkness. This study provides further evidence that, far from being rare or sporadic, humpback whale songs occur commonly at a feeding ground in high latitudes over different light conditions and in all months, with a peak in autumn.     

TRENDS IN THE INSHORE RIGHT WHALE POPULATION OFF SOUTH AFRICA, 1969–1987

Results of annual aerial surveys of the right whale population along the southern coast of South Africa from 1971 to 1987 are analysed. About 91.5% of cows with calves and 82% of unaccompanied adults on the South African coast in spring are found within the standard survey area, with some indications that the range is expanding up the west coast. In the nearshore region, most right whales (90%) are found within 1.85 km, and all cows with calves within 0.93 km, of the coast. Within the standard survey area, specific areas of concentration can be predictably identified, both for cows with calves and unaccompanied adults. Although total counts (and counts expressed per hour flown) have increased overall, by a best estimate of 6.8% (95% CL 4.6, 9.0) per year from 1971 to 1987, some concentration areas for both classes have failed to show an increase over the same time period. Photographic flights since 1979 have permitted the movements of individually identified adult females to be monitored between successive calves. In at least one concentration area for which no overall increase between 1971 and 1987 was apparent (Mossel Bay), a large net emigration rate was found, nearly all of which involved a shift to the main nursery area to the west, off De Hoop. Reasons for the dissimilar dynamics of different concentration areas are not yet known.     

Assessment of mark–recapture models to estimate the abundance of a humpback whale feeding aggregation in Southeast Alaska

Aim The aim of this study was to use photographs of the unique pattern on the ventral surface of the flukes to estimate the abundance of humpback whales (Megaptera novaeangliae) in a discrete feeding aggregation in northern Southeast Alaska. Location The study was located in northern Southeast Alaska, USA, in the eastern North Pacific Ocean. Methods This study evaluated mark–recapture models, ranging from the simpler models (pooled and stratified, closed Petersen estimators) to more complex multi‐strata models (closed Darroch and open Hilborn). The Akaike Information Criterion, corrected (AICc) was used as a model comparison statistic. Results Our best estimate of whale abundance in northern Southeast Alaska in 2000 is 961 whales [95% confidence interval (657, 1076)]. This estimate comes from the Hilborn open, multi‐strata approach with constant migration over time, time‐dependent capture probabilities by area, and a fixed survival rate of 0.98. The simpler models were problematic owing to several aspects of whale behaviour, including that (1) the whales did not mix randomly throughout the study area, (2) some whales emigrated temporarily outside the study area and were not available for capture, and (3) whales were not equally identifiable because they did not behave in the same way when they showed their flukes upon diving. This led to heterogeneity in capture probability and a bias in the estimates. The more complex models stratified by area, and using migration movements among areas, compensated for some of these issues when estimating population size. Main conclusions We believe that the Hilborn open, multi‐strata model produced the best estimate because: (1) it incorporated the best information about survival, (2) it used detailed information about the various release groups, (3) the analysis provided an integrated environment in which parameters such as migration and capture probabilities are shared, (4) the three strata encompassed a large portion of the areas used by whales, and (5) the Hilborn model selected was superior in terms of model selection criteria and biological realism. These data provide valuable insights into the numbers and movements of humpback whales in three areas of Southeast Alaska.     

THE EVOLUTIONARY HISTORY OF CETACEAN BRAIN AND BODY SIZE

Cetaceans rival primates in brain size relative to body size and include species with the largest brains and biggest bodies to have ever evolved. Cetaceans are remarkably diverse, varying in both phenotypes by several orders of magnitude, with notable differences between the two extant suborders, Mysticeti and Odontoceti. We analyzed the evolutionary history of brain and body mass, and relative brain size measured by the encephalization quotient (EQ), using a data set of extinct and extant taxa to capture temporal variation in the mode and direction of evolution. Our results suggest that cetacean brain and body mass evolved under strong directional trends to increase through time, but decreases in EQ were widespread. Mysticetes have significantly lower EQs than odontocetes due to a shift in brain:body allometry following the divergence of the suborders, caused by rapid increases in body mass in Mysticeti and a period of body mass reduction in Odontoceti. The pattern in Cetacea contrasts with that in primates, which experienced strong trends to increase brain mass and relative brain size, but not body mass. We discuss what these analyses reveal about the convergent evolution of large brains, and highlight that until recently the most encephalized mammals were odontocetes, not primates.     

Vocal activity of tropical dolphins is inhibited by the presence of killer whales,Orcinus orca

Research has suggested killer whale (Orcinus orca) predation may affect cetacean vocal behavior; however, few data exist to test this hypothesis. Data collected during 40,976 km of visual and acoustic shipboard surveys in the tropical Pacific Ocean, including 1,232 detections of 13 species, were examined to determine if changes in dolphin vocal activity could be attributed to the presence of killer whales. Generalized linear models and Random Forest analyses were used to test the hypothesis that dolphin vocal activity was related to the distance and time to the nearest killer whale sighting. Both results show that dolphin vocalizations were inversely correlated with the temporal proximity of killer whales (P < 0.05). Despite the relative rarity of killer whales in the tropics, they appear to influence vocal behavior of nearby dolphin schools. This disruption in communication may not significantly impact interactions necessary for survival in tropical waters where killer whale density is low. However, in temperate climates, where increased productivity supports a greater abundance of killer whales, this interruption in communication may have a greater impact. The lower incidence of whistling dolphins in temperate waters may be related to the greater abundance of killer whales in these areas.     

Implication of life history strategies for prenatal investment in cetaceans

Prenatal investment directly determines the size at birth and fetus growth rate, which affects neonatal survival and growth and potentially affects maternal fitness. This study explored the associated prenatal life history traits of cetaceans. Using multivariate analysis and ANCOVA, baleen whales and toothed cetaceans had distinct energy patterns, with two exceptions including beaked whales and eusocial cetaceans. Baleen whales are characterized by fast prenatal growth, which suggests high prenatal energetics, and utilize the capital breeder tactic. Toothed cetaceans, except for beaked whales, utilize income breeder energetics, which yields relatively slow prenatal growth. However, eusocial cetaceans have especially slow prenatal growth, suggesting very low prenatal energetic effort with social compensation. Although beaked whales are behaviorally income breeders, both discriminant analysis and ANCOVA showed that they are energetically similar to baleen whales, utilizing capital energetics. ANCOVA further revealed that beaked whales have comparatively large calf size, suggesting high prenatal investment. Because all cetaceans wean their calves at comparable size, high prenatal investment may further suggest reduced cost of lactation, which may be behaviorally and energetically adaptive to their specific deep‐dive‐feeding niche.     

Evidence that ship noise increases stress in right whales

Baleen whales (Mysticeti) communicate using low-frequency acoustic signals. These long-wavelength sounds can be detected over hundreds of kilometres, potentially allowing contact over large distances. Low-frequency noise from large ships (20-200 Hz) overlaps acoustic signals used by baleen whales, and increased levels of underwater noise have been documented in areas with high shipping traffic. Reported responses of whales to increased noise include: habitat displacement, behavioural changes and alterations in the intensity, frequency and intervals of calls. However, it has been unclear whether exposure to noise results in physiological responses that may lead to significant consequences for individuals or populations. Here, we show that reduced ship traffic in the Bay of Fundy, Canada, following the events of 11 September 2001, resulted in a 6 dB decrease in underwater noise with a significant reduction below 150 Hz. This noise reduction was associated with decreased baseline levels of stress-related faecal hormone metabolites (glucocorticoids) in North Atlantic right whales (Eubalaena glacialis). This is the first evidence that exposure to low-frequency ship noise may be associated with chronic stress in whales, and has implications for all baleen whales in heavy ship traffic areas, and for recovery of this endangered right whale population.