The Relationship between Vessel Traffic and Noise Levels Received by Killer Whales (Orcinus orca)

Whale watching has become increasingly popular as an ecotourism activity around the globe and is beneficial for environmental education and local economies. Southern Resident killer whales (Orcinus orca) comprise an endangered population that is frequently observed by a large whale watching fleet in the inland waters of Washington state and British Columbia. One of the factors identified as a risk to recovery for the population is the effect of vessels and associated noise. An examination of the effects of vessels and associated noise on whale behavior utilized novel equipment to address limitations of previous studies. Digital acoustic recording tags (DTAGs) measured the noise levels the tagged whales received while laser positioning systems allowed collection of geo-referenced data for tagged whales and all vessels within 1000 m of the tagged whale. The objective of the current study was to compare vessel data and DTAG recordings to relate vessel traffic to the ambient noise received by tagged whales. Two analyses were conducted, one including all recording intervals, and one that excluded intervals when only the research vessel was present. For all data, significant predictors of noise levels were length (inverse relationship), number of propellers, and vessel speed, but only 15% of the variation in noise was explained by this model. When research-vessel-only intervals were excluded, vessel speed was the only significant predictor of noise levels, and explained 42% of the variation. Simple linear regressions (ignoring covariates) found that average vessel speed and number of propellers were the only significant correlates with noise levels. We conclude that vessel speed is the most important predictor of noise levels received by whales in this study. Thus, measures that reduce vessel speed in the vicinity of killer whales would reduce noise exposure in this population.     

Killer whale (Orcinus orca) reproduction at Sea World

Sea World has maintained killer whales (Orcinus orca) since 1965. The total killer whale inventory (1965–1993) has included 39 whales (25 females, 14 males); 28 were wild-caught and 11 captive-born, including one second-generation calf. As of September, 1993, there were 19 whales in the breeding program. Ten of these whales (53%) were captive-born, either at Sea World or other facilities in North America. The live wild-caught whales ranged in estimated age from 12–27 years (x? ± sd = 17.6 ± 4.2 years). The captive-born whales ranged in age from <1 to 8 years. In the Sea World breeding program (through September, 1993), there have been nine live births and one stillbirth, with eight calves part of the current inventory. Births occurred from July to February. Calving intervals ranged from 32–58 months. Female age at birth of first calves ranged from 8 years to an estimated 17 years (x? ± sd = 12.7 ± 3.0 years). Gestation, based on conception estimates from serum progesterone analysis, averaged 17 months (x? ± sd = 517 ± 20 days), but successful pregnancies with viable calves occurred from 15–18 months (468–539 days). Females, in the presence and absence of males, were polyestrus with periods of cycling interspersed with individually variable noncycling (presumed anestrous) periods ranging from 3–16 months. Mean serum progesterone levels (±se) were as follows: noncycling periods = 121 ± 20 pg/ml; peak elevations during nonconceptive ovulatory (estrous) cycles = 3,962 ± 2,280 pg/ml; first pregnancies = 14,592 ± 3,854 pg/ml; second pregnancies = 8,389 ± 395 pg/ml; and third pregnancy = 8,180 ± 4,556. © 1995 Wiley-Liss, Inc.     

Killer whale (Orcinus orca) predation in a multi-prey system

Predation can regulate prey numbers but predator behaviour in multiple-prey systems can complicate understanding of control mechanisms. We investigate killer whale (Orcinus orca) predation in an ocean system where multiple marine mammal prey coexist. Using stochastic models with Monte-Carlo simulations, we test the most likely outcome of predator selection and compare scenarios where killer whales: (1) focus predation on larger prey which presumably offer more energy per effort, (2) generalize by feeding on prey as encountered during searches, or (3) follow a mixed foraging strategy based on a combination of encounter rate and prey size selection. We test alternative relationships within the Hudson Bay geographic region, where evidence suggests killer whales seasonally concentrate feeding activities on the large-bodied bowhead whale (Balaena mysticetus). However, model results indicate that killer whales do not show strong prey specialization and instead alternatively feed on narwhal (Monodon monoceros) and beluga (Delphinapterus leucas) whales early and late in the ice-free season. Evidence does support the conjecture that during the peak of the open water season, killer whale predation can differ regionally and feeding techniques can focus on bowhead whale prey. The mixed foraging strategy used by killer whales includes seasonal predator specialization and has management and conservation significance since killer whale predation may not be constrained by a regulatory functional response.     

Temporal and Contextual Patterns of Killer Whale (Orcinus orca) Call Type Production

Fish-eating killer whales Orcinus orca in the northeastern Pacific live in highly stable matrifocal social groups called pods. Each pod produces a repertoire of seven or more stereotyped call types. We compared the relative production of call types of free-ranging killer whale pods over time and between social contexts. The relative production of call types by each pod during directional travel was distinct over a 27-yr period; however, both temporal stability and pod distinctiveness were strongly influenced by a subset of dominant call types within the repertoire of each pod. Some call types within the repertoires contain biphonation (two overlapping independently modulated tones) and have a higher estimated active space than call types containing just one tone. In multi-pod aggregations the relative production of the dominant call types of each pod decreased and the relative production of a subset of call types that are rarely recorded from single-pod groupings increased. The majority of these contained biphonation. The data suggest a distinction between a subset of dominant call types that may function to identify the pod and a subset of less common call types including several call types containing biphonation that are more commonly produced during inter-pod affiliations.     

Killer whales (Orcinus orca) feeding on lumpfish (Cyclopterus lumpus) in northern Norway

Killer whales (Orcinus orca) in Norwegian waters have long been known to rely on Atlantic herring (Clupea harengus) as a main prey resource. However, research almost exclusively conducted at seasonal herring grounds may have biased studies away from detecting other potentially significant prey species. Since 2013, dedicated research efforts have focused on monitoring killer whale occurrence and foraging ecology throughout the year in northern Norway. This study presents results on site-fidelity of photographically identified individuals, predation records and behavioral patterns from five spring seasons (March–April) in 2014–2018 in Andfjord, northern Norway. A minimum number of 75 adult and subadult killer whales (out of a catalog of 971 individuals) returned seasonally to the study area for foraging and residency for up to six weeks. Lumpfish (or lumpsucker, Cyclopterus lumpus) was the only type of prey identified (based on molecular or visual identification) on 22 predation events from 2016 (n = 4), 2017 (n = 2) and 2018 (n = 16). Spatial group cohesion observed when foraging was a potential adaptation for efficiently hunting this prey species. These whales were also encountered at herring wintering grounds the same years, but with different group sizes. Such behavioral adaptations suggested intraannual switching between prey resources and foraging strategies.     

Inferred Paternity and Male Reproductive Success in a Killer Whale (Orcinus orca) Population

We used data from 78 individuals at 26 microsatellite loci to infer parental and sibling relationships within a community of fish-eating ("resident") eastern North Pacific killer whales (Orcinus orca). Paternity analysis involving 15 mother/calf pairs and 8 potential fathers and whole-pedigree analysis of the entire sample produced consistent results. The variance in male reproductive success was greater than expected by chance and similar to that of other aquatic mammals. Although the number of confirmed paternities was small, reproductive success appeared to increase with male age and size. We found no evidence that males from outside this small population sired any of the sampled individuals. In contrast to previous results in a different population, many offspring were the result of matings within the same "pod" (long-term social group). Despite this pattern of breeding within social groups, we found no evidence of offspring produced by matings between close relatives, and the average internal relatedness of individuals was significantly less than expected if mating were random. The population's estimated effective size was <30 or about 1/3 of the current census size. Patterns of allele frequency variation were consistent with a population bottleneck.     

Captive killer whale (Orcinus orca) survival

Killer whales (Orcinus orca) were first placed into captivity in 1961 and are now found in theme parks around the world. Despite successful breeding of captive killer whales since 1985 there is growing concern for their welfare in captivity, which often includes claims of poor survival. We employed Kaplan‐Meier and Cox Proportional hazards models and annual survival rate analyses on 201 captive killer whales to discern how sex, facility (U.S. vs. foreign), captive‐born vs. wild‐captured, pre‐ vs. post‐1 January 1985, and animal age upon entering captivity affect survival. Overall median survival estimate was 6.1 yr, with no difference between male and female survival. Killer whales in U.S. facilities (12.0 yr) demonstrated a significantly higher median survival than those in foreign facilities (4.4 yr), as did whales entering captivity post‐1 January 1985 (11.8 yr) vs. those entering prior to 1 January 1985 (3.9 yr). Median survival for captive‐born (14.1 yr) was significantly higher than wild‐captured killer whales (5.5 yr), though the two failed to differ among the post‐1 January 1985 cohort. Facility location and pre‐ vs. post‐1 January 1985 were predictors of the hazard rate. Survival of captive killer whale cohorts has generally improved through time, although survival to age milestones are poor when compared to wild killer whales.     

Killer whales (Orcinus orca) hunting for walruses (Odobenus rosmarus divergens) near Retkyn Spit, Chukotka

Group hunting by killer whales for walruses was observed in August 18, 2008, in the littoral area (3 km from the haulout of walruses, Retkyn Spit, Chukotka). The group of killer whales consisted of seven adults (one adult male did not participate in attacks) and two calves. Based on prey type, these killer whales were mammal-eating. The total duration of their hunt activity was not less than 95 min. The hunt consisted of three phases. The first phase was an attack on the group of walruses and choice of individual prey; the second phase was attacks on the chosen walrus; and the third (final) phase was a decrease in activity of killer whales and leaving group with walrus from sea shore. The main behavioral patterns of killer whales during the hunt were discerned. Two killer whales tried to kill walruses by chasing them and jumping out of the water on the shore. The video analysis of the ??attack phase?? showed that killer whales made 55 attacks on the walrus during 17.3 min. On average, each killer whale attacked the walrus seven times. The attack tactics of killer whales, the number of movements, and the location of killer whales (adults and calves) relative to each other and to the walrus were described. Well coordination of their movements and group actions was observed.     

Social interaction analysis in captive orcas (Orcinus orca)

The management of socially complex species in captivity is challenging. Research on their social behavior improves our understanding of interactions in captive animals and captive‐group management. We conducted a detailed analysis of social relationships shown by the orcas kept at Loro Parque zoo and their tendency to reconcile after aggressive episodes. Affiliative interactions were the most frequent social activities compared to agonistic or sexual interactions. Within affiliative behaviors, we documented the pattern “gentle tongue bite”, where an animal touches the other's tongue with his teeth but does not bite it. Affiliative interactions between a specific pair of orcas occurred significantly more often than expected by chance, and together with low levels of agonistic interactions, indicated particular affinity between some individuals. The most frequently observed low‐level agonistic relationship was that of the two older males (Tekoa–Keto); however, they also showed frequent sexual and affiliative interactions. Sexual‐like behaviors (pursuit, mount, and penis between males) were found in both sexes. Finally, the observed corrected conciliatory tendency (31.57%) was within the range described for other primate and cetacean species. This study provides a systematic way to assess social interactions as well as conflict management strategies in cetaceans housed in zoos and zoo‐like facilities and may help to improve animal welfare and management of animals in controlled environments.     

The seasonal occurrence and behaviour of Killer whales Orcinus orca, at Marion Island

The paper describes the occurrence of Killer whales at Marion Island (Prince Edward group) in the south Indian Ocean from August 1973 to November 1976. They occur seasonally, being most numerous from October to December. Their occurrence is synchronized with the seasonal haul out of Southern elephant seals, but the seasonality of King, Rockhopper and Macaroni penguins is also likely to influence their occurrence. The largest herds occur in October, the month during which mean group size is also largest. Sex and age composition are given, adult males being significantly more numerous than adult females, while 36–3 % of the latter had calves. Hunting activity appears to be greatest between 15.00 and 17.00 hrs, and most Killer whales were seen within 100 m of the shore. Aspects of hunting, attacking, feeding and resting behaviour are discussed. The body measurements of a young male found on a beach are given.     

Nursing parameters in captive killer whales (Orcinus orca)

We examined nursing behaviors for a population of captive‐born killer whales (four females, three males) at SeaWorld parks from birth until 90 days of age. Nursing parameters examined included cumulatives of suckles per day, bouts per day, and suckle duration (seconds) per day. Daily cumulatives of all nursing parameters peaked within the first 2 days after birth then decreased through time. For the ages from birth until 42 days, data were converted using log_e‐log_e transformations to allow linear regression modeling. Since these parameters were characterized by autocorrelation, bootstrapping was used to obtain parameter estimates for comparisons between sexes and cow parity. Both males and females, as well as calves born to primiparous and multiparous cows, exhibited similar nursing patterns. However, there were statistically significant differences (α < 0.05) between the regression equations among most of the nursing parameters examined. Cumulative frequencies and amounts from birth through 42 days of age for all nursing parameters were examined. Means were statistically similar (α > 0.05) between genders (means[sd] for males and females, respectively; suckles 3,772.7[412.4] and 3,276.3[1,226.5]; bouts 1,238.3[189.0] and 1,103.3[96.4]; suckle duration [seconds] 28,990.7[5,861.9] and 29,233.0[5,255.0]) and cow parity (means[sd] for primiparous and multiparous, respectively; suckles 4,459.0[606.7] and 3,101.0[753.8]; bouts 1,240.0[243.3] and 1,129.6[116.2]; suckle duration [seconds] 32,415.0[5,212.8] and 27,814.8[4854.5]). Equal amounts of nursing occurred from both left and right mammary glands for the 42‐day time period (means[sd] [seconds] for left and right, respectively; 13,800.4[2,787.0] and 15,328.7[2,471.0]; P = 0.30). Zoo Biol 18:373–384, 1999. © 1999 Wiley‐Liss, Inc.     

Killer whales (Orcinus orca) in the Canadian Arctic: Distribution,prey items,group sizes,and seasonality

Killer whales (Orcinus orca) have a global distribution, but many high‐latitude populations are not well studied. We provide a comprehensive review of the history and ecology of killer whales in the Canadian Arctic, for which there has previously been little information. We compiled a database of 450 sightings spanning over 15 decades (1850–2008) to document the historical occurrence, distribution, feeding ecology, and seasonality of killer whales observed throughout the region. Sighting reports per decade increased substantially since 1850 and were most frequent in the eastern Canadian Arctic. The mean reported group size was 8.3 (median = 4, range 1–100), but size varied significantly among regions and observed prey types. Observations of predation events indicate that Canadian Arctic killer whales prey upon other marine mammals. Monodontids were the most frequently observed prey items, followed by bowhead whales (Balaena mysticetus), phocids, and groups of mixed mammal prey. No killer whale sightings occurred during winter, with sightings gradually increasing from early spring to a peak in summer, after which sightings gradually decreased. Our results suggest that killer whales are established, at least seasonally, throughout the Canadian Arctic, and we discuss potential ecological implications of increased presence with declining sea ice extent and duration.     

Killer whale (Orcinus orca) population dynamics in response to a period of rapid ecosystem change in the eastern North Atlantic

This study investigates survival and abundance of killer whales (Orcinus orca) in Norway in 1988–2019 using capture–recapture models of photo‐identification data. We merged two datasets collected in a restricted fjord system in 1988–2008 (Period 1) with a third, collected after their preferred herring prey shifted its wintering grounds to more exposed coastal waters in 2012–2019 (Period 2), and investigated any differences between these two periods. The resulting dataset, spanning 32 years, comprised 3284 captures of 1236 whales, including 148 individuals seen in both periods. The best‐supported models of survival included the effects of sex and time period, and the presence of transients (whales seen only once). Period 2 had a much larger percentage of transients compared to Period 1 (mean = 30% vs. 5%) and the identification of two groups of whales with different residency patterns revealed heterogeneity in recapture probabilities. This caused estimates of survival rates to be biased downward (females: 0.955 ± 0.027 SE, males: 0.864 ± 0.038 SE) compared to Period 1 (females: 0.998 ± 0.002 SE, males: 0.985 ± 0.009 SE). Accounting for this heterogeneity resulted in estimates of apparent survival close to unity for regularly seen whales in Period 2. A robust design model for Period 2 further supported random temporary emigration at an estimated annual probability of 0.148 (± 0.095 SE). This same model estimated a peak in annual abundance in 2015 at 1061 individuals (95% CI 999–1127), compared to a maximum of 731 (95% CI 505–1059) previously estimated in Period 1, and dropped to 513 (95% CI 488–540) in 2018. Our results indicate variations in the proportion of killer whales present of an undefined population (or populations) in a larger geographical region. Killer whales have adjusted their distribution to shifts in key prey resources, indicating potential to adapt to rapidly changing marine ecosystems.     

Observations of killer whales (Orcinus orca) in the fjords of Chilean Patagonia

Killer whales occur in Chilean waters, but their seasonality, diets, and overall distribution are poorly known. Here, we present data on group composition, site fidelity, and prey species of individual killer whales recorded in 63 sightings between 2004 and 2012 in the Chilean Patagonian fjords. Group sizes were small (mean = 5, SD = 2.5 for calf groups; mean = 3, SD = 1.5 for non-calf groups), and occurrence was significantly lower in summer months. Photographs enabled identification of 55 individuals from natural markings, and all resembled Southern Ocean type A killer whales. The species was transient in the area; the average presence was 1.7 days with 60 % of individuals seen only once. Occupancy was 3–44 days, and low levels of site fidelity were recorded (64 % of individuals were seen in only 1 year). Group composition at short time scales (3 months) remained stable, but we detected changes at longer time scales. Prey included fish, otariids, and seabirds. Twelve individual killer whales showed a broad dietary spectrum: 3 ate otariids and fish, 2 ate birds and otariids, and 7 ate otariids, birds, and possibly fish. Further research is needed to increase basic biological knowledge of these killer whales and to determine the relationship with type A killer whales from the Southern Ocean.     

Salmonella Newport omphaloarteritis in a stranded killer whale (Orcinus orca) neonate

Salmonella enterica serovar Newport (Salmonella Newport) was isolated from multiple tissues in a neonate killer whale (Orcinus orca) that stranded dead in 2005 along the central coast of California, USA. Necrotizing omphaloarteritis and omphalophlebitis was observed on histologic examination suggesting umbilical infection was the route of entry. Genetic analysis of skin samples indicated that the neonate had an offshore haplotype. Salmonellosis has rarely been identified in free-ranging marine mammals and the significance of Salmonella Newport infection to the health of free-ranging killer whales is currently unknown.