THREE MASS STRANDINGS OF SPERM WHALES (PHYSETER MACROCEPHALUS) IN SOUTHERN AUSTRALIAN WATERS

One hundred and fifteen sperm whales (97 female, 15 male, 3 unknown sex) were involved in three mass stranding events during the month of February 1998 along the west and northwest coastlines of Tasmania, Australia. Sixty-six of these whales stranded at Ocean Beach, Strahan; 35 at Greens Beach, Marrawah; and 11 at Black River Beach, Stanley. The remaining whales stranded singly along the coastline. Three mass strandings of this species in such close temporal proximity have not been reported in this area before, and this is the first time that data have been comprehensively collected from complete or near-complete groups of sperm whales from Tasmanian waters. Adult females dominated the three stranding groups. Total lengths ranged from 417 to 1,200 cm and ages ranged from 0.75 to 64 yr. Four females were lactating and four fetuses were found amongst the groups. Stomach contents were dominated by pelagic cephalopods.     

OPEN-BOAT WHALING ON THE STRAITS OF GIBRALTAR GROUND AND ADJACENT WATERS

Logbooks ( n = 317) from whaling expeditions made in the North Atlantic during the 19th century were examined to investigate activity in the Gibraltar Straits grounds. At least forty expeditions of whaling vessels from European and American ports visited the area. In all cases the main target was the sperm whale, but pilot whales, dolphins, sea turtles, and even a blue whale were also taken. Whaling effort concentrated on the Atlantic side of the Straits; only two expeditions ventured into the Mediterranean Sea, obtaining negligible catches. The whaling season extended during spring and summer and peaked in June–July. This seasonality appeared not to be governed by changes in whale density but by the trade winds necessary to sail southward or westward to cross the Atlantic. Searching effort continued while trying out, but the rate of sighting cetaceans was about half that of searching periods. However, the rate of sighting or capturing a sperm whale remained unchanged during processing, probably because the gregarious habits of the species produced clumping of catches. For every whale secured, 1.31 whales were struck. After correcting for struck but lost whales and for "gammed" vessels, the minimum number of removals of sperm whales during 1862–1889 is estimated at 237.     

BLUE WHALE VISUAL AND ACOUSTIC ENCOUNTER RATES IN THE SOUTHERN CALIFORNIA BIGHT

The relationship between blue whale ( Balaenoptera musculus ) visual and acoustic encounter rates was quantitatively evaluated using hourly counts of detected whales during shipboard surveys off southern California. Encounter rates were estimated using temporal, geographic, and weather variables within a generalized additive model framework. Visual encounters (2.06 animals/h, CV = 0.10) varied with subregion, Julian day, time of day, and year. Acoustic encounters of whales producing pulsed A and tonal B call sequences (song; 0.65 animals/h, CV = 0.06) varied by Julian day, survey mode (transit or stationary), and subregion, and encounters of whales producing downswept (D) calls (0.41 animals/h, CV = 0.09) varied by Julian day and the number of animals seen. Inclusion of Julian day in all models reflects the seasonal occurrence of blue whales off southern California; however, the seasonal peak in visual encounters and acoustic encounters of D calling whales (July–August) was offset from the peak in acoustic encounters of singing whales (August–September). The relationship between visual and acoustic encounter rates varied regionally, with significant differences in several northern regions. The number of whales heard D calling was positively related to the number of animals seen, whereas the number of singing whales was not related to visual encounter rate.     

HAS THE AGE AT TRANSITION OF SOUTHERN HEMISPHERE MINKE WHALES DECLINED OVER RECENT DECADES?

The earplugs of several baleen whale stocks exhibit seasonal growth layers which have been shown for some species to indicate the total age of the animals. A transition from early, irregular layers, to later, more regular layers can be seen in these earplugs, and this is thought to indicate the age at maturity of the whale. The earplugs of Southern Hemisphere minke whales are relatively difficult to read, particularly for the age at transition, and it has been suggested that these readings reflect no more than random allocations by the reader, rather than any real effect. Plots of average transition phase against year of birth (cohort) show a decline in the average age at transition. However, certain factors can result in a downward bias in this trend, particularly when only a short time-series is available for analysis, as was the case when this trend was first estimated some 15 yr ago. Data collected over 25 yr are now available and are reanalyzed here. A plot of mean age at transition against year of sampling for animals of similar age shows a decline, as does the conventional plot against cohort, suggesting that the decline is real. A model that simulates random allocation of the transition phase by earplug readers yields predictions that show systematic deviations from the data. In contrast, a second model that allows for a real trend in the average age at transition and that takes account of two potentially biasing effects (termed truncation and the fringe effect) fits the data well. A tendency is evident for readers to recognize a transition phase in a greater proportion of the earplugs that they read as they gain experience over time. This is taken into account in the model. This model shows a decline in the average age at transition from roughly 11 for the cohorts of the 1950s to roughly 7 for those of the 1970s. These results suggest that minke whale transition-phase readings are related to a real signal in the data and are not simply an artefact, and further that there has been a real decline in the age to which this signal corresponds.     

North Atlantic minke whale (Balaenoptera acutorostrata) feeding habits and migrations evaluated by stable isotope analysis of baleen

Isotopic analyses of the incrementally growing baleen in Mysticeti have been used to learn about their feeding and movement patterns. Using methods previously applied to Pacific minke whales, stable δ¹⁵N and δ¹³C isotope values were measured along the baleen plates of male and female minke whales from two locations in the Northeast Atlantic. The sample sizes used in this study are comparable to those previously used in the literature, and, although limited in size, the evidence suggests differences in isotopic signatures between whales caught at different locations. Both the δ¹⁵N and δ¹³C data suggest whales at the higher latitude site of Svalbard have a narrower diet than the whales from Lofoten/Vesterålen in Norway. Across all whales, the δ¹⁵N data indicate the whales primarily prey on fish for much of the year, only switching to zooplankton during the spring bloom. The δ¹³C data fail to confirm whether the whales migrate over long distances.     

Photo-identification and satellite telemetry connect southern right whales from South Georgia Island (Islas Georgias del Sur) with multiple feeding and calving grounds in the southwest Atlantic

The sub-Antarctic waters of South Georgia Island (Islas Georgias del Sur, SG/IG) are a regularly visited feeding ground for southern right whales (Eubalaena australis, SRW) in the southwest Atlantic. Satellite telemetry and photo-identification records were compared to better understand the role of SG/IG in the SRW migratory network. We present the first insights from SRW satellite-tracked from the SG/IG feeding ground, habitat use patterns in the Scotia Arc, and movements to Antarctic habitats. Photo-identification comparisons to calving and feeding areas across the South Atlantic and a review of sightings of cetaceans reported from Bird Island (west of SG/IG) since 1979 illuminate long-term habitat use patterns in SG/IG. We present the first recorded migratory movement between SG/IG and multiple countries: Argentina, Uruguay, and Brazil. Photo-identification (1) linked SG/IG to a female SRW with a long-term sighting history in Brazil, and (2) provided the first match between SG/IG and the western Antarctic Peninsula, suggesting the latter could extend the feeding area for southwest Atlantic SRW. Satellite tracking and opportunistic sightings suggest that shelf and coastal waters west of SG/IG represent an important multi-season SRW feeding habitat and add to our overall understanding of habitats and ranges occupied by recovering southwest Atlantic SRW.     

Reproductive parameters of Bering-Chukchi-Beaufort Seas bowhead whales

Data from Bering-Chukchi-Beaufort Seas bowhead whales (Balaena mysticetus), harvested during 1973–2021 by aboriginal subsistence hunters, were used to estimate reproductive parameters: length at sexual maturity (LSM), age at sexual maturity (ASM), pregnancy rate (PR), and calving interval. Sexual maturity (N = 187 females) was determined from the presence/absence of corpora in the ovaries, or a fetus. Using sampling bias-corrected logistic regression, LSM was estimated at 13.5 m, 95% CI [13.0, 13.8]. There was a downward trend in LSM over time, statistically significant with one method but marginal with another. A growth model translated this estimate to an ASM estimate of 23.5 years, 95% CI [20.4, 26.7]. Pregnancy rate was determined from mature females (N = 125), and from a subset limited to certain autumn-caught whales (n = 37) to reduce bias. The PR was estimated at 0.46 globally, 95% CI [0.36, 0.55] and 0.38 for the autumn sample, 95% CI [0.20, 0.51]. Both estimated PRs are consistent with a 3-year calving interval, because the larger estimate includes two cohorts of pregnant whales harvested in spring, and bowhead whale gestation is longer than 12 months. These analyses represent the most conclusive empirical estimates of ASM, LSM, and PR for this bowhead whale stock from the largest available data sets to date.     

Evidence for the functions of surface‐active behaviors in humpback whales (Megaptera novaeangliae)

As part of their social sound repertoire, migrating humpback whales (Megaptera novaeangliae) perform a large variety of surface‐active behaviors, such as breaching and repetitive slapping of the pectoral fins and tail flukes; however, little is known about what factors influence these behaviors and what their functions might be. We investigated the potential functions of surface‐active behaviors in humpback whale groups by examining the social and environmental contexts in which they occurred. Focal observations on 94 different groups of whales were collected in conjunction with continuous acoustic monitoring, and data on the social and environmental context of each group. We propose that breaching may play a role in communication between distant groups as the probability of observing this behavior decreased significantly when the nearest whale group was within 4,000 m compared to beyond 4,000 m. Involvement in group interactions, such as the splitting of a group or a group joining with other whales, was an important factor in predicting the occurrence of pectoral, fluke, and peduncle slapping, and we suggest that they play a role in close‐range or within‐group communication. This study highlights the potentially important and diverse roles of surface‐active behaviors in the communication of migrating humpback whales.