Seasonal distribution, exploitation and present abundance of stocks of large baleen whales (Mysticeti) and sperm whales (Physeter macrocephalus) in Norwegian and adjacent waters

1992 ◽  
Vol 49 (3) ◽  
pp. 341-355 ◽  
Author(s):  
I. Christensen ◽  
T. Haug ◽  
N. Oien
2000 ◽  
Vol 78 (3) ◽  
pp. 407-419 ◽  
Author(s):  
Nathalie Jaquet ◽  
Stephen Dawson ◽  
Elisabeth Slooten

Male sperm whales (Physeter macrocephalus) were the preferred target of the whaling industry between 1950 and 1985, but despite hundreds of thousands of kills, very little is known about their ecology. To partially redress this, we present data on residency, seasonal distribution, and diving behaviour of individually identified sperm whales off Kaikoura, South Island, New Zealand, gathered during 15 field seasons over 8 years. One hundred and thirty-six sperm whales were identified within the study area. A lack of statistically significant differences in the abundance of sperm whales between summer and winter, and among the 15 seasons of fieldwork, suggests an adequate food supply year-round. Significant differences in distribution between summer and winter suggest that off Kaikoura, male sperm whales may change their diet in response to fluctuations in prey biomass. Diving behaviour was also significantly different between summer and winter: sperm whales dived for longer, stayed longer at the surface, and travelled farther between consecutive fluke-ups in summer than in winter. Unlike female sperm whales, males at Kaikoura spent little time at the surface; they spent about 83% of their total time under water. This paper represent the most extensive non-invasive study of male sperm whales and provides new insights into their ecology.


1985 ◽  
Vol 63 (6) ◽  
pp. 1402-1409 ◽  
Author(s):  
Donald F. McAlpine

Size and growth of heart, liver, and kidneys in fin (Balaenoptera physalus), sei (B. borealis), and sperm (Physeter macrocephalus) whales taken commercially off Iceland during the 1980 season are compared and examined relative to organ weights for terrestrial mammals. In agreement with the work of previous investigators, the sperm whale is shown to have a relatively smaller heart. However, contrary to previous analysis, fin and sei whales are shown to have relative heart sizes not radically different from those of terrestrial mammals. It is suggested that the differences in relative heart size between the baleen and toothed whales are a reflection of the greater swimming speeds that the baleen whales are capable of attaining. This analysis confirms that marine cetaceans have relatively much larger livers than terrestrial mammals and that they also appear to have relatively larger kidneys. The results presented here, however, show fin, sei, and sperm whales to have relative kidney sizes less than half as great as those given in previous analyses. Growth gradients in the three organs show a distinct pattern of divergence between sperm (Odontocete) and fin and sei (Mysticete) whales.


2021 ◽  
Author(s):  
Stefanie P. Glaeser ◽  
Liliana M. R. Silva ◽  
Rui Prieto ◽  
Mónica A. Silva ◽  
Angel Franco ◽  
...  

AbstractLarge baleen and toothed whales play crucial ecological roles in oceans; nonetheless, very little is known about their intestinal microbiomes. Based on striking differences in natural history and thus in feeding behaviours, it can be expected that intestinal microbiomes of large baleen whales and toothed whales are different. To test this hypothesis, the phylogenetic composition of faecal microbiomes was investigated by a 16S rRNA gene amplicon sequence–based approach for Bacteria and Archaea. Faecal samples from free-ranging large whales collected off the Azores Archipelago (Portugal) were used, comprising 13 individual baleen whales (one sei, two blue and ten fin whales) and four sperm whales. The phylogenetic composition of the Bacteria faecal microbiomes of baleen and toothed whales showed no significant differences at the phylum level. However, significant differences were detected at the family and genus levels. Most abundant phyla were Firmicutes, Bacteroidetes, Proteobacteria, Tenericutes and Spirochaeta. Few highly abundant bacterial genera were identified as key taxa with a high contribution to differences among baleen and toothed whales microbiomes. Only few archaeal sequences were detected, primarily Methanomassiliicoccales representing potential methanogenic Archaea. This is the first study that directly compares the faecal bacterial and archaeal microbiomes of free-ranging baleen and toothed whales which represent the two parvorders of Cetacea which members are fully aquatic large mammals which were evolutionary split millions of years ago.


2021 ◽  
Vol 9 (4) ◽  
pp. 444
Author(s):  
Charlotte Curé ◽  
Saana Isojunno ◽  
Marije L. Siemensma ◽  
Paul J. Wensveen ◽  
Célia Buisson ◽  
...  

Controlled exposure experiments (CEEs) have demonstrated that naval pulsed active sonar (PAS) can induce costly behavioral responses in cetaceans similar to antipredator responses. New generation continuous active sonars (CAS) emit lower amplitude levels but more continuous signals. We conducted CEEs with PAS, CAS and no-sonar control on free-ranging sperm whales in Norway. Two panels blind to experimental conditions concurrently inspected acoustic-and-movement-tag data and visual observations of tagged whales and used an established severity scale (0–9) to assign scores to putative responses. Only half of the exposures elicited a response, indicating overall low responsiveness in sperm whales. Responding whales (10 of 12) showed more, and more severe responses to sonar compared to no-sonar. Moreover, the probability of response increased when whales were previously exposed to presence of predatory and/or competing killer or long-finned pilot whales. Various behavioral change types occurred over a broad range of severities (1–6) during CAS and PAS. When combining all behavioral types, the proportion of responses to CAS was significantly higher than no-sonar but not different from PAS. Responses potentially impacting vital rates i.e., with severity ≥4, were initiated at received cumulative sound exposure levels (dB re 1 μPa2 s) of 137–177 during CAS and 143–181 during PAS.


1988 ◽  
Vol 45 (10) ◽  
pp. 1736-1743 ◽  
Author(s):  
Julia Mullins ◽  
Hal Whitehead ◽  
Linda S. Weilgart

During June 1986, two male sperm whales, Physeter macrocephalus, on the Scotian Shelf were tracked by listening for their clicks with a directional hydrophone for periods of 12.5 and 7 h, respectively. Each whale travelled along the edge of the shelf at about 2 kn (3.6 km/h), and one whale, on two occasions at least, dived to the ocean floor. After about 30 min underwater, the whales spent approximately 9 min at the surface breathing. When the whales were visible at the surface, they were silent, except on one occasion when "slow clicking" (mean interclick interval of 4.6 s) was heard from Whale 2. While underwater, most of the sound production consisted of "usual clicks" (mean interclick interval 0.96 and 0.69 s for the two whales) interrupted by frequent short silences (mean durations 21.06 and 27.82 s) and occasional "creaks" (with interclick intervals less than 0.2 s) and "slow clicks." No "codas" (stereotyped patterns of clicks) were heard from these two single whales. These results are consistent with the hypotheses that "usual clicks" and "creaks" are used for echolocation and "codas" for communication.


1993 ◽  
Vol 71 (10) ◽  
pp. 1991-1996 ◽  
Author(s):  
Sean C. Smith ◽  
Hal Whitehead

The feeding success of sperm whales off the Galápagos Islands, Ecuador, was examined over 5 study years; 1985, 1987, 1988, 1989, and 1991. A total of 160 days were spent following sperm whales at sea. The defaecation rates of sperm whales were used as an indication of feeding success. The recorded acoustic click rates of sperm whales were used as an indication of aggregative and foraging behaviour. Significant variation in feeding success occurred temporally over periods of days, months, and years. Feeding success also varied spatially with geographic area. Feeding success was inversely related to sea surface temperature (SST). The foraging and associative behaviour of sperm whales also varied with feeding success, SST, and by year. Variations in the feeding success and behaviour of Galápagos sperm whales can likely be attributed to changing oceanographic conditions in the waters surrounding the Galápagos archipelago.


1998 ◽  
Vol 76 (5) ◽  
pp. 886-896 ◽  
Author(s):  
Andrew W Trites ◽  
Daniel Pauly

Generalized survival models were applied to growth curves published for 17 species of cetaceans (5 mysticetes, 12 odontocetes) and 13 species of pinnipeds (1 odobenid, 4 otariids, 8 phocids). The mean mass of all individuals in the population was calculated and plotted against the maximum body length reported for each species. The data showed strong linearity (on logarithmic scales), with three distinct clusters of points corresponding to the mysticetes (baleen whales), odontocetes (toothed whales), and pinnipeds (seals, sea lions, and walruses). Exceptions to this pattern were the sperm whales, which appeared to be more closely related to the mysticetes than to the odontocetes. Regression equations were applied to the maximum lengths reported for 76 species of marine mammals without published growth curves. Estimates of mean body mass were thus derived for 106 living species of marine mammals.


2020 ◽  
Vol 11 ◽  
Author(s):  
Deanna Leonard ◽  
Nils Øien

A ship-based mosaic survey of Northeast Atlantic cetaceans was conducted over a 5-year period between 2014–2018. The area surveyed extends from the North Sea in the south (southern boundary at 53oN), to the ice edge of the Barents Sea and the Greenland Sea. Survey vessels were equipped with 2 independent observer platforms that detected whales in passing mode and applied tracking procedures for the target species, common minke whales (Balaenoptera acutorostrata acutorostrata). Here we present abundance estimates for all non-target species for which there were sufficient sightings. We estimate the abundance of fin whales (Balaenoptera physalus) to be 11,387 (CV=0.17, 95% CI: 8,072–16,063), of humpback whales (Megaptera novaeangliae) to be 10,708 (CV=0.38, 95% CI: 4,906–23,370), of sperm whales (Physeter macrocephalus) to be 5,704 (CV=0.26, 95% CI: 3,374–9,643), of killer whales (Orcinus orca) to be 15,056 (CV=0.29, 95% CI: 8,423–26,914), of harbour porpoises (Phocoena phocoena) to be 255,929 (CV=0.20, 95% CI: 172,742–379,175), dolphins of genus Lagenorhynchus to be 192,767 (CV=0.25, 95% CI: 114,033–325,863), and finally of northern bottlenose whales (Hyperoodon ampullatus) to be 7,800 (CV=0.28, 95% CI: 4,373–13,913). Additionally, our survey effort in the Norwegian Sea in 2015 contributed to the 6th North Atlantic Sightings Survey (NASS) and the survey was extended into the waters north and east of Iceland around Jan Mayen island. This NASS extension, along with our Norwegian Sea survey in 2015, was used to estimate the abundance of fin whales, humpback whales, and sperm whales. All estimates presented used mark-recapture distance sampling techniques and were thus corrected for perception bias. Our estimates do not account for additional variance due to distributional shifts between years or biases due to availability or responsive movement.


PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0244204
Author(s):  
Hayao Kobayashi ◽  
Hal Whitehead ◽  
Masao Amano

Little is known about the social structure of male sperm whales (Physeter macrocephalus) after they leave their natal units. While previous studies found no evidence for preferred associations among males, the observation of mass-strandings consisting exclusively of males, suggest that they have strong social bonds. To investigate the social associations among male sperm whales, we used half weight index of association, permutation tests and standardized lagged association rate models on a large photo-identification database collected between 2006 and 2017 in Nemuro Strait, Japan. Our results suggest that while male sperm whales are not as social as females, they do form long term associations, have preferred companionship, and forage in social proximity to each other. The best-fitting model to the standardized lagged association rate showed that associations among males last for at least 2.7 years and as most males leave the area after 2 years, associations may last for longer. Twenty dyads were observed associating over more than 2 years, for a maximum 5 years. One dyad was observed associating on 19 different days and clustered on 7 different days. Male associations may function to enhance foraging or to fend off predators. Such relationships seem to be adapted to a pelagic habitat with uncertain resource availability and predation pressure.


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