Cultural transmission, the social learning of information or behaviors from conspecifics, is believed to occur in a number of groups of animals, including primates, cetaceans, and birds. Cultural traits can be passed vertically (from parents to offspring), obliquely (from the previous generation via a nonparent model to younger individuals), or horizontally (between unrelated individuals from similar age classes or within generations). Male humpback whales (Megaptera novaeangliae) have a highly stereotyped, repetitive, and progressively evolving vocal sexual display or "song" that functions in sexual selection (through mate attraction and/or male social sorting). All males within a population conform to the current version of the display (song type), and similarities may exist among the songs of populations within an ocean basin. Here we present a striking pattern of horizontal transmission: multiple song types spread rapidly and repeatedly in a unidirectional manner, like cultural ripples, eastward through the populations in the western and central South Pacific over an 11-year period. This is the first documentation of a repeated, dynamic cultural change occurring across multiple populations at such a large geographic scale.
These datasets and accompanying syntheses provide a greater understanding of fundamental ecosystem processes in the Southern Ocean, support modelling of predator distributions under future climate scenarios and create inputs that can be incorporated into decision making processes by management authorities. In this data paper, we present the compiled tracking data from research groups that have worked in the Antarctic since the 1990s. The data are publicly available through biodiversity.aq and the Ocean Biogeographic Information System. The archive includes tracking data from over 70 contributors across 12 national Antarctic programs, and includes data from 17 predator species, 4060 individual animals, and over 2.9 million observed locations.Scientific Data | (2020) 7:94 | https://doi.org/10.1038/s41597-020-0406-x www.nature.com/scientificdata www.nature.com/scientificdata/ circum-Antarctic synthesis yet exists that crosses species boundaries. This deficiency prompted the Expert Group on Birds and Marine Mammals (EG-BAMM) and the Expert Group on Antarctic Biodiversity Informatics (EGABI) of the Scientific Committee on Antarctic Research (SCAR; www.scar.org) to initiate in 2010 the Retrospective Analysis of Antarctic Tracking Data (RAATD). RAATD aims to advance our understanding of fundamental and applied questions in a data-driven way, matching research priorities already identified by the SCAR Horizon Scan 9,21 and key questions in animal movement ecology 22 . For these reasons, we worked on the collation, validation and preparation of tracking data collected south of 45 °S. Data from over seventy contributors (Data Contacts and Citations 23 ) were collated. This database includes information from seventeen predator species, 4,060 individuals and over 2.9 million at-sea locations. To exploit this unique dataset, RAATD is undertaking a multi-species assessment of habitat use for higher predators in the Southern Ocean 24 .RAATD will provide a greater understanding of predator distributions under varying climate regimes, and provide outputs that can inform spatial management and planning decisions by management authorities such as the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR; www.ccamlr.org). Our synopsis and analysis of multi-predator tracking data will also highlight regional or seasonal data-gaps.Scientific Data | (2020) 7:94 | https://doi.
The responses of wild, non‐provisioned bottlenose dolphins (Tursiops truncatus) to swim attempts from commercial swim‐with‐dolphin tour boats were systematically observed during two research periods: 1994–1995 and 1997–1998. A total of 255 groups of dolphins was encountered during boat‐based surveys and 36% (n= 93) were exposed to at least one swim attempt. The operators' success with swim attempts, defined as at least one dolphin milling within 5 m of at least one swimmer, decreased from 48% in 1994–1995 to 34% in 1997–1998, and avoidance responses to swimmers increased from 22% to 31%. Dolphin response was found to vary according to swimmer placement. The greatest increase in avoidance occurred when swimmers were placed in the dolphins' path of travel. Based on sighting records of 266 individually identified dolphins, it was estimated that an average dolphin was exposed to 31 swim attempts per year. This level of exposure suggests that individual dolphins have, with cumulative experience, become sensitized to swim attempts. When a swim attempt was successful, on average it involved 19% of the group. Age‐class differences in interaction rates showed that juveniles were significantly more likely to interact with swimmers than adults. This study highlights the importance of longitudinal studies in evaluating human impact and suggests the urgent need for similar studies of potential human impact on other toothed cetaceans.
During the last 2 centuries, southern right whales Eubalaena australis were hunted to near extinction, and an estimated 150 000 were killed by pre-industrial whaling in the 19th century and illegal Soviet whaling in the 20th century. Here we focus on the coastal calving grounds of Australia and New Zealand (NZ), where previous work suggests 2 genetically distinct stocks of southern right whales are recovering. Historical migration patterns and spatially variable patterns of recovery suggest each of these stocks are subdivided into 2 stocks: (1) NZ, comprising NZ subantarctic (NZSA) and mainland NZ (MNZ) stocks; and (2) Australia, comprising southwest and southeast stocks. We expand upon previous work to investigate population subdivision by analysing over 1000 samples collected at 6 locations across NZ and Australia, although sample sizes were small from some locations. Mitochondrial DNA (mtDNA) control region haplotypes (500 bp) and microsatellite genotypes (13 loci) were used to identify 707 individual whales and to test for genetic differentiation. For the first time, we documented the movement of 7 individual whales between the NZSA and MNZ based on the matching of multilocus genotypes. Given the current and historical evidence, we hypothesise that individuals from the NZ subantarctic are slowly recolonising MNZ, where a former calving ground was extirpated. We also suggest that southeast Australian right whales represent a remnant stock, distinct from the southwest Australian stock, based on significant differentiation in mtDNA haplotype frequencies (F ST = 0.15, p < 0.01; Φ ST = 0.12, p = 0.02) and contrasting patterns of recovery. In comparison with significant differences in mtDNA haplotype frequencies found between the 3 proposed stocks (overall F ST = 0.07, Φ ST = 0.12, p < 0.001), we found no significant differentiation in microsatellite loci (overall
Humpback whales have a continually evolving vocal sexual display, or "song," that appears to undergo both evolutionary and "revolutionary" change. All males within a population adhere to the current content and arrangement of the song. Populations within an ocean basin share similarities in their songs; this sharing is complex as multiple variations of the song (song types) may be present within a region at any one time. To quantitatively investigate the similarity of song types, songs were compared at both the individual singer and population level using the Levenshtein distance technique and cluster analysis. The highly stereotyped sequences of themes from the songs of 211 individuals from populations within the western and central South Pacific region from 1998 through 2008 were grouped together based on the percentage of song similarity, and compared to qualitatively assigned song types. The analysis produced clusters of highly similar songs that agreed with previous qualitative assignments. Each cluster contained songs from multiple populations and years, confirming the eastward spread of song types and their progressive evolution through the study region. Quantifying song similarity and exchange will assist in understanding broader song dynamics and contribute to the use of vocal displays as population identifiers.
The conservation status of New Zealand (NZ) marine mammals (suborders Cetacea and Pinnipedia) is reappraised using the 2008 version of the NZ Threat Classification System. The list comprises 56 taxa (named species or subspecies, and as yet unnamed forms or types) in the following categories: Threatened*eight taxa (five Nationally Critical and three Nationally Endangered); Vagrant*six taxa; Migrant*20 taxa; and Data Deficient*13 taxa. A further nine taxa are listed as Not Threatened. Relative to the previous listing, the threat status of two species worsened: the NZ sea lion (Phocarctos hookeri) was uplisted to Nationally Critical and the bottlenose dolphin (Tursiops truncatus) was uplisted to Nationally Endangered. No species was considered to have an improved status. With the uplisting of the NZ sea lion and the continued listing of the Hector's dolphin (Cephalorhynchus hectori hectori) as Endangered and Maui's dolphin (C. hectori maui) as Nationally Critical, all three endemic NZ marine mammals are now considered threatened with extinction. We considered future research or management actions that would allow the downlisting of the eight taxa currently listed as Threatened.
Certain populations of killer whales Orcinus orca feed primarily or exclusively on marine mammals. However, whether or not baleen whales represent an important prey source for killer whales is debatable. A hypothesis by Springer et al. (2003) suggested that overexploitation of large whales by industrial whaling forced killer whales to prey-switch from baleen whales to pinnipeds and sea otters, resulting in population declines for these smaller marine mammals in the North Pacific and southern Bering Sea. This prey-switching hypothesis is in part contingent upon the idea that killer whales commonly attack mysticetes while they are in these high-latitude areas. In this study, we used photographic and sighting data from long-term studies of baleen whales in 24 regions worldwide to determine the proportion of whales that bear scars (rake marks) from killer whale attacks, and to examine the timing of scar acquisition. The results of this study show that there is considerable geographic variation in the proportion of whales with rake marks, ranging from 0% to > 40% in different regions. In every region, the great majority of the scars seen were present on the whales' bodies when the animals were first sighted. Less than 7% (9 of 132) of scarred humpback whales with multi-year sighting histories acquired new scars after the first sighting. This suggests that most killer whale attacks on baleen whales target young animals, probably calves on their first migration from low-latitude breeding and calving areas to high-latitude feeding grounds. Overall, our results imply that adult baleen whales are not an important prey source for killer whales in high latitudes, and therefore that one of the primary assumptions underlying the Springer et al. (2003) prey-switching hypothesis (and its purported link to industrial whaling) is invalid.
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