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Detection of whale calls in noise: performance comparison between a beluga whale, human listeners, and a neural network.

This article examines the masking by anthropogenic noise of beluga whale calls. Results from human masking experiments and a software backpropagation neural network are compared to the performance of a trained beluga whale. The goal was to find an accurate, reliable, and fast model to replace lengthy and expensive animal experiments. A beluga call was masked by three types of noise, an icebreaker's bubbler system and propeller noise, and ambient arctic ice-cracking noise. Both the human experiment and the neural network successfully modeled the beluga data in the sense that they classified the noises in the same order from strongest to weakest masking as the whale and with similar call-detection thresholds. The neural network slightly outperformed the humans. Both models were then used to predict the masking of a fourth type of noise, Gaussian white noise. Their prediction ability was judged by returning to the aquarium to measure masked-hearing thresholds of a beluga in white noise. Both models and the whale identified bubbler noise as the strongest masker, followed by ramming, then white noise. Natural ice-cracking noise masked the least. However, the humans and the neural network slightly overpredicted the amount of masking for white noise. This is neglecting individual variation in belugas, because only one animal could be trained. Comparing the human model to the neural network model, the latter has the advantage of objectivity, reproducibility of results, and efficiency, particularly if the interference of a large number of signals and noise is to be examined.

Animals↗

In vitro metabolism of polychlorinated biphenyl congeners by beluga whale (Delphinapterus leucas) and pilot whale (Globicephala melas) and relationship to cytochrome P450 expression.

We measured rates of oxidative metabolism of two tetrachlorobiphenyl (TCB) congeners by hepatic microsomes of two marine mammal species, beluga whale and pilot whale, as related to content of selected cytochrome P450 (CYP) forms. Beluga liver microsomes oxidized 3,3',4,4'-TCB at rates averaging 21 and 5 pmol/min per mg for males and females, respectively, while pilot whale samples oxidized this congener at 0.3 pmol/min per mg or less. However, rates of 3,3',4,4'-TCB metabolism correlated with immunodetected CYP1A1 protein content in liver microsomes of both species. The CYP1A inhibitor alpha-naphthoflavone inhibited 3,3',4,4'-TCB metabolism by 40% in beluga, supporting a role for a cetacean CYP1A as a catalyst of this activity. Major metabolites of 3,3',4,4'-TCB generated by beluga liver microsomes were 4-OH-3,3',4',5-TCB and 5-OH-3,3',4,4'-TCB (98% of total), similar to metabolites formed by other species CYP1A1, and suggesting a 4,5-epoxide-TCB intermediate. Liver microsomes of both species metabolized 2,2',5,5'-TCB at rates of 0.2-1.5 pmol/min per mg. Both species also expressed microsomal proteins cross-reactive with antibodies raised against some mammalian CYP2Bs (rabbit; dog), but not others (rat; scup). Whether CYP2B homologues occur and function in cetaceans is uncertain. This study demonstrates that PCBs are metabolized to aqueous-soluble products by cetacean liver enzymes, and that in beluga, rates of metabolism of 3,3',4,4'-TCB are substantially greater than those of 2,2',5,5'-TCB. These directly measured rates generally support the view that PCB metabolism plays a role in shaping the distribution patterns of PCB residues found in cetacean tissue.

Animals↗

Measuring sperm whales from their clicks: stability of interpulse intervals and validation that they indicate whale length.

Multiple pulses can often be distinguished in the clicks of sperm whales (Physeter macrocephalus). Norris and Harvey [in Animal Orientation and Navigation, NASA SP-262 (1972), pp. 397-417] proposed that this results from reflections within the head, and thus that interpulse interval (IPI) is an indicator of head length, and by extrapolation, total length. For this idea to hold, IPIs must be stable within individuals, but differ systematically among individuals of different size. IPI stability was examined in photographically identified individuals recorded repeatedly over different dives, days, and years. IPI variation among dives in a single day and days in a single year was statistically significant, although small in magnitude (it would change total length estimates by <3%). As expected, IPIs varied significantly among individuals. Most individuals showed significant increases in IPIs over several years, suggesting growth. Mean total lengths calculated from published IPI regressions were 13.1 to 16.1 m, longer than photogrammetric estimates of the same whales (12.3 to 15.3 m). These discrepancies probably arise from the paucity of large (12-16 m) whales in data used in published regressions. A new regression is offered for this size range.

Acoustics↗

Killing times of minke whales in the Norwegian coastal whaling in the 1981 and 1982 seasons.

During the whaling seasons of 1981 and 1982 16 inspectors were on the whaling grounds to collect data about weapons and equipment, shooting facilities, hitting areas, reaction to hits, tissue and organ damage and killing times. The inspectors were instructed to confirm the criteria of death by personal observation before reading the time. Consequently the recorded times are appreciably longer than real killing time for a number of whales. The average killing time according to this method was 11 min 50 sec in the 1981 season and 12 min 40 sec in the 1982 season (Table I). 22.4% and 21.8% died instantaneously in the two seasons. Hitting the CNS or the heart was most effective. Hits in the abdominal cavity or the musculature prolonged the killing times considerably.

Animals↗

Neural and muscular control functions of the gut in odontocetes: morphologic evidence in beaked whales and beluga whales.

The present data provide some new and unique, gastrointestinal morphologic findings in two species of toothed whales, the Cuvier's beaked whale (Ziphius cavirostris) and the beluga or white whale (Delphinapterus leucas), which are discussed relative to their atypical feeding behavior and alimentary tract functions. Specifically, the findings show myenteric neural modifications and muscularis externa structural specializations which may support voluntary and involuntary fore- and hindgut behavior. Histologic evidence of intercalation-like striations in the gastric and colonic musculature was discovered, as well as an unusual massive size of the colonic myenteric plexuses. These observations, which are not evident in terrestrial mammalian gastrointestinal tracts, may help explain the unusual upper gastrointestinal tract motility such as ingestion-by-sucking in the absence of prehensile teeth and processing of ingesta in a multi-compartmentalized pyloric stomach. Further, the hindgut modifications may help explain the animal's acute, rectal discharge escape mechanism, likened to squid inking, which seems to be an evolved function of some cetaceans.

Animals↗

Chemical characterization of the oligosaccharides in Bryde's whale (Balaenoptera edeni) and Sei whale (Balaenoptera borealis lesson) milk.

Samples of milk from a Bryde's whale and a Sei whale contained 2.7 g/100 mL and 1.7 g/100 mL of hexose, respectively. Both contained lactose as the dominant saccharide along with small amounts of Neu5Ac(alpha2-3)Gal(beta1-4)Glc (3'-N-acetylneuraminyllactose), Neu5Ac(alpha2-6)Gal(beta1-4)Glc (6'-N-acetylneuraminyllactose) and Neu5Ac(alpha2-6)Gal(beta1-4)GlcNAc(beta1-3)Gal(beta1-4)Glc (LST c). The dominance of lactose in the carbohydrate of these milks is similar to that of Minke whale milk and bottlenose dolphin colostrum, but the oligosaccharide patterns are different from those of these two species, illustrating the heterogeneity of milk oligosaccharides among the Cetacea.

Animals↗

Modelling the past and future of whales and whaling.

Historical reconstruction of the population dynamics of whales before, during and after exploitation is crucial to marine ecological restoration and for the consideration of future commercial whaling. Population dynamic models used by the International Whaling Commission require historical catch records, estimates of intrinsic rates of increase and current abundance, all of which are subject to considerable uncertainty. Population genetic parameters can be used for independent estimates of historical demography, but also have large uncertainty, particularly for rates of mutational substitution and gene flow. At present, demographic and genetic estimates of pre-exploitation abundance differ by an order of magnitude and, consequently, suggest vastly different baselines for judging recovery. Here, we review these two approaches and suggest the need for a synthetic analytical framework to evaluate uncertainty in key parameters. Such a framework could have broad application to modelling both historical and contemporary population dynamics in other exploited species.

Journal Article↗

Distribution of sequence differences in influenza N9 neuraminidase of tern and whale viruses and crystallization of the whale neuraminidase complexed with antibodies.

Neuraminidase genes from A/tern/Australia/G70C/75 (H11N9) and A/whale/Maine/1/84 (H13N9) influenza viruses have been sequenced. Seventy-two nucleotide changes were found, 17 of which result in changes in the amino acid sequence of the neuraminidase; 3 in the stalk region and 14 in the heads. To our surprise, all of the sequence changes in the head region are located on the base of the neuraminidase tetramer, resulting in conservation of antigenic sites on top of the neuraminidase which vary extensively in human influenza virus neuraminidase. Whale N9 neuraminidase, like tern N9 neuraminidase, possesses high levels of hemagglutinating activity but, unlike the tern neuraminidase, failed to form large well-ordered crystals. However, when the neuraminidase was complexed with Fab fragments of monoclonal antibodies, which were made against the tern N9 neuraminidase, large crystals of the complexes were obtained which diffract X-rays to beyond 3 A.

Amino Acid Sequence↗