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1.
Bowhead whale ( Balaena mysticetus ) census data obtained during the northward spring migration are summarized for 1978–1983. Population size estimates are derived from counts made by observers standing on the seaward edge of shorefast ice in the vicinity of Point Barrow, Alaska, from mid-April to early June. The research design utilized two counting stations: South Perch, the primary counting station, and North Perch, used to determine the number of whales missed by South Perch observers. The percentage missed is estimated for each visibility category and used here to correct the census counts. Each season's population estimate is calculated as the sum of the number of trials of several independent multinomial distributions representing different visibility conditions. Corrections are applied for unwatched hours and hours with inferior visibility. A mean estimate of the number of whales passing within view of the census station was computed as 3,674 ± 299. This estimate was based on data collected in 1978, 1981, 1982, and 1983, years with the least apparent biases. Aerial survey data provide estimates of the proportion of whales passing at various distances seaward of the census sites as follows: 0.58 from the ice edge to 2 km, 0.76 to 3 km, and 0.80 to 4 km. Correcting for whales too far offshore to be seen by the ice-based observers results in a population estimate of over 4,200 bowheads.  相似文献   

2.
Under a U.S.-U.S.S.R. cooperative Marine Mammal Project, shipboard cruises were made in 1979, 1980 and 1982, primarily to determine whether there is a substock of western Arctic bowhead whales ( Balaena mysticetus ) that summers in the western Chukchi Sea instead of migrating to the Beaufort Sea. More than 100 bowheads were sighted along the north Chukotka coast of Siberia in October 1979, and more than 200 bowheads were sighted there in September 1980. None were seen anywhere in the Chukchi Sea in late July and August 1982. We conclude that the September and October sightings were of animals returning early from the Beaufort Sea and that, other than occurrences peripheral to the main migration, there are no large concentrations in the Chukchi in the summer and there is apparently no western Chukchi substock.  相似文献   

3.
Observations were made on 11 brains from bowhead whales subsistence-harvested by Alaskan Eskimos under International Whaling Commission guidelines. This study is part of a larger project to determine the basic morphology of this endangered species. The bowhead brain is similar to other cetacean brains, particularly that of the southern right whale. Long olfactory peduncles are reflected upon the rostrodorsal surface of the cerebral hemispheres. Olfactory bulbs have not been recovered but are presumed to exist since nerve fibers have been identified histologically in the olfactory peduncles. The induseum griseum is evident on the corpus callosum. The hippocampus proper is small but protrudes into the lateral ventricle. The cruciate sulcus runs diagonally across the rostral surface, limiting a small frontal lobe. The structure of the floor of the sylvian fissure varies from a few short gyri radiating toward the circular sulcus to a more extensive and complex two-tiered arrangement including numerous gyri perpendicular to the gyrus bordering the paleocortex. Pineal-body-like tissue was present in one specimen. There is no interthalamic adhesion. The lateral geniculate body is elevated but smaller than the large medial geniculate body. The neurohypophysis was adherent on most brain specimens received.  相似文献   

4.
The 2001 survey of western Arctic (Bering, Chukchi, and Beaufort seas) bowhead whales was conducted from 5 April to 7 June near Barrow, Alaska. Visual observers recorded a total of 3,295 “new” (not seen before) and 532 “conditional” (possibly seen before) whales in 1,130 h of watch effort, including 121 new calves (3.7% of the new whales). Concurrent with the visual survey, passive acoustic surveillance was conducted almost continuously from 16 April to 31 May, resulting in 27,023 locations of vocalizing bowhead whales. The estimated number of whales within 4 km of the perch (N4) was 7,025 (SE = 1,068). The estimated proportion of the whales within 4 km of the perch (P4) was 0.862 (SE = 0.044, computed by a moving blocks bootstrap). Combining these, the abundance estimate (N4/P4) for 2001 is 10,470 (SE = 1, 351) with a 95% confidence interval of 8, 100–13, 500. The estimated annual rate of increase (ROI) of the population from 1978 to 2001 is 3.4% (95% CI 1.7%‐5%). Reports from hunters and results of an aerial survey in June 2001 indicate whales continued to pass Barrow after the survey had ended. In 2001 51% (572 h) of the watch was scored as occurring during “fair‐excellent” visibility conditions, somewhat lower than the average for all surveys since 1978. Sea ice in the leads and fog were the principle environmental factors affecting visibility for all years. The estimated rate of increase and the fact that the number of calves counted in 2001 is the highest ever recorded suggest a steady recovery of this population. Other populations of large balaenids, notably the North Atlantic right whale, have failed to recover despite 70 yr of protection. The recovery of the howhead whale is likely attributable to low anthropogenic mortality, a relatively pristine habitat, and a well‐managed subsistence hunt. Nonetheless, offshore oil development, increasing shipping traffic, changes in the Bering Sea ecosystem, sea ice retreat, and possibly killer whale predation within its range could impact this bowhead population and should be carefully monitored.  相似文献   

5.
This paper compares the behavior of bowhead whales of the Davis Strait/Baffin Bay stock, as observed along the east coast of Baffin Island in 1979–1986, with behavior of the Bering/Chukchi/Beaufort Sea stock observed in the Beaufort Sea in 1980–1986. All data used here were collected during late summer and early autumn in the absence of acute human disturbance. The behavioral repertoires of the two populations were similar. However, quantitative differences were found for whales engaged in all three activities studied: (1) Bowheads feeding in deep water off Isabella Bay, Baffin Island, had longer dives and surfacings, on average, than noted for bowheads feeding in the Beaufort Sea. (2) Among whales socializing in shallow water, we saw sexual interactions more often at Isabella Bay than in the Beaufort Sea. Calls emitted by socializing whales off Baffin Island were similar to those heard in the Chukchi and Beaufort Seas. However, pulsed tonal calls were longer off Baffin Island, and previously undescribed mechanical "crunch" sounds were recorded there near socializing bowheads. (3) During autumn migration, "fluke-out" dives were less common, and dive durations were longer, in the Beaufort Sea than off Baffin Island (P<0.001). Multivariate and other analyses indicated that some but not all differences can be ascribed to regional differences in the natural environment or in whale activities, However, during 1974–1986, Bering/Chukchi/Beaufort bowheads were exposed to more industrial, hunting and other human activity than Davis Strait/Baffin Bay bowheads. The "inconspicuous" behavior during autumn migration in the Beaufort may have been attributable to human activities, but causative links cannot be isolated.  相似文献   

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