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1.
Amanda L. Bradford David W. Weller † Yulia V. Ivashchenko ‡ Alexander M. Burdin § Robert L. Brownell Jr .# 《Marine Mammal Science》2009,25(1):161-175
Western gray whales ( Eschrichtius robustus ) are critically endangered and anthropogenic threats, such as entanglement in fishing gear and collisions with vessels, may be acting to limit recovery of the population. Thus, examining the magnitude of such anthropogenic interactions using a scar-based approach is warranted. A multi-year (1995–2005) photo-identification study of western gray whales on their feeding ground off northeastern Sakhalin Island, Russia, has resulted in a large data set of digital and film images of 150 individuals. These images were reviewed and scored for anthropogenic scarring by recording the presence of visible scars resulting from fishing gear entanglement and vessel collisions in 21 defined body regions. In total, 20.0% ( n = 30) of whales identified during the study period had detectable anthropogenic scarring, with 18.7% ( n = 28) determined to have been previously entangled in fishing gear at least once and 2.0% ( n = 3) to have survived at least one vessel collision. These estimates are likely to be conservative given the nature of the photo-identification data set, but indicate that male and female western gray whales are subject to anthropogenic interactions. Future studies designed to systematically estimate the frequency and rates of anthropogenic events are needed and would have direct conservation and management implications. 相似文献
2.
Estimations of gray whale abundance have generally assumed that shore-based observers record all whales migrating through the viewing area during periods uncompromised by visibility. We tested the repeatability of data collected at the standard gray whale census site at Granite Canyon Marine Laboratory in central California by using pairs of observers maintaining independent sighting records. Proximal shore sites were occupied 6 d (60 h) in January 1986 where one team counted 845 whales in 427 groups while the other team counted 990 whales in 477 groups. A comparison of the records showed that the first team missed 290 whales seen by the second team, and the second team missed 204 whales seen by the first team. The total number of whales in the viewing area was calculated for each team by the Petersen estimate, using mutually sighted whale groups as "recaptures". On average, observers recorded only 79% of the whales. More whales (68%) were missed when entire groups of whales were not seen rather than when groups were undercounted (32%). Visibility did not appear to affect observed rates of missed whales. Whales migrating at intermediate distances from the shore were less often missed than were those > 6 km or < 1 km offshore. This count discrepancy test confirms that an uncorrected calculation of population size for gray whales based on sighting records from solitary observers will be underestimated. 相似文献
3.
Melba De Jesús Gisela Heckel Jeffrey M. Breiwick Stephen B. Reilly 《Marine Mammal Science》2014,30(2):674-690
Eastern Pacific gray whales were monitored off Ensenada, Mexico, during the southbound migration. The objectives were to determine southbound migration timing and width of the migration corridor during three seasons (2003–2006). Migration timing was determined by fitting a generalized additive model to the shore counts for each season and estimating the 10, 50, and 90 percentiles of the fitted curves. To estimate abundance from shore‐based counts, a probability density function for the shore based distances was estimated by a product of a gamma distribution fit to the boat survey distance data for 2006/2007 and a half‐normal detection function using combined data of the three seasons. The parameters of the gamma distribution were corrected to account for less boat survey effort carried out 20–40 km than 0–20 km from shore. The onset of the migration off Ensenada was in late December/early January and ended around 13 February. The median date was 23–26 January for the first and third season and a week early for the second season. Boat surveys indicated a wide (20 km) migration corridor but most gray whales traveled within 9.9 km from shore. The estimated total number of whales during watch hours was 2,298 (95% CI = 1,536–4,447). 相似文献
4.
Habitat utilization and prey species of Vancouver Island gray whales were investigated by (1) summarizing 26 yr of distribution and feeding data and (2) conducting intensive observations in Clayoquot Sound, Vancouver Island, from 1989 to 1996. Whale distribution and movements were monitored from March to November through systematic boat surveys and whale-watch sighting programs. Prey species were collected by suction hose and plankton net or determined through analysis of fecal samples. Gray whales utilized virtually all of the southern west coast of Vancouver Island over the 26-yr observation period. Distribution, prey species, and feeding behavior showed marked variability during any one season and between years. Some feeding areas were used on an annual basis, others with >10-yr intervals between use. Feeding occurred in shallow sand or mud bays, eel grass beds, kelp beds, in the open water column, and at the surface. Young whales appeared to utilize habitat and prey species differently than adults. Main prey species included herring eggs/larvae ( Clupea harengus pallasi ), crab larvae ( Cancer magister megalops, Pachycbeles spp. zoea), mysids ( Holmesimysis sculpta, Neomysis rayii, Acanthomysis spp.), amphipods ( Ampelisca spp., Atylus borealis ), and ghost shrimp ( Callianassa californiensis ). The definition and relative importance of specific feeding grounds and the study of human impacts on this population are complicated by its broad and variable use of habitat and prey species. 相似文献
5.
Mean body lengths of gray whale calves were found to increase linearly from 4.6 m at birth to 7 m by weaning at six mo. After weaning, rates of length increase diminish, with calves reaching 8 m by one yr of age and 9 m by two yr. Evaluations of the weights of nine gray whales as functions of their measured lengths and girths reduce the emphasis placed on fast-induced seasonal variations in girth by Rice and Wolman (1971). From birth weights of just under one metric ton, calves double their weights by three mo of age and double again by weaning at six mo. 相似文献
6.
In Clayquot Sound, British Columbia, gray whales (Eschrichtius robustus) forage primarily on mysids (Family Mysideae) and also on crab larvae (Family Porcellanidae) that are constrained to specific habitat, which relate to bathymetric depths. In this paper we characterize the interactions of gray whales and their prey by analyzing fine scale spatial‐temporal patterns in foraging gray whale distribution within a season. Kernel density estimators are applied to two seasons (1998 and 2002) of high‐resolution data on foraging by gray whales. By partitioning data from each foraging season into several time periods (12 in 1998 and 11 in 2002), using a temporal autocorrelation function, and generating kernel density estimated surfaces for each time period, it is possible to identify discrete areas of increasing and declining foraging effort. Our results indicate that gray whales forage on mysids throughout a season and opportunistically forage on crab larvae. The episodic crab larvae feeding may reduce, but not eliminate, pressure to mysid populations enabling mysids to reassemble swarms and continue to support gray whale foraging in the latter part of the season. Results suggest that when managing marine environments, gray whale populations require multiple and connected habitats for summer foraging. 相似文献
7.
Wayne L. Perryman Trevor Joyce David W. Weller John W. Durban 《Marine Mammal Science》2021,37(2):448-462
This paper describes the relationship between eastern North Pacific gray whale calf production and environmental conditions in the Pacific Arctic where they feed. The results show how interannual variation in sea ice cover in the Bering and Chukchi Seas along with broader indices of North Pacific climate, such as Pacific Decadal Oscillation (PDO) and North Pacific Index (NPI), are linked to variation in gray whale reproductive output. Estimates of gray whale calf production were derived from 23 consecutive years (1994–2016) of shore-based visual surveys conducted off California during the northward migration. PDO and NPI in combination with ice cover in the Bering and Chukchi Seas during the early phase of gestation appear to be important in explaining the observed variability in calf production. Of the 2,285 time series linear models evaluated, the model of best-fit included PDO(July), Ice(June), NPI(February), and explained 60% of the observed variability in calf production. After elimination of two data outliers in calf production estimates (2013 and 2014) a model including Ice(May), PDO(May), and NPI(July) explained 90% of the variability. We conclude that access to prey early in the gestation period is critical to reproductive success in this population and may be important for other capital breeding mammals. 相似文献
8.
Electrocardiogram (ECG) analyses of Holter monitor recordings from a young California gray whale were performed to determine ECG waveform characteristics, evaluate the heart rate pattern for sinus arrhythmia, obtain resting heart rates at known body masses as the whale increased in size, and compare those heart rates with predicted heart rates from allometric equations. The PR and QRS intervals (475 ± 35 msec, 208 ± 24 msec, respectively, n= 20) support the concept (Meijler et al. 1992) that atrioventricular transmission and ventricular excitation times do not increase linearly in very large mammals. A sinus arrhythmia pattern at rest (apneic heart rates of 15–25 beats per min [bpm] and eupneic heart rates of 34–40 bpm) is consistent with a relative eupneic tachycardia and apneic bradycardia during diving activity of whales. The heart rate-body mass measurements (35–24 bpm at body masses of 3,591-8,200 kg) in this study (1) extend the range of allometric heart rate and body mass data in mammals a full order of magnitude, to almost 10,000 kg, (2) support the use of allometric equations (based primarily on mammals <1,000 kg in body mass) in estimating resting heart rates in whales, and (3) demonstrate that previously reported heart rates in large whales are not representative of resting heart rate, probably secondary to circumstances during measurement. 相似文献
9.
David J. Rugh Marcia M. Muto Roderick C. Hobbs James A. Lerczak 《Marine Mammal Science》2008,24(4):864-880
Counts of migrating whales depend on accurate sightings data. In this study, teams of shore‐based observers independently tracked whale pods during the southbound migration of gray whales (Eschrichtius robustus) while a routine (“standard watch”) census was underway. A comparison of sighting records showed that time and location accuracy was limited to 45 s, 3° (magnetic) horizontally, and 0.0057° (0.2 reticles) vertically. Of 242 attempts to track whale groups, 72 failed, 120 were “good tracks,” and 83 qualified as “best tracks” because they had ≥8 sightings/pod, ≥16‐min observation time, and unequivocal matches to sightings in the standard watch during uncompromised visibility. Between paired tracking teams, 39 attempts to conduct concurrent tracks resulted in 21 “good tracks” with complete agreement in 71% of the cases. Of 133 comparisons between trackers and the standard watch, 43% of the pod‐size estimates were the same, but the standard watch overestimated 10% of the pods and underestimated 47%. Thus, according to results from tracking teams, pods recorded as size 1 by observers on the standard watch should be corrected by +0.6; pods of 2 by +0.5; pods of 3 by +0.8; and pods >3 (4–10) were overestimated and should be corrected by ?0.6. 相似文献
10.
A digital acoustic recording tag was used to examine the 3‐D orientation of gray whales feeding along the central British Columbia coast. A total of 96 feeding dives were recorded from six different whales. More than half (53.1%) of the whales' bottom time was spent rolled at an angle greater than 45°. Whales rolled an average of 2.9 times per feeding dive, and rolling behavior was often accompanied by a negative pitch angle. Out of 282 recorded rolls, 274 (97.2%) were to the right. Likewise, 98.5% of the total time spent rolled at an angle greater than 45° was spent rolled to the right. The gray whales in this study showed a significant right‐side bias on both an individual (P≤ 0.009) and group level (P < 0.001). Based on the findings of this study and previous reports of uneven baleen wear ( Kasuya and Rice 1970 ), it is proposed that gray whales exhibit a population‐wide right‐side rolling bias similar in character to the 90/10 split of right handedness in humans. 相似文献
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Some odontocetes possess unique features of the hyolingual apparatus that are involved in suction feeding. The hyoid bone and associated musculature generates rapid, piston‐like retraction, and depression of the hyoid and tongue. “Capture” suction feeders (e.g., Globicephala) use suction for capturing and swallowing prey. “Combination” feeders (i.e., Lagenorhynchus) use both raptorial feeding (to capture prey) and suction (to ingest prey). In “capture” suction feeders, features of the hyoid and skull have been attributed to creating suction (i.e., large surface area and mandibular bluntness). In addition to odontocetes, a mysticete, the gray whale (Eschrichtius robustus), is considered a benthic suction feeder. However, anatomical studies of purported suction‐feeding structures of the gray whale are lacking. In addition, few studies have utilized evolutionary approaches to understand the history of suction feeding in cetaceans. This study incorporates quantitative and qualitative hyoid and cranial data from 35 extant and 14 extinct cetacean species into a multivariate principal component analysis and comparative phylogenetic analyses. Conclusions from these analyses are that some commonly attributed features (i.e., ventral throat grooves and mandibular bluntness) and one principal component are significantly correlated with suction feeding. Finally, ancestral state reconstructions indicate that suction feeding likely evolved once, early in cetacean evolutionary history. 相似文献
13.
Wayne L. Perryman Meghan A. Donahue Jeffrey L. Laake Thomas E. Martin 《Marine Mammal Science》1999,15(2):426-445
We recorded the blows of gray whales during their southbound migration past central California in January 1994, 1995, and 1996, using thermal imaging sensors. For our sampling purposes, we defined day (0730–1630) and night (1630–0730) to coincide with the on/off effort periods of the visual counts being conducted concurrently. We pooled data across the three years of sampling and tested for diel variation in surfacing interval, pod size, offshore distance, migration rate, and swimming speed by comparing paired day/night means for samples collected within the respective 24-h period. We performed these tests using data from the entire migration period and then repeated the tests for samples collected prior to and after the approximate median migration date (15 January). Over the entire migration period we observed larger diurnal pod sizes (x?day= 1.75 ± 0.280, x?night= 1.63 ± 0.232) and greater diurnal offshore distances (x?day= 2.30 ± 0.328 km, x?night= 2.03 ± 0.356 km) but found no diel variation in surfacing interval. For the entire migration period, the nocturnal migration rate (average number of whales passing per hour) was higher than the diurnal rate. During the first half of the migration we detected no diel variation in pod size or surfacing interval, but diurnal offshore distances were larger than at night (x?day= 2.28 ± 0.273 km, x?night= 1.96 ± 0.318 km). Diurnal and nocturnal migration rates prior to 15 January were not different. During the second half of the migration, there was no diel variation in surfacing interval, pod size, or distance offshore, but the nocturnal migration rate was higher (28%, SE = 11.6%) than the diurnal rate. We found no diel variation in swimming speed in any comparison. We propose that later migrants socialize more during the day, which effectively slows their diurnal rate of migration relative to nocturnal rates. 相似文献
14.
Behavior and diving patterns of summer resident gray whales ( Eschrichtius robustus ) foraging on mysids were studied in coastal bays along the north shore of Queen Charlotte Strait, British Columbia. In this region, gray whales were found to feed primarily on planktonic prey rather than on the benthos as in their primary feeding areas further north. During the summers of 1999 and 2000, whales spent most of their time actively feeding or searching for prey (77%), whereas only 15% of their time was spent traveling and 8% socializing. The majority of the dives were short; the mean dive duration was 2.24 min with approximately three respirations per surfacing and 15 s between blows. Whales dove frequently (26.7 h−1 ), spending only 17% of their time at the surface with an overall blow rate of 1.14 respirations per minute. Activity states were characterized by significantly different diving and respiratory parameters; feeding whales dove more frequently, with shorter intervals between respirations, thus spending less time at the surface compared to when traveling or searching. This diving pattern differs from benthic-feeding whales and likely optimizes capture of the mobile mysid swarms in shallow waters. 相似文献
15.
MICHELANGELO BISCONTI 《Zoological Journal of the Linnean Society》2008,153(1):161-186
A new eschrichtiid, Eschrichtioides gastaldii gen. nov., comb. nov. , is established based on a specimen previously assigned to Balaenoptera gastaldii Portis, 1885. The holotype is from the Early Pliocene of north-east Italy. It represents a fossil mysticete closely related to the living grey whale, Eschrichtius robustus . Comparative morphology and phylogenetic analysis support the monophyly of Eschrichtiidae and Cetotherium -like mysticetes and a sister group relationship between this clade and Balaenopteridae. Eschrichtiid fossils previously described are all from the Pleistocene and Late Pliocene while Eschrichtioides gastaldii is from the Early Pliocene. The recognition of this new eschrichtiid genus suggests that the Mediterranean trophic web of the Early Pliocene was more complex than at present and that the Neogene mysticete family-level biodiversity of the Mediterranean was higher than that currently observed in this basin. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society , 2008, 153 , 161–186. 相似文献
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ESTIMATED POPULATION SIZE OF THE CALIFORNIA GRAY WHALE 总被引：1，自引：0，他引：1
Abstract: The 1987-1988 counts of gray whales passing Monterey are reanalyzed to provide a revised population size estimate. The double count data are modeled using iterative logistic regression to allow for the effects of various covariates on probability of detection, and a correction factor is introduced for night rate of travel. The revised absolute population size estimate is 20,869 animals, with CV = 4.37% and 95% confidence interval (19,200, 22,700). In addition the series of relative population size estimates from 1967-1968 to 1987-1988 is scaled to pass through this estimate and modeled to provide variance estimates from interannual variation in population size estimates. This method yields an alternative population size estimate for 1987-1988 of 21,296 animals, with CV = 6.05% and 95% confidence interval (18,900, 24,000). The average annual rate of increase between 1967-1968 and 1987-1988 was estimated to be 3.29% with standard error 0.44%. 相似文献
18.
2011 年11 月5 日,福建省平潭县白青乡青峰村渔民出海作业时发现一头误撞定置刺网死亡的灰鲸,为福建省的首次灰鲸误捕案例,也是本世纪以来我国海域的首次灰鲸误捕记录。本文描述了该灰鲸的外形特征和骨骼系统,并报道外形和骨骼的测量数据。该灰鲸系雌性,体长1 309 cm,体重约21 t,为目前本种在我国海域搁浅/ 误捕记录中的最大个体。头骨长281 cm,宽128 cm,重250 kg;脊椎式为C7 + T13 + L13 +Ca23 = 56;指式为Ⅰ1,Ⅱ3,Ⅲ7,Ⅳ5,Ⅴ3;肋骨14 对,V 形骨10 枚。脊椎式、指式、肋骨和V 形骨较之以前的报道存在差异,说明灰鲸的脊椎式、指式、肋骨和V 形骨可能存在个体差异。此外,本文还综述了西北太平洋灰鲸目前所面临的主要致危因素。 相似文献
19.
In Clayoquot Sound, British Columbia, gray whales ( Eschrichtius robustus ) forage for pelagic, hyperbenthic, and benthic invertebrates. Prey types were collected near feeding whales and at sites where no whales were observed to ascertain whales' diets and to describe prey populations and distributions. Characteristics of prey that are examined include species composition, density, biomass, and size. Whales foraged for mysids, Holmesimysis sculpta being the most abundant species collected. Whales foraged near concentrated patches of porcelain crab zoeal larvae, composed primarily of Pachycheles rudis , 21 –294 times the average density and biomass normally collected. Amphipod biomass, composed primarily of Ampelisca agassizi and A. careyi , was 160 ± 150 g/m2 where whales foraged. Larger amphipods, rather than higher density, resulted in higher amphipod biomass between years. Whales foraged where there was a high proportion (61%) of amphipods > 6 mm in length. Whales initially foraged for amphipods along the 20-m depth contour line; amphipod biomass was best developed and least variable at depths between 16 and 20 m. 相似文献
20.
Wayne L. Perryman Meghan A. Donahue Peter C. Perkins Stephen B. Reilly 《Marine Mammal Science》2002,18(1):121-144
We conducted shore-based sighting surveys to estimate the number of northbound migrating gray whale calves passing Piedras Blancas, California, for seven consecutive years (1994–2000). In addition, we conducted aerial surveys to determine offshore distribution of the migration in 1994 and 1995, measured day/night migration rates with thermal sensors in 1994–1996, and maintained concurrent replicate watches near the peak of each migration to estimate the proportion of the cow/calf pairs missed by the standard watch team. During good weather, we counted 325, 194, 407, 501, 440, 141, and 96 calves during 1994–2000, respectively. Correcting these counts for periods not on watch and for calves missed, produced final estimates of 945 calves (SE = 68.21) for 1994, 619 calves (SE = 67.19) for 1995, 1,146 calves (SE = 70.67) for 1996, 1,431 calves (SE = 82.02) for 1997, 1,388 calves (SE = 91.84) for 1998, 427 calves (SE = 41.10) for 1999, and 279 calves (SE = 34.79) for 2000. Calf production indices (calf estimate/total population estimate) are 4.2%, 2.7%, 4.8%, 5.8%, 5.5%, 1.7%, and 1.1% for the years 1994–2000, respectively. Fluctuations in calf production over this time period were positively correlated with the length of time that primary feeding habitat was free of seasonal ice during the previous year. 相似文献