Swarming benthic crustaceans in the Bering and Chukchi seas and their relation to geographic patterns in gray whale feeding

1989 ◽  
Vol 67 (6) ◽  
pp. 1531-1542 ◽  
Author(s):  
Stacy L. Kim ◽  
John S. Oliver

Swarming benthic crustaceans were widespread in the Chukchi and Bering seas. Swarms differed in their geographic extent, local biomass, and life stages of swarming individuals and thus in their availability to feeding gray whales (Eschrichtius robustus). Immature amphipods apparently swarmed for dispersal, whereas cumaceans probably swarmed for mating. All life stages of the hyperbenthic mysids occurred above the sea floor. Although the geographic spread of mysid swarms and shrimp communities was much greater than for the amphipod and cumacean swarms, the latter swarmed in denser patches to produce higher local biomass. Crustacean swarms are important in describing the geographic patterns of gray whale feeding from the Chukchi Sea to Baja California, including the primary, secondary, and tertiary feeding grounds. The primary feeding ground is in the southern Chukchi Sea and especially the northern Bering Sea, where gray whales suck infaunal amphipods from fine sand, producing an extensive record of feeding excavations. The primary feeding ground is divided into a relatively deep zone (> 20 m), where tube-dwelling ampeliscid amphipods are the major prey, and a shallow zone (< 20 m), where burrowing pontoporeid amphipods dominate. The secondary feeding ground is in the southern Bering Sea along the eastern Alaska Peninsula and adjacent Alaskan mainland where shrimp and mysids are the major prey. The tertiary feeding ground is at the periphery of the primary and secondary feeding grounds in Alaskan waters and south of the Bering Sea where there is a general decrease in the availability of prey and their use by gray whales from Canada to Baja California. The tertiary prey communities include swarms of amphipods, cumaceans, and mysids as well as infaunal polychaete worms, but mysids are used the most by whales. The primary gray whale feeding ground was much smaller during low sea levels when the extensive Beringian Platform was exposed to air. This shallow shelf is a unique habitat that presently harbors the largest ampeliscid amphipod community in the world. At low sea level, swarming crustaceans like those sampled in the present study may have been equally or more important to gray whales than infaunal prey. These historical changes in prey availability may account for the catholic diet of the gray whale.

1984 ◽  
Vol 62 (1) ◽  
pp. 41-49 ◽  
Author(s):  
John S. Oliver ◽  
Peter N. Slattery ◽  
Mark A. Silberstein ◽  
Edmund F. O'Connor

Gray whales fed on dense populations of ampeliscid amphipods while summering along the west coast of Vancouver Island. These amphipod crustacean communities are ecological analogs of the primary feeding grounds of gray whales in the northern Bering Sea. The same major genera of amphipods dominated the Alaskan and Canadian feeding grounds, including Ampelisca, Photis, Protomedeia, Anonyx, and Orchomene, and comprised 67 to 90% of the number of infaunal crustaceans at the two locations. This is the first documented report of gray whale feeding on benthic infauna south of the Bering Sea. Feeding gray whales observed in Pachena Bay produced an extensive record of feeding excavations in bottom sediments. Excavation patterns suggest that: (i) whales used suction to extract infaunal prey and sediments; (ii) a maximum of six excavations was made in one feeding dive; (iii) excavation size was related to whale size; (iv) small and large whales fed in different parts of the bay; and (v) whales effectively located and worked the densest patches of benthic prey. We estimate that a 6-m whale consumed 116 kg of infaunal prey per 12-h day, and that a 12-m whale consumed 552 kg per 12-h day. Scavenging lysianassid amphipods were attracted to feeding disturbances within seconds and preyed on injured and dislodged infauna. Individual feeding excavations were large, deep valleys in a tube-mat plateau. In addition to the lysianassids, many other infauna undoubtedly colonize these highly modified habitats, resulting in important effects on the structure of benthic communities.


2021 ◽  
Vol 8 ◽  
Author(s):  
Lisa Hildebrand ◽  
Kim S. Bernard ◽  
Leigh G. Torres

Predators must consume enough prey to support costly events, such as reproduction. Meeting high energetic requirements is particularly challenging for migrating baleen whales as their feeding seasons are typically restricted to a limited temporal window and marine prey are notoriously patchy. We assessed the energetic value of the six most common nearshore zooplankton species collected within the Oregon, United States range of the Pacific Coast Feeding Group (PCFG) gray whale (Eschrichtius robustus) feeding grounds, and compared these results to the energetic value of the predominant amphipod species fed on by Eastern North Pacific (ENP) gray whales in the Arctic. Energetic values of Oregon zooplankton differed significantly between species (Kruskal–Wallis χ2 = 123.38, df = 5, p &lt; 0.0001), with Dungeness crab (Cancer magister) megalopae displaying the highest mean caloric content of all tested species (4.21 ± 1.27 kJ g– 1). This value, as well as the mean energetic value of the mysid Neomysis rayii (2.42 ± 1.06 kJ g– 1), are higher than the mean caloric content of Ampelisca macrocephala, the predominant Arctic amphipod. Extrapolations of these results to daily energetic requirements of gray whales indicate that lactating and pregnant gray whales feeding in the PCFG range would require between 0.7–1.03 and 0.22–0.33 metric tons of prey less per day if they fed on Dungeness crab megalopae or N. rayii, respectively, than a whale feeding on A. macrocephala in the Arctic. Yet, these results do not account for differences in availability of these prey species to foraging gray whales. We therefore suggest that other factors, such as prey density, energetic costs of feeding, or natal philopatry and foraging site fidelity play a role in the differences in population sizes between the PCFG and ENP gray whales. Climate change is implicated in causing reduced body condition and increased mortality of both PCFG and ENP gray whales due to decreased prey availability and abundance. Therefore, improved understanding of prey dynamics in response to environmental variability in both regions is critical.


2018 ◽  
Vol 44 (1) ◽  
pp. 7-12
Author(s):  
Amy L. Willoughby ◽  
Megan C. Ferguson ◽  
Janet T. Clarke ◽  
Amelia A. Brower

1962 ◽  
Vol 19 (5) ◽  
pp. 815-838 ◽  
Author(s):  
Gordon C. Pike

Observations of gray whales from the coasts of British Columbia, Washington, and Alaska are compared with published accounts in order to re-assess knowledge of migration and feeding of the American herd. Source of material is mainly from lighthouses and lightships.The American herd of gray whales retains close contact with the shore during migration south of Alaska. Off Washington and British Columbia the northward migration begins in February, ends in May, and is at a peak during the first two weeks in April; the southward migration occurs in December and January, and is at a peak in late December. Northward migrants stop occasionally to rest or feed; southward migrants are travelling faster and appear not to stop to rest or feed during December and January. Gray whales seen off British Columbia, sometimes in inside protected waters, from June through October, probably remain in this area throughout the summer and fall months.Available evidence suggests that gray whales retain contact with the coast while circumscribing the Gulf of Alaska, enter the Bering Sea through eastern passages of the Aleutian chain, and approach St. Lawrence Island by way of the shallow eastern part of the Bering Sea. Arriving off the coast of St. Lawrence Island in May and June the herd splits with some parts dispersing along the Koryak coast and some parts continuing northward as the ice retreats through Bering Strait. Gray whales feed in the waters of the Chukchi Sea along the Siberian and Alaskan coasts in July, August and September. Advance of the ice through Bering Strait in October initiates the southern migration for most of the herd. In summering areas, in northern latitudes, gray whales feed in shallow waters on benthic and near-benthic organisms, mostly amphipods.There is no evidence to indicate that gray whales utilize ocean currents or follow the same routes as other baleen whales in their migrations. Visual contact with coastal landmarks appear to aid gray whales in successfully accomplishing the 5000-mile migration between summer feeding grounds in the Bering and Chukchi Seas and winter breeding grounds in Mexico.Reconstruction of the migration from all available data shows that most of the American herd breeds and calves in January and February, migrates northward in March, April and May, feeds from June through October, and migrates southward in November and December.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Elena Schall ◽  
Karolin Thomisch ◽  
Olaf Boebel ◽  
Gabriele Gerlach ◽  
Sari Mangia Woods ◽  
...  

AbstractHumpback whale males are known to sing on their low-latitude breeding grounds, but it is well established that songs are also commonly produced ‘off-season’ on the feeding grounds or during migration. This opens exciting opportunities to investigate migratory aggregations, study humpback whale behavioral plasticity and potentially even assign individual singers to specific breeding grounds. In this study, we analyzed passive acoustic data from 13 recording positions and multiple years (2011–2018) within the Atlantic sector of the Southern Ocean (ASSO). Humpback whale song was detected at nine recording positions in five years. Most songs were recorded in May, austral fall, coinciding with the rapid increase in sea ice concentration at most recording positions. The spatio-temporal pattern in humpback whale singing activity on Southern Ocean feeding grounds is most likely shaped by local prey availability and humpback whale migratory strategies. Furthermore, the comparative analyses of song structures clearly show a differentiation of two song groups, of which one was solely recorded at the western edge of the ASSO and the other song group was recorded throughout the ASSO. This new finding suggests a common feeding ground occupation by multiple humpback whale populations in the ASSO, allowing for cultural and potentially even genetic exchange among populations.


1989 ◽  
Vol 67 (11) ◽  
pp. 2646-2654 ◽  
Author(s):  
Janet T. Clarke ◽  
Sue E. Moore ◽  
Donald K. Ljungblad

A total of 821 gray whales were seen during aerial surveys in the northeastern Chukchi Sea from July through October 1982–1987. Gray whale distribution extended from south of Point Hope to northeast of Point Barrow, Alaska, between 0.5 and 166 km offshore. Monthly abundance estimates (number of whales/survey hour) were highest in July (6.81) and lowest in October (0.40). Gray whales were usually in open water (82%, n = 670) or in light ice (16%, n = 134) and were seldom associated with heavy ice (2%, n = 17). Most whales were feeding (63%, n = 514), with the majority of the others swimming and diving (24%, n = 193) or forming part of a cow–calf association (9%, n = 72). One group of three whales was involved in sexual activity. Feeding whales were seen most often within 40 km of the shore, but also occurred offshore. Thirty-six gray whale calves were seen. Calf abundance (number of calves/survey hour) was significantly higher (p < 0.001) in July, when 92% (n = 33) of all calves were seen, than in any other month. Most cow–calf pairs were seen nearshore between Point Hope and Point Barrow. Monthly calf ratios (number of calves/number of whales) ranged from 0.09 in July to 0.00 in October, with an overall rate of 0.04.


ARCTIC ◽  
2016 ◽  
Vol 69 (4) ◽  
pp. 359 ◽  
Author(s):  
Janet T. Clarke ◽  
Amy S. Kennedy ◽  
Megan C. Ferguson

We analyzed data from line-transect aerial surveys for marine mammals conducted in the eastern Chukchi Sea (67˚–72˚ N, 157˚–169˚ W) in July to October of 2009–15 to investigate bowhead and gray whale distributions, behaviors, sighting rates, and habitat selection preferences, the last of which allowed direct comparison with results from data collected in this area in 1982–91. Bowhead whales use the eastern Chukchi Sea primarily for migrating between the Beaufort Sea and the Bering Sea, while gray whales use the area to feed on locally abundant benthic amphipods and other prey. Bowhead whales were observed during all survey months and were distributed up to 300 km offshore west and southwest of Point Barrow, Alaska, but without a defined migratory corridor in either summer (July-August) or fall (September-October). Bowhead whale sighting rates (whales per km on effort) were highest in the shelf/trough (51–200 m North) depth zone in the northeastern Chukchi Sea in both summer and fall. This pattern was reflected in habitat selection ratios, which found bowhead whales in summer and fall selecting primarily shelf/trough habitat in the northeastern Chukchi Sea, with shelf habitat (36 – 50 m) being preferred secondarily. Gray whales were observed in all survey months and were distributed primarily within ~95 km of shore between Point Barrow and Icy Cape in the northeastern Chukchi Sea, and about 60–115 km southwest of Point Hope in the southern Chukchi Sea. In both summer and fall, gray whale sighting rates and habitat selection ratios were highest in the shelf/trough (51–200 m South) depth zone in the southern Chukchi Sea. In the northeastern part of the study area, gray whale sighting rates and habitat selection ratios both identified coastal habitat (≤ 35 m) as preferred habitat in summer and shelf/trough (51–200 m North) as preferred habitat in fall. Distribution and habitat associations of bowhead and gray whales remained similar over the 34-year time span with one exception: gray whale preference for shelf/trough habitat in the southern Chukchi Sea is now evident throughout summer and fall, whereas three decades ago gray whale preference for that area was limited to fall only.


2021 ◽  
Vol 8 ◽  
Author(s):  
Jorge Urbán R ◽  
Esther Jiménez-López ◽  
Héctor M. Guzmán ◽  
Lorena Viloria-Gómora

Eastern gray whales undertake annual migrations between summer feeding grounds in the Bering and Chukchi Seas and winter breeding and calving lagoons in the west coast of Baja California, Mexico. On February 12, 2017, three adult gray whales were sighted at San José del Cabo, Mexico, in which one individual, named “María,” was tagged using a satellite telemetry transmitter (PTT). The PTT stopped the signal on July 11, 2017. María traveled 11,387 km during 149 days from San José del Cabo to the Chirikov Basin. The migration route was aligned close to the coastline (&lt;23 km) from February to April. After passing Kodiak Island in May, María started traveling far away from the coastline (&gt;70 km) into the Bering Sea, including the Chirikov Basin. During March, April, and May, María traveled long distances at relatively high speeds, in contrast to the lower speed during February, early March, and the arrival time to the feeding areas in May, June, and July. The total distance traveled by María during its migration from Ojo de Liebre Lagoon to the Chirikov Basin was 8,863 km during 61.5 days with an average speed of 5.5 km h–1; this excludes the 14 days and 591 km that María spent feeding on the coast of Kodiak Island in late April. The information provided by this tagged whale documents a single whales’ migration, which is consistent with previous studies and constitutes the most complete northbound reported migration of an eastern gray whale.


2017 ◽  
Vol 43 (6) ◽  
pp. 644-648
Author(s):  
César A. Salinas-Zavala ◽  
María V. Morales-Zárate ◽  
Andrés González-Peralta ◽  
Rosa J. Aviña-Hernández ◽  
Mariana L. Muzquiz-Villalobos

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