scholarly journals Composition and structure of plankton communities in the Bering Sea

2021 ◽  
Vol 201 (1) ◽  
pp. 158-176
Author(s):  
K. M. Gorbatenko

On the data of long-term surveys, mean biomass of plankton in the epipelagic layer of the Bering Sea is evaluated as 821.3 mg/m3 (1058.2 mg/m3 in shelf areas and 760.6 mg/m3 in the deep-water areas) and the stock as 245.1•106 t WW (64.4 • 106 t over the shelf and 180.7 • 106 t in the deep-water sea). By taxa, the average annual portions are: 55.1 % for copepods, 26.3 % for arrowworms, 10.8 % for euphausiids, 3.2 % for medusas, and 2.9 % for amphipods. The dominant species are the arrowworm Sagitta elegans (26.3 %) and the copepod Eucalanus bungii (19.7 %); other mass species are: large-sized copepods Neocalanus cristatus (10.4 %), Neocalanus plumchrus + Neocalanus flemingeri (7.8 %) and Calanus glacialis + Calanus marshallae (5.1 %), euphausiids Thysanoessa raschii (3.5 %) and Thysanoessa longipes (3.4 %), small-sized copepods Metridia pacifica (3.5 %) and Oithona similis (3.5 %), medusa Aglantha digitale (3.2 %).

2014 ◽  
Vol 178 (3) ◽  
pp. 58-67
Author(s):  
Igor V. Volvenko

The Bering Sea, ​​Okhotsk Sea, Japan/East Sea and adjacent waters of the Pacific Ocean (mainly within EEZ of Russia) are compared by abundance of pelagic and benthic macrofauna, its species richness, evenness, diversity, and mean weight of animals using the data of long-term large-scale pelagic and bottom trawl surveys conducted by Pacific Fish. Res. Center (TINRO) in 1977-2010.


Author(s):  
Philip Blackmar ◽  
Ronald McPherson

St. George Island, Alaska is located in the Bering Sea more than 320 kilometers (200 miles) north of the nearest Aleutian Island. During original design and construction of the fishing harbor at St. George Island in the early 1980’s, stone large enough for a conventional breakwater was not available to quarry on the island, so the project utilized a berm breakwater approach with the available local stone. The long-term performance and service life of the berm breakwaters is reviewed in this paper. Construction of the berm breakwater was completed in 1987 and the breakwaters remained functional for nearly 20 years with little maintenance. In the winter of 2015/2016, approaching 30 years since initial construction, significant damage occurred during a winter storm. Repairs utilized a berm breakwater approach similar to the original design. Repairs were completed in 2 phases due to the short construction seasons at the project site.


2015 ◽  
Vol 8 ◽  
Author(s):  
Michel E. Hendrickx

The deep-water mysidCeratomysis spinosaFaxon, 1893, previously known from Panama, Japan, the Sea of Okhotsk, the Bering Sea and Alaska, USA is reported for the first time off the western coast of Mexico, in the eastern Pacific. The specimens, a male of 27.5 mm in total length (TL) and five females of 28.5–34.5 mm TL, were collected between depths of 1296 and 1580 m. The telson is illustrated, showing numerous setae on the lateral margins, and longer, robust setae in the distal third and on the posterior margin.


2019 ◽  
Vol 59 (6) ◽  
pp. 920-927
Author(s):  
V. V. Plotnikov ◽  
N. M. Vakulskaya ◽  
V. A. Dubina

Various aspects of seasonal and interannual variability of the sea ice cover are estimated on the basis of all available the Bering Sea ice data from 1960 to 2017. The possibility of long-term and superlong-term modeling of the ice cover is investigated. Results of tests are given, and a conclusion about prospects of the proposed model and an opportunity of its practical application is done.


2018 ◽  
Vol 195 ◽  
pp. 28-47
Author(s):  
A. O. Zolotov ◽  
O. A. Maznikova ◽  
A. Yu. Dubinina

Despite the long history of studies, some aspects of the greenland halibut biology in the North Pacifc are still poorly known. In particular, scientifc publications on its groupings in the Bering Sea and at the continental slope of the North Pacifc and their dynamics are rather few, with exception of the western Bering Sea area from Cape Olyutorsky to the Anadyr Bay where its dynamics is well traced by surveys of Pacifc Fish. Res. Center (TINRO). All data on long-term dynamics of the greenland halibut abundance and distribution in the Bering Sea and Pacifc waters at Kamchatka and Kuril Islands are overviewed and comparatively analyzed, including materials of bottom trawl surveys conducted in 1950–2015 and published research reports, in total the data of 66 surveys (4,350 bottom trawls) in the Karaginsky and Olyutorsky Bays, 43 surveys (4,900 trawls) on the Pacifc shelf and continental slope of Kamchatka and northern Kuril Islands, and 24 surveys (2,048 trawls) at southern Kuril Islands. Biomass of greenland halibut is assessed for the western Bering Sea and the Pacifc waters at Kamchatka and the Kuriles using the data of TINRO and for the eastern Bering Sea using the published data of NOAA and NPFMC. Gradual decreasing of commercial value of the halibut groups is shown with increase of the distance from its main spawning grounds in the southeastern Bering Sea. Self-reproduction of the halibut groups supposedly decreases in the same direction. This assumption is confrmed by the data on its larvae and juveniles density in the epipelagic layer of the western Bering Sea and North-West Pacifc that decreases from the maximum values in the Anadyr Bay to the Olyutorsko-Navarinsky district and further southward to the minimum value at southern Kuril Islands. The average portions of certain groups of greenland halibut in its total biomass in the North Pacifc (without the Okhotsk Sea) are estimated as follows: almost 85 % (146.0 . 103 t) is contributed by the southeastern Bering Sea, about 14 % (23.2 . 103 t) — by Olyutorsko-Navarinsky district and the Anadyr Bay, and 1% (about 1.5 . 103 t) — by the waters at northeastern and eastern Kamchatka and at Kuril Islands. Stock dynamics is similar for all groups: the stocks increased until the early 1970s with the peak in 1976–1980, when the species biomass was estimated as 280 . 103 t in the southwestern Bering Sea, 40 . 103 t in the Anadyr Bay and Olyutorsko-Navarinsky district, and 5 . 103 t in the bays of eastern Kamchatka and at northern Kuril Islands, then declined to the minimum in 1990–2000s, and recently the peripheral groups show a gradual growth. The dynamics similarity is possibly reasoned by passive transfer of the halibut eggs and larvae from the Bering Sea toward eastern Kamchatka and Kuril Islands by the system of oceanic currents.


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