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1.
As part of a project comparing the structure and function of four marine ecosystems off Norway and the United States, this paper examines the oceanographic responses to climate forcing, with emphasis on recent changes. The four Northern Hemisphere ecosystems include two in the Pacific Ocean (Bering Sea and Gulf of Alaska) and two in the Atlantic Ocean (Georges Bank/Gulf of Maine and the Barents/Norwegian Seas). Air temperatures, wind forcing and heat fluxes over the four regions are compared as well as ocean hydrography and sea-ice conditions where seasonal sea ice is found. The long-term interannual variability in air temperatures, winds and net heat fluxes show strong similarity between adjacent ecosystems and within subregions of an ecosystem, but no significant correlations between Pacific and Atlantic ecosystems and few across the Atlantic. In spite of the lack of correlation between climate forcing and ocean conditions between most of the ecosystems, recent years have seen record or near record highs in air and sea temperatures in all ecosystems. The apparent causes of the warming differ. In the Atlantic, they appear to be due to advection, while in the Pacific temperatures are more closely linked to air-sea heat exchanges. Advection is also responsible for the observed changes in salinity in the Atlantic ecosystems (generally increasing salinity in the Barents and Norwegian Seas and decreasing in the Gulf of Maine and Georges Bank) while salinity changes in the Gulf of Alaska are largely related to increased local runoff.  相似文献   

2.
Major features of four marine ecosystems were analyzed based on a broad range of fisheries-associated datasets and a suite of oceanographic surveys. The ecosystems analyzed included the Gulf of Maine/Georges Bank in the Northwest Atlantic Ocean, the Norwegian/Barents Seas in the Northeast Atlantic Ocean, and the eastern Bering Sea and the Gulf of Alaska in the Northeast Pacific Ocean. We examined survey trends in major fish abundances, total system fish biomass, and zooplankton biomasses. We standardized each time series and examined trends and anomalies over time, using both time series and cross-correlational statistical methods. We compared dynamics of functionally analogous species from each of these four ecosystems. Major commonalities among ecosystems included a relatively stable amount of total fish biomass and the importance of large calanoid copepods, small pelagic fishes and gadids. Some of the changes in these components were synchronous across ecosystems. Major differences between ecosystems included gradients in the magnitude of total fish biomass, commercial fish biomass, and the timing of major detected events. This work demonstrates the value of comparative analysis across a wide range of marine ecosystems, suggestive of very few but none-the-less detectable common features across all northern hemisphere ocean systems.  相似文献   

3.
As part of the international MENU collaboration, we compared and contrasted ecosystem responses to climate-forced oceanographic variability across several high latitude regions of the North Pacific (Eastern Bering Sea (EBS) and Gulf of Alaska (GOA)) and North Atlantic Oceans (Gulf of Maine/Georges Bank (GOM/GB) and the Norwegian/Barents Seas (NOR/BAR)). Differences in the nitrate content of deep source waters and incoming solar radiation largely explain differences in average primary productivity among these ecosystems. We compared trends in productivity and abundance at various trophic levels and their relationships with sea-surface temperature. Annual net primary production generally increases with annual mean sea-surface temperature between systems and within the EBS, BAR, and GOM/GB. Zooplankton biomass appears to be controlled by both top-down (predation by fish) and bottom-up forcing (advection, SST) in the BAR and NOR regions. In contrast, zooplankton in the GOM/GB region showed no evidence of top-down forcing but appeared to control production of major fish populations through bottom-up processes that are independent of temperature variability. Recruitment of several fish stocks is significantly and positively correlated with temperature in the EBS and BAR, but cod and pollock recruitment in the EBS has been negatively correlated with temperature since the 1977 shift to generally warmer conditions. In each of the ecosystems, fish species showed a general poleward movement in response to warming. In addition, the distribution of groundfish in the EBS has shown a more complex, non-linear response to warming resulting from internal community dynamics. Responses to recent warming differ across systems and appear to be more direct and more pronounced in the higher latitude systems where food webs and trophic interactions are simpler and where both zooplankton and fish species are often limited by cold temperatures.  相似文献   

4.
《Oceanologica Acta》2002,25(5):213-218
Recent advances in physical oceanography, sampling and observation tools, and data management methods are sufficient to enable a wide range of organisms in the Gulf of Maine to be quantified and related both to other organisms and to the physical habitat. A pilot Census of marine life in the Gulf of Maine would advance the goals of ecosystem understanding and management in a timely manner. A prerequisite is knowledge of the distribution and abundance of the organisms that inhabit, both permanently and transiently, the Gulf of Maine and adjacent waters, namely those of Georges Bank, Browns Bank, and Slope Sea, including the New England seamounts. Both systematic and synoptic investigations of a spectrum of marine life are needed to supplement current data holdings, which, if extensive with respect to fish and certain marine mammals, are sparse with respect to the larger biogeography of the system. Technology offers the means of collecting and organizing such data. Efficiency in collection argues for dividing the spectrum of marine life into a number of functional groups, whose constituent organisms can be observed or sampled by the same or similar techniques. Five groups are identified: offshore subtidal benthos, intertidal and nearshore subtidal benthos, plankton, fish and squid, and large marine animals and seabirds. Associated tools of observation and sampling are listed and illustrated for two categories: high-frequency scientific echo sounders and underwater video microscopes. Parameters of the physical habitat are listed, and the power of the Gulf of Maine Ocean Observing System to define the physical oceanography is noted. Issues of data management, systems, and uses are described. Some benefits of a pilot census are noted. For the scientific community, these include making available biogeographic data that can support the formulation of data-based hypotheses. Testing these in the Gulf of Maine and adjacent waters may enable new knowledge of the particular ecosystem to be extended to distant ecosystems.  相似文献   

5.
Abundance and biomass of the most important fish species inhabited the Barents and Norwegian Sea ecosystems have shown considerable fluctuations over the last decades. These fluctuations connected with fishing pressure resulted in the trophic structure alterations of the ecosystems. Resilience and other theoretical concepts (top-down, wasp-waste and bottom-up control, trophic cascades) were viewed to examine different response of the Norwegian and Barents Sea ecosystems on disturbing forces. Differences in the trophic structure and functioning of Barents and Norwegian Sea ecosystems as well as factors that might influence the resilience of the marine ecosystems, including climatic fluctuation, variations in prey and predator species abundance, alterations in their regular migrations, and fishing exploitation were also considered. The trophic chain lengths in the deep Norwegian Sea are shorter, and energy transfer occurs mainly through the pelagic fish/invertebrates communities. The shallow Barents Sea is characterized by longer trophic chains, providing more energy flow into their benthic assemblages. The trophic mechanisms observed in the Norwegian Sea food webs dominated by the top-down control, i.e. the past removal of Norwegian Spring spawning followed by zooplankton development and intrusion of blue whiting and mackerel into the area. The wasp-waist response is shown to be the most pronounced effect in the Barents Sea, related to the position of capelin in the ecosystem; large fluctuations in the capelin abundance have been strengthened by intensive fishery. Closer links between ecological and fisheries sciences are needed to elaborate and test various food webs and multispecies models available.  相似文献   

6.
Molecular population genetic analysis has provided evidence that the copepod, Calanus finmarchicus, of the Labrador Current, Gulf of St Lawrence, Scotian Shelf, Gulf of Maine, and Georges Bank constitute a single, interbreeding population. The DNA sequence of a 350 base pair portion of the mitochondrial large subunit (16S) ribosomal RNA (rRNA) gene was determined for a total of 72 individuals collected in 1992, and 110 individuals collected in 1993 from these regions. There was significant heterogeneity in haplotype frequencies among the samples collected in 1992, but this heterogeneity did not resolve into regional patterns. The only regional differences seen were between pooled samples of the western N. Atlantic and those of the Norwegian Sea. There were no significant differences in haplotype frequencies among the samples collected in 1993, and fewer haplotypes were observed in these samples. Intraspecific molecular variation was typical of other marine species: there were 29 haplotypes among the 182 individuals sequenced. The frequency distribution of the haplotypes was highly skewed: 128 individuals shared one haplotype and 19 individuals were unique. There were 24 variable sites among the 350 bases sequenced; estimated nucleotide diversity was 0.0042. The genetic character of C. finmarchicus populations in the western N. Atlantic was stable over time in that three of the haplotypes (including the most abundant) occurred in both 1992 and 1993. However, haplotype frequencies differed significantly between the two years. The lack of regional structure in the 1992 samples and the genetic homogeneity of samples collected in 1993 across the domain from the Labrador Current to the Gulf of St Lawrence to Georges Bank and the Gulf of Maine indicated that there is significant gene flow across this region. The persistent genetic pattern suggests that the Gulf of St Lawrence may be an important source region for recruitment of C. finmarchicus to Georges Bank. Determination of zooplankton dispersal patterns within high gene flow species will provide information that may not be determined by conventional oceanographic analyses.  相似文献   

7.
Temporal and spatial patterns of recruitment (R) and spawning stock biomass (S) variability were compared among functionally analogous species and similar feeding guilds from six marine ecosystems. Data were aggregated into four regions including the Gulf of Maine/Georges Bank, the Norwegian/Barents Seas, the eastern Bering Sea, and the Gulf of Alaska. Variability was characterized by calculating coefficients of variation and anomalies for three response variables: ln(R), ln(R/S), and stock–recruit model residuals. Patterns of synchrony and asynchrony in the response variables were examined among and between ecosystems, between- and within-ocean basins and among functionally analogous species groups using pair-wise correlation analysis corrected for within-time series autocorrelation, multivariate cross-correlation analyses and regime shift detectors. Time series trends in response variables showed consistent within basin similarities and consistent and coherent differences between the Atlantic and Pacific basin ecosystems. Regime shift detection algorithms identified two broad-scale regime shift time periods for the pelagic feeding guild (1972–1976 and 1999–2002) and possibly one for the benthic feeding guild (1999–2002). No spatial patterns in response variable coefficients of variation were observed. Results from multivariate cross-correlation analysis showed similar trends. The data suggest common external factors act in synchrony on stocks within ocean basins but temporal stock patterns, often of the same species or functional group, between basins change in opposition to each other. Basin-scale results (similar within but different between) suggest that the two geographically broad areas are connected by unknown mechanisms that, depending on the year, may influence the two basins in opposite ways. This work demonstrates that commonalities and synchronies in recruitment fluctuations can be found across geographically distant ecosystems but biophysical causes of the fluctuations remain difficult to identify.  相似文献   

8.
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9.
The Continuous Plankton Recorder (CPR) survey has sampled plankton on 14 routes off the coasts of the northeast United States and Canada between 1959 and 2000. Six of these routes are still operating and are sampled on a monthly basis. Some 2047 CPR tows have been made to the end of 2000 and the resulting database represents the most extensive time series of marine plankton available anywhere in the northwest Atlantic. The location and time span of coverage of each route is presented. In addition selected information is presented on:
1. zooplankton abundance as departures from baselines for the northeast US continental shelf;
2. interannual variation in seasonality of Gulf of Maine phytoplankton;
3. zooplankton relationships to local hydrography of the Gulf of Maine and to the North Atlantic Oscillation;
4. time-space matrices of zooplankton abundance and anomalies southeast of New York City;
5. time series of phyto- and zooplankton on the Scotian Shelf;
6. seasonal cycles of Phytoplankton Colour and of zooplankton on the Scotian Shelf and Georges Bank, and in the Gulf of Maine; and
7. monthly abundance of zooplankton in Narragansett Bay, Rhode Island.
  相似文献   

10.
The principal features of the marine ecosystems in the Barents and Norwegian Seas and some of their responses to climate variations are described. The physical oceanography is dominated by the influx of warm, high-salinity Atlantic Waters from the south and cold, low-salinity waters from the Arctic. Seasonal ice forms in the Barents Sea with maximum coverage typically in March–April. The total mean annual primary production rates are similar in the Barents and Norwegian Seas (80–90 g C m−2), although in the Barents, the production is higher in the Atlantic than in the ice covered Arctic Waters. The zooplankton is dominated by Calanus species, C. finmarchicus in the Atlantic Waters of the Norwegian and Barents Seas, and C. glacialis in the Arctic Waters of the Barents Sea. The fish species in the Norwegian Sea are mostly pelagics such as herring (Clupea harengus) and blue whiting (Micromesistius poutassou), while in the Barents Sea there are both pelagics (capelin (Mallotus villosus Müller), herring, and polar cod (Boreogadus saida Lepechin)) and demersals (cod (Gadus morhua L.) and haddock (Melanogrammus aeglefinus)). The latter two species spawn in the Norwegian Sea along the slope edge (haddock) or along the coast (cod) and drift into the Barents Sea. Marine mammals and seabirds, although comprising only a relatively small percentage of the biomass and production in the region, play an important role as consumers of zooplankton and small fish. While top-down control by predators certainly is significant within the two regions, there is also ample evidence of bottom-up control. Climate variability influences the distribution of several fish species, such as cod, herring and blue whiting, with northward shifts during extended warm periods and southward movements during cool periods. Climate-driven increases in primary and secondary production also lead to increased fish production through higher abundance and improved growth rates.  相似文献   

11.
The mean seasonal cycle and distribution of various life history stages of C. finmarchicus throughout the Georges Bank (GB)-Gulf of Maine (GOM) region were characterized based on 5966 MARMAP zooplankton samples collected during 106 surveys over a 10-year period (autumn 1977–autumn 1987). A high degree of seasonal and spatial variability in C. finmarchicus abundance throughout the region was evident in contoured portrayals of data, grouped into standard stations and 2-month “seasons”.Eight subareas of the Gulf of Maine-Georges Bank region were identified through cluster analysis of standard stations having similar seasonal patterns in mean abundance of C. finmarchicus stages C3, C4, C5 and adults. These were the northern Gulf of Maine (Northern GOM); southern Gulf of Maine (Southern GOM); Scotian Shelf-coastal Gulf of Maine (Scotian-Coastal GOM); Mass Bay; tidally mixed Georges Bank (Mixed GB); tidal front on the Bank separating mixed from seasonally stratified water (Tidal Front GB); seasonally stratified water on the Bank (Stratified GB) and the Continental Slope adjacent to Georges Bank (SLOPE).A distinct seasonal abundance cycle was present in all subareas, but, the magnitude and timing of annual maxima varied greatly among subareas. Peak abundance was reached early (March–April) in Mixed GB, Tidal Front GB and Mass Bay, and late (July–August) in Northern GOM and Scotian-Coastal GOM. Remaining subareas had maxima in May–June. Abundance increased 10-fold from January–February to March–April and decreased sharply from July–August to September–October in all areas except southern GOM and northern GOM. The amplitude of the annual cycle was weakest in northern GOM and southern GOM, where high concentrations of C. finmarchicus persisted year-round, and strongest in the tidally mixed shallow water on GB, where the sparsest densities of C. finmarchicus occurred most of the year. Abundance curves for the various areas converged in March–April, when C. finmarchicus was ubiquitously very abundant (> 104/10 m2), and diverged from September to December.C. finmarchicus stage distribution in the GB-GOM area was highly negatively correlated with mean water column temperature during the stratified season. This seemed more related to the hydrography of the region, which isolates warmer well mixed Georges Bank from the Gulf of Maine and the stratified areas on the Bank, than to temperature, because Calanus abundances decline on the Bank before water temperatures exceed their preferences.A large part of the spatial and seasonal variation in C. finmarchicus abundance and age structure appears to be tightly coupled to major hydrographic regimes and to major circulation patterns in the region. There was a sharp ecotone between well-mixed Georges Bank and the Gulf of Maine as defined by C. finmarchicus abundance patterns and life history distributions. The ecotone is present year-round but is most apparent during the stratified season (May–October), when thermohaline density gradients and the near-surface current jet along the northern flank are generally strongest. The Gulf of Maine had the highest abundances of C. finmarchicus, and lowest spatial and seasonal variation in the region, while tidally mixed Georges Banks displayed the opposite pattern. This indication of stable population centers in the Gulf of Maine would make it a major source of Calanus in the region, particularly during March–April. Distributional patterns also suggest a strong Calanus influence from Scotian Shelf water in northern Gulf of Maine and on the southern flank of Georges Bank.  相似文献   

12.
Populations of the copepod species Calanus finmarchicus often dominate the springtime biomass and secondary production of shelf ecosystems throughout the North Atlantic Ocean. Recently, it has been hypothesised that interannual to interdecadal fluctuations observed in such populations are driven primarily by climate-associated changes in ocean circulation. Here, we compare evidence from the North Sea and Gulf of Maine/Western Scotian Shelf (GoM/WSS) linking fluctuations in C. finmarchicus abundance to changes in ocean circulation associated with the North Atlantic Oscillation (NAO). A particularly striking contrast emerges from this Trans-Atlantic comparison: whereas the North Sea C. finmarchicus population exhibits a negative correlation with the NAO index, the GoM/WSS population exhibits a more complex, positive association with the index. The physical processes underlying these contrasting population responses are discussed in the context of regional- to basin-scale circulation changes associated with the NAO.  相似文献   

13.
The past 50 years in the Gulf of Maine and Georges Bank is marked by a growing divide between fishermen, scientists, and managers. This paper tracks the scientific, regulatory, social and political evolution of fisheries management in the Northwest Atlantic, culminating in a distrustful and adversarial climate, a convergence of diverse policy needs, and the emergence of a multi-stakeholder cooperative research program—the Northeast Consortium. The institutional structure and activities of the Northeast Consortium are presented and we conclude with a discussion of the role of cooperative research in building mutual understanding and respect, trust and scientific legitimacy.  相似文献   

14.
1IntroductionThe Beibu Gulf is a natural semiclosed conti-nental sea of the South China Sea,which is situatedat17°00′~21°45′N,105°40′~110°10′E,and sur-rounded by China and Vietnam(see Fig.1).It hasa subtropic monsoon climate with an average winter  相似文献   

15.
Impacts of climate change on commercial fish stocks in Norwegian waters   总被引：1，自引：0，他引：1  
The Norwegian fishing areas extend over various marine ecosystems that will respond differently to climate change. In the North Sea the productivity of the boreal fish species are likely to decrease under global warming and new warm-water species are expected to become more abundant. In the arctic marine ecosystem of the Barents Sea the fish productivity is expected to increase and their distributions expand northward and eastward under global warming increasing the importance of the Russian as well as the Norwegian sectors of the Barents. In the past, decadal-scale climate variations have been shown to strongly influence productivity and distributions of fish stocks. The importance of such shorter-term variations are expected to continue also under global warming. Under global warming the optimum temperature for fish farming along the Norwegian coast will be displaced northwards from the northern part of West Norway towards the Helgeland coast.  相似文献   

16.
Dense water formation and circulation in the Barents Sea   总被引：1，自引：0，他引：1  
Dense water masses from Arctic shelf seas are an important part of the Arctic thermohaline system. We present previously unpublished observations from shallow banks in the Barents Sea, which reveal large interannual variability in dense water temperature and salinity. To examine the formation and circulation of dense water, and the processes governing interannual variability, a regional coupled ice-ocean model is applied to the Barents Sea for the period 1948-2007. Volume and characteristics of dense water are investigated with respect to the initial autumn surface salinity, atmospheric cooling, and sea-ice growth (salt flux). In the southern Barents Sea (Spitsbergen Bank and Central Bank) dense water formation is associated with advection of Atlantic Water into the Barents Sea and corresponding variations in initial salinities and heat loss at the air-sea interface. The characteristics of the dense water on the Spitsbergen Bank and Central Bank are thus determined by the regional climate of the Barents Sea. Preconditioning is also important to dense water variability on the northern banks, and can be related to local ice melt (Great Bank) and properties of the Novaya Zemlya Coastal Current (Novaya Zemlya Bank). The dense water mainly exits the Barents Sea between Frans Josef Land and Novaya Zemlya, where it constitutes 63% (1.2 Sv) of the net outflow and has an average density of 1028.07 kg m−3. An amount of 0.4 Sv enters the Arctic Ocean between Svalbard and Frans Josef Land. Covering 9% of the ocean area, the banks contribute with approximately 1/3 of the exported dense water. Formation on the banks is more important when the Barents Sea is in a cold state (less Atlantic Water inflow, more sea-ice). During warm periods with high throughflow more dense water is produced broadly over the shelf by general cooling of the northward flowing Atlantic Water. However, our results indicate that during extremely warm periods (1950s and late 2000s) the total export of dense water to the Arctic Ocean becomes strongly reduced.  相似文献   

17.
Ocean policies around the world increasingly emphasize the importance of maintaining resilient ocean ecosystems, communities, and economies. To maintain and restore the resilience of healthy marine ecosystems in practice, specific management objectives with metrics and a policy framework for how to apply them will be needed. Here we present a concept for doing this, based on evidence that marine ecosystems transition from desirable to less desirable states in response to a number of physical, chemical, and biological drivers. More empirical and synthesis research will be necessary to develop quantitative metrics of resilience and thresholds between ecosystem states for specific ecosystems; however, suggestions are provided here for how to manage for resilience when insufficient data and knowledge are available for quantification. A summary of thresholds for biotic and abiotic drivers of ecosystem state drawn from the literature is also provided as a guide to management.  相似文献   

18.
The Barents Sea ecosystem has been associated with large biomass fluctuations. If there is a hidden deterministic process behind the Barents Sea ecosystem, we may forecast the biomass in order to control it. This presentation concludes, for the first time, investigations of a long data series from North Atlantic water and the Barents Sea ecosystem. The analysis is based on a wavelet spectrum analysis from the data series of annual mean Atlantic sea level, North Atlantic water temperature, the Kola section water temperature, and species from the Barents Sea ecosystem.The investigation has identified dominant fluctuations correlated with the 9.3-yr phase tide, the 18.6-yr amplitude tide, and a 74-yr superharmonic cycle in the North Atlantic water, Barents Sea water, and Arctic data series. The correlation between the tidal cycles and dominant Barents Sea ecosystem cycles is estimated to be R=0.6 or better. The long-term mean fluctuations correlate with the 74-yr superharmonic cycle. The wavelets analysis shows that the long-term 74-yr cycle may introduce a phase reversal in the identified 18-yr periods of temperature and salinity. The present analysis suggests that forced vertical and horizontal nodal tides influence the ocean's thermohaline circulation, and that they behave as a coupled non-linear oscillation system.The Barents Sea ecosystem analysis shows that the biomass life cycle and the long-term fluctuations correlate better than R=0.5 to the lunar nodal tide spectrum. Barents Sea capelin has a life cycle related to a third harmonic of the 9.3-yr tide. The life cycles of shrimp, cod, herring, and haddock are related to a third harmonic of the 18.6-yr tide. Biomass growth was synchronized to the lunar nodal tide. The biomass growth of zooplankton and shrimp correlates with the current aspect of lunar nodal tidal inflow to the Barents Sea. The long-term biomass fluctuation of cod and herring is correlated with a cycle period of about 3×18.6=55.8 yr. This analysis suggests that we may understand the Barents Sea ecosystem dynamic as a free-coupled oscillating system to the forced lunar nodal tides. This free-coupled oscillating system has a resonance related to the oscillating long tides and the third harmonic and superharmonic cycles.  相似文献   

19.
Sediments from 19 stations in the Gulf of Maine were analyzed for 16 priority polycyclic aromatic hydrocarbon (PAH) compounds in 1983. Thirteen of the compounds were distributed widely with total concentrations ranging from 10–512 ppb (dry wt). These values are an order of magnitude lower than those observed in the coastal zone but higher than those on Georges Bank. PAH concentration was directly related to grain size, total organic carbon (TOC) and distance from source. PAHs appear to be accumulating in Wilkinson and Jordan Basins but not in Georges Basin. Observed PAH distributions support the conclusion that the principal transport mechanism is through the atmosphere with localized augmentation by sediment resuspension and transport from coastal embayments.  相似文献   

20.
Atlantic Water flow through the Barents and Kara Seas   总被引：2，自引：0，他引：2  
The pathway and transformation of water from the Norwegian Sea across the Barents Sea and through the St. Anna Trough are documented from hydrographic and current measurements of the 1990s. The transport through an array of moorings in the north-eastern Barents Sea was between 0.6 Sv in summer and 2.6 Sv in winter towards the Kara Sea and between zero and 0.3 Sv towards the Barents Sea with a record mean net flow of 1.5 Sv. The westward flow originates in the Fram Strait branch of Atlantic Water at the Eurasian continental slope, while the eastward flow constitutes the Barents Sea branch, continuing from the western Barents Sea opening.About 75% of the eastward flow was colder than 0°C. The flow was strongly sheared, with the highest velocities close to the bottom. A deep layer with almost constant temperature of about −0.5°C throughout the year formed about 50% of the flow to the Kara Sea. This water was a mixture between warm saline Atlantic Water and cold, brine-enriched water generated through freezing and convection in polynyas west of Novaya Zemlya, and possibly also at the Central Bank. Its salinity is lower than that of the Atlantic Water at its entrance to the Barents Sea, because the ice formation occurs in a low salinity surface layer. The released brine increases the salinity and density of the surface layer sufficiently for it to convect, but not necessarily above the salinity of the Atlantic Water. The freshwater west of Novaya Zemlya primarily stems from continental runoff and at the Central Bank probably from ice melt. The amount of fresh water compares to about 22% of the terrestrial freshwater supply to the western Barents Sea. The deep layer continues to the Kara Sea without further change and enters the Nansen Basin at or below the core depth of the warm, saline Fram Strait branch. Because it is colder than 0°C it will not be addressed as Atlantic Water in the Arctic Ocean.In earlier decades, the Atlantic Water advected from Fram Strait was colder by almost 2 K as compared to the 1990s, while the dense Barents Sea water was colder by up to 1 K only in a thin layer at the bottom and the salinity varied significantly. However, also with the resulting higher densities, deep Eurasian Basin water properties were met only in the 1970s. The very low salinities of the Great Salinity Anomaly in 1980 were not discovered in the outflow data. We conclude that the thermal variability of inflowing Atlantic water is damped in the Barents Sea, while the salinity variation is strongly modified through the freshwater conditions and ice growth in the convective area off Novaya Zemlya.  相似文献   

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