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1.
Concentrations of total carbonate, alkalinity and dissolved oxygen were obtained near the 1973 GEOSECS stations in the North Pacific subpolar region north of 40°N along 175°E between 1993 and 1994. A difference of excess CO2 content between the GEOSECS and our expeditions was estimated. The maximum difference in water column inventory of excess CO2 has increased by about 280 gC m–2 above 2000 m depth which apparently means an uptake of excess CO2 taken from air to sea during the last two decades. An averaged value of the annual flux of excess CO2 at 75–1000 m depth was 8.63±2.01 gC m–2yr–1 in the North Pacific subpolar region. By introducing the annual flux of excess CO2 into a two-box model for the North Pacific subpolar region, a penetration factor of excess CO2 from air to sea was obtained to be 1.08×10–2 gC m–3ppm–1 in the North Pacific subpolar region. Based on this factor, the surface concentration of excess CO2 in the North Pacific subpolar region was estimated to be 68 mole I–1, suggesting that the North Pacific subpolar region absorbed atmospheric excess CO2 more than the saturated concentration of excess CO2. Total amount of excess CO2 taken from the North Pacific subpolar region by 1993 was estimated to be 36.2×1015 gC, which was equal to about one tenth of that released by human activities after the preindustrial era.  相似文献   

2.
Recent carbonate data collected in the North Pacific were combined with the data in the literature in order to understand more clearly the carbonate chemistry in the North Pacific. Our analyses show that inorganic CaCO3 dissolution contributes about 26% of the total inorganic CO2 increase of deep water, after leaving the Southern Ocean. The calcium and alkalinity data indicate a CaCO3 dissolution rate of 0.060±0.010 and 0.053±0.005 µ mol kg–1 yr–1 respectively, for waters deeper than 2,000 m in reference to the Weddell Sea Deep Water. The organic carbon decomposition rate is 0.107±0.012 µ mol kg–1 yr–1 while the oxygen consumption rate is 0.13±0.002 µ mol kg–1 yr–1. These results which are based on the direct comparison of two water masses agree well with other estimates which are based on methods such as the one-dimensional-diffusion-advection model. Comparison of data along the two sections at 165°E and 150°W shows no significant difference in the ratio of the CaCO3 dissolution rate and the organic carbon decomposition rate. The eastern section, however, has a higher TCO2 input than the western section because of the older age of the deep water along the eastern section.  相似文献   

3.
Time-series measurements of dissolved inorganic carbon (DIC) and nutrient concentrations were conducted in the northwestern North Pacific from October 2002 to August 2004. Assuming that data obtained in different years represented time-series seasonal data for a single year, vertical distributions of DIC and nutrients showed large seasonal variabilities in the surface layer (∼100 m). Seasonal variabilities in normalized DIC (nDIC) and nitrate concentrations at the sea surface were estimated to be 81–113 μmol kg−1 and 12.7–15.7 μmol kg−1, respectively, in the Western Subarctic Gyre. The variability in nutrients between May and July was generally at least double that in other seasons. In the Western Subarctic Gyre, estimations based on statistical analyses revealed that seasonal new production was 39–61 gC m−2 and tended to be higher in the southwestern regions or coastal regions. The seasonal new productions in the northwestern North Pacific were two or more times higher than in the North Pacific subtropical gyre and the northeastern North Pacific. It is likely that this difference is due to spatial variations in the concentrations of trace metals and the species of phytoplankton present. In addition, from estimations of surface pCO2 it was verified that the Western Subarctic Gyre is a source of atmospheric CO2 between February and May and a sink for CO2 between July and October.  相似文献   

4.
The importance of the North Pacific Intermediate Water as a sink for the anthropogenic carbon dioxide has been examined by mapping chemical and radiochemical properties at two isopycnal surfaces of of 26.6 ad 27.2 obtained in 1970's. Its radiocarbon contents in 1980's were determined for comparison. The isopleths of depth and salinity at the two isopycnal surfaces obviously show that the intermediate layer of the entire mid-latitudes of the North Pacific is occupied by a similar water mass. The distributions of dissolved oxygen contents and Si/N ratios in the intermediate water indicate its source in the northwestern North Pacific and its sink in the eastern Pacific. The 14C values clearly designate the intrusion of the artificial radiocarbon of mostly 1960's origin into the upper intermediate water of the western North Pacific having its maximum in the subarctic zone of 40–45°N and 160–180°E in 1973. The maximum region for tritium is much broader extending to the north. These suggest that the subboreal region is active in the gas exchange and/or the warm water residing for a long time at the surface and flowing into the region across the subarctic front sinks quickly in winter. At the lower isopycnal surface, the increase 14C value for 14±4 years was around 27, which is smaller than that expected from the total carbonate increase, indicating an active isopycnal mixing.  相似文献   

5.
Settling particles play an important role in transporting organic carbon from the surface to the deep ocean. It is known that major components of settling particles are biogenic silicates (opal), biogenic carbonate (CaCO3), lithogenic clays and organic matter. Since each component aggregates and/or takes in organic carbon, all of these components have the ability to transport particulate organic carbon (POC) to the interior of the ocean. In this study, sediment trap experiments were carried out in four areas of the western North Pacific (including a marginal sea). Factors are proposed that correlate the composition of settling particles with POC flux. Annual mean organic carbon fluxes at 1 km depth in the western North Pacific Basin, Japan Sea, Hidaka Basin and northern Japan Trench were found to be 14.9, 18.1, 13.0 and 6.6 mg/m2/day, respectively. Organic carbon flux in the western North Pacific was greater than that in the Eastern North Pacific (7.4), the Equatorial Pacific (4.2), the Southern Ocean (5.8) and the Eastern North Atlantic (1.8). In the western North Pacific, it was calculated that 52% of POC was carried by opal particles. Opal is known to be a major component even in the Eastern North Pacific and the Southern Ocean, and the opal fluxes in these areas are similar to those in the western North Pacific. However, the organic carbon flux that was carried by opal particles (OCopalflux) in the western North Pacific was greater than that in the Eastern North Pacific and the Southern Ocean. These results indicate that the ability of opal particles to transport POC to the deep ocean in the western North Pacific is greater than that in the other areas.  相似文献   

6.
A global ocean inverse model that includes the 3D ocean circulation as well as the production, sinking and remineralization of biogenic particulate matter is used to estimate the carbon export flux in the Pacific, north of 10°S. The model exploits the existing large datasets for hydrographic parameters, dissolved oxygen, nutrients and carbon, and determines optimal export production rates by fitting the model to the observed water column distributions by means of the “adjoint method”. In the model, the observations can be explained satisfactorily with an integrated carbon export production of about 3 Gt C yr−1 (equivalent to 3⋅1015 gC yr−1) for the considered zone of the Pacific Ocean. This amounts to about a third of the global ocean carbon export of 9.6 Gt C yr−1 in the model. The highest export fluxes occur in the coastal upwelling region off northwestern America and in the tropical eastern Pacific. Due to the large surface area, the open-ocean, oligotrophic region in the central North Pacific also contributes significantly to the total North Pacific export flux (0.45 Gt C yr−1), despite the rather small average flux densities in this region (13 gC m−2yr−1). Model e-ratios (calculated here as ratios of model export production to primary production, as inferred from satellite observations) range from as high a value as 0.4 in the tropical Pacific to 0.17 in the oligotrophic central north Pacific. Model e-ratios in the northeastern Pacific upwelling regions amount to about 0.3 and are lower than previous estimates. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

7.
A preliminary study of carbon system in the East China Sea   总被引：1，自引：0，他引：1  
In the central part of the East China Sea, the activity of CO2 in the surface water and total carbonate, pH and alkalinity in the water column were determined in winter and autumn of 1993. The activity of CO2 in the continental shelf water was about 50 ppm lower than that of surface air. This decrease corresponds to the absorption of about 40 gC/m2/yr of atmospheric CO2 in the coastal zone or 1 GtC/yr in the global continental shelf, if this rate is applicable to entire coastal seas. The normalized total carbonate contents were higher in the water near the coast and near the bottom. This increase toward the bottom may be due to the organic matter deposited on the bottom. This conclusion is supported by the distribution of pH. The normalized alkalinity distribution also showed higher values in the near-coast water, but in the surface water, indicating the supply of bicarbonate from river water. The residence time of the East China Sea water, including the Yellow Sea water, has been calculated to be about 0.8 yr from the excess alkalinity and the alkalinity input. Using this residence time and the excess carbonate, we can estimate that the amount of dissolved carbonate transported from the coastal zone to the oceanic basin is about 70 gC/m2/yr or 2 GtC/yr/area-of-global-continental-shelf. This also means that the rivers transport carbon to the oceans at a rate of 30 gC/m2/yr of the coastal sea or 0.8 GtC/yr/ area-of-global shelf, the carbon consisting of dissolved inorganic carbonate and terrestrial organic carbon decomposed on the continental shelf.  相似文献   

8.
The fluorescence of dissolved organic matter in seawater   总被引：3，自引：0，他引：3  
A total of 28 vertical profiles of seawater fluorescence was measured in the Sargasso Sea, the Straits of Florida, the Southern California Borderlands, and the central Pacific Ocean. In all cases, surface seawater fluorescence was low as a result of photochemical bleaching which occurs on the timescale of hours. Fluorescence of deep water was 2–2.5 times higher than that of surface waters, and was constant, implying a long residence time for fluorescent organic matter, possibly of the order of thousands of years. Fluorescence correlates well with nutrients (NO3−, PO43−) in mid-depth waters (100–1000 m) in the Sargasso Sea and the central North Pacific, consistent with results in the central Pacific and the coastal seas of Japan. This suggests that regeneration or formation of fluorescent materials accompanies the oxidation and remineralization of settling organic particles.The various sources and sinks of fluorescent organic matter in the global oceans are assessed. The major sources are particles and in situ formation; rivers, rain, diffusion from sediments, and release from organisms are minor sources. The major sink is photochemical bleaching.  相似文献   

9.
The Fukushima nuclear accident in 2011 released large amounts of radionuclides, including ~(137)Cs, into the Pacific Ocean. A quasi-global ocean radioactive transport model with horizontal grid spacing of 0.5°×0.5° and 21 vertical layers was thereafter established to study the long-term transport of the Fukushima-derived ~(137)Cs in the ocean.The simulation shows that the plume of ~(137)Cs would be rapidly transported eastward alongside the Kuroshio Current and its extensions. Contaminated waters with concentrations lower than 2 Bq/m3 would reach the west coast of North America 4 or 5 years after the accident. The ~(137)Cs tends to be carried, despite its very low concentration, into the Indian and South Pacific Oceans by 2016 via various branches of ocean currents.Meanwhile, the ~(137)Cs concentrations in the western part of the North Pacific Ocean decrease rapidly with time. Up to now the highly contaminated waters have remained in the upper 400 m, showing no evidence of significant penetration to deeper layers.  相似文献   

10.
The depth of penetration of anthropogenic CO2 in the North Pacific Ocean based on carbonate data in the literature is discussed. The results indicate that the deepest penetration (over 2000 m) is found in the northwest North Pacific. The shallowest penetration (to less than 400 m) is found in the eastern equatorial Pacific. Depth of penetration of anthropogenic CO2 appears to have been controlled by such factors as deep water formation in the Northwest Pacific; upwelling in the equatorial Pacific and; vertical mixing in the western boundary areas. These results compare well with results implied from tritium, C-14, and freons distributions. The total inventory of excess carbon in the North Pacific was 14.7±4×1015 g around 1980.  相似文献   

11.
Meridional ocean freshwater transports and convergences are calculated from absolute geostrophic velocities and Ekman transports. The freshwater transports are analyzed in terms of mass-balanced contributions from the shallow, ventilated circulation of the subtropical gyres, intermediate and deep water overturns, and Indonesian Throughflow and Bering Strait components. The following are the major conclusions:
1.
Excess freshwater in high latitudes must be transported to the evaporative lower latitudes, as is well known. The calculations here show that the northern hemisphere transports most of its high latitude freshwater equatorward through North Atlantic Deep Water (NADW) formation (as in [Rahmstorf, S., 1996. On the freshwater forcing and transport of the Atlantic thermohaline circulation. Climate Dynamics 12, 799-811]), in which saline subtropical surface waters absorb the freshened Arctic and subpolar North Atlantic surface waters (0.45 ± 0.15 Sv for a 15 Sv overturn), plus a small contribution from the high latitude North Pacific through Bering Strait (0.06 ± 0.02 Sv). In the North Pacific, formation of 2.4 Sv of North Pacific Intermediate Water (NPIW) transports 0.07 ± 0.02 Sv of freshwater equatorward.In complete contrast, almost all of the 0.61 ± 0.13 Sv of freshwater gained in the Southern Ocean is transported equatorward in the upper ocean, in roughly equal magnitudes of about 0.2 Sv each in the three subtropical gyres, with a smaller contribution of <0.1 Sv from the Indonesian Throughflow loop through the Southern Ocean. The large Southern Ocean deep water formation (27 Sv) exports almost no freshwater (0.01 ± 0.03 Sv) or actually imports freshwater if deep overturns in each ocean are considered separately (−0.06 ± 0.04 Sv).This northern-southern hemisphere asymmetry is likely a consequence of the “Drake Passage” effect, which limits the southward transport of warm, saline surface waters into the Antarctic [Toggweiler, J.R., Samuels, B., 1995a. Effect of Drake Passage on the global thermohaline circulation. Deep-Sea Research I 42(4), 477-500]. The salinity contrast between the deep Atlantic, Pacific and Indian source waters and the denser new Antarctic waters is limited by their small temperature contrast, resulting in small freshwater transports. No such constraint applies to NADW formation, which draws on warm, saline subtropical surface waters .
2.
The Atlantic/Arctic and Indian Oceans are net evaporative basins, hence import freshwater via ocean circulation. For the Atlantic/Arctic north of 32°S, freshwater import (0.28 ± 0.04 Sv) comes from the Pacific through Bering Strait (0.06 ± 0.02 Sv), from the Southern Ocean via the shallow gyre circulation (0.20 ± 0.02 Sv), and from three nearly canceling conversions to the NADW layer (0.02 ± 0.02 Sv): from saline Benguela Current surface water (−0.05 ± 0.01 Sv), fresh AAIW (0.06 ± 0.01 Sv) and fresh AABW/LCDW (0.01 ± 0.01 Sv). Thus, the NADW freshwater balance is nearly closed within the Atlantic/Arctic Ocean and the freshwater transport associated with export of NADW to the Southern Ocean is only a small component of the Atlantic freshwater budget.For the Indian Ocean north of 32°S, import of the required 0.37 ± 0.10 Sv of freshwater comes from the Pacific through the Indonesian Throughflow (0.23 ± 0.05 Sv) and the Southern Ocean via the shallow gyre circulation (0.18 ± 0.02 Sv), with a small export southward due to freshening of bottom waters as they upwell into deep and intermediate waters (−0.04 ± 0.03 Sv).The Pacific north of 28°S is essentially neutral with respect to freshwater, −0.04 ± 0.09 Sv. This is the nearly balancing sum of export to the Atlantic through Bering Strait (−0.07 ± 0.02 Sv), export to the Indian through the Indonesian Throughflow (−0.17 ± 0.05 Sv), a negligible export due to freshening of upwelled bottom waters (−0.03 ± 0.03 Sv), and import of 0.23 ± 0.04 Sv from the Southern Ocean via the shallow gyre circulation.
3.
Bering Strait’ssmall freshwater transport of <0.1 Sv helps maintains the Atlantic-Pacific salinity difference. However, proportionally large variations in the small Bering Strait transport would only marginally impact NADW salinity, whose freshening relative to saline surface water is mainly due to air-sea/runoff fluxes in the subpolar North Atlantic and Arctic. In contrast, in the Pacific, because the total overturning rate is much smaller than in the Atlantic, Bering Strait freshwater export has proportionally much greater impact on North Pacific salinity balances, including NPIW salinity.
  相似文献   

12.
Radiocarbon and total carbonate data were obtained near the 1973 GEOSECS stations in the North Pacific along 30°N and along 175°E between 1993 and 1994. In these stations, we estimated radiocarbon originating from atomic bomb tests using tritium, trichlorofluoromethane and silicate contents. The average penetration depth of bomb radiocarbon during the two decades has deepened from 900 m to 1300 m. Bomb radiocarbon inventories above the average value for the whole North Pacific were found widely in the western subtropical region around 30°N both in the 1970s and 1990s, and its area in the 1990s was broader than that in the 1970s. In most of the North Pacific, while the bomb radiocarbon has decreased above 25.4, the bomb radiocarbon flux below 25.4 was over 1 × 1012 atom m-2yr-1 in the subtropical region around 30°N. In the tropical area south of 20°N, the bomb radiocarbon inventory below 25.4 increased from zero to over 10 × 1012 atom m-2 during the last three decades. These distributions suggest that the bomb radiocarbon removed from the surface is currently accumulated with bomb 14C flux of over 1 × 1012 atom m-2yr-1 below 25.4 in the subtropical region, mainly by advection from the higher latitude, and that part of the accumulated bomb 14C gradually spread southward with about 30 years.  相似文献   

13.
An array of five bottom-tethered moorings with 19 PARFLUX time-series sediment trap at three depths (1 and 2 km below the surface, and 0.7 km above the sea-floor) was deployed in the western Pacific sector of the Southern Ocean, along 170°W. The five stations were selected to sample settling particles in the main hydrological zones of the Southern Ocean. The sampling period spanned 425 days (November 28, 1996–January 23, 1998) and was divided into 13 or 21 synchronized time intervals. A total of 174 sequential samples were recovered and analyzed to estimate fluxes of total mass (TMF), organic carbon, carbonate, biogenic silica, and lithogenic particles. The fluxes of biogenic material were higher than anticipated, challenging the notion that the Southern Ocean is a low-productivity region. Organic carbon fluxes at 1 km depth within the Polar Frontal Zone and the Antarctic Zone were relatively uniform (1.7–2.3 g m−2 yr−1), and about twice the estimated ocean-wide average (ca. 1 g m−2 yr−1). Carbonate fluxes were also high and uniform between the Subantarctic Front and ca. 64°S (11–13 g m−2 yr−1). A large fraction of the carbonate flux in the Antarctic Zone was due to the presence of pteropod shells. Coccoliths were found only to the north of the Polar Front, and calcium carbonate became the dominant phase in the Subantarctic Zone. In contrast, carbonate particles were nearly absent near 64°S. Latitudinal variations in biogenic silica fluxes were substantial. The large opal flux (57 g m−2 yr−1) measured in the Antarctic Zone suggests that opal productivity in this region has been previously underestimated and helps to explain the high sedimentary opal accumulation often found south of the Polar Front. Unlike biogenic material, fluxes of lithogenic particles were among the lowest measured in the open-ocean (0.12–0.05 g m−2 yr−1), reflecting a very low dust input.  相似文献   

14.
通过对南海北部夏、冬两个季节的生源要素垂直输运剖面和时间系列沉积物捕获器的测量资料进行综合研究表明:南海北部颗粒物质主要是由钙质生物壳、生物硅、海洋浮游生物的有机质以及岩源物质组成,颗粒物质通量在1 000 m处大约为90.0 mg/(m2·d);研究还表明颗粒有机碳在进入沉积物保存之前被大量溶解,南海北部来自底层顺坡搬运的有机碳远大于垂直沉降;与开阔大洋(东太平洋海域)的对比研究表明,边缘海对于季节的变化更加敏感,而东太平洋调查区位于热带赤道高生产力带,生物作用十分明显,其海洋生物呼吸和物质转移同样也较活跃.  相似文献   

15.
More than 14,000 measurements of surface water xCO2 were obtained during two cruises, 3 weeks apart in June 2000, along 155°E between 34 and 44°N in the western North Pacific Ocean. Based on the distributions of salinity and sea surface temperature (SST), the region has been divided into 6 subregions; Oyashio, Oyashio front, Transition, Kuroshio front, and Kuroshio extension I and II zones, from north to south. The surface waters were always undersaturated with respect to atmospheric CO2. The Oyashio water was the least undersaturated: its xCO2 decreased slightly by 7 ppm, while SST increased by 2°C. The xCO2 normalized to a constant temperature decreased considerably. In the two frontal zones, a large drawdown of 30–40 ppm was observed after 18–19 days. In the Kuroshio extension zones, the xCO2 increased, but the normalized xCO2 decreased considerably. The Transition zone water may be somewhat affected by mixing with the subsurface water, as indicated by the smallest SST rise, an undecreased PO4 concentration, and a colder and less stable surface layer than the Oyashio front water. As the uncertainty derived from the air-sea CO2 flux was not large, the xCO2 data allowed us to calculate the net biological productivity. The productivities around 60 mmol C m−2d−1 outside the Transition zone indicate that the northwestern North Pacific, especially the two frontal zones, can be regarded as one of the most productive oceans in the world.  相似文献   

16.
Using objectively analyzed seasonal fields of dissolved oxygen content, percent oxygen saturation, and apparent oxygen utilization (AOU), we describe the large-scale seasonal variability of oxygen for the Atlantic and Pacific Oceans in the upper 400 m. The winter minus summer basin zonal averages of AOU reveal a two-layer feature in both the Atlantic and the Pacific, for both hemispheres. Biological activity and seasonal stratification in the summer give the upper 50–75 m of the water column in each basin a lower AOU in summer than winter. Greater mixing of upper ocean waters in winter gives the 75–400 m layer lower AOU values in that season. The basin integral seasonal volumes of oxygen for both the North Atlantic and the North Pacific mirror what is occurring in the atmosphere, indicating that there is a seasonal flux of oxygen across the air–sea interface. Winter total O2 volume in the ocean is above the annual mean; the summer volume is below. Larger seasonal differences in the total O2 content are observed in the North Atlantic Ocean than the North Pacific Ocean. A seasonal net outgassing (SNO) of 8.3×1014 moles O2 is calculated from basin means, which is 25% higher than previous results.  相似文献   

17.
A simple dissolved silica (Si) and dissolved oxygen (O) diagram method was applied to study the deep-water circulation in the North Pacific and the following results and conclusion have been obtained. In the abyssal water flowing northward in the western Pacific Si increases with a constant ratio of Si to decreasing O(Si/O=–0.30). The water is designated as the main sequence. In the eastern Pacific the Si-O diagram is characteristic of the location and reflects the degrees of mixing with older waters and of alteration due to decomposition of biogenic material. The Bay of Alaska is found to be a great source of silica in the North Pacific and its bottom water spreads out to the central North Pacific north of 40°N, called here the abyssal front. The younger abyssal water in the Aleutian Trench flowing to the eastern North Pacific north of 40°N comes through the north end of the Kuril-Kamchatka Trench instead of the gap in the Emperor Seamounts at about 46°N. The deep water is almost completely homogenized by active isopycnal mixing and advection when the deep water reaches its upper boundary by upwelling in the western North Pacific including the Bering Sea. Thus the high productivity in the Bering Sea is principally caused neither by the direct supply of abyssal water rich in nutrients nor by the extremely active vertical mixing reaching depths greater than 500 m, but it may be caused simply by the shallower upper boundary of the deep water mass in the Bering Sea, from which nutrients are easily transported to the surface.  相似文献   

18.
深海富稀土沉积物因其资源潜力巨大,近年来备受关注。一般认为,沉积物中稀土元素和钇（总称REY）的主要来源为上覆海水,但针对富稀土海区上覆海水中REY的研究较少。本研究针对南太平洋富稀土海区采集的3个站位的全水深海水样品,测试出了15种溶解态REY,并对比了邻近海域已发表的数据,分析了该海区REY的空间分布特征。研究区表层水中溶解态REY浓度主要受风尘输入影响,而中层和深层水体中溶解态REY浓度主要受水团控制。经过澳大利亚后太古代页岩（PAAS）和北太平洋深层水（NPDW）归一化后的配分模式可确定REY间的分馏特征,分辨出不同水团。与其他大洋中报道的REY数据比较发现,表层水中REY浓度受风尘和河流输入影响导致差别较大,中层水中REY浓度与印度洋较为接近,深层水中REY浓度与不同大洋的水团年龄表现为正相关趋势,即REY浓度由小到大依次为大西洋、印度洋、南太平洋、北太平洋。  相似文献   

19.
A column concentration-high resolution inductively coupled plasma mass spectrometry (ICP-MS) determination was applied to measure the total dissolved concentrations of Fe, Co, Ni, Cu and Zn in seawater collected from the subarctic North Pacific (~45°N) and the Bering Sea in July–September 1997. Total adsorbable Mn was determined on board by column electrolysis preconcentration and chemiluminescence detection. The vertical profiles for Fe, Ni and Zn were nutrient-like. The deep water concentration of Fe was ~0.5 nM in the northeast Pacific (18°-140°W) and increased to ~1 nM in the northwest Pacific (161°E) and ~2 nM in the Bering Sea (57°N, 180°E). The deep water concentrations for Ni and Zn in the Bering Sea were also 1.3–2 times higher than in the North Pacific. The profiles for Co and Cu were examined in the subarctic North Pacific, and results obtained were consistent with previous reports. There was a significant correlation between the concentrations of Co and Mn except for surface mixed layer. The profiles for total adsorbable Mn were similar to the reported profiles for total dissolvable Mn. The deep water concentration of Mn in the Bering Sea was also 4 times higher than in the North Pacific. Iron and zinc were depleted in surface water of the subarctic North Pacific. The relationship between these trace elements and nutrients suggests that these elements could be a limiting factor of phytoplankton productivity. In the Bering Sea, surface water contained ~0.3 nM of Fe. The Zn concentration, which was less than the detection limit in surface water, increased at shallower depths (~30 m) compared with the subarctic North Pacific. These results imply a higher flux of Fe and Zn to surface water in the Bering Sea. This in turn may cause the ecosystem in the Bering Sea characterized by a dominance of diatoms and high regenerated production.  相似文献   

20.
Fifty years of measurements at Ocean Station Papa (OSP, 50°N, 145°W) show trends in the interior waters of the subarctic Pacific that are both impacted by short term (few years to bi-decadal) atmospheric or ocean circulation oscillations and by persistent climate trends. Between 1956 and 2006, waters below the ocean mixed layer to a depth of at least 1000 m have been warming and losing oxygen. On density surfaces found in the depth range 100-400 m (σθ = 26.3-27.0), the ocean is warming at 0.005-0.012 °C y−1, whereas oxygen is declining at 0.39-0.70 μmol kg−1 y−1 or at an integrated rate of 123 mmol m−2 y−1 (decrease of 22% over 50 years). During this time, the hypoxic boundary (defined as 60 μmol O2 kg−1) has shoaled from ∼400 to 300 m. In the Alaska Gyre, the 26.2 isopycnal occasionally ventilates, whereas at OSP 26.0σθ has not been seen at the ocean surface since 1971 as the upper ocean continues to stratify. To interpret the 50 year record at OSP, the isopycnal transport of oxygenated waters within the interior of the subarctic Pacific is assessed by using a slightly modified “NO” parameter [Broecker, W., 1974. “NO” a conservative water-mass tracer. Earth and Planetary Science Letters 23, 100-107]. The highest nitrate-oxygen signature in interior waters of the North Pacific is found in the Bering Sea Gyre, Western Subarctic Gyre and East Kamchatka Current region as a consequence of winter mixing to the ∼26.6 isopycnal. By mixing with low NO waters found in the subtropics and Okhotsk Sea, this signature is diluted as waters flow eastward across the Pacific. Evidence of low NO waters flowing north from California is seen along the coasts of British Columbia and SE Alaska. Oxygen in the subsurface waters of the Alaskan Gyre was supplied ∼60% by subarctic and 40% by subtropical waters during WOCE surveys, whereas such estimates are shown to periodically vary by 20% at OSP. Other features discernable in the OSP data include periods of increased ventilation of deeper isopycnals on an ∼18 year cycle and strong, short term (few month) variability caused by passing mesoscale eddies. The potential impacts of declining oxygen on coastal ecosystems are discussed.  相似文献   

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