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1.
Dissolved trace element distributions near Elephant Island in the Drake Passage show extremely high levels of dissolved Fe and Mn in waters above the shelf. The entrainment of this enriched shelf water by the Fe-poor Antarctic Circumpolar Current (ACC) as it passes through the Shackleton Gap delivers an estimated 2.8×106 mol yr−1 dissolved Fe to the offshore waters of the Drake Passage. The magnitude and spatial distribution of dissolved Fe, Mn and Al over the shelf are consistent with a diagenetically produced sedimentary source, but are inconsistent with eolian or upwelling sources. The systematics of the Mn and Fe concentrations suggest that there are two distinct sources of dissolved Fe to the surface waters of this region. The highest Fe concentrations are associated with Bransfield Strait water, which can be identified by its characteristic temperature and salinity (T/S) properties both inside the Bransfield Strait and in the Bransfield Current outflow between Elephant and Clarence Islands. Most of the shelf area is dominated by a second water type with T/S properties that are typical of modified Antarctic Surface Water, which while also enriched has a lower Fe:Mn ratio.The predominantly linear relationships between the Fe and Mn concentrations at the stations in each of these water mass types suggest that the distribution of these elements is largely controlled by physical mixing processes and that biological removal of Fe on the shelf, while certainly occurring, is limited, perhaps as a result of rapid physical flushing processes and relatively slow biological growth rates. The consequent export of large quantities of this shelf-derived Fe into the ACC is likely responsible for the extensive regions of enhanced primary production seen in satellite imagery downstream of the Drake Passage.  相似文献   

2.
Based on the long-term surveys in 1995?C2010, the influence of the variability of the winter conditions on the interannual dynamics of the content of dissolved oxygen was studied concerning the deep waters (the 40 m isobath line) of the eastern part of the Gulf of Finland. The content of oxygen varied within a wide range with a low-pronounced trend to a decrease during the considered period. All the processes affecting the aeration of deep waters, i.e., the advection of oxygen-depleted saline waters from the Baltic Sea and the intensity of the autumnal and winter mixing, correlated with the North Atlantic oscillation index, which determined the close positive correlation between this parameter and the oxygen content (r = +0.87). The hypoxic effects in the gulf were registered in the years of negative anomalies of the North Atlantic oscillation. The conclusion is reached that the deterioration of the oxygen conditions at the inner part of the Gulf of Finland during the late 20th-early 21st century is mainly caused by the large-scale variations in the atmospheric processes.  相似文献   

3.
Based on measurements of the 18O isotope composition of 247 samples collected over a 3-year period we have assessed the oxygen isotope composition of water masses in the North Sea. This is the first δ18O data set that covers the entire North Sea basin. The waters lie on a mixing line: δ18O (‰VSMOW) = −9.300 + 0.274(S) with North Atlantic sub-polar mode water (SPMW) and surface waters, and Baltic Sea water representing the saline and freshwater end members respectively. Patterns exhibited in surface and bottom water δ18O distributions are representative of the general circulation of the North Sea. Oxygen-18 enriched waters from the North Atlantic enter the North Sea between Scotland and Norway and to a lesser extent through the English Channel. In contrast, oxygen-18 depleted waters mainly inflow from the Baltic Sea, the rivers Rhine and Elbe, and to a lesser degree, the Norwegian Fjords and other river sources. Locally the δ18O–salinity relationship will be controlled by the isotopic composition of the freshwater inputs. However, the range of local freshwater compositions around the North Sea basin is too narrow to characterise the relative contributions of individual sources to the overall seawater composition. This dataset provides important information for a number of related disciplines including biogeochemical research and oceanographic studies.  相似文献   

4.
Suspended matter was collected at 30 stations in the Baltic and Kattegatt, at the thermocline and at the bottom, and analysed for Na, Ca, Mg, Si, Ti, Al, Fe, Mn, Ba, Sr, Ni and V. The composition of the suspended matter varies considerably, but can be described as a mixture of: (1) 12–25% terrigenous detritus with much Si, Al, Ti and Fe; (2) 75–88% biological matter with much Ni, V and Ba; and (3) some Mn-oxyhydroxide.The annual efflux of water from the Baltic is about 460 km3, with a suspended load in the Baltic straits of ～1.2–3.6 mg ash material l?1 These values imply that much Si, Ti, Al, Fe, Sr, Ni and V and particularly much Ba and Mn are lost from the Baltic in the suspended load.The average suspended matter is richer in Mn(5×), Ba(2.5×), Sr(4×) and V(1.8×) than permanently depositing Baltic sediments. These constituents are relatively enriched in pelagic deposits, i.e. it is likely that much Mn, Ba and V in deep-sea sediments derive from the continents via suspended transport. This conclusion is supported by the similarity between suspended matter and average Atlantic pelagic sediment.  相似文献   

5.
In the framework of the German contribution to the Joint Global Ocean Flux Study (JGOFS), deep-water fluxes of particle-associated trace elements were measured in the northeast Atlantic Ocean. The sinking particles were collected almost continuously from 1992 to 1996 at three time-series stations, L1 (33°N/22°W), L2 (47°N/20°W), and L3 (54°N/21°W), using sediment traps. The focus of the present study is the temporal variability of the particle-associated elemental fluxes of Al, Ca, Cd, Co, Cu, Fe, Mn, Ni, P, Pb, Ti, V, and Zn at a depth of 2000 m.A clear seasonality of the fluxes that persisted for several years was documented for the southernmost station (L1) at stable oligotrophic conditions in the area of the North Atlantic Subtropical Gyre East (NASTE). At L2 and L3, an episodic nature of the elemental fluxes was determined. Mesoscale eddies are known to frequently cause temporal and spatial variability in the flux of biogenic components in that area. These events modified the simple seasonal pattern controlled by the annual cycle at L2, in the North Atlantic Drift Region (NADR), and at L3, which was influenced by the Atlantic Arctic province (ARCT). All stations were characterized by an additional episodic lithogenic atmospheric supply reaching the deep sea.The integrated annual fluxes during the multi-year study revealed similar flux magnitudes for lithogenic elements (Al, Co, Fe, Ti, and V) at L2 and L3 and roughly twofold fluxes at L1. Biogenic elements (Cd, P, and Zn) showed the opposite trend, i.e., two to fourfold higher values at L2 and L3 than at L1. For Mn, Ni, and Cu, the spatial differences were smaller, perhaps because of the intermediate behavior, between lithogenic and biogenic, of these elements. Similarly, among the three study sites, there were no noticeable differences in the total annual flux of Pb.The respective lithogenic fractions of the deep-sea fluxes of Cd, Co, Cu, Mn, Ni, V, and Zn were subtracted based on the amount of Al, with the average composition of the continental crust as reference. This procedure allowed estimation of the labile trace element fraction (TEexc) of the particles, i.e., TE taken up or scavenged during particle production and sedimentation. The ratios of TEexc/P clearly demonstrated an enrichment of TE over labile P from biogenic surface material to the deep sea for Zn (factor 4–6), Mn (12–27), Ni (3–5), and Cu (9–25); an intermediate status for Co (0.5–2.2); and depletion for Cd vs. P (0.2–0.4). Surprisingly, the recycling behavior of excess Co was found to be similar to that of P. Hence, Coexc behaved like a biogenic element; this is in contrast to total Co, which is dominated by the refractory lithogenic fraction.Moreover, it is argued that these excess elemental fluxes caused a loss of the dissolved elements in upper waters, since their transport reaches the deep-sea waters at 2000 m, a depth far below of deep-winter mixing and upwelling. The annual amount of excess TE exported from surface waters was estimated to be 1.3×109 mol Zn y?1, 4.4×109 mol Mn y?1, 4.9×108 mol Ni y?1, 2.2×107 mol Cd y?1, 7.4×108 mol Cu y?1, and 2.7×107 mol Co y?1 for the whole North Atlantic Ocean. Important primary sources that could replenish these losses are the aeolian and fluvial supply processes.  相似文献   

6.
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   

7.
The ratio of oxygen-18 to oxygen-16 (expressed as per mille deviations from Vienna Standard Mean Ocean Water, δ18O) is reported for seawater samples collected from seven full-depth CTD casts in the northern North Atlantic between 20° and 41°W, 52° and 60°N. Water masses in the study region are distinguished by their δ18O composition, as are the processes involved in their formation. The isotopically heaviest surface waters occur in the eastern region where values of δ18O and salinity (S) lie on an evaporation–precipitation line with slope of 0.6 in δ18O–S space. Surface isotopic values become progressively lighter to the west of the region due to the addition of 18O-depleted precipitation. This appears to be mainly the meteoric water outflow from the Arctic rather than local precipitation. Surface samples near the southwest of the survey area (close to the Charlie Gibbs Fracture Zone) show a deviation in δ18O–S space from the precipitation mixing line due to the influence of sea ice meltwater. We speculate that this is the effect of the sea ice meltwater efflux from the Labrador Sea. Subpolar Mode Water (SPMW) is modified en route to the Labrador Sea where it forms Labrador Sea Water (LSW). LSW lies to the right (saline) side of the precipitation mixing line, indicating that there is a positive net sea ice formation from its source waters. We estimate that a sea ice deficit of ≈250 km3 is incorporated annually into LSW. This ice forms further north from the Labrador Sea, but its effect is transferred to the Labrador Sea via, e.g. the East Greenland Current. East Greenland Current waters are relatively fresh due to dilution with a large amount of meteoric water, but also contain waters that have had a significant amount of sea ice formed from them. The Northeast Atlantic Deep Water (NEADW, δ18O=0.22‰) and Northwest Atlantic Bottom Waters (NWABW, δ18O=0.13‰) are isotopically distinct reflecting different formation and mixing processes. NEADW lies on the North Atlantic precipitation mixing line in δ18O–salinity space, whereas NWABW lies between NEADW and LSW on δ18O–salinity plots. The offset of NWABW relative to the North Atlantic precipitation mixing line is partially due to entrainment of LSW by the Denmark Strait overflow water during its overflow of the Denmark Strait sill. In the eastern basin, lower deep water (LDW, modified Antarctic bottom water) is identified as far north as 55°N. This LDW has δ18O of 0.13‰, making it quite distinct from NEADW. It is also warmer than NWABW, despite having a similar isotopic composition to this latter water mass.  相似文献   

8.
Oxy-anionic species of V, As, Se, Mo, Sb, Te and W were measured in solution and suspension in samples obtained during several cruises in the Dutch Wadden Sea, the offshore region of the Southern Bight (North Sea) and in the estuaries of the Rhine and Scheldt. Dissolved concentrations at salinities above 34·5 × 10?3 ( = 34·5%. S) agreed generally well with published open ocean values. It is suggested that Se speciation differs from the open ocean.In the Wadden Sea, concentrations of V, Se, Mo and Sb were linearly related to salinity (10–35 × 10?3). The good agreement between measured and extrapolated values at a salinity of 0·5 × 10?3 suggests conservative behaviour in the Rhine estuary (with residence time of freshwater in the order of a few days).Dissolved concentration vs. salinity plots in the Scheldt estuary (residence time 2–3 months) showed pronounced minima and maxima. These occurred in the low or medium salinity range for V, As and Sb. Linear behaviour was observed for Se and Mo (in some cases, relatively large differences between cruises were detected). Deviations from linearity in the plots are interpreted in terms of thermodynamic equilibrium conditions involving species with different solubilities (V), local input from land (As, Se, Sb, Te) and removal from solution (As), probably through coprecipitation with Fe(OH)3.In the offshore samples, the contributions of particulate forms to the total element concentrations were small (<15%). At higher SPM concentrations (about 30 mg dm?3), this percentage remained small for Se, Mo and Sb (<15%); it was substantial for V and As (25–50%).  相似文献   

9.
Dissolved and total dissolvable manganese concentrations have been measured at four stations in the western North Atlantic Ocean. Total dissolvable manganese concentrations are high in surface waters, decrease to uniformly low levels throughout the bulk of the water column, and increase in the bottom nepheloid layer. Dissolved Mn (Mnd) concentrations follow the total dissolvable concentrations throughout the surface and deep waters but do not increase in the near-bottom waters.Deep water concentrations of Mnd decrease from 30 ng l?1 in the Newfoundland Basin to 20 ng l?1 in the Sargasso Sea. This change and other features of the deep water distribution of dissolved manganese could be associated with the slow oxidation of Mn2+ to MnO2. There is also evidence at one station of scavenging of manganese from the dissolved phase in the near-bottom layer which may again be related to the kinetics of manganese oxidation.  相似文献   

10.
Hong Kong waters receive high nutrient loading from year-round sewage effluent and Pearl River discharge during the summer wet season. We assessed the role of physical processes in reducing eutrophication by calculating a eutrophication reduction index for four different hydrographical areas and four seasons. We used outdoor incubation experiments to assess the response of phytoplankton when physical (mixing and dilution) processes and mesozooplankton grazing were reduced. The primary regulator of phytoplankton growth in low nutrient eastern waters (reference site) shifted from nutrients in the wet season to increased vertical mixing in the dry season. In the highly flushed western waters and Victoria Harbour, the majority (>86?%) of the eutrophication impacts were reduced by strong hydrodynamic mixing (turbulence, vertical mixing, and flushing effects) all year. In southern waters, eutrophication effects were severe (chlorophyll a of up to ~73?μg?L?1) and was regulated by the ambient phosphate (PO4) concentration (~0.1?μM) during summer. In contrast, 62–96?% of the potential eutrophication impacts were reduced by physical processes during other seasons. Bioassays also revealed that the yield of chlorophyll from dissolved inorganic nitrogen (DIN) that was taken up by phytoplankton [1.1–3.3?g?Chl (mol?N)?1] was not significantly different in both N- and P-limited cases. In contrast, the uptake ratios of DIN:PO4 (26:1–105:1) and Chl:P ratios [42–150?g?Chl (mol?P)?1] in the P-limited cases were significantly (p?<?0.05, t test) higher than the N-limited cases [~16DIN:1P and 22–48?g?Chl (mol?P)?1]. The C:Chl ratios ranged from 32 to 87?g?g?1. These potential ranges in ratios need to be considered in future nutrient models.  相似文献   

11.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.  相似文献   

12.
The relation between the nitrate and phosphate concentrations in the Sea of Okhotsk and the bordering waters of the Pacific Ocean were studied. The surveys were carried out in the autumn, spring, and summer of 2001–2002. For the deepwater part of the sea, the relation [NO? 3] = ((14.88 ± 0.07) × [PO3? 4] ? 5.46 ± 0.17) was found. The coefficients in the equation given are statistically different from those in the similar equation for the Pacific waters: [NO? 3] = (16.05 ± 0.15) × [PO3? 4]-(7.23 ± 0.36). In the northern part of the sea; on the shelf; in the slope area; and, especially, in the deep waters of the TINRO Depression, the linear dependence between the phosphate and nitrate concentrations was distorted. This feature was described in terms of nitrate deficiency. The maximum values of this deficiency were found in the near-bottom waters. The principal processes that might cause the nitrate deficiency were considered: the difference in the oxidation rates of the nitrogen and phosphorus organic compounds, the matter transfer between the continent and the sea, the different efficiency of the biogenic burial of nitrogen and phosphorus in the bottom sediments, and the denitrification in the upper layer of the bottom sediments. It was shown that the most probable cause of the nitrate deficiency was the denitrification. The loss of inorganic nitrogen owing to the supply of the waters of the Sea of Okhotsk to the Pacific Ocean was estimated as ～2.5 × 1011 mol N/year.  相似文献   

13.
The Arctic Ocean is connected to the Pacific by the Bering Sea and the Bering Strait. During the 4th Chinese National Arctic Research Expedition, measurements of carbon tetrachloride (CCl4) were used to estimate ventilation time-scales and anthropogenic CO2 (Cant) concentrations in the Arctic Ocean and Bering Sea based on the transit time distribution method. The profile distribution showed that there was a high-CCl4 tongue entering through the Canada Basin in the intermediate layer (27.6?<?σθ?<?28), at latitudes between 78 and 85°N, which may be related to the inflow of Atlantic water. Between stations B09 and B10, upwelling appeared to occur near the continental slope in the Bering Sea. The ventilation time scales (mean ages) for deep and bottom water in the Arctic Ocean (~?230–380 years) were shorter than in the Bering Sea (~?430–970 years). Higher mean ages show that ventilation processes are weaker in the intermediate water of the Bering Sea than in the Arctic Ocean. The mean Cant column inventory in the upper 4000 m was higher (60–82 mol m?2) in the Arctic Ocean compared to the Bering Sea (35–48 mol m?2).  相似文献   

14.
This study quantifies diapycnal mixing and vertical heat transfer in the Pacific side of the Arctic Ocean, where sea-ice cover has disappeared between July and September in the last few decades. We conducted microstructure measurements in the open water region around the Canada Basin from late summer to fall in 2009 and 2010 using R/V Mirai. In the study domain, the dissipation rate of turbulent kinetic energy, ε, is typically as low level as O(10?10) W kg?1, resulting in vertical heat diffusivity of O(10?7) m2 s?1, which is close to the molecular diffusivity of heat, suggesting comparatively little predominance of mechanical turbulent mixing. An exception is the case at the Barrow Canyon, where the strong baroclinic throughflow generates substantial vertical mixing, producing ε > O(10?7) W kg?1, because of the shear flow instability. Meanwhile, in the confluence region, where the warm/salty Pacific water and the cold/fresh Arctic basin water encounter, the micro-temperature profiles revealed a localized enhancement in vertical diffusivity of heat, reaching O(10?5) m2 s?1 or greater. In this region, an intrusion of warm Pacific water creates a horizontally interleaved structure, where the double-diffusive mixing facilitates vertical heat transfer between the intruding Pacific water and the surrounding basin waters.  相似文献   

15.
Atmospheric iron and underway sea-surface dissolved (<0.2 μm) iron (DFe) concentrations were investigated along a north–south transect in the eastern Atlantic Ocean (27°N/16°W–19°S/5°E). Fe concentrations in aerosols and dry deposition fluxes of soluble Fe were at least two orders of magnitude higher in the Saharan dust plume than at the equator or at the extreme south of the transect. A weaker source of atmospheric Fe was also observed in the South Atlantic, possibly originating in southern Africa via the north-easterly outflow of the Angolan plume. Estimations of total atmospheric deposition fluxes (dry plus wet) of soluble Fe suggested that wet deposition dominated in the intertropical convergence zone, due to the very high amount of precipitation and to the fact that a substantial part of Fe was delivered in dissolved form. On the other hand, dry deposition dominated in the other regions of the transect (73–97%), where rainfall rates were much lower. Underway sea-surface DFe concentrations ranged 0.02–1.1 nM. Such low values (0.02 nM) are reported for the first time in the Atlantic Ocean and may be (co)-limiting for primary production. A significant correlation (Spearman's rho=0.862, p<0.01) was observed between mean DFe concentrations and total atmospheric deposition fluxes, confirming the importance of atmospheric deposition on the iron cycle in the Atlantic. Residence time of DFe in the surface waters relative to atmospheric inputs were estimated in the northern part of our study area (17±8 to 28±16 d). These values confirmed the rapid removal of Fe from the surface waters, possibly by colloidal aggregation.  相似文献   

16.
The MnO2 adsorption method combined with voltammetry is proposed for the direct determination of metal complexation in seawater of various salinities as a more satisfactory alternative to direct voltammetric measurements and bioassay methods. A small quantity of MnO2 is equilibrated with copper ions in filtered seawater. Natural organic ligands in the seawater compete for copper with the MnO2. Total dissolved copper is measured by differential pulse anodic stripping voltammetry after filtration and acidification of the sample. Preconcentration of natural water samples is unnecessary and measurement is performed at the natural equilibrium pH of the aerated sample. The analytical limit of detection of the method depends on contamination from the filtration step, and for copper complexation a ligand concentration of 5 × 10?8 M was obtained. The sensitivity can be increased by use of radioisotopes as tracers. The method is very versatile in that complexation of various metals may be determined by any analytical method that measures total dissolved metal concentrations. Neither organic ligands nor their complexes with copper adsorb on the MnO2 at pH8, but at pH 1.8 MnO2 is an efficient scavenger for electroactive organic material.Samples of surface water from the Irish Sea and the Atlantic Ocean were found to contain ligand concentrations of 1.7 × 10?7 and 1.1 × 10?7 M, with conditional stability constants (log values) of 9.84 ± 0.13 and 9.86 ± 0.23, respectively, at pH 8.0.  相似文献   

17.
Here we report the first optical, sensor-based profiles of nitrate from the central Makarov and Amundsen and southern Canada Basins of the Arctic Ocean. These profiles were obtained as part of the International Polar Year program during spring 2007 and 2008 field seasons of the North Pole Environmental Observatory (NPEO) and Beaufort Gyre Exploration Program (BGEP). These nitrate data were combined with in-situ, sensor-based profiles of dissolved oxygen to derive the first high-resolution vertical NO profiles to be reported for the Arctic Ocean. The focus of this paper is on the halocline layer that insulates sea ice from Atlantic water heat and is an important source of nutrients for marine ecosystems within and downstream of the Arctic. Previous reports based on bottle data have identified a distinct lower halocline layer associated with an NO minimum at about S=34.2 that was proposed to be formed initially in the Nansen Basin and then advected downstream. Greater resolution afforded by our data reveal an even more pronounced NO minimum within the upper, cold halocline of the Makarov Basin. Thus a distinct lower salinity source ventilated the Makarov and not the Amundsen Basin. In addition, a larger Eurasian River water influence overlies this halocline source in the Makarov. Observations in the southern Canada Basin corroborate previous studies confirming multiple lower halocline influences including diapycnal mixing between Pacific winter waters and Atlantic-derived lower halocline waters, ventilation via brine formation induced in persistent openings in the ice, and cold, O2-rich lower halocline waters originating in the Eurasian Basin. These findings demonstrate that continuous sensing of chemical properties promises to significantly advance understanding of the maintenance and circulation of the halocline.  相似文献   

18.
Stoichiometry among bioactive trace metals in the Chukchi and Beaufort Seas   总被引：1，自引：1，他引：0  
The distribution of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb in seawater was investigated in the Chukchi and Beaufort Seas of the western Arctic Ocean in September 2000. The unfiltered and filtered seawater samples were used for determination of total dissolvable metal (TDM) and dissolved metal (DM), respectively. The concentration of labile particulate metal (LPM) was estimated with the difference between that of TDM and DM. The concentrations of TDAl, TDMn, TDFe, TDCo and TDPb varied substantially in the study area. The high concentrations occurred at stations near the Bering Strait, in the Mackenzie delta, and above reductive sediments on the shelf and slope. These elements were mostly dominated by labile particulate species, such as Fe?CMn oxides and species adsorbed on terrestrial clay. DCo was correlated with DMn over the study area (r?=?0.78, n?=?135), and the slope of the regression line was 27 times higher at a pelagic station than at a shelf station. TDNi, TDCu, TDZn and TDCd showed relatively small variations and were generally dominated by dissolved species. There was a moderate correlation between DCd and phosphate for all samples (r?=?0.79), whereas there were no significant correlation between the other DMs and nutrients. TDNi and TDCu showed a remarkable linearity for most stations except those near the Bering Strait (R 2?=?0.95, n?=?126). These results suggest that biogeochemical cycling including uptake by phytoplankton and remineralization from settling particles has only minor control over the distribution of trace metals in this area. Using the present data, the annual input of bioactive trace metals form the Bering Strait and the Mackenzie River was estimated. Also, the trace metal compositions of major water masses were evaluated. The dissolved elemental ratio was P:Al:Mn:Fe:Co:Ni:Cu:Zn:Cd?=?1:1.2?×?10?2:4.4?×?10?4:1.4?×?10?3:3.7?×?10?5:3.7?×?10?3:1.4?×?10?3:4.5?×?10?3:2.2?×?10?4 for Canada Basin deep water (CBDW). This ratio was significantly different from that for Pacific deep water and Bering Sea water, suggesting substantial modification of the trace metal compositions of seawater in the study area.  相似文献   

19.
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20.
Human encroachment on the coastal zone has led to concern about the impact of anthropogenic nitrogen (N) on estuarine and continental shelf waters. Western North Atlantic watershed budgets suggest that the export of human-derived N from estuaries to shelf waters off the east coast of the US may be significant; however, models based on water inputs and estimates of upwelling of deepwater nutrients to surface waters of the mid-Atlantic bight indicate that estuarine N may be a relatively minor component of the overall shelf N budget. Stable N isotope ratios could provide a means to assess the relative input of anthropogenic N to shelf waters, particularly since dissolved N from human sources has elevated δ15N values (range: 7–30‰). We collected particulate material from surface shelf waters off the US east coast from 2000 to 2005 at near-shore sample sites proximal to the mouth of six estuaries and corresponding sites farther offshore. Near-shore (mean 33.7 km from estuary mouth) δ15N values ranged from 5.5 to 7.7‰ Offshore values (mean 92.4 km from estuary mouth) were consistently lower than near-shore sites (average 4.7 ± 1.0‰ versus 6.8 ± 1.1‰), suggesting different N sources to near and offshore stations. Near-shore regions are often more productive, as mean monthly chlorophyll-a concentrations from the sea-viewing wide field-of-view sensor (SeaWiFS) were significantly higher at near-shore sites near the mouth of three of the six estuaries. A mass balance using a concentration-dependent mixing model with chlorophyll-a concentrations as a surrogate for dissolved inorganic nitrogen can account for all of the nitrogen at near-shore sites south of Cape Cod with estuarine nitrogen estimated to contribute 45–85% of the nitrogen to the near-shore surface particulate material. Our results support the hypothesis that estuarine nitrogen is influencing continental shelf ecosystems, and also provide preliminary evidence of the spatial extent of its influence on shelf waters in the mid-Atlantic bight.  相似文献   

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