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1.
The magnitude of the exchange flux at the water–sediment interface was determined on the basis of the ammonia concentration gradient at the near-bottom water–interstitial interface and Fick's first law. It was established that in Puck Bay, ammonia almost always passes from the sediment to water. Ammonia flux varied from 5 to 1434 μmol NH4-N m−2 day−1. In total,c. 138·2 tonneammonia year−1pass from sediments of Internal Puck Bay to near-bottom water, the equivalent value for External Puck Bay being 686·9 tonne year−1. In total, about 825 tonne ammonia year−1passes from the sediment to near-bottom water of Puck Bay. In interstitial waters, ammonia occurred in concentrations varying over a wide range (3–1084 μmol NH4-N dm−3).The basic factors affecting the magnitude of ammonia concentration in interstitial waters included: oxidation of organic matter, type of sediment, and inflow of fresh underground waters to the region examined.This paper involves preliminary studies only and constitutes a continuation of the studies on ionic macrocomponents and phosphorus in interstitial waters of Puck Bay undertaken previously.  相似文献   

2.
Macroalgae biomass and concentrations of nitrogen, phosphorus and chlorophyll a were determined weekly or biweekly in water and sediments, during the spring-summer of 1985 in a hypertrophic area of the lagoon of Venice. Remarkable biomass production (up to 286 g m−2 day−1, wet weight), was interrupted during three periods of anoxia, when macroalgal decomposition (rate: up to 1000 g m−2 day−1) released extraordinary amounts of nutrients. Depending on the macroalgae distribution in the water column, the nutrients released in water varied from 3·3 to 19·1 μg-at litre−1 for total inorganic nitrogen and from 1·8 to 2·7 μg-at litre−1 for reactive phosphorus. Most nutrients, however, accumulated in the surficial sediment (up to 0·640 and to 3·06 mg g−1 for P and N respectively) redoubling the amounts already stored under aerobic conditions, Phytoplankton, systematically below 5 mg m−3 as Chl. a, sharply increased up to 100 mg m−3 only after the release of nutrients in water by anaerobic macroalgal decomposition. During the algal growth periods, the N:P atomic ratio in water decreased to 0·7, suggesting that nitrogen is a growth-limiting factor. This ratio for surficial sediment was between 6·6 and 13·1, similar to that of macroalgae (8·6–12·0).  相似文献   

3.
Sediment samples were collected at stations along cross-shelf transects in Onslow Bay, North Carolina, during two cruises in 1984 and 1985. Station depths ranged from 11 to 285 m. Sediment chlorophyll a concentrations ranged from 0·06 to 1·87 μg g−1 sediment (mean, 0·55), or 2·6–62·0 mg m2. Areal sediment chlorophyll a exceeded water column chlorophyll a a at 16 of 17 stations, especially at inshore and mid-shelf stations. Sediment ATP concentrations ranged from 0 to 0·67 μg g−1 sediment (mean, 0·28). Values for both biomass indicators were lowest in the depth range including the shelf break (50–99 m). Organic carbon contents of the sediments were uniformly low across the shelf, averaging 0·159% by weight. Photography of the sediments revealed extensive patches of microalgae on the sediment surface.Our data suggest that viable benthic microalgae occur across the North Carolina continental shelf. The distribution of benthic macroflora on the North Carolina shelf indicates that sufficient light and nutrients are available to support primary production out to the shelf break. Frequent storm-induced perturbations do not favour settling of phytoplankton, an alternative explanation for the presence of microalgal pigments in the sediments. Therefore, we propose that a distinct, productive benthic microflora exists across the North Carolina continental shelf.  相似文献   

4.
Copper concentrations have been measured in more than 200 samples collected from an Alaskan fjord and continental shelf and slope regions in the northwestern Gulf of Alaska. Concentrations were lowest (2·1 nmol kg−1) at depths of 400–1000 m in the continental slope waters of the Gulf of Alaska. Copper increased systematically with decreasing salinities shoreward to concentrations >30 nmol kg−1 in fjord surface waters during summer months of high freshwater runoff. Copper concentrations increased with depth at an inner fjord station where deep basin waters have restricted circulation, and these data together with surface (<5 cm) pore water copper concentrations (mean=122 nmol kg−1) about an order of magnitude higher than bottom water copper concentrations are indicative of a flux of copper across the sediment-seawater interface. This latter was estimated at 32±12 nmol cm−2 annually, and represented less than 20% of the annual input to fjord surface water (228–411 nmol cm−2) added during summer months. Mass balances in bottom waters indicate a vigorous recycling of copper with a residence time estimated at 21±11 days. Most copper that is remobilized in surface sediments is returned to bottom waters and little (3%) is removed by subsequent diagenetic reaction in the buried sediments. However, an estimate of copper accumulating in anoxic fjord sediments was comparable with copper added to fjord surface waters suggesting that input-removal reactions rather than internal cycling controls copper geochemistry in this estuary.  相似文献   

5.
Fatty acids and hydrocarbons of sedimenting particles were investigated in the northeastern Adriatic Sea from November 1988 to December 1989. Particles were collected at approximately monthly intervals, using sediment traps deployed at 30 m depth (2 m above bottom). Seasonal changes in sedimentation of particulate matter were very pronounced. Hydrocarbon fluxes and concentrations were found to vary significantly depending on the season. They averaged 2.69 ± 1.44 mg m−2 day−1 and 232.4 ± 90.93 μg g−1 in winter, respectively. In late spring-early summer the corresponding values amounted to 0.045 ± 0.015 mg m−2 day−1 and 13.72 ± 5.56 μg g−1, and they increased towards autumn, when mean values of 0.517 ± 0.228 mg m−2 day−1 and 98.86 ± 48.72 μg g−1 were obtained. In contrast, fatty acid fluxes and concentrations were low during winter (0.26 ± 0.08 mg m−2 day−1 and 21.95 ± 3.35 μg g−1), increased slightly towards the summer (0.48 ± 0.12 mg m−2 day−1 and 139.9 ± 44.6 μ g−1) and reached maximum rate and concentration in autumn, when average values were 1.98 ± 1.30 mg m2 day−1 and 489.1 ± 186.7 μg g−1, respectively. The differences in composition, concentrations and fluxes of the fatty acids and hydrocarbons were related to the sources of sedimenting material, reflecting the influence of resuspension of bottom sediments during winter and the appearance of mucus aggregates during summer and their subsequent deposition in autumn.  相似文献   

6.
Concentrations of bacteria, chlorophyll a, and several dissolved organic compounds were determined during 11 tidal cycles throughout the year in a high and a low elevation marsh of a brackish tidal estuary. Mean bacterial concentrations were slightly higher in flooding (7·1 × 106 cells ml−1) than in ebbing waters (6·5 × 106 cells ml−1), and there were no differences between marshes. Mean chlorophyll a concentrations were 36·7 μg l−1 in the low marsh and 20·4 μg l−1 in the high marsh. Flux calculations, based on tidal records and measured concentrations, suggested a small net import of bacterial and algal biomass into both marshes. Over the course of individual tidal cycles, concentrations of all parameters were variable and not related to tidal stage. Heterotrophic activity measured by the uptake of 3H-thymidine, was found predominantly in the smallest particle size fractions (< 1·0 μm). Thymidine uptake was correlated with temperature (r = 0·48, P < 0·01), and bacterial productivity was estimated to be 7 to 42 μg Cl−1 day−1.  相似文献   

7.
Sediment characteristics, sediment respiration (oxygen uptake and sulphate reduction) and sediment–water nutrient exchange, in conjunction with water column structure and phytoplankton biomass were measured at five stations across the western Irish Sea front in August 2000. The transition from thermally stratified (surface to bottom temperature difference of 2.3 °C) to isothermal water (14.3 °C) occurred over a distance of 13 km. The influence of the front on phytoplankton biomass was limited to a small region of elevated near surface chlorophyll (2.23 mg m−3; 50% > biomass in mixed waters). The front clearly marked the boundary between depositional sediments (silt/clays) with elevated sediment pigment levels (≈60 mg m−2) on the western side, to pigment impoverished (<5 mg m−2) sand, through to coarse sand and shell fragments on the eastern side. Maximal rates of sedimentary respiration on the western stratified side of the front e.g. oxygen uptake S2 (852 μmol O2 m−2 h−1) and sulphate reduction at S1 (149 μmol SO42− m−2 h−1), coupled to significant efflux of nitrate and silicate at the western stations indicate closer benthic–pelagic coupling in the western Irish Sea. Whether this simply reflects the input of phytodetritus from the overlying water column or entrapment and settlement of pelagic production from other regions of the Irish Sea cannot yet be resolved.  相似文献   

8.
The distributions of iodate, iodide and dissolved organic iodine (DOI) were determined in two deep sub-basins in the Chesapeake Bay, the shallow waters at the mouth of the Bay and the adjacent North Atlantic between the late spring and the early fall along the net flow-path of the water entering and exiting the Chesapeake Bay by using an improved analytical scheme designed for the quantitative recovery of DOI. The concentration of R-DOI found in the surface mixed layer in the upper Bay was about twice of those found at the same location in previous studies. (R-X was the concentration of a dissolved iodine species X that had been normalized to a constant salinity of 35.) Thus, DOI in estuarine waters might have been underestimated significantly in the earlier studies. Following the water along its net flow-path, iodate initially constituted more than 60% of total iodine (TI) in the source water in the Middle Atlantic Bight off the Delmarva Peninsula. As this water entered the Chesapeake Bay through the northern part of its mouth, the concentration of R-iodate decreased while that of R-iodide increased progressively until the former became undetectable in the surface mixed layer while the latter reached a maximum of 0.42 μM in the deep water in the upper Bay. Then, the concentration of R-iodate rebounded while that of R-iodide decreased in the outflowing water that exited through the southern part of the mouth of the Bay and was later entrained by the Gulf Stream. The concentration of R-DOI in the surface waters followed the same pattern as R-iodide and reached a maximum of 0.20 μM in the upper Bay. However, R-DOI was depleted in the deep water in the sub-basins. Its concentration dropped to around the detection limit in the suboxic waters in the upper Bay. R-TI in the Bay far exceeded that in the incoming Middle Atlantic Bight water and reached 0.55 μM in the upper Bay. These distributions of the iodine species suggest that, as water from the Middle Atlantic Bight intruded into the Chesapeake Bay, in the well oxygenated surface mixed layer, iodate was reduced to iodide, and the inorganic iodine species could also be converted to DOI. In the deep water, iodate and DOI were converted to iodide. Superimposed on these inter-conversions among the iodine species, dissolved iodine, possibly in the form of iodide, was also added to the water column from the underlying sediments and the process was especially significant in the suboxic deep water in the upper Bay. Mixing between the surface mixed layer and the deep water could also have increased the concentrations of iodide and total iodine in the former.  相似文献   

9.
Concentrations of Hg0 in surface waters and atmosphere of the Scheldt estuary and the North Sea are presented and their relationship with biological processes is discussed. Hg0 concentrations in the Scheldt estuary range from 0.1 to 0.38 pmol·l−1 in the winter and from 0.24 to 0.65 pmol·l−1 in the summer and show a positive relationship with phytoplankton pigments. In the North Sea Hg0 concentrations range from 0.06 to 0.8 pmol·l−1 and are higher in coastal stations. Transfer velocities across the air–sea interface were calculated using a classical shear turbulence model. Volatilization fluxes of Hg0 were calculated for the Scheldt estuary and the North Sea. For the Scheldt estuary the fluxes range from 226–284 pmol·m−2·d−1 in winter and 500–701 pmol·m−2·d−1 in summer and for the North Sea the fluxes range from 59–1110 pmol·m−2·d−1 for an average windspeed of 8.1 m·s−1. These fluxes are comparable to the wet and dry depositional fluxes to the North Sea. Hg0 formation rates necessary to balance the volatilization fluxes vary from 0.2 to 4% d−1.  相似文献   

10.
Dissolved cadmium and copper concentrations have been determined in 76 surface water samples in coastal and ocean waters around Scotland by anodic stripping voltammetry (ASV). A trace metal/salinity ‘front’ is observed to the west, north and north-east of Scotland separating high salinity ocean water (>35 × 10−3) with low concentrations of dissolved Cd and Cu from lower salinity (<35 × 10−3) coastal water containing higher concentrations of Cd and Cu. Mean Cd concentrations in ocean and coastal waters are 7 ng dm−3 (0·06 n ) and 11 ng dm−3 (0·10 n ) respectively; for Cu the respective levels are 60 ng dm−3 (0·95 n ) and 170 ng dm−3 (2·68 n ). The observed distribution is attributed principally to freshwater runoff and the advection of contaminated Irish Sea water into the study area.  相似文献   

11.
The detailed distribution of algal chlorophyll and carotenoid pigments was determined around the halocline (freshwater-seawater interface) in the Krka Estuary on the east coast of the Adriatic Sea; in May 1988. After collection of water along the estuary, particulate matter was extracted and analyzed for pigments by high-performance liquid chromatography coupled with absorbance and fluorescence detection. Bottom marine waters were characterized by lower chlorophyll a (chl a) concentrations than encountered in surface waters, decreasing downstream from 0.50 μg l−1 to 0.16 μg l−1 at the marine end-member. The highest concentrations of chl α (up to 26.34 μg l−1) were found in the interfacial layer, an particularly at one station located off the city of ibenik, where high inputs of nutrients supported the accumulation of living algae at the halocline. Fucoxanthin was the most abundant carotenoid, which indicates a euryhaline dominance of diatoms in the estuary, whereas the dinoflagellate-derived carotenoid peridinin was confined to the interfacial and bottom saline waters of the inner estuary. High concentrations of alloxanthin and chl b were found in the interfacial layer, which also suggests an accumulation of Cryptophyceae and green algae in the inner estuary. Phaeophorbides showed higher concentrations in bottom waters than in surface waters, whereas the highest concentrations occurred in the interfacial layer. These high levels could reflect a density trapping of dead cells in an early degradation state, as suggested by the importance of allomerized chl a and chlorophyllide a vs. total chl a, or of faecal pellets originating from zooplankton grazing in the interfacial layer.  相似文献   

12.
Shipboard incubations from the US JGOFS cruise to the Arabian Sea (TN045) March, 1995 showed evidence of iodate reduction in 0.45 μ (Gelman Supor membrane) filtered seawater samples collected from intermediate depths (200–600 m) within the oxygen minimum zone (OMZ). Inorganic chemical reduction of iodate in these samples was ruled out as no free sulfide was measurable and concentrations of ammonia and nitrite were found to be less than 5 μM. To examine whether the reduction of iodate observed at sea could have been the result of bacterial metabolism, reduction of iodate (IO3) to iodide (I) by Shewanella putrefaciens strain MR-4 was studied in artificial seawater using electrochemical methods. MR-4 is a ubiquitous marine bacterium which may be of considerable importance when considering redox zonation in the water column because it is a facultative anaerobe and may switch amongst a suite of electron acceptors to support metabolism. In all experiments MR-4 reduced all iodate to iodide. The rate of formation of [I]in the culture followed pseudo-first order kinetics. This is the first report of the marine bacterial reduction of iodate where the concentrations of iodide and iodate were measured directly. Our results may help to explain the depth distribution of iodine speciation reported in productive waters like the Arabian Sea and for the first time couple iodine speciation with bacterial productivity in the ocean.  相似文献   

13.
Suspended particle dynamics were investigated in the Ogeechee River Estuary during neap tide in July 1996. Samples were operationally separated into ‘ truly suspended ’ (settling velocity <0·006 cm s−1) and ‘ settleable ’ (settling velocity >0·006 cm s−1) fractions over the course of a tidal cycle to determine whether these two fractions were comprised of particles with differing biological and chemical characteristics. Total suspended sediment, organic carbon and nitrogen, chlorophyll a and phaeopigment concentrations were measured in each fraction, as well as rates of bacterial hydrolytic enzyme activity [β-1,4-glucosidase (βGase) and β-xylosidase (βXase)]. The majority of the suspended sediment (by weight) was in the truly suspended fraction; all measured parameters were largely associated with this fraction as well. When compared to the settleable material, the truly suspended material was significantly higher in % POC (5·7±0·6 vs. 3·9±1·8), % chlorophyll (0·07±0·02 vs. 0·03±0·01), % phaeopigment (0·030±0·006 vs. 0·018±0·012), and weight-specific maximal uptake rates (Vmaxper mg suspended sediment) of both enzymes (1·8±0·4 vs. 0·7± 0·2 nmol mg−1 h−1βGase and 1·1±0·3vs . 0·3±0·2 nmol mg−1 h−1βXase), providing clear evidence for a qualitative distinction between the two fractions. These results are interpreted to mean that the more organic-rich, biologically active material associated with the suspended fraction is likely to have a different fate in this Estuary, as ‘ truly suspended ’ sediments will be readily transported whereas ‘ settleable ’ sediments will settle and be resuspended with each tide. These types of qualitative differences should be incorporated into models of particle dynamics in estuaries.  相似文献   

14.
During nine field transplant tests in San Diego Bay (1987–1990), juvenile mussels were exposed to mean concentrations of tributyltin (TBT) in ambient seawater ranging from 2 to 530 ng liter−1 for 12 weeks under natural conditions. A total of 79 cages with 18 mussels each were monitored at 18 different sites. Growth and seawater TBT concentrations were measured weekly or on alternate weeks (biweekly). Mean growth rates ranged from 17 to 505 mg week−1 (0·2 to 2·5 mm week−1). Accumulation of TBT in mussel tissues was measured at the end of each 12-week test exposure and ranged from 0·1 to 3·2 μg g−1 TBT wet weight. The frequency of the measurements and the integration of chemical and biological measurements improved the accuracy of the assessment over more traditional approaches. Growth was significantly related to seawater and tissue TBT. The statistical relationships with growth effects were used to estimate chemical effect zones for TBT in San Diego Bay. Site-specific differences were distinguished by additional statistical analyses and consideration of environmental significance.  相似文献   

15.
W. Koeve   《Marine Chemistry》2001,74(4):96
Observations of wintertime nutrient concentrations in surface waters are scarce in the temperate and subarctic North Atlantic Ocean. Three new methods of their estimation from spring or early summer observations are described and evaluated. The methods make use of a priori knowledge of the vertical distribution of oxygen saturation and empirical relationships between nutrient concentrations and oxygen saturation. A south–north increase in surface water winter nutrient concentration is observed. Winter nitrate concentrations range from very low levels of about 0.5 μmol dm−3 at 33°N to about 13.5 μmol dm−3 at 60°N. Previous estimates of winter nitrate concentrations have been overestimates by up to 50%. At the Biotrans Site (47°N, 20°W), a typical station in the temperate Northeast Atlantic, a mean winter nitrate concentration of 8 μmol dm−3 is estimated, compared to recently published values between 11 and 12.5 μmol dm−3. It is shown that most of the difference is due to a contribution of remineralised nitrate that had not been recognized in previous winter nutrient estimates. Mesoscale variation of wintertime nitrate concentrations at Biotrans are moderate (less than ±15% of the regional mean value of about 8 μmol dm−3). Interannual variation of the regional mean is small, too. In the available dataset, there was only 1 year with a significantly lower regional mean winter nitrate concentration (7 μmol dm−3), presumably due to restricted deep mixing during an atypically warm winter. The significance of winter nitrate estimates for the assessment of spring-bloom new production and the interpretation of bloom dynamics is evaluated. Applying estimates of wintertime nitrate concentrations of this study, it is found that pre-bloom new production (0.275 mol N m−2) at Biotrans almost equals spring-bloom new production (0.3 mol N m−2). Using previous estimates of wintertime nitrate yields unrealistically high estimates of pre-bloom new production (1.21–1.79 mol N m−2) which are inconsistent with observed levels of primary production and the seasonal development of biomass.  相似文献   

16.
Physical forcing plays a major role in determining biological processes in the ocean across the full spectrum of spatial and temporal scales. Variability of biological production in the Bay of Bengal (BoB) based on basin-scale and mesoscale physical processes is presented using hydrographic data collected during the peak summer monsoon in July–August, 2003. Three different and spatially varying physical processes were identified in the upper 300 m: (I) anticyclonic warm gyre offshore in the southern Bay; (II) a cyclonic eddy in the northern Bay; and (III) an upwelling region adjacent to the southern coast. In the warm gyre (>28.8 °C), the low salinity (33.5) surface waters contained low concentrations of nutrients. These warm surface waters extended below the euphotic zone, which resulted in an oligotrophic environment with low surface chlorophyll a (0.12 mg m−3), low surface primary production (2.55 mg C m−3 day−1) and low zooplankton biovolume (0.14 ml m−3). In the cyclonic eddy, the elevated isopycnals raised the nutricline upto the surface (NO3–N > 8.2 μM, PO4–P > 0.8 μM, SiO4–Si > 3.5 μM). Despite the system being highly eutrophic, response in the biological activity was low. In the upwelling zone, although the nutrient concentrations were lower compared to the cyclonic eddy, the surface phytoplankton biomass and production were high (Chl a – 0.25 mg m−3, PP – 9.23 mg C m−3 day−1), and mesozooplankton biovolume (1.12 ml m−3) was rich. Normally in oligotrophic, open ocean ecosystems, primary production is based on ‘regenerated’ nutrients, but during episodic events like eddies the ‘production’ switches over to ‘new production’. The switching over from ‘regenerated production’ to ‘new production’ in the open ocean (cyclonic eddy) and establishment of a new phytoplankton community will take longer than in the coastal system (upwelling). Despite the functioning of a cyclonic eddy and upwelling being divergent (transporting of nutrients from deeper waters to surface), the utilization of nutrients leading to enhanced biological production and its transfer to upper trophic levels in the upwelling region imply that the energy transfer from primary production to secondary production (mesozooplankton) is more efficient than in the cyclonic eddy of the open ocean. The results suggest that basin-scale and mesoscale processes influence the abundance and spatial heterogeneity of plankton populations across a wide spatial scale in the BoB. The multifaceted effects of these physical processes on primary productivity thus play a prominent role in structuring of zooplankton communities and could consecutively affect the recruitment of pelagic fisheries.  相似文献   

17.
Factors controlling the timing of major (>10 mg chlorophyll a m−3) spring bloom events in the estuarine waters of the Solent, on the south coast of the UK, have been investigated. Winter to summer variations in chlorophyll a concentration together with relevant meteorological and hydrographical data have been analysed for 5 years (1988, 1992, 2001, 2002 and 2003). Mean water column irradiance is demonstrated to be the main factor controlling the timing of the first major spring bloom event, usually dominated by large chain-forming diatoms. When chlorophyll a concentration first exceeds 10 mg m−3 in spring (usually in May) the mean water column photosynthetic active radiation (PAR) averaged for one week prior to the sampling date was always >380 W h m−2 d−1. Prior to the main spring bloom event surface incident radiation and water turbidity combine to limit chlorophyll a concentration to levels <10 mg m−3. Chlorophyll a concentrations >10 mg m−3 do not occur in the Solent until almost the entire 10 m water column is within the euphotic zone (i.e. above 1% light level) and light extinction coefficient (k) is ca. ≤0.5 m−1. Statistically, river flow explains the largest percentage of the variations in k and the delayed bloom in June 2002 is due to increased cloud cover and high levels of rainfall in May, which caused a reduction in surface incident irradiance and increased turbidity. Chlorophyll a peaks during these major bloom events generally occur on spring tides when increased mixing rates favour net growth of diatoms.  相似文献   

18.
Seasonal and diurnal reduced sulfur gas emissions were measured along a salinity gradient in Louisiana Gulf Coast salt, brackish and freshwater marshes. Reduced sulfur gas emission was strongly associated with habitat and salinity gradient. The dominant emission component was dimethyl sulfide (average: 57·3 μg S m−2 h−1) in saltmarsh with considerable seasonal (max: 144·03 μg S m−2 h−1; min: 1·47 μg S m−2 h−1) and diurnal (max: 83·58 μg S m−2 h−1; min: 69·59 μg S m−2 h−1) changes in flux rates. Hydrogen sulfide was dominant (average: 21·2 μg S m−2 h−1, max: 79·2 μg S m−2 h−1; min: 5·29 μg S m−2 h−1) form in brackishmarsh and carbonyl sulfide (average: 1·09 μg S m−2 h−1; max: 3·42 μg S m−2 h−1; min: 0·32 μg S m−2 h−1) was dominant form in freshwater marsh. A greater amount of H2S was evolved from brackishmarsh (21·22 μg S m−2 h−1) as compared to the saltmarsh (2·46 μg S m−2 h−1) and freshwater marsh (0·30 μg S m−2 h−1). Emission of total reduced sulfur gases decreased with decrease in salinity and distance inland from the coast. Emission of total reduced sulfur gases over the study averaged 73·3 μg S m−2 h−1 for the saltmarsh, 32·1 μg S m−2 h−1 for brackishmarsh and 2·76 μg S m−2 h−1 for the freshwater marsh.  相似文献   

19.
Benthic Denitrification in the Gulf of Bothnia   总被引:1,自引:0,他引:1  
Denitrification was measured over an 8-month period in the Bothnian Bay and the Bothnian Sea, the two northernmost basins of the Baltic Sea. The recorded rates varied between 0 and 0·94 mmol N m−2day−1. In the Bothnian Sea, a seasonal pattern could be discerned with high rates in spring, no rate in summer and a moderate rate in winter. In the Bothnian Bay, no such seasonality was observed. It is suggested that denitrification in the Gulf of Bothnia is regulated by sediment nitrification. Calculation of annual mean rates of denitrification gave that the amount of nitrogen consumed by denitrification corresponded to 1·45×104tons N year−1for the Bothnian Bay and 3·45×104tons N year−1for the Bothnian Sea. A comparison with total N input (river runoff, point sources and atmospheric deposition) to the two basins showed that the proportion of N removed through denitrification amounted to 23% for the Bothnian Bay and 31% for the Bothnian Sea.  相似文献   

20.
Dissolved oxygen in seawater has been determined by using the Winkler's reaction scheme for decades. An interference in this reaction scheme that has been heretofore overlooked is the presence of naturally occurring iodate in seawater. Each mole of iodate can result in an apparent presence of 1.5 mol of dissolved oxygen. At the concentrations of iodate in the surface and deep open ocean, it can lead to an overestimation of 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 of oxygen in these waters respectively. In coastal and inshore waters, the effect is less predictable as the concentration of iodate is more variable. The solubility of oxygen in seawater was likely overestimated in data sources that were based on the Winkler's reaction scheme for the determination of oxygen. The solubility equation of García and Gordon [Garcia H.E., Gordon, L.I., 1992. Oxygen solubility in seawater: Better fitting equations. Limnol. Oceanogr. 37, 1307–1312] derived from the results of Benson and Krause [Benson, F.B., Krause, D. Jr., 1984. The concentration and isotopic fractionation of oxygen dissolved in freshwater and seawater in equilibrium with the atmosphere. Limnol. Oceanogr. 29, 620–632] is free from this source of error and is recommended for general use. By neglecting the presence of iodate, the average global super-saturation of oxygen in the surface oceans and the corresponding efflux of oxygen to the atmosphere both have been overestimated by about 8%. Regionally, in areas where the degree of super-saturation or under-saturation of oxygen in the surface water is small, such as in the tropical oceans, the net air–sea exchange flux can be grossly under- or overestimated. Even the estimated direction of the exchange can be reversed. Furthermore, the presence of iodate can lead to an overestimation of the saturation anomaly of oxygen in the upper ocean attributed to biological production by 0.23 ± 0.07%. AOU may have been underestimated by 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 in the surface mixed layer and deep water, while preformed phosphate and preformed nitrate may have been overestimated by 0.004 ± 0.001 and 0.06 ± 0.02 μmol kg− 1 in the surface mixed layer, and 0.005 ± 0.0004 and 0.073 ± 0.006 μmol kg− 1 in the deep water. These are small but not negligible corrections, especially in areas where the values of these parameters are small. At the increasing level of sophistication in the interpretation of oxygen data, this source of error should now be taken into account. Nevertheless, in order to avoid confusion, an internationally accepted standard needs to be adopted before these corrections can be applied.  相似文献   

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