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1.
A mass balance for the naturally-occurring radium isotopes (224Ra, 223Ra, 228Ra, and 226Ra) in Jamaica Bay, NY, was conducted by directly estimating the individual Ra contributions of wastewater discharge, diffusion from fine-grained subtidal sediments, water percolation through marshes, desorption from resuspended particles, and water exchange at the inlet. The mass balance revealed a major unknown source term accounting for 19–71% of the total Ra input, which could only be resolved by invoking a source from submarine groundwater. Shallow (< 2 m depth) groundwater from permeable sediments in Jamaica Bay was brackish and enriched in Ra relative to surface bay waters by over two orders of magnitude. To balance Ra fluxes, a submarine groundwater input of 0.8 × 109–9.0 × 109 L d− 1 was required. This flux was similar for all four isotopes, with individual estimates varying by less than a factor of 2. Our calculated groundwater flux was 6- to 70-fold higher than the fresh groundwater discharge to the bay estimated by hydrological methods, but closely matched direct flow rates measured with seepage meters. This suggests that a substantial portion of the discharge consisted of recirculated seawater. The magnitude of submarine groundwater discharge varied seasonally, in the order: summer > autumn > spring. Chemical analyses suggest that the recirculated seawater component of submarine groundwater delivers as much dissolved nitrogen to the bay as the fresh groundwater flux.  相似文献   

2.
Submarine groundwater discharge (SGD) is now recognized as an important pathway for water and chemical species fluxes to the coastal ocean. In order to determinate SGD to the Gulf of Lion (France), we measured the activities of 226Ra and 228Ra by thermal ionization mass spectrometry (TIMS) in coastal waters and in the deep aquifer waters of the Rhone deltaic plain after pre-concentration of radium by MnO2. Compared to conventional counting techniques, TIMS requires lower quantities of water for the analyses, and leads to higher analytical precision. Radium isotopes were thus measured on 0.25–2 L water samples containing as little as 20 fg of 226Ra and 0.2–0.4 fg of 228Ra with precision equal to 2%. We demonstrate that coastal surface waters samples are enriched in 226Ra and 228Ra compared to the samples further offshore. The high precision radium measurements display a small but significant 226Ra and 228Ra enrichment within a strip of circa 30 km from the coast. Radium activities decrease beyond this region, entrained in the northern current along the shelf break or controlled by eddy diffusion. The radium excess in the first 30 km cannot be accounted for by the river nor by the early diagenesis. The primary source of the radium enrichment must therefore be ascribed to the discharge of submarine groundwater. Using a mass-balance model, we estimated the advective fluxes of 226Ra and 228Ra through SGD to be 5.2 × 1010 and 21 × 1010 dpm/d respectively. The 226Ra activities measured in the groundwater from the Rhone deltaic plain aquifer are comparable to those from other coastal groundwater studies throughout the world. By contrast, 228Ra activities are higher by up to one order of magnitude. Taking those groundwater radium activities as typical of the submarine groundwater end-member, a minimum volume of 0.24–4.5 × 1010 l/d is required to support the excess radium isotopes on the inner shelf. This has to be compared with the average rivers water runoff of 15.4 × 1010 l/d during the study period (1.6 to 29% of the river flow).  相似文献   

3.
The Patos–Mirim Lagoon system along the southern coast of Brazil is linked to the coastal ocean by a narrow mouth and by groundwater transport through a Holocene barrier. Although other groundwater systems are apparently active in this region, the hydraulic head of the lagoon, the largest in South America, drives groundwater transport to the coast. Water levels in wells placed in the barrier respond to changing water level in the lagoon. The wells also provide a measure of the nutrient concentrations of groundwater flowing toward the ocean. Additionally, temporary well points were used to obtain nutrient samples in groundwater on the beach face of the barrier. These samples revealed a subterranean freshwater–seawater mixing zone over a ca. 240 km shoreline. Previously published results of radium isotopic analyses of groundwater and of surface water from cross-shelf transects were used to estimate a water flux of submarine groundwater discharge (SGD) to nearshore surface waters of 8.5 × 107 m3/day. Using this SGD and the nutrient concentrations in different compartments, nutrient fluxes between groundwater and surface water were estimated. Fluxes were computed using both average and median reservoir (i.e. groundwater and surface water) nutrient concentrations. The SGD total dissolved inorganic nitrogen, phosphate and silicate fluxes (2.42, 0.52, 5.92 × 106 mol day− 1, respectively) may represent as much as 55% (total N) to 10% (Si) of the nutrient fluxes to the adjacent shelf environment. Assuming nitrogen limitation, SGD may be capable of supporting a production rate of ca. 3000 g C m2 year− 1in the nearshore surf zone in this region.  相似文献   

4.
We discuss nitrous oxide (N2O) and methane (CH4) distributions in 49 vertical profiles covering the upper ∼300 m of the water column along two ∼13,500 km transects between ∼50°N and ∼52°S during the Atlantic Meridional Transect (AMT) programme (AMT cruises 12 and 13). Vertical N2O profiles were amenable to analysis on the basis of common features coincident with Longhurst provinces. In contrast, CH4 showed no such pattern. The most striking feature of the latitudinal depth distributions was a well-defined “plume” of exceptionally high N2O concentrations coincident with very low levels of CH4, located between ∼23.5°N and ∼23.5°S; this feature reflects the upwelling of deep waters containing N2O derived from nitrification, as identified by an analysis of N2O, apparent oxygen utilization (AOU) and NO3, and presumably depleted in CH4 by bacterial oxidation. Sea-to-air emissions fluxes for a region equivalent to ∼42% of the Atlantic Ocean surface area were in the range 0.40–0.68 Tg N2O yr−1 and 0.81–1.43 Tg CH4 yr−1. Based on contemporary estimates of the global ocean source strengths of atmospheric N2O and CH4, the Atlantic Ocean could account for ∼6–15% and 4–13%, respectively, of these source totals. Given that the Atlantic Ocean accounts for around 20% of the global ocean surface, on unit area basis it appears that the Atlantic may be a slightly weaker source of atmospheric N2O than other ocean regions but it could make a somewhat larger contribution to marine-derived atmospheric CH4 than previously thought.  相似文献   

5.
分别于2006年8月,12月和2007年4月,10月采集胶州湾及周边海域大气和海水样品,对氧化亚氮(N2O)和甲烷(CH4)浓度进行了测定,并设置1个连续站进行24 h连续观测.结果表明:大气中N2O春、夏、秋、冬的平均浓度(体积分数)分别为(3.17±0.03)×10-7,(3.24±0.15)×10-7,(3.19±0.02)×10-7和(3.08±0.25)×10-7;大气中CH4春、夏、秋、冬的平均浓度(体积分数)分别为(1.89±0.04)×10-6,(1.79±0.04)×10-6,(2.09±0.21)×10-6和(2.01±0.09)×10-6.胶州湾表、底层海水中N2O和CH4的浓度和饱和度表现出明显的季节变化,其中N2O浓度和饱和度冬季最高,春、秋季次之,夏季最低;CH4浓度和饱和度夏季最高,冬季最低.利用Liss and Merlivat(1986)公式和Wanninkhof(1992)公式估算出胶州湾海域N2O的年平均海-气交换通量分别为(11.16±14.15)和(22.42±27.56)μmol m-2·d-1;CH4分别为(7.75±6.19)和(17.76±14.84)μmol m-2·d-1.胶州湾大部分海域表层海水中N2O和CH4呈过饱和状态,是大气中N2O和CH4的净源.  相似文献   

6.
Nutrient fluxes were measured between Fourleague Bay, a shallow Louisiana estuary, and the Gulf of Mexico every 3 h between February 1 and April 30, 1994 to determine how high velocity winds associated with cold fronts and peak Atchafalaya River discharge influenced transport. Net water fluxes were ebb-dominated throughout the study because of wind forcing and high volumes of water entering the northern Bay from the Atchafalaya River. Flushing time of the Bay averaged <8 days; however, more rapid flushing occurred in response to northerly winds with approximately 56% of the volume of the Bay exported to the Gulf in 1 day during the strongest flushing event. Higher nitrate+nitrite (NO2+NO3), total nitrogen (TN), and total phosphorus (TP) concentrations were indicative of Atchafalaya River input and fluxes were greater when influenced by high velocity northerly winds associated with frontal passage. Net exports of NO2+NO3, TN, and TP were 43.5, 98.5, and 13.6 g s−1, respectively, for the 89-day study. An average of 10.6 g s−1 of ammonium (NH4) was exported to the Gulf over the study; however, concentrations were lower when associated with riverine influence and wind-driven exports suggesting the importance of biological processes. Phosphate (PO4) fluxes were nearly balanced over the study with fairly stable concentrations indicating a well-buffered system. The results indicate that the high energy subsidy provided by natural pulsing events such as atmospheric cold fronts and seasonal river discharge are efficient mechanisms of nutrient delivery to adjacent wetlands and nearshore coastal ecosystems and are important in maintaining coastal sustainability.  相似文献   

7.
This paper reports the initial results of a study of groundwater and coastal waters of southern Brazil adjacent to a 240 km barrier spit separating the Patos Lagoon, the largest coastal lagoon in South America, from the South Atlantic Ocean. The objective of this research is to assess the chemical alteration of freshwater and freshwater–seawater mixtures advecting through coastal permeable sands, and the influence of the submarine discharge of these fluids (SGD) on the chemistry of coastal waters. Here we focus on dissolved iron in this system and use radium isotopic tracers to quantify SGD and cross-shelf fluxes. Iron concentrations in groundwaters vary between 0.6 and 180 μM. The influence of the submarine discharge of these fluids into the surf zone produces dissolved Fe concentrations as high as several micromolar in coastal surface waters. The offshore gradient of dissolved Fe, coupled with results for Ra isotopes, is used to quantify the SGD flux of dissolved Fe from this coastline. We estimate the SGD flux to be 2 × 106 mol day− 1 and the cross-shelf flux to be 3.2 × 105 mol day− 1. This latter flux is equal to about 10% of the soluble atmospheric Fe flux to the entire South Atlantic Ocean. We speculate on the importance of this previously unrecognized iron input to regional ocean production and on the potential significance of this source to understanding variations in glacial–interglacial ocean production.  相似文献   

8.
《Oceanologica Acta》2003,26(4):421-433
Shelf-slope exchanges and budgets of organic and inorganic nutrients are calculated for the Gulf of Lion continental margin in the northwestern Mediterranean. Computations are based on data from three seasonal marine surveys performed in March 1998, June 1998 and January 1999 in the framework of the French Programme National d’Environnement Côtier. A Land-Ocean Interactions in the Coastal Zone type box model is used to calculate the advective exchanges between the shelf and the adjacent open sea and to estimate the budgets of non-conservative elements (DIP, DIN, DOP, DON, DOC, POC, PON, POP). These budgets consider river discharges, urban sewage supply, atmospheric deposition, and fluxes at the water-sediment and shelf-slope interfaces. Uncertainties on the fluxes and budgets are estimated to assess the robustness of the results with respect to the spatial variability of the system. Results indicate that shelf-slope exchanges by mixing predominate with respect to the major input terms (river discharge and sediment release). Budgets for inorganic nutrients, that show a strong concentration gradient between the shelf and the slope waters, are significantly different from zero and indicate an excess of these elements in the shelf water. For all surveys, these surpluses suggest (i) that the whole shelf system is autotrophic (1.6–4.3 × 103 mol C s–1) and acts as a sink of CO2, and (ii) that it is a site of net denitrification (119 mol N s–1) and acts as a sink of N2. Average shelf-slope fluxes of dissolved and particulate organic elements generally indicate an export to the open sea. However, the large uncertainty on these fluxes yields budgets for the shelf not significantly different from zero.  相似文献   

9.
We conducted studies of nutrients and water mass movements in a semi-enclosed bay in northern China to understand nutrient dynamics under varying tidal regimes. Four cruises were conducted under varying tidal regimes in Jiaozhou Bay, two at neap tide and one at spring tide in August and one at spring tide in October 2001. In addition to transect surveys, drift experiments and an anchor station were employed to show current and tidal effects. Samples for nutrient evaluation were taken from the five major tributary rivers in March (dry season) and August (flood season) of 2002 to estimate nutrient transport by rivers, and wastewater samples were collected to evaluate nutrients in wastewater discharge. Benthic nutrient fluxes were determined by (1) incubation of sediments with overlying seawater on board the boat and (2) calculated by Fick’s First Law from nutrient pore water profiles. Nutrient concentrations were high in the north, especially the northeast and northwest sectors, reflecting human activities. Jiaozhou Bay was characterized by high nitrogen, but low phosphorus and silica concentrations compared to Chinese coastal seas. Based on nutrient atomic ratios, the limiting elements for phytoplankton growth in Jiaozhou Bay were silica and phosphorus. The fluxes of nutrients between sediment and overlying water varied depending on the specific nutrient, the site and redox conditions. Benthic nutrient fluxes based on sediment incubations were all lower than the estimated diffusive fluxes, implying that the nutrients released from sediment pore waters were probably utilized by benthic microalgal and bottom-water primary production. A preliminary estimate of nutrient budgets demonstrated that riverine and wastewater inputs were greater than atmospheric deposition into Jiaozhou Bay, except that nitrate from wastewater inputs was less than atmospheric deposition. Concentrations of nitrogen and phosphorus increased while silica decreased in the last four decades, similar to other eutrophicated estuaries. The resulting shift in nutrient composition in Jiaozhou Bay affects phytoplankton composition, trophic interactions, and sustainability of living resources.  相似文献   

10.
Pore Water Nutrient Regeneration in Shallow Coastal Bohai Sea, China   总被引:1,自引:0,他引:1  
The regeneration of pore water nutrients was studied and the contribution of benthic nutrient fluxes to the overlying water was evaluated on the basis of field specific observations conducted in September–October 1998 and April–May 1999 in the Bohai Sea. Nutrient concentrations in sediment pore waters were examined by incubating sediment core samples with overlying seawater in air and/or nitrogen conditions. Nutrient diffusion fluxes calculated by diagenetic equations were within a factor of 2 during incubations. The factors affecting nutrient diffusion across sediment/water interface include bioturbation, nitrification, denitrification, adsorption, and dissolution. The regeneration of nutrients from sediments will increase nutrient loads of the Bohai Sea and affect nutrient atomic ratios in this region. Among nutrient sources from riverine input, atmospheric deposition and sediment regeneration, ammonium and phosphate mainly came from atmospheric deposition (>50%); nitrate was mainly transported by riverine input into the Sea, silicate from sediment regeneration accounts up to 60%. This demonstrates that nutrient regeneration in sediments contributes more silicate than riverine input and atmospheric deposition together, but benthic flux contributes very much less phosphate and nitrate relative to riverine input and atmospheric deposition. The benthic fluxes of nutrients may lead to a decrease of the amount of nitrate, an increase of phosphate, ammonia and silicate in the water column. The release of silicate from sediments may compensate the decrease of silicate due to the reduction of riverine discharge. Nutrient regeneration in sediment may have an important influence on the eutrophic character of coastal waters in this region. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

11.
The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N2O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N2O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO3) and nitrite (NO2) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N2O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N2O, NO3 and NO2 were lower than in the overlying water. In most East China Sea sediments, both N2O and NO3 decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N2O and NO3 consumption by denitrification at anoxic microsites. N2O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N2O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N2O and NO3 in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m−2 h−1 in Koaziro Bay in the spring, −29 to −21 nmolN m−2 h−1 in the summer, −46 to 37 nmolN m−2 h−1 in the East China Sea, 0.17 to 0.23 nmolN m−2 h−1 in the equatorial Pacific, and <±0.2 nmolN m−2 h−1 in the subtropical North Pacific, respectively.  相似文献   

12.
N2O Production, Nitrification and Denitrification in an Estuarine Sediment   总被引:1,自引:0,他引:1  
The mechanisms regulating N2O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N2O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with15N tracer (15N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m−2 h−1and 214 to 1260 μmol N m−2 h−1, respectively), while benthic N2O evolution decreased slightly (1560 to 1250 nmol N m−2 h−1). Apparent diffusion coefficients of inorganic nitrogen compounds and O2at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O2supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N2O production through nitrification, the observed decrease in sedimentary N2O production seems to be attributed to the decrease in N2O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N2O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N2O production in nearshore sediments.  相似文献   

13.
Benthic fluxes of dissolved inorganic carbon, total alkalinity, oxygen, nutrients, nitrous oxide and methane were measured in situ at three sites of Río San Pedro salt marsh tidal creek (Bay of Cádiz, SW Spain) during three seasons. This system is affected by the discharges of organic carbon and nutrients from the surrounding aquaculture installations. Sediment oxygen uptake rates and inorganic carbon fluxes ranged respectively from 16 to 79 mmol O2 m? 2 d? 1 and from 48 to 146 mmol C m? 2 d? 1. Benthic alkalinity fluxes were corrected for the influence of NH4+ and NO3? + NO2? fluxes, and the upper and lower limits for carbon oxidation rates were inferred by considering two possible scenarios: maximum and minimum contribution of CaCO3 dissolution to corrected alkalinity fluxes. Average Cox rates were in all cases within ± 25% of the upper and lower limits and ranged from 40 to 122 mmol C m? 2 d? 1. Whereas carbon mineralization did not show significant differences among the sites, Cox rates varied seasonally and were correlated with temperature (r2 = 0.72). During winter and spring denitrification was estimated to account for an average loss of 46% and 75%, respectively, of the potentially recyclable N, whereas during the summer no net removal was observed. A possible shift from denitrification to dissimilatory nitrate reduction to ammonium (DNRA) during this period is argued. Dissolved CH4 and N2O fluxes ranged from 5.7 to 47 μmol CH4 m? 2 d? 1 and 4.3 to 49 μmol N–N2O m? 2 d? 1, respectively, and represented in all cases a small fraction of total inorganic C and N flux. Overall, about 60% of the total particulate organic matter that is discharged into the creek by the main fish farm facility is estimated to degrade in the sediments, resulting in a significant input of nutrients to the system.  相似文献   

14.
胶州湾潮汐潮流动边界数值模拟   总被引:11,自引:4,他引:7  
基于普林斯顿海洋模式,通过干湿网格判别法引入潮汐潮流的漫滩过程,考虑M2,S2,K1,O1,M4和MS4六个主要分潮,建立了胶州湾潮汐潮流数值模拟和预报模型,研究了该海域潮汐潮流特征,并讨论了漫滩对潮流模拟的影响。与实测资料的对比验证表明,该模式能够对胶州湾的潮汐和潮流做出较为合理的预测。给出了胶州湾潮汐、潮流、余流等分布特征,模拟的潮流场以及余流场涡旋等现象与观测符合良好;计算了潮波能通量,从能量角度探讨了潮波的传播特性;对潮位与潮流场演变规律,以及潮能通量的分析表明,胶州湾内的潮波以驻波为主。通过数值试验发现,漫滩过程的引入对胶州湾潮流速度的模拟至关重要,不考虑漫滩过程的模式会夸大或者低估潮流流速。对于滩涂面积广阔的海域来说,潮流数值模式中考虑漫滩的影响是必要的。  相似文献   

15.
Atmospheric dry deposition of nitrogen (N) and dinitrogen (N2) fixation rates were assessed in 2004 at the time-series DYFAMED station (northwestern Mediterranean, 43°25′N, 7°52′E). The atmospheric input was monitored over the whole year. Dinitrogen fixation was measured during different seasonal trophic states (from mesotrophy to oligotrophy) sampled during nine cruises. The bioavailability of atmospherically deposited nutrients was estimated by apparent solubility after 96 h. The solubility of dry atmospheric N deposition was highly variable (from ∼18% to more than 96% of total N). New N supplied to surface waters by the dry atmospheric deposition was mainly nitrate (NO3) (∼57% of total N, compared to ∼6% released as ammonium (NH4+)). The mean bioavailable dry flux of total N was estimated to be ∼112 μmol m−2 d−1 over the whole year. The NO3 contribution (70 μmol NO3 m−2 d−1) was much higher than the NH4+ contribution (1.2 μmol NH4+ m−2 d−1). The N:P ratios in the bioavailable fraction of atmospheric inputs (122.5–1340) were always much higher than the Redfield N:P ratio (16). Insoluble N in atmospheric dry deposition (referred to as “organic” and believed to be strongly related to anthropogenic emissions) was ∼40 μmol m−2 d−1. N2 fixation rates ranged from 2 to 7.5 nmol L−1 d−1. The highest values were found in August, during the oligotrophic period (7.5 nmol L−1 at 10 m depth), and in April, during the productive period (4 nmol L−1 d−1 at 10 m depth). Daily integrated values of N2 fixation ranged from 22 to 100 μmol N m−2 d−1, with a maximum of 245 μmol N m−2 d−1 in August. No relationship was found between the availability of phosphorus or iron and the observed temporal variability of N2 fixation rates. The atmospheric dry deposition and N2 fixation represented 0.5–6% and 1–20% of the total biological nitrogen demand, respectively. Their contribution to new production was more significant: 1–28% and 2–55% for atmospheric dry deposition and N2 fixation, respectively. The dry atmospheric input was particularly significant in conditions of water column stratification (16–28% of new production), while N2 fixation reached its highest values in June (46% of new production) and in August (55%).  相似文献   

16.
桑沟湾养殖海域营养盐和沉积物-水界面扩散通量研究   总被引:7,自引:0,他引:7  
利用2006年4,7,11月和2007年1月4个航次对桑沟湾养殖海域的观测资料,分析了该海域营养盐分布、结构特征、主要控制过程以及沉积物-水界面扩散通量,结果表明,该海域的营养盐分布具有明显的季节变化,海水中NO3-,NO2-,PO43-,DOP,TDP和SiO32-浓度皆是秋季最高,而NH4+,DON,TDN浓度则为夏季最高;各种营养盐的最低值除DON外都出现在春季。春季湾内外海水交换不畅,再加上大型藻类海带等生长旺盛期的消耗,使营养盐浓度处于较低水平,在夏秋两季丰水期沿岸河流注入对该海域营养盐的影响较大,冬季无机营养盐浓度分布主要受沿岸流的影响。磷的结构变化较大,其中DOP百分含量在夏季最高,达到81%。从春季到秋季海水中TDN的结构变化从以DON为主转变成以DIN为主。硅和氮的原子比值全年变化不大,硅和氮和氮和磷原子比值春夏两季的高于秋冬季的。分析营养盐化学计量限制标准和浮游植物生长的最低阈值结果表明,磷是春夏两季桑沟湾浮游植物生长的限制性因素;春季硅浓度低于浮游植物生长的最低阀值,也是一个潜在的限制因素。计算结果显示桑沟湾沉积物释放的NH4+,SiO32-和PO43-对初级生产力的贡献较小,与其他浅海环境相比,桑沟湾沉积物-水界面的营养盐通量处于较低或中等水平。  相似文献   

17.
Mass fluxes of diatom opal, planktonic foraminifera carbonate and coccolithophorid carbonate were measured with time-series sediment traps at six sites in the Arabian Sea, Bay of Bengal and Equatorial Indian Ocean (EIOT). The above fluxes were related to regional variations in salinity, temperature and nutrient distribution. Annual fluxes of diatom opal range between 3 and 28 g m−2 yr−1, while planktonic foraminifera carbonate fluxes range between 6 and 23 g m−2 yr−1 and coccolithophorid carbonate fluxes range between 4 and 24 g m−2 yr−1. Annual planktonic foraminifera carbonate to coccolithophorid carbonate ratios range between 0.8 and 2.2 and coccolithophorid carbonate to diatom opal ratios range between 0.5 and 3.3.In the western Arabian Sea, coccolithophorids are the major contributors to biogenic flux during periods of low nutrient concentrations. Coccolithophorid carbonate fluxes decrease and planktonic foraminiferal carbonate and diatom opal fluxes increase when nutrient-rich upwelled waters are advected over the trap site. In the oligotropic eastern Arabian Sea, coccolithophorid carbonate fluxes are high throughout the year. Planktonic foraminiferal carbonate fluxes are the major contributors to biogenic flux in the EIOT. In the northern and central Bay of Bengal, when surface salinity values drop sharply during the SW monsoon, there is a drastic reduction in planktonic foraminiferal carbonate fluxes, but coccolithophorid carbonate and diatom opal fluxes remain steady or continue to increase. Distinctly higher annual molar Sibio/Cinorg (>1) and Corg/Cinorg (>1.5) ratios are observed in the northern and central Bay of Bengal mainly due to lower foraminiferal carbonate production as a result of sharp salinity variations. We can thus infer that the enhanced freshwater supply from rivers should increase oceanic CO2 uptake. Its silicate supply favours the production of diatoms while the salinity drop produces conditions unfavourable for most planktonic foraminifera species.  相似文献   

18.
Nitrous oxide (N2O) is a trace gas that is increasing in the atmosphere. It contributes to the greenhouse effect and influences the global ozone distribution. Recent reports suggest that regions such as the Arabian Sea may be significant sources of atmospheric N2O.In the ocean, N2O is formed as a by-product of nitrification and as an intermediary of denitrification. In the latter process, N2O can be further reduced to N2. These processes, which operate on different source pools and have different magnitudes of isotopic fractionation, make separate contributions to the 15N and18O isotopic composition of N2O. In the case of nitrification in oxic waters, the isotopic composition of N2O appears to depend mainly on the 15N/14N ratio of NH+4 and the 18O/16O ratio of O2 and H2O. In suboxic waters, denitrification causes progressive 15N and 18O enrichment of N2O as a function of degree of depletion of nitrate and dissolved oxygen. Thus the isotopic signature of N2O should be a useful tool for studying the sources and sinks for N2O in the ocean and its impact on the atmosphere.We have made observations of N2O concentrations and of the dual stable isotopic composition of N2O in the eastern tropical North Pacific (ETNP) and the Arabian Sea. The stable isotopic composition of N2O was determined by a new method that required only 80–100 nmol of N2O per sample analysis. Our observations include determinations across the oxic/suboxic boundaries that occur in the water columns of the ETNP and Arabian Sea. In these suboxic waters, the values of δ15N and δ18O increased linearly with one another and with decreasing N2O concentrations, presumably reflecting the effects of denitrification. Our results suggest that the ocean could be an important source of isotopically enriched N2O to the atmosphere.  相似文献   

19.
为评价胶州湾水体表观年龄和地下水入海通量,2011年9—10月在胶州湾地区分别采集地下水、河水和海水样品,对水样的224Ra和226Ra活度进行测量。基于224Ra和226Ra半衰期的差异,运用224Ra与226Ra的活度比值计算了胶州湾水体表观年龄;采用三端元混合模型计算了胶州湾海水中地下水、河水与湾外海水的混合比例;在水体表观年龄和混合比例的基础上,计算了地下水入海通量。结果表明:研究期间胶州湾水体表观年龄分布范围为3.2—39.4d,平均值为14.7d,呈现从湾顶到湾口年龄逐渐增大的趋势,地下水的平均混合比例是11.0%,地下水的入海通量为7.29×106m3/d,海底地下水排泄速率为3.8cm/d。  相似文献   

20.
Fixed nitrogen is a key nutrient involved in regulating global marine productivity and hence the global oceanic carbon cycle. Oceanic nitrogen (N2) fixation is estimated to supply 8×1012 moles N y?1 to the ocean, approximately equal to current riverine and the atmospheric inputs of fixed N, and between 50 and 100% of current estimates of oceanic denitrification. However, the spatial and temporal variability of N2 fixation remains uncertain, mostly because of the normal low resolution sampling for diazotroph distribution and fixation rates. It is well established that N2 fixation, mediated by the enzyme nitrogenase, is a source of hydrogen (H2), but the extent to which it leads to supersaturation of H2 in oceanic waters is unresolved. Here, we present simultaneous measurements of upper ocean dissolved H2 concentration (nmol L?1), and rates of N2 fixation (μmol N m?3 d?1), determined using 15N2 tracer techniques (at 7 or 15 m), on a transect from Fiji to Hawaii. We find a significant correlation (r=0.98) between dissolved H2 and rates of N2 fixation, with the greatest supersaturation of H2 and highest rates of N2 fixation being observed in the subtropical gyres at the southern (~18°S) and northern (18°N) reaches of the transect. The lowest H2 saturation and N2 fixation were observed in the equatorial region between 8°S and 14°N. We propose that an empirical relationship between H2 supersaturations and N2 fixation measurements could be used to guide sampling for 15N fixation measurements or to aid the spatial interpolation of such measurements.  相似文献   

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