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1.
The concentrations of dissolved organic carbon and nitrogen (DOC and DON, respectively) were measured in Shiraho fringing reef (Japan), using a high-temperature catalytic-oxidation method. When the seawater on the reef flat (shallow lagoon) was isolated from the surrounding ocean due to the low tide, the concentrations of DOC and DON on the reef flat were 66–75 and 4.8–5.7 μmol l−1, respectively. The DOC and DON concentrations were higher than those of the adjacent outer ocean (57–58 and 3.8 μmol l−1, respectively), suggesting that the coral reef functioned as a net source of dissolved organic matter for the surrounding ocean. In order to investigate long-term bacterial decomposition of the reef-derived DOC (RF-DOC), the seawater samples collected on the reef flat and at the adjacent ocean were incubated in the dark for 1 year. Regression analysis using an exponential curve that considered two degradability pools (labile and refractory) fitted the mineralization of the RF-DOC very well (r 2 > 0.89). According to the regression analysis, the DOC produced on the reef flat was composed of the labile fraction of 63–94% (average 77%) and the refractory fraction of 6–37% (average 23%). It was concluded that some of the DOC that was produced in the coral reef ecosystem was exported to the surrounding ocean if the reef flat had a water residence time less than several months. The exported organic matter may support microbial communities in the ocean as an energy source.  相似文献   

2.
Factors controlling the CO2 system parameters, including the partial pressure of CO2 (PCO2) in coral reef waters, were investigated in three mid-oceanic reefs of the Indo-Pacific region. Surface water PCO2 in the lagoons of Majuro Atoll and Palau barrier reef in the Pacific were 25 µatm and 48 µatm higher than those of the offshore waters, respectively, while South Male Atoll lagoon of the Maldives in the Indian Ocean exhibited relatively small difference in PCO2 compared to the offshore water. Observations from Majuro Atoll and Palau barrier reef are consistent with the view that calcium carbonate production predominates in coral reefs. On the other hand, results from South Male Atoll can be attributed to the thorough flushing of the lagoon, which is connected to the open ocean by numerous deep channels. The offshore-lagoon PCO2 difference depends on system-level net organic-to-inorganic carbon production ratio while reef topography, especially residence time of the lagoon, has a secondary effect on the magnitude of the offshore-lagoon difference. A potential for releasing CO2 might be more evident in an enclosed atoll where the reef water has a longer residence time. Oceanic atoll and barrier reef lagoons, which are in the terminal stage of evolutionary history of oceanic volcanic islands, have the potential to release CO2 to the atmosphere.  相似文献   

3.
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   

4.
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   

5.
It is generally assumed that estuarine mixing is continuous for metals from terrestrial sources, gradually decreasing towards the open ocean endmember. Here we show that, chemical reactivity, determined by ion exchange method, and molecular weight distributions, obtained using cross-flow ultrafiltration, of dissolved Cd, Cu, and Ni in the surface waters of the Gulf of Mexico varied systematically across the estuarine mixing zone of the Mississippi River. Most size or chemical affinity fractions of dissolved metals (<0.4 μm) were linearly related to salinity (10.8–36.6), suggesting that the distribution of these elements was mainly controlled by continuous mixing processes. Dissolved concentrations across the salinity gradient ranged for Cd: 87–187 pM; Cu: 1.4–18.3 nM; and Ni: 2.6–18.8 nM, with highest values near the Mississippi river mouth, and lowest concentrations in a warm core ring in the Gulf of Mexico. Dissolved Cd was mostly present as a truly dissolved (<10 kDa, 97 ± 1%) and cationic fraction (Chelex-100 extractable, 94 ± 4%). A novel observation across the estuarine mixing zone was that colloidal metal concentrations were identical to either inert (for Cu, Ni) or AMPG-labile anionic (Cu, Cd) fractions. The difference in behavior between Cu and the other two metals might indicate differences in the biopolymeric nature of the metal–organic chelates. In particular, the anionic-organic Cd fractions accounted for just 3 ± 1%, on average. However, for Cu, it was 24 ± 4%, and for Ni, it was 9 ± 6%. The fractions of the total dissolved metal fractions that were “inert” averaged 31 ± 10% for Cu and 29 ± 12% for Ni. Small but noticeable amounts (6 ± 3%) of dissolved inert Cd fractions were also present. Apparent non-local transport processes, likely associated with cross-shelf sediment resuspension processes, could have been responsible for the relatively high concentrations of ‘inert’ and ‘anionic’ metal fractions in high salinity coastal waters, and accounting for the persistence of metals bound to humic substances in the Gulf of Mexico.  相似文献   

6.
《Marine Chemistry》2002,79(1):1-26
This study investigates the relative importance of processes that affect trace metal (TM) cycling in the upper water column at the shelf edge of the Celtic Sea on the western European continental margin. The examined processes include external inputs (by atmosphere and river), physical factors (upwelling, winter mixing and water mass advection) and biological processes (in situ uptake, regeneration and export to deep waters). The concentrations of dissolved Cd, Cu, Ni and Pb were measured with this aim in January 1994 and June 1995 at vertical stations across slope, including stations with upwelling, and in the surface waters along the Celtic Sea shelf. Additionally, deep sea (from sediment trap data) and atmospheric fluxes were estimated. The metal profiles over the slope off the Celtic Sea are quite similar to open ocean profiles already described in the northeast Atlantic, and the concentrations in surface waters are only slightly enriched compared to the nearby open ocean (1.2–1.3× for Cd and Ni). The external sources to the system appear to be of weak influence: the fluvial input is locally strong at the coast and then “diluted” along the large continental shelf; the atmospheric deposition is not significant at the annual scale in comparison to the metal content in the upper waters of the shelf edge (at least for Cd, Ni and Cu). In the upwelling zone, a significant increase in concentrations was observed in the summer surface mixed layer (×2 for nitrate and Cd and ×1.5 for Ni) in comparison to the non-upwelling zone. In winter, concentrations of bioreactive metals increased significantly in the surface waters in comparison to the low summer levels (×5 for nitrate and Cd). Our results suggest that upwelling and winter mixing act as regenerated sources that lead to the resupply of the bioreactive elements above the permanent thermocline with a low export to deeper waters. The tracing of the Mediterranean intermediate waters (MIW) from Gibraltar to the studied area shows indeed that its elemental content at the Celtic shelf edge is mainly due to the conservative mixing of the three “end-member” component waters which are thought to make up the MIW. The remineralization of organic matter within this water mass during its transport to the north would contribute only 20% of the nutrients and Cd concentrations recorded at the Celtic Sea shelf edge. According to the correlation found with nutrients in the 10–200-m layer, dissolved Pb would also be subjected to biological uptake and regeneration within the seasonal thermocline. Particulate scavenging removal of Pb would take place below the permanent thermocline throughout the water column.  相似文献   

7.
During the August 1993 Intergovernmental Oceanographic Commission's Contaminant Baseline Survey cruise to the high latitude North Atlantic, determinations of total dissolved sulfide (TDS=free sulfide, H2S(g)+HS−+S2−, plus dissolved metal–sulfide complexes), free sulfide, and carbonyl sulfide (OCS) were made along a horizontal transect and at six vertical profile stations. Unlike data from lower latitudes, the distributions of OCS and TDS were remarkably uniform, with surface water OCS averaging 108 pmol/l and TDS averaging 58 pmol/l; free sulfide was below the detection limits of 5 pmol/l at all stations. The vertical profiles of both OCS and TDS show surface maxima and rapid decreases into the major thermocline. For OCS this is indicative of production via photolysis of dissolved organic sulfur compounds, while TDS may be produced from the hydrolysis of OCS. The concentrations of OCS are similar to those found in coastal waters, and suggests that these sub-polar regions may be large OCS sources to the troposphere during summer. However, it is unclear whether higher concentrations of OCS precursors, a long photo period during summer, or slow rates of removal by hydrolysis due to low temperatures are responsible for the elevated OCS levels. TDS concentrations are primarily controlled by the rate of OCS hydrolysis, production by phytoplankton, and oxidative loss by oxygen and iodate. Both of the losses are affected by trace metal complexation, and to examine this, freshly collected seawater was amended by hydrogen sulfide gas and trace metal additions, and the concentration of free sulfide monitored as a function of metal concentration. This allowed the determinations of conditional stability constants for metal sulfides, with the log Kcond of Cd(HS)+ being 8.0±0.5, 7.0±0.6 for Ni(HS)+, and 7.4±0.7 for Zn(HS)+; attempts at measuring the Kcond of Cu(HS)+ were thwarted by the apparent reduction of Cu(II) to Cu(I) by sulfide. Using these constants in an equilibrium speciation model indicates that on average about 75% of the measured TDS was free, with the remaining fraction complexed with Ni, Cd, and Zn (in order of decreasing percentages). While closer to the field observations than would be found with stability constants reported by other workers, these values are still at variance with the actual speciation (i.e., <30% free). This suggests that the stability constants for Cd, Ni, and Zn are somewhat higher than found, thus reducing the concentration of free sulfide. Nevertheless, these speciation data are important for balancing the TDS budget since the loss by iodate oxidation of free sulfide exceeds all production estimates.  相似文献   

8.
南沙渚碧礁生态系有机碳的分布及周日变化特征   总被引：4，自引：0，他引：4  
1999 年 4 月对我国南沙群岛渚碧礁海水中溶解有机碳的分布及礁坪区颗粒有机碳 (POC) 和溶解有机碳 (DOC) 的周日变化特征进行了观测。结果表明,渚碧礁表层海水 DOC 变化范围为 1.43~3.62 mg/L,平均为 2.16 mg/L,含量分布大致表现为礁坪区>潟湖>礁外。潟湖 DOC 的垂直分布大致表现为表层高于底层,可能与表层浮游植物的光合作用有关。礁坪区 POC 及 DOC 都呈现显著的周日变化特征,POC 呈现夜晚高,白天低的特点,浮游植物的昼夜垂直移动可能是产生该现象的主要原因。DOC 的周日变化则主要受浮游动物昼夜垂直移动及细菌等生物活动的影响。  相似文献   

9.
Between 1980 and 1984 extensive studies were carried out in the Baltic Sea on trace metals (Cd, Co, Cu, Fe, Hg, Mn, Ni, Pb and Zn) in water, suspended matter and sediments. The results enabled the influence of different factors on metal distribution patterns to be considered. The vertical profiles of dissolved and particulate metals in waters of the central deep basins reflect influences caused by oxygen deficiency and anoxic conditions in near-bottom water layers. Peculiarities at Station BY15 in the Gotland Deep included high dissolved Fe, Mn and Co concentrations and remarkable enrichment of Zn (0.64%), Cd (51 μg g−1) and Cu (0.15%) in particulate matter from the anoxic zone. Manganese-rich particles were accumulated above this layer.In fine-grained soft sediments below anoxic deep waters, maximum contents of Cd, Cu and Zn were observed, relative to other coring sites, between Bothnian Bay and Lübeck Bight. The Hg content in sediments probably reflects the joint flocculation with organic matter. Land-based sources seem to play the leading part for maximum lead contents.  相似文献   

10.
Solid sediment, pore and epibenthic waters were collected from the Thau lagoon (France) in order to study the post-depositional partition and mobility of mercury in organic rich sediment. Total Hg (HgT) and monomethylmercury (MMHg) profiles were produced in both dissolved and solid phases. The distribution of HgT in the solid phase appeared to be related to the historical changes in the Hg inputs into the lagoon. HgT was in equilibrium between solid and solution phases in the sulfidic part of the cores, with a mean log Kd of 4.9 ± 0.2. The solid phase appeared to be a source of HgT for pore water in the upper oxic to suboxic parts of the cores. The MMHg represented a small fraction of HgT: 3–15% and 0.02–0.80% in the dissolved and solid phases, respectively. Its distribution was characterized by a main peak in the superficial sediments, and another deeper in the core within the sulfide-accumulating zone. In addition, high dissolved MMHg concentrations and methylated percentage were found in the epibenthic water. Ascorbate (pH 8) dissolution of the sediments and analyses of the soluble fraction suggest that the amorphous oxyhydroxides played a major role in controlling total and methylmercury mobility throughout the sediment–water interface. These features are discussed in terms of sources, transfer and transformations. Diffusive fluxes of HgT and MMHg from sediment to the water column for the warm period were estimated to be 40 ± 15 and 4 ± 2 pmol m−2 d−1, respectively.  相似文献   

11.
南沙珊瑚礁生态系中元素的垂直转移途径   总被引：4，自引：2，他引：2  
于１９９３年和１９９４年用沉积物捕捉器采集南沙永暑礁和渚碧礁内的沉降颗粒物,用中子活化法分析元素的含量并计算通量,通过对生源要素的统计相关分析,垂直沉降颗粒物中的元素人,非生源要素在泻湖中的停留时间的探讨,研究了南沙珊瑚礁生态系中元素的垂直转移途径,结果表明,在南沙珊胡礁泻湖中元素的停留时间较海水中短,元素的循环速率高,且尤以与生物作用有关的元素为甚;颗粒物中非生源要素的垂直转移主要是通过生物过程  相似文献   

12.
A six-month-long study was conducted of the fate of turbid river plumes from the Enipein watershed in Pohnpei, Federated States of Micronesia. Pohnpei is one of the wettest places on earth, with a mean annual rainfall exceeding 4 m in the lowlands and 8 m in the highlands. The river waters were clear of sediment except after major storms with rainfall exceeding 5 cm day−1. Following a storm, the river plume spread in the mangrove fringed estuary and in the coral reef lagoon. The waters were highly stratified in temperature, salinity, and suspended sediment concentration. The brackish water was flushed out in four days, while the suspended sediment all settled out in the estuary, in the mangroves, and in the lagoon including on the coral reefs, in less than one day. The mean rate of sedimentation exceeded 35 mg cm−2 d−1 both over the mangroves and on the adjacent coral reefs. While this leads to no detrimental effects on the mangroves, sediment smothers corals and leads to substantial coral mortality in the lagoon. The mud is not flushed out from the lagoon because there are no strong currents from waves or tides. This high sedimentation rate is attributable to poor farming and land-use practices on the upland areas.  相似文献   

13.
Dissolved organic nitrogen (DON), dissolved organic carbon (DOC) and inorganic nutrient concentrations were determined in samples from an area encompassing the Northeast Water Polynya from June to August 1993. In June, still ice-covered polynya area surface waters (PySW) had significantly higher (p<0.05) DOC concentrations (110 μM, n=68) than surface water outside the polynya area (96 μM, n=6). Melting ice and ice algae are suggested as DOC sources. DOC concentrations found in this study are consistent with other studies showing higher DOC concentrations in the Arctic than in other ocean areas. As the productive season progressed, DOC concentrations in Polynya surface water (PySW) decreased (p<0.05) from 110 to 105 μM, while DON concentrations increased (p<0.05) from 5.6 to 6.1 μM, causing a significant decrease (p<0.05) in the C : N ratios of DOM from spring (C : N ratio 20) to summer (C : N ratio 17). We found a significant (p<0.05) decrease in the DOM C : N ratio in all water masses within the polynya area as the productive season progressed. DON was the largest fraction of total dissolved nitrogen (TDN) in PySW and surface waters outside the polynya area. TDN was calculated as the sum of DON, nitrate, nitrite and ammonium concentrations. DON increased (p<0.05) from 62% to 73% of TDN in PySW from spring to summer, a result of increasing DON concentrations and decreasing inorganic nitrogen concentrations over the productive season. The seasonal accumulation of DON and the corresponding decrease in nitrate concentrations in waters with primary production indicate that it is important to take the DON pool into account when estimating export production from nitrate concentration decreases in surface waters. PySW TDN concentrations decreased (p<0.05) from 9.1 (n=61) to 8.6 μM (n=60) from spring (May 25 through June 19) to summer (July 1 through July 27). The seasonal decrease in surface water TDN concentrations corresponded to increases in TDN concentrations in deeper water masses within the Polynya. Most of the TDN increase in deep water was in the form of DON. A possible explanation is that PON was dissolved (partially remineralized) in the water column at mid depths, causing increases in the DON concentration. Transfer of N from PySW (with a short residence time in the polynya area) to Polynya Intermediate Water and deep waters of the Norske and Westwind Trough with multi-year residence times keeps N from leaving the polynya area. In spring, nutrients from degradation of OM in PyIW could support primary production. The role of PyIW as an OM trap could be important in supporting primary production in the polynya area.  相似文献   

14.
The Arcachon lagoon is a 156 km2 temperate mesotidal lagoon dominated by tidal flats (66% of the surface area). The methane (CH4) sources, sinks and fluxes were estimated from water and pore water concentrations, from chamber flux measurements at the sediment–air (low tide), sediment–water and water–air (high tide) interfaces, and from potential oxidation and production rate measurements in sediments. CH4 concentrations in waters were maximal (500–1000 nmol l−1) in river waters and in tidal creeks at low tide, and minimal in the lagoon at high tide (<50 nmol l−1). The major CH4 sources are continental waters and the tidal pumping of sediment pore waters at low tide. Methanogenesis occurred in the tidal flat sediments, in which pore water concentrations were relatively high (2.5–8.0 μmol l−1). Nevertheless, the sediment was a minor CH4 source for the water column and the atmosphere because of a high degree of anaerobic and aerobic CH4 oxidation in sediments. Atmospheric CH4 fluxes at high and low tide were low compared to freshwater wetlands. Temperate tidal lagoons appear to be very minor contributor of CH4 to global atmosphere and to open ocean.  相似文献   

15.
The complexation of dissolved Ni has been evaluated in a rapidly-flushed, rural estuary (Tweed, UK) by ligand exchange-adsorptive cathodic stripping voltammetry. Results suggest the presence of strongly binding ligands, L, throughout, with average stability constants of about 1019 and which are saturated by ambient Ni concentrations. Equilibrium speciation calculations incorporating these constants in WHAM, version 6, predict an increase in Ni complexation (as NiL) from about 50% of total dissolved Ni in fresh water to over 90% in sea water. Equivalent calculations using the default-mode fulvic and humic substances (FS and HS, respectively) encoded in the WHAM database predict a reduction in complexation (as NiFS + NiHS) from about 20% in fresh water to less than 1% in sea water. Discrepancies arising from the two approaches are largely attributed to the different analytical detection windows employed. Thus, a better representation of Ni complexation is derived from including both types of complexant in the speciation calculations, resulting in estimates of net complexation in excess of 60% of total dissolved Ni throughout the estuary. The uncertainties and assumptions inherent in all computations illustrate the difficulty in measuring or predicting metal complexation in estuaries.  相似文献   

16.
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   

17.
W. Balzer 《Marine Chemistry》1985,15(4):379-380
Representative profiles of inorganic nitrogenous species dissolved in interstitial waters of coral reef sands are presented. Ammonium is the dominant nitrogenous species in these pore waters with concentrations of up to 40 μm. Nitrate is present but in lower concentrations. Nitrite is found only occasionally in trace amounts. Computations of diffusive fluxes and inferences concerning microbial activity are derived from the profile structures. Computed flux rates of nitrogenous species from the sediment to the water column range between 0.75 and 1.37 μM m?1 h?1. These inputs may represent a significant source of recycled nitrogen to the primary producers of the coral reef ecosystem.  相似文献   

18.
Freshwater concentrations confirm the pristine character of the Lena River environment as already pointed-out in a previous study with a limited set of data (Martin et al., 1993). Total dissolved concentrations of the freshwater are 13.8 ± 1.6 nM, Cu, 4.4 ± 0.1 nM, Ni, 0.054 ± 0.047 nM, Cd, 642 ± 208 nM, Fe, 0.2–0.3 nM Pb and 1.2 ± 1.0 nM, Zn. For Zn and Pb, a simple mixing of the Lena River waters with the Arctic waters is observed. Relationships with salinity suggest that for Cu, Ni and Cd, there is a mobilization of the dissolved fraction from the suspended matter, with an increase of the dissolved concentration of 1.5, 3 and 6 times, respectively. For Fe, the total dissolved concentrations follow an exponential decrease in the mixing zone and 80% of the total “dissolved” Fe is removed from the solution. For Cu, Ni, Cd and Fe, the riverine end-members are 20 nM, 12 nM, 0.3 nM and 47 nM, respectively. When considering the input of total dissolved metals to the Arctic Ocean, the fraction attributed to the freshwaters from the Arctic rivers appears to be small (4% of the input of dissolved metal to the Arctic Ocean for Cd, 27% for Cu, 11 % for Ni and 2% for Zn). Metal concentrations in the Laptev Sea and Arctic Ocean are very similar, indicating a generally homogeneous distribution in the areas sampled.  相似文献   

19.
Elevated methane (CH4) concentrations (128–2692×103 nM) occur in the hypersaline anoxic brine pools of Bannock and Urania Basins, eastern Mediterranean Sea, compared to low concentrations (17–80×103 nM) in the sediments below the anoxic brines. The CH4 enrichment in the brines might be due to the long residence time of the brine in the Basin. An attempt is made to determine the sources for the enriched dissolved CH4 by considering the influence of hydrothermal activity, the occurrence of sapropel layers (biogenic) and dissolution of gas hydrates. Furthermore, it is suggested that the enriched CH4 in Bannock and Urania Basins is diffused and mixed with the overlying waters by local upward transport mechanisms that selectively move CH4 upward in these Basins.  相似文献   

20.
The role of coastal lagoons and estuaries as sources or sinks of inorganic carbon in upwelling areas has not been fully understood. During the months of May–July, 2005, we studied the dissolved inorganic carbon system in a coastal lagoon of northwestern Mexico during the strongest period of upwelling events. Along the bay, different scenarios were observed for the distributions of pH, dissolved inorganic carbon (DIC) and apparent oxygen utilization (AOU) as a result of different combinations of upwelling intensity and tidal amplitude. DIC concentrations in the outer part of the bay were controlled by mixing processes. At the inner part of the bay DIC was as low as 1800 μmol kg−1, most likely due to high water residence times and seagrass CO2 uptake. It is estimated that 85% of San Quintín Bay, at the oceanic end, acted as a source of CO2 to the atmosphere due to the inflow of CO2-rich upwelled waters from the neighboring ocean with high positive fluxes higher than 30 mmol C m−2 d−1. In contrast, there was a net uptake of CO2 and HCO3− by the seagrass bed Zostera marina in the inner part of the bay, so the pCO2 in this zone was below the equilibrium value and slightly negative CO2 fluxes of −6 mmol C m−2 d−1. Our positive NEP and ΔDIC values indicate that Bahía San Quintín was a net autotrophic system during the upwelling season during 2005.  相似文献   

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