首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 413 毫秒
1.
In this study, the CDOM absorption coefficient at 350 nm [aCDOM(350)] and CDOM excitation emission matrix (EEM) fluorescence were used to estimate annual fluxes of dissolved organic carbon (DOC) from the Cape Fear River to Long Bay in the South Atlantic Bight. Water samples were collected during a 3.5 year period, from October 2001 through March 2005, in the vicinity of the Cape Fear River (CFR) outlet and adjacent Onslow Bay (OB). Parallel factor analysis (PARAFAC) of CDOM EEM spectra identified six components: three terrestrial humic-like, one marine humic-like and two protein-like. Empirical relationships were derived from the PARAFAC model between DOC concentration and aCDOM(350), total fluorescence intensity and the intensities of respective EEM components. DOC concentration and CDOM optical parameters were very well correlated and R2 values ranged from 0.77 to 0.90. Regression analyses revealed that the non-absorbing DOC fraction, in DOC concentration estimated from CDOM optical parameters, varied with the qualitative composition of the CDOM. DOC concentration and intensity of the humic-like CDOM components characterized by excitation maxima at longer wavelengths have significantly higher estimated non-absorbing DOC compared to the analogous relationships between DOC and intensity of the humic-like CDOM components characterized by excitation maxima at shorter wavelengths. The relationships between DOC concentration and intensity of one of the protein-like components resulted in significantly reduced non-absorbing DOC fraction in DOC concentration estimation. Results of regression analyses between fluorescence intensities of specific EEM components and CDOM-specific absorption coefficients suggest that the relative proportion of humic-like CDOM components (characterized by excitation maximum at longer wavelengths) and the main protein-like component have the most impact on the values of a?CDOM(350). Based on the relationships between aCDOM(350), Cape Fear River flow, and DOC concentrations, DOC fluxes were estimated for 2002, 2003 and 2004. DOC fluxes varied from 1.5 to 6.2 × 1010 g C yr? 1, depending on river flow.  相似文献   

2.
Detailed vertical profiles of dissolved organic carbon (DOC), nitrogen (DON) and DOC/DON ratios in the Australian sector of the Southern Ocean (56°–65°S around 140°W transect) were obtained by a high-temperature catalytic oxidation method with a modified Shimadzu TOC-5000 unit. The simultaneous analyses of DOC and total dissolved nitrogen (TDN) gave high precision results (±0.7 μMC and ±0.3 μMN). In surface layers, DOC concentrations were lower (45–55 μM) than those generally obtained from other oceanic environments (60–90 μM). The surface concentrations of DON varied from 4 to 9 μM, but within the range generally reported for other ocean regions. Surface excesses of DOC and DON were calculated against nearly constant subsurface concentrations. A consistent contribution of low C/N ratio (2.7–5.0) was found in the mid-surface layer (30–75 m), suggesting more extensive degradation of carbon-enriched materials and/or enhanced supply of nitrogen-enriched ones.  相似文献   

3.
The distribution of dissolved organic carbon (DOC) and nitrogen (DON) and particulate organic carbon (POC) and nitrogen (PON) was studied on a transect perpendicular to the Catalan coast in the NW Mediterranean in June 1995. The transect covered a hydrographically diverse zone, including coastal waters and two frontal structures (the Catalan and the Balear fronts). The cruise was conducted during the stratified period, characterized by inorganic nutrient depletion in the photic zone and a well established deep chlorophyll a maximum. DOC concentrations were measured using a high-temperature catalytic oxidation method, and DON was determined directly, with an update of the Kjeldahl method, after removal of inorganic nitrogen.The ranges of DOC and DON concentrations were 44–95 μM-C and 2.8–6.2 μM-N. The particulate organic matter ranged between 0.9 and 14.9 μM-C and from 0.1 to 1.7 μM-N. The DOC : DON molar ratio averaged 15.5±0.4, and the mean POC : PON ratio was 8.6±0.6. The distribution of dissolved organic matter (DOM) was inverse to that of the salinity. The highest concentrations of DOM were found in coastal waters and in the stations affected by the Catalan front, located at the continental shelf break.It was estimated that recalcitrant DOM constituted 67% of the DOM pool in the upper 50 m. The data suggest that accumulation of DOC due to the decoupling of production and consumption may occur in the NW Mediterranean during stratification and that the organic matter exported from the photic layer is dominated by C-rich material.  相似文献   

4.
The distribution and optical absorption characteristics of chromophoric dissolved organic matter (CDOM) were systematically investigated along three meridional transects in the North Atlantic Ocean and Caribbean Sea conducted as part of the 2003 US CLIVAR/CO2 Repeat Hydrography survey. Hydrographic transects covered in aggregate a latitudinal range of 5° to 62° north along longitudes 20°W (line A16N, Leg 1), 52°W (A20), and 66°W (A22). Absorption spectra of filtered seawater samples were collected and analyzed for depths ranging from the surface to ∼6000 m, sampling all the ocean water masses in the western basin of the subtropical North Atlantic and several stations on the North and South American continental slopes. The lowest surface abundances of CDOM (< 0.1 m−1 absorption coefficient at 325 nm) were found in the central subtropical gyres while the highest surface abundances (∼0.7 m−1) were found along the continental shelves and within the subpolar gyre, confirming recent satellite-based assessments of surface CDOM distribution. Within the ocean interior, CDOM abundances were relatively high (0.1–0.2 m−1 absorption coefficient at 325 nm) except in the subtropical mode water, where a local minimum exists due to the subduction of low CDOM surface waters during mode water formation. In the subthermocline water masses of the western basin, changes in CDOM abundance are not correlated with increasing ventilation age as assessed using chlorofluorocarbon (CFC) concentrations and the atmospheric CFC history. But dissolved organic carbon (DOC) mass-specific absorption coefficients of CDOM increase with increasing ventilation age in the deep sea, indicating that CDOM is a refractory component of the DOC pool. The overall CDOM distribution in the North Atlantic reflects the rapid advection and mixing processes of the basin and demonstrates that remineralization in the ocean interior is not a significant sink for CDOM. This supports the potential of CDOM as a tracer of ocean circulation processes for subducted water masses.  相似文献   

5.
Apparent oxygen utilization (AOU), dissolved organic carbon (DOC), coloured dissolved organic matter (CDOM) absorption spectra, and CDOM fluorescence characteristic of aromatic amino acids (excitation/emission 280 nm/320 nm; F(280/320)) and marine-humic like substances (320 nm/410 nm; F(320/410)) were measured in full depth during a cruise in the temperate Eastern North Atlantic (ENA). An optimum multi-parameter (OMP) inverse method was run to calculate water mass proportion-weighted average (archetypal) concentrations of these chemical parameters for all water masses and samples. Archetypal concentrations retain the variability due to water mass mixing and basin scale mineralization from the water mass formation sites to the study area. Conversely, the difference between measured and archetypal concentrations, retain the variability due to dissimilarities in mineralization processes within the study area. Our analysis indicates that DOC supported 26±3% of the AOU in the dark temperate ENA and that basin scale processes occurring at and from the formation area of the water masses explained 63% of the total DOC variability. Our data also suggests that DOC remineralized at the basin scale was of lower molecular weight, and with a lower proportion of fluorescent aromatic amino acids than found within the study area. The relationship between the absorption coefficient at 254 nm (aCDOM(254)) and AOU indicates that aCDOM(254) was consumed during organic matter remineralization in the dark ocean, with 55% of the variability being explained by basin scale processes. The relationships of F(320/410) with AOU and DOC confirmed that marine humic-like substances are produced by microbial degradation processes, at a rate of 6.1±0.9×10−3 mg equivalents of QS mol AOU−1. Our results also indicate that basin-scale remineralization processes account for 85% of the total variability of F(320/410), emphasizing that large scale processes control the formation of humic-like substance in the dark ENA.  相似文献   

6.
To assess the magnitude, distribution and fate of net community production (NCP) in the Chukchi Sea, dissolved inorganic carbon (DIC), dissolved organic carbon (DOC) and dissolved organic nitrogen (DON), and particulate organic carbon (POC) and particulate organic nitrogen (PON) were measured during the spring and summer of 2004 and compared to similar observations taken in 2002. Distinctive differences in hydrographic conditions were observed between these two years, allowing us to consider several factors that could impact NCP and carbon cycling in both the Chukchi Shelf and the adjacent Canada Basin. Between the spring and summer cruises high rates of phytoplankton production over the Chukchi shelf resulted in a significant drawdown of DIC in the mixed layer and the associated production of DOC/N and POC/N. As in 2002, the highest rates of NCP occurred over the northeastern part of the Chukchi shelf near the head of Barrow Canyon, which has historically been a hotspot for biological activity in the region. However, in 2004, rates of NCP over most of the northeastern shelf were similar and in some cases higher than rates observed in 2002. This was unexpected due to a greater influence of low-nutrient waters from the Alaskan Coastal Current in 2004, which should have suppressed rates of NCP compared to 2002. Between spring and summer of 2004, normalized concentrations of DIC in the mixed layer decreased by as much as 280 μmol kg−1, while DOC and DON increased by ∼16 and 9 μmol kg−1, respectively. Given the decreased availability of inorganic nutrients in 2004, rates of NCP could be attributed to increased light penetration, which may have allowed phytoplankton to increase utilization of nutrients deeper in the water column. In addition, there was a rapid and extensive retreat of the ice cover in summer 2004 with warmer temperatures in the mixed layer that could have enhanced NCP. Estimates of NCP near the head of Barrow Canyon in 2004 were ∼1500 mg carbon (C) m−2 d−1 which was ∼400 mg C m−2 d−1 higher than the same location in 2002. Estimates of NCP over the shelf-break and deep Canada Basin were low in both years, confirming that there is little primary production in the interior of the western Arctic Ocean due to near-zero concentrations of inorganic nitrate in the mixed layer.  相似文献   

7.
Recent efforts to construct global ocean budgets for carbon have recognized the importance of continental margins. In this study, we constructed budgets for the Strait of Georgia, a temperate, North American west coast basin that receives the inflow of one of the world's major rivers. Drawing from published and unpublished data, we have estimated the magnitude of the various sources and sinks of fresh water, sediment and organic carbon.The Fraser River is the dominant source of fresh water and particles to the strait, contributing approximately 73% of the 158×109 m3 year−1 of water and 64% of the 30×109 kg year−1 of particles. Other rivers supply most of the remainder, while rain, groundwater and anthropogenic sources of water and particles are negligible in comparison. Fresh water escapes the Strait of Georgia through Juan de Fuca Strait, but particulate inputs are approximately balanced by sedimentation within the greater Strait of Georgia, implying almost complete trapping of particles.Dissolved and particulate organic carbon are derived mainly from in situ primary production (855×106 kg year−1) and from the Fraser River (550×106 kg year−1). Other rivers contribute 200×106 kg year−1 of organic carbon, and anthropogenic sources (ocean dumping, sewage, pulp mills and aquaculture) a further 119×106 kg year−1. Particulate organic carbon is predominantly buried (428×106 kg year−1) or oxidized (90×106 kg year−1) in the sediments of the strait. About 70% of the organic carbon that enters or is produced in the strait is dissolved. Most of the dissolved organic carbon is oxidized within the strait (784×106 kg year−1), but the remainder (400×106 kg year−1) is exported to the Pacific Ocean. Although the particulate organic carbon budget by itself implies net autotrophy, dissolved organic carbon oxidation may make the Strait of Georgia slightly net heterotrophic.  相似文献   

8.
《Marine Chemistry》2007,103(1-2):131-145
We have investigated submarine groundwater discharge to Nueces Bay (Texas) using naturally occurring Ra isotopes. Dissolved Ra activities in Nueces Bay are among the highest observed in coastal estuaries; as great as 2600 dpm m− 3 for 228Ra and 1000 dpm m− 3 for 226Ra. Using a combination of salt and Ra mass balances, we demonstrate that river discharge and bay bottom sediments cannot supply the Ra needed to balance tidal export. In the case of 226Ra there is an additional source of 218 × 106 ± 105% dpm day− 1 which is 9 times the maximum supply from bay bottom sediments and 50 times the Ra supplied by the Nueces River. A groundwater flux of 310,000 m3 day− 1 is required to supply the needed 226Ra, based on the measured maximum Ra activity of local groundwater. Though as little as 10% of this flux may be advecting terrestrial groundwater this would still represent 160% of the Nueces River discharge. This makes it unlikely that groundwater discharge alone is supplying all of the additional 226Ra. Oil-field brine could potentially account for the remainder. Leakage of 6290 m3 day− 1 of oil-field brine from the submerged petroleum wells and pipelines within the bay could supply all of the needed 226Ra. Such large fluxes of brackish groundwater and oil-field brine could significantly affect bay nitrogen budgets, salinities, and dissolved oxygen concentrations and should be considered when determining the freshwater inflow requirements for Nueces Bay and similar estuaries.  相似文献   

9.
We examined the contribution of submarine groundwater discharge (SGD) to nutrient budgets in Hwasun Bay, Jeju Island, Korea in August 2009, October 2014, and May 2015. The concentrations of dissolved inorganic nitrogen (DIN) and dissolved inorganic phosphorus (DIP) in fresh groundwater were in the range of 285?716 μM and 2.3?3.2 μM, respectively, which were each 1?2 orders of magnitude higher than those in the bay seawater. The outer-bay seawater flowing into the bay was oligotrophic (2.9 ± 1.9 μM for DIN and 0.2 ± 0.3 μM for DIP). Nutrient budget calculations were performed for each season by accounting for submarine fresh groundwater discharge (SFGD) and water residence times. In August 2009 (DIN = 1.8 μM and DIN:DIP ratio = 4.6 for the outerbay water), DIN inputs from SFGD accounted for approximately 40% of the DIN inventory in the bay seawater. In October 2014 (DIN = 1.1 μM and DIP < 0.05 μM for the outer-bay water), DIP from SFGD accounted for approximately 100% of the DIP inventory in the bay seawater. In May 2015, mean concentrations of DIN and DIP in the bay seawater were 8.6 ± 12 μM and 0.11 ± 0.04 μM, respectively, with conservative behaviors in the bay seawater in association with excessive groundwater inputs. These results imply that SGD plays a critical but different role in nutrient budgets and stoichiometry in coastal waters off a volcanic island depending on open-ocean nutrient conditions.  相似文献   

10.
Nutrient inputs associated with coastal population growth threaten the integrity of coastal ecosystems around the globe. In order to assess the threat posed by rapid growth in tourism, we analyzed the nutrient concentrations as well as the δ15N of NO3− and macrophytes to detect wastewater nitrogen (N) at 6 locations along a groundwater-dominated coastal seagrass bed on the Caribbean coast of Mexico. We predicted that locations with greater coastal development would have higher concentrations of dissolved inorganic nitrogen (DIN) and phosphorus (P), as well as δ15N of NO3−, reflecting wastewater sources of N. However, concentrations of NO3− were not significantly different between developed (3.3 ± 5.3 μM NO3−) and undeveloped (1.1 ± 0.7 μM) marine embayments. The most important control on DIN concentration appeared to be mixing of fresh and salt water, with DIN concentrations negatively correlated with salinity. The δ15N of NO3− was elevated at an inland pond (7.0 ± 0.42‰) and a hydrologically-connected tide pool (7.6 ± 0.57‰) approximately 1 km downstream of the pond. The elevated δ15N of NO3− at the pond was paralleled by high δ15N values of Cladophora sp., a ubiquitous green alga (10 ± 1‰). We hypothesize that inputs of nitrogen rich (NO3− > 30 μM) groundwater, characterized by 15N enriched signatures, flow through localized submarine groundwater discharges (SGD) and contribute to the elevated δ15N signatures observed in many benthic macrophytes. However, changes in nitrogen concentrations and isotope values over the salinity gradient suggest that other processes (e.g. denitrification) could also be contributing to the 15N enrichments observed in primary producers. More measurements are needed to determine the relative importance of nitrogen transformation processes as a source of 15N to groundwaters; however, it is clear that continued inputs of anthropogenic N via SGD have the potential to severely impact ecologically and economically valuable seagrass meadows and coral reefs along the Caribbean coast of Mexico.  相似文献   

11.
One indicator of health in estuarine and coastal ecosystems is the ability of local waters to transmit sunlight to planktonic, macrophytic, and other submerged vegetation for photosynthesis. The concentration of coloured dissolved organic matter (CDOM) is a primary factor affecting the absorption of incident sunlight in coastal and estuarine waters. In estuaries, CDOM concentrations vary due to changes in salinity gradients, inflows of industrial and domestic effluents, and the production of new dissolved organic matter from marine biologic activity. CDOM absorption data have been collected from a variety of waters. However, there are a limited number of measurements along the US east coast and a general lack of data from New England waters.This study characterized the temporal and spatial variability of CDOM absorption over an annual cycle in Narragansett Bay and Block Island Sound (Rhode Island). Results suggested that, in Narragansett Bay, the magnitude of CDOM absorption is related to the seasonal variability of freshwater input from surrounding watersheds and new CDOM production from in situ biologic activity. The data show that the average CDOM absorption coefficient at 412 nm was 0·45 m−1 and the average spectral slope was 0·020 nm−1.  相似文献   

12.
The total organic carbon (TOC) and total inorganic carbon (CT) exchange between the Atlantic Ocean and the Mediterranean Sea was studied in the Strait of Gibraltar in September 1997. Samples were taken at eight stations from western and eastern entrances of the Strait and at the middle of the Strait (Tarifa Narrows). TOC was analyzed by a high-temperature catalytic oxidation method, and CT was calculated from alkalinity–pHT pairs and appropriate thermodynamic relationships. The results are used in a two-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, the Mediterranean outflow and the interface layer in between. Our observations show a decrease of TOC and an increase of CT concentrations from the surface to the bottom: 71–132 μM C and 2068–2150 μmol kg−1 in the Surface Atlantic Water, 74–95 μM C and 2119–2148 μmol kg−1 in the North Atlantic Central Water, 63–116 μM C and 2123–2312 μmol kg−1 in the interface layer, and 61–78 μM C and 2307–2325 μmol kg−1 in the Mediterranean waters. However, within the Mediterranean outflow, we found that the concentrations of carbon were higher at the western side of the Strait (75–78 μM C, 2068–2318 μmol kg−1) than at the eastern side (61–69 μM C, 2082–2324 μmol kg−1). This difference is due to the mixing between the Atlantic inflow and the Mediterranean outflow on the west of the Strait, which results in a flux of organic carbon from the inflow to the outflow and an opposite flux of inorganic carbon. We estimate that the TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from (0.97±0.8)104 to (1.81±0.90)104 mol C s−1 (0.3×1012 to 0.56×1012 mol C yr−1), while outflow of inorganic carbon ranges from (12.5±0.4)104 to (15.6±0.4)104 mol C s−1 (3.99–4.90×1012 mol C yr−1). The high variability of carbon exchange within the Strait is due to the variability of vertical mixing between inflow and outflow along the Strait. The prevalence of organic carbon inflow and inorganic carbon outflow shows the Mediterranean Sea to be a basin of active remineralization of organic material.  相似文献   

13.
The fate of terrigenous dissolved organic carbon (tDOC) delivered to the Arctic Ocean by rivers remains poorly constrained on both spatial and temporal scales. Early reports suggested Arctic tDOC was refractory to degradation, while recent studies have shown tDOC removal to be an active but slow process. Here we present observations of DOC, salinity, δ18O, and 228Ra/226Ra in the Polar Surface Layer (PSL) over the outer East Siberian/Chukchi shelf and the adjacent Makarov and Eurasian basins of the eastern Arctic Ocean. This off-shelf system receives meteoric water, introduced by rivers, after a few years residence on the shelf. Elevated concentrations of DOC (> 120 μM C) were observed in low salinity (~ 27) water over the Makarov Basin, suggesting inputs of tDOC-enriched river water to the source waters of the Transpolar Drift. The regression of DOC against salinity indicated an apparent tDOC concentration of 315 ± 7 μM C in the river water fraction, which is significantly lower than the estimated DOC concentration in the riverine sources to the region (724 ± 55 μM C). To obtain the timescale of removal, estimates of shelf residence were coupled with measurements of dissolved 228Ra/226Ra, an isotopic tracer of time since shelf residence. Shelf residence time coupled with DOC distributions indicates a first order tDOC removal rate constant, λ = 0.24 ± 0.07 yr-1, for the eastern Arctic, 2.5–4 times higher than rates previously observed in the western Arctic. The observed removal of tDOC in the eastern Arctic occurs over the expansive shelf area, highlighting the initial lability of tDOC upon delivery to the Arctic Ocean, and suggests that tDOC is composed of multiple compartments defined by reactivity. The relatively rapid remineralization of tDOC on the shelves may mitigate the strength of the Arctic Ocean atmospheric CO2 sink if a projected increase in labile tDOC flux occurs.  相似文献   

14.
The biogeochemistry and magnitude of submarine groundwater discharge (SGD) was investigated in one of the largest tidal flat ecosystems worldwide, along the Yellow Sea coast. A representative semi-enclosed embayment located in the south eastern Yellow Sea, Hampyeong Bay, was chosen for this purpose. Groundwater and seawater samples were collected in three seasons (May, July, and September) and analyzed for Ra isotopes, nutrients, and photosynthetic pigments. The biogeochemistry of SGD was strongly influenced by tidal oscillations and seasonal precipitation changes and switched from a brackish, nutrient-enriched regime in May and July to an exclusively saline regime, with lower nutrient concentrations, in September. SGD magnitudes, calculated by using a 226Ra mass balance model, were 0.14 m3 m? 2 d? 1 in May and 0.35 m3 m? 2 d? 1 in September. A nutrient mass balance was established for the two campaigns, which suggests that SGD causes the flushing of substantial amounts of pore water nutrients into this embayment; because of SGD, the embayment acts as a source of dissolved inorganic silicates (DSi) that are transported to the open ocean. Potential C fixation rates derived from this nutrient mass balance were compared with two different models for water-column phytoplankton productivity based on water-column Chl a and local irradiation levels. The Chl a-based models generally showed lower C fixation rates than the nutrient-based mass balance, indicating removal of up to 70% of the nutrients by other primary producers, such as benthic algae. During monsoon season, when benthic algal biomass is high and nutrient fluxes are substantial due to a terrestrial component, SGD — driven benthic primary production could play a significant role in this large tidal flat ecosystem.  相似文献   

15.
The first carbon budget constructed for the Barents Sea to study the fluxes of carbon into, out of, and within the region is presented. The budget is based on modelled volume flows, measured dissolved inorganic carbon (DIC) concentration, and literature values for dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations. The results of the budget show that ～5600±660×106 t C yr?1 is exchanged through the boundaries of the Barents Sea. If a 40% uncertainty in the volume flows is included in the error calculation it resulted in a total uncertainty of ±1600×106 t C yr?1. The largest part of the total budget flux consists of DIC advection (～95% of the inflow and ～97% of the outflow). The other sources and sinks are, in order of importance, advection of organic carbon (DOC+POC; ～3% of both in- and outflow), total uptake of atmospheric CO2 (～1% of the inflow), river and land sources (～0.2% of the inflow), and burial of organic carbon in the sediments (～0.2% of the outflow). The Barents Sea is a net exporter of carbon to the Arctic Ocean; the net DIC export is ～2500±660×106 t C yr?1 of which ～1700±650×106 t C yr?1 (～70%) is in subsurface water masses and thus sequestered from the atmosphere. The net total organic carbon export to the Arctic Ocean is ～80±20×106 t C yr?1. Shelf pumping in the Barents Sea results in an uptake of ～22±11×106 t C yr?1 from the atmosphere which is exported out of the area in the dense modified Atlantic Waters. The main part of this carbon was channelled through export production (～16±10×106 t C yr?1).  相似文献   

16.
海底地下水排放对典型红树林蓝碳收支的影响   总被引：1，自引：0，他引：1  
海底地下水排放(Submarine Groundwater Discharge，SGD)是陆海相互作用的重要表现形式之一，其携带的物质对近岸海域生源要素的收支有重要影响。本文利用222Rn示踪技术估算了我国典型红树林海湾—广西珍珠湾在2019年枯季(1月)SGD携带的碳通量。调查发现，地下水中222Rn活度、溶解无机碳(DIC)和溶解有机碳(DOC)的平均浓度均高于河水和湾内表层海水。利用222Rn质量平衡模型估算得到珍珠湾SGD速率为(0.36±0.36) m/d，SGD输入到珍珠湾的DIC和DOC通量分别为(2.41±2.63)×107 mol/d和(1.96±2.20)×106 mol/d。珍珠湾溶解碳的源汇收支表明，SGD携带的DIC和DOC分别占珍珠湾总DIC和总DOC来源的91%和89%。因此，SGD携带的DIC和DOC是珍珠湾DIC和DOC的主要来源，是海岸带蓝碳收支和生物地球化学循环过程中的重要组成。  相似文献   

17.
Marginal seas provide a globally important interface between land and interior ocean where organic carbon is metabolized, buried or exported. The trophic status of these seas varies seasonally, depending on river flow, primary production, the proportion of dissolved to particulate organic carbon and other factors. In the Strait of Georgia, about 80% of the organic carbon in the water column is dissolved. Organic carbon enters at the surface, with river discharge and primary production, particularly during spring and summer. The amount of organic carbon passing through the Strait (∼16 × 108 kg C yr−1) is almost twice the standing inventory (∼9.4 × 108 kg C). The organic carbon that is oxidized within the Strait (∼5.6 × 108 kg yr−1) presumably supports microbial food webs or participates in chemical or photochemical reactions, while that which is exported (7.2 × 108 kg yr−1) represents a local source of organic carbon to the open ocean.  相似文献   

18.
Carbon overconsumption, i.e. the consumption of inorganic carbon relative to inorganic nitrogen in excess of the Redfield ratio at the sea surface, was examined in relation to the dynamics of dissolved organic carbon and nitrogen (DOC and DON) in the northeast Atlantic. We observed the presence of N-poor dissolved organic matter (DOM) in surface water during summer, requiring the consumption of inorganic carbon and nitrogen in a ratio exceeding the Redfield ratio. The C : N ratio of bulk DOM is not only different from the Redfield ratio but also variable, i.e. no fixed conversion factor of C and N exists where DOM is important in C and N transformations. The existence of N-poor DOM is recognized as a feature typical of oligotrophic systems. At the same time, the C : N ratios of particles conform to Redfield stoichiometry as does deep-ocean chemistry. The implications of this finding are discussed, the conclusion being that, while DOM buildup contributes to CO2 drawdown seasonally, its impact on long-term carbon and nitrogen balance of the ocean is small.  相似文献   

19.
The variation of dissolved organic matter (DOM) and fluorescence characteristics during the phytoplankton bloom were investigated in Yashima Bay, at the eastern part of the Seto Inland Sea, Japan. We found significant accumulations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), chromophoric dissolved organic matter (CDOM) fluorescence, and UV260 during the phytoplankton bloom period in 2005, although lower accumulations of DOC and DON and only increases of CDOM fluorescence were observed during the bloom period in 2006. Little or no correlation between DOM and phytoplankton abundance might be due to the composition of DOM, which is a complex mixture of organic materials. The 3D-EEM results revealed that the DOM produced around the phytoplankton bloom period contained tyrosine, tryptophan, and humic-like substances. Our results showed that the occurrence of phytoplankton bloom contributed to the production of DOM in coastal water but the DOM accumulation depended on the type of phytoplankton bloom, the phytoplankton species in particular. From our results, we concluded that phytoplankton have a great role in the dynamics of DOM as a producer in a coastal environment.  相似文献   

20.
Measurements of nitrate and ammonium in precipitation and associated with aerosols were conducted at Rutgers University Marine Field Station in Tuckerton, New Jersey from March 2004 to March 2005 to characterize atmospheric nitrogen deposition to the Mullica River-Great Bay Estuary. The arithmetic means of nitrate and ammonium concentrations for precipitation samples were 2.3 mg L−1 and 0.42 mg L−1, respectively. Nitrate and ammonium concentrations in aerosol samples averaged 3.7 μg m−3 and 1.6 μg m−3, respectively. Wet deposition rates appeared to vary with season; the highest rate of inorganic nitrogen deposition (nitrate + ammonium) occurred in the spring with an average value of 1.33 kg-N ha−2 month−1. On an annual basis, the total (wet and dry) direct atmospheric deposition fluxes into the Mullica River-Great Bay Estuary were 7.08 kg-N ha−2 year−1 for nitrate and 4.44 kg-N ha−2 year−1 for ammonium. The total atmospheric inorganic nitrogen directly deposited to the Mullica River-Great Bay Estuary was estimated to be 4.79 × 104 kg-N year−1, and the total atmospheric inorganic nitrogen deposited to the Mullica River watershed was estimated to be 1.69 × 106 kg-N year−1. Only a fraction of the nitrogen deposited on the watershed will actually reach the estuary; most of the nitrogen will be retained in the watershed due to utilization and denitrification during transport. The amount of N reaching the Mullica River-Great Bay Estuary indirectly is estimated to be 5.07 × 104 kg-N year−1, approximately 97% is retained within the watershed. This atmospheric nitrogen deposition may stimulate phytoplankton productivity in the Mullica River-Great Bay ecosystem.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号