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1.
Chemical speciation of particulate metals in seawater was examined theoretically. Mass balance considerations showed that the apparent conditional stability constant, defined for organically binding metals in suspended particles, coincides with the conditional stability constant determined for the corresponding metal-organic complexes dissolved in seawater. This hypothesis suggests that some metals, which are present as organic complexes (e.g. copper), are directly associated with particulate organic matter. Metals, whose free ion is buffered by organic and/or inorganic ligands, may be used as indicators of the presence of particulate organic matter in the marine environment.  相似文献   

2.
Speciation of copper and nickel in the water phase of incubated marine slurries under aerobic conditions was performed with MnO2 and Sep—Pak C18 cartridges. Changes in time during the incubations of concentrations of dissolved organic carbon (DOC), dissolved copper and nickel and inorganic nitrogen were followed. The influence of organic complexation on the dissolved concentrations of copper and nickel was investigated as well as competition between copper and nickel for dissolved organic ligands.Two pools of dissolved organic ligands could be distinguished. With the MnO2 method a relatively strong ligand group was determined that was subjected to degradation. The conditional stability constant for copper with the relatively strong ligand was 1011.1. The conditional stability constant for the relatively strong nickel ligand was difficult to determine due to saturation of the ligand sites; it was found to be around 1010. However, it could not be ascertained whether nickel was reversibly com-plexed with the organic ligands.With Sep—Pak a relatively weak Hgand group was detected that was probably more resistant to degradation. The conditional stability constant of the weaker ligand could not be estimated, an approximation revealed that it was weaker than the ligand group determined with the MnO2 method. For copper the difference between binding strength of the ligand groups was at least 100, for nickel the difference was less.Competition between copper and nickel for the ligands could not be detected. Only during the first day of the experiment, when the system was not in equilibrium was competition suspected. However, the replacement of nickel by copper from the ligand sites was not straightforward and could not be accounted for by our model.The concentration of total dissolved copper during the first week of the experiment was found to be controlled on the one hand by release from the sediment of copper already associated with dissolved organic matter (DOM) and on the other hand by concentration of the strongest ligand. The calculated free copper concentration increased from 10−12 to 10−9mol l−1 due to the oxidation of the strongest ligand. After saturation of the strongest ligand the relatively weak ligand controlled the free copper concentration. A continuing release of copper from the sediment by degradation of particulate organic matter (POM) will not increase the free copper concentration until the ligand sites of the weaker ligands get saturated.The total dissolved nickel concentration seemed only to be determined by the sum of the concentrations of the organic ligands. A degradation of ligands resulted in a decrease of the total dissolved nickel concentration. The calculated free nickel concentration did not change with time.  相似文献   

3.
To clarify the nature of organic metal complexes dissolved in seawater, a ligand exchange reaction between ligands of natural origin and an aminopolycarboxylic acid (EDTA) was used to determine the conditional stability constants of organic metal complexes. The results indicate that more than two organic molecules complexed with copper and zinc exist in surface seawater. It is found that the conditional stability constants of these naturally-occurring organic metal complexes are 1–3 orders of magnitude higher than those of EDTA-Cu and EDTA-Zn complexes. These estimates of the conditional stability constants for the dominant species of organic copper and zinc complexes are 1011.8 and 109.3, respectively, at pH 8.1. The results indicate that these naturally-occurring organic metal complexes are stable species and not easily dissociated or displaced with others in the marine environment.  相似文献   

4.
The chemical speciation of dissolved mercury in surface waters of Galveston Bay was determined using the concentrations of mercury-complexing ligands and conditional stability constants of mercury-ligand complexes. Two classes of natural ligands associated with dissolved organic matter were determined by a competitive ligand exchange-solvent solvent extraction (CLE-SSE) method: a strong class (Ls), ranging from 19 to 93 pM with an average conditional stability constant (KHgLs) of 1028, and a weak class (Lw) ranging from 1.4 to 9.8 nM with an average KHgLs of 1023. The range of conditional stability constants between mercury and natural ligands suggested that sulfides and thiolates are important binding sites for dissolved mercury in estuarine waters. A positive correlation between the estuarine distribution of dissolved glutathione and that of mercury-complexing ligands supported this suggestion. Thermodynamic equilibrium modeling using stability constants for HgL, HgClx, Hg(OH)x, and HgCl(OH) and concentrations of each ligand demonstrated that almost all of the dissolved mercury (> 99%) in Galveston Bay was complexed by natural ligands associated with dissolved organic matter. The importance of low concentrations of high-affinity ligands that may originate in the biological system (i.e., glutathione and phytochelatin) suggests that the greater portion of bulk dissolved organic matter may not be important for mercury complexation in estuarine surface waters.  相似文献   

5.
An improved method for the direct determination of organic carbon in calcareous marine sediments, organisms and particulate matter is described. Samples are dissolved in phosphoric acid to remove carbonates, purged with oxygen to remove CO2, and the resulting acidic solution is analysed for total (dissolved and particulate) organic carbon. The method is rapid, involves minimal sample manipulation, and is both accurate (better than ± 2%) and precise (better than ± 0.2 mg organic carbon/g sediment). The method is especially suitable for modern carbonate sediments which have low levels of predominantly acid-soluble organic carbon.  相似文献   

6.
The phase partitioning of 234Th between dissolved (<10-kiloDalton, kD), colloidal (10 kD—0.4 μm), and particulate (⩾0.5 μm) matter across a horizontal transect, from a coastal station to the deep Canada Basin, and a vertical profile in the deep Canada Basin of the western Arctic Ocean was investigated. Concentrations of suspended particulate matter (SPM), dissolved, colloidal and particulate organic carbon, particulate organic nitrogen and nutrients (silicate, phosphate and nitrate) were also measured to assess transport and scavenging processes.Total 234Th (colloidal+particulate+dissolved) indicated deficiencies relative to secular equilibrium with its parent, 238U in the upper 100 m, which suggests active scavenging of 234Th onto particle surfaces. In contrast, at depths >200 m, general equilibrium existed between total 234Th and 238U. The inventory of SPM and the specific activity of particulate 234Th in the Canada Basin was about an order of magnitude higher than the profile reported for the Alpha Ridge ice camp station. This higher concentration of SPM in the southwestern Canada Basin is likely derived from ice-rafted sedimentary particles. Inventories of nutrients, and dissolved organic carbon and nitrogen in the upper 100 m of the Canada Basin are comparable to the other estimates for the central Arctic Ocean. Comparison of the mass concentrations of colloidal and filter-retained particulate matter as well as the activity of 234Th in these phases indicates that only a very small component of the colloidal material is actively involved in Th scavenging. Lower values of the conditional partition coefficient between the colloidal and dissolved phase indicate that the Arctic colloids are less reactive than colloidal material from other regions. The conditional partition coefficient between the filter-retained and dissolved phases (Kf) is generally higher than that for other regions, which is attributed to the higher complexation capacity of glacio-marine sedimentary particles in these waters. The 234Th-derived export of POC for the shelf and deep Canada Basin ranges between 5.6 and 6.5 mmol m−2 d−1, and is in agreement with other estimates reported for the central Arctic Ocean and Beaufort Sea.  相似文献   

7.
海洋沉积物/颗粒物是生源要素循环过程中的关键源与汇，沉积物/颗粒物一方面是海水生源要素的主要归宿，生源要素从溶解态经复杂的生物-化学过程转变为颗粒态，颗粒物质再沉降形成沉积物，另一方面，海洋沉积物/颗粒物经过微生物-浮游动物-底栖生物作用分解形成溶解态的生源要素，并释放到海水中再次被浮游植物利用，进入下一轮循环，所以，海洋沉积物/颗粒物具有异常重要的生态学功能。浮游植物是海水溶解态生源要素的利用者和海源颗粒态生源要素的初始形成者，浮游动物通过摄食浮游植物或其他有机颗粒物可释放出溶解态生源要素或形成更大的颗粒物，颗粒物沉降后形成的沉积物又通过底栖生物摄食-扰动-破碎等过程将颗粒生源要素释放进入水体参与再循环。生态系统不同类群的生物在颗粒生源要素的释放-沉降中所起的作用不同而又相互关联，其中浮游动物-底栖生物的摄食与代谢、微生物参与的分解过程起着非常重要的作用。所以，海洋沉积物/颗粒物生态学功能研究作为支撑海洋环境和资源的持续利用的科学基础，已成为海洋科学的前沿领域，必将获得跨越发展。  相似文献   

8.
Characterization of the proteinaceous matter in marine aerosols   总被引：1，自引：0，他引：1  
Marine aerosols play a dominant role in the transfer of oceanic material to the atmosphere. Most marine aerosol originates when air bubbles burst at the sea surface ejecting material from the sea surface microlayer and bubble surface layers into the air. Concentrations of chemical compounds in these surface layers often differ from their concentrations in bulk water. We examined the enrichment of aerosols with proteinaceous matter and attempted to characterize the physical nature and sources of this matter. We measured concentrations of dissolved free (DFAA), dissolved combined (DCAA), and particulate (PAA) amino acids, transparent stainable particles (TSP), and bacteria and virus-like particles as carriers of protein, in natural and simulated aerosols. We also evaluated D/L ratios certain amino acids in all amino acid fractions.DFAA and DCAA enriched the aerosols we sampled by 1.2–20 times compared to bulk seawater; PAA enrichment was usually higher (up to 50-fold). Aerosols contained particles typical of seawater, e.g., microorganisms, organic debris, inorganic particles with adsorbed organic matter, but also a large number of semitransparent gel-like particles, which all contained amino acids. Some of these particles were probably scavenged from bulk water, but new particles produced as bubbles burst at the surface comprised at least 10% of total proteinaceous matter in the aerosol. D/L ratios of certain amino acid suggested that the particles were most likely made from dissolved polymers secreted by phytoplankton that were concentrated on bubble surfaces and in the microlayer. Examination with Alcian Blue (a dye that targets carbohydrates) and Coomassie Blue (a dye that targets proteins) showed that most TSP in the aerosols contained both proteins and polysaccharides. Microorganisms enriched the aerosols by up to two orders of magnitude, but contributed less than 4% to the total protein pool.  相似文献   

9.
Th(IV) isotopes are important proxies in oceanographic investigations, and are used as tracers of particle dynamics and particulate organic matter (POC) fluxes out of the euphotic zone through the use of 234Th/POC ratios. These approaches rely on empirically determined and variable POC to 234Th ratios, which might be controlled, in parts, by the abundance of exopolymeric substances (EPS). EPS contain acidic polysaccharides (APS) and are excreted by both phytoplankton and bacteria. To this end, radiotracer experiments with EPS from microbial cultures were conducted to determine the binding environment of 234Th(IV)-binding ligands in colloids and suspended particles in marine systems. In these experiments, the 234Th distribution during isoelectric focusing (IEF) and polyacrylamide gel electrophoresis (PAGE) was related to the functional group composition of EPS and of colloidal organic matter (COM) isolated from the Gulf of Mexico (GOM) using cross-flow ultrafiltration. EPS was extracted from phytoplankton (Emiliania huxleyi and Synechococcus elongatus) and bacteria (Sagittula stellata and Roseobacter gallaeciensis) cultures by repeated alcohol precipitation. Phosphate and sulfate concentrations were determined using ion chromatography (IC). IEF profiles indicated that 49% to 65% of the 234Th-labeled EPS from plankton and bacteria as well as COM samples from the GOM was found concentrated below pH of 4, near an isoelectric point, pHIEP, of about 2. The carboxylic acid maxima for extracted EPS and COM samples appeared close to the pHIEF of 234Th(IV). The phosphate maximum appeared at the same pHIEF as 234Th(IV) for EPS from R. gallaeciensis and S. elongatus. The sulfate maximum was found at the same pHIEF as 234Th(IV) for EPS from S. elongatus and COM. The molecular weight (MW) of the strongly Th(IV)-binding ligand varied from 1 to 14 kDa, depending on the species, but was about 10 kDa in COM. Thus, depending on the species of plankton or bacteria, the MW and specific functional group composition of the strongly 234Th(IV)-binding amphiphilic biomolecule can vary. Therefore, different acidic functional groups can, at times, contribute to the binding of Th(IV) to the EPS chelating ligand, which can also have different MWs. This implies that the binding environment for Th(IV), which is present at total concentrations at least a million times lower than the acid functional groups, consists of strong polydentate chelate complexes in clustered structures of carboxylate, sulfates and/or phosphates. The combination of strongly chelating groups and amphiphilicity gives this biomolecule the unique properties of a “sticky” ligand.  相似文献   

10.
Cathodic stripping voltammetry (CSV) is used to determine total (after UV-irradiation) and labile dissolved metal concentrations as well as complexing ligand concentrations in samples from the river Scheldt estuary. It was found that even at high added concentrations of catechol (1 m for copper and 0·4 m for iron) and of APDC (1 m for zinc) only part of the dissolved metal was labile (5–58% for copper, 34–69% for zinc, 10–38% for iron); this discrepancy could be explained by the low solubility of iron which is largely present as colloidal material, and by competition for dissolved copper and zinc by organic complexing ligands. Ligand concentrations varied between 28 and 206 n for copper and between 22 and 220 n for zinc; part of the copper complexing ligands could be sub-divided into strong complexing sites with concentrations between 23 and 121 n and weaker sites with concentrations between 44 and 131 n . Values for conditional stability constants varied between (logK′ values) 13·0 and 14·8 for strong and between 11·5 and 12·1 for weaker copper complexing ligands, whereas for zinc the values were between 8·6 and 10·6. The average products of ligand concentrations and conditional stability constants (a-coefficients) were 6 × 102 for zinc and 6 × 106 for copper.The dissolved zinc concentration was found to co-vary with the zinc complexing ligand concentration throughout the estuary. It is argued that the zinc concentration is regulated, in this estuary at least, by interactions with dissolved organic complexing ligands. A similar relationship was apparent between the dissolved copper and the strong copper complexing ligand concentration. The total copper complexing ligand concentrations were much greater than the dissolved copper concentrations, suggesting that only strongly complexed copper is kept in solution.These results provide evidence for the first time that interactions of copper and zinc with dissolved organic complexing ligands determine the geochemical pathway of these metals.  相似文献   

11.
Concurrent distributions of dissolved and suspended particulate organic carbon (DOC and POCsusp), nitrogen (DON and PONsusp) and phosphorus (DOP and POPsusp), and of suspended particulate inorganic phosphorus (PIPsusp), are presented for the open ocean water column. Samples were collected along a three-station transect from the upper continental slope to the abyssal plain in the eastern North Pacific and from a single station in the Southern Ocean. The elemental composition of surface sedimentary organic matter (SOM) was also measured at each location, and sinking particulate organic matter (POMsink) was measured with moored sediment traps over a 110-d period at the abyssal site in the eastern North Pacific only. In addition to elemental compositions, C : N, C : P and N : P ratios were also calculated. Surface and deep ocean concentrations of dissolved organic matter (DOM) and inorganic nutrients between the two sites displayed distinct differences, although suspended POM (POMsusp) concentrations were similar. Concentrations of DOM and POMsusp displayed unique C, N and P distributions, with POMsusp concentrations generally about 1–2 orders of magnitude less than the corresponding DOM concentrations. These differences were likely influenced by different biogeochemical factors: whereas the dissolved constituents may have been influenced more by the physical regime of the study site, suspended particulate matter may have been controlled to a greater extent by biological and chemical alteration. Up to 80% of total particulate P in POMsusp, POMsink and SOM consisted of PIP. For all organic matter pools measured, elemental ratios reveal that organic P is preferentially remineralized over organic C and organic N at both sites. Increases in C : P and N : P ratios with depth were also observed for DOM at both sites, suggesting that DOP is also preferentially degraded over C and N as a function of depth. A simple one-dimensional vertical eddy diffusion model was applied to estimate the contributions of dissolved and suspended particulate organic C, N and P fluxes from the upper mixed layer into the permanent thermocline. Estimated vertical DOM fluxes were 28–63% of the total organic matter fluxes; POMsusp and POMsink fluxes were 8–20 and 28–52% of the total.  相似文献   

12.
Metal-enriched minerals have been widely observed near hydrothermal vent fields.However,the dynamics of particulate metals influenced by hydrothermal activities is poorly constrained.Here,radioactive ~(234)Th in both dissolved and particulate phases were used to examine the kinetics of particle-reactive metal adsorption,removal,and residence in a newly found hydrothermal plume over the Southwest Indian Ridge.The results showed a relatively low value on ~(234)Th/~(238)U ratios(i.e.,0.73-0.88) compared to the deep oceans,indicating an enhanced adsorption of particle-reactive metals onto particulate matter in the plume.Based on the ~(234)Th-~(238)U disequilibria,the adsorption and sinking rate constants of ~(234)Th averaged(0.009±0.001) d~(-1) and(0.113±0.024) d~(-1) in the hydrothermal plume,corresponding to the residence times of(115±19) d and(16±5) d for dissolved and particulate ~(234)Th,respectively.This timescale allows vent-discharged particle-reactive metals to disperse hundreds to thousands of miles away.Thus,hydrothermal activities might influence the metal distribution in deep ocean over a very large scope.Also,a high sinking flux of(36.2±5.4) B q/(m~2·d) for ~(234)Th was observed for the plume,suggesting an enrichment of metal in particles deposited close to the vent.The enhancement of particle sinking could also benefit the transport of organic carbon and nitrogen and fuel the benthic ecosystems under the plume regimes.Thus,hydrothermal plumes may have an impact on both the elemental geochemistry and/or ecosystem to the deep oceans interior than previous expectation.  相似文献   

13.
The Thukela Bank, KwaZulu-Natal, supports a diverse ecosystem and South Africa’s only prawn fishery. Oceanographic studies suggest riverine input is not important for the biology of this system, whereas biological studies suggest the contrary, with prawn catches increasing with increased fluvial run-off. The aim of this study was to determine (i) the importance of riverine and marine organic matter for the Thukela Bank food web; and (ii) whether there are seasonal changes in the Thukela River stable isotope values, and, if so, whether these are reflected in the isotope values of demersal organisms. Estuarine organic matter, sediments and demersal organisms were collected from several sites across the bank in the wet and dry seasons of 2008, 2009 and 2010. Marine particulate organic matter was also collected in 2010 and analysed for δ13C and δ15N, as well as C/N ratios. There were strong seasonal changes in isotopic values of organic matter and fauna, especially faunal δ13C. There was an apparent time-lag in organisms assimilating riverine organic matter isotopic values, with the isotopic signature of demersal organisms reflecting that of riverine organic matter from the previous season, which is likely the result of tissue turnover time. In 2010, Thukela Bank sediment organic matter was of riverine origin and this maintained the demersal food web. We conclude that Thukela River organic matter is an important input to the food web of the Thukela Bank, indicating that any future damming of the catchment area could have serious consequences for this ecosystem.  相似文献   

14.
A method is presented to study the carbohydrate composition of marine objects involved into sedimento- and diagenesis (plankton, particulate matter, benthos, and bottom sediments). The analysis of the carbohydrates is based upon the consecutive separation of their fractions with different solvents (water, alkali, and acid). The ratio of the carbohydrate fractions allows one to evaluate the lability of the carbohydrate complex. It is also usable as an indicator of the biogeochemical processes in the ocean, as well of the genesis and the degree of conversion of organic matter in the bottom sediments and nodules. The similarity in the monosaccharide composition is shown for dissolved organic matter and aqueous and alkaline fractions of seston and particulate matter.  相似文献   

15.
1IntroductionThefluxesofcarbon,nutrients,andassoci-atedelementsinvolvedinthebiogeochemicalcyclesoutoftheeuphoticzoneareimportantinthestudyofglobalCO2 change.Someworkershaveproposedthatatthesteadystatethefluxofparticulateorganiccarbonoutoftheeuphoticzoneequalsthenewproduction(EppleyandPe-terson,1979;Eppley,1989).Generallytwometh-odscanbeemployedtoobtainthefluxdata.Oneistousesedimenttrapsintheupperocean(<200m)orfloatingsedimenttraps.Thoughthesedimenttraptechnologyhasshowntobeuse-fulfortimeser…  相似文献   

16.
The molecular distribution of dissolved proteins in seawater from coastal marine environments in Uranouchi Bay, Kochi Prefecture, is first reported in this article. Occurrence of bacteria-derived dissolved proteins and their source bacteria were examined using a probe of the antibody (anti-Omp35La) against a porin outer membrane protein (Omp35La) of the fish pathogenic bacterium Vibrio (Listonella) anguillarum. The electrophoretograms of dissolved proteins from coastal seawater showed a large number of discrete and individual proteins overlapped each other over a wide range of molecular masses indicating active processes in coastal environments in transferring proteins from organisms to the inanimate dissolved protein pool. Among the dissolved proteins, 37 kDa- and 18 kDa-proteins reacted with the Omp35La. In order to isolate the source bacteria of such dissolved proteins, bacteria from seawater and diseased fish were screened by colony Western blotting with anti-Omp35La. The reactive strains were further examined in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)/Western blotting to verify the presence of Omp35La homologues among the outer membrane proteins of such strains. Outer membrane proteins reacting with anti-Omp35La were detected in only 4 strains of the 129 strains that were positive in the colony Western blotting. The level of possible source bacteria of 37 kDa- and 18 kDa-dissolved proteins was suggested to be 5–6 orders of magnitude lower than the total bacterial count. The present study leads us to hypothesize that a minor portion of the bacterial assemblage is responsible for the dissolved proteins in the coastal waters.  相似文献   

17.
本文阐述了生物海洋学的内容及其研究状况。根据我国沿海特点,建议我国今后对生物海洋学研究的重点是:1.对不同水域初级生产力的研究。2.对沿海小型底栖生物在海洋生态系统能流和物质循环中的作用研究。3.河口,有代表性海域可溶性有机物(DOM)、颗粒有机物(POM)的来源、数量分布、化学组成,以及在海洋食物链的作用和鱼虾产卵场变动关系的研究。4.沿海养殖环境生原要素循环、环境容量及病害发生的环境研究。5.海洋生物对重要有机污染物和海藻毒素的吸收、富集、代谢、在食物链传递,以及生态影响和生态监测研究。6.沿海植物性碎屑向近海输运,及其在食物链中的作用研究。7.浮游生物的群集、支配群集因素,以及和渔业关系的研究。8.选择代表性海域开展物质通量的研究。  相似文献   

18.
Uncertainties in the determinations of particulate organic carbon flux from measurements of the disequilibrium between 234Th and its mother isotope uranium depend largely on the determination of the organic carbon to 234thorium (OC : 234Th) ratio. The variability of the OC : 234Th ratio in different size fractions of suspended matter, ranging from the truly dissolved (< 3 or 10 kDa) fraction to several millimeter sized marine snow, as well as from sediment trap material was assessed during an eight-day cruise off the coast of California in Spring 1997. The affinity of polysaccharide particles called TEP (transparent exopolymer particles) and inorganic clays to 234Th was investigated through correlations. The observed decrease in the OC : 234Th ratio with size, within the truly dissolved to small particle size range, is consistent with concepts of irreversible colloidal aggregation of non-porous nano-aggregates. No consistent trend in the OC : 234Th ratio was observed for particles between 1 or 10 to 6000 μm. Origin and fate of marine particles belonging to this size range are diverse and interactions with 234Th too complex to expect a consistent relationship between OC : 234Th ratio and size, if all categories of particles are included. The relationship between OC and 234Th was significant when data from the truly dissolved fraction were excluded. However, variability was very large, implying that OC flux calculations using different collection methods (e.g. sediment trap, Niskin bottles or pumps) would differ significantly. Therefore a large uncertainty in OC flux calculations based on the 234Th method exist due to individual decisions as to which types or size classes of particles best represent sinking material in a specific area. Preferential binding of 234Th to specific substance classes could explain the high variability in the relationship between OC and 234Th. At 15 m, in the absence of lithogenic material, the OC : 234Th ratio was a function of the fraction of TEP or TEP-precursors in OC, confirming that acidic polysaccharides have a high affinity for 234Th and that TEP carry a ligand for 234Th. Preferential binding to TEP might change distribution patterns of 234Th considerably, as TEP may sink when included in large aggregates, or remain suspended or even ascend when existing as individual particles or microaggregates. In the presence of lithogenic matter, at depths below 30 m, the ratio between 234Th and OC was linearly related to the ratio between alumino silicates and C. The affinity of inorganic substances to 234Th is known to be relatively low, suggesting that a coating of acidic polysaccharides was responsible for the apparently high affinity between 234Th and lithogenic material. Overall, OC : 234Th ratios of all material collected during this investigation can best be explained by differential binding of 234Th to both TEP and TEP-precursors, as well as to lithogenic minerals, which were very abundant in an intermediate nepheloid layer between 50 and 90 m.  相似文献   

19.
234Th is widely used to quantify the magnitude of upper ocean particulate organic carbon(POC)export in oceans.In the present work,the rates of particulate organic carbon export were measured based on the distribution patterns of234Th/238U disequilibrium in the water column within the continental slope of the East China Sea(ECS)during May 2011.The profiles of particulate and dissolved234Th activities at all three stations showed a relative deficit with respect to238U in the upper 100 m of the water column.The dissolved234Th scavenging rates and the particulate234Th removal rates and their residence times were calculated by a one-dimensional steady state model.The results showed that the dissolved234Th scavenging rates and the particulate234Th removal rates ranged from 12.4–61.4 dpm/(m3·d)andfrom3.8–21.8 dpm/(m3·d),respectively.The residence times of dissolved and particulate234Th were in the range of 3.4–158 d and 63.7–96.5 d,respectively.Combined with the measurement of POC/234Th ratios of suspended particles,POC export flux(calculated by carbon)from the euphotic zone was estimated in the study region,which ranged from 4.14–14.7 mmol/(m2·d),withanaverageof8.21mmol/(m2·d),occupying35%oftheprimeproductivity in the study area.The results of this study can provide new information for better understanding the carbon biogeochemical cycle within the continental slope of the ECS.  相似文献   

20.
A new method is proposed for the determination of complexing capacities and conditional stability constants for complexes of copper(II) with dissolved organic ligands in seawater. This method is based on ligand competition by the added ligand catechol for free metal ions. The concentration of copper-catechol complex ions is measured with great sensitivity by cathodic stripping voltammetry. The concentration of the free copper ion is calculated from the concentration of copper-catechol complex ions. Ligand concentrations and conditional stability constants are obtained from a titration of the ligands with copper. Two techniques for treatment of the data are compared. A seawater sample, originating from open oceanic conditions, is analysed and two complexing ligands were detected, having concentrations of 1.1 × 10?8 and 3.3 × 10?8 M, and conditional stability constants (log K′CuL) of 12.2 and 10.2, respectively.  相似文献   

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