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

2.
Polycyclic aromatic hydrocarbons (PAHs) were identified and measured in surface seawater and in the tissues (gills and mantle) of indigenous black mussels, Mytilus galloprovincialis, collected from three coastal sites of Saronikos Gulf (Greece), a gulf that exhibits high levels of pollution. The total PAHs measured by spectrofluorometry in the surface seawater were found in the range of 425–459 ng L−1 at the most polluted sites 1 and 2 (Elefsis Bay–Salamis Island) and in the range of 103–124 ng L−1 at site 3 (Aegina Island). PAHs' sources in seawater were identified by application of specific PAH ratios, such as phenanthrene/anthracene and fluoranthene/pyrene. Levels of PAHs in soft tissues (gills and mantle) of indigenous mussels were much higher than those reported for seawater. Total PAH concentrations in mantle tissues were in the range of 1300–1800 ng g−1 dry weight (dw) tissue at sites 1 and 2 and approximately 380 ng g−1 dw at site 3. In gill tissues total PAH concentrations were in the range of 1480–2400 ng g−1 dw at sites 1 and 2 and approximately 430 ng g−1 dw at site 3. PAHs composition was dominated by two-, three- and four-ring compounds in seawater, where 17 different PAH compounds were identified and measured in mussel tissues. Mussels can be used as sentinel organisms to monitoring PAHs' contamination, since they concentrate PAHs from the surrounding water media and therefore making the chemical analysis simpler and less prone to error than that for water. In surface seawater possible weathering and photodegradation due to hot climates contribute to reduced PAHs concentrations.  相似文献   

3.
Calibration of a chalcogenide glass membrane, Fe(III)ISE [Fe2.5(Ge28Sb12Se60)97.5], in buffered saline media has been undertaken in order to assess the suitability of this ISE for seawater analyses. The electrode slopes in saline citrate and salicylate buffers were 26.3 and 28.2 mV/decade, respectively, for Fe3+ concentrations ranging from 10−10 M to less than 10−25 M Fe3+. The calibration lines in the citrate and salicylate buffers were essentially collinear with the response in unbuffered chloride-free standards containing >10−5 M Fe3+, demonstrating that the response of the FeISE is unaffected by chloride ions. A mechanism involving a combination of charge transfer and ion-exchange of Fe(III), at the electrode diffusion layer, can be used to explain the ≈30 mV/decade slope of the FeISE. The response of the FeISE in UV photooxidised seawater containing 8 nM total Fe was measured as the pH was changed from 8.27 to 3.51. The slope of the response was 24.2 mV/decade [Fe3+] calculated as a function of pH using Fe(III) hydrolysis constants for seawater. Moreover, the response was essentially collinear with that in citrate buffers and in unbuffered solutions containing >10−5 M Fe3+ and the slope for the combined data was 26.2 mV/decade. This study was restricted to organic-free seawater because the certainty in Fe(III)–ligand stability constants is insufficient to warrant the selection of an ideal calibration buffer system, and there is evidence that powerful chelating ligands (e.g., EDTA along with humic and fulvic acids) may alter the response of the Fe(III)ISE. The Fe dissolution rate of the FeISE in UV photooxidised seawater was found to be 1.6×10−2 nmol Fe/min, as measured by cathodic stripping voltammetry (CSV). This would contaminate a 100-ml sample by 0.8–1.6 nM Fe over a typical measurement period of 5–10 min obtained using a stability criterion of 0.5 mV/min. Various methods are proposed for reducing the level of contamination in open ocean samples that contain sub-nanomolar concentrations of iron. The FeISE has the potential to detect free Fe3+ at concentrations typically found in natural seawater.  相似文献   

4.
Shear and Richardson number in a mode-water eddy   总被引：1，自引：0，他引：1  
Measurements of stratification and shear were carried out as part of the EDDIES tracer release experiment in mode-water eddy A4 during the summer of 2005. These measurements were accomplished using both shipboard instrumentation and a drifting mooring. A strong relationship between shear intensity and distance from the center of the eddy A4 was observed with the shipboard ADCP. Diapycnal diffusivity at the SF6 tracer isopycnal prior to and during the release was estimated from the drifting mooring to be 2.9×10−6 m2 s−1. Diffusivity increased by an order of magnitude to 3.2×10−5 m2 s−1 during the period of the final tracer survey in early September, which was similar to the value estimated from the tracer analysis for the whole experiment (3.5×10−5 m2 s−1, [Ledwell, J.R., McGillicuddy Jr., D.J., Anderson, L.A., 2008. Nutrient flux into an intense deep chlorophyll layer in a mode-water eddy. Deep-Sea Research II, this issue [doi:10.1016/j.dsr2.2008.02.005]].  相似文献   

5.
A direct, spectrophotometric method has been adapted for quantitative determination of nitrate concentrations in seawater. The method is based on nitration of resorcinol in acidified seawater, resulting in a color product. The absorption spectrum obtained for the reaction product shows a maximum absorption at 505 nm, with a molar absorptivity of 1.7 × 104 L mol− 1 cm− 1. This method has a detection limit of 0.5 μM and is linear up to 400 μM for nitrate. The advantage of this method is that all reagents are in aqueous solutions without involving cadmium granules as a heterogeneous reactant, as in conventional methods, and therefore is simple to implement. Application of the resorcinol to seawater analysis demonstrated that the results obtained are in good agreement with the conventional approach involving the reduction of nitrate by cadmium followed by diazotization.  相似文献   

6.
Shipboard incubations from the US JGOFS cruise to the Arabian Sea (TN045) March, 1995 showed evidence of iodate reduction in 0.45 μ (Gelman Supor membrane) filtered seawater samples collected from intermediate depths (200–600 m) within the oxygen minimum zone (OMZ). Inorganic chemical reduction of iodate in these samples was ruled out as no free sulfide was measurable and concentrations of ammonia and nitrite were found to be less than 5 μM. To examine whether the reduction of iodate observed at sea could have been the result of bacterial metabolism, reduction of iodate (IO3−) to iodide (I−) by Shewanella putrefaciens strain MR-4 was studied in artificial seawater using electrochemical methods. MR-4 is a ubiquitous marine bacterium which may be of considerable importance when considering redox zonation in the water column because it is a facultative anaerobe and may switch amongst a suite of electron acceptors to support metabolism. In all experiments MR-4 reduced all iodate to iodide. The rate of formation of [I−]in the culture followed pseudo-first order kinetics. This is the first report of the marine bacterial reduction of iodate where the concentrations of iodide and iodate were measured directly. Our results may help to explain the depth distribution of iodine speciation reported in productive waters like the Arabian Sea and for the first time couple iodine speciation with bacterial productivity in the ocean.  相似文献   

7.
Annual production was calculated for the dominant ampeliscid amphipod Ampelisca mississippiana [Soliman, Y., Wicksten, M., 2007. Ampelisca mississippiana a new species (Amphipoda: Gammaredea) dominated the head of the Mississippi Canyon (Northern Gulf of Mexico). Zootaxa, submitted] at the head of the Mississippi Canyon in the northern Gulf of Mexico. Average densities were 12,094±2499 ind m−2, with secondary production of 6.93 g dry wt m−2 yr−1, based on the “size-frequency method” [Hynes-Hamilton, H.B.N., Coleman, M., 1968. A simple method for assessing the annual production of stream benthos. Limnology and Oceanography 13, 569–573; Menzies, C.A., 1980. A note on the Hynes-Hamilton method of estimating secondary production. Limnology and Oceanography 25(4), 770–773], with a production/biomass (P/B) ratio of 3.11. Growth rates of this magnitude are comparable to available data for freshwater and shallow marine ampeliscids, but are unexpectedly high for deep-ocean habitats. Growth efficiency appeared to be approximately 35% (Growth/Assimilation×100).  相似文献   

8.
Lagrangian time series of dimethylsulfide (DMS) concentrations from a cyclonic and an anticyclonic eddy in the Sargasso Sea were used in conjunction with measured DMS loss rates and a model of vertical mixing to estimate gross DMS production in the upper 60 m during summer 2004. Loss terms included biological consumption, photolysis, and ventilation to the atmosphere. The time- and depth (0–60 m)-averaged gross DMS production was estimated to be 0.73±0.09 nM d−1 in the cyclonic eddy and 0.90±0.15 nM d−1 in the anticyclonic eddy, with respective DMS replacement times of 5±1 and 6±1 d. The higher estimated rate of gross production and lower measured loss rate constants in the anticyclonic eddy were equally responsible for this eddy's 50% higher DMS inventory (0–60 m). When normalized to chlorophyll and total dimethylsulfoniopropionate (DMSP), estimated gross production in the anticyclonic eddy was about twice that in the cyclonic eddy, consistent with the greater fraction of phytoplankton that were DMSP producers in the anticyclonic eddy. Higher rates of gross production were estimated below the mixed layer, contributing to the subsurface DMS maximum found in both eddies. In both eddies, gas exchange, microbial consumption, and photolysis were roughly equal DMS loss terms in the surface mixed layer (0.2–0.4 nM d−1). Vertical mixing was a substantial source of DMS to the surface mixed layer in both eddies (0.2–0.3 nM d−1) owing to the relatively high DMS concentrations below the mixed layer. Estimated net biological DMS production rates (gross production minus microbial consumption) in the mixed layer were substantially lower (by almost a factor of 3) than those estimated in a previous study of the Sargasso Sea, which may explain the relatively low mixed-layer DMS concentrations found here during July 2004 (3 nM) compared to previous summers (4–6 nM).  相似文献   

9.
Beginning June of 1993 suites of 13 water samples have been collected at Oyster Landing, North Inlet (SC), every 20 days covering two consecutive tidal cycles at 2.07 h intervals. In order to ascertain whether this large (and still growing) water chemistry data set can be used to determine tidal fluxes of nutrients and sediments, we coupled measured concentrations to estimates of instantaneous tidal discharge based on a basin water storage curve and hindcast tides. The mean advective fluxes of all constituents, including salt, showed statistically significant exports. This result, however, is largely due to an ebb bias in the sampling protocol, which resulted in 52% of the samples being collected on ebb tide versus a theoretical percentage of 48%. When this bias was corrected by reducing the mean discharge (−610 l s−1) to a value (−125 l s−1) that produced a balance between the mean advective and dispersive salt fluxes, the advective fluxes of the other constituents were reduced to values that are not significantly different from zero. In addition to a statistically significant dispersive influx of salt, significant dispersive exports were found for DON, NH4, DOP, PO4 and DOC. All particulate constituents (PN, PP, ISS and OSS) yielded dispersive fluxes that were not significantly different from zero. Annual material budgets for the Oyster Landing basin based on the dispersive fluxes of all constituents (except salt) are generally similar in magnitude and direction to those measured by [Dame, R.F., Spurrier, J.D., Williams, T.M., Kjerfve, B., Zingmark, R.G., Wolaver, T.G., Chrzanowski, T.H., McKeller, H.N., Vernberg, F.J., 1991. Annual material processing by a salt marsh-estuarine basin in South Carolina, USA. Marine Ecology Progress Series 72, 153–166.] in the nearby and ecologically similar Bly Creek basin, indicating that the dispersive fluxes determined in this study are realistic. We offer suggestions for improving the reliability and usefulness of future Oyster Landing water quality data.  相似文献   

10.
Continental margins exert a strong influence on global biogeochemical cycles; however there have been relatively few attempts to quantify either the magnitude or nature of temporal variability in material fluxes. At present here are no reports on nutrient fluxes at the mouth of the Gulf of California (GC) so further information is needed to provide estimated values from direct measurements. From 1995–1999 during five cruises covering all seasons, seawater samples were collected and measured the nutrient content from the surface to the bottom (some deeper than 2500 m) from a repeated hydrographic sections at the mouth of the GC. This chemical and physical database is unique because it covers an area with important biogeochemical signs, which has been detected as one of the highest in primary productivity of the world oceans. These sections are perpendicular to the coastlines of the Mexican states of Baja California Sur (BCS) and Sinaloa. In this section, the most dynamic area was the surface waters in February 1999 with strong geostrophic currents and temperatures of 20 ± 1.5 °C; salinity 35.091 ± 0.156; pH 8.16 ± 0.13; phosphate 0.85 ± 0.42 μM, nitrate + nitrite 2.35 ± 2.94 μM, and ammonia 2.00 ± 1.25 μM (average ± standard deviation).Geostrophic velocities were computed from high-resolution CTD sections across the entrance to the GC. During winter and spring, the outflow occurred near BCS and the inflow occurred either through the center of the section and/or along the Sinaloa coast. Both inflow and outflow cores were 45 km wide and extended deeper than 700 m. Summer and fall showed a complex pattern, alternating cores of inflow and outflow but with inflow along Sinaloa on all cruises. The maximum flow into the Gulf occurs during May in the center of the section while outflow was concentrated along BCS. Mascarenhas et al. [Mascarenhas, A., Castro, R., Collins, C.A., Durazo, R., 2004. Seasonal variation of geostrophic velocity and heat flux at the entrance to the Gulf of California, Mexico. Journal Geophysical Research, 2124.] calculated the section mean geostrophic velocity that was composed of two alternating cores of inflow and outflow. The two cores that were adjacent to either coast were broader and contained the highest inflow (0.40 m s− 1) and outflow (− 0.25 m s− 1) velocities, supporting the general idea of inflow along the Sinaloa and an outflow along BCS.The highest nutrient fluxes occur during El Niño conditions in November 1997 with outflows as high as 54.5 Tg yr− 1 for Phosphate, 43.0 Tg yr− 1 for Nitrate and 31.7 Tg yr− 1 for Ammonia, this values were at least three times higher than in February 1999.  相似文献   

11.
The kinetics of aggregation of riverine colloidal iron have been examined using a stopped-flow technique which probes the first few seconds of mixing between river and sea water end members. A significant fraction, up to 80%, of the colloidal iron is aggregated during the first 1–2 s of mixing, indicating that the aggregation process is much faster than previously thought. Most of the aggregation induced by seawater results from the divalent cations Mg2+ and Ca2+, with the overall ionic strength having little influence. At equal concentrations of 27 mM, the rate of aggregation by alkaline earth cations increased with ionic size Mg2+ < Ca2+ < Sr2+ < Ba2+. The aggregation rates were indifferent to the anion (Cl− or SO42−) present. Very high aggregation rates were also induced by the common water treatment coagulant Al2(SO4)3 at concentrations in the range 20–30 µM Al(III), several orders of magnitude lower that those used for the seawater cations. Our results support the view that specific chemical interactions between the cations and the colloid particle surface, rather than simple electrical effects, control the colloid stability.  相似文献   

12.
Samples of lake water and coastal seawater from Nova Scotia, Canada, were irradiated with natural or artificial sunlight to investigate the potential for photochemical hydrogen production. Hydrogen photo-production was observed in all natural water samples. Rates of hydrogen formation were highest in coloured lake water (range: 98–163 pmol L− 1h− 1) and lower in seawater (range: 19–45 pmol L− 1 h − 1). Dilutions of the most highly coloured lake sample (Kejimkujik Lake) showed a positive linear relationship between H2 production rates and CDOM concentration. Photo-production rates normalised to UV absorption coefficients at 350 nm indicated that the photochemical efficiency of hydrogen formation varied between samples, perhaps due to differences in the CDOM composition. Photochemical hydrogen formation was also seen in solutions of syringic acid and acetaldehyde: two low-molecular-weight carbonyl compounds found in natural waters. Photochemistry may therefore offer least a partial explanation for the persistently high levels of hydrogen observed in the low-latitude surface ocean.  相似文献   

13.
Dissolved gaseous mercury (DGM) was measured continuously using two newly developed techniques and a manual technique. The continuous techniques were based on the equilibrium between the aqueous and gaseous phase (DGM = Hgextr / H', Hgextr is the measured mercury concentration in the gas phase, H' is the Henry's Law coefficient at the desired temperature). In order to calculate the annual mercury evasion from the Mediterranean Sea, diurnal and seasonal measurements of DGM, total gaseous mercury in air (TGM), water temperature and wind speed were performed. During August 2003, March–April 2004 and October–November 2004 measurements of these parameters were conducted on board the RV Urania. The continuous measurements of DGM showed a diurnal variation in concentration, at both coastal and off shore sites, with higher concentrations during daytime than nighttime. The concentration difference could be as large as 130 fM between day and night. The degree of saturation was calculated directly from the measurements, S = Hgextr / TGM and was found to vary between the different seasons. The highest average degree of saturation (850%) and the largest variation in saturation (600–1150%) was observed during the summer. The spring showed the lowest variation (260–360%) and the lowest average degree of saturation (320%). The autumn also showed a large variation in saturation (500–1070%) but a lower average (740%) compared to the summer cruise. This might be explained by the temperature difference between the different seasons, since that parameter varied the most. The flux from the sea surface was calculated using the gas exchange model developed by Nightingale et al. [Nightingale, P.D., Malin, G., Law, C.S., Watson, A.J., Liss, P.S., Liddicoat, M.I., Boutin, J., Upstill-Goddard, R. C., 2000. In situ evaluation of air–sea gas exchange parameterization using novel conservative and volatile tracers. Global Biogeochemical Cycles, 14(1):373–387]. The evasion varied between the different seasons with the highest evasion during the autumn, 24.6 pmol m− 2 h− 1. The summer value was estimated to 22.3 pmol m− 2 h− 1 and the spring to 7.6 pmol m− 2 h− 1. Using this data the yearly evasion from the Mediterranean Sea surface was estimated to 77 tons.  相似文献   

14.
Wet atmospheric deposition of dissolved N, P and Si species is studied in well-mixed coastal ecosystem to evaluate its potential to stimulate photosynthetic activities in nutrient-depleted conditions. Our results show that, during spring, seawater is greatly depleted in major nutrients: Dissolved Inorganic Nitrogen (DIN), Dissolved Inorganic Phosphorus (DIP) and Silicic acid (Si), in parallel with an increase of phytoplanktonic biomass. In spring (March–May) and summer (June–September), wet atmospheric deposition is the predominant source (>60%, relative to riverine contribution) for nitrates and ammonium inputs to this N-limited coastal ecosystem. During winter (October–February), riverine inputs of DIN predominate (>80%) and are annually the most important source of DIP (>90%). This situation allows us to calculate the possibility for a significant contribution to primary production in May 2003, from atmospheric deposition (total input for DIN ≈300 kg km−2 month−1). Based on usual Redfield ratios and assuming that all of the atmospheric-derived N (AD-N) in rainwater is bioavailable for phytoplankton growth, we can estimate new production due to AD-N of 950 mg C m−2 month−1, during this period of depletion in the water column. During the same episode (May 2003), photosynthetic activity rate, considered as gross primary production, was estimated to approximately 30 300 mg C m−2 month−1. Calculation indicates that new photosynthetic activity due to wet atmospheric inputs of nitrogen could be up to 3%.  相似文献   

15.
The effect of ionic interactions on the kinetics of disproportionation of HO2, and the oxidation of Fe(II) and Cu(I) has been examined. The interactions of O2 with Mg2+ and Ca2+ ions in seawater increases the lifetime by 3–5 times compared to water. The effect of OH− on the oxidation of Fe(II) in water and seawater shows a second degree dependence from 5 to 45°C. The effect of salinity on the oxidation of Fe(II) was found to be independent of temperature, while the effect of temperature was found to be independent of salinity. The energy of activation for the overall rate constant was found to be 7 ± 0.5 kcal mol−1.The effect of pH, temperature, salinity and ionic composition on the oxidation of Cu(I) has also been examined. In NaCl solutions from 0.5 to 6 M, the log k for the oxidation was a linear function of pH (6–8) with a slope of 0.2 ± 0.05. The reaction was strongly dependent on the Cl− concentration with variation of from 0.3 to 340 min from 0.5 to 6 M Cl−. The rates of oxidation of Cu+ and CuCl0 responsible for these effects are dependent upon ionic strength. The energy of activation for the reaction was 8.5–9.9 kcal mol−1 from 0.5 to 6 M. Studies of the oxidation in various NaX salts (X = I−, Br− and Cl−) give rates in the order Cl− > Br− > I− as expected, due to complex formation of Cu+ with X−.  相似文献   

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

17.
Data for uranium concentrations in 29 rivers and eight estuaries are presented. The river data expands the existing database on riverine uranium transport to include more smaller watersheds which collectively account for a large portion of material transport from the continent to the oceans. Riverine concentrations for these smaller watershed range from less than 50 to 660 pM. The results for these systems, when combined with previously published data on mostly larger rivers, do not change significantly the calculated global riverine flux and thus earlier estimates by Palmer and Edmond [Palmer, M.R., Edmond, J.M., 1993. Uranium in river water. Geochim. Cosmochim. Acta, 57, pp. 4947–4955] are substantiated. Uranium transport through eight diverse estuaries was studied to assess the importance of estuarine removal in the global marine uranium budget. Results indicate that uranium is conservatively transported in most systems studied. Results reported here for the Savannah estuary, however, indicate significant uranium removal. Our results suggest that uranium is removed in salt marsh estuaries at a rate of ca. 70 μmol/m2. This compares to a rate of 15 μmol/m2 for Delaware salt marshes [Church, T.M., Sarin, M.M., Fleisher, M.Q., Ferchlman, T.G., 1996. Salt marshes: an important sink for dissolved uranium. Geochim. Cosmochim. Acta, 60, pp. 3879–3887]. We suggest that uranium removal to salt marsh sediments is due to anaerobic microbially mediated processes. We use these results to estimate the global significance of the salt marsh sink in the oceanic budget of uranium. We estimate that 2.7×107 mol of uranium are removed to salt marshes annually as compared to an annual global riverine input of 3–6×107 mol estimated by Palmer and Edmond [Palmer, M.R., Edmond, J.M., 1993. Uranium in river water. Geochim. Cosmochim. Acta, 57, pp. 4947–4955].  相似文献   

18.
Vertical and seasonal characteristics of biogenic silica (BSi) dissolution in seawater were investigated by multiple dissolution experiments using seawater collected from surface and mesopelagic layers in Suruga Bay during the period 2002–2004. The dissolution rate coefficients calculated based on temporal changes of BSi concentration varied with the season of sample collection. They ranged from 0.023–0.057 day− 1 for surface samples and 0.0018–0.0025 day− 1 for mesopelagic samples for temperatures approaching in situ conditions. Experiments at various temperatures confirmed that BSi dissolution depends on temperature in natural seawater. Dissolution rate coefficient (day− 1) of BSi correlated significantly with temperature (°C), and Q10 was 2.6. Addition of bioavailable organic matter to low-bioactivity seawater enhanced the protease activity and abundance of bacteria, and increased BSi dissolution rate by a factor of 1.4–2.0. There is clear evidence that BSi dissolution is accelerated by bacterial activity and potentially limited by bioavailable organic matter in natural seawater. Dissolution rates and total decreases of BSi concentration were lower during experiments using mesopelagic samples than in those using surface samples. This suggests that dissolution of BSi varies with depth and that BSi in the mesopelagic water is more resistant to the dissolution than that in the surface water. This lower dissolution rate was caused by lower temperature and lower bacterial activity due to less bioavailable organic matter in mesopelagic water. Our results provide a mechanistic understanding of variations in silica cycling within the seasonally and vertically differing marine environment.  相似文献   

19.
Field investigations on the population dynamics of Nereis diversicolor were carried out from January 2002 to December 2003 in the estuary of Oued Souss (southwestern Morocco) to determine the changes caused by setting up of a domestic and industrial wastewater purification plant (M'zar) before and after by the end of wastewater discharges in November 2002 on the structure of the ecosystem. Samples of N. diversicolor were collected monthly in the intertidal zone at low tide before (during 2002) and after (during 2003) the end of wastewater discharges.Separation of cohorts using the Algorithm EM method (McLachlan, G.J., Krishnan, T., 1997. The EM algorithm and extensions. Wiley Series in Probability and Statistics. Wiley, New York, 274 pp.) allowed determination of the growth rate (mm day−1) by cohort and the annual production. The data showed significant differences between populations of Nereis diversicolor before and after the end of wastewater discharges. During the wastewater discharge period (2002), the population had a mean annual density of 1992 ind m−2, a mean annual biomass of 75.52 g DW m−2 and an annual secondary production of 141.3 g DW m−2 with a P/B ratio of 1.87. After the end of discharges (2003), density, biomass and secondary production decreased significantly. The annual averages for these parameters were 740 ind m−2, 14.16 g DW m−2 and 23.83 g DW m−2, respectively, with a P/B ratio of 1.68.The important decrease observed in density, biomass and secondary production of Nereis diversicolor may be attributed (a) to the environmental changes observed after the end of wastewater discharges in the estuary of Oued Souss, namely the increase of salinity and the decrease of organic matter content, and (b) to the migration of this species towards other areas.  相似文献   

20.
Methylmercury (MeHg) concentration and production rates were studied in bottom sediments along the mainstem of Chesapeake Bay and on the adjoining continental shelf and slope. Our objectives were to 1) observe spatial and temporal changes in total mercury (HgT) and MeHg concentrations in the mid-Atlantic coastal region, 2) investigate biogeochemical factors that affect MeHg production, and 3) examine the potential of these sediments as sources of MeHg to coastal and open waters. Estuarine, shelf and slope sediments contained on average 0.5 to 1.5% Hg as MeHg (% MeHg), which increased significantly with salinity across our study site, with weak seasonal trends. Methylation rate constants (kmeth), estimated using enriched stable mercury isotope spikes to intact cores, showed a similar, but weaker, salinity trend, but strong seasonality, and was highly correlated with % MeHg. Together, these patterns suggest that some fraction of MeHg is preserved thru seasons, as found by others [Orihel, D.M., Paterson, M.J., Blanchfield, P.J., Bodaly, R.A., Gilmour, C.C., Hintelmann, H., 2008. Temporal changes in the distribution, methylation, and bioaccumulation of newly deposited mercury in an aquatic ecosystem. Environmental Pollution 154, 77] Similar to other ecosystems, methylation was most favored in sediment depth horizons where sulfate was available, but sulfide concentrations were low (between 0.1 and 10 μM). MeHg production was maximal at the sediment surface in the organic sediments of the upper and mid Bay where oxygen penetration was small, but was found at increasingly deeper depths, and across a wider vertical range, as salinity increased, where oxygen penetration was deeper. Vertical trends in MeHg production mirrored the deeper, vertically expanded redox boundary layers in these offshore sediments. The organic content of the sediments had a strong impact on the sediment:water partitioning of Hg, and therefore, on methylation rates. However, the HgT distribution coefficient (KD) normalized to organic matter varied by more than an order of magnitude across the study area, suggesting an important role of organic matter quality in Hg sequestration. We hypothesize that the lower sulfur content organic matter of shelf and slope sediments has a lower binding capacity for Hg resulting in higher MeHg production, relative to sediments in the estuary. Substantially higher MeHg concentrations in pore water relative to the water column indicate all sites are sources of MeHg to the water column throughout the seasons studied. Calculated diffusional fluxes for MeHg averaged  1 pmol m− 2 day− 1. It is likely that the total MeHg flux in sediments of the lower Bay and continental margin are significantly higher than their estimated diffusive fluxes due to enhanced MeHg mobilization by biological and/or physical processes. Our flux estimates across the full salinity gradient of Chesapeake Bay and its adjacent slope and shelf strongly suggest that the flux from coastal sediments is of the same order as other sources and contributes substantially to the coastal MeHg budget.  相似文献   

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