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1.
The speciation of dissolved iodine and the distributions of the iodine species in the deep Chesapeake Bay underwent seasonal variations in response to changes in the prevailing redox condition. In the deep water, the ratios of iodate to iodide and iodate to inorganic iodine decreased progressively from the Winter through the Summer as the deep water became more poorly oxygenated before they rebounded in the Fall when the deep water became re-oxygenated again. The composition of the surface water followed the same trend. However, in this case, the higher biological activities in the Spring and the Summer could also have enhanced the biologically mediated reduction of iodate to iodide by phytoplankton and contributed to the lower ratios found during those seasons. Superimposed on this redox cycle was a cycle of input and removal of dissolved iodine probably as a result of the interactions between the water column and the underlying sediments. Iodine was added to the Bay during the Summer when the deep water was more reducing and removed from the Bay in the Fall when the deep water became re-oxygenated. A third cycle was the inter-conversion between inorganic iodine and ‘dissolved organic iodine’, or ‘‘DOI’’. The conversion of inorganic iodine to ‘DOI’ was more prevalent in the Spring. As a result of these biogeochemical reactions in the Bay, during exchanges between the Bay and the North Atlantic, iodate-rich and ‘DOI’-poor water was imported into the Bay while iodide- and ‘DOI’-rich water was exported to the Atlantic. The export of iodide from these geochemically reactive systems along the land margins contributes to the enrichment of iodide in the surface open oceans.  相似文献   

2.
The distributions of iodide, iodate and total iodine were determined along a transect from the Sargasso Sea and across the Gulf Stream to the continental shelf of the South Atlantic Bight during November 1990. The western boundary of the Gulf Stream at the outer shelf-upper slope was characterized by steeply sloping isotherms and isopleths of iodide and iodate, resulting from a dome of cold water that was rich in iodate and nearly devoid of iodide at the slope. Both the mid and the inner shelf were relatively well mixed vertically. The concentration of iodate in the surface waters decreased shoreward from >0.3 μM in the Sargasso Sea/Gulf Stream/outer shelf, to 0.29 μM in the midshelf, 0.19 μM in the outer-inner shelf and 0.11 /IM in the inner-inner shelf. Concomitantly, the concentration of iodide increased from <161 nM to 175 nM, 257 nM and 300 nM. The concentration changes were more abrupt in the inner-inner shelf within about 30 km from the shore. There was no evidence of significant concentrations of organic iodine. These distributions of iodide and iodate suggest that the South Atlantic Bight may act as a geochemical processor of dissolved iodine. Iodate is added to the shelf during topographically induced upwelling and frontal exchange with the Gulf Stream. In the shelf waters, iodate is reduced to iodide in situ. Iodide is exported from the shelf to the Gulf Stream which may eventually further transport it to the ocean interior. A ☐ model calculation suggests that 28% and 43% of the iodate added to the Bight and the inner shelf, respectively, are converted to another form in these waters, almost all of which is iodide. About a third of the reduction of iodate to iodide in the Bight occurs in the inner shelf. Thus, the inner shelf may be the most geochemically active zone within the Bight. The residence times of iodide relative to its production and that of iodate relative to its removal are 3.1 and 3.6 months in the Bight and 0.9 and 1.8 months in the inner shelf.  相似文献   

3.
Dissolved iodate and total iodine were studied in St Helena Bay, South Africa, during a period of acute hypoxia, following upwelling off Cape Columbine. Despite the generally high concentrations of chlorophyll α (10–30 mg m−3) total iodine concentration was essentially constant in the main part of the Bay, and similar to that found elsewhere in the oceans. Occasional, lower concentrations of total iodine (0·28 to 0·42 μM) were found with exceptionally high chlorophyll α concentrations (500 mg m−3) in shallow waters. In contrast, iodate was found to be reduced to iodide at both the surface and the bottom of the Bay. The implications of these changes are discussed, given that the surface waters reflect sustained eutrophication while the bottom waters are hypoxic as a result of the organic-rich sediment from the waters above.  相似文献   

4.
The temporal variation of iodate and total iodine in the Menai Straits and Irish Sea is discussed together with station data for the Atlantic Ocean. Surprisingly little temporal variation was found in either iodate or total iodine even though seasonal nutrient cycling occurred within these water bodies. The iodate concentrations of the temperate Atlantic Ocean, Irish Sea and Menai Straits surface waters were significantly different. These results, together with the known hydrology of the Menai Straits, make it likely that iodate-reducing substances present in terrestrial run-off will be responsible for relatively low iodate concentrations in shallow-seawaters, such as the Irish Sea. However, it is suggested that the low iodate concentrations of tropical surface waters are more likely to have a biological origin. The possibility that the marine iodine system is open to a thermo-dynamical interpretation, as some workers have suggested, is refuted in the case of temperate surface waters as well as deep ocean waters (>200 m). It is shown that existing analyses indicate that below 200 m at oceanic stations, iodate does not vary significantly with depth.  相似文献   

5.
Victor W. Truesdale   《Marine Chemistry》2007,104(3-4):266-281
Aerated solutions of potassium iodide in de-ionised water, of between 5–20% (w/v), were exposed to ambient spring sunlight to estimate the rate of photochemical production of molecular iodine from iodide and oxygen in seawater. This rate cannot be measured directly as other reactions, for example the reduction of molecular iodine by organic matter, interfere. Also, a parallel photo-oxidation, initiated by organic matter in real seawater, may also occur. The experiments yield a half-life for iodide in tropical surface waters of about 29 months suggesting that the reaction is insignificant. At this rate it will not compete effectively against the reduction of molecular iodine by organic matter, and hence molecular iodine should not appear. The experiments also consider the photo-oxidation by nitrate, and iodate, a combination of nitrite and oxygen, and eliminate significant interference by chloride, bromide and the phosphate buffer. The rate of photo-oxidation with each of the first three oxidations is found to be first order with respect to oxidant concentration. The variation of photo-oxidation rate with pH is also studied, with a brief investigation without conventional oxidant, where electron cage complexes still promote photo-oxidation. The photochemical action spectrum for these reactions in sunlight is shown to extend between 300 and 425 nm. The photo-oxidation of iodide by iodate is more interesting to marine chemistry as the photo-reduction of iodate. Nevertheless, the reduction-rate is judged to be several orders too low to be significant in seawater. The mechanism of the reactions are discussed and lessons drawn on the stability of potassium iodide solutions used in iodate analysis. The KI actinometer is recommended to those studying other photochemical systems activated by UV-A light as it is linear and very simple and reliable.  相似文献   

6.
This study was performed in order to obtain information on the influence of an acute anoxic event (September, 1997) on distribution and speciation of inorganic iodine in the water column of a small, intensely eutrophicated salt lake. The variations in iodate and iodide depth distributions during the investigated period (1998–2000) were in accord with seasonal changes in redox conditions. During the stratification period (spring and summer), the concentration ratio between iodate and iodide in the upper layers was high, whereas during late summer and autumn, as a result of water column de-stratification and mixing of highly reducing deep water with the oxic layer, lower ratios and more uniform depth distributions were observed.The massive mortality of lake organisms induced by anoxic conditions and sulphide presence throughout the water column was registered by the end of September 1997, when overturn of the lake occurred. The concentrations of iodate in the oxic upper layers were elevated for more than a year after the mass-mortality event (up to 0.55 μmol L−1), whereas iodide concentrations remained high for more than 2 years in deep anoxic water (up to 2.27 μmol L−1). These data suggest that biogeochemical renewal processes affecting the concentrations of inorganic iodine in the lake water are slow compared to those that govern the speciation of iodine. The role of sediment–water interactions and iodine-rich organic species in the production of iodide are discussed.  相似文献   

7.
Iodide and iodate concentrations are reported and discussed for the WOCE A23 transect from the Weddell Sea north to about 25°S. Iodide concentrations are very low in the surface waters of the Weddell Sea (20 nM) and increase steadily northwards to about 100 nM in the surface waters of the south Atlantic gyre. In deep waters iodide concentrations are low but detectable at 0.5–2 nM. There is no detectable total iodine depletion in the surface waters south of the polar front although there is a small depletion evident north of the front. The results are discussed in terms of the hydrography, nutrient concentrations and phytoplankton activity along the transect. In particular, a systematic change in the relationship between iodide and nitrate along the transect is discussed.  相似文献   

8.
A study of inorganic iodine speciation in the waters of seven Croatian coastal caves is described. These are anchialine caves as they are connected hydraulically with Adriatic Sea surface water, with the tide inside the cave rising and falling with that outside, but replenishment of the water is restricted by the karst rock. In effect, the water in the cave probably acts more like a piston, and although moving slightly vertically, has a long residence time compared to a fully-flushing cave. Anchialine environments display a number of unusual features, e.g., a well-developed pycnocline, hypoxia and endemic fauna. Iodate and iodide were determined by differential pulse voltammetry and cathodic stripping square wave voltammetry, respectively. Low iodide concentrations (< 10 nM) have been consistently identified in the bottom water of the caves where concentrations of 90–100 nM would ordinarily be expected from intrusion of Eastern Adriatic surface seawater. Where total inorganic iodine concentrations behave conservatively with salinity the loss of the iodide implies oxidation to iodate. As iodide oxidation remains one of the enduring academic problems of the marine iodine system the study of iodine in anchialine caves may help unravel it. Iodate reduction was observed in mid-water, at the halocline, and mechanisms for the reduction involving either respiration or chemolitho-autotrophic bacteria are considered. The respiration mechanism is favoured because of enhanced alkalinity found in the near surface waters of the caves.  相似文献   

9.
A combination of CTD casts, discrete bottle sampling and in situ voltammetric microelectrode profiling was used to examine changing redox conditions in the water column at a single station south of the Bay Bridge in the upper Chesapeake Bay in late July/early August, 2002–2005. Short-term (2–4 h) fluctuations in the oxic/suboxic/anoxic interface were documented using in situ voltammetric solid-state electrodes. Profiles of dissolved oxygen and sulfide revealed tidally-driven vertical fluctuations of several meters in the depth and thickness of the suboxic zone. Bottom water concentrations of sulfide, Mn2+ and Fe2+ also varied over the tidal cycle by approximately an order of magnitude. These data indicate that redox species concentrations at this site varied more due to physical processes than biogeochemical processes. Based on analysis of ADCP data, tidal currents at this station were strongly polarized, with the principal axis of tidal currents aligned with the mainstem channel. Together with the chemical data, the ADCP analysis suggests tidal flushing of anoxic bottom waters with suboxic water from north of the site. The present study is thus unique because while most previous studies have focused on processes across relatively stable redox interfaces, our data clearly demonstrate the influence of rapidly changing physical mixing processes on water column redox chemistry.Also noted during the study were interannual differences in maximum bottom water concentrations of sulfide, Mn2+ and Fe2+. In 2003, for example, heavy spring rains resulted in severe hypoxia/anoxia in June and early July. While reported storm-induced mixing in late July/early August 2003 partially alleviated the low-oxygen conditions, bottom water concentrations of sulfide, Mn2+ and Fe2+ were still much higher than in the previous year. The latter implies that the response time of the microbial community inhabiting the suboxic/anoxic bottom waters to changing redox conditions is slow compared to the time scale of episodic mixing events. Bottom water concentrations of the redox-sensitive chemical species should thus be useful as a tracer to infer prior hypoxic/anoxic conditions not apparent from ambient oxygen levels at the time of sampling.  相似文献   

10.
Dissolved iodine in waters overlying and in the Orca Basin,Gulf of Mexico   总被引：1，自引：0，他引：1  
The distribution and speciation of iodine, a biophilic redox-sensitive trace element, in waters overlying and in the Orca Basin, Gulf of Mexico, which contains hypersaline, anoxic and yet non-sulfide-bearing brine have been determined. The distribution of iodate and iodide in the oxic waters overlying the anoxic brine are similar to those reported in other oceans. However, in the oxic-anoxic mixing zone, iodate disappears while the concentration of iodide reaches a maximum of 8.1 μM, the highest concentration ever reported in open oceans. There is also a maximum in specific iodine of 30.7 nM‰?1 at this depth. Specific iodine in oxic seawater is only about 10–14 nM ‰?1. These features may be explained by the preferential dissolution of biogenic particles that have accumulated in a strong pycnocline. In the anoxic brine proper, the concentration of iodide is 3.8 μM and can be explained almost entirely by the simultaneous mobilization of chloride and iodide during the dissolution of evaporite beds as the specific iodine of 14.5 nM‰?1 is only slightly higher than those observed in the oxic waters.  相似文献   

11.
Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10−4 mol I m−2 a−1. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO3−/I− and I2/I− couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.  相似文献   

12.
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   

13.
Dissolved titanium distributions in the Mid-Atlantic Bight   总被引：1，自引：0，他引：1  
Stephen A. Skrabal   《Marine Chemistry》2006,102(3-4):218-229
Although titanium is abundant in Earth's crust, its sources and distribution in the ocean are poorly understood. To elucidate its behavior, distributions of dissolved (< 0.2 μm) Ti were determined in surface waters and vertical profiles from the Mid-Atlantic Bight (MAB). Concentrations of Ti decreased from 390 pM at the Delaware Bay mouth to < 100 pM across the Delaware continental shelf. In vertical profiles, small increases in bottom waters suggest a possible flux of Ti from shelf sediments, consistent with previous reports of pore water enrichments of dissolved Ti in MAB sediments. Concentrations in surface waters of the outer shelf and slope ranged between 30 and 140 pM, with most values below 90 pM. Concentrations in a 1000 m vertical profile in the eastern Gulf Stream ranged between 110 and 280 pM, and showed a variable distribution attributed to the mixing of water masses in the outer MAB. A simple model of Ti sources to the MAB suggests that atmospheric deposition of dissolved Ti is comparable to net riverine contributions and therefore must be considered in applications of Ti as a tracer of oceanographic processes.  相似文献   

14.
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   

15.
Toward assessing the biogeochemical significance of seaweeds in relation to dissolved iodine in seawater, the effect of whole seaweeds (Laminaria digitata and Fucus serratus) upon iodide and iodate, at essentially natural concentrations, has been studied. The weeds were carefully removed from the sub-littoral zone of the Menai Straits and exposed to iodide and iodate at their natural temperature (6 °C), but under continuous illumination. Laminaria digitata was found to decrease the concentration of iodate with an exponential rate constant of 0.008–0.24 h−1. This is a newly discovered process which, if substantiated, will require an entirely new mechanism. Generally, apparent iodide concentration increased except in a run with seawater augmented with iodide, where it first decreased. The rate constant for loss of iodide was 0.014–0.16 h−1. Meanwhile, F. serratus was found not to decrease iodate concentrations, as did L. digitata. Indeed, after ∼30 h iodate concentrations increased, suggesting that the weed may take in iodide before oxidising and releasing it. If substantiated, this finding may offer a way into one of the most elusive of processes within the iodine cycle – iodide oxidation. With both seaweeds sustained long-term increases of apparent iodide concentration are most easily explained as a secretion by the weeds of organic matter which is capable of reducing the Ce(IV) reagent used in determination of total iodine. Modelling of the catalytic method used is provided to support this contention. The possibility of developing this to measure the strain that seaweeds endure in this kind of biogeochemical flux experiment is discussed. A Chemical Oxygen Demand type of approach is applied using Ce(IV) as oxidant. The results of the iodine experiments are contrasted with the several investigations of 131I interaction with seaweeds, which have routinely used discs of weed cut from the frond. It is argued that experiments conducted with stable iodine may measure a different variable to that measured in radio-iodine experiments.  相似文献   

16.
Dissolved iodine species and the relationship between its distribution and salinity in Jiulong River estuarine water have been determined. It has been found that the total iodine, iodate and iodide are positive linear with salinity. This indicates that dissolved iodine species (IO-3 and I- ) in estuarine water .how conservative behaviour. The river water contains 2. 40μg/1 as iodide and less than 1. 0μg/1 as iodate, and iodide is the predominant species. Whereas the sea water contains 39. 4μg/1 as iodate and 4. 00μg/1 as iodide, and iodate is the dominant form. The distribution of dissolved iodine in pore water, as a function of depth, has been studied. Iodine in pore water occurs as iodide. The apparent fluxes of soluble iodine from the sediment to the overlying water in the estuary have been determined. The values are 2. 4 (15℃) and 27μmol/(m2·d) (30℃) respectively.  相似文献   

17.
The development of procedures for the determination of iodate- and total-iodine content of seawater, which use a Technicon Auto-Analyser, is described. In both procedures the appropriate iodine species is first converted to iodate-iodine. Then, this is reacted with acid and excess iodide to give the iodonium ion, I3?, which is detected spectrophotometrically. In the total-iodine procedure the pre-oxidation is accomplished using bromine water. In the iodate procedure a pre-oxidation step using iodine-water can be included. It is anticipated that this will be used to test for the presence of naturally occurring reducing agents in seawaters, which by their action on iodonium ions could lead to an underestimate in iodate concentration. Seawaters, particularly coastal and surface oceanic ones, are known to contain iodine-reducing substances. Therefore, the validity of results obtained through the iodometric method for iodate must remain in some doubt until these tests have been made. The use of this method on anoxic waters which contain sulphides appears to be a prime example of where caution should be observed. The iodate procedure, both with and without pre-oxidation, has been tested on approximately 50 samples of waters from the Eastern Pacific Ocean; these waters did not appear to contain significant amounts of reducing agents. In a similar study, it was found that there was no significant difference between the results obtained by the new total-iodine procedure and an earlier automatic catalytic one.  相似文献   

18.
Analyses of two years (1992 and 1993) of high-resolution sea surface temperature satellite images of the southern Mid Atlantic Bight (MAB), showed that unusually extensive overhang of shelf water occurs episodically, and coherently over along shelf distances of several 100 km. These episodes are dubbed overrunning of the Slope Sea by shelf water. The overrunning volume has a “face” and a “back” (southern and northern limit). It transports substantial quantities of shelf water southward, and does not retreat onto the shelf, but eventually joins the western edge of the Gulf Stream in the vicinity of Chesapeake Bay. The combined analyses of satellite imagery and various in situ data further demonstrated that the shelf waters overrunning the Slope Sea were not mere surface features but reached depths between 40 and 60 m. Results confirm previous concepts on shelf circulation, shelf–slope exchange and fate of shelf water. They also shed new light on shelf water budget: overrunning of the Slope Sea and southwest transport by upper slope current constitutes an important conduit for shelf water transport. Winter storms move the shelf–slope front, and with it shelf water, offshore to distances 10–40 km. The offshore displacement of shelf water can be related to the onshore veering of the Gulf Stream near Cape Hatteras, producing a blocking effect on the shelf circulation. Such a blocking effect of the southwestward flow of shelf water in the MAB appeared to be the reason for the overrunning of shelf water off New Jersey. In addition, the excess fresh water discharge from the St. Lawerence was also observed to be related to the overflow of shelf water off New Jersey.  相似文献   

19.
Dissolved organic matter (DOM) composition and dynamics in temperate shallow coastal bays are not well described although these bays may be important as local sources of organic carbon to ocean waters and are often sites of economically-important fisheries and aquaculture. In this study surface water samples were collected on a monthly to bi-monthly basis over two years from a mid-Atlantic coastal bay (Chincoteague Bay, Virginia and Maryland, USA). Dissolved organic carbon (DOC) concentrations and light absorbance characteristics were measured on sterile-filtered water, and high-molecular weight (> 1 kDa) dissolved OM (DOM) was isolated to determine stable isotope composition and molecular-level characteristics. Our time series encompassed both a drought year (2002) and a year of above-average rainfall (2003). During the dry year, one of our sites developed a very intense bloom of the brown tide organism Aureococcus anophagefferens while during the wet year there were brown tide bloom events at both of our sampling sites. During early spring of the wet year, there were higher concentrations of > 1 kDa DOC; this fraction represented a larger proportion of overall DOC and appeared considerably more allochthonous. Based upon colored dissolved organic matter (CDOM) and high-molecular weight DOM analyses, the development of extensive phytoplankton blooms during our sampling period significantly altered the quality of the DOM. Throughout both years Chincoteague Bay had high DOC concentrations relative to values reported for the coastal ocean. This observation, in conjunction with the observed effects of phytoplankton blooms on DOM composition, indicates that Chincoteague Bay may be a significant local source of “recently-fixed” organic carbon to shelf waters. Estimating inputs of DOC from Chincoteague Bay to the Mid-Atlantic Bight suggests that shallow productive bays should be considered in studies of organic carbon on continental shelves.  相似文献   

20.
Copper in a series of samples from the northwestern Atlantic has been determined by anodic stripping voltammetry (ASV) and atomic absorption spectrometry after preconcentration by cobalt—APDC coprecipitation. Samples from a transect across the continental shelf directly off the New York Bight showed a linear relationship between total copper and salinity (31–34‰) and less than 5% of the total copper was detectable by ASV. A slope water station showed less than 9% of the total copper to be ASV detectable in the upper 780m, below which the ASV detectable copper increased to 70% at 3000 m. The Sargasso Sea profiles showed less than 7% ASV detectable copper in the upper 150 m; the fraction of the total copper detected by ASV increased to about 80% of the total copper at greater depths. The reduced availability of copper to the ASV measurement in coastal waters and open ocean surface waters appears to be related to recent contact with waters where biological productivity occurs.  相似文献   

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