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1.
This study examines the distribution of leachable particulate iron (Fe) in the Columbia River, estuary, and near-field plume. Surface samples were collected during late spring and summer of 2004–2006 as part of four River Influence on Shelf Ecosystems (RISE) cruises. Tidal amplitude and river flow are the primary factors influencing the estuary leachable particulate Fe concentrations, with greater values during high flow and/or spring tides. Near the mouth of the estuary, leachable particulate Fe [defined as the particulate Fe solubilized with a 25% acetic acid (pH 2) leach containing a weak reducing agent to reduce Fe oxyhydroxides and a short heating step to access intracellular Fe] averaged 770 nM during either spring tide or high flow, compared to 320 nM during neap tide, low flow conditions. In the near-field Columbia River plume, elevated leachable particulate Fe concentrations occur during spring tides and/or higher river flow, with resuspended shelf sediment as an additional source to the plume during periods of coastal upwelling and spring tides. Near-field plume concentrations of leachable particulate Fe (at a salinity of 20) averaged 660 nM during either spring tide or high flow, compared to 300 nM during neap tide, low flow conditions. Regardless of tidal amplitude and river flow, leachable particulate Fe concentrations in both the river/estuary and near-field plume are consistently one to two orders of magnitude greater than dissolved Fe concentrations. The Columbia River is an important source of reactive Fe to the productive coastal waters off Oregon and Washington, and leachable particulate Fe is available for solubilization following biological drawdown of the dissolved phase. Elevated leachable Fe concentrations allow coastal waters influenced by the Columbia River plume to remain Fe-replete and support phytoplankton production during the spring and summer seasons.  相似文献   

2.
The spatial distributions of dissolved manganese and nutrients were examined in the Columbia River plume off Oregon and Washington during the summer of 2004 and 2005 as part of the River Influence on Shelf Ecosystems (RISE) program. Factors influencing the hydrochemical characteristics of the freshly formed and aged Columbia River plume were investigated. Hydrographic data and nutrient concentrations were used to delineate three distinct water sources for the Columbia River Plume: California Current surface water, coastal upwelled water, and Columbia River water. The warm, intermediate salinity, nutrient poor California Current water contains low levels of dissolved manganese (< 5 nM) and silicic acid (< 5 μM), and is depleted in nitrate. The cold, high salinity, nutrient rich, freshly upwelled water is highly variable (2–20 nM) in dissolved manganese and can be as high as  45 μM in silicic acid and  30 μM nitrate. The variable Columbia River has summer temperatures ranging from  13 to 24 °C, high silicic acid concentrations (ranging from  120 to 200 μM), and lower nitrate concentrations (ranging from  2 to 20 μM). During the summer, the concentrations of silicic acid and dissolved manganese can exceed 100 μM and 200 nM, respectively, in near-field Columbia River plumes. These values are markedly greater than those of surface coastal waters (even during upwelling conditions). As the plume advects and mixes, the concentrations of these two constituents remain relatively high within plume waters. The concentrations of dissolved manganese in the near-field plume vary with tidal amplitude, exhibiting much higher concentrations for a given salinity during spring tides than during neap tides. For example, the Columbia River plume at a salinity of 20 has a concentration of dissolved manganese of  240 nM during spring tides, as compared to only  60 nM during low amplitude tides. Silicic acid concentrations in the near-field plume remain relatively constant throughout the tidal month. Calculations indicate there is roughly an equivalent yearly delivery of dissolved manganese and silicic acid to the coastal waters off Oregon and Washington by upwelled waters and by the Columbia River plume.  相似文献   

3.
The influence of the Columbia River plume on the distributions of nitrate and iron and their sources to coastal and shelf waters were examined. In contrast to other large estuaries, the Columbia River is a unique study area as it supplies very little nitrate (5 μM) and iron (14–30 nM) at salinities of 1–2 to coastal waters. Elevated nitrate and dissolved iron concentrations (as high as 20 μM and 20 nM) were observed, however, in the near field Columbia River plume at salinities of 20. Surface nitrate concentrations were higher than observed in the Columbia River itself and therefore must be added by entrainment of higher nitrate concentrations from subsurface coastal waters. Tidal flow was identified as an important factor in determining the chemical constituents of the Columbia River plume. During the rising flood tide, nitrate and iron were entrained into the plume waters resulting in concentrations of 15 μM and 6 nM, respectively. Conversely, during the ebb tide the concentrations of nitrate and total dissolved iron were reduced to 0.3–3 μM and 1–2 nM, respectively, with a concomitant increase in chlorophyll a concentrations. As these plume waters moved offshore the plume drifted directly westward, over a nitrate depleted water mass (< 0.2 μM). The plume water was also identified to move southwards and offshore during upwelling conditions and nitrate concentrations in this far field plume were also depleted. Iron concentrations in the near-field Columbia River plume are sufficient to meet the biological demand. However, due to the low nitrate in the Columbia River itself, nitrate in the plume is primarily dependent on mixing with nitrate rich, cold, high salinity subsurface waters. Without such an additional source the plume rapidly becomes nitrate limited.  相似文献   

4.
During the first year of the Northeast Pacific GLOBEC program we examined the spatial distributions of dissolved and particulate organic carbon and nitrogen in the surface waters off the Oregon and Washington coasts of North America. Eleven east–west transects were sampled from nearshore waters to 190 km offshore. Hydrographic data and the distribution of inorganic nutrients were used to characterize three distinct water sources: oligotrophic offshore water, the Columbia River plume, and the coastal upwelling region inshore of the California Current. Warm, high salinity offshore water had very low levels of inorganic nutrients, particulate organic carbon (POC) and dissolved organic carbon (DOC). Warm, low salinity water in the Columbia River plume was relatively low in nitrate, but showed a strong negative correlation between salinity and silicate. The river plume water had the highest levels of total organic carbon (TOC) (up to 180 μM) and DOC (up to 150 μM) observed anywhere in the sampling area. Cold, high salinity coastal waters had high nutrient levels, moderate to high levels of POC and particulate organic nitrogen (PON), and low to moderate levels of DOC and dissolved organic nitrogen (DON). Each of these regions has characteristic C:N ratios for particulate and dissolved organic material. The results are compared to concentrations and partitioning of particulate and dissolved organic carbon and nitrogen in other regions of the North Pacific and North Atlantic Oceans.  相似文献   

5.
分别于2012年3月和7月对长江口及其邻近海域水体中溶解态铝的分布及其影响因素进行了研究,并在2012年3月至2013年11月期间对长江徐六泾进行了连续观测。结果表明,徐六泾溶解态铝在夏季出现最高值,在冬季呈现最低值,平均值分别为(313±130)nmol/L和(140±43)nmol/L,表现出与径流量相似的季节变化规律。受陆源输入变化的影响,长江口溶解态铝的浓度由近岸向外海逐渐降低,且呈现出明显的季节性差异,即7月明显高于3月。3月表、底层海水中溶解态铝的浓度范围分别为21~129 nmol/L和27~146 nmol/L,平均值分别为(49±21)nmol/L和(59±27)nmol/L;7月表、底层溶解态铝的浓度范围分别为6~332 nmol/L和9~252 nmol/L,平均值分别为(66±69)nmol/L和(83±74)nmol/L。在7月,表、底层溶解态铝呈现显著性差异,底层沉积物的再悬浮可能是造成差异的主要原因。调查结果表明,溶解态铝在长江口呈现出清除型行为,清除主要发生在咸淡水混合初期,初步计算出7月份溶解态铝的清除率约为55%。  相似文献   

6.
As part of a larger program focused on understanding the biogeochemistry of large river plumes, we participated in two expeditions during 2000 to sample the Mississippi River plume. Surface water samples were collected using a trace metal clean towed fish and analyzed for total dissolved Fe, organic Fe complexing ligands and their associated conditional stability constants. The ligands in the river plume have conditional stability constants (log K′FeL between 10.5 and 12.3 with an average of 11.2 and standard deviation of 0.6) very similar to ligands found in the open ocean. Comparison of high flow and low flow regimes indicates that variability in flow may be the main cause of the variability in Fe concentrations in the plume. The organic Fe complexing ligands are in greatest excess during a time of higher flow. These ligands are responsible for maintaining very high (5 nM) Fe concentrations throughout the plume. Due to complexation with these organic ligands, the concentration of Fe remains above the Fe-hydroxide solubility level until a salinity above 35 is reached where there appears to be a sink for Fe in the less productive waters. Therefore, Fe is transported a great distance from the river source and is available for biological utilization in the coastal zone.  相似文献   

7.
Water column samples have been collected in the outer channel of the Ferrol Ria (NW Spain) during four occasions over a tidal cycle. The objective was to study the exchange of dissolved and particulate Cd, Cu, Pb and Zn and particulate Al, Fe and Si between the ria and the adjacent coastal waters. This study provides the first extensive dataset on dissolved and particulate metal concentrations in the water column of a Galician ria. Typical concentrations of dissolved Cd (96 ± 31 pM), Cu (8 ± 4 nM), Pb (270 ± 170 pM) and Zn (21 ± 10 nM) were similar than in other European Atlantic shelf and coastal waters. The fraction of metals in the particulate phase followed the trend: Pb > Cu Zn > Cd. The outgoing water from the ria was enriched in dissolved and particulate Cu, Pb and Zn compared with incoming waters, whereas Cd concentrations were similar for both waters. The suspended particulate matter was composed of a mixture of marine and continental material. The latter end-member was found to arise from the metal-rich ria bed sediments, which is diluted by the dominant metal-poor marine end-member. The net output flux of Cu from the channel is balanced by the freshwater inputs to the ria, and the net Zn flux gave a positive output to coastal waters. For Pb, the net flux to the coastal waters is less than that input from the rivers, as a result of its particle reactivity and deposition in sediments. On the contrary, a net input flux of dissolved Cd from coastal waters was observed, highlighting the oceanic source of this metal in the Galician rias. Results from the budget calculations are in agreement with the differential geochemical behavior of these elements in coastal waters.  相似文献   

8.
The use of dissolved Al as a tracer for oceanic water masses and atmospheric dust deposition of biologically important elements, such as iron, requires the quantitative assessment of its sources and sinks in seawater. Here, we address the relative importance of oceanic versus atmospheric inputs of Al, and the relationship with nutrient cycling, in a region of high biological productivity in coastal Antarctica. We investigate the concentrations of dissolved Al in seawater, sea ice, meteoric water and sediments collected from northern Marguerite Bay, off the West Antarctic Peninsula, from 2005 to 2006. Dissolved Al concentrations at 15 m water depth varied between 2 and 27 nM, showing a peak between two phytoplankton blooms. We find that, in this coastal setting, upwelling and incorporation of waters from below the surface mixed layer are responsible for this peak in dissolved Al as well as renewal of nutrients. This means that changes in the intensity and frequency of upwelling events may result in changes in biological production and carbon uptake. The waters below the mixed layer are most likely enriched in Al as a result of sea ice formation, either causing the injection of Al-rich brines or the resuspension of sediments and entrainment of pore fluids by brine cascades. Glacial, snow and sea ice melt contribute secondarily to the supply of Al to surface waters. Total particulate Al ranges from 93 to 2057 mg/g, and increases with meteoric water input towards the end of the summer, indicating glacial runoff is an important source of particulate Al. The (Al/Si)opal of sediment core top material is considerably higher than water column opal collected by sediment traps, indicative of a diagenetic overprint and incorporation of Al at the sediment–water interface. Opal that remains buried in the sediment could represent a significant sink of Al from seawater.  相似文献   

9.
Dissolved and particulate lead were measured over an annual cycle (12 surveys between February 1998 and January 1999) in the Morlaix River estuary (Brittany, France). The concentrations were investigated in both the water column and the sediment of the river bottom in relation to hydrological conditions. In the water column, dissolved and particulate lead concentrations ranged from 0.1 to 4.4 nM and from 0.04 to 1.9 μmol g− 1, respectively. Lead concentrations in surface sediment varied from 0.04 to 0.19 μmol g− 1 and concentrations in the sediment pore water of the estuary were below the detection limit. Compared with the ranges known for pristine estuaries, concentrations of Pb in the water column of the Morlaix River estuary were found to be much higher. Concentrations of Pb also exceeded the lower range of those known for industrialized estuaries. Extensive agricultural activities in the drainage basin may be responsible for Pb levels above pristine conditions. Furthermore, the sediment appeared not to be contaminated. A mass balance was constructed quantifying all known sources and sinks for the Pb in the estuary. Riverine input accounts for most of the total annual metal flux. Burial in sediments was the major sink within the estuary, which acts as a trap especially for the particulate lead. The mass balance shows that the metal accumulation ranged between 414.6 and 446.0 kg year− 1.  相似文献   

10.
In this study, we present seasonal changes (monthly samples from September 2001 to August 2003) in the abundance and composition of dissolved and particulate amino acids, at one station in the lower Mississippi and Pearl Rivers (LA, MS: USA). Spatial changes over a 4-day transmit from river km 390 to river mouth (Head of Passes, LA) in the Mississippi River, and a two-day downstream sampling from Jackson (MS) to Stennis Space Center (MS) were also determined. Temporal data in the lower Mississippi River showed significantly lower concentrations of dissolved combined amino acids (DCAA, 0.8 to 2.2 μM) and dissolved amino acids in high molecular weight fraction (HMW DAA, 0.2–0.4 μM) than in the Pearl River (DCAA, 1.4–4.3 μM; HMW DAA, 0.4–1.4 μM). Dissolved free amino acids (DFAA) were significantly lower than DCAA in both rivers, and displayed minimal seasonal variability. DCAA, HMW DAA, and particulate amino acids (PAA) were generally higher during high-flow periods, which may have suggested dominance in terrestrial sources. Carbon-normalized yield of PAA (%C-PAA) was generally higher during low-flow conditions and positively correlated with chlorophyll-a (chl-a), reflective of in situ sources. Downstream variability in the lower Mississippi River showed stable DCAA concentrations, a decline in PAA (from 1.06 to 0.43 μM), and a gradual increase in mole percent of non-protein amino acids (%NPAA). This likely reflected bacterial degradation of phytoplankton biomass during falling discharge. Nitrogen-normalized yield of PAA (%N-PAA) was inversely correlated with PAA (R = − 0.7, n = 48), indicative of short-term sedimentation and resuspension events. Conversely, downstream decreases in DCAA and middle-reach peaks of PAA and %N-PAA in the Pearl River, likely resulted from photochemical degradation of DOM as well as algal production during base-flow conditions. The comparisons in abundance and composition of DAA and PAA in these different river systems provides important information on in situ nitrogen and carbon cycling as related to riverine inputs of organic matter to coastal ocean.  相似文献   

11.
Shelf break systems are highly dynamic environments. However little is known about the influence that benthic interactions and water mass mixing may have on vertical distributions of iron in these systems. Dissolved Fe (< 0.4 μm) concentrations were measured in samples from nine vertical profiles across the upper slope (150–2950 m water depth) at the Atlantic Ocean–Celtic Sea shelf break. Dissolved iron concentrations varied between less than 0.2 and 5.4 nM, and the resulting detailed section showed evidence of a range of processes influencing the Fe distributions. The near sea floor data were interpreted in terms of release and removal processes. The concentrations of dissolved Fe present in near seabed waters were consistent with release of Fe from in situ remineralisation of particulate organic matter at two upper slope stations, and possibly release from pore water upon resuspension on shelf. Lateral transport of dissolved iron was evident from elevated Fe concentrations in an intermediate nepheloid layer and its advection along isopycnals. Surface waters at the shelf break also showed evidence of vertical mixing of deeper iron-rich waters. These waters contained macronutrients that sustained primary productivity in these otherwise nutrient-depleted surface waters. The data also suggest some degree of stabilisation of relatively high concentrations of iron, presumably through ligand association or as colloids. This study supports the view that lateral export of dissolved iron to the interior of the ocean from shelf and coastal zones and may have important implications for the global budget of oceanic iron.  相似文献   

12.
Water and sediment samples were collected at Datong from June 1998 to March 1999 to examine seasonal changes in the transports of nitrogen (N) and phosphorus (P) from the Changjiang River (Yangtze River) to the East China Sea (ECS). Dissolved inorganic nitrogen (DIN; dominated by nitrate) concentration exhibited small seasonality, and DIN flux was largely controlled by water discharge. Dissolved inorganic phosphorus (DIP) concentration was inversely correlated with water discharge, and DIP was evenly delivered throughout a year. The transports of DIN and DIP from the Changjiang River were consistent with seasonal changes in nutrient distributions and P limitation in the Changjiang Estuary and the adjacent ECS. Dissolved organic and particulate N (DON and PN) and P (DOP and PP) varied parallel to water discharge, and were dominantly transported during a summer flood. The fluxes of DOP and particulate bioavailable P (PBAP) were 2.5 and 4 times that of DIP during this period, respectively. PBAP accounted for 12–16% of total particulate P (PP), and was positively correlated with the summation of adsorbed P, Al–P and Fe–P. Ca–P, the major fraction of PP, increased with increasing percent of CaCO3. The remobilization of riverine DOP and PBAP likely accounted for the summer elevated primary production in DIP-depleted waters in the Changjiang Estuary and the adjacent ECS. The Changjiang River delivered approximately 6% of DIN (1459 × 106 kg), 1% of DIP (12 × 106 kg), and 2% of dissolved organic and particulate N and P to the totals of global rivers. The construction of the Three Gorges Dam might have substantially reduced the particulate nutrient loads, thereby augmenting P limitation in the Changjiang Estuary and ECS.  相似文献   

13.
Dissolved and particulate trace metal concentrations (dissolved Fe, Zn, Cd, Co, Cu and Ni; particulate Fe, Mn and Al) were measured along two transects in the Ross Sea during austral summer of 1990. Total Fe concentrations in southern Ross Sea and inshore waters were elevated >3.5 times that of northern waters. Dissolved Zn, Cd and Co concentrations were lower by factors of 4.5, 3.5 and 1.6 in southern surface waters relative to northern waters. Dissolved Cu and Ni concentrations were similar in both areas. Elevated Fe concentrations coincided with areas of increased productivity, phytoplankton biomass and nutrient drawdown, indicating that Fe is an important factor controlling the location of phytoplankton blooms in the Ross Sea. Particulate concentrations of Fe, Mn and Al indicate two possible sources of iron to the Ross Sea, resuspension of continental shelf sediments and iron incorporated in annual sea ice and released with meltwaters.  相似文献   

14.
This study characterized stormwater plume development and associated phytoplankton dynamics in a coastal marine ecosystem through shipboard monitoring. We focused on plumes within Santa Monica Bay, California (USA), a coastal system that is subject to rapid pulses of untreated runoff from the urbanized watershed of Los Angeles during the winter rainy season. The physical, chemical, and biological signatures of stormwater plumes were tracked over time after each of 4 precipitation events ranging in magnitude from 1.5 cm to 9 cm. Low salinity surface plumes persisted in Santa Monica Bay for at least 2 to 5 days over spatial scales of up to 15 km. This is consistent with a 6-day residence time for surface water plume parcels, which was estimated from a drifter trajectory in the bay. Shipboard sampling and salinity measurements in the surf zone showed that plumes often persisted even longer nearshore. Plume waters were generally characterized by higher concentrations of dissolved nitrogen, colored dissolved organic matter, and higher light attenuation than non-plume waters. The magnitude of the effect of stormwater runoff on phytoplankton dynamics was dependent on the size of each storm and subsequent residence time of runoff within the bay. Rain events led to increases in primary productivity, phytoplankton biomass, and specifically, increases in diatom biomass, as measured by concentrations of biogenic silica.  相似文献   

15.
River plumes have important effects on marine ecosystems. Variation in the extent and dispersal of river plumes is often associated with river discharge, wind characteristics and ocean circulation. The objectives of this study were to identify the Tokachi River plume by satellite, determine its relationship with river discharge and clarify its temporal and spatial dynamics. SeaWiFS multispectral satellite data (normalized water-leaving radiance: nLw) with 1.1 km spatial resolution were used to determine the spatial and temporal variability of the plume during 1998–2002. Supervised maximum likelihood classification using six channels of nLw at 412, 443, 490, 510, 555 and 670 nm with each band's spectral signature statistic was used to define classes of surface water and to estimate the plume area. Supervised maximum likelihood classification separated three to four classes of coastal water based on optical characteristics as a result of wind stress events. The satellite-observed plume area was correlated with the amount of river discharge from April to October. The plume distribution patterns were influenced by wind direction and magnitude, the occurrences of a near-shore eddy field and surface currents. Empirical orthogonal function (EOF) was used to express the spatial and temporal variability of the plume using anomalies of nLw(555) monthly averaged images. The first mode (44% of variance) showed the turbid plume distribution resulting from re-suspension by strong wind mixing along the coast during winter. This mode also showed the plume was distributed along-shelf direction in spring to early autumn. The second mode (17% of variance) showed spring pattern across-shelf direction. EOF analysis also explained the interannual variability of the plume signature, which might have been affected by the flow of the Oyashio Current and the occurrence of a near-shore eddy field.  相似文献   

16.
河口羽流是河口冲淡水在陆架中扩展的主要形式, 其扩展受到诸多动力与地形因素的影响, 口门拦门沙就是其中之一。以一个理想化的河口为例, 采用区域海洋模型(regional ocean modelling system, ROMS), 研究口门拦门沙对河口羽流扩展的影响, 具体包括拦门沙对羽流的出流状态、扩展范围以及远场区沿岸流淡水输运的影响。研究结果表明, 拦门沙增加了口门处的水体分层, 减小了羽流出流速度, 增大了羽流凸出体的半径, 减小了远场区沿岸流宽度, 并进而减少了沿岸流中的淡水输送。本项研究对地形因素对河口羽流的扩展研究以及陆源物质的向海输运等均具有重要意义。  相似文献   

17.
Aerosol (soluble and total) iron and water-column dissolved (DFe, < 0.2 μm) and total dissolvable (TDFe, unfiltered) iron concentrations were determined in the Canary Basin and along a transect towards the Strait of Gibraltar, in order to sample across the Saharan dust plume. Cumulative dust deposition fluxes estimated from direct aerosol sampling during our one-month cruise are representative of the estimated deposition fluxes based on near surface water dissolved aluminium concentrations measured on board. Iron inventories in near surface waters combined with flux estimates confirmed the relatively short residence time of DFe in waters influenced by the Saharan dust plume (6–14 months). Enhanced near surface water concentrations of DFe (5.90–6.99 nM) were observed at the Strait of Gibraltar mainly due to inputs from metal-rich rivers. In the Canary Basin and the transect towards Gibraltar, DFe concentrations (0.07–0.76 nM) were typical of concentrations observed in the surface North Atlantic Waters, with the highest concentrations associated with higher atmospheric inputs in the Canary Basin. Depth profiles showed that DFe and TDFe were influenced by atmospheric inputs in this area with an accumulation of aeolian Fe in the surface waters. The sub-surface minimum of both DFe and TDFe suggests that a simple partitioning between dissolved and particulate Fe is not obvious there and that export may occur for both phases. At depths of around 1000–1300 m, both regeneration and Meddies may explain the observed maximum. Our data suggest that, in deep waters, higher particle concentrations likely due to dust storms may increase the scavenging flux and thus decrease DFe concentrations in deep waters.  相似文献   

18.
Stormwater plumes in the southern California coastal ocean were detected by MODIS-Aqua satellite imagery and compared to ship-based data on surface salinity and fecal indicator bacterial (FIB) counts collected during the Bight'03 Regional Water Quality Program surveys in February–March of 2004 and 2005. MODIS imagery was processed using a combined near-infrared/shortwave-infrared (NIR-SWIR) atmospheric correction method, which substantially improved normalized water-leaving radiation (nLw) optical spectra in coastal waters with high turbidity. Plumes were detected using a minimum-distance supervised classification method based on nLw spectra averaged within the training areas, defined as circular zones of 1.5–5.0-km radii around field stations with a surface salinity of S < 32.0 (“plume”) and S > 33.0 (“ocean”). The plume optical signatures (i.e., the nLw differences between “plume” and “ocean”) were most evident during the first 2 days after the rainstorms. To assess the accuracy of plume detection, stations were classified into “plume” and “ocean” using two criteria: (1) “plume” included the stations with salinity below a certain threshold estimated from the maximum accuracy of plume detection; and (2) FIB counts in “plume” exceeded the California State Water Board standards. The salinity threshold between “plume” and “ocean” was estimated as 32.2. The total accuracy of plume detection in terms of surface salinity was not high (68% on average), seemingly because of imperfect correlation between plume salinity and ocean color. The accuracy of plume detection in terms of FIB exceedances was even lower (64% on average), resulting from low correlation between ocean color and bacterial contamination. Nevertheless, satellite imagery was shown to be a useful tool for the estimation of the extent of potentially polluted plumes, which was hardly achievable by direct sampling methods (in particular, because the grids of ship-based stations covered only small parts of the plumes detected via synoptic MODIS imagery). In most southern California coastal areas, the zones of bacterial contamination were much smaller than the areas of turbid plumes; an exception was the plume of the Tijuana River, where the zone of bacterial contamination was comparable with the zone of plume detected by ocean color.  相似文献   

19.
The aim of this study was to investigate the cycling of dissolved inorganic and organic nutrients using moored instrumented buoys (SmartBuoys) during the spring bloom in the North Sea. The instrumentation on the buoys enabled high frequency measurements of water-column integrated irradiance and in situ chlorophyll to be made, and also preserved water sample collection which were used for dissolved inorganic and organic nutrient analyses. The SmartBuoys were located in the year-round well-mixed plume zone associated with the River Thames and in the summer stratified central North Sea. These site locations allowed comparison of nutrient concentrations and cycling, and spring bloom development at two contrasting sites. The spring bloom was expected to be initiated at both stations due to increasing insolation and decreasing suspended load leading to higher water-column integrated irradiance. Due to differences in suspended load between the sites, the spring bloom started ∼2 months earlier in the central North Sea. The spring bloom in the Thames plume also resulted in higher maximum phytoplankton biomass due to the higher pre-bloom nutrient concentrations associated with riverine input. The use of SmartBuoys is also shown to allow the cycling of dissolved organic nutrients to be examined over the critical, and often undersampled, spring bloom period. Dissolved Organic Nitrogen (DON) clearly increased during the spring bloom in the central North Sea compared to winter concentrations. DON also increased in the Thames plume although showing greater winter variability related to higher riverine and sedimentary dissolved organic matter input at this shallow (∼18 m) coastal site. DON increase during the spring bloom was therefore related to primary production at both sites probably due to active release by phytoplankton. At both stations DON decreased to pre-bloom concentrations as the bloom declined suggesting the released DON was bioavailable and removed due to heterotrophic uptake and production. The preserved nutrient samples from the central North Sea site were also suitable for Dissolved Organic Phosphorus (DOP) analysis due to their low suspended load with similar trends and cycling to DON, albeit at lower concentrations. This suggested similar processes controlling both DON and DOP. The variable timing of short term events such as the spring bloom makes sampling away from coastal regions difficult without the use of autonomous technology. This study demonstrates for the first time the applicability of using preserved samples from automated buoys for the measurement of dissolved organic nutrients.  相似文献   

20.
Concentrations of cobalt (Co) in surface waters from the Sagami River to northern Sagami Bay and from the Yura River to southwestern Wakasa Bay in Japan were determined in order to investigate the factors governing the distribution of this metal during estuarine mixing. Dissolved (<0.2 μm) and particulate (>0.2 μm) Co showed non-conservative mixing behavior with low or mid-salinity maxima within those two estuarine regions, indicating benthic remobilization and/or sewage input apart from riverine input during the estuarine mixing. These results are supported by a suite of complementary measurements of other parameters, such as manganese, phosphate, and suspended particulate matter concentrations. In addition, the concentration ratio of dissolved Co to total Co (dissolved plus particulate) increased along the salinity gradient, implying the potential for desorption of this metal from suspended particulate matter on estuarine mixing.  相似文献   

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