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1.
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2.
Concentrations of lead were measured in a surface transect and at two vertical profile stations (15°N and 20°S) in the Central Pacific. These measurements complement similar measurements made earlier in the North Pacific at 33°N and in the Northwest Atlantic at 34°N [1,2], as well as recent measurements of eolian lead input fluxes near each of these locations [3]. The new transect of surface water concentrations of lead corroborates previous measurements, which decrease from 13 ng/kg at 30°N to 4 ng/kg at 17°S in the Central Pacific [4]. This transect gradient is shown to overlie a similar geographic gradient of subsurface maximum concentrations of lead in the three Pacific vertical profile stations, decreasing from 14 ng/kg at 33°N to 11 ng/kg at 14°N to 2.5 ng/kg at 20°S. Lead concentrations at each of those locations exhibit maxima at 400 m, decreasing concentrations to 2500 m and approximately concentrations of 0.8–1.1 ng/kg below that depth. The subsurface maximum at the northwest Atlantic profile station (36 ng/kg at 34°N) is also congruent with surface water lead concentrations which decrease from 806 ng/kg to 32 ng/kg in an offshore transect from Rhode Island to 34°N, 66°W [5], and the shape of the Atlantic profile is congruent with those in the Pacific. There is a positive correlation between the magnitudes of eolian lead input fluxes and the magnitudes of the upper water maxima in lead concentration profiles at corresponding locations as follows: South Pacific easterlies 3 ng/cm2 yr vs. 2.5 ng/kg; North Pacific easterlies 6 ng/cm2 yr vs. 11 ng/kg; North Pacific westerlies 50 ng/cm2 yr vs. 14 ng/kg; and North Atlantic westerlies 170 ng/cm2 yr vs. 36 ng/kg.This relationship enables one to view the anthropogenic perturbations of the marine lead cycle on a global scale, since the industrial origin of eolian and seawater lead has been established by correlations between geographic patterns of industrial lead emissions to the atmosphere and isotopic ratios of industrial leads [3] and by geographic patterns of Pb/silicate-dust ratios and lead isotopic ratios in ocean surface waters [3–5]. These new data coupled with earlier biogeochemical data indicate that surface water concentrations of lead in the North Pacific and North Atlantic are now conservatively estimated to be 8 to 20-fold greater and those in the South Pacific are 2-fold greater than natural concentrations because of industrial emissions of lead to the atmosphere.  相似文献   

3.
Particulates amounting to 0.1–2.0 g efficiently collected from large volumes of Atlantic and Pacific surface waters have been analyzed for carbonate, opal, quartz and several natural and man-made radioisotopes.The concentrations of particles range between 10 and 600 μg/kg. In the equatorial regions particle concentrations are low and similar in both the oceans. At higher latitudes (>30°N or S), the Atlantic waters, however, have higher concentrations of particles compared to those in the Pacific. The latitudinal distribution exhibits a north-south symmetry with higher concentrations in the 30°–60° belt. Based on the particulate abundance for CaCO3 and opal and their sedimentation, we have estimated their production and in-situ integrated dissolution rates for a few regions.Radioisotopes having different source functions, namely14C and239Pu injected due to nuclear weapon tests,234Th,230Th and228Th produced in-situ in seawater,232Th which derives primarily from land,210Pb introduced via wet precipitations and226Ra introduced through diffusion from deep-sea sediments have been measured in the particulates. The relative enrichment factors for these nuclides in particles vary as Th ? Pu > Pb > Ra. The atmospheric bomb fallout pattern is discernible in the surface particulates; the239Pu concentration increases with latitude in both the hemispheres; however, the values are about a factor of two lower in the southern hemisphere.The distribution pattern of radioisotopes is found to be complex, even for234Th whose source function in the oceans is uniform. In view of the differences in the source functions it becomes possible to delineate the principal geochemical/geophysical processes which determine the concentrations of these nuclides in surface waters.  相似文献   

4.
The iodine content of marine suspended matter obtained from thirteen stations in the Atlantic between 75°N and 55°S has been measured. The concentration of particulate iodine is high in the surface, up to 127 ng/kg of seawater being observed. Below the euphotic zone, it drops sharply to 1–2 ng/kg. The iodine-containing particles are probably biogenic. A simple box-model calculation shows that only 3% of the particulate iodine produced in the surface water may reach the deep sea and that the residence time of these particles in the surface water is about 0.1 year.  相似文献   

5.
Water samples collected at the 21°N hydrothermal site on the East Pacific Rise crest, including Deep-Tow and hydrocast samples collected in 1977 and three hot vent water samples collected recently with the submersible “Alvin”, contain significant additions of3He,4He, and Mn. Although the vent water collections were at least 50-fold diluted with ambient seawater, they are up to 53 times enriched in3He and 7.4 times enriched in4He relative to saturated seawater, with concentrations of total dissolvable manganese (TDM) up to 310 μg/kg.3He and4He covary in the vent samples, with3He/4He about 8 times the atmospheric ratio, reflecting a mantle helium source. In contrast to the helium isotopes the Mn/3He ratio in the vent samples is variable, ranging from 4.3 × 104 up to 1.0 × 105 g/cm3. Profiles of3He/4He and TDM in the water column at 21°N show a sharp maximum ofδ(3He) = 47%and TDM= 0.69 μg/kg, much higher than the average values of 34% and 0.2 μg/kg for the deep water in this region. This spike in3He and Mn occurs at 2400 m depth, 200 m above the level of the 21°N vents, and 100 m higher than any local bathymetry, evidence for upward transport of the hydrothermal discharge via rising plumes of hot vent water. Two of the 21°N Deep-Tow samples associated with small (?0.010°C) temperature anomalies hadδ(3He) = 38%and TDM= 0.28 and 0.58 μg/kg, also slightly elevated relative to background. The Deep-Tow and hydrocast samples have lower Mn/3He ratios than average vent samples due to Mn removal by scavenging. Comparison of vent samples and water column measurements at 21°N indicate that the pure vent water could be detected using3He and Mn even when diluted ～105 times with seawater, confirming that these two tracers are extremely sensitive indicators of submarine hydrothermal activity.  相似文献   

6.
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7.
The distribution of “ash” (the non-combustible fraction of marine suspended matter) and concentrations of particulate Al, Ca, Fe, Cr, Ni, Cu, Sr and234Th in surface waters and of210Pb,230Th and234Th in two vertical profiles (385–4400 m) of the Indian Ocean are reported.The ash concentrations in surface waters follow the primary productivity pattern, with higher abundances in samples south of 40°S and lower concentrations in the equatorial and subtropical regions. Opaline silica and CaCO3 are the dominant components of the ash in samples from >40°S and from 7°N to 39°S, respectively. Aluminosilicates are only a minor constituent of the surface particulate matter. The metal/Al ratios in the surface particles are significantly higher compared to their corresponding crustal ratios for all the metals analyzed in this work. Comparison of enrichment factors between marine aerosols, plankton and surface oceanic particles, seem to indicate that this high metal/Al ratio in surface particles most likely arises from their involvement in marine biogeochemical cycles. Particulate234Th activity in surface waters parallels the ash abundance implying that its scavenging efficiency from surface waters depends on the particulate concentration.The particulate230Th and210Pb concentration profiles increase monotonously with depth. It is difficult to ascribe this increase to a process other than the in-situ vertical scavenging of230Th and210Pb from the water column by settling particles. The mean settling velocities of particles calculated from the particulate230Th data using a one-dimensional settling model is about 2 × 10?3 cm/s. The settling velocity computed from the particulate230Th profiles does not appear to be compatible with the particulate210Pb depth profiles; one possible explanation to account for the disparity would be that230Th and210Pb are scavenged by different size populations of particles.On the whole, the geographic distribution of particulate matter, their composition and settling velocities in the Atlantic, Pacific and Indian Oceans are similar indicating that they are controlled by quite similar processes in the marine hydrosphere.  相似文献   

8.
The Batu Hijau copper–gold mine on the island of Sumbawa, Indonesia operates a deep-sea tailings placement (DSTP) facility to dispose of the tailings within the offshore Senunu Canyon. The concentrations of trace metals in tailings, waters, and sediments from locations in the vicinity of the DSTP were determined during surveys in 2004 and 2009. In coastal and deep seawater samples from Alas Strait and the South Coast of Sumbawa, the dissolved concentrations of Ag, As, Cd, Cr, Hg, Pb and Zn were in the sub μg/L range. Dissolved copper concentrations ranged from 0.05 to 0.65 μg/L for all depths at these sites. Dissolved copper concentrations were the highest in the bottom-water from within the tailings plume inside Senunu Canyon, with up to 6.5 μg Cu/L measured in close proximity to the tailings discharge. In general, the concentrations of dissolved and particulate metals were similar in 2004 and 2009.  相似文献   

9.
Sea floor hydrothermal activity in the Guaymas Basin, Gulf of California, is quite different from that associated with ridge crest spreading centers. Injection of hydrothermal fluids occurs in the bottom of a semi-enclosed basin and water column anomalies produced by this activity increase to much higher values than in the open ocean. In the Guaymas Basin the hydrothermal venting generates large clouds of fine suspended particulate matter (SPM) 100–300 m above active mounds and chimneys. These hydrothermal clouds have potential temperature anomalies of about 0.010–0.020°C, are enriched in dissolved silica, particulate manganese, and depleted in dissolved oxygen relative to areas away from the vents. The particulate manganese values increase from about 3 nmol/kg at ～ 1000 m, well above the enclosing topography of the subsill basin, to 100–150 nmol/kg in the clouds of SPM and in the bottom nepheloid layer. The particulate Mn in the hydrothermal clouds appears to originate from both direct precipitation of dissolved Mn2+ injected by the vents and entrainment of Mn-rich SPM in the rising hydrothermal plumes. Injection of silica-rich vent fluids into the basin bottom waters produces a silica anomaly of 10–15 μmol relative to the other deep basins of the Gulf of California. Spillover of Guaymas Basin deep water produces a silica plume just above the basin sill depth which is detectable to the mouth of the Gulf. A simple two-endmember mixing model indicates that the deep waters of the Guaymas Basin contain approximately 0.1% hydrothermal fluid. Oxygen anomalies associated with the hydrothermal clouds are on the order of 5 μmol relative to regions away from active vents. The basin as a whole shows a depletion in oxygen of about 13 μmol relative to the other deep basins of the Gulf. The mixing model shows that this oxygen consumption can be explained by the oxidation of dissolved sulfide and methane injected by the hydrothermal vents. Box models of the deep basins of the southern Gulf of California indicate that the Guaymas Basin has a significantly higher source term for dissolved silica and sink term for dissolved oxygen than the other basins. The calculated flux of hydrothermal fluids into the Guaymas Basin is 10–12 m3/s.  相似文献   

10.
Surface transects and vertical profiles of total and leachable particulate Fe, Mn, Al and P, along with dissolved and soluble Fe were obtained during August 2003 in the southeastern Bering Sea. High concentrations of leachable particulate Fe were observed in the bottom waters over the Bering Sea shelf with an unusually high percentage of the suspended particulate Fe being leachable. Leachable particulate Fe averaged 81% of total particulate Fe, and existed at elevated concentrations that averaged 23 times greater than dissolved Fe in the isolated cool pool waters over the mid shelf where substantial influence of sedimentary denitrification was apparent. The elevated leachable particulate Fe is suggested to be a result of sedimentary Fe reduction in surficial sediments, diffusion of Fe(II) from the sediments to the bottom waters, and subsequent oxidation and precipitation of reduced Fe in the overlying bottom waters. Eddies and meanders of the Bering Slope Current can mix this Fe-rich water into the Green Belt at the outer shelf-break front. Elevated levels of leachable particulate Fe were observed in surface waters near the Pribilof Islands where enhanced vertical mixing exists. Storm events and/or cooling during fall/winter with the resultant destruction of the thermally stratified two-layer system can also mix the subsurface water into surface waters where the elevated leachable particulate Fe is a substantial source of biologically available Fe.  相似文献   

11.
Ten samples were recovered by the submersible “Cyana” submersible from two groups of hydrothermal vents located 2600 m deep along the East Pacific Rise at 13°N. The maximum measured temperature was 317°C and minimum pH 3.8. A systematic determination of major and trace elements has been carried out and mixing lines between a high-temperature component (HTC) and seawater are observed. The water chemistry of the HTC slightly differs for several elements at the two sites. This HTC is deprived of SO4 and Mg and is greatly enriched in most other species. Maximum concentrations are (in units per kg):Cl = 0.72mol; Br = 1.1mmol; Na = 0.55mol; K = 29mmol; Rb = 14 μmol; Ca = 52mmol; Sr = 170 μmol; Mn = 750 μmol; Fe = 1mmol; Al = 15 μmol; Si = 21mmol. For many elements, the magnitude of the anomaly relative to seawater does not compare with the results obtained from the Galapagos or East Pacific Rise 21°N. The enrichment of cations relative to seawater is likely related to the huge Cl excess through charge balance. TheBr/Cl ratio is close to that for seawater. However, it is not clear whether the Cl excess is due to gas release or basalt hydration (formation of amphibole chlorite or epidote).P-T dependence of SiO2 solubility suggests that water-rock interaction last occurred at a depth in excess of 1 km below the sea floor. A mixing line of87Sr/86Sr vs. Mg/Sr demonstrates that the HTCs have a nearly identical87Sr/86Sr ratio of 0.7041 for both sites. A water/rock ratio of about 5 is inferred, which differs from the 1.5 value obtained at 21°N.  相似文献   

12.
Particulate and soluble,210Pb activities have been measured by filtration of large-volume water samples at two stations in the South Atlantic. Particulate phase210Pb (caught by a 0.4-μm filter) varies from 0.3% of total210Pb in equatorial surface water to 15% in the bottom water. The “absolute activity” of210Pb per unit mass of particulate matter is about 107 times the activity of soluble210Pb per unit mass of water, but because the mass ratio of particulate matter to water is about 10?8, the particulate phase carries only about 10% of the total activity. In Antarctic surface water the particulate phase carries 40% of the total210Pb activity; the absolute activity of this material is about the same as in other water masses and the higher fraction is due to the much larger concentration of suspended matter in surface water in this region.In the equatorial Atlantic the particulate phase210Pb activity increases with depth, by a factor of 40 from surface to bottom, and by a factor of 4 from the Antarctic Intermediate Water core to the Antarctic Bottom Water. This increase with depth is predicted by our previously proposed particulate scavenging model which indicated a scavenging residence time of 50 years for210Pb in the deep sea. A scavenging experiment showed that red clay sediment removes all the210Pb from seawater in less than a week. The Antarctic particulate profile shows little or no evidence of scavenging in this region, which may be due to the siliceous nature of the particulate phase in circumpolar waters. Our previous observation that the210Pb/226Ra activity ratio is of the order of 0.5 in the deep water is further confirmed by the two South Atlantic profiles analyzed in the present work.  相似文献   

13.
Determinations of dissolved reactive and total dissolved mercury, particulate and sedimentary mercury, dissolved organic carbon (DOC), particulate organic carbon (POC) and suspended particulate matter (SPM) have been made in the estuary of river Douro, in northern Portugal. The estuary was stratified by salinity along most of its length, it had low concentrations of SPM, typically <20 mg dm(-3), and concentrations of DOC in the range <1.0-1.8 mg dm(-3). The surface waters had a maximum dissolved concentration of reactive mercury of about 10 ng dm(-3), whereas for the more saline bottom waters it was about 65 ng dm(-3). The surface waters had maximum concentrations of total suspended particulate mercury of approximately 7 microg g(-1) and the bottom waters were always <1 microg g(-1). Concentrations of mercury in sediments was low and in the range from 0.06 to 0.18 microg g(-1). The transport of mercury in surface waters was mainly associated with organic-rich particulate matter, while in bottom waters the dissolved phase transport of mercury is more important. Lower particulate organic matter, formation of chlorocomplexes in more saline waters and eventually the presence of colloids appear to explain the difference of mercury partitioning in Douro estuarine waters.  相似文献   

14.
14C specific activities in the western Atlantic show aging of about 160 years between 42°N and 30°S for southward-moving North Atlantic Deep Water. Most of the aging occurs in the North Atlantic, with a small increase in14C level for abyssal water near the equator.The northward-flowing Antarctic Bottom Water component ages about 80 years between 50°S and the equator. The rate of Atlantic bottom water formation is estimated at 18 Sverdrups; the rate of flow for northward-moving Antarctic Bottom Water at about 6 Sverdrups.  相似文献   

15.
Barite particles are a universal component of suspended matter in the Atlantic and Pacific Oceans. This is demonstrated by scanning electron microscope and electron microprobe analyses of samples collected during the GEOSECS program. These discrete particles, about 1 μm in diameter, account for by far the greatest part of the total particulate barium of most of the filters collected at different depths. Total particulate barium (mean value: 20 ng/kg seawater) was measured on the same filters by instrumental neutron activation analysis.Several observations indicate that biochemical, rather than purely chemical, processes are involved in the formation of the BaSO4 mineral in the water column. Sr/Ba molar ratios among the individual barite grains, particularly from surface waters are extremely variable, which would not be anticipated for purely chemical interactions. Barite crystals occurring within fecal debris have been observed throughout the water column. Within such debris decomposition of the abundant organic matter may provide the micro-environment predicted as necessary for the precipitation of BaSO4. Finally, a strong correlation between nutrient content and particulate barium is found in the upper 1000 m of the water column, which also suggests a control of barite formation by biota.Some of the barite dissolves at depth in the water column. Dissolution rates were calculable for two GEOSECS stations, from which a dissolved barium flux of 0.4 μg/cm2 yr was deduced. This figure is of the same order as the dissolved barium flux calculable from the barium content and known dissolution rates of calcareous and siliceous tests: approximately 0.5 μg/cm2 yr. These fluxes represent the largest source of dissolved barium in the water column, the other being river input (0.6 μg/cm2 yr). This supports the contention that the barium in the water column is mostly recycled. The residual flux of barite-Ba reaching the sea floor is of about equal importance as the flux of barium associated with fast-settling fecal material. These two sources together are almost sufficient to account for the total sedimentation rate of barium.  相似文献   

16.
Measurements of five cosmogenic32Si vertical profiles in Atlantic waters (27°N to 60°S) are presented. The amounts of dissolved SiO2 extracted range from 2 to 54 g; the amounts of water from which SiO2 was extracted range between 540 kg and 270, 000 kg. In additon, SiO2 recovered from four surface particulate composites (64°N to 61°S) were also analyzed for32Si.32Si measurements were made by milking and counting the daughter activity, 32P. The net32P activities range from 0.7 to 6.8 cph; typical errors in measurements of the32P activities are 20–30%.The32Si concentrations vary from 0.6 dpm/106 kg of water in the North Atlantic surface waters to 235 dpm/106 kg at 400 m depth in the circumpolar waters. The vertical profiles of32Si at the five Atlantic stations approximately follow the Si profiles but the depth gradients are different. This would be expected also considering the in-situ release mechanisms due to dissolution and advection/diffusion from the bottom waters. Except for the circumpolar station 89, where the Si and32Si profiles show the effect of marked vertical mixing (nearly depth independent profiles), the profiles show the following features: (1) specific activities of32Si (32Si/SiO2 ratios) are lowest at intermediate depths, and (2) on an average the surface specific activities are higher, by 2–4 times, than the bottom water values. These data are consistent with generation of the highest specific activity32Si waters at the surface, where Si concentrations are lowest and precipitation adds cosmogenic32Si scavenged from the troposphere. Rapid removal of biogenic silica to the water-sediment interface, without much dissolution during transit, leads to the second regime of high32Si specific activities.The32Si inventories in the water column in the latitude belt 27°N-27°S are in the range (1–1.4) × 10−2 dpm32Si/cm2, which is consistent with the expected fallout of cosmogenic32Si. However, the32Si column inventories south of 40°S are higher by a factor of 5–7, whereas the corresponding Si inventories increase by only a factor of 3. This excess32Si in the Southern Ocean cannot be explained by direct fallout from the stratosphere or by melting of Antarctic snow and ice. Instead, this excess is maintained primarily by the southward deep-water transport of32Si dissolved from sinking particulates.  相似文献   

17.
Dissolved copper concentrations at five stations in the eastern Atlantic between 20 and 24°N are presented. The metal is depleted in surface waters with concentrations ranging from 1.1 to 1.7 nmol/l. Marked increases in concentration were found in near-bottom waters with levels up to 10.9 nmol/l; these are attributed to the release of dissolved copper from the surface sediment.  相似文献   

18.
13C and ΣCO2 data from the North and South Atlantic, the Antarctic, and the North and South Pacific are given. The δ13C of the ΣCO2 in the deep water (～3000m) decreases from 1.7‰ in the North Atlantic to ?0.10‰ in the North Pacific. This change is attributed to the addition of about 158 μmoles of CO2 per kg of seawater. The in-situ oxidation of organic matter accounts for 83% of this increase in ΣCO2, while the remainder is attributed to dissolution of calcium carbonate.The δ13C of the dissolved CO2 in mid-latitude surface water samples is controlled by a quasi-steady-state equilibrium with atmospheric CO2 at a mean temperature of 16°C. The δ13C and ΣCO2 values of Antarctic surface water samples suggest that these waters are derived from a mixture of North Atlantic deep water and equilibrated surface water.  相似文献   

19.
We present the distribution of226Ra in eight vertical profiles from the eastern Pacific. The profiles are located along a meridional trend near 125°W, from 43°S to 29°N. Surface226Ra concentrations are about 7 dpm/100 kg, except for the two stations south of 30°S where the higher values are due to the Antarctic influence. Deep waters show a distinctive south-to-north increase in the226Ra content, from about 26 to 41 dpm/100 kg near the bottom. Unlike in the Atlantic and Antarctic Oceans, the effect of226Ra injection from bottom sediments is clearly discernible in the area. The presence of this primary226Ra can be traced up to at least 1–1.5 km above the ocean floor, making this part of the sea bed among the strongest source regions for the oceanic226Ra. Numerical solutions of a two-dimensional vertical advection-diffusion model applied to the deep (1.2–4 km)226Ra data give the following set of best fits: upwelling velocity(Vz) = 3.5m/yr, vertical eddy diffusivity(Kz) = 0.6cm2/s, horizontal (north-south) eddy diffusivity(Ky) = 1 × 107cm2/s, and water-column regeneration flux of226Ra(J) = 3.3 × 10?5dpmkg?1yr?1 as an upper limit. These parametric values are in general agreement with one-dimensional (vertical) model fits for the Ra-Ba system. However, consideration of226Ra balance leads us to suspect the appropriateness of describing the vertical exchange processes in the eastern Pacific with constantVz and Kz. If future modeling is attempted, it may be preferable to treat the area as a diffusion-dominant mixing regime with depth-dependent diffusivities.  相似文献   

20.
Surface waters collected along the salinity gradient of the Hudson River estuary in four cruises between 1995 and 1997 were size-fractionated into particulate (>0.45 μm), ‘dissolved' (<0.45 μm), colloidal (10 kDa, 0.45 μm) and low molecular weight (<10 kDa) phases. Dissolved Cd concentrations (range: 0.11–1.19 nM) in surface waters of the estuary appear to have decreased fourfold (from an average of 2.36 to 0.61 nM) over a 23-year period, since the initial analysis of samples collected in the 1970s by Klinkhammer and Bender [Estuar. Coastal Shelf Sci. 12 (1981) 629–643]. This interannual decline reflects improvement in sewage treatment and the elimination of industrial Cd sources to the Hudson River estuary. In contrast, dissolved Mn levels (range: 0.033–1.46 μM) have remained relatively constant over the same period of time, suggesting that anthropogenic sources have very limited impact on Mn concentrations in the estuary. The concentrations of both Cd and Mn appeared to strongly depend on the season and/or river discharge. The highest concentrations were detected under low freshwater discharge, implying that limited hydraulic flushing allows a build-up of metals in the water column. Although the decline in Cd levels within the estuary reflects a reduction in the magnitude of anthropogenic inputs, mass balance estimates indicated that current sources of Cd to the estuary include sewage discharges (in the lower estuary around Manhattan) and diagenetic remobilization from industrial Cd deposited in sediments nearly 2 decades ago (in the upper estuary near Foundry Cove). Moreover, under low river discharge, the sources considered in our model (sewage, riverine input, atmospheric deposition, and benthic fluxes) could account for no more than 60% of the Cd exported from the lower estuary to the ocean. This suggests that undefined sources such as ground water and inputs from other watersheds (e.g., Long Island Sound and Newark Bay) may potentially influence the water quality of the New York Harbor. The size-fractionated metal concentrations indicated that most of the traditionally defined ‘dissolved' Cd and Mn consisted of <10 kDa molecular weight species. High molecular weight colloidal species of Mn accounted for about 50% of the dissolved fraction at the riverine end-member and <5% at intermediate and high salinities. Colloidal Cd accounted for <6% of the dissolved phase throughout the estuary. Unlike the non-conservative excess (relative to ideal dilution of river water and seawater) of dissolved Mn observed along the estuary, high molecular weight colloidal Mn appeared to be removed at the head of the estuary. The small contribution of colloidal Cd and Mn to the ‘dissolved' phase suggests that remobilization from suspended particulate phases and/or from sediments occurs through the formation of small molecular weight species.  相似文献   

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