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1.
Chromophoric dissolved organic matter (CDOM) is the major light absorber in the Baltic Sea. In this study, excitation emission matrix (EEM) fluorescence spectra and UV–visible absorption spectra of CDOM are reported as a function of salinity. Samples from different locations and over different seasons were collected during four cruises in 2002 and 2003 in the Baltic Sea in both Pomeranian Bay and the Gulf of Gdansk. Absorption by CDOM decreased with increased distance from the riverine source and reached a relatively stable absorption background in the open sea. Regression analysis showed that fluorescence intensity was linearly related to absorption by CDOM at 375 nm and aCDOM(375) absorption coefficients were inversely related to salinity. Analysis of CDOM-EEM spectra indicated that a change in composition of CDOM occurred along the salinity gradient in the Baltic Sea. Analysis of percent contribution of respective fluorophore groups to the total intensity of EEM spectra indicated that the fluorescence peaks associated with terrestrial humic components of the CDOM and total integrated fluorescence decreased with decreasing CDOM absorption. In contrast, the protein-like fraction of CDOM decreased to a lesser degree than the others. Analysis of the percent contribution of fluorescence peak intensities to the total fluorescence along the salinity gradient showed that the contribution of protein-like fluorophores increased from 2.6% to 5.1% in the high-salinity region of the transect. Fluorescence and absorption changes observed in the Baltic Sea were similar to those observed in similar transects that have been sampled elsewhere, e.g. in European estuaries, Gulf of Mexico, Mid-Atlantic Bight and the Cape Fear River plume in the South Atlantic Bight, although the changes in the Baltic Sea occurred over a much smaller salinity gradient.  相似文献   

2.
The release of ammonium from the photochemical degradation of dissolved organic matter (DOM) has been proposed by earlier studies as a potentially important remineralisation pathway for refractory organic nitrogen. In this study the photochemical production of ammonium from Baltic Sea DOM was assessed in the laboratory. Filtered samples from the Bothnian Bay, the Gulf of Finland and the Arkona Sea were exposed to UVA light at environmentally relevant levels, and the developments in ammonium concentrations, light absorption, fluorescence and molecular size distribution were followed. The exposures resulted in a decrease in DOM absorption and loss of the larger sized fraction of DOM. Analysis of the fluorescence properties of DOM using parallel factor analysis (PARAFAC) identified 6 independent components. Five components decreased in intensity as a result of the UVA exposures. One component was produced as a result of the exposures and represents labile photoproducts derived from terrestrial DOM. The characteristics of DOM in samples from the Bothnian Bay and Gulf of Finland were similar and dominated by terrestrially derived material. The DOM from the Arkona Sea was more autochthonous in character. Photoammonification differed depending on the composition of DOM. Calculated photoammonification rates in surface waters varied between 121 and 382 μmol NH4+ L− 1 d− 1. Estimated areal daily production rates ranged between 37 and 237 μmol NH4+ m− 2 d− 1, which are comparable to atmospheric deposition rates and suggest that photochemical remineralisation of organic nitrogen may be a significant source of bioavailable nitrogen to surface waters during summer months with high irradiance and low inorganic nitrogen concentrations.  相似文献   

3.
Absorption and fluorescence of chromophoric dissolved organic matter (CDOM) and dissolved organic carbon (DOC) measurements were performed during three oceanographic surveys in 1994 in the southern Baltic Sea (Polish area of the Baltic Proper). DOC was measured both by high-temperature catalytic oxidation (HTCO) and low-temperature oxidation (LTO) conventional persulphate methods. CDOM fluorescence was shown to be highly correlated with absorption, with the same regression parameters, despite the seasonal change in different hydrographic conditions and the fluorescence quantum yield variations (1.23 ± 0.07 in April and 0.97 ± 0.12 in September). The results show a good correlation between the optical parameters and DOC although ˜ 70% of the DOC does not display significant absorption in the UV-visible range (350–750 nm). The non-absorbing DOC measured with HTCO method appears unaffected by seasonal changes. Consequently, total DOC can be predicted by optical methods using remote sensing techniques. The non-absorbing DOC measured by LTO method varies from 62% (April) to 76% (September), which implies that there is requirement for estimates on a seasonal basis.  相似文献   

4.
The optical properties and distribution of dissolved organic matter in the surface waters of the Kara Sea and bays of Novaya Zemlya archipelago were studied during the 63th cruise of the R/V Akademik Mstislav Keldysh. The fluorescence of dissolved organic matter has been studied over wide excitation (230–550 nm) and emission (240–650 nm) wavelength ranges. Based on the results of fluorescence measurements, we propose a simple technique for estimating the relative content of humic compounds entering the Kara Sea shelf region with Ob and Yenisei river runoff. We have found that the blue shift parameters of the DOM fluorescence are Δ270–310 = 28 ± 2 nm and Δ355–310 = 29 ± 2 nm. The highest contents of humic compounds in surface waters were measured on the transect across the desalinated layer of the Kara Sea, near the continental slope on the transect along the St. Anna Trough, and in the area of Sedova, Oga and Tsivol’ki bays. Traces of labile terrigenous organic matter were found in the region of the Voronin Trough, in the bays of the Severny Island of Novaya Zemlya, as well as in some freshwater reservoirs and ice samples of the archipelago. We established a conservative distribution of dissolved organic matter, whose content in water varied from 1.25 to 8.55 mg/L.  相似文献   

5.
A new method for the characterization of chromophoric colloidal organic matter in seawater has been applied to samples from the Baltic Sea, Kattegatt and Skagerrak seas. Size fractionation of the sample by Flow Field-Flow Fractionation and measurement of the fluorescent and UV absorbing properties of the individual size fractions result in a relative molar mass distribution (RMM) of the optical properties. The RMM distributions have been used to estimate number and weight average relative molar masses, and polydispersity indices. At least two sources of coloured organic matter were identified from the ratio of fluorescence to UV: the Baltic surface water and the Skagerrak deep water. The dominating processes were mixing and dilution, but processes such as photo bleaching of fluorescence are also believed to be important. The RMM distribution derived from UV detection (1150–1300 Dalton) increased with increasing salinity while that derived for fluorescence (1500–1250 Dalton) decreased with increasing salinity. The specific UV absorbance taken as a proxy of the aromaticity of the chromophoric organic material showed decreasing trend with both increasing salinity and increasing UV derived weight average relative molar mass. Increasing polydispersity of the colloidal material was also observed as a function of salinity.  相似文献   

6.
Absorbance at 360 nm and dissolved organic carbon (DOC) concentration were measured on 47 filtered water samples collected from streams and rivers of the west coast of South Island, New Zealand. The regression equation (DOC (g m‐3) = 59.6 Abs1 cm + 1.9) calculated from the data, reliably predicted DOC concentration within the range 1.6–43.2 gm‐3. This relationship is similar to that found fsr some Venezuelan and south‐eastern United Stales waters indicating that it may have widespread utility for estimating DOC concentrations in soft waters where DOC is dominated by humic substances  相似文献   

7.
This study addresses sources and diagenetic state of early-season dissolved organic matter (DOM) in the Northeast Water Polynya (NEWP) area northeast of Greenland from distributions of humic substance fluorescence (HSfl), dissolved organic carbon (DOC), and dissolved organic nitrogen (DON) in the water column inside and outside the NEWP area. The water masses of the polynya area had acquired their spring/summer temperature–salinity characteristics at the time of sampling, and also had individual, different DOM signatures. DOC concentrations were variable within and among water masses in the polynya area, indicating patchy local sources and sinks of DOC. PySW and polynya intermediate water (PyIW) had higher average DON concentrations and average lower C:N ratios than polynya bottom water (PyBW), indicating a larger fraction of fresh DOM in PySW and PyIW than in PyBW. Ice-covered, polynya area surface waters (PySW) had higher DOC concentrations (113±14 μM, n=68) than surface water (SW) outside the polynya area (96±18 μM, n=6). The DOM C:N ratios in a low-salinity, ice-melt subgroup of PySW samples indicate labile material, and these low-salinity surface waters appeared to have a local DOC and DON source. In contrast, HSfl was significantly lower inside than outside the NEWP area. Despite the lower HSfl values within the NEWP area, the PySW values were high when compared to open-ocean water. There were no local terrestrial sources for HSfl to the NEWP area and the East Greenland Current is therefore proposed as a likely source of allochtonous HSfl. When HSfl was used as a conservative tracer, up to 70% of the water in PySW and PyIW was found to be derived from SW, which contains a high fraction of water from the East Greenland Current. Similarly, a mixing model based on HSfl indicated that 80% of early-season DOC and 90–100% of early-season DON in PySW and PyIW were derived from SW, indicating a potentially high fraction of terrestrially-derived, relatively refractory DOM in the early-season NEWP area.  相似文献   

8.
The contribution of organic matter (humic compounds) to the alkaline reserve of seawater in the Sea of Japan, in the Razdol’naya River estuarine waters, and in the interstitial waters of the sediments of the Sea of Okhotsk was characterized using two procedures for alkalinity measurements: the method by Bruevich and that of the sample equilibrium with air. It was found that the surface waters of the Sea of Japan contained about 20 μmol/kg of alkalinity of organic origin, and this value twofold decreased with depth. For most of the actual cases of the calculations of the seawater carbonate system, this value may be neglected. Meanwhile, the contribution of organic alkalinity to the Razdol’naya River waters amounts to nearly 120 μmol/kg. It was shown that, if this value in the calculation of the carbonate system of the Razdol’naya River estuary-Amur Bay is neglected, this may cause gross errors in the values of the partial pressure of carbon dioxide (the error might be over 1500 μatm) and in the dissolved inorganic carbon (an error over 150 μmol/kg). The maximum absolute contribution of the humic matter (over 300 μmol/kg) was found for the interstitial waters in selected sediments of the Sea of Okhotsk. In the interstitial waters of these sediments, humic matter concentrations as high as 300 mg/l were detected. The data obtained show that the determination of the amount of humic matter must be an indispensable condition for an adequate analysis of estuarine carbonate systems and of the interstitial water in reduced marine sediments.  相似文献   

9.
The fluorescence of dissolved organic matter in seawater   总被引：3，自引：0，他引：3  
A total of 28 vertical profiles of seawater fluorescence was measured in the Sargasso Sea, the Straits of Florida, the Southern California Borderlands, and the central Pacific Ocean. In all cases, surface seawater fluorescence was low as a result of photochemical bleaching which occurs on the timescale of hours. Fluorescence of deep water was 2–2.5 times higher than that of surface waters, and was constant, implying a long residence time for fluorescent organic matter, possibly of the order of thousands of years. Fluorescence correlates well with nutrients (NO3−, PO43−) in mid-depth waters (100–1000 m) in the Sargasso Sea and the central North Pacific, consistent with results in the central Pacific and the coastal seas of Japan. This suggests that regeneration or formation of fluorescent materials accompanies the oxidation and remineralization of settling organic particles.The various sources and sinks of fluorescent organic matter in the global oceans are assessed. The major sources are particles and in situ formation; rivers, rain, diffusion from sediments, and release from organisms are minor sources. The major sink is photochemical bleaching.  相似文献   

10.
The distribution and characteristics of coloured dissolved organic matter (CDOM) in the Baltic – North Sea transition zone were studied. The aim was to assess the validity of predicting CDOM absorption in the region on the basis of water mass mixing alone and demonstrate the utility of CDOM as an indicator of water mass mixing in coastal seas. A three-end-member mixing model representing the three major allochthonous CDOM sources was sufficient to describe the patterns in CDOM absorption distribution observed. The three-end-member water masses were the: Baltic outflow, German Bight and the central North Sea. Previously, it was thought that water from the German Bight transported northwards in the Jutland coastal current only sporadically influenced mixing between the Baltic and North Sea. The results from this study show that water from the German Bight is detectable at salinities down to 12 in the Kattegat and Belt Sea. On average, 23% of the CDOM in bottom waters of the Kattegat, Great Belt, Belt Sea, Arkona Sea and the Sound originated from the German Bight. Using this conservative mixing model approach, local CDOM inputs were detectable but found to be limited, representing only 0.25% of CDOM in the surface waters of the Kattegat and Belt Sea. The conservative mixing of CDOM makes it possible to predict its distribution and characteristics and offers a powerful tool for tracing water mass mixing in the region. The results also emphasize the need to include the Jutland Coastal current in hydrodynamic models for the region.  相似文献   

11.
Suspended particulate matter samples were collected from the water column, the bottom nepheloid layer and the ‘ fluffy layer ’ from four stations along a coastal-basin transect in the Pomeranian Bight, western Baltic Sea. Sampling was performed nine times between October 1996 and December 1998 for various analyses, including electron probe x-ray micro analysis for detailed mineralogical investigations.Specific vertical patterns of clay mineral distributions were found. Suspended particulate matter (SPM) in the bottom nepheloid layer and the ‘ fluffy layer ’ overlying sediments was enriched in organic carbon and hydrated three layer clay minerals, whereas the non-aggregated SPM was dominated by quartz and biogenic opal. It appears that separation effects operate during aggregation of mineral particles and organic matter in repeated cycles of resuspension and settling. No clear seasonal variations in the composition of the SPM were found, in spite of high spatial and temporal variability of biological and physical variables. The results suggest that preferential incorporation, possibly aided by microbiological colonization, of hydrated three layer silicates into the organic flocs is a process that occurs under a wide range of conditions. Because aggregates sink faster than individual particles, aggregate formation led to a relative enrichment of illite and smectite in the near-bottom layers. Considering the affinity of organic contaminants and heavy metals to organic matter, the selective removal of aggregated organic matter and hydrated three-layer clay minerals from the water column and enhanced transport in the near-bottom fluffy layer may be a natural cleansing mechanism operating in the shallow waters of the bight.  相似文献   

12.
Data is presented for the concentrations of organic carbon and nitrogen, and C:N ratios, in marine particulate matter, and for POC and PN, from surface waters collected in the northeastern Atlantic, South Atlantic, Indian Ocean and China Sea.The organic carbon content of this particulate matter varies between 4.6% and 29.9%, and has an average of 17.8%. The average organic carbon content of particulate matter from the various oceans decreases in the order: Northeastern Atlantic > South Atlantic > Indian Ocean > China Sea.The nitrogen content of the particulate matter varies between 1.0% and 3.9%, with an average of 2.2%, and in general follows the same trend as that of organic carbon.C:N ratios vary between 5.1 and 10.6, and have an average of 7.9.The POC contents of the oceanic waters vary between 6.6 and 211 μg/l, with an average of 52 μg/l. The concentrations in the surface waters decrease in the following order: Northeastern Atlantic τ China Sea > South Atlantic > Indian Ocean.The concentrations, and compositions, of particulate matter from various coastal localities are given for comparison with the oceanic values.  相似文献   

13.
Dissolved organic nitrogen (DON), dissolved organic carbon (DOC) and inorganic nutrient concentrations were determined in samples from an area encompassing the Northeast Water Polynya from June to August 1993. In June, still ice-covered polynya area surface waters (PySW) had significantly higher (p<0.05) DOC concentrations (110 μM, n=68) than surface water outside the polynya area (96 μM, n=6). Melting ice and ice algae are suggested as DOC sources. DOC concentrations found in this study are consistent with other studies showing higher DOC concentrations in the Arctic than in other ocean areas. As the productive season progressed, DOC concentrations in Polynya surface water (PySW) decreased (p<0.05) from 110 to 105 μM, while DON concentrations increased (p<0.05) from 5.6 to 6.1 μM, causing a significant decrease (p<0.05) in the C : N ratios of DOM from spring (C : N ratio 20) to summer (C : N ratio 17). We found a significant (p<0.05) decrease in the DOM C : N ratio in all water masses within the polynya area as the productive season progressed. DON was the largest fraction of total dissolved nitrogen (TDN) in PySW and surface waters outside the polynya area. TDN was calculated as the sum of DON, nitrate, nitrite and ammonium concentrations. DON increased (p<0.05) from 62% to 73% of TDN in PySW from spring to summer, a result of increasing DON concentrations and decreasing inorganic nitrogen concentrations over the productive season. The seasonal accumulation of DON and the corresponding decrease in nitrate concentrations in waters with primary production indicate that it is important to take the DON pool into account when estimating export production from nitrate concentration decreases in surface waters. PySW TDN concentrations decreased (p<0.05) from 9.1 (n=61) to 8.6 μM (n=60) from spring (May 25 through June 19) to summer (July 1 through July 27). The seasonal decrease in surface water TDN concentrations corresponded to increases in TDN concentrations in deeper water masses within the Polynya. Most of the TDN increase in deep water was in the form of DON. A possible explanation is that PON was dissolved (partially remineralized) in the water column at mid depths, causing increases in the DON concentration. Transfer of N from PySW (with a short residence time in the polynya area) to Polynya Intermediate Water and deep waters of the Norske and Westwind Trough with multi-year residence times keeps N from leaving the polynya area. In spring, nutrients from degradation of OM in PyIW could support primary production. The role of PyIW as an OM trap could be important in supporting primary production in the polynya area.  相似文献   

14.
依据2017年8—9月对黄海海域溶解有机物(DOM)的调查，探讨了夏季黄海海水中溶解有机碳(DOC)和有色溶解有机物(CDOM)的空间分布特征。在表层海水中，受陆源影响较大的近岸海域CDOM含量相对较高，北黄海冷水团区域由于水产养殖的饵料引起DOC浓度升高，且该部分DOC以无色为主。DOC浓度随深度逐渐降低，而CDOM逐渐升高，该特征在冷水团区域更为显著，因此DOC和CDOM在冷水团区域的表底差异远大于浅水区的非冷水团区域。陆源输入和初级生产是引起表层DOC升高的主要原因，而光漂白则引起CDOM降低，同时光漂白还导致表层水体中CDOM分子量和芳香性低于底层。底层溶解氧饱和度在冷水团为80%～93%，均表现为弱不饱和状态。层化不仅阻碍了O2向底层水体输送，还抑制了DOC和CDOM的垂向混合，这是引起冷水团区域表底层DOC和CDOM差异较大的主要原因。  相似文献   

15.
Bacterial biomass and production rate were measured in the surface (0–100 m) and mesopelagic layers (100–1,000 m) in the subarctic Pacific and the Bering Sea between July–September, 1997. Depth profiles were determined at stations occupied in oceanic domains including the subarctic gyres (western, Bering Sea, and Gulf of Alaska) and a boundary region south of the gyres. In the surface layer (0–100 m), both bacterial biomass and production were generally high in the western and Bering Sea gyres, with the tendency of decrease toward east. This geographic pattern was consistent with the dominant regime of phytoplankton biomass at the time of our survey. A significant portion of variation in bacterial production was explained by the concentration of chlorophyll a (r 2 = 0.340, n = 60, P < 0.001) and, to the greater extent, by the concentration of semilabile total organic carbon (SL-TOC = TOC at a given depth—TOC at 1,000 m, r 2 = 0.488, n = 59, P < 0.0001). Temperature significantly improved the regression model: temperature and chlorophyll jointly explained 60% of variation in bacterial production. These results support the hypothesis that bacteiral growth is largely regulated by the combination of temperature and the supply of dissolved organic carbon in subarctic surface waters. In the mesopelagic layer (100–1,000 m), the geographic pattern of bacterial production was strikingly different from the surface phytoplankton distribution: the production was high in the boundary region where the phytoplankton biomass was lowest. Bacterial growth appeared to be largely controlled by the supply of organic carbon, as indicated by the strong dependency of bacterial production on SL-TOC (r 2 = 0.753, n = 75, P < 0.0001). The spatial uncoupling between surface phytoplankton and mesopelagic bacterial production suggests that the supply rate of labile dissolved organic carbon in the mesopelagic zone does not simply reflect the magnitude of the particulate organic carbon flux in the subarctic Pacific.  相似文献   

16.
An analysis of the variations in the concentrations of 137Cs and 90Sr radionuclides in the Baltic Sea surface waters after the accident at the Chernobyl nuclear power plant was performed. An instability of the 137Cs concentration values during the short-term observations was found, when these values were differed 2-to 3-fold. The concentrations of 90Sr appeared to be more stable; meanwhile, their deviations sometimes exceeded the ranges of the experimental errors. By the variations in the monthly average values of the radionuclide concentrations in the surface waters of the Baltic Sea in 1989–1995, no trend of the water self-purification was observed. The theoretical results obtained confirmed the potential of the formation and propagation of patches with increased concentrations of 137Cs in the southeastern part of the Baltic Sea. The most reliable factor that controlled the process of self-purification of the Baltic Sea water appeared to be the mean annual value of the concentration of radionuclides. Pronounced divergences were obtained between the measured and calculated mean annual concentrations of 137Cs and 90Sr radionuclides in the surface waters of the Baltic Sea in 1989–2001. These divergences are explained by the potential influence of the waters from the Gulf of Bothnia and by other additional supplies of radionuclides to the marine environment, which were not included into the mathematical models.  相似文献   

17.
The absorption coefficient of chromophoric dissolved organic matter (aCDOM) has been found to be correlated with fluorescence emission (excitation at 355 nm). In the coastal European Atlantic area and in the Western Mediterranean Sea (Gulf of Lions), a significant statistical dependence has been found between aCDOM and fluorescence with dissolved organic carbon (DOC) concentration. The relationship shows that, in the river plume areas (Rhine in the North Sea and Rhône in the Gulf of Lions), a consistent fraction of DOC (from 40% to 60% of the average of the DOC measured) is non-absorbing in visible light range, where the dissolved organic matter (DOM) is typically absorbent. In comparison, in the open sea, apparently not affected by the continental inputs, the entire DOC belongs to the chromophoric DOM whose specific absorption is lower (5 to 10 times) than that found in the river plume areas.  相似文献   

18.
The concentration distribution was studied for dissolved oxygen, phosphorus forms, and particulate matter in Curonian Bay of the Baltic Sea in poorly known consolidated ice cover conditions during the winter seasons of 2010, 2011, and 2013. The surface and near-bottom waters were sampled at 51 stations. The ice cover exerts no significant effect on the typical seasonal variation of all considered parameters in the basin. The concentrations of mineral and organic phosphorus in the bay appeared to be lower by factors of 2–4 compared to summer values. A two- to threefold decrease in the concentrations of organic phosphorus since 2010 to 2011 and then to 2013 was recorded in the bay, which resulted from a decrease in phosphorus production by phytoplankton. Despite water being isolated from air by ice, the absence of wave mixing, and the decrease in oxygen production owing to the seasonal winter decrease in the intensity photosynthetic processes, no oxygen deficiency was found in the basin. This is because oxygen supplied to the bay by river runoff and production by photosynthesis in the bay exceed the utilization for oxidation of organic matter resulting from low bioproductivity of the waters during winter. The winter decrease in the fraction of biogenic particulate matter is seen as a four- to sevenfold drop in its total concentration in the waters compared to summer seasons. The absence of wave roiling of bottom sediments also caused a decrease in the secondary supply of biogenic particulate matter from sediments into near-bottom waters. No negative trends of geoecological conditions in the bay were revealed by the studied parameters under consolidated ice cover conditions.  相似文献   

19.
高原湖泊溶解有机质的三维荧光光谱特性初步研究   总被引：9，自引：0，他引：9  
提要近年来,荧光光谱技术被广泛应用于研究天然水体中溶解有机质(Dissolved Organic Matter,DOM)的物理化学特性。为了理解高原湖泊中DOM的组成、荧光光谱特性及其在湖泊水体中的垂直分布情况,作者利用荧光发射光谱、三维荧光光谱研究云贵高原湖泊红枫湖和百花湖中的DOM。结果显示,高原湖泊DOM主要表现为类富里酸荧光,包括可见区和紫外区两种类型的荧光峰,各种天然水体中都有报道的类蛋白荧光在红枫湖DOM中并不明显,而在百花湖DOM中则有较强的类蛋白荧光。溶解有机质所含三种类型荧光峰(PeakA:紫外区类富里酸荧光峰;PeakB:可见区类富里酸荧光峰;PeakC:类蛋白荧光峰)的荧光强度与溶解有机碳之间没有明显的线性相关关系,可能与高原湖泊水体pH值、DOM在湖泊不同深度由于受到光降解、微生物降解等作用存在差异等因素有关。与有机质结构和成熟度有关的荧光峰比值r(A,C)在1.40—2.09范围内,红枫湖南湖、百花湖DOM样品的r(A,C)值随着水体深度有下降的趋势,而红枫湖北湖DOM的r(A,C)值则随着水体深度有较大起伏,揭示了高原湖泊水体中DOM的结构以及分布情况存在差异。另外,r(A,C)值与pH之间具有良好的正相关关系,其相关系数红枫湖南湖DOM为0.95,百花湖两个采样点DOM分别为0.67、0.75,而红枫湖北湖DOM则显示出一定的负相关性(R2=0.45)。  相似文献   

20.
Marine colloidal material (1 kDa–0.2 μm) was isolated by cross-flow ultrafiltration followed by diafiltration and freeze-drying from surface waters of the Gulf of Mexico and the Middle Atlantic Bight (MAB), as well as from estuarine waters of Galveston Bay. Elemental characterization of isolated colloidal material included organic carbon (OC) and selected trace metal (Cu, Pb, Zn, Cd, Co, Ni, Cr, Be, Fe, Al, Mn, V, Ba, and Ti) determinations. It was found that levels of these metals in marine colloids ranged from <0.1 to 50 μg/g colloidal matter, except for Fe which generally had a concentration >120 μg/g. Most metals (Cu, Pb, Zn, Ni, Al, Mn, V, and Ti) had an average concentration >1 μg/g while concentrations of Cd, Co and Be were usually <1 μg/g. Metal concentrations (μg/g) in isolated colloids were, in general, higher in Galveston Bay than in the Gulf of Mexico, suggesting either high abundance of trace metals in estuarine waters or differences in organic matter composition. Higher colloidal metal concentrations in the MAB than in the Gulf of Mexico might be due to higher terrestrial inputs in the MAB. Colloidal metal concentrations (μg/g) were generally lower than those in average soils, continental crust and suspended particles. However, metal/aluminum ratios (Me/Al) in isolated marine colloids were significantly higher than those for average soils and continental crust. Most importantly, colloids had a metal composition and metal/OC ratio (Me/C) similar to humic substances and marine plankton, suggesting that marine colloids largely originate from planktonic sources and are composed of predominately organic components. The Me/C ratios of Galveston Bay colloids followed the sequence of Cu>Ni, Cr, Zn>Mn>Co>Pb, Cd, which is similar to the Irving–Williams order except for Mn, suggesting that the interaction of metals with marine colloids is determined by the affinity of metals for specific organic ligands.  相似文献   

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