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1.
The molecular size distribution of humic substances has been investigated in two recent sediment samples of different ages taken from a single core sample collected off Walvis Bay, south-west Africa. Extractable humic acids were found to be by far the major form of organic carbon in both sediments, the near-surface younger sample containing predominantly high molecular weight (>100 000 molecular weight) humic acids and little fulvic acids whilst the deeper, older sample contained relatively less humic acid and relatively more fulvic acid of a range of molecular weights. A significant age difference was found between the >300 000 molecular weight and the <30 000 molecular weight fractions of the near-surface sample, the lower molecular weight fraction being older than the higher molecular weight fraction.The data suggest that in this rapidly accumulating, organic-rich sediment the first step en route from the planktonic matter to the humic complexes is direct and rapid incorporation of the biogenic material into high molecular weight humic acids.  相似文献   

2.
Recent experimental evidence concerning the chemical forms of zinc occurring in sea water is reviewed in order to aid in the systematic understanding of zinc geochemistry in the marine environment. The review indicates the necessity of systematizing the results obtained by different methods for the determination of zinc in sea water with respect to the chemical nature of the zinc fractions measured. Analytical procedures for the zinc determinations in sea water by spectrophotometry with dithizone extraction and anodic stripping voltammetry with composite mercury graphite electrodes are described. By using these methods, various pre-treatment tests were carried out to relate the results of different modes of measurements to the chemical forms of zinc involved. The comparisons of the results of these tests lead to an estimation of the occurrence of the following categories of chemical forms of zinc in sea water: (1) ionic plus labile form, (2) inorganic complexes and colloids as well as weak organic complexes and (3) occuled fraction in large organic molecules and/or organic colloids. Capabilities of different analytical procedures for differentiating one category from another are discussed.  相似文献   

3.
北极孔斯峡湾表层沉积物中溶解有机质的来源与转化历史   总被引：7，自引：0，他引：7  
在北极地区孔斯峡湾采集28个表层沉积物样品,测定了其中水溶性有机质(也称溶解有机质,DOM)的分子量分布、紫外/可见吸收光谱和三维荧光光谱特征,并利用平行因子分析(PARAFAC)模型对DOM的荧光组分和来源进行了解析。结果表明:孔斯峡湾表层沉积物中有色溶解有机质(CDOM)及其中的荧光溶解有机质(FDOM)含量均从内湾向外湾方向呈逐渐累积的趋势,但CDOM中的FDOM所占比例逐渐减小,与DOM趋于老龄化密切相关。沉积作用减弱以及长期的光化学降解和微生物降解作用对此起主要贡献,并导致腐殖质和小分子组分在沉积物DOM中所占的比例呈逐渐递增的趋势。沉积物DOM包含陆源类腐殖质、自生源类腐殖质和类蛋白等三个荧光组分,但是其组成比例空间差异很大。吸收光谱斜率比(SR)随自生源所占百分比增加而减小,随DOM腐殖质组分中陆源与自生源的比值增加而增加;腐殖化指数(HIX)随类腐殖质与类蛋白质比值和水深的增加而增加,生物源指数(BIX)随自生源比例增加而增加。峡湾沉积物DOM的组成和来源存在着高度的空间差异,在冰川湾区由水体颗粒有机质(POM)的近期转化和迁移而来,而在峡湾中央及口门附近以较老的腐殖质为优势,主要源于水体DOM长期迁移和转化。研究表明,FDOM/CDOM,SR,HIX和BIX等构成的CDOM光谱指纹信息可以作为揭露沉积物溶解有机质来源及迁移转化历史的工具,对探索海洋与冰川相互作用影响下的峡湾环境演变有着重要意义。  相似文献   

4.
In this paper the chemical characteristics of humic substances (humic acid and fulvic acid) from East China Sea surficial sediment are studied through combination of chemical and physical methods. Results show that humic acids have less aromatic hydrocarbon and more alkane structure.The contents of amino acids from hydrolyzate of humic substances are different. The amount of various amino acids (such as acidic, neutral or basic amino aicd) of fulvic acid is higher than that of humic acid. The distribution order of amino acid abundance in various kinds of sediments is neutral amino acid>aromatic amino acid> basic amino acid.In addition, mathematical statistic method is also used to study their distribution. All samples show similar regularities, i. e., the contents of glycine, alanine, aspartic and glutamic are very high and those of cystine and methionine are very low or even disappear.The above results further confirm that humic acid and fulvic acid have similar composition and structure.  相似文献   

5.
本文采用元素分析、镜下观察、红外光谱、扫描电镜和热解分析等技术,分析了冲绳海槽柱状样中腐植酸、富里酸和干酪根的化学、物理特征,并探讨了它们之间的成因关系和干酪根类型。沉积物的产烃能力甚差,每吨沉积物仅能生成0.49～1.18kg烃类物质。  相似文献   

6.
Determination of total chromium on two profiles and chromium III on four samples of equatorial Pacific Ocean water have been carried out using coprecipitation of chromium from sea water with hydrous iron oxides, followed by ion-exchange separation and isotope dilution mass spectrometry. Results for two Pacific profiles show increasing total chromium concentration from surface to 250 m. The Cr concentration appears to be different below 1,000 m, with nearly homogeneous concentrations for the first profile and regularly increasing Cr concentrations from 0.330 to 0.550 μg/l at 3,900 m for the second one. Results for Cr(III) show that trivalent species are dominant in these samples.  相似文献   

7.
《Oceanologica Acta》1998,21(5):645-654
Intensity and spectral characteristics of the fluorescence of water samples collected along the transect Cherbourg-Isle of Wight during four cruises for excitations at 370, 313 and 270 nm have been investigated within the framework of the FluxManche II program. Seasonal and spatial differences appeared to reflect on the one hand, variations in terrestrial inputs, and on the other hand, waters masses structuring. The observed linear variation of the fluorescence intensity with salinity indicates a gradual dilution of the continental humic material in going from the coasts to the central part of the English Channel. The largest signal was observed for the English coastal waters in agreement with important terrestrial inputs from the Solent river. While the fluorescence intensity was not found to be correlated with the DOC, it shows a good correlation with the nutrients. This result could indicate both a supply from terrestrial inputs and an almost simultaneous autochtonous regeneration. As similarly reported for waters in the eastern part of the French coastal zone, excitation at 313 nm gives evidence for the presence of two classes of fluorescent dissolved organic matter. These two fluorescent components are indicative of the simultaneous presence of continental humic substances and substances whose assignment to marine humic substances or to heterotrophic related substances are still an open question. As compared to the eastern part of the Channel along the French coasts, excitation at 270 nm indicates a lower content of protein-like compounds which may be related to a lower biological activity along the transect or may be due to the fact that the samplings were made out of the phytoplanktonic bloom period (April–May 1995).  相似文献   

8.
Molecular weight and trace metal distributions of fulvic and humic acid fractions of marine sediments from the Seto Inland Sea were investigated by using a gel filtration technique in combination with atomic absorption and emission spectrometries. A binary molecular weight distribution was found both in the fulvic acid fraction and in the humic acid fraction. The fulvic acid fractions with molecular weights of less than 1.5×103 and of 5×103?104 accounted for 38–57 % and 25–41 % of the total fulvic acids, respectively, and the humic acid fractions with molecular weights of 102?104 and of over 2×105 accounted for 58–73 % and 16–27 % of the total humic acids, respectively. The components with molecular weights of over 1.5×103 contained 54 %, on average, of the Fe, Zn and Cu in the fulvic acid fraction, and the components with molecular weights of over 104 contained 58 %, on average, of these metals in the humic acid fraction.  相似文献   

9.
The C-13 and proton NMR spectra of marine humic and fulvic acids isolated from sediments of Sagami and Suruga Bays and Aldrich humic acid were obtained using pulse Fourier transform mode. The C-13 and proton NMR spectra, which clarified the differences in chemical characteristics among the various humic substances, showed that the marine humic acids had more aliphatic and less aromatic character than the Aldrich humic acid, and the marine fulvic acids had polysaccharide-like character. The C-13 NMR spectra of the marine humic substances, in particular, had many relatively well-resolved peaks with significant intensities, indicating the presence of variously bonded carbon atoms in them.  相似文献   

10.
Humic compounds were determined in sediments collected in an area of the Adriatic sea receiving fresh waters from the river Po. Sediment cores (10 cm) were sectioned into four layers which were analysed separately for redox potential (Eh), total phosphorus (TP), total organic carbon (TOC), humic (HA) and fulvic acid (FA) content. The structure of HA and FA was also investigated. The results showed that the TOC and TP content decreased from the coast to the open-sea stations. Humic and fulvic acid concentrations were also inversely correlated to the distance from the coast. Moreover, the humic and fulvic acids were closely correlated to the total organic content and to the total phosphorus content. The correlations found between humic substances (HS) and TOC and TP, respectively, could be explained both by an in situ formation due to the high content of nutrients and organic matter, and by a common source of HS, TOC and TP, namely the River Po discharge. The predominant presence of aliphatic carbon in the humic structures, the low degree of substitution and the high nitrogen content suggest that primarily humified compounds were formed in situ. Nevertheless, the River Po can act both as supplier of organic matter of which decomposition products lead to the formation of humic compound and as carrier of humified compounds.  相似文献   

11.
In order to improve the understanding of structural and reactive features of sediment organic matter from mangrove swamp as well as evaluate the relationship between such features and the impact from different sources (marine and terrestrial), humic and fulvic acids were isolated from two mangrove swamp sediments located in the Qinglan harbors on Hainan Island, China. One is a forest surface sediment site (WWM2), and the other is an estuary subaqueous sediment site (BMW). The humic and fulvic acids were characterized and compared using chemical and spectroscopic methods, including elemental analysis, thermogravimetric analysis (TGA), Fourier Transformed Infrared Spectroscopy (FTIR), 13C nuclear magnetic resonance (13C NMR) and potentiometric titrations. The results indicated that there were less aliphatic compounds but more aromatic compounds and oxygen-containing functional groups in fulvic acids. Humic acids contained more long-chain hydrocarbons and nitrogen compounds. Comparison of the C/N ratios and δ13C values for the humic substances at both sites indicated a larger marine and/or microbial contribution to the BMW site. Humic substances at the WWM2 site have more acidic functional groups than those of the BMW site. Compared to the literature, more phenolic groups existed in the samples of both sites, which may be due to the autochthonous contribution of mangrove plants.  相似文献   

12.
A simple method for the determination of dissolved humic acid based on carbon analysis is presented. This method was used to measure the distribution of dissolved humic acids in seven coastal plain estuaries located in the middle-Atlantic United States. Results indicate that 100% of the dissolved humic acid was removed during estuarine mixing, although concurrent measurements of dissolved organic carbon showed either production or conservative behavior in regions of the estuary where humic acid removal was observed. It is apparent from these observations that removal of dissolved humic acid is a minor part of the estuarine transport of dissolved organic carbon.Laboratory experiments carried out by mixing river water with sea water demonstrated that salt-induced removal of dissolved humic acid was insignificant in two of three estuaries studied. These results suggest in situ removal of dissolved humic acid may not be universally caused by increasing estuarine salinity.  相似文献   

13.
In seawater and lake water the complexation of several heavy metals, present in the dissolved state at relevant trace levels, with humic substances isolated from two marine and an estuarine sediment has been studied by differential pulse anodic stripping voltammetry (DPASV) at a hanging mercury drop electrode (HMDE). Taking Zn(II) as an example, the aim of this study was to gain direct information on the general level of importance of humic substances for the speciation of certain heavy metals in fresh and saline waters.In seawater humic acids originating from different sediments have very similar complexing properties for Zn(II), decreasing slightly in the order HAN > HAL > HAM. In lake water HAL is most efficient for complexing Zn(II), followed by HAN and HAM.In both types of natural waters, the sedimentary fulvic acid is less efficient in complexing Zn(II) than the respective humic acid from the same site. In general, the complexing efficiency decreases in the order EDTA > NTA > humic acids > fulvic acid.The problem of humic acid adsorption at the electrode, which somewhat limits the investigation of Pb(II) and Cd(II), and the impact of pH on the amount of complexed Zn(II) are also discussed.The findings provide further direct evidence for the conclusion previously drawn from existing complexation data that because of the rather low levels of dissolved humics in large parts of the oceans, the complexation efficiency of humics for Cd, Pb and Zn is too low to affect the speciation pattern of these three heavy metals.  相似文献   

14.
Barnacles (Balanus sp) were used to examine the uptake and release of chromium-51 added to sea water in two different valence states, 51Cr(VI) and 51Cr(III).Hexavalent chromium-51 (sodium chromate) forms a true ionic solution in filtered sea water and barnacles were able to accumulate chronium in soft tissues 543 times the levels found in sea water. The experiment showed that incorporated Cr(VI), is released to the water in such way that only 20%% of maximum uptake was lost by the organisms after 26 days. Addition of the hexavalent form to non filtered sea water showed that 2% of the total radioactivity was attached to the suspended particles. Here again chromium is mainly concentrated in soft tissues, showing a concentration factor of 380 related to total chromium available in aquarium (solution + suspended particles). From the total radioactivity incorporated by the organisms, 20 % was released after 56 days in the clearance experiment.Chromium, as trivalent chromic chloride, when added to sea water precipitates and is quickly removed from the water by the filter activity of the barnacles. Unlike the hexavalent form, trivalent chromium is not concentrated in soft tissues of the barnacles and is quickly released to the water through the organisms digestive system.  相似文献   

15.
利用元素及同位素地球化学方法研究了冲绳海槽中部沉积物岩芯中有机碳及磷的地球化学特征及影响因素。结果表明,冲绳海槽沉积速率（16.5~32.5 cm/ka）变化小,不是沉积物中有机碳埋藏的重要影响因素。相对于全新世氧化性底水环境,末次盛冰期/冰消期冲绳海槽缺氧底水环境提高了沉积物对有机碳的埋藏效率。冲绳海槽沉积物中各形态磷的相对含量与其他边缘海沉积物中的相似。交换态磷（Ex-P）含量低、变化小。末次盛冰期/冰消期缺氧底水环境下铁氧化物的还原溶解导致铁结合磷（Fe-P）释放以及自生磷矿物（Au-P）的形成。全新世氧化性底水条件有利于铁氧化物的有效再生及对磷的再吸附,但不利于Au-P的保存。总有机碳（TOC）和有机磷（Org-P）之间良好的相关性表明TOC埋藏对Org-P含量的重要控制作用。冲绳海槽沉积物中碎屑磷（De-P）含量低于长江口及东海陆架沉积物中的含量,这与陆源碎屑向外海传输减弱有关。在约9.3 ka BP（岩芯200 cm深度）,TOC、Fe-P、Org-P、De-P以及FeHR均出现的极小值可能由物质坡移造成。  相似文献   

16.
Dissolved organic matter (DOM) is comprised of a myriad of macromolecules with specific physical and chemical properties that may influence the bioavailability of hydrophobic pesticides to animals. This study was conducted to assess the role of various forms of DOM on the uptake and bioconcentration of the organophosphate insecticide chlorpyrifos (CHPY) to the bivalve Mercenaria mercenaria. Bivalves were exposed to DOM-free seawater (30 per thousand) or to seawater containing a single form of DOM. DOM forms included two filtrate fractions of natural salt-marsh sediment DOM (DOM-(<0.45 mum) and DOM-(<3 kDa)); natural purified humic (HA) and fulvic (FA) acids; and water soluble cyclic oligosaccharides alpha and beta cyclodextrins (CD-alpha and CD-beta). In (14)C-CHPY uptake and elimination experiments, juvenile bivalves were exposed to uniformly-labeled (14)C-CHPY and collected at time intervals during 48 h. The remaining bivalves were transferred to (14)C-CHPY-free elimination chambers with bivalve collection at time intervals over 144 h. Total uptake of (14)C-CHPY by bivalves in DOM-free seawater was >40% greater than in bivalves exposed to (14)C-CHPY in the presence of most DOM forms. These results are consistent with much faster (14)C-CHPY uptake rates estimated using a simple two parameter model. After the elimination period, bivalves exposed to DOM-free seawater had (14)C-CHPY body residue concentrations between 25% and 86% greater than bivalves in the presence of DOM forms. Experiments with larger bivalves showed that pulse-chase exposures with a 1.5 h exposure period to (14)C-CHPY was not long enough to detect differences in (14)C-CHPY tissue accumulation efficiencies across treatments. Our findings suggest that natural forms of DOM, at environmentally realistic organic carbon concentrations, reduced pesticide uptake and bioconcentration, consistent with much lower uptake rates relative to bivalves exposed to (14)C-CHPY in the absence of DOM. Interestingly, at the tested organic carbon concentrations CD-alpha and CD-beta did not reduce (14)C-CHPY bioconcentration in M. mercenaria.  相似文献   

17.
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   

18.
A reproducible, low-blank, isotope-dilution technique for the determination of inorganic Cr(III) and total dissolved chromium in seawater has been developed. Analysis of coastal water from Brittany, France, confirms that inorganic Cr(III) exists in excess of the thermodynamic equilibrium value calculated from the model of Elderfield (1970). A vertical profile of total chromium at 13°N on the East Pacific Rise confirms the general features of Cr behaviour: slight depletion at the surface (Cr = 2.0 nmol l−1 compared to 2.6 nmol l−1 below 1000 m) and bottom excess possibly due to Cr (III) release from sediments (up to 15.8 nmol l−1). A maximum enrichment of six times the average seawater value is obtained in hydrothermal waters. The chromium content of metalliferous sediments is mainly due to scavenging from the water column; input of chromium into the ocean through hydrothermalism is negligible.  相似文献   

19.
The interactions in seawater of cadmium, copper, and zinc with natural levels of marine humus (fulvic and humic acids) were studied using differential pulse anodic stripping voltammetry (DPASV). Interactions with Cu were also examined by ultraviolet spectrophotometry. The degree of interaction relates to the structure of the particular fulvic or humic acid tested. Marine fulvic and humic acids with different equivalent weights and varying degrees of aromaticity and heteroatom substitution were tested to assess the relative importance of these fundamental structural features in determining the degree of interaction. An index of heteroatom substitution, derived from proton magnetic resonance spectra of these materials, when combined with equivalent weights correlated with the nature and degree of metal interaction. Both marine fulvic and humic acids appreciably interacted with Zn. In contrast, the extent of interaction of fulvic acids with Cu appears to be related to their structure while humic acids appear to interact with Cu regardless of structure. Cadmium interacts only with mature, highly crosslinked humic acids.  相似文献   

20.
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   

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