The application of isotopic and biogeochemical markers to the study of the biochemistry of organic matter in a macrotidal estuary, the Loire, France   总被引：1，自引：0，他引：1  

A. Saliot  J. Tronczynski  P. Scribe  R. Letolle 《Estuarine, Coastal and Shelf Science》1988,27(6)

The biogeochemistry of organic matter in a macrotidal estuary, the Loire, France, has been studied for two years during different seasons. Both particulate matter and sediment have been sampled in the riverine zone, in the maximum turbidity zone and in the ocean near the river mouth. Two techniques have been used: carbon isotopic ratio determination and analysis of lipid-marker signatures in the n-alkane, n-alkene and fatty acid series. For the period corresponding to the output of the maximum turbidity zone in the ocean, the complete change of organic matter, continental in nature in the inner estuary, pure marine in the outer estuary is well illustrated by the decrease of δ¹³C values and of carbon preference index of n-alkanes. Input sources of organic matter by continental plants, plankton and micro-organisms are discussed from biogeochemical-marker analyses data along with the processes of accumulation of particles and their evolution with the season. Some criteria for evidencing the nature of various organic-matter pools are assessed and compared in different chemical-marker series as follows: high molecular weight n-alkanes and fatty acids, perylene for continental imprints, polyunsaturated 18-, 20- and 22-carbon fatty acids, n-C₁₇, n-alkenes and squalene for algae imprints, branched iso and anteiso fatty acids, Δ11-C_18:1 for microbial imprints.  相似文献   

Fe(OH)_3胶体与铜离子作用的研究     

张恩仁  田玉红  张正斌  刘莲生 《热带海洋学报》2001,(4)

使用切向流超滤系统得到粒度较均匀的Fe(OH)3胶体,进而对Fe(OH)3胶体粒子与Cu2 的作用进行了研究,并将实验结果与南沙群岛海区表层水中铜与胶体物质结合状况的调查数据进行了比较分析,得到如下结果:(1)在海水介质中,铜在Fe(OH)3胶体上结合的百分率(pH>5)随pH的升高而下降,随着Fe(OH)3胶体浓度的减小而下降?(2)在天然海水介质中,使铜在Fe(OH)3胶体上结合的百分率在50%-70%的有机物浓度为1.0mg·L-1,有机物浓度的增大使铜与无机胶体结合的百分率有下降的趋势?  相似文献   

Sources and hydrothermal alteration of organic matter in Quaternary sediments: A synthesis of studies from the Central Gulf of California     

Bernd R. T. Simoneit 《Marine and Petroleum Geology》1986,3(4)

Deep sea drilling in the Central Gulf of California, a young and active spreading centre, shows that the high heat flow typical of these regions causes extensive alteration of sediment organic matter, especially near sills and above magma chambers where hydrothermal activity is concentrated. Even on the nearby passive margin, where there are no sills, heat flow is moderately high and hydrocarbon generation has begun in immature sequences. Migrating light hydrocarbons are detected especially where hydrothermal activity is concentrated. Thermogenic methane is more widespread, though not in the passive margin bordering the spreading centre. Despite the incidence of hydrocarbon generation and migration, the amounts of hydrocarbons involved are relatively small and apparently do not lead to commercially significant accumulations of petroleum.The organic matter in these sediments is mostly marine because the Gulf of California generally has low runoff from land and highly productive surface waters. Turbidites rich in terrigenous organic material are locally abundant in the mainly pelagic section in the Guaymas Basin. The highest concentrations of organic matter are found in laminated diatomites deposited on the Guaymas passive margin within the oxygen minimum zone.  相似文献   

夏、冬两季长江口及邻近海域悬浮物的分布特征及其沉积量   总被引：11，自引：0，他引：11  

庞重光  王凡  白学志  张明翰 《海洋科学》2003,27(12):31-35

利用2001年7～8月 ,2002年1月两个航次的悬浮物浓度资料 ,并参考其它水文参数 ,简要分析长江口及邻近海域悬浮物的分布特征 :无论夏季还是冬季 ,长江入海悬浮物总是向东南方输运 ;冬季由于再悬浮作用显著 ,悬浮物浓度明显高于夏季 ,且南北分布范围也明显增大 ,垂向分布均匀。同时采用数值模拟的海流流速值和观测的悬浮物浓度值计算悬浮物的断面通量 ,并最终得计算区悬浮物夏、冬两季的沉积量 ,夏、冬季长江口及邻近海域悬浮物的沉积量分别为0.79×108t,1.44×108t。  相似文献   

悬浮沙激光散斑图像处理的研究     

杜军兰  陈靖齐  于连生  刘海坤  徐雷 《海洋技术学报》2001,20(1):107-111

本文以统计模式识别为基础，阐述了图像处理在悬浮沙粒粒径流量中的实际应用，提出了用图像层析来确定放大系数的方法，提出了测量的准确度。  相似文献   

Quantum yield for the photochemical production of dissolved inorganic carbon in seawater   总被引：2，自引：0，他引：2  

Sophia C. Johannessen  William L. Miller 《Marine Chemistry》2001,76(4):108

The direct photooxidation of coloured dissolved organic matter (CDOM) to dissolved inorganic carbon (DIC) may provide a significant sink for organic carbon in the ocean. To calculate the rate of this reaction on a global scale, it is essential to know its quantum yield, or photochemical efficiency. We have determined quantum yield spectra, φ(λ), (moles DIC/mole photons absorbed) for 14 samples of seawater from environments ranging from a turbid, eutrophic bay to the Gulf Stream. The spectra vary among locations, but can be represented quite well by three pooled spectra for zones defined by location and salinity: inshore φ(λ)=e^{−(6.66+0.0285(λ−290))}; coastal φ(λ)=e^{−(6.36+0.0140(λ−290))}; and open ocean φ(λ)=e^{−(5.53+0.00914(λ−290))}. Production efficiency increases offshore, which suggests that the most highly absorbing and quickly faded terrestrial chromophores are not those directly responsible for DIC photoproduction.  相似文献   

Distributions of dissolved and particulate biogenic thiols in the subartic Pacific Ocean     

Christopher L. Dupont  James. W. Moffett  Robert R. Bidigare  Beth A. Ahner 《Deep Sea Research Part I: Oceanographic Research Papers》2006,53(12):1961-1974

Dissolved and particulate concentrations of the biogenic thiols cysteine (Cys), arginine–cysteine (Arg–Cys), glutamine–cysteine (Gln–Cys), γ-glutamate–cysteine (γ-Glu–Cys) and glutathione (GSH) were measured in the subartic Pacific Ocean in the summer of 2003 using high performance liquid chromatography (HPLC) with precolumn derivatization as reported in previous work. In this study, a preconcentration protocol for the derivatized thiols was utilized to extend detection limits of dissolved thiols to picomolar levels. The measured concentrations of particulate and dissolved thiols were uncoupled, with distinctive depth profiles and large differences in the particulate to dissolved ratios between individual compounds. Glutathione was the most abundant particulate thiol whereas the most abundant dissolved thiol was γ-Glu–Cys, with concentrations as high as 15 nM. Given the relatively small pool of intracellular γ-Glu–Cys and the very low dissolved concentrations of GSH, we hypothesize that glutathione released from cells is rapidly converted to the potentially degradation resistant γ-Glu–Cys outside the cell. The relatively high concentrations of other dissolved thiols compared to particulate concentrations implies both biological exudation and slow degradation rates. Some thiols appear to vary with changes in nutrient availability but this effect is difficult to decouple from changes in community structure inferred from pigment analyses. Dissolved thiol concentrations also exceed typical metal concentrations in the subartic Pacific, supporting previous arguments that they may be important in metal speciation.  相似文献   

东海海域海水中颗粒氨基酸(PAA)的组成与含量的分布调查研究     

李烈英  张星君  纪明侯 《海洋科学集刊》2004,46(46):100-105

海水中的有机物的含量微少，约为0.5~2.0 C mg/L，但其种类复杂。其中以溶解有机物(DOM)为主，而颗粒有机物(POM)所占比例则更少。大洋海水中的POM主要来源于浮游生物等的死骸及其分解碎屑；另外还有海水中受风浪影响所进行的DOM-POM的动力平衡产物。近岸海水还受河流和大气带入的陆源尘影响。POM主要由颗粒氨基酸(PAA)组成。即由Asp、Glu、Thr、Ser、Ala、Gly、Leu、Ile、Val、Met、Cys、Tyr、Lys、His、Arg、Phe、Pro等17种氨基酸组成。它们是食碎动物的主要食物，构成海洋食物链的一环，与该水域生产力有直接联系。纪明侯等(1992)于1983年和1984年首次对青岛胶州湾海水中的颗粒氨基酸的组成和含量的变化及其季节变化进行了调查研究。并且在1982年和1984年前后对渤海湾、黄河口和长江口附近水域同样调查研究了表层海水中PAA的组成与含量分布。他们还于1981年7、8月和1982年7、8月乘“科学一号”考察船进一步研究了长江口外东中国海，包括福建省外海、济州岛附近海域和黑潮流域26°00′-33°00′N、123°00′-129°00′E范围内海域的20余个站位的表层海水和部分站位上不同水深中的PAA的组成和含量。兹将调查研究结果报道如下。  相似文献   

悬对沙Mellor-Yamada海洋边界层模型计算结果的影响     

李华军  梁丙臣  李东永  李磊岩 《海洋科学》2004,28(1):27-32

为了分析海洋水体垂向水流紊动及紊动交换情况而采用了一维的海洋边界层模型(Mellor-Yamada)并利用数值实验的方法对悬沙、盐度、温度等数据进行分析。原模型未将悬沙考虑在内，本文试将它引入进去探讨由于它的存在对紊动混合特性的影响。2000年4月，Mellor将最初的模型引入了依赖于Richardson数的紊动动能耗散率。本文通过比较具有悬沙和不具有悬沙两种情况下的速度、温度和盐度垂向分布随时间的变化，分析讨论由于悬沙的存在所引发的密度层化对紊动混合作用的影响，并发现悬浮泥沙抑制了部分模拟时间的紊动混合作用。  相似文献   

Complexation of mercury by dissolved organic matter in surface waters of Galveston Bay, Texas   总被引：3，自引：0，他引：3  

Seunghee Han  Gary A. Gill  Ronald D. Lehman  Key-Young Choe 《Marine Chemistry》2006,98(2-4):156-166

The chemical speciation of dissolved mercury in surface waters of Galveston Bay was determined using the concentrations of mercury-complexing ligands and conditional stability constants of mercury-ligand complexes. Two classes of natural ligands associated with dissolved organic matter were determined by a competitive ligand exchange-solvent solvent extraction (CLE-SSE) method: a strong class (L_s), ranging from 19 to 93 pM with an average conditional stability constant (K_HgLs) of 10²⁸, and a weak class (L_w) ranging from 1.4 to 9.8 nM with an average K_HgLs of 10²³. The range of conditional stability constants between mercury and natural ligands suggested that sulfides and thiolates are important binding sites for dissolved mercury in estuarine waters. A positive correlation between the estuarine distribution of dissolved glutathione and that of mercury-complexing ligands supported this suggestion. Thermodynamic equilibrium modeling using stability constants for HgL, HgCl_x, Hg(OH)_x, and HgCl(OH) and concentrations of each ligand demonstrated that almost all of the dissolved mercury (> 99%) in Galveston Bay was complexed by natural ligands associated with dissolved organic matter. The importance of low concentrations of high-affinity ligands that may originate in the biological system (i.e., glutathione and phytochelatin) suggests that the greater portion of bulk dissolved organic matter may not be important for mercury complexation in estuarine surface waters.  相似文献