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1.
高邮湖、南四湖和东平湖作为南水北调东线枢纽湖泊,其水质状况对保障调水安全起到关键性作用本文运用三维荧光光谱平行因子分析法(EEMs-PARAFAC)分析了3个湖泊在不同水文情景下有色可溶性有机物(CDOM)吸收、荧光光谱特征以及荧光组分与主要水质参数的相关性,以探究3个湖泊CDOM来源组成特征结果表明,平行因子分析法解析CDOM三维荧光图谱,得到陆源类腐殖质C1、类色氨酸C2和类酪氨酸C3不同水文情景对高邮湖CDOM来源与结构组成影响较明显,丰水期其类腐殖质荧光强度显著大于枯水期(t-test,P0.01),并且与a(254)呈正相关(R~2=0.85,P0.01),表明类腐殖质是CDOM主要部分,该荧光组分贡献率可达50%[F_(max)C1/(F_(max)C1+F_(max)C2+F_(max)C3)×100%],高邮湖受到入湖河流来水的影响较大,丰水期入湖口附近荧光强度明显高于其他水域东平湖和南四湖CDOM来源组成特征相似,丰水期东平湖和南四湖组分C2和C3显著低于枯水期(t-test,P0.01),两湖泊枯水期工农业等人为污染源影响较大相关性分析表明高邮湖中类腐殖质荧光特征在一定程度是能反演DOC浓度,并且类腐殖质的输入会增加湖泊总磷、总氮和叶绿素a浓度而东平湖和南四湖CDOM荧光特征与主要水质参数的相关性较差,这与高邮湖水体存在较大差异. 相似文献
2.
Loreto Rossi M. Letizia Costantini Pasquale Carlino Antonella di Lascio David Rossi 《Aquatic Sciences - Research Across Boundaries》2010,72(2):227-236
The high numbers of primary producers represent multiple sources of organic matter accumulating onto lake bottoms. The difficulty
of distinguishing the relative contribution to the mixture presents considerable challenges to the analysis of these organic
deposits. In this study, dual-stable isotope analysis and IsoSource model were used to identify allochthonous and autochthonous
components of detritus deposits (Particulate Organic Matter: POM) at two different bottom slope sites of a volcanic lake (lake
Bracciano). Experiments were carried out to calibrate IsoSource on constructed plant mixtures and assess changes in isotope
ratios during plant decomposition. IsoSource satisfactorily discriminated the constructed mixture sources with a few exceptions.
Changes in isotopic enrichment during decomposition were low, and thus did not represent a confounding variable in the isotopic
analysis. By contrast, chemical and geological differences of the study sites were associated with differences in plant δ13C and δ15N values (more than 2‰ within single plant species). At both sites, the isotopic signals of POM fell between polygons delineated
by source end members with an evident shift of δ13C toward allochthonous sources. POM amount and diversity were greater at the flatter bottom site, where allochthonous contributions
were larger than at the other site. In particular, IsoSource ranked species contributions as follows: A. glutinosa > P. australis > A. donax > S. alba > P. nigra > the benthic macroalga Chara sp. at the first site, and A. glutinosa > P. nigra > the aquatic macrophyte C. demersum at the latter. The composition of littoral POM was determined by allochthonous sources in proportion to their relative abundances
(as percent land cover) with differences between sites due to bottom slope. 相似文献
3.
长三角地区大部分湖泊为非通江湖泊,地势低平,港汊及闸坝众多,水流宣泄不畅,水力滞留时间较长,加之周边地区城镇人口稠密.因此与水滞留时间短的通江湖泊相比,非通江湖泊的有色可溶性有机物(CDOM)来源和组成具有差异性.本文选取了3个重要的中型非通江供水湖泊——滆湖、淀山湖和阳澄湖,对枯水期、平水期、丰水期3种水文情景下CDOM组成结构变化特征进行分析,从而进一步揭示该类湖泊CDOM来源和对水文情景响应的内在机理.结果表明:滆湖、淀山湖和阳澄湖通过平行因子分析法得到2种类腐殖质(C1和C4)和2种类蛋白质(C2和C3),湖泊CDOM结构受到降雨事件和人类活动的双重影响.三个湖泊类蛋白质的高值在空间上主要集中在人类活动频繁的湖区,并且类蛋白质平均荧光强度与叶绿素a浓度相关性较差,说明湖泊类蛋白质组分受到内源藻类降解、外源人类生产生活排放双重作用的影响.三个湖泊类蛋白质的平均荧光强度和总氮浓度均在枯水期显著高于丰水期,说明降雨量的增加可以稀释湖泊有机质浓度;同时,陆源类腐殖质C1与溶解性有机碳、总氮、总磷、叶绿素a浓度呈显著正相关,并且随着降雨量增加,类蛋白质的占比逐渐降低,滆湖从86.84%降低至62.49%,淀山湖从96.53%降低至90.56%,阳澄湖从98.40%降低至96.26%,说明降雨事件也可以增强径流的冲刷作用,携带更多腐殖化程度高的陆源有机质进入湖泊.本研究发现降雨过程和人类活动共同作用于滆湖、淀山湖和阳澄湖CDOM库,研究结果可以为进一步保障太湖流域人类用水安全提供参考依据. 相似文献
4.
Parallel factor analysis of fluorescence excitation emission matrices of surface water samples of a globally large river (Yangtze River, China) watershed identified three classes of fluorescent dissolved organic matter (FDOM) that had ex/em = 280/330 nm, 305/385 nm and 350/450 nm respectively, resembling “peak T”, “peak M” and “peak C” commonly identified in natural water, respectively. Peak T (a tyrosine/tryptophan-like FDOM) did not show correlations to peak M or C which were humic-like substances, while a positive correlation (r = 0.935, p < 0.001) was present between the natural log-transformed maximum fluorescence intensity (Fmax) of peaks T and M indicating a tight link during their production and processing. Fmax values (in Raman unit nm?1) normalized to dissolved organic carbon (DOC) concentration were low, varying in ranges 15.93–85.95, 29.83–83.54 and 19.73–51.05 × 10?5 nm?1 (μmol/L)?1 for peaks T, M and C, respectively, in line with the history of strong photobleaching of the water samples as indicated by fairly high absorption spectral slope ratios (0.75–1.53 with a mean 1.03). Intermediate fluorescence index (FI) (1.46–1.83 with a mean 1.61) and small specific absorption at 254 nm (0.64–1.93 with a mean 1.15 m?1 mg?1 L) of the water samples, indicated the presence of both aquatic microbial DOM (e.g. peak T) and soil DOM (e.g. peak C). Peak C could be substantially removed by UV-A (320–400 nm) irradiation, while peak M was slightly increased when a microbe-containing water was exposed to the same UV-A irradiation. Taken together, peak C was attributed to diffuse soil source while peak M was likely attributed to joint effects of microbial activities and solar irradiation on the chromophores in the sample. 相似文献
5.
The degradation behaviour of a phenolic waste-water from coking containing easily utilizable carbon sources (volatile fatty acids), substances with toxic effects (phenols and phenolic compounds), and non-biodegradable organic substances (humic-like substances) by an adapted activated sludge is investigated depending on dissolved oxygen concentration (DO) and temperature. In addition, the degradation of an acetate model water with the same population was investigated. The investigations were carried out in a special respiration fermenter system by recording oxygen consumption in DO-static experiments. The oxygen consumption curves were subjected to linear regression analysis, and the maximum oxygen consumption rates were used for further calculations. Evaluation of the degradation kinetics was carried out with non-linear regression analysis via commercial software utilizing the Marquardt-Levenberg algorithm and which tested various kinetic models to obtain the best curve fit. It is shown that the dependence of growth on DO in acetate model water is well represented by Monod kinetics but by contrast can only be described in phenolic wastewater with acceptable goodness by Hill kinetics, modified by a maintenance term. The kinetic constants calculated for the mesophilic range (37 °C) are for the model water as follows: maximum specific growth rate = 0.218 h?1, half saturation constant with respect to oxygen = 0.297 g L?1, and for the waste-water: maximum specific growth rate = 0.387 h?1, half saturation constant with respect to oxygen = 0.013 gL?1 and maintenance coefficient for oxygen = 0.107 g g?1 h?1. For the thermophilic range (55 °C), a higher growth rate but a significant lower yield coefficient are to be observed. The kinetic constants calculated are: maximum specific growth rate = 0.8 h?1, half saturation constant with respect to oxygen = 0.14 gL?1 and maintenance coefficient for oxygen = 0.3 g g?1 h?1. Therefore, it can be concluded that the toxic effect of the biodegradable phenols causes a maintenance metabolism which leads to higher oxygen demand. The diminution of the limiting DO and the increased maintenance metabolism confirm the assumption that a higher maintenance metabolism leads to increased sensitivity with respect to the cosubstrate oxygen. It can be concluded that the experimental and mathematical methods used permit the maintenance metabolism with respect to oxygen caused by toxic substrates and milieu influences to be accurately determined. 相似文献
6.
为探究富营养化湖泊中自生源可溶有机质(DOM)在泥水界面的吸附行为,以马来眼子菜(Potamogeton malaianus)和铜绿微囊藻(Microcystis aeruginosa)释放的DOM为代表,考察针铁矿对草、藻源DOM中不同组分的吸附特征.三维荧光平行因子分析表明类富里酸组分C1和类胡敏酸组分C4的含量很低,而类蛋白物质(类酪氨酸组分C2和类色氨酸组分C3)分别占草、藻源DOM荧光组成的70%和93%. 2种DOM均可被针铁矿吸附,吸附过程符合伪一级动力学.通过等温线拟合发现针铁矿吸附藻源DOM的非线性更强,饱和吸附量(23.77 mg/g)高于草源DOM(19.10 mg/g).特别地,类蛋白组分呈现非线性吸附,而类腐殖物质的吸附近似线性,且针铁矿对于DOM各荧光组分的吸附量顺序为:C3C2 C4 C1,此非均质吸附特征与DOM组分的初始含量、分子大小、芳香性及有效吸附位点有关.红外光谱证实氨基、羧基和羟基是吸附过程中的重要官能团.因此,草、藻源DOM显著改变了针铁矿表面的有机物质组成,影响湖泊沉积物的生物地球化学行为. 相似文献
7.
化学需氧量(COD)、五日生化需氧量(BOD_5)及溶解性有机碳(DOC)是指示湖泊水质的重要指标,然而上述指标测定通常耗费大量时间、试剂及人力物力且排放大量有害废液.有色可溶性有机物(CDOM)是溶解性有机物(DOM)中可以强烈吸收光谱中的紫外光和可见光的部分,数据测定耗时短、方便快捷,且样品处理过程环境友好,能在很大程度上反映湖泊水质.本研究基于2016年2、5和8月在太湖均匀布设的32个采样点进行样品采集,运用光谱吸收与三维荧光-平行因子分析(EEMs-PARAFAC)探究太湖CDOM的光谱吸收和荧光组分,探讨CDOM光谱指标对湖泊BOD_5、COD及DOC浓度等湖泊环境质量指标的可替代性.结果表明:(1)运用EEMs-PARAFAC方法解析出3种荧光组分:类腐殖酸C1、类酪氨酸C2和类色氨酸C3.(2) COD和BOD_5和DOC在空间上呈现出相似的分布趋势,不同水期的最高值均出现在竺山湾和梅梁湾,由西北湖区至中部敞水区、东南湖湾递减.(3)在不同水期,COD、BOD_5、DOC浓度和C1组分均表现为丰水期极显著大于枯水期和平水期,a_(254)在丰、平、枯水期间无显著性差异,最大值出现在丰水期;C2与C3组分均在枯水期和平水期极显著大于丰水期.(4)在不同水文时期,COD、BOD_5和DOC浓度均与a_(254)、类腐殖酸C1呈显著正相关,丰水期太湖COD、BOD_5和DOC浓度与CDOM光谱指标的线性相关性要优于枯水期和平水期.(5) CDOM光谱指标在不同水文时期均能很好地替代COD、BOD_5和DOC等作为反映太湖水体中有机物污染程度及湖泊水质的指标. 相似文献
8.
Sonia Regina Giancoli Barreto Wagner José Barreto Elisangela Manjurma Deduch 《洁净——土壤、空气、水》2011,39(4):362-367
The values for the partition coefficient (Kd) were calculated for Ca, Mg, Cd, Cr, Cu, Fe, Mn, Pb, Ni, and Zn at 19 sites in the Capivara hydroelectric reservoir in Brazil. It was found that the relative values of Kd follow the order: Cr > Mn > Fe > Cu > Zn > Ni > Pb > Ca > Cd, differing from the values reported for Kd in aquatic systems in the northern hemisphere. A hierarchical cluster analysis and linear correlations showed that Cr is strongly associated with Fe and Cu, and that Cd is the only metal found in complexation with organic matter, explaining its higher solubility. 相似文献
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10.
Sixteen samples of fulvic acids and XAD‐4 fractions of riverine, estuarine, coastal, and open ocean origin have been studied by emission and synchronous molecular fluorescence spectroscopy. Certain features of the molecular fluorescence are related to the nature, the content, and the origin of those aquatic humic substances (HS). Riverine HS appear several times richer in fluorophores than marine HS, which can be well observed by emission fluorescence spectroscopy. Synchronous‐scan spectra of fulvic acids and of XAD‐4 fractions from the aquatic environments studied, emphasized the quality differences of their fluorophores. These features are useful as tracers of humic substances related with their natural environment source or even with their anthropogenic origin. 相似文献
11.
The Xushen gas field, located in the north of Songliao Basin, is a potential giant gas area for China in the future. Its proved reserves have exceeded 1000×108 m3 by the end of 2005. But, the origin of natural gases from the deep strata is still in debating. Epimetamorphic rocks as a potential gas source are widely spreading in the northern basement of Songliao Basin. According to pyrolysis experiments for these rocks in the semi-confined system, gas production and geochemistry of alkane gases are discussed in this paper. The Carboniferous-Permian epimetamorphic rocks were heated from 300°C to 550°C, with temperature interval of 50°C. The gas production was quantified and measured for chemical and carbon isotopic compositions. Results show that δ 13C1 is less than −20‰, carbon isotope trend of alkane gas is δ 13C1<δ 13C2<δ 13C3 or δ 13C1<δ 13C2>δ 13C3, these features suggest that the gas would be coal-type gas at high-over maturity, not be inorganic gas with reversal trend of gaseous alkanes (δ 13C1>δ 13C2>δ 13C3). These characteristics of carbon isotopes are similar with the natural gas from the basin basement, but disagree with gas from the Xingcheng reservoir. Thus, the mixing gases from the pyrolysis gas with coal-typed gases at high-over maturity or oil-typed gases do not cause the reversal trend of carbon isotopes. The gas generation intensity for epimetamorphic rocks is 3.0×108–23.8×108 m3/km2, corresponding to R o from 2.0% to 3.5% for organic matter.
相似文献12.
Natural gases discovered up to now in Lishui Sag, the East China Sea Basin, differ greatly in gaseous compositions, of which hydrocarbon gases amount to 2%–94% while non-hydrocarbon gases are dominated by CO2. Their hydrocarbon gases, without exception, contain less than 90% of methane and over 10% of C2 + heavier hydrocarbons, indicating a wet gas. Carbon isotopic analyses on these hydrocarbon gases showed that δ 13C1, δ 13C2 and δ 13C3 are basically lighter than −44‰, −29‰ and −26‰, respectively. The difference in carbon isotopic values between methane and ethane is great, suggesting a biogenic oil-type gas produced by the mixed organic matter at peak generation. δ 13 \( C_{CO_2 } \) values of nonhydrocarbon gases are all heavier than −10‰, indicating a typical abiogenic gas. The simulation experiment on hydrocarbon generation of organic matter in a closed gold-tube system showed that the proportion of methane in natural gases produced by terrigenous organic matter in the Lingfeng Formation marine deposit is obviously higher than that in natural gases derived from the aquatic and terrigenous mixed organic matter in the Yueguifeng Formation lacustrine deposit, consequently the proportion of heavier hydrocarbons of the former is remarkably lower than that of the latter. Moreover, δ 13C1 values of natural gases produced by terrigenous organic matter in the Lingfeng Formation marine deposit are about 5‰ heavier than those of natural gases derived from the aquatic and terrigenous mixed organic matter in the Yueguifeng Formation lacustrine deposit while δ 13C2 and δ 13C3 values of the former are over 9‰ heavier than those of the latter. Currently the LS36-1 oil-gas pool is the only commercial oil-gas reservoir in Lishui Sag, where carbon isotopic compositions of various hydrocarbon components differ greatly from those of natural gases produced by the Lingfeng Formation organic matter but are very similar to those of natural gases derived from the Yueguifeng Formation organic matter, therefore, natural gases in the LS36-1 oil-gas pool are mainly derived from the Yueguifeng Formation lacustrine source rock rather than the Lingfeng Formation marine or Mingyuefeng Formation coal-measures source rocks.
相似文献13.
Nutrient fluxes across terrestrial-aquatic boundaries and their subsequent integration into lake nutrient cycles are currently
a major topic of aquatic research. Although pollen represents a good substrate for microorganisms, it has been neglected as
a terrestrial source of organic matter in lakes. In laboratory experiments, we incubated pollen grains of Pinus sylvestris in water of lakes with different trophy and pH to estimate effects of pollen input and its subsequent microbial degradation
on nutrient dynamics. In this ex situ experiment, we measured concentrations of organic carbon, phosphorus and nitrogen in the surrounding water as well as microbial
dynamics (bacteria and fungal sporangia) at well-controlled conditions. Besides leaching, chemical and microbial decomposition
of pollen was strongest within the first week of incubation. This led to a marked increase of soluble reactive phosphorus
and total dissolved nitrogen (up to 0.04 and 1.5 mg L−1, respectively, after 5 days of incubation) in the ambient water. In parallel, pollen grains were rapidly colonized by heterotrophic
bacteria and aquatic fungi. Leaching and microbial degradation of pollen accounted for ≥80, ≥40, ≥50% for organic C, N and
P, respectively, and did not significantly differ among water samples from the studied lakes. Thus, pollen introduces high
amounts of bio-available terrestrial organic matter and nutrients into surface waters within a short time. A rough calculation
on P input into oligotrophic Lake Stechlin indicates that pollen plays an important ecological role in nutrient cycling of
temperate lakes. This requires further attention in aquatic ecology. 相似文献
14.
湖泊生态系统作为自然界重要的碳库,光照强度的变化对于湖泊的碳循环过程可能产生重要的影响.以云南老君山高山湖泊天才湖周边土壤中的腐殖酸作为外源溶解性有机物（DOM）的代表物,通过腐殖酸模拟光降解实验,考察光照强度对外源DOM光降解过程的影响.研究结果表明：腐殖酸光吸收系数a440、465 nm和665 nm波长处吸光度比值E4/E6的下降幅度均为：对照组 < 20 W光照组 < 40 W光照组,a440、E4/E6和光谱斜率SR显著相关,表明紫外辐射使得腐殖酸溶液浓度降低、相对分子量下降,且光照强度越强,腐殖酸的光降解程度越大.通过EEM-PARAFAC模型识别出光降解过程中腐殖酸溶液中含有5种荧光组分：UV类腐殖质（C1）、UVA类腐殖质（C2）、类色氨酸（C3）、UVC类腐殖质（C4）和类络氨酸（C5）.40 W光照组中4种荧光组分的降解程度与降解速率均大于20 W光照组,降解程度均为：C4 > C3 > C2 > C1,降解速率为C2 > C4 > C3 > C1,说明不同的荧光组分对光照强度的响应不同.该研究有助于阐明外源DOM的光降解途径与归趋. 相似文献
15.
基于2017年1-12月在抚仙湖开展的逐月观测,利用紫外-可见吸收光谱和三维荧光光谱技术探讨该湖有色可溶性有机物（CDOM）的来源组成及时空变化特征.12个月CDOM吸收值a（254）的均值为3.47±0.57 m-1,范围为1.82~5.22 m-1,说明CDOM丰度较低.平行因子分析结果给出了2种类酪氨酸荧光组分（C1和C3）、1种类色氨酸荧光组分（C2）、1种类腐殖质荧光组分（C4）,12个月内源组分（C1+C3）对总荧光强度的平均贡献为65.81%±15.38%,外源组分（C2+C4）的平均贡献为34.19%±15.38%;荧光指数FI的均值为1.73±0.14,腐殖化指数HIX的均值为1.02±0.37,生源化指数BIX的均值为1.23±0.27,说明CDOM主要为微生物内源产生.时空变化方面,春（3-5月）、夏（6-8月）、秋（9-11月）和冬（1、2、12月）季的a（254）分别为3.20±0.47、3.76±0.64、3.67±0.50和3.23±0.38 m-1,夏季和秋季均显著高于冬季和春季;CDOM丰度及内外源组分的空间分布具有季节异质性,可能与流域土地利用、河流输入、降雨、温度、光辐射等因素有关. 相似文献
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周村水库汛期暴雨中溶解有机物(DOM)的光谱特征及来源解析 总被引：2，自引：2，他引：0
运用三维荧光光谱（EEMs）技术结合平行因子分析法（PARAFAC）,对周村水库夏季两场暴雨不同降雨历时以及分子量的溶解有机物光谱特征和来源进行分析.结果表明：周村水库不同暴雨荧光光谱中出现了5种组分,分别为类腐殖质（C1、C2）、可见区富里酸（C3）和类蛋白（C4、C5）;相关性分析显示C1与C2、C3、C4以及C5具有显著的相关性,C2与C3具有显著的相关性,C3与C4以及C5具有显著的相关性;同一分子量下的雨水有机质总荧光强度以及各组分荧光强度随着降雨历时的增加均呈下降趋势,并且在各个历时和分子量间差异明显;同一降雨历时下,第一场暴雨总荧光强度随着分子量的减少而增加,第二场暴雨总荧光强度随着分子量的减少而减少;两场暴雨都呈现自生源的特征,其中第一场暴雨具有以陆源输入为主的特征;组分C1和C3与水质参数硝态氮、氨氮、总氮以及有机碳呈显著相关性.通过对暴雨在不同降雨历时以及分子量DOM光谱特征研究,可以进一步分析水库外源输入的天然有机质特征,为水库水质管理提供技术支持. 相似文献
18.
Recycling the large amounts of organic wastes produced by agriculture, forestry, urban and industrial activities as soil, organic amendments are the most popular and efficient option for avoiding their dispersion in the environment and restoring, maintaining, and/or improving the content of soil organic matter. Chemical stability and biological maturity are two important factors for the successful use of organic wastes in agriculture with limited risk for the surrounding environment. Stabilization and maturation of raw organic wastes inherently imply the achievement of an extensive humification, that is, a wide conversion of easily degradable organic matter to refractory organic compounds that resemble native soil humic substances (HS). Soil HS are the most important components of soil organic matter responsible of several soil functions and processes. As a consequence, the amount and quality of HS‐like fractions in any organic amendment are believed to be of primary importance for its agronomic efficacy, environmental safety and economic value. The first part of this review focuses on the chemical and physico‐chemical changes occurring in the humic substances (HS) ‐like fractions of organic wastes of various nature and sources subjected to common treatment processes aimed at producing environmentally‐safe soil amendments with beneficial agronomic properties. The second part discusses the composition, structure, and chemical reactivity of the HS‐like components in organic amendments of various origins and nature, and their effects on native soil HS. The review concludes by highlighting the need for innovative research targeted mainly to achieve a better fundamental understanding of the molecular structure and reactivity of soil HS and HS‐like fractions in organic amendments, the mechanisms of HS formation and transformations in the natural environment and during the treatment processes of raw organic wastes, the interactions with metals and organic xenobiotics, and the direct physiological effects that HS may exert on plants. 相似文献
19.
Distribution and significance of C~_(40) alkanes in the extracts of Cretaceous source rocks from the Songliao Basin 总被引：2，自引：0，他引：2
Feng ZiHui Fang Wei Zhang JuHe Li ZhenGuang Huang ChunYan Wang Xue Zhao QinLing Huo QiuLi 《中国科学D辑(英文版)》2007,50(10):1510-1520
Source rock extracts and crude oils from the Songliao Basin were analyzed by high-temperature gas chromatography (HTGC), gas chromatography-mass spectrometry (HTGC-MS) and gas chromatography-isotope ratio-mass spectrometry (GC-IRMS), for high molecular-weight alkanes. The distributions of n-alkanes in the Nenjiang Formation extracts are in the C14―C63 range; a bimodal distribution occurs in the C-21 and C21―40 regions. The C30―C37 n-alkanes are accompanied by C29―C35 hopanes, whereas the high molecular-weight C45―C47 n-alkanes co-occur with abundant isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The high δ 13C values of the n-alkanes and the microscopic maceral compositions indicate a highly diversified organic source input for the Nenjiang Formation source rocks, ranging from aquatic plants, blue alge-bacteria, to land plant material. In contrast, n-alkanes in the rock extracts of the Qingshankou Formation are characterized by a single modal distribution, with relatively low abundances of C29―C35 hopanes, but high molecular-weight isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The relatively low δ 13C values of C22―C44 n-alkanes and organic material compositions indicate that the source rocks in the Qingshankou Formation contain dominantly type I algal organic matter. The relative abundance of C 40 compounds in source rocks changes little at low maturity stage, but decreases drastically at higher maturity levels, with a concurrent reduction in the odd/even carbon predominance. In crude oils, in contrast, the relative abundance of C 40 compounds appears to relate closely with the oil source and oil viscosity. 相似文献
20.
《Marine pollution bulletin》2014,83(1-2):155-166
Recently compiled databases facilitated estimation of basin-wide benthic organic biomass and turnover in the Strait of Georgia, an inland sea off western Canada. Basin-wide organic biomass was estimated at 43.1 × 106 kg C and production was 54.6 × 106 kg C yr−1, resulting in organic biomass turnover (P/B) of 1.27 × yr−1. Organic biomass and production for sub-regions were predictable from modified organic flux (r2 > 0.9). P/B declined significantly with increasing modified organic flux, suggesting greater biomass storage in high flux sediments. Biomass and production were highest, and P/B lowest near the Fraser River. Annual basin-wide benthic production was 60% of previously estimated oxidized organic flux to substrates, which agrees with proportional measurements from a recent, localized study.Deviations from expected patterns related to organic enrichment and other stressors are discussed, as are potential impacts to benthic biomass and production, of declining bottom oxygen, increasing bottom temperature and potential changes in riverine input. 相似文献