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1.
双台子河口水体有机碳分布特征研究 总被引：1，自引：0，他引：1
于2011年5月和8月通过研究双台子河口水体溶解有机碳(DOC)、颗粒有机碳(POC)和化学耗氧量(COD)的分布特征,阐述双台子河口水体有机碳的河口过程及其影响因素,并探讨总有机碳(TOC)和COD表征河口有机污染的区域性和季节性特征。研究表明:2011年5月双台子河口DOC、POC和COD含量范围分别为4.04~5.06mg/L(平均4.60mg/L)、2.93~10.85mg/L(平均7.01mg/L)和5.65~14.07mg/L(平均9.04mg/L);8月分别为10.87~46.04mg/L(平均26.75mg/L)、0.88~17.27mg/L(平均4.16mg/L)和2.42~67.62mg/L(平均17.85mg/L)。DOC、POC和COD的含量由河到海总体呈现逐渐降低的趋势,双台子河口不同区段DOC、POC和COD的时空分布,及其主要和次要影响因素具有一定的差别。有机碳来源和海水的稀释作用是影响双台子河口有机碳分布的主要因素,现场生物生产和悬浮颗粒物影响较小。双台子河口水体中TOC和COD呈现线性不显著正相关关系,二者关系的季节差异显著。 相似文献
2.
基于水淘选分级的长江口最大浑浊带附近颗粒有机碳的来源、分布和保存 总被引：6，自引：6，他引：0
从分粒级的角度研究大河河口颗粒有机碳的输送特征是深刻理解河口淡咸水混合过程中有机碳的生物地球化学过程的关键。于2011年6月采集了长江口最大浑浊带附近盐度梯度下的表层悬浮颗粒物,采用水淘选方法对其按照水动力直径大小进行了分级分离,分析了这些颗粒物的有机碳含量、稳定碳同位素组成及颗粒物比表面积等参数,讨论了不同粒级颗粒物上有机碳的来源、分布和保存随盐度的变化特点及其影响因素。结果表明,随着盐度的增加和粒径的增大,长江口最大浑浊带附近分级颗粒有机碳逐渐降低,颗粒有机碳含量主要集中在小于32μm的粒级。相对于长江干流,长江口颗粒有机碳含量偏低,可能归因于河口最大浑浊带附近特殊的生物地球化学作用,如细颗粒物絮凝——沉降、微生物分解等。基于蒙特卡洛模拟的三端元混合模型的计算表明长江口分级颗粒有机碳主要来源于河流和三角洲输入,海洋来源贡献较小,三者的平均贡献比例分别为40%、35%和25%。在河口盐度梯度的淡水端,不同粒级颗粒物上三角洲来源的有机碳比例均随着盐度升高而增加,而在咸水端,海源有机碳的贡献比例升高,尤其是在16-32μm粒级,最高达39%。32-63μm粒级的颗粒物单位比表面积有机碳含量均大于1.0mg/m~2,小于32μm的颗粒物单位比表面积有机碳含量均在0.4-1.0mg/m~2的范围之内,符合河流颗粒物的一般特点,同时也说明细颗粒物上的有机碳可能已经发生了一定程度的分解,不过相对于长江口表层沉积物,颗粒物单位比表面积有机碳含量普遍较高,表明这些颗粒有机碳在沉降过程中或沉积之后还要经历进一步的再矿化分解,初步的估算表明,长江所输送的陆源有机碳约71%会在沉积过程中损失掉。本研究有助于深入了解大河河口不同粒级颗粒物在有机碳迁移转化过程中的作用,深化对高浊度河口有机碳生物地球化学过程的认识。 相似文献
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大河影响下的边缘海沉积有机碳输运与埋藏及再矿化研究进展 总被引：4，自引：0，他引：4
大河影响下的边缘海是陆源输入物质的主要储库,也是有机碳埋藏和再矿化的主要场所,在全球碳的生物地球化学循环中有着重要作用。从有机碳的输运、埋藏和再矿化等方面综述了大河影响下的边缘海沉积有机碳生物地球化学研究的最新进展。研究表明,有机碳的来源、组成、粒径和密度分布等显著影响着有机碳的分布特征和归宿,大河影响下的边缘海中移动泥等特殊沉积环境在有机碳的输运、埋藏和再矿化分解等方面发挥了独特的作用;微生物分解作用则是边缘海沉积有机碳,特别是难降解陆源有机碳发生分解的重要因素。综合运用分子生物学、有机地球化学、生物地球化学等多学科研究手段,深入研究特定微生物、浮游生物功能类群等在大河影响下的边缘海沉积有机碳生物地球化学过程中的作用,将极大地丰富对河口和陆架边缘海生源要素生物地球化学循环的认识。 相似文献
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本文将碳同位素比值用于研究亚马孙河及其主要支流中颗粒有机碳(POC)的来源,同时也探讨了河流POC向海洋环境的输送,在亚马孙河上游POC的碳同位索值δ13C(-24.5——28.0‰)较之在其中下游的相应值(-27.9——30.1‰)要重一些一般来说,其支流POC的同位素组成要比在亚马孙河主航道中测得的值要轻一些由碳同位素数据证明,亚马孙河主航道中POC的主要来源是陆地物质,而不是河生生物,在亚马孙河口区和淡水舌中观测到POC的同位素组成有很大的变化范围(-17.5——28.4‰),这被认为是河流的POC与海洋的POC在该区域中混合作用的结果.由同位素数据可计算出河流有机碎屑沿平行于河流航道方向向海可搬运至距河口290km处,而沿亚马孙河淡水舌方向在河口西北方向1100km处仍可看到河流POC的稳定同位素信号. 相似文献
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研究表明,海洋沉积物中有超过20%的有机碳是通过与铁结合而被稳定地保存下来,阐明铁对有机碳的保护作用能深入理解碳封存机制。本文1)从与铁结合的有机碳的含量、碳同位素和二者的结合机制等方面梳理了铁在促进有机碳埋藏中所发挥的作用;2)阐述海洋环境(包括水动力和氧化还原条件)和有机碳来源等因素可能控制着铁与有机碳之间的相互耦合,并影响着与铁结合的有机碳的分布、组成和年龄特征;3)分析铁与有机碳之间吸附和共沉淀的结合机制,讨论了影响二者结合方式的因素;4)探讨铁循环与碳循环之间的密切生物地球化学联系在海洋碳封存中的作用。综合梳理了沉积物中“生锈的碳汇”(rusty sink)的研究进展,对当前应对碳中和-全球气候变化具有重要意义。 相似文献
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渤海颗粒有机碳与生物硅的分布及来源 总被引：2，自引：1，他引：1
海洋碳、硅循环及其相关联的生物地球化学过程是全球环境变化的热点问题,也是海洋科学关心的重要领域。利用2012年5月和11月份对渤海海域的调查结果,对该海域颗粒有机碳和生物硅的分布特征及来源进行了讨论。主要结论为:渤海有机碳以溶解有机碳为主,具有春季高和秋季低的特征;由陆地来源和海洋自生的有机碳组成,且以海洋来源的有机碳为主。渤海生物硅分布具有明显的梯度特征,河流输入同样对其含量的影响较为突出。渤海沉积物中生物硅含量较高,明显高于中国东部陆架海。渤海表层沉积物中生物硅主要是海源的,依次由浮游藻类、植硅体和海绵骨针所构成,其中浮游藻类占62.9%,陆源植硅体占31.1%。渤海沉积物发现了来自于草本植物的植硅体,这说明了陆地产生的植硅体对海洋生物硅的贡献。 相似文献
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酸化过程对海洋沉积物中有机碳同位素分析的影响 总被引：6，自引：1，他引：5
海洋沉积物中有机碳同位素(δ13C)可以示踪海洋生态系统中有机质来源,对环境研究具有重要意义。分析沉积物中有机物的δ13C,需要对样品进行酸化,以去除无机碳的影响。由于不同来源的沉积物中无机碳的含量和组份存在差异,需要针对样品性质,优化酸化处理过程。本研究分别选取了无机碳含量不同的温带与热带河口、海湾沉积物样品,比较了3种不同酸化过程对有机物δ13C分析的影响。研究结果表明:方法1(酸洗法)中6%H_2SO_3和1mol/L H_3PO_4对无机碳含量较高的热带河口、海湾样品去除效率较低,而2mol/L HCl去除无机碳酸盐的效果较理想。方法2(酸蒸法)并不适用于无机碳含量较高的热带河口、海湾样品;而对于无机碳含量相对较低的温带河口、海湾样品,9h酸蒸较为适宜。方法3(非原位酸洗)的结果较方法1和方法2偏正,表明其对含13C丰富的有机组分破坏较小,且方法3中残留的酸对δ13C的分析没有影响。因此,方法3是去除海洋沉积物中无机碳较理想的方法。 相似文献
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河流输入的陆源有机碳在河口和陆架区的生物地球化学过程是全球碳循环的重要环节,对陆源有机质的输入量的估算是研究陆架区的生物地球化学过程的基础。黄河输沙量极大,为探究其携带的陆源有机质对陆架边缘海有机碳库的影响,以黄河河口及邻近渤海海域为研究对象,分析了表层沉积物中的木质素,结合总有机碳含量、总氮含量和有机碳稳定同位素评估了表层沉积物中有机碳的组成、来源和分布。8种木质素酚单体中,紫丁香基酚类(S)与香草基酚类(V)的含量比值S/V(0.63±0.31)和肉桂基酚类(C)与香草基酚类含量比值C/V(0.25±0.15),反映出研究区陆源有机碳主要来自草本被子植物。V系列中木质素酸(Ad)与木质素醛(Al)的比值(Ad/Al)V较高(0.53±0.14),表明陆源有机质的降解程度较高。利用稳定碳同位素比值δ13C和木质素含量Λ8相结合的土壤有机质-陆生维管植物-水生有机质三端元模型对陆源有机物的贡献的分析结果显示,土壤有机质、陆源维管植物和水生有机质的平均贡献分别为59.9%±15.0%、7.3%±7.0%、32.8%±11.8%。土壤在陆源有机质中的贡献占有绝对优势,可能与该区域沉积物的主要源区——黄土高原植被覆盖率低、土壤侵蚀严重有关。 相似文献
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黄、渤海沉积物中陆源脂类有机质的组成分布与转化特征 总被引：2，自引：0，他引：2
本文对黄、渤海表层沉积物中脂类化合物的组成进行了分析研究。结果表明,黄、渤海表层沉积物有机碳的含量为0.03%~1.02%,以黄河口含量最低,黄河口外和双台子河口外,以及北黄海和南黄海中部含量较高。有机质碳稳定同位素δ13C的分布为-21.55‰~-24.28‰,表征其陆海双重来源特征,并且海源特征由河口向海、由近岸向离岸逐渐增强。陆源脂类化合物以河口处略高,河道处略低,由河口向渤海中部和靠近渤海海峡方向迅速降低,表现出显著的河流输入特征;其形态组成由河道的游离态接近100%的绝对优势,迅速转变为渤海中部的以皂化结合态为主（大于50%）,仅在渤海中部和渤海海峡附近存在小于5%的矿物结合态,转化程度较低。北黄海中部和南黄海中部泥质区的有机碳和陆源脂类化合物显著富集,但其对总有机碳的相对贡献较小;其中皂化结合态超过50%,矿物结合态小于10%,说明其具有中等偏高的转化程度。 相似文献
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南沙海洋柱状沉积物的有机地球化学研究 总被引：6，自引：1，他引：6
研究了南沙海域ＮＳ９０－１０３柱样有机碳含量，各类生物标志化合物的组成和分布及其地球化学意义。结果表明，该柱样中有机碳含量高于南沙海域其他沉积环境，这表明南沙海域中大陆坡最适合于有机质的聚集。各类生物标志化合物组成和分布指示了沉积有机质主要起源于海洋浮游生牧细菌，其次为陆源高等植物，气溶胶输入可能是后者来源的途径之一；沉积环境具有强原还性；有机质处于未成熟阶段，并存在较好的成岩变化。 相似文献
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稳定碳、氮同位素在河流系统研究中的应用 总被引：13，自引：0，他引：13
对天然存在的稳定碳、氮同位素在河流系统中的有机物质(POM和DOM)来源、转换和运移规律及其与沿岸生态系统的关系、河口区不同来源颗粒有机质的混合过程、河流系统中富营养化的污染来源和土壤中的微生物过程、系统中的营养行为和食物来源途径以及河流有机物质在陆架上的分配、积累和运移规律的应用研究作了较为系统的论述。 相似文献
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M. Giani D. Berto F. Rampazzo F. Savelli F. Alvisi P. Giordano M. Ravaioli F. Frascari 《Estuarine, Coastal and Shelf Science》2009,84(4):573-583
In order to evaluate the origin and the transformation of organic matter on the shallow shelf of the NW Adriatic Sea, organic carbon, total nitrogen and stable isotope ratios of organic carbon were analysed in riverine suspended matter and sediments as well as in marine suspended and sedimentary organic matter, in marine phytoplankton and zooplankton.The deposition of organic matter is influenced by fine sediment concentration. Surface sediments were characterised by highly variable biogeochemical conditions on the sea floor, whereas sub-surface sediments showed a more homogeneous hypoxic/anoxic environment.Low Corg/N ratio and high organic carbon and nitrogen concentrations in riverine suspended organic matter indicate an important contribution of freshwater phytoplankton within rivers, particularly during low flow regimes, which adds to the marine phyto- and zooplankton at shelf locations.In order to evaluate the importance of terrestrial, riverine and marine sources of OM in shelf sediments, a three end-member mixing model was applied to shelf surface sediments using 13C/12C values for organic matter and N/C ratios. The model showed an elevated contribution of terrestrial organic substances at intermediate depths (10–15 m), mostly corresponding to an area of coarser grain-size, whereas the riverine and marine organic fractions were mainly accumulating near the coast and offshore, respectively. 相似文献
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海草床具有重要的生态系统服务功能,可以为海洋生物提供栖息地和食物来源,同时还具有重要的碳储存功能,海草床“蓝碳”功能日益受到学术界的重视,据研究全球每年海草床的碳埋藏量高达(2.7~4.4)×107 MgC。近年来,由于人类活动的影响,世界范围内海草床衰退严重,导致海草床沉积物有机碳储量降低。本文综述了全球海草床沉积物有机碳的来源、组分、储量以及指示作用;从物理、化学和生物三方面讨论了影响海草床碳储量的环境因素。最后提出了未来主要研究方向,主要包括加强海草床碳通量普查,分析全球气候变化背景下海草床沉积物有机碳的变化机制,明确海草床碳储量流失速率,研究海岸带工程对海草床沉积物有机碳的影响。评估海草床沉积物有机碳储量及变化机制可以为全球海洋蓝碳研究提供科学依据。 相似文献
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全球范围内有植被定植的海岸带栖息地(红树林、盐沼和海草床)是巨大的沉积物有机碳碳库，同时也是自然生态系统中最密集的碳汇之一，在全球碳循环中发挥着重要作用。针对江苏盐城海岸盐沼湿地沉积物有机碳的研究，区域上的稀疏性和偏向性限制了其作为区域碳汇能力的可靠估计。本研究采用47个100 cm深沉积柱样的现场调查数据，探讨了江苏盐城海岸盐沼湿地沉积物有机碳含量、密度和储量特征。结果表明，0～100 cm深度沉积物有机碳平均含量和平均密度分别为1.68%和23.07 kg/m3，不同盐沼群落沉积物有机碳含量和密度存在一定的差异，其中有机碳平均含量大小排序依次为互花米草>芦苇>盐地碱蓬，有机碳密度排序为芦苇>互花米草>盐地碱蓬。总体而言，3种盐沼群落沉积物有机碳含量的垂向变化趋势与有机碳密度变化趋势具有一致性，芦苇和互花米草表聚性明显。沉积物有机碳含量与其理化性质有关，互花米草群落沉积物有机碳含量具有明显的粒度控制效应，而其他群落不显著。3种盐沼湿地类型0～100 cm深度沉积物总碳储量约为6195.27×103Mg C。研究成果揭... 相似文献
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本文测定了海南儋州湾南岸柱状沉积物的粒度、总有机质参数(TOC、C/N和δ13C)和类脂生物标志物含量,并通过端元混合模型使用红树植物特征标志物蒲公英萜醇含量、长链正构烷烃含量和δ13C值半定量区分了海南儋州湾南岸沉积有机质来源,尤其是红树林的贡献。另外,通过估算沉积物的有机碳储量来评估儋州湾红树林区域的储碳能力。在沉积有机质中,陆源、水源和红树植物有机质所占平均比例分别为47%,36%和17%。沉积物柱状样中单位厘米深度沉积物的碳储量范围在0.12~2.90 t/ha。本研究表明,儋州湾地区沉积物中来自于红树林的有机质比例较低,且其碳埋藏量可能低于全球平均水平。修复和保护儋州湾红树林,能够有效提升湿地的碳埋藏效率,从而减缓大气CO2上升对环境的负面影响。本文应用生物标志物和碳同位素方法,半定量区分了红树林生态系统各种来源有机碳的贡献,将蒲公英萜醇作为红树林特征生物标志物应用在计算模型中,能够量化红树植物来源有机碳的贡献,加深对红树林系统有机碳埋藏情况的了解。 相似文献
17.
Sarah A. Bennett Peter J. StathamDarryl R.H. Green Nadine Le BrisJill M. McDermott Florencia PradoOlivier J. Rouxel Karen Von Damm Christopher R. German 《Deep Sea Research Part I: Oceanographic Research Papers》2011,58(9):922-931
Chemoautotrophic production in seafloor hydrothermal systems has the potential to provide an important source of organic carbon that is exported to the surrounding deep-ocean. While hydrothermal plumes may export carbon, entrained from chimney walls and biologically rich diffuse flow areas, away from sites of venting they also have the potential to provide an environment for in-situ carbon fixation. In this study, we have followed the fate of dissolved and particulate organic carbon (DOC and POC) as it is dispersed through and settles beneath a hydrothermal plume system at 9°50′N on the East Pacific Rise. Concentrations of both DOC and POC are elevated in buoyant plume samples that were collected directly above sites of active venting using both DSV Alvin and a CTD-rosette. Similar levels of POC enrichment are also observed in the dispersing non-buoyant plume, ∼500 m downstream from the vent-site. Further, sediment-trap samples collected beneath the same dispersing plume system, show evidence for a close coupling between organic carbon and Fe oxyhydroxide fluxes. We propose, therefore, a process that concentrates POC into hydrothermal plumes as they disperse through the deep-ocean. This is most probably the result of some combination of preferential adsorption of organic carbon onto Fe-oxyhydroxides and/or microbial activity that preferentially concentrates organic carbon in association with Fe-oxyhydroxides (e.g. through the microbial oxidation of Fe(II) and Fe sulfides). This potential for biological production and consumption within hydrothermal plumes highlights the importance of a multidisciplinary approach to understanding the role of the carbon cycle in deep-sea hydrothermal systems as well as the role that hydrothermal systems may play in regulating global deep-ocean carbon budgets. 相似文献
18.
L.E. Fox 《Estuarine, Coastal and Shelf Science》1983,16(4):431-440
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
19.
Fluxes and sources of suspended organic matter in an estuarine turbidity maximum region during low discharge conditions 总被引：6，自引：1，他引：6
Miguel A. Goni Mary W. Cathey Yong H. Kim George Voulgaris 《Estuarine, Coastal and Shelf Science》2005,63(4):683-700
Water column concentrations of total suspended solids (TSS), particulate organic carbon (POC) and particulate nitrogen (PN) were measured at three different depths in four different locations bracketing the estuarine turbidity maximum (ETM) along the main channel of a temperate riverine estuary (Winyah Bay, South Carolina, USA). Measurements were carried out over full tidal cycle (over 24 h). Salinity, temperature, current magnitude and direction were also monitored at the same time throughout the water column. Tidally averaged net fluxes of salt, TSS, POC and PN were calculated by combining the current measurements with the concentration data. Under the extreme low river discharge conditions that characterized the study period, net landward fluxes of salt were measured in the lower part of the study area, suggesting that the landward transport through the main channel of the estuary was probably balanced by export out through the sides. In contrast, the net fluxes of salt in the upper reaches of the study area were near zero, indicating a closed salt balance in this part of the estuary. In contrast to salt, the net fluxes of TSS, POC and PN in the deeper parts of the water column were consistently landward at all four sites in Winyah Bay indicating the non-conservative behavior of particulate components and their active transport up the estuary in the region around the ETM.The carbon contents (%POC), carbon:nitrogen ratios (org[C:N]a) and stable carbon isotopic compositions (δ13CPOC) of the suspended particles varied significantly with depth, location and tidal stage. Tidally averaged compositions showed a significant increase up the estuary in the %POC and org[C:N]a values of suspended particles consistent with the preferential landward transport of carbon-rich particles with higher vascular plant debris content. The combination of tidal resuspension and flood-dominated flow appeared to be responsible for the hydrodynamic sorting of particles along the estuary that resulted in denser, organic-poor particles being transported landward less efficiently. The elemental and isotopic compositions indicated that vascular C3 plants and estuarine algae were the major sources of the particulate organic matter of all the samples, without any significant contributions from salt marsh C4 vegetation (Spartina alterniflora) and/or marine phytoplankton. 相似文献
20.
In order to investigate the photobleaching potential of estuarine waters from different depths and redox conditions and with varying degree of biological activity, filtered, unfiltered and chloroform-poisoned water samples from the Baltic Sea were exposed to ambient sunlight. Fluorescence, at excitation 350 nm and emission 450 nm, was used as an indication of humic substance concentration. Fluorescence and organic carbon concentration were measured at regular time intervals during light exposure. We found that the decrease in humic substance fluorescence can be fitted to an exponential decay function. The fluorescence half-lives were within the range 0.4 – 4.6 days in different water masses, with fluorescence decreasing to between 20% and 60% of initial concentration, respectively. Results from the curve fitting procedure indicate a rest concentration of humic substance fluorescence, similar among the sampled sites, that is resistant to further photochemical degradation. The largest relative decreases in fluorescence were found in deep waters, but samples from deep waters also had a higher fluorescence rest concentration than samples from surface waters. Biological activity was reduced by filtering the samples through 0.2μm pore size filters or adding chloroform. No statistically significant differences were found after 3 days of irradiation between samples with and without treatment to reduce biological activity. The highest initial fluorescence values and the largest fluorescence decrease were found in the anoxic waters of the Gotland Deep. The organic carbon concentrations decreased 3–7% at all stations. The shortest half-life of humic substance, and the largest decrease in organic carbon concentrations, were found in samples from the northern basins of the Baltic Sea. 相似文献