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1.
铁在地壳中的含量位列第四,在海洋中常以微量元素的身份出现。铁拥有多变的价态和多样的功能,是调节海洋初级生产力和驱动海洋生物地球化学循环的重要力量。以往的研究表明,铁在维持初级生产力、耦合物质循环以及调节生源要素转化中具有重要作用。近年来微生物生态学的发展将铁的研究推向了新的高度,包括微生物驱动的铁氧化-还原行为、代谢过程以及与主要元素(C/N/P)的交互关系等。以近15年发表的文献为重点,尝试综述铁的最新进展。首先梳理了海洋中铁的来源和赋存状态(溶解态、胶体态、颗粒态和有机态);其次阐释了微生物介导的铁氧化还原类型和过程机制(如硝酸盐氧化、生物还原等);最后总结了铁与C/N/P循环的耦合关系以及在特定生态事件中的生态效应。此外,对海洋铁研究的“化学-生物-物理”理论框架也进行了展望,旨在为更好地认识铁循环及其在海洋微生态过程的作用提供资料借鉴。  相似文献   

2.
铁元素对海相沉积物早期成岩作用的影响   总被引:1,自引:0,他引:1  
铁元素是地壳中丰度最高的元素之一,在海相沉积物成岩过程中起着非常重要的作用.铁元素作为海洋初级生产力的微营养元素,影响海相沉积物中有机质的输入,其在早期成岩阶段与硫化物和磷元素的耦合关系,可以促进或者降低有机质的保存;铁元素在海相沉积物早期成岩过程中可以改变孔隙水的化学性质,影响亚稳定碳酸盐矿物的保存,导致碳酸盐沉积物...  相似文献   

3.
具有生物活性的元素Fe被认为限制了海洋生物生产力,其在海洋生态系统中的生物地球化学循环对全球碳循环起到调节作用,全球40%~50%的海洋因“高叶绿素低营养盐”(HNLC)“缺Fe”而初级生产力较低.然而,关于生物活性元素Fe的研究不仅涉及海洋科学,还与大气科学、环境科学、地球科学等学科紧密联系.近些年,围绕生物活性元素“Fe”开展的研究不仅是地球科学领域的前沿问题,还是海洋学家与环境学家共同关注的热点问题.目前,尽管对于生物活性元素Fe的研究已取得很大的进展,但模型、室内实验及野外观测之间仍存在很大的挑战与不确定性.系统地总结了生物活性元素Fe最重要的自然来源方式,详细介绍了影响生物活性元素Fe溶解度的主要因素,最后,对将来的工作提出建议,为我国未来开展类似的研究提供参考.  相似文献   

4.
We present a model of the global biogeochemical cycle of silicon (Si) that emphasizes its linkages to the carbon cycle and temperature. The Si cycle is a crucial part of global nutrient biogeochemistry regulating long-term atmospheric CO2 concentrations due to silicate mineral weathering reactions involving the uptake of atmospheric CO2 and production of riverine dissolved silica, cations and bicarbonate. In addition and importantly, the Si cycle is strongly coupled to the other nutrient cycles of N, P, and Fe; hence siliceous organisms represent a significant fraction of global primary productivity and biomass. Human perturbations involving land-use changes, burning of fossil fuel, and inorganic N and P fertilization have greatly altered the terrestrial Si cycle, changing the river discharge of Si and consequently impacting marine primary productivity primarily in coastal ocean waters.  相似文献   

5.
海洋硅循环是海洋生物地球化学循环的关键过程之一,对调控全球二氧化碳浓度、海洋酸碱度和多种元素(氮、磷、铁、铝等)的循环具有重要作用。在当今气候变化和人类活动影响日益增强的背景下,硅循环与“生物泵”及碳循环的紧密联系,是其成为地球科学领域研究热点的主要原因。海洋中硅的外部来源主要为河流、地下水、大气沉降、海底玄武岩风化作用和海底热液输送5个途径,在全球气温变暖趋势的影响下,极地冰川融化成为高纬度海域不可忽视的硅源。生物硅在沉积物中的埋藏、硅质海绵和生物硅的反风化作用是重要的海洋硅移除过程。海洋硅循环过程复杂,受生物(生物吸收、降解)、物理(吸附、溶解)和化学(矿化分解和反风化作用)多重因素的影响,针对海洋硅循环关键过程的研究有助于综合评估海洋硅的“源-汇”和收支。本文总结了海洋硅循环的主要过程及海洋硅的收支,根据国际和国内研究现状讨论了当前海洋硅循环研究中面临的主要问题和挑战。现有研究成果显示,海洋硅的外源输入和输出通量比以往的评估分别增加了2.4和2.2倍。在短时间尺度内(<8 ka),全球海洋中硅的收支大致平衡,海洋硅循环基本处于稳定状态。气候变化和人类活动导致河流输送至陆架边缘海的硅通量发生变化,可能影响硅藻等海洋浮游植物种群结构,是未来海洋硅循环研究需要关注的问题之一。陆架边缘海较高沉积速率和强烈的反风化作用提高了该区域生物硅的埋藏效率,准确评估该区域生物硅的埋藏通量仍是亟须解决的难题。目前的研究评估了全球海洋浮游硅藻、硅质海绵以及放射虫生产力,而海洋底栖硅藻生产力的贡献受到忽视,未来需要关注底栖硅藻对生物硅的贡献及其在海洋硅的生物地球化学过程中的作用。  相似文献   

6.
李超  舒劲松  许斐  杨守业 《地球科学》2013,38(3):454-460
元素铁因其在地球早期环境演化和在海洋初级生产力中的重要角色, 是目前全球变化与地球化学研究的热点.铁元素的相态分析, 对于深入了解其在环境中迁移、转化及生物的吸收利用, 都具有重要意义.回顾沉积物中铁的化学相态分析方法发展过程, 从早期的简单相态分析(degree of pyritization, DOP), 元素的顺序提取法(Tesser方法), 到Raiswell和Poulton等学者提出针对Fe元素特定的相态分析法等.重点介绍较为常用的三步提取法和其在表生地球化学研究中的应用; 结合目前国际上铁地球化学循环研究进展, 提出Fe的化学相态分析的改进建议.   相似文献   

7.
Trace elements serve important roles as regulators of ocean processes including marine ecosystem dynamics and carbon cycling. The role of iron, for instance, is well known as a limiting micronutrient in the surface ocean. Several other trace elements also play crucial roles in ecosystem function and their supply therefore controls the structure, and possibly the productivity, of marine ecosystems. Understanding the biogeochemical cycling of these micronutrients requires knowledge of their diverse sources and sinks, as well as their transport and chemical form in the ocean.Much of what is known about past ocean conditions, and therefore about the processes driving global climate change, is derived from trace-element and isotope patterns recorded in marine deposits. Reading the geochemical information archived in marine sediments informs us about past changes in fundamental ocean conditions such as temperature, salinity, pH, carbon chemistry, ocean circulation and biological productivity. These records provide our principal source of information about the ocean's role in past climate change. Understanding this role offers unique insights into the future consequences of global change.The cycle of many trace elements and isotopes has been significantly impacted by human activity. Some of these are harmful to the natural and human environment due to their toxicity and/or radioactivity. Understanding the processes that control the transport and fate of these contaminants is an important aspect of protecting the ocean environment. Such understanding requires accurate knowledge of the natural biogeochemical cycling of these elements so that changes due to human activity can be put in context.Despite the recognised importance of understanding the geochemical cycles of trace elements and isotopes, limited knowledge of their sources and sinks in the ocean and the rates and mechanisms governing their internal cycling, constrains their application to illuminating the problems outlined above. Marine geochemists are poised to make significant progress in trace-element biogeochemistry. Advances in clean sampling protocols and analytical techniques provide unprecedented capability for high-density sampling and measurement of a wide range of trace elements and isotopes which can be combined with new modelling strategies that have evolved from the World Ocean Circulation Experiment (WOCE) and Joint Global Ocean Flux Study (JGOFS) programmes. A major new international research programme, GEOTRACES, has now been developed as a result of community input to study the global marine biogeochemical cycles of trace elements and their isotopes. Here, we describe this programme and its rationale.  相似文献   

8.
River damming transforms allotropic natural rivers into autotrophic 'impound river' (referred to "reservoir"), which changes the processes of river biogenic substance cycle and the matter properties as well as export flux from land to ocean, thus becoming one of the key problems of element biogeochemical cycle. Due to the different behavior of biogenic substances (C, N, P, Si) in biological processes, biogenic substances cycle efficiency is different, in turns, Silicon (Si)>Organic Carbon (OC)>Phosphorus (P). The migration and transformation processes of C and Si are significantly affected by phytoplankton and water retention time. Nitrogen (N) and P are mainly affected by water pH, temperature, Dissolved Oxygen (DO) and retention time. The retention efficiency of biogenic substances is shown as N>C>P>Si at the global scale. Besides, the sedimentation and burial processes of reservoirs constitute the net sink of OC in rivers. River damming alters the stoichiometric characteristics of water elements, nutrient constraints, aquatic communities composition and the coupling effect of C/N/P/Si. The stable isotopic compositions of C, N and Si can effectively trace the source, migration and transformation of biogenic matter. A combination of elements stoichiometric characteristics and stable isotopic composition could effectively indicate the change of source materials in reservoirs. With the increasing demand for clean energy, the intensity of river damming and reservoir construction will increase. Thus, a series of scientific problems including changing law of biogenic substance migration and transformation dynamic, as well as accumulation effect of ecological environment in watershed systems by river cascade damming, should need to be concerned in the biogeochemistry cycle study.  相似文献   

9.
黄永建  王成善 《地学前缘》2009,16(5):172-180
铁作为地壳中丰度最高的元素之一,广泛参与到一系列地球化学循环中。现代海洋中的铁主要来源于河流、冰川和风的铁氧化物颗粒和溶解铁的输入。陆源输入的铁氧化物在有机质埋藏、降解的早期成岩作用过程中,发生一系列转化过程而埋藏下来,该过程被称作活性铁循环。氧化 强氧化条件利于沉积物中氧化铁的持续产生或者至少保持不被溶解的状态,从而形成棕色-红色沉积物;还原条件利于沉积物中铁氧化物的溶解,形成菱铁矿、黄铁矿(铁硫化物) 等形式的埋藏,并可能造成溶解铁在海洋内的迁移。Raiswell、Canfield、Poulton等通过对现代典型海洋环境活性铁循环研究,提出了一系列用于判别古海洋氧化 还原条件的活性铁指标体系,并成功地将太古宙以来的古海洋划分成为含铁的大洋、硫化的大洋和氧化的大洋等3个演化阶段。由于活性铁的不同形态对磷具有不同的生物地球化学效应,将造成“氧化条件下磷的优先埋藏、缺氧条件下优先释放的现象”。磷是海洋生产力的限制性元素,铁和磷循环的上述耦合关系将造成“缺氧的大洋生产力越高,富氧的大洋生产力越低”现象的出现。目前已在白垩纪古海洋缺氧 富氧沉积中初步证实了上述反馈关系的存在,但是对活性铁埋藏形式对该特殊沉积的贡献还需要进一步的工作。  相似文献   

10.
Fe是海洋“生物泵”中限制浮游生物生长和控制海洋初级生产力的主要因素之一,也可间接影响大气中CO2含量,反馈于全球的气候变化。近年来基于多接收电感耦合等离子体质谱仪(MC ICP MS)分析方法的改进及测试精度的提高,应用Fe同位素组成、变化及其分馏机制,为研究海水中Fe的主要来源以及示踪海洋环境中Fe的循环过程等,提供了一个有效地球化学指标,也对示踪地球不同演化阶段的海洋沉积环境变化具有指示意义。较为详细地介绍了海洋环境中不同储库的Fe同位素组成,洋中脊热液流体—玄武岩、海水—大洋玄武岩等水—岩反应影响Fe同位素分馏效应的主要因素及地球不同演化阶段古海洋沉积环境中的Fe同位素变化。认为海洋环境下Fe同位素可以产生较为明显的分馏作用,轻铁同位素具有更易活动、易迁移的特征,并进一步提出不同相态、不同矿物间Fe同位素分馏系数的确定等相关问题仍是今后Fe同位素研究的主要方向。  相似文献   

11.
文章在AMS~14C定年的基础上建立了南海北部MD05-2905钻孔(20°08.17′N,117°21.61′E)末次冰期以来有机地球化学记录的时间序列,利用其中的正构烷烃、甾醇和烯酮等有机分子标志物对南海北坡25ka以来沉积物物源、气候环境变化进行探讨。长链正构烷烃总含量和浮游植物标志物总含量表明25.0~14.5kaB.P.时段南海北部沉积物中陆源物质输入、海洋初级生产力浮游植物输入均较高,14.5~8.5kaB.P.时段迅速降低,全新世8.5kaB.P.之后稳定在较低水平。末次冰期海平面低,陆架出露面积大,陆源物质搬运至沉积地点的距离短,强盛的冬季风及其驱动的洋流有利于大量的陆源物质搬运至该沉积地点;14.5kaB.P.,对应于MWPIa时期,陆源物质输入迅速减少,海洋初级生产力的迅速降低,印证了此时海平面的快速上升。C31/C17物源参数表明陆源物质输入和海洋内生源输入在25.0~14.5kaB.P.时段和14.5~8.5kaB.P.时段分别占据了主要地位,这表明海平面变化对陆源物质输入影响可能更大;全新世8.5ka之后,陆源、海洋内生源输入交替占据主要地位,这可能与东亚季风增强有关。从有机分子标志物研究来看,海平面的变化对陆源物质输入及总海洋初级生产力可能均有重要控制作用,但海洋初级生产力中某些藻类如硅藻可能受控于不同的气候因素。C28甾醇含量指示硅藻在MWPIa和MWPIb时期大量增多,这可能是14.5~8.5kaB.P.海洋内生源输入相对较多的重要原因,同时,对11.0~8.5kaB.P.时段的碳酸钙低值事件可能有一定贡献,但其对海陆环境的响应还有待于进一步研究。  相似文献   

12.
Understanding the mechanisms responsible for long-term storage of organic carbon (OC) in marine environment is important for studying the marine carbon cycling and predicting how the global carbon cycle will respond to climate change. It is estimated that more than 20% of the OC in marine sediments is associated with iron oxides and thus these complexes are one of the most important factors in the long-term storage of OC. The OC-iron oxide (OC-Fe) association can be formed through either adsorption or co-precipitation, but the dominant mechanism of OC-Fe association in marine environments is co-precipitation. The combination of OC from different sources with iron oxides is selective. Iron oxides preferentially combine with marine OC in most marine environments, but in estuarine delta regions they prefer terrestrial OC. Due to large inputs of terrestrial materials, high primary production and frequent re-suspension, estuarine and marginal seas are suitable sites for OC-Fe association studies, which should be emphasized in the future.  相似文献   

13.
Dissolved iron profiles along a north-south transect along 158°W in the tropical Pacific show evidence of two deepwater anomalies. The first extends from Station ALOHA (22.78°N) to the equator at ∼1000-1500 m and lies below the maximum apparent oxygen utilization and nutrient (N, P) concentrations. The feature is not supported by vertical export processes, but instead corresponds with the lateral dilution field of δ3He derived from the Loihi seamount, Hawaii, though a sediment source associated with the Hawaiian Island Chain cannot be entirely ruled out. The second, deeper (2000-3000 m) anomaly occurs in tropical South Pacific waters (7°S) and also does not correlate with the depths of maximum nutrient concentrations or apparent oxygen utilization, but it does coincide closely with δ3He emanating from the East Pacific Rise, more than 5000 km to the east. We hypothesize that these anomalies represent the long-range (>2000 km) transport of hydrothermal iron residuals, stabilized against scavenging by complexation with excess organic ligands in the plume source regions. Such trace leakage of hydrothermal iron to distal plume regions would have been difficult to identify in most hydrothermal vent mapping studies because low analytical detection limits were not needed for the proximal plume regions. These findings suggest that hydrothermal activity may represent a major source of dissolved iron throughout the South Pacific deep basin today, as well as other regions having high mid-ocean spreading rates in the geologic past. In particular, we hypothesize that high spreading rates along the South Atlantic and Southern Ocean mid-oceanic ridges, combined with the upwelling ventilation of these distal hydrothermal plumes, may have increased ocean productivity and carbon export in the Southern Ocean. Assessing the magnitude and persistence of dissolved hydrothermal iron in basin scale deep waters will be important for understanding the marine biogeochemistry of iron and, potentially, on ocean productivity and climate change during the geologic past.  相似文献   

14.
王先美 《地质学报》2008,82(1):1258-1273
鲁西隆起区发育有大量的北西向脆性断裂。依据野外断裂构造的几何学、运动学详细解析认为,北西向断裂系经历了早期的右行压剪、右行张剪,以及后期的左行压剪等不同性质的构造活动。由与北西向断裂活动相伴生的同期侵入岩体的 K-Ar测试结果分析,北西向断裂系在距今约160 Ma及距今130~110 Ma分别经历了右行压剪与右行张剪构造活动;通过分布在隆起区不同样品的磷灰石裂变径迹数据分析、冷却史反演,厘定鲁西地体在距今90~80 Ma存在一次区域性快速冷却构造事件,该构造事件与北西向断裂系的左行压剪构造活动相对应。  相似文献   

15.
王先美 《地质学报》2008,82(9):1258-1273
鲁西隆起区发育有大量的北西向脆性断裂.依据野外断裂构造的几何学、运动学详细解析,认为北西向断裂系经历了早期的右行压剪、右行张剪,以及后期的左行压剪等不同性质的构造活动.由与北西向断裂活动相伴生的同期侵入岩体的 K-Ar测试结果分析,北西向断裂系在距今约160 Ma及距今130~110 Ma分别经历了右行压剪与右行张剪构造活动;通过分布在隆起区不同样品的磷灰石裂变径迹数据分析、冷却史反演,厘定鲁西地体在距今90~80 Ma存在一次区域性快速冷却构造事件,该构造事件与北西向断裂系的左行压剪构造活动相对应.  相似文献   

16.
Microplastics in the ocean are the plastic fragments less than 5 mm in diameter, which enter into the ocean through a variety of ways. In the past 60 years, the global plastic production increased by 560 times, and the accumulation of microplastics in the marine environment is increasing. Microplastics suspend in seawater, or deposit to the bottom sediments. The potential risks of microplastics to marine ecosystems cause widespread concern. This paper summarized the research progress of the ecological risks of microplastics in the ocean, including the distribution and concentration of marine microplastics in coastal waters, sediment and open ocean, the ingestion of microplastics by different species of marine organisms, the ecotoxicology of microplastics, the plastics additives and the absorbed pollutants. The research directions were proposed for the future, including the optimization of microplastics sampling and measuring methods, microplastics observation in different marine habitats, the eco-toxicological effects of microplastics and food chain bioaccumulation effect, the methodology of microplastics ecological risk assessment. It is expected to provide evidence for the risk assessment of microplastics on Chinese coastal ecosystems.  相似文献   

17.
Detailed investigations of high latitude sequences recently collected by the Ocean Drilling Program (ODP) indicate that periods of rapid climate change often culminated in brief transient climates, with more extreme conditions than subsequent long term climates. Two examples of such events have been identified in the Paleogene; the first in latest Paleocene time in the middle of a warming trend that began several million years earlier: the second in earliest Oligocene time near the end of a Middle Eocene to Late Oligocene global cooling trend. Superimposed on the earlier event was a sudden and extreme warming of both high latitude sea surface and deep ocean waters. Imbedded in the latter transition was an abrupt decline in high latitude temperatures and the brief appearance of a full size continental ice-sheet on Antarctica. In both cases the climate extremes were not stable, lasting for less than a few hundred thousand years, indicating a temporary or transient climate state. Geochemical and sedimentological evidence suggest that both Paleogene climate events were accompanied by reorganizations in ocean circulation, and major perturbations in marine productivity and the global carbon cycle. The Paleocene-Eocene thermal maximum was marked by reduced oceanic turnover and decreases in global delta 13C and in marine productivity, while the Early Oligocene glacial maximum was accompanied by intensification of deep ocean circulation and elevated delta 13C and productivity. It has been suggested that sudden changes in climate and/or ocean circulation might occur as a result of gradual forcing as certain physical thresholds are exceeded. We investigate the possibility that sudden reorganizations in ocean and/or atmosphere circulation during these abrupt transitions generated short-term positive feedbacks that briefly sustained these transient climatic states.  相似文献   

18.
We present a model of estuarine mixing, removal, and input for dissolved constituents, and apply the model to 39 nutrient (P, N, Si) profiles collected over a 14-month period in a pristine river/ estuary: Ochlockonee Bay, Florida. Each profile is deconvolved into three component functions: linear mixing (conservative) first-order removal (biological productivity), and parabolic input (regeneration). After correction for temporal variations in the fluvial end-members, the model provides quantitative estimates of total estuarine primary production, net regeneration, and subsequent fluxes to the ocean over a year-long period. The modeled data set is internally self-consistent: virtually perfect mass balances are obtained for P and Si. All biological P-uptake is regenerated within the estuary so that virtually 100% of the fluvial reactive-P enters the ocean. One-third of the fluvial reactive-P enters the estuary as particles whose phosphate is released after deposition in estuarine sediments. About 20% of the dissolved fluvial silica flux is removed biologically; all of this biogenic silica dissolves in the estuary and enters the ocean. N cannot be mass balanced, probably because it enters and escapes the bay in unmeasured forms (as NH4 or via denitrification to N2 and N2O). In the Ochlockonee, biological productivity removes nutrients in the ratios N:P ? 9:1 and Si:P ? 20:1.  相似文献   

19.
镉稳定同位素研究进展   总被引:1,自引:1,他引:0  
Cd具有挥发性和亲硫性,在海洋环境中Cd为微量营养元素,而在生态环境及农业土壤环境中Cd为有毒元素.因此,镉同位素被应用于海洋科学、地球科学、环境科学及农业科学研究,并展现出巨大的应用潜力.本文总结了近年来富含有机质的环境样品、植物样品和生物样品的消解方法,以及Cd分离纯化及双稀释剂校正方法的研究进展.采用微波、高压灰...  相似文献   

20.
邬钰  向武  傅先芳  李启立  苏靖  龚文  王翰 《地球科学》2016,41(4):683-691
大量研究表明,溶解性有机质与铁的螯合对生物可利用性铁的输出有重要影响.然而,对于天然有机质,尤其是泥炭沼泽源的酚类物质,与铁相互作用的地球化学机制仍然缺乏研究.以长白山西麓哈尼泥炭沼泽为研究对象,调查了泥炭沼泽源水体可溶性总铁、亚铁、水溶性总酚等理化指标.同时,测定了泥炭中酚酸的组成及含量,分析对比泥炭与土壤中铁的主要赋存形态.并开展了酚铁相互作用模拟实验,研究了泥炭沼泽源水体中酚铁相互作用机制.结果表明:哈尼泥炭沼泽水体中亚铁浓度与水溶性总酚浓度显著相关,说明水溶性总酚对亚铁的存在及运移有重要影响.哈尼泥炭中含有原儿茶酸、咖啡酸、没食子酸、龙胆酸、丁香酸、阿魏酸、对羟基苯甲酸、对香豆酸、水杨酸、香草酸等多种酚酸.其中,具有儿茶酚或没食子酰基结构的原儿茶酸、咖啡酸和没食子酸能与亚铁形成稳定螯合物,是泥炭沼泽源水体中Fe(Ⅱ)保持稳定并可以远距离迁移的关键.研究还表明,原儿茶酸、咖啡酸、没食子酸和龙胆酸对Fe(Ⅲ)有显着的还原作用,有利于沼泽区水体中的保持较高Fe(Ⅲ)和Fe(Ⅱ)浓度.哈尼泥炭中铁主要以活动态(可交换态、络合态和无定形态)为主,为铁的迁移、转化和循环奠定了基础.鉴于泥炭沼泽在全球的分布面积巨大以及亚铁对海洋生物有促进作用,酚酸对铁的作用机制对陆地系统向海洋输送生物可利用铁具有重要意义,并对碳循环、硫循环以及气候变化有重要影响.   相似文献   

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