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1.
硅的生物地球化学循环研究进展 总被引：2，自引：0，他引：2
生命元素硅在陆地生态系统和水生生态系统中都扮演着重要的角色。它的生物地球化学循环与全球碳循环和全球气候交化密切相关。因此,近年来逐渐成为研究的热点。本文概述了近年来国内外有关硅的生物地球化学循环的研究进展,包括陆地和海洋中硅的生物地球化学循环过程及人类活动对硅循环的影响等方面,指出日前研究中存在的问题,展望了研究的重点。 相似文献
2.
《地球科学进展》2015,(1)
河流溶解硅(DSi)承载着陆地表生过程的环境信息,其输入、迁移、转化和输出受多种因素制约。在全球硅酸盐岩风化过程中,31.53%~64.87%的DSi被陆地植被吸收,仅12.91%迁移至河流,在向海洋输送过程中,河流DSi又受到水生生物吸收、逆风化作用及"人造湖效应"等因素的影响,输出量进一步减少,弱化了海洋系统的"生物泵"作用;不多的研究表明全球河流DSi浓度变化介于138~218μmol/L之间,空间差异显著,有必要量化各影响因素的贡献,建立多因素控制的河流DSi输出通量模型;与地壳主要硅酸盐岩的δ~(30)Si值(约为-0.5‰)相比,全球河流DSi的δ~(30)Si值变化范围较大(介于-0.2‰~3.4‰之间)且显著正偏,分馏系数达0.3%~3.9‰。这是由于流域内Si同位素的无机分馏和有机分馏2种动力分馏过程所导致。因此,探讨河流DSi来源、迁移及转化机制是未来深入研究河流DSi循环的关键问题。 相似文献
3.
硅元素是地球第二大组成元素,深刻影响着地表物质循环,是陆海相互作用研究、全球碳循环研究的关键元素之一.从自然风化、生物过程和人类活动3个方面综述了国内外有关地表过程对硅产出影响的研究进展,重点分析了生物过程和人类活动在硅生物地球化学循环过程中的作用.综合分析指出,应着重开展生物参与下原生/次生硅酸盐矿物风化速率的研究,重视高等植物在区域硅循环中的作用;富营养化与筑坝对于河流硅的滞留都十分重要,因筑坝产生的水库清水下泄在中下游河道产生的潜在效应很可能对河口硅输入产生重要的影响.应采用地球化学示踪技术,加强这方面的定量研究、模型研究、过程研究以及系统的综合性研究,特别是对流域地表过程的改变以及与筑坝、富营养化过程的联合作用,应进行深入的多学科交叉综合研究. 相似文献
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原生硅酸盐矿物风化产物的研究进展——以云母和长石为例 总被引：6，自引：0，他引：6
研究云母和长石等原生硅酸盐矿物的风化速率和风化产物对于深入理解土壤发生过程、营养元素循环以及全球气候变化具有重要的理论意义。本文从自然风化、人工化学风化和生物风化3方面总结了原生硅酸盐矿物风化作用及其产物的特点，重点阐述了微生物参与下的生物风化作用和生物矿化作用及其意义。野外观察和室内实验研究结果表明，微生物可以加速矿物的分解，而且其细胞表面及其产生的胞外多聚糖可以作为次生矿物成核的模板。 相似文献
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岩石矿物的微生物风化是地球表层系统最为活跃和普遍发生的地质营力之一。微生物对含钾岩石(以硅酸盐矿物为主)的风化能够释放其中的钾、硅和钙等元素,并在合适的环境条件下促进矿物元素的碳酸化沉淀,这是地表元素地球化学循环的重要环节之一。微生物对岩石的生物转化作用既涉及微生物的生长繁殖和代谢调控,也与元素的迁移转化和次生矿物的演化序列有关,具有重要研究价值。采用矿物学、微生物学和分子生物学等相结合的研究方法,有助于系统地研究微生物促进含钾硅酸盐矿物的风化并耦联碳酸化过程及其分子调控机制。研究证实,在纯培养条件下,微生物风化含钾矿物主要采用酸解、螯合、氧化还原等多种方式的协同作用,并可通过调控相关功能基因的表达来响应缺钾的环境以实现其对含钾矿物的有效风化,显然这有赖于微生物通过长期进化而形成的精细的分子调控机制。在土壤生态环境中,微生物对矿物风化的显著特征是该生态环境中微生物群落协同互作的群体作用效应。微生物碳酸酐酶参与的硅酸盐矿物风化伴随碳酸盐矿物的形成过程可能是个长期被忽视的地表碳增汇过程,对该问题的深入探索有助于进一步理解地质演化历史中微生物对碳素迁移转化的驱动机制。加入含钾硅酸盐矿粉的有机肥已经显示出其在土壤改良、作物生长和增加土壤碳汇等方面的正面应用效果,这为利用硅酸盐矿物的生物风化作用来延缓大气CO2浓度的持续升高提供了新的思路。介绍了有关微生物对含钾岩石生物转化释放钾素的分子机理及其碳汇效应方面的研究进展,以期抛砖引玉,推动该领域研究的快速发展。 相似文献
9.
岩溶生物地球化学研究的进展与问题 总被引：2，自引：1，他引：1
在CO2-水-碳酸盐岩活跃的代谢体系中,由于参与岩溶作用过程的二氧化碳来源复杂,因而研究碳酸盐岩环境中二氧化碳在生物介导下所耦联的物质循环过程及其与全球变化的关系成为岩溶生物地球化学学科的主要内容,并使其成为现代岩溶学的重要分支。在分析国内外岩溶学、地球化学、生物学等交叉学科研究成果的基础上,本文简要评述了基于岩溶生物地球化学特性的水土流失与石漠化过程,碳酸盐岩矿物在生物作用下的化学风化、元素释放规律以及控制元素循环的界面过程,碳酸盐岩区土壤－大气界面下的气体循环及其控制因素和过程,碳酸盐岩区有机污染物在环境中的来源、分布规律与降解,微型生物在岩溶水体碳循环过程中的作用等主题的主要研究进展和存在的科学问题。因此,需要以CO2为核心把岩溶环境中不同尺度上生物有机体参与的地球化学过程联系起来,但人们对生物有机体是如何通过协同作用而改变岩溶环境的,还了解得很少。如果能查明碳酸盐岩一土壤一水一生物相互作用产生的功能,岩溶生物地球化学将进一步拓展CO2-水-碳酸盐岩相耦合的岩溶作用过程,并在岩溶资源领域和全球变化领域有广阔的应用前景。因此,岩溶生物地球化学需要多学科的协同研究,特别是加强生物过程与岩溶过程的耦合研究,方能解决岩溶领域存在的生态环境问题。 相似文献
10.
《吉林大学学报(地球科学版)》2015,(Z1)
<正>新生代青藏高原的隆升导致了东亚地理格局的改变,形成了从大陆中央隆升区向周围辐射的亚洲主要水系,也导致亚洲季风系统在早中新世形成,又在约8Ma与约3Ma时强化(汪品先,2005),使得大陆流域内风化模式、风化程度、剥蚀速率等发生不同程度的改变,影响着全球大洋化学通量变化。化学风化作为地球表层生物地球化学循环的关键过程,起着联系地球表层各圈层的纽带作用,在对地球不同圈层中的元素进行再分配的同时(Lupker,et al.,2012),直接或间接地影响全球气候。因此,化学风化与各圈层相互 相似文献
11.
J.-T. Cornelis B. Delvaux L. André S. Opfergelt 《Geochimica et cosmochimica acta》2010,74(14):3913-289
The terrestrial biogenic Si (BSi) pool in the soil-plant system is ubiquitous and substantial, likely impacting the land-ocean transfer of dissolved Si (DSi). Here, we consider the mechanisms controlling DSi in forest soil in a temperate granitic ecosystem that would differ from previous works mostly focused on tropical environments. This study aims at tracing the source of DSi in forest floor leachates and in soil solutions under various tree species at homogeneous soil and climate conditions, using stable Si isotopes and Ge/Si ratios. Relative to granitic bedrock, clays minerals were enriched in 28Si and had high Ge/Si ratios, while BSi from phytoliths was also enriched in 28Si, but had a low Ge/Si ratio. Such a contrast is useful to infer the relative contribution of silicate weathering and BSi dissolution in the shallow soil on the release of DSi in forest floor leachate solutions. The δ30Si values in forest floor leachates (−1.38‰ to −2.05‰) are the lightest ever found in natural waters, and Ge/Si ratios are higher in forest floor leachates relative to soil solution. These results suggest dissolution of 28Si and Ge-enriched secondary clay minerals incorporated by bioturbation in organic-rich horizons in combination with an isotopic fractionation releasing preferentially light Si isotopes during this dissolution process. Ge/Si ratios in soil solutions are governed by incongruent weathering of primary minerals and neoformation of secondary clays minerals. Tree species influence Si-isotopic compositions and Ge/Si ratios in forest floor leachates through differing incorporation of minerals in organic horizons by bioturbation and, to a lesser extent, through differing Si recycling. 相似文献
12.
In soils, silicon released by mineral weathering can be retrieved from soil solution through clay formation, Si adsorption onto secondary oxides and plant uptake, thereby impacting the Si-isotopic signature and Ge/Si ratio of dissolved Si (DSi) exported to rivers. Here we use these proxies to study the contribution of biogenic Si (BSi) in a soil-plant system involving basaltic ash soils differing in weathering degree under intensive banana cropping. δ30Si and Ge/Si ratios were determined in bulk soils (<2 mm), sand (50-2000 μm), silt (2-50 μm), amorphous Si (ASi, 2-50 μm) and clay (<2 μm) fractions: δ30Si by MC-ICP-MS Nu Plasma in medium resolution, operating in dry plasma with Mg doping (δ30Si vs. NBS28 ± 0.12‰ ± 2σSD), Ge/Si computed after determination of Ge and Si concentrations by HR-ICP-MS and ICP-AES, respectively. Components of the ASi fraction were quantified by microscopic counting (phytoliths, diatoms, ashes). Compared to fresh ash (δ30Si = −0.38‰; Ge/Si = 2.21 μmol mol−1), soil clay fractions (<2 μm) were enriched in light Si isotopes and Ge: with increasing weathering degree, δ30Si decreased from −1.19 to −2.37‰ and Ge/Si increased from 4.10 to 5.25 μmol mol−1. Sand and silt fractions displayed δ30Si values close to fresh ash (−0.33‰) or higher due to saharian dust quartz deposition, whose contribution was evaluated by isotopic mass balance calculation. Si-isotopic signatures of bulk soils (<2 mm) were strongly governed by the relative proportions of primary and secondary minerals: the bulk soil Si-isotopic budget could be closed indicating that all the phases involved were identified. Microscopic counting highlighted a surface accumulation of banana phytoliths and a stable phytolith pool from previous forested vegetation. δ30Si and Ge/Si values of clay fractions in poorly developed volcanic soils, isotopically heavier and Ge-depleted in surface horizons, support the occurrence of a DSi source from banana phytolith dissolution, available for Si sequestration in clay-sized secondary minerals (clay minerals formation and Si adsorption onto Fe-oxide). In the soil-plant system, δ30Si and Ge/Si are thus highly relevant to trace weathering and input of DSi from phytoliths in secondary minerals, although not quantifying the net input of BSi to DSi. 相似文献
13.
Nan Ma Zhaoliang Song Baoli Wang Fushun Wang Xiaomin Yang Xiaodong Zhang Qian Hao Yuntao Wu 《中国地球化学学报》2017,36(4):626-637
Rivers link terrestrial ecosystems and marine ecosystems, and they transport large amounts of substances into oceans each year, including several forms of silicon (Si), carbon (C), and other nutrients. However, river damming affects the water flow and biogeochemical cycles of Si, C, and other nutrients through biogeochemical interacting processes. In this review, we first summarize the current understanding of the effects of river damming on the processes of biogeochemical Si cycle, especially the source, composition, and recycling process of biogenic silica (BSi). Then, we introduce dam impacts on the cycles of C and some other nutrients. Dissolved silicon in rivers is mainly released from phytolith dissolution and silicate weathering. BSi in suspended matter or sediments in most rivers mainly consists of phytoliths and mainly originates from soil erosion. However, diatom growth and deposition in many reservoirs formed by river interception may significantly increase the contribution of diatom Si to total BSi, and thus significantly influence the biogeochemical Si, C, and nutrient cycles. Yet the turnover of phytoliths and diatoms in different rivers formed by river damming is still poorly quantified. Thus, they should be further investigated to enhance our understanding about the effects of river damming on global biogeochemical Si, C and nutrient cycles. 相似文献
14.
Natalia Borrelli M. Osterrieth A. Romanelli M. F. Alvarez J. L. Cionchi H. Massone 《Environmental Earth Sciences》2012,65(2):469-480
Although phytoliths constitute part of the wetland suspended load, there are few studies focused on the quantification of
them in the biogenic silica (BSi) pool. So, the aim of this paper is both to determine BSi content (diatoms and phytoliths)
and its relationship with dissolved silica in surface waters, and the influence of soil and groundwater Si biogeochemistry
in Los Padres wetland (Buenos Aires Province, Argentina). In the basin of the Los Padres wetland, dissolved silica (DSi) concentration
is near 840 ± 232 μmol/L and 211.83 ± 275.92 μmol/L in groundwaters and surface waters, respectively. BSi represents an 5.6–22.1%
of the total suspension material, and 8–34% of the total mineralogical components of the wetland bottom sediments. DSi and
BSi vary seasonally, with highest BSi content (diatoms specifically) during the spring–summer in correlation to the lowest
DSi concentration. DSi (660–917.5 μmol/L) and phytolith (3.35–5.84%) concentrations in the inflow stream are higher than in
the wetland and its outflow stream (19.1–113 μmol/L; 0.45–3.2%, respectively), probably due to the high phytolith content
in soils, the high silica concentration in the soil solution, and the groundwater inflow. Diatom content (5–16.8%) in the
wetland and its outflow stream is higher than in the inflow stream (0.45–1.97%), controlling DSi in this system. The understanding
of the groundwater–surface water interaction in an area is a significant element for determining the different components
and the role that they play on the local biogeochemical cycle of Si. 相似文献
15.
The riverine dissolved silicon (DSi) brings environmental information on biogeochemical processes of terrestrial surface, of which the input, transferring, transformation and output are influenced by many factors. Among the weathering of global silicate rocks, 31.53%~64.87% of DSi are intercepted by terrestrial vegetation and only about 12.9% are transferred into rivers. During being transported into ocean, riverine DSi gets impacts from aquatic biological absorption, reverse weathering process and artificial lake effect. The quantity of output is further reduced, which weakens the effect of the oceanic biological pump. According to limited data, the DSi concentration of global rivers has a large variation, ranging from 138 μmol/L to 218μmol/L. It is necessary to quantify contribution rates of influencing factors and establish output models controlled by multiple factors. The δ30Si of riverine DSi ranges from -0.2‰ to 3.4‰. Comparing with the δ30Si of silicate rock, which is about -0.5‰, the fractionation factor is significantly partial to positive from 0.3‰ to 3.9‰. That is because of the occurrence of kinetic fractionation process in river basin including inorganic and organic fractionation. Thus, the key problems, sources and transformation mechanisms of riverine DSi during migration and being transported should be solved in future. 相似文献
16.
V. Desplanques L. Cary J.-C. Mouret F. Trolard G. Bourri O. Grauby J.-D. Meunier 《Journal of Geochemical Exploration》2006,88(1-3):190
We conducted a study of the biogeochemical cycle of silicon in a rice field in Camargue (France) in order to evaluate the role of biogenic silicon particles (BSi) in the cycle. Opal-A biogenic particles (phytoliths, diatoms…), which dissolve more rapidly than other forms of silicate usually present in soils, are postulated to represent the easiest bioavailable Si for rice. We found 0.03–0.06 wt.% of BSi in soils (mainly phytoliths). This value is lower than other values from the literature. Each year, the exportation of BSi from rice cultivation is 270 ± 80 kg Si ha− 1. We show that BSi input by irrigation is mostly composed of diatoms and we estimate it at 100 kg Si ha− 1 year− 1. This value is more than a third of the annual Si need for rice. The budget of the dissolved silicon (DSi) fluxes gives the following results: the atmospheric and irrigation inputs represents 1% and roughly 10%, respectively, of the annual need for rice; the drainage and infiltration outputs represent 17 ± 14 and 12 ± 9 kg Si ha− 1 year− 1, respectively; the balance of our budget shows that at least 170 kg Si ha− 1 year− 1 are exported from the soil. If we consider the soil BSi as the only source of dissolved silicon, this stock could be exhausted in 5 years. 相似文献
17.
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
18.
The geochemical composition of the terrestrial surface (without soils) and comparison with the upper continental crust 总被引：1，自引：0，他引：1
Jens Hartmann Hans H. Dürr Nils Moosdorf Michel Meybeck Stephan Kempe 《International Journal of Earth Sciences》2012,101(1):365-376
The terrestrial surface, the “skin of the earth”, is an important interface for global (geochemical) material fluxes between
major reservoirs of the Earth system: continental and oceanic crust, ocean and atmosphere. Because of a lack in knowledge
of the geochemical composition of the terrestrial surface, it is not well understood how the geochemical evolution of the
Earth’s crust is impacted by its properties. Therefore, here a first estimate of the geochemical composition of the terrestrial
surface is provided, which can be used for further analysis. The geochemical average compositions of distinct lithological
classes are calculated based on a literature review and applied to a global lithological map. Comparison with the bulk composition
of the upper continental crust shows that the geochemical composition of the terrestrial surface (below the soil horizons)
is significantly different from the assumed average of the upper continental crust. Specifically, the elements Ca, S, C, Cl
and Mg are enriched at the terrestrial surface, while Na is depleted (and probably K). Analysis of these results provide further
evidence that chemical weathering, chemical alteration of minerals in marine settings, biogeochemical processes (e.g. sulphate
reduction in sediments and biomineralization) and evaporite deposition are important for the geochemical composition of the
terrestrial surface on geological time scales. The movement of significant amounts of carbonate to the terrestrial surface
is identified as the major process for observed Ca-differences. Because abrupt and significant changes of the carbonate abundance
on the terrestrial surface are likely influencing CO2-consumption rates by chemical weathering on geological time scales and thus the carbon cycle, refined, spatially resolved
analysis is suggested. This should include the recognition of the geochemical composition of the shelf areas, now being below
sea level. 相似文献
19.
Carleton R. Bern Mark A. Brzezinski Charlotte Beucher Oliver A. Chadwick 《Geochimica et cosmochimica acta》2010,74(3):876-5891
Silicon isotope ratios (δ30Si) of bulk mineral materials in soil integrate effects from both silicon sources and processing. Here we report δ30Si values from a climate gradient of Hawaiian soils developed on 170 ka basalt and relate them to patterns of soil chemistry and mineralogy. The results demonstrate informative relationships between the mass fraction of soil Si depletion and δ30Si. In upper (<1 m deep) soil horizons along the climate gradient, Si depletion correlates with decreases of residual δ30Si values in low rainfall soils and increases in high rainfall soils. Strong positive correlation between soil δ30Si and dust-derived quartz and mica content show that both trends are largely controlled by the abundance of these weathering-resistant minerals. The data also lend support to the idea that fractionation of Si isotopes in secondary phases is controlled by partitioning of silicon between dissolved and precipitated products during the initial weathering of primary basalt. Secondary mineral δ30Si values from lower (>1 m deep) soil horizons generally correlate with the isotope fractionation predicted by a study of dissolved Si in basalt-watershed rivers and driven by preferential 28Si removal from the dissolved phase during precipitation. In contrast, after correcting for the influence of dust, secondary mineral Si depletion and δ30Si values in shallow (<1 m deep) soil horizons showed evidence of biocycling induced Si redistribution and substantially lower δ30Si values than predicted. Low δ30Si values in shallow soil horizons compared to predictions can be attributed to repeated fractionation as secondary minerals undergo additional cycles of dissolution and precipitation. Primary mineral weathering, secondary mineral weathering, dust accumulation, and biocycling are major processes in terrestrial Si cycling and these results demonstrate that each can be traced by δ30Si values interpreted in conjunction with mineralogy and measures of Si depletion. 相似文献
20.
Mirjam Kiczka Jan G. Wiederhold Jakob Frommer Stephan M. Kraemer Ruben Kretzschmar 《Geochimica et cosmochimica acta》2011,75(19):5559-5573
The chemical weathering of primary Fe-bearing minerals, such as biotite and chlorite, is a key step of soil formation and an important nutrient source for the establishment of plant and microbial life. The understanding of the relevant processes and the associated Fe isotope fractionation is therefore of major importance for the further development of stable Fe isotopes as a tracer of the biogeochemical Fe cycle in terrestrial environments. We investigated the Fe mineral transformations and associated Fe isotope fractionation in a soil chronosequence of the Swiss Alps covering 150 years of soil formation on granite. For this purpose, we combined for the first time stable Fe isotope analyses with synchrotron-based Fe-EXAFS spectroscopy, which allowed us to interpret changes in Fe isotopic composition of bulk soils, size fractions, and chemically separated Fe pools over time in terms of weathering processes. Bulk soils and rocks exhibited constant isotopic compositions along the chronosequence, whereas soil Fe pools in grain size fractions spanned a range of 0.4‰ in δ56Fe. The clay fractions (<2 μm), in which newly formed Fe(III)-(hydr)oxides contributed up to 50% of the total Fe, were significantly enriched in light Fe isotopes, whereas the isotopic composition of silt and sand fractions, containing most of the soil Fe, remained in the range described by biotite/chlorite samples and bulk soils. Iron pools separated by a sequential extraction procedure covered a range of 0.8‰ in δ56Fe. For all soils the lightest isotopic composition was observed in a 1 M NH2OH-HCl-25% acetic acid extract, targeting poorly-crystalline Fe(III)-(hydr)oxides, compared with easily leachable Fe in primary phyllosilicates (0.5 M HCl extract) and Fe in residual silicates. The combination of the Fe isotope measurements with the speciation data obtained by Fe-EXAFS spectroscopy permitted to quantitatively relate the different isotope pools forming in the soils to the mineral weathering reactions which have taken place at the field site. A kinetic isotope effect during the Fe detachment from the phyllosilicates was identified as the dominant fractionation mechanism in young weathering environments, controlling not only the light isotope signature of secondary Fe(III)-(hydr)oxides but also significantly contributing to the isotope signature of plants. The present study further revealed that this kinetic fractionation effect can persist over considerable reaction advance during chemical weathering in field systems and is not only an initial transient phenomenon. 相似文献