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1.
珠江流域碳酸盐岩与硅酸盐岩风化对大气CO_2汇的效应 总被引：6，自引：0，他引：6
对珠江流域11个测站的河水1个水文年4次取样进行水化学和同位素测试分析,揭示无论是碳酸盐岩区还是硅酸盐岩区,岩石风化均使河流的离子成分以HCO3-、Ca2+、Mg2+为主,碳酸盐岩风化溶蚀速率和由碳酸盐岩风化溶蚀引起的大气CO2消耗量分别为27.60 mm/ka和540.21x103mol/(km2·a-1),是硅酸盐岩风化速率和由硅酸盐岩风化引起的大气CO2消耗量的10.8倍和6.7倍,说明碳酸盐岩风化是流域碳汇过程及效应的主体。由于有利的水热条件和高的碳酸盐岩面积比例,珠江流域平均岩石风化速率和由岩石风化作用引起的大气CO2消耗量分别为30.15mm/ka和620.36×103mol/(km2·a-1),为全球60条河流平均值的2.6倍。 相似文献
2.
通过对四川省雅安龙苍沟峨眉山玄武岩小流域的水化学组成研究,分析了不同物质来源对小流域溪水溶解质的贡献,并对该小流域岩石风化速率和CO2消耗速率进行了估算。结果表明,龙苍沟流域溪水呈中性,PH平均值为6.82。溪水中阳离子以Ca^2+为主,约占阳离子总量的56%;阴离子以HCO3^-为主,约占阴离子总量的45%。碳酸盐岩风化、硅酸盐岩风化、大气降水和人为活动对溪水阳离子平均贡献率分别为50.2%、38.2%、10.5%和1.1%。流域硅酸盐岩风化速率为37.54±24.94 t/km^2/yr,硅酸盐岩风化对大气C02消耗速率为5.4±3.6 mol C/km^2/yr。本文首次对我国峨眉山玄武岩省化学风化大气CO2消耗量进行估算,得到其年消耗通量为1.35±0.89×10^11 mol C/yr,约为全球玄武岩CO2年消耗通量的3.31±2.18%。 相似文献
3.
硫酸参与的长江流域岩石化学风化速率与大气CO2消耗 总被引：4，自引：0，他引：4
流域的岩石化学风化过程是全球碳循环中的重要环节。以往的流域水化学碳汇通量估算大多是基于碳酸的风化作用。而实际上,硫酸和碳酸一样,也参与了流域碳元素的地球化学循环,从而对全球碳循环过程产生影响。长江流域水体近几年出现酸化现象,大部分河段SO42-和Ca2+含量增高,其对应的岩石风化过程和大气CO2消耗速率也发生变化。文章对长江干流及主要支流2013年不同季节的离子组成进行监测,利用水化学平衡法和Galy估算模型,对长江流域岩石化学风化速率和CO2消耗通量进行了估算,对硫酸参与下的长江流域岩石风化和碳循环过程进行了分析。结果表明,长江流域水体离子主要来源于硅酸盐岩风化和碳酸盐岩风化。其中碳酸盐岩风化对河水离子贡献率为92%。在硅酸盐岩广泛分布的赣江流域,碳酸盐岩风化离子贡献也达85%。分析表明,硫酸参与了长江流域的岩石风化过程,对水体中离子产生一定影响。硫酸的参与加快了碳酸盐岩的化学风化速率,平均提高约30%,但是使流域大气CO2消耗速率降低。在不考虑蒸发岩溶蚀作用下,平均从516×103 mol/km2·a降至356×103 mol/km2·a,降低约31%。在各支流中,硫酸对乌江流域碳酸盐岩的风化和碳循环的影响最大,而对雅砻江的影响最小,这与乌江流域的含煤地层、矿床硫化物及大气酸沉降有关。 相似文献
4.
中国岩石风化作用所致的碳汇能力估算 总被引：18，自引：0，他引：18
岩石的风化作用同时参与了短时间尺度和长时间尺度的全球碳循环 ,对碳酸盐岩而言 ,它的风化作用在短时间尺度上对大气二氧化碳循环具有重要影响 ,但在长时间尺度上不产生净碳汇 ;而硅酸盐岩等其他类型岩石的风化过程由于反应速率较慢 ,在短时间尺度上对全球碳循环及其变化反应不灵敏 ,但它所产生的净碳汇是遗漏汇的组成之一 .为了准确估计我国岩石风化所致的碳汇能力 ,简要评价了现有的各种模型和方法 ,并基于GEM -CO2 模型进行了计算 .计算结果表明 ,我国岩石每年因溶蚀、风化作用共消耗的CO2 约为 4 .72× 10 7t,折合成C为 1.4 1× 10 7t,其中由碳酸盐类岩石风化消耗的碳量最多 ,约为 0 .74× 10 7t/a ,占总量的 5 2 .6 5 % .硅酸盐岩及其他类型岩石风化消耗的碳量约为 0 .6 7× 10 7t/a ,占总量的 4 7.35 % .岩石风化所致碳汇能力的空间分布首先取决于岩石类型 ,其次受地区的气候条件控制 . 相似文献
5.
为讨论岩溶地表河中等流域尺度无机碳通量的动态变化过程及其影响因素,于2014年1月至12月对漓江流域桂林断面及阳朔断面河水进行为期一个水文年的采样观测,每月定期采样分析。结果表明,这个过程主要受水循环过程控制,除岩溶水化学特征沿途发生变化之外,水体SIc和SId值也逐渐偏正,溶蚀能力逐渐降低,所产生的无机碳通量仍然不断增加,且呈现出旱季低雨季高的特征。通过计算,桂林断面无机碳通量为7.42×107kgCO2·a-1,阳朔断面为27.9×107kgCO2·a-1,其中桂林断面碳酸盐岩风化所产生的无机碳通量和硅酸盐岩风化所产生的无机碳通量分别占总通量的72.67%和5.21%,阳朔断面分别占87.51%和2.89%,表明硅酸盐岩风化的贡献率沿途不断减小,碳酸盐岩风化的贡献率不断增加。桂林断面以上流域碳汇强度为2.69×104kgCO2·km-2·a-1,桂林到阳朔断面流域碳汇强度为9.89×104 kgCO2·km-2·a-1,相差近5倍,除沿途大气降水、支流补给、水生生物可能产生的有机碳埋藏等原因外,外源水补给所形成的混合溶蚀作用对岩溶区无机碳通量的增加起着不可忽视的作用。 相似文献
6.
岩石风化碳汇是全球碳汇的重要组成部分,通过对赤水河流域水体主要离子组成进行测定,分析赤水河流域河水水化学特征及其岩石风化过程对大气CO_2的消耗。结果表明:赤水河流域离子组成以Ca~(2+),Mg~(2+),HCO_3~-和SO_4~(2-)为主,河水总溶解性固体(TDS)含量均值为317.88 mg/L,高于全球流域均值(65 mg/L)。元素比值分析表明赤水河流域离子组成主要受岩石风化控制,其中碳酸盐岩风化为主导控制因素,碳酸盐岩、硅酸盐岩对河水溶质贡献率分别为70.77%和5.03%。人类活动和大气降水对流域河水溶质的贡献很小。流域岩石化学风化速率为126.716 t/(km~2·a),高于黄河、长江、乌江及世界河流均值。流域岩石化学风化对大气CO_2的消耗量为10.96×10~9mol/a,岩石风化对大气CO_2消耗速率为5.79×10~5mol/(km~2·a),与长江流域接近,高于黄河流域。 相似文献
7.
《地质学报》2016,(8)
流域的岩石化学风化过程是全球碳循环中的重要环节。以往的流域水化学碳汇通量估算大多是基于碳酸对岩石的风化作用。而实际上,硫酸和碳酸一样,也参与了碳元素的地球化学循环,从而对全球碳循环过程产生影响。长江流域水体近几年出现酸化现象,大部分河段SO_4~(2-)和Ca~(2+)含量增高,其对应的岩石风化过程和大气CO_2消耗速率也发生变化。文章对长江干流及主要支流2013年不同季节的离子组成进行监测,利用水化学平衡法和Galy估算模型,对长江流域岩石化学风化速率和CO_2消耗通量进行了估算,对硫酸参与下的长江流域岩石风化和碳循环过程进行了分析。结果表明,长江流域水体离子主要来源于硅酸盐岩风化和碳酸盐岩风化。其中碳酸盐岩风化对河水离子贡献率为92%。在硅酸盐岩广泛分布的赣江流域,碳酸盐岩风化离子贡献也达85%。分析表明,硫酸参与了长江流域的岩石风化过程,对水体中离子产生一定影响。硫酸的参与加快了碳酸盐岩的化学风化速率,平均提高约28%。在不考虑硫酸溶蚀作用下,流域大气CO_2消耗速率平均为514.12×10~3 mol/km~2·a,但是硫酸参与时,CO_2消耗速率为467.18×10~3 mol/km~2·a,扣除碳汇量约14%。在各支流中,乌江流域受硫酸影响最大,而对雅砻江的影响最小,这与乌江流域的含煤地层、矿床硫化物及大气酸沉降有关。 相似文献
8.
青藏高原化学风化和对大气CO2的消耗通量 总被引：1，自引：0，他引：1
为了评估青藏高原化学风化对全球气候的影响,笔者等对中国境内源自青藏高原的七条主要河流（金沙江、澜沧江、怒江、黄河、雅砻江、岷江和大渡河）进行了采样和地球化学分析,估算了硅酸盐、碳酸盐风化对河水中主量离子的贡献,以及硅酸盐风化和碳酸盐风化所消耗的大气CO2。研究显示,七条河流流域中硅酸盐风化引起的大气CO2消耗约为0.7×10^5～3.7×10^5mol/（km^2·a）。结合国外学者对于喜马拉雅山南缘三条河流（恒河、布拉马普特拉河和印度河）的研究结果可以得出,发源于喜马拉雅山-青藏高原的主要十条河流流域硅酸盐风化平均共消耗大气CO2328×10^9mol/a,仅占全球大陆硅酸盐岩风化所消耗大气CO28700×10^9mol/a的3.8%,并仅为全球通过河流向海洋输送有机碳（来自陆地上生物的消耗）通量的2.5%。 相似文献
9.
流域的岩石化学风化过程是全球碳循环中的重要环节。近年来流域水化学碳汇通量估算已越来越多地关注到外源水(硅酸盐风化)及外源酸对全球碳循环的影响。文章选取万华岩地下河流域为研究区,流域硅酸盐岩和碳酸盐岩分布面积占比为64%和36%,于2017年对洞口进行为期一年的取样监测,并分别于4月和9月对万华岩地下河系统内13个水点的离子组成进行监测,利用水化学平衡法和Galy模型,对流域岩石化学风化速率和CO2消耗通量进行了计算,对万华岩地下河系统的岩石风化和碳循环过程进行了分析。结果表明,万华岩地下河系统岩石风化消耗CO2的速率为31.02 t·(km2·a)-1;以碳酸岩风化为主,其风化速率为硅酸盐溶蚀的20倍;流域内碳酸盐岩风化对CO2消耗量占到整个流域的92.16%;不同岩石风化类型对碳通量的贡献率以碳酸溶解碳酸盐岩最大,为87.06%;流域上游的外源水对岩溶碳汇具有巨大的促进作用,外源水汇入后碳酸盐岩碳汇速率可以达到无外源水汇入流域的2倍;硫酸溶解碳酸盐岩次之,为9.24%;碳酸风化硅酸盐岩最小,为3.7%,在计算流域碳汇量的时候应将硫酸参与岩石风化的影响去除。 相似文献
10.
秦建华 《沉积与特提斯地质》2008,28(1):1-6
2000-2002年期间,笔者对青藏高原东部长江流域溶质载荷分别进行了取样分析并对流域盆地化学剥蚀通量、剥蚀速率和大气CO2净消耗率进行了计算。结果表明,流域盆地化学剥蚀速率以河源区楚玛尔河最高为2.34×10^6mol/a/km^2,沱沱河最低为1.40×10^6mol/a/km^2,四大支流雅砻江为1.69×10^6mol/a/km^2,金沙江为1.74×10^6mol/a/km^2,大渡河为1.57×10^6mol/a/km^2,岷江为1.88×10^6mol/a/km^2;流域盆地ФCO2估算结果以大渡河最高为101.81×10^3mol/a/km^2,楚玛尔河最低为7.55×10^3mol/a/km^2,金沙江为44.38×10^3mol/a/km^2,雅砻江为69.64×10^3mol/a/km^2,岷江为81.90×10^3mol/a/km^2,沱沱河为21.90×10^3mol/a/km2^。并对长江流域地表化学剥蚀速率主要控制因素进行了讨论。 相似文献
11.
《Applied Geochemistry》1994,9(1):1-13
Data on carbon river fluxes recently obtained by the authors for the Congo basin within the framework of the PIRAT Program (INSU-CNRS/ORSTOM) are compared with results previously obtained for the Amazon basin. A special interest is devoted to the bicarbonate river fluxes and to their relationships with river discharges. The flux of atmospheric and soil CO2 consumed by rock weathering is estimated to be 3.1 × 105 and 0.5 × 105 moles/a/km2 respectively for the Amazon and the Congo basin. These CO2 fluxes represent, respectively, 67.4% and 74.7% of the total bicarbonate river fluxes. A comparison to other large river basins shows that this contribution is directly related to the proportion of carbonate rock areas. A transfer function between the weathering CO2 flux and the river discharge is calculated for each basin and allows the reconstitution of the variations of this flux using the river discharge fluctuations during the last century. These interannual CO2 fluctuations present average increasing trends of 10% for Amazon basin and only 0.7% for the Congo basin during the last century. 相似文献
12.
我国南方岩溶区与北方黄土区都是巨大的碳库。碳酸盐的溶蚀及再结晶是两个碳库与大气ＣＯ２交换的重要过程。碳的区域平衡是评价化学风化消耗或逸散ＣＯ２的基础。岩溶区与黄土区在地球化学风化的环境背景、溶蚀过程、产物运移和归宿等差异很大。黄土区化学风化消耗大气ＣＯ２通量较岩溶区小。目前评价两类地区土壤与大气ＣＯ２的源汇关系尚不成熟,需要定量认识土壤ＣＯ２与下伏碳酸盐岩溶蚀或与下伏黄土次生碳酸盐化作用。岩溶区湖泊沉积物中有机质分解产生的ＨＣＯ３－制约外源及内生碳酸盐溶解和自生碳酸盐形成。 相似文献
13.
为了探讨接触变质带内变碳酸盐岩变质过程CO2释放的数量和排放CO2的物理、化学及地质条件,根据递进变质反应和时间积分流体通量模型,定量分析和定量计算了双山地区变碳酸盐岩在接触变质作用中释放CO2的通量。计算结果得到CO2的通量值为0.729×104~2.446×104 mol/cm2,CO2的来源以接触变质反应释放为主;CO2的生成释放与变质程度呈正相关关系。自白云石带至方解石带变质流体中XCO2不断升高,但钙铝榴石带由于岩浆水影响,流体通量最高而XCO2急剧下降。 相似文献
14.
John M. Ferry Boswell A. Wing Sarah C. Penniston-Dorland Douglas Rumble 《Contributions to Mineralogy and Petrology》2002,142(6):679-699
Periclase formed in siliceous dolomitic marbles during contact metamorphism in the Monzoni and Predazzo aureoles, the Dolomites, northern Italy, by infiltration of the carbonate rocks by chemically reactive, H2O-rich fluids at 500 bar and 565-710 °C. The spatial distribution of periclase and oxygen isotope compositions is consistent with reactive fluid flow that was primarily vertical and upward in both aureoles with time-integrated flux ~5,000 and ~300 mol fluid/cm2 rock in the Monzoni and Predazzo aureoles, respectively. The new results for Monzoni and Predazzo are considered along with published studies of 13 other aureoles to draw general conclusions about the direction, amount, and controls on the geometry of reactive fluid flow during contact metamorphism of siliceous carbonate rocks. Flow in 12 aureoles was primarily vertically upward with and without a horizontal component directed away from the pluton. Fluid flow in two of the other three was primarily horizontal, directed from the pluton into the aureole. The direction of flow in the remaining aureole is uncertain. Earlier suggestions that fluid flow is often horizontal, directed toward the pluton, are likely explained by an erroneous assumption that widespread coexisting mineral reactants and products represent arrested prograde decarbonation reactions. With the exception of three samples from one aureole, time-integrated fluid flux was in the range 102-104 mol/cm2. Both the amount and direction of fluid flow are consistent with hydrodynamic models of contact metamorphism. The orientation of bedding and lithologic contacts appears to be the principal control over whether fluid flow was either primarily vertical or horizontal. Other pre-metamorphic structures, including dikes, faults, fold hinges, and fracture zones, served to channel fluid flow as well. 相似文献
15.
Theodore C. Labotka Lawrence M. Anovitz James G. Blencoe 《Contributions to Mineralogy and Petrology》2002,144(3):305-313
The molar volume of mixtures of CO2 and H2O is a strong function of the fluid composition. Both CO2 and H2O participate in the metamorphism of carbonate rocks, resulting in a change in the fluid composition during reaction. One of the effects of the change in composition is the increase in pore-fluid pressure with only small increases in extent of reaction, ;. Pressure calculated from the volumetric properties of CO2-H2O mixtures at 400 °C increases greatly with small increases of ; but drops at greater values because of the increase in pore volume as a result of (Vsolid. The pore pressure increase at small values of ;, though, readily exceeds the reported tensile strength of carbonate rocks, and the rock cannot sustain significant reaction without fracturing. The result of a small amount of reaction is a fractured rock with increased permeability, which promotes fluid transport. 相似文献
16.
《Geochimica et cosmochimica acta》1999,63(7-8):967-987
The conventional view of the climatic influence on weathering is that weathering rates are strongly temperature-dependent due to the near-exponential relationship (Clausius-Clapeyron) between temperature and the saturation vapor pressure of water, and hence precipitation and runoff. This is a central theme in the Earth “thermostat” model, i.e., weathering of aluminosilicate rocks on continents acts through the greenhouse effect as a negative feedback on atmospheric CO2. However, there is very little direct field evidence to support this hypothesis. To remedy the lack of systematic geochemical data for cold high latitude rivers as compared to the tropics, large, pristine drainages of Eastern Siberia have been studied. Here, data from basement terrains of the Siberian Craton are reported. The low Si to total cation ratios suggest a superficially weathered system. The total dissolved solids flux of 0.39 × 106 mol/km2/yr and the CO2 uptake flux of 149 × 103 mol/km2/yr are similar to those of the tropical cratonic systems and the collisional/accretionary zone of northeastern Siberia, but about a factor of 3 lower than for the orogenic zones of the western Americas at both low and high latitudes. The lack of systematic climatic effects on the solute and CO2 fluxes is ascribed to the unique non-glacial frost shattering processes which continuously expose fresh rock surfaces and, thus, overcome the effect of temperature inhibition on high-latitude shields and to the lateritic cover that seals in the weathering front away from the weathering agents on the tropical shields. No primary climatic effects on weathering rates on the present Earth were detected. 相似文献
17.
安徽歙县伏川的蛇绿岩套形成于中-晚元古宙,其Nd、Sr和O同位素组成是:εNd(T)=+0.7-+3.8,εSr(T)=+30.7-+53.9,δ18O=3.2-11.0‰。据地质学和同位素地球化学特征,该岩套位于杨子板块南缘、江南古岛弧的弧后小洋盆地轴部。εNd(T)值的变化是由于蛇绿岩形成过程中受到下伏不成熟硅铝质基底地壳的混染引起的;εSr(T)和δ18O的变化,是在蛇绿岩形成时或形成后不久遭受海水热液蚀变的结果。 相似文献
18.
Nils Moosdorf Jens Hartmann Benjamin Hagedorn 《Geochimica et cosmochimica acta》2011,75(24):7829-7854
CO2 consumption by chemical weathering is an integral part of the boundless carbon cycle, whose spatial patterns and controlling factors on continental scale are still not fully understood. A dataset of 338 river catchments throughout North America was used to empirically identify predictors of bicarbonate fluxes by chemical weathering and interpret the underlying controlling factors. Detailed analysis of major ion ratios enables distinction of the contributions of silicate and carbonate weathering and thus quantifying CO2 consumption. Extrapolation of the identified empirical model equations to North America allows the analysis of the spatial patterns of the CO2 consumption by chemical weathering.Runoff, lithology and land cover were identified as the major predictors of the riverine bicarbonate fluxes and the associated CO2 consumption. Other influence factors, e.g. temperature, could not be established in the models. Of the distinguished land cover classes, artificial surfaces, dominated by urban areas, increase bicarbonate fluxes most, followed by shrubs, grasslands, managed lands, and forests. The extrapolation results in an average specific bicarbonate flux of 0.3 Mmol km−2 a−1 by chemical weathering in North America, of which 64% originates from atmospheric CO2, and 36% from carbonate mineral dissolution. Chemical weathering in North America thus consumes 50 Mt atmospheric CO2-C per year. About half of that originates from 10% of the area of North America.The estimated strength of individual predictors differs from previous studies. This highlights the need for a globally representative set of regionally calibrated models of CO2 consumption by chemical weathering, which apply very detailed spatial data to resolve the heterogeneity of earth surface processes. 相似文献
19.
A detailed geochemical study on river waters of the Australian Victorian Alps was carried out to determine: (i) the relative significance of silicate, carbonate, evaporite and sulfide weathering in controlling the major ion composition and; (ii) the factors regulating seasonal and spatial variations of CO2 consumption via silicate weathering in the catchments. Major ion chemistry implies that solutes are largely derived from evaporation of precipitation and chemical weathering of carbonate and silicate lithologies. The input of solutes from rock weathering was determined by calculating the contribution of halite dissolution and atmospheric inputs using local rain and snow samples. Despite the lack of carbonate outcrops in the study area and waters being undersaturated with respect to calcite, the dissolution of vein calcite accounts for up to 67% of the total dissolved cations, generating up to 90% of dissolved Ca and 97% of Mg. Dissolved sulfate has δ34S values of 16 to 20‰CDT, indicating that it is derived predominantly from atmospheric deposition and minor gypsum weathering and not from bacterial reduction of FeS2. This militates against sulphuric acid weathering in Victorian rivers. Ratios of Si vs. the atmospheric corrected Na and K concentrations range from ~ 1.1 to ~ 4.3, suggesting incongruent weathering from plagioclase to smectite, kaolinite and gibbsite.Estimated long-term average CO2 fluxes from silicate weathering range from ~ 0.012 × 106 to 0.039 × 106 mol/km2/yr with the highest values in rivers draining the basement outcrops rather than sedimentary rocks. This is about one order of magnitude below the global average which is due to low relief, and the arid climate in that region. Time series measurements show that exposure to lithology, high physical erosion and long water–rock contact times dominate CO2 consumption fluxes via silicate weathering, while variations in water temperature are not overriding parameters controlling chemical weathering. Because the atmospheric corrected concentrations of Na, K and Mg act non-conservative in Victorian rivers the parameterizations of weathering processes, and net CO2 consumption rates in particular, based on major ion abundances, should be treated with skepticism. 相似文献