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1.
以疏勒河源区为研究区,自2018年12月至2019年11月分别采集河水、泉水和雪样样品44个、4个和7个,综合运用Piper三线图、Gibbs图、离子比值法定性分析不同水体水化学特征及控制因素,利用质量平衡法(正向地球化学模型)量化不同来源对不同季节河水水化学成分的贡献率。结果表明:疏勒河源区不同水体水化学特征存在差异,TDS含量为泉水>河水>冰川融水>雪水,河水水化学类型冬季为HCO3--Mg2+?Ca2+型,春季为HCO3--Ca2+?Mg2+?Na+型,夏、秋季均为HCO3--Ca2+?Mg2+型,泉水和雪水分别为HCO3--Ca2+?Mg2+型、HCO3--Ca2+型;受多种因素共同影响,不同季节河水主离子时空变化均存在差异;河水和泉水水化学组成受岩石风化作用控制,主离子来源于以白云石为主的碳酸盐岩风化、硅酸盐岩风化和盐岩、石膏、硫酸盐矿物等蒸发岩溶解;正向地球化学模型计算结果表明冬春季河水阳离子主要来源于硅酸盐岩风化溶解,夏秋季碳酸盐岩对河水阳离子贡献率大于硅酸盐岩,总体河水阳离子主要来源于碳酸盐岩和硅酸盐岩风化。  相似文献   

2.
发源于唐古拉山山脉的河流在青藏高原地区具有流域面积大、径流距离长以及流量大等特点,与喜马拉雅山地区河流共同组成全球河源区最高的水流系统。它们的物理与化学侵蚀在很大程度上代表了在全球气候变化的条件下,大陆的侵蚀作用所发生的变化,即大陆与海洋的物质运移和平衡。发源于唐古拉山北坡的长江源头主要支流楚玛尔河与沱沱河的物理化学特点是溶解的化学成分含量较高,一般为10.66~410.81mmol/L,主要阳离子为Na+、Ca2+和Mg2+,占阳离子总量的97%以上。Ca2+/Na+、Mg2+/Na+、K+/Na+的比值较低,87Sr/86Sr值为(0.708954±0.000020)~(0.711860±0.000011),表明唐古拉山北坡的河水成分以蒸发岩类溶解为主。发源于唐古拉山南坡的怒江源头以及雅鲁藏布江及其支流等的主要阳离子为Ca2+、Mg2+、Na+,占阳离子总量的97%以上。Ca2+/Na+、Mg2+/Na+、K+/Na+的比值较高,87Sr/86Sr值为(0.705534±0.000016)~(0.722856±0.000014),表现为以碳酸盐岩和硅酸盐岩的溶解为主。长江河源区河水中主要化学成分来自蒸发岩,其中Na+和Cl-在河流水化学成分中占比例最大,经计算,唐古拉山北坡长江源头地区的物理侵蚀率为77kg/(km.2a),蒸发岩的化学侵蚀率为49~72.7t/(km.2a),碳酸盐岩的化学侵蚀率为15~20t/(km.2a),硅酸盐岩的化学侵蚀率为2~5t/(km.2a);南坡物理侵蚀率为34kg/(km.2a),碳酸盐岩的化学侵蚀率为25~30t/(km.2a),硅酸盐岩的化学侵蚀率为7~10t/(km.2a)。这些特征反映出北坡高寒干旱环境下河流蒸发岩的化学侵蚀作用较强,南坡碳酸盐岩和硅酸盐岩的化学侵蚀作用大于北坡。  相似文献   

3.
The chemical and isotopic characteristics of the water and suspended particulate materials(SPM) in the Yangtze River were investigated on the samples collected from 25 hydrological monitoring stations in the mainsteam and 13 hydrological monitoring stations in the major tributaries during 2003 to 2007. The water samples show a large variation in both δD( 30‰ to 112‰) and δ18O( 3.8‰ to 15.4‰) values. Both δD and δ18O values show a decrease from the river head to the Jinsha Jiang section and then increase downstream to the river mouth. It is found that the oxygen and hydrogen isotopic compositions of the Yangtze water are controlled by meteoric precipitation, evaporation, ice(and snow) melting and dam building. The Yangtze SPM concentrations show a large variation and are well corresponded to the spatial and temporal changes of flow speed, runoff and SPM supply, which are affected by the slope of the river bed, local precipitation rate, weathering intensity, erosion condition and anthropogenic activity. The Yangtze SPM consists of clay minerals, clastic silicate and carbonate minerals, heavy minerals, iron hydroxide and organic compounds. From the upper to lower reaches, the clay and clastic silicate components in SPM increase gradually, but the carbonate components decrease gradually, which may reflect changes of climate and weathering intensity in the drainage area. Compared to those of the upper crust rocks, the Yangtze SPM has lower contents of SiO2, CaO, K2 O and Na2 O and higher contents of TFe2 O3 and trace metals of Co, Ni, Cu, Zn, Pb and Cd. The ΣREE in the Yangtze SPM is also slightly higher than that of the upper crust. From the upper to lower reaches, the CaO and MgO contents in SPM decrease gradually, but the SiO2 content increases gradually, corresponding to the increase of clay minerals and decrease of the carbonates. The δ30SiSPM values( 1.1‰ to 0.3‰) of the Yangtze SPM are similar to those of the average shale, but lower than those of the granite rocks( 0.3‰ to 0.3‰), reflecting the effect of silicon isotope fractionation in silicate weathering process. The δ30SiSPM values of the Yangtze SPM show a decreasing trend from the upper to the middle and lower reaches, responding to the variation of the clay content. The major anions of the river water are HCO 3, SO 4 2, Cl, NO 3, SiO 4 4 and F and the major cations include Ca2+, Na+, Mg2+, K+ and Sr2+. The good correlation between HCO3-content and the content of Ca2+may suggest that carbonate dissolution is the dominate contributor to the total dissolved solid(TDS) of the Yangtze River. Very good correlations are also found among contents of Cl, SO4 2, Na+, Mg2+, K+and Sr2+, indicating the important contribution of evaporite dissolution to the TDS of the Yangtze River. High TDS contents are generally found in the head water, reflecting a strong effect of evaporation in the Qinghai-Tibet Plateau. A small increase of the TDS is generally observed in the river mouth, indicating the influence of tidal intrusion. The F and NO3 contents show a clear increase trend from the upstream to downstream, reflecting the contribution of pesticides and fertilizers in the Chuan Jiang section and the middle and lower reaches. The DSi shows a decrease trend from the upstream to downstream, reflecting the effect of rice and grass growth along the Chuan Jiang section and the middle and lower reaches. The dissolved Cu, Zn and Cd in the Yangtze water are all higher than those in world large rivers, reflecting the effect of intensive mining activity along the Yangtze drainage area. The Yangtze water generally shows similar REE distribution pattern to the global shale. The δ30SiDiss values of the dissolved silicon vary from 0.5‰ to 3.7‰, which is the highest among those of the rivers studied. The δ30SiDiss values of the water in the Yangtze mainsteam show an increase trend from the upper stream to downstream. Its DSi and δ30SiDiss are influenced by multiple processes, such as weathering process, phytolith growth in plants, evaporation, phytolith dissolution, growth of fresh water diatom, adsorption and desorption of aqueous monosilicic acid on iron oxide, precipitation of silcretes and formation of clays coatings in aquifers, and human activity. The δ34SSO4 values of the Yangtze water range from 1.7‰ to 9.0‰. The SO4 in the Yangtze water are mainly from the SO4 in meteoric water, the dissolved sulfate from evaporite, and oxidation of sulfide in rocks, coal and ore deposits. The sulfate reduction and precipitation process can also affect the sulfur isotope composition of the Yangtze water. The87Sr/86Sr ratios of the Yangtze water range from 0.70823 to 0.71590, with an average value of 0.71084. The87Sr/86Sr ratio and Sr concentration are primary controlled by mixing of various sources with different87Sr/86Sr ratios and Sr contents, including the limestone, evaporite and the silicate rocks. The atmospheric precipitation and anthropogenic inputs can also contribute some Sr to the river. The δ11B values of the dissolved B in the Yangtze water range from 2.0‰ to 18.3‰, which is affected by multifactors, such as silicate weathering, carbonate weathering, evaporite dissolution, atmospheric deposition, and anthropogenic inputs.  相似文献   

4.
青藏高原东部金沙江流域盆地陆地风化特征   总被引:2,自引:0,他引:2       下载免费PDF全文
青藏高原东部金沙江流域是研究高原隆升与陆地风化的理想地区。本文通过对金沙江河流系统的取样,从河流溶质载荷主要离子和悬浮载荷粘土矿物等方面揭示青藏高原东部金沙江流域盆地陆地风化特征。研究表明,金沙江流域盆地陆地岩石风化主要是碳酸盐岩、蒸发盐岩和硅酸盐岩。利用S i、S i/TZ+*、S i/Na*+K和S i/K以及(Na*+K)/TZ+等5个指标结合流域区域岩石分布和土壤特征揭示出流域硅酸盐岩为浅表性初级风化,风化产物主要是富含阳离子的次生粘土矿物。  相似文献   

5.
We investigated the geochemical characteristics of major, trace and rare earth elements and Sr–Nd isotope patterns of bed sediments from the headwaters and upper reaches of the six large rivers draining the Tibetan Plateau (the Jinsha River—Yangtze, Lancang River—Mekong, Nujiang River—Salween, Huang He—Yellow, Indus, and Yarlung Tsangpo—Brahmaputra). By using Ca/Al versus Mg/Al, La/Sc versus Co/Th, and 87Sr/86Sr versus εNd (0) binary differentiation diagrams of provenance, some typical contributors to the different catchment sediments can be identified. In the Three-River (the Jinsha, Lancang, and Nujiang Rivers) tectonomagmatic belt, acidic–intermediate-acidic volcanic rocks are very important provenance of sediments. Carbonate rocks and Permian Emeishan basalts are dominant in the Jinsha River. The Yellow River sediments have similar geochemical characteristics with loess in catchments. The Indus and Yarlung Tsangpo Rivers sediments are mainly from ultra-K volcanic rocks and Cenozoic granitoids widely distributed in the Indus–Yarlung suture. The intensity of chemical weathering in these river catchments is evaluated by calculating the chemical indices of alteration (CIA) of sediments and comparing them with bedrocks. The CIA values of the six river sediments are from 46.5 to 69.6, closing to those of bedrocks in the corresponding catchment, which indicates relatively weak chemical weathering intensity. Lithology, climate, and topography affect the chemical weathering intensity in these river catchments.  相似文献   

6.
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   

7.
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   

8.
红河盆地的化学风化作用:主要和微量元素地球化学记录   总被引:1,自引:0,他引:1  
河流沉积物的元素含量有助于反映其流域的自然风化过程。红河是世界上重要的河流之一,但其沉积物的地球化学研究却几乎没有。本文通过开展红河盆地干流和主要支流40个样品的主要和微量元素地球化学分析,发现红河流域硅酸盐岩的化学风化作用为中等强度,与长江及亚马逊河的风化强度相近,而高于黄河,低于珠江;且化学风化作用受该区域的气候和构造作用控制。  相似文献   

9.
A detailed investigation of the fluvial geochemistry of the Han River system allows to estimate the rates of chemical weathering and the consumption of CO2. The Han River drains approximately 26,000 km2 and is the largest river system in South Korea in terms of both water discharge and total river length. It consists of two major tributaries: the North Han River (NHR) and the South Han River (SHR). Distinct differences in basin lithology (silicate vs. carbonate) between the NHR and SHR provide a good natural laboratory in which to examine weathering processes and the influence of basin geology on water quality. The concentrations of major elements and the Sr isotopic compositions were obtained from 58 samples collected in both summer and winter along the Han River system in both 2000 and 2006. The concentrations of dissolved loads differed considerably between the NHR and SHR; compared with the SHR, the NHR had much lower total dissolved solids (TDS), Sr, and major ion concentrations but a higher Si concentration and 87Sr/86Sr ratio. A forward model showed that the dissolved loads in the NHR came primarily from silicate weathering (55 ± 11%), with a relatively small portion from carbonates (30 ± 14%), whereas the main contribution to the dissolved loads in the SHR was carbonate weathering (82 ± 3%), with only 11 ± 4% from silicates. These results are consistent with the different lithologies of the two drainage basins: silicate rocks in the NHR versus carbonate rocks in the SHR. Sulfuric acid derived from sulfide dissolution in coal-containing sedimentary strata has played an important role in carbonate weathering in the SHR basin, unlike in the NHR basin. The silicate weathering rate (SWR) was similar between the NHR and SHR basins, but the rate of CO2 consumption in the SHR basin was lower than in the NHR basin due to an important role of sulfuric acid derived from pyrite oxidation.  相似文献   

10.
本文根据2013年10月至2015年4月桂江桂林站的采样分析数据,讨论桂江上游的水化学组成及河水离子的主要来源。结果表明,研究区河水水化学类型为HCO3-Ca型,HCO3-和Ca2+是主要的阴阳离子,主要来源于流域内碳酸对碳酸盐岩的风化溶解,河水主要离子浓度受流量变化的影响,呈现出冬高夏低的趋势。同时,流域内硫酸也参与了碳酸盐岩的风化。此外,虽然流域内碳酸盐岩仅少量分布,但河水水化学特征仍受碳酸盐岩和硅酸盐岩的共同控制。主成分分析结果表明,第一因子贡献率为38.8%,与K+、Na+、Mg2+、Cl-、SO42-、NO3-相关性较大,在本研究中代表人类活动及大气沉降的影响,其中NO3-主要来源于流域内农业活动的面源污染;第二因子贡献率为28.2%,与HCO3-和Ca2+相关性大,代表碳酸盐岩的溶解;第三因子没有明显具有高载荷的指标。   相似文献   

11.
长江流域面积巨大,岩性多变,加之三峡大坝等重大水利工程的影响,干流河水的水化学成因存在较大争议。此外,以往研究中流域矿物风化过程的碳汇通量估算一般基于阳离子来源分析,但该算法通常涉及多种矿物端元的参数选取,结果具有不确定性。本次研究对长江干流水化学的时空演变进行了整体分析,并基于上游河水样品HCO3~-含量的校正与计算,提出了一种计算矿物风化过程碳汇通量的新方法。研究结果表明,蒸发盐溶解、循环盐作用、矿物风化及硫酸盐溶解是控制长江干流河水离子组成的主要水文地球化学作用,而人类活动主要影响了离海距离3 000 km以内河水NO3~-含量;长江上游干流硅酸盐风化消耗CO2速率为1.16×10~5 mol/(km~2·a),碳酸盐风化消耗CO2速率为4.75×10~5 mol/(km~2·a)。本研究有助于加深对长江干流主要水文地球化学作用的认识,丰富和完善碳循环研究理论。  相似文献   

12.
本文主要描述和讨论了四川省攀枝花市沿金沙江分布、并以炳草岗地龙箐剖面为代表的昔格达组湖相沉积下伏的砾石层的沉积特征及其河流相成因.根据前人对昔格达组湖相沉积的磁性地层学研究结果,为4.2/3.28~2.6/2.12/1.78 MaBP的上新世中、晚期或至早更新世早期,表明其下伏厚达50 m的砾石层的形成时代约为4.2~4.5/5 MaBP的上新世早期.早上新世金沙江河流相砾石层在接近金沙江谷底位置的发现,表明金沙江很早就已经从青藏高原主夷平面下切了2000 m以上、已在接近其现今谷底的位置上存在.这对于探讨古金沙江的河谷发育及其与青藏高原隆升的关系,具有重要的指示意义.  相似文献   

13.
为深入评估中国南方陆地风化过程及河流物质循环过程, 通过测定西江主要干、支流丰水期及枯水期水体主要离子和锶及其同位素比值, 结合Galy模型对西江流域化学风化特征及CO2消耗通量进行计算。结果表明: (1)西江流域化学风化受人类活动的影响较小, 流域化学风化过程主要受到碳酸的控制。(2)河水阳离子的主要物质来源为硅酸盐岩和碳酸盐岩风化, 硅酸盐岩在丰水期和枯水期的阳离子物质来源摩尔占比均为0.04, 碳酸盐岩中石灰岩占比分别为0.79和0.78, 白云岩分别为0.17和0.18。(3)西江流域在丰水期和枯水期的化学风化过程具有一定的差异性, 由于硫酸参与白云岩的风化作用影响碳酸盐岩风化过程中的CO2消耗通量, 导致各个化学风化过程所涉及的CO2通量有所差别。(4)碳酸风化碳酸盐岩在丰水期和枯水期所消耗的CO2通量分别为(0.78~244.25)×106 mol/km2/yr和(0.10~49.16)×106 mol/km2/yr, 硫酸风化碳酸盐岩所产生的CO2通量分别为(0.25~42.16)×106 mol/km2/yr和(0.01~13.90)×106 mol/km2/yr, 碳酸风化硅酸盐岩所消耗CO2通量的分别为(0.05~17.83)×106 mol/km2/yr和(0.02~6.07)×106 mol/km2/yr。  相似文献   

14.
We collected riverbed sediments of the headwaters of the Yangtze River (Chumaer River, Tuotuo River, Gaerqu River and Buqu River), Tongtian River and Jinsha River (HTJR) flowing on the eastern Tibetan Plateau and analyzed their mineralogical features, major and trace element contents. The results show: (i) very poor correlations of Na2O, K2O, CaO, Ba, and Sr to SiO2, LREE to Th, HREE to Hf, and Ta/La to Ti, and characteristics of Eu anomaly (the ratios of (Eu/Eu*)N range from 0.60 to 0.83 with an average value of 0.71) all indicate that the Jinsha River sediments have not undergone much mineralogical sorting; (ii) illite and chlorite are predominant clay minerals, and quartz, calcite, dolomite, albite, and K-feldspar are prevailing non-clay minerals. The characteristics of mineral assemblage indicate relatively weak chemical weathering degree in these river basins; (iii) very high contents of Fe2O3, MgO, TiO2, Sc, V, Cr, Co, and Ni at Panzhihua mainly result from the huge-sized V–Ti magnetite deposits occurred in layered gabbroic intrusion; and (iv) the chemical alteration index (CIA) in the HTJR ranges from 46.5 to 69.2 and with an average value of 60.5 which indicates relatively weak weathering degree.  相似文献   

15.
The main scope of this study is to investigate parameters controlling chemical weathering rates for a large river system submitted to subarctic climate. More than 110 river water samples from the Mackenzie River system (northern Canada) have been sampled and analyzed for major and trace elements and Sr isotopic ratios in the dissolved phase. The three main morphological units are reflected in water chemistry. Rivers from the Canadian Shield are very dilute, dominated by silicate weathering (Millot et al., 2002), whereas the rivers of the Rocky and Mackenzie Mountains as well as the rivers of the sedimentary Interior Platform are dominated by carbonate weathering and are SO4 rich. Compared to the rivers of the Mackenzie and Rocky Mountains, the rivers of the interior plains are organic, silica, and Na rich and constitute the dominant input term to the Mackenzie River mainstream. Rivers of the Canadian Shield area do not significantly contribute to the Mackenzie River system. Using elemental ratios and Sr isotopic ratios, a mathematical inversion procedure is presented that distinguishes between solutes derived from silicate weathering and solutes derived from carbonate weathering. Carbonate weathering rates are mostly controlled by runoff, which is higher in the mountainous part of the Mackenzie basin. These rates are comparable to the carbonate weathering rates of warmer areas of the world. It is possible that part of the carbonate weathering is controlled by sulfide oxidative weathering, but its extent remains difficult to assess. Conversely to what was stated by Edmond and Huh (1997), overall silicate weathering rates in the Mackenzie basin are low, ranging from 0.13 to 4.3 tons/km2/yr (Na + K + Ca + Mg), and confirm the negative action of temperature on silicate weathering rates for river basins in cold climates. In contrast to what has been observed in other large river systems such as the Amazon and Ganges Rivers, silicate weathering rates appear 3 to 4 times more elevated in the plains than in the mountainous headwaters. This contradicts the “Raymo hypothesis” (Raymo and Ruddiman, 1992). Isotopic characterization of suspended material clearly shows that the higher weathering rates reported for the plains are not due to the weathering of fine sediments produced in the mountains (e.g., by glaciers) and deposited in the plains. Rather, the relatively high chemical denudation rates in the plains are attributed to lithology (uncompacted shales), high mechanical denudation, and the abundance of soil organic matter derived from incomplete degradation and promoting crystal lattice degradation by element complexation. The three- to fourfold factor of chemical weathering enhancement between the plains and mountains is similar to the fourfold factor of enhancement found by Moulton et al. (2000) between unvegetated and vegetated watershed. This study confirms the negative action of temperature on silicate weathering for cold climate but shows that additional factors, such as organic matter, associated with northern watersheds are able to counteract the effect of temperature. This acceleration by a factor of 4 in the plains is equivalent to a 6°C increase in temperature.  相似文献   

16.
认识干旱区地下咸水的形成机制对水资源管理和规划具有重要意义。在宁夏清水河平原上游采集52组浅层地下水化学样品和8组易溶盐样品,分析了地下水咸化的水文地球化学作用,利用元素质量平衡法计算了各作用对地下水盐分的贡献比率。结果表明:沿径流方向,地下水咸化程度呈增加趋势。咸化作用主要为岩石风化,并具空间分异,在补给区以碳酸盐风化为主,在强径流区硫酸盐风化占优,在弱径流区硫酸盐和岩盐风化共同提供了68%~93%的盐量。随着地下水TDS增加,蒸发岩贡献比率上升,碳酸盐和硅酸盐贡献比率下降。蒸发岩风化是导致浅层地下水咸化的首要因素。  相似文献   

17.
Chemical weathering is an integral part of the earth surface processes, whose spatial patterns and controlling factors on continental scale are still not fully understood. Highlands of the Asian continent have been shown having some of the highest observed rates of chemical weathering yet reported. However, the paucity of river gauge data in many of these terrains has limited determination of chemical weathering budget in a continental scale. A dataset of three large watersheds throughout northern Xinjiang in Central Asia is used to empirically identify chemical weathering regimes and interpret the underlying controlling factors. Detailed analysis of major ion ratios and a forward model of mass budget procedure are presented to distinguish the relative significances and contributions of silicate, carbonate weathering and evaporite dissolution. The analytical results show that carbonic acid is the most important weathering agent to the studied watersheds. Silicate weathering contributes, on average, ∼17.8% (molar basis) of total cations on a basin wide scale with an order of Zhungarer > Erlqis > Yili, indicating that silicate weathering, however, does not seem to be intense in the study basins. Evaporite dissolution, carbonate weathering and precipitation input contribute 43.6%, 29.7% and 8.9% of the total dissolved cations on average for the whole catchment, respectively. The three main morphological and hydrological units are reflected in water chemistry. Rivers from the montane areas (recharge area) of the three watersheds are very dilute, dominated by carbonate and silicate weathering, whereas the rivers of piedmont areas as well as the rivers of the sedimentary platform (runoff area) are dominated by carbonate weathering, and rivers of desert plain in the central Zhungarer basin (discharge area) are dominated by evaporite dissolution and are SO4 rich. This spatial pattern indicates that, beside lithology, runoff conditions have significant role on the regional chemical weathering regimes. Chemical weathering processes in the areas appear to be significantly climate controlled, displaying a tight correlation with runoff and aridity. Carbonate weathering are mostly influenced by runoff, which is higher in the mountainous part of the studied basins. The identification of chemical weathering regimes from our study confirmed the weathering potential and complexity of temperate watersheds in arid environment and that additional studies of these terrains are warranted. However, because the dominant weathering reactions in the sedimentary platform of northern Xinjiang are of carbonates and evaporites rather than silicate minerals, and the climatic factors have important role on the rock weathering regimes, we think that weathering at the arid temperate drainage system (Central Asia) is maybe not an important long-term sink for atmospheric CO2, if the future climate has no great change.  相似文献   

18.
The Hanjiang River, the largest tributaries of the Changjiang (Yangtze) River, is the water source area of the Middle Route of China’s South-to-North Water Transfer Project. The chemical and strontium isotopic compositions of the river waters are determined with the main purpose of understanding the contribution of chemical weathering processes and anthropogenic inputs on river solutes, as well as the associated CO2 consumption in the carbonate-dominated basin. The major ion compositions of the Hanjiang River waters are characterized by the dominance of Ca2+ and HCO3 , followed by Mg2+ and SO4 2−. The increase in TDS and major anions (Cl, NO3 , and SO4 2−) concentrations from upstream to downstream is ascribed to both extensive influences from agriculture and domestic activities over the Hanjiang basin. The chemical and Sr isotopic analyses indicate that three major weathering sources (dolomite, limestone, and silicates) contribute to the total dissolved loads. The contributions of the different end-members to the dissolved load are calculated with the mass balance approach. The calculated results show that the dissolved load is dominated by carbonates weathering, the contribution of which accounts for about 79.4% for the Hanjiang River. The silicate weathering and anthropogenic contributions are approximately 12.3 and 6.87%, respectively. The total TDS fluxes from chemical weathering calculated for the water source area (the upper Hanjiang basin) and the whole Hanjiang basin are approximately 3.8 × 106 and 6.1 × 106 ton/year, respectively. The total chemical weathering (carbonate and silicate) rate for the Hanjiang basin is approximately 38.5 ton/km2/year or 18.6 mm/k year, which is higher than global mean values. The fluxes of CO2 consumption by carbonate and silicate weathering are estimated to be 56.4 × 109 and 12.9 × 109 mol/year, respectively.  相似文献   

19.
大河流域的发育史和演化在地学界广受关注。探讨宜宾地区第四纪沉积物中铁质重矿物的特征,可为长江流域的演化提供重要证据,同时对于了解青藏高原东缘的隆升及沉积响应具有重要意义。本文以金沙江和岷江交汇处的宜宾地区第四纪沉积物中的铁质重矿物为研究对象,分析其在电子探针和背散射图像中的化学和形貌学特征,探究长江及其支流的物源演化过程。研究结果显示:岷江下游Ⅴ级阶地至Ⅳ级阶地沉积以磁铁矿为主,物源主要来自龙门山构造带;Ⅲ级阶地沉积以钛铁矿为主,物源仍然主要来自龙门山构造带;现代沉积中蓝晶石、磷灰石等包裹体的铁质矿物增多,其物源来自龙门山构造带和松潘—甘孜褶皱带。岷江Ⅴ级至Ⅲ级阶地形成时,岷江的源头主要位于龙门山构造带;Ⅲ级阶地形成以后,岷江不断向上溯源侵蚀,深入松潘—甘孜褶皱带内,逐渐形成现代岷江。金沙江Ⅴ级阶地和长江Ⅴ级阶地中均未出现攀枝花钒钛磁铁矿,此时金沙江攀枝花—宜宾河段未贯通,长江此时在研究区的物源主要由发源于龙门山构造带的岷江提供。金沙江Ⅳ级阶地中攀枝花钒钛磁铁矿大量出现,表明此时金沙江攀枝花—宜宾河段已经贯通,时间为Ⅳ级阶地开始沉积的时间,即0.5~0.3 Ma BP。  相似文献   

20.
为了掌握亚热带季风气候岩溶地区流域水化学变化特征及量化流域内岩石化学风化过程对吸收大气CO2的贡献,文章选取湘西峒河流域作为研究对象,于2016年7—8月对研究区干流和7个子流域进行了水样采集与分析。结果表明:河水pH平均值为8.31,总体呈偏碱性。EC与TDS的变化范围较大,这主要与流域内岩性的分布有关。水中离子以Ca2+、HCO-3为主,水化学类型为HCO3—Ca型,岩性控制水化学的组成。HCO-3、Ca2+和Mg2+主要来源于碳酸盐岩的风化,其余离子来源多受人为活动影响。峒河流域干流的主要离子中,HCO-3、Ca2+和Mg2+浓度从上游至下游总体下降,反映了河流从碳酸盐岩区流向碎屑岩为主地层的过程。NO-3、K+、Na+、F-、Cl-和SO2-4呈增长趋势,说明峒河受人为污染影响较大,反映出人为活动的密集程度。通过子流域的划分可知流域上游主要受灰岩以及白云岩控制,中游以灰岩控制为主,下游受砂岩、泥岩及碎屑岩控制为主。收集流域最终出口吉首观测站一个水文年的数据并运用水化学—径流法估算出峒河流域无机碳通量为60 477.33 tCO2/a,碳汇强度为71.15 tCO2/(km2·a)。  相似文献   

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