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1.
The authors investigated the effect of Bacillus mucilaginosus on weathering of phosphorite. Analysis of different proteins was of significance in exploring the molecular biological mechanism in the bacterial weathering process. The concrete methods are described as follows: Mineral powder was put into liquid culture medium and B. mucilaginosus was incubated in the medium. The control (group) had no mineral powder in the medium. The treatments and controls were cultured simultaneously under the same condition. In a few days, the supernatant was filtrated, the main cations (Ca^2+, Mg^2+, Na^+, Mn^2+, Al^3+, Fe^3+, K^+) were measured by ICP-OES, and the contents of water soluble phosphorus (Pws) and silicon (Siws) were determined by colorimetry. The residual solid was weighed on the filter paper, followed by digestion with concentrated HNO3. The concentrations of the main cations and Pws, Siws in the digest liquid were measured by using the method mentioned above. After the supernatant was centrifuged, the precipitation was used to analyze the protein differences between the treatment groups and the control groups by 2-dimentional gel electrophoresis (2-DE). The experimental results showed that apatite and quartz were partially weathered, but kaolinite was dissolved completely. The population of bacteria increased when mineral powder was added in the liquid medium. Software analysis and comparison of the 2-DE pictures of bacterial proteins revealed 1134 visible protein spots in the treatment group, and 729 visible protein spots in the control group. To compare the bacterial protein expression contents of the treatment group with those of the control group, there were 496 different protein spots, including 214 protein spots which indicated that the protein contents increased, 75 protein spots were indicative of a decrease, and 207 proteins were newly synthesized. It is proposed that the increased bacterial contents may be related to some protein expression and activation after the  相似文献   

2.
Weathering mechanism of phosphorite rock by Aspergillus niger has been studied. Ten strains of phosphate-solubilizing fungi were isolated from rhizosphere soils by using dilute plate method in solid inorganic phosphorus culture. According to the size of soluble phosphate circle in the medium, a strain of stronger phosphate-solubilizing fungus was acquired, which was identified as, Aspergillus niger using identification methods of morphology and ITS sequences comparison in Genbank. In liquid culture, incubation in static state, the weathering of apatite rock with the fungus by contrast method: putting apatite powder (200 mesh) in liquid culture medium of flask, inoculation fungus after autoclave (setting sterile control) for studying direct weathering process; putting dialysis bag with apatite powder (200 mesh) in liquid culture medium of flask, inoculation fungus after autoclave (setting sterile control) for studying indirect weathering process.  相似文献   

3.
On the basis of the mechanism of formation of mineral inclusions, it may be assumed that a certain relation exists between the compositions of fluid inclusions in various minerals formed at the same stage of hydrothermal activity. In order to study the genetic relationships between different minerals in the Bayan Obo iron deposit, the compositions(K~+, Na~+, Ca~+, Mg~+, F~+, Cl~+, CO_2~(2-), ΣSO_4~(2-) and pH) of inclusions in fluorite(23), hematite(13), magnetite(3), sodium pyroxene(2) and dolomite(5) from the main mine and the eastern mine were determined by using the vacuum decrepitation and leaching methods, and cluster analyses of the data on the compostions were made. The Q-mode cluster analysis indicates that some iron oxide minerals in the deposit are related to dolomite of sedimentary origin, while others are related to fluorite and sodium pyroxene--products of hydrothermal activity. The R-mode cluster analysis shows that the components of the leaching solution may be divided into two groups: one includes CO_2~(2-), Mg~(2+) and H~+(pH), which are obviously associated with dolomite; the other comprises Na~+, K~+, Ca~+, F~+, Cl~+ and SO_4~(2-), which may possibly represent the composition of hydrothermal solutions.The reaction of the Na-F-Cl solution(pH 4.72) with hematite dolomite at 300℃ and 5 × 10~7 Pa and under alternately"static and dynamic" conditions produced large amounts of hematite and fluorite and small amounts of smectite and Na(Fe) silicates, and the hematite-fluorite assemblage accords with the actual geological conditions in the deposit. From a comparison between the compositions of"static" and"dynamic" solution samples, it may be known that the flow reaction facilitates the migration of Fe, F, Ca and other components as well as Na-metasomatism(Na and Si are fixed in a solid phase).The study of the compositions of mineral inclusions and simulation experiments on hydrothermal metasomatism have provided new evidence for the hypothesis of metamorphosed-sedimentary and hydrothermal-remoulding origin of the Bayan Obo deposit, and pointed out emphatically that hydrothermal metasomatism plays an important role in the formation of the mineral deposit, particularly in the main and the east mine.  相似文献   

4.
Bacillus mucilaginosus is a common soil bacterium,and usually used as a model bacterium in studying microbe-mineral interactions.Several reaction mechanisms of B.mucilaginosus weathering silicate minerals were proposed.However,the molecule mechanisms and detailed processes were still unclear.In this paper,bacterium-mineral interactions were studied in terms of variations in pH value over the experimental period,variations in mineral composition,weathering rates of silicate minerals and volatile metabolites in the culture medium,etc.,to further explore the bacterium-mineral interaction mechanisms.The results showed that B.mucilaginosus could enhance silicate mineral weathering obviously.The weathering rates were quite different for various kinds of silicate minerals,and the weathering rate of weathered adamellite could reach 150 mg/m2/d.Although B.mucilaginosus produced little acidic substance,pH in the microenvironment of bacterium-mineral complex might be far lower than that of the circumjacent environment;a large amount of acetic acid was found in the metabolites,and was likely to play an important role as a ligand.These results appear to suggest that acidolysis and ligand degradation are the main mechanisms of B.mucilaginosus dissolving silicate minerals,the formation of bacterium-mineral complexes is the necessary condition for the bacteria weathering silicate minerals,and extracelluar polysaccharides played important roles in bacterium-mineral interaction processes by forming bacterium-mineral complexes and maintaining the spe-cial physicochemical properties of microenvironment.  相似文献   

5.
The behaviour of the rare-earth elements(REE)during the weathering of granites was studied in southern Guangxi,China.Based on the study of the weathering profiles,the soil,weathered and sub-weatereb zones are identified with different REE geochemical behaviours throug the weathering profiles of granite.The Ce anomalies of the weathering profiles cover a large range of values with most falling between 1.02 and 1.43in the soil zone and 0.16and 0.40in the weathered and sub-weathered zones.Light rare-earth elements(LREE) and heavy rare-earth elements(HREE)are enriched to varying degree in the weathering profiles as compared to host granites.In the soil zone,more HREEs are leached than LREEs,and HREEs are more enriched than LREE in the weathered and sub-weathered zones.It is considered that infiltration and adsorption on clays are two processes controlling the enrichment and formation of REE deposits in the weathering profiles of granite.  相似文献   

6.
34samples of loess-paleosol from the Luochuan and Xifeng sections in the Loess Plateau,northern China were eparated into sand,silt and clay fractions and analyzed for their mineral compositions.The results indicate that there is almost no difference between loess and paleosol in mineral composition.Major mineral species are quartz,mica,feldspar and chlorite,accounting for about 88-92% of the total;other minerals are kandite,smectite,vermiculite and a few heavy minerals.The calcite,magnetite and hematite were not taken into consideration because of their removal in the process of sample preparation.The main difference with respect to the mineral composition of samples collected from different sections and different statigraphic levels lies in the amount and grain size of minerals hosted.Comparisons between the Luochuan section and the Xifeng section,between paleosol and loess and between the upper part and the lower part of some paleosol layers show that the formers contain less feldspar but more mica and vermiculite and are finer in grain size,indicating the co-occurrence of both biochemical weathering process responsible for mineral change and physical weathering process leading to grain-size change during the soil-forming processes.This result favours such an explanation of the soil-forming mechanism that loess deposition and paleosol development occurred synchronously,though the rate of soil formation was greater than that of loess deposition,thus leading to soil development.  相似文献   

7.
The F-rich granites in South CHina could be distinguished as the high-P subtype and the low-P subtype according to their P2O5 contents.There are obvious differences in chemical composition of these two subtypes,The high-P subtype is strongly peraluminous and characterized by low silica and very low REE contents,while the low-P subtype is weakly peraluminous and characterized by high silica and very high REE contents.There are also some differences in chmical compositions of feldspars and micas for these two subtypes,The phosphorus of the high-P subtype mainly appears to be in the feldspar structure as PAlSi-2 substitution or subordinately in amblygonite as an accessory mineral,while the phosphorus of the low-P subtype is mainly in apatite and other phosphate minerals.  相似文献   

8.
The mantle xenoliths in the Quaternary ChangbaishanVolcano in southern Jilin Province contain spinel-facies lherzolites. The equilibration temperatures for these samples range from 902oC to 1064oC based on the two-pyroxene thermometer of Brey and K?hler (1990), and using the oxybarometry of Nell and Wood (1991), the oxidation state was estimated from FMQ-1.32 to -0.38 with an average value of FMQ-0.81 (n?=?8), which is comparable to that of abyssal peridotites and the asthenospheric mantle. The fO2 values of peridotites, together with their bulk rock compositions (e.g., Mg#, Al2O3, CaO, Ni, Co, Cr) and mineral compositions (e.g., Mg# of olivine and pyroxene, Cr# [=Cr/[Cr+Al]] and Mg# [=Mg/[Mg+Fe2+] of spinel), suggest that the present-day subcontinental lithospheric mantle (SCLM) beneath the Changbaishan Volcano most likely formed from an upwelling asthenosphere at some time after the late Mesozoic and has undergone a low degree of partial melting. The studied lherzolite xenoliths show low concentrations of S, Cu, and platinum group elements (PGE), which plot a flat pattern on primitive-mantle normalized diagram. Very low concentrations in our samples suggest that PGEs occur as alloys or hosted by silicate and oxide minerals. The compositions of the studied samples are similar to those of peridotite xenoliths in the Longgang volcanic field (LVF) in their mineralogy and bulk rock compositions including the abundance of chalcophile and siderophile elements. However, they are distinctly different from those of peridotite xenoliths in other areas of the North China Craton (NCC) in terms of Cu, S and PGE. Our data suggest that the SCLM underlying the northeastern part of the NCC may represent a distinct unit of the newly formed lithospheric mantle.  相似文献   

9.
The Changkeng gold-silver deposits consist of a sediment-hosted, disseminated gold deposit and a replacement-type silver deposit. The mineralizations of gold and silver are zoned and closely related to the silicification of carbonate and clastic rocks, so that siliceous ores dominate in the deposit. The mineralizing temperature ranges mainly from 300 to 170℃, and K+, Na+, Ca2+, Mg2+, and Cl- are the major ions in the ore-forming fluid. Calculations of distribution of metal complexes show that gold is mainly transported by hydrosulphide complexes, but chloride complexes of silver, iron, lead, and zinc, which are transformed into hydroxyl and hydrosulphide complexes under neutral to weak-alkaline circumstances in the late stage, predominate in the ore-forming solutions. Water-rock interaction is confirmed to be the effective mechanism for the formation of silver ores by computer modelling of reaction of hydrothermal solution with carbonate rocks. The solubility analyses demonstrate that the precipitation  相似文献   

10.
The Campanian-Maastrichtian phosphatic deposits in Egypt,called the Duwi Forma-tion,comprise a part of the extensive Middle East to North African phosphogenic province of Late Cretaceous to Paleogene age.The province holds the greatest accumulation of phosphorites in the geological history,possibly in excess of 70 billion metric tons.The phosphate resources in Egypt alone exceed 3 billion metric tons.Two-third of these three billions occur only in the Abu-Tartur area.Among the phosphorite deposits in Egypt,the phosphorites of the Abu-Tartur area are characterized by high contents of iron ranging from 3% to 7% with an average of 5%.The detailed mineralogical and geochemical studies on the Abu-Tartur phosphorites revealed that iron is found in the form of pyrite,ankerite,clay minerals,microinclusions,and iron oxide.Pyrite,which is the major fraction,occurs as filling cement and partial to complete teplacement of phosphatic grains and confined to the fresh phosphorites while iron oxide occurs as cryp-tocrystalline aggregates of red to brown particles and is confined to the weathered outcrops.Ex-clusive relations between pyrite in the fresh phosphorite samples inside the Abu-Tartur mine and iron oxide in the equivalent horizon of the weathered exposure indicated that iron oxide was formed by the oxidation of pyrite as a result of weathering.All of these forms harm the quality of ore,manufacturing processes,and the produced phosphoric acid and fertilizers.  相似文献   

11.
Geochemistry of soil, soil water, and soil gas was characterized in representative soil profiles of three Michigan watersheds. Because of differences in source regions, parent materials in the Upper Peninsula of Michigan (the Tahquamenon watershed) contain only silicates, while those in the Lower Peninsula (the Cheboygan and the Huron watersheds) have significant mixtures of silicate and carbonate minerals. These differences in soil mineralogy and climate conditions permit us to examine controls on carbonate and silicate mineral weathering rates and to better define the importance of silicate versus carbonate dissolution in the early stage of soil-water cation acquisition.Soil waters of the Tahquamenon watershed are the most dilute; solutes reflect amphibole and plagioclase dissolution along with significant contributions from atmospheric precipitation sources. Soil waters in the Cheboygan and the Huron watersheds begin their evolution as relatively dilute solutions dominated by silicate weathering in shallow carbonate-free soil horizons. Here, silicate dissolution is rapid and reaction rates dominantly are controlled by mineral abundances. In the deeper soil horizons, silicate dissolution slows down and soil-water chemistry is dominated by calcite and dolomite weathering, where solutions reach equilibrium with carbonate minerals within the soil profile. Thus, carbonate weathering intensities are dominantly controlled by annual precipitation, temperature and soil pCO2. Results of a conceptual model support these field observations, implying that dolomite and calcite are dissolving at a similar rate, and further dissolution of more soluble dolomite after calcite equilibrium produces higher dissolved inorganic carbon concentrations and a Mg2+/Ca2+ ratio of 0.4.Mass balance calculations show that overall, silicate minerals and atmospheric inputs generally contribute <10% of Ca2+ and Mg2+ in natural waters. Dolomite dissolution appears to be a major process, rivaling calcite dissolution as a control on divalent cation and inorganic carbon contents of soil waters. Furthermore, the fraction of Mg2+ derived from silicate mineral weathering is much smaller than most of the values previously estimated from riverine chemistry.  相似文献   

12.
Groundwater sampling was accomplished in the basaltic sequence of the Rh?n mountain range, Germany, in order to investigate hydrochemical groundwater evolution and to delineate mineral alteration reactions involved in natural weathering. The hydrochemical compositions of near-surface groundwaters indicate a Ca/Mg–HCO3 type with near-neutral pH and evolve to a Na–HCO3 type with high pH at greater depth. Column experiments were performed with basaltic and phonolitic rock samples to determine individual mineral alteration reactions. The basic reactions could be related to the alteration of olivine, Ca-pyroxene, plagioclase, pyrrhotite, and feldspathoids under formation of secondary clay minerals (smectites, illite) and goethite. The mineral alteration reactions deduced from the leaching experiments by inverse modelling were found to be consistent with the mineral reactions associated with the natural groundwaters. The reactions calculated for groundwater evolution involve the alteration of primary and secondary minerals to produce low-T mineral phase. The conversion of secondary Na-beidellite to illite occurs at a later stage of groundwater evolution, reducing the concentrations of K+ and Mg2+. Near-surface groundwaters do not indicate significant cation exchange. Initial cation exchange requires elevated pH values, with Mg2+ removed from solution preferred to Ca2+. Na-alkalisation of the groundwaters at greater depth suggests the exchange of Na+ for Mg2+ and Ca2+ on Na-beidellite, supported by cation exchange on coatings of iron hydroxides as alteration products. Among the mature high-pH groundwater at greater depth, the dissolution of anorthite and albite has significant effect on groundwater composition.  相似文献   

13.
The relative contributions of dolomite to calcite weathering related to riverine fluxes are investigated on a highly resolved spatial scale in the diverse watersheds of Slovenia, which previous work has shown have some of the highest carbonate-weathering intensities in the world and suggests that dolomite weathering is favored over limestone weathering in mixed carbonate watersheds. The forested Sava and So?a River watersheds of Slovenia with their headwaters in the Julian Alps drain alpine regions with thin soils (<30 cm) and dinaric karst regions with thicker soils (0 to greater than 70 cm) all developed over bedded Mesozoic carbonates (limestone and dolomite), and siliclastic sediments is the ideal location for examining temperate zone carbonate weathering. This study extends previous work, presenting geochemical data on source springs and documenting downstream geochemical fluctuations within tributaries of the Sava and So?a Rivers. More refined sampling strategies of springs and discrete drainages permit directly linking the stream Mg2+/Ca2+ ratios to the local bedrock lithology and the HCO3 ? concentrations to the relative soil depths of the tributary drainages. Due to differences in carbonate source lithologies of springs and tributary streams, calcite and dolomite weathering end members can be identified. The Mg2+/Ca2+ ratio of the main channel of the Sava River indicates that the HCO3 ? concentration can be attributed to nearly equal proportions by mass of dolomite relative to calcite mineral weathering (e.g., Mg2+/Ca2+ mole ratio of 0.33). The HCO3 ? concentration and pCO2 values increase as soil thickness and alluvium increase for discrete spring samples, which are near equilibrium with respect to calcite. Typically, this results in approximately 1.5 meq/l increase in HCO3 ? from the alpine to the dinaric karst regions. Streams in general do not change in HCO3 ?, Mg2+/Ca2+, or Mg2+/HCO3 ? concentrations down course, but warming and degassing of CO2 produce high degrees of supersaturation with respect to calcite. Carbonate-weathering intensity (mmol/km2-s) is highest within the alpine regions where stream discharge values range widely to extreme values during spring snowmelt. Overall, the elemental fluxes of HCO3 ?, Ca2+, and Mg2+ from the tributary watersheds are proportional to the total water flux because carbonates dissolve rapidly to near equilibrium. Importantly, dolomite weathers preferentially over calcite except for pure limestone catchments.  相似文献   

14.
Major ions showed high concentrations, ionic strength and chemical activity in the surface waters of Govind Ballabh Pant Sagar reservoir. Various geochemical ratios showed the dominance of silicate over carbonate weathering and major ions such as Na+ + K+ account for about 52 % of the cation budget. The high Na+ and K+ showed sedimentation of rock/coal particles consisting of highly weathered silicate minerals contributed by the discharge of mine water, fly ash mixing during transportation, etc. Further, Ca2+ + Mg2+/Na+ + K+ ratio was <1 (0.92) indicating the occurrence of silicate weathering in the reservoir catchment. The comparative assessment showed that the proportion of Ca2+ + Mg2+/Na+ + K+ tends to be lower along the coal mining belts compared to non-coal mining regions in the world. The Ca2+/SO4 2? ratio <1 revealed not only H2CO3 but H2SO4 also acting as a source of protons for rock weathering. The cause underlying these differences can be related directly to geological substrate and anthropogenic activities.  相似文献   

15.
云南滇池地区风化磷块岩的风化指标研究   总被引:3,自引:0,他引:3  
黄毅  田升平 《矿物学报》1995,15(1):15-20
长期风化作用使云南滇池地区形成了大面积的风化磷块岩矿石,这种矿石是制取高效磷肥的优质原料。为了圈定这些风化磷块岩矿石,须确定适宜的风化指标。笔者通过风化磷块岩形成过程化学组分变化研究,首次提出将风化指标分为“直接法”和“间接法”两类,进而提出CO2风化指标为直接法中指标,2P2O5+A.I^1)风化指标为间接法中推荐指标。  相似文献   

16.
The techniques of electron paramagnetic resonance (EPR) were used to measure the concentration ratio of Eu2+ to Eu3+ in quenched silicate liquids as a function of their compositions. The compositional end members were CaAl2Si2O8 and either MSiO3 or M2Si04, M = Mg, (Ca0.5, Mg0.5), and Ca. All of the liquids were quenched from 1650 ± 25°C, 10?6.9±0.6 atm of oxygen, and 10?6.1±0.6 atm total pressure. For a particular choice of M, the ratio of Eu2+ to Eu3+ increased as much as a factor of 24 with increasing atomic ratio (Al + Si)/(O); for a constant value of (Al + Si)/(O), the ratio of Eu2+ to Eu3+ increased in the order Mg > (Ca0.5,Mg0.5) >Ca. In order to interpret the compositional dependence of the redox equilibrium of Eu in a systematic manner, the concept of a solvent coefficient was introduced.  相似文献   

17.
This paper reports original data on the physical and chemical parameters of precipitation, river water and groundwater in and around the Longhushan Nature Reserve Area, located in southwestern China karst region, and provides a preliminary characterization of the hydrogeochemical process governing the natural water evolution in this area. The rainfall and river water mainly pertain to the HCO3 –Ca2+ type and groundwater mainly pertain to the HCO3 –Ca2+ + Mg2+ type. The HCO3 was the predominant anion and Ca2+ was the predominant cation in all waters, respectively. The Gibbs Boomerang Envelop model, the 1:1 relationship of Na+ plus K+ versus Cl as well as the 1:1 relationship of Ca2+ plus Mg2+ versus HCO3 all suggested geochemical weathering is the main controlling factor for the geochemical compositions of this natural water. In surface water, the Mg2+/Ca2+ ratios ranged from 0.32 to 0.42 and the Na+/Ca2+ varied between 0.04 and 0.05. In the groundwater, the Mg2+/Ca2+ ratios varied from 0.37 to 0.62 and were below the ideal ratio of 0.8. These ratios showed the presence of a dolomite source. Analysis of trace elements showed that As, B, Pb, Se, Sr, V and Zn elements were abundant in the natural water during summer in this region.  相似文献   

18.
This study focused on the chemical compositions of the rivers around Yulong Mountain, one of the typical monsoonal temperate glacier regions in China. Water samples were collected from Baishui, Sanshu and Geji hydrological stations around Mt. Yulong during rainy season. The chemical analyses indicated that the river water around Mt. Yulong was characterized by high pH values (>8.0) and EC values varied from 36.4 to 71.7 μS/cm with an average of 52.6 μS/cm. Ca2+ and Mg2+ were the dominant cations, together accounting for about 90 % of the total cations. HCO3 ?, followed by SO4 2?, was the dominant anion. Obvious variations had been perceived during the rainy season. River water chemistry in rainy season was mainly influenced by precipitation and rock weathering. The proportions of Na+, K+, Ca2+, Mg2+ and SO4 2? from precipitation in river water were 23.44, 9.66, 3.10, 17.81 and 10.48 %, respectively. In addition, the ion characteristics of river water were mainly influenced by carbonate weathering. The human activities should not be ignored though its influence was little.  相似文献   

19.
A survey on quality of groundwater was carried out for assessing the geochemical characteristics and controlling factors of chemical composition of groundwater in a part of Guntur district, Andhra Pradesh, India, where the area is underlain by Peninsular Gneissic Complex. The results of the groundwater chemistry show a variation in pH, EC, TDS, Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ? and F?. The chemical composition of groundwater is mainly characterized by Na+?HCO3 ? facies. Hydrogeochemical type transits from Na+–Cl?–HCO3 ? to Na+–HCO3 ?–Cl? along the flow path. Graphical and binary diagrams, correlation coefficients and saturation indices clearly explain that the chemical composition of groundwater is mainly controlled by geogenic processes (rock weathering, mineral dissolution, ion exchange and evaporation) and anthropogenic sources (irrigation return flow, wastewater, agrochemicals and constructional activities). The principal component (PC) analysis transforms the chemical variables into four PCs, which account for 87% of the total variance of the groundwater chemistry. The PC I has high positive loadings of pH, HCO3 ?, NO3 ?, K+, Mg2+ and F?, attributing to mineral weathering and dissolution, and agrochemicals (nitrogen, phosphate and potash fertilizers). The PC II loadings are highly positive for Na+, TDS, Cl? and F?, representing the rock weathering, mineral dissolution, ion exchange, evaporation, irrigation return flow and phosphate fertilizers. The PC III shows high loading of Ca2+, which is caused by mineral weathering and dissolution, and constructional activities. The PC IV has high positive loading of Mg2+ and SO4 2?, measuring the mineral weathering and dissolution, and soil amendments. The spatial distribution of PC scores explains that the geogenic processes are the primary contributors and man-made activities are the secondary factors responsible for modifications of groundwater chemistry. Further, geochemical modeling of groundwater also clearly confirms the water–rock interactions with respect to the phases of calcite, dolomite, fluorite, halite, gypsum, K-feldspar, albite and CO2, which are the prime factors controlling the chemistry of groundwater, while the rate of reaction and intensity are influenced by climate and anthropogenic activities. The study helps as baseline information to assess the sources of factors controlling the chemical composition of groundwater and also in enhancing the groundwater quality management.  相似文献   

20.
Determining the relative proportions of silicate vs. carbonate weathering in the Himalaya is important for understanding atmospheric CO2 consumption rates and the temporal evolution of seawater Sr. However, recent studies have shown that major element mass-balance equations attribute less CO2 consumption to silicate weathering than methods utilizing Ca/Sr and 87Sr/86Sr mixing equations. To investigate this problem, we compiled literature data providing elemental and 87Sr/86Sr analyses for stream waters and bedrock from tributary watersheds throughout the Himalaya Mountains. In addition, carbonate system parameters (PCO2, mineral saturation states) were evaluated for a selected suite of stream waters. The apparent discrepancy between the dominant weathering source of dissolved major elements vs. Sr can be reconciled in terms of carbonate mineral equilibria. Himalayan streams are predominantly Ca2+-Mg2+-HCO3 waters derived from calcite and dolomite dissolution, and mass-balance calculations demonstrate that carbonate weathering contributes ∼87% and ∼76% of the dissolved Ca2+ and Sr2+, respectively. However, calculated Ca/Sr ratios for the carbonate weathering flux are much lower than values observed in carbonate bedrock, suggesting that these divalent cations do not behave conservatively during stream mixing over large temperature and PCO2 gradients in the Himalaya.The state of calcite and dolomite saturation was evaluated across these gradients, and the data show that upon descending through the Himalaya, ∼50% of the streams evaluated become highly supersaturated with respect to calcite as waters warm and degas CO2. Stream water Ca/Mg and Ca/Sr ratios decrease as the degree of supersaturation with respect to calcite increases, and Mg2+, Ca2+, and HCO3 mass balances support interpretations of preferential Ca2+ removal by calcite precipitation. On the basis of patterns of saturation state and PCO2 changes, calcite precipitation was estimated to remove up to ∼70% of the Ca2+ originally derived from carbonate weathering. Accounting for the nonconservative behavior of Ca2+ during riverine transport brings the Ca/Sr and 87Sr/86Sr composition of the carbonate weathering flux into agreement with the composition of carbonate bedrock, thereby permitting consistency between elemental and Sr isotope approaches to partitioning stream water solute sources. These results resolve the dissolved Sr2+ budget and suggest that the conventional application of two-component Ca/Sr and 87Sr/86Sr mixing equations has overestimated silicate-derived Sr2+ and HCO3 fluxes from the Himalaya. In addition, these findings demonstrate that integrating stream water carbonate mineral equilibria, divalent cation compositional trends, and Sr isotope inventories provides a powerful approach for examining weathering fluxes.  相似文献   

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