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1.
Chemical weathering of silicate minerals has long been known as a sink for atmospheric CO2, and feedbacks between weathering and climate are believed to affect global climate. While warmer temperatures are believed to increase rates of weathering, weathering in cool climates can be accelerated by increased mineral exposure due to mechanical weathering by ice. In this study, chemical weathering of silicate minerals is investigated in a small temperate watershed. The Jamieson Creek watershed is covered by mature coniferous forest and receives high annual precipitation (4000 mm), mostly in the form of rainfall, and is underlain by quartz diorite bedrock and glacial till. Analysis of pore water concentration gradients indicates that weathering in hydraulically unsaturated ablation till is dominated by dissolution of plagioclase and hornblende. However, a watershed scale solute mass balance indicates high relative fluxes of K and Ca, indicating preferential leaching of these solutes possibly from the relatively unweathered lodgement till. Weathering rates for plagioclase and hornblende calculated from a watershed scale solute mass balance are similar in magnitude to rates determined using pore water concentration gradients.When compared to the Rio Icacos basin in Puerto Rico, a pristine tropical watershed with similar annual precipitation and bedrock, but with dissimilar regolith properties, fluxes of weathering products in stream discharge from the warmer site are 1.8 to 16.2-fold higher, respectively, and regolith profile-averaged plagioclase weathering rates are 3.8 to 9.0-fold higher. This suggests that the Arrhenius effect, which predicts a 3.5- to 9-fold increase in the dissolution rate of plagioclase as temperature is increased from 3.4° to 22 °C, may explain the greater weathering fluxes and rates at the Rio Icacos site. However, more modest differences in K and Ca fluxes between the two sites are attributed to accelerated leaching of those solutes from glacial till at Jamieson Creek. Our findings suggest that under conditions of high rainfall and favorable topography, weathering rates of silicate minerals in warm tropical systems will tend to be higher than in cool temperate systems, even if the temperate system is has been perturbed by an episode of glaciation that deposits regolith high in fresh mineral surface area.  相似文献   

2.
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   

3.
Calcite is frequently cited as a source of excess Ca, Sr and alkalinity in solutes discharging from silicate terrains yet, no previous effort has been made to assess systematically the overall abundance, composition and petrogenesis of accessory calcite in granitoid rocks. This study addresses this issue by analyzing a worldwide distribution of more than 100 granitoid rocks. Calcite is found to be universally present in a concentration range between 0.028 to 18.8 g kg−1 (mean = 2.52 g kg−1). Calcite occurrences include small to large isolated anhedral grains, fracture and cavity infillings, and sericitized cores of plagioclase. No correlation exists between the amount of calcite present and major rock oxide compositions, including CaO. Ion microprobe analyses of in situ calcite grains indicate relatively low Sr (120 to 660 ppm), negligible Rb and 87Sr/86Sr ratios equal to or higher than those of coexisting plagioclase. Solutes, including Ca and alkalinity produced by batch leaching of the granitoid rocks (5% CO2 in DI water for 75 d at 25°C), are dominated by the dissolution of calcite relative to silicate minerals. The correlation of these parameters with higher calcite concentrations decreases as leachates approach thermodynamic saturation. In longer term column experiments (1.5 yr), reactive calcite becomes exhausted, solute Ca and Sr become controlled by feldspar dissolution and 87Sr/86Sr by biotite oxidation. Some accessory calcite in granitoid rocks is related to intrusion into carbonate wall rock or produced by later hydrothermal alteration. However, the ubiquitous occurrence of calcite also suggests formation during late stage (subsolidus) magmatic processes. This conclusion is supported by petrographic observations and 87Sr/86Sr analyses. A review of thermodynamic data indicates that at moderate pressures and reasonable CO2 fugacities, calcite is a stable phase at temperatures of 400 to 700°C.  相似文献   

4.
Concentrations of weathering products in streams often show relatively little variation compared to changes in discharge, both at event and annual scales. In this study, several hypothesized mechanisms for this “chemostatic behavior” were evaluated, and the potential for those mechanisms to influence relations between climate, weathering fluxes, and CO2 consumption via mineral weathering was assessed. Data from Loch Vale, an alpine catchment in the Colorado Rocky Mountains, indicates that cation exchange and seasonal precipitation and dissolution of amorphous or poorly crystalline aluminosilicates are important processes that help regulate solute concentrations in the stream; however, those processes have no direct effect on CO2 consumption in catchments. Hydrograph separation analyses indicate that old water stored in the subsurface over the winter accounts for about one-quarter of annual streamflow, and almost one-half of annual fluxes of Na and SiO2 in the stream; thus, flushing of old water by new water (snowmelt) is an important component of chemostatic behavior. Hydrologic flushing of subsurface materials further induces chemostatic behavior by reducing mineral saturation indices and increasing reactive mineral surface area, which stimulate mineral weathering rates. CO2 consumption by carbonic acid mediated mineral weathering was quantified using mass-balance calculations; results indicated that silicate mineral weathering was responsible for approximately two-thirds of annual CO2 consumption, and carbonate weathering was responsible for the remaining one-third. CO2 consumption was strongly dependent on annual precipitation and temperature; these relations were captured in a simple statistical model that accounted for 71% of the annual variation in CO2 consumption via mineral weathering in Loch Vale.  相似文献   

5.
Watershed mass-balance methods are valuable tools for demonstrating impacts to water quality from atmospheric deposition and chemical weathering. Owen Bricker, a pioneer of the mass-balance method, began applying mass-balance modeling to small watersheds in the late 1960s and dedicated his career to expanding the literature and knowledge of complex watershed processes. We evaluated long-term trends in surface-water chemistry in the Loch Vale watershed, a 660-ha. alpine/subalpine catchment located in Rocky Mountain National Park, CO, USA. Many changes in surface-water chemistry correlated with multiple drivers, including summer or monthly temperature, snow water equivalent, and the runoff-to-precipitation ratio. Atmospheric deposition was not a significant causal agent for surface-water chemistry trends. We observed statistically significant increases in both concentrations and fluxes of weathering products including cations, SiO2, SO4 2?, and ANC, and in inorganic N, with inorganic N being primarily of atmospheric origin. These changes are evident in the individual months June, July, and August, and also in the combined June, July, and August summer season. Increasingly warm summer temperatures are melting what was once permanent ice and this may release elements entrained in the ice, stimulate chemical weathering with enhanced moisture availability, and stimulate microbial nitrification. Weathering rates may also be enhanced by sustained water availability in high snowpack years. Rapid change in the flux of weathering products and inorganic N is the direct and indirect result of a changing climate from warming temperatures and thawing cryosphere.  相似文献   

6.
Flow-through dissolution experiments were carried out on crushed granitoid rock (the Elat Granite) and three mineral separates (plagioclase, perthite, and biotite + chlorite) from this rock at pH 1 and 25°C. Major element concentrations were combined with Pb and Sr isotopic analyses of starting materials and output solutions and together enabled us to elucidate several important mechanisms related to granitoid rock weathering. We observed an initial stage of rock dissolution (<200 hours of reaction) that was characterized by elemental release from traces of calcite and/or apatite and to a lesser extent from the interlayer sites of biotite. Dissolution in the interval of 200 to 400 h was dominated by the release of elements from the interlayer sites of biotite, and at 400 to 1000 h of reaction the chemistry of output solutions was dominated by the release of elements from tetrahedral and octahedral sites of biotite as well as from plagioclase. After 1000 h, the dissolution of plagioclase, and to a lesser extent biotite, dominated the composition of elements released by the rock. We demonstrate that Pb and Sr isotope ratios in the output solutions can be used to identify each of these stages of dissolution. By comparing our experimental results on the release of Pb and Sr isotopes with field measurements of Pb and Sr isotopes in soil chronosequences from the Wind River and the Sierra Nevada Mountains (USA), we are able to show that similar isotopic patterns appear in both the pH 1 experiments and in soils formed under natural conditions at higher pH. By combining these experimental results with previous field studies, we are able to estimate the duration of most of these stages of granitoid weathering under natural conditions in temperate climates. In soils older than a few hundred years and younger than 10,000 yr the release of elements from interlayer sites of biotite controls the weathering flux. Soils between 10,000 and 100,000 yr old are dominated by biotite and plagioclase weathering, with biotite weathering controlling the first part of this period and plagioclase dominating the later part. After more than 100,000 yr, plagioclase, and to a lesser degree biotite, dominate the weathering flux within these granitoid soils.  相似文献   

7.
We investigated chemical weathering in a high elevation granitic environment in three selected watersheds located in the Pyrenees (France). The sites were located on glacial deposits derived from similar Hercynian (∼300 Ma) granites characterized by the occurrence of zoned plagioclases and trace calcic phases (epidote, prehnite, sphene, apatite). The surface waters at those sites show high Ca/Na molar ratios (>1) which could not be explained by the dissolution of the major plagioclase (oligoclase) present in the rocks. The coupled approach of investigating stream water chemistry and the mineralogy and chemistry of rocks and soils allowed us to explore the role of the weathering of trace calcic minerals in calcium export at the watershed scale. The weathering of the trace calcic minerals which represent ∼ 1% of the total rock volume are responsible for more than 90% of the calcium export at the sites. Annual cationic fluxes (∼ 23.104 eq/km2/yr) calculated for the Estibère watershed are among the highest reported for high elevation systems draining granitic rocks and ∼ 80% of this annual cationic flux can be attributed to the weathering of trace calcic phases. Calculations based on isotopic values (87Sr/86Sr) go in the same direction. Except apatite, the trace calcic phases appear to be mainly silicates, thus the type of chemical weathering observed in the Estibère watershed may have an influence on atmospheric CO2 consumption by granite weathering. However, comparison with other watersheds draining granitic environments worldwide, and with the two other sites in the Pyrenees, indicate that the role of trace calcic phases is important in most young environments exposed to chemical weathering (e.g., high elevation catchments on glacial deposits). Other factors such as the date of glacial retreat, the physical denudation rate, the hydrological functioning of the watershed and the nature and structure of the soil cover are also important.  相似文献   

8.
Exhumation of the Himalayan-Tibetan orogen is implicated in the marked rise in seawater 87Sr/86Sr ratios since 40 Ma. However both silicate and carbonate rocks in the Himalaya have elevated 87Sr/86Sr ratios and there is disagreement as to how much of the 87Sr flux is derived from silicate weathering. Most previous studies have used element ratios from bedrock to constrain the proportions of silicate- and carbonate-derived Sr in river waters. Here we use arrays of water compositions sampled from the head waters of the Ganges in the Indian and Nepalese Himalaya to constrain the end-member element ratios. The compositions of tributaries draining catchments restricted to a limited range of geological units can be described by two-component mixing of silicate and carbonate-derived components and lie on a plane in multicomponent composition space. Key elemental ratios of the carbonate and silicate components are determined by the intersection of the tributary mixing plane with the planes Na = 0 for carbonate and constant Ca/Na for silicate. The fractions of Sr derived from silicate and carbonate sources are then calculated by mass-balance in Sr-Ca-Mg-Na composition space. Comparison of end-member compositions with bedrock implies that secondary calcite deposition may be important in some catchments and that dissolution of low-Mg trace calcite in silicate rocks may explain discrepancies in Sr-Ca-Na-Mg covariation. Alternatively, composition-dependent precipitation or incongruent dissolution reactions may rotate mixing trends on cation-ratio diagrams. However the calculations are not sensitive to transformations of the compositions by incongruent dissolution or precipitation processes provided that the transformed silicate and carbonate component vectors are constrained. Silicates are calculated to provide ∼50% of the dissolved Sr flux from the head waters of the Ganges assuming that discrepancies between Ca-Mg-Na covariation and the silicate rock compositions arise from addition of trace calcite. If the Ca-Mg-Na mixing plane is rotated by composition-dependent secondary calcite deposition, this estimate would be increased. Moreover, when 87Sr/86Sr ratios of the Sr inputs are considered, silicate Sr is responsible for 70 ± 16% (1σ) of the 87Sr flux forcing changes in seawater Sr-isotopic composition. Since earlier studies predict that silicate weathering generates as little as 20% of the total Sr flux in Himalayan river systems, this study demonstrates that the significance of silicate weathering can be greatly underestimated if the processes that decouple the water cation ratios from those of the source rocks are not properly evaluated.  相似文献   

9.
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   

10.
Based on the geological background, R-mode factor statistics, and the analysis of the stability diagram for the corresponding system, five weathering reactions controlling the surface-water chemical composition in the watershed of the Changhuajiang River are deduced. In the mass balance model, the precipitation accounts for some solute input, since the rainwater is dilute without pollution. Most of the Ca2+ and HCO 3 – ions are from the dissolution of calcite, K+, Na+, H4SiO4 and some of the Mg2+ and HCO 3 – come from albite and biotite weathering to kaolinite. The dissolution of dolomite and gypsum controls the mass balances of Mg2+ and SO 4 2– . The dissolution of calcite is the dominant chemical weathering reaction in the watershed because of its reactivity and high concentration. In the watershed in 1986, the chemical weathering rate was 0.073 (kg/m2 a), and the mechanical denudation rate is 0.093 (kg/m2 a). The chemical weathering mass output proportion of carbonate rocks to silicate rocks was about three to one.  相似文献   

11.
It is widely accepted that chemical weathering of Ca–silicate rocks could potentially control long-term climate change by providing feedback interaction with atmospheric CO2 drawdown by means of precipitation of carbonate, and that in contrast weathering of carbonate rocks has not an equivalent impact because all of the CO2 consumed in the weathering process is returned to the atmosphere by the comparatively rapid precipitation of carbonates in the oceans. Here, it is shown that the rapid kinetics of carbonate dissolution and the importance of small amounts of carbonate minerals in controlling the dissolved inorganic C (DIC) of silicate watersheds, coupled with aquatic photosynthetic uptake of the weathering-related DIC and burial of some of the resulting organic C, suggest that the atmospheric CO2 sink from carbonate weathering may previously have been underestimated by a factor of about 3, amounting to 0.477 Pg C/a. This indicates that the contribution of silicate weathering to the atmospheric CO2 sink may be only 6%, while the other 94% is by carbonate weathering. Therefore, the atmospheric CO2 sink by carbonate weathering might be significant in controlling both the short-term and long-term climate changes. This questions the traditional point of view that only chemical weathering of Ca–silicate rocks potentially controls long-term climate change.  相似文献   

12.
Dissolved rare earth elements (REEs) were determined in a four-year time series at the outlet of Loch Vale. The Loch Vale watershed is a seasonally snow-covered alpine/subalpine basin in Rocky Mountain National Park, USA. The time series was mainly distinguished by an annual early spring peak in the concentrations of all REEs. REE concentrations at this time were as much as 8-fold greater than at other times of the year. This annual peak was coincident with an early spring peak in dissolved organic carbon (DOC) which results from flushing of soils at the beginning of spring snow melting. The REE/DOC peak occurs as discharge starts to increase from wintertime lows but well before the spring peak in discharge. Speciation considerations suggest complexation of the REEs by DOC. The Ce anomaly also increases (i.e., is less fractionated) during the spring flush indicating that the most reducing (or least oxidizing) REE sources in the system are comparatively more important at that time. Mn data and the La/Yb ratio also support this. The behavior of REEs in the Loch Vale system has additionally been compared with metal and DOC behavior in other systems. Hydrologic and climatic differences can be important especially with regard to timing and duration of the spring flush peak. Damping of hydrologic events in the lower floodplain of major rivers may also partially result in the differences observed between Loch Vale and the lower Mississippi River. However, comparison with the Amazon River system additionally suggests that seasonal flooding of wetlands may be an important regulator of REE concentrations. Chemical differences are also important for these systems. This includes pH and suspended matter concentrations which affect the balance between adsorption and complexation. Additionally, the relative complexing ability of DOC in different systems is a factor needing further consideration.  相似文献   

13.
The study of biogeochemical and hydrological cycles in small experimental watersheds on silicate rocks, common for the Temperate Zone, has not yet been widely applied to the tropics, especially humid areas. This paper presents an updated database for a six-year period for the small experimental watershed of the Mengong brook in the humid tropics (Nsimi, South Cameroon). This watershed is developed on Precambrian granitoids (North Congo shield) and consists of two convexo-concave lateritic hills surrounding a large flat swamp covered by hydromorphic soils rich in upward organic matter. Mineralogical and geochemical investigations were carried out in the protolith, the saprolite, the hillside lateritic soils, and the swamp hydromorphic soils. Biomass chemical analyses were done for the representative species of the swamp vegetation. The groundwater was analysed from the parent rock/saprolite weathering front to the upper fringe in the hillside and swamp system. The chemistry of the wet atmospheric and throughfall deposits and the Mengong waters was monitored.In the Nsimi watershed the carbon transfer occurs primarily in an organic form and essentially as colloids produced by the slow biodegradation of the swamp organic matter. These organic colloids contribute significantly to the mobilization and transfer of Fe, Al, Zr, Ti, and Th in the uppermost first meter of the swamp regolith. When the organic colloid content is low (i.e., in the hillside groundwater), Th and Zr concentrations are extremely low (<3 pmol/L, ICP-MS detection limits). Strongly insoluble secondary thorianite (ThO2) and primary zircon (ZrSiO4) crystals control their mobilization, respectively. This finding thus justifies the potential use of both these elements as inert elements for isoelement mass balance calculations pertaining to the hillside regolith.Chloride can not be used as a conservative tracer of hydrological processes and chemical weathering in this watershed. Biogenic recycling significantly influences the low-Cl input fluxes. Sodium is a good tracer of chemical weathering in the watershed. The sodium solute flux corrected from cyclic salt input was used to assess the chemical weathering rate. Even though low (2.8 mm/kyr), the chemical weathering rate predominates over the mechanical weathering rate (1.9 mm/kyr). Compared to the Rio Icacos watershed, the most studied tropical site, the chemical weathering fluxes of silica and sodium in the Mengong are 16 and 40 times lower, respectively. This is not only related to the protective role of the regolith, thick in both cases, but also to differences in the hydrological functioning. This is to be taken into account in the calculations of the carbon cycle balance for large surfaces like that of the tropical forest ecosystems on a stable shield at the global level.  相似文献   

14.
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   

15.
渝东北黑色页岩元素迁移特征及化学风化程度   总被引：1，自引：0，他引：1       下载免费PDF全文
黑色页岩是富含有机质和硫化矿物的特殊沉积岩,但人们对其风化过程的元素活动性及矿物风化机制关注较少.为探讨不同地形位置的黑色页岩化学风化过程,采集了渝东北城口某山脊 (A)、近山顶 (B) 和沟谷 (C) 的下寒武统水井沱组黑色页岩风化剖面岩样,利用XRD、XRF和化学分析手段对采集样品的矿物成分、主量元素进行测定分析.元素和矿物的质量迁移系数 (τ) 和质量迁移通量 (Mj, flux) 的计算结果表明,黑色页岩风化过程中Ca、Mg和Na元素具有明显的贫化现象,近地表处存在Al元素的富集现象;矿物成分方面,黄铁矿和有机质氧化后形成的酸性水环境,造成方解石、白云石、斜长石等不稳定矿物溶解,并生成含水石膏、铁质氧化物、黏土矿物等次生矿物.不同赋存位置的黑色页岩风化程度有所差异,Na/K-CIA、K/Ca*-Al/Na、A-CN-K和A-CNK-FM图解显示:A剖面处于脱Ca过程的初级风化阶段,B剖面处于脱Ca、Na初期的初等-中等风化阶段,C剖面已发生脱Ca、Na过程,并伴随脱Si作用的中等-强烈风化阶段,结合不同风化指数 (如:CIA、CIW、PIA、MWPI等),得出各剖面的化学风化强弱程度依次为C＞B＞A.   相似文献   

16.
花岗岩目前的ISMA分类不是一个系统的分类,花岗岩分类可能需要从花岗岩的起源来考虑。花岗岩源自变质岩,可能是来自地幔或玄武质岩浆底侵带来的热导致的下地壳底部发生部分熔融的熔体形成的。因此,花岗岩与变质岩源岩有成因联系和因果关系,变质岩为母,花岗岩为子。根据埃达克岩与残留相平衡的理论,埃达克岩形成于斜长石消失线之上。那么,出现在石榴石出现线之上的是什么花岗岩呢?出现在石榴石出现线之下的又是什么花岗岩呢?本文即尝试从这个思路来探讨花岗岩的分类,并采用大数据方法予以佐证,得到的初步结果可以将花岗岩分为3类:(1)位于斜长石消失线之上的为高Sr低Y型花岗岩(高压,代表加厚的地壳);(2)位于斜长石消失线与石榴石出现线之间的为低Sr低Y类型花岗岩(中压,代表正常厚度的地壳);(3)位于石榴石出现线之下的为高Y型花岗岩(低压,代表减薄的地壳)。大数据研究的结果支持上述分类,给出的地球化学标志大体是:Sr含量为400×10-6,Y含量为(20~35)×10-6。  相似文献   

17.
《Applied Geochemistry》1999,14(2):237-254
Two major types of groundwater can be readily distinguished in the Variscian crystalline basement of the Black Forest in S–W Germany. Saline thermal water utilized in spas has its origin in 3–4 km deep reservoirs and developed its composition by 3 component mixing of surface freshwater, saltwater (of ultimately marine origin) and a water–rock reaction component. In contrast to the thermal water, CO2-rich mineral water, tapped and bottled from many wells in the Black Forest, has low salinities but a TDS distribution similar to that of thermal water. It developed its chemical composition entirely by reaction of CO2-rich water with the gneissic or granitic aquifer rock matrix. Particularly important is the contribution of various plagioclase dissolution and weathering reactions that may, at some locations, involve precipitation and dissolution of secondary calcite. Sodium/Ca ratios of water and of rock forming plagioclase in the basement rocks suggests that plagioclase weathering is strongly incongruent. Calcium is released to the water, whereas Na remains fixed to the albite feldspar component.The major element composition of 192 water samples used in this study also indicates a clear vertical stratification of the type of water chemistry; Ca–HCO3 near the surface, Na–Ca–HCO3–SO4 at intermediate depth and Na–Ca–Cl at great depth.The mean permeability of Black Forest granite is about K=10−6 m/s; it is significantly lower in gneisses (gneiss: mean K=5×10−8 m/s) leading to focused flow through granite. Highly permeable fracture and fault zones, particularly in granite, are utilized by high-TDS saline deep groundwater as ascent channels and flow paths. Although spatially closely associated, the topography driven upwelling system of saline deep water and the near-surface flow system of CO2-rich mineral waters are hydraulically and chemically unconnected.  相似文献   

18.
This work focuses on developing multidisciplinary research on weathering profiles of granitoid rocks related to the tectonic and landscape evolution of the Capo Vaticano area, Calabria, southern Italy. During the Pleistocene, the Mediterranean climate plays, on the already decomposed plutonic rocks, important processes of alteration, on both the highest and inland areas and the coastal areas of the Calabrian region, such as the studied area. Field observations coupled to chemical, minero‐petrographical features and geochemical modelling are used to characterize the weathering processes affecting the granitoid complex. The granitoid cut slopes show a generally simple weathering profile characterized by a progressive increase in weathering towards the top of the slopes. The completely weathered rocks (class V) and residual soil (class VI) contain a high percentage of altered minerals, microfractures, and voids. The main mineralogical changes are the partial transformation of biotite and the partial destruction of feldspars (mainly plagioclase) that are associated with the neoformation of secondary clay minerals and ferruginous products during the most advanced stage of weathering. These transformations produce a substitution of the original rock fabric. Geochemical modelling showing the precipitation of kaolinite, illite, vermiculite, ferrihydrite and calcite. These secondary solid phases are similar to those found in this natural system. Thus, the final results of the weathering process is a soil‐like material mainly characterized by mostly a sand to gravel grain‐size fractions related to microfabric changes and mineralogical and chemical variations. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

19.
We explored changes in the relative importance of carbonate vs. silicate weathering as a function of landscape surface age by examining the Ca/Sr and Sr isotope systematics of a glacial soil chronosequence located in the Raikhot watershed within the Himalaya of northern Pakistan. Bedrock in the Raikhot watershed primarily consists of silicate rock (Ca/Sr ≈ 0.20 μmol/nmol, 87Sr/86Sr ≈ 0.77 to 1.2) with minor amounts of disseminated calcite (Ca/Sr ≈ 0.98 to 5.3 μmol/nmol, 87Sr/86Sr ≈ 0.79 to 0.93) and metasedimentary carbonate (Ca/Sr ≈ 1.0 to 2.8 μmol/nmol, 87Sr/86Sr ≈ 0.72 to 0.82). Analysis of the exchangeable, carbonate, and silicate fractions of seven soil profiles ranging in age from ∼0.5 to ∼55 kyr revealed that carbonate dissolution provides more than ∼90% of the weathering-derived Ca and Sr for at least 55 kyr after the exposure of rock surfaces, even though carbonate represents only ∼1.0 wt% of fresh glacial till. The accumulation of carbonate-bearing dust deposited on the surfaces of older landforms partly sustains the longevity of the carbonate weathering flux. As the average landscape surface age in the Raikhot watershed increases, the Ca/Sr and 87Sr/86Sr ratios released by carbonate weathering decrease from ∼3.6 to ∼0.20 μmol/nmol and ∼0.84 to ∼0.72, respectively. The transition from high to low Ca/Sr ratios during weathering appears to reflect the greater solubility of high Ca/Sr ratio carbonate relative to low Ca/Sr ratio carbonate. These findings suggest that carbonate weathering controls the dissolved flux of Sr emanating from stable Himalayan landforms comprising mixed silicate and carbonate rock for tens of thousands of years after the mechanical exposure of rock surfaces to the weathering environment.  相似文献   

20.
This paper focuses on reasons for the appearance of tetrad effects in chondrite-normalized REE distribution patterns of granitoids (Li-F granites, peralklaine granites, ongonites, fluorine-rich rhyolites, and granitic pegmatites). The analysis of published data showed that the alteration of such rocks by high- and/or low-temperature metasomatic processes does not result in most cases in the appearance or enhancement of M-type tetrad effects in REE patterns. These processes are accompanied by the removal or addition of lanthanides, a W-type sag appears between Gd and Ho, and negative or positive Ce anomalies develop sometimes in REE patterns. The formation conditions of peculiar rocks enriched in Ca and F from the Ary Bulak ongonite massif (eastern Transbaikalia) and the character of REE distribution in these rocks and melt inclusion glasses were discussed. Based on the obtained data and the analysis of numerous publications, it was concluded that REE tetrad effects in rare-metal granitoids are caused by fluoride-silicate liquid immiscibility and extensive melt differentiation in the accumulation chambers of fluorine-rich magmas. A considerable increase in fluorine content in a homogeneous granitoid melt can cause its heterogenization (liquation) and formation of fluoride melts of various compositions. The redistribution of lanthanides between the immiscible liquid phases of granitoid magma will result in the formation of M-type tetrad effects in the silicate melts, because the REE patterns of fluoride melts exhibit pronounced W-type tetrad effects. The maximum M-type tetrad effect between La and Nd, which is observed in many rare-metal granitoids, is related to the character of REE partitioning between fluoride and silicate melts and F- and Cl-rich magmatic fluids. The low non-chondritic Y/Ho ratio (<15) of many rare-metal granitoids may be indicative of a contribution of fluoride melts to the differentiation of F-rich silicic magmas, from which these rocks were formed. The influence of high-temperature F-Cl-bearing fluids on melts and/or granitoid rocks results in an increase in Y/Ho ratio owing to the elevated solubility of Ho in such fluids.  相似文献   

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