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1.
Apatite dissolution experiments were conducted using both a fluidized bed and stirred tank reactor over a range of pH, temperature, solution saturation state, and on non-carbonated and carbonated apatite compositions: igneous fluorapatite (FAP) and sedimentary carbonate fluorapatite (CFA), respectively. From 2 <pH <6, the rate of release from dissolution of all apatite components [calcium (Ca), phosphorus (P), and fluoride (F)] increased with decreasing pH for FAP. From 6 < pH < 8.5, the FAP dissolution rate is pH independent. Measuring apatite dissolution rates at pH > 8.5 were not possible due to detection limits of the analytical techniques used in this study and the high insolubility of FAP. For the CFA compositions studied, the dissolution rate decreased with increasing pH from 4 < pH < 7. During early stages of the dissolution reaction for both FAP and CFA, mineral components were released in non-stoichiometric ratios with reacted solution ratios of dissolved Ca:P and Ca:F being greater than mineral stoichiometric ratios, suggesting that Ca was preferentially released compared to P and F from the mineral structure during the early stages of dissolution. An increase in reacted solution pH accompanies this early elevated release of Ca. As the dissolution reaction proceeded to steady state, dissolution became congruent. When normalized to BET measured surface area, FAP dissolved faster from 4 < pH < 7 compared to CFA. The apparent Arrhenius activation energy (Ea) of FAP dissolution over the temperature range of 25-55°C at pH = 3.0, I = 0.1, and pCO2 = 0 is 8.3 ± 0.2 kcal mol−1. Both the apparent exchange of solution H+ for solid-bound Ca at low pH in the early stage of dissolution and the Ea of dissolution suggest a surface and not a diffusion controlled dissolution reaction for FAP and CFA. The degree of undersaturation of the solution, ΔGR, with respect to FAP was important in determining the dissolution rate. At pH = 3.0, I = 0.1, and pCO2 = 0, the dissolution rate of FAP was ∼ 5× greater in the far-from-equilibrium region compared to the near-equilibrium slope region.A simple apatite weathering model incorporating the experimental results from this study was constructed, and numerical calculations suggest that during the Phanerozoic both the surface area of igneous rock available for weathering and the average global temperature were important factors in determining the P weathering flux from apatite dissolution. It is possible that elevated global temperatures coupled with relatively high surface area of igneous rock during the early- to mid-Paleozoic resulted in elevated P weathering fluxes, which along with climatic evolutionary pressures of the Neoproterozoic, facilitated the radiation of multicellular organisms, large-scale phosphorite deposition, and abundance of calcium phosphate shelled organisms during the early Cambrian. 相似文献
2.
长期的风化会使遗址土体劣化,进而威胁到遗址本体的安全,但在自然条件下这一演化过程尚不明确。遗址土体微观结构的变化是该过程的重要体现,研究选取风化条件近似而暴露时间不同的黄土质边坡作为类比对象,采用扫描电镜法（SEM）和压汞法（MIP）分别对表部以及内部土样的微观孔隙结构进行观察和量测。试验结果表明,表部土体微观结构的变化程度大于内部土体,并呈现一定的规律性;与内部土体相比,表部土体的土颗粒排列为致密的叠片状;其孔径分布为双峰模式,团聚体内孔隙占比较大;随着风化时间的增长,表部土体的孔隙总体积和表面分形维数逐渐减小,导致孔壁粗糙程度降低,减小了颗粒间的摩擦,在宏观上容易诱发土体表层的剥离损耗或其他病害。 相似文献
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Chemical weathering gradients are defined by the changes in the measured elemental concentrations in solids and pore waters with depth in soils and regoliths. An increase in the mineral weathering rate increases the change in these concentrations with depth while increases in the weathering velocity decrease the change. The solid-state weathering velocity is the rate at which the weathering front propagates through the regolith and the solute weathering velocity is equivalent to the rate of pore water infiltration. These relationships provide a unifying approach to calculating both solid and solute weathering rates from the respective ratios of the weathering velocities and gradients. Contemporary weathering rates based on solute residence times can be directly compared to long-term past weathering based on changes in regolith composition. Both rates incorporate identical parameters describing mineral abundance, stoichiometry, and surface area.
Weathering gradients were used to calculate biotite weathering rates in saprolitic regoliths in the Piedmont of Northern Georgia, USA and in Luquillo Mountains of Puerto Rico. Solid-state weathering gradients for Mg and K at Panola produced reaction rates of 3 to 6×10−17 mol m−2 s−1 for biotite. Faster weathering rates of 1.8 to 3.6×10−16 mol m−2 s−1 are calculated based on Mg and K pore water gradients in the Rio Icacos regolith. The relative rates are in agreement with a warmer and wetter tropical climate in Puerto Rico. Both natural rates are three to six orders of magnitude slower than reported experimental rates of biotite weathering. 相似文献
5.
Noye M. Johnson Charles T. Driscoll John S. Eaton Gene E. Likens William H. McDowell 《Geochimica et cosmochimica acta》1981,45(9):1421-1437
Contemporary ‘acid rain’ in the Hubbard Brook ecosystem has induced a series of geochemical responses. Neutralization is accomplished in essentially a 2-step process. Initially, hydrogen ion acidity is neutralized by the dissolution of reactive alumina primarilly found in the soil zone. In the Hubbard Brook area this reactive alumina has solution properties much like natural gibbsite. Aluminum-rich surface waters with a pH of 4.7 5.2 are typical of this neutralization stage. In a second step, both hydrogen ion acidity and aluminum acidity are neutralized by the chemical weathering of primary silicate minerals, i.e. by the alkali and alkaline earths contained in the bedrock and glacial till of the watershed. The chemical weathering reaction is much slower than the alumina dissolution reaction, so that the aluminum acidity stage (pH 4.7 5.2) may persist for substantial periods. Typically, however, in the Hubbard Brook area the aluminum acidity has been neutralized and a pH > 5.2 is obtained before surface waters reach a third-over stream channel. Because of the relatively low pH's throughout the soil zone and in the streamwater, carbonic acid reactions are essentially absent at the present time in the Hubbard Brook system. Water pathlength (or residence time) in the soil zone is the crucial factor in the state of acid rain neutralization, aluminum chemistry and chemical weathering. As measured by the losses of alkali and alkaline earths from the ecosystem, chemical weathering rate in the Hubhard Brook area at the present time is not especially high relative to other areas. 相似文献
6.
鄂尔多斯盆地下古生界马家沟组顶部遭受长期风化剥蚀,形成了以膏云岩为主的风化壳岩溶储层。通过偏光显微和超微扫描电镜深入观察了（含）膏云岩的孔隙类型及充填规律,分析了其岩溶作用特点,研究了以膏云岩为主的岩溶作用特征与传统碳酸盐岩岩溶作用特征的区别,探讨了膏云岩发育区的岩溶作用模式。结果表明:硬石膏结核和石膏晶体以其强亲水性和远高于白云石、方解石的溶解度,极易率先吸水发生溶解形成组构选择性溶蚀孔隙,导致膏云岩层蜂窝状溶孔的形成。硬石膏的高溶解度和力学不稳定性使得研究区以膏云岩、白云岩和灰云岩互层的风化壳储层以膏模孔、扩溶膏模孔及与之伴生的胀缩微裂缝为主要储集空间,孔隙大小具有明显的自限性。岩性—（含）膏云岩和沉积微相—海平面低位期潮上带（含）膏云坪沉积是储层形成的先天物质基础和环境条件,并因此直接导致（含）膏云岩储层的成层分布特征。表层膏云岩首先遭受淡水淋滤形成蜂窝状溶孔,多层成层分布膏云岩这种独特的物理化学性质使风化壳内的岩溶水以弥散性渗透为主,这是膏云岩发育区岩溶作用特征和模式与碳酸盐岩产生重要差异的根本原因。 相似文献
7.
Grasslands of north-central Kansas are underlain by carbonate aquifers and shale aquitards. Chemical weathering rates in carbonates are poorly known, and, because large areas are underlain by these rocks, solute fluxes are important to estimating global weathering rates. Grasslands exist where the amount of precipitation is extremely variable, both within and between years, so studies in grasslands must account for changes in weathering that accompany changes in precipitation. This study: (1) identifies phases that dominate chemical fluxes at Konza Prairie Biological Station (KPBS) and Long-Term Ecological Research Site, and (2) addresses the impact of variable precipitation on mineral weathering. The study site is a remnant tallgrass prairie in the central USA, representing baseline weathering in a mid-temperate climate grassland.Groundwater chemistry and hydrology in the 1.2 km2 watershed used for this study suggest close connections between groundwater and surface water. Water levels fluctuate seasonally. High water levels coincide with periods of precipitation plus low evapotranspiration rather than during precipitation peaks during the growing season. Precipitation is concentrated before recharging aquifers, suggesting an as yet unquantified residence time in the thin soils.Groundwater and surface water are oversaturated with respect to calcite within limitations of available data. Water is more dilute in more permeable aquifers, and water from one aquifer (Morrill) is indistinguishable from surface water. Cations other than Ca co-vary with each other, especially Sr and Mg. Potassium and Si co-vary in all aquifers and surface water, and increases in concentrations of these elements are the best indicators of silicate weathering at this study site. Silicate-weathering indices correlate inversely to aquifer hydraulic conductivity.87Sr/86Sr in water ranges from 0.70838 to 0.70901, and it decreases with increasing Sr concentration and with increasing silicate-weathering index. Carbonate extracted from aquifer materials, shales, soil, and tufa has Sr ranging from about 240 (soil) to 880 ppm (Paleozoic limestone). 87Sr/86Sr ranges from 0.70834 ± 0.00006 (limestone) to 0.70904 ± 0.00019 (soil). In all cases, 87Sr/86Sr of aquifer limestone is lower than 87Sr/86Sr of groundwater, indicating a phase in addition to aquifer carbonate is contributing solutes to water.Aquifer recharge controls weathering: during periods of reduced recharge, increased residence time increases the total amount of all phases dissolved. Mixing analysis using 87Sr/86Sr shows that two end members are sufficient to explain sources of dissolved Sr. It is proposed that the less radiogenic end member is a solution derived from dissolving aquifer material; longer residence time increases its contribution. The more radiogenic end member solution probably results from reaction with soil carbonate or eolian dust. This solution dominates solute flux in all but the least permeable aquifer and demonstrates the importance that land-surface and soil-zone reactions have on groundwater chemistry in a carbonate terrain. 相似文献
8.
In the study of surface processes, it is generally assumed that erosion occurs equally throughout the soil profile so that chemical depletion of the topsoil can represent the intensity of chemical weathering and the duration of surface exposure to cosmogenic radiation can reflects the soil residence time, and then the rate of erosion can be calculated. In comparison with fresh bedrock, the depletion of soluble elements in soil mainly comes from fine-grained secondary clay components, while the depletion degree of detrital minerals is weak. The preferential erosion of fine-grained secondary clay will lead to the underestimation of weathering intensity, and the retention time of detrital mineral will be longer than the total retention time of soil， and thus the soil erosion rate will be underestimated. Based on the uranium isotope comminution ages of soil in the Lesotho Highlands, we found that erosion operates differentially between the detrital and authigenic components of the soil. Uranium isotope comminution ages show a soil residence time of (543±32) ka for the detrital particles. In contrast, soil residence time of the authigenic phases is constrained to be (22±11) ka according to the accumulation of recoiled 234U from the absorbed 238U to river water. The residence time of secondary clay matches with the regional erosion rate 24-33 t/(km2·a) calculated from weathering flux, indicating that secondary clay is the main component of soil erosion. The results indicate that the decoupled erosion of different components in soil may be common. This finding implies that the intensity of weathering based on bulk soil erosion and the rate of soil erosion determined by exposure dating of coarse soil grains may be invalidated due to the preferential erosion of authigenic particles. As a result, a lower estimate of weathering flux may be made, and therefore the role of chemical weathering in the global carbon cycle could be underestimated. 相似文献
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Julie D. Stopar G. Jeffrey Taylor Victoria E. Hamilton Lauren Browning 《Geochimica et cosmochimica acta》2006,70(24):6136-6152
If water was ever present on Mars, as suggested by geomorphological features, then much of the surface and subsurface may have experienced chemical weathering. Among those materials most readily altered is olivine, which has been identified on the Martian surface with IR spectroscopy and Mossbauer techniques and occurs in Martian meteorites. We use geochemical models of olivine dissolution kinetics to constrain the residence time of olivine on the surface of Mars in the presence of liquid water. From these models, we have calculated maximum dissolution rates and minimum residence times for olivine as a function of temperature, pH, Fe-composition, and particle size. In general, the most favorable conditions for olivine dissolution are fayalite-rich compositions, small particle sizes, high temperatures, and acidic solutions that are far from equilibrium. The least favorable conditions for olivine dissolution are forsterite-rich compositions, large particle sizes, ultra-low temperatures, and a neutral pH solution near equilibrium. By using kinetic models of olivine dissolution to bound dissolution rates and residence times, we can make inferences about the temporal extent of aqueous alteration on the surface of Mars. Under favorable conditions (pH 2, 5 °C, and far from equilibrium) a relatively large 0.1 cm (radius) particle of Fo65 composition can completely dissolve in 370 years. Particles may last 102–104 times longer under less favorable conditions. However, residence times of a few million years or less are small compared to the age of most of the Martian surface. The survival of olivine on the surface of Mars, especially in older terrains, implies that contact with aqueous solutions has been limited and wet periods on Mars have been short-lived. 相似文献
11.
Since July 2002, tertiary treated wastewater has been artificially recharged through two infiltration ponds in the dunes of the Belgian western coastal plain. This has formed a lens of artificially recharged water in the dunes’ fresh water lens. Recharged water is recovered by extraction wells located around the ponds. Hydraulic aspects of the artificial recharge and extraction are described using field observations such as geophysical borehole loggings and a tracer test. Borehole logs indicate recharged water up to 20 m below surface, whereas the tracer test gives field data about the residence times of the recharged water. Furthermore, a detailed solute transport model was made of the area surrounding the ponds. Groundwater flow, capture zone, residence times and volume of recharged water in the aquifer are calculated. This shows that the residence time varies between 30 days and 5 years due to the complex flow pattern. The extracted water is a mix of waters with different residence times and natural groundwater, assuring a relatively stable water quality of the extracted water. 相似文献
12.
John R. Watterson 《Precambrian Research》1985,30(4):321-335
Many of the world's richest gold placer deposits now occur in cold regions despite differences in their climatic history. It therefore seems possible that there may be some fundamental connection between freezing climates and the local chemical behavior of gold in the weathering cycle. This hypothesis, along with the problematical occurrence of gold as euhedral crystals in arctic gravel and soil placers, has led me to review low temperature phenomena that may bear on the geochemistry of gold.Several effects which may influence the weathering of natural gold-bearing rocks, the chemical complexation of gold, and its subsequent mobility and deposition appear to be strongly connected with freeze action. The exclusion of dissolved solutes, solute gases, and particles from ice, subjects rock and soil minerals to increased corrosion from thin, unfrozen, adsorbed water films which remain at particle surfaces throughout the freezing of rocks and soils. The preferential exclusion of cations (over anions) from growing ice crystals creates charge separations and measurable current flow across waterice phase boundaries in freezing soil — a phenomenon which leads to troublesome seasonal electrolytic corrosion of pipelines buried in soil; this phenomenon may also favor the dissolution of normally insoluble metals such as gold during geologic time periods. The ice-induced accumulation of clays, organic acids, bacteria, and other organic matter at mineral surfaces may also speed chemical attack by providing a nearby sink of alternate cation-binding sites and hence rapid removal of liberated cations from solution. The latter mechanism may be operative in both the dissolution and redeposition of gold.These physical, chemical, and electrical effects are favorable to the dissolution of rocks (in addition to frost shattering) and to the dissolution, mobilization, and redeposition of gold and other noble metals and must therefore contribute significantly to the behavior of gold at low temperatures. The occurrence of large numbers of gold placer deposits in northern Canada, Alaska, and Siberia may thus be due in part to the low temperatures common to these regions. 相似文献
13.
文章通过大量岩芯、铸体薄片观察和测井资料分析,对准噶尔腹部石西石炭系火山岩风化壳储层进行了详细地研究。研究结果表明,该火山岩风化壳储层的储集空间主要有基质溶孔、气孔或杏仁体溶孔、角砾间溶孔、微裂缝和裂缝等,其中与裂缝连通的各类溶孔占主导地位;在岩石分布上以集块岩、条带状熔岩、角砾熔岩和致密凝灰岩为主,玄武岩、安山岩和流纹岩则相对较少;储层物性主要表现为高孔低渗,只有裂缝具有较高的渗透率,且裂缝以高角度缝和直立缝为主。研究还发现,岩性岩相、裂缝和风化淋滤作用是影响该风化壳储层的主要因素。区内油层主要聚中在构造高部位、靠近断裂带和有利岩相区域;油层分布在离石炭系风化壳顶面25~150 m的范围内。 相似文献
14.
柴达木盆地阿尔金山前斜坡带发现了规模分布的东坪基岩气田,其基岩风化壳的作用成为关注的问题。依据元素分析、X-射线衍射分析、岩心薄片观察,常规测井响应和成像测井响应特征,识别出东坪地区基岩风化壳发育不同结构层,且不同结构层的储集特征有很大差异。研究表明,基岩风化壳结构可划分为土壤层、完全风化层和半风化层,而半风化层又可进一步分为溶蚀带和崩解带;其中土壤层厚度0~2 m,完全风化层厚度4~15 m,溶蚀带厚度365~164 m,崩解带厚度300~1 000 m。基岩半风化层是储层发育带,其中溶蚀带储集物性好于崩解带,溶蚀带发育较多的溶蚀孔洞和溶蚀加宽的网状裂缝,孔隙度范围2%~16%;而崩解带发育弱溶蚀构造缝和节理缝,孔隙度范围2%~8%。东坪地区大规模发育基岩风化壳为柴达木盆地远离烃源岩灶的斜坡地区寻找油气提供了借鉴依据。 相似文献
15.
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
16.
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
17.
碳酸盐岩差异性风化成土特征及其对石漠化形成的影响 总被引：35，自引：0，他引：35
碳酸盐岩极低的酸不溶物含量使岩石风化产生的残积土壤物质数量极少，并产生巨大的体积缩小，促使早期形成的残积土在重力作用下不断向下塌陷。显著的差异性风化使基岩面强烈起伏，甚至形成大量的岩溶尘洼地、裂隙、地下管道、洞穴系统等。在重力和水的作用下，土粒沿垂直和水平方向上经微距离或短距离搬运到上述低洼或地下空间中，甚至由地下河带到更远的地方，这是碳酸盐岩地区土壤丢失的重要方式，也是形成石漠化最主要的地质因素。土壤在地表分布高度不均匀，是碳酸盐岩地区的地表少土的重要原因。对于酸不溶物含量相当的石灰岩和白云岩而言，由于白云岩的差异性风化明显弱于石灰岩，以及受各种应力作用后，白云岩形成的节理及裂隙密集而均匀，从而提高了近地表白云岩的含水能力，延长了风化过程中的水－岩反应时间，使风化作用可以相对集中于地表或近地表进行，有利于岩石的整体风化作用的进行，同时使白云岩风化壳基岩面起伏相对较小，风化残积形成的土壤分布也相对均匀。因此，白云岩区地表土层较厚，石漠化程度也稍弱于灰岩区。 相似文献
18.
Effect of the addition of granitic powder to an acidic soil from Galicia (NW Spain) in comparison with lime 总被引：1，自引：1，他引：0
The impact of diffuse pollution, agricultural land use and climate change on the long-term response of subsurface–surface water quality is not well understood, but is a prerequisite for evaluation of water management options. The goal of this study is to model geochemical evolution of water chemistry from the infiltration through soil into the unsaturated zone, transport through bedrocks and granular aquifers to a river in order to identify zones of steep concentration gradients and high dynamics under transient flow conditions. A numerical model was constructed comprising a 2-D 1,500 m × 150 m vertical cross-section of typical sedimentary rock formations, a glacio-fluvial quaternary gravel aquifer in the valley and soil layers. The model coupled saturated/un-saturated flow and reactive transport under steady state and transient conditions. Geochemical interactions, include intra-aqueous kinetic reactions of oxygen with dissolved organic matter, as well as kinetics of carbonate dissolution/precipitation. This model section was chosen to provide insight in to the principal processes and time scales affecting water chemistry along different flow paths. The numerical simulator MIN3P was used, a finite volume program for variably saturated subsurface flow and multi-component reactive transport. The results show that subsurface water residence times range from approximately 2 to 2,000 years. Different zones are to be expected with respect to the development of mineral equilibria; namely, purely atmospherically influenced, as well as open and closed system carbonate dissolution. Short-term responses to daily averaged changes in precipitation, however, are only visible to some extent in the shallower and near-river parts of flow system and solute loads. This can most likely be explained by directional changes in flow paths, indicating that equilibrium geochemical condition predominate at the hillslope scale, i.e. water quality depends on transport pathways rather than on kinetic effects. The extent of reducing conditions is controlled by the presence of organic-rich layers (i.e. peat deposits), the dissolution kinetics of aquifer organic matter and the subsequent mixing with oxygenated water by hydrodynamic dispersion. 相似文献
19.
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
20.
蚯蚓肠道内小分子有机酸与摄入的土壤矿物相互作用,加速矿物溶解。摄入的土壤在蚯蚓肠道内平均停留时间约为12 h,不足以使土壤矿物产生显著的溶解特征,因此这一过程难以在蚯蚓体内进行评估。本研究通过体外实验控制pH值和有机酸浓度,模拟蚯蚓肠道中有机酸对土壤中常见矿物的溶解反应,探讨了方解石和钾长石在蚯蚓肠道环境中的初始溶解动力学。研究发现,矿物在混合有机酸中的溶解速率比在纯水中高一个数量级,说明有机配体和质子促进了矿物溶解。溶解速率及粒度分析表明,方解石(CaCO3)溶解速率不受溶解过程中粒度变化的影响,而钾长石(KAlSi3O8)粒度在溶解期间未出现显著变化。在此基础上,采用初始速率法模拟了钾长石的初始溶解动力学,计算得出的溶解速率表明钾长石在溶解初期主要为表面K~+的释放。使用缩核模型(shrink core model)和Hixson-Crowell模型对方解石溶解过程进行动力学解析,发现方解石的溶解主要受溶液中反应物内扩散的速率影响。这定量描述了两种矿物在有机酸溶液和纯水中的溶解差异。现有研究表明,有机配体和质子协同促... 相似文献