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1.
In regolith-dominated terrains, the nature of contemporary processes and the surface distribution of regolith materials may be a poor guide to the character and history of regolith materials at depth. The nature of regolith materials at depth is often critical to unravelling the development of a landscape. Conventional mapping aids such as air photos, multispectral remote sensing and airborne radiometrics are not wholly adequate in this context, as they penetrate limited depths (<0.4 m). Airborne electromagnetics (AEM) on the other hand, has the potential to map regolith materials to considerable depths (>100m).The application of AEM to regolith mapping and its potential as a tool in geomorphology are illustrated by reference to an AEM survey flown at Lawlers in the Yilgarn Craton of Western Australia. At Lawlers, AEM identifies a palaeochannel that has no surface expression. It cannot be seen in images of the Landsat, airborne radiometric or airborne magnetic data. The disposition of this channel in the landscape, and in particular its association with ferruginous materials forming breakaways, suggest that inversion of relief has been a significant factor in the evolution of the Lawlers landscape.The AEM data at Lawlers have also been used to map the weathering front. The topography of the weathering front not only reflects the movement of water through the landscape in a general sense, but also reflects the influence of lithology and structure. Different lithologies are clearly weathering to different depths. Information on the nature of the weathering front is potentially an important constraint on models of groundwater flow, and by association, models of solute dispersion.  相似文献   

2.
Art F. White   《Chemical Geology》2002,190(1-4):69-89
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   


3.
Understanding the interactions of climate, physical erosion, chemical weathering and pedogenic processes is essential when considering the evolution of critical zone systems. Interactions among these components are particularly important to predicting how semiarid landscapes will respond to forecasted changes in precipitation and temperature under future climate change. The primary goal of this study was to understand how climate and landscape structure interact to control chemical denudation and mineral transformation across a range of semiarid ecosystems in southern Arizona. The research was conducted along the steep environmental gradient encompassed by the Santa Catalina Mountains Critical Zone Observatory (SCM-CZO). The gradient is dominated by granitic parent materials and spans significant range in both mean annual temperature (>10 °C) and precipitation (>50 cm a?1), with concomitant shift in vegetation communities from desert scrub to mixed conifer forest. Regolith profiles were sampled from divergent and convergent landscape positions in five different ecosystems to quantify how climate-landscape position interactions control regolith development. Regolith development was quantified as depth to paralithic contact and degree of chemical weathering and mineral transformation using a combination of quantitative and semi-quantitative X-ray diffraction (XRD) analyses of bulk soils and specific particle size classes. Depth to paralithic contact was found to increase systematically with elevation for divergent positions at approximately 28 cm per 1000 m elevation, but varied inconsistently for convergent positions. The relative differences in depth between convergent and divergent landscape positions was greatest at the low and high elevation sites and is hypothesized to be a product of changes in physical erosion rates across the gradient. Quartz/Plagioclase (Q/P) ratios were used as a general proxy for bulk regolith chemical denudation. Q/P was generally higher in divergent landscape positions compared to the adjacent convergent hollows. Convergent landscape positions appear to be collecting solute-rich soil–waters from divergent positions thereby inhibiting chemical denudation. Clay mineral assemblage of the low elevation sites was dominated by smectite and partially dehydrated halloysite whereas vermiculite and kaolinite were predominant in the high elevation sites. The increased depth to paralithic contact, chemical denudation and mineral transformation are likely functions of greater water availability and increased primary productivity. Landscape position within a given ecosystem exerts strong control on chemical denudation as a result of the redistribution of water and solutes across the landscape surface. The combined data from this research demonstrates a strong interactive control of climate, landscape position and erosion on the development of soil and regolith.  相似文献   

4.
《Chemical Geology》2004,203(1-2):29-50
The aim of this study is to characterize the evolution of the rare earth elements (REE) in the Pingba red residua on karst terrain of Yunnan-Guizhou Plateau. The in-situ weathering and the two-stage development of the profile had been inferred from REE criterions. The REE were significantly fractionated, and Ce was less mobilized and separated from the other REEs at the highly enriched top of the profile. This is consistent with the increase of oxidation degree in the regolith. And it is also suggested that the wet/dry climate change during chemical weathering caused Ce alternative change between enrichment and invariance in the upper regolith. Chondrite-normalized REE distribution patterns for samples from dolomites and the lower regolith are characteristic of MREE enrichment and remarkable negative Ce-anomalies patterns (similar to the convex-up REE patterns). The following processes are interpreted for the patterns in this study: (1) the accumulation of MRRE-rich minerals in dolomite dissolution, (2) water–rock interaction in the weathering front, and (3) more leaching MREE from the upper part of the profile. The latter two explanations are considered as the dominant process for the formation of the REE patterns. Samples from the soil horizon exhibit typical REE distribution patterns of the upper crust, i.e., LaN/YbN=10 and Eu/Eu*=0.65. All data indicate that the leaching process is very important for pedogenesis in this region. The experiments demonstrating that abnormal enrichment of REE at the upper regolith–bedrock interface is caused by a combination of volume change, accumulation of REE-bearing minerals, leaching of REE from the upper regolith, and water–rock interaction during rock–soil alteration processes. Our results support the conclusion that the weathering profile represents a large, continental elemental storage reservoir, whereas REE enrichment occurs under favorable conditions in terms of stable tectonics, low erosion and rapid weathering over sufficiently long time.  相似文献   

5.
The interface where bedrock transforms to regolith is not planar but rather has a roughness that varies with the scale of observation. The complexity of this surface is manifested in both element-depth and fragment size-depth distributions and may sometimes be related to the longitudinal profiles of watershed streams. The fractal nature of the bedrock-regolith interface means that the interface has a “thickness” which is >20 m in two ridgetop examples from Pennsylvania and Puerto Rico. Such weathering thicknesses, modeled as a function of one-dimensional fluid flow, are affected by the balance between rates of weathering and erosion. One-dimensional models are consistent with weathering advance rates that vary with equilibrium solubility and porefluid velocities (and not reaction kinetics). However, fluid flow is not strictly downward and one-dimensional. Permeability of regolith changes as particle size and bulk density changes with depth. Thus, both downward and lateral flow occurs especially at reaction fronts where reactions change permeability. The rate of weathering advance is, therefore, affected by the 3-dimensional distribution of reaction zones that affect permeability across the watershed. Quantitative models of such phenomena over a range of spatial and temporal scales are needed.  相似文献   

6.
Major and trace element concentrations were measured in bedrock, regolith and stream sediments from a first-order catchment developed entirely on grey shale in central Pennsylvania, USA. These elements can be classified into five major groups based on statistical data analysis. The presence of different elemental groups is due to the mineralogical origin, cycling processes, and geochemical properties of these elements during soil formation. A better understanding of the behaviors of these elements during chemical weathering would allow for their possible use as natural tracers in Critical Zone processes.  相似文献   

7.
《Applied Geochemistry》2002,17(3):321-336
Mineralogical, petrographical, and geochemical studies of the weathering profile have been carried out at Omai Au mine, Guyana. The area is underlain by felsic to mafic volcanic and sedimentary rocks of the Barama-Mazaruni Supergroup, part of the Paleoproterozoic greenstone belts of the Guiana Shield. Tropical rainy climate has favoured extensive lateritization processes and formation of a deeply weathered regolith. The top of the weathering profile consists of lateritic gravel or is masked by the Pleistocene continental-deltaic Berbice Formation. Mineralogical composition of regolith consists mainly of kaolinite, goethite and quartz, and subordinately sericite, feldspar, hematite, pyrite, smectite, heavy minerals, and uncommon mineral phases (nacrite, ephesite, corrensite, guyanaite). A specific feature of the weathering profile at Omai is the preservation of fresh hydrothermal pyrite in the saprolith horizon. Chemical changes during the weathering processes depend on various physicochemical and structural parameters. Consequently, the depth should not be the principal criterion for comparison purposes of the geochemical behavior within the weathering profile, but rather an index that measures the degree of supergene alteration that has affected each analyzed sample, independently of the depth of sampling. Thus, the mineralogical index of alteration (MIA) can provide more accurate information about the behavior of major and trace elements in regolith as opposed to unweathered bedrock. It can also aid in establishing a quantitative relationship between intensity of weathering and mobility (leaching or accumulation) of each element in each analyzed sample. At Omai, some major and trace elements that are commonly considered as immobile (ex: TiO2, Zr, etc.) during weathering could become mobile in several rock types and cannot be used to calculate the mass and volume balance. In addition, due to higher “immobile element” ratios, the weathered felsic volcanic rocks plotted in identification diagrams are shifted towards more mafic rock types and a negative adjustment of ∼20 units is necessary for correct classification. In contrast, these elements could aid in defining the material source in sedimentary rocks affected by weathering. Generally, the rare-earth element (REE) patterns of the bedrock are preserved in the saprolith horizon. This can represent a potentially useful tool for geochemical exploration in tropical terrains. Strong negative Ce and Tb anomalies are displayed by weathered pillowed andesites, which are explained by the influence of the water/rock ratio.  相似文献   

8.
Exploring the relationship between weathering and erosion is essential for understanding the evolution of landscapes and formation of soil under the influence of climate, tectonics, and topography. We measured the bulk chemistry of regoliths and calculated their weathering rates and intensity in three locations in China: Inner Mongolia in the mid-temperate semi-humid zone; Jiangxi Province, in the mid-subtropical humid zone; and Hainan Province, in the tropical humid zone. These profiles exhibited increased weathering with increasing temperature and precipitation. The low-gradient profile exhibited stronger weathering of saprolite than of soil, whereas the high-gradient profile showed a more constant weathering pattern. The regolith in the cold climate was the product of easily weatherable minerals, whereas weathering of K-feldspar and even secondary minerals occurred in hot and humid climates. The weathering of subtropical profiles was both supply- and kinetic-limited, controlled by weathering and erosion. The tropical profile experienced supply-limited weathering, indicating slow erosion and an intense weathering profile; the mid-temperate profile was not classifiable due to weak erosion and weathering. Long-term weathering fluxes of these profiles show that Si, Na, and K (or Mg) represent the bulk of the mass lost through weathering. This study underscores that weathering of granitic regolith is controlled by both climatic conditions and landscape.  相似文献   

9.
杨江海  马严 《地球科学》2017,42(11):1910-1921
源-汇沉积过程的实质是沉积物的产生、搬运和沉积.陆表岩石的风化、侵蚀是沉积物产生的主要过程,受气候和构造因素的联合控制.现代陆表风化层研究揭示,在特定风化机制下(供给限制型化学风化)表层土壤的化学风化强度主要与陆表温度和湿度(降雨量)有关,其关系可通过建立经验气候转换方程来描述.经源-汇过程,这些气候信息可随陆源碎屑沉积物从源到汇传递,并最终可能形成沉积记录而保存于地层序列中.由于源-汇系统的复杂性和自发波动性,气候信息传递受源区侵蚀和沉积路径等的影响和扰动,具有明显的选择性,其时效性与气候变化本身的幅度和频度有关.基于陆源碎屑沉积进行深时古气候研究需要加深对源-汇沉积过程的理解,并考虑沉积系统响应和可能气候变化的时间尺度.   相似文献   

10.
<正>REE fractionation during the weathering of dolomite has been recognized for decades.A regolith profile on dolomite in southwest Yunnan of China was selected to investigate the behaviors of REE during weathering.The weathering of dolomite is divided into two stages:the pedogenesis stage and soil evolution stage,corresponding to the saprolites and soils respectively in the regolith profile. SiO_2,TiO_2,P_2O_5,Zr,Hf,Nb and Ta were immobile components during the weathering by and large, while Al_2O_3,K_2O and Fe_2O_3 were lost during the soil evolution stage in the physical form(clay minerals probably).REE were fractionated during the whole weathering of dolomite.The field weathering profile and the lab acid-leaching experiments on dolomite indicate that MREE were enriched clearly relative to other REE during the pedogenesis stage in a "capillary ascending-adsorption" mechanism, but they did not fractionate clearly in the soil evolution stage.REE were lost and accumulated in the weathering front of dolomite during the soil evolution stage in a "physical-chemical leaching" mechanism.  相似文献   

11.
Weathering intensity changes due to climatic variability across tectonically stable portions of continental crust can generate a thick and extensive weathered cover, resulting in regolith-dominated terrains (RDTs). Mineral exploration in RDTs is challenging because of the lack of bedrock outcrop, and the difficulty of linking surface regolith geochemistry to the geology at depth. Complex weathering obscures the expression of the basement geochemistry in the regolith, and therefore the footprints of mineral systems are difficult to detect. The southeast of the Yilgarn Craton and the Albany–Fraser Orogen (AFO) in the south of Western Australia is an RDT that extends along the coastline and the Eucla basin.This study proposes a landscape evolution model of the AFO, driven by transgression–regression sea-level changes that resulted in the formation of numerous islands and development of estuarine zones. This model contrasts with the river system-dominated landscape evolution present in the Yilgarn Craton. This difference has significant implications for mineral exploration and geochemical interpretation of the regolith in this region.Weathering profiles developed “on inland” and “on island” are thicker and more mature than those developed in sea-inundated areas. Even if in the Yilgarn Craton local areas display reworking of weathering profiles and other complexities from Permian, non-marine Tertiary sediments and Quaternary fluvial and aeolian sediments, at a regional scale, if vertical geochemical mobility of elements has occurred, “on inland” and “on island” are more reliable for understanding geochemical anomaly-basement relationships, whereas the “marine inundated” areas require a more detailed investigation, because of the role of marine reworking of weathering profiles and possible mixture of sediments from different provenances.Landscape changes from the topographically high, dissected Yilgarn environment with thick saprolite development and uneven basement topography, to the nearly flat regions dominated by sand dunes and thin saprolite development at the coastline. These regions are the result of the erosional and depositional effects of successive sea-level transgression–regression cycles. Within this framework, the following four different regolith settings have been identified in a progressive change from Yilgarn Craton environments to the modern coastline: (1) Albany; (2) Kalgoorlie–Norseman; (3) Esperance; and (4) Neale.Mapping the palaeocoastlines, islands and estuarine zones, as well as the region of influence of marine limestones and sediments, can significantly improve the understanding of how surface geochemistry relates to the landscape, and how it links with the geology at depth, and therefore, how it may reflect the presence of mineral systems. Understanding the difference in the landscape evolution between the AFO and Yilgarn Craton is essential to properly calibrate mineral exploration protocols in both regions.  相似文献   

12.
Etch and intracutaneous landforms and their implications   总被引:1,自引:0,他引:1  

Many landforms, major and minor, and including plains of various types, inselbergs, boulders, flared slopes, Rillen and rock basins, are initiated beneath the land surface, at the weathering front. They have evolved in various lithological settings. Most are formed by differential moisture attack, either controlled, or strongly influenced, by bedrock structure. Such forms of subsurface derivation may be differentiated into etch or subcutaneous features that were initiated at the base of the regolith, and intracutaneous forms that had their origin within the weathering zone. Although the agent or agents responsible for eroding the regolith and exposing the bedrock forms have varied in space and time, the similarity of etch and intracutaneous forms is such that their basic morphology persists regardless of the climatic regime in which they now occur. As the regolith is widely developed on the land surface, the forms initiated beneath and within it cannot be taken as climatic indicators. Indeed, like structural forms, these convergent forms represent a varied but significant azonal element in the physiographic landscape.  相似文献   

13.
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   

14.
Early (>3 Gy) wetter climate conditions on Mars have been proposed, and it is thus likely that pedogenic processes have occurred there at some point in the past. Soil and rock chemistry of the Martian landing sites were evaluated to test the hypothesis that in situ aqueous alteration and downward movement of solutes have been among the processes that have transformed these portions of the Mars regolith. A geochemical mass balance shows that Martian soils at three landing sites have lost significant quantities of major rock-forming elements and have gained elements that are likely present as soluble ions. The loss of elements is interpreted to have occurred during an earlier stage(s) of weathering that may have been accompanied by the downward transport of weathering products, and the salts are interpreted to be emplaced later in a drier Mars history. Chemical differences exist among the sites, indicating regional differences in soil composition. Shallow soil profile excavations at Gusev crater are consistent with late stage downward migration of salts, implying the presence of small amounts of liquid water even in relatively recent Martian history. While the mechanisms for chemical weathering and salt additions on Mars remain unclear, the soil chemistry appears to record a decline in leaching efficiency. A deep sedimentary exposure at Endurance crater contains complex depth profiles of SO4, Cl, and Br, trends generally consistent with downward aqueous transport accompanied by drying. While no model for the origin of Martian soils can be fully constrained with the currently available data, a pedogenic origin is consistent with observed Martian geology and geochemistry, and provides a testable hypothesis that can be evaluated with present and future data from the Mars surface.  相似文献   

15.
Multiple Critical Zone Observatories (CZO) have been established in recent years in the USA and other international settings to conduct collaborative research on processes that occur at and near Earth’s surface, also known as the Critical Zone (CZ). Data documentation and data sharing are two persistent problems facing the CZOs that impede the ability for cross-site comparisons and integrated analysis. In this study, a relational database was developed for CZ rock and regolith geochemical data – CZChemDB. There are a total of 24 interrelated tables in the database, each representing different aspects of CZ features. The main data group includes tables of locations, sites, samples, subsamples, preparation/treatments, laboratory-analysis and data values. The meta-data group includes tables of methods, references, and data quality. Lookup tables (variables, units, etc.) contain lists of “controlled” vocabularies. The CZChemDB is currently implemented in the MS Access database management system. It is expected to be integrated into the EarthChem portal by summer of 2011 for broader online accessibility and usability. This integration also complements the EarthChem’s global geochemistry database with CZ regolith data. The structure of the CZChemDB is simple, straightforward, and flexible so that it has potential to accommodate other chemical data collected from CZOs, such as pore fluid data. Furthermore, the development of CZChemDB represents the first attempt toward the standardization of geochemical data documentation and data sharing among CZOs. This effort will establish a model to bridge the connections between data acquisition, data management, data sharing, and data searching/discovering that are all essential but weak in terms of linkages within most geoscience research projects.  相似文献   

16.
A technique for obtaining age estimates for regolith profiles in Australia, based on the oxygen‐isotope composition of the clay mineral assemblage in a profile, is applied to a variety of regolith profiles and kaolinitic sediments from across Australia. Excluding monsoonal regions in the north of the continent, it is possible to distinguish profiles formed in the Late Mesozoic‐Early Tertiary (δ18O values between +15 and +17.5%δō) from profiles formed in post‐mid‐Tertiary times (>+17.5%ō). In addition it is concluded that there remain widespread remnants of a deep‐weathered regolith which developed in pre‐Late Mesozoic (Early Cretaceous or Jurassic?) times when Australia was at high latitude. The low δ18O values associated with clays formed in pre‐Late Mesozoic times (+10 to +15%o) suggest that deep weathering took place in a cool to cold and presumably humid climate, contrary to the traditional belief that deep weathering requires tropical to subtropical temperatures. The formation of deep‐weathered profiles at high latitude in a comparatively cold climate may be linked in part to higher past atmospheric CO2 levels.  相似文献   

17.
Located in the uplands of the Valley and Ridge physiographic province of Pennsylvania, the Susquehanna/Shale Hills Critical Zone Observatory (SSHO) is a tectonically quiescent, first-order catchment developed on shales of the Silurian Rose Hill Formation. We used soil cores augered at the highest point of the watershed and along a subsurface water flowline on a planar hillslope to investigate mineral transformations and physical/chemical weathering fluxes. About 25 m of bedrock was also drilled to estimate parent composition. Depletion of carbonate at tens of meters of depth in bedrock may delineate a deep carbonate-weathering front. Overlying this, extending from ∼6 m below the bedrock-soil interface up into the soil, is the feldspar dissolution front. In the soils, depletion profiles for K, Mg, Si, Fe, and Al relative to the bedrock define the illite and chlorite reaction fronts. When combined with a cosmogenic nuclide-derived erosion rate on watershed sediments, these depletion profiles are consistent with dissolution rates that are several orders of magnitudes slower for chlorite (1-5 × 10−17 mol m−2 s−1) and illite (2-9 × 10−17 mol m−2 s−1) than observed in the laboratory. Mineral reactions result in formation of vermiculite, hydroxy-interlayered vermiculite, and minor kaolinite. During weathering, exchangeable divalent cations are replaced by Al as soil pH decreases.The losses of Mg and K in the soils occur largely as solute fluxes; in contrast, losses of Al and Fe are mostly as downslope transport of fine particles. Physical erosion of bulk soils also occurs: results from a steady-state model demonstrate that physical erosion accounts for about half of the total denudation at the ridgetop and midslope positions. Chemical weathering losses of Mg, Na, and K are higher in the upslope positions likely because of the higher degree of chemical undersaturation in porewaters. Chemical weathering slows down in the valley floor and Al and Si even show net accumulation. The simplest model for the hillslope that is consistent with all observations is a steady-state, clay weathering-limited system where soil production rates decrease with increasing soil thickness.  相似文献   

18.
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   

19.
Saprolite formation rates influence many important geological and environmental issues ranging from agricultural productivity to landscape evolution. Here we investigate the chemical and physical transformations that occur during weathering by studying small-scale “saprolites” in the form of weathering rinds, which form on rock in soil or saprolite and grow in thickness without physical disturbance with time. We compare detailed observations of weathered basalt clasts from a chronosequence of alluvial terraces in Costa Rica to diffusion-reaction simulations of rind formation using the fully coupled reactive transport model CrunchFlow. The four characteristic features of the weathered basalts which were specifically used as criteria for model comparisons include (1) the mineralogy of weathering products, (2) weathering rind thickness, (3) the coincidence of plagioclase and augite reaction fronts, and (4) the thickness of the zones of mineral reaction, i.e. reaction fronts. Four model scenarios were completed with varying levels of complexity and degrees of success in matching the observations. To fit the model to all four criteria, however, it was necessary to (1) treat diffusivity using a threshold in which it increased once porosity exceeded a critical value of 9%, and (2) treat mineral surface area as a fitting factor. This latter approach was presumably necessary because the mineral-water surface area of the connected (accessible) porosity in the Costa Rica samples is much less than the total porosity (Navarre-Sitchler et al., 2009). The model-fit surface area, here termed reacting surface area, was much smaller than the BET-measured surface area determined for powdered basaltic material. In the parent basalt, reacting surface area and diffusivity are low due to low pore connectivity, and early weathering is therefore transport controlled. However, as pore connectivity increases as a result of weathering, the reacting surface area and diffusivity also increase and weathering becomes controlled by mineral reaction kinetics. The transition point between transport and kinetic control appears to be related to a critical porosity (9%) at which pore connectivity is high enough to allow rapid transport. Based on these simulations, we argue that the rate of weathering front advance is controlled by the rate at which porosity is created in the weathering interface, and that this porosity increases because of mineral dissolution following a rate that is largely surface-reaction controlled.  相似文献   

20.
马晓晨  王家生  陈粲  王舟 《地球科学》2018,43(11):3853-3872
风化壳的元素地球化学组成可以反映风化壳的发育类型及其气候特征,地史时期形成的古风化壳的元素地球化学组成可以揭示古风化壳的类型及其古气候特征.华北地区新元古代晚期(景儿峪组)至寒武纪(府君山组)期间的地层记录缺乏连续性,广泛发育一套典型的古风化壳,该古风化壳的发育过程可能记录了晚新元古代至早寒武纪期间的古气候特点.针对华北房山地区景儿峪组顶部保存的古风化壳中常量元素的组成、元素迁移富集特征和风化系数等分布规律开展了较系统分析,结果表明:(1)SiO2、Al2O3、TFe2O3、CaO是景儿峪组顶部古风化壳的主要组分,Al2O3、TFe2O3、TiO2、K2O在风化壳的中上部相对富集,SiO2则轻微亏损,CaO、Na2O、MgO、P2O5被迁移淋失;(2)硅铝系数、硅铝铁系数、化学蚀变指数(CIA)、残积系数、风化淋溶系数(BA)等地球化学指标的垂向变化特征指示该古风化壳形成于温暖湿润条件下中等强度的化学风化作用,其风化过程可能经历了由较弱至较强再逐渐减弱的演变过程;(3)与现代发育于湖南、贵州、云南等地碳酸盐岩类基岩之上的风化壳元素地球化学特征对比,发现景儿峪组顶部古风化壳的Si淋失度和Fe、Al富集度均较低.综合研究区古风化壳的常量元素地球化学特征,同时结合新元古代晚期至寒武纪的华北板块古纬度迁移特征,认为房山地区景儿峪组顶部发育的古风化壳形成于温暖湿润的亚热带-热带气候,为脱硅富铝化程度较低的硅铝粘土型风化壳.   相似文献   

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