Comparison of soil erosion and deposition rates using radiocesium, RUSLE, and buried soils in dolines in East Tennessee

 Three dolines (sinkholes), each representing different land uses (crop, grass, and forest) in a karst area in East Tennesse, were selected to determine soil erosional and depositional rates. Three methods were used to estimate the rates: fallout radiocesium (¹³⁷Cs) redistribution, buried surface soil horizons (Ab horizon), and the revised universal soil loss equation (RUSLE). When ¹³⁷Cs redistribution was examined, the average soil erosion rates were calculated to be 27 t ha^–1 yr^–1 at the cropland, 3 t ha^–1 yr^–1 at the grassland, and 2 t ha^–1 yr^–1 at the forest. By comparison, cropland erosion rate of 2.6 t ha^–1 yr^–1, a grassland rate of 0.6 t ha^–1 yr^–1, and a forest rate of 0.2 t ha^–1 yr^–1 were estimated by RUSLE. The ¹³⁷Cs method expressed higher rates than RUSLE because RUSLE tends to overestimate low erosion rates and does not account for deposition. The buried surface horizons method resulted in deposition rates that were 8 t ha^–1 yr^–1 (during 480 yr) at the cropland, 12 t ha^–1 yr^–1 (during 980 yr) at the grassland, and 4 t ha^–1 yr^–1 (during 101 yr) at the forest site. By examining ¹³⁷Cs redistribution, soil deposition rates were found to be 23 t ha^–1 yr^–1 at the cropland, 20 t ha^–1 yr^–1 at the grassland, and 16 t ha^–1 yr^–1 at the forest site. The variability in deposition rates was accounted for by temporal differences;¹³⁷Cs expressed deposition during the last 38 yr, whereas Ab horizons represented deposition during hundreds of years. In most cases, land use affected both erosion and deposition rates – the highest rates of soil redistribution usually representing the cropland and the lowest, the forest. When this was not true, differences in the rates were attributed to differences in the size, shape, and closure of the dolines. Received: 10 October 1995 · Accepted: 13 October 1995     

Carbonate and silicate weathering in two presently glaciated, crystalline catchments in the Swiss Alps

We present a weathering mass balance of the presently glaciated Rhône and Oberaar catchments, located within the crystalline Aar massif (central Switzerland). Annual chemical and physical weathering fluxes are calculated from the monthly weighted means of meltwater samples taken from July, 1999 to May, 2001 and are corrected for precipitation inputs. The meltwater composition issuing from the Oberaar and Rhône catchments is dominated by calcium, which represents 81% and 55% of the total cation flux respectively (i.e. 555 and 82-96 keq km⁻² yr⁻¹). The six to seven times higher Ca²⁺ denudation flux from the Oberaar catchment is attributed to the presence of a strongly foliated gneissic zone. The gneissic zone has an elevated calcite content (as reflected by the 4.6 times higher calcite content of the suspended sediments from Oberaar compared to Rhône) and a higher mechanical erosion rate (resulting in a higher flux of suspended sediment). The mean flux of suspended calcite of the Oberaar meltwaters during the ablation period is 7 times greater than that of the Rhône meltwaters. Taking the suspended calcite as a proxy for the total (including sub-glacial sediments) weathering calcite surface area, it appears that the available surface area is an important factor in controlling weathering rates. However, we also observe an increased supply of protons for carbonate dissolution in the Oberaar catchment, where the sulphate denudation flux is six times greater. Carbonic acid is the second important source of protons, and we calculate that three times as much atmospheric CO₂ is drawn down (short term) in the Oberaar catchment. Silica fluxes from the two catchments are comparable with each other, but are 100 kmol km² yr⁻¹ lower than fluxes from physically comparable, non-glaciated basins.     

Geospatial assessment of soil erosion vulnerability at watershed level in some sections of the Upper Subarnarekha river basin, Jharkhand, India

Undulating landscapes of Chhotanagpur plateau of the Indian state of Jharkhand suffer from soil erosion vulnerability of varying degrees. An investigation was undertaken in some sections of the Upper Subarnarekha River Basin falling within this state. An empirical equation known as Universal Soil Loss Equation (USLE) was utilized for estimating the soil loss. Analysis of remote sensing satellite data, digital elevation model (DEM) and geographical information system (GIS)–based geospatial approach together with USLE led to the soil erosion assessment. Erosion vulnerability assessment was performed by analyzing raster grids of topography acquired from Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) Global DEM data. LANDSAT TM and ETM+ satellite data of March 2001 and March 2011 were used for inferring the land use–land cover characteristics of the watershed for these years, respectively. USLE equation was computed within the GIS framework to derive annual soil erosion rates and also the areas with varying degrees of erosion vulnerability. Erosion vulnerability units thus identified covered five severity classes of erosion ranging from very low (0–5 ton ha^?1 yr^?1) to very severe (> 40 ton ha^?1 yr^?1). Results indicated an overall increase of erosion in the year 2011 as compared to the erosion computed for the year 2001. Maximum soil erosion rate during the year 2001 was found up to 40 ton ha^?1 yr^?1, whereas this went up to 49.80 ton ha^?1 yr^?1 for the year 2011. Factors for the increase in overall erosion could be variation in rainfall, decrease in vegetation or protective land covers and most important but not limited to the increase in built-up or impervious areas as well.     

Weathering fluxes of arsenic from a small catchment in Slovak Republic

Inputs of As to a small catchment due to chemical weathering of bedrock, mechanical weathering of bedrock, and atmospheric precipitation were 71.53, 23.98 and 0.02 g ha⁻¹ year⁻¹, respectively. The output fluxes of As due to mechanical erosion of soil, biological uptake, stream discharge, and groundwater flow were 6.32, 4.77, 0.37 and 0.02 g ha⁻¹ year⁻¹, respectively. The results indicate that arsenic accumulates in soil and regolith with a very high rate. This is attributed to the selective weathering and erosion with respect to arsenic and fixation of arsenic in the secondary solids produced by weathering. The output fluxes of As in stream and groundwater in Vydrica catchment in Slovak Republic (0.39 g ha⁻¹ year⁻¹) based on muscovite–biotite granites and granodiorites were much lower compared to catchments in a gold district in the Czech Republic. These results may be ascribed to the low levels of arsenic pollution measured in Vydrica catchment. The arsenic fluxes were estimated by calculation of mechanical and chemical weathering rates of the bedrocks in Vydrica catchment from mass balance data on sodium and silica. The justification of the steady state of Na and Si is that neither of the elements is appreciably accumulated in plants and in exchangeable pool of ions in soil.     

Relationship of environmental geochemistry to soil degradation in Helwan catchment, Egypt

Environmental geochemistry plays an important role in understanding the distribution of major cations (Ca²⁺, Mg²⁺, Na⁺, K⁺) in Helwan catchment, south Cairo, Egypt. Evaluation of soil mechanical erosion rate, depletion rate, exchangeable rates of base cations and sodium adsorption ratios are essential for understanding soil degradation problems in the representative Helwan catchment. Soil erosion is a natural process. It often becomes a problem when human activity causes it to occur much faster than under natural conditions. The results of the mechanical erosion rate of soil and the exchangeable rates of base cations are 1845 and 80.3 kg ha⁻¹ yr⁻¹, respectively. The high intensity of the mechanical erosion rate is probably attributed to the high specific surface area of the studied type of Vertisol, intensive application of fertilizer and industrial activities. Mechanical erosion of soil, exchangeable rate of base cations and the depletion rate of base cations are almost inexhaustible sources of sodium, and all these increase the problem of sodic soils and may affect plant productivity in Helwan catchment.     

Modeling Biogeochemistry,the Key for Understanding Environmental Chemistry of a Semi－Arid Soil in Egypt

1IntroductionThecomponentsoftheenvironmentaredamagedbyagriculturalpractices.Soilslosstheirfer tilityandwaterdeterioratesduetopollution .Chemicalweatheringofmineralandsoiloccursattheinterfacesbetweentheliquidandsolidphases;consequentlythesurfaceareaandcompositionofthemineralsplayanimportantroleinthisprocess.GarrelsandMackenzie ( 1 96 7)suggestedthatincon gruentweatheringreactionswouldproducedissolvedspeciesandnewsolidsthataremorestableintheweatheringenvironmentthantheoriginalbedrockminerals.Ro…     

Behavior of REE Fractionation during Weathering of Dolomite Regolith Profile in Southwest China

<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.     

Geochemistry of organic-rich river waters in Amazonia: Insights on weathering processes of intertropical cratonic terrain

In this study, eight organic-rich rivers that flow through the Brazilian craton in the southwestern Amazon rainforest are investigated. This investigation is the first of its type in this area and focuses on the effects of lithology, long-term weathering, thick soils, forest cover and hydrological period on the dissolved load compositions in rivers draining cratonic terrain. The major dissolved ion concentrations, alkalinity (TAlk), SiO₂, trace element concentrations, and Sr isotope contents in the water were determined between April 2009 and January 2010. In addition, the isotopic values of oxygen and hydrogen were determined between 2011 and 2013. Overall, the river water is highly dilute and dominated by the major dissolved elements TAlk, SiO₂ and K⁺ and the major dissolved trace elements Al, Fe, Ba, Mn, P, Zn and Sr, which exhibit large temporal and spatial variability and are closely correlated with the silicatic bedrock and hydrology. Additionally, rainwater and recycled water vapor and the size of the basin contribute to the geochemistry of the waters. The total weathering flux estimated from our results is 2–4 t km⁻².yr⁻¹, which is one of the lowest fluxes in the world. The CO₂ consumption rate is approximately 21–61 10³ mol km⁻² yr⁻¹, which is higher than expected given the stability of the felsic to basic igneous and metamorphic to siliciclastic basement rocks and the thick tropical soil cover. Thus, weathering of the cratonic terrain under intertropical humid conditions is still an important consumer of CO₂.     

Tolerable versus actual soil erosion rates in Europe

Erosion is a major threat to soil resources in Europe, and may impair their ability to deliver a range of ecosystem goods and services. This is reflected by the European Commission's Thematic Strategy for Soil Protection, which recommends an indicator-based approach for monitoring soil erosion. Defined baseline and threshold values are essential for the evaluation of soil monitoring data. Therefore, accurate spatial data on both soil loss and soil genesis are required, especially in the light of predicted changes in climate patterns, notably frequency, seasonal distribution and intensity of precipitation. Rates of soil loss are reported that have been measured, modelled or inferred for most types of soil erosion in a variety of landscapes, by studies across the spectrum of the Earth sciences. Natural rates of soil formation can be used as a basis for setting tolerable soil erosion rates, with soil formation consisting of mineral weathering as well as dust deposition. This paper reviews the concept of tolerable soil erosion and summarises current knowledge on rates of soil formation, which are then compared to rates of soil erosion by known erosion types, for assessment of soil erosion monitoring at the European scale.A modified definition of tolerable soil erosion is proposed as ‘any actual soil erosion rate at which a deterioration or loss of one or more soil functions does not occur,’ actual soil erosion being ‘the total amount of soil lost by all recognised erosion types.’ Even when including dust deposition in soil formation rates, the upper limit of tolerable soil erosion, as equal to soil formation, is ca. 1.4 t ha^− 1 yr^− 1 while the lower limit is ca. 0.3 t ha^− 1 yr^− 1, for conditions prevalent in Europe. Scope for spatio-temporal differentiation of tolerable soil erosion rates below this upper limit is suggested by considering (components of) relevant soil functions. Reported rates of actual soil erosion vary much more than those for soil formation. Actual soil erosion rates for tilled, arable land in Europe are, on average, 3 to 40 times greater than the upper limit of tolerable soil erosion, accepting substantial spatio-temporal variation. This paper comprehensively reviews tolerable and actual soil erosion in Europe and highlights the scientific areas where more research is needed for successful implementation of an effective European soil monitoring system.     

Influence of landscape position and vegetation on long-term weathering rates at the Hubbard Brook Experimental Forest, New Hampshire, USA

The spatial variability of long-term chemical weathering in a small watershed was examined to determine the effect of landscape position and vegetation. We sampled soils from forty-five soil pits within an 11.8-hectare watershed at the Hubbard Brook Experimental Forest, New Hampshire. The soil parent material is a relatively homogeneous glacial till deposited ∼14,000 years ago and is derived predominantly from granodiorite and pelitic schist. Conifers are abundant in the upper third of the watershed while the remaining portion is dominated by hardwoods. The average long-term chemical weathering rate in the watershed, calculated by the loss of base cations integrated over the soil profile, is 35 meq m⁻² yr⁻¹—similar to rates in other ∼10 to 15 ka old soils developed on granitic till in temperate climates. The present-day loss of base cations from the watershed, calculated by watershed mass balance, exceeds the long-term weathering rate, suggesting that the pool of exchangeable base cations in the soil is being diminished. Despite the homogeneity of the soil parent material in the watershed, long-term weathering rates decrease by a factor of two over a 260 m decrease in elevation. Estimated weathering rates of plagioclase, potassium feldspar and apatite are greater in the upper part of the watershed where conifers are abundant and glacial till is thin. The intra-watershed variability across this small area demonstrates the need for extensive sampling to obtain accurate watershed-wide estimates of long-term weathering rates.     

Rates of Biotite Weathering,and Clay Mineral Transformation and Neoformation,Determined from Watershed Geochemical Mass-Balance Methods for the Coweeta Hydrologic Laboratory,Southern Blue Ridge Mountains,North Carolina,USA

Biotite is a common constituent of silicate bedrock. Its weathering releases plant nutrients and consumes atmospheric CO₂. Because of its stoichiometric relationship with its transformational weathering product and sensitivity to botanical activity, calculating biotite weathering rates using watershed mass-balance methods has proven challenging. At Coweeta Hydrologic Laboratory the coupling of biotite to its transformational weathering product is only valid if the stoichiometric relationship for the two phases is known; this relationship is unlikely layer-for-layer. Rates of biotite weathering and transformation of its secondary weathering product at the Coweeta Hydrological Laboratory are comparable with other Appalachian watersheds. The magnitude and sign of the difference between field- and laboratory-determined biotite weathering rates are similar to those of other silicate minerals. The influence of major-cation proportions in biomass on the rates of biotite weathering and transformational weathering product is greatest for watersheds with high biomass aggradation rates. The watershed with the lowest bedrock reactivity and highest flushing rate yielded the highest gibbsite formation rate of ~500 mol ha^?1 year^?1 and lowest kaolin-group mineral formation rates of 4–78 mol ha^?1 year^?1. The kaolin-group mineral formation rate increases as bedrock reactivity increases and flushing rate decreases to a maximum of ~300 mol ha^?1 year^?1, with a similar minimum gibbsite formation rate. The relative differences in bedrock reactivity and flux of water through Coweeta Hydrological Laboratory watersheds studied appear to be invariant over geologic timescales.     

Geochemistry of major and trace elements and Pb–Sr isotopes of a weathering profile developed on the Lower Cambrian black shales in central Hunan,China

This paper reports a geochemical study on the major and trace elements and Pb–Sr isotopes of a weathering profile developed in the Lower Cambrian black shales in central Hunan (China). Six weathering horizons were identified and sampled vertically throughout the profile. The chemical composition of the profile consists of variable concentrations of the major elements Fe₂O₃, FeO, MnO, MgO, CaO, Na₂O, and P₂O₅ and of less variable concentrations of SiO₂, TiO₂, Al₂O₃, and K₂O. The chemical change caused by weathering is estimated by mass-balance calculations, and the results show that the element mobility is characterised by substantial loss of SiO₂, FeO, CaO, K₂O, Na₂O, LOI, Cr, V, Ba, Cs, Rb, Sr, U, and Th, and moderate loss of Al₂O₃, MgO, Fe₂O₃, Ni, Cu, Pb, Tl, Sn, Sc, Ge and REE (Y). The high field strength elements TiO₂, Sn, Sc, U, Ga, Ge, Zr, Hf, Nb, and Ta were immobile during weathering. The chemical changes and the Pb–Sr isotopic data suggest that four types of chemical reactions occurred: the oxidation of sulphide minerals (e.g., pyrite) and organic carbon (OS), the dissolution of less resistant clinochlore-Ia, calcite, and P-bearing minerals (DL), the dissolution of detrital albite and microcline (DA), and the transformation of clay (TC) minerals (e.g., muscovite and illite–smectite). These chemical reactions then led to two stages of geochemical processes, an early stage of chemical differentiation and a later stage of chemical homogenisation. The chemical differentiation dominated by the OS, DL, and DA reactions, led to the leaching of mobile elements (e.g., MgO, Na₂O, K₂O, P₂O₅, Sr, and REE) and the redistribution of some less mobile elements (e.g., SiO₂ and Al₂O₃). In contrast, the chemical homogenisation, which was caused by TC reactions, led to the leaching of both mobile and less mobile elements from the system and ultimately transformed the weathered black shales into soil. Soils derived from black shales in South China might result from the above two geochemical processes.     

Modeling of subsurface calcite dissolution, including the respiration and reoxidation processes of marine sediments in the region of equatorial upwelling off Gabon

Mineralization of organic matter and the subsequent dissolution of calcite were simulated for surface sediments of the upper continental slope off Gabon by using microsensors to measure O₂, pH, pCO₂ and Ca²⁺ (in situ), pore-water concentration profiles of NO₃⁻, NH₄⁺, Fe²⁺, and Mn²⁺ and SO₄²⁻ (ex situ), as well as sulfate reduction rates derived from incubation experiments. The transport and reaction model CoTReM was used to simulate the degradation of organic matter by O₂, NO₃⁻, Fe(OH)₃ and SO₄²⁻, reoxidation reactions involving Fe²⁺ and Mn²⁺, and precipitation of FeS. Model application revealed an overall rate of organic matter mineralization amounting to 50 μmol C cm⁻² yr⁻¹, of which 77% were due to O₂, 17% to NO₃⁻ and 3% to Fe(OH)₃ and 3% to SO₄²⁻. The best fit for the pH profile was achieved by adapting three different dissolution rate constants of calcite ranging between 0.01 and 0.5% d⁻¹ and accounting for different calcite phases in the sediment. A reaction order of 4.5 was assumed in the kinetic rate law. A CaCO₃ flux to the sediment was estimated to occur at a rate of 42 g m⁻² yr⁻¹ in the area of equatorial upwelling. The model predicts a redissolution flux of calcite amounting to 36 g m⁻² yr⁻¹, thus indicating that ∼90% of the calcite flux to the sediment is redissolved.     

Organic carbon stocks and erosion in the soils of Guangdong,South China

Soil organic carbon (SOC) storage and erosion in South China at the regional scale in the past decades remains far from being understood. This paper calculated the SOC density, storage and erosion in 14 soil classes in Guangdong Province, South China, based on statistical data from the soil survey and soil erosion survey of Guangdong, which was performed in the 1990s. The purpose of this study is to understand the relationships between soil classes and SOC erosion at the regional scale. The results indicated that the SOC density in the soils of Guangdong varied from 12.7 to 144.9 Mg ha^?1 over the entire profile and from 12.6 to 68.4 Mg ha^?1 in the top 20-cm soil layer. The average area-weighted SOC density in the topsoil (0–20 cm) and the entire profile was 32 ± 3 and 86 ± 4 Mg ha^?1, respectively. The total SOC storage was 1.27 ± 0.06 Pg, with 35.6 % (0.46 ± 0.04 Pg) located in the topsoil. The average area-weighted strength of the SOC erosion in the 1990s was 20.6 ± 0.8 Mg km^?2 year^?1. The results indicated that SOC erosion was strongly related to soil class.     

Major ion chemistry of the Yarlung Tsangpo-Brahmaputra river: Chemical weathering, erosion, and CO2 consumption in the southern Tibetan plateau and eastern syntaxis of the Himalaya

The Yarlung Tsangpo-Brahmaputra river drains a large portion of the Himalaya and southern Tibetan plateau, including the eastern Himalayan syntaxis, one of the most tectonically active regions on the globe. We measured the solute chemistry of 161 streams and major tributaries of the Tsangpo-Brahmaputra to examine the effect of tectonic, climatic, and geologic factors on chemical weathering rates. Specifically, we quantify chemical weathering fluxes and CO₂ consumption by silicate weathering in southern Tibet and the eastern syntaxis of the Himalaya, examine the major chemical weathering reactions in the tributaries of the Tsangpo-Brahmaputra, and determine the total weathering flux from carbonate and silicate weathering processes in this region. We show that high precipitation, rapid tectonic uplift, steep channel slopes, and high stream power generate high rates of chemical weathering in the eastern syntaxis. The total dissolved solids (TDS) flux from the this area is greater than 520 tons km⁻² yr⁻¹ and the silicate cation flux more than 34 tons km⁻² yr⁻¹. In total, chemical weathering in this area consumes 15.2 × 10⁵ mol CO₂ km⁻² yr⁻¹, which is twice the Brahmaputra average. These data show that 15-20% of the total CO₂ consumption by silicate weathering in the Brahmaputra catchment is derived from only 4% of the total land area of the basin. Hot springs and evaporite weathering provide significant contributions to dissolved Na⁺ and Cl⁻ fluxes throughout southern Tibet, comprising more than 50% of all Na⁺ in some stream systems. Carbonate weathering generates 80-90% of all dissolved Ca²⁺ and Mg²⁺ cations in much of the Yarlung Tsangpo catchment.     

GEOCARBSULF: A combined model for Phanerozoic atmospheric O2 and CO2

A model for the combined long-term cycles of carbon and sulfur has been constructed which combines all the factors modifying weathering and degassing of the GEOCARB III model [Berner R.A., Kothavala Z., 2001. GEOCARB III: a revised model of atmospheric CO₂ over Phanerozoic time. Am. J. Sci. 301, 182-204] for CO₂ with rapid recycling and oxygen dependent carbon and sulfur isotope fractionation of an isotope mass balance model for O₂ [Berner R.A., 2001. Modeling atmospheric O₂ over Phanerozoic time. Geochim. Cosmochim. Acta65, 685-694]. New isotopic data for both carbon and sulfur are used and new feedbacks are created by combining the models. Sensitivity analysis is done by determining (1) the effect on weathering rates of using rapid recycling (rapid recycling treats carbon and sulfur weathering in terms of young rapidly weathering rocks and older more slowly weathering rocks); (2) the effect on O₂ of using different initial starting conditions; (3) the effect on O₂ of using different data for carbon isotope fractionation during photosynthesis and alternative values of oceanic δ¹³C for the past 200 million years; (4) the effect on sulfur isotope fractionation and on O₂ of varying the size of O₂ feedback during sedimentary pyrite formation; (5) the effect on O₂ of varying the dependence of organic matter and pyrite weathering on tectonic uplift plus erosion, and the degree of exposure of coastal lands by sea level change; (6) the effect on CO₂ of adding the variability of volcanic rock weathering over time [Berner, R.A., 2006. Inclusion of the weathering of volcanic rocks in the GEOCARBSULF model. Am. J. Sci.306 (in press)]. Results show a similar trend of atmospheric CO₂ over the Phanerozoic to the results of GEOCARB III, but with some differences during the early Paleozoic and, for variable volcanic rock weathering, lower CO₂ values during the Mesozoic. Atmospheric oxygen shows a major broad late Paleozoic peak with a maximum value of about 30% O₂ in the Permian, a secondary less-broad peak centered near the Silurian/Devonian boundary, variation between 15% and 20% O₂ during the Cambrian and Ordovician, a very sharp drop from 30% to 15% O₂ at the Permo-Triassic boundary, and a more-or less continuous rise in O₂ from the late Triassic to the present.     

河北承德锗元素生态地球化学特征及其与道地药材黄芩适生关系

道地药材生长与生态地球化学研究对实现中医药科学化和标准化具有重要意义。从承德市滦河流域与金沟屯和五道岭典型研究区阐明区域尺度和不同地质建造区Ge元素地球化学背景特征,结合多元统计采用基于Nb元素的质量迁移系数、化学蚀变指数CIA和残积系数RF、生物富集系数论述Ge元素在基岩-风化壳-土壤-黄芩系统中的迁移聚集规律,探讨Ge元素生态地球化学特征与道地药材黄芩的适生关系。结果表明：滦河流域表层土壤Ge元素平均含量为1.336 mg·kg^-1,43.54%土壤样品Ge元素含量属丰富—较丰富水平;金沟屯和五道岭区表层土壤Ge元素平均含量分别为1.352 mg·kg^-1和1.268 mg·kg^-1。不同地质建造和表层土壤Ge元素含量与TFe₂O₃含量显著相关,土壤含铁矿物对Ge元素具有吸附作用。Ge元素含量随岩土风化程度升高而增大,金沟屯区土壤风化程度高于五道岭区,土壤成熟度相对较高,Ge元素富集程度相对较高。岩石风化过程中Ge元素与TFe₂O₃、V、Ti、Co、P、Pb、Cu、Zn、Al₂O₃、SiO₂、K₂O、Na₂O质量迁移系数值相近,风化土壤与新鲜基岩Si和Ge含量发生明显分异,Ge元素主要来源于硅酸盐矿物风化过程中晶格破裂和金属硫化物矿物风化释放。金沟屯和五道岭黄芩Ge元素BCF平均值分别为0.014和0.020,黄芩根部对土壤Fe与Ge的吸收表现出明显的协同作用,土壤pH影响着Ge元素形态和生物有效性。区域土壤丰富的Fe、P和Sr元素含量为优质黄芩生长提供了有利条件;Fe族元素含量丰富,pH呈微碱性的沙壤质土壤为道地药材黄芩适宜生长和定向栽培种植区。     

An assessment of soil erosion probability and erosion rate in a tropical mountainous watershed using remote sensing and GIS

Remote sensing data and Geographical Information System (GIS) has been integrated with the weighted index overlay (WIO) method and E ₃₀ model for the identification and delineation of soil erosion susceptibility zones and the assessment of rate of soil erosion in the mountainous sub-watershed of River Manimala in Kerala (India). Soil erosion is identified as the one of the most serious environmental problems in the human altered mountainous environment. The reliability of estimated soil erosion susceptibility and soil loss is based on how accurately the different factors were estimated or prepared. In the present analysis, factors that are considered to be influence the soil erosion are: land use/land cover, NDVI, landform, drainage density, drainage frequency, lineament frequency, slope, and relative relief. By the WIO analysis, the area is divided into zones representing low (33.30%), moderate (33.70%), and high (33%) erosion proneness. The annual soil erosion rate of the area under investigation was calculated by carefully determining its various parameters and erosion for each of the pixels were estimated individually. The spatial pattern thus created for the area indicates that the average annual rate of soil erosion in the area was ranging from 0.04 mm yr⁻¹ to 61.80 mm yr⁻¹. The high soil erosion probability and maximum erosion rate was observed in areas with high terrain alteration, high relief and slopes with the intensity and duration of heavy precipitation during the monsoons.     

Geochemistry applied to the watershed survey: hydrograph separation,erosion and soil dynamics. A case study: the basin of the Niger River,Africa

A periodic sampling (85 samples) collected fortnightly along 3 annual hydrological cycles (1990–1993) in the Niger River basin, at the outlet of Bamako (Mali), allowed the calibration of an hydrochemical model based on the hydrograph separation. As a first step, 5 reservoirs are identified: Rr the rapid runoff, Rs the superficial runoff, Rh the hypodermic or differred runoff, Ns the superficial ground water, and Np the deep ground water, also called base flow. In each reservoir, the physico-chemical composition of water is supposed to be constant with time. Along the hydrograph, or total discharge curves, and during 3 hydrological cycles, the relative proportions of each of the reservoirs fluctuate continuously. The methodology, processing step by step, is first calibrated, by using concentrations of specific tracers: dissolved Na⁺, HCO₃⁻, and suspended sediments (TSS). Then, the proportions of Rr, Rs, Rh, Ns, and Np, contributing to the total flow measured at each instant of sampling, are calculated. As a second step, pH and the concentrations of aqueous species (K⁺, Ca²⁺, Mg²⁺, Cl⁻, SO₄²⁻, DOC, SiO₂), are in turn calculated by regression analysis in each reservoir. Finally a test of validity of the method is presented as a very close correlation between measured and predicted fluctuating concentrations of each of the elements. From that satisfactory stage, the geochemical budget of weathering is conducted, with particular attention to SiO₂ release and CO₂ consumption. Parent-rock mineralogical compositions contributing to dissolved species in the total discharge as well as in the individual flow components have been reconstituted. Rates of both chemical erosion (soil profile formation by weathering), and mechanical erosion (soil profile and landscape denudation) have been evaluated. The methodology, successfully applied to the Niger basin, is proposed as a strategic tool for studying the watershed dynamics for any time and space scales. The model revealed its ability to extrapolate and predict the geochemical or the environmental behaviour of such basins, naturally submitted to large secular or annual, regular or even catastrophic climatic oscillations.     

Present-day oxidative subsidence of organic soils and mitigation in the Sacramento-San Joaquin Delta,California, USA

Subsidence of organic soils in the Sacramento-San Joaquin Delta threatens sustainability of the California (USA) water supply system and agriculture. Land-surface elevation data were collected to assess present-day subsidence rates and evaluate rice as a land use for subsidence mitigation. To depict Delta-wide present-day rates of subsidence, the previously developed SUBCALC model was refined and calibrated using recent data for CO₂ emissions and land-surface elevation changes measured at extensometers. Land-surface elevation change data were evaluated relative to indirect estimates of subsidence and accretion using carbon and nitrogen flux data for rice cultivation. Extensometer and leveling data demonstrate seasonal variations in land-surface elevations associated with groundwater-level fluctuations and inelastic subsidence rates of 0.5–0.8 cm yr^–1. Calibration of the SUBCALC model indicated accuracy of ±0.10 cm yr^–1 where depth to groundwater, soil organic matter content and temperature are known. Regional estimates of subsidence range from <0.3 to >1.8 cm yr^–1. The primary uncertainty is the distribution of soil organic matter content which results in spatial averaging in the mapping of subsidence rates. Analysis of leveling and extensometer data in rice fields resulted in an estimated accretion rate of 0.02–0.8 cm yr^–1. These values generally agreed with indirect estimates based on carbon fluxes and nitrogen mineralization, thus preliminarily demonstrating that rice will stop or greatly reduce subsidence. Areas below elevations of –2 m are candidate areas for implementation of mitigation measures such as rice because there is active subsidence occurring at rates greater than 0.4 cm yr^–1.