Silicate weathering of soil-mantled slopes in an active Alpine landscape

Despite being located on high, steep, actively uplifting, and formerly glaciated slopes of the Swiss Central Alps, soils in the upper Rhone Valley are depleted by up to 50% in cations relative to their parent bedrock. This depletion was determined by a mass loss balance based on Zr as a refractory element. Both Holocene weathering rates and physical erosion rates of these slopes are unexpectedly low, as measured by cosmogenic ¹⁰Be-derived denudation rates. Chemical depletion fractions, CDF, range from 0.12 to 0.48, while the average soil chemical weathering rate is 33 ± 15 t km⁻² yr⁻¹. Both the cosmogenic nuclide-derived denudation rates and model calculations suggest that these soils have reached a weathering steady-state since deglaciation 15 ky ago. The weathering signal varies with elevation and hillslope morphology. In addition, the chemical weathering rates decrease with elevation indicating that temperature may be a dominant controlling factor on weathering in these high Alpine basins. Model calculations suggest that chemical weathering rates are limited by reaction kinetics and not the supply rate of fresh material. We compare hillslope and catchment-wide weathering fluxes with modern stream cation flux, and show that high relief, bare-rock slopes exhibit much lower chemical weathering rates despite higher physical erosion rates. The low weathering fluxes from rocky, rapidly eroding slopes allow for the broader implication that mountain building, while elevating overall denudation rates, may not cause increased chemical weathering rates on hillslopes. In order for this sediment to be weathered, intermediate storage, for instance in floodplains, is required.     

Coal weathering and the geochemical carbon cycle

The weathering rate of sedimentary organic matter in the continental surficial environment is poorly constrained despite its importance to the geochemical carbon cycle. During this weathering, complete oxidation to carbon dioxide is normally assumed, but there is little proof that this actually occurs. Knowledge of the rate and mechanisms of sedimentary organic matter weathering is important because it is one of the major controls on atmospheric oxygen level through geologic time.We have determined the aqueous oxidation rates of pyrite-free bituminous coal at 24° and 50°C by using a dual-cell flow-through method. Coal was used as an example of sedimentary organic matter because of the difficulty in obtaining pyrite-free kerogen for laboratory study. The aqueous oxidation rate obtained in the present study for air-saturated water (270 μM O₂) was found to be on the order of 2 × 10⁻¹² mol O₂/m²/s at 25°C, which is fast compared to other geologic processes such as tectonic uplift and exposure through erosion. The reaction order with respect to oxygen level is 0.5 on a several thousand hour time scale for both 24° and 50°C experiments. Activation energies, determined under 24° and 50°C conditions, were ≈40 kJ/mol O₂ indicating that the oxidation reaction is surface reaction controlled.The oxygen consumption rate obtained in this study is two to three orders of magnitude smaller than that for pyrite oxidation in water, but still rapid on a geologic time scale. Aqueous coal oxidation results in the formation of dissolved CO₂, dissolved organic carbon (DOC), and solid oxidation products, which are all quantitatively significant reaction products.     

Identification of rock weathering and environmental control in arid catchments (northern Xinjiang) of Central Asia

Chemical weathering is an integral part of the earth surface processes, whose spatial patterns and controlling factors on continental scale are still not fully understood. Highlands of the Asian continent have been shown having some of the highest observed rates of chemical weathering yet reported. However, the paucity of river gauge data in many of these terrains has limited determination of chemical weathering budget in a continental scale. A dataset of three large watersheds throughout northern Xinjiang in Central Asia is used to empirically identify chemical weathering regimes and interpret the underlying controlling factors. Detailed analysis of major ion ratios and a forward model of mass budget procedure are presented to distinguish the relative significances and contributions of silicate, carbonate weathering and evaporite dissolution. The analytical results show that carbonic acid is the most important weathering agent to the studied watersheds. Silicate weathering contributes, on average, ∼17.8% (molar basis) of total cations on a basin wide scale with an order of Zhungarer > Erlqis > Yili, indicating that silicate weathering, however, does not seem to be intense in the study basins. Evaporite dissolution, carbonate weathering and precipitation input contribute 43.6%, 29.7% and 8.9% of the total dissolved cations on average for the whole catchment, respectively. The three main morphological and hydrological units are reflected in water chemistry. Rivers from the montane areas (recharge area) of the three watersheds are very dilute, dominated by carbonate and silicate weathering, whereas the rivers of piedmont areas as well as the rivers of the sedimentary platform (runoff area) are dominated by carbonate weathering, and rivers of desert plain in the central Zhungarer basin (discharge area) are dominated by evaporite dissolution and are SO₄ rich. This spatial pattern indicates that, beside lithology, runoff conditions have significant role on the regional chemical weathering regimes. Chemical weathering processes in the areas appear to be significantly climate controlled, displaying a tight correlation with runoff and aridity. Carbonate weathering are mostly influenced by runoff, which is higher in the mountainous part of the studied basins. The identification of chemical weathering regimes from our study confirmed the weathering potential and complexity of temperate watersheds in arid environment and that additional studies of these terrains are warranted. However, because the dominant weathering reactions in the sedimentary platform of northern Xinjiang are of carbonates and evaporites rather than silicate minerals, and the climatic factors have important role on the rock weathering regimes, we think that weathering at the arid temperate drainage system (Central Asia) is maybe not an important long-term sink for atmospheric CO₂, if the future climate has no great change.     

Bacterially-mediated weathering of crystalline and amorphous Cu-slags

Two types of Cu-slags (CS: crystalline massive slag and GS: granulated amorphous slag) exhibiting a different chemical and mineral phase composition were compared with respect to their susceptibility to bacterial weathering using Pseudomonas aeruginosa (n° CIP 105094). Abiotic conditions e.g. sterile growth medium and ultrapure water were used for comparison. The experiments were extended up to 112 days with a systematic liquid phase renewal every 14 days. The results revealed significant release of elements in the bacterially mediated weathering experiments. Concentrations of elements (Si, Fe, Cu, Zn and Pb) in the biotic solutions were increased at least by 20% up to 99% compared to abiotic ones. From 3 to 77% of the leached elements were associated to the fraction >0.22 μm. Scanning electron microscope observations demonstrated greater weathering of mineral phases in biotic experiments than in abiotic ones which is in accordance with the solution chemistry exhibiting higher concentrations of elements leached in biotic set-ups. In the case of CS, glass and sulfides weathering was yet observed in abiotic experiment, whereas partial dissolution of fayalite (Fe₂SiO₄) was solely affected by the presence of bacteria. GS having a higher bulk content of metallic elements was found to be more stable than sulfide-bearing CS, while its (GS) glass matrix was found to weather easier under biotic conditions.     

基于结构体的峨眉山玄武岩风化程度评价（Ⅳ）：风化指数FF

提要：岩石化学风化程度评价指标应该同时满足以下三个基本条件,即与风化程度之间的关系简单明确、对风化程度变化具有足够的敏感性和易于确定和不易受到人为因素影响。作为铁镁质岩石的主要代表,（峨眉山）玄武岩风化程度评价除考虑可引起组分淋失与富集的水解反应外,还应充分考虑二价铁的氧化反应。新鲜峨眉山玄武岩中并存的二价铁和三价铁的含量总体稳定,910个样品的FeO、Fe₂O₃平均含量分别为8.45%和5.15%,以均匀、随机的方式赋存于辉石、橄榄石、杏仁体中的绿泥石、磁铁矿及火山玻璃中。风化玄武岩、玄武岩斜坡地下水及新鲜玄武岩浸泡液的地球化学研究结果表明,FeO及Fe₂O₃含量对峨眉山玄武岩风化程度的敏感性明显高于其他组分,同时铁又是玄武岩风化过程中活动性最差的元素之一。三价铁和二价铁的摩尔数比值（FF）适合于峨眉山玄武岩整个风化过程的风化程度判别,比既有风化指数具有更高的分辨率,尤其是对风化初期玄武岩。     

Northern latitude chemical weathering rates: clues from the Mackenzie River Basin, Canada

The main scope of this study is to investigate parameters controlling chemical weathering rates for a large river system submitted to subarctic climate. More than 110 river water samples from the Mackenzie River system (northern Canada) have been sampled and analyzed for major and trace elements and Sr isotopic ratios in the dissolved phase. The three main morphological units are reflected in water chemistry. Rivers from the Canadian Shield are very dilute, dominated by silicate weathering (Millot et al., 2002), whereas the rivers of the Rocky and Mackenzie Mountains as well as the rivers of the sedimentary Interior Platform are dominated by carbonate weathering and are SO₄ rich. Compared to the rivers of the Mackenzie and Rocky Mountains, the rivers of the interior plains are organic, silica, and Na rich and constitute the dominant input term to the Mackenzie River mainstream. Rivers of the Canadian Shield area do not significantly contribute to the Mackenzie River system. Using elemental ratios and Sr isotopic ratios, a mathematical inversion procedure is presented that distinguishes between solutes derived from silicate weathering and solutes derived from carbonate weathering. Carbonate weathering rates are mostly controlled by runoff, which is higher in the mountainous part of the Mackenzie basin. These rates are comparable to the carbonate weathering rates of warmer areas of the world. It is possible that part of the carbonate weathering is controlled by sulfide oxidative weathering, but its extent remains difficult to assess. Conversely to what was stated by Edmond and Huh (1997), overall silicate weathering rates in the Mackenzie basin are low, ranging from 0.13 to 4.3 tons/km²/yr (Na + K + Ca + Mg), and confirm the negative action of temperature on silicate weathering rates for river basins in cold climates. In contrast to what has been observed in other large river systems such as the Amazon and Ganges Rivers, silicate weathering rates appear 3 to 4 times more elevated in the plains than in the mountainous headwaters. This contradicts the “Raymo hypothesis” (Raymo and Ruddiman, 1992). Isotopic characterization of suspended material clearly shows that the higher weathering rates reported for the plains are not due to the weathering of fine sediments produced in the mountains (e.g., by glaciers) and deposited in the plains. Rather, the relatively high chemical denudation rates in the plains are attributed to lithology (uncompacted shales), high mechanical denudation, and the abundance of soil organic matter derived from incomplete degradation and promoting crystal lattice degradation by element complexation. The three- to fourfold factor of chemical weathering enhancement between the plains and mountains is similar to the fourfold factor of enhancement found by Moulton et al. (2000) between unvegetated and vegetated watershed. This study confirms the negative action of temperature on silicate weathering for cold climate but shows that additional factors, such as organic matter, associated with northern watersheds are able to counteract the effect of temperature. This acceleration by a factor of 4 in the plains is equivalent to a 6°C increase in temperature.     

热带地区碳酸盐岩上覆红色风化壳的成因机理及元素演化

开展热带岩溶地区红色风化壳元素地球化学演化规律研究,有助于丰富碳酸盐岩风化成土理论的认识。在越南北部选取典型的碳酸盐岩风化剖面,分析热带气候条件下碳酸盐岩上覆红色风化壳中主量元素的物质来源和演化特征。结果表明:无论Ti/Zr的元素比值分析,Hf-Zr、Nb-Ta及Sm-Nd的元素对协变分析,还是上地壳元素平均值(UCC)标准化分析,两个剖面的上覆风化壳均显示原地残积的特征,即两个剖面是碳酸盐岩的原位风化产物。碳酸盐岩风化成土过程中,CaO、MgO淋失明显,Al_2O_3和Fe_2O_3发生富集,显示两个剖面均经历较强的风化过程,但是白云岩和灰岩剖面有一定的分异特征。越南北部白云岩风化剖面从基岩到上部土层显示出稳定的Ti-Fe元素共富集特征,而灰岩剖面中Fe的增长速率明显超过Ti。白云岩上覆风化壳经历了强烈的风化作用,其脱硅作用弱于灰岩风化剖面,而富集铝的作用强于灰岩。迁移系数的演化规律说明两个剖面中长石成分(钾长石、钠长石等)或次生矿物(伊利石等)在风化成土过程中逐渐分解,同时Al、Fe、Si等稳定元素的在风化剖面中不断富集。     

Chemical overprinting of magmatism by weathering: A practical method for evaluating the degree of chemical weathering of granitoids

Quantitative determination of the degree of chemical weathering of rocks is a fundamental task in environmental and engineering geology, and many weathering indices based on whole-rock chemistry have been proposed. However, most classical indices are of limited application to granitoids in a wide area, because these lithotypes generally exhibit wide chemical variation arising from their petrogenesis. The chemical evolution produced during rock weathering, therefore, overprints pre-existing magmatic chemical variation. This problem can cause many classical weathering indices to yield misleading results. This study proposes a method that compensates for the influence of petrogenesis on calculation of the weathering index. The method is based on a bivariate plot of the magmatic chemical variation (MCV) in granitoids, and the degree of chemical weathering (DCW). The MCV axis must be based on an element that reflects magmatic processes and is also relatively immobile during rock weathering. In this study TiO₂ contents are utilized for the MCV. The DCW axis is fundamentally defined by the ratios of more-mobile to less-mobile elements during weathering, and hence many classical indices can be applied. The improved value of the degree of chemical weathering (DCW_i) for a weathered rock is derived by:

DCWi=s×(MCVCV-MCV₁)+DCW₁${\text{DCW}}_{\text{i}}=\text{s}\times ({\text{MCV}}_{\text{CV}}-{\text{MCV}}_1)+{\text{DCW}}_1$

where MCV₁ is the measured composition (e.g. TiO₂ content) of the weathered rock. DCW₁ denotes the ratios of more-mobile to less-mobile elements of the weathered rock. The “s” parameter is the slope of the least square linear regression for fresh granitoids in the MCV–DCW relationship. MCV_CV is a correction factor which is given by the average point on the MCV axis (e.g. average TiO₂) of the fresh rocks. This method is useful for evaluating the degree of weathering of various granitoids, and enhances the practical application of many weathering indices.     

Volcanic and anthropogenic contributions to global weathering budgets

We evaluate whether the global weathering budget is near steady state for the pre-anthropogenic modern environment by assessing the magnitude of acidity-generating volcanic exhalations. The weathering rate induced by volcanic acid fluxes, of which the CO₂ flux is the most important, can be expressed as an average release rate of dissolved silica, based on a model feldspar-weathering scheme, and the ratio of carbonate-to-silicate rock weathering. The theoretically predicted flux of silica from chemical weathering is slightly smaller than the estimated global riverine silica flux. After adjustment for carbonate weathering, the riverine dissolved bicarbonate flux is larger than the volcanic carbon degassing rate by a factor of about three. There are substantial uncertainties associated with the calculated and observed flux values, but the modern system may either not be in steady state, or additional, “unknown” carbon sources may exist. The closure errors in the predicted budgets and observed riverine fluxes suggest that continental weathering rates might have had an impact on atmospheric CO₂ levels at a time scale of 10³-10⁴ years, and that enhanced weathering rates during glacial periods might have been a factor in the reduced glacial atmospheric CO₂ levels. Recent anthropogenic emissions of carbon and sulfur have a much larger acid-generating capacity than the natural fluxes. Estimated potential weathering budgets to neutralize these fluxes are far in excess of observed values. A theoretical scenario for a return to steady state at the current anthropogenic acidity emissions (disregarding the temporary buffering action of the ocean reservoir) requires either significantly lower pH values in continental surface waters as a result of storage of strong acids, and/or higher temperatures as a result of enhanced atmospheric CO₂ levels in order to create weathering rates that can neutralize the total flux of anthropogenic and natural background acidity.     

基于扫描电镜图像和微观渗流模型的云冈石窟砂岩风化特征分析

风化作用、岩石微观结构、岩石微观渗流特性定量关系的研究是石窟文物有效保护的重要基础,砂岩风化作用严重影响了岩体上石窟文物的有效保护。本次研究使用扫描电镜（SEM）获得云冈石窟不同窟体砂岩的微观图像,根据图像增强和图像分割技术得到了岩石中颗粒和孔隙的数字特征参数,从微观角度建立了反映孔喉连接特性的渗流模型,得到了不同窟体岩石的局部水力传导系数,分析了数字特征参数、水力传导系数、风化作用之间的关系。结果表明,风化作用对石窟砂岩微观结构具有很大影响;砂岩孔隙平均长轴长度大小对应的风化程度分别是全风化或强风化、中等风化、微风化或未风化,长度分别为大于40 μm、25～35 μm、15～25 μm;风化程度越高、水力传导系数越大,随着风化程度的增高、水力传导系数的范围为1 × 10?9～1 × 10?4 cm/s;水力传导系数与孔喉尺寸、孔喉连通性密切相关;孔喉半径比增大时、水力传导系数也增大。     

Mountain building-enhanced continental weathering and organic carbon burial as major causes for climatic cooling at the Frasnian–Famennian boundary (c. 376 Ma)?

The Late Devonian was a period of drastic environmental changes, as exemplified by a major biotic crisis at the Frasnian–Famennian boundary (FFB) and the onset in Famennian times of glaciations across southern Gondwana. Worldwide evidence for the coeval development of the major Acadian–Eovariscan belt led us to propose a model relating the Late Frasnian–Famennian environmental perturbations to extensive continental uplift through two atmospheric CO₂-depleting mechanisms: (1) the intensification of silicate weathering on the continental areas as attested by a major rise in the ⁸⁷Sr/⁸⁶Sr composition of sea water at the FFB; and (2) the massive burial of organic carbon (Kellwasser events) in partially confined basins due to the collisional-induced reduction of equatorial oceanic communications between the Palaeotethysian and Panthalassic oceans. This process is also suggested to have been controlled by an important primary productivity connected to an increased nutrient availability triggered by the enhanced continental run-off.     

Comparison of laboratory testing protocols to field observations of the weathering of sulfide-bearing mine tailings

A laboratory weathering study using a humidity cell procedure was conducted on two sulfide-bearing tailing samples from a metallurgical site in Ontario (Canada). The test was accompanied by microbiological studies to enumerate the major groups of sulfur-oxidizing bacteria and determine their potential role at different stages during the oxidation process. To evaluate the utility of this method, results were compared with those of previous laboratory and field studies on the same materials. The mineralogy of the laboratory samples differs only by the addition of a small amount of hydronium-bearing natrojarosite [(Na,H₃O)Fe₃(SO₄)₂(OH)₆] to one sample. The progress of sulfide oxidation and the rates of solute release were determined to evaluate the extent of mineral dissolution. These processes were influenced strongly by the capacity of the material to generate acidity, which was enhanced by the presence of hydronium-bearing natrojarosite. Acid-neutralization processes occurring during the laboratory tests were affected by reaction kinetics, consistent with field observations. In particular, the extent of carbonate-mineral dissolution appears to be different in the laboratory than in the field, where more prolonged rock–water interaction allowed more complete chemical equilibration. As a consequence, the capacity of this test procedure to predict weathering reactions in mine tailings is limited by its inability to reproduce the weathering sequence observed in the field. The results of the microbiological study showed that distinct groups of sulfur-oxidizing bacteria operate at different stages of the oxidative process, as was observed in field studies where tailings oxidation occurred under natural conditions, suggesting that microbiological tests performed for laboratory studies are reflective of field conditions.     

Effects of temperature on silicate weathering: Solute fluxes and chemical weathering in a temperate rain forest watershed,Jamieson Creek,British Columbia

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.     

Multiring-forming large bolide impacts and evolution of planetary surfaces

In the past few years, meteoritic and cometary impacts have emerged as a major geological agent in the construction and evolution of planetary surfaces. Formation of complex central ring, peak ring and multiring craters involves excavation and melting of large volumes of crustal material. High-resolution geophysical mapping measuring gravity, magnetics, and topography of the Moon and Mars have recently provided information on the subsurface structure of large basins and aided in identifying buried giant craters. The terrestrial crater record has been significantly erased by tectonic, magmatic, and erosion processes and only a small proportion of impact structures remain. Record of multiring craters is limited to three examples: Vredefort, Sudbury and Chicxulub. Deep geophysical surveys and geochemical and isotopic studies of those craters provide means to evaluate the influence of large impacts on the lithospheric and crustal evolution by providing estimates of excavation depth and volume, amounts of material fragmented, ejected, vaporized and melted, and effects on the crustal stratigraphy and crustal thickness. Analyses on the melt from Vredefort, Sudbury, and Chicxulub indicate andesitic composition derived from lower-crustal material. The melt formed inside the lower transient cavity from lower crustal material that was then redistributed and emplaced in upper-crustal levels, resulting in crustal redistribution. Crystalline basement clasts fragmented and incorporated into the breccias show varying degrees of alteration but no significant thermal effects. Ejecta were deposited locally within the crater region and ballistic material and fine ejecta are globally distributed on the planetary surface. Impacts influence the crust–mantle boundary, with Moho uplift. Material from the mantle was not incorporated into the melt and impact breccias, indicating that the excavation cavities were confined to the lower crust. This is also apparently the case for the giant basins on the Moon, including the 2500 km diameter South Pole-Aitken Basin. Considering the numbers of large multiring basins, possible flux of large impacts, and effects on target surfaces, crustal scale redistribution of material during those large impacts has played a major role in the evolution of planetary surfaces.     

An overview of the role of weathering in the production of quartz silt

Quartz silt is a widespread detrital sediment with large aeolian (loess) and alluvial silt deposits forming important components of many contemporary landscapes. Despite research findings which indicate that a range of opportunities exist for the comminution of quartz into silt particles within a wide variety of geomorphic environments (e.g. glacial grinding, fluvial comminution, aeolian abrasion, frost weathering, salt weathering, insolation weathering and deep weathering), the ‘glacial-aeolian’ hypothesis has traditionally been favoured as the most likely explanation for loess formation and loess is seen as primarily a Quaternary phenomenon. As a consequence there has been a tendency to underestimate sediment inputs into loess systems by geomorphological processes operating within pre-Quaternary environments. In particular, earth scientists may have considerably underestimated the role of weathering in global silt generation, as there are now many references to the existence of a patchy but widespread distribution of pre-Quaternary weathering profiles across the glacial and periglacial landscapes of the Northern Hemisphere (e.g. North America, British Isles, north and central Europe), landscapes within which many of the classical loess deposits are located. These observations suggest that weathering profiles may have covered large tracts of the Northern Hemisphere land surface prior to the Quaternary glaciations. This, in turn, may have important implications for quartz silt generation as: (1) experimental studies indicate that many weathering processes are capable of generating significant quantities of silt-sized debris, and (2) particle characteristics displayed by saprolitic material that has developed on quartz rich crystalline source rocks often include significant quantities of either silt-sized material, or quartz grains that are weakened by weathering derived microfractures. Thus, weathering profiles may represent ‘mines’ of actual and potential quartz silt, available for release into sedimentary systems when these profiles are subsequently reworked by geomorphological processes such as glacial, fluvial and aeolian erosion.     

Stream geochemistry, chemical weathering and CO2 consumption potential of andesitic terrains, Dominica, Lesser Antilles

Recent studies of chemical weathering of andesitic-dacitic material on high-standing islands (HSIs) have shown these terrains have some of the highest observed rates of chemical weathering and associated CO₂ consumption yet reported. However, the paucity of stream gauge data in many of these terrains has limited determination of chemical weathering product fluxes. In July 2006 and March 2008, stream water samples were collected and manual stream gauging was performed in watersheds throughout the volcanic island of Dominica in the Lesser Antilles. Distinct wet and dry season solute concentrations reveal the importance of seasonal variations on the weathering signal. A cluster analysis of the stream geochemical data shows the importance of parent material age on the overall delivery of solutes. Observed Ca:Na, HCO₃:Na and Mg:Na ratios suggest crystallinity of the parent material may also play an important role in determining weathering fluxes. From total dissolved solids concentrations and mean annual discharge calculations we calculate chemical weathering yields of (6-106 t km⁻² a⁻¹), which are similar to those previously determined for basalt terrains. Silicate fluxes (3.1-55.4 t km⁻² a⁻¹) and associated CO₂ consumption (190-1575 × 10³ mol km⁻² a⁻¹) determined from our study are among the highest determined to date. The calculated chemical fluxes from our study confirm the weathering potential of andesitic-dacitic terrains and that additional studies of these terrains are warranted.     

Silicate weathering in anoxic marine sediments

Two sediment cores retrieved at the northern slope of Sakhalin Island, Sea of Okhotsk, were analyzed for biogenic opal, organic carbon, carbonate, sulfur, major element concentrations, mineral contents, and dissolved substances including nutrients, sulfate, methane, major cations, humic substances, and total alkalinity. Down-core trends in mineral abundance suggest that plagioclase feldspars and other reactive silicate phases (olivine, pyroxene, volcanic ash) are transformed into smectite in the methanogenic sediment sections. The element ratios Na/Al, Mg/Al, and Ca/Al in the solid phase decrease with sediment depth indicating a loss of mobile cations with depth and producing a significant down-core increase in the chemical index of alteration. Pore waters separated from the sediment cores are highly enriched in dissolved magnesium, total alkalinity, humic substances, and boron. The high contents of dissolved organic carbon in the deeper methanogenic sediment sections (50-150 mg dm⁻³) may promote the dissolution of silicate phases through complexation of Al³⁺ and other structure-building cations. A non-steady state transport-reaction model was developed and applied to evaluate the down-core trends observed in the solid and dissolved phases. Dissolved Mg and total alkalinity were used to track the in-situ rates of marine silicate weathering since thermodynamic equilibrium calculations showed that these tracers are not affected by ion exchange processes with sediment surfaces. The modeling showed that silicate weathering is limited to the deeper methanogenic sediment section whereas reverse weathering was the dominant process in the overlying surface sediments. Depth-integrated rates of marine silicate weathering in methanogenic sediments derived from the model (81.4-99.2 mmol CO₂ m⁻² year⁻¹) are lower than the marine weathering rates calculated from the solid phase data (198-245 mmol CO₂ m⁻² year⁻¹) suggesting a decrease in marine weathering over time. The production of CO₂ through reverse weathering in surface sediments (4.22-15.0 mmol CO₂ m⁻² year⁻¹) is about one order of magnitude smaller than the weathering-induced CO₂ consumption in the underlying sediments. The evaluation of pore water data from other continental margin sites shows that silicate weathering is a common process in methanogenic sediments. The global rate of CO₂ consumption through marine silicate weathering estimated here as 5-20 Tmol CO₂ year⁻¹ is as high as the global rate of continental silicate weathering.     

Plant and mycorrhizal driven silicate weathering: Quantifying carbon flux and mineral weathering processes at the laboratory mesocosm scale

The rise of vascular land plants in the Paleozoic is hypothesized to have driven lower atmospheric CO₂ levels through enhanced weathering of Ca and Mg bearing silicate minerals and rocks. However, this view overlooks the co-evolution of roots and mycorrhizal fungi, with many of the weathering processes ascribed to plants potentially being driven by the combined activities of roots and fungi. Here mesocosm scale controlled laboratory experiments quantifying the effects of plant and fungal evolution on silicate rock weathering under ambient and elevated CO₂ concentrations are described. A snapshot is presented of C allocation through roots and mycorrhizal fungi and biological activity associated with geochemical changes in weathered mineral substrates via transfer of elements from solid phases into solution.     

Chemical alteration in the micro weathering environment within a spheroidally-weathered anorthosite boulder

A chemical and mineralogical study of the innermost rindlets of a spheroidally weathered boulder from the Wichita Mountains, Oklahoma details incipient alteration of minerals along solution channels. Alteration products in plagioclase areas are highly aluminous, whereas ferruginous residuum is commonly found in olivine alteration zones. Alteration of plagioclase along solution channels results in sharp weathering contacts as contrasted with wider zones of “limonite” bordering solution channels in olivine. In certain instances, cores of fresh olivine are surrounded by limonite indicating that diffusion may play a role in this type of alteration.Mobility of sesquioxides is evidenced by aluminum-rich debris adjacent to mafic materials in solution channels and iron-bearing material in channels cutting through plagioclase. Not resolved is whether the movement of sesquioxides in solution channels is by transport of colloidal particulates or by diffusion of dissolved species.Calcic plagioclase alters to calcite along the innermost solution channel. It is postulated that solution, exterior to the boulder and undersaturated with respect to calcite, enters the rind system via solution channels. Cut off from the CO₂ reservoir of the atmosphere by the narrow confines of this solution channel, the solution reacts with the bytownite to precipitate calcite.Apart from the occurrence of calcite, no crystalline weathering products were found in the innermost rindlet samples. A poorly crystallized illite was identified in the outermost rindlet. These findings suggest that initial alteration products on weathering rinds are amorphous and that, with time, these products attain a degree of identifiable crystallinity.     

Al_2O_3/Ti:风化与蚀变过程中的原岩示踪

Al_2O_3和Ti在风化和热液蚀变等地球化学过程中通常被认为是不活动元素,两者的比值Al_2O_3/Ti常被用来指示地球化学作用过程。通过对中国157件火成岩样品元素含量平均值的统计发现,火成岩样品中Al_2O_3/Ti与SiO_2含量值之间存在着较好的幂函数关系:ln(Al_2O_3/Ti)=0.073×SiO_2-0.89,式中Al_2O_3和SiO_2和Ti含量单位均为%。本文基于得到的经验方程和TAS图解构建了一个新的判别岩石类型的图解——Al_2O_3-Ti图解。该图解可以区分酸性岩、中酸性岩、中性岩、中基性岩-基性岩四类岩性。通过对三个火成岩风化剖面的研究发现,花岗岩风化剖面从新鲜基岩到风化形成的土壤在Al_2O_3-Ti图解中均落在酸性岩区,花岗闪长岩风化剖面从新鲜基岩到风化形成的土壤样品均落在中酸性岩区,玄武质安山岩风化剖面从新鲜基岩到风化形成的土壤样品均落在中基性岩-基性岩区。不同风化程度的风化产物与其母岩在Al_2O_3-Ti图解中所在的区域一致,即Al_2O_3-Ti图解可以用来追溯火成岩风化产物的母岩岩性。通过对胶东焦家金矿和豫西牛头沟金矿两个矿区岩石的研究发现,黑云母花岗岩从新鲜岩石到其蚀变岩及其形成矿石的样品在Al_2O_3-Ti图解中均落在酸性岩区。玄武质安山岩从新鲜岩石到其蚀变岩及其形成矿石的样品在Al_2O_3-Ti图解中均落在中基性岩-基性岩区。即不同蚀变程度的蚀变产物与其原岩在Al_2O_3-Ti图解中所在的区域一致,这表明新构建的Al_2O_3-Ti图解可以用来示踪蚀变岩的原岩性质。