Chemical Weathering Of Silicate Minerals Research Articles

Enhanced olivine dissolution in seawater through continuous grain collisions

Carbon dioxide removal (CDR) technologies at a gigaton scale need to be developed and implemented within the next decades to keep global warming below 1.5 °C. Coastal enhanced silicate weathering is one of the proposed CDR techniques that aims to accelerate the natural process of CO2-sequestration during marine chemical weathering of silicate minerals. To this end, finely ground rock containing olivine (MgxFe2−xSiO4) could be dispersed in dynamic coastal environments, where local biotic and abiotic factors potentially enhance the weathering process. However, accurate predictions of the olivine dissolution rate and the associated CO2 sequestration under in situ conditions are currently lacking and ecosystem impacts remain to be assessed. Previously, it has been hypothesized that in situ grain collisions, induced by bed load transport due to currents and waves, could accelerate the in situ chemical weathering of olivine particles. To examine this, we investigated the effects of continuous grain tumbling on olivine dissolution in natural seawater. A 70-day experiment was conducted in which forsterite olivine sand was continuously tumbled in filtered seawater at different rotation speeds, and dissolution rates were measured on a weekly basis. Results showed that continuously tumbled olivine dissolved 8 to 19 times faster compared to stagnant (no rotation) conditions. Olivine dissolution was complete and stoichiometric (except for Ni release), air-seawater CO2 exchange was not significantly rate limiting, and minimal particle fragmentation and secondary mineral formation were observed. Hence, we infer that olivine weathering was mainly enhanced via advective pore water flushing, which limits saturation effects at the grain scale. Overall, this study provides evidence that ambient physical stresses in coastal environments could enhance marine silicate weathering, which has implications for both the natural silicon cycle as well as the use of enhanced coastal weathering of silicates as a CDR technique.

Elevated physical weathering exceeds chemical weathering of clays during the Paleocene-Eocene Thermal Maximum in the continental Bighorn Basin (Wyoming, USA)

The Paleocene-Eocene Thermal Maximum (PETM) global warming event at ∼56 million years before present changed catchment weathering and erosion. Increased chemical weathering of silicate minerals is thought to be an important process removing CO2 from the atmosphere. However, changes in clay mineralogy can often be explained by enhanced erosion of catchment laterites during the event. Here, we investigate chemical and physical weathering and erosive flux changes through the PETM interval in the Bighorn Basin, Wyoming, a Laramide foreland basin, in a proximal continental-interior alluvial setting. These show an increase of detrital smectite with a lag time of 20-kyr after the main onset the PETM. The smectite increase continued for at least 50-kyr after the event. In-situ, post-depositional pedogenic clay mineral formation is similar between pre-PETM and PETM soil profiles, despite large macroscopic differences between soils that formed before and during the event. Drier, hotter summers during the PETM probably caused decreased vegetation cover that, in concert with more frequent and heavier rainstorms, intensified the erosion of smectite-rich Cretaceous bentonites on the margins of the catchment, which exceeded changes in chemical weathering within the catchment. The lagged response in reaching full PETM clay mineral values can be explained by the time required for upstream sediment to reach the catchment basin floodplain. The prolonged nature of smectite enhancement after the PETM event may again relate to signal propagation times that are now even longer due to lower fluvial recycling rates. Our results indicate that chemical weathering changes were probably superceded by enhanced physical weathering and clay-mineral transport from basin margins at this continental-interior study site.

Behavior of Li, S and Sr isotopes in the subterranean estuary and seafloor pockmarks of the Hanko submarine groundwater discharge site in Finland, northern Baltic Sea

The impact of submarine groundwater discharge (SGD) on coastal sea biogeochemistry and water quality has been demonstrated in many recent studies. However, the isotopic behavior of terrestrially-derived solutes in the groundwater-seawater mixing zone of coastal aquifers (the subterranean estuary, STE) has been less studied, although solutes such as Li, S and Sr are commonly used as tracers of weathering and biogeochemical processes taking place in aquifers and in coastal sea sediments. This study investigated the behavior of 87Sr/86Sr, δ7Li and δ34S in the STE and three seafloor pockmarks with different degrees of groundwater influence, as constrained based on δ2H and δ18O, at the Hanko SGD site in Finland, in the northern Baltic Sea. These data were supplemented by groundwater and seawater measurements. 87Sr/86Sr showed non-conservative behavior with values elevated up to 0.0167 units above that expected for the conservative mixing in the STE and in the most groundwater-dominated pockmark (up to 100% groundwater), but the deviation was masked by much stronger seawater contributions in the other pockmarks. δ7Li values were shifted down to −1.75‰ below that expected for conservative mixing in the STE and in groundwater-influenced pockmark porewaters, whereas δ7Li was elevated up to 1.53‰ in the porewater of organic-rich mud in a pockmark where groundwater influence had ceased. δ34S deviated between −16.78‰ and 10.51‰ from the conservative mixing in the STE and porewaters of groundwater-influenced pockmarks, while δ34S was elevated up to 16.85‰ in the porewater of the pockmark with no groundwater influence. In the STE, the isotopic fractionation of Sr and Li was explained by chemical weathering of silicate minerals and clay minerals, respectively, whereas δ34S was fractionated by complex interactions of microbial sulfate reduction and sulfide reoxidation. In the pockmark porewater with no groundwater influence, δ7Li and δ34S isotopes were enriched in the heavier isotopes as a consequence of early-diagenetic mineral formation in the organic-rich muds. The measured 87Sr/86Sr and δ7Li were higher than the previously estimated isotopic compositions of their groundwater-derived fluxes to the oceans, and partly higher than the global riverine values. The heterogeneity in the seafloor biogeochemical environment, caused by the focusing of SGD in pockmarks, resulted in strongly variable δ34S of groundwater-derived S flux to the coastal ocean at a spatial scale of a few hundreds of meters.

The supercontinent cycle and Earth's long-term climate.

Earth's long-term climate has been profoundly influenced by the episodic assembly and breakup of supercontinents at intervals of ca. 500 m.y. This reflects the cycle's impact on global sea level and atmospheric CO2 (and other greenhouse gases), the levels of which have fluctuated in response to variations in input from volcanism and removal (as carbonate) by the chemical weathering of silicate minerals. Supercontinent amalgamation tends to coincide with climatic cooling due to drawdown of atmospheric CO2 through enhanced weathering of the orogens of supercontinent assembly and a thermally uplifted supercontinent. Conversely, breakup tends to coincide with increased atmospheric CO2 and global warming as the dispersing continental fragments cool and subside, and weathering decreases as sea level rises. Supercontinents may also influence global climate through their causal connection to mantle plumes and large igneous provinces (LIPs) linked to their breakup. LIPs may amplify the warming trend of breakup by releasing greenhouse gases or may cause cooling and glaciation through sulfate aerosol release and drawdown of CO2 through the chemical weathering of LIP basalts. Hence, Earth's long-term climatic trends likely reflect the cycle's influence on sea level, as evidenced by Pangea, whereas its influence on LIP volcanism may have orchestrated between Earth's various climatic states.

Recharge and Geochemical Evolution of Groundwater in Fractured Basement Aquifers (NW India): Insights from Environmental Isotopes (δ18O, δ2H, and 3H) and Hydrogeochemical Studies

Considering water as a limiting factor for socio-economic development, especially in arid/semi-arid regions, both scientific communities and policymakers are interested in groundwater recharge-related data. India is fast moving toward a crisis of groundwater due to intense abstraction and contamination. There is a lack of understanding regarding the occurrence, movement, and behaviors of groundwater in a fractured basement terrane. Therefore, integrated environmental isotopes (δ18O, δ2H, and 3H) and hydrogeochemical studies have been used to understand the recharge processes and geochemical evolution of groundwater in the fractured basement terranes of Gujarat, NW India. Our results show that the relative abundance of major cations and anions in the study basin are Ca2+ > Na+ > Mg2+ > K+ and HCO3− > Cl− > SO42− > NO3−, respectively. This suggests that the chemical weathering of silicate minerals influences the groundwater chemistry in the aquifer system. A change in hydrochemical facies from Ca-HCO3 to Na-Mg-Ca-Cl. HCO3 has been identified from the recharge to discharge areas. Along the groundwater flow direction, the presence of chemical constituents with different concentrations demonstrates that the various geochemical mechanisms are responsible for this geochemical evolution. Furthermore, the chemical composition of groundwater also reflects that the groundwater has interacted with distinct rock types (granites/granulites). The stable isotopes (δ18O and δ2H) of groundwater reveal that the local precipitation is the main source of recharge. However, the groundwater recharge is affected by the evaporation process due to different geological conditions irrespective of topographical differences in the study area. The tritium (3H) content of groundwater suggests that the aquifer is mainly recharged by modern rainfall events. Thus, in semi-arid regions, the geology, weathering, and geologic structures have a significant role in bringing chemical changes in groundwater and smoothening the recharge process. The findings of this study will prove vital for the decision-makers or policymakers to take appropriate measures to design water budgets as well as water management plans more sustainably.

From on high: Geochemistry of alpine springs, Niwot Ridge, Colorado Front Range, USA

AbstractSnowmelt‐fed springs and small (0.5 km2) upland catchments in alpine areas of the western United States contribute significantly to the quantity and inorganic chemistry of water delivered to downstream basins but have not been studied extensively. Mineral weathering, transit time, and hydrologic mixing control the solute chemistry of waters that drain the upland zone of Niwot Ridge, Colorado Front Range, and adjacent areas in the granitic core of the Southern Rocky Mountains. Water in 37 springs sampled in this study flows in generally short steep paths (~0.3 km) through shallow regolith with mean transit times (MTT) of weeks to months, producing solutions dominated by Si, Ca2+, Na+, and HCO3−, locally SO42−. Rock type is a significant control on spring, surface, and shallow groundwater chemistry, and plagioclase (oligoclase) is the major source of dissolved Na+ and Si. Concentrations of Ca2+ exceed stoichiometric predictions of oligoclase weathering by ~3.5×; excess Ca2+ likely represents weathering of aeolian material, vein calcite, or trace minerals. Concentrations of base cations and Si increase slowly with estimated MTT of 0.2 years for Niwot Ridge spring waters, and several years for shallow groundwater sampled by wells. Chemical weathering of silicate minerals is slow with estimated rates of ~2.0 and 0.2 pmol·m−2·s−1 for oligoclase and microcline, respectively; the most mineralized spring waters are saturated only with respect to kaolinite and montmorillonite. More than 50% of the dissolved base cations + Si measured in Boulder Creek at Orodell (~25 km downstream) accumulate before water emerges from alpine springs on Niwot Ridge. Warming global temperatures are shifting more high‐elevation precipitation to rain, potentially changing run‐off patterns, transit time, and solute loads. Acquisition of solutes by alpine waters thus has implications far beyond small upland catchments.

Calcium isotope fractionation in a silicate dominated Cenozoic aquifer system

To understand the characteristics of Ca isotope composition and fractionation in silicate-dominated Quaternary aquifer system, hydrochemical and isotope studies (87Sr/86Sr, 13CDIC and 44/40Ca) were conducted on groundwater, sediment and rock samples from the Datong basin, China. Along the groundwater flow path from the basin margin to the center, groundwater hydrochemical type evolves from Ca-HCO3 to Na-HCO3/Na-Cl type, which results from aluminosilicate hydrolysis, vertical mixing, cation exchange between CaX2 and NaX, and calcite/dolomite precipitation. These processes cause the decrease in groundwater Ca concentration and the associated modest fractionation of groundwater Ca isotopes along the flowpath. The groundwater δ44/40Ca value varies from −0.11 to 0.49‰. The elevated δ44/40Ca ratios in shallow groundwater are attributed to vertical mixing involving addition of irrigation water, which had the average δ44/40Ca ratio of 0.595‰. Chemical weathering of silicate minerals and carbonate generates depleted δ44/40Ca signatures in groundwater from Heng Mountain (east area) and Huanghua Uplift (west area), respectively. Along the groundwater flow path from Heng Mountain to central area of east area, cation exchange between CaX2 and NaX on clay mineral results in the enrichment of heavier Ca isotope in groundwater. All groundwater samples are oversaturated with respect to calcite and dolomite. The groundwater environment rich in organic matter promotes the precipitation of carbonate minerals via the biodegradation of organic carbon, thereby further promoting the elevation of groundwater δ44/40Ca ratios.

Predicting soil formation on the basis of transport-limited chemical weathering

Soil production is closely related to chemical weathering. It has been shown that, under the assumption that chemical weathering is limited by solute transport, the process of soil production is predictable. However, solute transport in soil cannot be described by Gaussian transport. In this paper, we propose an approach based on percolation theory describing non-Gaussian transport of solute to predict soil formation (the net production of soil) by considering both soil production from chemical weathering and removal of soil from erosion. Our prediction shows agreement with observed soil depths in the field. Theoretical soil formation rates are also compared with published rates predicted using soil age-profile thickness (SAST) method. Our formulation can be incorporated directly into landscape evolution models on a point-to-point basis as long as such models account for surface water routing associated with overland flow. Further, our treatment can be scaled-up to address complications associated with continental-scale applications, including those from climate change, such as changes in vegetation, or surface flow organization. The ability to predict soil formation rates has implications for understanding Earth's climate system on account of the relationship to chemical weathering of silicate minerals with the associated drawdown of atmospheric carbon, but it is also important in geomorphology for understanding landscape evolution, including for example, the shapes of hillslopes, and the net transport of sediments to sedimentary basins.

Lithium isotopes in speleothems: Temperature-controlled variation in silicate weathering during glacial cycles

Terrestrial chemical weathering of silicate minerals is a fundamental component of the global cycle of carbon and other elements. Past changes in temperature, rainfall, ice cover, sea-level and physical erosion are thought to affect weathering but the relative impact of these controls through time remains poorly constrained. This problem could be addressed if the nature of past weathering could be constrained at individual sites. In this study, we investigate the use of speleothems as local recorders of the silicate weathering proxy, Li isotopes. We analysed δ7Li and [Li] in speleothems that formed during the past 200 ka in two well-studied Israeli caves (Soreq and Tzavoa), as well as in the overlying soils and rocks. Leaching and mass balance of these soils and rocks show that Li is dominantly sourced from weathering of the overlying aeolian silicate soils. Speleothem δ7Li values are ubiquitously higher during glacials (∼23‰) than during interglacials (∼10‰), implying more congruent silicate weathering during interglacials (where “congruent” means a high ratio of primary mineral dissolution to secondary mineral formation). These records provide information on the processes controlling weathering in Israel. Consideration of possible processes causing this change of weathering congruency indicates a primary role for temperature, with higher temperatures causing more congruent weathering (lower δ7Lispeleo). The strong relationship observed between speleothem δ7Li and climate at these locations suggests that Li isotopes may be a powerful tool with which to understand the local controls on weathering at other sites, and could be used to assess the distribution of weathering changes accompanying climate change, such as that of Pleistocene glacial cycles.

The dissolution of olivine added to soil: Implications for enhanced weathering

Chemical weathering of silicate minerals consumes atmospheric CO2 and is a fundamental component of geochemical cycles and of the climate system on long timescales. Artificial acceleration of such weathering (“enhanced weathering”) has recently been proposed as a method of mitigating anthropogenic climate change, by adding fine-grained silicate materials to continental surfaces. The efficacy of such intervention in the carbon cycle strongly depends on the mineral dissolution rates that occur, but these rates remain uncertain. Dissolution rates determined from catchment scale investigations are generally several orders of magnitude slower than those predicted from kinetic information derived from laboratory studies. Here we present results from laboratory flow-through dissolution experiments which seek to bridge this observational discrepancy by using columns of soil returned to the laboratory from a field site. We constrain the dissolution rate of olivine added to the top of one of these columns, while maintaining much of the complexity inherent in the soil environment. Continual addition of water to the top of the soil columns, and analysis of elemental composition of waters exiting at the base was conducted for a period of five months, and the solid and leachable composition of the soils was also assessed before and after the experiments. Chemical results indicate clear release of Mg2+ from the dissolution of olivine and, by comparison with a control case, allow the rate of olivine dissolution to be estimated between 10−16.4 and 10−15.5 moles(Mg)cm−2s−1. Measurements also allow secondary mineral formation in the soil to be assessed, and suggest that no significant secondary uptake of Mg2+ has occurred. The olivine dissolution rates are intermediate between those of pure laboratory and field studies and provide a useful constraint on weathering processes in natural environments, such as during soil profile deepening or the addition of mineral dust or volcanic ash to soils surfaces. The dissolution rates also provide critical information for the assessment of enhanced weathering including the expected surface-area and energy requirements.

Tracing silicon cycling in the Okavango Delta, a sub-tropical flood-pulse wetland using silicon isotopes

Chemical weathering of silicate minerals releases elements into solution whereas the neoformation of secondary minerals works in the opposite direction, potentially confounding estimates of silicate weathering rates. Silicon isotopes (δ30Si) may be a useful tool to investigate these processes. Here, we present 82 δ30Si measurements from surface waters, pore waters, biogenic silica (BSi), clays, sand and vegetation from the Okavango Delta, Botswana, a freshwater sub-tropical, flood-pulse wetland. Hydrologically, the Okavango is dominated by evapotranspiration water losses to the atmosphere. It receives an annual pulse of water that inundates seasonal floodplains, while river baseflow is sufficient to maintain a permanent floodplain. δ30Si in dissolved silica (DSi) in surface waters along a 300km transect at near-peak flood show a limited range (0.36–1.19‰), implying the Delta is well buffered by a balance of processes adding and removing DSi from the surface water. A key control on DSi concentrations is the uptake, production of BSi and recycling of Si by aquatic vegetation, although the net isotopic effect is necessarily small since all BSi re-dissolves on short timescales. In the sediments, BSi δ30Si (n=30) ranges from −1.49‰ to +0.31‰ and during dissolution, residual BSi tends towards higher δ30Si. The data permit a field-based estimate of the fractionation associated with BSi dissolution, ε30BSi-DSi=−0.26‰, though it is unclear if this is an artefact of the process of dissolution. Clay δ30Si ranges from −0.97‰ to +0.10‰, (n=15, mean=−0.31‰) and include the highest values yet published, which we speculate may be due to an equilibrium isotope effect during diagenetic transformation of BSi. Two key trends in surface water DSi δ30Si merit further examination: declining δ30Si in an area roughly corresponding to the permanent floodplains despite net DSi removal, and increasing δ30Si in the area corresponding to the seasonal floodplains. We infer that evaporative enrichment of surface waters creates two contrasting regimes. Chemical weathering of low δ30Si phases releases low δ30Si DSi in the relatively dilute waters of the permanent floodplains, whereas silicon removal via clay formation or vegetation uptake is the dominant process in the more enriched, seasonal floodplains.

Is orogenesis a net sink or source of atmospheric CO2?

In global carbon cycle models, orogenesis is often viewed as a sink for atmospheric CO2, acting on tectonic timescales. However, recent attempts to quantify fluxes for CO2 produced by metamorphic reactions and released to the atmosphere suggest that these are an order‐of‐magnitude greater than CO2 uptake by chemical weathering of silicate minerals, and that metamorphic CO2 is released on millennial timescales. These hypotheses have gained support from both measurements of CO2 emissions from present‐day orogenic hot springs and chromatographic modelling of carbonation reactions in metamorphic rocks from ancient orogens. In this article I review research that attempts to quantify metamorphic CO2 release fluxes, focussing specifically on studies conducted in the SW Scottish Highlands.

Mechanism of leached layer formation during chemical weathering of silicate minerals

The dissolution of most common multicomponent silicate minerals and glasses is typically incongruent, as shown by the nonstoichiometric release of the solid phase components. This results in the formation of so-called surface leached layers. Due to the important effects these leached layers may have on mineral dissolution rates and secondary mineral formation, they have attracted a great deal of research. However, the mechanism of leached layer formation is a matter of vigorous debate. Here we report on an in situ atomic force microscopy (AFM) study of the dissolution of wollastonite, CaSiO 3 , as an example of leached layer formation during dissolution. Our in situ AFM results provide, for the first time, clear direct experimental evidence that leached layers are formed in a tight interface-coupled two-step process: stoichiometric dissolution of the pristine mineral surfaces and subsequent precipitation of a secondary phase (most likely amorphous silica) from a supersaturated boundary layer of fluid in contact with the mineral surface. This occurs despite the fact that the bulk solution is undersaturated with respect to the secondary phase. Our results differ significantly from the concept of preferential leaching of cations, as postulated by most currently accepted incongruent dissolution models. This interface-coupled dissolution-precipitation model has important implications in understanding and evaluating dissolution kinetics of major rock-forming minerals.

Major ion composition and carbonate equilibrium in the sediment pore water of the Razdol’naya River estuary of Amur Bay, the Sea of Japan

The complex study of the river water and pore solutions from the bottom sediments in the lower reaches of the Razdol’naya River was conducted in February 2010. The major ion composition of the waters indicates the submarine origin of the near-bottom and pore waters in the lower reaches of the Razdol’naya River in the winter. The river estuary extends upstream for more than 20 km. It was established that the studied sediments are reduced oozes containing pyrite, hydrotroilite, and iron monosulfide, which is direct evidence for sulfate-reduction in the sediments. The diagenesis of organic matter is the main reason for the considerable decrease in the amount of sulfates and the increase in the alkalinity of the sediment pore water. The sedimentary pore water sampled from the deep river pits is characterized by excess alkalinity that cannot be explained by sulfate-reduction and methane genesis. It was suggested that the chemical weathering of silicate minerals and the bacterial mineralization of salts of organic acids could result in the excess alkalinity of the sediment pore water.

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 CO 2, 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.

Elevated weathering rates in the Rocky Mountains during the Early Eocene Climatic Optimum

Silicate weathering reactions remove carbon dioxide from the atmosphere and store it in carbonate minerals. During the high atmospheric carbon dioxide conditions of the Early Eocene Climatic Optimum, rates of chemical weathering, physical erosion and denudation in the western USA were equivalent to the highest recorded rates in the non-glacial Quaternary. During the chemical weathering of silicate minerals, atmospheric carbon dioxide is incorporated into carbonate minerals and buried. As the rate of silicate weathering is thought to increase in response to increasing atmospheric CO2 concentrations, this represents an important negative feedback mechanism1. Quaternary records of weathering reflect a narrow range of pCO2 (180–300 p.p.m.v.)2; therefore, the extent of this feedback has been difficult to predict for increasing concentrations of atmospheric CO2. However, high CO2 levels of up to 1,125 p.p.m.v. have been suggested for the Early Eocene Climatic Optimum (52 to 50 million years ago)3,4,5. Here, we combine 40Ar/39Ar ages6 and the measured volumes of river-derived sediments and sodium-bearing evaporites to determine rates of physical erosion and chemical weathering in the Green River Basin, western United State of America, during the Early Eocene Climatic Optimum7. We find physical erosion rates of 420±79 t km2 yr−1 and chemical weathering rates of 62.5±21.9 t km2 yr−1. The calculated denudation rates of 175±30 m Myr−1 rival the highest documented non-glacial Quaternary rates for crystalline bedrock8. We suggest that elevated atmospheric CO2 levels during the Early Eocene epoch led to enhanced silicate dissolution rates9, and thus to increased production of loose rock material and higher rates of physical weathering and denudation.

Carbonate verse silicate Sr isotope in lake sediments and its response to Little Ice Age

The87Sr/86Sr ratios of silicate (acid-insoluble, AI) and carbonate (acid-soluble, AS) of the lake sediments from the Daihai Lake, Inner Mongolia, since the last 500 years are measured respectively, indicating that chemical weathering of silicate minerals was in an early stage since the Little Ice Age within the Daihai watershed by combination with mineral constitute, Rb/Sr ratio and CaCO3 content in the sediments. During the Little Ice Age maximum, an evident peak in the87Sr/86Sr ratios of both silicate and carbonate in sediments suggests that a cold climate condition is unfavorable to dissolving radiogenic strontium from silicate minerals. Meanwhile, the variation of87Sr/86Sr ratios of silicate and carbonate also reflects a projected warming climate favorable to intensifying chemical weathering after the Little Ice Age. Consequently, the87Sr/86Sr ratio of both silicate and carbonate in inland lake sediments can be used as an effective proxy of the past climate in single watershed.

A study of environmental analysis of urban river sediments using activation analysis

Sediments of the Kitajukkengawa River (Sumida-ku, Tokyo, Japan) were analyzed by activation analyses. Concentrations of 36 elements for each sample were determined by instrumental neutron activation analysis (INAA) and neutron induced prompt gamma-ray analysis (PGA). Based on the correlation matrix between the elements in vertical distribution, principal component analysis (PCA) was performed. The degree of chemical weathering of silicate minerals was highest in the middle layer of the Kitajukkengawa River sediment and that adsorbed amount of trace metals such as Cd and Cr was increased along with chemical weathering.

Tracing spatial and temporal variations in the sources of calcium in pedogenic carbonates in a semiarid environment

In arid environments, significant amounts of calcium (Ca) are stored in pedogenic carbonates that develop in soils. There are two sources for Ca in pedogenic carbonates in soils: local parent material and dust deposited on the surface. In this study, the strontium (Sr) isotopes ( 87Sr/ 86Sr ratios) were used as a tracer for Ca from these sources. We studied spatial and temporal variations in the sources of Ca in pedogenic carbonates in soils developed in six Quaternary basalt flows and a cinder deposit in the Zuni–Bandera volcanic field near Grants, NM. Young basalt is an excellent rock type on which to study soil development because it provides a chemically and isotopically uniform substrate. Age dating of the flows provides control for the beginning of soil development. Other rock types (with varying 87Sr/ 86Sr ratios) cropping out around the basalt provide an opportunity to evaluate spatial variations in sources of Ca and Sr. The 87Sr/ 86Sr ratio of pedogenic carbonates (average 0.7078) is similar to the average ratio of marine limestone cropping out in the region, and is distinctly different from that of basalt bedrock (average 0.7053), indicating that chemical alteration of dust is the principle source of Ca. There is a strong correlation between the 87Sr/ 86Sr ratio of pedogenic carbonate and the labile fraction of dust and A soil horizon samples. There is little correlation between the 87Sr/ 86Sr ratio of pedogenic carbonate and that of the residual (silicate) fraction of dust or A horizon samples. This indicates that the major source of Ca cycling through these soils is chemical weathering of carbonate minerals in dust and that only a minor component is from chemical weathering of silicate minerals, either in dust or the underlying basalt. Mixing calculations using Sr isotopes as a tracer for Ca support the qualitative observations. Some variability in the 87Sr/ 86Sr ratio of pedogenic carbonates was found on a local scale (several hundred meters to several kilometers), and can be attributed to changes in dust composition due to contributions from local bedrock. There was no correlation found between the age of a basalt flow and the 87Sr/ 86Sr ratio of the pedogenic carbonate developed on them, indicating that the composition of dust has not changed significantly over the last 0.7 Ma.

化学的風化作用の河川水水質，特に溶存シリカ濃度に与える影響

Chemical weathering of silicate minerals in rocks controls the dissolved silica concentration of riverwater. This means that the dissolution rate of silicate minerals is an important factor for dissolved silica concentration. In addition to the dissolution rate, runoff (Δf) is also an important factor controlling riverwater chemistry. Therefore, the relationshipof the dissolved silica concentration, runoff, and dissolution rate of silicate mineral (feldspar) were theoretically derived on the basis of a dissolution kinetics-fluid flow coupling model. This theoretical consideration indicates that the parameter, φk (A/M), in which φ : porosity, h : thickness of reservoir of groundwater, k : dissolution rate constant, together with Δf, affects the dissolved silica concentration. If Δf is low compared to φ hk (AIM), the concentration (C) is equal to the equilibrium concentration. If Δf is high, C negatively correlates with Lf. This theoretical curve showing the relationship between the dissolved silica concentration and runoff is consistent with the dissolved silica concentration and runoff data of a major global riverwater.