Weathering Rates Research Articles

The dissolution of olivine added to soil at 32°C: the fate of weathering products and its implications for enhanced weathering at different temperatures

The amendment of agricultural soils by crushed silicate minerals has been proposed to enhance weathering rates and facilitate carbon dioxide (CO2) removal from the atmosphere. Laboratory dissolution experiments typically provide weathering rates that are significantly higher than those observed under natural conditions, while field studies are limited in the nature of data they can collect. This study uses an experimental setup that aims to emulate natural field conditions in a controlled setting using soil cores retrieved from UK cropland amended with crushed olivine at 32°C. Results are compared to enhanced weathering experiments run at 4°C and 19°C under otherwise identical conditions. The data reveal temperature-dependent variations in the behaviour of different elements, most importantly Mg and Si, with silicon being retained at moderate temperatures and magnesium being retained at higher temperatures. These patterns are most likely due to different retention mechanisms, notably Si reprecipitation (e.g. as cation-depleted Si-enriched mineral surface coatings) and cation exchange (affecting Mg, but to a lesser degree Si), such that the influence of cation exchange should be accounted for when interpreting enhanced weathering field data. We therefore recommend that estimates of carbon sequestration should not be based on the behaviour of individual elements. A temperature effect on the weathering rate of olivine added to soil columns is observed with the weathering rate being higher at 32°C than at 19°C and 4°C, and significantly lower than laboratory experiment-derived weathering rates. This further emphasises the need for enhanced weathering field trials, as simple laboratory-derived rates cannot be used to assess the feasibility of enhanced weathering measures. The carbon dioxide capture potential at 32°C is conservatively estimated at ~115 t CO2 km-2 yr-1 assuming an olivine amendment rate of 12.7 kg m-2. Our data suggests that soil accumulation of heavy metals like Cu and Cr at high temperatures (hence high weathering rates) is non-dangerous, however, Ni concentrations in the effluent solution are close to EU guidelines while Cr and Cu are considerably lower than guidelines. All of these conclusions have implications for the application of enhanced weathering for carbon dioxide removal from the atmosphere.

Chemical weathering processes in the Chinese Loess Plateau

Covered by erodible loess and affected by significant seasonal climate variations, chemical weathering in the Chinese Loess Plateau (abbreviated as CLP) has important effects on the hydrochemistry of the Yellow River and the global carbon cycle. However, chemical weathering processes in the CLP are still unclear. Based on 296 river water samples in the CLP in the different seasons, hydrochemistry, weathering processes, and their controlling factors were revealed. River waters in the CLP exhibited slightly alkalinity (pH = 8.4 ± 0.5) with much high total dissolved solids (TDS) values (691 ± 813 mg/L). The water types of river water in the CLP were primarily SO42− − Cl− − Na+, HCO3− − Ca2+ − Mg2+, and SO42− − Cl− − Ca2+ − Mg2+. According to the forward model, evaporite dissolution has the largest contribution (55.1% ± 0.2%) to riverine solutes in the CLP, then followed by carbonate weathering (35.6% ± 0.2%) and silicate weathering (6.5% ± 0.1%). For spatio-temporal variations, the contribution of evaporite dissolution in the CLP decreased from northwest to southeast with higher proportion in the dry season, carbonate weathering increased from northwest to southeast with a higher proportion in the wet season, and silicate weathering showed minor spatio-temporal variations. Ca2+ and Mg2+ were affected by carbonate precipitation and/or incongruent calcite dissolution, and about 50% of samples exhibited cation exchange reactions. The physical erosion rate in the CLP, which was 372 ± 293 t·km−2·yr−1, varied greatly and was greater than those of other worldwide rivers. Chemical weathering rates in the CLP showed an increasing trend southward. During the wet season, high runoff led to the release of evaporite and carbonate from loess, while the interfacial reaction kinetic limited the increase of the silicate weathering rates. The CO2 consumption budget by carbonate weathering (6.1 × 1010 mol/yr) and silicate weathering (1.6 × 1010 mol/yr) in the CLP accounted for 0.29% and 0.08% of the global carbon cycle, respectively. Meanwhile, the weathering proportion by sulfuric acids was relatively high with a CO2 release flux of 6.5 × 109 mol/yr. By compiling the data, we propose that the interfacial reaction kinetic and runoff control CO2 consumption rate by silicate and carbonate weathering, respectively. These results contribute to the understanding of modern weathering processes of loess in the CLP, thus helping to deduce the environmental and climatic evolution of the basin.

Middle Eocene Climatic Optimum (MECO) and its imprint in the continental Escanilla Formation, Spain

Abstract. The Middle Eocene Climatic Optimum (MECO) is a global warming event mainly recognized in the marine domain and described less in the terrestrial environment. Here we present a comprehensive geochemical record of the MECO from the Escanilla Formation, a fluvial sedimentary succession in the southern Pyrenees, Spain, based on a suite of sampled paleosols, fluvial stromatolites, and pedogenic nodules. Our multiproxy approach involves using carbon and oxygen stable isotope compositions to identify the regional preservation of the MECO, calculate chemical weathering intensity and mean annual precipitation, perform clumped isotopes on carbonates, and identify clay mineralogy assemblages of paleosols. Results indicate that the Middle Eocene interval in the southern Pyrenees was characterized by low weathering rates under warm and arid climatic conditions. This is further supported by the presence of smectite, palygorskite, illite, and chlorite, which suggest seasonal rainfall but under generally dry conditions resulting in weak chemical weathering. Importantly, a negative organic carbon isotopic excursion indicates the regional, terrestrial impact of the MECO, highlighting that fluvial sedimentary successions even in active foreland basins can represent particularly interesting terrestrial archives of past changes in global climate.

Organic carbon source controlled microbial olivine dissolution in small-scale flow-through bioreactors, for CO2 removal

The development of carbon dioxide removal methods, coupled with decreased CO2 emissions, is fundamental to achieving the targets outlined in the Paris Agreement limiting global warming to 1.5 °C. Here we are investigating the importance of the organic carbon feedstock to support silicate mineral weathering in small-scale flow through bioreactors and subsequent CO2 sequestration. Here, we combine two bacteria and two fungi, widely reported for their weathering potential, in simple flow through bioreactors (columns) consisting of forsterite and widely available, cheap organic carbon sources (wheat straw, bio-waste digestate of pig manure and biowaste, and manure compost), over six weeks. Compared to their corresponding abiotic controls, the inoculated straw and digestate columns release more total alkalinity (~2 times more) and produce greater dissolved and solid inorganic carbon (29% for straw and 13% for digestate), suggesting an increase in CO2 sequestration because of bio-enhanced silicate weathering. Microbial biomass is higher in the straw columns compared to the digestate and manure compost columns, with a phospholipid fatty acid derived total microbial biomass 10 x greater than the other biotic columns. Scanning Electron Microscopy imaging shows the most extensive colonisation and biofilm formation on the mineral surfaces in the straw columns. The biotic straw and digestate columns sequester 50 and 14 mg C more than their abiotic controls respectively, while there is no difference in the manure columns. The selection of organic carbon sources to support microbial communities in the flow through bioreactors controlls the silicate weathering rates and CO2 sequestration.

Extracting paleo-weathering signals from authigenic phases in lake sediments: A case-study of Lake Baikal

Authigenic phases in lake sediments hold the potential to record changes in the isotope compositions of past lake water, potentially yielding valuable information on secular changes in continental weathering patterns and rates, including over past glacial cycles.Here, different leaching approaches are investigated with the aim of extracting Sr, Nd, Pb, and Be hosted in authigenic Fe-Mn (oxy)hydroxide sediment phases for precise isotope measurements. Elemental Al/Mn, Ca/Mn, and P/Mn ratios obtained via a mild reductive leach agree well with the composition of marine authigenic Fe-Mn phases. For core top sediments, leached Sr isotope compositions obtained with this leach agree well with the composition of lake water. The Be and Nd isotope compositions of core top leachates are consistent with the spatial variability observed in the water column. Due to high concentrations in Fe-Mn phases, leachate compositions are dominated by authigenic Be, Sr, Nd, and Pb, even in cases when as much as 40% of leached phases (by mass) are non-authigenic. These lines of evidence suggest that the mild reductive leach successfully extracts the modern lake isotope composition from modern sediments in terms of the isotope systems investigated. We further show that the leaching method is also reliable for older sediments (<340 ka): leached paleo-Sr isotope compositions are consistent between the current and previous interglacial periods, as well as for glacial periods. This suggests that reconstructed water isotope compositions are not affected by early diagenetic processes, instead reflecting environmental factors around the lake that determine the composition of weathering fluxes. Although more difficult to assess for Be, Nd, and Pb due to the heterogeneity of modern lake water, the data we present indicate the overall robustness of the leaching approach.These promising results open up lakes as archives for paleo-weathering reconstructions. Given that marine reconstructions face some important limitations (e.g., integration of basin-wide changes in weathering processes, long residence times for Sr, etc.Fe), lake records provide an avenue to improve our understanding of changes in regional weathering processes over glacial-interglacial timescales. The mild reductive leach used here may also be useful for meteoric Be studies in marine shelf settings, to prevent leaching of terrestrial sedimentary Fe-Mn oxy(hydroxide) phases.

Schmidt-hammer R-values from glacially-scoured bedrock surfaces across glacier-foreland boundaries: Insights into Holocene weathering rates with implications for exposure-age dating

Schmidt-hammer R-values were measured on glacially-scoured bedrock outcrops located inside and outside of 11 ‘Little Ice Age’ glacier-foreland boundaries in the Jotunheimen and Jostedalsbreen regions of southern Norway. Analysing paired samples differing in exposure age by ~10,000 years constitutes a field experiment on chemical weathering rates within and between regions. Mean R-values (± 95 % confidence intervals) from inside sites were 65.9 ± 0.6 and 66.9 ± 0.6 for rock surfaces composed of pyroxene-granulite gneiss in Jotunheimen at altitudes of 990–1360 m above sea level and granite and granitic gneiss in the Jostedalsbreen region at 270–620 m a.s.l. The corresponding values from outside sites of 39.9 ± 0.9 and 39.0 ± 0.9 were significantly lower, indicating a higher degree of chemical weathering. In contrast, regional differences in mean R-values were insignificant. A similar pattern is reflected in indices of rock weathering (39.0 % for Jotunheimen and 41.6 % for Jostedalsbreen), and weathering rate (2.8 R-value units and 3.0 units per 1000 years, respectively). These results imply an estimated minimum age resolution of Schmidt-hammer exposure-age dating of ~265–315 years and a maximum age range of ~20,000 years. They suggest potential application of the Schmidt hammer to both studies of weathering rates and exposure-age dating at the regional scale, despite lithological variation associated with different rock types and climatic variation associated with altitudinal differences of up to 1000 m between the sites.

Geochemical Weathering Variability in High Latitude Watersheds of the Gulf of Alaska

AbstractHigh latitude regions across the globe are undergoing severe modifications due to changing climate. A high latitude region of concern is the Gulf of Alaska (GoA), where these changes in hydroclimate undoubtedly affect the hydrogeochemistry of freshwater discharging to the nearshore ecosystems of the region. To fill the knowledge gap of our understanding of freshwater stream geochemistry with the GoA, we compile stream water chemistry data from 162 stream sites across the region. With an inverse model, we estimate fractional contributions to solute fluxes from weathering of silicate, carbonate, and sulfide minerals, and precipitation. We assess weathering rates across the region and compare them against global river yields. The median fractional contribution of carbonate weathering to total weathering products is 78% across all stream sites; however, there are several streams where silicate weathering is a dominant source of solutes. Weathering by sulfuric acid is elevated in glacierized watersheds. Finally, cation weathering rates are lower in GoA streams compared to the world's largest rivers; however, weathering rates are similar when compared to a global dataset of glacier fed streams. We suggest that hydrologic changes driven by glacier ice loss and increased precipitation will alter river water quality and chemical weathering regimes such that silicate weathering may become a more important source of solutes and sulfide oxidation may decrease. This contribution provides a platform to build from for future investigations into changes to stream water chemistry in the region and other high latitude watersheds.

Speed of thermal adaptation of terrestrial vegetation alters Earth's long-term climate.

Earth's long-term climate is driven by the cycling of carbon between geologic reservoirs and the atmosphere-ocean system. Our understanding of carbon-climate regulation remains incomplete, with large discrepancies remaining between biogeochemical model predictions and the geologic record. Here, we evaluate the importance of the continuous biological climate adaptation of vegetation as a regulation mechanism in the geologic carbon cycle since the establishment of forest ecosystems. Using a model, we show that the vegetation's speed of adaptation to temperature changes through eco-evolutionary processes can strongly influence global rates of organic carbon burial and silicate weathering. Considering a limited thermal adaptation capacity of the vegetation results in a closer balance of reconstructed carbon fluxes into and out of the atmosphere-ocean system, which is a prerequisite to maintain habitable conditions on Earth's surface on a multimillion-year timescale. We conclude that the long-term carbon-climate system is more sensitive to biological dynamics than previously expected, which may help to explain large shifts in Phanerozoic climate.

Soil temperature and moisture as key controls of phosphorus export in mountain watersheds

Oligotrophic mountain lakes act as sensitive indicators of landscape-scale changes in mountain regions due to their low nutrient concentration and remote, relatively undisturbed watersheds. Recent research shows that phosphorus (P) concentrations are increasing in mountain lakes around the world, creating more mesotrophic states and altering lake ecosystem structure and function. The relative importance of atmospheric deposition and climate-driven changes to local biogeochemistry in driving these shifts is not well established. In this study, we test whether increasing temperatures in watershed soils may be contributing to the observed increases in mountain lake P loading. Specifically, we test whether higher soil temperatures increase P mobilization from mountain soils by accelerating the rate of geochemical weathering and soil organic matter decomposition. We used paired soil incubation (lab) and soil transplant (field) experiments with mountain soils from around the western United States to test the effects of warming on rain-leachable P concentration, soil P mobilization, and soil respiration. Our results show that while higher temperature can increase soil P mobilization, low soil moisture can limit the effects of warming in some situations. Soils with lower bulk densities, higher pH, lower aluminum oxide contents, and lower ratios of carbon to nitrogen had much higher rain-leachable P concentration across all sites and experimental treatments. Together, these results suggest that mountain watersheds with high-P soils and relatively high soil moisture could have the largest increases in P mobilization with warming. Consequently, lakes and streams in such watersheds could become especially susceptible to soil-driven eutrophication as temperatures rise.

Travertine records climate-induced transformations of the Yellowstone hydrothermal system from the late Pleistocene to the present

Chemical changes in hot springs, as recorded by thermal waters and their deposits, provide a window into the evolution of the postglacial hydrothermal system of the Yellowstone Plateau Volcanic Field. Today, most hydrothermal travertine forms to the north and south of the ca. 631 ka Yellowstone caldera where groundwater flow through subsurface sedimentary rocks leads to calcite saturation at hot springs. In contrast, low-Ca rhyolites dominate the subsurface within the Yellowstone caldera, resulting in thermal waters that rarely deposit travertine. We investigated the timing and origin of five small travertine deposits in the Upper and Lower Geyser Basins to understand the conditions that allowed for travertine deposition. New 230Th-U dating, oxygen (δ18O), carbon (δ13C), and strontium (87Sr/86Sr) isotopic ratios, and elemental concentrations indicate that travertine deposits within the Yellowstone caldera formed during three main episodes that correspond broadly with known periods of wet climate: 13.9−13.6 ka, 12.2−9.5 ka, and 5.2−2.9 ka. Travertine deposition occurred in response to the influx of large volumes of cold meteoric water, which increased the rate of chemical weathering of surficial sediments and recharge into the hydrothermal system. The small volume of intracaldera travertine does not support a massive postglacial surge of CO2 within the Yellowstone caldera, nor was magmatic CO2 the catalyst for postglacial travertine deposition.

Effects of climate and acidic deposition on interannual variations of stream water chemistry in forested watersheds in the Shimanto River Basin, southern Japan

AbstractAlthough the amount of acidic deposition has recently decreased in Japan, it has still deteriorated some forest ecosystems during the past several decades. Moreover, recent climate changes can affect stream water chemistry. We investigated the temporal trend and effects of climate conditions on stream water chemistry for more than 20 years in two areas (Yusuhara and Taisho) in the Shmanto River Basin, southern Japan, where the effects of acidic deposition are considered to be modest. Stream water samples were collected monthly from three forest watersheds selected at each site. The annual means of the stream chemistry were predicted by multiple regression analysis. The ammonium, nitrate, and sulfate concentrations in the bulk precipitation have decreased at Yusuhara, and the sodium, magnesium, calcium, chloride, nitrate, and sulfate concentrations in the stream water have decreased in both areas. The nitrate and sulfate concentrations apparently responded to the decreasing input of acidic deposition. The sunlight hours were positively related with the potassium, magnesium, calcium, nitrate, sulfate, and bicarbonate concentrations in stream water. The results suggest that long sunlight hours boost the photosynthetic activities, thus promoting soil respiration and decomposition of soil organic matter. Moreover, a higher carbonic acid concentration in the soil solution promotes cation weathering and carbonic acid dissociation to bicarbonate. Given the decreasing trends in magnesium and calcium concentration with no change in bicarbonate concentration, we inferred that previousinputs of acidic deposition enhanced the rate of rock weathering.

EVIDENCE OF THE INVOLVEMENT OF STRUCTURAL PREDISPOSITIONS OF THE CRYSTALLINE BASEMENT IN THE OBSERVATION OF MICROEARTHQUAKES IN THE WADI FIRA IN EASTERN CHAD

The seismically active regions of the world are modelled on zones where the crust is constantly evolving, subduction zones or seismically active zones such as the East African Rift. Chad is not one of these zones, because towards the end of the Precambrian, Chad's crustal evolution came to an end and it became part of a stable zone. Nevertheless, micro-earthquakes of up to magnitude four have been recorded in the Wadi-Fira region thanks to the Abéché ABC seismological station. The signals recorded have been processed and located in an area of very uneven high basement at the surface. Their origin is thought to be linked to the dynamics of the aquifer in relation to the rate of weathering, which plays an important role in the infiltration of water, causing the hydrostatic pressure to vary considerably. This variation in pressure can lead to a change in the state of stress in pre-existing faults. An increase in fluid pressure in the rock mass can create fault instability. The largest recorded event is located on the N30°E direction corresponding to the direction of an old non-active fault representing the Volcanic Line of Cameroon.

Hydrochemical and Isotopic Characteristics and the Spatiotemporal Differences of Surface Water and Groundwater in the Qaidam Basin, China

In the context of climate change, precipitation and runoff in the arid inland basins of northwest China have undergone significant changes. The Qaidam Basin (QB) is a typical highland arid inland area. Understanding the spatial and temporal variations in surface water and groundwater chemistry and isotopes, as well as their causes, is crucial for future water resource management and ecological protection. Samples of river, lake, and groundwater, as well as others, were collected and tested in five typical watersheds in the summer and winter. The hydrochemistry and isotopic spatiotemporal differences in various water bodies were studied using the significant difference method, water vapor flux models, hydrochemistry, isotopes, and other methods for cause analyses. The results indicate the following: (1) There are differences in hydrochemistry between the southern and northern basins because the southern basin is more influenced by the dissolution of salt rocks and evaporation, whereas the northern basin is mainly affected by carbonate weathering. (2) The enrichment of δD and δ18O in the northern basin gradually increases from west to east, while in the southern basin, it is the opposite. This is because the southern basin receives a larger contribution of water vapor from the mid-latitude westerlies, while the northern basin primarily relies on local evaporation as its water vapor source. (3) Significant differences are observed in the total dissolved solids (TDS) and hydrochemical types of river water and groundwater between the summer and winter due to higher rates of rock weathering and evaporation in the summer. (4) The more pronounced seasonal differences in hydrogen and oxygen stable isotopes in the southern basin are due to higher rates of internal water vapor circulation in the summer. (5) The similarity in characteristics between river water and groundwater is the result of strong exchanges between river water and groundwater from piedmonts to terminals. The spatiotemporal heterogeneity of terminal lakes is attributed to the accumulation of salts and groundwater replenishment from other sources.

Four volcanically driven climatic perturbations led to enhanced continental weathering during the Late Triassic Carnian Pluvial Episode

The arid climate of the Late Triassic was interrupted by a particularly humid episode known as the Carnian Pluvial Episode (CPE; ca. 234–232 million years ago). The CPE is often linked to eruptions in the Wrangellia Large Igneous Province (LIP), and is assumed to have led to global warming, enhanced weathering, water deoxygenation, and biotic changes. However, direct evidence for a temporal link between volcanic activity and chemical weathering has not yet been established due to the lack of comprehensive records across the CPE. In this study, geochemical and mineralogical analyses are applied to a lacustrine stratigraphic succession of the Jiyuan Basin (North China) that captures the CPE in high resolution. We identify four distinct pulses of enhanced continental chemical weathering characterized by elevated Chemical Index of Alteration values and kaolinite contents. These peaks in continental weathering coincide with Hg/TOC enrichments and negative organic carbon isotope excursions that mark four short (∼400 kyr) but intense pulses of Wrangellia LIP volcanism. In combination with signs of increased humidity, our findings provide direct and independent evidence that Wrangellia LIP eruptions significantly altered CPE chemical weathering rates in response to global warming and wetting. The lake experienced eutrophication and water deoxygenation after each volcanic pulse but the swift recovery of carbon isotopes suggests that the system rapidly returned to conditions prior to the volcanic perturbation. Organic carbon burial facilitated by widespread dysoxic and anoxic waters, and CO2 consumption via enhanced weathering likely played crucial roles in the rapid climatic recovery after each volcanic pulse.

The Chemical Weathering of Rocks and Its Carbon Sink Effect in the Naqu River Basin of the Nujiang River Source Area, Southwest China

Carbon plays an important role in global climate change. The mechanisms of carbon sources and carbon sinks have also received wide attention from society, and the physical and chemical characteristics of riverine ions can reflect the chemical weathering of rocks and carbon sink capacity of river basins. Based on the data on river, rainwater, and rock samples from 2019, this study used various methods, such as ion ratio diagrams and ternary diagrams, to analyze the chemical characteristics of water; the chemical weathering and carbon sink effects of rocks were also calculated while assuming three scenarios based on the main sources of ions in the Naqu River. The results showed that for the whole catchment, the main ion sources in the river were: carbonate rock chemical weathering &gt; silicate rock chemical weathering &gt; evaporite dissolution &gt; atmospheric precipitation input. According to the calculations, in the three scenarios, the carbonate weathering rates were 16.84, 11.32, and 14.08 t/km2/yr, and the carbon sink capacities were 66.47, 121.13, and 93.80 mol/km2/yr, respectively; the evaporite weathering rates were 2.20, 9.63, and 5.92 t/km2/yr, respectively. The silicate chemical weathering rate and carbon sink capacity did not change significantly in either scenario, with 6.82 t/km2/yr and 248.6 mol/km2/yr, respectively. This study quantified the ion sources in the Naqu River basin and accurately analyzed their chemical genesis, which helps in understanding the role of the rivers of the Qinghai–Tibet Plateau in the global carbon cycle and global climate change, in addition to providing a reference for the scientific development of the Nujing River.

Response of Siliceous Marine Organisms to the Permian‐Triassic Climate Crisis Based on New Findings From Central Spitsbergen, Svalbard

AbstractSiliceous marine ecosystems play a critical role in shaping the Earth's climate system by influencing rates of organic carbon burial and marine authigenic clay formation (i.e., reverse weathering). The ecological demise of silicifying organisms associated with the Permian‐Triassic mass extinction is postulated to have elevated marine authigenic clay formation rates, resulting in a prolonged greenhouse climate during the Early Triassic. Yet, our understanding of the response of siliceous marine organisms during this critical interval is poor. Whilst radiolarians experienced the strongest diversity loss in their evolutionary history and perhaps also the greatest population decline of silica‐secreting organisms during this event, only a small number of Griesbachian (post‐extinction) localities that record siliceous organisms are known. Here, we report newly discovered latest Changhsingian to early Griesbachian (Clarkina meishanensis ‐ Hindeodus parvus Zone) radiolarians and siliceous sponge spicules from Svalbard. This fauna documents the survival of a low‐diversity radiolarian assemblage alongside stem‐group hexactinellid sponges making this the first described account of post‐extinction silica‐secreting organisms from the Permian/Triassic boundary in a shallow marine shelf environment and a mid‐northern paleolatitudinal setting. Our findings indicate that latitudinal diversity gradients for silica‐secreting organisms following the mass extinction were significantly altered, and that silica productivity was restricted to high latitude and deep water thermal refugia. This result has potential to further shape our understanding of changes in marine dissolved silica levels and in turn rates of reverse weathering, with implications for our understanding of carbon cycle dynamics during this interval.

Erosional modulation of the balance between alkalinity and acid generation from rock weathering

The balance between alkalinity generation by carbonate and silicate weathering and sulfuric acid generation by sulfide weathering controls the effect of weathering on atmospheric pCO2 over geologic timescales. How this balance varies across environmental gradients remains poorly constrained. Here, we analyze this balance across an erosional gradient of two orders of magnitude in the Three Rivers (Yangtze, Mekong, and Salween Rivers) Headwater Region (TRHR), eastern Qinghai-Tibet Plateau (QTP). By employing major element chemistry and multiple isotopes (δ34SSO4, δ18OSO4, and δ18OH2O) coupled with forward and inverse approaches, we unmix contributions of silicates, carbonates, evaporites, and sulfides to the total weathering budget. Across the TRHR, riverine SO42– is derived mainly from a mixture of an evaporite source with uniform values of δ34SSO4 and δ18OSO4, and a sulfide source that contributes highly variable values of δ34S (−12.2 ‰ to +4.1 ‰) and δ18O (−17.7 ‰ to −1.6 ‰). Contributions of sulfide oxidation to riverine SO42– vary from 16 % to 94 %, and sulfuric acid consumes 6 % to 63 % of the alkalinity produced by weathering. The fractions of weathering alkalinity derived from carbonate weathering range from 36 % to 98 % relative to silicate weathering. The combination of silicate, carbonate, and sulfide weathering suggests that the instantaneous weathering fluxes of most sampled catchments in the TRHR act as a sink of atmospheric CO2 over timescales shorter than marine carbonate burial (∼104 years), but as a carbon source over timescales longer than carbonate burial and shorter than sulfide burial (∼107 years). The spatial variability of the balance between alkalinity and acid generation, and, thus, the relationship between chemical weathering and atmospheric pCO2, are largely dependent on lithology. However, within comparable lithologic settings, sulfide and carbonate weathering rates rise with increasing erosion, whereas silicate weathering rates remain constant. Consequently, plateau weathering shifts from a sink to a source of atmospheric CO2 with increasing erosion. These findings suggest that sulfide weathering is more sensitive to erosion than carbonate and silicate weathering, and that it could play an important role in the long-term carbon cycle during mountain building.

Dynamic redox and nutrient cycling response to climate forcing in the Mesoproterozoic ocean

Controls on Mesoproterozoic ocean redox heterogeneity, and links to nutrient cycling and oxygenation feedbacks, remain poorly resolved. Here, we report ocean redox and phosphorus cycling across two high-resolution sections from the ~1.4 Ga Xiamaling Formation, North China Craton. In the lower section, fluctuations in trade wind intensity regulated the spatial extent of a ferruginous oxygen minimum zone, promoting phosphorus drawdown and persistent oligotrophic conditions. In the upper section, high but variable continental chemical weathering rates led to periodic fluctuations between highly and weakly euxinic conditions, promoting phosphorus recycling and persistent eutrophication. Biogeochemical modeling demonstrates how changes in geographical location relative to global atmospheric circulation cells could have driven these temporal changes in regional ocean biogeochemistry. Our approach suggests that much of the ocean redox heterogeneity apparent in the Mesoproterozoic record can be explained by climate forcing at individual locations, rather than specific events or step-changes in global oceanic redox conditions.

Hydrochemical Characteristics and Controlling Factors in Wudu River Basin of Guizhou Province

TheWudu River is a typical mining-type watershed in the karst mountainous area of western Guizhou Province. Based on the collection of the main stream, tributaries, spring water, and mine water samples in Wudu River Basin, the hydrochemical characteristics and control factors of Wudu River Basin were studied using Gibbs diagram, Piper diagram, and mathematical statistics analysis, and the solute contribution rate of different sources was calculated. The results revealed that the pH value of the water in the Wudu River Basin ranged from 7.87 to 8.52, with an average of 8.14. The TDS values ranged from 135 to 243 mg·L-1, with an average of 191.7 mg·L-1. The major cations in natural river and spring water were Ca2+ and Mg2+, the major anion was HCO3-, and the hydrochemical type was HCO3-Ca. However, owing to the influence of mining activities, the major cations in some tributaries were Ca2+ and Na+, and the hydrochemical types transitioned to HCO3·SO4-Ca and HCO3·SO4-Ca·Na. The ion components of river water in Wudu River Basin were affected by mine water discharge and cation exchange, carbonate rock weathering, silicate rock weathering, and agricultural fertilization. The high concentration of SO42- and Na+in mine water was the primary source of SO42- and Na+in the tributaries of the Wudu River. The method for calculating chemical material balance showed that the contribution rate of carbonate rock weathering ranged from 44.12% to 86.92%, with an average of 74.32%. The contribution rate of mining activities ranged from 3.28% to 37.07%, with an average of 11.61%. Carbonate rock weathering was the main controlling factor of hydrochemical components in the Wudu River Basin; meanwhile, mining activities also had a certain impact on river water chemistry but they showed spatial heterogeneity. The average contribution rates of atmospheric precipitation, silicate rock weathering, agricultural activities, and domestic sewage were 3.75%, 4.67%, 2.85%, and 2.81%, respectively, which had a limited impact on the hydrochemical components of the basin.

Microbial Catalysis for CO2 Sequestration: A Geobiological Approach.

One of the greatest threats facing the planet is the continued increase in excess greenhouse gasses, with CO2 being the primary driver due to its rapid increase in only a century. Excess CO2 is exacerbating known climate tipping points that will have cascading local and global effects including loss of biodiversity, global warming, and climate migration. However, global reduction of CO2 emissions is not enough. Carbon dioxide removal (CDR) will also be needed to avoid the catastrophic effects of global warming. Although the drawdown and storage of CO2 occur naturally via the coupling of the silicate and carbonate cycles, they operate over geological timescales (thousands of years). Here, we suggest that microbes can be used to accelerate this process, perhaps by orders of magnitude, while simultaneously producing potentially valuable by-products. This could provide both a sustainable pathway for global drawdown of CO2 and an environmentally benign biosynthesis of materials. We discuss several different approaches, all of which involve enhancing the rate of silicate weathering. We use the silicate mineral olivine as a case study because of its favorable weathering properties, global abundance, and growing interest in CDR applications. Extensive research is needed to determine both the upper limit of the rate of silicate dissolution and its potential to economically scale to draw down significant amounts (Mt/Gt) of CO2 Other industrial processes have successfully cultivated microbial consortia to provide valuable services at scale (e.g., wastewater treatment, anaerobic digestion, fermentation), and we argue that similar economies of scale could be achieved from this research.