The chemical composition of meltwater-draining Himalayan glacierized basins reflects the dominance of carbonic acid in weathering of silicate and carbonate minerals, yet the role of sulfuric acid-mediated reactions in the mineral weathering and ionic release is still unclear. Here, we present a long-term study (1992–2018) of chemical weathering characteristics of a precipitation-dominated glacierized basin (Dokriani glacier) of central Himalaya. By using new and reprocessed datasets of major ions from the glacial/subglacial zones of the glacier, we suggest that two-thirds of the dissolved load of the meltwater derives from sulfuric acid-mediated weathering of minerals and rocks. We observed a clear control of carbonic acid-mediated reactions in the early ablation periods, while sulfuric acid-mediated reactions dominate in peak and late ablation periods. The slopes and intercepts in best-fit regressions of [*Ca2+ + *Mg2+ vs *SO42− and HCO3−] and [HCO3− vs *SO42−] in meltwater were following the stoichiometric parameters of sulfide oxidation coupled to carbonate dissolution reactions. The glaciers of the central and western Himalaya are in good agreement with the present estimates. We contend that the bedrock lithology has limited or second-order effects over the ionic release from Himalayan glaciers and surmise that these patterns are broadly applicable to the other orogenic systems of the world.

Knowledge of clay mineralogy is essential for understanding the source areas and weathering environments of fluvial sediments, particularly in large reservoirs facing serious problems with sediment deposition, such as the Three Gorges Reservoir (TGR) in east-central China. The purpose of the present study was to identify the sediment provenances and weathering regimes contributing to the sediment load in the TGR by determining the clay-mineral and geochemical compositions of surface sediments during various seasons. X-ray diffractometry and scanning electron microscopy (SEM) were used to identify the clay minerals. The results showed that illite was the dominant mineral, followed in order by kaolinite, chlorite, and montmorillonite. From a mineralogical perspective, distal sources were the main contributors to the TGR sediments, and regional sources (surrounding tributaries) also contributed much during the three seasons, while proximal sources (hillslope soils) supplied sediment in the flood season but not in the other two seasons. The geochemical and hydrological data generally supported the mineralogical results. In the flood season, the chemical indices of the TGR sediments were >0.4, showing that the sediments contained Al-rich illite minerals and experienced intense hydrolysis. In the other two seasons the TGR sediments were enriched in Fe- and Mg-rich illite minerals, resulting from strong physical weathering. Furthermore, precipitation, rather than air temperature or latitude, was the factor that controlled weathering intensity. These findings provide deep insights into the sediment cycle and chemical weathering in this large reservoir basin.

Secondary surface layers form by replacement of almandine garnet during chemical weathering. This study tested the hypothesis that the kinetic role of almandine’s weathering products, and the consequent relationships of primary-mineral surface texture and specific assemblages of secondary minerals, both vary with the solid-solution-controlled variations in Fe and Al contents of the specific almandine experiencing weathering.

Surface layers are protective (PSL) when the volume of the products formed by replacement is greater than or equal to the volume of the reactants replaced. Under such circumstances, reaction kinetics at the interface between the garnet and the replacing mineral are transport controlled and either transport of solvents or other reactants to, or products from, the dissolving mineral is rate limiting. Beneath PSLs, almandine garnet surfaces are smooth, rounded, and featureless. Surface layers are unprotective (USL) when the volume of the products formed by replacement is less than the volume of the reactants replaced. Under such circumstances, reaction kinetics at the interface between the garnet and the replacing mineral are interface controlled and the detachment of ions or molecules from the mineral surface is rate limiting. Almandine garnet surfaces beneath USLs exhibit crystallographically oriented etch pits. However, contrary to expectations, etch pits occur on almandine garnet grains beneath some layers consisting of mineral assemblages consistent with PSLs.

Based on the Pilling-Bedworth criterion, surface layers are more likely to be protective over a broad range of reactant-mineral compositions when they contain goethite, kaolinite, and pyrolusite. However, this combination requires specific ranges of Fe and Al content of the natural reacting almandine garnet. To form a PSL of goethite and kaolinite, an almandine garnet must have a minimum Al stoichiometric coefficient of ~3.75 a.p.f.u., and a minimum Fe stoichiometric coefficient of ~2.7 a.p.f.u.

Product minerals also influence the mobility of the least-mobile major rock-forming elements. A PSL consisting of goethite, gibbsite, and kaolinite yields excess Al for export during almandine garnet weathering. As the quantity of kaolinite present in the PSL decreases, the amounts of Al available for export increases.

Palaeo-monsoon and palaeoclimate conditions over Southeast Asia are a matter of debate despite notable studies on the continental and oceanic sedimentary record. The present study investigates the environmental magnetic and geochemical records preserved in the deep marine sediments of the northeastern (NE) Arabian Sea to elucidate the erosion history of the western Himalayas and its link with the prevailing hydroclimatic conditions since the late Miocene. For this, the sediment core retrieved during International Ocean Discovery Program (IODP) Expedition 355 at Site U1457 in the NE Arabian Sea has been explored. The results reveal that the hydroclimatic conditions were predominantly arid during the late Miocene, except for humid intervals from 6.1 Ma to 5.6 Ma. Humid climate conditions in the Indus River Basin returned during the mid-Pliocene and continued to the Pleistocene with an intense chemical weathering regime from 1.9 Ma to 1.2 Ma. The dominant sediment source to the NE Arabian Sea at Site U1457 during the late Miocene and the Pliocene was the Indus River, while during the Pleistocene, mixed sediments brought by the Indus River and the Peninsular Indian rivers were observed. The sediment contribution from a chemically less altered mafic source (the Deccan basalts) increased between 1.2 Ma and 0.2 Ma, possibly linked to a weak Indian Summer Monsoon. The summer monsoon wind strength and associated shift in the Inter-Tropical Convergence Zone (ITCZ) influenced the dominant sediment provenance at Site U1457 of the Laxmi Basin.

Long-term climate moderation is commonly attributed to chemical weathering; the greater the temperature and precipitation the faster the weathering rate. To test this widely-held hypothesis, we performed a field study and determined the weathering rates of eight nearly pristine north-east Iceland river catchments with varying glacial cover over 44 y. Statistically significant linear positive correlations were found between mean annual temperature and chemical weathering in all eight catchments and between mean annual temperature and mechanical weathering and runoff in seven of the eight catchments. The runoff, mechanical weathering flux, and chemical weathering fluxes in these catchments are found to increase from 6 to 16%, 8 to 30%, and 4 to 14%, respectively, depending on the catchment for each degree of temperature increase. Positive correlations were found between time and mechanical and chemical weathering for all catchments. In summary, these results demonstrate a significant feedback between climate and Earth surface weathering, and suggest that this weathering rate is currently increasing with time due to global warming.

The composition, morphology and crystal order of clay minerals in silt-sized sediments carried in suspensions from 25 major rivers across tropical southern Africa have been studied by X-ray diffractometry and scanning and transmission electron microscopy. Our goal was to determine the spatial variability of clay-mineral associations in diverse geological settings, and in climatic conditions ranging from humid Angola and Zambia to hyperarid Namibia and the Kalahari. Specific attention was paid to the micromorphology and chemical composition of smectite particles. The relative abundance of smectites, illite/mica, kaolinite and chlorite enabled identification of regions characterized by different physical and chemical processes: (1) negligible chemical weathering is documented in Namibia, where river muds mostly contain illite/mica or smectite derived from Damara metasedimentary or Etendeka volcanic rocks; (2) kaolinite documenting intense weathering, reaches a maximum in the Okavango, Kwando and Upper Zambezi, sourced in subequatorial Angola and Zambia; (3) suspended-load muds in the Limpopo and middle Zambezi catchments display intermediate features, with varied assemblages and smectite compositions reflecting diverse parent lithologies. Clay mineralogy and chemical composition are confirmed as a most effective tool to unravel present and past climatic conditions on a continental scale.

Although loess–paleosol sequences are among the most important records of Quaternary climate change and past dust deposition cycles, few modern examples of such sedimentation systems have been studied. Stratigraphic studies and 22 new accelerator mass spectrometry radiocarbon ages from the Matanuska Valley in southern Alaska show that loess deposition there began sometime after ∼6500 14C yr B.P. and has continued to the present. The silts are produced through grinding by the Matanuska and Knik glaciers, deposited as outwash, entrained by strong winds, and redeposited as loess. Over a downwind distance of ∼40 km, loess thickness, sand content, and sand-plus-coarse-silt content decrease, whereas fine-silt content increases. Loess deposition was episodic, as shown by the presence of paleosols, at distances >10 km from the outwash plain loess source. Stratigraphic complexity is at a maximum (i.e. the greatest number of loesses and paleosols) at intermediate (10–25 km) distances from the loess source. Surface soils increase in degree of development with distance downwind from the source, where sedimentation rates are lower. Proximal soils are Entisols or Inceptisols, whereas distal soils are Spodosols. Ratios of mobile CaO, K2O, and Fe2O3 to immobile TiO2 show decreases in surface horizons with distance from the source. Thus, as in China, where loess deposition also takes place today, eolian sedimentation and soil formation are competing processes. Study of loess and paleosols in southern Alaska shows that particle size can vary over short distances, loess deposition can be episodic over limited time intervals, and soils developed in stabilized loess can show considerable variability under the same vegetation.

The Rb/Sr ratio of lake sediments has been demonstrated to be a potential indicator of chemical weathering by increasing work. However, Rb and Sr in lake sediments are derived from both chemical weathering and physical erosion. Rb and Sr of different forms in lake sediments may record different environmental processes and information. In this study, the variation patterns of Rb and Sr of different forms in sediments of Daihai Lake were investigated. The results show that Rb and Sr of different forms display noticeably different variation patterns due to their different sources and associated environmental processes. Using the Rb/Sr ratios of bulk lake sediments to reflect chemical weathering is not accurate. The non-residual Sr of the sediments without detrital carbonates, representing the Sr leached from the catchment, can be used as an index of chemical weathering because the weathering of Sr minerals is very sensitive to climate change, and the non-residual Sr content of the sediment is determined more by Sr2 + influx than by the physicochemical conditions of lake water. The correspondence between the non-residual Sr and TIC/TOC in Daihai Lake also indicates that the non-residual Sr of the sediments is a good indicator of chemical weathering in the catchment.

Stable isotope analysis along with radiocarbon and luminescence dating of late Pleistocene lacustrine deposits at Burfu in the higher central Himalaya are used to interpret hydrologic changes in the lake basin. From 15.5 ka to ~ 14.5 ka the Burfu lake was largely fed by melting glaciers. A warming event at 14.5 ka suggests an enhanced monsoon and increased carbonate weathering. From ~ 13.5 ka to ~ 12.5 ka the isotopic data suggest large-amplitude climate variability. Following this, the isotope data suggest a short-lived, abrupt cooling event, comprising a ~ 300-yr intense cool period followed by a ~ 500-yr interval of moderate climate. A shift in isotope values at ~ 11.3 ka may signify a strengthening monsoon in this region. The inferred climatic excursions appear to be correlative, at least qualitatively, with global climatic events, and perhaps the Burfu lake sequence provides regional evidence of globally recorded excursions. This study also suggests a potential use of radiocarbon ages in specific environments as a paleoenvironmental proxy.

The lowland savannas (Llanos) of Colombia and Venezuela are covered by extensive aeolian landforms for which little chronological information exists. We present the first optically stimulated luminescence (OSL) age constraints for dunes in the Llanos Orientales of lowland Colombia and new ages for dunes in the Venezuelan Llanos. The sampled dunes are fully vegetated and show evidence of post-depositional erosion. Ages range from 4.5 ± 0.4 to 66 ± 4 ka, with the majority dating to 27–10 ka (Marine Isotope Stage 2). Some dunes accumulated quickly during the last glacial maximum, although most were active 16–10 ka. Accretion largely ceased after 10 ka. All dunes are elongated downwind from rivers, parallel with dry season winds, and are interpreted as source-bordering features. As they are presently isolated from fluvial sediments by gallery forest it is proposed that activity was associated with a more prolonged dry season, which restricted gallery forest, leading to greater sediment availability on river shorelines. Such variability in dry season duration was potentially mediated by the mean latitude of the ITCZ. The cessation of most dune accretion after ca. 10 ka suggests reduced seasonality and a more northerly ITCZ position, consistent with evidence from the Cariaco Basin.

High-resolution siliciclastic grain size and bulk mineralogy combined with clay mineralogy, rubidium, strontium, and neodymium isotopes of Core MD01-2393 collected off the Mekong River estuary in the southwestern South China Sea reveals a monsoon-controlled chemical weathering and physical erosion history during the last 190,000 yr in the eastern Tibetan Plateau and the Mekong Basin. The ranges of isotopic composition are limited throughout sedimentary records: 87Sr/86Sr = 0.7206–0.7240 and ε Nd(0) = −11.1 to −12.1. These values match well to those of Mekong River sediments and they are considered to reflect this source region. Smectites/(illite + chlorite) and smectites/kaolinite ratios are used as indices of chemical weathering rates, whereas the bulk kaolinite/quartz ratio is used as an index of physical erosion rates in the eastern Tibetan Plateau and the Mekong Basin. Furthermore, the 2.5–6.5 μm/15–55 μm siliciclastic grain size population ratio represents the intensity of sediment discharge of the Mekong River and in turn, the East Asian summer monsoon intensity. Strengthened chemical weathering corresponds to increased sediment discharge and weakened physical erosion during interglacial periods. In contrast, weakened chemical weathering associated with reduced sediment discharge and intensified physical erosion during glacial periods. Such strong glacial–interglacial correlations between chemical weathering/erosion and sediment discharge imply the monsoon-controlled weathering and erosion.

The lightness (L*) and concentrations of Rb, Sr and organic carbon (C org) have been measured in the age-constrained lake sediment cores recovered from Co Ngoin in the central Tibetan Plateau. Dissolved Sr flux is a dominant control on the variation of Rb/Sr ratios in the sediments. Variations in color and geochemical proxies of Co Ngoin sediments display a continuous history of late glacial to mid-Holocene chemical versus physical weathering intensity in response to past climatic changes between approximately 13,500 and 4500 cal yr B.P. A lower chemical weathering under a late glacial climate was followed by a higher weathering during the Holocene Optimum. Weathering intensity in the central Tibetan Plateau catchment also responds to well-known climatic events, such as the Younger Dryas (YD), and possibly the Holocene Event 5 (HE-5). Although there are differences in time or duration of the climatic events, many of the well-known late glacial to mid-Holocene events occurred in high-elevation Co Ngoin where atmospheric circulation might play a hemispherical role in climatic forcing. The sediment hiatus since c. 4200 14C yr B.P. in the Co Ngoin indicates a period of desiccation that was probably associated with a sharp decrease in summer monsoon strength. Our lascustrine results not only imply catchment weathering variations in response to late glacial to mid-Holocene climatic conditions in the central plateau, but also provide further evidence for global connections between regional climates.

The Triassic–Jurassic rift-valley stage of Tethyan rifting in the Western-Central Mediterranean area is characterized by a development of a puzzle of plates and microplates with the deposition of continental redbeds (in the internal domains of the Gibraltar Arc and Calabria–Peloritani Arc) that can be considered a regional lithosome. This paper aims to reconstruct the chemical weathering conditions of the Triassic–Jurassic boundary in the Western-Central Mediterranean area using the geochemical and mineralogical composition of continental redbed mudrocks of Mesozoic age. The mudrocks from the Calabria–Peloritani Arc show higher values of weathering (mobility) indices (αMg=(Al/Mg)sed/(Al/Mg)UCC; αK=(Th/K)sed/(Th/K)UCC; αBa=(Th/Ba)sed/(Th/Ba)UCC) than the Gibraltar Arc samples. Furthermore, the CIA (Chemical Index of Alteration) and MIA (Mineralogical Index of Alteration) values and the ‘Rb-type indices’ (e.g. Rb/Sr and Rb/K ratios) are higher for the Calabria–Peloritani Arc mudrocks than the Gibraltar Arc samples. All these geochemical proxies closely resemble each other and show similar variations suggesting climatic changes towards humid conditions through the Uppermost Triassic to Lowermost Jurassic that favoured chemical weathering conditions. This period is probably characterized by seasonal climate alternations corresponding to an increase in palaeoclimatic humidity. The mineralogical compositions of the Mesozoic mudrocks further confirm these indications as shown by a higher abundance of kaolinite, related to warm–humid conditions, in the Calabria–Peloritani Arc mudrocks than in those of the Gibraltar Arc.

Comprehensive geochemical analyses (bulk parameters, major and trace elements, organic matter, mineralogy and particle analysis) were carried out on sediments from seven lakes on Fildes Peninsula, King George Island. The resulting compositional dataset was subjected to principal component analysis and cluster analysis. The results showed that four different lacustrine sedimentary environments can be distinguished: i) lakes 1 and 2 with relatively high values of secondary aluminous clay minerals, ii) lake 4 with anthropogenic enrichment of Co, Cu and Zn, iii) lake 7 with relatively high values of Ba and P and a high zeolite content, and iv) all the other studied lakes. Our results indicate moderate chemical weathering in all lacustrine sediments and that the distance to the glacial ice margin is one of the most important factors influencing the chemical weathering in the area. Furthermore, depositional processes have little influence on the geochemistry of the investigated elements and that local bedrock is the main source of sediments in the lakes on Fildes Peninsula.

We have explored chemical weathering of probable martian materials at low temperatures based on the increasing evidence for non-hydrothermal water at or near the martian surface. Chemical weathering of minerals at low temperatures (as low as 0 °C) in aqueous environments on Mars can provide geochemical energy to support construction of potential martian organisms. Here, we examine the geochemical energy available from the interaction of the martian surface or near-surface materials with low-temperature water. We calculate the Gibbs free energy for 13 different weathering reactions that are likely to be important on Mars. The aqueous weathering of 1 kg of an ultramafic rock such as the Chassigny meteorite under present martian conditions can support the construction of ~30 g of microbes. The aqueous weathering of 1 kg of a basaltic rock on Mars can support the construction of ~26 g of biomass under present martian conditions and ~32 grams for conditions probable in the past. This means that ~1.3×1019 g of potential biomass could have been supported from weathering a global layer of rock 1 m thick. Thus, low-temperature water–rock reactions on Mars can produce abundant geochemical energy for potential martian microbes.