Chemical weathering and CO2 consumption in the glaciated Karuxung River catchment,Tibetan Plateau

Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO₂ balance, it is important to identify the characteristics and driving factors of chemical weathering and CO₂ consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO₂, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km⁻² yr⁻¹, respectively, in maximum) and potential net release of CO₂ (with an upper constraint of 35.6 and 35.2 t km⁻² yr⁻¹, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.     

Chemical weathering and CO2 consumption rate in a multilayered‐aquifer dominated watershed under intensive farming: The Orgeval Critical Zone Observatory,France

The impact of intensive farming on chemical weathering in the Critical Zone is still an open question. Extensively instrumented and monitored over the last 50 years, the Orgeval Critical Zone Observatory (CZO) in France is an observation site impacted by intensive farming since the 1960s. The Orgeval observatory represents an ideal place to study the response and resilience capability of the Critical Zone under agricultural stress. This paper investigates the chemical composition of different water bodies in two nested catchments of the Orgeval CZO, including rainfall, springs, rivers, and rocks, over one and half hydrological year. We show that elemental and strontium isotopic ratios are powerful to constrain the origin of the elements. The results show that the river chemistry at the outlet of the two nested catchments is dominated by rain inputs (particularly atmospheric dust dissolution) and the chemical weathering of limestone and gypsum. Fertilizer input is clearly visible, although the distinction between gypsum dissolution and fertilizer inputs needs more investigation. The mixtures of water masses inferred from our data are in good agreement with the hydrological context of the watershed, that is, a multilayered aquifer structure. At the main outlet of the CZO, we estimate that the input of ocean‐derived solutes through rainfall represents 7 t km^?2 year^?1, on the same order of magnitude as the net fertilizer input (10 t km^?2 year^?1), and that rock weathering releases 50 t km^?2 year^?1. Including previously published physical erosion rates, we estimate that the total denudation rate (physical and chemical) of the Orgeval CZO is 20 mm (1,000 year)^?1, which, along with the entire Seine watershed, is among the lowest chemical denudation rates for carbonate terrains under temperate climate. Chemical denudation is about 10 times higher than physical erosion in the Orgeval CZO. The consumption of CO₂ by rock weathering is estimated to be between 265.10³ and 360.10³ molC km² year^?1, similar for the two nested catchments. Compared with the rivers, the springs show a higher CO₂ consumption rate that suggests, as pointed out earlier, a enhancement of carbonate dissolution linked to nitrification and thus fertilizer application. The hyporheic zone appears to be a hot spot in the carbon cycle at the Orgeval CZO. This study sheds light on the complex, anthropocenic, interplay between geology, climate, and human activities that characterize and that take place in intensive agriculture regions.     

Major ion chemistry of two cratonic rivers in the tropics: Weathering rates and their controlling factors

Continental weathering plays a dominant role in regulating the global carbon cycle, soil chemistry and nutrient supply to oceans. The CO₂-mediated silicate weathering acts as a major CO₂ sink, whereas sulphuric acid-mediated carbonate dissolution releases CO₂ to the atmosphere–ocean system. In this study, dissolved major ions and silica concentrations of two tropical (Damodar and Subarnarekha) river systems from India have been measured to constrain the type and rate of chemical weathering for these basins. The total dissolved solids (TDS) of these rivers, a measure of total solute supply from all possible sources, are about 2–3 times higher than that of the global average for rivers. Mass balance calculations involving inverse modelling estimate that 63 ± 11% of total cations are derived from rock weathering, of which 27 ± 7% of cations are supplied through silicate weathering. The sulphide-S concentrations are estimated by comparing the water chemistry of these two rivers with that of a nearby river (Brahmani) with similar lithology but no signatures of sulphide oxidation. The outflows of Damodar and Subarnarekha rivers receive 17% and 55% of SO₄ through sulphide oxidation, respectively. The sulphide oxidation fluxes from the ore mining areas, such as upper Damodar (0.52 × 10⁹ mol/yr) and lower Subarnarekha (0.66 × 10⁹ mol/yr) basins, are disproportionally (~9 times) higher compared to their fractional areal coverage to the global drainage area. The corresponding CO₂ release rate (2.84 × 10⁴ mol/km²/yr) for the Damodar basin is lower by five times than its CO₂ uptake rate (1.38 × 10⁵ mol/km²/yr). The outcomes of this study underscore the dominance of sulphide oxidation in controlling the dissolved chemical (cationic and sulphur) fluxes.     

粤东五华河流域的化学风化与CO2吸收

基于对粤东五华河干流和支流水体的物理、化学组成测试数据,应用质量平衡法和相关分析法探讨湿热山地丘陵地区岩石化学风化过程对大气CO₂的吸收.结果表明:五华河水体的总溶解性固体含量(77.11 mg/L)接近于世界河流的平均值(65 mg/L);离子组成以Ca²⁺、Na⁺和HCO₃^-为主,可溶性Si次之.五华河流域化学径流组成主要源自硅酸盐矿物化学风化过程的贡献,碳酸盐矿物的贡献较少;大气和土壤CO₂是流域内岩石化学风化的主要侵蚀介质.与同一气候带其他河流相比较,五华河流域岩石化学风化过程对大气CO₂的吸收通量(2.14×105mol/(km²·a))较低,这主要是由于流域内缺乏碳酸盐岩所导致.     

Weathering,Sr fluxes,and controls on water chemistry in the Lake Qinghai catchment,NE Tibetan Plateau

Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and ⁸⁷Sr/⁸⁶Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in ⁸⁷Sr/⁸⁶Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and ⁸⁷Sr/^S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 10⁸ m³/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd.     

A Rb/Sr record of catchment weathering response to Holocene climate change in Inner Mongolia

Variation in the rubidium to strontium (Rb/Sr) ratio of the loess–palaeosol sequences has been proposed to reflect the degree of pedogenesis and weathering in the northwestern region of China. To characterize the Rb/Sr ratio of the dissolved loads of a single catchment, we analysed a 12·08 m sediment core from Daihai Lake in Inner Mongolia, north China. Dating control was provided by ²¹⁰Pb, ¹³⁷Cs and AMS‐¹⁴C. Sequential extraction experiments were conducted to investigate the concentrations of Rb and Sr on various chemical fractions in the lake sediments. Down‐core variation in the Rb/Sr ratios provides a record of Holocene weathering history. From 9 to 3·5 ka bp , accelerated chemical weathering was experienced throughout the Daihai catchment under mainly warm and humid conditions, and this reached a maximum at c. 5 ka bp . However, weathering was reduced between c. 8·25 and 7·90 ka bp , which may reflect the global 8·2 ka cooling event. After c. 2·5 ka bp , increased Rb/Sr ratios with higher frequency of fluctuations indicate reduced weathering within the Daihai catchment. The highest Rb/Sr ratios in the Little Ice Age lake sediments indicate the weakest phase of Holocene chemical weathering, resulting from a marked reduction in Sr flux into the basin. The Rb/Sr record also shows an enhancement of chemical weathering under today's climate, but its intensity is less than that of the Medieval Warm Period. Increased Rb/Sr in lake sediment corresponding to reduced catchment weathering is in striking contrast to Rb/Sr decrease in the glacial loess layers in the loess–palaeosol sequence. Copyright © 2005 John Wiley & Sons, Ltd.     

Direct evidence of the feedback between climate and weathering

Long-term climate moderation is commonly attributed to chemical weathering; the higher the temperature and precipitation the faster the weathering rate. Weathering releases divalent cations to the ocean via riverine transport where they promote the drawdown of CO₂ from the atmosphere by the precipitation and subsequent burial of carbonate minerals. To test this widely-held hypothesis, we performed a field study determining the weathering rates of 8 nearly pristine north-eastern Iceland river catchments with varying glacial cover over 44 years. The mean annual temperature and annual precipitation of these catchments varied by 3.2 to 4.5 °C and 80 to 530%, respectively during the study period. Statistically significant linear positive correlations were found between mean annual temperature and chemical weathering in all 8 catchments and between mean annual temperature and both mechanical weathering and runoff in 7 of the 8 catchments. For each degree of temperature increase, 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. In contrast, annual precipitation is less related to the measured fluxes; statistically significant correlations between annual precipitation and runoff, mechanical weathering, and chemical weathering were found for 3 of the least glaciated catchments. Mechanical and chemical weathering increased with time in all catchments over the 44 year period. These correlations were statistically significant for only 2 of the 8 catchments due to scatter in corresponding annual runoff and average annual temperature versus time plots. Taken together, these results 1) demonstrate a significant feedback between climate and Earth surface weathering, and 2) suggest that weathering rates are currently increasing with time due to global warming.     

Chemical weathering since the Little Ice Age recorded in lake sediments: a high‐resolution proxy of past climate

Because of the different geochemical behaviour of rubidium and strontium in earth surface processes, variations of the Rb/Sr ratios in lake sediments were used as a geochemical proxy of chemical weathering and past climate in a single watershed. Low magnetic susceptibility, low CaCO₃, low Sr concentration and, hence, high Rb/Sr ratio in the lake sediments indicate weak chemical weathering under a cold but wet climate during the Little Ice Age (LIA) in the closed Daihai Lake watershed. The concordant change in both Sr and CaCO₃ concentrations with δ¹⁸O values in the Dunde ice core suggests that weak chemical weathering during the wet LIA was controlled by air temperature. After the LIA, however, precipitation played a dominant role in chemical weathering. Copyright © 2001 John Wiley & Sons, Ltd.     

Annual fossil organic carbon delivery due to mechanical and chemical weathering of marly badlands areas

A key issue in the study of the carbon cycle is constraining the stocks and fluxes in and between C‐reservoirs. Among these, the role and importance of fossil organic carbon (FOC) release by weathering of outcropping sedimentary rocks on continental surfaces is still debated and remains poorly constrained. Our work focuses on FOC fluxes due to chemical and mechanical weathering of marls in two experimental watersheds with typical badlands geomorphology (Draix watersheds, Laval and Moulin, Alpes de Haute Provence, France). Organic matter from bedrock, soil litter and riverine particles are characterized by Rock‐Eval 6 pyrolysis. FOC fluxes due to mechanical weathering are then estimated by monitoring the annual particulate solid exports at the outlets of the watersheds (1985–2005 period). FOC fluxes from chemical weathering were calculated using Ca²⁺ concentrations in dissolved loads (year 2002) to assess the amount of FOC released by the dissolution of the carbonate matrix. Results show that FOC delivery is mainly driven by mechanical weathering, with a yield ranging from 30 to 59 t km^‐2 yr^‐1 in the Moulin (0.08 km²) and Laval (0.86 km²) catchments, respectively, (1985–2005 average). The release of FOC attributed to chemical weathering was 2.2 to 4.2 t km^‐2 for the year 2002. These high FOC fluxes from badlands are similar to those observed in tectonically active mountain catchments. At a regional scale, badland outcropping within the Durance watershed does not exceed 0.25% in area of the Rhône catchment, but could annually deliver 12 000 t yr^‐1 of FOC. This flux could correspond to 27% of the total particulate organic carbon (POC) load exported by the Rhône River to the Mediterranean Sea. At a global scale, our findings suggest that erosion of badlands may contribute significantly to the transfer of FOC from continental surfaces to depositional environments. Copyright © 2012 John Wiley & Sons, Ltd.     

Mass‐balance modeling of mineral weathering rates and CO2 consumption in the forested,metabasaltic Hauver Branch watershed,Catoctin Mountain,Maryland, USA

Mineral weathering rates and a forest macronutrient uptake stoichiometry were determined for the forested, metabasaltic Hauver Branch watershed in north‐central Maryland, USA. Previous studies of Hauver Branch have had an insufficient number of analytes to permit determination of rates of all the minerals involved in chemical weathering, including biomass. More equations in the mass‐balance matrix were added using existing mineralogic information. The stoichiometry of a deciduous biomass term was determined using multi‐year weekly to biweekly stream‐water chemistry for a nearby watershed, which drains relatively unreactive quartzite bedrock. At Hauver Branch, calcite hosts ~38 mol% of the calcium ion (Ca²⁺) contained in weathering minerals, but its weathering provides ~90% of the stream water Ca²⁺. This occurs in a landscape with a regolith residence time of more than several Ka (kiloannum). Previous studies indicate that such old regolith does not typically contain dissolving calcite that affects stream Ca²⁺/Na⁺ ratios. The relatively high calcite dissolution rate likely reflects dissolution of calcite in fractures of the deep critical zone. Of the carbon dioxide (CO₂) consumed by mineral weathering, calcite is responsible for approximately 27%, with the silicate weathering consumption rate far exceeding that of the global average. The chemical weathering of mafic terrains in decaying orogens thus may be capable of influencing global geochemical cycles, and therefore, climate, on geological timescales. Based on carbon‐balance calculations, atmospheric‐derived sulfuric acid is responsible for approximately 22% of the mineral weathering occurring in the watershed. Our results suggest that rising air temperatures, driven by global warming and resulting in higher precipitation, will cause the rate of chemical weathering in the Hauver Branch watershed to increase until a threshold temperature is reached. Beyond the threshold temperature, increased recharge would produce a shallower groundwater table and reduced chemical weathering rates. Copyright © 2013 John Wiley & Sons, Ltd.     

The state of Lake Ladoga pollution by global 90Sr, 137Cs, and 239,240Pu

The state of radioactive pollution of Lake Ladoga has been studied. The purification half-life of lake water from ⁹⁰Sr was found to be 21.7 year. The ratio of ⁹⁰Sr storage in lake water volume to its storage in silts (0?C10 cm layer) was 2: 1. Lake water purification from global ¹³⁷Cs was slower than that from ¹³⁷Cs originating from Chernobyl emergency emission because of the chronic supplement of global ¹³⁷Cs reserve by atmospheric fallouts. The behavior of ⁹⁰Sr, ¹³⁷Cs, and ^239,240Pu in bed soils was in agreement with the geochemical nature of the elements. By the distribution of ^{239, 240}Pu in bed soils, the sedimentation of substances of non-radiation nature was estimated at 0.3 and 0.5 mm/year at denting and flat relief, respectively.     

Characteristics of δ13CDIC in lakes on the Tibetan Plateau and its implications for the carbon cycle

Dissolved inorganic carbon isotope (δ¹³C_DIC) is an important tool to reveal the carbon cycle in lake systems. However, there are only few studies focusing on the spatial variation of δ¹³C_DIC of closed lakes. Here we analyze the characteristics of δ¹³C_DIC of 24 sampled lakes (mainly closed lakes) across the Qiangtang Plateau (QTP) and identify the driving factors for its spatial variation. The δ¹³C_DIC value of these observed lakes varies in the range of ? 15·0 to 3·2‰, with an average value of ? 1·2‰. The δ¹³C_DIC value of closed lakes is close to the atmospheric isotopic equilibrium value, much higher than that in rivers and freshwater lakes reported before. The high δ¹³C_DIC value of closed lakes is mainly attributed to the significant contribution of carbonate weathering in the catchment and the evasion of dissolved CO₂ induced by the strong evaporation of lake water. The δ¹³C_DIC value of closed lakes has a logarithmic correlation with water chemistry (TDS, DIC and pCO₂), also suggesting that the evapo‐concentration of lake water can influence the δ¹³C_DIC value. The δ¹³C_DIC value shows two opposite logarithmic correlations with lake size depending on the δ¹³C_DIC range. This study suggests that the δ¹³C in carbonates in lacustrine sediments can be taken as an indicator of lake volume variation in closed lakes on QTP. Copyright © 2011 John Wiley & Sons, Ltd.     

Temporal variations in Sr and 87Sr/86Sr of the Ganga headwaters: estimates of dissolved Sr flux to the mainstream

The headwaters of the Ganga (the Alaknanda, Bhagirathi and the Ganga) were analysed for their dissolved major ions, Sr and ⁸⁷Sr/⁸⁶Sr on a biweekly to monthly basis over a period of one year to determine their temporal variations and the factors contributing to them. The concentrations of major ions and Sr show significant seasonal variation with lower values during monsoon period in all the three rivers. A similar trend is also observed for ⁸⁷Sr/⁸⁶Sr and Na*/Ca (Na* = Na_r? Cl_r) suggesting relatively lower contribution of Sr and Na from silicates (which are more radiogenic in Sr) during monsoon. Budget calculations show that silicate derived dissolved Sr (Sr_s) in the river Ganga, Alaknanda and the Bhagirathi varied from 10 ± 4 to 27 ± 11, 7 ± 3 to 30 ± 12, 16 ± 6 to 57 ± 23% of measured Sr respectively with lower values during monsoon. The relative decrease in silicate erosion compared to carbonate during monsoon can result from several factors, these include higher dissolution kinetics of the carbonates, lower water–rock interaction time and availability of larger area for weathering. The annual discharge weighted Sr flux derived from the time series data is higher by ～20% from that based on peak flow Sr, and lower by ～40% compared to that derived from lean flow Sr concentration. The area‐normalized annual flux of dissolved Sr from the Ganga at Rishikesh is about five times its flux at Rajshahi (Bangladesh) and a few other major global rivers, such as the Amazon, indicating higher erosion rate over the Himalaya. Copyright © 2010 John Wiley & Sons, Ltd.     

长江中下游湖泊群不同生活型水生植物分布的时空变化(1986—2020年)

不同生活型水生植物对水环境的影响和碳固持能力不同,开展大尺度范围内不同生活型水生植物的时空分布和动态变化研究,是全面掌握湖泊水生态环境变化趋势、准确核算水生生态系统碳源/碳汇的前提。以长江中下游10 km²以上(共131个)的湖泊为研究对象,基于野外调查和先验知识,通过光谱分析,研发了不同生活型水生植物遥感高精度机器学习识别算法,解析了长江中下游湖泊群不同生活型水生植物的时空变化规律。研究表明,长江中下游湖泊群不同生活型水生植物遥感监测精度为0.81,Kappa系数为0.74;1986—2020年长江中下游湖泊群水生植物面积为2541.58~4571.42 km²,占湖泊总面积的15.99%~28.77%,沉水植物是优势类型(Max_1995年=2649.21 km²,Min_2005年=921.38 km²),其次是挺水植物(Max_2005年=1779.44 km²,Min_2020年=569.05 km²)和浮叶植物(Max_2015年=685.68 km²,Min_2000年=293.04 km²);水生植物主要分布在长江干流流域湖泊群,其次是鄱阳湖流域、洞庭湖流域、太湖流域和汉江流域;变化趋势上,1986—2020年长江中下游湖泊群水生植物面积呈现先增长(1986—1995年)、后下降(1995—2010年)、再增加(2010年后)的趋势。本研究可为长江中下游湖泊群生态环境调查及水环境管理提供重要参考。     

Hydrogen emissions from Erebus volcano, Antarctica

The continuous measurement of molecular hydrogen (H₂) emissions from passively degassing volcanoes has recently been made possible using a new generation of low-cost electrochemical sensors. We have used such sensors to measure H₂, along with SO₂, H₂O and CO₂, in the gas and aerosol plume emitted from the phonolite lava lake at Erebus volcano, Antarctica. The measurements were made at the crater rim between December 2010 and January 2011. Combined with measurements of the long-term SO₂ emission rate for Erebus, they indicate a characteristic H₂ flux of 0.03?kg s^–1 (2.8?Mg? day^–1). The observed H₂ content in the plume is consistent with previous estimates of redox conditions in the lava lake inferred from mineral compositions and the observed CO₂/CO ratio in the gas plume (～0.9 log units below the quartz–fayalite–magnetite buffer). These measurements suggest that H₂ does not combust at the surface of the lake, and that H₂ is kinetically inert in the gas/aerosol plume, retaining the signature of the high-temperature chemical equilibrium reached in the lava lake. We also observe a cyclical variation in the H₂/SO₂ ratio with a period of ～10?min. These cycles correspond to oscillatory patterns of surface motion of the lava lake that have been interpreted as signs of a pulsatory magma supply at the top of the magmatic conduit.     

Spatial characteristics and controlling factors of chemical weathering of loess in the dry season in the middle Loess Plateau,China

Hydrochemistry methods were used to decipher the weathering and geochemical processes controlling solute acquisition of river waters in the dry season in the middle Loess Plateau (MLP), one of the most severely eroded areas and turbid riverine systems in the world. River waters were neutral to slightly alkaline with pH varying from 7.6 to 9.6. The total dissolved solids decreased from northwest to southeast with a mean value of 804 mg/l, much higher than the global average and other large rivers in China. Ternary diagram showed that river waters were dominated by Na⁺, HCO₃^?, and Cl^? with the main water‐type of HCO₃^?–Cl^?–Na⁺. Saturation index values, Mg²⁺, Ca²⁺, and HCO₃^? analyses indicated the preferential Ca²⁺ removal by calcite precipitation. Gibbs plots and stoichiometry plots indicated that the dissolved solutes were mainly derived from rock weathering with minor anthropogenic and atmospheric inputs. Samples in the northwestern basin are also influenced by evaporation. A forward model of mass budget calculation showed that, owing to high soluble characteristics, evaporite dissolution was a major feature of river waters and contributed 41% to the total dissolved cations on average, while carbonate and silicate weathering contributed 28%,and 25% on average, respectively. Besides evaporite dissolution, cation exchange is also responsible for the high concentrations of Na⁺ in river water. Spatial variations showed that evaporite dissolution and silicate weathering were higher in the northern basin, whereas carbonate weathering was higher in the southern basin. Different from most rivers in the world, the physical erosion rates (varying from 117.7 to 4116.6 t/km²y) are much higher than the chemical weathering rates (varying from 3.54 to 6.76 t/km²y) in the MLP because of the loose structure of loess and poor vegetation in the basin. In the future, studies on comparison of water geochemistry in different seasons and on influence of different types of land use and soil salinization on water geochemistry, denudation rates, and water quality should be strengthened in the MLP. These results shed some lights on processes responsible for modern loess weathering and also indicate the importance of time‐series sampling strategy for river water chemistry. Copyright © 2016 John Wiley & Sons, Ltd.     

Weak chemical weathering during the Little Ice Age recorded by lake sediments

Low magnetic susceptibility, low Sr content and hence high Rb/Sr ratio in the lake sediment sequence indicate a weak chemical weathering process under arid and cold climate of the Little Ice Age in a single closed lake watershed. According to different geochemical behavior between rubidium and strontium in earth surface processes, variation of Rb/Sr ratios in the lake sediment sequence can be used as an effective geochemical proxy with definite climatic significance of chemical weathering in watershed. Unlike chemical weathering process in tropic zone and modern temperate-humid climate, concordant changes in both Sr content and magnetic susceptibility with δ¹⁸O values of Dunde ice core suggest that the weak chemical weathering was controlled by air temperature during the Little Ice Age maximum. After the Little Ice Age, chemical weathering intensity was controlled also gradually by precipitation with increasing in temperature.     

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

Snowmelt‐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 SO₄^2?. 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.     

CO2 degassing from Pico Island (Azores,Portugal) volcanic lakes

The CO₂ degassing from lakes on Pico Island (Azores archipelago) were characterized in order to estimate the total diffuse CO₂ output and identify the possible sources of CO₂. Two surveys have been made in each lake (Capitão, Caiado, Rosada, Peixinho, Paúl and Seca), in the winter and summer periods. These water bodies show small surface areas and are rather shallow, with depths ranging from 1.8 to 8.6 m. Water samples are cold, both in winter and summer periods, not presenting variations along the water column, with acid to neutral pH (5.26–7.06). The electrical conductivity values point out to very diluted waters (mean range between 27 and 33.4 μS cm⁻¹), of the Na-Cl type, corresponding to meteoric waters influenced by marine salts.To measure the CO₂ flux at the lakes surface the modified accumulation chamber method was used, and a total of 1632 measurements were accomplished (711 in winter surveys and 921 in summer). Two statistical analysis (GSA and sGs) were applied to the results of diffuse CO₂ flux measurements, showing that the CO₂ flux values measured in theses lakes are relatively low (0.60–20.47 g m⁻² d⁻¹), what seems to indicate a single source for CO₂ (biogenic source), also suggested by the water δ¹³C isotopic signature.CO₂ emissions range between 0.04 t d⁻¹ (Rosada_1) and 0.25 t d⁻¹ (Caiado_1) during the winter surveys, being in general similar to the values recorded during the summer surveys that vary between 0.03 t d⁻¹ (Peixinho_2 and Seca_1) and 0.30 t d⁻¹ (Caiado_2). Taken into account the surface area of the lakes, the highest values were estimated for both surveys made in Seca Lake (˜13 t km⁻² d⁻¹). The occurrence of a dense macrophyte mass in a few of the studied lakes, such as Caiado and Seca, seems to enhance the CO₂ flux from these water bodies.     

Chemical characteristics of the crater lakes of Popocatetetl, El Chichon, and Nevado de Toluca volcanoes, Mexico

Three crater lakes from Mexican volcanoes were sampled and analyzed at various dates to determine their chemical characteristics. Strong differences were observed in the chemistry among the three lakes: Nevado de Toluca, considered as dormant, El Chichón at a post-eruptive stage, and Popocatépetl at a pre-eruptive stage. Not surprisingly, no influence of volcanic activity was found at the Nevado de Toluca volcano, while the other volcanoes showed a correlation between the changing level of activity and the evolution of chemical trends. Low pHs (<3.0) were measured in the water from the active volcanoes, while a pH of 5.6 was measured at the Nevado de Toluca Sun lake. Changes with time were observed at Popocatépetl and El Chichón. Concentrations of volcanic-gas derived species like Cl⁻, SO₄²⁻ and F⁻ decreased irregularly at El Chichón from 1983 until 1997. Major cations concentrations also diminished at El Chichón. A 100% increase in the SO₄²⁻ content was measured at Popocatépetl between 1985 and 1994. An increase in the Mg/Cl ratio between 1992 (Mg/Cl=0.085) and 1994 (Mg/Cl=0.177) was observed at Popocatépetl, before the disappearance of the crater lake in 1994. It is concluded that chemical analysis of crater lakes may provide a useful additional tool for active-volcano monitoring.