Silicic Research Articles

Impacts of wastewater treatment plant effluents on dissolved inorganic carbon in highly urbanized karst rivers, Southwest China

Wastewater treatment plants (WWTPs) are an important manifestation of the impact of urbanization on aquatic ecosystems, and the influences of effluents discharge from WWTPs on receiving river carbon biogeochemical cycle processes has been a research hotspot. However, our knowledge about potential impacts of WWTP effluents on dissolved inorganic carbon (DIC) cycle in karst rivers is rather limited. This study investigates the water chemistry and carbon isotope composition (δ13CDIC) in the urbanized reach of a river that drains the world’s largest continuous karst region in Southwest China, in an attempt to determine the effects of WWTP effluents on karst river DIC cycle and source discrimination. The results reveal: (1) Partial pressure of dissolved carbon dioxide (pCO2) levels in the river increased noticeably during the dry and normal seasons after receiving WWTP effluents; (2) There existed an ionic ratio overlap between end-members of silicate rock weathering and WWTP effluents which requires caution in identifying end-members of rock weathering in urbanized karst rivers; (3) DIC in the highly urbanized karst rivers was affected by complex geochemical processes and these processes varied in different seasons; (4) The contribution of WWTP effluents to the riverine DIC pool was 21±13 %, 58±21 % and 66±33 % in the wet, dry, and normal seasons, respectively. These findings highlight the interference of WWTP effluents with DIC carbon cycling in the receiving karst rivers. Since DIC from WWTPs do not relate with consuming atmospheric or soil CO2, it is important to exclude their contribution from the watershed’s rock weathering carbon sink budget. Based on these findings, we insist that the role and effect of WWTP effluents should be carefully considered when examining DIC carbon source and cycling in rivers that drain urbanized watersheds with abundant wastewater treatment plants.

Chemical weathering and CO2 consumption rates of the Koshi River Basin: modelling and quantifying

The Koshi River is a typical river originating from the Tibetan Plateau that drains into the Indian Plain. To quantify the chemical weathering and CO2 consumption rates of the upstream alpine meltwater-supplied mountainous and downstream rainfall-impacted temperate plain regions, 46 river water samples were collected at 23 sites during monsoon and post-monsoon seasons, and major ions concentrations were measured in the laboratory. The forward model was applied to calculate carbonate weathering rate (CWR), silicate weathering rate (SWR), and their CO2 consumption rates ([CO2]car and [CO2]sil). For investigating the hydrological impacts, correlation analysis was applied between the chemical weathering rates and different runoff components based on the Spatial Process in Hydrology model at each sampling site. Results show that carbonate and silicate rock weathering control the river water chemistry. The average silicate weathering rate is 7.37 tons/km2/yr, consuming 3.40 × 105 mol/km2/yr CO2 while considering sulfide-involved carbonate weathering, the carbonate weathering rate is 26.35 tons/km2/yr, consuming 3.82 × 105 mol/km2/yr CO2. Overall, chemical weathering and CO2 consumption rates are enhanced in monsoon season in both the upstream and downstream regions owing to the intense hydrological cycle. These rates are relatively higher in the alpine upstream region during the post-monsoon season due to intense physical erosion, and higher in downstream during the monsoon season due to the greater volume of water. The significant positive correlations between snowmelt runoff with CWR and [CO2]car indicated that the rising precipitation and temperature leading to enhanced snowmelt would increase the carbonate weathering rate. Hence, this study provides a valuable understanding of the spatiotemporal variations in river hydrochemistry and the role of hydrology in shaping chemical budget within the snow and glacier-fed Himalaya River Basins.

Trace element geochemistry of carbonatites and associated alkaline rocks of Mundwara Igneous complex, Sirohi district, Rajasthan, India

Carbonatites are widely recognized for their potential to host significant deposits of rare earth elements (REEs) and other rare metals. These igneous rocks, characterized by their high carbonate mineral content, are often rich in REEs, niobium, tantalum, and other valuable elements. This makes carbonatites key targets for mining and exploration. Carbonatites are believed to form from either primary carbonate magma derived directly from the mantle or from secondary melts. These secondary melts can originate from carbonated silicate magmas through liquid immiscibility or from the residual melts resulting from the fractional crystallization of silicate magmas. The coexistence of carbonatites and alkaline silicate rocks in most complexes, their coeval emplacement in many, and overlapping initial 87Sr/86Sr ratios supports the theory of their cogenesis. In this study, we aim to investigate the trace element geochemistry of carbonatites and coeval alkaline silicate rocks from the Mundwara Igneous Complex, Sirohi district, Rajasthan in India. Our trace element data indicate that the carbonatites and alkaline silicate rocks in this complex are products of fractional crystallization from two separate parental melts, formed through liquid immiscibility of a carbonated alkaline silicate magma.

Paleoenvironmental reconstruction of a Neogene diatomite deposit from La Pampa Province (Argentina)

Diatomite deposits constitute siliceous biogenic sedimentary rocks primarily composed of diatoms. In Argentina, there is a scarcity of paleoenvironmental reconstructions for these deposits. This study focuses on the analysis of the diatom content in a Plio-Pleistocene diatomite from La Pampa Province. The aim is to identify diatom diversity and reconstruct the evolution of paleoenvironments. The studied section of 4.40 m is located at the CP site (38°08′40.5′’S; 67°09′23.2′’W, El Sauzal Formation). The profile is a laminated white diatomite with three levels of volcanic ash. Seven samples 50 cm-equidistant were extracted and oxidized with H2O2 for diatom analysis. 500 valves/slide were counted in order to calculate relative abundances. Diatom zones were defined using CONISS. The analysis revealed 72 morphospecies, with 28 of them exhibiting abundances > 4%. The diatom flora is predominantly composed of small fragilarioid diatoms accompanied by Discostella, Aulacoseira, Epithemia, Rhopalodia, and Cymbella species, indicating a lacustrine origin. At the base, a paleolake with a relatively alkaline pH, low nitrogen concentrations and high phosphates (volcanic ash) favored the growth of a diverse diatom community. Towards the top, the dominance of fragilarioids, the decrease in freshwater planktonic taxa and the presence of gypsum suggest a shallower environment with increased salinity during the drier periods of the Plio-Pleistocene.

Enhanced silicate weathering accelerates forest carbon sequestration by stimulating the soil mineral carbon pump.

Enhanced silicate rock weathering (ERW) is an emerging strategy for carbon dioxide removal (CDR) from the atmosphere to mitigate anthropogenic climate change. ERW aims at promoting soil inorganic carbon sequestration by accelerating geochemical weathering processes. Theoretically, ERW may also impact soil organic carbon (SOC), the largest carbon pool in terrestrial ecosystems, but experimental evidence for this is largely lacking. Here, we conducted a 2-year field experiment in tropical rubber plantations in the southeast of China to evaluate the effects of wollastonite powder additions (0, 0.25, and 0.5 kg m-2) on both soil organic and inorganic carbon at 0-10 cm depth. We found that ERW significantly increased the concentration of SOC and HCO3 -, but the increases in SOC were four and eight times higher than that of HCO3 - with low- and high-level wollastonite applications. ERW had positive effects on the accrual of organic carbon in mineral-associated organic matter (MAOM) and macroaggregate fractions, but not on particulate organic matter. Path analysis suggested that ERW increased MAOM mainly by increasing the release of Ca, Si, and Fe, and to a lesser extent by stimulating root growth and microbial-derived carbon inputs. Our study indicates that ERW with wollastonite can promote SOC sequestration in stable MOAM in surface soils through both the soil mineral carbon pump and microbial carbon pump. These effects may have been larger than the inorganic CDR during our experiment. We argue it is essential to account for the responses of SOC in the assessments of CDR by ERW.

An Analytical Method for Quantification of Sn Isotope Variations in Geological Materials Using MC‐ICP‐MS

A robust analytical method is presented here, for measurements of Sn isotope variations with high precision using a multi‐collector inductively coupled plasma‐mass spectrometer (MC‐ICP‐MS). A silicate rock dissolution procedure was used, together with means to remove organic matter introduced by the resin during ion‐exchange chromatography. The two‐stage ion exchange chromatography efficiently isolates Sn from the matrix and isobarically interfering elements, from samples with variable Sn mass fractions (~ 0.03 to 7 μg g−1). A double spike technique was also implemented to correct any secondary mass bias induced during sample processing and isotope ratio measurements. An intermediate precision (2s) of ± 0.47 was obtained for ε122/118Sn (using internal normalisation; n = 70 over a period of 29 months), ± 0.021‰ for δ122/118Sn (using double spike; n = 176 over a period of 29 months) and ± 0.059‰ for δ122/118Sn (using Sb doping; n = 34 over a period of 4.5 months) for the Sn standard solution, NIST SRM 3161a (Lot# 140917). The δ122/118SnNIST SRM 3161a of eleven geological reference materials are reported for the first time (BIR‐1a, BRP‐1, DTS‐2b, ECRM 782‐1, JP‐1, OKUM, QLO‐1a, RGM‐2, SGR‐1b, STM‐2 and UB‐N), with five others (AGV‐2, BCR‐2, BHVO‐2, GSP‐2 and W‐2a) showing similar results to previous studies, generally with improved precision. The intermediate precision (2s) of replicate dissolutions of ten RMs (AGV‐2, BCR‐2, BHVO‐2, BIR‐1a, DTS‐2b, GSP‐2, OKUM, SGR‐1b, STM‐2 and W‐2a) varied from 0.003 to 0.054‰. Typical repeatability precision (2SE) of individual measurements of these ten RMs over multiple measurement sessions varied from 0.031 to 0.297‰ (with 120Sn+ beam intensity < 2.37 V) and 0.017 to 0.025‰ (with 120Sn+ beam intensity > 2.37 V).

Earliest evidence of human occupations and technological complexity above the 45th North parallel in Western Europe. The site of Lunery-Rosieres la-Terre-des-Sablons (France, 1.1 Ma)

The site of LuneryRosieres la-Terre-des-Sablons (Lunery, Cher, France) comprises early evidence of human occupation in mid-latitudes in Western Europe. It demonstrates hominin presence in the Loire River Basin during the Early Pleistocene at the transition between an interglacial stage and the beginning of the following glacial stage. Three archaeological levels sandwiched and associated with two diamicton levels deposited on the downcutting river floor indicate repeated temporary occupations. Lithic material yields evidence of simple and more complex core technologies on local Jurassic siliceous rocks and Oligocene millstone. Hominins availed of natural stone morphologies to produce flakes with limited preparation. Some cores show centripetal management and a partially prepared striking platform. The mean ESR age of 1175 ka ± 98 ka obtained on fluvial sediments overlying the archaeological levels could correspond to the transition between marine isotopic stages (MIS) 37 and 36, during the normal Cobb Mountain subchron, and in particular at the beginning of MIS 36. The Lunery site shows that hominins were capable of adapting to early glacial environmental conditions and adopting appropriate strategies for settling in mid-latitude zones. These areas cannot be considered as inhospitable at that time as Lunery lies at some distance from the forming ice cap.

Reduced accrual of mineral-associated organic matter after two years of enhanced rock weathering in cropland soils, though no net losses of soil organic carbon

Enhanced rock weathering (ERW), the application of crushed silicate rock to soil, can remove atmospheric carbon dioxide by converting it to (bi) carbonate ions or solid carbonate minerals. However, few studies have empirically evaluated ERW in field settings. A critical question remains as to whether additions of crushed rock might positively or negatively affect soil organic matter (SOM)—Earth’s largest terrestrial organic carbon (C) pool and a massive reservoir of organic nitrogen (N). Here, in three irrigated cropland field trials in California, USA, we investigated the effect of crushed meta-basalt rock additions on different pools of soil organic carbon and nitrogen (i.e., mineral-associated organic matter, MAOM, and particulate organic matter, POM), active microbial biomass, and microbial community composition. After 2 years of crushed rock additions, MAOM stocks were lower in the upper surface soil (0–10 cm) of plots with crushed rock compared to unamended control plots. At the 2 sites where baseline pre-treatment data were available, neither total SOC nor SON decreased over the 2 years of study in plots with crushed rock or unamended control plots. However, the accrual rate of MAOM-C and MAOM-N at 0–10 cm was lower in plots with crushed rock vs. unamended controls. Before ERW is deployed at large scales, our results suggest that field trials should assess the effects of crushed rock on SOM pools, especially over multi-year time scales and in different environmental contexts, to accurately assess changes in net C and understand the mechanisms driving interactions between ERW and SOM cycling.

Hydrochemical and Formation Mechanism Studies of Groundwater in Quaternary Aquifer in a Northern Plain of China: An Example of Beijing Plain

Beijing Plain is a very active part of Beijing city regarding the socio-economic and human activities of the region. Over the past four decades, Beijing’s economic development and the continuous drought for nearly 10 years in the 2000s have negatively impacted the groundwater quantity and quality. Therefore, it is necessary to investigate the present situation of groundwater chemistry in this region to develop a comprehensive database and orientation for future research on groundwater quality evaluation. Mathematical statistics, Piper’s trilinear diagram, Gibbs plots, the ion ratio method and PHREEQC software 3.7.3 were used to analyze the groundwater hydrogeochemical characteristics and formation mechanisms of the quaternary aquifers of the Beijing Plain area. Hydrogeochemical results indicated that the groundwater is slightly alkaline, with pH values ranging from 6.76 to 8.65 and an average value of 7.92. The order of major cations in groundwater was Ca2+ > Na+ > Mg2+ > K+ with average values of 66.54 mg/L, 50.58 mg/L, 23.78 mg/L, and 1.81 mg/L, respectively, while the order of major anions was HCO3− > SO42− > Cl− with average values of 284.89 mg/L, 52.1 mg/L and 35.5 mg/L, respectively. The groundwater chemical types are Mg-Ca-Cl-HCO3, Na-Ca-HCO3, Mg-Ca-HCO3 and Mg-Na-HCO3. Research on the main influencing factors and PHREEQC hydrogeochemical inverse simulations results along the four pathways selected confirmed that rock weathering with sulfate, silicate and carbonate rock mineral dissolution and Na+, Mg2+ and Ca2+ ion reaction exchange influenced groundwater hydrogeochemical characteristics of the quaternary aquifers of the Beijing Plain area. Understanding the formation mechanisms of hydrogeochemistry in quaternary plains provides guidance for future studies and, through suggestions and case studies, facilitates decision-making by policy-makers on the sustainable management of groundwater resources.

Hydrochemical Characteristics and Controlling Factors of the Mingyong River Water of the Meili Snow Mountains, China

The hydrochemical characteristics of rivers are affected by many natural factors, such as the nature of watershed bedrock, watershed environment, vegetation, and human activities. Examining the hydrochemistry of a river can provide insights into the baseline hydrological conditions, the geochemical environment, and the overall water quality of the river. In order to examine the hydrochemical characteristics and controlling factors of the water in the Mingyong River, a total of 154 water samples were gathered from the glacier meltwater, midstream, and downstream regions. Firstly, the findings revealed that the dominant cations are Ca2+ and Mg2+, while the dominant anions are HCO3− and SO42−. The mass concentration order of cations is Ca2+ > Mg2+ > Na+ > K+, and for anions, it is HCO3− > SO42− > NO3− > Cl−. The average concentration of TDS in the river water is 81.69 mg·L−1, with an average EC of 163.63 μs·cm−1 and an average pH of 8.99. Temporal variations in ion concentrations exhibit significant disparities between the glacier melting and accumulation periods. High ion concentration values are primarily observed during the glacier accumulation period, while values decrease during the glacier melting period due to increased precipitation. The river water in the study region is categorized as (HCO3− + SO42−)-(Ca2+ + Mg2+) type. Secondly, the Pearson correlation analysis indicates clear relationships between different parameters, indicating that the major ions were mostly influenced by materials from the Earth’s crust. The primary principal source of solutes in the water of the Mingyong River is rock weathering. The cations and anions present in the river water are derived from the breakdown of carbonate rocks and the dissolving of substances from silicate rocks. However, the influence of carbonate rocks is more significant compared to that of silicate rocks. Finally, the Mingyong River water is suitable for agricultural irrigation with minimal land salinization damage, making it appropriate for agricultural purposes but not suitable for people and animals to drink from directly.

Application of MARS-5 and UltraWAVE Microwave Systems to the Digestion of Silicate Rocks Followed by ICP-MS Analysis

Application of MARS-5 and UltraWAVE Microwave Systems to the Digestion of Silicate Rocks Followed by ICP-MS Analysis

Compositional nutrient analysis of greenhouse grown ryegrass (Lolium multiforum) fertilized with raw and hydrothermal-treated igneous rock as diagnostic tool for balanced fertilization in tropical environments

Due to the escalating demand for conventional potassium sources, and their unavailability in many African countries, there is a growing interest in hydrothermally treated igneous rocks as viable alternatives. These materials exhibit promising potential in enhancing potassium release, comparable to traditional sources like muriate of potash (M.O.P.). However, it remains uncertain whether they can adequately fulfill the nutrient requirements of plants. In this study, we evaluated nutrient balance in ryegrass (Lolium multiflorum) using raw and hydrothermally treated K-bearing silicate rocks as fertilizers. The Compositional Nutrient Diagnostic (CND) approach was used to assess the plants’ nutrient status, involving identification of high-yield subpopulations, and setting a yield cutoff. We derived a theoretical threshold for nutrient imbalance (CNDr2) using statistical methods like the chi-square distribution function and low-yield subpopulation proportion. CNDr2 was validated via Cate–Nelson partition and sum of squared individual nutrient indexes. Results showed a yield cutoff of 37.759 kg ha−1, distinguishing low-yield and high-yield subpopulations based on cumulative variance ratio functions from survey data. The theoretical threshold derived using the chi-square function was 10.1, subsequently validated by the Cate–Nelson method. Critical CND nutrient indices were symmetrical around zero, but their sum indicated foliar nutrient imbalance, notably zinc, potassium, and copper excess, attributed to 20 interactions identified (4 synergetic and 16 antagonistic). This study underscores hydrothermal treatment’s efficacy in improving nutrient availability and achieving a balanced nutrient profile compared to raw materials. It offers a promising solution for enhancing agricultural productivity, especially in tropical regions like Africa, where traditional sources are scarce.

Critical Raw Materials Supply: Challenges and Potentialities to Exploit Rare Earth Elements from Siliceous Stones and Extractive Waste

Critical raw materials (CRMs) supply is a challenge that EU countries have to face, with many thinking about domestic procurement from natural ore deposits and anthropogenic deposits (landfills and extractive waste facilities). The present research focuses on the possibilities linked to the supply of CRMs and the potential for exploiting rare earth elements (REEs), investigating a large variety of extractive waste and siliceous rocks in the Piedmont region (Northern Italy). Indeed, the recovery of REEs from the extractive waste (EW) of siliceous quarries and other siliceous ore deposits can be a valuable way to reduce supply chain risks. Starting with a review of the literature on mining activities in Piedmont and continuing with the sampling and geochemical, mineralogical, petrographic, and environmental characterization of EW facilities connected to siliceous dimension stones, of kaolinitic gneiss ore deposits, and of soils present near the investigated areas, this study shows that the degree of REEs enrichment differs depending on the sampling area (soil or EW) and lithology. The concentration of REEs in the EW at some sampling sites fulfils the indicators of industrial-grade and industrial recovery; the high cumulative production and potential market values of EW and the positive recovery effects through proven methodologies indicate a viable prospect of REE recovery from EW. However, REE recovery industrialization faces challenges such as the difficulty in achieving efficient large-scale recovery due to large regional differences in REE abundance, the mismatch between potential market value and waste annual production, etc. Nonetheless, in the future, EW from dimension stone quarries could be differentially studied and reused based on the enrichment and distribution characteristics of trace elements. The present paper shows investigation procedures undertaken to determine both CRMs potentialities and environmental issues (on the basis of literature data employed to select the more-promising areas and on sampling and characterization activities in the selected areas), together with procedures to determine the waste quantities and tentative economic values of REEs present in the investigated areas. This approach, tested on a large area (Piedmont region), is replicable and applicable to other similar case studies (at EU and non-EU levels) and offers decision makers the possibility to acquire a general overview of the potential available resources in order to decide whether and where to concentrate efforts (including economic ones) in a more detailed study to evaluate the exploitable anthropogenic deposits.

Unexpected contributions by carbonates and organic matter in a silicate-dominated tropical catchment: An isotope approach

The understanding of global carbon has rarely extended to small-scale tropical river basins. To address these uncertainties, this study aims to investigate the importance of rock weathering and organic matter turnover in the carbon cycle in a terrain dominated by crystalline silicate rocks. The geochemical composition of the dissolved and particulate carbon phases (DIC, DOC and POC) and their stable carbon isotopes were studied in the Deduru Oya River in Sri Lanka. Dissolved inorganic carbon (DIC) was the most dominant carbon phase and its contribution to the total carbon pool varied between 67 and 89 %. Furthermore, the δ13CDIC values in the river varied between −1.1 and −16.5 ‰. The lithological characteristics and molar ratios between Ca2+, Mg2+ and HCO3− indicated rock weathering mainly by CO2 and carbonic acid. The δ13CDIC values for groundwater input were −15.9 ‰, while for carbonate weathering, mainly due to fertiliser input, they reached a value of −12.7 ‰. This input was fed into an isotope mass balance to determine the relative contributions. However, the isotope mass balance was only plausible after correcting for the effects on δ13CDIC caused by degassing and photosynthesis. Our study demonstrated that carbonate weathering and organic matter turnover are essential components of the river carbon cycle even in a silicate dominated catchment. They can represent up to 60 % of the DIC pool. Combined with the higher organic matter turnover and high pCO2 in the river water, it can be suggested that the Deduru Oya River acts as a net source of CO2 in the atmosphere. Our study shows that CO2 degassing and in-stream photosynthesis in tropical river systems need to be considered along with chemical weathering to account for carbon transport and turnover in tropical rivers.

Water chemical formation mechanism and water quality analysis of Shichuan River under the influence of human activities

ABSTRACT It is necessary to analyze the characteristics of the water environment and factors influencing the basin in order to determine its current ecological status. This study aims to investigate the chemical properties in the Shichuan River Basin using Gibbs diagram, Piper triangle diagram, correlation analysis, factor analysis, and main ion ratio method. The enhanced Nemerow comprehensive index method and fuzzy comprehensive evaluation method are employed for river water quality assessment. The findings reveal that runoff water has a weak alkaline nature with low salinity. The hydrochemical type of river water includes Ca2++Mg2++Na+-SO4 2-, Ca2++Mg2+-SO4 2-+Cl-+HCO3 -, Ca2++Na+-SO4 2-+Cl-+HCO3 -. Silicite and dolomite weathering are identified as primary influencing factors, while evaporite weathering also contributes to variations in chemical composition within the basin's waters. Ca2+, Mg2+, SO4 2- and HCO3 - originate from carbonate rock and silicate rock weathering processes, whereas Na+, K+ and Cl-, are primarily derived from evaporite weathering influenced by domestic sewage and agricultural activities. Agricultural production practices along with discharge of domestic sewage have an impact on Na+, K+, Cl- and NO3 -concentrations in aquatic systems. Water quality at all three monitoring sections falls under level IV classification. Phosphorus emerges as a key limiting factor for eutrophication within this basin's watersheds.

Slab melting boosts the mantle wedge contribution to Li-rich magmas

The lithium cycling in the supra-subduction mantle wedge is crucial for understanding the generation of Li-rich magmas that may potentially source ore deposition in continental arcs. Here, we look from the mantle source perspective at the geological processes controlling the Li mobility in convergent margins, by characterizing a set of sub-arc mantle xenoliths from the southern Andes (Coyhaique, western Patagonia). The mineral trace element signatures and oxygen fugacity estimates (FMQ > + 3) in some of these peridotite xenoliths record the interaction with arc magmas enriched in fluid-mobile elements originally scavenged by slab dehydration. This subduction-related metasomatism was poorly effective on enhancing the Li inventory of the sub-arc lithospheric mantle, underpinning the inefficiency of slab-derived fluids on mobilizing Li through the mantle wedge. However, major and trace element compositions of mantle minerals in other xenoliths also record transient thermal and chemical anomalies associated with the percolation of slab window-related magmas, which exhibit an “adakite”-type geochemical fingerprint inherited by slab-derived melts produced during ridge subduction and slab window opening event. As these melts percolated through the shallow (7.2–16.8 kbar) and hot (952–1054 °C) lithospheric mantle wedge, they promoted the crystallization of metasomatic clinopyroxene having exceptionally high Li abundances (6–15 ppm). Numerical modeling shows that low degrees (< 10%) of partial melting of this Li-rich and fertile sub-arc lithospheric mantle generates primitive melts having two-fold Li enrichment (~13 ppm) compared with average subduction-zone basalts. Prolonged fractional crystallization of these melts produces extremely Li-enriched silicic rocks, which may stoke the Li inventory of mineralizing fluids in the shallow crust.

Biogeochemical Aspects of Transformation of Humic Substances and Silicate Rocks during Freezing–Thawing

Biogeochemical Aspects of Transformation of Humic Substances and Silicate Rocks during Freezing–Thawing

Multi-method characterization of groundwater nitrate and sulfate contamination by karst mines in southwest China

Groundwater contamination by nitrate and sulfate in mining areas is a significant challenge. Consequently, the inputs sources of these contaminants and their evolution have received considerable attention, with the knowledge gained critical for improved management of water quality. This study integrated data on multiple stable isotopes and water chemistry data and a Bayesian isotope mixing model to investigate the relative contributions of inputs sources of sulfate and nitrate sources to bodies of water in a karst mining area in southwest China. The outcomes indicated that hydrochemical component in the water bodies of the study area is mainly derived from the dissolution of silicate rocks, carbonate rocks and sulfate minerals as well as the oxidation of sulfides. The human and agricultural wastewater, soil nitrogen, and fertilizers were the predominant inputs sources of nitrate to the mine water environment; the predominant inputs sources of sulfide were mineral oxidation, evaporite dissolution, atmospheric deposition, and sewage. Groundwater is mainly recharged from atmospheric precipitation, and surface water is closely hydraulically connected to groundwater. Nitrogen and oxygen isotope composition and water chemistry indicative of nitrification dominate the nitrogen cycle in the study area. The oxidation of pyrite and bacterial sulfate reduction (SRB) had no significant impact on the stable isotopes of groundwater. The results of this study demonstrate the inputs of different sources to nitrate and sulfate in karst mines and associated transformation processes. The results of this study can assist in the conservation of groundwater quality in mining areas and can act as a reference for future related studies.

What is the source of magnesium in hydrothermal dolomites? New insights from coupling δ26Mg - ∆47 isotopes

The occurrence of fault-controlled hydrothermal dolomitization (HTD) is ubiquitous across stratigraphic records and has been extensively studied due to its association with economic resources. The origin of HTD is often evaluated by combining carbonate geochemistry, fluid inclusion thermometry and reactive transport modelling. However, multiple diagenetic overprinting events can obscure original geochemical signatures. Here, we demonstrate the applicability of two combined isotope systems, magnesium and carbonate clumped isotopes (δ26Mg - ∆47), to trace the source of fluid and magnesium in basin-scale HTD from the Western Canadian Sedimentary Basin (WCSB) and Southern China. Extensive studies in these regions, providing tectono-stratigraphic information and dolomitization models, furnish a robust scenario to evaluate the new isotopic data. Our findings reveal that while the previous geochemical data (δ18Ofluid and 87Sr/86Sr) are partly compatible with dolomitization from seawater, the elevated δ26Mg and δ18Ofluid values (up to -0.3‰ and +11‰, respectively) and the high temperatures (up to 320 °C) are not consistent with dolomitization from seawater alone. Considering this, the uniform mean δ26Mg values of silicate rocks (-0.25‰) and the occurrence of basement-rooted faults in the study areas, the hypothesis from prior work that dolomitization was initially driven by seawater that progressively mixed with crustal fluids sourced from underlying basement rocks, was supported. As the δ26Mg values may reflect the isotopic signature of the fluid and the leached host rocks, when combined with ∆47-derived temperatures, it results in an effective tracer of fluid and Mg sources during dolomitization in tectonically complex basins that are otherwise challenging to unravel. A comparison of our results paints a global picture of isotopic imprints in hydrothermal dolomite and further demonstrate the ability of Mg isotopes to differentiate between dolomitization from seawater versus evaporated brines and also through Mg-rich crustal fluids.

Soil carbon management and enhanced rock weathering: The separate fates of organic and inorganic carbon

AbstractSoil carbon (C) management has been promoted as one of the few readily available strategies to mitigate the rising concentration of atmospheric CO2 and its associated impacts on climate change. One of these carbon management strategies is enhanced rock weathering (ERW) which involves adding crushed silicate rocks to the soil. These rocks weather and remove atmospheric CO2 by converting it into bicarbonate in solution. The approach requires careful interpretation of the differences between soil organic carbon (SOC) and soil inorganic carbon (SIC) and their measurement, with implications for land management and C credit accounting. In this Opinion, we emphasise the distinct nature and fates of SOC and SIC, advocating for their separate management, particularly in C credit schemes. It is imperative that protocols for soil C management explicitly recognise the difference between SOC and SIC to prevent any ambiguity. Farmers should be able to claim credits for increases in SOC alongside and independently of any claim for credits for ERW (i.e. SIC). Despite the potential of ERW for C removal, we emphasise that further research is needed to improve the measurement and monitoring of SIC and to understand ERW's potential implications for SOC turnover and greenhouse gas emissions.Highlights Enhanced Rock Weathering increases dissolved inorganic carbon (bicarbonate). Soil organic carbon (SOC) may be influenced by Enhanced Rock Weathering. Carbon credit via Enhanced Rock Weathering is separate from credit linked to soil organic carbon. Soil organic matter and enhanced rock weathering both have roles to play for carbon credits.