Silicic Research Articles

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.

Formation of silicic crust on early Earth and young planetary bodies in an Iceland-like setting

Four billion years ago, Earth’s surface was covered with a thick basaltic crust and, similar to other rocky planets and the Moon, parts of this basaltic crust underwent partial melting to produce silicic crust. On Earth, silicic crust grew into the continents. An analogue of a pre-subduction early Earth and rocky planetary bodies is found in Iceland, where poorly understood granitic rocks are encased in thick basaltic crust away from any active subduction zone. Here, we investigate these Icelandic granitoids to understand the mechanisms that generated the Earth’s oldest continents, and silicic rocks on Mars and Venus. New geochemical data from silicic Icelandic intrusions, show that the granitoids are formed through partial melting of the Icelandic crust, but are compositionally unlike early Earth continental material. We show that intra-crustal partial melting of basalt can potentially form silicic material on other planetary bodies but cannot produce the first continents on Earth.

Nanoscale characterization of Ediacaran microfossils from lower Doushantuo formation chert nodules

Microfossils identification, especially in very old rocks, is extremely challenging because morphological and chemical signatures of microfossils are subtle and inevitably altered with aging. Chert nodules from the Doushantuo Formation in the Yangtze Gorges area of South China have captured significant interest due to their remarkable preservation of Ediacaran microfossils. To understand the taphonomic processes leading to an exceptional preservation of microbes in these rocks, we studied the morphological and chemical features of microfossils within the lower Doushantuo Formation chert nodules down to atomic scales via advanced microscopy techniques. Our results align with previous studies, confirming that most microfossils there are preserved by silicification. Further analysis of a representative filamentous microfossil, Polytrichoides lineatus, reveals that both the cell wall (or extracellular sheath) and cytoplasm are preserved by loose aggregates of subrounded or irregular quartz grains, along with patchy organic residuals, which are distinctive from the closely packed and angular-shaped quartz grains in the non-fossil matrix of the chert nodule. The cell wall or extracellular sheath likely provided narrower spaces and more nucleation sites for silicification, resulting in smaller quartz grains (i.e., 115 ± 42 nm) compared to those formed in the cytoplasm (i.e., 1150 ± 258 nm). The permeation and precipitation of quartz grains within the cell wall or extracellular sheath could contribute to an exceptional preservation of subcellular structures. This study offers valuable insights into the preservation of microbes in the Doushantuo Formation chert nodules and even older siliceous sedimentary rocks.

Cobalt and nickel distribution and controlling factors in the Bushveld layered complex

The Bushveld Complex is the largest known layered intrusion in the world and has been extensively studied. However, there remains an absence of systematic investigations of cobalt (Co) and nickel (Ni) distribution at various scales. Elements Co and Ni behave varying degrees of compatibility within chromite, silicates, and sulfides, making them effective proxies for elucidating chemical competition and interaction among these minerals. This study aims to characterize Co and Ni distribution in olivine, pyroxenes, chromite, and whole rocks from different seams of the Bushveld Complex and to reveal their controlling factors. Our results indicate large variations of whole-rock Co and Ni concentrations, with a decreasing sequence of dunites (Co: 156–222 ppm; Ni: 2208–2750 ppm) > harzburgites (Co: 87.8–174 ppm; Ni: 152–2050 ppm) > pyroxenites (Co: 58.7–143 ppm; Ni: 387–1947 ppm) > norites (Co: 16.0–113 ppm; Ni: 153–646 ppm) > anorthosites (Co: 3.20–16.3 ppm; Ni: 19.7–97.2 ppm). In general, olivine has higher Ni contents (717–4496 ppm) and lower Co (105–239 ppm) than chromite (Ni: 524–1948 ppm; Co: 236–563 ppm). Pyroxenes have apparently low Co (orthopyroxene: 39.7–184 ppm; clinopyroxene: 17.2–114 ppm) and Ni contents (orthopyroxene: 224–1195 ppm; clinopyroxene: 177–831 ppm). Chromite in chromitites has lower Co content than that in other rocks. The whole-rock and mineral Co and Ni variations in the stratigraphic profile are closely related with lithology, mineral assemblages and element partition coefficients in minerals. The Co contents in the chromite and pyroxenes vary alternately with the chromitites and rock seams, with lower Co contents in ore samples than that in silicate rocks. Whole rocks and mineral separates in the Merensky Reef exhibit the highest Ni contents (whole-rock: up to 4000 ppm; orthopyroxene: 1035–1195 ppm; clinopyroxene: 730–831 ppm; chromite: 1760–1948 ppm), which are likely attributed to sulfide segregation and diffusion between sulfides and other minerals. In addition, the sulfide segregation may also be a main factor resulting in Co-Ni decoupling in pyroxenes from the Main Zone of the Bushveld Complex.

Novel approach evaluating powdered raw and hydrothermally treated syenite as stonemeal for tropical environments: Potential effects on groundwater quality and agricultural suitability

Soluble fertilizers, particularly potash, are often prohibitively expensive or unavailable in Africa. Consequently, alternatives such as powdered silicate rocks, both raw and hydrothermally treated, are being explored as potential solutions, especially for acidic tropical soils. This study investigates the possible impacts of these rocks (syenite) on groundwater quality, which is a critical factor for agricultural activities. The powdered raw material underwent chemical and mineralogical characterization, including X-ray fluorescence and X-ray diffraction, followed by quantitative evaluation of materials by scanning electron microscopy. Both raw and 46 hydrothermally treated materials were subjected to sequential leaching cycles (1, 24, and 192 h) using deionized water, and the resulting leachates were analyzed by inductively coupled plasma atomic emission spectroscopy. Parameters such as electrical conductivity, total dissolved solids, soluble sodium percentage, sodium adsorption ratio, magnesium hazard, Kelly's ratio, and permeability index were also evaluated. Results from the 47 leachates indicated that 64 % of the samples exhibited excellent to acceptable water quality for irrigation purposes across all parameters. Conversely, 6 % to 13 % fell into the doubtful category, and 2 % to 24 % were classified as unsuitable. Consistency index and ratios of approximately 0.07 and 0.042, respectively, were determined using multi-criteria decision analysis (analytic hierarchy process: AHP), confirming the coherence of the decision and pairwise comparison matrix. The weighted coefficients for each criterion ranged from 0.06 to 0.2. Consequently, the optimal sample (Treatment 23) was identified, showing a hydrothermal temperature of 176 °C, a time of 3.9 h, a normality of 4.62, and a liquid-solid ratio of 0.24. This treatment met all high-water quality standards, including low salinity and sodium hazard, as corroborated by the US salinity laboratory and Wilcox diagrams. Furthermore, due to their nutrient release, low concentration of toxic elements, and effective buffering capacity (pH ∼ 10.6), these powdered syenites are suitable for application in acidic soils.

Hydrochemical Characteristics, Controlling Factors and Water Quality Evaluation of Groundwater Quality in Kono, Sierra Leone

Groundwater is a major source of drinking water and is considered an imperative component of the accessible water assets across Sierra Leone and many parts of the world. The degradation of groundwater can jeopardize drinking water availability and human health. 29 groundwater monitoring samples with 16 water quality parameters were analyzed. Descriptive statistics, Piper plots, Arc GIS spatial interpolation, Gibbs plots, ion ratio analysis, Wilcox diagram, water quality index (WQI), and entropy-weighted water quality index (EWQI) were used to investigate the hydrochemical characteristics, controlling factors and evaluate the groundwater quality in the study area. The results revealed that the groundwater mean concentration of NO3− in the mining concession was 34.00 mg/L which was above the permissible limit, Ca2+ and HCO3− are higher in the Koidu community compared to the mining concession water, indicating weakly alkaline with dominant anions and cations of HCO3− and Na+ + K+ respectively, and the hydrochemical types were mainly HCO3−·Ca2+ and HCO3− ·Na+. The order of anion concentration in groundwater was HCO3− &gt; NO3− &gt; SO42− &gt; Cl− and HCO3− &gt; SO42− &gt; NO3− &gt; Cl− in the mining concession and the Koidu community respectively. Cations were Ca2+ &gt; Na+, K+ &gt; Mg2+ &gt; Fe²⁺, and Ca2+ &gt; Na+ &gt; Mg2+ &gt; K+ &gt; Fe²⁺ in the mining concession and the Koidu community respectively. The interpretation of WQI and EWQI analysis exhibits 55.17% excellent, 17.24% good, 20.69% medium, 6.90% very poor, and 27.59% excellent, 24.14% good, 34.48% medium, 3.45% poor, and 10.34% very poor water respectively. Most of the sampling sites display similar trends to the WQI and EWQI. The solute source of groundwater was mainly controlled by water-rock interaction, cation exchange and the weathering of silicate and carbonate rocks were jointly the main contributors to the formation of the chemical components of groundwater in the study area, among which the main controlling factors of the groundwater were leaching, precipitate concentration and anthropogenic activities, and sulfate rock and carbonate rock dissolution. The overall water quality in the study area was suitable for human consumption but was polluted to an insignificant extent by mining activities. This study provides theoretical support and a decision-making basis for developing, utilizing, and protecting water resources in the study area.

Detrital Tourmalines in the Cretaceous–Eocene Julian and Brkini Flysch Basins (SE Alps, Italy and Slovenia)

In the SE Alps, two Cretaceous–Eocene flysch basins, Julian and Brkini, filled with turbidite sediments, are present. This study novelly reports heavy mineral assemblage counts and detrital tourmaline characterization for 11 samples. It is possible to define three different groups, characterized by the presence of (1) a clinopyroxene–epidote–low-ZTR (zircon+tourmaline+rutile; 5%) sample association, (2) a high-ZTR (&gt;48%)–garnet–apatite association and (3) a low-ZTR (&lt;40%)–Cr-spinel–garnet association. Detrital tourmalines from both the Julian and Brkini flysch basins are rather similar in composition, associated with metapelites and metapsammites coexisting or not coexisting with an Al-saturating phase, ferric-iron-rich quartz–tourmaline rocks and calc–silicate rocks; however, their number is drastically different. In fact, even if the percentage of heavy minerals is very low and similar in both basins (0.17–1.34% in weight), in the Julian basin, the number of tourmaline crystals is much lower than that in Brkini (1–14 vs. 30–100), suggesting an important change in the provenance area. Interestingly, the presence of a high amount of tourmaline derived from ferric-iron-rich quartz–tourmaline rocks and calc–silicate rocks makes these two basins different from all the Cretaceous flysch basins of Bosnia and the Northern Dinaric zone, where these supplies are missing or very limited.