Search Results (201)

Rizhao Reservoir, Shandong Province, China, as a key regional water supply hub, provides water for domestic, industrial, and agricultural uses in and around Rizhao City by intercepting runoff, which plays a central role in guaranteeing water supply security and supporting regional development. This study systematically collected 66 surface water samples to elucidate the hydrochemical characteristics within the reservoir area, identify the principal influencing factors, and clarify the sources of dissolved ions, aiming to enhance the understanding of the prevailing water quality conditions. A systematic analysis of hydrochemical facies, solute provenance, and governing processes in the study area’s surface water was conducted, employing an integrated mathematical and statistical approach, comprising Piper trilinear diagrams, correlation analysis, and ionic ratios. Meanwhile, the entropy weight-based water quality index (EWQI) and irrigation water quality evaluation methods were employed to assess the surface water quality in the study area quantitatively. Analytical results demonstrate that the surface water system within the study area is classified as freshwater with circumneutral to slightly alkaline properties, predominantly characterized by Ca-HCO₃ and Ca-Mg-SO₄-Cl hydrochemical facies. The evolution of solute composition is principally governed by rock–water interactions, whereas anthropogenic influences and cation exchange processes exert comparatively minor control. Dissolved ions mostly originate from silicate rock weathering, carbonate rock dissolution, and sulfate mineral dissolution processes. Potability assessment via the entropy-weighted water quality index (EWQI) classifies surface waters in the study area as Grade I (Excellent), indicating compliance with drinking water criteria under defined boundary conditions. Irrigation suitability analysis confirms minimal secondary soil salinization risk during controlled agricultural application, with all samples meeting standards for direct irrigation use. Full article

The southeastern Hainan Island boasts abundant hydrothermal resources, most of which are exposed as thermal springs. Analyzing the hydrochemical characteristics, hydrochemical evolutionary mechanisms, and material transition of these resources is significant for their exploitation and utilization. This study investigated the Nanping geothermal field in southeastern Hainan Island, using five groups of geothermal water samples collected in 2022, as well as seven groups of geothermal water samples, one group of shallow groundwater samples, and one group of surface water samples taken in 2023. Specifically, this study examined water–rock interactions in the geothermal field using the Gibbs model, ion ratios, chloro-alkaline indices (CAIs), and the sodium adsorption ratio (SAR). Moreover, the mineral transfer process in groundwater was analyzed using inverse hydrogeochemical simulation. The results indicate that in the study area the geothermal water temperatures range from 64 °C to 80 °C, pH values from 8.32 to 8.64, and TDS concentrations from 431 mg/L to 623 mg/L. The primary hydrochemical types of geothermal water in the study area include Cl-Na and Cl·HCO₃-Na, suggesting low-temperature, slightly alkaline geothermal water. The hydrochemical components of geothermal water in the study area are primarily affected by water–rock interactions. Besides the dissolution of silicate minerals and halite, cation exchange reactions contribute greatly to the formation of Na⁺ and K⁺ in geothermal water. Geothermal water receives recharge from the atmospheric precipitation of the Diaoluo Shan area in the northwest of the study area, with the recharge elevation ranging from 967 to 1115 m. The inverse hydrogeochemical simulation results reveal that during the water–rock interactions, silicate minerals, clay minerals, gypsum, and halite dissolve, while quartz and carbonate minerals precipitate. Additionally, these processes are accompanied by cation exchange reactions dominated by the replacement of Na⁺ in surrounding rocks by Ca²⁺ in geothermal water. This study can provide a geological basis for the exploitation, utilization, and management of the Nanping geothermal field. Full article

The Qieliekeqi siderite deposit, located in the Tashkurgan block of western Kunlun, is a carbonate-hosted iron deposit with hydrothermal sedimentary features. This study integrates whole-rock geochemistry, stable isotopes, and zircon U–Pb–Hf data to investigate its metallogenic evolution. Coarse-grained siderite samples, formed in deeper water, exhibit average Al₂O₃/TiO₂ ratios of 29.14, δEu of 2.69, and δCe of 0.83, indicating hydrothermal fluid dominance with limited seawater mixing. Banded samples from shallower settings show an average Al₂O₃/TiO₂ of 17.07, δEu of 3.18, and δCe of 0.94, suggesting stronger seawater interaction under oxidizing conditions. Both types are enriched in Mn, Co, and Ba, with low Ti and Al contents. Stable isotope results (δ¹³C_PDB = −6.0‰ to −4.6‰; δ¹⁸O_SMOW = 16.0‰ to 16.9‰) point to seawater-dominated fluids with minor magmatic and meteoric contributions, formed under open-system conditions at avg. temperatures of 53 to 58 °C. Zircon U–Pb dating yields an age of 211.01 ± 0.82 Ma, with an average εHf(t) of −3.94, indicating derivation from the partially melted ancient crust. These results support a two-stage model involving Late Cambrian hydrothermal sedimentation and Late Triassic magmatic overprinting. Full article

This study systematically unravels the hydrochemical evolution mechanisms and driving forces in multi-aquifer systems of Qingdao, a coastal economic hub. Integrated hydrochemical analysis of porous, fissured, and karst water, combined with PHREEQC modeling and Positive Matrix Factorization (PMF), deciphers water–rock interactions and anthropogenic perturbations. Groundwater exhibits weak alkalinity (pH 7.2–8.4), with porous aquifers showing markedly higher TDS (161.1–8203.5 mg/L) than fissured (147.7–1224.8 mg/L) and karst systems (361.1–4551.5 mg/L). Spatial heterogeneity reveals progressive hydrochemical transitions (HCO₃-Ca → SO₄-Ca·Mg → Cl-Na) in porous aquifers across the Dagu River Basin. While carbonate (calcite) and silicate weathering govern natural hydrochemistry, evaporite dissolution and seawater intrusion drive severe groundwater salinization in the western Pingdu City and the Dagu River Estuary (localized TDS up to 8203.5 mg/L). PMF source apportionment identifies acid deposition-enhanced dissolution of carbonate/silicate minerals, with nitrate contamination predominantly sourced from agricultural runoff and domestic sewage. Landfill leachate exerts pronounced impacts in Laixi and adjacent regions. This study offering actionable strategies for salinity mitigation and contaminant source regulation, thereby providing a scientific framework for sustainable groundwater management in rapidly urbanizing coastal zones. Full article

Groundwater nitrate (NO₃⁻) contamination has emerged as a critical global environmental issue, posing serious human health risks. This study systematically investigated the hydrochemical processes, sources of NO₃⁻ pollution, the impact of land use on NO₃⁻ pollution, and drinking water safety in an urban area of southwestern China. Thirty-one groundwater samples were collected and analyzed for major hydrochemical parameters and dual isotopic composition of NO₃⁻ (δ¹⁵N-NO₃⁻ and δ¹⁸O-NO₃⁻). The groundwater samples were characterized by neutral to slightly alkaline nature, and were dominated by the Ca-HCO₃ type. Hydrochemical analysis revealed that water–rock interactions, including carbonate dissolution, silicate weathering, and cation exchange, were the primary natural processes controlling hydrochemistry. Additionally, anthropogenic influences have significantly altered NO₃⁻ concentration. A total of 19.35% of the samples exceeded the Chinese guideline limit of 20 mg/L for NO₃⁻. Isotopic evidence suggested that primary sources of NO₃⁻ in groundwater include NH₄⁺-based fertilizer, soil organic nitrogen, sewage, and manure. Spatial distribution maps indicated that the spatial distribution of NO₃⁻ concentration correlated strongly with land use types. Elevated NO₃⁻ levels were observed in areas dominated by agriculture and artificial surfaces, while lower concentrations were associated with grass-covered ridge areas. The unabsorbed NH₄⁺ from nitrogen fertilizer entered groundwater along with precipitation and irrigation water infiltration. The direct discharge of domestic sewage and improper disposal of livestock manure contributed substantially to NO₃⁻ pollution. The nitrogen fixation capacity of the grassland ecosystem led to a relatively low NO₃⁻ concentration in the ridge region. Despite elevated NO₃⁻ and F⁻ concentrations, the entropy weighted water quality index (EWQI) indicated that all groundwater samples were suitable for drinking. This study provides valuable insights into NO₃⁻ source identification and hydrochemical processes across varying land-use types. Full article

With the intensification of human activities, the water resource environment in the karst mountainous area of central Shandong has undergone significant changes, directly manifested in the cessation of karst spring flows and the occurrence of karst collapses within the spring basin in the Laiwu Basin. To support the scientific development and management of karst water, this study utilizes comprehensive analysis and deuterium-oxygen isotope test data from surveys and sampling of 20 typical karst springs conducted between 2016 and 2018. By integrating mathematical statistics, correlation analysis, and ion component ratio methods, the study analyzes the genesis, hydrochemical ion component sources, and controlling factors of typical karst springs in the Laiwu Basin. The results indicate that the genesis of karst springs in the Laiwu Basin is controlled by three factors: faults, rock masses, and lithology, and can be classified into four types: water resistance controlled by lithology, by faults, by basement, and by rock mass. The karst springs are generally weakly alkaline freshwater, with the main ion components being HCO₃⁻ and Ca²⁺, accounting for approximately 55.02% and 71.52% of the anion and cation components, respectively; about 50% of the sampling points have a hydrochemical type of HCO₃·SO₄-Ca·Mg. Stable isotope (δ¹⁸O and δD) results show that atmospheric precipitation is the primary recharge source for karst springs in the Laiwu Basin. There are varying degrees of evaporative fractionation and water–rock interaction during the groundwater flow process, resulting in significantly higher deuterium excess (d-excess) in the sampling points on the southern side of the basin compared to the northern side, indicating clear differentiation. The hydrochemical composition of the karst groundwater system is predominantly governed by water–rock interactions during flow processes and anthropogenic influences. Carbonate dissolution (primarily calcite) serves as the principal source of HCO₃⁻, SO₄²⁻, Ca²⁺, and Mg²⁺, while evaporite dissolution and reverse cation exchange contribute to the slight enrichment of Ca²⁺ and Mg²⁺ alongside depletion of Na⁺ and K⁺ in spring waters. Saturation indices (SI) reveal that spring waters are saturated with respect to gypsum, aragonite, calcite, and dolomite, but undersaturated for halite. The mixing of urban domestic sewage, agricultural planting activities, and the use of manure also contributes to the formation of Cl⁻ and NO₃⁻ ions in karst springs. Full article

The paper reports the first findings of a series of alkali carbonate, chloride, and sulfate minerals among the usual groundmass kimberlite minerals, such as olivine, phlogopite, monticellite, calcite, spinel-group minerals, perovskite, ilmenite, rutile, and apatite. The sample was collected from an unserpentinized coherent kimberlite dyke that crosscuts earlier volcaniclastic kimberlite in the central part of the Udachnaya-East pipe. This rock can be described as primary/original kimberlite that did not interact with external/internal hydrothermal fluids either during its formation or after its crystallization. At least three alkali-rich carbonates have been found, a previously unknown (and perhaps, a new one) Na-, Ca-, K-, and S-rich carbonate with the calculated empirical formula (Na,K)₆Ca₄(CO₃,SO₄)₇, shortite Na₂Ca₂(CO₃)₃, and nyerereite (Na,K)₂Ca(CO₃)₂. Chlorides in this kimberlite are halite NaCl and sylvite KCl, and the sulfate is aphthitalite K₃Na(SO₄)₂. The content of the Na-Ca-K-S-rich carbonate in the rock is ~15 vol %, that of shortite and halite is ≤5 vol % each, and those of sylvite and aphthitalite are ≤1 vol %. All alkali-rich minerals are of late magmatic origin. This follows from that (i) the studied kimberlite does not contain any secondary water-rich minerals of hydrothermal transformation of the rocks, such as serpentine, chlorite or iowaite; and (ii) crystalline inclusions of such usual kimberlite minerals as olivine, phlogopite, monticellite, calcite, spinel, perovskite, and apatite were found within Na-Ca-K-S-rich carbonate and halite. This publication expands the list of minerals of magmatic origin identified in the groundmass of worldwide kimberlites by at least three minerals: Na-Ca-K-S-rich (new?) carbonate, sylvite, and aphthitalite. It is important to note that all alkali carbonates, chlorides, and sulfates are unstable during secondary hydrothermal alterations of kimberlites, and hence, these minerals cannot be found in serpentinized rocks. Full article

CO₂ sequestration in coal is effective for reducing carbon emissions, but related projects have encountered challenges in sustained CO₂ injection, highlighting the need for a comprehensive understanding of CO₂ sequestration in coal. This study reviews variations in the properties of coal/rock during/after CO₂ injection, demonstrating the potential and stability of CO₂ sequestration in coal. The coal with a high V_L-CO₂/V_L-CH₄ is accompanied by high CO₂ sequestration capacity. The matrix swelling and acid corrosion restrict CO₂ sequestration efficiency, which can be enhanced by employing coatings and increasing permeability. Long-term CO₂–water–rock interactions weaken the integrity of coal/caprocks and decrease the adsorption capacity of coal, leading to the CO₂ leakage risk. Three issues are critical in future studies: (1) Increasing CO₂ adsorption capacity. (2) Establishing optimal approaches to enhance CO₂ injection efficiency. (3) Accurately predicting variations in the adsorption capacity of deep coal and the integrity of coal/caprocks during long-term CO₂–water–rock interactions. This review provides foundations for formulating CO₂ sequestration strategies in coal. Full article

Carbonate rock slopes in reservoir environments are increasingly exposed to dissolution-induced deterioration due to water level fluctuations. However, the influence of internal structures—particularly calcite veins—on dissolution behavior remains inadequately understood. The acid-induced dissolution of limestone by a sulfuric acid solution leads to the removal of soluble minerals and changes to the rock structure. Natural variation in rock structures—particularly in the presence, density, and morphology of calcite veins—can significantly affect the dissolution process and its outcomes. In this study, we obtained three types of Triassic limestone from the same host rock but with varying vein structures from the Three Gorges Reservoir area. Cylindrical rock specimens were prepared to investigate the acid-induced dissolution behavior of limestone in a sulfuric acid solution. We identified and analyzed the macrostructures on the rock specimens before and after the interaction. Additionally, SEM was employed to observe the microstructures of the specimens before and after the acid-induced dissolution, and fractal dimension analysis was conducted on the SEM images to quantify surface complexity. Furthermore, we used a focused ion beam–scanning electron microscope (FIB-SEM) with an automatic mineral identification and characterization system, as well as mineral roundness calculation, for mineral identification and analysis. Based on the experiments and analyses, we determined the following: The contact surfaces between the host rock and the calcite veins increase the dissolution areas between the limestone and the sulfuric acid solution, intensifying the dissolution reactions, enhancing the connectivity of the original microstructural planes, and generating new, highly extended dissolution fissures. The calcite veins facilitate the entry of sulfuric acid solution into the limestone, intensifying the dissolution of the edges and corners of dolomite and resulting in the gradual rounding of dolomite shapes. Quantitatively, the limestone with dense, fine calcite veins exhibited the most severe dissolution, with water absorption rates nearly twice as high as the non-veined samples (0.13% vs. 0.07%), a 2.2% reduction in fractal dimension, and a 19.53% increase in dolomite roundness with the 1 ≤ R ≤ 3 interval, indicating significantly enhanced surface complexity and mineral reshaping. In summary, the presence of more calcite veins, regardless of their width, leads to more severe rock dissolution. Full article

Taking the coastal area of Binhai County, Jiangsu Province, as an example, this study first investigated the basic natural geography and the regional geological and hydrogeological conditions of the study area, and then carried out in-depth geophysical prospecting, hydrogeological tests, geothermal temperature monitoring, hydrochemistry and isotope analyses, and other studies based on the results to comprehensively and systematically reveal the genesis mechanism of the geothermal water resources of this coastal area from multiple perspectives. The results showed the following: the geothermal water in this area mainly comes from atmospheric precipitation; the deep east–northwest interlaced fracture is the recharge and transportation channel; the Cambrian–Ordovician carbonate rock layer, enriched by the development of cavernous fissures, forms the thermal storage layer; the underground heat mainly comes from the upward heat flow along the deep fracture and the natural warming of the strata; and the thermal reservoir cover comprises Paleozoic and Mesozoic clastic rocks that have a high mud content and form a thick layer. The genesis mode of this area is as follows: the atmospheric precipitation infiltrates and is recharged through the exposed alpine carbonate fissures in the Lianyungang area, and then it is transported to the south along the large deep fracture under the action of a high hydraulic pressure head; meanwhile, it is heated by the heat flow in the deep part of the fracture and water–rock interactions with the strata occur. Geothermal water with a calculated thermal storage temperature of 83.6 °C is formed at a depth of 2.9 km, which is blocked by the intersection of the northeast and northwest fractures to form a stagnant zone in the coastal area. Full article

The Aït Abdellah copper deposit in the Bou Azzer-El Graara inlier of the Moroccan Anti-Atlas provides key insights into structurally and lithologically controlled mineralization in Precambrian terranes. The deposit is hosted in feldspathic sandstones of the Tiddiline Group, which unconformably overlie the Bou Azzer ophiolite, and is spatially associated with a NE–SW-trending shear zone. This zone is characterized by mylonitic fabrics, calcite veining, and an extensive network of fractures, reflecting a two-stage deformation history involving early ductile shearing followed by brittle faulting and brecciation. These structural features enhanced rock permeability, enabling fluid flow and metal precipitation. Copper mineralization includes primary sulfides such as chalcopyrite, bornite, pyrite, chalcocite, digenite, and covellite, as well as supergene minerals like malachite, azurite, and chrysocolla. Sulfur isotope values (δ³⁴S = +5.9% to +22.8%) indicate a mixed sulfur source, likely derived from both ophiolitic rocks and volcano-sedimentary sequences. Carbon and oxygen isotope data suggest fluid interaction with marine carbonates and meteoric waters, potentially linked to post-Snowball Earth deglaciation processes. Fluid inclusion studies reveal homogenization temperatures ranging from 195 °C to 310 °C and salinities between 5.7 and 23.2 wt.% NaCl equivalent, supporting a model of fluid mixing between magmatic-hydrothermal and volcano-sedimentary sources. The paragenetic evolution of the deposit comprises three stages: (1) early hydrothermal precipitation of quartz, dolomite, sericite, pyrite, and early chalcopyrite and bornite; (2) a main mineralizing stage characterized by fracturing and deposition of bornite, chalcopyrite, and Ag-bearing sulfosalts; and (3) a late supergene phase with oxidation and secondary enrichment. The Aït Abdellah deposit is best classified as a shear zone-hosted copper system with a complex, multistage mineralization history. The integrated analysis of structural features, mineral assemblages, isotopic signatures, and fluid inclusion data reveals a dynamic interplay between deformation processes, hydrothermal alteration, and evolving fluid sources. Full article

The Axi gold deposit, which is located in the Tulasu Basin of the West Tianshan orogenic belt in Northwest China, features vein-type ore bodies hosted in radial structural fractures formed due to volcanic activity. The deposit experienced three distinct mineralization stages: Stage I, characterized by the microcrystalline quartz–pyrite crust; Stage II, characterized by quartz–sulfide–native gold veins; and Stage III, characterized by quartz–carbonate veins. Fluid inclusion studies have identified four types of inclusions: pure vapor, vapor-rich, liquid-rich, and pure liquid. The number of vapor-rich inclusions decreases when moving from Stage I to Stage III, whereas the number of liquid-rich inclusions increases. The fluid temperature gradually decreases from 178–225 °C in Stage I to 151–193 °C in Stage II and further to 123–161 °C in Stage III, whereas the fluid salinity decreases slightly from 2.1%–5.1% wt.% NaCl eqv to 1.4%–4.6% wt.% NaCl eqv and finally to 0.5%–3.7% wt.% NaCl eqv. As suggested by the results of the oxygen, hydrogen, and carbon isotope analyses, the ore-forming fluids were primarily meteoric water. Sulfur isotopic compositions indicate a single deep mantle source. The lead isotopic compositions closely resemble those of Dahalajunshan Formation volcanic rocks, indicating that these rocks were the primary source of the ore-forming material. In addition, gold mineralization formed in a Devonian–Early Carboniferous volcanic arc environment. Element enrichment was mainly caused by the circulation of heated meteoric water through the volcanic strata, while fluid boiling and water–rock interactions were the main mechanisms driving element precipitation. The integrated model developed in this study underscores the intricate interplay between volcanic processes and meteoric fluids during the formation of the Axi gold deposit, offering a robust framework for an understanding of the formation processes and enhancing the predictive exploration models in analogous geological settings. Full article

Hydrogeochemical characteristics and temperature variations in fault-controlled, deep-circulation thermal springs elucidate water–rock interaction dynamics and hydrothermal circulation depths, providing critical insights into fault permeability and stress accumulation. To investigate the coexistence of high-temperature and medium-low-temperature thermal springs on small-scale faults and their distinct circulation mechanisms, hydrochemical and isotopic analyses were conducted on 13 water samples (9 proximal on the Xiangbaihe Fault) in western Yunnan. The hot springs along the Xiangbaihe Fault are predominantly classified as the Na-HCO₃ type, derived from carbonate and aluminosilicate hydrolysis. δ²H and δ¹⁸O confirmed a meteoric origin, with recharge elevations spanning 2465–3286 m (Gaoligong Mountain). Inverse hydrochemical modeling demonstrated progressive mineral transfer and water–rock interactions along the fault’s east–west axis. Conservative elements (Cl, Li) suggested a shared geothermal fluid source or reservoir affiliation. BLZ reservoir temperatures (194–221 °C) were classified as a high-temperature system, whereas others (58–150 °C) represented medium-low-temperature systems. Although each thermal spring represents a distinct geothermal system, reservoir interconnectivity is inferred. Notably, despite uniform lithology, variations in spring temperature and elemental composition are attributed to a subsurface magma chamber beneath BLZ, heterogeneous fault geometries, differential reservoir temperatures, and variable cold-water mixing ratios. This study establishes a framework for understanding groundwater circulation in small-scale fault-associated geothermal systems, with implications for tectonic activity monitoring and geothermal resource assessment. Full article

A thorough understanding of the chemistry involved in reinjecting heat-depleted geothermal water into poorly consolidated sandstone is vital for the effective design of treatments targeting subsurface rock formations. The intricate chemical interactions occurring within sandstone systems can result in the dissolution of certain minerals and the subsequent precipitation of others, which may significantly contribute to damage within the formation. This process can alter the physical properties of the rock, potentially leading to reduced permeability and other challenges in resource extraction. Thus, it is imperative to monitor not only the concentration of various chemical species present in the geothermal water and sandstone, but also the spatial distribution of these geochemical reactions. By doing so, we can better predict and mitigate their potential adverse effects on rock formations, ensuring the long-term success and efficiency of geothermal energy extraction and other subsurface activities. In this study, we conducted laboratory experiments using both model and natural formation waters, as well as rock samples, to investigate water–rock interactions in a sandstone reservoir in the Szentes area of Hungary. Geochemical models were run with two different thermodynamic databases to simulate laboratory experiments, predict the effects of heat-depleted geothermal water reinjection into the reservoir, and assess predictions of different geochemical databases. Our study shows that calcite dissolves while quartz, kaolinite, and dolomite form. Other mineral reactions, however, remain less certain. The PHREEQC database indicates chlorite dissolution along with the formation of small amounts of feldspars and hematite, whereas the Thermoddem database predicts montmorillonite dissolution and chlorite precipitation. The reservoir porosity and permeability are expected to change over time as a result of mineral reactions. Modeling results, however, indicate negligible porosity changes as the reservoir reaches equilibrium state. The general concept proposed here, which focuses on the geochemical properties of the reinjected water and reservoir, provides a framework for detailed analysis of the geothermal system—a critical step for ensuring sustainable geothermal operations. Full article

Calcite in hydrocarbon reservoirs records abundant information about diagenetic fluids and environments. Understanding the formation mechanisms of calcite is crucial for predicting reservoir characteristics and hydrocarbon migration. This study identifies the types of authigenic calcite present in the Lower Paleozoic carbonate reservoirs of the Bohai Bay Basin through petrographic analysis, cathodoluminescence, and other experimental methods. By integrating electron probe microanalysis, in situ isotopic analysis, and fluid inclusion studies, we further constrain the source of the diagenetic fluids responsible for the authigenic calcite. The results show that there are at least three types of authigenic calcite in the Lower Paleozoic carbonate reservoirs of the Bohai Sea. Calcite cemented in the syn-depositional-to-early-diagenetic stage displays very weak cathodoluminescence, with δ¹³C and δ¹⁸O and paleo-salinity distributions similar to those of micritic calcite. These features suggest that the calcite was formed during burial heating by sedimentary fluids. Calcite filling fractures shows heterogeneous cathodoluminescence intensity, ranging from weak to strong, indicating multiple stages of cementation. The broad elemental variation and multiple cementation events suggest that the diagenetic fluid sources were diverse. Isotopic data show that samples with carbon isotope values greater than −2.9‰ likely formed through water–rock interaction with fluids retained within the strata, whereas samples exhibiting more negative δ¹³C were formed from a mixed-source supply of strata and mantle-derived fluids. Calcite that fills karst collapse pores exhibits alternating bright and dark cathodoluminescence, strong negative δ¹⁸O shifts, and variability in trace elements such as Mn, Fe, and Co. These characteristics indicate a mixed origin of diagenetic fluids derived from both meteoric freshwater and carbonate-dissolving fluids. Full article