Search Results (5)

This study characterized groundwater resources for the Nakivale sub-catchment of the transboundary Victoria Basin in Uganda using classical hydrochemical and stable isotopic approaches. Groundwater in the study area is essential for domestic, agricultural, and industrial uses. As a sub-domain of the larger Victoria Basin, it also plays a crucial role in shaping the hydrological characteristics of this vital transboundary basin, both in terms of quality and quantity fronts. This makes its sustainable management and development vital. The predominant groundwater type is Ca-SO₄, with other types including Ca-HCO₃, Na-Cl, Na-HCO₃, and Ca-Mg-SO₄-Cl. Hydrochemical facies analysis highlights the importance of rock–water interactions in controlling groundwater chemistry, mainly through incongruent chemical weathering of Ca-rich plagioclase feldspars and the oxidation of sulfide minerals, such as pyrite, which are prevalent in the study area. Groundwater recharge is primarily influenced by the area’s topography, with recharge zones characterized by lineament networks, located in elevated areas. Stable isotope analyses indicate that groundwater mainly originates from local precipitation, while tritium data suggest the presence of both recent and older groundwater (likely over 20 years old). The study’s comprehensive approach and findings contribute significantly to the understanding of groundwater systems in the region, thus providing valuable insights for policymakers and stakeholders involved in water resource management and development strategies. Full article

Chemical and physical denudation rates have been assessed in areas with different lithologies. Surprisingly, there are no studies that attempt to document these rates in the Poços de Caldas Alkaline Massif (PC), the largest alkaline magmatism in South America and an important Al supergene deposit in Brazil. Therefore, the chemical and physical denudation rates were assessed and explained in the PC. Surface water and rainwater samples were collected at the Amoras Stream basin, covering one complete hydrological cycle (2016). All samples were analyzed for dissolved cations, silica, anions, total dissolved solids (TDS), and total suspended solids (TSS). The results reflected the seasonal variation on discharge, water temperature, and electrical conductivity in the Amoras Stream, with most of the cations, anions, silica TDS, and TSS being carried in the wet season. Partial hydrolysis and silicate incongruent dissolution are the main water/rock interactions in the PC, with an atmospheric/soil CO₂ consumption rate of 1.6 × 10⁵ mol/km²/a. The annual fluxes of Cl⁻, PO₄³⁻, NO₃⁻, and Al³⁺ were significantly influenced from rainwater. Chemical and physical weathering rates were 4 ± 0.8 and 3.0 ± 0.6 m/Ma in the PC, respectively, indicating that under the current climatic condition, the weathering profile is in dynamic equilibrium. Full article

In equatorial and tropical regions, supergene mineral deposits created during water/rock interactions are found. Simply put, these supergene deposits are formed through the accumulation of low solubility ions or through the preservation of primary minerals. The supergene manganese (Mn) deposits are examples of the economic importance associated with the chemical weathering processes. In Brazil, the Southern Brasilia Orogen (SBO) was generated during the collision between the Paranapanema Craton and the passive margin of the São Francisco Craton. In the southern Minas Gerais (MG), several supergene Mn occurrences are hosted in the SBO, which were originated during the chemical weathering of gondites belonging to the Amparo Complex. Here, we studied the supergene Mn occurrences in the southern MG, more specifically in the municipalities of Ouro Fino and Careaçu. The MnO contents ranged from 25.50 to 28.40 wt% at Ouro Fino and from 16.80 to 21.20 wt% at Careaçu. These supergene Mn deposits have a diverse mineral assemblage, being composed of spessartine, quartz, Mn-oxides, goethite and kaolinite. The various Mn minerals formed due to spessartine incongruent dissolution were hollandites, cryptomelanes, romanechites, pyrolusites and lithiophorites. Both study areas are relevant for the possible opening of mines for the commercialization of Mn. Full article

This investigation studies the physical and chemical effect of salt weathering on biocalcarenites and biocalcrudites in the Basilica of Our Lady of Succour (Aspe, Spain). Weathering patterns are the result of salty rising capillary water and water lixiviated from pigeon droppings. Surface modifications and features induced by material loss are observable in the monument. Formation of gypsum, hexahydrite, halite, aphthitalite and arcanite is associated with rising capillary water, and niter, hydroxyapatite, brushite, struvite, weddellite, oxammite and halite with pigeon droppings. Humberstonite is related to the interaction of both types of waters. Analysis of crystal shapes reveals different saturation degree conditions. Single salts show non-equilibrium shapes, implying higher crystallisation pressures. Single salts have undergone dissolution and/or dehydration processes enhancing the deterioration process, particularly in the presence of magnesium sulphate. Double salts (humberstonite) have crystals corresponding to near-equilibrium form, implying lower crystallisation pressures. This geochemical study suggests salts precipitate via incongruent reactions rather than congruent precipitation, where hexahydrite is the precursor and limiting reactant of humberstonite. Chemical dissolution of limestone is driven mainly by the presence of acidic water lixiviated from pigeon droppings and is a critical weathering process affecting the most valuable architectural elements present in the façades. Full article

The Hf-Nd isotope systems are coupled in magmatic systems, but incongruent Hf weathering (‘zircon effect’) of the continental crust leads to a decoupling of the Hf-Nd isotope systems in low-temperature environments during weathering and erosion processes. The Hf-Nd isotope record was recently dated back from the Cenozoic oceans until the Archean, showing that both isotope systems were already decoupled in seawater 2.7 Ga ago and potentially 3.4 Ga and 3.7 Ga ago. While there might have existed a hydrothermal pathway for Hf into Archean seawater, incongruent Hf weathering of more evolved, zircon-bearing uppermost continental crust that was emerged and available for subaerial weathering accounts for a significant decoupling of Hf-Nd isotopes in the dissolved (<0.2 µm) and suspended (>0.2 µm) fractions of Early Earth’s seawater. These findings contradict the consensus that uppermost Archean continental crust was (ultra)mafic in composition and predominantly submerged. Hence, Hf-Nd isotopes in Archean marine chemical sediments provide the unique potential for future research to trace the emergence of evolved continental crust, which in turn has major implications for the geodynamical evolution of Early Earth and the nutrient flux into the earliest marine habitats on Earth. Full article