Major Element Concentrations Research Articles

Assessing Paleoclimate through Major and Trace Element Concentrations: A Review

In geoscience, it is possible to deduce the paleoclimate of sediments from their lithology, fossil content, chemical composition, or geophysical characteristics. In this paper, the author reviewed the use of the concentration of major and trace elements to infer the paleoclimate. For this purpose, a variety of markers have been used in the previous studies, such as CIA, C.I, K2O/Al2O3, Al/Mg, Mg/Ca, Fe/Mn, Rb/Sr, Sr/Cu, Ga/Rb, Sr/Ba, ΣREE, and Eu anomaly. It should be noted that, for a more accurate evaluation of paleoclimate, discrimination diagrams (the plots of K2O+Na2O+Al2O3 versus SiO2, CIA versus C.I, K2O/Al2O3 versus Ga/Rb, Fe/Mn versus Sr/Ba, Rb/Sr versus Sr/Cu, and Mg/Ca-Al/Mg-ΣREE) are the recommended technique

Soil-forming factors controlling Technosol formation in historical mining and metallurgical sites in the high-alpine environment of the Tatra Mountains, southern Poland

The Tatra Mountains are a unique Central European alpine ecosystem where the non-anthropogenic soil cover and soil-forming processes are well recognized. However, the Technosols in the area’s high-mountain environment have not been studied in detail to date. Therefore the aim of this study was to identify the most important soil-forming factors controlling the properties of Technosols developed in historical mining and metallurgical sites in the Tatra Mountains of southern Poland active from the 15th Century until the end of the 19th. The present paper is one of the first attempts to study the genetic aspects of high-mountain Technosols in the temperate climatic zone. The study involved determining soil morphology and classification, soil properties, magnetic susceptibility, mineral composition, optical microscopic observations and total concentration of major elements. The studied Technosols were poorly developed soils with simple soil morphology (mainly A horizon in the topsoil and C horizons in the subsoil). There was a high content of rock fragments. The research has shown that the properties of Technosols in the Tatra Mountains were primarily determined by past human activities like mining and metallurgy as well as the type of anthropogenic parent material, which included mining wastes and metallurgical slags and determined soil properties together with mineral and chemical composition. Soil formation was significantly influenced by vegetation which was conditioned by the relief and climatic conditions dependent on altitudinal zonation. Vegetation and plant-derived soil organic matter shaped topsoil properties. The lengthy soil-forming process acting since a few centuries in some Technosols led to the formation of Bw horizons.

Mineral Composition of Fifteen Species of Asteraceae Family Growing in the Republic of Moldova Using Neutron Activation Analysis

Members of Asteraceae family have properties enabling their application for medical purposes. The major- and microelement content in 15 medicinal species of the Asteraceae family growing in the National Botanical Garden, Republic of Moldova was determined by instrumental neutron activation analysis. A total of 31 chemical elements, Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Br, Rb, Sr, Mo, Sb, Cs, Ba, La, Ce, Sm, Tb, Hf, Ta, Th and U, were identified in herbal samples. Potassium was found to be the most abundant major element; its content in plants ranged from 20,700 mg/kg in Artemisia lerchiana to 58,000 mg/kg in Matricaria recutita. The content of other major elements existed in the following ranges: Ca from 4700 to 14,200 mg/kg and Mg from 1710 to 3870 mg/kg. The maximum content of Mg, K and Ca in analyzed plants was higher compared to data presented in the literature. Among essential microelements the most abundant were Fe (83–910 mg/kg), Mn (23–150 mg/kg) and Zn (27–76 mg/kg). The daily intake of metal and the health risk index for selected elements (As, Ni, Sb, V, Mn, Cr, Co, U, Sr, Al, Fe, and Zn) were calculated. Health risk indexes were obtained for V and Co in Calendula officinalis, Tanacetum balsamita, Achillea clypeolata, Artemisia balchanorum, Artemisia lerchiana, Helichrysum arenarium, and Matricaria recutita. The principal component analysis showed three associations of elements, which can be defined as physiological, geological and anthropogenic sources of elements.

Rifting in the Paleoproterozoic Onega Basin: geochemistry of volcano-sedimentary rocks of the Zaonega Formation

The study of the volcanogenic-sedimentary sequence in the lower part of the Zaonega Formation in the Paleoproterozoic Onega structure (Karelian craton, Fennoscandian Shield) has shown that tuffs and high-silica rocks predominate in its composition. High-silica rocks (SiO2 up to 94 wt. %) are depleted of all elements and probably representing chemogenic siliceous silt. Tuff rocks are close to N-MORB basalts in terms of major element content and rare element distribution character. This association is common to the early stages of continental rifting in the Phanerozoic and may indicate the formation of volcanogenic-sedimentary complexes of the Zaonega Formation in the environment of continental rifting. The mafic rocks in the lower part of the Zaonega Formation are geochemically identical to dolerite dikes and N-MORB-type basalts of 2.10–2.14 Ga age. Their formation was probably related to the same episode of large-scale stretching and thinning of the continental lithosphere of the Karelian craton in the mid–Paleoproterozoic. In this case, the age limit of the Zaonega and underlying Tulomozero Formations should be somewhat older than the 2.06–2.10 Ga interval accepted in modern regional stratigraphic schemes of the Paleoproterozoic of Fennoscandian shield.

Genesis of the Sanhetun Tellurium–Gold Deposit, Northeast China: Constraints from In Situ Elemental and Sulfur Isotopic Compositions of Pyrite

The Sanhetun tellurium–gold (Te–Au) deposit, located in the Duobaoshan polymetallic metallogenic belt (DPMB) within the eastern section of the Central Asian Orogenic Belt (CAOB), is a newly discovered small-scale gold deposit. The mineralization, with a resource of ≥4 t Au, is mainly hosted in three NNE-trending alteration zones between Early Carboniferous granitic mylonite and Lower Cretaceous volcanogenic-sedimentary formations. The genesis of formation of this deposit is poorly constrained. Here, we report the results of petrographic studies, TESCAN Integrated Mineral Analyzer (TIMA), major and trace element concentrations, and in situ S isotopes of pyrite. The results show that there are four types of pyrite: coarse-grained euhedral Py1, fine-grained quartz-Py2 vein crosscutting Py1, anhedral aggregated Py3, and anhedral aggregated Py4. The pre-ore stage Py1 contains negligible Au, Te, and other trace elements and has a relatively narrow range of δ34S values ranging from −1.20 to −0.57‰. Py2 has higher concentrations of Au and Te and distinctly high concentrations of Mo, Sb, Zn, and Mn with markedly positive δ34S values of 4.67 to 14.43‰. The main-ore stage Py3 contains high Au and Te concentrations and shows narrow δ34S values ranging from −5.69 to 0.19‰. The post-ore stage Py4 displays low Au concentrations with the δ34S values ranging from 2.66 to 3.86‰. Tellurides are widespread in Py3 and Py4, consisting mainly of native tellurium, tetradymite, tsumoite, hessite, and petzite. Especially, tetradymite commonly coexists with native gold. This study highlights the role of Te–Bi–S melt as an important gold scavenger in As-deficient ore-forming fluids.

Soil contamination by trace elements and radioelements and related environmental risks in agricultural soils of the M'Dhilla Basin (southwestern Tunisia).

Agricultural soil contaminated by phosphogypsum pile stocked in plan air remains a major problem in M'Dhilla city southwestern of Tunisia. The present effort aimed to enhance the knowledge of trace elements and radioactivity abundance and to assess the corresponding environment. X-ray fluorescence spectroscopy was used to evaluate the trace elements, radioactive elements, and major element concentrations. Our finding revealed that the mean values of U and Th in all the soil profiles ranged from 0.283 to 2.875mg.kg-1 and from 0.797 to 1.491mg.kg-1 respectively. The statistical analyses indicated that uranium abundance has non-significant correlation with the most of trace metals; it shows a moderate correlated with Sr and inverse correlation with P2O5. Contamination factors indicate that the studied soil ranged from uncontaminated to significantly contaminated. Thus, the pollution load index values classify the sites from background values to high pollution sites. The findings of this study will help improve the environmental conditions of M'Dhilla city by addressing contamination issues through targeted interventions. The study's findings highlight the importance of a periodic environmental monitoring such as soil remediation in the study area. This research fills a critical gap in the current understanding of contamination management in this region.

Origin and composition of dissolved and particulate matter in mountain rivers of the Nepal Himalayas: Insights from Sr and Nd isotopes and elemental ratios

The Ganga River exhibits elevated concentrations of dissolved strontium (Sr) and a higher radiogenic Sr (87Sr/86Sr) among global rivers, which impacts oceanic Sr composition. This has implications for understanding weathering and sediment flux into open oceans. The Nepal Himalayan section is a significant part of the upstream Ganga River catchment. We analyzed Sr and Nd isotopes and major element concentrations in water and sediments to trace compositional and seasonal variability in dissolved and particulate matter. The Sr and Nd isotopes, in particular, are crucial in this study as they provide unique signatures that can be used to trace the origin and composition of the dissolved and particulate matter. Representative rivers draining monolithological terrains were selected to investigate the isotopic and elemental provenance and weathering intensity. The elemental ratios (Ca/Na, Mg/Na) indicate the watersheds are carbonate-rich terrains. The Lesser Himalaya (LH) rivers transport radiogenic Sr with high values compared to rivers draining the Tethyan Sedimentary Series (TSS), Higher Himalayan Crystalline (HHC), Mahabharat, and Siwalik Hills. The dry season records a higher 87Sr/86Sr ratio than the monsoon. Due to the faster dissolution of carbonates compared to silicates, monsoon waters transport less radiogenic Sr. The significant correlation of 87Sr/86Sr in dissolved and particulate phases signifies that short-term interactions between sediment and water may alter the 87Sr/86Sr composition. Notably, sediments originating from continental rocks exhibit an inverse correlation between 87Sr/86Sr and εNd. In conclusion, the Sr and Nd isotopic records in this study categorize the fluvial catchments into geological clusters aligned with the TSS, LH, and Siwaliks, which advance our understanding regarding the provenance besides providing crucial insights into geological processes, weathering, landscape evolution, and sediment flux.

Maastrichtian-Cenozoic erosional history of the northern Peruvian Amazonian Andes implications for the Eastern Cordillera evolution (Huallaga Basin, northern Peru)

Late Cretaceous-Cenozoic Andean mountain building may have experienced various phases of orogenesis in response to variations the dip angle of the subducting slab, distinct magmatic pulses, and shortening rates of the orogen. The timing of the Eastern Cordillera (EC) erosion and the relationship between the Andean orogenesis and the establishing of the transcontinental Amazon River remains unclarified. The erosional history of the Amazon Andes and the timing of these orogenic events may be revealed by the late Cretaceous-Cenozoic sedimentary record of the Amazonian retroarc foreland basin. We investigate the provenance of the Maastrichtian-Cenozoic deposits of the Huallaga Basin based on major and trace elements concentrations, SmNd isotopic composition, and UPb zircon dating. We also refined the Oligocene paleoenvironment and calculated Paleogene sedimentation rates. Our results show that despite the 25 Myr-long sedimentary hiatus, both the Maastrichtian and Eocene units show dominant sourcing from the magmatic arc of the Western Cordillera (WC). Increases in Paleozoic and Famatinian zircon grains and a shift toward more negative ƐNd(0) values, indicate dominant EC sources during the Oligocene to middle Miocene. This change in provenance area is Rupelian in age based on the Maximum Likelihood Age (MLA) of JUA22 (29.70 ± 0.62 Ma), suggesting that the onset of Peruvian EC erosion started at ∼30 Ma. The erosion of the EC was accompanied by an increase in sedimentation rates and the development of a meandering fluvial system. Finally, a substantial decrease in zircon grains derived from the Cretaceous and Cenozoic Andean arcs from late Miocene to Recent sediments suggests no contribution of the WC. In contrast, an increase in Paleozoic magmatic arc zircon grains indicates sources in the EC. We compare our findings to constrain the erosional history of the Amazonian Andes and investigate the relationship between the timing of EC uplift and the onset of the transcontinental Amazon drainage system during the Cenozoic.

Mesoproterozoic depleted spinel peridotites metasomatized by high-K hydrous melt in the Patagonian back-arc

Here we report the first investigation of spinel-bearing mantle xenoliths from Los Gemelos volcano, Canquel Plateau, Patagonia. They are highly-depleted Mesoproterozoic (ReOs model ages of 1.3–0.9 Ga) harzburgites and clinopyroxene-poor lherzolites characterized by typical indicators of partial melt extraction, such as low whole-rock Al2O3 and CaO contents (<1.5 wt%), high Mg# of silicate phases (90–95), and Cr-rich spinel (Cr# 0.20–0.42). Depletion of incompatible highly siderophile elements (Re, Ru, Pd) relative to the primitive upper mantle supports high degrees of melt extraction. The occurrence of phlogopite and K-rich alkaline glass veins with high- and low-SiO2 compositions is clear evidence of modal metasomatism. The light rare earth element (LREE) enrichment in clinopyroxene, as well as the whole-rock U-shaped REE pattern, confirms cryptic metasomatism. This melt-rock interaction is corroborated by major (i.e., Mg# vs. basaltic elements) and trace (i.e., La/YbN vs. Sr/Y and Ti/Eu; and Sr vs. Ti/Eu) element contents of pyroxenes. The calculated compositions of melts in equilibrium with clinopyroxene coexisting with phlogopite suggest interaction with slab-derived materials. This metasomatism has been generated by a chromatographic fractionation-reaction process, from deep to shallow mantle domains. The percolation of a high-K hydrous magma probably is associated with the upwelling of asthenospheric material through a slab-window, which caused partial melting of oceanic crust and overlying sediments during the Paleocene. The varying intensities of metasomatic imprints recorded by mantle xenoliths from Los Gemelos provide valuable insights into the interaction of slab-derived materials near the lithosphere-asthenosphere boundary, at a distance of ∼600 km from the Andean volcanic arc.

Genesis of Devonian volcanic-associated Lahn-Dill-type iron ores – part II: trace element fractionation evidences diffuse fluid venting

The iron (Fe)-oxide deposits of the Lahn-Dill-type are composed of haematite-quartz and rare siderite-haematite ores. These ores formed as marine chemical sediments on top of volcaniclastic rocks near the Middle to Late Devonian boundary (∼ 380 Ma). As such, their trace element fractionation patterns provide key information on venting style, ocean chemistry, particle-solution interaction, and depositional environment at the time of ore formation. This study combines WDXRF and ICP-MS/OES whole-rock geochemistry with complementary in-situ LA-ICP-MS analysis, and TEM element mapping of ore samples from the Fortuna Mine (Rhenish Massif, Germany). In-situ measurments were conducted on quartz-haematite, haematite, and siderite-haematite microdomains. Bulk major element contents of the ores indicate (volcani)clastic contamination and post-depositional hydrothermal alteration. Microdomain trace element distributions reveal four different trace element signatures, which are related to: (1) syngenetic apatite formation due to sorption of P and REY from seawater; (2) Fe-(oxyhydr)oxide-specific trace element scavenging and fractionation within the seawater column; (3) diagenetic Fe(III) reduction and trace element mobilisation in pore water; and (4) simultaneous deposition of (volcani)clastic material and Fe-(oxyhydr)oxides. These results show that Lahn-Dill-type iron ore formation resulted from mixing of a low-temperature vent fluid with ambient seawater at high seawater to vent fluid ratios. This likely was related to an environment in which diffuse venting dominated over focused venting, and in which quick Fe-particle precipitation led to formation of haematite-quartz ores. Local diagenetic Fe(III) reduction resulted in post-depositional siderite-haematite ore formation during which trace elements were partially remobilised in pore water.

Assessment of potential toxic elements in soils, sediments, and vegetation in the surroundings of Anapa, Russia.

The study presented here reports the concentration of major, trace, and rare earth elements in soil, sediments, and vegetation samples collected from 13 locations around Anapa City located on the northern coast of the Black Sea in Russia. The neutron activation analysis technique has been used to fulfill this objective. Along with this, the bioconcentration and translocation factors were calculated. Overall, the content of 31 elements was detected in soil and sediments while 20 elements were determined in three types of vegetation: macroalgae (Cystoseira sp. and Ulva sp.), aquatic plants (Phragmites australis), and sea grass (Zostera sp.). The quantified concentration followed the order soil > sediment > vegetation. The phytotoxic levels for Zn, V, Mn, and Fe have been quantified as the highest. Bromine was the most abundant and accumulated in Phragmites australis. Based on the results obtained from this investigation, there is a possibility of contamination in the study area.

Chemical and diatom compositions of dating deep-sea sediment core of the Kuril-Kamchatka Trench, northwestern Pacific

For the first time the grain size, contents of major (Al, Ti, Fe, Mn, Ca, Mg, Na, and K) and trace elements (Mo, Ni, and Cu), total organic carbon, and stable carbon isotope were studied in the sediment cores collected at a water depth of approximately 9500 m from the Kuril-Kamchatka Trench. This study determined the factors of sedimentary environment. The quantitative content and species composition of diatoms were also studied. We have estimated the sedimentation rate based on the excess 210Pb data. According to age models, the sedimentation rate was ∼1.64 mm/year. Paleoconstructions were formed on comparing the distribution of chemical and biological parameters in deep-sea basin sediments. The studied sediments were characterized by the high content of the bioproductivity indicators and chemical elements (Fe, Ca, and Cu) corresponding to a period of increased supply of nutrients that stimulated the production of diatoms. Based on the study of chemical indicators and characteristics of nutrient utilization by phytoplankton, a period of outbreak of diatom productivity due to the introduction of volcanic ash into the sediment in the period 1860–1883 was marked. New data will complement existing information and helpful for further understanding of sedimentary geochemical characteristics in this hadal area, and allow us to relate abiotic conditions to productivity.

EXPERIMENTAL MODELLING OF HYPERGENE PROCESSES FOR BALEY ORE FIELD AS AN EXAMPLE

Samples of primary low-sulphide gold-quartz ore and oxidised host rock containing up to 10 wt% sulphides and 5 wt% their oxidation products were investigated to reveal the relationship between the migration of elements during the hypergenic transformation of ores and rocks and their mineral composition. Mineralogical studies employed optical and electron microscopy to identify the shapes and sizes of mineral individuals and aggregates and to determine their chemical composition. It is determined for major element content that the oxidised host rocks contain significantly more iron, sulphur, aluminium, potassium and phosphorus than primary low-sulphide quartz gold ores, while silicon and calcium content is lower. This is due to the removal of sulphur and iron into the near-vein rocks with the formation of primarily pyrite and arsenopyrite, and the presence of aluminosilicates (feldspars and layered silicates) in them. The same applies to arsenic and antimony, as their concentrations are higher in the host rocks than in the ores. The rates of lithophile elements recovery from primary gold-quartz ores are much higher than those from oxidised host rocks. Сhalcophile elements, on the contrary, are more intensively transferred to the solution from host rocks. Thus, the complex of elements extracted from ore suspensions is directly determined by their mineral composition. The main carrier of gold is native gold and its tellurides. Silver is associated with low-grade gold, copper and silver sulphosalts, and also tellurides.

Magmatic evolution and sources of metals and fluids in the large granite-related Xiasai vein-type Ag–Pb–Zn(–Sn) deposit, northern Yidun terrane, SW China

The Xiasai Ag–Pb–Zn–(Sn) deposit in the northern Yidun terrane (eastern Tethys), hosted in Late Triassic metasandstones, is genetically associated with Late Cretaceous granites. We present chemical and Sr–Nd–Pb–Li–B isotope data of Late Cretaceous granites and their mafic microgranular enclaves (MME), late aplites, and Late Triassic metasedimentary rocks. The narrow range of 87Sr/86Sr99 (0.70627–0.70953) and εNd99 (–6.1 to –5.2) values of most Late Cretaceous granites reflects a mixed source with contributions from the mantle and Paleoproterozoic felsic crust. These granites have high SiO2 contents (>69 wt%) and strong depletions in Sr, Ba, and Eu. Major and trace element contents correlate with the fractionation index 1/TiO2, indicating that they experienced extensive fractionation. Local late aplite dikes were derived from similar source rocks, but seem to be younger.The Pb isotopic compositions reflect that the metal Pb was derived from the granite with variable contributions from the Late Triassic sedimentary rocks. Weakly and moderately altered metasandstones have similar δ7Li and δ11B values as most granites (δ7Li: 0.00 to 2.68 ‰; δ11B values: –14.93 to –12.36 ‰), indicating magmatic fluid sources. The magmatic fluids resulted in the initial enrichment of Sn, Cu, Pb, and Zn. Strong alteration of feldspar and biotite resulted in the metasandstones in negligible change of Li concentrations, significant loss of Sr, Na2O, CaO, MgO, and Fe2O3, but significant addition of B. This alteration lowered δ7Li from 1.01 to –3.65 ‰ and lowered δ11B from –9.43 to –19.18 ‰. The low δ7Li values and extremely low δ11B values reflect external fluids from the Late Triassic sedimentary wall rocks, which interacted with granites and mobilized metals (e.g., Sn, Ag, Pb, and Zn) from the granite and/or the sedimentary wall rocks. The location of the Xiasai deposit is controlled by regional NNW-trending faults induced by Late Cretaceous extension.

Application of nanofiltration for the recovery of nickel glycinates from alkaline glycine-based solutions using polyamide membranes: A technical note

Glycine has been intensively investigated as a “green” lixiviant for precious and base metals. Alkaline glycine solutions to extract Ni from sulfide resources has shown promising results. However, a considerable amount of Ni will be lost in the wash solutions when leaching residues are washed during solid-liquid separation of the leachates from their respective leach residues. In this context, this study explored Ni recovery from alkaline glycine-based wash solutions using a polyamide nanofiltration membrane. In the tests using synthetic single and multi-metal solutions, the membrane achieved >95% rejection of Ni in the selected ranges of glycine/Ni molar ratio (up to 5), pressure (15–30 bar), initial nickel concentration (0.5–1.5 g/L), sodium sulfate background concentration (∼30 g/L) and under the use of different pH modifiers (aqueous ammonia and caustic soda). When using a real solution, the concentrations of Ni and other major elements (Cu, S, Co, Mg, Zn) in the final retentate increased by about 5 times at 80 wt% permeate recovery, leaving <3 mg/L major elements in permeate. The permeate stream could be recycled in the washing stage, and the retentate stream could be combined with the pregnant leach solution (PLS) for metals recovery. The investigation demonstrates some of the technical optionality for nickel recovery from filter wash solutions utilising nanofiltration within the context of alkaline glycine-based leach technology and preliminarily demonstrates where it can be used in the structure of flowsheets to recover valuable base metals and reagents for recycle. However, the increased membrane resistance causing a low permeate flux should be concerned due to the considerable dissolved salts, precipitation of gypsum and the increasing feed concentration over time.

Industrial Deportment of Minor and Trace Elements in Direct Nickel Matte Smelting

A sampling campaign was carried out at an industrial nickel flash smelter with the aim of evaluating the trace element distributions along the smelting line from raw materials to high-grade nickel matte and discard slag. The industrial technology was direct-to-nickel matte smelting without conventional Peirce–Smith converters, thus having two different nickel mattes as smelting products and feeds in the refinery: the sulfidic low-iron nickel matte from smelting furnace and the low-sulfur electric furnace matte from slag cleaning. Major and trace element concentrations were obtained from the solidified samples by electron probe microanalysis and laser ablation–inductively coupled plasma–mass spectrometry. Due to the industrial sampling environment, i.e., the slow cooling rate of the samples, not all the trace element concentrations were able to be measured at the lowest detection limits of the techniques used in some of the phases formed after cooling. However, the obtained results and element distribution coefficients were in good agreement with equilibrium values published in the literature.

Pre-hispanic wetland irrigation and metallurgy in the South Andean Altiplano (Intersalar Region, Bolivia, XIVth and XVth century CE)

The high-altitude Andean Altiplano has been subject to abrupt climate changes during the Holocene. The resulting impact on the hydrological cycle has obliged ancient societies to adapt and develop strategies to face droughts and sustain agropastoral activities. Here, we present the results of archaeological prospections together with the biogeochemical characterization of a well-dated core collected at Saitoco wetland in the arid southern Altiplano (Intersalar Region, Bolivia). Archaeological survey allowed the mapping of a network of channels collecting water from the surrounding mountains to the wetland, and the presence of small copper mines and metallurgical installations. Traces and major element concentrations and accumulation rates, together with elemental and isotopic characterization of organic matter (OM) (i.e., Corg and δ13Corg) in the wetland core have been used to document the evolution of the landscape in relation to climatic and anthropogenic pressure. While OM, bromine (Br), selenium (Se) and mercury (Hg) data were used to assess the variability of precipitations during the Late Holocene (4.2 ka BP to the present), local and regional mining activities have been reconstructed through the variations of lead (Pb), copper (Cu), and antimony (Sb). Our results show an abrupt change in OM composition during the 14th and 15th century CE, characterized by an abrupt shift in δ13Corg synchronous with a rise in Br, Se and Hg, testifying for the waterlogging of the wetland during a known arid period in the region. This change is attributed to anthropogenic transformation of the landscape through the irrigation of the wetland by channeling streams from the surrounding mountains. At the same time, a mining pollution signal was recorded supporting local Cu mining and metallurgy. The mining signal then reached its maximum values during the Inca and Colonial periods, which matches with reported enhanced mining activities in the region. From the colonial era onward, the wetland progressively dried up, likely resulting from the abandonment of the site. Through the combination of a biogeochemical record and archaeological prospections, this study provides evidences that societies of the arid Intersalar region have transformed their landscape and developed wetland irrigation and mining during the arid 14th and 15th century CE Period.

Evolution of Physical and Chemical Characteristics of Atmospheric Precipitation and Its Significant Impacts on the Environment in Beijing

Atmospheric precipitation samples were collected in 2018, 2019, and 2021 in Beijing to study the concentrations and changes of the main metal elements and water-soluble ions； the wet deposition fluxes of heavy metals, water-soluble ions, dissolved inorganic nitrogen, and sulfur in the atmospheric precipitation and their impacts on the ecological environment； and the scavenging mechanisms of the typical precipitation to atmospheric pollutants during the study period. The results showed that the precipitation in Beijing during the study period was mostly neutral or alkaline, and the frequency of acid rain occurrence was very low, only accounting for 3.06%. The total concentrations of major metal elements in 2018, 2019, and 2021 were （4 787.46 ±4 704.31）, （7 663.07 ±8 395.05）, and （2 629.13 ±2 369.51） μg·L-1, respectively. The total equivalent concentrations of ions in 2018, 2019, and 2021 were （851.68 ±649.16）, （973.98 ±850.94）, and （644.31 ±531.16） μeq·L-1, respectively. The interannual changes in major metal elements and ions followed the order of 2019 &gt; 2018 &gt; 2021. The seasonal average total concentrations of major metal elements in spring, summer, autumn, and winter were （9 624.25 ±7 327.92）, （4 088.67 ±5 710.14）, （3 357.68 ±3 995.64）, and （6 203.19 ±3 857.43） μg·L-1, respectively, and the seasonal average total equivalent concentrations of ions in spring, summer, autumn, and winter were （1 014.71 ±512.21）, （729.83 ±589.90）, （724.35 ±681.40）, and （1 014.03 ±359.67） μeq·L-1, respectively, all presenting the order of spring &gt; winter &gt; summer &gt; autumn. NO3- and SO42- were the main acid-causing ions in precipitation, whereas NH4+ and Ca2+ were the main acid-neutralizing ions. The wet deposition fluxes of the heavy metal Cd were very low [（0.05 ±0.01） mg·（m2·a）-1], only accounting for （0.13 ±0.04）% of the total wet deposition fluxes of main metal elements； however, its soil safety years were 291 years, significantly lower than those of other heavy metals, displaying that its ecological risk was relatively the highest. The total wet precipitation flux of water-soluble ions NH4+, Ca2+, NO3-, and SO42- accounted for （85.72 ±2.18）% of the wet precipitation flux of total ions, suggesting that their comprehensive impact on the ecological environment might have been higher. DIN wet deposition flux was mainly characterized by NH4+-N, which had a positive impact on the ecological environment in summer. SO42--S wet deposition flux was higher in summer, so its positive impact on the ecological environment was also greater. The scavenging effects of atmospheric precipitations to pollutants from the air were impacted by various factors, and the synergism effects of these factors could directly influence the scavenging mechanisms of precipitation to pollutants.

Formation and hydrothermal alteration of a volcanic center: Melt pooling and mass transfers at Langseth Ridge (Gakkel Ridge, Arctic Ocean)

Volcanic centers are characteristic features of ultraslow-spreading mid-ocean ridges, the least-explored parts of the global ridge system. Volcanic centers can provide insights into deep magmatic and metamorphic processes at these ridges. Here, we present data from the largest volcanic center on the Gakkel Ridge, the Langseth Ridge, situated at 60–62°E. Langseth is ∼10 km wide, consisting of three peaks that rise to 585 m water depth, some 3–4 km above the surrounding seafloor. It strikes perpendicular to Gakkel's spreading direction and can be traced for ∼40 km, which translates to an age of ∼8 Myr. Seafloor imaging revealed abundant (pillow) basalt but also fissures and geologic faults across the Langseth Ridge. Basaltic rocks were sampled at all summits and diabase at the slope of the northern summit that dips into the rift valley.Our samples are of normal to depleted mid-ocean ridge basalt composition and exhibit a wide range of major and trace element contents, due to magmatic processes, accumulation of macrocrysts, and hydrothermal alteration. Radiogenic isotope ratios, most notably 143Nd/144Nd and 208Pb/206Pb, trend from typical rift valley compositions to isotopically enriched values with increasing distance to the rift valley. This trend may imply melt pooling from different sources, potentially representing a shift from shallow melting beneath the rift valley to deeper melting of enriched sources and higher degrees of melting underneath Langseth. Mineral compositions and plagioclase sieve textures imply prolonged storage of magma at depth prior to eruption. Hydrothermal alteration occurred over a range of conditions. Basalt from the summits is weakly altered at temperatures ≪100 °C, which likely occurred in situ at the summit sites. Diabase samples experienced chloritization and albitization and display epidote and quartz veins, which formed at >300 °C. These assemblages and temperatures are typical for lower crustal levels and imply uplift of the samples of >1 km. Diabase samples from the Afanasenkov Seamount, another volcanic center on the Gakkel Ridge that we investigated for comparison, were altered under comparable conditions.Our findings suggest a combined volcanic–tectonic origin of the studied volcanic centers, potentially implying that such complexes may generally form due to the interplay of magmatism and tectonics. Researching volcanic centers has the potential to further our understanding of both deep and shallow crustal processes at ultraslow-spreading ridges, providing further insights into the role of these centers as linkages between lithosphere and hydrosphere and the (deep) biosphere they sustain.

A survey study on arsenic speciation in coal fly ash and insights into the role of coal combustion conditions

Coal fly ashes (CFAs) are the low-density byproducts of the coal combustion process. Improper or uncontrolled CFA disposal poses significant environmental and health concerns due to the potential leaching of toxic heavy metals such as arsenic (As). Previous studies have investigated the content and speciation of As in different CFA samples, yet systematic information on As speciation in CFA with representative coal source and combustion conditions is still missing. Based on a recent survey study on the typical coal sources and combustion conditions across the U.S., this study selected 19 representative CFA samples to systematically investigate As speciation and potential correlations with these parameters. The composition, morphology, mineralogy, and As speciation of these CFA samples were characterized by complementary analytical, microscopic, and spectroscopic techniques. Synchrotron X-ray spectroscopy and microscopy analyses revealed the dominant As oxidation state to be As(V) and with strong associations to Ca, with the exception of 3 samples that had 19–51% As(III), likely due to the use of selective catalytic reduction (SCR) process. Principal component analysis was conducted to identify potential correlations of As concentration and oxidation state with parameters such as major element content, loss on ignition (LOI), average particle size, coal source, and combustion condition. Al2O3 and FeO content were found to capture a majority of the variability. Results from this study provide fundamental basis for understanding the correlations between coal source, combustion conditions, CFA characteristics, and As speciation, and providing insights for downstream beneficial utilization or disposal management.