Search

In an effort to combat the threat of drought, China constructed the South-to-North Water Transfer Project (SNWTP), the biggest water transfer project in terms of volume with the largest beneficiary population in the world. Reports have shown that massive water diversion projects have had detrimental environmental consequences including water quality decline and freshwater habitat degradation. However, few reports have assessed the impact of the transfer project on sediment quality, which is highly susceptible to allogenic and local anthropogenic pollution. We examined the distribution characteristics of Cd, Cr, Cu, Ni, Pb and Zn in surface sediment of the largest reservoir along the East Route of SNWTP, Nansihu Lake, followed by positive matrix factorization (PMF) to determine their potential sources. We utilized enrichment factor, multiple sediment quality guidelines (SQGs), and potential ecological risk index (RI) to determine metal accumulation or pollution risk. The results show the mean concentrations of Cr, Cu, Pb, Zn were slightly lower than in samples collected in 2003, 2010 and 2012, while the mean concentrations of Cr and Ni were significantly higher than samples from previous years. Among the six metals, Cr, Cu and Ni are of higher ecological risk according to SQGs; but Cd is of higher ecological risk according to RI. PMF analysis shows that industrial production and shipping are important sources of Cr, Cu, and Ni. PMF analysis also shows that a considerable amount of trace metals, especially Cd, Cr, Pb and Zn, mainly comes from the use of pesticide fertilizers and biomass sources in farmland, and may partly enter Nansihu Lake from SNWTP. This study reveals the possible sources of trace metals to the Nansihu Lake which is part of SNWTP; the results of the study may serve as a reference for better understanding the impact of future water diversion projects on metals distribution. Unlabelled Image • Water transfer is likely a new source of trace metals in sediment of Nansihu Lake. • Industry and agricultural sources contributed to metals in the lake significantly. • Pollutions are expected to occur especially from Cr, Cu, Ni and Pb according to SQGs. • Cd posed a considerable potential ecological risk according to RI. • SQGs and RI are short for pollution or ecological risk assessment methods. [ABSTRACT FROM AUTHOR]

Providing access to safe drinking water is a global challenge, for which groundwater is increasingly being used throughout the world. However, geogenic contaminants limit the suitability of groundwater for domestic purposes over large geographic areas across most continents. Geogenic contaminants in groundwater are often evaluated individually, but here we demonstrate the need to evaluate multiple contaminants to ensure that groundwater is safe for human consumption and agricultural usage. We compiled groundwater chemical data from three aquifer regions across the world that have been reported to have widespread As and Mn contamination including the Glacial Aquifer in the U.S., the Ganges-Brahmaputra-Mehta Basin within Bangladesh, and the Mekong Delta in Cambodia, along with newly sampled wells in the Yangtze River Basin of China. The proportion of contaminated wells increase by up to 40% in some cases when both As and Mn contaminants are considered. Wilcoxon rank-sum analysis indicates that Mn contamination consistently occurs at significantly shallower depths than As contaminated wells in all regions. Arsenic concentrations in groundwater are well predicted by redox indicators (Eh and dissolved oxygen) whereas Mn shows no significant relationship with either parameter. These findings illustrate that the number of safe wells may be drastically overestimated in some regions when Mn contamination is not taken into account and that depth may be used as a distinguishing variable in efforts to predict the presence of groundwater contaminants regionally. [ABSTRACT FROM AUTHOR]

Consumption of groundwater containing >10 µg L-1 arsenic (As) adversely impacts more than 100 million people worldwide. Multiyear trends in aquifer As concentrations have been documented, but strong seasonal variations are not commonly observed. Here we report dramatic seasonal changes in As concentrations and aquifer chemistry within the Jianghan Plain of the Yangtze River, China. At some wells, concentrations fluctuate by more than an order of magnitude within a single year (100-1200 µg L-1). Groundwater extraction and sustained water levels of surface channels during the dry season induces a strong downward hydraulic gradient, seasonally supplying oxidizing (oxygen, nitrate) water to the otherwise anoxic aquifer. Oxygen and/or nitrate addition promotes a transient drop in As concentrations for 1-3 months. When recharge ceases, reducing, low-arsenic conditions are reestablished by reactive, endogenous organic carbon. Temporal variability in As concentrations is especially problematic because it increases the probability of false-negative well testing during low-arsenic seasons. However, periods of low As may also provide a source of less toxic water for irrigation or other uses. Our results highlight the vulnerability and variability of groundwater resources in the Jianghan Plain and other inland basins within Asia to changing geochemical conditions, both natural and anthropogenic, and reinforce that continued monitoring of wells in high-risk regions is essential. [ABSTRACT FROM AUTHOR]

Abstract: The aggregate-based structure of soils imparts physical heterogeneity that gives rise to variation in microbial and chemical processes which influence the speciation and retention of trace elements such as As. To examine the impact of distributed redox conditions on the fate of As in soils, we imposed various redox treatments upon constructed soil aggregates composed of ferrihydrite- and birnessite-coated sands presorbed with As(V) and inoculation with the dissimilatory metal reducing bacterium Shewanella sp. ANA-3. Aeration of the advecting solution surrounding the aggregates was varied to simulate environmental conditions. We find that diffusion-limited transport within high dissolved organic carbon environments allows reducing conditions to persist in the interior of aggregates despite aerated advecting external solutes, causing As, Mn, and Fe to migrate from the reduced aggregate interiors to the aerated exterior region. Upon transitioning to anoxic conditions in the external solutes, pulses of As, Mn and Fe are released into the advecting solution, while, conversely, a transition to aerated conditions in the exterior resulted in a cessation of As, Mn, and Fe release. Importantly, we find that As(III) oxidation by birnessite is appreciable only in the presence of O2; oxidation of As(III) to As(V) by Mn-oxides ceases under anaerobic conditions apparently as a result of microbially mediated Mn(IV/III) reduction. Our results demonstrate the importance of considering redox conditions and the physical complexity of soils in determining As dynamics, where redox transitions can either enhance or inhibit As release due to speciation shifts in both sorbents (solubilization versus precipitation of Fe and Mn oxides) and sorbates (As). [Copyright &y& Elsevier]

Abstract: Manganese (Mn) and iron (Fe) oxides are ubiquitous solids in terrestrial systems that have high sorptive capacities for many trace metals, including arsenic (As). Although numerous studies have characterized the effects of As adsorption onto Fe and Mn oxides individually, the fate of arsenic within mixed systems representative of natural environments has not been completely resolved. Here, we examine oxidation and competitive retention of As on goethite and birnessite using a Donnan reactor, where each oxide is isolated by a semi-permeable membrane through which arsenic can migrate. To initiate the Donnan reactor experiments, As(III) was simultaneously added to both chambers. Arsenic(III) injected into the birnessite chamber is rapidly oxidized to As(V) and then slowly redistributes across both chambers, while that added to the goethite chamber undergoes rapid adsorption; the adsorbed As(III) on goethite subsequently undergoes desorption and diffusion into the birnessite chamber followed by oxidation to As(V). With increased reaction time, As(V) is generated and preferentially partitioned onto goethite due to higher adsorption affinity compared to birnessite. Furthermore, the dissolved concentration of As(V) is controlled by the adsorption capacity of the goethite surface, which when saturated, leads to increased aqueous As concentrations; despite an increase in As(V) loading on birnessite with increasing initial As(III) concentration, the resulting aqueous As(V) concentration increase appreciably once the goethite surface is saturated. Our findings show that Mn oxides in soils act as a temporary sorbent of As, but operate primarily as strong oxidants responsible for transformation of As(III) to As(V), which can then strongly adsorb on the surrounding Fe oxide matrix. [Copyright &y& Elsevier]

The speciation and partitioning of arsenic (As) in surface and subsurface environments are controlled, in part, by redox processes. Within soils and sediments, redox gradients resulting from mass transfer limitations lead to competitive reduction—oxidation reactions that drive the fate of As. Accordingly, the objective of this study was to determine the fate and redox cycling of As at the interface of birnessite (a strong oxidant in soil with a nominal formula of MnOx, where x ≈ 2) and dissimilatory As(V)-reducing bacteria (strong reductant). Here, we investigate As reduction-oxidation dynamics in a diffusively controlled system using a Donnan reactor where birnessite and Shewanella sp. ANA-3 are isolated by a semipermeable membrane through which As migrates. Arsenic(III) injected into the reaction cell containing birnessite is rapidly oxidized to As(V). Arsenic(V) diffusing into the Shewanella chamber is then reduced to As(III), which subsequently diffuses back to the birnessite chamber, undergoing oxidation, and establishing a continuous cycling of As. However, we observe a rapid decline in the rate of As(III) oxidation owing to passivation of the birnessite surface. Modeling and experimental results show that high [Mn(II)] combined with increasing [CO32-] from microbial respiration leads to the precipitation of rhodochrosite, which eventually passivates the Mn oxide surface, inhibiting further As(III) oxidation. Our results show that despite the initial capacity of birnessite to rapidly oxidize As(III), the synergistic effect of intense As(V) reduction by microorganisms and the buildup of reactive metabolites capable of passivating reactive mineral surfaces—here, birnessite—will produce (bio)geochemical conditions outside of those based on thermodynamic predictions. [ABSTRACT FROM AUTHOR]

• The Fe-rich tailings adsorbed high Mn contents in its way to the estuary. • Redox fluctuations led to precipitation of Mn oxides and poorly crystalline Fe oxides. • Both Mn and Fe reduction in estuarine soils increased Mn contents in water. • Dissolved Mn increased in 880% posing a risk to environmental and human health. Manganese (Mn) is an abundant element in terrestrial and coastal ecosystems and an essential micronutrient in the metabolic processes of plants and animals. Mn is generally not considered a potentially toxic element due to its low content in both soil and water. However, in coastal ecosystems, the Mn dynamic (commonly associated with the Fe cycle) is mostly controlled by redox processes. Here, we assessed the potential contamination of the Rio Doce estuary (SE Brazil) by Mn after the world's largest mine tailings dam collapse, potentially resulting in chronic exposure to local wildlife and humans. Estuarine soils, water, and fish were collected and analyzed seven days after the arrival of the tailings in 2015 and again two years after the dam collapse in 2017. Using a suite of solid-phase analyses including X-ray absorption spectroscopy and sequential extractions, our results indicated that a large quantity of MnII arrived in the estuary in 2015 bound to Fe oxyhydroxides. Over time, dissolved Mn and Fe were released from soils when FeIII oxyhydroxides underwent reductive dissolution. Due to seasonal redox oscillations, both Fe and Mn were then re-oxidized to FeIII, MnIII, and MnIV and re-precipitated as poorly crystalline Fe oxyhydroxides and poorly crystalline Mn oxides. In 2017, redox conditions (Eh: −47 ± 83 mV; pH: 6.7 ± 0.5) favorable to both Fe and Mn reduction led to an increase (~880%) of dissolved Mn (average for 2015: 66 ± 130 µg L-1; 2017: 582 ± 626 µg L-1) in water and a decrease (~75%, 2015: 547 ± 498 mg kg−1; 2017: 135 ± 80 mg kg−1) in the total Mn content in soils. The crystalline Fe oxyhydroxides content significantly decreased while the fraction of poorly ordered Fe oxides increased in the soils limiting the role of Fe in Mn retention. The high concentration of dissolved Mn found within the estuary two years after the arrival of mine tailings indicates a possible chronic contamination scenario, which is supported by the high levels of Mn in two species of fish living in the estuary. Our work suggests a high risk to estuarine biota and human health due to the rapid Fe and Mn biogeochemical dynamic within the impacted estuary. [ABSTRACT FROM AUTHOR]

Emerging evidence points out that the responses of soil organic carbon (SOC) to nitrogen (N) addition differ along the soil profile, highlighting the importance of synthesizing results from different soil layers. Here, using a global meta‐analysis, we found that N addition significantly enhanced topsoil (0–30 cm) SOC by 3.7% (±1.4%) in forests and grasslands. In contrast, SOC in the subsoil (30–100 cm) initially increased with N addition but decreased over time. The model selection analysis revealed that experimental duration and vegetation type are among the most important predictors across a wide range of climatic, environmental, and edaphic variables. The contrasting responses of SOC to N addition indicate the importance of considering deep soil layers, particularly for long‐term continuous N deposition. Finally, the lack of depth‐dependent SOC responses to N addition in experimental and modeling frameworks has likely resulted in the overestimation of changes in SOC storage under enhanced N deposition. [ABSTRACT FROM AUTHOR]

Abstract Hypersaline tidal flats (HTF) are transitional ecosystems which play an important role over Si biogeochemistry in wetlands. Sources and sinks of Si in these ecosystems are directly dependent on pedogenesis and are strongly influenced by the readily soluble Si components, such as dissolved Si, adsorbed Si, and amorphous silicates. The aim of this study was to identify and assess the distribution of readily soluble Si pool in two HTFs on the Brazilian coast. We based our studies on sequential extractions of iron and silicon, modeling of the soil aqueous phase, and X-ray diffraction of the fine clay fraction. Our results show that mobile Si and adsorbed Si are present at very low levels in HTF soils, comprising <3% of the readily soluble Si pool. Silicon associated with Fe oxyhydroxides is the second largest component of the readily soluble Si pool, making up 8.7–40.8% of the Si extractions. The correlation between the ferrihydrite fraction and Si associated with Fe oxyhydroxides indicates a large control of Si by ferrihydrite. Amorphous Si makes up the dominant fraction, comprising 59–90% of the Si extractions. SEM images show the presence of diatoms, sponges, and phytoliths in the soils. Precipitation of pedogenic opal seems to occur in the soils due to a dry season at both sites. The clay assemblages are composed of the mixed-layer kaolinite-smectite (K-S), kaolinite-illite (K-I), and illite-smectite (I-S), and lesser amounts of kaolinite (K) and smectite (S) end-members. The presence of these clays indicates that HTF soils are conducive to the formation of mixed-layer minerals, which partially control Si dynamics. Our data indicate that HTF soils tend to accumulate Si by adsorption, (co)precipitation, and reactions involving clay minerals. [ABSTRACT FROM AUTHOR]

Hypersaline tidal flats (HTFs) represent transitional ecosystems where the ocean, land, and freshwater meet. These places are globally widespread and their soils are an important environmental component controlling chemical reactions in wetland ecosystems. Here, we present a pedogenic study of two HTFs on the Brazilian coast (northeast and southeast) based on the solid-phase geochemistry of Fe and Mn and morphological studies. Broken and irregular topographies and strong expression of redoximorphic concentrations (e.g., mottles, nodules, and pore linings) are present throughout the soil profiles. Although lepidocrocite is the most abundant Fe fraction in these soils (more than 50% of all extractions), deeper horizons show pyrite as the main Fe fraction caused by the presence of buried mangrove soils. The more oxidizing conditions in these deeper horizons indicate that pyrite is not stable and is undergoing degradation. Iron released in this process is moving upward and precipitating as Fe oxides in more oxidized portions of the soil profile. Coprecipitation of Mn and ferrihydrite seems to be an important process controlling the geochemistry of Mn in HTFs. Our data indicate that deeper horizons have been transforming, driven mainly by water table oscillation and, consequently, redox processes. This process allows translocation of Mn2+ and Fe2+ throughout the soil profile, followed by oxidation and precipitation of Mn3+/4+ and Fe3+ oxides in preferential sites. [ABSTRACT FROM AUTHOR]

The composition of ambient particulate matter (PM) and its sources were investigated at the Salton Sea, a shrinking saline lake in California. To investigate the influence of playa exposure on PM composition, PM samples were collected during two seasons and at two sites around the Salton Sea. To characterize source composition, soil samples were collected from local playa and desert surfaces. PM and soil samples were analyzed for 15 elements using mass spectrometry and X-ray diffraction. The contribution of sources to PM mass and composition was investigated using Al-referenced enrichment factors (EFs) and source factors resolved from positive matrix factorization (PMF). Playa soils were found to be significantly enriched in Ca, Na, and Se relative to desert soils. PMF analysis resolved the PM10 data with four source factors, identified as Playa-like, Desert-like, Ca-rich, and Se. Playa-like and desert-like sources were estimated to contribute to a daily average of 8.9% and 45% of PM10 mass, respectively. Additionally, playa sources were estimated to contribute to 38-68% of PM10 Na. PM10 Se concentrations showed strong seasonal variations, suggesting a seasonal cycle of Se volatilization and recondensation. These results support the importance of playas as a source of PM mass and a controlling factor of PM composition. [ABSTRACT FROM AUTHOR]

Increased human‐derived nitrogen (N) loading in terrestrial ecosystems has caused widespread ecosystem‐level phosphorus (P) limitation. In response, plants and soil micro‐organisms adopt a series of P‐acquisition strategies to offset N loading‐induced P limitation. Many of these strategies impose costs on carbon (C) allocation by plants and soil micro‐organisms; however, it remains unclear how P‐acquisition strategies affect soil C cycling. Herein, we review the literature on the effects of N loading on P limitation and outline a conceptual overview of how plant and microbial P‐acquisition strategies may affect soil organic carbon (SOC) stabilization and decomposition in terrestrial ecosystems.Excessive input of N significantly enhances plant biomass production, soil acidification, and produces plant litterfall with high N/P ratios, which can aggravate ecosystem‐level P limitation.Long‐term N loading can cause plants and soil micro‐organisms to alter their functional traits to increase P acquisition. Plants can release carboxylate exudates and phosphatases, modify root morphological traits, facilitate the formation of symbiotic associations with mycorrhizal fungi and stimulate the abundance of P‐mineralizing and P‐solubilizing micro‐organisms. Releasing carboxylate exudates and phosphatases could accelerate SOC decomposition, whereas changing symbiotic associations and root morphological traits (e.g. an increase in fine root length) may contribute to higher SOC stabilization. Increased relative abundances of P‐mineralizing and P‐solubilizing bacteria can accelerate P mining and SOC decay, which may decrease microbial C use efficiency and subsequently lower SOC sequestration.The trade‐offs between different plant P‐acquisition strategies under N loading should be among future research priorities due to their cascading impacts on soil C storage. Quantifying ecosystem thresholds for P adaption to increased N loading is important because P‐acquisition strategies are effective when N loading is below the N threshold. Moreover, understanding the response of P‐acquisition strategies at different levels of native soil N availability could provide insight to divergent P‐acquisition strategies across sites and ecosystems. Altogether, P‐acquisition strategies should be explicitly considered in Earth System Models to generate more realistic predictions of the effects of N loading on soil C cycling. Read the free Plain Language Summary for this article on the Journal blog. [ABSTRACT FROM AUTHOR]

As coastal ecosystems become widely recognized for their capacity to sequester carbon (blue carbon), standard accounting methodologies for the generation of carbon credits are being developed. To ensure the applicability of these standards across blue carbon ecosystems, we investigated organic carbon provenance and burial in salt marshes and seagrass meadows of an arid, upwelling‐dominated Eastern Pacific lagoon. We found low carbon density in benthic sediments of Bahía de San Quintín (5.9 ± 0.5 mg C cm−3), only marginally higher in Zostera marina beds (6.9 ± 0.5 mg C cm−3), likely due to remineralization and hydrodynamically driven export of seagrass material, resulting in low carbon burial rates (4.5 ± 2.5 g C m−2 yr−1). Sediment organic carbon is mainly controlled by the fraction of fine sediment and its source is largely allochthonous, although sources differ spatially. Salt marshes at San Quintín derive 40% of their organic matter from autochthonous material and exhibit higher carbon burial rates (up to 414.7 ± 28.6 g C m−2 yr−1) and sediment carbon densities (32.0 ± 0.7 mg C cm−3) compared to benthic sediments. This study emphasizes the connectivity of blue carbon habitats with marsh plant detritus supplementing benthic carbon burial and incorporation of detrital eelgrass in marsh sediments. Our findings highlight the importance of allochthonous organic matter for carbon sequestration in blue carbon habitats, suggesting standard accounting practices that deduct allochthonous organic matter would miss the full potential for carbon burial. [ABSTRACT FROM AUTHOR]

Abstract: Preventing the release of mercury from coal-fired power plants continues to be a challenge. The design of effective and affordable control strategies depends upon the speciation of mercury from the high temperature region of the boiler to the lower temperature environment of the stack. Both homogeneous and heterogeneous oxidation pathways play a role in determining mercury''s speciation over the temperature range of coal-fired flue gas. This review explores the current state of knowledge associated with the kinetically-limited homogeneous reaction pathways in addition to the complexities associated with heterogeneous oxidation processes. In particular, oxidation pathways associated with selective catalytic reduction and precious metal catalysts are considered. In addition, adsorption mechanisms on various materials are discussed, including fly ash and activated carbon for flue gas applications and precious metals for fuel gas applications. [Copyright &y& Elsevier]

Increased human‐derived nitrogen (N) deposition to terrestrial ecosystems has resulted in widespread phosphorus (P) limitation of net primary productivity. However, it remains unclear if and how N‐induced P limitation varies over time. Soil extracellular phosphatases catalyze the hydrolysis of P from soil organic matter, an important adaptive mechanism for ecosystems to cope with N‐induced P limitation. Here we show, using a meta‐analysis of 140 studies and 668 observations worldwide, that N stimulation of soil phosphatase activity diminishes over time. Whereas short‐term N loading (≤5 years) significantly increased soil phosphatase activity by 28%, long‐term N loading had no significant effect. Nitrogen loading did not affect soil available P and total P content in either short‐ or long‐term studies. Together, these results suggest that N‐induced P limitation in ecosystems is alleviated in the long‐term through the initial stimulation of soil phosphatase activity, thereby securing P supply to support plant growth. Our results suggest that increases in terrestrial carbon uptake due to ongoing anthropogenic N loading may be greater than previously thought. [ABSTRACT FROM AUTHOR]

• C in soils across a single furrow irrigated orchard were assessed in soils with contrasting wet-dry cycling frequencies. • CO 2 efflux in repeated wet-dry soils from furrow irrigation is diffusion controlled. • SOC in furrow that have undergone wet-dry cycling is more stable than SOC in berms. • Oxidation state of furrow porewater DOC is strongly suggestive of selective substrate use. • Anaerobic microbes dominate in furrow; aerobic bacteria dominate in berm. Drying-rewetting cycles are ubiquitous across natural and managed ecosystems. These cycles are known to mobilize carbon (C) in soils producing dramatic pulses in microbial respiration. While many factors contribute to these pulses, the drying-rewetting history of soils affecting carbon emissions remains unclear, especially in irrigated soils where soil moisture fluctuations are more repetitive and/or frequent than natural, seasonally influenced soils. To understand the controls of repeated wet-up and dry down effects on agricultural soils, we used a systems approach to examine the cross section of a furrow irrigated orchard to delineate soil C dynamics. Specifically, we compared two contrasting water regimes, (1) soils temporarily but repeatedly inundated during water delivery (i.e., furrows) and (2) soils at the base of trees (i.e., berms) that only receive water during precipitation events in a semi-arid Mediterranean climate. Overall, our findings show that the heterogeneous landscape of a furrow irrigated field results in two separate systems within the field scale in gaseous release of C as CO 2 , microbial selectivity of substrates, and mechanisms for C stabilization. By monitoring soil moisture as a function of depth for over two years, our results reveal that furrow soils undergo dramatic wet-dry cycles, while moisture within the berm is relatively constant. We were able to capture the distinct heterogeneity of soil moisture changes within the furrow and berm soils by continuously monitoring CO 2 flux throughout water input events in both the wet and dry season. Soil CO 2 efflux is suppressed upon irrigation within furrows, while carbon oxidation in berm soils exhibits pore-connectivity limitations that result in lower fluxes when dry. Solid phase soil C speciation determined by C 1s NEXAFS demonstrated C of higher aromaticity remained in furrow soil compared to berm soils. Microbial community analysis shows significantly different communities reside within berm and furrow soils, where furrow soils support more anaerobic metabolisms and spore-formers while berm soils have relatively higher abundance of aerobic microbes capable of degrading larger, more complex C compounds. Our findings show that water regime (periodic inundation vs episodic rainfall) controlling rewetting history can greatly differentiate C respiration within managed soils. [ABSTRACT FROM AUTHOR]

Abstract: Arsenic is contaminating the groundwater of Holocene aquifers throughout South and Southeast Asia. To examine the biogeochemical and hydrological processes influencing dissolved concentrations and transport of As within soils/sediments in the Mekong River delta, a ∼50km2 field site was established near Phnom Penh, Cambodia, where aqueous As concentrations are dangerously high and where groundwater retrieval for irrigation is minimal. Dissolved As concentrations vary spatially, ranging up to 1300μg/L in aquifer groundwater and up to 600μg/L in surficial clay pore water. Groundwaters with high As concentrations are reducing with negligible dissolved O2 and high concentrations of Fe(II), , and dissolved organic C. Within near-surface environments, these conditions are most pronounced in sediments underlying permanent wetlands, often found within oxbow channels near the Mekong River. There, labile C, co-deposited with As-bearing Fe (hydr)oxides under reducing conditions, drives the reductive mobilization (inclusive of Fe and As reduction) of As. Here, conditions are described under which As is mobilized from these sediments, and near-surface As release is linked to aquifer contamination over long time periods (100s to 1000s of years). Site biogeochemistry is coupled with extensive hydrologic measurements, and, accordingly, a comprehensive interpretation of spatial As release and transport within a calibrated hydraulic flow-field is provided of an As-contaminated aquifer that is representative of those found throughout South and Southeast Asia. [Copyright &y& Elsevier]

Wetting dry soil triggers emission of nitric oxide (NO), which can harm air quality and influence ecosystem N balance. NO released after wetting may be derived from two primary mechanisms: (1) abiotic decomposition of nitrite (NO 2 −) present in the dry soil and (2) biologically-mediated production of NO. The relative contributions of these mechanisms to NO emission are challenging to partition. To differentiate the two mechanisms, we made continuous observations of NO emission from a range of soils that varied in texture, pH, and exchangeable cations. We coupled NO gas exchange measurements with automated, non-destructive high-resolution sampling of inorganic N species via microdialysis. We identified two distinct phases of NO production (1) an initial phase that reached its maximum less than 30 min after rewetting; and (2) a second phase lasting up to 36 h. The magnitude of the initial phase of NO production was correlated with the initial nitrous acid concentration (calculated from NO 2 − concentrations and soil pH) and soil exchangeable calcium. The second phase of NO emission coincided with a peak in NO 2 − that preceded NO 3 − accumulation. Together, these results suggest that NO emissions following wetting are defined by an initial pulse of abiotic NO formation mediated by soil acidity at mineral surfaces, followed by a prolonged pulse of NO emission driven by a lag between the biological processes of ammonia oxidation and nitrite oxidation. These results can inform mechanistic models of NO emissions from soils to improve predictions of the terrestrial N cycle and atmospheric chemistry. • After wetting dry soil, nitric oxide (NO) is emitted in two distinct phases. • Chemodenitrification of NO 2 − drives NO emission immediately after wetting. • NO 2 − build up contributes to NO emission later after wetting. [ABSTRACT FROM AUTHOR]

Mining rare earth elements (REEs) can release large amounts of metal(loid)-rich dust, which can pose significant health risks to local residents. However, compared to other types of particulates, toxicity of mining dust has been largely overlooked. To provide experimental evidence on toxicity of REE mine dust, the study assessed the oxidative stress potential and genotoxicity of inhalable particles collected in a REE mining area, and associated toxicological response with source compositions. Both source types (i.e., mine and tailing area) and distances from source (i.e., industrial and residential areas) were considered when selecting the 44 sampling sites. The particle samples contained 2.3–3.5 folds higher concentrations of tested metal(loid)s than background concentrations in soil. Specially, elevated Fe, REEs, Cd, Pb were found. In spite of low cytotoxicity in lung epithelial A549 cells, there was increased cellular ROS production by of particle exposure. Samples with higher mining-originated source contributions (Provenance Index <0.3) had higher cellular ROS production (1.72 fold, 95%CI: 1.66–1.79 fold) than samples with lower mining contributions (1.58 fold, 95%CI: 1.52–1.65 fold). The factors soil (~46%), mine (~22%), and heavy metal (~20%) sources were recognized by source apportionment analysis as the main contributors to cellular ROS production; importantly, mine and heavy metal sources counted more in industrial samples. While samples generated genotoxicity, there were no differences in DNA damage between the location groups of sampling. Collectively, the results indicate that particles in mining areas may cause ROS production and DNA damage in lung cells depending on mine dust. Coupled with the long-range transportation potential of mine dust, safety measures on open pit and dust disposal sites should be adopted. Unlabelled Image • Particles around rare earth mine and tailing areas were rich in metallic components. • The particles induced cellular ROS production and genotoxicity. • Particles collected in industrial areas induced more cellular ROS than in residential areas. • Soil , mine and heavy metal sources were the main contributors to ROS. [ABSTRACT FROM AUTHOR]