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Urban activity emissions have important ecological significance to bacterial communities' spatial and temporal distribution and the mechanism of bacterial community construction. The mechanism of bacterial community construction is the key to community structure and lifestyle, and the influence of this aspect has not been thoroughly studied. This study analyzed the response of bacteria in water and sediment in different seasons to urban activities in Jinsha River. The results showed that the influence of urban activities on bacterial community structure in sediment was greater than that in water. The input of pollution in different regions changed the diversity and abundance of water and sediments bacteria and promoted bacterial community reconstruction to a certain extent. Co-network analysis found that many metal-mediated species are core species within the same module and can be used to mitigate pollution caused by metal or organic pollutants due to interspecific solid interactions. Different potential pollution sources around urban rivers affect the metabolic function of bacteria in aquatic ecosystems and promote the detoxification function of bacteria in different media. The results of this study supplement our understanding of the characteristics of microbial communities in urban river systems and provide clues for understanding the maintenance mechanism of microbial diversity in multi-pollution environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Isotope technology is an ideal tool for tracing the sources of certain pollutants or providing insights into environmental processes. In recent years, the advent of multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) has enabled the precise measurement of various metal stable isotopes. Due to the presence of "fingerprint" properties in various environmental samples, metal stable isotopes have been applied to distinguish the source of contaminants effectively and further understand the corresponding environmental processes. The environmental fate of metal elements is strongly controlled by adsorption, an essential process for the distribution of elements between the dissolved and particulate phases. The adsorption of metal elements on mineral and organic surfaces significantly affects their biogeochemical cycles in the environment. Therefore, it is crucial to elucidate the fractionation characteristics of stable metal isotopes during the adsorption process. In this review, three typical transitional metal elements were selected, considering Mo as the representative of anionic species and Fe and Zn as the representative of cationic species. For Mo, the heavier Mo isotope is preferentially adsorbed in the solution phase, pH has a more significant influence on isotope fractionation, and temperature and ionic strength are relatively insensitive. Differences in coordination environments between dissolved and adsorbed Mo during adsorption, i.e., attachment mode (inner- or outer-sphere) or molecular symmetry (e.g., coordination number and magnitude of distortion), are likely responsible for isotopic fractionation. For Fe, The study of equilibrium/kinetic Fe isotopic fractionation in aqueous Fe(II)-mineral is not simple. The interaction between aqueous Fe(II) and Fe (hydroxyl) oxides is complex and dynamic. The isotope effect is due to coupled electron and atom exchange between adsorbed Fe(II), aqueous Fe(II), and reactive Fe(III) on the surface of Fe (hydroxyl) oxide. For Zn, the heavier Fe isotope preferentially adsorbs on the solid phase, and pH and ionic strength are essential influencing factors. The difference in coordination environment may be the cause of isotope fractionation., Competing Interests: Declaration of Competing Interest We declare that we have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)

In this study, the core carcinogenic elements in Xuanwei Formation coal were identified. Thirty-one samples were collected based on the age-standardized mortality rate (ASMR) of lung cancer; Si, V, Cr, Co, Ni, As, Mo, Cd, Sb, Pb, and rare earth elements and yttrium (REYs) were analyzed and compared; multivariate statistical analyses (CA, PCA, and FDA) were performed; and comprehensive identification was carried out by combining multivariate statistical analyses with toxicology and mineralogy. The final results indicated that (1) the high-concentration Si, Ni, V, Cr, Co, and Cd in coal may have some potential carcinogenic risk. (2) The concentrations of Cr, Ni, As, Mo, Cd, and Pb meet the zoning characteristics of the ASMR, while the Si concentration is not completely consistent. (3) The REY distribution pattern in Longtan Formation coal is lower than that in Xuanwei Formation coal, indicating that the materials of these elements in coal are different. (5) The heatmap divides the sampling sites into two clusters and subtypes in accordance with carcinogenic zoning based on the ASMR. (6) PC1, PC2, and PC3 explain 62.629% of the total variance, identifying Co, Ni, As, Cd, Mo, Cr, and V. (7) Fisher discriminant analysis identifies Ni, Si, Cd, As, and Co based on the discriminant function. (8) Comprehensive identification reveals that Ni is the primary carcinogenic element, followed by Co, Cd, and Si in combination with toxicology. (9) The paragenesis of Si (nanoquartz), Ni, Co, and Cd is an interesting finding. In other words, carcinogenic elements Ni, Co, Cd, and Si and their paragenetic properties should receive more attention., (© 2024. The Author(s).)

The study on the origin of quartz and silica in Xuanwei Formation coal in Northwest Yunnan, China, is helpful to understand the relationship between quartz and silica and the high incidence of lung cancer from the root. To address these questions, the mineralogy and microscopic studies of silica in Xuanwei Formation coal were performed. The following results were obtained: (1) silica in the late Permian Xuanwei Formation coal seams originated from detrital input, early diagenesis, and late diagenesis. (2) A more significant contribution comes from early diagenesis, which contains abundant authigenic quartz and amorphous silica. (3) Quartz and silica from inorganic silicon are more symbiotic with kaolinite and from biogenic silicon with chamosite. (4) Three silica polymorphs in coal samples have been identified: opal-A (amorphous silica), opal-CT/-C (cristobalite/tridymite), and α quartz. (5) Opal-A is ubiquitous, while opal-CT/-C and α quartz are rare. (5) Opal-A is an amorphous and nontoxic ordinary silica. (6) Since the toxicity of amorphous silica and its presence in coal is an emerging topic, it should be continuously monitored., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Metal mineral mining results in releases of large amounts of heavy metals into the environment, and it is necessary to better understand the response of rhizosphere microbial communities to simultaneous stress from multiple heavy metals (HMs), which directly impacts plant growth and human health. In this study, by adding different concentrations of cadmium (Cd) to a soil with high background concentrations of vanadium (V) and chromium (Cr), the growth of maize during the jointing stage was explored under limiting conditions. High-throughput sequencing was used to explore the response and survival strategies of rhizosphere soil microbial communities to complex HM stress. The results showed that complex HMs inhibited the growth of maize at the jointing stage, and the diversity and abundance of maize rhizosphere soil microorganisms were significantly different at different metal enrichment levels. In addition, according to the different stress levels, the maize rhizosphere attracted many tolerant colonizing bacteria, and cooccurrence network analysis showed that these bacteria interacted very closely. The effects of residual heavy metals on beneficial microorganisms (such as Xanthomonas, Sphingomonas, and lysozyme) were significantly stronger than those of bioavailable metals and soil physical and chemical properties. PICRUSt analysis revealed that the different forms of V and Cd had significantly greater effects on microbial metabolic pathways than all forms of Cr. Cr mainly affected the two major metabolic pathways: microbial cell growth and division and environmental information transmission. In addition, significant differences in rhizosphere microbial metabolism under different concentrations were found, and this can serve as a reference for subsequent metagenomic analysis. This study is helpful for exploring the threshold for the growth of crops in toxic HM soils in mining areas and achieving further biological remediation., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Haze pollution has been a public health issue. The skin microbiota, as a component of the first line of defense, is disturbed by environmental pollutants, which may have an impact on human health. A total of 74 skin samples from healthy students were collected during haze and nonhaze days in spring and winter. Significant differences of skin fungal community composition between haze and nonhaze days were observed in female and male samples in spring and male samples in winter based on unweighted UniFrac distance analysis. Phylogenetic diversity whole-tree indices and observed features were significantly increased during haze days in male samples in winter compared to nonhaze days, but no significant difference was observed in other groups. Dothideomycetes, Capnodiales, Mycosphaerellaceae, etc. were significantly enriched during nonhaze days, whereas Trichocomaceae, Talaromyces , and Pezizaceae were significantly enriched during haze days. Thus, five Talaromyces strains were isolated, and an in vitro culture experiment revealed that the growth of representative Talaromyces strains was increased at high concentrations of particulate matter, confirming the sequencing results. Furthermore, during haze days, the fungal community assembly was better fitted to a niche-based assembly model than during nonhaze days. Talaromyces enriched during haze days deviated from the neutral assembly process. Our findings provided a comprehensive characterization of the skin fungal community during haze and nonhaze days and elucidated novel insights into how haze exposure influences the skin fungal community. IMPORTANCE Skin fungi play an important role in human health. Particulate matter (PM), the main haze pollutant, has been a public environmental threat. However, few studies have assessed the effects of air pollutants on skin fungi. Here, haze exposure influenced the diversity and composition of the skin fungal community. In an in vitro experiment, a high concentration of PM promoted the growth of Talaromyces strains. The fungal community assembly is better fitted to a niche-based assembly model during haze days. We anticipate that this study may provide new insights on the role of haze exposure disturbing the skin fungal community. It lays the groundwork for further clarifying the association between the changes of the skin fungal community and adverse health outcomes. Our study is the first to report the changes in the skin fungal community during haze and nonhaze days, which expands the understanding of the relationship between haze and skin fungi., Competing Interests: The authors declare no conflict of interest.

The oxidation/weathering of molybdenite (MoS 2 ) is too slow to be monitored, even under pure oxygen and high temperatures, while it proceeds rapidly through humid air. The adsorption of water molecules on molybdenite is necessary for the wet oxidation/weathering of molybdenite. Therefore, we employ kinetic Monte Carlo modeling to clarify the adsorption isotherm, site preferences and kinetics of water on different surfaces of molybdenite. Our results indicate that (1) the adsorption capacity and adsorption rate coefficient of H 2 O on the (110) surface are significantly larger than those on the (001) surface at a temperature of 0~100 °C and a relative humidity of 0~100%, suggesting that the (110) surface is the predominant surface controlling the reactivity and solubility of molybdenite in its interaction with water; (2) the kinetic Monte Carlo modeling considering the adsorption/desorption rate of H 2 O, dissociation/formation rate of H 2 O and adsorption/desorption of dissociated H indicates that the adsorption and dissociation of H 2 O on the (110) surface can be completed in one microsecond (ms) at 298 K and in wet conditions; (3) the adsorption and dissociation of H 2 O on molybdenite are not the rate-limiting steps in the wet oxidation/weathering of molybdenite; and (4) kinetic Monte Carlo modeling explains the experimental SIMS observation that H 2 O and OH (rather than H + /H - or H 2 O) occupy the surface of MoS 2 in a short time. This study provides new molecular-scale insights to aid in our understanding of the oxidation/weathering mechanism of molybdenite as the predominant mineral containing molybdenum in the Earth's crust.

Isolating relevant microorganisms is still a substantial challenge that limits the use of bacteria in the maintenance of human health. To confirm which media and which bacterial colony densities can enrich certain kinds of bacteria, we selected eight common media and used them to enrich the gut microorganisms on agar plates. Then, we calculated the numbers of bacterial colonies and collected the bacterial culture mixtures from each kind of medium. Using the Illumina HiSeq platform, we analyzed the composition and diversity of the culture-enriched gut bacterial community. Our data suggested that medium supplemented with blood could increase the diversity of the bacterial community. In addition, beef powder and peptone could significantly change the culture-enriched bacterial community. A moderate density (100-150 colony-forming units per plate) was optimal for obtaining the highest diversity on the agar. Similarly, membrane transport was significantly enriched in the moderate-density group, which indicated a more active metabolism in this density range. Overall, these results reveal the optimal culture conditions, including the densities of colonies and nutritional components for various gut bacteria, that provide a novel strategy for isolating bacteria in a way that is targeted and avoids blinded and repetitive work.

We attempt to understand the pollution characteristics and carcinogenic risk of toxic elements around Hutou Village, Xuanwei City, Yunnan Province, China. For this propose, 48 road dust samples were collected systematically, and the concentrations of Cr, Ni, Cu, Zn, As, Cd, Pb, Co, and Cr(IV) were analyzed and compared; the spatial distribution was obtained. The I geo and EF indices and multivariate statistical analysis (CA, PCA, HACA) were carried out for source investigation, and human health risk assessment was also adopted to evaluate local non-carcinogenic and carcinogenic risks. The result showed that Cr, Ni, Cu, Cd and Co contaminations were quite serious; Zn, As, Cd, and Pb had similar distribution pattern, and Cr and Ni also shared similar distribution characteristics; Cd, Pb, Zn, and As ascribed to anthropogenic sources, while Cr and Ni originated from either anthropogenic activity or natural sources; Co and Cu originated from natural sources; the non-carcinogenic risk of Co cannot be ignored. The carcinogenic risk of Ni was considered unacceptable. Finally, an indoor coal-burning pattern was established that the high Cd and Ni inhalation and ingestion model was associated with lung cancer.

Chengdu, a megacity in southwestern China, experiences severe air pollution; however, knowledge of the seasonal variation in mass concentration, extent of potentially harmful elements (PHEs) contamination, and sources caused by heavy metals remains lacking. This study adopted a weighting method to calculate the daily mass concentration of PM 1 and used ICP-MS to determine PHE concentrations. Results indicated that PM 1 mass concentration was in the range 5.44-105.91 μg/m 3 . Seasonal PM 1 mass concentration could be arranged in the following order: winter > fall > spring > summer. The concentrations of PHEs in the PM 1 sample mostly showed the same seasonal variation characteristics as mass concentration. The average concentration of each PHE decreased as follows: Cu (107.44) > Zn (81.52) > Pb (22.04) > As (8.17) > Sb (1.91) > Ni (1.87) > Cr(VI) (0.84) > Cd (0.40) > Tl (0.33) (ng/m 3 ). Enrichment factor values varied markedly from mild to anomalous enrichment. Principal component analysis revealed mainly derived from the fossil fuel combustion (55.215%).

This paper systematically studied the mass concentration levels of PM 2.5 and PM 10 and obtained the morphological characteristics and components of the particles through scanning electron microscopy (SEM-EDX) and discussed the sources of the particles. Meanwhile, the health risk was evaluated according to the mass concentration of particulate matter. The results showed that the average annual PM 2.5 and PM 10 in the eastern part of Chengdu were 101.99 μg/m 3 and 168.89 μg/m 3 , respectively, exceeding the national second-level average annual air quality standard (GB3095-2012). Both of them were the highest in winter and the lowest in summer and had a significant positive correlation. The atmospheric particles in the study area were mainly composed of fly ash particles, soot aggregates, mineral particles (sulfate mineral particles, carbonate mineral particles, etc.), which mainly came from coal burning, dust, automobile exhaust and secondary products. The results of the health risk assessment showed that the mass concentration of PM 2.5 and PM 10 in the atmosphere of the eastern part of Chengdu exceeded the IT-1 target. The average annual air quality index was 185.84, and the air quality index was level 4, classified as medium pollution. PM 10 and PM 2.5 were both excessive pollutants, and PM 10 was the primary pollutant. Relevant measures should be taken to control particulate matter sources to some extent.

Concentrations of Pb and Cd in topsoil from 24 locations along the Baguan River near a smelting dump in west Panzhihua were measured using ICP-MS to examine the spatial distributions of these toxic heavy metals. Twenty-one profile samples, 7 from each of 3 locations down to 80 cm, were also analyzed to establish background levels and Pb - Cd correlations. Lead isotopic ratios in all 45 samples and potential sources of soil contamination were determined using MC-ICP-MS. Contamination levels of Pb and Cd in soils from both sides of the river ranged from low to moderate, and the concentrations of Pb and Cd exhibited highly correlated behavior. Results of an isotope-tracer technique determined the number of end-member contaminants and background compositions contributing to the compositions of topsoils. Results of a binary mixing model indicated that contaminants in upslope soils from relatively higher elevations were coal and derivative products, and that these soils are isotopically distinct from downslope soils. Contaminants in downslope soils were slag and derivative products from V processing. Results demonstrate the use of Pb isotopic tracers in low-to-moderate contaminant levels to predict potential sources and Pb is a viable surrogate to trace potential Cd contamination in Panzhihua region., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Photochemical vapor generation (PVG) has emerged as a promising sample introduction method for atomic spectrometry in recent years. Despite its great success, a major impediment for the wide application of PVG is the interferences from the coexisting ions, especially transition-metal ions. In this work, iron and 1,3,5-benzenetricarboxylic (Fe-BTC), a Fe-containing metal-organic framework (MOF) material, was synthesized and first used as a platform integrating the sample matrix separation, preconcentration, and photocatalysis for the highly selective determination of elements by PVG. Bismuth was selected as a model analyte. Fe-BTC served not only as the photocatalyst for the PVG of Bi 3+ but also as an efficient absorbent for the separation of analytes from the sample matrix. Compared with the previous PVG system, the performance of tolerating interferences toward coexisting ions of the proposed method has been greatly improved after using Fe-BTC-based matrix separation. Thus the excess of 10 mg L -1 of Co 2+ and 100 mg L -1 of Cu 2+ , Ni 2+ , and Fe 3+ caused no obvious interferences for 1 μg L -1 of Bi determination. Under the optimal conditions, the limit of detection (LOD, 3σ) of the developed method was 0.3 ng L -1 with the inductively coupled plasma-mass spectrometry (ICPMS) measurement, which could be lowered down to 0.04 ng L -1 after ten times of preconcentration with Fe-BTC prior to analysis. This method was successfully applied for the analysis of Bi in complicated sample matrices of soil (GBW07401), sediment (GBW07310), nickel-iron alloy (GBW01622), and nickel alloys (GBW01641) by the external calibration method.

An enhanced photochemical vapor generation (PVG) sample introduction procedure is developed for the determination of trace Bi with inductively coupled plasma mass spectrometry (ICP MS) by the addition of iron. Gas chromatography mass spectrometry (GC-MS) reveals that (CH 3 ) 3 Bi is the major component of the volatile Bi species formed in the presence of 20% (v/v) acetic acid, 5% (v/v) formic acid, and 60 μg mL -1 Fe 3+ under UV irradiation. The addition of Fe 3+ not only largely increases the PVG efficiency of Bi 3+ but also accelerates the reaction kinetics of photochemical reduction of Bi 3+ . The analytical sensitivity was enhanced 30-fold using PVG for sample introduction compared to that for direct solution nebulization detection by ICP MS detection. Furthermore, the proposed method shows much better tolerance of interference from Cu 2+ and Ni 2+ than that from conventional hydride generation (HG). Under the optimized conditions, a detection limit of 0.3 ng L -1 was obtained for Bi by ICP MS determination. The relative standard deviation (RSD) was 2.5% for seven replicate measurements of 0.5 ng mL -1 Bi 3+ standard solution. The proposed method has been successfully applied for the determination of Bi in environmental samples, including water samples, and certified reference material of soil (GSS-1) and sediments (GSD-5a and GSD-10) with satisfying results.

In this study, 2LFh was synthesized, and the effects of 2LFh synthesis in the laboratory as well as its synthetic products' mineral crystal phase changes during high temperature aging process caused by Ca 2+ , Mg 2+ , and Cl - were also studied. In addition, the Cd 2+ adsorption effects of the products above with different pH values and different Cd 2+ concentrations were studied in this experiment. The results showed that the existence of Ca 2+ had no significant effect on the synthesis and aging of 2LFh. However, in the presence of Mg 2+ and Cl - , the akaganeite could be found in the synthetic material, and with the increase of the ion concentration, the crystallinity of the formed akaganeite was higher. And akaganeite had a significant inhibitory effect on the aging of 2LFh, causing the Cd 2+ adsorption effect of 2LFh after aging was better than that of pure 2LFh. The adsorption and removal rates of Cd 2+ in Fh2 series and Fh2-200 series were increased with the increase of initial concentration. With the increase of pH, the adsorption capacity and removal rate were increased, and the removal rate reached nearly 100% when pH value is ranging from 10 to 11. The isothermal adsorption experiment showed that the isothermal adsorption process of Cd 2+ in Fh2 series and Fh2-200 series was in accordance with the Freundlich model. The affinity coefficient (Kf) of the Freundlich model of Fh2-200 series arranged in descending order is Fh2-200-Mgs> Fh2-200-Cas> Fh2-200s, showing that the Cd 2+ adsorption capacity of Fh2-200 was relatively weak, while that of Fh2-200-Ca series and Fh2-200-Mg series was relatively strong, which was confirmed by the experimental results.

Photochemical vapor generation (PVG) is emerging as a promising analytical tool for Te determination, thanks to its efficient matrix separation, and simple and green procedure. However, the low PVG generation efficiency of Te is the bottleneck for its wide application in environmental samples containing trace Te. Herein, we reported a high efficient PVG for Te determination by synergistic effect of ferric ion and nano-TiO 2 . The analytical sensitivity was enhanced approximately 15-fold for Te(IV) in the presence of both ferric ions and nano-TiO 2 , comparing to conventional PVG. Besides, the use of nano-TiO 2 can provide Te(VI) and Te(IV) an equal and high PVG efficiency in the presence of ferric ions, owned to the high photocatalytic performance of TiO 2 under short-wavelength UV irradiation (254 and 185 nm). Under the optimized experimental conditions, a detection limit of 1.0 ng L -1 was obtained. The precision of replicate measurements was 2.3% (RSD, n = 7) at 0.5 μg L -1 for Te(IV). The methodology was validated by successful determination of Te in surface waters and two standard reference sediment samples. To our best knowledge, this is the first report of the synergistic enhancement of transitional metal ions and nano-TiO 2 in PVG, which possesses potential for highly sensitive determination of vapor-forming elements.

High-precision measurement of X-ray spectra is affected by the statistical fluctuation of the X-ray beam under low-counting-rate conditions. It is also limited by counting loss resulting from the dead-time of the system and pile-up pulse effects, especially in a high-counting-rate environment. In this paper a detection system based on a FAST-SDD detector and a new kind of unit impulse pulse-shaping method is presented, for counting-loss correction in X-ray spectroscopy. The unit impulse pulse-shaping method is evolved by inverse deviation of the pulse from a reset-type preamplifier and a C-R shaper. It is applied to obtain the true incoming rate of the system based on a general fast-slow channel processing model. The pulses in the fast channel are shaped to unit impulse pulse shape which possesses small width and no undershoot. The counting rate in the fast channel is corrected by evaluating the dead-time of the fast channel before it is used to correct the counting loss in the slow channel.

Ambient PM 10 air samples were collected at two industrial sites and one urban residential site in the mining city of Panzhihua, China, from April, 2014, to January, 2015. Mass concentrations of ten trace metals (As, Cd, Cr, Ni, Co, V, Mn, Cu, Pb, and Zn) in PM 10 were determined by inductively coupled plasma-mass spectrometry. The results showed Zn, Pb, Cu, Mn and V were the most abundant elements from the industrial sites. Concentrations for Cd, Cr, Co, Ni, Mn and Cu at industrial sites greatly exceeded the air quality standards of the World Health Organization and the Chinese Ministry of Environmental Protection. Principal component analysis indicated that the main sources of the trace metals were steel smelting, fuel combustion, geological and mineral dust. Four different clusters of particles (i.e., mineral, calcium-containing, soot and aluminosilicate) were identified by scanning electron microscopy coupled with energy dispersive X-ray spectrometry. Chromium (Cr) was found to present the highest excess cancer risk, implying the potential for carcinogenic health effects in local inhabitants. Manganese (Mn) presented a non-carcinogenic health risk to children and adults, while the other metals were within acceptable limits.

The effects of rhizodeposition on soil C and N availabilities lead to substantial changes of microbial community composition and processes in the rhizosphere of plants. Under heterogeneous light, photosynthates can be translocated or shared between exposed and shaded ramets by clonal integration. Clonal integration may enhance the rhizodeposition of the shaded ramets, which further influences nutrient recycling in their rhizosphere. To test the hypothesis, we conducted a pot experiment by the stoloniferous herb Glechoma longituba subjected to heterogeneous light. Microbial biomass and community composition in the rhizosphere of shaded offspring ramets, assessed by phospholipid fatty acids (PLFAs) analysis, were markedly altered by clonal integration. Clonal integration positively affected C, N availabilities, invertase and urease activities, N mineralization (Nmin) and nitrification rates (Nnitri) in the rhizosphere of shaded offspring ramets. However, an opposite pattern was also observed in phenoloxidase (POXase) and peroxidase (PODase) activities. Our results demonstrated that clonal integration facilitated N assimilation and uptake in the rhizosphere of shaded offspring ramets. The experiment provides insights into the mechanism of nutrient recycling mediated by clonal integration.