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22821. 题目: Changes in soil organic carbon and total nitrogen in apple orchards in different climate regions on the Loess Plateau The Loess Plateau is the largest high-quality apple-producing area in China. However, the responses of soil organic carbon (SOC) and total nitrogen (TN) concentrations and stocks to long-term cultivation in apple orchards under different climate regions remain unclear. We conducted soil sampling in apple orchards distributed throughout the main apple-production area on the Loess Plateau. A total of 28 soil samples (max depth 500 cm) from stands of different ages at 7 soil sampling sites were collected to evaluate the changes in SOC and TN concentrations and stocks; furthermore, C:N ratios across apple orchards in different climate regions were evaluated. Compared with those in the semihumid region, SOC concentration and stock in the 0–500 cm soil profile were 6.6% and 32.1% lower, respectively, in the semiarid region. Furthermore, over the entire soil profile, TN concentration and stock were 12.1% and 38.4% lower, respectively, in the semiarid region than in the semihumid region. However, the C:N ratios in the semiarid region were higher than those in the semihumid region. SOC and TN concentrations generally decreased with increasing soil depth, and those in the 0–120 cm soil layer were significantly higher than those at the other soil depths in both climate regions. The most important factors, which control the variability of SOC and TN, were precipitation, plantation age, topographical properties (altitude and landform of apple orchards) and soil type. These results not only provide information on the effects of changes in SOC and TN concentrations and stocks and C:N ratios but also provide regional-level information that can aid the sustainable development of apple orchards on the Loess Plateau. | |||||
22822. 题目: Boron speciation and extractability in temperate and tropical soils: a multi-surface modeling approach Boron is an essential micronutrient for plants, but can also be toxic when present in excess in the soil solution. A multi-surface geochemical model was used to assess the important processes that affect the distribution of the geochemically reactive B in soils over the solution and solid phase. The multi-surface model was based on the adsorption of B on dissolved and solid humic acids, representing reactive organic matter, ferrihydrite, representing the Fe and Al (hydr)oxides, and clay mineral edges. In addition, the performance of previously proposed extraction methods for measuring reactive B was evaluated. Based on B measured in 0.01 M CaCl2 soil extracts (7-85 μmol kg-1 soil), we calculated the reactive boron concentration for 5 temperate and 5 tropical soils (8-106 μmol kg-1 soil). We found that extractions with 0.43 M HNO3 or with 0.2 M mannitol + 0.1 M triethanolamine buffer extract on average 240 and 177 % of the reactive B predicted by the model, thus releasing additional B that is assumed to be not or only very slowly available for exchange with the soil solution. Reactive B calculated by the model corresponded best to the B measured in a 0.05 M KH2PO4 (pH 4.5) extraction. In general, the multi-surface modeling showed that 68 % or more of reactive boron was present in the solution phase for the soils in this study and that the adsorption was dominated by oxides in the tropical soils, while solid organic matter was the main adsorbent in the temperate soils. When changing the soil pH(CaCl2), B concentration was found to decrease with increasing pH, and both experimental data and modelling suggests that this effect is mainly due to increased binding of B to organic matter. | |||||
22823. 题目: V V Reduction by Polaromonas spp. in Vanadium Mine Tailings | |||||
22824. 题目: Converting alfalfa pasture into annual cropland achieved high productivity and kept soil organic carbon in a semiarid area Converting alfalfa (Medicago sativa L.) into cropland (rotated cropland, RC) is a common way of land use to reuse degraded alfalfa pasture. However, it is a big challenge for RC to achieve high productivity and maintain high soil organic carbon (SOC) achieved by previous alfalfa. We converted a long‐term alfalfa pasture into RC in 2010, and study the effects of fertilization on soil moisture, crop productivity, and SOC in RC and continuous cropland (CC), both under plastic film mulching, from 2010 to 2018. Before the conversion, alfalfa pasture had higher SOC (12.3%) and total N (7.7%) compared to CC. However, it not only occurred severe soil desiccation, but the available P and inorganic‐N were only about 39.4% and 25.1% of CC. After the conversion, soil moisture in RC at 0‐0.6 m restored up to CC only after one year, and restored to 95.3% and 69.2% of CC at 0.6‐2 and 2‐5 m throughout nine‐years. Crop yield and biomass in RC with fertilization were not significant to CC since the third year due to the increased available P and inorganic‐N, and sufficient soil moisture restoration at 0‐0.6 m. SOC in RC without fertilization decreased by 8.1% throughout nine‐years, while RC with fertilization consistently kept SOC up with previous alfalfa due to the increased biomass, inorganic‐N, and total N. These findings help to eliminate concerns about the continuously low production and rapid decline of SOC in croplands converted from alfalfa and support for sustainable high‐productivity and high SOC sequestration in dryland farming. This article is protected by copyright. All rights reserved. | |||||
22825. 题目: Enhanced adsorption of tetracycline by an iron and manganese oxides loaded biochar: Kinetics, mechanism and column adsorption A Fe/Mn oxides loaded biochar (FeMn-BC) was prepared to enhance the adsorption of tetracycline (TC). γ-Fe2O3 and MnO2 were assigned to the Fe and Mn oxides, respectively. The enhanced adsorption of TC was dominated by the loaded γ-Fe2O3 and MnO2. According to Akaike-Information-Criteria evaluation, Elovich kinetic and Langmuir isotherm models could best describe the adsorption with a maximum capacity of 14.24 mg/g. During adsorption process, the γ-Fe2O3 and MnO2 hydrolyzed into hydroxides (FeOOH and MnOOH) which acted as bases to complex with TC2− ion under alkaline condition (pH = 11). After the adsorption, the concentrations of leached Fe and Mn could meet the requirements PRC standards GB13456-2012 and GB8978-1996, respectively. The FeMn-BC had ~24% on TC removal (initial concentration of 20 mg/L) after four-cycles regeneration. The FeMn-BC was also available for TC adsorptions in column tests and actual wastewater. | |||||
22826. 题目: Reviews and syntheses: The mechanisms underlying carbon storage in soil | |||||
22827. 题目: Complex interactions of in-stream DOM and nutrient spiralling unravelled by Bayesian regression analysis | |||||
22828. 题目: Significant increase of assimilable organic carbon (AOC) levels in MBR effluents followed by coagulation, ozonation and combined treatments: Implications for biostability control of reclaimed water | |||||
22829. 题目: Formation of carbonaceous and nitrogenous iodinated disinfection byproducts from biofilm extracellular polymeric substances by the oxidation of iodide-containing waters with lead dioxide Lead dioxide (PbO2) is an important form of lead mineral scales in drinking water pipes. Iodide (I−) widely presents in source waters and can be thermodynamically oxidized by PbO2 to the reactive iodine species (I2/HOI). Biofilm extracellular polymeric substances (EPS) are nonnegligible precursors of disinfection byproducts (DBPs). The aim was to study the oxidation of I− by PbO2 and formation of iodinated DBPs (I-DBPs) from EPS. At a high molar ratio of PbO2 to I− (> 100), the observed rate constants of I− oxidation decreased as pH increased from 6.0 to 9.0 with an H+ dependence of 0.79, and the rate constant (k) was 1.6 × 1011 M−2.79 s−1. Most of formed I2/HOI (> 92%) was transformed to organic iodine in the presence of EPS. EPS had a lower formation potential (FP) of carbonaceous I-DBPs (C-IDBPs), while a higher that of nitrogenous I-DBPs (N-IDBPs) than HA, resulting in a higher Chinese Hamster Ovary cell cytotoxicity. Generally, the formation of I-DBPs decreased with the increase of pH due to the reduction of surface positive charge and electrochemical driving force. PbO2 dose and I− concentration also had a significant effect on the I-DBPs formation. EPS proteins had a higher FP of both C- and N-IDBPs than polysaccharides on account of more electrophilic sites and higher nitrogen content. In proteins, aspartic acid was the main contributor to triiodomethane and iodoacetic acids formation, whereas aspartic acid, asparagine and tyrosine were the major precursors of diiodoacetonitrile and diiodoacetamide. The study helps to improve the control strategy of I-DBPs when biofilm outbreaks in lead-containing water pipes. | |||||
22830. 题目: Characterising organic carbon sources in Anthropocene
affected Arctic upland lake catchments, Disko Island, West
Greenland | |||||
22831. 题目: Microbial inputs at the litter layer translate climate into altered organic matter properties Plant litter chemistry is altered during decomposition but it remains unknown if these alterations, and thus the composition of residual litter, will change in response to climate. Selective microbial mineralization of litter components and the accumulation of microbial necromass can drive litter compositional change, but the extent to which these mechanisms respond to climate remains poorly understood. We addressed this knowledge gap by studying needle litter decomposition along a boreal forest climate transect. Specifically, we investigated how the composition and/or metabolism of the decomposer community varies with climate, and if that variation is associated with distinct modifications of litter chemistry during decomposition. We analyzed the composition of microbial phospholipid fatty acids (PLFA) in the litter layer and measured natural abundance δ13CPLFA values as an integrated measure of microbial metabolisms. Changes in litter chemistry and δ13C values were measured in litterbag experiments conducted at each transect site. A warmer climate was associated with higher litter nitrogen concentrations as well as altered microbial community structure (lower fungi:bacteria ratios) and microbial metabolism (higher δ13CPLFA). Litter in warmer transect regions accumulated less aliphatic‐C (lipids, waxes) and retained more O‐alkyl‐C (carbohydrates), consistent with enhanced 13C‐enrichment in residual litter, than in colder regions. These results suggest that chemical changes during litter decomposition will change with climate, driven primarily by indirect climate effects (e.g. greater nitrogen availability and decreased fungi:bacteria ratios) rather than direct temperature effects. A positive correlation between microbial biomass δ13C values and 13C‐enrichment during decomposition suggests that change in litter chemistry is driven more by distinct microbial necromass inputs than differences in the selective removal of litter components. Our study highlights the role that microbial inputs during early litter decomposition can play in shaping surface litter contribution to soil organic matter as it responds to climate warming effects such as greater nitrogen availability. | |||||
22832. 题目: Cutting oil-water emulsion wastewater treatment by microwave assisted catalytic wet peroxide oxidation Cutting-oil in water emulsions (COWE) suppose an environmental threat due to their high volume, stability and low biodegradability (BOD5/COD: 0.07). So far, these effluents have been treated by physical methods which merely transfer the pollutants into another phase. In this work, Microwave-assisted Catalytic Wet Peroxide Oxidation (MW-CWPO) is used for the first time in the degradation of COWE 0.5%w, using graphite as catalyst. Working at pH0: 9, graphite: 10 g/L, 15.7 g/L H2O2, at MW power of 800 W by pulsation method, complete demulsification and 82% Total Organic Carbon (TOC) removal is achieved in only 10 min. Furthermore, the remaining TOC in solution is mainly ascribed to malonic, acetic and formic acids, which results in readily biodegradable effluents (BOD5/COD: 0.93). The degradation mechanism is a complex combination of H2O2-mediated adsorption of the pollutants onto the graphite's surface and its subsequent oxidation mediated by hot-spots induced by MW radiation. This work also studies the influence of pH0, catalyst load and H2O2 dosage in COWE degradation. Finally, catalyst stability upon 3 consecutive cycles was tested and various techniques are proposed and examined for catalyst regeneration. | |||||
22833. 题目: Biomarker constraints on Mediterranean climate and ecosystem transitions during the Early-Middle Miocene Paleoenvironmental and paleoclimatic variations experienced by the Mediterranean region during the mid-Miocene Burdigalian-Langhian interval have been investigated through analysis of biomarker signals (n-alkanes and glycerol dialkyl glycerol tetraethers, GDGTs) from slope mudstones of the northern Apennines (Marne di Vicchio Fm). Terrestrial signatures in marine sediments reflected by preserved long-chain n-alkanes with a identifiable odd-over-even carbon number predominance attest to the thermal immaturity of the sedimentary rock. Abundances of n-C27, n-C29 and n-C31 alkanes, coupled with the carbon isotopic signatures of the n-C31 homologue suggest that Mediterranean vegetation crossed a transition phase adapting to arid conditions that may favored a shift from woodland to wooded grassland during the Middle Miocene. This ecosystem evolution could have been favored by the passage from warm humid conditions to a warm drier climate, as indicated by GDGT-based TEX86 and BIT indexes. Strong similarities between these Mediterranean biomarker records and those from the Atlantic (DSDP Sites 94, 516, 608) imply a constant connection of the western Mediterranean to the Atlantic Ocean from ~19 Ma to ~14.5 Ma. | |||||
22834. 题目: Making the Biotic Ligand Model kinetic, easier to develop, and more flexible for deriving water quality criteria In aquatic environments, the ecological risks posed by metals are greatly affected by water chemistry, thereby creating challenges for water quality management. Biotic ligand models (BLMs) have become the most widely used tools to interpret and predict water chemistry effects. Traditional BLM development methods require a large number of toxicity tests and organisms, and model predictions are limited to certain toxicity statistics (e.g., 48-h median effective concentration, 48-h EC50), to which the models were calibrated. To address these limitations, we propose a new method to develop BLMs by integrating them into the toxicokinetic-toxicodynamic (TK-TD) framework. Metal bioaccumulation was predicted from metal exposure and water chemistry using the BLM-type toxicokinetics, whilst metal toxicity was predicted from metal bioaccumulation using the toxicodynamics. Using the new method, we developed a kinetic BLM of cadmium for Daphnia magna with only six toxicity tests and 1540 daphnids; this represents a 60−80% reduction compared to the traditional methods. The model was validated in the presence of commercial dissolved organic matter (DOM) and in natural waters sampled from 12 lakes. The kinetic BLM was able to accurately simulate the protective effects of the commercial DOM by employing the Stockholm humic model, whilst the complexation capabilities of some natural DOM were overestimated. We further used the model to predict Cd EC50 and no-effect concentrations for different waters, generating predictions close to the effect concentrations reported in the literature. Overall, our method requires fewer resources and presents an easier approach to develop BLMs; the kinetic BLM is more flexible and can serve as a useful tool for developing water quality criteria. | |||||
22835. 题目: Let more big fish sink: Fisheries prevent blue carbon sequestration--half in unprofitable areas | |||||
22836. 题目: The effects of temperature on soil phosphorus availability and phosphatase enzyme activities: a cross-ecosystem study from the tropics to the Arctic | |||||
22837. 题目: The Bioavailability Of Dissolved, Particulate, And Adsorbed Organic Carbon In Groundwater Systems Dissolved organic carbon (DOC) is the smallest amount of organic carbon present in aquifer systems and is typically dwarfed by amounts of particulate organic carbon (POC) and adsorbed organic carbon (AOC). Research conducted over the last half century, however, has shown that these dissolved, particulate, and adsorbed compartments interact dynamically with each other. That suggests the hypothesis that the bioavailability of DOC in groundwater may indicate the bioavailability of the associated POC and AOC compartments as well. If that proves to be the case, it would greatly simplify the process of evaluating the bioavailability of total organic carbon present in groundwater systems. That hypothesis was examined by (1) comparing DOC bioavailability between two aquifers receiving modern atmospheric recharge, but with the recharge passing through POC/AOC sources of substantially different geologic ages, and (2) measuring POC/AOC bioavailability in sediments in from two aquifers before and after injection with bioavailable DOC consisting of dissolved sugars and emulsified vegetable oil. The results of both comparisons are consistent with the hypothesis that DOC bioavailability in groundwater reflects the bioavailability of the associated POC and AOC compartments and vice versa. Thus, DOC bioavailability may be a useful indicator of an aquifer's potential to drive reduction/oxidation processes that affect the chemical quality of groundwater. This article is protected by copyright. All rights reserved. | |||||
22838. 题目: Engineering porous biochar for capacitive fluorine removal Chronic accumulation of fluoride (F−) threats human health and eventually brings about skeletal fluorosis, dental fluorosis and joint deformation, which has aroused global attention. As an emerging technique, electrosorption presented great potential in wastewater purification. The key role in electrosorption is the exploitation of economical, environmentally-friendly and efficient electrode material. Nowadays, many existing investigations on the preparation of porous carbon material focused on the introduction of extra dopant and activation reagent. However, the information concerning the preparation of pure porous biochar and the inherent environmental significance is neglected. Here, a win–win strategy, named conversion waste biomass into porous biochar, has been applied in capacitive fluorine removal. The results indicated that the capacity of porous biochar electrode was 1.28 mg/g, which was improved by 48.8% in contrast to activated carbon electrode. Furthermore, competition experiments revealed concentration-dependence interference in the present of foreign ions. Electrosorption cycle experiment manifested excellent stability of the biochar electrodes. The electrode was regenerated without consuming any chemicals and could produce current for energy recovery. More importantly, continuous-flow experiment showed that the removal efficiency of F− was 91.98% at the synthetic wastewater. High specific capacitance, low internal resistance and appropriate pore distribution were responsible for the F− removal mechanism. Overall, this work would pioneer a facile method in the preparation of low-price electrode material and their potential applications in environmental remediation. | |||||
22839. 题目: Combined effects of rice straw-derived biochar and water management on transformation of chromium and its uptake by rice in contaminated soils Chromium (Cr) pollution in soil is a global problem owing to its wide industrial use. The mobility, toxicity, and crop uptake of Cr depends on its valence state. Cr(VI) is highly mobile and toxic whereas Cr(III) is generally considered immobile and less toxic. We performed a pot experiment to investigate the combined effects of rice straw-derived biochar and water management on transformation of Cr and its uptake by rice in contaminated soils. The main plots had water management treatments of alternating wetting and drying (AWD) and continuous flooding (CF), and the subplots had three levels of straw biochar (0, 5, and 10 g kg−1). The results showed that water management and the addition of biochar had a significant effect on the dynamics of soil redox potential (Eh), pH, dissolved organic carbon (DOC), and Fe(II) concentration. As these parameters are important factors affecting Cr transformation in paddy soils, the dynamics of the Cr(III) and Cr(VI) concentrations were clearly different under different treatments. The highest reduction of Cr(VI) was observed in the treatment with CF water management in combination with 10 g kg−1 of biochar amendment, which resulted in a 62% reduction of Cr(VI) to Cr(III) in soil. The alterations in the oxidation state of Cr greatly affected its accumulation in the rice grains. The CF combined with 10 g kg−1 of biochar treatment, caused the Cr concentration in rice grains to be 66.2% lower compared with that of the unamended control under AWD water management. Possibly owing to the reduction in phytotoxic effects of Cr(VI), the combined treatment showed an improvement in rice grain weight. In conclusion, the combination of 10 g kg−1 of biochar amendment and CF water management may potentially be used in Cr-contaminated soil to mitigate the impacts of Cr contamination on rice production. | |||||
22840. 题目: Nanoscale zerovalent iron, carbon nanotubes and biochar facilitated the phytoremediation of cadmium contaminated sediments by changing cadmium fractions, sediments properties and bacterial community structure Environment functional materials have been widely used, but whether their effects on the contaminated environment could facilitate phytoremediation is not yet well understood. In this study, starch stabilized nanoscale zerovalent iron (SN), multiwall carbon nanotubes (MW) and tea waste derived biochar (TB) were used to facilitate the phytoremediation of cadmium (Cd) contaminated sediments by Boehmeria nivea (L.) Gaudich. Results showed that 100 mg/kg SN, 500 mg/kg MW and 500 mg/kg TB facilitated phytoremediation, as evidenced by increasing Cd accumulation and/or promoting plant growth. These concentrations of materials increased the reducible fraction of Cd by 9–10% and decreased the oxidizable proportion of Cd by 48–52%, indicating the improvement of Cd bioavailability through converting the oxidizable Cd into reducible form. The activities of urease, phosphatase and catalase, which related to nutrient utilization and oxidative stress alleviation, increased by 20–24%, 25–26%, and 8–9% in the sediments treated with 500 mg/kg MW and 500 mg/kg TB, respectively. In addition, the 16S rRNA gene sequence results showed that these concentrations of materials changed the bacterial diversity. The abundance of Acidobacteria, Actinobacteria, Nitrospirae and Firmicutes were increased by some of the applied materials, which could promote plant growth, change Cd bioavailability and reduce Cd toxicity. These findings indicated that the applied environment functional materials could facilitate the phytoremediation of Cd contaminated environment by changing Cd fractions, sediments properties and bacterial community structure. | |||||