内蒙古河套灌区地下水矿化度的时空变异特征

利用内蒙古河套灌区义长灌域地下水水位、水质资料（1996-2005）,结合地理信息系统（G IS）技术,运用传统统计学和地统计学方法研究灌域10年间地下水矿化度时空变异性。结果表明：1.灌域内地下水矿化度在1996-2005年间呈下降趋势（从1996年的8.5 g/L下降到2005年的约5.3 g/L）,且变异系数不大;2.地下水矿化度的变化受降水、蒸发、地下水位和引黄水量等多种因素的影响,蒸发与地下水矿化度达到极显著相关;3.1996年和2005年两个时期的地下水矿化度的实际变异函数和理论变异函数（球状模型）拟合较好,F检验达到显著水平。Kriging差值结果显示,两个时期矿化度的空间分布差异不甚明显。     

黄河口典型潮滩湿地土壤净氮矿化与硝化作用

采用PVC顶盖埋管原位培育法研究了黄河口典型潮滩湿地土壤净氮矿化与净硝化作用的动态变化特征、影响因素及净氮矿化/硝化量.结果表明,高潮滩湿地(LW)、中潮滩湿地(JP1)和低潮滩湿地(JP2)0~15cm土壤无机氮含量具有明显的季节变化特征,NH4+-N含量表现为LW＞JP1＞JP2,NO3--N含量则表现为JP1＞LW＞JP2.3种湿地土壤净氮矿化/硝化速率均呈明显的波动变化.生长季的净氮矿化量分别为27.81、11.90和0.33kg/hm2,净硝化量分别为12.09、15.99和1.19kg/hm2,净硝化量占净氮矿化量的百分比分别为43.47%、100.00%和100.00%.相关分析表明,湿地土壤净氮矿化量与土壤水分含量呈显著负相关,而土壤净氮硝化量与土壤pH值呈显著负相关.3种潮滩湿地土壤在维持无机氮方面的能力整体表现为LW＞JP1＞JP2,说明从氮循环角度高潮滩湿地系统最为稳定,而低潮滩湿地系统的稳定性最差.     

The degradation of anilazine and dihydroxy‐anilazine at various soil depths of an orthic luvisol

Abstract

In conformity with Guideline 4.1 of the Federal German Biological Agency, degradation experiments with the fungicide active ingredient [benzene ring‐U‐¹⁴C]anilazine and its major metabolite [triazine ring‐U‐¹⁴C]dihydroxy‐anilazine were carried out in an orthic luvisol. Mineralization of the benzene ring carbon of anilazine amounted to less than 2 % in 110 days and that of the triazine ring carbon of dihydroxy‐anilazine to less than 8 %. Increasing the incubation temperature from 22 °C to 30 °C and adding organic substance influenced the mineralization slightly. In soils which received two or three applications in succeeding years with subsequent ageing in the open‐air lysimeter no stimulation of the mineralization was observed. Extractions after incubation showed that only 10.2 to 18.6 % of the ¹⁴C‐activity applied with anilazine was extractable with acetone/CaCl₂. The major proportion was bound in the fractions of the soil organic matter, namely 45.0 to 59.6 % of the radiocarbon applied was accounted for by the humin fraction, 12.0 to 27.4 % by the fulvic acids, and 9.4 to 15.0 % by the humic acids. In the case of dihydroxy‐anilazine, 28.9 to 89.7 % of the applied ¹⁴C‐activity was extractable with acetone/CaCl₂. Of tJhe radiocarbon bound in the soil, the greatest proportion, i.e. 18.5 to 35.5 % of the radiocarbon applied, was accounted for by the fulvic acids.     

3,5-二硝基苯甲酸降解菌A3的分离及降解特性

 从硝基苯类化合物废水处理系统中分离到一株3,5-二硝基苯甲酸降解菌株A3,经形态特征、生理生化以及16S rDNA序列分析,初步鉴定为睾丸酮丛毛单胞菌(Comamonas testosteroni).该菌能以200mg/L3,5-二硝基苯甲酸为唯一碳源,12h的降解率可达95%以上,24h可溶性有机碳(DOC)由72.5mg/L降至10.2mg/L,表明3,5-二硝基苯甲酸被降解矿化而不是被转化成其他有机物.当A3以200mg/L3,5-二硝基苯甲酸为唯一碳、氮源时,将底物转化为一种黄色代谢产物,该产物不易进一步降解.A3降解3,5-二硝基苯甲酸的适宜温度为20～30℃,最适pH值为5～9.     

微生物诱导碳酸盐沉淀及其在固定重金属领域的应用进展

生物矿化已受到化学、物理、生物、材料、医学、生命及环境等多学科的广泛关注,其中,以尿素为底物的MICP（微生物诱导碳酸盐沉淀）技术是生物矿化领域的研究热点之一.在分析MICP过程中的酶解机理和生物大分子在微生物矿化过程中的作用基础上,通过对重金属离子的矿化产物和碳酸盐矿化菌的成矿因素分析,揭示MICP矿化产物的特征及形成条件.碳酸盐矿化菌主要产生脲酶分解尿素,增加土壤CO₃2-饱和度,其代谢产生的胞外聚合物具有多种功能团组合和键能连接,起着调控生物矿化的作用.MICP技术可用于固定土壤和水体中的Cu、Pb、Zn、Cd、Cr、As等重金属,重金属主要以共沉淀的形式被固定,阴阳离子型重金属以类质同象置换方式分别占据方解石中的CO₃2-位和Ca2+位,从而促使污染土壤中的可交换态重金属向碳酸盐结合态转移.但是,MICP技术主要针对减少重金属的生物可利用性,不能满足以全量来计算的现行土壤环境质量标准,且MICP技术在长期有效性、生物安全性和土壤理化性质等方面存在诸多隐患.因此,由试验条件转向实际应用具有一定挑战.建议寻找更稳定的方法以阻止碳酸盐矿物中的重金属溶出,且有必要将开发高效的土著微生物复合菌剂作为未来MICP研究的方向之一.      

铋银氧化物混合物高效氧化降解四溴双酚A的研究

以Ag NO3和Na Bi O3·2H2O为原料,采用离子交换-共沉淀法制备了铋银氧化物混合物(silver bismuth oxide,BSO),并利用它氧化降解溴代阻燃剂四溴双酚A(TBBPA).研究了制备过程中银铋摩尔比及降解过程中BSO用量对TBBPA降解效果的影响.结果表明,当银铋摩尔比为1∶1,BSO用量为1 g·L-1时,40 mg·L-1TBBPA在7 min内可完全降解,其总有机碳的去除率高达80%.采用离子色谱、气相色谱-质谱联用仪及X射线光电子能谱监测降解过程中TBBPA的变化,发现TBBPA降解过程涉及脱溴、叔丁基碳的断裂和苯环的开环氧化等反应.利用Na N3作为分子探针,发现单线态氧是BSO氧化降解TBBPA的主要反应活性物种.     

生物炭对滨海湿地盐碱土壤碳氮循环的影响

滨海湿地盐碱土壤在全球碳氮循环及调节气候变化中起着重要作用。环境友好型土壤改良剂生物炭（Biochar,BC）在缓解气候变化和促进农业可持续发展方面前景巨大。然而,现有研究多关注BC对滨海湿地盐碱土壤中温室气体排放及土壤氮素流失的影响,缺乏其对滨海湿地盐碱土壤碳氮循环的深入研究和系统总结。本文综合分析了施用BC对滨海湿地盐碱土壤植被碳库、有机碳库、有机碳矿化及生物固氮、硝化、反硝化、矿化、氨损失等碳氮循环过程的影响和可能机制。指出未来应关注长期野外研究,利用宏基因组等现代分子生物技术,阐明BC对土壤碳氮循环影响的分子生物学机制,以期为滨海湿地生态系统的修复与功能保育提供理论依据。     

Fate of the veterinary antibiotic 14C-difloxacin in soil including simultaneous amendment of pig manure with the focus on non-extractable residues

The fate of ¹⁴C-labeled difloxacin (¹⁴C-DIF) was studied in time course experiments after application on soil (Ap horizon of silt loam) and amendment of authentic DIF containing pig manure (146 mL kg^?1; 4.17 MBq kg^?1; 0.85 mg kg^?1) or water (124 mL kg^?1; 0.42 MBq kg^?1; 0.09 mg kg^?1) for 56 and 120 days of incubation, respectively.

Mineralization of ¹⁴C-DIF was below 0.2% in both experiments after 56 days or 120 days. In the course of the experiments, portions of extractable radioactivity (Accelerated Solvent Extraction (ASE); acetonitrile-water) decreased to 19–21% depending only little on manure amendment. Non-extractable residues of ¹⁴C-DIF increased to 70–74% after 56 days and 120 days, respectively, and therefore were the main route of ¹⁴C-DIF in soil. According to radioanalytical HPLC and LC-MS/MS, only the parent compound was found in all extracts over the whole time of the experiment. According to fractionation of the non-extractable residues (NER) into particle size fractions, ¹⁴C portions were associated to the water used for fractionation, the silt and clay fractions, whereas no radioactivity was detected in the sand fraction. The majority of ¹⁴C was found within the clay fractions.

Fractionation of humic components showed that radioactivity derived from ¹⁴C-DIF was associated with humic acids, fulvic acids, humins and minerals and very little with soluble, non-humic HCl fraction. The highest portions of radioactivity were found in the fulvic acid fraction. Results obtained by size exclusion chromatography (SEC) of the purified fulvic acids were similar for every sample analyzed. One large portion of ¹⁴C co-eluted with fulvic acids of a molecular weight below 910 g mol^?1. Both fractionation methods demonstrated that the parent compound DIF or initial metabolites were rapidly integrated into humic materials and, thus, were major components of NER.     

季节性温度升高对落干期消落带土壤氮矿化影响

为揭示季节性温度升高对消落带落干期土壤氮矿化的影响,分别采集三峡支流澎溪河消落带上游和下游两个水文断面,155 m(低)、165 m(中)和175 m(高)这3个水位高程表层土壤,结合落干期气温变化特点,在25℃和35℃两个温度下进行恒温培养.结果表明,消落带土壤总氮和硝态氮在上游断面和高水位高程含量更高,而下游和低水位高程含量更低,铵态氮分布与其相反.硝态氮是无机氮的主要存在形式,占无机氮的57.4%~84.7%.相同培养温度下,氨化、硝化、净氮矿化速率均表现为随水位高程增加,随流域断面由下至上而显著增加(P0.05);总体上,在水位高程和流域断面上均表现为:温度升高使硝化速率和净氮矿化速率显著增加(P0.05),而对土壤氨化速率无显著影响(P0.05).     

The fate of nitrogen in a moderately alkaline and calcareous soil amended with biosolids and urea

The determination of nitrogen (N) based loading rates for land application of biosolids is challenging and site specific. Over loading may contribute to environmental, agricultural, or human health problems. The objective of this study was to monitor N mineralization and losses in a moderately alkaline and calcareous desert soil amended with either anaerobically digested (AN) or lime-stabilized (LS) biosolids, and irrigated with and without urea enriched water. For Experiment 1, N inputs, leaching and residuals in soil were evaluated in an open soil column system. For Experiment 2, ammonia (NH₃) emissions were evaluated in a closed soil column system. In Experiment 1, AN and LS biosolids increased soil ON (organic N) by three and two fold, respectively. Respective net N mineralization of ON from biosolids alone was 90% and 62% without urea, and 71% and 77%, respectively with added urea. Nitrogen leaching losses and residuals in amended soil did not account for all N inputs into the soil/biosolids system. In Experiment 2, NH₃ emissions were not significantly different among treated soils with or without added urea, except LS amended soil receiving urea. Ammonia losses did not account for unaccounted N in Experiment 1. We concluded that deep placement and rapid mineralization of AN biosolids promoted anaerobic soil conditions and denitrification, in addition to the high denitrification potential of desert soil. LS biosolids showed greater potential than AN biosolids for safe and beneficial land application to desert soils regardless of biosolids placement and the inclusion of N rich irrigation water.