长江三角洲地区人为源氨排放清单及分布特征

根据各类氨排放源的活动水平和排放因子,估算了2004年长江三角洲地区16个城市的氨排放量.结果表明,2004年长三角地区氨排放量为460.68kt,其中,氮肥使用和畜牧源是两个最大排放源,氨排放量分别为227.33kt和203.28kt,分别占长江三角洲地区氨排放总量的49.3%和44.1%,氨排放在长三角地区各城市间有较大差异,排放量超过40kt·a-1的城市为南通市、上海市、嘉兴市和泰州市,这4个城市的氨排放总量约占长三角地区氨排放量的42.5%.长江三角洲地区氨平均排放强度为4.20t·km-2·a-1,排放强度超过6t·km-2·a-1的城市为嘉兴市、南通市、泰州市和上海市,其中,嘉兴市的排放强度最大,为10.83 t·km-2·a-1.     

三江源地区生态系统生态功能分析及其价值评估

在地理信息系统的支持下,将相关地图数字化并利用已有的地形数据库等资料,研究了三江源地区生态系统土壤保持、涵养水源、固定CO2和释放O2等4项生态功能,并利用市场价值法、机会成本法和影子工程法等评估了其生态功能的价值.研究结果表明:三江源地区生态系统土壤保持总量为1.0383×109t·a-1,其价值总计为1.2528×109元·a-1;植被凋落物和土壤涵养水源能力为1.6469×1010t·a-1,涵养水源能力价值为1.1034×1010元·a-1;生态系统固定CO2为1.4128×108t·a-1,价值为1.0053×1010～4.7798×1010元·a-1;释放O2为1.0401×108t·a-1,价值为3.6709×1010～4.1605×1010元·a-1;4项生态功能合计总价值为5.9049×1010～1.0169×1011元·a-1.由此可见,三江源地区生态系统生态功能价值巨大,保护其生态系统结构和功能对我国江河中下游地区和东南亚国家生态环境安全和区域可持续发展具有重大意义.     

中国非燃煤大气汞排放量估算

本研究根据各种非燃煤大气汞排放源的活动水平和排放因子,估算了1995～2003年中国分省非燃煤大气汞的排放量。2003年中国非燃煤大气汞排放量为393t,比燃煤汞排放多137t。在非燃煤大气汞排放中,84%来自有色金属冶炼,其中锌冶炼、铅冶炼、铜冶炼和黄金冶炼分别占总排放的51%、18%、4%和11%。Hg0、Hg2+和HgP在中国非燃煤大气汞排放中所占比例分别为77%、18%和5%。中国非燃煤汞排放在各地区间有较大差异,排放量超过30t?a-1的省区包括湖南、河南和云南,排放强度超过1t?km-2的省区包括上海、湖南、河南、辽宁和广东,这些地区的主要汞排放源为有色金属冶炼和生活垃圾焚烧。1995～2003年中国非燃煤大气汞排放的年均增长率为9%,其中生活垃圾焚烧排放的年均增长率最高,达到42%。     

我国人为源CO排放量的估算研究

根据中国人为源(包括固定燃烧源、工业过程源、移动源和生物质燃烧源)的活动水平数据和相应的排放因子,对中国2000-2012年的CO排放量进行了估算。研究表明:2000-2012年,中国人为源CO排放总量呈现持续增长的趋势,年均增长率为3.53%,其中工业过程源是其主要排放源,2012年其排放量占总排放量的42%左右;固定燃烧源、工业过程源、移动源和生物质燃烧源排放的主要来源分别为工业部门、钢铁行业、道路移动源和室内秸秆燃烧;CO排放量在地区间的分布极不平衡,2012年排放量最高的5个省份依次是河北、山东、江苏、河南和辽宁;排放强度较大的地区主要集中在环渤海经济圈和长三角地区,其中又以上海、天津2个直辖市的排放强度最大。     

南通市人为源大气氨排放清单及特征

根据收集的南通市各类人为氨排放源的活动水平数据,采用合理的估算方法和排放因子,估算了2009年南通市的人为源大气氨排放量。结果表明,2009年南通市人为源大气氨排放量为60.02 kt,其中,畜禽源和氮肥使用是两个最大排放源,氨排放量分别为31.54 kt和23.43 kt,分别占南通市大气氨排放总量的52.5%和39.0%。畜禽源中生猪是NH3排放最大贡献源,占畜禽源排放总量的46.4%,其次是家禽,其贡献率为36.4%。南通市氨平均排放强度为6.59 t.km-2.a-1。     

南通市人为源大气氨排放清单及特征

根据收集的南通市各类人为氨排放源的活动水平数据,采用合理的估算方法和排放因子,估算了2009年南通市的人为源大气氨排放量。结果表明,2009年南通市人为源大气氨排放量为60.02 kt,其中,畜禽源和氮肥使用是两个最大排放源,氨排放量分别为31.54 kt和23.43 kt,分别占南通市大气氨排放总量的52.5%和39.0%。畜禽源中生猪是NH3排放最大贡献源,占畜禽源排放总量的46.4%,其次是家禽,其贡献率为36.4%。南通市氨平均排放强度为6.59 t.km-2.a-1。     

中国生物质燃烧大气污染物排放清单

根据2000-2007年各省市生物质燃烧消耗量和排放因子,估算了中国大陆生物质燃烧所导致的NOx、SO2、CO、CO2、CH4、NMHC、PM、BC排放量,并给出了分省区、分生物质类型的排放清单.研究表明,2007年中国生物质燃烧排放的NOx、SO2、CO、CO2、CH4、NMHC、PM和BC排放量分别为109万t,1...     

中国水泥工业CO2排放现状及减排对策

水泥工业是中国制造业中温室气体CO2的主要排放源,因此,根据水泥生产的基本原理和工艺特点,建立了CO2排放的数学模型并确定排放强度,计算了2001—2010年中国水泥工业CO2的排放量,分析了影响CO2排放量的主要因素及其发展趋势,并提出水泥工业CO2减排对策.结果表明,中国水泥工业CO2排放总量逐年增长,与水泥产量和单位产品原料、燃料消耗定额呈线性关系;在CO2排放总量中,原料煅烧和燃料燃烧阶段的排放量分别占49%和51%;"十一五"期间单位水泥产品CO2排放强度由0.69t.t-1下降到0.65t.t-1.万元GDPCO2排放量呈下降趋势,2008年达到最低值为0.3054t,平均每年万元GDPCO2排放量下降10.69%,说明水泥工业10年间实施节能降耗、资源循环利用、提高经济效益等措施对于减少CO2排放具有明显效果.     

红河州人为源氨排放清单及分布特征

根据收集的红河州各类人为源氨排放活动水平数据和排放因子,建立了2017年红河州人为源氨分类别和县市排放清单。结果表明,2017年红河州人为氨源排放总量为93. 21kt,其中农田生态系统、畜牧养殖业和其它源排放量分别为10. 43kt、71. 18kt和11. 6kt,畜牧养殖业是红河州氨排放的主要来源,占排放总量的73. 37%。弥勒市、建水县和泸西县是红河州氨排放量最大的3个县市,排放量为36. 57kt,排放份额占红河州总排放量的39. 23%,排放量最小的是河口县为0. 85kt,仅占全州的0. 91%。红河州的氨排放强度为3. 0t/km2·a-1,泸西县是氨排放强度最大县市,高达6. 8t/km2·a-1。     

长江经济带湖北省人为源VOCs排放清单及变化特征

以人为源挥发性有机物（VOCs）为研究对象,以5类源活动水平数据为基础,采用排放因子法建立了长江经济带湖北省2018年人为源VOCs排放清单,并进一步研究了2009~2018期间工艺过程源VOCs排放特征及变化趋势.结果表明,湖北省2018年人为源VOCs排放总量为6.52×10⁵ t,约占全国总排放量的6.41%;化石燃料固定燃烧源、工艺过程源、溶剂使用源、移动源和废弃物处理源对湖北省的贡献分别为3.26%、76.39%、4.54%、14.72%和1.09%.涉及9个行业45个子类的工艺过程源在VOCs排放中占比突出,其中武汉市和宜昌市的VOCs排放量较高.从经济水平和区域面积分别分析了各市州工艺过程源VOCs排放强度,天门市和神农架林区单位GDP的VOCs排放量较高,而武汉市、鄂州市和天门市单位面积VOCs排放量较高.2009年VOCs排放量从2.45×10⁵ t逐年递增,2015~2017年趋于稳定,最大排放量达7.01×10⁵ t,2018年VOCs排放量降至4.98×10⁵ t,与全国人为源VOCs排放趋势相同.化学原料及化学制品制造业、橡胶和塑料制造业是其变化的主要驱动力,10年间贡献分别为33.85%~51.55%和7.07%~38.13%.其中化学药品原药、化学农药原药生产在10年间对VOCs排放贡献占据重要优势,而泡沫塑料生产排放量变化大,在2015~2017年突增到2.00×10⁴ t以上.湖北省在国家及地方相关政策引导下,重点行业VOCs减排效果显著.     

Effects of two sludge application on fractionation and phytotoxicity of zinc and copper in the soil

The potential harm of heavy metals is a primary concern in application of sludge to the agricultural land. A pot experiment was conducted to evaluate the effect of two sludges on fractionation of Zn and Cu in soil and their phytotoxicity to pakchoi. The loamy soil was mixed with 0%, 20%, 40%, 60% and 80% (by weight) of digested sewage sludge (SS) and composted sludge (SC). The additions of both sludges caused a significant raise in all fractions, resulting in that exchangeable (EXCH) and organic bound (OM) became predominance of Zn and organic bound Cu occupied the largest portion. There was more available amount of Zn and Cu in SS treatments than SC treatments. During the pot experiment, the concentration of Zn in EXCH, carbonate (CAR) and OM and Cu in EXCH and OM fractions decreased in all treatments, so their bioavailability reduced. Germination rate and plant biomass decreased when the addition rate was high and the best yield appeared in 20% mixtures at the harvest of pakchoi. The two sludges increased tissue contents of Zn and Cu especially in the SS treatments. Zn in pakchoi was not only in relationship to ΔEXCH and ΔCAR forms but also in ΔOM forms in the sludge-soil mixtures. Tissue content of Cu in pakchoi grown on SC-soils could not be predicted by ΔEXCH. These correlation rates between Zn and Cu accumulation in pakchoi and variation of different fractions increased with time, which might indicate that sludges represented stronger impacts on the plant in long-term land application.     

Intraspecific differences in effects of co-contamination of cadmium and

A hydroponic experiment was carried out to study intraspecific differences in the effects of different concentrations of cadmium (Cd)(0-10 mg/L) and arsenate (As(V)) (0-8 mg/L) on the growth parameters and accumulation of Cd and As in six wheat varieties Jing-9428, Duokang-1, Jingdong-11, Jing-411, Jingdong-8 and Zhongmai-8. The endpoints of wheat seedlings, including seed germination,biomass, root length and shoot height, decreased with increasing the Cd and As concentrations. Significant differences in seed germination, biomass, root length, shoot height and the accumulation of Cd and As were observed between the treatments and among the varieties (p ＜ 0.05). The lethal dosage 50% were about 20, 80, 60, 60, 80 and 20 mg As/L for Jing-9428, Duokang-1, Jingdong-11,Jing-411, Jingdong-8 and Zhongmai-8, respectively, and the corresponding values for Cd were about 30, 80, 20, 40, 60 and 10 mg Cd/L, respectively. Among the six varieties, Duokang-1 was found to be the most resistant to Cd and As toxicity, and Zhongmai-8 was the most sensitive to Cd and As co-contamination. The resistance of the six varieties was found dependant on the seedling uptake of Cd and As. Duokang-1 was the most suitable for cultivation in Cd and As co-contaminated soils.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.