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941.
Soils from two typical tidal salt marshes with varied salinity in the Yellow River Delta wetland were analysed to determine possible effects of salinity on soil carbon sequestration through changes in soil microbiology. The mean soil respiration (SR) of the salt water–fresh water mixing zone (MZ) was 2.89 times higher than that of the coastal zone (CZ) (4.73 and 1.63?μmol?m?2?s?1, respectively, p?.05), and soil dehydrogenase activity was the main microbial factor influencing SR. In addition to the higher soil microbial biomass, the MZ had more β-Proteobacteria than the CZ, as well as some specific bacteria with strong heterotrophic metabolic activity such as Pseudomonas sp. and Limnobacter sp. that might have led to its higher dehydrogenase activity and respiratory rates. Additionally, the CZ possessed more Halobacteria and Thaumarchaeota with the ability to fix CO2 than the MZ. Significantly lower soil salinity in MZ (4.25?g?kg?1) was suitable for β-Proteobacteria, but detrimental for Halobacteria compared with CZ (7.09?g?kg?1, p?.01), which might lead to the lower microbial decomposition capacity of soils in CZ. As a result, the CZ has a higher soil organic carbon content than the MZ. 相似文献
942.
943.
944.
Perfluorinated compounds in the Pearl River and Yangtze River of China 总被引:27,自引:0,他引:27
So MK Miyake Y Yeung WY Ho YM Taniyasu S Rostkowski P Yamashita N Zhou BS Shi XJ Wang JX Giesy JP Yu H Lam PK 《Chemosphere》2007,68(11):2085-2095
A total of 14 perfluorinated compounds (PFCs) were quantified in river water samples collected from tributaries of the Pearl River (Guangzhou Province, south China) and the Yangtze River (central China). Among the PFCs analyzed, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were the two compounds with the highest concentrations. PFOS concentrations ranged from 0.90 to 99 ng/l and <0.01–14 ng/l in samples from the Pearl River and Yangtze River, respectively; whereas those for PFOA ranged from 0.85 to 13 ng/l and 2.0–260 ng/l. Lower concentrations were measured for perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctanesulfoamide (PFOSA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorononaoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA). Concentrations of several perfluorocarboxylic acids, including perfluorododecanoic acid (PFDoDA), perfluorotetradecanoic acid (PFTeDA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctadecanoic acid (PFOcDA) were lower than the limits of quantification in all the samples analyzed. The highest concentrations of most PFCs were observed in water samples from the Yangtze River near Shanghai, the major industrial and financial centre in China. In addition, sampling locations in the lower reaches of the Yangtze River with a reduced flow rate might serve as a final sink for contaminants from the upstream river runoffs. Generally, PFOS was the dominant PFC found in samples from the Pearl River, while PFOA was the predominant PFC in water from the Yangtze River. Specifically, a considerable amount of PFBS (22.9–26.1% of total PFC analyzed) was measured in water collected near Nanjing, which indicates the presence of potential sources of PFBS in this part of China. Completely different PFC composition profiles were observed for samples from the Pearl River and the Yangtze River. This indicates the presence of dissimilar sources in these two regions. 相似文献
945.
Loos R Gawlik BM Locoro G Rimaviciute E Contini S Bidoglio G 《Environmental pollution (Barking, Essex : 1987)》2009,157(2):561-568
This study provides the first EU-wide reconnaissance of the occurrence of polar organic persistent pollutants in European river waters. More than 100 individual water samples from over 100 European rivers from 27 European Countries were analysed for 35 selected compounds, comprising pharmaceuticals, pesticides, PFOS, PFOA, benzotriazoles, hormones, and endocrine disrupters. Around 40 laboratories participated in this sampling exercise. The most frequently and at the highest concentration levels detected compounds were benzotriazole, caffeine, carbamazepine, tolyltriazole, and nonylphenoxy acetic acid (NPE1C). Only about 10% of the river water samples analysed could be classified as “very clean” in terms of chemical pollution. The rivers responsible for the major aqueous emissions of PFOS and PFOA from the European Continent could be identified. For the target compounds chosen, we are proposing “indicative warning levels” in surface waters, which are (for most compounds) close to the 90th percentile of all water samples analysed. 相似文献
946.
Occurrence, sources, and inventory of hexabromocyclododecanes (HBCDs) in soils from Chongming Island, the Yangtze River Delta (YRD) 总被引:6,自引:0,他引:6
Hexabromocyclododecanes (HBCDs) is a concern due to their large usage combining with physico-chemical properties and toxicity to wildlife and human. However, very limited data were reported on HBCDs in soils, especially from rural area. In this study, 22 soil samples were collected from Chongming Island at estuary of the Yangtze River Delta, to investigate the level, diasteroisomer profile, potential sources, and mass inventory of HBCDs. The total concentrations ranged from not detected to 93.8 pg g−1 dry weight (dw) with a mean of 23.3 pg g−1 dw, which was at the low end of the global levels. The wide distribution of HBCDs in soils suggested that the local emissions of HBCD-containing materials and/or the inputs via atmospheric transport from other regions were two possible sources. Variation of HBCDs levels was observed in different types of soils. Woodland, tideland and road soils contained slightly higher HBCDs than those of farmland and grassland. Overall, γ-HBCD was the dominant diasteroisomer in soils, followed by α-HBCD and β-HBCD. Significant but weak correlations were only found between α-HBCD and β-HBCD versus TOC content in soils. Currently, the mass inventory of HBCDs in soils of Chongming Island was 5.3 kg. Based on these data, we gave perspective on human intake of HBCDs via soil ingestion by age. Local resident’s intakes ranged from 15.5 to 97.8 fg kg body weight−1 d−1, in which children are exposed more than adults. 相似文献
947.
九龙江污染物入海通量初步估算 总被引:9,自引:0,他引:9
河流污染物入海通量的研究是研究海水污染的内容之一。本文对目前常用的河流污染物通量估算方法进行了分析,根据九龙江的水文水质监测数据,选择高锰酸钾指数与NH3-N作为代表性水质监测项目,利用各种估算公式进行污染物入海通量估算,对估算结果进行比较发现部分公式适用性较好。估算结果表明,2003年九龙江污染物入海通量CODMn大约为21 000 t/a,NH3-N大约为2 500 t/a。根据与其他研究结果的对比,探讨了河流污染物入海通量估算的特点,对不足之处作了说明。 相似文献
948.
介绍了国外流域水环境监测现状,分析了我国流域水环境监测发展概况,提出了金沙江中游流域水环境监测体系建立的必要性,论述了金沙江中游流域水环境监测体系初步构建的设计原则、监测点布设、监测因子筛选、监测系统建设、共享信息平台建设等。 相似文献
949.
赣江流域土地利用方式对无机氮的影响 总被引:5,自引:2,他引:5
赣江无机氮是鄱阳湖氮素输入的主要来源,查明流域土地利用方式对赣江无机氮的影响对鄱阳湖的富营养化防治具有重要意义.基于2013年1月和6月对赣江干流和主要支流NO-3-N和NH+4-N的浓度测定,通过不同空间尺度和土地类型等级划分,利用相关分析和冗余分析研究土地利用方式对赣江无机氮浓度的影响.结果表明,不同空间尺度的子流域划分方式对赣江流域土地利用类型与无机氮浓度的相关性有较大影响.与NO-3-N相比,选择更小的子流域划分尺度有助于分析土地利用方式对NH+4-N浓度的影响;在温度较高、微生物活动强烈的季节,也应选择更小的子流域划分尺度研究土地利用方式对无机氮浓度的影响.一级土地利用分类下,赣江流域水田、水域对NO-3-N起"源"作用,林地、草地起"汇"作用;居民建设用地对NH+4-N起"源"作用,林地起"汇"作用.二级土地利用分类下,水田中丘陵水田是赣江NO-3-N浓度的主要来源,其次为平原水田,山区水田最小.居民建设用地中的城镇用地和其它工矿建设用地是赣江NH+4-N的主要污染来源,农村用地是NO-3-N的主要污染来源. 相似文献
950.
延河流域降雨侵蚀力时空分布特征 总被引:10,自引:1,他引:10
降雨侵蚀力(R)反映了降水引起土壤水蚀的潜在能力,其时空分布规律定量研究是进行土壤侵蚀预报的基础.利用延河流域22个雨量站24a逐日降雨资料,分析了该区降雨侵蚀力的时空分布特征.结果表明,降雨侵蚀力与降雨量、侵蚀性降雨量具有一致的年内年际变化趋势.降雨侵蚀力年内变化为单峰型,集中分布在5~9月,占全年R值的91.61%.降雨侵蚀力多年平均值为1580.58MJ.mm.(hm2.h.a)-1,最高值(1981年)为2417.70MJ.mm.(hm2.h.a)-1,最低值(1999年)仅585.29MJ.mm.(hm2.h.a)-1,年际间变化为中等变异,变异系数为0.32.烧房砭站多年平均R值最大,为2190.33MJ.mm.(hm2.h.a)-1,镰刀湾和杨山站多年平均R值最小,分别为1151.37MJ.mm.(hm2.h.a)-1和1146.87MJ.mm.(hm2.h.a)-1.R值与侵蚀性降雨量具有一致的空间分布格局,北部雨量站R值年际变化呈现轻微的增加趋势,其它站点R值年际变化相对呈现出轻微的减少趋势,总体上延河流域降雨侵蚀力呈现下降趋势,趋势系数为-0.004. 相似文献