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51.
中国主要红树林湿地中甲基汞的分布特征及影响因素初探 总被引:4,自引:2,他引:2
通过对海南、广东、广西、福建的8个主要红树林地区沉积物中甲基汞以及环境因子的研究,分析了红树林生态系统中甲基汞的分布及其汞的甲基化作用.结果表明:①沉积物中总汞和甲基汞的含量分布并不一致.中国主要红树林区海南(三亚、东寨港)、广东(特呈岛、雷州、高桥、福田)、广西(大冠沙)、福建(浮宫)表层沉积物中甲基汞含量分别为(0.24±0.04)、(0.58±0.27)、(0.52±0.23)、(1.56±0.49)、(0.50±0.25)、(1.21±0.36)、(1.86±1.04)和(0.47±0.16)ng.g-1.甲基汞含量有很明显的地域区别,其含量顺序为大冠沙雷州福田东寨港特呈岛高桥浮宫三亚.工业和养殖业输入的汞和有机质显著增加了沉积物中甲基汞水平.对比世界其他河口湿地,我国红树林湿地沉积物中的甲基汞污染较为严重.②红树林沉积物的甲基化比率介于0.11%~7.13%.甲基化比率顺序由大到小为大冠沙特呈岛雷州福田高桥东寨港三亚浮宫.甲基化比率与砂粒显著正相关(p0.05),与粉粒和黏粒显著负相关(p0.05).③沉积物中总细菌含量范围为2.44×1010~1.91×1011CFU/g(以干重计,下同),浮宫三亚高桥东寨福田大冠沙.各环境因子对微生物数量的影响无显著差异.沉积物中SRB的含量介于1.73×104~4.92×106CFU/g,福田浮宫东寨港三亚高桥大冠沙.高有机废水是导致沉积物中SRB含量增高的主要原因.沉积物类型对SRB在沉积物表层的分布也有较大影响.甲基汞和环境因子之间并没有明显的相关性,外源输入是我国红树林湿地沉积物中的甲基汞污染的主要原因. 相似文献
52.
Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental
problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and
sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated
runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters
the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg
contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of
higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The
concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4
2??) were lower during higher flow due to dilution. Due to both sedimentation
of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within
10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60%
for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction
(DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved
phase in surface waters in Wanshan (over 95%). 相似文献
53.
The Hg0 vapor adsorption experimental results on a novel sorbent obtained by impregnating a commercially available activated
carbon (Darco G60 from BDH) with silver nitrate were reported. The study was performed by using a fundamental approach, in an
apparatus at laboratory scale in which a synthetic flue gas, formed by Hg0 vapors in a nitrogen gas stream, at a given temperature
and mercury concentration, was flowed through a fixed bed of adsorbent material. Breakthrough curves and adsorption isotherms were
obtained for bed temperatures of 90, 120 and 150°C and for Hg0 concentrations in the gas varying in the range of 0.8–5.0 mg/m3. The
experimental gas-solid equilibrium data were used to evaluate the Langmuir parameters and the heat of adsorption. The experimental
results showed that silver impregnated carbon was very effective to capture elemental mercury and the amount of mercury adsorbed by
the carbon decreased as the bed temperature increased. In addition, to evaluate the possibility of adsorbent recovery, desorption was
also studied. Desorption runs showed that both the adsorbing material and the mercury could be easily recovered, since at the end of
desorption the residue on solid was almost negligible. The material balance on mercury and the constitutive equations of the adsorption
phenomenon were integrated, leading to the evaluation of only one kinetic parameter which fits well both the experimentally determined
breakthrough and desorption curves. 相似文献
54.
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56.
An organo-montmorillonite-supported nanoscale zero-valent iron material(M-NZVI) was synthesized to degrade decabromodiphenyl ether(BDE-209). The results showed that nanoscale zero-valent iron had good dispersion on organo-montmorillonite and was present as a core-shell structure with a particle size range of nanoscale iron between 30–90 nm, characterized by XRD, SEM, TEM, XRF, ICP-AES, and XPS. The results of the degradation of BDE-209 by M-NZVI showed that the efficiency of M-NZVI in removing BDE-209 was much higher than that of NZVI. The efficiency of M-NZVI in removing BDE-209 decreased as the pH and the initial dissolved oxygen content of the reaction solution increased, but increased as the proportion of water in the reaction solution increased. 相似文献
57.
Evi Kurniati Novi Arfarit Tsuyoshi Imai Takaya Higuchi Ariyo Kanno Koichi Yamamoto Masahiko Sekine 《环境科学学报(英文版)》2014,26(6):1223-1231
The use of filamentous fungi in bioremediation of heavy metal contamination has been developed recently. This research aims to observe the capability of filamentous fungi isolated from forest soil for bioremediation of mercury contamination in a substrate. Six fungal strains were selected based on their capability to grow in 25 mg/L Hg2+-contaminated potato dextrose agar plates. Fungal strain KRP1 showed the highest ratio of growth diameter, 0.831, thus was chosen for further observation.Identification based on colony and cell morphology carried out by 18S rRNA analysis gave a 98%match to Aspergillus flavus strain KRP1. The fungal characteristics in mercury(Ⅱ) contamination such as range of optimum pH, optimum temperature and tolerance level were 5.5–7 and 25–35℃ and 100 mg/L respectively. The concentration of mercury in the media affected fungal growth during lag phases. The capability of the fungal strain to remove the mercury(Ⅱ) contaminant was evaluated in 100 mL sterile 10 mg/L Hg2+-contaminated potato dextrose broth media in 250 mL Erlenmeyer flasks inoculated with 108spore/mL fungal spore suspension and incubation at 30℃ for 7 days. The mercury(Ⅱ) utilization was observed for flasks shaken in a 130 r/min orbital shaker(shaken) and nonshaken flasks(static) treatments. Flasks containing contaminated media with no fungal spores were also provided as control. All treatments were done in triplicate. The strain was able to remove 97.50%and 98.73% mercury from shaken and static systems respectively. A. flavus strain KRP1 seems to have potential use in bioremediation of aqueous substrates containing mercury(Ⅱ) through a biosorption mechanism. 相似文献
58.
59.
中亚热带针阔混交林土壤-大气界面释汞通量研究 总被引:4,自引:2,他引:2
为了揭示不同气候条件下森林与大气间汞交换的规律,应用动力学通量箱与Lumex RA 915+测汞仪联用技术,选择重庆缙云山国家级自然保护区为研究地点,于2011年4月~2012年3月对针阔混交林土/气界面释汞通量进行了为期1 a的连续监测,并考察了各环境因子对土壤释汞通量的影响.结果表明,缙云山针阔混交林林地土壤年平均释汞通量值为(16.82±6.70)ng·(m2·h)-1,明显高于欧美国家自然背景区;受光照、温度、相对湿度等气象因素以及亚热带地区森林植被生长变化规律影响,缙云山地区林地土壤释汞通量存在显著的季节性差异,暖季林地土壤释汞通量[(22.23±13.19)ng·(m2·h)-1]明显高于冷季[(6.01±4.05)ng·(m2·h)-1];通径分析结果表明林地土壤释汞通量的日变化特征和1 d中光照强度变化有密切关系,土温、气温和相对湿度与土壤释汞通量之间的显著相关关系可能是光照强度与土壤释汞通量相关关系的表象. 相似文献
60.
三峡库区消落带土壤汞形态分布与风险评价 总被引:18,自引:13,他引:5
为了解三峡库区消落带土壤中汞污染现状和环境风险,选择重庆14个区县的消落带,采集了192个土壤样品,分析其土壤总汞和汞形态分布,探讨其生物可利用性,对比研究和评估土壤总汞与汞赋存形态的污染水平和生态风险.结果表明,三峡库区消落带土壤中汞含量差异较大,土壤汞含量为22.4~393.5μg·kg-1,平均值为(84.2±54.3)μg·kg-1,76.6%的采样点土壤汞含量超过了三峡库区土壤汞背景值.土壤中的汞以残留态为主,不同汞形态所占比例为:水溶态汞4.1%、酸溶态15.5%、碱溶态汞18.3%、过氧化氢溶态汞10.9%、残留态汞51.3%.各区县土壤中生物可利用性汞(水溶态汞、酸溶态汞与碱溶态汞之和)平均含量为19.7~36.6μg·kg-1,生物可利用态汞占总汞的比例达到22.1%~51.6%.地累积指数和潜在生态危害指数评价结果均表明,三峡库区消落带土壤中汞赋存形态的污染水平和生态风险都较低,由生物可利用态汞带来的生态风险也很小;而对土壤总汞含量评价的结果明显偏大.因此,采用汞赋存形态进行污染现状和生态危害评价更能反映消落带土壤汞的环境风险. 相似文献