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351.
352.
酸雨对建筑材料的影响及防治研究综述 总被引:1,自引:0,他引:1
综合分析了酸雨对建筑外墙的涂料、石材、混凝土等主要建筑构件的腐蚀原理,并提出了防治措施,来预防酸雨对建筑材料的侵害。 相似文献
353.
以坡耕地柑桔园为研究对象,地表覆盖方式采用对照、秸秆覆盖和地膜覆盖3个处理,实验采用完全方案。结果表明,在本实验条件下,坡地地膜覆盖处理一定程度增加了径流量,而秸秆覆盖处理与对照每次降雨径流量基本相当;各处理土壤氮磷养分均有一定程度的流失,以氮素流失量较高,磷素流失量相对较低;在地膜覆盖条件下,柑桔园地表径流中N、P流失量较高,其总氮和总磷流失系数分别达0054%和0064%,而秸秆覆盖总氮和总磷流失系数最低;对不同地表覆盖方式柑桔园地表径流水体氮素形态特征分析表明,可溶性氮素占总氮的比例较高,可溶性氮素中又以NO-3 N为主,而NH+4 N所占的比重较低。以上结果说明,在丹江口库区,氮素污染风险要高于磷,防控的主要矛盾是氮,而秸秆覆盖是减少坡耕地养分流失较好的管理措施 相似文献
354.
Xiuyi Hua Deming Dong Xiaoou Ding Fan Yang Xu Jiang Zhiyong Guo 《Environmental science and pollution research international》2013,20(1):413-420
The effects of solution pH on adsorption of trace metals to different types of natural aquatic solid materials have been studied extensively, but few studies have been carried out to investigate the effect of pH at which the solid materials were formed on the adsorption. The purpose of present study is to examine this effect of culture pH on metal adsorption to natural freshwater biofilms. The adsorption of Pb and Cd to biofilms which were developed at different culture pH values (ranging from 6.5 to 9.0) was measured at the same adsorption pH value (6.5). The culture pH had considerable effects on both composition and metal adsorption ability of the biofilms. Higher culture pH usually promoted the accumulation of organic material and Fe oxides in the biofilms. The culture pH also affected the quantity and species of algae in the biofilms. The adsorption of Pb and Cd to the biofilms generally increased with the increase of culture pH. This increase was minor at lower pH range and significant at higher pH range and was more remarkable for Cd adsorption than for Pb adsorption. The notable contribution of organic material to the adsorption at higher culture pH values was also observed. The profound impacts of culture pH on adsorption behavior of biofilms mainly resulted from the variation of total contents of the biofilm components and were also affected by the alteration of composition and properties of the components. 相似文献
355.
Managing the Three-Rivers Headwater Region, China: From Ecological Engineering to Social Engineering 总被引:1,自引:0,他引:1
Yiping Fang 《Ambio》2013,42(5):566-576
The three-rivers headwater region (THRHR) of Qinghai province, China plays a key role as source of fresh water and ecosystem services for central and eastern China. Global warming and human activities in the THRHR have threatened the ecosystem since the 1980s. Therefore, the Chinese government has included managing of the THRHR in the national strategy since 2003. The State Integrated Test and Demonstration Region of the THRHR highlights the connection with social engineering (focus on improving people’s livelihood and well-being) in managing nature reserves. Based on this program, this perspective attempts a holistic analysis of the strategic role of the THRHR, requirements for change, indices of change, and approaches to change. Long-term success of managing nature reserves requires effective combination of ecological conservation, economic development, and social progress. Thus, the philosophy of social engineering should be employed as a strategy to manage the THRHR. 相似文献
356.
Yanwei Zhang Hongwen Sun Fang Liu Yuanyuan Dai Xuebo Qin Yuefei Ruan Lijie Zhao Zhiwei Gan 《Chemosphere》2013
To interpret the distribution of hexabromocyclododecanes (HBCDs) in various organisms, we measured the concentrations and diastereomer and enantiomer profiles of HBCDs in 21 different species of limnic and marine cohorts from Tianjin, China. The concentration ranges of HBCDs in limnic and marine organisms were 64.3–1111 ng g−1 lw and 85.5–989 ng g−1 lw, respectively. Living habitat and feeding habits had important impacts on HBCD diastereomer distribution. Most of the species appeared to preferentially select (+)-α-, (−)-β- and (−)-γ-HBCD. There is a tendency that the total and α-HBCDs were magnified as trophic level increased with trophic magnification factors (TMFs) around 2. The concentrations of HBCDs in the limnic and marine fishes were highest in the liver, followed by the gill, skin, and muscle. In terrestrial plants, the highest concentrations of HBCDs were observed in the leaf, followed by the root and the rhizosphere soil. Plants showed enantioselectivity for HBCD enantiomers, which varied with plant species and organs (leaf vs. root) of the same plant. Higher estimated daily intakes (EDIs) of HBCDs were observed from fish than from wheat. 相似文献
357.
Benzo[a]pyrene (BaP) biodegradation by Stenotrophomonas maltophilia was studied under the influence of co-existed Cu(II) ions. About 45% degradation was achieved within 3 d when dealing with 1 mg L?1 BaP under initial natural pH at 30 °C; degradation reached 48% in 2 d at 35 °C. Efficacy of BaP biodegradation reached the highest point at pH 4. In the presence of 10 mg L?1 Cu(II) ions, the BaP removal ratio was 45% on 7th day, and maintained stable from 7 to 14 d at 30 °C under natural pH. The favorable temperature and pH for BaP removal was 25 °C and 6.0 respectively, when Cu(II) ions coexisted in the solutions. Experiments on cometabolism indicated that S. maltophilia performed best when sucrose was used as an additional carbon source. GC–MS analysis revealed that the five rings of BaP opened, producing compounds with one or two rings which were more bioavailable. 相似文献
358.
Dong Qing Zhang Tao Hua Richard M. Gersberg Junfei Zhu Wun Jern Ng Soon Keat Tan 《Chemosphere》2013,90(4):1568-1572
Uptake, accumulation and translocation of caffeine by Scirpus validus grown in hydroponic condition were investigated. The plants were cultivated in Hoagland’s nutrient solution spiked with caffeine at concentrations of 0.5–2.0 mg L?1. The effect of photodegradation on caffeine elimination was determined in dark controls and proved to be negligible. Removal of caffeine in mesocosms without plants showed however that biodegradation could account for about 15–19% of the caffeine lost from solutions after 3 and 7 d. Plant uptake played a significant role in caffeine elimination. Caffeine was detected in both roots and shoots of S. validus. Root concentrations of caffeine were 0.1–6.1 μg g?1, while the concentrations for shoots were 6.4–13.7 μg g?1. A significant (p < 0.05) positive correlation between the concentration in the root and the initial concentrations in the nutrient solution was observed. The bioaccumulation factors (BAFs) of caffeine for roots ranged from 0.2 to 3.1, while BAFs for shoots ranged from 3.2 to 16.9. Translocation from roots to shoots was the major pathway of shoot accumulation. The fraction of caffeine in the roots as a percentage of the total caffeine mass in solution was limited to 0.2–4.4% throughout the whole experiment, while shoot uptake percentage ranged from 12% to 25% for caffeine at the initial concentration of 2.0 mg L?1 to 50–62% for caffeine at the initial concentration of 0.5 mg L?1. However, a marked decrease in the concentration of caffeine in the shoots between d-14 and d-21 suggests that caffeine may have been catabolized in the plant tissues subsequent to plant uptake and translocation. 相似文献
359.
The kinetics and mechanism for degradation of omethoate (OMT) by catalytic ozonation with Fe(III)-loaded activated carbon (Fe@AC) were investigated in this study with focus on identification of degradation byproducts. The rate constants of OMT reacting with ozone and hydroxyl radical (OH) were determined to be 0.04 and 5.3 × 108 M?1 s?1 at pH 7.5 and 20 °C, respectively. OMT was predominantly degraded by OH in the catalytic ozonation with Fe@AC. The high-molecular-weight degradation byproducts identified were O,O,O-trimethyl phosphoric ester (TMP), pyrrolidin-2-one, N-methyl-2-sulfanylacetamide, 2-(methylthio)acetamide, O,O,S-trimethylthiophosphate (STMP), and N-methyl-2-(methylthio)acetamide. Besides, low-molecular-weight organic acids and inorganic anions were also detected and quantified, including formic, acetic and oxalic acids as well as nitrate, sulfate and phosphate ions. In the catalytic ozonation, TMP and phosphate were two major P-containing byproducts resulting from OMT degradation. The toxicity of OMT solution gradually decreased during the catalytic ozonation, indicating that Fe@AC is a safe catalyst for OMT removal by ozone in water. 相似文献
360.
Air–water exchange fluxes of polycyclic aromatic hydrocarbons (PAHs) were simultaneously measured in air and water samples from two sites on the Kenting coast, located at the southern tip of Taiwan, from January to December 2010. There was no significant difference in the total PAH (t-PAH) concentrations in both gas and dissolved phases between these two sites due to the less local input which also coincided to the low levels of t-PAH concentration; the gas and dissolved phases averaged 1.29 ± 0.59 ng m?3 and 2.17 ± 1.19 ng L?1 respectively. The direction and magnitude of the daily flux of PAHs were significantly influenced by wind speed and dissolved PAH concentrations. Individual PAH flux ranged from 627 ng m?2 d?1 volatilization of phenanthrene during the rainy season with storm–water discharges raising dissolved phase concentration, to 67 ng m?2 d?1 absorption of fluoranthene during high wind speed periods. Due to PAH annual fluxes through air–water exchange, Kenting seawater is a source of low molecular weight PAHs and a reservoir of high molecular weight PAHs. Estimated annual volatilization fluxes ranged from 7.3 μg m?2 yr?1 for pyrene to 50 μg m?2 yr?1 for phenanthrene and the absorption fluxes ranged from ?2.6 μg m?2 yr?1 for chrysene to ?3.5 μg m?2 yr?1 for fluoranthene. 相似文献