干旱区盐渍地景观危险度评价方法——以新疆渭干河-库车河流域为例

土壤的盐渍化是干旱区农业发展的主要障碍,也是影响绿洲生态环境稳定的重要因素。利用破碎度(C)、分离度(F)、优势度(D)等景观格局指数及景观脆弱度(S)建立了盐渍化景观危险度(SR)评价指数以研究渭干河-库车河流域盐渍化地的危险程度。选择新疆渭干河-库车河流域1989年和2001年Landsat-TM图像为本底数据,结合野外调查样本进行实例验证。研究表明,在12年期间,由于研究区内人类活动不断加强,景观结构变化导致盐渍化景观危险度指数明显增高,综合盐渍化危险度指数(SCR)由0.4832上升到0.5234,盐渍化危险度有扩大的趋势,评价结果与实际情况有较好的一致性。该方法对提高不同干旱区域土壤盐渍地危险度评价的准确性及定量化具有一定的参考意义。     

敌敌畏在颗粒物上吸附的支配因素

研究了敌敌畏在颗粒物(呼和浩特土壤和黄河水体沉积物)上的吸附行为,探讨了颗粒物性质如有机质含量、粘粒含量、阳离子交换量(CEC)、pH值和离子强度等因素对吸附的影响。结果表明:敌敌畏在2种颗粒物上的吸附过程均符合一级动力学规律,可用Freundlich等温式描述,吸附常数Kd为5. 822 0和11. 738 8;颗粒物性质与吸附常数的相关分析发现:支配敌敌畏在颗粒物上吸附的主要因素是有机质含量、pH值和离子强度,随着pH值的增加和离子强度的降低,敌敌畏在2种颗粒物上的吸附量增大。     

Polychlorinated biphenyls and chlorinated pesticides in mussels from the Egyptian Red Sea coast

The residues of 17 organochlorine pollutants were analyzed in bivalve Brachiodontes sp. collected from 11 different locations in April 2000 along the Egyptian Red Sea coast. The pollutants studied were 10 individual polychlorinated biphenyl (PCB) congeners, alpha,alpha,alpha-hexachlorocyclohexane (HCHs), cyclodienes (heptachlor, heptachlorepoxide, aldrin, dieldrin) and dichlorodiphenyltrichloroethanes (DDTs) (p,p'-DDE, p,p'-DDD and p,p'-DDT). The concentration of total DDTs ranged between 125 and 772 ng/g of wet weight whereas the concentration of the PCBs, HCHs and cyclodienes ranged from 6.7 to 66.4 ng/g; 16.2 to 183.4 ng/g and 8.8 to 221.6 ng/g of wet weight, respectively. The levels are low to moderate in relation to the published data from other coastal areas. The present results indicate low to moderate PCBs and pesticides contamination in the investigated mussels except DDTs.     

Residue levels of chlorinated hydrocarbon compounds in water and sediment samples from Nile branches in the Delta, Egypt.

Water and sediment samples were collected from eight different locations along the River Nile and its branches. Residues of hexachlorocyclohexane (HCH's), hexachlorobenzene (HCB), DDT's, cyclodienes and polychlorinated biphenyls (PCB's) were analyzed by GLC. Data on Grand Total (GT) concentration values pointed out that Rosetta Branch was more polluted with all components than Demietta Branch. Kafr El-Ziate was the most polluted location showing 1355.8 ng/L for water and 7396.9 ng/g for sediments, while Delta Barrage was the least polluted site. The concentrations of gamma-HCH were higher than the other isomers (alpha- and beta-HCH) in all studied sites. The results showed that HCB was the smallest pollutant at all locations on comparison with other chlorinated hydrocarbons. El-Mansoura, Rosetta and Kafr El-Ziate sites contained the highest concentrations of DDT's in both water and sediment samples. P,P'-DDE was dominate in all locations of water samples, but P,P'-DDT was in sediment samples. Also, the results showed the prominent presence of cyclodienes when compared with the other OC's compounds in sediment samples, especially Aldrin. Kafr El-Ziate was the most polluted location by PCB's, particularly the Ar1242. However, there were increasing levels of chlorinated hydrocarbons in the sediment samples parallel to percentage extractable organic matter (% EOM). Sediment/water ratios were calculated for all locations.     

Contamination of polycyclic aromatic hydrocarbons (PAHs) in microlayer and subsurface waters along Alexandria coast,Egypt

The residues of seven polycyclic aromatic hydrocarbons (PAHs) pollutants in microlayer and subsurface seawater samples collected from Alexandria coast, Egypt, were analyzed by gas chromatography–electron-impact mass spectrometry-selected ion monitoring mode (GC–MS-SIM). The pollutants studied were, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, chrysene and benzo[a]pyrene. Total PAH levels in microlayer ranged from 103 to 523 ng/l, while it ranged in subsurface samples from 13 to 120 ng/l. The Western Harbor location recorded the highest level of PAHs pollutant over all the other location for both subsurface and microlayer waters. The two major PAHs in microlayer water at the Western Harbor were fluorene and phenanthrene, making up 27% and 20% of the total PAHs, while the two major PAHs in subsurface water at the Eastern Harbor were phenanthrene and fluoranthene recording up 21% each of the total PAHs. The total PAH levels were generally in the nano-gram per liter for microlayer and subsurface seawater samples. The dominant PAHs in both subsurface and microlayer samples were fluoranthene, pyrene and benzo[a]pyrene. The microlayer enrichment factor at Alexandria’s Mediterranean coast was ranged from 29 for fluorene to 3 for phenanthrene and benzo[a]pyrene which showed PAHs concentration in the microlayer with an average of five times more than the total PAH in the subsurface samples.     

Photocatalytic removal of fenitrothion in pure and natural waters by photo-Fenton reaction

The photocatalytic removal kinetics of fenitrothion at a concentration of 0.5mgl(-1) in pure and natural waters were investigated in Fe(III)/H2O2/UV-Vis, Fe(III)/UV-Vis and H2O2/UV-Vis oxidation systems, with respect to decreases in fenitrothion concentrations with irradiation time using a solar simulator. Fenitrothion concentrations were determined by HPLC analysis. Furthermore, total mineralization of fenitrothion in these systems was evaluated by monitoring the decreases in DOC concentrations with solar simulator irradiation time by TOC analysis. It was shown that the degradation rate of fenitrothion was much faster in the Fe(III)/H2O2/UV-Vis system than the Fe(III)/UV-Vis and H2O2/UV-Vis systems in both pure and river waters. Consequently, the mineralization rate of fenitrothion was much faster in the Fe(III)/H2O2/UV-Vis system than in the other two systems. The high *OH generation rate measured in the Fe(III)/H2O2/UV-Vis system was the key to faster degradation of fenitrothion. Increases in the concentrations of H2O2 and Fe led to better final degradation of fenitrothion. These results suggest that the photo-Fenton reaction (Fe(III)/H2O2/UV-Vis) system is likely to be an effective method for removing fenitrothion from contaminated natural waters.     

石油污染土壤物化修复前后生物毒性效应

采用作物种子的发芽率作为生态指标对石油污染土壤进行毒性分析,并以蚯蚓为实验生物,研究了石油污染物的生物效应及其对土壤生态系统的影响.结果表明,不同的作物种子对石油污染表现出不同的耐受性,对照清洁土壤,大多数作物种子的萌发都明显受到石油污染的抑制,其中受石油污染影响最严重的是黄豆、蚕豆、玉米.相比之下,在不同石油污染水平下绿豆具有较高的耐受性,且种子发芽率均在90%以上.蚯蚓在受到污染胁迫时,在生理水平上会发生明显的变化,进而影响其存活和生长能力,实验观测到随着石油污染加重蚯蚓存活时间显著下降.在高污染水平石油污染的土壤中(石油污染水平>30 000 mg.kg-1),蚯蚓的耐性降低,仅可以存活5 d左右,说明石油烃对蚯蚓的毒性较大,主要是因为蚯蚓直接与石油接触导致其中毒脱水而死亡.处理后油田污染土,即使在污染水平很低(≈30 mg.kg-1)的情况下,蚯蚓存活时间依然很短(3 d左右),是因为经过石油醚处理过的土壤,其营养物质也随着石油而被处理掉,而土壤中有机质等营养物对蚯蚓的生存具有很大影响.     

Characterisation and identification of carbofuran-utilising bacteria isolated from agricultural soil

A total of 96 bacterial cultures were isolated from soil. Seventeen bacterial isolates were selected following their cultivation on solid media containing 100 mg · L^?1 carbofuran as the sole source of carbon and nitrogen. Of the 17 isolates, 10F, 11M, 17N, 23B and 26M were specifically chosen because of their relatively higher growth efficiency and genetic diversity based on Box-polymerase chain reaction analysis. These bacterial cultures had 16S rRNA gene sequences that were most similar to Acinetobacter baumannii (10F), Agrobacterium tumefaciens (11M), Ochrobactrum anthropi (17N), Escherichia coli (23B) and Agrobacterium tumefaciens (26M) with 97, 95, 93, 95 and 94% similarity in their 16S rDNA gene sequence, respectively. Degradation rates of carbofuran in soil inoculated with these isolates were 1.9, 1.5, 1.6, 1.7 and 1.6 times, respectively, faster in comparison with uninoculated soil after 10 days of incubation. The maximum degradation rates of carbofuran (45 and 91%) were detected in soil inoculated with A. baumannii (10F) after 10 and 20 days’ incubation, respectively. These data indicate that these isolates may have the potential for use in bioremediation of pesticide contaminated soil.     

Organochlorines and PCBs in Tilapia zillii from Lake El-Manzala,Egypt

Abstract

The mercury content has been determined in samples of fumarolic gases, phreatic waters, soil and vegetation collected at Vulcano, Aeolian Islands, Italy. Volcanic activity is demonstrated as a source of natural mercury pollution whose extent has been evaluated here by studying the contribution of different components of the surface environment. The possible influences for living organisms are examined.     

Microbial detoxification of metalaxyl in aquatic system

Four microorganisms, Pseudomonas sp. （ER2）, Aspergillus niger （ER6）, Cladosporium herbarum （ER4） and Penicilluim sp. （ER3）, were isolated from cucumber leaves previously treated with metalaxyl using enrichment technique. These isolates were evaluated for detoxification of metalaxyl at the recommended dose level in aquatic system. The effect of pH and temperature on the growth ability of the tested isolates was also investigated by measuring the intracellular protein and mycelia dry weight for bacterial and fungal isolates, respectively. Moreover, the toxicity of metalaxyl after 28 d of treatment with the tested isolates was evaluated to confirm the complete removal of any toxic materials （metalaxyl and its metabolites）. The results showed that the optimum degree pH for the growth of metalaxyl degrading isolates （bacterial and fungal isolates） was 7. The temperature 30℃ appeared to be the optimum degree for the growth of either fungal or bacterial isolates. The results showed that Pseudomonas sp. （ER2） was the most effective isolate in metalaxyl degradation followed by Aspergillus niger （ER6）, Cladosporium herbarum （ER4） and Penicilluim sp. （ER3）, respectively. There is no toxicity of metalaxyl detected in the supematant after 28 d of treatment with Pseudomonas sp. （ER2）. The results suggest that bioremediation by Pseudomonas sp. （ER2） isolate was considered to be effective method for detoxification of metalaxyl in aqueous media.