Aliphatic and aromatic halocarbons as potential mutagens in drinking water

Chlorinated phenols are either products of industrial chemical processes or the result of chlorination of drinking water. Often, the formation of chlorinated phenols is based upon naturally occurring phenol. The following chlorinated phenols have been selected for testing in the Ames‐test for their mutagenic activity: 3‐chlorophenol, 4‐chlorophenol, 2,3,6‐, 2,4,5‐, 2,4,6‐trichlorophenol, 4‐chloro‐2‐methylphenol and 4‐chloro‐3‐methylchlorophenol. The tester strains TA97, TA98, TA100 and TA104 were employed. All tested compounds produced mutagenic activity at least in one tester strain. The highest numbers of revertants were detected for 2,3,6‐ and 2,4,6‐trichlorophenol. But in contrast to the other substances, these two induced only frameshift mutations in presence of a metabolizing system. The evidence of their presence in drinking water and of their mutagenic activity makes them to a potential health hazard.     

Cadmium-induced DNA damage and mutations in Arabidopsis plantlet shoots identified by DNA fingerprinting

Random amplified polymorphic DNA (RAPD) test is a feasible method to evaluate the toxicity of environmental pollutants on vegetal organisms. Herein, Arabidopsis thaliana (Arabidopsis) plantlets following Cadmium (Cd) treatment for 26 d were screened for DNA genetic alterations by DNA fingerprinting. Four primers amplified 20-23 mutated RAPD fragments in 0.125-3.0 mg L⁻¹ Cd-treated Arabidopsis plantlets, respectively. Cloning and sequencing analysis of eight randomly selected mutated fragments revealed 99-100% homology with the genes of VARICOSE-Related, SLEEPY1 F-box, 40S ribosomal protein S3, phosphoglucomutase, and noncoding regions in Arabidopsis genome correspondingly. The results show the ability of RAPD analysis to detect significant genetic alterations in Cd-exposed seedlings. Although the exact functional importance of the other mutated bands is unknown, the presence of mutated loci in Cd-treated seedlings, prior to the onset of significant physiological effects, suggests that these altered loci are the early events in Cd-treated Arabidopsis seedlings and would greatly improve environmental risk assessment.     

Gas chromatography with atomic absorption detection for the determination of alkyl selenide compounds in the breath of mice after administration of different selenium compounds

Quantitative determination of dimethylselenide and dimethyldiselenide in the breath of mice after addition of different selenium compounds to the drinking water is described. Breath samples are collected with a cryogenic trap and analyzed by gas chromatography with atomic absorption spectrometric detection. Detection limits down to 0.2 ng/100 g body weight are obtained.

The pulmonary excretion of selenium metabolites after oral administration via drinking water or after intraperitoneal injection appears to be negligible. The bioconversion of the different selenium species is discussed.     

绿色施工评价指标体系与方法研究

作为传统的高能耗产业,建筑业的节能减排对我国节能减排工作大局意义重大。绿色施工以节能减排为核心理念,是建筑业实施可持续发展战略重要措施。通过对我国建筑施工活动中的污染源和能耗源进行追溯和辨识,综合管理、技术、经济等要素,并参照我国绿色施工相关规定,探讨构建了基于我国国情的绿色施工综合评价标准体系,进而利用突变级数法,设计了绿色施工综合评价方法。结合相关工程进行实例评价,结果表明该评价指标体系与方法评价结论客观与准确,并可以发现建筑企业绿色施工生产活动中缺陷,提高企业管理水平,促进技术创新,降低生产成本。     

Mutagenicity of atmospheric air and snow cover in the city of Syktyvkar estimated by the somatic mutation test inTradescantia (Clone 02) stamen hairs

Genotoxicity of atmospheric air was studied in Syktyvkar for three years (1995–1997) using the test of somatic mutations inTradescantia (clone 02) stamen hairs. The data obtained indicate local air pollution in the city. The tested samples of snowmelt, where Ni⁺ and Zn²⁺ ions were the main pollutants, had a high teratogenic effect on stamen hairs. The somatic mutation rate similar to that in the control group was obtained in the experiment with only one sample, in which the total content of metal ions was the lowest.     

Identification of two mutations for ataxia telangiectasia among the Druze community

Ataxia telangiectasia (AT) is a rare autosomal recessive disease characterized by progressive cerebellar ataxia, immunodeficiency, susceptibility to lymphoreticular malignancies and cancer predisposition, hypersensitivity to ionic radiation and chromosomal instability. In this study, we report a founder effect of AT with two different mutations: 1339 C > T and 6672 del GG together with 6677 del TACG, found in four Israeli Druze clans originating from three different Druze centers in the Middle East (Lebanon, Syria and Jordan). The 1339 C > T mutation, which results in a stop codon at position 447 of the ATM protein, was observed in two unrelated clans originating from Lebanon and Jordan. The 6672 del GG/6677 del TACG mutation was observed in two unrelated clans originating from Syria and Lebanon. In the present study, simple and fast detection assays were developed for both mutations. The ability to identify AT carriers routinely provides a unique opportunity for prenatal diagnosis, genetic counseling as well as marriage guidance in the Druze community. Copyright © 2004 John Wiley & Sons, Ltd.     

Genomic instability in the bank vole: Population-ecological aspects

Chromosome aberration frequency in relation to population dynamics and demographic parameters was studied for six years in a bank vole population in the Middle Urals. The frequencies of structural chromosome aberrations, chromatid gaps, aneuploidy, and polyploidy in males and females and in animals of different ages did not differ significantly. In the breeding period, the frequencies of structural aberrations and changes in chromosome number increased in the somatic cells of voles. Highly significant differences between the levels of chromosome instability in different years manifested a tendency toward a negative correlation with population size.