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PubMedDate not supplied

Data quality of PAH determinations in environmental monitoring.

The sources of uncertainty affecting measurements of pollutants include sample collection, handling and stocking, and analytical procedure. With regard to chemical analysis, MS detection offers a series of advantages for resolving complex mixtures and identify and quantify analytes present at very small extents. Nevertheless, it presents some problems of reproducibility, which can affect the quality of quantitative data. PAH represent key-compounds among atmospheric pollutants and are usually evaluated by means of dedicated methods comprising MS detection. Based upon the above considerations, an analytical method has been standardized, suitable for determining PAH in atmospheric aerosols and diesel particulate exhausts. To test the procedure, both diesel particulate and urban aerosol NIST reference materials (SRM-2975 and SRM-1649A, respectively) have been processed and the results have been compared with certified and/or literature data. The results obtained are shortly discussed.

Aerosols↗
PubMed2006

Toxicity testing of leachate from waste landfills using medaka (Oryzias latipes) for monitoring environmental safety.

To investigate the environmental safety of waste disposal landfill sites and of land reclaimed from such sites, we evaluated the toxicity of leachate from these sites by a combination of bioassays in the Japanese killifish medaka Oryzias latipes. We tested for lethal toxicity in adult and larval medaka and for hatching inhibition of embryos from eggs. As biochemical evidence of the effects of leachate exposure, CYP1A (EROD activity) and vitellogenin (Vtg) were induced. We also bioassayed water-treated leachate and downstream river water. Leachate solution was lethal to larval and adult medaka. Embryo hatchability was inhibited, and abnormal hatching, spinal deformity and anisophthalmia occurred in embryos exposed to leachate solution. CYP1A was induced by exposure to leachate solution diluted to 1.0%, and EROD activity was significantly higher than in control. Vtg and unknown proteins were induced in the sera of male medaka exposed to the diluted leachate solution. Conventional water treatments worked effectively to remove toxic compounds but did not work well to remove element ions, including heavy metals. Treated leachate produced neither lethal toxicity nor hatching abnormalities during the exposure period. Fish toxicity tests for leachate would be useful for monitoring the environmental safety of landfill sites.

Animals↗
PubMed2005

Amphipod acute and chronic sediment toxicity assessment in estuarine environmental monitoring: An example from Ria de Aveiro, NW Portugal.

This paper presents a comprehensive estuarine sediment toxicity survey, using acute and full life-cycle tests with an indigenous species, the amphipod Corophium multisetosum. In the acute test, adult specimens were exposed to sediments from 144 sites for 10 days. In the full life-cycle test, 5-7 days old specimens, obtained in laboratory cultures, were exposed during 21 days to sediments from 56 sites. Three endpoints were considered: survival, for the acute and the chronic test and fecundity (number of gravid females per replicate at the end of the exposure) and growth (weight increase), for the chronic test. In the acute tests, adult survival was high overall and almost no stressed areas could be recognized in the estuary. This image was not reflected by the chronic endpoints, in particular growth and fecundity, which, corrected for the number of survivors, was the most affected descriptor. The chronic data could not be related to the baseline sediment variables analysed (grain-size, total organic content and redox potential), suggesting that these play no part in the biological responses. Results indicate that a tiered sediment bioassessment approach including an initial comprehensive ecotoxicological screening phase should not rely solely upon acute responses, although these are obtained from simpler and more rapid laboratory testing procedures.

Amphipoda↗
PubMed2006

Environmental monitoring of land-use and land-cover changes in a Mediterranean region of Turkey.

Unprecedented rates of human-induced changes in land use and land cover (LULC) at local and regional scales lead to alterations of global biogeochemical cycles. Driving forces behind LULC changes mainly include rapid growth rates of population and consumption, lack of valuation of ecological services, poverty, ignorance of biophysical limitations, and use of ecologically incompatible technologies. One of the major ecological tragedies of the commons in a Mediterranean region of Turkey is the loss of Lake Amik at the expense of increasing the area of croplands, which used to provide vital ecosystem goods and services for the region. In this study, we aimed at quantifying the effects of past land-use transitions on soil organic carbon (SOC) pools (0-20 cm) in a Mediterranean region of 3930 km(2), between 1972 and 2000. LULC changes were quantified from a time series of satellite images of Landsat-MSS in 1972, Landsat-5 TM in 1987, and Landsat-7 ETM+ in 2000 using geographic information systems. The study showed that the increase in croplands between 1972 and 1987 took place at the expense of the irreversible losses of Lake Amik and its related wetlands of over 53 km(2). In the period of 1972 to 2000, croplands, settlements, and evergreen forests increased by 174%, 106%, and 14%, respectively. The increase in settlements occurred mostly to the detriment of croplands. Given the average rates of all the land-use transitions, and associated changes in SOC density for the study region of 3930 km(2), total SOC pool was estimated to decrease by 14.1% from 130.1 Mt in 1972 to 111.7 Mt in 2000.

Agriculture↗
PubMed1999

Higher plant assays for the detection of chromosomal aberrations and gene mutations-a brief historical background on their use for screening and monitoring environmental chemicals.

Higher plants are recognized as excellent indicators of cytogenetic and mutagenic effects of environmental chemicals and are applicable for the detection of environmental mutagens both indoor and outdoor. They are highly reliable bioassays with a high sensitivity for monitoring and testing for genotoxins. A brief review of major steps in the development of higher plant genotoxic assays is given.

Air Pollution, Indoor↗
PubMed2004

Stress responsive bacteria: biosensors as environmental monitors.

The delicate and dynamic balance of the physiological steady state and its maintenance is well characterized by studies of bacterial stress response. Through the use of genetic analysis, numerous stress regulons, their physiological regulators and their biochemical processes have been delineated. In particular, transcriptionally activated stress regulons are subjects of study and application. These regulons include those that respond to macromolecular damage and toxicity as well as to nutrient starvation. The convenience of reporter gene fusions has allowed the creation of biosensor strains, resulting from the fusion of stress-responsive promoters with a variety of reporter genes. Such cellular biosensors are being used for monitoring dynamic systems and can report the presence of environmental stressors in real time. They provide a greater range of sensitivity, e.g. to sub-lethal concentrations of toxicants, than the simple assessment of cell viability. The underlying physiological context of the reporter strains results in the detection of bioavailable concentrations of both toxicants and nutrients. Culture conditions and host strain genotypes can be customized so as to maximize the sensitivity of the strain for a particular application. Collections of specific strains that are grouped in panels are used to diagnose targets or mode of action for unknown toxicants. Further application in massive by parallel DNA and gene fusion arrays greatly extends the information available for diagnosis of modes of action and may lead to development of novel high-throughput screens. Future studies will include more panels, arrays, as well as single reporter cell detection for a better understanding of the population heterogeneity during stress response. New knowledge of physiology gained from further studies of novel systems, or using innovative methods of analysis, will undoubtedly yield still more useful and informative environmental biosensors.

Bacteria↗
PubMed1985

Environmental monitoring for genotoxicity: in vivo sister chromatid exchange in the house mouse (Mus musculus).

Sister chromatid exchange (SCE) values were determined in bone marrow cells isolated from mouse (Mus musculus) femurs after injections of 5-bromo-2'-deoxyuridine (BrdU) and 5-fluorodeoxyuridine (FrdU). Male mice of C3H/J, C57BL/6J, and DBA/2 strains maintained in the laboratory gave mean SCE values of 3.42 +/- 0.07, 3.62 +/- 0.08, and 3.97 +/- 0.13, respectively. Males obtained from natural populations of southwestern Ontario had a higher mean SCE value (6.02 +/- 0.16), as did inbred males maintained in outdoor enclosures for at least 3 weeks (5.07 +/- 0.22). Wild mice housed in the laboratory for 9 months or longer had SCE values similar to laboratory bred mice (3.46 +/- 0.05). The SCE values in wild-caught mice were inversely proportional (r = -0.49) to the distance between the sites where these animals were collected and the nearest major industrial center. Based on these results, SCE analysis in mice is proposed as a possible first-line monitoring procedure for the detection of general changes in environmental genotoxicity.

Animals↗
PubMed2005

16S rRNA gene-based oligonucleotide microarray for environmental monitoring of the betaproteobacterial order "Rhodocyclales".

For simultaneous identification of members of the betaproteobacterial order "Rhodocyclales" in environmental samples, a 16S rRNA gene-targeted oligonucleotide microarray (RHC-PhyloChip) consisting of 79 probes was developed. Probe design was based on phylogenetic analysis of available 16S rRNA sequences from all cultured and as yet uncultured members of the "Rhodocyclales." The multiple nested probe set was evaluated for microarray hybridization with 16S rRNA gene PCR amplicons from 29 reference organisms. Subsequently, the RHC-PhyloChip was successfully used for cultivation-independent "Rhodocyclales" diversity analysis in activated sludge from an industrial wastewater treatment plant. The implementation of a newly designed "Rhodocyclales"-selective PCR amplification system prior to microarray hybridization greatly enhanced the sensitivity of the RHC-PhyloChip and thus enabled the detection of "Rhodocyclales" populations with relative abundances of less than 1% of all bacteria (as determined by fluorescence in situ hybridization) in the activated sludge. The presence of as yet uncultured Zoogloea-, Ferribacterium/Dechloromonas-, and Sterolibacterium-related bacteria in the industrial activated sludge, as indicated by the RHC-PhyloChip analysis, was confirmed by retrieval of their 16S rRNA gene sequences and subsequent phylogenetic analysis, demonstrating the suitability of the RHC-PhyloChip as a novel monitoring tool for environmental microbiology.

Base Sequence↗