Assessing the Relative Contribution of Wastewater Treatment Plants to Levels of Metals in Receiving Waters for Catchment Management

The selection of control measures for reducing metal contamination in rivers has targeted point sources such as wastewater treatment plants (WWTPs) and industrial discharges without a proper evaluation of their relative contribution to metal loads at the catchment level. The necessity of controlling pollutant inputs in a sound and cost-effective way to prevent the deterioration of chemical and ecological quality of receiving waters has highlighted the need for appropriate source assessment. As metals in rivers emanate from a wide range of sources, it is necessary to understand their relative contribution in order to reduce effectively the concentrations in receiving waters. This study presents a simple method for calculating the relative contribution of WWTPs to levels of metals in receiving waters as applied to the Aire?CCalder catchment in the UK. In this catchment, the apportionments to WWTP effluents of metal levels in rivers were 37, 31, 36 and 60?% of total cadmium (Cd), lead (Pb), mercury (Hg) and nickel (Ni), respectively. Spatial metal distribution in rivers with maximum concentrations of 0.47???g?L^?1 for Cd, 8.54???g?L^?1 for Pb, 0.05???g?L^?1 for Hg and 10.17???g?L^?1 for Ni caused by the discharge of WWTP effluents was estimated. The findings demonstrate that the proposed approach using quantification of metal loads and estimation of concentrations in receiving waters could adequately calculate the relative contribution of WWTP effluents to metal levels in receiving waters. Applications to various river catchments using site-specific data would further validate the effectiveness of the approach proposed.     

Insecticide resistance status of Myzus persicae (Hemiptera: Aphididae) populations from peach and tobacco in mainland Greece

The susceptibility of 88 and 38 field samples of Myzus persicae (Sulzer) to imidacloprid and deltamethrin respectively was examined using the FAO dip test bioassay. The field samples were collected from tobacco and peach from various regions of Greece in the period from 2004 to 2006. In addition, 497, 349 and 370 clones originating from peach and tobacco were screened for the three known resistance mechanisms, elevated esterases, modified acetylcholinesterase (MACE) and knockdown resistance (kdr) respectively, using biochemical and DNA diagnostics. Most of the samples assayed with imidacloprid showed low resistance factors (RFs)-39% below 5 and 21% between 5 and 10. However, 9% of the samples (all from tobacco) showed relatively high RF values (24-73). Differences were found between crops, with higher RF values recorded in samples from tobacco than in those from peach. Bioassays with deltamethrin revealed the development of strong resistance in the populations examined. The RFs were mostly higher than 23, and in 29% of the samples they were extremely high (152-436). Finally, the three known resistance mechanisms were found in high frequencies in the populations examined, although some differences between crops and years were detected. The implications of the study for management schemes against M. persicae are discussed.     

Use of reference compounds in antioxidant activity assessment

The choice of reference compounds is examined as a "critical control point" of antioxidant activity assessment. Gallic, caffeic, sinapic, uric, and ascorbic acids, isoeugenol, and Trolox were tested using different redox (FRAP, Folin-Ciocalteu) and radical scavenging (DPPH*, ABTS*+, CBA, ORAC) assays. The ability to chelate transition metals was assessed to support some of the findings. Analytes were also tested in liposomes. On the basis of the findings, we do not recommend uric acid (due to solubility constrains) and ascorbic acid (due to fast degradation kinetics) as references. The behavior of the rest of the compounds could not always be attributed to typical structural characteristics. Selection of suitable reference compounds for in vitro antioxidant activity assays is not an easy task to achieve. The choice of reference compounds has to remain at the convenience of the researchers, with regard to the aim of the study.     

Defining critical habitat conditions for the conservation of three endemic and endangered cyprinids in a Mediterranean intermittent river before the onset of drought

相似文献   

Functional Teas from the Leaves of <Emphasis Type="Italic">Arbutus unedo</Emphasis>: Phenolic Content,Antioxidant Activity,and Detection of Efficient Radical Scavengers

The phenolic content/composition and antioxidant activity of hot/cold infusion and decoction from the leaves of Arbutus unedo were studied for the first time. 1,1-diphenyl-2-picrylhydrazyl (DPPH^●), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) radical cation (ABTS^●+), crocin-bleaching, copper-reducing, and liposome accelerated oxidation assays were used for the evaluation of the activity in vitro. In vivo, the extracts were examined for their ability to protect S. cerevisiae cells from H₂O₂ induced oxidative stress. An on-line high-performance liquid chromatography-DPPH^● assay was applied to identify potent radical scavengers and comment on their contribution to the total activity. The addition of leaves to boiling water (decoction) was the most appropriate practice to apply since the highest phenol intake (220.2 mg gallic acid/cup served) was obtained. Additionally, its antioxidant activity was equal or superior to that of the other extracts. Flavonols (~51–61 mg/g dry extract) were the main phenols in all the extracts, with quercitrin accounting for ~20% of the total phenol amount. The on-line DPPH^● method verified the high potency of the decoction and indicated as the most active radical scavengers, two galloylquinic acid derivatives and myricitrin, accounting for ~28–45% and ~11–13% of the total scavenging, respectively. Present data may contribute to the future exploitation of A. unedo leaves by the food industry for health-promoting herbal tea preparations and dietary supplements.