PubMed · 14685179
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Jonathan Knight. 2003-12-18. Scientists attack industrial influence.. https://doi.org/10.1038/426741b
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Microalgal species vary in their sensitivity to the triazine herbicide, atrazine. This study examined both atrazine uptake and cellular characteristics of microalgae to determine if either can be used to predict algal sensitivity. Standard toxicity tests were performed on five microalgal species, each representing a different algal division or habitat. Test species listed in order of increasing sensitivity were: Isochrysis galbana, Dunaliella tertiolecta, Phaeodactylum tricornutum, Pseudokirchneriella subcapitata, and Synechococcus sp. Each species was exposed to 14C-atrazine at its growth rate EC50 concentration (44-91 microg/L). At five time-points over 96 h, samples were filtered to collect algae and washed with unlabeled atrazine to displace labeled atrazine loosely absorbed to the cell surface. Radioactivity present on filters and in the growth medium was measured by liquid scintillation counting. Relationships between algal species-sensitivity to atrazine and compound uptake, cell dry weight, cell volume, and cell surface area were determined by linear regression analysis. Cell size measurements (based on dry weight, biovolume, and surface area) were significantly correlated with atrazine uptake (R2 > 0.45, P-value < 0.05). There was a significant correlation between atrazine uptake and species-sensitivity to atrazine (R2 = 0.5413 , P-value = 0.0012). These results indicate that smaller cells with greater surface area to volume ratios will incorporate more atrazine, and in general, will be more sensitive to atrazine exposure. However, I. galbana, with small cell size and relatively high atrazine uptake was the least sensitive species tested. This species and others may have mechanisms to compensate for atrazine stress that make predicting responses of microalgal communities difficult.
The UK Farm-Scale Evaluations (FSE) compared the effects on biodiversity of management of genetically modified herbicide-tolerant (GMHT) spring-sown crops with conventional crop management. The FSE reported larger weed abundance under GMHT management for fodder maize, one of three crops studied. Increased seed production may be important for the long-term persistence of these arable weeds and may benefit invertebrates, small mammals and seed-eating birds. In three-quarters of FSE maize fields, growers used atrazine on the conventionally managed half, reflecting contemporary commercial practice. Withdrawal of the triazine herbicides atrazine, simazine and cyanazine from approved lists of EU chemicals could therefore reduce or even reverse the reported benefits of GMHT maize. Here we analyse effects of applications of triazine herbicides in conventional maize regimes on key indicators, using FSE data. Weed abundances were decreased greatly relative to all other regimes whenever atrazine was applied before weeds emerged. Here, we forecast weed abundances in post-triazine herbicide regimes. We predict weed abundances under future conventional herbicide management to be considerably larger than that for atrazine used before weeds emerged, but still smaller than for the four FSE sites analysed that used only non-triazine herbicides. Our overall conclusion is that the comparative benefits for arable biodiversity of GMHT maize cropping would be reduced, but not eliminated, by the withdrawal of triazines from conventional maize cropping.
In most medical and environmental applications of biosensors, only single analytes are determined. However, the monitoring of several analytes is obviously preferable in order to gather more information about the sample under analysis. In line with this, different technologies are being developed to obtain multi-analyte sensors. In this paper, an analytical method for the simultaneous determination of three different contaminants-atrazine, isoproturon, and estrone-in natural waters by using an optical immunosensor prototype, the so-called "RIver ANAlyser" (RIANA), is described. RIANA is based on a rapid solid-phase fluoroimmunoassay that takes place at an optical transducer chip. The transducer surface is chemically modified with three analytes derivatives placed in different discrete locations. The sensor surface can be regenerated thus allowing the performance of several measurements with the same transducer. Each test cycle, including one regeneration step, is accomplished in 15 min. Detection limits achieved were 0.155, 0.046, and 0.084 microg/l, for atrazine, isoproturon, and estrone, respectively. Satisfactory repetition, with relative standard deviations between 1.06 and 6.98%, was obtained. Excluding a minor non-specifical binding of the isoproturon antibodies, no cross-reactivity effects were observed. Matrix effects were significant only in the case of wastewater samples. Biosensor measurements were validated using conventional liquid chromatography-mass spectrometry. The results obtained with both techniques were in good agreement.