Air quality biomonitoring in agricultural areas nearby to urban and industrial emission sources in Córdoba province,Argentina, employing the bioindicator Tillandsia capillaris

The air quality in agricultural areas close to industrial emission sources (chemical, metallurgical and cement plant) was evaluated through a biomonitoring study employing the epiphytic species Tillandsia capillaris Ruíz and Pav. f. capillaris. Plants were collected from a non-contaminated area in the province of Córdoba (reference site) and transplanted back to this site and into three industrial areas representing different emission sources of air pollutants: cement plant, chemical and metallurgical industries. Biomonitors were exposed to ambient air for four periods of 3 months each during one year (for determination of physiological parameters) and for four periods of 6 months each during two years (for determination of trace elements). In the exposure period coinciding with the winter season (i.e., the dry season) the plants showed the strongest global physiological damage, possibly due to higher air pollutant concentrations. The comparison among study areas indicates the highest values of foliar damage index at the chemical industries sites, possibly due to the emission of oxidizing pollutants. On the other hand, heavy metals and trace element concentrations (V, Fe, Co, Cu, Br, Ni, Zn and Pb) were associated mainly with metallurgical industries, although the chemical industries and the cement plant were associated with Ni, Zn and Ca accumulation in the biomonitor, respectively. Considering that these sites with high industrial activity are located close to soybean producing areas, further environmental and toxicological studies are necessary, taking into account food safety and human health.     

Ausländische Gartenschriften

Ohne Zusammenfassung     

Simplified spectrophotometric assay for microsomal 3-hydroxy-3-methylglutaryl CoA reductase by measurement of coenzyme A

A new assay for 3-hydroxy-3-methylglutaryl CoA reductase (mevalonate:NADP oxidoreductase [acylating CoA], EC 1.1.1.34) is based upon the measurement of released coenzyme A (SH) during the reduction of 3-hydroxy-3-methylglutaryl CoA to mevalonate. Coenzyme A was measured in the presence of dithiothreitol, required for activity, by reaction with 5,5'-dithiobis(2-nitrobenzoic acid). Sodium arsenite forms a complex with the dithiol, but not with monothiols. Thus, reduced coenzyme A reacts instantaneously with the reagent and dithiothreitol reacts slowly. The absorbance due to the coenzyme A-5,5'-dithiobis(2-nitrobenzoic acid) reaction is determined by extrapolating the linear (dithiol) absorbance-time curve to the time of addition of the reagent. After subtraction of control absorbance (deletion of NADPH), the concentration of CoA-SH is calculated from epsilon(max) = 1.36 x 10(4) at 412 nm. The method of protein removal and reduction of sulfhydryl groups on the enzyme are critical. This method provides an immediate assay. Recovery of reduced coenzyme A was 98.7%. The assay is applicable for microsomes or purified enzyme and has an effective range of 0.5-50 nmoles of coenzyme A. It was applied to kinetic measurement of the pigeon liver microsomal enzyme reaction. The apparent K(m) value for 3-hydroxy-3-methylglutaryl CoA was 1.75 x 10(-5) M, and for NADPH the value was 6.81 x 10(-4) M. This method was compared with the dual-label method at high and low levels of activity. The data were not statistically different.