Zbyněk Večeřa

Ozone flux over a Norway spruce forest and correlation with net ecosystem production.

Daily ozone deposition flux to a Norway spruce forest in Czech Republic was measured using the gradient method in July and August 2008. Results were in good agreement with a deposition flux model. The mean daily stomatal uptake of ozone was around 47% of total deposition. Average deposition velocity was 0.39 cm s(-1) and 0.36 cm s(-1) by the gradient method and the deposition model, respectively. Measured and modelled non-stomatal uptake was around 0.2 cm s(-1). In addition, net ecosystem production (NEP) was measured by using Eddy Covariance and correlations with O3 concentrations at 15 m a.g.l., total deposition and stomatal uptake were tested. Total deposition and stomatal uptake of ozone significantly decreased NEP, especially by high intensities of solar radiation.

Preconcentration and determination of 2,4,5-trichlorophenol in air using a wet effluent denuder and high-performance liquid chromatography

Abstract A wet effluent diffusion denuder was used for the preconcentration of gaseous 2,4,5-trichlorophenol (2,4,5-TCP) from air. The wet denuder function is based on capturing gaseous pollutants from air in a film of absorbing liquid that flows continuously down the inner wall of the wet denuder. The air passes through the cylindrical wet denuder under laminar flow conditions. Water (adjusted to pH 8.5) was employed as absorbing liquid. The concentration of 2,4,5-TCP was determined using a liquid picochromatography with a reversed-phase C 18 stationary phase and UV detection at 218 nm. The detection limit was 685 ng m −3 The measuring systems enables results to be obtained at 7-min intervals.

Wet effluent diffusion denuder technique and determination of volatile organic compounds in air: I. Oxo compounds (alcohols and ketones)

The wet effluent diffusion denuder (WEDD) preconcentration technique for the determination of methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 1-pentanol, acetone, methyl ethyl ketone, diethyl ketone and methyl n-propyl ketone in air is discussed. The compounds are continuously collected into a thin film of deionized water flowing down the inner wall of the cylindrical wet effluent diffusion denuder. The concentrate is analysed by gas chromatography. Detection limits of alcohols and ketones are as low as 1 microg/l (GC-flame ionization detection) and/or 1 ng/l (GC-MS). This technique could be applicable for the continuous monitoring of ppb (v/v) levels of both alcohols and ketones in the air.

Annular diffusion denuder for simultaneous removal of gaseous organic compounds and air oxidants during sampling of carbonaceous aerosols

A specially designed annular diffusion denuder for simultaneous removal of organic gaseous compounds and atmospheric oxidants in carbonaceous aerosol sampling is presented. Various kinds of denuder coatings were compared with respect to the collection efficiency of both organic gaseous compounds and NO(2) and ozone. The optimum sorbent is a mixture of activated charcoal and sulfite on molecular sieve. To ensure high collection efficiency over long-term field operation, two annular diffusion denuders are combined in series. The first half of the first denuder is filled with Na(2)SO(3) on molecular sieve (23 cm long layer) while the second half of the first denuder and the whole second denuder are filled with activated charcoal (the total length of the charcoal section is 67 cm). At a flow rate of 16.6 L min(-1), the collection efficiency of organic gaseous compounds and atmospheric oxidants in the annular diffusion denuder is better than 95%. Only small losses of aerosol particles (<3.6% in number concentration) were observed in the size range 0.12-2.26 μm. The annular diffusion denuder is compatible with the collection of aerosols on 47-mm diameter quartz fiber filters at a flow rate of 16.6 L min(-1). The use of this denuder enables one to sample carbonaceous aerosols on filters without positive sampling artefacts from volatile organic compounds and interferences from atmospheric oxidants. The annular diffusion denuder has been applied successfully for the sampling of carbonaceous aerosols during field campaigns of typically 1 month each at urban and forested sites in Europe.

Pressurised liquid extraction of ketones of polycyclic aromatic hydrocarbons from soil.

Pressurised liquid extraction (PLE) was used in the extraction of three ketones of polycyclic aromatic hydrocarbons from the sample of a soil highly contaminated with polycyclic polyaromatic compounds. The choice of solvent was the only factor that considerably influenced the extraction efficiency of PLE under the conditions recommended in Method 3545A promulgated by the United States Environmental Protection Agency. The dichloromethane-ethanol solvent mixture was found to be the most efficient solvent. PLE using this mixture provided better recoveries of all analysed ketones relative to Soxhlet extraction.

Embryonic Toxicity of Nanoparticles

Applications of nanoparticles (NP) in medicine, industry and other branches of human activities undoubtedly contribute to technology development and well-being. However, as NP are very small units in a wide range of materials, there is a lack of information related to possible side effects potentially affecting the health of organisms. There is increasing experimental interest in the determination of environmental effects on humans exposed to NP. Most such experimental studies focus on adult populations or adult experimental animals. However, embryos can be more sensitive to pollutants and environmental impacts in some species. Therefore, some investigations dealing particularly with the effects of NP on embryonic development have appeared recently and this issue is becoming of great concern. The aim of this review is to summarize the knowledge on the effects of various nanomaterials on embryonic development. A comprehensive collection of significant experimental nanotoxicity data is presented, which also indicate how the toxic effect of NP can be mediated and modulated with respect to possible effective protection strategies.

A portable device for fast analysis of explosives in the environment

A novel portable device for fast and sensitive analysis of explosives in environmental samples is presented. The developed system consists of miniaturized microcolumn liquid chromatograph, photolytic converter and chemiluminescence detector. The device is able to determine selectively nitramine- and nitroester- and most of nitroaromates-based explosives as well as inorganic nitrates at trace concentrations in water or soil extracts in less than 8 min. The device allows to analyze various environmental samples such as soils or water materials without previous preconcentration. Because of internal power supply, the device ensures 12h of continuous operation. Limits of detection of compounds of interest are in the range of concentrations from 5.0 × 10(-9)M to 8.0 × 10(-5)M for a signal-to-noise ratio of 3. Limits of quantification are in the range of concentrations from 1.7 × 10(-8)M to 2.7 × 10(-4)M for a signal-to-noise ratio of 10. The repeatability of the method (RSD=2.9-5.6%) was determined by repeated injections (n=10) of the standard samples during 4h.

Photo-induced flow-injection determination of nitrate in water

A sensitive flow-injection method for the chemiluminescent determination of ultra-low concentration of nitrate in water is presented. Nitrate is on-line photolytically converted to peroxynitrite by absorption of UV light inside of 60 mm long quartz capillary (i.d. 530 µm, o.d. 720 µm). Peroxynitrite is subsequently determined by the chemiluminescent reaction with luminol. The detection limit of nitrate is 7 × 10−10 M (S/N = 3). The linear range of the method is 2 × 10−9–1 × 10−5 M nitrate. The interference of nitrite is eliminated by its conversion to nitrogen after mixing of sample with a solution of sulfamidic acid. Other common anions do not interfere. The interference of cations is eliminated by passing the sample through a cation-exchange column. The FIA procedure allows analysing of 15 samples per hour. The method was applied to the determination of nitrate in various real water samples. The results are in good agreement with a reference ion chromatographic method.

Antimicrobial properties and chemical composition of liquid and gaseous phases of essential oils

The antimicrobial properties of fifteen essential oils (EOs) tested on seventeen microorganisms were determined using the vapour-agar contact method. The most effective EOs (i.e. Lavandula angustifolia, Cymbopogon nardus, Citrus aurantifolia, Juniperus communis, Myrtus communis and Cinnamomum zeylanicum), whose volatile components afforded the best antimicrobial properties, were selected for a detailed study of chemical composition. All these six EOs contained one to three main components that presented 67–91 mass % of total mass of a corresponding essential oil. The amount of other components was much lower (less than 5 mass %). The volatile components of Lavandula angustifolia exhibited the most effective antimicrobial properties because they completely inhibited the tested bacteria and fungi within 3 days and 1 week, respectively. The components of Lavandula angustifolia with the highest concentration in the gaseous phase were linalool (99.0 ppmv), eucalyptol (44.9 ppmv), linalyl acetate (25.9 ppmv), myrcene (22.2 ppmv), β-trans-ocimene (19.7 ppmv), camphor (16.7 ppmv) and limonene (14.9 ppmv).

Analysis of water-soluble fraction of metals in atmospheric aerosols using aerosol counterflow two-jets unit and chemiluminescent detection

A new analytical system for a semi-continuous analysis of water-soluble fraction of particulate metals is described. The system combines the continuous sampling of atmospheric aerosols into deionized water using the Aerosol Counterflow Two-Jets Unit and on-line chemiluminescent detection of water soluble fraction of metals in collected aerosols. The potential of analytical system was studied using Fe3+, Cu2+ and Co2+ as model metals in atmospheric aerosols. The detection limits of particulate Fe3+, Cu2+ and Co2+ (S/N = 3) are 24, 41 and 0.4 ng m−3, respectively. The presented set-up allows the determination of concentration of water-soluble fraction of particulate metals in ‘real time’ with time resolution of 30 min. The system is sufficiently robust for the field application. The method has been applied to the measurement of selected metals in urban TSP (Total Suspended Particles) aerosols in Brno in the Czech Republic. The concentrations of particulate water-soluble Fe3+, Cu2+ and Co2+ were found in the range of 35 to 290, 42 to 462 and 0.5 to 9 ng m−3, respectively.