History effect of light and temperature on monoterpenoid emissions from Fagus sylvatica L.

Monoterpenoid emissions from Fagus sylvatica L. trees have been measured at light- and temperature-controlled conditions in a growth chamber, using Proton Transfer Reaction Mass Spectrometry (PTR-MS) and the dynamic branch enclosure technique.De novo synthesized monoterpenoid Standard Emission Factors, obtained by applying the G97 algorithm (Guenther, 1997), varied between 2 and 32 μg g_DW^?1 h^?1 and showed a strong decline in late August and September, probably due to senescence.The response of monoterpenoid emissions to temperature variations at a constant daily light pattern could be well reproduced with a modified version of the MEGAN algorithm (Guenther et al., 2006), with a typical dependence on the average temperature over the past five days.The diurnal emissions at constant temperature showed a typical hysteretic behaviour, which could also be adequately described with the modified MEGAN algorithm by taking into account a dependence on the average light levels experienced by the trees during the past 10–13 h.The impact of the past light and temperature conditions on the monoterpenoid emissions from F. sylvatica L. was found to be much stronger than assumed in previous algorithms.Since our experiments were conducted under low light intensity, future studies should aim at confirming and completing the proposed algorithm updates in sunny conditions and natural environments.     

Headspace solid phase microextraction method for determination of triazine and organophosphorus pesticides in soil

A headspace solid phase microextraction method (HS-SPME) for simultaneous determination of five pesticides belonging to triazine and organophosphorus pesticide groups in soil samples was developed. Microextraction conditions, such as temperature, extraction time and sodium chloride (NaCl) content were investigated and optimized using 100 μ m polydimethyl-siloxane (PDMS) fiber. Detection and quantification were done by gas chromatography-mass spectrometry (GC-MS). Relative standard deviation (RSD) and recovery values for multiple analysis of soil samples fortified at 30 μ g kg^{? 1} of each pesticide were below 13 % and higher than 70 %, respectively. Limits of detection (LOD) for all the compounds studied were less than 3.2 μ g kg^{? 1}. The proposed method was applied in the analysis of some agricultural soil samples.     

Evaluation of oxidation stability of lignite humic substances by DSC induction period measurement

The stability of lignite humic acids and four regenerated humic acids was estimated by employing differential scanning calorimetry. Induction period for the oxidative decomposition of humic matter was calculated from non-isothermal measurements at six different rates of heating. To simulate the gradual evolution history of humic acids, different intensities of oxidation attack by nitric acid on the original lignite was used. Experimental data showed higher stability of natural humic acids in the temperature range where the decomposition step occurred. On the other hand, extrapolation to lower temperatures and calculated kinetic parameters did not correspond to the order observed at higher temperatures. An oscillating trend of calculated parameters of the two proposed parts of stability was observed, which agreed with data concerning regenerated humic acids production. The approach applied in this work represents a rapid and useful method for evaluation of organic matter stability.     

Comparative evaluation of procedures for the determination of PAH in low-volume samples

The aim of this investigation was to evaluate a simplified version of an HPLC method for the determination of PAH in suspended particles collected from small air volumes indoors, outdoors or in personal exposure measurements. The simplification consisted in: (a) collecting PAH by low-volume samplers; (b) extracting PAH ultrasonically; and (c) omitting separation of interfering substances before analysis by HPLC. The results show that the introduction of these modifications affords a considerable reduction in analysis time and solvent expenditure, without affecting the quality of measurement.     

Elimination of ammonia interference in acidimetric determination of sulphur dioxide

Ammonia interference in acidimetric determination of sulphur dioxide can be eliminated by separate determination of ammonia in the same sample and by correction of results. However, with this addition the procedure is no longer simple.To avoid two separate determinations a selective absorption of ammonia from the air stream before it enters the absorbent solution for SO₂ has been considered. Several absorbents used to remove or to collect ammonia for subsequent determination were tested in the laboratory. Whatman No. 1 (or 41) filter papers impregnated with 3% oxalic acid solution in ethanol proved to be the most efficient for ammonia retention without an effect on SO₂. In a comparative testing over 52 days at a permanent sampling station no statistically significant difference was observed between two trains with impregnated filters and a third train where correction for ammonia, separately determined in the same sample, was performed.Regression analysis, however, showed that the results obtained in the third train are more dispersed due to accumulated errors in two analyses at low concentration levels further aggravated by conversion of ammonia to equivalent SO₂ concentrations. The removal of ammonia with impregnated filters gives better precision with less inconvenience and is therefore preferable.     

PAH Levels and Profiles in the Suspended Particulate Matter in Zagreb through Four Seasons

This paper presents the analysis of polycyclic aromatic hydrocarbons (PAHs) measured in all four seasons in suspendedparticulate matter (SPM) collected with a high-volume sampler on one measuring site in the northern part of Zagreb. About 30 samples of SPM were analysed for each season, including workdays and weekends and there were no differences amongst them. The concentrations of all PAHs were highest in winter andlowest in summer. The spring PAH concentrations were lower thanthe autumn ones, as the spring had more sunny and warm days. Theprofiles of PAH/BaP at the measurement sites showed that the mainsource of PAHs in spring and summer was traffic while asubstantial amount of autumn and winter PAHs, besides traffic,came from heating.     

Survey of carbon monoxide concentrations in selected urban microenvironments

Carbon monoxide concentrations were measured in six shops situated in narrow busy streets of the city centre for ten days in winter and ten days in summer and correlated with the measurements simultaneaously performed at an outdoor background reference point. The correlation was significant for four out of six shops in winter, but not in summer. Day-to-day variations seemed to be influenced by gross contamination due to changing weather conditions whereas differences in concentration levels from site to site were strongly influenced by the proximity and density of traffic. The exposure of a pedestrian in winter was in good correlation with background outdoor levels and it was considerably lower than that of a car driver driving though the city.     

Study of personal exposure to airborne respirable particles and carbon monoxide

Simultaneous measurements of CO and respirable particles (RP) at outdoor network stations and of personal exposure in a sample of twelve volunteers were carried out during the winter and summer season of 1980/81 in order to evaluate how well personal exposure can be assessed from outdoor network station data.The results have shown that personal exposure of our subjects to both CO and RP is in best correlation with exposure at home where subjects spend in the average nearly 70% of their time. While personal exposure to CO can hardly be related to outdoor CO levels, personal exposure to RP is in fair agreement with simultaneously measured outdoor concentrations in winter (but not in summer). A large intercept on WAE axis of the WAE/RP relationship indicates that a considerable part of personal exposure to RP should be attributed to particles which are not of indoor origin. This part does not follow the seasonal and day-to-day changes in outdoor RP concentration and causes a negative, but highly significant correlation between WAE/RP ratio and RP.