Effects of vapours of chlorpropham and ethofumesate on wild plant species.

Effects of vapours of two herbicides on plantlets of fourteen wild higher plant species and two bryophytes were screened in fumigation experiments using foliar injury, chlorophyll fluorescence and growth as response parameters. After vaporisation of the herbicides for 48 h, concentrations in the chambers reached 77 micrograms m-3 in the chlorpropham treatments and 184 ng m-3 in the ethofumesate treatments. Despite the higher concentrations of the volatile chlorpropham (vapour pressure, VP: 1.3 mP), plants showed no foliar injury, but vapours of this herbicide caused leaf crinkling in the agriophyte Agrostemma githago. The less volatile ethofumesate (VP: 0.56 mP) caused foliar injury in all higher species, with lowest no observed effect concentrations (NOECs) of 75 ng m-3. Chlorpropham affected growth only in Agrostemma, while ethofumesate reduced growth in one third of the higher plant species. Chlorophyll fluorescence proved to be a less suitable response parameter compared to foliar injury and growth. No adverse effects were observed in mosses, probably due to the slow growth and hence small doses of herbicides taken up. The extent of foliar injury due to ethofumesate showed a weak positive relationship to relative growth rates and specific leaf area in the tested higher plant species.     

Effects of sulphur dioxide, hydrogen fluoride and their combination on three Eucalyptus species

The effects of joint action of SO(2) and HF on three Eucalyptus species were studied by exposing them to combinations of < 13, 122 or 271 microg m(-3) of SO(2) and 0.03, 0.39 or 1.05 microg m(-3) of HF in open top chambers for 120 days. HF and SO(2) reduced the area and weight of immature leaves in all three species, but there were few interactive effects on immature leaves. The response of mature leaves to exposure differed among the species, with the greatest effects on E. calophylla and least effects on E. marginata. The interaction of HF + SO2 had no effect on leaf S concentrations in any of the species, but it reduced leaf F concentrations in E. calophylla and E. gomphocephala. HF increased leaf injury in E. calophylla and E. gomphocephala when simultaneously exposed to 271 microg m(-3) of SO(2), but had no effect at 122 microg m(-3), or on E. marginata. The addition of 271 microg m(-3) of SO(2) increased leaf injury when E. gomphocephala was exposed to 0.39 microg m(-3) of HF and when E. calophylla was exposed to 1.05 microg m(-3) of HF, despite reducing the leaf F concentrations. In some cases the interaction of the pollutants may increase susceptibility to visible injury.     

Reduction of net photosynthesis in oats after treatment with low concentrations of ozone

Oats (Avena sativa L. cv Titus) were exposed to low concentrations of O3 in an assimilation chamber system. Net photosynthesis (net CO2 uptake), measured before and after O3 fumigation, showed significantly different responses for leaves of different age. The oldest active leaf was the most sensitive to O3. Net photosynthesis was depressed after 2 h with 0.075 ppm (150 microg m(-3)) O3. For leaves exposed to 0.150 ppm (300 microg m(-3)) O3 for 2 h, net photosynthesis was reduced significantly for 4 h, after which recovery occurred, nearly reaching the preexposure level 19 h after the exposure. Dark respiration was initially more than doubled after exposure to 0.130 ppm (260 microg m(-3)) O3. There was no visible injury after any of the experiments. The results indicate that O3 may cause crop losses through effects on photosynthesis even in Scandinavia, where a typical O3 episode lasts 1 to 2 h, and the concentration seldom exceeds 0.150 ppm.     

Effects of ozone fumigation on epiphytic macrolichens: ultrastructure, CO2 gas exchange and chlorophyll fluorescence

The lichen species Anaptychia ciliaris, Collema nigrescens, Evernia prunastri, Hypogymnia bitteri, Lobaria pulmonaria, Pseudevernia furfuracea and Usnea rigida s.l. were fumigated with site-relevant concentrations (for Central Europe) of ozone over 80 days (180 microg m(-3) during daytime, 80 microg m(-3) during the night). Chlorophyll fluorescence measurements revealed a significant reduction of Fv/Fm after ozone fumigation in five of the species investigated, indicating severe stress on photosystem II due to ozone. The physiological impairment paralleled our fine structural investigations, revealing a significantly higher percentage of collapsed photobiont cells. This indicates that the effects of ambient ozone concentrations under experimental conditions included biophysical and physiological, as well as structural impairment in the lichens studied.     

Indirect effects of air pollutants: Changes in plant/parasite interactions

The impact of air pollutants on plant/parasite-interactions has been investigated. It could be demonstrated that fumigation of Vicia faba L. with 0.15 ppm SO2 (400 microg m(-3)) or 0.2 ppm NO2 (400 microg m(-3)) during 7 days caused changes in plant metabolism which resulted in higher growth rates of the aphid Aphis fabae Scop. feeding on these plants. Fumigation of V. faba with 0.085 ppm O3 during 2 or 3 days, however, caused decreased aphid growth on fumigated plants. That result could be reversed by higher O3 concentrations or through the presence of NOx during O3 fumigation. Ambient air comprising a mixture of pollutant gases had a strong enhancing effect on aphid performance. Thus, the growth of A. fabae on field bean plants was significantly higher in ambient summertime. London air than in charcoal-filtered air. Similarly, the growth of Macrosiphon rosae L. on rose bushes (Rosa sp., cv. Nina Weibull) was improved in ambient summertime Munich air; the increase in growth rate averaged about 20%.     

Single and interactive effects of low levels of O3, SO2 and NO2 on the growth and yield of spring rape

During three consecutive seasons (1987-1989), the effects of low-levels of O3, SO2 and NO2 singly and in all possible combinations (NO2 in 1988 and 1989 only) on growth and yield of potted plants of spring rape (Brassica napus L. var. napus, 'callypso') were investigated by means of factorial fumigation experiments in open-top chambers. Plants were exposed from the early vegetative stage of development until seed harvest, to charcoal-filtered air (CF; control) and CF which was supplemented for 8-h per day (8.00-16.00) with O3, for 16-h per day with NO2 (16.00-8.00) and continuously with SO2. Including the controls, the 24-h daily mean concentrations [microg m(-3)] ranged between 6-44 (O3), 9-88 (SO2) and 10-43 (NO2). The corresponding daily mean concentrations during the time of fumigation were 10-121 and 11-60 microg m(-3) for O3 and NO2, respectively. Single effects of O3 on growth and yield parameters were mostly negative and the magnitude of this effect was dependent on the season. O3 reduced plant dry weight by 11.3-18.6% and yield of seeds by 11.4-26.9%. While medium levels of SO2 stimulated the weight of pods up to 33%, higher concentrations (88 microg m(-3)) caused a decline of yield of 12.3%. From the significant interactive effects which were observed, it could be established that SO2 and NO2 alone mostly acted positively, but that their interaction with each other and especially with O3 was antagonistic, as some of the detrimental effects of O3 were mitigated by these pollutants. An important antagonistic effect between SO2 and O3 or NO2 was observed on yield. While 56 microg m(-3) SO2 increased yield by 9.9% compared to the control treatment, it aggravated the yield loss caused by O3 from -16.18% to -21.4%, and it reduced the yield stimulation caused by NO2 from +11.8% to +4.2%. Leaf area was the only parameter which was negatively affected by all pollutants, their joint action being synergistic.     

Derivation of aquatic predicted no-effect concentration (PNEC) for 2,4-dichlorophenol: comparing native species data with non-native species data

2,4-Dichlorophenol (2,4-DCP) is known as an important chemical intermediate and an environmental endocrine disruptor. There is no paper dealing with the predicted no-effect concentration (PNEC) of 2,4-DCP, mainly due to shortage of chronic and site-specific toxicity data. In the present study, toxicity data was obtained from the tests using six Chinese native aquatic species. The HC₅ (hazardous concentration for 5% of species) was derived based on the constructed species sensitivity distribution (SSD), which was compared with that derived from literature toxicity data of non-native species. For invertebrates, the survival no-observed effect concentrations (NOECs) were 0.05 and 1.00 mg L⁻¹ for Macrobrachium superbum and Corbicula fluminea, respectively. NOECs based on fishes’ growth were 0.10, 0.20 and 0.40 mg L⁻¹ for Mylopharyngodon piceus, Plagiognathops microlepis and Erythroculter ilishaeformis, respectively. For aquatic plant Soirodela polyrhiza, NOEC based on concentration of chlorophyll was 1.00 mg L⁻¹. A final PNEC calculated using the SSD approach with a 50% certainty based on different taxa ranged between 0.008 and 0.045 mg L⁻¹. There is no significant difference between HC₅ derived from native and that from non-native taxa.     

The interaction of SO2 and root-knot nematode on tomato

Intermittent exposure of tomato plants (cv. Pusa Ruby) to SO(2) at 286 microg m(-3) (3 h every heavy third day for 75 days) induced slight chlorosis of leaves. At 571 microg m(-3), considerable chlorosis with browning developed on the foliage. These symptoms were more pronounced and appeared earlier on SO(2)-exposed plants infected with Meloidogyne incognita race 1 (Mi), especially in post- and concomitant-inoculation exposures. Mi and/or SO(2) significantly reduced different parameters of plant growth. Synergistic (positive) interactions between SO(2) and Mi occurred in concomitant- and post-inoculation exposures at 286 and 571 microg m(-3), respectively. In other treatments, an antagonistic (negative) interaction was observed. However, in a few cases, additive effects of SO(2) and Mi were also recorded. Intensity of root-knot (galling) was enhanced at both concentrations of SO(2), while reproduction (egg mass production) of Mi was enhanced in concomitant-inoculation exposures at 286 microg m(-3) and inhibited at 571 micro m(-3). Exposure to SO(2) and/or Mi decreased the number and size of stomata but increased the number and length of trichomes on both the leaf surfaces. Stomatal aperture was significantly wider in the plants exposed to 571 microg SO(2) m(-3) alone and in pre-, post-, and concomitant-inoculation exposures at 286 or 571 microg m(-3). Stomatal aperture was directly related to foliar injury and reductions in growth, yield, and leaf pigments.     

Effects of simultaneous ozone exposure and nitrogen loads on carbohydrate concentrations, biomass, growth, and nutrient concentrations of young beech trees (Fagus sylvatica)

Beech seedlings were grown under different nitrogen fertilisation regimes (0, 20, 40, and 80 kg Nha(-1)yr(-1)) for three years and were fumigated with either charcoal-filtered (F) or ambient air (O3). Nitrogen fertilisation increased leaf necroses, aphid infestations, and nutrient ratios in the leaves (N:P and N:K), as a result of decreased phosphorus and potassium concentrations. For plant growth, biomass accumulation, and starch concentrations, a positive nitrogen effect was found, but only for fertilisations of up to 40 kg Nha(-1) yr(-1). The highest nitrogen load, however, reduced leaf area, leaf water content, growth, biomass accumulation, and starch concentrations, whereas soluble carbohydrate concentrations were enhanced. The ozone fumigation resulted in reduced leaf area, leaf water content, shoot growth, root biomass accumulation, and decreased starch, phosphorus, and potassium concentrations, increasing the N:P and N:K ratios. A combined effect of the two pollutants was detected for the leaf area and the shoot elongation, where ozone fumigation amplified the nitrogen effects.     

Ozone-induced nitrate formation in needles and leaves of Picea abies, Fagus sylvatica and Quercus robur

Much attention has been paid to ozone as a major cause of novel forest decline in Europe. In combination with acidic mist, O(3) has been observed to increase ion leaching. Besides cations lake Mg(2+), Ca(2+), K(+), NH(4)(+), considerable amounts of nitrate were found to be leached by acidic mist from needles of Norway spruce. Controlled fumigation experiments, with 100, 300, and 600 microg O(3)m(-3) over 22 days continuously, have led to a nitrate accumulation of 94.1 +/- 14.8, 119.4 +/- 28.7 and 198.9 +/- 14.9 microg NO(3)(-1) g(-1) FW, respectively, in leaves of Quercus robur. Similar values were found in leaves of Fagus sylvatica and current and previous year needles of Picea abies. Nitrate levels of controls receiving charcoal filtered air were well below 40 microg NO(3)(-) g (-1) FW. Statistically significant elevated nitrate levels were observed after only 48 h of continuous fumigation with 600 microg O(3)m(-3), in all tree species tested, and after 144 h in the 100 microg O(3)m(-3) treatment. In another experiment, trees of Picea abies were kept in two charcoal (C) and two Purafil plus charcoal (P/C) ventilated chambers, and fumigated with O and 500 microg O(3)m(-3) in cabinets of each filter-type in order to eliminate NO(x) from chamber air. After 29 days of continuous ozone fumigation, NO(3)(-) accumulation in needles amounted to 102.0 +/- 37.7 and 137.4 +/- 40.5 microg g(-1) FW in P/C and C-filtered chambers, respectively. Nitrate contents of controls were below 30 microg NO(3)(-)g(-1) FW at the end of the experiment. No significant differences in NO(3)(-) accumulation between filter treatments were observed. Since NO(x) was reduced by more than 95% in the Purafil/charcoal versus the charcoal treatment, NO(3)(-) accumulation in needles can be attributed predominantly to the influence of ozone and not to direct NO(2) uptake of needles by the possible oxidation of NO to NO(2) in the presence of ozone.     

Validation of an ecosystem modelling approach as a tool for ecological effect assessments

In ecotoxicology, derivation of a "safe" environmental concentration is usually achieved by the use of extrapolation factors or by statistical extrapolation from a set of single species toxicity data. These approaches ignore ecological interactions between species in the field. An ecology-based alternative to this pragmatic approach can be ecosystem modelling, which can account for ecological interactions. However, it is largely unexplored how well the predictions of these models quantitatively agree with large-scale experimental studies. Therefore, we evaluated the capacity of a flexible ecosystem model to predict population and ecosystem-level no observed effect concentrations (NOECs) of 7 organic toxicants. These NOECs were compared with population and ecosystem-NOECs observed in 11 micro- and mesocosm studies. For each of the latter studies, the model was customized to account for the specific ecological interactions within these systems and combined with appropriate single-species toxicity data from literature. Population-NOEC predictions were accurate, or at least protective, for 60, and 85% of all considered model populations, respectively. For all 11 studies, a protective ecosystem-NOEC could be derived, being accurate in 7 cases, and conservative in 4 cases. In general, it can be stated that this type of models can serve as an ecology-based alternative to current extrapolation techniques in EEAs and water quality standard setting.     

Foliar injury and leaf diffusive resistance of rice and white bean in response to SO2 and O3, singly and in combination

Plants of rice (Oryza sativa) and white bean (Phaseolus vulgaris) were exposed to 524 microg m(-3) SO2, 392 microg m(-3) O3 and a mixture of both gases, i.e. 524 microg m(-3) SO2 and 392 microg m(-3) O3 to determine the visible foliar injury and leaf diffusive resistance. Response of leaf diffusive resistance was measured on upper and lower surfaces of leaves, i.e. the two unifoliate leaves of bean and the first, second and third primary leaves of rice. The difference in the response may be due to sensitive guard cells causing stomatal closure in the presence of O3, whilst a low concentration of SO2 caused the stomata to open. Thus, SO2 alone is known to decrease, and O3 tends to increase leaf diffusive resistance. However, exposure to both gases increases or decreases the resistance, depending on the species response.     

Effects of nitrogen dioxide pollution on the growth of three fern species

The effects of exposing plants of Dryopteris filix-mas (L.) Schott, Phyllitis scolopendrium (L.) Newman and Polypodium vulgare L. to 60 nl litre(-1) (122 microg m(-3)) NO(2) for 37 weeks were investigated in a closed chamber fumigation system. There was no effect of NO(2) on the numbers of fronds produced for any species at any time during the exposure period. However, at the end of the study, there was a lower dry weight yield of green shoots of D. filix-mas and P. scolopendrium and a higher yield of green shoots of P. vulgare for plants in the NO(2) treatment as compared to control plants. These differences in shoot dry weights were not accompanied by an effect of NO(2) exposure on total plant dry weights.     

Evaluation of municipal sewage treatment systems for pollutant removal efficiency by measuring levels of micropollutants

In order to evaluate the municipal sewage treatment systems used at Harbin municipal sewage treatment plant for their pollutant removal efficiency, raw sewage and effluent samples at different treatment stages from the sewage treatment systems were taken, priority pollutants (PPs) were identified and quantified using gas chromatography-mass spectrometry (GC-MS) and inductively coupled plasma-atomic emission spectrograph (ICP-AES). The test results indicated that there were one hundred and fifty species of organic pollutants identified in the raw sewage sample, and only ten species of PPs in all the sewage samples. The levels of dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), di-n-octyl phthalate (DnOP) in the sewage samples were 0.779-0.111 microg l(-1), 1.977-0.022 microg l(-1), 6.411-2.194 microg l(-1) and 7.152-2.953microg l(-1), respectively, and most of these phthalate esters (PAEs) were removed through anaerobic/aerobic (A/O) process; The levels of alachlor, acetochlor, atrazine were 0.074-0.021 microg l(-1), 0.160-0.096 microg l(-1) and 0.238-0.184 microg l(-1), respectively, and the total removal efficiency of atrazine was poorest through the sewage treatment systems. The levels of Cu, Cr, Se, Hg, Ni and Zn were 0.0030-0.2327 mg l(-1). It is therefore concluded from these results that the sewage treatment systems were efficient in removing most of the organic and inorganic compounds in this study, and so, the discharged effluent could cause little of the secondary pollution of the aquatic environment.     

Ozone episodes in Southern Lower Saxony (FRG) and their impact on the susceptibility of cereals to fungal pathogens

Spring wheat (Triticum aestivum L.) and spring barley (Hordeum vulgare L.) plants were exposed to simulated ozone (O(3)) episodes (7 h day(-1) for 7 days) at maximum concentrations of 120, 180 and 240 microg m(-3) O(3), in comparison to a charcoal-filtered air control. Fumigations were conducted in four closed chambers placed in a climate room. Exposures took place prior to inoculation of the plants with six different facultative leaf pathogens. On wheat, significant enhancement of leaf attack by Septoria nodorum Berk. and S. tritici Rob. ex Desm. appeared, particularly on the older leaves and at the highest level of O(3). The same was true for Gerlachia nivalis W. Gams et E. Müll/Fusarium culmorum (W.F.Sm.) Sacc. on wheat and net blotch (Drechslera teres (Sacc.) Shoem.) or G. nivalis leaf spots on barley. Disease development was promoted both on leaves with and without visible injury following exposure to O(3). Sporulation of the two Septoria species increased at 120 and 180 microg m(-3) O(3); however, it was reduced to the level of the control, if 240 microg m(-3) were applied. No significant effects of predisposition were observed with Bipolaris sorokiniana (Sacc.) Shoem. (syn. Helminthosporium sativum Pamm., King et Bakke), the causal agent of spot blotch, neither on wheat nor on barley. Doses and peak concentrations applied in the experiments were in good agreement with measurements of ambient ozone in Southern Lower Saxony, FRG. Six years' ozone data (1984-1989) revealed the annual occurrence of between 3 and 11 ozone episodes with potentially harmful effects on cereals (three or more consecutive 'ozone days' with 8-h means above 80 microg m(-3)). The frequency of ozone episodes followed by weather periods favourable for infections by facultative pathogens was higher in years with low O(3) pollution than in ozone-rich years, and varied between one and five cases per season. The number of ozone days during the main growing season of cereals (1 April until 31 August) varied from 25 in 1984 to 98 in 1989. However, only 7.9% of ozone days during the 6 years examined were concurrent with weather conditions suitable for fungal infections. It is concluded that the majority of leaf infections in the field happens under low-level concentrations of photooxidants.     

LC-MS-MS analysis and occurrence of octyl- and nonylphenol, their ethoxylates and their carboxylates in Belgian and Italian textile industry, waste water treatment plant effluents and surface waters

Alkylphenols (APs), alkylphenol ethoxylates (APEOs), ethoxycarboxylate metabolites (APECs) and bisphenol A were determined in surface water using solid-phase extraction (SPE) followed by triple-quadrupole LC-MS-MS. APs were separated by LC from APECs using an acetonitrile-water-gradient without the addition of any buffer. Nonylphenol ethoxycarboxylates (NPECs) interfere in the detection of nonylphenols (NPs) when using an acidic mobile phase, because they produce the same MS-MS fragment ions (219>133 and 147). 4n-NP shows the characteristic transition 219>106; it is well suited as internal standard. Nonylphenol ethoxylates NPE(n)Os (n=1-17) were analysed separately in a second run by positive ionization using an ammonium acetate mobile phase. Textile industry discharges, the corresponding wastewater treatment plant (WWTP) effluents and the receiving rivers in Belgium and Italy were analysed. Among the substances investigated, NPE1C and NPE2O exhibited the highest concentrations in the water samples, up to 4.5 microg l(-1) NPE1C in a WWTP effluent and 3.6 microg l(-1) NPE2O in a river. The highest NP levels were found in the receiving rivers (max. 2.5 microg l(-1)). The predicted no-effect concentration (PNEC) for NP of 0.33 microg l(-1) for water species was frequently exceeded in the surface waters investigated, suggesting potential adverse effects to the aquatic environment.     

Effects of ozone, acid mist and soil characteristics on clonal Norway spruce (Picea abies (L.) Karst.)--an introduction to the joint 14 month tree exposure experiment in closed chambers

This paper introduces a series of publications referring to a single 14-month laboratory study testing the hypothesis that the recent decline of Norway spruce (Picea abies (L.) Karst.) at higher elevations of the Bavarian Forest and comparable forests in medium-range mountains and in the calcareous Alps is caused by an interaction of elevated ozone concentrations, acid mist and site-specific soil (nutritional) characteristics. The effect of climatic extremes, a further important factor, was not included as an experimental variable but was considered by testing of the frost resistance of the experimental plants. Results of these individual studies are presented and discussed in the following 14 papers. Plants from six pre-selected clones of 3-year-old Norway spruce (Picea abies (L.) Karst.) were planted in April 1985 in an acidic soil from the Bavarian Forest, or a calcareous soil from the Bavarian Alps. After a transition period, plants were transferred, in July 1986, into four large environmental chambers and exposed for 14 months to an artificial climate and air pollutant regime based on long-term monitoring in the Inner Bavarian Forest. The climatic exposure protocol followed realistic seasonal and diurnal cycles (summer maximum temperature, 26 degrees C; total mean temperature, 9.8 degrees C; winter minimum, -14 degrees C; mean relative humidity, 70%; maximum irradiance, 500 W m(-2); daylength summer maximum, 17 h; winter minimum, 8 h). Plants were fumigated with ozone, generated from pure oxygen (control: annual mean of 50 microg m(-3); pollution treatment: annual mean of 100 microg m(-3) with 68 episodes of 130-360 microg m(-3) lasting 4-24 h), and background concentrations of SO(2) (22 microg m(-3)) and NO(2) (20 microg m(-3)); windspeed was set at a constant 0.6 m s(-1). Plants were additionally exposed to prolonged episodes of misting at pH 5.6 (control) and pH 3.0 (treatment). Simulation of the target climatic and fumigation conditions was highly reliable and reproducible (temperature +/-0.5 degrees C; rh+/-10%; ozone+/-10 microg m(-3);SO(2) and NO(2)+/-15 microg m(-3)).     

Investigations on the photosynthetic system of spruce affected by forest decline and ozone fumigation in closed chambers

Investigations using chlorophyll fluorescence induction kinetics provide the parameters Rfd, L, and Ap to characterize different specifications of the photosynthetic system (PS). The application of ozone, with concentrations between 100 microg m(-3) and 2000 microg m(-3) to spruce in closed chambers yields a reduction of Rfd between 6% and 23% for the current year's needles, which indicates a reduced potential photosynthetic capacity. Further measurements on the current year's needles of spruce of the damage classes S0/S1, S2 and S3 show also a reduction of Rfd of between 7% and 14% in 2 successive years. In addition, the parameter L increases for damaged trees by between 11% and 49%, indicating a change of the chlorophyll content and of the internal energy distribution between PSI and PSII. As no effect of L can be observed with ozone fumigation, it is concluded that the change of some specifications of the PS can be simulated well by ozone fumigation (e.g. Rfd) while other specifications cannot (e.g. L).     

Dose-response studies with the antiozonant ethylenediurea (EDU), applied as a soil drench to two growth substrates, on greenhouse-grown varieties of Phaseolus vulgaris L

To study plant growth and yield effects of the antiozonant ethylenediurea (EDU), which is frequently used for ozone crop loss assessments, dose-response studies were carried out with potted bean plants under greenhouse conditions in winter and spring. Two cultivars of Phaseolus vulgaris L., differing in sensitivity to ozone (O(3)), were grown in unfiltered air on a sandy loam rich in organic matter and on a vermiculite-clay mixture. Four treatments of EDU at concentrations from 300 to 800 mg liter(-1) were given as a soil drench during plant development. Foliar symptoms of EDU phytoxicity were observed at all doses, and plant biomass, particularly pod dry weight, was considerably reduced to increasing doses of EDU. Primary and first trifoliate leaf weight in EDU-treated plants increased as did the number of buds, indicating an extension of vegetative growth and a delay of reproductive processes. 'BBL 290' beans, which are O(3)-sensitive, were injured by EDU more than the O(3)-tolerant 'BBL 274'. The phytotoxic effects of EDU were more pronounced in the synthetic growth substrate than in field soil. In a second experiment, EDU was applied in concentrations from 100 to 400 mg liter(-1) to 'BBL 290' plants, exposed to filtered air or simulated levels of O(3) pollution. In field soil, plant growth and biomass partitioning in filtered air was only slightly altered by EDU, although leaf injury due to EDU occurred. In the vermiculite-clay mix, the biomass of most plant organs, particularly that of roots, was linearly reduced with increasing EDU doses. O(3) did not cause any alteration in plant biomass in field soil-grown and EDU-treated plants. Ozone leaf injury, which affected 67% of primary leaf area in non-treated plants, was completely suppressed by EDU doses as low as 100 mg liter(-1). This indicates that low concentrations of EDU, which do not affect plant growth in field soil, provide sufficient protection from O(3) injury. The need for careful EDU dose-response studies prior to field assessments is emphasized.     

Secondary effects of air pollution: ozone decreases brown rust disease potential in wheat

Young wheat plants were fumigated with 170 microg m(-3) ozone for 3 days, or with 210 microg m(-3) ozone for 7 days, for 7 hours a day. At the end of the fumigation period the plants were inoculated with brown rust (Puccinia recondita f. sp. tritici) uredospores. The development of new uredospore pustules on fumigated and control plants was evaluated as a measure of rust disease potential. The number of pustules on the ozone fumigated plants was greatly reduced in comparison with the number of plants treated with charcoal-filtered air.