Effect of SO2 on the reproduction of pea aphids, Acyrthosiphon pisum, and the impact of SO2 and aphids on the growth and yield of peas

Pea aphids feeding from birth to maturity on pea plants (Pisum sativum) exposed to SO(2) concentrations of 50 nl litre(-1) or 80 nl litre(-1) showed a significant 19% increase in the rate of nymph production during the reproductive period, compared to control aphids feeding on plants in charcoal-filtered air. The higher nymph production resulted in a mean 4.6% increase in the intrinsic rate of population increase (rm). In longer term glasshouse fumigation experiments pea aphid populations were, on average, 1.8 times greater on pea plants in ambient air plus 45 nl litre(-1) SO(2) than in ambient air alone. Aphid infestation in ambient air caused a 42% reduction in pea yield and affected most plant parameters adversely. Ambient air plus SO(2) had no direct effect on yield, but, in combination with aphid infestation, a further 10% reduction in yield was recorded.     

Air pollution and agricultural aphid pests. I: Fumigation experiments with SO2 and NO2

A wide range of aphid/host-crop systems was surveyed by means of fumigation experiments in closed chambers for sensitivity to SO(2) and NO(2) at a concentration of 100 nl litre(-1). Aphid performance was measured by the mean relative growth rate (MRGR) of individual aphids. In all cases, except for Acrythosiphon pisum (Harris) on Vicia fabaL., there were increases in the MRGR of the aphids feeding on fumigated plants as compared to clean air controls, both during and post fumigation. The increases in MRGR ranged from 6 to 75%, with the majority falling between 25 and 40%. A. pisum on V. faba showed a consistent negative response, with decreases in MRGR between -9 and -12%. The changes in aohid MRGR were not due to direct effects, as no significant differences in MRGR were observed between fumigated and clean air chambers when aphids were fed on artificial diet sachets during fumigation.     

Responses to ozone of insects feeding on a crop and a weed species

The influence of ozone on insect herbivore growth and population development was investigated. Fumigation of both pea (Pisum sativum L.) and dock (Rumex obtusifolius L.) at a range of O(3) concentrations between 21-206 nl litre(-1) produced changes in mean relative growth rates of the aphids Acyrthosiphon pisum Harris and Aphis rumicis L. of between 24 and -6% relative to controls. However, there was no evidence of a dose-related response to O(3) fumigation and no clear differences in aphid response when fumigated with the plant on prefumigated or previously unfumigated plant material. It is suggested that this may, in part, be due to the presence of NO contamination during O(3) fumigation. However, the MRGR of dock aphids was found to be greater on new compared to old leaves as well as the increase on the new growth and decrease on the old growth of fumigated plants relative to unfumigated controls. The size of egg batches of the chrysomelid beetle Gastrophysa viridula Degeer were found to be larger, survival and productivity of larvae was higher, and the food consumption lower on R. obtusifolius fumigated with 70 nl litre(-1) O(3) compared with unfumigated controls. This meant that these beetle larvae consumed less leaf area per mg of production on fumigated leaves probably because of their better nutritional quality and/or reduced leaf defences. However, the rate of development of larvae was similar on fumigated and control plants.     

The effects of sulphur dioxide on the parasitism of the rust fungus Uromyces viciae-fabae on Vicia faba

Vicia faba cv. Aguadulce was grown in fumigation chambers ventilated with filtered air or air containing sulphur dioxide (SO(2)) at controlled concentrations, and inoculated with the rust fungus Uromyces viciae-fabae. The influence of the pollutant was rated in terms of production of uredia and dehiscent urediospores. Exposures to SO(2) levels around 70-90 nl litre(-1) enhanced uredia density. Pre-inoculation fumigations at 70-86 nl litre(-1) increased uredia density, whilst post-inoculation fumigations stimulated urediospore production. Lower concentrations increased diffusion resistance of the host plant and slightly increased uredia density. Concentrations between 100 and 130 nl litre(-1) were somewhat inhibitory for the parasite, even in the absence of any visible damage symptoms on the host. Total sulphur accumulation in leaf tissue was reduced by the presence of the fungal infection. Growing under SO(2) pollution neither decreased germination ability nor modified morphological parameters of the urediospores. However, elongation of the germination tube of spores coming from filtered air was adversely affected by the pollutant.     

Effects of sulphur dioxide and nitrogen dioxide, singly and in mixture, on the macroscopic growth of three birch clones

An investigation of some aspects of the effects of low concentrations of the gases, sulphur dioxide and nitrogen dioxide, singly and in mixture, was made on the growth of three birch clones, two of Betula pendula Roth. (silver birch) and one of Betula pubescens Ehr. (downy birch). Comparative measurements of the growth form and dry mass increment were made over one year in glasshouses supplied with charcoal-filtered ambient air, and SO(2) and NO(2), singly or in mixture, at mean concentrations of 62 ppb (nl litre (-1)) of one or both gases. The main effects were found in those plants that were fumigated with SO(2) singly, and SO(2) and NO(2) together. Both treatments induced premature leaf loss and reduction in mass, especially of roots, the effects increasing over time. The heights and initial leaf areas were maintained, apparently at the expense of other parameters. NO(2), if present singly, had little or no effect, but it tended to enhance the damaging effect of SO(2) when the two were applied together. The different clones showed different degrees of response to the pollutants, but these differences became less marked during the second season of fumigation. The effects found are discussed in relation to the annual growth of trees, particularly birch.     

Interactions between Sitka spruce, the green spruce aphid, sulphur dioxide pollution and drought

Sitka spruce trees, with and without the aphid Elatobium abietinum and/or drought treatment, were subjected to 25 nl litre(-1) of sulphur dioxide over a 2-month period. Aphids became three times as abundant on the fumigated trees if they were well watered and twice as abundant on trees from which water was withheld, compared with unfumigated controls. Growth parameters of the trees were little affected by pollution alone, but were substantially reduced by either aphids or drought. There was a significant interaction between SO(2) and aphids in a further reduction of both leader extension and root weight. Root weight was also reduced by 24% more than expected from the additive effects of the combined SO(2) and drought treatment.     

Combined use of open-air and indoor fumigation systems to study effects of SO2 on leaching processes in Scots pine litter

Both an open-air fumigation system and a laboratory-based system were used to expose decomposing Scots pine (Pinus sylvestris L.) needles to controlled concentrations of SO(2) (arithmetic mean 相似文献   

Effects of air pollution on rice yield in the Pakistan Punjab

A study using open-top chambers ventilated with ambient or charcoal filtered air in the vicinity of Lahore, Pakistan demonstrated reductions of 42% and 37% in the grain yield of two cultivars of rice (Oryza sativa L.). This yield reduction was primarily due to the reduction in mean panicle number per plant, although significant effects of filtration on 1000 grain weight and the number of filled grains per panicle were also detected. The 6-h daily mean O(3) concentrations were only 10-20 nl litre(-1) during the monsoon season, but increased to 30-55 nl litre(-1) later in the growing season, while the mean NO(2) concentration during the experiment was 12 nl litre(-1). On the basis of experience in North America and Japan, the reductions in yield in the present study are substantially greater than might be predicted. The reasons for this discrepancy are discussed, together with the implications for effects on rice yield in other regions of south and south-east Asia.     

Peroxidative processes induced in bean leaves by fumigation with sulphur dioxide

Bean plants have been fumigated for 1 h with 300 or 1000 nl litre(-1) SO(2). Dependent on the SO(2) concentration, we observed an evolution of ethane the leaves. Even with 1000 nl litre(-1) SO(2) the evolution lasted for only 4 h. Pretreatment of single leaves with the radical scavenger ethoxyquin prevented this SO(2)-induced ethane formation. Another indication for the initiation of radicalic peroxidative processes by SO(2) was obtained by the manipulation of the endogenous antioxidants vitamin C and glutathione. An increase of both compounds by application of precursors of both biosynthetic pathways could completely suppress peroxidative ethane evolution. We also found a very good quantitative correlation between endogenous glutathione and ethane formation after SO(2) treatment. During these peroxidative processes, several cell components like fatty acids, chlorophylls, carotenoids and vitamin C were decreased. Based on our results, a mechanism for SO(2) induction of radical reactions leading to peroxidation and the role of endogenous antioxidants are discussed.     

Effects of air filtration at small SO2 and NO2 concentrations on the yield of barley

Two cultivars of Igri and Gerbel winter barley Horteum vulgare L. were grown in open-top chambers in filtered and unfiltered air at a site with approximately 10 nl litre(-1) SO2 and 12 nl litre(-1) NO2 (seasonal mean). The experiment ran for three consecutive seasons 1982-1983, 1983-1984, 1984-1985, and significant effects of filtration were observed for each crop. In years 1982-1983 and 1984-1985, the crops in unfiltered air yielded larger grain dry matter, 9% in 1982-1983, and 8% in 1984-1985. For both crops, the differences were statistically significant at the 5% level. Differences were also observed for the remaining above-ground dry matter, and these were consistent in direction in each year but statistically significant only in 1984-1985. In both growing seasons (1982-1983 and 1984-1985), there were no major pest infestations and no long-term water stress or photochemical ozone episodes. In the remaining experiment (1983-1984) similar air concentrations of SO2 and NO2 produced effects of the opposite sign to those observed in 1982-1983 and 1984-1985. Significant reductions in grain yield (13%) were obtained in unfiltered air. The only major environmental difference for the 1983-1984 crop was a notable dry period in May and June 1984 with marked water stress in the crop, requiring irrigation. These results suggest that the relationship between yield and pollutant concentration may be confounded by additional stresses, many of which are a common component of the growing season for major crops.     

Effects of elevated CO2, nitrogen supply and tropospheric ozone on spring wheat-II. Nutrients (N, P, K, S, Ca, Mg, Fe, Mn, Zn)

CO(2) enrichment is expected to alter leaf demand for nitrogen and phosphorus in plant species with C(3) carbon dioxide fixation pathway, thus possibly causing nutrient imbalances in the tissues and disturbance of distribution and redistribution patterns within the plants. To test the influence of CO(2) enrichment and elevated tropospheric ozone in combination with different nitrogen supply, spring wheat (Tritium aestivum L. cv. Minaret) was exposed to three levels of CO(2) (361, 523, and 639 microl litre(-1), 24 h mean from sowing to final harvest), two levels of ozone (28.4 and 51.3 nl litre(-1)) and two levels of nitrogen supply (150 and 270 kg ha(-1)) in a full-factorial design in open-top field chambers. Additional fertilization experiments (120, 210, and 330 kg N ha(-1)) were carried out at low and high CO(2) levels. Macronutrients (N, P, K, S, Ca, Mg) and three micronutrients (Mn, Fe, Zn) were analysed in samples obtained at three different developmental stages: beginning of shoot elongation, anthesis, and ripening. At each harvest, plant samples were separated into different organs (green and senescent leaves, stem sections, ears, grains). According to analyses of tissue concentrations at the beginning of shoot elongation, the plants were sufficiently equipped with nutrients. Elevated ozone levels neither affected tissue concentrations nor shoot uptake of the nutrients. CO(2) and nitrogen treatments affected nutrient uptake, distribution and redistribution in a complex manner. CO(2) enrichment increased nitrogen-use efficiency and caused a lower demand for nitrogen in green tissues which was reflected in a decrease of critical nitrogen concentrations, lower leaf nitrogen concentrations and lower nitrogen pools in the leaves. Since grain nitrogen uptake during grain filling depended completely on redistribution from vegetative pools in green tissues, grain nitrogen concentrations fell considerably with severe implications for grain quality. Ca, S, Mg and Zn in green tissues were influenced by CO(2) enrichment in a similar manner to nitrogen. Phosphorus concentrations in green tissues, on the other hand, were not, or only slightly, affected by elevated CO(2). In stems, 'dilution' of all nutrients except manganese was observed, caused by the huge accumulation of water soluble carbohydrates, mainly fructans, in these tissues under CO(2) enrichment. Whole shoot uptake was either remarkably increased (K, Mn, P, Mg), nearly unaffected (N, S, Fe, Zn) or decreased (Ca) under CO(2) enrichment. Thus, nutrient cycling in plant-soil systems is expected to be altered under CO(2) enrichment.     

Detection of sulphite in plants

Artificially SO(2)-fumigated plant material was investigated for its sulphite content. Experiments with moderate concentrations of SO(2) (0.15-0.45 mg m(-3) lasting for 3 weeks, showed no detectable amounts of sulphite present in peas. Considering the detection limit of the method, this indicates that the steady state level in plant tissues is below 4 x 10(-5)M sulphite. Only in pea plants exposed to very high SO(2)-doses of 2.6-26mg m(-3) for 12-48 h, was sulphite recorded. We conclude from our results that sulphite dioxide, taken up by pea plants, is very effectively removed by enzymic and non-enzymic processes, and this 'detoxification' prevents accumulation of sulphite in the plant tissue, and so only very small amounts of sulphite are to be expected in SO(2)-damaged plant material. The possible role of very low sulphite concentrations in plant tissues is discussed.     

Responses of bean (Phaseolus vulgaris L. cv. Pros) to chronic ozone exposure at two levels of atmospheric ammonia

Plants of bean (Phaseolus vulgaris cv. Pros) were exposed to a range of O3 concentrations up to 70 nl litre(-1) for 9 h day(-1) in the presence (45 nl litre(-1)) and absence (21 nl litre(-1)) of enhanced NH3 in 12 open-top chambers. Treatment effects on visible injury, growth and yield were assessed after 49 (intermediate harvest) and 62 days of exposure (final harvest). The proportion of leaves with visible injury at final harvest increased with increasing concentrations of O3. Enhanced NH3 did not cause any symptoms and did not affect injury by O3. The estimated seasonal mean concentration corresponding with 5% injury was circa 23 nl litre(-1) O3. Biomass production and green pod yield decreased with increasing concentrations of O3 and were generally stimulated by enhanced NH3 at both harvests. Adverse effects of O3 on biomass and pod yield did not depend on the NH3 level. Relative yield response to increasing 9-h daily mean O3 concentrations was nonlinear and yield losses of 5 and 10% were calculated to occur at seasonal daytime mean concentrations of 27 and 33 nl litre(-1) O3, respectively. Linear regression showed that the Accumulated exposures Over a Threshold of 30 (AOT30) and 40 nl litre(-1) (AOT40) O3 performed equally well. The estimated accumulated O3 exposures corresponding with a yield loss of 5% were 1600 nl litre(-1) h for AOT30 and 400 nl litre(-1) h for AOT40. The results are discussed in relation to the long-term critical level that is used as a guideline to protect crops against adverse effects by O3.     

Influence of ozone and ethylenediurea (EDU) on growth and yield of bean (Phaseolus vulgaris L.) in open-top field chambers

Greenhouse and ambient air experiments have shown ethylene diurea (EDU) to be a strong and specific protective suppressant of ozone injury in plants. To examine how EDU affects plant responses to various ozone (O(3)) levels under controlled field conditions, Phaseolus vulgaris L. cv. Lit was treated with 150 ppm EDU every 14 days and exposed in open-top chambers to charcoal-filtered air (CF), nonfiltered air (NF) or two cf treatments with ozone added. The ozone treatments were proportional additions of one (CF1) and two (CF2) times ambient ozone levels. The mean ozone concentrations in the CF, NF, CF1 and CF2 treatments were 0.98, 14.1, 14.98 and 31.56 nl litre(-1). A two-way split plot ANOVA revealed that shoot dry weight was significantly reduced by ozone. EDU treatment was highly significant for leaf dry weight, root dry weight and shoot dry weight, but not for pod dry weight; leading to a higher biomass of EDU-treated plants. Ozone/EDU interactions were significant for root weight only, indicating that EDU reduced growth suppression by ozone. These results show that EDU action on plant biomass could be interpreted as a delay in senescence since EDU-treated plants showed a significant decreased biomass loss even in the CF treatment.     

Effects of acidic gases and mists on the reproductive capability of three fern species

The effects of exposure to 40 nl litre(-1) SO2 + 40 nl litre(-1) NO2 on the reproductive biology of Polypodium interjectum (Shivas), Dryopteris affinis (Lowe) Fraser-Jenkins and Phyllitis scolopendrium (L.) Newman were investigated after 14 weeks exposure in a closed chamber fumigation system. The numbers of sori per pinna were reduced in response to SO2 and NO2 for D. affinis but were unaffected for the other species. Numbers of sporangia in sori and spore viability were reduced in P. interjectum and P. scolopendrium but not in D. affinis in response to the SO2 and NO2 treatment. Spore size was not affected by the pollution treatment. A separate experiment tested viabilities of spores collected from the three species in response to daily spraying with simulated mists at pHs of 2.5, 3.5, 4.5 and 5.6. For all three species, there was little or no spore germination in the pH 2.5 treatment and significantly reduced germination in response to the pH 3.5 as compared to the pH 4.5 and pH 5.6 treatments.     

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%.     

Air pollution and agricultural aphid pests. II chamber filtration experiments

The responses of four major aphid pest species feeding on three major crops were studied in a series of experimental chambers on the roof of Imperial College in South Kensington, London. The experimental chambers were continually circulated with air which had been subjected to a variety of filtration treatments. In the first series of experiments there were three chambers subject to ambient air, charcoal-filtered air, and charcoal plus 'Purafil'-filtered air; in the subsequent experiments there were four chambers, a charcoal plus 'Purafil' plus charcoal treatment being added. These treatments provided a range of concentrations and mixtures of the ambient gases present at the site. The growth rate of aphids was measured both during filtration and post-filtration, the plants being exposed from sowing for either 42 or 84 days. In all cases there were significant effects on aphid performance which seemed to be most strongly linked to absolute and relative NO concentrations. The pattern of responses by the aphids accorded extremely well with those observed in closed-chamber fumigation experiments with stimulation of performance in relatively polluted air in all cases except Acyrthosiphon pisum (Harris) feeding on Vicia faba L. where the opposite effect was recorded.     

Dynamics of biomass partitioning in field-grown radish varieties, treated with ethylenediurea

During the growing season of 1990, five staggered crops of radish (Raphanus sativus L.) were grown in the field, using the cultivars 'Cherry Belle', 'Red Prince', and 'Red Devil B'. Half of the plants received a soil drench (100 ml plant(-1); 100 mg litre(-1) of ethylenediurea (EDU) once, early in plant development. Destructive harvests were carried out at 2-day intervals during vegetative development. Non-linear growth kinetics, derived from Richards' function, were fitted to the dry weight data of the total plant, main organs (shoot and hypocotyl) and to the dry weight ratio between below-ground and above-ground organs. Estimating the parameters of these non-linear functions and testing their differences between EDU-treated and untreated plants unveiled biologically meaningful information on the impact of different levels of ambient ozone (O(3)) during the growth periods. The modified function which was applied to the data of biomass partitioning between the major plant parts was more powerful in detecting transient alterations in assimilate allocation compared to the growth dynamics of individual plant organs. At low levels of O(3), biomass partitioning towards the below-ground sink organs was slightly delayed and finally restricted in EDU-treated plants. When ambient O(3) reached moderate levels, which did not cause visible foliar injury, assimilate partitioning between organs was only insignificantly altered during early growth when EDU-treatments were compared. As growth progressed, however, less assimilates were allocated towards the hypocotyl and roots in the plants not protected by EDU. This pattern was similar in all cultivars tested, but was smallest in 'Cherry Belle', which is known to be sensitive to O(3) with respect to foliar injury. During the 15- to 19-day periods of rapid growth, the O(3)-exposure >80 nl litre(-1) ranged from 0.015 to 0.209 microl litre(-1) O(3) h, which corresponds to 7 h d(-1) mean values between 40 and 50 nl litre(-1) O(3), confirming that ambient ozone did not exceed a moderate level in this study.     

Limited compensation of ozone stress by potassium in Norway spruce

The effects of potassium fertilization and ozone stress were investigated in a clone of Picea abies (L.) Karst, by studies of the uptake of CO(2) by the crowns, the element content, on leaching of the youngest needles, and the longevity of the needles. All plants were exposed to 0.075 microl litre(-1) SO(2) from January to April 1986. The average ozone concentrations applied during the subsequent growing season (May-December) were 0, 0.027, 0.050 and 0.100 microl litre(-1). Half of the trees received liquid fertilizer applications from April to July 1986. CO(2) uptake by the crowns was significantly reduced in non-fertilized plants at ozone doses of 100-200 microl litre(-1) h, whereas similar reductions were recorded in fertilized plants only above an ozone dose of 300 microl litre(-1) h. Independent of the fertilization, however, the concentrations of calcium, magnesium and nitrogen in the needles increased in parallel with the ozone dose, whilst potassium, phosphorus and sulphur showed little response to ozone. In both nutrient regimes, the diffusive loss of elements from chloroform-washed needles was similar and tended to be reduced at the highest ozone concentration, when relating the leachate to the corresponding element content in the needles. Needles formed in the highest ozone treatment were significantly shed during the succeeding year, regardless of the nutrient supply. It appears that increased potassium supply has little compensating effect on ozone stress in spruce.     

Injury and physiological responses of Larrea tridentata (DC) Coville exposed in situ to sulphur dioxide

The response of shrubs of Larrea tridentata (DEC) Coville (creosotebush) exposed to sulphur dioxide (SO(2)) was evaluated using in situ plants of the Majove Desert. Larrea was exposed to acute levels of 0.3 to 2.0 microl litre(-1) SO(2) for periods up to 13 days using field chambers or an open-air fumigation system. Plants exposed in the spring exhibited considerable leaf injury (necrosis and defoliation) when exposed to 2.0 microl litre(-1) SO(2), and in the autumn had leaf injury when exposed to >0.4microl litre(-1) SO(2). Injured plants had higher transpiration rates, less negative water pressure potentials, and/or lower photosynthetic rates than control plants. It is likely that Larrea would not be injured by the typically low SO(2) concentrations and dry environmental conditions of the Mojave Desert. However, if injury were to occur, it would be accompanied by changes in plant-water relations and photosynthesis, followed by recovery after the SO(2) stress was removed.