Phytophthora infestans's 10-year truce with Holland: a long-term analysis of potato late-blight epidemics in the Netherlands

A sequence of 47 potato late-blight ( Phytophthora infestans ) epidemics in the Netherlands, from 1950 to 1996, was analysed using agronomic and meteorological variables. The intensity of annual epidemics was characterized by an index of disease intensity (DI, 0 = absence of late blight; 4 = severe epidemic). Three periods were identified, with average DIs of 2·9, 0 and 2, respectively. Period I (1950–68) had relatively regular epidemics; period II (1969–78) was virtually blight free; and period III (1979–96) showed large variations in disease intensity. Disease-enhancing factors were number of days with precipitation, and number of hours with temperatures between 10 and 27°C and relative humidity >90% during the growing season. Limiting factors were number of hours with temperatures >27°C, and amount of global radiation. Linear discriminant analysis of DI using the blight status of the previous year and meteorological variables correctly classified up to 40 years out of 47 (87·0%), with five out of the six incorrectly classified years falling in period III. Blight status of the previous year and number of days with precipitation were important discriminating variables.     

Effects of temperature and moisture on disease and fruit body development of Mycosphaerella pinodes on pea (Pisum sativum)

The effects of temperature (5–30°C) and the duration of moisture on the development of ascochyta blight ( Mycosphaerella pinodes ) on pea seedlings, grown under controlled conditions, were investigated. The optimum temperature for monocyclic processes was 20°C. At this temperature, pycnidiospores germinated after 2 h, appressoria formed after 6 h and the germ-tube penetrated the leaf cuticle after 8 h. Disease symptoms were evident after 1 day of incubation and the first pycnidia formed after 3 days. Longer wetting periods were required for disease development and pycnidial formation at non-optimal temperatures. Disease severity and the number of pycnidia formed on leaves increased with temperature from 5 to 20°C, then decreased between 20 and 30°C. Polynomial equations were fitted to predict the stages of infection, incubation, latency and disease development as functions of temperature and duration of moisture. These equations allow comparisons of pathogen spread with plant development and could be incorporated into disease development models used for crop management programmes.     

Induction of systemic resistance to <Emphasis Type="Italic">Exobasidium vexans</Emphasis> in tea through SAR elicitors

The effect of two chemical elicitors (acibenzolar-S-methyl benzo-[1,2,3]- thiadiazole-7-carboxylic acid S-methyl ester [Boost 500SC]) and salicylic acid in inducing resistance in tea plants against blister blight disease caused by Exobasidium vexans Massee, was studied. Treatments with elicitors resulted in reduced severity of blister blight disease in nursery plants on challenge with the pathogen. There was a significant increase in the activities of defense enzymes like phenylalanine ammonia lyase, peroxidase and β-1,3-glucanase on elicitor treatments in tea leaves challenged with the pathogen than on unchallenged leaves. Acibenzolar-S-methyl (ASM) at 0.14% registered the lowest disease severity (25.2%), whereas treatments with salicylic acid were inferior. Under field conditions, the application of ASM at 0.14% resulted in disease protection of 25%. When ASM was applied in alternate rounds with a standard fungicide, the disease protection improved to 46.8%. The importance of incorporating ASM as a component in integrated disease management and also its importance in organic tea cultivation is discussed.     

The effect of phenylamide fungicides on the control of potato late-blight (Phytophthora infestans) in England and Wales from 1978 to 1992

During the period 1978–1992, phenylamide fungicides in co-formulation with the dithiocarbamate fungicide mancozeb were tested for the control of potato late-blight in 51 separate field experiments in England and Wales. Whilst there was a general trend over all the experiments which indicated that foliage blight was less severe where the phenylamide + dithiocarbamate mixture had been used, the benefit was more marked in some than in others. Despite the detection of phenylamide resistance, at some sites the mixture gave better control of foliage blight than the dithiocarbamate alone. At one site where continuous data were available, the additional benefit of the phenylamide compound for control of foliage infection was lost after 1986 coinciding with a rise in phenylamide resistance from 31.7% in 1986 to 81% in 1987. Where foliar blight epidemics occurred, yield responses to fungicide programmes compared with unsprayed controls ranged from 0 to +118.5% with a mean response of +30.2%. This is equivalent to 30.8 and 12.92 t/ha respectively. Standardized yield differences were calculated to allow inter-trial and inter-year comparisons and showed no benefit from the phenylamide fungicide applied at 14-day intervals in 33 out of 38 experiments where foliar blight epidemics occurred. At one site, Cusum analysis of standardized yield differences following treatment with the phenylamide + dithiocarbamate mixture and the dithiocarbamate alone showed a mean benefit from the phenylamide mixture of 2.23 t/ha during the period 1978 to 1986. From 1987 to 1992, the yield benefit dropped to a mean level of 0.68 t/ha a decrease of 69.5%. In experiments where blight was not recorded, fungicide treatments had no deleterious effect on yields. Over all the trials, there was no effect of fungicide treatment on the incidence of tuber blight at harvest.     

Late-blight epidemics on potato in Finland, 1933–2002; increased and earlier occurrence of epidemics associated with climate change and lack of rotation

Changes in the incidence and onset of potato late-blight epidemics in Finland were investigated and compared with possible changes in climate, presence of soil-borne inoculum, and aggressiveness of Phytophthora infestans populations. Datasets were constructed from leaf blight assessments in cultivar trials or fungicide tests carried out at eight experimental sites during the periods 1933–1962 and 1983–2002. Additional data were obtained from late-blight monitoring projects carried out from 1991 to 2002. From 1998 to 2002, the risk of blight outbreak was 17-fold higher compared with the periods 1933–62 and 1983–1997. Simultaneously, the outbreaks of the epidemics began 2–4 weeks earlier. The changes observed were associated with a climate more conducive to blight in the late 1990s. Lack of rotation also advanced blight epidemics by an average of 9 days in 1998–2002, but it did not have this effect in 1992–1997, suggesting that soil borne inoculum may not have been a significant threat to potato until the late 1990s. The aggressiveness of the P. infestans isolates seemed to have only minor effect on the onset of the epidemics after 1991, as the apparent infection rate remained unchanged despite weather conditions more favourable to late blight in the late 1990s. As a consequence of the more frequent and earlier epidemics, the sales of fungicides used against late blight in Finland increased 4-fold from the 1980s to 2002.     

The contribution of ground-level inoculum of Fusarium culmorum to ear blight of winter wheat

In a series of field experiments in eastern England over 5 years, severe ear blight developed only in plots of winter wheat that were inoculated by spraying with conidial suspensions of Fusarium culmorum during anthesis, and in which infection was encouraged by rainfall or mist irrigation. In the absence of artificial inoculation of the ears, F. culmorum caused less extensive ear blight, and only where soil-surface inoculum was available after its application on infested plant material (colonized oat grains) up to 3–4 weeks before anthesis; it then developed most where significant rainfall occurred close to the time of anthesis. A warm, dry period following application of inoculum to the ground in late March contributed to increased infection of grain by F. culmorum , although ear blight was not increased. Ear infection therefore depended on adequate viable inoculum on infested plant debris within the crop, and conditions tending to favour brown foot rot development as well as, subsequently, rainfall and moist conditions during anthesis. These conditions did not occur together naturally during this period. Seedling infection by F. culmorum or Microdochium nivale made no significant contribution to ear blight. Inoculation of ears at anthesis with M. nivale or a locally obtained isolate of F. langsethiae did not produce ear blight symptoms. Possibilities for minimizing the availability of inoculum of F. culmorum and the implications for various options for ear-blight control are discussed.     

Differential susceptibility of barnyard grass (Echinochloa crus-galli var. crus-galli) ecotypes to Exserohilum longirostratum

Ten barnyard grass ( Echinochloa crus-galli var. crus-galli ) ecotypes collected from several locations in Malaysian and Indonesian granaries were tested for variation in their susceptibility to the leaf blight pathogen ( Exserohilum longirostratum ). Four phenological growth stages of the ecotypes were sprayed with E. longirostratum at the rate of 1 × 10⁷ conidia mL⁻¹ under glasshouse conditions. The results of the study showed that plants inoculated with 1 × 10⁷ conidia mL⁻¹ and exposed for 24 h dew periods were severely infected and the percentage dry weight reduction of all ecotypes significantly increased. The 1–2 and 2–3-leaf stage plants were completely killed within 6 days after inoculation. However, susceptibility reactions among the ecotypes were observed at the 4–5-leaf stage, while the 6–7-leaf stage was resistant. The ecotypes, K-02, PK-04, KN-02, CJ-01, and L-01, were the most susceptible ecotypes as indicated by a higher area under disease progress curve value. The apparent disease progress rates for these ecotypes were significantly faster compared to the other ecotypes. The dry weight reduction among the four growth stages was variable. These findings show that the 1–2 and 2–3-leaf stages are the most susceptible, while the 6–7-leaf stage was resistant. This study has confirmed that a variable response to the fungal pathogen occurred within an intraspecific barnyard grass collection.     

Epidemiological importance of Solanum sisymbriifolium, S. nigrum and S. dulcamara as alternative hosts for Phytophthora infestans

Lesions of Phytophthora infestans were found on woody nightshade ( Solanum dulcamara ), black nightshade ( S. nigrum ) and S. sisymbriifolium during a nationwide late blight survey in the Netherlands in 1999 and 2000. Pathogenicity and spore production of P. infestans isolates collected from potato ( S. tuberosum ), S. nigrum , S. dulcamara and S. sisymbriifolium were determined on several host plant species, and oospore formation in naturally infected and inoculated foliage of hosts was quantified. The present population of P. infestans in the Netherlands is pathogenic on S. nigrum , S. dulcamara and S. sisymbriifolium . Oospores were produced in leaves of S. nigrum , S. dulcamara and S. sisymbriifolium following infection with A1 and A2 isolates. Therefore these plant species should be regarded as alternative hosts for the late blight pathogen. In the case of S. nigrum and S. dulcamara infection was a relatively rare event, suggesting that diseased plants do not significantly contribute to the overall late blight disease pressure present in potato-production areas. Oospore production in ageing S. nigrum and S. dulcamara plants in autumn, however, may generate a considerable source of (auto) infections in following years. Considerable numbers of sporangia and oospores were produced on S. sisymbriifolium following infection with P. infestans . Additional field infection data are needed to evaluate the epidemiological consequences of a commercial introduction of S. sisymbriifolium as a potato cyst nematode trap crop.     

Biological control of peach twig blight (Monilinia laxa) with Epicoccum nigrum

Various preparations of spores and mycelium of the antagonist Epicoccum nigrum , alone or in combination with Captan, were applied in four different field trials to peach trees inoculated with Monilinia laxa , the cause of twig blight. Biocontrol obtained after application of E. nigrum was variable each year, depending on the releative disease severity in the first 2–3 weeks after infection and the climatic conditions. In three out of four trials, treatments with E. nigrum were comparable with Captan in reducing disease severity and combinations of E. nigrum and Captan gave a level of disease suppression similar to that given by the antagonist or chemical alone. In the remaining trial, combinations of E. nigrum and Captan were necessary to obtain successful disease suppression.     

Late blight (Phytophthora infestans (Mont) De Bary) development from potato seed-pieces treated with fungicides

Fungicides were applied as seed-piece treatments to control potato late blight, caused by Phytophthora infestans, US8, A2 biotype in controlled environment and field experiments. Efficacy of seed treatments for controlling late blight was examined under three disease development regimes simulated by artifical inoculation; (a) seed-borne infection, (b) transmission of infection resulting from spread during the seed-cutting operation, and (c) infection of foliage by aerial inoculation. Emergence of plants from the seed-borne infection was uniformly low (<40%) in controlled environment and field experiments. In controlled environment experiments some of the plants that emerged from fungicide-treated seed-pieces were infected with late blight. Following exposure of tuber surfaces to P infestans, emergence rates from seed-pieces treated with formulated products that included mancozeb in the formulation were comparable to the untreated and non-inoculated control in controlled environment and field experiments. Plants that emerged from non-inoculated seed-pieces treated with fungicides that contained active ingredients known to be effective against foliar late blight had lower percentage foliar infection after inoculation than the untreated control. Leaves close to the base of the stem had fewer infections than leaves attached at the mid region of the main stem, 14 days after inoculation, in some of the controlled environment studies. In contrast, field experiments conducted under conditions conducive to late blight development showed that none of the seed treatments applied to late blight-free seed-pieces delayed the onset and severity of late blight infection. In potato production areas at risk of early season late blight, seed treatments applied to healthy seed may confer limited protection against late blight between planting and the first scheduled applications of prophylactic foliar fungicides. © 1999 Society of Chemical Industry     

Solar UV-B radiation limits seedborne anthracnose infection and induces physiological and biochemical responses in Lupinus mutabilis

The aim of this study was to test whether solar UV-B radiation and temperature have an effect on infection of lupin seeds by Colletotrichum acutatum. Samples of infected seed were placed in a solar oven and exposed on sunny days for 15, 30, 45, 60, 75, 90 and 120 min. The degree of reduction in disease incidence and seed germination was dependent on the exposure time. Exposure times of 75 min (UV-B 4.41 kJ m⁻², ≈76 °C) and higher reduced incidence from 5% to undetectable levels, but also reduced seed germination by around 10% compared with untreated seed. Therefore, in a second experiment, infected seeds were exposed for 45 or 60 min in the solar oven (UV-B 2.83 or 3.75 kJ m⁻², respectively, ≈76 °C), for 60 min at ambient temperature (UV-B 3.75 kJ m⁻², ≈21 °C) or to dry heat for 60 min at 75 °C. Exposure for 60 min in the solar oven reduced seed infection by 99%, while UV-B-radiated seed at ambient temperature or dry-heat reduced infection by 60% or 32%, respectively. To evaluate the effect of UV-B plus high temperature on seedlings, lupin seed exposed for 45 or 60 min (UV-B 2.83 or 3.75 kJ m⁻², respectively, at ≈76 °C) were grown and physiological and biochemical responses of the seedlings were assessed. Seedlings from exposed seed had higher total concentrations of chlorophyll, protein and peroxidase activity than those grown from unexposed infected seed.     

Evaluation of foliar resistance in potato to Phytophthora infestans based on an international field trial network

During the period 2000–03, local potato cultivars in Estonia, Latvia, Lithuania, Poland and Denmark were tested for foliar resistance to Phytophthora infestans (late blight) in an international field trial network. Four standard cultivars were included in the trials: Sava, Oleva, Danva and Kuras. Primary disease-assessment data were entered into a common database, and parameters from the disease progress curves were calculated and made available on interactive web pages. A regression model, using relative area under disease progress curve (RAUDPC) values for cv. Oleva as a reference, was developed for the estimation of 1–9 scale values, where 1 = most susceptible. Standard deviations for the estimated 1–9 scale values and a nonparametric rank stability analysis of RAUDPC were used to evaluate the stability of resistance of the cultivars. Overall, the results showed stability of resistance for cvs Sava, Oleva and Danva, but not for Kuras. Use of the Internet-based Web-Blight service in this study facilitated comparison of results among countries for the level and stability of resistance. The estimated 1–9 scale values were similar to, or slightly lower than, those from official cultivar lists or from the European Cultivated Potato Database, especially for the more resistant cultivars. Possible reasons for discrepancies from different sources and locations are discussed. It is concluded that RAUPDC and the derived 1–9 scale values are useful for ranking cultivars for resistance to P. infestans , but this information is not detailed enough for use in a decision support system for late blight control.     

Enhanced field control of wheat take-all using cold tolerant isolates of Gaeumannomyces graminis var. graminis and Phialophora sp. (lobed hyphopodia)

Cold tolerant isolates of Gaeumannomyces graminis var. graminis ( Ggg ) and Phialophora sp. (lobed hyphopodia), which produced at least comparable growth rates at 5°C to those of pathogenic G. graminis var. tritici ( Ggt ), were shown to control take-all disease in wheat effectively in 2 years of field experiments in New South Wales, Australia. The addition of oat inoculum of these fungi at the rate of 60 kg/ha to the seeding furrow significantly ( P  ≤ 0.05) reduced disease and increased grain yields by 33–45% compared to the Ggt alone treatment. The use of 30 kg/ha of oat inoculum also significantly ( P  ≤ 0.05) reduced disease and increased grain yields by 21–44%. These high levels of take-all control were obtained consistently from four field experiments on three different soil types with different pHs. A treatment inoculated with Ggg alone showed no disease symptoms and produced grain yields similar to that of untreated wheat. This fungus is, therefore, non-pathogenic to wheat. At high rates of inoculation of Ggg and Phialophora sp. (lobed hyphopodia), 65–80% of tillering wheat plants (GS 32) had root systems colonized by these fungi. In contrast, two Pseudomonas spp. and an isolate each of Ggg and Phialophora sp. (lobed hyphopodia), which did not grow at 5°C, were ineffective in controlling take-all. Take-all assessments during heading (GS 61-83) were highly correlated ( R ²=0.6047, P ≤0.0005) with the relative yield increase or decrease of inoculated treatments compared to the Ggt alone treatment. The use of a Ggg isolate (90/3B) and a Phialophora sp. (lobed hyphopodia) isolate (KY) for take-all control has been patented. These fungi are being developed for commercial use.     

Relationship between leaf emergence and optimum spray timing for leaf blotch (Rhynchosporium secalis) control on winter barley

For wheat, the optimum time to apply fungicide to control disease on a given leaf layer is usually at, or shortly after, full leaf emergence. Data from field experiments on barley were used to investigate whether the same relationship was applicable to control of leaf blotch on barley. Replicated plots of winter barley were sown in the autumns of 1991, 1992 and 1993 at sites in southwest England with high risk of Rhynchosporium secalis infection. Single fungicide treatments at four doses (0·25, 0·5, 0·75 or 1·0 times the label rate) were applied at one of eight different spray times, starting in mid-March in each year, with intervals of 10–11 days between spray timings. Disease was assessed every 10–11 days and area under the disease progress curve (AUDPC) values were used to construct fungicide dose by spray time response surfaces for each of the upper four leaves, for each year. Spray timings shortly before leaf emergence were found to minimize the AUDPC for each year and leaf layer, and also the effective dose (the dose required to achieve a specified level of control), similar to wheat. Fungicide treatments on barley were effective for a longer period before leaf emergence than afterwards, probably because treatments before emergence of the target leaf reduced inoculum production on leaves below. This partly explains why fungicides tend to be applied earlier in the growth of barley compared with wheat.     

Seed transmission of maize downy mildew (Peronosclerospora sorghi) in Nigeria

In an area of Nigeria where downy mildew of maize is present, histological assessment of maize seed revealed the presence of mycelium and oospores of Peronosclerospora sorghi in the kernels. Seed transmission of downy mildew of maize was demonstrated when grain purchased at local markets gave mean seedling infection rates of 12·3% (untreated seeds) and 10·0% (in metalaxyl-treated seeds) within 7 days of emergence, after storage in a desiccator for 30 days. When untreated seeds taken from nubbin ears of systemically infected plants from four states in southern Nigeria were planted at 9 days (17–22% moisture content) and 27 days (9–22% moisture content) after harvest, 20·0% infected seedlings resulted in both trials. Seeds from Borno state in northern Nigeria had 26·6% systemic seedling infection after 9 months of storage at 11% moisture content. When seeds harvested from maize plants inoculated with P. sorghi through silks were examined histologically, hyphae of P. sorghi were observed mostly in the scutellum of the embryo. Transmission of disease to seedlings was observed when the silk-inoculated seeds (9% moisture content) were planted in pots in a greenhouse; however, no disease transmission was observed when such seeds were planted in the field. The epidemiological significance of seed transmission is discussed with particular reference to survival of inoculum and development of epidemics. Also noteworthy is the overall significance of seed transmission in Nigeria, where the major source of seed is that saved by farmers from their grain crop, occasionally supplemented by seed bought from the local market.     

Exploiting host resistance to reduce the use of fungicides to control potato late blight

Field trials in 1996, 1997 and 1998 with six potato cultivars differing in levels of foliar and tuber race-nonspecific resistance to late blight were treated with 100, 50 and 33% of the recommended dose of the fungicide fluazinam at application intervals of 7, 14 and 21 days. Using a mixed inoculum of six or seven indigenous isolates of Phytophthora infestans small potato plots were inoculated via infector plants. A foliar blight model for the relationship between the effects of resistance, fungicide application and disease pressure was developed using multiple regression analysis. Cultivars with a high level of quantitative resistance offered the greatest potential for fungicide reduction. The model showed that the effect of resistance on integrated control increased exponentially with increasing cultivar resistance. Reducing fungicide input by lowering the dose resulted in less foliar disease than extending application intervals. The higher the disease pressure, the greater the risk associated with reducing fungicide input by extension of application intervals. The field resistance of cultivars to tuber blight mainly determined the frequency of tuber infection. Exploiting high foliar resistance to reduce fungicide input carried a high risk when cultivar resistance to tuber blight was low. When field resistance to tuber blight was high, a medium level of resistance in the foliage could be exploited to reduce fungicide dose to c . 50%, provided application was at the right time. At a high level of field resistance to both foliar and tuber blight, application intervals could be extended.     

Effect of pea plant architecture on spatiotemporal epidemic development of ascochyta blight (Mycosphaerella pinodes) in the field

The effect of pea canopy structure on epidemics of Mycosphaerella pinodes was investigated in four spring pea cultivars (Bridge, Obelisque, Solara and Athos) in two field experiments. These cultivars had similar levels of susceptibility to ascochyta blight and presented different architectural features (branching, standing ability and stem height). Stem height ranged from 77 to 95 cm in 1999 and from 72 to 92 cm in 2000, while leaf area index (LAI) ranged from 3·8 to 5·1 in 1999 and from 3·8 to 4·7 in 2000. Internode lengths varied from 4·6 to 6·0 in 1999 and from 3·8 to 4·7 in 2000. Mean distance between nodes in the canopy (MDN) ranged from 12·2 to 15·3 cm in 1999 and from 11·2 to 13·9 cm in 2000. Canopies with different architecture differed in disease progression on stipules and mainly on pods. The levels of disease on stipules and pods were strongly correlated. Moreover, if disease was considered as a function of stipule height up the stem, large differences in vertical disease distribution were observed between cultivars. Three architectural features acted on disease development: cumulative LAI above the node on which disease was assessed (LAIcum) and large MDN favouring disease development, and large internode length reducing disease severity. Modifying LAI distribution and plant organization could be one way to reduce the impact of ascochyta blight, by direct or indirect effects on environmental and dispersal conditions.     

Infection and colonization of melon roots by Monosporascus cannonballus in two cropping seasons in Arizona and California

Although canopy collapse of melons (one of the above-ground symptoms of vine decline caused by Monosporascus cannonballus ) occurred late in the growing season, the onset of root infection occurred much earlier. In three early winter-spring and two late winter-spring crops, the onset of root infection occurred 47–65 and 35–36 days after planting, respectively. In contrast, in four summer-autumn crops, the onset of root infection occurred within 9–17 days after planting. Vine decline occurred commonly in winter-spring crops, but did not occur in any of the summer-autumn crops. Following the onset of root infection, the percentage of plants infected increased at rates of 0·031–0·036 and 0·038–0·070 per unit per day for winter-spring and summer-autumn crops, respectively, based on the monomolecular disease progress model. Root lesions were first observed 14–42 days after the onset of infection in winter-spring crops, and 14–28 days after the onset of infection in summer-autumn crops. Pathogen reproduction occurred primarily at the end of each growing season.     

Evaluation and analysis of reduction of late blight disease in a diploid potato progeny

The rate of late blight disease was analysed for individuals of a diploid Solanum phureja – Solanum tuberosum dihaploid hybrid population (PD), using three different assessment techniques, in the laboratory, screenhouse, and field. These hybrids expressed low disease rates in the field, comparable to resistance based on intact R genes. However, none of the parents of PD expressed any R genes and the pattern of segregation within the PD population was not indicative of R-gene inheritance. The foliage (or leaflet) area diseased had the largest broad-sense heritability of all criteria analysed, in all tests performed. In the field evaluations, the PD population showed intermediate levels of broad-sense heritability for foliage area diseased, relative to the much larger heritability detected for the group of controls possessing R genes. Resistance in the field of the PD hybrids had very little genotype-environment (G × E) interaction, indicating stability of its expression. All genotypes without R genes exhibited heritable, reduced rates of late blight disease in the field, but they were susceptible with low heritability in screenhouse and laboratory tests. This differential expression of disease indicates that the plants' indirect response to unknown environmental stress in the field may have been measured. The value of the PD hybrids for breeding of late blight resistant potato and the use of the disease rate data for detection of the underlying quantitative trait loci are discussed.     

Effects of sunlight exposure on grapevine powdery mildew development

Natural and artificially induced shade increased grapevine powdery mildew (Erysiphe necator) severity in the vineyard, with foliar disease severity 49 to 75% higher relative to leaves in full sun, depending on the level of natural shading experienced and the individual experiment. Cluster disease severities increased by 20 to 40% relative to those on check vines when ultraviolet (UV) radiation was filtered from sunlight reaching vines in artificial shading experiments. Surface temperatures of leaves in full sunlight averaged 5 to 8°C higher than those in natural shade, and in one experiment, filtering 80% of all wavelengths of solar radiation, including longer wavelengths responsible for heating irradiated tissues, increased disease more than filtering UV alone. In controlled environment experiments, UV-B radiation reduced germination of E. necator conidia and inhibited both colony establishment (hyphal formation and elongation) and maturity (latent period). Inhibitory effects of UV-B radiation were significantly greater at 30°C than at 20 or 25°C. Thus, sunlight appears to inhibit powdery mildew development through at least two mechanisms, i.e., (i) UV radiation's damaging effects on exposed conidia and thalli of the pathogen; and (ii) elevating temperatures of irradiated tissues to a level supraoptimal or inhibitory for pathogen development. Furthermore, these effects are synergistic at temperatures near the upper threshold for disease development.