Dispersal of Rhynchosporium secalis conidia from infected barley leaves or straw by simulated rain

Simulated rain (mean drop diameter c. 1 or 3 mm) was allowed to fall for 10 – 15 min on to barley leaves or straw infected by Rhynchosporium secalis (leaf blotch). The leaves were supported on a mesh through which run-off water drained and the straw was supported on a rigid surface on which run-off water collected. The numbers of R. secalis conidia and spore-carrying splash droplets collected by horizontal samplers (microscope slides and pieces of photographic film) decreased rapidly with increasing distance from and increasing height above the sources, with half-distances of 2 – 10 cm. Less than 10% of the spores or droplets reached heights of more than 30 cm. Incident drops 3 mm in diameter produced more spore-carrying droplets and dispersed more conidia than did 1 mm drops. The size category of splash droplets with the greatest proportion of the spore-carrying droplets dispersed by 3 mm drops was 200 – 400 μm, whether the source was infected barley leaves or barley straw. For leaves or straw the greatest proportions of spores were carried in droplets > 1000 μm in diameter. The mean diameter of spore-carrying droplets (478 μm) dispersed from free-draining leaves was less than that of droplets from straw plus run-off water (563 μm). However, the leaf source had more spores cm^-2 and the mean number of spores per droplet was greater (113 as opposed to 6·8) than for the straw source.     

Observations on the vapour phase activity of some foliage fungicides

By means of a Botrytis fabae/Vicia faba bio-assay technique it has been demonstrated that phenyl mercury chloride, maneb, mancozeb, dichlo-fluanid and oxythioquinox protect areas of leaf beyond the visible limits of the fungicide deposits. The evidence suggests that the extended areas of protection are due to the release of fungicidal vapours. For a given dose of mancozeb the area of protection was related to the number of conidia of B. fabae dusted on to the leaves and for a given inoculum density it extended with increasing fungicide dose applied in standard drop sizes. When the same dose of fungicide was applied in increasing volumes of water, producing widening areas of deposit, the area of protection also increased. Fungicide deposits aged on leaves for up to 4 weeks continued to release toxic vapours. Contact between the fungicides and leaves or between fungicides and spores was not necessary for the demonstration of the phenomenon since vapours diffused from deposits on glass and inhibited the germination of spores in water droplets placed at a distance from the fungicide source. For a given distance separating the fungicide and the spores inhibition increased with increasing fungicide dose. For a standard fungicide dose, inhibition decreased with increasing distances between the fungicide and the spores. The fungicidal vapours inhibited the germination of spores of test fungi other than B. fabae. The practical implications of these observations are examined in the light of evidence that vapour phase protection can occur on leaves incubated in large cabinets; on leaves pre-incubated at unsaturated humidities; and on leaves incubated in a moving stream of air.     

Dispersal of Septoria nodorum Pycnidiospores by Simulated Rain and Wind

The influence of wind on the splash dispersal of Septoria nodorum pycnidiospores was studied in a raintower/wind tunnel complex with single drops or simulated rain falling on spore suspensions or infected stubble with windspeeds of 1.5 to 4 m/sec. When single drops fell on spore suspensions (depth 0.5 mm, concentration 7.8 × 10⁵ spores/ml) most of the spore-carrying droplets collected on fixed photographic film between 0–4 m downwind (windspeed 3 m/sec) were >200 μm in diameter. However, most spores were carried in droplets with diameter > 1000 μm, 70 % of which carried more than 100 spores. When simulated rain fell on infected stubble most of the spore-carrying droplets collected beyond 1 m downwind (windspeeds 1.4 and 4 m/sec) were <200 μm in diameter and none were >600 μm; most of these droplets carried only one spore. The distribution of splash droplets (with diameter >100 μm) deposited on chromatography paper showed a maximum at 40–50 cm upwind of the target but many more droplets were deposited 20–30 cm downwind, when single drops fell on a spore suspension (concentration 1.2 × 10⁵ spores/ ml) containing fluorescein dye with a windspeed of 2 m/sec; droplets were collected up to 3 m downwind but not more than 70 cm upwind. With a windspeed of 3 m/sec, numbers of sporecarrying droplets and spores collected on film decreased with increasing distance downwind; most were collected within 2 m of the target but some were found up to 4 m. When simulated rain fell on infected stubble, increasing the windspeed from 1.5 to 4 m/sec greatly increased the number of spores deposited more than 1 m downwind. At 1.5 m/sec none were collected beyond 2 m downwind, whereas at 4 m/sec some were collected at 4 m. A few air-borne S. nodorum spores were collected by suction samplers at a height of 40 cm at distances up to 10 m downwind of a target spore suspension on which simulated rain fell.     

Studies on Mechanisms of Splash Dispersal of Spores, using Pseudocercosporella herpotrichoides Spores

Simulated raindrops, 4 or 5 mm in diameter, fell 13 m onto target water films, with Pseudocercosporella herpotrichoides spores incorporated into either drops or targets. Resulting splash droplets were collected on fixed photographic film and numbers of droplets, spore-carrying droplets and spores determined.
The patterns of dispersal of splash droplets, spore-carrying droplets and spores with distance and droplet size were similar for 4 mm and 5 mm incident drops with spores incorporated into either targets or drops. Numbers of droplets, spore-carrying droplets and spores decreased with increasing distance from targets and none were collected at 1 m. However, more spores were dispersed by 5 mm than by 4 mm drops and with spores in targets than with spores in incident drops. Whereas most splash droplets were in the smallest size category (0–100 μm), most spore-carrying droplets were 200–400 μm and most spores were in droplets with diameter greater than 1000 μm. Regressions of square root (number of spores) on droplet diameter were significant (p < 0.001) in all cases. The slopes of regression lines were greater when spores were in targets than when they were in incident drops. Splash droplets were collected up to a height of 70 cm, with most between 15 and 20 cm. The dye experiment showed that most splash droplets contained liquid from both incident drop and target film.     

Local redistribution of fungicides on leaves by water

Local redistribution of various fungicides applied as large or small droplets to detached broad-bean leaflets was examined by laboratory bio-assay with Botrytis fabae and by leaf-printing techniques. The results showed that fungicidal particulate and soluble material will spread in water from the initial deposits and that the protected areas on leaves inoculated after washing were often much greater than on unwashed leaves. The extent of redistribution was related to the inherent toxicity, physical form, duration of weathering and tenacity of the fungicides. The effects of formulating copper oxychloride and zineb fungicides with surface-active agents and adhesives seemed due to differences in the tenacity of the deposits. Results indicated that similar types of redistribution would occur in the field, but the possible importance of the electrokinetic theory of redistribution was not proven.     

Patterns of unobstructed splash dispersal

Unobstructed splash dispersal patterns were measured in the absence of rain over mown grass using a fluorescent tracer, and a colorimetric method was used indoors in still air. When drops fell into a thin horizontal water film 0–1 mm deep, the volume of the incident drops dissipated as splash droplets was similar to the volume splashed from the film, irrespective of the distance of fall of the drops. Drop size, angle of inclination and distance of fall had significant effects on the volume of drops splashed from an inclined surface. The effects of rigidity, inclination and nature of surface were found to be significant when drops impacted onto surfaces with or without a wax covering and either rigidly or loosely supported. When splash- and dry-air-dispersed Lycopodium spores were simultaneously released, many more splashed spores were caught close to the source, but the dispersal gradient of splashed spores was steeper than that of dry-air-dispersed spores. Splash-dispersed spores were caught on slides, cylinders and rotorods but trap efficiency could not be evaluated.     

Dispersal of Septoria nodorum Pycnidiospores by Simulated Raindrops in Still Air

Simulated raindrops, diameter c. 3 or 4 mm, fell 13 m down a raintower onto suspensions of Septoria nodorum pycnidiospores, depth 0.5 mm, or infected straw pieces. Splash droplets were collected on pieces of fixed photographic film. It was estimated that one drop generated c. 300 spore carrying splash droplets, containing c. 6000 spores, from a concentrated spore suspension (6.5 × 10⁵ spores/ml) and c. 25 spore-carrying droplets, containing c. 30 spores, from infected straw pieces (11 × 10⁶ spores/g dry wt). When the target was a spore suspension in water without surfactant, most spore-carrying droplets were in the 200—400 μm size category and most spores were carried in droplets with diameter >1000 μm. When surfactant was added to spore suspensions, most spore-carrying droplets were in the 0–200 μm category and most spores were carried in droplets with diameter 200–400 μm and none in droplets >1000 μm. Regression analyses showed a significant (p < 0.001) relationship between square root (number of spores per droplet) and droplet diameter; the slope of the regression line was greatest when surfactant was added to the spore suspensions. The distribution of splash droplets with distance travelled from the target was better fitted by an exponential model than by power law or Gaussian models. The distributions of spore-carrying droplets and spores with distance were fitted better by an exponential model than by a power law model. Thus regressions of log, (number collected) against distance were all significant (p < 0.01); the slopes of the regression lines were steepest when surfactant was added to the spore suspension. At a distance of 10 cm from target spore suspensions most splash droplets and spore-carrying droplets were collected at height 10–20 cm, with none above 40 cm; at a distance of 20 cm there were most at heights 0–10 cm and 40–50 cm.     

Dispersal of the conidia of Colletotrichum gloeosporioides by rain and the development of anthracnose on onion

The conidia of Colletotrichum gloeosporioides were found to be dispersed during rainfall by wash-off and splash mechanisms. The initiation and development of onion anthracnose was found to depend on the frequency of rainfall and the movement of conidial inoculum during rainfall. Experiments conducted under controlled conditions in the laboratory employing splash and wash-off assemblies showed that impacting incident water drops (splash) and flowing water (wash-off) liberated the conidia from the anthracnose lesions of the onion leaf/peduncle. Peak liberation of conidia occurred with 3 to 5 water drops and most of the conidia were removed from the source within 90 seconds. A possibility of the dispersal of conidia of C. gloeosporioides from soil to lower leaf by splash mechanisms and then from the leaves to the neck of the onion bulb and to the bulb by wash-off mechanisms is indicated.     

Secondary leaf fall of Hevea brasiliensis: meteorological and other factors affecting infection by Colletotrichum gloeosporioides

The lower leaf surface of Hevea brasiliensis was more susceptible to infection by Colletotrichum gloeosporioides than the upper. Few lesions were produced if spore drops on susceptible leaves were allowed to dry. Lesion development after 72 h was quickest at 21 ^oC, slower at 26.5 ^oC and was stopped at 32 ^oC, probably because of bacteria in the inoculation drop. On leaflets aged 7 days from bud-burst, the effective spore dose for 50% of leaflets infected (ED₅₀) after 16 h incubation, was 260 spores and after 46 h, 120 spores/infection droplet; the minimum ED₅₀ for the upper leaf surface was about 4 spores/mm². Leaflets 15 days old, which are normally resistant, were rendered susceptible by abrading the surface with carborundum powder. Spores caught in a Hirst spore trap reached a daily maximum at 23 h, at rates of up to 440 spores/m³ air/h, but fell to low concentrations as the humidity dropped during the daytime, and also during rain. There was some correlation between disease severity and duration of 97–100% relative humidity, and moderate to severe defoliation of clone PB 86 occurred when this reached 13.5 h/day. Rainfall increases infection by prolonging the period of atmospheric saturation and leaf wetness.     

New Insights in the Life Cycle and Epidemics of Phytophthora porri on Leek

White tip, caused by Phytophthora porri, is a devastating disease in the autumn and winter production of leek (Allium porrum) in Europe. This study investigated the disease cycle of P. porri in laboratory and field conditions. Oospores readily germinated in the presence of non‐sterile soil extract at any temperature between 4 and 22°C, with the formation of sporangia which released zoospores. The zoospores survived at least 7 weeks in water at a temperature range of 0 till 24°C. Microscopic examinations revealed that zoospores encysted and germinated on the leek leaf surface and hyphae entered the leaf directly through stomata or by penetrating via appressoria. Oospores were formed in the leaves within 6 days, while sporangia were not produced. By monitoring disease progress in fields with a different cropping history of leek, it could be deduced that P. porri survives in soil for up to 4 years. Disease progress during three consecutive years was correlated with average daily rainfall in the infection period. Disease incidence on leek was reduced when rain splash was excluded by growing the plants in an open hoop greenhouse. Based on these findings, we propose a disease cycle for P. porri in which oospores germinate in puddles, and zoospores reach the leaves by rain splash and survive in water in the leaf axils, from where they infect the plant by direct penetration or via stomata. When conditions become unfavourable, oospores are produced in the leaves which again reach the soil when leaves decay. Secondary spread of the disease by sporangia does not seem to be important.     

Water-borne spore dispersal in coffee berry disease and its relation to control*

Devices are described which were used to catch rain-dispersed Colletotrichum conidia within and between coffee trees infected with coffee berry disease (CBD). The amount of CBD inoculum dispersed was related to the number of diseased and sporulating berries but not to the sporulating capacity of the fungus in maturing bark. Wet conditions encouraged spore production and dispersal, and spraying with fungicides prolonged sporulation of diseased berries. The amount of pathogenic inoculum, subsequent disease development and crop losses were greatly increased by the presence of only a few diseased berries during growth of the young crop. Spore concentrations were greatest close to diseased berries, but most spores within trees were dispersed downwards through the canopy. Some spores were dispersed between trees by wind-driven rain-splash and vectors such as pickers. Inoculum sources in tree tops are most important during CBD epidemics and disease can be restricted by removing or spraying the tops of multiple-stem trees. Fungicide applied to tree tops effectively controls CBD, because spores dispersed during rain are accompanied by redistributed fungicide     

Effect of wax and lanolin emulsions on the efficiency of potato-blight fungicides in laboratory tests

Four potato-blight fungicides (copper oxychloride, tetrachloroisophthalo-nitrile, zineb and fentin acetate) were formulated either by adding emulsions of paraffin wax or lanolin to solid fungicide dispersed in water, or by dissolving the fungicide in wax or lanolin and then emulsifying the solution; all emulsions were non-creaming and extremely stable. These formulations were compared in the laboratory with commercial wettable powders of the same fungicides for their ability to protect detached potato leaflets against infection by Phytophthora infestans (Mont.) de Bary; in these and in other laboratory tests, the quality of rain-fastness, or tenacity, was involved directly or indirectly. Most of the wax or lanolin formulations gave better protection than the wettable powders. It is suggested that the wax and lanolin acted as viscous stickers, suitably increasing the rain-fastness of deposits on leaflets; and that when the fungicide was dissolved in the wax or lanolin before emulsification, the particle size of the dispersed fungicide was extremely small, a quality that increases biological action.     

THE PATHOLOGY OF HYPODERMELLA LARICIS ON LARCH,LARIX OCCIDENTALS

A study of the larch needle disease caused by Hypodermella laricis provided information on the mode of infection, the manner of spread, and the relationship between the parasite and its host, Larix occidentalis. Infection by spores occurs in early spring as soon as the leaves emerge, but there is no evidence that hyphae invade the dwarf shoots. The fungus disrupts the normal abscission mechanism, and the fructifications and spores of H. laricis develop on the leaves which remain attached to the dwarf shoots. The time of precipitation is a decisive factor in the initiation of the disease, i.e., infection occurs only when precipitation coincides with the emergence of young leaves. However, vulnerability to infection diminishes rapidly as the leaves mature. By observing leaf size and noting the time of rainfall, the severity of infection can be accurately predicted. Several adaptive mechanisms related to successful parasitism in H. laricis are discussed.     

Seasonal changes in primary and secondary inoculum during epidemics of leaf blotch (Rhynchosporium secalis) on winter barley

Seasonal changes in numbers of conidia of Rhynchosporium secalis on debris from previous barley crops infected with leaf blotch (primary inoculum) were monitored in 1985–86 and 1986–87. In 1986–87, changes in numbers of conidia on leaves of plants in the new winter barley crop (secondary inoculum) were also recorded. The greatest increases in production of primary inoculum were in early spring after rain, when temperatures were increasing after periods of sub-zero temperatures when there was little conidial production. Subsequently, more conidia were recovered from this debris after cycles of drying and rewetting than when it remained wet. After January 1987, amounts of secondary inoculum produced on the crop were much greater than amounts of primary inoculum on debris. Most spores were produced on the basal leaves and more spores were present on the September-sown than on the November-sown crop. Thus, while primary inoculum was a source of disease when plants were emerging, secondary inoculum on basal leaves was the main source of disease at stem extension, especially on early-sown crops.     

Green leaf area decline of wheat flag leaves: the influence of fungicides and relationships with mean grain weight and grain yield

A modified Gompertz model was derived to describe the fractional decline in green area of wheat flag leaves in field experiments where green leaf area at time t=100exp[‐exp(‐k(t‐m))]. Curves fitted over time to visual assessments of green leaf area (% of total leaf area) throughout flag leaf life accounted for more than 98% of variation in 45 of 48 wheat cultivar × fungicide treatment (+/?) comparisons. This data set spanned 17 yr and therefore included cultivars of contrasting parentage and age. In the absence of fungicide, green leaf area decline was associated with drought or infection with a number of foliar pathogens including Septoria tritici (sexual stage Mycospherella graminicola), Erysiphe graminis and Puccinia striiformis. Fungicides applied to the flag leaf included propiconazole, propiconazole plus tridemorph, flusilazole or azoxystrobin. Fungicide effects on m (i.e. time to 37% green area) were closely related to fungicide effects (% of untreated) on mean grain weight (variation accounted for (VAF) = 80%) and grain yield (VAF = 85%).     

Studies in vitro and in vivo with powdery mildew fungicides

Droplets of 4-(i-cycloalkylalkyl)-2,6-dinitrophenols often protect areas of leaf very much greater than that of the initial deposit against powdery mildew. For a given alkyldinitrophenol, this type of protection is greater on apple than on marrow leaves. This zonal protection is not correlated with vapour activity in vitro or in vivo, or with inhibition of conidial germination in vitro, but is correlated with the degree of protection obtained when leaves are sprayed to give good cover. By contrast, crotonic esters of these alkyl-dinitrophenols do not show zonal activity, but nevertheless often exhibit protectant activity comparable with that of the parent phenols. These results suggest that exploitation of favourable hydrogen bonding characteristics in the fungicide molecule may lead to better control of fungal diseases in the field as a result of enhanced movement of fungicide in or on the leaf cuticle (zonal movement) or easier penetration of the fungal conidium.     

Dispersal of Pseudocercosporella herpotrichoides Spores from Infected Wheat Straw

Evidence from spore samples collected amongst infected straw spread on fallow ground supported the conclusion that spores of Pseudocercosporella herpotrichoides are dispersed mostly by rainsplash. Most spores travelled a short distance in the larger ballistic splash droplets, although some may have travelled further in smaller airborne droplets. Weekly spore counts from microscope slides under rainshields, a funnel and an impinger, evaluated as samplers for spores of P. herpotrichoides, showed a similar seasonal pattern. The funnel, as the largest sampler, generally collected most spores, but the impinger collected more spores per unit area of sampling surface. Slides sometimes collected spores when none was recovered from other samplers. Young wheat plants, exposed with the samplers and changed weekly, subsequently developed eyespot symptoms for most of the season.     

Dispersal of conidia of Dothidella ulei from Hevea brasiliensis

South American leaf blight caused by Dothidella ulei occurs only in tropical America, on both indigenous and cultivated Hevea spp. The conidium (Fusicladium macrosporum) is a 1-septate, dry, air-borne spore about 40 × 7 μ, occurring on the abaxial surface of dry leaves in dense, powdery, olive-green masses, and with one or both cells collapsed. The conidia adhere to the surface of water droplets, becoming turgid, and are disseminated in splash droplets. A Hirst volumetric trap, placed within a prepared source in north-west Trinidad, showed a diurnal periodicity of conidial production, with a maximum at 10.00 h and minima at night or in the early morning. On rainless days there was also a minor peak at 20.00 h. Transient increases occurred after rain, most of which fell around noon. On wet days almost equal numbers of conidia were dispersed between 10.00 and 12.00 h. Large increases occurred in 87% of all rain showers between 09.00 and 13.00 h. After 13.00 h fewer rain showers caused such increases; the lowest (36%) was between 21.00 and 01.00 h. Twice as many were trapped on sunny days (> 9 h sun) at 09.00 h when there was full sunshine, compared with overcast days (< 5 h sun). A more clearly defined morning maximum occurred on relatively windy days, compared with calmer ones. Conidial sporulation became very low, or ceased, where rain fell below a mean of 3–4 mm per day for at least 20 days. Abundant sporulation occurred with a daily rainfall about twice this amount. The results support the belief that if Dothidella ulei appeared in Malaysia its spread would be rapid and its effects damaging.     

Effects of fungicide timing on control of Rhynchosporium secalis in barley plants

Sprays of captafol, carbendazim, carbendazim + tridemorph + maneb, diclobutrazol, triadimefon or triadimefon + carbendazim all completely protected barley plants in a glasshouse against R. secalis for at least 30 days. However, their effectiveness in preventing disease development when applied after inoculation differed: triadimefon, traidimefon + carbendazim, or diclobutrazol were the most effective, completely preventing symptom development when applied up to 5 days after inoculation to plants grown above 16 °C, and up to 8 days below 8 °C. All the fungicides decreased the number of viable conidia produced by leaf blotch lesions, and when applied to infected plants at G. S. 30, greatly decreased the upward spread of the disease under simulated rain conditions; the most effective fungicides in these respects were triadimefon and triadimefon + carbendazim. The above fungicides and fungicide mixtures, together with the recently introduced materials fenpropimorph and propiconazole were applied to diseased winter barley crops in winter or in spring. All treatments decreased leaf blotch development and increased yields. In most cases, a winter application was more effective than spring applications, particularly if applied in mid-November. The most effective fungicides were triadimefon and propiconazole. The field trials data fitted well with the predictions of performance indicated by the glasshouse investigations.