Development of insecticide resistance and cross-resistance in fenvalerate-, and cypermethrin-selected strains of Earias vittella(fab.)

First-instar Earias vittella (Fab.) larvae were selected with fenvalerate and cypermethrin for 15 successive generations in the laboratory at 28(± 1)°C. The insect developed 7.8-fold resistance to fenvalerate and no resistance to cypermethrin. The fenvalerate-selected strain developed 2800-fold and 1200-fold cross-resistance to endosulfan and carbaryl, respectively. This strain, however, did not manifest cross-resistance to the organophosphorus insecticides, quinalphos, fenitrothion, monocrotophos and malathion, or to the synthetic pyrethroid, cypermethrin. The cypermethrin-selected strain acquired 5-, 4-, and 3-fold cross-resistance to endosulfan, fenvalerate and carbaryl, respectively and no cross-resistance to the above organophosphorus insecticides.     

Concurrent events in the uptake by insects of cypermethrin from a microemulsion formulation

Changes in formulation composition at the site of in-vivo applications of an oil-in-water cypermethrin microemulsion have been determined on American cockroaches (Periplaneta americana). Surface washes of 0.6-μl deposits on femur cuticle recovered decreasing amounts of radio-labelled diluent water, toluene and cypermethrin with time. After 30 min, only cypermethrin (22.5 % w/w initial dose) could be removed in significant amounts. Extraction of cuticle underlying the site of application indicated similar but independent, patterns of initially increasing levels followed by a decline from the maximum, for all three compounds. Recoveries of formulants in the surface washes were utilised to describe the post-application nature of the microemulsion deposit as provided by the formulation phase diagram. The initial and most rapid movement of cypermethrin away from the surface deposit apparently took place via the intact oil-in-water microemulsion. Some 6 min after application, the deposit entered a viscoelastic gel phase with no further phase change indicated.     

Laboratory shelf-life of oil-formulated conidia of the locust and grasshopper fungal pathogen Metarhizium flavoviridae Gams & Rozsypal,in mixtures with the pyrethroid insecticide lambda-cyhalothrin

The addition of 20 ppm lambda-cyhalothrin pyrethroid insecticide to Metarhizium flavoviridae (Fungi: Deuteromycetes) dry conidia in oil kept germination above 80% for 2 and 12 months at temperatures of approximately 30 and 8°C respectively. At 30°C, conidia in oil alone maintained viability for only a few weeks, but this was doubled at 8°C. Even dry conidia retained good viability for only 5 months at the higher temperature. The extended viability of conidia given by adding the pyrethroid to the oil formulation is regarded as very valuable for areas where the fungus is to be used against locusts and grasshoppers.     

Laboratory studies on the effect of temperature and humidity on the life table of the whitefly,Aleurotuberculatus takahashi David & Subramaniam (Hom., Aleyrodidae) from southeastern China

The present paper deals with developmental duration, emergence, longevity and fecundity ofAleurotuberculatus takabashi David & Subramaniam at different temperatures and humidity levels. The developmental time from egg to adult was 81.8, 56.9, 39.6, 29.9, 20.6 days at 15±1, 20±1, 25±1, 30±1, 35±1°C under constant relative humidity (RH) of 70±5%, respectively. At 25±1°C, the total developmental time was slightly affected by humidity, ranging from 46.4 days at 40±5% RH to 39.2 days at 90±5% RH. The developmental threshold and the thermal constant for the stage from egg to adult were 10.1°C and 542.8 day-degrees. It was estimated that the whitefly has about 10 generations a year in Fuzhou region in southeastern China. Lowest mortality rates of 12.4% for the egg, 6.8% for the nymph and 3.1% for the puparium were obtained at 15±1°C, while they were highest with 92.1% for the egg, 48.2% for the nymph and 36.3% for the puparium at 35±1°C. The mortality rates were slightly affected by humidity, ranging from 17.6% at 40±5% RH to 27.9% at 90±5% RH for the egg, 11.2% at 40±5% RH to 19.6% at 90±5% RH for the nymph, and 6.4% at 40±5% RH to 11.6% at 90±5% RH for the puparium. The emergence rate of adults decreased as temperature increased, ranging from 89.1% at 15±1°C to 21.5% at 35±1°C, so did the longevity of adults, ranging from 9.6 days at 15±1°C to 2.9 days at 35±1°C. The number of eggs per female was significantly affected by temperature (P.01), valuing 29.4 eggs per female at 15±1°C, 36.7 at 20±1°C, 52.4 at 25±1°C, 42.9 at 30±1°C, and 6.1 at 35±1°C. The optimal temperature for reproduction was about 25°C.     

Comparative biology and life table of Habrobracon hebetor (Hymenoptera: Braconidae) on Anagasta kuehniella (Lepidoptera: Pyralidae) at five constant temperatures

Habrobracon hebetor Say is an ectoparasitoid that has been used as a control agent of various lepidopteran pests. Temperature-dependent life table and thermal characteristics of H. hebetor are important in understanding the dynamics of host–parasitoid relationships and for optimizing biocontrol programmes. The influence of five constant temperatures (15, 20, 25, 30 and 35 °C) on the biology of H. hebetor when parasitizing Anagasta kuehniella Zeller was studied. The survival rate of immature stages increased from 16.67% to 83.81% as temperature increased from 15 to 30 °C and then decreased at 35 °C. Total development time ranged from 45.70 days at 15 °C to 7.10 days at 35 °C. The lower temperature threshold for immature stages varied slightly around a value of 11–12 °C. The net reproductive rate (R₀) values were significantly different among temperatures and the highest value was found at 30 °C (85.10). The high survival rate and net reproductive rate combined with a relatively short generation time at 30 °C resulted in the intrinsic rate of increase (r_m) being highest (0.312 d^?1) at this temperature. Considering the acquired results, the temperature range between 25 and 30 °C was optimal for H. hebetor.     

The dormancy of wild oat seed (Avena fatua L.) from plants grown under various temperature and soil moisture conditions

Wild oat plants of types fA, fB and fC were grown at a constant 15 or 20°C during the period of seed maturation. Seed of the three types differed little in dormancy when grown at 15°C, but at 20°C a larger proportion of seeds of type fA were dormant compared with fB or fC. Overall, dormancy of seed produced at 15 and 20°C was 97 and 63% respectively. Plants of another collection of type fB were grown from seed at 15 or 20°C with or without water stress applied only from the time of panicle emergence. Water stress and high temperature reduced viable seed production. Seed dormancy was tested immediately after collection by planting the seed in soil, and by Petri dish tests. Further Petri dish tests were made after 6 months storage. Seedling emergence in the first autumn from seeds of plants matured without water stress at 15°C was 10% compared with 30% for seeds grown at 20°C. Seeds grown with water stress at 15°C gave 47%, and at 20°C 78% emergence. The majority of emergence from seeds formed at 15°C without water stress occurred in the second spring after burial. Petri dish tests support these findings and suggest that seeds produced in hot dry summers are less dormant than those produced in cool moist ones.     

Effect of burning and high temperature on survival of Xanthomonas translucens pv. pistaciae in infected pistachio branches and twigs

This paper reports the efficacy of burning and heat‐treating pistachio branches and twigs as a means of disposing of prunings from trees infected with Xanthomonas translucens pv. pistaciae (Xtp). Burning of pistachio wood, naturally infected with Xtp, was conducted twice under field conditions. Viable Xtp was detected in some non‐burned wood, but not in charcoal, ash or partially burned wood. Controlled laboratory experiments were conducted with pure cultures of Xtp and naturally and artificially infected pistachio wood. In liquid culture, 65°C was lethal to Xtp, whereas survival at 60°C or less varied with culture medium and duration of exposure. Xtp survived in infected wood exposed to 40–55°C for at least 60 min but was killed by exposure to 60°C for 15 min or more. Overall, the results of burning and heat treatment were consistent, and confirmed that burning was a reliable eradication technique to dispose of infected wood, such as prunings, providing the pathogen was exposed to a temperature of 60°C or greater for at least 15 min.     

Partial Purification of Thai Isolate of Citrus Huanglongbing (Greening) Bacterium and Antiserum Production for Serological Diagnosis

We aimed to improve the purification of citrus Huanglongbing (greening) bacterium (HB), Candidatus Liberobacter asiaticum and to produce an antiserum against HB. Periwinkle plants Catharantus roseum L. graft-inoculated with HB were used to produce an antiserum. All young leaves of new shoots incubated at 20–25°C and 25–30°C, a few mature leaves incubated at 20–25°C, and all mature leaves incubated first at 25–30°C and later transferred to 20–25°C developed yellowing symptoms and were then used to prepare immunogen. The HB was partially purified from these leaves by an improved method that included a macerating enzyme treatment of the midribs of infected leaves and homogenization of infected phloem sieve tissues. An antiserum raised against partially purified HB reacted clearly at a dilution of 1/16 with HB-infected citrus extract prepared at a concentration of 40 times, but did not react with healthy or tristeza virus-infected citrus extract in microprecipitin tests. Received 23 August 2002/ Accepted in revised form 4 December 2002     

Effect of temperature during burial on dormant and non-dormant seeds of Lamium amplexicaule L. and ecological implications

Spring-produced seeds of Lamium amplexicaule L. were dormant at maturity in May and after-ripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6 and 20/10°C) and non-dormant at high (25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5 and 15/6°C, and non-dormant seeds germinated to high percentages at 5, 15/6, 20/10, 25/15 and 30/15°C. Seeds that became conditionally dormant at 5°C afterripened completely (i.e. became non-dormant) after transfer to 30/15°C. Buried seeds that became non-dormant in a non-temperature-controlled glasshouse during summer were still non-dormant after 12 weeks of storage at 30/15°C, while those stored at 5°C for 12 weeks had entered conditional dormancy. Thus, low temperatures cause reversal of the afterripening that takes place at high temperatures, but not that which takes place both at low and at high temperatures. Low winter temperatures cause dormant autumn-produced seeds and non-dormant seeds in the soil seed pool to become conditionally dormant. The ecological consequences of these responses to temperature are discussed in relation to the timing of seed germination in nature.     

Functional responses of the parasitoid,Ertmocerus longipes Compere (Hym., Aphelinidae) to densities of the whitefly,Aleurotuberculatus takahashi David et Subramaniam (Hom., Aleyrodidae) at different temperatures

The present study dealt with the functional responses of the parasitoid,Eretmocerus longipes Compere (Hym., Aphelinidae) to the densities of the whitefly,Aleurotuberculatus takahashi David et Subramaniam (Hom., Aleurodidae) at different temperatures under the laboratory conditions. The results showed that when the initial densities ofA. takahashi-3rd instar were raised from 10 to 320 ind./leaf, the numbers of parasitized nymphs increased as well, ranging from 7.0 to 23.1 at 20°C, 9.8 to 42.9 at 25°C, 6.7 to 39.9 at 30°C, and 1.8 to 8.3 ind./leaf at 35°C, respectively. The Holling Disk Equation was introduced to build up the models of functional responses. The response curves remained type II, although the numbers of parasitized nymphs were significantly different under different temperatures. The suitable initial densities of the host whitefly for parasitization were about 80 individuals per leaf. A negative relation was observed between the initial densities of the whitefly and the parasitization rates by the parasitoid. An increase in the initial densities ofA. takahashi-3rd instars ranging from 10 to 320 ind./leaf resulted in a decrease in the parasitization rate byE. longipes ranging from 70.0% to 7.2% at 20°C, 98.0% to 13.4% at 25°C, 67.0% to 12.5% at 30°C and 18.0% to 2.6% at 35°C with a value of 0.2877 was significantly smaller than that at 20°C with a vlaue of 1.3354, that at 25°C with a value of 1.6465 and that at 30°C with a value of 1.1199, respectively (p<0.01). The handling time (Th) forE. longipes was 0.1521 at 35°C, significantly longer than 0.0510 at 20°C, 0.0289 at 25°C and 0.0320 at 30°C, respectively (p<0.01). The maximum loading number (K) of the parasitized nymphs with a value of 34.5 ind./leaf at 25°C was similar to that with a value of 31.2 ind./leaf at 30°C, about 1.8 times as high as that with a value of 19.6 ind./leaf at 20°C and 4 times more than that with a value of 6.6 ind./leaf at 35°C. It was suggested that temperature affected the functional response by balancing searching rate and handling time. The optimal temperature range for the functional responses ofE. longipes to the densities ofA. takahashi-3rd instar was 25° to 30°C.     

Distribution and seed production of Cirsium arvense (L.) Scop, in Victoria, Australia

In 1971 the net area of Cirsium arvense in Victoria was 1300 ha in permanent pasture, 120 ha in cropping land and 40 ha in non-agricultural land. In ten farms in the most heavily infested parish (approximately 100 km²). C. arvense was present in 35 % of the fields and occurred in some highly productive legume-based pastures. The most common control practice on these farms was pasture slashing. It was considered that the weed had been on the farms for 40–80 years. At a constant temperature of 20°C, but not at alternating temperatures, the germination percentage of seed was enhanced by pre-chilling. At constant temperatures the germination percentage was higher at 30°C than at lower temperatures. Alternating temperatures that included 30°C also increased the germination percentage, but it was depressed at 15°/40°C. The germination percentage of seed from forty sites was 52%-97% and some seed was formed where male and female plants were separated by distances of up to 390 m. However, no seed was found in about a third of the parishes examined. Distribution et production de semences de Cirsium arvense (L.) Scop, dans I'etat de Victoria en Australie. En 1971, la surface nette occupée par Cirsium arvense dans pétat de Victoria était de 1300 ha dans les prairies permanentes, de 120 ha dans les terres cultivées et de 40 ha dans les terres non agricoles. Dans 10 fermes situées dans la partie la plus infestée (approximativement 100 km²) C. arvense était present dans 35% des champs et apparaissait dans quelques pâtures hautement productives â base de 1égumineuses. La méthode de lutte la plus fréquente dans ces fermes était la pâture intensive. 11 était admis que la mauvaise herbe était présente dans les exploitations depuis 40 à 80 ans. A la temperature constante de 20°C, maisnon à des tempértures alternées, le pourcentage de germination des semen-ces fut augmenté par une réfrigération préalable. A température constante, le pourcentage de germination fut plus élevé k 30°C quà des temperatures plus basses. Les températures alternées, qui comprenaient celle de 30°C augmentérent aussi le pourcentage de germination, mats celui-ci diminua à 15°/40°C. Les pourcentages de germination de semences de 40 provenances différences se situa entre 52% et 97%; quelques semences furent formées dans des cas où les plantes mäles et les plantes femelles étaient séparées par des distances atteign-ant 390 m. Toutefois aucune semence ne fut trouvée dans un tiers environ des localities examinées. Verbreitung und Samenproduktion von Cirsium arvense (L.) Scop, in Victoria, Australien Die mit Cirsium arvense verseuchte Flfiche in Victoria im Jahre 1971, gliedert sich auf in: 1 300 ha Daucrweide. 120 ha Ackerland und 40 ha nicht-landwirtschafllich genutzte Fläche. In 10 Betrieben des am stftrksten verseuchten Bezirks (ca. 100 km²), war C. arvense in 35% der Felder vorhanden und kam in einigen hochproduktiven Leguminosenweiden vor. Die gebräuchlichste Bekämpfungsmassnahme in diesen Betrieben war das Abmiihen mit Schlegelhilckslem. Es wird angenommen, dass dieses Unkraut seit 40 bis 80 Jahren in den Betrieben vorhanden ist. Bei einer konstanten Temperatur von 20°C, nicht aber bei Wecheseltemperaturen, wurde durch vorheriges Einfrieren die Keimungsrate erhöht. Bei konstanten Temperaturen war sie bei 30°C hSoUher als bei niedrigeren Temperaturen. Wechseltemperaturen die 30°C einschlossen, erhöhten auch die Keimungsrate; bei 15°C/40°C war sie aher geringer. Die Keimung der Samen von 40 Siandorten betrug 52% bis 97%. Wenn weibliche und mflnnliche Pfianzen his zu 390 m von einander entfernt waren. wurden noch einige Samen gebildet. In etwa einem Drittel der untersuchten Bezirke wurden jedoch keine Samen gefunden.     

Effect of temperature on primary infection by Plasmodiophora brassicae and initiation of clubroot symptoms

A study was conducted to assess the effect of temperature on infection and development of Plasmodiophora brassicae in root hairs of Shanghai pak choi (Brassica rapa subsp. chinensis) and on initiation of clubroot symptoms. Ten‐day‐old seedlings were grown in liquid‐sand culture, inoculated with resting spores and maintained in growth cabinets at 10, 15, 20, 25 and 30°C. Seedlings were harvested at 2‐day intervals, starting 2 days after inoculation (DAI) and continuing until swelling of the tap root was observed (maximum 28 days). Roots were assessed for root hair infection (RHI), stage of development of infection (primary plasmodia, zoosporangia, release of zoospores, secondary plasmodia), symptom development, and for clubroot severity at 24 DAI. Temperature affected every stage of clubroot development; RHI was highest and visual symptoms initiated earliest at 25°C, intermediate at 20 and 30°C, and lowest and latest at 15 and 10°C. Root hair infection was observed at every temperature, but clubroot symptoms developed only above 15°C. A substantial delay in the development of the pathogen was observed at 10 and 15°C. No symptoms were observed at 28 DAI in plants grown at 10°C. Swelling of the tap root was visible at 28 DAI in plants at 15°C, 14 DAI at 20 and 30°C, and 10 DAI at 25°C. These results support and explain the observation in companion studies that cool temperatures result in slower development of clubroot symptoms in brassica crops.     

Potential for eradication of the exotic plant pathogens Phytophthora kernoviae and Phytophthora ramorum during composting

Temperature and exposure time effects on Phytophthora kernoviae and Phytophthora ramorum viability were examined in flasks of compost and in a large‐scale composting system containing plant waste. Cellophane, rhododendron leaf and peat‐based inoculum of P. kernoviae and P. ramorum isolates were used in flasks; naturally infected leaves were inserted into a large‐scale system. Exposures of 5 and 10 days respectively at a mean temperature of 35°C in flask and large‐scale composts reduced P. kernoviae and P. ramorum inocula to below detection limits using semi‐selective culturing. Although P. ramorum was undetectable after a 1‐day exposure of inoculum to compost at 40°C in flasks, it survived on leaves exposed to a mean temperature of 40·9°C for 5 days in a large‐scale composting system. No survival of P. ramorum was detected after exposure of infected leaves for 5 days to a mean temperature of ≥41·9°C (32·8°C for P. kernoviae) or for 10 days at ≥31·8°C (25·9°C for Phytophthora pseudosyringae on infected bilberry stems) in large‐scale systems. Fitted survival probabilities of P. ramorum on infected leaves exposed in a large‐scale system for 5 days at 45°C or for 10 days at 35°C were <3%, for an average initial infection level of leaves of 59·2%. RNA quantification to measure viability was shown to be unreliable in environments that favour RNA preservation: high levels of ITS1 RNA were recovered from P. kernoviae‐ and P. ramorum‐infected leaves exposed to composting plant wastes at >53°C, when all culture results were negative.     

Functional degeneration of the resistance gene nsv against Melon necrotic spot virus at low temperature

The single recessive gene, nsv, which confers resistance against Melon necrotic spot virus (MNSV), has recently been used to develop virus-resistant melon cultivars in Japan. However, the Chiba isolate of MNSV, a common isolate in Japan, infected resistant cultivars when inoculated melon plants were grown at 15°C. Viral RNAs accumulated in protoplasts from resistant cultivars at both 15 and 20°C. Mechanical inoculation of the cotyledons caused MNSV to spread throughout the leaves at 15°C, but not at 20°C. These results support our novel hypothesis that a temperature-sensitive inactivation of disease resistance genes occurs at the nsv locus in melon cultivars with the resistance gene grown at temperatures below 20°C. The first and second authors contributed equally to this research.     

Pathogenicity of <Emphasis Type="Italic">Mycochaetophora gentianae</Emphasis>, causal fungus of gentian brown leaf spot,as affected by host species,inoculum density,temperature, leaf wetness duration,and leaf position

When the influence of host species, inoculum density, temperature, leaf wetness duration, and leaf position on the incidence of gentian brown leaf spot caused by Mycochaetophora gentianae, was examined, the fungus severely infected all seven Gentiana triflora cultivars, but failed to infect two cultivars of G. scabra and an interspecific hybrid cultivar. Inoculum density correlated closely with disease incidence, and a minimum of 10² conidia/mL was enough to cause infection. In an analysis of variance, temperature and leaf wetness duration had a significant effect upon disease incidence, which increased with higher temperature (15–25°C) and longer duration of leaf wetness (36–72 h). No disease developed at temperatures lower than 10°C or when leaf wetness lasted <24 h. At 48-h leaf wetness, disease incidence was 0, 28, 77, and 85% at 10, 15, 20, and 25°C, respectively. Middle and lower leaves on the plant were more susceptible than upper leaves. In microscopic observations of inoculated leaves, >50% of conidia germinated at temperatures >15°C after 24-h leaf wetness. More appressoria formed at higher temperatures (15–25°C) with extended duration of leaf wetness (24–72 h). At 48-h leaf wetness, appressorium formation was 0, 8, 26, and 73% at 10, 15, 20, and 25°C, respectively. These results suggest that temperature and leaf wetness duration were important factors for infection of gentian leaves.     

Seasonal changes in the germination responses of buried Lamium amplexicaule seeds

Spring-produced seeds of Lamium amplexicaule L. were buried in pots of soil in an unheated glasshouse in June 1978, and at 1–2-month intervals, for 27 months, they were exhumed and tested for germination in light and darkness at temperatures simulating those in the habitat from early spring to late autumn. Freshly-matured seeds were dormant, but by autumn 85% or more germinated in light at 15/6, 20/10, 25/15 and 30/15°C but only 7% or less in darkness. During late autumn and winter germination in light decreased at 25/15 and 30/15 °C but not at 15/6 and 20/10 °C, and germination in darkness increased at 15/6 and 20/10 °C. During late winter and early spring germination in light at 15/6 and 20/10 °C decreased, and seeds lost the ability to germinate in darkness. By the second autumn of burial, seeds germinated to near 100% in light at 15/6 to 30/15 °C and to 10–25% in darkness at 15/6 and 20/10 °C. The cycle of germination responses was repeated during the second winter and spring and the third summer of burial. Autumn-produced seeds were dormant when buried in November 1979, but by spring they germinated to 81 and 36% at 15/6 and 20/10 °C, respectively, in light. These seeds afterripened further during summer. The consequence of seasonal changes in germination responses is that (1) seeds can germinate in the habitat in late summer, autumn and spring but not in early- to mid-summer or in late autumn and winter and (2) during both germination seasons, seeds produced during the previous spring(s) and/or autumn(s) can germinate.     

Überleben von Ralstonia solanacearum Biovar 2 (Rasse 3), dem Erreger der Schleimkrankheit der Kartoffel, in Boden und auf verschiedenen Materialien (Mikrokosmos)

Microcosm studies were carried out to test the survival of Ralstonia solanacearum biovar 2 (race 3) in soil at the permanent wilting point (wp) water content and at field capacity (fc) water content and on various material. Soils were placed at permanent ?5°C, 4°C, 15°C and 20°C and weekly fluctuating ?10/0/+10°C and the material at 5, 15 °C, 20°C with relative humidity (rh) uncontrolled or at constant 10% or 90%. In soil, survival was clearly dependent on temperature independent of water content. At 20°C Ralstonia solanacearum could be reisolated up to 364 days, at 15°C up to 290 days, at 4°C up to 209 days and at fluctuating temperatures (?10/0/+10°C) only up to 18 days. The lower the temperature, the more the population declined. At 15°C and 20°C appr. 10⁷ cfu/g soil were detected after 100 days, whereas at ?5°C only 10² cfu/g soil were detected after only 18 days. The pathogen was longer detectable in sandy-clay loam than in lighter sandy soil. It could be longer reisolated at wilting point and the populations did not decline as rapidly as at field capacity. Ralstonia solanacearum could best survive on material surfaces like rubber, plastic and varnished metal with maximum survival of 40 days at 5°C and 10% rh. In general there is a low risk of Ralstonia solanacearum overwintering under European climatic conditions when the fields are cleared of plant debris and the soil is frozen. Contamined material surfaces pose the risk of pathogen transmission to healthy tubers.     

Survival of Fusarium circinatum in soil and Pinus radiata needle and branch segments

Survival of Fusarium circinatum in colonized pine needles and wood pieces was measured. Naturally colonized branches and their needles were cut into small pieces and placed in mesh bags on the soil surface at two locations in northern Spain. Pieces were recovered periodically, cultured on a selective medium, and microscopically examined to identify the species. After 507 days, F. circinatum was recovered from 0 to 27% of the wood pieces and from none of the needles. After 858 days, F. circinatum was not recovered from any wood pieces but was found to be present on 1 out of 220 needle pieces analysed. Artificially infested pieces of wood and needles were placed on 5‐mm sieved soil either in plastic boxes at controlled temperature or in mesh bags under field conditions. No survival was recorded after 794 days under field conditions and the decline over time occurred more rapidly in inoculated pieces under field conditions. Soil was also infested with conidia of F. circinatum and survival was estimated. No conidia were recovered after 224 days at 30 °C, although at 20 and 5 °C the respective populations were 20 and 3700 cfu/g soil. Fusarium circinatum was not recovered from 2‐mm‐sieved soil collected under pitch canker‐infected pines. Results indicate that branch segments and needles naturally colonized by F. circinatum will not be a potential source of inoculum, and the fungus in soil is not likely to contribute to reinfection of new plantations after 2 years.     

Overwintering of brown leaf spot fungus, Mycochaetophora gentianae, in infected gentian leaves as the primary inoculum source

Overwintering of the brown leaf spot fungus, Mycochaetophora gentianae, in infected gentian leaves was studied in Iwate, northern Japan. Sporophores were produced on overwintered, infected leaves when they were sampled from January to July, but not in August after incubation in high humidity at 15 °C. Symptoms developed on gentian plants grown in soil artificially infested with overwintered, infected leaves that were either left throughout the experiments or removed before planting. Few lesions developed when plants were grown in soil infested with conidia. These results indicate that M. gentianae can overwinter in infected leaves, which act as the primary inoculum source.     

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.