UV protectants for Candida oleophila (strain O), a biocontrol agent of postharvest fruit diseases

This study investigated the influence of UV‐B radiation (280–320 nm) on survival of Candida oleophila strain O, an antagonist yeast that prevents postharvest diseases caused by Botrytis cinerea and Penicillium expansum on apple and pear fruits. Lethal doses (LD₅₀ and LD₉₀) were, respectively, 0·89 and 1·45 Kj m^?2 for in vitro exposure and 3·06 and 5·5 Kj m^?2 for in vivo exposure. A screening test of UV‐B protectants for strain O was also evaluated under in vitro and in vivo conditions. The in vitro results showed that sodium ascorbate (0·1% and 0·01%), riboflavin (0·1%) and uric acid (0·1% and 0·01%) were the most effective and most suitable protectants. However, only riboflavin (0·1%) and uric acid (0·1%) were effective under in vivo conditions. The efficacy obtained with strain O against P. expansum, when subjected to UV‐B radiation, was 75·0% and 49·2% for pathogen concentrations of 10⁵ and 10⁶ spores mL^?1, respectively. Adding riboflavin to strain O gave a similar efficacy (64·2%). Applying strain O together with uric acid (0·1%) was less active (47·7%). Nonetheless, its efficacy when applied with the antioxidants sodium ascorbate (71·1%) or ascorbic acid (82·5%) was the greatest. Riboflavin and uric acid were the most cost‐effective protectants, and could be included in the final formulation of strain O when applied preharvest.     

Evaluation of different methods for the characterization of carrot resistance to the alternaria leaf blight pathogen (Alternaria dauci) revealed two qualitatively different resistances

Alternaria leaf blight (ALB), caused by Alternaria dauci, is one of the most damaging foliar diseases of carrot worldwide. The aim of this study was to compare different methods for evaluating levels of carrot resistance to ALB. Three techniques were investigated by comparison with a visual disease assessment control: in vivo conidial germination, a bioassay based on a drop‐inoculation method, and in planta quantification of fungal biomass by quantitative PCR (Q‐PCR). Three carrot cultivars showing different degrees of resistance to A. dauci were used, i.e. a susceptible cultivar (Presto) and two partially resistant genotypes (Texto and Bolero), challenged with an aggressive or a very aggressive isolate of A. dauci. Both partially resistant genotypes produced a higher mean number of germ tubes per conidium (up to 3·42±0·35) than the susceptible one (1·26±0·18). The drop‐inoculation results allowed one of the partially resistant genotypes (Bolero, log₁₀(S+1) = 1·34±0·13) to be distinguished from the susceptible one (1·90±0·13). By contrast, fungal growth measured by Q‐PCR clearly differentiated the two partially resistant genotypes with log₁₀(I) values of 2·77±0·13 compared to the susceptible cultivar (3·65±0·13) at 15 days post‐inoculation. This result was strongly correlated (r² = 0·91) with the disease severity index scored at the same date. Data obtained with the different assessment methods strongly suggest that the Texto and Bolero genotypes have different genetic resistance sources.     

Factors affecting glyphosate activity in Imperata cylindrica (L.) Beauv. and Cyperus rotundus L. II: effect of shade

Imperata cylindrica and Cyperus rotundus were grown under three different light regimes; unshaded, 50% shade, and 75% shade and no shade plus 75% shade before and after spraying, (temporary shade) in a heated greenhouse. Six weeks after the start of the experimenis, glyphosate was applied to the plants at 0·2, 0·4 and 0·8 kg/ha (for Imperata) or 0·3, 0·6 and 1·2 kg/ha (for Cyperus). Glyphosate toxicity was enhanced as shade increased. In Imperata, all shade regimes at all rates of glyphosate eaused greater damage to the plants than the unshaded regime. The reduction in shoot dry weight, rhizome dry weight and total carbohydrate content of Imperate rhizotties at 75% continuous and temporary shaiie conditions, with the lowest rate of glyphosate, was almost twice as much as the reduction in the same features m the unshaded plants caused by the highest rate of glyphosate. In Cyperus. glyphosate at the intermediate and highest rates decreased the shoot dry weight at 75% continuous shade by 79% and 98% respectively. Plants in 50% shade were significantly affected only at the highest rate of glyphosate. Sprouting ability of the tubers al 75% continuous shade was inhibited when the tubers were replanted for recovery. Enhanced toxicity of glyphosate in reduced light intensity was attributed to the morphological changes in the nature of the leaves caused by shade.     

Effectiveness of Carvacrol Derived from Thujopsis dolabrata var. hondai Sawdust against Thecodiplosis japonensis (Diptera: Cecidomyiidae)

The larvicidal component from sawdust of Thujopsis dolabrata var. hondai (Family Cupressaceae) against the pine needle gall midge (Thecodiplosis japonensis) was isolated by chromatographic techniques and characterized by spectral analysis as carvacrol. In a laboratory study using the impregnated filter paper method, carvacrol was more toxic to T. japonensis larvae than β-thujaplicine, cedrol, α-terpinol, thujone or thymol. In field studies with soil injections of carvacrol, this compound exhibited potent larvicidal activity, suggesting that this activity might be attributable to fumigant action. In a test with trunk implantation, a mixture of carvacrol and phosphamidon (0·15+0·15 ml cm^-1 diameter at breast height) revealed much more potent larvicidal activity than phosphamidon alone (0·3 ml cm^-1 DBH) in spite of little or no larvicidal activity of carvacrol alone (0·3 ml cm^-1 DBH), indicating a possible synergistic effect. As a naturally occurring insecticide, carvacrol could be useful as a new preventive agent against damage caused by T. japonensis. © 1997 SCI.     

Increased resistance to fusarium wilt in transgenic tobacco lines co‐expressing chitinase and wasabi defensin genes

Marker‐free transgenic tobacco (Nicotiana tabacum) lines containing a chitinase (ChiC) gene isolated from Streptomyces griseus strain HUT 6037 were produced by Agrobacterium‐mediated transformation. One marker‐free transgenic line, TC‐1, was retransformed with the wasabi defensin (WD) gene, isolated from Wasabia japonica. Of the retransformed shoots, 37% co‐expressed the ChiC/WD genes, as confirmed by western and northern analyses. Southern blot analysis showed that no chromosomal rearrangement was introduced between the first and the second transformation. Transgenic lines either expressing ChiC or WD, or co‐expressing both genes were challenged with Fusarium oxysporum f.sp. nicotianae (Fon). Assessment of in vitro plant survival in the presence of Fon showed that transgenic lines co‐expressing both genes had significantly enhanced protection against the fungus (infection indices 0·0–1.·2) compared with corresponding isogenic lines expressing either of the genes (infection indices 2·5–9·8). Whole‐plant infection indices in transgenic lines were significantly related (r = 0·93, P < 0·01) to the extent of root colonization of the host, which ranged from 2·1% to 11·3% in lines co‐expressing both genes, and from 16·8% to 37·7% in lines expressing just one of the genes (compared with 86·4% in non‐transformed controls). Leaf extracts of transgenic lines also inhibited mycelial growth of Fon in vitro and caused hyphal abnormalities.     

Effect of the ecdysone agonists,RH-2485 and tebufenozide,on the southwestern corn borer,Diatraea grandiosella

The effect of the ecdysone agonists RH-2485 (proposed name methoxyfenozide) and tebufenozide (RH-5992), was examined on eggs and larvae of the southwestern corn borer, Diatraea grandiosella Dyar. Both compounds exhibited a concentration-dependent ovicidal activity. More than 95% of eggs died when egg masses were dipped in solutions of 100 or 200 mg liter^-1 of either compound in acetone+distilled water (1+1 by volume). Although some eggs treated with 1 or 10 mg liter^-1 of the compounds hatched, the survival rate was low. Newly hatched larvae were fed for seven days on an artificial diet containing RH-2485 or tebufenozide. The LC₅₀ values were 0·049 mg kg^-1 for RH-2485 and 0·185 mg kg^-1 for tebufenozide, showing that RH-2485 was about four times more active than was tebufenozide. Although increasing the time of exposure to either compound decreased the LC₅₀ value significantly, the relative potency of RH-2485 versus tebufenozide was not changed. Newly ecdysed 4th-instar larvae fed with diets containing 0·125, 0·25 or 0·5 mg kg^-1 RH-2485 or tebufenozide ceased feeding approximately 8 h after exposure, indicating that larvae had prematurely entered a molting cycle. Larvae treated with RH-2485 ecdysed earlier and died more quickly than those treated with tebufenozide. Ingestion of sublethal concentrations of RH-2485 (0·005 and 0·01 mg kg^-1) or tebufenozide (0·03 and 0·06 mg kg^-1) retarded larval growth, and decreased pupal weight and adult emergence. Increasing exposure time to tebufenozide tended to increase the larval mortality, significantly retarded larval growth, and decreased the mean weights of male and female pupae and adult emergence. RH-2485 (0·125 and 0·25 mg kg^-1) and tebufenozide (0·25 and 0·5 mg kg^-1) were lethal to newly hatched larvae, even after diets containing these compounds were held for 20 days at 30°C under long days (16 h light: 8 h dark). Our results suggest that field trials to assess the potential of RH-2485 and tebufenozide to control D. grandiosella are warranted. © 1998 SCI     

Control of Achillea millefolium L. (yarrow) by rotary cultivation and glyphosate

Various control strategies for Achillea millefolium L. (yarrow) were investigated in a dense stand of the weed at Lincoln College in 1977–1978. In early spring plots were either rotary cultivated or left undisturbed. In late spring, plots of both previous treatments were either left undisturbed, rotary cultivated or sprayed with glyphosate at 1·5 kg ha^?1. The whole experiment was rotary cultivated twice 1 week later and sown with Hordeum vulgure L. cv. Zephyr (barley) at 144 kg seed ha^?1. MCPA + dicamba at 0·9+0·15 kg ha^?1 was applied to half of each plot when the second node was detectable (Zadok 32). Rotary cultivation and glyphosate both substantially reduced the regrowth of A. millefolium but glyphosate reduced regrowth by a greater proportion when applied to undisturbed plants than when applied to plants regenerating after cultivation. Both gave a more than 95% reduction compared to the control (rotary cultivation only at sowing time) in the amount of A. millefolium present in the barley stubble in the autumn. MCPA + dicamba caused seedling mortality but did not affect the numbers of primary shoots from rhizome fragments. The grain yield of the barley increased from 2·91 t ha^?1 when A. millefolium was not controlled to 4·23 t ha^?1 with good control. The barley yield appeared to be restricted by competition from regenerating A. millefolium and by a nitrogen deficiency induced in some regimes by nitrogen immobilization in decaying rhizomes.     

Nematicidal activity of the leaf powder and extracts of Myrtus communis against the root‐knot nematode Meloidogyne javanica

Nematicidal activity of the leaf powder, leaf extracts and formulated leaf extracts of Myrtus communis, an evergreen shrub that is widely distributed in Israel and other Mediterranean countries, was evaluated using the root‐knot nematode Meloidogyne javanica in in vitro and pot experiments. Leaf powder added to sand at 0·1% (w/w) reduced the number of juveniles recovered from the sand by more than 50%. Reduction in galling index and number of nematode eggs on tomato roots was also observed by incorporating the leaf powder at 0·1–0·4% (w/w) in the soil in pot experiments. Leaf powder extracts with methanol or ethanol showed the highest nematicidal activity among all extracts tested. Emulsifiable concentrates of leaf‐paste extract at a concentration as low as 0·005% (a.i., w/w) reduced the number of juveniles recovered from treated sand and the gall index of cucumber seedlings. The extract paste at 26 g m^?2 was also effective in reducing the gall index of tomato plants in field‐plot experiments. The leaf powder at 0·2% and the formulated leaf‐paste extract at 0·02% were also nematicidal to Tylenchulus semipenetrans and Ditylenchus dipsaci, but not to Pratylenchus penetrans or Steinernema feltiae. At least three nematicidal compounds were found in the leaf extract upon fractionation by thin‐layer chromatography. The results suggest that the leaf powder and paste extract of M. communis are potential nematicides against root‐knot nematodes.     

Evaluation du stock en semences de la morelle jaune (Solanum elaeagnifolium Cav.) dans le sol du Tadla (Maroc)

Assessment of the stock of Solaneum elaeagnifolium Cav. seeds in the soil of the Tadla (Morocco) On the basis of soil samples from four fields on the irrigated perimeter of the Tadla (Central Morocco), selected from the area most heavily infested with Solanum elaeagnifolium, estimates of the stock of seeds of this perennial weed revealed a mean value of 375 seeds m^?2 to a depth of 60 cm (dead + viable seeds). The average for the viable seed stock, however, is 163 seeds m^?2 to a depth of 60 cm, or an average of 43·5% of the total stock of seeds counted. The average distribution profile of the seeds of S. elaeagnifolium in the soil is as follows: 71·7, 25·1 and 3·2%, respectively, in the 0–20, 20–40 and 40–60 cm horizons. The vertical distribution of viable seeds followed the same profile as the overall stock; thus we found 73 and 27% of viable seeds were located in the 0–20 and 20–40 cm horizons, respectively.     

Infection routes for Sclerotinia sclerotiorum in apetalous and fully petalled winter oilseed rape

Near‐isogenic lines (NILs) of apetalous (AP) and fully petalled (FP) winter oilseed rape were used to investigate infection by Sclerotinia sclerotiorum, which occurs mainly via infected petals adhering to leaves in FP oilseed rape. AP1 flowers had an average of 1·4 and 0·8 petals per flower in field and polytunnel experiments, respectively. In field experiments there were no significant differences between counts of FP1 petals, FP1 stamens and AP1 stamens adhered to leaves during flowering. At any one sample time, significantly more stamens tested positive for S. sclerotiorum on AP1 than FP1 NILs, e.g. in 2004, at early flowering 37·5% and 24·2% of stamens tested positive on AP1 and FP1 NILs, respectively. In polytunnel experiments, there were significantly more sclerotinia lesions per plant in the FP1 than in the AP1 NIL. The AP1 NIL did not avoid infection completely, probably because it produced some petals, and lesions were initiated from adhered stamens as well as petals. However, while 8·5% and 16·3% of petals initiated lesions in FP1 and AP1 NILs, respectively, only 2·5% and 1·0% of stamens initiated lesions in FP1 and AP1 NILs, which suggests stamens may be less infective than petals. In field experiments the AP1 NIL had significantly less incidence of sclerotinia stem rot than the FP1 NIL in 2004 (4·9% and 7·0%, respectively). However, there was no significant difference in stem rot incidence between AP and FP lines in 2005 (3·6% and 4·3%, respectively) or 2006 (5·5% and 3·9%, respectively).     

Relationship between disease severity and escape of Pseudoperonospora cubensis sporangia from a cucumber canopy during downy mildew epidemics

Fundamental to the development of models to predict the spread of cucurbit downy mildew is the ability to determine the escape of Pseudoperonospora cubensis sporangia from infected fields. Aerial concentrations of sporangia, C (sporangia m^?3), were monitored using Rotorod samplers deployed at 0·5 to 3·0 m above a naturally infected cucumber canopy in two sites in central and eastern North Carolina in 2011, where disease severity ranged from 1 to 40%. Standing crop of sporangia was assessed each morning at 07·00 h EDT and ranged from 320 to 16 170 sporangia m^?2. Disease severity and height above the canopy significantly (P < 0·0001) affected C with mean concentration (C_m) being high at moderate disease. Values of C_m decreased rapidly with canopy height and at a height of 2·0 m, C_m was only 7% of values measured at 0·5 m when disease was moderate. Daily total flux (F_D) was dependent on disease severity and ranged from 5·9 to 2242·3 sporangia m^?2. The fraction of available sporangia that escaped the canopy increased from 0·028 to 0·171 as average wind speed above the canopy for periods of high C increased from 1·7 to 3·6 m s^?1. Variations of C_m and F_D with increasing disease were well described (P < 0·0001) by a log‐normal model with 15% as the threshold above which C_m and F_D decreased as disease severity increased. These results indicate that disease severity should be used to adjust sporangia escape in spore transport simulation models that are used to predict the risk of spread of cucurbit downy mildew.     

Influence of fungicidal control of cucumber and tomato grey mould (Botrytis cinerea) on fruit yield

The fungicides tebuconazole, tebuconazole + dichlofluanid, fenethanil, diethofencarb + carbendazim, and vinclozolin combined with chlorothalonil were tested for their ability to control grey mould (Botrytis cinerea Pers. ex Fr.) of cucumber and tomato grey mould in greenhouses under commercial conditions. In winter 1987/88 the number of diseased female fruits of cucumber (Cucumis sativus L.) was reduced by diethofencarb + carbendazim (2·5 mg dm^?3 each) by 93% and by tebuconazole (2·5 mg dm^?3)(phytotoxic when alone) or tebuconazole (1 mg dm^?3) + dichlofluanid (4 mg dm^?3) by 54–57%. Vinclozolin (5 mg dm^?3) + chlorothalonil (25 mg dm^?3) significantly reduced disease incidence on fruits by 40%. Infection foci on cucumber stems were significantly decreased by vinclozolin + chlorothalonil. A more pronounced decrease was obtained with diethofencarb + carbendazim, tebuconazole, or tebuconazole + dichlofluanid. During the season of winter 1988/89, tebuconazole + dichlofluanid (1·5 + 6 and 3 + 12 mg dm^?3) and RH7592 (1 mg dm^?3) significantly reduced diseased fruits by 30–71%. Grey mould of tomato (Lycopersicon esculentum Mill.) leaves was reduced by more than 90% and on fruits by 78–87% when tebuconazole + dichlofluanid (1·5 + 6 and 3 + 12 mg dm^?3) or diethofencarb + carbendazim (2·5 mg dm^?3 each) were applied. Yields of cucumber fruits of the common parthenocarpic cv. Kasem 292 were weighed. There was no correlation between disease level and yield in any experiment, plot or date except for two measurements. Compesation in fruit production by the plant may be regarded as the reason for no positive yield response to efficient control. The possibility of reducing fungicide application is discussed. Control of grey mould on tomato resulted in yield increase.     

The role of pendimethalin in the integrated management of propanil-resistant Echinochloa colona in Central America

Pre-emergence activity of pendimethalin on propanil-resistant jungle rice (Echinochloa colona) was demonstrated in glasshouse trials. Both susceptible and resistant populations, collected from Costa Rica, were controlled by 1·25 kg ha^-1, the usual application rate used in the field where Rottboellia cochinchinensis is also a problem. When applied post-emergence, propanil performance was improved by the addition of low doses of pendimethalin to the herbicide mixture. A propanil-resistant selection was controlled by 0·23 kg ha^-1 pendi-methalin+0·54 kg ha^-1 propanil at the one-to-two leaf stage, and 0·23 kg ha^-1 pendimethalin+1·08 kg propanil at the three-to-four leaf stage compared to 1·08 kg and 2·16 kg ha^-1 respectively when propanil was applied alone. This suggests that pendimethalin improves post-emergence control in the field compared to the standard propanil treatment and can provide residual pre-emergence control of late-germinating individuals, so reducing the propanil selection pressure. For effective jungle rice control, growers apply propanil (3·84 kg ha^-1) at 10 and 20 days after planting (DAP) followed by one application of fenoxaprop-P-ethyl (0·045 kg ha^-1) at 35 DAP. Field experiments, conducted in dry-seeded upland rice in southern Costa Rica, demonstrated that under high jungle-rice population pressure, one application of pendimethalin at 1·5 kg ha^-1 provided an effective replacement for propanil, resulting in reduced weed-control costs. ©1997 SCI     

Soybean weed control by chloramben granules coated with haloxyfop-methyl

Experimental granules were made from moistened calcareous loess (pH 8·5) containing 2% w/w gum xanthan and chloramben sodium salt at w/w concentrations of 0·4–3·6%. Haloxyfopmethyl * * Approved WSSA common name.
(DOWCO-453 ME) {Methyl 2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)-phenoxy)propanoate) was dissolved in tung oil at a range of concentrations and poured on the dried chloramben granules with stirring. In the glasshouse, dry granules containing chloramben plus haloxyfop-methyl spread pre-emergence at the rate of 0·8 + 0·4 kg ha^?1 reduced the dry weight of maize (Zea mays L.), red rice (Oryza sativa L.), Abutilon theophrasti Medic., and Sesbania exaltata (Raf.) Cory by 89, 100, 94, and 68%, respectively, with no injury to soybeans [Glycine max (L.) Merr.]. Coated granules spread pre-emergence controlled A. theophrasti and volunteer maize grown from seed sown in soil up to 10 cm deep. In a preliminary field test, the experimental granules reduced numbers of weeds in soybeans and improved crop yield. Ten weeks after treatment, chloramben granules coated with haloxyfop-methyl gave 97% control of Sorghum halepense (L.) Pers compared to 80% by uncoated granules. Linuron granules coated with haloxyfop-methyl gave 85% control compared to 12% by uncoated granules. Yields in plots treated with coated and uncoated chloramben were 3280 and 2700 kg ha^?1, respectively. In coated and uncoated linuron plots, yields were 2920 and 2340 kg ha^?1, respectively. Except for the uncoated linuron plot, all yields were significantly higher than 2050 kg ha^?1 obtained in the weedy untreated plot.     

Characterization and Inhibitor Studies of Chitinases from a Parasitic Blowfly (Lucilia cuprina), a Tick (Boophilus microplus), an Intestinal Nematode (Haemonchus contortus) and a Bean (Phaseolus vulgaris)

The molecular weight pattern and the stage-specific activities of chitinases from the blowfly Lucilia cuprina, the tick Boophilus microplus and the intestinal nematode Haemonchus contortus were examined. Chitinolytic enzymes could be detected in all parasite species tested, but the activity was different between the stages. Highest chitinolytic titers were found in blowfly pupae (83 kDa, 118 kDa), hatching larvae of ticks (58 kDa, 94 kDa) and nematode eggs (43 kDa). Leaves from ethylene-treated bean plants Phaseolus vulgaris expressed two basic Class I chitinases (Ia, Ib) of 34 kDa, differing in their amino acid sequences at residue 33 and 34 (Ia: glycine, proline; Ib: lysine, aspartic acid). Inhibitor studies with blowfly pupae revealed that allosamidin (IC₅₀=0·32 (±0·02) μM ) was by far the best inhibitor when compared with various amino sugar derivatives. This compound also inhibited chitinases from tick larvae (IC₅₀=0·69(±0·10) μM ) and nematode eggs (IC₅₀=0·048(±0·0045) μM ) specifically. Whereas Class Ia chitinase from bean leaves was inhibited only up to 18% by 10 μM allosamidin, it had an IC₅₀ of 1(±0·14) μM for the Ib type, which is the first plant chitinase described to be highly sensitive to allosamidin.     

Screening Test for Insecticides Interfering with Cuticular Sclerotization

The potential of known and new insecticides to interfere with cuticle sclerotization was investigated using assays for key enzymes such as phenoloxidase, quinone methide isomerase and DOPA decarboxylase. Homogenates from the blowfly Lucilia cuprina and from the epithelial cell line from Chironomus tentans were used to examine the compounds under investigation. Phenoloxidases are known to oxidize DOPA, the substrate for DOPA decarboxylase. Since phenoloxidases were not detectable in C. tentans cell homogenates, inhibitor and kinetic studies were done for comparison with DOPA decarboxylase of this insect cell line. DOPA decarboxylase and phenoloxidase of L. cuprina exerted highest specific activities at early pupal stages (day 7). The apparent K_m values for the two enzymes were 0·47(±0·21) mM and 0·71(±0·16) mM , respectively, using L -DOPA as substrate. DOPA decarboxylase from C. tentans had a K_m value of 0·42(±0·18) mM . Quinone methide isomerase was most active in young pupae. In terms of substrate specificity for enzymic (mushroom-tyrosinase) production of different quinones from their corresponding catechols, that with dopamine quinone proved to be the most efficient. Synthesis of derivatives of L -DOPA and L -tyrosine led to a compound which inhibited both phenoloxidase and quinone methide isomerase. DOPA decarboxylase from L. cuprina and from cells of C. tentans was inhibited by carbidopa (IC₅₀ values of 0·021(±0·011) μM and 0·031(±0·019) μM , respectively) and indomethacine (IC₅₀ values of 22·6(±7·1) μM and 18·8(±9·7) μM ). Both compounds exerted a competitive type of inhibition and were able to interfere with development of L. cuprina.     

Genetic diversity, aggressiveness and metalaxyl sensitivity of Pythium aphanidermatum populations infecting cucumber in Oman

Seventy three isolates of Pythium aphanidermatum obtained from cucumber from four different regions of Oman and 16 isolates of muskmelon from the Batinah region in Oman were characterized for aggressiveness, sensitivity to metalaxyl and genetic diversity using AFLP fingerprinting. Twenty isolates of P. aphanidermatum from diverse hosts from different countries were also included in the study. Most isolates from Oman were found to be aggressive on cucumber seedlings and all were highly sensitive to metalaxyl (EC₅₀ < 0·80 µg mL^?1). Isolates from cucumber and muskmelon were as aggressive as each other on both hosts (P > 0·05), which implies a lack of host specialization in P. aphanidermatum on these two hosts in Oman. AFLP analysis of all isolates using four primer–pair combinations resolved 152 bands, of which 61 (~40%) were polymorphic. Isolates of P. aphanidermatum from Oman and other countries exhibited high genetic similarity (mean = 94·1%) and produced 59 different AFLP profiles. Analysis of molecular variance indicated that most AFLP variation among populations of P. aphanidermatum in Oman was associated with geographical regions (F_ST = 0·118; P < 0·0001), not hosts (F_ST = –0·004; P = 0·4323). These data were supported by the high rate of recovery (24%) of identical phenotypes between cucumber and muskmelon fields in the same region as compared to the low recovery (10%) across regions in Oman, which suggests more frequent movement of Pythium inoculum among muskmelon and cucumber fields in the same region compared to movement across geographically separated regions. However, recovering clones among regions and different countries may imply circulation of Pythium inoculum via common sources in Oman and also intercontinental spread of isolates.     

Baseline and differential sensitivity of Peronophythora litchii (lychee downy blight) to three carboxylic acid amide fungicides

Downy blight, caused by Peronophythora litchii, is an important disease of lychee (litchi) plants in China. The in vitro sensitivities of various asexual stages of P. litchii to the three carboxylic acid amide (CAA) fungicides dimethomorph, flumorph and pyrimorph were studied with four single‐sporangium isolates. None of the three fungicides affected zoospore discharge from sporangia, but they strongly inhibited mycelial growth (mean EC₅₀ values of 0·075, 0·258 and 0·115 mg L^?1, respectively); sporangial production (mean EC₅₀ values of 0·085, 0·315 and 0·150 mg L^?1, respectively); germination of cystospores (mean EC₅₀ values of 0·140, 0·150 and 0·645 mg L^?1, respectively); and germination of sporangia (mean EC₅₀ values of 0·203, 0·5 and 0·743 mg L^?1, respectively). As mycelial growth was the most sensitive stage to dimethomorph and pyrimorph, it was chosen to test baseline sensitivities to the three fungicides. In 2007, from 131 isolates collected in Fujian, Guangdong and Guangxi provinces, 127, 116 and 113 isolates were used to establish baseline sensitivity for dimethomorph, flumorph and pyrimorph respectively. Isolates from different provinces exhibited similar baseline sensitivity to the same fungicide. Baseline sensitivities to dimethomorph, flumorph and pyrimorph were distributed as unimodal curves, with mean EC₅₀ values of 0·082 (± 0·01), 0·282 (± 0·047), and 0·115 (± 0·032) mg L^?1, respectively. This information will serve as a baseline for tracking future changes in sensitivities of P. litchii populations to these three CAA fungicides.     

An Insecticidal and Acaricidal Polysulfide Metabolite from the Roots of Petiveria alliacea

The present study reports on the insecticidal and acaricidal potentials of dibenzyltrisulfide (DBTS) isolated from the roots of Petiveria alliacea L. using thin layer and high performance liquid chromatography. The 96-h LD₅₀ value (μg per tick) obtained for adult Boophilus microplus (Canestrini) topically treated with DBTS was 0·920. The LD₅₀ values obtained for three commercial acaricides dimethoate, lindane and carbaryl were 4·6, 9·3 and 6·9 μg per tick respectively. The IOD₅₀ and IHD₅₀ (concentrations inhibiting egg laying and hatching by 50% respectively) in μg per tick doses for DBTS were 0·22 and 0·24 respectively. The 24-h LD₅₀ dose (μg per insect) obtained for DBTS on adult Cylas formicarius elegantulus (Summer) was 0·193 μg per insect. The vapour from a stock solution of 5 g litre^-1 of DBTS was highly toxic to adult Hypothenemus hampei Ferr. inside coffee berries, inflicting 89% mortality within 24 h. © 1997 SCI.     

Biocontrol of sclerotinia stem rot (Sclerotinia sclerotiorum) of soybean using novel Bacillus subtilis strain SB24 under control conditions

Sclerotinia stem rot (SSR), caused by Sclerotinia sclerotiorum, is a major disease of soybean in Canada. Laboratory and greenhouse experiments were conducted to evaluate potential effectiveness of cell suspensions, cell‐free culture filtrates and broth cultures of Bacillus subtilis strain SB24 for suppression of SSR. The SB24 cell suspensions and cell‐free culture filtrates significantly reduced mycelial growth of S. sclerotiorum by 50 to 75% and suppressed sclerotial formation by > 90%. The severity on soybean was negatively correlated (r < ?0·84, P < 0·01) to the concentrations of cell suspension, cell‐free culture filtrate and broth culture applied. The cell suspension and broth culture preparations significantly (P < 0·01) reduced SSR severity by 45 to 90% at concentrations ranging from 5 × 10⁶ to 10⁹ CFU mL^?1. The most effective concentration was 5 × 10⁸ CFU mL^?1 for all three preparations, reducing the severity by 60 to 90%. The B. subtilis SB24 was most effective in reducing disease severity when applied ≤ 24 h before plant inoculation with S. sclerotiorum and a significant effectiveness was observed up to 15 days after plant inoculation. The population density of B. subtilis on soybean leaves decreased by 1·5 to 2·5 log units over 15 days under field conditions, and by 0·8 log units over 5 weeks under control conditions. The decrease in population density was significantly correlated with rainfall in the field (r < ?0·93, P < 0·01), suggesting that the biocontrol bacteria may be washed away by rain.