A study of the effects of fungitoxic compounds on Phytophthora cinnamomi in water

Copper and chlorine-releasing compounds were the most fungitoxic of 13 compounds tested in water for inhibition of Phytophthora cinnamomi. Mycelium was killed when immersed for 24 h in suspensions containing copper (13–45 mg/1) or a solution containing free residual chlorine (100 mg/1). Sub-lethal concentrations of these compounds reduced the numbers of sporangia. Exposing zoospores of P. cinnamomi for 60 s to water containing 2 mg free residual chlorine/1 reduced subsequent colony production on agar plates by 96–100%.
Prothiocarb, etridiazole ex. and furalaxyl killed mycelium immersed in solutions or suspensions for 3–6 days at 1500, 1000 and 600 mg a.i./l respectively and suppressed sporangium production at 1000, 500 and 300 mg/1.
Mycelium survived 3 days' immersion in ethyl hydrogen phosphonate compounds at 4000 mg a.i./l but 1000 mg a.i./l suppressed sporangium formation.
1-(2-Cyano-2-methoxyiminoacetyl)-3-ethyl urea and drazoxolon did not kill mycelium at 2000 and 1500 mg a.i./l respectively with a 6-day exposure, but reduced numbers of sporangia produced.     

The suppression of Phytophthora syringae in orchard soil by furalaxyl as a means of controlling fruit rot of apple and pear

Apple orchard soil treated with Aaterra (etridiazole), A5430 (furalaxyl), copper sulphate, LS 74–783 (aluminium tris(ethyl phosphonate)) or water in mid-August 1977 was assayed for Phytophthora syringae by an apple fruit baiting method immediately after fungicide application and at weekly intervals for 8 wk. There was no infection of baits placed in the orchard and this was attributed to low rainfall. When wetted and baited, samples of surface soil caused from 0 to 85% fruit infection depending on the time of sampling and soil treatment. In control soil, fungus activity was low in the first 4 wk, high in the fifth wk and fluctuated widely thereafter. In samples from soils treated with Aaterra, copper sulphate or LS 74–783 activity was first apparent in the fifth wk and then fluctuated roughly in parallel with that of control soil although at generally lower levels. Changing levels of activity were apparently related to air temperature during baiting. No infection of fruits occurred in any samples from soil treated with furalaxyl. Further assays of this soil indicated a complete suppression of P. syringae to at least 10 cm soil depth. Furalaxyl is sufficiently active to be considered as a soil treatment for controlling Phytophthora fruit rot of apple and pear.     

Greenhouse and field evaluations of potassium phosphonate: the control of Phytophthora foot rot of black pepper in Vietnam

Phytophthora foot rot of black pepper caused by Phytophthora capsici is a major disease of black pepper throughout production areas in Vietnam. The disease causes collar, foot and tap root rots and eventual death of the infected vine. Potassium phosphonate was evaluated for the control of this disease in greenhouse and field trials. In greenhouse trials three-month-old vines treated with phosphonate by soil drenching (10–20 g a.i./l) and then inoculated with P. capsici mycelium (2% v/v soil) had significantly less foot rot compared to vines grown in non-treated soil. In field trials mature vines were treated with phosphonate at 50–100 g a.i/pole soil drenching or 10 g a.i./l by root infusion. After 10 days root, stem and leaf specimens were removed for bioassay by inoculation with 5 ml of P. capsici zoospores suspension (10⁶–10⁸ spores/ml). Soil drenching with phosphonate inhibited the colonisation of pathogen on excised leaf, stem and root tissues, significantly more than phosphonate root infusion. Our study provides further evidence supporting the efficacy of potassium phosphonate in the management of black pepper foot rot caused by P. capsici. The excised leaf and stem bioassay used in this study is a rapid and useful technique for testing the efficacy of systemic fungicides in controlling this disease.     

The effect of Benlate and cytokinins on the content of tobacco mosaic virus in tomato leaf disks and cucumber mosaic virus in cucumber cotyledon disks and seedlings

Tomato leaf disks were inoculated with tobacco mosaic virus (TMV) and floated for 7 days on solutions of kinetin and benzyladenine in the range 20-0-002 mg/1. Virus content was reduced at the higher and increased at the lower concentrations. Benlate and benomyl showed a peak of cytokinin activity in the Amaranthus betacyanin bioassay equivalent to c. 0–002 fig/l kinetin. At concentrations above 25 and 100 mg a.i./l for Benlate and benomyl respectively, both compounds increased the TMV content of tomato leaf disks. Cucumber mosaic virus (CMV) content in cucumber cotyledon disks was increased by Benlate and benomyl treatment (50–100 mg/1). Applied as a soil drench (50–500 mg a.i./l) when the plants were inoculated, Benlate increased the CMV content of infected seedlings. The number of starch-iodide lesions (a measure of susceptibility) was unaltered in cotyledons treated with Benlate 7 days before or immediately after inoculation. Infectivity of crude infective cucumber sap was unaffected by benomyl incorporation, whereas Benlate reduced infectivity at higher concentrations (1000–5000 mg/1). Under the experimental conditions described, Benlate, benomyl, benzyladenine and kinetin had no effect on the chlorophyll content of tomato leaf disks, and intact seedlings.     

Physiological studies of a hybrid between populations of Dactylis glomerata from contrasting climatic regions. II. Intra population variation

Mushroom compost was treated with nematicides and infested with Aphelenchoides composticola at the time of filling into growing containers. Yields of mushrooms from infested untreated control composts were reduced to 40–60% of yields from uninfested control compost. Yields from infested compost treated with fenamiphos emulsifiable concentrate (e.c.) at 10 or 20 mg a.i./kg, thiabendazole wettable powder at 40 or 60 mg a.i./kg or oxamyl granules at 20 mg a.i./kg were as high as from uninfested controls. Compost treated with granules of AC 64,475 up to 20 mg a.i./kg or ethoprophos or thionazin up to 80 mg a.i./kg gave yields significantly lower than uninfested controls. Numbers of nematodes rose to about 10⁶/20 g of compost in untreated compost and then fell, and a similar peak occurred in treatments in which yields were substantially reduced by nematode damage. Treatments which yielded as well as the uninfested controls held maximum nematode numbers down to about 10V20 g of compost but populations stayed at this level or tended to rise while numbers in untreated compost fell. Incorporation of fenamiphos in casing or its application to the surface of beds 3 wk after cropping began gave lower yields than the uninfested control but mushrooms were being produced late in the cropping cycle. Fenamiphos e.c. at 20 mg ai./kg incorporated in compost is considered a practical preventive measure for control of A. composticola.     

Isolation and Identification of Pythiaceous Fungi from Irrigation Water and their Pathogenicity to Antirrhinum, Tomato and Chamaecyparis lawsoniana

Pythiaceous fungi were isolated from irrigation water using a variety of natural and artificial baits. Isolates were also obtained by plating water samples directly on the surface of selective agar media. The selective medium of Ocana and Tsaq (1966) PlOVP, was modified by substituting rifampicin and ampicillin (10 and 500 μg cm^?3 respectively) for vancomycin to suppress bacterial growth from water samples. The pythiaceous fungi were identified as Pythiitm dissotocitm, P. middletonii, P. mamillatum, P. rostratum, Pythium“group 1”, “group 2” and “group 3” and Phytophtbom gona-podyides. All isolates of P. gonapodyides were the A1 strain and produced oospores when paired with an A2 isolate of P. drechsleri. Isolates were tested for their pathogenicity to Antirrhinum, tomato and Chatmaecyparis lawsoniana cv. Ellwoodii. Pythium middletonii and Pythium“group 1” caused severe pre-emergence damping-off of Antirrhinum seedlings, P. mamillatuni, P. rostratum and Pythium“group 3” were less pathogenic to the same host while P. dissotocum, Pythium“group 2” and Phytophthora gonapodyides were non-pathogenic. Only isolates of Pythium“group 1” were pathogenic to tomato seedlings. None of the fungi was pathogenic to rooted cuttings of Chamaecyparis lawsoniana cv. Ellwoodii.     

A small-scale screening technique for evaluating fungicides against Phytophthora palmivora pod rot of cocoa

Plots of clonal Trinitario cocoa were sprayed with fungicides in the field. Ripe pods were harvested from the trial plots and artificially inoculated with Phytophthora palmivora using various techniques, the most suitable of which proved to be the zoospore spot method. Percentage infection results from the spot inoculation tests agreed well with the field percentage infection results and it was concluded that field spraying followed by zoospore spot inoculation of detached pods is a suitable preliminary screening technique for fungicides. Three systemic fungicides metalaxyl, aluminium tris (ethyl phosphonate) and DPX-3217 in a mixture with captafol and copper oxychloride were compared with the protectant cuprous oxide. Metalaxyl was found to be the most effective of the systemic fungicides and when applied at the rate of 0·44 g ai/ha every 8 wk it gave a similar reduction in percentage infection to 4 weekly applications of cuprous oxide at the rate of 4·4 kg Cu⁺⁺/ha during the wetter part of the year when pod rot is most severe.     

Studies on the biodegradation of nonionic surfactants applied in the polyestre fibre industry. III. Effect of adaptation on the respiratory activity of organisms and on the biocenosis of inoculated sludge.

Manometric studies were conducted in 3 series. In the first one the sludge used for inoculation was non adapted to water purification containing surfactants. In the second and third series it was adapted to the sludge load 0.11 and 0.28 mg surfactant/mg d.w./day respectively. Increase in oxygen uptake was proportional to the degree of the adaptation of microorganisms only within limited range of surfactant concentration not exceeding 500 mg/l for Cirrasol FP and 1000 mg/l for Cirrasol SF and Cirrasol TCS. The toxic action of surfactants against Ciliata was noted at concentration above 100 mg/l and for Mastigota and Sarcodina above 500 mg/l, even by using adapted sludge for inoculation.     

Centrin association with the flagellar apparatus in spores ofPhytophthora cinnamomi

Summary Antibodies raised against the calcium-binding protein centrin, were used to identify and localise centrin containing structures in the flagellar apparatus of zoospores and cysts of the oomycetePhytophthora cinnamomi. Immunoblotting of extracts from zoospores indicates that theP. cinnamomi centrin homologue is a 20 kDa protein. Immunofluorescence microscopy with anti-centrin antibodies reveals labelling in the flagella, the basal body connector and co-localisation along the microtubular R1 root (formerly called AR3) that runs from the right side of the basal body of the anterior flagellum into the anterior of the zoospore close to the ventral surface. The centrin (R1^cen) and tubulin components of the R1 root split into four loops on the right hand side of the ventral groove and rejoin along the left hand side of the groove. The R1 root continues down the left hand side of the zoospore past the basal bodies and parallel to the R4 root. We propose that at least inP. cinnamomi there is no R2 root. Immunogold labelling confirms that centrin is a component of the basal body connector complex. When the zoospores become spherical during encystment, the R1^cen pivots by approximately 90 ° with respect to the nucleus.     

The effect of the weight of the seedling-derived tuber on subsequent clonal generations in a potato breeding programme

Cultures of Polymyxa graminis were maintained in roots of barley plants grown in sand at different temperatures using Wisconsin soil temperature tanks. At 17 – 20°C, the minimum time from inoculation with cystosori to the production of zoospores from the inoculated roots was 2 – 3 wk. At 11 – 20°C many zoospores were produced but the incubation period was longer at the lower temperatures. Above 20°C little fungal development occurred. The duration of motility of zoospores ranged from c. 1 h to > 24 h. Bovine serum albumen (BSA) prolonged motility but glycine and glucose had no effect or, at higher concentrations, were toxic. Zoospores were rapidly immobilised by zinc ions in solution at or above 10μg/ml. In some experiments BSA added to the zoospore suspension greatly increased transmission of barley yellow mosaic virus (BaYMV) while glucose, glycine and ovalbumen decreased it. When seedlings were incubated with zoospore suspensions for 24 h at different temperatures, BaYMV transmission was high (> 60%) at 10, 15 and 20°C but there was little at 5 or 25°C. In experiments to determine the time taken for zoospore penetration, seedlings were incubated in suspension for different periods of time and then rinsed in zinc sulphate solution to kill free zoospores. Between 3 and 3·5 h was needed for zoospores to establish infection. Transmission occurred equally to plants of various ages between 3 days and 7·5 wk.     

The infection of apples by Phytophthora syringae

Contamination with infected soil has led to high wastage of apples in storage due to rotting by Phytophthora syringae. At 3-3 ^oC lesions formed 3–4 wk after inoculation with zoospores; the percentage infection fell if the suspensions dried after 48 h at this temperature and after 22 h at 15 ^oC. Infected soil rotted fruit only if kept moist; at 3-3 ^oC a 3-day period of wetness resulted in 37-5% rotting after 8 wk. Fruit dipped in soil slurry remained wet in some parts of a 4361(12 bushel) bin for at least 3 wk. There was a 10-fold increase in rotting by contact between sound and rotting fruit after 11 wk at 3-3 ^oC. Captan gave effective protection against rotting derived from zoospores or infected soil; it had no eradicant action.     

Synthesis,Characterization and Evaluation of Cytotoxic Activities of Novel Aziridinyl Phosphonic Acid Derivatives

New aziridine 2‐phosphonic acids were prepared by monohydrolysis of the aziridine 2‐phosphonates that were obtained by the modified Gabriel?Cromwell reaction of vinyl phosphonate or α‐tosylvinyl phosphonate with a primary amine or a chiral amine. The cellular cytotoxicity of these compounds was tested against the HCT‐116 colorectal cancer cell lines and the CCD‐18Co normal colon fibroblast lines using the MTT assay. Three of the synthesized phosphonic acid derivatives 2e (ethyl hydrogen {(2S)‐1‐[(1S)‐1‐(naphthalen‐2‐yl)ethyl]aziridin‐2‐yl}phosphonate), 2h (ethyl hydrogen (1‐benzylaziridin‐2‐yl)phosphonate), and 2i (ethyl hydrogen (1‐cyclohexylaziridin‐2‐yl)phosphonate) showed higher cytotoxicity than the reference cancer treatment agent etoposide. Cell death was through a robust induction of apoptosis even more effectively than etoposide, a well‐known apoptosis inducing agent.     

Benzoic acid induces tolerance to biotic stress caused by Phytophthora cinnamomi in Banksia attenuata

Banksia attenuata plants were treated with soil drenches or foliar sprays of benzoic acid (BZA) to determine induced resistance to Phytophthora cinnamomi. Stems of B. attenuata were inoculated with the pathogen 1 week after treatment with BZA. Resistance was estimated by measuring P. cinnamomi lesions on stems. Treatment with 0.10 mM, 0.25 mM or 0.50 mM BZA caused a reduction in lesion size with 0.50 mM BZA applied as a soil drench being the most effective treatment at suppressing the development of lesions. This is the first report of BZA induced host resistance in any plant species to any pathogen.     

Development of a dot immunobinding assay to detect Phytophthora spp. in naturally dark-rooted woody plants

An indirect dot immunobinding assay (DIBA) with a PAb raised against an isolate of P. cinnumomi was evaluated to detect Phytophthora spp. in naturally dark-rooted woody plants. Screening of different modifications of the procedure were done with root samples of Chamaecyparis lawsoniana non-infected and infected with P. cinnamomi. With the optimised DIBA procedure, root infection could be diagnosed by a clearly defined halo around the spot and by a colour change in the spot using Fast Red or Fast Blue substrate. Detection of different Phytophthora species in Chamaecyparis plants from commercial nurseries was successful with the optimised procedure.     

Comparison of fungicides for the control of Rhizoctonia solani causing datnping-off of mung bean (Phaseohis aureus)

Of 41 fungicides tested in the laboratory, copper carbonate, copper sulphate, mercuric chloride, Agrosan GN, quintozene, kasugamycin, carboxin, pyracar-bolid, carbendazim, chloroneb, benomyl, Ohric, RH 893 (2-n-octyl-4-isothiazole-3-one) and Terrazole were most inhibitory to the mycelial growth of Rhizoctonia solani on Czapek's agar plates and had EC₅₀ values of less than 1 μg a.i./ml, while copper oxychloride, Udonkor, zineb, ziram, F 319 (3-hydroxy-5-methyl isoxazole) and anilazine were much less toxic, ziram being least inhibitory with an EC₅₀ of 214 μg a.i./ml. Of 17 fungicides tested in the greenhouse as seed treatments, thiabendazole, carbendazim, benomyl, thiophanate-methyl, dichlozoline and Ohric gave 80–90% control of damping-off of mung bean seedlings. A single soil drench with thiophanate-methyl and two drenches with benomyl gave about 90% disease control, More seedlings with R. solani infection survived when thiophanate-methyl was used as a post-inoculation soil drench than when benomyl or chloroneb were used.     

Variability in the Sensitivity of Rhizoctonia solani Anastomosis Groups to Fungicides

Tolclofos-methyl, iprodione and cyproconazole, among the eleven fungicides tested in vitro, gave consistently strong inhibition against all ten anastomosis groups (AGs) of Rhizoctonia solani. Carboxin, furmecyclox, thiabendazole, fenpropimorph and vinclozolin also inhibited all AGs but with wide variations in toxicity levels (EC90 values). Pencycuron showed strong activity against four AGs but was ineffective against the other six AGs. Generally, R. solani AGs were insensitive to fenarimol and imazalil. Tolclofos-methyl strongly inhibited 23 AG2-1 and 20 AG4 rapeseed/canola R. solani isolates from different locations in Saskatchewan, Alberta and Manitoba. The same isolates were also sensitive to iprodione, cyproconazole and carboxin. All AG4 canola isolates were insensitive to pencycuron (EC90 > 500 mg/l) while AG2-1 isolates showed highly variable levels of sensitivity with EC90s ranging from 0.5 to 220 mg/l. Tolclofos-methyl, applied to Brassica napus (canola) cv. Westar seed at 1 g a.i./kg, provided 75—100 % control of seedling damping-off in pots infested with AG2-1 or AG4 isolates. In parallel experiments, pencycuron (1 g a.i./kg seed) failed to control damping-off by AG4 canola isolates and gave variable disease control against AG2-1 isolates.     

Variation in the sensitivity to metalaxyl of Pythium spp. isolated from carrot and other sources

Over a 3-yr period 261 isolates of 17 species of Pythium were tested for sensitivity to metalaxyl at concentrations of 5, 50 or 100 μ/ml. A wide range of responses was observed, from isolates where growth ceased at 5 μg/ml to those where growth at 100 μg/ml was similar to that of the untreated controls. In further tests isolates of 11 different species had ED50's < 1 μg/ml. A lower sensitivity was detected in isolates of six Pythium spp. where values in the range 1–10 μg/ml were obtained. This lower sensitivity was not related to previous known use of metalaxyl. Three isolates of Pythium dissotocum from sites where the fungicide had been used repeatedly had ED50's > 100 μg/ml and were considered resistant. The resistance was stable over a 2-yr period and isolates were cross-resistant to furalaxyl, benalaxyl, ofurace, cyprofuram and oxadixyl. Increasing concentrations of metalaxyl reduced or prevented the production of zoospores by four species of Pythium, although when zoospores were produced, this was followed by the normal processes of encystment and germination. Culturing P. dissotocum on different sub-lethal concentrations of metalaxyl for 18 wk did not induce a high level of resistance to the fungicide.     

The effect of benomyl on the infection of tomatoes by Fusarium oxysporum f.sp. lycopersici and Botrytis cinerea

In glasshouse experiments at Auchincruive, drench applications of benomyl (100 or 142 mg per plant) to the soil surface around the stem bases of pot-grown tomato plants before inoculation with Fusarium oxysporum f.sp. lycopersici reduced the penetration of the fungus up the stems and/or decreased the development of vascular discoloration and associated severity of wilting. Similar drenches applied after establishment of the fungus in the stems either halted or considerably retarded the growth of the pathogen up the vessels. This again was reflected in reduced vascular discoloration and wilt symptoms. In experiments with benomyl over 2 years at a commercial holding in Argyll, the application of soil drenches (at the rates above) shortly after planting out and again 5 weeks later, coupled with a programme of stem and foliar sprays (at 0–05 % a.i.) during the summer, reduced the development of stem lesions caused chiefly by Botrytis cinerea and increased the general survival of plants more than did drench or spray treatments alone. There were indications that ‘ghost spotting’ of the fruit, particularly where spray applications were made, was also slightly reduced, but the magnitude of the effect was not consistent.     

Effect of Post-infection Application of Fungicides on the Apple Scab Pathogen, Venturia inaequalis (Cke.) Wint.

The Ergosterol-biosynthesis inhibiting (EBI) fungicides had a prolonged inhibitory effect on the growth and sporulation of the fungus, Venturia inaequalis thereby preventing development of typical apple scab symptoms. Atypical lesions in the form of chlorotic or reddish brown flecks had reduced viable sporulation with deleterious effect on subcuticular hyphae when fungicide was applied beyond 144 h but before 170h after inoculation. Myclobutanil (45μg a.i./ml) had the maximum inhibitory effect on sporulation and colony growth while bitertanol (187.50 μg a.i./ml) showed only a temporary inhibition of fungal growth and sporulation. Ultra-structural studies also exhibited different levels of fungitoxicity by different fungicides when applied 144 h after inoculation.