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1.
Exposure of sclerotia of Macrophomina phaseolina to 0 and 33% relative humidity (r.h.) for 12 weeks and of Sclerotium cepivorum to 0, 33 and 55% r.h. for 20 weeks did not reduce their germinability on agar. Exposure to 78% r.h. caused high loss of germinability in M. phaseolina and complete loss in S. cepivorum. After 7-day exposures respective moisture contents of sclerotia of M. phaseolina and S. cepivorum were 1 and 2% at 0% r.h.; and 10 and 14% at 78% r.h. M. phaseolina sclerotia held at 0% and 33% r.h. in desiccators for several times up to 12 days did not decrease in subsequent survivability in moist soil, unlike sclerotia held at 78% r.h. for 4 days.More sclerotia of M. phaseolina were colonized by fungi and Streptomyces spp. on alkaline soil than on acid soil. On alkaline soil twice as many sclerotia were colonized after exposure to 0% r.h. as after exposure to 33, 55 and 78% r.h. Colonization of S. cepivorum sclerotia was as high on acid as on alkaline soil and 3 times as high on sclerotia treated at 0% r.h. as on those treated at higher r.h. Attempts to ascertain the effects of colonization on sclerotial viability were unsuccessful. Incubation of sclerotia of M. phaseolina in moist Rumsford sandy loam (50% m.h.c.) for 20 weeks reduced survivability by 43%. At room temperature, alternate drying and wetting of soil containing sclerotia did not appreciably affect survivability of either pathogen. Survivability of S. cepivorum sclerotia was highest when the sclerotia were incubated in air-dried soil (2–3% m.h.c.) for 20 weeks.Incidence of white rot on onion seedlings transplanted to S. cepivorum-infested soil was higher in soil that had been air-dried for 20 weeks than in soil that had been alternately wetted and dried. Sclerotia that were exposed to 0% r.h. for 7 days before soil incubation produced little white rot.  相似文献   

2.
Mulching of Sclerotium oryzae infested soil (moist or dry) with polyethylene sheets during hot summer days of May and June increased the soil temperature at 5 cm from 36°C (unmulched) to 48°C (wet) and from 44 to 52°C (dry) and at 20cm from 32 to 38°C (wet) and from 35 to 39°C (dry). In artificially-infested soil, the sclerotia were not eradicated but 95–100% loss in viability was observed at 5 cm by a mulch treatment for 1 week and at 20 cm by mulching for 8 weeks. Mulching effects were not influenced by moisture content of soil or by amendments with lucerne or wheat straw. Mulching of naturally-infested soil at a second site did not eradicate S. oryzae but reduced sclerotial viability by 93%.  相似文献   

3.
The proportion of viable sclerotia of Sclerotium cepivorum placed in field plots in Burnaby, British Columbia, decreased with time (P = 0.05). Sclerotia that had been air-dried for 48–72 hr had a lower percentage survival than those that had not been dried. Sclerotia placed on the soil surface decayed more rapidly than those buried at 15 cm (P = 0.05). Loss of viability was due to decay of sclerotia rather than to a reduction in the ability of the sclerotia to germinate which did not decline with time (P = 0.05). After 16 months in the field 23.6; 2.1; 11.7 and 8.9% of the sclerotia remained viable in the not-dried buried, not-dried surface, dried buried and dried surface treatments respectively.  相似文献   

4.
Mulching of Macrophomina phaseolina-inksted soil (moist or dry) with transparent polyethylene sheets during the hot days of May increased temperature of wet soil at 5 cm from 37°C (unmulched) to 52°C (mulched) and of dry soil from 52°C (unmulched) to 65°C (mulched). At 20 cm mulching increased temperature from 30°C to 41°C (wet) and from 38°C to 42°C (dry). In artificially-infested soil. the sclerotia of M. phaseolina were eradicated at 5 cm by a mulch treatment for 1 week and at 20 cm depth 50% sclerotia lost viability in wet soil but were not affected in dry soil. In a naturally infested soil (5–7 sclerotia g?1), which gave 20% infection on Vigna, the sclerotia were reduced to such an extent that after 1 week mulching no disease was observed on Vigna.  相似文献   

5.
At least 75% of the sclerotia of Macrophomina phaseolina survived for 1 yr in most natural soils kept at 26°C and at 50–55% of the soil moisture holding capacity (m.h.c.). Although survivability was reduced in a very acid soil (pH 4.5) collected under a pine stand, 33% of the sclerotia survived for 1 yr. Soil pH had very little or no effect on sclerotial survivability. Of three organic amendments tested (alfalfa hay, chitin, pine needles) only ground alfalfa hay at 0.8% (w/w) reduced survivability of sclerotia in soil by about 75% in a year. Alfalfa hay at 0.4% reduced survivability by 36%. Various N sources added at 200 μg Ng?1 soil had no effect on survival. Of 13 fungicides tested, only benomyl and captan at 20 μg a.i. g?1 soil appreciably reduced populations of sclerotia in soil.Soil temperature and moisture content were the two most important factors affecting survivability of sclerotia. At ?5 or 5°C the biggest drop in sclerotial survivability occurred when the soil was incubated moist (at 50% m.h.c. or more). At 26°C the biggest drop occurred in air-dried soil (2–3% m.h.c.) and survivability was decreased to some extent at 15 and 30% m.h.c. Survivability also dropped rapidly in moist soil (50–55% m.h.c.) exposed to four cycles each having 3-week freezing (?5°C) and 1 week thawing (26°C). Sclerotia in air-dried soil (2–3% m.h.c.) continuously kept at ?5°C maintained nearly complete survivability after 16 weeks. Sclerotia survived almost 80–90% in moist soil (50–55% m.h.c.) kept for 16 weeks at 26°C or in moist soil exposed to four cycles each having 3-week thawing (26°C) and 1-week freezing (?5°C).  相似文献   

6.
Nutrient independent conidia of Cochliobolus victoriae and sclerotia of Sclerotium cepivorum, Macrophomina phaseolina, and Verticillium dahliae were incubated aseptically on sand through which a dilute salts solution percolated at a flow rate sufficient to inhibit germination. Propagules were then transferred to a static salts solution to assess germination. Conidia of C. victoriae and sclerotia of S cepivorum became nutrient-dependent (6% germination in salts solution) after 9 and 15 days on sand, respectively. Thirty-five days of diffusive stress were required to attenuate the nutrient-independence of M. phaseolina sclerotia. Sclerotia of V. dahliae lost little of their nutrient-independence even after 45 days of diffusive stress. Viability of C. victoriae and S. cepivorum was reduced after 45 days of diffusive stress, but viability of V. dahliae and M. phaseolina was not. Conidia of C. victoriae gradually became nutrient-dependent when incubated for several weeks on each of five soils. A loam and two sandy loam soils were more effective in decreasing the nutrient-independence of conidia than were two clay loams. Sclerotia of M. phaseolina also lost nutrient-independence when incubated on four of the five soils.Interruption of artificially imposed diffusive stress resulted in increased [14C]exudation from conidia of C. victoriae and sclerotia of M. phaseolina. Germinability on salts solution of C. victoriae conidia previously made nutrient-dependent was significantly increased, when the conidia were kept at 4°C for 3.5 days before germination assay. Conidia of C. victoriae made nutrient-dependent and then incubated on soils labeled with [14C]glucose, absorbed twice as much 14C from a loam and two sandy loam soils as from two clay loam soils. Following incubation on four of the five 14C-labeled soils, the germinability of the conidia in the absence of nutrients was significantly increased over that of conidia not incubated on these soils.The results suggest that a continued minimal stress may be needed to maintain the nutrient-dependence of some fungal propagules in soil. Interruption of nutrient stress appears to allow nutrient-dependent propagules an opportunity to recoup nutrients from the soil solution or to reorganize endogenous energy reserves whereby the potential for germination is increased.  相似文献   

7.
The viability of sclerotia of Sclerotium oryzae was tested in both wet and dry soil under simulated elevated temperatures in either constant, cyclic or short temperature regimes. In wet soil viability was reduced to zero by a constant temperature of 45°C and above for 1 day or a minimum oven temperature of 55°C for 2 h. Viability of sclerotia were destroyed by either a 10-day constant temperature of 40°C or a 2-h temperature cycle for 3 days at 50°C or 12 days at 45°C. Below 40°C sclerotia were not affected. In dry soil at 60°C, a 3-day constant temperature or a 12 days 2-h temperature cycle eliminated sclerotial viability. Data on time and temperature relationships on loss in viability of sclerotia in soil could thus be used to predict efficacy of soil solarization.  相似文献   

8.
The effect of covering soil with transparent polyethylene sheets, known as soil solarization, on the viability of plant pathogens was determined. The treatment was tested in mid-summer on sandy loams in N.W. and S. Victoria. Columns of moist soil were inoculated with one of a variety of pathogens, viz. Fusarium oxysporum, Pythium irregulare, Plasmodiophora brassicae, Sclerotium cepivorum, S. rolfsii, Sclerotinia minor, Verticillium dahliae and the nematodes Macroposthania xenoplax, Meloidogyne javanica, Pratylenchus penetrans and Tylenchulus semipenetrans. Columns were placed vertically in soil, and then treated either for 4 weeks in N.W. Victoria, or 6 weeks in S. Victoria.Preliminary laboratory tests showed that pathogens were killed by temperatures within the range 38–55°C. The relative sensitivities of pathogens to fluctuating soil temperatures were similar at both sites. The most sensitive were the nematodes, and the fungi V. dahliae, S. cepivorum and S. minor, while F. oxysporum, P. irregulare and P. brassicae were the least sensitive. In N.W. Victoria treatment effects were apparent to 26 cm and most pathogens were not recovered from 0 to 11 cm. In S. Victoria treatment effects were apparent to a depth of 16cm and most pathogens were not recovered from 0 to 6cm.  相似文献   

9.
Germinability and virulence of sclerotia of Sclerotium rolfsii were assessed after 50 days of exposure of 14C-labeled sclerotia to soil at 0, −5 and −15 kPa and pH 6.9, or to soil at 15, 25 or 30 °C, pH 5 or 8 and −1 kPa. Evolution of 14CO2 accounted for the greatest share of endogenous carbon loss from sclerotia under all soil conditions, except in water-saturated soil (0 kPa), in which sclerotial exudates contributed the major share of carbon loss. Total evolution of 14CO2 from sclerotia in soil at −15 kPa (42.4% of total 14C) and at −5 kPa (38%) was significantly higher than at 0 kPa (23.8%). Evolution of 14CO2 in soil at 25 or 30 °C was more rapid than at 15 °C with regardless of pH. Loss of endogenous carbon by sclerotia was the greater after 50 days of exposure to soil at 0 kPa, or at 25 or 30 °C and pH 8, than at other soil conditions. Sclerotia exposed to water-saturated soil (0 kPa) showed a more rapid decline in nutrient independent germinability, viability and virulence, than to those exposed to −5 or −15 kPa. Sclerotia became dependent on nutrient for germination and lost viability and virulence within 30–40 days in soil at 25 or 30 °C, pH 8. However, more than 60% of sclerotia retained viability in soil at 15 °C regardless of pH, even after 50 days. Radish shoot growth was increased significantly by the sclerotia that had been exposed to soil at 0 kPa, or to soil at 25 or 30 °C and pH 8 for 50 days. In conclusion, carbon loss by sclerotia during incubation on soil at different pH levels, temperatures and water potentials was inversely correlated with sclerotial ability to infect radish seedlings. The relationship between carbon loss by sclerotia and radish shoot length was positive.  相似文献   

10.
This study was undertaken to investigate the feasibility of using Paecilomyces lilacinus NRRL 13 866, chitin, and cellulose amendments, in order to reduce survival and prevent germination of sclerotia from Aspergillus flavus NRRL 6556, NRRL 13 048, and A. parasiticus NRRL 13 005, NRRL 13 539 buried in sandy soil in Georgia and Illinois (April–October, 1990). The number of sclerotia that germinated sporogenically in moist chambers following burial in Illinois was twice that of sclerotia buried in Georgia and varied among the four sclerotium-producing Aspergillus spp. strains. Sclerotium viability, as measured by Aspergillus spp. colony formation on potato dextrose agar, was high (>84%) for all strains and treatments (e.g. amendment, location). Even so, A. parasiticus NRRL 13 539 sclerotia were apparently more susceptible to P. lilacinus colonization than sclerotia from other strains. Treatment with Paecilomyces sp. caused a small but significant reduction in germination among sclerotia buried in Georgia.  相似文献   

11.
A single injection of 0.2 ml diallyl disulphide (DADS) at 0.156% (v/v) into soil containing naturally-produced sclerotia of Sclerotium cepivorum and maintained in the laboratory at 15°C stimulated sclerotial germination and reduced sclerotial numbers by 67%; ungerminated sclerotia remained viable. Higher concentrations of DADS had no additional effect except that at 20% (v/v), germination was slightly inhibited. A similar reduction in sclerotial numbers was obtained when the mixture of soil and sclerotia was exposed to DADS vapour. Four, monthly applications of DADS at 0.2 ml 0.15% (v/v) per application did not give a further reduction.The effect of DADS was temperature dependant, with a reduction in sclerotial numbers of 65 and 9% at 15 and 5°C respectively.  相似文献   

12.
The effects of three Coniothyrium minitans isolates (Conio, IVT1 and Contans®), applied to soil as conidial suspensions or as maizemeal-perlite (MP) inocula (Conio), on apothecial production and infection of Sclerotinia sclerotiorum sclerotia were assessed in two soil pot bioassays and two novel box bioassays in the glasshouse at different times of the year. C. minitans isolate Conio applied as either MP or ground MP at full rate (106-107 cfu cm−3 soil) consistently decreased the carpogenic germination, recovery and viability of sclerotia and increased C. minitans infection of the sclerotia of S. sclerotiorum by in comparison with either MP or conidial suspension treatments applied at lower rates (103-104 cfu cm−3 soil). Additionally, when applied at the same rate, MP inoculum of C. minitans was consistently more effective at reducing carpogenic germination than a conidial suspension. The effect of MP and ground MP at full rate on carpogenic germination was expressed relatively early as those sclerotia recovered before apothecia appeared on the soil surface already had reduced numbers of apothecial initials. In general, there were few differences between the isolates of C. minitans applied as conidial suspensions. Box bioassays carried out at different times of the year indicated that temperature and soil moisture influenced both apothecial production and mycoparasitism. Inoculum concentration of C. minitans and time of application appear to be important factors in reducting apothecial production by S. sclerotiorum.  相似文献   

13.
The infection and survival of sclerotia of Sclerotinia minor and the production ofmacroconidia of the mycoparasite, Sporidesmium sclerotivorum, were studied in vitro when each fungus was added to soil at various initial inoculum densities. The rate at which S. sclerotivorum invaded host sclerotia and caused their decay varied with the amount of the mycoparasite added to soil. The results suggest that approximately 5 macroconidia of the mycoparasite g?1 of soil are needed to successfully infect sclerotia and bring about their decay, when soils are sampled and mixed every 2 weeks. The rate at which S. sclerotivorum infects sclerotia of S. minor and causes their decay is also dependent on the initial inoculum density of the host. Each infected sclerotium supports the production of about 15,000 new macroconidia in soil regardless of the initial inoculum density of the host. It is concluded that successful biological control by S. sclerotivorum is dependent on the soil population of both the host and the mycoparasite.  相似文献   

14.
Ten isolates of Trichoderma spp were examined for their ability to antagonize growth and to parasitize mycelium of Sclerotium rolfsii (Sr-1) on agar media, to inhibit germination of sclerotia of S. rolfsii on natural soil plates and to sporulate on the sclerotia, and to protect bean seedlings against the pathogen in the greenhouse. A high negative correlation (r = ?0.844) was observed between plant stand in the greenhouse and sclerotial germination on soil plates but not with antagonism on agar plates. Three isolates of T. harzianum (Th-7, Th-20, WT-6) and one of T. hamatum (TRI-4) were especially effective in reducing sclerotial germination and controlling disease in the greenhouse. Three isolates of Trichoderma spp (WT-6, TMP, and TRI-4), effective in reducing sclerotial germination of isolate Sr-1, also prevented sclerotial germination in four out of five additional S. rolfsii isolates studied.  相似文献   

15.
The development and survival of the mycoparasite Coniothyrium minitans associated with sclerotia of the plant pathogen Sclerotinia sclerotiorum was studied in pasteurised and non-sterile (untreated) soil. Using scanning electron microscopy, developing pycnidia were first seen within the sclerotial medulla at 7 days post-inoculation with the mycoparasite in pasteurised soil. However, by 14 days post-inoculation, pycnidia had developed fully in both pasteurised and non-pasteurised treatments, and conidial droplets were exuded onto the outer surface of the infected sclerotia. Thirty days post-inoculation, irrespective of soil treatment, the majority of the sclerotial medulla had been converted to pycnidia, with the sclerotial rind remaining largely intact. The pycnidia and dried intact droplets were still observed 6 months post-inoculation with C. minitans, although the conidia on the outer surface of the dried droplets had largely collapsed by this stage. Germinability studies at 10 months post-inoculation showed that approximately 13% of the conidia in dried droplets were still viable. This work shows the potential for infected sclerotia of S. sclerotiorum to provide a unique reservoir for the survival of C. minitans.  相似文献   

16.
The energy content of the mycoparasite Sporidesmium sclerotivorum mycelium was 18,389 J g?1 and 16,334 J g?1 for macroconidia on a dry weight basis. The energy content of Sclerotinia minor sclerotia, the host of the mycoparasite, was 16,485 J g?1. In liquid culture, the economic coefficient for the conversion of glucose to mycelium (mycelial dry wt ÷ glucose consumed × 100) was 51–60 whereas the mycelial energy coefficient, [mycelial energy (J) ÷ substrate energy (J) × 100] was 65–75. In soil, the conidial energy coefficient [conidial energy (J) ÷ substrate energy (J) × 100] for the conversion of host sclerotial energy to the macroconidia of the mycoparasite was 19.8, which was 2–9 times that for the conversion of glucose in liquid culture. The conidial energy coefficient when grown on a liquid medium on vermiculite was 23.0. S. sclerotivorum, as an obligate parasite of sclerotia in soil, was most efficient in the conversion of energy in a system where there was a high surface: energy ratio. In liquid culture S. sclerotivorum is more efficient than most other fungi.  相似文献   

17.
Direct observation of washed conidia of Cylindrocladium scoparium on non-sterile soils, air dried and rewetted immediately before deposition of conidia, indicated that peak germination (33–58%) occurred after 24 h incubation at 26°C. Peak germination on continually moist soils was lower (18–26%) than on rewetted soils. Lysis of germ tubes and germinating conidia on continually moist soils at 26°C was evident with 48 h. Conidia did not germinate on continually moist soils at 6°C and lysis did not become apparent until 168 h. Conidia germinated at a high level (93–99%) in axenic culture in the absence of exogenous C and N sources. The inhibition of conidial germination on soils may be attributed, in part, to the presence of soil volatiles. Germination of conidia placed on washed agar disks and exposed to volatiles from four soils ranged from 51 to 86% of the no-soil controls. Addition of carbon (13 ng C per conidium as glucose) and nitrogen (65 pg N ng?1 C as NH4C1) nullified the inhibitory effect of the soil volatiles. Germinability assayed on a selective medium at 26°C of conidia in artificially infested soils (approximately 104 conidia g?1 soil) decreased progressively during incubation at 26°C from 1 week to 4 months. No germinable conidia were recovered from artificially infested soils after 2 months incubation at 6°C. Conidia of C. floridanum and C. crotalariae responded similarly to C. scoparium in many assays.  相似文献   

18.
Six bacteria and one fungus isolated from sclerotia of Sclerotium cepivorum, the causal agent of white rot of onions, produced diffusible antibiotics antagonistic to growth of S. cepivorum on potato dextrose agar. Three of the bacterial isolates applied as seed treatments to onions grown in non-sterile muck soil in a controlled environment chamber reduced the proportion of infections by S. cepivorum. Antagonists were further evaluated as seed treatments for field control of white rot on two onion cultivars grown on muck soil containing high levels of natural inoculum. Four of the bacterial isolates provided significant season-long protection on the partially-resistant cultivar Festival, and the best of these also provided significant protection on the susceptible cultivar Autumn Spice. The fungal antagonist has been identified as Penicillium nigricans, and all bacterial isolates appear to be Bacillus subtilis. The levels of protection provided by some of these latter isolates were comparable to those provided by chemical treatments and represent practical potential for field control of white rot.  相似文献   

19.
The population and distribution of sclerotia of Rhizoctonia solani Kühn in two sugar beet field soils was determined at harvest by a sieving-flotation method. In rhizosphere soil (RS) and non-rhizosphere soil (NRS) from the most heavily infected roots of sugar beets, 1.43–2.5 and 0.83–1.0 sclerotia g?1 dry soil were detected, respectively. In the soil around healthy sugar beet, these values were 0.04–0.12 and 0.03–0.04 sclerotia g?1 dry soil. More sclerotia were always obtained from RS than from NRS. More than 80% of the sclerotia were in the upper 10 cm of soil and within 10 cm of diseased roots. Therefore, there is a non-uniform distribution of sclerotia of R. solani in soil.The sclerotial population in soil increased significantly with disease severity and a good correlation was obtained between the number of sclerotia and the disease severity on infected plants. Most of the sclerotia collected from the field soil ranged in size from 0.5 to 2.0 mm diameter.Viability of sclerotia increased as severity of crown rot increased and as the size of the sclerotia increased. Conversely, there was a progressive decrease in sclerotial germination with increasing depth in soil and increasing distance from the infected root.  相似文献   

20.
The rate at which dried soils are rewetted can affect the quantities and forms of nutrients in leachates. Both dried and moist replicated (n?=?3) samples of two contrasting grassland soil types (clayey vs brown earth) were irrigated during laboratory experiments with identical total amounts of water, but at different rates, ranging from 0 h, increasing by 30-min increments up to 4 h, and additionally a 24-h rewetting rate. Total P concentrations in leachates from dried samples of both soils generally decreased as rewetting rate increased, ranging from 2,923?±?589 μg P L?1 (0.5 h rewetting rate) to 731?±?46.0 μg P L?1 (24 h, clayey soil) and 1,588?±?45.1 μg P L?1 (0.5 h) to 439?±?25.5 μg P L?1 (24 h brown earth). Similar patterns in concentrations occurred for molybdate reactive P (MRP), although concentrations were generally an order of magnitude lower, indicating that the majority of the leached P was probably organic. The moist brown earth leached relatively high concentrations of MRP (maximum 232?±?10.6 μg P L?1, 0.5 h), unlike the moist clayey soil (maximum 20.4?±?10.0 μg P L?1, 0 h). The total oxidised N concentrations in leachates were less affected by rewetting rate, although longer rewetting rates resulted in decreased concentrations in leachates from the dried samples of both soils. The difference in responses to rewetting rates of the two soils is probably due to differences in the fate of the microbial biomass and adsorption properties in the soils. Results show that soil moisture could be an important factor in regulating nutrient losses and availability, especially under changing patterns of rainfall predicted by future climate change scenarios.  相似文献   

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