Soil surfactants influence fungicide movement in United States Golf Association putting green soil.

The management of root and crown diseases of turfgrasses is challenging. To manage these diseases, golf course superintendents and other turfgrass managers often spray fungicides at a high carrier volume and irrigate after application to move fungicides into the root zone. Furthermore, previous research has demonstrated that soil surfactants can increase fungicide movement and distribution in soil. Two laboratory experiments were conducted using lysimeters, which were coated with sand on their inner walls to prevent preferential flow and contained 90/10% sand/peat moss (v/v), to determine the effects of soil surfactants on movement of selected fungicides in soil. The soil surface in the first experiment was treated three times at 2-wk intervals with one of three soil surfactants: Aquifer (propoxylated polyethylene glycols), Fleet (polyoxyalkylene polymers), and Revolution (modified alkylated polyol). The soil in the second experiment was treated with only Revolution four times at 2- to 3-wk intervals. Immediately after the final surfactant application, soil columns were treated with 14 C-labeled fungicide. 14 C-Myclobutanil was applied in the first experiment, and 14 C-azoxystrobin and 14 C-propiconazole were applied in the second experiment. In the first experiment, 14 percent units more of the recovered 14 C-myclobutanil was detected in the 5- to 7.6-cm sampling depth, and >4 percent units more was detected in the 7.6- to 10.2-cm depth after soil surfactant application compared with the fungicide-alone treatment. Each soil surfactant also yielded >28% more leachate than the nontreated control. In the second experiment, the total recovered 14 C-azoxystrobin and 14 C-propiconazole in the 7.6- to 10.2-cm depth increased by 2.8 and 1.9 percent units, respectively, compared with soil treated with fungicide alone. These data indicate that soil surfactant inclusion may increase fungicide distribution in soil, which may enhance the efficacy of fungicides in suppressing root and crown diseases.

Enhanced Overwintering Survival of Stevia by QoI Fungicides Used for Management of Sclerotium rolfsii.

Stevia (Stevia rebaudiana) is a herbaceous perennial under evaluation as a new crop in the southeastern United States. Stem rot caused by Sclerotium rolfsii is common in stevia plantings in North Carolina, with symptoms including wilting, root and stem necrosis, and plant death. Fungicide efficacy trials for management of S. rolfsii were conducted over 2 years. Fungicides evaluated included azoxystrobin, flutolanil, and tebuconazole applied at three timings. Azoxystrobin applied to transplants 1 week prior to planting had the lowest area under the disease progress curve values across all trials. Fungicide plots were also used to evaluate overwintering of stevia. End-of-season stand counts were compared with spring emergence counts to quantify overwintering survival. In spring 2015, plots treated with azoxystrobin in 2014 had greater overwintering survival (78%) than other fungicide treatments (38%) and the control (38%). Similar results were obtained at two locations in spring 2016 in plots treated with azoxystrobin or pyraclostrobin in 2015. Successful overwintering of stevia directly impacts the profitability of second- and third-year harvests and enhances the likelihood of long-term establishment of stevia as a viable crop. Future studies will be directed at elucidating the mechanism of the enhanced overwintering survival of plants treated with quinone outside inhibitor fungicides.

Variability for Resistance to Phytophthora nicotianae Within a Collection of Nicotiana rustica Accessions.

Black shank, caused by Phytophthora nicotianae, is one of the most important diseases affecting tobacco (Nicotiana tabacum) production worldwide. Many current tobacco cultivars possess immunity to race 0 of this pathogen conferred by introgressed dominant genetic factors. Novel alleles conditioning resistance to alternative races are desired. The objective of this research was to evaluate variability for black shank resistance within a collection of N. rustica germplasm using both soilborne disease nurseries and controlled race-specific (race 0 and race 1) inoculations. Nearly all of the 86 accessions studied exhibited very high resistance to race 0, and many displayed levels of race 1 resistance greater than that exhibited by the resistant flue-cured tobacco check, 'K 346'. Materials found to be highly resistant to race 0 and race 1 in growth-chamber experiments also had the best survivability in field disease nurseries. N. rustica accessions TR 6, TR 12, TR 16, TR 21, TR 20, TR 48, TR 54, TR 57, and TR 69 could be sources of novel alleles with large effects on black shank resistance, and could have value for burley and flue-cured tobacco breeding.

Occurrence of Race 3 of Phytophthora nicotianae in North Carolina, the Causal Agent of Black Shank of Tobacco.

Black shank, caused by the oomycete Phytophthora nicotianae, causes significant annual yield losses in tobacco. Race 3 of P. nicotianae is reported here for the first time from North Carolina. It was identified from a North Carolina tobacco field with a history of tobacco varieties with Phl gene resistance and numerous field sites with no known deployment of varieties with the Phl gene. Race 3 was originally described from cigar-wrapper tobacco in Connecticut in the 1970s, but has not been reported in any other location since. Race 3 was defined as overcoming the Phl gene from Nicotiana longiflora but not the Php gene from N. plumbaginifolia. Stem and root inoculations were conducted on a set of host differentials to determine the virulence of North Carolina isolates. Stem inoculation was unable to distinguish between races 0 and 3 of P. nicotianae and is not a reliable method of identifying these virulence types. Race 1 gave a unique phenotype using stem inoculation. Root inoculation was the only reliable means of distinguishing between races 0 and 3. This is the first report of race 3 in North Carolina and the first report of damage to seedlings from root inoculations and to plants containing the Phl gene in naturally infested soil.

An Assessment of the Genetic Diversity in a Field Population of Phytophthora nicotianae with a Changing Race Structure.

One hundred fifty-three isolates of Phytophthora nicotianae that were collected over a 4-year period from a single field were subjected to amplified fragment length polymorphism (AFLP) analysis to investigate the effect of different types of resistance in tobacco (Nicotiana tabacum) on genetic diversity in the pathogen population. No race 1 isolates were detected in the field prior to initiating the study, but the race was present in multiple plots by the end of the 4-year period. There were 102 race 0 isolates and 51 race 1 isolates characterized. Seventy-six of the 153 isolates had a unique AFLP profile, whereas the remaining 77 isolates were represented by 27 AFLP profiles shared by at least two isolates. Isolates of both races were found in both the unique and shared AFLP profile groups. Twenty-three of the AFLP profiles were detected in multiple years, indicating a clonal component to the pathogen population. Race 1 isolates that were detected over multiple years were always obtained from the same plot. No race 1 profile was found in more than one plot, confirming the hypothesis that the multiple occurrences of the race throughout the field were the result of independent events and not pathogen spread. Three identical race 0 AFLP profiles occurred in noncontiguous plots, and in each case, the plots contained the same partially resistant variety. Cluster analysis provided a high level of bootstrap support for 41 isolates in 19 clusters that grouped primarily by race and rotation treatment. Estimates of genetic diversity ranged from 0.365 to 0.831 and varied depending on tobacco cultivar planted and race. When averaged over all treatments, diversity in race 1 isolates was lower than in race 0 isolates at the end of each season. Deployment of single-gene resistance initially decreased genetic diversity of the population, but the diversity increased each year, indicating the pathogen was adapting to the host genotypes deployed in the field.

Evaluation of Tobacco Germplasm for Seedling Resistance to Stem Rot and Target Spot Caused by Thanatephorus cucumeris.

Stem rot and target spot of tobacco, caused by Rhizoctonia solani and its teleomorph Thanatephorus cucumeris, respectively, can cause serious problems in production of tobacco (Nicotiana tabacum) seedlings. Previous screens for genetic resistance in tobacco have been limited. The objective of this study was to evaluate 97 genotypes composing several classes of tobacco and related Nicotiana spp. for seedling resistance to stem rot and target spot. Significant differences in disease incidence initially were observed among the genotypes for both stem rot and target spot; however, resistance to target spot was not observed when disease pressure was high. Partial resistance to stem rot was observed in several genotypes in repeated tests. These accessions may be useful as a source of resistance to R. solani in future breeding efforts.

Differential Sensitivity of Phytophthora parasitica var. nicotianae and Thielaviopsis basicola to Monomeric Aluminum Species.

ABSTRACT Aluminum (Al) is toxic to many plant pathogens, including Thielaviopsis basicola and Phytophthora parasitica var. nicotianae. Because fungi-toxicity of Al has been described in soils over a wide pH range, multiple species of Al may be responsible for pathogen suppression. The goals of this work were to determine the sensitivity of T. basicola and P. para-sitica var. nicotianae to Al over a range of pH values, quantify the toxicity of monomeric Al species to production of sporangia of P. parasitica var. nicotianae and chlamydospores of T. basicola, and detect the accumulation of Al in pathogen structures. A complete factorial treatment design was used with Al levels ranging from 0 to 100 muM and pH levels ranging from 4 to 6 in a minimal salts medium. The chemistry of test solutions was modeled using GEOCHEM-PC. Colonies were grown in 5% carrot broth, and after 1 or 2 days, the nutrient solution was removed, colonies were rinsed with water, and Al test solutions were added to each of four replicate plates. After 2 days, propagules were counted and colonies were stained with the Al-specific, fluorescent stain lumogallion. The oomycete P. parasitica var. nicotianae was sensitive to multiple monomeric Al species, whereas sensitivity of T. basicola to Al was pH-dependent, suggesting that only Al(3+) is responsible for suppression of this fungal pathogen. Chlamydospore production by T. basicola was inhibited at pH values <5.0 and Al levels >20 muM, whereas sporangia production by P. parasitica was inhibited at Al levels as low as 2 muM across all pH values tested. The lumogallion stain was an effective technique for detection of Al in fungal tissues. Aluminum accumulated in sporangia and zoospores of P. parasitica var. nicotianae and in nonmelanized chlamy-dospores of T. basicola, but not in cell walls of either organism. The differential sensitivity of the two organisms may indicate that true fungi respond differently to Al than members of the oomycota, which are more closely related to plants.

Fitness of Races 0 and 1 of Phytophthora parasitica var. nicotianae.

Deployment of tobacco (Nicotiana tabacum) varieties with complete resistance to race 0 of Phytophthora parasitica var. nicotianae has led to a rapid increase in the field populations of race 1 in North Carolina. In a field study, population levels of race 1 decreased relative to race 0 when cultivars with partial resistance to both races were planted, suggesting that race 1 isolates were less fit than race 0 isolates. Experiments were conducted to quantify differences in aggressiveness and survivability of the two races. Tobacco varieties with low, moderate, or high levels of partial resistance were inoculated with 60 pathogen isolates, and symptom development was monitored for 3 weeks. Race 0 isolates were more aggressive than race 1 isolates on cultivars with moderate or high levels of partial resistance; incubation periods were shorter and root rot severity was greater with race 0 isolates. Isolates of race 1, however, caused greater stunting of plants with moderate and high levels of partial resistance than race 0 isolates. Field microplots were infested with either a single race or an equal mixture of each race. Soil samples were collected at the end of two growing seasons and again the following spring. Pathogen populations declined from 40 to 80% during winter months, but population declines for race 0 were lower than for race 1 in each treatment over each winter. Race shifts from race 1 to race 0 that were observed in the presence of cultivars with partial resistance appear to be primarily the result of differences in aggressiveness of the races, with a possible minor effect of enhanced overwintering survival of race 0 compared with race 1.

Managing the Race Structure of Phytophthora parasitica var. nicotianae with Cultivar Rotation.

Deployment of tobacco cultivars with single-gene, complete resistance to race 0 of the tobacco black shank pathogen, Phytophthora parasitica var. nicotianae, has resulted in a rapid increase in the occurrence of race 1 of the pathogen in North Carolina. Cultivar-rotation studies were conducted in three fields to assess how different levels and types of resistance affected the race structure and population dynamics of the pathogen when deployed in fields initially containing single or mixed races of the pathogen. In a field with both races present, a high level of partial resistance in cv. K 346 was most effective in reducing disease and decreasing the proportion of race 1 in the pathogen population. The deployment of complete resistance in cv. NC 71 resulted in intermediate levels of disease control and race 1 became the predominate race. The cv. K 326, with a low level of partial resistance, had the highest levels of disease, and race 0 was the dominant race recovered. In a field where no race 1 was detected initially, disease incidence was high with the use of partial resistance. Complete resistance was very effective in suppressing disease, but race 1 was recovered after only one growing season. By the end of the third growing season, race 1 was recovered from most treatments where single-gene resistance was deployed. A high level of partial resistance was most effective in suppressing disease in a field where race 1 initially was the predominant race. A rotation between cultivars with single-gene resistance and cultivars with a high level of partial resistance should provide the most effective approach to black shank management. This rotation will reduce disease incidence and minimize race shifts in the pathogen and, over time, should prolong the usefulness of the Ph gene for black shank control in commercial production of tobacco.

Abiotic and Biological Suppression of Phytophthora parasitica in a Horticultural Medium Containing Composted Swine Waste.

ABSTRACT Horticultural potting media have been amended with compost to enhance biological suppression and with Al(2)(SO(4))(3) to enhance abiotic suppression of plant pathogens, but these factors have not been simultaneously incorporated into the same medium. In this study, the efficacy of aluminum (Al)-amended potting medium containing 20% composted swine waste (CSW) was assessed for control of Phytophthora parasitica (syn. P. nicotianae), a soilborne pathogen causing damping-off of many horticultural bedding plants. Steamed and unsteamed media were amended with no Al or Al at 0.0079 g of Al g(-1) of medium with an Al(2)(SO(4))(3) solution at either pH 4 or pH 6. Infested leaf disks were buried for 2-day durations beginning 0, 6, 13, and 21 days after Al amendment. The number of sporangia produced on infested leaf disks was assessed. A similar experiment was conducted to determine the effect of steaming and Al amendments on pathogen populations. Medium treated with the pH 4 solution consistently reduced sporangia production between 38 and 65% on day 0, but no Al effect was noted at subsequent time points. The pH 6 amendment did not consistently affect sporangia production. Exchangeable Al levels decreased over time, and abiotic suppression was only observed at >2 muM Al g(-1) of medium. Pathogen populations were occasionally affected by steaming and Al. Sporangia production in unsteamed medium was reduced by 50% on leaf disks buried on days 6, 13, and 21, but not on day 0. Al amendment of a 20% CSW potting medium enhanced suppression of P. parasitica and abiotic suppression occurred before biological suppression developed.

Origin of the Black Shank Resistance Gene, Ph, in Tobacco Cultivar Coker 371-Gold.

Flue-cured tobacco (Nicotiana tabacum) cultivar Coker 371-Gold (C 371-G) possesses a dominant gene, Ph, that confers high resistance to black shank disease, caused by race 0 of the soil-borne pathogen Phytophthora parasitica var. nicotianae. The origin of this gene is unknown. Breeding lines homozygous for the Ph gene were hybridized with NC 1071 and L8, flue-cured and burley genotypes known to possess qualitative resistance genes from Nicotiana plumbaginifolia and N. longiflora, respectively. The F1 hybrids were out-crossed to susceptible testers and the progenies evaluated in field black shank nurseries and in greenhouse disease tests with P. parasitica var. nicotianae race 0. Results showed that Ph was allelic to Php from N. plumbaginifolia in NC 1071. Testcross populations of hybrids between burley lines homozygous for Ph and L8, possessing Phl from N. longiflora, showed that Ph and Phl integrated into the same tobacco chromosome during interspecific transfer. Nevertheless, the two loci were estimated to be 3 cM apart. Random amplified polymorphic DNA (RAPD) analyses of the testcross progenies confirmed that recombination between the two loci was occurring. Forty-eight RAPD markers linked to Ph in doubled haploid lines were used in cluster analyses with multiple accessions of N. longiflora and N. plumbaginifolia, breeding lines L8, NC 1071, and DH92-2770-40, and cultivars K 326, Hicks, and C 371-G. A cladogram or region tree confirmed the data obtained from field and greenhouse trials, that Ph, transferred from C 371-G to DH92-2770-40, and Php in NC 1071 were allelic and originated from N. plumbaginifolia.

Nonphytotoxic Aluminum-Peat Complexes Suppress Phytophthora parasitica.

ABSTRACT Amendment of peat-based potting media with Al(2)(SO(4))(3) suppresses damping-off of Vinca (Catharanthus roseus) caused by Phytophthora parasitica. The species of aluminum (Al) responsible for disease suppression have not been identified. The objective of this study was to determine the effects of amount and pH of Al(2)(SO(4))(3) amendment solutions on survival of P. parasitica. In separate experiments, peat was amended with Al(2)(SO(4))(3) solutions adjusted to pH 4 or 6 at either 0.0158 or 0.0079 g of Al per gram of peat. Amended peat was placed in Büchner funnels maintained at -2.5 kPa matric potential. Peat was infested with P. parasitica by placing zero, two, or five colonized Vinca leaf disks in each funnel, and 15 Vinca seeds were placed in each funnel. After 24 h, the matric potential was brought to 0 kPa to induce zoospore release and returned to -2.5 kPa after 24 h. Pathogen populations and stand counts were assessed after 2-week incubation. Al amendment solutions at both pH 4 and 6 reduced pathogen populations at 0.0158 g of Al per gram of peat. Solutions at pH 4 reduced pathogen populations by more than 90% at both inoculum levels; amendment solutions at pH 6 reduced populations by 95% at the low inoculum level and 65% at the high inoculum level. The prevalence of Al(OH)(2)(+) in peat amended with Al(2)(SO(4))(3) solution at pH 6 suggests that ions other than Al(3+) may be responsible for pathogen suppression. Based on the difference in chemical conditions of Al-amended peat and suppressive mineral soils, the mechanism of Al-mediated suppression of plant pathogens is speculated to be different in the two systems. Peat containing Al-peat complexes was chemically suppressive to P. parasitica and may confer Al-mediated suppression of plant pathogens with a nonphytotoxic form of Al.

Factors that Affect Development of Collar Rot on Tobacco Seedlings Grown in Greenhouses.

Collar rot, caused by Sclerotinia sclerotiorum, is an important disease of tobacco transplants produced under greenhouse conditions. Factors that affect the development of the disease were studied, including age of seedlings, presence of an external source of nutrients (leaf extract), clipping (leaf removal) practices, exposure to low temperature, and leaf injury caused by heat and a chemical. Flue-cured tobacco seedlings, cultivar K-326, were grown in polystyrene cell trays floating on a nutrient solution. Trays were maintained in a phytotron growth chamber with a 28/18°C day/night temperature regime. Seedlings were inoculated with ascospores of S. sclerotiorum at the desired stage of growth by placing mature apothecia in the growth chamber and inducing ascospore release and deposition. Disease incidence was determined by examining seedlings for the presence of stem lesions over the next 15 to 21days. Seedlings between 35 and 53 days old were more susceptible to collar rot than younger or older seedlings. Inoculum efficiency was highest and disease was most severe when an external source of nutrients was present on leaf surfaces. Clipping of leaf tips did not increase disease, but if the leaf pieces created by clipping were left on seedlings, collar rot development was enhanced compared with treatments where debris was removed. Heat and chemical injuries that resulted in necrotic tissue provided highly susceptible infection courts for ascospores of S. sclerotiorum, but exposure to low temperature, which caused no visible injury, did not enhance infection. Adoption of cultural practices that minimize accumulation of leaf debris and eliminate factors that cause necrotic injury on leaves should greatly reduce the severity of collar rot of tobacco seedlings.

Evaluation of Wounds as a Factor to Infection of Cabbage by Ascospores of Sclerotinia sclerotiorum.

A semi-selective medium was used to examine the aerobiology of ascospores of Sclerotinia sclerotiorum in five commercial cabbage fields in eastern North Carolina. Ascospores were present in all five fields from 26 September to 30 November. However, numbers of ascospores varied greatly depending on location, sampling date, and time. In general, peak ascospore deposition occurred between 11:00 A.M. and 1:00 P.M., with the number of colonies recovered ranging from 3 to 55/dish (9 cm in diameter). Peak ascospore numbers at all locations were found from mid- to late October, but a second, smaller peak was also evident at each location in late November. Information obtained was employed to evaluate the role of wounding in infection of cabbage by ascospores of S. sclerotiorum in controlled environmental chambers. A method for production and release of ascospores of S. sclerotiorum was employed in controlled-environment chambers for the inoculation of cabbage plants with one of three representative foliar wounds: a bruise, a cut, or a non-lethal freeze. Wounding treatments were applied to 7-week-old cabbage plants, misting was added to maintain continuous leaf wetness, and ascospores were released from apothecia twice daily for four consecutive days. Spore trapping with a semi-selective medium indicated that inoculum was evenly distributed within the chambers and deposition was similar to levels recorded in the field. At 31 days after inoculation, disease incidence ranged from 0% on the control to 96% on the freeze treatments. Freeze-treated plants showed the highest disease severity throughout the entire incubation period. Mean area under the disease progress curve of severity values were 0, 0.2, 34 and 60 for the control, cut, bruise, and freeze treatments, respectively. Results indicate that freeze and bruise injuries are important factors associated with infection of cabbage by S. sclerotiorum.

Identification and Quantification of Ascospores as the Primary Inoculum for Collar Rot of Greenhouse-Produced Tobacco Seedlings.

Collar rot, caused by Sclerotinia sclerotiorum, is a severe disease of tobacco seedlings grown in greenhouses. A semiselective medium was adapted and used to detect the presence and quantity of ascospores in commercial greenhouses. Petri dishes of the semiselective medium were placed inside and outside of greenhouses in four counties during the transplant production period in 1995 and 1996. Ascospores were present throughout the production period each year (February to April) and were confirmed to be the primary inoculum for the disease. Significant differences were observed in the number of ascospores trapped within and between counties. Peak numbers of ascospores were trapped between 10 and 12 a.m., and higher numbers of ascospores were trapped outside than inside houses. In general, distribution of ascospores inside houses was uniform unless a high concentration of apothecia was present very close to one section of the greenhouse. The semiselective medium and trapping technique used in this study may allow development of a forecasting system for collar rot of tobacco based on the presence and level of pathogen inoculum.

Initial Cellular Interactions Between Thielaviopsis basicola and Tobacco Root Hairs.

ABSTRACT Cellular events that occur during the initial interactions between Thielaviopsis basicola and root hairs of tobacco (Nicotiana tabacum) were examined microscopically. Time-course documentation of the infection process indicated a dynamic interaction between T. basicola and the living host cell. Upon root hair contact and recognition, the vegetative apex of T. basicola rapidly differentiated to form infection structures, and the host cell responded cytologically. Penetration was achieved by threadlike hyphae that subsequently developed distal swellings, and intracellular hyphae of sickle-shaped morphology advanced from the distal swelling and colonized the cell. Streaming of the host cytoplasm became aggregated near the infection site prior to penetration and accumulated around the infecting hyphae as long as the host cell was viable. Substantial callose deposition, in the form of a bell-shaped collar around infection structures, resulted from the cytological activity at the infection site. Penetration of dead root hairs was common, but did not lead to the development of infection structures or to a sustained association with the host tissue; T. basicola exited dead root hairs and resumed vegetative growth. The establishment of the parasitic relationship by T. basicola was characteristic of hemibiotrophic fungi in that, initially, biotrophic infection led to tissue colonization, and host cell survival was limited under parasitism.

Inheritance of Resistance to Race 0 of Phytophthora parasitica var. nicotianae from the Flue-Cured Tobacco Cultivar Coker 371-Gold.

Black shank, caused by Phytophthora parasitica var. nicotianae, is a widespread and severe disease of tobacco throughout the southeastern United States. Partial resistance derived from the cigar tobacco cultivar Florida 301 has been the primary means of reducing losses to the disease for many years. The recently released tobacco cultivar, Coker 371-Gold (C 371-G), was found to provide an additional source of resistance to P. parasitica var. nicotianae. Although the resistance in C 371-G is being used widely by breeders, the origin and inheritance of this resistance mechanism was unknown. Two populations of doubled haploid lines derived from C 371-G were used to determine that C 371-G possesses a single, dominant gene designated Ph, which confers a very high level of resistance to race 0 of P. parasitica var. nicotianae. A greenhouse inoculation procedure was developed that provided an efficient means of screening for the presence of this resistance gene prior to selection in the field, and confirmed that Ph provides complete resistance to race 0 but no resistance to race 1 of P. parasitica var. nicotianae. Because Florida 301 resistance is effective against both races of the pathogen that occur in the major tobacco growing areas of the United States, combination of these two sources of resistance should provide enhanced protection of new tobacco cultivars to P. parasitica var. nicotianae.

Sources of Inoculum and Management for Rhizoctonia solani Damping-off on Tobacco Transplants under Greenhouse Conditions.

Damping-off and target spot are important diseases of tobacco transplants produced under greenhouse conditions. Identification of sources of inoculum for these diseases caused by Rhizoctonia solani is an important first step in disease management. Control strategies based on sanitation and the eradication of primary inoculum were studied. Potting mix and Styrofoam trays used in transplant production were assayed to determine if they were sources of primary inoculum. Eleven sources of potting mix were sampled over a 2-year period. None of the mixes contained viable inoculum of R. solani. R. solani was isolated from previously used trays after 1 year of storage by removing and plating pieces of Styrofoam from individual tray cells on alkaline water agar (AWA). Sclerotia and melanized hyphae of R. solani were observed in the cracks present in the cells of the trays. Dry heat (70 to 80°C for 2 h) and chemical (sodium hypochlorite and sodium chloride) treatments reduced the levels of inoculum on trays up to 45% compared to controls, but only methyl bromide and steam treatments (80°C for 0.5 to 2.0 h) eradicated inoculum of R. solani from trays. Elimination of primary inoculum from previously used trays effectively controlled target spot and stem rot diseases caused by R. solani.

Reassessment of the Role of Saprophytic Activity in the Ecology of Thielaviopsis basicola.

ABSTRACT The ability of Thielaviopsis basicola to survive saprophytically in soil was investigated using root tissue from susceptible hosts as organic substrates. Inoculum densities were lower in soils amended with root tissue than in nonamended controls after 2 and 4 weeks of incubation. The greatest decrease occurred in soils containing the highest concentration of root tissue or in soils in which root tissue included the soluble components of the living root. Reproduction by T. basicola also was examined in axenic media containing either killed root pieces or various carbohydrates as the sole carbohydrate source. T. basicola utilized killed root tissue as a carbohydrate source in axenic media, particularly in cultures in which root tissue included the soluble components. Enzymatic activities of T. basicola, however, did not result in maceration of the root tissue. T. basicola utilized sucrose and cellobiose, but did not utilize structural carbohydrates such as cellulose, hemicellulose, or pectin. Based on the absence of significant saprophytic ability, T. basicola should be classified ecologically as an obligate parasite.