Abstract:Rhizoctonia web blight is an annual problem on container-grown azalea (Rhododendron spp.) in the southern and eastern United States but little is documented about the distribution or persistence of Rhizoctonia spp. in container-grown azalea. Sixty web-blight-damaged azalea plants (‘Gumpo White’) were collected in August 2005 and 2006 and arranged in a completely randomized design on an outdoor irrigation pad. A nylon mesh bag containing 30 necrotic leaves collected from web-blight-damaged ‘Gumpo White’ azalea … Show more
Moisture variables have not been a consistent predictor of Rhizoctonia web blight development on container‐grown azalea. A vapour pressure deficit <2.5 hPa was the only moisture variable attributed to slow web blight development in one study, yet in another study, frequent rainfall provided a moderately successful decision criterion for applying fungicide. To characterize web blight development in response to leaf wetness, plants were inoculated with two isolates of binucleate Rhizoctonia AG‐U and maintained in a glasshouse in open‐topped, clear plastic chambers with 0‐, 4‐, 8‐, 12‐, 16‐ and 20‐h daily cycles of 20–30 s mist at 30‐min intervals under day and night temperatures of 29 and 22°C, respectively. Leaf wetness duration closely matched misting cycle duration. Disease incidence was measured per chamber as a mean of the number of blighted leaves per total leaves per stem. A mixed model procedure was used to compare area under the disease progress curves (AUDPC) over 4–6 weeks in experiments performed in 2008 to 2010. Isolate response to mist cycle durations was not different (P = 0.4283) in 2008, but was different in 2009 (P = 0.0010) and 2010 (P < 0.0001) due to one isolate becoming less aggressive over time. AUDPC was consistently higher on azaleas under 16‐ and 20‐h mist cycles, which formed a higher disease group not significantly different from each other. AUDPC under 0‐, 4‐, and 8‐h mist cycles mostly formed a lower disease group, while ranking for a 12‐h mist cycle varied across experiments from the higher, intermediate, or lower AUDPC groups. Current data demonstrate an empirical relationship between long daily leaf wetness durations and development of severe web blight symptoms within a temperature range considered favourable for Rhizoctonia web blight development. Additional studies would be required to model Rhizoctonia web blight development under natural temperature fluctuations.
Moisture variables have not been a consistent predictor of Rhizoctonia web blight development on container‐grown azalea. A vapour pressure deficit <2.5 hPa was the only moisture variable attributed to slow web blight development in one study, yet in another study, frequent rainfall provided a moderately successful decision criterion for applying fungicide. To characterize web blight development in response to leaf wetness, plants were inoculated with two isolates of binucleate Rhizoctonia AG‐U and maintained in a glasshouse in open‐topped, clear plastic chambers with 0‐, 4‐, 8‐, 12‐, 16‐ and 20‐h daily cycles of 20–30 s mist at 30‐min intervals under day and night temperatures of 29 and 22°C, respectively. Leaf wetness duration closely matched misting cycle duration. Disease incidence was measured per chamber as a mean of the number of blighted leaves per total leaves per stem. A mixed model procedure was used to compare area under the disease progress curves (AUDPC) over 4–6 weeks in experiments performed in 2008 to 2010. Isolate response to mist cycle durations was not different (P = 0.4283) in 2008, but was different in 2009 (P = 0.0010) and 2010 (P < 0.0001) due to one isolate becoming less aggressive over time. AUDPC was consistently higher on azaleas under 16‐ and 20‐h mist cycles, which formed a higher disease group not significantly different from each other. AUDPC under 0‐, 4‐, and 8‐h mist cycles mostly formed a lower disease group, while ranking for a 12‐h mist cycle varied across experiments from the higher, intermediate, or lower AUDPC groups. Current data demonstrate an empirical relationship between long daily leaf wetness durations and development of severe web blight symptoms within a temperature range considered favourable for Rhizoctonia web blight development. Additional studies would be required to model Rhizoctonia web blight development under natural temperature fluctuations.
“…Temporal studies on Rhizoctonia web blight on azalea in south ern M ississippi have reported several different weather conditions that are conducive for disease development (4)(5)(6)(7)(8). Rhizoctonia web blight development on azalea was initially correlated with air tem peratures between 25 and 30°C for 6 to 8 h per day, relative humid ity >95% for >8 h per day, and/or leaf wetness for >6 h per day (7).…”
mentioning
confidence: 99%
“…The rate and degree o f web blight development differed between wet, moderate, and dry years, and weather variables o f tem pera ture, rainfall, and duration o f leaf wetness do influence disease development and control (4)(5)(6)(7)(8). Rhizoctonia web blight on azalea behaves like a polycyclic disease (7,8,14).…”
mentioning
confidence: 99%
“…M ycelium serves as primary and secondary inoculum. In the southeastern United States, mycelium persists in the azalea canopy 12 months o f the year (6). The mycelium density declines by early spring and builds up again by summer, probably in a cyclic growth pattern that corre lates with episodic leaf blight development.…”
mentioning
confidence: 99%
“…The mycelium density declines by early spring and builds up again by summer, probably in a cyclic growth pattern that corre lates with episodic leaf blight development. Binucleate Rhizoctonia fungi that cause web blight produce psuedosclerotia, but it is un clear if it plays a distinct role as primary inoculum (6). The pres ence of basidiospores has not yet been determined.…”
Copes, W. E. 2015. Weather-based forecasting of Rhizoctonia web blight development on container-grown azalea. Plant Dis. 99:100-105.The most reliable approach for timing fungicides to control Rhi zoctonia web blight on container-grown azalea has been a fixed calen dar date. The purpose of this study was to model periods when a pre ventive control could be applied in advance of significant increases in leaf blight intensity (LBI) in response to a daily accumulated risk value indicating conducive conditions of temperature (18 or more hours between 20 and 30°C when maximum temperature is less than 35°C), leaf wetness (16 or more hours), and/or rainfall (greater than 6.7 mm above the maximum daily irrigation). Analysis used weather measure ments taken every 30 minutes from 11 site-year datasets from 2006 to 2011, and weekly or biweekly LBI assessments. Six developmental site-year datasets were analyzed using receiver operating characteristic (ROC) curve procedures to evaluate models. Only a single model pre dicted true positives and negatives significantly greater than a 50:50 probability. Subsequently, five site-year validation datasets were evalu ated. Similar results were obtained from both the developmental and validation datasets, which produced ROC areas of 0.7715 (P = 0.0120) and 0.8393 (P = 0.0034), respectively. The practical application of weather-based forecasting for management of web blight in nurseries is discussed.
The medicinal effects and techniques for cultivating Anoectochilus formosanus are well-documented, but little is known about the mycorrhizal fungi associated with A. formosanus. Rhizoctonia (Thanatephorus) anastomosis group 6 (AG-6) was the most common species isolated from fungal pelotons in native A. formosanus and represented 67 % of the sample. Rhizoctonia (Ceratobasidium) AG-G, P, and R were also isolated and represent the first occurrence in the Orchidaceae. Isolates of AG-6, AG-R, and AG-P in clade I increased seed germination 44–91 % and promoted protocorm growth from phases III to VI compared to asymbiotic treatments and isolates of AG-G in clade II and Tulasnella species in clade III. All isolates in clades I to III formed fungal pelotons in tissue-cultured seedlings of A. formosanus, which exhibited significantly greater growth than nonmycorrhizal seedlings. An analysis of the relative effect of treatment () showed that the low level of colonization () by isolates in clade I resulted in a significant increase in seedling growth compared to isolates in clades II (0.63–0.82) and III (0.63–0.75). There was also a negative correlation (r = −0.8801) with fresh plant weight and fungal colonization. Our results suggest that isolates in clade I may represent an important group associated with native populations of A. formosanus and can vary in their ability to establish a symbiotic association with A. formosanus. The results presented here are potentially useful for advancing research on the medicinal properties, production, and conservation of A. formosanus in diverse ecosystems.Electronic supplementary materialThe online version of this article (doi:10.1007/s00572-014-0616-1) contains supplementary material, which is available to authorized users.
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