scholarly journals Southern Blight of Areca Palm (Chrysalidocarpus lutescens) Caused by Sclerotium rolfsii in California

Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 1012-1012
Author(s):  
S. T. Koike

Areca palm (Chrysalidocarpus lutescens) is a popular ornamental palm that can be grown outdoors in mild climates and is commonly used as an indoor ornamental plant. During 2005, commercial palm producers lost significant numbers of areca palm seedlings grown in transplant trays to a crown rot disease. Initial symptoms consisted of a light brown discoloration of stems near the soil line. As disease progressed, the brown discoloration extended up the stem and down into the crown, foliage became gray green, and the entire plant then dried up and died. Extensive, white, cottony mycelium and numerous sclerotia developed externally on the lower stem, crown, attached palm seed, and surrounding peat moss medium. Mycelial growth was so extensive that the fungus often grew from one transplant tray cell, bridged across the plastic cell border, and into an adjacent transplant cell. Tan, spherical sclerotia measured approximately 1 mm in diameter. Isolations from diseased plants resulted in the recovery of the same white fungus that produced sclerotia. On the basis of sclerotia morphology and the presence of clamp connections at hyphal septa, the fungus was identified as Sclerotium rolfsii. Pathogenicity was tested by growing isolates on potato dextrose agar, drying the resulting sclerotia for 48 h, and then depositing 8 to 10 sclerotia at the base of healthy areca palm seedlings. Five isolates were tested using 40 plants per isolate. Non-inoculated controls were also included. All plants were incubated in a greenhouse at 22 to 25°C. After 2 weeks, inoculated plants began to show brown necrosis at the base of the stems; by the third week, plants began to dry up, and mycelium and sclerotia developed on the crowns. S. rolfsii was reisolated from all necrotic crown and stem tissues. Noninoculated controls did not develop any disease symptoms. To my knowledge, this is the first report of southern blight of C. lutescens in California. This disease has been reported on areca palms and other foliage plants in the southern United States and Central and South America (1). Circumstantial evidence (the disease occurred on palm seedlings that were planted in previously unused transplant trays and new peat moss rooting medium) suggests that the pathogen may have been brought in on palm seed. In the nursery, other foliage plants that are susceptible to S. rolfsii were planted in the same rooting medium but were unaffected by southern blight. Reference: (1) A. R. Chase. Compendium of Ornamental Foliage Plant Diseases. The American Phytopathological Society. St. Paul, MN, 1987.

Plant Disease ◽  
2004 ◽  
Vol 88 (7) ◽  
pp. 769-769 ◽  
Author(s):  
S. T. Koike

Jerusalem artichoke or sunchoke (Helianthus tuberosus) is a specialty vegetable that is grown commercially in California. The fleshy tubers are harvested and used as a fresh salad ingredient or cooked vegetable. During 2003, field plantings of Jerusalem artichoke in coastal California (Santa Cruz County) showed symptoms of an unfamiliar disease. Initial symptoms consisted of wilting of new shoots and leaves followed by browning and collapse of all foliage. Crown and lower stem tissues turned tan to brown. In advanced stages of the disease, crown and stem tissues were colonized internally and externally by white, cottony mycelium. Tan, spherical sclerotia that measured approximately 1 mm in diameter formed on the surfaces of the affected crowns and stems. Mycelia and sclerotia also grew on the soil adjacent to infected plants. Isolations from symptomatic crowns, mycelia, and sclerotia produced colonies that were identified as Sclerotium rolfsii. Pathogenicity was tested using two methods that included sclerotial inocula collected from five isolates grown on potato dextrose agar plates. With the first method, sclerotia of each isolate were applied to sets of tubers (10 tubers per isolate) prior to planting tubers into a soilless, peat moss-based medium in pots. With the second method, 3-week-old potted plants were inoculated by placing sclerotia of each isolate adjacent to stem tissue that was 3 cm below the surface of the soilless medium. Noninoculated controls were included for both methods. All plants were incubated in a greenhouse at 21 to 24°C. For the first method, by the third week after planting, 10 to 40% of plants did not emerge because the tubers were rotted and decayed. For the plants that did emerge, wilting of foliage and browning of crown and stem tissue occurred approximately 6 weeks after planting and by 10 weeks, all plants were diseased. S. rolfsii was reisolated from all necrotic tuber, crown, and stem tissues. For the second method, disease symptoms and signs of the pathogen occurred 5 weeks after inoculation and by week 10, 75% of test plants were symptomatic. S. rolfsii was again reisolated from all necrotic tuber, crown, and stem tissues. Symptoms were not observed on any of the noninoculated plants. To my knowledge, this is the first report of southern blight of Jerusalem artichoke in California. This disease has been reported on Jerusalem artichoke in several southern U.S. states (1,2). The two inoculation methods demonstrated that the pathogen could infect propagation organs (tubers) and also emergent stems of this host. References: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St. Paul, MN, 1989. (2) S. M. McCarter and S. J. Kays. Plant Dis. 68:299, 1984.


Plant Disease ◽  
2003 ◽  
Vol 87 (10) ◽  
pp. 1264-1264 ◽  
Author(s):  
S. T. Koike

Corn-salad or lamb's lettuce (Valerianella locusta) is a specialty leafy green vegetable that is grown commercially in California and is harvested fresh for use in salads. In 2001, field plantings of corn-salad in coastal California showed symptoms and signs of a previously undescribed disease. Initial symptoms consisted of a light tan discoloration at the crown and lower leaf attachment areas. Once this discoloration was observed, the crown rapidly developed a soft rot, attached leaves wilted, and the entire plant collapsed. White mycelium and small (0.5 to 3.0 mm in diameter), irregularly shaped, black sclerotia formed on the crowns and lower leaves. Isolations from symptomatic crowns, mycelium, and sclerotia produced colonies of Sclerotinia minor (1). Seven-week-old corn-salad plants grown in a peat moss-based rooting medium in pots were used to test pathogenicity. Sclerotia from six corn-salad isolates from the Salinas Valley were inserted into slots made in the potting mix adjacent to the crowns of plants. Sclerotia were not placed in slots for control corn-salad. All test plants were incubated in a greenhouse at 21 to 23°C. After 4 weeks, inoculated corn-salad plants wilted and collapsed, and S. minor was reisolated from necrotic crown and stem tissues. Uninoculated plants were asymptomatic. Using the same method, sclerotia from one lettuce (Lactuca sativa) isolate were used to inoculate corn-salad plants that produced similar symptoms. All experiments were repeated and results were similar. To our knowledge, this is the first report of corn-salad as a host of S. minor in California and the United States. The susceptibility of corn-salad to S. minor from lettuce indicates that this crop might contribute to inoculum levels and lettuce drop incidence for the extensive lettuce plantings in the Salinas Valley. Reference: (1) C. L. Patterson and R. G. Grogan. Plant Dis. 72:1046, 1988.


Plant Disease ◽  
2003 ◽  
Vol 87 (12) ◽  
pp. 1539-1539
Author(s):  
C. H. Fu ◽  
H. J. Hsieh ◽  
J. C. Yao

Island ash (Fraxinus formosana Hay.) is a large, semideciduous tree in Taiwan. It is used for forestation, a shade tree, and producing wood for furniture. During the summer of 2001, a sudden wilt of 1-year-old plants was observed in a nursery in northern Taiwan. Initial symptoms included stem necrosis at the soil line and yellowing and tan discoloration of the leaves. As stem necrosis progressed, infected plants wilted and died. Necrotic tissues were covered with white mycelium that differentiated into reddish brown, spherical (1 to 2 mm in diameter) sclerotia. Sclerotium rolfsii was consistently recovered from the surface of symptomatic stem sections that were disinfected for 1 min in 0.5% NaOCl and then plated on potato dextrose agar (PDA) amended with 100 ppm of ampicillin. Pathogenicity of two S. rolfsii isolates was confirmed on 1-year-old island ash seedlings grown in 12.7 cm- (5-in) plastic pots in a sterilized mixture of peat moss and vermiculite (3:1). Seedlings were inoculated with mycelia and sclerotia of the pathogen grown on PDA. Three plants each were inoculated with four disks (5 mm) of agar with mycelium and three were inoculated with 10 sclerotia that were placed on the soil surface around the base of each plant. Noninoculated plants served as controls. All plants were kept in a growth chamber at 25 to 35°C and >95% relative humidity. The test was repeated once. All inoculated plants developed symptoms within 14 days, while control plants remained symptomless. Sclerotia developed on infected tissues, and S. rolfsii was reisolated from symptomatic tissues. This disease has been observed on many species of plants (1), but to our knowledge, this is the first report of Southern blight of Island ash seedlings caused by S. rolfsii in Taiwan. Reference: (1) Y. P. Tsai ed. List of Plant Diseases in Taiwan. The Plant Protection Society of the Republic of China and The Phytopathological Society of the Republic of China, 1991.


Plant Disease ◽  
2006 ◽  
Vol 90 (6) ◽  
pp. 829-829
Author(s):  
S. T. Koike ◽  
O. Daugovish ◽  
J. A. Downer

Celery (Apium graveolens) is grown extensively in the coastal counties (Ventura, Santa Barbara, San Luis Obispo, Monterey, and Santa Cruz) of California. In 2004 and 2005, field plantings of celery in Ventura and Monterey counties showed symptoms of a petiole and crown rot. Initial symptoms consisted of a light tan discoloration at the crowns and on outer petioles that were in contact with soil. These discolored areas developed a soft, brown, watery rot. Affected petioles wilted and later collapsed. White mycelium and small (0.5 to 3.0 mm in diameter), irregularly shaped, black sclerotia formed on diseased tissues. Isolations from symptomatic petioles, crowns, mycelium, and sclerotia produced colonies of Sclerotinia minor. Eight-week-old celery transplants (cv. Conquistador) grown in a peat-moss based rooting medium in 10-cm2 pots were used to test pathogenicity. Colonized agar plugs (one plug per plant) from eight celery isolates were inserted into slots made in the potting mix adjacent to the crowns and lower petioles of the transplants. Noncolonized plugs were placed in slots for control celery plants. Twenty plants were used for each isolate and control, and all test plants were incubated in a greenhouse at 21 to 23°C. Disease development was rapid, and after 4 days, inoculated celery plants exhibited brown necrosis at inoculation points. After 9 days, celery crowns were decayed and petioles collapsed. S. minor was reisolated from necrotic crown and petiole tissues. Noninoculated plants were asymptomatic. The experiment was repeated and results were similar. To our knowledge, this is the first report of celery as a host of S. minor in California (2). In the United States, S. minor has been reported on celery in Florida (1). Celery in California is only occasionally infected by S. minor and is more often infected by S. sclerotiorum. Reference: (1) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society. St. Paul, MN, 1989. (2) M. S. Melzer et al. Can. J. Plant Pathol. 19:272, 1997.


Plant Disease ◽  
2016 ◽  
Vol 100 (12) ◽  
pp. 2363-2369 ◽  
Author(s):  
Azin Moslemi ◽  
Peter K. Ades ◽  
Tim Groom ◽  
Pedro W. Crous ◽  
Marc E. Nicolas ◽  
...  

Pyrethrum (Tanacetum cinerariifolium) is commercially cultivated for the extraction of natural pyrethrin insecticides from the oil glands inside seed. Yield decline has caused significant yield losses in Tasmania during the last decade. A new pathogen of pyrethrum causing crown rot and reduced growth of the plants in yield decline affected fields of northern Tasmania was isolated from necrotic crown tissue and described as Paraphoma vinacea. Multigene phylogenetic identification of the pathogen also revealed that P. vinacea was a new species different from other Paraphoma type strains. Glasshouse pathogenicity experiments showed that P. vinacea significantly reduced belowground and total biomass of pyrethrum plants 2 months after inoculation. Dull-tan to reddish-brown discoloration of the cortical and subcortical crown tissue was observed in 100% of the infected plants. P. vinacea infected 75% of the plants inoculated with root dip and soil drench inoculation techniques in an inoculation optimization experiment. P. vinacea, the causal agent of Paraphoma crown rot disease, represents an important pathogen that will negatively impact the commercial cultivation of pyrethrum in Tasmania.


Plant Disease ◽  
2006 ◽  
Vol 90 (2) ◽  
pp. 246-246
Author(s):  
G. Polizzi ◽  
A. Vitale ◽  
I. Castello

Tall fescue (Festuca arundinacea Schreb.) and Kentucky bluegrass (Poa pratensis L.) are the main turfgrass species cultivated in Sicily (southern Italy) for ready lawn (sod) to ornamental purposes. In July 2004 and May 2005, a widespread disease was noticed in two turf nurseries on the eastern side of Sicily on a ready lawn mixture of F. arundinacea cv. Safari (94%) + P. pratensis cv. Cabaret (6%). Numerous yellow, circular- and crescent-shaped patches as much as 30 to 40 cm in diameter were observed. The turf usually died around the perimeter of the patch, but the grass remained green in the center of the ring with a tuft of green grass in the center (frog eye). Affected turf was initially reddish brown and turned brown as it died. Small, round and off-white or tan seed-like structures were dispersed on mycelial strands at the outer edge of the ring in the mat at the base of grasses. The pathogen was identified as Sclerotium rolfsii Sacc. The fungus was isolated directly as aerial mycelium or sclerotia or following surface disinfection (2 min in 0.5% NaOCl) and plating diseased tissues on potato dextrose agar (PDA). Sclerotia were observed in vitro in 7-day-old cultures. Pathogenicity was tested by inoculating two com-mercial ready lawn strips (80 × 100 cm) of two healthy turfgrass species each with three isolates of the fungus. Thirty sclerotia were placed at the base of stems. Noninoculated ready lawn strips served as control. All plants were covered with plastic bags, exposed to diffused daylight for 5 days, and then maintained in a growth chamber at 25 to 28°C under fluorescent light. Disease symptoms and southern blight signs like the ones observed in the field occurred 2 weeks after inoculation. S. rolfsii was reisolated from affected tissues. Symptoms were not detected on any of the non-inoculated ready lawn strips. The disease was serious enough that chemical treatments were required for its control. Southern blight was previously detected on bermudagrass and other cool-season turfgrass genera (1).To our knowledge, this is the first report of southern blight on tall fescue and bluegrass in Italy. Reference: (1) R. W. Smiley. Common Names of Plant Diseases. Diseases of Turfgrasses. Online publication. The American Phytopathological Society, St. Paul, MN.


2003 ◽  
Vol 30 (2) ◽  
pp. 120-128 ◽  
Author(s):  
K. L. Bowen

Abstract Stem rot, or southern blight, caused by the fungus Sclerotium rolfsii, is an important disease of peanut in the southeastern U.S. Incidence and apparent onset of stem rot varies from year to year depending on planting date, weather conditions, and other factors. In order to more fully understand the effects of weather on stem rot, disease progress was evaluated through the 1995, 1996, and 1997 cropping seasons. Evidence of S. rolfsii was observed on peanut roots and crowns as early as 20 d after planting (DAP), which was 1 to several wk before stem rot lesions or plant wilt were observed. Disease measures tended to be lower in 1997 than in preceding years even though more rainfall and more consistent soil moisture were noted in 1997. Soil moisture was frequently in excess of field capacity from rainfall and may have contributed to suppressing stem rot development in 1997, perhaps by limiting oxygen availability. In 1995 and 1996, rainfall patterns were more normal and irrigation contributed to greater stem rot incidence. However, low moisture, specifically 7 d with < 1.8 cm rain, was associated with increases in numbers of dead plants, perhaps due to cumulative stress from disease and lack of moisture. Areas under disease progress curves for stem rot tended to be greater for early plantings compared to late plantings. However, by ca. 118 DAP, early plantings did not consistently have a greater incidence of dead plants, probably due to environmental conditions immediately preceding that date.


Plant Disease ◽  
2007 ◽  
Vol 91 (5) ◽  
pp. 635-635 ◽  
Author(s):  
A. Pane ◽  
F. Raudino ◽  
S. Adornetto ◽  
G. Proietto Russo ◽  
S. O. Cacciola

English ivy, Hedera helix L. (Araliaceae), an evergreen climbing vine is widely cultivated as an ornamental and foliage plant. In the summer of 2005, a severe blight of ivy plants trained as topiaries and grown in an open field was observed in a nursery near Giarre (eastern Sicily). Foliage of infected plants appeared lighter green and progressively turned bronze and withered. Eventually, the entire plant collapsed. Foliar symptoms were associated with basal stem and root rot. White, cottony mycelium and numerous sclerotia developed externally on the lower stem and on the soil around the affected plants. The disease was randomly distributed, affecting approximately 5% of plants in a stock of 1,500 English ivy plants. Sclerotium rolfsii Sacc. (teleomorph Athelia rolfsii (Curzi) Tu & Kimbrough) was consistently isolated from symptomatic basal stem tissues by disinfecting in 1% NaOCl and plating on potato dextrose agar (PDA) amended with 100 mg/liter of streptomycin sulfate. The isolated fungus was identified on the basis of morphological and cultural characteristics (2). On PDA, it produced a densely, floccose, white mycelium. Mycelium was septate with clamp connections at hyphal septa. Optimum growth temperature was 30 ± 2°C. Numerous small (0.5 to 1.9 mm in diameter) sclerotia developed on the colony surface; they were spherical, occasionally slightly ellipsoidal, quite uniform in size (modal value of the diameter 1.4 mm), with a smooth surface. The surface color of the sclerotia was initially white, turned to pinkish buff, then to olive-brown, and eventually to clove brown as sclerotia matured. Sclerotia were most numerous in the center as well as close to the edge of petri dishes. Pathogenicity of one isolate obtained from infected plants was confirmed by inoculating 10 1-year-old potted English ivy plants by placing mycelium-infested wheat kernels and sclerotia on the soil surface around the collar of each plant. Ten noninoculated plants served as control. Plants were held in a dew chamber for 48 h at 28°C and subsequently placed in a greenhouse where the temperature ranged between 25 and 31°C. Plants showed wilting within 3 weeks after inoculation. Fans of white mycelium and numerous sclerotia were produced on the basal stem of inoculated test plants. Noninoculated controls remained healthy. S. rolfsii was reisolated from infected plants to fulfill Koch's postulates. English ivy has been already reported as a host of S. rolfsii, the causative agent of southern blight in nurseries of ornamentals (1). However, to our knowledge, this is the first report of southern blight on English ivy in Italy. The disease may have been favored by warm summer temperatures and overwatering with a drip irrigation system. References: (1) A. R. Chase. Compendium of Ornamental Foliage Plant Diseases. The American Phytopathological Society, St. Paul, MN, 1992. (2) J. E. M. Mordue. Corticium rolfsii. No. 410 in: Description of Pathogenic Fungi and Bacteria. CMI. Kew, Surrey, UK, 1974.


Plant Disease ◽  
2007 ◽  
Vol 91 (9) ◽  
pp. 1198-1198
Author(s):  
C. Y. Chen ◽  
C. H. Fu ◽  
W. W. Hsiao ◽  
E. J. Sun

Silvery messerschmidia, Messerschmidia argentea (L.) Johnston, of the Boraginaceae, is indigenous to Taiwan and grown as an ornamental, for windbreaks, or as a shade tree. During the summer of 2005, a sudden wilt of 1-year-old plants was observed in a nursery in central Taiwan. Initial symptoms included stem necrosis at the collar, leaf yellowing, and tan discoloration of leaves. As stem necrosis progressed, infected plants wilted, defoliated, and died. Necrotic tissues were covered with whitish mycelium with clamp connections that formed reddish brown spherical (1 to 2.2 mm in diameter) sclerotia. A fungus was consistently recovered from the interface of diseased and healthy stem tissue, disinfested for 1 min in 0.5% NaOCl, and plated on Difco (Sparks, MD) potato dextrose agar (PDA) amended with 100 ppm of ampicillin. Pure cultures were prepared by transferring single hyphal tips to PDA, and Sclerotium rolfsii (Sacc.) was identified (1). Pathogenicity of two S. rolfsii isolates was confirmed by inoculating 3-month-old silvery messerschmidia seedlings grown in pots. Inoculum consisted of a single agar disk of a 7-day-old culture used per pot or a single sclerotium produced in 10 days on PDA and added per pot. Both the mycelium on the 0.5-cm-diameter agar plug and the sclerotium touched the base of the plant stem. Four plants were inoculated with mycelia, four with sclerotia, and four were noninoculated controls. All plants were kept in a growth chamber at 25 to 35°C with relative humidity of more than 95%. Initially, the basal stems were covered by whitish mycelia growth with a fanlike pattern from the inoculum, and brown, water-soaked necrotic lesions developed near the soil line. Inoculated plants developed symptoms within 4 days, wilted gradually in 7 days, and all were eventually killed in 11 days. Plants inoculated with sclerotia developed disease at a slower rate and control plants remained symptomless. Sclerotia developed on diseased tissues and S. rolfsii was reisolated. This disease has been observed on many species of plants (2), but to our knowledge, this is the first report of southern blight of silvery messerschmidia seedlings caused by S. rolfsii in Taiwan. References: (1) R. K. Jones and D. M. Benson, eds. Diseases of Woody Ornamentals and Trees in Nurseries. The American Phytopathological Society, St. Paul, MN, 2001. (2) Y. P. Tsai, ed. List of Plant Diseases in Taiwan. The Plant Protection Society of the Republic of China and The Phytopathological Society of the Republic of China, 1991.


Plant Disease ◽  
2013 ◽  
Vol 97 (9) ◽  
pp. 1250-1250 ◽  
Author(s):  
S. T. Koike

Mexican sunflower (Tithonia rotundifolia) is a plant in the Asteraceae that is grown commercially as a cutflower commodity and also as a beneficial insectary plant. In June 2012 in coastal California (Santa Cruz County), several fields of organic lettuce (Lactuca sativa) were interplanted with direct-seeded rows of Mexican sunflower (cv. Torch) in order to attract beneficial insects. When approximately 2 to 3 weeks from harvest, lettuce plants began to wilt and collapse. Lettuce crowns were decayed and covered with white mycelium and small (0.5 to 3 mm diameter), irregularly shaped, black sclerotia. These plants were confirmed to have lettuce drop disease caused by Sclerotinia minor (2). In addition, Mexican sunflower plants began to wilt and eventually died. Initial symptoms on crowns and bases of the main stems in contact with soil consisted of a light tan discoloration. These discolored areas turned darker brown, became necrotic, and later were covered with white mycelium and sclerotia that were identical to those found on lettuce. Symptomatic sunflower stems were surface disinfested and small pieces from the margins of necrotic areas were placed into petri plates containing acidified potato dextrose agar. Resulting fungal colonies were white, produced profuse numbers (approx. 39 sclerotia/cm2) of small black sclerotia, and were identified as S. minor. Six-week-old Mexican sunflower plants grown in a peat moss-based rooting medium in 5-cm square pots were used to test the pathogenicity of four isolates. Isolates were grown on cubed and autoclaved potato pieces and resulting sclerotia were recovered and dried (1). For each isolate, 12 plants for each of three cultivars (cvs. Fiesta del Sol, Torch, and Yellow Torch) were inoculated by placing 3 to 5 sclerotia 1 cm below the soil level and adjacent to the plant crowns/stem bases. Sterile sand was placed next to crowns of the control plants. Plants were maintained in a greenhouse at 22 to 24°C. Symptom development was rapid and after 6 to 7 days, inoculated Tithonia plants exhibited brown necrosis at inoculated areas. After 10 days, Tithonia crowns were decayed and plants wilted. S. minor was reisolated from selected necrotic crown and stem tissues. Diseased plants that were not used for reisolations later supported the growth of the characteristic white mycelium and black sclerotia. There were no significant differences between the Tithonia cultivars, and overall disease incidence ranged from 74 to 100%. Non-inoculated plants were asymptomatic. The experiment was repeated and results were similar. In addition, the sclerotia of the four Tithonia isolates were similarly inoculated onto sets of 12 romaine lettuce plants (cv. Green Towers). After 5 to 6 days, all plants developed lettuce drop disease and the pathogen was reisolated. To my knowledge, this is the first report of Mexican sunflower as a host of S. minor. These findings indicate that Mexican sunflower and lettuce are susceptible to the same lettuce drop pathogen, and that this beneficial insectary plant could increase soilborne inoculum of S. minor. Growers should therefore be aware of the host status of beneficial insectary and other plants interplanted with crops. References: (1) P. Chitrampalam et al. Phytopathology 101:358, 2011. (2) K. V. Subbarao. Plant Dis. 82:1068, 1998.


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