scholarly journals First Report of Powdery Mildew Caused by an Oidium sp. on Papaver nudicaule in Italy

Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Iceland poppy (Papaver nudicaule L.) is grown on the Italian Riviera for export as a cut flower and its importance in the industry is increasing. During the spring of 2003, severe outbreaks of powdery mildew that had not been reported previously, occurred in several commercial plantings grown outdoors in containers near Imperia in northern Italy. Mycelium was observed on all green organs of the plant (leaves, stems, and petioles). Both surfaces on the leaves were affected, and heavily colonized leaves were distorted. As the disease progressed, diseased leaves turned yellow and died. The disease did not affect the flowers. Conidia were hyaline, cylindric, and measured 10.8 to 29.8 × 16.8 to 48.0 μm (average 13.7 × 37.3 μm). Foot cells were cylindric and appressoria unlobed. Fibrosin bodies were not present, and cleistothecia were not observed. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1,2). Pathogenicity was confirmed by gently pressing leaves with visible sporulation onto the leaves of five 90-day-old P. nudicaule plants that were healthy and free of symptoms. Five noninoculated healthy plants served as controls. Inoculated and noninoculated plants were maintained in a growth chamber at 15°C with a 12-h photoperiod. After 7 to 10 days, typical symptoms of powdery mildew developed on inoculated plants but not on noninoculated plants. Previously, Erysiphe cruciferarum Opiz ex L. Junell has been reported on P. nudicaule in all continents, and E. cichoracearum DC. and E. polygoni DC. have been reported in several countries, including Italy, as a causal agent of powdery mildew on other species of Papaver including P. rhoeas and P. strigosum. To our knowledge, this is the first report of powdery mildew caused by an Oidium sp. on P. nudicaule in Italy. The voucher specimen is kept in the department collection at the University of Torino. References: (1) R. Belanger et al., eds. The Powdery Mildew A Comprehensive Treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia. 89:700, 1987.

Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Salvia scabra Thunb. is grown and used on the Italian Riviera as a potted plant and used in gardens. During the spring of 2003, severe outbreaks of a previously unknown powdery mildew were observed in a collection of Salvia spp. maintained at an experimental station at Albenga (northern Italy). Powdery mildew was observed only on S. scabra. Leaves were covered with white exophytic mycelia on both surfaces. As the disease progressed, infected leaves turned yellow and died. Conidia were single, hyaline, cylindric, and measured 21.3 to 35.5 × 12.5 to 22.5 μm (average 28.2 × 18.4 μm). Observations made with a light microscope revealed that foot cells were cylindric and appressoria lobed. Cleistothecia were not observed. The pathogen was identified as Oidium subgenus Pseudoidium (1,2), and pathogenicity was confirmed by gently pressing diseased leaves onto mature leaves of healthy, 40-day-old S. scabra plants. Five plants of S. scabra were used as replicates. Noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a growth chamber at 20°C. After 5 days, typical symptoms of powdery mildew developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on S. scabra in Italy as well as in the world. Erysiphe polygoni DC. (Oidium subgenus Pseudoidium) and E. cichoracearum DC. (Oidium subgen us Reticuloidium) were previously reported as causal agents of powdery mildew on other species of Salvia (S. officinalis and S. sclarea) (3,4). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) R. Belanger et al., eds. The Powdery Mildew A Comprehensive Treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia. 89:700, 1987. (3) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (4) A. Pisi and M. G. Bellardi. Inf. Fitopatol. 48(10):57, 1998.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
M. L. Gullino

Mandevilla splendens (Hook.) Woodson is a tropical plant belonging to the Apocynaceae family and grown in Italy as an ornamental. It is generally potted and used to create small barriers on terraces and gardens. During February 2003, severe outbreaks of a previously unknown powdery mildew were observed in a commercial glasshouse located at Albenga (northern Italy) where 30% of the plants were affected by the disease. Infected young leaves were covered on both sides with white mycelia. Mycelia were more evident on the lower surface of older leaves. As the disease progressed, infected leaves turned reddish and eventually became yellow and died. Powdery mildew infections sometimes cause leaves to distort and have reduced growth. Conidia were hyaline, ellipsoid or cylindrical, sometimes appeared to adhere in chains, measured 9 to 15 × 14 to 28 μm (average 12 × 21 μm), and did not show fibrosin bodies. Foot cell was cylindric and appressorium lobed. Cleistothecia were not observed. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1,2,3). Pathogenicity was confirmed by gently pressing diseased leaves onto young leaves of healthy, 1-year-old M. splendens plants grown in 3.5 liter pots. Three plants were inoculated, while three noninoculated plants served as controls. After inoculation, plants were maintained in a growth chamber at 18°C (12-h light, relative humidity >75%). After 60 days, powdery mildew symptoms were observed on inoculated plants. Noninoculated plants remained healthy. The pathogenicity test was carried out twice. To our knowledge, this is the first report of powdery mildew on M. splendens in Italy, as well as in the world. Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) R. Belanger et al., eds. The powdery mildew A comprehensive treatise. The American Phytopathological Society, St Paul, MN, 2002. (2) U. Braun. Nova Hedwigia, 89:700, 1987. (3) R. T. A. Cook et al. Mycol. Res. 101:975, 1997.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 681-681
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Aquilegia flabellata Sieb. and Zucc. (columbine) is a perennial garden species belonging to the family Ranunculaceae. During the summer of 2003, a severe outbreak of a previously unknown powdery mildew was observed in several gardens near Biella (northern Italy). Upper surfaces of leaves were covered with a white mycelium and conidia, and as the disease progressed infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia were hyaline, ellipsoid, and measured 31.2 to 47.5 × 14.4 to 33 μm (average 38.6 × 21.6 μm). Fibrosin bodies were not present. Cleistothecia were globose, brown, had simple appendages, ranged from 82 to 127 (average 105) μm in diameter, and contained one to two asci. Ascocarp appendages measured five to eight times the ascocarp diameter. Asci were cylindrical (ovoidal) and measured 45.3 to 58.2 × 30.4 to 40.2 μm. Ascospores (three to four per ascus) were ellipsoid or cylindrical and measured 28.3 to 31.0 × 14.0 to 15.0 μ;m. On the basis of its morphology, the pathogen was identified as Erysiphe aquilegiae var. aquilegiae (1). Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of five, healthy A. flabellata plants. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a garden where temperatures ranged between 20 and 30°C. After 10 days, typical powdery mildew symptoms developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on Aquilegia flabellata in Italy. E. communis (Wallr.) Link and E. polygoni DC. were reported on several species of Aquilegia in the United States (2), while E. aquilegiae var. aquilegiae was previously observed on A. flabellata in Japan and the former Union of Soviet Socialist Republics (3). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Nova Hedwigia, 89:700, 1987. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society, St Paul, MN, 1989. (3) K. Hirata. Host Range and Geographical Distribution of the Powdery Mildews. Faculty of Agriculture, Niigata University, 1966.


Plant Disease ◽  
2014 ◽  
Vol 98 (7) ◽  
pp. 1013-1013 ◽  
Author(s):  
I. Y. Choi ◽  
B. S. Kim ◽  
S. E. Cho ◽  
J. H. Park ◽  
H. D. Shin

Gypsophila paniculata L. (baby's breath, family Caryophyllaceae), native to Central and Eastern Europe, is commonly cultivated as a commercial cut flower crop in greenhouses in Korea. Since 2011, baby's breath cv. Cassiopeia has been observed affected by a powdery mildew with nearly 100% disease incidence at the stage of harvesting in Iksan City. Powdery mildew colonies first appeared as thin white patches on stems and both sides of the leaves. As disease progressed, plants were covered with dense masses of spores, followed by senescence and reduction of quality of cut flowers. A voucher specimen was deposited in the Korea University Herbarium (Accession KUS-F27313). Appressoria were well-developed, multilobed or moderately lobed, and single or opposite in pairs. Conidiophores were straight, 95 to 150 × 7 to 10 μm, and composed of 3 to 4 cells. Foot-cells were cylindric or slightly sinuous at the base and 37 to 53 μm long. Singly produced conidia were cylindrical to oblong-elliptical, 35 to 56 × 12.5 to 18 μm with a length/width ratio of 2.1 to 3.6, devoid of fibrosin bodies, and with angular/rectangular wrinkling of outer walls. Germ tubes were in the perihilar position on conidia, and ended with lobed appressoria. No chasmothecia were found. These structures are typical of the Pseudoidium anamorph of the genus Erysiphe. Specific measurements and host range were consistent with those of E. buhrii U. Braun (2). To confirm identification, the complete internal transcribed spacer (ITS) region of rDNA of isolate KUS-F27313 was amplified with primers ITS1/ITS4, and sequenced directly. The resulting 725-bp sequence was deposited in GenBank (KJ530705). A GenBank BLAST search of the Korean isolate showed 99% similarity with E. buhrii on Acanthophyllum sp. (Caryophyllaceae) from Iran (AB128924). Pathogenicity was confirmed through inoculation by gently dusting conidia onto leaves of five healthy, potted baby's breath cv. Cassiopeia. Five non-inoculated plants served as controls. Inoculated plants were isolated from non-inoculated plants in separate rooms in a greenhouse at 25 ± 2°C. Inoculated plants developed signs and symptoms after 7 days, whereas the control plants remained symptomless. The fungus present on the inoculated plants was identical morphologically to that originally observed on diseased plants. Pathogenicity test was repeated twice. The powdery mildew disease caused by E. buhrii on baby's breath has been recorded in the former Soviet Union (Armenia, Kazakhstan, Ukraine), Romania, Turkey, Iran, Mongolia, and Argentina (1,3). Also, a fungus occurring on baby's breath was recorded as Oidium sp. from Japan (4). To our knowledge, this is the first report of powdery mildew caused by E. buhrii on baby's breath in Korea. Powdery mildew infections pose a serious threat to production of this cut flower crop. References: (1) K. Amano. Host Range and Geographical Distribution of the Powdery Mildew Fungi. Japan Scientific Societies Press, Tokyo, 1986. (2) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No. 11. CBS, Utrecht, 2012. (3) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved February 18, 2014. (4) M. Satou et al. Ann. Phytopathol. Soc. Jpn. 62:541, 1996.


Plant Disease ◽  
2004 ◽  
Vol 88 (9) ◽  
pp. 1045-1045
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Honeysuckle (Lonicera caprifolium L., family Caprifoliaceae) is a climbing shrub used in gardens to cover walls and supports. During the summer of 2003, severe outbreaks of a previously unknown powdery mildew were observed on this species in some gardens near Biella (northern Italy). The first symptoms included extensive chlorosis on leaves, followed by the appearance of white mycelium on the adaxial and abaxial leaf surfaces. As the disease progressed, infected leaves turned yellow and died. Conidia were hyaline, ellipsoidal, and measured 27.6 to 43.2 × 12.2 to 21.6 μm (average 35.7 × 17.6 μm). Foot cells were cylindric and appressoria lobed. Fibrosin bodies were not present. Cleistothecia were not observed during the growing season. The pathogen was identified as Oidium subgenus Pseudoidium (2). The inoculation procedure involved gently pressing diseased leaves onto leaves of healthy L. caprifolium plants. Three plants of L. caprifolium were used as replicates. Noninoculated plants served as control. Inoculated and noninoculated plants were maintained in a garden at temperatures ranging from 15 to 25°C. After 10 days, typical symptoms of powdery mildew developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of powdery mildew on L. caprifolium in Italy. The presence of powdery mildew on different species of Lonicera has been reported in several countries, particularly, Microsphaera miurae U. Braun on L. morowii A. Gray in Germany (1), M. lonicerae (DC.) Winter on L. peryclimenum L. in England (3), and M. lonicerae-ramosissimae on L. ramosissima Fr. & Sav. in Japan (4). The conidia of M. lonicerae are smaller than those of the Oidium sp. reported on L. caprifolium. Voucher specimens are available at DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Mycotaxon 16:417, 1983. (2) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (3) J. Robbins. Cecidology 15:15, 2000. (4) S. Tanda. Mycoscience 41:155, 2000.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 682-682
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Akebia quinata Decne., an ornamental species belonging to the family Lardizabalaceae, is used as a climbing species in gardens to cover walls as well as supports and is very much appreciated because of its dark red flowers. During the summer of 2003, severe outbreaks of a previously unknown powdery mildew were observed on established plantings in several gardens near Biella (northern Italy). The upper surfaces of leaves were covered with white mycelium, and the corresponding abaxial surface of infected leaves were chlorotic. Young, green stems also affected showed extended chlorosis. As the disease progressed, infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia formed singly were hyaline, ellipsoid, and measured 26.4 to 45.6 × 10.6 to 15.6 μm (average 35.1 × 12.7 μm). Fibrosin bodies were not present. The pathogen was identified as Oidium sp. subgenus Pseudoidium (1) partially because cleistothecia were not observed. Conidial measurements are close to those reported for Microsphaera akebiae Sawada. Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of healthy A. quinata plants. Three plants of A. quinata were used as replicates. Noninoculated plants served as controls. Plants were maintained between 20 and 30°C in a garden located 5 km from where the disease was originally found. After 10 days, typical symptoms of powdery mildew developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on A. quinata in Italy. The disease is currently restricted to the area of Biella. The presence of M. akebiae was recently reported in the Netherlands (2). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun and S. Takamatsu. Schlechtendalia, 4:1, 2000. (2) M. Scholler and W. Gams. Nova Hedwigia, 67:101, 1998.


Plant Disease ◽  
2000 ◽  
Vol 84 (6) ◽  
pp. 705-705 ◽  
Author(s):  
G. S. Saenz ◽  
S. T. Koike ◽  
H. J. Scheck

Nandina domestica Thunb. (heavenly bamboo) is an ornamental plant that is widely planted in landscapes in California and other states. Since 1996, powdery mildew disease has been seen on outdoor landscape N. domestica in various regions of California (Alameda, Monterey, Riverside, and Santa Barbara counties). Symptoms consist of reddening of leaf and stem tissues colonized by the fungus and curling and twisting of infected leaves. The following observations were the same for all collected isolates. White ectophytic mycelium was observed on leaves and petioles. Mycelium on leaves was amphigenous, mostly epiphyllous, and effused or in patches. Hyphal appressoria were nipple-shaped to lobed and sometimes opposite in orientation. Conidiophores were cylindrical, straight, sometimes slightly flexuous, 22 to 32 × 6 to 8 μm in dimension, and followed by one to two shorter cells. Conidia were cylindrical, produced singly, and 27 to 42 × 11.5 to 14 μm in dimension. Fibrosin bodies were not observed. Conidial germ tubes were approximately twice the length of the spore, originated from the ends of the spore, and terminated in simple appressoria. Cleistothecia were not present. Based on these characteristics, the fungus was identified as Microsphaera berberidis (DC) Lév. (1). Pathogenicity was confirmed by gently pressing diseased leaves on leaves of healthy N. domestica plants. Plants were incubated in a humidity chamber at 22 to 24°C, and after 10 to 14 days, powdery mildew colonies developed. A voucher specimen was deposited in the University of California Herbarium (UC 1738622). Additional inoculation experiments showed that four other N. domestica cultivars were susceptible (Compacta Nana, Gulf Stream, Harbour Dwarf, and Royal Princess). Helfer (2) noted several possible candidates for the Nandina powdery mildew pathogen in the United Kingdom. However, due to the conidial characteristics of that fungus and the paucity of character descriptions for the several species mentioned, no species name was given to the Edinburgh isolate. In contrast, the mitosporic characteristics of our isolates fit the description for M. berberidis. This is the first report of powdery mildew on N. domestica in North America. References: (1) U. Braun. Nova Hedwigia 89:1, 1987. (2) S. Helfer. Plant Dis. 79:424, 1995.


Plant Disease ◽  
2014 ◽  
Vol 98 (3) ◽  
pp. 421-421 ◽  
Author(s):  
H. H. Zhao ◽  
H. H. Xing ◽  
C. Liang ◽  
X. Y. Yang ◽  
S. E. Cho ◽  
...  

Chinese cabbage, Brassica rapa ssp. pekinensis (syn. Brassica pekinensis (Lour.) Rupr.), in the Brassicaceae, is an important vegetable grown on about 3 million ha in China. Since 2012, a powdery mildew has been found infecting Chinese cabbage plants (cv. Qingyanchunbai No. 1) after bolting for seed production from autumn through spring 2013 in a greenhouse in Qingdao, China. Symptoms first appeared as circular to irregular white patches on both sides of the leaves, and on stems and pods, often thinly covering the whole surface. A voucher specimen was deposited in the herbarium of Qingdao Agricultural University (Accession No. HMQAU12216). Hyphae were thin-walled, smooth, hyaline, and 4 to 6 μm wide. Appressoria on the mycelia were well developed, lobed, solitary, or in pairs. Conidiophores were erect, cylindrical, 45 to 110 μm long, and comprised 3 to 4 cells. Foot-cells of conidiophores were straight, cylindrical, 16 to 28 μm long, and 7.6 to 10 μm wide. Singly-produced conidia were oblong to cylindrical or somewhat ellipsoid-doliiform, 32 to 56 × 12 to 18 μm, with a length/width ratio of 1.8 to 3.8, with angular/rectangular wrinkling of the outer wall surface, and lacked distinct fibrosin bodies. Germ tubes were produced in the perihilar position of conidia. No chasmothecia were found. These structures are typical of the powdery mildew Pseudoidium anamorph of Erysiphe (2). The specific measurements and characteristics (especially short foot-cells of conidiophores) were consistent with previous records of Erysiphe cruciferarum Opiz ex L. Junell (2,3). To confirm the identification, the complete internal transcribed spacer (ITS) region of rDNA of isolate HMQAU12216 was amplified (4) and sequenced directly. The resulting 649-bp sequence was deposited in GenBank (Accession No. KC878683). A GenBank BLAST search of ITS sequences showed an exact match with those of E. cruciferarum on B. oleracea var. acephala (GU721075) and Oidium sp. on B. pekinensis (AB522714). A pathogenicity test was conducted by gently pressing a symptomatic leaf loaded with conidia onto a leaf of each five, healthy, potted, 40-day-old plants (cv. Qingyanchunbai No. 1). Five non-inoculated plants served as a control treatment. Inoculated plants were isolated from non-inoculated plants in separate rooms in a greenhouse at 20 ± 2°C. Inoculated plants developed signs and symptoms after 10 days, whereas the control plants remained symptomless. The fungus present on the inoculated plants was identical morphologically to that originally observed on diseased plants, thus fulfilling Koch's postulates. Though many Brassica spp. have been known to be infected with E. cruciferarum throughout the world, powdery mildew of Chinese cabbage caused by E. cruciferarum has been reported only in Finland, Germany, and Korea (1,3). To our knowledge, this is the first report of powdery mildew caused by E. cruciferarum on Chinese cabbage in China. Though occurrence of the powdery mildew on Chinese cabbage was noticed in an experimental breeding plot, this finding poses a potential threat to production of this vegetable in China. References: (1) U. Braun. The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Jena, Germany, 1995. (2) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No. 11. CBS, Utrecht, 2012. (3) H. J. Jee et al. Plant Pathol. 57:777, 2008. (4) S. Matsuda and S. Takamatsu. Mol. Phylogen. Evol. 27:314, 2003.


Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 432-432 ◽  
Author(s):  
P. Jimenez ◽  
T. A. Zitter

In early August 2004, pumpkin and zucchini squash (Cucurbita pepo) plants grown in conventional and organic commercial operations in Orange and Dutchess counties, respectively, showed spindle-shaped lesions on vegetative tissues and silver russeting and spots on fruit, typical of Plectosporium blight. Approximately 20% of pumpkin fruit were affected at this early time in yield development, while the zucchini planting had been abandoned due to disease. Symptomatic pieces of stem, petioles, and main leaf veins were excised, surface disinfected with 0.5% sodium hypochlorite, placed on one-quarter-strength potato dextrose agar, and incubated at 21°C with a 12-h photoperiod. Pale pink colonies with pinkish, hyaline, aerial mycelium developed from the tissues. When examined microscopically, simple and branched conidiophores with apical phialides were observed, as well as non- and one-septate ellipsoidal to slightly curved conidia that measured 7.5 to 13.0 × 2.5 to 3.3 μm. The fungus fits the description of Plectosporium tabacinum (van Beyma) M.E. Palm, W. Gams, & H.I. Nirenberg (synonyms Microdochium tabacinum (von Arx, 1984) and Fusarium tabacinum (Gams & Gerlagh, 1968) (1). Pathogenicity was tested on 10 seedlings each of pumpkin, zucchini, gourd (C. pepo), winter squash (C. moschata), and cucumber (Cucumis sativa). Plants were spray inoculated at the three true-leaf stage with a spore suspension at 104 conidia/ml in water with 1% gelatin. Plants were held overnight in a moist chamber and then transplanted into 12-cm-diameter pots and kept in the greenhouse for the rest of the experiment. P. tabacinum was reisolated from all inoculated plants which completes Koch's postulates. Symptoms were noted 3 days after inoculation on pumpkin, zucchini, and gourd, with typical spindle-shaped lesions on the main stem, petioles, and main leaf veins (2). Symptoms developed after 1 week on winter squash, and lesions were mostly concentrated on the older portion of the stem with occasional lesions on the petiole and main leaf veins. Symptoms on cucumber, however, did not develop until 2 weeks after inoculation and appeared as an inconspicuous line of coalesced lesions on the ridges of the main stem only. These symptoms could easily be misidentified as physical abrasions from handling or from wind scarring. These results confirm the high susceptibility of C. pepo species, and indicate that other cucurbits are susceptible, albeit at a lower level. To our knowledge, this is the first report of P. tabacinum in New York. A voucher specimen has been deposited in the Cornell Plant Pathology Herbarium (Accession No. CUP 67504). References: (1) M. E. Palm et al. Mycologia 87:397, 1995; (2) T. A. Zitter. Microdochium blight. Page 28 in: Compendium of Cucurbit Diseases. T. A. Zitter, D. L. Hopkins, and C. E. Thomas, eds. The American Phytopathological Society, St. Paul, MN, 1996.


Plant Disease ◽  
2002 ◽  
Vol 86 (8) ◽  
pp. 920-920
Author(s):  
A. Garibaldi ◽  
A. Minuto ◽  
D. Bertetti ◽  
M. L. Gullino

Euryops pectinatus is grown in Italy for landscape use in parks and gardens. In 2001, severe outbreaks of a previously unknown powdery mildew were observed in commercial farms located in Albenga (northern Italy). All green parts (leaves, stems, and petioles) became covered with a white mycelium. Infections were particularly severe on the upper leaf surface. With progress of the disease, infected leaves turned yellow and died. The presence of powdery mildew infections on leaves and stems only rarely was linked to growth reduction. Conidia were hyaline, cylindric to slightly doliform, did not show fibrosin bodies, borne in chains, and measured 24 to 41 × 12 to 20 μm. Cleistothecia were not observed. The pathogen was identified as Oidium sp. subgen. Fibroidium (1). Pathogenicity was confirmed by gently pressing diseased leaves on leaves of healthy E. pectinatus plants. Inoculated plants were maintained in a growth chamber at 20 to 24°C. After 12 to 14 days, powdery mildew symptoms developed. A similar disease of E. pectinatus was observed in 1999 in California and identified as being caused by Podosphaera (Sphaerotheca) fusca (2). It is possible that the powdery mildew observed in Italy belongs to the same species, also considering that recently the two genera, Podosphaera and Sphaerotheca, have been unified in the genus Podosphaera (1). References: (1) U. Braun and S. Takamatsu. Schlechtendalia 4:1, 2000. (2) G. S. Saenz et al. Plant Dis. 84:1048, 2000.


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