Microsphaera penicillata. [Descriptions of Fungi and Bacteria].

Author(s):  
K. G. Mukerji

Abstract A description is provided for Microsphaera penicillata. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On species of Alnus, Betula, Syringa, Lathyrus, sweet peas and numerous other hosts (Saknon, 1900; Stevens, 1925; 39: 739; 41: 175) DISEASES: Powdery mildew of alder and lilac. Forms a white to grey floury appearance on the surface of broad leaves of many hard wood trees. It is more prevalent on sweet peas than Erysiphe pisi (CMI Descript. 155) in North America in spring when temperature and humidity are fluctuating. The foliage may be malformed, dropping prematurely or drying out and shrivelling. It is also prevalent on lilac in late summer and autumn, sometimes in dry seasons almost completely covering the foliage, but generally too late in the season to cause serious damage. Young leaves are more susceptible. GEOGRAPHICAL DISTRIBUTION: World-wide on alder and lilac and occasionally occurring on numerous other hosts. Distributed generally in North America and Europe, also reported from Chile, China, India and Japan (Salmon, 1900, 39: 739; 41: 175). TRANSMISSION: Spores wind borne.

Author(s):  
J. N. Kapoor

Abstract A description is provided for Erysiphe pisi. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Papilionaceae, chiefly on Pisum, Dorcynium, Medicago and Vicia; also on Lupinus spp., Lens esculenta[Lens culinaris], Trifolium dubium and? Astragalus alpinus (Blumer, 1967). DISEASE: Powdery mildew of pea. GEOGRAPHICAL DISTRIBUTION: World-wide. TRANSMISSION: Internally seed borne (15: 338).


Author(s):  
J. N. Kapoor

Abstract A description is provided for Podosphaera leucotricha. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Malus spp., chiefly on M. pumila (apple), peach (Prunus persica), quince (Cydonia ualgaris) and Photinia spp. also attacked (Hirata, 1966). Also reported on almond fruit (43, 2544). DISEASE: Powdery mildew of apple. GEOGRAPHICAL DISTRIBUTION: Africa (? Kenya, Rhodaia, South Africa, Tanzania); Asia (China, India, Israel, Japan, U.S.S.R.); Australia and New Zealand, Europe (widely distributed) North America (Canada and U.S.A.); South America (Argentina, Brazil, Chile, Colombia, Peru). (CMI map 118). TRANSMISSION: Overwinters on host as dormant mycdium in blossom buds. The role of deistothecia in overwintering is doubtful. Spread by wind-borne conidia (Anderson, 1956).


Author(s):  
P. M. Stockdale

Abstract A description is provided for Nannizzia obtusa. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Primarily a pathogen of the pig, occasionally transmitted to man. Guinea-pigs have been experimentally infected. DISEASE: Ringworm (dermatophytosis, tinea). In pigs lesions are circular and circumscribed to irregular in outline, sometimes involving almost the whole body. They are reddish in colour and are frequently covered with brownish crusts. Alopecia and pruritis do not occur (RMVM 5, 226, 491-492). In man the scalp (tinea capitis) and glabrous skin (tinea corporis) may be infected. Scalp lesions reported have shown a kerion type of reaction with endothrix hair invasion; in some cases infected hairs have fluoresced light green under Wood's light. GEOGRAPHICAL DISTRIBUTION: Reported from Africa (Kenya), Australasia (Australia, New Zealand); North America (Canada, U.S.A. (Ind., Kans., Ky, Miss., N.J., Pa)), Central America and West Indies (Mexico, Cuba). Possibly world-wide in distribution.


Author(s):  
B. C. Sutton

Abstract A description is provided for Dibotryon morbosum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Prunus americana, P. armeniaca, P. avium, P. besseyi, P. cerasus, P. domestica, P. maritima, P. melanocarpa, P. pennsylvanica, P. pumila, P. serotina, P. virginiana and other species of Prunus. DISEASE: Black knot of plum, damson, cherry, peach, apricot and other species of Prunus. The pathogen causes the formation of elongated black hypertrophied host tissue on the current year's branches or on trunks. These are generally confined to one side and are several times the normal diameter of the stem. The knots are olive-green and corky at first, later turning black and becoming hard and brittle. In late summer some may appear pink or white due to parasitism by Trichothecium roseum. On black cherry, P. serotina, large cankerous swellings 0.6 m or more long may be formed which render the tree worthless for timber. Attacked trees become stunted and dwarfed. GEOGRAPHICAL DISTRIBUTION: Confined to North America (Canada and U.S.A.) (CMI Map 48). TRANSMISSION: By ascospores which have a peak production in May (45, 3263h). Storage of knots from Prunus serotina at -20°C for 6 months had little effect on ascospore viability (44, 2699j). Conidia also tolerate low temperatures, surviving 192 days at -20°C but only 25 days at 21°C (47, 573). In addition to some conidia overwintering in a viable condition on plum and cherry, others develop from overwintering chlamydospores on plum buds and bark (14: 43). Prunings containing excised knots which are left lying in orchards can continue to produce viable spores for several weeks after being removed (9: 116; 24: 375). The pathogen may also be introduced to new areas on infected nursery stock (McClintock, 1945).


Author(s):  
J. N. Kapoor

Abstract A description is provided for Sphaerotheca fuliginea. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On numerous genera of Compositae, Cucurbitaceae and Scrophulariaceae. Also on Helianthemum spp. (Cistaceae); Arabis spp., Braya spp., Capscila spp., Cardaminc spp., Draba spp., Parrya spp. (Cruciferae); Dipsacus spp. (Dipsacaceae); Astragalu, spp., Glycine max, Phascolus spp., Rhynchosia spp., Vigna spp.(Leguminosae); Plantago spp. (Plantaginaceae); Hibiscus esculentus (Malvaceae); Hyoscyarnus niger, Mandragora officinalis, Petunia spp., Physalis spp., Solanum melongena (Solanaceae). (Blumer, 1967; Hirata, 1966). DISEASE: Powdery mildew of cucurbits. GEOGRAPHICAL DISTRIBUTION: World-wide. TRANSMISSION: Not known.


Author(s):  
K. G. Mukerji

Abstract A description is provided for Leveillula taurica. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Gossypium barbadense, G. hirsutum and Cyamopsis psoraloides[Cyamopsis tetragonoloba]. Also on many other trees and shrubs belonging to the Leguminoseae, Malvaceae and Euphorbiaceae (Salmon, 1900; Blumer, 1933; Tarr, 1955; 37: 521). DISEASES: Powdery mildew of cotton and guar. The host becomes completely covered with the fungus which mostly forms conidia and rarely cleistothecia. Severe attacks cause defoliation. Komarov (1895) reported that in Seravschan-Turkestan every plant of the steppes up to 1219-1524 m is attacked. The fungus does not occur beyond 1829 m. GEOGRAPHICAL DISTRIBUTION: World wide but mainly in the mediterranean region, Central Europe and the Near East (Dennis, 1960; CMI Map 217; 37: 400). TRANSMISSION: Wind borne. In the Sudan the pathogen over-summers on Euphorbia heterophylla, a common weed (37: 521).


Plant Disease ◽  
2013 ◽  
Vol 97 (6) ◽  
pp. 843-843 ◽  
Author(s):  
Y. J. La ◽  
S. E. Cho ◽  
H. D. Shin

Platanus occidentalis L., called American sycamore or American plane, is native to North America. The trees are commonly planted throughout the world on the sides of roads and in parks. In June 2012, diseased leaves exhibiting signs of powdery mildew from a park in Daegu City of Korea were sent to Plant Clinic of Seoul National University for diagnosis. Our observations in Daegu City during September and October 2012 showed that nearly 99% of the approximately 1,000 trees surveyed were infected with a powdery mildew. Voucher specimens (n = 6) were deposited at the Korea University Herbarium (KUS). Symptoms were characterized by chlorosis, distortion, or cupping of young leaves. White superficial colonies developed amphigenously on leaves. Hyphae were flexuous to straight, branched, septate, 4 to 7 μm wide, and had lobed appressoria. Conidiophores were 120 to 350 × 5 to 7.5 μm and produced conidia singly. Foot-cells of conidiophores were straight, cylindric, and 115 to 200 μm long. Conidia were hyaline, ellipsoid-ovoid, measured 33 to 47.5 × 17.5 to 29 μm with a length/width ratio of 1.5 to 2.0, lacked distinct fibrosin bodies, and showed reticulate wrinkling of the outer walls. Germ tubes were produced on the subterminal position of conidia. No chasmothecia were observed. The structures and measurements were compatible with those of the anamorphic state of Erysiphe platani (Howe) U. Braun & S. Takam. (1). To confirm the identification, the complete internal transcribed spacer (ITS) region of the rDNA from isolate KUS-F26959 was amplified with nested PCR and sequenced. The resulting sequence of 625 bp was deposited in GenBank (Accession No. JX997805). A GenBank BLAST search of this sequence showed only one base substitution with the four sequences (JQ365940 to JQ365943) of E. platani on Platanus spp. Pathogenicity was confirmed through inoculation tests by gently pressing diseased leaves onto young leaves of three 2-year-old disease-free seedlings. Three non-inoculated plants were used as control. Plants were maintained in a greenhouse at 24 to 30°C. Inoculated leaves developed symptoms after 7 days, whereas the control plants remained symptomless. The fungus present on the inoculated leaves was morphologically identical to that observed on the original diseased leaves, fulfilling Koch's postulates. Since E. platani first was recorded in the United States in 1874, it has been regarded as endemic in North America. From the second half of the 20th century, introduction and expansion of the range of this fungus to South America, South Africa, Australia and New Zealand, Europe, and Asia have been reported (1,2). To our knowledge, this is the first report of E. platani infections of P. occidentalis in Korea. This species was recorded on P.× hispanica from Japan in 1999 (4) and on P. orientalis from China in 2006 (3), suggesting invasive spread of the sycamore powdery mildew in East Asia. Since American sycamores are widely planted in Korea, control measures should be made to prevent further spread of the disease. References: (1) U. Braun and R. T. A. Cook. Taxonomic Manual of the Erysiphales (Powdery Mildews), CBS Biodiversity Series No.11. CBS, Utrecht, 2012. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Syst. Mycol. Microbiol. Lab., Online publication, ARS, USDA, Retrieved October 22, 2012. (3) C. Liang et al. Plant Pathol. 57:375, 2008. (4) S, Tanda. J. Agric. Sci., Tokyo Univ. Agric. 43:253, 1999.


Author(s):  
J. N. Kapoor

Abstract A description is provided for Uncinula necator. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Vitis spp., chiefly Vitis vinifera; also on Parthenocissus spp., Ampelopsis spp. DISEASE: Powdery mildew of vine. GEOGRAPHICAL DISTRIBUTION: World-wide. TRANSMISSION: Conidia and mycelium overwinter in diseased buds, fallen berries or on overwintered stems. Cleistothecia, when formed, are capable of overwintering (Blumer, 1967).


1951 ◽  
Vol 29 (1) ◽  
pp. 1-16 ◽  
Author(s):  
L. P. E. Choquette

The systematic position of the genus Rhabdochona Railliet, 1916 and its diagnosis is reviewed. The genus comprising 33 species has a world-wide distribution and has been found, with one exception, in fish. Species from fish in North America are discussed and R. cascadilla Wigdor, 1918 is redescribed; R. laurentiana Lyster, 1940 is considered to be identical with the latter. A new species, R. milleri, is described. A host list and the geographical distribution of the 33 species of Rhabdochona so far recorded are given.


Author(s):  
D. W. Minter

Abstract A description is provided for Nothorhytisma nahuelitae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: Tarspot disease of southern beech. The symptoms and life cycle seem remarkably similar to those of Rhytisma acerinum. No serious damage seems to be done to infected trees. Like many South American members of the genus, Nothofagus pumilio is a deciduous tree. Unless the fungus is systemic, therefore, it seems likely that its life-cycle begins with the colonization of young leaves by air-dispersed ascospores in spring. Nothing is known of the appearance of young colonies, but stromata form during the summer and are followed by the conidial state in late summer. Ascomata form during winter on the dead fallen leaves, ripening during spring. The speed of development, and the stages during ripening are not known, but it is possible that the variability observed in the anatomy of ascomata before ascus production - the presence or absence of the extra layer above the lower wall - may represent two different points in the ripening process. HOSTS: Nothofagus pumilio (dead fallen leaf, living leaf). GEOGRAPHICAL DISTRIBUTION: SOUTH AMERICA: Argentina, Chile. TRANSMISSION: Presumably by air-borne ascospores released in humid conditions. The internal anatomy of the ascoma, and particularly the presence of mucus around the paraphyses, and the complex tissues at the periphery of the hymenium indicate that ascomata are likely to be able to shut again after the initial opening if conditions become dry, with the dark covering layer providing protection from uv light and desiccation. The widely-exposed hymenium suggests that ascospores are released by violent discharge, and are air-dispersed, probably in wet weather, following an increase in pressure within the ascoma generally and the ascus in particular, as a result of water uptake by the mucus around the paraphyses. Being colourless, thin-walled and without an obvious mucous sheath, the ascospores probably have little protection from UV light and desiccation after leaving the ascus (SHERWOOD 1981), and so are probably short-lived. Conidia may be water-dispersed.


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