RESUMEN
A perennial ryegrass (Lolium perenne L.) lawn located at Castelar (Buenos Aires Province) showed disease symptoms during the summer of 2003. Chlorotic patches as much as 15 cm in diameter appeared on the lawn. Later, dead plants with white mycelia developing on the crown and surrounding soil occurred at the periphery of the rings. Plants showed leaf chlorosis and crown and root rot. No sclerotia developed on plant organs. Diseased plants were collected, washed with running tap water for 4 h, and disinfested in 5% NaOCl for 2 min. Pieces, 3 to 5 mm long from symptomatic leaves, crowns, and roots, were incubated on 2% potato dextrose agar (PDA) at 22 to 25°C with a 12-h light/dark cycle. Mycelia growing on the soil surface was transferred to PDA and incubated under the same conditions. After 3 to 4 days, white, conspicuous mycelia that produced sclerotia grew from diseased tissue pieces and soil mycelial samples. Sclerotia were nearly spherical, 1 to 2 mm in diameter, white but turning brown with age, and produced in large numbers over the entire colony surface. Primary hyphae showed clamp connections at the septa. A pathogenicity test was performed with 20 1-month-old plants of L. perenne grown in a 1:1 (v/v) mixture of sand and soil contained in 24- × 17- × 4-cm plastic trays. Seven-day-old fungal cultures grown on PDA were cut into 1- cm2 pieces and placed among the plants on the substrate. Each tray was inoculated with seven inoculum pieces. Five trays of plants were inoculated with the fungus, and plants in five trays that served as controls had only sterile pieces of PDA placed on the substrate. All plants were maintained at 25°C and watered frequently. First symptoms, consisting of chlorosis, were observed 4 days after inoculation. Of the plants, 34, 59, 60, 65, and 70% developed symptoms 6, 9, 14, 17, and 21 days after inoculation, respectively. Control plants remained healthy. The fungus was reisolated from diseased plants and identified as Sclerotium rolfsii Sacc. (teleomorph Athelia rolfsii (Curzi) C.C. Tu & Kimbr.) on the basis of morphological and cultural characteristics (3,4). The disease has been observed causing stalk rot on perennial ryegrass in the United States (1) and Australia (2). To our knowledge, this is the first report of S. rolfsii causing disease on L. perenne in Argentina. 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) D. F. Farr et al. Fungal Databases. Systematic Botany and Mycology Laboratory. Online publication. ARS, USDA, 2007. (3) J. E. M. Mordue. No. 410 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, UK, 1974. (4) Z. K. Punja and A. Damiani. Mycologia 88:694, 1996.
RESUMEN
Lolium perenne L. is commonly used alone or in association with blue-grass and fescues in sport fields, parks, and gardens. During 2003, symptoms of an unknown disease were observed on L. perenne turfgrass in western Buenos Aires. Initial symptoms were indefinite yellow and green dappled spots that extended downward from the leaf tip, turned brown and finally gray, causing leaf death. Segments of symptomatic leaf tissues were surface sterilized and placed on 2% potato dextrose agar in petri dishes. After 4 days at room temperature, blackish brown colonies developed with dark brown septate conidiophores. Conidia were 21 to 29 × 9 to 13 µm, 3-septa, curved at the third cell from the base that is longer and darker than the others. Cells at each end are subhyaline and intermediate cells are medium brown. These characteristics are consistent with Curvularia lunata (Wakker) Boedijng (1). Pathogenicity tests were performed in five plastic trays with substrate of natural soil and sand (1:1 [v/v]) where the turfgrass (L. perenne cv. El Cencerro) was seeded. Plants were inoculated by spraying a suspension of 2 × 106 conidia per ml of sterile distilled water. Controls were sprayed with sterile distilled water. The trays were covered with transparent plastic bags, sprayed periodically with water, and incubated at 25°C in a greenhouse for 20 days. The first symptoms were observed 3 days later. After 9 days, 24% of the grass surface area showed blight lesions. C. lunata was consistently reisolated from affected tissues. Control plants remained symptomless. To our knowledge, this is the first report of C. lunata affecting L. perenne in Argentina. Reference: (1) M. B. Ellis and I. A. S. Gibson Cochliobolus lunatus (conidial state: Curvularia lunata). Page 474 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1975.
RESUMEN
During the summer of 2000, circular, yellow-to-brown, blighted, 2- to 4-cm-diameter patches were observed on creeping bentgrass (Agrostis stolonifera) putting greens (cv. Pennlinks) maintained at a 4- to 5-mm height on a golf course in Pilar (Buenos Aires, Argentina). Symptomatic leaves had transverse chlorotic bands that sometimes extended to the tip with brown lesions inside the bands. A fungus was isolated from symptomatic tissue after surface sterilization with 2% bleach for 1 min and plating on 2% potato dextrose agar (PDA). The mycelium was fluffy and white. The culture turned olive to brown and developed black stromata on the lower side of the plate base after 2 weeks. Pathogenicity tests were performed on 2-month-old healthy plants of A. stolonifera (cv. Crenshaw) grown in sterilized sand. Recently cut, 14-mm-diameter plugs of A. stolonifera were placed in 22- × 17-cm plastic trays filled with a sterilized mixture of 50:50 soil/sand (vol/vol). Plants were maintained at a 7-mm height. Two sources of inoculum were prepared; one was cultured on PDA at 22 to 25°C for 10 days and the other was prepared by incubating in sterilized soil at room temperature for 14 days. Twenty pieces of 1-cm-diameter agar blocks containing mycelium were placed in each plug at the base of the plants. In the infested soil inoculation, 25 g of soil were distributed among the plants on the substrate surface. Control plants were treated with either sterile PDA pieces or noninfested soil. The trays were irrigated with sterilized distilled water, covered with polyethylene bags, and kept in a controlled environment chamber at 25°C with 12 h per day of fluorescent light for 30 days. Leaf chlorosis appeared 7 and 10 days after inoculation for the agar-plug and infested-soil methods, respectively. Leaf necrosis was observed at day 23. Controls remained asymptomatic. The inoculated fungus was reisolated from symptomatic leaf tissue. The pathogen was identified as Sclerotinia homoeocarpa (1,2). To our knowledge, this is the first report of Sclerotinia homoeocarpa causing dollar spot disease on Agrostis stolonifera in Argentina and the first report of a disease on golf courses in our country. References: (1) J. E. M. Mordue. Sclerotinia homoeocarpa. No. 618 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1979. (2) R. W. Smiley. Dollar Spot. Pages 14-16 in: Compendium of Turfgrass Diseases. The American Phytopathological Society, St. Paul, MN, 1983.
RESUMEN
PIP: The author examines the role migrants from Mexico to the United States continue to play in the development of the regions they leave behind. The effect of remittances on the public and private sectors in the states of Zacatecas and Michoacan is analyzed as an illustration.^ieng