Barnard, E. L., EI-Gholl, N. E., and Gilly, S. P. 1988. Comparative spore morphology and pathogenicity of four Florida isolates of Nectria galligena. Plant Disease 72.973-976. Perithecia of Nectria ga//igena were observed in the field in association with I) stem galls on Cercis canadensis, 2) hypertrophied, roughened, and fissured bark in branch axils of Swietenia mahagoni, and 3) stem cankers on Quercus laurifolia and Acer rubrum. In the greenhouse, canker symptoms developed on seedlings of all four hosts in response to artificial wound inoculations with mass isolates from each host. Symptoms produced on S. mahagoni by the S. mahagoni isolate, however, were notably restricted in comparison with those produced on the other three hosts. Observations and measurements performed on ascospores, as well as on conidia of the Cylindrocarpon heteronema anamorph, revealed no distinct differences in spore sizes or septation patterns among isolates. C. canadensis, S. mahagpni, and, possibly, Q. laurifolia represent new host and suscept records for N. galligena. macfoconidia from these cultures, were observed and measured under oil immersion at XI,OOO. In addition, subcultures of each isolate were forwarded to C. Booth at the C.A.B. International Mycological Institute, Kew, Surrey, England for verification. Artificial inoculations and evaluation of pathogenicity. First-year seedlings of the four source host species with stem diameters of 0.5-1.0 cm were used for Nectria cankers are common and widespread on hardwood species in Europe, and N orth America, (2,7,8,13, 15,17). In Florida, we have observed perithecia typical of Nectria spp. in association with targetlike cankers on laurel oak (Quercus laurifolia Michx.) and red maple (Acer rubrum L.), as well as burl like galls on stems of eastern red bud (Cercis canadensis L.) (Fig. 1) and areas of hypertrophied, roughened, and fissured bark in branch axils of West Indies mahogany (Swietenia mahagoni Jacq.) (Fig. 2). In this paper we report results of studies to identify these fungi and to evaluate their pathogenicity on each of these hosts. A preliminary report has been published (3). cut with a cork borer from 2-wk-old PDA-plate subcultures. Each plug supported fungus mycelium and conidia of the Cylindrocarpon anamorph. Morphological comparison and identification of isolates. Perithecia of the Nectria teleomorph were induced on carnation leaf-water agar (12) after 3-4 wk in a growth chamber at 26.5 :t 0.5 C with alternating 12-hr lightl dark periods (approximately 3,000 Ix generated by GE F20TI21 CW fluorescent tubes). Ascospores, as well as microconidia and Fig. 2. Hypertrophied, roughened, and fissured bark in a branch axil of Swietenia mahagoni. MA TERIALS AND METHODS Isolation, culture maintenance, and inoculum preparation. Mass isolates (one per host) were obtained from ascospores exuded from Nectria perithecia removed from bark tissues collected from the four hosts (Fig. 3). Cultures were maintained at room temperature (25 ::!: 2 C) under normal laboratory lighting on potato-dextrose agar (PDA) (II). Inoculum for artificial inoculations consisted of 4-mm-diameter agar plugs
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