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Paul J. Zambino

Artificially inoculated single-leaf cuttings and small plants consistently differentiated european black currant (Ribes nigrum L.) cultivars susceptible to white pine blister rust (WPBR; Cronartium ribicola J.C. Fisch.) from immune cultivars carrying the Cr resistance gene. Black currant cultivars Consort, Crusader, and Titania showed no signs of infection with any of 21 strains of WPBR, suggesting that strains able to overcome immunity conferred by the Cr resistance gene, if they exist, are uncommon in North America. However, in red currant (Ribes rubrum L.), two sources of material presumed to represent the immune cultivar Viking showed no resistance to infection. All rust strains infected and sporulated as if the cultivar were fully susceptible, casting doubt on the true identity of available sources of `Viking'.

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D.R. Bergdahl and H.B. Teillon

White pine blister rust (WPBR) (Cronartium ribicola J. C. Fischer) has been present in Vermont and other northeastern states since the early 1900s. The fungus is commonly observed on currants and gooseberries (Ribes L.) every year, but incidence varies on eastern white pine (Pinus strobus L.). Our general impression has been that Vermont has had a relatively low level of infection on eastern white pines; however, we recently found rust incidence in Christmas tree plantings in northern Vermont to range from 10 to 42% (average 20%) based on 721 trees surveyed. Also, in pole-sized stands in southern Vermont, incidence ranged from 12 to 46% (average 32%) and 76% of these trees had main stem infections. In the southern survey, 98% of wild ribes plants had varied amounts of both urediniospores and teliospores. These preliminary survey data suggest that incidence of WPBR may be more significant than previously thought and therefore, additional survey work is needed. We screened cultivars of Ribes for susceptibility to WPBR. Eighteen cultivars were inoculated in the field with a mass collection of aeciospores of C. ribicola. The percentages of leaf area infected ranged from 0 to 49 for the urediniospore stage and from 0 to 55 for teliospores. The gooseberry (Ribes uva-crispa L.) `Welcome' had the highest percentage of leaf area with urediniospores, while black currants (R. nigrum L.) `Coronet,' `Consort,' and `Crusader' had no visible infection. Presently, Vermont has no WPBR regulations. However, previous federal laws did restrict black currant cultivation. Little is known about the genetic diversity of WPBR or its potential for change. Caution must be used when considering any cultivation of Ribes for the purpose of producing fruit because our valued white pine resources could be negatively impacted.

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J.K. Pataky

In parts of central Mexico, galls of common smut, caused by Ustilago maydis (Syn = Ustilago zeae Ung.), on ears of corn (Zea mays L.) are an edible delicacy known as cuitlacoche. Preliminary studies were done to identify methods to increase formation of ear galls on sweet corn. Of 370 sweet corn hybrids evaluated in disease nurseries, 38 hybrids were identified for which incidence of ear galls exceeded 40% in 1987 or 1988 or exceeded 12% in 1990. Inoculation techniques for inducing ear galls were: 1) spraying sporidial suspensions between leaf sheaths and stalks at the sixth to eighth nodes; 2) injecting sporidial suspensions into the sixth to eighth internodes; 3) wounding leaf sheaths at the sixth to eighth nodes with sand, followed by spraying a sporidial suspension into wounds; and 4) wounding leaf sheaths at the sixth to eighth nodes with sand in which teliospores were mixed. Only the sporidial injection technique substantially increased the incidence of smut, but it increased the incidence of stalk, tassel, and leaf galls more than ear galls. Thus, additional research is needed to determine when and how to inoculate with U. maydis to induce the formation of ear galls necessary to commercially produce cuitlacoche and to screen for disease resistance.

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M.E. Valverde, P. Fallah Moghaddam, M.S. Zavala-Gallardo, J.K. Pataky, O. Paredes-Lopez, and W.L. Pedersen

Ear gall development was evaluated after inoculating sweet corn (Zea mays L.) hybrids with Ustilago maydis (DC) Corda by injecting sporidial suspensions into silk channels when silks had emerged ≈3 to 6 cm from ear shoots. Gall incidence was ≈35% in two inoculation trials. About 0.5% of the noninoculated control plants was infected. Gall weight increased ≈250% to 500% between 14 and 21 days after inoculation, reaching a maximum of ≈280 to 600 g. Gall tissue was nearly 100% black and had lost its spongy integrity 19 to 21 days after inoculation, when mycelial cells formed powdery teliospores. A 1- or 2-day harvest window during which huitlacoche yield and quality were optimized corresponded to the time at which 60% to 80% of the gall tissue was black. The optimal huitlacoche harvest time varied among hybrids from 17 to 19 days after inoculation, but we suspect that optimal harvest time varies from ≈15 to 24 days after inoculation, depending on the growth stage at which the host is inoculated and the environmental conditions following inoculation. Differences among sweet corn hybrids in gall incidence, gall size, and coverage of mature galls by husk leaves were observed and could be used to select sweet corn hybrids that are well suited for producing huitlacoche.

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Michele R. Warmund, Jeanne D. Mihail, and Kaley Hensel

, teliospores, and basidiospores develop on Carex spp. ( Mims, 1981 ). At least 13 species of sedge have been reported as an alternate host for P. sambuci ( Afshan and Khalid, 2009 ; Arthur, 1962 ). Pycnia are the first signs observed on elderberry leaflets

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Jun Zeng, Jing Sun, Yang Xu, Fadi Chen, Jiafu Jiang, Weiming Fang, and Sumei Chen

). Under conditions of high humidity and mild temperature, its teliospores, which develop within a pustule on the abaxial leaf surface within 14 to 18 d post-infection ( Zandvoort et al., 1968b ), germinate to form a promycelium. Each promycelium bears a

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Jerald K. Pataky and Paul M. Richter

conditions (i.e., presumably wind and rain) that promote sporulation and dissemination of U. maydis teliospores and sporidia. Thus, reactions that appear to be associated with resistant or susceptible phenotypes based on natural infection may be the result

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Ebrahiem M. Babiker, Stephen J. Stringer, Barbara J. Smith, and Hamidou F. Sakhanokho

significant difference at P ≤ 0.05. Results Light and SEM. Light microscopy showed that the urediniospores were obovate with an echinulate wall and measured 17.1–27.2 × 12.3–17.3 µm ( Fig. 1 ). No teliospores were detected on the examined samples. FE