68 resultados para Benomyl
Resumo:
Objetivou-se estudar o efeito de diferentes concentrações de sacarose e benomyl na multiplicação in vitro de macieira (Malus prunifolia Willd, Borkh). O meio de cultura utilizado foi o MS, acrescido de 1 mg L-1 de BAP. O benomyl foi prejudicial à multiplicação da macieira em relação às variáveis estudadas. Concentrações de 30 a 45 g L-1 de sacarose propiciaram maior número de brotações e número de gemas. O comprimento dos brotos foi favorecido com 45 g L-1 de sacarose. As melhores respostas quanto à coloração das brotações foram obtidas com a adição de 15 a 30 g L-1 de sacarose.
Resumo:
Mudas das cultivares de abacaxi (Ananas comosus) 'Pérola' (suscetível) e 'Primavera' (resistente) foram inoculadas em casa de vegetação com isolados de Fusarium subglutinans f. sp ananas, resistentes e sensíveis ao benomyl, de diferentes áreas produtoras de abacaxi do Espírito Santo, visando estudar a virulência do patógeno. Foi utilizada suspensão de conídios obtidos pela raspagem da superfície das colônias desenvolvidas em meio BDA, cuja concentração final foi 10(5) conídios/ml. A inoculação de F. subglutinans f. sp ananas foi efetuada pela imersão de mudas injuriadas mecanicamente na base, com três meses de idade, na suspensão de inóculo. Dos 22 isolados testados preliminarmente, selecionou-se oito de F. subglutinans f. sp ananas, sendo quatro representativos do grupo dos sensíveis ao benomyl (E285, E277, E278 e E290) e quatro representativos do grupo dos resistentes ao benomyl (E272, E274, E279 e E283) para realização do teste final. Os resultados comprovaram a resistência da cv. Primavera a todos os isolados testados. Plantas da cv. Pérola apresentaram sintomas da doença aos 15 dias após a inoculação com isolados resistentes ao benomyl; os isolados sensíveis ao benomyl só foram capazes de causar sintomas severos da doença aos 45 e 60 dias após a inoculação. O isolado E272, resistente ao benomyl, foi o mais virulento, tendo causado a maior lesão e a morte das plantas aos 30 dias após a inoculação; os isolados E277 e E278 foram os mais virulentos. Houve diferenças em virulência de isolados de F. subglutinans f. sp. ananas resistentes e sensíveis ao benomyl ao abacaxizeiro.
Resumo:
The effectiveness of fungicides in controlling white mold (Sclerotinia sclerotiorum) of dry beans (Phaseolus vulgaris) was evaluated when they were applied through irrigation water directly onto the plants or only to the soil. Two field trials were installed in April 1998 and April 1999 in Viçosa, MG. Trials were conducted as a (2 x 3) + 1 factorial: two fungicides x three application modes + one untreated control. The fungicides were benomyl (1.0 kg a.i. ha-1) and fluazinam (0.5 l a.i. ha-1). The three application modes were: (a) by backpack sprayer (667 l ha-1), (b) by garden watering-cans simulating sprinkler irrigation with 35,000 l ha-1 of water, and (c) by garden watering-cans applying water between the rows and near the soil surface in 35,000 l ha-1 of water. In 1998, fungicides were applied at 43 and 54 days after emergence (DAE); in 1999, at 47 and 61 DAE. Both fungicides were similarly effective on white mold control when applied by either chemigation or backpack sprayer, resulting in yields 21% higher than untreated control. Only fluazinam provided disease control when applications were made only in soil. Chemigation provided white mold control equivalent to that of backpack sprayer in terms of incidence, severity and number of diseased pods. Consequently, yield differences between these application methods were not significant.
Resumo:
A simple High Performance Liquid Chromatograph (HPLC) method has been developed to identify benamyl (methyl 1- (butylcarbamoyl)-2-benzimidazole carbamate) and MBC (methyl 2-benzimidazole carbamat~ residues on apple leaves without cleanup. Sample leaves are freeze dried in a Mason jar and residues are then extracted by tumbling them in chloroform containing 5,000 microgram per milliliter of n-propyl isocyanate (PIC) at 10 C. To the extract, n-butyl isocyanate (BIC) was added at 5,000 microgram per milliliter and 20 microliter of this mixture injected onto the HPLC system. Separation is accomplished by the use of a Brownlee LiChrosorb silica gel column with a guard column and' operated with a mixed mobile phase consisting of chloroform and hexane (4:1) saturated with water. MBC, a degradation product of benomyl is identified if present as methyl l-(npropyl carbamoyl)-2-benzimidazole carbamate (MBC-n-PIC). Both benomyl and MBC-n-PIC can be detected with aKUltraviolet (UV) detector (280nm) at a concentration as low as 0.2 microgram per milliliter in apple leaves. The fate of benomyl on apple foliage after spray application of benomyl (Ben late 50 per cent wettable powder) was investigated by the method thus described. Benomyl quickly dissipated during the first 3-7 days, but the dissipatio'n sltowed down thereafter. In contrast, the concentration of MBC in leaves gradually increased after repeated applications of Benlate.
Resumo:
Two benomyl-resistant mutants, benD3 tubC41 and benD4 tubC42, of Aspergillus nidulans were isolated after UV treatment. The tubC mutations permitted good conidiation of these strains in culture media containing benomyl and were responsible for increasing their benomyl resistance levels. This implies that β3-tubulin, a product of the tubC gene, in addition to being involved in fungal conidiation, participates in the vegetative growth of the fungus. The tubC gene was located in linkage group I.
Resumo:
Postbloom fruit drop (PFD) of citrus caused by Colletotrichum acutatum produces orange-brown lesions on petals and induces the abscission of young fruitlets and the retention of the calyces. Despite the fact that C. acutatum is not highly sensitive to benomyl in culture, this fungicide provides good control of the disease under field conditions. This study was undertaken to determine the effect of benomyl on various stages of disease development to understand the basis for its effectiveness in the field. We found that benomyl at 1.0 μg/ml reduced colony area of C. acutatum by about 75% and completely inhibited growth of C. gloeosporioides. Benomyl did not prevent conidial germination even at 100 μg/ml, but reduced germ tube elongation at 10 and 100 μg/ml. When benomyl was applied to flower clusters on screen-house-grown plants before inoculation, disease severity was greatly reduced. Applications at 24 and 48 h, but not at 72 h, after inoculation reduced PFD severity. Application of benomyl to symptomatic petals not bearing conidia did not prevent or reduce production of inoculum. Application to petals bearing conidia reduced viability of these fungal propagules by only about 50%. The viability of appressoria on mature leaves was not affected by benomyl application. Even when appressoria on mature leaves were stimulated to germinate by treatment with flower extracts, subsequent application of benomyl did not reduce propagule numbers below original levels. Benomyl appears to act by preventing infection and early development of the fungus in petals. However, once symptoms have developed, this fungicide has only minimal effects on further disease development and spread.
Resumo:
Postbloom fruit drop (PFD) of citrus, caused by Colletotrichum acutatum, produces orange-brown lesions on petals and results in premature fruit drop and the retention of calyces. C. gloeosporioides is common in groves and causes postharvest anthracnose on fruit. Both diseases are controlled effectively by the fungicide benomyl in research fields and commercial orchards. Highly sensitive and resistant isolates of C. gloeosporioides were found, whereas all isolates of C. acutatum tested were moderately resistant. In preliminary studies conducted in vitro with three isolates of each, mycelial growth of sensitive isolates of C. gloeosporioides was inhibited completely by benomyl (Benlate 50 WP) at 1.0 μg/ml, whereas resistant isolates grew well at 10 μg/ml. Growth of all isolates of C. acutatum was inhibited by about 55% at 0.1 μg/ml and by 80% at 1.0 μg/ml. Spore germination of C. acutatum was inhibited more at 0.1 μg/ml than at 1.0 μg/ml or higher concentrations. In all, 20 isolates of C. acutatum from 17 groves and 20 isolates of C. gloeosporioides from 7 groves were collected from locations with different histories of benomyl usage in São Paulo, Brazil, and Florida, United States. Benomyl at 1.0 μ.g/ml completely inhibited growth of 133 isolates of C. gloeosporioides, with the exception of 7 isolates that were highly resistant to the fungicide, whereas all isolates of C. acutatum were only partially inhibited at 0.1 and 1.0 μg/ml. Analysis of variance indicated that the sensitivity of the isolates of C. acutatum was not affected by benomyl usage or grove of origin, and country of origin had only minor effects. No highly resistant or sensitive isolate of C. acutatum was recovered. Partial sequencing of the β-tubulin gene did not reveal nucleotide substitutions in codons 198 or 200 in C. acutatum that usually are associated with benomyl resistance in other fungi.
Resumo:
In biopulping, efficient wood colonization by a selected white-rot fungus depends on previous wood chip decontamination to avoid the growth of primary molds. Although simple to perform in the laboratory, in large-scale biopulping trials, complete wood decontamination is difficult to achieve. Furthermore, the use of fungal growth promoters such as corn steep liquor enhances the risk of culture contamination. This paper evaluates the ability of the biopulping fungus Ceriporiopsis subvermispora to compete with indigenous fungi in cultures of fresh or poorly decontaminated Eucalyptus grandis wood chips. While cultures containing autoclaved wood chips were completely free of contaminants, primary molds grew rapidly when non-autoclaved wood chips were used, resulting in heavily contaminated cultures, regardless of the C. subvermispora inoculum/wood ratio evaluated (5, 50 and 3000 mg mycelium kg(-1) wood). Studies on benomyl-amended medium suggested that the fungi involved competed by consumption of the easily available nutrient sources, with C. subvermispora less successful than the contaminant fungi. The use of acid-washed wood chips decreased the level of such contaminant fungi, but production of manganese peroxidase and xylanases was also decreased under these conditions. Nevertheless, chemithermomechanical pulping of acid-washed samples biotreated under non-aseptic conditions gave similar fibrillation improvements compared to samples subjected to the standard biodegradation process using autoclaved wood chips.
Resumo:
Nutrition in bean plants and anthracnose intensity in function of silicon and copper application. The objective of this work was to evaluate the effect of calcium silicate and copper sulfate on anthracnose intensity and nutrition of bean plants. The experiment was conducted using an experimental design in randomized blocks following a 4 x 4 factorial arrangement , (four levels of calcium silicate and four levels of copper sulfate) and two additional treatments (plants without inoculation and plants sprinkled with Benomyl). Four evaluations of the incidence and severity of anthracnose were done, in addition to measuring, total leaf area. At the end of the evaluations, incidence: and data were integrated over time, obtaining the area under disease progress curve (AUDPC). Contents of N, P, K, Ca, Mg, B, Cu, Fe, Mn, Zn, Si and lignin were determined in the aerial Part. A linear decrease of the intensity AUDPC was observed with the increase of the doses of calcium silicate. The severity AUDPC was influenced by the doses of copper, obtaining a reduction of 35% on the higher dosage. The supply of silicon and copper altered the content of the K, mg, S, Zn, Ca and Si in the aerial part of the bean plants.
Resumo:
The in vitro efficacy of several fungicides against Botryosphaeria dothidea (syn. Dothiorella dominicana) and their in vivo efficacy in controlling mango cv. Kensington Pride stem-end rot on partial-pressure infiltration v. dip treatment of green mature fruit was evaluated. In vitro sensitivity of B. dothidea to Benlate (benomyl), Sportak (prochloraz) and Scala (pyrimethanil) at 10 dilutions of the manufacturer's recommended rate was first determined at typical cold (13degreesC) and shelf (23degreesC) storage temperatures. The effectiveness of partial-pressure infiltration and conventional hot (52degreesC) or cold (26degreesC) dipping of fruit after harvest was then evaluated using the commercially recommended rate for each fungicide. In vitro, Benlate and Sportak prevented the growth of B. dothidea at both storage temperatures and at all concentrations, while Scala partially controlled growth of the pathogen. Benlate was the most effective fungicide for stem-end rot control. Sportak and Scala resulted in stem-end rot control when applied by partial-pressure infiltration, but not as dips. Partial-pressure infiltration holds promise for enhancing the efficacy of otherwise less effective but alternative fungicides for control of stem-end rot diseases.
Resumo:
Neste trabalho, objetivou-se a caracterização de uma enfermidade ainda nova para o Estado do Acre, na castanha-do-brasil (Bertholletia. excelsa), onde, após, exames macro e microscópios, foi constatado que tal doença era causada pelo fungo do gênero Colletotrichumsp. Em pesquisas de laboratório, foi testada a eficiência de quatro produtos químicos: MONCOZEB, BENOMYL, TIABENDAZOLE e PCNB, na inibição do desenvolvimento micelial "in vitro" do fungo Colletotrichumsp. Os resultados indicaram que apenas o Moncozeb não apresentou efeito inibidor sobre o crescimento do fungo. Os demais inibiram totalmente o crescimento micelial do fungo estudado.
Resumo:
Foram realizadas avaliações biométricas em frutos e sementes de Parkia nitida e estudado o efeito dos tratamentos escarificação mecânica sem (T2) e com (T3) aplicação do fungicida Benomyl; imersão em Η2Ο a 80°C (T4) e a 100°C (T5); imersão em H2SO4 durante 10 (T6), 20 (T7), 40 (T8) e 80 (T9) minutos, na superação da dormência das sementes. Foram totalizadas as sementes germinadas aos 10, 20, 30 e 40 dias após a semeadura. O ensaio foi instalado com quatro repetições de 50 sementes, semeadas em substrato de vermiculita. O número de frutos/inflorescência variou de um a oito. O comprimento e largura dos frutos e o número de sementes/fruto variaram de 36,0 a 80,0 cm, de 4,6 a 6,5 cm e de 17 a 37 sementes, respectivamente. O comprimento, a largura e a espessura das sementes variaram de 16,1 a 24,0 mm, de 8,1 a 14,0 mm e de 5,1 a 9,0 mm, respectivamente. Houve interação significativa entre métodos para superação da dormência e dias decorridos após a semeadura na germinação das sementes. As análises de regressão mostraram significância para os tratamentos T2, T3, T4, T6 e T8. O T4 proporcionou apenas 10,0% de germinação; entretanto os tratamentos T2 e T3 tiveram efeito satisfatório, com 50,0% e 72,5% de germinação, respectivamente. Os tratamentos com H2SO4 estiveram entre os mais eficientes, com 80,0%, 82,5%, 80,5% e 74,5%, durante 10, 20, 40 e 80 minutos de imersão, respectivamente. As percentagens de germinação para o T1 (testemunha) e T5 foram inferiores a 2,5%. Concluiu-se que sementes de P. nitida apresentam dormência devido à impermeabilidade do tegumento à água; é necessária a escarificação das sementes para se obter elevada percentagem de germinação; tratamentos com H2SO4, por 20 minutos, e escarificação mecânica + fungicida constituem-se métodos eficientes para superação da dormência.
Resumo:
O objetivo deste trabalho foi estabelecer um protocolo para a regeneração in vitro de pau-rosa (Aniba rosaeodora Ducke), utilizando brotações apicais e segmentos nodais inoculados em meio de cultura com distintas concentrações de diferentes reguladores de crescimento. Explantes esterilizados com soluções de benomyl (4,0 g.L-1) por 24 horas e hipoclorito de sódio a 20% + tween 20 por 20 minutos, foram submetidos a um experimento de indução de broto, raiz e calo em meio MS1 acrescido de 30g.L-1 de sacarose e 9g.L-1 de agar, suplementado com BAP (0,0 e 4,0 mg.L-1), ANA, AIA e 2,4-D (0,0; 3,0 e 6,0 mg.L-1), e suas respectivas combinações. O delineamento utilizado foi o inteiramente casualizado em esquema fatorial 7 X 2, com 14 tratamentos e 15 repetições cada, onde foram analisados o número médio de brotos, raízes e calo. Após 90 dias, os resultados mostraram que a presença de auxinas é fundamental para a formação dos parâmetros induzidos nos explantes de pau-rosa. O meio de cultura contendo 4,0 mg.L-1 de BAP + 6,0 mg.L-1 de AIA apresentou a melhor média para a brotação com 2,13 brotos/explante. Para o enraizamento o meio contendo 3,0 mg.L-1 de ANA foi o mais eficiente, apresentando uma média de 2,53 raízes/explante. Em relação à indução de calo, todos os tratamentos apresentaram calogênese, porém o meio suplementado com 4,0 mg.L-1 de BAP + 6,0 mg.L-1 de 2,4-D, apresentou a melhor média, 1,67 calos/explante.
Resumo:
Mangas 'Bourbon' foram conservadas em câmara fria, a temperatura de 10º C, tendo recebido previamente os seguintes tratamentos em pós-colheita: 1) controle; 2) imersão por 10' em água a 55 C; 3) imersão por 5' a 50 C em solução de Benomyl a 0,025% de p.a.; 4) imersão por 5' a 50ºC em solução de Benomyl a 0,050%; 5) imersão por 5' a 55ºC em solução de Benomyl a 0,025% de p.a. e 6) imersão por 5' a 55ºC em solução de Benomyl a 0,050% de p.a. Os resultados indicaram que todos os tratamentos, com exceção do controle, foram eficientes no controle da antracnose. Quanto à ocorrência das podridões moles, constatou-se perdas de 44, 36, 20, 20, 4 e 8% do primeiro para o sexto tratamento, respectivamente. Assim ficou evidenciado que os tratamentos à mais alta temperatura, conjugados ao fungicida Benomyl, foram aqueles mais interessantes no tratamento em pós-colheita de manga 'Bourbon' .