819 resultados para Egtitus sinensis


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Estudou-se o efeito de diferentes volumes de calda no controle do ácaro-da-leprose, Brevipalpus phoenicis (Geijskes), na cultura de citros (Citrus sinensis), em dois ensaios de campo, instalados em 1992 e 1993. Os ensaios foram delineados em blocos casualizados. Utilizou-se do óxido de fenbutatina (Torque 500 SC) a 0,01, 0,02, 0,04 e 0,08% de i.a., aplicado à razão de 5, 10, 20 e 40 litros de calda por planta. Os ácaros foram contados previamente e após a aplicação, amostrando-se 10 frutos/planta. Efetuou-se a retirada dos ácaros, com máquina de varredura, e as contagens com auxílio de microscópio estereoscópico. Concluiu-se que o óxido de fenbutatina independentemente das concentrações e volumes de calda, apresentou alta eficiência no controle do ácaro da leprose com reduções no número de ácaros durante o período do ensaio que variaram de 88,2 a 100% até 63 dias da aplicação (ensaio 1) e 75,4 a 100% até 123 dias (ensaio 2). A eficiência dependeu mais do volume do que da concentração, uma vez que, quanto maior o volume da calda, maior a redução da população. Aplicação de 40 l da calda/planta causou reduções médias de 99,3% e 96,7%, independente da concentração.

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Iphiseiodes zuluagai Denmark & Muma (Acari: Phytoseiidae) é um ácaro predador comumente encontrado em plantas cítricas (Citrus spp.). Alimentado com pólen de mamoneira (Ricinus communis ) e a 25 ± 2°C, 70 ± 10% de UR e 14 horas de fotofase, a maioria das larvas eclodiu entre 12 e 24 horas. A duração do estágio de larva foi freqüentemente em torno de 24 horas, e a duração das fases de protoninfa e deutoninfa entre 24 e 48 horas. O ciclo de ovo a adulto durou 5 a 6 dias. A estimativa da capacidade inata de crescimento da população (r m) foi 0,122 fêmeas/ fêmea/ dia; a duração média de uma geração (T) 18,7 dias; a taxa líquida de reprodução (Ro) 9,82 fêmeas/ fêmea e a razão finita de aumento (1)1,13.

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A ocorrência das espécies de ácaros predadores pertencentes à família Phytoseiidae, em folhas de laranjeira `Valência' (Citrus sinensis Osbeck), foi avaliada durante três anos em Lavras (MG), através de levantamentos quinzenais. Iphiseiodes zuluagai Denmark & Muma e Euseius alatus DeLeon foram as espécies mais freqüentes, a primeira representando 66,2% dos ácaros coletados e a segunda 29,8%. Ambos os ácaros foram encontrados ao longo de todos os anos, sendo que I. zuluagai apresentou maior ocorrência entre abril e setembro (outono e inverno), período de temperaturas amenas e baixa precipitação pluvial. A espécie E. alatus, ao contrário, apresentou maior ocorrência entre outubro e fevereiro, que correspondeu a um período de temperaturas elevadas e alta precipitação pluvial. Outras espécies levantadas e respectivas porcentagens de ocorrência foram: Amblyseius compositus Denmark & Muma (2,6 %), Amblyseius herbicolus (Chant) (1,1 %) e Phytoseiulus macropilis (Banks) (0,3 %), sendo A. compositus a mais freqüente e as demais ocasionais.

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Adição de carvão ativado e giberelina no meio de cultura podem proporcionar melhores condições no desenvolvimento de embriões imaturos de citros. Objetivou-se avaliar o efeito de carvão ativado e GA3 (ácido giberélico) no cultivo de embriões imaturos provenientes do cruzamento entre laranjeira 'Pêra Rio' x tangerineira 'Poncã'. Após 118 dias da polinização, frutos imaturos, com 3 a 4 cm de diâmetro, foram coletados, suas sementes removidas e tratadas com álcool (70%) por cinco minutos, hipoclorito de sódio (2%) por 20 minutos e, posteriormente, lavadas três vezes em água destilada e autoclavada. em condições assépticas, os tegumentos das sementes foram separados, os embriões globulares excisados e inoculados em tubos de ensaio contendo 15 mL do meio MT, acrescido de carvão ativado (0; 0,5; 1; 1,5 e 2 g L-1) e GA3 (0; 0,01; 0,1; 1 e 10 mg L-1). Após a inoculação, os embriões permaneceram por 90 dias em sala de crescimento a 27+1ºC, fotoperíodo de 16 horas e irradiância de 32 mmol m-2 s-1. Maior comprimento da parte aérea foi obtido em meio MT, acrescido de 0,1 e 1 mg L-1 de GA3, combinado com 2 g L-1 de carvão ativado. Maior comprimento do sistema radicular, massa da matéria fresca e número de folhas de plântulas foram obtidos em meio MT, acrescido de 0,01 mg L-1 de GA3, na ausência de carvão ativado. A adição de carvão ativado influenciou na concentração de ácido giberélico acrescido no meio de cultura.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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Difficulties in reproducing the citrus variegated chlorosis (CVC) disease symptoms in expertmental plants have delayed implementation of studies to better understand the essential aspects of this important disease. In an extensive Study, cultivars of sweet orange (Citrus sinensis) were inoculated with Xylella fastidiosa using procedures that included root immersion, and stein absorption, pricking, or infiltration of the inoculum into plants of different ages. Inoculum consisted of 5-day-old cultures or cell suspensions of CVC strain 9a5c diluted in phosphate-buffered saline. Inoculated plants and controls were grown, or transferred just after inoculation, to 5-liter pots or 72-cell foam trays. Approximately 4, 5, 9, and 12 months after inoculation, leaves were collected and processed for polymerase chain reaction analysis or X. fastidiosa isolation on BCYE agar medium. Root immersion and stem inoculation of 4- and 6-month-old plants resulted in low percentages of symptomatic (0 to 7%) and plants positive by isolation (0 to 9%). Pinpricked or injected stems of I-month-old seedlings resulted in high percentages of plants symptomatic (29 and 90% in Pera Rio, 75, 59, and 83% in Valencia, and 77% in Natal) or positive by isolation (26 and 93% in Pera Rio, 98, 96, and 83% in Valencia, and 77% in Natal), In foam trays, the seedlings grew less, the incubation period was shorter. and disease severity was higher than in pots. This system allows testing of higher numbers of plants in a reduced space with a more precise reproduction of the experimental conditions.

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Strains of Xylella fastidiosa, isolated from sweet orange trees (Citrus sinensis) and coffee trees (Coffea arabica) with symptoms of citrus variegated chlorosis and Requeima do Cafe, respectively, were indistinguish able based on repetitive extragenic palindromic polymerase chain reaction (PCR) and enterobacterial repetitive intergenic consensus PCR assays. These strains were also indistinguishable with a previously described PCR assay that distinguished the citrus strains from all other strains of Xylella fastidiosa. Because we were not able to document any genomic diversity in our collection of Xylella fastidiosa strains isolated from diseased citrus, the observed gradient of increasing disease severity from southern to northern regions of São Paulo State is unlikely due to the presence of significantly different strains of the pathogen in the different regions. When comparisons were made to reference strains of Xylella fastidiosa isolated from other hosts using these methods, four groups were consistently identified consistent with the hosts and regions from which the strains originated: citrus and coffee, grapevine and almond, mulberry, and elm, plum, and oak. Independent results from random amplified polymorphic DNA (RAPD) PCR assays were also consistent with these results; however, two of the primers tested in RAPD-PCR were able to distinguish the coffee and citrus strains. Sequence comparisons of a PCR product amplified from all strains of Xylella fastidiosa confirmed the presence of a CfoI polymorphism that can be used to distinguish the citrus strains from all others. The ability to distinguish Xylella fastidiosa strains from citrus and coffee with a PCR-based assay will be useful in epidemiological and etiological studies of this pathogen.

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Most of the cultivated species of citrus have narrow genetic basis. Relationships among species and cultivars are obscured by sexual compatibility, polyembryony, apomixis and a high incidence of somatic mutations. DNA analysis is crucial in genetic studies not only for citrus breeding programs but also for characterization of hybrids and species. In this paper, single nucleotide polymorphisms ( SNPs) were investigated in 58 accessions of Citrus, hybrids and related genera. Genomic sequences of 'Pera IAC' sweet orange ( Citrus sinensis L. Osbeck) were used for primer design and selection of sequence tagged sites (STSs) for identification of SNPs. Analysis of 36 STSs showed identical sequences among 40 of the 41 sweet orange accessions studied. However, these accessions were heterozygous for many SNPs. Ten selected STSs were analyzed in 17 additional accessions from 13 species and hybrids. Comparing to the 'Pera IAC' sweet orange accession, a total of 150 polymorphic nucleotides were identified and most of the alterations were transitions ( 52.7%). The greatest number of SNPs was observed in Poncirus trifoliata ( L.) Raf. and the smallest in 'Ponkan' mandarin ( Citrus reticulata Blanco). At the intra-specific level, 'Bafa Gigante' ( Citrus sinensis L. Osbeck) was the only sweet orange accession with a divergent SNPs genotype, which corroborates the hypothesis of a hybrid origin for this accession. Although the STSs analyzed represent randomly sampled genomic sequences, they provided consistent information about the level of polymorphism and showed the potential of SNPs markers for characterization and phylogenetic studies.

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The present study showed a strong deleterious effect on leaf-cutting ant Atta sexdens rubiopilosa nests supplied exclusively with sesame (Sesamum indicum) leaves in the laboratory. Sesame leaves were initially attractive to workers and later became antifeedant. Eucaliptus alba and Hibiscus rosa-sinensis leaves were used as control.

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Asiatic citrus canker, caused by Xanthomonas smithii ssp. citri, formerly X. axonopodis pv. citri, is one of the most serious phytosanitary problems in Brazilian citrus crops. Experiments were conducted under controlled conditions to assess the influence of temperature and leaf wetness duration on infection and subsequent symptom development of citrus canker in sweet orange cvs Hamlin, Natal, Pera and Valencia. The quantified variables were incubation period, disease incidence, disease severity, mean lesion density and mean lesion size at temperatures of 12, 15, 20, 25, 30, 35, 40 and 42 degrees C, and leaf wetness durations of 0, 4, 8, 12, 16, 20 and 24 h. Symptoms did not develop at 42 degrees C. A generalized beta function showed a good fit to the temperature data, severity being highest in the range 30-35 degrees C. The relationship between citrus canker severity and leaf wetness duration was explained by a monomolecular model, with the greatest severity occurring at 24 h of leaf wetness, with 4 h of wetness being the minimum duration sufficient to cause 100% incidence at optimal temperatures of 25-35 degrees C. Mean lesion density behaved similarly to disease severity in relation to temperature variation and leaf wetness duration. A combined monomolecular-beta generalized model fitted disease severity, mean lesion density or lesion size as a function of both temperature and duration of leaf wetness. The estimated minimum and maximum temperatures for the occurrence of disease were 12 degrees C and 40 degrees C, respectively.

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The objective of this work was to evaluate the mycelial growth of the Coprinus comatus strain CCO 01/01 in culture based on organic residues of Saccharum officinarum (sugarcane bagasse), Citrus sinensis (orange bagasse), Ananas comosus (pineapple residues) and Musa sp. (banana leaf), supplemented with wheat bran in the proportions of 0, 10 and 20%, kept at 27 degrees C. The mycelial growth of C. comatus was evaluated daily by measurement of the diameter of the colony during seven days of incubation. The banana leaf was considered the best residue for the cultivation of the C. comatus even without supplementation, meaning lower production costs. The supplementation of pineapple residues with 10% of wheat bran favored fungi growth. Sugar-cane bagasse was suitable for the growth of the C. comatus provided it is enriched with wheat bran. The orange bagasse, without pH correction, was not appropriate for the mycelial growth of C. comatus.

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)