With the objective of determining the effects of initial infection level (% leaf area infected, % l.a.i.) at the time of fungicide and foliar nutrient application for the control of powdery mildew, a study was carried out under greenhouse conditions at Embrapa Soja, Londrina, P.R. The fungicide tebuconazole (100 g a.i./ ha/application) and sulphur fungicide (2.0 kg a.i./ha/ application), sprayed at 20, 30, 40 and 50% l.a.i. (growth stages V3 and V5, between R5.1 and R5.3), and three applications (at V3, V4 and R5.1, beginning at 20% l.a.i.) of tebuconazole were compared with sulphur foliar nutrient (sulphur at the dose of 125 g a.i./ha/ application). The highly susceptible BR-16 cultivar was used in a completely randomized design with 11 treatments, five replications (pots) and five plants per pot. The parameters evaluated were: % l.a.i., % yellowing leaf when the control reached growth stage R7.2 (between 50 and 75% yellow/mature leaves), % defoliation (% defol.) when the control plants reached R8.2 (pre-harvest maturity), number of pods and seeds and seed weight (s.w.) per plant. The area under the disease progress curve (AUDPC) was determined based on disease progress. The % l.a.i. and AUDPC of the control (98% and 65.41) differed from other treatments (3.5-64.2% l.a.i. and 13.57-40.59 AUDPC). The % l.a.i. for the sulphur fungicide treatment (41.9-64.2%) and sulphur foliar nutrient (49.8%) were greater than for tebuconazole (3.5-28%). The % defol. of the control (90%) differed from tebuconazole applied at 30% initial infection (48%), with three applications (45%), and from sulphur foliar nutrient (47%). The s.w./plant of the control (2.23 g) was lower than that of tebuconazole treated at 40% IL (3.03 g) and at 20% IL (3.35 g) and for sulphur foliar nutrient (3.7 g). The initial disease severity (20-50% l.a.i.) did not affect the level of powdery mildew control and the sulphur foliar fertilizer resulted in greater number and higher s.w./plant.
A bactéria Xylella fastidiosa possui uma ampla gama de plantas hospedeiras que inclui espécies de pelo menos 28 famílias de mono e dicotiledôneas. Em cafeeiro (Coffea spp.), a ocorrência dessa bactéria foi relatada previamente em cultivares da espécie Coffea arabica. Estudos foram realizados para determinar a presença de X. fastidiosa em diferentes espécies e híbridos interespecíficos de cafeeiro. As amostragens foram realizadas em dois anos consecutivos. As espécies de cafeeiro examinadas foram: C. kapakata, C. canephora, C. racemosa, C. arabica, C. dewevrei, C. stenophylla e C. eugenioides. Também foram incluídos neste estudo híbridos interespecíficos de C. arabica: C. arabica x C. dewevrei, C. arabica x C. eugenioides, C. arabica x C. racemosa e C. arabica x C. robusta. Foram coletadas amostras de ramos plagiotrópicos de diferentes plantas para cada espécie e híbrido. A detecção de X. fastidiosa nas amostras foi realizada utilizando os testes serológicos de DAS-ELISA e imunofluorescência indireta. A bactéria foi detectada nas sete espécies e nos quatro híbridos de cafeeiro examinados. Entretanto, as plantas aparentemente não apresentavam sintomas de infecção por X. fastidiosa. A espécie C. arabica apresentou a maior proporção de amostras positivas e maiores valores de absorbância no teste de DAS-ELISA. Em contraste, as espécies C. racemosa e C. dewevrei foram as que apresentaram menores proporções de amostras positivas para presença de X. fastidiosa, como também menores valores de absorbância no teste de DAS-ELISA.
In 1998, plants of periwinkle (Catharanthus roseus L.) showing small leaves, short internodes, and dieback symptoms were observed in a garden at the Instituto Agronomico do Parana (IAPAR), Londrina, PR, Brazil. Stems of these plants were cut into short sections and the sap extracted from the tissue by squeezing with pliers. The sap was blotted onto a glass slide and examined for the presence of bacteria by light microscopy (×400). Microscopy observations revealed the presence of a large number of slender, rod-shaped bacterial cells. The bacteria present in the stems of periwinkle were isolated on buffered cysteine-yeast extract (BCYE) and periwinkle wilt (PW) agar media. Stems were disinfected in 70% alcohol and cut into short sections, and the sap extracted as described above. The sap was blotted directly onto the media and the plates were incubated at 28°C. Typical colonies of Xylella fastidiosa were observed 10 days after isolation on both media. Indirect immunofluorescence tests with antibody specific to X. fastidiosa and anti-IgG conjugated with tetrametylrhodamine isothiocyanate (TRITC) were carried out with xylem sap of periwinkle stem and the isolated bacteria. In both cases, immunofluorescence tests were positive for X. fastidiosa. These results confirm that periwinkle plants were infected with X. fastidiosa. This is the first report of the association of X. fastidiosa with periwinkle plants in Brazil. However, the symptoms observed for the X. fastidiosa-infected periwinkle plants differed from those described previously in the U.S. (1): those symptoms consisted of marginal chlorosis and occasional vein clearing of leaves and wilting of the plants. Reference: (1) R. E. McCoy et al. Plant Dis. Rep. 62:1022, 1978.
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