Willian Bucker Moraes

Prof. Dr. Willian Bucker Moraes

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 April 2020 in Crop Protection
Verified
Journal Article
Closed access
LBLeonardo Leoni Belan
Leonardo Leoni Belan
ARAnatan da Matta Rafael
Anatan da Matta Rafael
CGCarlos Alberto Gonçalves Gomes
Carlos Alberto Gonçalves Gomes
FAFábio Ramos Alves
Fábio Ramos Alves
WJWALDIR CINTRA JESUS JUNIOR
WALDIR CINTRA JESUS JUNIOR
WMWillian Bucker Moraes
Willian Bucker Moraes

1 December 2008 in Scientia Agricola
Verified
Journal Article
Open access
PDF file
WJWALDIR CINTRA JESUS JUNIOR
WALDIR CINTRA JESUS JUNIOR
RJRanolfo Valadares Júnior
Ranolfo Valadares Júnior
Roberto Avelino CecílioRoberto Avelino Cecílio
Roberto Avelino Cecílio
WMWillian Bucker Moraes
Willian Bucker Moraes
FVFrancisco Xavier Ribeiro Do Vale
Francisco Xavier Ribeiro Do Vale
PPPierce Anderson Paul
Pierce Anderson Paul
As mudanças climáticas poderão alterar as doenças de plantas e afetar a eficácia das medidas de manejo. Um dos prováveis impactos será na distribuição geográfica das doenças. A Sigatoka Negra é considerada a principal doença da cultura da banana em decorrência dos danos causados e aumento do custo de manejo. O impacto sócio-econômico da doença continua aumentando, uma vez que a doença tem atingido novas áreas de plantio, tornando o manejo mais difícil. Este trabalho tem por objetivos comparar a distribuição geográfica da doença por meio da elaboração de mapas nas seguintes situações: a) clima atual e futuro (2020, 2050 e 2080), b) cenários A2 e B2 do Painel Intergovernamental de Mudanças Climáticas, c) predito por seis diferentes modelos de mudanças climáticas e pela média dos mesmos e, d) entre meses. Haverá redução das áreas favoráveis à doença no futuro, sendo que tal redução será mais acentuada no cenário A2 do que no B2 e gradativa para as décadas de 2020, 2050 e 2080. Predições efetuadas com o uso da média dos dados estimados pelos modelos permitiram redução na variabilidade da simulação em comparação com a predição gerada por cada modelo individualmente. Alterações na distribuição geográfica da doença ocorrerão entre meses, de modo que áreas consideradas desfavoráveis tornar-se-ão favoráveis e vice-versa. Apesar disso, extensas áreas continuarão favoráveis ao desenvolvimento da Sigatoka Negra.

11 January 2020 in European Journal of Plant Pathology
Verified
Journal Article
Closed access
PDF file
LBLeônidas Leoni Belan
Leônidas Leoni Belan
WJWaldir Cintra de Jesus Junior
Waldir Cintra de Jesus Junior
ASAntônio Fernando de Souza
Antônio Fernando de Souza
LZLaércio Zambolim
Laércio Zambolim
JFJoel Cardoso Filho
Joel Cardoso Filho
WMWillian Bucker Moraes
Willian Bucker Moraes

22 July 2016 in Forest Pathology
Verified
Journal Article
Closed access
PDF file
CAClayton Alvares
Clayton Alvares
PSP. C. Sentelhas
P. C. Sentelhas
EME. M. Mattos
E. M. Mattos
AMA. C. Miranda
A. C. Miranda
WMWillian Bucker Moraes
Willian Bucker Moraes
JSJ. L. Stape
J. L. Stape

1 March 2012 in Summa Phytopathologica
Verified
Journal Article
Open access
PDF file
LSLeonardo Nazário Silva dos Santos
Leonardo Nazário Silva dos Santos
FAFábio Ramos Alves
Fábio Ramos Alves
LBLeônidas Leoni Belan
Leônidas Leoni Belan
PCPablo Cabral
Pablo Cabral
FMFrederico de Pina Matta
Frederico de Pina Matta
WMWillian Bucker Moraes
Willian Bucker Moraes
The damage and the resistance levels of cultivars and accessions of common beans rescued in the South and mountain regions of Espírito Santo State, Brazil, to M. incognita race 3 and M. javanica parasitism were evaluated under a greenhouse. Four rescued bean genotypes ("FORT-10", "FORT-13", "FORT-16" and "FORT-19") and 2 commercial cultivars: "Pérola", and "Aporé", were tested. The cultivar "Rico-23" was included as standard of susceptibility to nematodes and non-inoculated plants constituted the control. Thus, the experiment was carried out in a completely randomized design in 3 (treatments considering nematodes) x 7 (genotypes and bean cultivars) factorial arrangement, with 7 replicates. Data were measured at 50 days after plant inoculation. For damage quantification, the following variables were evaluated: plant height (PHE), number of nodes (NNO), number of trifoliate leaves (NRT), fresh matter weight (FWE) and dry matter weight (DWE) of shoots, root weight (RWE), number of root nodules (NRO) and final population (FPO) of nematodes per root system. There were no significant differences between the effects caused by M. incognita and M. javanica, but both species showed inferior values of PHE, NNO, NRT, RWE, FWE and DWE compared to controls. Concerning the levels of resistance of bean plants to M. incognita, the genotypes "FORT-10", "FORT-13", "Aporé" and "FORT-16" behaved as moderately resistant, the cultivars "Rico 23" and "Pérola" low resistant, and the genotype "FORT-19" as highly susceptible. When parasitized by M. javanica, the beans "FORT-19", "Rico-23", "FORT-16" and "FORT-13" were low resistant, "Pérola" and "Aporé" susceptible and "FORT-10" highly susceptible.

1 September 2018 in Plant Disease
Verified
Journal Article
Open access
LBL. L. Belan
L. L. Belan
ARAnatan Matta Rafael
Anatan Matta Rafael
RLRodrigo Monte Lorenzoni
Rodrigo Monte Lorenzoni
FSF. B. Souza-Sobreira
F. B. Souza-Sobreira
TSTais Cristina Bastos Soares
Tais Cristina Bastos Soares
WMWillian Bucker Moraes
Willian Bucker Moraes
Coffea canephora plants have been wilting and dying in major producing regions of Brazil; however, the disease etiology is unknown. Coffee clones differ in susceptibility, and disease occurs throughout the year. The symptoms include wilting, leaf yellowing, defoliation, vascular tissue darkening, and drying and death of plagiotropic and orthotropic branches and the plant. To identify the etiological agent, vascular tissue fragments from symptomatic plants collected in the Jerônimo Monteiro municipality (20°53′28′′S, 41°25′59′′W) were surface sterilized, placed on carrot baits, and incubated at 26 °C. The resulting mycelia were transferred to potato dextrose agar (PDA) medium and incubated at 26 °C, in 12 h light/dark for 10 days. Monosporic cultures from four isolates were prepared and characterized (Booth, 1971; Summerell et al., 2013). A TEF-1α gene fragment was amplified (O’Donnell et al., 2000). The PCR products were sequenced by capillary electrophoresis (ABI3730) using POP7 polymer and BigDye v3.1 (...