Resumen de Controle biológico da mosca-do-mediterrâneo ceratitis capitata utilizando nematoides entomopatogênicos em laboratório

Ramon Santos de Minas, Claudia Dolinski, Rômulo da Silva Carvalho, Ricardo Moreira de Souza

• English

  The present study investigated under laboratory conditions the use of entomopathogenic nematodes strains separately or in combinations, as biological control agent of Mediterranean fruit fly, Ceratitis capitata Wied. (Diptera, Tephritidae). In the first bioassay, eight strains were used separately (Steinernema carpocapsae NCALL, Heterorhabditis bacteriophora HP88, H. baujardi LPP7, H. indica LPP1, H. indica LPP14, H. sp. LPP9, H. sp. LPP17 e H. sp. LPP12). For each treatment, 20 test tubes with sand, 10 larvae of C. capitata and 100 infective juveniles (IJs) diluted in 1 cm3 of distilled water were used. In the treatment control only 1 cm3 of distilled water was added. In the second bioassay it was used the same material; however, the number of C. capitata larvae was reduced to five and strains of nematodes combined in pairs, in a total of 100 IJs per replicate (50 individuals of each strain). All treatments were stored in an incubator for 15 days (28 ºC, 80% RU and 12 h photoperiod). The average mortality of larvae L3 was evaluated by Tukey test at 1%. The strains H. baujardi LPP7, H. indica LPP14, H. sp. LPP17 and H. sp. LPP12 were the most efficient ones, reaching mortalities range between 75 and 98.5%. In the second experiment, the most effective combinations were H. indica LPP14 + H. sp. LPP9 and H. sp. LPP17 + H. sp. LPP12 with mortality of 60 and 82%, respectively. We concluded that the use of NEPs in the biological control of C. capitata is a feasible alternative either using species separated or in combination, but the first one may reach higher mortality.

• português

  O presente trabalho avaliou em laboratório, a utilização de diferentes linhagens de nematoides entomopatogênicos (NEPs) individualmente e combinadas visando ao controle biológico da mosca-do-Mediterrâneo, Ceratitis capitata Wied. (Diptera, Tephritidae). No primeiro bioensaio foram utilizadas oito linhagens individualizadas de NEPs (Steinernema carpocapsae NCALL, Heterorhabditis bacteriophora HP88, H. baujardi LPP7, H. indica LPP1, H. indica LPP14, H. sp. LPP9, H. sp. LPP17 e H. sp. LPP12) sendo que para cada tratamento foram utilizados 20 tubos de ensaio cada um contendo areia,10 larvas L3 de C. capitata e 100 juvenis infectantes (JIs) diluídos em 1 cm3 de água destilada. No tratamento controle foi adicionado 1 cm3 de água destilada. No segundo bioensaio, foram utilizadas cinco larvas de C. capitata e as linhagens de nematoides foram combinadas duas a duas num total de 100 juvenis por repetição (50 JIs de cada linhagem) Os bioensaios foram conduzidos a 28 ºC, 80% UR e 12 de fotoperíodo. A mortalidade média das larvas foi avaliada pelo teste de Tukey a 1%. Individualmente as linhagens H. baujardi LPP7, H. indica LPP14, H. sp. LPP17 e H. sp. LPP12 foram as mais eficientes e causaram mortalidade entre 75 e 98,5%. As combinações mais eficientes foram H. indica LPP14 + H. sp. LPP9 e H. sp. LPP17 + H. sp. LPP12 com mortalidade de larvas L3 de 60 e 82%, respectivamente. Conclui-se que tanto separadamente ou em combinação, algumas linhagens de NEPs podem ser usadas no controle biológico de C. capitata, sendo que quando usadas separadamente, a eficiência é maior. ABSTRACT The present study investigated under laboratory conditions the use of entomopathogenic nematodes strains separately or in combinations, as biological control agent of Mediterranean fruit fly, Ceratitis capitata Wied. (Diptera, Tephritidae). In the first bioassay, eight strains were used separately (Steinernema carpocapsae NCALL, Heterorhabditis bacteriophora HP88, H. baujardi LPP7, H. indica LPP1, H. indica LPP14, H. sp. LPP9, H. sp. LPP17 e H. sp. LPP12). For each treatment, 20 test tubes with sand, 10 larvae of C. capitata and 100 infective juveniles (IJs) diluted in 1 cm3 of distilled water were used. In the treatment control only 1 cm3 of distilled water was added. In the second bioassay it was used the same material; however, the number of C. capitata larvae was reduced to five and strains of nematodes combined in pairs, in a total of 100 IJs per replicate (50 individuals of each strain). All treatments were stored in an incubator for 15 days (28 ºC, 80% RU and 12 h photoperiod). The average mortality of larvae L3 was evaluated by Tukey test at 1%. The strains H. baujardi LPP7, H. indica LPP14, H. sp. LPP17 and H. sp. LPP12 were the most efficient ones, reaching mortalities range between 75 and 98.5%. In the second experiment, the most effective combinations were H. indica LPP14 + H. sp. LPP9 and H. sp. LPP17 + H. sp. LPP12 with mortality of 60 and 82%, respectively. We concluded that the use of NEPs in the biological control of C. capitata is a feasible alternative either using species separated or in combination, but the first one may reach higher mortality.