Navegando por Autor "Lima, Eraldo R."

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Age and time related pheromone production in coffee leafminer Leucoptera coffeella Guérin-Méneville (Lepidoptera: Lyonetiidae)
(Sociedade Brasileira de Química, 2008) Lima, Eraldo R.; Vilea, Evaldo F.; Lucia, Terezinha M. C. Della; Ataíde, Lívia M. S.
This study was undertaken to access the pattern of sex pheromone production in glands of virgin females of Leucoptera coffeella as an indirect measure of the calling behavior. The major compound, 5,9-dimethylpentadecane (1) was extracted from pheromone glands of virgin females to be used in two experiments. The first one investigated the effect of the pheromone production time by females (extracts of 10 females with age of two days were carried out at 2-hour intervals). The other experiment evaluated the effect of female age on pheromone production (10 females with age ranged from 1 to 5 days after emergence class were used). Hexane extracts were made with 5 ng µL-1 of 5,9-dimethylheptadecane (2) as internal standard and analyzed by GC. Females had the highest amount of pheromone at the last four hours in the dark and the two first hours in the light period. One-day old females produced the highest amount of pheromone in the glands.
Method for maintenance of coffee leaves in vitro for mass rearing of Leucoptera coffeellum (Guérin-Méneville) (Lepidoptera: Lyonetiidae)
(Sociedade Entomológica do Brasil, 2000-04-12) Reis Jr., Ronaldo; Lima, Eraldo R.; Vilela, Evaldo F.; Barros, Raimundo S.
To accomplish systematic studies with coffee leafminer, it is necessary to establish a mass rearing system under artificial conditions. It is possible to rear this species, from egg to adult, under laboratory conditions, without using coffee seedlings but detached leaves maintained in vitro. Synthetic cytokinins are routinely used for maintenance of plant cell and plant tissues in vitro. Two plant growth regulators, benzyladenin and kinetin, in concentrations 10-6 and 10-7 M were used to mantain the leaves. Green leaves collected in the field were maintained in the solution to be tested. Distilled water served as control. The experiment lasted 30 days, a period longer than the necessary for the complete development of the insect. Both artificial cytokinines indeed increased the lifetime of the coffee leaves, maintaining them green and healthy. Leaves placed in the cages for oviposition were attractive to the insect, with significant number of eggs per leaf. In most cases, eggs resulted in individuals that completed the whole developmental cycle. Tests with regulator in different concentrations with healthy leaves showed efficiency. However, we believe that hormone concentrations to be used with mined leaves should be larger, because these when maintained at 10-7 M leaves did not present a satisfactory lifetime. Therefore, tests with mined leaves with different hormone concentrations should be made to find out the ideal concentration for leaf survival. In our laboratory we are successfully using 10-6 M benzyladenin for the maintenance of mined leaves.