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Title
Susceptibility of Polyphylla olivieri and Xanthogaleruca luteola to an entomopathogenic nematode, Heterorhabditis bacteriophora
Type of Research Presentation
Keywords
Bioassay, Elm, Infective juvenile, Landscape pests.
Abstract
White grubs and Elm leaf beetle are two economically important major pests of landscapes and parks in the most cities of Iran. These pests detrimentally affect wide range of trees. Ecologists believe that establishing landscape and parks can be of advantage to the environment and provide conditions for healthier life. In such places chemical based control of pests is severely prohibited not only for environmental pollutions but also due to higher hazards and risks to human. Therefore replacing the pesticides with efficient environmentally friendly approaches has critical importance. White grubs are among the most destructive pests of landscapes and parks. Immature stages chew off the roots of plants. Depends on the host, white grub damage typically appears as stunted, wilted, discolored and death of plant. In the current study, two year old Polyphylla olivieri larvae were exposed to native isolate of an entomopathogenic nematode, Heterorhabditis bacteriophora in filter paper assay by which individual larva was subjected to 1 ml of two concentrations of infective juveniles (IJs) including 500 and 1000 IJs/ml. The experiment was run twice with four replications. Each replication included 10 individuals of white grub larvae. Mortality was recorded after 48 h at one day intervals for four days. Results revealed that larval mortality was non-significant between IJs concentrations. In filter paper assays recording mortalities at successive days were 40, 80, 80 and 100%, respectively. In another experiment, the elm leaf beetle, Xanthogaleruca luteola, was used in the experiments. Six day old larvae of elm leaf beetle were involved in leaf assay. Twenty four-well plates lined with 2 layers of filter paper were loaded with concentrations of 32.5, 65, 130, 260, 520 and 1040 IJs/L. Then individual larva were added to each well. One 24-well plate was considered as a replication. The LC50-values were calculated using probit analysis at 36, 48 and 72 hours of larval exposure to t
Researchers (First Researcher)، Naser Eivazian Kary (Second Researcher)، Davoud Mohammadi (Third Researcher)