The lesser date moth (LDM) Batrachedra amydraula is a significant pest of date palm fruits. Previously, detection and monitoring of the pest was inaccurate due to high costs of sampling with lifting machines. We report a practical system for detection and monitoring of LDM based on pheromone traps and relevant models. Dose-response experiments with LDM pheromone traps indicated a 1 mg lure is optimal for monitoring. Delta traps with adhesive covering their entire inner surface gave the highest captures while trap colour was unimportant. Sampling pheromone traps throughout the night indicated male flight began at 1:00-2:00 and reached a peak 2 h before sunrise. Monitoring traps exposed all year long in Israel revealed three generations with different abundance. Trapping transects in a date plantation indicated interference from a monitoring trap became minimal at distances >27 m away. Inter-trap distances closer than this may lower efficiency of monitoring and mass trapping in control programs. Our estimate of the circular effective attraction radius (EARc) of a 1 mg delta trap for LDM (3.43 m) shows this bait is among the most attractive compared with baits for other insects. We developed encounter-rate equations with the pheromone trap EARc to model the interplay between population levels, trap density and captures that are useful for detection of invasive LDM and its control by mass trapping. The integrated methodologies are applicable to many pest species.
The greater date moth (GDM), Aphomia sabella Hampson (Lepidoptera: Pyralidae: Galleriinae), is a serious pest of date palms, Phoenix dactylifera. The release of volatiles from both males and females was investigated using sequential SPME/GC/MS analysis. Males release a complex mixture of compounds in a circadian rhythm during the night between 03:00 and 05:00 hr. Six compounds were identified: benzaldehyde, sulcatol (6-methyl-5-hepten-2-ol), geranyl acetone [(E)-6,10-dimethyl-5,9-undecadien-2-one], phenylacetaldehyde, 2-phenylpropenal, and (R)-fuscumol [(R)-(E)-6, 10-dimethyl-5, 9-undecadien-2-ol]. Benzaldehyde, sulcatol, and geranyl acetone were found only in trace amounts. These compounds were in glands located in the forewing of males only. Small amounts of acetoin and 2,3-butanediol were found sporadically in the SPME/GC/MS analyses of volatiles from females, and these compounds probably originate from microorganisms. This is the first finding of a circadian release of male-specific compounds in moths. GC/EAD analyses with synthetic standards of compounds released by males showed that the female antenna is stimulated by all six compounds, while the male antenna responded only to phenylacetaldehyde. A possible pheromonal role for the male-specific compounds is suggested by the circadian rhythm of their release and the EAD response of females to them. However, trapping tests with the main male-specific compounds in screen cages in the laboratory or in the field did not reveal any significant behavioral responses from females or males. Copulation in the laboratory was observed only in the presence of date palm tissue, thus suggesting that sexual communication and mating of GDM moths probably occurs in the crown of date palms.
Animal species likely have different strengths of host habitat preference (HHP) that might be characterized by a standardized index ranging from 0 (no preference) to 1 (maximum preference). We hypothesized that in some species, HHP may result from individuals dispersing out of the host habitat having a probability of turning back at the boundary, or after entering host habitat by reducing speed or increasing size of turning angles. Computer simulations of individuals moving between various sized patches of host and nonhost habitat were conducted based on these three behaviours hypothesized to affect HHP. In the rebounding model, simulations resulted in equilibria of animal numbers inside and outside of host habitat that depend on sizes of these areas, initial number and the rebounding probability. Curvilinear regression of simulation results suggested an equation that predicted numbers in the host habitat and was solved for rebounding probability. A modified equation that sampled population densities (e.g., insect pheromone trap catches) inside and outside host habitat areas gave the rebounding probability, an index of HHP, without requiring the sizes of the areas. Simulations with traps and moving animals verified that the modified equation could predict the index correctly. The modified equation also estimates an index of HHP from sampled densities due to speed reductions and a combination of this and rebounding. Changes in angular turning size upon entering host habitat, however, did not affect habitat preference. Using pheromone trap captures, we found that the lesser date moth Batrachedra amydraula has a HHP for date Phoenix dactylifera plantations of 0.96. Host habitat preference indexes also were calculated from sampled insect densities reported in the literature. The new index of HHP is useful to characterize habitat patches of many organisms and aid understanding of animal spatial distributions and speciation processes. In addition, the index can be applied in studies of invasive species, trap crops of pest insects and conservation management.
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