Efficacy of Two Entomopathogenic Fungi, Metarhizium brunneum, Strain F52 Alone and Combined with Paranosema locustae against the Migratory Grasshopper, Melanoplus sanguinipes, under Laboratory and Greenhouse Conditions.

Grasshopper outbreaks cause significant damage to crops and grasslands in US. Chemical control is widely used to suppress these pests but it reduces environmental quality. Biological control of insect pests is an alternative way to reduce the use of chemical insecticides. In this context, two entomopathogenic fungi, Metarhizium brunneum strain F52 and Paranosema locustae were evaluated as control agents for the pest migratory grasshopper Melanoplus sanguinipes under laboratory and greenhouse conditions. Third-instar grasshoppers, reared in the laboratory, were exposed up to fourteen days to wheat bran treated with different concentrations of each of the fungi alone or the two pathogens combined. In the greenhouse, nymphs were placed individually in cages where they were able to increase their body temperatures by basking in the sun in an attempt to inhibit the fungal infection, and treated with each pathogen alone or in combination. Mortality was recorded daily and presence of fungal outgrowth in cadavers was confirmed by recording fungal mycosis for two weeks' post-treatment (PT). For combination treatment, the nature of the pathogen interaction (synergistic, additive, or antagonistic effects) was also determined. In laboratory conditions, all treatments except P. locustae alone resulted in grasshopper mortality. The application of the pathogen combinations caused 75% and 77%, mortality for lower and higher concentrations, respectively than each of the pathogens alone. We infer a synergistic effect occurred between the two agents. In greenhouse conditions, the highest mortalities were recorded in combination fungal treatments with a M. brunneum dose (60% mortality) and with a combination of the two pathogens in which M. brunneum was applied at high rate (50%) two weeks after application. This latter combination also exhibited a synergistic effect. Exposure to the P. locustae treatment did not lead to mortality until day 14 PT. We infer that these pathogens are promising for developing a biopesticide formulation for rangeland pest grasshopper management.

Laboratory bioassays of vegetable oils as kairomonal phagostimulants for grasshoppers (Orthoptera: Acrididae).

Vegetable oils have kairomonal attractant properties to grasshoppers primarily due to the presence of linoleic and linolenic fatty acids. These fatty acids are dietary essentials for grasshoppers and, once volatilized, can be detected by the insects' olfactory receptors. A laboratory bioassay method has been developed to identify vegetable oils that have fatty acid profiles similar to grasshoppers and that induce grasshopper attraction and feeding. Such oils could be useful kairomonal adjuvants and/or carriers for acridicide formulations. Three sets of laboratory bioassays demonstrated that the addition of a standard aliquot of different vegetable oils resulted in varying degrees of grasshopper feeding on otherwise neutral substrates. Addition of olive oil stimulated the greatest feeding in all three sets of assays, regardless of the age of the tested insects. Furthermore, addition of canola or flax oils markedly enhanced grasshopper feeding. These three oils--i.e., olive, canola, and flax oil--proved to be the best performing grasshopper stimulants. A second group of oils included rapeseed-flax mix and rapeseed oils; however, their performance was not as consistent as oils in the first group--especially with regard to nymphal feeding. A third group of oils consisted of soybean, corn, peanut, and sunflower oil. Theoretical expectations regarding these oils varied wildly, suggesting that the results of a single bioassay should be cautiously interpreted as being negative.

Mapping locust habitats in the Amudarya River Delta, Uzbekistan with multi-temporal MODIS imagery.

Reed beds of Phragmites australis in the River Amudarya delta near the Aral Sea constitute permanent breeding areas of the Asian Migratory locust, Locusta migratoria migratoria. Every year, thousands of hectares are treated with broad-spectrum insecticides to prevent locust swarms from damaging crops in adjacent areas. To devise efficient locust monitoring and management plans, accurate and updated information about the spatial distribution of reeds is necessary. Given the vast geographic extent of the delta, traditional, ground survey methods are inadequate. Remotely sensed data collected by the MODIS sensor aboard the TERRA satellite provide a useful tool to characterize the spatial distribution of reeds. Multi-temporal MODIS data, collected at different times of the growing season, were used to generate spectral-temporal signatures for reeds and other land cover classes. These spectral-temporal signatures were matched with reed phenology. MODIS information was digitally classified to generate a land cover map with an overall accuracy of 74%. MODIS data captured 87% of the ground-verified reed locations. Estimates derived from MODIS data indicate that 18% of the study area was covered by reeds. However, high commission error resulted from misclassification of reeds mixed with shrubs class and shrubs class as reeds. This could have resulted in overprediction of the area covered by reeds. Additional research is needed to minimize the overlap between reeds and other vegetation classes (shrubs, and reed and shrub mix). Nevertheless, despite its relatively low spatial resolution (250 m), multi-temporal MODIS data were able to adequately capture the distribution of reeds. Instead of blanketing the fragile wetland ecosystem of the Amudarya delta with chemical anti-locust treatments, plant protection specialists can use this information to devise ecologically sound pest management plans aimed at reducing the adverse environmental impact in the zone of the Aral Sea ecological catastrophe. MODIS methodology to identify reed stands can be applicable to the Migratory locust habitats in other geographic areas.