Search Results (3)

In this study, the effects of paraffin oil, copper hydroxide, copper oxychloride, wettable sulfur, Beauveria bassiana and deltamethrin, as a toxic reference treatment, on the survival and predation rate of M. pygmaeus were investigated. In each treatment, the prey were classified as slightly, partially or fully consumed. The mortality rate after contact exposure was high (66.6%) when nymphs were treated with copper hydroxide but much lower after residual exposure (6.6%). B. bassiana caused 53.3% and 46.6% mortality via contact and residual exposure, respectively. The total prey consumption was significantly lower in the pyrethroid reference treatment control and B. bassiana treatments. The highest percentage of slightly consumed prey was recorded in the toxic reference and B. bassiana treatments, that of partially consumed prey in the copper hydroxide treatment and, finally, that of fully consumed prey in the paraffin oil treatment. Therefore, assessing the sub-lethal effects by separating the prey killed into slightly, partially and fully consumed is a sensitive approach to detect impacts which otherwise may remain unnoticed. The results provide information for the most appropriate use of M. pygmaeus in IPM programs and introduce more sensitive approaches in the detection of side-effects of pesticides on M. pygmaeus and other hemipteran predators. Full article

Many predatory mites use insects for dispersal; however, their possible negative effects on insect hosts during transportation and on insect offspring while preying in the hosts’ habitats are still poorly understood. A recent study has revealed that the predatory mite Blattisocius mali can not only spread by means of drosophilid fruit flies but also feed on their bodies during dispersal. The aim of this study was to examine the capability of B. mali to prey upon the eggs of their fruit fly hosts and determine the effect of the egg’s age on the voracity of this predator. Drosophila melanogaster oviposited on agar media for 1 h and D. hydei for 8 or 16 h. During 10-h experiments with fifteen fly eggs per cage, a single female predator totally consumed on average 3.62 ± 0.673 “1-h” D. melanogaster eggs and 3.00 ± 0.612 “8-h” eggs of D. hydei, while it partially consumed 2.75 ± 0.586 and 3.00 ± 0.612 eggs of each fly species. In the experiments involving D. hydei, the predator totally destroyed a similar number of “8-h” and “16-h” eggs, but it partially consumed significantly more younger eggs than older eggs. Ethological observations showed that mites returned to some partially fed eggs, usually from the side where the first puncture was made, and only then did they consume them whole. Full article

Many organisms possess “secondary” compounds to avoid consumption or to immobilize prey. While the most abundant or active compounds are initially investigated, more extensive analyses reveal other “minor” compounds with distinctive properties that may also be of biomedical and pharmaceutical significance. Here, we present an initial in vitro investigation of the actions of two isomeric tetrahydropyridyl ring-containing anabasine analogs: isoanatabine, an alkaloid isolated from a marine worm, and anatabine, a relatively abundant minor alkaloid in commercial tobacco plants. Both compounds have a double bond that is distal to the piperidine ring nitrogen of anabasine. Racemic isoanatabine and anatabine were synthesized and their S- and R-enantiomers were isolated by chiral high pressure liquid chromatography (HPLC). Both isoanatabines displayed higher efficacies at α4β2 nicotinic acetylcholine receptors (nAChRs) relative to the anatabines; R-isoanatabine was most potent. Radioligand binding experiments revealed similar α4β2 nAChR binding affinities for the isoanatabines, but R-anatabine affinity was twice that of S-anatabine. While the two anatabines and S-isoanatabine were highly efficacious agonists at α7 nAChRs, R-isoanatabine was only a weak partial agonist. The four compounds share an ability to stimulate both α4β2 and α7 nAChRs, a property that may be useful in developing more efficacious drugs to treat neurodegenerative and other medical disorders. Full article