Identification of the female sex pheromones of the moth, Chilo suppressalis
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Cited by (75)
Functional disparity of four pheromone-binding proteins from the plum fruit moth Grapholita funebrana Treitscheke in detection of sex pheromone components
2023, International Journal of Biological MacromoleculesCitation Excerpt :The sex pheromone components of Crambidae species are complex. The primary sex pheromone components of C. suppressalis consist of (Z)-11-hexadecenal, (E)-11-hexadecenal, and (Z)-13-octadecenal, and the secondary components consist of tetradecyl acetate and hexadecyl acetate [59]. In C. punctiferalis, another Crambidae species, the primary sex pheromone components contain (E)-8–10-hexadecenal and (Z)-10-hexadecenal [60], and the secondary components contain (E)-8–10-hexadecenol and hexadecanal [61].
Eleocharis dulcis (Burm.f) as a promising trap plant for the biocontrol of rice white stem borer, Scirpophaga innotata (Walker)
2021, Biological ControlCitation Excerpt :Around the world, the stem borers have been controlled by integrated pest management practices suitable for each species, but including the following basic outlay: 1) selection of an appropriate crop planting technique or scheme; 2) using insect pest resistant plants (Baloch and Abdullah, 2011); and 3) using natural enemies. Insecticides have less efficacy for controlling the notorious stem borers, including the white-stem borer of rice because chemicals are effective only during the very short period between egg-hatch and plant penetration (Nesbitt et al., 1975; Beevor et al., 1990; Howse et al., 1998). Van der Goot (1948) recorded three hymenopteran parasitoids, viz. Telenomus rowani (Gahan) (Scelionidae), Tetrasticus schoenobii Ferriere (Eulophidae), and Trichogramma japonicum Ashmead (Trichogrammatidae) as egg parasitoids of S. innotata.
Two general odorant binding proteins display high bindings to both host plant volatiles and sex pheromones in a pyralid moth Chilo suppressalis (Lepidoptera: Pyralidae)
2017, Journal of Asia-Pacific EntomologyCitation Excerpt :To determine the binding specificities of the two CsupGOBPs, 38 volatiles were selected as the ligands in the binding assays. These volatiles included rice plant volatiles reported in literatures (Du et al., 2005; Feng et al., 2010; Fujii et al., 2010; Lou et al., 2005; Obata et al., 1983; Widjaja et al., 1996; Zhang et al., 2014b), three female sex pheromones of C. suppressalis (Nesbitt et al., 1975), and some general plant volatiles (Bengtsson et al., 2001; Dudareva et al., 2004; Mei et al., 2007). Consistent with the male biased expression pattern, CsupGOBP2 showed strong binding affinities to all three sex pheromones (Ki = 0.36–0.64 μM), again suggesting the role in the perception of female sex pheromones.
Mating disruption to control the striped rice stem borer: Pheromone blend, dispensing technology and number of releasing points
2016, Journal of Asia-Pacific EntomologyCitation Excerpt :Currently in Spain, C. suppressalis is being controlled by using insect growth regulators and mating disruption or mass trapping methods, especially in environmentally protected areas. C. suppressalis pheromone was first identified as the aldehyde blend containing (Z)-11-hexadecenal (Z11-16:Ald) and (Z)-13-octadecenal (Z13-18:Ald) (Nesbitt et al., 1975; Ohta et al., 1976). It was later demonstrated that the attractant power of this blend was less efficient than that of virgin females.
Optimization of pheromone dispenser density for managing the rice striped stem borer, Chilo suppressalis (Walker), by mating disruption
2009, Crop ProtectionCitation Excerpt :The sex pheromone of female C. suppressalis was initially identified in 1975 as a binary mixture of (Z)-11-hexadecenal (Z11–16:Ald) and (Z)-13 octadecenal (Z13–18:Ald). The pheromone was present in female ovipositor extract (Nesbitt et al., 1975; Ohta et al., 1975, 1976). In 1983, another active compound of the sex pheromone from C. suppressalis, (Z)-9-hexadecenal (Z9–16:Ald), was discovered (Tatsuki et al., 1983).