1984
DOI: 10.1016/0022-1910(84)90114-8
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The effects of mating, exogenous juvenile hormone and a juvenile hormone analogue on pheromone titre, calling and oviposition in the omnivorous leafroller moth (Platynota stultana)

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Cited by 87 publications
(34 citation statements)
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“…If neighboring females interfere with a focal female's mating efforts, selection toward earlier calling can intensify in a manner analogous to earlier arrival of migratory organisms when the number of competitors increases (Kokko et al 2006). Although many empirical studies have measured the percentage of females calling (e.g., Webster and Cardé 1982;Babilis and Mazomenos 1992;Kamimura and Tatsuki 1993;Ming et al 2007), more information on their spatial arrangement could prove useful. Females can potentially use cues other than their own mating status to adjust signaling effort: if females can perceive the signals of competing females, there is potential for more complex signaling strategies than the ones modeled by us (Harari et al 2011).…”
Section: Discussionmentioning
confidence: 99%
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“…If neighboring females interfere with a focal female's mating efforts, selection toward earlier calling can intensify in a manner analogous to earlier arrival of migratory organisms when the number of competitors increases (Kokko et al 2006). Although many empirical studies have measured the percentage of females calling (e.g., Webster and Cardé 1982;Babilis and Mazomenos 1992;Kamimura and Tatsuki 1993;Ming et al 2007), more information on their spatial arrangement could prove useful. Females can potentially use cues other than their own mating status to adjust signaling effort: if females can perceive the signals of competing females, there is potential for more complex signaling strategies than the ones modeled by us (Harari et al 2011).…”
Section: Discussionmentioning
confidence: 99%
“…Further, obviously all of these factors can be strongly influenced by the weather and climate (McNeil 1991;Pellegrino et al 2013), and mate-searching males are known to navigate pheromone plumes of rather complex filamentous structure (e.g., Liu and Haynes 1992). Females can simply modify male arrival rates by choosing not to call (e.g., after mating; Webster and Cardé 1984). Here we do not focus on the postmating response, since it may be influenced by either male manipulation of female receptivity or the females' choices.…”
Section: A Theoretical Approach To Adaptive Variation In Female Pheromentioning
confidence: 99%
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“…If mating is delayed, the germ cells within the germarium disorganize and cell death occurs (Berger and Cruz-Landim 2012;. In several insects, mating is the primary factor that triggers oocyte ripening in the ovary, indicating the presence of factors in seminal fluid that trigger oogenesis (Ando et al 1996;Coffelt and Vick 1987;Fan et al 1999;Foster 1993;Giebultowicz et al 1991;Rafaeli and Gileadi 1995;Raina et al 1994;Shorey et al 1968;Webster and Carde 1984). Nonetheless, when analyzing mucus gland secretions, which are introduced with semen into the genital tract of honey bee queens, Colonello and Hartfelder (2003) did not find evidence that drone accessory gland proteins are necessary for ovarian development in A. mellifera .…”
Section: Discussionmentioning
confidence: 99%
“…Chemical substances which affect behavior of insects following mating have been found in a lepidopteran (Webster & Carde, 1984); an ichneumon wasp, Venturia (Nemeritis) canescens (Gravenhorst) (where heneicosane was involved) (Mudd et al, 1982) ; and the dipteran Drosophila, involving enzymes (Mane et al, 1983 ;Richmond & Senior, 1981). Prostaglandins, derivatives of certain polyunsaturated fatty acids, alter egg laying behavior in crickets (Stanley-Samuelson & Loher, 1986).…”
mentioning
confidence: 98%