“…Such strong suppression of sexual morph production has also been shown in other aphids, e.g., A. forbesi in southern North America, Aphis chloris and M. viciae collected from England, and Myzus persicae in Greece (Lees, 1960;Marcovitch, 1924;Margaritopoulos et al, 2002;Wilson, 1938). Lees (1960) suggested that a seasonal timer for sexual morph production is adaptive to avoid producing sexual morphs under short days in early spring.…”
Section: Discussionmentioning
confidence: 99%
“…Similar phenomena have been reported in other aphid species. In many previous studies, however, it was unclear whether the number of days or the number of generations from hatching is important (Campbell and Tregidga, 2006;Dixon, 1972Dixon, , 1971Dixon and Glen, 1971;Lushai et al, 1996;Margaritopoulos et al, 2002;Wilson, 1938). Temperature affects the duration for which the seasonal timer can function in M. viciae, whereas photoperiod has no effect on the duration in Aphis rubicola (Brodel & Schaefers 1979;Lees 1960).…”
Many aphid species switch reproductive modes seasonally, with the sexual generations appearing in autumn. Sexual generations are induced by short days. It has been reported that the appearance of sexual morphs is suppressed by a transgenerational factor (a seasonal timer) over several generations after hatching from overwintered eggs. The present study examined whether the seasonal timer measures the number of days from hatching or the number of generations from hatching using the pea aphid, Acyrthosiphon pisum Harris (Homoptera: Aphididae). Effects of temperature and photoperiod on the seasonal timer were also examined by successive rearing. The ability to produce sexual morphs was strongly suppressed in stem mothers (the foundress generation), and gradually recovered over successive generations produced during a few months. The duration for which the seasonal timer could function depended on the number of days from hatching and temperature, but not on photoperiod or the number of generations from hatching. We thus showed in a single study that the seasonal timer of the pea aphid has all the physiological characteristics shown in separate studies in different aphid species.
“…Such strong suppression of sexual morph production has also been shown in other aphids, e.g., A. forbesi in southern North America, Aphis chloris and M. viciae collected from England, and Myzus persicae in Greece (Lees, 1960;Marcovitch, 1924;Margaritopoulos et al, 2002;Wilson, 1938). Lees (1960) suggested that a seasonal timer for sexual morph production is adaptive to avoid producing sexual morphs under short days in early spring.…”
Section: Discussionmentioning
confidence: 99%
“…Similar phenomena have been reported in other aphid species. In many previous studies, however, it was unclear whether the number of days or the number of generations from hatching is important (Campbell and Tregidga, 2006;Dixon, 1972Dixon, , 1971Dixon and Glen, 1971;Lushai et al, 1996;Margaritopoulos et al, 2002;Wilson, 1938). Temperature affects the duration for which the seasonal timer can function in M. viciae, whereas photoperiod has no effect on the duration in Aphis rubicola (Brodel & Schaefers 1979;Lees 1960).…”
Many aphid species switch reproductive modes seasonally, with the sexual generations appearing in autumn. Sexual generations are induced by short days. It has been reported that the appearance of sexual morphs is suppressed by a transgenerational factor (a seasonal timer) over several generations after hatching from overwintered eggs. The present study examined whether the seasonal timer measures the number of days from hatching or the number of generations from hatching using the pea aphid, Acyrthosiphon pisum Harris (Homoptera: Aphididae). Effects of temperature and photoperiod on the seasonal timer were also examined by successive rearing. The ability to produce sexual morphs was strongly suppressed in stem mothers (the foundress generation), and gradually recovered over successive generations produced during a few months. The duration for which the seasonal timer could function depended on the number of days from hatching and temperature, but not on photoperiod or the number of generations from hatching. We thus showed in a single study that the seasonal timer of the pea aphid has all the physiological characteristics shown in separate studies in different aphid species.
“…Values indicated by different letters are significantly different (P < 0.05 by the Tukey HSD test of arcsine-square root transformed data). Wilson, 1938). In Trichogramma species, at least under the circumstances of the present study, the diapause-averting maternal effect was also practically absolute.…”
Section: Discussionmentioning
confidence: 81%
“…The similar results were obtained in experiments with Aphis chloris Koch. Aphis rubicola Oestlund, Drepanosiphum platanoides (Schrank), Eucallipterus tiliae L., Myzus persicae (Sulzer), and Phorodon humuli (Schrank) although in these aphids, the ability to produce sexuales gradually increased over several generations (Brodel and Schaefers, 1979;Campbell and Tregidga, 2006;Dixon, 1971Dixon, , 1972Margaritopoulos et al, 2002;Wilson, 1938). It is interesting that we have found both gradual (in T. principium) and relatively rapid (in T. telengai) waning of the maternal restraining effect.…”
Section: Discussionmentioning
confidence: 84%
“…It is known that in several insect species the incidence of diapause among the progeny of females that had undergone diapause was relatively low or even zero despite the strong diapause-inducing conditions (Campbell and Tregidga, 2006;Dixon, 1971Dixon, , 1972Henrich and Denlinger, 1982;Jackson, 1963;Lees, 1960Lees, , 1966Lushai et al, 1996;Saunders et al, 2002;Saunders, 2010;Simmonds, 1947;Wilson, 1938). In some of the cited studies the stability of this effect was estimated.…”
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