2010
DOI: 10.1111/j.1420-9101.2010.01994.x
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The diapause decision as a cascade switch for adaptive developmental plasticity in body mass in a butterfly

Abstract: Switch‐induced developmental plasticity, such as the diapause decision in insects, is a major form of adaptation to variable environments. As individuals that follow alternative developmental pathways will experience different selective environments the diapause decision may evolve to a cascade switch that induces additional adaptive developmental differences downstream of the diapause decision. Here, we show that individuals following alternative developmental pathways in a Swedish population of the butterfly… Show more

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Cited by 43 publications
(44 citation statements)
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“…Apart from their striking differences in colouration, the two generations also differ in body design, wing loading, dispersal propensity and resource allocation pattern (Fric and Konvicka 2002; Friberg and Karlsson 2010). The spring and summer generations of P. napi differ in dispersal ability and fecundity (Karlsson and Johansson 2008), as well as in mating propensity and sexual maturity at eclosion (Larsdotter Mellström et al 2010), whereas the different developmental pathways of P. aegeria differ in the number of eyespots present on the dorsal side of the hind wing (Shreeve 1987), as well as in body size and fecundity (Van Dyck and Wiklund 2002; Gotthard and Berger 2010). All these adaptive or nonadaptive, season-specific traits must be developed downstream of the decision whether to enter diapause or direct development, which may further explain why there is a point of no return after which the larvae cannot switch pathways after a certain size or age.…”
Section: Discussionmentioning
confidence: 99%
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“…Apart from their striking differences in colouration, the two generations also differ in body design, wing loading, dispersal propensity and resource allocation pattern (Fric and Konvicka 2002; Friberg and Karlsson 2010). The spring and summer generations of P. napi differ in dispersal ability and fecundity (Karlsson and Johansson 2008), as well as in mating propensity and sexual maturity at eclosion (Larsdotter Mellström et al 2010), whereas the different developmental pathways of P. aegeria differ in the number of eyespots present on the dorsal side of the hind wing (Shreeve 1987), as well as in body size and fecundity (Van Dyck and Wiklund 2002; Gotthard and Berger 2010). All these adaptive or nonadaptive, season-specific traits must be developed downstream of the decision whether to enter diapause or direct development, which may further explain why there is a point of no return after which the larvae cannot switch pathways after a certain size or age.…”
Section: Discussionmentioning
confidence: 99%
“…The offspring of two spring cohorts develop directly (without diapause) into two separated summer cohorts (Van Dyck and Wiklund 2002). In central Sweden this species is an obligatory pupal diapauser (Gotthard and Berger 2010), and typically appears in a single large generation per year, but occasionally flies in a partial, small, directly developing summer generation (Eliasson et al 2005). …”
Section: Methodsmentioning
confidence: 99%
“…However, it remains to be tested whether size polyphenism may be adaptive per se (i.e. if the relationship between size and fitness differs seasonally), something which has been suggested for some other 405 butterflies Karlsson 2010, Gotthard andBerger 2010). Nevertheless, the most likely ultimate reason for the between-generation differences in larval growth trajectories of I. podalirius appears to be related to the presence or absence of the 408 overwintering stage in the future development of the insect.…”
Section: Discussion 345mentioning
confidence: 99%
“…Individual insects that follow the two alternative pathways of direct and diapause development often display substantial phenotypic differences (Shapiro and references therein, Beldade & Brakefield ). Seasonal polyphenisms in morphology of insects with more than one generation per year are well known (Shapiro ) but until recently there have been few studies of how the expression of life‐history traits may differ among pathways (Van Dyck & Wiklund ; Musolin ; Gotthard & Berger ; Teder et al . ; Aalberg Haugen, Berger & Gotthard ).…”
Section: Introductionmentioning
confidence: 99%
“…; Aalberg Haugen, Berger & Gotthard ). It has been suggested that, depending on the degree of developmental independence among pathways, we might expect differential optimization of life‐history traits in response to the predictable difference in environment that the two classes of individuals will be subjected to (Gotthard & Berger ; Kivelä, Välimäki & Gotthard ). In fact, the developmental decision of pathway contains information about the expected future selective environment that can be used for alternative developmental regulation.…”
Section: Introductionmentioning
confidence: 99%