1984
DOI: 10.2307/2408436
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Differences in Survivorship, Development Rate and Fertility Between the Longwinged and Wingless Morphs of the Waterstrider, Limnoporus canaliculatus

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Cited by 60 publications
(32 citation statements)
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“…The absence of a difference is caused by a "crossingover" of the m curves (i.e., the age schedules of reproduction) in the second week. Such an intersection was noted by Fairbairn (1988) for Gerris remigis, Limnoporus caniculatus, (data from Zera, 1984), and the cricket species, Gryllus firmus and Allonemobius fasciatus, (data from RoIl, 1984). It also occurs in Javesella pellucida (Mochida, 1973), Cavelerius saccharivorus (Fujisaki, 1986), and Horvathiolius gibbicollis (Soibreck, 1986), but not in the aphid species Setobion avenae, Metopolophium dirhodum (Wratten, 1977) and Aphisfabae (Dixon and Wratten, 1971).…”
Section: Discussionmentioning
confidence: 70%
“…The absence of a difference is caused by a "crossingover" of the m curves (i.e., the age schedules of reproduction) in the second week. Such an intersection was noted by Fairbairn (1988) for Gerris remigis, Limnoporus caniculatus, (data from Zera, 1984), and the cricket species, Gryllus firmus and Allonemobius fasciatus, (data from RoIl, 1984). It also occurs in Javesella pellucida (Mochida, 1973), Cavelerius saccharivorus (Fujisaki, 1986), and Horvathiolius gibbicollis (Soibreck, 1986), but not in the aphid species Setobion avenae, Metopolophium dirhodum (Wratten, 1977) and Aphisfabae (Dixon and Wratten, 1971).…”
Section: Discussionmentioning
confidence: 70%
“…Long-winged forms are significantly less fecund than flightless forms in grasshoppers (Ritchie et al, 1987), crickets (Mole & Zera, 1993;Tanaka & Suzuki, 1998), planthoppers (Denno et al, 1989, aphids (Dixon & Howard, 1986), seed bugs (Solbreck, 1986), water striders and veliids (Zera, 1984;Muraji & Nakasuji, 1988;Harada, 1992).…”
Section: Trade-off Between Reproduction and Dispersal Characteristicsmentioning
confidence: 99%
“…It is presumed to be a costly behavior, with adult reproduction suffering a trade-off in energy needed for adult flight apparatus construction and flight fuel versus ovarian development, or oogenesis (Rankin and Burchsted, 1992;Crowley and McLetchie, 2002;Ronce, 2007). The cost is usually manifested, especially in wing dimorphic species, as decreased reproductive output caused by a prolonged pre-oviposition period, decreased longevity, and decreased lifetime egg production (Dingle and Arora, 1973;Walters and Dixon, 1983;Roff, 1984;Zera, 1984;Zera and Mole, 1994). Physiological management of the migration-reproduction trade-off often includes a package of adaptations referred to as the oogenesis-flight syndrome, which was taken for many years as a fundamental trait of insect migrants (Johnson, 1969;Rankin et al, 1986Rankin et al, , 1994Colvin and Gatehouse, 1993;Keil et al, 2001;Gu et al, 2006;Lorenz, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…(ii) What is the effect of migration during the oviposition period on reproduction? Is there a reproductive cost to migration (Rankin and Burchsted, 1992;Dingle and Arora, 1973;Walters and Dixon, 1983;Roff, 1984;Zera, 1984;Zera and Mole, 1994)? (iii) Do adults have enough flight potential after mating and oviposition to support successful long-distance migration?…”
Section: Introductionmentioning
confidence: 99%