2003
DOI: 10.1186/1475-2875-2-20
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Egg hatching, larval movement and larval survival of the malaria vector Anopheles gambiae in desiccating habitats

Abstract: Background: Although the effects of rainfall on the population dynamics of the malaria vector Anopheles gambiae have been studied in great detail, the effects of dry periods on its survival remain less clear.

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Cited by 59 publications
(24 citation statements)
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“…Until recently, aestivation in African anophelines has been discounted by most entomologists, although winter diapause in temperate malaria vectors has been well-documented (Jetten and Takken, 1994), and a few studies provided evidence consistent with it in Sudan (Omer and Cloudsley-Thompson, 1968, 1970). In part, this stemmed from studies conducted in areas that experience a “mild dry season,” during which some larval sites remain available within 5-10 km radius (Charlwood et al, 2000; Jawara et al, 2008; Koenraadt et al, 2003; Minakawa et al, 2001; Ramsdale and Fontaine, 1970a, b; Sogoba et al, 2007). Although less abundant, constantly available larval sites during the dry season probably act as a strong selection force against aestivation.…”
Section: Discussionmentioning
confidence: 99%
“…Until recently, aestivation in African anophelines has been discounted by most entomologists, although winter diapause in temperate malaria vectors has been well-documented (Jetten and Takken, 1994), and a few studies provided evidence consistent with it in Sudan (Omer and Cloudsley-Thompson, 1968, 1970). In part, this stemmed from studies conducted in areas that experience a “mild dry season,” during which some larval sites remain available within 5-10 km radius (Charlwood et al, 2000; Jawara et al, 2008; Koenraadt et al, 2003; Minakawa et al, 2001; Ramsdale and Fontaine, 1970a, b; Sogoba et al, 2007). Although less abundant, constantly available larval sites during the dry season probably act as a strong selection force against aestivation.…”
Section: Discussionmentioning
confidence: 99%
“…The daily mortality rate for eggs assumes that approximately half (~51%) of eggs hatch after 3 days, below the estimated hatch rate in controlled laboratory conditions [47] to account for predation. While the daily mortality rate for eggs is fixed (d e = 0.2) and age-dependent for adults (see below), we incorporate density dependence in larval mortality as a sigmoidal increase with the larval population size (S3D Fig): where d l min = 0.035 [57] is the baseline daily larval mortality rate, d l max = 0.4 is the maximum daily larval morality [57], n l is the total number of larvae, K = 10 4 is the equilibrium larval population size under no intervention, and the shape of the function is determined by the constants: c 1 = 0.05 to begin at the baseline daily mortality rate; c 2 = 3.4 to control steepness of the curve, and c 3 = 2 to control position of the curve, were chosen so the mortality rate at a population size of K results in exact replacement.…”
Section: Methodsmentioning
confidence: 99%
“…Meanwhile, investigations of population genetics ruled out severe demographic bottlenecks in areas with strong seasonal fluctuations on the abundance of these mosquitoes. These results suggest that a significant number of adult specimens survive locally during the dry season (Simard et al, 2000;Taylor et al, 1993), as the pre-imaginal stages (eggs, larvae and pupae) are not able to survive without water (Koenraadt et al, 2003;Minakawa et al, 2001). Hence, it was generally proposed that mosquito populations can be maintained in large numbers during the dry season via aestivating females that do not reproduce (Holstein, 1954;Lehmann et al, 2010;Omer and Cloudsley-Thompson, 1970), and thus survive the challenging desiccating environmental conditions.…”
Section: Introductionmentioning
confidence: 90%