2004
DOI: 10.1139/z04-004
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Sex ratio estimation and survival analysis for Orthetrum coerulescens (Odonata, Libellulidae)

Abstract: There is controversy over whether uneven sex ratios observed in mature dragonfly populations are a mere artifact resulting from the higher observability of males. Previous studies have at best made indirect inference about sex ratios by analysis of survival or recapture rates. Here, we obtain direct estimates of sex ratio from capture–recapture data based on the Cormack–Jolly–Seber model. We studied Orthetrum coerulescens (Fabricius, 1798) at three sites in the Swiss Jura Mountains over an entire activity peri… Show more

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Cited by 16 publications
(9 citation statements)
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“…Similar results were observed in Coenagrion puella and Orthetrum coerulescens where males outnumbered females 3.5 and 1.6 times, respectively, and also were almost four times more likely to be recaptured than females (Anholt et al 2001;Kéry and Juillerat 2004). Differential habitat use by the different sexes could explain the recapture rates estimated for H. trinitatis, since males spend more time in visible places than females.…”
Section: Discussionsupporting
confidence: 75%
See 1 more Smart Citation
“…Similar results were observed in Coenagrion puella and Orthetrum coerulescens where males outnumbered females 3.5 and 1.6 times, respectively, and also were almost four times more likely to be recaptured than females (Anholt et al 2001;Kéry and Juillerat 2004). Differential habitat use by the different sexes could explain the recapture rates estimated for H. trinitatis, since males spend more time in visible places than females.…”
Section: Discussionsupporting
confidence: 75%
“…Modern Cormack-Jolly-Seber mark-recapture methods (CJS) allow for the independent assessment of recapture and survival rates (Lebreton et al 1992). The application of these methods has led to the general conclusion that, at least in some species, males have higher recapture rates than females, while survival rates are similar for both sexes (Kéry and Juillerat 2004). However, this argument cannot be used as a general explanation, since a lower survival rate of females during the pre-reproductive period seems to be the cause of the male-biased sex ratio in some populations, where survival and recapture rates are similar in both sexes at the reproductive period (Anholt 1997;Stoks 2001b).…”
Section: Introductionmentioning
confidence: 99%
“…Mortality rates of adults are quite high for most species, with most individuals living on average only a few days or weeks after they metamorphose into adults (Fincke 1982(Fincke , 1986(Fincke , 1994Anholt 1991Anholt , 1997Córdoba-Aguilar 1994;Bennett and Mill 1995b;Cordero 1995;Marden and Rowan 2000;Beukema 2002;Thompson and Fincke 2002). Also, because of the differences in breeding tactics of males and females, females sometimes have higher mortality rates than males (Bennett and Mill 1995b;Anholt 1997;Marden and Rowan 2000;Beukema 2002;Kery and Juillerat 2004;Córdoba-Aguilar et al 2006). Females of most species spend considerable time away from water bodies to forage and presumably to reduce harassment by males, but at the expense of greater mortality (Anholt 1997;Marden and Rowan 2000;Anholt et al 2001).…”
Section: Adultsmentioning
confidence: 99%
“…The resighting rate at the watercourse was very small (8.13%) with respect to other dragonflies like Somatochlora alpestris Selys (10.2%), Leucorrhinia hudsonica Selys (31%), and Orthetrum coerulescens Selys (40–55%) ( Knaus and Wildermuth 2002 , Kéry and Juillerat 2004 , Chin and Taylor 2009 ). Moreover, less than 1% of G. lucasii Selys tenerals (only males) were resighted as mature at the water and an even smaller proportion was recorded at their emergence site (philopatry).…”
Section: Discussionmentioning
confidence: 90%