2013
DOI: 10.5253/078.101.0103
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Timing, Nest Site Selection and Multiple Breeding in House Martins: Age-Related Variation and the Preference for Self-Built Mud Nests

Abstract: Citation for published version (APA): Piersma, T. (2013). Timing, nest site selection and multiple breeding in House Martins: age-related variation and the preference for self-built mud nests. Ardea, 101(1), 23-32.

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Cited by 9 publications
(11 citation statements)
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“…Timing of breeding is one of the most important determinants of organismal fitness. Across a broad variety of taxa, the decision of when to breed determines what food resources will be abundant during each stage of reproduction (e.g., mink, Ben‐David 1997; sea ducks, Love et al 2010), the types and variety of nest sites available for breeding (e.g., house martins, Piersma 2013), the prevalence of parasites and predators that may harm the adult or its offspring (e.g., squirrels and hares, O’Donoghue and Boutin 1995; cliff swallows, Brown and Brown 1999), and the energy budget available for investment into other life history traits (e.g., wheatears, Low et al 2015). Previous researchers have documented the many costs associated with breeding at suboptimal times (blue tits, Nilsson 1994; sandpipers, McKinnon et al 2012; owls, Toyama et al 2015), and the importance of proper timing has become especially clear in circumstances in which environmental conditions have recently deviated from historical norms (e.g., flycatchers, Both and Visser 2001; swallows, Brown and Brown 2000; grouse, Ludwig et al 2006; deer, Plard et al 2014).…”
Section: Introductionmentioning
confidence: 99%
“…Timing of breeding is one of the most important determinants of organismal fitness. Across a broad variety of taxa, the decision of when to breed determines what food resources will be abundant during each stage of reproduction (e.g., mink, Ben‐David 1997; sea ducks, Love et al 2010), the types and variety of nest sites available for breeding (e.g., house martins, Piersma 2013), the prevalence of parasites and predators that may harm the adult or its offspring (e.g., squirrels and hares, O’Donoghue and Boutin 1995; cliff swallows, Brown and Brown 1999), and the energy budget available for investment into other life history traits (e.g., wheatears, Low et al 2015). Previous researchers have documented the many costs associated with breeding at suboptimal times (blue tits, Nilsson 1994; sandpipers, McKinnon et al 2012; owls, Toyama et al 2015), and the importance of proper timing has become especially clear in circumstances in which environmental conditions have recently deviated from historical norms (e.g., flycatchers, Both and Visser 2001; swallows, Brown and Brown 2000; grouse, Ludwig et al 2006; deer, Plard et al 2014).…”
Section: Introductionmentioning
confidence: 99%
“…2005, Imlay et al . 2018), although lower than the 91% nest success rate for House Martins observed by Piersma (2013). Our data suggest that the proportion of second broods may have declined.…”
Section: Discussionmentioning
confidence: 57%
“…Although triple‐brooding has been reported in studies elsewhere in Europe (Pajuelo et al . 1992, Piersma 2013), we believe this is the first study to provide evidence of triple brooding attempts for House Martins breeding in the UK. Using the probability of attempting two broods and the probability of nest success as measures of breeding performance, we show that the breeding performance of House Martins is driven by a combination of nest‐specific, landscape and weather variables.…”
Section: Discussionmentioning
confidence: 67%
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“…Why do House Martins Delichon urbicum prefer stinking old mud nests over clean strong artificial nests made of wood-concrete? Why do they choose the very nests that carry a load of louse fly Crataerina hirundinis pupae, parasites which as soon as they feel the warmth of returning martins will develop into serious bloodsucking monsters (Summers 1975, Piersma 2013?…”
mentioning
confidence: 99%