2014
DOI: 10.1111/jeb.12342
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Size differentiation in Finnish house sparrows follows Bergmann's rule with evidence of local adaptation

Abstract: Bergmann's rule predicts that individuals are larger in more poleward populations and that this size gradient has an adaptive basis. Hence, phenotypic divergence in size traits between populations (P ST ) is expected to exceed the level of divergence by drift alone (F ST ). We measured 16 skeletal traits, body mass and wing length in 409 male and 296 female house sparrows Passer domesticus sampled in 12 populations throughout Finland, where the species has its northernmost European distributional margin. Morph… Show more

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Cited by 22 publications
(29 citation statements)
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“…Thus, with the exception of Robin, the results are broadly in agreement with Bergmann's rule. For female House Sparrow this result is consistent with published trends for the USA and Finland but unfortunately body mass was not used in these studies to enable a specific comparison of variation with latitude to be made (Johnston & Selander 1971, Brommer et al 2014.…”
Section: Discussionsupporting
confidence: 90%
See 1 more Smart Citation
“…Thus, with the exception of Robin, the results are broadly in agreement with Bergmann's rule. For female House Sparrow this result is consistent with published trends for the USA and Finland but unfortunately body mass was not used in these studies to enable a specific comparison of variation with latitude to be made (Johnston & Selander 1971, Brommer et al 2014.…”
Section: Discussionsupporting
confidence: 90%
“…For example, the House Sparrow Passer domesticus is a species that fits Bergmann's rule in the USA (Johnston & Selander 1971) and Finland (Brommer et al 2014). The Robin Erithacus rubecula is a sedentary native species and in contrast to House Sparrow, is commonly considered to exhibit only limited sexual dimorphism (Jovani et al 2012).…”
Section: Body Size Variables and Species Selectionmentioning
confidence: 99%
“…Under controlled conditions, phenotypic differences should be entirely due to additive genetic effects, so c/h 2 = 1 and P ST is equivalent to Q ST , and analogous to Q ST for a given quantitative trait (Wright, 1950). In wild populations, h 2 and c are usually difficult to estimate (Brommer, 2011) and nonadditive genetic effects such as selection can strongly influence the estimation of P ST (Brommer, 2011;Brommer, Hanski, Kekkonen, & Väisänen, 2014;Leinonen, Cano, Mäkinen, & Merilä, 2006;Pujol, Wilson, Ross, & Pannell, 2008). Consequently, we used a sequence of 100 values of c/h 2 between zero and two (Brommer, 2011).…”
Section: Phenotypic Variability and Traits Under Selectionmentioning
confidence: 99%
“…This was done separately in the seeder and resprouter groups of populations to detect differences in the P ST ÀF ST contrasts between regeneration forms. (1) that the proportion of total variance due to additive genetic effects across populations (c. scalar) equals the heritability of the trait (h 2 ) (Brommer, 2011;Brommer et al, 2014). Saether et al, 2007;Wojcieszek & Simmons, 2012), we used the 99% level to be more conservative, as P ST tends to overestimate Q ST (Brommer, 2011;Young, Evans & Simmons, 2011).…”
Section: P St àF St Analysismentioning
confidence: 99%
“…Although P ST ÀF ST comparisons are normally carried out using 95% confidence intervals (e.g. To do so, we used the approach of Brommer et al (2014) of calculating, for each trait from eqn. Confidence intervals were calculated by the BCa method and 5000 bootstrap iterations using the 'boot' package in R (Canty & Ripley, 2008).…”
Section: P St àF St Analysismentioning
confidence: 99%