2017
DOI: 10.1111/1365-2435.12818
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Beyond thermal limits: comprehensive metrics of performance identify key axes of thermal adaptation in ants

Abstract: Summary How species respond to temperature change depends in large part on their physiology. Physiological traits, such as critical thermal limits (CTmax and CTmin), provide estimates of thermal performance but may not capture the full impacts of temperature on fitness. Rather, thermal performance likely depends on a combination of traits—including thermal limits—that vary among species. Here, we examine how thermal limits correlate with the main components that influence fitness in ants. First, we compare h… Show more

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Cited by 66 publications
(58 citation statements)
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“…On the one hand, thermal performance traits of workers shape ant ecology and distributions at local (Cerdá, Retana, & Cros, ; Kaspari et al, ; Talbot, ) and biogeographic scales (Arnan & Blüthgen, ; Arnan, Blüthgen, Molowny‐Horas, & Retana, ; Diamond et al, ). However, colony‐level performance is also governed by a capacity for thermoregulation (Baudier & O'Donnell, ) since colonies can use nest architecture to thermally manipulate larval development rates (Penick & Tschinkel, ) and shift colony growth rates (Penick, Diamond, Sanders, & Dunn, ). The buffering effects of colony‐level thermoregulation may be especially important to understanding our results, since high‐elevation habitats can have high diurnal variance in air temperatures that may select against high MR Q 10 values in ectotherms according to Jensen's inequality (Ruel & Ayres, ).…”
Section: Discussionmentioning
confidence: 99%
“…On the one hand, thermal performance traits of workers shape ant ecology and distributions at local (Cerdá, Retana, & Cros, ; Kaspari et al, ; Talbot, ) and biogeographic scales (Arnan & Blüthgen, ; Arnan, Blüthgen, Molowny‐Horas, & Retana, ; Diamond et al, ). However, colony‐level performance is also governed by a capacity for thermoregulation (Baudier & O'Donnell, ) since colonies can use nest architecture to thermally manipulate larval development rates (Penick & Tschinkel, ) and shift colony growth rates (Penick, Diamond, Sanders, & Dunn, ). The buffering effects of colony‐level thermoregulation may be especially important to understanding our results, since high‐elevation habitats can have high diurnal variance in air temperatures that may select against high MR Q 10 values in ectotherms according to Jensen's inequality (Ruel & Ayres, ).…”
Section: Discussionmentioning
confidence: 99%
“…a), perhaps explaining the increased activity of the ant Crematogaster lineolata —which made up >50% of pitfall captures and has a relatively high thermal tolerance (Penick et al. )—on plots with less plant biomass.…”
Section: Discussionmentioning
confidence: 99%
“…Surface temperature and solar radiation were reduced only on plots with increased plant biomass (Fig. 1a), perhaps explaining the increased activity of the ant Crematogaster lineolata-which made up >50% of pitfall captures and has a relatively high thermal tolerance (Penick et al 2017)-on plots with less plant biomass.…”
Section: Arthropod Abundance and Activitymentioning
confidence: 99%
“…Soil temperature also appeared to be the most important factor driving ant discovery of, and recruitment to, food (see also Dunn et al 2007). One confounding factor, however, that may shape the foraging behavior of ants is colony size as both the number of workers produced (Markin 1970, Tschinkel 1993 and the speed at which broods develop (Porter 1988, Penick et al 2017) changes with temperature throughout the year. In future studies, disentangling how colony size contributes to the nutritional demands of ant colonies across temporal changes in temperature will undoubtedly result in new and exciting insights.…”
Section: Performance Integrates Over Different Measures Of Environmenmentioning
confidence: 99%