Recreation negatively affects wildlife by influencing animal behavior vital to reproduction and survival. Such nonconsumptive effects of perceived predation risk are mainly studied in ground-breeding birds. However, if antipredator responses characterize bird species generally, so should nonconsumptive effects of perceived predation associated with human recreation. Moreover, as individuals consistently differ in behaviors linked to antipredator responses, they should also differ in responses to recreation, with bolder birds being less affected. To test this key prediction, we quantified effects of human recreation pressure on a cavity-breeding passerine. We uniquely quantified human recreation pressure over a substantial (8-year) period within 12 nest box populations of the great tit Parus major, assayed annually for reproductive parameters. We detected considerable spatial variation in recreation pressure. In plots with high recreation pressure, we found strong support for birds breeding further away from highly frequented paths and birds producing smaller clutches; we also found moderate support for birds producing fewer fledglings. These detrimental effects did not vary with behavioral proxies of an individual’s risk-taking phenotype (exploratory activity). This implies that effects of recreation pressure apply to the average bird, and extend to species (like forest birds) not previously considered.
Bird song transmits information required to defend territories and attract mates. These functions contribute to fitness by affecting survival and reproductive success. Singing is also costly due to physiological costs. We used observational data to evaluate support for the hypothesis that lower temperatures result in decreased singing behaviour in wild great tits due to increased energy consumption during cold conditions required for thermoregulation. More than 6,500 simulated territorial intrusions were performed over an 8‐year period in twelve nest box populations of great tits Parus major south of Munich, Germany. We measured song rate as well as the number of alarm calls and the aggressive response of territorial males to a simulated territorial intrusion. We found a decrease in song rate with decreasing current temperature, but also a concurrent increase in the number of alarm calls. Night temperature did not affect these acoustic traits. We conclude that warmer conditions allow birds to choose more energetically expensive (yet functionally superior) activities during territorial intrusions, thereby facilitating avoidance of physical aggressiveness during territorial intrusions.
Predictable behaviour (or ‘behavioural stability’) might be favoured in certain ecological contexts, for example when representing a quality signal. Costs associated with producing stable phenotypes imply selection should favour plasticity in stability when beneficial. Repeatable among‐individual differences in degree of stability are simultaneously expected if individuals differ in ability to pay these costs, or in how they resolve cost–benefit trade‐offs. Bird song represents a prime example, where stability may be costly yet beneficial when stable singing is a quality signal favoured by sexual selection. Assuming energetic costs, ecological variation (e.g. in food availability) should result in both within‐ and among‐individual variation in stability. If song stability represents a quality signal, we expect directional selection favouring stable singers. For a 3‐year period, we monitored 12 nest box plots of great tits Parus major during breeding. We recorded male songs during simulated territory intrusions, twice during their mate's laying stage and twice during incubation. Each preceding winter, we manipulated food availability. Assuming that stability is costly, we expected food‐supplemented males to sing more stable songs. We also expected males to sing more stable songs early in the breeding season (when paternity is not decided) and stable singers to have increased reproductive success. We found strong support for plasticity in stability for two key song characteristics: minimum frequency and phrase length. Males were plastic because they became more stable over the season, contrary to expectations. Food supplementation did not affect body condition but increased stability in minimum frequency. This treatment effect occurred only in 1 year, implying that food supplementation affected stability only in interaction with (unknown) year‐specific ecological factors. We found no support for directional, correlational or fluctuating selection on the stability in minimum frequency (i.e. the song trait whose stability exhibited cross‐year repeatability): stable singers did not have higher reproductive success. Our findings imply that stability in minimum frequency is not a fitness quality indicator unless males enjoy fitness benefits via pathways not studied here. Future studies should thus address the mechanisms shaping and maintaining individual repeatability of song stability in the wild.
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