Ageing is ubiquitous across living organisms, leading to behavioural changes throughout life [1][2][3][4] ("behavioural ageing"). Younger, sexually immature individuals tend to differ from older, mature individuals in a number of behavioural traits, including how they move (e.g., flight performance 5 ) and how they interact with conspecifics (e.g., strength of social interactions 6,7 ). Such behavioural changes may influence space use 3,8 , the spread of infectious diseases 1 , and even the lifespan of individuals 9 .Behavioural changes with age may also play an important role in how populations adjust to environmental change: young individuals may adopt novel behaviours and be the agents of change 10,11 , while old individuals, with their accumulated knowledge and experience, may adjust to the environment by shifting behavioural strategies over their lifetimes [12][13][14] . Despite the importance of understanding behavioural ageing in nature, most ecological studies focus on binary comparisons between young and old animals, failing to track individuals throughout their lives 15 . Specifically, longitudinal studies that follow long-lived animals throughout most of their lives are rare, mostly due to methodological contraints 15 . This gap hinders the identification of gradual and non-monotonic behavioural changes in the wild or the mechanisms that underlie population-level ageing patterns.Research on behavioural ageing reveals a spectrum of patterns at the population level (Figure 1): some behaviours remain fixed throughout life 16 , while others change, either gradually 2 , or drastically at specific ages (e.g., early 17,18 or late in life 19,20 ; the latter usually associated with senescence and loss of physiological or physical capacities 21,22,3 , Figure 1A). Population-level behavioural changes with age can arise from two, non-mutually exclusive mechanisms. First, individuals may change their behaviour throughout their lifetimes (behavioural plasticity 23,24,6 ).Second, natural selection may act against behaviours that can confer lower fitness, resulting in differential mortality (or selective disappearance) of particular phenotypes 25,26 . Such selection may result in changes to the behavioural composition of the population with increasing age, without within-individual behavioural plasticity 27,28 (Figure 1B). Ultimately, examining the patterns and