Parental stress often has long-term consequences for offspring. However, the mechanisms underlying these effects and how they are shaped by conditions offspring subsequently experience are poorly understood. Telomeres, which often shorten in response to stress and predict longevity, may contribute to, and/or reflect these cross-generational effects. Traditionally, parental stress is expected to have negative effects on offspring telomeres, but experimental studies in captive animals suggest that these effects may depend on the subsequent conditions that offspring experience. Yet, the degree to which parental stress influences and interacts with stress experienced by offspring to affect offspring telomeres and survival in free-living organisms is unknown. To assess this, we experimentally manipulated the stress exposure of free-living parent and offspring house sparrows ( Passer domesticus ). We found a weak, initial, negative effect of parental stress on offspring telomeres, but this effect was no longer evident at the end of post-natal development. Instead, the effects of parental stress depended on the natural sources of stress that offspring experienced during post-natal development whereby some outcomes were improved under more stressful rearing conditions. Thus, the effects of parental stress on offspring telomeres and survival are context-dependent and may involve compensatory mechanisms of potential benefit under some circumstances.

Telomeres, protective caps at the end of chromosomes, are often positively related to lifespan and are thought to be an important mechanism of organismal aging. To better understand the casual relationships between telomere length and longevity, it is essential to be able to experimentally manipulate telomere dynamics (length and loss rate). Previous studies suggest that exposure to TA‐65, an extract from the Chinese root Astragalus membranaceus, activates telomerase, lengthens telomeres, increases the growth of keratin‐based structures, and boosts the immune system in adults. However, telomere loss is expected to be greatest during early life but whether TA‐65 has similar effects during this life stage is currently unknown. Here, we experimentally exposed free‐living house sparrow (Passer domesticus) chicks to TA‐65 during post‐natal development and examined the effects on telomere length and loss, growth of keratin‐based structures, and a measure of cellular immunity. Contrary to expectation, the growth of keratin‐based structures was reduced in TA‐65 chicks and in the second year of the study, chicks exposed to TA‐65 experienced more telomere loss than controls. Thus, the effects of TA‐65 on telomeres and keratin‐based structures differ across life stages and future research will be necessary to determine the mechanisms underlying these age‐specific effects.