A fast pace-of-life is traded off against a high thermal performance
The integration of life-history, behavioural and physiological traits into a 'pace-of-life syndrome' is a powerful concept in understanding trait variation in nature. Yet, mechanisms maintaining variation in 'pace-of-life' are not well understood. We tested whether decreased ther...
Main Authors: | , |
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Format: | Article |
Language: | English |
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NLM (Medline)
2022
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Online Access: | View Fulltext in Publisher |
LEADER | 02524nam a2200373Ia 4500 | ||
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001 | 10-1098-rspb-2021-2414 | ||
008 | 220425s2022 CNT 000 0 und d | ||
020 | |a 14712954 (ISSN) | ||
245 | 1 | 0 | |a A fast pace-of-life is traded off against a high thermal performance |
260 | 0 | |b NLM (Medline) |c 2022 | |
856 | |z View Fulltext in Publisher |u https://doi.org/10.1098/rspb.2021.2414 | ||
520 | 3 | |a The integration of life-history, behavioural and physiological traits into a 'pace-of-life syndrome' is a powerful concept in understanding trait variation in nature. Yet, mechanisms maintaining variation in 'pace-of-life' are not well understood. We tested whether decreased thermal performance is an energetic cost of a faster pace-of-life. We characterized the pace-of-life of larvae of the damselfly Ischnura elegans from high-latitude and low-latitude regions when reared at 20°C or 24°C in a common-garden experiment, and estimated thermal performance curves for a set of behavioural, physiological and performance traits. Our results confirm a faster pace-of-life (i.e. faster growth and metabolic rate, more active and bold behaviour) in the low-latitude and in warm-reared larvae, and reveal increased maximum performance, Rmax, but not thermal optimum Topt, in low-latitude larvae. Besides a clear pace-of-life syndrome integration at the individual level, larvae also aligned along a 'cold-hot' axis. Importantly, a faster pace-of-life correlated negatively with a high thermal performance (i.e. higher Topt for swimming speed, metabolic rate, activity and boldness), which was consistent across latitudes and rearing temperatures. This trade-off, potentially driven by the energetically costly maintenance of a fast pace-of-life, may be an alternative mechanism contributing to the maintenance of variation in pace-of-life within populations. | |
650 | 0 | 4 | |a article |
650 | 0 | 4 | |a cold stress |
650 | 0 | 4 | |a controlled study |
650 | 0 | 4 | |a damselfly |
650 | 0 | 4 | |a growth rate |
650 | 0 | 4 | |a larva |
650 | 0 | 4 | |a latitude |
650 | 0 | 4 | |a life history |
650 | 0 | 4 | |a life-history |
650 | 0 | 4 | |a metabolic rate |
650 | 0 | 4 | |a nonhuman |
650 | 0 | 4 | |a Odonata |
650 | 0 | 4 | |a rearing |
650 | 0 | 4 | |a structural equation modeling |
650 | 0 | 4 | |a structural equation modelling |
650 | 0 | 4 | |a swimming speed |
650 | 0 | 4 | |a syndromes |
650 | 0 | 4 | |a thermal physiology |
650 | 0 | 4 | |a trade-off |
700 | 1 | |a Stoks, R. |e author | |
700 | 1 | |a Tüzün, N. |e author | |
773 | |t Proceedings of the Royal Society B: Biological Sciences |