Seasonal decline in mitochondrial plasticity in the three-spined stickleback

Mitochondrial plasticity enables ectothermic animals to maintain performance under changing thermal conditions, but whether this ability declines through adulthood is unknown. We explored changes in mitochondrial plasticity in the three-spined stickleback (Gasterosteus aculeatus), a temperate fish that in many populations has a single breeding season over which it produces multiple clutches and then dies. Wild-caught fish were exposed to one of three thermal regimes: remaining at 12°C, switching to constant warm (21°C) or diel cycling (12-21°C) for three weeks at either the beginning or end of the season. We quantified both phosphorylating and non-ATP-producing (OXPHOS and LEAK) respiration in isolated muscle mitochondria and oxidative control efficiency (OxCE). Early in the breeding season, young fish responded to elevated temperatures by adjusting both their capacity for ATP production and non-ATP-production respiration, but this mitochondrial plasticity declined over the season. OxCE was unaffected by time of season or temperature treatment. Changing body condition was unrelated to mitochondrial function. Our findings indicate that mitochondrial plasticity declines across adult life, potentially limiting thermal resilience in older individuals, the first time this has been reported in an ectotherm. This highlights the need to account for age-related physiological changes in capacity when predicting species' responses to environmental change.

Authors

Institutions

Publication Details

Journal
Biology Letters
Published
2026-01-21
DOI
https://doi.org/10.1098/rsbl.2025.0620
Primary Topic
Physiological and biochemical adaptations
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Seasonal decline in mitochondrial plasticity in the three-spined stickleback

Caroline Millet, P. Monaghan, Francisco Ruiz-Raya, Neil B. Metcalfe
Biology Letters
Physiological and biochemical adaptations
article

Seasonal decline in mitochondrial plasticity in the three-spined stickleback

Caroline Millet, P. Monaghan, Francisco Ruiz-Raya, Neil B. Metcalfe
article en

Abstract

Mitochondrial plasticity enables ectothermic animals to maintain performance under changing thermal conditions, but whether this ability declines through adulthood is unknown. We explored changes in mitochondrial plasticity in the three-spined stickleback (Gasterosteus aculeatus), a temperate fish that in many populations has a single breeding season over which it produces multiple clutches and then dies. Wild-caught fish were exposed to one of three thermal regimes: remaining at 12°C, switching to constant warm (21°C) or diel cycling (12-21°C) for three weeks at either the beginning or end of the season. We quantified both phosphorylating and non-ATP-producing (OXPHOS and LEAK) respiration in isolated muscle mitochondria and oxidative control efficiency (OxCE). Early in the breeding season, young fish responded to elevated temperatures by adjusting both their capacity for ATP production and non-ATP-production respiration, but this mitochondrial plasticity declined over the season. OxCE was unaffected by time of season or temperature treatment. Changing body condition was unrelated to mitochondrial function. Our findings indicate that mitochondrial plasticity declines across adult life, potentially limiting thermal resilience in older individuals, the first time this has been reported in an ectotherm. This highlights the need to account for age-related physiological changes in capacity when predicting species' responses to environmental change.

Biology LettersVol. 22(1)
University of Glasgow (GB)
University of Glasgow
Openalex Percentile: Top 85%
Physiological and biochemical adaptations
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.