“…However, mitochondria are also a major source of reactive oxygen species (ROS) that have the potential to cause oxidative damage (Brand, ). Temporary reductions in mitochondrial energy requirements, while providing short‐term energetic benefits, could potentially lead to associated increases in ROS levels, resulting in the long‐term costs of oxidative stress (Schull et al., ; Sorensen et al., ), potentially faster organismal senescence and hence constraints on future life history (Dowling & Simmons, ; Midwood, Larsen, Aarestrup, & Cooke, ; Monaghan, Metcalfe, & Torres, ; Selman, Blount, Nussey, & Speakman, ; Speakman et al., ). However, surprisingly little is known about these interactions as studies of mitochondrial energetics are generally conducted separately from those of ROS production (Sorensen et al., ; Zhang, Wu, & Klaassen, ; but see Brown & Staples, ; Chausse et al., ).…”