A positive genetic correlation between basal metabolic rate (BMR) and maxim
al ((V) over dotO(2)max) rate of oxygen consumption is a key assumption of
the aerobic capacity model for the evolution of endothermy. We estimated th
e genetic (V-A, additive, and V-D, dominance), prenatal (V-N), and postnata
l common environmental (V-E) contributions to individual differences in met
abolic rates and body mass for a genetically heterogeneous laboratory strai
n of house mice (Mus domesticus). Our breeding design did not allow the sim
ultaneous estimation of V-D and V-N. Regardless of whether V-D or V-N was a
ssumed, estimates of V-A were negative under the full models. Hence, we fit
ted reduced models (e.g., V-A + V-N + V-E or V-A + V-E) and obtained new va
riance estimates. For reduced models, narrow-sense heritability (h(N)(2)) f
or BMR was <0.1, but estimates of h(2)(N) for (V) over dotO(2)max were high
er. When estimated with the V-A + V-E model, the additive genetic covarianc
e between (V) over dotO(2)max and BMR was positive and statistically differ
ent from zero. This result offers tentative support for the aerobic capacit
y model for the evolution of vertebrate energetics. However, constraints im
posed on the genetic model may cause our estimates of additive variance and
covariance to be biased, so our results should be interpreted with caution
and tested via selection experiments.