We estimated reproductive effort (energy expenditures for reproduction
, as opposed to maintenance) in Adelie penguins breeding at Palmer Sta
tion, Antarctica. Data on body composition changes and metabolic rate
were obtained using isotopic methods. Adelie breeding behavior consist
s of an initial courtship stage (during which both sexes fast), incuba
tion, the 'guard' stage (when chicks are 1 to 18-28 days old), and the
'creche' stage (from the end of guarding until chicks are 38-45 days
old). Both males and females lost considerable mass during the initial
stages of the reproductive season, but males fasted longer and lost m
ore mass. Mass losses of both sexes consisted of 66% depot fat and 34%
lean tissue. Mass and body composition remained constant once birds r
esumed feeding. The metabolic expenditure for the foraging necessary t
o accumulate the mass lost while fasting - one component of reproducti
ve effort - was about 63 MJ in males and 39 MJ in females. Field metab
olic rates (FMR) were low during courtship and while incubating, incre
asing more than 2-fold when birds resumed foraging. Although mean FMR
increased between incubation and the creche stage, differences between
stages were small and not significant. We used FMR data and an energy
balance model to estimate the cost of feeding chicks. Results suggest
a maintenance FMR of about 2.7 x basal metabolism (BMR), increasing t
o 3.4-3.6 x BMR during the creche stage. The reproductive effort (as m
etabolic expenditures) associated with feeding chicks is 31 MJ (males)
to 36 MJ (females). Cumulative reproductive effort is 94 MJ in males
and 75 MJ in females, or 5.3-6.2% of the annual energy budget. The rep
roductive effort devoted to chick care does not appear to be constrain
ed by physiological or time limitations. Instead, selection to reduce
the risk of predation may prevent the evolution of increased parental
care.