Dw. Thomas et al., METABOLIC RATES AND BODY-MASS CHANGES IN COMMON POORWILLS (PHALAENOPTILUS-NUTTALLII, CAPRIMULGIDAE), Ecoscience, 3(1), 1996, pp. 70-74
We studied field metabolic rate (FMR) and mass changes in nesting comm
on poorwills (Phalaenoptilus nuttallii; Caprimulgidae) using the doubl
y labelled water method. In June when poorwills were incubating a firs
t clutch, FMR for females was significantly lower than for males (fema
les: 28.3+/-3.0 kJ . d-1; males 85.0+/-12.7 kJ . d(-1)), but FMR did n
ot differ between the sexes in August (59.6+/-8.7 kJ . d(-1)) when bir
ds were incubating a second clutch. Mass change (MC) was significantly
correlated with FMR (MC = 1.548 - 0.031 . FMR) and birds achieved mas
s stability at FMR of 49.9 kJ . d(-1). The mass stable FMR of 49.9 kJ
. d(-1) is 3.0 x BMR (basal metabolic rare) and is only 54% of Nagy's
(1987; Ecological Monographs, 57: 111-128) allometric equation predict
ing FMR for non-passerines. These data support the idea that low BMR,
characteristic of poowills, results in low FMR. An analysis of mass ch
ange as a function of foraging and FMR suggests that poorwills forage
at a maximum rate of 200-300 sallies . night(-1) and that mass change
results from fat deposition or mobilization. When vigorously calling t
o defend territories in June, male poorwills have FMR of 5.1 X BMR, wh
ich ranks in the top 5% of FMR recorded for birds. We suggest that mal
es invest heavily in territorial displays and run a negative energy ba
lance through June, leading to observed mass loss.