We contrasted body condition, and age-specific reproduction and mortality b
etween a growing population of sea otters (Enhydra lutris) at Kodiak Island
and a high-density near-equilibrium population at Amchitka Island, Alaska.
We obtained data from marked individuals, population surveys, and collecti
ons of beach-cast carcasses. Mass:length ratios indicated that females (but
not males) captured in 1992 at Amchitka were in poorer condition than thos
e captured at Kodiak in 1986-1987. In 1993, the condition of females at Amc
hitka improved in apparent response to two factors: (1) an episodic influx
of Pacific smooth lumpsuckers, Aptocyclus ventricocus, from the epi-pelagic
zone, which otters consumed; and (2) an increase in the otters' benthic in
vertebrate prey resulting from declining otter numbers. Reproductive rates
varied with age (0.37 [CI = 0.21 to 0.53] births female(-1) yr(-1) for 2-3-
yr-olds, and 0.83 [CI = 0.69 to 0.90] for females greater than or equal to
4 yr old), and were similar at both areas. Weaning success (pups surviving
to greater than or equal to 120 d), in contrast, was almost 50% lower at Am
chitka than at Kodiak and for females greater than or equal to 4 yr of age
was 0.52 (CI = 0.38 to 0.66) vs 0.94 (CI = 0.75 to 0.99), respectively. Six
ty-two percent of the preweaning pup losses at Amchitka occurred within a m
onth of parturition and 79% within two months. Postweaning survival was als
o low at Amchitka as only 18% of instrumented pups were known to be alive o
ne year after mother-pup separation. Adult survival rates appeared similar
at Amchitka and Kodiak. Factors affecting survival early in life thus are a
primary demographic mechanism of population regulation in sea otters. By m
aintaining uniformly high reproductive rates over lime and limiting investm
ent in any particular reproductive event, sea otters can take advantage of
unpredictable environmental changes favorable to pup survival. This strateg
y is consistent with predictions of "bet-hedging" life history models.