W. Jedrzejewski et al., WEASEL POPULATION RESPONSE, HOME-RANGE, AND PREDATION ON RODENTS IN ADECIDUOUS FOREST IN POLAND, Ecology, 76(1), 1995, pp. 179-195
Numerical responses of the weasel Mustela nivalis to the changes in po
pulation density of forest rodents (bank vole Clethrionomys glareolus
and yellow-necked mouse Apodemus flavicollis) and predation by weasels
were studied in the pristine deciduous forests of Bialowieza National
Park, eastern Poland, in 1985 through 1992. The rodents experienced 5
yr of noncyclic (seasonal) fluctuations (autumn density 23-74 rodents
/ha) and 2 yr of outbreak and crash (triggered by synchronous heavy cr
op of oak, hornbeam, and maple seeds). Autumn numbers of rodents excee
ded 300 individuals/ha during the outbreak and dropped to 8 individual
s/ha in the following autumn. Weasels were censused by livetrapping in
summer and by snowtracking on an 11.2 km(2) grid of transects in wint
er. Radiotracking of 12 weasels in 1990 and 1991 yielded estimates of
home ranges and daily movement distances, which were combined with sno
wtracking and livetrapping data to estimate densities during 7 yr. Est
imated winter density of weasels varied from 5.2 to 27.3 individuals/1
0 km(2) in December and declined to 0-19.1 individuals/10 km(2) by ear
ly spring (March). Midsummer (July/August) indices of weasel numbers w
ere extremely variable and corresponded to 41.9-47.6 individuals/10 km
(2) in years with moderate density of rodents, 101.7 individuals/10 km
(2) during the rodent outbreak and 19.1 individuals/10 km(2) during th
e crash. Increase of weasel numbers from spring to midsummer was posit
ively related to the spring numbers of rodents. Autumn and winter decl
ine of weasel numbers was not related to rodent density changes. Durin
g the outbreak and crash of the rodent population, the numbers of weas
els and rodents (both sampled at 2-3 mo intervals) were positively cor
related (P < 0.0005) with no time lag. Home ranges of male weasels rad
iotracked during the rodent outbreak were 11-37 ha (minimum convex pol
ygon), compared to 117-216 ha during the crash year. The predator/prey
ratio varied from 0 to 2.5 weasels/1000 rodents. The ratio was highes
t at low densities of rodents. With increasing numbers of rodents, the
ratio declined, since rodent population growth was overwhelmingly fas
ter than weasel population growth. In the 7 autumn-winter seasons (1 O
ctober-15 April), weasels removed, on average, 1.6 to 9.5 rodents from
each hectare, i.e., from 2 to 28% of autumn numbers of rodents. Winte
r predation by weasels was heaviest at rodent density of approximate t
o 20 individuals/ha. At lower densities of rodents, the number of weas
els was restricted by food shortage and the role of their predation ra
pidly declined. At high rodent densities, the rodent numbers by far ex
ceeded the predatory capacity of weasels and predation percentage decl
ined again. Weasel predation in relation to rodent density has the sam
e pattern in geographic zones ranging from Turkmen deserts to European
farmlands and forests.