MANEN W VAN (2006) Use of winter-roosts, breeding numbers and reproduction. LIMOSA 79 (2): 53-62.
Long-eared Owls Asio otus were studied in the
northern Netherlands in 1986-2001, to evaluate
how diet composition affects the use of winter
roosts, numbers of breeding pairs, and reproduction.
The study area (2500 ha) is dominated
by farmland (both arable and grassland), complemented
with dry heathland, mixed woodlots,
some small villages and the edge of a town.
The area offers almost unlimited roosting and
nesting possibilities and foraging habitat is diverse.
Diet composition was studied by collecting
pellets at winter roosts or in breeding territories.
Owls were counted on winter-roosts every ten
days. From 1986-1996 presumably all roosts
were known. Territories were mapped by visiting
potential breeding sites in the early
evening, six times in January-April to detect
displaying birds, and three times in May-July
for begging young. Nests were searched for in
suitable breeding habitat.
Throughout the study period Short-tailed
Voles Microtus arvalis were the most important
prey species (69%; Fig. 1). Other prey included
Wood Mouse Apodemus sylvaticus (14%),
Common Vole Microtus agrestis (5.5%), Bank
Vole Clethrionomys glareolus (3.5%), birds
(3.0%) and Harvest Mouse Micromys minutus
(2.8%). Other species were represented in the
diet by less than 1%. The proportion of voles in
the diet was highest in late summer, declined in
autumn and winter, and was lowest in spring
(Fig. 2).
The number of winter roosts was nearly constant,
but the number of owls per roost varied
between years. The number of wintering owls
depended on the proportion of Short-tailed
Voles in their winter diet (October-December;
Fig. 3). The use of winter-roosts was described
by the period during which more than 50% of
the maximum number of owls was present at
the roost. There was a tendency that roosts
were established later and deserted earlier in
years with higher proportions of Short-tailed
Voles in their winter diet. When the owls spent
fewer days at the communal roosts, and left
roosts earlier, more breeding territories were
occupied (Fig. 4) and more young produced in
the following breeding season.
The number of breeding territories was related
to the percentage of Short-tailed Voles in the
diet in January-March (Fig. 5). There was also a
correlation between the average number of
young fledged per pair in the preceding breeding
season and the number of breeding pairs in
the subsequent spring, indicating that local offspring
tend to remain in the study area. No correlations
were found between breeding parameters
and the proportion of voles in the
summer diet. Percentage of successful pairs
and number of fledglings per brood were positively
correlated with the sum of the proportion
of voles and Wood Mice in the summer diet
(Fig. 6). Nevertheless, the exact role of prey
species other than Short-tailed Vole during the
breeding season remains unclear.
In three years the numbers of owls increased
considerably outside the breeding season, indicating
immigration (Fig. 7). This only occurred
in autumns and winters preceding highly
productive breeding seasons (Fig. 8). In
most years, numbers decreased during autumn
and winter (by up to 85%), due to mortality
but possibly also due to emigration. The
Netherlands are situated near the western
edge of the area in which individual Longeared
Owls track fluctuations in Microtus abundance.
I argue that communal roosting of owls
is linked to migratory populations, and that the
ultimate function is related to the possibility to
find a breeding partner.
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