Temporal and spatial variation in sex-specific abundance of the avian vampire fly (Philornis downsi)
Understanding the range and behaviour of an invasive species is critical to identify key habitat areas to focus control efforts. Patterns of range use in parasites can differ temporally, across life stages and between sexes. The invasive avian vampire fly, Philornis downsi, spends the larval stage o...
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Zusammenfassung: | Understanding the range and behaviour of an invasive species is critical
to identify key habitat areas to focus control efforts. Patterns of range
use in parasites can differ temporally, across life stages and between
sexes. The invasive avian vampire fly, Philornis downsi, spends the larval
stage of its life within bird nests, feeding on developing nestlings and
causing high levels of mortality and deformation. However, little is known
of the ecology and behaviour of the non-parasitic adult fly life stage.
Here, we document sex-specific temporal and spatial patterns of abundance
of adult avian vampire flies during a single Darwin’s finch breeding
season. We analyse fly trapping data collected across 7 weeks in the
highlands (N = 405 flies) and lowlands (N = 12 flies) of Floreana Island
(Galápagos). Lowland catches occurred later in the season, which supports
the hypothesis that flies may migrate from the food-rich highlands to the
food-poor lowlands once host breeding has commenced. Fly abundance was not
correlated with host nesting density (oviposition site) but was correlated
with distance to the agricultural zone (feeding site). We consistently
caught more males closer to the agricultural zone and more females further
away from the agricultural zone. These sex differences suggest that males
may be defending or lekking at feeding sites in the agricultural zone for
mating. This temporal and sex-specific habitat use of the avian vampire
fly is relevant for developing targeted control methods and provides
insight into the behavioural ecology of this introduced parasite on the
Galápagos Archipelago. |
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DOI: | 10.5061/dryad.3j9kd51kc |