Mate Choice in Captive American Kestrels, Falco sparverius, Parasitized by a Nematode, Trichinella pseudospiralis

Ethology ◽  
2010 ◽  
Vol 101 (2) ◽  
pp. 112-120 ◽  
Author(s):  
Derin Henderson ◽  
David M. Bird ◽  
Manfred E. Rau ◽  
Juan J. Negro
1988 ◽  
Vol 66 (7) ◽  
pp. 1685-1692 ◽  
Author(s):  
Michèle D. Saumier ◽  
Manfred E. Rau ◽  
David M. Bird

Trichinella pseudospiralis infections induced mild behavioural changes in the American kestrel host (Falco sparverius) within the first 5 days postinoculation, a period that corresponds to the adult phase of the infection. However, more severe effects on mobility were precipitated as the larvae migrated and became established in the musculature. The debilitation persisted for at least 5 weeks postinoculation and involved a reduction in exercising, flying, elevated perching, and preening, and was accompanied by an increase in the frequency of walking and floor perching. Such behavioural effects, attributable to the presence of muscle larvae, may reduce the competitive fitness of infected individuals. The muscle larvae were randomly distributed among various muscle groups.


1982 ◽  
Vol 60 (12) ◽  
pp. 3150-3152 ◽  
Author(s):  
E. Meerovitch ◽  
K. Chadee ◽  
D. M. Bird

Trichinella pseudospiralis Garkavi, 1972, but not T. spiralis was shown to be infective to American kestrels, Falco sparverius. A maximum of only 5.1% of the larvae administered were able to develop to the adult stage in the intestine. In vitro release of newborn larvae by female worms, recovered on days 10 and 15 postinoculation, was low. Adult worms were eliminated from the intestine by day 25 postinoculation. Few muscle larvae were first observed on day 20 postinoculation; their number increased with time but was never as high as in similarly experimentally infected mice.


1986 ◽  
Vol 64 (10) ◽  
pp. 2123-2125 ◽  
Author(s):  
Michèle D. Saumier ◽  
Manfred E. Rau ◽  
David M. Bird

Trichinella pseudospiralis infections reduced the reproductive success of captive American kestrels (Falco sparverius). Infected birds manifested a delayed onset of egg laying (day 31) when compared with uninfected controls (day 23). All control females continued to produce eggs after the first three were removed, but only 66.7% of the infected females managed to do so. Consequently, infected birds produced a mean total of only 4.9 eggs, as compared with 7.1 eggs for the controls. Breakage (29.0%) and embryo mortality (40.0%) were the major sources of egg loss among infected birds. The corresponding losses among control birds were 1.6 and 4.7%, respectively. Consequently, control birds produced an average of 2.1 hatchlings per pair, whereas infected birds produced only 0.6.


2011 ◽  
Vol 30 (11) ◽  
pp. 2570-2575 ◽  
Author(s):  
Kim J. Fernie ◽  
Sarah C. Marteinson ◽  
David M. Bird ◽  
Ian J. Ritchie ◽  
Robert J. Letcher

2018 ◽  
Vol 11 (4) ◽  
pp. 238-244 ◽  
Author(s):  
Joshua Suich ◽  
Gary Ritchison

When perched, several species of small falcons, including American Kestrels (Falco sparverius), often pump their tails, but the possible function of this behaviour is unknown. Our objective was to use observations and experiments to examine the possible function(s) of tail-pumping by American Kestrels. Fieldwork was conducted from March 2015 to December 2015 at the Blue Grass Army Depot in Madison County, Kentucky. During observations of focal kestrels, we noted their behaviour (e.g. landing on a perch, hunting, or consuming prey), including when and how often they pumped their tails (i.e. rapid movement of the tail down, then back up to its original position). Kestrels typically tail-pumped when landing on a perch (mean = 4.1±0.2 pumps per 10 s) and consuming prey (mean = 2.4±0.2 pumps per 10 s). When hunting, kestrels tail-pumped at higher rates during the 30 s prior to attacking (mean = 1.1±0.3 pumps) than they did during the 30–60 s interval before an attack (mean = 0.3±0.1 pumps). During experiments where kestrels were presented with models of a conspecific and a predator (Cooper's Hawk, Accipiter cooperi), we found no difference in rates of tail-pumping prior to and during the presentation. These results suggest that tail-pumping by American Kestrels is not used either to communicate with conspecifics or as a predator-deterrent signal. Rather, kestrels appear to tail-pump to help maintain balance on perches when landing and consuming prey. In addition, prior to attacking prey, kestrels typically bob their heads (possibly to aid in judging distances), and tail-pumping may help them maintain stability as they head-bob and prepare to attack.


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