Sexually dimorphic eggs, nestling growth and sibling competition in American Kestrels Falco sparverius

1997 ◽  
Vol 11 (3) ◽  
pp. 331-335 ◽  
Author(s):  
D. J. ANDERSON ◽  
J. REEVE ◽  
D. M. BIRD
1985 ◽  
Vol 63 (11) ◽  
pp. 2590-2593 ◽  
Author(s):  
Reed Bowman ◽  
David M. Bird

Egg dimensions, nestling growth, and reproductive success were compared between first and second clutch nests of American Kestrels (Falco sparverius) to determine the influence of renesting on fledging success. Eggs were removed from 11 nests during 1982–1983. Eight nests served as controls. Most pairs (81.8%) renested on their original territory. We found no significant differences in egg dimensions, fertility, or hatchability between the two groups. Second clutch males (n = 6 clutches) were smaller at hatching than males from first clutches (n = 8 clutches). By day 24 these males (n = 5 clutches) were heavier, with significantly longer manus and antebrachia than first clutch males (n = 3 clutches). However, five of eight first clutch nests fledged all males before day 24. Males remaining in first clutch nests beyond day 24 were lighter with significantly smaller antebrachia by day 18 than males fledging before day 24. This may have biased our comparisons between first and second clutch males. No significant differences in growth were found between female groups. First-clutch progeny fledged significantly younger than second-clutch birds. Males fledged earlier than females in first clutches, but the sexes fledged simultaneously in second clutches.


1992 ◽  
Vol 70 (12) ◽  
pp. 2421-2425 ◽  
Author(s):  
Nicholas W. Gard ◽  
David M. Bird

To study factors regulating clutch size in American Kestrels (Falco sparverius), brood manipulation experiments were performed on captive and wild birds in southwestern Quebec during 1986 and 1987. The largest normally occurring brood size was 5 young. Manipulations enlarged or decreased broods to 7 or 2 young, respectively. Significantly more young fledged from wild control and enlarged broods in 1987 than from comparable groups in 1986. The average number of young fledging from enlarged wild broods in 1987 was slightly higher than for control broods, but fledging weight was significantly depressed in enlarged broods. Growth rates and tarsal and antebrachial length at fledging were not affected by brood size, but development of primary feathers was slower in enlarged wild broods. Parental ability to adequately feed all young appears to be the major factor limiting brood size in American Kestrels.


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

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.


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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