Five adult male Jaguars and a translocated subadult female Jaguar were captured and followed by radio-telemetry in Cockscomb Basin, Belize. One adult male Jaguar, two resident female Jaguars, and a Puma were followed only by their tracks. Radio-collared males maintained overlapping ranges of 28–40 km2, while resident females moved in minimum areas of 10 km2 within the ranges of individual males. Despite range overlap, evidence of aggression or sign of more than one large cat in the same area simultaneously was uncommon. Such avoidance behaviour suggested some means of communication. Visual marking in the form of faeces and scrapes were found uncovered along roads and trails in areas of overlap between the cats; such marking could have helped in boundary delineation as well as spatial and temporal positioning. Males often remained in small areas of 2·5 km2 for up to two weeks, a behaviour made possible by abundant prey. This behaviour may have facilitated avoidance with other Jaguars. Faecal analysis indicated opportunistic feeding on 17 prey species. Armadillo, Paca and brocket deer accounted for 94% of the available terrestrial prey and comprised 70% of the identified prey in the faeces. All Jaguars were primarily nocturnal, though activity varied between animals. The translocated female showed changes in activity patterns when feeding upon cattle. At least one Puma travelled within the ranges of several male Jaguars and appeared to be feeding on smaller prey items. The behavioural and ecological plasticity exhibited by the Jaguars in this study is beneficial for an animal whose habitat is rapidly diminishing.
[1]
J. Seidensticker.
On the Ecological Separation between Tigers and Leopards
,
1976
.
[2]
J. R. Bider.
Dynamics and the Tempro‐Spatial Relations of a Vertebrate Community
,
1962
.
[3]
Roger P Johnson,et al.
Scent marking in mammals
,
1973
.
[4]
J. Layne,et al.
Home Range of the Armadillo in Florida
,
1977
.
[5]
T. Hemker,et al.
Cougar food habits in southern Utah
,
1984
.
[6]
N. Smythe.
The natural history of the Central American agouti (Dasyprocta punctata)
,
1978
.
[7]
C. O. Mohr,et al.
Table of equivalent populations of North American small mammals
,
1947
.
[8]
E. Charnov,et al.
Ecological Implications of Resource Depression
,
1976,
The American Naturalist.
[9]
M. Hornocker.
WINTER TERRITORIALITY IN MOUNTAIN LIONS
,
1969
.
[10]
M. Sunquist,et al.
The Social Organization of Tigers (Panthera Tigris) in Royal Chitawan National Park, Nepal
,
1981
.
[11]
A. Rabinowitz.
Jaguar predation on domestic livestock in Belize.
,
1986
.
[12]
M. Hornocker,et al.
Analysis of mountain lion predation upon mule deer and elk in the Idaho Primitive area
,
1967
.
[13]
G. Schaller,et al.
Movement Patterns of Jaguar
,
1980
.
[14]
J. Anderson,et al.
Age determination of the African lion (Panthera leo)
,
2009
.
[15]
J. Eisenberg,et al.
An ecological reconnaissance of Wilpattu National Park, Ceylon
,
1972
.
[16]
G. Schaller,et al.
Jaguar predation on capybara
,
1977
.