scholarly journals Home range, sleeping site use, and band fissioning in hamadryas baboons: Improved estimates using GPS collars

Author(s):  
Megan C. Henriquez ◽  
Alexis Amann ◽  
Dawn Zimmerman ◽  
Carlos Sanchez ◽  
Suzan Murray ◽  
...  
2007 ◽  
Vol 69 (3) ◽  
pp. 325-335 ◽  
Author(s):  
Samuel P. Franklin ◽  
Sarah J. Hankerson ◽  
Andrew J. Baker ◽  
James M. Dietz

2009 ◽  
Vol 87 (3) ◽  
pp. 273-283 ◽  
Author(s):  
Kim G. Poole ◽  
Kari Stuart-Smith ◽  
Irene E. Teske

As with many ungulates inhabiting areas with potentially deep snow, winter is an important season for mountain goats ( Oreamnos americanus (de Blainville, 1816)) and is characterized by restricted movements and high juvenile mortality. We examined winter habitat selection and wintering strategies by mountain goats in two adjacent areas of southeastern British Columbia characterized by deep, moist snow and by shallow, dry snow. Fifteen GPS collars were placed on mountain goats in each area over two winters. Winter-range size did not differ between areas and comprised, on average, 2.2%–7.4% of male home range and 8.0%–14.1% of female home range. Topographic variables dominated habitat model selection. At the broad scale, mountain goats in both areas selected winter ranges closer to escape terrain on warmer aspects that contained lesser amounts of mature dense forest. At the fine scale, mountain goats in both areas selected rugged habitat at upper mid-elevations and on warmer aspects. Alpine areas were avoided in the deep snow area and selected in the shallow snow area. No selection for mature forests was observed in either area. Mountain goats, therefore, appeared to utilize open, high-elevation habitats in shallow snow zones, but they did not seek reduced snow levels in mature forest stands in deep snow areas.


2011 ◽  
Vol 57 (3) ◽  
pp. 260-268 ◽  
Author(s):  
Dayong Li ◽  
Qihai Zhou ◽  
Xiaoping Tang ◽  
Henglian Huang ◽  
Chengming Huang

Abstract We collected data on sleeping site use from two groups of white-headed langurs Trachypithecus leucocephalus living in Fusui Nature Reserve, China between August 2007 and July 2008. This information was used to test several hypotheses regarding ultimate causes of sleeping site use in this primate. White-headed langurs slept either in caves (17 sites) or on a cliff ledge (one site). They used all sleeping sites repeatedly, and reused some of them on consecutive nights; three nights was the longest consecutive use of any one sleep site. We suggest that langurs use sleeping sites to make approach and attack by predators difficult, and to increase their own familiarity with a location so as to improve chances for escape. Langurs’ cryptic behaviors with an increased level of vigilance before entering sleeping sites may also help in decreasing the possibility of detection by predators. Group 1 spent more sleeping nights in the central area of their territory than expected; in contrast, group 2 spent more sleeping nights in the periphery of their territory, which overlaps with that of another groups, than expected. The position of sleeping site relative to the last feeding site of the day and the first feeding site of the subsequent morning indicated a strategy closer to that of a multiple central place forager than of a central place forager. These results suggest that territory defense and food access may play an important role in sleeping site use of white-headed langurs.


2009 ◽  
Vol 30 (2) ◽  
pp. 353-365 ◽  
Author(s):  
Zhou Qihai ◽  
Huang Chengming ◽  
Li Ming ◽  
Wei Fuwen

2014 ◽  
Vol 41 (3) ◽  
pp. 258 ◽  
Author(s):  
Matt Amos ◽  
Greg Baxter ◽  
Neal Finch ◽  
Peter Murray

Context Wild deer are increasing worldwide and, in Australia, prompting land managers to review management strategies. Management activities may be ineffective without a sound understanding of the ecology of the species. No peer-reviewed research has been published for wild red deer in Australia, where they have been introduced. Aims To help land managers gain an understanding of some movement parameters of introduced wild red deer out of their natural range. Methods GPS collars were used to obtain movement rates (m h–1), annual home range using three estimators and seasonal home range using the Local Convex Hull estimator. Key findings Deer at our study site displayed typical crepuscular movements. However, the lack of elevated activity for stags in summer varies greatly to reports from overseas. The annual home range of hinds was much smaller than that of stags. Large differences for seasonal home ranges from the same deer for two winters suggest that seasonal conditions may exert a large influence on the size of home ranges. The home ranges of deer at our study site were comparable with the largest reported in European studies, but the relationship between deer density and home-range area was markedly different. Conclusions It appears that Australian wild red deer behave differently from their European conspecifics for several important movement parameters. Wild stags did not display the high levels of movement activity in summer, like those in Europe, and the home-range areas of our deer were very large for the high densities we encountered compared with overseas reports. Implications Targeted management of hinds may prove beneficial as hinds had a much smaller and continuous home range than stags. If managers want to target stags, there is only a short rut period when they continually associate with hinds and that may be the most efficacious time for control. Additionally, future research may need to explore the link between home range and deer density, and the effect of variation in rainfall on home range and movement of wild red deer which may influence management activities more than do the regular seasonal patterns found in Europe.


2000 ◽  
Vol 81 (3) ◽  
pp. 798-809 ◽  
Author(s):  
I. K. Hanski ◽  
P. C. Stevens ◽  
P. Ihalempia ◽  
V. Selonen

2014 ◽  
Vol 128 (3) ◽  
pp. 223 ◽  
Author(s):  
Karen Graham ◽  
Gordon B. Stenhouse

An understanding of the natural history of the Grizzly Bear (Ursus arctos) is important for recovery planning. We present data on home range size, movements and denning chronology collected using Global Positioning System (GPS) collars on Grizzly Bears in west-central Alberta. Mean annual kernel estimates for adult (1034 ± 656 (SD) km2) and subadult (1298 ± 1207 km2) males were larger than those for females with cubs of the year (213 ± 212 km2) and lone adult females (337 ± 176 km2) but not different from sub-adult females, females with yearlings, or females with ≥ 2-yr old cubs (P > 0.05). Mean rates of movement among female age–reproductive classes were different from each other (Z9 < 2.70, P > 0.05) but not different from sub-adult males (Z9 < 2.70, P > 0.05). Rates of movement of adult males were significantly different only from those of females with cubs of the year (Z9 = 3.94, P = 0.001). The greatest amount of movement occurred in June and the least in October. Bears traveled fastest in the morning and evening and slowest at night. Pregnant females had the longest denning period (175 days, ± 16 days SD). No difference was detected in denning duration among the remaining five age–sex–reproductive classes (P > 0.05). GPS collars provided large location datasets from which accurate home range estimates, hourly movement rates, and precise denning dates were determined. Examining similarities and differences in the basic biology of Grizzly Bears from various locations will improve our understanding of the plasticity of this species and the potential impacts of habitat and climate change.


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