Why pace? The influence of social, housing, management, life history, and demographic characteristics on locomotor stereotypy in zoo elephants

2017 ◽  
Vol 194 ◽  
pp. 104-111 ◽  
Author(s):  
Brian J. Greco ◽  
Cheryl L. Meehan ◽  
Jennifer L. Heinsius ◽  
Joy A. Mench
2001 ◽  
Vol 10 (4) ◽  
pp. 435-457 ◽  
Author(s):  
David Cowan ◽  
Christina Pantazis ◽  
Rose Gilroy

This article considers the ways in which social housing has in recent years become inextricably linked with the process of crime control. Drawing on case study research into the rehousing of sex offenders, the authors provide evidence illustrating why and how social housing management has become increasingly drawn into the fold of crime control. The article then highlights some serious but often neglected concerns stemming from the adoption by social housing management of more crime control responsibilities. Whilst protection of individuals and communities should always remain paramount, the article concludes with a discussion about the implications of what these processes may mean for social housing.


2014 ◽  
Vol 41 (2) ◽  
pp. 172 ◽  
Author(s):  
M. V. Vadell ◽  
I. E. Gómez Villafañe ◽  
R. Cavia

Context Life-history theory attempts to explain the way in which an organism is adapted to its environment as well as explaining the differences in life-history strategies among and within species. Aims The aim of this paper was to compare life-history traits of the Norway rat and the house mouse living in different habitats and geographic regions so as to find patterns related to environmental characteristics on the basis of published ecological studies conducted before 2011. Methods The environments where rodent populations lived were characterised according to climate type, occurrence of freezing temperatures and frost, degree of anthropisation and trapping location. Four demographic characteristics were analysed. A canonical correspondence analysis was performed to explain the effects of environmental variables on the demographic characteristics of rodents. Information was gathered from 35 articles published between 1945 and 2010. Key results Most populations of both species showed differences in abundance throughout the year, but no defined pattern was common among populations. The pregnancy rate of Norway rat was highest during spring and autumn in urban environments, during spring and winter in rural environments and during summer in sylvan habitats. House mouse populations were most frequently reported to experience high pregnancy rates during summer. Contrary to urban and rural populations, in sylvan environments the occurrence of a reproductive break was the most commonly reported pattern for both species. Litter size of Norway rat depended on the degree of anthropisation and the occurrence of freezing temperatures and frost. Litter size was greater in rural environments and in areas without freezing temperatures and frost. House mouse did not show differences in litter size resulting from any of the environmental characteristics analysed. Conclusions Both species are able to modify their reproductive strategies according to environmental characteristics, especially according to the degree of anthropisation of the environment. In sylvan areas, where animals are more exposed to seasonal changes in weather conditions, changes in reproductive investment are more evident. Implications Regarding the implications for rodent control, the best time to apply control measures could be winter in sylvan and urban environments. In rural environments, the best time for conducting control efforts is less clear, although cold seasons seem also to be the best.


2004 ◽  
Vol 22 (3) ◽  
pp. 186-188 ◽  
Author(s):  
Vincent Gruis ◽  
Nico Nieboer

2018 ◽  
pp. 108-128
Author(s):  
Richard Walker

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