|
|
Rubenstein D.I. (2015). Networks of terrestrial ungulates: linking form and function. In D. P. & Croft D. W. Franks R. James J. Krause (Ed.), Animal Social Networks. Oxford: Oxford University Press.
|
|
|
|
Rubenstein Di,. (1981). Behavioural ecology of island feral horeses. Equine. Vet. J., 13, 27–34.
|
|
|
|
Rubenstein Di,. (1978). Islands and their effects on the social organization of feral horses. ABS Symp, .
|
|
|
|
Rubenstein, D. (2015). Social Networks: Linking Form with Function in Equid Societies. In K. Krueger (Ed.), Proceedings of the 3. International Equine Science Meeting. Proc. 3. Int. Equine. Sci. Mtg, in prep. Wald: Xenophon Publishing.
Abstract: Animal societies develop from interactions and relationships that occur among individuals within populations. The fundamental tenet of behavioral ecology is that ecological factors shape behavior and determine the distribution and associations of individuals on landscapes. As a result, different social systems emerge in different habitats and under different environmental conditions. Since characterizing social systems depends on time and motion studies of individual actions and interactions that are often bilateral, such characterizations are often coarse-grained. If social relationships can be characterized using social networks, however, seemingly similar social organizations often reveal informative differences in terms of deep structure. Thus social network theory should be able to provide insights in to the connections between social form and function. This talk will explore how the network structures of horses, zebras and asses can provide novel insights into the functioning of animal societies with respect to the spread of memes, genes and diseases.
|
|
|
|
Rubenstein, D. (2012). Wild Equid Movements: Impacts of Habitat Quality, Predation Pressure and Leadership. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Animals spend much of their lives on the move searching for food, shelter and mates. As long-legged, large bodied species, equids are well suited for traveling long distances. Understanding where free-ranging equids go, why they choose particular locations, some near and some far, and what impact such movements have on patterns of sociality, demography and human livelihoods are only now coming into focus. This talk will explore how bottom-up factors, such as the abundance and distribution of key resources, and top-down factors, such as the type and location of predators, interact to shape overall movement patterns of equids, how leadership roles develop and what outcomes such movements are likely to have on human activities.
|
|
|
|
Rubenstein, D. I. (1994). The ecology of female social behaviour in horses, zebras and asses. In P. J. Jarman, & A. R. (Eds.), Animal Societies (pp. 13–28). Kyoto University Press.
|
|
|
|
Rubenstein, D. I.,. (1986). Ecology and sociality in horses and zebras. In D. I. Rubenstein, & R. W. Wrangham (Eds.), Ecological Aspects of Social Evolution (pp. 282–302). Princeton, NJ.: Princeton University Press.
|
|
|
|
Rubenstein, D. I., & Hack, M. A. (1992). Horse signals: The sounds and scents of fury. Evol. Ecol., 6(3), 254–260.
Abstract: During contests animals typically exchange information about fighting ability. Among feral horses these signals involve olfactory or acoustical elements and each type can effectively terminate contests before physical contact becomes necessary. Dung transplant experiments show that for stallions, irrespective of rank, olfactory signals such as dung sniffing encode information about familiarity suggesting that such signals can be used as signatures. As such they can provide indirect information about fighting ability as long as opponents associate identity with past performance. Play-back experiments, however, show that vocalizations, such as squeals, directly provide information about status regardless of stallion familiarity. Sonographs reveal that squeals of dominants are longer than those of subordinates and that only those of dominants have at their onset high-frequency components.
|
|
|
|
Rubenstein, D. I. (1989). Life history and social organization in arid adapted ungulates. J. Arid. Environ., 17, 145–156.
|
|
|
|
Rubenstein, D. I., & Hohmann, M. E. (1989). Parasites and Social Behavior of Island Feral Horses. Oikos, 3, 312–320.
Abstract: The horses of Shackelford Banks, North Carolina, USA, are heavily parasitized by intestinal worms and harassed by dipterans, and although both types influence behavior only internal parasites affect bodily condition and the structuring of horse society. Thirteen species of internal parasites were identified, but only 4 of 13 groups contain them all and even within groups differences among individuals are large. Among individuals ova emissions vary ranging from 50 to 76,875 eggs per gram. The most important environmental factors influencing egg production are season and a group's location on the island, presumably because of salinity and soil differences and their effects on ova survival. Of the social and life history factors, age, and group size, but neither reproductive state nor dominance status are important. The fitness consequences of internal parasitism may be large since the number emitted is negatively correlated with next year's bodily condition. Biting fly burdens are also affected by a variety of environmental factors. In general, horses are covered with more flies on sunny days, when winds are moderately brisk, when occupying dunes, and around mid-day. In contrast to endoparasites, fly burden is affected by reproductive condition and dominance status and tends to decrease as groups increase in size. Since groups do not grow very large, nor do females attempt to bring groups together, the negative effects of endoparasites appear to overide those associated with ectoparasites. Consequently, endoparasites appear to exert a stronger influence on social structure, even though ectoparasites seem to play a stronger role in shaping details of behavior.
|
|
