Abstract

Alpine marmots Marmota marmota occupy a narrow altitudinal niche within high elevation alpine environments. For animals living at such high elevations where resources are limited, parasitism represents a potential major cost in life history. Using occupancy models, we tested if marmots living at higher elevation have a reduced risk of being infected with gastro-intestinal helminths, possibly compensating the lower availability of resources (shorter feeding season, longer snow cover and lower temperature) than marmots inhabiting lower elevations. Detection probability of eggs and oncospheres of two gastro-intestinal helminthic parasites, Ascaris laevis and Ctenotaenia marmotae, sampled in marmot feces, was used as a proxy of parasite abundance. As predicted, the models showed a negative relationship between elevation and parasite detectability (i.e. abundance) for both species, while there appeared to be a negative effect of solar radiance only for C. marmotae. Site-occupancy models are used here for the first time to model the constrains of gastrointestinal parasitism on a wild species and the relationship existing between endoparasites and environmental factors in a population of free-living animals. The results of this study suggest the future use of site-occupancy models as a viable tool to account for parasite imperfect detection in eco-parasitological studies, and give useful insights to further investigate the hypothesis of the contribution of parasite infection in constraining the altitudinal niche of Alpine marmots.

Highlights

  • Parasite infections are costly to their hosts: the development and maintenance of antiparasitic defenses competes for resources with other life-history functions, such as reproduction, growth, and development of secondary sexual traits [1,2,3,4]

  • Oncospheres and/or proglottids of C. marmotae were detected in 274/587 specimens

  • C. marmotae was first detected at the end of May (May 22nd), in five fecal specimens from the sampling sites located at the lowest elevation

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Summary

Introduction

Parasite infections are costly to their hosts: the development and maintenance of antiparasitic defenses competes for resources with other life-history functions, such as reproduction, growth, and development of secondary sexual traits [1,2,3,4]. While there are many studies and examples of tradeoffs between behavioral and life history traits and parasite resistance in wild populations [9, 10, 11], only few studies have investigated the potential role such a tradeoff could have in constraining the distributional niche of wildlife populations to areas in which the cost of the risk of parasite infection is below the cost of maintaining antiparasitic strategies [12, 13, 14]

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