Abstract

Molecular species identification from biological material collected at field sites has become an established ecological tool. However, extracting and amplifying DNA from degraded field samples, such as prey remains and feces that have been exposed to the elements, remains a challenge and costly. We collected 115 fecal samples of unknown small mammals, resembling fecal droppings of voles and mice (i.e., Cricetidae and Muridae), from a salt marsh in The Netherlands. We modified a previously published protocol into a relatively low-cost method with a PCR success of 95%. We demonstrate that species identification is possible for both Cricetidae and Muridae species using fecal samples of unknown age deposited in the field. For 90 samples, sequences of the variable control region in the mitochondrial genome were obtained and compared to published DNA sequences of small mammals occurring in north European salt marshes. A single sample, probably environmentally contaminated, appeared as Sus scrofa (n = 1). We positively identified house mouse Mus musculus, being the positive control (n = 1), and common vole Microtus arvalis (n = 88). In 81 sequences of 251 nt without ambiguous bases, ten haplotypes were present. These haplotypes, representing the central lineage of the western subspecies M. arvalis arvalis, were separated by 20 mutations from published control region haplotypes of the western European lineages sampled in France. Unlike earlier studies of cytochrome b variation in coastal European populations, we did not find indications of recent purging of genetic variation in our study area.

Highlights

  • Identification of taxa by molecular analysis of a variety of biological samples found in natural environments has become a well-established replacement or addition to collecting, trapping, or other invasive sampling (Höss et al 1992; BejaPereira et al 2009)

  • We successfully demonstrated that the technique for molecular species identification of voles developed by Alasaad et al (2011) can be applied to feces of voles and mice living in natural temperate habitats, and discovered ten unpublished haplotypes from the western subspecies of common vole Microtus arvalis arvalis

  • The proportion of successful PCRs increased to 51% with the modified ammoniumacetate method, and to 95% where the pre-lysis soaking time of feces was increased from 60 s to 10 min: of 76 field samples treated with 10-min pre-lysis soaking, only four PCRs failed (Table 2)

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Summary

Introduction

Identification of taxa by molecular analysis of a variety of biological samples found in natural environments has become a well-established replacement or addition to collecting, trapping, or other invasive sampling (Höss et al 1992; BejaPereira et al 2009). Species identification of many taxa is made possible by extensive, publicly available, databases such. This study aims to identify the vole and mouse species (Cricetidae and Muridae, superfamily: Muroidea) inhabiting a salt marsh in The Netherlands, from feces collected in natural habitats using molecular tools with a relatively low-cost DNA extraction method. Voles and mice deposit fecal droppings throughout their territories (Delattre et al 1996; Wheeler 2008). DNA in fecal droppings of wild free-roaming animals has been exposed

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