Abstract
The maritime shrew, Sorex maritimensis, is a Canadian endemic species with a limited distribution in two provinces in eastern Canada. Phylogeographic analysis of mitochondrial DNA control region and cytochrome b sequences revealed two clades, one found in New Brunswick and the other primarily in Nova Scotia, Canada. We propose that these clades have come back into secondary contact following the Wisconsin glaciation via wetlands on the narrow Isthmus of Chigneto that connects these provinces. Despite evidence of an historic separation of maritime shrew subpopulations in Nova Scotia and New Brunswick, we conclude that shrews in these two regions should be considered a single evolutionary significant unit but separate, semi-isolated management units that should be recognized as such for conservation purposes. The susceptibility of this stenotopic species with limited dispersal capabilities raises concerns about its long-term persistence if climate-change induced habitat fragmentation increases. Maintenance of contiguous wetland habitats is needed to ensure connectivity and gene flow among populations of the maritime shrew.
Similar content being viewed by others
References
Bannikova AA, Lavrenchenko LA, Kramerov DA (2005) Phylogenetic relationships between Afrotropical and Palaearctic Crocidura species inferred from inter-SINE-PCR. Biochem Syst Ecol 33:45–59. doi:10.1016/j.bse.2004.05.014
Borodulina OR, Kramerov DA (2001) Short interspersed elements (SINEs) from insectivores Two classes of mammalian SINEs distinguished by A-rich tail structure. Mamm Genome 12:779–786. doi:10.1007/s003350020029
Crandall KA, Bininda-Emonds ORP, Mace GM, Wayne RK (2000) Considering evolutionary processes in conservation biology. Trends Ecol Evol 17:390–395
Dawe KL (2005) Habitat associations and genetic diversity of the maritime shrew, Sorex maritimensis. MSc Thesis, Acadia University
Dubey S, Cosson J-F, Vohralik V, Krystufek B, Diker E, Vogel P (2007) Molecular evidence of Pleistocene bidirectional fauna exchange between Europe and the Near East: the case of the bicoloured shrew (Crocidura leucodon, Soricidae). J Evol Biol 20:1799–1808. doi:10.1111/j.1420-9101.2007.01382.x
Excoffier L, Smouse PE, Quattro JM (1992) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131:479–491
Fumagalli L, Taberlet P, Stewart DT, Gielly L, Hausser J, Vogel P (1999) Molecular phylogeny and evolution of Sorex shrews (Soricidae: Insectivora) inferred from mtDNA sequence data. Mol Phylogenet Evol 11:222–235. doi:10.1006/mpev.1998.0568
Gannon WL, Sikes RS, the Animal Care, Use Committee of the American Society of Mammalogists (2007) Guidelines of the American Society of mammalogists for the use of wild mammals in research. J Mammal 88:809–823. doi:10.1644/06-MAMM-F-185R1.1
Grant WS, Bowen BW (1998) Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. J Hered 89:415–426. doi:10.1093/jhered/89.5.415
Herman TB, Scott FW (1992) Global change at the local level: assessing the vulnerability of vertebrate species to climatic warming. In: Willison JHM, Bondrup-Nielsen S, Drysdale C, Herman TB, Munro NWP, Pollock TL (eds) Science and the management of protected areas. Elsevier, New York, pp 353–367
Irwin DM, Kocher TD, Wilson AC (1991) Evolution of the cytochrome b gene of mammals. J Mol Evol 32:128–144. doi:10.1007/BF02515385
Kocher TD, Thomas WK, Meyer A, Edwards SV, Paabo S, Villablanca FX et al (1989) Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci USA 86:6196–6200. doi:10.1073/pnas.86.16.6196
McCarthy C (1996) Chromas 1.45. School of Health Science. Griffith University, Southport, Queensland
Mockford SW, Herman TB, Snyder M, Wright JM (2007) Conservation genetics of Blanding’s turtle and its application in the identification of evolutionarily significant units. Conserv Genet 8:209–218. doi:10.1007/s10592-006-9163-4
Moritz C (1994a) Applications of mitochondrial DNA analysis in conservation: a critical review. Mol Ecol 3:401–411. doi:10.1111/j.1365-294X.1994.tb00080.x
Moritz C (1994b) Defining ‘evolutionary significant units’ for conservation. Trends Ecol Evol 9:373–375. doi:10.1016/0169-5347(94)90057-4
Nagorsen D (2004) Canada’s endemic mammals at risk: recent taxonomic advances and priorities for conservation. In: Hooper TD (ed) Proceedings of the Species at Risk 2004 Pathways to Recovery Conference March 2–6, 2004, Victoria, British Columbia. Species at Risk 2004 Pathways to Recovery Conference Organizing Committee, Victoria, British Columbia, p 2
Pearce JM (2006) Minding the gap: frequency of indels in mtDNA control region sequence data and influence on population genetic analysis. Mol Ecol 15:333–341. doi:10.1111/j.1365-294X.2005.02781.x
Peltonen A, Hanski I (1991) Patterns of island occupancy explained by colonization and extinction rates in shrews. Ecology 72:1698–1708. doi:10.2307/1940969
Petersen SD, Stewart DT (2006) Biogeography and conservation genetics of southern flying squirrels, Glaucomys volans, from Nova Scotia. J Mammal 87:153–160. doi:10.1644/05-MAMM-A-062R1.1
Posada D (2007) version 1.2. available from http://darwin.uvigo.es
Posada D, Crandall KA (1998) Modeltest: testing the model of DNA substitution. Bioinformatics 14:817–818. doi:10.1093/bioinformatics/14.9.817
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959
Province of Nova Scotia (1994) Glaciation, deglaciation and sea-level changes. In: Natural History of Nova Scotia. Nova Scotia Museum of Natural History, vol 1. Halifax, Nova Scotia, pp 57–64
Rambaut A (1996) Se-Al: Sequence Alignment Editor. Available at http://evolve.zoo.ox.ac.uk
Ryder OA (1986) Species conservation and systematics: the dilemma of subspecies. Trends Ecol Evol 1:9–10. doi:10.1016/0169-5347(86)90059-5
Schneider S, Roessli D, Excoffier L (2000) Arlequin ver. 2.000: a software package for population genetics data analysis. Genetics and Biometry Laboratory, University of Geneva, Switzerland
Shafer ABA, Stewart DT (2007) Phylogenetic relationships among Nearctic shrews of the genus Sorex (Insectivora, Soricidae) inferred from combined cytochrome b and inter-SINE fingerprint data using Bayesian analysis. Mol Phylogenet Evol 44:192–203. doi:10.1016/j.ympev.2006.12.003
Sipe TW, Browne RA (2004) Phylogeography of masked shrews (Sorex cinereus) and smoky shrews (Sorex fumeus) in the Southern Appalachians. J Mammal 85:875–885. doi:10.1644/214
Stewart DT, Baker AJ (1992) Genetic differentiation and biogeography of the masked shrew in Atlantic Canada. Can J Zool 70:106–114
Stewart DT, Baker AJ (1994) Patterns of sequence variation in the mitochondrial D-loop region of shrews. Mol Biol Evol 11:9–21
Stewart DT, Baker AJ (1997) A phylogeny of some taxa of masked shrews (Sorex cinereus) based on mitochondrial DNA D-loop sequences. J Mammal 78:361–376. doi:10.2307/1382890
Stewart DT, Perry ND, Fumagalli L (2002) The maritime shrew, Sorex maritimensis (Insectivora: Soricidae): a newly recognized Canadian endemic. Can J Zool 80:94–99. doi:10.1139/z01-207
Swofford DL (2003) PAUP*: phylogenetic analysis using parsimony (* and other methods). Sinauer Associates, Sunderland, Massachusetts
van Zyll de Jong CG (1983a) A morphometric analysis of North American shrews of the Sorex arcticus group, with special consideration of the taxonomic status of S. a. maritimensis. Nat Can 110:373–378
van Zyll de Jong CG (1983b) Handbook of Canadian Mammals. vol 1. Marsupials and Insectivores. National Museums of Canada, Ottawa
Volobouev VT, Van Zyll De Jong CG (1988) The karyotype of Sorex arcticus maritimensis (Insectivora, Soricidae) and its systematic implications. Can J Zool 66:1968–1972
Wilson DE, Reeder DM (2005) Mammal species of the world: a taxonomic and geographic reference. The Johns Hopkins University Press, Baltimore
Acknowledgements
We are grateful for in-kind support from Colin McKinnon of the Canadian Wildlife Service, Eric Tremblay of Kouchibouguac National Park, and Joe Kennedy of the New Brunswick Department of Natural Resources and Energy (Hampton). We also thank Margaret Wheaton and the many landowners for the use of their property. Julie Read, Patrick McCamphill, Owen Thompson, and Roxanne Struk provided great field and lab assistance and Sara Good-Avila offered helpful statistical advice. Funding for this project came from a Nova Scotia Museum Rare Species Grant, the Nova Scotia Habitat Conservation Fund, the New Brunswick Wildlife Trust Fund, and a National Sciences and Engineering Research Council of Canada Discovery Grant to DTS. KLD was supported by Acadia University Teaching Fellowships, the IUGB Wildlife Research Award, the Margaret McCarthy Research Scholarship, and the New Brunswick Museum Florence M. Christie Research Fellowship in Zoology.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Dawe, K.L., Shafer, A.B.A., Herman, T.B. et al. Diffusion of nuclear and mitochondrial genes across a zone of secondary contact in the maritime shrew, Sorex maritimensis: implications for the conservation of a Canadian endemic mammal. Conserv Genet 10, 851–857 (2009). https://doi.org/10.1007/s10592-008-9645-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10592-008-9645-7