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Genetic differentiation and postglacial migration of the Dactylorhiza majalis ssp. traunsteineri/lapponica complex into Fennoscandia

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Abstract

Eight variable regions (microsatellites, insertion/deletion and duplication regions) from the plastid DNA genome were analyzed for 91 populations belonging to Dactylorhiza majalis ssp. traunsteineri and closely related taxa. A total of 36 composite plastid haplotypes were found. The two dominating haplotypes had a clear geographic distribution suggesting at least two separate immigration routes into Scandinavia after the last glaciation: one southwestern route and one or two southeastern routes. D. majalis ssp. traunsteineri could not be clearly separated from any of the other taxa included in the study except for D. majalis ssp. sphagnicola. The morphologically similar taxa D. majalis ssp. traunsteineri, D. majalis ssp. lapponica and D. majalis ssp. russowii showed no genetic differentiation, and therefore we suggest an amalgamation of the three taxa into one broadly circumscribed subspecies; D. majalis ssp. lapponica. The plastid data also revealed incidents of hybridization and possible introgression between D. majalis ssp. lapponica and other members of the genus, e.g., D. incarnata.

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References

  • Aagaard SMD, Sastad SM, Greilhuber J, Moen AA (2005) Secondary hybrid zone between diploid Dactylorhiza incarnata ssp cruenta and allotetraploid D. lapponica (Orchidaceae). Heredity 94:488–496

    Article  PubMed  CAS  Google Scholar 

  • Adams JM (1997) Global land environments since the last interglacial. Oak Ridge National Laboratory, TN. http://www.esd.ornl.gov/ern/qen/nerc.html

  • Adams JM, Faure H (eds) (1997) QEN members. Review and atlas of palaeovegetation: preliminary land ecosystem maps of the world since the last glacial maximum. Oak Ridge National Laboratory, TN. http://www.esd.ornl.gov/ern/qen/adams1.html

  • Andersson E (1994) On the identity of orchid populations: a morphometric study of the Dactylorhiza traunsteineri complex in eastern Sweden. Nord J Bot 14:269–275

    Article  Google Scholar 

  • Andersson E (1995) Age-related morphological differentiation among populations of Dactylorhiza traunsteineri (Orchidaceae) in eastern Sweden. Nord J Bot 15:127–137

    Article  Google Scholar 

  • Andersson E (1996) Morphological variation in the orchid Dactylorhiza traunsteineri. Scale and systematic implications. Doctoral dissertation, Uppsala University, Uppsala

  • Bandelt H-J, Forster P, Röhl A (1999) Median-joining networks for inferring intraspecific phylogenies. Molec Biol Evol 16:37–48. http://www.fluxus-engineering.com

    Google Scholar 

  • Baumann H, Künkele S (1988) Die Orchideen Europas. Kosmos Naturführer, Stuttgart

    Google Scholar 

  • Baumann H, Künkele S, Lorenz R (2006) Orchideen Europas. Mit angrenzenden Gebieten. Ulmer Naturführer, Stuttgart

    Google Scholar 

  • Berglund M (2004) Holocene shore displacement and chronology in Ångermanland, eastern Sweden, the Scandinavian glacio-isostatic uplift centre. Boreas 33:48–60

    Article  Google Scholar 

  • Berglund AN, Westerbergh A (2001) Two postglacial immigration lineages of the polyploid Cerastium alpinum (Caryophyllaceae). Hereditas 134:171–183

    Article  PubMed  CAS  Google Scholar 

  • Bjurulf P (2005) Morphological variation in Dactylorhiza majalis ssp. sphagnicola and ssp. traunsteineri in different habitats. Svensk Bot Tidskr 99:124–132

    Google Scholar 

  • Borgen L, Hultgård UM (2003) Parnassia palustris: a genetically diverse species in Scandinavia. Bot J Linn Soc 142:347–372

    Article  Google Scholar 

  • Brochmann C, Brysting AK, Alsos IG, Borgen L, Grundt HH, Scheen A-C, Elven R (2004) Polyploidy in arctic plants. Biol J Linn Soc 82:521–536

    Article  Google Scholar 

  • Cafasso D, Widmer A, Cozzolino S (2005) Chloroplast DNA inheritance in the orchid Anacamptis palustris using single-seed polymerase chain reaction. Heredity 96(1):66–70

    CAS  Google Scholar 

  • Chase MW, Hills HG (1991) Silica gel: an ideal material for field preservation of leaf samples for DNA studies. Taxon 40:215–220

    Article  Google Scholar 

  • Corriveau JL, Coleman AW (1988) Rapid screening method to detect potential biparental inheritance of plastid DNA and results for over 200 angiosperm species. Amer J Bot 75(10):1443–1458

    Article  Google Scholar 

  • Cozzolino S, Cafasso D, Pellegrino G, Musacchio A, Widmer A (2003) Fine-scale phylogeographical analysis of Mediterranean Anacamptis palustris (Orchidaceae) populations based on chloroplast minisatellite and microsatellite variation. Molec Ecol 12:2783–2792

    Article  CAS  Google Scholar 

  • Delforge P (1995) Orchids of Britain and Europe. Harper Collins Publishers, London

    Google Scholar 

  • Delforge P (2001) Guide des Orchidées d′Europe, d′Afrique du Nord et du Proche-Orient. Delachaux et Niestlé, Lausanne

    Google Scholar 

  • Demesure B, Sodzi N, Petit RJ (1995) A set of universal primers for amplification of polymorphic non-coding regions of mitochondrial and chloroplast DNA in plants. Molec Ecol 4:129–131

    Article  CAS  Google Scholar 

  • de Soó R (1980) Dactylorhiza. In: Tutin TG et al. (eds) Flora Europea 5. Cambridge University Press, Cambridge, pp 333–337

    Google Scholar 

  • Devos N, Tyteca D, Raspé O, Wesselingh RA, Jacquemart A-L (2003) Patterns of chloroplast diversity among western European Dactylorhiza species (Orchidaceae). Pl Syst Evol 243:85–97

    Article  CAS  Google Scholar 

  • Devos N, Raspé O, Oh S-H, Tyteca D, Jacquemart A-L (2006) The evolution of Dactylorhiza (Orchidaceae) allotetraploid complex: insights from nrDNA sequences and cpDNA PCR-RFLP data. Molec Phylogenet Evol 38:767–778

    Article  PubMed  CAS  Google Scholar 

  • Doyle JJ, Doyle JH (1990) Isolation of plant DNA from fresh tissue. Focus 12:13–15

    Google Scholar 

  • Dressler RL (1993) Phylogeny and classification of the orchid family. Cambridge University Press, Cambridge

    Google Scholar 

  • Ekman S (1985) Dactylorhiza sphagnicola and D. traunsteineri with unspotted leaves found in E Uppland. Svensk Bot Tidskr 79:85–91

    Google Scholar 

  • Excoffier L, Laval G, Schneider S (2005) Arlequin ver. 3.0: an integrated software package for population genetics data analysis. Evolutionary Bioinformatics Online 1:47–50

    CAS  Google Scholar 

  • Ferris C, King RA, Väinölä R, Hewitt GM (1998) Chloroplast DNA recognizes three refugial sources of European oaks and suggests independent eastern and western immigrations to Finland. Heredity 80:584–593

    Article  PubMed  Google Scholar 

  • Grant V (1981) Plant speciation. Colombia University press, New York

    Google Scholar 

  • Hansson S (1994) A study of Dactylorhiza lapponica. Svensk Bot Tidskr 88:17–28

    Google Scholar 

  • Hedrén M (1996) Genetic differentiation, polyploidization and hybridization in northern European Dactylorhiza (Orchidaceae): evidence from allozyme markers. Pl Syst Evol 201:31–55

    Article  Google Scholar 

  • Hedrén M (2003) Plastid DNA variation in the Dactylorhiza incarnata/maculata polyploid complex and the origin of allotetraploid D. sphagnicola (Orchidaceae). Molec Ecol 12:2669–2680

    Article  Google Scholar 

  • Hedrén M, Fay MF, Chase MW (2001) Amplified fragment length polymorphisms (AFLP) reveal details of polyploid evolution in Dactylorhiza (Orchidaceae). Amer J Bot 88:1868–1880

    Article  Google Scholar 

  • Hedrén M, Nordström S, Hovmalm HAP, Pedersen HÆ, Hansson S (2007) Patterns of polyploid evolution in Greek marsh orchids (Dactylorhiza; Orchidaceae) as revealed by allozymes, AFLPs, and plastid DNA data. Amer J Bot 94:1205–1218

    Article  Google Scholar 

  • Heslop-Harrison J (1954) A synopsis of the dactylorchids of the British Isles. Berichte des Geobotanischen Forschungsinstituts Rübel 1953:53–82

    Google Scholar 

  • Hewitt G (1996) Some genetic consequences of ice ages, and their role in divergence and speciation. Biol J Linn Soc 58:247–276

    Google Scholar 

  • Hultén E (1950) Atlas of the distribution of vascular plants in NW Europe. Generalstabens litografiska anstalts förlag, Stockholm

    Google Scholar 

  • Hylander N (1966) Nordisk kärlväxtflora II. Almquist och Wiksell, Stockholm

    Google Scholar 

  • Jaarola M, Tegelström H (1995) Colonization history of north European field voles (Microtus agrestis) revealed by mitochondrial DNA. Molec Ecol 4:299–310

    Article  CAS  Google Scholar 

  • Jersáková J, Malinová T (2007) Spatial aspects of seed dispersal and seedling recruitment in orchids. New Phytol 176:448–459

    Article  Google Scholar 

  • Jordan WC, Courtney MW, Neigel JE (1996) Low levels of intraspecific genetic variation at a rapidly evolving chloroplast DNA locus in North American duckweeds (Lemnaceae). Amer J Bot 83:430–439

    Article  CAS  Google Scholar 

  • King RA, Ferris C (1998) Chloroplast DNA phylogeography of Alnus glutinosa (L) Gaertn. Molec Ecol 7:1151–1162

    Article  CAS  Google Scholar 

  • Krok ThOBN, Almquist S (1994) Svensk flora: Fanerogamer och ormbunksväxter. Liber, Stockholm

    Google Scholar 

  • Kruskal JB (1964a) Multidimensional scaling by optimizing goodness of fit to a nonmetric hypothesis. Psychometrika 29:1–27

    Article  Google Scholar 

  • Kruskal JB (1964b) Nonmetric multidimensional scaling: a numerical method. Psychometrika 29:28–42

    Google Scholar 

  • Kullman L (1996) Norway spruce present in the Scandes mountains, Sweden at 8000 BP: new light on holocene tree spread. Glob Ecol Biogeogr lett 5:94–101

    Article  Google Scholar 

  • Lagercrantz U, Ryman N (1990) Genetic structure of Norway spruce (Picea abies): concordance of morphological and allozymic variation. Evolution 44:38–53

    Article  Google Scholar 

  • Löve A, Löve D (1974) Origin and the evolution of the arctic and alpine floras. In: Ives JD, Barry RG (eds) Arctic and alpine environments. Methuen, London, pp 571–603

    Google Scholar 

  • Lowe A, Harris S, Ashton P (2004) Ecological genetics—design, analysis and application. Blackwell Publishing, Oxford

    Google Scholar 

  • Lumaret R, Barrientos E (1990) Phylogenetic relationships and gene flow between sympatric diploid and tetraploid plants of Dactylis glomerata (Gramineae). Pl Syst Evol 169:81–96

    Article  Google Scholar 

  • Luttikhuizen PC, Stift M, Kuperus P, van Tienderen PH (2007) Genetic diversity in diploid vs. tetraploid Rorippa amphibia (Brassicaceae). Molec Ecol 16:3544–3553

    Article  CAS  Google Scholar 

  • Malm U, Prentice HC (2002) Immigration history and gene dispersal: allozyme variation in Nordic populations of the red campion, Silene dioica (Caryophyllaceae). Biol J Linn Soc 77:23–34

    Article  Google Scholar 

  • Malm U, Prentice HC (2005) Chloroplast DNA haplotypes in Nordic Silene dioica: postglacial immigration from the east and the south. Pl Syst Evol 250:27–38

    Article  CAS  Google Scholar 

  • Mantel N (1967) The detection of disease clustering and a generalized regression approach. Cancer Res 27:209–220

    PubMed  CAS  Google Scholar 

  • Mossberg B, Nilsson S (1987) Orkidéer- Europas vildväxande arter. Wahlström & Widstrand, Stockholm

    Google Scholar 

  • Mossberg B, Stenberg L (2003) Den nya nordiska floran. Wahlström & Widstrand, Stockholm

    Google Scholar 

  • Nei M, Li WH (1979) Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc Natl Acad Sci USA 76:5269–5273

    Article  PubMed  CAS  Google Scholar 

  • Nordal I, Jonsell B (1998) A phylogeographic analysis of Viola rupestris: three post-glacial immigration routes into the Nordic area? Bot J Linn Soc 128:105–122

    Google Scholar 

  • Nordström S, Hedrén M (2007) Development of polymorphic nuclear microsatellite markers for polyploid and diploid members of the orchid genus Dactylorhiza. Molec Ecol Notes 7:644–647

    Article  Google Scholar 

  • Otto SP, Whitton J (2000) Polyploid incidence and evolution. Ann Rev Genet 34:401–437

    Article  PubMed  CAS  Google Scholar 

  • Palmé AE, Su Q, Rautenberg A, Manni F, Lascoux M (2003) Postglacial recolonization and cpDNA variation of silver birch, Betula pendula. Molec Ecol 12:201–212

    Article  Google Scholar 

  • Pedersen HÆ, Hedrén M, Bateman RM (2003) Proposal to conserve the name Orchis majalis against O. elata, O. vestita and O. sesquipedalis (Dactylorhiza: Orchidinae: Orchidaceae). Taxon 52:633–634

    Article  Google Scholar 

  • Pillon Y, Fay MF, Hedrén M, Bateman RM, Devey DS, Shipunov AB, van der Bank M, Chase MW (2007) Evolution and temporal diversification of western European polyploid species complexes in Dactylohiza (Orchidaceae). Taxon 56:1185–1208

    Google Scholar 

  • Pridgeon AM, Cribb PJ, Chase MW, Rasmussen FN (2001) Genera orchidacearum, 2: 1. Oxford University Press, Oxford

    Google Scholar 

  • Rendell S, Ennos RA (2002) Chloroplast DNA diversity in Calluna vulgaris (heather) populations in Europe. Molec Ecol 11:69–78

    Article  CAS  Google Scholar 

  • Rohlf FJ (2005) NTSYSpc: numerical taxonomy system, ver. 2.20. Exeter Publishing, Ltd., Setauket

    Google Scholar 

  • van Rossum F, Prentice HC (2004) Structure of allozyme variation in Nordic Silene nutans (Caryophyllaceae): population size, geographical position and immigration history. Biol J Linn Soc 81:357–371

    Article  Google Scholar 

  • Senghas K (1968) Taxonomische Übersicht der gattung Dactylorhiza Necker ex Nevski. In: Senghas K, Sundermann H (eds) Probleme der Orchideengattung Dactylorhiza. Jahresber Naturwiss Vereins Wuppertal 21–22:32–67

  • Shipunov AB, Fay MF, Chase MW (2005) Evolution of Dactylorhiza baltica (Orchidaceae) in European Russia: evidence from molecular markers and morphology. Bot J Linn Soc 147:257–274

    Article  Google Scholar 

  • Skrede I, Eidesen PB, Portela RP, Brochmann C (2006) Refugia, differentiation and postglacial migration in arctic-alpine Eurasia, exemplified by the mountain avens (Dryas octopetala L.). Molec Ecol 15:1827–1840

    Article  CAS  Google Scholar 

  • Soliva M, Widmer A (1999) Genetic and floral divergence among sympatric populations of Gymnadenia conopsea s.l. (Orchidaceae) with different flowering phenology. Int J Pl Sci 160:897–905

    Article  Google Scholar 

  • Soltis DE, Rieseberg LH (1986) Autopolyploidy in Tolmiea-menziesii (Saxifragaceae): Genetic insights from enzyme electrophoresis. Amer J Bot 73:310–318

    Article  CAS  Google Scholar 

  • Ståhlberg D (2007) Systematics, phylogeography and polyploid evolution in the Dactylorhiza maculata complex (Orchidaceae). Doctoral dissertation, Lund University, Lund

  • Stewart JR, Lister AM (2001) Cryptic northern refugia and the origins of the modern biota. Trends Ecol Evol 16:608–613

    Article  Google Scholar 

  • Taberlet P, Gielly L, Pautou G, Bouvet J (1991) Universal primers for amplification of three non-coding regions of chloroplast DNA. Pl Molec Biol 17:1105–1109

    Article  CAS  Google Scholar 

  • Taberlet P, Swenson JE, Sandegren F, Bjärvall A (1995) Localization of a contact zone between two higly divergent mitochondrial DNA lineages of the brown bear (Ursus arctos) in Scandinavia. Conserv Biol 9:1255–1261

    Google Scholar 

  • Tyler T, Prentice HC, Widén B (2002) Geographic variation and dispersal history in Fennoscandian populations of two forest herbs. Pl Syst Evol 233:47–64

    Article  Google Scholar 

  • Wolfe AD, Randle CP (2004) Recombination, heteroplasmy, haplotype polymorphism, and paralogy in plastid genes: implications for plant molecular systematics. Syst Bot 29:1011–1020

    Article  Google Scholar 

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Acknowledgments

We would like to thank Sunniva Aagaard, Åse Bøilestad Breivik, Stefan Ericsson, Sven Hansson, Ursula Malm, Lennart Nordström, Tarmo Pikner, Mikko Piirainen, Mari Reitalu, David Ståhlberg, Taavo Tuulik, Kai Vahtra and Finn Wischmann for field assistance and/or collecting material. We also thank two anonymous reviewers for valuable comments. The study was supported by grants from Lunds Botaniska Förening to SN and from the Crafoord Foundation and the Swedish research council for environment, agricultural sciences and spatial planning, FORMAS (grant 2002-102) to MH.

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Correspondence to Sofie Nordström.

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Table 3

Table 3 Identification and geographic origin of populations of Dactylorhiza Neck. ex Nevski used in this study. Latitude and longitude references are approximate

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Nordström, S., Hedrén, M. Genetic differentiation and postglacial migration of the Dactylorhiza majalis ssp. traunsteineri/lapponica complex into Fennoscandia. Plant Syst Evol 276, 73–87 (2008). https://doi.org/10.1007/s00606-008-0084-1

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