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The Expansion Route of Ryegrasses (Lolium spp.) into Sandy Coasts in Japan

Published online by Cambridge University Press:  27 April 2017

Yumiko Higuchi ,
Yoshiko Shimono  and
Tohru Tominaga
Yumiko Higuchi*
Affiliation:
Graduate Student, Center for Ecological Research, Kyoto University, 509-3, 2-chome, Hirano, Otsu, Shiga, Japan, 520-2113
Yoshiko Shimono
Affiliation:
Assistant Professor and Professor, Laboratory of Weed Science, Graduate School of Agriculture, Kyoto University, Oiwake-cho, Kitashirakawa, Sakyo-ku, Kyoto, Kyoto, Japan, 606-8502
Tohru Tominaga*
Affiliation:
Assistant Professor and Professor, Laboratory of Weed Science, Graduate School of Agriculture, Kyoto University, Oiwake-cho, Kitashirakawa, Sakyo-ku, Kyoto, Kyoto, Japan, 606-8502
*
*Corresponding author’s E-mail: ymhiguchi@ecology.kyoto-u.ac.jp
*Corresponding author’s E-mail: ymhiguchi@ecology.kyoto-u.ac.jp
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Abstract

Although an increasing number of investigations have been made into the evolution of alien species once introduced, few studies have identified the invasion routes of these introduced species. Because multiple introductions are common in invasive species, failing to take into account the introduced lineages can be misleading when studying evolutionary change in alien species after they begin to extend their ranges. In Japan, diverse lineages of ryegrasses (Lolium spp.) were introduced as forage crops and contaminants in trading grain and have expanded to sandy coasts. We studied the expansion route of populations established along the coasts of three geographic regions within Japan by comparing variations in morphology and nuclear microsatellite and chloroplast DNA in the two habitats where ryegrasses were first introduced: croplands and international seaports. Chloroplast DNA haplotypes did not differ significantly among habitats and regions, but the coastal and seaport populations displayed similar microsatellite genetic compositions and morphological characteristics. Our results revealed that coastal populations originated from seaport populations derived from contaminants. Selective forces from the past, including domestication and naturalization, may have assisted the introduced lineages in colonizing new habitats.

Keywords

Italian ryegrass, Lolium multiflorum L.rigid ryegrass, Lolium rigidum GaudinExoticgenetic diversityintentional/unintentional introductionintroduction pathwaysnSSRpostintroduction process
Type
Research and Education
Information
Invasive Plant Science and Management , Volume 10 , Issue 1 , March 2017 , pp. 61 - 71
Copyright
© Weed Science Society of America, 2017 

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Footnotes

Associate Editor for this paper: Jacob N. Barney, Virginia Tech.

References

Literature Cited

Akaike, H (1973) Information theory and an extension of the maximum likelihood principle. Pages 199–213 in Selected Papers of Hirotugu Akaike Parzen E, Tanabe K & Kitagawa G, eds. Springer Series in Statistics New York: Springer Google Scholar
Asai, M, Kurokawa, S, Shimizu, N, Enomoto, T (2007) Exotic weed seeds detected from imported small cereal grains into Japan during 1990s’. J Weed Sci Tec 52:1–10 Google Scholar
Asai, M, Yogo, Y (2005) Occurrence and background of wild oats and Italian ryegrass in winter cereals in the Kanto-Tokai region. J Weed Sci Tec 50:73–81 Google Scholar
Balfourier, F, Imbert, C, Charmet, G (2000) Evidence for phylogeographic structure in Lolium species related to the spread of agriculture in Europe. A cpDNA study. Theor Appl Genet 101:131–138 Google Scholar
Barbour, MG (1978) Salt spray as a microenvironmental factor in the distribution of beach plants at Point Reyes, California. Oecologia 32:2213–2224 Google Scholar
Bennett, SJ (1997) A phenotypic analysis and lateral key of the genus Lolium (Gramineae). Genet Res Crop Evol 44:63–72 Google Scholar
Bennett, SJ, Hayward, MD, Marshall, DF (2000) Morphological differentiation in four species of the genus Lolium . Genet Res Crop Evol 47:247–255 Google Scholar
Blackburn, TM, Pyšek, P, Bacher, S, Carlton, JT, Duncan, RP, Jarošík, V, Wilson, JRU, Richardson, DM (2011) A proposed unified framework for biological invasions. Trends Ecol Evol 26:333–339 Google Scholar
Blacket, MJ, Robin, C, Good, RT, Lee, SF, Miller, AD (2012) Universal primers for fluorescent labelling of PCR fragments—an efficient and cost-effective approach to genotyping by fluorescence. Mol Ecol Resour 12:456–463 Google Scholar
Bossdorf, O, Auge, H, Lafuma, L, Rogers, WE, Siemann, E, Prati, D (2005) Phenotypic and genetic differentiation between native and introduced plant populations. Oecologia 144:1–11 Google Scholar
Chauhan, BS, Gill, G, Preston, C (2006) Influence of environmental factors on seed germination and seedling emergence of rigid ryegrass (Lolium rigidum). Weed Sci 54:1004–1012 CrossRefGoogle Scholar
Chun, YJ, Femanal, B, Laitung, B, Bretagnolle, F (2009) Gene flow and population admixture as the primary post-invasion processes in common ragweed (Ambrosia artemisiifolia) populations in France. New Phytol 185:1100–1107 Google Scholar
Colautti, RI, Barrett, SCH (2013) Rapid adaptation to climate facilitates range expansion of an invasive plant. Science 342:364–366 Google Scholar
Colautti, RI, Lau, JA (2015) Contemporary evolution during invasion: evidence for differentiation, natural selection, and local adaptation. Mol Ecol 24:1999–2017 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. Mol Ecol 4:129–134 Google Scholar
Dietz, H, Edwards, PJ (2006) Recognition that causal process change during plant invasion helps explain conflicts in evidence. Ecology 87:1359–1367 CrossRefGoogle ScholarPubMed
Dlugosch, KM, Parker, IM (2008) Founding events in species invasions: genetic variation, adaptive evolution, and the role of multiple introductions. Mol Ecol 17:431–449 Google Scholar
Dormontt, EE, Lowe, AJ, Prentis, PJ (2011) Is rapid adaptive evolution important in successful invasion? Pages 175–194 in Richardson DM ed. Fifty Years of Invasion Ecology: The Legacy of Charles Elton. London: Blackwell Google Scholar
Estoup, A, Guillemaud, T (2010) Reconstructing routes of invasion using genetic data: why, how and so what? Mol Ecol 19:4113–4130 Google Scholar
Evanno, G, Regnaut, S, Goudet, J (2005) Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol Ecol 14:2611–2620 Google Scholar
Geng, YP, Pan, XY, Xu, CY, Zhang, WJ, Li, B, Chen, JK, Lu, BR, Song, ZP (2007) Phenotypic plasticity rather than locally adapted ecotypes allows the invasive alligator weed to colonize a wide range of habitats. Biol Invasions 9:245–256 Google Scholar
Genton, BJ, Shykoff, JA, Giraud, T (2005) High genetic diversity in French invasive populations of common ragweed, Ambrosia artemisiifolia, as a result of multiple sources of introduction. Mol Ecol 14:4275–4285 CrossRefGoogle ScholarPubMed
Goudet, J (2001) FSTAT, A Program to Estimate and Test Gene Diversities and Fixation Indices, v. 2.9.3. http://www.unil.ch/izea/softwares/fstat.html. Accessed: August 2, 2016Google Scholar
Hao, JH, Qiang, S, Chrobock, T, van Kleunen, M, Liu, QQ (2011) A test of Baker’s law: breeding systems of invasive species of Asteraceae in China. Biol Invasions 13:571–580 Google Scholar
Hirata, M, Cai, H, Inoue, M, Yuyama, N, Miura, Y, Komatsu, T, Takamizo, T, Fujimori, M (2006) Development of simple sequence repeat (SSR) markers and construction of an SSR-based linkage map in Italian ryegrass (Lolium multiflorum Lam.). Theor Appl Genet 113:270–279 CrossRefGoogle ScholarPubMed
Hulme, PE, Bacher, S, Kenis, M, Klotz, S, Kühn, I, Minchin, D, Nentwig, W, Olenin, S, Panov, V, Pergl, J, Pyšek, P, Roques, A, Sol, D, Solarz, W, Vilà, M (2008) Grasping at the routes of biological invasions: a framework for integrating pathways into policy. J Appl Ecol 45:403–414 Google Scholar
Humphreys, M, Feuerstein, U, Vandewalle, M, Baert, J (2010) Ryegrasses. Pages 211–260 in Boller B, Posselt UK & Veronesi F eds. Fodder Crops and Amenity Grasses. Handbook of Plant Breeding. New York: Springer Google Scholar
Kawecki, TJ, Ebert, D (2004) Conceptual issues in local adaptation. Ecol Lett 7:1225–1241 Google Scholar
Keller, SR, Taylor, DR (2008) History, chance and adaptation during biological invasion: separating stochastic phenotypic evolution from response to selection. Ecol Lett 11:852–866 Google Scholar
Keller, SR, Taylor, DR (2010) Genomic admixture increases fitness during a biological invasion. J Evol Biol 23:1720–1731 Google Scholar
Kolbe, JJ, Glor, RE, Schettino, LR, Lara, AC, Larson, A, Losos, JB (2004) Genetic variation increases during biological invasion by a Cuban lizard. Nature 431:177–181 Google Scholar
Kurokawa, S, Kobayashi, H, Ikeda, K (2010) Genetic background of an invasive Lolium population in central Japan using chloroplast DNA and SSR markers. Weed Res 50:245–252 Google Scholar
Lambrinos, JG (2004) How interactions between ecology and evolution influence contemporary invasion dynamics. Ecology 85:2061–2070 Google Scholar
Lavergne, S, Molofsky, J (2007) Increased genetic variation and evolutionary potential drive the success of an invasive grass. Proc Natl Acad Sci USA 104:3883–3888 Google Scholar
Leger, EA, Espeland, EK, Merrill, KR, Meyer, SE (2009) Genetic variation and local adaptation at a cheatgrass (Bromus tectorum) invasion edge in western Nevada. Mol Ecol 18:4366–4379 Google Scholar
Leimu, R, Fischer, MA (2008) Meta-analysis of local adaptation in plants. PLoS One 3:e4010 Google Scholar
Le Roux, JJ, Wieczorek, AM, Meyer, JY (2008) Genetic diversity and structure of the invasive tree Miconia calvescens in Pacific islands. Divers Distrib 14:935–948 Google Scholar
Li, X, She, D, Zhang, D, Liao, W (2015) Life history trait differentiation and local adaptation in invasive populations of Ambrosia artemisiifolia in China. Oecologia 177:669–677 CrossRefGoogle ScholarPubMed
Lockwood, JL, Hoopes, MF, Marchetti, MP (2013) Invasion Ecology 2nd Edn. Hoboken, NJ: Wiley-Blackwell. Pp 277–298 Google Scholar
Lowry, DB, Rockwood, RC, Willis, JH (2008) Ecological reproductive isolation of coast and inland races of Mimulus guttatus . Evolution 62:2196–2214 Google Scholar
Maron, JL, Vilà, M, Bommarro, R, Elmendorf, S, Beardsley, P (2004) Rapid evolution of an invasive plant. Ecol Monogr 74:261–280 Google Scholar
Marshall, TC, Slate, J, Kruuk, LEB, Pemberton, JM (1998) Statistical confidence for likelihood-based paternity inference in natural populations. Mol Ecol 7:639–655 Google Scholar
Maun, MA (1994) Adaptations enhancing survival and establishment of seedlings on coastal dune systems. Vegetatio 111:59–70 CrossRefGoogle Scholar
Ministry of Finance, Japan (2014) Trade Statistics of Japan. http://www.customs.go.jp/toukei/info/index_e.html. Accessed: January 11, 2016Google Scholar
Ministry of Land, Infrastructure, Transport and Tourism (2013) Kouwan-Toukei. http://www.mlit.go.jp/k-toukei/syousaikensaku.html. Accessed January 11, 2016Google Scholar
Murray, MG, Thompson, WF (1980) Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res 8:4321–4326 Google Scholar
Murrumbidgee Catchment Management Authorities, NSW, Australia (2008) Annual ryegrass. Best Management Practices for Dryland Cropping Systems. http://archive.lls.nsw.gov.au. Accessed: January 11, 2016Google Scholar
National Institute for Environmental Studies (2015) Invasive Species of Japan. https://www.nies.go.jp/biodiversity/invasive/index_en.html. Accessed: October 28, 2016Google Scholar
Naylor, B (1960) Species differentiation in the genus Lolium . Heredity 15:219–233 CrossRefGoogle Scholar
Owen, MJ, Martinez, NJ, Powles, SB (2014) Multiple herbicide-resistant Lolium rigidum (annual ryegrass) now dominates across the Western Australian grain belt. Weed Res 54:314–324 CrossRefGoogle Scholar
Peakall, R, Smouse, PE (2012) GenAlEx 6.5: Genetic analysis in Excel. Population genetic software for teaching and research—an update. Bioinformatics 28:2537–2539 Google Scholar
Peter-Schmid, MKI, Boller, B, Kölliker, R (2008) Habitat and management affect genetic structure of Festuca pratensis but not Lolium multiflorum ecotype populations. Plant Breed 127:510–517 Google Scholar
Pritchard, JK, Stephens, M, Donnelly, P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959 Google Scholar
R Development Core Team (2013) R: A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing Google Scholar
Rengasamy, P (2006) World salinization with emphasis on Australia. J Exp Bot 57:1017–1023 Google Scholar
Ridley, CE, Ellstrand, NC (2010) Rapid evolution of morphology and adaptive life history in the invasive California wild radish (Raphanus sativus) and the implications for management. Evol Appl 3:64–76 Google Scholar
Ridley, CE, Kim, SC, Ellstrand, NC (2008) Bidirectional history of hybridization in California wild radish, Raphanus sativus (Brassicaceae), as revealed by chloroplast DNA. Am J Bot 95:1437–1442 Google Scholar
Sakai, AK, Allendorf, FW, Holt, JS, Lodge, DM, Molofsky, J, With, KA, Baughman, S, Cabin, RJ, Cohen, JE, Ellstrand, NCE, McCauley, DE, O’Neil, P, Parker, IM, Thompson, JN, Weller, SJ (2001) The population biology of invasive species. Annu Rev Ecol Evol Syst 32:305–332 Google Scholar
Sampoux, J, Baudouin, P, Bayle, B, Béguier, V, Bourdon, P, Chosson, J, Deneufbourg, F, Galbrun, C, Ghesquière, M, Noël, D, Pietraszek, W, Tharel, B, Viguié, A (2011) Breeding perennial grasses for forage usage: an experimental assessment of trait changes in diploid perennial ryegrass (Lolium perenne L.) cultivars released in the last four decades. Field Crops Res 123:117–129 CrossRefGoogle Scholar
Sax, DF, Stachowicz, JJ, Brown, JH, Bruno, JF, Dawson, MN, Gaines, SD, Grosberg, RK, Hastings, A, Holt, RD, Mayfield, MM, O’Connor, MI, Rice, WR (2007) Ecological and evolutionary insights from species invasions. Trends Ecol Evol 22:465–471 Google Scholar
Shimizu, T (2003) Naturalized Plants in Japan. Tokyo: Heibonsha. Pp 246–247 Google Scholar
Shimono, Y, Takiguchi, Y, Konuma, A (2010) Contamination of internationally traded wheat by herbicide-resistant Lolium rigidum . Weed Biol Manag 10:219–228 Google Scholar
Shimono, Y, Shimono, A, Oguma, H, Konuma, A, Tominaga, T (2015) Establishment of Lolium species resistant to acetolactate synthase-inhibiting herbicide in and around grain-importation ports in Japan. Weed Res 55:101–111 Google Scholar
Shirk, RY, Hamrick, JL, Zhang, C, Qiang, S (2014) Patterns of genetic diversity reveal multiple introductions and recurrent founder effects during range expansion in invasive populations of Geranium carolinianum (Geraniaceae). Heredity 112:497–507 Google Scholar
Suarez, AV, Tsutsui, ND (2008) The evolutionary consequences of biological invasions. Mol Ecol 17:351–360 Google Scholar
Sunnucks, P (2000) Efficient genetic markers for population biology. Trends Ecol Evol 15:199–203 Google Scholar
Terrell, EE (1966) Taxonomic implications of genetics in ryegrasses (Lolium). Bot Rev 32:138–164 Google Scholar
Terrell, EE (1968) A Taxonomic Revision of the Genus Lolium. Technical Bulletin 1392. Washington, DC: Agricultural Research Service, U.S. Department of Agriculture. 65 pGoogle Scholar
Weir, BS, Cockerham, CC (1984) Estimating F-statistics for the analysis of population structure. Evolution 38:1358–1370 Google ScholarPubMed
Wolfe, KH, Li, WH, Sharp, PM (1987) Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs. Proc Natl Acad Sci USA 84:9054–9058 Google Scholar
Yamada, T, Forster, JW, Humphreys, MW, Takamizo, T (2005) Genetics and molecular breeding in Lolium/Festuca grass species complex. Grassl Sci 51:89–106 Google Scholar
Yasuda, K, Shibayama, H (2006) Primer sets for DNA amplification of the noncoding regions of the chloroplast genome in the grass family. J Weed Sci Tec 51:146–151 Google Scholar
Yokoyama, H (2005) The postwar wheat policy and the supply, demand and production of wheat. Agric Econom Soc Jpn 77:113–128 Google Scholar
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