2018
DOI: 10.1016/j.aquabot.2018.05.002
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Genetic structure of Hydrilla verticillata L.f. Royle in eastern China and the Republic of Korea: Implications for surveys of biological control agents for the invasive monoecious biotype

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Cited by 13 publications
(12 citation statements)
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“…Monoecious plants were discovered in Delaware in 1976 and spread subsequently to every state from North Carolina to Maine (Les et al, 1997;Madeira et al, 2000), as well as to California, Georgia, Indiana, Washington, and Wisconsin (Keller, 2007;Jacono et al, 2019b). Although both U.S. biotypes for the most part are triploid (Harlan et al, 1984;Langeland, 1989;Les et al, 1997), other genetic, morphological, and physiological differences have been documented between monoecious and dioecious plants, including distinct plastid sequences (Madeira et al, 2004(Madeira et al, , 2007Williams et al, 2018), microsatellite signatures (Williams et al, 2018), vegetative morphologies (Ryan et al, 1995), isozyme profiles (Verkleij and Pieterse, 1991;Nakamura et al, 1998), and tuber production patterns (Scannell and Webb, 1976;Steward and Van, 1987;Sutton et al, 1992;Nakamura and Kadono, 1993).…”
Section: Author Manuscriptmentioning
confidence: 99%
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“…Monoecious plants were discovered in Delaware in 1976 and spread subsequently to every state from North Carolina to Maine (Les et al, 1997;Madeira et al, 2000), as well as to California, Georgia, Indiana, Washington, and Wisconsin (Keller, 2007;Jacono et al, 2019b). Although both U.S. biotypes for the most part are triploid (Harlan et al, 1984;Langeland, 1989;Les et al, 1997), other genetic, morphological, and physiological differences have been documented between monoecious and dioecious plants, including distinct plastid sequences (Madeira et al, 2004(Madeira et al, , 2007Williams et al, 2018), microsatellite signatures (Williams et al, 2018), vegetative morphologies (Ryan et al, 1995), isozyme profiles (Verkleij and Pieterse, 1991;Nakamura et al, 1998), and tuber production patterns (Scannell and Webb, 1976;Steward and Van, 1987;Sutton et al, 1992;Nakamura and Kadono, 1993).…”
Section: Author Manuscriptmentioning
confidence: 99%
“…Intraspecific hybridization could be possible among hydrilla lineages that are genetically distinct, with some plastid clades having diverged ~6.71 mya (Zhu et al, 2015). Besides being genetically distinct, many plastid lineages are relatively isolated across the wide geographic range of the genus, allowing them to evolve independently (Stebbins, 1950;Cook and Lüönd, 1982;Williams et al, 2018). Hybridization, whether interspecific between nonindigenous and native species or intraspecific between individuals from different donor ranges, may produce novel genotypes that enhance adaptation to new environments (Ellstrand and Schierenbeck, 2000;Moody and Les, 2002;Bossdorf et al, 2005), and this possibility becomes a serious consideration in the context of invasive hydrilla populations.…”
Section: Author Manuscriptmentioning
confidence: 99%
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“…First, the geographic source of introduced populations must be located (Goolsby et al 2006). This is commonly done through molecular matching techniques in which plant tissues from introduced populations are sampled, their DNA is extracted and analyzed, then compared with samples from native populations (Williams et al 2018). This approach is especially important when the species have large geographic ranges because control agents may be locally adapted to a particular plant genotype (Boughton andPemberton 2011, Mukwevho et al 2017).…”
Section: Available Means Of Controlmentioning
confidence: 99%