2013
DOI: 10.1016/j.foreco.2013.05.026
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Recent distribution changes affect geographic clines in genetic diversity and structure of Pinus densiflora natural populations in Japan

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Cited by 30 publications
(17 citation statements)
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“…According to Wright [42], the level of genetic differentiation among populations is low when the coefficient of genetic differentiation (F ST ) is less than 0.25. Our results showed that the genetic differentiation level of P. koraiensis was very low (F ST ranging from 0.007 to 0.021), and the AMOVA results showed that only 2.35% of the total genetic variation occurred among populations, which was consistent with conifers often showing low levels of genetic differentiation among populations [35,36,43,44]. Due to their wind pollination and high out-crossing rates, Pinus species, such as P. koraiensis often exhibit high gene flow among populations [45][46][47] and, consequently, a low level of genetic differentiation.…”
Section: Genetic Differentiation and Population Structuresupporting
confidence: 69%
“…According to Wright [42], the level of genetic differentiation among populations is low when the coefficient of genetic differentiation (F ST ) is less than 0.25. Our results showed that the genetic differentiation level of P. koraiensis was very low (F ST ranging from 0.007 to 0.021), and the AMOVA results showed that only 2.35% of the total genetic variation occurred among populations, which was consistent with conifers often showing low levels of genetic differentiation among populations [35,36,43,44]. Due to their wind pollination and high out-crossing rates, Pinus species, such as P. koraiensis often exhibit high gene flow among populations [45][46][47] and, consequently, a low level of genetic differentiation.…”
Section: Genetic Differentiation and Population Structuresupporting
confidence: 69%
“…ellipticus (Aoki et al 2004b), Photinia glabra (Aoki et al 2006), Myrsine seguinii (Aoki et al 2011), and Camellia japonica (Ueno 2015) for plant species, C. hilgendorfi; a specific predator of C. sieboldii seeds (Aoki et al 2008) and Rhynchaenus dorsoplanatus; a specific leaf miner of C. sieboldii leaves (Aoki et al 2010) for insect species. Genetic boundaries between several species of warm to cool temperate zones in Japan also appear to be located in this region, for example, Pinus (Miyata and Ubukata 1994;Iwaizumi et al 2013), Cerasus (Tsuda et al 2009), Zanthoxylum (Yoshida et al 2010), Padus, Carpinus, and Magnolia (Iwasaki et al 2010(Iwasaki et al , 2012, and Acer (Yoshimaru and Matsumoto 2015) for plant species; Curculio (Aoki et al 2009) for insect species; and Cervus (Nagata et al 1999), Macaca (Kawamoto et al 2007), Petaurista (Oshida et al 2009), Ursus (Yasukochi et al 2009), and Lepus (Nunome et al 2010) for mammal species. The common geographic differentiation among multiple codistributed taxa may help efforts to elucidate the relative influence of major historical events such as climate changes during the glacial and interglacial periods (Avise 2000).…”
Section: Discussionmentioning
confidence: 99%
“…The genetic diversity of T . koraiensis was slightly lower than that of conifer species that have widespread geographic ranges, including Thuja occidentalis (mean N A = 8.83; H E = 0.64 in the core populations; mean N A = 6.64; H E = 0.60 in the peripheral populations) [ 68 ], Pinus densiflora (mean N A =14.6; H E = 0.873 within 1883 individuals from 62 natural populations) [ 69 ], and P . orientalis (mean N A = 8.945; H E = 0.832 from 21 populations) [ 70 ].…”
Section: Discussionmentioning
confidence: 99%