2010
DOI: 10.3732/ajb.0900262
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Clonal and spatial genetic structure within populations of a coastal plant, Carex kobomugi (Cyperaceae)

Abstract: Clarification of clonal growth pattern is critical for understanding the population dynamics and reproductive system evolution of clonal plant species. The contribution of clonality to the spatial genetic structure (SGS) within populations is also an important issue. I examined the spatial distribution of genetic variability within two populations of the coastal plant Carex kobomugi using seven microsatellite loci. Genotyping of 226 and 140 ramets within 14 × 40 m and 14 × 34 m plots on two populations reveale… Show more

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Cited by 38 publications
(35 citation statements)
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References 52 publications
(74 reference statements)
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“…A meta-analysis of 77 clonal plant species produced mean Simpson's D ¼ 0Á85 and Fager's E ¼ 0Á74 (Honnay and Jacquemyn, 2008), which was similar to the six kudzu patches except HDP (Table 1). Yet the range of mean clonal dominance among kudzu patches (0Á35-0Á93) exceeded the interspecific range (0Á42-0Á89) among eight comparable studies (Ohsako, 2010). These kudzu patches also had more variable b values than 15 terrestrial and marine plant species (kudzu ¼ 0Á03-1Á47; other species ¼ 0Á60-1Á49; Ohsako, 2010) as well as four sea grass populations with the broadest intraspecific range previously reported (Posidonia oceanica ¼ 0Á06-1Á23; Arnaud-Haond et al, 2007).…”
Section: Discussionmentioning
confidence: 94%
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“…A meta-analysis of 77 clonal plant species produced mean Simpson's D ¼ 0Á85 and Fager's E ¼ 0Á74 (Honnay and Jacquemyn, 2008), which was similar to the six kudzu patches except HDP (Table 1). Yet the range of mean clonal dominance among kudzu patches (0Á35-0Á93) exceeded the interspecific range (0Á42-0Á89) among eight comparable studies (Ohsako, 2010). These kudzu patches also had more variable b values than 15 terrestrial and marine plant species (kudzu ¼ 0Á03-1Á47; other species ¼ 0Á60-1Á49; Ohsako, 2010) as well as four sea grass populations with the broadest intraspecific range previously reported (Posidonia oceanica ¼ 0Á06-1Á23; Arnaud-Haond et al, 2007).…”
Section: Discussionmentioning
confidence: 94%
“…We further characterized the spatial distribution of genets by calculating the index of clonal dominance, D c ¼ (N S -1)/ (N T -1), where N S is the number of ramets belonging to a focal genet and N T is the total number of ramets sampled within the range of the focal genet (Ohsako, 2010). This value was calculated for genets represented by !3 ramets in a patch, where a convex hull could circumscribe each genet.…”
Section: Clonal Analysismentioning
confidence: 99%
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“…1 Map of the study site Wielka Kępa natural reserve along Vistula river in Poland the number of sampled individuals (ramets) (Dorken and Eckert 2001). Clonal architecture was expressed with a clonal dominance index (Dc) calculated following Ohsako (2010) for each of the sexes for each clone with ≥3 ramets:…”
Section: Clonality and Clonal Architecturementioning
confidence: 99%
“…Short rhizomes result in aggregated clusters of ramets within genets (that is, phalanx growth strategy) while longer rhizomes can spread in multiple directions over longer distances (that is, guerrilla growth strategy) such that different genets may intersect (Lovett Doust, 1981). Aggregated phalanx growth not only results in stronger patterns of fine-scale genetic structure but also increases the chances of geitonogamous selfing, particularly with increasing genet size, and consequently increases the risk of inbreeding depression (Charpentier, 2002;Albert et al, 2008;Ohsako, 2010).…”
Section: Introductionmentioning
confidence: 99%