2016
DOI: 10.3732/ajb.1600105
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Ecological distributions, phenological isolation, and genetic structure in sympatric and parapatric populations of theLarrea tridentatapolyploid complex

Abstract: Diploid, tetraploid, and hexaploid cytotypes of L. tridentata are segregated by environmental distributions and flowering phenology in contact zones, with diploid and tetraploid populations having corresponding differences in genetic structure.

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Cited by 47 publications
(61 citation statements)
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References 127 publications
(206 reference statements)
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“…Furthermore, in Galax urceolata complex, tetraploids have experienced niche contraction and divergence with respect to the ancestral wide niche of diploids (Gaynor et al ., ). Contrariwise, in cases where low ploidy cytotypes were unable to expand to occupy their full potential niche (Lowry & Lester, ), and/or multiple polyploid origins occur, the higher levels could experience niche expansion, as in Aster amellus (Münzbergová et al ., ), Claytonia perfoliata (McIntyre, ), Larrea tridentata (Laport et al ., ) or Senecio carniolicus (Sonnleitner et al ., ). These are dynamic systems with frequent coexistence in mixed‐ploidy populations (Kolář et al ., ), and where the apparent competitive superiority of the higher cytotypes may be enhanced by their recurrent polyploid formation and the alleged unfilled niches of lower ploidies.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, in Galax urceolata complex, tetraploids have experienced niche contraction and divergence with respect to the ancestral wide niche of diploids (Gaynor et al ., ). Contrariwise, in cases where low ploidy cytotypes were unable to expand to occupy their full potential niche (Lowry & Lester, ), and/or multiple polyploid origins occur, the higher levels could experience niche expansion, as in Aster amellus (Münzbergová et al ., ), Claytonia perfoliata (McIntyre, ), Larrea tridentata (Laport et al ., ) or Senecio carniolicus (Sonnleitner et al ., ). These are dynamic systems with frequent coexistence in mixed‐ploidy populations (Kolář et al ., ), and where the apparent competitive superiority of the higher cytotypes may be enhanced by their recurrent polyploid formation and the alleged unfilled niches of lower ploidies.…”
Section: Discussionmentioning
confidence: 99%
“…This process can enhance the genetic diversity of a nascent polyploid population and potentially mitigate the consequences of inbreeding among a small number of autopolyploids (Bretagnolle & Thompson, 1995). The evolutionary importance of gene flow between diploids and tetraploids was noted by Stebbins (1971), and the contributions of intercytotype gene flow on genetic diversity have since been reported in autopolyploid Dactylorhiza maculata (Ståhlberg, 2009), Houstonia (Glennon & Church, 2015), and Larrea tridentata (Laport et al, 2016). Selection on new autopolyploids may therefore be complex, with potentially opposing pressures-complete reproductive isolation from diploid progenitors (through prezygotic or postzygotic mechanisms) will counteract the deleterious effects of MCE by preventing often-unsuccessful intercytotype mating, but maintaining reproductive overlap with diploids may provide the benefit of increased genetic diversity through rare introgression via unreduced gametes.…”
Section: Gene Flow Between Cytotypesmentioning
confidence: 95%
“…Empirical support for this prediction is mixed (Vellend 2016), but more importantly this prediction does not consider that different mechanisms of speciation can cause differences in SPFD among regions. For example, sympatric speciation can occur via polyploidy in plants (Levin 1975, Husband andSchemske 2000) and this can result in polyploids occupying distinct niches from their diploid progenitors (e.g., Laport et al 2016, Ostevik et al 2016. In such a case, speciation in one region may concurrently increase species pool richness and SPFD ( Fig.…”
Section: Speciationmentioning
confidence: 99%