2017
DOI: 10.1086/691460
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Polyploidization and Genome Size Evolution in Australian Billy Buttons (Craspedia, Asteraceae: Gnaphalieae)

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Cited by 8 publications
(7 citation statements)
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“…Genome size is an important characteristic for a species that is related in part to the ploidy level, plant physiology, ecology and genome evolution (Heslop-Harrison 1995). Genome size studies of polyploids have contributed to improving the knowledge of the process of polyploid formation (Bures et al 2004;Poggio et al 2014;Castelli et al 2017). Many studies of other turfgrasses using laser flow cytometry have demonstrated that nuclear DNA content is closely correlated with chromosome number, and thus ploidy level (Johnson et al 1998;Eaton et al 2004).…”
Section: Introductionmentioning
confidence: 99%
“…Genome size is an important characteristic for a species that is related in part to the ploidy level, plant physiology, ecology and genome evolution (Heslop-Harrison 1995). Genome size studies of polyploids have contributed to improving the knowledge of the process of polyploid formation (Bures et al 2004;Poggio et al 2014;Castelli et al 2017). Many studies of other turfgrasses using laser flow cytometry have demonstrated that nuclear DNA content is closely correlated with chromosome number, and thus ploidy level (Johnson et al 1998;Eaton et al 2004).…”
Section: Introductionmentioning
confidence: 99%
“…The hypothesis of a paleopolyploid origin of the Australasian clade (Smissen & al., 2011) and the observation that some genera represent polyploid complexes (Kokubugata & Holland, 2002;Castelli & al., 2017) suggest that paralogy should be expected, and our data showed paralogy in 176 genes. We resolved the issue by excluding the affected genes after preliminary analyses indicated that phylogenies produced using the other ortholog resolution approaches implemented by Yang & Smith (2014), which would have increased the number of available genes, did not provide notably better resolution and branch support (not shown).…”
Section: ■ Resultsmentioning
confidence: 99%
“…Fresh leaf material was collected from living specimens and kept on ice. A single triploid clone of Bellis perennis L. (2C = 3.41 pg DNA) was used as a standard (Castelli, Miller, & Schmidt‐Lebuhn, ). Approximately 50 mg of Rutidosis lanata and 10 mg of standard leaf material were each placed in 1,200 μl of ice‐cold Modified Galbraith's buffer (Galbraith et al., ; Price, ) [4.58 g MgCl2, 2.1 g MOPSO, 4.44 g Citric Acid, 15.0 g PVP‐10, 0.5 ml Triton X‐100, 2.5 ml Tween 20, made up to 500 ml with distilled water.…”
Section: Methodsmentioning
confidence: 99%