2006
DOI: 10.3417/0026-6493(2006)93[49:araeob]2.0.co;2
|View full text |Cite
|
Sign up to set email alerts
|

ADAPTIVE RADIATION AND EVOLUTION OF BREEDING SYSTEMS IN SCHIEDEA (CARYOPHYLLACEAE), AN ENDEMIC HAWAIIAN GENUS1

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
52
0

Year Published

2008
2008
2022
2022

Publication Types

Select...
10

Relationship

2
8

Authors

Journals

citations
Cited by 57 publications
(53 citation statements)
references
References 55 publications
1
52
0
Order By: Relevance
“…For example, observations that the self-fertilizing Mimulus nasutus and serpentine-endemic Mimulus nudatus are found in drier habitats in the Weld suggest that these species are more tolerant of low soil moisture than their presumed progenitor, Mimulus guttatus (Vickery 1978;Kiang and Hamrick 1978;Macnair and Gardner 1998;Hughes et al 2001). Similar distribution patterns have been found with derived selWng species in other taxonomic groups (Gottlieb 2003;Culley et al 2006;Sakai et al 2006). At the other extreme are coastal perennial populations of M. guttatus, that unlike inland annual M. guttatus, occur in habitats where soil moisture is maintained year-round by lower temperatures and persistent fog during summer months (Hall and Willis 2006;Lowry et al 2008).…”
Section: Introductionsupporting
confidence: 66%
“…For example, observations that the self-fertilizing Mimulus nasutus and serpentine-endemic Mimulus nudatus are found in drier habitats in the Weld suggest that these species are more tolerant of low soil moisture than their presumed progenitor, Mimulus guttatus (Vickery 1978;Kiang and Hamrick 1978;Macnair and Gardner 1998;Hughes et al 2001). Similar distribution patterns have been found with derived selWng species in other taxonomic groups (Gottlieb 2003;Culley et al 2006;Sakai et al 2006). At the other extreme are coastal perennial populations of M. guttatus, that unlike inland annual M. guttatus, occur in habitats where soil moisture is maintained year-round by lower temperatures and persistent fog during summer months (Hall and Willis 2006;Lowry et al 2008).…”
Section: Introductionsupporting
confidence: 66%
“…While there have been tremendous advances in our knowledge of the origin and phylogeny of Hawaiian plant and animal radiations (e.g., see Baldwin et al 1991;Givnish et al 1995;Piano et al 1997;Lindqvist et al 2003;Gillespie 2004;Price and Wagner 2004;Rundell et al 2004;Sakai et al 2006), for many of these radiations we lack the functional data necessary to understand the ecological signiWcance of phenotypic divergences seen within them. A body of work has developed on functional trait variation in Hawaiian plant radiations, notably on Euphorbia and Scaevola (Robichaux andPearcy 1980, 1984;Pearcy et al 1982), the silversword alliance (Robichaux 1984;Robichaux and CanWeld 1985;Robichaux et al 1990), and Schiedea (Sakai et al 2006). Our research on the Hawaiian lobeliads adds to this body of literature and contributes to our understanding of the extent of habitat divergence and accompanying functional diversiWcation in the most species-rich Hawaiian Xowering plant lineage.…”
Section: Discussionmentioning
confidence: 99%
“…Among the best studied dioecious taxa, male heterogamety has evolved twice in the genus Silene (Mrackova et al 2008), twice more in the Hawaiian genus Schiedia in the same family, Caryophyllaceae (Sakai et al 2006), and twice yet again in the genus Rumex in another family (Navajas-Perez et al 2005). In all these cases, dioecy probably evolved within the past 10-15 million years (dioecy in Silene is estimated to have evolved more recently than in Rumex, and dioecious Schiedia evolved more recently still).…”
Section: Genetic Mapping Of Sex-determining Regionsmentioning
confidence: 99%