2017
DOI: 10.1016/j.ympev.2017.05.026
|View full text |Cite
|
Sign up to set email alerts
|

Correlated evolutionary rates across genomic compartments in Annonaceae

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

4
12
0

Year Published

2018
2018
2019
2019

Publication Types

Select...
8
1

Relationship

4
5

Authors

Journals

citations
Cited by 11 publications
(16 citation statements)
references
References 90 publications
4
12
0
Order By: Relevance
“…These estimates are in the upper range of those inferred from microsatellites (Piñeiro et al., ) but should be more reliable because they essentially depend on a molecular clock calibrated by fossil evidence and do not require a priori assumptions regarding effective population sizes or generation time. However, as our calibration nodes pre‐date the divergence between the subfamilies Annonoideae and Malmeoideae (to which Greenwayodendron belongs) with a substitution rate higher in the Annonoideae (Hoekstra et al., ), the beast analyses may have converged on a posterior distribution of substitution rates that matches that of the Annonoideae, thus resulting in an underestimate of the ages presented here.…”
Section: Discussionmentioning
confidence: 95%
“…These estimates are in the upper range of those inferred from microsatellites (Piñeiro et al., ) but should be more reliable because they essentially depend on a molecular clock calibrated by fossil evidence and do not require a priori assumptions regarding effective population sizes or generation time. However, as our calibration nodes pre‐date the divergence between the subfamilies Annonoideae and Malmeoideae (to which Greenwayodendron belongs) with a substitution rate higher in the Annonoideae (Hoekstra et al., ), the beast analyses may have converged on a posterior distribution of substitution rates that matches that of the Annonoideae, thus resulting in an underestimate of the ages presented here.…”
Section: Discussionmentioning
confidence: 95%
“…This also applies to larger genera in the faster evolving Annonoideae, the challenge of Guatteria (Erkens et al 2007) being a case in point. One alternative currently being explored is to expand plastid datasets using high throughput sequencing (Hoekstra et al 2017; Lopes et al 2018). Whole plastid sequences might be expected to deliver a well-resolved plastid gene tree, but particularly at low taxonomic levels, this might differ markedly from the underlying species tree (Doyle 1992; Maddison 1997).…”
Section: Discussionmentioning
confidence: 99%
“…Different palynological and morphological studies have been conducted in the Annonaceae (Doyle & Le Thomas, , ) which have been highly informative for classifying the different groups in this family (Doyle & Le Thomas, ). More recently, molecular phylogenetic studies mainly using plastid regions ( rbcL, matK, ndhF, trnL, trnT‐L, trnL‐F, trnS‐G, atpB‐rbcL, trnH‐psbA, ycf1, rpl32‐trnL, or ndhF‐rpl32 ) have provided valuable information on specific and general aspects of the Annonaceae (Mols et al, ; Richardson et al, ; Pirie et al, ; Chatrou et al, ; Erkens et al, ; Thomas et al, ; Chaowasku et al, ; Larranaga & Hormaza, ; Tang et al, ; Guo et al, ; Hoekstra et al, ). Annona , described by Linnaeus () and further clarified by Safford (), includes approximately 162 species (Chatrou et al, ), distributed mainly in the Neotropics, with a few species native to Africa.…”
Section: Introductionmentioning
confidence: 99%