Molecular phylogenetic and biogeographical analysis of Nitraria based on nuclear and chloroplast DNA sequences

Temirbayeva, K.; Zhang, Mingli

doi:10.1007/s00606-015-1202-5

Cited by 26 publications

(34 citation statements)

References 38 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…In the last decade, researchers have made important contributions to our understanding of the evolution and diversification within the Sapindales. The order has been suggested to be monophyletic (e.g., Muellner & al., 2007), evolutionary relationships within and among families have been identified (albeit many uncertainties remained; e.g., Muellner & al., 2003Muellner & al., , 2006Muellner & al., , 2007Clayton & al., 2009;Groppo & al., 2012;Buerki & al., 2010Buerki & al., , 2013Morton & Telmer, 2014;Weeks & al., 2014;Koenen & al., 2015;Temirbayeva & Zhang, 2015), morphological, anatomical, and structural links between families have been uncovered (e.g., Bachelier & Endress, 2008), and domestication histories have been elucidated (e.g., Miller & Schaal, 2006).…”

Section: Introductionmentioning

confidence: 99%

“…(2007) tested the monophyly and placement of monogeneric Biebersteiniaceae, supporting Biebersteiniaceae as monophyletic, possibly sister to the other eight families of Sapindales. The latest phylogenetic study comprising Nitrariaceae taxa was done by Temirbayeva & Zhang (2015), but it included only two out of four genera, Nitraria L. and Peganum L. Previously, Muellner & al. (2007) had included all four genera (albeit represented by only a single species each), supporting Nitrariaceae as monophyletic, in an unsupported grade that included Biebersteiniaceae.…”

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

Molecular phylogenetics and molecular clock dating of Sapindales based on plastid rbcL, atpB and trnL-trnF DNA sequences

Muellner‐Riehl

Weeks

Clayton

et al. 2016

TAXON

113

View full text Add to dashboard Cite

This study focuses on reconstructing the time‐calibrated phylogeny of the nine families comprising the order Sapindales, representing a diverse and economically important group of eudicots including citrus, mahogany, tree‐of‐heaven, cashew, mango, pistachio, frankincense, myrrh, lychee, rambutan, maple, and buckeye. We sampled three molecular markers, plastid genes rbcL and atpB, and the trnL‐trnLF spacer region, and covered one‐third of the generic diversity of Sapindales. All three markers produced congruent phylogenies using maximum likelihood and Bayesian methods for a set of taxa that included outgroups, i.e., members of the closely related orders Brassicales and Malvales, and the more distantly related Crossosomatales, Ranunculales, and Ceratophyllales. All results confirmed the current delimitation of the families within Sapindales, and the monophyly of the order. Concerning inter‐familial relationships, Biebersteiniaceae and Nitrariaceae formed a basal grade (or sister clade) to the rest of Sapindales with moderate support. The sister relationship of Kirkiaceae to Anacardiaceae and Burseraceae was strongly supported. The clade combining Anacardiaceae and Burseraceae as well as the clade combining Meliaceae, Simaroubaceae, and Rutaceae each received strong support. The sister relationship between Meliaceae and Simaroubaceae was moderately supported. The position of Sapindaceae could not be resolved with confidence. The Sapindales separated from their sister clade, comprising Brassicales and Malvales, in the Early Cretaceous at ca. 112 Ma, and diversified into the nine families from ca. 105 Ma until ca. 87 Ma during Early to Late Cretaceous times. Biebersteiniaceae and Nitrariaceae have the longest stem lineages observed in Sapindales, possibly indicating that extinction may have had a greater role in shaping their extant diversity than elsewhere within the order. Divergence within the larger families (Anacardiaceae, Burseraceae, Meliaceae, Rutaceae, Sapindaceae, Simaroubaceae) started during the Late Cretaceous, extending into the Paleogene and Neogene.

show abstract

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Molecular phylogenetics and molecular clock dating of Sapindales based on plastid rbcL, atpB and trnL-trnF DNA sequences

Muellner‐Riehl

Weeks

Clayton

et al. 2016

TAXON

113

View full text Add to dashboard Cite

show abstract

“…Seven DNA fragments, i.e., nr DNA ITS and cp DNA rbc L, trn G-S, atp B- rbc L, psb A- trn H, psb B-H, and mat K, were sequenced as described previously230. An aligned data set of 7601 nucleotide positions was used for phylogenetic dating.…”

Section: Methodsmentioning

confidence: 99%

Himalayan uplift shaped biomes in Miocene temperate Asia: evidence from leguminous Caragana

Zhang

Xiang

Xue

et al. 2016

Sci Rep

Self Cite

View full text Add to dashboard Cite

Caragana, with distinctive variation in leaf and rachis characters, exhibits three centers of geographic distribution, i.e., Central Asia, the Qinghai-Tibetan Plateau (QTP), and East Asia, corresponding to distinct biomes. Because Caragana species are often ecologically dominant components of the vegetation in these regions, it is regarded as a key taxon for the study of floristic evolution in the dry regions of temperate Asia. Based on an expanded data set of taxa and gene regions from those previously generated, we employed molecular clock and biogeographical analyses to infer the evolutionary history of Caragana and link it to floristic patterns, paleovegetation, and paleoclimate. Results indicate that Caragana is of arid origin from the Junggar steppe. Diversification of crown group Caragana, dated to the early Miocene ca. 18 Ma and onwards, can be linked to the Himalayan Motion stage of QTP uplift. Diversification of the major clades in the genus corresponding to taxonomic sections and morphological variation is inferred to have been driven by the uplift, as well as Asian interior aridification and East Asian monsoon formation, in the middle to late Miocene ca. 12~6 Ma. These findings demonstrate a synchronous evolution among floristics, vegetation and climate change in arid Central Asia, cold arid alpine QTP, and mesophytic East Asia.

show abstract

“…植物区系的始生性质 (Wulff, 1964) Komarov, 1945;Wulff, 1964; 路安民 , Komarov (1908Komarov ( , 1947 (Nylander et al, 2008;Ree & Smith, 2008;Yu et al, 2015), 为区系地理研究提供了有效的方法, 在一定程度上能够给出科属类群较确切的起源时间和起源地点。虽然这些方法应用于干旱区植物类群的研究并不多, 但也有一些典型的案例, 例如对蒿属(Artemisia) (Miao et al, 2011)、锦鸡儿属 (Zhang et al, 2009(Zhang et al, , 2015bZhang & Fritsch, 2010)、白刺属 (Temirbayeva & Zhang, 2015;Zhang et al, 2015a)、木蓼属 (Atraphaxis) (Zhang et al, 2014b) 、红砂属 (Reaumuria) (Zhang et al, 2014a …”

Section: 属的研究论述了蒙古植物区系的过渡性质和东亚unclassified

A review on the floristic phytogeography in arid northwestern China and Central Asia

Zhang¹

2017

Biodiversity Science

View full text Add to dashboard Cite

Molecular phylogenetic and biogeographical analysis of Nitraria based on nuclear and chloroplast DNA sequences

Cited by 26 publications

References 38 publications

Molecular phylogenetics and molecular clock dating of Sapindales based on plastid rbcL, atpB and trnL-trnF DNA sequences

Molecular phylogenetics and molecular clock dating of Sapindales based on plastid rbcL, atpB and trnL-trnF DNA sequences

Himalayan uplift shaped biomes in Miocene temperate Asia: evidence from leguminous Caragana

A review on the floristic phytogeography in arid northwestern China and Central Asia

Contact Info

Product

Resources

About