Qiaoping Xiang

Dr. Qiaoping Xiang


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 June 2017 in Genome Biology and Evolution
Verified
Journal Article
Open access
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RWRan Wei
Ran Wei
YYYue-Hong Yan
Yue-Hong Yan
AHAj Harris
Aj Harris
JKJong-Soo Kang
Jong-Soo Kang
HSHui Shen
Hui Shen
XZXian-Chun Zhang
Xian-Chun Zhang
The eupolypods II ferns represent a classic case of evolutionary radiation and, simultaneously, exhibit high substitution rate heterogeneity. These factors have been proposed to contribute to the contentious resolutions among clades within this fern group in multilocus phylogenetic studies. We investigated the deep phylogenetic relationships of eupolypod II ferns by sampling all major families and using 40 plastid genomes, or plastomes, of which 33 were newly sequenced with next-generation sequencing technology. We performed model-based analyses to evaluate the diversity of molecular evolutionary rates for these ferns. Our plastome data, with more than 26,000 informative characters, yielded good resolution for deep relationships within eupolypods II and unambiguously clarified the position of Rhachidosoraceae and the monophyly of Athyriaceae. Results of rate heterogeneity analysis revealed approximately 33 significant rate shifts in eupolypod II ferns, with the most heterogeneous rates (both accelerations and decelerations) occurring in two phylogenetically difficult lineages, that is, the Rhachidosoraceae–Aspleniaceae and Athyriaceae clades. These observations support the hypothesis that rate heterogeneity has previously constrained the deep phylogenetic resolution in eupolypods II. According to the plastome data, we propose that 14 chloroplast markers are particularly phylogenetically informative for eupolypods II both at the familial and generic levels. Our study demonstrates the power of a character-rich plastome data set and high-throughput sequencing for resolving the recalcitrant lineages, which have undergone rapid evolutionary radiation and dramatic changes in substitution rates.

19 October 2020 in The Plant Journal
Verified
Journal Article
Closed access
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JKJong‐Soo Kang
Jong‐Soo Kang
HZHong‐Rui Zhang
Hong‐Rui Zhang
YWYa‐Rong Wang
Ya‐Rong Wang
SLSi‐Qi Liang
Si‐Qi Liang
ZMZhi‐Yuan Mao
Zhi‐Yuan Mao
QXQiaoping Xiang
Qiaoping Xiang

9 November 2012 in BMC Plant Biology
Verified
Journal Article
Open access
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LWLi Wang
Li Wang
HLHongmei Liu
Hongmei Liu
Xian-Chun ZhangXian-Chun Zhang
Xian-Chun Zhang
QXQiaoping Xiang
Qiaoping Xiang
Background: The rise of high mountain chains is widely seen as one of the factors driving rapid diversification of land plants and the formation of biodiversity hotspots. Supporting evidence was reported for the impact of the rapid rise of the Andean mountains but this hypothesis has so far been less explored for the impact of the “roof of the world”. The formation of the Himalaya, and especially the rise of the Qinghai–Tibetan Plateau in the recent 20 million years, altered the monsoon regimes that dominate the current climates of South East Asia. Here, we infer the hypothesis that the rise of Himalaya had a strong impact on the plant diversity in the biodiversity hotspot of the Southwest Chinese Mountains. Results: Our analyses of the diversification pattern of the derived fern genus Lepisorus recovered evidence for changes in plant diversity that correlated with the strengthening of South East Asian monsoon. Southwest China or Southwest China and Japan was recovered as the putative area of origin of Lepisorus and enhancing monsoon regime were found to shape the early diversification of the genus as well as subsequent radiations during the late Miocene and Pliocene. Conclusions: We report new evidence for a coincidence of plant diversification and changes of the climate caused by the uplift of the Himalaya. These results are discussed in the context of the impact of incomplete taxon sampling, uncertainty of divergence time estimates, and limitations of current methods used to assess diversification rates.

1 January 2015 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
QXQiaoping Xiang
Qiaoping Xiang
RWRan Wei
Ran Wei
YSYi-Zhen Shao
Yi-Zhen Shao
ZYZu-Yu Yang
Zu-Yu Yang
XWXiao-Quan Wang
Xiao-Quan Wang
XZXian-Chun Zhang
Xian-Chun Zhang

1 April 2019 in Genome Biology and Evolution
Verified
Journal Article
Open access
PDF file
HZHong-Rui Zhang
Hong-Rui Zhang
QXQiaoping Xiang
Qiaoping Xiang
Xian-Chun ZhangXian-Chun Zhang
Xian-Chun Zhang
Both direct repeats (DR) and inverted repeats (IR) are documented in the published plastomes of Selaginella species indicating the unusual and diverse plastome structure in the family Selaginellaceae. In this study, we newly sequenced complete plastomes of seven species from five main lineages of Selaginellaceae and also resequenced three species (Selaginella tamariscina, Selaginella uncinata, and Selaginella moellendorffii) to explore the evolutionary trajectory of Selaginellaceae plastomes. Our results showed that the plastomes of Selaginellaceae vary remarkably in size, gene contents, gene order, and GC contents. Notably, both DR and IR structures existed in the plastomes of Selaginellaceae with DR structure being an ancestral state. The occurrence of DR structure was at ∼257 Ma and remained in most subgenera of Selaginellaceae, whereas IR structure only reoccurred in Selaginella sect. Lepidophyllae (∼143 Ma) and Selaginella subg. Heterostachys (∼19 Ma). The presence of a pair of large repeats psbK-trnQ, together with DR/IR region in Selaginella bisulcata, Selaginella pennata, S. uncinata, and Selaginella hainanensis, could frequently mediate diverse homologous recombination and create approximately equal stoichiometric isomers (IR/DR-coexisting) and subgenomes. High proportion of repeats is presumably responsible for the dynamic IR/DR-coexisting plastomes, which possess a lower synonymous substitution rate (dS) compared with DR-possessing and IR-possessing plastomes. We propose that the occurrence of DR structure, together with few repeats, is possibly selected to keep the stability of plastomes and the IR/DR-coexisting plastomes also reached an equilibrium in plastome organization through highly efficient homologous recombination to maintain stability.

31 January 2010 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
LWLi Wang
Li Wang
XQXin-Ping Qi
Xin-Ping Qi
QXQiaoping Xiang
Qiaoping Xiang
JHJochen Heinrichs
Jochen Heinrichs
HLHongmei Liu
Hongmei Liu
Xian-Chun ZhangXian-Chun Zhang
Xian-Chun Zhang