×
验证码:
换一张
Forgotten Password?
Stay signed in
×
Log In
Chinese
|
English
中国科学院昆明植物研究所知识管理系统
Knowledge Management System of Kunming Institute of Botany,CAS
Log In
Register
ALL
ORCID
Title
Creator
Subject Area
Keyword
Funding Project
Document Type
Source Publication
Indexed By
Publisher
Date Issued
Date Accessioned
MOST Discipline Catalogue
Study Hall
Image search
Paste the image URL
Home
Collections
Authors
DocType
Subjects
K-Map
News
Search in the results
Collection
昆明植物所硕博研究... [40]
共享文献 [16]
中国科学院东亚植物... [14]
植物化学与西部植物... [11]
中国西南野生生物种质... [5]
云南植物研究 [3]
More...
Authors
李德铢 [8]
王红 [6]
许刚 [5]
Sun Hang [4]
伊廷双 [4]
郝小江 [3]
More...
Document Type
Journal a... [65]
Thesis [40]
Book [3]
Date Issued
2023 [4]
2021 [2]
2020 [8]
2019 [14]
2018 [9]
2017 [4]
More...
Language
英语 [39]
中文 [34]
Source Publication
云南植物研究 [5]
PHYTOCHEMI... [4]
植物分类与资源学报 [4]
JOURNAL OF... [3]
JOURNAL OF... [2]
JOURNAL OF... [2]
More...
Funding Project
GST, p < 0.01). At the regional level, Chinese and Japanese L. hodgsonii had a similar estimate of genetic diversity (China: Hd = 0.847, HT = 0.869; Japan: Hd = 0.766, HT = 0.867). Populations from China and Japan possess unique sets of haplotypes, and no haplotypes were shared between the regions. Furthermore, both the phyloegenetic and network analyses recovered the haplotypes of China and Japan as two distinct clades. Thus, we suggested the disjunct distribution of L. hodgsonii in China and Japan may present the climatic vicariant relicts of the ancient widely distributed populations. After divergence, this species within each region experienced independent evolutionary process. In China, L. hodgsonii was distributed around the Sichuan Basin. This distribution range can be divided into five regions. They were Jiajin Mountain region, E’mei Mountain region, Yunnan-Guizhou Plateau region, Wushan-Wuling Mountain region and Qinling Mountain region. Twelve haplotypes were indentified within these regions. Each region had its own specific haplotypes, which had different ancestry in the network. We deduced that Chinese L. hodgsonii might survive the LGM in multiple isolated refugia around the Sichuan Basin. In Japan, L. hodgsonii was disjunctively distributed in northern Honshu and Hokkaido. Seven haplotypes were identified within this region. However, the genetic diversity in Honshu (Hd = 0.821) was much higher than that in Hokkaido (Hd = 0.513). And all haplotypes in Hokkaido were derived from Honshu. This haplotype distribution suggested that the northern Honshu could have served as refuge in Japan. Nested clade analysis (NCA) indicated multiple forces including the vicariance and long-distance dispersal affected the disjunctive distribution among populations of L. hodgsonii in Japan.2. The phylogeography of L. tongolensis,Ligularia tongolensis was distributed along the Jinshajiang watershed, Yalongjiang watershed and Wumeng Mountain. In order to deduce the demographic history of this species, we sequenced two chloroplast DNA (cpDNA) intergenic spacers (trnQ-5’rps16, trnL-rpl32) in 140 individuals from 14 populations of three groups (Jinshajiang vs. Yalongjiang vs. Wumeng) within this species range. High levels of haplotype diversity (Hd = 0.814) and total genetic diversity (HT = 0.862) were detected at the species level, based on a total oftwelve haplotypes identified. However, the intrapopulation diversity (HS = 0.349) was low, which led to the high levels of genetic divergence (GST = 0.595, NST = 0.614, FST = 0.597). In consideration of the speciation of L. tongolensis resulting from the uplifts of the Qinghai-Tibetan Plateau (QTP), we thought the present genetic structure of L. tongolensis was shaped by the fragmentation of ancestral populations during the courses of QTP uplifts. This was further supported by the absence of IBD tests (r = –0.291, p = 0.964), which suggest that the differentiation had not occurred in accordance with the isolation by distance model. The genetic differentiation in L. tongolensis appears to be associated with historical events. Meanwhile, H2 and H5, the dominant haplotypes that located on internal nodes and deviated from extinct ancestral haplotype in the network, were detected to be shared between Jinshajiang and Yalongjiang groups. We deduced that ancestral populations of this species might have had a continuous distribution range, which was then fragmented and isolated by the following tectonic events. Finally, the ancestral polymorphism, H2 and H5, were randomly allocated in Jinshajiang watershed and Yalongjiang watershed. Meanwhile, H5 was the dominant haplotype in Jinshajiang watershed; H7 was the domiant haplotype in Yalongjiang watershed and Wumeng Mountain. This haplotype distribution pattern indicated that each group might have served as a refuge for L. tongolensis during the Quaternary Glaciation. Postglacial demographic expansion was supported by unimodal mismatch distribution and star-like phylogenies, with expansion ages of 274 ka B. P. for this species","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Hypericaceae&order=desc&&fq=dc.project.title_filter%3AThe%5C+origin%5C+center%5C+and%5C+diversity%5C+center%5C+of%5C+the%5C+genus%5C+Ligularia%5C+were%5C+considered%5C+to%5C+be%5C+central%5C+China%5C+and%5C+Hengduan%5C+Mountains%5C+Region%5C+%5C%28HMR%5C%29%5C+of%5C+China%2C%5C+respectively.%5C+In%5C+this%5C+research%2C%5C+we%5C+studied%5C+the%5C+phylogeographic%5C+pattern%5C+of%5C+L.%5C+hodgsonii%5C+and%5C+L.%5C+tongolensis%2C%5C+which%5C+was%5C+distributed%5C+in%5C+the%5C+origin%5C+center%5C+and%5C+diversity%5C+center%2C%5C+respectively.%5C+We%5C+aimed%5C+to%5C+infer%5C+the%5C+evolutionary%5C+process%5C+of%5C+Ligularia%5C+species.%5C+1.%5C+The%5C+phylogeography%5C+of%5C+L.%5C+hodgsonii%EF%BC%8CHere%2C%5C+we%5C+investigated%5C+the%5C+phylogeographic%5C+history%5C+of%5C+L.%5C+hodgsonii%5C+disjunctively%5C+distributed%5C+in%5C+China%5C+and%5C+Japan.%5C+Two%5C+hundred%5C+and%5C+eighty%5C+individuals%5C+were%5C+collected%5C+from%5C+29%5C+natural%5C+populations%2C%5C+23%5C+located%5C+in%5C+China%5C+and%5C+6%5C+in%5C+Japan.%5C+A%5C+total%5C+of%5C+19%5C+haplotypes%5C+were%5C+identified%5C+with%5C+the%5C+combination%5C+of%5C+three%5C+chloroplast%5C+DNA%5C+%5C%28cpDNA%5C%29%5C+sequences%5C+variations%5C+%5C%28trnQ%5C-5%E2%80%99rps16%2C%5C+trnL%5C-rpl32%5C+and%5C+psbA%5C-trnH%5C%29.%5C+At%5C+the%5C+species%5C+level%2C%5C+a%5C+high%5C+level%5C+of%5C+haplotype%5C+diversity%5C+%5C%28Hd%5C%29%5C+and%C2%A0total%5C+genetic%5C+diversity%5C+%5C%28HT%5C%29%5C+was%5C+detected.%5C+However%2C%5C+the%5C+average%5C+intrapopulation%5C+diversity%5C+%5C%28HS%5C%29%5C+was%5C+very%5C+low.%5C+Consequently%2C%5C+the%5C+population%5C+differentiation%5C%28NST%5C+%3D%5C+0.989%2C%5C+GST%5C+%3D%5C+0.933%5C+%5C%29%5C+was%5C+pronounced%5C+with%5C+a%5C+significant%5C+phylogeographic%5C+structure%5C+%5C%28NST%5C+%3E%5C+GST%2C%5C+p%5C+%3C%5C+0.01%5C%29.%5C+At%5C+the%5C+regional%5C+level%2C%5C+Chinese%5C+and%5C+Japanese%5C+L.%5C+hodgsonii%5C+had%5C+a%5C+similar%5C+estimate%5C+of%5C+genetic%5C+diversity%5C+%5C%28China%5C%3A%5C+Hd%5C+%3D%5C+0.847%2C%5C+HT%5C+%3D%5C+0.869%5C%3B%5C+Japan%5C%3A%5C+Hd%5C+%3D%5C+0.766%2C%5C+HT%5C+%3D%5C+0.867%5C%29.%5C+Populations%5C+from%5C+China%5C+and%5C+Japan%5C+possess%5C+unique%5C+sets%5C+of%5C+haplotypes%2C%5C+and%5C+no%5C+haplotypes%5C+were%5C+shared%5C+between%5C+the%5C+regions.%5C+Furthermore%2C%5C+both%5C+the%5C+phyloegenetic%5C+and%5C+network%5C+analyses%5C+recovered%5C+the%5C+haplotypes%5C+of%5C+China%5C+and%5C+Japan%5C+as%5C+two%5C+distinct%5C+clades.%5C+Thus%2C%5C+we%5C+suggested%5C+the%5C+disjunct%5C+distribution%5C+of%5C+L.%5C+hodgsonii%5C+in%5C+China%5C+and%5C+Japan%5C+may%5C+present%5C+the%5C+climatic%5C+vicariant%5C+relicts%5C+of%5C+the%5C+ancient%5C+widely%5C+distributed%5C+populations.%5C+After%5C+divergence%2C%5C+this%5C+species%5C+within%5C+each%5C+region%5C+experienced%5C+independent%5C+evolutionary%5C+process.%5C+In%5C+China%2C%5C+L.%5C+hodgsonii%5C+was%5C+distributed%5C+around%5C+the%5C+Sichuan%5C+Basin.%5C+This%5C+distribution%5C+range%5C+can%5C+be%5C+divided%5C+into%5C+five%5C+regions.%5C+They%5C+were%5C+Jiajin%5C+Mountain%5C+region%2C%5C+E%E2%80%99mei%5C+Mountain%5C+region%2C%5C+Yunnan%5C-Guizhou%5C+Plateau%5C+region%2C%5C+Wushan%5C-Wuling%5C+Mountain%5C+region%5C+and%5C+Qinling%5C+Mountain%5C+region.%5C+Twelve%5C+haplotypes%5C+were%5C+indentified%5C+within%5C+these%5C+regions.%5C+Each%5C+region%5C+had%5C+its%5C+own%5C+specific%5C+haplotypes%2C%5C+which%5C+had%5C+different%5C+ancestry%5C+in%5C+the%5C+network.%5C+We%5C+deduced%5C+that%5C+Chinese%5C+L.%5C+hodgsonii%5C+might%5C+survive%5C+the%5C+LGM%5C+in%5C+multiple%5C+isolated%5C+refugia%5C+around%5C+the%5C+Sichuan%5C+Basin.%5C+In%5C+Japan%2C%5C+L.%5C+hodgsonii%5C+was%5C+disjunctively%5C+distributed%5C+in%5C+northern%5C+Honshu%5C+and%5C+Hokkaido.%5C+Seven%5C+haplotypes%5C+were%5C+identified%5C+within%5C+this%5C+region.%5C+However%2C%5C+the%5C+genetic%5C+diversity%5C+in%5C+Honshu%5C+%5C%28Hd%5C+%3D%5C+0.821%5C%29%5C+was%5C+much%5C+higher%5C+than%5C+that%5C+in%5C+Hokkaido%5C+%5C%28Hd%5C+%3D%5C+0.513%5C%29.%5C+And%5C+all%5C+haplotypes%5C+in%5C+Hokkaido%5C+were%5C+derived%5C+from%5C+Honshu.%5C+This%5C+haplotype%5C+distribution%5C+suggested%5C+that%5C+the%5C+northern%5C+Honshu%5C+could%5C+have%5C+served%5C+as%5C+refuge%5C+in%5C+Japan.%5C+Nested%5C+clade%5C+analysis%5C+%5C%28NCA%5C%29%5C+indicated%5C+multiple%5C+forces%5C+including%5C+the%5C+vicariance%5C+and%5C+long%5C-distance%5C+dispersal%5C+affected%5C+the%5C+disjunctive%5C+distribution%5C+among%5C+populations%5C+of%5C+L.%5C+hodgsonii%5C+in%5C+Japan.2.%5C+The%5C+phylogeography%5C+of%5C+L.%5C+tongolensis%EF%BC%8CLigularia%5C+tongolensis%5C+was%5C+distributed%5C+along%5C+the%5C+Jinshajiang%5C+watershed%2C%5C+Yalongjiang%5C+watershed%5C+and%5C+Wumeng%5C+Mountain.%5C+In%5C+order%5C+to%5C+deduce%5C+the%5C+demographic%5C+history%5C+of%5C+this%5C+species%2C%5C+we%5C+sequenced%5C+two%5C+chloroplast%5C+DNA%5C+%5C%28cpDNA%5C%29%5C+intergenic%5C+spacers%5C+%5C%28trnQ%5C-5%E2%80%99rps16%2C%5C+trnL%5C-rpl32%5C%29%5C+in%5C+140%5C+individuals%5C+from%5C+14%5C+populations%5C+of%5C+three%5C+groups%5C+%5C%28Jinshajiang%5C+vs.%5C+Yalongjiang%5C+vs.%5C+Wumeng%5C%29%5C+within%5C+this%5C+species%5C+range.%5C+High%5C+levels%5C+of%5C+haplotype%5C+diversity%5C+%5C%28Hd%5C+%3D%5C+0.814%5C%29%5C+and%5C+total%5C+genetic%5C+diversity%5C+%5C%28HT%5C+%3D%5C+0.862%5C%29%5C+were%5C+detected%5C+at%5C+the%5C+species%5C+level%2C%5C+based%5C+on%5C+a%5C+total%5C+oftwelve%5C+haplotypes%5C+identified.%5C+However%2C%5C+the%5C+intrapopulation%5C+diversity%5C+%5C%28HS%5C+%3D%5C+0.349%5C%29%5C+was%5C+low%2C%5C+which%5C+led%5C+to%5C+the%5C+high%5C+levels%5C+of%5C+genetic%5C+divergence%5C+%5C%28GST%5C+%3D%5C+0.595%2C%5C+NST%5C+%3D%5C+0.614%2C%5C+FST%5C+%3D%5C+0.597%5C%29.%5C+In%5C+consideration%5C+of%5C+the%5C+speciation%5C+of%5C+L.%5C+tongolensis%5C+resulting%5C+from%5C+the%5C+uplifts%5C+of%5C+the%5C+Qinghai%5C-Tibetan%5C+Plateau%5C+%5C%28QTP%5C%29%2C%5C+we%5C+thought%5C+the%5C+present%5C+genetic%5C+structure%5C+of%5C+L.%5C+tongolensis%5C+was%5C+shaped%5C+by%5C+the%5C+fragmentation%5C+of%5C+ancestral%5C+populations%5C+during%5C+the%5C+courses%5C+of%5C+QTP%5C+uplifts.%5C+This%5C+was%5C+further%5C+supported%5C+by%5C+the%5C+absence%5C+of%5C+IBD%5C+tests%5C+%5C%28r%5C+%3D%5C+%E2%80%930.291%2C%5C+p%5C+%3D%5C+0.964%5C%29%2C%5C+which%5C+suggest%5C+that%5C+the%5C+differentiation%5C+had%5C+not%5C+occurred%5C+in%5C+accordance%5C+with%5C+the%5C+isolation%5C+by%5C+distance%5C+model.%5C+The%5C+genetic%5C+differentiation%5C+in%5C+L.%5C+tongolensis%5C+appears%5C+to%5C+be%5C+associated%5C+with%5C+historical%5C+events.%5C+Meanwhile%2C%5C+H2%5C+and%5C+H5%2C%5C+the%5C+dominant%5C+haplotypes%5C+that%5C+located%5C+on%5C+internal%5C+nodes%5C+and%5C+deviated%5C+from%5C+extinct%5C+ancestral%5C+haplotype%5C+in%5C+the%5C+network%2C%5C+were%5C+detected%5C+to%5C+be%5C+shared%5C+between%5C+Jinshajiang%5C+and%5C+Yalongjiang%5C+groups.%5C+We%5C+deduced%5C+that%5C+ancestral%5C+populations%5C+of%5C+this%5C+species%5C+might%5C+have%5C+had%5C+a%5C+continuous%5C+distribution%5C+range%2C%5C+which%5C+was%5C+then%5C+fragmented%5C+and%5C+isolated%5C+by%5C+the%5C+following%5C+tectonic%5C+events.%5C+Finally%2C%5C+the%5C+ancestral%5C+polymorphism%2C%5C+H2%5C+and%5C+H5%2C%5C+were%5C+randomly%5C+allocated%5C+in%5C+Jinshajiang%5C+watershed%5C+and%5C+Yalongjiang%5C+watershed.%5C+Meanwhile%2C%5C+H5%5C+was%5C+the%5C+dominant%5C+haplotype%5C+in%5C+Jinshajiang%5C+watershed%5C%3B%5C+H7%5C+was%5C+the%5C+domiant%5C+haplotype%5C+in%5C+Yalongjiang%5C+watershed%5C+and%5C+Wumeng%5C+Mountain.%5C+This%5C+haplotype%5C+distribution%5C+pattern%5C+indicated%5C+that%5C+each%5C+group%5C+might%5C+have%5C+served%5C+as%5C+a%5C+refuge%5C+for%5C+L.%5C+tongolensis%5C+during%5C+the%5C+Quaternary%5C+Glaciation.%5C+Postglacial%5C+demographic%5C+expansion%5C+was%5C+supported%5C+by%5C+unimodal%5C+mismatch%5C+distribution%5C+and%5C+star%5C-like%5C+phylogenies%2C%5C+with%5C+expansion%5C+ages%5C+of%5C+274%5C+ka%5C+B.%5C+P.%5C+for%5C+this%5C+species"},{"jsname":"Youth Innovation Promotion Association CAS[2016350]","jscount":"1","jsurl":"/simple-search?field1=all&rpp=10&accurate=false&advanced=false&sort_by=2&isNonaffiliated=false&search_type=-1&query1=Hypericaceae&order=desc&&fq=dc.project.title_filter%3AYouth%5C+Innovation%5C+Promotion%5C+Association%5C+CAS%5C%5B2016350%5C%5D"},{"jsname":"lastIndexed","jscount":"2024-12-12"}],"Funding Project","dc.project.title_filter")'>
CAS, Yunna... [1]
Keynote Pr... [1]
Kunming In... [1]
Major Inte... [1]
Mt. Jiaozi... [1]
National K... [1]
More...
Indexed By
SCI [33]
CSCD [6]
BSCI [1]
Funding Organization
China Scho... [2]
31590820) [1]
41571059) [1]
Applied Fu... [1]
CAS, Yunna... [1]
CGIAR rese... [1]
More...
×
Knowledge Map
KIB OpenIR
Start a Submission
Submissions
Unclaimed
Claimed
Attach Fulltext
Bookmarks
QQ
Weibo
Feedback
Browse/Search Results:
1-10 of 108
Help
Selected(
0
)
Clear
Items/Page:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
Sort:
Select
Submit date Ascending
Submit date Descending
Author Ascending
Author Descending
Journal Impact Factor Ascending
Journal Impact Factor Descending
Title Ascending
Title Descending
WOS Cited Times Ascending
WOS Cited Times Descending
Issue Date Ascending
Issue Date Descending
Systema Angiospermarum
期刊论文
出版物, 3111, 页码: 1—21
Authors:
Zuo Z(作者)
Adobe PDF(146Kb)
  |  
Favorite
  |  
View/Download:252/2
  |  
Submit date:2017/07/19
Seed morphology of Hypericum (Hypericaceae) in China and its taxonomic significance
期刊论文
MICROSCOPY RESEARCH AND TECHNIQUE, 2023
Authors:
Bai,Rui-Zhu
;
Zhao,Fei
;
Drew,Bryan T.
;
Xu,Gang
;
Cai,Jie
;
Shen,Shi-Kang
;
Xiang,Chun-Lei
View
  |  
Adobe PDF(3815Kb)
  |  
Favorite
  |  
View/Download:55/14
  |  
Submit date:2024/07/10
Hypericeae
Malpighiales
micromorphology
seed surface ornamentation
taxonomy
ST-JOHNS-WORT
MOLECULAR PHYLOGENETICS
SYSTEMATIC SIGNIFICANCE
MICROMORPHOLOGY
CHARACTERS
DEPRESSION
EVOLUTION
Structurally diverse spirocyclic polycyclic polyprenylated acylphloroglucinols from Hypericum ascyron Linn. and their anti-tumor activity
期刊论文
PHYTOCHEMISTRY, 2023, 卷号: 212, 页码: 113727
Authors:
Hu,Ya-Li
;
Yue,Grace Gar-Lee
;
Li,Xing-Ren
;
Xu,Gang
;
Lau,Clara Bik-San
View
  |  
Adobe PDF(6872Kb)
  |  
Favorite
  |  
View/Download:47/15
  |  
Submit date:2024/07/25
Hypericaceae
Polycyclic polyprenylated acylphloroglucinols
Spirocyclic polyprenylated acylphloroglucinols
HCT116 cells
Zebrafish model
Hypericum ascyron Linn
NATURAL-PRODUCTS
A-H
DERIVATIVES
FLOWERS
VEGF
Pleomorphic Dematiomelanomma yunnanense gen. et sp. nov. (Ascomycota, Melanommataceae) from grassland vegetation in Yunnan, China
期刊论文
MYCOKEYS, 2023, 期号: 98, 页码: 273-297
Authors:
Gao,Ying
;
Zhong,Tingfang
;
Bhat,Jayarama D.
;
de Farias,Antonio Roberto Gomes
;
Dawoud,Turki M.
;
Hyde,Kevin D.
;
Xiong,Weiqiang
;
Li,Yunju
;
Gui,Heng
;
Yang,Xuefei
;
Wu,Shixi
;
Wanasinghe,Dhanushka N.
View
  |  
Adobe PDF(5684Kb)
  |  
Favorite
  |  
View/Download:104/20
  |  
Submit date:2024/05/09
Asexual morph
Greater Mekong Subregion
molecular phylogeny
muriform
Pleosporales
sexual morph
taxonomy
MULTIPLE SEQUENCE ALIGNMENT
MICROCYCLE CONIDIATION
FUNGI
NAMES
TAXA
PLEOSPORALES
REVISION
PETRAKIA
RECORDS
CHOICE
Hypericum podocarpoides N. Robson (Hypericaceae): a newly recorded species from China
期刊论文
Plant Science Journal, 2023, 卷号: 41, 期号: 1, 页码: 1-6 2095-0837(2023)41:1<1:HPNRHA>2.0.TX;2-I
Authors:
Bai RZ(白蕊珠)
;
Zhao F(赵飞)
;
Cai J(蔡杰)
;
Shen SK(申仕康)
;
Xiang CL(向春雷)
View
  |  
Adobe PDF(345Kb)
  |  
Favorite
  |  
View/Download:23/10
  |  
Submit date:2024/07/30
Chemical constituents from the flowers of Hypericum monogynum L. with COX-2 inhibitory activity
期刊论文
PHYTOCHEMISTRY, 2022, 卷号: 193, 页码: 112970
Authors:
Li,Ya-Nan
;
Zeng,Yan-Rong
;
Yang,Jue
;
He,Wenwen
;
Chen,Junlei
;
Deng,Lulu
;
Yi,Ping
;
Huang,Lie-Jun
;
Gu,Wei
;
Hu,Zhan-Xing
;
Yuan,Chun-Mao
;
Hao,Xiao-Jiang
Favorite
  |  
View/Download:160/0
  |  
Submit date:2022/04/02
Hypericum monogynum L.
Hypericaceae
Chemical constituents
Polycyclic polyprenylated acylphloroglucinols
Flavonoids
COX-2 inhibitors
Diversity of Flower Visiting Beetles at Higher Elevations on the Yulong Snow Mountain (Yunnan, China)
期刊论文
DIVERSITY-BASEL, 2021, 卷号: 13, 期号: 11, 页码: 604
Authors:
Li,Kai-Qin
;
Ren,Zong-Xin
;
Li,Qiang
View
  |  
Adobe PDF(2409Kb)
  |  
Favorite
  |  
View/Download:182/57
  |  
Submit date:2022/04/02
alpine
diversity
Hengduan Mountain
modularity
plant-insect interaction
FLORAL BIOLOGY
RAIN-FOREST
POLLINATION
COLEOPTERA
COMMUNITY
SPECIALIZATION
NETWORKS
SARAWAK
ANDES
Phylogenetic patterns suggest frequent multiple origins of secondary metabolites across the seed-plant 'tree of life'
期刊论文
NATIONAL SCIENCE REVIEW, 2021
Authors:
Zhang,Yongzeng
;
Deng,Tao
;
Sun,Lu
;
Landis,Jacob B.
;
Moore,Michael J.
;
Wang,Hengchang
;
Wang,Yuehua
;
Hao,Xiaojiang
;
Chen,Jijun
;
Li,Shenghong
;
Xu,Maonian
;
Puno,Pema-Tenzin
;
Raven,Peter H.
;
Sun,Hang
View
  |  
Adobe PDF(1313Kb)
  |  
Favorite
  |  
View/Download:241/41
  |  
Submit date:2023/09/08
被子植物叶绿体系统发育基因组学研究
学位论文
, 2020
Authors:
甘露
Adobe PDF(11879Kb)
  |  
Favorite
  |  
View/Download:282/1
  |  
Submit date:2023/11/02
异戊烯基芳香天然产物发现及其 核磁规律和生物合成研究
学位论文
, 2020
Authors:
任福才
Adobe PDF(4272Kb)
  |  
Favorite
  |  
View/Download:228/1
  |  
Submit date:2023/11/02