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Aquilegia flabellata

Aquilegia flabellata - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644009ef9967d516242687
Scientific name Aquilegia flabellata
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 183 (1845)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aquilegia akitensis Huth Bull. Herb. Boissier 5: 1090 (1897)
Aquilegia akitensis var. globularis Honda & Kishinami Bot. Mag. (Tokyo) 47: 434 1933
Aquilegia amurensis Kom. Bot. Mater. Gerb. Glavn. Bot. Sada S.S.S.R. 6: 8 (1926)
Aquilegia buergeriana var. pumila Huth Bull. Herb. Boissier 5: 1090 1897
Aquilegia fauriei H.Lév. Bull. Acad. Int. Géogr. Bot. sér. 3, 11(156): 300. 1902 [Nov 1902]
Aquilegia fauriei H.Lév. & Vaniot Bull. Acad. Int. Géogr. Bot. 11: 300 (1902)
Aquilegia flabellata var. alpina Kuzen. Izv. Imp. Akad. Nauk VI, 5: 4 1915
Aquilegia flabellata var. humiliata Makino Bot. Mag. (Tokyo) 24: 141 1910
Aquilegia flabellata var. protypica Takeda Alpine Fl. Japan 4 1938
Aquilegia flabellata f. pumila (Huth) Kudô Rep. Veg. N. Saghal. 129 1924
Aquilegia flabellata var. pumila (Huth) Kudô Rep. Exped. For. Kyushu Imp. Univ. 1: 65 1931
Aquilegia glandulosa Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 8. 1867
Aquilegia japonica f. globularis Nakai & Hara Bot. Mag. (Tokyo) 49: 7 1935
Aquilegia sibirica var. flabellata Finet & Gagnep. Bull. Soc. Bot. France 51: 412 1904
Aquilegia sibirica var. japonica Rapaics Bot. Közlem. 8: 134 1909
Aquilegia sibirica var. spectabilis Baker Gard. Chron. n.s., 10: 111 1878
Aquilegia spectabilis Lem. Ill. Hort. 11: t. 403 (1864)

Common names Top

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Language Common/alternative name
English fan columbine
Arabic أنقولية مروحية
Finnish japaninakileija
Japanese ミヤマオダマキ
Polish orlik wachlarzowaty
Swedish japansk akleja
Chinese 白山耧斗菜
Chinese 扇形耧斗菜
Chinese 深山苧環

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000541311
USDA Plants AQFL2
Tropicos 27102316
KEW urn:lsid:ipni.org:names:708885-1
The Plant List kew-2644771
Missouri Botanical Garden 286247
Open Tree Of Life 18889
Observations.org 125344
NCBI Taxonomy 291305
IPNI 708885-1
iNaturalist 509390
GBIF 3931157
Freebase /m/0ktpj26
EPPO AQIFL
EOL 2880044
USDA GRIN 3746
Wikipedia Aquilegia_flabellata

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Current state of populations of Rhodiola rosea L. (Crassulaceae) in East Kazakhstan Kubentayev SA, Zhumagul MZ, Kurmanbayeva MS, Alibekov DT, Kotukhov JA, Sitpayeva GT, Mukhtubayeva SK, Izbastina KS Bot Stud 07-Nov-2021
PMCID:PMC8572951
doi:10.1186/s40529-021-00327-4
PMID:34746988
The timetable for allopolyploidy in flowering plants Levin DA Ann Bot 21-Aug-2013
PMCID:PMC3806526
doi:10.1093/aob/mct194
PMID:23965616
Widespread Endogenization of Genome Sequences of Non-Retroviral RNA Viruses into Plant Genomes Chiba S, Kondo H, Tani A, Saisho D, Sakamoto W, Kanematsu S, Suzuki N PLoS Pathog 14-Jul-2011
PMCID:PMC3136472
doi:10.1371/journal.ppat.1002146
PMID:21779172
Aquilegia as a model system for the evolution and ecology of petals Kramer EM, Hodges SA Philos Trans R Soc Lond B Biol Sci 12-Feb-2010
PMCID:PMC2838260
doi:10.1098/rstb.2009.0230
PMID:20047874
Adaptive radiations: From field to genomic studies Hodges SA, Derieg NJ Proc Natl Acad Sci U S A 15-Jun-2009
PMCID:PMC2702792
doi:10.1073/pnas.0901594106
PMID:19528644
Dormancy of alpine and subalpine perennial forbs Yoshie F Ecol Res 08-Feb-2007
PMCID:PMC7159367
doi:10.1007/s11284-007-0334-7
PMID:32313370
Phylogenetic Variation in the Silicon Composition of Plants HODSON MJ, WHITE PJ, MEAD A, BROADLEY MR Ann Bot 21-Sep-2005
PMCID:PMC4247092
doi:10.1093/aob/mci255
PMID:16176944
Cycloartane-type glycosides from Aquilegia flabellata. Yoshimitsu H, Nishidas M, Hashimoto F, Nohara T Phytochemistry 01-Jun-1999
doi:10.1016/S0031-9422(98)00735-3
PMID:10438199

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives / Withanolide glycosides and derivatives
(2S)-2-[(1S)-1-[(1S,3R,6S,7R,8R,11S,12S,14R,15R,16R)-6-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162973317 Click to see CC1=CCC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)O 943.10 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
(2S)-2-[(1S)-1-[(1S,3R,6S,7R,8R,11S,12S,14R,15R,16R)-6-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162925427 Click to see CC1=CCC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)O 780.90 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
(2S)-2-[(1S)-1-[(1S,3R,6S,7R,8R,11S,12S,14R,15R,16R)-6-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,5-dihydropyran-6-one 100978846 Click to see CC1C=CC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)O 780.90 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
(2S)-2-[(1S)-1-[(1S,3R,6S,7R,8R,11S,12S,14R,15R,16R)-6-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 163190434 Click to see CC1=CCC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)O 943.10 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
(2S)-2-[(1S)-1-[(1S,3R,6S,7R,8R,11S,12S,14R,15R,16R)-6-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,5-dihydropyran-6-one 100978845 Click to see CC1C=CC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)O 943.10 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
2-[1-[6-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162925426 Click to see CC1=CCC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)O 780.90 unknown https://doi.org/10.1016/S0031-9422(98)00735-3
2-[1-[6-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162973315 Click to see CC1=CCC(OC1=O)C(C)C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)CO)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)O 943.10 unknown https://doi.org/10.1016/S0031-9422(98)00735-3

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