Clarkia unguiculata - Unknown
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Internal ID UUID6440119c305fc701251005
Scientific name Clarkia unguiculata
Authority Lindl.
First published in Edwards's Bot. Reg. 23: t. 1981 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oenothera elegans E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 9: 191 (1901)
Phaeostoma douglasii Spach Hist. Nat. Vég. 4: 393 (1835)
Clarkia eiseneana Kellogg Proc. Calif. Acad. Sci. 7: 94 (1877)
Clarkia elegans Douglas ex Lindl. Edwards's Bot. Reg. 19: t. 1575. 1833
Phaeostoma elegans A.Nelson Bot. Gaz. 52: 267. 1911

Common names Top

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Language Common/alternative name
English elegant clarkia
Bengali এলিগেন্ট ক্লারকিয়া
Czech lokanka lepá
Welsh clarcia
Finnish komeasilkkikukka
Upper Sorbian mandlowa róža
Norwegian Bokmål hageklarkia
Polish klarkia wytworna
Chinese 有爪仙女扇
Chinese 有爪克拉花

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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • South European Russia
    • Middle Europe
      • Czechoslovakia
    • Northern Europe
      • Denmark
      • Finland
      • Norway
      • Sweden
  • Northern America
    • Mexico
      • Mexico Northwest
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000608599
USDA Plants CLUN
Tropicos 23200769
INPN 91834
KEW urn:lsid:ipni.org:names:611540-1
The Plant List kew-2724731
Open Tree Of Life 1015485
NCBI Taxonomy 3937
NBN Atlas NHMSYS0000457369
Nature Serve 2.136056
IPNI 611540-1
iNaturalist 51735
GBIF 5420957
Freebase /m/03h1fj9
EPPO CKAUN
EOL 585428
Calflora (Californian flora) 2224
USDA GRIN 310108
Wikipedia Clarkia_unguiculata
CMAUP NPO18404

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
The extent of introgression between incipient Clarkia species is determined by temporal environmental variation and mating system Sianta SA, Moeller DA, Brandvain Y Proc Natl Acad Sci U S A 11-Mar-2024
PMCID:PMC10963018
doi:10.1073/pnas.2316008121
PMID:38466849
Gametic selection favours polyandry and selfing Scott MF, Mackintosh C, Immler S PLoS Genet 16-Feb-2024
PMCID:PMC10903963
doi:10.1371/journal.pgen.1010660
PMID:38363804
Abstracts of the papers presented in the international conference of Indian Virological Society, VIROCON 2022 on “Emerging and re-emerging viral infections impacting humans, animals, plants, fish and environment” held during 05–06 November, 2022 at Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir (SKUAST-K), Srinagar (J&K), India N/A Virusdisease 21-Mar-2023
PMCID:PMC10028750
doi:10.1007/s13337-023-00811-4
Flowering Mechanisms and Environmental Stimuli for Flower Transition: Bases for Production Scheduling in Greenhouse Floriculture Proietti S, Scariot V, De Pascale S, Paradiso R Plants (Basel) 05-Feb-2022
PMCID:PMC8839403
doi:10.3390/plants11030432
PMID:35161415
Genetic basis and dual adaptive role of floral pigmentation in sunflowers Todesco M, Bercovich N, Kim A, Imerovski I, Owens GL, Dorado Ruiz Ó, Holalu SV, Madilao LL, Jahani M, Légaré JS, Blackman BK, Rieseberg LH eLife 18-Jan-2022
PMCID:PMC8765750
doi:10.7554/eLife.72072
PMID:35040432
Diversity, phylogeny and evolution of the rapidly evolving genus Psidium L. (Myrtaceae, Myrteae) Proença CE, Tuler AC, Lucas EJ, Vasconcelos TN, de Faria JE, Staggemeier VG, de-Carvalho PS, Forni-Martins ER, Inglis PW, da Mata LR, da Costa IR Ann Bot 16-Jan-2022
PMCID:PMC8944734
doi:10.1093/aob/mcac005
PMID:35034117
Interactions of Coated-Gold Engineered Nanoparticles with Aquatic Higher Plant Salvinia minima Baker Mahaye N, Thwala M, Musee N Nanomaterials (Basel) 24-Nov-2021
PMCID:PMC8704737
doi:10.3390/nano11123178
PMID:34947527
Editorial: The Role of Flower Color in Angiosperm Evolution Narbona E, Arista M, Whittall JB, Camargo MG, Shrestha M Front Plant Sci 17-Sep-2021
PMCID:PMC8484755
doi:10.3389/fpls.2021.736998
PMID:34603361
Abiotic Environment Predicts Micro- but Not Macroevolutionary Patterns of Flower Color in Monkeyflowers (Phrymaceae) Grossenbacher D, Makler L, McCarthy M, Fraga N Front Plant Sci 25-Mar-2021
PMCID:PMC8030662
doi:10.3389/fpls.2021.636133
PMID:33841464
Darwin's vexing contrivance: a new hypothesis for why some flowers have two kinds of anther Kay KM, Jogesh T, Tataru D, Akiba S Proc Biol Sci 23-Dec-2020
PMCID:PMC7779490
doi:10.1098/rspb.2020.2593
PMID:33352073
Climate Predicts UV Floral Pattern Size, Anthocyanin Concentration, and Pollen Performance in Clarkia unguiculata Peach K, Liu JW, Mazer SJ Front Plant Sci 16-Jun-2020
PMCID:PMC7308548
doi:10.3389/fpls.2020.00847
PMID:32612627
Sex‐specific floral attraction traits in a sequentially hermaphroditic species Peach K, Liu JW, Klitgaard KN, Mazer SJ Ecol Evol 05-Feb-2020
PMCID:PMC7042773
doi:10.1002/ece3.5987
PMID:32128121
Plant speciation in the age of climate change Levin DA Ann Bot 28-Jun-2019
PMCID:PMC6868396
doi:10.1093/aob/mcz108
PMID:31250895
Decades of native bee biodiversity surveys at Pinnacles National Park highlight the importance of monitoring natural areas over time Meiners JM, Griswold TL, Carril OM PLoS One 17-Jan-2019
PMCID:PMC6336250
doi:10.1371/journal.pone.0207566
PMID:30653514
Pollen precedence in sexual Potentilla puberula and its role as a protective reproductive barrier against apomictic cytotypes Alonso-Marcos H, Hülber K, Myllynen T, Rodríguez PP, Dobeš C Taxon 01-Dec-2018
PMCID:PMC6368848
doi:10.12705/676.9
PMID:30745710

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 / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(23S)-1beta-[[2-O-[3-O-(beta-D-Glucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyl]oxy]-23-(beta-D-glucopyranosyloxy)spirosta-5,25(27)-diene-3beta-ol 10581939 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19C(CC(=C)CO9)OC1C(C(C(C(O1)CO)O)O)O 1047.10 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 100982641 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 754.90 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 44575746 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 708.90 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
[(3S,4S,5R,6S)-5-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl] acetate 101937241 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 911.00 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside 91936850 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC1(CCC(=C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C 254.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database

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