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Helianthus argophyllus

Helianthus argophyllus - Unknown
Part: Unknown
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 UUID643fd19c64818714513379
Scientific name Helianthus argophyllus
Authority Torr. & A.Gray
First published in Fl. N. Amer. 2(2): 318 [-319] (1842)

Description Top

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Helianthus argophyllus, also known as silverleaf sunflower, is a species of sunflower native to coastal regions of Texas in North America. It has also been naturalized in other places such as Florida, North Carolina, Argentina, Africa, and Australia. This annual herb can grow up to 300 cm tall and is characterized by its silvery appearance due to a coating of fine hairs on its leaves and stems. It produces 1-5 flower heads, each containing 15-20 ray florets and 150 or more disc florets. This plant is typically found in sandy areas near the coast.

Synonyms Top

Scientific name Authority First published in
Helianthus annuus var. argophyllus (Torr. & A.Gray) Anashch. Bot. Zhurn. (Moscow & Leningrad) 59: 1476 (1974)

Common names Top

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Language Common/alternative name
English silverleaf sunflower
Chinese 绢毛葵

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Kwazulu-Natal
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Florida
      • North Carolina

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000116726
Florida Plant Atlas 1668
USDA Plants HEAR3
Tropicos 2702630
KEW urn:lsid:ipni.org:names:119047-2
The Plant List gcc-7811
Open Tree Of Life 769540
NCBI Taxonomy 73275
NBN Atlas NHMSYS0000459274
Nature Serve 2.147465
IUCN Red List 20694242
IPNI 119047-2
iNaturalist 163609
GBIF 3119232
EPPO HELAR
EOL 491622
USDA GRIN 27924
Wikipedia Helianthus_argophyllus

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
Mitogenomic Research of Silverleaf Sunflower (Helianthus argophyllus) and Its Interspecific Hybrids Makarenko MS, Azarin KV, Gavrilova VA Curr Issues Mol Biol 02-Jun-2023
PMCID:PMC10297576
doi:10.3390/cimb45060308
PMID:37367057
Dispersal inference from population genetic variation using a convolutional neural network Smith CC, Tittes S, Ralph PL, Kern AD Genetics 13-Apr-2023
PMCID:PMC10213498
doi:10.1093/genetics/iyad068
PMID:37052957
The genomics of linkage drag in inbred lines of sunflower Huang K, Jahani M, Gouzy J, Legendre A, Carrere S, Lázaro-Guevara JM, González Segovia EG, Todesco M, Mayjonade B, Rodde N, Cauet S, Dufau I, Staton SE, Pouilly N, Boniface MC, Tapy C, Mangin B, Duhnen A, Gautier V, Poncet C, Donnadieu C, Mandel T, Hübner S, Burke JM, Vautrin S, Bellec A, Owens GL, Langlade N, Muños S, Rieseberg LH Proc Natl Acad Sci U S A 27-Mar-2023
PMCID:PMC10083583
doi:10.1073/pnas.2205783119
PMID:36972449
Re-evaluating Homoploid Reticulate Evolution in Helianthus Sunflowers Owens GL, Huang K, Todesco M, Rieseberg LH Mol Biol Evol 17-Jan-2023
PMCID:PMC9907532
doi:10.1093/molbev/msad013
PMID:36648104
HeliantHOME, a public and centralized database of phenotypic sunflower data Bercovich N, Genze N, Todesco M, Owens GL, Légaré JS, Huang K, Rieseberg LH, Grimm DG Sci Data 30-Nov-2022
PMCID:PMC9712528
doi:10.1038/s41597-022-01842-0
PMID:36450875
Mutation Load in Sunflower Inversions Is Negatively Correlated with Inversion Heterozygosity Huang K, Ostevik KL, Elphinstone C, Todesco M, Bercovich N, Owens GL, Rieseberg LH Mol Biol Evol 10-May-2022
PMCID:PMC9127631
doi:10.1093/molbev/msac101
PMID:35535689
The evolutionary and molecular features of the broad‐host‐range plant pathogen Sclerotinia sclerotiorum Derbyshire MC, Newman TE, Khentry Y, Owolabi Taiwo A Mol Plant Pathol 11-Apr-2022
PMCID:PMC9276942
doi:10.1111/mpp.13221
PMID:35411696
Host plants and pollination regions for the long‐distance migratory noctuid moth, Hadula trifolii Hufnagel in China He L, Liu Y, Guo J, Chang H, Wu K Ecol Evol 11-Apr-2022
PMCID:PMC9001116
doi:10.1002/ece3.8819
PMID:35432928
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
Genetic Improvement in Sunflower Breeding—Integrated Omics Approach Jocković M, Jocić S, Cvejić S, Marjanović-Jeromela A, Jocković J, Radanović A, Miladinović D Plants (Basel) 04-Jun-2021
PMCID:PMC8228292
doi:10.3390/plants10061150
PMID:34200113
Extremely low nucleotide diversity among thirty-six new chloroplast genome sequences from Aldama (Heliantheae, Asteraceae) and comparative chloroplast genomics analyses with closely related genera Loeuille B, Thode V, Siniscalchi C, Andrade S, Rossi M, Pirani JR PeerJ 24-Feb-2021
PMCID:PMC7912680
doi:10.7717/peerj.10886
PMID:33665028
Unraveling the Sclerotinia Basal Stalk Rot Resistance Derived From Wild Helianthus argophyllus Using a High-Density Single Nucleotide Polymorphism Linkage Map Talukder ZI, Underwood W, Misar CG, Seiler GJ, Liu Y, Li X, Cai X, Qi L Front Plant Sci 03-Feb-2021
PMCID:PMC7886805
doi:10.3389/fpls.2020.617920
PMID:33613588
High-Density Mapping and Candidate Gene Analysis of Pl18 and Pl20 in Sunflower by Whole-Genome Resequencing Ma G, Song Q, Li X, Qi L Int J Mol Sci 16-Dec-2020
PMCID:PMC7765508
doi:10.3390/ijms21249571
PMID:33339111
Heterotic Effect of Different Cytoplasmic Combinations in Sunflower Hybrids Cultivated Under Diverse Irrigation Regimes Tyagi V, Dhillon SK, Kaur G, Kaushik P Plants (Basel) 07-Apr-2020
PMCID:PMC7238153
doi:10.3390/plants9040465
PMID:32272619
Phylogeography and the Evolutionary History of Sunflower (Helianthus annuus L.): Wild Diversity and the Dynamics of Domestication Park B, Burke JM Genes (Basel) 29-Feb-2020
PMCID:PMC7140811
doi:10.3390/genes11030266
PMID:32121324

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,5R,9R,10S,13S,14R)-14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-5-carboxylic acid 163004418 Click to see CC12CCCC(C1CCC34C2C=CC(C3)C(C4)(C)O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(82)83171-3
(1S,4R,9R,10S,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 162952054 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(82)83171-3
Kauran-16-ol 623309 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(82)83171-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Arundinol C 71524403 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(C)(COC(=O)C)O 310.40 unknown https://doi.org/10.1016/0031-9422(82)83171-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2S,3S,5R,8E,11S)-2-hydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-8-en-13-one 163018269 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
2-Hydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-8-en-13-one 181707 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
Simsiolide 101967113 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/S0031-9422(00)94519-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 137706071 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
https://doi.org/10.1016/0305-1978(89)90094-X
(4-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-7-yl) acetate 162849534 Click to see CC1=CCC(C(=CC(C2C(C1)OC(=O)C2=C)O)C)OC(=O)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
(8-Hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl) 2-methylbut-2-enoate 162902025 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)C)O)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
(8,9-Dihydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl) 2-methylbut-2-enoate 435055 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)(C)O)O)C 380.40 unknown https://doi.org/10.1016/0031-9422(82)83171-3
[(1R,2S,4S,6S,8R,9R,11S)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 163052641 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)CO)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
[(1R,2S,4S,6S,9R,11S)-9-(hydroxymethyl)-4-methyl-14-methylidene-8,13-dioxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 162961869 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(=O)C(CC3C1C(=C)C(=O)O3)CO)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
[(1S,2R,4R,6R,8S,9R,11R)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 101593132 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)C)O)C 364.40 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/S0031-9422(00)94519-9
[(1S,2R,4R,6R,8S,9S,11R)-8,9-dihydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 101593131 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)(C)O)O)C 380.40 unknown https://doi.org/10.1016/0031-9422(82)83171-3
[(1S,2R,4S,6R,8R,9R,11R)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 163188828 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)C)O)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
[(1S,2R,4S,6R,8S,9S,11R)-8,9-dihydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] (Z)-2-methylbut-2-enoate 162851648 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)(C)O)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
[(3aS,4R,5E,7S,9E,11aS)-4-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-7-yl] acetate 162849535 Click to see CC1=CCC(C(=CC(C2C(C1)OC(=O)C2=C)O)C)OC(=O)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
[8-Hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] 2-methylbut-2-enoate 163052639 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)CO)O)C 380.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
https://doi.org/10.1016/0031-9422(82)83171-3
[9-(Hydroxymethyl)-4-methyl-14-methylidene-8,13-dioxo-5,12-dioxatricyclo[9.3.0.04,6]tetradecan-2-yl] 2-methylbut-2-enoate 162961867 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(=O)C(CC3C1C(=C)C(=O)O3)CO)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 98949 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(82)83171-3
Argophyllin A 5477865 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)(C)O)O)C 380.40 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/S0031-9422(00)83555-4
Argophyllin B 14219389 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(CC3C1C(=C)C(=O)O3)CO)O)C 380.40 unknown https://doi.org/10.1016/0305-1978(89)90094-X
https://doi.org/10.1016/0031-9422(82)83171-3
Argophyllone B 101923686 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(=O)C(CC3C1C(=C)C(=O)O3)CO)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)83555-4
Eupatolide 5281460 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(82)83171-3
> Lipids and lipid-like molecules / Saccharolipids
Methyl 4-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoate 78407186 Click to see CC(CC(=O)OC)C(=O)C1=C(C(=CC=C1)OC2C(C(C(C(O2)CO)O)O)O)O 400.40 unknown https://doi.org/10.1016/S0031-9422(00)94519-9
https://doi.org/10.1016/0305-1978(89)90094-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
2-Hydroxy-5,12,13-trimethyltetracyclo[11.1.1.01,10.04,9]pentadecane-5-carboxylic acid 162996741 Click to see CC1CC2C3CCCC(C3CC(C24CC1(C4)C)O)(C)C(=O)O 306.40 unknown https://doi.org/10.1016/0031-9422(82)83171-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
5-[(5-Hydroxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl)oxy]-6-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol 162920727 Click to see C1=COC(C2C1C(C3C2O3)O)OC4C(C(C(C(C4O)O)O)O)CO 346.33 unknown https://doi.org/10.1016/0031-9422(82)83171-3
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ayapin 3083597 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC(=O)O3 190.15 unknown https://doi.org/10.1016/S0031-9422(00)94505-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/0031-9422(82)83171-3

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