Adiantum pedatum - Unknown
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Internal ID UUID64407715f1736002774886
Scientific name Adiantum pedatum
Authority L.
First published in Sp. Pl. 2: 1095. 1753 [1 May 1753]

Description Top

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Synonyms Top

Scientific name Authority First published in
Adiantum americanum Nieuwl. Amer. Midl. Naturalist 2: 280 (1912)
Adiantum boreale C.Presl Tent. Pterid. : 158 (1836)
Adiantum pedatum f. billingsae Kittr. Amer. Fern J. 19: 56 (1929)
Adiantum pedatum f. laciniatum (Hopkins) Weath. Amer. Fern J. 27: 52 (1937)
Adiantum pedatum var. kamtschaticum Rupr. Dist. Crypt. Vasc. Ross. 48. 1845 [Jul 1845] ; alt. title: Beitr. Pflanzenk. Russ. Reiches 3: 49. Jul 1845
Adiantum pedatum f. triangulare (McCord) M.Broun Index No. Amer. Ferns 16. 1938
Adiantum pedatum f. contratum Yonek. & Keizo Sasaki J. Jap. Bot. 89(5): 361. 2014 [20 Oct 2014]
Adiantum pedatum var. laciniatum Hopkins Ohio Naturalist 10: 180, fig. 1. 1910
Adiantum pedatum var. originarium Wherry Amer. Fern J. 27: 58. 1937
Adiantum pedatum var. praeflexum Copel. ex C.F.Baker West Amer. Pl. 2: 7. 1903 , nomen
Adiantum pedatum var. rangiferinum E.S.Burgess Proc. & Trans. Roy. Soc. Canada 4, Sect. 4: 11. 1886
Adiantum pedatum var. triangulare McCord Canad. Naturalist Geol. n.s., 1(no. 5): 355. 1864 [Oct 1864]
Adiantum pedatum var. tripartitum Farw. Amer. Fern J. 27: 12. 1937

Common names Top

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Language Common/alternative name
English northern maidenhair
English northern maidenhair fern
Azerbaijani qədəhvari adiant
Azerbaijani qədəhvari baldırıqara
German pfauenrad-frauenhaarfarn
German hufeisenfarn
German pfauenradfarn
Persian سرخس گیسوی شمالی
French adiante pédalée
French capillaire du canada
French adiante du canada
Japanese クジャクシダ
Korean 공작초
Korean 공작고사리
Dutch hoefijzervaren
Russian Адиантум стоповидный
Swedish frilandsadiantum
Chinese 铁扇子
Chinese 北方鐵線蕨
Chinese 北方铁线蕨
Chinese 铁丝七
Chinese 掌叶铁线蕨

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Adiantum pedatum var. grandifolium (Ching) Ching Acta Phytotax. Sin. 6(4): 324 1957

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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.
pour boiling water over milled sphagnum moss, sow seeds, enclose in plastic bag

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001107191
UNII XI62A0JDC5
Flora of Alabama 167
Canadensys 8382
USDA Plants ADPE
Tropicos 26600011
KEW urn:lsid:ipni.org:names:30004419-2
The Plant List tro-26600011
Plantarium 738
Missouri Botanical Garden 285642
PaleoBotany 117652
Open Tree Of Life 190952
Observations.org 137984
NCBI Taxonomy 29590
NBN Atlas NBNSYS0200001661
Nature Serve 2.135425
IPNI 17012140-1
iNaturalist 48435
GBIF 2651832
Freebase /m/05zzd6z
WisFlora 8511
EPPO ADIPE
EOL 597685
Elurikkus 2553
USDA GRIN 401921
Wikipedia Adiantum_pedatum
PFAF Adiantum pedatum

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
Effects of nitrogen addition on species composition and diversity of early spring herbs in a Korean pine plantation Yang G, Zhang M, Jin G Ecol Evol 05-Sep-2023
PMCID:PMC10480043
doi:10.1002/ece3.10498
PMID:37674646
The Antiproliferative Activity of Adiantum pedatum Extract and/or Piceatannol in Phenylhydrazine-Induced Colon Cancer in Male Albino Rats: The miR-145 Expression of the PI-3K/Akt/p53 and Oct4/Sox2/Nanog Pathways Khamis T, Diab AA, Zahra MH, El-Dahmy SE, Abd Al-Hameed BA, Abdelkhalek A, Said MA, Abdellatif H, Fericean LM, Banatean-Dunea I, Arisha AH, Attia MS Molecules 20-Jul-2023
PMCID:PMC10383735
doi:10.3390/molecules28145543
PMID:37513415
Assessing the effect of roads on mountain plant diversity beyond species richness Li H, Luo P, Yang H, Luo C, Xie W, Jia H, Cheng Y, Huang Y Front Plant Sci 26-Sep-2022
PMCID:PMC9549253
doi:10.3389/fpls.2022.985673
PMID:36226279
Exploiting Unreduced Gametes for Improving Ornamental Plants Xie L, Ke LZ, Lu XQ, Chen J, Zhang ZS Front Plant Sci 06-Jun-2022
PMCID:PMC9207335
doi:10.3389/fpls.2022.883470
PMID:35734261
Photographic analysis of field‐monitored fern gametophyte development and response to environmental stress Schneller JJ, Farrar DR Appl Plant Sci 11-Apr-2022
PMCID:PMC9039794
doi:10.1002/aps3.11470
PMID:35495189
Effects of Rhododendron removal and prescribed fire on bees and plants in the southern Appalachians Ulyshen M, Elliott K, Scott J, Horn S, Clinton P, Liu N, Miniat CF, Caldwell P, Oishi C, Knoepp J, Bolstad P Ecol Evol 01-Mar-2022
PMCID:PMC8888263
doi:10.1002/ece3.8677
PMID:35261754
Comparison of Herbal Medicines Used for Women’s Menstruation Diseases in Different Areas of the World Jiao M, Liu X, Ren Y, Wang Y, Cheng L, Liang Y, Li Y, Zhang T, Wang W, Mei Z Front Pharmacol 04-Feb-2022
PMCID:PMC8854496
doi:10.3389/fphar.2021.751207
PMID:35185533
Inferring the impacts of evolutionary history and ecological constraints on spore size and shape in the ferns Barrington DS, Patel NR, Southgate MW Appl Plant Sci 20-Apr-2020
PMCID:PMC7186895
doi:10.1002/aps3.11339
PMID:32351800
An update and reassessment of fern and lycophyte diversity data in the Japanese Archipelago Ebihara A, Nitta JH J Plant Res 16-Sep-2019
PMCID:PMC6831535
doi:10.1007/s10265-019-01137-3
PMID:31529289
Soil chemistry, and not short-term (1–2 year) deer exclusion, explains understory plant occupancy in forests affected by acid deposition Begley-Miller DR, Diefenbach DR, McDill ME, Drohan PJ, Rosenberry CS, Just Domoto EH AoB Plants 09-Aug-2019
PMCID:PMC6799995
doi:10.1093/aobpla/plz044
PMID:31649810
Identification and Evaluations of Novel Insecticidal Proteins from Plants of the Class Polypodiopsida for Crop Protection against Key Lepidopteran Pests Liu L, Schepers E, Lum A, Rice J, Yalpani N, Gerber R, Jiménez-Juárez N, Haile F, Pascual A, Barry J, Qi X, Kassa A, Heckert MJ, Xie W, Ding C, Oral J, Nguyen M, Le J, Procyk L, Diehn SH, Crane VC, Damude H, Pilcher C, Booth R, Liu L, Zhu G, Nowatzki TM, Nelson ME, Lu AL, Wu G Toxins (Basel) 01-Jul-2019
PMCID:PMC6669613
doi:10.3390/toxins11070383
PMID:31266212
A novel approach for the metric analysis of fern fronds: Growth and architecture of the Mesozoic fern Weichselia reticulata in the light of modern ferns Blanco-Moreno C, Gomez B, Marugán-Lobón J, Daviero-Gomez V, Buscalioni ÁD PLoS One 27-Jun-2019
PMCID:PMC6597107
doi:10.1371/journal.pone.0219192
PMID:31247026
A review of the use of pteridophytes for treating human ailments Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB J Zhejiang Univ Sci B 01-Feb-2018
PMCID:PMC5833325
doi:10.1631/jzus.B1600344
PMID:29405039
Convergent Evolution of Fern-Specific Mitochondrial Group II Intron atp1i361g2 and Its Ancient Source Paralogue rps3i249g2 and Independent Losses of Intron and RNA Editing among Pteridaceae Zumkeller SM, Knoop V, Knie N Genome Biol Evol 04-Aug-2016
PMCID:PMC5010907
doi:10.1093/gbe/evw173
PMID:27492234
Morphological Examination and Phylogenetic Analyses of Phycopeltis spp. (Trentepohliales, Ulvophyceae) from Tropical China Zhu H, Zhao Z, Xia S, Hu Z, Liu G PLoS One 02-Feb-2015
PMCID:PMC4314078
doi:10.1371/journal.pone.0114936
PMID:25643363

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 / Diterpenoids / Colensane and clerodane diterpenoids
3a,5a,7a,11b,13a-Pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene-8-carboxylic acid 73082660 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC=C5C(=O)O)C)C)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.41.268
Filic-3-ene 12309889 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Diplopterol 164874 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3a,5a,8,11a,13a-Pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-8-yl)methanol 12309133 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)CO)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.41.268
(3R,3aR,5aR,5bR,7aS,11aS,11bR,13aS,13bR)-3a,5a,7a,11b,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene-8-carboxylic acid 162981694 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC=C5C(=O)O)C)C)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.41.268
(3R,3aR,5aR,5bS,7aS,11aS,11bR,13aS,13bR)-3a,5a,7a,11b,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene-8-carbaldehyde 101596938 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC=C5C=O)C)C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.41.268
https://doi.org/10.1016/S0040-4039(01)84172-1
(3R,3aR,5aS,7aS,11aS,11bR,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857703 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.41.268
(3R,3aR,5aS,7aS,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene 13857712 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3=CCC5C4(CCCC5(C)C)C)C)C)C 408.70 unknown https://doi.org/10.1039/C19680001105
[(3R,3aR,5aR,5bR,7aR,8R,11aS,13aS,13bR)-3a,5a,8,11a,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-8-yl]methanol 101170706 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)CO)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.41.268
[(3R,3aR,5aR,5bS,7aR,8R,11aS,13aS,13bR)-3a,5a,8,11a,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysen-8-yl]methanol 162882351 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)CO)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.41.268
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857699 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4039(01)84172-1
Fern-8-ene 12311006 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4=C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.41.268
Fernene 441679 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4039(01)84172-1
https://doi.org/10.1248/CPB.41.268
Filicene 12309888 Click to see CC1=CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CCC5C(C)C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0040-4039(01)84172-1
Neohop-12-ene 13857697 Click to see CC(C)C1CCC2C1(CCC3(C2=CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.41.268
Tetrahymanol 168951 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3R,3aR,5aS,5bR,7aS,11aS,11bR)-3a,5a,5b,8,8,11a-hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b-dodecahydrocyclopenta[a]chrysene 12444932 Click to see CC(C)C1CCC2=C3C=CC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 408.70 unknown https://doi.org/10.1039/C19680001105
Hopene II 12310619 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-one 14605584 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5=O)C)C)C)C)C 384.60 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-(3-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl)ethanone 73746297 Click to see CC(=O)C1(CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.41.268
1-[(3R,3aR,5aR,5bR,7aS,11aS,11bR,13aR,13bR)-3-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl]ethanone 21159071 Click to see CC(=O)C1(CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.41.268
1-[(3R,3aR,5aR,5bR,7aS,11aS,11bR,13aS,13bR)-3-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-2,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-3-yl]ethanone 162897135 Click to see CC(=O)C1(CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1248/CPB.41.268
Adiantone 15558363 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1248/CPB.41.268
https://doi.org/10.1016/S0040-4039(01)84172-1
Isoadiantone 3041569 Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 412.70 unknown https://doi.org/10.1248/CPB.41.268
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl) acetate 85115783 Click to see CC(=O)OC1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
[(1S)-1-[(3R,3aS,5aR,5bR,7aS,11aS,11bR,13aS,13bS)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]ethyl] acetate 162915056 Click to see CC(C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)OC(=O)C 456.70 unknown https://doi.org/10.1248/CPB.41.268
[(3S,3aR,5aR,5bR,7aS,11aS,11bR,13aR,13bR)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl] acetate 15819211 Click to see CC(=O)OC1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
1-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)ethyl acetate 14656418 Click to see CC(C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)OC(=O)C 456.70 unknown https://doi.org/10.1248/CPB.41.268
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(4S,4aR,6aR,6aR,6bR,8aR,12aS,14aR,14bR)-4-hydroxy-4,6a,6b,9,9,12a,14b-heptamethyl-2,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydro-1H-picen-3-one 163100029 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
(4S,4aR,6aR,6aR,6bR,8aS,12aS,14aR,14bR)-4-hydroxy-4,6a,6b,9,9,12a,14b-heptamethyl-2,4a,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydro-1H-picen-3-one 101280264 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
Ketohakonanol 90720428 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
> Organoheterocyclic compounds / Naphthopyrans
(6S,14R,18S)-6,10,10,14,15,20-hexamethyl-21-oxahexacyclo[17.3.2.01,18.02,15.05,14.06,11]tetracosan-20-ol 5316485 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C46CCC5C(OC6)(C)O)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
Adipedatol 12127456 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C46CCC5C(OC6)(C)O)C)C)C)C 428.70 unknown https://doi.org/10.1248/CPB.41.268
https://doi.org/10.1016/S0040-4039(01)84172-1

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