Castanea dentata - Unknown
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Details Top

Internal ID UUID64402a7c04151864546448
Scientific name Castanea dentata
Authority Borkh.
First published in Theor. Prakt. Handb. Forstbot. 1: 741 (1800)

Description Top

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Synonyms Top

Scientific name Authority First published in
Castanea vesca var. denuda Alph.Wood Class-book Bot. : 832 (1881)
Castanea americana Raf. Fl. Ludov. : 134 (1817)
Castanea sativa var. americana (Michx.) Sarg. Gard. & Forest 2: 484 (1889)
Castanea sativa var. pendulifolia Lavallée Énum. Arbres 113. 1885
Castanea vesca var. americana Michx. Fl. Bor.-Amer. 2: 193 (1803)
Castanea vulgaris var. americana (Michx.) A.DC. Prodr. 16(2): 114 (1864)
Fagus castanea var. dentata Marshall Arbust. Amer. 46. 1785
Fagus dentata Marshall Arbust. Amer. 46–47 1785

Common names Top

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Language Common/alternative name
English american chestnut
ang Ƿīnlandisc ceastanhnutu
ang Ƿīnlendisc ceastanhnutu
ang Ƿīnlendisc cystel
Bulgarian американски кестен
Catalan castanyer americà
Cherokee ᎤᎾᎩᎾ
German amerikanische kastanie
Persian شاهبلوط آمریکایی
Finnish amerikankastanja
French châtaignier d'amérique
French châtaignier américain
Galician castiñeiro americano
Hebrew ערמון אמריקאי
Croatian obični američki kesten
Hungarian amerikai gesztenye
Japanese アメリカグリ
Korean 미국밤나무
Latvian zobainā kastaņa
Norwegian Bokmål amerikakastanje
Polish kasztan amerykański
Polish kasztan zębaty
Russian Каштан американский
Russian Каштан зубчатый
Russian каштан американский
Chinese 美洲栗

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Delaware
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000811441
UNII 7574YJE22M
Florida Plant Atlas 937
Flora of Alabama 2143
Canadensys 5956
USDA Plants CADE12
Tropicos 13100209
KEW urn:lsid:ipni.org:names:295320-1
The Plant List kew-34965
Missouri Botanical Garden 280744
Open Tree Of Life 562865
NCBI Taxonomy 134033
Nature Serve 2.153295
IUCN Red List 62004455
IPNI 295320-1
iNaturalist 49186
GBIF 5333230
Freebase /m/0hsj0
WisFlora 3046
EPPO CSNDE
EOL 1148514
Calflora (Californian flora) 12338
USDA GRIN 9435
Wikipedia American_chestnut
CMAUP NPO9606

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
Genomic prediction of resistance to Hymenoscyphus fraxineus in common ash (Fraxinus excelsior L.) populations Meger J, Ulaszewski B, Pałucka M, Kozioł C, Burczyk J Evol Appl 03-May-2024
PMCID:PMC11069026
doi:10.1111/eva.13694
PMID:38707993
Clinging to the top: natal dispersal tracks climate gradient in a trailing-edge population of a migratory songbird Gaya HE, Cooper RJ, Delancey CD, Hepinstall-Cymerman J, Kurimo-Beechuk EA, Lewis WB, Merker SA, Chandler RB Mov Ecol 16-Apr-2024
PMCID:PMC11020467
doi:10.1186/s40462-024-00470-0
PMID:38627871
Scaling approaches and macroecology provide a foundation for assessing ecological resilience in the Anthropocene Enquist BJ, Erwin D, Savage V, Marquet PA Philos Trans R Soc Lond B Biol Sci 08-Apr-2024
PMCID:PMC10999275
doi:10.1098/rstb.2023.0010
PMID:38583479
Mapping QTLs for blight resistance and morpho-phenological traits in inter-species hybrid families of chestnut (Castanea spp.) Fan S, Georgi LL, Hebard FV, Zhebentyayeva T, Yu J, Sisco PH, Fitzsimmons SF, Staton ME, Abbott AG, Nelson CD Front Plant Sci 08-Apr-2024
PMCID:PMC11033410
doi:10.3389/fpls.2024.1365951
PMID:38650705
Interconnecting global threats: climate change, biodiversity loss, and infectious diseases Pfenning-Butterworth A, Buckley LB, Drake JM, Farner JE, Farrell MJ, Gehman AL, Mordecai EA, Stephens PR, Gittleman JL, Davies TJ Lancet Planet Health 01-Apr-2024
PMCID:PMC11090248
doi:10.1016/S2542-5196(24)00021-4
PMID:38580428
Conservation Mitonuclear Replacement: Facilitated mitochondrial adaptation for a changing world Iverson EN Evol Appl 10-Mar-2024
PMCID:PMC10925831
doi:10.1111/eva.13642
PMID:38468713
Forecasting of Airborne Conidia Quantities and Potential Insect Associations of Cryphonectria parasitica, the Causal Agent of Chestnut Blight, in England Romon-Ochoa P, Samal P, Pace T, Newman T, Oram M, Baxter N, Manning JA, Biddle M, Barnard K, Inward D, Taylor P, Hendry S, Pérez-Sierra A, Ward L J Fungi (Basel) 28-Feb-2024
PMCID:PMC10971521
doi:10.3390/jof10030181
PMID:38535190
Advancing tree genomics to future proof next generation orchard production Kerr SC, Shehnaz S, Paudel L, Manivannan MS, Shaw LM, Johnson A, Velasquez JT, Tanurdžić M, Cazzonelli CI, Varkonyi-Gasic E, Prentis PJ Front Plant Sci 19-Jan-2024
PMCID:PMC10834703
doi:10.3389/fpls.2023.1321555
PMID:38312357
Cyto-molecular characterization of rDNA and chromatin composition in the NOR-associated satellite in Chestnut (Castanea spp.) Islam-Faridi N, Hodnett GL, Zhebentyayeva T, Georgi LL, Sisco PH, Hebard FV, Nelson CD Sci Rep 15-Jan-2024
PMCID:PMC10789788
doi:10.1038/s41598-023-45879-6
PMID:38225361
Spanish ecological battleground: population structure of two invasive fungi, Cryphonectria parasitica and Fusarium circinatum Ahmad F, Diez JJ Front Plant Sci 21-Dec-2023
PMCID:PMC10771289
doi:10.3389/fpls.2023.1310254
PMID:38186600
Constructing the public in public perceptions research: A case study of forest genomics Berseth V, Taylor J, Hutchen J, Nguyen V, Schott S, Klenk N Public Underst Sci 14-Dec-2023
PMCID:PMC11056085
doi:10.1177/09636625231210453
PMID:38095191
Tolerance evaluation and genetic relationship analysis among some economically important chestnut cultivars in Türkiye using drought-associated SSR and EST-SSR markers Kara D, Orhan E Sci Rep 28-Nov-2023
PMCID:PMC10684537
doi:10.1038/s41598-023-47951-7
PMID:38016998
Data analysis of polygalacturonase inhibiting proteins (PGIPs) from agriculturally important proteomes Acharya S, Troell HA, Billingsley RL, Lawrence KS, McKirgan DS, Alkharouf NW, Klink VP Data Brief 19-Nov-2023
PMCID:PMC10698527
doi:10.1016/j.dib.2023.109831
PMID:38076472
Going Asexual: A Survey of Mites of the Genus Thyreophagus (Acari: Acaridae) Revealing a Large Number of New Parthenogenetic Species in the Holarctic Region Klimov PB, Kolesnikov VB, Demard EP, Stinson CS, Merckx J, Duarte MV, Pedroso LG, Khaustov AA, Myers-Hansen JL, Wäkers FL, Vangansbeke D Life (Basel) 05-Nov-2023
PMCID:PMC10672012
doi:10.3390/life13112168
PMID:38004308
Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA Nutrients 31-Oct-2023
PMCID:PMC10647252
doi:10.3390/nu15214630
PMID:37960283

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilaurin 10851 Click to see CCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC 639.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(Z)-alpha-ocimene 5463455 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Parkeol 12313974 Click to see CC(CCC=C(C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 44423569 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(=C)C 454.80 unknown via CMAUP database
Cycloneolitsol 101306728 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 454.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24S)-24-Methyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630502 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
24,24-Dimethyllanosta-9(11),25-dien-3beta-ol 102504569 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 454.80 unknown via CMAUP database
4alpha,14alpha-Dimethyl-24-methylene-cholest-9(11)-en-3beta-ol 5283648 Click to see CC1C2CCC3C(=CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C)C2(CCC1O)C 426.70 unknown via CMAUP database
Agrostophyllinol 489917 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24S)-24-Ethyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630504 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C)C(=C)C 454.80 unknown via CMAUP database
(3S,4S,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-4,10,13,14-tetramethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 101630496 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(C)C 442.80 unknown via CMAUP database
(3S,4S,5S,8S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-4,10,13,14-tetramethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 101630497 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(=C)C 440.70 unknown via CMAUP database
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5H-7,4-Methenofuro(3,2-c)oxireno(f)oxacycloundecin-5-one,1a,2,3,7,11,11a-hexahydro-8,11a-dimethyl-, (1aS,7R,11aS)- 497202 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Linderalactone 6450191 Click to see CC1=CCCC2=CC(C3=C(C1)OC=C3C)OC2=O 244.28 unknown via CMAUP database
Pseudoneolinderane 57400551 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Zeylanin 12445041 Click to see CC1=CC2=C(C3C=C(CCC1OC(=O)C)C(=O)O3)C(=CO2)C 302.32 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
2H-10,1a-(Epoxymethano)oxireno(4,5)cyclodeca(1,2-b)furan-12-one, 3,6,10,10a-tetrahydro-5,9-methyl-, (1aS-(1aR*,4E,10R*,10aR*))- 6450227 Click to see CC1=CCCC23C(O2)C(C4=C(C1)OC=C4C)OC3=O 260.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-rhamnoside-7-O-glucoside 90795788 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O 594.50 unknown via CMAUP database

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