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Alnus rubra

Alnus rubra - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Alnus rubra - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Alnus rubra - 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 UUID644039040fc89445942604
Scientific name Alnus rubra
Authority Bong.
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 2: 162 (1833)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alnus incana var. rubra (Bong.) Regel Nouv. Mém. Soc. Imp. Naturalistes Moscou 13(2): 157 1861
Alnus oregana Nutt. N. Amer. Sylv. 1: 9 (1842)
Alnus rubra var. pinnatisecta Starker J. Forest. (Washington) 37: 115 (1939)
Alnus rubra f. pinnatisecta (Starker) Rehder Bibl. Cult. Trees : 104 (1949)

Common names Top

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Language Common/alternative name
English red alder
English western alder
English oregon alder
Spanish aliso rojo
Spanish aliso rojo americano
Arabic نغت أحمر
Azerbaijani qırmızı qızılağac
azb قیرمیزی قیزیل آغاج
Bulgarian червена елша
Catalan aulne rouge
Welsh gwernen goch
German rot-erle
German roterle
German oregon-erle
German aulne rouge
Persian توسکای قرمز
Finnish oregoninleppä
Finnish punaleppä
French aulne rouge
Hebrew אלנוס מאדים
Hungarian vörös éger
Icelandic ryðölur
Italian ontano rosso
Japanese レッドオルダー
Japanese アメリカアカハンノキ
koi Гӧрд ловпу
Lithuanian aulne rouge
Norwegian Bokmål rødor
Polish olsza czerwona
Russian Ольха красная
Swedish rödal
Swedish aulne rouge
udm Горд лулпу
Chinese 赤楊
Chinese 美國赤楊
Chinese 红桤木

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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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
  • Northern America
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Subarctic America
      • Alaska
      • Yukon
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000947467
UNII SC957G7NBA
Canadensys 3679
USDA Plants ALRU2
Tropicos 3600058
INPN 610834
KEW urn:lsid:ipni.org:names:294986-1
The Plant List kew-6584
PaleoBotany 81345
Open Tree Of Life 639117
Observations.org 141823
NCBI Taxonomy 109069
NBN Atlas NBNSYS0000042064
Nature Serve 2.136265
IUCN Red List 194598
IPNI 294986-1
iNaturalist 56034
GBIF 2876176
Freebase /m/029k_4
FEIS plants/tree/alnrub
EPPO ALURB
EOL 1145612
Elurikkus 2689
Calflora (Californian flora) 253
US Library of Congress sh85112026
USDA GRIN 105118
Wikipedia Alnus_rubra
PFAF Alnus rubra

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_028654335.1 ASM2865433v1 Contig NCGR 2023-02-15 93.0x 525.25 Mb

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Succession and climatic stochasticity induce long-term decline of a forest browser Long ES, Tham EJ, Ferrer RP PLoS One 27-Feb-2024
PMCID:PMC10898743
doi:10.1371/journal.pone.0298231
PMID:38412173
High Frankia abundance and low diversity of microbial community are associated with nodulation specificity and stability of sea buckthorn root nodule Liu H, Ni B, Duan A, He C, Zhang J Front Plant Sci 21-Feb-2024
PMCID:PMC10915256
doi:10.3389/fpls.2024.1301447
PMID:38450407
Diversity of Wickerhamomyces (Wickerhamomycetaceae, Saccharomycetales) in China with the description of four new species Chai CY, Ke T, Niu QH, Hui FL Front Microbiol 08-Feb-2024
PMCID:PMC10881795
doi:10.3389/fmicb.2024.1338231
PMID:38389540
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Pest categorisation of Pestalotiopsis microspora Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 21-Dec-2023
PMCID:PMC10733803
doi:10.2903/j.efsa.2023.8493
PMID:38130321
Associations between shade tolerance and wood specific gravity for conifers in contrast to angiosperm trees: Foundations of the conifer fitness‐enhancing shade tolerance hypothesis Tucker GF, Maguire DA, Tupinambá‐Simões F Plant Environ Interact 13-Dec-2023
PMCID:PMC10840375
doi:10.1002/pei3.10131
PMID:38323133
Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses Bejerman N, Dietzgen R, Debat H Viruses 10-Dec-2023
PMCID:PMC10747219
doi:10.3390/v15122402
PMID:38140643
Quaternary palaeoecology meets deep-time palaeobiology Birks HJ Proc Natl Acad Sci U S A 01-Nov-2023
PMCID:PMC10655553
doi:10.1073/pnas.2316233120
PMID:37910534
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Mechanism of fungal remediation of wetland water: Stropharia rugosoannulata as promising fungal species for the development of biofilters to remove clinically important pathogenic and antibiotic resistant bacteria in contaminated water Sen K, Llewellyn M, Taheri B, Turner RJ, Berglund T, Maloney K Front Microbiol 18-Oct-2023
PMCID:PMC10642173
doi:10.3389/fmicb.2023.1234586
PMID:37965549
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900

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 / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.3109/13880209509088144
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aS,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162952656 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/JPS.2600620129
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163185435 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600620129
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.3109/13880209509088144
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600620129
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/JPS.2600620129
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3109/13880209509088144
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880209509088144
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880209509088144
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(3R)-1,7-bis(3,4-dihydroxyphenyl)heptan-3-yl]oxy-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 54585388 Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 626.60 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
(E)-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)hept-4-en-3-one 11570978 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O 312.40 unknown https://doi.org/10.1055/S-2006-957372
[(2R,3S,4S,5R,6R)-6-[(3S)-1,7-bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 10746324 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O 612.60 unknown https://doi.org/10.1055/S-2006-957372
https://doi.org/10.1021/NP980083L
[6-[1,7-Bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 85253869 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O 612.60 unknown https://doi.org/10.1055/S-2006-957372
1-(3,4-Dihydroxyphenyl)-7-(4-hydroxyphenyl)hept-4-en-3-one 73015010 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O 312.40 unknown https://doi.org/10.1055/S-2006-957372
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 14707657 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.1055/S-2006-957372
1,7-Bis(4-hydroxyphenyl)-4-hepten-3-one 53840022 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1055/S-2006-957372
CID 45783118 45783118 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 508.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Hirsutal 13347317 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1055/S-2006-957372
Hirsutanonol 9928190 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1055/S-2006-957372
https://doi.org/10.1021/NP980083L
Hirsutanonol 5-O-glucoside 14707659 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 508.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Oregonin 14707658 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.3109/13880209509088144
https://doi.org/10.1021/NP980083L
https://doi.org/10.1055/S-2006-957372
Platyphyllenone 23786382 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1055/S-2006-957372
Rubranoside A 10097263 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Rubranoside B 24011643 Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O 464.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Rubranoside D 10532003 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCCCC3=CC(=C(C=C3)O)O)CCC4=CC(=C(C=C4)O)O)O)O)O)O)(CO)O 626.60 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5S)-1,7-bis(4-hydroxyphenyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptan-3-one 10599483 Click to see C1C(C(C(C(O1)OC(CCC2=CC=C(C=C2)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O 446.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
1,7-Bis(4-hydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 74203441 Click to see C1C(C(C(C(O1)OC(CCC2=CC=C(C=C2)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O 446.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
1,7-Bis(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one 14833391 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Platyphylloside 9826264 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6R)-6-[(3S)-1,7-bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 10699511 Click to see COC1=C(C=CC(=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O)O 658.60 unknown https://doi.org/10.1021/NP980083L
https://doi.org/10.1055/S-2006-957372
[6-[1,7-Bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 85237419 Click to see COC1=C(C=CC(=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O)O 658.60 unknown https://doi.org/10.1055/S-2006-957372

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