Details Top

Internal ID UUID643fd992a981e590167900
Scientific name Vicia amurensis
Authority Oett.
First published in Trudy Bot. Sada Imp. Yur'evsk. Univ.6: 143 (1906)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Vicia amurensis is primarily cultivated as a forage legume. The above‑ground biomass is harvested as hay or made into silage for ruminant feeding. In addition, the crop is used as a green manure, where the standing or cut plants are incorporated into the soil to enrich nitrogen pools. The whole plant can also be processed into protein‑rich meal for compound feed, especially for cattle, sheep and goats.

Properties relevant to use:
The species establishes symbiotic nodules with Rhizobium, allowing atmospheric nitrogen fixation of roughly 100–150 kg N ha⁻¹ in temperate soils. Its shoots contain 14–20 % crude protein on a dry‑matter basis and have relatively low neutral detergent fiber (NDF) content (≈35–45 %), contributing to high digestibility for livestock. The plant tolerates low temperatures, enabling growth in early spring and late autumn, which extends the grazing season. Seed protein exhibits a balanced amino‑acid profile, making the meal suitable as a protein supplement.

Standards and regulation:
Vicia amurensis is subject to general national feed and forage safety regulations. In China it complies with the Feed Safety Standard (GB 13078) for livestock feed, and in the European Union it falls under Regulation (EC) No 767/2009 on the placing on the market and use of feed. No specific industry standards are dedicated solely to this species.

Sustainability and sourcing:
Cultivation of Vicia amurensis contributes to sustainable cropping systems by providing a nitrogen‑fixing component that reduces the need for synthetic fertilizers. Its tolerance to cold soils allows integration into rotations with cereals, improving soil organic matter and breaking pest cycles. The species is grown on marginal lands in northern China and the Russian Far East, supporting smallholder livestock enterprises while enhancing environmental resilience.

Synonyms Top

Scientific name Authority First published in
Vicia vaniotii H.Lév. Repert. Spec. Nov. Regni Veg.7: 230 (1909)
Vicia japonica var. pratensis Kom. Fl. Manshur.2: 613 (1904)
Vicia japonica var. silvatica Kom. Fl. Manshur.2: 613 (1904)
Vicia ussuriensis Oett.
Vicia amurensis var. pratensis (Kom.) H.Hara J. Jap. Bot.16: 258 (1940)
Vicia pallida var. pratensis (Kom.) Nakai J. Coll. Sci. Imp. Univ. Tokyo31: 469 (1911)
Vicia japonica subsp. amurensis (Oett.) Kitam. Acta Phytotax. Geobot.20: 198 (1962)
Vicia amurensis var. pratensi (Kom.) H.Hara J. Jap. Bot. 16(5): 258 1940
Vicia amurensis var. silvatica (Kom.) H.Hara J. Jap. Bot.16: 258 (1940)
Vicia amurensis f. sanneensis Y.Q.Jiang & S.M.Fu Fl. Intramongolica, ed. 2, 3: 673 (1989)
Vicia amurensis f. alba H.Ohashi & Tateishi J. Jap. Bot.52: 106 (1977)
Vicia japonica sensu auct.
Vicia amurensis var. silvatica (Kom.) Hara

Common names Top

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Language Common/alternative name
Japanese ノハラクサフジ
Chinese 大巢菜
Chinese 西藏凹乳芹根
Chinese 黑龙江野豌豆
Chinese 圆叶草藤

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Chita

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186168
USDA Plants VIAM7
Tropicos 13042947
KEW urn:lsid:ipni.org:names:524516-1
The Plant List ild-32580
Open Tree Of Life 136993
Observations.org 123429
NCBI Taxonomy 154495
IPNI 524516-1
GBIF 2975174
EOL 643794
Elurikkus 8171
USDA GRIN 100256
CMAUP NPO4007

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
Identification of Vicia Species Native to South Korea Using Molecular and Morphological Characteristics Han S, Sebastin R, Wang X, Lee KJ, Cho GT, Hyun DY, Chung JW Front Plant Sci 09-Feb-2021
PMCID:PMC7900155
doi:10.3389/fpls.2021.608559
PMID:33633762
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
All that glitters is not Ramularia Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW Stud Mycol 29-Jun-2016
PMCID:PMC4986539
doi:10.1016/j.simyco.2016.06.001
PMID:27570325
Auxin biosynthesis and storage forms Korasick DA, Enders TA, Strader LC J Exp Bot 10-Apr-2013
PMCID:PMC3695655
doi:10.1093/jxb/ert080
PMID:23580748
Phylogenetic lineages in Pseudocercospora Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJ, Shin HD, Nakashima C, Groenewald JZ Stud Mycol 06-Jun-2012
PMCID:PMC3713886
doi:10.3114/sim0005
PMID:24014898
Phylogenetic lineages in the Capnodiales Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ Stud Mycol 01-Jan-2009
PMCID:PMC2816965
doi:10.3114/sim.2009.64.02
PMID:20169022
Two new acylated flavonol glycosides from Vicia amurensis. Kang SS, Chang YS, Kim JS Chem Pharm Bull (Tokyo) 01-Aug-2000
doi:10.1248/CPB.48.1242
PMID:10959600

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 acid esters
Methyl 3-phenylpropionate 7643 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 11868539 Click to see 324.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see 320.50 unknown via CMAUP database
Labdanediol 11130717 Click to see 310.50 unknown via CMAUP database
Labdanic Acid 11186394 Click to see 324.50 unknown via CMAUP database
Labdanic Acid Methyl Ester 7057547 Click to see 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledum camphor 92812 Click to see 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see 236.39 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[2-[[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73109610 Click to see 932.80 unknown https://doi.org/10.1248/CPB.48.1242
2-(3,4-Dihydroxyphenyl)-3-(4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-((3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl)oxan-2-yl)oxy-5,7-dihydroxychromen-4-one 14299117 Click to see 756.70 unknown https://doi.org/10.1248/CPB.48.1242
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 Click to see 626.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-((6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-4H-1-benzopyran-4-one 102148697 Click to see 610.50 unknown via CMAUP database
Alcesefoliside 11828754 Click to see 756.70 unknown https://doi.org/10.1248/CPB.48.1242
Amurenoside A 10653411 Click to see 932.80 unknown https://doi.org/10.1248/CPB.48.1242
Amurenoside B 11803929 Click to see 932.80 unknown https://doi.org/10.1248/CPB.48.1242
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Benzenepropanoic acid 107 Click to see 150.17 unknown via CMAUP database

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