Scientific name	Authority	First published in
Crinum erubescens var. brasiliense	Herb.	Amaryllidaceae : 251 (1837)
Crinum erubescens var. caraccense	Herb.	Amaryllidaceae : 252 (1837)
Crinum erubescens var. corantinum	Herb.	Amaryllidaceae : 251 (1837)
Crinum erubescens var. majus	Herb.	Amaryllidaceae 251. 1837
Crinum erubescens var. minus	Herb.	Amaryllidaceae 251. 1837
Crinum erubescens var. octoflorum	Herb.	Amaryllidaceae : 252 (1837)
Crinum erubescens var. rubrilimbum	Herb.	Appendix : 21 (1821)
Amaryllis procera	Salisb.	Prodr. Stirp. Chap. Allerton : 230 (1796)
Crinum attenuatum	Willd. ex Schult.f.	Syst. Veg., ed. 15 bis 7: 873 (1830)
Crinum commelinianum	Herb.	Amaryllidaceae : 254 (1837)
Crinum commelyni	Jacq.	Pl. Hort. Schoenbr. 2: 40 (1797)
Crinum corantinum	Herb. ex Steud.	Nomencl. Bot. , ed. 2, 1: 439 (1840)
Crinum corantynum	M.Roem.	Fam. Nat. Syn. Monogr. 4: 80 (1847)
Crinum crucibulum	D.Dietr.	Syn. Pl. 2: 1181 (1840)
Crinum cruentum	[Ker-Gawl.]	Bot. Reg. 2: t. 171 (1817)
Crinum dieterichii	Schult.	Observ. Bot. : 65 (1809)
Crinum gordonianum	M.Roem.	Fam. Nat. Syn. Monogr. 4: 80 (1847)
Crinum guianense	M.Roem.	Fam. Nat. Syn. Monogr. 4: 80 (1847)
Crinum inodorum	Tausch	Flora 19(2): 422 (1836)
Crinum lanceanum	Willd. ex M.Roem.	Fam. Nat. Syn. Monogr. 4: 94 (1847)
Crinum lancei	Herb. ex Sweet	Hort. Brit. , ed. 3: 677 (1839)
Crinum lindleyanum	Herb.	Amaryllidaceae : 252 (1837)
Crinum lindleyanum	Schult.f. ex Seub.	Fl. Bras. 3(1): 159 (1847)
Crinum loddigesianum	Herb.	Amaryllidaceae : 253 (1837)
Crinum octoflorum	Herb. ex Steud.	Nomencl. Bot. , ed. 2, 1: 440 (1840)
Crinum odoratissimum	Tausch	Flora 19: 422 (1886)
Crinum rubrilimbum	Sweet ex Steud.	Nomencl. Bot. , ed. 2, 1: 440 (1840)
Crinum viridifolium	M.Roem.	Fam. Nat. Syn. Monogr. 4: 78 (1847)
Crinum erubescens var. mexicanum	M.Roem.	Fam. Nat. Syn. Monogr. 4: 79. 1847
Crinum cruentum var. albidum	Kunth	Enum. Pl. 5: 555. 1850
Crinum pumilum	Salisb.	Gen. Pl. : 115 (1866)
Crinum soboliferum	Salisb.	Gen. Pl. : 115 (1866)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Swedish	sydlig sumpkrinum

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- Mexico
  - Mexico Central
  - Mexico Southwest

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Trinidad-Tobago
- Central America
  - Belize
  - Costa Rica
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Paraguay
- Western South America
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000764495
Tropicos	1200698
INPN	446776
KEW	urn:lsid:ipni.org:names:30032850-2
The Plant List	kew-303415
Open Tree Of Life	118208
NCBI Taxonomy	209093
IPNI	30032850-2
iNaturalist	283431
GBIF	2853616
EOL	1087175
USDA GRIN	12223
CMAUP	NPO16454

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

Population size as a major determinant of mating system and population genetic differentiation in a narrow endemic chasmophyte

Surina B, Balant M, Glasnović P, Radosavljević I, Fišer Ž, Fujs N, Castro S

BMC Plant Biol

09-Aug-2023

PMCID:	PMC10411015
doi:	10.1186/s12870-023-04384-8
PMID:	37553615

Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin

Evidente A

Molecules

12-May-2023

PMCID:	PMC10224442
doi:	10.3390/molecules28104055
PMID:	37241796

Cripowellins Pause Plasmodium falciparum Intraerythrocytic Development at the Ring Stage

Butler JH, Painter HJ, Bremers EK, Krai P, Llinás M, Cassera MB

Molecules

13-Mar-2023

PMCID:	PMC10056369
doi:	10.3390/molecules28062600
PMID:	36985570

Amaryllidaceae plants: a potential natural resource for the treatment of Chagas disease

Martínez-Peinado N, Cortes-Serra N, Tallini LR, Pinazo MJ, Gascon J, Bastida J, Alonso-Padilla J

Parasit Vectors

26-Jun-2021

PMCID:	PMC8235838
doi:	10.1186/s13071-021-04837-9
PMID:	34174959

Biosynthesis and Biological Activities of Newly Discovered Amaryllidaceae Alkaloids

Ka S, Koirala M, Mérindol N, Desgagné-Penix I

Molecules

23-Oct-2020

PMCID:	PMC7660210
doi:	10.3390/molecules25214901
PMID:	33113950

Alkaloids from Plants with Antimalarial Activity: A Review of Recent Studies

Uzor PF

Evid Based Complement Alternat Med

12-Feb-2020

PMCID:	PMC7037883
doi:	10.1155/2020/8749083
PMID:	32104196

Antiplasmodial natural products: an update

Tajuddeen N, Van Heerden FR

Malar J

05-Dec-2019

PMCID:	PMC6896759
doi:	10.1186/s12936-019-3026-1
PMID:	31805944

The dark side of the black caiman: Shedding light on species dietary ecology and movement in Agami Pond, French Guiana

Caut S, Francois V, Bacques M, Guiral D, Lemaire J, Lepoint G, Marquis O, Sturaro N

PLoS One

24-Jun-2019

PMCID:	PMC6590786
doi:	10.1371/journal.pone.0217239
PMID:	31233530

Isolation, structure elucidation, and synthesis of antiplasmodial quinolones from Crinum firmifolium

Presley CC, Du Y, Dalal S, Merino EF, Butler JH, Rakotonandrasana S, Rasamison VE, Cassera MB, Kingston DG

Bioorg Med Chem

13-Jun-2017

PMCID:	PMC5557408
doi:	10.1016/j.bmc.2017.06.017
PMID:	28648491

New potently bioactive alkaloids from Crinum erubescens

Presley CC, Krai P, Dalal S, Su Q, Cassera M, Goetz M, Kingston DG

Bioorg Med Chem

30-Aug-2016

PMCID:	PMC5065785
doi:	10.1016/j.bmc.2016.08.058
PMID:	27624525

Shade treatment affects structure and recovery of invasive C4 African grass Echinochloa pyramidalis

López Rosas H, Moreno-Casasola P, Espejel González VE

Ecol Evol

01-Mar-2015

PMCID:	PMC4377275
doi:	10.1002/ece3.1434
PMID:	25859337

Phytochemical Profile Top

Add a new one!

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see CC(CC(=O)NC(=O)C1=COC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	435.50	unknown	via CMAUP database
Himeic acid B	21579676	Click to see C1=C(OC=C(C1=O)C(=O)N)C=CCCCCCCCCC(=O)O	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see CC(CC(=O)NC(=O)C1=CNC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic acid propylamide	10379895	Click to see CCCCCCCCCCCCCCCC(=O)NCCC	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see CC1CC(=O)CC(C1(CC(=O)C(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C)O)(C)C	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see CCCCCC(=O)OCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(=O)CC1(C)C)C)O)C)C#CC2=C(CC(CC2(C)C)O)C	713.00	unknown	via CMAUP database
Amarouciaxanthin B/Sidnyaxanthin	16061221	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC2(C(=CC(=O)CC2(C)C)C)O)C)C	596.80	unknown	via CMAUP database
CID 23428237	23428237	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C=C2C(=CC(=O)CC2(C)C)C)C)C	578.80	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC23C(CC(CC2(O3)C)O)(C)C)C)C	598.90	unknown	via CMAUP database
Mytiloxanthin	11365423	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C	598.90	unknown	via CMAUP database
NV766Twa77	102146782	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol	439423	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see C[N+](C)(C)CC(=O)O	118.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Arginine	6322	Click to see C(CC(C(=O)O)N)CN=C(N)N	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)CC2=C(C=CC(=C2)CC(C(=O)O)N)O)O	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see C(CS(=O)(=O)O)N	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see CC1CCC2C(C1)C=CC(C2(C)C(=O)CCO)(C)O	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5C(=O)N4)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3=O)C(C5CC67CCCN6C(=O)C5(C(O4)O)NC7=O)(C)C)C	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5(C(=O)N4)OC)C(C)(C)C=C)C	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5(N4C(=O)C6CCCN6C5=O)O)O)C(C)(C)C=C)C	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)C	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)O)C	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(=O)C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	445.50	unknown	via CMAUP database
notoamide R	46919488	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)(O)O	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)O	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)(O)O	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Crinum erubescens

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top