Eucalyptus cladocalyx, commonly known as sugar gum, is a species of eucalypt tree found in the Australian state of South Australia. It is found naturally in three distinct populations - in the Flinders Ranges, Eyre Peninsula and on Kangaroo Island. It is notable for its mottled colourful yellow to orange bark, strongly discolourous leaves and inflorescences grouped on leafless branchlets inside the tree crown. It is commonly cultivated as farm windbreaks and for timber, and is also known to be a suitable breeding habitat for the Yellow-tailed Black-Cockatoo. It is a fast-growing tree, efficient user of water, drought and frost tolerant, and has the capacity to spread up to 70 metres away from locations where it has been planted. The wood is termite resistant, with moderate strength and durability, and can be used for furniture, flooring, posts, construction timber and railway sleepers. It has become an invasive species in South Africa, where it is now registered as a category 2 invader plant.

Synonyms Top

Scientific name	Authority	First published in
Eucalyptus corynocalyx	F.Muell.	Fragm. 2: 43 (1860)
Eucalyptus langii	Maiden & Blakely	Crit. Revis. Eucalyptus 8: 72 (1929)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sugargum
English	sugar gum
Afrikaans	suikerbloekom
Esperanto	sukereŭkalipto
Persian	انگم شکری
Chinese	棒萼桉
Chinese	甜叶桉

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
- Northern Africa
  - Morocco
- Southern Africa
  - Cape Provinces

Australasia click to expand
- Australia
  - South Australia

Northern America click to expand
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000954657
USDA Plants	EUCL
Tropicos	22103329
KEW	urn:lsid:ipni.org:names:592800-1
The Plant List	kew-72677
Open Tree Of Life	179898
Observations.org	117682
NCBI Taxonomy	452569
Nature Serve	2.136102
IUCN Red List	133378591
IPNI	592800-1
iNaturalist	77089
GBIF	3176313
Freebase	/m/099b2w
EPPO	EUCCL
EOL	637218
Calflora (Californian flora)	3533
USDA GRIN	15530
Wikipedia	Eucalyptus_cladocalyx
CMAUP	NPO3809

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_017140615.1	ASM1714061v1	Chromosome	Australian National University	2021-03-09	44.0x	518.87 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

Assessing a potential conflict associated with the production of Moringa oleifera in the Limpopo Province of South Africa: A systems thinking approach

Mashamaite CV, Phiri EE, Mandizvidza TC, Mothapo PN, Pieterse PJ, Albien AJ

Heliyon

22-Feb-2024

PMCID:	PMC10907789
doi:	10.1016/j.heliyon.2024.e26906
PMID:	38434263

Wide Distribution of Teratosphaeria epicoccoides and T. destructans Associated with Diseased Eucalyptus Leaves in Plantations in Southern China

Chen B, Wu W, Chen S

Microorganisms

09-Jan-2024

PMCID:	PMC10819926
doi:	10.3390/microorganisms12010129
PMID:	38257956

Hydraulic segmentation explains differences in loss of branch conductance caused by fire

West AG, Bloy ST, Skelton RP, Midgley JJ

Tree Physiol

06-Sep-2023

PMCID:	PMC10714316
doi:	10.1093/treephys/tpad108
PMID:	37672220

Biosynthesis, herbivore induction, and defensive role of phenylacetaldoxime glucoside

Müller AT, Nakamura Y, Reichelt M, Luck K, Cosio E, Lackus ND, Gershenzon J, Mithöfer A, Köllner TG

Plant Physiol

16-Aug-2023

PMCID:	PMC10756763
doi:	10.1093/plphys/kiad448
PMID:	37584327

Product safety aspects of plant molecular farming

Buyel JF

Front Bioeng Biotechnol

08-Aug-2023

PMCID:	PMC10442644
doi:	10.3389/fbioe.2023.1238917
PMID:	37614627

A review on arsenic in the environment: bio-accumulation, remediation, and disposal

Patel KS, Pandey PK, Martín-Ramos P, Corns WT, Varol S, Bhattacharya P, Zhu Y

RSC Adv

16-May-2023

PMCID:	PMC10186335
doi:	10.1039/d3ra02018e
PMID:	37200696

Breathing Fresh Air in the City: Implementing Avenue Trees as a Sustainable Solution to Reduce Particulate Pollution in Urban Agglomerations

Mandal M, Popek R, Przybysz A, Roy A, Das S, Sarkar A

Plants (Basel)

03-Apr-2023

PMCID:	PMC10097214
doi:	10.3390/plants12071545
PMID:	37050171

Genetic diversity and structure of the 4th cycle breeding population of Chinese fir (Cunninghamia lanceolata (lamb.) hook)

Jing Y, Bian L, Zhang X, Zhao B, Zheng R, Su S, Ye D, Zheng X, El-Kassaby YA, Shi J

Front Plant Sci

27-Jan-2023

PMCID:	PMC9911867
doi:	10.3389/fpls.2023.1106615
PMID:	36778690

Recruitment of distinct UDP‐glycosyltransferase families demonstrates dynamic evolution of chemical defense within Eucalyptus L'Hér

Hansen CC, Sørensen M, Bellucci M, Brandt W, Olsen CE, Goodger JQ, Woodrow IE, Lindberg Møller B, Neilson EH

New Phytol

03-Dec-2022

PMCID:	PMC10107851
doi:	10.1111/nph.18581
PMID:	36305250

Allelopathy and its application as a weed management tool: A review

Khamare Y, Chen J, Marble SC

Front Plant Sci

28-Nov-2022

PMCID:	PMC9742440
doi:	10.3389/fpls.2022.1034649
PMID:	36518508

Antimicrobial Activity of Honey against Oral Microorganisms: Current Reality, Methodological Challenges and Solutions

Romário-Silva D, Alencar SM, Bueno-Silva B, Sardi JD, Franchin M, de Carvalho RD, Ferreira TE, Rosalen PL

Microorganisms

24-Nov-2022

PMCID:	PMC9781356
doi:	10.3390/microorganisms10122325
PMID:	36557578

Engineering medicinal plant-derived CYPs: a promising strategy for production of high-valued secondary metabolites

Sethi A, Bhandawat A, Pati PK

Planta

15-Nov-2022

PMCID:	PMC9664027
doi:	10.1007/s00425-022-04024-9
PMID:	36378350

Diversity of Sporocadaceae (pestalotioid fungi) from Rosa in China

Peng C, Crous PW, Jiang N, Fan XL, Liang YM, Tian CM

Persoonia

13-Aug-2022

PMCID:	PMC10792223
doi:	10.3767/persoonia.2022.49.07
PMID:	38234377

Structure‐guided engineering of key amino acids in UGT85B1 controlling substrate and stereo‐specificity in aromatic cyanogenic glucoside biosynthesis

Del Giudice R, Putkaradze N, dos Santos BM, Hansen CC, Crocoll C, Motawia MS, Fredslund F, Laursen T, Welner DH

Plant J

03-Aug-2022

PMCID:	PMC9545476
doi:	10.1111/tpj.15904
PMID:	35819080

A Review of Commonly Used Methodologies for Assessing the Antibacterial Activity of Honey and Honey Products

Hossain ML, Lim LY, Hammer K, Hettiarachchi D, Locher C

Antibiotics (Basel)

20-Jul-2022

PMCID:	PMC9312033
doi:	10.3390/antibiotics11070975
PMID:	35884229

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben	8434	Click to see CCOC(=O)C1=CC=C(C=C1)O	166.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.4324/9780203219430_CHAPTER_13
p-Anisaldehyde	31244	Click to see COC1=CC=C(C=C1)C=O	136.15	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
Isovanillin	12127	Click to see COC1=C(C=C(C=C1)C=O)O	152.15	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoic acid	5312433	Click to see CCC=CCC=CCC=CCC=CCCC(=O)O	248.36	unknown	via CMAUP database
(R)-2-hydroxypalmitic acid	11065598	Click to see CCCCCCCCCCCCCCC(C(=O)O)O	272.42	unknown	via CMAUP database
2-Keto palmitic acid	5282996	Click to see CCCCCCCCCCCCCCC(=O)C(=O)O	270.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Valeric acid	7991	Click to see CCCCC(=O)O	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(7E,10E,13E)-hexadeca-7,10,13-trienal	14543490	Click to see CCC=CCC=CCC=CCCCCCC=O	234.38	unknown	via CMAUP database
(8E,11E)-heptadeca-8,11-dienal	14543488	Click to see CCCCCC=CCC=CCCCCCCC=O	250.40	unknown	via CMAUP database
(8Z,11Z,14Z)-Heptadecatrienal	6430107	Click to see CCC=CCC=CCC=CCCCCCCC=O	248.40	unknown	via CMAUP database
(8Z,11Z)-Heptadecadienal	6430322	Click to see CCCCCC=CCC=CCCCCCCC=O	250.40	unknown	via CMAUP database
(Z)-8-heptadecenal	6430106	Click to see CCCCCCCCC=CCCCCCCC=O	252.40	unknown	via CMAUP database
8-Heptadecenal	14543489	Click to see CCCCCCCCC=CCCCCCCC=O	252.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid	3931	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Sulfoquinovosylmonoacylglycerols / Sulfoquinovosyl 1-monoacylglycerols
[(2S,3S,4S,5R,6S)-6-[(2R)-3-hexadecanoyloxy-2-hydroxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid	102201401	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CS(=O)(=O)O)O)O)O)O	556.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal	75427	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1080/10412905.1992.9698059
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol	1742129	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	via CMAUP database
(2R)-2,8-Dimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol	12444418	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O	402.70	unknown	via CMAUP database
(2S, 4'S, 8'S)-beta-Tocopherol	76959905	Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O	416.70	unknown	via CMAUP database
(2S)-2,7,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol	73416557	Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picen-4a-yl) formate	58097223	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)OC=O	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13bR)-9-acetyloxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-3a-carboxylic acid	162938413	Click to see CC(=C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O	496.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
9-Acetyloxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-3a-carboxylic acid	162938412	Click to see CC(=C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O	496.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
Cladocalol	21580511	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)OC=O	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018 https://doi.org/10.1002/CHIN.200535206
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	https://doi.org/10.1002/CHIN.200535206
> 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/10.1016/J.PHYTOCHEM.2004.12.018 https://doi.org/10.1002/CHIN.200535206
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/10.1002/CHIN.200535206
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018
Fucosterol	5281328	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Isofucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N	283.24	unknown	via CMAUP database
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Acrylic acids and derivatives / Acrylic acids
Acrylic acid	6581	Click to see C=CC(=O)O	72.06	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3S,6S)-3-Isopropyl-6-methylpiperazine-2,5-dione	13783106	Click to see CC1C(=O)NC(C(=O)N1)C(C)C	170.21	unknown	via CMAUP database
(3S,8aS)-3-Isobutylhexahydropyrrolo[1,2-a]pyrazine-1,4-dione	7074739	Click to see CC(C)CC1C(=O)N2CCCC2C(=O)N1	210.27	unknown	via CMAUP database
cyclo(L-Pro-L-Val)	6992261	Click to see CC(C)C1C(=O)N2CCCC2C(=O)N1	196.25	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Arginyl-Glutamine	7019985	Click to see C(CC(C(=O)NC(CCC(=O)N)C(=O)O)N)CN=C(N)N	302.33	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil	1174	Click to see C1=CNC(=O)NC1=O	112.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Chaetoglobosin Fex	71768077	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(=O)C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O	530.70	unknown	via CMAUP database
Cytoglobosin A	46209792	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CC4C1C(=C(C4=O)O)C)C(=O)NC3CC5=CNC6=CC=CC=C65)C)O	528.60	unknown	via CMAUP database
Cytoglobosin B	46209793	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O	530.70	unknown	via CMAUP database
Cytoglobosin C	44610809	Click to see CC1CC=CC2C(C(=C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C)O	530.70	unknown	via CMAUP database
Cytoglobosin D	46209919	Click to see CC1CC=CC2C=C(C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C	514.70	unknown	via CMAUP database
Cytoglobosin E	46209920	Click to see CC1CC=CC2C=C(C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)CO	528.60	unknown	via CMAUP database
Cytoglobosin F	46209921	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O	530.70	unknown	via CMAUP database
Cytoglobosin G	46209922	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O	532.70	unknown	via CMAUP database
isochaetoglobosin D	23259926	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O	528.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde	637511	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eucalyptin	76573	Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)OC)O	326.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.018 https://doi.org/10.1002/CHIN.200535206

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Eucalyptus cladocalyx

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