Language	Common/alternative name
English	white ironbark
Spanish	yellow gum
Arabic	أوكالبتوس أبيض الخشب
Azerbaijani	ağ oduncaqlı evkalipt
German	weißer gummi-eukalyptus
Hebrew	אקליפטוס בהיר קליפה
Upper Sorbian	běły gumijowc
Russian	Эвкалипт белодревесный
Swedish	storfruktig blåeukalyptus
Swedish	blåeukalyptus
Chinese	白木桉
Chinese	黃橡膠樹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Eucalyptus leucoxylon subsp. bellarinensis	Rule	Muelleria 11: 133 (1998)
Eucalyptus leucoxylon subsp. leucoxylon	F.Muell.	-
Eucalyptus leucoxylon subsp. megalocarpa	Boland	Austral. Forest. Res. 9: 68 (1979)
Eucalyptus leucoxylon subsp. pruinosa	(F.Muell. ex Miq.) Boland	Austral. Forest. Res. 9: 68 (1979)

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

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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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Victoria

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000955243
USDA Plants	EULE13
Tropicos	22103334
INPN	445830
KEW	urn:lsid:ipni.org:names:593070-1
The Plant List	kew-73247
Open Tree Of Life	505242
NCBI Taxonomy	34318
IUCN Red List	131215202
IPNI	593070-1
iNaturalist	339974
GBIF	3177019
Freebase	/m/02qlj81
EOL	301411
Calflora (Californian flora)	12491
USDA GRIN	15941
Wikipedia	Eucalyptus_leucoxylon

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

The Effect of Surrounding Vegetation on Basal Stem Measurements Acquired Using Low-Cost Depth Sensors in Urban and Native Forest Environments

McGlade J, Wallace L, Hally B, Reinke K, Jones S

Sensors (Basel)

12-Apr-2023

PMCID:	PMC10143225
doi:	10.3390/s23083933
PMID:	37112278

Seasonal Phenology and Climate Associated Feeding Activity of Introduced Marchalina hellenica in Southeast Australia

Jaroslow DD, Cunningham JP, Smith DI, Steinbauer MJ

Insects

21-Mar-2023

PMCID:	PMC10054368
doi:	10.3390/insects14030305
PMID:	36975990

Co-developing an international TLS network for the 3D ecological understanding of global trees: System architecture, remote sensing models, and functional prospects

Lin Y, Filin S, Billen R, Mizoue N

Environ Sci Ecotechnol

21-Feb-2023

PMCID:	PMC10024182
doi:	10.1016/j.ese.2023.100257
PMID:	36941885

Individuality and stability of the koala (Phascolarctos cinereus) faecal microbiota through time

Eisenhofer R, Brice KL, Blyton MD, Bevins SE, Leigh K, Singh BK, Helgen KM, Hough I, Daniels CB, Speight N, Moore BD

PeerJ

23-Jan-2023

PMCID:	PMC9879153
doi:	10.7717/peerj.14598
PMID:	36710873

Sun-Safe Zones: Investigating Integrated Shading Strategies for Children’s Play Areas in Urban Parks

Cherian NC, Subasinghe C

Int J Environ Res Public Health

22-Dec-2022

PMCID:	PMC9819332
doi:	10.3390/ijerph20010114
PMID:	36612436

Synthesis and characterization of plant extracted silver nanoparticles and advances in dental implant applications

Hossain N, Islam MA, Chowdhury MA

Heliyon

10-Dec-2022

PMCID:	PMC9794905
doi:	10.1016/j.heliyon.2022.e12313
PMID:	36590472

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

Impact of genus (Geotrigona, Melipona, Scaptotrigona) in the targeted 1H-NMR organic profile, and authenticity test by interphase emulsion of honey processed in cerumen pots by stingless bees in Ecuador

Vit P, van der Meulen J, Diaz M, Pedro SR, Esperança I, Zakaria R, Beckh G, Maza F, Meccia G, Engel MS

Curr Res Food Sci

12-Nov-2022

PMCID:	PMC9947262
doi:	10.1016/j.crfs.2022.11.005
PMID:	36846470

When aggressiveness could be too risky: linking personality traits and predator response in superb fairy-wrens

Bilby J, Colombelli-Négrel D, Katsis AC, Kleindorfer S

PeerJ

28-Sep-2022

PMCID:	PMC9526405
doi:	10.7717/peerj.14011
PMID:	36193436

Multifarious global flora fabricated phytosynthesis of silver nanoparticles: a green nanoweapon for antiviral approach including SARS-CoV-2

Karthik C, Punnaivalavan KA, Prabha SP, Caroline DG

Int Nano Lett

12-Feb-2022

PMCID:	PMC8853038
doi:	10.1007/s40089-022-00367-z
PMID:	35194512

In Vitro Potential of Clary Sage and Coriander Essential Oils as Crop Protection and Post-Harvest Decay Control Products

Raveau R, Fontaine J, Soltani A, Mediouni Ben Jemâa J, Laruelle F, Lounès-Hadj Sahraoui A

Foods

24-Jan-2022

PMCID:	PMC8834200
doi:	10.3390/foods11030312
PMID:	35159462

Antiviral Activities of Eucalyptus Essential Oils: Their Effectiveness as Therapeutic Targets against Human Viruses

Mieres-Castro D, Ahmar S, Shabbir R, Mora-Poblete F

Pharmaceuticals (Basel)

23-Nov-2021

PMCID:	PMC8706319
doi:	10.3390/ph14121210
PMID:	34959612

Can Eucalyptol Replace Antibiotics?

Mączka W, Duda-Madej A, Górny A, Grabarczyk M, Wińska K

Molecules

14-Aug-2021

PMCID:	PMC8398027
doi:	10.3390/molecules26164933
PMID:	34443521

Why Variation in Flower Color May Help Reproductive Success in the Endangered Australian Orchid Caladenia fulva

Basist G, Dyer AG, Garcia JE, Raleigh RE, Lawrie AC

Front Plant Sci

09-Feb-2021

PMCID:	PMC7899986
doi:	10.3389/fpls.2021.599874
PMID:	33633758

Dataset of leaf inclination angles for 71 different Eucalyptus species

Pisek J, Adamson K

Data Brief

09-Oct-2020

PMCID:	PMC7569295
doi:	10.1016/j.dib.2020.106391
PMID:	33102658

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
> Benzenoids / Benzene and substituted derivatives
2-Phenylethyl propionate	31225	Click to see CCC(=O)OCCC1=CC=CC=C1	178.23	unknown	https://doi.org/10.1002/FFJ.2730100605
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	https://doi.org/10.1002/FFJ.2730100605
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Isoamyl isovalerate	12613	Click to see CC(C)CCOC(=O)CC(C)C	172.26	unknown	https://doi.org/10.1002/FFJ.2730100605
Isobutyl isovalerate	11514	Click to see CC(C)CC(=O)OCC(C)C	158.24	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1002/FFJ.2730100605
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
alpha-Fenchene	28930	Click to see CC1(C2CCC1C(=C)C2)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730100605
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730100605
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6S)-rel-	85567	Click to see CC1=CC(C(CC1)C(C)C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730100605
Delta-Terpineol	81722	Click to see CC(C)(C1CCC(=C)CC1)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Piperitone	6987	Click to see CC1=CC(=O)C(CC1)C(C)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730100605
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1002/FFJ.2730100605
trans-Piperitol	85568	Click to see CC1=CC(C(CC1)C(C)C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Eudesma-5,7(11)-diene	6428860	Click to see CC1CCCC2(C1=CC(=C(C)C)CC2)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315594	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1002/FFJ.2730100605
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1002/FFJ.2730100605
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
beta-Cubebene	93081	Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Globulol	101716	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
Palustrol	110745	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
Viridiflorol (incomplete stereochemistry)	94174	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene	5315347	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
> 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	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene	10123	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730100605
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730100605
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1007/BF00714930
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol	5991	Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O	296.40	unknown	https://doi.org/10.1002/FFJ.2730100605
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-2-phenyl-2-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyacetonitrile	154497290	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.018
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
4-Isopropyl-2-cyclohexenone	92780	Click to see CC(C)C1CCC(=O)C=C1	138.21	unknown	https://doi.org/10.1002/FFJ.2730100605
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Torquatone	256516	Click to see CC1=C(C(=C(C(=C1OC)C(=O)CC(C)C)OC)C)OC	280.36	unknown	https://doi.org/10.1002/FFJ.2730100605

Biological Material Top

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Eucalyptus leucoxylon

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