Language	Common/alternative name
Arabic	أوكالبتوس بيضوي
Bulgarian	яйцевиден евкалипт
Russian	Эвкалипт яйцевидный
Ukrainian	Евкаліпт яйцеподібний
Chinese	卵叶桉

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Eucalyptus ovata subsp. ovata		-

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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
- Macaronesia
  - Canary Islands

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Tasmania
  - Victoria
- New Zealand
  - New Zealand North

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000955524
USDA Plants	EUOV2
Tropicos	100188267
INPN	611715
KEW	urn:lsid:ipni.org:names:593197-1
The Plant List	kew-73534
Open Tree Of Life	566584
NCBI Taxonomy	155760
IUCN Red List	133376701
IPNI	593197-1
iNaturalist	323789
GBIF	3177130
Freebase	/m/02qfvtk
EPPO	EUCOV
EOL	245550
USDA GRIN	401264
Wikipedia	Eucalyptus_ovata
CMAUP	NPO18413

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 influence of stormwater infiltration on downslope groundwater chemistry

Arora M, Fletcher TD, Burns MJ, Western AW, Yong CF, Poelsma PJ, James RB

Environ Geochem Health

30-Aug-2023

PMCID:	PMC10611863
doi:	10.1007/s10653-023-01732-3
PMID:	37646920

The Effect of the Height of Coppicing and Harvest Season on the Yield and Quality of the Essential Oil of Kunzea ambigua

Park C, Garland SM, Close DC

Plants (Basel)

20-Dec-2022

PMCID:	PMC9824379
doi:	10.3390/plants12010020
PMID:	36616149

The survival, development, and reproduction of Gonipterus platensis (Coleoptera: Curculionidae) on the main Eucalyptus (Myrtaceae) genotypes planted in Brazil

de Oliveira NC, Ribeiro MF, Ottati A, Tavares WD, Serrão JE, Zanuncio JC, Zanetti R, Wilcken CF

PeerJ

01-Aug-2022

PMCID:	PMC9351619
doi:	10.7717/peerj.13698
PMID:	35935252

Leaf Economic and Hydraulic Traits Signal Disparate Climate Adaptation Patterns in Two Co-Occurring Woodland Eucalypts

Prober SM, Potts BM, Harrison PA, Wiehl G, Bailey TG, Costa e Silva J, Price MR, Speijers J, Steane DA, Vaillancourt RE

Plants (Basel)

14-Jul-2022

PMCID:	PMC9320154
doi:	10.3390/plants11141846
PMID:	35890479

Effectiveness of plants and green infrastructure utilization in ambient particulate matter removal

Wróblewska K, Jeong BR

Environ Sci Eur

25-Sep-2021

PMCID:	PMC8475335
doi:	10.1186/s12302-021-00547-2
PMID:	34603905

Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections

Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM

Plants (Basel)

04-Jul-2021

PMCID:	PMC8309379
doi:	10.3390/plants10071367
PMID:	34371570

When taxonomy and biological control researchers unite: Species delimitation of Eadya parasitoids (Braconidae) and consequences for classical biological control of invasive paropsine pests of Eucalyptus

Peixoto L, Allen GR, Ridenbaugh RD, Quarrell SR, Withers TM, Sharanowski BJ

PLoS One

16-Aug-2018

PMCID:	PMC6095507
doi:	10.1371/journal.pone.0201276
PMID:	30114194

The role of hybridization in facilitating tree invasion

Gaskin JF

AoB Plants

26-Dec-2016

PMCID:	PMC5391693
doi:	10.1093/aobpla/plw079
PMID:	28028055

An overview of Australia’s Phytophthora species assemblage in natural ecosystems recovered from a survey in Victoria

Dunstan WA, Howard K, StJ. Hardy GE, Burgess TI

IMA Fungus

02-Mar-2016

PMCID:	PMC4941687
doi:	10.5598/imafungus.2016.07.01.04
PMID:	27433440

The Relative Concentrations of Nutrients and Toxins Dictate Feeding by a Vertebrate Browser, the Greater Glider Petauroides volans

Jensen LM, Wallis IR, Foley WJ

PLoS One

04-May-2015

PMCID:	PMC4418660
doi:	10.1371/journal.pone.0121584
PMID:	25938422

Leaders benefit followers in the collective movement of a social sawfly

Hodgkin LK, Symonds MR, Elgar MA

Proc Biol Sci

07-Dec-2014

PMCID:	PMC4213643
doi:	10.1098/rspb.2014.1700
PMID:	25320163

A taxonomic and phylogenetic revision of Penicillium section Aspergilloides

Houbraken J, Visagie CM, Meijer M, Frisvad JC, Busby PE, Pitt JI, Seifert KA, Louis-Seize G, Demirel R, Yilmaz N, Jacobs K, Christensen M, Samson RA

Stud Mycol

22-Sep-2014

PMCID:	PMC4255628
doi:	10.1016/j.simyco.2014.09.002
PMID:	25492984

Tree-hugging koalas demonstrate a novel thermoregulatory mechanism for arboreal mammals

Briscoe NJ, Handasyde KA, Griffiths SR, Porter WP, Krockenberger A, Kearney MR

Biol Lett

01-Jun-2014

PMCID:	PMC4090547
doi:	10.1098/rsbl.2014.0235
PMID:	24899683

Natural Treatment Systems as Sustainable Ecotechnologies for the Developing Countries

Mahmood Q, Pervez A, Zeb BS, Zaffar H, Yaqoob H, Waseem M, Zahidullah, Afsheen S

Biomed Res Int

26-Jun-2013

PMCID:	PMC3708409
doi:	10.1155/2013/796373
PMID:	23878819

A remarkable case of mosaic parapatry in millipedes

Mesibov R

Zookeys

20-Dec-2011

PMCID:	PMC3253572
doi:	10.3897/zookeys.156.1893
PMID:	22303096

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
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein	5281243	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(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1007/BF00714930
Super Squalene; trans-Squalene;AddaVax	1105	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Aminobutanoate	6992099	Click to see C(CC(=O)[O-])C[NH3+]	103.12	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
4-Allyloxycoumarin	5133468	Click to see C=CCOC1=CC(=O)OC2=CC=CC=C21	202.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnin	439499	Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O	340.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Gallocatechin-(4alpha->6)-(+)-catechin	72193636	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
(+)-Gallocatechin-(4alpha->8)-(+)-catechin	13831063	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
[Gallocatechin-(4alpha->8)]2-catechin	14890508	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	898.80	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
2-(3,4-dihydroxyphenyl)-6-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	13831069	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Endotelon	130556	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Epigallocatechin-(4beta->8)-catechin	13831061	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	594.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Procyanidin B1	11250133	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Procyanidin B3	146798	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Prodelphinidin B	5089687	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Prodelphinidin C2	71623698	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	898.80	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechingallate	367141	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
(+)-Catechin gallate	5276454	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Flavan-3,3',4',5,5',7-hexol	1249	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
8-(2-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)-4',5,7-trihydroxy-3'-methoxyflavone	101429641	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3',4',5,7-Tetrahydroxy-6-(beta-D-glucopyranosyloxy)flavone	5459939	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14055723	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O	616.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one	5317364	Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308704	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside	5491814	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O	616.50	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Quercetin 3-O-beta-D-arabinofuranoside	5320668	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4',5-Dihydroxy-3',8-dimethoxy-7-(beta-D-glucopyranosyloxy)flavone	14825846	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)OC)O	492.40	unknown	via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one	86573698	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O	608.50	unknown	via CMAUP database
Luteolin 7-rutinoside	10461109	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	594.50	unknown	via CMAUP database
Thermopsoside	11294177	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	via CMAUP database
Tricin 7-(6-rhamnosyl)glucoside	100925474	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O)O	638.60	unknown	via CMAUP database
Tricin 7-glucoside	5322022	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	492.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
4',5,7-Trihydroxy-8-(beta-D-glucopyranosyloxy)flavone	6420079	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
8-(beta-D-Glucopyranosyloxy)-4',5,7-trihydroxy-3'-methoxyflavone	101288288	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	via CMAUP database
Hypolaetin-8-glucoside	5318255	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Vitexin-4invertedexclamationmarka-o-glucoside	57387656	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
6-Hydroxy-5,7,8-trimethyl-2,10,19-trioxa-15-azatetracyclo[10.5.1.15,8.015,18]nonadec-12-ene-3,9-dione	85189098	Click to see CC1C(C2(CC(=O)OC3CCN4C3C(=CC4)COC(=O)C1(O2)C)C)O	351.40	unknown	https://doi.org/10.1016/S0367-326X(00)00298-7

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Eucalyptus ovata

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

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