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Eucalyptus brassiana

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644039edbcc2f738889159
Scientific name Eucalyptus brassiana
Authority S.T.Blake
First published in Austrobaileya 1: 1 (1977)

Description Top

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Eucalyptus brassiana, also known as Cape York gum, is a tree native to northern Queensland and Papua New Guinea. It can reach heights of up to 20 meters and has rough, dark bark on the trunk and smooth grey bark on the branches. The leaves are lance-shaped and glossy green, and the tree produces white flowers and small woody fruit. This species was first described in 1977 and is named after botanist Leonard John Brass. It is found in woodland and open forest habitats in the Cape York Peninsula and parts of Papua New Guinea.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 褐桉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000954544
Tropicos 100187530
KEW urn:lsid:ipni.org:names:592751-1
The Plant List kew-72563
PFAF Eucalyptus brassiana
Open Tree Of Life 275268
NCBI Taxonomy 183814
IUCN Red List 133378234
IPNI 592751-1
GBIF 3176392
EPPO EUCBN
EOL 230405
Wikipedia Eucalyptus_brassiana

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
Endophytic species of Induratia from coffee and carqueja plants from Brazil and its potential for the biological control of toxicogenic fungi on coffee beans by means of antimicrobial volatiles Gomes AA, Paes SA, Ferreira AP, Pinho DB, de Lourdes Cardeal Z, Menezes HC, Cardoso PG, Pereira OL Braz J Microbiol 04-Jan-2023
PMCID:PMC9944607
doi:10.1007/s42770-022-00887-y
PMID:36598751
Arbuscular Mycorrhizal Fungi and Soil Quality Indicators in Eucalyptus genotypes With Different Drought Tolerance Levels Lopes BA, Silva AM, Santana MC, Feiler HP, Pereira AP, Teixeira MF, de Araújo VL, de Ávila PA, Gonçalves JL, Staunton S, Cardoso EJ Front Fungal Biol 20-Jun-2022
PMCID:PMC10512215
doi:10.3389/ffunb.2022.913570
PMID:37746223
Reconsideration of species boundaries and proposed DNA barcodes for Calonectria Liu QL, Li JQ, Wingfield MJ, Duong TA, Wingfield BD, Crous PW, Chen SF Stud Mycol 07-Oct-2020
PMCID:PMC8295567
doi:10.1016/j.simyco.2020.08.001
PMID:34322181
Foliar pathogens of eucalypts Crous PW, Wingfield MJ, Cheewangkoon R, Carnegie AJ, Burgess TI, Summerell BA, Edwards J, Taylor PW, Groenewald JZ Stud Mycol 08-Aug-2019
PMCID:PMC6797021
doi:10.1016/j.simyco.2019.08.001
PMID:31636729
The Eucalyptus Cuticular Waxes Contribute in Preformed Defense Against Austropuccinia psidii dos Santos IB, Lopes MD, Bini AP, Tschoeke BA, Verssani BA, Figueredo EF, Cataldi TR, Marques JP, Silva LD, Labate CA, Quecine MC Front Plant Sci 09-Jan-2019
PMCID:PMC6334236
doi:10.3389/fpls.2018.01978
PMID:30687371
Fungal Planet description sheets: 785–867 Crous PW, Luangsa-ard JJ, Wingfield MJ, Carnegie AJ, Hernández-Restrepo M, Lombard L, Roux J, Barreto RW, Baseia IG, Cano-Lira JF, Martín MP, Morozova OV, Stchigel AM, Summerell BA, Brandrud TE, Dima B, García D, Giraldo A, Guarro J, Gusmão LF, Khamsuntorn P, Noordeloos ME, Nuankaew S, Pinruan U, Rodríguez-Andrade E, Souza-Motta CM, Thangavel R, van Iperen AL, Abreu VP, Accioly T, Alves JL, Andrade JP, Bahram M, Baral HO, Barbier E, Barnes CW, Bendiksen E, Bernard E, Bezerra JD, Bezerra JL, Bizio E, Blair JE, Bulyonkova TM, Cabral TS, Caiafa MV, Cantillo T, Colmán AA, Conceição LB, Cruz S, Cunha AO, Darveaux BA, da Silva AL, da Silva GA, da Silva GM, da Silva RM, de Oliveira RJ, Oliveira RL, De Souza JT, Dueñas M, Evans HC, Epifani F, Felipe MT, Fernández-López J, Ferreira BW, Figueiredo CN, Filippova NV, Flores JA, Gené J, Ghorbani G, Gibertoni TB, Glushakova AM, Healy R, Huhndorf SM, Iturrieta-González I, Javan-Nikkhah M, Juciano RF, Jurjević Ž, Kachalkin AV, Keochanpheng K, Krisai-Greilhuber I, Li YC, Lima AA, Machado AR, Madrid H, Magalhães OM, Marbach PA, Melanda GC, Miller AN, Mongkolsamrit S, Nascimento RP, Oliveira TG, Ordoñez ME, Orzes R, Palma MA, Pearce CJ, Pereira OL, Perrone G, Peterson SW, Pham TH, Piontelli E, Pordel A, Quijada L, Raja HA, Rosas de Paz E, Ryvarden L, Saitta A, Salcedo SS, Sandoval-Denis M, Santos TA, Seifert KA, Silva BD, Smith ME, Soares AM, Sommai S, Sousa JO, Suetrong S, Susca A, Tedersoo L, Telleria MT, Thanakitpipattana D, Valenzuela-Lopez N, Visagie CM, Zapata M, Groenewald JZ Persoonia 14-Dec-2018
PMCID:PMC6344811
doi:10.3767/persoonia.2018.41.12
PMID:30728607
Communally Nesting Migratory Birds Create Ecological Hot-Spots in Tropical Australia Natusch DJ, Lyons JA, Brown G, Shine R PLoS One 05-Oct-2016
PMCID:PMC5051721
doi:10.1371/journal.pone.0162651
PMID:27706197
Revising the Schizoparmaceae: Coniella and its synonyms Pilidiella and Schizoparme Alvarez LV, Groenewald JZ, Crous PW Stud Mycol 23-Sep-2016
PMCID:PMC5066162
doi:10.1016/j.simyco.2016.09.001
PMID:27766001
Transcriptionally active LTR retrotransposons in Eucalyptus genus are differentially expressed and insertionally polymorphic Marcon HS, Domingues DS, Silva JC, Borges RJ, Matioli FF, de Mattos Fontes MR, Marino CL BMC Plant Biol 14-Aug-2015
PMCID:PMC4535378
doi:10.1186/s12870-015-0550-1
PMID:26268941
Fungal Planet description sheets: 320–370 Crous PW, Wingfield MJ, Guarro J, Hernández-Restrepo M, Sutton DA, Acharya K, Barber PA, Boekhout T, Dimitrov RA, Dueñas M, Dutta AK, Gené J, Gouliamova DE, Groenewald M, Lombard L, Morozova OV, Sarkar J, Smith MT, Stchigel AM, Wiederhold NP, Alexandrova AV, Antelmi I, Armengol J, Barnes I, Cano-Lira JF, Castañeda Ruiz RF, Contu M, Courtecuisse PR, da Silveira AL, Decock CA, de Goes A, Edathodu J, Ercole E, Firmino AC, Fourie A, Fournier J, Furtado EL, Geering AD, Gershenzon J, Giraldo A, Gramaje D, Hammerbacher A, He XL, Haryadi D, Khemmuk W, Kovalenko AE, Krawczynski R, Laich F, Lechat C, Lopes UP, Madrid H, Malysheva EF, Marín-Felix Y, Martín MP, Mostert L, Nigro F, Pereira OL, Picillo B, Pinho DB, Popov ES, Rodas Peláez CA, Rooney-Latham S, Sandoval-Denis M, Shivas RG, Silva V, Stoilova-Disheva MM, Telleria MT, Ullah C, Unsicker SB, van der Merwe NA, Vizzini A, Wagner HG, Wong PT, Wood AR, Groenewald JZ Persoonia 10-Jun-2015
PMCID:PMC4510277
doi:10.3767/003158515X688433
PMID:26240451
Diversity and potential impact of Calonectria species in Eucalyptus plantations in Brazil Alfenas RF, Lombard L, Pereira OL, Alfenas AC, Crous PW Stud Mycol 23-Jan-2015
PMCID:PMC4779794
doi:10.1016/j.simyco.2014.11.002
PMID:26955192
Chemical Constituents of the Leaf Essential Oil of<i>Eucalyptus brassiana</i>S. T. Blake A. K. Singh, K. C. Gupta, J. J. Brophy Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1991.9697906

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
> 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/10.1080/10412905.1991.9697906
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1080/10412905.1991.9697906
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1991.9697906
o-Methoxy-o-methyl-p-allylphenol 45266909 Click to see CC1=CC(=CC(=C1O)OC)CC=C 178.23 unknown https://doi.org/10.1080/10412905.1991.9697906
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
cis-5-Octenoic acid 5282718 Click to see CCC=CCCCC(=O)O 142.20 unknown https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.1991.9697906
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
> 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 https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Pinene 15837102 Click to see CC1=C2CC(C2(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
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/10.1080/10412905.1991.9697906
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9697906
Delta-Terpineol 81722 Click to see CC(C)(C1CCC(=C)CC1)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697906
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697906
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697906
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697906
> 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/10.1080/10412905.1991.9697906
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697906
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697906
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697906
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697906
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9697906
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1991.9697906
> 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/10.1080/10412905.1991.9697906
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool, oxide 102611 Click to see CC(=CCCC(C)(C1CO1)O)C 170.25 unknown https://doi.org/10.1080/10412905.1991.9697906
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde 11552 Click to see CC(C)CC=O 86.13 unknown https://doi.org/10.1080/10412905.1991.9697906

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