Eucalyptus cloeziana - Unknown
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Details Top

Internal ID UUID644039f4c078d438900877
Scientific name Eucalyptus cloeziana
Authority F.Muell.
First published in Fragm. 11: 44 (1878)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eucalyptus stannariensis F.M.Bailey Queensland Agric. J. 21: 293 (1908)

Common names Top

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Language Common/alternative name
English cloeziana gum
English dead finish
English gympie messmate
Chinese 大花序桉

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Rwanda

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000954668
USDA Plants EUCL6
Tropicos 100187620
KEW urn:lsid:ipni.org:names:592804-1
The Plant List kew-72687
Open Tree Of Life 1031160
NCBI Taxonomy 34320
IUCN Red List 61909907
IPNI 592804-1
iNaturalist 1074794
GBIF 3176995
Freebase /m/02qhkf9
EPPO EUCCZ
EOL 630204
USDA GRIN 15876
Wikipedia Eucalyptus_cloeziana

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014182715.1 ASM1418271v1 Chromosome Australian National University 2020-08-14 32.0x 457.84 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Meloidogyne spp. in Eucalypts - Reproduction and Damage to Seedling Growth Lopes Vieira JO Júnior, Cunha Pereira R, Mangeiro MZ, Moreira Souza R J Nematol 23-Jan-2024
PMCID:PMC10805518
doi:10.2478/jofnem-2023-0059
PMID:38264460
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Changes in the physiological activity of parenchyma cells in Dalbergia odorifera xylem and its relationship with heartwood formation Ma R, Luo J, Wang W, Fu Y BMC Plant Biol 14-Nov-2023
PMCID:PMC10644609
doi:10.1186/s12870-023-04592-2
PMID:37957552
How does leaf succulence relate to plant drought resistance in woody shrubs? Guo B, Arndt SK, Miller RE, Szota C, Farrell C Tree Physiol 19-May-2023
PMCID:PMC10652328
doi:10.1093/treephys/tpad066
PMID:37208014
Genetic Diversity Analysis and Core Germplasm Collection Construction of Camellia oleifera Based on Fruit Phenotype and SSR Data Zhu Y, Liang D, Song Z, Tan Y, Guo X, Wang D Genes (Basel) 13-Dec-2022
PMCID:PMC9777545
doi:10.3390/genes13122351
PMID:36553618
Genetic Diversity Analysis of Sapindus in China and Extraction of a Core Germplasm Collection Using EST-SSR Markers Liu J, Gao S, Xu Y, Wang M, Ngiam JJ, Rui Wen NC, Yi JJ, Weng X, Jia L, Salojärvi J Front Plant Sci 24-May-2022
PMCID:PMC9171133
doi:10.3389/fpls.2022.857993
PMID:35685004
Generic boundaries in the Ophiostomatales reconsidered and revised de Beer ZW, Procter M, Wingfield MJ, Marincowitz S, Duong TA Stud Mycol 30-Mar-2022
PMCID:PMC9365045
doi:10.3114/sim.2022.101.02
PMID:36059894
Temperature responses of photosynthesis and respiration in evergreen trees from boreal to tropical latitudes Crous KY, Uddling J, De Kauwe MG New Phytol 30-Jan-2022
PMCID:PMC9994441
doi:10.1111/nph.17951
PMID:35007351
Selection of a core collection of Prunus sibirica L. germplasm by a stepwise clustering method using simple sequence repeat markers Sun Y, Dong S, Liu Q, Chen J, Pan J, Zhang J PLoS One 19-Nov-2021
PMCID:PMC8604298
doi:10.1371/journal.pone.0260097
PMID:34797843
Genetic Diversity of a Natural Population of Akebia trifoliata (Thunb.) Koidz and Extraction of a Core Collection Using Simple Sequence Repeat Markers Zhong Y, Wang Y, Sun Z, Niu J, Shi Y, Huang K, Chen J, Chen J, Luan M Front Genet 31-Aug-2021
PMCID:PMC8438410
doi:10.3389/fgene.2021.716498
PMID:34531899
Use of polylactic acid microvessel to obtain microplantlets of Eucalyptus microcorys through indirect organogenesis Faria JC, Terra JA, Molinari LV, Delarmelina WM, Ribeiro-Kumara C, de Sena Neto AR, de Carvalho D, Brondani GE 3 Biotech 05-Jul-2021
PMCID:PMC8257825
doi:10.1007/s13205-021-02822-8
PMID:34290947
Molecular relationships of Campomanesia xanthocarpa within Myrtaceae based on the complete plastome sequence and on the plastid ycf2 gene Machado LD, Vieira LD, Stefenon VM, Faoro H, Pedrosa FD, Guerra MP, Nodari RO Genet Mol Biol 10-Jun-2020
PMCID:PMC7288672
doi:10.1590/1678-4685-GMB-2018-0377
PMID:32555941
The Genera of Fungi – G6: Arthrographis, Kramasamuha, Melnikomyces, Thysanorea, and Verruconis Hernández-Restrepo M, Giraldo A, van Doorn R, Wingfield MJ, Groenewald JZ, Barreto RW, Colmán AA, Mansur PS, Crous PW Fungal Syst Evol 05-Feb-2020
PMCID:PMC7451779
doi:10.3114/fuse.2020.06.01
PMID:32904189
Blastacervulus metrosideri sp. nov. leaf spot on Metrosideros excelsa in New Zealand Johnston PR, Park D Fungal Syst Evol 15-Mar-2019
PMCID:PMC7235978
doi:10.3114/fuse.2019.03.09
PMID:32467901
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

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/10.1080/10412905.1990.9697829
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
> 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/10.1080/10412905.1990.9697829
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
> 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/10.1080/10412905.1990.9697829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1990.9697829
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1990.9697829
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1990.9697829
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1990.9697829
(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/10.1080/10412905.1990.9697829
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1990.9697829
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1990.9697829
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1990.9697829
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1990.9697829
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / M-benzoquinones
Tasmanone 12443231 Click to see CC1=C(C(C(=O)C(C1=O)C(=O)C(C)C)(C)C)OC 252.31 unknown https://doi.org/10.1080/10412905.1990.9697829

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