Eucalyptus delegatensis - Unknown
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Internal ID UUID644039fcd2f81444980762
Scientific name Eucalyptus delegatensis
Authority R.T.Baker
First published in Proc. Linn. Soc. New South Wales 25: 305 (1900)

Description Top

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Eucalyptus delegatensis, also known as alpine ash, is a tree species native to southeastern Australia. It can grow up to 90 meters tall and has a straight trunk with rough bark on the lower half and smooth white bark on the upper half. The leaves are lance-shaped and the flowers are white. This species was first described in 1900 and has two recognized subspecies. It is commonly found in subalpine forests and can form pure stands. Its distribution ranges from New South Wales and the Australian Capital Territory to Tasmania.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English alpine-ash
Spanish ceniza alpina
Chinese 大桉
Chinese 代表桉
Chinese 巨桉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus delegatensis subsp. delegatensis R.T.Baker -
Eucalyptus delegatensis subsp. tasmaniensis Boland Austral. Forest. Res. 15: 177 (1985)

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
  • Australasia
    • Australia
      • New South Wales
      • Tasmania
      • Victoria
    • New Zealand
      • New Zealand North
      • New Zealand South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000954798
USDA Plants EUDE13
Tropicos 100187716
INPN 611735
KEW urn:lsid:ipni.org:names:592873-1
The Plant List kew-72810
Open Tree Of Life 771613
NCBI Taxonomy 87669
IUCN Red List 61912169
IPNI 592873-1
iNaturalist 323289
GBIF 3176597
Freebase /m/0348z6
EPPO EUCDE
EOL 631998
USDA GRIN 15894
Wikipedia Eucalyptus_delegatensis

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
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
Two new species of Phaeohelotium (Leotiomycetes: Helotiaceae) from Chile and their putative ectomycorrhizal status Grupe II AC, Smith ME, Weier A, Healy R, Caiafa MV, Pfister DH, Haelewaters D, Quandt CA Fungal Syst Evol 15-Dec-2022
PMCID:PMC9875694
doi:10.3114/fuse.2022.10.10
PMID:36741556
Forest restoration in a time of fire: perspectives from tall, wet eucalypt forests subject to stand-replacing wildfires Lindenmayer DB, Bowd EJ, Gibbons P Philos Trans R Soc Lond B Biol Sci 14-Nov-2022
PMCID:PMC9661950
doi:10.1098/rstb.2021.0082
PMID:36373929
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
Effect of bending on radial distribution density, MFA and MOE of bent bamboo Wang X, Ma J, Xu W, Fei B, Lian C, Sun F Sci Rep 21-May-2022
PMCID:PMC9124210
doi:10.1038/s41598-022-12675-7
PMID:35597801
An assessment of ectoparasites across highland and lowland populations of Leadbeater's possum (Gymnobelideus leadbeateri): Implications for genetic rescue translocations Steventon C, Harley D, Wicker L, Legione AR, Devlin JM, Hufschmid J Int J Parasitol Parasites Wildl 10-May-2022
PMCID:PMC9108725
doi:10.1016/j.ijppaw.2022.05.002
PMID:35586791
Multi-decadal increase of forest burned area in Australia is linked to climate change Canadell JG, Meyer CP, Cook GD, Dowdy A, Briggs PR, Knauer J, Pepler A, Haverd V Nat Commun 26-Nov-2021
PMCID:PMC8626427
doi:10.1038/s41467-021-27225-4
PMID:34836974
Natural disturbances and masting: from mechanisms to fitness consequences Vacchiano G, Pesendorfer MB, Conedera M, Gratzer G, Rossi L, Ascoli D Philos Trans R Soc Lond B Biol Sci 18-Oct-2021
PMCID:PMC8520777
doi:10.1098/rstb.2020.0384
PMID:34657468
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia Lebel T, Douch J, Tegart L, Vaughan L, Cooper JA, Nuytinck J Persoonia 03-Aug-2021
PMCID:PMC10784664
doi:10.3767/persoonia.2023.47.01
PMID:38352975
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia Lebel T, Douch J, Tegart L, Vaughan L, Cooper JA, Nuytinck J Persoonia 03-Aug-2021
PMCID:PMC10486632
doi:10.3767/persoonia.2021.47.01
PMID:37693797
Temporal patterns of forest seedling emergence across different disturbance histories Bowd EJ, McBurney L, Blair DP, Lindenmayer DB Ecol Evol 26-Jun-2021
PMCID:PMC8293764
doi:10.1002/ece3.7568
PMID:34306621
Molecular reassessment of diaporthalean fungi associated with strawberry, including the leaf blight fungus, Paraphomopsis obscurans gen. et comb. nov. (Melanconiellaceae) Udayanga D, Miriyagalla SD, Manamgoda DS, Lewers KS, Gardiennet A, Castlebury LA IMA Fungus 22-Jun-2021
PMCID:PMC8218473
doi:10.1186/s43008-021-00069-9
PMID:34158123
One-step peracetic acid pretreatment of hardwood and softwood biomass for platform chemicals production Kundu C, Samudrala SP, Kibria MA, Bhattacharya S Sci Rep 27-May-2021
PMCID:PMC8160206
doi:10.1038/s41598-021-90667-9
PMID:34045559
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
Efficacy of Minimum Application of Chlorfluazuron Baiting to Control Urban Subterranean Termite Populations of Coptotermes gestroi (Wasmann) (Blattodea: Rhinotermitidae) Wan Umar WA, Ab Majid AH Insects 25-Aug-2020
PMCID:PMC7564584
doi:10.3390/insects11090569
PMID:32854188

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
Benzylacetone 17355 Click to see CC(=O)CCC1=CC=CC=C1 148.20 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
4,6,6-Trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]bicyclo[3.1.1]hept-4-en-2-ol 56924154 Click to see CC1=C2CC(C2(C)C)CC1C3(CC4CC(=C3C)C4(C)C)C5C(C6CC(=C5C)C6(C)C)O 420.70 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
trans-Piperitol 85568 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1016/S0031-9422(00)84946-8
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> 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/10.1016/S0031-9422(00)84946-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1016/S0031-9422(00)84946-8
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,2S,19S,20S,21S)-7,8,9,12,13,14,20,27,28,29,32,33,34-tridecahydroxy-3,18,23,38,39-pentaoxaheptacyclo[19.17.1.02,19.05,10.011,16.025,30.031,36]nonatriaconta-5,7,9,11,13,15,25,27,29,31,33,35-dodecaene-4,17,24,37-tetrone 163033767 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O3)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/S0031-9422(00)85235-8
7,8,9,12,13,14,20,27,28,29,32,33,34-Tridecahydroxy-3,18,23,38,39-pentaoxaheptacyclo[19.17.1.02,19.05,10.011,16.025,30.031,36]nonatriaconta-5,7,9,11,13,15,25,27,29,31,33,35-dodecaene-4,17,24,37-tetrone 163033766 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O3)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/S0031-9422(00)85235-8

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