Eucalyptus coccifera - Unknown
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Internal ID UUID644039f4e32e3497252526
Scientific name Eucalyptus coccifera
Authority Hook.f.
First published in London J. Bot. 6: 477 (1847)

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Synonyms Top

Scientific name Authority First published in
Eucalyptus alpina R.Br. ex Maiden Rep. Meetings Australas. Assoc. Advancem. Sci. 9: 365. 1896 (1896)
Eucalyptus coccifera var. parviflora Benth. Fl. Austral. 3: 204 (1867)
Eucalyptus coccifera var. viridifolia Summerh. Bot. Mag. 160: t. 9511 (1934)
Eucalyptus daphnoides Miq. Ned. Kruidk. Arch. 4: 133 (1856)

Common names Top

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Language Common/alternative name
English tasmanian snow gum
Azerbaijani giləmeyvəli evkalipt
German trichterfrucht-eukalyptus
Upper Sorbian likopłodowy eukalyptowc
Russian Эвкалипт ягодоносный
Russian Эвкалипт ягодный
Chinese 浆果桉
Chinese 聚果桉

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000954670
USDA Plants EUCO27
Tropicos 100187621
INPN 97399
KEW urn:lsid:ipni.org:names:592806-1
The Plant List kew-72689
Open Tree Of Life 230868
NCBI Taxonomy 87665
NBN Atlas NHMSYS0000458615
IUCN Red List 133378615
IPNI 592806-1
iNaturalist 323285
GBIF 3176305
Freebase /m/047s4ld
EPPO EUCCC
EOL 301305
USDA GRIN 15877
Wikipedia Eucalyptus_coccifera
CMAUP NPO11300

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
Fifty years of change in the lower tree line in an arid coniferous forest in the Qilian Mountains, northwestern China Fang S, He Z, Zhao M PLoS One 12-Oct-2023
PMCID:PMC10569624
doi:10.1371/journal.pone.0292682
PMID:37824484
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
Phosphorus uptake and toxicity are delimited by mycorrhizal symbiosis in P-sensitive Eucalyptus marginata but not in P-tolerant Acacia celastrifolia Tibbett M, Daws MI, Ryan MH AoB Plants 21-Aug-2022
PMCID:PMC9521482
doi:10.1093/aobpla/plac037
PMID:36196393
Asymmetric Interaction Between Two Mycorrhizal Fungal Guilds and Consequences for the Establishment of Their Host Plants Fernández N, Knoblochová T, Kohout P, Janoušková M, Cajthaml T, Frouz J, Rydlová J Front Plant Sci 09-Jun-2022
PMCID:PMC9218742
doi:10.3389/fpls.2022.873204
PMID:35755655
Warming impacts potential germination of non-native plants on the Antarctic Peninsula Bokhorst S, Convey P, Casanova-Katny A, Aerts R Commun Biol 25-Mar-2021
PMCID:PMC7994377
doi:10.1038/s42003-021-01951-3
PMID:33767327
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
Lifespan and functionality of mycorrhizal fungal mycelium are uncoupled from host plant lifespan Pepe A, Giovannetti M, Sbrana C Sci Rep 06-Jul-2018
PMCID:PMC6035242
doi:10.1038/s41598-018-28354-5
PMID:29980700
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
Families of Diaporthales based on morphological and phylogenetic evidence Senanayake IC, Crous PW, Groenewald JZ, Maharachchikumbura SS, Jeewon R, Phillips AJ, Bhat JD, Perera RH, Li QR, Li WJ, Tangthirasunun N, Norphanphoun C, Karunarathna SC, Camporesi E, Manawasighe IS, Al-Sadi AM, Hyde KD Stud Mycol 01-Aug-2017
PMCID:PMC5603113
doi:10.1016/j.simyco.2017.07.003
PMID:28947840
Introducing the Consolidated Species Concept to resolve species in the Teratosphaeriaceae Quaedvlieg W, Binder M, Groenewald JZ, Summerell BA, Carnegie AJ, Burgess TI, Crous PW Persoonia 15-May-2014
PMCID:PMC4312929
doi:10.3767/003158514X681981
PMID:25737591
Sedges in the mist: A new species of Lepidosperma (Cyperaceae, Schoeneae) from the mountains of Tasmania Plunkett GT, Wilson KL, Bruhl JJ PhytoKeys 04-Nov-2013
PMCID:PMC3881413
doi:10.3897/phytokeys.28.5592
PMID:24399891
Fungal Planet description sheets: 107–127 Crous PW, Summerell BA, Shivas RG, Burgess TI, Decock CA, Dreyer LL, Granke LL, Guest DI, Hardy GE, Hausbeck MK, Hüberli D, Jung T, Koukol O, Lennox CL, Liew EC, Lombard L, McTaggart AR, Pryke JS, Roets F, Saude C, Shuttleworth LA, Stukely MJ, Vánky K, Webster BJ, Windstam ST, Groenewald JZ Persoonia 04-Jun-2012
PMCID:PMC3409410
doi:10.3767/003158512X652633
PMID:23105159
A re-appraisal of Harknessia (Diaporthales), and the introduction of Harknessiaceae fam. nov. Crous PW, Summerell BA, Shivas RG, Carnegie AJ, Groenewald JZ Persoonia 30-Mar-2012
PMCID:PMC3409415
doi:10.3767/003158512X639791
PMID:23105153
Myrtaceae, a cache of fungal biodiversity Cheewangkoon R, Groenewald JZ, Summerell BA, Hyde KD, To-anun C, Crous PW Persoonia 10-Sep-2009
PMCID:PMC2802731
doi:10.3767/003158509X474752
PMID:20198162
The road from Santa Rosalia: A faster tempo of evolution in tropical climates Wright S, Keeling J, Gillman L Proc Natl Acad Sci U S A 03-May-2006
PMCID:PMC1472511
doi:10.1073/pnas.0510383103
PMID:16672371

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
> Alkaloids and derivatives
7-Angelylretronecine 6440943 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)CO 237.29 unknown via CMAUP database
9-Angeloylretronecine 638872 Click to see CC=C(C)C(=O)OCC1=CCN2C1C(CC2)O 237.29 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
(R)-1-(5,8-Dihydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-4-methylpent-3-en-1-yl acetate 479501 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 330.30 unknown via CMAUP database
(S)-alpha-Methylbutyryl alkannin 637472 Click to see CCC(C)C(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 372.40 unknown via CMAUP database
[(1R)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl] 3-acetyloxy-3-methylbutanoate 69295815 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(C)(C)OC(=O)C)C 430.40 unknown via CMAUP database
[(1R)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-methylpent-3-enyl] 3,4-dimethylpent-3-enoate 15931504 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(=C(C)C)C)C 398.40 unknown via CMAUP database
Acetylalkannin 9967285 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 330.30 unknown via CMAUP database
Alkannin 72521 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown via CMAUP database
Alkannin beta,beta-dimethylacrylate 442720 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown via CMAUP database
Anhydroalkannin 101626182 Click to see CC(=CC=CC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 270.28 unknown via CMAUP database
beta-Hydroxyisovalerylshikonin 479502 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(C)(C)O)C 388.40 unknown via CMAUP database
beta,beta-Dimethylacrylshikonin 479499 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C=C(C)C)C 370.40 unknown via CMAUP database
Butanoic acid, 3-(acetyloxy)-3-methyl-, 1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester, (S)- 155245 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)CC(C)(C)OC(=O)C)C 430.40 unknown via CMAUP database
Deoxyshikonin 98914 Click to see CC(=CCCC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C 272.29 unknown via CMAUP database
Echinone 157629 Click to see CC(=CCC(C1=CC(=C2C(=O)C=CC(=O)C2=C1OC)O)OC(=O)C)C 344.40 unknown via CMAUP database
Isobutylalkannin 5318520 Click to see CC(C)C(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 358.40 unknown via CMAUP database
Isovalerylalkannin 5318685 Click to see CC(C)CC(=O)OC(CC=C(C)C)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 372.40 unknown via CMAUP database
Shikonin 479503 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Ethyl 9-(2,5-dihydroxyphenyl)nonanoate 91544169 Click to see CCOC(=O)CCCCCCCCC1=C(C=CC(=C1)O)O 294.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
(2R)-2-[(1R,2S)-3-[(1R)-1-carboxylato-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-1-(3,4-dihydroxyphenyl)-6,7-dihydroxy-1,2-dihydronaphthalene-2-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoate 5320234 Click to see C1=CC(=C(C=C1CC(C(=O)[O-])OC(=O)C2C(C3=CC(=C(C=C3C=C2C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)[O-])O)O)C5=CC(=C(C=C5)O)O)O)O 716.60 unknown via CMAUP database
Rabdosiin 471121 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2C(C3=CC(=C(C=C3C=C2C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)O)O)O)C5=CC(=C(C=C5)O)O)O)O 718.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Hopenone I 21603525 Click to see CC(C)C1=C2CCC3(C(C2(CC1)C)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones / Ubiquinones
5-[(E)-5-(furan-3-yl)-2-methylpent-2-enyl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 6505036 Click to see CC(=CCCC1=COC=C1)CC2=CC(=O)C(=C(C2=O)OC)OC 316.30 unknown via CMAUP database
Arnebifuranone 6438590 Click to see CC(=CCCC1=COC=C1)CC2=CC(=O)C(=C(C2=O)OC)OC 316.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosta-4,6,8(14),22-tetraen-3-one 6441416 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-ene-3,6-dione 5490007 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Alkyl aryl ethers
Arnebinol 5281558 Click to see CC1=CCC2=C(C=CC(=C2)OCC(=CCC1)C)O 244.33 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54691413 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)[O-] 193.18 unknown via CMAUP database
(R)-rosmarinate 25245604 Click to see C1=CC(=C(C=C1CC(C(=O)[O-])OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 359.30 unknown via CMAUP database
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
Octacosyl (E)-ferulate 5743442 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 586.90 unknown via CMAUP database
Octyl ferulate 15875260 Click to see CCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 306.40 unknown via CMAUP database
Tetracosyl ferulate 14238617 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 530.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(R)-de-O-methyllasioplodin 14562694 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)O)C(=O)O1 278.34 unknown via CMAUP database
De-O-Methyllasiodiplodin 14562695 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)O)C(=O)O1 278.34 unknown via CMAUP database

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