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Polylepis australis

Polylepis australis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403fa131069672581699
Scientific name Polylepis australis
Authority Bitter
First published in Bot. Jahrb. Syst. 45: 619 (1911)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polylepis racemosa var. albotomentella Kuntze Revis. Gen. Pl. 3(2): 77 (1898)
Polylepis australis var. glabra Bitter Bot. Jahrb. Syst. 45: 622 (1911)
Polylepis australis var. glabrescens Bitter Bot. Jahrb. Syst. 45: 623 (1911)
Polylepis australis var. subcalva Bitter Bot. Jahrb. Syst. 45: 623 (1911)
Polylepis australis var. oblanceolata Bitter Bot. Jahrb. Syst. 45: 623 (1911)
Polylepis australis var. latifoliolata Bitter Bot. Jahrb. Syst. 45: 624 (1911)
Polylepis australis var. fuscitomentella Bitter Bot. Jahrb. Syst. 45: 625 (1911)
Polylepis australis var. crenulata Bitter Bot. Jahrb. Syst. 45: 625 (1911)
Polylepis racemosa var. fuscotomentella Kuntze Revis. Gen. Pl. 3(2): 77 (1898)
Polylepis racemosa var. glabrescens Kuntze Revis. Gen. Pl. 3(2): 77 (1898)
Polylepis racemosa var. glabra Kuntze Revis. Gen. Pl. 3(2): 77 (1898)
Polylepis racemosa var. pubinervia Kuntze Revisio generum plantarum ; 1891 77 1898
Polylepis racemosa var. subresinosa Kuntze Revisio generum plantarum ; 1891 77 1898
Polylepis racemosa var. pubescens Kuntze Revisio generum plantarum ; 1891 77 1898
Polylepis australis var. tucumanica Bitter Repert. Spec. Nov. Regni Veg. 12: 478 (1913)
Polylepis racemosa f. albotomentella Kuntze Revis. Gen. Pl. 3(2): 77 (1898)

Common names Top

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Language Common/alternative name
Quechua kintu qiwuña

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001004595
Tropicos 27800727
KEW urn:lsid:ipni.org:names:206476-2
The Plant List rjp-3648
Open Tree Of Life 664137
NCBI Taxonomy 281887
IPNI 206476-2
iNaturalist 448484
GBIF 5370540
Freebase /m/02qhsc7
EPPO PPSAU
EOL 300983
Wikipedia Polylepis_australis

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
Co-Inoculation with Arbuscular Mycorrhizal Fungi and Dark Septate Endophytes under Drought Stress: Synergistic or Competitive Effects on Maize Growth, Photosynthesis, Root Hydraulic Properties and Aquaporins? Gong M, Bai N, Wang P, Su J, Chang Q, Zhang Q Plants (Basel) 09-Jul-2023
PMCID:PMC10383269
doi:10.3390/plants12142596
PMID:37514211
Repeated colonization of alpine habitats by Arabidopsis arenosa viewed through freezing resistance and ice management strategies Kaplenig D, Bertel C, Arc E, Villscheider R, Ralser M, Kolář F, Wos G, Hülber K, Kranner I, Neuner G Plant Biol (Stuttg) 11-Aug-2022
PMCID:PMC9804731
doi:10.1111/plb.13454
PMID:35833328
The complete chloroplast genome of Agrimonia pilosa Ledeb. isolated in Korea (Rosaceae): investigation of intraspecific variations on its chloroplast genomes Heo KI, Park J, Xi H, Min J Mitochondrial DNA B Resour 01-Jun-2020
PMCID:PMC7510681
doi:10.1080/23802359.2020.1772144
PMID:33367001
Land use alters arbuscular mycorrhizal fungal communities and their potential role in carbon sequestration on the Tibetan Plateau Xu M, Li X, Cai X, Li X, Christie P, Zhang J Sci Rep 08-Jun-2017
PMCID:PMC5465222
doi:10.1038/s41598-017-03248-0
PMID:28596609
Reintroducing Guanaco in the Upper Belt of Central Argentina: Using Population Viability Analysis to Evaluate Extinction Risk and Management Priorities Barri FR PLoS One 14-Oct-2016
PMCID:PMC5065184
doi:10.1371/journal.pone.0164806
PMID:27741302
Unrestricted quality of seeds in European broad-leaved tree species growing at the cold boundary of their distribution Kollas C, Vitasse Y, Randin CF, Hoch G, Körner C Ann Bot 07-Dec-2011
PMCID:PMC3268544
doi:10.1093/aob/mcr299
PMID:22156401
Variation of Pollinator Assemblages and Pollen Limitation in a Locally Specialized System: The Oil-producing Nierembergia linariifolia (Solanaceae) Cosacov A, Nattero J, Cocucci AA Ann Bot 02-Sep-2008
PMCID:PMC2712377
doi:10.1093/aob/mcn154
PMID:18765440
Two Measurement Methods of Leaf Dry Matter Content Produce Similar Results in a Broad Range of Species Vaieretti MV, Díaz S, Vile D, Garnier E Ann Bot 12-Mar-2007
PMCID:PMC2802913
doi:10.1093/aob/mcm022
PMID:17353207
Oleanolic and ursolic acid derivatives from Polylepis australis Marina E.P De Lampasona, Cesar A.N Catalán, Thomas E Gedris, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00408-7

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 / Naphthalenes / Naphthols and derivatives
Nepodin 100780 Click to see CC1=CC2=C(C(=CC=C2)O)C(=C1C(=O)C)O 216.23 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Maslinic acid methyl ester 609113 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
methyl (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicene-4a-carboxylate 10552895 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 484.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
methyl (4aS,6aR,6aS,6bR,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 3082208 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
methyl (4aS,6aR,6aS,6bR,8aR,10S,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-4a-carboxylate 21723770 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 484.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
methyl (4aS,6aR,6bS,8aR,10S,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,14b-dodecahydropicene-4a-carboxylate 100952799 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 468.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl 10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,14b-dodecahydropicene-4a-carboxylate 162961390 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 468.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
methyl 10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-4a-carboxylate 14563358 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 484.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl 2,3-dihydroxyurs-12-en-28-oate 621722 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl 3-acetoxy-3-dehydroxyursolate 11443665 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)OC 512.80 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl 3-hydroxy-11-oxours-12-en-28-oate 629023 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 484.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl acuminate 14314584 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC 502.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl corosolate 14109751 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl maslinate 13653327 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Methyl oleanolate acetate 10255859 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 512.80 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Olean-12-en-28-oic acid, 3beta-hydroxy-, methyl ester, acetate 609115 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 512.80 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, methyl ester, (2alpha,3beta)- 601648 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC 502.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7
Ursolic acid methyl ester 89432794 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(98)00408-7

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