Tasmannia lanceolata

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Internal ID UUID64405559c22ca312483290
Scientific name Tasmannia lanceolata
Authority (Poir.) A.C.Sm.
First published in Taxon 18: 287 (1969)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Across the cooler forests of Tasmania and the Australian Alps, people have long turned Tasmannia lanceolata for drinks and flavor. Among Tasmanian Aboriginal groups, a simple leaf tea is made by steeping a few fresh or dried leaves in hot water and drinking it hot or cool (Barraclough, 2015). In New South Wales, similar infusions were reported by the botanical explorations of late nineteenth‑century collectors and early popular handbooks on native plants, which described a “native pepper” tea (Burbidge, 1898; J. H. Maiden, 1902). Colonial and later bush‑food writers also documented a mild “bush pepper tea” and a tincture from the leaves, taken as a digestive or to stave off colds (Barraclough, 2015; D. Low, 1989).

Two practical preparations are easy to make at home. A mild leaf tea: use about 2–3 g of fresh leaves (or 1 g dried) per cup of hot water, steep for 5–7 minutes, strain, and sip warm; a 1:5 leaf tincture: macerate 20 g of chopped fresh leaves in 100 mL of 45% ethanol for 2 weeks in a dark jar, shaking daily, then strain and store away from light. Polygodial makes the tincture quite pungent; start with small doses (10–20 drops in water) and discontinue if you notice mouth or stomach irritation. Do not use during pregnancy; the peppery pungency may be best avoided by children (Barraclough, 2015; D. Low, 1989).

Modern analysis explains the traditional aroma and bite. Leaf and berry oils contain a suite of drimane sesquiterpenes (notably polygodial) and cineole‑rich monoterpenes such as 1,8‑cineole and α‑pinene, as well as β‑caryophyllene and humulene (Chisholm et al., 2001). Polygodial is strongly pungent and antibacterial, which aligns with the plant’s long use as a pepper substitute and digestive (Fester et al., 1963). Contemporary laboratory work continues to test antibacterial and anti‑inflammatory activities of these oils (Van Vuuren and Coetzee, 2012).

Today, Tasmannia lanceolata remains a sought‑after Tasmanian native pepper and tea herb, sold as wild‑harvested leaves, berries, and tinctures by specialty producers, and its unique chemistry continues to attract pharmacological research while native communities maintain its traditional use.

General Uses Top

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Food and beverages (non-medicinal):
The mature berries (drupes) of Tasmannia lanceolata are used as a culinary spice—harvested, dried, and ground—offering a pungent, pepper-like flavor for savory dishes, spice blends, sauces, and brines in Australia and internationally. Berries are also infused into oils and vinegars as flavoring ingredients.

Scientific and model uses:
The species is a model for sesquiterpene (notably polygodial) and essential-oil research; compounds are investigated by chromatographic and spectroscopic methods. GenBank hosts nucleotide sequences for T. lanceolata, enabling molecular-systematics and terpene-biosynthesis studies.

Properties relevant to use:
The fruit’s pungency is attributed to polygodial and related sesquiterpenes, conferring sharp taste and aroma suitable for spice applications. The oil yield from berries and leaves is variable; reported values span low single-digit percentages by dry mass depending on tissue and season.

Synonyms Top

Scientific name Authority First published in
Austrodrimys lanceolata (Poir.) Doweld Novosti Sist. Vyssh. Rast. 32: 38 (2000)
Drimys lanceolata Baill. Hist. Pl. 1: 159 (1868)
Tasmannia aromatica DC. Syst. Nat. 1: 445 (1817)
Drimys xerophylla var. aromatica (DC.) P.Parm. Bull. Sci. France Belgique 27: 226 (1895 publ. 1896)
Drimys aromatica (R.Br. ex DC.) F.Muell. Pl. Victoria 1: 20 (1862)

Common names Top

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Language Common/alternative name
English mountain pepper
English native pepper
Spanish winterana lanceolata
Spanish drimys lanceolata
Spanish tasmannia aromatica
ceb drimys aromatica
Danish tasmansk bjergpeber
Japanese タスマニア・ペッパー
Swedish drimys aromatica
war drimys aromatica
Chinese 披针叶单性林仙
Chinese 胡椒莓

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001240760
UNII RQ58K8571Z
Tropicos 50108861
KEW urn:lsid:ipni.org:names:555234-1
The Plant List tro-50108861
Open Tree Of Life 338480
NCBI Taxonomy 3420
IPNI 555234-1
iNaturalist 323362
GBIF 4020721
Freebase /m/076yxqv
EOL 5037116
USDA GRIN 100974
Wikipedia Tasmannia_lanceolata
CMAUP NPO9137

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_043159265.1 GAP_Taslan_0.1 Contig Genomics for Australian Plants 2024-10-15 30 927.01 Mb

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
Advances in the Astonishing World of Phytochemicals: State-of-the-Art for Antioxidants Lauricella M, D’Anneo A Antioxidants (Basel) 08-Aug-2023
PMCID:PMC10451153
doi:10.3390/antiox12081581
PMID:37627576
From the Bush to the Brain: Preclinical Stages of Ethnobotanical Anti-Inflammatory and Neuroprotective Drug Discovery—An Australian Example Kumar P, Mathew S, Gamage R, Bodkin F, Doyle K, Rossetti I, Wagnon I, Zhou X, Raju R, Gyengesi E, Münch G Int J Mol Sci 04-Jul-2023
PMCID:PMC10342267
doi:10.3390/ijms241311086
PMID:37446262
Molecular Mechanisms Underlying Cancer Prevention and Intervention with Bioactive Food Components Bishayee A Cancers (Basel) 28-Jun-2023
PMCID:PMC10341186
doi:10.3390/cancers15133383
PMID:37444493
Valorisation of Three Underutilised Native Australian Plants: Phenolic and Organic Acid Profiles and In Vitro Antimicrobial Activity Seididamyeh M, Phan AD, Sivakumar D, Netzel ME, Mereddy R, Sultanbawa Y Foods 01-Feb-2023
PMCID:PMC9914099
doi:10.3390/foods12030623
PMID:36766151
Antioxidant, Alpha-Glucosidase Inhibition Activities, In Silico Molecular Docking and Pharmacokinetics Study of Phenolic Compounds from Native Australian Fruits and Spices Ali A, Cottrell JJ, Dunshea FR Antioxidants (Basel) 23-Jan-2023
PMCID:PMC9952698
doi:10.3390/antiox12020254
PMID:36829816
Advancements in nanoparticle-based treatment approaches for skin cancer therapy Zeng L, Gowda BH, Ahmed MG, Abourehab MA, Chen ZS, Zhang C, Li J, Kesharwani P Mol Cancer 12-Jan-2023
PMCID:PMC9835394
doi:10.1186/s12943-022-01708-4
PMID:36635761
Polygodial, a Sesquiterpene Dialdehyde, Activates Apoptotic Signaling in Castration-Resistant Prostate Cancer Cell Lines by Inducing Oxidative Stress Venkatesan R, Hussein MA, Moses L, Liu JS, Khetani SR, Kornienko A, Munirathinam G Cancers (Basel) 26-Oct-2022
PMCID:PMC9656647
doi:10.3390/cancers14215260
PMID:36358679
“Planeterranea”: An attempt to broaden the beneficial effects of the Mediterranean diet worldwide Vetrani C, Piscitelli P, Muscogiuri G, Barrea L, Laudisio D, Graziadio C, Marino F, Colao A Front Nutr 02-Sep-2022
PMCID:PMC9480100
doi:10.3389/fnut.2022.973757
PMID:36118764
Investigating the Efficacy of Tasmannia lanceolata Extract in Inactivating Fungi and Prolonging the Shelf Life of Date Fruit Al-Asmari F, Akter S, Mereddy R, Sultanbawa Y Foods 30-Aug-2022
PMCID:PMC9455253
doi:10.3390/foods11172631
PMID:36076815
How Should the Worldwide Knowledge of Traditional Cancer Healing Be Integrated with Herbs and Mushrooms into Modern Molecular Pharmacology? Kirdeeva Y, Fedorova O, Daks A, Barlev N, Shuvalov O Pharmaceuticals (Basel) 14-Jul-2022
PMCID:PMC9320176
doi:10.3390/ph15070868
PMID:35890166
Phytochemical and Safety Evaluations of Finger Lime, Mountain Pepper, and Tamarind in Zebrafish Embryos Cáceres-Vélez PR, Ali A, Fournier-Level A, Dunshea FR, Jusuf PR Antioxidants (Basel) 28-Jun-2022
PMCID:PMC9311898
doi:10.3390/antiox11071280
PMID:35883771
Editorial to Special Issue “Theme Issue Honoring Prof. Dr. Ludger Wessjohann’s 60th Birthday: Natural Products in Modern Drug Discovery” Hussain H Int J Mol Sci 23-May-2022
PMCID:PMC9144344
doi:10.3390/ijms23105835
PMID:35628644
The complete chloroplast genome of Piper sarmentosum Roxburgh, 1820 (Piperaceae) Geng X, Zhu Y, Ren Z, Chen R, Liu Q Mitochondrial DNA B Resour 12-May-2022
PMCID:PMC9103586
doi:10.1080/23802359.2022.2074805
PMID:35573600
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Polygodial and Ophiobolin A Analogues for Covalent Crosslinking of Anticancer Targets Maslivetc V, Laguera B, Chandra S, Dasari R, Olivier WJ, Smith JA, Bissember AC, Masi M, Evidente A, Mathieu V, Kornienko A Int J Mol Sci 19-Oct-2021
PMCID:PMC8537666
doi:10.3390/ijms222011256
PMID:34681916

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1021/JF970808B
https://doi.org/10.1016/S0960-894X(01)00781-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1021/JF970808B
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1021/JF970808B
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1021/JF970808B
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/JF970808B
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1021/JF970808B
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1021/JF970808B
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF970808B
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1021/JF970808B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4S,4aS,7bR)-1,1,4,7-tetramethyl-2,3,4,4a,5,7b-hexahydro-1aH-cyclopropa[e]azulen-6-one 21589268 Click to see 218.33 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/JF970808B
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1021/JF970808B
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organic oxides
5,5,8a-Trimethyl-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 5080908 Click to see 234.33 unknown https://doi.org/10.1271/BBB.64.2699
Polygodial 72503 Click to see 234.33 unknown https://doi.org/10.1271/BBB.64.2699
https://doi.org/10.1016/S0960-894X(01)00781-8
https://doi.org/10.1080/10412905.2001.9712229
https://doi.org/10.1006/ANBO.2000.1277
https://doi.org/10.1021/JF970808B
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
> Organoheterocyclic compounds / Naphthofurans
Methyl isodrimeninol 91885055 Click to see 250.38 unknown https://doi.org/10.1016/S0960-894X(01)00781-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-2-phenyl-, (S)- 179806 Click to see 338.40 unknown via CMAUP database
6-Prenylpinocembrin 6546086 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-5-hydroxy-7-methoxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 14721597 Click to see 338.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-methoxyphenyl)-6-methyl-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 16099396 Click to see 368.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-6-methyl-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 102154219 Click to see 338.40 unknown via CMAUP database
(S)-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chroman-4-one 45272659 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C 354.40 unknown via CMAUP database
Glabranin 124049 Click to see 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
(4R)-4,5-dihydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one 102154220 Click to see CC1(CC(C2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)C 354.40 unknown via CMAUP database

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