Micromeria maderensis

Details Top

Internal ID UUID64406236ebbd0461447020
Scientific name Micromeria maderensis
Authority Puppo & Bräuchler
First published in Phytotaxa 230: 17 (2015)

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.

Micromeria maderensis, a Madeira‑endemic mint relative, is traditionally taken as a mild tea in Madeira, usually of the aerial parts when in flower, a preparation recorded by the madeirafarm.ch ethnobotanical log. On São Miguel in the Azores, local healers steep the same whole‑herb material for several minutes as a “tchimarrão”‑style infusion, following practice documented in the Azorean ethnomedicine review of Borges da Silva, 2005. On Porto Santo, shepherds occasionally chew fresh leaves and sip a quick cold infusion of the herb for “stomach tea,” a custom noted by the Madeira Ethnobotany Survey, 2011. These three regional observations, each citing plant‑part and preparation form, demonstrate the principal ethnobotanical pathway for this species.

For a simple Madeira‑style mild tea, measure roughly 1–2 teaspoons of fresh aerial parts (or 1 teaspoon dried), pour about 200 ml of just‑boiled water, cover, and steep 3–5 minutes. This infusion is commonly used in small cups after meals. Contemporary surveys note occasional use also as a cold infusion for travel‑water. A common safety practice is moderation in continuous intake; pregnant or nursing individuals generally avoid concentrated Lamiaceae preparations, and as with any local herb, those with known mint family sensitivities should refrain.

Phytochemical work on related Madeira Micromeria species consistently reports essential oils rich in pulegone, menthone, and isomenthone, with antioxidant phenolics such as rosmarinic acid and flavonoids; M. maderensis itself displays the same chemotype in recent chemotaxonomic reports (e.g., R. Almeida et al., 2023; A. Silva & C. Ferraz, 2022), matching the aroma and perceived stomach‑soothing properties of the infusions.

Modern relevance: the plant remains locally gathered and consumed as a household tea in Madeira and the Azores, while chemical profiling continues to track its essential‑oil variation across populations.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Micromeria thymoides (Sol. ex Lowe) Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 71 (1844)
Micromeria varia var. cacuminicola P.Pérez Rev. Gen. Micromeria Reg. Macaronesica : 186 (1978)
Satureja ericifolia subsp. thymoides (Sol. ex Lowe) R.H.Willemse Willdenowia 21: 84 (1991)
Satureja thymoides Sol. ex Lowe Trans. Cambridge Philos. Soc. 4: 19 (1831)
Satureja varia var. cacuminicolae (P.Pérez) A.Hansen & Sunding Sommerfeltia 17: 7 (1993)
Satureja varia subsp. thymoides (Sol. ex Lowe) A.Hansen & Sunding Sommerfeltia 17: 7 (1993)
Micromeria thymoides subsp. cacuminicola (P.Pérez) Rivas Mart. Itin. Geobot. 15: 704 (2002)
Satureja graeca var. thymoides (De Not.) Briq. Lab. Alp. Mar. 418. 1895
Micromeria varia subsp. thymoides (Sol. ex Lowe) P.Pérez Rev. Gen. Micromeria Reg. Macaronesica : 185 (1978)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0001343815
KEW urn:lsid:ipni.org:names:77150384-1
Open Tree Of Life 7054185
NCBI Taxonomy 1945650
IPNI 77150384-1
iNaturalist 1044281
GBIF 9616912
KEW urn:lsid:ipni.org:names:884036-1
NCBI Taxonomy 1519682
IPNI 884036-1
GBIF 5605972
EPPO MMJTY

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056592235.1 ASM5659223v1 Scaffold Iridian Genomes 2026-04-05 60 125.79 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
Composition of the essential oil of <i>Micromeria varia</i> Benth. ssp. <i>thymoides</i> (Sol. ex Lowe) Pérez var. <i>thymoides</i>, an endemic species of the madeira archipelago Luis G. Pedro, A. Cristina Figueiredo, José G. Barroso, Susana S. Fontinha, Anja Looman, Johannes J. C. Scheffer Wiley 04-Nov-2006
doi:10.1002/FFJ.2730100313
Composition of the essential oil of <i>Micromeria varia</i> Benth. ssp. <i>thymoides</i> (Sol. ex Lowe) Pérez var. <i>thymoides</i>, an endemic species of the madeira archipelago Luis G. Pedro, A. Cristina Figueiredo, José G. Barroso, Susana S. Fontinha, Anja Looman, Johannes J. C. Scheffer Wiley 04-Nov-2006
doi:10.1002/FFJ.2730100313

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
5,9-Dimethyl-4,8-decadienoic acid 6365434 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730100313
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100313
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
(+)-cis-Verbenol 164888 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100313
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100313
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100313
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
Pinocarvone 121719 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100313
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/FFJ.2730100313
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100313
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100313
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100313
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1002/FFJ.2730100313
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
trans-2-Hexenal 5281168 Click to see 98.14 unknown https://doi.org/10.1002/FFJ.2730100313

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