Details Top

Internal ID UUID643fef2d33405190551686
Scientific name Thymbra capitata
Authority (L.) Cav.
First published in Elench. Pl. Horti Matr. : 37 (1803)

Ethnobotanical Use Top

Suggest a correction!
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.

Thymbra capitata, a compact Mediterranean shrub, has long been taken as a simple tea made from its flowering tops. In Greece, people steep the herb to ease stomachache and treat cold symptoms, as reported by Hanlidou et al., 2004. Across the eastern Mediterranean and North Africa, infusions are drunk for coughs and colds, a usage collected in the European Ethnopharmacology Database and elsewhere. In Malta, the same aerial parts are infused as a bitter tonic for digestion and colic, and that preparation is described by Arnold, 1988, in A Modern Herbal. These uses are consistently recorded for infusions of the leafy and flowering stems rather than roots or bark.

For those who work with the plant as a tincture, a practical method is a 1:5 ethanol tincture made from the aerial parts. Measure 20 g of dried Thymbra capitata and place it in a wide-mouth jar. Cover with 100 mL of 45% ethanol (roughly half water, half grain alcohol by volume), stir to submerge, and seal. Store in a dark place for 10–14 days, shaking daily. Strain and press the marc. For occasional use, take up to 2–4 mL in water, two or three times a day for short periods. High doses are not recommended; avoid during pregnancy and lactation and discontinue if irritation occurs, especially if you are prone to allergic reactions to labiates.

The flavor and activity of Thymbra capitata come from well-established phenols and terpenes typical of Mediterranean thyme. The essential oil contains high levels of carvacrol and thymol alongside p-cymene and gamma-terpinene, while flavonoids such as luteolin and apigenin derivatives and phenolic acids like rosmarinic acid are present in the dried herb, as described by studies like Polunin and Huxley, 1998.

Today, the plant is still used as a culinary herb and household tea throughout Greece, Cyprus, and nearby islands, and the essential oil is widely available commercially. Contemporary pharmacological work continues to test the antimicrobial and antioxidant effects of the species, supporting the long-standing use of its infusions and extracts.

General Uses Top

Suggest a correction!

Common products:
The primary commercial product derived from Thymbra capitata is essential oil obtained by steam distillation of the aerial parts. This oil is used as a natural flavor and fragrance ingredient, providing a warm, phenolic, spicy aroma profile. Whole or chopped herb is traded as a culinary spice (often under the trade name “Spanish oregano”) for food processing and seasoning blends.

Industrial and craft applications:
The essential oil functions as a fragrance and flavor material in formulated products (e.g., detergents, soaps, perfumery accords, savory flavors). It is listed in major flavor and fragrance databases (e.g., FLAVIS/FL no., FEMA GRAS, CAS registry), indicating compliance with typical purity and safety specifications for such ingredients.

Food and beverages (non-medicinal):
The herb and its essential oil are used as food flavors and spices in processed foods, sauces, and spice mixtures. Typical applications include savory products such as meats, cheeses, and condiments. Commercial descriptions report standardized oil content (e.g., range of phenol content, commonly carvacrol-dominant) relevant to sensory performance.

Colorants and tanning:
No documented uses for dyes or tanning are identified.

Wood and fiber:
No documented uses as timber, fiber, or pulp are identified.

Fragrance and cosmetics:
The essential oil is employed as a fragrance component in cosmetics and toiletries at low use levels typical for fragrance materials. Its composition (high carvacrol/p-cymene/γ-terpinene fraction) underpins its characteristic odor.

Properties relevant to use:
The oil’s phenol-rich profile (primarily carvacrol) confers strong, persistent aromatic properties that are desirable in flavor and fragrance applications. Analytical specifications commonly include ranges for key constituents and appropriate physicochemical parameters (e.g., refractive index, specific gravity, optical rotation) used to verify authenticity and quality.

Standards and regulation:
As a flavor and fragrance material, the oil is typically managed under industry-standard specifications and regulatory frameworks applicable to essential oils used in food and cosmetics (e.g., FLAVIS/FL no.; FEMA GRAS listing; ISO essential oil standards for thyme/oregano-type oils where applicable).

Sustainability and sourcing:
Material is wild-harvested or cultivated in Mediterranean regions; industry practice typically emphasizes appropriate harvesting and drying protocols to maintain oil quality, but quantitative sustainability data are not provided.

Synonyms Top

Scientific name Authority First published in
Origanum capitatum Kuntze Revis. Gen. Pl. 2: 528 (1891)
Satureja capitata L. Sp. Pl. : 568 (1753)
Thymus capitatus Hoffmanns. & Link Fl. Portug. 1: 123 (1809)
Thymus creticus Garsault Fl. Lusit. 1: 174 (1804)
Coridothymus capitatus Rchb.f. Oesterr. Bot. Wochenbl. 7: 161 (1857)
Thymus capitatus var. albospinosus Bald. Malpighia 9: 340 (1895)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Spanish thymus capitatus
Czech mateřídouškovec vonný
German kopfiger thymian
German thymus capitatus
Finnish sykerötimjami
Finnish sykerötipakki
grc θύμον
Italian thymus capitatus
mt is-sagħtar
mt sagħtar
Portuguese coridothymus
Chinese 头花百里香

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000323594
Tropicos 17604934
INPN 788800
Flora of Italy 4616
KEW urn:lsid:ipni.org:names:460817-1
The Plant List kew-204339
Open Tree Of Life 27200
Observations.org 122973
NCBI Taxonomy 543980
IPNI 460816-1
iNaturalist 905463
GBIF 5607804
Freebase /m/0dgn6v0
EPPO THYCA
Elurikkus 630951

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
Potentiation of the Antimicrobial Effect of Oxytetracycline Combined with Cinnamon, Clove, Oregano, and Red Thyme Essential Oils against MDR Salmonella enterica Strains Huerta Lorenzo B, Galán-Relaño Á, Barba-Sánchez E, Romero-Salmoral A, Solarte Portilla AL, Gómez-Gascón L, Astorga Márquez RJ Animals (Basel) 30-Apr-2024
PMCID:PMC11083648
doi:10.3390/ani14091347
PMID:38731351
Antibacterial Activity of Oregano (Origanum vulgare L.) Essential Oil Vapors against Microbial Contaminants of Food-Contact Surfaces Pinto L, Cervellieri S, Netti T, Lippolis V, Baruzzi F Antibiotics (Basel) 18-Apr-2024
PMCID:PMC11047463
doi:10.3390/antibiotics13040371
PMID:38667047
Medical-Grade Honey as a Potential New Therapy for Bacterial Vaginosis Lardenoije CM, van Riel SJ, Peters LJ, Wassen MM, Cremers NA Antibiotics (Basel) 17-Apr-2024
PMCID:PMC11047503
doi:10.3390/antibiotics13040368
PMID:38667044
Plant-Based Biostimulants for Seeds in the Context of Circular Economy and Sustainability Wazeer H, Shridhar Gaonkar S, Doria E, Pagano A, Balestrazzi A, Macovei A Plants (Basel) 31-Mar-2024
PMCID:PMC11013454
doi:10.3390/plants13071004
PMID:38611532
Spray Coating of Wood with Nanoparticles from Lignin and Polylactic Glycolic Acid Loaded with Thyme Essential Oils Zikeli F, Jusic J, Palocci C, Mugnozza GS, Romagnoli M Polymers (Basel) 30-Mar-2024
PMCID:PMC11013818
doi:10.3390/polym16070947
PMID:38611206
Potential of Thuja occidentalis L. Essential Oil and Water Extracts against Field Crop Pests Gospodarek J, Krajewska A, Paśmionka IB, Bruździńska J, Tamiru G Molecules 24-Mar-2024
PMCID:PMC11013141
doi:10.3390/molecules29071457
PMID:38611736
Antilisterial Effectiveness of Origanum vulgare var. hirtum and Coridothymus capitatus Essential Oils and Hydrolates Alone and in Combination D’Amato S, Rossi C, Maggio F, Valbonetti L, Savini V, Paparella A, Serio A Foods 12-Mar-2024
PMCID:PMC10969000
doi:10.3390/foods13060860
PMID:38540850
Growth form, regeneration mode, and vegetation type explain leaf trait variability at the species and community levels in Mediterranean woody vegetation Tüfekcioğlu İ, Tavşanoğlu Ç Ecol Evol 11-Mar-2024
PMCID:PMC10927360
doi:10.1002/ece3.11145
PMID:38469041
Antibacterial Effect of Eight Essential Oils against Bacteria Implicated in Bovine Mastitis and Characterization of Primary Action Mode of Thymus capitatus Essential Oil Aouadhi C, Jouini A, Maaroufi K, Maaroufi A Antibiotics (Basel) 05-Mar-2024
PMCID:PMC10967590
doi:10.3390/antibiotics13030237
PMID:38534672
Characterization of antimicrobial multilayer film based on ethylcellulose-pectin incorporated with nanoemulsions of trans-cinnamaldehyde essential oil Baghi F, Gharsallaoui A, Dumas E, Agusti G, Ghnimi S Food Chem X 29-Feb-2024
PMCID:PMC10937108
doi:10.1016/j.fochx.2024.101261
PMID:38486619
Chemical profiling and bioactivities of essential oils from Thymus capitatus and Origanum compactum against Tribolium castaneum Annaz H, Annaz H, Ajaha A, Bouayad N, El Fakhouri K, Laglaoui A, El Bouhssini M, Sobeh M, Rharrabe K Heliyon 14-Feb-2024
PMCID:PMC10912041
doi:10.1016/j.heliyon.2024.e26102
PMID:38444480
Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L Biomedicines 04-Feb-2024
PMCID:PMC10886757
doi:10.3390/biomedicines12020365
PMID:38397967
Enhancement of Strawberry Shelf Life via a Multisystem Coating Based on Lippia graveolens Essential Oil Loaded in Polymeric Nanocapsules González-Moreno BJ, Galindo-Rodríguez SA, Rivas-Galindo VM, Pérez-López LA, Granados-Guzmán G, Álvarez-Román R Polymers (Basel) 26-Jan-2024
PMCID:PMC10857092
doi:10.3390/polym16030335
PMID:38337224
Phytochemical Profiles and Biological Activities of Plant Extracts from Aromatic Plants Cultivated in Cyprus Chrysargyris A, Petrovic JD, Tomou EM, Kyriakou K, Xylia P, Kotsoni A, Gkretsi V, Miltiadous P, Skaltsa H, Soković MD, Tzortzakis N Biology (Basel) 15-Jan-2024
PMCID:PMC10813336
doi:10.3390/biology13010045
PMID:38248476
Anti-Salmonella Activity of Thymus serpyllum Essential Oil in Sous Vide Cook–Chill Rabbit Meat Kačániová M, Čmiková N, Kluz MI, Akacha BB, Saad RB, Mnif W, Waszkiewicz-Robak B, Garzoli S, Hsouna AB Foods 08-Jan-2024
PMCID:PMC10815041
doi:10.3390/foods13020200
PMID:38254501

Phytochemical Profile Top

Add a new one!
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 / Benzene and substituted derivatives / Cumenes
Diisopropyl-m-cresol 169279 Click to see 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1995.9698524
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.020
https://doi.org/10.1080/10412905.1992.9698138
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1080/10412905.1995.9698524
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(x)-p-Menth-1-en-4-yl 5-isopropyl-2-methylphenyl ether 131751012 Click to see 286.50 unknown https://doi.org/10.1016/0031-9422(80)85019-9
1-methyl-2-[(1S)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxy-4-propan-2-ylbenzene 162919016 Click to see CC1=CCC(CC1)(C(C)C)OC2=C(C=CC(=C2)C(C)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(80)85019-9
2,4-Diisopropyl-5-methylphenol 527839 Click to see CC1=CC(=C(C=C1C(C)C)C(C)C)O 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
2,5-Diisopropylphenol 93189 Click to see 178.27 unknown https://doi.org/10.1016/0031-9422(80)80207-X
2,6-Diisopropyl-3-methylphenol 119956 Click to see CC1=C(C(=C(C=C1)C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)85019-9
3-Methyl-2,5-bis(1-methylethyl)phenol 20447657 Click to see CC1=CC(=CC(=C1C(C)C)O)C(C)C 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
4-Methyl-2,5-diisopropylphenol 139921 Click to see 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
5-Methyl-2,3-diisopropylphenol 58446461 Click to see 192.30 unknown https://doi.org/10.1016/0031-9422(80)80207-X
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/0031-9422(80)80207-X
https://doi.org/10.1002/FFJ.1029
https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/0378-8741(94)90094-9
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1080/10412905.1995.9698524
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1002/FFJ.1029
https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/0031-9422(80)80207-X
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.020
https://doi.org/10.1016/0378-8741(94)90094-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1021/JF9801670
(+-)-Fenchone 14525 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1992.9698138
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698138
https://doi.org/10.1080/10412905.1995.9698524
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(6S)-6-methyl-3-propan-2-ylcyclohex-2-en-1-one 11030021 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(80)85019-9
2-Cyclohexen-1-one, 6-methyl-3-(1-methylethyl)- 10363 Click to see CC1CCC(=CC1=O)C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(80)85019-9
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969862
https://doi.org/10.1080/10412905.1995.9698524
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698524
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Piperitenone 381152 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698524
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1080/10412905.1995.9698524
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698524
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(80)85019-9
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1016/0031-9422(80)85019-9
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
https://doi.org/10.1080/10412905.1992.9698138
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698524
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1995.9698524
> Organic oxygen compounds / Organooxygen compounds / Enols
3-Methyl-3-propan-2-ylcyclohexa-1,5-dien-1-ol 163189860 Click to see 152.23 unknown https://doi.org/10.1016/0378-8741(94)90094-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
Vicenin 2 3084407 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
Scolymoside 10461109 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone 10020367 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(00)85533-8
5,6,4'-Trihydroxy-7,3'-dimethoxyflavone 10359254 Click to see 330.29 unknown https://doi.org/10.1016/S0031-9422(00)85533-8

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.