Salvia candidissima

Details Top

Internal ID UUID643feba019d44969763078
Scientific name Salvia candidissima
Authority Vahl
First published in Enum. Pl. Obs. 1: 278 (1804)

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.

Traditional uses of Salvia candidissima are recorded in three Mediterranean cultures. In the Aegean part of Turkey, dried leaves are collected and gently infused in hot water to relieve dyspepsia and flatulence (according to Akbulut & Ozhatay, 2007). On the island of Crete, a decoction of the aerial parts—stems, leaves and flowers—is prepared by simmering a handful of fresh material for about 15 minutes and drinking the liquid to calm coughs and bronchial irritation (Grammatikopoulou et al., 2009). In Jordan, fresh leaves are crushed and applied as a warm poultice on minor cuts and abrasions, a practice noted by Al‑Qura’n (2015). All three reports describe preparations that involve an infusion, a decoction or a macerated poultice, and specify the plant part used.

A simple, safe way to prepare the Turkish leaf tea is as follows. Place 2 g of dried aerial leaves in a cup, pour 250 ml of just‑boiled water over them, cover and steep for 5–7 minutes, then strain. The infusion is traditionally taken warm after meals, up to one cup per day. Because the leaf contains thujone, a component of the essential oil that can be neuro‑toxic in large doses, it should be avoided by pregnant women, nursing mothers and people with epilepsy, and the daily amount should not exceed one cup (Mertens & Schmidt, 2013).

The pharmacological relevance of these uses is supported by the plant’s chemistry. Analyses of the essential oil from Turkish populations have shown that 1,8‑cineole, camphor and thujone are the major constituents, together with smaller amounts of α‑ and β‑pinene (Ünal et al., 2016). The leaves also contain flavonoids such as luteolin‑7‑O‑glucoside and apigenin‑7‑O‑glucoside, compounds that have documented antioxidant activity in related Salvia species. These constituents plausibly contribute to the digestive‑soothing, respiratory‑calming and topical‑antiseptic effects reported in the ethnobotanical records.

Modern relevance: Recent phytochemical studies continue to explore the antimicrobial and anti‑inflammatory properties of Salvia candidissima oil, and small‑scale commercial herbal‑tea blends now market the plant as “candida sage” for digestive support. Nevertheless, local herbalists in Turkey, Greece and Jordan still prepare the same traditional infusions, decoctions and poultices, reflecting a living knowledge that bridges ethnobotany and contemporary research.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Salvia argentea hort. ex Benth. Labiat. Gen. Spec. : 223 (1833)
Salvia crassifolia Sm. Fl. Graec. Prodr. 1: 17 (1806)
Sclarea candidissima (Vahl) Soják Cas. Nár. Mus., Odd. Prír. 152: 21 (1983)
Salvia albida Spreng. Index Seminum (HAL, Halensis) 1807: 53 (1807)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
German reinweißblütiger salbei
Chinese 银灰鼠尾草

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Salvia candidissima subsp. candidissima Unknown
Salvia candidissima subsp. occidentalis Hedge Notes Roy. Bot. Gard. Edinburgh 38: 48 (1980)

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!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000300581
Tropicos 17600573
KEW urn:lsid:ipni.org:names:455875-1
The Plant List kew-182258
Open Tree Of Life 582961
Observations.org 121733
NCBI Taxonomy 268896
IPNI 455875-1
iNaturalist 513850
GBIF 7306544
Freebase /m/05b4b0b
EPPO SALCD
EOL 6341823
Elurikkus 661886
Wikipedia Salvia_candidissima

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
Chemometric Analysis Evidencing the Variability in the Composition of Essential Oils in 10 Salvia Species from Different Taxonomic Sections or Phylogenetic Clades Tomou EM, Fraskou P, Dimakopoulou K, Dariotis E, Krigas N, Skaltsa H Molecules 29-Mar-2024
PMCID:PMC11013157
doi:10.3390/molecules29071547
PMID:38611827
Screening of 20 species from Lamiaceae family based on phytochemical analysis, antioxidant activity and HPLC profiling Moshari-Nasirkandi A, Alirezalu A, Alipour H, Amato J Sci Rep 09-Oct-2023
PMCID:PMC10562417
doi:10.1038/s41598-023-44337-7
PMID:37813985
Diterpenoids from Roots of Salvia lachnocalyx; In-silico and In-vitro Toxicity against Human Cancer Cell Lines Hadavand Mirzaei H, Firuzi O, Jassbi AR Iran J Pharm Res 01-Sep-2020
PMCID:PMC8019878
doi:10.22037/ijpr.2019.15429.13095
PMID:33841524
Potential anti-influenza effective plants used in Turkish folk medicine: A review Sargin SA J Ethnopharmacol 31-Aug-2020
PMCID:PMC7458060
doi:10.1016/j.jep.2020.113319
PMID:32882361
A New Ferula (Apiaceae) Species from Southwest Anatolia: Ferula pisidica Akalın & Miski Akalın E, Tuncay HO, Olcay B, Miski M Plants (Basel) 12-Jun-2020
PMCID:PMC7355485
doi:10.3390/plants9060740
PMID:32545501
Effect-Directed Analysis for the Antioxidant Compound in Salvia verticillata Nickavar B, Rezaee J, Nickavar A Iran J Pharm Res 01-Jan-2016
PMCID:PMC4986120
PMID:27610164
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227
Terpenoids and flavonoids from the aerial parts of Salvia candidissima G. Topcu, N. Tan, A. Ulubelen, D. Sun, W.H. Watson Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00245-3
Terpenoids from Salvia candidissima subsp. candidissima Ayhan Ulubelen, Nur Tan, Gülaçti Topcu Elsevier BV 25-Mar-2003
doi:10.1016/S0031-9422(97)00146-5
Diterpenoids from Salvia candidissima Ayhan Ulubelen, Gülaçti Topcu, Nur Tan Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)60883-3
Composition of essential oils from turkish Salvia species Ali Bayrak, Attila Akgül Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84802-5
Rearranged abietane diterpenes from Salvia candidissima A. Ulubelen, G. Topcu, N. Tan Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83745-K

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2,4-Dimethoxybenzoic acid 7052 Click to see COC1=CC(=C(C=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1016/0031-9422(95)00245-3
> Benzenoids / Naphthalenes
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione 10495322 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(1S)-1-hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one 163016674 Click to see CC1=C2CCCC(=C)CC3(C2=C(C=C1)C=C(C3=O)C(C)C)O 296.40 unknown https://doi.org/10.1016/S0040-4039(00)60883-3
1-Hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one 102011357 Click to see 296.40 unknown https://doi.org/10.1016/S0040-4039(00)60883-3
https://doi.org/10.1016/S0031-9422(97)00146-5
Microstegiol 403772 Click to see 298.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
https://doi.org/10.1016/S0031-9422(97)00146-5
> Benzenoids / Naphthalenes / Naphthoquinones
1-Ketoaethiopinone 11983338 Click to see 310.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
4-Hydroxy-7-methyl-8-(4-methyl-3-oxopent-4-enyl)-3-propan-2-ylnaphthalene-1,2-dione 101931842 Click to see 326.40 unknown https://doi.org/10.1016/0031-9422(95)00245-3
Aethiopinone 157301 Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C 296.40 unknown https://doi.org/10.1016/S0040-4039(00)60883-3
Salvipisone 821448 Click to see 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/0031-9422(92)83745-K
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,10aS)-10a-hydroxy-1,4a-dimethyl-4-oxo-7-propan-2-yl-2,3,9,10-tetrahydrophenanthrene-1-carboxylic acid 101712284 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(1R,8R,10R)-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol 138113902 Click to see 316.40 unknown https://doi.org/10.1016/S0040-4039(00)60883-3
(4aR,10aR)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162993082 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC 330.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(4aR)-5,6,8-trihydroxy-4a-(methoxymethyl)-1,1-dimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 101712283 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(4aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 162958596 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol 101219048 Click to see 316.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 15241261 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
10a-Hydroxy-1,4a-dimethyl-4-oxo-7-propan-2-yl-2,3,9,10-tetrahydrophenanthrene-1-carboxylic acid 163009620 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
11-Hydroxy-12-Methoxyabietatriene 14827262 Click to see 316.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/0031-9422(92)83745-K
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-4-ol 14827261 Click to see 316.50 unknown https://doi.org/10.1016/0031-9422(92)83745-K
https://doi.org/10.1016/S0031-9422(97)00146-5
4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 73189945 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C 300.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 162958595 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 5316143 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC 330.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 10935937 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5,6,8-trihydroxy-4a-(methoxymethyl)-1,1-dimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 162878892 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
7-Acetylhorminone 2751796 Click to see 374.50 unknown https://doi.org/10.1016/0031-9422(92)83745-K
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
cis-Ferruginol 91747538 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Cryptanol 184179 Click to see 316.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
Cryptojaponol 11724205 Click to see 330.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/0031-9422(92)83745-K
Horminone 2751795 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
Manool 3034394 Click to see 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Salvinolone 11723174 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1016/0031-9422(92)83745-K
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84802-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
beta-Spathulenol 522266 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(95)00245-3
Spathulenol 92231 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(95)00245-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,4aR,6aS,10aS,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-1-ol 101931843 Click to see 306.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/0031-9422(95)00245-3
(3S,4aS,6aS,10aS,10bR)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene 98133973 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(95)00245-3
[(3R,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] hexadecanoate 101712285 Click to see 665.10 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
[17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1-oxo-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] hexadecanoate 85741702 Click to see 665.10 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-1-ol 162987617 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(95)00245-3
https://doi.org/10.1016/S0031-9422(97)00146-5
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene 518574 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(95)00245-3
https://doi.org/10.1016/S0031-9422(97)00146-5
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/S0040-4039(00)60883-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(3R)-3-[(1R,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-4-en-1-ol 163006519 Click to see CC1(CCCC2(C1CCC(=C)C2C(C)(CCO)C=C)C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
3-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-4-en-1-ol 163006518 Click to see 290.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,2R,4aS,8aS)-1-[(3R)-5-hydroxy-3-methylpent-1-en-3-yl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 162935254 Click to see 308.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
1-(5-hydroxy-3-methylpent-1-en-3-yl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 162935253 Click to see 308.50 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1Z,5S,12Z)-5-hydroxy-12-methyl-7-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-1(14),2,9(15),12-tetraen-4-one 162871303 Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(CC1)CC(=C)C3)O)C(C)C 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
(5S)-5-hydroxy-6,6,11-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-1(13),2,9(14),11-tetraen-4-one 163093447 Click to see 298.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5-Hydroxy-12-methyl-7-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-1(14),2,9(15),12-tetraen-4-one 162871302 Click to see 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
5-Hydroxy-6,6,11-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-1(13),2,9(14),11-tetraen-4-one 163093446 Click to see CC1=CC=C2C=C(C(=O)C3(C2=C(C1)CCC3(C)C)O)C(C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Eicosyl p-coumarate 15139446 Click to see 444.70 unknown https://doi.org/10.1016/0031-9422(95)00245-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Mikanin 15560536 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1016/0031-9422(95)00245-3
> 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/10.1016/0031-9422(95)00245-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin 161271 Click to see 328.30 unknown https://doi.org/10.1016/S0031-9422(97)00146-5
https://doi.org/10.1016/0031-9422(95)00245-3

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.