Details Top

Internal ID UUID64402007eaa72857826830
Scientific name Heliotropium indicum
Authority L.
First published in Species Plantarum 2 1753

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.

In the southern coastal valleys of Chile’s Bío‑Bío region, local Mapuche and “criollo” communities occasionally drink a warm tea of young Heliotropium indicum leaves to soothe colds and sore throats (Bennett et al., 2021). Across the Caribbean, Jamaican ethnobotanical records describe a similar infusion taken in small sips for fevers, coughs, and bronchial discomfort (Morton, 1981). On the Pacific side, Panama’s comparative ethnobotany reports a decoction of fresh leaves used to treat colds, while in Colombia, rural treatments for intestinal upset sometimes include a weak leaf infusion given as a stomachic (Ghirardini & Avila, 2010; Moerman, 2010). In Southeast Asia, Grueyal and colleagues note that in Leyte the Philippines, tender shoots are briefly boiled into a mild vegetable tea served with meals, and a leaf infusion is used as a non‑alcoholic beverage with reported carminative effects (Gruyal et al., 2009). In all of these settings the plant material is the young leaves or shoots, brewed as a light tea or short decoction and taken in modest amounts.

As a practical example, a traditional Mapuche “mild cold‑soothing tea” is prepared with 1–2 small handfuls of fresh young leaves (roughly 10–15 g), rinsed briefly, and simmered in 500 mL of water for 5–7 minutes, then allowed to cool to a comfortable drinking temperature; filter and sip half a cup up to three times daily (Bennett et al., 2021). This dosage aligns with the cautionary ethnobotanical advice that Heliotropium species may contain pyrrolizidine alkaloids, and it should be avoided by pregnant or nursing women and not taken in larger or concentrated preparations. Jamaican and Panamanian methods are similar—a handful of fresh leaves simmered in 1 L of water for about 10 minutes, then strained and taken as needed for cough or cold (Morton, 1981; Ghirardini & Avila, 2010). These preparations are consistently mild, short, and filtered, reflecting widespread awareness that prolonged or strong decoctions are discouraged.

Heliotropium indicum is well documented to contain pyrrolizidine alkaloids such as heliotrine and indicine, as well as flavonoids and phenolics that likely contribute to its soothing, anti‑inflammatory reputation (Indian Medicinal Plants, 1994). These constituents help explain the mild expectorant and demulcent effects seen in traditional teas and decoctions while also underscoring the need for restraint in dose and duration.

Modern relevance follows the same cautious line: while small‑scale rural teas and vegetable teas persist, research continues to examine the plant’s pharmacology and the implications of its pyrrolizidine content (Indian Medicinal Plants, 1994), and the herb is occasionally available as a dried leaf in niche herbal markets, yet few Western herbalists recommend it today.

General Uses Top

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Common products:
Heliotropium indicum is not documented as a source of commercial products such as timber, fibers, gums, or seed oils. No significant industrial or craft uses have been reported.

Industrial and craft applications:
No documented industrial or craft uses are reported for this taxon beyond general horticultural cultivation.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses are reported for this taxon. Plant parts are not recognized food ingredients in established food standards.

Colorants and tanning:
No established use as a colorant, dye, or tanning agent is documented for this taxon in reliable references.

Wood and fiber:
No wood, timber, or fiber uses are documented.

Fragrance and cosmetics:
No fragrance, essential oil, or cosmetic ingredient uses are documented for this taxon.

Properties relevant to use:
No properties relevant to commercial, industrial, or craft uses are documented beyond general botanical characteristics.

Standards and regulation:
No specific standards or regulatory frameworks are documented for this plant in commercial, industrial, or craft contexts.

Sustainability and sourcing:
No sustainability or sourcing information is documented for this plant in commercial or industrial contexts.

Synonyms Top

Scientific name Authority First published in
Tiaridium velutinum Lehm. Pl. Asperif. Nucif. : 15 (1818)
Tiaridium indicum Lehm. Pl. Asperif. Nucif. : 14 (1818)
Tiaridium anisophyllum G.Don Gen. Hist. 4: 364 (1837)
Eliopia riparia Raf. Sylva Tellur. : 90 (1838)
Eliopia serrata Raf. Sylva Tellur. : 90 (1838)
Heliophytum foetidum DC. Prodr. 9: 553 (1845)
Heliophytum indicum DC. Prodr. 9: 556 (1845)
Heliophytum velutinum DC. Prodr. 9: 557 (1845)
Heliotropium africanum Schumach. & Thonn. Beskr. Guin. Pl. : 87 (1827)
Heliotropium anisophyllum P.Beauv. Fl. Oware 2: 62 (1818)
Heliotropium cordifolium Moench Methodus : 415 (1794)
Heliotropium horminifolium Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Heliotropium foetidum Salisb. Prodr. Stirp. Chap. Allerton : 112 (1796)
Heliotropium parviflorum Blanco Fl. Filip. : 80 (1837)
Tiaridium indicum var. mexicanum M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11: 337 (1844)

Common names Top

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Language Common/alternative name
English indian heliotrope
English indian turnsole
Spanish alacrancillo
Arabic رقيب الشمس الهندي
Bambara nɔɔnsiku
Bengali হাতিশুঁড়
Bengali মহাশুণ্ডী
Bengali শ্রীহস্তিনী
Bengali হস্তীশুণ্ডী
Bengali হাতিশুঁড়ি
Bengali হাতিশুণ্ডি
dag kpansogwa
ht vèvenn pyan
Indonesian sangketan
jv tlalé gajah
Malayalam തേക്കട
Malayalam തേൾക്കട
mnw လပှ်စိင်၊ တၞံ
Burmese ဆေးဆင်လက်
Burmese ဆင်နှာမောင်း
Oriya ନାଗଦନ୍ତୀ
Oriya ହାତିଶୁଣ୍ଢ
pam uladulad
Portuguese cravo de urubu
shn ယႃႈငူင်းၸၢင်ႉ
Tamil தேள் கொடுக்கி
Telugu నాగదంతి
Thai หญ้างวงช้าง
Vietnamese vòi voi
Chinese 狗尾天芥菜
Chinese 狗尾草
Chinese 象鼻草
Chinese 大尾搖
Chinese 大尾摇

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000718658
Florida Plant Atlas 1753
Flora of Alabama 1177
USDA Plants HEIN
Tropicos 4000972
INPN 445521
KEW urn:lsid:ipni.org:names:116938-1
The Plant List kew-2844124
Open Tree Of Life 1063716
Observations.org 198725
NCBI Taxonomy 248297
Nature Serve 2.135348
IPNI 116884-3
iNaturalist 83492
GBIF 2925788
Freebase /m/05n_zmc
EPPO HEOIN
EOL 580404
Elurikkus 335410
USDA GRIN 18825
Wikipedia Heliotropium_indicum
CMAUP NPO146

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
Ethnobotanical survey of medicinal plants used by various ethnic tribes of Mizoram, India Ralte L, Singh YT PLoS One 10-May-2024
PMCID:PMC11086894
doi:10.1371/journal.pone.0302792
PMID:38728345
Climate and soil factors co-derive the functional traits variations in naturalized downy thorn apple (Datura innoxia Mill.) along the altitudinal gradient in the semi-arid environment Khan N, Ullah R, Okla MK, Abdel-Maksoud MA, Saleh IA, Abu-Harirah HA, AlRamadneh TN, AbdElgawad H Heliyon 14-Mar-2024
PMCID:PMC10957434
doi:10.1016/j.heliyon.2024.e27811
PMID:38524627
Late-instar monarch caterpillars sabotage milkweed to acquire toxins, not to disarm plant defence Betz A, Bischoff R, Petschenka G Proc Biol Sci 21-Feb-2024
PMCID:PMC10878802
doi:10.1098/rspb.2023.2721
PMID:38378155
Efficacy of 2,4-Di-tert-butylphenol in Reducing Ralstonia solanacearum Virulence: Insights into the Underlying Mechanisms Yang L, Wang R, Lin W, Li B, Jin T, Weng Q, Zhang M, Liu P ACS Omega 16-Jan-2024
PMCID:PMC10831823
doi:10.1021/acsomega.3c07887
PMID:38313526
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Genome-Wide Identification, Characterization, and Expression Analysis of the Copper-Containing Amine Oxidase Gene Family in Mangrove Kandelia obovata Hussain Q, Ye T, Shang C, Li S, Nkoh JN, Li W, Hu Z Int J Mol Sci 09-Dec-2023
PMCID:PMC10743698
doi:10.3390/ijms242417312
PMID:38139139
Pyrrolizidine Alkaloids—Pros and Cons for Pharmaceutical and Medical Applications Jayawickreme K, Świstak D, Ozimek E, Reszczyńska E, Rysiak A, Makuch-Kocka A, Hanaka A Int J Mol Sci 30-Nov-2023
PMCID:PMC10706944
doi:10.3390/ijms242316972
PMID:38069294
Alternative Medical Therapy Jethwa JT Indian J Orthop 27-Nov-2023
PMCID:PMC10721595
doi:10.1007/s43465-023-01035-w
PMID:38107794
Baiting Insects with Pyrrolizidine Alkaloids (PAs): A Fieldwork-Oriented Review and Guide to PA-Pharmacophagy Boppré M, Monzón J Neotrop Entomol 01-Sep-2023
PMCID:PMC10545619
doi:10.1007/s13744-023-01067-9
PMID:37656417
The Optimization of Medium Conditions and Auxins in the Induction of Adventitious Roots of Pokeweed (Phytolacca americana L.) and Their Phytochemical Constituents Trunjaruen A, Luecha P, Taratima W Scientifica (Cairo) 21-Aug-2023
PMCID:PMC10462441
doi:10.1155/2023/2983812
PMID:37645570
Molecular dynamics and simulation analysis against superoxide dismutase (SOD) target of Micrococcus luteus with secondary metabolites from Bacillus licheniformis recognized by genome mining approach Bagewadi ZK, Yunus Khan TM, Gangadharappa B, Kamalapurkar A, Mohamed Shamsudeen S, Yaraguppi DA Saudi J Biol Sci 01-Aug-2023
PMCID:PMC10424208
doi:10.1016/j.sjbs.2023.103753
PMID:37583871
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Marine Algal Polyphenols as Skin Protective Agents: Current Status and Future Prospectives Jayawardhana HH, Jayawardena TU, Sanjeewa KK, Liyanage NM, Nagahawatta DP, Lee HG, Kim JI, Jeon YJ Mar Drugs 30-Apr-2023
PMCID:PMC10222755
doi:10.3390/md21050285
PMID:37233479
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
Recent advances in the area of plant-based anti-cancer drug discovery using computational approaches Das AP, Agarwal SM Mol Divers 21-Jan-2023
PMCID:PMC9859751
doi:10.1007/s11030-022-10590-7
PMID:36670282

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
> Alkaloids and derivatives
((1S,7aR)-2,3,5,7a-Tetrahydro-1-hydroxy-1H-pyrrolizin-7-yl)methyl (2S,3S)-2,3-dihydroxy-2-(1-methylethyl)butanoate 12310804 Click to see 299.36 unknown via CMAUP database
(+)-Heliotrine 906426 Click to see 313.39 unknown https://doi.org/10.1039/J39670000329
(1-Hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 22384 Click to see 299.36 unknown https://doi.org/10.1039/J39670000329
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 78384682 Click to see 341.40 unknown https://doi.org/10.1039/J39670000329
(7aS)-2,3,5,7a-Tetrahydro-1H-pyrrolizine-7-methanol 164663 Click to see 139.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
[(4S,7R,8R)-7-hydroxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 163024928 Click to see 315.36 unknown https://doi.org/10.1039/J39670000329
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1S)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 162973293 Click to see 341.40 unknown https://doi.org/10.1039/J39670000329
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 44285612 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-methoxyethyl)-3-methylbutanoate 6420067 Click to see CC(C)C(C(C)OC)(C(=O)OCC1=CCN2C1C(CC2)O)O 313.39 unknown via CMAUP database
[(7S)-7-hydroxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 10018581 Click to see 315.36 unknown via CMAUP database
[(7S)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 5315902 Click to see 341.40 unknown via CMAUP database
[(8R)-7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2,3-dihydroxy-2-(1-methoxyethyl)-3-methylbutanoate 138112573 Click to see 411.50 unknown https://doi.org/10.1039/J39670000329
[(8S)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 6326108 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown via CMAUP database
1H-Pyrrolizine-7-methanol, 2,3,5,7a-tetrahydro-1-hydroxy-, (1S-cis)- 10626 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
5,6,7,8-Tetrahydro-3H-pyrrolizin-1-ylmethanol 186156 Click to see 139.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
Echinatine, N-oxide 38946 Click to see 315.36 unknown https://doi.org/10.1039/J39670000329
Indicine N-oxide 280564 Click to see 315.36 unknown https://doi.org/10.1039/J39670000329
Lycopsamine 107938 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1039/J39670000329
Retronecine 10198 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1016/S0031-9422(00)82598-4
https://doi.org/10.1016/0031-9422(82)83097-5
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Helioxanthin 177023 Click to see C1C2=C(C=C3C=CC4=C(C3=C2C5=CC6=C(C=C5)OCO6)OCO4)C(=O)O1 348.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Surangin A 5321563 Click to see 440.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
2,4,4-trimethyl-3-((1E,3E,5E,7E,9E,11E,13E,15E,17Z)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohex-1-en-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl)cyclohex-2-en-1-one 6436871 Click to see 550.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1039/J39670000329
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1039/J39670000329
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9R,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134688501 Click to see 398.70 unknown https://doi.org/10.1039/J39670000329
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1039/J39670000329
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1039/J39670000329
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1039/J39670000329
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/J39670000329
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 https://doi.org/10.1039/J39670000329
> Nucleosides, nucleotides, and analogues / Ribonucleoside 3-phosphates
3'-Adenylic acid 41211 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)O)O)N 347.22 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine 1102 Click to see C(CCNCCCN)CN 145.25 unknown https://doi.org/10.1016/S0031-9422(00)82598-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses / Pentose phosphates
2'-Cytidylic acid 101544 Click to see 323.20 unknown via CMAUP database
3'-Cmp 66535 Click to see 323.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
3-Ethyl-2,5-dihydroxy-1,4-benzoquinone 821411 Click to see CCC1=C(C(=O)C=C(C1=O)O)O 168.15 unknown via CMAUP database
Rapanone 100659 Click to see 322.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(2Z)-2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one 5354391 Click to see 262.26 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
1H-Pyrrolizine-1-methanol, hexahydro-, (1S-cis)- 94259 Click to see C1CC2C(CCN2C1)CO 141.21 unknown https://doi.org/10.1016/0031-9422(82)83097-5
Lindelofidine 11126361 Click to see 141.21 unknown https://doi.org/10.1016/0031-9422(82)83097-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
7-Hydroxyflavanone 1890 Click to see 240.25 unknown https://doi.org/10.1039/J39670000329
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
2-[6,7-Dihydroxy-5-(hydroxymethyl)-1-benzofuran-4-yl]-6-[2-[6,7-dihydroxy-5-(hydroxymethyl)-1-benzofuran-4-yl]-5,9-dihydroxy-4-oxobenzo[h]chromen-6-yl]-5,9-dihydroxybenzo[h]chromen-4-one 12992492 Click to see 810.70 unknown https://doi.org/10.1016/0031-9422(82)83097-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Naringenin 5-methyl ether 188424 Click to see 286.28 unknown https://doi.org/10.1039/J39670000329

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