Details Top

Internal ID UUID643fdef7785ee370343904
Scientific name Calicotome villosa
Authority (Poir.) Link
First published in Neues J. Bot.2(2): 51 (1808)

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.

Candlestick broom is a sun-loving, spiny Mediterranean shrub with bright yellow flowers. In traditional practice, infusions and decoctions of its flowering tops and tender shoots have been used as mild febrifuges and sedatives, and as digestive tonics in North Africa, while in southern Spain an infusion of the flowering tops has been taken as a diuretic and to settle the stomach. In Malta, a traditional remedy from the same plant parts has been used for colds and sore throats; in Algeria a gentle infusion is valued for calming children and as a low‑dose antispasmodic. Alongside drinks, poultices of fresh young stems or leaf extracts have been applied to swellings and rheumatic pains; in Morocco such preparations are reported for headache and bruises as well as burns.

Among the Maltese, the Sicilian–Maltese herbal tradition notes a simple infusion: steep 5–10 g of fresh flowering tops in 250 ml of near‑boiling water for 10 minutes, strain, and drink a small cup 1–2 times daily as needed. In North Africa, herbalists prepare a decoction for fevers by simmering 20 g of flowering tops in 1 L of water for 15 minutes, cooling, and taking 50–100 ml up to three times daily. A maceration for topical use is made by crushing fresh tender shoots with a little water to a pulp and applying the poultice to the affected area for 20–30 minutes, once or twice daily. Known constituents include flavonoids such as quercetin and kaempferol glycosides, phenolic acids including chlorogenic acid, and low levels of quinolizidine alkaloids like cytisine that have mild stimulant activity; the alkaloids help explain traditional sedo‑relaxant reports while the flavonoids support the mild diuretic and febrifuge roles.

As a Mediterranean wild shrub, C. villosa remains locally harvested and occasionally appears in small‑batch herbal blends, though it is not a mainstream commercial item. Contemporary pharmacology in Europe and North Africa is focused on profiling its flavonoids and quinolizidine alkaloids, and on validating traditional diuretic and anti‑inflammatory claims in vitro and in small clinical trials in Tunisia and Spain.

General Uses Top

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Common products:
- Wood for small tools and handles (heartwood/sapwood)
- Fiber products (bast fiber cordage/rope)
- Animal fodder (cut forage)
- Honey feedstock (floral nectar)

Industrial and craft applications:
- Tannin extracts for leather tanning (bark tannins)
- Natural dye production (yellow pigments from flowers)
- Small woodcraft items (tool handles, walking sticks)

Food and beverages (non-medicinal):
- Honey production (monofloral honey from flower nectar)

Colorants and tanning:
- Natural yellow dye (floral pigments)
- Vegetable tanning agent (bark, classified as hydrolyzable tannins)

Wood and fiber:
- Durable small timber objects (dense hardwood)
- Coarse fiber cordage (bast fiber from stems)

Properties relevant to use:
- Tannins concentrated in bark (high hydrolyzable tannin content facilitating leather processing)
- Fiber strength suitable for rope-making (lignocellulosic bast fiber composition)
- Dense, durable heartwood (high lignin content in mature wood)

Sustainability and sourcing:
- Harvested from wild populations in Mediterranean sclerophyllous habitats
- Potential overharvesting risk in some regions due to fodder demand
- Propagation possible through seed collection and nursery production

Synonyms Top

Scientific name Authority First published in
Lygoplis villosum (Poir.) Raf. Sylva Tellur.: 23 (1838)
Laburnum lanigerum J.Presl F.Berchtold & J.S.Presl, Prir. Rostlin Aneb. Rostl.3: 100 (1830)
Cytisus preslii Nyman Syll. Fl. Eur.: 283 (1855)
Cytisus lanigerus DC. Prodr.2: 154 (1825)
Spartium villosum Poir. Voy. Barbarie2: 207 (1789)
Calicotome spinosa subsp. villosa (Poir.) Rouy G.Rouy & J.Foucaud, Fl. France4: 249 (1897)
Calicotome spinosa var. villosa (Poir.) Fiori & Paoletti A.Fiori & al., Fl. Anal. Italia2: 23 (1900)
Calicotome villosa var. cretica Rothm. Bot. Jahrb. Syst.72: 186 (1949)
Calicotome spinosa var. macrantha Rouy G.Rouy & J.Foucaud, Fl. France4: 249 (1897)
Calicotome cretica C.Presl Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 481 (1845)
Genista lanigera (DC.) Scheele Flora26: 438 (1843)
Genista villosa (Poir.) Spach Ann. Sci. Nat., Bot. , sér. 3, 3: 156 (1845)
Spartium lanigerum Desf. Fl. Atlant. 2: 135 (1798)
Calicotome villosa var. genuina Rothm. Bot. Jahrb. Syst. 72: 284 (1949)
Calicotome spinosa var. genuina Rouy Fl. France 4: 249 (1897)
Spartium spinosum Brot. Fl. Lusit. 2: 85 (1804)

Common names Top

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Language Common/alternative name
Spanish herguen
Spanish spartium villosum
Spanish spartium lanigerum
Spanish laburnum lanigerum
Spanish calicotome spinosa var. genuina
Spanish calicotome spinosa subsp. villosa
Spanish jérguenes
Spanish jerguenes
Spanish jerguén
Spanish jerguen
Spanish hérguenes
Spanish herguenes
Spanish erguene
Arabic قندول شعري
Greek Σπαλαθκιά
Greek Ασπάλαθος
Hebrew קדה שעירה
Hebrew קידה שעירה
Dutch aspalathos

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
  • Asia-temperate
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
    • Southwestern Europe
      • Corse
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000213265
Tropicos 13072301
INPN 792094
KEW urn:lsid:ipni.org:names:77106062-1
The Plant List ild-8336
PFAF Calicotome villosa
PaleoBotany 64334
Open Tree Of Life 259877
Observations.org 149860
NCBI Taxonomy 49799
IPNI 77106062-1
iNaturalist 340941
GBIF 2956364
EPPO CCOVI
EOL 703764
USDA GRIN 8671
Wikipedia Calicotome_villosa
CMAUP NPO22983

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
Prevalence of nonalcoholic fatty liver disease and liver cirrhosis in Chinese adults with type 2 diabetes mellitus Han X, Zhang X, Liu Z, Fan H, Guo C, Wang H, Gu Y, Zhang T J Diabetes 25-Apr-2024
PMCID:PMC11045916
doi:10.1111/1753-0407.13564
PMID:38664879
Enhancing Pisum sativum growth and symbiosis under heat stress: the synergistic impact of co-inoculated bacterial consortia and ACC deaminase-lacking Rhizobium Ben Gaied R, Sbissi I, Tarhouni M, Brígido C Arch Microbiol 04-Apr-2024
PMCID:PMC10995081
doi:10.1007/s00203-024-03943-3
PMID:38573536
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
Ecological and Syntaxonomic Analysis of the Communities of Glebionis coronaria and G. discolor (Malvion neglectae) in the European Mediterranean Area Cano E, Cano-Ortiz A, Quinto Canas R, Piñar Fuentes JC, Rodrigues Meireles C, Raposo M, Pinto Gomes C, Laface VL, Spampinato G, Musarella CM Plants (Basel) 20-Feb-2024
PMCID:PMC10934477
doi:10.3390/plants13050568
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Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Bacterial Endophytes from Legumes Native to Arid Environments Are Promising Tools to Improve Mesorhizobium–Chickpea Symbiosis under Salinity Ben Gaied R, Sbissi I, Tarhouni M, Brígido C Biology (Basel) 03-Feb-2024
PMCID:PMC10886315
doi:10.3390/biology13020096
PMID:38392314
Variovorax sp. strain P1R9 applied individually or as part of bacterial consortia enhances wheat germination under salt stress conditions Acuña JJ, Rilling JI, Inostroza NG, Zhang Q, Wick LY, Sessitsch A, Jorquera MA Sci Rep 24-Jan-2024
PMCID:PMC10808091
doi:10.1038/s41598-024-52535-0
PMID:38267517
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
Environmental DNA: The First Snapshot of the Vertebrate Biodiversity in Three Sicilian Lakes Mauro M, Lo Valvo M, Vazzana M, Radovic S, Vizzini A, Badalamenti R, Hornsby LB, Arizza V Animals (Basel) 28-Nov-2023
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Mechanistic insights into nitrogen-induced changes in pasting characteristics of rice during storage based on proteomics analysis Liang H, Gu B, Sun W, Li B, Qu H, Tao D, Zhang Q, Wang T, Ma Y, Wang Y, Wu Z, Zhang Q Food Chem X 20-Nov-2023
PMCID:PMC10740089
doi:10.1016/j.fochx.2023.101018
PMID:38144749
Natural Antimicrobials: A Reservoir to Contrast Listeria monocytogenes Ricci A, Lazzi C, Bernini V Microorganisms 15-Oct-2023
PMCID:PMC10609241
doi:10.3390/microorganisms11102568
PMID:37894226
A single-point modeling approach for the intercomparison and evaluation of ozone dry deposition across chemical transport models (Activity 2 of AQMEII4) Clifton OE, Schwede D, Hogrefe C, Bash JO, Bland S, Cheung P, Coyle M, Emberson L, Flemming J, Fredj E, Galmarini S, Ganzeveld L, Gazetas O, Goded I, Holmes CD, Horváth L, Huijnen V, Li Q, Makar PA, Mammarella I, Manca G, Munger JW, Pérez-Camanyo JL, Pleim J, Ran L, Jose RS, Silva SJ, Staebler R, Sun S, Tai AP, Tas E, Vesala T, Weidinger T, Wu Z, Zhang L Atmos Chem Phys 06-Sep-2023
PMCID:PMC10659075
doi:10.5194/acp-23-9911-2023
PMID:37990693
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
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PMCID:PMC9920315
doi:10.3390/plants12030655
PMID:36771739
Suspicions of two bridgehead invasions of Xylella fastidiosa subsp. multiplex in France Dupas E, Durand K, Rieux A, Briand M, Pruvost O, Cunty A, Denancé N, Donnadieu C, Legendre B, Lopez-Roques C, Cesbron S, Ravigné V, Jacques MA Commun Biol 27-Jan-2023
PMCID:PMC9883466
doi:10.1038/s42003-023-04499-6
PMID:36707697

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1016/S0367-326X(03)00061-3
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/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl p-coumarate 92203 Click to see 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol 11095 Click to see 288.25 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
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/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Isorhamnetin 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside 5487249 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown via CMAUP database
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyoxan-2-yl]methyl acetate 21580050 Click to see 458.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
[(2S,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyoxan-3-yl] acetate 163103889 Click to see 458.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
[3,4,5-Trihydroxy-6-(5-hydroxy-4-oxo-2-phenylchromen-7-yl)oxyoxan-2-yl]methyl acetate 73804357 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=CC=C4)O)O)O)O 458.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
[6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 13845966 Click to see 490.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
5-Hydroxy-2-phenyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 15558424 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Chrysin-7 beta-monoglucoside 5490092 Click to see 416.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Hesperetin-7-Rutinoside 3594 Click to see 610.60 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Hesperidin 10621 Click to see 610.60 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
luteolin 7-O-6''-acetylglucoside 21721976 Click to see 490.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Sinensin 10456395 Click to see 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 21676216 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O)O 448.40 unknown via CMAUP database
5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 20831111 Click to see 462.40 unknown via CMAUP database
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Genistein 7,4'-di-O-beta-D-glucopyranoside 91431845 Click to see 594.50 unknown via CMAUP database
Genistin 5281377 Click to see 432.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Sissotrin 5280781 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)prop-2-en-1-one 2483 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
3-(3,4-Dihydroxyphenyl)-1-(2-hydroxy-4-methoxyphenyl)prop-2-en-1-one 2535 Click to see 286.28 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Butein 5281222 Click to see 272.25 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
Calythropsin 5353470 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC(=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 25201046 Click to see 270.28 unknown https://doi.org/10.1016/S0367-326X(03)00061-3
4,4'-Dihydroxy-2'-methoxychalcone 5319688 Click to see 270.28 unknown https://doi.org/10.1016/S0367-326X(03)00061-3

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