Details Top

Internal ID UUID643fded333970970330195
Scientific name Lathyrus tingitanus
Authority L.
First published in Sp. Pl.: 732 (1753)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Ornamental cut flower and garden plant: Lathyrus tingitanus is listed in horticultural databases (e.g., Royal Horticultural Society Plant Finder) as an annual climber grown for its bright pink to magenta flowers. It is used in floral arrangements, as a bedding plant, and for container displays and trellis plantings in temperate gardens.
- Forage legume for livestock: The species is cultivated as a forage legume, providing a protein‑rich feed for grazing animals. It appears in forage legume profiles (e.g., FAO Grassland Species Profiles) and is valued for its high biomass production in Mediterranean climates.

Properties relevant to use:
- Nitrogen fixation: As a legume, L. tingitanus forms symbiotic nodules with rhizobia, fixing atmospheric nitrogen and contributing to soil fertility when used as a cover crop or in rotations.
- Growth habit and agronomic traits: The plant is an annual herb reaching 30–80 cm, with rapid vegetative growth that enables quick ground cover and weed suppression. Its self‑pollinating nature simplifies seed production.
- Feed quality: When harvested as forage, it yields substantial dry matter; feed composition tables report relatively high crude protein levels, supporting its use in mixed pastures.
- Ornamental value: The species produces showy, colorful flowers attractive to pollinators and is cultivated primarily for visual appeal rather than for industrial extractives.
- Research applications: L. tingitanus is employed as a model legume in studies of symbiotic nitrogen fixation, nodulation physiology, and genetic diversity; published work documents nodule formation and molecular marker analysis of natural populations.

Sustainability and sourcing:
- Native to the western Mediterranean (Spain, Morocco, Tunisia), L. tingitanus is adapted to low‑input, dryland conditions and can be cultivated with minimal irrigation and fertilizer inputs.
- Its role as a nitrogen‑fixing cover crop reduces the need for synthetic nitrogen fertilizers, supporting sustainable cropping systems.
- Seed is produced locally in Mediterranean nurseries and is commercially available through ornamental and forage seed suppliers, allowing diversified sourcing and on‑farm seed saving.
- The plant’s annual lifecycle and self‑pollinating habit facilitate integration into crop rotations and intercropping systems, contributing to soil health and biodiversity.

Synonyms Top

Scientific name Authority First published in
Lathyrus mexicanus Wender. Index Seminum (MB, Marburgensis)1837: [4] (1837)
Lathyrus coruscans Emb. & Maire M.L.Emberger, Pl. Marocc. Nov.2: 4 (1929)
Lathyrus aegyptiacus Hasselq. Iter Palaest.: 482 (1757)
Navidura tingitana Alef. Bonplandia (Hannover)9: 147 (1861)
Clymenum tingitanum (L.) Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 358 (1787)
Lathyrus tingitanus f. granatensis Lacaita Cavanillesia1: 10 (1928)
Lathyrus tingitanus var. coruscans (Emb. & Maire) Maire É.Jahandiez & al., Cat. Pl. Maroc2: 436 (1932)
Lathyrus napoleonis Voss Vilm. Blumengärtn., ed. 3. 1: 212 (1894)
Lathyrus pulcher Salisb. Prodr. Stirp. Chap. Allerton : 338 (1796)

Common names Top

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Language Common/alternative name
English tangier pea
Arabic جلبان طنجي
Czech hrachor tangerský
German tanger-platterbse
Latvian spānijas dedestiņa
Swedish spanskvial
Chinese 地中海香豌豆

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
plant in deep pot

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Middle Europe
      • Czechoslovakia
    • Southwestern Europe
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Southwest
    • Northwestern U.S.A.
      • Idaho
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212708
USDA Plants LATI
Tropicos 13021749
INPN 105271
Flora of Italy 2495
KEW urn:lsid:ipni.org:names:502046-1
The Plant List ild-7781
Open Tree Of Life 510040
Observations.org 147878
NCBI Taxonomy 3862
NBN Atlas NBNSYS0200003879
Nature Serve 2.153456
IUCN Red List 176447
IPNI 502046-1
iNaturalist 61821
GBIF 5356578
Freebase /m/047mlcd
EPPO LTHTI
EOL 703187
Calflora (Californian flora) 4624
USDA GRIN 21620
Wikipedia Lathyrus_tingitanus
CMAUP NPO14947

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
Impact of Heat and Drought Stress on Grasspea and Its Wild Relatives Aloui K, Choukri H, El Haddad N, Gupta P, El Bouhmadi K, Emmrich PM, Singh A, Edwards A, Maalouf F, Bouhlal O, Staples J, Kumar S Plants (Basel) 08-Oct-2023
PMCID:PMC10574926
doi:10.3390/plants12193501
PMID:37836241
Characterization of the complete chloroplast genome of Canavalia gladiata Zhao J Mitochondrial DNA B Resour 27-Jan-2021
PMCID:PMC7850338
doi:10.1080/23802359.2020.1861566
PMID:33553637
Initial Characterization of the Chloroplast Genome of Vicia sepium, an Important Wild Resource Plant, and Related Inferences About Its Evolution Li C, Zhao Y, Xu Z, Yang G, Peng J, Peng X Front Genet 20-Feb-2020
PMCID:PMC7044246
doi:10.3389/fgene.2020.00073
PMID:32153639
Overview of the Structure–Function Relationships of Mannose-Specific Lectins from Plants, Algae and Fungi Barre A, Bourne Y, Van Damme EJ, Rougé P Int J Mol Sci 10-Jan-2019
PMCID:PMC6359319
doi:10.3390/ijms20020254
PMID:30634645
Global analysis of an exponential model of cell proliferation for estimation of cell cycle duration in the root apical meristem of angiosperms Zhukovskaya NV, Bystrova EI, Dubrovsky JG, Ivanov VB Ann Bot 07-Feb-2018
PMCID:PMC6215031
doi:10.1093/aob/mcx216
PMID:29425277
Complete plastid genome of Astragalus membranaceus (Fisch.) Bunge var. membranaceus Wang B, Chen H, Ma H, Zhang H, Lei W, Wu W, Shao J, Jiang M, Zhang H, Jia Z, Liu C Mitochondrial DNA B Resour 23-Jul-2016
PMCID:PMC7800798
doi:10.1080/23802359.2016.1197057
PMID:33473540
Genetic Diversity of Grasspea and Its Relative Species Revealed by SSR Markers Wang F, Yang T, Burlyaeva M, Li L, Jiang J, Fang L, Redden R, Zong X PLoS One 20-Mar-2015
PMCID:PMC4368647
doi:10.1371/journal.pone.0118542
PMID:25793712
Large-scale microsatellite development in grasspea (Lathyrus sativus L.), an orphan legume of the arid areas Yang T, Jiang J, Burlyaeva M, Hu J, Coyne CJ, Kumar S, Redden R, Sun X, Wang F, Chang J, Hao X, Guan J, Zong X BMC Plant Biol 17-Mar-2014
PMCID:PMC4003855
doi:10.1186/1471-2229-14-65
PMID:24635905
Systematics, biogeography, and character evolution of the legume tribe Fabeae with special focus on the middle-Atlantic island lineages Schaefer H, Hechenleitner P, Santos-Guerra A, de Sequeira MM, Pennington RT, Kenicer G, Carine MA BMC Evol Biol 25-Dec-2012
PMCID:PMC3547781
doi:10.1186/1471-2148-12-250
PMID:23267563
A Strong Nucleotypic Effect on the Cell Cycle Regardless of Ploidy Level Francis D, Davies MS, Barlow PW Ann Bot 13-Mar-2008
PMCID:PMC2710215
doi:10.1093/aob/mcn038
PMID:18339642
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457
Lathyrine biosynthesis and the origin of the precursor 2-amino-4-carboxypyrimidine in Lathyrus tingitanus Eric G. Brown, Yusuf Turan Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00436-0
2-Amino-4-carboxypyrimidine in seeds of Lathyrus tingitanus Eric G. Brown Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00987-6
Biosynthesis of lathyrine in lathyrus tingitanus R.C. Hider, D.I. John Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84632-4
Erythro-γ-hydroxyhomo-?-arginine: An amino acid from seed of Lonchocarpus costaricensis, and its preferential interaction with borate S Evans Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81117-6

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine 485077 Click to see 349.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
Methyl 9H-pyrido(3,4-b)indole-1-carboxylate 597266 Click to see 226.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl Syringate 70164 Click to see 212.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
3,4,5-Trimethoxybenzyl alcohol 77449 Click to see 198.22 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Coniferaldehyde 5280536 Click to see 178.18 unknown via CMAUP database
Feruloyltyramine 5280537 Click to see 313.30 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin 179651 Click to see 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
CID 9848259 9848259 Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C 486.50 unknown via CMAUP database
Evodol 185481 Click to see 484.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
2-[2-(4-Amino-5-oxooxolan-2-yl)ethyl]guanidine 536750 Click to see C1C(OC(=O)C1N)CCN=C(N)N 186.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1202897/
2-[2-[(2S,4R)-4-amino-5-oxooxolan-2-yl]ethyl]guanidine 163020400 Click to see 186.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1202897/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-6-guanidino-4-hydroxyhexanoic acid 4479244 Click to see C(CN=C(N)N)C(CC(C(=O)O)N)O 204.23 unknown https://doi.org/10.1016/S0031-9422(00)84632-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R,4S)-2-amino-6-(diaminomethylideneamino)-4-hydroxyhexanoic acid 134687319 Click to see 204.23 unknown https://doi.org/10.1016/S0031-9422(00)84632-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Homoarginine 9085 Click to see 188.23 unknown https://doi.org/10.1016/S0031-9422(00)81117-6
Lathyrine 166766 Click to see 182.18 unknown https://doi.org/10.1016/S0031-9422(96)00436-0
https://doi.org/10.1016/0031-9422(90)80168-G
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-O-Caffeoylquinic acid methyl ester 6476139 Click to see 368.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2S)-2-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one 12181418 Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O 196.20 unknown via CMAUP database
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidinecarboxylic acids and derivatives / Pyrimidinecarboxylic acids
2-Aminopyrimidine-4-carboxylic acid 247194 Click to see 139.11 unknown https://doi.org/10.1016/0031-9422(95)00987-6
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Hortiacine 378227 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC=CC=C5C4=O 317.30 unknown via CMAUP database
Rutaecarpine 65752 Click to see 287.30 unknown via CMAUP database
Strychnocarpine 162871 Click to see 200.24 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine 179640 Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O 319.30 unknown via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
Oxychelerythrine 147279 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC 363.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine 164950 Click to see 215.20 unknown via CMAUP database
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
Paprazine 5372945 Click to see 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Evofolin C 44445795 Click to see 218.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fraxin 5273568 Click to see 370.31 unknown via CMAUP database
Isofraxoside 11508953 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 370.31 unknown via CMAUP database
Skimmin 99693 Click to see 324.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Sophoraflavone B 5491513 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone 11625890 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown via CMAUP database
Kaempferol 3-O-beta-D-xyloside 21310440 Click to see 418.30 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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