Physalis viscosa - Unknown
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Details Top

Internal ID UUID6440416c37f85028998021
Scientific name Physalis viscosa
Authority L.
First published in Sp. Pl. 2: 183. 1753.

Description Top

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Synonyms Top

Scientific name Authority First published in
Cacabus parviflorus Rusby Mem. Torrey Bot. Club 4: 233. 1895
Physalis curassavica L. Sp. Pl. 1: 182. 1753.
Physalis glabriuscula Dunal Prodr. [A. P. de Candolle] 13(1): 436. 1852 [10 May 1852]
Physalis mendocina Phil. Anales Univ. Chile 21: 402. 1862
Physalis pensylvanica L. Sp. Pl., ed. 2. 2: 1670. 1763 [Jul-Aug 1763]

Common names Top

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Language Common/alternative name
English starhair groundcherry
Spanish camambú
gn kamambu
Italian camambù

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Africa
    • Northern Africa
      • Algeria
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Victoria
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile North
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001025039
USDA Plants PHVI17
Tropicos 29601035
INPN 113332
Flora of Italy 8577
KEW urn:lsid:ipni.org:names:817619-1
The Plant List tro-29601035
Open Tree Of Life 264851
Observations.org 150128
NCBI Taxonomy 304129
NBN Atlas NBNSYS0200002872
Nature Serve 2.138665
IPNI 817619-1
iNaturalist 78571
GBIF 5341766
Freebase /m/0b6mvvb
EPPO PHYVI
EOL 581080
Elurikkus 521396
Calflora (Californian flora) 6487
USDA GRIN 102405
Wikipedia Physalis_viscosa

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
Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T Plants (Basel) 18-Mar-2024
PMCID:PMC10975853
doi:10.3390/plants13060872
PMID:38592858
Taxonomic revision of Physalis in Mexico Martínez M, Vargas-Ponce O, Zamora-Tavares P Front Genet 14-Apr-2023
PMCID:PMC10141326
doi:10.3389/fgene.2023.1080176
PMID:37124620
Effect of Rhizome Fragment Length and Burial Depth on the Emergence of a Tropical Invasive Weed Cyperus aromaticus (Navua Sedge) Chadha A, Florentine SK, Dhileepan K, Turville C Plants (Basel) 01-Dec-2022
PMCID:PMC9741406
doi:10.3390/plants11233331
PMID:36501369
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Isolation of Beauveria Strains and Their Potential as Control Agents for Lema bilineata Germar (Coleoptera: Chrysomelidae) Furuie JL, Stuart AK, Voidaleski MF, Zawadneak MA, Pimentel IC Insects 14-Jan-2022
PMCID:PMC8780790
doi:10.3390/insects13010093
PMID:35055935
Changes in antinutrients, phenolics, antioxidant activities and in vitro α-glucosidase inhibitory activity in pumpkin leaves (Cucurbita moschata) during different domestic cooking methods Mashitoa FM, Manhivi V, Slabbert RM, Shai JL, Sivakumar D Food Sci Biotechnol 07-Jun-2021
PMCID:PMC8225750
doi:10.1007/s10068-021-00916-w
PMID:34249384
Optimization of the genotyping‐by‐sequencing SNP calling for diversity analysis in cape gooseberry (Physalis peruviana L.) and related taxa Enciso-Rodríguez FE, Osorio-Guarín JA, Garzón-Martínez GA, Delgadillo-Duran P, Barrero LS PLoS One 26-Aug-2020
PMCID:PMC7449456
doi:10.1371/journal.pone.0238383
PMID:32845934
Effects of Rhizome Length and Planting Depth on the Emergence and Growth of Alepidea amatymbica Eckl. & Zeyh Mangoale RM, Afolayan AJ Plants (Basel) 10-Jun-2020
PMCID:PMC7356850
doi:10.3390/plants9060732
PMID:32532006
The Potential Therapeutic Value of Medicinal Plants in the Management of Metabolic Disorders Nyakudya TT, Tshabalala T, Dangarembizi R, Erlwanger KH, Ndhlala AR Molecules 09-Jun-2020
PMCID:PMC7321241
doi:10.3390/molecules25112669
PMID:32526850
An Overview of the Potential Use of Ethno-Medicinal Plants Targeting the Renin–Angiotensin System in the Treatment of Hypertension De Lange-Jacobs P, Shaikh-Kader A, Thomas B, Nyakudya TT Molecules 30-Apr-2020
PMCID:PMC7249071
doi:10.3390/molecules25092114
PMID:32366012
Exploring a New Natural Treating Agent for Primary Hypertension: Recent Findings and Forthcoming Perspectives Lin SR, Lin SY, Chen CC, Fu YS, Weng CF J Clin Med 16-Nov-2019
PMCID:PMC6912567
doi:10.3390/jcm8112003
PMID:31744165
A comprehensive review on beneficial dietary phytochemicals in common traditional Southern African leafy vegetables Sivakumar D, Chen L, Sultanbawa Y Food Sci Nutr 14-Apr-2018
PMCID:PMC6021739
doi:10.1002/fsn3.643
PMID:29983933
Evolutionary routes to biochemical innovation revealed by integrative analysis of a plant-defense related specialized metabolic pathway Moghe GD, Leong BJ, Hurney SM, Daniel Jones A, Last RL eLife 30-Aug-2017
PMCID:PMC5595436
doi:10.7554/eLife.28468
PMID:28853706
Genetic diversity and population structure in Physalis peruviana and related taxa based on InDels and SNPs derived from COSII and IRG markers Garzón-Martínez GA, Osorio-Guarín JA, Delgadillo-Durán P, Mayorga F, Enciso-Rodríguez FE, Landsman D, Mariño-Ramírez L, Barrero LS Plant Gene 01-Dec-2015
PMCID:PMC4630809
doi:10.1016/j.plgene.2015.09.003
PMID:26550601
Physalis alkekengi Carotenoidic Extract Inhibitor of Soybean Lipoxygenase-1 Activity Chedea VS, Pintea A, Bunea A, Braicu C, Stanila A, Socaciu C Biomed Res Int 09-Jan-2014
PMCID:PMC3910512
doi:10.1155/2014/589168
PMID:24511537

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 / Hasubanan alkaloids
(1S,8S,10S,11R,12R)-3,4,11,12-tetramethoxy-17-methyl-18-oxa-17-azapentacyclo[8.4.3.18,11.01,10.02,7]octadeca-2(7),3,5-trien-13-one 21769000 Click to see CN1CCC23C14CC(C5=C2C(=C(C=C5)OC)OC)OC4(C(C(=O)C3)OC)OC 389.40 unknown https://doi.org/10.1007/BF00579065
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3R,4S,5R,6R)-2-[(2R,3R,4R,5S)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3-methylbut-2-enoyloxy)oxan-3-yl] dodecanoate 21575480 Click to see CCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)CO)O)O)CO)CO)O)OC(=O)C=C(C)C 606.70 unknown https://doi.org/10.1021/NP049746R
[2-[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3-methylbut-2-enoyloxy)oxan-3-yl] dodecanoate 73101229 Click to see CCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)CO)O)O)CO)CO)O)OC(=O)C=C(C)C 606.70 unknown https://doi.org/10.1021/NP049746R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(1S,2R,6S,7R,9R,11S,12S,15S,16S)-15-acetyl-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 132607780 Click to see CC(=O)C1CCC2C1(CCC3C2CC4C5(C3(C(=O)C=CC5O)C)O4)C 344.40 unknown https://doi.org/10.1016/0031-9422(93)85379-6
15-Acetyl-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 162927021 Click to see CC(=O)C1CCC2C1(CCC3C2CC4C5(C3(C(=O)C=CC5O)C)O4)C 344.40 unknown https://doi.org/10.1016/0031-9422(93)85379-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1R,2R,6S,7R,9R,11R,12R,15S,16R)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-6,12,15-trihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 162939343 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C 502.60 unknown https://doi.org/10.1007/BF00634733
(1R,2R,6S,7R,9R,11S,12R,15S,16S)-6,12,15-trihydroxy-15-[(1S)-1-hydroxy-1-[(2S)-4-(hydroxymethyl)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 162988759 Click to see CC1=C(CC(OC1=O)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)CO 518.60 unknown https://doi.org/10.1007/BF00579065
(1S,2R,4R,6R,7S,8R,10R,12S,13S,16R,17S)-7-hydroxy-16-[(1S)-1-[(2S)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,17-dimethyl-5,9-dioxahexacyclo[10.7.0.02,8.04,6.08,10.013,17]nonadecan-3-one 162934435 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C7C(C6O)O7)C)O5)C)CO 486.60 unknown https://doi.org/10.3987/S-1981-01-0317
(1S,2R,5S,6S,7R,9R,11S,12S,15R,16S)-5,6-dihydroxy-15-[(1S)-1-[(2S)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162929032 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O)C)O5)C)CO 488.60 unknown https://doi.org/10.3987/S-1981-01-0317
(1S,2R,6S,7R,9R,11R,12R,15S,16S)-15-[(1S)-1-[(2S)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-6,12,15-trihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 156017944 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6
(2R)-2-[(1S)-1-hydroxy-1-[(4S,5S,9S,10R,13S,17S)-4,5,17-trihydroxy-10,13-dimethyl-1-oxo-4,6,7,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 163195107 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3=C4CCC5(C(C=CC(=O)C5(C4CCC32C)C)O)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00638778
(2R)-2-[(1S)-1-hydroxy-1-[(6S,8R,9S,10R,13S,14R,17S)-6,14,17-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 127047502 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC(C5=CC=CC(=O)C45C)O)C)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00579065
(2R)-4-(hydroxymethyl)-2-[(1S)-1-hydroxy-1-[(4S,8R,9S,10R,13S,14R,17S)-4,14,17-trihydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-methyl-2,3-dihydropyran-6-one 21607596 Click to see CC1=C(CC(OC1=O)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)O)CO 502.60 unknown https://doi.org/10.1007/BF00579480
(2R)-4-(hydroxymethyl)-2-[(1S)-1-hydroxy-1-[(6R,8R,9R,10R,13S,14R,17S)-6,14,17-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-5-methyl-2,3-dihydropyran-6-one 162857209 Click to see CC1=C(CC(OC1=O)C(C)(C2(CCC3(C2(CCC4C3CC(C5=CC=CC(=O)C45C)O)C)O)O)O)CO 502.60 unknown https://doi.org/10.1007/BF00579065
(2S)-2-[(1S)-1-hydroxy-1-[(6R,8R,9S,10R,13S,14R,17S)-6,14,17-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl]ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 162880001 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC(C5=CC=CC(=O)C45C)O)C)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00579065
(8R,9R,10R,13R,14R,17S)-17-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-14,17-dihydroxy-10,13-dimethyl-3,7,8,9,11,12,15,16-octahydro-2H-cyclopenta[a]phenanthrene-1,4-dione 162845519 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5=O)C)C)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00634733
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one 301754 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)C 470.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6
15-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-6,12,15-trihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-3-one 3836120 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C 502.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6
https://doi.org/10.1007/BF00634733
17-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-14,17-dihydroxy-10,13-dimethyl-3,7,8,9,11,12,15,16-octahydro-2H-cyclopenta[a]phenanthrene-1,4-dione 73800703 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)CCC5=O)C)C)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00634733
2-[1-Hydroxy-1-(4,14,17-trihydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 73800702 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)O)C 486.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6
2-[1-Hydroxy-1-(4,5,17-trihydroxy-10,13-dimethyl-1-oxo-4,6,7,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 74039536 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3=C4CCC5(C(C=CC(=O)C5(C4CCC32C)C)O)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00638778
https://doi.org/10.1016/0031-9422(93)85379-6
2-[1-Hydroxy-1-(6,14,17-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)ethyl]-4,5-dimethyl-2,3-dihydropyran-6-one 14860927 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC(C5=CC=CC(=O)C45C)O)C)O)O)O)C 486.60 unknown https://doi.org/10.1007/BF00579065
4-(Hydroxymethyl)-2-[1-hydroxy-1-(4,14,17-trihydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)ethyl]-5-methyl-2,3-dihydropyran-6-one 73800700 Click to see CC1=C(CC(OC1=O)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)O)CO 502.60 unknown https://doi.org/10.1007/BF00579480
4-(Hydroxymethyl)-2-[1-hydroxy-1-(6,14,17-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-17-yl)ethyl]-5-methyl-2,3-dihydropyran-6-one 73833824 Click to see CC1=C(CC(OC1=O)C(C)(C2(CCC3(C2(CCC4C3CC(C5=CC=CC(=O)C45C)O)C)O)O)O)CO 502.60 unknown https://doi.org/10.1007/BF00579065
4beta-Hydroxywithanolide E 73621 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C 502.60 unknown https://doi.org/10.1007/BF00634733
https://doi.org/10.1016/0031-9422(93)85379-6
5,6-Dihydroxy-15-[1-[5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 72835871 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O)C)O5)C)CO 488.60 unknown https://doi.org/10.3987/S-1981-01-0317
7-Hydroxy-16-[1-[5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,17-dimethyl-5,9-dioxahexacyclo[10.7.0.02,8.04,6.08,10.013,17]nonadecan-3-one 162934434 Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C7C(C6O)O7)C)O5)C)CO 486.60 unknown https://doi.org/10.3987/S-1981-01-0317
Physapruin A 21607598 Click to see CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5O)C)C)O)O)O)C 486.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6
Withanolide D 161671 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)C 470.60 unknown https://doi.org/10.1016/0031-9422(93)85379-6

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