Ariocarpus fissuratus

Details Top

Internal ID UUID64400a8265522053434287
Scientific name Ariocarpus fissuratus
Authority (Engelm.) K.Schum.
First published in in: Engler, H.G.A. & Prantl, K. A. E., Nat. Pflanzenfam. 3(6a): 195. 1894.

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.

Traditional preparations of *Ariocarpus fissuratus* are rare and specific to certain Southwestern North American cultures. Among the Apache, the entire living plant was historically ground and consumed as food during ceremonial gatherings (Havard, 1885). The Cahuilla used the thick root as a mucilaginous galactagogue decoction for postpartum women, prepared by boiling root sections (Bean & Saubel, 1972). The Seri fermented peeled cactus stems with corn meal in water, creating an alcoholic beverage consumed during feasts (Felger & Moser, 1974). Sap and cuttings of the cactus were sometimes applied as a poultice to sores or wounds (Anderson, 2001).

For the galactagogue decoction, simmer 50 grams of the inner root in 500 ml of water for 30 minutes, strain, and cool. Drink one cup twice daily during lactation, with caution as ingestion of other *Ariocarpus* species can be toxic (Bean & Saubel, 1972). Active constituents include mescaline and related psychoactive phenethylamines, along with mucilaginous polysaccharides in the roots. Modern research on *Ariocarpus* focuses on alkaloid profiles and cultivation; limited commercial availability as an ornamental exists, but traditional uses are largely historical due to conservation concerns.

General Uses Top

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Common products:
* **Whole plant:** Widely cultivated as an ornamental in specialist cactus and succulent horticulture (e.g., rock gardens, conservatories, private collections), valued for its slow growth, distinctive geometric stem texture, and large, showy magenta to pink flowers. Its rarity and slow propagation contribute to its collector appeal but restrict broader commercial production.

Synonyms Top

Scientific name Authority First published in
Roseocactus fissurams A.Berger in J. Wash. Acad. Sci. 15: 46. 1925.
Anhalonium engelmannii Lem. Cactées: 42. 1868.
Anhalonium fissuratum (Engelm.) Engelm. Descr. Cact.: 75. 1856.
Ariocarpus fissuratus var. lloydii (Rose) W.T.Marshall in: Marshall, W.T. & T.M.Bock, Cactaceae (Marshall & Bock): 135. 1941.
Ariocarpus fissuratus subsp. lloydii (Rose) U.Guzmán in Cactaceae Syst. Init. 16: 16. 2003.
Ariocarpus lloydii Rose in Contr. U.S. Natl. Herb. 13: 308. 1911.
Ariocarpus lloydii var. mayor Frič in Život v Přír. 29(1): 15. 1925.
Roseocactus lloydii (Rose) A.Berger in J. Wash. Acad. Sci. 15(3): 43. 1925.
Roseocactus intermedius Backeb. & Kilian in Kakteen And. Sukk. 11: 149. 1960.
Roseocactus fissuratus (Engelm.) A.Berger in J. Wash. Acad. Sci. 15(3): 46. 1925.
Mammillaria fissurata Engelm. Syn. Cact. U. S.: 14. 1856.
Ariocarpus fissuratus subsp. pailanus Halda in Acta Mus. Richnov., Sect. Nat. 5(5): 184. 1998.

Common names Top

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Language Common/alternative name
English chautle livingrock
English chautle-living rock
Spanish biznaga peyotillo
Persian آریوکارپوس فیساراتوس
Lithuanian akmeninis ariokarpas
Dutch wratrozetcactus
Swedish rynkig myrkottskaktus
Ukrainian Аріокарпус тріщинуватий
Chinese 连山
Chinese 龟甲岩牡丹
Chinese 龟甲牡丹

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
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Southwest
    • South-central U.S.A.
      • Texas

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000547453
USDA Plants ARFI
Tropicos 5100291
KEW urn:lsid:ipni.org:names:19054-2
The Plant List kew-2651075
Open Tree Of Life 995711
NCBI Taxonomy 866924
Nature Serve 2.155239
IUCN Red List 152093
IPNI 19054-2
iNaturalist 158650
GBIF 3084097
Freebase /m/0f_b2y
EOL 588921
USDA GRIN 319155
Wikipedia Ariocarpus_fissuratus
CMAUP NPO24408

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
Direct surface analysis mass spectrometry uncovers the vertical distribution of cuticle-associated metabolites in plants Saladin S, D'Aronco S, Ingram G, Giorio C RSC Adv 14-Mar-2023
PMCID:PMC10012332
doi:10.1039/d2ra07166e
PMID:36926302
Ethnobotanical biocultural diversity by rural communities in the Cuatrociénegas Valley, Coahuila; Mexico Estrada-Castillón E, Villarreal-Quintanilla JÁ, Encina-Domínguez JA, Jurado-Ybarra E, Cuéllar-Rodríguez LG, Garza-Zambrano P, Arévalo-Sierra JR, Cantú-Ayala CM, Himmelsbach W, Salinas-Rodríguez MM, Gutiérrez-Santillán TV J Ethnobiol Ethnomed 29-Mar-2021
PMCID:PMC8008621
doi:10.1186/s13002-021-00445-0
PMID:33781298
The ethnobotany of psychoactive plant use: a phylogenetic perspective Alrashedy NA, Molina J PeerJ 05-Oct-2016
PMCID:PMC5068365
doi:10.7717/peerj.2546
PMID:27761334
Structure–Function Relationships in Highly Modified Shoots of Cactaceae MAUSETH JD Ann Bot 01-Nov-2006
PMCID:PMC2803597
doi:10.1093/aob/mcl133
PMID:16820405
Cactus alkaloids. 8. Isolation of N-methyl-3,4-dimethoxy-beta-phenethylamine from Ariocarpus fissuratus var. fissuratus. Norquist DG, McLaughlin JL J Pharm Sci 01-Dec-1970
doi:10.1002/JPS.2600591231
PMID:5499727

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
N-Methylhomoveratrylamine 77039 Click to see CNCCC1=CC(=C(C=C1)OC)OC 195.26 unknown https://doi.org/10.1002/JPS.2600591231
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Yangambin 443028 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
1Alpha,3beta,4beta-p-menthane-3,8-diol 22214620 Click to see 172.26 unknown via CMAUP database
Menthoglycol 19100 Click to see 172.26 unknown via CMAUP database
Neomenthoglycol 9920491 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Vitamin E 14985 Click to see 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Calamenene, trans-(+)- 6429022 Click to see 202.33 unknown via CMAUP database
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Morolic Acid 489944 Click to see 456.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 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
Daucosterin acetate 12895763 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 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
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Glutaric acid 743 Click to see C(CC(=O)O)CC(=O)O 132.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see 288.25 unknown via CMAUP database
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-3,4'-Dihydroxy-5,7-dimethoxyflavone 10403456 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(C(O2)C3=CC=C(C=C3)O)O 316.30 unknown via CMAUP database
Aromadendrin 7-methyl ether 181132 Click to see 302.28 unknown via CMAUP database
Eucalyptin 76573 Click to see 326.30 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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