Gymnocalyciums

 This section details only those gymnocalyciums that have been reported to contain mescaline. A more comprehensive treatment of the analytical accounts of the entire genus can be located within Cactus Chemistry By Species_2014_Light which also includes the analytical results listed below.
Some synonyms are included but in most cases the names have been left however they were analyzed as the lumping resulting from the mergers help to obscure some interesting chemistry. These are not being kept separated as an suggestion that they merit recognition, this practice is being employed simply to better preserve and illustrate the published chemical variances. Synonyms are also included so this should be found more helpful than not. Similarly in those analysis involving invalid names, the abandoned names are preserved a,s while those names may be invalid, the analytical results are meaningful as they actually analyzed horticultural plants that physically exist whether they have a good name or not.

 

Gymnocalycium species

 

Gymnocalyciums: Gymnocalycium fleisheranum

Gymnocalycium fleisheranum

 

Commonly called “Chin Cactus” due to the “chin” below each areole.
See examples above and below.

 

Gymnocalyciums: Gymnocalycium triacanthum

Gymnocalycium triacanthum

 

Fruit are typically oblong and red (see image at top of page).
Hortus Third. page 530.

Name is from the Greek:
gymnos “bare” and kalyx “bud”; for its bare flower buds.

 

Gymnocalyciums: Gymnocalycium triacanthum

Gymnocalycium triacanthum

 

See also Backeberg 1959 [3: 1695-1786] (includes many pictures.) and Britton & Rose 1922 [3: 152-166] (includes a number of pictures).

 

Only a representative sampling of the species listed have entries below.

 

Gymnocalyciums: Gymnocalycium asterium

Gymnocalycium asterium

 

A simple list of the mescaline containing Gymnos:

 Gymnocalycium achirasense Till. & Schatzl

 Gymnocalycium asterium Ito (now merged into G. stellatum)

 [Available varieties include:

     v. albispinum

     v. nigrispinum

     v. paucispinum

     v. roseiflorum]

 Gymnocalycium baldianum (Speg.) Spegazzini

 Gymnocalycium calochlorum (Bödeker) Y. Ito

 Gymnocalycium carminanthum Borth & Koop

     [var. minimum is also available.]

 Gymnocalycium comarapense Backeberg

 Gymnocalycium denudatum (L.&O.) Pfeiff.

 Gymnocalycium fleischerianum Backeberg (No reference was included)

 Gymnocalycium gibbosum (Haworth) Pfeiffer

 Gymnocalycium horridispinum Frank

 Gymnocalycium leeanum (Hook.) Britton & Rose

 Gymnocalycium mesopotamicum Kiessling

 Gymnocalycium monvillei (Lemaire) Br. & R.

 Gymnocalycium moserianum Schutz

          [var. laejera is also available.]

 Gymnocalycium netrelianum (Monville) Br. & R.

 Gymnocalycium nigriareolatum Backeberg

 Gymnocalycium oenanthemum Backeberg

 Gymnocalycium paraguayense Schutz

 Gymnocalycium quehlianum (Haage) Berger

   Available varieties include:

     v. albispinum

     v. flavispinus

     v. kleinianum

     v. nigrispinum

 Gymnocalycium ragonesii Castellano

 Gymnocalycium riojense Fric ex. H.Till. & W.Till 

 Gymnocalycium riograndense Cardeñas (now Gymnocalycium pflanzii subsp. zegarrae)

 Gymnocalycium stellatum Spegazzini

 Gymnocalycium striglianum Jeggle

 Gymnocalycium triacanthum Backeberg

 Gymnocalycium uebelmannianum Rausch

 Gymnocalycium valnicekianum Jajó (now Gymnocalycium mostii subsp. valnicekianum)

 Gymnocalycium vatteri Buining (now Gymnocalycium ochoterenae subsp. vatteri)

 

 A summary of the published chemistry can be found at the end of the Gymnocalycium examples below.

 

A handful of Gymnocalycium species:

 

Gymnocalycium baldianum  (Spegazzini) Spegazzini

Carlo Luigi Spegazzini (1905) Anales del Museo Nacional de Buenos Aires. Buenos Aires, ser. 2,  3, 4: 505. as Echinocactus baldianus.
Carlo Luigi Spegazzini (1925) Anales de la Sociedad Cientifica Argentina, 99: 135. as Gymnocalycium baldianum.

 

Gymnocalyciums Gymnocalycium baldianum

Gymnocalycium baldianum

 

Small amounts of mescaline reported.

Origin: Argentina (Andalgalá (mountains east of), Catamarca, Cuesta de Portezuelo, Cuesta de Totoral,Hualfin, Sierra Ancasti,Sierra Graciana, Sierra de Guayamba, Sierra de Narvaes, Sierra de Manchao) Collections have been reported from (500m-)900m-1700m(-2000m)

 Habitat: Among grasses. (IUCN citing Charles 2009)

86. Echinocactus Baldianus Speg. (n. sp.)

Diag. Hybocactus, parvus globoso -depressus, obscure snbcinerascente-viridis; costis 9-11 latis et obtusissimis, sulco acuto profundiusculo limitatis, fere in tuberculis solutis; areolis parvis: aculéis gracilibus saepius 5, ómnibus marginalibus radiantibus adpressis sordide pallideque ciñereis; floribus apicalibus erectis mediocribus extus obscure glauco-viridibus glaberrimis laxe squamosis, squamis sensim in phylla intense purpurea transeuntibis, laciniis stigmaticis brevibus 6 albo-ochroleucis. Speggazini 1905

Depressed-spherical body, to 7 cm in diameter and 10 cm tall. [Eventually to 3.5 inches in diameter; Anderson 1998]
Epidermis is dark greyish to bluish-green.
9-11 ribs, fewer at first, becoming more distinctly tuberculate.
5-7 pinkish-grey to horn-grey or ash-grey, radial spines. More or less appressed or directed laterally, somewhat darker below at first. Spines are weak and flexible; sometimes twisting.
No centrals.
[1.5 inch wide] flowers are variable; lighter or darker red to a more or less blood-red. [White, pink, orange, red or shades in between; borne in spring.
Flowering can occur for several months. Anderson 1998] Pilbeam notes flowers to be variable as pink through red but proposes that hybridization may be responsible for some of the color forms.
Flowers around Christmas in habitat.
Bears dark green elongated fruit.
Backeberg 1977: page 183.
Pilbeam 1995: pages 43-44,  fig 14.

Photos with flower: Anderson 1998: page 80 & Pilbeam 1995: plate 15.

Anderson 1998 claims flowering size (1.5 inches in diameter) can be reached in 12 months from seed and it will handle 10°F briefly.

Listed by IUCN as “Least Concern” as, despite a restricted range and pressure from collection activity, it has a continuous range. Local collection and fire are said to be the primary threats.
Perea, M. & Trevisson, M. 2013. Gymnocalycium baldianum. The IUCN Red List of Threatened Species. Version 2014.2. <www.iucnredlist.org>

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

Gymnocalycium calochlorum  (Bödeker) Y.Itô

Friedrich Bödeker (1932) Monatsschrift der Deutschen Kakteen-Gesellschaft, 4: 260. as Echinocactus calochlorus.
Yoshi Itô in John Borg  (1952) Cacti, 90. as Gymnocalycium calochlorum.

 

Gymnocalyciums: Gymnocalycium calochlorum

Gymnocalycium calochlorum

 

Small amounts of mescaline reported.

Origin: Argentina (The original collection did not include a locality. Reported to occur at Cordoba, Nono, Villa Bura Borchero, La Mudana, Las Rabonas. Collections have been recorded from 900 and 1000m according to Pilbeam; 800-1500m according to IUCN.)

Habitat:  “often buried in crumbling granite, where it can be difficult to find if not in flower or fruit (Charles 2009). It grows in high-altitude grasslands and chaco forest.” IUCN

Cushion forming plant with depressed-spherical cushion-like single heads.
Bodies are grey-green to blue-green to around 6 cm diameter and to 4 cm high.
Around 11 tuberculate ribs with creamy-white felted round areoles.
Up to 9 closely set whitish to pale pinkish-brown radial spines that are thin, wispy, rough, appressed, more or less curving; to 9(-12.5) mm long. No centrals.
Pale pink flowers to 6 cm long, opening only moderately. Produced only from the youngest areoles. Petals are not revolute.
Floral tube is long and of a lighter green according to Backeberg or bluish according to Pilbeam.
Fruit is bluish-green and long-ovoid.
Backeberg 1977 page 184,
and Pilbeam 1995: pages 52-53, Photos as fig. 21 and plates 25 (flowering) & 26 (in habitat),
and Pizzetti 1985 entry #117 (includes picture)

Listed by the IUCN as a species of “Least Concern” due to a perception of it being locally abundant and resistant to disturbances.  The IUCN says both “It is very widespread…” and  “…the range is not particularly wide,…”
Demaio, P. & Trevisson, M. 2013. Gymnocalycium calochlorum. The IUCN Red List of Threatened Species. Version 2014.2.

 

Gymnocalyciums: Gymnocalycium calochlorum

Gymnocalycium calochlorum

 

Recognized varieties mentioned by Pizzetti (only the first is respected by Pilbeam):
 var. proliferum; with larger darker or glacous stems, flowers that open widely and flower segments that curve outward (may be
brownish-white, pink or white; often pink at base.)

 var. roseiacanthum; a smaller variety (half the size of the
species). Glaucous green with yellowish rounded areoles and contorted
pinkish spines. Flowers are large and white with red bases. These
plants occur in the Sierra de Córdoba.

Pizzetti recommends protection from intense cold and shady positions when the sun is hottest. Prefers cool weather.

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

Gymnocalycium gibbosum (Haworth) Pfeiffer

Adrian Hardy Haworth (1816) Botanical Register; 2: 137. as Cactus gibbosus.
Louis Pfeiffer ex Ludwig Mittler (1844) Taschenbuch für Cactusliebhaber. Leipzig, 2: 124. as Gymnocalycium gibbosum.

 

Gymnocalyciums: Gymnocalycium gibbosum

Gymnocalycium gibbosum

 

Presence of mescaline reported but unconfirmed.

Origin: Southern Argentina. [Río Chubut, Río Negro and Chubul Provinces:
Lat. 40-45o S.; La Plata, Mendoza, San Luis] 

Pilbeam 1995 mentions the species as being widespread in Argentina “covering a great deal of Patagonia, the provinces La Pampa and Buenos Aires and as far west as Mendoza and reported from southern Argenia, at Chubut, Rio Negro and Santa Cruz; recently by Pilz from Argentina, Abra de la Ventura.” Collections have been reported from 400-500m.
The IUCN cites Hunt et al. 2006 as giving occurrences “at elevations of 0 to 1,000 m“.

Habitat:monte shrubland and patagonian steppe (estepa patagónica)” “likes the sandy or gravelly alluvial soil along the Río Negro and Río Colorado, where it grows under bushes and other plants (Charles 2009).” IUCN

gymnocalyciums: Haworth 1816 BotanicalRegister, 137, diagnosis of Cactus gibbosus

Haworth 1816 Botanical Register, 2: 137, Latin diagnosis of Cactus gibbosus

Solitary glaucous, dull or dark (bluish)green well-armed stems, (Pilbeam: dark green to blue-black or greyish-green”) later sooty or brownish-green, to 10 [-24] inches (12-15 cm) high and 6 inches (10-12 cm) thick. Starts
globular then becomes more cylindrical.

Areoles set 1.5-2 cm apart.
12-14 [-19] strongly tubercled, straight, notched and rounded ribs with lightly sunken round areoles with greyish (Pilbeam describes as brownish-cream) wool. Prominent chins below areoles. 
7-12 radial spines, stiff, spreading, needle-shaped to awl-shaped, typically straight but  may be slightly curved, and mostly brown. (or light brown with a reddish base.) Up to 3.5 cm long. Nearly spineless at apex.
Can have 1-3 central spines (0-6 according to Pilbeam) but usually they are absent. When present they are often not readily distinguishable from the radial spines.
White (to faintly pink or reddish) flowers to 2-1/2 [to 2-3/4] inches long (6 cm long opening to 6 cm wide). Inner petals are lanceolate. Petals shaded from white to pink. Stamens and stigma are white; stigma has 12 yellowish lobes.
Diurnal flowers in summer.
Produced a club-shaped short, dark-green fruit.
Seldom branches unless injured or grafted, but some varieties do branch freely.
page 530 in Hortus Third
and Backeberg 1977: page 186
and Borg 1937: page 239
and Innes & Glass 1991: page 127 [Includes
picture of flowers]

and Lamb & Lamb 1971: page 654
and Pilbeam 1995: pages 73-76, fig. 37 & 38, plate 47
and Pizzetti 1985 Entry #119. (has color photo)


Listed by IUCN as a species of “Least Concern” due to having no major threats and having a wide range in which it occurs abundantly.   ListedIts range includes protected areas.
Demaio, P. & Trevisson, M. 2013. Gymnocalycium gibbosum. The IUCN Red List of Threatened Species. Version 2014.2.

 

Gymnocalyciums: Gymnocalycium gibbosum

Gymnocalycium gibbosum

Hortus recognizes:
 cv. Ferox has more numerous spines

 cv. Nigrum has very dark spines

 cv. Schlumbergii has more numerous spines that are stiff pinkish red to amber yellow.

     page 530 in Hortus Third

 

Gymnocalyciums: Gymnocalycium gibbosum var. schlumbergii

Gymnocalycium gibbosum cv. Schlumbergii

 

Many varieties exist in both the wild and in cultivation. First described in 1812. Has been known by many names over the years due to its varieties.
 Entry #119 in Pizzetti 1985

Pilbeam 1995 mentioned that “Nearly 30 varietal names have been allocated to this species.”

 cv. Nobile is said to have a larger sperical stem and longer overlapping spines; white with red base.

 Borg 1977 mentions var. caespitosum Hort., var. ferox Lab., var. leucacanthum K.Schum., var. Schlumbergeri K.Schum., var. nobilis K.Schum., and var. leonensis Hildm.

 Backeberg 1977 mentions var. leucodictylon (K.Schum.) Y.Ito, var. nigrum Backbg, and var. nobile (Haw.) Y.Ito.

 var. rostratum is also commercially available. It is described as having a dark grey stem.

IPNI lists:

v. borthii

v. brachypetalum

f. cerebriforme

var cerebriformis

var. chubutense

ssp ferdinandii

ssp. ferox

ssp. gastonii

var. nigrum

ssp. radekii

ssp. radovanii

This has always been a popular plant and is widely grown.

Innes & Glass recommend indirect light and a 50°F minimum temperature.
Pizzetti describes it as cold tolerant but taking no frost, tolerant of heat and requiring some sun.
I’ve found it to be able to survive frost but typically scarring badly afterwards. In Texas,  it was repeatedly attacked by thrips.

[See also Backeberg 1959 [3: 1752-1755] (includes pictures of several varieties, also fig. 1687, page 1756 and fig. 1688, page 1757.) and Backeberg 1977 page 186 and Britton & Rose 1922 [3: 158-159] (picture in fig. 166 page 157.]

 

Reported analysis:

92.1% water by weight (pH of juice: 4.6-5) Herrero-Ducloux 1930b

 Mescaline, Anhalamine & Lophophorine

 (all identified by chemical tests)
Mata & McLaughlin 1982 cited Herrero-Ducloux 1930b and Reti 1950 (who also cited Herrero-Ducloux)

 [Ott 1993, page 114, cites Der Marderosian 1966; mentioning this is a simple listing of mescaline species, rather than a primary source.]

 Štarha et al. 1997 did not observe mescaline to be present. See the alkaloid list further below.

Reti 1950 and Chemical Abstracts 1930 says that Enrique Herrero-Ducloux 1930b isolated small amounts of alkaloids from this cactus which he noted gave chemical reactions similar to those of mescaline [Colorless birefringent crystals, n 1.544, mp 160-162°], and what he thought was probably a mixture of anhalonine and lophophorine [Colorless birefringent crystals, n 1.552, mp 188-190°].

No definitive proof was done and apparently only Dr. Štarha has cared enough to follow through during the 70 years which have passed.

 

Gymnocalyciums: Gymnocalycium gibbosum

Gymnocalycium gibbosum

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

 

 

 Gymnocalycium leeanum (Hooker) Britton & Rose

William Jackson Hooker (1845) Botanical Magazine; or, Flower-Garden Displayed…, 71: t. 4184, as Echinocactus leeanus
Nathaniel Lord Britton & Joseph Nelson Rose (1922) Cactaceae, 3: 154, fig. 164, as Gymnocalycium leeanum
Wolfgang Papsch (2000) Gymnocalycium, 13 (3): 371. as Gymnocalycium reductum var. leeanum

 

Gymnocalyciums: Gymnocalycium-leeanum-HBG

Gymnocalycium leeanum

Presence of mescaline reported but unconfirmed.

Origin: Argentina and Uruguay

Habitat: Grasslands in rocky places and on hills. Also in organic materials among rocks. Sometimes under shrubs.  IUCN citing Charles 1009.

Echinocactus Leeanus: depresso-globosus obscure subglauco-v i r i d i s tuberculis subhemisphaericis majusculis obtuse hexahedris mammiformibus confluentibus, in series irregulares subverticales dispositis, areolis ovalibus tomentosis, aculeis subgracilibus quorum subdecem patentibus rectiusculis cum unieo centrali porrecta v i x majore, floribus majusculis pallide flavescentibus. (Hooker 1845)

Bluish-green stems ~3 inches thick. Depressed to spherical. [“rather flattened” Innes & Glass]
~16 ribs, irregular, strongly tubercled (more or less six-sided)
Radial spines about 7-10(-11) needle-shaped, thin, appressed, 1/2 inch long.
Central spine 1 straight and directed outward. Not always present.
Flowers pale yellow [“yellowish-white, 2-2½ in long and high” Innes & Glass] to 2 inches (unisexual).
Blooms in early summer.
Backeberg 1959 [3, pages 1735-1737, (includes pictures of two varieties.)
and Backeberg 1977: page 188
and Britton & Rose 1922: page 154 (picture in fig. 164, page 156)
and Hortus Third: page 530.
and Innes & Glass 1991: page 128 (includes picture of species and var. netrelianum, both with flower)

[Schuster 1990 has photo on p. 128.] 

 var. brevispinum Backeberg is described from Maldonado, Uruguay. It is said to have much shorter and straighter spines.

var. netrelianum (Monv.) Backeb, (= G. netrelianum (Monv.) Britt. and Rose Hortus Third Page 530. [see entry of G. netrelium]) Backeberg lists separately; G. leeanum var. netrelianum (Uruguay): tubercle said to be broader than high, spines longer [5-8, centrals absent; Backeberg 1977].

 Innes & Glass describe var. netrelianum as being slightly more globular with fewer, shorter spines (5-7), usually no centrals and having citron yellow flowers 1.5 to 1.75 inches in diameter.

Listed by IUCN as a species of “Least Concern” due to having a fairly wide range that includes protected areas. Its major threats appear to be from human activity and grazing.
Kiesling, R. 2013. Gymnocalycium reductum. The IUCN Red List of Threatened Species. Version 2014.2. www.iucnredlist.org.

Innes & Glass recommend slight shade and a minimum of 50°F.

 

Reported chemistry of Gymnocalycium leeanum:

 Tyramine (gc),

 N-Methyl-tyramine (gc),

 Hordenine (ms, gc),

 Mescaline (chemical tests; unconfirmed),

 Anhalonine (chemical tests)

 and Lophophorine (chemical tests)

     Mata & McLaughlin 1982 citing DeVries et al. 1971 and Herrero-Ducloux 1930b (Apparently DeVries and coworkerrs did not find mescaline, finding the first three phenethylamines instead.
The UT library is missing the first several issues of both journals. It is unknown to me what variety either DeVries or Herrero-Ducloux used or whether this was either noted or even taken into account.)

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

 

 

 Gymnocalycium multiflorum (Hooker) Britton & Rose

William Jackson Hooker (1845) Curtis‘ Botanical Magazine, 71: t. 4181, as Echinocactus multiflorus.
Nathaniel Lord Britton & Joseph Nelson Rose (1918) Addisonia, 3: 5, pl. 83, as Gymnocalycium leeanum.
[Now considered lumped as a synonym with Gymnocalycium monvillei
i.e. Nathaniel Lord Britton & Joseph Nelson Rose (1922) Cactaceae, 3: 161, as Gymnocalycium monvillei Pfeiff. ex Britton & Rose.]

 

Gymnocalyciums: Gymnocalycium-multiflorum-flower

Gymnocalycium multiflorum

Gymnocalycium: Gymnocalycium multiflorum Hooker 1845

gymnocalyciums; Gymnocalycium multiflorum Latin diagnosis

 

Herrero-Ducloux 1932a reported recovering small quantities of a ‘mescaline-like’ alkaloid from this species. Reti notes as occuring in Cordoba and Catamarca in Argentina, also in Brazil, Uruguay and Paraguay.
This species is fairly frequent in cactus collections and is readily available commercially. It is one of the more easily
recognizable Gymnocalycium species.

  This report is unconfirmed as it apparently lacks any further work. This species is regarded to be a synonym of Gymnocalycium monvillei which HAS been reported to contain mescaline. See more details under that name.

 

Gymnocalyciums: Gymnocalycium multiflorum

Gymnocalycium multiflorum

 

  G. monvillei is listed as being a species of “Least Concern” by the IUCN.
Demaio, P., Lowry, M., Trevisson, M. & Méndez, E. 2013. Gymnocalycium monvillei. The IUCN Red List of Threatened Species. Version 2014.2. <www.iucnredlist.org>. 

 

External resources:

Gymnocalycium.free.fr

 

 

 Gymnocalycium riograndense Cardeñas

Martin Cárdenas (1958) Kakteen und Andere Sukkulenten, 9: 24, as Gymnocalycium riograndense.
Graham Charles (2005) Cactaceae Systematics Initiatives: Bulletin of the International Cactaceae Systematics Group, 20: 18, as Gymnocalycium pflanzii subsp. zegarrae .

 

Gymnocalyciums: Gymnocalycium-riograndense

Gymnocalycium riograndense

 

Mescaline reported in small amounts.

Origin: Bolivia. Along Rio Grande “between the Cordillera de Cochabamba and the plano of the Rio Guarayos”. Pizzetti 1985.

Habitat: (As G. pflanzi) growing in deep rich soils in sunny rocky areas on slopes or under spiny shrubs. Cactus-Art.

Plants broadly spherical, to 6 cm high, to 20 cm diameter [2-1/2 inches tall and up to 8 inches in diameter]. Initially remaining simple but offshooting from base as adults.
Body is glossy, dark green. [The plant in Pizzeti’s photo is not dark]
Around 13 ribs, to 3 cm wide; Tubercles are obtusely conical, separated by transverse dividing lines; a slender conical beak is below the tubercles.
Round areoles covered with white felt when young but later becoming bare.
8(-9) thin-subulate radial spines, to 2.5 cm long; slightly curving.
They are stiff, grey, black-tipped, brownish below. Later becoming brown all over.
No centrals.
Beaker-shaped flowers are white, with a bluish-red throat.
Backeberg 1977 page 193
and Pizzetti 1985 Entry #126 (Has picture.)

Pizzetti recommends mild winter heat.

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

 

 

 Gymnocalycium valnicekianum Jajó

Bedrich Jajó (1934) Kaktusář; odborný měsičnik. Astrophytum spolek pestitelu kaktusu a jinych sukkulentu. Brno, 5: 73. as Gymnocalycium valnicekianum.
Massimo Meregalli & Graham J. Charles (2008) Cactaceae Systematics Initiatives: Bulletin of the International Cactaceae Systematics Group, 24: 25.  as Gymnocalycium mostii subsp. valnicekianum

 

Gymnocalyciums: Gymnocalycium valnicekianum

Gymnocalycium valnicekianum

 

Mescaline reported in small amounts.

Origin: Argentina (Córdoba & El Zapata). (500-)900-1300(-1500)m.

Habitat: Grows among tall grasses in mossy cracks and cavities in rocky cliffs. Cactus-Art.

Broadly spherical at first, later growing spherical to elongated; up to 30 cm high and 18 cm in diameter, sometimes offsetting. Pilbeam notes it to grow larger in cultivation.
Epidermis is smooth and dark grass-green.
Around 10(-13) ribs with swollen, rounded, chin-like tubercles and elliptical areoles with light grey wool.
Spine are variable in number, 7-15 or more. They are whitish-grey to
dirty white, and thickened below. 1-6 central spines. Spines have darker tips at first.”The plants in habitat are each one different from its neighbours! Some had strong spines others weak, curly, straight, long or short ones and in all different combinations” Cactus-Art

Flowers are white with a reddish throat and reddish striped outer petals; 5 cm dia.
Seeds are matt black.
Backeberg 1977 page 195
Pilbeam 1995: 151-152 (Fig. 97)

 Koehres offers var. polycentrale

Schütz also distinguishes var. centrispinum.

 

IUCN lists Gymnocalycium mostii as a species of “Least Concern” due to there being abundance of plants, no significant threats and occurrence in a protected range.
Demaio, P. & Trevisson, M. 2013. Gymnocalycium mostii. The IUCN Red List of Threatened Species. Version 2014.2. <www.iucnredlist.org>. 

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

 

 

Gymnocalycium vatteri  Buining

Albert Frederik Hendrik Buining (1950) Succulenta, 66 (1950), as Gymnocalycium vatteri.
Wolfgang Papsch (1993) Gymnocalycium, 6 (1): 79, as Gymnocalycium ochoterenae subsp. vatteri, spelling as ‘ochoterenai‘.
Pilbeam 1995 dismissed the merger by Papsch and a new proposed variety of vatteri, also by Papsch, on the basis of the species known high degree of variability.

 

Gymnocalyciums: Gymnocalycium vatteri

Gymnocalycium vatteri

Mescaline has been reported in small amounts.

Origin: Argentina (Córdoba, Sierra Grande, near Nono). 800-1000m.

Habitat: Amidst rocks and grasses.

Buining 1950 Succulenta, 66, Latin diagnosis of G. vatteri

Buining 1950 Succulenta, 66, Latin diagnosis of G. vatteri

 

Solitary typically but offesetting around the base with age.
Starting flattened hemisperical at first, growing to 4 cm high and 9 cm in diameter.

Epidermis is matt, olive green.
(8-)11(-16), ribs; up to 2.5 cm across and uo to 12 mm high.
Tubercles are swollen and humped, possessing an acute transverse notch beneath.
Areoles are somewhat depressed, ~5 mm wide with grey wool.
3(-5) [1 or 2, sometimes 3 in Pilbeam) Radial spines are appressed or projecting; Pilbeam notes them standing out in youth but curving towards the body with age. They are up to 2 cm and thicker at their base; horn-colored or a dirty darker color.
Spines on the lower part of the plant are variable in both length and curvature but are fairly stout and also sometimes projecting; other spines may be bent and closely appressed.
White flower with a reddish throat in Backeberg and a brownish-grey throat in Pilbeam. 5 cm. long and 4 cm in diameter.
Glossy, light brown seeds; 1 mm in length.
There is a form with more conspicuously claw-like spines but they can also be irregularly interlacing.
Backeberg 1977: page 195 (Fig. 146)
Pilbeam 1995: 152-153 (Fig. 98)

 

Hardy to -5°C. Light shading is recommended. Cactus-Art. Pilbeam describes as slow growing.

 

Gymnocalyciums: Gymnocalycium vatteri

Gymnocalycium vatteri

 

Koehres offers var. cereiformis

 

Gymnocalyciums: Gymnocalycium vatteri

Gymnocalycium vatteri

 

 

External resources:

Cactus-Art

Gymnocalycium.free.fr

 

 

 All of Dr. Štarha’s values for the next section were determined by GC and/or GC-MS. All of the plants that he analyzed were grown from seed in Czechoslovakian greenhouses.

 

Reports of mescaline within the Gymnocalycium species

Synonyms are often mentioned but expect them to keep changing as long as humans keep trying to categorize plants.

Gymnocalyciums: Gymnocalycium achirasense flower

Gymnocalycium achirasense

Gymnocalycium achirasense Till & Schatzl

 Tyramine (0.00159% [± 0.00008])

 N-Methyltyramine (0.00045% [± 0.00006])

 Hordenine (0.00129% [± 0.00006])

 Mescaline (0.00007% [± 0.00001])

 N-Methylmescaline (0.00013% [± 0.00001])

 N,N-Dimethylmescaline (0.00025% [± 0.00002])

 Anhalamine (0.00097% [± 0.00001])

     Štarha et al. 1998 (% by fresh weight)

 [All of Starha’s values in this genus are expressed as % by fresh weight.]

 
Gymnocalyciums: Gymnocalycium-monvillei-Paraguay-6848-EWerdermann-sn-HBG-2006

Gymnocalycium monvillei

 

Gymnocalyciums: Gymnocalycium-asterium-v-paucispinum

Gymnocalycium asterium var. paucispinum

Gymnocalycium asterium Ito

(now merged with Gymnocalycium stellatum)

 Tyramine (0.00089% [± 0.00013])

 N-Methyltyramine (0.00012% [± 0.00004])

 Hordenine (0.00105% [± 0.0001])

 Mescaline (0.00013% [± 0.00002])

 N-Methylmescaline (0.00031% [± 0.00004])

 N,N-Dimethylmescaline (0.0005% [± 0.00004])

 O-Methylanhalidine (0.00011% [± 0.00002])

 Anhalidine (Trace)

 Anhalamine (0.00054% [± 0.00002])

 Anhalonidine (Trace)

 Pellotine (Trace)

 Anhalonine (Trace)

 Lophophorine (Trace)

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium-asterium

Gymnocalycium asterium

Compare the analysis of G. asterium to that of G. stellatum.

Gymnocalyciums: Gymnocalycium-baldianum-flowera

Gymnocalycium baldianum

Gymnocalycium baldianum (Spegazzini) Spegazzini

  Tyramine (less than 0.0001%)

  Hordenine (approximately 0.001%)

  Mescaline (less than 0.0001%)

  Anhalinine (less than 0.0001%)

  Anhalidine (less than 0.0001%)

  Anhalamine (less than 0.0001%)

  Anhalonidine (less than 0.0001%)

  Pellotine (less than 0.0001%)

  Anhalonine (less than 0.0001%)

  Lophophorine (less than 0.0001%)

      Štarha 1996

 Reported to contain Betalains as pigments. Wohlpart & Mabry 1968
cited Dreiding 1961

 

Gymnocalyciums: Gymnocalycium calochlorum

Gymnocalycium calochlorum

Gymnocalycium calochlorum (Boedecker) Y.Itô

  Mescaline (between 0.0001-0.001%)

 Tyramine (between 0.0001-0.001%)

  N-Methyltyramine (less than 0.0001%)

  Hordenine (approximately 0.001%)

  N-Methylmescaline (less than 0.0001%)

  Anhalinine (less than 0.0001%)

  Anhalidine (less than 0.0001%)

  Anhalamine (less than 0.0001%)

  Anhalonidine (between 0.0001-0.001%)

  Pellotine (less than 0.0001%)

      Štarha 1996 (% by fresh weight)

Gymnocalyciums: Gymnocalycium calochlorum

Gymnocalycium calochlorum

Gymnocalycium carminanthum Borth & Koop

 Tyramine (0.00007% [± 0.00003])

 N-Methyltyramine (Trace)

 Hordenine (0.00016% [± 0.00005])

 Mescaline (0.00006% [± 0.00005])

 N-Methylmescaline (Trace)

 N,N-Dimethylmescaline (0.00008% [± 0.00002])

 O-Methylanhalidine (0.00007% [± 0.00002])

 Anhalamine (0.00088% [± 0.00003])

 Anhalonidine (Trace)

     Štarha et al. 1998 (% by fresh weight)

 

Gymnocalycium comarapense Backeberg

 Tyramine (Between 0.001-0.001%)

 N-Methyltyramine (Less than 0.001%)

 Hordenine (Less than 0.001%)

 Mescaline (Less than 0.001%)

 N-Methylmescaline (Less than 0.001%)

 Anhalamine (Less than 0.001%)

 Pellotine (Less than 0.001%)

     Štarha 1995 (% by fresh weight)

Gymnocalyciums: Gymnocalycium-denudatum-HBG

Gymnocalycium denudatum

Gymnocalycium denudatum (Link & Otto) Pfeiffer

 Tyramine (0.00066% [± 0.00006])

 N-Methyltyramine (0.00061% [± 0.00002])

 Hordenine (0.00052% [± 0.00005])

 Mescaline (Trace)

 N-Methylmescaline (0.00008% [± 0.00001])

 N,N-Dimethylmescaline (0.00073% [± 0.00005])

 O-Methylanhalidine (0.00025% [± 0.00003])

 Anhalinine (0.00006% [± 0.00002])

 O-Methylanhalonidine (0.0001% [± 0.00002])

 Anhalidine (Trace)

 Anhalamine (0.00048% [± 0.00002])

 Anhalonidine (Trace)

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium fleisheranum

Gymnocalycium fleisheranum

Gymnocalycium fleischerianum Backeberg

(Now considered

  Tyramine (0.0001-0.001% dry wt.)

  N-Methyltyramine (0.001% dry wt.)

  Hordenine (0.0001-0.001% dry wt.)

  Mescaline (0.0001-0.001% dry wt.)

  N-Methylmescaline (0.0001-0.001% dry wt.)

  N,N-Dimethylmescaline (0.0001-0.001% dry wt.)

  Anhalamine (0.0001-0.001% dry wt.)

  Anhalonidine (0.00001-0.0001% dry wt.)

    Štarha 2001c did not include a citation for this information. (G. fleischerianum is included only in his table on page 91 and not in the by species breakdown)

Gymnocalyciums: Gymnocalycium fleisheranum

Gymnocalycium fleisheranum

 

Gymnocalyciums: Gymnocalycium gibbosum

Gymnocalycium gibbosum

Gymnocalycium gibbosum (Haworth) Pfeiffer

 92.1% water by weight (pH of juice: 4.6-5.0) Herrero-Ducloux 1930b

  Tyramine (Less than 0.0001%) Štarha et al. 1997

  N-Methyltyramine (approximately 0.001%) Štarha et al. 1997

  Hordenine (approximately 0.001%) Štarha et al. 1997

  Mescaline (unquantified and tentatively identified. Colorless birefringent crystals, n 1.544, mp 160-162o were claimed to show the “reactions of mescaline”) Herrero-Ducloux 1930b. Mescaline was NOT observed by Štarha
et al. 1997.

 N-Methylmescaline (Between 0.0001-0.001%) Štarha et al. 1997

  N,N-Dimethylmescaline (Less than 0.0001%) Štarha et al. 1997

  O-Methylanhalidine (approximately 0.001%) Štarha et al. 1997

  Anhalinine (approximately 0.001%) Štarha et al. 1997

  O-Methylanhalonidine (approximately 0.001%) Štarha et al. 1997

  Anhalidine (Between 0.0001-0.001%) Štarha et al. 1997

  Anhalamine No quantification (or accurate identification) attempted; Herrero-Ducloux 1930b [Our source was Reti; CA gives this as Anhalonine. I presently lack the primary paper.] (approximately 0.001%) Štarha et al. 1997

  Anhalonidine (Less than 0.0001%) Štarha et al. 1997

  Pellotine (Between 0.0001-0.001%) Štarha et al. 1997

  Anhalonine (Between 0.0001-0.001%) Štarha et al. 1997

  Lophophorine No quantification (or accurate identification) attempted; Herrero-Ducloux 1930b. Between 0.0001-0.001%: Štarha et al. 1997

 Gymnocalycium horridispinum Frank

  Mescaline (between 0.0001-0.001%)

  Tyramine (approximately 0.001%)

  N-Methyltyramine (less than 0.0001%)

  Hordenine (approximately 0.001%)

  N-Methylmescaline (less than 0.0001%)

  Anhalinine (less than 0.0001%)

  Pellotine (less than 0.0001%)

      Štarha 1996 (% by fresh weight)

Gymnocalyciums: Gymnocalycium leeanum

Gymnocalycium leeanum

Gymnocalycium leeanum (Hooker) Br. & R.

[Now considered

  Anhalonine (Unconfirmed) Herrero-Ducloux 1930b

 Not observed by DeVries et al. 1971

  Hordenine (%?) DeVries et al. 1971

  Lophophorine (Unconfirmed) Herrero-Ducloux 1930b

 Not observed by DeVries et al. 1971

  Mescaline (Unconfirmed) Herrero-Ducloux 1930b

 Not observed by DeVries et al. 1971

  N-Methyltyramine  (?%) DeVries et al. 1971

  Tyramine (0.00583%) DeVries et al. 1971

Gymnocalyciums: Gymnocalycium leeanum

Gymnocalycium leeanum

 

 

Gymnocalyciums: Gymnocalycium-mesopotamicum-HBG

Gymnocalycium mesopotamicum

 Gymnocalycium mesopotamicum Kiessling

 Tyramine (Trace)

 N-Methyltyramine (Trace)

 Hordenine (Trace)

 Mescaline (Trace)

 N-Methylmescaline (Trace)

 N,N-Dimethylmescaline (0.00279% [± 0.0005])

 Anhalamine (0.0019% [± 0.00028])

 Anhalonidine (0.00005% [± 0.00003])

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium-monvillei-Paraguay-6848-EWerdermann-sn-HBG-2006

Gymnocalycium monvillei

 Gymnocalycium monvillei (Lemaire) Britton & Rose

 Tyramine (Between 0.0001-0.001%)

 N-Methyltyramine (Between 0.0001-0.001%)

 Hordenine (Approximately 0.001%)

 Mescaline (Less than 0.0001%)

 N-Methylmescaline (Less than 0.0001%)

 N,N-Dimethylmescaline (Less than 0.0001%)

 O-Methylanhalidine (Less than 0.0001%)

 Anhalinine (Less than 0.0001%)

 O-Methylanhalonidine (Less than 0.0001%)

 Anhalidine (Less than 0.0001%)

 Anhalamine (Less than 0.0001%)

 Anhalonidine (Between 0.0001-0.001%)

 Pellotine (Between 0.0001-0.001%)

 Anhalonine (Between 0.0001-0.001%)

 Lophophorine (Less than 0.0001%)

     Štarha et al. 1997 (% by fresh weight)

 

Gymnocalycium moserianum Schutz

 Tyramine (0.00077% [± 0.0001])

 N-Methyltyramine (0.0001% [± 0.00003])

 Hordenine (0.00011% [± 0.00003])

 Mescaline (0.00007% [± 0.00001])

 N-Methylmescaline (0.00151% [± 0.00015])

 N,N-Dimethylmescaline (0.00071% [± 0.00006])

 O-Methylanhalidine (0.00007% [± 0.00001])

 Anhalinine (0.00007% [± 0.00001])

 O-Methylanhalonidine (0.00007% [± 0.00001])

 Anhalidine (0.00007% [± 0.00001])

 Anhalamine (0.00215% [± 0.00014])

 Anhalonidine (0.00014% [± 0.00003])

 Pellotine (0.00012% [± 0.00003])

 Anhalonine (Trace)

 Lophophorine (Trace)

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium multiflorum

Gymnocalycium multiflorum

Gymnocalycium multiflorum

(Now considered to be at least partially a synonym with Gymnocalycium monvillei.)

Herrero-Ducloux 1932a reported recovering small quantities of a ‘mescaline-like’ alkaloid from this species.

This report for this cactus species presently lacks confirmation.

 

 Gymnocalycium netrelianum Britton & Rose

 Tyramine (Less than 0.001%)

 Hordenine (Between 0.0001-0.001%)

 Mescaline (Between 0.0001-0.001%)

 N-Methylmescaline (Less than 0.001%)

 Pellotine (Less than 0.001%)

     Štarha 1995a (% by fresh weight)

Gymnocalycium nigriareolatum Backeberg

 Tyramine (0.00047% [± 0.00005])

 N-Methyltyramine (0.00008% [± 0.00002])

 Hordenine (0.0014% [± 0.00006])

 Mescaline (0.00006% [± 0.00002])

 N-Methylmescaline (0.00006% [± 0.00001])

 N,N-Dimethylmescaline (0.00009% [± 0.00002])

 O-Methylanhalidine (0.00012% [± 0.00006])

 Anhalamine (0.00019% [± 0.00004])

 Anhalonidine (0.00008% [± 0.00002])

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium-oenanthemum

Gymnocalycium oenanthemum

Gymnocalycium oenanthemum Backeberg

 Tyramine (Between 0.0001-0.001%)

 N-Methyltyramine (Less than 0.0001%)

 Hordenine (approximately 0.001%)

 Mescaline (Less than 0.0001%)

 N-Methylmescaline (Less than 0.0001%)

 N,N-Dimethylmescaline (Less than 0.0001%)

 O-Methylanhalidine (Less than 0.0001%)

 O-Methylanhalonidine (Less than 0.0001%)

 Anhalidine (Less than 0.0001%)

 Anhalamine (Less than 0.0001%)

 Anhalonidine (Between 0.0001-0.001%)

 Pellotine (Between 0.0001-0.001%)

 Anhalonine (Less than 0.0001%)

 Lophophorine (Less than 0.0001%)

      Štarha et al. 1997 (% by fresh weight)

Gymnocalycium paraguayense Schutz

 Tyramine (0.00047% [± 0.00004])

 N-Methyltyramine (0.00104% [± 0.00014])

 Hordenine (0.00043% [± 0.00008])

 Mescaline (0.00011% [± 0.00006])

 N-Methylmescaline (0.00041% [± 0.0001])

 N,N-Dimethylmescaline (0.00427% [± 0.00032])

 Anhalamine (0.00505% [± 0.0005])

 Anhalonidine (0.00017% [± 0.00006])

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium-quehlianum

Gymnocalycium quehlianum

Gymnocalycium quehlianum (Haage) Berg.

  Tyramine (Between 0.0001-0.001%)

  N-Methyltyramine (Between 0.0001-0.001%)

  Hordenine (approximately 0.001%)

  Mescaline (Less than 0.0001%)

  N-Methylmescaline (Less than 0.0001%)

  N,N-Dimethylmescaline (Less than 0.0001%)

  Anhalinine (Less than 0.0001%)

  O-Methylanhalonidine (Between 0.0001-0.001%)

  Anhalonidine (Less than 0.0001%)

  Pellotine (Less than 0.0001%)

  Anhalonine (Less than 0.0001%)

  Lophophorine (Less than 0.0001%)

      Štarha et al. 1997 (% by fresh weight)

 Gymnocalycium ragonesii Cast.

 Tyramine (0.00009% [± 0.00002])

 N-Methyltyramine (0.00005% [± 0.00001])

 Hordenine (0.0035% [± 0.00014])

 Mescaline (Trace)

 N-Methylmescaline (Trace)

 N,N-Dimethylmescaline (Trace)

 O-Methylanhalidine (0.00048% [± 0.00003])

 Anhalinine (0.00109% [± 0.00018])

 O-Methylanhalonidine (0.00007% [± 0.00001])

 Anhalidine (0.00006% [± 0.00001])

 Anhalonidine (Trace)

 Pellotine (Trace)

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium riograndense

Gymnocalycium riograndense Cardeñas

(Now Gymnocalycium pflanzii subsp. zegarrae)

Tyramine (Between 0.0001-0.001%)

 N-Methyltyramine (Less than 0.001%)

 Hordenine (Less than 0.001%)

 Mescaline (Between 0.0001-0.001%)

 N-Methylmescaline (Less than 0.001%)

 Anhalinine (Less than 0.001%)

 Anhalidine (Less than 0.001%)

 Anhalonidine (Less than 0.001%)

 Pellotine (Less than 0.001%)

 Anhalonine (Less than 0.001%)

 Lophophorine (Less than 0.001%)

     Štarha 1995a (% by fresh weight)

Gymnocalycium riojense Fric ex H.Till & W.Till

  Tyramine (0.001% dry wt.)

  N-Methyltyramine (0.00001-0.0001% dry wt.)

  Hordenine (0.001% dry wt.)

  Mescaline (0.00001-0.0001% dry wt.)

  N-Methylmescaline (0.00001-0.0001% dry wt.)

  Anhalinine (0.00001-0.0001% dry wt.)

  O-Methylanhalonidine (0.00001-0.0001% dry wt.)

  Pellotine (0.00001-0.0001% dry wt.)

  Anhalonidine (0.00001-0.0001% dry wt.)

     Štarha 2001c cited Štarha 2001a

Gymnocalyciums: Gymnocalycium-stellatum-HBG

Gymnocalycium stellatum

Gymnocalycium stellatum Spegazzini

  Tyramine (Between 0.0001-0.001%)

  N-Methyltyramine (Less than 0.0001%)

  Hordenine (approximately 0.001%)

  Mescaline (Less than 0.0001%)

  N-Methylmescaline (Between 0.0001-0.001%)

  N,N-Dimethylmescaline (Less than 0.0001%)

  Anhalinine (Between 0.0001-0.001%)

  O-Methylanhalonidine (Less than 0.0001%)

  Anhalamine (Less than 0.0001%)

  Anhalonidine (Between 0.0001-0.001%)

  Pellotine (Between 0.0001-0.001%)

  Anhalonine (Between 0.0001-0.001%)

  Lophophorine (Less than 0.0001%)

      Štarha et al. 1997 (% by fresh weight)

Gymnocalycium striglianum Jeggle

  Tyramine (Less than 0.001%)

 Hordenine (Less than 0.001%)

 Mescaline ( “readily apparent” at around 0.001%)

 N-Methylmescaline ( “readily apparent” at around 0.001%)

 Anhalinine (Less than 0.001%)

 Anhalidine (Less than 0.001%)

 Anhalamine ( “readily apparent” at around 0.001%)

 Anhalonidine (Less than 0.001%)

 Pellotine ( “readily apparent” at around 0.001%)

 Anhalonine (Less than 0.001%)

 Lophophorine (Less than 0.001%)

     Štarha 1995a (% by fresh weight)

Gymnocalyciums: Gymnocalycium triacanthum

Gymnocalycium triacanthum

Gymnocalycium triacanthum Backeberg

 Tyramine (Trace)

 N-Methyltyramine (0.00005% [± 0.00001])

 Hordenine (0.00054% [± 0.00004])

 Mescaline (Trace)

 N-Methylmescaline (Trace)

 N,N-Dimethylmescaline (Trace)

 O-Methylanhalidine (0.00015% [± 0.00001])

 Anhalinine (0.00014% [± 0.00001])

 Anhalidine (Trace)

 Anhalonidine (0.0006% [± 0.00001])

     Štarha et al. 1998 (% by fresh weight)

Gymnocalyciums: Gymnocalycium triacanthum

Gymnocalycium triacanthum

Gymnocalycium uebelmannianum Rausch

  Tyramine (Between 0.0001-0.001%)

  N-Methyltyramine (Between 0.0001-0.001%)

  Hordenine (Between 0.0001-0.001%)

  Mescaline (Between 0.0001-0.001%)

  N-Methylmescaline (Less than 0.0001%)

  N,N-Dimethylmescaline (Less than 0.0001%)

  O-Methylanhalidine (Less than 0.0001%)

  Anhalinine (Between 0.0001-0.001%)

  O-Methylanhalonidine (Between 0.0001-0.001%)

  Anhalidine (Less than 0.0001%)

  Anhalamine (Between 0.0001-0.001%)

  Anhalonidine (Between 0.0001-0.001%)

  Pellotine (Between 0.0001-0.001%)

  Anhalonine (Less than 0.0001%)

  Lophophorine (Less than 0.0001%)

      Štarha et al. 1997 (% by fresh weight)

Gymnocalyciums: Gymnocalycium valnicekianum

Gymnocalycium valnicekianum seedling

Gymnocalycium valnicekianum Jajó

(now Gymnocalycium mostii subsp. valnicekianum)

 Tyramine (Between 0.0001-0.001%)

 N-Methyltyramine (Less than 0.001%)

 Hordenine ( “readily apparent” at around 0.001%)

 Mescaline (Less than 0.001%)

 Anhalinine (Less than 0.001%)

 Anhalonidine (Between 0.0001-0.001%)

 Pellotine (Less than 0.001%)

 Anhalonine (Less than 0.001%)

 Lophophorine (Less than 0.001%)

     Štarha 1995a (% by fresh weight)

Gymnocalyciums: Gymnocalycium vatteri

Gymnocalycium vatteri

 Gymnocalycium vatteri Buining

(now Gymnocalycium ochoterenae subsp. vatteri, or not; depending upon with whom you want to agree.)

  Mescaline (between 0.0001-0.001%)

  Tyramine (approximately 0.001%)

  N-Methyltyramine (between 0.0001-0.001%)

  Hordenine (approximately 0.001%)

  N-Methylmescaline (between 0.0001-0.001%)

  Anhalinine (approximately 0.001%)

  Anhalidine (less than 0.0001%)

  Anhalonidine (between 0.0001-0.001%)

  Pellotine (between 0.0001-0.001%)

  Anhalonine (less than 0.0001%)

  Lophophorine (less than 0.0001%)

      Štarha 1996 (% by fresh weight)

Gymnocalyciums: Gymnocalycium vatteri

Gymnocalycium vatteri

 

 

 Parting comment on the genus Gymnocalycium and South American globulars:

 It is puzzling that this large genus and area has been neglected for so many years, in light of the intense academic interest which has intermittently surrounding such plants.The work of Dr. Štarha underscores the need for more in depth work. While the reported concentrations overall are low, this is in line with the majority of cacti tested; the high mescaline producers are only sporadically represented and apparently difficult to predict.  Štarha’s results are encouraging despite low values.

 Considering how many different Gymnocalycium species are readily available, how easy they are to grow, how often this is mentioned in the literature and how many of the larger flat species actually resemble Peyote in color and appearance, it is mind boggling that more people have not pursued further chemical work in this fascinating and attractive group.

 G. platense and G. riograndensis have long been suggested as probable mescaline containing species but, as far as it can be determined, this was implied solely by morphology as no actual chemical work had been done. More recently, Dr. Štarha did indeed find small amounts of mescaline in the latter.

 An interesting mention is made of globular cacti in Margaret Ashley Towle 1961. Her reference, Eugenio Yácovleff & Fortunato L. Herrera 1934, mention Lobivia (L. corbula), Mammillaria (M. herrerae) (equating these first two) and Melocacti in passing, during their discussion of the many varied forms of cacti found depicted in ceramic designs. (pages 319-320, ceramic design examples also on page 321). [Their reference to Melocacti was in regards to the Peruvian species which form distinct Cereus-like columns somewhat resembling Neoraimondia and Armatocereus species but it should be mentioned that most Melocacti exist as fairly globular plants.]

 Some types of globular cacti are clearly depicted. While mescaline has not yet been reported from these plants, many Lobivia, Mammillaria, Melocacti, and Echinopsis species, as well as additional non-mescaline containing Gymnocalyciums, have all been reported to contain alkaloids.

 I would suggest more representative species be examined for all.

Azketium ritteri

Aztekium ritteri (Bödeker) Bödeker

Friedrich Boedeker  (1929) Monatsschrift für Kakteenkunde, 1: 52. Aztekium ritteri
Friedrich Boedeker  (1928) Zeitschrift für Sukkulentenkunde. Berlin 3 (14): 305–306. Echinocactus ritterii


Aztekium ritteri

 

Small amounts of mescaline have been reported. 

Etymology: The wonderful texture of its surface has been likened to some Aztec motifs, hence the genus name Aztekium. Friedrich Ritter (who had been living in Mexico) was the specific namesake.

Habitat: From Nuevo Leon, Mexico growing in xeric scrub on limestone and gypsum cliffs.

Often remains solitary but may be freely offsetting from base with age (or if grafted or after exposure to pesticides & fungicides). 
Greyish-green to grey body is broad and rounded to around 2 inches in
diameter; with a depressed wooly top.

Short napiform taproot.
9-11 ribs, [Ed.: Sometimes swirling] folded, with subsidiary and narrower ribs in between.] 
Cultivated plants tend to be more green. Especially so on grafted plants. This is considered a detractant to the beauty of this plant by most authorities and serious collectors.
Areoles are closely set and bear white hairs.
Few spines; weak, bent or contorted. Usually 1-3; 3-4 mm in length.
White flowers 8 mm in diameter, appearing to have a stalk.
[Pizetti describes flowers as being about 1 cm wide; with white segments and outer perianth parts with pink edges. Anderson 1998 describes the flowers as white to light pink and appearing sporadically throughout the summer.]
Pink fruit is berrylike and appears only when ripe.
Black seeds are 0.5 mm long.
    Backeberg 1977: 79-80 and
    Pizetti 1985 entry #15.

Backeberg noted that there is also a form with flower that is longer (has longer stalk)

See also Backeberg 1961 [5: 2890-2892], (includes pictures on page 2891, fig. 2722, and the larger flowered form in flower, fig. 2723.) and Lamb & Lamb 1971 [2: 378] (with picture). Pizetti has color picture.

Habitat photos: Chastek 1994 Kaktusy 2: 40-41

Backeberg & Pizetti (& many others) describe the species as cold sensitive but I have seen them tolerate hard freezes (6°F) in a covered but unheated outdoor cactus bed Austin Texas when totally dry. I would recommend protection from freezing despite that lucky experience.

Once considered an endangered species due to being found only in a restricted area experiencing heavy collection activity. More populations across a broad range have since been discovered. The habitat includes inaccessible populations due to restricted access for both humans and browsers so it has been downgraded to become listed as a species of “Least Concern“.
      B. Fitz Maurice & W.A. Fitz Maurice 2013. Aztekium ritteri. The IUCN Red List of Threatened Species. Version 2014.2. www.iucnredlist.org.

Reported analysis:
(Plants greenhouse grown in Czechoslovakia)
N-Methyltyramine (0.0031% by fresh wt.)
3-Methoxytyramine (Less than 0.0001% by fresh wt.)
Hordenine (Less than 0.0001% by fresh wt.)
N,N-Dimethyl-3,4-dimethoxyphenethylamine (0.0036% fresh wt.)
Mescaline (0.0009% by fresh wt.) (Which is not quite a mg per kg.)
Anhalidine (0.0008% by fresh wt.)
Pellotine (0.0026% by fresh wt.)
    Štarha 1994

[Aztekium ritteri has had an unconfirmed claim of caffeine. No reference was cited and none has been located. Claims for caffeine have never been sustantiated in any cactus species.]

Glucaric acid (tlc by Kringstad & Nordal 1975)
Quinic acid (tlc, glc & gc-ms by Kringstad & Nordal 1975)

 

 

Alwin Berger 1929 Kakteen, pp. 259-260.

Aztekium ritteri description

 

External links:

Dave’s Garden’s

IPNI

ThePlantList

Tropicos

the Peyote Crisis and some Suggestions – Revisited

This article and the rest of the book Sacred Cacti are now best viewed at http://sacredcacti.com  My apologies for any 404 pages resulting from any link on this website that is being overlooked by me.
It appears to be a ripe time for reevaluating the article entitled “the Peyote crisis & some suggestions“.
This was variously positioned as Chapter 2 or Chapter 3 in the revisions of the book Sacred Cacti.
That chapter, as written, is greatly in need of revision & updating; and some additional questions being asked about *its* suggestions. Our use of the word “I” in this article simply means we want to say this with one voice. Use of the word “we” refers to the reader and ourselves.
This commentary, as written, is meant to serve the great need for better accurate public education and has been constructed primarily for clarity of presentation of the contained material. It has not been created with the same density of in-line references such as would be the case for a work that was intended for print publication in a peer reviewed journal. It is hoped that adequate documentation and references are included for the benefit of people wanting to learn more but if YOU want to learn more or need any additional clarification or supportive documentation please drop an email to keepertrout at gmail and ask.
Accompanying this information is the feeling that there is some urgency in it being released. It is therefore being made available for public inspection and comment without further delay.
The plants of tomorrow begin with the seeds that are planted today.

Commentary & thoughts
by Keeper Trout, Blake Edwards & Martin Terry

I also went to survey the gardens in February [1998]. The situation is sad, intolerable, several parcels hunted completely clean. On inquiring with the dealers, I was able to hand sort well over 10,000 dime sizers, most w/roots. They are picked that way because the payment is per unit. […] those 10,000 plus babies are now growing. My idea is to purchase all the babies we can for their eventual re-planting in Texas.”
Leo Mercado 6 July 1998 (personal communication).

Those same plants were later seized (as part of a dump-truck load containing more than 11,230 living peyote plants) and destroyed by a “multijurisdictional task-force” of law enforcement officials despite Leo at that time having been found in court to be in compliance with Arizona state law permitting the sincere religious use of peyote. In the aftermath of what can only legitimately be described as a terroristic home invasion, Leo posted a notice online that he had replanted the 200 or so peyote plants that had been missed or dropped during the raid.
No charges were filed, which fact was likely to prevent a return of his peyote as had occurred after the first time that they seized Leo’s peyote. Instead Leo’s landlord found himself being threatened with the seizure and forfeiture of his property if he did not evict Leo and his family. The basis of that threat was his supposedly renting to a “known illegal drug dealer”, namely Leo!
Apparently Leo’s living example as a human of only modest means successfully propagating and cultivating large numbers of peyote plants outside of Texas was too powerful of an example to be allowed to exist. At the very least, his Kearny, Arizona shade-house and gardens had to be seen as an awkward truth running counter to the lies actively being propagated about it being impossible to grow peyote outside of its native habitat.
From Ch. 3 in Sacred Cacti 3rd edition (with some edits).

 

Lophophora-williamsii-threatened-by-knife

Cutting crowns flush at the level of the ground has been established to be the best known harvesting technique for peyote. This approach to enable sustainable harvesting has been known of and employed by peyote consumers in Mexico for millenia. The archaeological peyote specimens discovered strung on a cord at Cuatro Cienegas are more than a thousand years old; the Shumla peyote effigies are over six thousand years old.

 

First, concerning the “crisis”….

One suggestion, really, is all that is required; assuming that it can be heard, without prejudice, where it matters.

Cultivate the Medicine.

It is really simple yet that simple truth of the matter has been almost completely buried, if not forgotten or deliberately obscured, in rhetoric that has at times variously been self-serving, manipulative, deceptive, disingenuous, confused, based on misunderstandings, culturally bigoted, or sometimes even entirely delusional. There really was not any delicate way to put that so I apologize for trodding on anyone’s conceptual toes.

Some people might ask:
If peyote is a pressured species, why isn’t it cultivated?

The question, “why isn’t it cultivated?” is a really good one. You and I will be exploring its answers in some detail.

We should start by clarifying some things and being certain that we all have a good grasp of an unnecessarily convoluted story.

 

The conservation status of peyote

Peyote is most certainly not extinct as some people strangely seem to believe and are even willing to say openly as if it were a fact. It is not yet really even an endangered species as more than a million living peyote crowns were no doubt harvested in South Texas again this past year by the licensed peyote distributors (I have to say probably as the numbers are not yet available).

A perception that the pressure from peyote harvesting is endangering the species is nothing new. While it does not appear on any federal listing of endangered species, peyote WAS declared an endangered species by the Texas Organization of Endangered Species (TOES) according to Morgan 1983: 83-84. Despite having a long history of cost sharing with land owners for brush removal and clearing of land, since the late 1970’s the U.S. Soil Conservation Service has refused to do so in any area containing peyote, as the SCS recognizes it to be a potentially endangered member of Texas flora (Morgan 1984: 292). Their lack of financial contribution has not slowed the clearing of land in the development of South Texas.

Only recently was peyote actually finally recognized as having adequately dwindling numbers to merit being assigned a status of “vulnerable” and being placed on the IUCN Red List of Threatened Species. Version 2013.2. [http://www.iucnredlist.org/details/151962/0].

Debates as to whether it should or should not be placed on the Red List had been going back and forth for some years, Oddly, what seems to have tipped the balance of opinion was the appearance of cosmetic/pharmaceutical industry products known as Pomada de Peyote. [Link 1] [Link 2] [Link 3] [Link 4] [Link 5].
I’m not including these links to suggest that any should be patronized but simply to note what came up in a Google search for “pomada de peyote” on 1 November, 2014.
Here are images of five of the products that were found to be offered on the first search results page.

 

Pomada-de-Peyote

 

It is certain that as both a liniment and an ointment, similar formulations have existed for a very long time at the folk level, and more recently as products of a local cottage industry. These products have likely achieved visibility only when the distribution venue was moved from local yerbarias to online marketing.

The use of peyote is traditional among some Hispanics in South Texas, too.
“When I was younger, you could buy it at the market in Nuevo Laredo, or at any of the local yerberias (herb shops),” [Salvador] Johnson said.
His wife, Vicenta, said that elderly Hispanics still use the drug as a cure for a variety of ailments, including as a rubbing lotion to treat arthritis when it is mixed with alcohol.
Grant 2000 Ft. Worth Star-Telegram, Sunday, 23 January.

One of the companies now producing pomada de peyote is an established business that is substantial in size and has previously developed other successful product lines. The future development of this product will be interesting to watch. It may be noteworthy that the number of different producers showing up as hits on the first Google search result page went from two to five within the past year.

Peyote is not endangered as a species for a variety of reasons. The most notable being that there are large expanses of the Mexican peyote populations left. The secondary reason is that not all peyote is accessible for harvest. In some cases, harvests are deterred by a lack of road access but in at least one instance a local population (in Mexico) is protected by the resident humans who interestingly do not use their local peyote for any purposes other than as an external analgesic applied to burns, bruises and aching muscles & joints.

In Texas it is a different story. The vast majority of its peyote populations have long since been removed during the course of the modern-day occupation/development of South Texas real estate and the collateral development of its assorted resources. Some peyote finds protection on large ranches with tall fences designed to retain game animals that are hunted for a hefty fee. When the owners of such large tracts of brush also do not permit peyote harvesters to access their land those properties form unintentional peyote reserves. The land that is left as accessible is heavily impacted by the existing peyote trade. In addition, the commercial peyote harvest has been insufficient for meeting NAC needs for some time.

There are two distinct but inseparable subtopics within this main topic of the threats to peyote, whether those threats are due to habitat loss or over-harvesting or any of the other known challenges that peyote faces.

One is the future of peyote as a species and the other is the future of the NAC as a Medicine-based spiritual organization that has both adequate and uninterrupted access to its Medicine.
We will examine both of those subtopics separately as this overview unfolds.

 

What has happened to create dwindling peyote populations?

Reading the popular press or listening to people talk, one would think that overharvesting by Native Americans or “hippies” is the cause. One or the other or both typically gets the most common and most vocal blame. This is true, despite it being absolutely clear that the vast majority of peyote’s obliteration, both in terms of absolute numbers and in total acreage, has actually been the incidental destruction of populations during the process of land conversion. All other factors combined pale by comparison.

There have been many reasons for this; the development of land for various projects, such as construction projects, shipping centers, parking lots and tract communities, or as a result of the brush suppression methods that enable ranchers to use their land for agriculture or ranching. Once a piece of land has been converted, peyote does not return.

 

peyote gardens today

Aerial view of a portion of the Peyote Gardens in Starr County showing extent of the land use and clearing. Photo clipping came from a topographic map from the US Geological Survey (USGS).

Most of peyote’s habitat in South Texas is covered with a tangle of dense thorny brush. To make their land available for agriculture or cattle, it was once a common practice for landowners to root-plow the soil due to the tendency of the thorny brush to come back with an aggressive vigor after being cleared.
Root-plowing severs the roots below the soil surface thereby weakening whatever of the roots can’t be uprooted and suppressing their ability for good regrowth. Or at least suppressing it for longer than might be the case without it. Repeating the process a few times does help but it is noteworthy that what actually becomes most suppressed is the diversity of life while the actual species that were attempted to be eradicated often go on to become the predominate vegetation.

 

rootplowed land

rootplowed land

Land in Maverick County that was root plowed several decades ago. The ranch foreman claimed that peyote was here before that occurred.
Their most likely intended target for eradication was the Acacia rigidula which comprises about a third of the plants seen in the lower image above.

 

Root-plowing has been determined to have lasting adverse impacts when used in dry regions. In arid environments with abundant limestone, in this case it is present as a calcareous gravel, rainwater dissolves the carbonates and other soluble ions but there is insufficient volume of water to carry what is dissolved more than a fairly short distance into the earth, accumulating and eventually creating a bed of ‘caliche’ at the depth of maximum moisture penetration. Due to rainfall being variable in the total amounts delivered per storm, this eventually forms an irregular gradient of alkali concentrations existing between the caliche and the surface ; with the surface obviously being the most life friendly. The layer of decomposing organic materials at or near the surface adds to the ability of the soil to support life.
This natural zoning develops over long periods of time with whatever level of moisture they DO have accessible. As it becomes increasingly basic with increasing depth this also means that that the surface is most amenable to supporting life. Accompanying that is the observation that, as rains moved part of the soluble alkali into the earth, that action helps make the surface more life friendly.
This fragile balance becomes completely undone with the mixing of the top half meter of soil during root plowing.
In this process, the more basic material that has been migrating away from the surface is partially returned to the surface during the mixing process. Recovery is typically slow since the reduction of the alkalinity at the surface level relies on repeated water percolation over time. The resulting increase of surface alkalinity leads to a die-off of small cover plants following seed germination and adds prolonged difficulty in reestablishing the normal flora. In adjacent areas that are used for agriculture due to being more sandy loamy than gravelly, and additionally due to the topography of the land being flatter & less sloping, this creates problems with blowing dust.

As a result root-plowing is now discouraged for those soil types and when it becomes needed specialized implements are used to selectively remove single plants.
The important thing to understand about root-plowing is that unlike the thorny brush that the root-plowing is intended to eradicate, a single thorough root-plowing will generally permanently exterminate all of the existing peyote on that a given piece of land.
If you want to gain a really solid grasp of this technology and a better understanding about why it would impact peyote so adversely, visit http://YouTube.com and search for “root plow” or “rootplowing“. Nothing describes the process better than watching a root-plow in action.

Other brush-clearing methods are not less destructive to peyote but they do impact the soil and ability of the land to recover less than root-plowing. YouTube can provide looks at modern techniques of “brush clearing in South Texas” as well.

 

root plow

 

Root plow Those fins are designed to force the severed roots to the soil surface and into the sun to dry and die.

 

The root plow is a tool for removing vegetation by cutting it below the soil surface […] killing brush and light vegetation by undercutting it […] at depth from 20 to 50 centimeters (8-20 inches). […] The advantage of the root plow is that it cuts the vegetation below the bud ring, killing brush that would normally resprout if cut at ground level.
US Army 1974 Tactical Land Clearing, p. 3-6

 

root plowing

Trunnion-mounted root-plow in action.
Both scanned photos came from a 1974 US Army
training manual entitled “Tactical Land Clearing”.

A new threat to peyote in South Texas are windfarms which choose the highest points in the Bordas Escarpment for their placement. These of course need an access road permitting both construction and maintenance. Those roads potentially carve through some of what few undisturbed peyote populations still remain in South Texas.

 

What do we actually know about the harvesting of peyote?

Surprisingly little study has been done on the impact of harvesting itself. As far as I am aware, only one organization, a nonprofit group named the Cactus Conservation Institute, has taken the time to learn more despite the immense need for this information as regards both the NAC and peyote conservation. It is clear that the peyote plant is a resilient species or it never could have permitted mass harvests to continue for so many years in the face of diminishing habitat. There are many articles that are available concerning the harvesting of the peyote plant and about its habits and habitat.

It IS known that the best way to cut peyote is at ground level. Cutting too deeply increases mortality and weakens those plants which do manage to recover.
The one existing study on the subject was published in Terry & Mauseth 2006. Using a histological evaluation, it was established that only the stem tissue was capable of producing new growth. Root tissue could only grow roots. A visible clear and sharp line of division was noted to exist between the two tissues.

Peyote harvesters often use a shovel with sharpened edge or a machete. Both of those tools can work great for cutting at ground level or they can be mis-employed and produce a deeply angled cut.

 

a cut peyote

Peyote plant after the crown has been removed

 

What do we know about the impact of peyote harvesting on wild populations?

A simple overview:

More complete details concerning the items in this list can be gleaned at the Cactus Conservation Institute website or in Kalam et al. 2013, Klein et al. 2015, Terry et al 2011, 2012, 2013 & 2014.

1) Peyote harvest causes a small increase in mortality.

2) If harvesting is repeated too frequently, this rate of mortality increases.

3) Harvesting also reduces the amount of harvestable biomass of sacrament per plant.

4) The aforementioned observation (3) is initially obscured by the increase in numbers due to the common occurrence of multiple regrowth. However, the sum total biomass of head (crown) tissue per plant, even after 4 years of uninterrupted regrowth, was still significantly smaller than the biomass of the original single head that had been harvested four years before. The study to determine the minimum sustainable recovery period after harvesting is still not complete, but it now clear that the time required for recovery from a single harvesting event is greater than six years.

5) Analysis has also shown that even after four years the regrowth had regained only half the potency of the original crown. It is not yet known how long it takes for the original potency to be re-established in the regrowth buttons.

6) Current and future seed production contributions to the local population are lost along with the harvested plants. The typical fate for peyote seeds following a harvest is into the trash or compost.
During the late 1990s, Leo Mercado was able to successfully recover (and plant) many thousands of seeds from the piles of hairs and tufts that accumulated from the peyote cleaned in preparation for a large ceremony. That event, at an annual NAC meeting at Mirando City, consumed more than a thousand crowns. (Information from a personal communication with Leo in 1998.)

7) The oldest and largest plants have been selected for by their environment as those are the plants which are best suited to survive the peak adverse periods of weather. These are commonly preferentially harvested – precluding any future contribution they might have made to the genetics of the population.
This last point may be subtle but played out over a long time can become significant. Following the removal of these genetically superior products of natural selection, future adverse periods of weather will likely begin to produce an increased adverse impact on the remaining population.

 

multiple regrowth

Peyote plant with multiple regrowth

 

Recovery

Let’s go over through that overview again but this time from a slightly different angle of thought and consider those factors in terms of recovery.
Recovery after harvesting is a core concept for this subject as it interweaves an impact assessment with a determination of sustainability. If the harvesting of a natural renewable resource is not sustainable, both harvesting and availability are temporary and transient phenomena with an inevitable end point involving either the loss or increased scarcity of that resource. /span>
There is nothing mysterious or unclear about what is being witnessed. A dramatic multiplication of undersized individuals is in fact the classical model resulting from harvesting activities involving an overexploited natural resource, be it fish or ginseng roots. (See Terry & Trout 2013. This link is a PDF file.)

Recovery is best understood not by looking at recovery of the individuals which are involved but of the health of local populations which are composed of many individuals.
Recovery of a population will accordingly have several factors based on what we looked at in our overview:

1) Replacement of the plants which die as a result of harvesting. (Replacement in this case is being considered only in terms of the natural recruitment of new seedlings although cultivation and wildcrafting would also enter the picture in this area. Wildcrafting is the conscious planting of seeds or return of plants in such locations where the plant formerly occurred naturally or could have occurred naturally.) This decrease in survival is thankfully a fairly low rate but it is not insignificant if a field is revisited as each subsequent visit may result in the reharvesting of plants which are still drawing their sustenance from the original reserves of the remaining taproot fragment from their mother and have not yet had time to manage to grow a replacement taproot.
The rate of mortality has increased with each time that reharvesting occurred in what limited study of the topic has occurred so mindfulness is needed not just of how deeply a plant is cut but also when it was last cut. Until after the point that a plant can regrow a taproot it is vulnerable to outright death from loss of its photosynthetic tissues as occurs in harvesting. This subtle but simple fact is somehow often either missed or trivialized: when the crown tissue has been removed the peyote plant loses its ability to use the sunlight. This remains true until after a new crown can be made and it reaches the surface of the ground where it can absorb sunlight to once again photosynthesize and feed itself. Repeated cutting too frequently forces the plant to exhaust its limited reserves and interferes with good regrowth and survival.
Plants that have been harvested need adequate time to replace their missing storage tissues (by photosynthesis in the crowns of the regrowth pups) before being reharvested or their death rate increases; eventually requiring their actual replacement.

2) Regrowing new crown tissue to replace the harvested crown with its equivalent prior to reharvesting.
Even though multiple crowns commonly result following harvesting, it takes some point greater than six years for their combined total weight to match that of the original crown. (The study to determine how long it takes for the sum of the regrowth buttons to equal the weight of the original harvested crown is still ongoing.)
Harvesting prior to following that point of recovery will provide smaller and steadily decreasing volumes of harvests. This is a practice which feeds into the spiral towards smaller, weaker plants with higher loss rates.

3) Recovering the original level of alkaloids.
After four years the average alkaloid level of new growth was only half that of the original crown. It is presently unknown how long it takes for the preharvest alkaloid level to be restored. Harvesting prior to following that point of potency recovery will provide an inferior quality of harvests, requiring consumers to ingest more plants, which also feeds into the extinction vortex towards smaller, weaker plants with higher loss rates.

4) The population also has to recover from the impact of however many years it would take seeds from those harvested plants to be replaced by new seed-producing crowns, and this must be taken into account if wanting to accurately assess the impact of harvesting. Every plant which is taken means that many less seeds are available for the local population for at least a handful of years. This is not insignificant as wild peyote in nature primarily reproduces via seeds. Removing a plant means removing all future seed contribution by that plant.
If older plants are preferentially harvested and as numbers dwindle the age of first harvest also decreases, it rapidly produces a situation where the only plants to harvest may have flowered only once or twice or not at all, creating a huge seed production deficit for the local population.
In the event of adverse weather (whether prolonged drought or beyond average freezing) causing an above average loss rate, this adds to the risk that the local population may not recover.

I’ll let you, the reader, do the math for yourself.

 

reharvested L. williamsii

This plant was previously harvested multiple times and the severed crowns sold through the licensed distributors. While the harvesting was conservative enough to not lose the original taproot, this individual strains the concept of “sustainability“. Also notice the steep angle showing careless cutting during two previous harvests.

 

What about the sustainability of harvesting?

Peyote harvesting appears to be a sustainable practice, at least in potential or in theory. In its present-day application however, the slow attrition process leading to the endangered species path has already clearly begun. It is clear that the consumers of peyote still have plenty of peyote to last for some years to come. Maybe even for the rest of our lifetimes, especially if you are middle aged like me.
Sustainability is not something defined by the here-and-now though. A commonly cited definition of sustainability is found in the 1987 Brundtland Report for The United Nations World Commission on Environment and Development, meeting the needs of the present without compromising the ability of future generations to meet their own needs”
As Kimberly Cover pointed out in 2005, that report’s definition is curiously similar to the Iroquois concept of thinking with responsibility for the next seven generations.

Much more study is needed to better define what was seen in the limited harvesting studies that exist but this is how it looks at the moment: The increased rate of mortality that results from a one time harvest is low enough so as not to adversely impact the long term survival of a population. That only appears to be true when adequate time is permitted between harvests. Some period greater than six years is all we can say about that number pending future data emerging. If enough plants of adequate size and potency exist to fill the anticipated needs of the active NAC membership and those plants are being reharvested no more often than they can regrow and return to being what they were prior to the point when they were first cut, harvesting appears to be sustainable.
Anything which creates an average result that achieves less than that, such as is presently the case, is not a sustainable practice.

 

So, let’s come back to our question, “Why ISN’T peyote cultivated?”

Probably the single most important element as to why cultivation is not already a part of the picture is the simple fact that none of the non-NAC people who are legally involved in the supply side have actual legal protection permitting them to cultivate peyote. They are in general law-abiding respected citizens who want to stay out of any trouble. Additionally, the peyote distributors can lose their licenses for violating the law.
As the licensed distributor Mauro Morales told Franks in 2007 . You have to make sure you don’t have a problem with the law, you know?

The portion of South Texas where peyote occurs naturally is commonly referred to as the Peyote Gardens, despite there being a complete lack of historical peyote cultivation. There are presently at least two pertinent stumbling blocks preventing this land from actually being used for creating a real peyote garden (or otherwise addressing the fatal long-term flaws that are inherent within the existing distribution system). Those are located within the Texas DPS (Department of Public Safety) regulations concerning peyote harvesting:

One for the Distributors:
Ҥ13.42. Peyote Distributor Registration. (d) Activity not authorized. A distributor registration does not authorize the distributor to: (1) manufacture or cultivate peyote; (2) ingest or use peyote; (3) deliver to an individual who is an Indian as the term is defined in AIRFA, unless the individual is also an Indian as the term is defined in this subchapter; or (4) import or export peyote except as permitted by federal law.

&
Another for the Ranchers has two pertinent features of interest:

“§13.55 adopted to be effective July 18, 2001, 26 Tex Reg 5266 (only a part is being included below) Nothing in this subchapter affects the ability of a landowner to: […] (2) burn or clear land for purposes unrelated to harvesting, cutting, collecting, or possessing peyote.” and within that same subsection, (b) Prohibited. Unless registered as a distributor or reported to the director as a current employee of a distributor, a landowner may not sell, harvest, cut, collect, transport, or possess peyote. A landowner does not possess peyote in violation of the Act or this subchapter if the peyote is unharvested and growing in its natural state.”

Landowners are permited to charge access fees for peyote harvesting but interestingly there is another clause in this same regulation that adds:
“(d) Harvest fee limitation. Unless the landowner is registered as a distributor, the director will deem the landowner to be selling or distributing peyote if the landowner bases the fee charged or collected under subsection (c)(1) of this section on the amount of peyote harvested, cut, or collected by the Indian using or entering the land”

Notice that this is a dysfunctional “one-price-regardless-of-harvest-size” scenario that actually encourages the maximum possible harvesting to occur per visit. Since the law further sets the retail price as being per piece (i.e. per button) and not by weight there is just as much financial motivation to harvest tiny plants as older ones. Increasing difficulty in gaining access adds additional motivation to maximize the harvests recovered on every visit.

Many ranchers don’t like peyote or peyote harvesting or peyote people and express a familiar bias directed against them. A not untypical attitude is Sahagun’s 1994 quote of ranch owner Robert East. I don’t want them here. That’s all there is to it. I think it’s a dope business, that peyote.” Racism and bigotry often still exist close to the surface in South Texas, in all directions. When talking with ranchers, several times I’ve heard it said that the cause for the disappearance of peyote wasover-grazing by the Indians.”

While that degrading analogy blames the “Indians” there is actually a highly valuable insight if we look at what IS actually real within that notion — namely, as is also true for a rancher’s grazing animals, the NAC is in fact being constrained and provided with its Medicine in a regulated and controlled manner rather than having the freedom to do as they choose. Blaming Native Americans for the, ahem, “over-grazing” problem is about as sound as a rancher blaming their grazing animals for “eating too much” rather than, in this case, correctly recognizing that any “overgrazing” was the direct result of negligent planning, counter-productive activities and incompetent management on the part of the ranch manager.

Similarly the fees charged by ranchers for access are high enough to stimulate maximizing the harvesting per visit as well. Johnson has mentioned ranchers’ greed raising access costs from what once was a pittance to something more significant.

Grant gave a 2000 estimation of it then typically costing $1,500 or $2,000 a month for a peyote lease; which provided a small work crew with access to locate and harvest crowns that were then being sold at the retail level for around $0.15 each.

There is no question that the public perception of the peyote trade being profitable contributed to that increase in peyote lease fees. Not everyone shares completely identical motivations. Sahagun 1994 described rancher Rick Walker as being fed up with trespassers. But he suggested another reason for guarding the peyote gardens on his land. Peyote, he said, may one day become a hot commodity – for ranchers.”

There is at least one rancher in South Texas, the identity of whom is being withheld, who has discovered a unique way to legally make money from his peyote and still protect them from any harm. Instead of leasing his land for the harvest of peyote buttons, he instead “showcases” his peyote plants. He permits organized “eco-tours” to bring visitors onto his property in a bus as part of a fee-based tour. They are allowed to visit his property under tightly controlled circumstances in order to witness and photograph his healthy population of peyote plants. The tour bus also takes the visitors away at the end of the visit so there is no risk of theft.
That population is, just as importantly, also located far enough away from the nearest road to ensure that none of their visitors will be able to return on foot.

While this may sound cynical, one other highly significant factor in the perpetuation of the status quo is that the peyote distributors actually derive a very good living from their trade.

Despite the low cost per button, it is actually a moderately lucrative profession in what is historically an economically depressed region of Texas since the three remaining peyote distributors combined now typically report a total sales of a little under a half million dollars per year ($530,230 in 2013, $434,609 in 2012, $466,590 in 2011, $459,699 in 2010 and $493,834 in 2009 according to DPS records). This reflects their combined totals so in reality it is split into uneven thirds based on how much they actually sell. Each distributor’s total sales pays for their lease fees, their expenses and is also what they pay to the small group of their ’employees’ who help them harvest peyote. In most cases their employees are their relatives.
Unlike the ranches, the distributors are authorized to pay and charge a fee on a per-button basis. Resale prices to their consumers had risen from around $0.09 in 1990 to $0.15 in 2000 and to $0.33 per button in 2011. (A hidden cost factor within that is that the rise in cost had been accompanied by a decrease in size and potency which meant people were required to eat more buttons. See Terry et al. 2012. Link goes to the PDF at CCI’s website.)
A perceived threat to their income and livelihood is no doubt going to be an important motivating factor and can add some illumination to the larger picture and help us to better understand why there is such resistance to change at the distributor level.

Sahagun 1994 quoted Johnson as saying,

I love what I do, enjoy the hell out of it. But hey, you don’t get rich picking peyote.

It is not a huge amount of money but in a region where relatively few other alternative options for similarly lucrative employment opportunities exist it is certainly something that the people involved are going to care about. Relatively few of the distributors and harvesters could successfully turn into peyote growers without investing resources and time in buying land and/or learning skill sets they do not presently possess. Even if they decided to take that path, it would put them on equal footing at the starting gate along with their new competition only if they had the same level of interest, education and skills as a professional gardener or nursery operator.

While the state law that was mentioned previously as granting the distributors their licensing specifically prohibits the distributors from cultivating peyote, the federal law also recognizes that the NAC, or anyone else who is producing peyote for the NAC, has a need to “manufacture” their Medicine (21 CFR 1307.31). [The regulation says “Any person who manufactures peyote for or distributes peyote to the Native American Church, however, is required to obtain registration annually and to comply with all other requirements of law.” That potentially open door for cultivation would apply to any person, NAC or otherwise. There is no special restriction to NAC members in this regulation.] Manufacturing a plant obviously requires growing it or else modern technology has become much farther advanced than I am aware.

Congress has further added an affirmative clause that suggests NAC cultivation was at least being envisioned as enough of a possibility that its regulation needed inclusion.

(b) Use, possession, or transportation of peyote
(1) Notwithstanding any other provision of law, the use, possession, or transportation of peyote by an Indian for bona fide traditional ceremonial purposes in connection with the practice of a traditional Indian religion is lawful, and shall not be prohibited by the United States or any State. No Indian shall be penalized or discriminated against on the basis of such use, possession or transportation, including, but not limited to, denial of otherwise applicable benefits under public assistance programs.
(2) This section does not prohibit such reasonable regulation and registration by the Drug Enforcement Administration of those persons who cultivate, harvest, or distribute peyote as may be consistent with the purposes of this section and section 1996 of this title. (In 42 USC § 1996a.) [Again, this applies to all persons, but it certainly includes the NAC.]

Which, at the very least, suggests that the road to the future cultivation of peyote by the NAC appears to be open as an available option that is protected by federal law. As AIRFAA treats cultivation in exactly the same manner as it does distribution, and because regulated distribution requires a long-standing registration process that functions daily before our very eyes, it would seem to be obvious that Congress intended cultivation to be not merely a hypothetical possibility, but a real option that should be realizable by the act of registration (to be defined and regulated, of course, by DEA).

 

peyote-buttons-Safford-1916

Dried peyote buttons from Safford 1916

 

 

Robledo 2006 included a thought-provoking comment that was left unexplained but touches on an often overlooked contribution to peyote harvesting by the NAC:

Out of the approximate 5 million buttons sold legally each year in the U.S. and Canada, deep South Texas provides about 2 million, with Salvador and his team of peyoteros providing at least 1 million themselves.
What is not mentioned by Robledo is what source provides the other 3 million of those buttons. It is noteworthy that the amount being estimated as procured independently of the activities of the licensed distributors exceeds their total output by 50%. It is reasonable to assume that he refers to the peyote that is being provided by the independent NAC members who are harvesting their own peyote. This brings us to another element in the story that we will return to again later – in the second part of this chapter.
Before moving onward this also is a great example of how much of the current “wisdom” about the peyote trade is based on untraceable rumor rather than documented fact. In the case of Robledo’s intriguing assertion of an actual numeric value for the unregulated peyote trade there are two glaring and inescapable facts that might be easily overlooked: 1) The claim lacks mention of its actual source or providing any indication about where or how this information came into Robledo’s awareness, and 2) it is an absolute impossibility for anyone to keep track of, much less tally with accuracy, the actual extent of the peyote trade occurring independently of the licensed distributors.

 

In 1988, after interviewing the active licensed distributors, John Morthland commented:

Dealers worry constantly about running out of stock, so they keep sources secret from outsiders and even from each other. They are also afraid that if Indians ever discovered the choice growing areas, they might try to bypass the dealers.”

An actual attempt by some peyote distributors to control the peyote trade and deliberately try to prevent cultivation by their customers actually goes back a very long time. Some comments from BIA Special Agent “Pussyfoot” Johnson were featured in an intriguing account by his supervisor that appears in a 1909 issue of the Indian School Journal, entitled “History, Use and Effects of Peyote.”

About twenty-three years ago a white man appeared at Laredo from the Territory in quest of peyotes.
He learned from the Indians up north that in a range of hills about forty miles east of Laredo, these peyotes could be found, He employed Mexicans to gather a supply, which he took north with him. He came in contact with a shipper by the name of Villegas, founder of the house known as L. Villegas and Company. Villegas then began buying these peyotes of ignorant Mexicans and shipping them north to the Indians. This house has been doing this for more than twenty years, but the business has been kept as secret as possible. Villegas has always refused to give the Indians any information as to the source of supply and has also refused all these years to supply Indians with the whole plant, fearing that they would transplant them and thus establish their own source of supply. Half a dozen years ago a member of the firm named Wormser withdrew and established the house of Wormser Brothers, of course taking the secret of the peyotes with him.
These two houses very craftily called these peyotes by the name of Japanese buttons, and created the impression locally that they were for some mysterious use by the Japanese.
These two houses, in this way, have built up a commercial monopoly in peyotes for the whole United States, practically.
About forty miles east of Laredo and four miles from the Texas-Mexican Railway, is an ancient Mexican town of about fifteen families, called Los Ojuelos. It has a graveyard larger than the town itself. It is located close to the edge of some rough, rocky graveled hills, on which these peyotes grow wild; none are cultivated anywhere. They grow wild under the shelter of a bush on these rocky ledges.
[…]
The Mexicans who gather the plant do not pull it up by the roots, but merely cut off the tops, leaving the potato itself in the ground. The top part of this potato then rots. The lower roots then grow and three or four peyotes often thereby appear where there originally was but one. It requires from one to two months’ time properly to dry these peyote tops for the market.
In this village, Los Ojuelos, are two small stores run by V. Laurel and Bro., and the other by Gayetasio Ochoa, the latter being postmaster. The villagers gather these peyotes and turn them into these two stores for supplies, getting about $2.50 a thousand for them. An industrious worker can not gather more than two hundred per day.

 

Modern workers appear to be able to harvest faster.

It used to be you’d go out for a couple of hours and you’d find 500 to 1,000 plants,” he said. “Now, you go out for six hours and you don’t come back with much.
Mauro Morales in Roebuck 2004.

In three hours his two brothers gathered about five potato sacks, some 4000 buttons in all.”
De Cordoba 2004 speaking of his time with Salvador Johnson.

 

Some statistics from the Texas Department of Public Safety (DPS)

Year

# of Buttons

Reported Sold

Total Sales

($US)

Price per Thousand

($US)

Notes

1986 1,913,212 $149,307.52 $ 78
1987 1,766,409 $137,046.30 $ 78
1988 1,575,766 $129,051.01 $ 82
1989 1,572,102 $129,619.62 $ 82
1990 1,772,126 $156.607.29 $ 88
1991 1,859,189 $182,544.02 $ 97
1992 1,886,434 $192,695.25 $102
1993 No data. No data. na [data from DPS in 2005]
1993 1,978,646 $210,247.60 $106 [data from DPS in 2011]
1994 No data. No data. na [data from DPS in 2005]
1994 2,184,739 $246,632.94 $113 [data from DPS in 2011]
1995 No data. No data. na [data from DPS in 2005]
1995 2,252,174 $234,750.20 $104 [data from DPS in 2011]
1996 2,258,993 $278,579.50 $123
1997 2,317,380 $274,500.62 $118
1998 2,076,167 $277,119.71 $133
1999 2,093,335 $335,823.02 $160
2000 2,057,020 $310,722.10 $151
2001 1,934,600 $360,676.00 $186
2002 1,820,847 $422,289.50 $232 [data from DPS in 2005]
2002 1,703,914 $404,859.50 $237 [data from DPS in 2011]
2003 1,779,170 $416,727.00 $234 [data from DPS in 2005]
2003 1,781,170 $416,727.00 $234 [data from DPS in 2011]
2004 1,658,195 $393,572.50 $237 [data from DPS in 2005]
2004 1,304,691 $304,002.50 $237 [data from DPS in 2006]
2004 1,669,806 $393,572.50 $236 [data from DPS in 2011]
2005 1,565,534 $407,789.50 $260
2006 1,619,115 $463,714.75 $286
2007 1,605,345 $474,321.80 $296
2008 1,475,469 $463,148.00 $314
2009 1,604,623 $493,834.00 $308
2010 1,483,697 $459,699.00 $310
2011 1,413,846 $466,590.50 $330
2012 1,106,209 $434,609.00 $393
2013 1,363,978 $530,230.00 $389
2014 1,128,787 $426,300.00 $378

The above reflects the reported activities of the licensed distributors (and their employees) based on figures provided by the Texas Department of Public Safety (DPS).

There are presently three peyote distributors and this has been true since 2006. Four licensed peyote dealers were still in operation in 2003-2005. Prior to that there were five and before that there were more. I have heard that a fourth has submitted his paperwork to DPS. It appears to be a relative of one of the existing distributors who is growing older and facing retirement in the future.

It is an interesting point of clarity that the licensed distributors who sell peyote prefer to be called “peyote dealers” rather than peyoteros.

Math in the fourth column is mine so any mistakes there are mine.

The late 1990s is when the average size plummeted for the buttons showing up in NAC meetings in central Texas. In the late 1990s sacks of Mexican peyote became more common.

 

It is very easy to see that a lot more peyote populations exist in Mexico than are inside of the USA.

The distribution of Lophophora williamsii

map-Anderson-Koehres

The suggested distribution of peyote
Composite map created from Anderson1980 & Koehres

Concerning this map:
It is important to be aware that peyote grows only in soils that are acceptable to it. This is true within any region it occurs, and therefore this map suggests there is a far more substantial distribution and many more populations than really exist (or have ever existed) within the shaded zones.

Anderson created this map by placing the reported herbarium collections, some of which are now known to be erroneous, as dots on a map and then drawing a line encircling them all.
For those reasons reason it is extremely doubtful that any peyote actually lives within large sections of the indicated areas. To put it another way, the presence of a solidly shaded area does not imply a continuous peyote population anywhere within it. It certainly does not indicate a lawn of Lophophora.

Koehres created his map similarly but incorporates his own field information which is superior to that of Anderson.

 

How difficult is peyote to grow?

It is easy to find it said that peyote is difficult or even impossible to grow.

After interviewing peyoteros in 1988 John Morthland wrote,

Indeed, peyote is almost impossible to cultivate. Once a seed germinates, the plant takes five years to grow big enough for picking, and the root of a harvested peyote takes nearly that long to bloom again.

 

Morthland’s “almost impossible” estimates are actually optimistic despite being shorter than reality. A professional cactus cultivator would consider them to be more typical than impossible and would simply take those numbers in stride in his or her production planning.
The reality is that peyote is among the easiest and the most forgiving of the cactus species to grow from seed.

Peyote, like any other cactus species, is fairly slow growing which is why what is developing contains the elements of a crisis-in-the-making. After cultivation begins in a meaningful way, more than a decade can be expected to elapse prior to the first acceptable harvest.

The widely circulated meme that cultivation is somehow either a difficult challenge or an absolute impossibility is probably just simple propaganda that conveniently serves licensed distributors, law enforcement and the powers-that-be alike.
Cactus cultivators have not reported similar results as the image of what is largely Lophophora diffusa in the next photograph should illustrate. These seedlings shown below are growing in Prague.

 

diffusa-in-prague

It is also surprisingly common to find it said that peyote cannot be cultivated anywhere outside of its natural ranges. People like Leo Mercado who, in theory, have proved this to be in error have actually proven just how right Voltaire was when saying:

It is dangerous to be right in matters on which the established authorities are wrong.”

At least, we now understand WHY peyote cultivation is considered to be impossible: not because of any technical issues but rather because the federal, state and/or local police will come and destroy the peyote plants if they learn of their existence.

The Peyote Foundation 1998

The Peyote Foundation 1998

Leo’s “impossible” shade house in 1998.
Taken with Leo’s permission from their newsletter

 

That is only the beginning of this story as it is clear that the cultivation of peyote is easy. Cultivation of someone else’s spiritual sacrament, however, rapidly becomes a quite different subject altogether.
The one very significant hurdle for the cultivation of peyote is a lack of acceptance by more than a relatively few members of the NAC.

This will be explored in more detail when this commentary continues.

 

More is still to come with part 2.

 

Related Reading Off-Site – Cactus Conservation Institute’s website

 

Additional Related Reading Off-Site – Edward Anderson’s thoughts on the Peyote Crisis.

 

Abbreviations used in Sacred Cacti

Areole of Trichocereus pachanot compared to Trichocereus scopulicola

 

A simple listing of the technical abbreviations used in the 4th edition

µm = micrometer = micron

ml = milliliter

Å = angstrom

MLD = minimum lethal dose reported in literature

BCE = before current era

mM = milliMolar

BP = before present

mm = millimeter

bp= boiling point

mmp = mixed melting point

cm = centimeter

mp = melting point

dec. = with decomposition

ms = mass spectroscopy

dm = decimeter (10 cm.)

na = not available/applicable

et al. = et alia (“& others”)

nd = not detected

f = forma

nm = nanometer

ft = foot

nn = nomen nudum (named but lacking any description)

gc = gas chromatography

RT = room temperature

gm = gram

sc = subcutaneous

in = inch

sn = sine numero(lacking a collection number)

im = intramuscular

sp = species (singular)

ip = intraperitoneal

spp = species (plural)

ir = infrared

ssp = subspecies

iv = intravenous

subsp = subspecies

kg = kilogram

TD = toxic dose

kV = kilovolt

TLC = thin-layer chromatography

LD100 = lethal dose 100%

uv = ultraviolet

LD50 = lethal dose 50%

v = volt

mm = millimicron (= nm)

var = variety

m = meter

X = indicates a hybrid

ma = milliamp

MAO = monoamine oxidase

MAOI = mao inhibitor

 

 

Chapter 3; distribution & occurrences

Trichocereus peruvianus P.C.Hutchison 543. (Found at 1700m)
Collected in the canyon of the Río Rímac, Huarochiri Prov., Peru

 

 

The Distribution & Occurrence of Mescaline


This chapter is intended as an overview to set the stage for the next chapter detailing the mescaline containing species. In the work which follows, most taxonomic synonyms were omitted as these are readily available in the sources cited and are primarily only of historical importance. (More detailed and ‘properly’ worded taxonomic descriptions of the plants can be found in the listed references.)

        To better assist the reader in search of more information it was thought helpful to include synonyms that are in horticultural use or used in the references included.

        Many times plants get renamed or transferred by one authority without being accepted by some or most others. In some cases, such as Stenocereus, it is not uncommon to find several different names for the same plant depending on which reference work one consults. While it is unlikely that they would be encountered and still referred to as a Cereus, as many cereoids were originally called, it is just as likely they will not be listed by MOST sources as a Stenocereus.

        Any feedback on how this could be made more useful and accessible is welcomed.

Proviso:

        It must be kept in mind that substantial differences in the alkaloid content and in the relative ratios of alkaloids present have been noted by numerous researchers. (True also in many other families.) These differences have been noted to sometimes appear seasonally, such as the higher presence of N-methylated (as compared to N-demethylated) alkaloids detected, by Lundstrom, during summer in greenhouse maintained peyote. In contrast; in the same population of plants, winter analysis found levels of N-demethylated compounds to be higher than N-methylated ones. [While he used cultivated plants, the mescaline content was comparable to most of what is collected from the wild.]

        They can vary as well according to the age of plant (young plant versus adult plant) or even by age of part (such as new growth on a large adult compared to older growth). In cacti, the actual variables effecting such reports are, usually, unknown and unstudied.

        Alkaloid content has been noticed to vary substantially in amount and/or actual even composition between varieties considered closely related by morphology, and concentrations sometimes vary widely even from one individual or locality to the next. In others even daily fluctuations have been noted; in Phalaris and Papaver, for example, alkaloid concentrations were found to be highest in the early morning. (Quantitative comparative isolations of Phalaris was reported by Appleseed.)

        Very few workers seem to concern themselves with any of this and rigorous work on this subject has rarely been performed or published.
The bottom line is that a published analysis says something about the actual material analyzed by those particular workers and can be reliably extrapolated to mean almost nothing concerning what YOU have or another person possesses. It CAN be valuable as an indication of what molecules might be anticipated but the composition and quantification of alkaloids needs to be determined on YOUR plants in order to know what you actually have. Plants do not read, listen to or follow the publications of scientists.

        [Species suggested by published analysis to be variously weak or potent have on occasion proved to be just the opposite!]

        Often the only data included is whether the plant was cultivated or collected from the wild. In many early papers we literally have to rely on the word of the workers as to the identity of what they analyzed, as vouchers for reference’s sake were never prepared and there is no physical means for confirmation.

        Fortunately, in recent decades, far more attention is being given to the importance of proper herbarium vouchers being prepared for any and all plant analysis. Even in these cases, not all workers note enough variables for their observations to be truly meaningful.

         Critical data for wild plant collections: size and approximate age, part of plant used and stage of growth, i.e. actively growing versus fully developed (if sampling only branches of large specimens), and time of harvest (time of year and time of day) should all be included along with place of origin and elevation of occurrence.

         Ideally for a voucher some comments on the local ecology and a description of habitat would also be quite valuable. This could include the plants growing around it, or with it, the immediate local conditions of occurrence [moisture, degree of sun, etc…], its apparent niche in ecosystem, and a description of the land or terrain.

         Even better would be additionally including a local soil test and/or sample, and analyzing as many parts and ages of material as possible, as well as repeated tests with the same specimens at different times of year.

         If performing repeated samplings of the same individuals; stress can become a factor capable of influencing the results. I suggest initially using pooled smaller samples of adjacent individuals within a given population. There should be additional small samples taken from several individuals within the same population that is pooled in order to check for uniformity and evaluate the degree of potential influence from outliers.

         Most plants can recover rapidly and well from light prunings. A minimum of two years time is suggested for such a series of samplings with a maximum of 6-8 trimmings. Differences in regrowth versus original growth should also be evaluated.

         The factors controlling and regulating alkaloid production would be a fascinating and productive area for future academic research. If chemotaxonomy is to ever be considered a truly useful inclusion in the repertoire of taxonomic tools, science needs to be better able to define the parameters of alkaloid production.

         Determining and taking steps to maximize alkaloid content would also be of benefit for those who view these plants as sacraments. Selection for known high alkaloid strains, or focusing on clones of specific exceptional individuals, for intensive large scale breeding and propagation efforts, would be a worthwhile avenue for everyone involved with sacramental use of these plants.

 

distribution; Opuntia-ficus-indica

a thirsty Opuntia ficus-indica growing in Australia

 

The distribution of mescaline containing species within the Cactaceae

Nonbold face specific names indicate acceptance as a species is still not widely recognized.

Family: Cactaceae

     Subfamily: Cereoideae

        Tribe Pereskieae

Pereskia corrugata 

Pereskia tampicana

          Tribe Opuntieae

Pereskiopsis scandens 

              subtribe Cylindropuntia 

Opuntia acanthocarpa 

Opuntia echinocarpa 

Opuntia imbricata 

Opuntia spinosior 

subtribe Opuntia 

Opuntia basilaris 

Opuntia ficus-indica

          Tribe Cacteae

            subtribe Cactinae 

Pelecyphora aselliformis 

            subtribe Cereinae 

Polaskia chende 

Pterocereus gaumeri 

Stenocereus beneckei 

Stenocereus eruca 

Stenocereus stellatus 

Stenocereus treleasei 

Stetsonia coryne 

Trichocereus bridgesii ***(all forms*)

Trichocereus bridgesii monstrosus *** 

Trichocereus cuzcoensis *** [Often 0.0%. See its entry.]

Trichocereus fulvilanus 

Trichocereus huanucoensis

Trichocereus macrogonus *** 

Trichocereus pachanoi *** 

Trichocereus pachanoi monstrosus

Trichocereus pallarensis *** 

Trichocereus peruvianus *** 

Trichocereus peruvianus monstrosus

Trichocereus puquiensis *** 

Trichocereus puquiensis monstrosus

Trichocereus santaensis *** 

Trichocereus schoenii *** 

Trichocereus scopulicola *** 

Trichocereus sp. W.Baker 5452 ** 

Trichocereus cv. SS01, SS02, SS03

Trichocereus cv. TJG *** 

Trichocereus sp. Torres & Torres: N. Chile

Trichocereus cv. “Unknown C”

Trichocereus sp. aff. huanucoensis

Trichocereus strigosus 

Trichocereus taquimbalensis

Trichocereus terscheckii *** 

Trichocereus thelegonoides 

Trichocereus uyupampensis *** (Erroneous ID)

Trichocereus validus 

Trichocereus vollianus 

Trichocereus werdermannianus *** 

            subtribe Echinocactinae 

Aztekium ritteri 

Gymnocalycium achirasense 

Gymnocalycium asterium 

Gymnocalycium baldianum 

Gymnocalycium calochlorum 

Gymnocalycium carminanthum 

Gymnocalycium comarapense 

Gymnocalycium denudatum 

Gymnocalycium gibbosum 

Gymnocalycium horridispinum 

Gymnocalycium leeanum 

Gymnocalycium mesopotamicum 

Gymnocalycium monvillei 

Gymnocalycium moserianum 

Gymnocalycium netrelianum 

Gymnocalycium nigriareolatum 

Gymnocalycium oenanthemum 

Gymnocalycium paraguayense 

Gymnocalycium quehlianum 

Gymnocalycium ragonesii 

Gymnocalycium riograndense 

Gymnocalycium stellatum 

Gymnocalycium striglianum 

Gymnocalycium triacanthum 

Gymnocalycium uebelmannianum 

Gymnocalycium valnicekianum 

Gymnocalycium vatteri 

Islaya minor 

Lophophora diffusa *** (but not usual case)

Lophophora fricii *** [Does not appear to be typical. May have been an ID error?]

Lophophora jourdaniana *** 

Lophophora koehresii 

Lophophora williamsii williamsii *** 

Lophophora williamsii echinata *** 

Turbinicarpus lophophoroides 

Turbinicarpus pseudomacrochele var. krainzianus 

Turbinicarpus schmiedickianus var. flaviflorus 

Turbinicarpus schmiedickianus var. schwarzii 

 


Please note that this system of organization is presently no longer accepted by most authorities but it is still commonly encountered in horticulture and among ethnobotanists.

        However, an attempt was made by Albesiano & Kiesling in 2011 to resurrect the genus Trichocereus and all of the molecular work to-date indicates that they are on solid ground. See elsewhere in this work for more details.

        Most of the species listed contain only trace amounts.

        Species marked * lack formally published analytical work but have successful human bioassays reported.

        Species marked ** have unpublished analytical work confirming mescaline’s presence as well as successful human bioassays reported.

        Species marked *** have both published analytical work & successful human bioassays reported.

 

distribution; Acharagma-aguirreana

Acharagma aguirreana (Glass & R.Foster) Glass
(Formerly known as Gymnocactus aguirreanus Glass & R.Foster.)
DNA work by Wallace suggests that this may be Lophophora diffusa’s closest relative.
Reported to contain over 2% hordenine by West et al. 1974.


A more recent view

        This is that same list but using the currently accepted names. Species that are missing from this list were variously discarded, merged or ignored in the revisions. Details can be found under their entries.

        One thing that careful readers will notice about this arrangement is that some of the new combinations merge plants with quite different published chemistry. If a plant reported to contain mescaline was renamed as a synonym of one which did not it was omitted from this list.

        I would suggest that these be looked at closer with an eye for possible subdivision into chemical races.

        Comparisons of Anderson, Hunt & others will also rapidly reveal a lack of agreement on a number of points and the seemingly capricious acceptance of some and rejection of others with little if any comment. Hunt’s lack of meaningful references, including in some cases the actual describers, precludes any resolution in a number of instances.

        Some of the combinations are so peculiar as to have caused me to wonder if Anderson and Hunt really actually examined flowering specimens or in some cases ANY actual specimens.

        In several cases, the mergers were published by people who seemingly lacked first-hand examination of the material. For instance the peculiar assertion that the slender, densely branching Trichocereus uyupampensis Backeberg and the stout, solitary columnar Trichocereus validus sensu Backeberg are synonymous.

        When faced with this situation we would suggest to botanists that they should not be afraid to say “I don’t know” or at least search out bona fide materials before uttering such pronouncements in print.

        What is perhaps most fascinating is the movement within the Opuntioidae towards lumpy definitions of the species accompanied by a splitter’s view of the genera.

Family: Cactaceae

    Subfamily: Pereskioideae 

Pereskia corrugata 

Pereskia tampicana

    Subfamily: Opuntioideae 

Cylindropuntia acanthocarpa 

Cylindropuntia echinocarpa 

Cylindropuntia imbricata 

Cylindropuntia spinosior 

Opuntia basilaris 

Opuntia ficus-indica 

Pereskiopsis scandens

    Subfamily Cactoideae 

        Tribe Browningieae 

Stetsonia coryne 

        Tribe Cacteae 

Aztekium ritteri 

Lophophora diffusa 

Lophophora fricii 

Lophophora williamsii 

Turbinicarpus lophophoroides 

Turbinicarpus pseudomacrochele subsp. krainzianus 

Turbinicarpus schmiedickianus subsp. flaviflorus 

Turbinicarpus schmiedickianus subsp. schwarzii 

Pelecyphora aselliformis 

        Tribe Notocacteae 

Eriosyce islayensis 

        Tribe Pachycereeae 

Polaskia chende 

Pachycereus gaumeri 

Stenocereus beneckei 

Stenocereus eruca 

Stenocereus stellatus 

Stenocereus treleasei 

        Tribe Trichocereeae 

Gymnocalycium asterium 

Gymnocalycium baldianum 

Gymnocalycium calochlorum 

Gymnocalycium carminanthum 

Gymnocalycium denudatum 

Gymnocalycium gibbosum 

Gymnocalycium leeanum 

Gymnocalycium mesopotamicum 

Gymnocalycium monvillei 

Gymnocalycium monvillei subsp. achirasense 

Gymnocalycium monvillei subsp. horridispinum 

Gymnocalycium netrelianum 

Gymnocalycium oenanthemum 

Gymnocalycium paraguayense 

Gymnocalycium quehlianum 

Gymnocalycium ragonesii 

Gymnocalycium pflanzii var. riograndense 

Gymnocalycium stellatum 

Gymnocalycium striglianum 

Gymnocalycium triacanthum 

Gymnocalycium uebelmannianum 

Gymnocalycium valnicekianum 

Gymnocalycium vatteri 

Echinopsis lageniformis 

Echinopsis cuzcoensis 

Echinopsis fulvilana 

Echinopsis macrogona 

Echinopsis pachanoi 

Echinopsis peruviana 

Echinopsis peruviana subsp. puquiensis 

Echinopsis santaensis 

Echinopsis schoenii 

Echinopsis scopulicola 

Echinopsis strigosa 

Echinopsis tacaquirensis subsp. taquimbalensis 

Echinopsis terscheckii 

Echinopsis thelegona 

Echinopsis uyupampensis 

Echinopsis volliana 

distribution; Lophophora williamsii echinata
Lophophora williamsii echinata


 

Distribution of alkaloids *within* cacti.

 

    Surprisingly there has been very little serious work published on this topic.

    Alkaloids in “pellote” (i.e. peyote) were reported by JANOT & BERNIER 1933 to be almost exclusively in the internal cells of the cortical parenchyma at top of plant. (See TLC results by Todd elsewhere here.)

    In Trichocereus candicans alkaloids were found by Niedfeld to be mainly in the chlorophyllaceous cortical parenchyma. (Niedfeld used microchemical methods to determine this) RETI 1950 cited NIEDFELD 1931.

    In T. terscheckii; alkaloids are primarily in the parenchymal tissues, 29% were found to be in the green epidermis (dry), while the central parts (dry) including cortical parenchyma contained 45% of the total alkaloid content [please note that this included the vast majority of the parenchymal tissues and the total weight of that portion of the plant is much higher than that of the green epidermis. This indicates a lower concentration for the central parts than in the green portion but potentially useful concentrations nonetheless.] RETI & CASTRILLÓN 1951

    Parenchymal tissues are highly specialized thin-walled storage cells that exist within in the thick outer layer on the plant. They are the site of many metabolic processes and also store such things as water, calcium oxalate crystals and often alkaloids.

    Calcium oxalate crystals are said to be stored in abundance in some peyote specimens. A nice image of showing their presence inside of the flesh of peyote can be found in the entry for Lophophora williamsii.

    As far as I can determine, the parenchymal tissues extend from near the skin to the vascular bundle; including most of the tissues other than vascular, structural or connective.

    Cortical parenchymal tissues are those towards the outside. Chlorophyllaceous just means that they have chlorophyll (are green.)

    Obviously, when a peyote button is sliced into two horizontal portions, they will be slightly more prevalent in the top half of the button than the bottom half of the above ground portion due to the relative percentage of tissue which is occupied by the central vascular tissues and by the outer layer. Published analytical work reflects this (see under Lophophora williamsii chemistry.)

    A similar picture was reported in Kircher 1972 for triterpene glycoside distribution within the flesh of the organ pipe cactus Lemaireocereus thurberi:

Tissue % of total Methanol soluble product
Epidermis 4
Photosynthetic layer 42
Transition zone 28
Cortex 12
Pith 10
Wood 3

       

   As there is considerably more weight to the central parts than the green portion, the observations from RETI & CASTRILLÓN 1951 provide some support to the idea common amoung users that the highest mescaline concentration is within the green tissues on the periphery of the plant.

   Less” does not mean that there is no alkaloid in the whitish tissues beneath it. All evidence suggests that there is ample alkaloid contained in these parts, just significantly less than in the green layer. It is also likely there is even less in the central vascular bundle and core itself.

   Another interesting result was noted among SMOLENSKI and coworker’s multitude of general alkaloid screenings. When testing Pachycereus pecten-aboriginum they reported Roots: ++, Stems: – and Ribs: +++. As slicing off the ribs would remove most of the cortical tissues this is in line with the above observations. Their account provides no further information on tissues evaluated (samples provided to them as a previously prepared extract).

   There is additional support for this; DJERASSI et al. 1953b determined that the majority of the alkaloid content in Lophocereus schottii was in the green epidermis (6.7% crude alkaloid); only a minor portion in the cortex (1.1% crude alkaloid) and almost no alkaloid in the core & pith (0.2% crude alkaloid).
   By cortex Djerassi means the epidermis, by green epidermis Djerassi refers to the chlorophyllaceous parenchyma. Djerassi was a natural products chemist not a botanist.
The casual and nonconsistent use of the words epidermis and cortex has caused confusion for many readers who did not stop and ask what was being actually meant by the user of those particular words and instead translated them based on what they themselves would have meant by those words.]

   Anderson described TODD 1969 as finding little difference [qualitative] between the alkaloids of root and top in peyote except for hordenine which was only present in the root. While true in most aspects, this is a little misleading as concentrations in the roots are far lower than in the tops. Please see more details under the Lophophora williamsii entry. [In Sacred Cacti 3rd ed. Part A or in Sacred Cacti 2nd ed.]

   This is also in at least partial conflict with the reports of other workers.

   Todd collected his samples during June. Curiously, lophophorine was apparently observed as the major alkaloid in L. williamsii. [See also comments on the seasonal fluctuations of alkaloids in peyote.]

   GUTTIERREZ-NORIEGA 1950 (citing CRUZ SÁNCHEZ 1948) appears quoted as saying that the alkaloids are primarily in the “bark” of T. pachanoi. His word, corteza, translated in the English summary as bark, also means ‘cortex’ or ‘skin’ in Spanish.

    Apparently CRUZ SANCHEZ worked with the outer layer due to the slime resulting from use of the whole stem interfering with his extraction procedure. He reported 5% in the dried outer layer.

   This area needs further work. While many alkaloids may indeed be higher towards the outside of the plant there are known exceptions. Hordenine being observed in the root rather than the top (in peyote) is a good example. Its highest concentrations being in the root was reported again in Mammillaria microcarpa by KNOX and coworkers.
It is noteworthy also that all of the alkaloids measured by KNOX were much higher in the cortex itself as compared to the chlorophyll rich tubercles and several were higher in the vascular tissues than in the tubercles.

      An Entheogen Review reader wrote to say that they had found an unspecified amount of the cores of San Pedro to be active but they provided inadequate information for us to understand HOW they actually determined this or how much they observed.

   This should not be any surprise should a person ingest a large enough amount.

   PUMMANGURA et al. 1982 reported that mescaline did not transmigrate between grafted T. pachanoi and T. spachianus regardless of which was used as stock and scion. Their conclusion was that mescaline was locally produced and noncirculating.

   While it may or may not be true that transmigration of alkaloids does not occur, SINISCALCO 1983 reported that the normally mescaline-free Myrtillocactus geometrizans was found to contain 0.3% mescaline by dry weight after having previously been grafted with Lophophora williamsii.

   Many questions immediately arise. None are presently answerable.
Trichocereus scopulicola NMCR

Trichocereus scopulicola FR991 seedling (NMCR); from Ritter’s species but using seed acquired from Riviere de Carault.

In an odd e-mail that I received in 2004, Karel Knize commented

        “Some flowers are used (cont ca 4%) plant itself 2-3.5%
the strongest type are 9-12 ribs or 3-4 ribs
Knize did not elaborate further (and I’d suggest this be taken with a large grain of salt). 

        A friend has claimed to have had good results from the flower masses they collected from peruvianoids and terscheckii but preserved no details.
In more recent years, additional friends ingesting pachanoi and peruvianus flowers and ovary could discern no effects whatsoever.  Clearly some analytical work seems in order to know what to believe.
There IS something that perhaps may be true? In evaluating the reports of human bioassays it is always important to be able to identify and preclude the contributions from any “non-negative placebo responders” (to borrow Jim Ketchum’s wonderful phrase).

        It is almost unbelievable that no one has looked into the matter of alkaloid distribution within cacti more thoroughly.

        The analysis of only the outer green layers and only looking at only mescaline has become the predominate analystical approach. This is for practical reasons not a reflection of a fixation on mescaline.
        The reasons are simple:
1. It is easier to work with the slimy inside of the cactus if only the outer green layer is used.
2. Most researchers would LOVE to look at every alkaloid in their plants but due to a lack of reference materials the necessary standards are simply not available through commercial sources. Out of the 63 alkaloids reported from peyote, for example, only 5 or 6 can be obtained from fine chemical houses.
        Historically workers doing structural analysis would accumulate and save their purified alkaloids. These were then shared with other people doing the same work. When they were still active in research, Jerry McLaughlin & Arnold Brossi were the actual reference standard resources for multiple other workers.
        Synthesis is also possible but the actual cost and ability to create an functional set of basic cactus alkaloids reference standards via synthetic means is out of the reach of the average grad student performing analysis on the alkaloids of a plant. Mescaline, by contrast, is relatively easy to obtain as a pure reference standard so it now tends to be the only target being identified and quantified.

 

 

Trichocereus scopulicola Oz

 

Trichocereus scopulicola grown from seed in Oz. All of these originated as FR991 seed that were acquired from Ritter’s sister Hildegarde Winter but Australian cactus producers have been generating and relying on their OWN domestic seed production from the *plants* that were produced from Winter’s seeds since the 1960s.

 

 

Islaya

Islaya minor Backeberg

Curt Backeberg (1934) Kaktus-ABC 258, as Islaya minor
Carl Friedrich Förster (1861) Hamburger Gartenz, 17: 160, as Echinocactus islayensis.
Fred Katterman (1994) Succulent Plant Research, 1: 117, as Eriosyce islayensis.

Ritter_1981_3_1185_Islaya_krainziana_ill

Image above is from Ritter. I have not been able to locate who owns Ritter’s copyrights so have not obtained permission for the use of this image. If someone can give me more information on how to organize formal permission it is most welcomed or if the presence is objectionable it will be removed promptly.

 

According to Anderson 2001, all of the former genus Islaya has been merged as a highly variable Eriosyce islayensis (C.F. Förster) Katterman.

Mescaline present in trace amounts (0.0017% in dry plant)

Origin: Found in southern Peru (above Mollendo, dept. of Arequipa). [Named for the town of Islaya.]

Habitat: Arid, dry desert regions with little rainfall. Mineral rich alluvial sediments, on sand dunes and exposed windy slopes. Most moisture is derived from fog.

Forms simple (unless apically damaged) short plants up to 13 cm tall and 7 cm wide.

Ribs are 6 mm in height and number around 17. The areoles initially bear whitish-grey felt.
Spines are rigid black, later becoming grey.
There are 20 to 24 six mm long thin radial spines and 4 cruciform (usually) centrals which are stouter, thickened below and up to 18 mm [20 mm] long.
3/4 inch [2-2.2 cm.] flowers arise from the felted area and vary from golden to light greenish-yellow.
Hairy, carmine fruit starts globular and ripens elongated. Perianth and a few bristles persist on the top of the fruit.
Backeberg 1977 page 217.
and Pizzetti 1985 Entry #137. (Pizzetti has a color picture with fruit.)

These are represented in collections as beautiful but small and slow growing specimens.

Backeberg notes that wild collected plants of Islaya are sometimes difficult to grow.

Reported analysis of Islaya

Mescaline was present at 0.0017% in the dry plant. (tlc, gc)
3,4-Dimethoxy-β-phenethylamine present at 0.0038% in the dry plant. (tlc, gc)

 

Also observed but did not quantify (using tlc only):
β-Phenethylamine
Hordenine [N,N-Dimethyltyramine]
3-Methoxytyramine
N-Methyltyramine
Tyramine [4-Hydroxyphenethylamine]
Pellotine [6,7-Dimethoxy-1,2-dimethyl-8-hydroxy-1,2,3,4-tetrahydro-isoquinoline]
Corypalline [7-Hydroxy-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline] (The only reported occurrence of this alkaloid within the Cactaceae)
Doetsch et al. 1980

 

 

 

External links:

Dave’s Garden’s
IPNI
ThePlantList
Tropicos

Disclaimer

Disclaimer & Cautionary Statement to Readers

 

This disclaimer is actually important for you to read. All information is contained strictly for informational and educational purposes and should not be construed as advocacy for anyone to violate state or federal laws. 

Depending on where a person lives, the following material contains discussions of practices that might place one in direct violation of state and federal laws if they were applied in reality by the reader. 

Mescaline and some similar substances are currently regarded as dangerous drugs. 

Despite a complete lack of human fatalities and a proven safety record in humans exceeding that of many commonly prescribed & readily available over-the-counter pharmaceuticals, they are, in fact, at least potentially, quite dangerous substances. This is not due to their their pharmacological or toxic properties but rather is entirely the direct result of the potential actions that may arise from those who quixotically consider them to be dangerous and who are dedicated to MAKING them dangerous. 

These peoples’ extremely serious and ever-present threat of very real danger should never be underestimated. This is not a rational issue for them and no amount of logical persuation can be expected to sway their emotionally and/or religiously based opinions.

Failure to comply with state or federal laws can result in lengthy imprisonment, excessive fines, terroristic home invasions, deliberate terrorism of your family & friends, wanton destruction & vandalism of personal belongings, infliction of immense mental anguish on you & your loved ones, savage beatings & other physical injury, intimidation or harassment of friends or casual acquaintances or even the targeting of them for similar fates, attempted or successful sabotage of career or business reputation with malicious attacks upon and slanderous accusations against personal character being deceptively presented to employers, friends, family or business acquaintances with deliberate pejorative intent, deliberately brutal murder or injury of pets, eviction from rental properties and/or a complete loss of assets, checking & savings accounts, vehicles, computers, other possessions & real property, child custody, or even worse. 

You may even find yourself being shot in the middle of the night by automatic weapons carrying, night-vision goggled home-invaders as you are trying to put on your pants. 

There is no example mentioned above which has not already occurred in the efforts being directed against drug users.

While seemingly unthinkable in any free and democratic society, this is currently the very serious state of reality produced by the present illegality of an increasing number of these substances and the existence of a well-funded and powerful modern-day Inquisition that is dedicated towards our eradication via a brutal reign of terror and violent suppression.  The war on drugs is not really a war on drugs but a war on drug users.

Readers should operate under no illusions when reflecting upon the reality of this as yet another attempted state-sponsored social purge & cultural cleansing.

The information contained in these pages is intended to better enable future research into this important and fascinating area of consciousness and science.

We do not advocate the use of illicit —or for that matter, any— drugs by uninformed or underinformed individuals.

However, we also recognize that many people will choose to use drugs whether they are informed or not.

We do not intend to encourage or promote drug use. 

We do want those who are already determined to use these substances, regardless of current legal status, to be able do so in an informed, knowledgeable and responsible manner; whether this is planned as sacrament, ‘recreation’ or experimental material.

Our hopes and intentions are that, through education and awareness, more informed choices can be made, thereby minimizing the risks often associated with substance use.

    It is with this in mind that we present the following.