Claviceps paspali
and the Eleusinian kykeon
A correction
Francesco Festi, Giorgio Samorini
The Entheogen Review, 8/3, pp. 96-97, 1999
In the second chapter of the book The Road to Eleusis (Wasson et
al. 1978) Albert Hofmann answered to the question promoted by R.G. Wasson
about the possibility that the old Greeks would have been able to isolate an
hallucinogen from ergot, capable to induce an experience comparable to the experiences
produced by psilocybin or LSD.
The Hofmann's positive answer was articulated on three hypothesis: the first
and the third ones conjectured the separation from Claviceps purpurea
[Clavicipitaceae] parasiting respectively wheat and barley or the infestant
Lolium temulentum L. [Gramineae] of the water-soluble psychoactive
and no-toxic alkaloids (belonging to the ergonovine group) from those responsible
of the gangrenous and/or convulsive syndroms (belonging to the ergotamine-ergotoxine
group).
The second hypothesis, perhaps more suggestive and renowned, supposed the integral
use of Claviceps paspali Stevens et Hall, whose sclerotia appear to exclusively
contain the psychoactive water-soluble alkaloids. The host species ipotetically
individuated by Hofmann was Paspalum distichum L., which "grows
commonly all around the Mediterranean basin and is often infected with Claviceps
paspali" (Hofmann 1978: 31).
After a closer examination of the data on the corology of the Paspalum
genus, this second Hofmann's hypothesis needs a correction, due to an ethnobotanic
oversight, already forecasted by Rätsch (1998: 643).
The genus Paspalum, including 250 to 450 species - depending by the
author - is spread in tropical and subtropical areas of the Old and overall
the New World. In fact, less then 10% of the species is native of Africa and/or
Asia. No one species is indigenous of Europe, where the following species are
present today (Clayton 1980: 263; Conert 1998: 36-37; Garbari 1972; Häfliger
& Scholz 1985: 94-109):
- P. dilatatum Poiret in Lam. [=P. pratense Sprengel, P. ovatum
Nees von Esenbeck ex Trinius, P. lanatum Sprengel, Panicum dilatatum
(Poiret) O. Kuntze, Digitaria dilatata (Poiret) Coste]; it originally
came from South America (Argentine and Brasil); sometimes it is cultivated as
fodder, became wild or naturalized (in wet and shady uncultivated lands) in
Portugal, Spain, Azores, Italy, Austria, and Germany.
- P. urvillei Steudel, original from South America, naturalized in
rice-fields and wet places of Portugal, but very likely to be found in other
countries of Southern Europe.
- P. paspalodes (Michaux) Lamson-Scribner [=P. distichum auct.
non L. Digitaria paspalodes Michaux, P. digitaria Poiret, P.
michauxianum Kunth, P. distichum var. digitaria (Poiret) Hackel,
P. distichum subsp. paspalodes (Michaux) Thellung], original from
tropical areas of America, cultivated as fodder mainly in subtropical countries,
by this time subcosmopolite and still expanding (as example, it became spontaneous
in Cornwall the seventies of this century; cfr. Sell & Murrell 1996: 239); naturalized in Portugal, Spain, Azores, Italy, France, Austria, Germany, Great
Britain, Albany, Bulgary, Greece, Turkey, and European Russia.
- P. racemosum Lamarck, original from Peru and Ecuador, became wild
in Germany.
- P. vaginatum Swartz [=P. tristachyum Leconte, Digitaria
tristachya (Leconte) Schultes, P. inflatum A. Richard, Panicum
vaginatum (Swartz) Grenier & Godron, Digitaria vaginata (Swartz)
Bubani], original from tropical America and (verisimilarly) from tropical Asia,
it has been reported on sea-sands and rice-fields of Portugal, Spain, Italy,
France, and Germany.
- P. quadrifarium Lamarck (=P. ferrugineum Trinius), original
from southern America, adventitious in Italy.
- P. lentiferum Lamarck (=P. curtisianum Steudel, P. glaberrimum
Nash, P. tardum Nash, P. kearneyi Nash, P. amplum Nash),
original from USA and recently reported as adventitious in Germany.
Concerning the particular species reported by Hofmann, it has to be underlined
that the most part of taxonomists consider P. distichum L. a nomen
ambiguus, that is a name that is not possible to refer with sureness to
any known species, while preferring the binomium P. paspalodes (Michaux)
Lamson-Scribner. Observing the above-mentioned list, P. paspalodes is
now the most widespread species of Paspalum in Europe, and the only one
reported in Greece. Nevertheless, also for this species, like for other Paspalum,
its diffusion has to be seen in recent times and however, in the farest hypothesis,
many years after the Conquest. Indeed, considering the dates of the first reports
in the neighbouring countries (for example, in Italy no one species of Paspalum
has been observed before 1900; cf Fiori, 1923-1925, Garbari, 1972), the presence
of Paspalum spp. in Greece cannot be dated before the past century.
It is therefore possible to state with sureness that all the Paspalum
species, which originated from the New or the Old World, spread in recent times,
due to voluntary or not voluntary action by man: because originally cultivated
as fodder then became wild, or because imported and spread together other cultivated
seeds (for example fodders and cereals). On the basis of these data the presence
of P. paspalodes and any other species of Paspalum in old Greece
has to be excluded.
Furthemore, the insubstantiality of the second Hofmann's hypothesis about the
preparation of the kykeon with ergot, is supported by the fact that Claviceps
paspali is an ergot which exclusively infect graminaceous plants of the
Paspalum genus (Grasso 1955), and its presence in Europe is linked to
the recent spreading of its host plants. It's enough to consider that the presence
of C. paspali in France has been reported for the first time only in
1991 (Raynal 1996), and that Greek phytopathologists seem to exclude the presence
of C. paspali today in Greece (Aaronson 1989: 252). Again, in Italy Paspalum
dilatatum has been introduced in 1929 and appeared to be free from ergot
until 1948 (Tonolo 1965).
Beside the botanic-corological considerations here exhibited, a symbolic-iconographic
argumentation could be taken in consideration. The ergot hypothesis of the Eleusinian
kykeon is supported also by the frequent representations of cereals in the iconography
associated to the Eleusinian Mysteries. All the above-mentioned species of Paspalum
have an appearance strongly different from that of the cereals cultivated for
human alimentation; P. paspalodes has an inflorescence constituted by
two (rarely more than one) thin spikes at the top of the stem. It could appear
strange that such characteristic shape would have not found place among the
Eleusinian images. Nor we may believe to a hidden link between cultivated cereals
and Paspalum, verified the species of this last genus have a strongly
different ecology (rice apart) and are not infestants of the cultivated fields
spread during the Classic Greece.
However and in conclusion, we want to underline that the reduction of the possibilities
proposed by the Swiss chemist does not reduce the possibility of the ergot hypothesis.
Hofmann himself stated concerning this: "I mention it only as a possibility
or a likehood, and not because we need P. distichum to answer Wasson’s
question" (Hofmann 1978: 33). All this will be examined with more details
inside an article in publication (Samorini 1999).
References
Aaronson S., 1989, Fungal parasites of grasses and cereals: their rûle as food or medicine, now and in the past, Antiquity, 63:247-257.
Clayton, W.D., 1980, Paspalum. In Tutin, T.G., V.H. Heywood, N.A.
Burges, D.M. Moore, D.H. Valentine, S.M. Walters & D.A. Webb (Eds.), 1980,
Flora Europaea, Vol. V, Cambridge, N.Y., New Rochelle, Melbourne, Sydney,
Cambridge University Press.
Conert, H. J., 1998, Poaceae (Echte Gräser oder Süßgräser). In Hegi,
G., Illustrierte Flora von Mitteleuropa. Band I, Teil 3.
Fiori, A., 1923-1925, Nuova Flora analitica d'Italia, 2 Voll., Tipografia
Ricci, Firenze, Ristampa anastatica: 1974, Edagricole, Bologna.
Garbari, F., 1972, Il genere Paspalum L. (Gramineae) in Italia. Atti
Soc. Tosc. Sc. Nat. Mem., Ser. B, 79: 52-65.
Grasso V., 1955, Rassegna delle specie di Claviceps e delle loro piante
ospiti, Ann.Sperim.Agr.N.S.Roma, 9(I), Suppl. li-lxxxix, Suppl. pp.
XCVII-CXII.
Häfliger, E. & H. Scholz, 1985, Graminacee infestanti. Erbe infestanti
della sottofamiglia Panicoideae. Vol. 1., Cyba-Geigy Edizioni.
Hofmann, A., 1978, A challenging question and my answer. In Wasson, Ruck
& Hofmann, op. cit., pp. 25-34.
Rätsch C., 1998, Enzyklopädie der psychoaktiven Pflanzen, Aarau, Schweiz,
AT Verlag.
Raynal G., 1996, Présence en France de Claviceps paspali Stev. et
Hall. sur Paspalum distichum L. et de l'ergotisme correspondant sur
le bètail, Cryptog.Mycol., 17(1):21-31.
Samorini G., 1999, A contribution to the discussion of the psychopharmacology
of the Eleusinian Mysteries, Eleusis, in publication.
Sell, P. & G. Murrell, 1996, Flora of Great Britain and Ireland. Vol.
5. Cambridge, N.Y., New Rochelle, Melbourne, Sydney, Cambridge University
Press.
Tonolo A., 1965, Sul probabile significato della presenza di alcaloidi negli
sclerozi naturali di Claviceps paspali, Giorn.Bot.It., 72:27-30.
Wasson, R.G., C.A.P. Ruck & A. Hofmann, 1978, The road to Eleusis. Unveiling
the secret of the Mysteries (Ethno-mycological Studies No. 4). Harcourt
Brace Jovanovich, N.Y. & London.