Cucurbita palmata
Cucurbita okeechobeensis
coyote gourd, coyote gourd or melon, coyote melon
okeechobee gourd
prostrate, often rooting adventitiously at nodes, to 2 m, villous-hirsute to hispid-hirsute with deflexed hairs, glabrescent and muriculate on angles in age;
tendrils mostly 3(–5)-branched 1–1.5 cm above base, retrorsely hispid, gland-tipped.
petiole (2–)3–7 cm, densely hispid-hirsute with short, deflexed hairs mixed with pustulate hairs;
blade suborbiculate to depressed-ovate, palmately 5-lobed, sinuses 1/2–2/3 to petiole, 3–7 × 4–10 cm, usually broader than long or equally so, base cordate, lobes lanceolate-acuminate to triangular or triangular-lanceolate, sometimes irregularly sublobed, margins remotely crenate to remotely serrate-crenate, surfaces appressed-hispid abaxially and muriculate, hirsute-strigillose to hispid-strigose adaxially, midvein and major veins whitish adaxially from densely hispidulous-strigillose with white hairs, eglandular.
in fruit shallowly 5-ribbed, not abruptly expanded at point of fruit attachment, 3–8 cm, spongy.
hypanthium cupulate to campanulate, 2–7(–20) mm;
sepals linear-subulate, 2–10 mm;
corolla golden yellow to yellow, tubular-campanulate, 2.5–5 cm;
anther filaments glabrous;
ovary densely pubescent.
dull white, ovate to oblong, 9–14 mm, margins thickened-raised, surfaces smooth or slightly rough.
dull green, narrowly 10-striped and white-mottled, ellipsoid-globose to globose or depressed-globose, 7–10 cm, smooth.
= 40.
Cucurbita palmata
Cucurbita okeechobeensis
Some plants of Cucurbita palmata from Baja California and California have uniformly whitish gray, hirsute-strigillose adaxial leaf surfaces; these have been recognized as C. californica. Most plants from Arizona and eastern San Bernardino County, California, and some from elsewhere in Baja California and California, have the midrib and major veins whitish like those of C. digitata.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
Subspecies 2 (1 in the flora).
Cucurbita okeechobeensis originally was common in extensive pond-apple (or custard-apple, Annona glabra) forests on the southern shore of Lake Okeechobee (J. K. Small 1922). By the time it was described in 1930, most of these forests had been destroyed. Currently C. okeechobeensis is known only in two population systems Decline and current rarity of Cucurbita okeechobeensis has resulted mostly from conversion of swamp forests to agriculture and from water-level management in Lake Okeechobee. Fluctuations in lake level are necessary as high levels facilitate dispersal, and the inundation and withdrawal create open habitats for quick growth of the seedlings. Exotic vegetation around the edges of the lake, especially Melaleuca, also is a threat.
Cucurbita okeechobeensis subsp. martinezii (L. H. Bailey) Andres & Nabhan ex T. Walters & D. S. Decker (C. martinezii L. H. Bailey) is widespread in a narrow strip of eastern Mexico (Chiapas, Oaxaca, Puebla, San Luis Potosí, Tamaulipas, Veracruz), often in riparian vegetation and as a weed in coffee and citrus plantations. Subspecies okeechobeensis is morphologically distinct only in its densely pubescent staminate hypanthia and pubescent pistillate ovaries. There is no sterility barrier between the two, and F1 hybrids are fertile (R. W. Robinson and J. T. Puchalski 1980). There is considerable allelic variation within subsp. martinezii (T. C. Andres and G. P. Nabhan 1988) but little or none in subsp. okeechobeensis.
R. W. Robinson and J. T. Puchalski (1980) found through isozyme analysis a single allelic difference between the Okeechobee and Martinez gourds. T. W. Walters and D. S. Decker (1991) confirmed the minor allelic difference and estimated the time of divergence as
about 450,000 years, with the conclusion that the two were appropriately treated as conspecific. A population of Cucurbita okeechobeensis was recently discovered in the Dominican Republic (B. Peguero and F. Jiménez 2005); the authors were unable to assign the plants to either subspecies and it is unclear whether the population is natural or the result of introduction within the last century (M. Nee, pers. comm.).
The closest relative of Cucurbita okeechobeensis and C. martinezii appears to be C. lundelliana L. H. Bailey (T. C. Andres and G. P. Nabhan 1988), which is geographically isolated in the Yucatán Peninsula but can form artificial hybrids with them. Cucurbita lundelliana differs in its orange corollas, less lignified exocarp, and seeds with crenulate margins.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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