Colpothrinax wrightii Schaedtler, Hamburger Garten- Blumenzeitung 31: 160 (1875)

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Distribution

Map uses TDWG level 3 distributions (http://www.nhm.ac.uk/hosted_sites/tdwg/geogrphy.html)
Southwestern Cuba and the nearby Isle of Youth (formerly Isle of Pines), O-ca. 200 m; semidry savannas and grasslands (formerly pine forests) on white sand. (R.J. Evans, Monograph of Colpothrinax. 2001)A

Discussion

  • Colpothrinax wrightii is characterized by its swollen trunk. This feature, in combination with its costapalmate leaves, distinguishes C. wrightii from all other Cuban palms. The only other Cuban "pot-belly" palm, Gastrococos crispa (Kunth) H. E. Moore has pinnate leaves. Within Colpothrinax, the small fruits and seeds of C. wrightii are also diagnostic, as are the clear line of abscission at the base of the deciduous corolla lobes and the relatively long stamen-cup. The deciduous corolla lobes and long stamen-cup of C. wrightii flowers are also characteristics of the flowers in Pritchardia, suggesting these to be the ancestral Colpothrinax states and therefore the persistent corolla lobes and short stamen-cup of C. aphanopetala and C. cookii flowers are derived. Charles Wright collected plants for Asa Gray at Harvard University, throughout the island of Cuba, during the years 1856--1867 (Howard 1988). In September 1865 or 1866, he collected a palm (Wright 3964) known locally as "palma barrigona" in the Vuelta Abajo area of western Cuba. A specimen of this palm was sent to Hermann Wendland, Director of the Royal Gardens in Herrenhausen, Germany for determination. Apparently, Wendland considered this palm to belong to a new species and genus and informally assigned to it the name Colpothrinax wrightii. Wright was given this information, and he, in turn, forwarded it to Francisco Sauvalle, a rich landowner and amateur botanist. Sauvalle included the name (attributing it to Wendland and A. H. R. Grisebach) without description, along with the local Cuban name, in his Flora Cubana (1871) [entry 2382 (2381 in the 1873 edition)]. This list was essentially an update and revision of Grisebach's Catalogus Plantarum Cubensium (1866) that incorporated new taxa collected by Wright during his last two years in Cuba, and not seen by Grisebach. Subsequently, O. C. de Kerchove de Denterghem also used the name Colpothrinax wrightii in his Les Palmiers (1878), but again without description. The genus Colpothrinax was not formally established until the following year (Wendland 1879), and the first valid publication of Colpothrinax wrightii (misspelled as "wightii") did not appear for another 16 years (Siebert and Voss 1895). Although Siebert and Voss ascribed the name to Grisebach and Wendland, they cited no specimens as the basis for their description. Quite possibly they never saw a specimen, their description being based solely on information provided by Wendland and/or Grisebach. The most likely specimen they might have seen was formerly deposited in the Krug and Urban Herbarium in Berlin, where both Siebert and Voss resided at the time of their publication of Colpothrinax wrightii. Although this specimen was destroyed, it was photographed by Beccari (photo at BH, which indicates the negative as being at FI-B). Andreas Voss was formerly University Gardener at G6ttingen (1882-1890), so he potentially could have seen the specimen of Wright 3964 in Wendland's herbarium in nearby Herrenhausen. However, there are no annotations by either Siebert or Voss on any known extant specimens of Wright 3964 (nor on the sheets photographed at B). Therefore, unless new information becomes available that clearly demonstrates Siebert and Voss based their description on Wright 3964 at B, or GOET (where the Wendland Herbarium is now housed), or some other herbarium (it is certain they did not see the sheets of Wright 3964 kept by Gray at Harvard University), lectotypification is not possible. Therefore Glassman's (1972) designation of the GH specimen as type is interpreted as neotypification. (R.J. Evans, Monograph of Colpothrinax. 2001)A

Biology And Ecology

  • The climate where C. wrightii occurs is classified as dry tropical (Borhidi 1996). The area has a 5-6 month dry season with an annual precipitation of only 750-1,600 mm. However, during the rainy season (approximately April to September) some lands are periodically inundated (Zona et a1. 2000). Colpothrinax wrightii originally occurred on white sand in open pine (Pinus tropicalis Morelet) forests, in association with the understory palm Acoelorraphe wrightii (Griseb. & H. Wend1.) H. Wend1. ex Becc. (Borhidi 1996). These forests have now virtually all been converted to savannas or pastures as a result of logging and subsequent burning and/or grazing. It was usually the pines in the original forest that were targeted by loggers. (R.J. Evans, Monograph of Colpothrinax. 2001)A

Conservation

  • Despite the elimination of its natural habitat and its exploitation C. wrightii has continued to survive in populations of scattered individuals in the shrub and grasslands and the species was recently given special protection regulating its use (Moya and Leiva 2000). (R.J. Evans, Monograph of Colpothrinax. 2001)A

Common Name

  • Barrigona, palma barrigona ("pot-bellied palm"), palma barrigona de la Vuelta Abajo [to distinguish from (palma) barrigona de sierra, Gastrococos crispa (Kunth) H. E. Moore, another Cuban endemic] (Sauvalle 1871, 1873; Roig y Mesa 1928). (R.J. Evans, Monograph of Colpothrinax. 2001)A

Uses

  • C. wrightii has also been much exploited locally, the swollen "pot-belly" of the trunk being used for such things as water containers, furniture, and even beehives (Alain 1961; Moya & Leiva 2000). Non-destructive uses include removing leaves for thatching and gathering fruits for feeding pigs (Moya & Leiva 2000; Zona et a1. 2000). (R.J. Evans, Monograph of Colpothrinax. 2001)A

Description

  • Trunk 6-12(-15) m tall, erect, 15-20 cm dbh, swollen beginning 2-3 m above ground, 30-40(-50) cm diam., naked; trunks of juveniles less than ca. 3-5 m tall usually enclosed in a mat of persistent leaf-sheath fibers, 5-10 cm thick. Leaves usually 10-20; petiole ca. 1-1.5 m long, 3.7-4.6 cm wide at attachment to blade; sheath glaucous, disintegrating and fraying into a coarse, fibrous, nonpendulous network, the individual fibers somewhat serpentine and twisted, typically compressed, 0.6-0.8 mm broad; hastula elevated above the blade, 1.7-2.8 x 4.8-5.8 cm, 2.1-2.8 times as wide as long, depressed to very depressedtriangular, obtuse and ± notched apically; costa 19.5-25.0(-38.5) cm long; blade 142-171 cm long centrally, 39-44 cm long laterally, divided into single-fold segments; central division to within 76-111 cm of (1/3-1/2 to) base, the lateral-most division extending to within 1.5-2.5(-3.5) cm of (> 90% to) base; folds per blade half 36-45; widest single-fold segment 3.4-5.0 cm wide. Inflorescences with flowers and fruit to ca. 5, plus ca. 10 marcescent per individual; primary axis ca. 1.5 m long; inflorescence bracts lanate, with trichomes 2-3 mm long; peduncle ca. 0.4 m long; prophyll ca. 20 x 5 cm; peduncular bracts ca. 6, 22.0-54.5 cm long; rachis bracts 10.5-65.5 cm long; firstorder branches 6-10; axes creamy yellow initially, becoming orange in fruit, their primary-axes 3.073.0 cm long, with unbranched proximal portion 2.0-54.5 cm long, the branched distal portion 1.0-27.0 cm long; prophyll 8.5-44.5 cm long; rachillae typically 20-50 per basal first-order branch, < 10 per apical first-order branch, 3.5-17.5 cm long, tomentose, the trichomes whitish (to ferruginous), 0.4-0.5 mm long; flower-bearing spurs 0.2-0.4 mm long, the subtending bracteole 0.8-1.7 mm long, 0.5-0.9 mm wide basally. Floral receptacle 0.8-1.2 mm long; calyx 2.3-3.3 mm long, free distally from corolla for 1/4-1/2 its length, yellow, with lobes 0.2-0.7 mm long; I corolla 5.3-6.2 mm long, yellow, the lobes valvate, with parallel sides and mucronulate apices, fleshy, adaxially furrowed with involute or thickened margins, forming a hood apically, deciduous, with a clear line of abscission; filaments 3.2-4.5 mm long, connate basally for 2.0-2.7 mm (1/2-3/4 their length), stamen-cup much longer than calyxcup, 1.5-2.7 mm diam., anthers 2.2-3.9 x 0.8-1.2 mm; pollen 30-40 x 25-35 pm, tectum on nonapertural face foveolate; gynoecium 3.5-4.9 x 1.2-2.0 mm, carpels 1.1-1.6 x 0.7-1.3 mm, styles 2.2-3.4 mm long. Fruit 1.1-1.6 cm diam. Seed 0.7-0.9 x 0.9-1.1 cm. (R.J. Evans, Monograph of Colpothrinax. 2001)A

Materials Examined

  • CUBA. Cienfuegos. Harvard Botanical Garden, Soledad, Bailey 12366 (BH), 12367 (BH), Jack 8269 (BH, GH, US), Moore 6092 (BH). La Habana. Isla de Pinos [Isla de la Juventud], San Pedro, Britton & Wilson 14548 (BH, NY, US); Isla de Pinos, near Nueva Gerona, Curtiss 364 (BH, GH, K, MO, NY, US).Pinar del Rio. Consolacion del Sur, Bailey 12504 (BH), Bailey 12504x (BH), Bailey 12516 (BH), Roig s.n. (BH); vicinity of Herradura, Britton et al. 6464 (NY); between Pinar del Rio and Coloma, Britton et al. 9675 (K, NY); Herradura, van Hermann 301 (NY), Leon 14651 (GH), Leon 15934 (GH), Shafer 424 (BH, NY); near Consolacion del Sur, Moore 6807 (BH). (R.J. Evans, Monograph of Colpothrinax. 2001)A