Attalea is a large genus of palms native to Mexico, the Caribbean, Central and South America. This pinnately-leaved, non-spiny genus includes both small palms lacking an aboveground stem and large trees. The genus has a complicated taxonomic history, and has often been split into four or five genera based on differences in the male flowers. Since the genera can only be distinguished on the basis of their male flowers, the existence of intermediate flower types and the existence of hybrids between different genera has been used as an argument for keeping them all in the same genus. This has been supported by recent molecular phylogenies.
Between 29 and 67 species are recognised in the genus, with estimates of as many as 100. Incomplete herbarium collections make it difficult to determine whether certain groups represent single species, or groups of similar species. Attalea species have a long history of human use, and include economically important sources of palm oil and fibre. Many species are fire tolerant and thrive in disturbed habitats. Their seeds are animal dispersed, including some which are thought to have been adapted for dispersal by now-extinct Pleistocene megafauna.
Description
Detail of the crown of Attalea maripa showing leaf arrangement and inflorescences
Attalea is a genus of non-spiny palms with pinnately compound leaves—rows of leaflets emerge on either side of the axis of the leaf in a feather-like or fern-like pattern. Species range from large trees with stout stems up to 30 metres (98ft) tall to acaulescent palms (ones which lack an aboveground stem).[2] The number of leaves per individual varies from about three to thirty-five; larger plants tend to have more and longer leaves.[2]
Inflorescences are large, branched and borne among the leaves.[2] The inflorescence consists of a main axis—the peduncle and the rachis—and a series of smaller branches, the rachillae. The rachillae, which bear the flowers, emerge from the rachis. The peduncle is the main stalk, connecting the rachis with the stem.[3] Inflorescences either consist entirely of male flowers, or are predominantly female with a few male flowers.[2] Fruit usually have two or three seeds, although fewer or more are present in some species, and are usually brown, yellow, orange-brown or purple when mature.[2]
Four different types of male flowers exist. On the basis of these flower types, the genus has often been split into four genera—a more narrowly defined Attalea, Orbignya, Maximiliana, and Scheelea.[2] The species sometimes referred to Orbignya have coiled anthers, while the other groups have straight ones. The petals of those placed in Maximiliana are much shorter than the stamens, while those placed in Scheelea and a more narrowly defined Attalea have petals that are longer than the stamens.[3] Five species do not fit easily into any of these groups; this fact has been used as an argument in favour of considering this group a single genus.[3]
Disagreement exists as to whether Attalea should be considered a single genus, or a group of related genera. In their 1996 Field Guide to the Palms of the Americas, Andrew Henderson, Gloria Galeano, and Rodrigo Bernal combined all the species in the subtribe Attaleinae (as it was then defined) into a single genus, Attalea. In his 1999 Taxonomic Treatment of Palm Subtribe Attaleinae, American botanist Sidney F. Glassman divided the group into five genera—a more narrowly defined Attalea, Orbignya, Maximiliana, Scheelea and Ynesa,[3] although he thought it likely that Ynesa colenda, the only member of that genus, was actually a hybrid.[8]Rafäel Govaerts and John Dransfield recognised a single genus in their 2005 World Checklist of Palms,[9] and Jean-Christophe Pintaud continued this usage in his 2008 review of the genus.[3]
The multigenus approach is based solely on the structure of the male flowers; no other characters could be consistently associated with one genus or another.[10] Four of the genera—Attalea (in a narrow sense), Orbignya, Maximiliana and Scheelea—correspond to four different types of male flowers found within the genus. However, a few species have flowers that are intermediate between these four types, including A.colenda (which Glassman placed in its own genus, Ynesa) and this has been used as an argument for the single-genus approach. The fact that there are several hybrids between species that would be considered different genera under Glassman's five-genus system was also used as an argument for placing them in a single genus.[3] Molecular phylogenetic work by Alan Meerow and colleagues concluded that multi-genus approach did not produce monophyletic groups, but treating Attalea as a single genus did.[6]
Cintia Freitas and colleagues identified three main clades within the genus based on the nuclear WRKY gene family. The first of these, a group of species from the coastal Atlantic Forest region in Brazil all of which had been placed in Attalea in the narrow sense, was termed the Attalea-like clade. This group was a sister to the other two clades. The second group, which they called the Scheelea-like clade, consisted of most of the species formerly placed in Scheelea, together with several that had been placed in Attalea (narrowly defined) and Orbigyna. The third group consisted mainly of species formerly placed in Orbigyna and Maximiliana; they called this the Orbigyna-like clade. Despite the existence of three well-supported clades, Freitas and colleagues concluded that the concept of Attalea as a single genus was best supported by their evidence.[6]
Experts disagree about the number of species in the genus Attalea (broadly defined). In 1965, Dutch taxonomist Jan Gerard Wessels Boer estimated that as many as 100 species may be in the genus. In their 1996 Field Guide to the Palms of the Americas Andrew Henderson and coauthors recognised 29 species in the genus, while Sidney Glassman recognised 65 species in his 1999 treatment of the group. Largely following Glassman's lead, Rafaël Govaerts and John Dransfield recognised 67 species in their 2005 World Checklist of Palms. An important element of this disagreement is the decision by Glassman to define species more narrowly than Henderson. As a result, what Henderson interpreted as variation within species, Glassman took as differences between morphologically similar species. This problem is complicated by the fact that many of these species are poorly represented in herbarium collections. The large size of the leaves, inflorescences and fruit of many Attalea species makes them difficult to collect. In addition, many important collections, including type specimens, have been lost or destroyed.[3] Sparse or incomplete collections make it difficult to differentiate variation within a single species from variation between different species.[3][10] Taxonomic uncertainty is exacerbated by frequent hybridisation between species.[6]
The three recent treatments (Henderson and coauthors, Glassman, and Govaerts and Dransfield) recognised a total of 73 species, but only 20 species are accepted by all of them. The remainder account for either nine species or more than 40. For example, what Andrew Henderson considered a single species, Attalea attaleoides,[17] other authors have considered a species complex consisting of four or five species. Glassman doubted the validity of A.attaleoides as a species, and described four new species from material that had previously been attributed to A.attaleoides—A.camopiensis, A.degranvillei, A.guianensis and A.maripensis. Govaerts and Dransfield accepted both Glassman's four species and A.attaleoides. However, Jean-Christophe Pintaud was of the opinion that A.guianensis, A.maripensis and A.attaleoides were all very similar, and thought it likely that they all represented the same species.[3]
Another species complex in Attalea includes A.speciosa and related species. Henderson (1995) recognised A.speciosa and A.spectabilis, considering the latter to either be an acaulescent form of A.speciosa or a hybrid between A.microcarpa and it. Govaerts and Dransfield accepted A.spectabilis, but Glassman considered it a dubious taxon. Attalea vitrivir was recognised as a distinct species by Michael Balick and coauthors;[18] Glassman and Govaerts and Dransfield concurred, but Henderson considered it part of A.speciosa. Glassman also described a fourth member of this group, A.brejinhoensis, and it is accepted by Govaerts and Dransfield.[3]
Reproduction and growth
Male inflorescence of Attalea sp. swarming with insects.Attalea sp. – MHNT
Attalea species are monoecious—male and female flowers are separate, but are borne by the same plant.[2] Various species have been described as being insect-pollinated, including A. phalerata,[19] while pollination in A. colenda and A. speciosa, has been attributed both to insects and wind.[20][21] The fruit are animal-dispersed.[2]
Seed germination is remote tubular[22]—during germination, as the cotyledon expands it pushes the young shoot away from the seed.[23] After germination, the stem initially grows downward before turning to grow upward and produce the aboveground stem.[24] This produces a "saxophone shaped" belowground portion of the stem.[25] The fact that the shoot tips of Attalea seedlings are underground it likely to contribute to their fire-tolerance.[2]
Distribution
Species range across the Neotropics from Mexico in the north to Bolivia, Paraguay, and southern Brazil in the south,[3] from low elevations in coastal Brazil to up to 1,600m (5,200ft) above sea level in the Andes.[6] According to Govaerts and coauthors, three species are found in Mexico, four in Central America, and 62 in South America. Three species are present in the Caribbean—two in Trinidad and Tobago, along the southern edge of the region, and one in Haiti.[26]
Attalea includes both large trees and small, acaulescent palms, which occupy a number of different ecological niches. Dense stands of some of the larger species are conspicuous elements on the landscape, while smaller species are found in both in the forest understorey and in savannas.[3]
Disturbance has been implicated in the formation of vegetation dominated by large Attalea species.[2] In seasonally dry Amazonian forests, the density of large adult A.maripa palms was correlated with canopy openness;[25] the species also dominates savannas formed by repeated forest fires in Trinidad and Tobago.[27]A. speciosa forms pure stands in many parts of Brazil where natural forest vegetation has been cleared.[28] Similarly, stands of A.funifera in Bahia, Brazil (which are cultivated for piassava fibre) are managed using fire—the seedlings survive cutting and burning, and are able to dominate burned forest patches.[29]
The fruit are dispersed by animals; fruit which are not dispersed frequently suffer seed predation by bruchid beetles.[2] Certain species of Attalea have been mentioned as examples of anachronistic species which are adapted for dispersal by now-extinct Pleistocene megafauna.[30][31] On Maracá Island, Roraima, in the Brazilian Amazon, A. maripa fruit were consumed by tapirs, collared peccaries, deer, and primates. Rodents, including agoutis, fed upon the fruit, and as the fruit availability declined, they fed on the seeds.[32] Other dispersers of Attalea fruit include crested caracaras, which consume the fruit and disperse the seeds of A.phalerata in the Brazilian Pantanal.[33]
Uses
Attalea species have a long history of human use. Carbonised Attalea maripa seeds have been found in archaeological sites in Colombia dating back to 9000 BP.[34] Several species remain important sources of edible oil, thatch, edible seeds, and fibre. The leaves of Attalea butyracea and A.maripa are used extensively for thatching. Several species are oil palms, with A.speciosa among the most important economically.[2] Products extracted from A.speciosa were reported to support over 300,000 households in the Brazilian state of Maranhão in 2005,[35] and in 1985 it was estimated to support over 450,000 households throughout the Brazil.[28] Piassava fibres, extracted from the leaf bases of A.funifera, are commercially important,[2] and generated about US$20 million in annual income to Brazilian farmers in 1996.[36]
Related Research Articles
Attalea maripa, commonly called maripa palm is a palm native to tropical South America and Trinidad and Tobago. It grows up 35 m (115 ft) tall and can have leaves or fronds 10–12 m (33–39 ft) long. This plant has a yellow edible fruit which is oblong ovoid and cream. An edible oil can be extracted from the pulp of the fruit and from the kernel of the seed.
Syagrus is a genus of Arecaceae (palms), native to South America, with one species endemic to the Lesser Antilles. The genus is closely related to the Cocos, or coconut genus, and many Syagrus species produce edible seeds similar to the coconut.
Coccothrinax is a genus of palms in the family Arecaceae. There are more than 50 species described in the genus, plus many synonyms and subspecies. A new species was described as recently as 2017. Many Coccothrinax produce thatch. In Spanish-speaking countries, guano is a common name applied to Coccothrinax palms. The species are native throughout the Caribbean, the Bahamas, extreme southern Florida and southeastern Mexico, but most of the species are known only from Cuba.
Iriartea is a genus in the palm family Arecaceae, native to Central and South America. The best-known species – and probably the only one – is Iriartea deltoidea, which is found from Nicaragua, south into Bolivia and a great portion of Western Amazonian basin. It is the most common tree in many forests in which it occurs.
Attalea speciosa, the babassu, babassu palm, babaçu, or cusi, is a palm native to the Amazon Rainforest region in South America. The babassu palm is the predominant species in the Maranhão Babaçu forests of Maranhão and Piauí states.
Desmoncus is a genus of mostly climbing, spiny palms native to the Neotropics. The genus extends from Mexico in the north to Brazil and Bolivia in the south, with two species present in the southeastern Caribbean.
Oenocarpus is a genus of pinnate-leaved palms (Arecaceae) native to Trinidad, southern Central and tropical South America. With nine species and one natural hybrid, the genus is distributed from Costa Rica and Trinidad in the north to Brazil and Bolivia in the south.
Attalea crassispatha is a palm which is endemic to southwest Haiti. The most geographically isolated member of the genus, it is considered a critically endangered species and has been called one of the rarest palms in the Americas.
Chelyocarpus is a genus of small to medium-sized fan palms which are native to northwestern South America. Some are upright trees, while others creep along the ground. Species are used for thatch, to weave hats, stuff pillows and as a source of salt.
Cyphophoenix is a genus of flowering plant in the family Arecaceae. It contains 4 known species, all endemic to New Caledonia. The relationships between Cyphophoenix and some other genera of the tribe Basseliniinae including Physokentia and the New Caledonia endemic Burretiokentia are not clear.
Physokentia is a genus of flowering plant in the palm family, native to certain islands of the western Pacific.
Schippia concolor, the mountain pimento or silver pimeto, is a medium-sized palm species that is native to Belize and Guatemala. Named for its discoverer, Australian botanist William A. Schipp, the species is threatened by habitat loss. It is the sole species in the genus Schippia.
Aphandra is a monotypic genus of flowering plants in the palm family native to the Amazon rainforest vegetation in South America. Its only species is Aphandra natalia, sometimes called mastodon palm or fiber palm, and is used by indigenous peoples in the construction of brooms and other products. This plant is commercially exploited for its edible fruits, and for its leaf sheath and petiole fibers. This fiber is almost equal to the fiber extracted from Attalea funifera and Leopoldinia piassaba, which is called piassava.
Attalea phalerata is a species of palm tree known by the English common name urucuri palm, the Portuguese common name urucurizeiro, and the Spanish common name shapaja. Other common names include motacu and bacuri. It is native to Brazil, Bolivia, Paraguay, and Peru, where it grows along southern and western Amazonia. It is the most common palm tree on the Pantanal.
Clinosperma is a palm tree genus in the family Arecaceae.
Borasseae is a tribe in the palm subfamily Coryphoideae. The tribe ranges from southern Africa and Madagascar north through the Arabian Peninsula to India, Indochina, Indonesia and New Guinea. Several genera are restricted to islands in the Indian Ocean. The two largest genera, Hyphaene and Borassus, are also the most widespread.
Butia stolonifera was an oddly growing palm assigned to the genus Butia found only once in Uruguay in the 19th century, but which now is considered to be uncertain as a valid species.
Attalea funifera, the Bahia piassava, is a species of palm, native to eastern Brazil. It is a major source of piassava fiber, used in brooms and brushes.
Attalea dubia, also known as the Indaiá plant, babassu palm, or bacuaçu palm is a flowering plant in the family Arecaceae, native to the Southern and Southeast Regions of Brazil.
↑ Dransfield, John; Natalie W. Uhl; Conny B. Asmussen; William J. Baker; Madeline M. Harley; Carl E. Lewis (2005). "A New Phylogenetic Classification of the Palm Family, Arecaceae". Kew Bulletin. 60 (4): 559–69. JSTOR25070242.
↑ Moraes R., Mónica; Finn Borchsenius; Ulla Blicher-Mathiesen (1996). "Notes on the Biology and Uses of the Motacú Palm (Attalea phalerata, Arecaceae) from Bolivia". Economic Botany. 50 (4): 423–428. doi:10.1007/BF02866525. JSTOR4255886. S2CID19066490.
↑ Feil, Jan Peter (1996). "Fruit Production of Attalea colenda (Arecaceae) in Coastal Ecuador: An Alternative Oil Resource?". Economic Botany. 50 (3): 300–309. doi:10.1007/BF02907337. JSTOR4255847. S2CID22885187.
↑ Anderson, Anthony B.; William L. Overal; Andrew Henderson (1988). "Pollination Ecology of a Forest-Dominant Palm (Orbignya phalerata Mart.) in Northern Brazil". Biotropica. 20 (3): 192–205. doi:10.2307/2388234. JSTOR2388234.
↑ Uhl, Natalie E.; John Dransfield (1987). Genera Palmarum: a classification of palms based on the work of Harold E. Moore Jr. Lawrence, Kansas: The L. H. Bailey Hortorium and the International Palm Society. pp.503–512. ISBN0-935868-30-5.
↑ Pinheiro, Claudio Urbano B. (2001). "Germination strategies in palms: the case of Schippia concolor in Belize". Brittonia. 53 (4): 519–527. doi:10.1007/BF02809652. S2CID45335410.
↑ Fragoso, Jose M. V. (1997). "Tapir-Generated Seed Shadows: Scale-Dependent Patchiness in the Amazon Rain Forest". Journal of Ecology. 85 (4): 519–29. doi:10.2307/2960574. JSTOR2960574.
↑ Porro, Roberto (2005). "Palms, Pastures, and Swidden Fields: The Grounded Political Ecology of "Agro-Extractive/Shifting-cultivator Peasants" in Maranhão, Brazil". Human Ecology. 33 (1): 17–56. doi:10.1007/s10745-005-1654-2. S2CID153617434.
↑ Voeks, Robert A. (2002). "Reproductive ecology of the piassava palm (Attalea funifera) of Bahia, Brazil". Journal of Tropical Ecology. 18: 121–136. doi:10.1017/s0266467402002079. S2CID84211050.
This page is based on this Wikipedia article Text is available under the CC BY-SA 4.0 license; additional terms may apply. Images, videos and audio are available under their respective licenses.
