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Classification System: APG IV

Superregnum: Eukaryota
Regnum: Plantae
Cladus: Angiosperms
Cladus: Monocots
Cladus: Commelinids
Ordo: Arecales

Familia: Arecaceae
Subfamilia: Coryphoideae
Tribus: Sabaleae
Genus: Sabal
Species: S. bermudana – S. causiarum – S. domingensis – S. etonia – S. gretherae – S. maritima – S. mauritiiformis – S. mexicana – S. minor – S. palmetto – S. pumos – S. rosei – S. uresana – S. yapa

Nothopsecies: S. × brazoriensis

Paleospecies: †S. bracknellense – †S. jenkinsii
Name

Sabal Adans., Fam. Pl. 2: 495 (1763)

Type species: Sabal minor (Jacq.) Pers., Syn. Pl. 1: 399 (1805) Designated as synonym Sabal adansonii Guerns., Bull. Sci. Soc. Philom. Paris 3: 206 (1803), nom. illeg. superfl.

Synonyms

Heterotypic
Inodes O.F.Cook, Bull. Torrey Bot. Club 28: 529 (1901)

References

Adanson (1763) Familles des Plantes, 2: 495, 599.
Govaerts, R. et al. 2015. Sabal in World Checklist of Selected Plant Families. The Board of Trustees of the Royal Botanic Gardens, Kew. Published online. Accessed: 2015 Nov. 15. Reference page.
International Plant Names Index. 2015. Sabal. Published online. Accessed: Nov. 15 2015.
Manchester, Steven. R. (1994) Fruits and seeds of the Middle Eocene Nut Beds Flora, Clarno Formation, Oregon Palaeontographica Americana 58: 1–205.
Tropicos.org 2015. Sabal. Missouri Botanical Garden. Published online. Accessed: 15 Nov. 2015.

Vernacular names
English: Scrub palmetto
magyar: Szabalpálma

Sabal is a genus of palms (or fan-palms) endemic to the New World. Currently, there are 17 recognized species of Sabal, including one hybrid species.[4] The species are native to the subtropical and tropical regions of the Americas, from the Gulf Coast/South Atlantic states in the Southeastern United States, south through the Caribbean, Mexico, and Central America to Colombia and Venezuela. Members of this genus are typically identified by the leaves which originate from a bare, unarmed petiole in a fan-like structure. All members of this genus have a costa (or midrib) that extends into the leaf blade. This midrib can vary in length; and it is due to this variation that leaf blades of certain species of Sabal are strongly curved or strongly costapalmate (as in Sabal palmetto and Sabal etonia) or weakly curved (almost flattened), weakly costapalmate, (as in Sabal minor). Like many other palms, the fruit of Sabal are drupe, that typically change from green to black when mature.

Species

Image Scientific name Common name Distribution
Sabal antillensis M.P.Griff. Antillean palmetto Curaçao[4][5]
Sabal bermudana 3zz.jpg Sabal bermudana L.H.Bailey Bermuda palmetto Bermuda
Sabal causiarum2 edit.jpg Sabal causiarum (O.F. Cook) Becc. Puerto Rico palmetto Puerto Rico, British Virgin Islands, and Hispaniola (Haiti and the Dominican Republic)
Sabal domingensis 5zz.jpg Sabal domingensis Becc. Hispaniola palmetto Cuba and Hispaniola (the Dominican Republic and Haiti)
Sabal etonia 3zz.jpg Sabal etonia Swingle ex Nash Scrub palmetto Peninsular Florida, United States
Sabal gretherieae0.jpg Sabal gretheriae H.J.Quero.R. Yucatán palmetto Quintana Roo, Mexico
Sabal lougheediana M.P.Griff. Bonaire palmetto Bonaire[5]
Sabal-maritima.jpg Sabal maritima (Kunth) Burret Jamaica palmetto Jamaica and Cuba
Sabal mauritiiformis 12zz.jpg Sabal mauritiiformis (H.Karst.) Griseb. & H.Wendl. Savannah palm or palma de vaca Southern Mexico to northern Colombia, Venezuela, and Trinidad
Sabal mexicana 1.jpg Sabal mexicana Mart. Mexican palmetto Southern Texas south through Mexico to Nicaragua
Gardenology.org-IMG 2114 hunt0903.jpg Sabal miamiensis Miami palmetto Southern Florida
Gardenology.org-IMG 0529 hunt07mar.jpg Sabal minor (Jacq.) Pers. Dwarf palmetto northeastern Mexico and Southeastern United States, from Florida north to North Carolina, west to Texas
Spalmetto2.JPG Sabal palmetto (Walter) Lodd. ex Schult. & Schult.f. Cabbage palmetto Cuba, the Bahamas, Turks and Caicos Islands, and the Southeastern United States, from Florida north to North Carolina
Sabal pumos (Scott Zona) 001.jpg Sabal pumos (Kunth) Burret Royal palmetto Guerrero, Michoacán, and Puebla, Mexico
Sabal rosei 2.jpg Sabal rosei (O.F.Cook) Becc. Rosei palmetto coast of northwestern Mexico
Sabal uresana Tucson Arizona May 2012.JPG Sabal uresana Trel. Sonoran palmetto Chihuahua and Sonora, Mexico
Sabal yapa 4zz.jpg Sabal yapa C.Wright ex Becc. Yucatán Peninsula in Mexico, Belize, Cuba, and Guatemala[6][7]

Sabal × brazoriensis D.H.Goldman, Lockett & Read (S. minor × S. palmetto) - Texas[8]

Fossil of S. major
Prehistoric taxa

Extinct species within this genus include:[9]

Sabal bigbendense Manchester et al. 2010†
Sabal bracknellense (Chandler) Mai†[10]
Sabal grayana Brown 1962†
Sabal imperialis Brown 1962†
Sabal jenkinsii† (Reid & Chandler) Manchester†[10]

Formerly placed here

Serenoa repens (W.Bartram) Small (as S. serrulata (Michx.) Nutt. ex Schult. & Schult.f.)[7]

Fossil record

These plants lived from the late Cretaceous to the Quaternary period (from 66 million to 12 thousand years ago). Fossils have been found in United States, Italy, Switzerland, Germany, Japan, the United Kingdom, and France.[9] Leaf fossils of †Sabal lamanonis have been recovered from rhyodacite tuff of Lower Miocene age in Southern Slovakia near the town of Lučenec.[11]27 million years old †Sabal lamanonis and †Sabal raphipholia leaf fossils in volcanic rocks have been described from the Evros region in Western Thrace, Greece,itzerland.html">Switzerland.[12]
Phylogenetic work in Sabal (1990s – present)

The name Sabal was first applied to members of the group by Michel Adanson in the 18th century.[13] Previous names that this genus was associated with include Corypha, Chamaerops, Rhapis.[14][13] This section highlights important phylogenetic work done within the genus Sabal.

In 1990, Scott Zona outlined key morphological and anatomical characters that he used to analyze species relationships of Sabal. Through this analysis of characters, Zona produced a cladogram that portrays evolutionary relationships amongst 15 species of Sabal.[14] Based on the distribution of species within his cladogram, Zona recognized four distinct clades.[14] The clades within his study include (Clade 1) Sabal minor; (Clade 2) Sabal bermudana, Sabal palmetto, Sabal miamiensis, and Sabal etonia; (Clade 3) Sabal maritima, Sabal domingensis, Sabal causiarum, Sabal maurittiformis, Sabal yapa, Sabal mexicana, and Sabal guatemalensis; (Clade 4) Sabal uresana, Sabal rosei, and Sabal pumos.[14] These clades associate closely with geographic distributions.[14] All of the species within Clade 3 occur in the Greater Antilles and southern Mexico, where species that occur in the Greater Antilles are more closely related to each other than those that occur in southern Mexico.[14] Although Clade 4 also occurs in Mexico, these species occur on the west coast where they are geographically separated from the Mexican species within the southern part of the country.[14] The remaining two clades, Clade 1 and Clade 2 predominantly occur in the southeastern United States although S. palmetto and S. minor are also known from Cuba and the Bahamas (S. palmetto) and northern Mexico (S. minor).[14] Sabal bermudana is only known from the Bermuda Islands.[14]

In 2016 Heyduk, Trapnell, Barrett, and Leebens-Mack conducted a new study on Sabal that analyzed molecular (e.g. nuclear, plastid) data from 15 species of the group.[15] This study incorporated plastid and nuclear sequence data that together were used to estimate the relatedness between the species of Sabal.[15] The results of the study show species relationships to be different from the distribution of Zona's cladogram.[14][15] Within the framework of this study, a major difference between the results of Zona and this study is the placement of "Clade 4" (Sabal uresana, Sabal rosei, and Sabal pumos) which split and integrate these species throughout the phylogeny of Sabal.[14][15] The largest of the clades identified by Zona, "Clade 3" is disrupted significantly as it is split into multiple clades.[14][15] Although Sabal causiarum and S. domingensis retain their relationship as sister species, they are included in a clade that also includes S. maritima and S. rosei.[14][15] Despite these disruptions in placement between these two studies, the overall integrity of "Clade 1" and "Clade 2" is in congruence with the clades established from the molecular data.[15][14]
Pollinators and parasitoids

Sabal species are used as food sources by several species of birds including Mimus polyglottos, Turdus migratorius, Dendroica coronata, Corvus ossifragus, and Drycopus pileatus, Caryobruchus,[16] and various species of hymenoptera. Bears (Ursus americanus) and racoons are also known to feed on fruit of various species of Sabal. Sabal palmetto is recorded to have its own lichen, Arthonia rubrocincta,[17] that only occurs on the leaf bases of the Cabbage Palm (Sabal palmetto). In Europe, the introduced Lepidopteran species Paysandisia archon has become a prominent pest whose larvae are known to feed on some of the cultivated species of Sabal.
Uses

Arborescent species are often transplanted from natural stands into urban landscapes and are rarely grown in nurseries due to slow growth. Several species are cultivated as ornamental plants and because several species are relatively cold-hardy, can be grown farther north than most other palms. The central bud of Sabal palmetto is edible and, when cooked, is known as 'swamp cabbage'. Mature fronds are used as thatch, to make straw hats, and for weaving mats.
Symbolic use

A silhouette of a palmetto (S. palmetto) appears on the official flag of South Carolina.[18]

Two images of S. palmetto appear on the Florida state seal.

Sabal palmetto is the state tree of both Florida and South Carolina.
References

Michel Adanson (1763). Familles des plantes. 2 (in French). chez Vincent. pp. 495, 599.
"Sabal Adans". TROPICOS. Missouri Botanical Garden. Retrieved 2009-10-16.
"Sabal Adans". Germplasm Resources Information Network. United States Department of Agriculture. 2004-10-15. Archived from the original on 2009-08-26. Retrieved 2010-04-12.
Griffith, M. Patrick; De Freitas, John; Barros, Michelle; Noblick, Larry R. (2017). "Sabal antillensis (Arecaceae): a new palmetto species from the Leeward Antilles". Phytotaxa. 303: 56–64. doi:10.11646/phytotaxa.303.1.4.
Griffith, M. Patrick; Coolen, Quirijn; Barros, Michelle; Noblick, Larry R. (2019). "Sabal lougheediana (Arecaceae), a critically endangered, endemic palm species from Bonaire". Phytotaxa. 420: 095–102. doi:10.11646/phytotaxa.420.2.1.
"Subordinate taxa of Sabal Adans". TROPICOS. Missouri Botanical Garden. Retrieved 2009-10-16.
"GRIN Species Records of Sabal". Germplasm Resources Information Network. United States Department of Agriculture. Archived from the original on 2015-09-24. Retrieved 2010-07-07.
GOLDMAN, DOUGLAS H.; KLOOSTER, MATTHEW R.; GRIFFITH, M. PATRICK; FAY, MICHAEL F.; CHASE, MARK W. (2011-08-19). "A preliminary evaluation of the ancestry of a putative Sabal hybrid (Arecaceae: Coryphoideae), and the description of a new nothospecies, Sabal × brazoriensis". Phytotaxa. 27 (1): 8. doi:10.11646/phytotaxa.27.1.2. ISSN 1179-3163.
Paleobiology Database
Manchester, Steven R. (1994). "Fruits and seeds of the Middle Eocene Nut Beds Flora, Clarno Formation, Oregon". Palaeontographica Americana. 58: 1–205.
Vojtko, Rastislav (2016-10-21). "Miocénna flóra z lokalít Kalonda a Mučín" [Miocene flora from the localities Kalonda and Mučín]. Acta Geologica Slovaca (in Slovak). 1 (1): 65–70. ISSN 1338-0044. Retrieved 2019-07-08.
Review of the Cenozoic floras and vegetation of Greece by Dimitrios Velitzelos, Johannes M. Bouchal and Thomas Denk - Review of Palaeobotany and Palynology, Volume 204, May 2014, Pages 56-117
Ramp, Paul F.; Thien, Leonard B. (1995). "A Taxonomic History and Reexamination of Sabal minor in the Mississippi Valley". Principes. 39 (2): 77–83.
Zona, Scott (1990). "A Monograph of Sabal (Arecaceae: Coryphoideae)". Aliso. 12 (4): 583–666. doi:10.5642/aliso.19901204.02.
Heyduk, Karolina; Trapnell, Dorset W.; Barrett, Craig F.; Leebens-Mack, Jim (2015-05-13). "Phylogenomic analyses of species relationships in the genus Sabal (Arecaceae) using targeted sequence capture". Biological Journal of the Linnean Society. 117 (1): 106–120. doi:10.1111/bij.12551. ISSN 0024-4066.
i Monteys, Víctor Sarto; Aguilar, Lluís; Saiz‐Ardanaz, Marienza; Ventura, Daniel; Martí, Mercè (June 2005). "Comparative morphology of the egg of the castniid palm borer, Paysandisia archon (Burmeister, 1880) (Lepidoptera: Castniidae)". Systematics and Biodiversity. 3 (2): 179–201. doi:10.1017/S1477200005001635. ISSN 1477-2000. S2CID 85748924.
Grube, Martin; Lucking, Robert; Umana-Tenorio, Loengrin (September 2004). "A New Isidiate Species of Arthonia (Ascomycota: Arthoniaceae) from Costa Rica". Mycologia. 96 (5): 1159. doi:10.2307/3762099. ISSN 0027-5514. JSTOR 3762099. PMID 21148936.
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