The choice of specific epithet to use for our species follows the conclusion reached by D. W. Stevenson (1987).
Controversy has long existed over the classification of Zamia in Florida. Recent researchers, however, have concluded that only one species is present in the flora. The several binomials applied to our Zamia reflect variability in plant vigor, leaf shape, leaflet width, number of marginal teeth and veins per leaflet, and geographic distribution. Forms with wide leaflets---" Zamia umbrosa "---are restricted to coastal hammocks of northeastern Florida and southeastern Georgia and appear to be quite distinct from plants of the remainder of Florida--- Z . integrifolia and " Z . floridana ." Especially robust forms have been described as " Zamia silvicola ." Studies by D. B. Ward (n.d.) indicate that these features have a genetic basis, but formal recognition of these different phases as species does not lead to better understanding of the complex. The variants in Florida may have originated from introductions of divergent forms of Zamia from elsewhere. The starchy stems, after treatment to remove a poisonous principle, were a significant part of aboriginal diets, and the plants were presumably dispersed by aborigines.
Zamia angustifolia Jacquin, a species thought to be restricted to the Bahamas and eastern Cuba, was reported in southern Florida by J. K. Small (1933). No voucher specimens were cited or are known to exist. Small also reported Zamia pumila Linnaeus from Florida, although erroneously.
Zamia integrifolia, also known as coontie palm is a small, tough, woody cycad native to the southeastern United States (in Florida and Georgia), the Bahamas, Cuba, and the Cayman Islands.[1]
Zamia integrifolia produces reddish seed cones with a distinct acuminate tip. The leaves are 20–100 cm long, with 5-30 pairs of leaflets (pinnae). Each leaflet is linear to lanceolate or oblong-obovate, 8–25 cm long and 0.5–2 cm broad, entire or with indistinct teeth at the tip. They are often revolute, with prickly petioles. It is similar in many respects to the closely related Zamia pumila, but that species differs in the more obvious toothing on the leaflets.[3]
This is a low-growing plant, with a trunk that grows to 3–25 cm high, but is often subterranean. Over time, it forms a multi-branched cluster, with a large, tuberous root system, which is actually an extension of the above-ground stems. The leaves can be completely lost during cold periods, with the plant lying dormant in its tuberous root system, allowing this cycad to be relatively cold hardy. The plant can survive up to USDA region 8b (10° to 20°F). The stems and leaves regenerate after the cold period subsides with full foliage.[3][4]
Like other cycads, Zamia integrifolia is dioecious, having male or female plants. The male cones are cylindrical, growing to 5–16 cm long; they are often clustered. The female cones are elongate-ovoid and grow to 5–19 cm long and 4–6 cm in diameter.[3]
Indigenous tribes of Florida like the Seminoles and Tequestas would grind the root and soak it overnight; afterwards, they would rinse it with running water for several hours to remove the rest of the water-soluble toxin cycasin. The resulting paste was then left to ferment before being dried into a powder. The resulting powder could then be used to make a bread-like substance.[5] By the late 1880s, several mills in the Miami area started to produce Florida arrowroot until their demise after the World War 1.[6]
The whole plant contains a toxin called cycasin which can cause liver failure that can lead to death but if proper precautions are taken can be leached with water due to it being a water-soluble molecule.[7] The seeds contain a toxic glycoside which causes headaches, vomiting, stomach pains and diarrhoea if ingested. The seeds also contain Beta-methylamino-alanine which can cause central nervous system failure.[8]
This plant has several common names. Two names, Florida arrowroot and wild sago, refer to the former commercial use of this species as the source of an edible starch. Coontie (or koonti) is derived from the Seminole Native American language conti hateka.
Zamia integrifolia inhabits a variety of habitats with well-drained sands or sandy loam soils. It prefers filtered sunlight to partial shade. Populations are presently limited to Florida (including the Florida Keys) and southeastern Georgia in the United States, western Cuba, the Bahamas (on Andros, Grand Bahama, Great Abaco, Long Island, and New Providence islands), and the Cayman Islands.
Controversy has long existed over the classification of Zamia in Florida; at one extreme all the American populations are included in a broadly defined Zamia pumila species complex,[9] and at the other several species have been recognized under various names (e.g., Z. augustifolia, Z. floridana, Z. silvicola, and Z. umbrosa). The Flora of North America treats all of the American populations as Z. integrifolia, and all West Indian populations as other species. Genetically, the differences between populations cannot be explained by habitat variability. Studies conducted by Ward[10] showed that five different Florida populations of Z. integrifolia with identical cultivation produced distinct leaf morphology, suggesting that there may be too much genetic diversity amongst these Floridian Z. integrifolia, not to mention geographically isolated populations, to consider them a single species.
The plant has critical importance to the Atala butterfly (Eumaeus atala). The butterfly, thought extinct until recently, is dependent for its survival on Z. integrifolia, as well as several other species of Zamia. At the larval stage, the Atala caterpillar exclusively eats the leaves of the coontie. A half dozen caterpillars can completely strip a coontie bare, and a large coontie population is needed to sustain E. atala populations.
Mealybug destroyers (Cryptolaemus montrouzieri), are commonly found on Z. integrifolia. They form a mutualistic relationship by providing the plant protection from pests in exchange for food. They feed on the coonties' natural enemies, scales and mealybugs, thereby reducing the need for pesticides.[11]
Three of the most common pests of Z. integrifolia are Florida red scales (Chrysomphalus aonidum), hemispherical scales (Saissetia coffeae) and longtailed mealybugs (Pseudococcus longispinus). When infested, the plant's growth is stunted, and it becomes covered with blackish mold. Infestations are not limited to one species; several species can be found on the same plant.[12]
Since Z. integrifolia is a cycad, which are the only group of gymnosperms that form nitrogen-fixing associations, it depends on microbes as a source of nitrogen. It forms a symbiotic relationship with nitrogen-fixing cyanobacteria, which live in specialized roots called coralloid roots and are green in color despite not actively photosynthesizing.[13] The filamentous cyanobacteria belonging to the genus Nostoc, which is able to form symbiosis with a wide range of organisms,[14] inhabits the mucilage in the microaerobic and dark intercellular zone in between the inner and outer cortex of coralloid roots. This zone is transversed and connected by elongated Zamia cells.[15] Coralloid roots are just like lateral roots, but highly specialized to contain cyanobacteria.[13]
Zamia species often produce more than one cone close to the tip of the stem or at the terminal of the caudex where it intersects with the cones, also called strobilus, of Z. integrifolia are dioecious. The male strobilus and the female strobilus are found on two separate plants. The cones on the female plant are thick and have red-orange seeds. They also have a velvety texture, and only grow up to 6 inches. On the other hand, the ones on the male plant are narrow and tall, and contain pollen. They can reach a length of 7 inches. Female cones are usually borne singularly, whereas male cones grow in groups or clusters. The growing season of Z. integrifolia is during the spring, and the sex of the plant is undetermined until cones are produced.[11]
The multiple cones of Z. integrifolia may develop through three methods: sympodium, forking of the bundle system, and adventitious buds. The most common form of development is the rapid formation of cone domes on the plant's sympodium, which is its main axis. More cones are present when there is a "branching" of the bundles to the cones. The forking of the bundle system starts near the base of a terminal cone, which remains erect, of the sympodial development in certain branches. The last method is when "adventitious buds appear in the cortical tissue closely connected with the stelar system of the trunk, and these buds continue their development like typical stems".[16]
Z. integrifolia plants are pollinated by two species of weevils, Rhopalotria slossoni and Pharaxonotha floridana. P. floridana pollinates the plants by using the pollen-bearing strobili as food for its larvae, transporting the pollen with it. The plant can regulate the mutualistic interaction by making the seed-bearing strobilis poisonous to these larvae.[17] On the other hand, R. slossoni does not consume the pollen, but rather, takes shelter in male cones where they become dusted with pollen. They then carry over these pollen into the female cones, which becomes pollinated. Although the female cones are not consumed, there have been evidences of healed scars due to punctation in the interior of the cone, which are suspected to be caused by weevils.[18]
Zamia integrifolia, also known as coontie palm is a small, tough, woody cycad native to the southeastern United States (in Florida and Georgia), the Bahamas, Cuba, and the Cayman Islands.
