Zamia integrifolia

Zamia integrifolia is a small, tough, woody cycad native to the southeast United States (Florida, Georgia), the Bahamas, Cuba, the Cayman Islands, Hispaniola (Dominican Republic and Haiti), and Puerto Rico.[1] The species is possibly extinct in Puerto Rico and Haiti.

Zamia integrifolia
Leaves of Zamia integrifolia
Scientific classification
Kingdom: Plantae
Clade: Tracheophytes
Division: Cycadophyta
Class: Cycadopsida
Order: Cycadales
Family: Zamiaceae
Genus: Zamia
Species:
Z. integrifolia
Binomial name
Zamia integrifolia
Synonyms[2]

Description

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]

Ediblity and toxicity
Main article: Florida arrowroot

Ediblity
A strainer used by Seminoles to extract an edible starch from coontie root.

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 than left to ferment and then dried into a powder. The resulting powder than could 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]

Toxicity

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 contains 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]

Common names

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.

Ecology

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, southeastern Georgia, central Cuba and the Dominican Republic. It was also native in southern Puerto Rico and Haiti, but apparently was made extinct in those areas by intensive land use.

The Eumaeus atala butterfly is dependent on the coontie for its survival

Controversy has long existed over the classification of Zamia in Florida; at one extreme all the American populations have been included in a broadly defined Zamia pumila[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. 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 Florida Z. integrifolia, not to mention geographically isolated populations, to consider them a single species.

The plant has critical importance to the Eumaeus atala butterfly. The butterfly, thought extinct until recently, is dependent for its survival on the Zamia integrifolia, as well as several other species of Zamia. At the larval stage, the Eumaeus 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 the Eumaeus atala population.

Mealybug destroyers, Cryptolaemus montrouzieri, are commonly found on Z. floridana. 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]

Parasites

Three of the most common pests of Z. floridana 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]

Nitrogen-fixation

Since Z. floridana 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]

Reproduction

The cones, also called strobilus, of Z. floridana 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. floridana is during the spring, and the sex of the plant is undetermined until cones are produced.[11]

Multiple cones

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 aboveground stem. The multiple cones of Z. floridana 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]

Pollination

Z. floridana 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]

References
  1. Stevenson, D.W. (2010). "Zamia integrifolia". IUCN Red List of Threatened Species. 2010: e.T42164A10670852. Retrieved 11 August 2020.
  2. "Zamia integrifolia L.f." Plants of the World Online. Board of Trustees of the Royal Botanic Gardens, Kew. 2017. Retrieved 4 September 2020.
  3. Linnaeus, Carl von f. 1789. Hortus Kewensis 3: 478
  4. Whitelock, L. M. (2002). The Cycads. Portland, OR: Timber Press.
  5. "Coontie (Florida Arrowroot) - Arca del Gusto". Slow Food Foundation. Retrieved 2020-07-06.
  6. Agriculture, Florida Department of; Industry, Consumer Services-Division of Plant (2013-01-23). "Do You Know Coontie? Florida's Native Indians and Settlers Did". Florida Department of Agriculture and Consumer Services - Division of Plant Industry. Retrieved 2020-07-06.
  7. "Coontie Palm Poisoning in Dogs - Symptoms, Causes, Diagnosis, Treatment, Recovery, Management, Cost". wagwalking.com. Retrieved 2020-07-06.
  8. "Zamia spp Zamia cycads. Pine cone cycad PFAF Plant Database". pfaf.org. Retrieved 2020-07-06.
  9. Eckenwalder, J. E. 1980. Taxonomy of the West Indian cycads. J. Arnold Arboretum 61: 701-722.
  10. Ward, D.B. (1978). Rare and Endangered Biota of Florida 5: 122-124.
  11. Culbert, Daniel F. (2016-09-28). "Florida Coonties and Atala Butterflies". edis.ifas.ufl.edu. Retrieved 2017-11-27.
  12. "Lawn, Garden, and Landscape Resources - Lee County Extension". lee.ifas.ufl.edu. Retrieved 2017-11-27.
  13. Yamada, Shuntaro; Ohkubo, Satoshi; Miyashita, Hideaki; Setoguchi, Hiroaki (2012-09-01). "Genetic diversity of symbiotic cyanobacteria in Cycas revoluta (Cycadaceae)". FEMS Microbiology Ecology. 81 (3): 696–706. doi:10.1111/j.1574-6941.2012.01403.x. ISSN 0168-6496. PMID 22537413.
  14. Gehringer, Michelle M.; Pengelly, Jasper J. L.; Cuddy, William S.; Fieker, Claus; Forster, Paul I.; Neilan, Brett A. (2010-05-11). "Host Selection of Symbiotic Cyanobacteria in 31 Species of the Australian Cycad Genus: Macrozamia (Zamiaceae)". Molecular Plant-Microbe Interactions. 23 (6): 811–822. doi:10.1094/mpmi-23-6-0811. ISSN 0894-0282. PMID 20459320.
  15. Lindblad, P.; Bergman, B.; Hofsten, A. V.; Hallbom, L.; Nylund, J. E. (1985). "The Cyanobacterium-Zamia Symbiosis: An Ultrastructural Study". The New Phytologist. 101 (4): 707–716. doi:10.1111/j.1469-8137.1985.tb02876.x. JSTOR 2432904.
  16. Smith, Frances Grace (1929-10-01). "Multiple Cones in Zamia Floridana". Botanical Gazette. 88 (2): 204–217. doi:10.1086/333990. ISSN 0006-8071. S2CID 85360270.
  17. "UNF - UNF Landscape - Zamia floridana syn Z integrifolia or Z pumila - Coontie". www.unf.edu. Retrieved 2017-11-26.
  18. "Beetle pollination of two species of Zamia: Evolutionary and ecological considerations (PDF Download Available)". ResearchGate. Retrieved 2017-11-26.
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