Cycad Explained

Cycads are seed plants that typically have a stout and woody (ligneous) trunk with a crown of large, hard, stiff, evergreen and (usually) pinnate leaves. The species are dioecious, that is, individual plants of a species are either male or female. Cycads vary in size from having trunks only a few centimeters to several meters tall. They typically grow very slowly[1] and live very long. Because of their superficial resemblance to palms or ferns, they are sometimes mistaken for them, but they are not closely related to either group.Cycads are gymnosperms (naked-seeded), meaning their unfertilized seeds are open to the air to be directly fertilized by pollination, as contrasted with angiosperms, which have enclosed seeds with more complex fertilization arrangements. Cycads have very specialized pollinators, usually a specific species of beetle. Both male and female cycads bear cones (strobili), somewhat similar to conifer cones.

Cycads have been reported to fix nitrogen in association with various cyanobacteria living in the roots (the "coralloid" roots).[2] These photosynthetic bacteria produce a neurotoxin called BMAA that is found in the seeds of cycads. This neurotoxin may enter a human food chain as the cycad seeds may be eaten directly as a source of flour by humans or by wild or feral animals such as bats, and humans may eat these animals. It is hypothesized that this is a source of some neurological diseases in humans.[3] [4] Another defence mechanism against herbivores is the accumulation of toxins in seeds and vegetative tissues; through horizontal gene transfer, cycads have acquired a family of genes (fitD) from a microbial organism, most likely a fungus, which gives them the ability to produce an insecticidal toxin.[5]

Cycads all over the world are in decline, with four species on the brink of extinction and seven species having fewer than 100 plants left in the wild.[6]

Description

Cycads have a cylindrical trunk which usually does not branch. However, some types of cycads, such as Cycas zeylanica, can branch their trunks. The apex of the stem is protected by modified leaves called cataphylls.[7] Leaves grow directly from the trunk, and typically fall when older, leaving a crown of leaves at the top. The leaves grow in a rosette form, with new foliage emerging from the top and center of the crown. The trunk may be buried, so the leaves appear to be emerging from the ground, so the plant appears to be a basal rosette. The leaves are generally large in proportion to the trunk size, and sometimes even larger than the trunk.

The leaves are pinnate (in the form of bird feathers, pinnae), with a central leaf stalk from which parallel "ribs" emerge from each side of the stalk, perpendicular to it. The leaves are typically either compound (the leaf stalk has leaflets emerging from it as "ribs"), or have edges (margins) so deeply cut (incised) so as to appear compound. The Australian genus Bowenia and some Asian species of Cycas, like Cycas multipinnata, Cycas micholitzii and Cycas debaoensis, have leaves that are bipinnate, which means the leaflets each have their own subleaflets, growing in the same form on the leaflet as the leaflets grow on the stalk of the leaf (self-similar geometry).[8] [9]

Confusion with palms

Due to superficial similarities in foliage and plant structure, cycads and palms are often mistaken for each other. They also can occur in similar climates. However, they belong to different phyla and as such are not closely related. The similar structure is the product of convergent evolution.

Beyond those superficial resemblances, there are a number of differences between cycads and palms. For one, both male and female cycads are gymnosperms and bear cones (strobili), while palms are angiosperms and so flower and bear fruit. The mature foliage looks very similar between both groups, but the young emerging leaves of a cycad resemble a fiddlehead fern before they unfold and take their place in the rosette, while the leaves of palms are just small versions of the mature frond. Another difference is in the stem. Both plants leave some scars on the stem below the rosette where there used to be leaves, but the scars of a cycad are helically arranged and small, while the scars of palms are a circle that wraps around the whole stem. The stems of cycads are also in general rougher and shorter than those of palms.[10]

Taxonomy

The two extant families of cycads all belong to the order Cycadales, and are the Cycadaceae and Zamiaceae (including Stangeriaceae). These cycads have changed little since the Jurassic in comparison to some other plant divisions. Five additional families belonging to the Medullosales became extinct by the end of the Paleozoic Era.

Based on genetic studies, cycads are thought to be more closely related to Ginkgo than to other living gymnosperms. Both are thought to have diverged from each other during the early Carboniferous.[11] [12]

Classification of the Cycadophyta to the rank of family.

Fossil genera

The following extinct cycad genera are known:[15]

Fossil record

The oldest probable cycad foliage is known from the latest Carboniferous-Early Permian of South Korea and China, such as Crossozamia. Unambiguous fossils of cycads are known from the Early-Middle Permian onwards.[22] Cycads were generally uncommon during the Permian.[23] The two living cycad families are thought to have split from each other sometime between the Jurassic and Carboniferous.[24] Cycads are thought to have reached their apex of diversity during the Mesozoic.[25] Although the Mesozoic is sometimes called the "Age of Cycads," some other groups of extinct seed plants with similar foliage, such as Bennettitales and Nilssoniales, that are not closely related, may have been more abundant.[26] The oldest records of the modern genus Cycas are from the Paleogene of East Asia.[27] Fossils assignable to Zamiaceae are known from the Cretaceous, with fossils assignable to living genera of the family known from the Cenozoic.

Distribution

See also: List of cycad species by country. The living cycads are found across much of the subtropical and tropical parts of the world, with a few in temperate regions such as in Australia.[28] The greatest diversity occurs in South and Central America. They are also found in Mexico, the Antilles, southeastern United States, Australia, Melanesia, Micronesia, Japan, China, Southeast Asia, Bangladesh, India, Sri Lanka, Madagascar, and southern and tropical Africa, where at least 65 species occur. Some can survive in harsh desert or semi-desert climates (xerophytic),[29] others in wet rain forest conditions,[30] and some in both. Some can grow in sand or even on rock, some in oxygen-poor, swampy, bog-like soils rich in organic material. Some are able to grow in full sun, some in full shade, and some in both. Some are salt tolerant (halophytes).

Species diversity of the extant cycads peaks at 17˚ 15"N and 28˚ 12"S, with a minor peak at the equator. There is therefore not a latitudinal diversity gradient towards the equator but towards the Tropic of Cancer and the Tropic of Capricorn. However, the peak near the northern tropic is largely due to Cycas in Asia and Zamia in the New World, whereas the peak near the southern tropic is due to Cycas again, and also to the diverse genus Encephalartos in southern and central Africa, and Macrozamia in Australia. Thus, the distribution pattern of cycad species with latitude appears to be an artifact of the geographical isolation of the remaining cycad genera and their species, and perhaps because they are partly xerophytic rather than simply tropical.

Cultural significance

Nuts of the Cycas orientis (nyathu) are coveted by the Yolngu in Australia's Arnhem Land as a source of food. They are harvested on their dry season to leach its poison under water overnight before ground into a paste, wrapped under bark and cooked on open fire until done.[31]

In Vanuatu, the cycad is known as namele and is an important symbol of traditional culture. It serves as a powerful taboo sign,[32] and a pair of namele leaves appears on the national flag and coat of arms. Together with the nanggaria plant, another symbol of Vanuatu culture, the namele also gives its name to Nagriamel, an indigenous political movement.

See also

External links

Notes and References

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  2. Rai AN, Soderback E, Bergman B . 2000 . Tansley Review No. 116. Cyanobacterium-Plant Symbioses . The New Phytologist . 147 . 3 . 449–481 . 2588831 . 10.1046/j.1469-8137.2000.00720.x . 33862930 . free .
  3. Holtcamp, W. . 2012 . The emerging science of BMAA: do cyanobacteria contribute to neurodegenerative disease? . Environmental Health Perspectives . 120 . 3 . 10.1289/ehp.120-a110 . 22382274 . 3295368 . a110–a116.
  4. Cox PA, Davis DA, Mash DC, Metcalf JS, Banack SA . 2015 . Dietary exposure to an environmental toxin triggers neurofibrillary tangles and amyloid deposits in the brain . Proceedings of the Royal Society B . 283 . 1823 . 10.1098/rspb.2015.2397 . 20152397 . 26791617 . 4795023.
  5. 10.1038/s41477-022-01129-7 . free . The Cycas genome and the early evolution of seed plants . 2022 . Liu . Yang . Wang . Sibo . Li . Linzhou . Yang . Ting . Dong . Shanshan . Wei . Tong . Wu . Shengdan . Liu . Yongbo . Gong . Yiqing . Feng . Xiuyan . Ma . Jianchao . Chang . Guanxiao . Huang . Jinling . Yang . Yong . Wang . Hongli . Liu . Min . Xu . Yan . Liang . Hongping . Yu . Jin . Cai . Yuqing . Zhang . Zhaowu . Fan . Yannan . Mu . Weixue . Sahu . Sunil Kumar . Liu . Shuchun . Lang . Xiaoan . Yang . Leilei . Li . Na . Habib . Sadaf . Yang . Yongqiong . Nature Plants . 8 . 4 . 389–401 . 35437001 . 9023351 . 1 .
  6. News: Davis . Judi . 2018-06-27 . Meet Durban's famous cycad family . South Coast Herald . 2022-09-11.
  7. 6315973 . 2018 . Marler . T. E. . Krishnapillai . M. V. . Does Plant Size Influence Leaf Elements in an Arborescent Cycad? . Biology . 7 . 4 . 51 . 10.3390/biology7040051 . 30551676 . free .
  8. Book: Rutherford, Catherine . CITES and Cycads: A User's Guide . Royal Botanic Gardens, Kew . et al..
  9. Book: Cycadaceae Family . 9781300654537 . Lariushin . Boris . 19 January 2013 . Lulu.com .
  10. Book: Tudge, Colin . The Tree . Crown Publishers . 2006 . 978-1-4000-5036-9 . New York . 70–72, 139–148 . registration .
  11. Wu . Chung-Shien . Chaw . Shu-Miaw . Huang . Ya-Yi . January 2013 . Chloroplast phylogenomics indicates that Ginkgo biloba is sister to cycads . Genome Biology and Evolution . 5 . 1 . 243–254 . 10.1093/gbe/evt001 . 1759-6653 . 3595029 . 23315384 . en.
  12. Stull . Gregory W. . Qu . Xiao-Jian . Parins-Fukuchi . Caroline . Yang . Ying-Ying . Yang . Jun-Bo . Yang . Zhi-Yun . Hu . Yi . Ma . Hong . Soltis . Pamela S. . Soltis . Douglas E. . Li . De-Zhu . July 19, 2021 . Gene duplications and phylogenomic conflict underlie major pulses of phenotypic evolution in gymnosperms . Nature Plants . 7 . 8 . 1015–1025 . 10.1038/s41477-021-00964-4 . 34282286 . 236141481 . 2055-0278 . en .
  13. Nagalingum . N. S. . Marshall . C. R. . Quental . T. B. . Rai . H. S. . Little . D. P. . Mathews . S. . 2011 . Recent synchronous radiation of a living fossil . Science . 334 . 6057 . 796–799 . 2011Sci...334..796N . 10.1126/science.1209926 . 22021670 . 206535984.
  14. Condamine . Fabien L. . Nagalingum . Nathalie S. . Marshall . Charles R. . Morlon . Hélène . 17 April 2015 . Origin and diversification of living cycads: a cautionary tale on the impact of the branching process prior in Bayesian molecular dating . BMC Evolutionary Biology . 15 . 65 . 10.1186/s12862-015-0347-8 . 25884423. 14815027 . en . free. 4449600 . 2015BMCEE..15...65C .
  15. Web site: PBDB . 2024-03-16 . paleobiodb.org.
  16. Hermsen . Elizabeth J. . Taylor . Edith L. . Taylor . Thomas N. . January 2009 . Morphology and ecology of the Antarcticycas plant . Review of Palaeobotany and Palynology . en . 153 . 1–2 . 108–123 . 10.1016/j.revpalbo.2008.07.005. 2009RPaPa.153..108H .
  17. Xu . Yuanyuan . Popa . Mihai Emilian . Zhang . Tingshan . Lu . Ning . Zeng . Jianli . Zhang . Xiaoqing . Li . Liqin . Wang . Yongdong . 2021-09-01 . Re-appraisal of Anthrophyopsis (Gymnospermae): New material from China and global fossil records . Review of Palaeobotany and Palynology . 292 . 104475 . 10.1016/j.revpalbo.2021.104475 . 2021RPaPa.29204475X . 0034-6667.
  18. Zhang . Jian-Wei . Yao . Jian-Xin . Chen . Jia-Rui . Li . Cheng-Sen . 2010-05-25 . A new species of Leptocycas (Zamiaceae) from the Upper Triassic sediments of Liaoning Province, China . Journal of Systematics and Evolution . en . 48 . 4 . 286–301 . 10.1111/j.1759-6831.2010.00079.x.
  19. Vajda . Vivi . Pucetaite . Milda . McLoughlin . Stephen . Engdahl . Anders . Heimdal . Jimmy . Uvdal . Per . August 2017 . Molecular signatures of fossil leaves provide unexpected new evidence for extinct plant relationships . Nature Ecology & Evolution . en . 1 . 8 . 1093–1099 . 2017NatEE...1.1093V . 10.1038/s41559-017-0224-5 . 2397-334X . 29046567 . 3604369.
  20. Spicer . Robert A. . Herman . Alexey B. . 1996-05-01 . Nilssoniocladus in the Cretaceous Arctic: new species and biological insights . Review of Palaeobotany and Palynology . 92 . 3 . 229–243 . 10.1016/0034-6667(95)00111-5 . 1996RPaPa..92..229S . 0034-6667.
  21. Axsmith . Brian J. . Serbet . Rudolph . Krings . Michael . Taylor . Thomas N. . Taylor . Edith L. . Mamay . Sergius H. . 2003 . The Enigmatic Paleozoic plants Spermopteris and Phasmatocycas reconsidered . American Journal of Botany . en . 90 . 11 . 1585–1595 . 10.3732/ajb.90.11.1585 . 21653333 . 0002-9122.
  22. Spiekermann . Rafael . Jasper . André . Siegloch . Anelise Marta . Guerra-Sommer . Margot . Uhl . Dieter . June 2021 . Not a lycopsid but a cycad-like plant: Iratinia australis gen. nov. et sp. nov. from the Irati Formation, Kungurian of the Paraná Basin, Brazil . Review of Palaeobotany and Palynology . en . 289 . 104415 . 10.1016/j.revpalbo.2021.104415 . 2021RPaPa.28904415S . 233860955.
  23. Gomankov . A. V. . June 2022 . Cycads in the Permian of thе Subangara Region . Paleontological Journal . en . 56 . 3 . 317–326 . 10.1134/S0031030122030066 . 2022PalJ...56..317G . 249627815 . 0031-0301.
  24. Coiro . Mario . Allio . Rémi . Mazet . Nathan . Seyfullah . Leyla J. . Condamine . Fabien L. . 2023-06-11 . Reconciling fossils with phylogenies reveals the origin and macroevolutionary processes explaining the global cycad biodiversity . New Phytologist . 240 . 4 . 1616–1635 . en . 10.1111/nph.19010 . 37302411 . 0028-646X. free . 10953041 .
  25. Coiro . Mario . Seyfullah . Leyla Jean . 2024-03-14 . Disparity of cycad leaves dispels the living fossil metaphor . Communications Biology . en . 7 . 1 . 328 . 10.1038/s42003-024-06024-9 . 2399-3642 . 10940627 . 38485767.
  26. Coiro . Mario . Pott . Christian . December 2017 . Eobowenia gen. nov. from the Early Cretaceous of Patagonia: indication for an early divergence of Bowenia? . BMC Evolutionary Biology . en . 17 . 1 . 97 . 10.1186/s12862-017-0943-x . 1471-2148 . 5383990 . 28388891 . free . 2017BMCEE..17...97C .
  27. Liu . Jian . Lindstrom . Anders J . Marler . Thomas E . Gong . Xun . 2022-01-28 . Not that young: combining plastid phylogenomic, plate tectonic and fossil evidence indicates a Palaeogene diversification of Cycadaceae . Annals of Botany . en . 129 . 2 . 217–230 . 10.1093/aob/mcab118 . free . 0305-7364 . 8796677 . 34520529.
  28. Orchard, A.E. & McCarthy, P.M. (eds.) (1998). Flora of Australia 48: 1-766. Australian Government Publishing Service, Canberra.
  29. National Recovery Plan for the MacDonnell Ranges Cycad Macrozamia macdonnellii . Department of Natural Resources, Environment, The Arts and Sport, Northern Territory . 16 July 2015.
  30. Book: Bermingham, E. . Dick, C.W. . Moritz, C. . 2005 . Tropical Rainforests: Past, Present, and Future . University of Chicago Press . 9780226044682 .
  31. Book: 48. 978-1-921953-31-6. National Museum of Australia Press. Midawarr Harvest: The Art of Mulkun Wirrpanda and John Wolseley . 2017.
  32. Web site: Dan McGarry . Apr 9, 2018 . A Princely Title . Vanuatu Daily Post .