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Zygnematophyceae

Zygnematophyceae (or Conjugatophyceae) is a class of green algae in the paraphylum streptophyte algae, also referred to as Charophyta,[2] consisting of more than 4000 described species.[3] The Zygnematophyceae are the sister clade of the Embryophyta (land plants).[4][5][6]

Zygnematophyceae
Conjugation in Spirogyra.
Scientific classification
(unranked): Viridiplantae
(unranked): Charophyta
Class: Zygnematophyceae
Round, 1971
Subclasses
  • Subclass Zygnematophycidae
  • Subclass Spirogloeophycidae
    • Order Spirogloeales
Synonyms[1]
  • Akontae Blackman & Tansley, 1902
  • Conjugatophyceae Engler, 1892
  • 'Conjugatae' Engler, 1892
  • Gamophyceae
  • Saccodermae Pascher ex Kossinskaja, 1952
  • Zygnemaphyceae Round 1971
  • Zygophyceae Widder, 1960

Common members of the Zygnematophyceae include the filamentous algae Spirogyra and Mougeotia, as well as desmids, which are microscopic algae characterized by symmetrical and elaborately ornate cells.[7]

Morphology edit

The body plan of Zygnematophyceae is simple, and the group appears to have gone through a secondary loss of morphological complexity.[8] The most basal members are unicellular, but filamentous species have evolved at least five times,[9] and a few species form colonies.[7] Each cell contains a single nucleus.[7]

The chloroplasts of the Zygnematophyceae are large, typically axile but sometimes parietally located, and contain one or several pyrenoids. One or several chloroplasts may be present in a single cell. The shape of the chloroplast may be star-shaped (in Zygnema), ribbon-shaped (in Spirogyra), or elaborately lobed and dissected. In some taxa, particularly Mougeotia, the chloroplast is able to move in response to different light conditions.[7]

In the Zygnematophyceae, cell walls are composed of three layers: one outer layer consisting of mucus, a primary wall consisting of microfibrils, and an innermost layer of cellulosic microfibrils. Some species shed their primary wall and retain only the innermost layer. The cell wall may be variously decorated with striations, granules, or spines. In the Desmidiales, there are pores in the cell wall which allow the cell to extrude a layer of mucilage for protection.[7]

Several Zygnematophyceae contain genes involved in protection from desiccation that appear to have been derived by horizontal gene transfer from bacteria; the genes are found in plants, Zygnematophyceae, and bacteria, but no other organisms. The genes may have helped to enable plants to make the transition to life on land.[10][11]

A new subclass called Spirogloeophycidae, represented by the species Spirogloea muscicola, was established after the unicellular subaerial algae, resembling a "gelatinous blob", was rediscovered on a rock close to a river bank near Cologne in 2006, after first being discovered in France in 1845.[12]

Reproduction edit

The Zygnematophyceae are able to reproduce both asexually and sexually. Asexual reproduction takes place via fragmentation, cell division, akinete formation, or parthenospores.[7]

Sexual reproduction in the Zygnematophyceae takes place through a process called conjugation.[13] Unusually, the gametes lack flagella,[7] and they also lack centrioles which suggest that flagella were not secondarily lost. This lack of flagella sets the Zygnematophyceae apart from nearly all groups of algae, except for red algae and cyanobacteria (also known as blue-green algae, if they are classified as such).[1] The gametes are scarcely differentiated from vegetative cells.[7]

In conjugation, cells or filaments of opposite sex line up, and tubes form between corresponding cells. The male cells then become amoeboid and crawl across the female, or sometimes both cells crawl into the connecting tube. The cells then meet and fuse to form a zygote, which later undergoes meiosis to produce new cells or filaments. As in land plants, only the female passes its chloroplasts on to the offspring.[citation needed]

Taxonomy edit

The Zygnematophyceae is monophyletic. Traditionally, it has been known to contain two orders, the Zygnematales and Desmidiales.[7] However, the Zygnematales were found to be paraphyletic with respect to the Desmidiales, and so it was split up. As of 2023, five orders and two subclasses are recognized: the Spirogloeales in Spirogloeophycidae, and the Serritaeniales, the Zygnematales, the Spirogyrales, and the Desmidiales in Zygnematophycidae.[9]

Class Zygnematophyceae[14]

  • Subclass Spirogloeophycidae Melkonian, Gontcharov & Marin 2019[11]
    • Order Spirogloeales Melkonian, Gontcharov & Marin 2019
      • Family Spirogloeaceae Melkonian, Gontcharov & Marin 2019
  • Subclass Zygnematophycidae Melkonian, Gontcharov & Marin 2019
    • Order Serritaeniales Hess & de Vries 2022
      • Family Serritaeniaceae Hess & de Vries 2022
    • Order Zygnematales Borge & Pascher 1931
    • Order Spirogyrales Hess & de Vries 2022
      • Family Spirogyraceae Palla 1894
    • Order Desmidiales Krieger 1933

Phylogeny edit

A phylogeny of the families of Zygnematophyceae is presented below:[15][11]

Zygnematophyceae
Spirogloeophycidae
Spirogloeales

Spirogloeaceae

Zygnematophycidae
Serritaeniales

Serritaeniaceae

Habitat edit

Members of the Zygnematophyceae are common in nearly all freshwater habitats, particularly filamentous genera such as Spirogyra and Mougeotia. Some Spirogyra species can tolerate disturbed habitats. On the other hand, desmids (the Desmidiales) often prefer bogs, peatlands, and lakes.[16]

Fossil record edit

Vegetative cells of the Zygnematophyceae are fragile and usually not preserved, but the zygospores are resistant to decay and can become fossilized. The Zygnematophyceae have been recorded from at least the middle Devonian period, and before the Carboniferous period, all the major groups had diverged. Fossils of zygospores are indicators of warming spring conditions and shallow, stagnant mesotrophic habitats.[7]

Genomes edit

The first genomes published for Zygnematophyceae were Mesotaenium endlicherianum and Spirogloea muscicola.[11] Since then, genomes have been published on Penium margaritaceum,[17] Zygnema spp.,[18] and the Closterium peracerosum–strigosum–littorale complex.[19] Furthermore, the gene models of Mesotaenium endlicherianum have been updated.[20]

References edit

  1. ^ a b Guiry, Michael D. (15 March 2013). "Taxonomy and nomenclature of the Conjugatophyceae (= Zygnematophyceae)". Algae. 28 (1): 1–29. doi:10.4490/algae.2013.28.1.001. hdl:10379/11755.
  2. ^ Gontcharov, A. A.; Marin, B; Melkonian, M (5 December 2003). "Are Combined Analyses Better Than Single Gene Phylogenies? A Case Study Using SSU rDNA and rbcL Sequence Comparisons in the Zygnematophyceae (Streptophyta)". Molecular Biology and Evolution. 21 (3): 612–624. doi:10.1093/molbev/msh052. PMID 14739253.
  3. ^ Pichrtová, Martina; Holzinger, Andreas; Kulichová, Jana; Ryšánek, David; Šoljaková, Tereza; Trumhová, Kateřina; Nemcova, Yvonne (8 October 2018). "Molecular and morphological diversity of Zygnema and Zygnemopsis (Zygnematophyceae, Streptophyta) from Svalbard (High Arctic)". European Journal of Phycology. 53 (4): 492–508. doi:10.1080/09670262.2018.1476920. PMC 6235541. PMID 30487730.
  4. ^ Wickett, Norman J.; Mirarab, Siavash; Nguyen, Nam; Warnow, Tandy; Carpenter, Eric; Matasci, Naim; Ayyampalayam, Saravanaraj; Barker, Michael S.; Burleigh, J. Gordon; Gitzendanner, Matthew A.; Ruhfel, Brad R.; Wafula, Eric; Der, Joshua P.; Graham, Sean W.; Mathews, Sarah; Melkonian, Michael; Soltis, Douglas E.; Soltis, Pamela S.; Miles, Nicholas W.; Rothfels, Carl J.; Pokorny, Lisa; Shaw, A. Jonathan; DeGironimo, Lisa; Stevenson, Dennis W.; Surek, Barbara; Villarreal, Juan Carlos; Roure, Béatrice; Philippe, Hervé; dePamphilis, Claude W.; Chen, Tao; Deyholos, Michael K.; Baucom, Regina S.; Kutchan, Toni M.; Augustin, Megan M.; Wang, Jun; Zhang, Yong; Tian, Zhijian; Yan, Zhixiang; Wu, Xiaolei; Sun, Xiao; Wong, Gane Ka-Shu; Leebens-Mack, James (11 November 2014). "Phylotranscriptomic analysis of the origin and early diversification of land plants". Proceedings of the National Academy of Sciences. 111 (45): E4859–E4868. Bibcode:2014PNAS..111E4859W. doi:10.1073/pnas.1323926111. PMC 4234587. PMID 25355905.
  5. ^ de Vries, Jan; Stanton, Amanda; Archibald, John M.; Gould, Sven B. (June 2016). "Streptophyte Terrestrialization in Light of Plastid Evolution". Trends in Plant Science. 21 (6): 467–476. doi:10.1016/j.tplants.2016.01.021. PMID 26895731.
  6. ^ Gitzendanner, Matthew A.; Soltis, Pamela S.; Wong, Gane K.-S.; Ruhfel, Brad R.; Soltis, Douglas E. (March 2018). "Plastid phylogenomic analysis of green plants: A billion years of evolutionary history". American Journal of Botany. 105 (3): 291–301. doi:10.1002/ajb2.1048. PMID 29603143.
  7. ^ a b c d e f g h i j Hall, John D.; McCourt, Richard M. (2017). "Zygnematophyta". Handbook of the Protists. pp. 135–163. doi:10.1007/978-3-319-28149-0_41. ISBN 978-3-319-28149-0.
  8. ^ Nishiyama, Tomoaki; Sakayama, Hidetoshi; de Vries, Jan; Buschmann, Henrik; Saint-Marcoux, Denis; Ullrich, Kristian K.; Haas, Fabian B.; Vanderstraeten, Lisa; Becker, Dirk; Lang, Daniel; Vosolsobě, Stanislav; Rombauts, Stephane; Wilhelmsson, Per K.I.; Janitza, Philipp; Kern, Ramona; Heyl, Alexander; Rümpler, Florian; Villalobos, Luz Irina A. Calderón; Clay, John M.; Skokan, Roman; Toyoda, Atsushi; Suzuki, Yutaka; Kagoshima, Hiroshi; Schijlen, Elio; Tajeshwar, Navindra; Catarino, Bruno; Hetherington, Alexander J.; Saltykova, Assia; Bonnot, Clemence; Breuninger, Holger; Symeonidi, Aikaterini; Radhakrishnan, Guru V.; Van Nieuwerburgh, Filip; Deforce, Dieter; Chang, Caren; Karol, Kenneth G.; Hedrich, Rainer; Ulvskov, Peter; Glöckner, Gernot; Delwiche, Charles F.; Petrášek, Jan; Van de Peer, Yves; Friml, Jiri; Beilby, Mary; Dolan, Liam; Kohara, Yuji; Sugano, Sumio; Fujiyama, Asao; Delaux, Pierre-Marc; Quint, Marcel; Theißen, Günter; Hagemann, Martin; Harholt, Jesper; Dunand, Christophe; Zachgo, Sabine; Langdale, Jane; Maumus, Florian; Van Der Straeten, Dominique; Gould, Sven B.; Rensing, Stefan A. (July 2018). "The Chara Genome: Secondary Complexity and Implications for Plant Terrestrialization". Cell. 174 (2): 448–464.e24. doi:10.1016/j.cell.2018.06.033. PMID 30007417. S2CID 206569169.
  9. ^ a b Hess, Sebastian; Williams, Shelby K.; Busch, Anna; Irisarri, Iker; Delwiche, Charles F.; Vries, Sophie de; Darienko, Tatyana; Roger, Andrew J.; Archibald, John M.; Buschmann, Henrik; Schwartzenberg, Klaus von; Vries, Jan de (2022-09-01). "A phylogenomically informed five-order system for the closest relatives of land plants". Current Biology. 32 (20): 4473–4482.e7. doi:10.1016/j.cub.2022.08.022. ISSN 0960-9822. PMC 9632326. PMID 36055238.
  10. ^ Zimmer, Carl (14 November 2019). "How Did Plants Conquer Land? These Humble Algae Hold Clues". The New York Times.
  11. ^ a b c d Cheng, Shifeng; Xian, Wenfei; Fu, Yuan; Marin, Birger; Keller, Jean; Wu, Tian; Sun, Wenjing; Li, Xiuli; Xu, Yan; Zhang, Yu; Wittek, Sebastian; Reder, Tanja; Günther, Gerd; Gontcharov, Andrey; Wang, Sibo; Li, Linzhou; Liu, Xin; Wang, Jian; Yang, Huanming; Xu, Xun; Delaux, Pierre-Marc; Melkonian, Barbara; Wong, Gane Ka-Shu; Melkonian, Michael (2019). "Genomes of Subaerial Zygnematophyceae Provide Insights into Land Plant Evolution". Cell. 179 (5): 1057–1067.e14. doi:10.1016/j.cell.2019.10.019. PMID 31730849.
  12. ^ Ancient plants learned to survive on land by stealing other species' DNA
  13. ^ Kapraun, D. F. (30 November 2006). "Nuclear DNA Content Estimates in Green Algal Lineages: Chlorophyta and Streptophyta". Annals of Botany. 99 (4): 677–701. doi:10.1093/aob/mcl294. PMC 2802934. PMID 17272304.
  14. ^ Guiry, M.D.; Guiry, G.M. "Zygnematophyceae". AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. Retrieved 2023-04-30.
  15. ^ Stancheva, Rosalina; Hall, John D.; Herburger, Klaus; Lewis, Louise A.; Mccourt, Richard M.; Sheath, Robert; Holzinger, Andreas (July 2014). "Phylogenetic position of Zygogonium ericetorum (Zygnematophyceae, Charophyta) from a high alpine habitat and ultrastructural characterization of unusual aplanospores". Journal of Phycology. 50 (5): 790–803. doi:10.1111/jpy.12229. PMC 4370237. PMID 25810560.
  16. ^ Hall, John D.; McCourt, Richard M. (2014). "Chapter 9. Conjugating Green Algae Including Desmids". In Wehr, John D.; Sheath, Robert G.; Kociolek, J. Patrick (eds.). Freshwater Algae of North America: Ecology and Classification (2 ed.). Elsevier Inc. ISBN 978-0-12-385876-4.
  17. ^ Jiao, Chen; Sørensen, Iben; Sun, Xuepeng; Sun, Honghe; Behar, Hila; Alseekh, Saleh; Philippe, Glenn; Palacio Lopez, Kattia; Sun, Li; Reed, Reagan; Jeon, Susan; Kiyonami, Reiko; Zhang, Sheng; Fernie, Alisdair R.; Brumer, Harry (May 2020). "The Penium margaritaceum Genome: Hallmarks of the Origins of Land Plants". Cell. 181 (5): 1097–1111.e12. doi:10.1016/j.cell.2020.04.019. PMID 32442406. S2CID 218763002.
  18. ^ Feng, Xuehuan; Zheng, Jinfang; Irisarri, Iker; Yu, Huihui; Zheng, Bo; Ali, Zahin; De Vries, Sophie; Keller, Jean; Fürst-Jansen, Janine M.R. (2023-02-01). Chromosome-level genomes of multicellular algal sisters to land plants illuminate signaling network evolution (Report). Evolutionary Biology. doi:10.1101/2023.01.31.526407. PMC 9915684. PMID 36778228.
  19. ^ Sekimoto, Hiroyuki; Komiya, Ayumi; Tsuyuki, Natsumi; Kawai, Junko; Kanda, Naho; Ootsuki, Ryo; Suzuki, Yutaka; Toyoda, Atsushi; Fujiyama, Asao; Kasahara, Masahiro; Abe, Jun; Tsuchikane, Yuki; Nishiyama, Tomoaki (March 2023). "A divergent RWP‐RK transcription factor determines mating type in heterothallic Closterium". New Phytologist. 237 (5): 1636–1651. doi:10.1111/nph.18662. ISSN 0028-646X. PMID 36533897. S2CID 254918679.
  20. ^ Dadras, Armin; Fürst-Jansen, Janine M. R.; Darienko, Tatyana; Krone, Denis; Scholz, Patricia; Sun, Siqi; Herrfurth, Cornelia; Rieseberg, Tim P.; Irisarri, Iker; Steinkamp, Rasmus; Hansen, Maike; Buschmann, Henrik; Valerius, Oliver; Braus, Gerhard H.; Hoecker, Ute (2023-08-28). "Environmental gradients reveal stress hubs pre-dating plant terrestrialization". Nature Plants. 9 (9): 1419–1438. doi:10.1038/s41477-023-01491-0. ISSN 2055-0278. PMC 10505561. PMID 37640935.

zygnematophyceae, conjugatophyceae, class, green, algae, paraphylum, streptophyte, algae, also, referred, charophyta, consisting, more, than, 4000, described, species, sister, clade, embryophyta, land, plants, conjugation, spirogyra, scientific, classification. Zygnematophyceae or Conjugatophyceae is a class of green algae in the paraphylum streptophyte algae also referred to as Charophyta 2 consisting of more than 4000 described species 3 The Zygnematophyceae are the sister clade of the Embryophyta land plants 4 5 6 ZygnematophyceaeConjugation in Spirogyra Scientific classification unranked Viridiplantae unranked CharophytaClass ZygnematophyceaeRound 1971SubclassesSubclass Zygnematophycidae Order Zygnematales Order Desmidiales Order Spirogyrales Order Serritaeniales Subclass Spirogloeophycidae Order SpirogloealesSynonyms 1 Akontae Blackman amp Tansley 1902 Conjugatophyceae Engler 1892 Conjugatae Engler 1892 Gamophyceae Saccodermae Pascher ex Kossinskaja 1952 Zygnemaphyceae Round 1971 Zygophyceae Widder 1960Common members of the Zygnematophyceae include the filamentous algae Spirogyra and Mougeotia as well as desmids which are microscopic algae characterized by symmetrical and elaborately ornate cells 7 Contents 1 Morphology 2 Reproduction 3 Taxonomy 3 1 Phylogeny 4 Habitat 5 Fossil record 6 Genomes 7 ReferencesMorphology editThe body plan of Zygnematophyceae is simple and the group appears to have gone through a secondary loss of morphological complexity 8 The most basal members are unicellular but filamentous species have evolved at least five times 9 and a few species form colonies 7 Each cell contains a single nucleus 7 The chloroplasts of the Zygnematophyceae are large typically axile but sometimes parietally located and contain one or several pyrenoids One or several chloroplasts may be present in a single cell The shape of the chloroplast may be star shaped in Zygnema ribbon shaped in Spirogyra or elaborately lobed and dissected In some taxa particularly Mougeotia the chloroplast is able to move in response to different light conditions 7 In the Zygnematophyceae cell walls are composed of three layers one outer layer consisting of mucus a primary wall consisting of microfibrils and an innermost layer of cellulosic microfibrils Some species shed their primary wall and retain only the innermost layer The cell wall may be variously decorated with striations granules or spines In the Desmidiales there are pores in the cell wall which allow the cell to extrude a layer of mucilage for protection 7 Several Zygnematophyceae contain genes involved in protection from desiccation that appear to have been derived by horizontal gene transfer from bacteria the genes are found in plants Zygnematophyceae and bacteria but no other organisms The genes may have helped to enable plants to make the transition to life on land 10 11 A new subclass called Spirogloeophycidae represented by the species Spirogloea muscicola was established after the unicellular subaerial algae resembling a gelatinous blob was rediscovered on a rock close to a river bank near Cologne in 2006 after first being discovered in France in 1845 12 Reproduction editThe Zygnematophyceae are able to reproduce both asexually and sexually Asexual reproduction takes place via fragmentation cell division akinete formation or parthenospores 7 Sexual reproduction in the Zygnematophyceae takes place through a process called conjugation 13 Unusually the gametes lack flagella 7 and they also lack centrioles which suggest that flagella were not secondarily lost This lack of flagella sets the Zygnematophyceae apart from nearly all groups of algae except for red algae and cyanobacteria also known as blue green algae if they are classified as such 1 The gametes are scarcely differentiated from vegetative cells 7 In conjugation cells or filaments of opposite sex line up and tubes form between corresponding cells The male cells then become amoeboid and crawl across the female or sometimes both cells crawl into the connecting tube The cells then meet and fuse to form a zygote which later undergoes meiosis to produce new cells or filaments As in land plants only the female passes its chloroplasts on to the offspring citation needed Taxonomy editThe Zygnematophyceae is monophyletic Traditionally it has been known to contain two orders the Zygnematales and Desmidiales 7 However the Zygnematales were found to be paraphyletic with respect to the Desmidiales and so it was split up As of 2023 update five orders and two subclasses are recognized the Spirogloeales in Spirogloeophycidae and the Serritaeniales the Zygnematales the Spirogyrales and the Desmidiales in Zygnematophycidae 9 Class Zygnematophyceae 14 Subclass Spirogloeophycidae Melkonian Gontcharov amp Marin 2019 11 Order Spirogloeales Melkonian Gontcharov amp Marin 2019 Family Spirogloeaceae Melkonian Gontcharov amp Marin 2019 Subclass Zygnematophycidae Melkonian Gontcharov amp Marin 2019 Order Serritaeniales Hess amp de Vries 2022 Family Serritaeniaceae Hess amp de Vries 2022 Order Zygnematales Borge amp Pascher 1931 Family Zygnemataceae Meneghini Kutzing 1843 Family Mesotaeniaceae Oltmans 1904 paraphyletic Order Spirogyrales Hess amp de Vries 2022 Family Spirogyraceae Palla 1894 Order Desmidiales Krieger 1933 Family Gonatozygaceae Fritsch 1927 Family Closteriaceae Bessey 1907 ex Pritchard 1852 Family Peniaceae Haeckel 1894 Family Desmidiaceae Kutzing 1833b ex Ralfs 1845Phylogeny edit A phylogeny of the families of Zygnematophyceae is presented below 15 11 Zygnematophyceae Spirogloeophycidae Spirogloeales SpirogloeaceaeZygnematophycidae Serritaeniales SerritaeniaceaeZygnematales ZygnemataceaeMesotaeniaceaeSpirogyrales SpirogyraceaeDesmidiales GonatozygaceaeClosteriaceaePeniaceaeDesmidiaceaeHabitat editMembers of the Zygnematophyceae are common in nearly all freshwater habitats particularly filamentous genera such as Spirogyra and Mougeotia Some Spirogyra species can tolerate disturbed habitats On the other hand desmids the Desmidiales often prefer bogs peatlands and lakes 16 Fossil record editVegetative cells of the Zygnematophyceae are fragile and usually not preserved but the zygospores are resistant to decay and can become fossilized The Zygnematophyceae have been recorded from at least the middle Devonian period and before the Carboniferous period all the major groups had diverged Fossils of zygospores are indicators of warming spring conditions and shallow stagnant mesotrophic habitats 7 Genomes editThe first genomes published for Zygnematophyceae were Mesotaenium endlicherianum and Spirogloea muscicola 11 Since then genomes have been published on Penium margaritaceum 17 Zygnema spp 18 and the Closterium peracerosum strigosum littorale complex 19 Furthermore the gene models of Mesotaenium endlicherianum have been updated 20 References edit a b Guiry Michael D 15 March 2013 Taxonomy and nomenclature of the Conjugatophyceae Zygnematophyceae Algae 28 1 1 29 doi 10 4490 algae 2013 28 1 001 hdl 10379 11755 Gontcharov A A Marin B Melkonian M 5 December 2003 Are Combined Analyses Better Than Single Gene Phylogenies A Case Study Using SSU rDNA and rbcL Sequence Comparisons in the Zygnematophyceae Streptophyta Molecular Biology and Evolution 21 3 612 624 doi 10 1093 molbev msh052 PMID 14739253 Pichrtova Martina Holzinger Andreas Kulichova Jana Rysanek David Soljakova Tereza Trumhova Katerina Nemcova Yvonne 8 October 2018 Molecular and morphological diversity of Zygnema and Zygnemopsis Zygnematophyceae Streptophyta from Svalbard High Arctic European Journal of Phycology 53 4 492 508 doi 10 1080 09670262 2018 1476920 PMC 6235541 PMID 30487730 Wickett Norman J Mirarab Siavash Nguyen Nam Warnow Tandy Carpenter Eric Matasci Naim Ayyampalayam Saravanaraj Barker Michael S Burleigh J Gordon Gitzendanner Matthew A Ruhfel Brad R Wafula Eric Der Joshua P Graham Sean W Mathews Sarah Melkonian Michael Soltis Douglas E Soltis Pamela S Miles Nicholas W Rothfels Carl J Pokorny Lisa Shaw A Jonathan DeGironimo Lisa Stevenson Dennis W Surek Barbara Villarreal Juan Carlos Roure Beatrice Philippe Herve dePamphilis Claude W Chen Tao Deyholos Michael K Baucom Regina S Kutchan Toni M Augustin Megan M Wang Jun Zhang Yong Tian Zhijian Yan Zhixiang Wu Xiaolei Sun Xiao Wong Gane Ka Shu Leebens Mack James 11 November 2014 Phylotranscriptomic analysis of the origin and early diversification of land plants Proceedings of the National Academy of Sciences 111 45 E4859 E4868 Bibcode 2014PNAS 111E4859W doi 10 1073 pnas 1323926111 PMC 4234587 PMID 25355905 de Vries Jan Stanton Amanda Archibald John M Gould Sven B June 2016 Streptophyte Terrestrialization in Light of Plastid Evolution Trends in Plant Science 21 6 467 476 doi 10 1016 j tplants 2016 01 021 PMID 26895731 Gitzendanner Matthew A Soltis Pamela S Wong Gane K S Ruhfel Brad R Soltis Douglas E March 2018 Plastid phylogenomic analysis of green plants A billion years of evolutionary history American Journal of Botany 105 3 291 301 doi 10 1002 ajb2 1048 PMID 29603143 a b c d e f g h i j Hall John D McCourt Richard M 2017 Zygnematophyta Handbook of the Protists pp 135 163 doi 10 1007 978 3 319 28149 0 41 ISBN 978 3 319 28149 0 Nishiyama Tomoaki Sakayama Hidetoshi de Vries Jan Buschmann Henrik Saint Marcoux Denis Ullrich Kristian K Haas Fabian B Vanderstraeten Lisa Becker Dirk Lang Daniel Vosolsobe Stanislav Rombauts Stephane Wilhelmsson Per K I Janitza Philipp Kern Ramona Heyl Alexander Rumpler Florian Villalobos Luz Irina A Calderon Clay John M Skokan Roman Toyoda Atsushi Suzuki Yutaka Kagoshima Hiroshi Schijlen Elio Tajeshwar Navindra Catarino Bruno Hetherington Alexander J Saltykova Assia Bonnot Clemence Breuninger Holger Symeonidi Aikaterini Radhakrishnan Guru V Van Nieuwerburgh Filip Deforce Dieter Chang Caren Karol Kenneth G Hedrich Rainer Ulvskov Peter Glockner Gernot Delwiche Charles F Petrasek Jan Van de Peer Yves Friml Jiri Beilby Mary Dolan Liam Kohara Yuji Sugano Sumio Fujiyama Asao Delaux Pierre Marc Quint Marcel Theissen Gunter Hagemann Martin Harholt Jesper Dunand Christophe Zachgo Sabine Langdale Jane Maumus Florian Van Der Straeten Dominique Gould Sven B Rensing Stefan A July 2018 The Chara Genome Secondary Complexity and Implications for Plant Terrestrialization Cell 174 2 448 464 e24 doi 10 1016 j cell 2018 06 033 PMID 30007417 S2CID 206569169 a b Hess Sebastian Williams Shelby K Busch Anna Irisarri Iker Delwiche Charles F Vries Sophie de Darienko Tatyana Roger Andrew J Archibald John M Buschmann Henrik Schwartzenberg Klaus von Vries Jan de 2022 09 01 A phylogenomically informed five order system for the closest relatives of land plants Current Biology 32 20 4473 4482 e7 doi 10 1016 j cub 2022 08 022 ISSN 0960 9822 PMC 9632326 PMID 36055238 Zimmer Carl 14 November 2019 How Did Plants Conquer Land These Humble Algae Hold Clues The New York Times a b c d Cheng Shifeng Xian Wenfei Fu Yuan Marin Birger Keller Jean Wu Tian Sun Wenjing Li Xiuli Xu Yan Zhang Yu Wittek Sebastian Reder Tanja Gunther Gerd Gontcharov Andrey Wang Sibo Li Linzhou Liu Xin Wang Jian Yang Huanming Xu Xun Delaux Pierre Marc Melkonian Barbara Wong Gane Ka Shu Melkonian Michael 2019 Genomes of Subaerial Zygnematophyceae Provide Insights into Land Plant Evolution Cell 179 5 1057 1067 e14 doi 10 1016 j cell 2019 10 019 PMID 31730849 Ancient plants learned to survive on land by stealing other species DNA Kapraun D F 30 November 2006 Nuclear DNA Content Estimates in Green Algal Lineages Chlorophyta and Streptophyta Annals of Botany 99 4 677 701 doi 10 1093 aob mcl294 PMC 2802934 PMID 17272304 Guiry M D Guiry G M Zygnematophyceae AlgaeBase World wide electronic publication National University of Ireland Galway Retrieved 2023 04 30 Stancheva Rosalina Hall John D Herburger Klaus Lewis Louise A Mccourt Richard M Sheath Robert Holzinger Andreas July 2014 Phylogenetic position of Zygogonium ericetorum Zygnematophyceae Charophyta from a high alpine habitat and ultrastructural characterization of unusual aplanospores Journal of Phycology 50 5 790 803 doi 10 1111 jpy 12229 PMC 4370237 PMID 25810560 Hall John D McCourt Richard M 2014 Chapter 9 Conjugating Green Algae Including Desmids In Wehr John D Sheath Robert G Kociolek J 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