Biology:Lophotrochozoa

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Short description: Superphylum of animals

Lophotrochozoa
Temporal range: 536–0 Ma[1]
Caribbean reef squid.jpg
Caribbean reef squid or Sepioteuthis sepioidea is a complex lophotrochozoan
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Subkingdom: Eumetazoa
Clade: ParaHoxozoa
Clade: Bilateria
Clade: Nephrozoa
(unranked): Protostomia
(unranked): Spiralia
Superphylum: Lophotrochozoa
Halanych et al., 1995
Phyla

Lophotrochozoa (/ləˌfɒtrkˈzə/, "crest/wheel animals") is a clade of protostome animals within the Spiralia. The taxon was established as a monophyletic group based on molecular evidence.[2][3] The clade includes animals like annelids, molluscs, bryozoans, brachiopods, and platyhelminthes.[4]

Groups

Lophotrochozoa was defined in 1995 as the "last common ancestor of the three traditional lophophorate taxa (brachiopods, bryozoans, and phoronid worms), the mollusks and the annelids, and all of the descendants of that common ancestor".[5] It is a cladistic definition (a node-based name), so the affiliation to Lophotrochozoa of spiralian groups not mentioned directly in the definition depends on the topology of the spiralian tree of life, and in some phylogenetic hypotheses, Lophotrochozoa may even be synonymous to Spiralia. Nemertea and Orthonectida (if not directly considered as part of Annelida) are probably lophotrochozoan phyla; Dicyemida, Gastrotricha, and Platyhelminthes may be lophotrochozoans or placed in the Rouphozoa clade outside Lophotrochozoa; Chaetognatha, Gnathostomulida, Micrognathozoa, and Syndermata are probably gnathiferans and so placed as a basal spiralian clade outside Lophotrochozoa; Cycliophora could be a gnathiferan or a lophotrochozoan phylum. One of the candidate hypotheses is presented below.

The Lophotrochozoa has basal Cycliophora and Mollusca groups, and more derived Lophophorate, Nemertea and Annelida groups.[6][7]

With the introduction of Platytrochozoa and Rouphozoa, one candidate phylogeny is pictured below – though other studies recover a range of alternative possibilities:[8][9][10][11][12][13][14][15]

In the most recent research, the three phyla Cycliophora, Entoprocta and Bryozoa makes up a single clade and are the first to branch off from the other lophotrochozoans. The second split is the molluscs, and the third consists of two sister phyla, annelids and nemerteans. Lastly remains the clade that consist of the phoronids and the brachiopods.[16][17]

Protostomes

Ecdysozoa Long nosed weevil edit.jpg

Spiralia

Gnathifera Chaetoblack 3.png

Platytrochozoa
Rouphozoa

Gastrotricha Lepidodermella squamatum (cropped).jpg

Platyhelminthes Sorocelis reticulosa.jpg

Mesozoa EB1911 Mesozoa - Rhopalura giardii.jpg

Lophotrochozoa

Cycliophora Symbion pandora (unlabelled).jpg

Annelida

Echiura Ochetostoma erythrogrammon sujiyumusi (cropped).jpg

Clitellata Polychaeta (no) 2.jpg

Siboglinidae Riftia tube worms Galapagos 2011.jpg

Sipuncula Themiste petricola, everted.jpg

Mollusca Grapevinesnail 01.jpg

Kryptotrochozoa
Lophophorata
Brachiozoa

Brachiopoda Lingula sp. (brachiopod shell) (modern; Masbate, Philippines) 2 (rotated).jpg

Phoronida Nur03506.jpg

Bryozoa s.l.

Entoprocta Pedicellina cernua 001.png

Ectoprocta Plumatella repens from Haeckel Bryozoa drawing Commons2.jpg

Nemertea Micrura verrilli Coe, 1901.png

Another study recovers Lophotrochozoa as equivalent to Platytrochozoa, forming a sister group with Gnathifera at the base of Spiralia.[18]


A number of fossil taxa can be identified as early Lophotrochozoans, even if their precise affinity remains contested. However, relevant Cambrian fossils are debated.

Characteristics

The clade Lophotrochozoa is named after the two distinct characteristics of its members; the lophophore, a feeding structure consisting of a ciliated crown of tentacles surrounding a mouth, and the developmental stage of the trochophore larva. Lophophorata such as Brachiozoa and Bryozoa have lophophores, while members of Trochozoa such as molluscs and annelids have trochophore larvae, although some may have none.[19][20]

References

  1. Budd, Graham E.; Jackson, Illiam S. C. (January 5, 2016). "Ecological innovations in the Cambrian and the origins of the crown group phyla". Philosophical Transactions of the Royal Society B: Biological Sciences 371 (1685): 20150287. doi:10.1098/rstb.2015.0287. PMID 26598735. 
  2. Halanych, K. M.; Bacheller, J.; Liva, S.; Aguinaldo, A. A.; Hillis, D. M.; Lake, J. A. (17 March 1995). "18S rDNA evidence that the Lophophorates are Protostome Animals". Science 267 (5204): 1641–1643. doi:10.1126/science.7886451. PMID 7886451. 
  3. Hervé, Philippe; Lartillot, Nicolas; Brinkmann, Henner (May 2005). "Multigene Analyses of Bilaterian Animals Corroborate the Monophyly of Ecdysozoa, Lophotrochozoa, and Protostomia". Molecular Biology and Evolution 22 (5): 1246–1253. doi:10.1093/molbev/msi111. PMID 15703236. 
  4. Halanych, K. M. (2016-01-01), Kliman, Richard M., ed., Lophotrochozoa, Diversification of, Oxford: Academic Press, pp. 405–408, doi:10.1016/b978-0-12-800049-6.00272-9, ISBN 978-0-12-800426-5, https://www.sciencedirect.com/science/article/pii/B9780128000496002729, retrieved 2021-02-14 
  5. Halanych, Kenneth M.; Bacheller, John D.; Aguinaldo, Anna Marie A.; Liva, Stephanie M.; Hillis, David M.; Lake, James A. (1995-03-17). "Evidence from 18S ribosomal DNA that the lophophorates are protostome animals". Science (American Association for the Advancement of Science) 267 (5204): 1642. doi:10.1126/science.7886451. ISSN 1095-9203. PMID 7886451. Bibcode1995Sci...267.1641H. https://www.researchgate.net/publication/6049932. Retrieved 2021-02-16. 
  6. Nesnidal, Maximilian P; Helmkampf, Martin; Meyer, Achim; Witek, Alexander; Bruchhaus, Iris; Ebersberger, Ingo; Hankeln, Thomas; Lieb, Bernhard et al. (2013). "New phylogenomic data support the monophyly of Lophophorata and an Ectoproct-Phoronid clade and indicate that Polyzoa and Kryptrochozoa are caused by systematic bias". BMC Evolutionary Biology 13 (1): 253. doi:10.1186/1471-2148-13-253. PMID 24238092. 
  7. Laumer, Christopher E.; Bekkouche, Nicolas; Kerbl, Alexandra; Goetz, Freya; Neves, Ricardo C.; Sørensen, Martin V.; Kristensen, Reinhardt M.; Hejnol, Andreas et al. (August 2015). "Spiralian Phylogeny Informs the Evolution of Microscopic Lineages". Current Biology 25 (15): 2000–2006. doi:10.1016/j.cub.2015.06.068. PMID 26212884. 
  8. Paps, Jordi; Baguñà, Jaum; Riutort, Marta (2009-10-01). "Bilaterian Phylogeny: A Broad Sampling of 13 Nuclear Genes Provides a New Lophotrochozoa Phylogeny and Supports a Paraphyletic Basal Acoelomorpha". Molecular Biology and Evolution 26 (10): 2397–2406. doi:10.1093/molbev/msp150. PMID 19602542. 
  9. Struck, Torsten H.; Schult, Nancy; Kusen, Tiffany; Hickman, Emily; Bleidorn, Christoph; McHugh, Damhnait; Halanych, Kenneth M (5 April 2007). "Annelid phylogeny and the status of Sipuncula and Echiura". BMC Evolutionary Biology 7 (1): 57. doi:10.1186/1471-2148-7-57. PMID 17411434. 
  10. Hausdorf, Bernhard; Helmkampf, Martin; Meyer, Achim; Witek, Alexander; Herlyn, Holger; Bruchhaus, Iris; Hankeln, Thomas; Struck, Torsten H. et al. (2007-12-01). "Spiralian Phylogenomics Supports the Resurrection of Bryozoa Comprising Ectoprocta and Entoprocta". Molecular Biology and Evolution 24 (12): 2723–2729. doi:10.1093/molbev/msm214. PMID 17921486. 
  11. Struck, Torsten H.; Wey-Fabrizius, Alexandra R.; Golombek, Anja; Hering, Lars; Weigert, Anne; Bleidorn, Christoph; Klebow, Sabrina; Iakovenko, Nataliia et al. (July 2014). "Platyzoan Paraphyly Based on Phylogenomic Data Supports a Noncoelomate Ancestry of Spiralia". Molecular Biology and Evolution 31 (7): 1833–1849. doi:10.1093/molbev/msu143. PMID 24748651. 
  12. "cycliophorans". http://eol.org/pages/1922/details. 
  13. Lu, Tsai-Ming; Kanda, Miyuki; Satoh, Noriyuki; Furuya, Hidetaka (29 May 2017). "The phylogenetic position of dicyemid mesozoans offers insights into spiralian evolution". Zoological Letters 3 (1): 6. doi:10.1186/s40851-017-0068-5. PMID 28560048. 
  14. Temereva, Elena N.; Kuzmina, Tatyana V. (31 July 2017). "The first data on the innervation of the lophophore in the rhynchonelliform brachiopod Hemithiris psittacea: what is the ground pattern of the lophophore in lophophorates?". BMC Evolutionary Biology 17 (1): 172. doi:10.1186/s12862-017-1029-5. PMID 28760135. 
  15. Luo, Yi-Jyun; Kanda, Miyuki; Koyanagi, Ryo; Hisata, Kanako; Akiyama, Tadashi; Sakamoto, Hirotaka; Sakamoto, Tatsuya; Satoh, Noriyuki (4 December 2017). "Nemertean and phoronid genomes reveal lophotrochozoan evolution and the origin of bilaterian heads". Nature Ecology & Evolution 2 (1): 141–151. doi:10.1038/s41559-017-0389-y. PMID 29203924. 
  16. Polyzoa is back: The effect of complete gene sets on the placement of Ectoprocta and Entoprocta
  17. Phyla of Tiny Filter Feeders Find a New Spot on the Tree of Life
  18. Marlétaz, Ferdinand; Peijnenburg, Katja T. C. A.; Goto, Taichiro; Satoh, Noriyuki; Rokhsar, Daniel S. (2019-01-10). "A New Spiralian Phylogeny Places the Enigmatic Arrow Worms among Gnathiferans". Current Biology 29 (2): 312–318.e3. doi:10.1016/j.cub.2018.11.042. ISSN 0960-9822. PMID 30639106. 
  19. Barnes, Robert D. (1982). Invertebrate Zoology. Saunders College. pp. 200–206. ISBN 978-0-03-056747-6. OCLC 1015202568. 
  20. Reece, Jane B.; Urry, Lisa A.; Cain, Michael L. (2013). Campbell Biology. Berkeley, California: Pearson. p. 688. ISBN 978-0-321-77565-8. 

Further reading

Wikidata ☰ Q321481 entry