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Centrohelid

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Centrohelids
Raphidiophrys contractilis
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
Phylum: Haptista
Class: Centroplasthelida
Febvre‐Chevalier & Febvre, 1984[1]
Orders[1][2]

Incertae sedis

Synonyms
  • Centroplastiales
  • Centrohelina Hartmann 1913
  • Centroheliozoa Cushman & Jarvis 1929 sensu Durrschmidt & Patterson 1987
  • Centrohelida Kühn 1926[3]
  • Centrohelea Kuhn 1926 stat. n. Cavalier-Smith 1993

The centrohelids or centroheliozoa are a large group of heliozoan protists.[4] They include both mobile and sessile forms, found in freshwater and marine environments, especially at some depth.[clarification needed]

Characteristics

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Individuals are unicellular and spherical, usually around 30–80 μm in diameter, and covered with long radial axopods, narrow cellular projections that capture food and allow mobile forms to move about.

A few genera have no cell covering, but most have a gelatinous coat holding scales and spines, produced in special deposition vesicles. These may be organic or siliceous and come in various shapes and sizes. For instance, in Raphidiophrys the coat extends along the bases of the axopods, covering them with curved spicules that give them a pine-treeish look, and in Raphidiocystis there are both short cup-shaped spicules and long tubular spicules that are only a little shorter than the axopods. Some other common genera include Heterophrys, Actinocystis, and Oxnerella.

The axopods of centrohelids are supported by microtubules in a triangular-hexagonal array, which arise from a tripartite granule called the centroplast at the center of the cell. Axopods with a similar array occur in gymnosphaerids, which have traditionally been considered centrohelids (though sometimes in a separate order from the others). This was questioned when it was found they have mitochondria with tubular cristae, as do other heliozoa, while in centrohelids the cristae are flat. Although this is no longer considered a very reliable character, on balance gymnosphaerids seem to be a separate group.

Representation of a centrohelid
  1. Axopod
  2. Microtubule bundle
  3. Kinetocysts, probably help to paralyze prey
  4. Contractile vacuole, regulates the quantity of water inside a cell
  5. Lipid globule
  6. Lysosome, holds enzymes
  7. Phagocytic vesicle
  8. Golgi apparatus layer, modifies proteins and sends them out of the cell
  9. Exclusion zone
  10. Centroplast
  11. Central granule
  12. Scales
  13. Spicule-forming organelle, spicules are the needle-shaped spines on the surface[5]
  14. Silica deposition vesicle
  15. Digestive vesicle
  16. Nucleolus
  17. Nucleus
  18. Prekinetocyst
  19. Mitochondrion, creates ATP (energy) for the cell (ribbon shaped cristae)
  20. Prey
  21. Endoplasm
  22. Ectoplasm


Taxonomy

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History

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The evolutionary position of the centrohelids is not clear. Structural comparisons with other groups are difficult, in part because no flagella occur among centrohelids, and genetic studies have been more or less inconclusive. Cavalier-Smith has suggested they may be related to the Rhizaria,[6] but for the most part they are left with uncertain relations to other groups. A 2009 paper suggests that they may be related to the cryptophytes and haptophytes (see Cryptomonads-haptophytes assemblage).[7] They are currently classified as Hacrobia, under the Plants+HC clade, although some research studies have found evidence against the monophyly of this group.[8] Centrohelids were previously divided into two orders with contrasting scale morphology and ultrastructure: Pterocystida and Acanthocystida.[9] Posterior molecular studies of 2018 have rearranged the classification of centrohelids into two taxa: Pterocystida and Panacanthocystida, which includes both Acanthocystida and the genus Yogsothoth.[2][1]

Classification

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The modern classification of centrohelids, as of 2019:[2][1]

Notes

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  1. ^ Heteroraphidiophrys, mentioned by Mikrjukov in 2002, was never formally introduced and needs to be avoided; the organism designated needs to be re‐isolated, carefully studied and provided with formal description.[1]

References

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  1. ^ a b c d e Adl SM, Bass D, Lane CE, Lukeš J, Schoch CL, Smirnov A, Agatha S, Berney C, Brown MW, Burki F, Cárdenas P, Čepička I, Chistyakova L, del Campo J, Dunthorn M, Edvardsen B, Eglit Y, Guillou L, Hampl V, Heiss AA, Hoppenrath M, James TY, Karnkowska A, Karpov S, Kim E, Kolisko M, Kudryavtsev A, Lahr DJG, Lara E, Le Gall L, Lynn DH, Mann DG, Massana R, Mitchell EAD, Morrow C, Park JS, Pawlowski JW, Powell MJ, Richter DJ, Rueckert S, Shadwick L, Shimano S, Spiegel FW, Torruella G, Youssef N, Zlatogursky V, Zhang Q (2019). "Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes". Journal of Eukaryotic Microbiology. 66 (1): 4–119. doi:10.1111/jeu.12691. PMC 6492006. PMID 30257078.
  2. ^ a b c Shɨshkin, Yegor; Drachko, Daria; Klimov, Vladimir I.; Zlatogursky, Vasily V. (November 2018). "Yogsothoth knorrus gen. n., sp. n. and Y. carteri sp. n. (Yogsothothidae fam. n., Haptista, Centroplasthelida), with notes on evolution and systematics of centrohelids". Protist. 169 (5): 682–696. doi:10.1016/j.protis.2018.06.003.
  3. ^ Kühn, A. (1926). Morphologie der Tiere in Bildern. Heft 2: Protozoen. Teil 2. Rhizopoden. Gebrüder Borntraeger: Berlin.
  4. ^ Nikolaev SI; Berney C; Fahrni JF; et al. (May 2004). "The twilight of Heliozoa and rise of Rhizaria, an emerging supergroup of amoeboid eukaryotes". Proc. Natl. Acad. Sci. U.S.A. 101 (21): 8066–8071. doi:10.1073/pnas.0308602101. PMC 419558. PMID 15148395.
  5. ^ Zlatogursky, Vasily V. (February 2016). "There and Back Again: Parallel Evolution of Cell Coverings in Centrohelid Heliozoans". Protist. 167 (1): 51–66. Retrieved 2024-11-02.
  6. ^ Cavalier-Smith T, Chao EE (April 2003). "Molecular phylogeny of centrohelid heliozoa, a novel lineage of bikont eukaryotes that arose by ciliary loss". J. Mol. Evol. 56 (4): 387–396. Bibcode:2003JMolE..56..387C. doi:10.1007/s00239-002-2409-y. PMID 12664159. S2CID 8007933.
  7. ^ Burki, F; Inagaki, Y; Bråte, J; Archibald, J.; Keeling, P.; Cavalier-Smith, T; Sakaguchi, M; Hashimoto, T; Horak, A; Kumar, S; Klaveness, D; Jakobsen, K.S; Pawlowski, J; Shalchian-Tabrizi, K (2009). "Large-scale phylogenomic analyses reveal that two enigmatic protist lineages, Telonemia and Centroheliozoa, are related to photosynthetic chromalveolates". Genome Biology and Evolution. 1: 231–238. doi:10.1093/gbe/evp022. PMC 2817417. PMID 20333193.
  8. ^ Zhao, Sen; Burki, Fabien; Bråte, Jon; Keeling, Patrick J.; Klaveness, Dag; Shalchian-Tabrizi, Kamran (2012). "Collodictyon—An Ancient Lineage in the Tree of Eukaryotes". Molecular Biology and Evolution. 29 (6): 1557–68. doi:10.1093/molbev/mss001. PMC 3351787. PMID 22319147.
  9. ^ Cavalier-Smith, Thomas; Chao, Ema E. (2012). "Oxnerella micra sp. n. (Oxnerellidae fam. n.), a Tiny Naked Centrohelid, and the Diversity and Evolution of Heliozoa". Protist. 163 (4): 574–601. doi:10.1016/j.protis.2011.12.005. PMID 22317961.

Further reading

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