Glissomonadida | |
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The glissomonad Orciraptor agilis attacking an Actinotaenium cell. | |
Scientific classification | |
Domain: | Eukaryota |
Clade: | Diaphoretickes |
Clade: | SAR |
Phylum: | Cercozoa |
Class: | Sarcomonadea |
Subclass: | Pediglissa |
Order: | Glissomonadida Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009[1] emend. Hess & Melkonian, 2013 |
Suborders & families[2] | |
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The glissomonads are a group of bacterivorous gliding flagellated protists that compose the order Glissomonadida, in the amoeboflagellate phylum Cercozoa.[1] They comprise a vast, largely undescribed diversity of soil and freshwater organisms.[3] They are the sister group to cercomonads; the two orders form a solid clade of gliding soil-dwelling flagellates called Pediglissa.[2]
Morphology
External appearance
Glissomonads are zooflagellates that aren't strongly amoeboid, and are only covered by a plasma membrane. Their common ancestor is thought to be a biflagellate, with a short anterior flagellum and a long posterior flagellum, that glided on the substrate by moving their posterior flagellum. In gliding descendants, the cell's posterior zone is usually rounded, giving the cell an ovoid shape. Some species may temporarily extend a protoplasmic tail, that unlike most cercomonads doesn't trail along the posterior flagellum.[1] At least two genera, Orciraptor and Viridiraptor, are capable of transforming into a distinctly amoeboid state attached to the surface.[4]
The group also includes descendants that have lost their gliding, mainly Proleptomonas. This genus has another exception to the group: an anterior flagellum that is longer than the posterior, while the posterior is adherent to the cell and not used for gliding.[1]
Internal structure
Most species lack obvious morphological specializations: there is no cytopharynx, deep flagellar groove, or pocket evident. Apart from Proleptomonas, which is exceptionally elongated and has a modified cytoskeleton, the nucleus is usually anterior and attached to the kinetid (= flagellar apparatus) through well-developed fibrous roots. There are typically two posterior and one anterior microtubular centriolar roots. A contractile vacuole is usually seen in the cell's posterior area. The mitochondria have tubular cristae. There is a microbody attached to the posterior side of the nucleus, except in Proleptomonas. The Golgi apparatus is usually seen associated with the nucleus, which doesn't happen in all cercozoans.[1]
Both flagella have the same thickness and are simple, without a paraxonemal rod, hairs or scales, sometimes acronematic (= with an acroneme). Unlike in cercomonads, the ciliary transition zone has a dense transverse plate at the distal end. The anterior flagellum beats like a cilium towards the left, as seen in cercomonads, and is sometimes reduced to a short stub without an axoneme.[1]
Ecology and behavior
Glissomonads are heterotrophic aerobic organisms that almost exclusively inhabit soil or freshwater, where they feed on bacteria.[3] Sexual reproduction is unknown. Cysts are present in the group, and have smooth walls.[1]
Phylogeny
The cladogram below depicts the evolutionary relationships between most of the glissomonad families:[5]
Glissomonadida |
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Classification
The current classification is:[2]
- Family Saccharomycomorphidae Feng, He, Jiang, Zhang & Yu, 2021[5]
- Suborder Allapsina Cavalier-Smith, 2018
- Family Allapsidae Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Allapsa Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Allantion Sandon, 1924
- Teretomonas Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Family Allapsidae Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Suborder Sandonina Cavalier-Smith, 2018
- Family Dujardinidae Cavalier-Smith & Howe, 2011
- Dujardina Cavalier-Smith & Howe, 2011
- Family Bodomorphidae Hollande, 1952
- Bodomorpha Hollande, 1942
- Family Sandonidae Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Flectomonas Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Mollimonas Howe & Cavalier-Smith, 2011
- Neoheteromita Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Sandona Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Family Proleptomonadidae Howe, Bass, Vickerman, Chao & Cavalier-Smith, 2009
- Proleptomonas Woodcock, 1916
- Family Dujardinidae Cavalier-Smith & Howe, 2011
- Suborder Pansomonadina Vickerman, 2005 stat. nov. Cavalier-Smith, 2018
- Family Viridiraptoridae Hess & Melkonian, 2013
- Viridiraptor Hess & Melkonian, 2013
- Orciraptor Hess & Melkonian, 2013
- Family Agitatidae Cavalier-Smith & Bass, 2009
- Agitata Cavalier-Smith & Bass, 2009
- Family Acinetactidae Stokes, 1886
- Acinetactis Stokes, 1886
- Family Aurigamonadidae Cavalier-Smith, 2011
- Aurigamonas Vickerman, 2005
- Family Viridiraptoridae Hess & Melkonian, 2013
References
- 1 2 3 4 5 6 7 Howe AT, Bass D, Vickerman K, Chao EE, Cavalier-Smith T (2009). "Phylogeny, Taxonomy, and Astounding Genetic Diversity of Glissomonadida ord. nov., The Dominant Gliding Zooflagellates in Soil (Protozoa: Cercozoa)". Protist. 160 (2): 159–189. doi:10.1016/j.protis.2008.11.007. ISSN 1434-4610.
- 1 2 3 Cavalier-Smith, Thomas; Chao, Ema E.; Lewis, Rhodri (April 2018). "Multigene phylogeny and cell evolution of chromist infrakingdom Rhizaria: contrasting cell organisation of sister phyla Cercozoa and Retaria". Protoplasma. 255 (5): 1517–1574. doi:10.1007/s00709-018-1241-1. PMC 6133090. PMID 29666938.
- 1 2 Howe AT, Bass D, Chao EE, Cavalier-Smith T (2011). "New Genera, Species, and Improved Phylogeny of Glissomonadida (Cercozoa)". Protist. 162 (5): 710–722. doi:10.1016/j.protis.2011.06.002. ISSN 1434-4610.
- ↑ Hess S, Melkonian M (2013). "The Mystery of Clade X: Orciraptor gen. nov. and Viridiraptor gen. nov. are Highly Specialised, Algivorous Amoeboflagellates (Glissomonadida, Cercozoa)". Protist. 164 (5): 706–747. doi:10.1016/j.protis.2013.07.003. ISSN 1434-4610.
- 1 2 Feng, Jian-Ju; He, Chen-Yang; Jiang, Shu-Hua; Zhang, Tao; Yu, Li-Yan (2021). "Saccharomycomorpha psychra n. g., n. sp., a Novel Member of Glissmonadida (Cercozoa) Isolated from Arctic and Antarctica". Journal of Eukaryotic Microbiology. 68 (3). doi:10.1111/jeu.12840.