Pyrenomonadaceae

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Pyrenomonadaceae
Rhodomonas salina CCMP 322.jpg
Rhodomonas salina
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Pyrenomonadaceae

Novarino & Lucas 1993
Genera

Pyrenomonadaceae is a family of cryptomonads which includes three or four known genera. They are distinguished from other cryptomonads by their nucleomorphs being imbedded into the pyrenoid, and the presence of distinctive pigment phycoerythrin 545. [1]

Contents

Taxonomy

Rhodomonas was the first genus within today's Pyrenomonadaceae identified, being described in 1898. [2] For most of the 20th century, all other genera now recognized as Pyrenomonadaceae were placed into various other taxa (ex. Rhinomonas fulva as Cryptochrysis fulva) [3] Adolf Pascher placed Rhodomonas within his subfamily Cryptochrysideae in 1913. [4] Butcher's highly influential 1967 phylogeny of all then-known Cryptophytes did not recognize Rhodomonas, reclassifying all previously described Rhodomonas species as Chroomonas . [5]

Between 1982 and 1986, a series of ultrastructure studies by Uwe J. Santore found considerable morphological inconsistencies within Butcher's Chroomonas, leading him to identify the new genus Pyrenomonas in 1984. [6] [7] Two years later, he revived genus Rhodomonas and proposed the existence of a clade largely consisting of "reddish-brown cryptomonads". [8] [9] Expanding upon Santore's research, in 1988 D.R.A. Hill and R. Wetherbee analyzed various cryptomonads that had been treated as Cryptochrysis by early 20th century researchers. From this they identified several new species of Rhodomonas, and introduced the new genus Rhinomonas . [3] Hill would identify another "reddish-brown cryptomonad" genus in 1991, Storeatula . [10] In 1989, Hill and Wetherbee argued that Rhodomonas was synonymous with Pyrenomonas, triggering an academic debate regarding whether or not each genus should be treated separately. [11] This debate remains unresolved as of 2019. [12]

The earliest reference to Pyrenomonadaceae in an approximately modern sense was made by Gianfranco Novarino and Ian Lucas in their 1993 classification scheme for the Cryptophyceae. [1] In this classification scheme, the family included Rhinomonas and Pyrenomonas. An updated scheme in 1999 added Storeatula as well. [13]

Overall monophyly of the Pyrenomonadaceae has been universally supported by electron-microscope and molecular-based studies in the 1990s and 2000s. [12] A 2002 phylogenic study of 18s rDNA suggested that, while the family itself was monophyletic, Rhodomonas was not, with R. abbreviata forming a clade with Storeatula while all other Rhodomonas species examined formed a clade with Rhinomonas. [14] A more comprehensive phylogenetic study in 2014 largely agreed with and expanded upon earlier findings, presenting a preliminary classification scheme with three unnamed clades. [15]

Clay et al, 1999

Pyrenomonadaceae

Rhinomonas

Pyrenomonas

Storeatula

Deane et al, 2002

"Clade E" Cryptomonads

Rhodomonas sp.

Rhodomonas maculata

Rhodomonas marina

Rhinomonas

Pyrenomonas

Storeatula

Rhodomonas abbreviata

Majaneva et al, 2014

Pyrenomonadaceae

Rhodomonas duplex

Rhodomonas marina

Storeatula sp.

Rhodomonas abbreviata

Rhodomonas lens

Rhodomonas sp.

Rhodomonas baltica

Rhodomonas sp.

Rhinomonas pauca

Storeatula major

Rhinomonas reticulata

Rhinomonas nottbecki

Related Research Articles

Cryptomonad Subphylum of algae

The cryptomonads are a group of algae, most of which have plastids. They are common in freshwater, and also occur in marine and brackish habitats. Each cell is around 10–50 μm in size and flattened in shape, with an anterior groove or pocket. At the edge of the pocket there are typically two slightly unequal flagella.

Cryptomonas is the name-giving genus of the Cryptomonads established by German biologist Christian Gottfried Ehrenberg in 1831. The algae are common in freshwater habitats and brackish water worldwide and often form blooms in greater depths of lakes. The cells are usually brownish or greenish in color and are characteristic of having a slit-like furrow at the anterior. They are not known to produce any toxins. They are used to feed small zooplankton, which is the food source for small fish in fish farms. Many species of Cryptomonas can only be identified by DNA sequencing. Cryptomonas can be found in several marine ecosystems in Australia and South Korea.

<i>Gymnodinium</i> Genus of single-celled organisms

Gymnodinium is a genus of dinoflagellates, a type of marine and freshwater plankton. It is one of the few naked dinoflagellates, or species lacking armor known as ellulosic plates. Since 2000, the species which had been considered to be part of Gymnodinium have been divided into several genera, based on the nature of the apical groove and partial LSU rDNA sequence data. Amphidinium was redefined later. Gymnodinium belong to red dinoflagellates that, in concentration, can cause red tides.

Cryptophyceae Class of single-celled organisms

The cryptophyceae are a class of algae, most of which have plastids. About 220 species are known, and they are common in freshwater, and also occur in marine and brackish habitats. Each cell is around 10–50 μm in size and flattened in shape, with an anterior groove or pocket. At the edge of the pocket there are typically two slightly unequal flagella.

Astrephomene is a genus of green algae in the family Goniaceae, order Chlamydomonadales. The genus was first described in 1937 by Pocock and named by Pockock in 1953.

Goniaceae Family of algae

Goniaceae is a family of algae in the order Chlamydomonadales, that includes the genera Astrephomene and Gonium. Members of the Goniaceae are distinguished from those of the Volvocaceae by having each cell surrounded by a tripartite boundary of the extracellular matrix, as opposed to the entire colony being surrounded by the tripartite boundary in Volvocaceae.

<i>Rhodomonas</i> Genus of single-celled organisms

Rhodomonas is a genus of cryptomonads.

Geminigera /ˌdʒɛmɪnɪˈdʒɛɹə/ is a genus of cryptophyte from the family Geminigeraceae. Named for its unique pyrenoids, Geminigera is a genus with a single mixotrophic species. It was discovered in 1968 and is known for living in very cold temperatures such as under the Antarctic ice. While originally considered to be part of the genus Cryptomonas, the genus Geminigera was officially described in 1991 by D. R. A. Hill.

Plagioselmis is a genus of cryptophytes, including the species Plagioselmis punctata.

<i>Pediastrum duplex</i> Species of alga

Pediastrum duplex is a species of fresh water green algae in the genus Pediastrum.

Batrachospermaceae Family of algae

Batrachospermaceae is a family of fresh water red algae (Rhodophyta). Genera within the Batrachospermaceae generally have a "Lemanea-type" life history with carpospores germinating to produce chantransia. Sporophyte phase with meiosis occurs in an apical cell to produce the gametophyte stage. Pit connections have two pit plug cap layers with the other layer enlarged. This family of freshwater red algae is uniaxial, meaning each filament with a single apical cell. The genera included within Batrachospermaceae are listed in the table below.

Tetragonidiaceae is a family of cryptomonads which includes two genera. Members of Tetragonidiaceae are distinguished from other cryptomonads by reproduction occurring in a non-motile vegetative phase, as well as the formation of multicellular filaments unlike any other cryptomonad family.

Chroomonadaceae is a family of cryptomonads first recognized by Clay et al in 1999 as including genera Chroomonas, Falcomonas, and Komma. Following a molecular phylogenic study in 2002, Hemiselmis was also placed within the Chroomonadaceae. Today, the family is generally recognized as sister to the Pyrenomonadaceae.

Hilleaceae was one of the three families of Cryptomonads proposed by R.W. Butcher in 1967, who included only the genus Hillea. It has appeared in at least two other cryptomonad classification systems since then. However, as Hillea has yet to be successfully cultured, its validity as a genus remains uncertain.

Cryptochrysis is a formerly recognized genus of cryptomonads first proposed by Adolf Pascher in 1911. He initially treated it as the sole genus in family Cryptochrysidaceae, but later treated it as a member of the Cryptochrysideae subfamily of Cryptomonadaceae, along with Rhodomonas, Chroomonas, and Cyanomonas. In 1967, R.W. Butcher relegated the group to a subgenus within Chroomonas.

Bjornbergiella hawaiiensis is a Hawaiian species of cryptomonad described in 1965. It is the sole member of the genus Bjornbergiella.

Rhinomonas lateralis is a species of cryptomonad given its current designation in 1988.

Timothy John Entwisle Australian botanist, much of

Timothy John Entwisle, is an Australian botanist, much of whose research work is in phycology (algae). See for example the articles. He was awarded a Ph.D. from La Trobe University in 1986 for work on the taxonomy of Vaucheria.

Greta Albrecht Fryxell was a marine scientist known for her work on the biology and taxonomy of diatoms. In 1996, she was elected a fellow of the American Association for the Advancement of Science.

Linda Karen Medlin is a molecular biologist known for her work on diatoms. She is an elected member of the Norwegian Academy of Science and Letters.

References

  1. 1 2 Novarino and Lucas (1993), "Some proposals for a new classification system of the Cryptophyceae", Botanical Journal of the Linnean Society, 111 (1): 3–21, doi:10.1006/bojl.1993.1002
  2. Karsten G (1898). "Rhodomonas baltica, n.g. et sp". 3. Wissenschaftliche Meeresuntersuchungen, Abteilung Kiel: 15–16.{{cite journal}}: Cite journal requires |journal= (help)
  3. 1 2 Hill and Wetherbee (1988), "The structure and taxonomy of Rhinomonas pauca gen. et sp. nov. (Cryptophyceae)", Phycologia, 27 (3): 355–365, doi:10.2216/i0031-8884-27-3-355.1
  4. Pascher, Adolf (1913), Die Süsswasser-Flora: Deutschlands, Österreichs und der Schweiz, vol. 2, pp. 100–103
  5. Butcher (1967), An Introductory Account of the Smaller Algae of British Coastal Waters.
  6. Santore UJ (1982). "Comparative ultrastructure of two members of the Cryptophyceae assigned to the genus Chroomonas — with comments on their taxonomy". Arch. Protistenkd. 125 (1–4): 5–29. doi:10.1016/S0003-9365(82)80002-X.
  7. Santore UJ (1984). "Some aspects of taxonomy in the Cryptophyceae". New Phytol. 98 (4): 627–46. doi: 10.1111/j.1469-8137.1984.tb04153.x .
  8. Santore UJ (1985). "A cytological survey of the genus Cryptomonas (Cryptophyceae) with comments on its taxonomy". Arch. Protistenkd. 130 (1–2): 1–52. doi:10.1016/S0003-9365(85)80031-2.
  9. Santore UJ (1986). "The Ultrastructure of Pyrenomonas heteromorpha comb. nov. (Cryptophyceae)". Botanica Marina. 20 (1): 75–82. doi:10.1515/botm.1986.29.1.75. S2CID   84262672.
  10. Hill, D. R. A. (1991-03-01). "A revised circumscription of Cryptomonas (Cryptophyceae) based on examination of Australian strains". Phycologia. 30 (2): 170–188. doi:10.2216/i0031-8884-30-2-170.1.
  11. Hill D, Wetherbee R (1989). "A reappraisal of the genus Rhodomonas (Cryptophyceae)". Phycologia. 28 (2): 143–158. doi:10.2216/i0031-8884-28-2-143.1.
  12. 1 2 Novarino, G. (2012). "Cryptomonad taxonomy in the 21st century: The first 200 years". Phycological Reports: Current Advances in Algal Taxonomy and Its Applications: Phylogenetic, Ecological and Applied Perspective: 19–52. Retrieved 2018-10-16.
  13. Clay, Brec; Kugrens, Paul; Lee, Robert (October 1999). "A revised classification of Cryptophyta". Botanical Journal of the Linnean Society. 131 (2): 131–151. doi: 10.1111/j.1095-8339.1999.tb01845.x via Oxford Academic.
  14. Deane, et al. (2002), "Cryptomonad Evolution: Nuclear 18S rDNA phylogeny versus cell morphology and pigmentation", Journal of Phycology, 38 (6): 1236–1244, doi:10.1046/j.1529-8817.2002.01250.x, S2CID   51944218
  15. Majaneva, et al. (2014), "Rhinomonas nottbecki n. sp. (Cryptomonadales) and Molecular Phylogeny of the Family Pyrenomonadaceae", Journal of Eukaryotic Microbiology, 61 (5): 480–492, doi:10.1111/jeu.12128, PMID   24913840, S2CID   24145879