Olisthodiscus

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Olisthodiscus
OLISTHODISCUS LUTEUS, ONE OF THE ORGANISMS WHICH CAUSES RED TIDE, PHOTOGRAPHED AT THE ATLANTIC MARINE FISHERIES... - NARA - 555843.tif
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Stramenopiles
Phylum: Gyrista
Subphylum: Ochrophytina
Class: Olisthodiscophyceae
Barcytė, Eikrem & M. Eliáš, 2021 [1]
Order: Olisthodiscales
Cavalier-Smith, 2013 emend. Barcytė, Eikrem & M. Eliáš, 2021
Family: Olisthodiscaceae
Cavalier-Smith, 2013 emend. Barcytė, Eikrem & M. Eliáš, 2021
Genus: Olisthodiscus
Carter 1937 [2]
Type species
Olisthodiscus luteus
Carter 1937
Species

Olisthodiscus is a genus of heterokont algae, present in marine or brackish waters. It is the only genus in the family Olisthodiscaceae, the order Olisthodiscales, and the class Olisthodiscophyceae. After a long history of controversial classifications, in 2021 it was recognized as a phylogenetically distinct lineage from the rest of ochrophyte classes. [1] [3]

Contents

Description

Olisthodiscus is a unicellular organism. Cells are rounded or pear-shaped, flattened and curved somewhat inwards. The cell membrane is covered in scales, fibrils, and bead-shaped protrusions; just underneat the plasma membrane are numerous vesicles. Cells have two flagella: one leads in front of the cell and is somewhat longer than the cell body, while the other trails behind and is equal in length to slightly shorter than the cell body. When swimming, Olisthodiscus glides along a substrate and does not rotate. Multiple plastids are present, and are parietally located; they contain pyrenoids. Olisthodiscus lacks eyespots or contractile vacuoles. However, it has a colored globule which is similar to lipid-storing vacuoles of other species. [1] Olisthodiscus can produce cysts. [1]

Reproduction

Olisthodiscus reproduces asexually by longitudinal fission. It also produces zoospores. Sexual reproduction has not been observed in Olisthodiscus. [1]

Systematics

History of taxonomy

After its description in 1937, Olisthodiscus was placed in Xanthophyceae. [2] In 1985, a study of the ultrastructure of a Japanese strain of Olisthodiscus concluded that it would be more appropriately placed in the Raphidophyceae. [4] However, publications from 1980 to 1992 noted the differences between Olisthodiscus and other raphidophytes, since it lacked ejectile organelles and had a yellowish colour; [5] additionally, it was observed that the flagellar root system was more similar to chrysophytes and brown algae than to raphidophytes. [6] Despite the differences, a revision in 1992 did not accept these arguments and preferred to maintain Olisthodiscus in Raphidophyceae. [7] A thesis from 1999 proposed Olisthodiscophyceae as a separate class for the first time, but it was never published in a peer-reviewed journal. [1]

With the use of molecular phylogenetic analyses, Olisthodiscus appeared as a branch outside Raphidophyceae or any other described ochrophyte class. Because of this, in 2013 it was assigned to a new subclass Sulcophycidae as part of class Hypogyristea, along with pelagophytes and dictyophytes, although with low support for the monophyly of this class. It was proposed that Sulcochrysis belonged to this class along with Olisthodiscus, but due to lack of DNA sequences from this organism it could not be confirmed. [8] In 2021 a study investigated Olisthodiscus and proved it is a separate phylogenetic lineage. It was then placed in its own class, Olisthodiscophyceae. [1]

Ochrophyta
SIII

Bacillariophyceae

Pelagophyceae

Dictyochophyceae

SI

Raphidophyceae

Xanthophyceae

Phaeophyceae

SII

Olisthodiscophyceae

Pinguiophyceae

Limnista

Synchromophyceae

Chrysophyceae

Eustigmatophyceae

Species

Apart from the type species described in 1937, Olisthodiscus luteus , two other species were added in the 20th century: O. carterae and O. magnus , which were later recognized as conspecific with Heterosigma akashiwo and Chattonella marina respectively. This rendered Olisthodiscus monotypic, with O. luteus as its only species, until 2021, when a new species was described: O. tomasii . [1]

Related Research Articles

<span class="mw-page-title-main">Stramenopile</span> Clade of eukaryotes

The Stramenopiles, also called Heterokonts, are a clade of organisms distinguished by the presence of stiff tripartite external hairs. In most species, the hairs are attached to flagella, in some they are attached to other areas of the cellular surface, and in some they have been secondarily lost. Stramenopiles represent one of the three major clades in the SAR supergroup, along with Alveolata and Rhizaria.

<span class="mw-page-title-main">Haptophyte</span> Type of algae

The haptophytes, classified either as the Haptophyta, Haptophytina or Prymnesiophyta, are a clade of algae.

<span class="mw-page-title-main">Synurid</span> Group of algae

The synurids are a small group of heterokont algae, found mostly in freshwater environments, characterized by cells covered in silica scales.

<span class="mw-page-title-main">Brown algae</span> Large group of multicellular algae, comprising the class Phaeophyceae

Brown algae, comprising the class Phaeophyceae, are a large group of multicellular algae, including many seaweeds located in colder waters within the Northern Hemisphere. Brown algae are the major seaweeds of the temperate and polar regions. They are dominant on rocky shores throughout cooler areas of the world. Most brown algae live in marine environments, where they play an important role both as food and as a potential habitat. For instance, Macrocystis, a kelp of the order Laminariales, may reach 60 m (200 ft) in length and forms prominent underwater kelp forests. Kelp forests like these contain a high level of biodiversity. Another example is Sargassum, which creates unique floating mats of seaweed in the tropical waters of the Sargasso Sea that serve as the habitats for many species. Many brown algae, such as members of the order Fucales, commonly grow along rocky seashores. Some members of the class, such as kelps, are used by humans as food.

Phycodnaviridae is a family of large (100–560 kb) double-stranded DNA viruses that infect marine or freshwater eukaryotic algae. Viruses within this family have a similar morphology, with an icosahedral capsid. As of 2014, there were 33 species in this family, divided among 6 genera. This family belongs to a super-group of large viruses known as nucleocytoplasmic large DNA viruses. Evidence was published in 2014 suggesting that specific strains of Phycodnaviridae might infect humans rather than just algal species, as was previously believed. Most genera under this family enter the host cell by cell receptor endocytosis and replicate in the nucleus. Phycodnaviridae play important ecological roles by regulating the growth and productivity of their algal hosts. Algal species such Heterosigma akashiwo and the genus Chrysochromulina can form dense blooms which can be damaging to fisheries, resulting in losses in the aquaculture industry. Heterosigma akashiwo virus (HaV) has been suggested for use as a microbial agent to prevent the recurrence of toxic red tides produced by this algal species. Phycodnaviridae cause death and lysis of freshwater and marine algal species, liberating organic carbon, nitrogen and phosphorus into the water, providing nutrients for the microbial loop.

<span class="mw-page-title-main">Coscinodiscophyceae</span> Class of diatoms

The Coscinodiscophyceae are a class(s) of diatoms. They are similar to the Centrales, a traditional, paraphyletic subdivision of the heterokont algae known as diatoms. The order is named for the shape of the cell walls of centric diatoms, which are circular or ellipsoid in valve view. The valves often bear radially symmetrical ornamental patterns that can appear as dots when viewed with an optical microscope. Some also bear spines on their valves, which may either increase cell surface area and reduce sinking, or act as a deterrent to zooplankton grazers. Unlike pennate diatoms, centric diatoms never have a raphe.

<span class="mw-page-title-main">Raphidophyte</span> Group of aquatic algae

The raphidophytes, formally known as Raphidophycidae or Raphidophyceae, are a small group of eukaryotic algae that includes both marine and freshwater species. All raphidophytes are unicellular, with large cells, but no cell walls. Raphidophytes possess a pair of flagella, organised such that both originate from the same invagination. One flagellum points forwards, and is covered in hair-like mastigonemes, while the other points backwards across the cell surface, lying within a ventral groove. Raphidophytes contain numerous ellipsoid chloroplasts, which contain chlorophylls a, c1 and c2. They also make use of accessory pigments including β-carotene and diadinoxanthin. Unlike other heterokontophytes, raphidophytes do not possess the photoreceptive organelle typical of this group.

<i>Heterosigma akashiwo</i> Species of alga

Heterosigma akashiwo is a species of microscopic algae of the class Raphidophyceae. It is a swimming marine alga that episodically forms toxic surface aggregations known as harmful algal bloom. The species name akashiwo is from the Japanese for "red tide".

<span class="mw-page-title-main">Chlorodendrales</span> Order of algae

Chlorodendrales are an order of green, flagellated, thecate, unicellular eukaryotes, within the green algae class Chlorodendrophyceae. Prasinophyceae are defined by their cellular scales which are composed of carbohydrates, and Chlorodendrales are unique within this group due to these scales forming a fused thecal wall. Cells of Chlorodendrales are completely covered in scales, which fuse around the cell body producing the theca, but remain individually separated on the flagella, of which there are typically four per cell. Species within Chlorodendrales live in both marine and fresh water habitats, occupying both benthic and planktonic food webs. Additionally, they are photoautotrophs, meaning they produce their own food through the conversion of sunlight into chemical energy.

<i>Nephroselmis</i> Genus of algae

Nephroselmis is a genus of green algae. It has been placed in the family Nephroselmidaceae, although a 2009 study suggests that it should be separated into its own class, Nephroselmidophyceae. One species can be an endosymbiont of Hatena arenicola.

<i>Picocystis</i> Genus of algae

Picocystis is a monotypic genus of green algae, the sole species is Picocystis salinarum. It is placed within its own class, Picocystophyceae in the division Chlorophyta.

<span class="mw-page-title-main">Ochrophyte</span> Phylum of algae

Ochrophytes are the photosynthetic stramenopiles, a group of eukaryotes characterized by the presence of two unequal flagella, one of which has tripartite hairs called mastigonemes. In particular, ochrophytes are characterized by their plastids enclosed by four membranes, with thylakoids organized in piles of three, and the presence of chlorophylls a, c, and additional pigments such as β-carotene and xanthophylls. Ochrophytes are one of the most diverse lineages of eukaryotes, containing ecologically important algae such as brown algae and diatoms. They are classified either as phylum Ochrophyta or subphylum Ochrophytina within phylum Gyrista. Their plastid is of red algal origin.

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

Oxyrrhis is a genus of heterotrophic dinoflagellate, the only genus in the family Oxyrrhinaceae. It inhabits a range of marine environments worldwide and is important in the food web dynamics of these ecosystems. It has the potential to be considered a model organism for the study of other protists. Oxyrrhis is an early-branching lineage and has long been described in literature as a monospecific genus, containing only Oxyrrhis marina. Some recent molecular phylogenetic studies argue that Oxyrrhis comprises O. marina and O. maritima as distinct species, while other publications state that the two are genetically diverse lineages of the same species. The genus has previously been suggested to contain O. parasitica as a separate species, however the current consensus appears to exclude this, with Oxyrrhis being monospecific and containing O. marina and O. maritima as separate lineages of the type species. The genus is characterised by its elongated body which is anteriorly prolonged to a point, its complex flagellar apparatuses which attach to the ventral side of the cell, and the unique features of its nucleus.

Pelagomonas is a genus of heterokont algae. It is a monotypic genus and includes a single species, Pelagomonas calceolata which is a unicellular flagellate organism, an ubiquitous constituent of marine picoplankton. It is an ultra-planktonic marine alga.

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

Thaumatomastix is a protist genus of the order Thaumatomonadida, within the phylum Cercozoa and the class Imbricatea. Its species are aquatic, feeding on algae and appearing in waters of a wide range of temperatures and salinities, and are 15-50 micrometers long. They can interchange between flagellated and amoeboid forms, and are notable for being covered in both spiny and flattened siliceous scales.

<i>Gonyostomum semen</i> Species of alga

Gonyostomum semen is a species of freshwater algae in the genus Gonyostomum, with worldwide distribution. They cause nuisance algal blooms and are known to cause allergic reactions to people swimming in lakes.

<span class="mw-page-title-main">Picophagea</span> Class of algae

Picophagea, also known as Synchromophyceae, is a class of photosynthetic stramenopiles. The chloroplast of the Synchromophyceae are surrounded by two membranes and arranged in a way where they share the outer pair of membranes. The entire chloroplast complex is surrounded by an additional two outer membranes.

Lepidodinium is a genus of dinoflagellates belonging to the family Gymnodiniaceae. Lepidodinium is a genus of green dinoflagellates in the family Gymnodiniales. It contains two different species, Lepidodiniumchlorophorum and Lepidodinium viride. They are characterised by their green colour caused by a plastid derived from Pedinophyceae, a green algae group. This plastid has retained chlorophyll a and b, which is significant because it differs from the chlorophyll a and c usually observed in dinoflagellate peridinin plastids. They are the only known dinoflagellate genus to possess plastids derived from green algae. Lepidodinium chlorophorum is known to cause sea blooms, partially off the coast of France, which has dramatic ecological and economic consequences. Lepidodinium produces some of the highest volumes of Transparent Exopolymer Particles of any phytoplankton, which can contribute to bivalve death and the creation of anoxic conditions in blooms, as well as playing an important role in carbon cycling in the ocean. 

<span class="mw-page-title-main">Gyrista</span> Phylum of eukaryotic organisms

Gyrista is a phylum of heterokont protists containing three diverse groups: the mostly photosynthetic Ochrophyta, the parasitic Pseudofungi, and the recently described group of nanoflagellates known as Bigyromonada. Members of this phylum are characterized by the presence of a helix or a double helix/ring system in the ciliary transition region.

Commation is a genus of marine heterotrophic protists closely related to the actinophryids. It contains two species, Commation cryoporinum and Commation eposianum, discovered in antarctic waters and described in 1993. Currently, the genus is classified within a monotypic family Commatiidae and order Commatiida. Along with the photosynthetic raphidophytes, these organisms compose the class of stramenopiles known as Raphidomonadea.

References

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