| Hyalochlorella | |
|---|---|
Scientific classification  | |
| Clade: | Viridiplantae |
| Division: | Chlorophyta |
| Class: | Trebouxiophyceae |
| Order: | Chlorellales |
| Family: | Oocystaceae |
| Genus: | Hyalochlorella R.O.Poyton, 1970 |
| Species: | H. marina |
| Binomial name | |
| Hyalochlorella marina R.O.Poyton, 1970 | |
Hyalochlorella marina, the only species in the genus Hyalochlorella and also known as Dermocystidium sp., is a marine heterotrophic eukaryote with uncertain phylogenic position. [1] [2]
Hyalochlorella marina was first classified as a fungus under the name Dermocystidium sp. [3] Based morphology and development, it has been classified as a Chlorophyta related to Chlorella but different from the parasite microalgae Prototheca . [1] It also shows similarities to more recently described Ichthyosporea Sphaeroforma species, in particular Sphaeroforma tapetis (previously known as Pseudoperkinsus tapetis). [4] [5] [6] [7] [8]
It is an epiphyte of marine seaweeds but has also been isolated from seawater. Hyalochlorella is found on several shores of east and west coast of the United States, [9] Canada, [10] the United Kingdom, [2] [11] and off the Faroe Islands. [12]
The Apusozoa are a paraphyletic phylum of flagellate eukaryotes. They are usually around 5–20 μm in size, and occur in soils and aquatic habitats, where they feed on bacteria. They are grouped together based on the presence of an organic shell or theca under the dorsal surface of the cell.
Corallochytrium belongs to the class of Corallochytrea within Teretosporea and is a sister group to Ichthyosporea. Corallochytrium limacisporum is the only species of Corallochytrium known so far. It was first discovered and named in the Arabian Sea’s coral lagoons by Kaghu-Kumar in 1987. It was first thought to be a member of the fungi-like thraustochytrids, however, this was later disproven due to Corallochytriums lack of cilia and sagenogenetosome. Little research has been done on the life cycle or morphology. Most research concerning this genus has been done to uncover the evolution of animals and fungi, as Corallochytrium possess both animal and fungal enzymatic trademarks.
Trimastix is a genus of excavate protists, the sole occupant of the order Trimastigida. Trimastix are bacterivorous, free living and anaerobic. It was first observed in 1881 by William Kent. There are few known species, and the genus's role in the ecosystem is largely unknown. However, it is known that they generally live in marine environments within the tissues of decaying organisms to maintain an anoxic environment. Much interest in this group is related to its close association with other members of Preaxostyla. These organisms do not have classical mitochondria, and as such, much of the research involving these microbes is aimed at investigating the evolution of mitochondria.
Leptomyxida is an order of Amoebozoa.
Leptomyxa is a free-living genus of lobose naked multinucleate amoebae in the order Leptomyxida that inhabits freshwater, soil and mosses. It is very closely related to the genus Rhizamoeba, and some species have been moved between the two genera due to molecular data.
Pinaciophora is an amoeboid genus of Heliozoa of uncertain affinity, previously classified as Rhizaria.
Perkinsids are single-celled protists that live as intracellular parasites of a variety of other organisms. They are classified as the class Perkinsea within the monotypic phylum Perkinsozoa. It is part of the eukaryotic supergroup Alveolata, along with dinoflagellates, their closest relatives, and another parasitic group known as Apicomplexa. Perkinsids are found in aquatic environments, as parasites of dinoflagellates and various animals.
Parvilucifera is a genus of marine alveolates that behave as endoparasites of dinoflagellates. It was described in 1999 by biologists Fredrik Norén and Øjvind Moestrup, who identified the genus among collections of Dinophysis dinoflagellates off the coast of Sweden. Initially mistaken for products of sexual reproduction, the round bodies found within these collections were eventually recognized as sporangia, spherical structures that generate zoospores of a parasitic protist. This organism was later identified as P. infectans, the type species. The examination of this organism and its close genetic relationship to Perkinsus led to the creation of the Perkinsozoa phylum within the Alveolata group.
Platysulcus tardus is an eukaryotic microorganism that was recently discovered to be the earliest diverging lineage of the Heterokont phylogenetic tree. It is the only member of the family Platysulcidae, order Platysulcida and class Platysulcea.
Craspedida is an order of choanoflagellate, with members with an exclusively organic covering. Crown group craspedids appeared 422,78 million years ago. Although a previous study from 2017 recovered the divergence of the crown group choanoflagellates (craspedids) at 786.62 million years.
Creolimax fragrantissima is a single-celled protist that occupies a key phylogenetic position to understand the origin of animals. It was isolated from the digestive tract of some marine invertebrates, mainly from the peanut worm, collected from the Northeast Pacific.
Abeoforma whisleri is a single-celled eukaryote that belongs to the Ichthyosporea, a group of protists closely related to animals.
Sphaeroforma arctica, is a unicellular eukaryote with a pivotal position in the tree of life. It was first isolated from the arctic marine amphipod Gammarus setosus. Like other Ichthyosporeans such as Creolimax and Abeoforma, Sphaeroforma arctica are spherical cells characterized with their capacity to grow into multi-nucleated coenocytes. However, a unique feature of S. arctica, is that no obvious budding, hyphal, amoeboid, sporal or flagellated growth stages have been observed in laboratory growth conditions.
Crithidia brevicula is a species of parasitic flagellate protist belonging to the family Trypanosomatidae. It is a monoxenous parasite of insects.
Vampyrella lateritia is a freshwater species of predatory amoebae that feeds on species of algae and is known for its specialized feeding strategy of removing, digesting, and ingesting the cellular contents of its prey. It is the type species of the genus Vampyrella and has been identified in numerous locations around the world including Brazil, Germany, and the eastern United States. Along with Vampyrella pendula, its genome was sequenced in 2012.
Meteora sporadica is a mysterious free-living protozoan discovered in 2002 during sampling at a depth of 1,230 meters below sea level in the Sporades Basin, part of the Mediterranean Sea. So far it is the only species of the genus Meteora.
Rhogostomidae is a family of thecate amoebae with a ventral cleft-like aperture. Their theca is thin and flexible and adheres to the cell. The cleft-like aperture allows them to extend and retract their filose pseudopodia, which they use to move and feed. They are primarily feeding on bacteria, but they are also known to consume yeasts and algae. The family contains three genera: Capsellina, Sacciforma, and Rhogostoma.
An amoeboflagellate is any eukaryotic organism capable of behaving as an amoeba and as a flagellate at some point during their life cycle. Amoeboflagellates present both pseudopodia and at least one flagellum, often simultaneously.
Parviluciferaceae is a family of perkinsozoans, a group of endoparasitic protists present in aquatic environments.
Neometanema is a genus of phagotrophic flagellates belonging to the Euglenida, a diverse group of flagellates in the phylum Euglenozoa. It is the sole genus within the monotypic family Neometanemidae and suborder Metanemina. It composes the order Natomonadida together with a closely related clade of osmotrophs known as Aphagea.
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