The actinophryids are an order of heliozoa, a polyphyletic array of stramenopiles, having a close relationship with pedinellids and Ciliophrys. They are common in fresh water and occasionally found in marine and soil habitats. Actinophryids are unicellular and roughly spherical in shape, with many axopodia that radiate outward from the cell body. Axopodia are a type of pseudopodia that are supported by hundreds of microtubules arranged in interlocking spirals and forming a needle-like internal structure or axoneme. Small granules, extrusomes, that lie under the membrane of the body and axopodia capture flagellates, ciliates and small metazoa that make contact with the arms.
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.
Labyrinthulomycetes (ICBN) or Labyrinthulea (ICZN) is a class of protists that produce a network of filaments or tubes, which serve as tracks for the cells to glide along and absorb nutrients for them. The two main groups are the labyrinthulids and thraustochytrids. They are mostly marine, commonly found as parasites on algae and seagrasses or as decomposers on dead plant material. They also include some parasites of marine invertebrates and mixotrophic species that live in a symbiotic relationship with zoochlorella.
Telonemia is a phylum of microscopic eukaryotes commonly known as telonemids. They are unicellular free-living flagellates with a unique combination of cell structures, including a highly complex cytoskeleton unseen in other eukaryotes.
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.
Ochrophytes, also known as heterokontophytes or stramenochromes, are a group of algae. They are the photosynthetic stramenopiles, a group of eukaryotes, organisms with a cell nucleus, characterized by the presence of two unequal flagella, one of which has tripartite hairs called mastigonemes. In particular, they are characterized by photosynthetic organelles or plastids enclosed by four membranes, with membrane-bound compartments called thylakoids organized in piles of three, chlorophyll a and c as their photosynthetic pigments, 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 Heterokontophyta, or as subphylum Ochrophytina within phylum Gyrista. Their plastids are of red algal origin.
Bigyra is a phylum of microscopic eukaryotes that are found at the base of the Stramenopiles clade. It includes three well-known heterotrophic groups Bicosoecida, Opalinata and Labyrinthulomycetes, as well as several small clades initially discovered through environmental DNA samples: Nanomonadea, Placididea, Opalomonadea and Eogyrea. The classification of Bigyra has changed several times since its origin, and its monophyly remains unresolved.
Opalozoa is a subphylum of heterotrophic protists of the phylum Bigyra, and is the sister group to Sagenista. Opalozoans are non-photosynthetic heterokonts that are ancestrally phagotrophic but many times have evolved to be osmotrophic saprotrophs in the gut of vertebrate 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.
Kiitoksia is a genus of aquatic protist. The taxonomic position of the genus is still uncertain and it has not found a robust location in any subgroup.
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.
Raphidomonadea is a class of Stramenopiles containing both photosynthetic and phagotrophic protists. The phagotrophic groups are known as Raphopoda, and comprise actinophryid heliozoa and the marine genus Commation. The photosynthetic groups are known as the raphidophyte algae. Their relationship was elucidated through phylogenetic analyses.
Tetrahelia is a genus of four-ciliated protists belonging to the Endohelea, a group of heterotrophic eukaryotes previously considered heliozoa. It is the only genus in the family Tetraheliidae and order Axomonadida. It is a monotypic genus, containing the sole species Tetrahelia pterbica, previously classified as Tetradimorpha.
Minimassisteria is a marine bacterivorous genus of protists with only one species, M. diva, that presents three different lifestyle forms. It has a widespread geographic distribution. It is an amoeboflagellate most closely related to Massisteria, and together comprise the family Massisteriidae.
Thecamonadinae is a subfamily of heterotrophic protists. It is a monophyletic group, or clade, of apusomonads, a group of protozoa with two flagella closely related to the eukaryotic supergroup Opisthokonta. The subfamily contains two genera Chelonemonas and Thecamonas, which are found in marine habitats.
Heliorapha is a genus of heliozoan protists, amoeboid eukaryotes with stiff axopodia radiating from their cells. It contains one species, Heliorapha azurina. It is classified within a monotypic family Helioraphidae inside the actinophryids, a group of heliozoa that belong to the Ochrophyta along with other protists such as diatoms and brown algae.
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.
Commation eposianum is a species of heterotrophic protists discovered in 1993 in Antarctic waters. It is one of two species in the Commatiida, an order of stramenopiles closely related to actinophryids, a group of heliozoan protists, and to raphidophytes, a group of algae.
Raphopoda is a grouping of heterotrophic protists. It contains the heterotroph organisms within class Raphidomonadea, classified as two orders: Commatiida, comprised by the sole genus of flagellates Commation, and Actinophryida, an order of heliozoa, amoebae with stiff specialized pseudopodia called axopodia.
Colponemids are free-living alveolates, unicellular flagellates related to dinoflagellates, apicomplexans and ciliates. They are predators of other small eukaryotes, found in freshwater, marine and soil environments. They do not form a solid clade, but a sparse group of deep-branching alveolate lineages.
