Cryptomonas | |
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Scientific classification | |
Domain: | Eukaryota |
Clade: | Diaphoretickes |
Phylum: | Cryptista |
Class: | Cryptophyceae |
Order: | Cryptomonadales |
Family: | Cryptomonadaceae |
Genus: | Cryptomonas Ehrenberg, 1831 |
Type species | |
Cryptomonas ovata Ehrenberg 1831 | |
Species | |
See text | |
Synonyms | |
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Cryptomonas is the name-giving genus of the Cryptomonads established by German biologist Christian Gottfried Ehrenberg in 1831. [1] The algae are common in freshwater habitats and brackish water worldwide and often form blooms in greater depths of lakes. [2] The cells are usually brownish or greenish in color and are characteristic of having a slit-like furrow at the anterior. [2] 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. [2] Many species of Cryptomonas can only be identified by DNA sequencing. [3] [4] Cryptomonas can be found in several marine ecosystems in Australia and South Korea. [2] [5]
Cryptomonas has the meaning of hidden small flagellates from “crypto” and “monas”. [6] [7]
Species within Cryptomonas contain four genomes: the nuclear, the nucleomorph, the plastid, and mitochondrial genomes. [3] The plastid genome contains 118 kilobase pairs and is a result of one endosymbiosis event of ancient red alga. [3] The study of genome structures of the genus has contributed to the life-history dependent dimorphism of Cryptomonas, which is discussed in details later in the section Dimorphism.
Cryptomonas are also photolithotrophs that contribute to oxygenic carbon fixation making them greatly critical to the carbon levels of fresh water environments. [4]
Replication of Cryptomonas occurs in early summer when fresh water species are also reproducing. [4] Cryptomonas replicates via mitosis that only takes about ten minutes. [4] Sexual reproduction is not observed in this genus as many other genera of Cryptophytes also do not reproduce sexually. [4]
Organisms are asymmetric with a transparent membrane on the outside. [2] The membrane is not ciliated. [1] Cryptomonas cells are fairly large; they average about 40 micrometers in size and often take the shape of an oval or ovoid. [4] There are two flagella present, yet the two flagella are not equally sized. [1] One is shorter and curled and the other one is longer and straight. [1] The two flagella are fixed to the cell by four unique microtubular roots. [1] [8] In addition, the flagella are lined with small hairs that allow for better movement. [2] There are also contractile vacuoles that control the flow of water in and out. [1]
Two boat-shaped plastids are observed in the cells. [2] In a secondary endosymbiosis event, the phagotrophic ancestor of the Cryptomonas presumably captured a red alga and reduced it to a complex plastid with four envelope membranes. [2] The phycobilisomes of the former red algae were reduced until only phycoerythrin remained. [4] Phycoerythrobilin, a type of red phycobilin pigment, is a chromophore discovered in cyanobacteria, chloroplasts of red algae and some Cryptomonads. [4] Phycoerythrobilin is present in the phycobiliprotein phycoerythrin, the terminal acceptor of energy during the process of photosynthesis. [9] The phycoerythrin was translocated into the thylakoid lumen with its chromophore composition altered; subsequently, phycobiliproteins with at least seven different absorption spectra evolved. [4] Cryptomonas is distinguished by the purple phycoerythrin 566 as an accessory pigment, which gives the organisms a brownish color in appearance. [2]
Cryptomonas are large in size, grow rather slowly, and are limited in nutrients. [4] It also migrates between depths of water in order to reach depths that are ideal for photosynthesis and bacteriograzing, as well avoiding organisms that are their predators. [4] Typically, they are found at depths of up to 102 meters and in a temperature range of -1.4 to 1.5 degrees Celsius. Cryptomonas seem to grow and survive with little competition. [4] Cryptomonas swim actively, and they rotate while moving and sometimes swim in helical motion. [10]
Life history-dependent dimorphism was first described in organisms in 1986. [4] In Proteomonas , another genus of Cryptophyceae, the two morphs revealed large differences in cell size which apparently led to its discovery and subsequent recognition. Cryptomonas has been discovered to be another genus that possesses the characteristic of dimorphism. [4]
Traditionally, Cryptomonas was considered to be 3 separate genera: Chilomonas,Cryptomonas and Campylomonas . [4] Before further molecular analysis, Cryptomonas have been characterized by mainly morphological characters, such as cell size, cell shape, number and color of plastids. However, it was still difficult to define Cryptomonas due to insufficient understanding of morphological characters and less-than adequate visibility of living cells using light microscopy alone to observe the cell structures. Also, laboratories had lacked the condition to detect the different stages of particular organisms. [4]
The furrow-gullet system was used as a standard for organization of genera for many years. [2] Most other Cryptophyte genera have either furrow or gullet, but Cryptomonas is one of the genera that possess a combination of the two, creating a furrow-gullet complex. [2] The furrow-gullet complex is used by the cells to digest food for smaller organisms. [8] Also, ejectisomes are found to be surrounding the complex. [2] Previously, different textures of furrow plates are used to classify genera. For example, a furrow plate (extending posteriorly along one side of the ventral furrow-gullet complex) has been described as “scalariform” in Campylomonas yet “fibrous” in Cryptomonas. [2] In addition, in Cryptomonas, the inner periplast component consists of polygonal plates. In contrast, in Campylomonas, the inner periplast component is a continuous sheet-like layer. [2]
However, during later research, more evidence of both molecular phylogeny and morphology has been found to support the claim that the three genera should be considered one single dimorphic genus. [4] Characters previously used to distinguish Cryptomonas from Campylomonas were found to occur together in dimorphic strains, such as the type of periplast (polygonal periplast plates versus a continuous periplast sheet), indicating that periplast types relate to different life-history stages of a single taxon. [4] To evaluate the taxonomic significance of the type of periplast and other characters previously used to distinguish genera and species, molecular phylogenetic analyses have been used to study two nuclear ribosomal DNA regions (ITS2, partial LSU rDNA) and a nucleomorph ribosomal gene (SSU rDNA). [4] The results of the phylogenetic study provide molecular evidence for a life history-dependent dimorphism in the genus Cryptomonas: the genus Campylomonas represents the alternate morph of Cryptomonas. Campylomonas and Chilomonas are reduced to synonyms of Cryptomonas.
In addition to plastids containing phycoerythrobilin, campylomorphs, formerly genera Campylomonas and Chilomonas, also contain a colorless plastid that lacks photosynthetic pigment: leucoplast. [4]
Since the complete loss of photopigments clearly distinguishes the leukoplastidious cryptophytes from Cryptomonas, the incorporation of “Chilomonas” with Cryptomonas has been highly debatable. Scientists have not yet found out an explanation of how leucoplasts disappear during later life stage and when they disappear. [4]
A flagellate is a cell or organism with one or more whip-like appendages called flagella. The word flagellate also describes a particular construction characteristic of many prokaryotes and eukaryotes and their means of motion. The term presently does not imply any specific relationship or classification of the organisms that possess flagella. However, the term "flagellate" is included in other terms which are more formally characterized.
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. Some may exhibit mixotrophy. They are classified as clade Cryptomonada, which is divided into two classes: heterotrophic Goniomonadea and phototrophic Cryptophyceae. The two groups are united under three shared morphological characteristics: presence of a periplast, ejectisomes with secondary scroll, and mitochondrial cristae with flat tubules. Genetic studies as early as 1994 also supported the hypothesis that Goniomonas was sister to Cryptophyceae. A study in 2018 found strong evidence that the common ancestor of Cryptomonada was an autotrophic protist.
Euglena is a genus of single cell flagellate eukaryotes. It is the best known and most widely studied member of the class Euglenoidea, a diverse group containing some 54 genera and at least 200 species. Species of Euglena are found in fresh water and salt water. They are often abundant in quiet inland waters where they may bloom in numbers sufficient to color the surface of ponds and ditches green (E. viridis) or red (E. sanguinea).
The glaucophytes, also known as glaucocystophytes or glaucocystids, are a small group of unicellular algae found in freshwater and moist terrestrial environments, less common today than they were during the Proterozoic. The stated number of species in the group varies from about 14 to 26. Together with the red algae (Rhodophyta) and the green algae plus land plants, they form the Archaeplastida.
Chromista is a proposed but polyphyletic biological kingdom, refined from the Chromalveolata, consisting of single-celled and multicellular eukaryotic species that share similar features in their photosynthetic organelles (plastids). It includes all eukaryotes whose plastids contain chlorophyll c and are surrounded by four membranes. If the ancestor already possessed chloroplasts derived by endosymbiosis from red algae, all non-photosynthetic Chromista have secondarily lost the ability to photosynthesise. Its members might have arisen independently as separate evolutionary groups from the last eukaryotic common ancestor.
Nucleomorphs are small, vestigial eukaryotic nuclei found between the inner and outer pairs of membranes in certain plastids. They are thought to be vestiges of primitive red and green algal nuclei that were engulfed by a larger eukaryote. Because the nucleomorph lies between two sets of membranes, nucleomorphs support the endosymbiotic theory and are evidence that the plastids containing them are complex plastids. Having two sets of membranes indicate that the plastid, a prokaryote, was engulfed by a eukaryote, an alga, which was then engulfed by another eukaryote, the host cell, making the plastid an example of secondary endosymbiosis.
Phycoerythrin (PE) is a red protein-pigment complex from the light-harvesting phycobiliprotein family, present in cyanobacteria, red algae and cryptophytes, accessory to the main chlorophyll pigments responsible for photosynthesis.The red pigment is due to the prosthetic group, phycoerythrobilin, which gives phycoerythrin its red color.
Yellow-green algae or the Xanthophyceae (xanthophytes) are an important group of heterokont algae. Most live in fresh water, but some are found in marine and soil habitats. They vary from single-celled flagellates to simple colonial and filamentous forms. Xanthophyte chloroplasts contain the photosynthetic pigments chlorophyll a, chlorophyll c, β-carotene, and the carotenoid diadinoxanthin. Unlike other Stramenopiles (heterokonts), their chloroplasts do not contain fucoxanthin, which accounts for their lighter colour. Their storage polysaccharide is chrysolaminarin. Xanthophyte cell walls are produced of cellulose and hemicellulose. They appear to be the closest relatives of the brown algae.
The cryptophyceae are a class of algae, most of which have plastids. About 230 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.
Chlamydomonadaceae is a family of algae within the order Chlamydomonadales. Traditionally, it has been defined as containing single-celled flagellates with a cell wall.
Rhodomonas is a genus of cryptomonads. It is characterized by its red colour, the square-shaped plates of its inner periplast, its short furrow ending in a gullet, and a distinctly shaped chloroplast closely associated with its nucleomorph. Historically, Rhodomonas was characterized by its red chloroplast alone, but this no longer occurs as its taxonomy has become increasingly based on molecular and cellular data. Currently, there is some debate about the taxonomic validity of Rhodomonas as a genus and further research is needed to verify its taxonomic status. Rhodomonas is typically found in marine environments, although freshwater reports exist. It is commonly used as a live feed for various aquaculture species.
Goniomonas is a genus of Cryptomonads and contains five species. It is a genus of single-celled eukaryotes, including both freshwater and marine species. It lacks plastids, which is very unusual among all of the Cryptophyte genera. It may reflect one of only a small number of times that the Cryptophytes evolved into freshwater habitats. Goniomonas seems to have a number of freshwater relatives which have not yet been cultured and named.
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.
Guillardia is a genus of marine biflagellate cryptomonad algae with a plastid obtained through secondary endosymbiosis of a red alga.
Hemiselmis is a genus of cryptomonads.
The kathablepharids are a group of heterotrophic flagellates (Protists) the first species of which was described by Skuja in 1939 as Kathablepharis phoenikoston. His spelling was challenged because of non-compliance with botanical nomenclatural conditions, hence the alternative spelling Katablepharis. As the organism was heterotrophic and usually regarded as 'protozoan', and to favour stability, Skuja's original spelling has largely prevailed. With an anterior pocket and ejectisomes, the kathablepharids were thought initially to be cryptomonads. There were a variety of differences with Cryptomonas and other typical cryptomonads = cryptophytes, such as the thickness, length, and beat pattern of the flagella, their phagotrophic habitat, differences in the ejectisomes, and various features of their ultrastructure. The distinctive characteristics of the group were established from electron microscopical studies by Clay and Kugrens and Vørs. More recently they have been tentatively grouped with the chromalveolates, or distantly with the cryptophytes.
Dinophysis is a genus of dinoflagellates common in tropical, temperate, coastal and oceanic waters. It was first described in 1839 by Christian Gottfried Ehrenberg.
Mesodinium chamaeleon is a ciliate of the genus Mesodinium. It is known for being able to consume and maintain algae endosymbiotically for days before digesting the algae. It has the ability to eat red and green algae, and afterwards using the chlorophyll granules from the algae to generate energy, turning itself from being a heterotroph into an autotroph. The species was discovered in January 2012 outside the coast of Nivå, Denmark by professor Øjvind Moestrup.
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.
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.