Diatom

Diatoms are protists that form massive annual spring and fall blooms in aquatic environments and are estimated to be responsible for about half of photosynthesis in the global oceans. This predictable annual bloom dynamic fuels higher trophic levels and initiates delivery of carbon into the deep ocean biome. Diatoms have complex life history strategies that are presumed to have contributed to their rapid genetic diversification into ~200,000 species that are distributed between the two major diatom groups: centrics and pennates. ==Morphology==

File:3D-animation of the diatom Corethron sp.ogg|thumb|upright=1.8| (a) Green: [DiOC6(3) fluorescence] - stains cellular membranes indicating the core cell bodies(b) Cyan: [PLL-A546 fluorescence] - generic counterstain for visualising eukaryotic cell surfaces(c) Blue: [Hoechst fluorescence] - stains DNA, identifies nuclei(d) Red: [chlorophyll autofluorescence] - resolves chloroplasts Diatoms are generally 20 to 200 micrometers in size, with a few larger species. Their yellowish-brown chloroplasts, the site of photosynthesis, are typical of heterokonts, having four cell membranes and containing pigments such as the carotenoid fucoxanthin. Individuals usually lack flagella, but they are present in male gametes of the centric diatoms and have the usual heterokont structure, including the hairs (mastigonemes) characteristic in other groups. Diatoms are often referred as "jewels of the sea" or "living opals" due to their optical properties. The biological function of this structural coloration is not clear, but it is speculated that it may be related to communication, camouflage, thermal exchange and/or UV protection. Diatoms build intricate hard but porous cell walls called frustules composed primarily of silica. can be highly patterned with a variety of pores, ribs, minute spines, marginal ridges and elevations; all of which can be used to delineate genera and species. The cell itself consists of two halves, each containing an essentially flat plate, or valve, and marginal connecting, or girdle band. One half, the hypotheca, is slightly smaller than the other half, the epitheca. Diatom morphology varies. Although the shape of the cell is typically circular, some cells may be triangular, square, or elliptical. Their distinguishing feature is a hard mineral shell or frustule composed of opal (hydrated, polymerized silicic acid). Diatoms are divided into two groups that are distinguished by the shape of the frustule: the centric diatoms and the pennate diatoms. Pennate diatoms are bilaterally symmetric. Each one of their valves have openings that are slits along the raphes and their shells are typically elongated parallel to these raphes. They generate cell movement through cytoplasm that streams along the raphes, always moving along solid surfaces. Centric diatoms are radially symmetric. They are composed of upper and lower valves – epitheca and hypotheca – each consisting of a valve and a girdle band that can easily slide underneath each other and expand to increase cell content over the diatoms progression. The cytoplasm of the centric diatom is located along the inner surface of the shell and provides a hollow lining around the large vacuole located in the center of the cell. This large, central vacuole is filled by a fluid known as "cell sap" which is similar to seawater but varies with specific ion content. The cytoplasmic layer is home to several organelles, like the chloroplasts and mitochondria. Before the centric diatom begins to expand, its nucleus is at the center of one of the valves and begins to move towards the center of the cytoplasmic layer before division is complete. Centric diatoms have a variety of shapes and sizes, depending on from which axis the shell extends, and if spines are present. 's 1904 (Art Forms of Nature), showing pennate (left) and centric (right) frustules. ==Silicification==

Diatom cells are contained within a unique silica cell wall known as a frustule made up of two valves called thecae, that typically overlap one another. The biogenic silica composing the cell wall is synthesised intracellularly by the polymerisation of silicic acid monomers. This material is then extruded to the cell exterior and added to the wall. In most species, when a diatom divides to produce two daughter cells, each cell keeps one of the two valves and grows a smaller valve within it. As a result, after each division cycle, the average size of diatom cells in the population gets smaller. Once such cells reach a certain minimum size, rather than simply divide, they reverse this decline by forming an auxospore, usually through meiosis and sexual reproduction, but exceptions exist. The auxospore expands in size to give rise to a much larger cell, which then returns to size-diminishing divisions. from an Arctic meltpond, infected with two chytrid-like [zoo-]sporangium fungal pathogens (in false-colour red). Scale bar = 10 μm. The exact mechanism of transferring silica absorbed by the diatom to the cell wall is unknown. Much of the sequencing of diatom genes comes from the search for the mechanism of silica uptake and deposition in nano-scale patterns in the frustule. The most success in this area has come from two species, Thalassiosira pseudonana, which has become the model species, as the whole genome was sequenced and methods for genetic control were established, and Cylindrotheca fusiformis, in which the important silica deposition proteins silaffins were first discovered. Silaffins, sets of polycationic peptides, were found in C. fusiformis cell walls and can generate intricate silica structures. These structures demonstrated pores of sizes characteristic to diatom patterns. When T. pseudonana underwent genome analysis it was found that it encoded a urea cycle, including a higher number of polyamines than most genomes, as well as three distinct silica transport genes. In a phylogenetic study on silica transport genes from 8 diverse groups of diatoms, silica transport was found to generally group with species. These two protein structures have been shown to create sheets of patterned silica in-vivo with irregular pores on the scale of diatom frustules. One hypothesis as to how these proteins work to create complex structure is that residues are conserved within the SDV's, which is unfortunately difficult to identify or observe due to the limited number of diverse sequences available. Though the exact mechanism of the highly uniform deposition of silica is as yet unknown, the Thalassiosira pseudonana genes linked to silaffins are being looked to as targets for genetic control of nanoscale silica deposition. The ability of diatoms to make silica-based cell walls has been the subject of fascination for centuries. It started with a microscopic observation by an anonymous English country nobleman in 1703, who observed an object that looked like a chain of regular parallelograms and debated whether it was just crystals of salt, or a plant. The viewer decided that it was a plant because the parallelograms didn't separate upon agitation, nor did they vary in appearance when dried or subjected to warm water (in an attempt to dissolve the "salt"). Unknowingly, the viewer's confusion captured the essence of diatoms—mineral utilizing plants. It is not clear when it was determined that diatom cell walls are made of silica, but in 1939 a seminal reference characterized the material as silicic acid in a "subcolloidal" state Identification of the main chemical component of the cell wall spurred investigations into how it was made. These investigations have involved, and been propelled by, diverse approaches including, microscopy, chemistry, biochemistry, material characterisation, molecular biology, 'omics, and transgenic approaches. The results from this work have given a better understanding of cell wall formation processes, establishing fundamental knowledge which can be used to create models that contextualise current findings and clarify how the process works. The process of building a mineral-based cell wall inside the cell, then exporting it outside, is a massive event that must involve large numbers of genes and their protein products. The act of building and exocytosing this large structural object in a short time period, synched with cell cycle progression, necessitates substantial physical movements within the cell as well as dedication of a significant proportion of the cell's biosynthetic capacities. These were followed by insights into how higher order assembly of silica structures might occur. More recent reports describe the identification of novel components involved in higher order processes, the dynamics documented through real-time imaging, and the genetic manipulation of silica structure. The approaches established in these recent works provide practical avenues to not only identify the components involved in silica cell wall formation but to elucidate their interactions and spatio-temporal dynamics. This type of holistic understanding will be necessary to achieve a more complete understanding of cell wall synthesis. ==Behaviour==

Most centric and araphid pennate diatoms are nonmotile, and their relatively dense cell walls cause them to readily sink. Planktonic forms in open water usually rely on turbulent mixing of the upper layers of the oceanic waters by the wind to keep them suspended in sunlit surface waters. Many planktonic diatoms have also evolved features that slow their sinking rate, such as spines or the ability to grow in colonial chains. These adaptations increase their surface area to volume ratio and drag, allowing them to stay suspended in the water column longer. Individual cells may regulate buoyancy via an ionic pump. Some pennate diatoms are capable of a type of locomotion called "gliding", which allows them to move across surfaces via adhesive mucilage secreted through a seamlike structure called the raphe. In order for a diatom cell to glide, it must have a solid substrate for the mucilage to adhere to. Cells are solitary or united into colonies of various kinds, which may be linked by siliceous structures; mucilage pads, stalks or tubes; amorphous masses of mucilage; or by threads of chitin (polysaccharide), which are secreted through strutted processes of the cell. sp. (56–62), Asteromphalus sp. (63), Aulacoseira sp. (64–66), and Chaetoceros'' (see twin image above) often grow in chains, and have features such as spines which slow sinking rates by increasing drag. diatoms form chain-like colonies, like these collected near the Antarctic peninsula coast by the schooner of the Tara'' Oceans Expedition for plankton research.This projection of a stack of confocal images shows the diatoms' cell wall (cyan), chloroplasts (red), DNA (blue), membranes and organelles (green). Phytochromes Even though light is a crucial part of how diatoms create oxygen for the planet, the organism faces some difficulties when it comes to detecting its energy source. The intensity of light in water lessens as depth increases. Light penetration also greatly differs between coastal and open waters and during the changing seasons. Such factors result in a less efficient photosynthetic conversion, similar to the process of plant photosynthesis, as the light becomes dimmer, photosynthesis slows down. However, diatoms possess photoreceptors, which are light-activated proteins, that aid them in sensing different light wavelengths, such as red light and far-red light, for detecting light in the ocean. It has been demonstrated that diatoms use photoreceptors called phytochromes to determine the water's depth to respond to light signals. Phytochromes can sense red and far-red light and are widely known to be found in both plants and phytoplankton. These proteins switch between two states called red-light and far red-light so that the organism can detect and respond to any changes in the perceived underwater light intensity and spectrum. Since red and far-red light is known to diminish with increasing water depth, many questioned the importance of the phytochromes' role when it comes to marine life. Analysis of environmental DNA sequences taken from the Tara Oceans expedition, as well as the genome data from cultured diatoms which demonstrated that the phytochrome-encoding genes were mostly found in diatoms living in temperate and polar regions in mid-to-high latitudes Removal of the phytochrome gene from the diatom Thalassiosira pseudonana grown in a similar deep-water simulation demonstrated that the mutant diatom had a lower photosynthetic efficiency, as well as a reduced photoprotection, compared to the wild-type diatoms with the phytochrome gene, They suggest that the diatom phytochromes went through an evolutionary adaptation to acclimate to the violent waters in the open waters of the temperate and polar regions. Since the function of diatom phytochromes is to sense the water depth, it provides the diatoms information that is very advantageous in regions with differing seasons. These photoreceptors play a critical role in helping phytoplankton adjust to environments with limited light, specifically the deep-water environments. == Life cycle ==

Reproduction and cell size Reproduction among these organisms is asexual by binary fission, during which the diatom divides into two parts, producing two "new" diatoms with identical genes. Each new organism receives one of the two frustules – one larger, the other smaller – possessed by the parent, which is now called the epitheca; and is used to construct a second, smaller frustule, the hypotheca. The diatom that received the larger frustule becomes the same size as its parent, but the diatom that received the smaller frustule remains smaller than its parent. This causes the average cell size of this diatom population to decrease. Nonetheless, in order to restore the cell size of a diatom population for those that do endure size reduction, sexual reproduction and auxospore formation must occur. The entire lifecycles of only a few diatoms have been described and rarely have sexual events been captured in the environment. Sexual reproduction involves production of gametes and the fusion of gametes to form a zygote in which maximal cell size is restored. An exploration of the genomes of five diatoms and one diatom transcriptome led to the identification of 42 genes potentially involved in meiosis. Thus a meiotic toolkit appears to be conserved in these six diatom species, == Ecology ==

Distribution Diatoms are a widespread group and can be found in the oceans, in fresh water, in soils, and on damp surfaces. They are one of the dominant components of phytoplankton in nutrient-rich coastal waters and during oceanic spring blooms, since they can divide more rapidly than other groups of phytoplankton. However, a more recent 2016 study estimates that the number is closer to 20%. Spatial distribution of marine phytoplankton species is restricted both horizontally and vertically. Growth Planktonic diatoms in freshwater and marine environments typically exhibit a "boom and bust" (or "bloom and bust") lifestyle. When conditions in the upper mixed layer (nutrients and light) are favourable (as at the spring), their competitive edge and rapid growth rate enables them to dominate phytoplankton communities ("boom" or "bloom"). As such they are often classed as opportunistic r-strategists (i.e. those organisms whose ecology is defined by a high growth rate, r). Impact The freshwater diatom Didymosphenia geminata, commonly known as Didymo, causes severe environmental degradation in water-courses where it blooms, producing large quantities of a brown jelly-like material called "brown snot" or "rock snot". This diatom is native to Europe and is an invasive species both in the antipodes and in parts of North America. The problem is most frequently recorded from Australia and New Zealand. When conditions turn unfavourable, usually upon depletion of nutrients, diatom cells typically increase in sinking rate and exit the upper mixed layer ("bust"). This sinking is induced by either a loss of buoyancy control, the synthesis of mucilage that sticks diatoms cells together, or the production of heavy resting spores. Sinking out of the upper mixed layer removes diatoms from conditions unfavourable to growth, including grazer populations and higher temperatures (which would otherwise increase cell metabolism). Cells reaching deeper water or the shallow seafloor can then rest until conditions become more favourable again. In the open ocean, many sinking cells are lost to the deep, but refuge populations can persist near the thermocline. Ultimately, diatom cells in these resting populations re-enter the upper mixed layer when vertical mixing entrains them. In most circumstances, this mixing also replenishes nutrients in the upper mixed layer, setting the scene for the next round of diatom blooms. In the open ocean (away from areas of continuous upwelling), this cycle of bloom, bust, then return to pre-bloom conditions typically occurs over an annual cycle, with diatoms only being prevalent during the spring and early summer. In some locations, however, an autumn bloom may occur, caused by the breakdown of summer stratification and the entrainment of nutrients while light levels are still sufficient for growth. Since vertical mixing is increasing, and light levels are falling as winter approaches, these blooms are smaller and shorter-lived than their spring equivalents. In the open ocean, the diatom (spring) bloom is typically ended by a shortage of silicon. Unlike other minerals, the requirement for silicon is unique to diatoms and it is not regenerated in the plankton ecosystem as efficiently as, for instance, nitrogen or phosphorus nutrients. This can be seen in maps of surface nutrient concentrations – as nutrients decline along gradients, silicon is usually the first to be exhausted (followed normally by nitrogen then phosphorus). Because of this bloom-and-bust cycle, diatoms are believed to play a disproportionately important role in the export of carbon from oceanic surface waters (see also the biological pump). Significantly, they also play a key role in the regulation of the biogeochemical cycle of silicon in the modern ocean. noted that, relative to organic cell walls, silica frustules require less energy to synthesize (approximately 8% of a comparable organic wall), potentially a significant saving on the overall cell energy budget. In a now classic study, Egge and Aksnes (1992) have suggested that the biogenic silica in diatom cell walls acts as an effective pH buffering agent, facilitating the conversion of bicarbonate to dissolved CO2 (which is more readily assimilated). More generally, whether or not by reason of these possible advantages conferred by their use of silicon, diatoms typically have higher growth rates than other algae of the same corresponding size. Marine diatoms can be collected by direct water sampling, and benthic forms can be secured by scraping barnacles, oyster and other shells. Diatoms are frequently present as a brown, slippery coating on submerged stones and sticks, and may be seen to "stream" with river current. The surface mud of a pond, ditch, or lagoon will almost always yield some diatoms. Living diatoms are often found clinging in great numbers to filamentous algae, or forming gelatinous masses on various submerged plants. Cladophora is frequently covered with Cocconeis, an elliptically shaped diatom; Vaucheria is often covered with small forms. Since diatoms form an important part of the food of molluscs, tunicates, and fishes, the alimentary tracts of these animals often yield forms that are not easily secured in other ways. Diatoms can be made to emerge by filling a jar with water and mud, wrapping it in black paper and letting direct sunlight fall on the surface of the water. Within a day, the diatoms will come to the top in a scum and can be isolated. ==Biogeochemistry==

File:Oceanic Silicon Cycle Budget.svg|The modern oceanic silicon cycleFluxes are in Tmol Si y−1 (1 Tmol = 28 million metric tons of silicon) Silica cycle The diagram shows the major fluxes of silicon in the current ocean. Most biogenic silica in the ocean (silica produced by biological activity) comes from diatoms. Diatoms extract dissolved silicic acid from surface waters as they grow, and return it to the water column when they die. Inputs of silicon arrive from above via aeolian dust, from the coasts via rivers, and from below via seafloor sediment recycling, weathering, and hydrothermal activity. Although diatoms may have existed since the Triassic, the timing of their ascendancy and "take-over" of the silicon cycle occurred more recently. Prior to the Phanerozoic (before 544 Ma), it is believed that microbial or inorganic processes weakly regulated the ocean's silicon cycle. Subsequently, the cycle appears dominated (and more strongly regulated) by the radiolarians and siliceous sponges, the former as zooplankton, the latter as sedentary filter-feeders primarily on the continental shelves. Within the last 100 My, it is thought that the silicon cycle has come under even tighter control, and that this derives from the ecological ascendancy of the diatoms. However, the precise timing of the "take-over" remains unclear, and different authors have conflicting interpretations of the fossil record. Some evidence, such as the displacement of siliceous sponges from the shelves, suggests that this takeover began in the Cretaceous (146 Ma to 66 Ma), while evidence from radiolarians suggests "take-over" did not begin until the Cenozoic (66 Ma to present). File:Ocean carbon cycle and diatom carbon dioxide concentration mechanisms 2.jpg|alt=Ocean carbon cycle and diatom carbon dioxide concentration mechanisms|Ocean carbon cycle and diatom carbon dioxide concentration mechanisms Carbon cycle The diagram depicts some mechanisms by which marine diatoms contribute to the biological carbon pump and influence the ocean carbon cycle. The anthropogenic CO2 emission to the atmosphere (mainly generated by fossil fuel burning and deforestation) is nearly 11 gigatonne carbon (GtC) per year, of which almost 2.5 GtC is taken up by the surface ocean. In surface seawater (pH 8.1–8.4), bicarbonate () and carbonate ions () constitute nearly 90 and 2 (CO2 aqueous) contributes 2 in the ocean and its slow diffusion rate in water, diatoms fix 10–20 GtC annually via photosynthesis thanks to their carbon dioxide concentrating mechanisms, allowing them to sustain marine food chains. In addition, 0.1–1% of this organic material produced in the euphotic layer sinks down as particles, thus transferring the surface carbon toward the deep ocean and sequestering atmospheric CO2 for thousands of years or longer. The remaining organic matter is remineralized through respiration. Thus, diatoms are one of the main players in this biological carbon pump, which is arguably the most important biological mechanism in the Earth System allowing CO2 to be removed from the carbon cycle for very long period. Urea cycle A feature of diatoms is the urea cycle, which is a feature shared with animals. In 2011, Allen et al. established that diatoms have a functioning urea cycle. This result was significant, since prior to this, the urea cycle was thought to have originated with the metazoans, which appeared several hundreds of millions of years before the diatoms. Their study demonstrated that while diatoms and animals use the urea cycle for different ends, they are seen to share this feature that more closely related organisms such as plants lack. While often overlooked in photosynthetic organisms, the mitochondria also play critical roles in energy balance. Two nitrogen-related pathways are relevant and they may also change under ammonium () nutrition compared with nitrate () nutrition. First, in diatoms, and likely some other algae, there is a urea cycle. The long-known function of the urea cycle in animals is to excrete excess nitrogen produced by amino acid Catabolism; like photorespiration, the urea cycle had long been considered a waste pathway. However, in diatoms the urea cycle appears to play a role in exchange of nutrients between the mitochondria and the cytoplasm, and potentially the plastid and may help to regulate ammonium metabolism. Photosynthetic diatoms that find themselves in an environment absent of oxygen and/or sunlight can switch to anaerobic respiration known as nitrate respiration (DNRA), and stay dormant for up till months and decades. Major pigments of diatoms are chlorophylls a and c, beta-carotene, fucoxanthin, diatoxanthin and diadinoxanthin. ==Taxonomy==

Diatoms belong to a large group of protists, many of which contain plastids rich in chlorophylls a and c. The group has been variously referred to as heterokonts, chrysophytes, chromists or stramenopiles. Many are autotrophs such as golden algae and kelp; and heterotrophs such as water moulds, opalinids, and actinophryid heliozoa. The classification of this area of protists is still unsettled. In terms of rank, they have been treated as a division, phylum, kingdom, or something intermediate to those. Consequently, diatoms are ranked anywhere from a class, usually called Diatomophyceae or Bacillariophyceae, to a division (=phylum), usually called Bacillariophyta, with corresponding changes in the ranks of their subgroups. Genera and species An estimated 20,000 extant diatom species are believed to exist, of which around 12,000 have been named to date according to Guiry, 2012 (other sources give a wider range of estimates). Around 1,000–1,300 diatom genera have been described, both extant and fossil, of which some 250–300 exist only as fossils. Classes and orders For many years the diatoms—treated either as a class (Bacillariophyceae) or a phylum (Bacillariophyta)—were divided into just 2 orders, corresponding to the centric and the pennate diatoms (Centrales and Pennales). This classification was extensively overhauled by Round, Crawford and Mann in 1990 who treated the diatoms at a higher rank (division, corresponding to phylum in zoological classification), and promoted the major classification units to classes, maintaining the centric diatoms as a single class Coscinodiscophyceae, but splitting the former pennate diatoms into 2 separate classes, Fragilariophyceae and Bacillariophyceae (the latter older name retained but with an emended definition), between them encompassing 45 orders, the majority of them new. As of 2020, it is recognised that the 1990 system of Round et al. is in need of revision with the advent of newer molecular work, however the best system to replace it is unclear. Current systems in widespread use, such as AlgaeBase, the World Register of Marine Species, and its contributing database DiatomBase, and the system for "all life" represented in Ruggiero et al., 2015, all retain the Round et al. treatment as their basis, albeit with diatoms as a whole treated as a class rather than division/phylum, with Round et al.'s classes reduced to subclasses, for better agreement with the treatment of phylogenetically adjacent groups and their containing taxa. (For references refer the individual sections below). One proposal, by Linda Medlin and co-workers commencing in 2004, considers some of the centric diatoms more closely related to the pennates to be split off as a new class, Mediophyceae, itself more closely aligned with the pennate diatoms than the remaining centrics. This hypothesis—later designated the Coscinodiscophyceae-Mediophyceae-Bacillariophyceae, or Coscinodiscophyceae+(Mediophyceae+Bacillariophyceae) (CMB) hypothesis—has been accepted by D.G. Mann among others, who use it as the basis for the classification of diatoms as presented in Adl. et al.'s series of syntheses (2005, 2012, 2019), and also in the Bacillariophyta chapter of the 2017 Handbook of the Protists edited by Archibald et al., with some modifications reflecting the apparent non-monophyly of Medlin et al. original "Coscinodiscophyceae". Meanwhile, a group led by E.C. Theriot favours a different hypothesis of phylogeny, which has been termed the structural gradation hypothesis (SGH) and does not recognise the Mediophyceae as a monophyletic group. Another analysis, by Parks et al., 2018, finds that the radial centric diatoms (Medlin et al.'s Coscinodiscophyceae) are not monophyletic, but supports the monophyly of Mediophyceae minus Attheya, which is an anomalous genus. Discussion of the relative merits of these conflicting schemes continues by the various parties involved. Adl et al., 2019 treatment In 2019, Adl et al. presented the following classification of diatoms, while noting: "This revision reflects numerous advances in the phylogeny of the diatoms over the last decade. Due to our poor taxon sampling outside of the Mediophyceae and pennate diatoms, and the known and anticipated diversity of all diatoms, many clades appear at a high classification level (and the higher level classification is rather flat)." This classification accepts the Mediophyceae of Medlin and co-workers and introduces new clades for a number of otherwise isolated genera. • Ochrophyta Cavalier-Smith 1986, emend. Cavalier-Smith & Chao 1996 (ochrophytes) • Diatomista Derelle et al. 2016, emend. Cavalier-Smith 2017 (diatoms plus a subset of other ochrophyte groups) • Diatomeae Dumortier 1821 [= Bacillariophyta Haeckel 1878] (diatoms) • Leptocylindrophytina D.G. Mann in Adl et al. 2019 • Leptocylindrophyceae D.G. Mann in Adl et al. 2019 (Leptocylindrus, Tenuicylindrus) • Corethrophyceae D.G. Mann in Adl et al. 2019 (Corethron) • Ellerbeckiophytina D.G. Mann in Adl et al. 2019 (Ellerbeckia) • Probosciophytina D.G. Mann in Adl et al. 2019 (Proboscia) • Melosirophytina D.G. Mann in Adl et al. 2019 (Aulacoseira, Melosira, Hyalodiscus, Stephanopyxis, Paralia, Endictya) • Coscinodiscophytina Medlin & Kaczmarska 2004, emend. (Actinoptychus, Coscinodiscus, Actinocyclus, Asteromphalus, Aulacodiscus, Stellarima) • Rhizosoleniophytina D.G. Mann in Adl et al. 2019 (Guinardia, Rhizosolenia, Pseudosolenia) • Arachnoidiscophytina D.G. Mann in Adl et al. 2019 (Arachnoidiscus) • Bacillariophytina Medlin & Kaczmarska 2004, emend. • Mediophyceae Jouse & Proshkina-Lavrenko in Medlin & Kaczmarska 2004 • Chaetocerotophycidae Round & R.M. Crawford in Round et al. 1990, emend. • Lithodesmiophycidae Round & R.M. Crawford in Round et al. 1990, emend. • Thalassiosirophycidae Round & R.M. Crawford in Round et al. 1990 • Cymatosirophycidae Round & R.M. Crawford in Round et al. 1990 • Odontellophycidae D.G. Mann in Adl et al. 2019 • Chrysanthemodiscophycidae D.G. Mann in Adl et al. 2019 • Biddulphiophyceae D.G. Mann in Adl et al. 2019 • Biddulphiophycidae Round and R.M. Crawford in Round et al. 1990, emend. • Attheya • Bacillariophyceae Haeckel 1878, emend. • Striatellaceae • Urneidophycidae Medlin 2016 • Fragilariophycidae Round in Round, Crawford & Mann 1990, emend. • Bacillariophycidae D.G. Mann in Round, Crawford & Mann 1990, emend. See taxonomy of diatoms for more details. == Evolution and fossil record ==

Origin Heterokont chloroplasts appear to derive from those of red algae, rather than directly from prokaryotes as occurred in plants. This suggests they had a more recent origin than many other algae. However, fossil evidence is scant, and only with the evolution of the diatoms themselves do the heterokonts make a serious impression on the fossil record. Earliest fossils The earliest known fossil diatoms date from the early Jurassic (~185 Ma ago), although the molecular clock evidence suggests an earlier origin. It has been suggested that their origin may be related to the end-Permian mass extinction (~250 Ma), after which many marine niches were opened. The gap between this event and the time that fossil diatoms first appear may indicate a period when diatoms were unsilicified and their evolution was cryptic. Since the advent of silicification, diatoms have made a significant impression on the fossil record, with major fossil deposits found as far back as the early Cretaceous, and with some rocks such as diatomaceous earth, being composed almost entirely of them. Relation to grasslands The expansion of grassland biomes and the evolutionary radiation of grasses during the Miocene is believed to have increased the flux of soluble silicon to the oceans, and it has been argued that this promoted the diatoms during the Cenozoic era. Recent work suggests that diatom success is decoupled from the evolution of grasses, although both diatom and grassland diversity increased strongly from the middle Miocene. Relation to climate Diatom diversity over the Cenozoic has been very sensitive to global temperature, particularly to the equator-pole temperature gradient. Warmer oceans, particularly warmer polar regions, have in the past been shown to have had substantially lower diatom diversity. Future warm oceans with enhanced polar warming, as projected in global-warming scenarios, could thus in theory result in a significant loss of diatom diversity, although from current knowledge it is impossible to say if this would occur rapidly or only over many tens of thousands of years. Where diatom biozones are well established and calibrated to the geomagnetic polarity time scale (e.g., Southern Ocean, North Pacific, eastern equatorial Pacific), diatom-based age estimates may be resolved to within diatom, δ18Odiatom, and δ30Sidiatom). In 2015, Swann and Snelling used these isotope records to document historic changes in the photic zone conditions of the north-west Pacific Ocean, including nutrient supply and the efficiency of the soft-tissue biological pump, from the modern day back to marine isotope stage 5e, which coincides with the last interglacial period. Peaks in opal productivity in the marine isotope stage are associated with the breakdown of the regional halocline stratification and increased nutrient supply to the photic zone. File:Ocean changes from the last interglacial to the modern day A.png File:Ocean changes from the last interglacial to the modern day B.png The initial development of the halocline and stratified water column has been attributed to the onset of major Northern Hemisphere glaciation at 2.73 Ma, which increased the flux of freshwater to the region, via increased monsoonal rainfall and/or glacial meltwater, and sea surface temperatures. The decrease of abyssal water upwelling associated with this may have contributed to the establishment of globally cooler conditions and the expansion of glaciers across the Northern Hemisphere from 2.73 Ma. other studies have shown that the stratification boundary may have broken down in the late Quaternary at glacial terminations and during the early part of interglacials. Turnover Although no mass extinctions of marine diatoms have been observed during the Cenozoic, times of relatively rapid evolutionary turnover in marine diatom species assemblages occurred near the Paleocene–Eocene boundary, and at the Eocene–Oligocene boundary. Further turnover of assemblages took place at various times between the middle Miocene and late Pliocene, in response to progressive cooling of polar regions and the development of more endemic diatom assemblages. A global trend toward more delicate diatom frustules has been noted from the Oligocene to the Quaternary. This coincides with an increasingly more vigorous circulation of the ocean's surface and deep waters brought about by increasing latitudinal thermal gradients at the onset of major ice sheet expansion on Antarctica and progressive cooling through the Neogene and Quaternary towards a bipolar glaciated world. This caused diatoms to take in less silica for the formation of their frustules. Increased mixing of the oceans renews silica and other nutrients necessary for diatom growth in surface waters, especially in regions of coastal and oceanic upwelling. ==Genetics==

Expressed sequence tagging In 2002, the first insights into the properties of the Phaeodactylum tricornutum gene repertoire were described using 1,000 expressed sequence tags (ESTs). Subsequently, the number of ESTs was extended to 12,000 and the diatom EST database was constructed for functional analyses. These sequences have been used to make a comparative analysis between P. tricornutum and the putative complete proteomes from the green alga Chlamydomonas reinhardtii, the red alga Cyanidioschyzon merolae, and the diatom Thalassiosira pseudonana. The diatom EST database now consists of over 200,000 ESTs from P. tricornutum (16 libraries) and T. pseudonana (7 libraries) cells grown in a range of different conditions, many of which correspond to different abiotic stresses. Genome sequencing In 2004, the entire genome of the centric diatom, Thalassiosira pseudonana (32.4 Mb) was sequenced, followed in 2008 with the sequencing of the pennate diatom, Phaeodactylum tricornutum (27.4 Mb). Comparisons of the two reveal that the P. tricornutum genome includes fewer genes (10,402 opposed to 11,776) than T. pseudonana; no major synteny (gene order) could be detected between the two genomes. T. pseudonana genes show an average of ~1.52 introns per gene as opposed to 0.79 in P. tricornutum, suggesting recent widespread intron gain in the centric diatom. Despite relatively recent evolutionary divergence (90 million years), the extent of molecular divergence between centrics and pennates indicates rapid evolutionary rates within the Bacillariophyceae compared to other eukaryotic groups. Despite these genomic advancements, the integration of molecular methods in diatom research remains relatively low compared to other eukaryotic groups. Endosymbiotic gene transfer Diatom genomics brought much information about the extent and dynamics of the endosymbiotic gene transfer (EGT) process. Comparison of the T. pseudonana proteins with homologs in other organisms suggested that hundreds have their closest homologs in the Plantae lineage. EGT towards diatom genomes can be illustrated by the fact that the T. pseudonana genome encodes six proteins which are most closely related to genes encoded by the Guillardia theta (cryptomonad) nucleomorph genome. Four of these genes are also found in red algal plastid genomes, thus demonstrating successive EGT from red algal plastid to red algal nucleus (nucleomorph) to heterokont host nucleus. However, phylogenomic analyses of diatom proteomes and chromalveolate evolutionary history will likely take advantage of complementary genomic data from under-sequenced lineages such as red algae. Horizontal gene transfer In addition to EGT, horizontal gene transfer (HGT) can occur independently of an endosymbiotic event. The publication of the P. tricornutum genome reported that at least 587 P. tricornutum genes appear to be most closely related to bacterial genes, accounting for more than 5% of the P. tricornutum proteome. About half of these are also found in the T. pseudonana genome, attesting their ancient incorporation in the diatom lineage. Few molecular biology tools are currently available to generate mutants or transgenic lines : plasmids containing transgenes are inserted into the cells using the biolistic method or transkingdom bacterial conjugation (with 10−6 and 10−4 yield respectively and various transgenes have been successfully introduced and expressed in diatoms with stable transmissions through generations, and a more accurate comprehension of the diatoms' cellular processes. ==Human uses==

Paleontology Decomposition and decay of diatoms leads to organic and inorganic (in the form of silicates) sediment, the inorganic component of which can lead to a method of analyzing past marine environments by corings of ocean floors or bay muds, since the inorganic matter is embedded in deposition of clays and silts and forms a permanent geological record of such marine strata (see siliceous ooze). Industrial Diatoms, and their shells (frustules) as diatomite or diatomaceous earth, are important industrial resources used for fine polishing and liquid filtration. The complex structure of their microscopic shells has been proposed as a material for nanotechnology. Diatomite is considered to be a natural nano material and has many uses and applications such as: production of various ceramic products, construction ceramics, refractory ceramics, special oxide ceramics, for production of humidity control materials, used as filtration material, material in the cement production industry, initial material for production of prolonged-release drug carriers, absorption material in an industrial scale, production of porous ceramics, glass industry, used as catalyst support, as a filler in plastics and paints, purification of industrial waters, pesticide holder, as well as for improving the physical and chemical characteristics of certain soils, and other uses. Diatoms are also used to help determine the origin of materials containing them, including seawater. Nanotechnology The deposition of silica by diatoms may also prove to be of utility to nanotechnology. Diatom cells repeatedly and reliably manufacture valves of various shapes and sizes, potentially allowing diatoms to manufacture micro- or nano-scale structures which may be of use in a range of devices, including: optical systems; semiconductor nanolithography; and even vehicles for drug delivery. With an appropriate artificial selection procedure, diatoms that produce valves of particular shapes and sizes might be evolved for cultivation in chemostat cultures to mass-produce nanoscale components. It has also been proposed that diatoms could be used as a component of solar cells by substituting photosensitive titanium dioxide for the silicon dioxide that diatoms normally use to create their cell walls. Diatom biofuel producing solar panels have also been proposed. File:Supporting and regulating services provided by marine diatoms.png|alt=CNN = cloud condensation nuclei, DMS = dimethylsulphide, DMSP = dimethylsulfoniopropionate, VOCs = volatile organic compounds, dashed arrow: negative effect, solid arrow: positive effects| CNN = cloud condensation nuclei, DMS = dimethylsulphide, DMSP = dimethylsulfoniopropionate, VOCs = volatile organic compoundsdashed arrow: negative effect, solid arrow: positive effects Forensic The main goal of diatom analysis in forensics is to differentiate a death by submersion from a post-mortem immersion of a body in water. Laboratory tests may reveal the presence of diatoms in the body. Since the silica-based skeletons of diatoms do not readily decay, they can sometimes be detected even in heavily decomposed bodies. As they do not occur naturally in the body, if laboratory tests show diatoms in the corpse that are of the same species found in the water where the body was recovered, then it may be good evidence of drowning as the cause of death. The blend of diatom species found in a corpse may be the same or different from the surrounding water, indicating whether the victim drowned in the same site in which the body was found. ==History of discovery==

'' is a genus of freshwater diatoms, cuboid in shape with frustules (siliceous cell walls) attached at the corners so the colonies assume a zigzag shape. The first illustrations of diatoms are found in an article from 1703 in Transactions of the Royal Society showing unmistakable drawings of Tabellaria. Although the publication was authored by an unnamed English gentleman, there is recent evidence that he was Charles King of Staffordshire. The first formally identified diatom, the colonial Bacillaria paxillifera, was discovered and described in 1783 by Danish naturalist Otto Friedrich Müller. ==Gallery==

File:Surirella spiralis - SEM MUSE - sharpened.jpeg|Diatom Surirella spiralis File:Diatoms-HCMR.jpg|Diatoms Thalassiosira sp. on a membrane filter, pore size 0.4 μm. File:Paralia sulcata diatom.tif|Diatom Paralia sulcata. File:Achanthes trinodis - SEM MUSE.tiff|Diatom Achanthes trinodis File:Bacillaria paxillifera.jpg| Stand-alone cell of Bacillaria paxillifer File:Bacillaria paxillifer.tif| Colonial group of Bacillaria paxillifer Three diatom species were sent to the International Space Station, including the huge (6 mm length) diatoms of Antarctica and the exclusive colonial diatom, Bacillaria paradoxa. The cells of Bacillaria moved next to each other in partial but opposite synchrony by a microfluidics method. ==See also==