Diatom

Diatoms (diá-tom-os 'cut in half', from diá, 'through' or 'apart'; and the root of tém-n-ō, 'I cut'.)[10] are a major group of algae,[11] specifically microalgae, found in the oceans, waterways and soils of the world. Living diatoms make up a significant portion of the Earth's biomass: they generate about 20 to 50 percent of the oxygen produced on the planet each year,[12][13] take in over 6.7 billion metric tons of silicon each year from the waters in which they live,[14] and constitute nearly half of the organic material found in the oceans. The shells of dead diatoms can reach as much as a half-mile (800 m) deep on the ocean floor, and the entire Amazon basin is fertilized annually by 27 million tons of diatom shell dust transported by transatlantic winds from the African Sahara, much of it from the Bodélé Depression, which was once made up of a system of fresh-water lakes.[15][16]

For a molecule of two atoms, see Diatomic molecule.

Diatoms
Light microscopy of a sampling of marine diatoms found living between crystals of annual sea ice in Antarctica, showing a multiplicity of sizes, shapes, and colors
Scientific classification
Domain:
Eukaryota
(unranked):
SAR: a clade or supergroup that includes stramenopiles (heterokonts), alveolates, and Rhizaria.[1][2][3][4]
Superphylum:
Heterokonta
Phylum:
Ochrophyta
Class:
Bacillariophyceae

Synonyms

Diatoms are unicellular: they occur either as solitary cells or in colonies, which can take the shape of ribbons, fans, zigzags, or stars. Individual cells range in size from 2 to 200 micrometers.[17] In the presence of adequate nutrients and sunlight, an assemblage of living diatoms doubles approximately every 24 hours by asexual multiple fission; the maximum life span of individual cells is about six days.[18] Diatoms have two distinct shapes: a few (centric diatoms) are radially symmetric, while most (pennate diatoms) are broadly bilaterally symmetric. A unique feature of diatom anatomy is that they are surrounded by a cell wall made of silica (hydrated silicon dioxide), called a frustule.[19] These frustules have structural coloration due to their photonic nanostructure, prompting them to be described as "jewels of the sea" and "living opals". Movement in diatoms primarily occurs passively as a result of both water currents and wind-induced water turbulence; however, male gametes of centric diatoms have flagella, permitting active movement for seeking female gametes. Similar to plants, diatoms convert light energy to chemical energy by photosynthesis, although this shared autotrophy evolved independently in both lineages. Unusually for autotrophic organisms, diatoms possess a urea cycle, a feature that they share with animals, although this cycle is used to different metabolic ends in diatoms. The family Rhopalodiaceae also possess a cyanobacterial endosymbiont called a spheroid body. This endosymbiont has lost its photosynthetic properties, but has kept its ability to perform nitrogen fixation, allowing the diatom to fix atmospheric nitrogen.[20]

The study of diatoms is a branch of phycology. Diatoms are classified as eukaryotes, organisms with a membrane-bound cell nucleus, that separates them from the prokaryotes archaea and bacteria. Diatoms are a type of plankton called phytoplankton, the most common of the plankton types. Diatoms also grow attached to benthic substrates, floating debris, and on macrophytes. They comprise an integral component of the periphyton community.[21] Another classification divides plankton into eight types based on size: in this scheme, diatoms are classed as microalgae. Several systems for classifying the individual diatom species exist. Fossil evidence suggests that diatoms originated during or before the early Jurassic period, which was about 150 to 200 million years ago.

Diatoms are used to monitor past and present environmental conditions, and are commonly used in studies of water quality. Diatomaceous earth (diatomite) is a collection of diatom shells found in the earth's crust. They are soft, silica-containing sedimentary rocks which are easily crumbled into a fine powder and typically have a particle size of 10 to 200 μm. Diatomaceous earth is used for a variety of purposes including for water filtration, as a mild abrasive, in cat litter, and as a dynamite stabilizer.

Structure
Diagrammatic representation of a diatom.
1) Nucleus; holds the genetic material
2) Nucleolus; Location of the chromosomes
3) Golgi complex; modifies proteins and sends them out of the cell
4) Cell Wall; Outer membrane of the cell
5) Pyrenoid; center of carbon fixation
6) Chromatophore; pigment carrying membrane structure
7) Vacuoles; vesicle of a cell that contains fluid bound by a membrane
8) Cytoplasmic strands; hold the nucleus
9) Mitochondria; create ATP (energy) for the cell
10) Valves/Striae; allow nutrients in, and waste out, of the cell
Light microscopy of a living diatom.  Numbered graduations are 10 micrometres apart

Diatoms are 2 to 200 micrometers in length.[17] Their yellowish-brown chloroplasts, the site of photosynthesis, are typical of heterokonts, having four 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, except they lack the hairs (mastigonemes) characteristic in other groups.

Diatoms are often referred as "jewels of the sea" or "living opals" due to their optical properties.[22] 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.[23]

Diatoms build intricate hard but porous cell walls called frustules composed primarily of silica.[24]:25–30 This siliceous wall[25] 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).

Behaviour of diatoms
Planktonic diatoms such as Chaetoceros often grow in chains, and have features such as spines which slow sinking rates by increasing drag.

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.[26] 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.[27]

Some pennate diatoms are capable of a type of locomotion called "gliding", which allows them to move across surfaces via adhesive mucilage secreted through the raphe (an elongated slit in the valve face).[28][29] 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.

Biochemistry

Energy source

Diatoms are mainly photosynthetic; however a few are obligate heterotrophs and can live in the absence of light provided an appropriate organic carbon source is available.[30][31]

Silica metabolism

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.[32] 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-halves and grows a smaller half 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. This expands in size to give rise to a much larger cell, which then returns to size-diminishing divisions. Auxospore production is almost always linked to meiosis and sexual reproduction.

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.[33] 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.[34] In a phylogenetic study on silica transport genes from 8 diverse groups of diatoms, silica transport was found to generally group with species.[33] This study also found structural differences between the silica transporters of pennate (bilateral symmetry) and centric (radial symmetry) diatoms. The sequences compared in this study were used to create a diverse background in order to identify residues that differentiate function in the silica deposition process. Additionally, the same study found that a number of the regions were conserved within species, likely the base structure of silica transport.

These silica transport proteins are unique to diatoms, with no homologs found in other species, such as sponges or rice. The divergence of these silica transport genes is also indicative of the structure of the protein evolving from two repeated units composed of five membrane bound segments, which indicates either gene duplication or dimerization.[33] The silica deposition that takes place from the membrane bound vesicle in diatoms has been hypothesized to be a result of the activity of silaffins and long chain polyamines. This Silica Deposition Vesicle (SDV) has been characterized as an acidic compartment fused with Golgi-derived vesicles.[35] 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.

Urea cycle

A feature of diatoms is the urea cycle, which links them evolutionarily to animals. This was discovered in research carried out by Andrew Allen, Chris Bowler and colleagues. Their findings, published in 2011, that diatoms have a functioning urea cycle was highly significant, since prior to this, the urea cycle was thought to have originated with the metazoans which appeared several hundreds of millions of years after the diatoms. Their study showed that while diatoms and animals use the urea cycle for different ends, they are seen to be evolutionarily linked in such a way that animals and plants are not.[36]

Pigments

Major pigments of diatoms are chlorophylls a and c, beta-carotene, fucoxanthin, diatoxanthin and diadinoxanthin.[17]

Storage products

Storage products are chrysolaminarin and lipids.[24]

Life cycle
Sexual reproduction of a centric diatom (oogamy)
Sexual reproduction of a pinnate diatom (morphological isogamy, physiological anisogamy)

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.[17] It has been observed, however, that certain taxa have the ability to divide without causing a reduction in cell size.[37] 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.[17]

Cell division

Vegetative cells of diatoms are diploid (2N) and so meiosis can take place, producing male and female gametes which then fuse to form the zygote. The zygote sheds its silica theca and grows into a large sphere covered by an organic membrane, the auxospore. A new diatom cell of maximum size, the initial cell, forms within the auxospore thus beginning a new generation. Resting spores may also be formed as a response to unfavourable environmental conditions with germination occurring when conditions improve.[24]

Sperm motility

Diatoms are mostly non-motile; however, sperm found in some species can be flagellated, though motility is usually limited to a gliding motion.[24] In centric diatoms, the small male gametes have one flagellum while the female gametes are large and non-motile (oogamous). Conversely, in pennate diatoms both gametes lack flagella (isoogamous).[17] Certain araphid species, that is pennate diatoms without a raphe (seam), have been documented as anisogamous and are, therefore, considered to represent a transitional stage between centric and raphid pennate diatoms, diatoms with a raphe.[37]

Degradation by microbes

Certain species of bacteria in oceans and lakes can accelerate the rate of dissolution of silica in dead and living diatoms by using hydrolytic enzymes to break down the organic algal material.[38][39]

Classification

Structural
Shape classification of diatom frustules. The images are 3D models. The actual sizes of the frustules are about 10–80μm.[40]
Selections from Ernst Haeckel's 1904 Kunstformen der Natur (Art Forms of Nature), showing pennate (left) and centric (right) frustules.
Structure of a centric diatom frustule [40]

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.

Taxonomic

Relationship to other organisms
Light microscopy of several species of living freshwater diatoms

Diatoms belong to a large group called the heterokonts, which include both autotrophs such as golden algae and kelp; and heterotrophs such as water moulds. The classification of heterokonts is still unsettled: they may be designated 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[41] (other sources give a wider range of estimates[17][42][43][44]). Around 1,000-1,300 diatom genera have been described, both extant and fossil,[45][46] of which some 250-300 exist only as fossils.[47]

Classes and orders
Overview

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.

Today (writing at mid 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, and 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, and 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, is for some of the centric diatom orders considered 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 uses 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, while another analysis, that of 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.[48][49][50][51]

Round et al., 1990 treatment

Based on the fact that pennate diatoms either do or do not have a longitudinal groove in the valve, called a raphe,[52] a 1990 classification by Round, Crawford & Mann[42] divides the diatoms (as Bacillarophyta) into three classes, centric (22 orders); pennate without a raphe (12 orders); and pennate with a raphe (11 orders), as follows:[53]

Coscinodiscophyceae
Isthmia nervosaIsthmia nervosa
Coscinodiscophyceae
Odontella aurita
Thalassiosirales
Stephanodiscus hantzschii
Fragilaria through the microscope
  • Phylum Bacillarophyta (diatoms)
  • Subclass Biddulphiophycidae Round & R.M.Crawford
  • Subclass Chaetocerotophycidae Round & R.M.Crawford
  • Chaetocerotales Round & R.M.Crawford
  • Leptocylindrales Round & R.M.Crawford
  • Subclass Corethrophycidae Round & R.M.Crawford
  • Corethrales Round & R.M.Crawford
  • Subclass Coscinodiscophycidae Round & R.M.Crawford
  • Arachnoidiscales Round
  • Asterolamprales Round
  • Aulacoseirales R.M.Crawford
  • Chrysanthemodiscales Round
  • Coscinodiscales Round
  • Ethmodiscales Round
  • Melosirales R.M.Crawford
  • Orthoseirales R.M.Crawford
  • Paraliales R.M.Crawford
  • Stictocyclales Round
  • Stictodiscales Round & R.M.Crawford
  • Subclass Cymatosirophycidae Round & R.M.Crawford
  • Subclass Lithodesmiophycidae Round & R.M.Crawford
  • Lithodesmiales Round & R.M.Crawford
  • Subclass Rhizosoleniophycidae Round & R.M.Crawford
  • Rhizosoleniales Silva
  • Subclass Thalassiosirophycidae Round & R.M.Crawford
  • Subclass Fragilariophycidae Round
  • Ardissoneales Round
  • Climacospheniales Round
  • Cyclophorales Round & R.M.Crawford
  • Fragilariales P.C.Silva
  • Licmophorales Round
  • Protoraphidales Round
  • Rhabdonematales Round & R.M.Crawford
  • Rhaphoneidales Round
  • Striatellales Round
  • Tabellariales Round
  • Thalassionematales Round
  • Toxariales Round
  • Class Bacillariophyceae Haeckel, 1878, emend. D.G.Mann (pennate diatoms with a raphe (raphids))
  • Subclass Bacillariophycidae D.G.Mann
  • Subclass Eunotiophycidae D.G.Mann
Medlin & Kaczmarska, 2004 treatment

An alternate classification for the diatoms based on molecular phylogeny was proposed by Medlin & Kaczmarska in 2004, as follows.[54] Medlin and co-workers erected a new class, Mediophyceae (which could be re-ranked a subclass if diatoms as a whole are ranked as a class rather than a phylum) for the "polar centric" diatoms, which they consider to be more closely related to the pennate rather than to other centric diatoms, a concept which has been followed and/or further adapted by some (e.g. Adl et al., 2019, see below), but not all subsequent workers at this time.

  • Phylum Bacillariophyta (diatoms)
  • Subphylum Coscinodiscophytina
  • Arachnoidiscales
  • Asterolamprales
  • Aulacoseirales
  • Corethrales
  • Coscinodiscales
  • Chrysanthemodiscales
  • Ethmodiscales
  • Leptocylindrales
  • Melosirales
  • Orthoseirales
  • Rhizosoleniales
  • Stictocyclales
  • Stictodiscales
  • Subphylum Bacillariophytina
  • Class Mediophyceae ("polar centrics")
Ruggiero et al., 2015 treatment

In the treatment for "all life" (down to order, extant taxa only) by Ruggiero et al., 2015,[55] the diatoms are treated as follows. This treatment largely reflects that used by Algaebase as at 2015, and is also reflected in the current (mid 2020) treatment used in DiatomBase, the World Register of Marine Species (WoRMS) of which DiatomBase is a part, and the Catalogue of Life. This treatment is identical to that of Round et al., 1990, except that all diatoms are treated as a single class, Round et al.'s classes are reduced to subclasses, and the latter's original subclasses are omitted.

  • Superphylum Heterokonta (heterokonts: Ochrophyta plus other phyla))
  • Class Bacillariophyceae (diatoms)
  • Subclass Bacillariophycidae
  • Subclass Coscinodiscophycidae
  • Anaulales
  • Arachnoidiscales
  • Asterolamprales
  • Aulacoseirales
  • Biddulphiales
  • Chaetocerotales
  • Chrysanthemodiscales
  • Corethrales
  • Coscinodiscales
  • Cymatosirales
  • Ethmodiscales
  • Hemiaulales
  • Leptocylindrales
  • Lithodesmiales
  • Melosirales
  • Orthoseirales
  • Paraliales
  • Rhizosoleniales
  • Stictocyclales
  • Stictodiscales
  • Thalassiosirales
  • Triceratiales
  • Subclass Fragilariophycidae
  • Ardissoneales
  • Fragilariophycidae
  • Climacospheniales
  • Cyclophorales
  • Fragilariales
  • Licmophorales
  • Protoraphidales
  • Rhabdonematales
  • Rhaphoneidales
  • Striatellales
  • Tabellariales
  • Thalassionematales
  • Toxariales
Adl et al., 2019 treatment

Following earlier versions in the treatments of Adl et al. 2005 and 2012,[56][57] D.G. Mann, in Adl et al. 2019,[58] presented his most recent classification of diatoms as follows, 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 treats diatoms as a phylum (Diatomeae/Bacillariophyta), accepts the class Mediophyceae of Medlin and co-workers, introduces new subphyla and classes for a number of otherwise isolated genera, and re-ranks a number of previously established taxa as subclasses, but does not list orders or families. Inferred ranks have been added for clarity (Adl. et al. do not use ranks, but the intended ones in this portion of the classification are apparent from the choice of endings used, within the system of botanical nomenclature employed).

  • Clade Diatomista Derelle et al. 2016, emend. Cavalier-Smith 2017 (diatoms plus a subset of other ochrophyte groups)
  • Subphylum Leptocylindrophytina D.G. Mann in Adl et al. 2019
  • Class Leptocylindrophyceae D.G. Mann in Adl et al. 2019 (Leptocylindrus, Tenuicylindrus)
  • Class Corethrophyceae D.G. Mann in Adl et al. 2019 (Corethron)
  • Subphylum Ellerbeckiophytina D.G. Mann in Adl et al. 2019 (Ellerbeckia)
  • Subphylum Probosciophytina D.G. Mann in Adl et al. 2019 (Proboscia)
  • Subphylum Melosirophytina D.G. Mann in Adl et al. 2019 (Aulacoseira, Melosira, Hyalodiscus, Stephanopyxis, Paralia, Endictya)
  • Subphylum Coscinodiscophytina Medlin & Kaczmarska 2004, emend. (Actinoptychus, Coscinodiscus, Actinocyclus, Asteromphalus, Aulacodiscus, Stellarima)
  • Subphylum Rhizosoleniophytina D.G. Mann in Adl et al. 2019 (Guinardia, Rhizosolenia, Pseudosolenia)
  • Subphylum Arachnoidiscophytina D.G. Mann in Adl et al. 2019 (Arachnoidiscus)
  • Subphylum Bacillariophytina Medlin & Kaczmarska 2004, emend.
  • Class Mediophyceae Jouse & Proshkina-Lavrenko in Medlin & Kaczmarska 2004
  • Subclass Chaetocerotophycidae Round & R.M. Crawford in Round et al. 1990, emend.
  • Subclass Lithodesmiophycidae Round & R.M. Crawford in Round et al. 1990, emend.
  • Subclass Thalassiosirophycidae Round & R.M. Crawford in Round et al. 1990
  • Subclass Cymatosirophycidae Round & R.M. Crawford in Round et al. 1990
  • Subclass Odontellophycidae D.G. Mann in Adl et al. 2019
  • Subclass Chrysanthemodiscophycidae D.G. Mann in Adl et al. 2019
  • Class Biddulphiophyceae D.G. Mann in Adl et al. 2019
  • Subclass Biddulphiophycidae Round and R.M. Crawford in Round et al. 1990, emend.
  • Biddulphiophyceae incertae sedis (Attheya)
  • Bacillariophyceae incertae sedis (Striatellaceae)
  • Subclass Urneidophycidae Medlin 2016
  • Subclass Fragilariophycidae Round in Round, Crawford & Mann 1990, emend.
  • Subclass Bacillariophycidae D.G. Mann in Round, Crawford & Mann 1990, emend.
Others

Another systematic approach to classification was proposed in 1995, the Hoek, Mann and Jahns system.[59] Previous versions of the Adl et al., 2019 classification appeared in Adl et al. 2005 and Adl et al. 2012,[56][57] also in the chapter "Bacillariophyta" by Mann, Crawford & Round in the 2017 Handbook of the Protists edited by Archibald et al.,[60] in which some groups later named as formal taxa are listed under informal names (leptocylindrids, corethrids, melosirids, etc.).

  • Scanning electron microscope images
  • Diatom Surirella spiralis
  • Diatoms Chaetoceros spp. on a membrane filter, pore size 0.4 μm.
  • Diatom Paralia sulcata.
  • Diatom Achanthes trinodis

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),[61] although the molecular clock[61] and sedimentary[62] 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.[63] 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.[64] 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 silicon cycle
Further information: Silica cycle

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.[65][66][67] 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.[68] 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,[69] 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).[70]

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.[71][72] 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.[73]

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,[74] 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.[73]

Method of investigation

The fossil record of diatoms has largely been established through the recovery of their siliceous frustules in marine and non-marine sediments. Although diatoms have both a marine and non-marine stratigraphic record, diatom biostratigraphy, which is based on time-constrained evolutionary originations and extinctions of unique taxa, is only well developed and widely applicable in marine systems. The duration of diatom species ranges have been documented through the study of ocean cores and rock sequences exposed on land.[75] 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 <100,000 years, although typical age resolution for Cenozoic diatom assemblages is several hundred thousand years.

Diatoms preserved in lake sediments are widely used for paleoenvironmental reconstructions of Quaternary climate, especially for closed-basin lakes which experience fluctuations in water depth and salinity.

Diversification

The Cretaceous record of diatoms is limited, but recent studies reveal a progressive diversification of diatom types. The Cretaceous–Paleogene extinction event, which in the oceans dramatically affected organisms with calcareous skeletons, appears to have had relatively little impact on diatom evolution.[76]

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,[77] and at the Eocene–Oligocene boundary.[78] Further turnover of assemblages took place at various times between the middle Miocene and late Pliocene,[79] 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.[75] 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).[80] Subsequently, the number of ESTs was extended to 12,000 and the diatom EST database was constructed for functional analyses.[81] 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.[82] 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.[83]

Genome sequencing

In 2004, the entire genome of the centric diatom, Thalassiosira pseudonana (32.4 Mb) was sequenced,[84] followed in 2008 with the sequencing of the pennate diatom, Phaeodactylum tricornutum (27.4 Mb).[85] 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.[85][86] 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.[85] Comparative genomics also established that a specific class of transposable elements, the Diatom Copia-like retrotransposons (or CoDis), has been significantly amplified in the P. tricornutum genome with respect to T. pseudonana, constituting 5.8 and 1% of the respective genomes.[87]

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.[84] More recent phylogenomic analyses of diatom proteomes provided evidence for a prasinophyte-like endosymbiont in the common ancestor of chromalveolates as supported by the fact the 70% of diatom genes of Plantae origin are of green lineage provenance and that such genes are also found in the genome of other stramenopiles. Therefore, it was proposed that chromalveolates are the product of serial secondary endosymbiosis first with a green algae, followed by a second one with a red algae that conserved the genomic footprints of the previous but displaced the green plastid.[88] 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.[85]

Ecology

Distribution
Regions of high abundance of Diatoms in the ocean

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.[89] Most live pelagically in open water, although some live as surface films at the water-sediment interface (benthic), or even under damp atmospheric conditions. They are especially important in oceans, where they contribute an estimated 45% of the total oceanic primary production of organic material.[90] Spatial distribution of marine phytoplankton species is restricted both horizontally and vertically.[91][24]

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[89] 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).

Contribution to modern oceanic silicon cycle
A diagram of the modern oceanic silicon cycle showing the major flows and their magnitudes. The majority of "Biological Production" of biogenic silica in the ocean is driven by diatoms. These extract dissolved silicic acid in surface waters during growth, with this returned by recycling throughout the water column after they die. Inputs of silicon to the ocean from "above" arrive via rivers and aeolian dust, while those from "below" include seafloor sediment recycling, weathering, and hydrothermal activity. Fluxes are shown in T mol Si y−1 (where 1 Tmol Si y−1 = 28 million metric tons of silicon per year).[92]

Diatoms contribute in a significant way to the modern oceanic silicon cycle: they are the source of the vast majority of biological production.

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.[93][94] The problem is most frequently recorded from Australia and New Zealand.[95]

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[96]), 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[96][97] (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.[90][92]

Reason for success
Egge & Aksnes (1992) figure.[98]

Diatoms are ecologically successful, and occur in virtually every environment that contains water – not only oceans, seas, lakes, and streams, but also soil and wetlands. The use of silicon by diatoms is believed by many researchers to be the key to this ecological success. Raven (1983)[99] 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)[98] found that diatom dominance of mesocosm communities was directly related to the availability of silicic acid – when concentrations were greater than 2 µmol m−3, they found that diatoms typically represented more than 70% of the phytoplankton community. Other researchers[100] 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, notwithstanding these possible advantages conferred by their use of silicon, diatoms typically have higher growth rates than other algae of the same corresponding size.[89]

Sources for collection

Diatoms may be obtained from multiple sources.[101]

Marine

Marine diatoms can be collected by direct water sampling, and benthic forms can be secured by scraping barnacles, oyster and other shells.

Fresh waters

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.

Algae and plants

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.

Animal alimentary tracts

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.

Cultivation

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.

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
Diatomaceous earth as viewed under bright field illumination on a light microscope. This image consists of a mixture of centric (radially symmetric) and pennate (bilaterally symmetric) diatoms suspended in water. The scale is 6.236 pixels/μm, the image is 1.13 by 0.69 mm.

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.[102]

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. [103] [104] [105]

Diatoms are also used to help determine the origin of materials containing them, including seawater.

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.[106]

Nanotechnology

The deposition of silica by diatoms may also prove to be of utility to nanotechnology.[107] 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.[108] 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.[109] Diatom biofuel producing solar panels have also been proposed.[110]

History of discovery

The first diatom formally described in scientific literature, the colonial Bacillaria paradoxa, was discovered in 1783 by Danish naturalist Otto Friedrich Müller.

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