diatom n : microscopic unicellular marine or freshwater colonial alga having cell walls impregnated with silica
EtymologyFrom (dia) 'through' + (temnein) 'to cut', i.e., "cut in half"
- Finnish: piilevä
Diatoms (Greek: (dia) = "through" + (temnein) = "to cut", i.e., "cut in half") are a major group of eukaryotic algae, and are one of the most common types of phytoplankton. Most diatoms are unicellular, although they can exist as colonies in the shape of filaments or ribbons (e.g. Fragillaria), fans (Meridion), zigzags (Tabellaria), or stellate colonies (Asterionella). A characteristic feature of diatom cells is that they are encased within a unique cell wall made of silica (hydrated silicon dioxide) called a frustule. These frustules show a wide diversity in form, some quite beautiful and ornate, but usually consist of two asymmetrical sides with a split between them, hence the group name. Fossil evidence suggests that they originated during, or before, the early Jurassic Period. Diatom communities are a popular tool for monitoring environmental conditions, past and present, and are commonly used in studies of water quality.
General biologyThere are more than 200 genera of living diatoms, and it is estimated that there are approximately 100,000 extant species. Diatoms are a widespread group and can be found in the oceans, in freshwater, in soils and on damp surfaces. 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 are estimated to contribute up to 45% of the total oceanic primary production. Although usually microscopic, some species of diatoms can reach up to 2 millimetres in length.
Diatoms belong to a large group called the heterokonts, including both autotrophs (e.g. golden algae, kelp) and heterotrophs (e.g. water moulds). Their yellowish-brown chloroplasts are typical of heterokonts, with four membranes and containing pigments such as fucoxanthin. Individuals usually lack flagella, but they are present in gametes and have the usual heterokont structure, except they lack the hairs (mastigonemes) characteristic in other groups. Most diatoms are non-motile, although some move via flagellation. As their relatively dense cell walls cause them to readily sink, planktonic forms in open water usually rely on turbulent mixing of the upper layers by the wind to keep them suspended in sunlit surface waters. Some species actively regulate their buoyancy with intracellular lipids to counter sinking
Diatoms cells are contained within a unique silicate (silicic acid) cell wall comprising two separate valves (or shells). The biogenic silica that the cell wall is composed of is synthesised intracellularly by the polymerisation of silicic acid monomers. This material is then extruded to the cell exterior and added to the wall. Diatom cell walls are also called frustules or tests, and their two valves typically overlap one other like the two halves of a petri dish. 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 vegetatively, 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.
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.
The classification of heterokonts is still unsettled, and they may be treated as a division (or phylum), kingdom, or something in-between. Accordingly, groups like the diatoms may be ranked anywhere from class (usually called Bacillariophyceae) to division (usually called Bacillariophyta), with corresponding changes in the ranks of their subgroups. The diatoms are also sometimes referred to as Class Diatomophyceae.
Diatoms are traditionally divided into two orders: centric diatoms (Centrales), which are radially symmetric, and pennate diatoms (Pennales), which are bilaterally symmetric. The former are paraphyletic to the latter. A more recent classification provide more comprehensive coverage of diatom taxonomy.
Planktonic forms 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 (e.g. at the start of spring) their competitive edge allows them to quickly 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).
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 inimical 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 condition that typically causes diatom (spring) blooms to end is a lack of silicon. Unlike other nutrients, this is only a major requirement of diatoms so 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 lifestyle, diatoms are believed to play a disproportionately important role in the export of carbon from oceanic surface waters.
The use of silicon by diatoms is believed by many researchers to be the key to their ecological success. In a now classic study, Egge & Aksnes (1992) 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. Other researchers 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). Notwithstanding the possible advantages conferred by silicon, diatoms typically have higher growth rates than other algae of a corresponding size, although recent 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 deposits of fossil diatoms found as far back as the early Cretaceous, and some rocks (diatomaceous earth, diatomite, kieselguhr) being composed almost entirely of them.
Although the diatoms may have existed since the Triassic, the timing of their ascendancy and "take-over" of the silicon cycle is more recent. 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" is unclear, and different authors have conflicting interpretations of the fossil record. Some evidence, such as the eviction of siliceous sponges from the shelves, suggests that this takeover began in the Cretaceous (146 Ma to 65 Ma), while evidence from radiolarians suggests "take-over" did not begin until the Cenozoic (65 Ma to present). Nevertheless, regardless of the details of the "take-over" timing, it is clear that this most recent revolution has installed much tighter biological control over the biogeochemical cycle of silicon.
CollectionLiving 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. 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. They 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.
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. Marine diatoms can be collected by direct water sampling, though benthic forms can be secured by scraping barnacles, oyster shells, and other shells.
The silicious shells of diatoms are among the most beautiful objects which can be examined with the microscope. To obtain perfectly clean mounts requires considerable time and patience, but once the material is cleaned, preparations may be made at any time with very little trouble.
This section uses text from Methods in Plant Histology.
Genome sequencingThe entire genome of the centric diatom, Thalassiosira pseudonana, has been sequenced, and the sequencing of a second diatom genome from the pennate diatom Phaeodactylum tricornutum is in progress. The first insights into the genome properties of the P. tricornutum gene repertoire was described using 1,000 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 centric diatom T. pseudonana.
Nanotechnology researchThe self-replicating properties of diatoms prove to be a great resource for nanotechnologists who desire to reproduce these properties. Using genome mapping, biologists and nanotechnologists can isolate the proteins which assist in the deposition of silica during division. With knowledge of the self-replicating properties, nanotechnologists can mimic this construction for various nanoscale 'widgets', optical systems, and materials for the semiconductor industry. It may also be possible to use diatom shells as vehicles for drug delivery. The development of a compustat can select certain diatom species by their properties and match them with nanotechnologies that would be most useful. These small organisms can help biologists and nanotechnologists to work together to further research.
- Computer simulations of pattern formation in diatoms
- Catalogue of Diatom Names, California Academy of Sciences
- Diatom Genome, Joint Genome Institute
- Diatom EST database, École Normale Supérieure
- Plankton*Net, taxonomic database including images of diatom species
- Life History and Ecology of Diatoms, University of California Museum of Paleontology
- Diatoms: 'Nature's Marbles', Eureka site, University of Bergen
- Diatom life history and ecology, Microfossil Image Recovery and Circulation for Learning and Education (MIRACLE), University College London
- [http://220.127.116.11/rbge/web/science/research/crypto/diatom.jsp Diatom page], Royal Botanic Garden Edinburgh
- Geometry and Pattern in Nature 3: The holes in radiolarian and diatom tests
- Art Deco Diatoms, Wim van Egmond
diatom in Czech: Rozsivky
diatom in Danish: Kiselalge
diatom in German: Kieselalgen
diatom in Estonian: Ränivetikad
diatom in Spanish: Diatomea
diatom in Esperanto: Diatomo
diatom in Basque: Diatomea
diatom in French: Bacillariophyta
diatom in Korean: 규조류
diatom in Croatian: Alge kremenjašice
diatom in Indonesian: Diatom
diatom in Icelandic: Kísilþörungar
diatom in Italian: Diatomee
diatom in Hebrew: צורניות
diatom in Georgian: კაჟოვანი წყალმცენარეები
diatom in Lithuanian: Titnagdumbliai
diatom in Hungarian: Kovamoszatok
diatom in Macedonian: Силикатни алги
diatom in Dutch: Diatomee
diatom in Japanese: 珪藻
diatom in Norwegian: Kiselalger
diatom in Norwegian Nynorsk: Diatomèr
diatom in Polish: Okrzemki
diatom in Portuguese: Diatomácea
diatom in Russian: Диатомовые водоросли
diatom in Simple English: Diatom
diatom in Slovak: Rozsievky
diatom in Serbian: Силикатне алге
diatom in Finnish: Piilevät
diatom in Swedish: Kiselalger
diatom in Turkish: Diatomlar
diatom in Chinese: 矽藻