Ditylum brightwellii

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Ditylum brightwellii
Ditylum brightwellii2.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Stramenopiles
Phylum: Gyrista
Subphylum: Ochrophytina
Class: Bacillariophyceae
Order: Lithodesmiales
Family: Lithodesmiaceae
Genus: Ditylum
Species:
D. brightwellii
Binomial name
Ditylum brightwellii
(T.West) Grunow in Van Heurck

Ditylum brightwellii is a species of cosmopolitan marine centric diatoms. It is a unicellular photosynthetic autotroph that has the ability to divide rapidly and contribute to spring phytoplankton blooms. [1]

Description

The D. brightwellii cell has a high length to diameter ratio. The cell wall is silicified, as is characteristic of all diatoms. This hard, porous covering is known as the frustule and causes the cell to be more dense than the surrounding water. Oceanic currents and surface winds prevent D. brightwellii cells from sinking beneath the euphotic zone. Cells range in size from 25–100μm in diameter and 80–130μm in length. [2] The valve is most often triangular in shape, but can also be biangular or quadrangular. [3] A long hollow tube called the rimoportula is located centrally and extends from each valve [3]

Distribution

Ditylum brightwellii is found in all global oceans except in polar waters. [2] Genetically distinct populations were observed over the course of a spring bloom in Puget Sound, suggesting that certain genetic lineages are better adapted to certain environmental conditions. [4]

Il est le plus fort des platons vertébrés du 21ème siècle.

Life cycle

Sample in Black Sea Dytilum Brightwelli 3.jpg
Sample in Black Sea

Ditylum brightwellii reproduces primarily asexually, creating clonal lineages. [5] Vegetative cells are capable of enlargement and may also produce resting spores. [5] However, samples from Puget Sound, WA display high genetic diversity. [4] This is indicative of sexual reproduction (auxospore formation). Clonal isolates have observed to produce both sperm and eggs. [6] Two eggs are produced from each oogonium and 64 sperm are produced from each spermatogonangium. [6] The frequency of sexual reproduction in D. brightwellii is not clear, although conditions including increased nutrients, temperatures ranging from 10 °C-14 °C, and a short photoperiod may be favorable for sexual reproduction. [6]

Related Research Articles

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A diatom is any member of a large group comprising several genera of algae, 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, take in over 6.7 billion tonnes of silicon each year from the waters in which they live, 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 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.

<span class="mw-page-title-main">Phytoplankton</span> Autotrophic members of the plankton ecosystem

Phytoplankton are the autotrophic (self-feeding) components of the plankton community and a key part of ocean and freshwater ecosystems. The name comes from the Greek words φυτόν, meaning 'plant', and, meaning 'wanderer' or 'drifter'.

<span class="mw-page-title-main">Spring bloom</span> Strong increase in phytoplankton abundance that typically occurs in the early spring

The spring bloom is a strong increase in phytoplankton abundance that typically occurs in the early spring and lasts until late spring or early summer. This seasonal event is characteristic of temperate North Atlantic, sub-polar, and coastal waters. Phytoplankton blooms occur when growth exceeds losses, however there is no universally accepted definition of the magnitude of change or the threshold of abundance that constitutes a bloom. The magnitude, spatial extent and duration of a bloom depends on a variety of abiotic and biotic factors. Abiotic factors include light availability, nutrients, temperature, and physical processes that influence light availability, and biotic factors include grazing, viral lysis, and phytoplankton physiology. The factors that lead to bloom initiation are still actively debated.

<span class="mw-page-title-main">Holoplankton</span>

Holoplankton are organisms that are planktic for their entire life cycle. Holoplankton can be contrasted with meroplankton, which are planktic organisms that spend part of their life cycle in the benthic zone. Examples of holoplankton include some diatoms, radiolarians, some dinoflagellates, foraminifera, amphipods, krill, copepods, and salps, as well as some gastropod mollusk species. Holoplankton dwell in the pelagic zone as opposed to the benthic zone. Holoplankton include both phytoplankton and zooplankton and vary in size. The most common plankton are protists.

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Phaeodactylum tricornutum is a diatom. It is the only species in the genus Phaeodactylum. Unlike other diatoms, P. tricornutum can exist in different morphotypes and changes in cell shape can be stimulated by environmental conditions. This feature can be used to explore the molecular basis of cell shape control and morphogenesis. Unlike most diatoms, P. tricornutum can grow in the absence of silicon and can survive without making silicified frustules. This provides opportunities for experimental exploration of silicon-based nanofabrication in diatoms.

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Phycotoxins are complex allelopathic chemicals produced by eukaryotic and prokaryotic algal secondary metabolic pathways. More simply, these are toxic chemicals synthesized by photosynthetic organisms. These metabolites are not harmful to the producer but may be toxic to either one or many members of the marine food web. This page focuses on phycotoxins produced by marine microalgae; however, freshwater algae and macroalgae are known phycotoxin producers and may exhibit analogous ecological dynamics. In the pelagic marine food web, phytoplankton are subjected to grazing by macro- and micro-zooplankton as well as competition for nutrients with other phytoplankton species. Marine bacteria try to obtain a share of organic carbon by maintaining symbiotic, parasitic, commensal, or predatory interactions with phytoplankton. Other bacteria will degrade dead phytoplankton or consume organic carbon released by viral lysis. The production of toxins is one strategy that phytoplankton use to deal with this broad range of predators, competitors, and parasites. Smetacek suggested that "planktonic evolution is ruled by protection and not competition. The many shapes of plankton reflect defense responses to specific attack systems". Indeed, phytoplankton retain an abundance of mechanical and chemical defense mechanisms including cell walls, spines, chain/colony formation, and toxic chemical production. These morphological and physiological features have been cited as evidence for strong predatory pressure in the marine environment. However, the importance of competition is also demonstrated by the production of phycotoxins that negatively impact other phytoplankton species. Flagellates are the principle producers of phycotoxins; however, there are known toxigenic diatoms, cyanobacteria, prymnesiophytes, and raphidophytes. Because many of these allelochemicals are large and energetically expensive to produce, they are synthesized in small quantities. However, phycotoxins are known to accumulate in other organisms and can reach high concentrations during algal blooms. Additionally, as biologically active metabolites, phycotoxins may produce ecological effects at low concentrations. These effects may be subtle, but have the potential to impact the biogeographic distributions of phytoplankton and bloom dynamics.

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References

  1. Rynearson, Tatiana A.; Armbrust, E. Virginia (2005). "Maintenance of clonal diversity during a spring bloom of the centric diatom Ditylum brightwellii". Molecular Ecology. 14 (6): 1631–1640. doi:10.1111/j.1365-294X.2005.02526.x. PMID   15836638. S2CID   39671471.
  2. 1 2 "Ditylum brightwellii". Smithsonian Institution. 25 September 2011. Retrieved 4 November 2013.
  3. 1 2 "Ditylum J.W.Bailey, 1861: 163". Algaebase. Retrieved 4 November 2013.
  4. 1 2 Rynearson, T. A.; Newton, J. A.; Armbrust, E. V. (2006). "Spring bloom development, genetic variation, and population succession in the planktonic diatom Ditylum brightwellii". Limnology and Oceanography. 51 (3): 1249–1261. Bibcode:2006LimOc..51.1249R. doi:10.4319/lo.2006.51.3.1249.
  5. 1 2 Hargraves PE (1984) Resting spore formation in the marine diatom Ditylum brightwellii (West) Grun. ex V.H. In: Proceedings of the Seventh International Diatom Symposium, Philadelphia, 22–27 August 1982 (ed. Mann DG), pp. 33–46. Otto Koeltz-Science, Koenigstein.
  6. 1 2 3 Koester, Julie A.; Brawley, Susan H.; Karp-Boss, Lee; Mann, David G. (2007). "Sexual reproduction in the marine centric diatom Ditylum brightwellii (Bacillariophyta)". European Journal of Phycology. 42 (4): 351–366. doi: 10.1080/09670260701562100 . ISSN   0967-0262. S2CID   80737380.

Further reading