Emiliania huxleyi

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Emiliania huxleyi
A scanning electron micrograph of a single Emiliania huxleyi cell.
Scientific classification
(incertae sedis within Eukaryota)
Domain:
Eukaryota
(unranked):
Haptophyta
Class:
Prymnesiophyceae
Order:
Isochrysidales
Family:
Noelaerhabdaceae
Genus:
Emiliania
Species:
E. huxleyi
Binomial name
Emiliania huxleyi
(Lohm.) Hay and Mohler

Emiliania huxleyi, often abbreviated "EHUX", is a species of coccolithophore with a global distribution from the tropics to subarctic waters. It is one of thousands of different photosynthetic plankton that freely drift in the euphotic zone of the ocean, forming the basis of virtually all marine food webs. It is studied for the extensive blooms it forms in nutrient-depleted waters after the reformation of the summer thermocline. Like other coccolithophores, E. huxleyi is a single-celled phytoplankton covered with uniquely ornamented calcite disks called coccoliths (also informally known as liths or scales). Individual coccoliths are abundant in marine sediments although complete coccospheres are more unusual. In the case of E. huxleyi, not only the shell, but also the soft part of the organism may be recorded in sediments. It produces a group of chemical compounds that are very resistant to decomposition. These chemical compounds, known as alkenones, can be found in marine sediments long after other soft parts of the organisms have decomposed. Alkenones are most commonly used by earth scientists as a means to estimate past sea surface temperatures.

Basic facts

Emiliania huxleyi was named after Thomas Huxley and Cesare Emiliani, who were the first to examine sea-bottom sediment and discover the coccoliths within it. It is the most numerically abundant and widespread coccolithophore species. Its coccoliths are transparent and commonly colourless, but are formed of calcite which refracts light very efficiently in the water column. This, and the high concentrations caused by continual shedding of their coccoliths makes E. huxleyi blooms easily visible from space. Satellite images show that blooms can cover large areas, with complementary shipboard measurements indicating that E. huxleyi is by far the dominant phytoplankton species under these conditions. This species has been an inspiration for James Lovelock's Gaia hypothesis which claims that living organisms collectively self-regulate biogeochemistry and climate at nonrandom metastable states.

Abundance and distribution

E. huxleyi is by far the most abundant coccolithophore found in the Earth's oceans, and is considered ubiquitous, occurring everywhere except the polar regions. During massive blooms (which can cover over 100,000 square kilometers), EHUX cell concentrations can outnumber those of all other species in the region combined, accounting for 75% or more of the total number of photosynthetic plankton in the area. EHUX blooms regionally act as an important source of calcium carbonate and dimethyl sulfide, the massive production of which can have a significant impact not only on the properties of the surface mixed layer, but also on global climate. The blooms can be identified through satellite imagery because of the large amount of light back-scattered from the water column, which provides a method to assess their biogeochemical importance on both basin and global scales. These blooms are prevalent in the Norwegian fjords, causing satellites to pick up "white waters", which describes the reflectance of the blooms picked up by satellites. This is due to the mass of coccoliths reflecting the incoming sunlight back out of the water, allowing the extent of EHUX blooms to be distinguished in fine detail.

Extensive E. huxleyi blooms can have a visible impact on sea albedo. While multiple scattering can increase light path per unit depth, increasing absorption and solar heating of the water column, EHUX has inspired proposals for geomimesis,[1] because micron-sized air bubbles are specular reflectors, and so in contrast to E. huxleyi, tend to lower the temperature of the upper water column. As with self-shading within water-whitening coccolithophore plankton blooms, this may reduce photosynthetic productivity by altering the geometry of the euphotic zone. Both experiments and modeling are needed to quantify the potential biological impact of such effects, and the corollary potential of reflective blooms of other organisms to increase or reduce evaporation and methane evolution by altering fresh water temperatures.

Biogeochemical impacts

Climate change

As with all phytoplankton, primary production of EHUX through photosynthesis is a sink of carbon dioxide. However, the production of coccoliths through calcification is a source of CO2. This means that coccolithophores, including EHUX, have the potential to act as a net source of CO2 out of the ocean. Whether they are a net source or sink and how they will react to ocean acidification is not well understood.

Ocean heat retention

Scattering stimulated by EHUX blooms not only causes more heat and light to be pushed back up into the atmosphere than usual, but also cause more of the remaining heat to be trapped closer to the ocean surface. This is problematic because it is the surface water that exchanges heat with the atmosphere, and EHUX blooms may tend to make the overall temperature of the water column dramatically cooler over longer time periods. However, the importance of this effect, whether positive or negative, is currently being researched and has not yet been established.

See also

Notes

  1. ^ Seitz, R. (2011). Bright water: Hydrosols, water conservation, and climate change. Climatic Change, 105:365-381.

References

  • Amouroux, D.; P. S. Liss; E. Tessier; M. Hamren-Larsson; O. F. X. Donard (2001). "Role of oceans as biogenic sources of selenium". Earth and Planetary Science Letters. 189 (3–4): 277–283. Bibcode:2001E&PSL.189..277A. doi:10.1016/S0012-821X(01)00370-3.
  • Andreae, M. O.; P. J. Crutzen (1997-05-16). "Atmospheric aerosols: biogeochemical sources and role in atmospheric chemistry". Science. 276 (5315): 1052–1058. doi:10.1126/science.276.5315.1052. Retrieved 2008-03-21.
  • Araie, H.; T. Obata; Y. Shiraiwa (2003). "Metabolism of selenium in a coccolithophorid, Emiliania huxleyi". J Plant Res. 116: 119.
  • Boisson, F.; C. S. Karez; M. Henry; M. Romeo; M. Gnassia-Barelli (1996). "Ultrastructural observations on the marine coccolithophorid Cricosphaera elongata cultured in the presence of selenium or cadmium". Bulletin de l'Institut océanographique(Monaco): 239–247.
  • Dacey, J. W. H.; S. Wakeham (1986-09-19). "Oceanic dimethylsulfide: Production during zooplankton grazing on phytoplankton". Science. 233 (4770): 1314–1316. Bibcode:1986Sci...233.1314D. doi:10.1126/science.233.4770.1314. PMID 17843360. Retrieved 2008-03-21.
  • Dambara, A.; Y. Shiraiwa (1999). "Requirement of selenium for the growth and selection of adequate culture media in a marine coccolithophorid, Emiliania huxleyi". Bulletin of the Society of Sea Water Science, Japan. 53 (6): 476–484.
  • Danbara, A.; Y. Shiraiwa (2007). "The requirement of selenium for the growth of marine coccolithophorids, Emiliania huxleyi, Gephyrocapsa oceanica and Helladosphaera sp. (Prymnesiophyceae)". Plant and Cell Physiology. 40 (7): 762–766. doi:10.1093/oxfordjournals.pcp.a029603.
  • DeBose, J. L.; S. C. Lema; G. A. Nevitt (2008-03-07). "Dimethylsulfoniopropionate as a foraging cue for reef fishes". Science. 319 (5868): 1356. Bibcode:2008Sci...319.1356D. doi:10.1126/science.1151109. PMID 18323445. Retrieved 2008-03-21.
  • Doblin, M. A.; S. I. Blackburn; G. M. Hallegraeff (1999). "Growth and biomass stimulation of the toxic dinoflagellate Gymnodinium catenatum (Graham) by dissolved organic substances". Journal of Experimental Marine Biology and Ecology. 236 (1): 33–47. doi:10.1016/S0022-0981(98)00193-2.
  • Fabry, V. J. (2003). Calcium carbonate production by coccolithophorid algae in long-term carbon dioxide sequestration. California State University, San Marcos (US).
  • Howard, E. C.; et al. (2006-10-27). "Bacterial taxa that limit sulfur flux from the ocean". Science. 314 (5799): 649–652. Bibcode:2006Sci...314..649H. doi:10.1126/science.1130657. PMID 17068264. Retrieved 2008-03-21.
  • Norici, A.; R. Hell; M. Giordano (2005). "Sulfur and primary production in aquatic environments: An ecological perspective". Photosynthesis Research. 86 (3): 409–417. doi:10.1007/s11120-005-3250-0. PMID 16307310.
  • Obata, T.; Y. Shiraiwa (2005). "A novel eukaryotic selenoprotein in the haptophyte alga Emiliania huxleyi". Journal of Biological Chemistry. 280 (18): 18462–8. doi:10.1074/jbc.M501517200. PMID 15743763.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  • Obata, T.; H. Araie; Y. Shiraiwa (2003). "Kinetic studies on bioconcentration mechanism of selenium by a coccolithophorid, Emiliania huxleyi". Plant Cell Physiology. 44: S43.
  • Obata, T.; H. Araie; Y. Shiraiwa (2004). "Bioconcentration mechanism of selenium by a coccolithophorid, Emiliania huxleyi". Plant Cell Physiology. 45 (10): 1434–1441. doi:10.1093/pcp/pch164. PMID 15564527. Retrieved 2008-03-21.
  • Read, B.; J. Kegel; MJ. Klute (2013). "Pan genome of the phytoplankton Emiliania underpins its global distribution". Nature. 499 (7457): 209–213. Bibcode:2013Natur.499..209.. doi:10.1038/nature12221. PMID 23760476.
  • Shiraiwa, Y. (2003). "Physiological regulation of carbon fixation in the photosynthesis and calcification of coccolithophorids". Comparative Biochemistry and Physiology B. 136 (4): 775–783. doi:10.1016/S1096-4959(03)00221-5.
  • Sorrosa, J. M.; M. Satoh; Y. Shiraiwa (2005). "Low temperature stimulates cell enlargement and intracellular calcification of coccolithophorids". Marine Biotechnology. 7 (2): 128–133. doi:10.1007/s10126-004-0478-1. PMID 15782289.
  • Todd, J. D.; et al. (2007-02-02). "Structural and regulatory genes required to make the gas dimethyl sulfide in bacteria". Science. 315 (5812): 666–669. Bibcode:2007Sci...315..666T. doi:10.1126/science.1135370. PMID 17272727. Retrieved 2008-03-21.
  • Vallina, S. M.; R. Simo (2007-01-26). "Strong relationship between DMS and the solar radiation dose over the global surface ocean". Science. 315 (5811): 506–508. Bibcode:2007Sci...315..506V. doi:10.1126/science.1133680. PMID 17255509. Retrieved 2008-03-21.
  • Vila-Costa, M.; et al. (2006-10-27). "Dimethylsulfoniopropionate uptake by marine phytoplankton". Science. 314 (5799): 652–654. Bibcode:2006Sci...314..652V. doi:10.1126/science.1131043. PMID 17068265. Retrieved 2008-03-21.
  • Volkman, J. K.; S. M. Barrerr; S. I. Blackburn; E. L. Sikes (1995). "Alkenones in Gephyrocapsa oceanica: Implications for studies of paleoclimate". Geochimica et Cosmochimica Acta. 59 (3): 513–520. Bibcode:1995GeCoA..59..513V. doi:10.1016/0016-7037(95)00325-T.

External links

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