Gephyrocapsa huxleyi

Last updated

Gephyrocapsa huxleyi
Emiliania huxleyi.jpg
A scanning electron micrograph of a single G. huxleyi cell
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Clade: Diaphoretickes
Phylum: Haptista
Subphylum: Haptophytina
Class: Coccolithophyceae
Order: Isochrysidales
Family: Noelaerhabdaceae
Genus: Gephyrocapsa
Species:
G. huxleyi
Binomial name
Gephyrocapsa huxleyi
Synonyms [2] [3]
Bloom of E. huxleyi in Hardangerfjord, Norway, May 2020 Hardangerfjord bloom 2020.jpg
Bloom of E. huxleyi in Hardangerfjord, Norway, May 2020

Gephyrocapsa huxleyi, formerly called Emiliania huxleyi, is a species of coccolithophore found in almost all ocean ecosystems from the equator to sub-polar regions, and from nutrient rich upwelling zones to nutrient poor oligotrophic waters. [4] [5] [6] [7] It is one of thousands of different photosynthetic plankton that freely drift in the photic 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. 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.

Contents

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 believed to have evolved approximately 270,000 years ago from the older genus Gephyrocapsa Kampter [8] [9] and became dominant in planktonic assemblages, and thus in the fossil record, approximately 70,000 years ago. [8] [10] It is the most numerically abundant and widespread coccolithophore species. The species is divided into seven morphological forms called morphotypes based on differences in coccolith structure [11] [12] [13] (See Nannotax for more detail on these forms). 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 areas of more than 10,000 km, with complementary shipboard measurements indicating that E. huxleyi is by far the dominant phytoplankton species under these conditions. [14] 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.[ citation needed ]

Abundance and distribution

Emiliania huxleyi is considered a ubiquitous species. It exhibits one of the largest temperature ranges (1–30 °C) of any coccolithophores species. [6] It has been observed under a range of nutrient levels from oligotrophic (subtropical gyres) to eutrophic waters (upwelling zones/ Norwegian fjords). [15] [16] [17] Its presence in plankton communities from the surface to 200m depth indicates a high tolerance for both fluctuating and low light conditions. [7] [15] [18] This extremely wide tolerance of environmental conditions is believed to be explained by the existence of a range of environmentally adapted ecotypes within the species. [9] As a result of these tolerances its distribution ranges from the sub-Arctic to the sub-Antarctic and from coastal to oceanic habitats. [6] [19] Within this range it is present in nearly all euphotic zone water samples and accounts for 20–50% or more of the total coccolithophore community. [6] [15] [20] [21]

During massive blooms (which can cover over 100,000 square kilometers), E. huxleyi 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. [14] E. huxleyi 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. [22] 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 E. huxleyi 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, E. huxleyi has inspired proposals for geomimesis, [23] 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 E. huxleyi 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 E. huxleyi, 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 yet well understood.

Ocean heat retention

Scattering stimulated by E. huxleyi 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 E. huxleyi 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. Reinhardt, P. (1972). Coccolithen. Kalkiges Plankton seit Jahrmillionen. Die neue Brehm Bücheri Vol. 453. pp. 1–99, 188 figures. Wittenberg Lutherstadt: A. Ziemsen Verlag
  2. M.D. Guiry in Guiry, M.D. & Guiry, G.M. 15 November 2023. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. https://www.algaebase.org/search/species/detail/?species_id=70636  ; searched on 16 June 2024
  3. Guiry, M.D. & Guiry, G.M. (2024). AlgaeBase. World-wide electronic publication, National University of Ireland, Galway (taxonomic information republished from AlgaeBase with permission of M.D. Guiry). Gephyrocapsa huxleyi (Lohmann) P.Reinhardt, 1972. Accessed through: World Register of Marine Species at: https://www.marinespecies.org/aphia.php?p=taxdetails&id=236056 Archived 4 August 2023 at the Wayback Machine on 16 June 2024
  4. Okada, Hisatake (1973). "The distribution of oceanic coccolithophorids in the Pacific". Deep Sea Research and Oceanographic Abstracts. 20 (4): 355–374. Bibcode:1973DSRA...20..355O. doi:10.1016/0011-7471(73)90059-4.
  5. Charalampopoulou, Anastasia (2011) Coccolithophores in high latitude and Polar regions: Relationships between community composition, calcification and environmental factors University of Southampton, School of Ocean and Earth Science, Doctoral Thesis, 139pp.
  6. 1 2 3 4 McIntyre, Andrew (1967). "Modern coccolithophoridae of the atlantic ocean—I. Placoliths and cyrtoliths". Deep Sea Research and Oceanographic Abstracts. 14 (5): 561–597. Bibcode:1967DSRA...14..561M. doi:10.1016/0011-7471(67)90065-4.
  7. 1 2 Boeckel, Babette; Baumann, Karl-Heinz (1 May 2008). "Vertical and lateral variations in coccolithophore community structure across the subtropical frontal zone in the South Atlantic Ocean". Marine Micropaleontology. 67 (3–4): 255–273. Bibcode:2008MarMP..67..255B. doi:10.1016/j.marmicro.2008.01.014.
  8. 1 2 Thierstein, H. R.; Geitzenauer, K. R.; Molfino, B.; Shackleton, N. J. (1 July 1977). "Global synchroneity of late Quaternary coccolith datum levels Validation by oxygen isotopes". Geology. 5 (7): 400–404. Bibcode:1977Geo.....5..400T. doi:10.1130/0091-7613(1977)5<400:gsolqc>2.0.co;2. ISSN   0091-7613.
  9. 1 2 Paasche, E. (2001). "A review of the coccolithophorid Emiliania huxleyi (Prymnesiophyceae), with particular reference to growth, coccolith formation, and calcification-photosynthesis interactions". Phycologia. 40 (6): 503–529. doi:10.2216/i0031-8884-40-6-503.1. S2CID   84921998.
  10. Bijma, J.; et al. (2001). "Primary signal: Ecological and environmental factors—Report from Working Group 2" (PDF). Geochemistry, Geophysics, Geosystems. 2 (1): n/a. Bibcode:2001GGG.....2.1003B. doi: 10.1029/2000gc000051 . Archived (PDF) from the original on 28 November 2020. Retrieved 25 September 2019.
  11. Findlay, C. S; Giraudeau, J (1 December 2000). "Extant calcareous nannoplankton in the Australian Sector of the Southern Ocean (austral summers 1994 and 1995)". Marine Micropaleontology. 40 (4): 417–439. Bibcode:2000MarMP..40..417F. doi:10.1016/S0377-8398(00)00046-3.
  12. Cook, S.S.; et al. (2011). "Photosynthetic pigment and genetic differences between two Southern Ocean morphotypes of Emiliania Huxleyi (Haptophyta)". Journal of Phycology. 47 (3): 615–626. doi:10.1111/j.1529-8817.2011.00992.x. PMID   27021991. S2CID   25399383.
  13. Hagino, Kyoko; Bendif, El Mahdi; Young, Jeremy R.; Kogame, Kazuhiro; Probert, Ian; Takano, Yoshihito; Horiguchi, Takeo; de Vargas, Colomban; Okada, Hisatake (13 October 2011). "NEW EVIDENCE FOR MORPHOLOGICAL AND GENETIC VARIATION IN THE COSMOPOLITAN COCCOLITHOPHORE EMILIANIA HUXLEYI (PRYMNESIOPHYCEAE) FROM THE COX1b ‐ ATP4 GENES 1". Journal of Phycology. 47 (5): 1164–1176. doi:10.1111/j.1529-8817.2011.01053.x. ISSN   0022-3646.
  14. 1 2 Holligan, P. M.; et al. (1993). "A biogeochemical study of the coccolithophore, Emiliania huxleyi, in the North Atlantic". Global Biogeochem. Cycles. 7 (4): 879–900. Bibcode:1993GBioC...7..879H. doi:10.1029/93GB01731.
  15. 1 2 3 Winter, A., Jordan, R.W. & Roth, P.H., 1994. Biogeography of living coccolithophores in ocean waters. In Coccolithophores. Cambridge, United Kingdom: Cambridge University Press, pp. 161–177.
  16. Hagino, Kyoko; Okada, Hisatake (30 January 2006). "Intra- and infra-specific morphological variation in selected coccolithophore species in the equatorial and subequatorial Pacific Ocean" (PDF). Marine Micropaleontology. 58 (3): 184–206. Bibcode:2006MarMP..58..184H. doi:10.1016/j.marmicro.2005.11.001. hdl: 2115/5820 . Archived (PDF) from the original on 23 September 2019. Retrieved 23 September 2019.
  17. Henderiks, J; Winter, A; Elbrächter, M; Feistel, R; Plas, Av der; Nausch, G; Barlow, R (23 February 2012). "Environmental controls on Emiliania huxleyi morphotypes in the Benguela coastal upwelling system (SE Atlantic)". Marine Ecology Progress Series. 448: 51–66. Bibcode:2012MEPS..448...51H. doi: 10.3354/meps09535 . ISSN   0171-8630.
  18. Mohan, Rahul; Mergulhao, Lina P.; Guptha, M. V. S.; Rajakumar, A.; Thamban, M.; AnilKumar, N.; Sudhakar, M.; Ravindra, Rasik (1 April 2008). "Ecology of coccolithophores in the Indian sector of the Southern Ocean". Marine Micropaleontology. 67 (1–2): 30–45. Bibcode:2008MarMP..67...30M. doi:10.1016/j.marmicro.2007.08.005.
  19. Hasle, G.R., 1969. An analysis of the phytoplankton of the Pacific Southern Ocean: Abundance, composition, and distribution during the Brategg Expedition, 1947–1948, Universitetsforlaget.
  20. Beaufort, L.; Couapel, M.; Buchet, N.; Claustre, H.; Goyet, C. (4 August 2008). "Calcite production by coccolithophores in the south east Pacific Ocean". Biogeosciences. 5 (4): 1101–1117. Bibcode:2008BGeo....5.1101B. doi: 10.5194/bg-5-1101-2008 . ISSN   1726-4189.
  21. Poulton, A.J.; et al. (2010). "Coccolithophore dynamics in non-bloom conditions during late summer in the central Iceland Basin (July–August 2007)" (PDF). Limnology and Oceanography. 55 (4): 1601–1613. Bibcode:2010LimOc..55.1601P. doi:10.4319/lo.2010.55.4.1601. S2CID   53312384. Archived (PDF) from the original on 11 April 2021. Retrieved 1 July 2019.
  22. Westbroek, Peter (1993). "A model system approach to biological climate forcing. The example of Emiliania huxleyi". Global and Planetary Change. 8 (1–2): 27–46. Bibcode:1993GPC.....8...27W. doi:10.1016/0921-8181(93)90061-R.
  23. Seitz, R (2011). "Bright water: Hydrosols, water conservation, and climate change". Climatic Change. 105 (3–4): 365–381. arXiv: 1010.5823 . Bibcode:2011ClCh..105..365S. doi:10.1007/s10584-010-9965-8. S2CID   16243560.

Related Research Articles

<span class="mw-page-title-main">Coccolithophore</span> Unicellular algae responsible for the formation of chalk

Coccolithophores, or coccolithophorids, are single-celled organisms which are part of the phytoplankton, the autotrophic (self-feeding) component of the plankton community. They form a group of about 200 species, and belong either to the kingdom Protista, according to Robert Whittaker's five-kingdom system, or clade Hacrobia, according to a newer biological classification system. Within the Hacrobia, the coccolithophores are in the phylum or division Haptophyta, class Prymnesiophyceae. Coccolithophores are almost exclusively marine, are photosynthetic and mixotrophic, and exist in large numbers throughout the sunlight zone of the ocean.

<span class="mw-page-title-main">Haptophyte</span> Type of algae

The haptophytes, classified either as the Haptophyta, Haptophytina or Prymnesiophyta, are a clade of algae.

<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 πλαγκτός, meaning 'wanderer' or 'drifter'.

<span class="mw-page-title-main">Biological pump</span> Carbon capture process in oceans

The biological pump (or ocean carbon biological pump or marine biological carbon pump) is the ocean's biologically driven sequestration of carbon from the atmosphere and land runoff to the ocean interior and seafloor sediments. In other words, it is a biologically mediated process which results in the sequestering of carbon in the deep ocean away from the atmosphere and the land. The biological pump is the biological component of the "marine carbon pump" which contains both a physical and biological component. It is the part of the broader oceanic carbon cycle responsible for the cycling of organic matter formed mainly by phytoplankton during photosynthesis (soft-tissue pump), as well as the cycling of calcium carbonate (CaCO3) formed into shells by certain organisms such as plankton and mollusks (carbonate pump).

<span class="mw-page-title-main">Coccolith</span> Calcium carbonate scales covering some phytoplankton species

Coccoliths are individual plates or scales of calcium carbonate formed by coccolithophores and cover the cell surface arranged in the form of a spherical shell, called a coccosphere.

<span class="mw-page-title-main">Dimethylsulfoniopropionate</span> Chemical compound

Dimethylsulfoniopropionate (DMSP), is an organosulfur compound with the formula (CH3)2S+CH2CH2COO. This zwitterionic metabolite can be found in marine phytoplankton, seaweeds, and some species of terrestrial and aquatic vascular plants. It functions as an osmolyte as well as several other physiological and environmental roles have also been identified. DMSP was first identified in the marine red alga Polysiphonia fastigiata.

Alkenones are long-chain unsaturated methyl and ethyl n-ketones produced by a few phytoplankton species of the class Prymnesiophyceae. Alkenones typically contain between 35 and 41 carbon atoms and with between two and four double bonds. Uniquely for biolipids, alkenones have a spacing of five methylene groups between double bonds, which are of the less common E configuration. The biological function of alkenones remains under debate although it is likely that they are storage lipids. Alkenones were first described in ocean sediments recovered from Walvis Ridge and then shortly afterwards in cultures of the marine coccolithophore Gephyrocapsa huxleyi. The earliest known occurrence of alkenones is during the Aptian 120 million years ago. They are used in organic geochemistry as a proxy for past sea surface temperature.

Phycodnaviridae is a family of large (100–560 kb) double-stranded DNA viruses that infect marine or freshwater eukaryotic algae. Viruses within this family have a similar morphology, with an icosahedral capsid. As of 2014, there were 33 species in this family, divided among 6 genera. This family belongs to a super-group of large viruses known as nucleocytoplasmic large DNA viruses. Evidence was published in 2014 suggesting that specific strains of Phycodnaviridae might infect humans rather than just algal species, as was previously believed. Most genera under this family enter the host cell by cell receptor endocytosis and replicate in the nucleus. Phycodnaviridae play important ecological roles by regulating the growth and productivity of their algal hosts. Algal species such Heterosigma akashiwo and the genus Chrysochromulina can form dense blooms which can be damaging to fisheries, resulting in losses in the aquaculture industry. Heterosigma akashiwo virus (HaV) has been suggested for use as a microbial agent to prevent the recurrence of toxic red tides produced by this algal species. Phycodnaviridae cause death and lysis of freshwater and marine algal species, liberating organic carbon, nitrogen and phosphorus into the water, providing nutrients for the microbial loop.

<i>Emiliania</i> (coccolithophore) Genus of single-celled organisms

Emiliania is a global coccolithophorid genus.

<i>Gephyrocapsa oceanica</i> Species of single-celled organism

Gephyrocapsa oceanica is a species of coccolithophorid. It is the type species of the genus Gephyrocapsa. The species is an important Pleistocene biostratigraphic marker.

<span class="mw-page-title-main">Marine biogenic calcification</span> Shell formation mechanism

Marine biogenic calcification is the production of calcium carbonate by organisms in the global ocean.

Rappephyceae, or Rappemonads, are a small family of protists first described in 2011, of uncertain phylogenic affinity. It has been discussed as a possible member of a larger clade Haptophyta. This newly identified taxonomic class of phytoplankton are named after a professor from the Hawai’i institute of marine biology, known as Michael Rappé. Rappé discovered these phytoplankton in the Atlantic Ocean and published his findings on their DNA in 1998. Current research has shown that these organisms provide an immense amount of nutritional molecules, such as oxygen, for other organisms using biochemical processes like photosynthesis and carbon fixation.

<span class="mw-page-title-main">Marine primary production</span> Marine synthesis of organic compounds

Marine primary production is the chemical synthesis in the ocean of organic compounds from atmospheric or dissolved carbon dioxide. It principally occurs through the process of photosynthesis, which uses light as its source of energy, but it also occurs through chemosynthesis, which uses the oxidation or reduction of inorganic chemical compounds as its source of energy. Almost all life on Earth relies directly or indirectly on primary production. The organisms responsible for primary production are called primary producers or autotrophs.

<span class="mw-page-title-main">Marine protists</span> Protists that live in saltwater or brackish water

Marine protists are defined by their habitat as protists that live in marine environments, that is, in the saltwater of seas or oceans or the brackish water of coastal estuaries. Life originated as marine single-celled prokaryotes and later evolved into more complex eukaryotes. Eukaryotes are the more developed life forms known as plants, animals, fungi and protists. Protists are the eukaryotes that cannot be classified as plants, fungi or animals. They are mostly single-celled and microscopic. The term protist came into use historically as a term of convenience for eukaryotes that cannot be strictly classified as plants, animals or fungi. They are not a part of modern cladistics because they are paraphyletic.

<span class="mw-page-title-main">Protist shell</span> Protective shell of a type of eukaryotic organism

Many protists have protective shells or tests, usually made from silica (glass) or calcium carbonate (chalk). Protists are a diverse group of eukaryote organisms that are not plants, animals, or fungi. They are typically microscopic unicellular organisms that live in water or moist environments.

<span class="mw-page-title-main">Particulate inorganic carbon</span>

Particulate inorganic carbon (PIC) can be contrasted with dissolved inorganic carbon (DIC), the other form of inorganic carbon found in the ocean. These distinctions are important in chemical oceanography. Particulate inorganic carbon is sometimes called suspended inorganic carbon. In operational terms, it is defined as the inorganic carbon in particulate form that is too large to pass through the filter used to separate dissolved inorganic carbon.

<span class="mw-page-title-main">Great Calcite Belt</span> High-calcite region of the Southern Ocean

The Great Calcite Belt (GCB) refers to a region of the ocean where there are high concentrations of calcite, a mineral form of calcium carbonate. The belt extends over a large area of the Southern Ocean surrounding Antarctica. The calcite in the Great Calcite Belt is formed by tiny marine organisms called coccolithophores, which build their shells out of calcium carbonate. When these organisms die, their shells sink to the bottom of the ocean, and over time, they accumulate to form a thick layer of calcite sediment.

Linda Karen Medlin is a molecular biologist known for her work on diatoms. She is an elected member of the Norwegian Academy of Science and Letters.

Ana María Gayoso was an Argentine marine biologist, a specialist in study of marine phytoplankton, best known for being the first scientist to describe phytoplankton in the Bahía Blanca Estuary, and to initiate the sustained long-term oceanographic dataset in this ecosystem. She made significant contributions to the understanding of harmful algal blooms caused by toxic dinoflagellate species in the Patagonian gulfs, and was the first scientist to describe high abundances of the coccolithophore Emiliania huxleyi in the Argentine Sea, a key component in the primary productivity along the Patagonian Shelf Break front in the SW South Atlantic. She started the most extensive (1978-present) long-term database of phytoplankton and physico-chemical variables in South America, in a fixed monitoring site in the Bahía Blanca Estuary. She died on 28 December 2004 in Puerto Madryn.

Maureen Hatcher Conte is biogeochemist known for her work using particles to define the long-term cycling of chemical compounds in seawater.

References