Emiliania huxleyi

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Emiliania huxleyi
A scanning electron micrograph of a single Emiliania huxleyi cell.
Scientific classification
Domain:
Eukaryota
(unranked):
Haptophyta
Class:
Prymnesiophyceae
Order:
Isochrysidales
Family:
Noelaerhabdaceae
Genus:
Emiliania
Species:
E. huxleyi
Binomial name
Emiliania huxleyi
(Lohm.) Hay and Mohler
Bloom of E. huxleyi in Hardangerfjord, Norway, May 2020

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.[1][2][3][4] 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.

Basic facts

Emiliania huxleyi was named after

morphotypes based on differences in coccolith structure[8][9][10] (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.[11] 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.

eutrophic waters (upwelling zones/ Norwegian fjords).[12][13][14] Its presence in plankton communities from the surface to 200m depth indicates a high tolerance for both fluctuating and low light conditions.[4][12][15] 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.[6] As a result of these tolerances its distribution ranges from the sub-Arctic to the sub-Antarctic and from coastal to oceanic habitats.[3][16] 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.[3][12][17][18]

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.[11] 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.[19] 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,[20] 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.

Gallery

  • Landsat image of a 1999 E. huxleyi bloom in the English Channel.
    Landsat
    image of a 1999 E. huxleyi bloom in the English Channel.
  • E. huxleyi bloom in the Barents Sea.
    E. huxleyi bloom in the Barents Sea.

See also

Notes

  1. doi:10.1016/0011-7471(73)90059-4
    .
  2. ^ 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.
  3. ^
    doi:10.1016/0011-7471(67)90065-4
    .
  4. ^
    doi:10.1016/j.marmicro.2008.01.014
    .
  5. ^
    ISSN 0091-7613
    .
  6. ^
    S2CID 84921998
    .
  7. doi:10.1029/2000gc000051
    .
  8. doi:10.1016/S0377-8398(00)00046-3
    .
  9. S2CID 25399383
    .
  10. S2CID 24499896.[permanent dead link
    ]
  11. ^
    doi:10.1029/93GB01731
    .
  12. ^ a b c 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.
  13. hdl:2115/5820
    .
  14. ISSN 0171-8630
    .
  15. doi:10.1016/j.marmicro.2007.08.005
    .
  16. ^ 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.
  17. ISSN 1726-4189
    .
  18. S2CID 53312384
    .
  19. doi:10.1016/0921-8181(93)90061-R
    .
  20. S2CID 16243560
    .

References

External links
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