Foraminifera

Foraminifera
Temporal range: Cambrian–Recent
Live Ammonia tepida (Rotaliida)
Scientific classification
Domain: Eukaryota
(unranked): SAR
(unranked): Rhizaria
Phylum: Retaria
Subphylum: Foraminifera
Orders

Allogromiida
Carterinida
Fusulinida — extinct
Globigerinida
Involutinida — extinct
Lagenida
Miliolida
Robertinida
Rotaliida
Silicoloculinida
Spirillinida
Textulariida
incertae sedis
   Xenophyophorea
   Reticulomyxa

Foraminifera (/fəˌræməˈnɪfərə/, Latin meaning hole bearers, informally called "forams") are members of a phylum or class of amoeboid protists characterized by streaming granular ectoplasm that among other things is used for catching food, and commonly by an external shell or "test" made of various materials and constructed in diverse forms. All but perhaps a very few are aquatic and most are marine, the majority of which live on or within the seafloor sediment (i.e., are benthic) while a smaller variety are floaters in the water column at various depths (i.e., are planktonic). A few are known from freshwater or brackish conditions and some soil species have been identified through molecular analysis of small subunit ribosomal DNA.[1][2]

Foraminifera typically produce a test, or shell, which can have either one or multiple chambers, some becoming quite elaborate in structure.[3] These shells are commonly made of calcium carbonate (CaCO
3) or agglutinated sediment particles. Over 50,000 species are recognized, both living (10,000)[4] and fossil (40,000).[5][6] They are usually less than 1 mm in size, but some are much larger, the largest species reaching up to 20 cm.[7]

The word foraminifera is the Latin plural of the singular noun foraminifer, which is also used in English to refer to single individuals of the class Foraminifera. Alternatively, the English adjective "foraminiferan" can be used as a noun to refer to such individuals.

Taxonomy

The taxonomic position of the Foraminifera has varied since their recognition as protozoa (protists) by Schultze in 1854,[8] there referred to as an order, Foraminiferida. Loeblich and Tappan (1992) reranked Foraminifera as a class[9] as it is now commonly regarded.

The Foraminifera have typically been included in the Protozoa,[10][11][12] or in the similar Protoctista or Protist kingdom.[13][14] Compelling evidence, based primarily on molecular phylogenetics, exists for their belonging to a major group within the Protozoa known as the Rhizaria.[10] Prior to the recognition of evolutionary relationships among the members of the Rhizaria, the Foraminifera were generally grouped with other amoeboids as phylum Rhizopodea (or Sarcodina) in the class Granuloreticulosa.

The Rhizaria are problematic, as they are often called a "supergroup", rather than using an established taxonomic rank such as phylum. Cavalier-Smith defines the Rhizaria as an infrakingdom within the kingdom Protozoa.[10]

Some taxonomies put the Foraminifera in a phylum of their own, putting them on par with the amoeboid Sarcodina in which they had been placed.

Although as yet unsupported by morphological correlates, molecular data strongly suggest the Foraminifera are closely related to the Cercozoa and Radiolaria, both of which also include amoeboids with complex shells; these three groups make up the Rhizaria.[11] However, the exact relationships of the forams to the other groups and to one another are still not entirely clear. Foraminifera are closely related to testate amoebae.[15]

Living Foraminifera

Modern Foraminifera are primarily marine organisms, but living individuals have been found in brackish, freshwater [16] and even terrestrial habitats.[2] The majority of the species are benthic, and a further 40 morphospecies are planktonic.[17] This count may, however, represent only a fraction of actual diversity, since many genetically discrepant species may be morphologically indistinguishable.[18]

A number of forams have unicellular algae as endosymbionts, from diverse lineages such as the green algae, red algae, golden algae, diatoms, and dinoflagellates.[17] Some forams are kleptoplastic, retaining chloroplasts from ingested algae to conduct photosynthesis.[19]

Biology

The foraminiferal cell is divided into granular endoplasm and transparent ectoplasm from which a pseudopodial net may emerge through a single opening or through many perforations in the test. Individual pseudopods characteristically have small granules streaming in both directions.[16] The pseudopods are used for locomotion, anchoring, and in capturing food, which consists of small organisms such as diatoms or bacteria.[17]

The foraminiferal life-cycle involves an alternation between haploid and diploid generations, although they are mostly similar in form.[8][20] The haploid or gamont initially has a single nucleus, and divides to produce numerous gametes, which typically have two flagella. The diploid or schizont is multinucleate, and after meiosis fragments to produce new gamonts. Multiple rounds of asexual reproduction between sexual generations is not uncommon in benthic forms.[16]

Abundance of certain Foraminifera is sometimes used by researchers as an indicator of the completeness of vertical mixing in certain seas such as the Celtic Sea.

Tests

Foraminiferan tests (ventral view)
Fossil nummulitid foraminiferans showing microspheric and megalospheric individuals; Eocene of the United Arab Emirates; scale in mm.
The miliolid foraminiferan Quinqueloculina from the Belgian part of the North Sea.
Thin section of a peneroplid foraminiferan from Holocene lagoonal sediment in Rice Bay, San Salvador Island, Bahamas. Scale bar 100 micrometres.
Ammonia beccarii, a benthic foram from the North Sea.
Foraminifera Baculogypsina sphaerulata of Hatoma Island, Japan. Field width = 5.22 mm.

The form and composition of their tests are the primary means by which forams are identified and classified. Most have calcareous tests, composed of calcium carbonate.[16] In other forams, the tests may be composed of organic material, made from small pieces of sediment cemented together (agglutinated), and in one genus, of silica. Openings in the test, including those that allow cytoplasm to flow between chambers, are called apertures. The test contains an organic matrix, which can sometimes be recovered from fossil samples.[21]

Tests are known as fossils as far back as the Cambrian period,[22] and many marine sediments are composed primarily of them. For instance, the limestone that makes up the pyramids of Egypt is composed almost entirely of nummulitic benthic Foraminifera.[23] Production estimates indicate that reef Foraminifera annually generate about 43 million tons of calcium carbonate per year, thus play an essential role in the production of reef carbonates.[24]

Genetic studies have identified the naked amoeba "Reticulomyxa" and the peculiar xenophyophores as foraminiferans without tests. A few other amoeboids produce reticulose pseudopods, and were formerly classified with the forams as the Granuloreticulosa, but this is no longer considered a natural group, and most are now placed among the Cercozoa.[25]

Deep-sea species

Foraminifera are found in the deepest parts of the ocean such as the Mariana Trench, including the Challenger Deep, the deepest part known. At these depths, below the carbonate compensation depth, the calcium carbonate of the tests is soluble in water due to the extreme pressure. The Foraminifera found in the Challenger Deep thus have no carbonate test, but instead have one of organic material.[26]

Four species found in the Challenger Deep are unknown from any other place in the oceans, one of which is representative of an endemic genus unique to the region. They are Resigella laevis and R. bilocularis, Nodellum aculeata, and Conicotheca nigrans (the unique genus). All have tests that are mainly of transparent organic material which have small (about 100 nm) plates that appear to be clay.[26]

Evolutionary significance

Dying planktonic Foraminifera continuously rain down on the sea floor in vast numbers, their mineralized tests preserved as fossils in the accumulating sediment. Beginning in the 1960s, and largely under the auspices of the Deep Sea Drilling, Ocean Drilling, and International Ocean Drilling Programmes, as well as for the purposes of oil exploration, advanced deep-sea drilling techniques have been bringing up sediment cores bearing Foraminifera fossils.[27] The effectively unlimited supply of these fossil tests and the relatively high-precision age-control models available for cores has produced an exceptionally high-quality planktonic Foraminifera fossil record dating back to the mid-Jurassic, and presents an unparalleled record for scientists testing and documenting the evolutionary process.[27] The exceptional quality of the fossil record has allowed an impressively detailed picture of species inter-relationships to be developed on the basis of fossils, in many cases subsequently validated independently through molecular genetic studies on extant specimens[28] Larger benthic Foraminifera with complex shell structure react in a highly specific manner to the different benthic environments and, therefore, the composition of the assemblages and the distribution patterns of particular species reflect simultaneously bottom types and the light gradient. In the course of Earth history, larger Foraminifera are replaced frequently. In particular, associations of Foraminifera characterizing particular shallow water facies types are dying out and are replaced after a certain time interval by new associations with the same structure of shell morphology, emerging from a new evolutionary process of adaptation. These evolutionary processes make the larger Foraminifera useful as index fossils for the Permian, Jurassic, Cretaceous and Cenozoic.

Uses

Because of their diversity, abundance, and complex morphology, fossil foraminiferal assemblages are useful for biostratigraphy, and can accurately give relative dates to sedimentary rocks. The oil industry relies heavily on microfossils such as forams to find potential hydrocarbon deposits.[29]

Calcareous fossil Foraminifera are formed from elements found in the ancient seas where they lived. Thus, they are very useful in paleoclimatology and paleoceanography. They can be used to reconstruct past climate by examining the stable isotope ratios and trace element content of the shells (tests). Global temperature and ice volume can be revealed by the isotopes of oxygen, and the history of the carbon cycle and oceanic productivity by examining the stable isotope ratios of carbon;[30] see δ18O and δ13C. The concentration of trace elements, like magnesium (Mg),[31] lithium (Li)[32] and boron (B),[33] also hold a wealth of information about global temperature cycles, continental weathering, and the role of the ocean in the global carbon cycle. Geographic patterns seen in the fossil records of planktonic forams are also used to reconstruct ancient ocean currents. Because certain types of Foraminifera are found only in certain environments, they can be used to figure out the kind of environment under which ancient marine sediments were deposited.

For the same reasons they make useful biostratigraphic markers, living foraminiferal assemblages have been used as bioindicators in coastal environments, including indicators of coral reef health. Because calcium carbonate is susceptible to dissolution in acidic conditions, Foraminifera may be particularly affected by changing climate and ocean acidification.

Foraminifera have many uses in petroleum exploration and are used routinely to interpret the ages and paleoenvironments of sedimentary strata in oil wells.[34] Agglutinated fossil Foraminifera buried deeply in sedimentary basins can be used to estimate thermal maturity, which is a key factor for petroleum generation. The Foraminiferal Colouration Index [35] (FCI) is used to quantify colour changes and estimate burial temperature. FCI data is particularly useful in the early stages of petroleum generation (about 100 °C).

Foraminifera can also be used in archaeology in the provenancing of some stone raw material types. Some stone types, such as limestone, are commonly found to contain fossilised Foraminifera. The types and concentrations of these fossils within a sample of stone can be used to match that sample to a source known to contain the same "fossil signature".

Gallery

References

  1. ↑ Giere, Olav (2009). Meiobenthology: the microscopic motile fauna of aquatic sediments (2nd ed.). Berlin: Springer. ISBN 978-3540686576.
  2. 1 2 Lejzerowicz, Franck; Pawlowski, Jan; Fraissinet-Tachet, Laurence; Marmeisse, Roland (1 September 2010). "Molecular evidence for widespread occurrence of Foraminifera in soils". Environmental Microbiology. 12 (9): 2518–26. doi:10.1111/j.1462-2920.2010.02225.x. PMID 20406290.
  3. ↑ Kennett, J.P.; Srinivasan, M.S. (1983). Neogene planktonic foraminifera: a phylogenetic atlas. Hutchinson Ross. ISBN 978-0-87933-070-5.
  4. ↑ Ald, S.M. et al. (2007) Diversity, Nomenclature, and Taxonomy of Protists, Syst. Biol. 56(4), 684–689, DOI: 10.1080/10635150701494127.
  5. ↑ Pawlowski, J., Lejzerowicz, F., & Esling, P. (2014). Next-generation environmental diversity surveys of foraminifera: preparing the future. The Biological Bulletin, 227(2), 93-106.
  6. ↑ "World Foraminifera Database".
  7. ↑ Marshall M (3 February 2010). "Zoologger: 'Living beach ball' is giant single cell". New Scientist.
  8. 1 2 Loeblich Jr, A.R.; Tappan, H. (1964). "Foraminiferida". Part C, Protista 2. Treatise on Invertebrate Paleontology. Geological Society of America. pp. C55–C786. ISBN 0-8137-3003-1.
  9. ↑ Sen Gupta, Barun K. (2002). Modern Foraminifera. Springer. p. 16. ISBN 978-1-4020-0598-5.
  10. 1 2 3 Cavalier-Smith, T (2004). "Only Six Kingdoms of Life" (PDF).
  11. 1 2 Cavalier-Smith, T (2003). "Protist phylogeny and the high-level classification of Protozoa". European Journal of Protistology. 34 (4): 338–348. doi:10.1078/0932-4739-00002.
  12. ↑ Tolweb Cercozoa
  13. ↑ European Register of Marine Species
  14. ↑ eForams-taxonomy
  15. ↑ Testate amoebae as environmental indicators (PDF)
  16. 1 2 3 4 Sen Gupta, Barun K. (1982). "Ecology of benthic Foraminifera". In Broadhead, T.W. Foraminifera: notes for a short course organized by M.A. Buzas and B.K. Sen Gupta. Studies in Geology. 6. University of Tennessee, Dept. of Geological Sciences. pp. 37–50. ISBN 0910249059. OCLC 9276403.
  17. 1 2 3 Hemleben, C.; Anderson, O.R.; Spindler, M. (1989). Modern Planktonic Foraminifera. Springer-Verlag. ISBN 978-3-540-96815-3.
  18. ↑ Kucera, M.; Darling, K.F. (April 2002). "Cryptic species of planktonic foraminifera: their effect on palaeoceanographic reconstructions". Philos Trans A Math Phys Eng Sci. 360 (1793): 695–718. Bibcode:2002RSPTA.360..695K. doi:10.1098/rsta.2001.0962. PMID 12804300.
  19. ↑ Bernhard, J. M.; Bowser, S.M. (1999). "Benthic Foraminifera of dysoxic sediments: chloroplast sequestration and functional morphology". Earth Science Reviews. 46: 149–165. Bibcode:1999ESRv...46..149B. doi:10.1016/S0012-8252(99)00017-3.
  20. ↑ Moore, R.C.; Lalicker, A.G.; Fischer, C.G. (1952). "Ch 2 Foraminifera and Radiolaria". Invertebrate Fossils. McGraw-Hill. OCLC 547380.
  21. ↑ Lana, C (2001). "Cretaceous Carterina (Foraminifera)". Marine Micropaleontology. 41: 97. doi:10.1016/S0377-8398(00)00050-5.
  22. ↑ Dartnell L (8 May 2008). "Sea creatures had a thing for bling". New Scientist (2655).
  23. ↑ Foraminifera: History of Study, University College London, retrieved 20 September 2007
  24. ↑ Langer, M. R.; Silk, M. T. B.; Lipps, J. H. (1997). "Global ocean carbonate and carbon dioxide production: The role of reef Foraminifera". Journal of Foraminiferal Research. 27 (4): 271–277. doi:10.2113/gsjfr.27.4.271.
  25. ↑ Adl, S. M.; Simpson, A. G. B.; Farmer, M. A.; Anderson; et al. (2005). "The new higher level classification of Eukaryotes with emphasis on the taxonomy of Protists". Journal of Eukaryotic Microbiology. 52 (5): 399–451. doi:10.1111/j.1550-7408.2005.00053.x. PMID 16248873.
  26. 1 2 Gooday, A.J.; Todo, Y.; Uematsu, K.; Kitazato, H. (July 2008). "New organic-walled Foraminifera (Protista) from the ocean's deepest point, the Challenger Deep (western Pacific Ocean)". Zoological Journal of the Linnean Society. 153 (3): 399–423. doi:10.1111/j.1096-3642.2008.00393.x.
  27. 1 2 http://www.nature.com/nature/debates/fossil/fossil_1.html
  28. ↑ Journal bioinformatics and biology insights, Using the Multiple Analysis Approach to Reconstruct Phylogenetic Relationships among Planktonic Foraminifera from Highly Divergent and Length-polymorphic SSU rDNA Sequences
  29. ↑ Boardman, R.S.; Cheetham, A.H.; Rowell, A.J. (1987). Fossil Invertebrates. Wiley. ISBN 0865423024.
  30. ↑ Zachos, J.C.; Pagani, M.; Sloan, L.; Thomas, E.; Billups, K. (2001). "Trends, Rhythms, and Aberrations in Global Climate, 65 Ma to Present". Science. 292 (5517): 686–693. Bibcode:2001Sci...292..686Z. doi:10.1126/science.1059412. PMID 11326091.
  31. ↑ Branson, Oscar; Redfern, Simon A.T.; Tyliszczak, Tolek; Sadekov, Aleksey; Langer, Gerald; Kimoto, Katsunori; Elderfield, Henry (December 2013). "The coordination of Mg in foraminiferal calcite". Earth and Planetary Science Letters. 383: 134–141. Bibcode:2013E&PSL.383..134B. doi:10.1016/j.epsl.2013.09.037.
  32. ↑ Misra, S.; Froelich, P. N. (26 January 2012). "Lithium Isotope History of Cenozoic Seawater: Changes in Silicate Weathering and Reverse Weathering". Science. 335 (6070): 818–823. Bibcode:2012Sci...335..818M. doi:10.1126/science.1214697. PMID 22282473.
  33. ↑ Hemming, N.G.; Hanson, G.N. (January 1992). "Boron isotopic composition and concentration in modern marine carbonates". Geochimica et Cosmochimica Acta. 56 (1): 537–543. Bibcode:1992GeCoA..56..537H. doi:10.1016/0016-7037(92)90151-8.
  34. ↑ Jones, R.W. (1996). Micropalaeontology in petroleum exploration. Clarendon Press. ISBN 978-0-19-854091-5.
  35. ↑ McNeil, D.H.; Issler, D.R.; Snowdon, L.R. (1996). Colour Alteration, Thermal Maturity, and Burial Diagenesis in Fossil Foraminifers. Geological Survey of Canada Bulletin. 499. Geological Survey of Canada. ISBN 978-0-660-16451-9.

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