A Microbial Biorealm page on the Foraminifera
Higher order taxa:
Haplophragmoides bradyi, Amphistegina gibbosa, Globorotalia menardii
NCBI: Taxonomy Genome
Description and Significance
Foraminifera fossils appeared during the Early Cambrian period. There are about 4,000 known species. Only 40 of these are planktonic (floating in the upper water column); the rest are benthic (dwelling at the bottom).
Foraminifera have the largest and most diverse small subunit (SSU) ribosomal RNA genes of any eukaryote. Plasmodiophorids, which have commonly been considered fungi, are related to Foraminifera. Archibald and Keeling (2004) performed genetic analysis on plasmodiophorids and found that Foraminifera are ancestors of these organisms. Other researchers, such as Pawlowski et. al. (2003) have classified species of Foraminifera through genetic analysis. Pawlowski et. al. determined that Xenophyophorea are highly specialized Foraminifera based on their study of SSU rRNA.
Cell Structure and Metabolism
Foraminifera are testate organisms, which means that they have shells (tests). The protoplasm covers the exterior of the test. The simplest shapes are tubes or spheres. The tests are divided into chambers; more chambers are added as the cell grows. There are three basic test compositions: organic, agglutinated, and secreted calcium carbonate. Organic tests are composed of protinaceous mucopolysaccharides such as allogromina. Agglutinated forms usually consist of either randomly accumulated grains or selected grains. The secreted calcium carbonate tests are further subdivided into microgranular, porcelaneous, and hyaline categories. Microgranular tests are composed of crystalline calcite; the grains are subspherical and equidimensional. Porcelaneous tests are comprised of a thick middle layer and two thin outer layers. These tests are made of high magnesium calcite. Hyaline tests add a new layer to the entire organism when a new chamber forms. This test structure is known for its pores.
Foraminifera are single-celled organisms. They can have one or many nuclei. Foraminifera also possess granuloreticulose pseudopodia. These threadlike structures often contain particles of various materials. A distinguishing structure in Foraminifera is the foramen, a hole that connects the wall (septa) between each chamber.
Foraminifera are heterotrophic organisms. Many are opportunistic feeders that prey on other autotrophic and heterotrophic protists. They also consume metazoa, dissolved free amino acids, and bacteria.
The alternation of sexual and asexual generations is common in Foraminifera species. Asexual haploid generations form a large inner chamber known as the proloculus; these are termed megalospheric. The proloculus is smaller when produced by sexual diploid generations; these are termed microspheric. Reproductive cycles tend to be short.
Foraminifera are aquatic organisms, found in both freshwater and marine environments. For example, Amphistegina gibbosa inhabit coral reefs and carbonate shelves. Species diversity is highest in tropical areas. Foraminifera are the most prevalent benthic organisms in deep-sea fossil records, but some are planktic. There are many characteristics which influence foraminiferal distribution, such as sediment type, food availability, oxygen levels, and hydrostatic pressure. However, species can tolerate a wide range of unfavorable conditions. Low concentrations of foraminifera in benthic regions may indicate an environment under stress. Foraminifera often form symbiotic relationships with algae.
Although Foraminifera can be predators, they are also prey for some organisms. Worms, crustacea, gastropods, echinoderms, and fish all prey on Foraminifera.
Archibald JM, Keeling PJ. "Actin and ubiquitin protein sequences support a cercozoan/foraminiferan ancestry for the plasmodiophorid plant pathogens." The Journal of eukaryotic microbiology. 2004 Jan-Feb;51(1):113-8.
Habura A, Rosen DR, Bowser SS. "Predicted secondary structure of the foraminiferal SSU 3' major domain reveals a molecular synapomorphy for granuloreticulosean protists." The Journal of eukaryotic microbiology. 2004 Jul-Aug;51(4):464-71.
Pawlowski J, Holzmann M, Berney C, Fahrni J, Gooday AJ, Cedhagen T, Habura A, Bowser SS. "The evolution of early Foraminifera." Proceedings of the National Academy of Sciences of the United States of America. 2003 Sep 30;100(20):11494-8. Epub 2003 Sep 22.
Pawlowski J, Holzmann M, Fahrni J, Richardson SL. "Small subunit ribosomal DNA suggests that the xenophyophorean Syringammina corbicula is a foraminiferan." The Journal of eukaryotic microbiology. 2003 Nov-Dec;50(6):483-7.
Talge HK, Hallock P. "Ultrastructural responses in field-bleached and experimentally stressed Amphistegina gibbosa (Class Foraminifera)." The Journal of eukaryotic microbiology. 2003 Sep-Oct;50(5):324-33.
Vilela CG, Batista DS, Batista-Neto JA, Crapez M, McAllister JJ. "Benthic foraminifera distribution in high polluted sediments from Niteroi Harbor (Guanabara Bay), Rio de Janeiro, Brazil." Anais da Academia Brasileira de Ciencias. 2004 Mar;76(1):161-71. Epub 2004 Mar 4.