Stercomata
Stercomata (or stercomes) are extracellular pellets of waste material produced by some groups of foraminiferans, including xenophyophoreans and komokiaceans, Gromia, and testate amoebae. The pellets are ovoid (egg-shaped), brownish in color, and on average measure from 10-20 µm in length.[1] Stercomata are composed of small mineral grains and undigested waste products held together by strands of glycosaminoglycans.[2]
The term “sterkome” was first used Schaudinn in 1899 to describe the balls of undigested food remains produced by the testate amoeba Trichosphaerium sieboldi, the foraminiferan Saccammina sphaerica, and the gromiid Gromia dujardinii.[3] Schaudinn conducted feeding experiments on live individuals of Trichosphaerium sieboldi kept in culture dishes to confirm that stercomata were accumulations of waste material produced as a byproduct of feeding.
Taxonomic distribution
Foraminifera
Stercomata are produced by members of several different subclades of Foraminifera that possess organic-walled or agglutinated tests, including: single-chambered taxa with spherical organic-walled tests (e.g., Bathyallogromia and other undescribed species),[4] single-chambered taxa with sac-like agglutinated tests (e.g., Saccammina and Leptammina),[5] single-chambered taxa with tubular agglutinated tests (e.g., Bathysiphon),[6] multi-chambered taxa with organic-walled tests (e.g., Nodellum and Resigella),[7] taxa with complex agglutinated tests composed of delicate branching tubes (Komokioidea),[8] and deep-sea taxa with large, complex tests agglutinated tests (Xenophyophorea).[1]
Xenophyophores
In xenophyophores, the stercomata are contained within an organic tubes called stercomare.
Gromiida
Gromiida is a subclade of Endomyxa, a clade that branches within the more inclusive group Rhizaria, a clade that encompasses a diverse array free-living and parasitic single-celled eukaryotes that possess branching or anastomosing pseudopodia and complex life cycles.[9] [10]
In Gromia, the only described genus of Gromiida, stercomata are spherical to ovoid in shape and range in color from brown to gray to orange.[11] [12] [13] Individual stercomes range in size from <5 µm (G. psammophila) to 15-30 µm (G. saoirsei).[13] Stercomata consist of the undigested remains of ingested food and may include mineral grains, sponge spicules and diatoms, which are held together by glycosaminoglycans.[12] [14] Unlike the stercomata in foraminiferans, the stercomata in gromiids are retained in the cytoplasm and not stored outside of the cell body; however, after the release of flagellated gametes during sexual reproduction, the stercomata remain in the interior of the test.[14]
References
- Tendal, Øle Secher (1972). "A monograph of the Xenophyophoria (Rhizopodea, Protozoa)". Galathea Report. 12: 73.
- Tendal, Øle Secher (1979). "Aspects of the biology of Komokiacea and Xenophyophoria". Sarsia. 64 (1–2): 15. doi:10.1080/00364827.1979.10411356.
- Schaudinn, Fritz (1899). "Untersuchungen über den Generationswechsel von Trichosphaerium sieboldii Schn". Abhandlungen der Königl. Akademie der Wissenschaften zu Berlin. 1898: 44. Retrieved 3 April 2022.
- Gooday, A. J.; Holzmann, M.; Guiard, J.; Cornelius, N.; Pawlowski, J. (2004). "new monothalamous foraminiferan from 1000 to 6300m water depth in the Weddell Sea: morphological and molecular characterisation". Deep Sea Research Part II: Topical Studies in Oceanography. 51 (14–16): 1611. Bibcode:2004DSRII..51.1603G. doi:10.1016/j.dsr2.2004.06.025.
- Cedhagen, T. A.; Gooday, A. J.; Pawlowski, J. (2009). "A new genus and two new species of saccamminid foraminiferans (Protista, Rhizaria) from the deep Southern Ocean". Zootaxa. 2096 (1): 15. doi:10.11646/zootaxa.2096.1.3. S2CID 15080995.
- Gooday, A. J.; Pond, D. W.; Bowser, S. S. (2002). "Ecology and nutrition of the large agglutinated foraminiferan Bathysiphon capillare in the bathyal NE Atlantic: distribution within the sediment profile and lipid biomarker composition". Marine Ecology Progress Series. 245: 69. Bibcode:2002MEPS..245...69G. doi:10.3354/meps245069.
- Gooday, A. J.; Kamenskaya, O. E.; Kitazato, H. (2008). "The enigmatic, deep‐sea, organic‐walled genera Chitinosiphon, Nodellum and Resigella (Protista, Foraminifera): A taxonomic re‐evaluation". Systematics and Biodiversity. 6 (3): 390. doi:10.1017/S1477200008002776. S2CID 86134857.
- Tendal, Ø. S.; Hessler, R. R. (1977). "An introduction to the biology and systematics of Komokiacea (Textulariina, Foraminiferida)". Galathea Report. 14: 171.
- Krabberød, A. K.; Orr, R. J. S.; Bråte, J.; Kristensen, T.; Bjørklund, K. R.; Shalchian-Tabrizi, K. (2017). "Single cell transcriptomics, mega-phylogeny and the genetic basis of morphological innovations in Rhizaria". Molecular Biology and Evolution. 34 (7): 1559. doi:10.1093/molbev/msx075. PMC 5455982. PMID 28333264.
- Cavalier-Smith, T.; Chao, E. E.; Lewis, R. (2018). "Multigene phylogeny and cell evolution of chromist infrakingdom Rhizaria: contrasting cell organisation of sister phyla Cercozoa and Retaria". Protoplasma. 255 (5): 1523. doi:10.1007/s00709-018-1241-1. PMC 6133090. PMID 29666938.
- Jepps, M. W. (1926). "Contribution to the study of Gromia oviformis Dujardin". Quarterly Journal of Microscopical Science. s2-70 (280): 701.
- Hedley, R. H. (1962). "Gromia oviformis (Rhizopodea) from New Zealand with comments on the fossil Chitinozoa". New Zealand Journal of Science. 5 (2): 122.
- Gooday, A. J.; Holzmann, M.; Majewski, W.; Pawlowski, J. (2022). "New species of Gromia (Protista, Rhizaria) from South Georgia and the Falkland Islands". Polar Biology. 45 (4): 655. doi:10.1007/s00300-022-03017-4. S2CID 246790431.
- Hedley, R. H.; Bertaud, W. S. (1962). "Electron-microscopic observations of Gromia oviformis (Sarcodina)". Journal of Protozoology. 9 (1): 81. doi:10.1111/j.1550-7408.1962.tb02585.x.