Bioerosion

{{short description|Erosion of hard substrates by living organisms}}

File:BoredEncrustedShell.JPG borings (Entobia) and encrusters on a modern bivalve shell, North Carolina.]]

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This definition describes the chemical process of bioerosion, specifically as it applies to biorelated polymers and applications, rather than the geological concept, as covered in the article text.

Surface degradation resulting from the action of cells.

Note 1: Erosion is a general characteristic of biodegradation by cells that adhere to a surface and the molar mass of the bulk does not change, basically.

Note 2: Chemical degradation can present the characteristics of cell-mediated erosion when the rate of chemical chain scission is greater than the rate of penetration of the cleaving chemical reagent, like diffusion of water in the case
of hydrolytically degradable polymer, for instance.

Note 3: Erosion with constancy of the bulk molar mass is also observed in the case of in vitro abiotic enzymatic degradation.

Note 4: In some cases, bioerosion results from a combination of cell-mediated and chemical degradation, actually.

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Bioerosion describes the breakdown of hard ocean substrates – and less often terrestrial substrates – by living organisms. Marine bioerosion can be caused by mollusks, polychaete worms, phoronids, sponges, crustaceans, echinoids, and fish; it can occur on coastlines, on coral reefs, and on ships; its mechanisms include biotic boring, drilling, rasping, and scraping. On dry land, bioerosion is typically performed by pioneer plants or plant-like organisms such as lichen, and mostly chemical (e.g. by acidic secretions on limestone) or mechanical (e.g. by roots growing into cracks) in nature.{{citation needed|date=March 2025}}

Bioerosion of coral reefs generates the fine and white coral sand characteristic of tropical islands. The coral is converted to sand by internal bioeroders such as algae, fungi, bacteria (microborers) and sponges (Clionaidae), bivalves (including Lithophaga), sipunculans, polychaetes, acrothoracican barnacles and phoronids, generating extremely fine sediment with diameters of 10 to 100 micrometres. External bioeroders include sea urchins (such as Diadema) and chitons. These forces in concert produce a great deal of erosion. Sea urchin erosion of calcium carbonate has been reported in some reefs at annual rates exceeding 20 kg/m2.{{citation needed|date=March 2025}}

Fish also erode coral while eating algae. Parrotfish cause a great deal of bioerosion using well developed jaw muscles, tooth armature, and a pharyngeal mill, to grind ingested material into sand-sized particles. In one study, bioerosion of coral reef aragonite by an individual parrotfish was estimated to occur at a rate of 1017.7±186.3 kg/yr (0.41±0.07 m3/yr) for Chlorurus gibbus and 23.6±3.4 kg/yr (9.7*10−3±1.3*10−3 m3/yr) for Chlorurus sordidus.

Bioerosion is also well known in the fossil record on shells and hardgrounds, with traces of this activity stretching back well into the Precambrian. Macrobioerosion, which produces borings visible to the naked eye, shows two distinct evolutionary radiations. One was in the Middle Ordovician (the Ordovician Bioerosion Revolution) and the other in the Jurassic. Microbioerosion also has a long fossil record and its own radiations.

Gallery

Image:LibertyBorings.jpg|Trypanites borings in an Upper Ordovician hardground, southeastern Indiana.

Image:Petroxestes_borings_Ordovician.jpg|Petroxestes borings in an Upper Ordovician hardground, southern Ohio.

Image:CarmelHdgd.jpg|Gastrochaenolites borings in a Middle Jurassic hardground, southern Utah.

Image:FaringdonCobble.JPG|Numerous borings in a Cretaceous cobble, Faringdon, England.

Image:JurRockgd01.jpg|Cross-section of a Jurassic rockground; borings include Gastrochaenolites (some with boring bivalves in place) and Trypanites; Mendip Hills, England; scale bar = 1 cm.

Image:Teredolites.jpg|Teredolites borings in a modern wharf piling; the work of bivalves known as "shipworms".

Image:OrdHdgd03.jpg|Ordovician hardground cross-section with Trypanites borings filled with dolomite; southern Ohio.

Image:GastrochaenolitesMatmor.jpg|Gastrochaenolites boring in a recrystallized scleractinian coral, Matmor Formation (Middle Jurassic) of southern Israel.

Image:Osprioneides_kampto1.jpg|Osprioneides borings in a Silurian stromatoporoid from Saaremaa, Estonia.

Image:Gnathichnus Cenomanian 020413.JPG|Gnathichnus pentax echinoid trace fossil on an oyster from the Cenomanian of Hamakhtesh Hagadol, southern Israel.

Image:Geopetal Structure.jpg|Geopetal structure in bivalve boring in coral; bivalve shell visible; Matmor Formation (Middle Jurassic), southern Israel.

Image:Bioeroded brown bodies large.jpg|Borings in an Upper Ordovician bryozoan, Bellevue Formation, northern Kentucky; polished cross-section.

See also

  • {{annotated link|Biopitting}}
  • {{annotated link|Geomorphology}}
  • {{annotated link|Biogeomorphology}}
  • {{annotated link|Coastal erosion}}
  • Marine biogenic calcification

References

{{reflist|

{{cite journal|title=Terminology for biorelated polymers and applications (IUPAC Recommendations 2012)|journal=Pure and Applied Chemistry|year=2012|volume=84|issue=2|pages=377–410|doi=10.1351/PAC-REC-10-12-04|url=http://pac.iupac.org/publications/pac/pdf/2012/pdf/8402x0377.pdf|last1=Vert|first1=Michel|last2=Doi|first2=Yoshiharu|last3=Hellwich|first3=Karl-Heinz|last4=Hess|first4=Michael|last5=Hodge|first5=Philip|last6=Kubisa|first6=Przemyslaw|last7=Rinaudo|first7=Marguerite|last8=Schué|first8=François|s2cid=98107080|access-date=2013-07-27|archive-date=2015-03-19|archive-url=https://web.archive.org/web/20150319032817/http://pac.iupac.org/publications/pac/pdf/2012/pdf/8402x0377.pdf|url-status=dead}}

{{cite journal|last=Palmer|first=T. J.|year=1982|title=Cambrian to Cretaceous changes in hardground communities|journal=Lethaia|volume=15|issue=4|pages=309–323|doi=10.1111/j.1502-3931.1982.tb01696.x|bibcode=1982Letha..15..309P|doi-access=free}}

{{cite journal|last=Bellwood|first=D. R.|year=1995|title=Direct estimate of bioerosion by two parrotfish species, Chlorurus gibbus and C. sordidus, on the Great Barrier Reef, Australia|journal=Marine Biology|volume=121|issue=3|pages=419–429|doi=10.1007/BF00349451|bibcode=1995MarBi.121..419B |s2cid=85045930}}

{{cite book|last=Bromley|first=R. G|chapter=Borings as trace fossils and Entobia cretacea Portlock as an example|editor=Crimes, T.P. |editor2=Harper, J.C. |title=Trace Fossils|year=1970|series=Geological Journal Special Issue 3|pages=49–90}}

{{cite journal|last=Taylor|first=P. D.|author2=Wilson, M. A.|year=2003|title=Palaeoecology and evolution of marine hard substrate communities|url=http://www3.wooster.edu/geology/Taylor%26Wilson2003.pdf|journal=Earth-Science Reviews|volume=62|issue=1–2|pages=1–103|doi=10.1016/S0012-8252(02)00131-9|bibcode=2003ESRv...62....1T|url-status=dead|archive-url=https://web.archive.org/web/20090325233234/http://www.wooster.edu/geology/Taylor%26Wilson2003.pdf|archive-date=2009-03-25}}

{{cite journal|last=Wilson|first=M. A.|author2=Palmer, T. J.|year=2006|title=Patterns and processes in the Ordovician Bioerosion Revolution|url=http://www3.wooster.edu/geology/WilsonPalmer06.pdf|journal=Ichnos|volume=13|issue=3|pages=109–112|doi=10.1080/10420940600850505|bibcode=2006Ichno..13..109W |s2cid=128831144|url-status=dead|archive-url=https://web.archive.org/web/20081216220233/http://www.wooster.edu/geology/WilsonPalmer06.pdf|archive-date=2008-12-16}}

{{cite book|last=Bromley|first=R. G.|chapter=A stratigraphy of marine bioerosion|editor=D. McIlroy |title=The application of ichnology to palaeoenvironmental and stratigraphic analysis|publisher=Geological Society|location= London|year=2004|isbn=1-86239-154-8|pages=455–481|series=Geological Society of London, Special Publications 228}}

{{cite book|last=Wilson|first=M. A.|chapter=Macroborings and the evolution of bioerosion|editor=Miller III, W |title=Trace fossils: concepts, problems, prospects|publisher=Elsevier|location=Amsterdam|year=2007|isbn=978-0-444-52949-7|pages=356–367}}

{{cite journal|last=Glaub|first=I.|author2=Vogel, K.|year=2004|title=The stratigraphic record of microborings|journal=Fossils & Strata |issn=0300-9491|volume=51|pages=126–135|doi=10.18261/9781405169851-2004-08 |isbn=9781405169851}}

{{cite book|last=Glaub|first=I. |author2=Golubic, S. |author3=Gektidis, M. |author4=Radtke, G. |author5=Vogel, K.|chapter=Microborings and microbial endoliths: geological implications|editor=Miller III, W |title=Trace fossils: concepts, problems, prospects|publisher=Elsevier|location=Amsterdam|year=2007|isbn=978-0-444-52949-7|pages=368–381}}

{{cite journal|last=Wilson|first=M. A.|author2=Palmer, T. J.|year=2001|title=Domiciles, not predatory borings: a simpler explanation of the holes in Ordovician shells analyzed by Kaplan and Baumiller, 2000|journal=PALAIOS|volume=16|issue=5|pages=524–525|doi=10.1669/0883-1351(2001)016<0524:DNPBAS>2.0.CO;2|bibcode=2001Palai..16..524W|s2cid=130036115 }}

{{cite journal|last=Wilson|first=M. A.|author2=Palmer, T. J.|year=1994|title=A carbonate hardground in the Carmel Formation (Middle Jurassic, SW Utah, USA) and its associated encrusters, borers and nestlers|journal=Ichnos|volume=3|issue=2|pages=79–87|doi=10.1080/10420949409386375|bibcode=1994Ichno...3...79W}}

{{cite journal|last=Wilson|first=M. A.|year=1986|title=Coelobites and spatial refuges in a Lower Cretaceous cobble-dwelling hardground fauna|journal=Palaeontology|issn=0031-0239|volume=29|pages=691–703}}

{{cite journal|last=Vinn|first=O.|author2=Wilson, M. A.|author3=Mõtus, M.-A.|title=The Earliest Giant Osprioneides Borings from the Sandbian (Late Ordovician) of Estonia | year = 2014|journal=PLOS ONE|volume=9 | issue = 6: e99455|doi=10.1371/journal.pone.0099455|bibcode = 2014PLoSO...999455V|pages=e99455|pmid=24901511|pmc=4047083|doi-access=free}}

}}

Further reading

  • {{cite journal

| doi = 10.1080/10420940.2010.502478

| title = Occurrence of giant borings of Osprioneides kampto in the lower Silurian (Sheinwoodian) stromatoporoids of Saaremaa, Estonia

| year = 2010

| author = Vinn, O.

| author2 = Wilson, M.A.

| journal = Ichnos

| volume = 17

| issue = 3

| pages = 166–171

| bibcode = 2010Ichno..17..166V

| s2cid = 128990588

| url = https://www.researchgate.net/publication/222089796

| access-date = 2014-06-10}}

  • {{cite journal

| doi = 10.4267/2042/35594

| title = Early large borings from a hardground of Floian-Dapingian age (Early and Middle Ordovician) in northeastern Estonia (Baltica)

| year = 2010

| author = Vinn, O.

| author2 = Wilson, M.A.

| journal = Carnets de Géologie

| volume = 2010

| pages = CG2010_L04

| doi-access = free

}}

  • {{cite journal

| doi = 10.1371/journal.pone.0134279

| title = Bioerosion of Inorganic Hard Substrates in the Ordovician of Estonia (Baltica)

| year = 2015

| author = Vinn, O.

| author2 = Wilson, M.A.

| author3 = Toom, U.

| journal = PLOS ONE

| volume = 10 | issue = 7

| pages = e0134279

| pmid=26218582

| pmc=4517899| bibcode = 2015PLoSO..1034279V| doi-access = free

}}