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{{Short description|Type of sedimentary rock}} {{Other uses}} {{pp-move}} {{pp-semi-indef}} {{Use dmy dates|date=October 2021}} {{Infobox rock |name = Limestone |type = Sedimentary |image = ElTorcal0408.jpg |caption = Limestone outcrop in the [[Torcal de Antequera]] nature reserve of [[Málaga]], Spain |composition = [[Calcium carbonate]]: inorganic crystalline [[calcite]] or organic calcareous material }} '''Limestone''' is a type of [[carbonate rock|carbonate]] [[sedimentary rock]] which is the main source of the material [[Lime (material)|lime]]. It is composed mostly of the [[minerals]] [[calcite]] and [[aragonite]], which are different [[Polymorphism (materials science)|crystal forms]] of [[calcium carbonate]] {{chem2|CaCO3}}. Limestone forms when these minerals [[Precipitation (chemistry)|precipitate]] out of water containing dissolved calcium. This can take place through both biological and nonbiological processes, though biological processes, such as the accumulation of corals and shells in the sea, have likely been more important for the last 540 million years.<ref>{{cite book |last1=Boggs |first1=Sam |title=Principles of sedimentology and stratigraphy |date=2006 |publisher=Pearson Prentice Hall |location=Upper Saddle River, N.J. |isbn=0-13-154728-3|edition=4th |pages=177, 181}}</ref><ref>{{Cite book|last=Leong|first=Goh Cheng|url=https://books.google.com/books?id=XhJ4RAAACAAJ&q=certificate+physical+and+human+geography|title=Certificate Physics And Human Geography; Indian Edition|date=1995-10-27|publisher=Oxford University Press|isbn=0-19-562816-0|pages=62|language=en}}</ref> Limestone often contains [[fossil]]s which provide scientists with information on ancient environments and on the [[evolution]] of life.{{sfn|Boggs|2006|p=159}} About 20% to 25% of sedimentary rock is carbonate rock, and most of this is limestone.<ref>{{cite book |last1=Blatt |first1=Harvey |last2=Tracy |first2=Robert J. |title=Petrology : igneous, sedimentary, and metamorphic. |date=1996 |publisher=W.H. Freeman |location=New York |isbn=0-7167-2438-3 |pages=295–300 |edition=2nd}}</ref>{{sfn|Boggs|2006|p=159}} The remaining carbonate rock is mostly [[Dolomite (rock)|dolomite]], a closely related rock, which contains a high percentage of the mineral [[Dolomite (mineral)|dolomite]], {{chem2|CaMg(CO3)2}}. ''Magnesian limestone'' is an obsolete and poorly-defined term used variously for dolomite, for limestone containing significant dolomite (''dolomitic limestone''), or for any other limestone containing a significant percentage of [[magnesium]].<ref>{{cite book |editor1-last=Jackson |editor1-first=Julia A. |title=Glossary of geology. |date=1997 |publisher=American Geological Institute |location=Alexandria, Virginia |isbn=0-922152-34-9 |edition=Fourth |chapter=Magnesian limestone}}</ref> Most limestone was formed in shallow marine environments, such as [[continental shelves]] or [[Carbonate platform|platforms]], though smaller amounts were formed in many other environments. Much dolomite is secondary dolomite, formed by chemical alteration of limestone.<ref>{{cite book |last1=Blatt |first1=Harvey |last2=Middleton |first2=Gerard |last3=Murray |first3=Raymond |title=Origin of sedimentary rocks |date=1980 |publisher=Prentice-Hall |location=Englewood Cliffs, N.J. |isbn=0-13-642710-3 |edition=2d |pages=446, 510–531}}</ref>{{sfn|Boggs|2006|p=182–194}} Limestone is exposed over large regions of the Earth's surface, and because limestone is slightly [[solubility|soluble]] in rainwater, these exposures often are eroded to become [[karst]] landscapes. Most [[cave]] systems are found in limestone bedrock. Limestone has numerous uses: as a chemical [[feedstock]] for the production of [[Lime (material)|lime]] used for [[cement]] (an essential component of [[concrete]]), as aggregate for the base of roads, as white pigment or filler in products such as toothpaste or paint, as a [[soil conditioner]], and as a popular decorative addition to [[rock gardens]]. Limestone formations contain about 30% of the world's [[petroleum reservoir]]s.{{sfn|Boggs|2006|p=159}} == Description == [[File:Limestone Eocene deposit at Sinj Stari grad - Dalmatia - Croatia IMG 20210820 083857.jpg|thumb|This limestone deposit in the [[karst]] of [[Dinaric Alps]] near [[Sinj]], [[Croatia]], was formed in the [[Eocene]]. ]] Limestone is composed mostly of the [[minerals]] [[calcite]] and [[aragonite]], which are different [[Polymorphism (materials science)|crystal forms]] of [[calcium carbonate]] ({{chem2|CaCO3}}). [[Dolomite (mineral)|Dolomite]], {{chem2|CaMg(CO3)2}}, is an uncommon mineral in limestone, and [[siderite]] or other [[carbonate mineral]]s are rare. However, the calcite in limestone often contains a few percent of [[magnesium]]. Calcite in limestone is divided into low-magnesium and high-magnesium calcite, with the dividing line placed at a composition of 4% magnesium. High-magnesium calcite retains the calcite mineral structure, which is distinct from dolomite. Aragonite does not usually contain significant magnesium.{{sfn|Blatt|Middleton|Murray|1980|p=448–449}} Most limestone is otherwise chemically fairly pure, with [[Detritus (geology)|clastic sediments]] (mainly fine-grained [[quartz]] and [[clay mineral]]s) making up less than 5%{{sfn|Blatt|Tracy|1996|p=295}} to 10%{{sfn|Boggs|2006|p=160}} of the composition. Organic matter typically makes up around 0.2% of a limestone and rarely exceeds 1%.{{sfn|Blatt|Middleton|Murray|1980|p=467}} Limestone often contains variable amounts of [[silica]] in the form of [[chert]] or siliceous skeletal fragments (such as [[sponge]] spicules, [[diatoms]], or [[radiolarians]]).{{sfn|Blatt|Tracy|1996|pp=301-302}} [[Fossil]]s are also common in limestone.{{sfn|Boggs|2006|p=159}} Limestone is commonly white to gray in color. Limestone that is unusually rich in organic matter can be almost black in color, while traces of [[iron]] or [[manganese]] can give limestone an off-white to yellow to red color. The density of limestone depends on its porosity, which varies from 0.1% for the densest limestone to 40% for chalk. The density correspondingly ranges from 1.5 to 2.7 g/cm<sup>3</sup>. Although relatively soft, with a [[Mohs hardness]] of 2 to 4, dense limestone can have a crushing strength of up to 180 [[MPa]].<ref>{{cite journal |last1=Oates |first1=Tony |title=Lime and Limestone |journal=Kirk-Othmer Encyclopedia of Chemical Technology |date=17 September 2010 |pages=1–53 |doi=10.1002/0471238961.1209130507212019.a01.pub3|isbn=978-0-471-23896-6 }}</ref> For comparison, [[concrete]] typically has a crushing strength of about 40 MPa.<ref>{{cite encyclopedia |chapter=Compressive strength test |title=Encyclopedia Britannica |chapter-url=https://www.britannica.com/technology/compressive-strength-test |access-date=4 February 2021}}</ref> Although limestones show little variability in mineral composition, they show great diversity in texture.{{sfn|Blatt|Tracy|1996|pp=295-296}} However, most limestone consists of sand-sized grains in a carbonate mud matrix. Because limestones are often of biological origin and are usually composed of sediment that is deposited close to where it formed, classification of limestone is usually based on its grain type and mud content.{{sfn|Blatt|Tracy|1996|p=295}} ===Grains=== [[File:Ooids, Joulter Cays, Bahamas.jpg|thumb|[[Ooid]]s from a [[beach]] on Joulter's Cay, [[The Bahamas]] ]] [[File:Ooids Carmel Formation Jurassic.jpg|thumb|Ooids in limestone of the [[Carmel Formation]] (Middle Jurassic) of southwestern Utah.]] [[File:CarmelOoids.jpg|thumb|Thin-section view of a Middle [[Jurassic]] limestone in southern [[Utah]], U.S. The round grains are [[ooid]]s; the largest is {{cvt|1.2|mm|in|2}} in diameter. This limestone is an oosparite.]] Most grains in limestone are skeletal fragments of marine organisms such as [[coral]] or [[foraminifera]].{{sfn|Blatt|Middleton|Murray|1980|p=452}} These organisms secrete structures made of aragonite or calcite, and leave these structures behind when they die. Other carbonate grains composing limestones are [[ooids]], [[peloids]], and limeclasts ([[intraclasts]] and {{ill|extraclast|lt=extraclasts|ca}}).{{sfn|Blatt|Tracy|1996|pages=295–300}} Skeletal grains have a composition reflecting the organisms that produced them and the environment in which they were produced.{{sfn|Blatt|Middleton|Murray|1980|p=449}} Low-magnesium calcite skeletal grains are typical of articulate [[brachiopod]]s, planktonic (free-floating) foraminifera, and [[coccolith]]s. High-magnesium calcite skeletal grains are typical of benthic (bottom-dwelling) foraminifera, [[echinoderm]]s, and [[coralline algae]]. Aragonite skeletal grains are typical of [[mollusc]]s, calcareous [[green algae]], [[stromatoporoid]]s, [[coral]]s, and [[tube worm]]s. The skeletal grains also reflect specific geological periods and environments. For example, coral grains are more common in high-energy environments (characterized by strong currents and turbulence) while bryozoan grains are more common in low-energy environments (characterized by quiet water).{{sfn|Boggs|2006|p=161–164}} Ooids (sometimes called ooliths) are sand-sized grains (less than 2mm in diameter) consisting of one or more layers of calcite or aragonite around a central quartz grain or carbonate mineral fragment. These likely form by direct precipitation of calcium carbonate onto the ooid. Pisoliths are similar to ooids, but they are larger than 2 mm in diameter and tend to be more irregular in shape. Limestone composed mostly of ooids is called an ''[[oolite]]'' or sometimes an ''oolitic limestone''. Ooids form in high-energy environments, such as the Bahama platform, and oolites typically show [[Cross-bedding|crossbedding]] and other features associated with deposition in strong currents.{{sfn|Blatt|Tracy|1996|pp=297-299}}{{sfn|Boggs|2006|pp=164-165}} ''Oncoliths'' resemble ooids but show a radial rather than layered internal structure, indicating that they were formed by algae in a normal marine environment.{{sfn|Blatt|Tracy|1996|pp=297-299}} Peloids are structureless grains of microcrystalline carbonate likely produced by a variety of processes.<ref>{{cite journal |last1=Adachi |first1=Natsuko |last2=Ezaki |first2=Yoichi |last3=Liu |first3=Jianbo |title=The fabrics and origins of peloids immediately after the end-Permian extinction, Guizhou Province, South China |journal=Sedimentary Geology |date=February 2004 |volume=164 |issue=1–2 |pages=161–178 |doi=10.1016/j.sedgeo.2003.10.007|bibcode=2004SedG..164..161A }}</ref> Many are thought to be fecal pellets produced by marine organisms. Others may be produced by [[endolithic]] (boring) algae{{sfn|Blatt|Tracy|1996|p=298}} or other microorganisms<ref>{{cite journal |last1=Chafetz |first1=Henry S. |title=Marine Peloids: A Product of Bacterially Induced Precipitation of Calcite |journal=SEPM Journal of Sedimentary Research |date=1986 |volume= 56 |issue=6 |pages=812–817 |doi=10.1306/212F8A58-2B24-11D7-8648000102C1865D}}</ref> or through breakdown of mollusc shells.<ref>{{cite journal |last1=Samankassou |first1=Elias |last2=Tresch |first2=Jonas |last3=Strasser |first3=André |title=Origin of peloids in Early Cretaceous deposits, Dorset, South England |journal=Facies |date=26 November 2005 |volume=51 |issue=1–4 |pages=264–274 |doi=10.1007/s10347-005-0002-8|bibcode=2005Faci...51..264S |s2cid=128851366 |url=http://doc.rero.ch/record/322424/files/10347_2005_Article_2.pdf }}</ref> They are difficult to see in a limestone sample except in thin section and are less common in ancient limestones, possibly because compaction of carbonate sediments disrupts them.{{sfn|Blatt|Tracy|1996|p=298}} Limeclasts are fragments of existing limestone or partially [[lithification|lithified]] carbonate sediments. Intraclasts are limeclasts that originate close to where they are deposited in limestone, while extraclasts come from outside the depositional area. Intraclasts include ''grapestone'', which is clusters of peloids cemented together by organic material or mineral cement. Extraclasts are uncommon, are usually accompanied by other clastic sediments, and indicate deposition in a tectonically active area or as part of a [[turbidity current]].{{sfn|Blatt|Tracy|1996|p=299–300, 304}} ===Mud=== The grains of most limestones are embedded in a matrix of carbonate mud. This is typically the largest fraction of an ancient carbonate rock.{{sfn|Blatt|Tracy|1996|p=298}} Mud consisting of individual crystals less than {{convert|5|µm|mil|abbr=in}} in length is described as ''micrite''.{{sfn|Blatt|Middleton|Murray|1980|p=460}} In fresh carbonate mud, micrite is mostly small aragonite needles, which may precipitate directly from seawater,{{sfn|Blatt|Tracy|1996|p=300}} be secreted by algae,{{sfn|Boggs|2006|p=166}} or be produced by abrasion of carbonate grains in a high-energy environment.<ref name="trower-etal-2019"/> This is converted to calcite within a few million years of deposition. Further recrystallization of micrite produces ''microspar'', with grains from {{convert|5|to|15|µm|mil|abbr=in}} in diameter.{{sfn|Blatt|Tracy|1996|p=300}} Limestone often contains larger crystals of calcite, ranging in size from {{convert|0.02|to|0.1|mm|mil|abbr=in}}, that are described as ''sparry calcite'' or ''sparite''. Sparite is distinguished from micrite by a grain size of over {{convert|20|µm|mil|abbr=in}} and because sparite stands out under a hand lens or in thin section as white or transparent crystals. Sparite is distinguished from carbonate grains by its lack of internal structure and its characteristic crystal shapes.{{sfn|Boggs|2006|pp=166-167}} Geologists are careful to distinguish between sparite deposited as cement and sparite formed by recrystallization of micrite or carbonate grains. Sparite cement was likely deposited in pore space between grains, suggesting a high-energy depositional environment that removed carbonate mud. Recrystallized sparite is not diagnostic of depositional environment.{{sfn|Boggs|2006|pp=166-167}} ===Other characteristics=== [[File:Seven Sisters 3.jpg|thumb|The [[Beachy Head]] cliffs are composed of chalk.]] Limestone outcrops are recognized in the [[Field work|field]] by their softness (calcite and aragonite both have a Mohs hardness of less than 4, well below common silicate minerals) and because limestone bubbles vigorously when a drop of dilute [[hydrochloric acid]] is dropped on it. Dolomite is also soft but reacts only feebly with dilute hydrochloric acid, and it usually weathers to a characteristic dull yellow-brown color due to the presence of ferrous iron. This is released and oxidized as the dolomite weathers.{{sfn|Blatt|Tracy|1996|p=295}} Impurities (such as [[clay]], sand, organic remains, [[iron oxide]], and other materials) will cause limestones to exhibit different colors, especially with [[Weathering|weathered]] surfaces. The makeup of a carbonate rock outcrop can be estimated in the field by etching the surface with dilute hydrochloric acid. This etches away the calcite and aragonite, leaving behind any silica or dolomite grains. The latter can be identified by their [[rhombohedral]] shape.{{sfn|Blatt|Tracy|1996|p=295}} Crystals of calcite, [[quartz]], [[Dolomite (mineral)|dolomite]] or [[barite]] may line small cavities (''[[vugs]]'') in the rock. Vugs are a form of secondary porosity, formed in existing limestone by a change in environment that increases the solubility of calcite.{{sfn|Blatt|Tracy|1996|pp=315-317}} Dense, massive limestone is sometimes described as "marble". For example, the famous [[Portoro marble|Portoro "marble"]] of Italy is actually a dense black limestone.<ref>{{cite journal |last1=Fratini |first1=Fabio |last2=Pecchioni |first2=Elena |last3=Cantisani |first3=Emma |last4=Antonelli |first4=Fabrizio |last5=Giamello |first5=Marco |last6=Lezzerini |first6=Marco |last7=Canova |first7=Roberta |title=Portoro, the black and gold Italian "marble" |journal=Rendiconti Lincei |date=December 2015 |volume=26 |issue=4 |pages=415–423 |doi=10.1007/s12210-015-0420-7|s2cid=129625906 }}</ref> True [[marble]] is produced by recrystallization of limestone during regional [[metamorphism]] that accompanies the mountain building process ([[orogeny]]). It is distinguished from dense limestone by its coarse crystalline texture and the formation of distinctive minerals from the silica and clay present in the original limestone.{{sfn|Blatt|Tracy|1996|pp=474}} ===Classification=== {{See also|List of types of limestone}} [[File:Pamukkale 12.jpg|thumb|[[Travertine]] limestone terraces of [[Pamukkale]], [[Turkey]].]] [[File:Luray Caverns, Dream Lake - mirror-lake of caverns (2015-05-09 14.03.28 by Stan Mouser).jpg|thumb|[[Cave formations|Cave limestone formations]] in the [[Luray Caverns]] of the northern [[Shenandoah Valley]]]]Two major classification schemes, the Folk and Dunham, are used for identifying the types of [[carbonate rocks]] collectively known as limestone. ====Folk classification==== {{main|Folk's carbonate classification}} [[Robert L. Folk]] developed a classification system that places primary emphasis on the detailed composition of grains and interstitial material in [[carbonate rocks]].<ref>{{cite web| url = http://sepmstrata.org/page.aspx?pageid=89| title = Carbonate Classification: SEPM STRATA}}</ref> Based on composition, there are three main components: allochems (grains), matrix (mostly micrite), and cement (sparite). The Folk system uses two-part names; the first refers to the grains and the second to the cement. For example, a limestone consisting mainly of ooids, with a crystalline matrix, would be termed an oosparite. It is helpful to have a [[petrographic microscope]] when using the Folk scheme, because it is easier to determine the components present in each sample.<ref name="Folk">{{cite book |last=Folk |first=R. L. |year=1974 |title=Petrology of Sedimentary Rocks |publisher=Hemphill Publishing |location=Austin, Texas |isbn=0-914696-14-9}}</ref> ====Dunham classification==== {{main|Dunham classification}} Robert J. Dunham published his system for limestone in 1962. It focuses on the depositional fabric of carbonate rocks. Dunham divides the rocks into four main groups based on relative proportions of coarser clastic particles, based on criteria such as whether the grains were originally in mutual contact, and therefore self-supporting, or whether the rock is characterized by the presence of frame builders and algal mats. Unlike the Folk scheme, Dunham deals with the original porosity of the rock. The Dunham scheme is more useful for hand samples because it is based on texture, not the grains in the sample.<ref name="Dunham">{{cite book |last=Dunham |first=R. J. |year=1962 |chapter=Classification of carbonate rocks according to depositional textures |editor-last=Ham |editor-first=W. E. |title=Classification of Carbonate Rocks |series=American Association of Petroleum Geologists Memoirs |volume=1 |pages=108–121 }}</ref> A revised classification was proposed by Wright (1992). It adds some diagenetic patterns to the classification scheme.<ref name="Wright1992">{{cite journal |last1=Wright |first1=V.P.|year=1992 |title=A revised Classification of Limestones |journal=Sedimentary Geology |volume=76 |issue=3–4 |pages=177–185 |doi=10.1016/0037-0738(92)90082-3 |bibcode=1992SedG...76..177W}}</ref> ====Other descriptive terms==== [[File:Chalk ("Upper Chalk" Formation, Upper Cretaceous; White Cliffs of Dover, England, southern Britain).jpg|thumb|Chalk from the White Cliffs of Dover ([[Chalk Group]]), England]] ''[[Travertine]]'' is a term applied to calcium carbonate deposits formed in freshwater environments, particularly [[waterfall]]s, cascades and [[hot springs]]. Such deposits are typically massive, dense, and banded. When the deposits are highly porous, so that they have a spongelike texture, they are typically described as ''[[tufa]]''. Secondary calcite deposited by [[Supersaturation|supersaturated]] [[meteoric water]]s ([[groundwater]]) in caves is also sometimes described as travertine. This produces [[speleothem]]s, such as [[stalagmite]]s and [[stalactite]]s.{{sfn|Blatt|Middleton|Murray|1980|p=479–480}} ''[[Coquina]]'' is a poorly consolidated limestone composed of abraded pieces of [[coral]], [[Exoskeleton|shells]], or other fossil debris. When better consolidated, it is described as ''coquinite''.{{sfn|Boggs|2006|p=172}} ''[[Chalk]]'' is a soft, earthy, fine-textured limestone composed of the tests of planktonic microorganisms such as foraminifera, while ''[[marl]]'' is an earthy mixture of carbonates and silicate sediments.{{sfn|Boggs|2006|p=172}} {{clear}} == Formation == Limestone forms when calcite or aragonite [[Precipitation (chemistry)|precipitate]] out of water containing dissolved calcium, which can take place through both biological and nonbiological processes.{{sfn|Boggs|2006|p=177}} The solubility of calcium carbonate ({{chem2|CaCO3}}) is controlled largely by the amount of dissolved [[carbon dioxide]] ({{chem2|CO2}}) in the water. This is summarized in the reaction: :{{chem2|CaCO3 + H2O + CO2 -> Ca(2+) + 2 HCO3−}} Increases in temperature or decreases in pressure tend to reduce the amount of dissolved {{chem2|CO2}} and precipitate {{chem2|CaCO3}}. Reduction in salinity also reduces the solubility of {{chem2|CaCO3}}, by several orders of magnitude for fresh water versus seawater.{{sfn|Boggs|2006|pages=174–176}} Near-surface water of the earth's oceans are oversaturated with {{chem2|CaCO3}} by a factor of more than six.<ref>{{cite book |last1=Morse |first1=John W. |last2=Mackenzie |first2=F. T. |title=Geochemistry of sedimentary carbonates |date=1990 |publisher=Elsevier |location=Amsterdam |isbn=0-08-086962-9|page=217}}</ref> The failure of {{chem2|CaCO3}} to rapidly precipitate out of these waters is likely due to interference by dissolved magnesium [[ion]]s with [[nucleation]] of calcite crystals, the necessary first step in precipitation. Precipitation of aragonite may be suppressed by the presence of naturally occurring organic phosphates in the water. Although [[ooids]] likely form through purely inorganic processes, the bulk of {{chem2|CaCO3}} precipitation in the oceans is the result of biological activity.{{sfn|Boggs|2006|pp=176-182}} Much of this takes place on [[carbonate platform]]s. [[File:Lake Ontario Whiting NASA Satellite Image.jpg|thumb|An aerial view of a whiting event precipitation cloud in Lake Ontario.]] The origin of carbonate mud,<ref name="trower-etal-2019">{{cite journal |last1=Trower |first1=Elizabeth J. |last2=Lamb |first2=Michael P. |last3=Fischer |first3=Woodward W. |title=The Origin of Carbonate Mud |journal=Geophysical Research Letters |date=16 March 2019 |volume=46 |issue=5 |pages=2696–2703 |doi=10.1029/2018GL081620|bibcode=2019GeoRL..46.2696T |s2cid=134970335 }}</ref> and the processes by which it is converted to micrite,<ref>{{cite journal |last1=Jerry Lucia |first1=F. |title=Observations on the origin of micrite crystals |journal=Marine and Petroleum Geology |date=September 2017 |volume=86 |pages=823–833 |doi=10.1016/j.marpetgeo.2017.06.039|bibcode=2017MarPG..86..823J }}</ref> continue to be a subject of research. Modern carbonate mud is composed mostly of aragonite needles around {{convert|5|µm|mil|abbr=in}} in length. Needles of this shape and composition are produced by calcareous algae such as ''[[Penicillus (alga)|Penicillus]]'', making this a plausible source of mud.{{sfn|Blatt|Middleton|Murray|1980|pp=460-464}} Another possibility is direct precipitation from the water. A phenomenon known as ''whitings'' occurs in shallow waters, in which white streaks containing dispersed micrite appear on the surface of the water. It is uncertain whether this is freshly precipitated aragonite or simply material stirred up from the bottom, but there is some evidence that whitings are caused by biological precipitation of aragonite as part of a [[Algal bloom|bloom]] of [[cyanobacteria]] or [[microalgae]].{{sfn|Boggs|2006|p=180}} However, [[stable isotope ratio]]s in modern carbonate mud appear to be inconsistent with either of these mechanisms, and abrasion of carbonate grains in high-energy environments has been put forward as a third possibility.<ref name="trower-etal-2019"/> Formation of limestone has likely been dominated by biological processes throughout the [[Phanerozoic]], the last 540 million years of the Earth's history. Limestone may have been deposited by microorganisms in the [[Precambrian]], prior to 540 million years ago, but inorganic processes were probably more important and likely took place in an ocean more highly oversaturated in calcium carbonate than the modern ocean.{{sfn|Boggs|2006|pp=177, 181}} ===Diagenesis=== [[Diagenesis]] is the process in which sediments are compacted and [[lithification|turned into solid rock]]. During diagenesis of carbonate sediments, significant chemical and textural changes take place. For example, aragonite is converted to low-magnesium calcite. Diagenesis is the likely origin of ''pisoliths'', concentrically layered particles ranging from {{convert|1|to|10|mm|in|abbr=in}} in diameter found in some limestones. Pisoliths superficially resemble ooids but have no nucleus of foreign matter, fit together tightly, and show other signs that they formed after the original deposition of the sediments.{{sfn|Blatt|Middleton|Murray|1980|pp=497–501}} [[File:Çört yumrusu, Chert.2.jpg|thumb|Chert nodule within soft limestone at [[Akçakoca]], Turkey]] [[File:Stylolites mcr1.jpg|thumb|right|[[Stylolite]]s in limestone]] Silicification occurs early in diagenesis, at low pH and temperature, and contributes to fossil preservation.<ref name="Götz-2017">{{Cite journal |last1=Götz |first1=Annette E. |last2=Montenari |first2=Michael |last3=Costin |first3=Gelu |date=2017 |title=Silicification and organic matter preservation in the Anisian Muschelkalk: Implications for the basin dynamics of the central European Muschelkalk Sea |url=https://akjournals.com/view/journals/24/60/1/article-p35.xml |journal=Central European Geology |volume=60 |issue=1 |pages=35–52 |doi=10.1556/24.60.2017.002 |bibcode=2017CEJGl..60...35G |issn=1788-2281 |doi-access=free}}</ref> Silicification takes place through the reaction:<ref name="Götz-2017" /> :{{chem2|CaCO3 + H2O + CO2 + H4SiO4 -> SiO2 + Ca(2+) + 2 HCO3- + 2 H2O }} Fossils are often preserved in exquisite detail as chert.<ref name="Götz-2017" />{{sfn|Blatt|Middleton|Murray|1980|p=497–503}} Cementing takes place rapidly in carbonate sediments, typically within less than a million years of deposition. Some cementing occurs while the sediments are still under water, forming [[hardground]]s. Cementing accelerates after the retreat of the sea from the depositional environment, as rainwater infiltrates the sediment beds, often within just a few thousand years. As rainwater mixes with groundwater, aragonite and high-magnesium calcite are converted to low-calcium calcite. Cementing of thick carbonate deposits by rainwater may commence even before the retreat of the sea, as rainwater can infiltrate over {{convert|100|km|mi|abbr=in|sigfig=1}} into sediments beneath the continental shelf.{{sfn|Blatt|Tracy|1996|p=312}} As carbonate sediments are increasingly deeply buried under younger sediments, chemical and mechanical compaction of the sediments increases. Chemical compaction takes place by ''[[pressure solution]]'' of the sediments. This process dissolves minerals from points of contact between grains and redeposits it in pore space, reducing the porosity of the limestone from an initial high value of 40% to 80% to less than 10%.{{sfn|Blatt|Middleton|Murray|1980|pp=507-509}} Pressure solution produces distinctive [[stylolite]]s, irregular surfaces within the limestone at which silica-rich sediments accumulate. These may reflect dissolution and loss of a considerable fraction of the limestone bed. At depths greater than {{convert|1|km|mi|abbr=in}}, burial cementation completes the lithification process. Burial cementation does not produce stylolites.{{sfn|Blatt|Tracy|1996|p=312–316}} When overlying beds are eroded, bringing limestone closer to the surface, the final stage of diagenesis takes place. This produces ''secondary porosity'' as some of the cement is dissolved by rainwater infiltrating the beds. This may include the formation of [[vug]]s, which are crystal-lined cavities within the limestone.{{sfn|Blatt|Tracy|1996|p=312–316}} Diagenesis may include conversion of limestone to dolomite by magnesium-rich fluids. There is considerable evidence of replacement of limestone by dolomite, including sharp replacement boundaries that cut across bedding.{{sfn|Boggs|2006|pp=186-187}} The process of [[dolomitization]] remains an area of active research,<ref name="machel-2004">{{cite journal |last1=Machel |first1=Hans G. |title=Concepts and models of dolomitization: a critical reappraisal |journal=Geological Society, London, Special Publications |date=2004 |volume=235 |issue=1 |pages=7–63 |doi=10.1144/GSL.SP.2004.235.01.02|bibcode=2004GSLSP.235....7M |s2cid=131159219 }}</ref> but possible mechanisms include exposure to concentrated brines in hot environments (''evaporative reflux'') or exposure to diluted seawater in delta or estuary environments (''Dorag dolomitization'').{{sfn|Blatt|Middleton|Murray|1980|pp=512-528}} However, Dorag dolomitization has fallen into disfavor as a mechanism for dolomitization,<ref>{{cite journal |last1=Luczaj |first1=John A. |title=Evidence against the Dorag (mixing-zone) model for dolomitization along the Wisconsin arch ― A case for hydrothermal diagenesis |journal=AAPG Bulletin |date=November 2006 |volume=90 |issue=11 |pages=1719–1738 |doi=10.1306/01130605077|bibcode=2006BAAPG..90.1719L }}</ref> with one 2004 review paper describing it bluntly as "a myth".<ref name="machel-2004"/> Ordinary seawater is capable of converting calcite to dolomite, if the seawater is regularly flushed through the rock, as by the ebb and flow of tides (tidal pumping).{{sfn|Boggs|2006|pp=186-187}} Once dolomitization begins, it proceeds rapidly, so that there is very little carbonate rock containing mixed calcite and dolomite. Carbonate rock tends to be either almost all calcite/aragonite or almost all dolomite.{{sfn|Blatt|Middleton|Murray|1980|pp=512-528}} == Occurrence == About 20% to 25% of sedimentary rock is carbonate rock,{{sfn|Boggs|2006|p=159}} and most of this is limestone.{{sfn|Blatt|Tracy|1996|pp=295–300}}{{sfn|Boggs|2006|p=159}} Limestone is found in sedimentary sequences as old as 2.7 billion years.{{sfn|Blatt|Middleton|Murray|1980|p=445}} However, the compositions of carbonate rocks show an uneven distribution in time in the geologic record. About 95% of modern carbonates are composed of high-magnesium calcite and aragonite.{{sfn|Blatt|Middleton|Murray|1980|p=448}} The aragonite needles in carbonate mud are converted to low-magnesium calcite within a few million years, as this is the most stable form of calcium carbonate.{{sfn|Blatt|Tracy|1996|p=300}} Ancient carbonate formations of the [[Precambrian]] and [[Paleozoic]] contain abundant dolomite, but limestone dominates the carbonate beds of the [[Mesozoic]] and [[Cenozoic]]. Modern dolomite is quite rare. There is evidence that, while the modern ocean favors precipitation of aragonite, the oceans of the Paleozoic and middle to late Cenozoic favored precipitation of calcite. This may indicate a lower Mg/Ca ratio in the ocean water of those times.{{sfn|Boggs|2006|p=159-161}} This magnesium depletion may be a consequence of more rapid [[sea floor spreading]], which removes magnesium from ocean water. The modern ocean and the ocean of the Mesozoic have been described as "aragonite seas".{{sfn|Boggs|2006|p=176-177}} Most limestone was formed in shallow marine environments, such as [[continental shelves]] or [[Carbonate platform|platforms]]. Such environments form only about 5% of the ocean basins, but limestone is rarely preserved in continental slope and deep sea environments. The best environments for deposition are warm waters, which have both a high organic productivity and increased saturation of calcium carbonate due to lower concentrations of dissolved carbon dioxide. Modern limestone deposits are almost always in areas with very little silica-rich sedimentation, reflected in the relative purity of most limestones. Reef organisms are destroyed by muddy, brackish river water, and carbonate grains are ground down by much harder silicate grains.{{sfn|Blatt|Middleton|Murray|1980|p=446, 733}} Unlike clastic sedimentary rock, limestone is produced almost entirely from sediments originating at or near the place of deposition.{{sfn|Blatt|Middleton|Murray|1980|p=468-470}} [[File:El Cap GUMO.jpg|thumb|[[El Capitan (Texas)|El Capitan]], an ancient limestone reef in Texas]] Limestone formations tend to show abrupt changes in thickness. Large moundlike features in a limestone formation are interpreted as ancient [[reef]]s, which when they appear in the geologic record are called ''bioherms''. Many are rich in fossils, but most lack any connected organic framework like that seen in modern reefs. The fossil remains are present as separate fragments embedded in ample mud matrix. Much of the sedimentation shows indications of occurring in the intertidal or supratidal zones, suggesting sediments rapidly fill available [[Accommodation (geology)|accommodation space]] in the shelf or platform.{{sfn|Blatt|Middleton|Murray|1980|p=446-447}} Deposition is also favored on the seaward margin of shelves and platforms, where there is upwelling deep ocean water rich in nutrients that increase organic productivity. Reefs are common here, but when lacking, ooid shoals are found instead. Finer sediments are deposited close to shore.{{sfn|Blatt|Tracy|1996|p=306-307}} The lack of deep sea limestones is due in part to rapid [[subduction]] of oceanic crust, but is more a result of dissolution of calcium carbonate at depth. The solubility of calcium carbonate increases with pressure and even more with higher concentrations of carbon dioxide, which is produced by decaying organic matter settling into the deep ocean that is not removed by [[photosynthesis]] in the dark depths. As a result, there is a fairly sharp transition from water saturated with calcium carbonate to water unsaturated with calcium carbonate, the ''[[lysocline]]'', which occurs at the ''[[calcite compensation depth]]'' of {{convert|4000|to|7000|m|ft|abbr=in}}. Below this depth, foraminifera tests and other skeletal particles rapidly dissolve, and the sediments of the ocean floor abruptly transition from carbonate ooze rich in foraminifera and coccolith remains (''[[Globigerina]]'' ooze) to silicic mud lacking carbonates.{{sfn|Blatt|Middleton|Murray|1980|p=474-479}} [[File:Mønsted kalkgruber exposure fused 2014-07-18.jpg|thumb|[[Mønsted]] is the largest limestone [[Mining|mine]] in the world.]] In rare cases, [[turbidite]]s or other silica-rich sediments bury and preserve benthic (deep ocean) carbonate deposits. Ancient benthic limestones are microcrystalline and are identified by their tectonic setting. Fossils typically are foraminifera and coccoliths. No pre-Jurassic benthic limestones are known, probably because carbonate-shelled plankton had not yet evolved.{{sfn|Blatt|Tracy|1996|p=308-309}} Limestones also form in freshwater environments.<ref>{{Cite journal|last1=Roeser|first1=Patricia|last2=Franz|first2=Sven O.|last3=Litt|first3=Thomas|date=1 December 2016|title=Aragonite and calcite preservation in sediments from Lake Iznik related to bottom lake oxygenation and water column depth|journal=Sedimentology|language=en|volume=63|issue=7|pages=2253–2277|doi=10.1111/sed.12306|s2cid=133211098 |issn=1365-3091}}</ref> These limestones are not unlike marine limestone, but have a lower diversity of organisms and a greater fraction of silica and clay minerals characteristic of [[marl]]s. The [[Green River Formation]] is an example of a prominent freshwater sedimentary formation containing numerous limestone beds.{{sfn|Blatt|Middleton|Murray|1980|p=480-482}} Freshwater limestone is typically micritic. Fossils of [[charophyte]] (stonewort), a form of freshwater green algae, are characteristic of these environments, where the charophytes produce and trap carbonates.{{sfn|Blatt|Tracy|1996|p=309-310}} Limestones may also form in [[evaporite]] [[Sedimentary depositional environment|depositional environments]].<ref>{{cite journal |last1=Trewin |first1=N. H. |last2=Davidson |first2=R. G. |year=1999 |title=Lake-level changes, sedimentation and faunas in a Middle Devonian basin-margin fish bed |journal=[[Journal of the Geological Society]] |volume=156 |issue=3 |pages=535–548 |doi=10.1144/gsjgs.156.3.0535 |bibcode=1999JGSoc.156..535T |s2cid=131241083 }}</ref><ref>{{cite web|url=http://www.glossary.oilfield.slb.com/Display.cfm?Term=evaporite|url-status=dead|website=Oilfield Glossary|title=Term 'evaporite'|archive-url=https://web.archive.org/web/20120131020924/http://www.glossary.oilfield.slb.com/Display.cfm?Term=evaporite |archive-date=31 January 2012 |access-date=25 November 2011}}</ref> Calcite is one of the first minerals to precipitate in marine evaporites.{{sfn|Boggs|2006|p=662}} ===Limestone and living organisms=== [[File:Lembongan-penida-snorkeling.jpg|thumb|Coral reef at [[Nusa Lembongan]], Bali, Indonesia]] Most limestone is formed by the activities of living organisms near reefs, but the organisms responsible for reef formation have changed over geologic time. For example, ''[[stromatolites]]'' are mound-shaped structures in ancient limestones, interpreted as colonies of [[cyanobacteria]] that accumulated carbonate sediments, but stromatolites are rare in younger limestones.{{sfn|Blatt|Middleton|Murray|1980|pp=446, 471-474}} Organisms precipitate limestone both directly as part of their skeletons, and indirectly by removing carbon dioxide from the water by photosynthesis and thereby decreasing the solubility of calcium carbonate.{{sfn|Blatt|Tracy|1996|p=309-310}} Limestone shows the same range of [[sedimentary structures]] found in other sedimentary rocks. However, finer structures, such as [[Lamination (geology)|lamination]], are often destroyed by the burrowing activities of organisms ([[bioturbation]]). Fine lamination is characteristic of limestone formed in [[playa lake]]s, which lack the burrowing organisms.{{sfn|Blatt|Middleton|Murray|1980|pp=446-471}} Limestones also show distinctive features such as ''geopetal structures'', which form when curved shells settle to the bottom with the concave face downwards. This traps a void space that can later be filled by sparite. Geologists use geopetal structures to determine which direction was up at the time of deposition, which is not always obvious with highly deformed limestone formations.{{sfn|Blatt|Tracy|1996|p=304}} The [[cyanobacterium]] ''Hyella balani'' can bore through limestone; as can the [[green alga]] ''Eugamantia sacculata'' and the [[fungus]] ''Ostracolaba implexa''.<ref>{{cite book|url=https://books.google.com/books?id=GerdDmwMTLkC&pg=PA178|title=Geomicrobiology|edition=5th|first1=Henry Lutz |last1=Ehrlich|first2=Dianne K. |last2=Newman|year=2009|pages=181–182|publisher=CRC Press |isbn=978-0-8493-7907-9|url-status=live|archive-url=https://web.archive.org/web/20160510231918/https://books.google.com/books?id=GerdDmwMTLkC&pg=PA178|archive-date=10 May 2016}}</ref> ====Micritic mud mounds==== Micricitic mud mounds are subcircular domes of micritic calcite that lacks internal structure. Modern examples are up to several hundred meters thick and a kilometer across, and have steep slopes (with slope angles of around 50 degrees). They may be composed of peloids swept together by currents and stabilized by ''[[Thalassia (plant)|Thalassia]]'' grass or [[mangroves]]. Bryozoa may also contribute to mound formation by helping to trap sediments.{{sfn|Blatt|Tracy|1996|p=307}} Mud mounds are found throughout the geologic record, and prior to the [[early Ordovician]], they were the dominant reef type in both deep and shallow water. These mud mounds likely are microbial in origin. Following the appearance of frame-building reef organisms, mud mounds were restricted mainly to deeper water.<ref>{{cite journal |last1=Pratt |first1=Brian R. |title=The origin, biota, and evolution of deep-water mud-mounds |journal=Spec. Publs Int. Ass. Sediment. |date=1995 |volume=23 |pages=49–123 |isbn=1-4443-0412-7 |url=https://books.google.com/books?id=4QCWd-BiJ04C&q=micritic+mud+mounds&pg=PA49 |access-date=4 February 2021}}</ref> ====Organic reefs==== Organic reefs form at low latitudes in shallow water, not more than a few meters deep. They are complex, diverse structures found throughout the fossil record. The frame-building organisms responsible for organic reef formation are characteristic of different geologic time periods: [[Archaeocyathid]]s appeared in the [[early Cambrian]]; these gave way to sponges by the [[late Cambrian]]; later successions included stromatoporoids, corals, algae, bryozoa, and [[rudist]]s (a form of bivalve mollusc).{{sfn|Blatt|Tracy|1996|pp=307-308}}<ref>{{cite journal |last1=Riding |first1=Robert |title=Structure and composition of organic reefs and carbonate mud mounds: concepts and categories |journal=Earth-Science Reviews |date=July 2002 |volume=58 |issue=1–2 |pages=163–231 |doi=10.1016/S0012-8252(01)00089-7|bibcode=2002ESRv...58..163R }}</ref><ref>{{cite book |last1=Wood |first1=Rachel |title=Reef evolution |date=1999 |publisher=Oxford University Press |location=Oxford |isbn=0-19-857784-2|url=https://books.google.com/books?id=H_ah6Hzib4AC&q=reef+organisms+by+geologic+period&pg=PA3 |access-date=5 February 2021}}</ref> The extent of organic reefs has varied over geologic time, and they were likely most extensive in the middle Devonian, when they covered an area estimated at {{convert|5000000|km2|sqmi|abbr=on}}. This is roughly ten times the extent of modern reefs. The Devonian reefs were constructed largely by stromatoporoids and [[Tabulata|tabulate corals]], which were devastated by the [[late Devonian extinction]].<ref>{{cite book |last1=McGhee |first1=George R. |title=When the invasion of land failed : the legacy of the Devonian extinctions |date=2013 |publisher=Columbia University Press |location=New York |isbn=978-0-231-16057-5 |page=101}}</ref> Organic reefs typically have a complex internal structure. Whole body fossils are usually abundant, but ooids and interclasts are rare within the reef. The core of a reef is typically massive and unbedded, and is surrounded by a [[Scree|talus]] that is greater in volume than the core. The talus contains abundant intraclasts and is usually either ''floatstone'', with 10% or more of grains over 2mm in size embedded in abundant matrix, or ''rudstone'', which is mostly large grains with sparse matrix. The talus grades to planktonic fine-grained carbonate mud, then noncarbonate mud away from the reef.{{sfn|Blatt|Tracy|1996|pp=307-308}} == Limestone landscape == {{Main|Karst topography}} [[File:Maczuga Herkulesa (background Castle Pieskowa Skała).jpg|thumb|left|[[Maczuga Herkulesa|The Cudgel of Hercules]], a tall limestone rock in Poland ([[Pieskowa Skała|Pieskowa Skała Castle]] in the background)]] [[File:Cenote in valladolid mexico (21362599476).jpg|thumb|The [[Samulá]] [[cenote]] in [[Valladolid Municipality, Yucatán|Valladolid]], [[Yucatán]], [[Mexico]]]][[File:La Zaplaz, Piatra Craiului.jpg|thumb|La Zaplaz formations in the [[Piatra Craiului Mountains]], [[Romania]].]]Limestone is partially soluble, especially in acid, and therefore forms many erosional landforms. These include [[limestone pavement]]s, [[pot hole]]s, [[cenote]]s, caves and gorges. Such erosion landscapes are known as [[karsts]]. Limestone is less [[resistance (geology)|resistant]] to erosion than most [[igneous]] rocks, but more resistant than most other [[sedimentary rock]]s. It is therefore usually associated with hills and [[downland]], and occurs in regions with other sedimentary rocks, typically clays.<ref name="thornbury-1969">{{cite book |last1=Thornbury |first1=William D. |title=Principles of geomorphology |date=1969 |publisher=Wiley |location=New York |isbn=0-471-86197-9 |pages=303–344 |edition=2d}}</ref><ref>{{cite web |title=Karst Landscapes of Illinois: Dissolving Bedrock and Collapsing Soil |url=https://isgs.illinois.edu/outreach/geology-resources/karst-landscapes-illinois-dissolving-bedrock-and-collapsing-soil |website=Prairie Research Institute |publisher=Illinois State Geological Survey |access-date=26 December 2020 |archive-date=2 December 2020 |archive-url=https://web.archive.org/web/20201202003934/https://isgs.illinois.edu/outreach/geology-resources/karst-landscapes-illinois-dissolving-bedrock-and-collapsing-soil |url-status=dead }}</ref> Karst regions overlying limestone bedrock tend to have fewer visible above-ground sources (ponds and streams), as surface water easily drains downward through [[Joint (geology)|joints]] in the limestone. While draining, water and organic acid from the soil slowly (over thousands or millions of years) enlarges these cracks, dissolving the calcium carbonate and carrying it away in [[Solution (chemistry)|solution]]. Most [[cave]] systems are through limestone bedrock. Cooling groundwater or mixing of different groundwaters will also create conditions suitable for cave formation.<ref name="thornbury-1969" /> Coastal limestones are often eroded by organisms which bore into the rock by various means. This process is known as [[bioerosion]]. It is most common in the tropics, and it is known throughout the [[fossil record]].<ref>{{cite journal|last1=Taylor|first1=P. D.|last2=Wilson|first2=M. A.|date=2003|title=Palaeoecology and evolution of marine hard substrate communities|journal=Earth-Science Reviews|volume=62|issue=1–2|pages=1–103|bibcode=2003ESRv...62....1T|doi=10.1016/S0012-8252(02)00131-9|url=http://www.wooster.edu/geology/Taylor%26Wilson2003.pdf|archive-url=https://web.archive.org/web/20090325233234/http://www.wooster.edu/geology/Taylor%26Wilson2003.pdf|url-status=dead|archive-date=2009-03-25}}</ref> Bands of limestone emerge from the Earth's surface in often spectacular rocky outcrops and islands. Examples include the [[Rock of Gibraltar]],<ref name="Quaternary Science Reviews 23 (2004) 2017–2029">{{cite journal |last1=Rodrı́guez-Vidal |first1=J. |last2=Cáceres |first2=L.M. |last3=Finlayson |first3=J.C. |last4=Gracia |first4=F.J. |last5=Martı́nez-Aguirre |first5=A. |title=Neotectonics and shoreline history of the Rock of Gibraltar, southern Iberia |journal=Quaternary Science Reviews |date=October 2004 |volume=23 |issue=18–19 |pages=2017–2029 |doi=10.1016/j.quascirev.2004.02.008 |url=https://www.researchgate.net/publication/257823064|publisher=Elsevier (2004)|bibcode=2004QSRv...23.2017R |hdl=11441/137125 |access-date=23 June 2016|hdl-access=free }}</ref> the [[The Burren|Burren]] in County Clare, Ireland;<ref>{{cite web |last1=McNamara |first1=M. |last2= Hennessy |first2=R. |year=2010 |title=The geology of the Burren region, Co. Clare, Ireland |website=Project NEEDN, The Burren Connect Project |location=Ennistymon |publisher=Clare County Council |url=https://www.burrengeopark.ie/wp-content/uploads/2014/08/NEED-THE_GEOLOGY_OF_THE_BURREN_REGIONBurren-Techni.pdf |access-date=3 February 2021}}</ref> [[Malham Cove]] in [[North Yorkshire]] and the [[Isle of Wight]],<ref>{{cite web| url=http://www.iwight.com/council/documents/policies_and_plans/udp/2002_pdfs/minerals.pdf| title=Isle of Wight, Minerals| access-date=8 October 2006| url-status=dead| archive-url=https://web.archive.org/web/20061102184845/http://www.iwight.com/council/documents/policies_and_plans/udp/2002_pdfs/minerals.pdf| archive-date=2 November 2006}}</ref> England; the [[Great Orme]] in Wales;<ref>{{cite journal |last1=Juerges |first1=A. |last2=Hollis |first2=C. E. |last3=Marshall |first3=J. |last4=Crowley |first4=S. |title=The control of basin evolution on patterns of sedimentation and diagenesis: an example from the Mississippian Great Orme, North Wales |journal=Journal of the Geological Society |date=May 2016 |volume=173 |issue=3 |pages=438–456 |doi=10.1144/jgs2014-149|bibcode=2016JGSoc.173..438J |doi-access=free }}</ref> on [[Fårö]] near the Swedish island of [[Gotland]],<ref>{{cite journal |last1=Cruslock |first1=Eva M. |last2=Naylor |first2=Larissa A. |last3=Foote |first3=Yolanda L. |last4=Swantesson |first4=Jan O.H. |title=Geomorphologic equifinality: A comparison between shore platforms in Höga Kusten and Fårö, Sweden and the Vale of Glamorgan, South Wales, UK |journal=Geomorphology |date=January 2010 |volume=114 |issue=1–2 |pages=78–88 |doi=10.1016/j.geomorph.2009.02.019|bibcode=2010Geomo.114...78C }}</ref> the [[Niagara Escarpment]] in Canada/United States;<ref>{{cite journal |last1=Luczaj |first1=John A. |title=Geology of the Niagara Escarpment in Wisconsin |journal=Geoscience Wisconsin |date=2013 |volume=22 |issue=1 |pages=1–34 |url=https://www.researchgate.net/publication/325576131 |access-date=5 February 2021}}</ref> [[Notch Peak]] in Utah;<ref>{{cite journal |jstor=1302317|title=Conodont Fauna of the Notch Peak Limestone (Cambro-Ordovician), House Range, Utah|last1=Miller|first1=James F.|journal=Journal of Paleontology|year=1969|volume=43|issue=2|pages=413–439}}</ref> the [[Ha Long Bay]] National Park in Vietnam;<ref name=Thanh>{{cite journal|journal=Advances in Natural Sciences|volume=2|issue=3|issn=0866-708X|url=https://www.researchgate.net/publication/258604343|title=The outstanding value of the geology of Ha Long Bay|last1=Tran Duc Thanh|last2=Waltham Tony|date=1 September 2001}}</ref> and the hills around the [[Lijiang River]] and [[Guilin]] city in China.<ref name="Tony">{{cite book|last1=Waltham|first1=Tony|editor1-last=Migon|editor1-first=Piotr|title=Guangxi Karst: The Fenglin and Fengcong Karst of Guilin and Yangshuo, in Geomorphological Landscapes of the World|date=2010|publisher=Springer|isbn=978-90-481-3054-2|pages=293–302}}</ref> The [[Florida Keys]], islands off the south coast of [[Florida]], are composed mainly of [[oolite|oolitic]] limestone (the Lower Keys) and the carbonate skeletons of [[coral]] reefs (the Upper Keys), which thrived in the area during interglacial periods when sea level was higher than at present.<ref>{{Cite journal|last=Mitchell-Tapping|first=Hugh J.|date=Spring 1980|title=Depositional History of the Oolite of the Miami Limestone Formation|journal=Florida Scientist|volume=43|issue=2|pages=116–125|jstor=24319647}}</ref> Unique habitats are found on [[alvar]]s, extremely level expanses of limestone with thin soil mantles. The largest such expanse in Europe is the [[Stora Alvaret]] on the island of [[Öland]], Sweden.<ref>Thorsten Jansson, ''Stora Alvaret'', Lenanders Tryckeri, [[Kalmar]], 1999</ref> Another area with large quantities of limestone is the island of Gotland, Sweden.<ref name=Laufeld1974>{{cite book |last=Laufeld |first=S. |year=1974 |title=Silurian Chitinozoa from Gotland |publisher=Universitetsforlaget |series=Fossils and Strata |issue=5 }}</ref> Huge quarries in northwestern Europe, such as those of Mount Saint Peter (Belgium/Netherlands), extend for more than a hundred kilometers.<ref>{{cite journal |last1=Pereira |first1=Dolores |last2=Tourneur |first2=Francis |last3=Bernáldez |first3=Lorenzo |last4=Blázquez |first4=Ana García |title=Petit Granit: A Belgian limestone used in heritage, construction and sculpture |journal=Episodes |date=2014 |volume=38 |issue=2 |page=30 |bibcode=2014EGUGA..16...30P |url=http://media.globalheritagestone.com/2016/12/Petit-Granit-Episodes.pdf |access-date=5 February 2021}}</ref> == Uses == {{See also|ashlar}} [[File:Malta - Qrendi - Hagar Qim and Mnajdra Archaeological Park - Hagar Qim 08 ies.jpg|thumb|The [[Megalithic Temples of Malta]] such as [[Ħaġar Qim]] are built entirely of limestone. They are among the oldest freestanding structures in existence.<ref name=cassar>{{cite book |last= Cassar |first= Joann |year=2010 |contribution= The use of limestone in historic context |editor-last= Smith |editor-first= Bernard J. |title= Limestone in the Built Environment: Present-day Challenges for the Preservation of the Past |publisher= Geographical Society of London |pages= 13–23 |isbn=978-1-86239-294-6 |url=https://books.google.com/books?id=wXCoMb3CU4YC&pg=PA17 |access-date= 20 December 2024}}</ref>]] [[File:Gizeh Cheops BW 1.jpg|thumb|The [[Great Pyramid of Giza]], one of the [[Seven Wonders of the Ancient World]], had an outside cover made entirely from limestone.]] Limestone is a raw material that is used globally in a variety of different ways including construction, agriculture and as industrial materials.<ref name="Oates-2008" /> Limestone is very common in architecture, especially in Europe and North America. Many landmarks across the world, including the [[Great Pyramid of Giza|Great Pyramid]] and its associated [[Giza pyramid complex|complex]] in [[Giza, Egypt]], were made of limestone. So many buildings in [[Kingston, Ontario]], Canada were, and continue to be, constructed from it that it is nicknamed the 'Limestone City'.<ref>{{cite web |url= http://www.citylifeontario.com/kingston/ |title= Welcome to the Limestone City |access-date=13 February 2008 |url-status= live |archive-url= https://web.archive.org/web/20080220171909/http://www.citylifeontario.com/kingston/ |archive-date= 20 February 2008 }}</ref> Limestone, metamorphosed by heat and pressure produces marble, which has been used for many statues, buildings and stone tabletops.<ref name="Corathers-2019" /> On the island of [[Malta]], a variety of limestone called [[Globigerina Limestone Formation|Globigerina limestone]] was, for a long time, the only building material available, and is still very frequently used on all types of buildings and sculptures.<ref>{{cite journal |last1=Cassar |first1=Joann |title=The use of limestone in a historic context – the experience of Malta |journal=Geological Society, London, Special Publications |date=2010 |volume=331 |issue=1 |pages=13–25 |doi=10.1144/SP331.2|bibcode=2010GSLSP.331...13C |s2cid=129082854 }}</ref> Limestone can be processed into many various forms such as brick, cement, powdered/crushed, or as a filler.<ref name="Oates-2008">{{Cite book |last=Oates |first=J. A. H. |url=https://books.google.com/books?id=MVoEMNI5Vb0C |title=Lime and Limestone: Chemistry and Technology, Production and Uses |date=2008-07-11 |publisher=John Wiley & Sons |isbn=978-3-527-61201-7 |pages=64 |language=en |chapter=7.2 Market Overview}}</ref> Limestone is readily available and relatively easy to cut into blocks or more elaborate carving.<ref name="cassar" /> Ancient American sculptors valued limestone because it was easy to work and good for fine detail. Going back to the Late Preclassic period (by 200–100 BCE), the [[Maya civilization]] (Ancient Mexico) created refined sculpture using limestone because of these excellent carving properties. The Maya would decorate the ceilings of their sacred buildings (known as [[Ancient Maya art|lintels]]) and cover the walls with carved limestone panels. Carved on these sculptures were political and social stories, and this helped communicate messages of the king to his people.<ref>{{cite book|first1=Linda |last1=Schele |first2=Mary Ellen |last2=Miller |title=The Blood of Kings: Dynasty and Ritual in Maya Art |publisher=Kimbell Art Museum |page=41}}</ref> Limestone is long-lasting and stands up well to exposure, which explains why many limestone ruins survive. However, it is very heavy ([[density]] 2.6<ref name="Sharma1997">{{citation|author1=P. V. Sharma|title=Environmental and Engineering Geophysics|year=1997|publisher=Cambridge University Press|isbn= 1-139-17116-X|page=17|doi=10.1017/CBO9781139171168}}</ref>), making it impractical for tall buildings, and relatively expensive as a building material. Limestone was most popular in the late 19th and early 20th centuries. Railway stations, banks and other structures from that era were made of limestone in some areas. It is used as a [[façade]] on some skyscrapers, but only in thin plates for covering, rather than solid blocks. In the United States, Indiana, most notably the [[Bloomington, Indiana|Bloomington]] area, has long been a source of high-quality quarried limestone, called [[Indiana limestone]]. Many famous buildings in London are built from [[Portland limestone]]. Houses built in [[Odesa]] in [[Ukraine]] in the 19th century were mostly constructed from limestone and the extensive remains of the mines now form the [[Odesa Catacombs]].<ref name="Odesa">{{cite web |url=https://leodessa.com/odessa-catacombs/ |title=Odessa catacombs |publisher=Odessa travel guide |access-date=13 June 2020}}</ref> Limestone was also a very popular building block in the Middle Ages in the areas where it occurred, since it is hard, durable, and commonly occurs in easily accessible surface exposures. Many medieval churches and castles in Europe are made of limestone. [[Beer stone]] was a popular kind of limestone for medieval buildings in southern England.<ref name="ashurst">{{cite book|last1=Ashurst|first1=John|last2=Dimes|first2=Francis G.|title=Conservation of building and decorative stone|url=https://books.google.com/books?id=xPFx6bEPspgC&pg=PA117|year=1998|publisher=Butterworth-Heinemann|isbn=0-7506-3898-2|page=117}}</ref> <gallery> File:Limestone Mines at Cedar Creek.jpg|Limestone quarry at [[Cedar Creek (North Fork Shenandoah River)|Cedar Creek, Virginia]], US File:Pargas Quarry-24.jpg|[[Nordkalk]]'s limestone quarry in [[Pargas]], [[Finland]] File:Gozo, limestone quarry - cutting the stone.JPG|Cutting limestone blocks at a quarry in [[Gozo]], [[Malta]] File:Kalkstein (nahe).JPG|Limestone as building material File:Bermuda Number 178 limestone used as building material for walls.jpg|Limestone is used worldwide as building material. </gallery> Limestone is the raw material for production of lime, primarily known for treating soils, purifying water and [[smelting]] copper. Lime is an important ingredient used in chemical industries.<ref name="Bliss-2012-1">Bliss, J. D., Hayes, T. S., & Orris, G. J. (2012, August). Limestone—A Crucial and Versatile Industrial Mineral Commodity. Retrieved February 23, 2021, from https://pubs.usgs.gov/fs/2008/3089/fs2008-3089.pdf</ref> Limestone and (to a lesser extent) marble are reactive to acid solutions, making [[acid rain]] a significant problem to the preservation of artifacts made from this stone. Many limestone statues and building surfaces have suffered severe damage due to acid rain.<ref>{{cite journal|title=ICP on effects on materials |doi=10.1007/BF01186242 |volume=85 |issue=4 |journal=Water, Air, & Soil Pollution |pages=2701–2706|bibcode=1995WASP...85.2701R |last1=Reisener |first1=A. |last2=Stäckle |first2=B. |last3=Snethlage |first3=R. |year=1995 |s2cid=94721996 }}</ref><ref>{{cite web |url=http://www.iiasa.ac.at/Admin/PUB/Documents/WP-89-104.pdf |title=Approaches in modeling the impact of air pollution-induced material degradation |access-date=November 18, 2010 |archive-url=https://web.archive.org/web/20110716175635/http://www.iiasa.ac.at/Admin/PUB/Documents/WP-89-104.pdf |archive-date=July 16, 2011 |url-status=dead }}</ref> Likewise limestone gravel has been used to protect lakes vulnerable to acid rain, acting as a [[pH buffer]]ing agent.<ref>{{cite journal |last1=Clayton |first1=Janet L. |last2=Dannaway |first2=Eric S. |last3=Menendez |first3=Raymond |last4=Rauch |first4=Henry W. |last5=Renton |first5=John J. |last6=Sherlock |first6=Sean M. |last7=Zurbuch |first7=Peter E. |title=Application of Limestone to Restore Fish Communities in Acidified Streams |journal=North American Journal of Fisheries Management |date=1998 |volume=18 |issue=2 |pages=347–360 |doi=10.1577/1548-8675(1998)018<0347:AOLTRF>2.0.CO;2|bibcode=1998NAJFM..18..347C }}</ref> Acid-based cleaning chemicals can also etch limestone, which should only be cleaned with a neutral or mild [[alkali]]-based cleaner.<ref>{{cite web |last1=Hatch |first1=Jonathan |title=How to clean limestone |url=https://howtocleanthings.com/how-to-clean-limestone/ |website=How to Clean Things |publisher=Saint Paul Media, Inc. |access-date=5 February 2021 |date=18 April 2018}}</ref> [[File:Litography press with map of Moosburg 01.jpg|thumb|A limestone plate with a negative map of [[Moosburg]] in Bavaria is prepared for a [[lithography]] print.]] [[File:LIMEX limestone plastic, 2022 Japan 2.jpg|thumb|Plastic bag "made mainly from limestone"{{clarify|what does this actually mean?|date=April 2024}}]] Other uses include: * It is the raw material for the manufacture of [[quicklime]] (calcium oxide), [[slaked lime]] (calcium hydroxide), [[cement]] and [[mortar (masonry)|mortar]].{{sfn|Blatt|Middleton|Murray|1980|p=445}} * Pulverized limestone is used as a soil conditioner to neutralize acidic soils ([[agricultural lime]]).<ref name="Oates2008">{{cite book|first=J. A. H.|last=Oates|title=Lime and Limestone: Chemistry and Technology, Production and Uses|url=https://books.google.com/books?id=MVoEMNI5Vb0C&pg=PA111|date=11 July 2008|publisher=[[John Wiley & Sons]]|isbn=978-3-527-61201-7|pages=111–3}}</ref> * Is crushed for use as [[construction aggregate|aggregate]]—the solid base for many roads as well as in [[asphalt concrete]].{{sfn|Blatt|Middleton|Murray|1980|p=445}} * As a [[reagent]] in [[flue-gas desulfurization]], where it reacts with [[sulfur dioxide]] for air pollution control.<ref>{{cite journal |last1=Gutiérrez Ortiz |first1=F. J. |last2=Vidal |first2=F. |last3=Ollero |first3=P. |last4=Salvador |first4=L. |last5=Cortés |first5=V. |last6=Giménez |first6=A. |title=Pilot-Plant Technical Assessment of Wet Flue Gas Desulfurization Using Limestone |journal=Industrial & Engineering Chemistry Research |date=February 2006 |volume=45 |issue=4 |pages=1466–1477 |doi=10.1021/ie051316o}}</ref> * In [[glass making]], particularly in the manufacture of [[soda–lime glass]].<ref>{{Cite book|url=https://books.google.com/books?id=zNicdkuulE4C&q=Glass+making,+in+some+circumstances,+uses+limestone.&pg=PA1387|title=Industrial Minerals & Rocks: Commodities, Markets, and Uses|last=Kogel|first=Jessica Elzea|date=2006|publisher=SME|isbn=0-87335-233-5|language=en|url-status=live|archive-url=https://web.archive.org/web/20171216222141/https://books.google.com/books?id=zNicdkuulE4C&pg=PA1387&dq=Glass+making,+in+some+circumstances,+uses+limestone.&hl=en&sa=X&ved=0ahUKEwi65Iu0yI_YAhVT22MKHWTfAWgQ6AEIKTAA#v=onepage&q=Glass%20making,%20in%20some%20circumstances,%20uses%20limestone.&f=false|archive-date=16 December 2017}}</ref> * As an additive toothpaste, paper, plastics, paint, tiles, and other materials as both white pigment and a cheap filler.<ref>{{cite book |last1=Huwald |first1=Eberhard |chapter=Calcium carbonate - pigment and filler |title=Calcium Carbonate | editor-first = F. W. | editor-last = Tegethoff | publisher = Birkhäuser | location = Basel |date=2001 |pages=160–170 |doi=10.1007/978-3-0348-8245-3_7|isbn=3-0348-9490-2 }}</ref> * As [[rock dust]], to suppress methane explosions in underground coal mines.<ref>{{cite journal |last1=Man |first1=C.K. |last2=Teacoach |first2=K.A. |year=2009 |title=How does limestone rock dust prevent coal dust explosions in coal mines? |journal=Mining Engineering |page=61 |url=https://www.cdc.gov/NIOSH/Mining/UserFiles/works/pdfs/hdlrdp.pdf |access-date=30 November 2020}}</ref> * Purified, it is added to bread and cereals as a source of calcium.<ref>{{cite web |title=Why Fortified Flour? |url=https://www.wessexmill.co.uk/acatalog/Fortified-Flour.html |website=Wessex Mill |access-date=5 February 2021}}</ref> * As a calcium supplement in livestock feed, such as for poultry (when ground up).<ref>{{cite news|url= http://poultryone.com/articles/calcium.html|title= A Guide to Giving Your Layer Hens Enough Calcium|work= Poultry One|url-status= live|archive-url= https://web.archive.org/web/20090403082817/http://poultryone.com/articles/calcium.html|archive-date= 3 April 2009}}</ref> * For remineralizing and increasing the alkalinity of purified water to prevent pipe corrosion and to restore essential nutrient levels.<ref>{{cite web|url=https://www.who.int/water_sanitation_health/dwq/nutconsensus/en/|title= Nutrient minerals in drinking-water and the potential health consequences of consumption of demineralized and remineralized and altered mineral content drinking-water: Consensus of the meeting|work= World Health Organization report|url-status= dead|archive-url= https://web.archive.org/web/20071224165953/http://www.who.int/water_sanitation_health/dwq/nutconsensus/en/|archive-date= 24 December 2007}}</ref> * In [[blast furnace]]s, limestone binds with silica and other impurities to remove them from the iron.<ref>{{cite book |last1=Tylecote |first1=R. F. |title=A history of metallurgy |date=1992 |publisher=Institute of Materials |location=London |isbn=0-901462-88-8 |edition=2nd}}</ref> *It can aid in the removal of toxic components created from coal burning plants and layers of polluted molten metals.<ref name="Bliss-2012-1"/> Many limestone [[Geological formation|formation]]s are porous and permeable, which makes them important [[petroleum reservoir]]s.<ref>{{cite journal |last1=Archie |first1=G.E. |title=Classification of Carbonate Reservoir Rocks and Petrophysical Considerations |journal=AAPG Bulletin |date=1952 |volume=36 |doi=10.1306/3D9343F7-16B1-11D7-8645000102C1865D}}</ref> About 20% of North American hydrocarbon reserves are found in carbonate rock. Carbonate reservoirs are very common in the petroleum-rich Middle East,{{sfn|Blatt|Middleton|Murray|1980|p=445}} and carbonate reservoirs hold about a third of all petroleum reserves worldwide.{{sfn|Boggs|2006|p=p=159}} Limestone formations are also common sources of metal ores, because their porosity and permeability, together with their chemical activity, promotes ore deposition in the limestone. The [[lead]]-[[zinc]] deposits of [[Missouri]] and the [[Northwest Territories]] are examples of ore deposits hosted in limestone.{{sfn|Blatt|Middleton|Murray|1980|p=445}} === Scarcity === Limestone is a major industrial raw material that is in constant demand. This raw material has been essential in the [[iron]] and [[steel]] industry since the nineteenth century.<ref name="Haumann-2020">{{cite journal | title=Critical and scarce: the remarkable career of limestone 1850–1914 | last=Haumann | first=S. | journal=European Review of History: Revue européenne d'histoire | year=2020 | volume=27 | issue=3 | pages=273–293 | doi=10.1080/13507486.2020.1737651| s2cid=221052279 }}</ref> Companies have never had a shortage of limestone; however, it has become a concern as the demand continues to increase<ref name="SparenbergHeymann">{{cite journal | title=Introduction: resource challenges and constructions of scarcity in the nineteenth and twentieth centuries | last1=Sparenberg | first1=O. | last2=Heymann | first2=M. | journal=European Review of History: Revue européenne d'histoire | year=2020 | volume=27 | issue=3 | pages=243–252 | doi=10.1080/13507486.2020.1737653| s2cid=221055042 | doi-access=free }}</ref> and it remains in high demand today.<ref name="ResearchAndMarkets">{{cite web | url=https://www.businesswire.com/news/home/20200609005311/en/Global-Limestone-Market-Analysis-and-Forecasts-2020-2027---Steady-Growth-Projected-over-the-Next-Few-Years---ResearchAndMarkets.com | title=Global Limestone Market Analysis and Forecasts 2020-2027 - Steady Growth Projected over the Next Few Years - ResearchAndMarkets.com | publisher=businesswire.com | work=Limestone - Global Market Trajectory & Analytics | date=9 June 2020 | access-date=24 March 2021 | author=ResearchAndMarkets.com}}</ref> The major potential threats to supply in the nineteenth century were regional availability and accessibility.<ref name="Haumann-2020" /> The two main accessibility issues were transportation and property rights. Other problems were high capital costs on plants and facilities due to environmental regulations and the requirement of zoning and mining permits.<ref name="Corathers-2019">{{cite book | url=https://books.google.com/books?id=arqJE6h4uJ4C&pg=SA43-PA1 | chapter=Lime | title=Metals and minerals: US Geological Survey Minerals Yearbook 2014, Volume 1 | publisher=[[USGS]] | last=Corathers | first=L.A. | date=15 February 2019 | page=43.1 | publication-date=2018 | publication-place=Washington, DC |isbn=978-1-4113-4253-8}}</ref> These two dominant factors led to the adaptation and selection of other materials that were created and formed to design alternatives for limestone that suited economic demands.<ref name="Haumann-2020" /> Limestone was classified as a critical raw material, and with the potential risk of shortages, it drove industries to find new alternative materials and technological systems. This allowed limestone to no longer be classified as critical as replacement substances increased in production; [[Minette (ore)|minette ore]] is a common substitute, for example.<ref name="Haumann-2020" /> === Occupational safety and health === {{NFPA 704 | H= 1 | F= 0 | R= 0 | S= |caption=Limestone |ref=<ref name="MSDS"/>}} Powdered limestone as a food additive is [[generally recognized as safe]]<ref>{{cite web |title=CFR - Code of Federal Regulations Title 21 |url=https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=184.1409 |website=US Food & Drug Administration |publisher=US Department of Health & Human Services |access-date=5 February 2021}}</ref> and limestone is not regarded as a hazardous material. However, limestone dust can be a mild respiratory and skin irritant, and dust that gets into the eyes can cause [[corneal abrasion]]s. Because limestone contains small amounts of silica, inhalation of limestone dust could potentially lead to [[silicosis]] or [[cancer]].<ref name="MSDS">{{cite web |last1=Lhoist North America |title=Material Safety Data Sheet: Limestone |url=https://www.7springsfarm.com/content/MSDS_Limestone.pdf |access-date=5 February 2021}}</ref> ====United States==== The [[Occupational Safety and Health Administration]] (OSHA) has set the legal limit ([[permissible exposure limit]]) for limestone exposure in the workplace as {{cvt|15|mg/m3}} total exposure and {{cvt|5|mg/m3}} respiratory exposure over an 8-hour workday. The [[National Institute for Occupational Safety and Health]] (NIOSH) has set a [[recommended exposure limit]] (REL) of {{cvt|10|mg/m3}} total exposure and {{cvt|5|mg/m3}} respiratory exposure over an 8-hour workday.<ref>{{Cite web|website= NIOSH Pocket Guide to Chemical Hazards |title= Limestone|url = https://www.cdc.gov/niosh/npg/npgd0369.html|publisher= CDC|access-date =19 November 2015|url-status = live|archive-url = https://web.archive.org/web/20151120065513/http://www.cdc.gov/niosh/npg/npgd0369.html|archive-date = 20 November 2015}}</ref> === Graffiti === Removing [[graffiti]] from weathered limestone is difficult because it is a porous and permeable material. The surface is fragile, therefore usual abrasion methods run the risk of severe surface loss. Since it is an acid-sensitive stone, some cleaning agents cannot be used due to adverse effects.<ref>{{cite web |url=https://www.nps.gov/tps/how-to-preserve/briefs/38-remove-graffiti.htm |title=Removing Graffiti from Historic Masonry |first=Martin E. |last=Weaver |date=October 1995 |publisher=National Park Service |access-date=5 February 2019}}</ref> ==Gallery== <gallery> File:OrdOutcropTN.JPG|A [[stratigraphic section]] of [[Ordovician]] limestone exposed in central [[Tennessee]], U.S. The less-resistant and thinner beds are composed of [[shale]]. The vertical lines are drill holes for explosives used during road construction. File:Limestone etched section KopeFm new.jpg|Photo and etched section of a sample of [[fossiliferous limestone]] from the [[Kope Formation]] (Upper Ordovician) near [[Cincinnati]], [[Ohio]], U.S. File:BrassfieldEncrinite042112.jpg|[[biosparite]] limestone of the [[Brassfield Formation]] (Lower [[Silurian]]) near [[Fairborn]], Ohio, U.S., showing grains mainly composed of [[crinoid]] fragments File:大连国家地质公园12-龟背石.jpg|A [[concretionary]] [[nodule (geology)|nodular]] (septarian) limestone at Jinshitan Coastal National Geopark, [[Dalian]], China File:太湖賞石-Rock in the form of a fantastic mountain MET DT208239.jpg|Limestone from [[Lake Tai]], used in [[gongshi]], a Chinese stone art File:Folded Rock Provo Canyon.JPG|Folded limestone layers on [[Cascade Mountain (Utah)|Cascade Mountain]] in [[Provo Canyon]], [[Utah]] File:Calcined fossils.jpg|Fossils in limestone from the northern [[Black Sea]] region </gallery> == See also == * {{annotated link|Coral sand}} * [[Charmant Som]] * {{annotated link|In Praise of Limestone|''In Praise of Limestone''}} * {{annotated link|Kurkar}} * {{annotated link|Limepit}} * {{annotated link|Sandstone}} * {{annotated link|Liming (soil)}} == References == {{reflist|30em}} == Further reading == {{Commons category|Limestone}} {{refbegin|30em}} * {{cite book|first=Robert S.|last=Boynton|title=Chemistry and Technology of Lime and Limestone|url=https://archive.org/details/rulesdistrictco00distgoog|publisher=Wiley|date=1980|isbn=0-471-02771-5}} {{refend}} {{Rock type}} {{Authority control}} [[Category:Limestone| ]] [[Category:Industrial minerals]]
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