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Limestone - Wikipedia
Limestone - Wikipedia
Limestone - Wikipedia
Limestone
Limestone is a common type of carbonate sedimentary rock. It
is composed mostly of the minerals calcite and aragonite, which Limestone
Sedimentary rock
are different crystal forms of calcium carbonate (CaCO3).
Limestone forms when these minerals precipitate out of water
containing dissolved calcium. This can take place through both
biological and nonbiological processes, though biological
processes have likely been more important for the last 540
million years.[1] Limestone often contains fossils, and these
provide scientists with information on ancient environments and
on the evolution of life.[2]
Contents
Description
Grains
Mud
Other characteristics
Classification
Folk classification
Dunham classification
Other descriptive terms
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Formation
Diagenesis
Occurrence
Limestone and living organisms
Micritic mud mounds
Organic reefs
Limestone landscape
Uses
Scarcity
Occupational safety and health
United States
Graffiti
Gallery
See also
References
Further reading
Description
Limestone is composed mostly of the minerals calcite and aragonite, which are different crystal forms
Limestone often contains variable amounts of silica in the form of chert or siliceous skeletal
fragments (such as sponge spicules, diatoms, or radiolarians).[11] Fossils are also common in
limestone.[2]
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/cm3. Although
relatively soft, with a Mohs hardness of 2 to 4, dense limestone can have a crushing strength of up to
180 MPa.[12] For comparison, concrete typically has a crushing strength of about 40 MPa.[13]
Although limestones show little variability in mineral composition, they show great diversity in
texture.[14] 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.[8]
Grains
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Limeclasts are fragments of existing limestone or partially 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.[25]
Mud
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The grains of most limestones are embedded in a matrix of carbonate mud. This is typically the
largest fraction of an ancient carbonate rock.[22] Mud consisting of individual crystals less than 5
microns in length is described as micrite.[26] In fresh carbonate mud, micrite is mostly small
aragonite needles, which may precipitate directly from seawater,[27] be secreted by algae,[28] or be
produced by abrasion of carbonate grains in a high-energy environment.[29] This is converted to
calcite within a few million years of deposition. Further recrystallization of micrite produces
microspar, with grains from 5 to 15 microns in diameter.[27]
Limestone often contains larger crystals of calcite, ranging in size from 0.02 to 0.1 mm, that are
described as sparry calcite or sparite. Sparite is distinguished from micrite by a grain size of over 20
microns 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. [30]
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.[30]
Other characteristics
Limestone outcrops are recognized in the 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.[8]
Impurities (such as clay, sand, organic remains, iron oxide, and other materials) will cause limestones
to exhibit different colors, especially with 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.[8]
Crystals of calcite, quartz, 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.[31]
Dense, massive limestone is sometimes described as "marble". For example, the famous Portoro
"marble" of Italy is actually a dense black limestone.[32] 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.[33]
Classification
Two major classification schemes, the Folk and Dunham, are used for identifying the types of
carbonate rocks collectively known as limestone.
Folk classification
Robert L. Folk developed a classification system that places primary emphasis on the detailed
composition of grains and interstitial material in carbonate rocks.[34] Based on composition, there
are three main components: allochems (grains), matrix (mostly micrite), and cement (sparite). The
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Dunham classification
Travertine limestone terraces of Pamukkale,
Robert J. Dunham published his system for limestone in
Turkey.
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.[36]
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.[39]
Formation
Limestone forms when calcite or aragonite precipitate out of water containing dissolved calcium,
which can take place through both biological and nonbiological processes.[40] The solubility of
calcium carbonate (CaCO
3) is controlled largely by the amount of dissolved carbon dioxide (CO
2) in
the water. This is summarized in the reaction:
−
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Increases in temperature or decreases in pressure tend to reduce the amount of dissolved CO2 and
precipitate CaCO3. Reduction in salinity also reduces the solubility of CaCO3, by several orders of
magnitude for fresh water versus seawater.
[41]
Near-surface water of the earth's oceans are oversaturated with CaCO3 by a factor of more than
six.[42] The failure of CaCO3 to rapidly precipitate out of these waters is likely due to interference by
dissolved magnesium ions 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
CaCO3 precipitation in the oceans is the result of biological activity.[43] Much of this takes place on
carbonate platforms.
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.[47]
Diagenesis
Diagenesis is the process in which sediments are compacted and 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 1 to 10 millimeters (0.039 to 0.394 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.[48]
Silicification occurs early in diagenesis, at low pH and temperature, and contributes to fossil
preservation. Silicification takes place through the reaction:
−
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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 vugs, which are crystal-lined cavities within
the limestone.[52]
Occurrence
About 20% to 25% of sedimentary rock is carbonate rock,[2] and most of this is limestone.[16][2]
Limestone is found in sedimentary sequences as old as 2.7 billion years.[57] 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.[58] 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.[27] Ancient carbonate formations of the Precambrian
and Paleozoic contain abundant dolomite, but limestone dominates the carbonate beds of the
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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.[59] 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".[60]
Most limestone was formed in shallow marine environments, such as continental shelves or
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.[61] Unlike clastic sedimentary rock, limestone is
produced almost entirely from sediments originating at or near the place of deposition.[62]
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
4,000 to 7,000 meters (13,000 to 23,000 ft). 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 formanifera and coccolith remains (Globigerina ooze) to silicic mud lacking
carbonates.[65]
In rare cases, turbidites 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 limesones
are known, probably because carbonate-shelled plankton had not yet evolved.[66]
Limestones also form in freshwater environments.[67] 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 marls. The Green River Formation is an example of a prominent freshwater
sedimentary formation containing numerous limestone beds.[68] 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.[69]
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The cyanobacterium Hyella balani can bore through limestone; as can the green alga Eugamantia
sacculata and the fungus Ostracolaba implexa.[76]
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 Thallasia grass or mangroves. Bryozoa may also contribute to mound formation by
helping to trap sediments.[77]
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.[78]
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:
Archaeocyathids appeared in the early Cambrian; these gave way to sponges by the late Cambrian;
later successions included stromatoporoids, corals, algae, bryozoa, and rudists (a form of bivalve
mollusc).[79][80][81] The extent of organic reefs has varied over geologic time, and they were likely
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most extensive in the middle Devonian, when they covered an area estimated at 5,000,000 square
kilometers (1,900,000 sq mi). This is roughly ten times the extent of modern reefs. The Devonian
reefs were constructed largely by stromatoporoids and tabulate corals, which were devastated by the
late Devonian extinction.[82]
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 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.[79]
Limestone landscape
Limestone is partially soluble, especially in
acid, and therefore forms many erosional
landforms. These include limestone
pavements, pot holes, cenotes, caves and
gorges. Such erosion landscapes are known
as karsts. Limestone is less resistant to
erosion than most igneous rocks, but more
resistant than most other sedimentary
rocks. It is therefore usually associated
with hills and downland, and occurs in
regions with other sedimentary rocks,
typically clays.[83][84]
The Cudgel of Hercules, a The Samulá cenote in
Karst regions overlying limestone bedrock
tall limestone rock in Poland Valladolid, Yucatán, Mexico
(Pieskowa Skała Castle in tend to have fewer visible above-ground
the background) sources (ponds and streams), as surface
water easily drains downward through 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. Most cave systems are through limestone bedrock. Cooling groundwater or mixing of
different groundwaters will also create conditions suitable for cave formation.[83]
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.[85]
Bands of limestone emerge from the Earth's surface in often spectacular rocky outcrops and islands.
Examples include the Rock of Gibraltar,[86] the Burren in County Clare, Ireland;[87] Malham Cove in
North Yorkshire and the Isle of Wight,[88] England; the Great Orme in Wales;[89] on Fårö near the
Swedish island of Gotland,[90] the Niagara Escarpment in Canada/United States;[91] Notch Peak in
Utah;[92] the Ha Long Bay National Park in Vietnam;[93] and the hills around the Lijiang River and
Guilin city in China.[94]
The Florida Keys, islands off the south coast of Florida, are composed mainly of 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.[95]
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Unique habitats are found on alvars, 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.[96] Another
area with large quantities of limestone is the island of Gotland, Sweden.[97] Huge quarries in
northwestern Europe, such as those of Mount Saint Peter (Belgium/Netherlands), extend for more
than a hundred kilometers.[98]
Uses
Limestone is a raw material that is used globally in a variety of
different ways including construction, agriculture and as
industrial materials.[100] Limestone is very common in
architecture, especially in Europe and North America. Many
landmarks across the world, including the Great Pyramid and its
associated 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'.[101] Limestone, metamorphosed by heat and pressure The Megalithic Temples of Malta
such as Ħaġar Qim are built entirely
produces marble, which has been used for many statues,
of limestone. They are among the
buildings and stone tabletops.[102] On the island of Malta, a
oldest freestanding structures in
variety of limestone called Globigerina limestone was, for a long
existence.[99]
time, the only building material available, and is still very
frequently used on all types of buildings and sculptures.[103]
Limestone can be processed into many various forms such as brick, cement, powdered/crushed, or as
a filler.[104] Limestone is readily available and relatively easy to cut into blocks or more elaborate
carving.[99] 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 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.[105] 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[106]), 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. Train stations, banks and other structures from that
era were normally made of limestone. It is used as a facade on
some skyscrapers, but only in thin plates for covering, rather
than solid blocks. In the United States, Indiana, most notably the
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 Odessa in Ukraine in the 19th century were mostly
The Great Pyramid of Giza, one of
constructed from limestone and the extensive remains of the the Seven Wonders of the Ancient
mines now form the Odessa Catacombs.[107] World had an outside cover made
entirely from limestone.
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.[108]
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Limestone is used
worldwide as
building material.
It is the raw material for the manufacture of quicklime (calcium oxide), slaked lime (calcium
hydroxide), cement and mortar.[57]
Pulverized limestone is used as a soil conditioner to neutralize acidic soils (agricultural lime).[114]
Is crushed for use as aggregate—the solid base for many roads as well as in asphalt concrete.[57]
As a reagent in flue-gas desulfurization, where it reacts with sulfur dioxide for air pollution
control.[115]
In glass making, particularly in the manufacture of soda-lime glass.[116]
As an additive toothpaste, paper, plastics, paint, tiles, and other materials as both white pigment
and a cheap filler.[117]
To suppress methane explosions in underground coal mines.[118]
Purified, it is added to bread and cereals as a source of calcium.[119]
As a calcium supplement in livestock feed, such as for poultry (when ground up).[120]
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For remineralizing and increasing the alkalinity of purified water to prevent pipe corrosion and to
restore essential nutrient levels.[121]
In blast furnaces, limestone binds with silica and other impurities to remove them from the
iron.[122]
It can aid in the removal of toxic components created from coal burning plants and layers of
polluted molten metals. [123]
Many limestone formations are porous and permeable, which makes them important petroleum
reservoirs.[124] About 20% of North American hydrocarbon reserves are found in carbonate rock.
Carbonate reservoirs are very common in the petroleum-rich Middle East,[57] and carbonate
reservoirs hold about a third of all petroleum reserves worldwide.[125] 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.[57]
Scarcity
Limestone is a huge industrial material that is in constant demand. This raw material was and has
been essential in the iron and steel industry since the nineteenth century.[126] Companies never had a
shortage of limestone, however it was a concern as the demand continued to increase[127] and in fact
is still in high demand today.[128] The major potential threats back in the nineteenth century were
regional availability and accessibility.[126] 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.[129] These two dominant factors lead
to the adaptation and selection of other materials that were created and formed to design alternatives
for limestone that suited economic demands.[126]
Limestone was classified as a critical raw material however, 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 and granted a significant impact to the construction of new
substances, minette ores is a common substitute for example.[126]
United States
The Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible
exposure limit) for limestone exposure in the workplace as 15 mg/m3 total exposure and 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 10 mg/m3 total exposure and
5 mg/m3 respiratory exposure over an 8-hour workday.[132]
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Graffiti
Removing graffiti from weathered limestone is difficult because it is a porous and permeable
material. The surface is fragile so usual abrasion methods run the risk of severe surface loss. Because
it is an acid-sensitive stone some cleaning agents cannot be used due to adverse effects.[133]
Gallery
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Chalk is a variety of
limestone. It is a
softer, and more
powdery material.
See also
Coral sand
In Praise of Limestone – poem by W. H. Auden
Kurkar – Regional name for an aeolian quartz calcrete on the Levantine coast
Limepit – Old method of calcining limestone
Sandstone – Type of sedimentary rock
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Further reading
Boynton, Robert S. (1980). Chemistry and Technology of Lime and Limestone (https://archive.org/
details/rulesdistrictco00distgoog). Wiley. ISBN 0471027715.
https://en.wikipedia.org/wiki/Limestone 21/21