Lysocline

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The graphic presents the present-day annual mean surface omega calcite: the normalised saturation state of calcite. Areas with a value less an 1 indicate a likeliness for dissolution (undersaturated) while a value over 1 indicates areas less likely for dissolution (oversaturation). Surface ocean present-day omega calcite, GLODAPv2.png
The graphic presents the present-day annual mean surface omega calcite: the normalised saturation state of calcite. Areas with a value less an 1 indicate a likeliness for dissolution (undersaturated) while a value over 1 indicates areas less likely for dissolution (oversaturation).

The lysocline is the depth in the ocean dependent upon the carbonate compensation depth (CCD), usually around 5 km, below which the rate of dissolution of calcite increases dramatically because of a pressure effect. While the lysocline is the upper bound of this transition zone of calcite saturation, the CCD is the lower bound of this zone. [1]

Contents

CaCO3 content in sediment varies with different depths of the ocean, spanned by levels of separation known as the transition zone. In the mid-depth area of the ocean, sediments are rich in CaCO3, content values reaching 85–95%. [1] This area is then spanned hundreds of meters by the transition zone, ending in the abyssal depths with 0% concentration. The lysocline is the upper bound of the transition zone, where amounts of CaCO3 content begins to noticeably drop from the mid-depth 85–95% sediment. The CaCO3 content drops to 0% concentration at the lower bound, known as the calcite compensation depth. [1]

Shallow marine waters are generally supersaturated in calcite, CaCO3, because as marine organisms (which often have shells made of calcite or its polymorph, aragonite) die, they tend to fall downwards without dissolving. [2] As depth and pressure increases within the water column, calcite solubility increases, causing supersaturated water above the saturation depth, allowing for preservation and burial of CaCO3 on the seafloor. [3] However, this creates undersaturated seawater below the saturation depth, preventing CaCO3 burial on the sea floor as the shells start to dissolve.

The equation Ω = [Ca2+] X [CO32-]/K'sp expresses the CaCO3 saturation state of seawater. [4] The calcite saturation horizon is where Ω =1; dissolution proceeds slowly below this depth. The lysocline is the depth that this dissolution impacts is again notable, also known as the inflection point with sedimentary CaCO3 versus various water depths. [4]

Calcite compensation depth

The calcite compensation depth (CCD) occurs at the depth that the rate of calcite to the sediments is balanced with the dissolution flux, the depth at which the CaCO3 content are values 2–10%. [4] Hence, the lysocline and CCD are not equivalent. The lysocline and compensation depth occur at greater depths in the Atlantic (5000–6000 m) than in the Pacific (4000–5000 m), and at greater depths in equatorial regions than in polar regions. [5]

The depth of the CCD varies as a function of the chemical composition of the seawater and its temperature. [6] Specifically, it is the deep waters that are undersaturated with calcium carbonate primarily because its solubility increases strongly with increasing pressure and salinity and decreasing temperature. As the atmospheric concentration of carbon dioxide continues to increase, the CCD can be expected to decrease in depth, as the ocean's acidity rises. [3]

See also

Related Research Articles

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Limestone is a type of carbonate sedimentary rock which is the main source of the material lime. It is composed mostly of the minerals calcite and aragonite, which are different crystal forms of 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, such as the accumulation of corals and shells in the sea, have likely been more important for the last 540 million years. Limestone often contains fossils which provide scientists with information on ancient environments and on the evolution of life.

<span class="mw-page-title-main">Coccolithophore</span> Unicellular algae responsible for the formation of chalk

Coccolithophores, or coccolithophorids, are single-celled organisms which are part of the phytoplankton, the autotrophic (self-feeding) component of the plankton community. They form a group of about 200 species, and belong either to the kingdom Protista, according to Robert Whittaker's five-kingdom system, or clade Hacrobia, according to a newer biological classification system. Within the Hacrobia, the coccolithophores are in the phylum or division Haptophyta, class Prymnesiophyceae. Coccolithophores are almost exclusively marine, are photosynthetic, and exist in large numbers throughout the sunlight zone of the ocean.

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<span class="mw-page-title-main">Dolomite (rock)</span> Sedimentary carbonate rock that contains a high percentage of the mineral dolomite

Dolomite (also known as dolomite rock, dolostone or dolomitic rock) is a sedimentary carbonate rock that contains a high percentage of the mineral dolomite, CaMg(CO3)2. It occurs widely, often in association with limestone and evaporites, though it is less abundant than limestone and rare in Cenozoic rock beds (beds less than about 66 million years in age). The first geologist to distinguish dolomite from limestone was Déodat Gratet de Dolomieu; a French mineralogist and geologist whom it is named after. He recognized and described the distinct characteristics of dolomite in the late 18th century, differentiating it from limestone.

<span class="mw-page-title-main">Alkalinity</span> Capacity of water to resist changes in pH that would make the water more acidic

Alkalinity (from Arabic: القلوية, romanized: al-qaly, lit. 'ashes of the saltwort') is the capacity of water to resist acidification. It should not be confused with basicity, which is an absolute measurement on the pH scale. Alkalinity is the strength of a buffer solution composed of weak acids and their conjugate bases. It is measured by titrating the solution with an acid such as HCl until its pH changes abruptly, or it reaches a known endpoint where that happens. Alkalinity is expressed in units of concentration, such as meq/L (milliequivalents per liter), μeq/kg (microequivalents per kilogram), or mg/L CaCO3 (milligrams per liter of calcium carbonate). Each of these measurements corresponds to an amount of acid added as a titrant.

<span class="mw-page-title-main">Carbonate rock</span> Class of sedimentary rock

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<span class="mw-page-title-main">Authigenesis</span>

Authigenesis is the process whereby a mineral or sedimentary rock deposit is generated where it is found or observed. Such deposits are described as authigenic. Authigenic sedimentary minerals form during or after sedimentation by precipitation or recrystallization as opposed to detrital minerals, which are weathered by water or wind and transported to the depositional location. Authigenic sediments are the main constituents of deep sea sedimentation, compared to shallow waters or land where detrital sediments are more common.

<span class="mw-page-title-main">Marine sediment</span>

Marine sediment, or ocean sediment, or seafloor sediment, are deposits of insoluble particles that have accumulated on the seafloor. These particles have their origins in soil and rocks and have been transported from the land to the sea, mainly by rivers but also by dust carried by wind and by the flow of glaciers into the sea. Additional deposits come from marine organisms and chemical precipitation in seawater, as well as from underwater volcanoes and meteorite debris.

<span class="mw-page-title-main">Calcite sea</span> Sea chemistry favouring low-magnesium calcite as the inorganic calcium carbonate precipitate

A calcite sea is a sea in which low-magnesium calcite is the primary inorganic marine calcium carbonate precipitate. An aragonite sea is the alternate seawater chemistry in which aragonite and high-magnesium calcite are the primary inorganic carbonate precipitates. The Early Paleozoic and the Middle to Late Mesozoic oceans were predominantly calcite seas, whereas the Middle Paleozoic through the Early Mesozoic and the Cenozoic are characterized by aragonite seas.

<span class="mw-page-title-main">Aragonite sea</span> Chemical conditions of the sea favouring aragonite deposition

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References

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