Chemistry:Lysocline
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 boundary of this calcite saturation transition zone, the CCD is its lower boundary.[1]
CaCO3 content in sediment varies with ocean depth, spanning levels of separation known as the transition zone. In the mid-depth areas of the ocean, sediments are rich in calcium carbonate, with CaCO3 content reaching 85–95%.[1] This area is then spanned by the transition zone for hundreds of meters, ending in the abyssal depths at a concentration of 0%. The lysocline is the upper boundary of the transition zone, where CaCO3 content begins to drop noticeably from the mid-depth 85–95% sediment. The CaCO3 content drops to 0% concentration at the lower boundary, 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 seafloor as the shells start to dissolve.
The calcium carbonate dissolution/precipitation equilibrium is governed by the law of mass action and the Le Chatelier's principle as follows:
The CaCO
3 solubility product () corresponds to the ion-activity product (IAP, or Q) at chemical equilibrium:
- at chemical equilibrium
The CaCO3 saturation state of seawater can be expressed in terms of or with the help of saturation index ().[4]
The saturation index () is defined as the decimal logarithm of spanning several orders of magnitude:
The calcite saturation horizon is where Ω = 1, or SI = 0. Above this depth, seawater can be supersaturated with respect to CaCO
3 (Ω > 1, or SI > 0). As seawater becomes undersaturated below this depth (Ω < 1, or SI < 0), calcium carbonate dissolution proceeds slowly. The lysocline is the depth at which this dissolution becomes notable again, also known as the inflexion point in the relationship between sedimentary CaCO3 and water depth.[4]
Calcite compensation depth
The calcite compensation depth (CCD) is the depth at which the rate of calcite input to the sediments is balanced by the dissolution flux, typically at a CaCO3 content of 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 with seawater chemical composition and 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
References
- ↑ 1.0 1.1 1.2 Broecker, W. S. (2003). "6.19 – The Oceanic CaCO3 Cycle". in Holland, Heinrich D.; Turekian, Karl K.. Treatise on Geochemistry. Pergamon. pp. 529–549. doi:10.1016/b0-08-043751-6/06119-3. ISBN 9780080437514. http://www.sciencedirect.com/science/article/pii/B0080437516061193. Retrieved 2019-10-17.
- ↑ Shiraiwa, Y. (2003). "Physiological regulation of carbon fixation in the photosynthesis and calcification of coccolithophorids". Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 136 (4): 775–783. doi:10.1016/S1096-4959(03)00221-5. ISSN 1096-4959. PMID 14662302.
- ↑ 3.0 3.1 Sigman, D. M.; Boyle, E. A. (2000). "Glacial/interglacial variations in atmospheric carbon dioxide" (in en). Nature 407 (6806): 859–869. doi:10.1038/35038000. ISSN 1476-4687. PMID 11057657. Bibcode: 2000Natur.407..859S.
- ↑ 4.0 4.1 4.2 Zeebe, R. E. (2012). "History of Seawater Carbonate Chemistry, Atmospheric CO2, and Ocean Acidification". Annual Review of Earth and Planetary Sciences 40 (1): 141–165. doi:10.1146/annurev-earth-042711-105521. ISSN 0084-6597. Bibcode: 2012AREPS..40..141Z.
- ↑ Volat, J. L.; Pastouret, L.; V. G., Colette (1980). "Dissolution and carbonate fluctuations in Pleistocene deep-sea cores: A review". Marine Geology 34 (1): 1–28. doi:10.1016/0025-3227(80)90138-3. ISSN 0025-3227. Bibcode: 1980MGeol..34....1V.
- ↑ Broecker, W. S. (2009). "Wally's Quest to Understand the Ocean's CaCO3 Cycle". Annual Review of Marine Science 1 (1): 1–18. doi:10.1146/annurev.marine.010908.163936. ISSN 1941-1405. PMID 21141027. Bibcode: 2009ARMS....1....1B.
