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Remineralization (of Organic Matter)[edit]

In biogeochemistry, remineralization (US Spelling; UK remineralisation) generally refers to the breakdown/transformation of organic matter (those molecules derived from a biological source) into its simplest inorganic forms. These transformations form a crucial link within ecosystems as they are responsible for 1) liberating the energy stored in organic molecules, 2)recycling matter within the system to be reused as nutrients by other organisms.[1]

Remineralization is normally viewed as it relates to the cycling of the major biologically-important elements such as carbon, nitrogen and phosphorus. While crucial to all ecosystems, the process receives special consideration in aquatic settings, where it forms a significant link in the biogeochemical dynamics and cycling of most aquatic ecosystems.

Role in Biogeochemistry[edit]

The term "remineralization" is used in several contexts across different disciplines. It is most commonly used in the medicinal and physiological fields, where it is describes the development or redevelopment of mineralized structures in organisms such as teeth or bone. In the field of biogeochemistry, however, remineralization is used to describe a link in the chain of elemental cycling within a particular ecosystem. In particular, remineralization represents the point where organic material constructed by living organisms is broken down into basal inorganic components that are not obviously identifiable as having come from an organic source. This differs from the process of decomposition in which is a more general descriptor of larger structures degrading to smaller structures.

Biogeochemists study this process across all ecosystems for a variety of reasons. This is done primarily to investigate the flow of material and energy in a given system, which is key to understanding the productivity of that ecosystem along with how it recycles material versus how much is entering the system. Understanding the rates and dynamics of organic matter remineralization in a given system can help in determining how or why some ecosystems might be more productive than others.

Remineralization Reactions[edit]

While it is important to note that the process of remineralization is a series of complex biochemical pathways [within microbes], it can often be simplified as a series of one-step processes for ecosystem-level models and calculations. A generic form of these reactions is shown by:

The above generic equation starts with two reactants: some piece of organic matter (composed of organic carbon) and an oxidant. Most organic carbon exists in a reduced form which is then oxidized by the oxidant (such as O2) into carbon dioxide and energy that can be harnessed by the organism. This process generally produces CO2, water and a collection of simple nutrients like nitrate or phosphate that can then be taken up by other organisms. The above general form, when considering O2 as the oxidant, is the equation for respiration. In this context specifically, the above equation represents bacterial respiration though the reactants and products are essentially analogous to the short-hand equations used for multi-cellular respiration.

Figure 1: Major electron acceptors in marine sediments based on idealized depth in  marine sediments.

Electron Acceptor Cascade[2][edit]

The degradation of organic matter through respiration in the modern ocean is facilitated by different electron acceptors, their favorability based on Gibbs free energy law, and the laws of thermodynamics.  This redox chemistry is the basis for life in deep sea sediments and determines the obtainability of energy to organisms that live there.  From the water interface moving toward deeper sediments, the order of these acceptors is oxygen, nitrate, manganese, iron, and sulfate.  The zonation of these favored acceptors can be seen in Figure 1.  Moving downwards from the surface through the zonation of these deep ocean sediments, acceptors are used and depleted.  Once depleted the next acceptor of lower favorability takes its place.  Thermodynamically, oxygen represents the most favorable electron accepted but is quickly used up in the water sediment interface and O2 concentrations extends only millimeters to centimeters down into the sediment in most locations of the deep sea.  This favorability indicates an organism's ability to obtain higher energy from the reaction which helps them complete with other organisms.[3]  In the absence of these acceptors, organic matter can also be degraded through methanogenesis, but the net oxidation of this organic matter is not fully represented by this process.  Each pathway and the stoichiometry of its reaction are listed in table 1 (Needs to be added).[3]

Due to this quick depletion of O2 in the surface sediments, a majority of microbes use anaerobic pathways to metabolize other oxides such as manganese, iron, and sulfate.[4]  It is also important to figure in bioturbation and the constant mixing of this material which can change the relative importance of each respiration pathway.  For the microbial perspective please reference the electron transport chain.

Remineralization in Sediments[edit]

Reactions[edit]

A quarter of all organic material that exits the photic zone makes it to the seafloor without being remineralized and 90% of that remaining material is remineralized in sediments itself.[1] Once in the sediment, organic remineralization may occur through a variety of reactions.[5] The following reactions are the primary ways in which organic matter is remineralized, where .[6]

Aerobic Respiration[edit]

Aerobic respiration is the most preferred remineralization reaction due to its high energy yield. Although oxygen is quickly depleted in the sediments and is generally exhausted centimeters from the sediment-water interface.

Anerobic Respiration[edit]

In instances in which the environment is suboxic or anoxic, organisms will prefer to utilize denitrification to remineralize organic matter as it provides the second largest amount of energy. In depths below where denitrification is favored, reactions such as Manganese Reduction, Iron Reduction, Sulfate Reduction, Methane Reduction (also known as Methanogenesis), become favored respectively. This favorability is governed by Gibbs Free Energy (ΔG).

Reaction GFE
Aerobic Respiration Oxygen Reduction -29.9
Anerobic Respiration Denitrification -28.4
Manganese Reduction -7.2
Iron Reduction -21.0
Sulfate Reduction -6.1
Methane Fermentation (Methanogenesis) -5.6

Redox Zonation[edit]

Redox zonation refers to how the processes that transfer terminal electrons as a result of organic matter degradation vary depending on time and space.[7] Certain reactions will be favored over others due to their energy yield as detailed in the energy acceptor cascade detailed above.[8] In oxic conditions, in which oxygen is readily available, aerobic respiration will be favored due to its high energy yield. Once the use of oxygen through respiration exceeds the input of oxygen due to bioturbation and diffusion, the environment will become anoxic and organic matter will be broken down via other means, such as denitrification and manganese reduction.[9]

Remineralization in the Water Column[edit]

Food web showing the flow of carbon in the open ocean.

In most pelagic locations, only a small fraction of carbon and other nutrients fixed during primary production at the surface reaches the sea floor. What that fraction is varies depending on the location of interest. For example, in the North Sea, values of carbon deposition is ~1% of primary production[10] while that value is <0.5% in the open oceans on average.[11]  Therefore, most of nutrients remain in the water column, recycled by the biota. Heterotrophic organisms will utilize the materials produced by the autotrophic (and chemotrophic) organisms and via respiration will remineralize the compounds from the organic form back to inorganic, making them available for primary producers again.

For most areas of the ocean, the highest rates of carbon remineralization occur at depths between 100-1200m in the water column, decreasing down to about 1200m where remineralization rates remain pretty constant at 0.1 µmol kg-1 yr-1.[12] This provides the most nutrients available for primary producers within the photic zone [13] though it leaves the upper surface waters starved of inorganic nutrients.

Most remineralization is done with dissolved inorganic carbon (DOC). Studies have shown that it is larger sinking particles that transport matter down to the sea floor [14] while suspended particles and dissolved organics are mostly consumed by remineralization.[15] This happens in part due to the fact that organisms must typically ingest nutrients smaller than they are, often by orders of magnitude.[16] With the microbial community making up 90% of marine biomass[17], it is particles smaller than the microbes (on the order of 10-6 [18]) that will be taken up for remineralization.

See Also[edit]

  1. ^ a b Sarmiento, Jorge (2006). Ocean Biogeochemical Dynamics. Princeton University Press. ISBN 0691017077.
  2. ^ Vernberg, F. John. "Benthic Macrofauna." Functional Adaptations of Marine Organisms (1981): 179-230. Web.
  3. ^ a b Altenbach, Alexander; Bernhard, Joan M.; Seckbach, Joseph (2011-10-20). Anoxia: Evidence for Eukaryote Survival and Paleontological Strategies. Springer Science & Business Media. ISBN 9789400718968.
  4. ^ Glud, Ronnie (2008). "Oxygen dynamics of marine sediments" (PDF). Marine Biology Research.
  5. ^ Burdige, David (2006). Geochemistry of Marine Sediments. Princeton University Press. ISBN 069109506X.
  6. ^ Anderson, Laurence A.; Sarmiento, Jorge L. (1994-03-01). "Redfield ratios of remineralization determined by nutrient data analysis". Global Biogeochemical Cycles. 8 (1): 65–80. doi:10.1029/93GB03318. ISSN 1944-9224.
  7. ^ Postma, Dieke; Jakobsen, Rasmus (1996-09-01). "Redox zonation: Equilibrium constraints on the Fe(III)/SO4-reduction interface". Geochimica et Cosmochimica Acta. 60 (17): 3169–3175. doi:10.1016/0016-7037(96)00156-1.
  8. ^ Boudreau, Bernard (2001). The Benthic Boundary Layer: Transport Processes and Biogeochemistry. Oxford University Press. ISBN 0195118812.
  9. ^ Libes, Susan (2009). Introduction to Marine Biogeochemistry. Academic Press. ISBN 0120885301.
  10. ^ Thomas, Helmuth; Bozec, Yann; Elkalay, Khalid; Baar, Hein J. W. de (2004-05-14). "Enhanced Open Ocean Storage of CO2 from Shelf Sea Pumping". Science. 304 (5673): 1005–1008. doi:10.1126/science.1095491. ISSN 0036-8075. PMID 15143279.
  11. ^ De La Rocha, CL (2006). "The Biological Pump. In: Treatise on Geochemistry". Pergamon press. doi:vol 6. {{cite journal}}: Check |doi= value (help)
  12. ^ Feely, Richard A.; Sabine, Christopher L.; Schlitzer, Reiner; Bullister, John L.; Mecking, Sabine; Greeley, Dana (2004-02-01). "Oxygen Utilization and Organic Carbon Remineralization in the Upper Water Column of the Pacific Ocean". Journal of Oceanography. 60 (1): 45–52. doi:10.1023/B:JOCE.0000038317.01279.aa. ISSN 0916-8370.
  13. ^ Administration, US Department of Commerce, National Oceanic and Atmospheric. "How far does light travel in the ocean?". oceanservice.noaa.gov. Retrieved 2016-02-29.{{cite web}}: CS1 maint: multiple names: authors list (link)
  14. ^ Karl, David M.; Knauer, George A.; Martin, John H. (1988-03-01). "Downward flux of particulate organic matter in the ocean: a particle decomposition paradox". Nature. 332: 438–441. doi:10.1038/332438a0. ISSN 0028-0836.
  15. ^ Lefévre, D.; Denis, M.; Lambert, C. E.; Miquel, J. -C. (1996-02-01). "Is DOC the main source of organic matter remineralization in the ocean water column?". Journal of Marine Systems. The Coastal Ocean in a Global Change Perspective. 7 (2–4): 281–291. doi:10.1016/0924-7963(95)00003-8.
  16. ^ Schulze, Ernst-Detlef; Mooney, Harold A. (2012-12-06). Biodiversity and Ecosystem Function. Springer Science & Business Media. ISBN 9783642580017.
  17. ^ "International Census of Marine Microbes (ICoMM) | Census of Marine Life". www.coml.org. Retrieved 2016-02-29.
  18. ^ "Microbe Size - Boundless Open Textbook". Boundless. Retrieved 2016-02-29.