Iodine cycle

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Biogeochemical iodine cycle: Inventories are in Tg iodine per year. Labeled flux arrows are in Gg iodine per year. Unlabeled inventories (sinks) and fluxes are of unknown quantities. Iodine cycles through the lithosphere, atmosphere, hydrosphere, and biosphere. Freshwater iodine is calculated by subtracting oceanic iodine from total iodine in the hydrosphere. In oceans sediments and crust, iodine is replenished by sedimentation and is cycled into seawater through release as brine during subduction. Marine biota uptake iodine from seawater where it may be volatilized by transformation to methyl iodide. Sea spray aerosolization, volcanic activity, and fossil fuel burning cycles iodine from the hydrosphere and lithosphere into the atmosphere as well, while wet and dry deposition remove iodine from the atmosphere. In soil, small quantities of iodine are cycled through weathering of parent rock. Terrestrial biota uptake and remove iodine from soil, and bacteria volatilize iodine by methylizing it. Iodine Figure Draft 1.png
Biogeochemical iodine cycle: Inventories are in Tg iodine per year. Labeled flux arrows are in Gg iodine per year. Unlabeled inventories (sinks) and fluxes are of unknown quantities. Iodine cycles through the lithosphere, atmosphere, hydrosphere, and biosphere. Freshwater iodine is calculated by subtracting oceanic iodine from total iodine in the hydrosphere. In oceans sediments and crust, iodine is replenished by sedimentation and is cycled into seawater through release as brine during subduction. Marine biota uptake iodine from seawater where it may be volatilized by transformation to methyl iodide. Sea spray aerosolization, volcanic activity, and fossil fuel burning cycles iodine from the hydrosphere and lithosphere into the atmosphere as well, while wet and dry deposition remove iodine from the atmosphere. In soil, small quantities of iodine are cycled through weathering of parent rock. Terrestrial biota uptake and remove iodine from soil, and bacteria volatilize iodine by methylizing it.

The iodine cycle is a biogeochemical cycle that primarily consists of natural [1] and biological processes [3] that exchange iodine through the lithosphere, hydrosphere, and atmosphere. [3] [2] Iodine exists in many forms, but in the environment, it generally has an oxidation state of -1, 0, or +5. [1]

Contents

Oceanic cycling

Iodine in the ocean exists mostly in oceanic sediments and seawater. [4] During subduction of oceanic crust and seawater, most of the iodine cycles into seawater through brine, while a minor amount is cycled into the mantle. [4] Marine biota, including seaweed and fish, accumulate iodine from the seawater and return it during decomposition. [2] Sedimentation of oceanic iodine replenishes the ocean sediment sink. [1]

The losses of iodine from the oceanic sink are to the atmospheric sink. [1] Sea spray aerosolization accounts for a portion of this loss. [2] However, the majority of the iodine cycled into the atmosphere occurs through biological conversion of iodide and iodate to methyl forms, primarily methyl iodide. [3] Algae, phytoplankton, and bacteria are involved in reducing the stable Iodate ion to iodide, [5] and different species produce volatile methyl iodide which leaves the oceans and forms aerosols in the atmosphere. [3]

Terrestrial cycling

Iodine rarely occurs naturally in mineral form, so it comprises a very small portion of rocks by mass. [2] Sedimentary rocks have higher concentrations of iodine compared to metamorphic and igneous rocks. [4] Due to the low concentration of iodine in rocks, weathering is a minor flux of iodine to soils and the freshwater hydrosphere. [1]

Soils contain a much higher concentration of iodine compared to their parent rock, though most of it is bound to organic and inorganic matter, potentially due to microbial activity. [4] The major source of iodine to soils is through dry and wet deposition of aerosolized iodine in the atmosphere. [1] Due to the high production of atmospheric iodine from the oceans, both the concentration of iodine and the flux of iodine to soils is greatest near coastal regions. [1] Plants uptake iodine from the soil through their roots and return the iodine when they decompose. [2] Fauna that consume plants may uptake this iodine but similarly return it to soils upon decomposition. [2] Some iodine may also be cycled into the freshwater hydrosphere through leaching and runoff, where it may return to the oceans. [1]

Similar to oceanic iodine, the majority of iodine cycled out of soil is volatilized through conversion to methyl forms of iodine by bacteria. [3] Unlike ocean volatilization, however, bacteria are thought to be the only organisms responsible for volatilization in soils. [4]

Anthropogenic influences

Iodine is a necessary trace nutrient for human health and is used as a product for various industries. [3] Iodine intended for human use and consumption is taken from brines, which accounts for a minor perturbation to the global iodine cycle. [1] A much larger anthropogenic impact is through the burning of fossil fuels, which releases iodine into the atmosphere. [1]

Iodine-129, a radioisotope of iodine, is a waste product of nuclear power generation and weapons testing. [3] Unless present in high concentrations, I-129 likely does not present danger to human health. [6] Early research has attempted to use the I-129/I-127 ratio as a tracer for the iodine cycle. [6]

Related Research Articles

<span class="mw-page-title-main">Iodine</span> Chemical element, symbol I and atomic number 53

Iodine is a chemical element; it has symbol I and atomic number 53. The heaviest of the stable halogens, it exists at standard conditions as a semi-lustrous, non-metallic solid that melts to form a deep violet liquid at 114 °C (237 °F), and boils to a violet gas at 184 °C (363 °F). The element was discovered by the French chemist Bernard Courtois in 1811 and was named two years later by Joseph Louis Gay-Lussac, after the Ancient Greek Ιώδης 'violet-coloured'.

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<span class="mw-page-title-main">Iodic acid</span> Chemical compound (HIO3)

Iodic acid is a white water-soluble solid with the chemical formula HIO3. Its robustness contrasts with the instability of chloric acid and bromic acid. Iodic acid features iodine in the oxidation state +5 and is one of the most stable oxo-acids of the halogens. When heated, samples dehydrate to give iodine pentoxide. On further heating, the iodine pentoxide further decomposes, giving a mix of iodine, oxygen and lower oxides of iodine.

<span class="mw-page-title-main">Sulfur cycle</span> Biogeochemical cycle of sulfur

The important sulfur cycle is a biogeochemical cycle in which the sulfur moves between rocks, waterways and living systems. It is important in geology as it affects many minerals and in life because sulfur is an essential element (CHNOPS), being a constituent of many proteins and cofactors, and sulfur compounds can be used as oxidants or reductants in microbial respiration. The global sulfur cycle involves the transformations of sulfur species through different oxidation states, which play an important role in both geological and biological processes. Steps of the sulfur cycle are:

<span class="mw-page-title-main">Briggs–Rauscher reaction</span> Oscillating chemical reaction

The Briggs–Rauscher oscillating reaction is one of a small number of known oscillating chemical reactions. It is especially well suited for demonstration purposes because of its visually striking colour changes: the freshly prepared colourless solution slowly turns an amber colour, then suddenly changes to a very dark blue. This slowly fades to colourless and the process repeats, about ten times in the most popular formulation, before ending as a dark blue liquid smelling strongly of iodine.

<span class="mw-page-title-main">Microbial loop</span> Trophic pathway in marine microbial ecosystems

The microbial loop describes a trophic pathway where, in aquatic systems, dissolved organic carbon (DOC) is returned to higher trophic levels via its incorporation into bacterial biomass, and then coupled with the classic food chain formed by phytoplankton-zooplankton-nekton. In soil systems, the microbial loop refers to soil carbon. The term microbial loop was coined by Farooq Azam, Tom Fenchel et al. in 1983 to include the role played by bacteria in the carbon and nutrient cycles of the marine environment.

<span class="mw-page-title-main">Phosphorus cycle</span> Biogeochemical movement

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Organoiodine chemistry is the study of the synthesis and properties of organoiodine compounds, or organoiodides, organic compounds that contain one or more carbon–iodine bonds. They occur widely in organic chemistry, but are relatively rare in nature. The thyroxine hormones are organoiodine compounds that are required for health and the reason for government-mandated iodization of salt.

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<span class="mw-page-title-main">Boron cycle</span> Biogeochemical cycle

The boron cycle is the biogeochemical cycle of boron through the atmosphere, lithosphere, biosphere, and hydrosphere.

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

The arsenic (As) cycle is the biogeochemical cycle of natural and anthropogenic exchanges of arsenic terms through the atmosphere, lithosphere, pedosphere, hydrosphere, and biosphere. Although arsenic is naturally abundant in the Earth's crust, long-term exposure and high concentrations of arsenic can be detrimental to human health.

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

The chlorine cycle (Cl) is the biogeochemical cycling of chlorine through the atmosphere, hydrosphere, biosphere, and lithosphere. Chlorine is most commonly found as inorganic chloride ions, or a number of chlorinated organic forms. Over 5,000 biologically-produced chlorinated organics have been identified.

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

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

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

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<span class="mw-page-title-main">Manganese cycle</span> Biogeochemical cycle

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References

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  5. Reyes-Umana, Victor; Henning, Zachary; Lee, Kristina; Barnum, Tyler P.; Coates, John D. (2021-07-02). "Genetic and phylogenetic analysis of dissimilatory iodate-reducing bacteria identifies potential niches across the world's oceans". The ISME Journal. 16 (1): 38–49. doi:10.1038/s41396-021-01034-5. ISSN   1751-7370. PMC   8692401 . PMID   34215855.
  6. 1 2 Hou, Xiaolin; Hansen, Violeta; Aldahan, Ala; Possnert, Göran; Lind, Ole Christian; Lujaniene, Galina (2009). "A review on speciation of iodine-129 in the environmental and biological samples". Analytica Chimica Acta. 632 (2): 181–196. doi:10.1016/j.aca.2008.11.013. ISSN   0003-2670. PMID   19110092. S2CID   11740112.