Mass-independent fractionation
Mass-independent (isotope) fractionation refers to any chemical or physical process that acts to separate isotopes, where the amount of separation does not scale in proportion with the difference in the masses of the isotopes. Most isotopic fractionations (including typical kinetic fractionations and equilibrium fractionations) are caused by the effects of the mass of an isotope on atomic or molecular velocities, diffusivities or bond strengths. Mass-independent fractionation processes are less common, occurring mainly in photochemical and spin-forbidden reactions. Observation of mass-independently fractionated materials can therefore be used to trace these types of reactions in nature and in laboratory experiments.
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Mass-independent fractionation in nature
The most notable examples of mass-independent fractionation in nature are found in the isotopes of oxygen and sulfur. The first example was discovered by Robert N. Clayton, Toshiko Mayeda, and Lawrence Grossman in 1973,[1] in the oxygen isotopic composition of refractory calcium-aluminium-rich inclusions in the Allende meteorite. The inclusions, thought to be among the oldest solid materials in the Solar System, show a pattern of low 18O/16O and 17O/16O relative to samples from the Earth and Moon. Both ratios vary by the same amount in the inclusions, although the mass difference between 18O and 16O is almost twice as large as the difference between 17O and 16O. Originally this was interpreted as evidence of incomplete mixing of 16O-rich material (created and distributed by a large star in a supernova) into the Solar nebula. However, recent measurement of the oxygen-isotope composition of the Solar wind, using samples collected by the Genesis spacecraft, shows that the most 16O-rich inclusions are close to the bulk composition of the solar system. This implies that Earth, the Moon, Mars and asteroids all formed from 18O- and 17O-enriched material. Photochemical dissociation of carbon monoxide in the Solar nebula has been proposed to explain this isotope fractionation.
Mass-independent fractionation also has been observed in ozone. Large, 1:1 enrichments of 18O/16O and 17O/16O in ozone were discovered in laboratory synthesis experiments by John Heidenreich and Mark Thiemens in 1983,[2] and later found in stratospheric air samples measured by Konrad Mauersberger.[3] These enrichments were eventually traced to the three-body ozone formation reaction.[4]
- O + O2 → O3* + M → O3 + M*
Theoretical calculations[5] by Rudolph Marcus and others suggest that the enrichments are the result of a combination of mass-dependent and mass-independent kinetic isotope effects (KIE) involving the excited state O3* intermediate related to some unusual symmetry properties. For formation of ozone substituted with a heavy oxygen atom at the terminal position of the molecule, a highly zero-point energy difference sensitive KIE creates large enrichments for the differences in mass between 18O, 17O, and 16O. For formation of ozone substituted with a heavy oxygen atom at the central position of the molecule (or unsubstituted), the relatively short lifetime the O3* intermediate does not allow a statistical distribution of energy throughout all the degrees of freedom, resulting in a mass-independent distribution of isotopes.
Mass-independent sulfur fractionation
Mass-independent fractionation of sulfur can be observed in ancient sediments,[6] where it preserves a signal of the prevailing environmental conditions. The creation and transfer of the mass-independent signature into minerals would be unlikely in an atmosphere containing abundant oxygen, constraining the Great Oxygenation Event to some time after 2,450 million years ago. Prior to this time, the MIS record implies that sulfate-reducing bacteria did not play a significant role in the global sulfur cycle, and that the MIS signal is due primarily to changes in volcanic activity.[7]
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