Isotope fractionation in the context of Stable isotope


Isotope fractionation in the context of Stable isotope

Isotope fractionation Study page number 1 of 1

Play TriviaQuestions Online!

or

Skip to study material about Isotope fractionation in the context of "Stable isotope"


⭐ Core Definition: Isotope fractionation

Isotope fractionation describes fractionation processes that affect the relative abundance of isotopes, a phenomenon that occurs (and so advantage is taken of it) in the study geochemistry, biochemistry, food science, and other fields. Normally, the focus is on stable isotopes of the same element. Isotopic fractionation can be measured by isotope analysis, using isotope-ratio mass spectrometry, nuclear magnetic resonance methods (specialised techniques,) cavity ring-down spectroscopy, etc., to measure ratios of isotopes, important tools to understand geochemical and biological systems, past and present. For example, biochemical processes cause changes in ratios of stable carbon isotopes incorporated into biomass.

↓ Menu
HINT:

In this Dossier

Isotope fractionation in the context of Stable isotope ratio

The term stable isotope has a meaning similar to stable nuclide, but is preferably used when speaking of nuclides of a specific element. Hence, the plural form stable isotopes usually refers to isotopes of the same element. The relative abundance of such stable isotopes can be measured experimentally (isotope analysis), yielding an isotope ratio that can be used as a research tool. Theoretically, such stable isotopes could include the radiogenic daughter products of radioactive decay, used in radiometric dating. However, the expression stable-isotope ratio is preferably used to refer to isotopes whose relative abundances are affected by isotope fractionation in nature. This field is termed stable isotope geochemistry.

View the full Wikipedia page for Stable isotope ratio
↑ Return to Menu

Isotope fractionation in the context of Oxygen isotope ratio cycle

Oxygen isotope ratio cycles are cyclical variations in the ratio of the abundance of oxygen with an atomic mass of 18 to the abundance of oxygen with an atomic mass of 16 present in some substances, such as polar ice or calcite in ocean core samples, measured with the isotope fractionation. The ratio is linked to ancient ocean temperature which in turn reflects ancient climate. Cycles in the ratio mirror climate changes in the geological history of Earth.

View the full Wikipedia page for Oxygen isotope ratio cycle
↑ Return to Menu

Isotope fractionation in the context of Isotope geochemistry

Isotope geochemistry is an aspect of geology based upon the study of natural variations in the relative abundances of isotopes of various elements. Variations in isotopic abundance are measured by isotope-ratio mass spectrometry, and can reveal information about the ages and origins of rock, air or water bodies, or processes of mixing between them.

Stable isotope geochemistry is largely concerned with isotopic variations arising from mass-dependent isotope fractionation, whereas radiogenic isotope geochemistry is concerned with the products of natural radioactivity.

View the full Wikipedia page for Isotope geochemistry
↑ Return to Menu

Isotope fractionation in the context of Reference Materials for Stable Isotope Analysis

Isotopic reference materials are compounds (solids, liquids, gasses) with well-defined isotopic compositions and are the ultimate sources of accuracy in mass spectrometric measurements of isotope ratios. Isotopic references are used because mass spectrometers are highly fractionating. As a result, the isotopic ratio that the instrument measures can be very different from that in the sample's measurement. Moreover, the degree of instrument fractionation changes during measurement, often on a timescale shorter than the measurement's duration, and can depend on the characteristics of the sample itself. By measuring a material of known isotopic composition, fractionation within the mass spectrometer can be removed during post-measurement data processing. Without isotope references, measurements by mass spectrometry would be much less accurate and could not be used in comparisons across different analytical facilities. Due to their critical role in measuring isotope ratios, and in part, due to historical legacy, isotopic reference materials define the scales on which isotope ratios are reported in the peer-reviewed scientific literature.

Isotope reference materials are generated, maintained, and sold by the International Atomic Energy Agency (IAEA), the National Institute of Standards and Technology (NIST), the United States Geologic Survey (USGS), the Institute for Reference Materials and Measurements (IRMM), and a variety of universities and scientific supply companies. Each of the major stable isotope systems (hydrogen, carbon, oxygen, nitrogen, and sulfur) has a wide variety of references encompassing distinct molecular structures. For example, nitrogen isotope reference materials include N-bearing molecules such ammonia (NH3), atmospheric dinitrogen (N2), and nitrate (NO3). Isotopic abundances are commonly reported using the δ notation, which is the ratio of two isotopes (R) in a sample relative to the same ratio in a reference material, often reported in per mille (‰) (equation below). Reference material span a wide range of isotopic compositions, including enrichments (positive δ) and depletions (negative δ). While the δ values of references are widely available, estimates of the absolute isotope ratios (R) in these materials are seldom reported. This article aggregates the δ and R values of common and non-traditional stable isotope reference materials.

View the full Wikipedia page for Reference Materials for Stable Isotope Analysis
↑ Return to Menu