Isotope geochemistry

Carbon has two stable isotopes, ¹²C and ¹³C, and one radioactive isotope, ¹⁴C.

The stable carbon isotope ratio, δ¹³C, is measured against Vienna Pee Dee Belemnite (VPDB).[2] The stable carbon isotopes are fractionated primarily by photosynthesis (Faure, 2004). The ¹³C/¹²C ratio is also an indicator of paleoclimate: a change in the ratio in the remains of plants indicates a change in the amount of photosynthetic activity, and thus in how favorable the environment was for the plants. During photosynthesis, organisms using the C₃ pathway show different enrichments compared to those using the C₄ pathway, allowing scientists not only to distinguish organic matter from abiotic carbon, but also what type of photosynthetic pathway the organic matter was using.[1] Occasional spikes in the global ¹³C/¹²C ratio have also been useful as stratigraphic markers for chemostratigraphy, especially during the Paleozoic.[3]

The ¹⁴C ratio has been used to track ocean circulation, among other things.

Nitrogen has two stable isotopes, ¹⁴N and ¹⁵N. The ratio between these is measured relative to nitrogen in ambient air.[2] Nitrogen ratios are frequently linked to agricultural activities. Nitrogen isotope data has also been used to measure the amount of exchange of air between the stratosphere and troposphere using data from the greenhouse gas N₂O.[4]

Oxygen has three stable isotopes, ¹⁶O, ¹⁷O, and ¹⁸O. Oxygen ratios are measured relative to Vienna Standard Mean Ocean Water (VSMOW) or Vienna Pee Dee Belemnite (VPDB).[2] Variations in oxygen isotope ratios are used to track both water movement, paleoclimate,[1] and atmospheric gases such as ozone and carbon dioxide.[5] Typically, the VPDB oxygen reference is used for paleoclimate, while VSMOW is used for most other applications.[1] Oxygen isotopes appear in anomalous ratios in atmospheric ozone, resulting from mass-independent fractionation.[6] Isotope ratios in fossilized foraminifera have been used to deduce the temperature of ancient seas.[7]

Sulfur has four stable isotopes, with the following abundances: ³²S (0.9502), ³³S (0.0075), ³⁴S (0.0421) and ³⁶S (0.0002). These abundances are compared to those found in Cañon Diablo troilite.[5] Variations in sulfur isotope ratios are used to study the origin of sulfur in an orebody and the temperature of formation of sulfur–bearing minerals as well as a biosignature that can reveal presence of sulfate reducing microbes.[8][9]

Lead has four stable isotopes: ²⁰⁴Pb, ²⁰⁶Pb, ²⁰⁷Pb, and ²⁰⁸Pb.

Lead is created in the Earth via decay of actinide elements, primarily uranium and thorium.

Lead isotope geochemistry is useful for providing isotopic dates on a variety of materials. Because the lead isotopes are created by decay of different transuranic elements, the ratios of the four lead isotopes to one another can be very useful in tracking the source of melts in igneous rocks, the source of sediments and even the origin of people via isotopic fingerprinting of their teeth, skin and bones.

It has been used to date ice cores from the Arctic shelf, and provides information on the source of atmospheric lead pollution.

Lead–lead isotopes has been successfully used in forensic science to fingerprint bullets, because each batch of ammunition has its own peculiar ²⁰⁴Pb/²⁰⁶Pb vs ²⁰⁷Pb/²⁰⁸Pb ratio.

Samarium–neodymium is an isotope system which can be utilised to provide a date as well as isotopic fingerprints of geological materials, and various other materials including archaeological finds (pots, ceramics).

¹⁴⁷Sm decays to produce ¹⁴³Nd with a half life of 1.06x10¹¹ years.

Dating is achieved usually by trying to produce an isochron of several minerals within a rock specimen. The initial ¹⁴³Nd/¹⁴⁴Nd ratio is determined.

This initial ratio is modelled relative to CHUR (the Chondritic Uniform Reservoir), which is an approximation of the chondritic material which formed the solar system. CHUR was determined by analysing chondrite and achondrite meteorites.

The difference in the ratio of the sample relative to CHUR can give information on a model age of extraction from the mantle (for which an assumed evolution has been calculated relative to CHUR) and to whether this was extracted from a granitic source (depleted in radiogenic Nd), the mantle, or an enriched source.

Rhenium and osmium are siderophile elements which are present at very low abundances in the crust. Rhenium undergoes radioactive decay to produce osmium. The ratio of non-radiogenic osmium to radiogenic osmium throughout time varies.

Rhenium prefers to enter sulfides more readily than osmium. Hence, during melting of the mantle, rhenium is stripped out, and prevents the osmium–osmium ratio from changing appreciably. This locks in an initial osmium ratio of the sample at the time of the melting event. Osmium–osmium initial ratios are used to determine the source characteristic and age of mantle melting events.

Helium-3 was trapped in the planet when it formed. Some ³He is being added by meteoric dust, primarily collecting on the bottom of oceans (although due to subduction, all oceanic tectonic plates are younger than continental plates). However, ³He will be degassed from oceanic sediment during subduction, so cosmogenic ³He is not affecting the concentration or noble gas ratios of the mantle.

Helium-3 is created by cosmic ray bombardment, and by lithium spallation reactions which generally occur in the crust. Lithium spallation is the process by which a high-energy neutron bombards a lithium atom, creating a ³He and a ⁴He ion. This requires significant lithium to adversely affect the ³He/⁴He ratio.

All degassed helium is lost to space eventually, due to the average speed of helium exceeding the escape velocity for the Earth. Thus, it is assumed the helium content and ratios of Earth's atmosphere have remained essentially stable.

It has been observed that ³He is present in volcano emissions and oceanic ridge samples. How ³He is stored in the planet is under investigation, but it is associated with the mantle and is used as a marker of material of deep origin.

Due to similarities in helium and carbon in magma chemistry, outgassing of helium requires the loss of volatile components (water, carbon dioxide) from the mantle, which happens at depths of less than 60 km. However, ³He is transported to the surface primarily trapped in the crystal lattice of minerals within fluid inclusions.

Helium-4 is created by radiogenic production (by decay of uranium/thorium-series elements). The continental crust has become enriched with those elements relative to the mantle and thus more He⁴ is produced in the crust than in the mantle.

The ratio (R) of ³He to ⁴He is often used to represent ³He content. R usually is given as a multiple of the present atmospheric ratio (Ra).

Common values for R/Ra:

• Old continental crust: less than 1
• mid-ocean ridge basalt (MORB): 7 to 9
• Spreading ridge rocks: 9.1 plus or minus 3.6
• Hotspot rocks: 5 to 42
• Ocean and terrestrial water: 1
• Sedimentary formation water: less than 1
• Thermal spring water: 3 to 11

³He/⁴He isotope chemistry is being used to date groundwaters, estimate groundwater flow rates, track water pollution, and provide insights into hydrothermal processes, igneous geology and ore genesis.

• (U-Th)/He dating of apatite as a thermal history tool
• USGS: Helium Discharge at Mammoth Mountain Fumarole (MMF)

Uranium is well mixed in the ocean, and its decay produces ²³¹Pa and ²³⁰Th at a constant activity ratio (0.093). The decay products are rapidly removed by adsorption on settling particles, but not at equal rates. ²³¹Pa has a residence equivalent to the residence time of deep water in the Atlantic basin (around 1000 yrs) but ²³⁰Th is removed more rapidly (centuries). Thermohaline circulation effectively exports ²³¹Pa from the Atlantic into the Southern Ocean, while most of the ²³⁰Th remains in Atlantic sediments. As a result, there is a relationship between ²³¹Pa/²³⁰Th in Atlantic sediments and the rate of overturning: faster overturning produces lower sediment ²³¹Pa/²³⁰Th ratio, while slower overturning increases this ratio. The combination of δ¹³C and ²³¹Pa/²³⁰Th can therefore provide a more complete insight into past circulation changes.

Tritium was released to the atmosphere during atmospheric testing of nuclear bombs. Radioactive decay of tritium produces the noble gas helium-3. Comparing the ratio of tritium to helium-3 (³H/³He) allows estimation of the age of recent ground waters. A small amount of Tritium is also produced naturally by cosmic ray spallation and spontaneous ternary fission in natural uranium and thorium, but due to the relatively short half-life of Tritium and the relatively small quantities (compared to those from humandmade sources) those sources of Tritium usually play only a secondary role in the analysis of groundwater.

• USGS Tritium/Helium-3 Dating
• Hydrologic Isotope Tracers - Helium

• Allègre C.J., 2008. Isotope Geology (Cambridge University Press).
• Dickin A.P., 2005. Radiogenic Isotope Geology (Cambridge University Press).
• Faure G., Mensing T.M. (2004), Isotopes: Principles and Applications (John Wiley & Sons).
• Hoefs J., 2004. Stable Isotope Geochemistry (Springer Verlag).
• Sharp Z., 2006. Principles of Stable Isotope Geochemistry (Prentice Hall).

• Environmental Isotopes  (University of Ottawa)
• Fundamentals of Isotope Geochemistry  (C. Kendall & E.A. Caldwell, chap.2 in Isotope Tracers in Catchment Hydrology [edited by C. Kendall & J.J. McDonnell], 1998)
• Stable Isotopes and Mineral Resource Investigations in the United States  (USGS)

• Burnard P. G., Farley K. A., Turner G. (1998). "Multiple fluid pulses in a Samoan harzburgite". Chemical Geology. 147 (1–2): 99–114. Bibcode:1998ChGeo.147...99B. doi:10.1016/s0009-2541(97)00175-7.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• Kirstein L., Timmerman M. (2000). "Evidence of the proto-Iceland lume in northwestern Ireland at 42Ma from helium isotopes". Journal of the Geological Society, London. 157 (5): 923–927. Bibcode:2000JGSoc.157..923K. doi:10.1144/jgs.157.5.923. S2CID 128600558.
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• Arne D., Bierlein F. P., Morgan J. W., Stein H. J. (2001). "Re-Os dating of sulfides associated with gold mineralisation in central Victoria, Australia". Economic Geology. 96 (6): 1455–1459. doi:10.2113/96.6.1455.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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