(Redirected from Isotope geology)'Isotope geochemistry' is an aspect of
geology based upon study of the relative and absolute concentrations of the
elements and their
isotopes in the
Earth. Broadly, the field is divided into two branches:
stable and
radiogenic isotope geochemistry.
Lead-lead isotope geochemistry
Lead has four stable
isotopes -
204Pb,
206Pb,
207Pb,
208Pb and one common radiogenic isotope
202Pb with a
half-life of ~53,000 years.
Lead is created in the Earth via decay of
transuranic 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
Main articles: Samarium-neodymium dating
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 1.06x10
11 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-osmium
Rhenium and
osmium are chalcophile 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.
Noble gas isotopes
Helium-3
Helium-3 was trapped in the planet when it was created. 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 He
4 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)
Ground water isotopes
Tritium/helium-3
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.
★
USGS Tritium/Helium-3 Dating
★
Hydrologic Isotope Tracers - Helium
See also
★
Radiometric dating
★
Isotopic signature
★
Cosmogenic isotopes
★
Geochemistry
General online stable isotope references
★
USGS: Stable Isotopes and Mineral Resource Investigations in the United States
★
USGS: Fundamentals of Stable Isotope Geochemistry
★
Environmental Isotopes
★
Fundamentals of Isotope Geochemistry
References
3He/
4He
Burnard P.G., Farley K.A., & Turner G., 1998. ''Multiple fluid pulses in a Samoan
harzburgite.'' Chemical Geology, 147, pp. 99-114.
Kirstein L. & Timmerman M., 2000. ''Evidence of the proto-Iceland lume in northwestern Ireland at 42Ma from helium isotopes.'' Journal of the Geophysical Society, London. Vol 157, pp. 923-927.
Porcelli D. & Halliday A.N., 2001. ''The core as a possible source of mantle helium.'' Earth and Planetary Science Letters, 192, pp. 45-56.
Re-Os
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, pp. 1455-1459.
Martin C., 1991. ''Osmium isotopic characteristics of mantle-derived rocks.'' Geochimica et Cosmochimica Acta, 55, pp. 1421-1434.