Isochron dating

Last updated
An isochron plot of the radiogenic daughter isotope (D*) against the parent isotope (P), all normalized to a stable isotope of the daughter element (Dref). It demonstrates the isotopic evolution as the sample ages from t0 to t1 to t2. Isochron.jpg
An isochron plot of the radiogenic daughter isotope (D*) against the parent isotope (P), all normalized to a stable isotope of the daughter element (Dref). It demonstrates the isotopic evolution as the sample ages from t0 to t1 to t2.

Isochron dating is a common technique of radiometric dating and is applied to date certain events, such as crystallization, metamorphism, shock events, and differentiation of precursor melts, in the history of rocks. Isochron dating can be further separated into mineral isochron dating and whole rock isochron dating; both techniques are applied frequently to date terrestrial and extraterrestrial rocks (meteorites and Moon rocks). The advantage of isochron dating as compared to simple radiometric dating techniques is that no assumptions are needed about the initial amount of the daughter nuclide in the radioactive decay sequence. Indeed, the initial amount of the daughter product can be determined using isochron dating. This technique can be applied if the daughter element has at least one stable isotope other than the daughter isotope into which the parent nuclide decays. [1] [2] [3]

Contents

Basis for method

All forms of isochron dating assume that the source of the rock or rocks contained unknown amounts of both radiogenic and non-radiogenic isotopes of the daughter element, along with some amount of the parent nuclide. Thus, at the moment of crystallization, the ratio of the concentration of the radiogenic isotope of the daughter element to that of the non-radiogenic isotope is some value independent of the concentration of the parent. As time goes on, some amount of the parent decays into the radiogenic isotope of the daughter, increasing the ratio of the concentration of the radiogenic isotope to that of the non-radiogenic isotope of the daughter element. The greater the initial concentration of the parent, the greater the concentration of the radiogenic daughter isotope will be at some particular time. Thus, the ratio of the radiogenic to non-radiogenic isotopes of the daughter element will become larger with time, while the ratio of parent to daughter will become smaller. For rocks that start out with a small concentration of the parent, the radiogenic/non-radiogenic ratio of the daughter element will not change as quickly as it will with rocks that start out with a large concentration of the parent.

Assumptions

An isochron diagram will only give a valid age if all samples are cogenetic, which means they have the same initial isotopic composition (that is, the rocks are from the same unit, the minerals are from the same rock, etc.), all samples have the same initial isotopic composition (at t0), and the system has remained closed.

Isochron plots

The mathematical expression from which the isochron is derived is [4] [5]

where

t is age of the sample,
D* is number of atoms of the radiogenic daughter isotope in the sample,
D0 is number of atoms of the daughter isotope in the original or initial composition,
n is number of atoms of the parent isotope in the sample at the present,
λ is the decay constant of the parent isotope, equal to the inverse of the radioactive half-life of the parent isotope [6] times the natural logarithm of 2, and
(eλt-1) is the slope of the isochron which defines the age of the system.


Because the isotopes are measured by mass spectrometry, ratios are used instead of absolute concentrations since mass spectrometers usually measure the former rather than the latter. (See the section on isotope ratio mass spectrometry.) As such, isochrons are typically defined by the following equation, which normalizes the concentration of parent and radiogenic daughter isotopes to the concentration of a non-radiogenic isotope of the daughter element that is assumed to be constant:

where

is the concentration of the non-radiogenic isotope of the daughter element (assumed constant),
is the present concentration of the radiogenic daughter isotope,
is the initial concentration of the radiogenic daughter isotope, and
is the present concentration of the parent isotope that has decayed over time .


To perform dating, a rock is crushed to a fine powder, and minerals are separated by various physical and magnetic means. Each mineral has different ratios between parent and daughter concentrations. For each mineral, the ratios are related by the following equation:

         (1)

where

is the initial concentration of the parent isotope, and
is the total amount of the parent isotope which has decayed by time .


The proof of (1) amounts to simple algebraic manipulation. It is useful in this form because it exhibits the relationship between quantities that actually exist at present. To wit, , and respectively correspond to the concentrations of parent, daughter and non-radiogenic isotopes found in the rock at the time of measurement.

The ratios or (relative concentration of present daughter and non-radiogenic isotopes) and or (relative concentration of present parent and non-radiogenic isotope) are measured by mass spectrometry and plotted against each other in a three-isotope plot known as an isochron plot.

If all data points lie on a straight line, this line is called an isochron. The better the fit of the data points to a line, the more reliable the resulting age estimate. Since the ratio of the daughter and non-radiogenic isotopes is proportional to the ratio of the parent and non-radiogenic isotopes, the slope of the isochron gets steeper with time. The change in slope from initial conditions—assuming an initial isochron slope of zero (a horizontal isochron) at the point of intersection (intercept) of the isochron with the y-axis—to the current computed slope gives the age of the rock. The slope of the isochron, or , represents the ratio of daughter to parent as used in standard radiometric dating and can be derived to calculate the age of the sample at time t. The y-intercept of the isochron line yields the initial radiogenic daughter ratio, .

Whole rock isochron dating uses the same ideas but instead of different minerals obtained from one rock uses different types of rocks that are derived from a common reservoir; e.g. the same precursor melt. It is possible to date the differentiation of the precursor melt which then cooled and crystallized into the different types of rocks.

One of the best known isotopic systems for isochron dating is the rubidium–strontium system. Other systems that are used for isochron dating include samarium–neodymium, and uranium–lead. Some isotopic systems based on short-living extinct radionuclides such as 53Mn, 26Al, 129I, 60Fe and others are used for isochron dating of events in the early history of the Solar System. However, methods using extinct radionuclides give only relative ages and have to be calibrated with radiometric dating techniques based on long-living radionuclides like Pb-Pb dating to give absolute ages.

Application

Isochron dating is useful in the determination of the age of igneous rocks, which have their initial origin in the cooling of liquid magma. It is also useful to determine the time of metamorphism, shock events (such as the consequence of an asteroid impact) and other events depending on the behaviour of the particular isotopic systems under such events. It can be used to determine the age of grains in sedimentary rocks and understand their origin by a method known as a provenance study.

See also

Related Research Articles

In a chemical reaction, chemical equilibrium is the state in which both the reactants and products are present in concentrations which have no further tendency to change with time, so that there is no observable change in the properties of the system. This state results when the forward reaction proceeds at the same rate as the reverse reaction. The reaction rates of the forward and backward reactions are generally not zero, but they are equal. Thus, there are no net changes in the concentrations of the reactants and products. Such a state is known as dynamic equilibrium.

Power is the amount of energy transferred or converted per unit time. In the International System of Units, the unit of power is the watt, equal to one joule per second. Power is a scalar quantity.

Radiometric dating, radioactive dating or radioisotope dating is a technique which is used to date materials such as rocks or carbon, in which trace radioactive impurities were selectively incorporated when they were formed. The method compares the abundance of a naturally occurring radioactive isotope within the material to the abundance of its decay products, which form at a known constant rate of decay. The use of radiometric dating was first published in 1907 by Bertram Boltwood and is now the principal source of information about the absolute age of rocks and other geological features, including the age of fossilized life forms or the age of Earth itself, and can also be used to date a wide range of natural and man-made materials.

The rubidium–strontium dating method (Rb–Sr) is a radiometric dating technique, used by scientists to determine the age of rocks and minerals from their content of specific isotopes of rubidium (87Rb) and strontium. One of the two naturally occurring isotopes of rubidium, 87Rb, decays to 87Sr with a half-life of 49.23 billion years. The radiogenic daughter, 87Sr, produced in this decay process is the only one of the four naturally occurring strontium isotopes that was not produced exclusively by stellar nucleosynthesis predating the formation of the Solar System. Over time, decay of 87Rb increases the amount of radiogenic 87Sr while the amount of other Sr isotopes remains unchanged.

In fluid mechanics, the Grashof number is a dimensionless number which approximates the ratio of the buoyancy to viscous forces acting on a fluid. It frequently arises in the study of situations involving natural convection and is analogous to the Reynolds number.

In fluid mechanics, the Rayleigh number (Ra, after Lord Rayleigh) for a fluid is a dimensionless number associated with buoyancy-driven flow, also known as free (or natural) convection. It characterises the fluid's flow regime: a value in a certain lower range denotes laminar flow; a value in a higher range, turbulent flow. Below a certain critical value, there is no fluid motion and heat transfer is by conduction rather than convection. For most engineering purposes, the Rayleigh number is large, somewhere around 106 to 108.

In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities of the chemical species undergoing reduction and oxidation respectively. It was named after Walther Nernst, a German physical chemist who formulated the equation.

<span class="mw-page-title-main">Helmholtz free energy</span> Thermodynamic potential

In thermodynamics, the Helmholtz free energy is a thermodynamic potential that measures the useful work obtainable from a closed thermodynamic system at a constant temperature (isothermal). The change in the Helmholtz energy during a process is equal to the maximum amount of work that the system can perform in a thermodynamic process in which temperature is held constant. At constant temperature, the Helmholtz free energy is minimized at equilibrium.

The equilibrium constant of a chemical reaction is the value of its reaction quotient at chemical equilibrium, a state approached by a dynamic chemical system after sufficient time has elapsed at which its composition has no measurable tendency towards further change. For a given set of reaction conditions, the equilibrium constant is independent of the initial analytical concentrations of the reactant and product species in the mixture. Thus, given the initial composition of a system, known equilibrium constant values can be used to determine the composition of the system at equilibrium. However, reaction parameters like temperature, solvent, and ionic strength may all influence the value of the equilibrium constant.

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.

Uranium–lead dating, abbreviated U–Pb dating, is one of the oldest and most refined of the radiometric dating schemes. It can be used to date rocks that formed and crystallised from about 1 million years to over 4.5 billion years ago with routine precisions in the 0.1–1 percent range.

Samarium–neodymium dating is a radiometric dating method useful for determining the ages of rocks and meteorites, based on the alpha decay of the long-lived samarium isotope to the stable radiogenic neodymium isotope. Neodymium isotope ratios together with samarium–neodymium ratios are used to provide information on the age and source of igneous melts. It is sometimes assumed that at the moment when crustal material is formed from the mantle the neodymium isotope ratio depends only on the time when this event occurred, but thereafter it evolves in a way that depends on the new ratio of samarium to neodymium in the crustal material, which will be different from the ratio in the mantle material. Samarium–neodymium dating allows the determination of when the crustal material was formed.

Lead–lead dating is a method for dating geological samples, normally based on 'whole-rock' samples of material such as granite. For most dating requirements it has been superseded by uranium–lead dating, but in certain specialized situations it is more important than U–Pb dating.

Rhenium–osmium dating is a form of radiometric dating based on the beta decay of the isotope 187Re to 187Os. This normally occurs with a half-life of 41.6 × 109 y, but studies using fully ionised 187Re atoms have found that this can decrease to only 33 y. Both rhenium and osmium are strongly siderophilic (iron loving), while Re is also chalcophilic (sulfur loving) making it useful in dating sulfide ores such as gold and Cu–Ni deposits.

Samarium-147 (147Sm or Sm-147) is an isotope of samarium, making up 15% of natural samarium. It is an extremely long-lived radioisotope, with a half-life of 1.06×1011 years, although measurements have ranged from 1.05×1011 to 1.17×1011 years. It is mainly used in radiometric dating.

Equilibrium chemistry is concerned with systems in chemical equilibrium. The unifying principle is that the free energy of a system at equilibrium is the minimum possible, so that the slope of the free energy with respect to the reaction coordinate is zero. This principle, applied to mixtures at equilibrium provides a definition of an equilibrium constant. Applications include acid–base, host–guest, metal–complex, solubility, partition, chromatography and redox equilibria.

Thermal ionization, also known as surface ionization or contact ionization, is a physical process whereby the atoms are desorbed from a hot surface, and in the process are ionized.

Potassium–calcium dating, abbreviated K–Ca dating, is a radiometric dating method used in geochronology. It is based upon measuring the ratio of a parent isotope of potassium to a daughter isotope of calcium. This form of radioactive decay is accomplished through beta decay.

<span class="mw-page-title-main">Lutetium–hafnium dating</span> Gochronological dating method utilizing the radioactive decay system of lutetium–176

Lutetium–hafnium dating is a geochronological dating method utilizing the radioactive decay system of lutetium–176 to hafnium–176. With a commonly accepted half-life of 37.1 billion years, the long-living Lu–Hf decay pair survives through geological time scales, thus is useful in geological studies. Due to chemical properties of the two elements, namely their valences and ionic radii, Lu is usually found in trace amount in rare-earth element loving minerals, such as garnet and phosphates, while Hf is usually found in trace amount in zirconium-rich minerals, such as zircon, baddeleyite and zirkelite.

In combustion, Zeldovich–Liñán model is a two-step reaction model for the combustion processes, named after Yakov Borisovich Zeldovich and Amable Liñán. The model includes a chain-branching and a chain-breaking reaction. The model was first introduced by Zeldovich in 1948 and later analysed by Liñán using activation energy asymptotics in 1971. The mechanism with a quadratic or second-order recombination that were originally studied reads as

References

  1. Albarède, Francis (2009). "4.3 The isochron method". Geochemistry: An Introduction. Cambridge University Press. ISBN   9781107268883.
  2. Young, Matt; Strode, Paul K. (2009). Why evolution works (and creationism fails). New Brunswick, N.J.: Rutgers University Press. pp. 151–153. ISBN   9780813548647.
  3. Prothero, Donald R.; Schwab, Fred (2004). Sedimentary geology : an introduction to sedimentary rocks and stratigraphy (2nd ed.). New York: Freeman. ISBN   9780716739050.
  4. Faure, Gunter (1998). Principles and applications of geochemistry: a comprehensive textbook for geology students (2nd ed.). Englewood Cliffs, New Jersey: Prentice Hall. ISBN   978-0-02-336450-1. OCLC   37783103.[ page needed ]
  5. White, W. M. (2003). "Basics of Radioactive Isotope Geochemistry" (PDF). Cornell University.
  6. "Geologic Time: Radiometric Time Scale". United States Geological Survey. 16 June 2001.