Radiometric dating

Radiometric dating or radioactive dating is a technique used to date materials such as rocks or carbon, in which trace radioactive impurities were selectively incorporated when they formed. The method compares the abundance of a naturally occurring radioactive isotope within the material and the abundance of its decay products, which form at a known constant rate of decay.[1] The use of radiometric dating was first published in 1907 by Bertram Boltwood[2] and is now the principal source of information about the absolute age of rocks and other geological features, including the age of the Earth itself, and can be used to date a wide range of natural and man-made materials.

Together with stratigraphic principles, radiometric dating methods are used in geochronology to establish the geological time scale.[3] Among the best-known techniques are radiocarbon dating, potassium-argon dating and uranium-lead dating. By allowing the establishment of geological timescales, it provides a significant source of information about the ages of fossils and the deduced rates of evolutionary change. Radiometric dating is also used to date archaeological materials, including ancient artifacts.

Different methods of radiometric dating vary in the timescale over which they are accurate and the materials to which they can be applied.

Fundamentals of radiometric dating

Radioactive decay

Example of a radioactive decay chain from lead-212 (212Pb) to lead-208 (208Pb) . Each parent nuclide spontaneously decays into a daughter nuclide (the decay product) via an α decay or a β− decay. The final decay product, lead-208 (208Pb), is stable and can no longer undergo spontaneous radioactive decay.

All ordinary matter is made up of combinations of chemical elements, each with its own atomic number, indicating the number of protons in the atomic nucleus. Additionally, elements may exist in different isotopes, with each isotope of an element differing in the number of neutrons in the nucleus. A particular isotope of a particular element is called a nuclide. Some nuclides are inherently unstable. That is, at some point in time, an atom of such a nuclide will undergo radioactive decay and spontaneously transform into a different nuclide. This transformation may be accomplished in a number of different ways, including alpha decay (emission of alpha particles) and beta decay (electron emission, positron emission, or electron capture). Another possibility is spontaneous fission into two or more nuclides.

While the moment in time at which a particular nucleus decays is unpredictable, a collection of atoms of a radioactive nuclide decays exponentially at a rate described by a parameter known as the half-life, usually given in units of years when discussing dating techniques. After one half-life has elapsed, one half of the atoms of the nuclide in question will have decayed into a "daughter" nuclide or decay product. In many cases, the daughter nuclide itself is radioactive, resulting in a decay chain, eventually ending with the formation of a stable (nonradioactive) daughter nuclide; each step in such a chain is characterized by a distinct half-life. In these cases, usually the half-life of interest in radiometric dating is the longest one in the chain, which is the rate-limiting factor in the ultimate transformation of the radioactive nuclide into its stable daughter. Isotopic systems that have been exploited for radiometric dating have half-lives ranging from only about 10 years (e.g., tritium) to over 100 billion years (e.g., Samarium-147).

For most radioactive nuclides, the half-life depends solely on nuclear properties and is essentially a constant. It is not affected by external factors such as temperature, pressure, chemical environment, or presence of a magnetic or electric field.[4][5][6] The only exceptions are nuclides that decay by the process of electron capture, such as beryllium-7, strontium-85, and zirconium-89, whose decay rate may be affected by local electron density. For all other nuclides, the proportion of the original nuclide to its decay products changes in a predictable way as the original nuclide decays over time. This predictability allows the relative abundances of related nuclides to be used as a clock to measure the time from the incorporation of the original nuclides into a material to the present.

Accuracy of radiometric dating

Thermal ionization mass spectrometer used in radiometric dating.

The basic equation of radiometric dating requires that neither the parent nuclide nor the daughter product can enter or leave the material after its formation. The possible confounding effects of contamination of parent and daughter isotopes have to be considered, as do the effects of any loss or gain of such isotopes since the sample was created. It is therefore essential to have as much information as possible about the material being dated and to check for possible signs of alteration.[7] Precision is enhanced if measurements are taken on multiple samples from different locations of the rock body. Alternatively, if several different minerals can be dated from the same sample and are assumed to be formed by the same event and were in equilibrium with the reservoir when they formed, they should form an isochron. This can reduce the problem of contamination. In uranium-lead dating, the concordia diagram is used which also decreases the problem of nuclide loss. Finally, correlation between different isotopic dating methods may be required to confirm the age of a sample. For example, a study of the Amitsoq gneisses from western Greenland used five different radiometric dating methods to examine twelve samples and achieved agreement to within 30 Ma (mega-annum; million years) on an age of 3,640 Ma.[8]

Accurate radiometric dating generally requires that the parent has a long enough half-life that it will be present in significant amounts at the time of measurement (except as described below under "Dating with short-lived extinct radionuclides"), the half-life of the parent is accurately known, and enough of the daughter product is produced to be accurately measured and distinguished from the initial amount of the daughter present in the material. The procedures used to isolate and analyze the parent and daughter nuclides must be precise and accurate. This normally involves isotope ratio mass spectrometry.[9]

The precision of a dating method depends in part on the half-life of the radioactive isotope involved. For instance, carbon-14 has a half-life of 5,730 years. After an organism has been dead for 60,000 years, so little carbon-14 is left that accurate dating can not be established. On the other hand, the concentration of carbon-14 falls off so steeply that the age of relatively young remains can be determined precisely to within a few decades.[10]

Closure temperature

Main article: Closure temperature

If a material that selectively rejects the daughter nuclide is heated, any daughter nuclides that have been accumulated over time will be lost through diffusion, setting the isotopic "clock" to zero. The temperature at which this happens is known as the closure temperature or blocking temperature and is specific to a particular material and isotopic system. These temperatures are experimentally determined in the lab by artificially resetting sample minerals using a high-temperature furnace. As the mineral cools, the crystal structure begins to form and diffusion of isotopes is less easy. At a certain temperature, the crystal structure has formed sufficiently to prevent diffusion of isotopes. This temperature is what is known as closure temperature and represents the temperature below which the mineral is a closed system to isotopes. Thus an igneous or metamorphic rock or melt, which is slowly cooling, does not begin to exhibit measurable radioactive decay until it cools below the closure temperature. The age that can be calculated by radiometric dating is thus the time at which the rock or mineral cooled to closure temperature.[11][12] Dating of different minerals and/or isotope systems (with differing closure temperatures) within the same rock can therefore enable the tracking of the thermal history of the rock in question with time, and thus the history of metamorphic events may become known in detail. This field is known as thermochronology or thermochronometry.

The age equation

Sm/Nd isochron plotted of samples [13] from the Great Dyke, Zimbabwe. The age is calculated from the slope of the isochron (line) and the original composition from the intercept of the isochron with the y-axis.

The mathematical expression that relates radioactive decay to geologic time is[11][14]

D = D0 + N(t) (eλt − 1)

where

t is age of the sample,
D is number of atoms of the daughter isotope in the sample,
D0 is number of atoms of the daughter isotope in the original composition,
N is number of atoms of the parent isotope in the sample at time t (the present), given by N(t) = Noe-λt, and
λ is the decay constant of the parent isotope, equal to the inverse of the radioactive half-life of the parent isotope[15] times the natural logarithm of 2.

The equation is most conveniently expressed in terms of the measured quantity N(t) rather than the constant initial value No.

The above equation makes use of information on the composition of parent and daughter isotopes at the time the material being tested cooled below its closure temperature. This is well-established for most isotopic systems.[12][16] However, construction of an isochron does not require information on the original compositions, using merely the present ratios of the parent and daughter isotopes to a standard isotope. Plotting an isochron is used to solve the age equation graphically and calculate the age of the sample and the original composition.

Modern dating methods

Radiometric dating has been carried out since 1905 when it was invented by Ernest Rutherford as a method by which one might determine the age of the Earth. In the century since then the techniques have been greatly improved and expanded.[15] Dating can now be performed on samples as small as a nanogram using a mass spectrometer. The mass spectrometer was invented in the 1940s and began to be used in radiometric dating in the 1950s. It operates by generating a beam of ionized atoms from the sample under test. The ions then travel through a magnetic field, which diverts them into different sampling sensors, known as "Faraday cups", depending on their mass and level of ionization. On impact in the cups, the ions set up a very weak current that can be measured to determine the rate of impacts and the relative concentrations of different atoms in the beams.

Uranium-lead dating method

Main article: uranium-lead dating
A concordia diagram as used in uranium-lead dating, with data from the Pfunze Belt, Zimbabwe.[17] All the samples show loss of lead isotopes, but the intercept of the errorchron (straight line through the sample points) and the concordia (curve) shows the correct age of the rock.[12]

The uranium-lead radiometric dating scheme has been refined to the point that the error margin in dates of rocks can be as low as less than two million years in two-and-a-half billion years.[13][18] An error margin of 2–5% has been achieved on younger Mesozoic rocks.[19]

Uranium-lead dating is often performed on the mineral zircon (ZrSiO4), though it can be used on other materials, such as baddeleyite.[20] Zircon and baddeleyite incorporate uranium atoms into their crystalline structure as substitutes for zirconium, but strongly reject lead. Zircon has a very high closure temperature, is resistant to mechanical weathering and is very chemically inert. Zircon also forms multiple crystal layers during metamorphic events, which each may record an isotopic age of the event. In situ micro-beam analysis can be achieved via laser ICP-MS or SIMS techniques.[21]

One of its great advantages is that any sample provides two clocks, one based on uranium-235's decay to lead-207 with a half-life of about 700 million years, and one based on uranium-238's decay to lead-206 with a half-life of about 4.5 billion years, providing a built-in crosscheck that allows accurate determination of the age of the sample even if some of the lead has been lost. This can be seen in the concordia diagram, where the samples plot along an errorchron (straight line) which intersects the concordia curve at the age of the sample.

Samarium-neodymium dating method

This involves the alpha-decay of 147Sm to 143Nd with a half-life of 1.06 x 1011 years. Accuracy levels of within twenty million years in two-and-a-half billion years are achievable.[22]

Potassium-argon dating method

This involves electron capture or positron decay of potassium-40 to argon-40. Potassium-40 has a half-life of 1.3 billion years, and so this method is applicable to the oldest rocks. Radioactive potassium-40 is common in micas, feldspars, and hornblendes, though the closure temperature is fairly low in these materials, about 350 °C (mica) to 500 °C (hornblende).

Rubidium-strontium dating method

This is based on the beta decay of rubidium-87 to strontium-87, with a half-life of 50 billion years. This scheme is used to date old igneous and metamorphic rocks, and has also been used to date lunar samples. Closure temperatures are so high that they are not a concern. Rubidium-strontium dating is not as precise as the uranium-lead method, with errors of 30 to 50 million years for a 3-billion-year-old sample.

Uranium-thorium dating method

A relatively short-range dating technique is based on the decay of uranium-234 into thorium-230, a substance with a half-life of about 80,000 years. It is accompanied by a sister process, in which uranium-235 decays into protactinium-231, which has a half-life of 34,300 years.

While uranium is water-soluble, thorium and protactinium are not, and so they are selectively precipitated into ocean-floor sediments, from which their ratios are measured. The scheme has a range of several hundred thousand years. A related method is ionium-thorium dating, which measures the ratio of ionium (thorium-230) to thorium-232 in ocean sediment.

Radiocarbon dating method

Main article: Radiocarbon dating
Ale's Stones at Kåseberga, around ten kilometres south east of Ystad, Sweden were dated at 56 CE using the carbon-14 method on organic material found at the site.[23]

Carbon-14 is a radioactive isotope of carbon, with a half-life of 5,730 years,[24][25] which is very short compared with the above isotopes. In other radiometric dating methods, the heavy parent isotopes were produced by nucleosynthesis in supernovas, meaning that any parent isotope with a short half-life should be extinct by now. Carbon-14, though, is continuously created through collisions of neutrons generated by cosmic rays with nitrogen in the upper atmosphere and thus remains at a near-constant level on Earth. The carbon-14 ends up as a trace component in atmospheric carbon dioxide (CO2).

An organism acquires carbon during its lifetime. Plants acquire it through photosynthesis, and animals acquire it from consumption of plants and other animals. When an organism dies, it ceases to take in new carbon-14, and the existing isotope decays with a characteristic half-life (5730 years). The proportion of carbon-14 left when the remains of the organism are examined provides an indication of the time elapsed since its death. The carbon-14 dating limit lies around 58,000 to 62,000 years.[26]

The rate of creation of carbon-14 appears to be roughly constant, as cross-checks of carbon-14 dating with other dating methods show it gives consistent results. However, local eruptions of volcanoes or other events that give off large amounts of carbon dioxide can reduce local concentrations of carbon-14 and give inaccurate dates. The releases of carbon dioxide into the biosphere as a consequence of industrialization have also depressed the proportion of carbon-14 by a few percent; conversely, the amount of carbon-14 was increased by above-ground nuclear bomb tests that were conducted into the early 1960s. Also, an increase in the solar wind or the Earth's magnetic field above the current value would depress the amount of carbon-14 created in the atmosphere. These effects are addressed in the radiocarbon dating scale.[27]

Fission track dating method

Main article: fission track dating
Apatite crystals are widely used in fission track dating.

This involves inspection of a polished slice of a material to determine the density of "track" markings left in it by the spontaneous fission of uranium-238 impurities. The uranium content of the sample has to be known, but that can be determined by placing a plastic film over the polished slice of the material, and bombarding it with slow neutrons. This causes induced fission of 235U, as opposed to the spontaneous fission of 238U. The fission tracks produced by this process are recorded in the plastic film. The uranium content of the material can then be calculated from the number of tracks and the neutron flux.

This scheme has application over a wide range of geologic dates. For dates up to a few million years micas, tektites (glass fragments from volcanic eruptions), and meteorites are best used. Older materials can be dated using zircon, apatite, titanite, epidote and garnet which have a variable amount of uranium content.[28] Because the fission tracks are healed by temperatures over about 200 °C the technique has limitations as well as benefits. The technique has potential applications for detailing the thermal history of a deposit.

Chlorine-36 dating method

Large amounts of otherwise rare 36Cl were produced by irradiation of seawater during atmospheric detonations of nuclear weapons between 1952 and 1958. The residence time of 36Cl in the atmosphere is about 1 week. Thus, as an event marker of 1950s water in soil and ground water, 36Cl is also useful for dating waters less than 50 years before the present. 36Cl has seen use in other areas of the geological sciences, including dating ice and sediments.

Luminescence dating methods

Natural sources of radiation in the environment knock loose electrons in, say, a piece of pottery, and these electrons accumulate in defects in the material's crystal lattice structure. Heating or illuminating the object will release the captured electrons, producing a luminescence. When the sample is heated, at a certain temperature it will glow from the emission of electrons released from the defects, and this glow can be used to estimate the age of the sample to a threshold of approximately 15 percent of its true age. The date of a rock is reset when volcanic activity remelts it. The date of a piece of pottery is reset by the heat of the kiln. Typically temperatures greater than 400 degrees Celsius will reset the "clock". This is termed thermoluminescence.

Other methods

Other methods include:

Dating with short-lived extinct radionuclides

Absolute radiometric dating requires a measurable fraction of parent nucleus to remain in the sample rock. For rocks dating back to the beginning of the solar system, this requires extremely long-lived parent isotopes, making measurement of such rocks' exact ages imprecise. To be able to distinguish the relative ages of rocks from such old material, and to get a better time resolution than that available from long-lived isotopes, short-lived isotopes that are no longer present in the rock can be used.[29]

At the beginning of the solar system, there were several relatively short-lived radionuclides like 26Al, 60Fe, 53Mn, and 129I present within the solar nebula. These radionuclides—possibly produced by the explosion of a supernova—are extinct today, but their decay products can be detected in very old material, such as that which constitutes meteorites. By measuring the decay products of extinct radionuclides with a mass spectrometer and using isochronplots, it is possible to determine relative ages of different events in the early history of the solar system. Dating methods based on extinct radionuclides can also be calibrated with the U-Pb method to give absolute ages. Thus both the approximate age and a high time resolution can be obtained. Generally a shorter half-life leads to a higher time resolution at the expense of timescale.

The 129I – 129Xe chronometer

129I beta-decays to 129Xe with a half-life of 16 million years. The iodine-xenon chronometer[30] is an isochron technique. Samples are exposed to neutrons in a nuclear reactor. This converts the only stable isotope of iodine (127I) into 128Xe via neutron capture followed by beta decay (of 128I). After irradiation, samples are heated in a series of steps and the xenon isotopic signature of the gas evolved in each step is analysed. When a consistent 129Xe/128Xe ratio is observed across several consecutive temperature steps, it can be interpreted as corresponding to a time at which the sample stopped losing xenon.

Samples of a meteorite called Shallowater are usually included in the irradiation to monitor the conversion efficiency from 127I to 128Xe. The difference between the measured 129Xe/128Xe ratios of the sample and Shallowater then corresponds to the different ratios of 129I/127I when they each stopped losing xenon. This in turn corresponds to a difference in age of closure in the early solar system.

The 26Al – 26Mg chronometer

Another example of short-lived extinct radionuclide dating is the 26Al – 26Mg chronometer, which can be used to estimate the relative ages of chondrules. 26Al decays to 26Mg with a half-life of 720 000 years. The dating is simply a question of finding the deviation from the natural abundance of 26Mg (the product of 26Al decay) in comparison with the ratio of the stable isotopes 27Al/24Mg.

The excess of 26Mg (often designated 26Mg* ) is found by comparing the 26Mg/27Mg ratio to that of other Solar System materials.[31]

The 26Al – 26Mg chronometer gives an estimate of the time period for formation of primitive meteorites of only a few million years (1.4 million years for Chondrule formation).[32]

See also

References

  1. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "radioactive dating".
  2. ↑ Boltwood, Bertram (1907). "The Ultimate Disintegration Products of the Radio-active Elements. Part II. The disintegration products of uranium". American Journal of Science. 4 23: 77–88. doi:10.2475/ajs.s4-23.134.78.
  3. ↑ McRae, A. 1998. Radiometric Dating and the Geological Time Scale: Circular Reasoning or Reliable Tools? Radiometric Dating and the Geological Time Scale TalkOrigins Archive
  4. ↑ Emery, G T (1972). "Perturbation of Nuclear Decay Rates". Annual Review of Nuclear Science 22 (1): 165–202. Bibcode:1972ARNPS..22..165E. doi:10.1146/annurev.ns.22.120172.001121.
  5. ↑ Shlyakhter, A. I. (1976). "Direct test of the constancy of fundamental nuclear constants". Nature 264 (5584): 340. Bibcode:1976Natur.264..340S. doi:10.1038/264340a0.
  6. ↑ Johnson, B. 1993. How to Change Nuclear Decay Rates Usenet Physics FAQ
  7. ↑ Stewart, K,, Turner, S, Kelley, S, Hawkesworh, C Kristein, L and Manotvani, M (1996). "3-D, 40Ar---39Ar geochronology in the Paraná continental flood basalt province". Earth and Planetary Science Letters 143 (1-4): 95–109. Bibcode:1996E&PSL.143...95S. doi:10.1016/0012-821X(96)00132-X.
  8. ↑ Dalrymple, G. B. (1991). The Age of the Earth. Stanford, California: Stanford University Press. ISBN 0-8047-1569-6.
  9. ↑ Dickin, Alan P. (2005). Radiogenic isotope geology. Cambridge: Cambridge University Press. ISBN 0-521-53017-2.
  10. ↑ Reimer Paula J, et al. (2004). "INTCAL04 Terrestrial Radiocarbon Age Calibration, 0–26 Cal Kyr BP" (PDF). Radiocarbon 46 (3): 1029–1058.
  11. 1 2 Faure, Gunter (1998). Principles and applications of geochemistry: a comprehensive textbook for geology students (2nd ed.). Englewood Cliffs, New Jersey: Prentice Hall. ISBN 0-02-336450-5. OCLC 37783103.
  12. 1 2 3 Rollinson, Hugh R. (1993). Using geochemical data: evaluation, presentation, interpretation. Harlow: Longman. ISBN 0-582-06701-4. OCLC 27937350.
  13. 1 2 Oberthür, T, Davis, DW, Blenkinsop, TG, Hoehndorf, A (2002). "Precise U–Pb mineral ages, Rb–Sr and Sm–Nd systematics for the Great Dyke, Zimbabwe—constraints on late Archean events in the Zimbabwe craton and Limpopo belt". Precambrian Research 113 (3-4): 293–306. doi:10.1016/S0301-9268(01)00215-7.
  14. ↑ White, W. M. (2003). "Basics of Radioactive Isotope Geochemistry" (PDF). Cornell University.
  15. 1 2 "Geologic Time: Radiometric Time Scale". United States Geological Survey. 16 June 2001.
  16. ↑ Stacey, J. S.; J. D. Kramers (June 1975). "Approximation of terrestrial lead isotope evolution by a two-stage model". Earth and Planetary Science Letters 26 (2): 207–221. Bibcode:1975E&PSL..26..207S. doi:10.1016/0012-821X(75)90088-6.
  17. ↑ Vinyu, M. L.; R. E. Hanson; M. W. Martin; S. A. Bowring; H. A. Jelsma; P. H. G. M. Dirks (2001). "U-Pb zircon ages from a craton-margin archaean orogenic belt in northern Zimbabwe". Journal of African Earth Sciences 32 (1): 103–114. Bibcode:2001JAfES..32..103V. doi:10.1016/S0899-5362(01)90021-1.
  18. ↑ Manyeruke, Tawanda D.; Thomas G. Blenkinsop; Peter Buchholz; David Love; Thomas Oberthür; Ulrich K. Vetter; Donald W. Davis (2004). "The age and petrology of the Chimbadzi Hill Intrusion, NW Zimbabwe: first evidence for early Paleoproterozoic magmatism in Zimbabwe". Journal of African Earth Sciences 40 (5): 281–292. Bibcode:2004JAfES..40..281M. doi:10.1016/j.jafrearsci.2004.12.003.
  19. ↑ Li, Xian-hua; Xi-rong Liang, Min Sun, Hong Guan and J. G. Malpas (2001). "Precise 206Pb/238U age determination on zircons by laser ablation microprobe-inductively coupled plasma-mass spectrometry using continuous linear ablation". Chemical Geology 175 (3-4): 209–219. doi:10.1016/S0009-2541(00)00394-6. Cite uses deprecated parameter |coauthors= (help)
  20. ↑ Wingate, M.T.D. (2001). "SHRIMP baddeleyite and zircon ages for an Umkondo dolerite sill, Nyanga Mountains, Eastern Zimbabwe". South African Journal of Geology 104 (1): 13–22. doi:10.2113/104.1.13.
  21. ↑ Ireland, Trevor (December 1999). "Isotope Geochemistry: New Tools for Isotopic Analysis". Science 286 (5448): 2289–2290. doi:10.1126/science.286.5448.2289.
  22. ↑ Mukasa, S. B.; A. H. Wilson; R. W. Carlson (December 1998). "A multielement geochronologic study of the Great Dyke, Zimbabwe: significance of the robust and reset ages". Earth and Planetary Science Letters 164 (1–2): 353–369. Bibcode:1998E&PSL.164..353M. doi:10.1016/S0012-821X(98)00228-3.
  23. ↑ "Ales stenar". The Swedish National Heritage Board. 11 October 2006. Retrieved 9 March 2009.
  24. ↑ Clark, R. M. (1975). "A calibration curve for radiocarbon dates". Antiquity 49: 251–266.
  25. ↑ Vasiliev, S. S.; V. A. Dergachev (2002). "The ~2400-year cycle in atmospheric radiocarbon concentration: Bispectrum of 14C data over the last 8000 years" (PDF). Annales Geophysicae 20 (1): 115–120. Bibcode:2002AnGeo..20..115V. doi:10.5194/angeo-20-115-2002.
  26. ↑ Plastino, Wolfango; Lauri Kaihola; Paolo Bartolomei; Francesco Bella (2001). "Cosmic background reduction in the radiocarbon measurement by scintillation spectrometry at the underground laboratory of Gran Sasso" (PDF). Radiocarbon 43 (2A): 157–161.
  27. ↑ Sources for this paragraph can be found at Radiocarbon dating#Calibration
  28. ↑ Jacobs, J.; R. J. Thomas (August 2001). "A titanite fission track profile across the southeastern Archæan Kaapvaal Craton and the Mesoproterozoic Natal Metamorphic Province, South Africa: evidence for differential cryptic Meso- to Neoproterozoic tectonism". Journal of African Earth Sciences 33 (2): 323–333. Bibcode:2001JAfES..33..323J. doi:10.1016/S0899-5362(01)80066-X.
  29. ↑ Imke de Pater and Jack J. Lissauer: Planetary Sciences, page 321. Cambridge University Press, 2001. ISBN 0-521-48219-4
  30. ↑ Gilmour, J. D.; O. V Pravdivtseva; A. Busfield; C. M. Hohenberg (2006). "The I-Xe Chronometer and the Early Solar System". Meteoritics and Planetary Science 41: 19–31. Bibcode:2006M&PS...41...19G. doi:10.1111/j.1945-5100.2006.tb00190.x. Retrieved 2013-01-21.
  31. ↑ Alexander N. Krot(2002) Dating the Earliest Solids in our Solar System, Hawai'i Institute of Geophysics and Planetology http://www.psrd.hawaii.edu/Sept02/isotopicAges.html.
  32. ↑ Imke de Pater and Jack J. Lissauer: Planetary Sciences, page 322. Cambridge University Press, 2001. ISBN 0-521-48219-4
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