The technique of radiocarbon dating was developed by Willard Libby and his colleagues at the University of Chicago in 1949. Emilio Segrè asserted in his autobiography that Enrico Fermi suggested the concept to Libby in a seminar at Chicago that year. Libby estimated that the steady state radioactivity concentration of exchangeable carbon-14 would be about 14 disintegrations per minute (dpm) per gram. In 1960, he was awarded the Nobel Prize in chemistry for this work. He first demonstrated the accuracy of radiocarbon dating by accurately estimating the age of wood from an ancient Egyptian royal barge for which the age was known from historical documents.
Carbon has two stable, nonradioactive isotopes: carbon-12 (), and carbon-13 (). In addition, there are trace amounts of the unstable isotope carbon-14 () on Earth. Carbon-14 has a relatively short half-life of 5730 years, meaning that the amount of carbon-14 in a sample is halved over the course of 5730 years due to radioactive decay. Carbon-14 would have long ago vanished from Earth were it not for the unremitting cosmic ray flux interactions with the Earth's atmosphere, which create more of the isotope. The neutrons resulting from the cosmic ray interactions participate in the following nuclear reaction on the atoms of nitrogen molecules () in the atmosphere:
:
The highest rate of carbon-14 production takes place at altitudes of 9 to 15 km (30,000 to 50,000 ft), and at high geomagnetic latitudes, but the carbon-14 spreads evenly throughout the atmosphere and reacts with oxygen to form carbon dioxide. Carbon dioxide also permeates the oceans, dissolving in the water. For approximate analysis it is assumed that the cosmic ray flux is constant over long periods of time; thus carbon-14 is produced at a constant rate and the proportion of radioactive to non-radioactive carbon is constant: ca. 1 part per trillion (600 billion atoms/mole). In 1958 Hessel de Vries showed that the concentration of carbon-14 in the atmosphere varies with time and locality. For the most accurate work, these variations are compensated by means of calibration curves. When these curves are used, their accuracy and shape are the factors that determine the accuracy of the age obtained for a given sample. can also be produced at ground level at a rate of 1 x 10−4 g−1s−1, which is not considered significant enough to impact on dating without a known other source of neutrons.
Plants take up atmospheric carbon dioxide by photosynthesis, and are ingested by animals, so every living thing is constantly exchanging carbon-14 with its environment as long as it lives. Once it dies, however, this exchange stops, and the amount of carbon-14 gradually decreases through radioactive beta decay with a half-life of 5,730 ± 40 years. Carbon-14 is stored in different amounts in different reservoirs because there is a dynamic equilibrium between production and decay.
: Carbon-14 was discovered on February 27, 1940, by Martin Kamen and Sam Ruben at the University of California Radiation Laboratory at Berkeley.
For radiocarbon dating a once living organism, the initial ratio of atoms to the sum of all other carbon atoms at the point of the organism's death and hence the point when the decay started, is approximately the ratio in the atmosphere.
Two characteristic times can be defined: :* mean- or average-life: mean or average time each radiocarbon atom spends in a given sample until it decays. :* half-life: time lapsed for half the number of radiocarbon atoms in a given sample, to decay,
It can be shown that:
: = = radiocarbon mean- or average-life = 8033 years (Libby value)
: = = radiocarbon half-life = 5568 years (Libby value)
Notice that dates are customarily given in years BP which implies t(BP) = –t because the time arrow for dates runs in reverse direction from the time arrow for the corresponding ages. From these considerations and the above equation, it results:
For a raw radiocarbon date: : and for a raw radiocarbon age: :
After replacing values, the raw radiocarbon age becomes any of the following equivalent formulae:
using logs base e and the average life: :
and
using logs base 2 and the half-life: :
Wiggle matching uses the non-linear relationship between the age and calendar age to match the shape of a series of closely sequentially spaced dates with the calibration curve.
The sensitivity of the method has been greatly increased by the use of accelerator mass spectrometry (AMS). With this technique atoms can be detected and counted directly vs only detecting those atoms that decay during the time interval allotted for an analysis. AMS allows dating samples containing only a few milligrams of carbon.
Raw radiocarbon ages (i.e., those not calibrated) are usually reported in "years Before Present" (BP). This is the number of radiocarbon years before 1950, based on a nominal (and assumed constant – see "calibration" below) level of carbon-14 in the atmosphere equal to the 1950 level. These raw dates are also based on a slightly-off historic value for the radiocarbon half-life. Such value is used for consistency with earlier published dates (see "Radiocarbon half-life" below). See the section on computation for the basis of the calculations.
Radiocarbon dating laboratories generally report an uncertainty for each date. For example, 3000 ± 30 BP indicates a standard deviation of 30 radiocarbon years. Traditionally this included only the statistical counting uncertainty. However, some laboratories supplied an "error multiplier" that could be multiplied by the uncertainty to account for other sources of error in the measuring process. More recently, the laboratories try to quote the overall uncertainty, which is determined from control samples of known age and verified by international intercomparison exercises. In 2008, a typical uncertainty better than ±40 radiocarbon years can be expected for samples younger than 10,000 years. This, however, is only a small part of the uncertainty of the final age determination (see section Calibration below).
Samples older than the upper age-limit can't be dated because the small number of remaining intrinsic atoms will be obscured by background atoms introduced into the samples while they still resided in the environment, during sample preparation, or in the detection instrument. , the limiting age for a 1 milligram sample of graphite is about ten half-lives, approximately 60,000 years. This age is derived from that of the calibration blanks used in an analysis, whose content is assumed to be the result of contamination during processing (as a result of this, some facilities will not report an age greater than 60,000 years for any sample).
A variety of sample processing and instrument-based constraints have been postulated to explain the upper age-limit. To examine instrument-based background activities in the AMS instrument of the W. M. Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory of the University of California, a set of natural diamonds were dated. Natural diamond samples from different sources within rock formations with standard geological ages in excess of 100 Ma yielded apparent ages 64,920 ± 430 BP to 80,000 ± 1100 BP as reported in 2007.
Aside from these changes due to natural processes, the level has also been affected by human activities. From the beginning of the industrial revolution in the 18th century to the 1950s, the fractional level of decreased because of the admixture of large quantities of into the atmosphere, due to the excavated oil reserves and combustion production of fossil fuel. This decline is known as the Suess effect, and also affects the isotope. However, atmospheric was almost doubled during the 1950s and 1960s due to atmospheric atomic bomb tests.
The calibration curves can vary significantly from a straight line, so comparison of uncalibrated radiocarbon dates (e.g., plotting them on a graph or subtracting dates to give elapsed time) is likely to give misleading results. There are also significant plateaus in the curves, such as the one from 11,000 to 10,000 radiocarbon years BP, which is believed to be associated with changing ocean circulation during the Younger Dryas period. Over the historical period from 0 to 10,000 years BP, the average width of the uncertainty of calibrated dates was found to be 335 years, although in well-behaved regions of the calibration curve the width decreased to about 113 years while in ill-behaved regions it increased to a maximum of 801 years. Significantly, in the ill-behaved regions of the calibration curve, increasing the precision of the measurements does not have a significant effect on increasing the accuracy of the dates.
The 2004 version of the calibration curve extends back quite accurately to 26,000 years BP. Any errors in the calibration curve do not contribute more than ±16 years to the measurement error during the historic and late prehistoric periods (0–6,000 yrs BP) and no more than ±163 years over the entire 26,000 years of the curve, although its shape can reduce the accuracy as mentioned above.
In late 2009, the journal Radiocarbon announced agreement on the INTCAL09 standard, which extends a more accurate calibration curve to 50,000 years.
The chairman of the Cambridge conference, Harry Godwin, wrote to the scientific journal Nature, recommending that the Libby half-life continue to be used for the time being, as the Cambridge figure might itself be improved by future experiments. Laboratories today continue to use the Libby figure to avoid inconsistencies with earlier publications, although the Cambridge half-life is still the most accurate figure that is widely known and accepted. However, the inaccuracy of the Libby half-life is not relevant if calibration is applied: the mathematical term representing the half-life is canceled out as long as the same value is used throughout a calculation.
When is transferred from the atmosphere to the oceans, it initially shares the concentration of the atmosphere. However, turnaround times of in the ocean are similar to the half-life of (making also a dating tool for ocean water). Marine organisms feed on this "old" carbon, and thus their radiocarbon age reflects the time of uptake by the ocean rather than the time of death of the organism. This marine reservoir effect is partly handled by a special marine calibration curve, but local deviations of several hundred years exist.
Erosion and immersion of carbonate rocks (which are generally older than 80,000 years and so shouldn't contain measurable ) causes an increase in and in the exchange reservoir, which depends on local weather conditions and can vary the ratio of carbon that living organisms incorporate. This is believed negligible for the atmosphere and atmosphere-derived carbon since most erosion will flow into the sea. The atmospheric concentration may differ substantially from the concentration in local water reservoirs. Eroded from CaCO3 or organic deposits, old carbon may be assimilated easily and provide diluted carbon into trophic chains. So the method is less reliable for such materials as well as for samples derived from animals with such plants in their food chain.
Volcanic eruptions eject large amount of carbon into the air, causing an increase in and in the exchange reservoir and can vary the exchange ratio locally. This explains the often irregular dating achieved in volcanic areas.
The earth is not affected evenly by cosmic radiation, the magnitude of the radiation depends on land altitude and earth's magnetic field strength at any given location, causing minor variation in the local production. This is accounted for by having calibration curves for different locations of the globe. However this could not always be performed, as tree rings for calibration were only recoverable from certain locations in 1958. The rebuttals by Münnich et al. and by Barker both maintain that while variations of carbon-14 exist, they are about an order of magnitude smaller than those implied by Crowe's calculations.
These effects were first confirmed when samples of wood from around the world, which all had the same age (based on tree ring analysis), showed deviations from the dendrochronological age. Calibration techniques based on tree-ring samples have contributed to increased accuracy since 1962, when they were accurate to 700 years at worst.
Category:Radiometric dating Category:Radioactivity Category:Carbon Category:Isotopes of carbon Category:American inventions
bg:Радиовъглеродно датиране ca:Datació basada en el carboni-14 cs:Radiokarbonová metoda datování da:Kulstof 14-datering de:Radiokohlenstoffdatierung et:Radiosüsiniku meetod el:Ραδιοχρονολόγηση Άνθρακα 14 es:Datación por radiocarbono eo:Radiokarbona datado eu:Karbono-14 bidezko datazioa fr:Datation par le carbone 14 ko:방사성 탄소 연대 측정법 hi:कार्बन १४ डेटिंग hr:Datiranje ugljikom-14 id:Penanggalan radiokarbon is:C-14 aldursgreining it:Metodo del carbonio-14 he:תיארוך פחמן-14 hu:Radiokarbonos kormeghatározás mk:Радиојаглеродно датирање ml:കാര്ബണ് പഴക്കനിര്ണ്ണയം mr:कार्बन १४ किरणोत्सर्ग कालमापन पद्धती nl:C14-datering ne:कार्बन १४ डेटिंग ja:放射性炭素年代測定 no:Karbondatering nn:Radiokarbondatering pl:Datowanie radiowęglowe pt:Datação por radiocarbono ro:Datarea cu carbon ru:Радиоуглеродный анализ scn:Datazziuni cu lu radiucarboniu 14 simple:Radiocarbon dating sk:Uhlíková metóda C14 fi:Radiohiiliajoitus sv:C14-metoden ta:கதிரியக்கக்கரிமக் காலக்கணிப்பு tr:Radyokarbon tarihleme yöntemi uk:Радіовуглецеве датування zh:放射性碳定年法
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