The bomb pulse is the sudden increase of carbon-14 (14C) in the Earth's atmosphere due to the hundreds of above-ground nuclear bombs tests that started in 1945 and intensified after 1950 until 1963, when the Limited Test Ban Treaty was signed by the United States, the Soviet Union and the United Kingdom. [2] These hundreds of blasts were followed by a doubling of the relative concentration of 14C in the atmosphere. [3]
The reason for the term “relative concentration”, is because the measurements of 14C levels by mass spectrometers are most accurately made by comparison to another carbon isotope, often the common isotope 12C. Isotope abundance ratios are not only more easily measured, they are what 14C carbon daters want, since it is the fraction of carbon in a sample that is 14C, not the absolute concentration, that is of interest in dating measurements. The figure shows how the fraction of carbon in the atmosphere that is 14C, of order only a part per trillion, has changed over the past several decades following the bomb tests. Because 12C concentration has increased by about 30% over the past fifty years, the fact that “pMC”, measuring the isotope ratio, has returned (almost) to its 1955 value, means that 14C concentration in the atmosphere remains some 30% higher than it once was. Carbon-14, the radioisotope of carbon, is naturally developed in trace amounts in the atmosphere and it can be detected in all living organisms. Carbon of all types is continually used to form the molecules of the cells of organisms. Doubling of the concentration of 14C in the atmosphere is reflected in the tissues and cells of all organisms that lived around the period of nuclear testing. This property has many applications in the fields of biology and forensics.
The radioisotope carbon-14 is constantly formed from nitrogen-14 (14N) in the higher atmosphere by incoming cosmic rays which generate neutrons. These neutrons collide with 14N to produce 14C which then combines with oxygen to form 14CO2. This radioactive CO2 spreads through the lower atmosphere and the oceans where it is absorbed by the plants and the animals that eat the plants. The radioisotope 14C thus becomes part of the biosphere so that all living organisms contain a certain amount of 14C. Nuclear testing caused a rapid increase in atmospheric 14C (see figure), since the explosion of an atomic bomb also creates neutrons which collide again with 14N and produce 14C. Since the ban on nuclear testing in 1963, atmospheric 14C relative concentration is slowly decreasing at a pace of 4% annually. This continuous decrease permits scientists to determine among others the age of deceased people and allows them to study cell activity in tissues. By measuring the amount of 14C in a population of cells and comparing that to the amount of 14C in the atmosphere during or after the bomb pulse, scientists can estimate when the cells were created and how often they've turned over since then. [3]
Radiocarbon dating has been used since 1946 to determine the age of organic material as old as 50,000 years. As the organism dies, the exchange of 14C with the environment ceases and the incorporated 14C decays. Given the steady decay of radioisotopes (the half-life of 14C is about 5,730 years), the relative amount of 14C left in the dead organism can be used to calculate how long ago it died. Bomb pulse dating should be considered a special form of carbon dating. As discussed above and in the Radiolab episode, Elements (section 'Carbon'), [4] in bomb pulse dating the slow absorption of atmospheric 14C by the biosphere, can be considered as a chronometer. Starting from the pulse around the years 1963 (see figure), atmospheric radiocarbon relative abundance decreased by about 4% a year. So in bomb pulse dating it is the relative amount of 14C in the atmosphere that is decreasing and not the amount of 14C in a dead organisms, as is the case in classical radiocarbon dating. This decrease in atmospheric 14C can be measured in cells and tissues and has permitted scientists to determine the age of individual cells and of deceased people. [5] [6] [7] These applications are very similar to the experiments conducted with pulse-chase analysis in which cellular processes are examined over time by exposing the cells to a labeled compound (pulse) and then to the same compound in an unlabeled form (chase). Radioactivity is a commonly used label in these experiments. An important difference between pulse-chase analysis and bomb-pulse dating is the absence of the chase in the latter.
Around the year 2030 the bomb pulse will die out. Every organism born after this will not bear detectable bomb pulse traces and their cells cannot be dated in this way. Radioactive pulses cannot ethically be administered to people just to study the turnover of their cells so the bomb pulse results may be considered as a useful side effect of nuclear testing. [4]
The fact that cells and tissues reflect the doubling of 14C in the atmosphere during and after nuclear testing, has been of great use for several biological studies, for forensics and even for the determination of the year in which certain wine was produced. [8]
Biological studies carried out by Kirsty Spalding demonstrated that neuronal cells are essentially static and do not regenerate during life. [9] She also showed that the number of fat cells is set during childhood and adolescence. Considering the amount of 14C present in DNA she could establish that 10% of fat cells are renewed annually. [10] The radiocarbon bomb pulse has been used to validate otolith annuli (ages scored from otolith sections) across several fish species including the freshwater drum, [11] lake sturgeon, [12] pallid sturgeon, [13] bigmouth buffalo, [14] arctic salmonids, [15] Pristipomoides filamentosus [16] , several reef fishes, [17] among numerous other validated freshwater and marine species. The precision for bomb radiocarbon age validation is typically within +/- 2 years because the rise period (1956-1960) is so steep. [11] [14] [15] The bomb pulse has also been used to estimate (not validate) the age of Greenland sharks by measuring the incorporation of 14C in the eye lens during development. After having determined the age and measured the length of sharks born around the bomb pulse, it was possible to create a mathematical model in which length and age of the sharks were correlated in order to deduce the age of the larger sharks. The study showed that the Greenland shark, with an age of 392 +/- 120 years, is the oldest known vertebrate. [18]
At the moment of death, carbon uptake is ended. Considering that tissue that contained the bomb pulse 14C was rapidly diminishing with a rate of 4% per year, it has been possible to establish the time of death of two women in a court case by examining tissues with a rapid turnover. [5] Another important application has been the identification of victims of the Southeast Asian tsunami 2004 by examining their teeth. [6]
The perturbation in atmospheric 14C from the bomb testing was an opportunity to validate atmospheric transport models, and to study the movement of carbon between the atmosphere and oceanic or terrestrial sinks. [19]
Atmospheric bomb 14C has been used to validate tree ring ages and to date recent trees that have no annual growth rings. [20] It can also be used to obtain the growth rate of tropical trees and palms that have no visible annual rings. [21]
Radiocarbon dating is a method for determining the age of an object containing organic material by using the properties of radiocarbon, a radioactive isotope of carbon.
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.
A radionuclide (radioactive nuclide, radioisotope or radioactive isotope) is a nuclide that has excess numbers of either neutrons or protons, giving it excess nuclear energy, and making it unstable. This excess energy can be used in one of three ways: emitted from the nucleus as gamma radiation; transferred to one of its electrons to release it as a conversion electron; or used to create and emit a new particle (alpha particle or beta particle) from the nucleus. During those processes, the radionuclide is said to undergo radioactive decay. These emissions are considered ionizing radiation because they are energetic enough to liberate an electron from another atom. The radioactive decay can produce a stable nuclide or will sometimes produce a new unstable radionuclide which may undergo further decay. Radioactive decay is a random process at the level of single atoms: it is impossible to predict when one particular atom will decay. However, for a collection of atoms of a single nuclide the decay rate, and thus the half-life (t1/2) for that collection, can be calculated from their measured decay constants. The range of the half-lives of radioactive atoms has no known limits and spans a time range of over 55 orders of magnitude.
Carbon-14, C-14, 14C or radiocarbon, is a radioactive isotope of carbon with an atomic nucleus containing 6 protons and 8 neutrons. Its presence in organic matter is the basis of the radiocarbon dating method pioneered by Willard Libby and colleagues (1949) to date archaeological, geological and hydrogeological samples. Carbon-14 was discovered on February 27, 1940, by Martin Kamen and Sam Ruben at the University of California Radiation Laboratory in Berkeley, California. Its existence had been suggested by Franz Kurie in 1934.
Willard Frank Libby was an American physical chemist noted for his role in the 1949 development of radiocarbon dating, a process which revolutionized archaeology and palaeontology. For his contributions to the team that developed this process, Libby was awarded the Nobel Prize in Chemistry in 1960.
A radioactive tracer, radiotracer, or radioactive label is a synthetic derivative of a natural compound in which one or more atoms have been replaced by a radionuclide. By virtue of its radioactive decay, it can be used to explore the mechanism of chemical reactions by tracing the path that the radioisotope follows from reactants to products. Radiolabeling or radiotracing is thus the radioactive form of isotopic labeling. In biological contexts, experiments that use radioisotope tracers are sometimes called radioisotope feeding experiments.
Before Present (BP) or "years before present (YBP)" is a time scale used mainly in archaeology, geology, and other scientific disciplines to specify when events occurred relative to the origin of practical radiocarbon dating in the 1950s. Because the "present" time changes, standard practice is to use 1 January 1950 as the commencement date (epoch) of the age scale, with 1950 being labelled as the "standard year". The abbreviation "BP" has been interpreted retrospectively as "Before Physics", which refers to the time before nuclear weapons testing artificially altered the proportion of the carbon isotopes in the atmosphere, which scientists must account for.
Accelerator mass spectrometry (AMS) is a form of mass spectrometry that accelerates ions to extraordinarily high kinetic energies before mass analysis. The special strength of AMS among the different methods of mass spectrometry is its ability to separate a rare isotope from an abundant neighboring mass. The method suppresses molecular isobars completely and in many cases can also separate atomic isobars. This makes possible the detection of naturally occurring, long-lived radio-isotopes such as 10Be, 36Cl, 26Al and 14C.
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.
There are 40 known isotopes of iodine (53I) from 108I to 147I; all undergo radioactive decay except 127I, which is stable. Iodine is thus a monoisotopic element.
Carbon (6C) has 14 known isotopes, from 8
C
to 20
C
as well as 22
C
, of which 12
C
and 13
C
are stable. The longest-lived radioisotope is 14
C
, with a half-life of 5.70(3)×103 years. This is also the only carbon radioisotope found in nature, as trace quantities are formed cosmogenically by the reaction 14
N
+
n
→ 14
C
+ 1
H
. The most stable artificial radioisotope is 11
C
, which has a half-life of 20.3402(53) min. All other radioisotopes have half-lives under 20 seconds, most less than 200 milliseconds. The least stable isotope is 8
C
, with a half-life of 3.5(1.4)×10−21 s. Light isotopes tend to decay into isotopes of boron and heavy ones tend to decay into isotopes of nitrogen.
An isotopic signature is a ratio of non-radiogenic 'stable isotopes', stable radiogenic isotopes, or unstable radioactive isotopes of particular elements in an investigated material. The ratios of isotopes in a sample material are measured by isotope-ratio mass spectrometry against an isotopic reference material. This process is called isotope analysis.
The environmental isotopes are a subset of isotopes, both stable and radioactive, which are the object of isotope geochemistry. They are primarily used as tracers to see how things move around within the ocean-atmosphere system, within terrestrial biomes, within the Earth's surface, and between these broad domains.
Environmental radioactivity is part of the overall background radiation and is produced by radioactive materials in the human environment. While some radioisotopes, such as strontium-90 (90Sr) and technetium-99 (99Tc), are only found on Earth as a result of human activity, and some, like potassium-40 (40K), are only present due to natural processes, a few isotopes, such as tritium (3H), result from both natural processes and human activities. The concentration and location of some natural isotopes, particularly uranium-238 (238U), can be affected by human activity, such as nuclear weapons testing, which caused a global fallout, with up to 2.4 million deaths by 2020.
The Suess effect is a change in the ratio of the atmospheric concentrations of heavy isotopes of carbon (13C and 14C) by the admixture of large amounts of fossil-fuel derived CO2, which contains no 14CO2 and is depleted in 13CO2 relative to CO2 in the atmosphere and carbon in the upper ocean and the terrestrial biosphere. It was discovered by and is named for the Austrian chemist Hans Suess, who noted the influence of this effect on the accuracy of radiocarbon dating. More recently, the Suess effect has been used in studies of climate change. The term originally referred only to dilution of atmospheric 14CO2 relative to 12CO2. The concept was later extended to dilution of 13CO2 and to other reservoirs of carbon such as the oceans and soils, again relative to 12C.
The 774–775 carbon-14 spike is an observed increase of around 1.2% in the concentration of the radioactive carbon-14 isotope in tree rings dated to 774 or 775 CE, which is about 20 times higher than the normal year-to-year variation of radiocarbon in the atmosphere. It was discovered during a study of Japanese cedar tree-rings, with the year of occurrence determined through dendrochronology. A surge in beryllium-10 (10Be), detected in Antarctic ice cores, has also been associated with the 774–775 event. The 774–775 CE carbon-14 spike is one of several Miyake events and it produced the largest and most rapid rise in carbon-14 ever recorded.
The oceanic carbon cycle is composed of processes that exchange carbon between various pools within the ocean as well as between the atmosphere, Earth interior, and the seafloor. The carbon cycle is a result of many interacting forces across multiple time and space scales that circulates carbon around the planet, ensuring that carbon is available globally. The Oceanic carbon cycle is a central process to the global carbon cycle and contains both inorganic carbon and organic carbon. Part of the marine carbon cycle transforms carbon between non-living and living matter.
Minze Stuiver was a Dutch geochemist who was at the forefront of geoscience research from the 1960s until his retirement in 1998. He helped transform radiocarbon dating from a simple tool for archaeology and geology to a precise technique with applications in solar physics, oceanography, geochemistry, and carbon dynamics. Minze Stuiver's research encompassed the use of radiocarbon (14C) to understand solar cycles and radiocarbon production, ocean circulation, lake carbon dynamics and archaeology as well as the use of stable isotopes to document past climate changes.
The variation in the 14
C/12
C ratio in different parts of the carbon exchange reservoir means that a straightforward calculation of the age of a sample based on the amount of 14
C it contains will often give an incorrect result. There are several other possible sources of error that need to be considered. The errors are of four general types:
The marine reservoir effect is a phenomenon affecting radiocarbon dating. Because much of the carbon consumed by organisms in the ocean is older than that consumed by organisms on land, samples from marine life and from organisms that consumed a lot of sea-based foods while alive may appear older when tested than they truly are. It is necessary to account for changes in the Earth's oceans to correct for the marine reservoir effect. The level of the effect on a particular sample varies significantly, depending on the body of water, and more locally on depths, upwelling currents, and freshwater discharges.