Radiocarbon dating - Wikipedia

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Gentry also finds a variation in the haloes leading him to conclude that the decay constants have not been constant in time. To get one part in 10 million of argon in a rock in a thousand years, we would only need to get one part in 10 billion entering the rock each year. As pointed out earlier, different radiometric dating methods agree with each other most of the time, over many thousands of measurements. In the process the paper refutes a number of misconceptions prevalent among Christians today. This amount of argon is enough to raise 20 times the volume of magma to a K-Ar age of million years, and probably times the volume of the magam to an age of 57 million years. Most people find the subject of radiometric dating too technical to understand. There are also mixing scenarios that can produce even super isochrons having invalid ages.

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They did claim to have found--and carbon-dated--collagen, no? By taking enough measurements of the concentrations of X, Y, and Z, we can solve for c1 and c2, and from c1 we can determine the radiometric age of the sample. The goal is to promote greater understanding on this issue, particularly for the Christian community. Both of these tend on the average to have wide biostrategraphic limits, meaning that a large spread of ages will be regarded as non-anomalous. Assuming a strictly literal interpretation of the week of creation, even if some of the generations were left out of the genealogies, the Earth would be less than ten thousand years old. Examples of a number of consistent dates derived from different methods are given. They did not look at the data and they never spoke with the researchers.

Radiocarbon dating has allowed key transitions in prehistory to be dated, such as the end of the last ice age , and the beginning of the Neolithic and Bronze Age in different regions. In , Martin Kamen and Samuel Ruben of the Radiation Laboratory at Berkeley began experiments to determine if any of the elements common in organic matter had isotopes with half-lives long enough to be of value in biomedical research. They synthesized 14 C using the laboratory's cyclotron accelerator and soon discovered that the atom's half-life was far longer than had been previously thought.

Korff , then employed at the Franklin Institute in Philadelphia , that the interaction of slow neutrons with 14 N in the upper atmosphere would create 14 C. In , Libby moved to the University of Chicago where he began his work on radiocarbon dating.

He published a paper in in which he proposed that the carbon in living matter might include 14 C as well as non-radioactive carbon. By contrast, methane created from petroleum showed no radiocarbon activity because of its age.

The results were summarized in a paper in Science in , in which the authors commented that their results implied it would be possible to date materials containing carbon of organic origin. Libby and James Arnold proceeded to test the radiocarbon dating theory by analyzing samples with known ages. For example, two samples taken from the tombs of two Egyptian kings, Zoser and Sneferu , independently dated to BC plus or minus 75 years, were dated by radiocarbon measurement to an average of BC plus or minus years.

These results were published in Science in In , Libby was awarded the Nobel Prize in Chemistry for this work. In nature, carbon exists as two stable, nonradioactive isotopes: The half-life of 14 C the time it takes for half of a given amount of 14 C to decay is about 5, years, so its concentration in the atmosphere might be expected to reduce over thousands of years, but 14 C is constantly being produced in the lower stratosphere and upper troposphere by cosmic rays , which generate neutrons that in turn create 14 C when they strike nitrogen 14 N atoms.

Once produced, the 14 C quickly combines with the oxygen in the atmosphere to form carbon dioxide CO 2. Carbon dioxide produced in this way diffuses in the atmosphere, is dissolved in the ocean, and is taken up by plants via photosynthesis. Animals eat the plants, and ultimately the radiocarbon is distributed throughout the biosphere. The ratio of 14 C to 12 C is approximately 1. The equation for the radioactive decay of 14 C is: During its life, a plant or animal is exchanging carbon with its surroundings, so the carbon it contains will have the same proportion of 14 C as the atmosphere.

Once it dies, it ceases to acquire 14 C , but the 14 C within its biological material at that time will continue to decay, and so the ratio of 14 C to 12 C in its remains will gradually decrease. The equation governing the decay of a radioactive isotope is: Measurement of N , the number of 14 C atoms currently in the sample, allows the calculation of t , the age of the sample, using the equation above.

The above calculations make several assumptions, such as that the level of 14 C in the atmosphere has remained constant over time. The calculations involve several steps and include an intermediate value called the "radiocarbon age", which is the age in "radiocarbon years" of the sample: Calculating radiocarbon ages also requires the value of the half-life for 14 C , which for more than a decade after Libby's initial work was thought to be 5, years.

For consistency with these early papers, and to avoid the risk of a double correction for the incorrect half-life, radiocarbon ages are still calculated using the incorrect half-life value. A correction for the half-life is incorporated into calibration curves, so even though radiocarbon ages are calculated using a half-life value that is known to be incorrect, the final reported calibrated date, in calendar years, is accurate.

When a date is quoted, the reader should be aware that if it is an uncalibrated date a term used for dates given in radiocarbon years it may differ substantially from the best estimate of the actual calendar date, both because it uses the wrong value for the half-life of 14 C , and because no correction calibration has been applied for the historical variation of 14 C in the atmosphere over time. Carbon is distributed throughout the atmosphere, the biosphere, and the oceans; these are referred to collectively as the carbon exchange reservoir, [21] and each component is also referred to individually as a carbon exchange reservoir.

The different elements of the carbon exchange reservoir vary in how much carbon they store, and in how long it takes for the 14 C generated by cosmic rays to fully mix with them. This affects the ratio of 14 C to 12 C in the different reservoirs, and hence the radiocarbon ages of samples that originated in each reservoir. There are several other possible sources of error that need to be considered. The errors are of four general types:. To verify the accuracy of the method, several artefacts that were datable by other techniques were tested; the results of the testing were in reasonable agreement with the true ages of the objects.

Over time, however, discrepancies began to appear between the known chronology for the oldest Egyptian dynasties and the radiocarbon dates of Egyptian artefacts. The question was resolved by the study of tree rings: Coal and oil began to be burned in large quantities during the 19th century.

Dating an object from the early 20th century hence gives an apparent date older than the true date. For the same reason, 14 C concentrations in the neighbourhood of large cities are lower than the atmospheric average. This fossil fuel effect also known as the Suess effect, after Hans Suess, who first reported it in would only amount to a reduction of 0. A much larger effect comes from above-ground nuclear testing, which released large numbers of neutrons and created 14 C.

From about until , when atmospheric nuclear testing was banned, it is estimated that several tonnes of 14 C were created. The level has since dropped, as this bomb pulse or "bomb carbon" as it is sometimes called percolates into the rest of the reservoir. Photosynthesis is the primary process by which carbon moves from the atmosphere into living things.

In photosynthetic pathways 12 C is absorbed slightly more easily than 13 C , which in turn is more easily absorbed than 14 C. This effect is known as isotopic fractionation.

At higher temperatures, CO 2 has poor solubility in water, which means there is less CO 2 available for the photosynthetic reactions. The enrichment of bone 13 C also implies that excreted material is depleted in 13 C relative to the diet.

The carbon exchange between atmospheric CO 2 and carbonate at the ocean surface is also subject to fractionation, with 14 C in the atmosphere more likely than 12 C to dissolve in the ocean.

This increase in 14 C concentration almost exactly cancels out the decrease caused by the upwelling of water containing old, and hence 14 C depleted, carbon from the deep ocean, so that direct measurements of 14 C radiation are similar to measurements for the rest of the biosphere.

Correcting for isotopic fractionation, as is done for all radiocarbon dates to allow comparison between results from different parts of the biosphere, gives an apparent age of about years for ocean surface water. The CO 2 in the atmosphere transfers to the ocean by dissolving in the surface water as carbonate and bicarbonate ions; at the same time the carbonate ions in the water are returning to the air as CO 2.

The deepest parts of the ocean mix very slowly with the surface waters, and the mixing is uneven. The main mechanism that brings deep water to the surface is upwelling, which is more common in regions closer to the equator. Upwelling is also influenced by factors such as the topography of the local ocean bottom and coastlines, the climate, and wind patterns.

Overall, the mixing of deep and surface waters takes far longer than the mixing of atmospheric CO 2 with the surface waters, and as a result water from some deep ocean areas has an apparent radiocarbon age of several thousand years. Upwelling mixes this "old" water with the surface water, giving the surface water an apparent age of about several hundred years after correcting for fractionation. The northern and southern hemispheres have atmospheric circulation systems that are sufficiently independent of each other that there is a noticeable time lag in mixing between the two.

This is probably because the greater surface area of ocean in the southern hemisphere means that there is more carbon exchanged between the ocean and the atmosphere than in the north. Since the surface ocean is depleted in 14 C because of the marine effect, 14 C is removed from the southern atmosphere more quickly than in the north. For example, rivers that pass over limestone , which is mostly composed of calcium carbonate , will acquire carbonate ions.

Similarly, groundwater can contain carbon derived from the rocks through which it has passed. Volcanic eruptions eject large amounts of carbon into the air. Dormant volcanoes can also emit aged carbon. If the dates for Akrotiri are confirmed, it would indicate that the volcanic effect in this case was minimal. Any addition of carbon to a sample of a different age will cause the measured date to be inaccurate.

Contamination with modern carbon causes a sample to appear to be younger than it really is: Samples for dating need to be converted into a form suitable for measuring the 14 C content; this can mean conversion to gaseous, liquid, or solid form, depending on the measurement technique to be used.

Before this can be done, the sample must be treated to remove any contamination and any unwanted constituents. Particularly for older samples, it may be useful to enrich the amount of 14 C in the sample before testing.

This can be done with a thermal diffusion column. Once contamination has been removed, samples must be converted to a form suitable for the measuring technology to be used. For accelerator mass spectrometry , solid graphite targets are the most common, although iron carbide and gaseous CO 2 can also be used. The quantity of material needed for testing depends on the sample type and the technology being used. There are two types of testing technology: For beta counters, a sample weighing at least 10 grams 0.

For decades after Libby performed the first radiocarbon dating experiments, the only way to measure the 14 C in a sample was to detect the radioactive decay of individual carbon atoms. Libby's first detector was a Geiger counter of his own design. He converted the carbon in his sample to lamp black soot and coated the inner surface of a cylinder with it.

This cylinder was inserted into the counter in such a way that the counting wire was inside the sample cylinder, in order that there should be no material between the sample and the wire. Libby's method was soon superseded by gas proportional counters , which were less affected by bomb carbon the additional 14 C created by nuclear weapons testing.

These counters record bursts of ionization caused by the beta particles emitted by the decaying 14 C atoms; the bursts are proportional to the energy of the particle, so other sources of ionization, such as background radiation, can be identified and ignored. The counters are surrounded by lead or steel shielding, to eliminate background radiation and to reduce the incidence of cosmic rays.

In addition, anticoincidence detectors are used; these record events outside the counter, and any event recorded simultaneously both inside and outside the counter is regarded as an extraneous event and ignored. The other common technology used for measuring 14 C activity is liquid scintillation counting, which was invented in , but which had to wait until the early s, when efficient methods of benzene synthesis were developed, to become competitive with gas counting; after liquid counters became the more common technology choice for newly constructed dating laboratories.

The counters work by detecting flashes of light caused by the beta particles emitted by 14 C as they interact with a fluorescing agent added to the benzene. Like gas counters, liquid scintillation counters require shielding and anticoincidence counters. For both the gas proportional counter and liquid scintillation counter, what is measured is the number of beta particles detected in a given time period.

This provides a value for the background radiation, which must be subtracted from the measured activity of the sample being dated to get the activity attributable solely to that sample's 14 C.

In addition, a sample with a standard activity is measured, to provide a baseline for comparison. The ions are accelerated and passed through a stripper, which removes several electrons so that the ions emerge with a positive charge. A particle detector then records the number of ions detected in the 14 C stream, but since the volume of 12 C and 13 C , needed for calibration is too great for individual ion detection, counts are determined by measuring the electric current created in a Faraday cup.

Any 14 C signal from the machine background blank is likely to be caused either by beams of ions that have not followed the expected path inside the detector, or by carbon hydrides such as 12 CH 2 or 13 CH. A 14 C signal from the process blank measures the amount of contamination introduced during the preparation of the sample. These measurements are used in the subsequent calculation of the age of the sample. The calculations to be performed on the measurements taken depend on the technology used, since beta counters measure the sample's radioactivity whereas AMS determines the ratio of the three different carbon isotopes in the sample.

To determine the age of a sample whose activity has been measured by beta counting, the ratio of its activity to the activity of the standard must be found. To determine this, a blank sample of old, or dead, carbon is measured, and a sample of known activity is measured. The additional samples allow errors such as background radiation and systematic errors in the laboratory setup to be detected and corrected for.

The results from AMS testing are in the form of ratios of 12 C , 13 C , and 14 C , which are used to calculate Fm, the "fraction modern". Both beta counting and AMS results have to be corrected for fractionation. The calculation uses Libby's half-life of 5, years, not the more accurate modern value of 5, years.

The reliability of the results can be improved by lengthening the testing time. Radiocarbon dating is generally limited to dating samples no more than 50, years old, as samples older than that have insufficient 14 C to be measurable.

Older dates have been obtained by using special sample preparation techniques, large samples, and very long measurement times. These techniques can allow measurement of dates up to 60, and in some cases up to 75, years before the present.

This was demonstrated in by an experiment run by the British Museum radiocarbon laboratory, in which weekly measurements were taken on the same sample for six months. The measurements included one with a range from about to about years ago, and another with a range from about to about Errors in procedure can also lead to errors in the results. The calculations given above produce dates in radiocarbon years: To produce a curve that can be used to relate calendar years to radiocarbon years, a sequence of securely dated samples is needed which can be tested to determine their radiocarbon age.

The study of tree rings led to the first such sequence: These factors affect all trees in an area, so examining tree-ring sequences from old wood allows the identification of overlapping sequences. In this way, an uninterrupted sequence of tree rings can be extended far into the past. The first such published sequence, based on bristlecone pine tree rings, was created by Wesley Ferguson. For example, for K-Ar dating, we have the following requirements:. There must have been no incorporation of Ar40 into the mineral at the time of crystallization or a leak of Ar40 from the mineral following crystallization.

The earth is supposed to be nearly 5 billion years old, and some of these methods seem to verify ancient dates for many of earth's igneous rocks. The answer is that these methods, are far from infallible and are based on three arbitrary assumptions a constant rate of decay, an isolated system in which no parent or daughter element can be added or lost, and a known amount of the daughter element present initially.

Heating and deformation of rocks can cause these atoms to migrate, and water percolating through the rocks can transport these substances and redeposit them. These processes correspond to changing the setting of the clock hands. Not infrequently such resetting of the radiometric clocks is assumed in order to explain disagreements between different measurements of rock ages.

It is known that neutrinos interact with atomic nucleii, so a larger density of neutrinos could have sped up radioactive decay and made matter look old in a hurry. Some more quotes from the same source:. In the lead-uranium systems both uranium and lead can migrate easily in some rocks, and lead volatilizes and escapes as a vapor at relatively low temperatures.

It has been suggested that free neutrons could transform Pb first to Pb and then to Pb, thus tending to reset the clocks and throw thorium-lead and uranium-lead clocks completely off, even to the point of wiping out geological time. Furthermore, there is still disagreement of 15 percent between the two preferred values for the U decay constant. Potassium volatilizes easily, is easily leached by water, and can migrate through the rocks under certain conditions.

Furthermore, the value of the decay constant is still disputed, although the scientific community seems to be approaching agreement. Historically, the decay constants used for the various radiometric dating systems have been adjusted to obtain agreement between the results obtained. Argon, the daughter substance, makes up about one percent of the atmosphere, which is therefore a possible source of contamination. However, since it is possible for argon to be formed in the rocks by cosmic radiation, the correction may also be in error.

Argon from the environment may be trapped in magma by pressure and rapid cooling to give very high erroneous age results.

Rubidium parent atoms can be leached out of the rock by water or volatilized by heat. All of these special problems as well as others can produce contradictory and erroneous results for the various radiometric dating systems.

So we have a number of mechanisms that can introduce errors in radiometric dates. Heating can cause argon to leave a rock and make it look younger. In general, if lava was heated after the initial flow, it can yield an age that is too young.

If the minerals in the lava did not melt with the lava, one can obtain an age that is too old. Leaching can also occur; this involves water circulating in rock that can cause parent and daughter elements to enter or leave the rock and change the radiometric age. Thus it is easy to rationalize any date that is obtained. If a date is too old, one can say that the mineral did not melt with the lava. Maybe it got included from surrounding rock as the lava flowed upward.

If the date is too young, one can say that there was a later heating event. One can also hypothesize that leaching occurred. But then it is claimed that we can detect leaching and heating. But how can we know that this claim is true, without knowing the history of rocks and knowing whether they have in fact experienced later heating or leaching? The problems are compounded because many of the parent and daughter substances are mobile, to some extent.

I believe that all parent substances are water soluble, and many of the daughter products as well. A few sources have said that Sr is mobile in rock to some extent. This could cause trouble for Rb-Sr dating. In fact, some sources say that Sr and Ar have similar mobilities in rock, and Ar is very mobile. Especially the gaseous radioactive decay byproducts such as argon, radon, and helium are mobile in rock.

So if a rock has tiny cracks permitting gas to enter or escape or permitting the flow of water, the radiometric ages could be changed substantially even without the rock ever melting or mixing. Now, there is probably not much argon in a rock to start with.

So the loss of a tiny amount of argon can have significant effects over long time periods. A loss of argon would make the rock look younger. In a similar way, argon could enter the rock from the air or from surrounding rocks and make it look older. And this can also happen by water flowing through the rock through tiny cracks, dissolving parent and daughter elements.

It would be difficult to measure the tiny changes in concentration that would suffice to make large changes in the radiometric ages over long time periods. I also question the assertion that argon, for example, is excluded from certain minerals when they crystallize and never enters later on. Geologists often say that ages that are too old are due to excess argon. So it must be possible for that excess argon to get in, even though the crystal is supposed to exclude it.

Here is one such reference, although this is to a mineral that does not exclude argon:. In a few cases, argon ages older than that of the Earth which violate local relative age patterns have even been determined for the mineral biotite.

Such situations occur mainly where old rocks have been locally heated, which released argon into pore spaces at the same time that new minerals grew.

Under favourable circumstances the isochron method may be helpful, but tests by other techniques may be required. For example, the rubidium-strontium method would give a valid isotopic age of the biotite sample with inherited argon. Another problem is that the crystal structure typically has imperfections and impurities. For example, different kinds of quartz have different colors due to various impurities that are included but not part of the repetitive unit of the quartz crystal.

So even if the crystal excludes the daughter element, it could be present in impurities. Thus crystals, as they form, may have tiny imperfections that accept parent and daughter products in the same ratios as they occur in the lava, so one can inherit ages from the lava into minerals in this way.

It is also possible that parent and daughter elements could be present in boundaries between regular crystal domains. I don't know how we can be sure that a crystal will exclude argon or other daughter substances except by growing it in the laboratory under many conditions. There can also be argon or other daughter products added from the air or from other rocks.

One could say that we can detect whether the daughter is embedded in the crystal structure or not. But this would require an atom by atom analysis, which I do not believe is practical. Why K-Ar dating is inaccurate Since K-Ar potassium-argon dating is one of the most prevalent techniques, some special commentary about it is in order.

Potassium is about 2. Argon is about 3. This is about one ten millionth of the mass of the rock, a very tiny percentage. And yet, with a large amount of argon in the air and also filtering up from rocks below, and with excess argon in lava, with argon and potassium water soluble, and argon mobile in rock, we are still expecting this wisp of argon to tell us how old the rock is!

The percentage of Ar40 is even less for younger rocks. For example, it would be about one in million for rocks in the vicinity of 57 million years old. To get one part in 10 million of argon in a rock in a thousand years, we would only need to get one part in 10 billion entering the rock each year. This would be less than one part in a trillion entering the rock each day, on the average. This would suffice to give a rock having an average concentration of potassium, a computed potassium-argon age of over million years!

We can also consider the average abundance of argon in the crust. This implies a radiometric age of over 4 billion years. So a rock can get a very old radiometric age just by having average amounts of potassium and argon.

It seems reasonable to me that the large radiometric ages are simply a consequence of mixing, and not related to ages at all, at least not necessarily the ages of the rocks themselves. The fact that not all of the argon is retained would account for smaller amounts of argon near the surface, as I will explain below. This could happen because of properties of the magma chambers, or because of argon being given off by some rocks and absorbed by others. I don't see how one can possibly know that there are no tiny cracks in rocks that would permit water and gas to circulate.

The rates of exchange that would mess up the dates are very tiny. It seems to me to be a certainty that water and gas will enter rocks through tiny cracks and invalidate almost all radiometric ages.

Let me illustrate the circulation patterns of argon in the earth's crust. So argon is being produced throughout the earth's crust, and in the magma, all the time. In fact, it probably rises to the top of the magma, artificially increasing its concentration there. Now, some rocks in the crust are believed not to hold their argon, so this argon will enter the spaces between the rocks. Leaching also occurs, releasing argon from rocks. Heating of rocks can also release argon.

Argon is released from lava as it cools, and probably filters up into the crust from the magma below, along with helium and other radioactive decay products. All of this argon is being produced and entering the air and water in between the rocks, and gradually filtering up to the atmosphere. But we know that rocks absorb argon, because correction factors are applied for this when using K-Ar dating.

So this argon that is being produced will leave some rocks and enter others. The partial pressure of argon should be largest deepest in the earth, and decrease towards the surface. This would result in larger K-Ar ages lower down, but lower ages nearer the surface. So this confirms that argon can travel from rock to rock when one rock is heated. Now, argon is very soluble in magma, which can hold a lot of it:. After the material was quenched, the researchers measured up to 0.

They noted, 'The solubility of Ar in the minerals is surprisingly high'. I note that this concentration of argon, if it were retained in the rock, would suffice to give it a geological age well over nillion years, assuming an average concentration of potassium. This is from a paper by Austin available at ICR. This paper also discusses Mount St. Helens K-Ar dating, and historic lava flows and their excess argon.

So magma holds tremendous amounts of argon. Now, consider an intrusive flow, which cools within the earth. All its argon will either remain inside and give an old age to the flow, or will travel through surrounding rock, where it can be absorbed by other rocks. So magma should have at least 20 times as much argon as a rock million years old by K-Ar dating. In fact, the argon in the magma may well be even higher, as it may concentrate near the top.

This amount of argon is enough to raise 20 times the volume of magma to a K-Ar age of million years, and probably times the volume of the magam to an age of 57 million years.

So one sees that there is a tremendous potential for age increases in this way. It is not necessary for this increase in age to happen all at once; many events of this nature can gradually increase the K-Ar ages of rocks. In general, older rocks should have more argon because they have been subject to more exposure to such argon, but their true age is not necessarily related to their K-Ar radiometric age. We can also consider that most volcanoes and earthquakes occur at boundaries between plates, so if the lava has flowed before, it is likely to flow again nearby, gradually increasing the age.

I suppose earthquakes could also allow the release of argon from the magma. Other mechanisms include dissolving of rock, releasing its argon, fracturing of rock, with release of argon, argon from cooling lava under water entering the water and entering other rocks, and argon from cooling lave entering subterranean water and being transported to other rock.

There are so many mechanisms that it is hard to know what pattern to expect, and one does not need to rely on any one of them such as more argon in the magma in the past to account for problems in K-Ar dating. Since even rocks with old K-Ar dates still absorb more argon from the atmosphere in short time periods, it follows that rocks should absorb quite a bit of argon over long time periods, especially at higher pressures.

In fact, if a rock can absorb only a ten millionth part of argon, that should be enough to raise its K-Ar age to over million years, assuming an average amounts of potassium. It wouldn't require many internal cracks to allow a ten millionth part of argon to enter. Also, as the rock deforms under pressure, more cracks are likely to form and old ones are likely to close up, providing more opportunity for argon and other gases to enter.

I mentioned a number of possibilities that could cause K-Ar dates to be much older than the true ages of the rocks. Here is another way that K-Ar dates can be too old: If we assume the earth went through a catastrophe recently, then the crustal plates might have been agitated, permitting lava and argon to escape from the magma.

Thus a lot of argon would be filtering up through the crust. As intrusive flows of lava cooled inside the crust, they would have been in an environment highly enriched in argon, and thus would not have gotten rid of much of their argon. Thus they would have hardened with a lot of argon inside.

This would make them appear old. The same goes for extrusive flows on the surface, since argon would be filtering up through the earth and through the lava as it cooled. In areas where tremendous tectonic activity has taken place, highly discordant values for the ages are obtained. The difficulties associated are numerous and listed as follows:. There seems to be a great deal of question regarding the branching ratio for K40 into Ar40 and Ca But the value is not really known.

The observed value is between 0. However, this doesn't remedy the situation and the ages are still too high [low? The geochronologists credit this to "argon leakage". There is far too much Ar40 in the earth for more than a small fraction of it to have been formed by radioactive decay of K This is true even if the earth really is 4.

In the atmosphere of the earth, Ar40 constitutes This is around times the amount that would be generated by radioactive decay over the age of 4.

Certainly this is not produced by an influx from outer space. Thus, a large amount of Ar40 was present in the beginning. Since geochronologists assume that errors due to presence of initial Ar40 are small, their results are highly questionable. Argon diffuses from mineral to mineral with great ease. It leaks out of rocks very readily and can move from down deep in the earth, where the pressure is large, and accumulate in an abnormally large amount in the surface where rock samples for dating are found.

They would all have excess argon due to this movement. This makes them appear older. Rocks from deeper in the crust would show this to a lesser degree. Also, since some rocks hold the Ar40 stronger than others, some rocks will have a large apparent age, others smaller ages, though they may actually be the same age.

If you were to measure Ar40 concentration as function of depth, you would no doubt find more of it near the surface than at deeper points because it migrates more easily from deep in the earth than it does from the earth into the atmosphere. It is easy to see how the huge ages are being obtained by the KAr40 radiometric clock, since surface and near-surface samples will contain argon due to this diffusion effect.

Some geochronologists believe that a possible cause of excess argon is that argon diffuses into mineral progressively with time. Significant quantities of argon may be introduced into a mineral even at pressures as low as one bar. If such [excessive] ages as mentioned above are obtained for pillow lavas, how are those from deep-sea drilling out in the Atlantic where sea-floor spreading is supposed to be occurring? Potassium is found to be very mobile under leaching conditions.

This could move the "ages" to tremendously high values. Ground-water and erosional water movements could produce this effect naturally.

Rocks in areas having a complex geological history have many large discordances. In a single rock there may be mutually contaminating, potassium- bearing minerals. There is some difficulty in determining the decay constants for the KAr40 system.

Geochronologists use the branching ratio as a semi-emperical, adjustable constant which they manipulate instead of using an accurate half-life for K A number of recent lava flows within the past few hundred years yield potassium-argon ages in the hundreds of thousands of years range. This indicates that some excess argon is present. Where is it coming from? And how do we know that it could not be a much larger quantity in other cases?

If more excess argon were present, then we could get much older ages. It is true that an age difference in the hundreds of thousands of years is much too small to account for the observed K-Ar ages. But excess argon is commonly invoked by geologists to explain dates that are too old, so I'm not inventing anything new. Second, there may have been a lot more more argon in the magma in the past, and with each eruption, the amount decreased.

So there would have been a lot more excess argon in the past, leading to older ages. For rocks that are being dated, contamination with atmospheric argon is a persistent problem that is mentioned a number of times. Thus it is clear that argon enters rock easily. It is claimed that we can know if a rock has added argon by its spectrum when heated; different temperatures yield different fractions of argon. It is claimed that the argon that enters from the atmosphere or other rocks, is less tightly bound to the crystal lattice, and will leave the rock at a lower temperature.

But how do we know what happens over thousands of years? It could be that this argon which is initially loosely bound if it is so initially gradually becomes more tightly bound by random thermal vibrations, until it becomes undetectable by the spectrum technique. The fact that rock is often under high pressure might influence this process, as well. The branching ratio problem We now consider in more detail one of the problems with potassium-argon dating, namely, the branching ratio problem.

Here is some relevant information that was e-mailed to me. There are some very serious objections to using the potassium-argon decay family as a radiometric clock. The geochronologist considers the Ca40 of little practical use in radiometric dating since common calcium is such an abundant element and the radiogenic Ca40 has the same atomic mass as common calcium. Here the actual observed branching ratio is not used, but rather a small ratio is arbitrarily chosen in an effort to match dates obtained method with U-Th-Pb dates.

The branching ratio that is often used is 0. Thus we have another source of error for K-Ar dating. Henke criticized some statements in my article taken from Slusher about the branching ratio for potassium.

Slusher asserted that the best known value of the branching ratio was not always used in computing K-Ar radiometric ages. Unfortunately, Dalrymple says nothing about the calculation of the branching ratio. He simply gives the correct value for the K-Ar system. The issue is not just how well this was known in the past, but which value was actually used, and whether dates published in the past have been computed with the most recent value.

Often values for constants are standardized, so that the values actually used may not be the most accurate known. All that Dalrymple says is that his ages were all recomputed using the most accurate values of the constants. This implies that some of them were originally computed using less accurate values, which is similar to Slusher's point.

He admits that Slusher's statements about it would have been true in the 's and early 's, but are no longer true. But he didn't say when the correct value for the branching ratio began to be used. Even some figures from Faure, Principles of Isotope Geology, are based on another constant that is 2 or 3 percent too low, according to Dalrymple, and so there may be many ages in the literature that need revision by small amounts.

However, Harland et al imply that nearly the correct value for the branching ratio has been known and used since the mid-fifties. We now consider whether they can explain the observed dates. In general, the dates that are obtained by radiometric methods are in the hundreds of millions of years range. One can understand this by the fact that the clock did not get reset if one accepts the fact that the magma "looks" old, for whatever reason.

That is, we can get both parent and daughter elements from the magma inherited into minerals that crystallize out of lava, making these minerals look old. Since the magma has old radiometric dates, depending on how much the clock gets reset, the crust can end up with a variety of younger dates just by partially inheriting the dates of the magma.

Thus any method based on simple parent to daughter ratios such as Rb-Sr dating is bound to be unreliable, since there would have to be a lot of the daughter product in the magma already. And Harold Coffin's book Creation by Design lists a study showing that Rb-Sr dates are often inherited from the magma.

Even the initial ratios of parent and daughter elements in the earth do not necessarily indicate an age as old as 4. Radioactive decay would be faster in the bodies of stars, which is where scientists assume the heavy elements formed. Imagine a uranium nucleus forming by the fusion of smaller nucleii. At the moment of formation, as two nucleii collide, the uranium nucleus will be somewhat unstable, and thus very likely to decay into its daughter element.

The same applies to all nucleii, implying that one could get the appearance of age quickly. Of course, the thermonuclear reactions in the star would also speed up radioactive decay.

But isochrons might be able to account for pre-existing daughter elements. Furthermore, some elements in the earth are too abundant to be explained by radioactive decay in 4. Some are too scarce such as helium. So it's not clear to me how one can be sure of the 4. Why older dates would be found lower in the geologic column especially for K-Ar dating In general, potassium-argon dates appear to be older the deeper one goes in the crust of the earth.

We now consider possible explanations for this. There are at least a couple of mechanisms to account for this. In volcano eruptions, a considerable amount of gas is released with the lava. This gas undoubtedly contains a significant amount of argon Volcanos typically have magma chambers under them, from which the eruptions occur.

It seems reasonable that gas would collect at the top of these chambers, causing artificially high K-Ar radiometric ages there. In addition, with each successive eruption, some gas would escape, reducing the pressure of the gas and reducing the apparent K-Ar radiometric age. Thus the decreasing K-Ar ages would represent the passage of time, but not necessarily related to their absolute radiometric ages.

As a result, lava found in deeper layers, having erupted earlier, would generally appear much older and lava found in higher layers, having erupted later, would appear much younger.

This could account for the observed distribution of potassium-argon dates, even if the great sedimantary layers were laid down very recently. In addition, lava emerging later will tend to be hotter, coming from deeper in the earth and through channels that have already been warmed up. This lava will take longer to cool down, giving more opportunity for enclosed argon to escape and leading to younger radiometric ages.

Another factor is that rocks absorb argon from the air. It is true that this can be accounted for by the fact that argon in the air has Ar36 and Ar40, whereas only Ar40 is produced by K-Ar decay. But for rocks deep in the earth, the mixture of argon in their environment is probably much higher in Ar40, since only Ar40 is produced by radioactive decay. As these rocks absorb argon, their radiometric ages would increase.

This would probably have a larger effect lower down, where the pressure of argon would be higher. Or it could be that such a distribution of argon pressures in the rocks occurred at some time in the past. This would also make deeper rocks tend to have older radiometric ages. Recent lava flows often yield K-Ar ages of about , years. This shows that they contain some excess argon, and not all of it is escaping. If they contained a hundred times more excess argon, their K-Ar ages would be a hundred times greater, I suppose.

And faster cooling could increase the ages by further large factors. I also read of a case where a rock was K-Ar dated at 50 million years, and still susceptible to absorbing argon from the air. This shows that one might get radiometric ages of at least 50 million years in this way by absorbing Ar40 deep in the earth without much Ar36 or Ar38 present. If the pressure of Ar40 were greater, one could obtain even greater ages. Yet another mechanism that can lead to decreasing K-Ar ages with time is the following, in a flood model: One can assume that at the beginning of the flood, many volcanoes erupted and the waters became enriched in Ar Then any lava under water would appear older because its enclosed Ar40 would have more trouble escaping.

As time passed, this Ar40 would gradually pass into the atmosphere, reducing this effect and making rocks appear younger. In addition, this would cause a gradient of Ar40 concentrations in the air, with higher concentrations near the ground.

This also could make flows on the land appear older than they are, since their Ar40 would also have a harder time escaping. Plaisted wants to give his readers the impression that argon can readily move in and out of minerals and, therefore, the gas is too volatile for radiometric dating. Specifically, he quotes one of his anonymous friends that claims that argon easily diffuses from minerals p. Of course, these statements are inaccurate generalizations. Geochronologists are aware that excess argon may accumulate on mineral surfaces and the surface argon would be removed before analysis.

However, Henke admits that this can happen in some cases. He states that geologists are aware of this problem, and make allowances for it. But it is more difficult to remove argon that has deposited on cracks in the mineral, which can be difficult to see. Henke referenced Davis A. Young frequently, but I was not able to find Young referenced in any of the other sources I examined except Dalrymple Henke states that hornblendes retain argon very well, but then later says that they can easily absorb excess argon.

Geologists also recognize that heating causes argon to leave minerals, and that dissolved argon in a mineral that does not escape will become incorporated into it, artificially increasing its K-Ar age. I will comment more on this below, but a few comments now are appropriate. For a temperature of K 27 degrees C , there is no significant argon loss from biotite. At K degrees C , there is a slow but significant diffusion rate.

At K degrees C , loss of argon is quite rapid. To lose one percent in one year requires a temperature of nearly degrees centigrade. Thus the temperature does not have to be very high for argon to move through rock. This also justifies Slusher's statements about argon moving in and out of rocks with ease. However, it does not seem likely that sedimentary rocks would be this hot very often, except near lava or magma flows. But argon does not need to move through all rock in order to influence radiometric dates, it only has to reach ancient lava flows.

This it can do by following the path of the ancient lava flow itself, coming up along the path of the magma. As the magma or lava cools, this path will consist entirely of hot magma or lava, and so the argon will have a free path, and will continue to enter the magma as it cools. Thus in many cases, the lava or magma will never completely degas, and extra argon will end up trapped in the cooled rock.

This will result in artificially increased K-Ar ages. Many ancient lava flows are relatively flat, in contrast to modern ones. Also, they appear to have been covered over quickly. The flatness means that the lava is a contiguous mass, and can still be reached from the hot magma by a continuous path of hot rock. The fact that they soon are covered over means that the argon has a hard time escaping vertically from the lava, so argon coming up from the mantle will tend to enter the cooling rock.

Both facts will tend to produce artificially high K-Ar ages in these flows which will not be seen in modern lava flows in the same manner.

Modern lava flows often come down the sides of volcanoes, and thus become separated from their source by large distances. Also, they do not get quickly buried by additional sediment. Thus modern lava flows are not subject to the same mechanism of artificial increases in their K-Ar ages as are ancient ones.

Also, it is reasonable to assume that as argon leaves the mantle in successive eruptions, the amount of argon remaining is reduced, so that later lava flows are less susceptible to such artificial increases in age. The path of magma also becomes longer for later flows, and the magma probably also is a little cooler, inhibiting argon flow.

Thus later lava flows give younger K-Ar ages. Another point to note is that even after it cools, the lava or magma may still have many cracks in it, permitting argon to flow. This argon will tend to deposit on the surface of minerals, but with the passage of time it will tend to diffuse into the interior, even if only a very small distance. This is especially true as the lava is cooling. This will make it more difficult to detect this added argon by the spectrum test described below.

Also, the diffusion of argon in cracks and channels of a mineral is likely much less temperature-dependent than diffusion through unbroken regions of the mineral, since diffusion through cracks and channels simply involves jumps through the air.

By a combination of diffusion through cracks and channels, and short passages through unbroken regions of the mineral, argon may be able to reach a considerable distance into the mineral.

At low temperatures, this may become the dominant means by which argon diffuses into a mineral, but the effect of this kind of diffusion at low temperatures may not be evident until many years have passed. Thus it may take experiments lasting 50 or years at low temperatures to detect the effects of this kind of diffusion of argon, which however could be significantly increasing the K-Ar ages of minerals over long time periods.

Dickin Radiogenic Isotope Geology, , p. It has been claimed that this can be accomplished by preheating samples under vacuum or by leaching them briefly with hydroflouric acid, or both However Armstrong has questioned whether atmospheric argon, that has been acquired by minerals over a long interval of time, can be removed by this method.

Thus there is some means by which argon from outside can become very firmly embedded within a rock, and one would expect that the quantity of this argon would continue to increase over time, giving anomalously old K-Ar ages. Added atmospheric argon can be detected, because the ratio of argon 40 to argon 36 for atmospheric argon is But argon 40 coming up from the mantle and diffusing into a mineral would not be detectable in this way, because it has a higher ratio of argon 40 to argon This shows that rocks can adsorb a large amount of argon relative to the argon needed to give them old K-Ar ages, and also suggests that old K-Ar ages can be produced by external argon from the mantle.

Over a long period of time, adsorbed argon will tend to diffuse into the rock, and thus it will be possible for even more argon to be deposited on the surface, increasing K-Ar ages even more.

Generally, excess 40Ar is observed in minerals that have been exposed to a high partial pressure of argon during regional metamorphism, in pegmatites The argon that may either diffuse into the minerals or may be occluded within them is derived by outgassing of K-bearing minerals in the crust and mantle of the Earth. The presence of excess 40Ar increases K-Ar dates and may lead to overestimates of the ages of minerals dated by this method. Let us consider the question of how much different dating methods agree on the geologic column, and how many measurements are anomalous, since these points are often mentioned as evidences of the reliability of radiometric dating.

It takes a long time to penetrate the confusion and find out what is the hard evidence in this area. In the first place, I am not primarily concerned with dating meteorites, or precambrian rocks. What I am more interested in is the fossil-bearing geologic column of Cambrian and later age.

Now, several factors need to be considered when evaluating how often methods give expected ages on the geologic column. Some of these are taken from John Woodmoreappe's article on the subject, but only when I have reason to believe the statements are also generally believed.

First, many igneous formations span many periods, and so have little constraint on what period they could belong to. The same applies to intrusions. In addition, some kinds of rocks are not considered as suitable for radiometric dating, so these are typically not considered. Furthermore, it is at least possible that anomalies are under-reported in the literature. Finally, the overwhelming majority of measurements on the fossil bearing geologic column are all done using one method, the K-Ar method.

And let me recall that both potassium and argon are water soluble, and argon is mobile in rock. Thus the agreement found between many dates does not necessarily reflect an agreement between different methods, but rather the agreement of the K-Ar method with itself.

For example, if 80 percent of the measurements were done using K-Ar dating, and the other 20 percent gave random results, we still might be able to say that most of the measurements on a given strata agree with one another reasonably well. So to me it seems quite conceivable that there is no correlation at all between the results of different methods on the geologic column, and that they have a purely random relationship to each other.

Let us consider again the claim that radiometric dates for a given geologic period agree with each other. I would like to know what is the exact or approximate information content of this assertion, and whether it could be or has been tested statistically.

It's not as easy as it might sound. Let's suppose that we have geologic periods G Let's only include rocks whose membership in the geologic period can be discerned independent of radiometric dating methods.

Let's also only include rocks which are considered datable by at least one method, since some rocks I believe limestone are considered not to hold argon, for example.

Now, we can take a random rock from Gi. We will have to restrict ourselves to places where Gi is exposed, to avoid having to dig deep within the earth. Let's apply all known dating methods to Gi that are thought to apply to this kind of rock, and obtain ages from each one. Then we can average them to get an average age for this rock.

We can also compute how much they differ from one another. Now we have to be careful about lava flows -- which geologic period do they belong to? What about rocks that are thought not to have their clock reset, or to have undergone later heating episodes? Just to make the test unbiased, we will assign altitude limits to each geologic period at each point on the earth's surface at least in principle and include all rocks within these altitude limits within Gi, subject to the condition that they are datable.

For each geologic period and each dating method, we will get a distribution of values. We will also get a distribution of averaged values for samples in each period. Now, some claim is being made about these distributions. It is undoubtedly being claimed that the mean values ascend as one goes up the geologic column. It is also being claimed that the standard deviations are not too large.

It is also being claimed that the different methods have distributions that are similar to one another on a given geologic period. The only correlation I know about that has been studied is between K-Ar and Rb-Sr dating on precambrian rock. And even for this one, the results were not very good. This was a reference by Hurley and Rand, cited in Woodmorappe's paper.

As far as I know, no study has been done to determine how different methods correlate on the geologic column excluding precambrian rock.

The reason for my request is that a correlation is not implied by the fact that there are only 10 percent anomalies, or whatever. I showed that the fact that the great majority of dates come from one method K-Ar and the fact that many igneous bodies have very wide biostratigraphic limits, where many dates are acceptable, makes the percentage of anomalies irrelevant to the question I am asking.

And since this agreement is the strongest argument for the reliability of radiometric dating, such an assumption of agreement appears to be without support so far. The question of whether different methods correlate on the geologic column is not an easy one to answer for additional reasons.

Since the bulk of K-Ar dates are generally accepted as correct, one may say that certain minerals are reliable if they tend to give similar dates, and unreliable otherwise. We can also say that certain formations tend to give reliable dates and others do not, depending on whether the dates agree with K-Ar dates. Thus we can get an apparent correlation of different methods without much of a real correlation in nature.

It's also possible for other matter to be incorporated into lava as it rises, without being thoroughly melted, and this matter may inherit all of its old correlated radiometric dates. Coffin mentions that fission tracks can survive transport through lava, for example. It may also be that lava is produced by melting the bottom of continents and successively different layers are melted with time, or there could be a tendency for lighter isotopes to come to the top of magma chambers, making the lava there appear older.

But anyway, I think it is important really to know what patterns appear in the data to try to understand if there is a correlation and what could be causing it. Not knowing if anomalies are always published makes this harder. It is often mentioned that different methods agree on the K-T boundary, dated at about 65 million years ago. This is when the dinosaurs are assumed to have become extinct. This agreement of different methods is taken as evidence for a correlation between methods on the geologic column.

One study found some correlated dates from bentonite that are used to estimate the date of the K-T boundary. I looked up some information on bentonite.

It is composed of little glass beads that come from volcanic ash. This is formed when lava is sticky and bubbles of gas in it explode. So these small particles of lava cool very fast. The rapid cooling might mean that any enclosed argon is retained, but if not, the fact that this cooling occurs near the volcano, with a lot of argon coming out, should guarantee that these beads would have excess argon. As the gas bubble explodes, its enclosed argon will be rushing outward along with these tiny bubbles as they cool.

This will cause them to retain argon and appear too old. In addition, the rapid cooling and the process of formation means that these beads would have Rb, Sr, U, and Pb concentrations the same as the lava they came from, since there is no chance for crystals to form with such rapid cooling.

So to assume that the K-Ar dates, Rb-Sr dates, and U-Pb dates all reflect the age of the lava, one would have to assume that this lava had no Sr, no Pb, and that all the argon escaped when the beads formed. Since the magma generally has old radiometric ages, I don't see how we could have magma without Pb or Sr. So to me it seems to be certain that these ages must be in error. Furthermore, the question arises whether bentonite always gives correlated ages, and whether these ages always agree with the accepted ages for their geologic period.

I believe that bentonite occurs in a number of formations of different geologic periods, so this could be checked. If bentonite does not always give correlate and correct ages, this calls into question its use for dating the K-T boundary. Let me briefly comment on a couple of other articles at Tim Thompson's page. This is at least close to what I am looking for. However, it would be better to date all five craters by all four different methods, and see what the agreement is.

It is also possible that each crater gives a scatter of dates, and the best ones were selected. Furthermore, it is possible that the craters were chosen as those for which the dating methods agreed. Possible other sources of correlation Note that if there are small pockets in crystals where both parent and daughter product can accumulate from the lava, then one can inherit correlated ages from the lava into minerals.

Thus even the existence of correlations is not conclusive evidence that a date is correct. Anomalies of radiometric dating If a date does not agree with the expected age of its geologic period, and no plausible explanation can be found, then the date is called anomalous.

But if we really understand what is going on, then we should be able to detect discrepant dates as they are being measured, and not just due to their divergence from other dates.

Geologists often say that the percentage of anomalies is low. But there are quite a number of rather outstanding anomalies in radiometric dating that creationists have collected. These anomalies are reported in the scientific literature. For example, one isochron yielded a date of 10 billion years.

A Rb-Sr isochron yielded a date of 34 billion years. K-Ar dates of 7 to 15 billion years have been recorded. It's also not uncommon for two methods to agree and for the date to be discarded anyway. Samples with flat plateaus which should mean no added argon can give wrong dates. Samples giving no evidence of being disturbed can give wrong dates.

Samples that give evidence of being disturbed can give correct dates. The number of dates that disagree with the expected ages is not insignificant. I don't know what the exact percentage is. Many dates give values near the accepted ones. But even these often differ from one another by 10 or 20 percent. And quite a few other dates are often much, much farther off. Whatever is making some of these dates inaccurate could be making all of them inaccurate. Age estimates on a given geological stratum by different radiometric methods are often quite different sometimes by hundreds of millions of years.

There is not absolutely reliable long-term radiological "clock". The uncertainties inherent in radiometric dating are disturbing to geologists and evolutionists As proof of the unreliability of the radiometric methods consider the fact that in nearly every case dates from recent lava flows have come back excessively large. One example is the rocks from the Kaupelehu Flow, Hualalai Volcano in Hawaii which was known to have erupted in These rocks were dated by a variety of different methods.

Of 12 dates reported the youngest was million years and the oldest was 2. The dates average 1. Another source said that about 5 or 6 of the historic lava flows give ages in the hundreds of thousands of years.

Geologists explain the Kaupelehu date by the lava being cooled rapidly in deep ocean water and not being able to get rid of its enclosed argon. Instead, the uncertainty grows as more and more data is accumulated Woodmorappe also mentions that very self-contradictory age spreads in the Precambrian era are common. In addition, Woodmorappe gives over sets of dates "that are in gross conflict with one another and with expected values for their indicated paleontological positions.

This does not include dates from minerals that are thought to yield bad dates, or from igneous bodies with wide biostrategraphic ranges, where many dates are acceptable. He states that the number of dates within range are less than the number of anomalies, except for the Cenozoic and Cretaceous. When one adds in the fact that many anomalies are unreported, which he gives evidence for, the true distribution is anyone's guess. There have been criticisms of John Woodmorappe's study, but no one has given any figures from the literature for the true percentage of anomalies, with a definition of an anomaly, or the degree of correlation between methods.

Steven Schimmrich's review of this study often concerns itself with John W's presentation of geologists explanation for anomalies, and not with the percentage of anomalies; the later is my main concern. The carbon age of the buried trees is only years, but some of the overlying volcanic material has a ,year potassium-argon age. A similar situation is reported in the December issue of Creation ex nihilo in which lava with a K-Ar age of about 45 million years overlays wood that was carbon dated by 3 laboratories using AMS dating to about 35, years.

Still another evidence for problems with radiometric dating was given in a recent talk I attended by a man who had been an evolutionist and taken a course in radiometric dating. The teacher gave 14 assumptions of radiometric dating and said something like "If creationists got a hold of these, they could cut radiometric dating to pieces.

Another evidence that all is not well with radiometric dating is given in the following quote from Coffin p. Many sedimentary uranium ores are not. Since equilibrium should be reached in 1 million years, this is a problem for sediments that are assumed to be older than 1 million years. On another point, if we can detect minerals that were not molten with the lava, as has been claimed, then this is one more reason why there should be no anomalies, and radiometric dating should be a completely solved problem.

But that does not appear to be the case, at least especially on the geologic column. I'm not claiming that anomalous results are being hidden, just that the agreement of a mass of results, none of which has much claim to reliability, does not necessarily mean much.

Picking out a few cases where radiometric dates appear to be well-behaved reminds me of evolutionary biologists focusing on a few cases where there may be transitional sequences.

It does not answer the overall question. And as I said above, I'm also interested to know how much of the fossil-bearing geologic column can be dated by isochrons, and how the dates so obtained compare to others.

Gerling et al called attention to some chlorites yielding K-Ar dates of 7 to 15 b. It had been noted that some minerals which yield such dates as beryl, cordierite, etc. They also pointed out that for the anomalies to be accounted for by excess argon, unreasonably high partial pressures of Ar during crystallization would have to be required.

They concluded by suggesting some unknown nuclear process which no longer operates to have generated the Ar. This implies that excess argon is coming from somewhere. Here is another quote from Woodmorappe about isochrons, since some people think that mixing scenarios or other age-altering scenarios are unlikely:. If this condition does not hold, invalid ages and intercepts are obtained.

Models yield isochron ages that are too high, too low, or in the future, sometimes by orders of magnitude. The fact that the only "valid" K-Ar isochrons are those for which the concentration of non-radiogenic argon Ar36 is constant, seems very unusual. This suggests that what is occuring is some kind of a mixing phenomenon, and not an isochron reflecting a true age. We have analyzed several devitrified glasses of known age, and all have yielded ages that are too young.

Some gave virtually zero ages, although the geologic evidence suggested that devitrification took place shortly after the formation of a deposit.

Why a low anomaly percentage is meaningless One of the main arguments in favor of radiometric dating is that so many dates agree with each other, that is, with the date expected for their geologic period.

But it's not evident how much support this gives to radiometric dating. If a rock dates too old, one can say that the clock did not get reset. If it dates too young, one can invoke a later heating event. Neither date would necessarily be seen as anomalous. If lava intrudes upon geologic period X, then any date for the lava of X or later will not be seen as anomalous.

And even if the date is one or two geologic periods earlier, it may well be close enough to be accepted as non-spurious. If one does not know the geologic period of a rock by other means, then of course one is likely to date it to find out, and then of course the date agrees with the geologic period and this will not be seen as anomalous.

Imsges: what is carbon dating how is the age of fossils determined

what is carbon dating how is the age of fossils determined

Wiens wrote the first edition of this paper while in Pasadena.

what is carbon dating how is the age of fossils determined

Dates from anywhere between twenty to one thousand million years ago can be determined with this particular technique. No, his objection was that the Paleochronology group was using the reports as evidence that dinosaurs lived thousands, not millions, of years ago.

what is carbon dating how is the age of fossils determined

In MarchDr. Alpha decay is most common in heavy elements. Harold examined at length the current state of origin-of-life research in a chapter titled "Ultimate Riddle - Origin of Cellular Life" in his book "In Search of Cell History: For example, most people don't realize that carbon dating is only rarely used on rocks. Further evidence comes from wht complete agreement between radiometric dates and other dating methods such as counting tree rings deyermined glacier ice core layers. What is carbon dating how is the age of fossils determined, at least for uranium-lead dating, a kind of isochron has been observed among five meteorites containing uranium and a number which do not, which gives a rational basis for assuming how much daughter product was present initially.