Actual measurement of radioactive decay

Click For Summary

Discussion Overview

The discussion revolves around the practical aspects of measuring radioactive decay, specifically focusing on carbon-14 dating and its application in fields such as anthropology, archaeology, and geology. Participants explore the methodologies involved in determining the age of samples and the challenges associated with contamination and measurement techniques.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • One participant seeks clarification on how scientists measure carbon-14 in samples and expresses concerns about the assumptions involved in the process.
  • Another participant explains that the comparison is made between carbon-14 and carbon-12, not nitrogen, and describes the use of mass spectrometry for this measurement.
  • It is noted that the ratio of carbon-14 to carbon-12 remains constant in living organisms but decreases after death, allowing for age estimation based on this ratio.
  • A participant raises questions about potential contamination from nitrogen in samples and whether it complicates age determination.
  • Concerns are expressed regarding the variability of nitrogen content in different samples and the implications for accuracy in measurements.
  • Some participants mention the historical decay of carbon-14 and the low decay rate, emphasizing that modern techniques do not rely on direct decay measurement.
  • There is a mention of the need for larger samples if decay measurements are to be taken directly, contrasting with mass spectrometry methods.

Areas of Agreement / Disagreement

Participants generally agree on the importance of comparing carbon-14 to carbon-12 rather than nitrogen, but there are differing views on the implications of contamination and the accuracy of measurements. The discussion remains unresolved regarding the best practices and assumptions involved in the dating process.

Contextual Notes

Participants highlight limitations related to sample contamination, the variability of carbon to nitrogen ratios, and the historical context of carbon-14 decay rates. These factors contribute to uncertainties in age determination.

UseAsDirected
Messages
34
Reaction score
0
Hello,

Are there any anthropologists, archaeologists, or geologists around on this board for help? I am trying to teach myself about radioactive decay via beta emission whereby a neutron spontaneously transmutes into a proton, releasing an electron. But, I do not understand the practical side. For instance, carbon-14 decays to become nitrogen on average about every 5,730 years. When an animal dies, its carbon-12 remains constant, carbon-14 decays to nitrogen. A scientist compares a sample of carbon-14 to nitrogen. I just can get the academic material -- if I had 14 grams of carbon-14 and 14 grams of nitrogen in an animal bone, I can guess that it started with 28 grams of carbon-14, 0 grams of nitrogen (a huge assumption). But, how does a scientist actually do this? How does a scientist get started? What exactly is done? I find an animal bone. What exactly do I do to find out how much material of carbon-14 there is and how much nitrogen there is, to compare? How does someone find out exactly how much of each there is? Creationists claim this first step is fraught with so many assumptions that the first step establishes a weak protocol.
 
Physics news on Phys.org
You don't compare carbon to nitrogen. You compare C-14 to C-12 by putting samples in a mass spectrometer.
The ratio of C-14 to C-12 is roughly constant in living material, but goes down after death with a known rate given by the lifetime.

To get a very naive and rough approximation (but more than sufficient to see that some samples are tens of thousands of years old), you can measure the C-14 to C-12 ratio of old samples and compare it to the ratio in living things directly after their death today: If you see half of today's ratio, the sample is roughly 6000 years old, if you see 1/4, the sample is roughly 12000 years old, and so on.

What is actually done is way more sophisticated, of course, to increase the accuracy. The C-14 to C-12 ratio in the biosphere varies a bit over time., so you need a track record of the ratio as function of time. Tree rings allow to measure that: take a tree that is 2000 years old (counted by rings) and still living. You can measure the C-14 to C-12 ratio in each ring and extrapolate it back to the time this ring was made. That improves the age determination for everything younger than 2000 years. Now consider a tree that lived e.g. from 1000 BC to 1000 AD: you know the C-14 to C-12 ratio for the second half of its life, so you can determine when the tree died with great accurary. The first 1000 rings then allow to determine the C-14 to C-12 ratio between 1000 BC and 0 AD. And so on. Some samples also have an age that can be determined independently via other methods.

And then you include all the other effects that have to be considered (also including those). And use all the other dating methods as cross-check. It is impossible to describe hundreds of pubications in a single forum post.

Ignore crackpots. It is just pointless to listen to them.
 
  • Like
Likes   Reactions: DelcrossA and Garlic
Thank you, that helps a lot. I am printing your response, and looking again at the Wikipedia summaries.

Now, why can't you compare carbon-14 to nitrogen? Is it because the sample can already have nitrogen in it, contaminating it, which invalidates the ability for it to be aged? Is it errant to claim that if I measure 10 grams of C-14 and 10 grams of N, then the sample started with 20 grams of C-14 and 0 grams of N and eventually will be 0 grams C-14 and 20 grams N? Is that mixed up logic?

Yes, the crackpots approach me already with their half-formed truths, only cite the evidence that backs up their opinion, ignore evidence, and ignore what I say. It is a waste of time, but I really need to understand this so that evidence can sway the 'borderline' people who are privy to both sides.

Thanks.
 
Every cell has nitrogen in it, mainly N-14. And you have to consider the scale: a sample that contains 10 g of N-14 has something like picograms (10-12 g) of C-14. The additional nitrogen from C-14 decays is completely negligible. You would have to know the initial N-14 to C-14 ratio very well, and you would get large uncertainties from that. To make it worse, the carbon to nitrogen ratio is different in every sample, even within the same species. You also have nitrogen gas in the atmosphere, and the amount that is dissolved is tricky to estimate.

C-14 to C-12 is much easier, as both carbon atoms have (nearly) identical chemical properties.
 
mfb said:
You don't compare carbon to nitrogen. You compare C-14 to C-12 by putting samples in a mass spectrometer.

One of the implications of this is that one does not measure the C-14 decay to measure the amount of C-14 (any more). It's the historic decay that matters.

The decay rate is very low - looks to be about 1 decay per four seconds per gram of modern carbon.
 
The decays can be measured, but that needs much larger samples than mass spectrometry.
 
That's why I said "any more".
 

Similar threads

  • · Replies 1 ·
Replies
1
Views
4K
  • · Replies 4 ·
Replies
4
Views
3K
  • · Replies 7 ·
Replies
7
Views
1K
  • · Replies 4 ·
Replies
4
Views
5K
  • · Replies 2 ·
Replies
2
Views
2K
  • · Replies 6 ·
Replies
6
Views
2K
  • · Replies 8 ·
Replies
8
Views
4K
  • · Replies 2 ·
Replies
2
Views
9K
  • · Replies 29 ·
Replies
29
Views
6K
  • · Replies 4 ·
Replies
4
Views
2K