About carbon isotopes and oxygen use…
1. The different carbon isotopes in nature.
The carbon of CO2 is composed of different isotopes. Most is of the lighter type: 12C, which has 6 protons and 6 neutrons in its nucleus. About 1.1% is the heavier 13C which has 6 protons and 7 neutrons in the nucleus. There also is a tiny amount of 14C which has 6 protons and 8 neutrons in the nucleus. 14C is continuously formed in the upper stratosphere from the collisions of nitrogen with cosmic rays particles. This type of carbon (also formed by above-ground atomic bomb experiments in the 1950’s) is radio-active and can be used to determine the age of fossils up to about 60,000 years.
One can measure the 13C/12C ratio and compare it to a standard. The standard was some type of carbonate rock, called Pee Dee Belemnite (PDB). When the standard rock was exhausted, this was replaced by a zero definition in a Vienna conference, therefore the new standard is called the VPDB (Vienna PDB). Every carbon containing part of any subject can be measured for its 13C/12C ratio. The comparison with the standard is expressed as d13C in per thousand (the term mostly used is per mil):
(13C/12C)sampled – (13C/12C)standard
————————————————————— x 1.000
(13C/12C)standard
Where the standard is defined as 0.0112372 part of 13C to 1 part of total carbon. Thus positive values have more 13C, negative values have less 13C. Now, the interesting point is that vegetation growth in general uses by preference 12C, thus if you measure d13C in vegetation, you will see that it has quite low d13C values. As fossil fuels were formed from vegetation (or methanogenic bacteria, with similar preferences), these have low d13C values too. Most other carbon sources (oceans, carbonate rock wearing, volcanic degassing,…) have higher d13C values. For a nice introduction of the isotope cycle in nature, see the web page of Anton Uriarte Cantolla ( http://homepage.mac.com/uriarte/carbon13.html ).
This is an interesting feature, as we can determine whether changes of CO2 levels in the atmosphere (observed to be currently -8 per mil VPDB) were caused by vegetation decay or fossil fuel burning (both about -24 per mil) or by ocean degassing (0 to +4 per mil).
2. Trends in carbon isotope ratios, the 13C/12C ratio.
From different CO2 baseline stations, we not only have CO2 measurements, but also d13C measurements. Although only over a period of about 25 years, the trend is clear and indicates an extra source of low d13C in the atmosphere.
Recent trends in d13C from direct measurements of ambient air at different baseline stations.
Data from http://cdiac.ornl.gov/trends/co2/contents.htm
ALT=Alert; BAR=Barrow; LJO=La Jolla; MLO=Mauna Loa; CUM=Cape Kumukahi; CHR=Christmas Island; SAM=Samoa; KER=Kermadec Island; NZD=New Zealand (Baring Head); SPO=South Pole.
Again, we see a lag in the trends with altitude and NH/SH border transfer and less variability in the SH. Again, this points to a source in the NH. If that is from vegetation decay (more present in the NH than in the SH) and/or from fossil fuel burning (90% in the NH) is solved in the investigation of Battle ea. http://www.sciencemag.org/cgi/reprint/287/5462/2467.pdf
More up-to-date (Bender e.a.) and not behind a paywall:
http://www.bowdoin.edu/~mbattle/papers_posters_and_talks/BenderGBC2005.pdf
Where it is shown that there is less oxygen used than can be calculated from fossil fuel burning. Vegetation thus produces O2, by incorporating more CO2 than is formed by decaying vegetation (which uses oxygen). This means that more 12C is incorporated, and thus more 13C is left behind in the atmosphere. Vegetation is thus a source of 13C and is not the cause of decreasing d13C ratios.
And we have several other, older measurements of d13C in the atmosphere: ice cores and firn (not completely closed air bubbles in the snow/ice). These align smoothly with the recent air measurements. There is a similar line of measurements from coralline sponges and sediments in the upper oceans. Coralline sponges grow in shallow waters and their skeleton is built from CO2 in the upper ocean waters, without altering the 13C/12C ratio in seawater at the time of building. The combination of atmospheric/firn/ice and ocean measurements gives a nice history of d13C changes over the past 600 years:
Figure from http://www.agu.org/pubs/crossref/2002/2001GC000264.shtml gives a comparison of upper ocean water and atmospheric d13C changes.
What we can see, is that the d13C levels as well as in the atmosphere as in the upper oceans start to decrease from 1850 on, that is at the start of the industrial revolution. In the 400 years before, there is only a small variation, probably caused by the temperature drop in the Little Ice Age.
In comparison, over the whole Holocene, the variation of d13C was only 0.4 per mil:
http://www.nature.com/nature/journal/v461/n7263/full/nature08393.html
And the change in d13C from the coldest part of the last glacial to the warm Holocene Optimum was only 0.7 per mil, slightly over the recent d13C change:
http://epic.awi.de/Publications/Khl2004e.pdf
The decrease of d13C in the atmosphere cannot be caused by some extra outgassing from the oceans, as that would INcrease the d13C ratios of the atmosphere (even including the fractionation at the ocean-air border), while we see a DEcrease both in the oceans and the atmosphere. This effectively excludes the oceans as the main cause of the increase.
3. The 14C/12C ratio
14C is a carbon isotope that is produced in the atmosphere by the impact of cosmic rays. It is an unstable (radioactive) isotope and breaks down with a half-life time of less than 6,000 years. 14C is used for radiocarbon dating of not too old fossils (maximum 60,000 years). The amount of 14C in the atmosphere is variable (depends of the sun’s activity), but despite that, it allows for a reasonable good dating method. Until humans started to burn fossil fuels…
The amounts of 14C in the atmosphere and in vegetation is more or less in equilibrium (as is the case for 13C: a slight depletion, due to 12C preference of the biological reactions). But about half of it returns to the atmosphere within a year, by the decay of leaves. Other parts need more time, but a lot goes back into the atmosphere within a few decades. For the oceans, the lag between 14C going into the oceans (at the North Atlantic sink place of the great conveyor belt) is 500-1500 years, which gives a slight depletion of 14C, together with some very old carbonate going into solution which is completely 14C depleted. In pre-industrial times, there was an equilibrium between cosmogenic 14C production and oceanic depletion.
Fossil fuels at the moment of formation (either wood for coal or plankton for oil) incorporated some 14C, but as these are millions of years old, there is virtually no 14C anymore left. Just as is the case for 13C, the amount of CO2 released from fossil fuel burning dilutes the 14C content of the atmosphere. This caused problems for carbon dating from about 1890 on. Therefore a correction table is used to correct samples after 1890.
In the 1950’s another human intervention caused trouble for carbon dating: nuclear bomb testing induced a lot of radiation, which nearly doubled the atmospheric 14C content. Since then, the amount is fast decreasing, as the oceans replace it with “normal” 14C levels. The half life time of the excess 14C caused by this refresh rate is about 5 years.
This adds to the evidence that fossil fuel burning is the main cause of the increase of CO2 in the atmosphere…
T4. Trends in oxygen use.
To burn fossil fuels, you need oxygen. As for every type of fuel the ratio of oxygen use to fuel use is known, it is possible to calculate the total amount of oxygen which is used by fossil fuel burning. At the other hand, the real amount of oxygen which is used can be measured in the atmosphere. This is quite a challenging problem, as the change in atmospheric O2 from year to year is quite low, compared to the total amount of O2 (a few ppmv in over 200,000 ppmv). Moreover, as good as for CO2 as for oxygen, there is the seasonal to year-by-year influence of vegetation growth and decay. Only since the 1990’s, oxygen measurements with sufficient resolution are available. These revealed that there was less oxygen used than was calculated from fossil fuel use. This points to vegetation growth as source of extra O2, thus vegetation is a sink of CO2, at least since 1990.
This effectively excludes vegetation as the main cause of the recent increase.
The combination of O2 and d13C measurements allowed Battle e.a. to calculate how much CO2 was absorbed by vegetation and how much by the oceans (see the references above). The trends of O2 and CO2 in the period 1990-2000 can be combined in this nice diagram:
O2-CO2 trends 1990-2000, figure from the IPCC TAR
http://www.grida.no/climate/IPCC_tar/wg1/pdf/TAR-03.PDF
This doesn’t directly prove that all the CO2 increase in the atmosphere is from fossil fuel burning, but as both the oceans and vegetation are not the cause, and even show a net uptake, and other sources are much slower and/or smaller (rock weathering, volcanic outgassing,…), there is only one fast possible source: fossil fuel burning.
Engelbeen on why he thinks the CO2 increase is man made (part 3)
About carbon isotopes and oxygen use…
-
The different carbon isotopes in nature.
The carbon of CO2 is composed of different isotopes. Most is of the lighter type: 12C, which has 6 protons and 6 neutrons in its nucleus. About 1.1% is the heavier 13C which has 6 protons and 7 neutrons in the nucleus. There also is a tiny amount of 14C which has 6 protons and 8 neutrons in the nucleus. 14C is continuously formed in the upper stratosphere from the collisions of nitrogen with cosmic rays particles. This type of carbon (also formed by above-ground atomic bomb experiments in the 1950’s) is radio-active and can be used to determine the age of fossils up to about 60,000 years.
One can measure the 13C/12C ratio and compare it to a standard. The standard was some type of carbonate rock, called Pee Dee Belemnite (PDB). When the standard rock was exhausted, this was replaced by a zero definition in a Vienna conference, therefore the new standard is called the VPDB (Vienna PDB). Every carbon containing part of any subject can be measured for its 13C/12C ratio. The comparison with the standard is expressed as d13C in per thousand (the term mostly used is per mil):
(13C/12C)sampled – (13C/12C)standard
————————————————————— x 1.000
(13C/12C)standard
Where the standard is defined as 0.0112372 part of 13C to 1 part of total carbon. Thus positive values have more 13C, negative values have less 13C. Now, the interesting point is that vegetation growth in general uses by preference 12C, thus if you measure d13C in vegetation, you will see that it has quite low d13C values. As fossil fuels were formed from vegetation (or methanogenic bacteria, with similar preferences), these have low d13C values too. Most other carbon sources (oceans, carbonate rock wearing, volcanic degassing,…) have higher d13C values. For a nice introduction of the isotope cycle in nature, see the web page of Anton Uriarte Cantolla ( http://homepage.mac.com/uriarte/carbon13.html ).
This is an interesting feature, as we can determine whether changes of CO2 levels in the atmosphere (observed to be currently -8 per mil VPDB) were caused by vegetation decay or fossil fuel burning (both about -24 per mil) or by ocean degassing (0 to +4 per mil).
-
Trends in carbon isotope ratios, the 13C/12C ratio.
From different CO2 baseline stations, we not only have CO2 measurements, but also d13C measurements. Although only over a period of about 25 years, the trend is clear and indicates an extra source of low d13C in the atmosphere.
Recent trends in d13C from direct measurements of ambient air at different baseline stations.
Data from http://cdiac.ornl.gov/trends/co2/contents.htm
ALT=Alert; BAR=Barrow; LJO=La Jolla; MLO=Mauna Loa; CUM=Cape Kumukahi; CHR=Christmas Island; SAM=Samoa; KER=Kermadec Island; NZD=New Zealand (Baring Head); SPO=South Pole.
Again, we see a lag in the trends with altitude and NH/SH border transfer and less variability in the SH. Again, this points to a source in the NH. If that is from vegetation decay (more present in the NH than in the SH) and/or from fossil fuel burning (90% in the NH) is solved in the investigation of Battle ea. http://www.sciencemag.org/cgi/reprint/287/5462/2467.pdf
More up-to-date (Bender e.a.) and not behind a paywall:
http://www.bowdoin.edu/~mbattle/papers_posters_and_talks/BenderGBC2005.pdf
Where it is shown that there is less oxygen used than can be calculated from fossil fuel burning. Vegetation thus produces O2, by incorporating more CO2 than is formed by decaying vegetation (which uses oxygen). This means that more 12C is incorporated, and thus more 13C is left behind in the atmosphere. Vegetation is thus a source of 13C and is not the cause of decreasing d13C ratios.
And we have several other, older measurements of d13C in the atmosphere: ice cores and firn (not completely closed air bubbles in the snow/ice). These align smoothly with the recent air measurements. There is a similar line of measurements from coralline sponges and sediments in the upper oceans. Coralline sponges grow in shallow waters and their skeleton is built from CO2 in the upper ocean waters, without altering the 13C/12C ratio in seawater at the time of building. The combination of atmospheric/firn/ice and ocean measurements gives a nice history of d13C changes over the past 600 years:
Figure from http://www.agu.org/pubs/crossref/2002/2001GC000264.shtml gives a comparison of upper ocean water and atmospheric d13C changes.
What we can see, is that the d13C levels as well as in the atmosphere as in the upper oceans start to decrease from 1850 on, that is at the start of the industrial revolution. In the 400 years before, there is only a small variation, probably caused by the temperature drop in the Little Ice Age.
In comparison, over the whole Holocene, the variation of d13C was only 0.4 per mil:
http://www.nature.com/nature/journal/v461/n7263/full/nature08393.html
And the change in d13C from the coldest part of the last glacial to the warm Holocene Optimum was only 0.7 per mil, slightly over the recent d13C change:
http://epic.awi.de/Publications/Khl2004e.pdf
The decrease of d13C in the atmosphere cannot be caused by some extra outgassing from the oceans, as that would INcrease the d13C ratios of the atmosphere (even including the fractionation at the ocean-air border), while we see a DEcrease both in the oceans and the atmosphere. This effectively excludes the oceans as the main cause of the increase.
-
The 14C/12C ratio
14C is a carbon isotope that is produced in the atmosphere by the impact of cosmic rays. It is an unstable (radioactive) isotope and breaks down with a half-life time of less than 6,000 years. 14C is used for radiocarbon dating of not too old fossils (maximum 60,000 years). The amount of 14C in the atmosphere is variable (depends of the sun’s activity), but despite that, it allows for a reasonable good dating method. Until humans started to burn fossil fuels…
The amounts of 14C in the atmosphere and in vegetation is more or less in equilibrium (as is the case for 13C: a slight depletion, due to 12C preference of the biological reactions). But about half of it returns to the atmosphere within a year, by the decay of leaves. Other parts need more time, but a lot goes back into the atmosphere within a few decades. For the oceans, the lag between 14C going into the oceans (at the North Atlantic sink place of the great conveyor belt) is 500-1500 years, which gives a slight depletion of 14C, together with some very old carbonate going into solution which is completely 14C depleted. In pre-industrial times, there was an equilibrium between cosmogenic 14C production and oceanic depletion.
Fossil fuels at the moment of formation (either wood for coal or plankton for oil) incorporated some 14C, but as these are millions of years old, there is virtually no 14C anymore left. Just as is the case for 13C, the amount of CO2 released from fossil fuel burning dilutes the 14C content of the atmosphere. This caused problems for carbon dating from about 1890 on. Therefore a correction table is used to correct samples after 1890.
In the 1950’s another human intervention caused trouble for carbon dating: nuclear bomb testing induced a lot of radiation, which nearly doubled the atmospheric 14C content. Since then, the amount is fast decreasing, as the oceans replace it with “normal” 14C levels. The half life time of the excess 14C caused by this refresh rate is about 5 years.
This adds to the evidence that fossil fuel burning is the main cause of the increase of CO2 in the atmosphere…
4
-
Trends in oxygen use.
To burn fossil fuels, you need oxygen. As for every type of fuel the ratio of oxygen use to fuel use is known, it is possible to calculate the total amount of oxygen which is used by fossil fuel burning. At the other hand, the real amount of oxygen which is used can be measured in the atmosphere. This is quite a challenging problem, as the change in atmospheric O2 from year to year is quite low, compared to the total amount of O2 (a few ppmv in over 200,000 ppmv). Moreover, as good as for CO2 as for oxygen, there is the seasonal to year-by-year influence of vegetation growth and decay. Only since the 1990’s, oxygen measurements with sufficient resolution are available. These revealed that there was less oxygen used than was calculated from fossil fuel use. This points to vegetation growth as source of extra O2, thus vegetation is a sink of CO2, at least since 1990.
This effectively excludes vegetation as the main cause of the recent increase.
The combination of O2 and d13C measurements allowed Battle e.a. to calculate how much CO2 was absorbed by vegetation and how much by the oceans (see the references above). The trends of O2 and CO2 in the period 1990-2000 can be combined in this nice diagram:
O2-CO2 trends 1990-2000, figure from the IPCC TAR
http://www.grida.no/climate/IPCC_tar/wg1/pdf/TAR-03.PDF
This doesn’t directly prove that all the CO2 increase in the atmosphere is from fossil fuel burning, but as both the oceans and vegetation are not the cause, and even show a net uptake, and other sources are much slower and/or smaller (rock weathering, volcanic outgassing,…), there is only one fast possible source: fossil fuel burning.
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This is a great article.
What he points out that many source of CO2 that many skeptics have cited are in fact invalid. So yes there is a large source of CO2 undetermined. Given that humans have been generating CO2 in an exponential amount since the 1800’s, this does seem like an obvious choice. Yet many say SHOW ME THE MONEY. I say ok, fine, show me your theory about what ELSE is causing CO2 increase, if not humans?
Here is the graph of CO2 increase compared to population increase over the same time period. Increased use of fossil fuels does not show the same hockey stick shape and I can’t find a 2000 year graph.
http://www.niwa.co.nz/our-science/climate/information-and-resources/clivar/gases
http://www.theoildrum.com/story/2005/12/18/1387/0641
What I am trying to find is a rather regular (almost mathematically regular) source of increasing CO2 that would lead to the stair stepping CO2 graph. Population increase is now so large that it is developing an exponential (almost mathematically regular) shape. Since population increase and CO2 increase do not match energy consumption increase over the same period (and I wish I had a good graph of energy consumption over this time period), especially in China and India, I just have to wonder if the immediate increase is from breathing out. If someone can find a graph of world energy consumption over the last 2000 years (and of course this has to be modeled), please post. I could be barking up the wrong tree ring here. Remember that back in the day, open fires, inside or outside, were very inefficient ways of keeping a house warm or cooking a meal, so EVERY household burned lots and lots of energy on a daily basis. Energy use now is WAY more efficient than it used to be. This could be why the graphs I have seen so far are really messy and don’t agree with each other at all.
Ferdinand,
1. The carbon deposits to call “fossil fuels” are not derived from recycled biomass or fossils – unless the laws of thermodynamics have changed.
2. The Carbon isotope ratios cannot discern biogenic from non biogenic sources, especially when an archaen diamond has “observation by Giardini & Melton6 that such cannot be considered a reliable criterion for ascertaining the origin of petroleum. Giardini & Melton took a primoridial natural diamond of 8.65 carats and measured the carbon isotope ratio of the CO2 entrapped in its inclusions. The results were an isotope ratio of –35.2% on the standard PeeDee scale. Previously the carbon isotope ratios more negative than – 18.0% had been assigned a biological origin. The diamond tested by Giardini & Melton was measured to be of an age of crystallization of at least 3.1 x 10^9 years, well before any record of biological life on Earth. The observation by Giardini & Melton destroyed any claimed validity of the carbon isotope ratio as a determinant of the origin of petroleum, – and probably of any other carbon compound.”
There is an outstanding prize of US$10,000 for anyone who can demonstrate empirically and experimentally that petroleum can spontaneously form from subjecting biomass to the pressures and temperatures typical for the bottom of sedimentary basins.
However, experimental evidence of the spontaneous production of hydrocarbons from a mixture of CaCO3, FeO and H20 has been published and replicated. The fossil fuelers, however, continue their assertions by resort to rhetoric or applying the logical fallacy of arguing the consequent.
QED.
Smokey
“There is nothing unusual about the current rise in temperatures. They have been exceeded many times during the Holocene, although much colder temperatures are the norm.”
there is nothing “unusual” about the fall in temps after a volcanp. nevertheless we can explain that variation by understanding the physics. The increase in temps may well be within the entire envelop of past changes. That says Nothing about the cause of the current rise and nothing about the rate of increase. But for the addition of C02 since say 1850 it would be cooler than it is now.
Think of it this way. You watch a car decelerate from 60 miles per hour to 0.
and another. and another. and still more. and you conclude from this that it is natural for a car to decelerate to 0. Now did they decelerate because
1. the driver took the pedal off the gas
2. the car ran out of gas
3. it hit the wall
4. the driver hit the brakes.
On your view of things they all did the same thing so there is nothing unusual about a car slowing. the case for AGW is not made on the usualness or unusualness of the magnitude of the rise. It made from observing that physics predicts that if you put more C02 in the atmosphere temperatures will go up. Similarly, I could predict that if you apply the brakes the car will slow down. Its not a counter argument for you to point out that other things can slow a car down, or that some cars in the past slowed down because they hit walls or ran out of gas, or ran out if gas while the brakes were being applied. GHGs warm the planet. More GHGs make matters worse. are their other factors? of course. Do GHGs DOMINATE the change? that is the real question.
Jean Parisot says:
September 16, 2010 at 7:17 pm
How is the uneven distribution of atmospheric CO2 factored into various IPCC models?
It isn’t. The models assume that the atmospheric gases are “well-mixed” and that distribution of mass is uniform, but they do take into account that the density of the
atmosphere decreases with altitude
As I mentioned above, high pressure cells have more mass than low pressure cells.
Water vapor lowers the density of air and there is no uniforn distribution of it in the lower atmosphere, i.e. below 30,000 ft.
The water droplets of clouds contain atmospheric gases including CO2 and the clouds can transport these gases to various locations. The amount of CO2 held in clouds would be difficult to estimate but it is not zero. Rain can “wash” CO2 out of the atmosphere.
Ferdinand,
Thanks for the article, however Dave Springer’s methane arguments are valid and need to be considered further. Regrettably fossil fuels are not the only potential reservoir of light carbon that can exchange with atmospheric CO2. Your arguments are sound and there probably is a component of fossil light-carbon in the lowering of the delta C13 ratios of atmospheric CO2, it is just that without knowing the methane contribution you can not prove your case.
John Whitman:
“Steven Mosher,
“I think your statement is not quite right. It appears to be that you are claiming that GHGs (all of them) combined with all other known and unknown processes involved in the earth system warm the planet. I do not think this has ever been demonstrated scientifically. By themselves in a simplified (non-realistic) scenarios without the total earth system processes included there have been discussions about possibility of GHGs warming the planet, maybe that is what you are thinking . . . . but they are just discussions. Your claim is often assumed / postulated /implied / believed . . . . . all those yes but demonstrated scientifically . . . no. If you can show it scientifically or cite papers that show it then please do so for everyone’s benefit. Then we will provide falsifications. Until then there is nothing for us to falsify.”
1. we know from physics that GHGs warm the planet.
2. There is no physical theory to even suggest that they cool the planet
3. The question is, how much
A. so small as to be non measureable
B. large enough to be measurable
Further, like many people you utterly misunderstand the the notion of “falsification.” no theory is falsified. Theories have to be “falsifiable.” That speaks only to this: they have to make statements that can be measured against observations. So simply the theory that holds that increasing GHGs will warm the planet is confirmed ( never proven) by our observations. Since 1850 ghgs have increased, so has the temperature. Further, if we try to predict the course of temperature from 1850 to today and hypothecate no forcing from C02 our predictions go horribly wrong. (see ch09 ar4) Absent any evidence or theory that GHGs cool the planet, and in light of theory and evidence that consistently claims they will, the balance of the evidence warrants the rational belief that they do. Theory predicts they will. they have.
“By just looking at the climate data (temps) there is nothing in it that proves GHGs warm the planet. It needs a theory to be developed and be stated as a hypothesis and be tested against the climate data.”
The theory that GHGs (like water vapor) warm the planet is well established and well developed. It’s been stated as a hypothesis for over a hundred years. the data confirms the theory. no theory is EVER proven. ever. We only have degrees of certitude. Is it logically possible that GHGs could not cause warming? sure. Is there any theory that suggest this? no. if there WAS, then that theory would be at odds with the last 160 years of data.
“As for natural variability, prior to man’s hypothesized influence , the climate sure did vary widely. The data shows that. No need for a theory and hypothesis to see that climate varied significantly before man’s influence . . . just look at the data. It had to be natural, no man influence. A hypothesis is only needed if you wish to understand why it varied and what natural variability consists of by mechanisms.”
i’m far more skeptical of data before 1900 than any of the so called skeptics here. nevertheless, as you point out, merely pointing to variability is no theory. For the incurious, I suppose one could observe that people get old and die. its natural. for the scientist, for the curious, its human nature to wonder why and to try to explain it. So, merely pointing at variability and grunting “nature” is not very interesting in my book but it seems to be enough for some folks. go figure.
John
Thanks all for the lot of comments!
As I am travelling now with limited Internet access, my reactions on the main points will be for tonight…
Ferdinand
intrepid_wanders says:
While I do understand the hypothesis that is being presented, there still remains the issue of “understanding” of isotopes specifically, carbon.
C-12 -> Stable
C-13 -> Stable
C-14 -> beta decay + N14
N-14 + n -> C-14 + H-1
B-13 -> C-13 + beta decay
So, the first thing that comes to mind is the source of C-13 is B-13 with an electron ejection (decay is tens of millisecs).
You’d also need something producing the boron 13 to decay to carbon 13. This production of carbon 13 would appear to be more likely to happen in stars than on the surface of Earth.
Conversion of nitrogen to carbon happens in the upper atmosphere, which is mostly nitrogen anyway. However carbon 14 has been found in fossil fuels. Coal is mostly carbon, oil is mostly carbon and hydrogen. So it appears that other nuclear reactions an create this isotope of carbon. If this is neutron capture such coal or oil may well contain more heavy carbon (and hydrogen) isotopes. But that not exposed to a source of neutrons would contain carbon from the original organic sources. These sources likely to be random and variable anyway.
@WSBRIGGS
http://chiefio.wordpress.com/2009/02/25/the-trouble-with-c12-c13-ratios/
Harvey says:
quote
I say ok, fine, show me your theory about what ELSE is causing CO2 increase, if not humans?
unquote
Reduced pull-down into deep ocean rather than increased output by humans. Pulldown mechanism tending towards heavier isotopes as diatoms and C4 phytoplankton take more of the load. You can find a recent report of phytoplankton population decline by Googling “Global phytoplankton decline over the past century
Daniel G. Boyce1, Marlon R. Lewis2 & Boris Worm1” and a general search will show you the carbon metabolic response of starved phytoplankton. The effects of human-induced dust increases can be found by searching for “Increasing eolian dust deposition in the western United States linked to human activity”, and further searches on the limitation of diatom populations by silica availability is easily done. From this information you may easily show that a) starved phytoplankton will pull down relatively more 13C and 14C b) diatom populations will increase relative to the calcareous phytos in an ocean which is being fed with more silica c) diatoms pull down more heavy isotopes of carbon compared to well-fed calcareous phytos.
Or:
Minute warming of deep ocean methane deposits by currents responding to the MWP. Increased metabolic activity by methanophages in response, emitting light isotope CO2. See graphs of warming followed by CO2 increase in many articles about historical CO2 levels, with the lag being hundreds of years.
Or:
Methane deposits in polar regions responding to reduced acid rain levels as pollution controls reduce sulphate emissions. More light signal methane emitted and metabolised by bacteria.
Or:
Oil and surfactant pollution of ocean surface means fewer breaking waves, less efficient entrainment of CO2 by bubbles and reduced dissolving of CO2. (Note that matches of ocean and atmosphere CO2 levels have been done in shallow water where mixing by wave action is assured.)
Or:
something we haven’t thought about.
Steven Mosher: you pride yourself on your rigorous take on the science, excoriating (rightly in my view but what do I know?) those who try to reject basic scientific facts like the greenhouse effect. Can I ask you to do something for me? Examine the graph above, (Fig 4, the sponge isotope data) and simply post here the dates at which you see the light isotope signal beginning. Three dates, of course, Jamaica, Pedro Bank and atmospheric.
Do any of your dates match Ferdinand’s assertion that :
quote
What we can see, is that the d13C levels as well as in the atmosphere as in the upper oceans ***start to decrease*** from 1850 on, that is at the start of the industrial revolution. In the 400 years before, there is only a small variation, probably caused by the temperature drop in the Little Ice Age.
unquote
TIA
JF
*** my emphasis
Our input of CO2 from burning fossil fuels is 3% of the total annual input. the rest is from natural sources. ( these figures are from the US Dept of Energy who I assume have done their homework). So there is no way that all the current increase are our fault. We must also look at the residence time of CO2 in the atmosphere and if we believe the IPCC this is 200 years. If we believe current research it is 3-5 years possibly less. Ice core research also shows that temperature increase is followed by a parallel increase in atmospheric CO2 600 to 1000 years later. So today’s modest increase is caused by the Medieval Warm period not use of coal.
All this isotope research is based on several assumptions. One I find strange is the carbonate content at 1% in the graphic above. Considering that limastone is the ost prolific of sedimentary rocks and aged back to pre-cambrian times I think that this assumption is very wrong.
Steven mosher says:
September 16, 2010 at 10:40 pm
1. we know from physics that GHGs warm the planet.
2. There is no physical theory to even suggest that they cool the planet
3. The question is, how much
Wrong, wrong and wrong again!
http://www.spinonthat.com/CO2_files/The_Diurnal_Bulge_and_the_Fallacies_of_the_Greenhouse_Effect.html
Ben M says
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Isn’t this much the same as the warmists when they say “we don’t know what else could have caused the rise in temperatures since 1975, therefore it must have been human-emitted CO2″?
The argument from ignorance is only evidence of our ignorance.
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Ben it’s just an simple accounting problem.
If the book-keeper finds a big hole in the balance sheet you go looking for the embezzler.
You don’t expect that the money just evaporated into thin air.
mkelly says:
September 16, 2010 at 6:43 am
More molecules of water are added to atmosphere by at least 2:1 and reducing O2.
So if you are looking to prove AGW it would be sensible to monitor and track the levels of oxygen, carbon dioxide and water vapour in the atmosphere… simples… atmospheric changes would reflect the chemistry of burning fossils… simples… but no… the AGW argument seems to rest upon dubious measurements and proxies of unknown validity… I just don’t get it… more to the point: I just don’t buy it… and if the AGW theory was right then the real story would be about declining oxygen levels… so again I just don’t get it and I just won’t but it.
The oceans are massive temperature sensitive depositories of CO2… they absorb CO2 when they cool… and outgas CO2 when they warm… if the earth is warming then we should expect atmospheric CO2 levels to rise… and looking at the official data this is exactly what is happening… no surprise.. no problem.. and even if you think it is a problem (which is very unfortunately for you) it is a problem you can’t resolve because mankind is just too insignificant… as King Canute proved many centuries ago – man can’t command the tide. Now I have a lot of respect for King Canute… he didn’t use the tides – not a proxy for tides… he used actual observations – he didn’t fiddle with the high and low water mark readings… if only the AGWers had the same integrity as King Canute.
The more AGW tracts I read the more convinced I am that we are dealing with missionaries from the Victoria age… in those days white men wearing dog collars would sail away to some far flung continent and start talking to the indigenous heathens… there they would try to terrorise the uneducated locals with stories of a fiery hell and eternal damnation… and if they still didn’t convert then they would buy off the chief with some western trinkets.
In this day and age the AGW missionaries believe in their moral and intellectual superiority… they cloak themselves in the white coat of the scientist… and then they set sail to talk to the sheeple… again they try to terrorise the sheeple with their stories of how the earth is being turned into a fiery hell… and again if that doesn’t convert the indigenous heathens they start buying off leaders with money so the leaders can buy more western trinkets.
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Steven Mosher,
Thank you for your thoughtful reply.
We are not discussing this topic on a shared set of fundamental ideas. Namely, we do not share the same set of fundamental ideas on what is the basis of human knowledge and therefore scientific knowledge. That is common among individuals. I think discussion of those fundamental ideas, which we do not share, will take us far off topic on this post.
We agree to disagree. Nature will decide for us.
John
Ferdinand,
If it is possible to measure the changes in the amount of CO2 in the atmosphere to better than 0.1 ppm, why is it not possible to do the same for O2?
Roll up! Roll up!
Lets plays Pin the Tail on the Mauna Loa Donkey
Background
========
1) Study the global CO2 level map produced by NASA – shown at the top of this page.
2) Study the latest CO2 readings from Mauna Loa – see http://en.wikipedia.org/wiki/File:Mauna_Loa_Carbon_Dioxide-en.svg
Technique
========
Locate Mauna Loa on the CO2 map by matching up the CO2 levels.
Winning The Game
==============
Winning the game requires you to have correctly identified the geographic location of Mauna Loa on the CO2 map.
WARNING
========
Do not use a pin to locate Mauna Loa on your computer screen… a clean finger is recommended.
LEGAL
=====
The organisers of this competition reserve the right to alter the data and the map of the globe at any time.
Louis Hissink,
“However, experimental evidence of the spontaneous production of hydrocarbons from a mixture of CaCO3, FeO and H20 has been published and replicated.”
While the abiogenic hypothesis is an intriguing one, and chemically plausible, opponents do have one serious criticism. That is, at the high temperatures associated with this inorganic reaction, the hydrocarbons rapidly breakdown. If true, I would say this is a serious problem.
Tips on how to win Pin the Tail on the Mauna Loa Donkey
1) Remember the NASA map is for July 2003
2) Remember the NASA map is for the atmosphere at an altitude of 8 kilometres
3) Remember the Mauna Loa observatory is at an altitude of 3397 metres
4) Remember that CO2 levels change with altitude – see http://www.biomind.de/realCO2/realCO2-1.htm
Steven mosher,
“Similarly, I could predict that if you apply the brakes the car will slow down. Its not a counter argument for you to point out that other things can slow a car down, or that some cars in the past slowed down because they hit walls or ran out of gas, or ran out if gas while the brakes were being applied. GHGs warm the planet.”
Clever, but false analogy. We know that the car will slow down and stop if you apply the brakes. We don’t know that adding more CO2 will warm the planet at all because we don’t know the sign and magnitude of the feedbacks.
Pursuing your car analogy, we should envisage a car where the hydraulic cable feeding the brakes have holes, and the brake is connected to the throttle by some complex serious of interconnections, the aggregate result of which is unknown, and the driver is sitting on a chair affixed to the roof of the car and attempting to press the brake peddle with the handle of a broom (the last part thanks to Mr Bean).
That is the true CO2 analogy.
nvw says:
September 16, 2010 at 10:23 pm
Thanks for noticing. It can be very frustrating when you know you have a valid point and no one takes note of it. Englebeen clearly needs to address it but he can dodge it, purposely or otherwise without appearing dishonest, when it is buried amongst a large number of unrelated comments begging a response.
Dave Springer says:
September 17, 2010 at 5:56 am
when you know you have a valid … but he can dodge it….
Without a doubt anything can be dodged in the land of smoke and mirrors.
@nvw
P.S. One can never prove an argument from ignorance. That doesn’t make them invalid scientific hypotheses however. Karl Popper explained how to make an argument from ignorance a valid scientific hypothesis with his well known example of white swans. Popper formed the hypothesis that “all swans are white”. At the time a colored swan had never been observed. He pointed out that it would be impossible to prove that are no colored swans in nature because there was no known scientific principle that forbids a colored swan and no matter how thorough the search for a colored swan the possibility would always remain that somewhere a colored swan was overlooked. He then went on to describe falsification. The hypothesis that no colored swans exist in nature could be disproven by the discovery of a single colored swan. Thus the hypothesis was legitimate and following from that any similar argument from ignorance in science is legitimate so long as it can, at least in principle, be disproven.
Englebeen made a legitimate colored swan argument. He hypothesized that nothing exists in nature that can duplicate the fossil fuel light carbon isotope signature. I disproved his hypothesis by showing that methane can produce the same signature. Methane, in this case, is equivalent to finding a colored swan.
Just for a historical note of reference the Australian Black Swan was discovered subsequent to Popper’s example of falsification.
More on Popper and falsification here:
http://en.wikipedia.org/wiki/Falsifiability#Two_types_of_statements:_observational_and_categorical