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.





Why would anyone in their right mind WANT to “cause a net decrease in CO2” and risk the extinction of photosynthetic plant life?
Increased plant growth encourages a greater mass of plant life to grow in previously marginal terrestrial and marine environments. The increased mass of plant life consumes more CO2. The increased rate of CO2 consumption maintains the CO2 concentrations at whatever minimum level the Plant Kingdom can no longer diminish. In the event of a sudden change of climate from a warmer inter-glacial period to a colder ice age, the disruption of the carbon cycle for plant life could result in =<~180ppm levels too low for photosynthesis and too fast for adaptation to avoid extinction.
Burning fossil fuels may or may not result in lower CO2 concentrations in the atmosphere, but it is not inconceivable for fossil fuels to stimulate enough new plant growth to generally maintain concentrations or lower them in some other circumstances.
Incorrect, you cannot distinguish carbon with the ratio from what comes out of volcanoes
http://carbon-budget.geologist-1011.net/
3.0 Abusing Doctor Suess: Pulling the Cat out of the Hat
So far, the evidence presents the rather tantalizing implication that volcanogenic CO2 emission is a significant if not dominant contributor to atmospheric CO2 levels. The next logical step for those trying to prove that the CO2 rise is anthropogenic is to find a signature to fingerprint anthropogenic CO2 as separate from all other sources of CO2. The research of one Harmon Craig, first submitted for publication on ISO:1953-Apr-20, found that 13C & 14C are enriched in carbonates. Harmon Craig discusses the carbon dating errors that can be introduced by natural isotopic fractionation, along with other processes (Craig, 1954). While Rankama (1954), suggests that 13C depletion is characteristic of biogenic sources, Craig (1954) goes so far as to suggest the use of 13C as a tracer for 14C. This becomes the subject of research by Hans E. Suess into the contamination of 14C dates by variations in normal atmospheric 14C, which quantified the effect of processes discussed by Craig (1954). Part of Suess’ explanation of his own results was seized upon as a way to fingerprint fossil fuel CO2 because fossil fuels, being too old to contain measurable amounts of this cosmogenic isotope, will deplete atmospheric concentrations of 14C when burned. In Cleveland & Morris (2006, p. 427) Hans Suess and the Suess Effect, used to account for contamination of radiocarbon dates by various phenomena, are given the following entries:
Suess, Hans 1909-1993, U.S Chemist who developed an improved method of carbon-14 dating and used it to document that the burning of fossil fuels had a profound influence on the earth’s stocks and flows of carbon. (Fossil fuels are so ancient that they contain no C-14.)
………
Source : http://carbon-budget.geologist-1011.net/
REPLY: SNIPPED MAJORITY OF CONTENT – please don’t repost entire website stories here. That’s what links are for – Anthony
Methane forcing is about 20% of all GHG forcings. It has increased from about 700 to 1800 parts per billion in the last century or 4 times faster than CO2. Interestingly it decays into CO2 after ten years. So that means it has added CO2 to the atmosphere over the past century about 18000 parts per billion or 18 parts per million. This then accounts for over 20% of the increase in CO2 since pre-industrial times (87ppm).
You can check the numbers above here:
http://en.wikipedia.org/wiki/Greenhouse_gas#Greenhouse_gas_emissions
If CO2 from degradation of methane was exactly as light in heavy carbon isotopes as carbon from coal and oil then it would account for 20% of the isotope “signature” i.e. the slightly declining heavy carbon isotopes over the past century as graphed in the OP.
But wait, I also provided links in previous comments establishing the fact that CH4 is twice as light in heavy carbon isotopes as fossil fuel carbon. So it has twice the diluting effect or about 40% of the so-called fossil fuel isotope signature.
This of course raises the question of how much methane is anthropogenic and/or what the heck is driving its rapid increase in the past century. If the increase is either anthropogenic and/or a natural source that can be reduced then, given its residence time in the atmosphere is only 10 years, it appears to be much lower hanging fruit if one’s interest is truly in reducing the ostensibly growing and eventually catastrophic greenhouse effect. If we could bring methane emissions back to pre-industrial level it would reduce anthropogenic global warming by more than ten percent in ten years. There is no way to get such a fast reduction in greenhouse warming by actions taken to reduce CO2 emissions.
R. Gates says: “…Only an extreme minority currently would ever seriously no doubt that human activity has caused the 40% increase in CO2 since the 1700′s.”
Yes, R, we know you think science is about taking a vote.
“So while this is an interesting, and mostly accurate post, it is hardly earth-shattering or particularily interesting.”
Uh, so it’s interesting but not particularily [sic] interesting. Right.
“The core issue really is how sensitive is the climate system to this anthropogenic based increase in CO2. And of course the next step that some are working on already is some sort of geoengineering efforts to reduce the CO2 levels or mitigate their effects.”
And those efforts, being based on ‘consensus’ drivel instead of science, will fail.
Scarlet Pumpernickel says:
September 16, 2010 at 4:09 pm
Yes but is there any reason to believe that volcanic activity increased at the same time the industrial revolution began? If not then it’s a constant factor that can be ignored unlike, say, planetary albedo which is modeled as a constant but is actually known to be a significant variable with very poor understanding of what causes the variation.
D. Patterson:
“Burning fossil fuels may or may not result in lower CO2 concentrations in the atmosphere, but it is not inconceivable for fossil fuels to stimulate enough new plant growth to generally maintain concentrations or lower them in some other circumstances.”
You missed the point. Absent any evidence that burning Fossil fuels causes a net decrease, absent ANY argument, I think the reasonable alternative is the obvious.
It causes a net increase. Now that obvious conclusion also happens to be supported by a wealth of evidence which our kind author has assembled over three posts. There is no evidence of a net decrease from burning FF, there is substantial ( but never conclusive) evidence that it causes a net increase. The possibility that you might doubt it, does not amount to an argument. So, I am waiting for someone to argue that it causes a decrease, and back that argument up.
Nick Stokes says:
quote
This is an excellent article, which sets out the facts systematically, and makes it easy to understand. Congratulations, Ferdinand.
unquote
Nick, forget the money from sweet Solitaire (I assume you are paid by that pert Poictesme* of an old man’s dreams, because I can imagine no other reason for your blindness) and look at the second graph above.
Ferdinand says that it’s obvious that the change began in 1850. Que? Look carefully. When does the ratio begin to change? Come on, look. Does it really only begin to go down in 1850? If you believe that you need a) an eye test and b) a brain transplant. This is science as delusion, when even a graph which refutes the hypothesis is offered as proof of it.
From the main post:
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.
unquote
Ferdinand, that is utter tosh. Look at the graph. When does the ratio of 13C/12C start to decrease? Look, please trust your eyes. No, there is no sudden change in 1850. It starts to go down in 1700 (ish). OK, the fall increases in 1850, but it doesn’t start then. Why, my dear chap, does it fall from 1700 to 1850? If you’d like an explanation I’ll do it tomorrow (a hard folkie night tonight with added whisky, but look up diatoms, and silica as a critical resource for these pretty members of the plankton population) and in the meantime please look at that graph and ask yourself how you have got to a state where you can choose 1850 as a significant date.
Interesting that you have made the same error here as you did with the CO2 mass balance — you are confusing an increase in production with a reduction in sink.
JF
*pronounced ‘pwah-temm’, an earthly paradise, an unattainable summit of earthly desire. Aka ‘a yummy mummy’. [waves]
Charles S. Opalek, PE says:
September 16, 2010 at 4:07 pm
The problem is nature is evidently only sequestering 98.5% the total emissions each year and the remainder is accumulating as a rising atmospheric CO2 concentration. One of the least contestable facts in this matter is that atmospheric CO2 levels have began rising faster and faster since the beginning of the industrial revolution where human activity emits twice the amount it takes to account for the rise.
That in itself is very interesting as it raises the question of what’s happening in nature that is sequestering half of human emissions. Someone else mentioned in this thread, and I’ve brought up the point myself in other threads, that the ocean determines the equilibrium point of atmospheric CO2 and that if human contribution is absent the ocean would have outgassed more of its vast store (many times greater than the atmosphere) of CO2 and the current level would still be 380ppm and rising. The most likely suspect for a change in oceanic equilibrium point is that the Little Ice Age ended about the same time the industrial revolution started and the ocean’s delayed response to the end of several centuries of ice-age cold is raising the partial pressure equlibrium point of the ocean/atmosphere interface. This greater equilibrium point could be satisfied by either human contribution directly to the atmosphere or in the absence of human emission the ocean would have released the same amount.
I’m not saying that the ocean determines the partial pressure equilibrium point of atmospheric CO2 but it very well could and that must be falsified in some manner before we can know that any reduction in human emissions will actually reduce CO2 partial pressure. For all we know we could reduce anthropogenic emissions and the ocean, still seeking the same equilibrium point, would just replace the human emission with oceanic emission.
Vince Causey – you are using an equation that gives the globally averaged forcing from a change in the global average CO2 concentration. Regional variations can’t, I don’t think, be evaluated in the same way.
Smokey: calculations by many groups of scientists have shown that natural variations cannot be the cause of the current warming. Roy Spencer must, I think, have his own idiosyncratic definition of “falsified”.
ATTN: Pamela Grey
The short answer is no. In a chemical reaction, molecules containing C-13 react slightly slower than molecules containing C-12. This is called the kinetic isotope effect and is temperature dependent. However, the difference in reaction rates depends on the formula weight of the molecules in some reaction. Carbon dioxide containing C-12 has a formula weight of 44 vs 45 for molecules containing C-13 which would react about 2% slower and have a slightly lower rate of diffusion into plant leaves for example.
BTW, the concentration of CO2 in a local sample of air is reported for purified dry air which does not occur in the earth’s atmosphere and is comprised of nitrogen, oxygen and the inert gases, which are the fixed gases, and CO2. Climates models are fatally flawed because (1) these use the wrong metric for CO2 and (2) there is no uniform distribution of the masses of various constituents of the atmosphere in space and time as shown by daily weather maps. High pressure cells have more mass than do low pressure cells. More importantly there is no uniform distribution of water as vapor and clouds
Note, too, that there are natural seeps of methane (and other stuff). Methane is currently being recovered from one such seep in California. Most seeps just bubble up into the atmosphere and probably have been doing so for a long, long, long time.
http://www.countyofsb.org/energy/information/seepspaper.asp#naturalSeeps
So explain it to me again. The ratio between lighter and heavier CO2 is getting smaller. And the overall CO2 amount in the air is increasing. So we are putting more of the lighter isotope CO2 into the air because of fossil fuel, animal life, and decaying vegetation emits this isotope thus decreasing the ratio of lighter to heavier CO2. If what we breath out has 4 times more CO2 than what we breath in, with an average -0.5 ratio in human breath, with population growth of 6 billion since the start of the industrial age, and growing exponentially, wouldn’t that affect the ratio as well? If you say plants are using it, fine, but we still keep pumping out more CO2 than we breath in. And we are doing it in exponentially greater amounts.
So who has the calculation? I’ve included a graph and reference to population growth. It has quite a hockey stick shape to it. Looks a lot like the growth in CO2. I wonder where the population explosion is taking place? In countries with a car in every driveway? Hardly.
http://www.theoildrum.com/story/2005/12/18/1387/0641
I am not stuck on this but I fail to see the closed system here regarding human breath if what we are talking about is the increasing measurement of CO2 in the air and asking where the CO2 increase is coming from. It has to be readily available and robust to downturns in fossil fuel burning.
It just seems to me that the population boom might match CO2 growth much better than standard of living growth for those countries involved in the explosion (which by definition includes having energy to make your new cars and gadgets go).
At one time, I was intrigued with the idea that the modern CO2 increase might be a result rather than a cause of the modern temperature increase, however the extreme sensitivity required to make this work when average global temperatures have only changed 0.6 to 0.7 degrees C on a base level of 14 degrees C since 1880 (I suspect many people probably believe this must have been at least a 3 degree C change to justify all the hype and alarm) means that the CO2 concentration temperature coefficient must be on the order of 170 ppm per deg C. At that rate, a 2.3 degree C average temperature drop would remove all the CO2 from the atmosphere. It seems quite unlikely that the CO2 concentration temperature sensitivity could be anywhere near this high.
The only other possible natural (or semi-natural if caused by the massive addition of dish-washing detergent to the ocean or deforestation policies on land) would be a large increase in the proportion of CO2 producing bio-forms (animals) as opposed to CO2 consuming bio-forms, (plants) perhaps as a global oceanic bloom of micro-organisms that exhale CO2.
As I understand the author’s article, he is saying that there is a distinction between inorganic and organic CO2 sources and the modern CO2 increases appear to have the signature of organic CO2. In my opinion that does not appear to rule the possibility of modern organic CO2 production-consumption imbalance making a major contribution to our observed CO2 increase. To exclude this possibility, one would have to show that the relative natural organic CO2 production and consumption rates have not changed in recent times.
Dave Springer says:
September 16, 2010 at 4:55 pm
How can you argue that nature sucks up 98.5% of total emissions but only 50% of anthropogenic emissions? An increase in the natural source-rate/sink-rate ratio can just as easily explain the the rate of accumulation. The rate of accumulation has been relatively constant for around thirty years while the rate of anthropogenic emissions has been increasing. It would take only 1.5% change in the natural ratio to decrease the accumulation rate to zero or double it. A natural “dynamic equilbrium” is one of the bad assumptions made by climate modelers that leads to the 98.5% figure that we know varies seasonally by well more than 1.5%.
RW says:
“Smokey: calculations by many groups of scientists have shown that natural variations cannot be the cause of the current warming. Roy Spencer must, I think, have his own idiosyncratic definition of “falsified”.”
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.
And of course, Dr Roy Spencer wins the credibility contest against “RW”. No one has falsified the hypothesis that the observed temperature changes are the result of the same natural variability that has occurred repeatedly in the pre-SUV era..
Sorry, Pamela, but I think you seriously mis-understand some of the science here.
Pamela Gray says:
September 16, 2010 at 5:37 pm
If what we breath out has 4 times more CO2 than what we breath in, with an average -0.5 ratio in human breath, with population growth of 6 billion since the start of the industrial age, and growing exponentially, wouldn’t that affect the ratio as well?
and
The ratio of 12 to 13 is -.5%.
reference http://iopscience.iop.org/1063-7818/32/11/A08
The paper speaks of “respiratory tests and preparations enriched with the stable 13C isotope” so this is a situation where they are intentionally changing the C13 ratios to study what happens. And the “-0.5%” is actually “~0.5%: and that is the “accuracy of carbon isotope ratio measurements in CO2 of exhaled air performed with the TDL”. So after they intentionally enhance the C13 ratio, they can measure the ratio in the exhaled air to within 0.5%.
Pamela:
Please let me try to explain from a completely different direction. Inspired air contains about 0.3 mmHg partial pressure CO2. Exhaled air is about 32 mmHg, so you breathe out air that has about 100 times as much CO2 as you inhale.
But this is not as relevant as the fact that you produce and exhale about .97 kg/day CO2, and it all comes from burning food, either plant or animal matter. That’s 354 kg/year CO2 per person. Fecal production is much smaller at about 0.18 kg/day. Therefore, the atmospheric CO2 you generate from burning food is almost completely returned to the atmosphere rather than stored in your body or dumped into the sewage system. So it doesn’t matter if humans can or do separate 12C from 13C, there would be little net effect on the atmosphere.
How is the uneven distribution of atmospheric CO2 factored into various IPCC models?
R. Gates says:
September 16, 2010 at 12:08 pm
If you believe what GCM’s say about the 40% increase in CO2 since the 1700′s, then the “so what” becomes the significant changes that are climate is undergoing and will be undergoing. If you don’t believe what the GCM’s are saying, then who cares if the CO2 levels are higher than they’ve been for hundreds of thousands of years.
Only an extreme minority currently would ever seriously no doubt that human activity has caused the 40% increase in CO2 since the 1700′s. So while this is an interesting, and mostly accurate post, it is hardly earth-shattering or particularily interesting. The core issue really is how sensitive is the climate system to this anthropogenic based increase in CO2. And of course the next step that some are working on already is some sort of geoengineering efforts to reduce the CO2 levels or mitigate their effects.
Well, golly gee by willikers, Mr. Gates!
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Will you now commence to run around with your underwear over your head, screaming and screeching at the top of your lungs about how all that thar CO2 is a-going to kill us dead?
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The way I see things is thusly: MORE CO2 is beneficial to man than LESS CO2, by dint of the fact that PLANTS NEED that gas to survive.
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More plants = MORE food = HAPPY MAMMALS, avians and other creatures.
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GOT A PROBLEM WITH THAT SITUATION, Mr. Gates?
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Or are you one of them thar people-haters who want to conduct a Pol Pot-style GENOCIDE?
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You’ll be telling us all about that, won’t you?
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Real soon now?
Anthony, I am getting tired. I have been reading these CO2 exegeses too many times. Not your fault. Post certainly gets lots of hits (apparently) and comments. And not my business, but I would greatly appreciate if some of the regulars who seem to have important and valid arguments could act as “peer reviewers” to a poster like Englebeen so that he could present his material and add his answers to the questions or points of other scientists. I feel like the wheels are spinning; too many of the same excellent comments over and over again, but little scientific rigor in getting them together. At the same time I greatly appreciate (almost) all comments and thank those who have the time and energy to continue to post. At this point I think I have “had it” with CO2. Let it continue to grow in the environment and maybe we might remain a little warmer and somewhat more prosperous (or less poor, lots of plants, not as much dependence on rainfall, more efficient energy resources, and maybe we can hold the next glaciation at bay for a longer time).
Still don’t get it. Atmospheric % of CO2 is not anywhere near the % of CO2 in our exhaled breath. Let’s just stick to measuring two vials of air: ambient, and our exhaled breath. If it is a closed balanced system, the two should have equal concentrations. Yes?
There is evidence of a balanced system with vegetation. There is a seasonal variation in atmospheric % of CO2 that balances itself out by growth and decay of vegetation. This can be measured. We can even account for the greening of the planet. More CO2 is taken up, and the same amount is emitted upon decay. Why does this not apply to the animal kingdom? In the case of humans, we just keep populating the Earth more and more. It is not balanced. It would be like having an endless season of vegetative growth (or the reverse: decay) that never quits.
The population curve is interesting. If one were to assume that every person in the hockey stick “working” end is also now driving a car and heating their home with whatever fuel they prefer, it would make sense that a higher standard of living is at fault. But the population growth is NOT in countries with higher standards of living. What else is there about this mass of poorer throngs of humanity that could be emitting more CO2?
From wikipedia so take with a grain of salt.
http://en.wikipedia.org/wiki/Breathing
“The air we inhale is roughly 78% by volume nitrogen, 21% oxygen, 0.96% argon and 0.04% carbon dioxide, helium, water, and other gases. In addition to air, underwater divers often breathe oxygen-rich or helium-rich gas mixes. Oxygen and analgesic gases are sometimes given to patients under medical care. The atmosphere in space suits is pure oxygen. Also our reliance on this relatively small amount of oxygen can cause over activity or euphoria in pure or oxygen rich environments.
The permanent gases in gas we exhale are roughly 4% to 5% more carbon dioxide and 4% to 5% less oxygen than was inhaled. Additionally vapors and trace gases are present: 5% water vapor, several parts per million (ppm) of hydrogen and carbon monoxide, 1 part per million (ppm) of ammonia and less than 1 ppm of acetone, methanol, ethanol (unless ethanol has been ingested, in which case much higher concentrations would occur in the breath, cf. Breathalyzer) and other volatile organic compounds. The exact amount of exhaled oxygen and carbon dioxide varies according to the fitness, energy expenditure and diet of that particular person.”
This change in (there is an increase as well as a change in isotope ratio compared to the air we take in) CO2 is an immediate source of additional CO2, and especially when plants are dormant. You are trying to tell me that this additional and immediate source of CO2 cannot contribute ANYTHING to the measured increasing CO2 at our monitoring stations? Plants take it up immediately? Even in the winter? I still don’t get it. And to reiterate, I’m not talking about any other measurement than the daily, weekly, monthly, and yearly amount of CO2 being measured in the atmosphere. I’m not talking about a model that says this is a closed, balanced system between eating veggies and exhaling.
By the way, I’m not on a kick against having babies. Have however many you want. I’m just trying to explore all the possible sources of this increasing CO2, and that population curve is a very nice fit with the CO2 curve.