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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RW,
“And that is precisely what we see in the map. The colour scale ranges from about 365 to 385ppm – a global variation of no more than 3% either side of the mean. This is of no consequence to any climate argument.”
No consequence? Let’s look at the increase in radiative forcing that would occur by going from 365 to 385 ppm. Using the IPCC as source, dF = 5.85Ln (C1/C0).
Calculating the respective dF for 385 and 365 ppm and deriving the ratio, we get
Ln(385/280) / Ln(365/280)
= (Ln385- Ln365) / (Ln365 – Ln280)
=0.318/0.264
=1.2
In other words, that teensy weensy 3% translates to a forcing increase of 20% more as we go from 365 to 385ppm. It sometimes pays to do some basic checking before shooting from the hip.
Yeah, “Only an extreme minority currently would ever seriously no doubt that” the Emperor is wearing no clothes.
Responding to BillD, Dave Springer says:
“The argument made is a logical fallacy called an argument from ignorance.”
If it were not for the alarmists’ argument ad ignorantium, the scare ’em crowd wouldn’t have much left to say. The argument from ignorance concludes with the belief that a harmless and beneficial trace gas is the main driver of climate change “because we can’t think of any other reason.” The alarmist crowd is terrified to death of the Scientific Method, preferring ad-hom arguments and illogical, one-sided propaganda like Al Gore’s AIT.
RW tries to re-frame the argument, avoiding the question by substituting a false strawman: “There has never been a ‘theory of natural climate variability’.”
Ignorance is no excuse. Dr Roy Spencer has been quoted here before: “No one has falsified the hypothesis that the observed temperatures changes are a consequence of natural variability.”
So who should we listen to? An internationally esteemed climatologist, and to planet Earth – which has not boiled over as demanded by grant-sniffing climate modelers?
Or to… “RW”?
In the 400 years before, there is only a small variation, probably caused by the temperature drop in the Little Ice Age.
There was no such change in CO2 during the Spoerer minimum, so either it was not colder then or the drop has little to do with temperature.
The IPCC and other Alarmists claim anthropogenic fossil fuel combustion is responsible for about 4 to 5 gigatons of carbon dioxide per year of which only 1.5 gigatons remains unsequestered by the environment that sequesters the other 110 gigatons of natural carbon dioxide emissions. So, if you believe that a 3% variance in the global carbon dioxide concentrations is too insignificant to take notice, why should you believe an approximate 1.5% to 3% increase of anthropogenic carbon dioxide, according to the IPCC bookkeeping, is supposeed to be Alarming?
I have never doubted that the increase in CO_2 levels was real, and that the burning of fossil fuels has contributed significantly to it. It is also clear to me that the Earth has warmed over the last quarter of the 20th century, although the extent of the warming is uncertain since the data has been manipulated in an untrustworthy way. I am doubtful that increased CO_2 is entirely responsible for the observed warming – in fact most of it seems to me to be cyclical and natural. The models are not worth spit and I believe the sensitivity of the climate to increased CO_2 has been considerably overtstated. I am extremely skeptical that the observed warming and higher CO_2 levels are likely to be harmful.
The point is that people are skeptical about different aspects of the AGW story. Since this is one aspect of the story about which I am not skeptical, it is interesting to watch the responses of those who are.
From the paper referenced by Engelbeen above: “But in contrast with what happens during photosynthesis, in the process of calcite precipitation into shells of marine organisms there is no isotopic discrimination with respect to the ratio 13C/12C of marine waters.”
Yes, photosynthesis does discriminate 13C and 12C, which is the basis for this thread. But just as marine animal shell production does no isotopic discrimination, I found no reference to animal (or human-only) isotopic discrimination in oxidative metabolic processes. I would be interested in seeing such a discussion.
Trend without end, Amen.
All trends lead to Warming.
A trend for all seasons.
In Trends we Trust.
This Trend ain’t big enough for both of us.
——————-
Don’t trend on me.
Take this trend and shove it, I ain’t going there no more.
Trender Bender: When hysteria meet the brick wall of reality.
Take the last Trend to Warmsville, and I’ll meet you at the Glacier.
Four score and 7 Trends ago.
This reaction is exothermic:
CO2+GWR=BS
Jaraj V said, “It is beating a dead horse. Until someone recognizes the warming effect of additional CO2 in polar regions, which have low humidity and therefore the “greenhouse effect” should be strengthened most, the discussion is equal to “how many angels have to push planets to fly on their orbits.” ”
Let’s not forget that this warming in the Arctic would be rather weak. Who cares if it’s -31.0 rather than -31.1 deg C? It’s not going to change the climate that anyone would notice.
The Arctic ice melting depends largely on warm air from the South and not solar energy during the summer. The low angle, reflection, and travel distance through the atmosphere attenuate solar input to less than 3% of direct overhead sunlight. This energy, hitting water, would heat it ever so little and this energy would be lost to evaporative cooling almost immediately. Hitting ice, lot’s of reflection, little effect. Then, there is the occasional influx of warm water into the Arctic basin, very effectively melting the ice from below.
I wonder, so what if we increase CO2? It does not warm the climate in any way that makes detectable changes and it helps the plants, the marine life, the corals (acidification, if any at all, is trumped by adaptation and tolerance), and our food supply. There’s no down side here.
Congrats Ferdinand.
I’ve enjoyed every one of your patient logical explanations.
I’m still waiting for someone to offer any evidence that burning fossil fuels will cause
a net decrease in C02.
#
#
wsbriggs says:
September 16, 2010 at 5:28 am
My understanding, small though it may be, is that this paper is substantially challenged by Chiefio’s musings on the subject (sorry, I can’t find my pointer to the article). There, the discussion of the carbon isotope ratio covers also the behavior of plankton in the oceans, net, net, the ratio is not maintained.
_________________________________________________________
I have that pointer bookmarked
The Trouble With C12 C13 Ratios:
http://chiefio.wordpress.com/2009/02/25/the-trouble-with-c12-c13-ratios/
F.E.
Thank you for your comment inducing Part 3. You obviously spent a significant amount of time on it. You do know how to stimulate discussion.
I have no position on whether man has caused the industrial age increase in atmospheric CO2. This is because I am waiting for sufficient or even partial significant evidence of it.
I do not see any significant evidence in your Part 3 with respect to whether man has caused the industrial age increase in atmospheric CO2.
You said in the final paragraph of Part 3,
Another thing it does not prove (directly or indirectly) is that industrial era atmospheric CO2 conc net increases must be caused (in whole or in part) by our fossil fuel CO2 emissions; in spite of no one denying that man put increased amounts of CO2 yearly into the atmosphere from fossil fuel emissions during the whole industrial age. In other words, as Paul Birch more simply said in a comment to your Part 1 on August 5, 2010 at 12:06 pm ;
I sincerely hope there will be a Part 4 where you provide evidence showing proof that the industrial era CO2 atmospheric conc increase has been caused by man’s undeniable increases in yearly CO2 emissions from burning fossil fuels.
I also note that your part Part 1 & Part 2 contained similar issues as this Part 3. For reference those posts were:
F.E., in closure, thank you again, these past posts are interesting but I think most of us would rather like to see evidence showing proof of how CO2 increases in the atmosphere cause warming or other effects. We are looking forward to that.
John
Smokey:
“natural variablity” is not a theory. It is the absence of a theory. It is a statement that says “things change” which is pretty much a meaningless statement unless you put numbers on it. Things fall to earth is not a theory, although it is true. you seem to think that “natural variability” is somehow the logical opposite of AGW. Its not.
1. GHGs warm the planet AND the data show unexplained variability
when you can demonstrate that the above is false or that either side implies the negation of the other side, then you have something. Simply, it does not follow from the fact that GHGs warm the planet, that there will be no unexplained variability in the data. And neither does it follow from the observation of unexplained variability in the data that GHGs do not warm the planet. neither of these follow because both sides of the conjunction happen to be true.
“”” Fred H. Haynie says:
September 16, 2010 at 10:51 am
George E. Smith said on Engelbeen on why he thinks the CO2 increase is man made (part 3)
September 16, 2010 at 9:22 am
There will be some fractionation each time CO2 is emitted from or absorbed by water because of the 45/44 molecular weights ratio. This fractionation process can explain the seasonal cycle just as well or better than seasonal growth cycle of plants. http://www.kidswincom.net/climate.pdf “””
Well I suppose it is reasonable for those processes to vary with molecular weight.
So just what are the water/atmosphere ratios (equilibrium) for the following species:-
16O12C16O, 16O13C16O, 16O12C18O,16O13C18O, 18O12C18O, 18O13C18O Just the values at some nominal normal Temperature would be useful; but graphs versus Temperature would be more helpful.
Also what are the take up ratios for each of those species in the growing plants .
I’m sure they are all different; but are they all properly accounted for in the models. And given that the CO2 abundance can vary by 3% over the globe; how to they collect that data for each of the weather measuring stations so they can correlate their Temperature anomalies with their local CO2 abundance to get a global summary.
That was the point of my observation that atmospheric CO2 is not well mixed. Too bad there isn’t a similar color map showing the global amount of seasonal variation in the atmospheric CO2. It may be 6 ppm p-p for ML, but it is 18 ppm p-p for pretty much all of the arctic oceanic region. and at the south pole it is more like -1 ppm p-p; being out of phase with the northern cyclic variations.
That data suggests a lot of rapid transfer between the oceans and the atmosphere, since in the Arctic, that 18 ppm drop happens in just 5 months; so that is hardly time for any deep ocean biologic processes to affect what is most likely a simple segregation coefficient at the water/air interface..
And if the13C/12C take up at the ocean surface is a drmatic as RW suggests, isn’t that interchange causing its own shift in the atmospheric CO2 isotopic ratios.
[Just for Pamela: Did you have a great day?]
The CO2 atmospheric concentration plot seems to correlate most with an active ocean rather than industrial areas. For example, most of Europe shows low CO2 and so does eastern North America. The west coast of North America has very active sea life due to upwelling of deep ocean water there (cold). The Gulf Stream appears to have very high CO2 levels, as does the Mediterranean (both warm). The Western Pacific also has higher CO2 levels according to the map, and so does the eastern Indian ocean.
It isn’t at all clear that humans are responsible. The map does point to the oceans as being the prime source of CO2.
Interestingly, there are many areas with low CO2 concentrations. The tropical regions of South America, Africa, and Borneo. Equatorial waters seem to be sinks.
If you wanted to blame industrialization for CO2, why does Japan have such a low concentration? Why does the industrial area around Hong Kong have a lower CO2 concentration than California? Why does India seem to be more of a sink than a source despite having a population of about 1 billion people?
It appears far more likely that methane is the source of CO2, via methanotrophic bacteria. They are found in all waters, and are associated with methane vents such as the California coast from Santa Monica to Oregon, the mid-Atlantic ridge, and the Black Sea. See http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446507/.
Mud volcanoes in the Mediterranean Sea produce very methane-rich sediments that are strongly depleted in 13C. See http://aem.asm.org/cgi/content/full/66/3/1126.
The Caspian Sea and the Sea of Okhotsk are also major sources of methane. These are both high CO2 features on the CO2 map. See http://books.google.com/books?id=r_2Ia8wOBlgC&pg=PA138&lpg=PA138&dq=methane+caspian+sea&source=bl&ots=0p6fuf40C8&sig=GnKSIBCGk8hIiqDPRgcqjE3ZJMQ&hl=en&ei=T4WSTIOLG42CsQPts5zACg&sa=X&oi=book_result&ct=result&resnum=6&ved=0CCYQ6AEwBQ#v=onepage&q=methane%20caspian%20sea&f=false.
If we could see the same map of methane distribution in the atmosphere, we would have our answer. It turns out we can. See http://photojournal.jpl.nasa.gov/browse/PIA09941.jpg.
But what does that image show? At first it appears that the test failed. But if you notice, the methane has highest concentrations surrounding the areas we noticed had high CO2 concentrations. Could it be that we are simply seeing depletion of methane by conversion to CO2? And there are other sources of methane, like Antarctica, where the CO2 conversion apparently doesn’t take place. How many methanotrophs would we expect to find in Antarctica?
It seems we keep over-estimating the impact of people. 7 billion people can’t do all that much compared to bacteria.
PeterB in Indianapolis says:
September 16, 2010 at 8:02 am
….Your conclusion assumes that there are no other chemical reactions going on than the one you listed, and that O2 is the “limiting reagent” for the equation you listed. Let me assure you that there are BIG reactions going on all of the time which counterbalance the reaction that you showed, and as such, it is HIGHLY unlikely that O2 is the limiting reagent.
Something truly bizzare would have to happen for the world to run out of Oxygen any time in the next few billion years.
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Some bizzare thing like idiotic humans managing to sequester CO2 and dropping the atmospheric level below 180PPM – ALL plants would then die.
What I found truly amazing was this plant/CO2 study:
Plant photosynthetic activity can reduce the Co2 within the plant canopy to between 200 and 250 ppm… I observed a 50 ppm drop in within a tomato plant canopy just a few minutes after direct sunlight at dawn entered a green house (Harper et al 1979) … photosynthesis can be halted when CO2 concentration approaches 200 ppm… (Morgan 2003) Carbon dioxide is heavier than air and does not easily mix into the greenhouse atmosphere by diffusion… Source
Think about it a plant can drop the CO2 in its vicinity by 50ppm in minutes!
Another key piece of evidence that we’re living on a planet with CO2 levels currently at the very bottom of the normal range is the whole new group of plants that evolved several million years ago to cope withthe low levels of CO2. They developed a new method of photosynthesis called C4 which permits greater water efficiency and the ability to photosynthesise in higher temperatures at greatly reduced CO2 levels.
An even better adaption called CAM evolved in plants like cacti.
At 200 pm CO2 trees starve http://biblioteca.universia.net/ficha.do?id=912067
(Since I last looked this reference has been removed from the internet. It does not correlate well with the Ice core data.)
However stomata data by Wagner, Aaby and Visscher prove that the ice core data is seriously in error. The ice core data can be corrected using J.J.Drake’s correlation, the profile does not change but the ppm values do so the analysis is still valid.
http://www.bio.uu.nl/~palaeo/people/Rike/index.html
Actual Paper.
http://www.pnas.org/content/99/19/12011.full.pdf
The whole “official” CO2 historic measurement is called into question by this paper. It looks at the dogma and politics behind the 70 years of CO2 measurement as well as the science. It is a very interesting read. http://www.co2web.info/ESEF3VO2.pdf
More Info:
Plant Stomata react more accurately to CO2 concentration, as has been determined in experiments. (More CO2 means fewer stomata, as plants exchange CO2 more efficiently) Historical collections of leaves can be used to determine past CO2 levels. In most cases, researchers are bound by the modern paradigm, and get confused by the low stomata counts of the past. Stomata cannot measure very high CO2, but only indicate high C)2. Higher CO2 levels over 325ppm are underestimated. When reading stomata research, you need to filter out the ruling paradigm when the problematical ice-core data is used to calibrate the stomata, when it should be the reverse.
Rapid atmospheric changes are well known from past reconstructions:
See http://www.ncbi.nlm.nih.gov/pmc/articles/PMC129389/pdf/pq1902012011.pdf
& http://www.geocraft.com/WVFossils/Reference_Docs/Late_Holocene_CO2_3000-4300_BP_Jessen_etal_2005.pdf
Changes of close to 100ppm in a century are quite common.
Speaking of Volcanoes:
The true extent to which the ocean bed is dotted with volcanoes has been revealed by researchers who have counted 201,055 underwater cones. This is over 10 times more than have been found before.
The team estimates that in total there could be about 3 million submarine volcanoes, 39,000 of which rise more than 1000 metres over the sea bed. http://www.newscientist.com/article/dn12218
Volcano Outgasing of CO2.
“The primary source of carbon/CO2 is outgassing from the Earth’s interior at midocean ridges, hotspot volcanoes, and subduction-related volcanic arcs. “http://www.columbia.edu/~vjd1/carbon.htm
Steven mosher says:
” ‘natural variablity’ is not a theory.”
I prefer Dr Spencer’s climate null hypothesis:
No one has falsified the hypothesis that the observed temperature changes are a consequence of natural variability.
Steven mosher says:
September 16, 2010 at 2:05 pm
Smokey:
“natural variablity” is not a theory. It is the absence of a theory. It is a statement that says “things change” which is pretty much a meaningless statement unless you put numbers on it. Things fall to earth is not a theory, although it is true. you seem to think that “natural variability” is somehow the logical opposite of AGW. Its not.
You are sailing very close to argumentum ad ignorantium, i.e.
“We won’t accept natural variability as an argument because:
it is not difficult to find some aspect of natural chaotic non-equilibrium emergent pattern variability that is not fully understood and mathematically described to the finest detail.”
Follow this logic and you will find we know nothing at all about anything.
Natural variability is a perfectly valid null hypothesis.
A null hypothesis is a valid way to approach any scientific question.
The CAGW hypothesis cannot survive the scientific process any more than anaerobic bacteria can survive in the presence of oxygen.
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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.
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.
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.
John
Bob Shapiro says: “Let’s assume for a second that there are no equilibrium processes which would have CO2 at current levels, even if humans didn’t exist.”
Let’s not. You’re begging the question.
“Humans do produce some amount of CO2, and added to the net CO2 from all other processes, the total is higher than it would have been, meaning that humans have produced the incremental CO2. So now, granted all this, what is your point?!”
The incremental CO2 may be negligible.
Why would anyone in their right mind WANT to “cause a net decrease in CO2″?
What does Steve McIntyre think about this?
Man contributes 3.27% of the CO2, Nature 96.73%. What’s the problem?