Engelbeen on why he thinks the CO2 increase is man made (part 3)

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…

  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).

  1. 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.

  1. 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

  1. 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.

0 0 votes
Article Rating

Discover more from Watts Up With That?

Subscribe to get the latest posts sent to your email.

230 Comments
Inline Feedbacks
View all comments
latitude
September 16, 2010 9:27 am

D. Patterson says:
September 16, 2010 at 7:15 am
Among the many flaws in the essay, the assumption that anthropogenic sources are the only possible explanation for increased d13Carb increases is among the fatal flaws to the argument. It is well known among geologists that the bloom of calcerous marine marine plankton have been responsible for substantially positive excursions of d13C whenever nutrient levels and a warming environment have encouraged their growth and emissions.
==================================================
Same thing on land D.
Fertilizer and soil bacteria
Not even mentioning farming practices, fertilizer and bacteria, made me turn off to this “study”. Makes my opinion of it “total hogwash”

Dave Springer
September 16, 2010 9:28 am

Mike Edwards says:
September 16, 2010 at 9:08 am

There is no doubt that human burning of fossil fuels has dumped a vast quantity of CO2 into the atmosphere and into the oceans. And the changes in isotope ratios found in the atmosphere and the oceans bear testimony to that.

No, it does not bear testimony to that as methane degradation causes exactly the same changes in isotope ratios and appears to be sufficient unto itself to explain it.
Dig it: the industrial revolution began coincident with the end of the Little Ice Age circa 1800. The earth began warming at that time quite naturally unless one can somehow blame the LIA on human activity. A warming earth would naturally release methane from thawing permafrost and with a significant lag time also from the ocean floor. Combine that natural increase in methane emission with the explosive growth in the cattle industry (both beef and milk production) and you have a timeframe that matches the growth in manmade CO2 emission and where the isotope signature is the same for both CO2 contributors.

RW
September 16, 2010 9:39 am

Smokey, of course it follows. You think concentrations would have shot up anyway, if humans had never burned any fossil fuels? How would they have done that?
There has never been a “theory of natural climate variability”. Physics tells us that greenhouse gases play a key role in determining atmospheric temperatures. CO2 is and has always been a greenhouse gas, and if its concentration varies, atmospheric temperatures vary. Fourier and Tyndall discovered this back in the 1800s. How come you’re still ignorant of it?
CO2 is indeed a trace gas. It currently accounts for 0.039% of the atmosphere. Let’s assume you weigh 80kg. Eat 50 μg of Polonium-210 and it will kill you. That’s 0.0000000625% of your mass. So, what’s the relevance of anything being “trace”?

Dan in California
September 16, 2010 10:08 am

Interesting piece of science. I’ve been following this and related topics for about 2 years and have not seen the corresponding calculation check. That is to estimate the tons per year of CO2 being produced in various human endeavors, and compare to the total mass of atmosphere. It should be possible to get within a factor of two. In the US, the Energy Information Administration (EIA) keeps track of fuel use, and we know that a typical 1000 MWe power plant emits about 20,000 tons/day CO2. I can do this estimate unless somebody here points out why it would be useless.
Also – “Marko says: September 16, 2010 at 8:00 am
Roger. If methane is a “fossil fuel” and Saturn’s moon Titan is a big ball of methane it must mean one of two things. Since the scientific concensus claims hydrocarbons are based on organic matter, and who can argue against scientific concensus, Titan was obviously a life bearing moon.”
I have heard astronomer Sir Fred Hoyle argue this is exactly how methane formed on the other planets and moons.

September 16, 2010 10:10 am

Nylo says: “…Anton Uriarte Cantolla…is now a blogger too, and has been a blogger since 2006, and he blogs here. Unfortunately for most of you, his blog is in spanish.”
No problemo. Go to http://babelfish.yahoo.com/ then insert http://antonuriarte.blogspot.com/ in the “translate a webpage” window, select Spanish-to-English, and hit Translate. Vwallah! You can follow most of the text quite easily.

D. Patterson
September 16, 2010 10:24 am

Vince Causey says:
September 16, 2010 at 7:48 am
D. Patterson,
[….]
I think the article is saying that d13 is decreasing not increasing.

Yes, and the rate of sea level rise potentially affecting the d13C levels has been declining. To put it briefly, there are a plethora of confounding factors whose existence has been denied in favor of assuming anthropogenic sources of combustion emissions. Contrary to the article, excursions of isotopic balances have long predated the Industrial Age, and science has barely even begun to acquire the data necessary to untangle the results, much less the causes and effects.

O-C Strat, Oxygen-Carbon Isotope Stratigraphy
The carbon isotope composition of marine limestone fluctuates on a shorter time scale than 87Sr/86Sr ratios (see SrStrat) and the pattern of fluctuation tends to be confined to individual basins. Such relatively short term excursions in marine carbonate d13C values may reflect changes in organic productivity and burial rates of organic carbon. e.g. in the Jurassic and Cretaceous positive d13C “anomalies” may correspond with higher levels of carbon storage in organic-rich mudstone and rising sea levels, while negative d13C excursions may correspond with lower sea levels and/or sub-aerial exposure of shelf areas. This secular variation has been used to correlate limestone strata on a local scale where the original marine carbonate d13C signature has been preserved (e.g. Vahrenkamp 1996).
http://www.isotopic.co.uk/carbonstrat.html

One of the potential anthropogenic effects is the exposure of more mudflats and soils by the human efforts to eradicate mosquitos and malaria by draining vast areas of swamp.

BillD
September 16, 2010 10:27 am

There is valid disagreement on how much the rapid increase in atmophereic C02 is affecting the earth’s climate. However, anyone who has looked at the issue carefully and still does not understand that most of the rapid increase in CO2 is due to human burning of fossil fuels has serious problems unstanding rather simple science.[how so? b.mod]
Reply: This was an inappropriate comment for a moderator to make ~ ctm

RW
September 16, 2010 10:29 am

George E. Smith:
“The NASA map certainly puts the Kibosh on the notion that CO2 in the atmospehre is well mixed; and that appears to be a starting assumption in climate models.”
It’s not a starting assumption in climate models.
“It clearly isn’t even approximately well mixed. To me; well mixed would eman that no matter where or when I took a sample of the atmosphere and analysed it, I would get the same composition on a molecular species (and isotopic) basis; at least within limits of differences that are of no consequence to any climate argument;”
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.

D. Patterson
September 16, 2010 10:32 am

[blockquote]George E. Smith says:
September 16, 2010 at 9:22 am
[….] Why isn’t the ocean exchanging exactly the same isotopic CO2 with the atmospehre whether releasing or taking up ? [/blockquote]
Variations in biological activity at various depths and in different basins of the hydrosphere for one example.

Nullius in Verba
September 16, 2010 10:33 am

I have a bath with a running tap and an open plug hole. There’s one guy controlling the tap, according to unknown rules that depend amongst other things on the water level, and another guy adjusting the flow out through the plug hole, similarly.
We pour a few cubic centimetres of ink into the bath, and the water turns blue.
The water level also rises. Has the colour change proved that the rise in level is caused by the addition of the ink, and not the two guys controlling tap and plug? If the water level had fallen but the water still turned blue, what would you have deduced?
Personally, I am of the opinion that the source of the CO2 is indeed mankind – but I don’t believe this argument proves it. All it shows is that an increasing proportion of the CO2 in the air is fossil-sourced (scarcely surprising), but doesn’t say anything about the cause of the change in overall level. Still, it’s excellent to see the argument/evidence set out and debated. If only the IPCC did the same.

September 16, 2010 10:36 am

The post doesn’t mention precipitation. Doesn’t rain remove CO² from the atmosphere? Is one form of CO² scrubbed preferentially over another? It wouldn’t take much of a difference to throw all the calculations off, would it?

D. Patterson
September 16, 2010 10:44 am

Doug Proctor says:
September 16, 2010 at 9:04 am
HelmutU says:
September 16, 2010 at 6:58 am :
[….]
The recyling of fossil fuel CO2 is certainly a concern.

Is the “recyling of fossil fuel CO2…certainly a concern,” or is the deprivation of CO2 merely a means for meddling humans to unwittingly commit mass suicide as a consequence of CO2 concentrations falling too low to support photosynthesis by the Plant Kingdom?

September 16, 2010 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

Lady Life Grows
September 16, 2010 11:12 am

I was outraged to read Ben’s comment that man is “at fault.”
Englebeen has done a nice job of showing that isotope evidence matches the known fact that humans accelerated burning of “fossil fuels” since around 1850 or thereabouts. He has also quite clearly shown that about half that CO2 has caused a fluorishing of plants.
Where do you get “fault?” I say we are heroes!!
There is no need for another score of posters to whine that maybe the CO2 increase is not anthropogenic.
Your tailpipe feeds the hungry.

Dave Springer
September 16, 2010 11:18 am

BillD says:
September 16, 2010 at 10:27 am
There is valid disagreement on how much the rapid increase in atmophereic C02 is affecting the earth’s climate. However, anyone who has looked at the issue carefully and still does not understand that most of the rapid increase in CO2 is due to human burning of fossil fuels has serious problems unstanding rather simple science.[how so? b.mod]

No Bill. The argument made is a logical fallacy called an argument from ignorance. The carbon isotope ratios are analyzed, the sources of different istopes are analyzed, known natural sources are ruled out, and then the question is asked: If not fossil fuel then what else could it be?
The what else is methane which in less than 10 years degrades into water vapor and CO2 and most importantly for this discussion it causes the same isotope signature that burning of fossil causes. Some or even most of the 150% rise in atmospheric methane since the industrial revolution could be man-made. It’s estimated that the cattle industry contributes 16% of total annual emission. Anaerobic decomposition in landfills and other waste disposal generates methane. Methane is present in large quantities along with fossil fuel deposits. Methane vented from active coal mines contributes an estimated 10%. It is also released from oil wells and natural gas wells. As well it is released by thawing permafrost and warming ocean bottoms.
I was quite surprised to find that although the OP included a drawing showing methane as being twice as effective in abililty to alter carbon isotope ratios yet it was not even mentioned in the analysis – like the proverbial elephant in the room.
While there is no doubt in my mind that fossil fuel burning contributes to some fraction of the observed isotope ratios it’s pretty clear that methane does the same thing and in fact could be the dominant factor in changing carbon isotope ratio. Yet methane wasn’t even mentioned in the analysis!
Perhaps you or someone else can explain why the analysis failed to see the elephant sitting in the corner of the room.

Bob Shapiro
September 16, 2010 11:24 am

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.
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?!

Pamela Gray
September 16, 2010 11:29 am

I could be all wet here. So take this with a grain of salt. I had a hard time finding the answer. I found one source that talk about it. Humans respire 13CO2. Has anyone calculated the increase in this isotope as a function of the increasing animal population? With the greening of the planet, other animals that respire this isotope would also be more abundant given a more abundant food supply.
Could this be at least a part of the extra 13CO2 in the atmosphere?

Dan in California
September 16, 2010 11:54 am

” Pamela Gray says: September 16, 2010 at 11:29 am
I could be all wet here. So take this with a grain of salt. I had a hard time finding the answer. I found one source that talk about it. Humans respire 13CO2. Has anyone calculated the increase in this isotope as a function of the increasing animal population?”
Pamela: The carbon isotope ratio that you respire is identical to the isotope ratio of the carbon in the food you eat. The human body is a chemical reactor, not a nuclear reactor. Both 13C and 12C are stable, but 14C is radioactive and Beta decays with a 5730 year half life, too slow to change the isotopic ratio inside your body. When you die, the 14C decays and the ratio can tell us when you died, up to about 60,000 years, or 10 half-lives.

Pamela Gray
September 16, 2010 11:54 am

The ratio of 12 to 13 is -.5%.
reference http://iopscience.iop.org/1063-7818/32/11/A08
World population between 1850 and 2011 has increased by 6 to 7 billion people.
reference http://geography.about.com/od/obtainpopulationdata/a/worldpopulation.htm
We breath out between 252 Kg/yr and 525Kg/yr. We make our own so there is not a balance between what we take in as food and what we breath out. This number has not considered the increase in all animal populations as a result of the greening of the planet.
reference http://wiki.answers.com/Q/How_much_CO2_is_exhaled_by_the_average_human_each_year

Pamela Gray
September 16, 2010 11:59 am

So if we are breathing out more 13CO2 along with more 12CO2 due to population growth, and the greening of the planet prefers 12CO2, human population growth could be causing at least some of the extra 13CO2 in the atmosphere.
Wonder what restrictions and taxes will be placed on that issue.

Chris Knight
September 16, 2010 11:59 am

I would like to ask one question – if all geologic carbon – coal, oil, carbonate etc., were in the atmosphere, what would the percentage of CO2 be?
Sorry, I meant I would like to ask two questions – how much hotter would it be then?

R. Gates
September 16, 2010 12:08 pm

899 says:
September 16, 2010 at 6:00 am
This is all very interesting, but so what?
The level of CO2 in the atmosphere has been far higher than present, and things were copacetic then.
____________
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.

Nullius in Verba
September 16, 2010 12:16 pm

Chris Knight,
Look up the theories on the Earth’s atmosphere during the Hadean era. They’re based on the idea that most of the Earth’s carbonate resources were in the atmosphere.

Dave Springer
September 16, 2010 12:17 pm

http://ethomas.web.wesleyan.edu/ees123/clathrate.htm

Unique features of clathrates as part of the carbon cycle
Methane hydrates are part of the carbon cycle with unique features: they serve as a possible large source of isotopically extremely light carbon, but NOT as a sink. The carbon in methane hydrate was originally stored in the sediments (lithosphere, out of contact with the ocean and atmosphere) as organic carbon. Thus only carbon with the isotopic signature of organic carbon is taken out of the ocean-atmosphere reservoir – influencing the carbon isotopic value of the remainder in the well-known way (ratio of organic carbon to carbonate of sediments). Within the lithosphere, isotopically light carbon is strongly enriched in the methane in gas hydrates by bacterial action. The isotopically heavier remainder is isotopically not much heavier than ‘normal’ carbonate, and ends up in carbonate in the lithosphere. As long as both the methane hydrates and the remainder remain in the sediments there is no effect on the exospheric carbon reservoirs, but when the methane hydrates dissociate, material strongly depleted in the heavy isotopes escapes from the lithosphere into the ocean-atmospheric reservoir – making that reservoir lighter. The effect on the large sediment reservoir is not noticeable.
This means that the carbon that is stored in the methane hydrates was taken from the ocean-atmosphere system as carbon with an average isotopic composition of about -25‰, but the carbon returning to the ocean atmosphere system through the methane hydrate loop is isotopically ~ -60‰. Overall decreasing methane hydrate reservoirs (e.g., as a result of fluctuating sea levels during glacial -interglacial alternation) thus lead to a secular trend towards a lighter carbon isotopic signature of the ocean-atmosphere reservoir.

Pamela Gray
September 16, 2010 12:20 pm

Dan, your reply is too simplistic. Our isotopic ratio of what we breath out may or may not be based on what we breath in or eat. There are many variables to take into account related to exhaled composition and ratios of CO2.