Numeracy in Climate Discussions – how long will it take to get a 6C rise in temperature?

The answer may surprise you

Note: This essay is a result of an email discussion this morning, I asked Dr. Happer to condense and complete that discussion for the benefit of WUWT readers. This is one of the most enlightening calculations I’ve seen in awhile, and it is worth your time to understand it because it speaks clearly to debunk many of the claims of temperature rise in the next 100 years made by activists, such as the 6c by 2050 Joe Romm claims, when parroting Fatih Birol in Reuters:

“When I look at this data, the trend is perfectly in line with a temperature increase of 6 degrees Celsius (by 2050), which would have devastating consequences for the planet,” Fatih Birol, IEA’s chief economist told Reuters.

dec11-eleven-degrees2[1]

Graph source: IEA.org scenarios and projections

– Anthony

Guest post by Dr. William Happer

For any rational discussion of the effects of CO2 on climate, numbers are important. An average temperature increase of 1 C will be a benefit to the planet, as every past warming has been in human history. And the added CO2 will certainly increase agricultural yields substantially and make crops more resistant to drought. But in articles like “Scant Gains Made on CO2 Emissions, Energy Agency Says” by Sarah Kent in the Wall Street Journal on April 18, 2013, we see a graph with a 6 C temperature rise by 2050 – if we don’t reduce “carbon intensity.” Indeed, a 6 C temperature rise may well be cause for concern. But anyone with a little background in mathematics and physics should be able to understand how ridiculous a number like 6 C is.

The temperature change, ∆T , from the mean temperature of the present (the year 2013), if the concentration N of CO2 is not equal to the present value, N = 400 ppm, is given by the simple equation

Happer_equation1(1)

Here ∆T2 is the temperature rise that would be produced by doubling the CO2 concentration from its present value, and ln x denotes the natural logarithm of the number x.

The proportionality of the temperature increment ∆T to ln N is widely accepted. But few know that this is a bit of a “miracle.” The logarithmic law, Eq. (1) comes from the odd fact that the average absorption cross section of infrared light by CO2 molecules decreasesvery nearly exponentially with the detuning of the infrared frequency from the 667 cm1 center frequency of the absorption band. More details can be found in a nice recent paper by Wilson and Gea-Banacloche, Am. J. Phys. 80 306 (2012). Eq. (1) exaggerates the warming from more CO2 because it does not account of the overlapping absorption bands of water vapor and ozone, but we will use it for a “worst case” analysis.

Recalling the identity for natural logarithms, Happer_equation2  , we write Eq. (1) as

Happer_equation3   (2)

The only solution of the equation ln x = ln y is x = y, so (2) implies that

Happer_equation5   (3)

Recent IPCC reports claim that the most probable value of the temperature rise for doubling is ∆T2 = 3 C. Substituting this value and a warming of ∆T = 6 C into Eq. (3) we find

Happer_equation6   (4)

But the rate of increase of CO2 has been pretty close to 2 ppm/year, which implies that by the year 2050 the CO2 concentration will be larger by about (5013) years×2 ppm/ year = 74 ppm to give a total concentration of N = 474 ppm, much less than the 1600 ppm needed.

The most obvious explanation for the striking failure of most climate models to account for the pause in warming over the past decade is that the value of ∆T2 is much smaller than the IPCC value. In fact, the basic physics of the CO2 molecule makes it hard to justify a number much larger than ∆T2 = 1 C – with no feedbacks. The number 3 C comes from various positive feedback mechanisms from water vapor and clouds that were invented to make the effects of more CO2 look more frightening. But observations suggest that the feedbacks are small and may even be negative. With a more plausible value, ∆T2 = 1 C , in Eq. (3) we find that the CO2 concentration needed to raise the temperature by ∆T = 6 C is

Happer_equation7   (5)

This amount of CO2 would be more than a warming hazard. It would be a health hazard. The US upper limit for long term exposure for people in submarines or space craft is about 5000 ppm CO2 (at atmospheric pressure). To order of magnitude, it would take a time

t = 25, 600 ppm/(2 ppm/year) = 12,800 years.

(6)

to get 6 C warming, even if we had enough fossil fuel to release this much CO2.

A 6 C warming from CO2 emissions by 2050 is absurd. It is a religious slogan, a sort of “Deus vult” of the crusade to demonize CO2, but it is not science.

=============================================================

Dr. William Happer is the Cyrus Fogg Brackett  Professor of Physics at Princeton University, and a long-term member of the JASON advisory group,where he pioneered the development of adaptive optics. From 1991-93, Happer served as director of the Department of Energy’s Office of Science.

UPDATE: Dr. Happer has contacted the author of the paper cited, and he has graciously setup a free link to it: http://comp.uark.edu/~jgeabana/gw.html

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ferd berple
April 18, 2013 8:34 pm

Konrad says:
April 18, 2013 at 8:04 pm
Radiative cooling at altitude is critical for continued convective circulation… Energy loss at altitude is just as important for convective circulation as energy input near the surface.
=========
correct. without ghg the atmosphere would be isothermal and there would be no vertical circulation.
Instead the vertical circulation removes heat from the surface, where GHG radiates 1/2 this energy to space and returns 1/2 to the surface. This removes a net 1/2 of the energy that would otherwise not be removed, and balances the radiative transfer for no net warming long term. This yields the minimum energy solution that nature always seeks in dynamic systems.

April 18, 2013 8:38 pm

A characteristically elegant and beautifully simple analysis by Will Happer.

Richard D
April 18, 2013 8:45 pm

kirkmyers says:
April 18, 2013 at 7:03 pm
“There is plenty of research challenging the man-made-CO2-is-warming-the-earth theory. And that’s all it is: a theory.”
______________________________________________________________
I disagree. As demonstrated by empirical data, It’s a failed hypothesis.

RoHa
April 18, 2013 9:15 pm

kirkmyers says:
April 18, 2013 at 7:03 pm
“There is plenty of research challenging the man-made-CO2-is-warming-the-earth theory. And that’s all it is: a theory.”
______________________________________________________________
Richard D says: I disagree. As demonstrated by empirical data, It’s a failed hypothesis.
I say it isn’t even that. I don’t think it was well-formed enough to be a hypothesis. It was an overblown speculation.

GeeJam
April 18, 2013 9:38 pm

Sam the First says:
April 18, 2013 at 7:30 pm
We have a public meeting tomorrow night . . . . can anyone suggest some pertinent questions I can ask [Tim Yeo] without getting too technical so that other attendees can’t follow the import of them?
Response: Suggest you ask “If CO2 is the main cause of climate change, in ppercentage terms, how much CO2 is in the atmosphere when compared to all other gases in the air, and what proportion of this total CO2 amount is man-made?”
To support you (if you haven’t already seen it), the following non-scientific simple analogy may help (first posted Feb 26 on WUWT) . . . .
“If the Earth’s atmosphere were represented by a large swimming pool filled with 3,200 gallons of water:
2,498 gallons would be Nitrogen (78.084% of atmosphere by volume),
670 gallons would be Oxygen (20.9476% of atmosphere by volume),
30 gallons would be Argon (0.934% of atmosphere by volume),
1 gallon would be a mixture of Methane (0.002%), Neon (0.001818%), Helium (0.000524%), Krypton (0.000114%), Hydrogen (0.00005%) and Xenon (0.0000087%)
and
1 gallon would be Carbon Dioxide (0.0314% of atmosphere by volume).
Of the SINGLE GALLON of Carbon Dioxide, SEVEN and THREE QUARTER PINTS are naturally occuring. This leaves a QUARTER OF A PINT (5 fluid ounces) which is man-made. If this amount was a small 5 fl.oz. bottle of Red Food Colouring and we poured it in to the other 3,200 gallons of water in the pool, how much will it affect the colour of the water? We’ll even give you a big whisk so that you can mix it up as much as you like. Go on, have a go.
Unfortunately, some people visualise that all the water in our swimming pool has now turned an intense shade of bright red – so a reason for taxing people (including CO2 emmisions based vehicle excise duty in the UK).
Meanwhile, the rest of us all huddle patiently around the edge of our swimming pool looking puzzled as we stare through the transparent depths of beautifully clear water to the bottom – and wondering why the world’s political figures continue to spend billions trying to prevent the screw cap coming off the top of a small 5 fl.oz bottle of red food colouring.”
Best of luck for the meeting.
For full link, see
http://wattsupwiththat.com/2013/02/26/new-survey-shows-climate-change-still-not-catching-on-as-a-concern/

rgbatduke
April 18, 2013 10:15 pm

When you take a moving atmosphere into consideration, radiative gases cool at all concentrations above 0.0ppm. Adding radiative gases to the atmosphere will only speed up convective circulation and tropospheric cooling. At 0.04% there is no hope of measuring any such effect from CO2. This is why the models keep failing.

An interesting argument. However, I’d like to see more than just a verbal argument. Do you have any computations or numbers to support it? Or even a very simple model?
I agree with a lot of your assertions, e.g. the practical irrelevance of the adiabatic and hence essentially reversible ALR — the only mechanism that actually cools the atmosphere (permanently removes heat from it) is radiation, and that occurs in the upper troposphere where the atmosphere ceases to be opaque to e.g. LWIR (although it is more complex than this, this process occurs in depth and at different depths in different frequencies). But I find it somewhat difficult to believe that all of the climate models in the climate modeling universe ignore heat bulk transport either vertically or laterally. After all, it isn’t just dry air that carries up the heat — a lot of energy gets lofted up in the form of latent heat of vaporization of water, for example.
So, any papers, computations, models, actual evidence to support your assertion? I don’t have a good enough feel for the numbers to be able to assess whether or not to take this seriously, so you’ll have to help me out if you want me to believe it.
rgb

ScepticKnitter
April 18, 2013 10:38 pm

CO2 absorbs a specific bandwidth of light.
Is there an article or paper somewhere that discusses the percentage of that bandwidth that is absorbed by CO2 and what percentage of that bandwidth escapes the Earth’s atmosphere?
If x ppm of CO2 would absorb 100% of the bandwidth of light…then x +1 ppm CO2 or 10x ppm CO2 does not make a bit of difference. Right? This article talks about the potential to reach 1600ppm in the distant future…would it matter? At how many ppm would CO2 absorb 100% of the energy/light available?
….Or, does the current CO2 level of 400 ppm absorb such a small percentage of the available bandwidth of light, that this is a silly question?
This is a great site and I would really appreciate a link to some further reading. Those of us who got a college degree is a less than hard science are trying to keep up! 🙂

rgbatduke
April 18, 2013 10:45 pm

“If the Earth’s atmosphere were represented by a large swimming pool filled with 3,200 gallons of water:
2,498 gallons would be Nitrogen (78.084% of atmosphere by volume),
670 gallons would be Oxygen (20.9476% of atmosphere by volume),
30 gallons would be Argon (0.934% of atmosphere by volume),
1 gallon would be a mixture of Methane (0.002%), Neon (0.001818%), Helium (0.000524%), Krypton (0.000114%), Hydrogen (0.00005%) and Xenon (0.0000087%)
and
1 gallon would be Carbon Dioxide (0.0314% of atmosphere by volume).

I’m puzzled. First, 3200 gallons of water is a tiny, tiny swimming pool — about six feet by nine feet by six feet deep, or a bit wider if you want to make it shallower.
Second, slightly over one gallon is then not CO_2, but CO_2 and ALL THE REST of the trace gases put together. See e.g. http://en.wikipedia.org/wiki/File:Atmosphere_gas_proportions.svg.
Of these trace gases, there is no point in listing any of them but CO_2. But OTOH, this list leaves out the highly variable but roughly 1% of the troposphere that is water! As for what proportion of the gallon-plus that is CO_2 is “man made” or attributable to humans — that is debatable, but the debate is not served by presenting a pretty metaphor as if it is a fact. Pre-industrial CO_2 was around 300 ppm. That’s a fact. It is around 400 ppm now. That, too, is a fact. One argument, then, might make a full quart of your gallon human contributed CO_2. Another one — arguing that the bulk of the additional CO_2 is actually oceanic CO_2 released by warming — might make it less, but then one would have to explain how it appears that the actual measured concentration of CO_2 in the ocean appears to be at the very least holding its own if not increasing, if it is simultaneously the cause of more CO_2 in the air. At the very least, you should justify any number you cite, and be prepared to defend it, because ANY number that gets cited, either way, is highly dependent on the model used to compute it and the interpretation of measurements that are not at all straightforward to interpret.
Finally, at the end, after one gets through the entire tedious metaphor (correcting it along the way) one is forced to say — so what? It is a simple, measurable, observable fact that the one “gallon” of CO_2 in the “pool” is sufficient to be totally opaque to IR in its absorption bands from the surface all the way up to near the top of the troposphere, where the “murkiness” of the pool finally diminishes enough so that IR in this channel can escape to space. And what of the 30 gallons of the water that are — um — water?
Note well that I’m not asserting that CO_2 is or is not damaging or deadly, only that this metaphor might not be what one wants to present at any meeting or public discussion where you want to actually convince somebody that it is harmless, or that there is no such thing as the GHE, or whatever.
rgb

rgbatduke
April 18, 2013 10:49 pm

CO2 absorbs a specific bandwidth of light.
Is there an article or paper somewhere that discusses the percentage of that bandwidth that is absorbed by CO2 and what percentage of that bandwidth escapes the Earth’s atmosphere?

David referenced Ira Glickstein’s article earlier. I keep the link handy:
http://wattsupwiththat.com/2011/03/10/visualizing-the-greenhouse-effect-emission-spectra/
Petty’s book is awesome, BTW. Well worth $25. But you have to know some physics to get through parts of it and get much out of it. Other parts (in particular the pictures Glickstein reproduces) are self-explanatory and constitute direct empirical evidence for the GHE in action.

tjfolkerts
April 18, 2013 10:57 pm

There are just too many errors in the top post for me to be comfortable.
WATT: “… such as the 6c by 2050 Joe Romm claims”
No. The very link included there shows that Romm is talking about 2100, not 2050. And that 6 C is a generous estimate — the original was 5.1 C. The 2050 number was an error introduced by the reporter.
HAPPER: “… we see a graph with a 6 C temperature rise by 2050 …”
No. The article is not very clear, but the graph suggests that projections of a 6 C rise “in the long term” (which in context is pretty clearly 2100, not 2050) are possible. This projection supposes that energy demands continue to increase and that each joule of energy produced continues to require the same amount of CO2 (the so-called “carbon dependency”).
HAPPER: “The temperature change, ∆T , from the mean temperature of the present (the year 2013) … ”
While I agree with the math, I disagree with some of the numbers chosen. The original projections seem to be for a 5.1 C increase from 1990-2100 (with 6 C being a high-end estimate), when CO2 was ~ 355 ppm., By choosing to start 23 years later and 10% higher in CO2, the results are inflated. Throwing in ~ 0.2 C warming already from 1990 – 2013, the CO2 numbers become a much lower 1100 – 1400 ppm, rather than ~ 1600 ppm.
HAPPER: “But the rate of increase of CO2 has been pretty close to 2 ppm/year, which implies that by the year 2050 the CO2 concentration will be larger by about (50−13) years×2 ppm/ year … ”
First, as has been show already, the year should be 2100, not 2050. Dr Happer chose a linear increase, which would be ~ 575 ppm by 2100. The original projections choose a more exponential increase, growing to almost 900 ppm.
Projecting ahead is difficult, but projecting a continued upward trend in CO2 is certainly not outlandish. Suddenly a projected increase to ~ 900 ppm is not so far off from ~ 1200 ppm needed for the “simple model” to get to reasonable values by 2100.
(Furthermore, the original paper for the 5.1 C projection (rounded up to 6 C) (http://journals.ametsoc.org/doi/pdf/10.1175/2009JCLI2863.1) also included increases in N2O and CH4, so not all of the warming was from CO2. So really we are looking at perhaps a 4 C increase from CO2 itself.)
HAPPER: “A 6 C warming from CO2 emissions by 2050 is absurd. It is a religious slogan …”
Yes it is absurd. It is an absurd meme that apparently has become a strawman by skeptics, not a view held by even the wildest of alarmists. It is a shame that these numbers detract the other points made by Dr Happer.

Konrad
April 18, 2013 11:19 pm

rgbatduke says:
April 18, 2013 at 10:15 pm
“So, any papers, computations, models, actual evidence to support your assertion?”
———————————————————————————————————
Yes, these claims are backed by empirical experiments. I have designed simple versions so other climate bloggers can build and run them for themselves. A list was posted at WUWT here –
http://wattsupwiththat.com/2013/04/05/a-comparison-of-the-earths-climate-sensitivity-to-changes-in-the-nature-of-the-initial-forcing/#comment-1267231
Experiment 1 demonstrates that incident LWIR on the surface of liquid water does not have the same effect on cooling rate as it does on other materials.
Experiment 2 demonstrates the ability of CO2 to radiate energy it has acquired by conduction. Most of the net energy being radiated to space by radiative gases was acquired by surface conduction and the release of latent heat.
Experiment 3 demonstrates that convective circulation in fluid in a gravity field can be driven by removing energy from the top of the fluid. Radiative gases do this in our atmosphere. Adiabatic cooling of ascending air masses does not represent a loss of energy from an air mass and therefore does not create a loss of buoyancy.
Experiment 4 demonstrates two important things. First, the relative height of energy input and output for a gas column in a gravity field determines whether convective circulation develops. Secondly, in box 2 where strong convective circulation does not develop, the average gas temperature is higher. Heated gases rise to the top of box 2 and do not descend. Cooling in box 2 is limited to the speed of gas conduction. The bigger you build the experiment, the better it works (scale and speed of gas conduction issues). Heating and cooling a gas column in a gravity field at separate locations at the base results in a higher average temperature than heating at the base and cooling at the top.
Experiment 5 demonstrates the folly of treating gas as a static body when calculating surface to gas conductive flux. The two tubes cool at different rates. In tube 1 with the cling film at the top, convective circulation develops, bringing the hottest air against the cooling surface and maximising conductive flux. In tube 2 with the cling film at the base, gravity keeps the coldest gas against the cooling surface, minimising conductive flux. The same effect works in our atmosphere. Gravity moves the coldest gases against the surface during the day, maximising conductive flux into the atmosphere. Gravity moves the coldest gases against the surface at night, minimising conductive flux out of the atmosphere. This experiment also demonstrates why conductive flux between the surface and atmosphere should not be calculated from surface Tav. Land surface Tav may be lower under a non radiative atmosphere, but this does not translate to a cooler atmosphere.
Experiments 3 to 5 cover the issues raised concerning moving gases in my post above. Experiment 4 and 5 are scale dependant. The bigger you build them the better they work.
AGW calculations only show warming when you treat the atmosphere as a static body. Moving gasses are the stake through the heart of AGW.

David Cage
April 18, 2013 11:48 pm

No pay walled document should be allowed to be cited in any action involving public policy. In effect it is giving a free hand for lies and corruption if information cannot be readily checked.

Jon
April 18, 2013 11:48 pm

“Incidentally, if anyone out there can explain the alleged mechanism by which CO2 molecules “trap” heat, I’d be all ears. Somebody is having a laugh, for now
“Trap heat” or variations thereof is a phrase often used by AGW proponents. It sounds scary. But I’m not sure what it means. I’d be grateful if someone would define what is meant by “trap heat”. Does it mean “heat that can never escape, or heat that can escape but only under certain conditions”; and if so, “what are the conditions necessary for the “heat to escape”?”
A better Word could be “delay”? But Earths atmosphere is mostly water vapour and air density driven in this context. To get 6 deg warming you need more sunlight to the surface or globally more air density?

Konrad
April 18, 2013 11:50 pm

rgbatduke says:
April 18, 2013 at 10:15 pm
————————————————————————————————————–
Further to Experiment 4 above, here is a graphic of what happens in the two boxes –
http://tinypic.com/r/zmghtu/6
The following graphic shows what that means for the atmosphere –
http://i45.tinypic.com/29koww6.jpg
It should be noted that the panel on the right listed as non radiative atmosphere only shows what would happen shortly after radiative cooling was “switched off”. As Ferd Berple pointed out in a post above after this the atmosphere would go isothermal. Without radiative gases, atmospheric temperatures above the near surface layer would slowly rise to temperatures close to surface Tmax.
To observe the unusual characteristics of an atmosphere without radiative gases you only need to look at the stratosphere. Here there is no strong vertical convective circulation, the lapse rate reverses and molecular energy rapidly rises. It is also important to note that there are no planets or moons in the solar system that have managed to retain an atmosphere without radiative gases.

Roger Knights
April 19, 2013 12:07 am

David Cage says:
April 18, 2013 at 11:48 pm
No pay walled document should be allowed to be cited in any action involving public policy.

Agreed; the government or UN should buy out the copyrights on all climate-related papers and put them in the public domain.

April 19, 2013 12:13 am

Dr. Happer, I hope you’re taking questions.
I would be interested to hear your take on this:
I understand your analysis, but the major underlying assumption of the classical theory is that pure black body radiative equilibrium is the primary method of heat rejection on earth, while ignoring an important distinction.
1) With the classical analysis, one simply measures the albedo of the earth, and with known incoming radiation, we can calculate the radiative balance temperature easily. We see the difference and attribute that to the greenhouse effect. Then we add the effect of a CO2 doubling to that to see what the impact is. And then we imagine that albedo will stay the same if more water is evaporated with the higher temperature, which will result in a still higher temperature, and that is why we use a feedback that is >0. We do not assume that albedo will increase on average to reject more heat, both through cloud SW rejection, and reduction of the distance water droplet LW needs to travel to escape to space.
2) This is backwards. The albedo is an output of the system, not an input, and is not stable. It is a result or property of the atmosphere and water vapor in a given volume under different conditions. The correct approach would be to take the albedo of the earth everywhere that there are not clouds, then with the given solar input, calculate the non-cloud radiative balance using this much darker albedo. Now you have the starting conditions of a planet that has no ability to use H20 convection processes. This temperature is much higher since more LW is absorbed. Now we see the difference and attribute the difference to the effect of (1) albedo due to clouds, and (2) all other GHG’s (including water vapor). Not much left for “all other” is there?
3) Planets that are like ours but that are more distant from the sun will have fewer cloud processes than ours (less power delivered, less to reject). Planets that are closer will have more. In other words, all else being equal, a rock / water planet closer to the sun will be brighter, one more distant will be cooler and won’t require active heat rejection.
4) there is an equilibrium distance to the sun for a given baseline (rock & water) albedo at which convection begins to occur at lower latitudes. As the distance to the sun decreases, (and more power is delivered to the planet) the convection will move up the latitudes (and probably form bands), but the albedo will increase with cloud activity. Planets farther than this distance are controlled purely by the classical blackbody equilibrium equations. Planets closer are actively managed via active H20 albedo control, which flattens the temperature profile and creates temperature stability at the surface. Planets very much closer have even more stability and higher albedo. The very fact that albedo changes is indication of a very strong heat rejection mechanism. I don’t want to call it a feedback because I think the entire feedback argument suffers from this same fundamental flaw in thinking. But the fact that the system has a wide band of stability at the surface over a wide range in power input indicates a system in negative feedback control.
5) This active cooling process works in concert with, but certainly would overwhelm CO2’s tiny signature. So, as Willis points out, the effect might be earlier onset or later dissipation of a convective event. Longer duration = higher average albedo over a day. I would also add that the altitude to which water droplets are delivered so that they LW radiate out faster may increase with added CO2.
6) Combining 3,4, and 5, albedo is the system output that manages temperature when planets are close to the sun. The heat capacity of the earth can cause the albedo output to overshoot and undershoot, creating chaotic or cyclical change in temperatures. Likewise, polar regions may contain ice which both insulates LW from the oceans and reflects SW. It’s not hard to imagine a stable planet that has quite a bit of natural variation simply due to other processes kicking in that contribute to under damp the system. For example, we are seeing that after the most recent warm period, stratospheric water vapor is in decline, which is effectively shunting even more LW to space. This process may take years or decades to reverse, which could produce a long cool period before this shutter cycles back to a higher level IR blocking state, and warming would begin again. There are probably countless of these unknowns acting on the system.
7) If you buy that albedo control buys stability at the surface, this means the H20 feedback is negative.
I suspect it is also incorrect to average the 1/2 earth’s input facing the sun with the dark half radiating to space, since these have much different properties and temperatures and this is also a big problem for the classical analysis. Each grid area on earth needs to be integrated to find the values over a day and year (and on and on) for the radiative exchanges going on.
I just saw an article today that mentioned in one sentence that NASA now seems to understand this albedo difference (or at least has me convinced they have an inkling of it). This also means that the classical radiative balance theory that starts with albedo and calculates the effect of CO2 on top of it, then water vapor on top of that (which is absurd) is being abandoned by even the big pro-warmers, something even most skeptics still largely accept, just with low feedback. I’m thinking the whole feedback issue is a result of poorly defining the problem. It gives me hope that NASA might start learning something about this planet now that Hansen is gone. That the classical theory has failed is now beyond dispute, everyone is doing the climb down.
Do you think my order of looking at the problem is more correct than the classical (static albedo) view ? What flaws do you see? Any insights? THANK YOU !!!

Peter Miller
April 19, 2013 12:19 am

I suspect there is a natural law we are about to discover, which states something like: “The more observations refuse to demonstrate AGW/CAGW, the more alarming the climate model forecasts will have to become to receive ‘research’ funding.”

April 19, 2013 12:23 am

Andrew says:
April 18, 2013 at 4:45 pm
Doesn’t it get ever more difficult to increase the ppmv of CO2 in the atmosphere? CO2, as I understand it, partitions at a ration of 50:1 between water and air.

You are confusing total amounts in the oceans with the changes observed at equilibrium.
The oceans indeed contain 50 times more CO2 than the atmosphere, but that is not important. What is important is what happens when the amount of CO2 in the atmosphere increases (by whatever cause). With increased CO2 (partial) pressure in the atmosphere, according to Henry’s Law, the same increase in CO2 pressure in the ocean surface must occur to reach a new equilibrium. Thus the 30% increase over the past 1.5 century increased the free CO2 level in the oceans with 30%. So far so good and simple.
But free CO2 is only 1% of all CO2 in the oceans. Most are bicarbonates and carbonates, which don’t count as free CO2. What happens next? Somewhat more difficult: free CO2 is in chemical equilibrium with bicarbonates and carbonates, thus more CO2 gives more of the other and at the same time more hydrogen ions (that is acidity, or in this case less alkalinity). But more hydrogen ions push the equilibrium back to free CO2.
The total result is that a 30% change of CO2 in the atmosphere indeed gives a 30% change of free CO2 in the oceans surface, but only a 3% change in total dissolved CO2 (called DIC, that is free CO2 + bicarbonate + carbonate) in the oceans surface. As the oceans surface contains about 1000 GtC, the increase over the past 1.5 century was not more than 30 GtC.
Thus instead of a 50:1 ratio, the real ratio is 1:10 for the ocean surface/atmosphere partitioning.
The absorption of any CO2 increase in the deep oceans is where the bulk of CO2 change can go (together with long term capture of carbon by land plants). The difference is in timing: the equilibrium between ocean surface and atmosphere is reached in 1-3 years half life time, but the deep oceans-atmosphere exchanges are limited in flux and need much longer periods to reach equilibrium (half life time ~40 years).

Richard111
April 19, 2013 12:28 am

“”rgbatduke says:
April 18, 2013 at 10:45 pm
……
As for what proportion of the gallon-plus that is CO_2 is “man made” or attributable to humans — that is debatable,…””

That is a problem that bothers me. I read that “man made” CO2 in the atmosphere is calculated on the basis of the absence of C-14. But C-14 is continuously produced in the upper atmosphere by cosmic ray activity and there is no acknowledged level of production. So if they can’t measure C-14 production, how do the measure C-14 absence? Also current solar activity is low thus cosmic ray activity is high so it should then show a reduction in “man made” CO2.
Oh, well. Time will tell (I hope).

tokyoboy
April 19, 2013 12:42 am

For the past 20 years the Mauna Loa CO2 concentration trend is almost perfectly linear.
If, as usually postulated, a fixed fraction (ca. 50%) of anthropogenic CO2 remains in the atmosphere, a linear trend is generated ONLY WHEN THE YEARLY CO2 EMISSION IS CONSTANT THROUGHOUT.
However, we know that the emission has been increasing for those 20 years throughout, and hence the CO2 concentration curve should be superlinear.
This is an all-time enigma for me.

Martin A
April 19, 2013 1:14 am

“The proportionality of the temperature increment ∆T to ln N is widely accepted. ”
It has become climate science folklore with essentially the status of a physical law..
Everybody “knows” it is true and believes it – even global warming skeptics. Yet tracking down its origin is difficult – it seems to have originated by fitting a log formula to some numerical results from a radiative forcing model, not from the analytical solution of a physical model.

tokyoboy
April 19, 2013 1:28 am

“Martin A says: April 19, 2013 at 1:14 am ……”
I guess the ∆T ~ ln C is an empirical formula from the fact that the 15-micron O2 band is practically saturated at the peak, and hence the additional CO2 causes essentially slow band broadening, which is approximated by the ∆T ~ ln C formula.

Andrew
April 19, 2013 1:29 am

LdB Konrad
LdB says: “… it may be hard to explain using classic physics and people with only that level of science may struggle understanding but the ridiculous comments that people “want to be shown how CO2 traps in heat” should be attacked for the science ignorance they show.”
I’ll tell you what “science ignorance” is LdB, it is having the notion in your head that a greenhouse and a greenhouse without a roof aren’t different.
Konrad “gets it”, as do many other contributors here. The “science ignorance” is not helped by widespread, lazy and slack terminology. CO2, which doesn’t change state, is called a ‘greenhouse gas’ along with the heavy lifter in the heat transport and surface cooling business, namely water, which does change state. Heat transfers in the atmosphere involving the water cycle utterly dwarf any possible contribution from CO2, if that were even +ve, and if it could be measured. Tell you what – I’ll replace all those air gaps in your double glazing with your super heating agent, CO2, at the special “science ignorance” price of only $10,000.

richard telford
April 19, 2013 1:32 am

Happer seems to be the only person estimating how much CO2 is needed to get a 6C rise from 2013 concentrations of ~400ppm rather than pre-industrial concentrations of ~270ppm. This makes a substantial difference in the answer (1600 vs 1080ppm).
In assuming that CO2 concentrations will continue to rise at 2ppm/yr, he is making some very strong assumptions about future emission scenarios. Without strong intervention, it is much more likely that the increase in CO2 concentrations per year will continue to rise (tokyoboy April 19, 2013 at 12:42 am – don’t just eyeball the data, calculate the slope – it is superlinear).
The Happer argues that a climate sensitivity of 1C per doubling is more plausible. This is a fantasy not supported by the empirical evidence. Nic Lewis’s paper had a modal sensitivity of 1.6C. Happer’s suggestion that climate sensitivity might be negative is a joke. If he really thought this plausible, it should scare him, as increasing CO2 concentrations would cool the planet! Has he really thought this through?

TerryS
April 19, 2013 1:32 am

Re: joelshore

(1) The entire argument being attacked is essentially a “strawman” since in the very article of Joe Romm’s that Anthony linked to, Romm says he was talking about a 6C rise by 2100, not 2050.

The argument he presents still holds for 2100. At 2ppm/year you get a CO2 concentration of 574, still much less that the required 1600ppm (630ppm with accelerating rate of CO2).

(2) He assumes that CO2 levels will continue rising at their current rate of 2 ppm per year. However, historically, the rate of increase of CO2 has been accelerating over time: 40 years ago, it was rising at only about 1 ppm per year ( http://wonkroom.thinkprogress.org/wp-content/uploads/2009/03/co2_growth_rate.PNG ). Hence, it is unlikely that 40 years from now it will still be rising at 2 ppm per year, especially under assumptions of no constraints on CO2 emissions. And, if the rate of rise keeps doubling every 40 years, it will be going up ~8 ppm per year by the end of the 21st century.

The rate of increase of CO2 is expected to accelerate as countries like China and India industrialise, however, it isn’t expected to be exponential (that would require industrialisation rates to be exponential). If we take a linear acceleration of 1ppm/40 years then it would still take 240 years to reach the 1600ppm in the article.

(3) He computes the necessary CO2 level for a 6 C rise from current temperatures (i.e., that with a 3 C sensitivity, one has to quadruple CO2 from 400 ppm to 1600 ppm). If we talk about from pre-industrial levels, a quadrupling of CO2 only means going up to ~1100 ppm.

The CO2 sensitivity is irrespective of the starting point. If the sensitivity is 3C then doubling CO2 from today’s levels would still result in a 3C rise. His computation using today’s CO2 levels and temperature is just as valid and accurate as using CO2 and temperature levels from 150 years ago.
To get to ~1100 at 2ppm/year would still require 355 years, or, with an accelerating CO2 increase 171 years.
As for the accelerating rate of CO2, do you seriously believe that it will take China, India etc anywhere near a 100 years to industrialise? Once they have industrialised their CO2 emissions should level off (they same way they have in the industrialised nations).