The Cold Equations

Guest Post by Willis Eschenbach

I’ve tried writing this piece several times already. I’ll give it another shot, I haven’t been happy with my previous efforts. It is an important subject that I want to get right. The title comes from a 1954 science fiction story that I read when I was maybe ten or eleven years old. The story goes something like this:

A girl stows away on an emergency space pod taking anti-plague medicine to some planetary colonists. She is discovered after the mother ship has left. Unfortunately, the cold equations show that the pod doesn’t have enough fuel to land with her weight on board, and if they dump the medicine to lighten the ship the whole colony will perish … so she has to be jettisoned through the air lock to die in space.

I was hugely impressed by the story. I liked math in any case, and this was the first time that I saw how equations can provide us with undeniable and unalterable results. And I saw that the equations about available fuel and weight weren’t affected by human emotions, they either were or weren’t true, regardless of how I or anyone might feel about it.

Lately I’ve been looking at the equations used by the AGW scientists and by their models. Figure 1 shows the most fundamental climate equation, which is almost tautologically true:

Figure 1. The most basic climate equation says that energy in equals energy out plus energy going into the ocean. Q is the sum of the energy entering the system over some time period. dH/dt is the change in ocean heat storage from the beginning to the end of the time period. E + dH/dt is the sum of the outgoing energy over the same time period. Units in all cases are zettajoules (ZJ, or 10^21 joules) / year.

This is the same relationship that we see in economics, where what I make in one year (Q in our example) equals what I spend in that year (E) plus the year-over-year change in my savings (dH/dt).

However, from there we set sail on uncharted waters …

I will take my text from HEAT CAPACITY, TIME CONSTANT, AND SENSITIVITY OF EARTH’S CLIMATE SYSTEM, Stephen E. Schwartz, June 2007 (hereinafter (S2007). The study is widely accepted, being cited 193 times. Here’s what the study says, inter alia (emphasis mine).

Earth’s climate system consists of a very close radiative balance between absorbed shortwave (solar) radiation Q and longwave (thermal infrared) radiation emitted at the top of the atmosphere E.

Q ≈ E                                                                       (1)

The global and annual mean absorbed shortwave irradiance Q  = γ J, where γ [gamma] is the mean planetary coalbedo (complement of albedo) and J is the mean solar irradiance at the top of the atmosphere (1/4 the Solar constant) ≈ 343 W m-2. Satellite measurements yield Q ≈ 237 W m-2 [Ramanathan 1987; Kiehl and Trenberth, 1997], corresponding to γ ≈ 0.69. The global and annual mean emitted longwave irradiance may be related to the global and annual mean surface temperature GMST Ts as E = ε σ Ts^4 where ε (epsilon) is the effective planetary longwave emissivity, defined as the ratio of global mean longwave flux emitted at the top of the atmosphere to that calculated by the Stefan-Boltzmann equation at the global mean surface temperature; σ (sigma) is the Stefan-Boltzmann constant.

Within this single-compartment energy balance model [e.g., North et al., 1981; Dickinson, 1982; Hansen et al., 1985; Harvey, 2000; Andreae et al., 2005, Boer et al., 2007] an energy imbalance Q − E arising from a secular perturbation in Q or E results in a rate of change of the global heat content given by

dH/dt = Q – E                                                               (2)

where dH/dt is the change in heat content of the climate system.

Hmmm … I always get nervous when someone tries to slip an un-numbered equation into a paper … but I digress. Their Equation (2) is the same as my Figure 1 above, which was encouraging since I’d drawn Figure 1 before reading S2007. S2007 goes on to say (emphasis mine):

The Ansatz of the energy balance model is that dH/dt may be related to the change in GMST [global mean surface temperature] as

dH/dt = C dTs/dt                          (3)

where C is the pertinent heat capacity. Here it must be stressed that C is an effective heat capacity that reflects only that portion of the global heat capacity that is coupled to the perturbation on the time scale of the perturbation. In the present context of global climate change induced by changes in atmospheric composition on the decade to century time scale the pertinent heat capacity is that which is subject to change in heat content on such time scales. Measurements of ocean heat content over the past 50 years indicate that this heat capacity is dominated by the heat capacity of the upper layers of the world ocean [Levitus et al., 2005].

In other words (neglecting the co-albedo for our current purposes), they are proposing two substitutions in the equation shown in Figure 1. They are saying that

E = ε σ Ts^4

and that

dH/dt = C dTs/dt

which gives them

Q = ε σ Ts^4 + C dTs/dt                     (4)

Figure 2 shows these two substitutions:

Figure 2. A graphic view of the two underlying substitutions done in the “single-compartment energy balance model” theoretical climate explanation. Original equation before substitution is shown in light brown at the lower left, with the equation after substitution below it.

Why are these substitutions important? Note that in Equation (4), as shown in Figure 2, there are only two variables — radiation and surface temperature. If their substitutions are valid, this means that a radiation imbalance can only be rectified by increasing temperature. Or as Dr. Andrew Lacis of NASA GISS recently put it (emphasis mine):

As I have stated earlier, global warming is a cause and effect problem in physics that is firmly based on accurate measurement and well established physical processes. In particular, the climate of Earth is the result of energy balance between incoming solar radiation and outgoing thermal radiation, which, measured at the top of the atmosphere, is strictly a radiative energy balance problem. Since radiative transfer is a well established and well understood physics process, we have accurate knowledge of what is happening to the global energy balance of Earth. And as I noted earlier, conservation of energy leaves no other choice for the global equilibrium temperature of the Earth but to increase in response to the increase in atmospheric CO2.

Dr. Lacis’ comments are an English language exposition of the S2007 Equation (4) above. His statements rest on Equation (4). If Equation (4) is not true, then his claim is not true. And Dr. Lacis’ claim, that increasing GHG forcing can only be balanced by a temperature rise, is central to mainstream AGW climate science.

In addition, there’s a second reason that their substitutions are important. In the original equation, there are three variables — Q, E, and H. But since there are only two variables (Ts and Q) in the S2007 version of the equation, you can solve for one in terms of the other. This allows them to calculate the evolution of the surface temperature, given estimates of the future forcing … or in other words, to model the future climate.

So, being a naturally suspicious fellow, I was very curious about these two substitutions. I was particularly curious because if either substitution is wrong, then their whole house of cards collapses. Their claim, that a radiation imbalance can only be rectified by increasing temperature, can’t stand unless both substitutions are valid.

SUBSTITUTION 1

Let me start with the substitution described in Equation (3):

dH/dt = C dTs/dt                          (3)

The first thing that stood out for me was their description of Equation (3) as “the Ansatz of the energy balance model”.

“And what”, sez I, “is an ‘Ansatz’ when it’s at home?” I’m a self-educated reformed cowboy, it’s true, but a very well-read reformed cowboy, and I never heard of the Ansatz.

So I go to Wolfram’s Mathworld, the internet’s very best math resource, where I find:

Ansatz

An ansatz is an assumed form for a mathematical statement that is not based on any underlying theory or principle.

Now, that’s got to give you a warm, secure feeling. This critical equation, this substitution of the temperature change as a proxy for the ocean heat content change, upon which rests the entire multi-billion-dollar claim that increased GHGs will inevitably and inexorably increase the temperature, is described by an enthusiastic AGW adherent as “not based on any underlying theory or principle”. Remember that if either substitution goes down, the whole “if GHG forcings change, temperature must follow” claim goes down … and for this one they don’t even offer a justification or a citation, it’s merely an Ansatz.

That’s a good thing to know, and should likely receive wider publication …

It put me in mind of the old joke about “How many legs does a cow have if you call a tail a leg?”

“Four, because calling a tail a leg doesn’t make it a leg.”

In the same way, saying that the change oceanic heat content (dH/dt) is some linear transformation of the change in surface temperature (C dTs/dt) doesn’t make it so.

In fact, on an annual level the correlation between annual dH/dt and dTs/dt is not statistically significant (r^2=0.04, p=0.13). In addition, the distributions of dH/dt and dTs/dt are quite different, both at a quarterly and an annual level. See Appendix 1 and 4 for details. So no, we don’t have any observational evidence that their substitution is valid. Quite the opposite, there is little correlation between dH/dt and dTs/dt.

There is a third and more subtle problem with comparing dH/dt and dTs/dt. This is that H (ocean heat content) is a different kind of animal from the other three variables Q (incoming radiation), E (outgoing radiation), and Ts (global mean surface air temperature). The difference is that H is a quantity and Q, E, and Ts are flows.

Since Ts is a flow, it can be converted from the units of Kelvins (or degrees C) to the units of watts/square metre (W/m2) using the blackbody relationship σ Ts^4.

And since the time derivative of the quantity H is a flow, dH/dt, we can (for example) compare E + dH/dt to Q, as shown in Figure 1. We can do this because we are comparing flows to flows. But they want to substitute a change in a flow (dT/dt) for a flow (dH/dt). While that is possible, it requires special circumstances.

Now, the change in heat content can be related to the change in temperature in one particular situation. This is where something is being warmed or cooled through a temperature difference between the object and the surrounding atmosphere. For example, when you put something in a refrigerator, it cools based on the difference between the temperature of the object and the temperature of the air in the refrigerator. Eventually, the object in the refrigerator takes up the temperature of the refrigerator air. And as a result, the change in temperature of the object is a function of the difference in temperature between the object and the surrounding air. So if the refrigerator air temperature were changing, you could make a case that dH/dt would be related to dT/dt.

But is that happening in this situation? Let’s have a show of hands of those who believe that as in a refrigerator, the temperature of the air over the ocean is what is driving the changes in ocean heat content … because I sure don’t believe that. I think that’s 100% backwards. However, Schwartz seems to believe that, as he says in discussing the time constant:

… where C’ is the heat capacity of the deep ocean, dH’/dt is the rate of increase of the heat content in this reservoir, and ∆T is the temperature increase driving that heat transfer.

In addition to the improbability of changes in air temperature driving the changes in ocean heat content, the size of the changes in ocean heat content also argues against it. From 1955 to 2005, the ocean heat content changed by about 90 zettajoules. It also changed by about 90 zettajoules from one quarter to the next in 1983 … so the idea that the temperature changes (dT/dt) could be driving (and thus limiting) the changes in ocean heat content seems very unlikely.

Summary of Issues with Substitution 1:   dH/dt = C dT/dt

1. The people who believe in the theory offer no theoretical or practical basis for the substitution.

2. The annual correlation of dH/dt and dT/dt is very small and not statistically significant.

3. Since H is a quantity and T is a flow, there is no a priori reason to assume a linear relationship between the two.

4. The difference in the distributions of the two datasets dH/dt and dT/dt (see Appendix 1 and 4) shows that neither ocean warming nor ocean cooling are related to dT/dt.

5. The substitution implies that air temperature is “driving that heat transfer”, in Schwartz’s words. It seems improbable that the wisp of atmospheric mass is driving the massive oceanic heat transfer changes.

6. The large size of the quarterly heat content changes indicates that the heat content changes are not limited by the corresponding temperature changes.

My conclusion from that summary? The substitution of C dT/dt for dH/dt is not justified by either observations or theory. While it is exceedingly tempting to use it because it allows the solution of the equation for the temperature, you can’t make a substitution just because you really need it in order to solve the equation.

SUBSTITUTION 2: E = ε σ Ts^4

This is the sub rosa substitution, the one without a number. Regarding this one, Schwartz says:

The global and annual mean emitted longwave irradiance may be related to the global and annual mean surface temperature GMST Ts as

E = ε σ Ts^4

where ε (epsilon) is the effective planetary longwave emissivity, defined as the ratio of global mean longwave flux emitted at the top of the atmosphere [TOA] to that calculated by the Stefan-Boltzmann equation at the global mean surface temperature; σ (sigma) is the Stefan-Boltzmann constant.

Let’s unpick this one a little and see what they have done here. It is an alluring idea, in part because it looks like the standard Stefan-Boltzmann equation … except that they have re-defined epsilon ε as “effective planetary emissivity”. Let’s follow their logic.

First, in their equation, E is the top of atmosphere longwave flux, which I will indicate as Etoa to distinguish it from surface flux Esurf. Next, they say that epsilon ε is the long-term average top-of-atmosphere (TOA) longwave flux [ which I’ll call Avg(Etoa) ] divided by the long-term average surface blackbody longwave flux [ Avg(Esurf) ]. In other words:

ε = Avg(Etoa) /Avg(Esurf)

Finally, the surface blackbody longwave flux Esurf is given by Stefan-Boltzmann as

Esurf = σ Ts^4.

Substituting these into their un-numbered Equation (?) gives us

Etoa = Avg(Etoa) / Avg(Esurf) * Esurf

But this leads us to

Etoa / Esurf = Avg(Etoa) / Avg(Esurf)

which clearly is not true in general for any given year, and which is only true for long-term averages. But for long-term averages, this reduces to the meaningless identity Avg(x) / Avg(anything) = Avg(x) / Avg(anything).

Summary of Substitution 2: E = ε σ Ts^4

This substitution is, quite demonstrably, either mathematically wrong or meaninglessly true as an identity. The cold equations don’t allow that kind of substitution, even to save the girl from being jettisoned. Top of atmosphere emissions are not related to surface temperatures in the manner they claim.

My conclusions, in no particular order:

• Obviously, I think I have shown that neither substitution can be justified, either by theory, by mathematics, or by observations.

• Falsifying either one of their two substitutions in the original equation has far-reaching implications.

• At a minimum, falsifying either substitution means that in addition to Q and Ts, there is at least one other variable in the equation. This means that the equation cannot be directly solved for Ts. And this, of course, means that the future evolution of the planetary temperature cannot be calculated using just the forcing.

• In response to my posting about the linearity of the GISS model, Paul_K pointed out the Schwartz S2007 paper. He also showed that the GISS climate model slavishly follows the simple equations in the S2007 paper. Falsifying the substitutions thus means that the GISS climate model (and the S2007 equations) are seen to be exercises in parameter fitting. Yes, they can can give an approximation of reality … but that is from the optimized fitting of parameters, not from a proper theoretical foundation.

• Falsifying either substitution means that restoring radiation balance is not a simple function of surface temperature Ts. This means that there are more ways to restore the radiation balance in heaven and earth than are dreamt of in your philosophy, Dr. Lacis …

As always, I put this up here in front of Mordor’s unblinking Eye of the Internet to encourage people to point out my errors. That’s science. Please point them out with gentility and decorum towards myself and others, and avoid speculating on my or anyone’s motives or honesty. That’s science as well.

w.

Appendix 1: Distributions of dH/dt and dT/dt

There are several ways we can see if their substitution of C dT/dt for dH/dt makes sense and is valid. I usually start by comparing distributions. This is because a linear relationship, such as is proposed in their substitution, cannot change the shape of a distribution. (I use violinplots of this kind of data because they show the structure of the dataset. See Appendix 2 below for violinplots of common distributions.)

A linear transformation can make the violinplot of the distribution taller or shorter, and it can move the distribution vertically. (A negative relationship can also invert the distribution about a horizontal axis, but they are asserting a positive relationship).But there is no linear transformation (of the type y = m x + b) that can change the shape of the distribution. The “m x” term changes the height of the violinplot, and the “b” term moves it vertically. But a linear transformation can’t change one shape into a different shape.

First, a bit of simplification. The “” operator indicates “change since time X”. We only have data back to 1955 for ocean heat content. Since the choice of “X” is arbitrary, for this analysis we can say that e.g. ∆T is shorthand for T(t) – T(1955). But for the differentiation operation, this makes no difference, because the T(1955) figure is a constant that drops out of the differentiation. So we are actually comparing dH/dt(annual change in ocean heat content) with C dT/dt (annual change in temperature)

Figure 2 compares the distributions of dH/dt and dT/dt. Figure A1 shows the yearly change in the heat content H (dH/dt) and the yearly change in the temperature T (dT/dt).

Figure A1 Violinplot comparison of the annual changes in ocean heat content dH/dt and annual changes in global surface temperature dT/dt. Width of the violinplot is proportional to the number of observations at that value (density plot). The central black box is a boxplot, which covers the interquartile range (half of the data are within that range). The white dot shows the median value.

In addition to letting us compare the shapes, looking at the distribution lets us side-step all problems with the exact alignment of the data. Alignment can present difficulties, especially when we are comparing a quantity (heat content) and a flow (temperature or forcing). Comparing the distributions avoids all these alignment issues.

With that in mind, what we see in Figure A1 doesn’t look good at all. We are looking for a positive linear correlation between the two datasets, but the shapes are all wrong. For a linear correlation to work, the two distributions have to be of the same shape. But these are of very different shapes.

What do the shapes of these violinplots show?

For the ocean heat content changes, the peak density at ~ – 6 ZJ shows that overall the most common year-to-year change is a slight cooling. When warming occurs, however, it tends to be larger than the cooling. The broad top of the violinplot means that there are an excess of big upwards jumps in ocean heat content.

For the temperature changes, the reverse is true. The most common change is a slight warming of about 0.07°C. There are few examples of large warmings, whereas large coolings are more common. So there will be great difficulties equating a linear transform of the datasets.

The dimensions of the problem become more apparent when we look at the distributions of the increases (in heat content or temperature) versus the distributions of the decreases in the corresponding variables. Figure A2 compares those distributions:

Figure A2. Comparison of the distribution of the increases (upper two panels) and the decreases (lower two panels) in annual heat content and temperature. “Equal-area” violinplots are used.

Here the differences between the two datasets are seen to be even more pronounced. The most visible difference is between the increases. Many of the annual increases of the ocean heat content are large, with a quarter of them more than 20 ZJ/yr and a broad interquartile range (black box, which shows the range of the central half of the data). On the other hand, there are few large increases of the temperature, mostly outliers beyond the upper “whisker” of the boxplot.

The reverse is also true, with most of the heat content decreases being small compared to the corresponding temperature decreases. Remember that a linear transformation such as they propose, of the form (y = m x + b), has to work for both the increases and the decreases … which in this case is looking extremely doubtful.

My interpretation of Figure A2 is as follows. The warming and cooling of the atmosphere is governed by a number of processes that take place throughout the body of the atmosphere (e.g. longwave radiation absorption and emission, shortwave absorption, vertical convection, condensation, polewards advection). The average of these in the warming and cooling directions are not too dissimilar.

The ocean, on the other hand, can only cool by releasing heat from the upper surface. This is a process that has some kind of average value around -8 ZJ/year. The short box of the boxplot (encompassing the central half of data points) shows that the decreases in ocean heat content are clustered around that value.

Unlike the slow ocean cooling, the ocean can warm quickly through the deep penetration of sunlight into the mixed layer. This allows the ocean to warm much more rapidly than it is able to cool. This is why there are an excess of large increases in ocean heat content.

And this difference in the rates of ocean warming and cooling is the fatal flaw in their claim. The different distributions for ocean warming and ocean cooling indicate to me that they are driven by different mechanisms. The Equation (3) substitution seen in S2007 would mean that the ocean warming and cooling can be represented solely by the proxy of changes in surface temperature.

But the data indicates the ocean is warming and cooling without much regard to the change in temperature. The most likely source of this is from sunlight deeply heating the mixed layer. Notice the large number of ocean heat increases greater than 20 ZJ/year, as compared to the scarcity of similarly sized heat losses. The observations show that this (presumably) direct deep solar warming both a) is not a function of the surface temperature, and b) does not affect the surface temperature much. The distributions show that the heat is going into the ocean quickly in chunks, and coming out more slowly and regularly over time.

In summary, the large differences between the distributions of dH/dt and dT/dt, combined with the small statistical correlation between the two, argue strongly against the validity of the substitution.

Appendix 2: Violinplots

I use violinplots extensively because they reveal a lot about the distribution of a dataset. They are a combination of a density plot and a box plot. Figure A3 shows the violin plots and the corresponding simple boxplots for several common distributions.

Figure A3. Violin plots and boxplots. Each plot shows the distribution of 20,000 random numbers generated using the stated distribution. “Normal>0” is a set comprised all of the positive datapoints in the adjacent “Normal” dataset.

Because the violin plot is a density function it “rounds the corners” on the Uniform distribution, as well as the bottoms of the Normal>0 and the Zipf distributions. Note that the distinct shape of the Zipf distribution makes it easy to distinguish from the others.

Appendix 3: The Zipf Distribution

Figure A3. Violinplot of the Zipf distribution for N= 70, s = 0.3. Y-axis labels are nominal values.

The distinguishing characteristics of the Zipf distribution, from the top of Figure A3 down, are:

• An excess of extreme data points, shown in the widened upper tip of the violinplot.

• A “necked down” or at least parallel area below that, where there is little or no data.

• A widely flared low base which has maximum flare not far from the bottom.

• A short lower “whisker” on the boxplot (the black line extending below the blue interquartile box) that extends to the base of the violinplot

• An upper whisker on the boxplot which terminates below the necked down area.

Appendix 4: Quarterly Data

The issue is, can the change in temperature be used as a proxy for the change in ocean heat content? We can look at this question in greater detail, because we have quarterly data from Levitus. We can compare that quarterly heat content data to quarterly GISSTEMP data. Remember that the annual data shown in Figures A1 and A2 are merely annual averages of the quarterly data shown below in Figures A4 and A5. Figure A4 shows the distributions of those two quarterly datasets, and lets us investigate the effects of averaging on distributions:

Figure A4. Comparison of the distribution of the changes in the respective quarterly datasets.

The shape of the distribution of the heat content is interesting. I’m always glad to see that funny kind of shape, what I call a “manta ray” shape, it tells me I’m looking at real data. What you see there is what can be described as a “double Zipf distribution”.

The Zipf distribution is a very common distribution in nature. It is characterized by having a few really, really large excursions from the mean. It is the Zipf distribution that gives rise to the term “Noah Effect”, where the largest in a series of natural events (say floods) is often much, much larger than the rest, and much larger than a normal distribution would allow. Violinplots clearly display this difference in distribution shape, as can be seen in the bottom part of the heat content violinplot (blue) in Figure A4. Appendix 3 shows an example of an actual Zipf distribution with a discussion of the distinguishing features (also shown in Appendix 2):

The “double” nature of the Zipf distribution I commented on above can be seen when we examine the quarterly increases in heat and temperature versus the decreases in heat and temperature, as shown in Figure A5:

Figure A5. Comparison of the distribution of the increases (upper two panels) and the decreases (lower two panels) in quarterly heat content (blue) and quarterly temperature (green)

The heat content data (blue) for both the increases and decreases shows the typical characteristics of a Zipf distribution, including the widened peak, the “necking” below the peak, and the flared base. The lower left panel shows a classic Zipf distribution (in an inverted form).

What do the distributions of the upward and downward movements of the variables in Figure A5 show us? Here again we see the problem we saw in the annual distributions. The distributions for heat content changes are Zipf distributions, and are quite different in shape from the distributions of the temperature changes. Among other differences, the inter-quartile boxes of the boxplots show that the ocean heat content change data is much more centralized than the temperature change data.

In addition, the up- and down- distributions for the temperature changes are at least similar in shape, whereas the shapes of the up- and down- heat content change distributions are quite dissimilar. This difference in the upper and lower distributions is what creates the “manta-ray” shape shown in Figure A4. And the correlation is even worse than with the annual data, that is to say none.

So, as with the annual data, the underlying quarterly data leads us to the same conclusion: there’s no way that we can use dT/dt as a proxy for dH/dt.

Appendix 5: Units

We have a choice in discussing these matters. We can use watts per square metre (W m-2). The forcings (per IPCC) have a change since 1955 of around +1.75 W/m2.

We can also use megaJoules per square metre per year (MJ m-2 y-1). The conversion is:

1 watt per square metre (W m-2) = 1 joule/second per square metre (J sec-1 m-2) times 31.6E6 seconds / year = 31.6 MJ per square metre per year (MJ m-2 yr-1). Changes in forcing since 1955 are about +54 MJ per square metre per year.

Finally, we can use zettaJoules (ZJ, 10^21 joules) per year for the entire globe. The conversion there is

1 W/m2 = 1 joule/second per square metre (J sec-1 m-2) times 31.6E6 seconds / year times 5.11E14 square metres/globe = 16.13 ZJ per year (ZJ yr-1). Changes in forcing since 1955 are about +27 ZJ per year. I have used zettaJoules per year in this analysis, but any unit will do.

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MikeW
January 28, 2011 10:43 am

The cold Internet bestows immortality to all things it touches, even to little girl who meets a fate she didn’t deserve.
http://www.spacewesterns.com/articles/105/
I’d not read that story before, thanks. A powerful story with a very nostalgic flavor of the post WWII era Sci-Fi style.

Dishman
January 28, 2011 10:48 am

I believe Substitution 1 is demonstrably incorrect, from the physics.
A more correct substitution would be the temperature of Tropopause. The first problem with working there is that Tropopause is not a fixed surface.
Makarieva et al [2010] kinda starts down the road to deriving the correct substitution, but, to my read, stops well short.
If nothing else, I’ll write it up myself when I run out of bigger fish to fry.

cal
January 28, 2011 10:56 am

oeman50 says:
January 28, 2011 at 7:46 am
When I refreshed myself on Stefan-Boltzmann, my reference (Wikipedia – I know: http://en.wikipedia.org/wiki/Stefan%E2%80%93Boltzmann_law) indicated it is a description of the energy flux density. Cal says:
“I think this is a mistake. Temperature is not a flow. It is not “converted” to a power by multiplying by sigma. The output of the equation is a power density because sigma has the dimensions of Wm^2K^4.”
The equation does not attempt to make temperature a flow, it is simply a mathematical relationship describing how the energy flux density changes with temperature. And by definition, a “flux” decribes a flow, there is no flux without a flow of energy.
I think you missed my point. Willis was saying that dT/dt was a rate of change of flow. It is not.
My guess is that the original writers were saying that the energy in the sea is proportional to temperature. The proportionality is the thermal capacity. It is not an equation that is designed to explain why or how the sea warms it is simply a statement of how thermal capacity is defined.

FrankK
January 28, 2011 10:57 am

Willis,
Reading a little further regarding dH/dt = C dT/dt
In groundwater hydrology (equivalent to Heat Theory)
dV/dt = S dh/dt This is an valid equation where V is the change in volume (also eq Heat); S is the Storativity (eq heat capacity) h is the hydraulic head (eq Temperature) and t is time.
I think what you are objecting to is not the validity of that equation per se but the substitution of the surface temperature Ts for the ocean temperature which you indicate are not related. Is that correct ?

dwb
January 28, 2011 11:12 am

well, but what about heat exchange with the earth’s crust too, not just the oceans? is there some reason to discount the effects of steam vents, volcanoes, and the like?

P. Solar
January 28, 2011 11:21 am

>>
wrt to the Sub-rosa equation:
Ts is a mean. The mean of a fourth power is decidedly not the fourth power of the mean. ( two readings, 1,3 mean = 2 fourth power of mean=16; 4th powers 1 and 81; mean of fourth powers = 41) This expression is not valid.
>>
but the global temperature is not going to triple (unless Hansen turns out to be correct 😉 ) so what it the error in say comparing 300K to 310K (0C=273K)
the difference of the forth powers is about 14% whereas the diff in temp is around 3%.
So it is not negligible but not an order of magnitude off.
Maybe a important error is the lack of account for heat coming from the interior of the Earth that was mentioned above.
It seems however that Schwanz 2007 was only a first attempt at a ball park empirical figure. It is not the corner stone of AGW.
At least someone is trying to use data rather than computer models.
It all goes to underline how grossly over-simplified all this work is and just how much climate science is in its infancy. Nothing you’d want to trust to redesign life on Earth of start screwing around with geo-engineering.

stephen richards
January 28, 2011 11:23 am

random kinetic energy of
Lazy teenager has discovered a new form of energy. Even Newton missed that one.

Gunnar Strandell
January 28, 2011 11:27 am

Thank you Willis,
The term “Ansatz” is spelled Ansats in Swedish and hav some interesting explanations
in the dictionary of the Swedish Academy, that selects Nobel Prize winners in litterature:
http://g3.spraakdata.gu.se/saob/
freely translated by me:
2) attack on the enemy
7) start of something
8) impulse, initiative, idea
10) the lips position before you blow the horn
Nevertheless your article has given light to my sense of AGW being built on a vicious circle.

Graham Green
January 28, 2011 11:27 am

You must have been raised eating magic beans ol’ cowboy.
This post represents a triumph in clarity of thought.
Ansatz is defined by Google as ‘an educated guess that will be verified later’. Ansatz science from ersatz ‘scientists’.

January 28, 2011 11:34 am

Willis, what “cal” says at January 28, 2011 at 3:38 am, holds for me. Temperature is not a flow.
I think you are on to something here, but I cannot determine exactly what because of several problems.
First, it is standard procedure to identify each and every term in every equation, with that term’s appropriate physical units. For example, it is not clear what “Ts” is. Usually, T with a subscript is a temperature of some sort, with the subscript designating what location has that temperature. Of course, temperature has units of F, or R, or C, or K (Fahrenheit, Rankine, Celsius, or Kelvin, respectively). I had assumed Ts is the surface temperature of the Earth, until I read that Ts is a flow.
Second, the appropriate equation for heat flow, Q, related to heat capacity is
Q = m x Cp x (T2 – T1); where
Q is heat flow in Btu/hour (or similar heat per time units),
m is the mass, in pounds
Cp is the heat capacity constant, expressed in Btu/hr/pound/degree F,
T1 is temperature of the mass at its initial condition, in degrees F,
T2 is the temperature of the mass at its final condition, in degrees F.
It should be noted that Cp is not truly a constant, but has a slight dependence upon temperature. However, for temperatures that vary over a small range, Cp can be considered a constant.
Only by clarifying the exact units of each term may the reader follow the unit conversions and thus determine the validity of the exercise and thus the conclusions.

FrankK
January 28, 2011 11:59 am

Its a little early here so a correction I posted before is required:
I wrote:
“Willis,
Reading a little further regarding dH/dt = C dT/dt
In groundwater hydrology (equivalent to Heat Theory)
dV/dt = S dh/dt This is an valid equation where V is the change in volume (also eq Heat); S is the Storativity (eq heat capacity) h is the hydraulic head (eq Temperature) and t is time.
I think what you are objecting to is not the validity of that equation per se but the substitution of the surface temperature Ts for the ocean temperature which you indicate are not related. Is that correct ?”
===================================================
The above should read: where dV/dt is the change in volume with respect to time.
While I’m here. In groundwater hydrology (as in heat theory)
Inflow volume-Outflow volume = Change in Volume (1)
(i.e. theMass Balance equation). Dividing each side by dt
Inflow Rate – Outflow rate = dV/dt = S dh/dt (2)
This is the basis for S2007
From (2) above in heat theory therefore :
Q (rate) -E (rate) = C dT/dt (3)
This is a basic physically correct equation. The point is how this equation is interpreted is the critical issue and as you suggest what substitutions are used.
Thought provoking Willis and its getting me more interested in digging deeper
into whole basis of AGW “theory”.

FrankK
January 28, 2011 12:04 pm

Oh incidentally
Only when S dh/dt is zero in GW hydrology is the system at steady state or the heat flow equation Q=E

jae
January 28, 2011 12:08 pm

Great post, as usual!
One very minor point. You say:
“If their substitutions are valid, this means that a radiation imbalance can only be rectified by increasing temperature. Or as Dr. Andrew Lacis of NASA GISS recently put it (emphasis mine):”
Don’t you mean “…can only be rectified by increasing OR DECREASING temperature.” ? (apologies if someone else mentioned this; I don’t have time to read all the comments).

Juice
January 28, 2011 12:09 pm

I don’t know what the fuss is about. I can’t see anything wrong with the general relationship of:
dH/dt = C dT/dt
The rate of change of temperature must be linear with the rate of change in heat, proportional to the heat capacity. For real systems, the relationship might not be entirely linear, but pretty close. You might have some boundary issues depending on the thermal conductivity of the system, but generally speaking I can’t find a problem with the above relation, although it is oversimplified.
This may be interesting:
http://en.wikiversity.org/wiki/Nonlinear_finite_elements/Linear_heat_equation

Fernando
January 28, 2011 12:13 pm

dV/dt = S dh/dt
Closed cycle,
dV/dt = 0,0000000
http://sealevel.colorado.edu/current/sl_noib_global_sm.jpg
S # 0,00000
…dh/dt = 0,000000
delta (MSL mm) = 50 mm or 40 mm

Laurie Bowen
January 28, 2011 12:36 pm

Mr. Eschenbach you say . .
. . . “whole colony will perish … so she has to be jettisoned through the air lock to die in space.”
I say,
I guess I am “witarted” as I don’t understand why this is relevant . . . as it is a partial information story . . .
Mr. Eschenbach you say . .
most basic climate equation says that energy in equals energy out plus energy going into the ocean.
I say,
This I understand . . . because you said “basic”
Mr. Eschenbach you say . .
This is the same relationship that we see in economics, where what I make in one year (Q in our example) equals what I spend in that year (E) plus the year-over-year change in my savings (dH/dt).
I say,
true . . . . unless you are going in debt . . .
which leads me to that old accounting trick called. . . . 9, 8, 7, 6, + 5 = 11
as a math guy you should know it. . . if not, to understand the error . . . it must be demonstrated.
I am at the point that maybe I should just “jettison” myself from these discussions. The entire concept of understanding climate change is fairly simple to me . . . the big arguments are quantifications. . . but I need to understand the relevence of arguing about say 1000 when your dealing with 1,000,000,0000,000,000,000 . . . . with very few exceptions. I guess it takes more that a few trees for a forest to be made. . . . and of course that leads to talking about angles and pins. But, for me the quantifications are misleading until the qualifications are correct. . .

jorgekafkazar
January 28, 2011 12:38 pm

Hmm. One thing that might help the reader (it sure helps me) is to carry along the units in every equation, term by term. This lets me verify that all terms have consistent units. For instance:
Example I: Force = mass times acceleration
F [in Newtons (i.e., kg.m/sec²)] = m [in kil’ograms] * a [in meter/sec²]
Example II: Net Force = Applied Force – Friction
Net Force [in Newtons] = Applied Force [in Newtons ] – (Normal Force [in Newtons] * Coefficient of Friction [unitless])
I also recall seeing somewhere that the temperature exponent of 4.0 in the Stefan-Boltzmann Law was only valid for perfect black bodies. The Earth is not a perfect black body.

Tim Folkerts
January 28, 2011 12:45 pm

The mere fact that so many people are commenting about the units indicates that there is a problem — whether the problem is with nomenclature or the science is mostly a matter of semantics.
* traditionally, “E” and “Q” would be used for energy (e.g. J or ZJ)
* in this discussion, “E” and “Q” are generally used for power (energy/time; e.g. ZJ/year)
* in E = εσ(Ts)^4, “E” would be power/area (e.g. W/m^2). To make this work, either ε would have to include the surface area of the earth somehow, or the equation would have to change to εσA(Ts)^4.
My suggestion would be to more precise in usage and more precise is stating exactly what each quantity is being used for.
On a different front, I started to wonder about different energy contributions …
Human energy use from burning fuels is about 0.5 ZJ per year; we could call this “F”.
Geothermal energy flow up from below is about 1 ZJ per year; we could call this “G”
This would make the equation: E + dH/dt = Q + F + G. Of course, both of these are pretty small, but they would add to about 10% as much energy as is entering/leaving the oceans. Are there other significant sources/sinks of energy?

E.M.Smith
Editor
January 28, 2011 12:45 pm

Very well done. Very well done indead.
Yeah, I perked up on Ansatz as well. A reasonable translation would be “guess”…
We’re basing all this on a GUESS.
Also: Here it must be stressed that C is an effective heat capacity that reflects only that portion of the global heat capacity that is coupled to the perturbation on the time scale of the perturbation.
Caught my eye. This is another of the Great Leap Forward moments… 😉
They assume they have a clue what the heat capacity is. This is just so full of errors I don’t know where to start. It assumes there will be no long term change in the formation or destruction of ice, for example. It assumes there will be no long term change in the overturning of the oceans. (They even dance around saying that further down with the bit about heat stored in the surface layers; yet changes in the curcumpolar currents can change the rate of overturning of the world ocean and cause significant changes in surface temperatures and thus assumed or implied heating / cooling. Just look at ENSO variations). And so much more.
They (warmer “climate scientists”) have built a fantasy world on guesses, assumptions, and broken physics (averaging an intensive variable, temperature, from different objects / places) and think it has meaning. All it has is such confusion that it’s hard to show how broken it is. Like the person speaking complete bafflegab, it’s so broken you can’t begin to get a handle on straightening it out.
What you have done is found that handle to grab…
Oh, I’d also note in passing that they assume all heat must be radiated as IR from the TOP of the atomosphere. This implies that there is NO IR transmissive window at all from the surface. Yet surfaces will drop to very cold temperatures very quicking (with variance by object… that old fractal surface problem…) as they see an apparant very low IR night time sky temperature. Point an IR thermometer at the sky some cold dark night. Surprised at how “cold” it is? If that “top of the sky” is doing all the radiating, it’s gotten darned cold up there…
And what happens to all their assumptions if the CO2 is NOT CO2 at altitude?
This Just In: As of 11 Jan 2011 we’ve found out that CO2 and H2O can combine to form stable carbonic acid gas at temperatures as high as -30 C.
So what happens to all that CO2 “forcing” if the CO2 isn’t there? …
http://chiefio.wordpress.com/2011/01/27/fizzy-sky-ir-spectrum-is/
No, it’s not “settle science”, but that’s the whole point. We just don’t know what’s going on. So maybe those “way below -30 C” night sky IR temps are simply the result of the CO2 and water making a substance that does not block IR very well at night. Now that whole “top of the atmosphere” assumption exits and we get something rather like what we really see. My windshield frosts over from direct IR radiation even at air temperatures that do not support frost. Direct surface to space IR transport of heat?
I’m beginning to think more scientists need to be sent off to Cowboy Camp for a year or three to get them oriented to what a night sky feels like…

KR
January 28, 2011 1:04 pm

Willis Eschenbach 80
The upper 90 m of the ocean (the “well mixed” zone where wind driven circulation moves energy around relatively quickly) would alone add about a 6 year time factor for an instantaneous change in heating. Considering the deep layers with thermohaline circulation adds another 10-100 years (would be ~230 without circulation).
Hence my statement that yearly or worse yet quarterly air temperature correlations are worse than useless – you’re essentially looking at the correlation with noise. You really need decadal or multi-decadal trends to see what’s going on in climate, as opposed to weather. Inherent system variability (El Nino, for example) will slop energy around enough on shorter timescales that you simply cannot see the trends.
As to the second “substitution” objection: As I posted in 64, we know the surface temperatures (repeated, multiple direct measurements). We know the expected black-body radiation in IR based upon that temperature. And we have decades of satellite observations of the actual space-going IR to show us how much energy is actually emitted.
Put those three data together and you directly get the effective emissivity of the Earth to space.
E = ε σ Ts^4 is the Stefan-Boltzmann equation; the classic thermal radiation relationship. I suspect it was not numbered in the original because it’s accepted science, not a newly introduced equation to be justified. My reaction about “disproving” was in relation to your apparent issues with the Stefan-Boltzmann relationship.
We know the temperature of the surface, we know what is emitted to space, and via the S-B equation we get the effective emissivity. There’s simply no issue there.

Ron Cram
January 28, 2011 1:04 pm

Willis,
I was just reading a paper by Chylek and wondered what you would think of the equations in that paper. I’m not giving you homework. I’m just saying I would be interested in your analysis.
http://www.knmi.nl/~laagland/KIK/Documenten_2008/2007JD008740.pdf

Tim Folkerts
January 28, 2011 1:06 pm

Heat capacity, usually denoted with a capital “C”, has dimensions of [Energy/Temperature], for example J/K or BTU/˚F
Specific heat capacity, usually denoted with a lowercase “c”, has dimensions of [Energy/Temperature/mass], for example J/(kg*K) or BTU/(lb˚F)
I have never seen heat capacity include time, nor Q include time.
Roger Sowell says: January 28, 2011 at 11:34 am
Q is heat flow in Btu/hour (or similar heat per time units),
Cp is the heat capacity constant, expressed in Btu/hr/pound/degree F

Perhaps that is the convention in some areas of engineering, but again, that highlights the need to be very explicit in defining how the symbols are used, since different people my be interpreting the symbols differently

KR
January 28, 2011 1:07 pm

Willis – “You have the lovely habit of being specific about your objections and your thoughts.” – Thank you, I make an attempt to do so, and appreciate the feedback.

Brian H
January 28, 2011 1:40 pm

Charles Higley says:
January 28, 2011 at 5:59 am
I have a quick, maybe simple, question. The discussion mentions a connection between the upper level temperature (emissivity) and the surface temperatures. However, since heat which goes into evaporation is temperature neutral (not being observed as a temperature change in the lower atmosphere)

Say what? Evaporation causes powerful cooling of any surface, and nearby air. Else what’s perspiration for?