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:
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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What part does heat emanating from the Earth’s Core play in all this?
ntesdorf
“The Cold Equations” was a story in Analog Science Fiction magazine. I can’t remember the author, but if I had the time to examine my complete collection of ‘Astounding/Analog Science Fiction’ which has never been indexed I’m sure I could find it. I remember both the title and the story from about 50 or so years ago.
Willis,
I disagree a little with you here … “It is useless to simply say “dH/dt = Cp dT/dt is absolutely valid” without a single theory, fact, or observation to back up your claim. ”
Pretty much the definition of heat capacity (at constant pressure) is [heat that flowed into an object]/[change in temperature]. Traditionally this is written as
Cp = Q/ΔT
but with the nomenclature used here this becomes
Cp = – dH/d(Ts) [dH is the energy LEAVING, not entering the ocean].
Rearranging and finding the energy per year gives
– dH/dt = Cp d(Ts)/dt
Other than the minus sign, the biggest problem to me is that they use d(Ts) (the surface temperature change) as a proxy for the change in temperature of the some nebulous amount of upper ocean. Clearly the two ought to be related (if the top meter is warming, then some warming throughout the relevant layers should also be occurring, although the correlation may not be great.)
In Burrito said “That’s because a 1 degree increase at the poles will yields a relatively greater change in long wavelength radiation that a 1 degree increase at the equator, ”
Isn’t the opposite true? Since energy is a function of T**4? and temps are higher near the equator?
The Cold Equations available as an ebook where there’s an explanation and history in the preface. The actual short story is not among the available ‘sample chapters.’
For Malcolm Miller
The Cold Equations – Wikipedia, the free encyclopedia
“The Cold Equations” is a science fiction short story by Tom Godwin, first published in Astounding Magazine in 1954. In 1970, the Science Fiction Writers of …
Summary – Reactions – Allegations of borrowing – Adaptations
en.wikipedia.org/wiki/The_Cold_Equations – Cached – Similar
“”””” 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 49 times in three short years. 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. “””””
And here’s where I would disagrre with you Willis:- “”””” and longwave (thermal infrared) radiation emitted at the top of the atmosphere E. “””””
I suggest that only a small portion of the LWIR emission to space, actually comes from the top of the atmosphere; where the molecular and atomic density is evanescent, and hardly capable of emitting anything like 390 W/m^2 upwards.
A good bit of the outgoing LWIR originates from the very surface of the earth, corresponding to the various ranges of surface Temperature that can be found on earth all at the same time.
The heat capacity at the top of the atmosphere has to be so low, that any emission at all, would cause the temperature to plummet, if it wasn’t being constantly replenished from below.
Do we actually have something like a measured complete spectroscopic plot of the outgoing radiation from earth say from 0.1 to 100 microns, at a resolution capable of showing all the important components ? I have some “simulated” ones for a much smaller part of the external view, that clearly don’t have all the expected components present and accounted for.
Malcolm Miller says:
January 28, 2011 at 2:08 pm
> “The Cold Equations” was a story in Analog Science Fiction magazine. I can’t remember the author,
Willis provides a link to http://en.wikipedia.org/wiki/The_Cold_Equations . Has more information than I thought existed.
Great post, Willis. The Cold Equations was written by Tom Godwin, and published by Analog,
It seems to me that these equations for C and epsilon are definitions in terms of long-term trends. If ocean heat content increases, so will Ts, and C is the proportionality constant. If surface temperature increases, so will outgoing radiation and epsilon is the proportionality constant. It is very clear to me that these were not intended to describe time-scales as short as inter-annual variability, but more the climate time-scales. Their Ansatz is therefore to define these proportionality constants for a simplified model of climate-scale variations.
If the assertions in this post are true, these seem like pretty egregious thermodynamics errors. Why not publish these results in a real journal instead of a blog? Be sure to post again if the paper is approved. Maybe this would overturn parts of AGW.
I hope the articles below aren’t true, otherwise credentials would be questionable:
[snip]
[You can link to opinions that Willis Eschenbach is “lying” on many different blogs. But not here. ~dbs, mod.]
Willis, thanks for the math showing the fallacy of regarding the earth’s radiative balance as a relatively simple function of its average surface temperature (whatever that is; note that Dr. Hansen’s GISStimate of the “average” temp for a given year — e.g. 1940 — changes as time passes; who knew Ts varies both with and without time?).
With regard to the story, like others here I was impressed by it when I read it as a kid. The Wiki article references an interesting critique of the story’s premise here:
http://www.writing.com/main/view_item/item_id/1204039-BS-Flag-on-The-Cold-Equations
I also recall reading a probably derivative novel “High Vacuum” in which a lovestruck female stows away on the first moon mission, causing it to crash for lack of fuel:
http://en.wikipedia.org/wiki/High_Vacuum
To this day I suspect the problems on Apollo 13 were really caused by a stowaway. 🙂
One of my first posts on CA years ago was the impossibility of inferring too much from T measurements that were half daily max + min. This early act assumes a distribution that is artificial and it affects all downstream discussions about distributions. Specifically I objected to this measure being used as a stand-in for H.
This rather limits the discussion on distributions to the period where daily T is measured many times a day, say from 1990 onwards or even later.
Willis, your post questions the T to H equivalence and rattles the cage of orthodoxy again. These early “balance” authors were trying to get away with plots as bad as a movie script – like “The Heat of the Night” which was popular for black body radiation of a magic property named charisma (units unknown).
Willis points out:
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
Summary of Substitution 2: E = ε σ Ts^4
This substitution is, quite demonstrably, either mathematically wrong or meaninglessly true as an identity.
—
Willis, this seems half-science, I don’t agree with the top and the bottom question depends on the limits and exact definition. I have commented hear long enough that you know I usually have a hard time placing in words what is in my thoughts, but I’ll try here on one isolated aspect and this is not strictly addressed toward you for I’m sure you already know everything I am about to say, maybe.
What does Ts, the temperature at the surface, tell us at the surface? Well, it is a temperature so it merely tells us at that very point what the kinetic energy is by the mean velocity of the molecules. But says absolutely nothing of where that energy goes during the next dt (increment of time), does it?
I can immediately see at least four aspects that occur and let’s start with only the oceans being 71% of the surface. Some will always go into the water below dictated by specific heat and conductivity and the temperature below. Some will go into (or be added coming out) via latent heat for there is always evaporation/condensation occurring at the ocean interface. This is largely dictated by the wind velocity and turbulence to remove the saturated air from the surface but it is always there. Some of that energy will go into the creation of winds itself, and ocean currents though tiny.
After subtracting all of these energy fluxes (uses) from Ts then you can compute (maybe only by numeric integration for I can’t imagine a closed form set of equation here) what energy is left that can then be transferred by radiation, but, the Ts value is no longer the same as before, that is, the Ts that can radiate by that equation above. If you just use the equation above then ALL of the energy from Ts is going to radiation, nowhere else, and that clearly, and logically, is not the case. The same happens at the soil interface but with different parameter values.
We all know in the tropics it is evaporation rules. All of the energy, some 2350 J/cm3 of evaporated water, must be subtracted from the energy at the surface before radiative equations can come into play. It’s a figment. They are way overstating the radiation in these cases.
Yes, as they did, you can smear this over such a long period of time that most, if not all, of these effects cancel but you have then smeared out all of the resolution to be able to say if anything is actually different for one month or year to the next. Sounds a little like the uncertainty principle doesn’t it? That curious, though not really the same.
One more big point. If energy is spread evenly over a surface, the radiation emitted at T will ALWAYS be less that if the exactly same quantity of energy is lumped in certain areas with other areas cooler. That is what the fourth power causes instantly and that is why you really can’t average the energy evenly over the Earth in the first place and hope to get true science out. Even though radiation rules all aspects as viewed far away as from space, input equals output, it is the non-radiative energy fluxes that rule the movement of energy upward so radiation to space can easily occur (yes, I know of the window and optical thickness, altitude dependence).
IPCC and certain climatologists seem to toss all of that reality out of the window and into the wind and this warped view is carried along (sometimes by many here) without realizing all of the subtle mistakes that just occurred in their statements, intentional or not. When real physics get into this arena, I hope soon, we will finally start to get some correct answers.
I’ll stop rambling. I have one more comment but will stop here at a good breakpoint.
KR says:
January 28, 2011 at 9:40 am
KR, you are kinda correct in that. Yes, you can take an average of TOA upwelling / surface upwelling.

The problem is, as you can see here, the correlation between surface upwelling and TOA upwelling (as modeled by the GISS climate model), is very, very poor (r^2 = 0.00). This agrees with the ERBE figures available here, which again show abysmal correlation with σ Ts^4 (using GISSTEMP global temperatures). Here’s that comparison.
Figure W1. Top-of-atmosphere (TOA) upwelling radiation and surface upwelling radiation. Surface upwelling radiation is calculated using the GISSTEMP global temperature anomaly with an assumed global average temperature of 288 Kelvin. Note the total lack of correlation between the surface and the TOA emissions.
So while multiplying the surface upwelling radiation by 0.62 (the approximate value of their epsilon ε) gets their answer into approximately the right range, from there you’d do better using a straight line.
Finally, the ERBE records cover 15 years. Over that period, in line with the surface warming, the surface upwelling radiation increased at 1.12 W/m2 per decade. Over the 15 years, the total increase in surface upwelling was 1.7 W/m2. On the other hand, TOA longwave emissions stayed almost dead flat … which again argues against the idea that you can use a linear transform of surface radiation as a proxy for TOA radiation. Over the period of the ERBE record, using any such transform would have given a very wrong answer.
w.
The problem with that is it assumes all the heat radiated transits all the CO2. It doesn’t. If you have vapor condensing into ice at very high altitude, a large amount of heat is lost well above the CO2. Same thing even with water vapor condensing at anything >20,000 feet. It is well above most of the CO2. If all the heat were radiated from the surface, the argument would have some validity but a large amount of heat is moved via evaporation and condensation that transits a large portion of the CO2 before it is released as longwave IR.
For example, a large amount of the heat generated by the human body is transported thousands of feet aloft by the wind and then released when our sweat condenses at high altitude.
If you can quantify how much heat is released at which altitude, you can then begin to get a realistic grip on the impact of atmospheric CO2. Absorption of heat by CO2 isn’t really a matter of the relative quantity of the total atmosphere (ppm of the atmosphere made up of CO2), it is a function of the absolute density of CO2 between where the heat is released and the top of the atmosphere.
If you release longwave IR in an area where there are few molecules of CO2 to absorb it, it doesn’t matter what the percentage of CO2. Some small percentage of almost nothing is less than almost nothing.
A number of people have said that temperature is not a flow. However, temperature can be converted to the equivalent blackbody radiation flow using the familiar Stefan-Boltzmann formula.
Think about it this way. My body is at about 37°C. Like anything at that temperature, there is a constant flow of radiative energy emanating from my body, 525 W/m2. How, then, is a temperature of 37°C not equivalent to a flow of 525 W/m2?
w.
FrankK says:
January 28, 2011 at 10:57 am
Hi, Frank. No, that’s not what I’m saying.
In a situation where temperature differential is driving the temperature change, or equivalently where hydraulic head is driving the volume change, that relationship holds. But in this situation, atmospheric temperature is not driving ocean heat content changes, it simply doesn’t have enough thermal mass.
w.
dwb says:
January 28, 2011 at 11:12 am
The crust is far too slow in picking up/releasing heat to function as an effective reservoir.
Interesting thought.
I agree:
The T,E and Q are flows statement is off.
The fridge analogy needs a little work.
If you define the units earlier you should see that the dH/dt = C dT/dt equation is right.
The plots of OHC and temperature change are interesting. Rapid change in OHC of the magnitude you show goes against what I would expect. It would be interesting to see what areas had the greatest short term changes in OHC.
In Burrito’s comment about how OLR changes from the poles to the tropics brings up a good point about emissivity and the uncertainty in determining Sensitivity. Dry air 2XCO2 Sensitivity is approximately 1 to 1.6 C. So at the poles, CO2 would be the dominate GHS. But the estimated ~3.3 C sensitivity (Gavin) is moist air. So I expect that the average emissivity is over estimated. How much I don’t know.
Willis: “My body is at about 37°C. Like anything at that temperature, there is a constant flow of radiative energy emanating from my body, 525 W/m2. How, then, is a temperature of 37°C not equivalent to a flow of 525 W/m2?”
Because the flow is not a linear function of temperature. In fact in your example, if your temperature increases much more, you will start sweating, and total energy flow will continue to increase while temperature will not (unless you are dehydrated).
Willis,
I do not think Schwartz believes that the ocean is warmed by the air. I believe he understands that it is mostly the other way around. After all, the majority of total solar energy reaching the earth’s surface is absorbed by the ocean surface layer. Most of that energy finds it’s way to space through the atmosphere.
I guess my problem with this is it implicitly assumes all physics and no chemistry or biology. That might be a mistake. How do the numbers add up?
In the oceans, algae absorb light and perform chemical reactions that convert light energy to biomolecules that require X kcal/mole to synthesize. Not all of that stored energy is returned to space. Some of it sinks to the bottom of the ocean. What percentage of the incoming radiation is captured and doesn’t get converted to heat?
On land, soil is formed through a decay process involving vegetable matter accumulated on land and grasslands. Coal is an example of stored solar energy from millions of years ago.
Changes in the amount of energy stored through chemical synthesis might be comparable to the effects of other factors in the energy balance. After all, we do have a lot of photosynthetic organsims on the planet, and quite a bit of biomass. It doesn’t all burn or decay back to CO2, H2O, NO3-, HSO4-, H2PO4- and so on. Living things are composed of cells, and the bulk of these cells need to divide regularly. Therefore, they need to take up nutrients. The majority of the biosphere depends on photosynthesis ultimately. But how many kg of biomass are left behind each year?
A very rough estimate of Net Primary Production is 100 Gt/yr of C (http://en.wikipedia.org/wiki/Biomass_(ecology)). If we take ‘C’ as referring to the typical photosynthetic reaction:
H2O + CO2 + light -> CH2O + O2, (http://www.solarnavigator.net/photosynthesis.htm)
each ‘C’ corresponds to 112 kcal/mole of stored energy. Working out the math, I get about 9 ZJ/yr of stored solar energy. Some of it goes back into the system as heat during decay.
Perhaps 9 ZJ out of 5500 ZJ is small, but I am not yet convinced it is negligible. How much of that 5500 just reflects off of clouds or the ocean surface? And biological effects can have other impacts. Transpiration certainly is a significant contributor to humidity, and thus cloud formation.
Obviously, the real world is not so simple as the energy equation we are talking about in the main post. But certainly I enjoyed the discussion!
Steve Reynolds says:
January 28, 2011 at 6:20 pm
Willis: “My body is at about 37°C. Like anything at that temperature, there is a constant flow of radiative energy emanating from my body, 525 W/m2. How, then, is a temperature of 37°C not equivalent to a flow of 525 W/m2?”
Because the flow is not a linear function of temperature. In fact in your example, if your temperature increases much more, you will start sweating, and total energy flow will continue to increase while temperature will not (unless you are dehydrated).
Energy flow is not linear function of temperature, but it is a KNOWN function of temperature, at least for radiative heat transfer, which is the only one that is being discussed here. Evaporative cooling, convection and conduction are not being used in radiative balance equations.
@ur momisugly Tim Folkerts at January 28, 2011 at 1:06 pm
Tim, my mistake, and you are correct, that the Cp should not have included units of time. It should be Btu/hr/degree F. The time unit should properly be with the mass, in pounds per hour. Thus, we have Q in Btu/hr = mass in pounds/hr x Cp in Btu/lb/degree F x (T2 – T1) in degrees F.
The continuous process industries use Q as Btu/hr and mass in pounds/hr. These industries include things such as chemical plants, petrochemical plants, natural gas processing plants, oil refineries, and many others. Every industrial plant with a fired heater or fired furnace uses these calculations.
The point remains that every element of each equation must be labeled and its units provided.