Explaining how the water vapor greenhouse effect works
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Increased CO2 makes more water vapor, a greenhouse gas which amplifies warming |
Climate Myth...
Water vapor is the most powerful greenhouse gas
“Water vapour is the most important greenhouse gas. This is part of the difficulty with the public and the media in understanding that 95% of greenhouse gases are water vapour. The public understand it, in that if you get a fall evening or spring evening and the sky is clear the heat will escape and the temperature will drop and you get frost. If there is a cloud cover, the heat is trapped by water vapour as a greenhouse gas and the temperature stays quite warm. If you go to In Salah in southern Algeria, they recorded at one point a daytime or noon high of 52 degrees Celsius – by midnight that night it was -3.6 degree Celsius. […] That was caused because there is no, or very little, water vapour in the atmosphere and it is a demonstration of water vapour as the most important greenhouse gas.” (Tim Ball)
At a glance
If you hang a load of wet washing on the line on a warm, sunny day and come back later, you can expect it to be dryer. What has happened? The water has changed its form from a liquid to a gas. It has left your jeans and T-shirts for the air surrounding them. The term for this gas is water vapour.
Water vapour is a common if minor part of the atmosphere. Unlike CO2 though, the amount varies an awful lot from one part of the globe to another and through time. Let's introduce two related terms here: 'non-condensable' and 'condensable'. They set out a critical difference between the two greenhouse gases, CO2 and water vapour.
Carbon dioxide boils at -78.5o C, thankfully an uncommon temperature on Earth. That means it's always present in the air as a gas. Water is in comparison multitalented: it can exist as vapour, liquid and solid. Condensed liquid water forms the tiny droplets that make up clouds at low and mid-levels. At height, where it is colder, the place of liquid droplets is taken by tiny ice-crystals. If either droplets or crystals clump together enough, then rain, snow or hail fall back to the surface. This process is constantly going on all around the planet all of the time. That's because, unlike CO2, water vapour is condensable.
CO2 is non-condensable and that means its concentration is remarkably similar throughout the atmosphere. It has a regular seasonal wobble thanks to photosynthetic plants - and it has an upward slope caused by our emissions, but it doesn't take part in weather as such.
Although water vapour is a greenhouse gas, its influence on temperature varies all the time, because it's always coming and going. That's why deserts get very hot by day thanks to the Sun's heat with a bit of help from the greenhouse effect but can go sub-zero at night. Deserts are dry places, so the water vapour contribution to the greenhouse effect is minimal. Because clear nights are common in dry desert areas, the ground can radiate heat freely to the atmosphere and cool quickly after dark.
On the other hand, the warming oceans are a colossal source of water vapour. You may have heard the term, 'atmospheric river' on the news. Moist air blows in off the ocean like a high altitude conveyor-belt, meets the land and rises over the hills. It's colder at height so the air cools as it rises.
Now for the important bit: for every degree Celsius increase in air temperature, that air can carry another 7% of water vapour. This arrangement works both ways so if air is cooled it sheds moisture as rain. Atmospheric rivers make the news when such moisture-conveyors remain in place for long enough to dump flooding rainfalls. The floods spread down river systems, causing variable havoc on their way back into the sea.
Atmospheric rivers are a good if damaging illustration of how quickly water is cycled in and out of our atmosphere. Carbon dioxide on the other hand just stays up there, inhibiting the flow of heat energy from Earth's surface to space. The more CO2, the stronger that effect.
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Further details
When those who deny human-caused global warming use this argument, they are trying to imply that an increase in CO2 isn't a major problem. If CO2 isn't as potent a greenhouse gas as water vapour, which there's already a lot of, adding a little more CO2 couldn't be that bad, they insist.
What this argument misses is the critical fact that water vapour in air creates what scientists call a 'positive feedback loop'. That means it amplifies temperature increases, making them significantly larger than they would be otherwise.
How does this work? The amount of water vapour in the atmosphere has a direct relation to the temperature in any given region and the availability of water for evaporation. Heard the weather-saying, "it's too cold to snow"? There's more than a grain of truth in that; very cold air has a low capacity for moisture.
But if you increase the temperature of the air, more water is able to evaporate, becoming vapour. There's a formula for this, the figure being 7% more moisture capacity for every degree Celsius of warming. All you then need is a source of water for evaporation and they are widespread - the oceans, for example.
So when something else causes a temperature increase, such as extra CO2 emissions from fossil fuel burning, more water can evaporate. Then, since water vapour is a greenhouse gas, this additional moisture causes the temperature to go up even further. That's the positive feedback loop.
How much does water vapour amplify warming? Studies show that water vapour feedback roughly doubles the amount of warming caused by CO2. So if there is a 1°C upward temperature change caused by CO2, the water vapour will cause the temperature to go up another 1°C. When other demonstrable feedback loops are included, and there are quite a few of them, the total warming from a 1°C change caused by CO2 is as much as 3°C.
The other factor to consider is that water evaporates from the land and sea and falls as rain, hail or snow all the time, with run-off or meltwater returning to the sea. Thus the amount of water vapour held in the atmosphere varies greatly in just hours and days. It's constantly cycling in and out through the prevailing weather in any given location. So even though water vapour is the dominant greenhouse gas in terms of quantity, it has what we call a short 'atmospheric residence time' due to that constant cycling in and out.
On the other hand, CO2 doesn't take an active part in the weather. It does hitch a lift on it by being slowly removed from the air as weak solutions of carbonic acid in rainwater. These solutions are key weathering agents, affecting rocks on geological time-scales. Weathering is a key part of the slow carbon cycle, with the emphasis on slow: CO2 thus stays in our atmosphere for years and even centuries. It has a long atmospheric residence time. Even a small additional amount of CO2 thus has a greater long-term effect - and in our case that additional amount is far from small.
To summarize: what deniers are ignoring when they say that water vapour is the dominant greenhouse gas, is that the water vapour feedback loop actually amplifies temperature changes caused by CO2.
When skeptics use this argument, they are trying to imply that an increase in CO2 isn't a major problem. If CO2 isn't as powerful as water vapor, which there's already a lot of, adding a little more CO2 couldn't be that bad, right? What this argument misses is the fact that water vapor creates what scientists call a 'positive feedback loop' in the atmosphere — making any temperature changes larger than they would be otherwise.
How does this work? The amount of water vapor in the atmosphere exists in direct relation to the temperature. If you increase the temperature, more water evaporates and becomes vapor, and vice versa. So when something else causes a temperature increase (such as extra CO2 from fossil fuels), more water evaporates. Then, since water vapor is a greenhouse gas, this additional water vapor causes the temperature to go up even further—a positive feedback.
How much does water vapor amplify CO2 warming? Studies show that water vapor feedback roughly doubles the amount of warming caused by CO2. So if there is a 1°C change caused by CO2, the water vapor will cause the temperature to go up another 1°C. When other feedback loops are included, the total warming from a potential 1°C change caused by CO2 is, in reality, as much as 3°C.
The other factor to consider is that water is evaporated from the land and sea and falls as rain or snow all the time. Thus the amount held in the atmosphere as water vapour varies greatly in just hours and days as result of the prevailing weather in any location. So even though water vapour is the greatest greenhouse gas, it is relatively short-lived. On the other hand, CO2 is removed from the air by natural geological-scale processes and these take a long time to work. Consequently CO2 stays in our atmosphere for years and even centuries. A small additional amount has a much more long-term effect.
So skeptics are right in saying that water vapor is the dominant greenhouse gas. What they don't mention is that the water vapor feedback loop actually makes temperature changes caused by CO2 even bigger.
Last updated on 23 July 2023 by John Mason. View Archives
Tom Curtis #138, I wanted to add (correct it if wrong) that the forcing value is a theoretical value. It's as if the entire change were done instantly. In reality, we experience CO2 increases, not from 1x (of some arbitrary value) to 2x overnight, but as small increments over time, so the imbalance is likely never to get very large at all. The 1x is a reference point and the 3.7 forcing value is a theoretical imbalance that would exist if the 2x happened right away ("with surface and tropospheric temperatures and state held fixed at the unperturbed values").
Jose_X @139, that is mostly correct.
As noted @138 (point 2) , the CO2 forcing is the total net change in TOA upward IR flux before (or excluding) temperature adjustments. Clearly if we add the CO2 incrementally, there will be temperature adjustments so that the TOA energy imbalance will be significantly less than the CO2 forcing. But, the forcing is the same at 2xCO2 regardless of whether it is added incrementally or as a single slug.
That does not differ from your explanation except in terms of what is meant by "theoretical variable". Roughly (as it is a while since I studied this), a theoretical variable in physics is a value which is an element of an empirical theory that is not directly measurable itself, but whose values have direct implications for measurable variables. In this sense, forcing is "theoretical". You appear to treat "theoretical" as a synonym for "hypothetical" which would be incorrect.
Tom Curtis, thanks for the response, but I was thinking of "theoretical" just as you explained, meaning that if we could actually do 2x over night then we would observe the full forcing value.
Jose_X @141, fair enough. In that case, however, you should have written "the 3.7 forcing value is a theoretical imbalance that would exist only be directly measurable if the 2x happened right away" or possibly, "the TOA energy imbalance would only equal the forcing if the CO2 was doubled instantaneously".
Even that is not perfectly accurate, in that short term fluctuations in temperature result in short term departures from radiative equilibrium, but they are small relative to the 3.7 W/m^2 forcing from doubling CO2.
Tom Curtis, thanks for the response, but I was thinking of "theoretical" just as you explained, meaning that if we could actually do 2x over night then we would observe the full forcing value.
Tom Curtis #142. Rethinking the meaning of the words now after your 142 comment, I see that you were right and I did mean hypothetical. I didn't mean that the value couldn't exist under any circumstance, but rather that it could but would not unless the CO2 were eg done "over night". I concluded this from the statement by the IPCC (quoted on Wikipedia) that a reference value is used to define the forcing ("with surface and tropospheric temperatures and state held fixed at the unperturbed values") so that perhaps a perturbation "forcing" is not an entity (theoretical or measurable) that is manifested in reality if there isn't an imbalance at TOA of that magnitude at any given point in time.
Let me ask something about the meaning of the word "forcing". Would "yes" be the answer to the question, "is the forcing at TOA from CO2 a value greater than 5 W/m^2?" [ie, is it clearly greater than the 2x forcing quoted by the IPCC because it would include contributions from all CO2 in the atmosphere today?]
Jose_X - It's a bit difficult to understand what you are discussing here. Are you asking for the current sum value of CO2 forcing? According to NASA numbers CO2 represents ~20% of the current greenhouse effect, water vapor and clouds ~75%, and other gases (methane, CFCs, ozone, etc) another 5%.
33C of greenhouse effect, or 6.6C directly attributable to CO2 by those numbers, means about 22-23 or so W/m^2 of total CO2 forcing at this time.
On the other hand, "forcing" is generally referred to as the change from previous conditions, usually 1750AD, in which case as of 2005 CO2 accounts for ~1.66 (1.49-1.83) W/m2 as a delta. Add in all the other factors +/-, and the total net anthropogenic forcing change since 1750 is about 1.6 (0.6-2.4) W/m2.
[Source]
But again, I'm not entirely certain what you are asking about.
I was not looking at "forcing" as something like a gravitational force value associated with a body on the earth (which tends to exist all the time) but more like (net) heat, a quantity defined as the summation of other (sign-dependent) quantities and which might frequently approach or be zero. I guess that was wrong.
So, to confuse everyone still further, I guess forcing is somewhat analogous to pressure in that it tends to be nonzero and significant whether the system is approximately in equilibrium or not and under a context where "pressure" would refer to partial pressure of a species or, more specifically, to the additional contribution to partial pressure that would be provided as the species moves from one reference concentration to a different target point separated from the first by a stadardized multiple (of 2).
Are the following observations correct?
And does someone have an answer for the two questions at point 3.
1. The forcing value depends on the reference sun intensity. If the sun was providing approximately a stable 50 W/m^2 TOA, then the CO2 forcing calculations would yield different numbers.
2. For the lambda (climate sensitivity proportionality coefficient) between forcing at TOA and (yearly global mean) temperature on the surface to be approximately constant, we should use a reference point for forcing such that the delta temperatures involved are at most a few K. [This criteria would include a "near" constant solar intensity requirement that has easily been met by sun+albedo across spans of a few centuries.] This would allow, for example, the relevant Stefan Boltzmann relationships to remain in an approximately linear region, eg, where each degree change in temp would correspond approximately to a constant change in W/m^2 (currently approaching 5.4 W/m^2 per C at ground level).
Also, I was guessing that, although the lambda and forcing values might be determined from computer programs that may potentially take a long time to run in order to achieve a high level of accuracy, that using simple models (esp linear) afterward with those derived values allows researchers to ask and answer many questions involving lots of combinations of forcing agents and quantities without having to run involved simulations for every such combination of values. The simple models also help us understand the main factors in climate change and together with all models used help keep a sanity check on each other.
3. Calculating the contributions from CO2 to the greenhouse effect (using data from KR's recent comment):
287.5 - 255.5 = 33 (relevant temperature values to nearest 0.5 C)
33 / 6.6 = 5 (aka, 20% contribution by CO2)
387.38 - 241.63 = 145.75 (Stefan Boltzmann W/m^2 at surface corresponding to 33 C increase and e=1)
145.75 / 5 = 29.15 (contribution by CO2 to total W/m^2 at surface)
So there have been 29.15 W/m^2 of warming due to CO2 for its 6.6 C contribution to the total greenhouse effect of 33 C.
Question 1: How do we calculate the total forcing by CO2 that led to this 29 W/mSq?
Put differently, if we revert to an atmosphere with almost no ghg effect, meaning that the TOA and surface are roughly at 255K, how many times will we have to apply a forcing of 1 W/m^2 (TOA) from CO2 additions to get to our current atmosphere? Can someone roughly (including hand waving) show the steps in unit increments that achieve this and so that we can see how the ground temp or ground irradiance change at each step? [For the purposes of addressing this question, on may optionally assume H2O is liquid all throughout the 33 C range.]
Question 2: Whatever approximation method is used to answer Question 1, will we get roughly the same answer if we go in 5 W/m^2 increments?
My confusion is that forcings are defined at TOA yet TOA always reverts to about 240 W/m^2. And there isn't to me an obvious way to derive that total forcing value (eg, from CO2.. or even from all ghg) simply from knowing how much change was experienced on the ground (the greenhouse effect). I can see how that question might be answered possibly by calculating in delta/differential steps and taking a limit in order to try and get a unique result (although I don't know how to make that calculation). Alternatively, it might not be possible to get sequence/limit convergence to a unique value on a "delta" analysis. I don't know, and before I spend more time thinking about this problem, I'm curious if someone has access to an online reference where I can get the answer or if they can provide the answer themselves.
Resolving these questions makes it easier for me to address more definitively some skeptical questions I have been getting related to "forcings" math (and in understanding this for its own sake).
Jose_X - Some misconceptions here, if I might point them out (hopefully correctly).
"How do we calculate the total forcing by CO2 that led to this 29 W/m^2?"
If you start from zero CO2, the forcing per increase in CO2 concentration starts linear, and becomes logarithmic as various bands reach saturation (with increases coming from band widening, rather than peak increases), so the relationship is not consistent over concentrations. Methane (IIRC) is still in the linear region, CO2 is not. The accurate answer comes from line-by-line radiative codes such as MODTRAN using the HITRAN spectral database - essentially numeric integration. You have to do the math. There is no simple equation.
"My confusion is that forcings are defined at TOA yet TOA always reverts to about 240 W/m^2"
Yes, it does, as 240 W/m^2 is what is incoming from the sun. When enough time elapses for GHG forcing changes to come to equilibrium, energy out = energy in at TOA, although at a different surface temperature depending on those changes. The only reason for that equilibrium number to change would be changes in incoming energy, perhaps from albedo/land use or significant cloud percentage/distribution. I do expect that the melt of the Arctic ice cap, for example, will raise that equilibrium number somewhat by decreasing summer albedo.
Jose_X @146:
1) Because the CO2 modulates the outgoing LW radiation, it depends on the strength of that radiation, and hence on surface temperature. That does mean it depends on the strength of the incoming solar radiation, but only indirectly. In contrast, changes in aerosol opitical depth, which change albedo, are directly dependent on the strength of the incoming solar radiation for the strength of the forcing.
2) Across the range of temperatures and conditions experienced in the Phanerozoic (approx -6 to +8 C relative to present values) λ has been fairly constant, with changes in continental configurations having a much larger effect on changes in λ than variation withing the temperature range. In broader terms, λ becomes significantly larger as ice sheets approach 30o Latitude (North or South) due to the much enhanced albedo, and as temperatures rise significantly beyond 8 C above current values (due to enhanced water vapour feedback).
Other than noting that your second equation in section (3) should be 33/5 = 6.6, I will return to it when I have a bit more time.
Tom Curtis, actually the equation should probably have been 6.6/33 = .2 (aka, 1/5) and then rather than divide the 5 into the 145.75 I would have multiplied the .2 and 145.75. Point is that 6.6 is 20% of the whole change as expressed in C so I wanted to find that same 20% of the whole change in W/msq.
KR, calculating the forcing for CO2 early on in the process (near 0% CO2) and continuing, eg, using at each step the integration process you mentioned, is what I imagined might be done. But I am curious if that procedure would lead to the same total forcing result no matter in how many steps we calculate the increments.
As an extreme example, if we calculate the forcing of one additional molecule of CO2 at a time (assuming the standard model we use now applies, eg, ignoring quantum or other effects that might be present at very low concentrations or what not, and assuming that computation could finish some day), what total forcing would we get and would this value be the same if after an initial start we switch over to steps where we double the prior value.
Why do I care? I would like to know if the forcing calculations adhere to linear superposition like linear operators do with vector (tensor?) quantities (ie, partitioning into component parts arbitrarily, operate on these separately, and then combined back additively into a unique whole). The definition of forcing makes me a little nervous about that.
Does someone have software that can simulate several reasonable partitions for the current CO2 to test if each partitioning path leads to the same answer? [An example might be to calculate 1 W/msq of forcing at each step vs 2 W/msq at each step. In fact, there is no need to do this until the current atmosphere. We can just compare 1 W/sqm for 40 steps vs 2 W/sqm for 20 steps.]
[In these replies I giving, m^2 is same as mSq is same as sqm ...etc. I get lazy with the keystrokes sometimes.]