May 2013 CO2 Concentrations: 399.89 ppm

During May 2013, the Scripps Institution of Oceanography measured an average of 399.89 ppm CO2 concentration at their Mauna Loa, Hawai’i Observatory.

This value is important.  Why?  Because not only is 399.89 ppm the largest CO2 concentration value for any May in recorded history, it is the largest CO2 concentration value in any calendar month in recorded history.  More on that below.  This year’s May  value is 3.02 ppm higher than May 2012′s!  Month-to-month differences typically range between 1 and 2 ppm.  This jump is clearly well outside of that range.  This is more in line with February’s year-over-year change of 3.37 ppm.  The unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below, is more significant.

Let’s get back to that all-time high concentration value.  The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported last year and, prior to the last four months, in recorded history (neglecting proxy data).  I expected May of this year to produce another all-time record value and it clearly did that.  May 2013′s value will hold onto first place until February 2014.  I wrote the following three months ago:

If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400 ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – this means CO2 concentrations are another climate variable that is increasing faster than experts predicted just a short couple of years ago.

For the past few months, I stood by that prediction.  But actual concentration increases proved me slightly wrong.  Here is why: the difference in CO2 concentration values between May 2012 and March 2012 was 2.33 ppm (396.78 – 394.45).  If we do the simplest thing and add that same difference to March 2013’s value, we get 399.67 ppm.  That is awfully close to 400 ppm, but less than the 399.93 ppm extrapolation I first performed in February, which ended up being a perfect projection.  It’s also close to the 399.3 ppm extrapolation I calculated in March.  I discussed May 2013′s projection with Sourabh after February’s post.  They predicted 399.5-400 ppm concentration for May 2013.  I predicted NOAA would measure May 2013′s mean concentration near 399.3 ppm, but it turns out Sourabh was closer than I was to the actual value.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in May from 1958 through 2013.

CO2Now.org added the `350s` and `400s` to the past two month’s graphics.  I suppose they’re meant to imply concentrations shattered 350 ppm back in the 1980s and are pushing up against 400 ppm now in the 2010s.

How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values (red) from 2009 through 2013 (NOAA).  Monthly CO2 concentration values with seasonal cycle removed (black).  Note the yearly minimum observation occurred seven months ago the yearly maximum value occurred last month.  CO2 concentrations will decrease throughout the rest of 2013, as they do every year after May.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle based on monthly average values.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the recent and ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing of the Earth, which increases the amount of energy in our climate system.

CO2 concentrations are increasing at an increasing rate – not a good trend with respect to minimizing future warming.  Natural systems are not equipped to remove CO2 emissions quickly from the atmosphere.  Indeed, natural systems will take tens of thousands of years to remove the CO2 we emitted in the course of a couple short centuries.  Human systems do not yet exist that remove CO2 from any medium (air or water).  They are not likely to exist for some time.  So NOAA will extend the right side of the above graphs for years and decades to come.

This month, I want to spend some time on this post’s focus: CO2 concentration values.  Given our species penchant for round numbers, it came as little surprise that the corporate media placed an uncommon amount of attention on a value that has relatively low meaning: daily CO2 concentrations at Mauna Loa surpassed 400 ppm for a day during the month of May.  In fact, both the media and many climate activists made a very big deal about this development.  I think that was largely a waste of time.  Again, the daily value itself didn’t represent any large difference once reached.  The climate system did not automatically kick into a different setting once concentrations passed 400 ppm for a day.  Nothing substantially new occurred that didn’t when concentration were “only” 399 ppm (or 390 ppm or 380 ppm for that matter).

As I state in this series every month, the trend makes much more of a difference than any daily, monthly, or even yearly average value.  And that trend is accelerating upwards at a rate that many didn’t think was possible even 10 years ago.  The effects from last year’s average CO2 concentrations won’t manifest in realizable terms until 30-50 years from now.  I didn’t see anybody pointing out that important detail.  Similarly, I didn’t see any explanation that today’s mean temperatures are largely a result of CO2 concentrations from 30+ years ago.  Perhaps most importantly, climate activists didn’t mention that CO2 concentrations are rising at a rising rate despite decades of their activism.  That fact creates a rather uncomfortable situation because most activists are proponents of doing tomorrow what they did yesterday.  If those actions haven’t had any effect up until now, why the advocacy for the status quo when those same activists try to claim that the status quo is untenable.  If they really believed in their catastrophic climate change claims, shouldn’t they honestly evaluate the effects their actions have had?  And if those actions produced far less meaningful progress than they state is absolutely required for the survival of our species and the planet (grandiose language, I know), why do their strategies and tactics remain largely unchanged?

I write these posts for people who are curious or interested in the state of a key climate variable.  I realized that doomsday language turns a significant portion of my potential audience off from the get-go.  If we are to do something meaningful about climate change, we cannot afford the disengagement and hostility of one-third or more of our fellow global citizens towards climate activism.  I don’t want to simply treat people as empty vessels into which I can pour knowledge.  I want to engage them on ground that is similar between us precisely because I want to do something.  Screaming about 400 ppm mean CO2 concentration for one day and then walking away from the variable until we pass the next perceived meaningful threshold doesn’t strike me as engagement.

The rise in CO2 concentrations will slow down, stop, and reverse when we decide it will.  It depends primarily on the rate at which we emit CO2 into the atmosphere.  We can choose 400 ppm or 450 ppm or almost any other target (350 ppm seems out of reach within the next couple hundred years).  That choice is dependent on the type of policies we decide to implement.  It is our current policy to burn fossil fuels because we think doing so is cheap, although current practices are massively inefficient and done without proper market signals.  We will widely deploy clean sources of energy when they are cheap, the timing of which we control.  We will remove CO2 from the atmosphere if we have cheap and effective technologies and mechanisms to do so, which we also control to some degree.  These future trends depend on today’s innovation and investment in research, development, and deployment.  Today’s carbon markets are not the correct mechanism, as they are aptly demonstrating.  The bottom line is: We will limit future warming and climate effects when we choose to do so.

April 2013 CO2 Concentrations: 398.35 ppm

During April 2013, the Scripps Institution of Oceanography measured an average of 398.35ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory.

This value is a big deal.  Why?  Because not only is 398.35 ppm the largest CO2 concentration value for any April in recorded history, it is the largest CO2 concentration value in any month in recorded history.  More on that below.  This year’s April value is 1.90 ppm higher than April 2012′s!  Month-to-month differences typically range between 1 and 2 ppm.  This jump of 1.90 ppm is within that range.  It is also ~0.9 ppm less than March’s and 1.47 ppm less than February’s year-over-year change of 3.37 ppm.  The unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below, is more significant.

Let’s get back to that all-time high concentration value.  The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported last year and, prior to the last three months, in recorded history (neglecting proxy data).  I expect May of this year to produce another all-time record value.  That value will hold first place until February 2014.  I wrote the following three months ago:

If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – this means CO2 concentrations are another climate variable that is increasing faster than experts predicted just a short couple of years ago.

For the most part, I stand by that prediction.  But actual concentration increases might prove  me wrong.  Here is why: the difference in CO2 concentration values between May 2012 and March 2012 was 2.33 ppm (396.78 – 394.45).  If we do the simplest thing and add that same difference to this March’s value, we get 399.67 ppm.  That is awfully close to 400 ppm, but less than the 399.93 ppm extrapolation I performed in February.  It’s also close to the 399.3 ppm extrapolation I calculated in March.  I discussed May 2013′s projection with Sourabh after February’s post.  They predicted 399.5-400 ppm concentration for May 2013.  For the second month in a row, I think NOAA will measure May 2013′s mean concentration near 399.3 ppm.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in April from 1958 through 2013.

CO2Now.org added the `350s` and `400s` to this month’s graphic.  I suppose they’re meant to imply concentrations shattered 350 ppm back in the 1980s and are pushing up against 400 ppm now in the 2010s.

How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values from 2009 through 2013 (NOAA).  Note the yearly minimum observation is now in the past and we are one month removed from the yearly maximum value.  NOAA is likely to measure this year’s maximum value near 399ppm.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle based on monthly average values.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the recent and ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing of the Earth, which increases the amount of energy in our climate system.

In previous posts on this topic, I showed and discussed historical and projected concentrations at this part of the post.  I will skip this for now because there is something about this data that I think provides a different context of the same conversation.  I saw a graphic last month that I provides useful focus on this topic:

Figure 4 – CO2 concentration (top) and annual average growth rate (bottom). Source: Guardian

The top part of Figure 4 should look familiar – it’s the black line in Figure 3.  The bottom part is the annual change in CO2 concentrations.  If we fit a line to the data, the line would have a positive slope, which means annual changes are increasing with time.  So CO2 concentrations are increasing at an increasing rate – not a good trend with respect to minimizing future warming.  In the 1960s, concentrations increased at less than 1 ppm/year (average rate of increase in the bottom graph by decade).  In the 2000s, concentrations increased at 2.07 ppm/year.  This isn’t surprising – CO2 emissions continue to increase decade after decade.  Natural systems are not equipped to remove CO2 emissions quickly from the atmosphere.  Indeed, natural systems will take tens of thousands of years to remove the CO2 we emitted in the course of a couple short centuries.  Human systems do not yet exist that remove CO2 from any medium (air or water).  They are not likely to exist for some time.  So NOAA will extend the right side of the above graphs for years and decades to come.

The greenhouse effect details how these increasing concentrations will affect future temperatures.  The more GHGs (CO2 and others) are in the atmosphere, all else equal, the more radiative forcing the GHGs cause.  More forcing means warmer temperatures as energy is re-radiated back toward the Earth’s surface.  Conditions higher in the atmosphere affects this relationship, which is what my volcano post addressed.  A number of medium-sized volcanoes injected SO2 into the stratosphere (which is above the troposphere – where we live and our weather occurs) in the last decade.  Those SO2 particles reflected incoming solar radiation.  This happened because of their chemical and radiative properties.  So while we emitted more GHGs into the troposphere, less radiation entered the troposphere (the bottom layer of the atmosphere) in the past 10 years than the previous 10 years.  With less incoming radiation, the GHGs re-emitted less energy toward the surface of the Earth.  This is likely part of the reason why the global temperature trend leveled off in the 2000s after its relatively rapid run-up in previous decades.

This situation is important for the following reason.  Once the SO2 falls out of the atmosphere, the additional incoming radiation will encounter higher GHG concentrations than was present in the late 1990s.  As a result, we will likely see a stronger surface temperature response sometime in the future than the response of the 1990s.

The remainder of the reason is the oceans.  Thanks to the Interdecadal Pacific Oscillation’s most recent negative phase, the Pacific in particular absorbed heat energy near the surface and transported it to the deep ocean instead of allowing the heat to accumulate near the surface.  The following graphic shows how heat absorption by global oceans changed in recent years:

Figure 5. New research that shows anomalous ocean heat energy locations since the late 1950s.  The purple lines in the graph show how the heat content of the whole ocean has changed over the past five decades. The blue lines represent only the top 700 m and the grey lines are just the top 300 m.  Source: Balmaseda et al., (2013)

This temporary energy transport to the deep ocean is good news in the short-term: global surface temperatures slowed their rise during the 2000s compared to the 1990s and 1980s.  That does not mean however the global warming has stopped, as ideological skeptics want you to believe.  That heat energy still exists in the Earth’s climate system.  The oceans move heat around the planet just as the atmosphere does.  The very large amount of extra heat currently in the deep ocean will eventually come back up to the surface.  When it does, it add to the surface warming signal.  So we can expect to see an extra rise of global mean surface temperatures sometime in the future.  Thus, this is not good news in the long-term.

The rise in CO2 concentrations will slow down, stop, and reverse when we decide it will.  It depends primarily on the rate at which we emit CO2 into the atmosphere.  We can choose 350 ppm or 450 ppm or any other target.  That choice is dependent on the type of policies we decide to implement.  It is our current policy to burn fossil fuels because we think doing so is cheap, albeit inefficient and without proper market signals.  We will widely deploy clean sources of energy when they are cheap, the timing of which we control.  We will remove CO2 from the atmosphere when we have cheap and effective technologies and mechanisms to do so, which we also control.  These future trends depend on today’s innovation and investment in research, development, and deployment.  Today’s carbon markets are not the correct mechanism, as they are aptly demonstrating.  We will limit future warming and climate effects when we choose to do so.

March 2013 CO2 Concentrations: 397.34 ppm

During March 2013, the Scripps Institution of Oceanography measured an average of 397.34ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory.

This value is a big deal.  Why?  Because not only is 397.34 ppm the largest CO2 concentration value for any March in recorded history, it is the largest CO2 concentration value in any month in recorded history.  More on that below.  This year’s March value is 2.89 ppm higher than March 2012′s!  Most month-to-month differences are between 1 and 2 ppm.  This jump of 2.89 ppm is very high, but is ~0.5 ppm less than February’s year-over-year change of 3.37 ppm.  Of course, the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below, is more significant.

Let’s get back to that all-time high concentration value.  The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported last year and, prior to the last two months, in recorded history (neglecting proxy data).  We can expect April and May of this year to produce new record values.  I wrote the following two months ago:

If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – this means CO2 concentrations are another climate variable that is increasing faster than experts predicted just a short couple of years ago.

For the most part, I stand by that prediction.  But actual concentration increases might prove  me wrong.  Here is why: the difference in CO2 concentration values between May 2012 and March 2012 was 2.33 ppm (396.78 – 394.45).  If we do the simplest thing and add that same difference to this March’s value, we get 399.67 ppm.  That is awfully close to 400 ppm, but less than the 399.93 ppm extrapolation I performed last month.  I discussed May 2013′s projection with Sourabh after last month’s post.  They predicted 399.5-400 ppm concentration for May 2013.  I think NOAA will measure May 2013′s concentration near 399.3 ppm.  There are other calculations that we could do to come up with a range of predictions, but I unfortunately don’t have the time to do them right now.  I will have content myself with waiting until June to find out how fast concentrations rose through May.

I normally post CO2now.org’s chart of CO2 concentrations since 1958/59 for a given month.  They finally posted last month’s average concentration value yesterday, but have not updated their graph from February 2013 yet.  When they do, I will update this post.

[Update: here is their graphic for March 2013]

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in March from 1958 through 2013.

How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values from 2009 through 2013 (NOAA).  Note the yearly minimum observation is now in the past and we are two months removed from the yearly maximum value.  NOAA is likely to measure this year’s maximum value near 399ppm.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle based on monthly average values.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the recent and ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing of the Earth, which increases the amount of energy in our climate system.

In previous posts on this topic, I showed and discussed historical and projected concentrations at this part of the post.  I will skip this for now because there is something about this data that I think provides a different context of the same conversation.  I saw a graphic last month that I provides useful focus on this topic:

Figure 3 – CO2 concentration (top) and annual average growth rate (bottom). Source: Guardian

The top part of Figure 3 should look familiar – it’s the black line in Figure 3.  The bottom part is the annual change in CO2 concentrations.  If we fit a line to the data, the line would have a positive slope, which means annual changes are increasing with time.  So CO2 concentrations are increasing at an increasing rate – not a good trend with respect to minimizing future warming.  In the 1960s, concentrations increased at less than 1 ppm/year.  In the 2000s, concentrations increased at 2.07 ppm/year.  This isn’t surprising – CO2 emissions continue to increase decade after decade.  Natural systems are not equipped to remove CO2 emissions quickly from the atmosphere.  Indeed, natural systems will take tens of thousands of years to remove the CO2 we emitted in the course of a couple short centuries.  Human systems do not yet exist that remove CO2 from any medium (air or water).  They are not likely to exist for some time.  So NOAA will extend the right side of the above graphs for years and decades to come.

The greenhouse effect details how these increasing concentrations will affect future temperatures.  The more GHGs (CO2 and others) are in the atmosphere, all else equal, the more radiative forcing the GHGs cause.  More forcing means warmer temperatures as energy is re-radiated back toward the Earth’s surface.  Conditions higher in the atmosphere affects this relationship, which is what my volcano post addressed.  A number of medium-sized volcanoes injected SO2 into the stratosphere (which is above the troposphere – where we live and our weather occurs) in the last decade.  Those SO2 particles reflected incoming solar radiation.  So while we emitted more GHGs into the troposphere, less radiation entered the troposphere in the past 10 years than the previous 10 years.  With less incoming radiation, the GHGs re-emitted less energy toward the surface of the Earth.  This is likely part of the reason why the global temperature trend leveled off in the 2000s after its relatively rapid run-up in previous decades.

This situation is important for the following reason.  Once the SO2 falls out of the atmosphere, the additional incoming radiation will encounter higher GHG concentrations than was present in the late 1990s.  As a result, we will likely see a stronger surface temperature response sometime in the future than the response of the 1990s.

The rise in CO2 concentrations will slow down, stop, and reverse when we decide it will.  We can choose 350 ppm or 450 ppm or any other target.  That choice is dependent on the type of policies we decide to implement.  It is our current policy to burn fossil fuels because doing so is cheap, albeit inefficient.  We will widely deploy clean sources of energy when they are cheap, which we control.  We will remove CO2 from the atmosphere when we have cheap and effective technologies and mechanisms to do so, which we control.  Today’s carbon markets are not the correct mechanism, as they are aptly demonstrating.  We will limit future warming and downstream climate effects when we choose to do so.

February 2013 CO2 Concentrations: 396.80 ppm

During February 2013, the Scripps Institution of Oceanography measured an average of 396.80ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory.

This value is a big deal.  Why?  Because not only is 396.80 ppm the largest CO2 concentration value for any February in recorded history, it is the largest CO2 concentration value in any month in recorded history.  More on that below.  This year’s February value is 3.37 ppm higher than February 2012′s!  Most month-to-month differences are between 1 and 2 ppm.  This jump of 3.37 ppm is very high.  Of course, the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below, is more significant.

Let’s get back to that all-time high concentration value.  The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported last year and, prior to this moth, in recorded history (neglecting proxy data).  We can expect March, April, and May of this year to produce new record values.  I wrote the following last month:

If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – this means CO2 concentrations are another climate variable that is increasing faster than experts predicted just a short couple of years ago.

For the most part, I stand by that prediction.  But actual concentration increases might prove  me wrong.  Here is why: the difference in CO2 concentration values between May 2012 and February 2012 was 3.13 ppm (396.78 – 393.65).  If we do the simplest thing and add that same difference to February’s value, we get 399.93 ppm.  That is awfully close to 400 ppm.  A more robust approach would be to add an average value – say the annual growth rate from the past 3, 5, or 10 years.  Over those time periods, the average differences are 2.31 ppm, 2.08 ppm, and 2.08 ppm.  So it’s probably safe to assume a growth of at least 2 ppm, which is what I did in my original prediction.  396.78 ppm + 2 ppm = 398.78 ppm (2013′s prediction).  398.78 ppm + 2 ppm = 400.78 ppm (2014′s prediction).  But if we use annual averages, we smooth out the large jumps in concentration values (like the 2013-2012 February difference).  There are other calculations that we could do to come up with a range of predictions, but I unfortunately don’t have the time to do them right now.  We will have to be content with waiting until early June to find out how fast concentrations are rising this year.

It is worth noting here that stations measured 400ppm CO2 concentration for the first time in the Arctic last year.  The Mauna Loa observations are usually closer to globally averaged values than other sites, such as in the Arctic.  That is why scientists and media reference the Mauna Loa observations most often.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in February: from 1959 through 2012.

This time series chart shows concentrations for the month of January in the Scripps dataset going back to 1959. As I wrote above, concentrations are persistently and inexorably moving upward.  How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values from 2009 through 2013 (NOAA).  Note the yearly minimum observation is now in the past and we are two months removed from the yearly maximum value.  NOAA is likely to measure this year’s maximum value between 398ppm and 399ppm.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle based on monthly average values.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the recent and ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing toward the Earth, which eventually increases tropospheric temperatures.

In previous posts on this topic, I show and discuss historical and projected concentrations at this part of the post.  I will skip this for now because there is something about this data that I think provides a different context of the same conversation.  The increase in average annual concentrations in 2012 generated quite a bit of buzz in media outlets this week.  I dismissed the first couple of reports I saw because I’ve spent so much time during the past year writing about the concentrations.  But more media outlets wrote and discussed the same topic as the week went on.  So I think it is a valid story, especially after I saw a graphic that I thought should have been the focus the entire time:

Figure 4 – CO2 concentration (top) and annual average growth rate (bottom). Source: Guardian

The top part of Figure 4 should look familiar – it’s the black line in Figure 3.  The bottom part is the annual change in CO2 concentrations.  If we fit a line to the data, the line would have a positive slope, which means annual changes are increasing with time.  So CO2 concentrations are increasing at an increasing rate – not a good trend with respect to minimizing future warming.  In the 1960s, concentrations increased at less than 1 ppm/year.  In the 2000s, concentrations increased at 2.07 ppm/year.

The greenhouse effect details how these concentrations will affect future temperatures.  The more GHGs in the atmosphere, all else equal, the more radiative forcing the GHGs cause.  More forcing means warmer temperatures as energy is re-radiated back toward the Earth’s surface.  Conditions higher in the atmosphere affects this relationship, which is what my volcano post addressed.  A number of medium-sized volcanoes injected SO2 into the stratosphere (which is above the troposphere – where we live and our weather occurs).  Those SO2 particles reflect incoming solar radiation.  So while we emitted more GHGs into the troposphere, less radiation entered the troposphere in the past 10 years than the previous 10 years.  With less incoming radiation, the GHGs re-emitted less energy toward the surface of the Earth.  This is likely part of the reason why the global temperature trend leveled off in the 2000s after its run-up in previous decades.

This situation is important for the following reason.  Once the SO2 falls out of the atmosphere, the additional incoming radiation will interact with higher GHG concentrations than was present in the late 1990s.  We will likely see a strong surface temperature response sometime in the future.

In my mind, the newsworthy detail is not that CO2 concentrations increased at the second fastest rate on record in 2012.  In climate, year-to-year differences matter less than long-term trends.  In my mind, the decadal concentration increase is what is noteworthy.  If concentrations rise by an average of >3 ppm/year in the 2010s or 2020s, a great deal of future warming and other climate change effects will occur.

It is my opinion that global temperature rise by 2100 will exceed 2C.  This target is primarily politically-driven.  Scientific research doesn’t exist that dictates 2C is “safe”.  Scientific research does exist that projects the likely temperature response to a range of CO2 concentration values.  If we do want to prevent >2C global temperature rise by 2100, we would have to immediately stop emitting CO2 and begin removing CO2 from the atmosphere.  We currently don’t have technologies to do either.

I have more to say about some details in the Guardian article from which I got Figure 4.  That will have to wait for another post.  The Science study the article mentions is worthy of discussion, as is the Guardian’s comment that concentrations continue to increase despite government action.  The article also links to a recent study of GHG reductions by 2020.  I will address these in an upcoming post.

Weather Extremes and Public Policy

The Philadelphia Inquirer wrote a story yesterday about New Jersey Governor Chris Christie’s choices while the NJ coast is rebuilt post-Sandy.  As a scientist, I agree with other experts that planners need to incorporate climate change projections in their work.  As a scientist transitioning to public policy, I agree with Gov. Christie that the causal link between climate change and Sandy doesn’t matter to victims of the storm in the immediate aftermath.  What does matter?  Today’s infrastructure is clearly not capable of withstanding today’s weather extremes, as Hurricane Katrina and Superstorm Sandy demonstrated.  Both disasters showed it doesn’t matter whether sub-standard infrastructure protects a location (New Orleans) or whether standard or better infrastructure (NY & NJ) does.  The first issue is our standards, not the weather.  The second issue is mitigation and adaptation to a changing climate.

Of course politics are involved.  Gov. Christie’s reelection is this upcoming November.  If victims think their needs are unmet or the NJ coast is not open for tourism this summer, his reelection chances will take a hit.  This political reality will butt up against physical reality.  Sandy occurred in today’s climate.  She wasn’t particularly strong at landfall as hurricanes go in the Atlantic basin (nowhere near Hurricane Katrina or other historic storms).  A unique set of weather events combined to amplify Sandy’s effects.

The mid-20th century buildup of human infrastructure along the coast with minimal consideration of severe weather effects drove Sandy’s costs.  Without buildings abutting the ocean, the storm surge would not have damaged anything but wilderness (which we evidently don’t value).  It is foolish to rebuild buildings  without consideration of today’s severe weather.  It is more foolish to not plan for tomorrow’s climate, but it is Gov. Christie’s prerogative to choose his own vision.  What should planners include?

Proper preparation could mean “hardening” infrastructure (moving power lines underground, for example), forbidding construction in flood zones, modifying building codes, and lifting homes off the ground onto pilings. It could mean relocating people to denser developments that are less flood prone or building sea walls on the coast.

If people want to build in flood zones, the rest of us should not bail them out post-disaster.  Risky behavior requires appropriate responsibility for engaging in that behavior.  Some areas might not be safely inhabitable.  It is the government’s responsibility to determine those areas’ locations and issue building permits and assign zones accordingly.  In addition to sea walls, planners should include natural barriers to storm surge.

If sea level rises an additional four feet off the NJ coast, what are the implications for NJ infrastructure (i.e., risk and cost)?  We build infrastructure to last 100 years, so we should require robust planning and construction.  How many citizens are put at risk with each foot of sea level rise?  Do New Jersey residents want to invest in the near-term to reduce long-term risk or do they want to confront that long-term risk at some undetermined point in the future?  What about the rest of Americans?  Our elected officials decided to spend $60 billion on post-Sandy work.  Is that the best use of that money?  Do we want to spend some of that $60 billion on adaptation measures, and if so how much?

The article includes this (emphasis mine):

Meanwhile, Christie faces pushback from a significant interest group, environmentalists, who want a public planning process to determine the future of the Shore. They want decisions made based on science, not politics.

This is a classic environmentalist complaint.  Every decision includes politics.  Climate science is largely federally funded.  Decision makers are largely politicians.  Zoning is political.  There is no pure aspect of science that can issue a non-political decision.  The appeal to scientific purity is a trait of mainstream environmentalism, but it is just as biased as skeptics’ call for no climate science input into decision-making.  Science describes and politics prescribes.  The two are naturally different and intertwined in our technically advanced society.

January 2013 CO2 Concentrations: 395.55ppm

Up and up the value goes.  The Scripps Institution of Oceanography measured an average of 395.55ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory during January 2013.

395.55ppm is the highest value for January concentrations in recorded history. Last year’s 393.14ppm was the previous highest value ever recorded.  This January’s reading is 2.41ppm higher than last year’s.  This increase is significant.  Of course, more significant is the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below.

The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported last year and in recorded history (neglecting proxy data).  Note that January’s value is only 1.23ppm less than May 2012′s.  If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – this means CO2 concentrations are another climate variable that is increasing faster than experts predicted just a short couple of years ago.

It is worth noting here that stations measured 400ppm CO2 concentration for the first time in the Arctic last year.  The Mauna Loa observations are usually closer to globally averaged values than other sites, such as in the Arctic.  That is why scientists and media reference the Mauna Loa observations most often.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in January: from 1959 through 2012.

This time series chart shows concentrations for the month of January in the Scripps dataset going back to 1959. As I wrote above, concentrations are persistently and inexorably moving upward.  How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values from 2009 through 2013 (NOAA).  Note the yearly minimum observation is now in the past and we are three months removed from the yearly maximum value.  NOAA is likely to measure this year’s maximum value at ~398ppm.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the recent and ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing toward the Earth, which eventually increases lower tropospheric temperatures.

We could instead take a 10,000 year view of CO2 concentrations from ice cores and compare that to the recent Mauna Loa observations.  This allows us to determine how today’s concentrations compare to geologic conditions:

Figure 4 – Historical (10,000 year) CO2 concentrations from ice core proxies (blue and green curves) and direct observations made at Mauna Loa, Hawai’i (red curve) through the early 2000s.

Or we could take a really, really long view into the past:

Figure 5 – Historical record of CO2 concentrations from ice core proxy data, 2008 observed CO2 concentration value, and 2 potential future concentration values resulting from lower and higher emissions scenarios used in the IPCC’s AR4.

Note that this last graph includes values from the past 800,000 years, 2008 observed values (~8-10ppm less than this year’s average value will be) as well as the projected concentrations for 2100 derived from a lower emissions and higher emissions scenarios used by the IPCC’s Fourth Assessment Report from 2007.  Has CO2 varied naturally in this time period?  Of course it has.  But you can easily see that previous variations were between 180 and 280ppm and took thousands of years to move between the two.  In contrast, the concentration has, at no time during the past 800,000 years, risen to the level at which it currently exists; nor has the concentration changed so quickly (287ppm to 395ppm in less than two hundred years!).  That is important because of the additional radiative forcing that increased CO2 concentrations impart on our climate system.  You or I may not detect that warming on any particular day, but we are just starting to feel their long-term impacts.

Moreover, if our current emissions rate continues unabated, it looks like a tripling of average pre-industrial concentrations will be our reality by 2100 (278 *3 = 834).  Figure 5 clearly demonstrates how anomalous today’s CO2 concentration values are (much higher than the average, or even the maximum, recorded over the past 800,000 years).  It further shows how significant the projected emission pathways are.  I will point out that our actual emissions to date are greater than the higher emissions pathway shown above.  That means that if we continue to emit CO2 at an increasing rate, end-of-century concentration values would exceed the value shown in Figure 5 (~1100ppm instead of 800).  This reality will be partially addressed in the upcoming 5th Assessment Report (AR5), currently scheduled for public release in 2013-14.

Given our historical emissions to date and the likelihood that they will continue to grow at an increasing rate for at least the next 25 years, we will pass a number of “safe” thresholds – for all intents and purposes permanently as far as concerns our species. It is time to start seriously investigating and discussing what kind of world will exist after CO2 concentrations peak at 850 or 1200ppm. No knowledgeable body, including the IPCC, has done this to date. To remain relevant, I think institutions who want a credible seat at the climate science-policy table will have to do so moving forward.  The work leading up to AR5 will begin to fill in some of this knowledge gap.  I expect most of that work has recently started and will be available to the public around the same time as the AR5 release.  This could potentially cause some confusion in the public since the AR5 will tell one storyline while more recent research might tell a different storyline.

The fourth and fifth graphs imply that efforts to pin any future concentration goal to a number like 350ppm or even 450ppm will be incredibly difficult – 350ppm more so than 450ppm, obviously. Beyond an education tool, I don’t see the utility in using 350ppm – we simply will not achieve it, or anything close to it, given our history and likelihood that economic growth goals will trump any effort to address CO2 concentrations in the near future (as President Obama himself stated in 2012).  That is not to say that we should abandon hope or efforts to do something.  On the contrary, this series informs those who are most interested in action.  With a solid basis in the science, we become equipped to discuss policy options.  I join those who encourage efforts to tie emissions reductions to economic growth through scientific and technological research and innovation.  This path is the only credible one moving forward.

December 2012 CO2 Concentrations: 394.39ppm

The Scripps Institution of Oceanography measured an average of 394.39ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory during December 2012.

394.39ppm is the highest value for December concentrations in recorded history. Last year’s 391.79ppm was the previous highest value ever recorded.  This December’s reading is 2.60ppm higher than last year’s.  This increase is significant.  Of course, more significant is the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below.

The yearly maximum monthly value normally occurs during May. Last year was no different: the 396.78ppm concentration in May 2012 was the highest value reported this year and in recorded history (neglecting proxy data).  Note that December 2012′s value is only 2.39ppm less than May 2012′s.  If we extrapolate last year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014; I expect May 2013′s value will be ~398ppm).  Note that I previously wrote that this wouldn’t occur until 2015 – another climate variable that is increasing faster than energy or climate experts predicted.

It is worth noting here that stations measured 400ppm CO2 concentration for the first time in the Arctic last year.  The Mauna Loa observations represent more well-mixed (global) conditions while sites in the Arctic and elsewhere more accurately measure local and regional concentrations.  That is why scientists and media reference the Mauna Loa observations most often.

Earlier last year, I predicted that 2012 would not see an average monthly CO2 concentration below 390ppm.  I was correct: September and October 2012 concentration values were the lowest recorded last year (391ppm).  It wasn’t the hardest prediction to make: the trend was going up at a steady rate and based on humanity’s continued reliance on fossil fuels, we weren’t going to break that trend.  The next prediction to verify is the first month at Mauna Loa during which Scripps records an 400ppm average.  After that, the first year during which the minimum concentration is at least 400ppm, which I think will occur within the next 5 years.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in December: from 1958 through 2012.

This time series chart shows concentrations for the month of December in the Scripps dataset going back to 1958. As I wrote above, concentrations are persistently and inexorably moving upward.  How do concentration measurements change in calendar years?  The following two graphs demonstrate this.

Figure 2 – Monthly CO2 concentration values from 2008 through 2013 (NOAA).  Note the yearly minimum observations are now in the past and we are five months removed from the yearly maximum value.

Figure 3 – 50 year time series of CO2 concentrations at Mauna Loa Observatory.  The red curve represents the seasonal cycle.  The black curve represents the data with the seasonal cycle removed to show the long-term trend.  This graph shows the ongoing increase in CO2 concentrations.  Remember that as a greenhouse gas, CO2 increases the radiative forcing toward the Earth, which eventually increases lower tropospheric temperatures.

We could instead take a 10,000 year view of CO2 concentrations from ice cores and compare that to the recent Mauna Loa observations.  This allows us to determine how today’s concentrations compare to geologic conditions:

Figure 4 – Historical (10,000 year) CO2 concentrations from ice core proxies (blue and green curves) and direct observations made at Mauna Loa, Hawai’i (red curve).

Or we could take a really, really long view into the past:

Figure 5 – Historical record of CO2 concentrations from ice core proxy data, 2008 observed CO2 concentration value, and 2 potential future concentration values resulting from lower and higher emissions scenarios used in the IPCC’s AR4.

Note that this last graph includes values from the past 800,000 years, 2008 observed values (~8-10ppm less than this year’s average value will be) as well as the projected concentrations for 2100 derived from a lower emissions and higher emissions scenarios used by the IPCC’s Fourth Asssessment Report from 2007.  Has CO2 varied naturally in this time period?  Of course it has.  But you can easily see that previous variations were between 180 and 280ppm.  In contrast, the concentration has, at no time during the past 800,000 years, risen to the level at which it currently exists.  That is important because of the additional radiative forcing that increased CO2 concentrations impart on our climate system.  You or I may not detect that warming on any particular day, but we are just starting to feel their long-term impacts.

Moreover, if our current emissions rate continues unabated, it looks like a tripling of average pre-industrial concentrations will be our reality by 2100 (278 *3 = 834).  Figure 5 clearly demonstrates how anomalous today’s CO2 concentration values are (much higher than the average, or even the maximum, recorded over the past 800,000 years).  It further shows how significant projected emission pathways are.  I will point out that our actual emissions to date are greater than the higher emissions pathway shown above.  That means that if we continue to emit CO2 at an increasing rate, end-of-century concentration values would exceed the value shown in Figure 5.  This reality will be partially addressed in the upcoming 5th Assessment Report (AR5), currently scheduled for public release in 2013-14.

Given our historical emissions to date and the likelihood that they will continue to grow at an increasing rate for at least the next 25 years, we will pass a number of “safe” thresholds – for all intents and purposes permanently as far as concerns our species. It is time to start seriously investigating and discussing what kind of world will exist after CO2 concentrations peak at 850 or 1200ppm. No knowledgeable body, including the IPCC, has done this to date. To remain relevant, I think institutions who want a credible seat at the climate science-policy table will have to do so moving forward.  The work leading up to AR5 will begin to fill in some of this knowledge gap.  I expect most of that work has recently started and will be available to the public around the same time as the AR5 release.  This could potentially cause some confusion in the public since the AR5 will tell one storyline while more recent research might tell a different storyline.

The fourth and fifth graphs imply that efforts to pin any future concentration goal to a number like 350ppm or even 450ppm will be incredibly difficult – 350ppm more so than 450ppm, obviously. Beyond an education tool, I don’t see the utility in using 350ppm – we simply will not achieve it, or anything close to it, given our history and likelihood that economic growth goals will trump any effort to address CO2 concentrations in the near future (as President Obama himself stated in 2012).  That is not to say that we should abandon hope or efforts to do something.  On the contrary, this series informs those who are most interested in doing something.  With a solid basis in the science, we become well equipped to discuss policy options.  I join those who encourage efforts to tie emissions reductions to economic growth through scientific and technological research and innovation.  This path is the only credible one moving forward.

November 2012 CO2 Concentrations: 392.92ppm

The Scripps Institution of Oceanography measured an average of 392.92ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory during November 2012.

392.92ppm is the highest value for November concentrations in recorded history. Last year’s 390.31ppm was the previous highest value ever recorded.  This November’s reading is 2.61ppm higher than last year’s.  This increase is significant.  Of course, more significant is the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below.

The yearly maximum monthly value normally occurs during May. This year was no different: the 396.78ppm concentration in May 2012 was the highest value reported this year and in recorded history (neglecting proxy data).  If we extrapolate this year’s maximum value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014).  Note that I previously wrote that this wouldn’t occur until 2015 – another climate variable that is increasing faster than energy or climate experts predicted.

I’ve seen comments in the skeptic blogosphere that CO2 measured at Mauna Loa should be higher than anywhere else because of its elevation and specific location.  This is an effort to challenge the credibility of the dataset.  It is important to understand that this statement exists somewhere between correct to purposefully confusing to outright deceitful.  CO2 is a well-mixed constituent of the atmosphere.  That means that emissions of new CO2 are quickly and pretty evenly distributed in space.  While point locations might vary between each other (differences between polar and tropical CO2 concentrations at the same point in time vary the most, for example), the observations at Mauna Loa are very representative of those found across the set of observation stations on the globe.  In addition, as the graphs below will help demonstrate, the historical record is very clear – concentrations have done only one thing in the past 50+ years at any station you want to discuss: increased.  There has been no plateauing or decrease in that time period.

That being said, it is worth noting here that stations measured 400ppm CO2 concentration for the first time in the Arctic earlier this year.  The Mauna Loa observations represent more well-mixed (global) conditions while sites in the Arctic and elsewhere more accurately measure local and regional concentrations.  That is why scientists and media reference the Mauna Loa observations most often.

Earlier in the year, I predicted that 2012 would not see an average monthly CO2 concentration below 390ppm.  It wasn’t the hardest prediction to make: the trend was going up at a steady rate and based on humanity’s continued reliance on fossil fuels, we weren’t going to break that trend this year.  The next prediction to verify is the first month at Mauna Loa during which Scripps records an 400ppm average.  After that, the first year during which the minimum concentration is at least 400ppm, which I think will occur within the next 5 years.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in November: from 1958 through 2012.

This time series chart shows concentrations for the month of November in the Scripps dataset going back to 1958. As I wrote above, concentrations are persistently and inexorably moving upward. Alternatively, we could take a 10,000 year view of CO2 concentrations from ice cores and compare that to the recent Mauna Loa observations:

Figure 2 – Historical (10,000 year) CO2 concentrations from ice core proxies (blue and green curves) and direct observations made at Mauna Loa, Hawai’i (red curve).

Or we could take a really, really long view into the past:

Figure 3 – Historical record of CO2 concentrations from ice core proxy data, 2008 observed CO2 concentration value, and 2 potential future concentration values resulting from lower and higher emissions scenarios used in the IPCC’s AR4.

Note that this graph includes values from the past 800,000 years, 2008 observed values (~6-8ppm less than this year’s average value will be) as well as the projected concentrations for 2100 derived from a lower emissions and higher emissions scenarios used by the IPCC’s Fourth Asssessment Report from 2007.  Has CO2 varied naturally in this time period?  Of course it has.  But you can easily see that previous variations were between 180 and 280ppm.  In contrast, the concentration has, at no time during the past 800,000 years, risen to the level at which it currently exists.  That is important because of the additional radiative forcing that increased CO2 concentrations impart on our climate system.  You or I may not detect that warming on any particular day, but we are just starting to feel their long-term impacts.

Moreover, if our current emissions rate continues unabated, it looks like a tripling of average pre-industrial concentrations will be our reality by 2100 (278 *3 = 834).  This graph clearly demonstrates how anomalous today’s CO2 concentration values are (much higher than the average recorded over the past 800,000 years).  It further shows how significant projected emission pathways are.  I will point out that our actual emissions to date are greater than the higher emissions pathway shown above.  This reality will be partially addressed in the upcoming 5th Assessment Report (AR5), currently scheduled for public release in 2013-14.

Given our historical emissions to date and the likelihood that they will continue to grow at an increasing rate for at least the next 25 years, we will pass a number of “safe” thresholds – for all intents and purposes permanently as far as concerns our species. It is time to start seriously investigating and discussing what kind of world will exist after CO2 concentrations peak at 850 or 1100ppm. No knowledgeable body, including the IPCC, has done this to date. To remain relevant, I think institutions who want a credible seat at the climate science-policy table will have to do so moving forward.  The AR5 might possibly fill in some of this knowledge gap.  I expect most of that work has recently started and will be available to the public around the same time as the AR5 release, which is likely to cause some confusion in the public.

As the second and third graphs imply, efforts to pin any future concentration goal to a number like 350ppm or even 450ppm will be incredibly difficult – 350ppm more so than 450ppm, obviously. Beyond an education tool, I don’t see the utility in using 350ppm – we simply will not achieve it, or anything close to it, given our history and likelihood that economic growth goals will trump any effort to address CO2 concentrations in the near future (as President Obama himself stated recently).  That is not to say that we should abandon hope or efforts to do something.  On the contrary, this series informs those who are most interested in doing something.  With a solid basis in the science, we become well equipped to discuss policy options.  I join those who encourage efforts to tie emissions reductions to economic growth through scientific and technological research and innovation.  This path is the only credible one moving forward.

October 2012 CO2 Concentrations: 391.07ppm

The Scripps Institution of Oceanography measured an average of 391.03ppm CO2 concentration at their Mauna Loa, Hawai’i’s Observatory during October 2012.

391.03ppm is the highest value for October concentrations in recorded history. Last year’s 388.92ppm was the previous highest value ever recorded.  This October’s reading is 2.11ppm higher than last year’s.  This increase is significant.  Of course, more significant is the unending trend toward higher concentrations with time, no matter the month or specific year-over-year value, as seen in the graphs below.

The yearly maximum monthly value normally occurs during May. This year was no different: the 396.78ppm concentration in May 2012 was the highest value reported this year and in recorded history (I’m neglecting proxy data).  If we extrapolate this year’s value out in time, it will only be 2 years until Scripps reports 400ppm average concentration for a singular month (likely May 2014).  Note that I previously wrote that this wouldn’t occur until 2015.  I’ve seen comments on other posts that CO2 measured at Mauna Loa should be higher than anywhere else because of its elevation and specific location.  It is important to understand that this statement exists somewhere between correct to purposefully confusing to outright deceitful.  CO2 is a well-mixed constituent of the atmosphere.  That means that emissions of new CO2 are quickly and pretty evenly distributed in space.  While point locations might vary between each other (differences between polar and tropical CO2 concentrations at the same point in time vary the most, for example), the observations at Mauna Loa are very representative of those found across the set of observation stations on the globe.  In addition, as the graphs below will help demonstrate, the historical record is very clear: concentrations have done only one thing in the past 50+ years at Mauna Loa (or any other station, for that matter): increased.  There has been no plateauing or decrease in that time period.  Moreover, concentrations at all the individual recording sites show the same long-term trend: an increase.

That being said, it is worth noting here that stations measured 400ppm CO2 concentration for the first time in the Arctic earlier this year.  The Mauna Loa observations represent more well-mixed (global) conditions while sites in the Arctic and elsewhere more accurately measure local and regional concentrations.

Judging by the year-over-year increases seen per month in the past 10 years, I predict 2012 will not see an average monthly concentration below 390ppm.  Last year, I predicted that 2011′s minimum would be ~388ppm.  I overestimated the minimum somewhat since both September’s and October’s measured concentrations were just under 389ppm.  So far into 2012, my prediction is holding up.  October’s concentration is typically the smallest of any individual month’s.  We will know for certain next month whether October’s 391.0ppm is the minimum this year or not.

Figure 1 – Time series of CO2 concentrations measured at Scripp’s Mauna Loa Observatory in October: from 1957 through 2012.

This time series chart shows concentrations for the month of October in the Scripps dataset going back to 1957. As I wrote above, concentrations are persistently and inexorably moving upward. Alternatively, we could take a 10,000 year view of CO2 concentrations from ice cores and compare that to the recent Mauna Loa observations:

Figure 2 – Historical (10,000 year) CO2 concentrations from ice core proxies (blue and green curves) and direct observations made at Mauna Loa, Hawai’i (red curve).

Or we could take a really, really long view into the past:

Figure 3 – Historical record of CO2 concentrations from ice core proxy data, 2008 observed CO2 concentration value, and 2 potential future concentration values resulting from lower and higher emissions scenarios used in the IPCC’s AR4.

Note that this graph includes values from the past 800,000 years, 2008 observed values (~6-8ppm less than this year’s average value will be) as well as the projected concentrations for 2100 derived from a lower emissions and higher emissions scenarios used by the IPCC.  Has CO2 varied naturally in this time period?  Of course it has.  But you can easily see that previous variations were between 180 and 280ppm.  In contrast, the concentration has, at no time during the past 800,000 years, risen to the level at which it currently exists.

Moreover, if our current emissions rate continues unabated, it looks like a tripling of average pre-industrial concentrations will be our reality by 2100 (278 *3 = 834).  This graph clearly demonstrates how anomalous today’s CO2 concentration values are (much higher than the average recorded over the past 800,000 years).  It further shows how significant projected emission pathways are.  I will point out that our actual emissions to date are greater than the higher emissions pathway shown above.  This reality will be partially addressed in the upcoming 5th Assessment Report, currently scheduled for public release in 2013-14.

Given our historical emissions to date and the likelihood that they will continue to grow at an increasing rate for at least the next 25 years, we will pass a number of “safe” thresholds – for all intents and purposes permanently as far as concerns our species. It is time to start seriously investigating and discussing what kind of world will exist after CO2 concentrations peak at 850 and 1100ppm. I don’t believe the IPCC or any other knowledgeable body has done this to date. To remain relevant, I think institutions who want a credible seat at the climate science-policy table will have to do so moving forward.  The AR5 might possibly fill in some of this knowledge gap.  I expect most of that work has recently started and will be available to the public around the same time as the AR5 release, which is likely to cause some confusion in the public.

As the second and third graphs imply, efforts to pin any future concentration goal to a number like 350ppm or even 450ppm will be incredibly difficult – 350ppm more so than 450ppm, obviously. Beyond an education tool, I don’t see the utility in using 350ppm – we simply will not achieve it, or anything close to it, given our history and likelihood that economic growth goals will trump any effort to address CO2 concentrations in the near future (as President Obama himself stated recently).  That is not to say that we should abandon hope or efforts to do something.  On the contrary, this post series informs those who are most interested in doing something.  With a solid basis in the science, we become well equipped to discuss policy options.  I join those who encourage efforts to tie emissions reductions to economic growth through scientific and technological research and innovation.  I am convinced that path is the only credible one moving forward.

Call for Climate Change-Policy Paradigm Shift

Nature Climate Change‘s most recent issue included a paper by Kevin Anderson and Alice Bows entitled, “A new paradigm for climate change” [subs. req'd].   Kevin works at the Tyndall Centre for Climate Change Research, School of Mechanical Civil and Aerospace Engineering and Alice works at the Sustainable Consumption Institute, School of Mechanical Civil and Aerospace Engineering, University of Manchester.  The discussion and arguments in the paper aren’t exactly novel if you’ve paid attention to the policy side of the climate change topic but bears examination as much as other works on the climate-policy interface, in which I am very interested.

I think the paper has some serious flaws in its assumptions, which detracts from the policy prescriptions offered.  Prime among the flaws is this:

We urgently need to acknowledge that the development needs of many countries leave the rich western nations with little choice but to immediately and severely curb their greenhouse gas emissions

The latter part of this statement simply will not happen, barring additional severe economic distress.  The first part represents progress from the scientific community: developing nations want and deserve higher living standards, of which energy is a primary input.  But developed nations cannot and will not “immediately and severely curb their greenhouse gas emissions”.  There is a choice that these nations make every day: their own economies will grow and they will do so with the cheapest energy possible.

The U.S. recently achieved something through price signals that scientists and environmentalists have failed to achieve via policy for a generation: a significant reduction in overall CO2 emissions: 7.7% since 2006, the largest reduction of all countries or regions.  This is after Congress failed to get a climate-energy bill passed in 2010.  Why did the decrease occur?  Because old coal-fired plants (the most polluting type) grew much more uneconomical to operate in the past few years compared to natural gas-fired plants.  There is a problem moving forward and that is there is nothing substantially cheaper than natural gas on the scale necessary to further reduce U.S. emissions.  Effectively, there is a new baseline from which the U.S. will operate for the next generation.  But natural gas, as most readers are familiar, still pollutes far more than renewable energy sources.  So U.S. emissions will continue to be quite high and more CO2 will accumulate in the atmosphere.

Despite the early flawed assumption, the papers’ authors quite correctly state the following:

[...]any contextual interpretation of the science demonstrates that the threshold of 2°C [increase in average global temperatures] is no longer viable, at least within orthodox political and economic constraints.  Against this backdrop, unsubstantiated hope leaves such constraints unquestioned, while at the same time legitimizing a focus on increasingly improbable low-carbon futures and underplaying high-emission scenarios.

I have written many times on the false hope that low- and moderate-emission pathways represent (given the unfortunate reality that our actual emissions are on a substantially different orientation) and lamented that even climate scientists misdirected their energies by rarely analyzing high-emission scenarios, thereby depriving policymakers with the required scope of potential futures from which we choose.

The authors do present this somewhat accurate portrayal:

At the same time as climate change analyses are being subverted to reconcile them with the orthodoxy of economic growth, neoclassical economics has evidently failed to keep even its own house in order. This failure is not peripheral. It is prolonged, deep-rooted and disregards national boundaries, raising profound issues about the structures, values and framing of contemporary society.

Rather than demonizing neoclassical economics, the authors should look for opportunities within such a framework that would actually result in emissions reductions.  But the authors’ do identify issues that really do lie at the heart of climate policy: the values of contemporary society.  If those values were more robustly analyzed and respected for what they were as a foundation to climate policy, we would have made meaningful progress on the issue.

The lack of such effort is evident in one of the authors’ concluding paragraphs:

It is in this rapidly evolving context that the science underpinning climate change is being conducted and its findings communicated. This is an opportunity that should and must be grasped. Liberate the science from the economics, finance and astrology, stand by the conclusions however uncomfortable. But this is still not enough. In an increasingly interconnected world where the whole — the system — is often far removed from the sum of its parts, we need to be less afraid of making academic judgements. Not unsubstantiated opinions and prejudice, but applying a mix of academic rigour, courage and humility to bring new and interdisciplinary insights into the emerging era. Leave the market economists to fight among themselves over the right price of carbon — let them relive their groundhog day if they wish. The world is moving on and we need to have the audacity to think differently and conceive of alternative futures.

This thrown gauntlet is full of high-minded rhetoric but short on grasping the realities of the world.  I don’t know of any climate scientist who is afraid of making academic judgements.  But it is folly to accuse skeptics of unsubstantiated opinions and prejudice when advocates for climate activism also display their own set of opinions and prejudice – those opinion and prejudices arise through psychological lenses which themselves are rooted in biological constructs.  Insulting one another has done and will continue to not to anything to solve this problem.  Nobody has the “truth” market cornered.  The “new” paradigm championed by the authors bears remarkable resemblance to other recommendations from legions of climate activists before them.  What has such a stance accomplished?  Emissions continue to grow, concentrations continue to accumulate, temperatures continue to rise, etc.

Many of the same people who rail against unsubstantiated opinions and prejudice also vehemently dismiss new articulated paradigms.  I see nothing in this paper, or many others like it, that advocate for the rapid growth of developing economies based on 21st century technologies and innovations, even though such an effort is clearly needed while developed nations work at finding ways to decarbonize their own economies.  Quite simply, this is the least expensive path forward – it leverages opportunity within the economic framework in which we operate.  It strikes me as senseless to continue the same fight that has not achieved meaningful decarbonization in the last two generations.