Science Watch® - Tracking Trends and Performance in Basic Research
September/October 2002



 Lofty Achievement: NOAA’s Susan Solomon on Atmospheric Chemistry

GO TO: The Interviews Before global warming was a frequent feature in newspapers around the world, there was ozone depletion and the Antarctic ozone hole. It was first reported by British scientists in 1985, and the depletion grew so quickly that the researchers who recorded the data assumed at first that their equipment had malfunctioned. The ozone hole was the first great demonstration of humanity's ability to affect our environment on a global scale. But the scientific community responded to the challenge. By 1987, the chemical culprits had been identified—chlorine-containing compounds known as chlorofluorocarbons or CFCs—and world leaders had already mobilized and signed the Montreal Protocol, restricting production and use of CFCs and allowing the process of atmospheric repair to begin.

The discovery of ozone depletion and the response of the scientific community constitutes nothing less than a "scientific success story," in the words of Susan Solomon, a senior scientist at the National Oceanic and Atmospheric Administration in Boulder, Colorado. And it was a story that has resonated down through the decade that followed, in part because of the revelations on how surface chemistry in clouds could have such a dramatic impact on the atmosphere. Indeed, on the basis of her research into the role of chemistry in ozone depletion, Solomon herself was among the most-cited Earth scientists in the 1990s, according to a 2001 Science Watch survey based on ISI Essential Science Indicators Web product (see Science Watch, 12[6]:1-2 November/December 2001). Solomon's seminal 1986 paper "On the depletion of Antarctic ozone" (Nature, 321[6072]:755-758, 1986) has been cited more than 500 times, while 10 more of Solomon papers have been cited well over 100 times each.

Solomon, now 46, received her bachelor's degree in chemistry in 1977 at the Illinois Institute of Technology. She received her Master's and Ph.D. in chemistry from the University of California at Berkeley and then, in 1981, joined the Aeronomy Laboratory at NOAA. In 1992 Solomon was elected to the National Academy of Sciences, becoming its youngest member at that time, and, two years ago, was awarded the National Medal of Science for her remarkable research accomplishments.

From her office in Boulder, Solomon spoke to Science Watch correspondent Gary Taubes.

What was it about the ozone hole that prompted you to drop what you were doing and delve into ozone-depletion research? And was it a quick decision or one you had to think about for awhile?

Prior to the discovery of the ozone hole, my work really focused on what you might call more esoteric aspects of understanding the atmosphere. I was doing atmospheric chemistry, looking at things like the impact of the aurora on the chemistry of the mesosphere, thermosphere, and stratosphere. I was initially reluctant to get involved in the ozone-depletion issue because I viewed the uncertainties as being so huge. In the early days, they were talking about a small percent change over the course of a coming century. That seemed far off and uncertain, and didn't really attract my interest. Then the ozone hole was discovered, and that changed everything. All of a sudden we weren't talking about 5% over a century—we were now talking about 50%. I think it's hard for people not in the field to appreciate the shock value that the discovery really had on the entire community involved in anything related to atmospheric chemistry.

So how did you personally approach the problem?

I was intrigued by the observation, and one of the first things I thought about, coming from this mesosphere/thermosphere kind of work, was whether reactive nitrogen from phenomena like solar protons could be responsible. I convinced myself, however, that that hypothesis didn't fit the data. So then I thought about what could be producing this kind of effect, and I began to wonder whether surface reactions on polar stratospheric cloud surfaces could be the cause. There had already been satellite measurements of these "scientific curiosities" called polar stratospheric clouds. The ozone changes of the Antarctic weren’t being seen in the Arctic, and of course the Antarctic is much colder than the Arctic. So there are a lot more of these funny clouds there. No one ever imagined that surface chemistry could seriously impact the stratosphere. I started imagining ways in which one could make chlorine chemistry much more effective through reactions on those clouds. I ended up proposing in my Nature paper that a reaction between HCl and chlorine nitrate could be occurring on the surfaces of polar stratospheric clouds. That reaction doesn't happen in the gas phase. It happens quite readily on surfaces due to the incorporation of HCl into the surface. Then the chlorine nitrate comes along and you get a reaction occurring in a completely different phase that is quite fast. So that was my proposal in the paper. And it turned out to be the right answer.

"A molecule that can outlast the pyramids of Egypt might be one to think about venting to the atmosphere especially carefully," says the NOAA’s Susan Solomon, of perfluorinated chemicals. "They may as well be immortal."

I also got involved in the observational side of the issue because I strongly argued, along with some other people, including Bob Watson, that we ought to go to the Antarctic and make some measurements to figure out what's going on. It's one thing to see the ozone drop. It's another thing to measure the chemicals that actually influence ozone and to be able to make a science-based statement about why it's changing, whatever that would be. I argued that we ought to have a ground-based expedition to Antarctica, and I was fortunate enough to lead that in 1986 and again in 1987. I was also incredibly fortunate in that two of my colleagues in the Aeronomy Laboratory had designed and built a very high-quality, extremely sensitive instrument for measuring the intensity of incoming light in the visible region of the spectrum. But neither person was available to take the instrument to the Antarctic. I was, and I realized we could measure ozone with it—and also nitrogen dioxide and chlorine dioxide, if it was there. And chlorine dioxide turned out to be there in huge amounts. So we made some of the first measurements of the chemicals that showed what caused the ozone hole.

In the past decade, ozone depletion has been overshadowed, at least in the media, by the global warming issue. Can you update us on what's been happening?

The reason you don't see a lot of press about the ozone hole anymore is that it's really a scientific success story. First there was this incredible observation. Then there was quick action on the part of a lot of people, including myself, to go down there, take the necessary measurements, and figure out what was going on. We had the ground-based expedition in 1986, followed by the airborne expedition by NASA in 1987. They made wonderful measurements of a whole bunch of things. What was fortunate was that when the ozone hole was discovered, the atmospheric chemistry community had the tools to go down there and, in just a couple of years, make enough measurements to prove what was going on. It was a tremendous success. The science fed into quick international regulations to reduce emissions of ozone-damaging chemicals. So now we're in a situation where the science has helped inform a policy action, and the atmosphere is starting very, very slowly to respond. We always knew the response would be slow because the lifetime of these CFCs, once they're put in the atmosphere, is 50 to 500 years. So that means that ozone is just not newsworthy anymore, and that's not a bad thing. That's illustrative of real success.

Can we see an improvement in the ozone layer yet?


Most-Cited Papers by Susan Solomon
Published since 1992

(Ranked by total citations)

Rank Paper Total
Citations
1 D.R. Hanson, A.R. Ravishankara, S. Solomon, "Heterogeneous reactions in sulfuric-acid aerosols: a framework for model calculations," J. Geophys. Res.-Atmospheres, 99(D2):3615-29, 1994. 167
2 S. Solomon, R.R. Garcia, A.R. Ravishankara, "On the role of iodine in ozone depletion," J. Geophys. Res.-Atmospheres, 99(D10):20491-9, 1994. 157
3 R.R. Garcia, S. Solomon, "A new numerical model of the middle atmosphere. 2. Ozone and related species," J. Geophys. Res.-Atmospheres, 99(D6):12937-51, 1994. 149
4 A.R. Ravishankara, et al., "Atmospheric lifetimes of long-lived halogenated species," Science, 259(5092):194-9, 1993. 142
5 S. Solomon, et al., "The role of aerosol variations in anthropogenic ozone depletion at northern midlatitudes," J. Geophys. Res.-Atmospheres, 101(D3):6713-27, 1996. 114

SOURCE: ISI's Web of Science, 1991- 2002

No. But you don’t expect it to happen very quickly because the lifetimes of these CFCs are so long. But at least it's not getting any worse. It will take at least a decade to get better in any kind of obvious way, and that's not exactly Good Morning America type of news. It also doesn't mean the problem would have automatically fixed itself. It simply means the public attention span has been exhausted. And maybe it should be. There are still press statements that come out every year reporting on the size of the ozone hole. Last year was the third-largest ozone hole on record, depending on how you measure it. But that's what we expect. It's going to be in this quasi-stable state—slowly, slowly getting better for a long time to come.

It's interesting to draw a contrast between that history and global warming. For one thing, with global warming the effects so far are smaller relative to the variability. They are now just coming out of the noise level in the last decade or so. And we are just starting to have the tools to measure all the kinds of things we need to measure to fully understand what's going on. The ozone hole, in comparison, was focused and readily accessible to measurement. With global warming, you have to talk about clouds on a global basis; tropospheric water vapor on a global basis—a lot of things that are not easy to measure and have to be done globally, not locally. You just can't do that quickly because it is a global problem.

You said earlier that you didn't take ozone depletion that seriously at first because the effect was so small and the uncertainties so great. Isn't that still the case with global warming and the question of whether it's naturally occurring or anthropogenic?

That's a little bit different. I think you could have made some of the same arguments in the mid-1980s about global warming, but when you look at the decade of the 1990s in particular, the warming was quite remarkable. Global warming, at this time, has turned the corner on detectability. Not as dramatically as the ozone hole did. It wasn't like, all of a sudden—boom—it's huge. But over the last two decades, we have seen an incredible change in temperature, to the point where personally I am becoming convinced that there is a real signal there in the global mean. Another thing to bear in mind in the case of global warming is that you actually have a longer record to compare against. Even without dealing with ice cores and tree rings, you can easily go back to the 1800s. If you include ice cores and tree rings, you can make reasonable estimates back 1,000 years. So we know more about the long-term variability in temperature. And temperature is just much easier to quantify and measure than is ozone. And fortunately, nature has recorded the temperature information for us, and for a lot longer. All those factors have to be in mind when you look at the global warming issue. When you put it all together, the case for a detectable climate signal due to, or likely due to, human activities over the past decades is pretty good. It wouldn't have been good before that.

You left ozone behind in the early 1990s. What have you been concentrating on since then?

What I did for the next few years was to show, in a manner somewhat similar to the polar stratospheric clouds, that other kinds of surfaces could also enhance ozone depletion at lower latitudes. We were able to show, for instance that when El Chichon went off in 1981 and then Pinatubo in the 1990s, both had significant effects on the ups and downs of ozone depletion. Pinatubo, in particular, had a measurable effect in the northern mid-latitude depletion via chlorine chemistry on the volcanic particle surfaces in the stratosphere. That was a pretty major finding and really helped to explain why, at that time of history, the ozone in our latitudes looked the way it did.

I have also done some work on the issue of gases other than carbon dioxide that could contribute to global warming. This has been fascinating from the chemistry point of view. Among other things, one question my colleagues and I have probed is the role of perfluorinated chemicals like CF4, SF6, and others. There’s not a lot of that stuff in the atmosphere today, so I’m not saying they are significant contributors to today’s global warming. But we’ve shown that these molecules live for literally thousands of years—they may as well be immortal—and they are potent absorbers of infrared light, hence greenhouse gases. A molecule that can outlast the pyramids of Egypt might be one to think about venting to the atmosphere especially carefully. In fact, maybe one of the most interesting overlaps between ozone depletion and climate change is that the ozone-depletion issue shows the need for science to help understand not just impacts but also time scales in environmental problems. It’s all part of using science to help inform society about the questions that have to be asked—not just what is or may be happening now, but if something does happen tomorrow, how long will we have to live with it? Particularly if that something tomorrow might possibly be worse than what we are predicting. In the case of the Antarctic ozone hole, the chlorofluorocarbon-induced depletion was far greater than we had predicted, because we didn’t know about surface chemistry. But we knew all along that if ozone depletion did occur, it would last 50 to 100 years, because that’s how long the CFCs last in the atmosphere. As we think about the possibility of future climate change, I think it’s important to think about chemistry, and about the lifetimes of the things that could contribute to the climate. Carbon dioxide lives about 150 years in the atmosphere, so that fact should be part of a science-based risk assessment. Climate change is a complex problem, and this kind of scientific information is one piece of the problem.

In the past five years, I've taken a change of direction doing work more related to understanding how various molecules in the lower atmosphere actually absorb incoming sunlight. It's relevant to the climate problem, but it really addresses the fundamentals of how the system works. So I'm moving into an area that is related to the climate problem, but a little more esoteric. I'm coming back to something like my early work on auroras and things like that, helping to lay the basis for understanding how radiation propagates—how sunlight really gets in through the atmosphere. It isn't front-page New York Times kind of work. That's fine with me. I love doing it. Although I wasn't looking for headlines when we did the ozone work, either. It just kind of fell my way.End

Science Watch®, September/October 2002, Vol. 13, No. 5
Citing URL: http://www.sciencewatch.com/sept-oct2002/sw_sept-oct2002_page3.htm

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