Archive for the ‘aerosols’ Category


Natural aerosols, not ‘human pollution’. Another climate assumption gets blown out of the water.
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In addition to oxygen, nitrogen or carbon dioxide, the air we breathe contains small amounts of organic gases, such as benzene and toluene, says Phys.org.

These oxidize into small particles or aerosols that contribute to the condensation of water in the droplets that form clouds.

Now, a study by the Institut de Cièncias del Mar (ICM-CSIC), the Instituto de Química Física Rocasolano (IQFR-CSIC) and the Plymouth Marine Laboratory (PML) stresses the importance of clouds, which filter solar radiation, for understanding past and future climate changes.

“If we don’t get the clouds right, we won’t get the climate right,” says Charel Wohl, ICM-CSIC researcher and lead author of the study. “We are just beginning to unveil the multiple ingredients that form cloud seeds,” he adds.

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It’s ‘study suggests’ time again. NZW: They say (p 4283) it’s a credible hypothesis that global temperature trend changes since 2000 could be “arising largely from internal variability.”
— These results definitely won’t please the climate obsessive tendency.

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A new study by a team of leading climate scientists suggests that the effect of carbon dioxide this century might be small when compared to natural climate variability, says Net Zero Watch.

Global surface temperature is, and always has been, the key climate parameter.

Whatever is happening to the Earth’s climate balance, it must, sooner or later, be reflected in the global annual average temperature, and not just in regional variations.

But therein lies what is to some an inconvenience, as the changes in the global temperature this century is open to differing interpretations including the suggestion that increases in anthropogenic greenhouse gas emissions are not needed to explain the changes we have seen in the last 20 years or so.

It’s a conclusion that many would dismiss as coming from climate “sceptics,” or downright deniers. But what if it’s the view of scientists from two of the world’s leading institutes researching climate change; the University of Oxford and the US National Center for Atmospheric Research. Then it must be taken seriously and not dismissed offhand.

It is important research because it is the trend in the increase of global temperature caused by anthropogenic greenhouse gas emissions that is most important variable for policymakers considering the scale and timescale of action in the coming decades.

However, this vital parameter is uncertain because recent decades have shown that we are living through a period of considerable natural climate variability.

Full article here.

Cumulus clouds over the Atlantic Ocean [image credit: Tiago Fioreze @ Wikipedia]


The article says iodine’s ‘catalytic role in particle formation enhances its effects in the atmosphere wherever it goes, whether that role is eliminating protective ozone molecules or increasing cloud cover.’ But it’s not clear why this claim would be correct: ‘As sea ice melts in the Arctic, more iodine can enter the atmosphere, increase cloud cover and enhance warming effects on the region.’ Effects of cloud cover differ between high and low cloud, for example.
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An international team led by CU Boulder researchers has cracked the chemical code driving the formation of iodine particles in the atmosphere, revealing how the element contributes to increased cloud cover and depletes molecules in the Earth’s protective ozone layer, says Phys.org.

The research, conducted at the world’s largest particle physics laboratory, the European Organization for Nuclear Research (CERN), was published today in the journal Nature Chemistry.

It’s the first time that any experiment in the world has demonstrated the mechanism for how the gas-phase form of iodine—known as iodic acid—forms, and suggests it has an significant role in atmospheric particle formation.

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These researchers seem to have forgotten about the dominant role of water vapour when referring to so-called greenhouse gases – which is odd considering the topic of their study. Are they still promoting an excuse for 1970s cooling?
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Small sulfate particles of diameters 0.4 µm or less from anthropogenic sources could have had a cooling effect on the climate in the 1970s, by triggering cloud formation and reflection radiation, says Hokkaido University (via Phys.org).

Global warming and climate change are one of the most pressing issues of this century.

It is well known that carbon dioxide is the most common greenhouse gas [Talkshop comment – no it isn’t, that’s water vapour by far], but what is less known is that a few anthropogenic aerosols retard the effects of greenhouse gases.

One such chemical is sulfate, which is more infamous for its role in acid rain.

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Layers of Earth’s atmosphere


Q: What could possibly go wrong? A: Even the sky’s not the limit.
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A group of international scientists led by Cornell University is—more rigorously and systematically than ever before—evaluating if and how the stratosphere could be made just a little bit “brighter,” reflecting more incoming sunlight so that an ever-warming Earth maintains its cool, says Phys.org.

Their work is published in the Proceedings of the National Academy of Sciences.

Solar radiation modification—or solar geoengineering, as it is sometimes called—is a potential climate change mitigation strategy that involves injecting sulfate aerosols into the stratosphere, so more sunlight bounces off the Earth’s atmosphere.

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California wildfire [image credit: NASA]


Another day, another topic of model uncertainty. ‘Refining’ an admitted high level of uncertainty is an odd concept, but researchers assert the issue will be ‘cleared up’. However, their belief in ‘potent climate-warming agents’ doesn’t inspire confidence.
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New research refining the amount of sunlight absorbed by black carbon in smoke from wildfires will help clear up a long-time weak spot in earth system models, enabling more accurate forecasting of global climate change, says Phys.org.

“Black carbon or soot is the next most potent climate-warming agent after CO2 and methane, despite a short lifetime of weeks, but its impact in climate models is still highly uncertain,” said James Lee, a climate researcher at Los Alamos National Laboratory and corresponding author of the new study in Geophysical Research Letters on light absorption by wildfire smoke. “Our research will clear up that uncertainty.”

The Los Alamos research resolves a long-time disconnect between the observations of the amount of light absorbed by black carbon in smoke and the amount predicted by models, given how black carbon is mixed with other material such as condensed organic aerosols that are present in plumes.

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