Not exact matches
Another study, published last year in Reviews of Geophysics, lists the man - made
aerosols as coming
from sulfates, nitrate and
black carbon emitted by internal combustion engines, coal - fired power plants, slash - and - burn agricultural practices, and smoke
from cooking.
In the past, numerous studies have identified
black carbon aerosols emitted
from combustion of fossil fuels and residential biofuels as the dominant light - absorbing
aerosol over South Asia.
Black carbon is an
aerosol emitted by incomplete combustion
from vehicles and factories.
The team evaluated simulated cloud fields
from the multi-scale
aerosol - climate model and examined how specific human - caused
aerosols, such as sulfate,
black carbon (soot), and organic
carbon affect those clouds and, in turn, the climate.
The CARES field campaign was designed to increase scientific knowledge about the evolution of
black carbon, primary organic
aerosols (POA), and secondary organic
aerosols (SOA)
from both human - caused and natural (biogenic) sources.
In fact, a subsequent study conducted by Liu et al. (2015) and published in Nature Communications, contrasts the CARES measurements with those obtained
from the 2012 Clean Air for London (ClearfLo) campaign to show that
aerosol coatings influence
black carbon absorption and the form and structural details of the mixing state may be specific to the source and region where the mixing occurs.
Attribution of early 20th century warming requires a more quantitative consideration of all the contributions (e.g. atmospheric
aerosols,
black carbon etc. as well as anthropogenic greenhouse contributions, recovery
from volcanic
aerosols and solar etc.).
The global mean
aerosol radiative forcing caused by the ship emissions ranges
from -12.5 to -23 mW / m ^ 2, depending on whether the mixing between
black carbon and sulfate is included in the model.
The bottom line is that uncertainties in the physics of
aerosol effects (warming
from black carbon, cooling
from sulphates and nitrates, indirect effects on clouds, indirect effects on snow and ice albedo) and in the historical distributions, are really large (as acknowledged above).
As I said to Andy Revkin (and he published on his blog), the additional decade of temperature data
from 2000 onwards (even the AR4 estimates typically ignored the post-2000 years) can only work to reduce estimates of sensitivity, and that's before we even consider the reduction in estimates of negative
aerosol forcing, and additional forcing
from black carbon (the latter being very new, is not included in any calculations AIUI).
Jacobson, M., 2001: Strong radiative heating due to the mixing state of
black carbon in atmospheric
aerosols, Nature, 409:695 - 697; Sato, M. et al., 2003: Global atmospheric
black carbon inferred
from AERONET, Proceedings of the National Academy of Sciences, vol.
PACific Dust EXperiment «The long range transport of dust and anthropogenic
aerosols (e.g,
black carbon, organics and sulfates, and air pollution
from Eurasia, across the Pacific Ocean, into North America is one of the most wide spread and major pollution events on the planet.
BC FF is for
black carbon from fossil fuel and biofuel, POA FF is for primary organic
aerosol from fossil fuel and biofuel, BB is for biomass burning
aerosols and SOA is for secondary organic
aerosols.»
Judith - Apart
from the general anthro vs. natural disussion of sea ice, I'm always wondering: has anyone seriously considered / studied the possible anthropogenic contribution
from NON-CO2 sources (
black carbon soot /
aerosol deposits on the ice surface, increasing the albedo, melting the ice faster in the sun)?
Overall forcing at the TOA is negative averaged over all
aerosols, but significant atmospheric heating and a net positive TOA forcing is possible for
aerosols with a strong
black carbon component, and some of this will eventually be transmitted to the surface despite the reduction in surface insolation
from the light scattering and absorptive properties of the
aerosols.
The latter can be considered in terms of forcings and natural unforced variations.The major positive forcings were those
from GHGs,
black carbon aerosols, and solar irradiance (including its spectral components).
There is one aspect of climate change that is not fully established: the role of
aerosol pollution (aka global dimming)
from mainly
from sulfates and soot (
black carbon and organic
carbon).
Thus Ramanathan and Carmichael find that the net radiative forcing
from aerosols +
black carbon is approximately -1.4 W / m2.
In short, Lindzen's argument is that the radiative forcing
from aerosols is highly uncertain with large error bars, and that they have both cooling (mainly by scattering sunlight and seeding clouds) and warming (mainly by
black carbon darkening the Earth's surface and reducing its reflectivity) effects.
Aerosols, direct and indirect, seems to have gone
from -1.7 to -1.3 W / m2 (not counting
black carbon here).
There is no evidence of regional cooling
from increases in asian
aerosols so it is logical to conclude that
black carbon and sulfates balance out.
Historical emissions of
black and organic
carbon aerosol from energy - related combustion, 1850 — 2000.
As stated earlier, I agree with the point that tropospheric
aerosols from fossil fuels are incredibly bad for human health and other environmental impacts (
black carbon soot, acid rain, radioactive emissions, mercury poisoning), putting us in a situation of damned if we do, damned if we don't.
Truth, you might also want to note that «soil
black carbon» is a completely different beast
from the
aerosol black carbon issue.
For instance, a colleague
from the University of Illinois — Tami Bond — has some of the best information on some types of
aerosols, such as
black carbon.
Organic
carbon aerosol from fossil fuel sources is invariably internally and externally mixed to some degree with other combustion products such as sulphate and
black carbon (e.g., Novakov et al., 1997; Ramanathan et al., 2001b).