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Black carbon

Component of fine particulate matter

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Tihomir Novakov originated the term black carbon in the 1970s, after identifying black carbon as fine particulate matter (PM ≤ 2.5 μm aerodynamic diameter) in aerosols. Aerosol black carbon occurs in several linked forms. Formed through the incomplete combustion of fossil fuels, biofuel, and biomass, black carbon is one of the main types of soot particle in both anthropogenic and naturally occurring soot. As soot, black carbon causes disease and premature death. Because of these human health impacts, many countries have worked to reduce their emissions.

In climatology, aerosol black carbon is a climate forcing agent contributing to global warming. Black carbon warms the Earth by absorbing sunlight and heating the atmosphere and by reducing albedo when deposited on snow and ice (direct effects) and indirectly by interaction with clouds, with the total forcing of 1.1 W/m2. Black carbon stays in the atmosphere for only several days to weeks. In contrast, potent greenhouse gases have longer lifecycles. For example, carbon dioxide (CO2) has an atmospheric lifetime of more than 100 years. The IPCC and other climate researchers have posited that reducing black carbon is one of the easiest ways to slow down short term global warming.

The term black carbon is also used in soil science and geology, referring to deposited atmospheric black carbon or directly incorporated black carbon from vegetation fires. Especially in the tropics, black carbon in soils significantly contributes to fertility as it can absorb important plant nutrients.

In climatology, biochar carbon removal sequesters atmospheric carbon as black carbon to slow global warming.

Overview

Michael Faraday recognized that soot was composed of carbon and that it was produced by the incomplete combustion of carbon-containing fuels. The term black carbon was coined by Serbian physicist Tihomir Novakov, referred to as "the godfather of black carbon studies" by James Hansen, in the 1970s. Smoke or soot was the first pollutant to be recognized as having significant environmental impact yet one of the last to be studied by the contemporary atmospheric research community.

Soot is composed of a complex mixture of organic compounds which are weakly absorbing in the visible spectral region and a highly absorbing black component which is variously called "elemental", "graphitic" or "black carbon". The term elemental carbon has been used in conjunction with thermal and wet chemical determinations and the term graphitic carbon suggests the presence of graphite-like micro-crystalline structures in soot as evidenced by Raman spectroscopy. The term black carbon is used to imply that this soot component is primarily responsible for the absorption of visible light. The term black carbon is sometimes used as a synonym for both the elemental and graphitic component of soot. It can be measured using different types of devices based on absorption or dispersion of a light beam or derived from noise measurements.

Early mitigation attempts

The disastrous effects of coal pollution on human health and mortality in the early 1950s in London led to the UK Clean Air Act 1956. This act led to dramatic reductions of soot concentrations in the United Kingdom which were followed by similar reductions in US cities like Pittsburgh and St. Louis. These reductions were largely achieved by the decreased use of soft coal for domestic heating by switching either to "smokeless" coals or other forms of fuel, such as fuel oil and natural gas. The steady reduction of smoke pollution in the industrial cities of Europe and United States caused a shift in research emphasis away from soot emissions and the almost complete neglect of black carbon as a significant aerosol constituent, at least in the United States.

In the 1970s, however, a series of studies substantially changed this picture and demonstrated that black carbon as well as the organic soot components continued to be a large component in urban aerosols across the United States and Europe which led to improved controls of these emissions. In the less-developed regions of the world where there were limited or no controls on soot emissions the air quality continued to degrade as the population increased. It was not generally realized until many years later that from the perspective of global effects the emissions from these regions were extremely important.

Influence on Earth's atmosphere

Most of the developments mentioned above relate to air quality in urban atmospheres. The first indications of the role of black carbon in a larger, global context came from studies of the Arctic Haze phenomena. Black carbon was identified in the Arctic haze aerosols and in the Arctic snow.

In general, aerosol particles can affect the radiation balance leading to a cooling or heating effect with the magnitude and sign of the temperature change largely dependent on aerosol optical properties, aerosol concentrations, and the albedo of the underlying surface. A purely scattering aerosol will reflect energy that would normally be absorbed by the earth-atmosphere system back to space and leads to a cooling effect. As one adds an absorbing component to the aerosol, it can lead to a heating of the earth-atmosphere system if the reflectivity of the underlying surface is sufficiently high.

Early studies of the effects of aerosols on atmospheric radiative transfer on a global scale assumed a dominantly scattering aerosol with only a small absorbing component, since this appears to be a good representation of naturally occurring aerosols. However, as discussed above, urban aerosols have a large black carbon component and if these particles can be transported on a global scale then one would expect a heating effect over surfaces with a high surface albedo like snow or ice. Furthermore, if these particles are deposited in the snow an additional heating effect would occur due to reductions in the surface albedo.

Measuring and modeling spatial distribution

Levels of black carbon are most often determined based on the modification of the optical properties of a fiber filter by deposited particles. Either filter transmittance, filter reflectance or a combination of transmittance and reflectance is measured. Aethalometers are frequently used devices that optically detect the changing absorption of light transmitted through a filter ticket. The USEPA Environmental Technology Verification program evaluated both the aethalometer and also the Sunset Laboratory thermal-optical analyzer. A multiangle absorption photometer takes into account both transmitted and reflected light. Alternative methods rely on satellite based measurements of optical depth for large areas or more recently on spectral noise analysis for very local concentrations.

In the late 1970s and early 1980s surprisingly large ground level concentrations of black carbon were observed throughout the western Arctic. Modeling studies indicated that they could lead to heating over polar ice. One of the major uncertainties in modeling the effects of the Arctic haze on the solar radiation balance was limited knowledge of the vertical distributions of black carbon.

During 1983 and 1984 as part of the NOAA AGASP program, the first measurements of such distributions in the Arctic atmosphere were obtained with an aethalometer which had the capability of measuring black carbon on a real-time basis. These measurements showed substantial concentrations of black carbon found throughout the western Arctic troposphere including the North Pole. The vertical profiles showed either a strongly layered structure or an almost uniform distribution up to eight kilometers with concentrations within layers as large as those found at ground level in typical mid-latitude urban areas in the United States. The absorption optical depths associated with these vertical profiles were large as evidenced by a vertical profile over the Norwegian arctic where absorption optical depths of 0.023 to 0.052 were calculated respectively for external and internal mixtures of black carbon with the other aerosol components.

Optical depths of these magnitudes lead to a substantial change in the solar radiation balance over the highly reflecting Arctic snow surface during the March–April time frame of these measurements modeled the Arctic aerosol for an absorption optical depth of 0.021 (which is close to the average of an internal and external mixtures for the AGASP flights), under cloud-free conditions. These heating effects were viewed at the time as potentially one of the major causes of Arctic warming trends as described in Archives of Dept. of Energy, Basic Energy Sciences Accomplishments.

Presence in soils

Typically, black carbon accounts for 1 to 6%, and up to 60% of the total organic carbon stored in soils is contributed by black carbon. Especially for tropical soils black carbon serves as a reservoir for nutrients. Experiments showed that soils without high amounts of black carbon are significantly less fertile than soils that contain black carbon. An example of this increased soil fertility is the Terra preta soils of central Amazonia, presumably human-made by pre-Columbian native populations. Terra preta soils have, on average, three times higher soil organic matter (SOM) content, higher nutrient levels, and a better nutrient retention capacity than surrounding infertile soils. In this context, the slash and burn agricultural practice used in tropical regions does not only enhance productivity by releasing nutrients from the burned vegetation but also by adding black carbon to the soil. Nonetheless, for sustainable management, a slash-and-char practice would be better to prevent high emissions of CO2 and volatile black carbon. Furthermore, the positive effects of this type of agriculture are counteracted if used for large patches so that the vegetation does not prevent soil erosion.

Presence in waters

Soluble and colloidal black carbon retained on the landscape from wildfires can make its way to groundwater. On a global scale, the flow of black carbon into fresh and salt water bodies approximates the rate of wildfire black carbon production.

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