Greenhouse Gas

Greenhouse gases (GHGs) is the name given to a number of gases present in the earth's atmosphere which reduce the loss of heat into space and therefore contribute to global temperatures through the greenhouse effect. These gases are essential to maintaining the temperature of the Earth and without them the planet would be so cold as to be uninhabitable.

The most important greenhouse gas is water vapor which creates clouds. The vast bulk of this is produced by the natural process of evaporation of water from the sea. An excess of greenhouse gases can raise the temperature of a planet to lethal levels, as on Venus where the 90 bar partial pressure of carbon dioxide (CO₂) contributes to a surface temperature of about 467 °C (872 °F). Carbon dioxide is produced by many natural and industrial processes, which currently result in CO₂ levels of 380 ppmv in the atmosphere. The reason for such a low level of carbon dioxide is that CO₂ is quickly taken up by plants through photosynthesis and converted into carbohydrates.

Based on ice-core samples and records (see graphs) current levels of CO₂ are approximately 100 ppmv higher than during immediately pre-industrial times, when direct human influence was negligible.

The Greenhouse Effect

Main article: Greenhouse effect

"Greenhouse gases" are essential to maintaining the temperature of the Earth—without them the planet would be so cold as to be uninhabitable.^[1][2]

When sunlight reaches the surface of the Earth, some of it is absorbed and warms the surface. Because the Earth's surface is much cooler than the sun, it radiates energy at much longer wavelengths than the sun does, peaking in the infrared at about 10 µm. The atmosphere absorbs these longer wavelengths more effectively than it does the shorter wavelengths from the sun. The absorption of this longwave radiant energy warms the atmosphere; the atmosphere is also warmed by transfer of sensible and latent heat from the surface.

Greenhouse gases also emit longwave radiation both upward to space and downward to the surface. The downward part of this longwave radiation emitted by the atmosphere is the "greenhouse effect." The term is a misnomer though, as this process is not the mechanism that warms greenhouses.

On earth, the most abundant greenhouse gases are, in order of relative abundance:

• water vapor
• carbon dioxide
• methane
• nitrous oxide
• ozone
• CFCs

The most important greenhouse gases are:

• water vapor, which causes about 36–70 percent of the greenhouse effect on Earth. (Note that clouds typically affect climate differently from other forms of atmospheric water.)
• carbon dioxide, which causes 9–26 percent
• methane, which causes 4–9 percent
• ozone, which causes 3–7 percent

Note that this is a combination of the strength of the greenhouse effect of the gas and its abundance. For example, methane is a much stronger greenhouse gas than CO₂, but present in much smaller concentrations.

It is not possible to state that a certain gas causes a certain percentage of the greenhouse effect, because the influences of the various gases are not additive. (The higher ends of the ranges quoted are for the gas alone; the lower ends, for the gas counting overlaps.)^[3] Other greenhouse gases include, but are not limited to, nitrous oxide, sulfur hexafluoride, hydrofluorocarbons, perfluorocarbons and chlorofluorocarbons (see IPCC list of greenhouse gases). A significant greenhouse gas not yet addressed by the IPCC (or the Kyoto Protocol) is nitrogen trifluoride.^[4]

The major atmospheric constituents (nitrogen, N₂ and oxygen, O₂) are not greenhouse gases. This is because homonuclear diatomic molecules such as N₂ and O₂ neither absorb nor emit infrared radiation, as there is no net change in the dipole moment of these molecules when they vibrate. Molecular vibrations occur at energies that are of the same magnitude as the energy of the photons on infrared light. Heteronuclear diatomics such as CO or HCl absorb IR; however, these molecules are short-lived in the atmosphere owing to their reactivity and solubility. As a consequence they do not contribute significantly to the greenhouse effect.

Late nineteenth-century scientists experimentally discovered that N₂ and O₂ did not absorb infrared radiation (called, at that time, "dark radiation") and that CO₂ and many other gases did absorb such radiation. It was recognized in the early twentieth century that the known major greenhouse gases in the atmosphere caused the earth's temperature to be higher than it would have been without the greenhouse gases.

Natural and anthropogenic

Most greenhouse gases have both natural and anthropogenic sources. During the pre-industrial holocene, concentrations of these gases were roughly constant. Since the industrial revolution, concentrations of all the long-lived greenhouse gases have increased due to human actions.^[2]

Gas	Preindustrial Level	Current Level	Increase since 1750	Radiative forcing (W/m2)
Carbon dioxide	280 ppm	384ppm	104 ppm	1.46
Methane	700 ppb	1,745 ppb	1,045 ppb	0.48
Nitrous oxide	270 ppb	314 ppb	44 ppb	0.15
CFC-12	0	533 ppt	533 ppt	0.17

Ice cores provide evidence for variation in greenhouse gas concentrations over the past 800,000 years. Both CO₂ and CH₄ vary between glacial and interglacial phases, and concentrations of these gases correlate strongly with temperature. Before the ice core record, direct measurements do not exist. Various proxies and modeling suggests large variations; 500 millions years ago CO₂ levels were likely 10 times higher than now.^[5] Indeed higher CO₂ concentrations are thought to have prevailed throughout most of the Phanerozoic eon, with concentrations four to six times current concentrations during the Mesozoic era, and ten to fifteen times current concentrations during the early Palaeozoic era until the middle of the Devonian period, about 400 million years ago.^[6] The spread of land plants is thought to have reduced CO₂ concentrations during the late Devonian, and plant activities as both sources and sinks of CO₂ have since been important in providing stabilizing feedbacks.^[7]

Earlier still, a 200-million year period of intermittent, widespread glaciation extending close to the equator (Snowball Earth) appears to have been ended suddenly, about 550 million years ago, by a colossal volcanic outgassing which raised the CO₂ concentration of the atmosphere abruptly to 12 percent, about 350 times modern levels, causing extreme greenhouse conditions and carbonate deposition as limestone at the rate of about 1mm per day.^[8] This episode marked the close of the Precambrian eon, and was succeeded by the generally warmer conditions of the Phanerozoic, during which multicellular animal and plant life evolved. No volcanic carbon dioxide emission of comparable scale has occurred since. In the modern era, emissions to the atmosphere from volcanoes are only about 1 percent of emissions from human sources.^[8]

Anthropogenic greenhouse gases

Since about 1750, human activity has increased the concentration of carbon dioxide and of some other important greenhouse gases. Natural sources of carbon dioxide are more than 20 times greater than sources due to human activity, but over periods longer than a few years natural sources are closely balanced by natural sinks such as weathering of continental rocks and photosynthesis of carbon compounds by plants and marine plankton. As a result of this balance, the atmospheric concentration of carbon dioxide remained between 260 and 280 parts per million for the 10,000 years between the end of the last glacial maximum and the start of the industrial era.^[9]

Some of the main sources of greenhouse gases due to human activity include:

• burning of fossil fuels and deforestation leading to higher carbon dioxide concentrations. Land use change (mainly deforestation in the tropics) account for up to one-third of total anthropogenic CO₂ emissions.^[9]

• livestock enteric fermentation and manure management,^[10] paddy rice farming, land use and wetland changes, pipeline losses, and covered vented landfill emissions leading to higher methane atmospheric concentrations. Many of the newer style fully vented septic systems that enhance and target the fermentation process also are sources of atmospheric methane.
• use of chlorofluorocarbons (CFCs) in refrigeration systems, and use of CFCs and halons in fire suppression systems and manufacturing processes.
• agricultural activities, including the use of fertilizers, that lead to higher nitrous oxide concentrations.

The seven sources of CO₂ from fossil fuel combustion are (with percentage contributions for 2000–2004):^[11]

1. Solid fuels (e.g. coal): 35 percent
2. Liquid fuels (e.g. gasoline): 36 percent
3. Gaseous fuels (e.g. natural gas): 20 percent
4. Flaring gas industrially and at wells: <1 percent
5. Cement production: 3 percent
6. Non-fuel hydrocarbons: <1 percent
7. The "international bunkers" of shipping and air transport not included in national inventories: 4 percent

The U.S. EPA ranks the major greenhouse gas contributing end-user sectors in the following order: industrial, transportation, residential, commercial, and agricultural.^[12] Major sources of an individual's GHG include home heating and cooling, electricity consumption, and transportation. Corresponding conservation measures are improving home building insulation, compact fluorescent lamps and choosing energy-efficient vehicles.

Carbon dioxide, methane, nitrous oxide and three groups of fluorinated gases (sulfur hexafluoride, HFCs, and PFCs) are the major greenhouse gases and the subject of the Kyoto Protocol, which came into force in 2005.^[13]

Although CFCs are greenhouse gases, they are regulated by the Montreal Protocol, which was motivated by CFCs' contribution to ozone depletion rather than by their contribution to global warming. Note that ozone depletion has only a minor role in greenhouse warming though the two processes often are confused in the media.

Role of water vapor

Water vapor is a naturally occurring greenhouse gas and accounts for the largest percentage of the greenhouse effect, between 36 percent and 66 percent.^[3] Water vapor concentrations fluctuate regionally, but human activity does not directly affect water vapor concentrations except at local scales (for example, near irrigated fields).

The Clausius-Clapeyron relation establishes that warmer air can hold more water vapor per unit volume. Current state-of-the-art climate models predict that increasing water vapor concentrations in warmer air will amplify the greenhouse effect created by anthropogenic greenhouse gases while maintaining nearly constant relative humidity. Thus water vapor acts as a positive feedback to the forcing provided by greenhouse gases such as CO₂.^[14]

Greenhouse gas emissions

Measurements from Antarctic ice cores show that just before industrial emissions started, atmospheric CO₂ levels were about 280 parts per million by volume (ppm; the units µL/L are occasionally used and are identical to parts per million by volume). From the same ice cores it appears that CO₂ concentrations stayed between 260 and 280 ppm during the preceding 10,000 years. However, because of the way air is trapped in ice and the time period represented in each ice sample analyzed, these figures are long term averages not annual levels. Studies using evidence from stomata of fossilized leaves suggest greater variability, with CO₂ levels above 300 ppm during the period 7,000–10,000 years ago,^[15] though others have argued that these findings more likely reflect calibration/contamination problems rather than actual CO₂ variability.^[16]

Since the beginning of the Industrial Revolution, the concentrations of many of the greenhouse gases have increased. The concentration of CO₂ has increased by about 100 ppm (i.e., from 280 ppm to 380 ppm). The first 50 ppm increase took place in about 200 years, from the start of the Industrial Revolution to around 1973; the next 50 ppm increase took place in about 33 years, from 1973 to 2006.^[17]. Many observations are available online in a variety of Atmospheric Chemistry Observational Databases. The greenhouse gases with the largest radiative forcing are:

Relevant to radiative forcing

Gas	Current (1998) Amount by volume	Increase over pre-industrial (1750)	Percentage increase	Radiative forcing (W/m²)
Carbon dioxide	365 ppm {383 ppm(2007.01)}	87 ppm {105 ppm(2007.01)}	31% {37.77%(2007.01)}	1.46 {~1.532 (2007.01)}
Methane	1,745 ppb	1,045 ppb	150%	0.48
Nitrous oxide	314 ppb	44 ppb	16%	0.15

Relevant to both radiative forcing and ozone depletion; all of the following have no natural sources and hence zero amounts pre-industrial

Gas	Current (1998) Amount by volume	Radiative forcing (W/m²)
CFC-11	268 ppt	0.07
CFC-12	533 ppt	0.17
CFC-113	84 ppt	0.03
Carbon tetrachloride	102 ppt	0.01
HCFC-22	69 ppt	0.03

(Source: IPCC radiative forcing report 1994 updated (to 1998).)

Recent rates of change and emission

The sharp acceleration in CO₂ emissions since 2000 of >3% y⁻¹ (>2 ppm y⁻¹) from 1.1% y⁻¹ during the 1990s is attributable to the lapse of formerly declining trends in carbon intensity of both developing and developed nations. Although over 3/4 of cumulative anthropogenic CO₂ is still attributable to the developed world, China was responsible for most of global growth in emissions during this period. Localized plummeting emissions associated with the collapse of the Soviet Union have been followed by slow emissions growth in this region due to more efficient energy use, made necessary by the increasing proportion of it that is exported.^[11] In comparison, methane has not increased appreciably, and N₂O by 0.25% y⁻¹.

The direct emissions from industry have declined due to a constant improvement in energy efficiency, but also to a high penetration of electricity. If one includes indirect emissions, related to the production of electricity, CO₂ emissions from industry in Europe are roughly stabilized since 1994.

Asia

Atmospheric levels of CO₂ have set another new peak, partly a sign of the industrial rise of Asian economies led by China. China is expected to continue to increase its carbon dioxide emissions, largely because of the rapid construction of old-fashioned power plants in poorer internal provinces.

United States

According to a preliminary estimate by the Netherlands Environmental Assessment Agency, the largest national producer of CO₂ emissions since 2006 has been China with an estimated annual production of about 6200 megatonnes. China is followed by the United States with about 5,800 megatonnes. However the per capita emission figures of China are still about one quarter of those of the US population.

Relative to 2005, China's fossil CO₂ emissions increased in 2006 by 8.7 percent, while in the USA, comparable CO₂ emissions decreased in 2006 by 1.4 percent. The agency notes that its estimates do not include some CO₂ sources of uncertain magnitude.^[18] These figures rely on national CO₂ data that do not include aviation. Although these tonnages are small compared to the CO₂ in the Earth's atmosphere, they are significantly larger than pre-industrial levels.

Long-term trend

Atmospheric carbon dioxide concentration is increasing at an increasing rate. In the 1960s, the average annual increase was only 37 percent of what it was in 2000 through 2007.^[19]

Removal from the atmosphere and global warming potential

Aside from water vapor, which has a residence time of days, it is believed that most greenhouse gases take many years to leave the atmosphere.

Greenhouse gases can be removed from the atmosphere by various processes:

• as a consequence of a physical change (condensation and precipitation remove water vapor from the atmosphere).
• as a consequence of chemical reactions within the atmosphere. This is the case for methane. It is oxidized by reaction with naturally occurring hydroxyl radical, OH• and degraded to CO₂ and water vapor at the end of a chain of reactions (the contribution of the CO₂ from the oxidation of methane is not included in the methane Global warming potential). This also includes solution and solid phase chemistry occurring in atmospheric aerosols.
• as a consequence of a physical interchange at the interface between the atmosphere and the other compartments of the planet. An example is the mixing of atmospheric gases into the oceans at the boundary layer.
• as a consequence of a chemical change at the interface between the atmosphere and the other compartments of the planet. This is the case for CO₂, which is reduced by photosynthesis of plants, and which, after dissolving in the oceans, reacts to form carbonic acid and bicarbonate and carbonate ions (see ocean acidification).
• as a consequence of a photochemical change. Halocarbons are dissociated by UV light releasing Cl• and F• as free radicals in the stratosphere with harmful effects on ozone (halocarbons are generally too stable to disappear by chemical reaction in the atmosphere).
• as a consequence of dissociative ionization caused by high energy cosmic rays or lightning discharges, which break molecular bonds. For example, lightning forms N anions from N₂ which then react with O₂ to form NO₂.

Atmospheric lifetime

Jacob (1999)^[20] defines the lifetime ${\displaystyle \tau }$ of an atmospheric species X in a one-box model as the average time that a molecule of X remains in the box. Mathematically ${\displaystyle \tau }$ can be defined as the ratio of the mass ${\displaystyle m}$ (in kg) of X in the box to its removal rate, which is the sum of the flow of X out of the box ( ${\displaystyle F_{out}}$), chemical loss of X ( ${\displaystyle L}$), and deposition of X ( ${\displaystyle D}$) (all in kg/sec): ${\displaystyle \tau ={\frac {m}{F_{out}+L+D}}}$ ^[20]

The atmospheric lifetime of a species therefore measures the time required to restore equilibrium following an increase in its concentration in the atmosphere. Individual atoms or molecules may be lost or deposited to sinks such as the soil, the oceans and other waters, or vegetation and other biological systems, reducing the excess to background concentrations. The average time taken to achieve this is the mean lifetime. The atmospheric lifetime of CO₂ is often incorrectly stated to be only a few years because that is the average time for any CO₂ molecule to stay in the atmosphere before being removed by mixing into the ocean, photosynthesis, or other processes. However, this ignores the balancing fluxes of CO₂ into the atmosphere from the other reservoirs. It is the net concentration changes of the various greenhouse gases by all sources and sinks that determines atmospheric lifetime, not just the removal processes.

Examples of the atmospheric lifetime and GWP for several greenhouse gases include:

• CO₂ has a variable atmospheric lifetime, and cannot be specified precisely.^[9] Recent work indicates that recovery from a large input of atmospheric CO₂ from burning fossil fuels will result in an effective lifetime of tens of thousands of years.^[21] Carbon dioxide is defined to have a GWP of 1 over all time periods.
• Methane has an atmospheric lifetime of 12 ± 3 years and a GWP of 62 over 20 years, 23 over 100 years and 7 over 500 years. The decrease in GWP associated with longer times is associated with the fact that the methane is degraded to water and CO₂ by chemical reactions in the atmosphere.
• Nitrous oxide has an atmospheric lifetime of 120 years and a GWP of 296 over 100 years.
• CFC-12 has an atmospheric lifetime of 100 years and a GWP of 10600 over 100 years.
• HCFC-22 has an atmospheric lifetime of 12.1 years and a GWP of 1700 over 100 years.
• Tetrafluoromethane has an atmospheric lifetime of 50,000 years and a GWP of 5700 over 100 years.
• Sulfur hexafluoride has an atmospheric lifetime of 3,200 years and a GWP of 22000 over 100 years.

Source: IPCC, table 6.7.

The use of CFC-12 (except some essential uses) has been phased out due to its ozone depleting properties^[22]. The phasing-out of less active HCFC-compounds will be completed in 2030.

Airborne fraction

Airborne fraction (AF) is the proportion of an emission (e.g. CO₂) remaining in the atmosphere after a specified time. Canadell (2007)^[23] define the annual AF as the ratio of the atmospheric CO₂ increase in a given year to that year’s total emissions, and calculate that of the average 9.1 PgC y^-1 of total anthropogenic emissions from 2000 to 2006, the AF was 0.45. For CO₂ the AF over the last 50 years (1956-2006) has been increasing at 0.25±0.21%/year.^[23]

Global warming potential

The global warming potential (GWP) depends on both the efficiency of the molecule as a greenhouse gas and its atmospheric lifetime. GWP is measured relative to the same mass of CO₂ and evaluated for a specific timescale. Thus, if a molecule has a high GWP on a short time scale (say 20 years) but has only a short lifetime, it will have a large GWP on a 20 year scale but a small one on a 100 year scale. Conversely, if a molecule has a longer atmospheric lifetime than CO₂ its GWP will increase with time.

Related effects

Carbon monoxide has an indirect radiative effect by elevating concentrations of methane and tropospheric ozone through scavenging of atmospheric constituents (e.g., the hydroxyl radical, OH) that would otherwise destroy them. Carbon monoxide is created when carbon-containing fuels are burned incompletely. Through natural processes in the atmosphere, it is eventually oxidized to carbon dioxide. Carbon monoxide has an atmospheric lifetime of only a few months^[24] and as a consequence is spatially more variable than longer-lived gases.

Another potentially important indirect effect comes from methane, which in addition to its direct radiative impact also contributes to ozone formation. Shindell et al. (2005)^[25] argue that the contribution to climate change from methane is at least double previous estimates as a result of this effect.^[26]

See also

• Atmospheric chemistry
• Carbon dioxide
• Earth's atmosphere
• Global warming
• Greenhouse effect

Notes

References

ISBN links support NWE through referral fees

• Jacob, Daniel. Introduction to Atmospheric Chemistry. Princeton, NJ: Princeton University Press, 1999. ISBN 0691001855
• Lerner, K. Lee, and Brenda Wilmoth Lerner. Environmental issues: essential primary sources. Detroit, MI: Thomson Gale, 2006. ISBN 978-1414406251
• Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M. Tignor, and H.L. Miller (eds.). Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge, UK: Cambridge University Press, 2007. ISBN 978-0521880091

External links

All links retrieved September 24, 2022.

• The NOAA Annual Greenhouse Gas Index (AGGI) Earth System Research Laboratory
• Energy and the environment explained: Greenhouse gases and the climate EIA
• Methane bubbles climate trouble BBC News
• Environmental Effects of Increased Atmospheric Carbon Dioxide Petition Project

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