Greenhouse Gas
From ClimateWiki
A greenhouse gas (sometimes abbreviated GHG) is a gas in an atmosphere that absorbs and emits radiation within the thermal infrared range. This process is the fundamental cause of the greenhouse effect. The primary greenhouse gases in the Earth's atmosphere are water vapor, carbon dioxide, methane, nitrous oxide, and ozone. In the Solar System, the atmospheres of Venus, Mars, and Titan also contain gases that cause greenhouse effects. Greenhouse gases greatly affect the temperature of the Earth; without them, Earth's surface would be on average about 33 °C (59 °F) colder than at present.
Since the beginning of the Industrial revolution, the burning of fossil fuels has contributed to the increase in carbon dioxide in the atmosphere from 280ppm to 390ppm. Unlike other pollutants, carbon dioxide emissions do not result from inefficient combustion: CO2 is a product of ideal, stoichiometric combustion of carbon. The emissions of carbon are directly proportional to energy consumption.
Contents |
Greenhouse effects in Earth's atmosphere
Reducing our so-called “Carbon Footprint” by encouraging renewable energy and restricting fossil fuel development makes no sense when the actual composition of the greenhouse is considered. This 1 page graphic shows that water vapor is the overwhelming predominant component of our vital protective greenhouse envelope. Far from being detrimental, greenhouse gases retain the sun’s radiant heat and keep planet Earth from becoming frozen and uninhabitable. Despite the science that contradicts them, the so-called “warmists” contend that man’s CO2 emissions are somehow harmful to our existence. This pictorial representation of the greenhouse envelope clearly demonstrates that man-made CO2 emissions are relatively so tiny that they are of negligible impact and must be viewed accordingly.
In order, the most abundant greenhouse gases in Earth's atmosphere are:
- water vapor
- carbon dioxide
- methane
- nitrous oxide
- ozone
- chlorofluorocarbons
The contribution to the greenhouse effect by a gas is affected by both the characteristics of the gas and its abundance. For example, on a molecule-for-molecule basis methane is about eighty times stronger greenhouse gas than carbon dioxide, but it is present in much smaller concentrations so that its total contribution is smaller.
It is not possible to state that a certain gas causes an exact percentage of the greenhouse effect. This is because some of the gases absorb and emit radiation at the same frequencies as others, so that the total greenhouse effect is not simply the sum of the influence of each gas. The higher ends of the ranges quoted are for each gas alone; the lower ends account for overlaps with the other gases. The major non-gas contributor to the Earth's greenhouse effect, clouds, also absorb and emit infrared radiation and thus have an effect on radiative properties of the greenhouse gases.
In addition to the main greenhouse gases listed above, other greenhouse gases include sulfur hexafluoride, hydrofluorocarbons and perfluorocarbons (see IPCC list of greenhouse gases). Some greenhouse gases are not often listed. For example, nitrogen trifluoride has a high global warming potential (GWP) but is only present in very small quantities.
Scientists who have elaborated on Arrhenius' theory of global warming are concerned that increasing concentrations of greenhouse gases in the atmosphere are causing an unprecedented rise in global temperatures, with potentially harmful consequences for the environment and human health. Although contributing to many other physical and chemical reactions, the major atmospheric constituents, nitrogen (N2), oxygen (O2), and argon (Ar), are not greenhouse gases. This is because molecules containing two atoms of the same element such as N2 and O2 and monatomic molecules such as Ar have no net change in their dipole moment when they vibrate and hence are almost totally unaffected by infrared light. Although molecules containing two atoms of different elements such as carbon monoxide (CO) or hydrogen chloride (HCl) absorb IR, 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 and are not often included when discussing greenhouse gases.
Late 19th century scientists experimentally discovered that N2 and O2 do not absorb infrared radiation (called, at that time, "dark radiation") while, at the contrary, water, as true vapour or condensed in the form of microscopic droplets suspended in clouds, CO2 and other poly-atomic gaseous molecules do absorb infrared radiation. It was recognized in the early 20th century that the greenhouse gases in the atmosphere caused the Earth's overall temperature to be higher than it would be without them.
Natural and anthropogenic sources
Aside from purely human-produced synthetic halocarbons, most greenhouse gases have both natural and human-caused sources. During the pre-industrial Holocene, concentrations of existing gases were roughly constant. In the industrial era, human activities have added greenhouse gases to the atmosphere, mainly through the burning of fossil fuels and clearing of forests.
The 2007 Fourth Assessment Report compiled by the IPCC (AR4) noted that "changes in atmospheric concentrations of greenhouse gases and aerosols, land cover and solar radiation alter the energy balance of the climate system", and concluded that "increases in anthropogenic greenhouse gas concentrations is very likely to have caused most of the increases in global average temperatures since the mid-20th century". In AR4, "most of" is defined as more than 50%.
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. Direct data does not exist for periods earlier than those represented in the ice core record, a record which indicates CO2 mole fractions staying within a range of between 180ppm and 280ppm throughout the last 800,000 years, until the increase of the last 250 years. However, various proxies and modeling suggests larger variations in past epochs; 500 million years ago CO2 levels were likely 10 times higher than now. 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 Ma. 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 stabilising feedbacks. 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 Ma, by a colossal volcanic outgassing which raised the CO2 concentration of the atmosphere abruptly to 12%, about 350 times modern levels, causing extreme greenhouse conditions and carbonate deposition as limestone at the rate of about 1 mm per day. 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% of emissions from human sources.
Anthropogenic Greenhouse Gasses
Since about 1750 human activity has increased the concentration of carbon dioxide and other greenhouse gases. Measured atmospheric concentrations of carbon dioxide are currently 100 ppm higher than pre-industrial levels. 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, mainly photosynthesis of carbon compounds by plants and marine plankton. As a result of this balance, the atmospheric mole fraction 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.
It is likely that anthropogenic warming, such as that due to elevated greenhouse gas levels, has had a discernible influence on many physical and biological systems. Warming is projected to affect various issues such as freshwater resources, industry, food and health.
The main sources of greenhouse gases due to human activity are:
- burning of fossil fuels and deforestation leading to higher carbon dioxide concentrations in the air. Land use change (mainly deforestation in the tropics) account for up to one third of total anthropogenic CO2 emissions.
- livestock enteric fermentation and manure management, 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 (N2O) concentrations.
The US Environmental Protection Agency (EPA) ranks the major greenhouse gas contributing end-user sectors in the following order: industrial, transportation, residential, commercial and agricultural. Major sources of an individual's greenhouse gas include home heating and cooling, electricity consumption, and transportation. Corresponding conservation measures are improving home building insulation, installing geothermal heat pumps and 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.
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.
On December 7, 2009, the US Environmental Protection Agency released its final findings on greenhouse gases, declaring that "greenhouse gases (GHGs) threaten the public health and welfare of the American people". The finding applied to the same "six key well-mixed greenhouse gases" named in the Kyoto Protocol: carbon dioxide, methane, nitrous oxide, hydrofluorocarbons, perfluorocarbons, and sulfur hexafluoride.
Regional and National Attribution of Emissions
There are several different ways of measuring GHG emissions (see World Bank (2010, p. 362) for a table of national emissions data).
Some variables that have been reported include:
- Definition of measurement boundaries. Emissions can be attributed geographically, to the area where they were emitted (the territory principle) or by the activity principle to the territory that caused the emissions to be produced. These two principles would result in different totals when measuring for example the importation of electricity from one country to another or the emissions at an international airport.
- The time horizon of different GHGs. Contribution of a given GHG is reported as a CO2 equivalent; the calculation to determine this takes into account how long that gas remains in the atmosphere. This is not always known accurately and calculations must be regularly updated to take into account new information.
- What sectors are included in the calculation (e.g. energy industries, industrical processes, agriculture etc.). There is often a conflict between transparency and availability of data.
- The measurement protocol itself. This may be via direct measurement or estimation; the four main methods are the emission factor-based method, the mass balance method, the predictive emissions monitoring system and the continuing emissions monitoring systems. The methods differ in accuracy, but also in cost and usability.
The different measures are sometimes used by different countries in asserting various policy/ethical positions to do with climate change (Banuri et al., 1996, p. 94).[46] This use of different measures leads to a lack of comparability, which is problematic when monitoring progress towards targets. There are arguments for the adoption of a common measurement tool, or at least the development of communication between different tools.
Emissions may be measured over long time periods. This measurement type is called historical or cumulative emissions. Cumulative emissions give some indication of who is responsible for the build-up in the atmospheric concentration of GHGs (IEA, 2007, p. 199).
Emissions may also be measured across shorter time periods. Emissions changes may, for example, be measured against a base year of 1990. 1990 was used in the United Nations Framework Convention on Climate Change (UNFCCC) as the base year for emissions, and is also used in the Kyoto Protocol (some gases are also measured from the year 1995) (Grubb, 2003, pp. 146, 149). A country's emissions may also be reported as a proportion of global emissions for a particular year.
Another measurement is of per capita emissions. This divides a country's total annual emissions by its mid-year population (World Bank, 2010, p. 370). Per capita emissions may be based on historical or annual emissions (Banuri et al., 1996, pp. 106–107).
Cumulative emissions
Over the 1900-2005 period, the US was the world's largest cumulative emitter of energy-related CO2 emissions, and accounted for 30% of total cumulative emissions (IEA, 2007, p. 201). The second largest emitter was the EU, at 23%; the third largest was China, at 8%; fourth was Japan, at 4%; fifth was India, at 2%. The rest of the world accounted for 33% of global, cumulative, energy-related CO2 emissions.
Changes since a particular base year
In total, Annex I Parties managed a cut of 3.3% in GHG emissions between 1990 and 2004 (UNFCCC, 2007, p. 11). Annex I Parties are those countries listed in Annex I of the UNFCCC, and are the industrialized countries. For non-Annex I Parties, emissions in several large developing countries and fast growing economies (China, India, Thailand, Indonesia, Egypt, and Iran) GHG emissions have increased rapidly over this period (PBL, 2009).
The sharp acceleration in CO2 emissions since 2000 to more than a 3% increase per year (more than 2 ppm per year) from 1.1% per year during the 1990s is attributable to the lapse of formerly declining trends in carbon intensity of both developing and developed nations. China was responsible for most of global growth in emissions during this period. Localised 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. In comparison, methane has not increased appreciably, and N2O by 0.25% y−1
Annual and per capita emissions
At the present time, total annual emissions of GHGs are rising (Rogner et al., 2007). Between the period 1970 to 2004, emissions increased at an average rate of 1.6% per year, with CO2 emissions from the use of fossil fuels growing at a rate of 1.9% per year.
Today, the stock of carbon in the atmosphere increases by more than 3 million tonnes per annum (0.04%) compared with the existing stock. It seems less, but year after year is enormous cumulative. This increase is the result of human activities by burning fossil fuels, deforestation and forest degradation in tropical and boreal.
Per capita emissions in the industrialized countries are typically as much as ten times the average in developing countries (Grubb, 2003, p. 144). Due to China's fast economic development, its per capita emissions are quickly approaching the levels of those in the Annex I group of the Kyoto Protocol (PBL, 2009). Other countries with fast growing emissions are South Korea, Iran, and Australia. On the other hand, per capita emissions of the EU-15 and the USA are gradually decreasing over time. Emissions in Russia and the Ukraine have decreased fastest since 1990 due to economic restructuring in these countries (Carbon Trust, 2009, p. 24).
Energy statistics for fast growing economies are less accurate than those for the industrialized countries. For China's annual emissions in 2008, PBL (2008) estimated an uncertainty range of about 10%.
Removal from the atmosphere and global warming potential
Natural processes
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).
- a chemical reactions within the atmosphere. For example, methane is oxidized by reaction with naturally occurring hydroxyl radical, OH· and degraded to CO2 and water vapor (CO2 from the oxidation of methane is not included in the methane Global warming potential). Other chemical reactions include solution and solid phase chemistry occurring in atmospheric aerosols.
- a physical exchange between the atmosphere and the other compartments of the planet. An example is the mixing of atmospheric gases into the oceans.
- 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).
- 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).
Atmospheric lifetime
Aside from water vapor, which has a residence time of about nine days, major greenhouse gases are well-mixed, and take many years to leave the atmosphere. Although it is not easy to know with precision how long it takes greenhouse gases to leave the atmosphere, there are estimates for the principal greenhouse gases. Jacob (1999) defines the lifetime τ of an atmospheric species X in a one-box model as the average time that a molecule of X remains in the box. Mathematically τ can be defined as the ratio of the mass 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 (Fout), chemical loss of X (L), and deposition of X (D) (all in kg/sec): \tau = \frac{m}{F_{out}+L+D}
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.
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 gas has a high radiative forcing but also 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 the timescale considered.
Carbon dioxide has a variable atmospheric lifetime, and cannot be specified precisely.[64] 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. 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 72 over 20 years, 25 over 100 years and 7.6 over 500 years. The decrease in GWP at longer times is because methane is degraded to water and CO2 through chemical reactions in the atmosphere.
The use of CFC-12 (except some essential uses) has been phased out due to its ozone depleting properties. 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) 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.
Negative emissions
There exists a number of technologies which produce negative emissions of greenhouse gases. Most widely analysed are those which remove carbon dioxide from the atmosphere, either to geologic formations such as bio-energy with carbon capture and storage and carbon dioxide air capture, or to the soil as in the case with biochar. It has been pointed out by the IPCC, that many long-term climate scenario models require large scale manmade negative emissions in order to avoid serious climate change.
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 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) argue that the contribution to climate change from methane is at least double previous estimates as a result of this effect.
