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Greenhouse gas

Heat-trapping gas in an atmosphere


Heat-trapping gas in an atmosphere

Greenhouse gases (GHGs) are the gases in an atmosphere that trap heat, raising the surface temperature of astronomical bodies such as Earth. Unlike other gases, greenhouse gases absorb the radiations that a planet emits, resulting in the greenhouse effect. The Earth is warmed by sunlight, causing its surface to radiate heat, which is then mostly absorbed by greenhouse gases. Without greenhouse gases in the atmosphere, the average temperature of Earth's surface would be about -18 °C, rather than the present average of 15 °C. Human-induced warming has been increasing at a rate that is unprecedented in the instrumental record, reaching 0.27 [0.2–0.4] °C per decade over 2015–2024. This high rate of warming is caused by a combination of greenhouse gas emissions being at an all-time high of 53.6±5.2 Gt CO2e yr−1 over the last decade (2014–2023), as well as reductions in the strength of aerosol cooling.

The five most abundant greenhouse gases in Earth's atmosphere, listed in decreasing order of average global mole fraction, are: water vapor, carbon dioxide, methane, nitrous oxide, ozone. Other greenhouse gases of concern include chlorofluorocarbons (CFCs and HCFCs), hydrofluorocarbons (HFCs), perfluorocarbons, , and . Water vapor causes about half of the greenhouse effect, acting in response to other gases as a climate change feedback.

Human activities since the beginning of the Industrial Revolution (around 1750) have increased carbon dioxide by over 50%, and methane levels by 150%. Carbon dioxide emissions are causing about three-quarters of global warming, while methane emissions cause most of the rest. The vast majority of carbon dioxide emissions by humans come from the burning of fossil fuels, with remaining contributions from agriculture and industry. Methane emissions originate from agriculture, fossil fuel production, waste, and other sources. The carbon cycle takes thousands of years to fully absorb from the atmosphere, while methane lasts in the atmosphere for an average of only 12 years.

Natural flows of carbon happen between the atmosphere, terrestrial ecosystems, the ocean, and sediments. These flows have been fairly balanced over the past one million years, although greenhouse gas levels have varied widely in the more distant past. Carbon dioxide levels are now higher than they have been for three million years. The 2023 annual update of key indicators reveals that human-induced temperature rise, greenhouse gas concentrations, and the Earth's energy imbalance have all reached new records. If current emission rates continue, then global warming will surpass 2.0 C-change sometime between 2040 and 2070. This is a level which the Intergovernmental Panel on Climate Change (IPCC) says is "dangerous".

Properties and mechanisms

Greenhouse gases are infrared active, meaning that they absorb and emit infrared radiation in the same long wavelength range as what is emitted by the Earth's surface, clouds and atmosphere.

99% of the Earth's dry atmosphere (excluding water vapor) is made up of nitrogen () (78%) and oxygen () (21%). Because their molecules contain two atoms of the same element, they have no asymmetry in the distribution of their electrical charges, and so are almost totally unaffected by infrared thermal radiation, with only an extremely minor effect from collision-induced absorption. A further 0.9% of the atmosphere is made up by argon (Ar), which is monatomic, and so completely transparent to thermal radiation. On the other hand, carbon dioxide (0.04%), methane, nitrous oxide and even less abundant trace gases account for less than 0.1% of Earth's atmosphere, but because their molecules contain atoms of different elements, there is an asymmetry in electric charge distribution which allows molecular vibrations to interact with electromagnetic radiation. This makes them infrared active, and so their presence causes greenhouse effect.

Radiative forcing

Main article: Radiative forcing

doi-access=free }} Figure 3.</ref>

Earth absorbs some of the radiant energy received from the sun, reflects some of it as light, and reflects or radiates the rest back to space as heat. A planet's surface temperature depends on this balance between incoming and outgoing energy. When Earth's energy balance is shifted, its surface becomes warmer or cooler, leading to a variety of changes in global climate. Radiative forcing is a metric calculated in watts per square meter, which characterizes the impact of an external change in a factor that influences climate. It is calculated as the difference in top-of-atmosphere (TOA) energy balance immediately caused by such an external change. A positive forcing, such as from increased concentrations of greenhouse gases, means more energy arriving than leaving at the top-of-atmosphere, which causes additional warming, while negative forcing, like from sulfates forming in the atmosphere from sulfur dioxide, leads to cooling.

Within the lower atmosphere, greenhouse gases exchange thermal radiation with the surface and limit radiative heat flow away from it, which reduces the overall rate of upward radiative heat transfer. The increased concentration of greenhouse gases is also cooling the upper atmosphere, as it is much thinner than the lower layers, and any heat re-emitted from greenhouse gases is more likely to travel further to space than to interact with the fewer gas molecules in the upper layers. The upper atmosphere is also shrinking as the result.

Chemical process contributions to radiative forcing

world map of carbon monoxide concentrations in the lower atmosphere
publisher=NASA }}</ref>

Some gases contribute indirectly to altering the TOA radiative balance through participation in chemical processes within the atmosphere.

Oxidation of CO to directly produces an unambiguous increase in radiative forcing although the reason is subtle. The peak of the thermal IR emission from Earth's surface is very close to a strong vibrational absorption band of (wavelength 15 microns, or wavenumber 667 cm−1). On the other hand, the single CO vibrational band only absorbs IR at much shorter wavelengths (4.7 microns, or 2145 cm−1), where the emission of radiant energy from Earth's surface is at least a factor of ten lower. Oxidation of methane to , which requires reactions with the OH radical, produces an instantaneous reduction in radiative absorption and emission since is a weaker greenhouse gas than methane. However, the oxidations of CO and are entwined since both consume OH radicals. In any case, the calculation of the total radiative effect includes both direct and indirect forcing.

A second type of indirect effect happens when chemical reactions in the atmosphere involving these gases change the concentrations of greenhouse gases. For example, the destruction of non-methane volatile organic compounds (NMVOCs) in the atmosphere can produce ozone. The size of the indirect effect can depend strongly on where and when the gas is emitted.

NMVOCs include a large variety of chemically different compounds, such as benzene, ethanol, formaldehyde, cyclohexane, 1,1,1-Trichloroethane and acetone. Essentially, NMVOCs are identical to volatile organic compounds (VOCs), but with methane excluded. Methane is excluded in air-pollution contexts because it is not toxic. It is however a very potent greenhouse gas, with low reactivity and thus a long lifetime in the atmosphere. An important subset of NMVOCs are the non-methane hydrocarbons (NMHCs). The same process that converts NMVOCs to carbon dioxide can also lead to the formation of tropospheric ozone. Halocarbons have an indirect effect because they destroy stratospheric ozone. Finally, hydrogen can lead to ozone production and increases as well as producing stratospheric water vapor. --

Contributions of specific gases to the greenhouse effect

Main article: 2223

This table shows the most important contributions to the overall greenhouse effect, without which the average temperature of Earth's surface would be about -18 °C, instead of around 15 °C. This table also specifies tropospheric ozone, because this gas has a cooling effect in the stratosphere, but a warming influence comparable to nitrous oxide and CFCs in the troposphere.

K&T (1997)Schmidt (2010)ContributorClear SkyWith CloudsClear SkyWith Clouds
Water vapor60416750
Clouds3125
26182419
Tropospheric ozone (O3)8
+6
Other997

Special role of water vapor

access-date=20 April 2014}}</ref>

Water vapor is the most important greenhouse gas overall, being responsible for 41–67% of the greenhouse effect, but its global concentrations are not directly affected by human activity. While local water vapor concentrations can be affected by developments such as irrigation, it has little impact on the global scale due to its short residence time of about nine days. Indirectly, an increase in global temperatures will also increase water vapor concentrations and thus their warming effect, in a process known as water vapor feedback. It occurs because the Clausius–Clapeyron relation holds that more water vapor will be present per unit volume at elevated temperatures. Thus, local atmospheric concentration of water vapor varies from less than 0.01% in extremely cold regions up to 3% by mass in saturated air at about 32 °C.

Global warming potential (GWP) and CO2 equivalents

List of all greenhouse gases

publisher=U.S. Global Change Research Program}}</ref>

The contribution of each gas to the enhanced greenhouse effect is determined by the characteristics of that gas, its abundance, and any indirect effects it may cause. For example, the direct radiative effect of a mass of methane is about 84 times stronger than the same mass of carbon dioxide over a 20-year time frame. Since the 1980s, greenhouse gas forcing contributions (relative to year 1750) are also estimated with high accuracy using IPCC-recommended expressions derived from radiative transfer models.

The concentration of a greenhouse gas is typically measured in parts per million (ppm) or parts per billion (ppb) by volume. A concentration of 420 ppm means that 420 out of every million air molecules is a molecule. The first 30 ppm increase in concentrations took place in about 200 years, from the start of the Industrial Revolution to 1958; however the next 90 ppm increase took place within 56 years, from 1958 to 2014. Similarly, the average annual increase in the 1960s was only 37% of what it was in 2000 through 2007.

Many observations are available online in a variety of Atmospheric Chemistry Observational Databases. The table below shows the most influential long-lived, well-mixed greenhouse gases, along with their tropospheric concentrations and direct radiative forcings, as identified by the Intergovernmental Panel on Climate Change (IPCC). Abundances of these trace gases are regularly measured by atmospheric scientists from samples collected throughout the world. It excludes water vapor because changes in its concentrations are calculated as a climate change feedback indirectly caused by changes in other greenhouse gases, as well as ozone, whose concentrations are only modified indirectly by various refrigerants that cause ozone depletion. Some short-lived gases (e.g. carbon monoxide, NOx) and aerosols (e.g. mineral dust or black carbon) are also excluded because of limited role and strong variation, along with minor refrigerants and other halogenated gases, which have been mass-produced in smaller quantities than those in the table. and Annex III of the 2021 IPCC WG1 Report

SpeciesLifetime100-yrMole Fraction [ppt – except as noted] + Radiative forcing [W m−2]ConcentrationsBaselineTARAR4AR5AR6
CO2 [ppm]1278365 **(1.46)**379 **(1.66)**391 **(1.82)**410 **(2.16)**[[File:Mauna_Loa_CO2_monthly_mean_concentration.svgupright=0.5frameless]]
CH4 [ppb]12.4287001,745 **(0.48)**1,774 **(0.48)**1,801 **(0.48)**1866 **(0.54)**[[File:CH4 mm.pngupright=0.5frameless]]
N2O [ppb]121265270314 **(0.15)**319 **(0.16)**324 **(0.17)**332 **(0.21)**[[File:HATS_Nitrous_Oxide_concentration.pngupright=0.5frameless]]
CFC-11454,6600268 **(0.07)**251 **(0.063)**238 **(0.062)**226 **(0.066)**[[File:Hats_f11_global.pngupright=0.5frameless]]
CFC-1210010,2000533 **(0.17)**538 **(0.17)**528 **(0.17)**503 **(0.18)**[[File:Hats_f12_global.pngupright=0.5frameless]]
CFC-1364013,90004 **(0.001)**2.7 **(0.0007)**3.28 **(0.0009)**[cfc13](https://agage2.eas.gatech.edu/data_archive/data_figures/monthly/pdf/CFC-13_mm.pdf)
[CFC-113](1-1-2-trichloro-1-2-2-trifluoroethane)856,490084 **(0.03)**79 **(0.024)**74 **(0.022)**70 **(0.021)**[[File:Hats_f113_global.pngupright=0.5frameless]]
[CFC-114](1-2-dichlorotetrafluoroethane)1907,710015 **(0.005)**16 **(0.005)**[cfc114](https://agage2.eas.gatech.edu/data_archive/data_figures/monthly/pdf/CFC-114_mm.pdf)
CFC-1151,0205,86007 **(0.001)**8.37 **(0.0017)**8.67 **(0.0021)**[cfc115](https://agage2.eas.gatech.edu/data_archive/data_figures/monthly/pdf/CFC-115_mm.pdf)
HCFC-2211.95,2800132 **(0.03)**169 **(0.033)**213 **(0.0447)**247 **(0.0528)**[[File:HCFC22_concentration.jpgupright=0.5frameless]]
HCFC-141b9.22,550010 **(0.001)**18 **(0.0025)**21.4 **(0.0034)**24.4 **(0.0039)**[[File:HCFC141b_concentration.jpgupright=0.5frameless]]
HCFC-142b17.25,020011 **(0.002)**15 **(0.0031)**21.2 **(0.0040)**22.3 **(0.0043)**[[File:HCFC142b_concentration.jpgupright=0.5frameless]]
[CH3CCl3](1-1-1-trichloroethane)5160069 **(0.004)**19 **(0.0011)**6.32 **(0.0004)**1.6 **(0.0001)**[[File:BK_MC.jpgupright=0.5frameless]]
CCl4261,7300102 **(0.01)**93 **(0.012)**85.8 **(0.0146)**78 **(0.0129)**[[File:Hats_ccl4_global.pngupright=0.5frameless]]
HFC-2322212,400014 **(0.002)**18 **(0.0033)**24 **(0.0043)**32.4 **(0.0062)**[[File:HFC-23_mm.pngupright=0.5frameless]]
HFC-325.267704.92 **(0.0005)**20 **(0.0022)**[[File:BK_HFC32.jpgupright=0.5frameless]]
HFC-12528.23,17003.7 **(0.0009)**9.58 **(0.0022)**29.4 **(0.0069)**[[File:HFC125_concentration.jpgupright=0.5frameless]]
HFC-134a13.41,30007.5 **(0.001)**35 **(0.0055)**62.7 **(0.0100)**107.6 **(0.018)**[[File:HFC-134a mm.pngupright=0.5frameless]]
HFC-143a47.14,800012.0 **(0.0019)**24 **(0.0040)**[[File:HFC143a_concentration.jpgupright=0.5frameless]]
HFC-152a1.513800.5 **(0.0000)**3.9 **(0.0004)**6.4 **(0.0006)**7.1 **(0.0007)**[[File:HFC152a_concentration.jpgupright=0.5frameless]]
CF4 (PFC-14)50,0006,6304080 **(0.003)**74 **(0.0034)**79 **(0.0040)**85.5 **(0.0051)**[[File:Tetrafluoromethane_concentration.jpgupright=0.5frameless]]
C2F6 (PFC-116)10,00011,1003 **(0.001)**2.9 **(0.0008)**4.16 **(0.0010)**4.85 **(0.0013)**[[File:Hexafluoroethane_concentration.jpgupright=0.5frameless]]
SF63,20023,5000.014.2 **(0.002)**5.6 **(0.0029)**7.28 **(0.0041)**9.95 **(0.0056)**[[File:Sulfur_Hexafluoride_concentration.pngupright=0.5frameless]]
SO2F2364,09001.71 **(0.0003)**2.5 **(0.0005)**[[File:SO2F2_mm.pngupright=0.5frameless]]
NF350016,10000.9 **(0.0002)**2.05 **(0.0004)**[[File:Nitrogen_Trifluoride_concentration.jpgupright=0.5frameless]]

Factors affecting concentrations

Atmospheric concentrations are determined by the balance between sources (emissions of the gas from human activities and natural systems) and sinks (the removal of the gas from the atmosphere by conversion to a different chemical compound or absorption by bodies of water).

Airborne fraction

The proportion of an emission remaining in the atmosphere after a specified time is the "airborne fraction" (AF). The annual airborne fraction is the ratio of the atmospheric increase in a given year to that year's total emissions. The annual airborne fraction for had been stable at 0.45 for the past six decades even as the emissions have been increasing. This means that the other 0.55 of emitted is absorbed by the land and atmosphere carbon sinks within the first year of an emission. In the high-emission scenarios, the effectiveness of carbon sinks will be lower, increasing the atmospheric fraction of even though the raw amount of emissions absorbed will be higher than in the present.

Atmospheric lifetime

Estimated atmospheric methane lifetime before the industrial era (shaded area); changes in methane lifetime since 1850 as simulated by a climate model (blue line), and the reconciled graph (red line).<ref name=&quot;Arora2018&quot; />

Major greenhouse gases are well mixed and take many years to leave the atmosphere.

The atmospheric lifetime of a greenhouse gas refers to the time required to restore equilibrium following a sudden increase or decrease 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. This can be represented through the following formula, where the lifetime \tau of an atmospheric species X in a one-box model is the average time that a molecule of X remains in the box.

\tau can also 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 (F_\text{out}), chemical loss of X (L), and deposition of X (D) (all in kg/s): :\tau = \frac{m}{F_\text{out}+L+D}. If input of this gas into the box ceased, then after time \tau, its concentration would decrease by about 63%.

Changes to any of these variables can alter the atmospheric lifetime of a greenhouse gas. For instance, methane's atmospheric lifetime is estimated to have been lower in the 19th century than now, but to have been higher in the second half of the 20th century than after 2000. Carbon dioxide has an even more variable lifetime, which cannot be specified down to a single number. Scientists instead say that while the first 10% of carbon dioxide's airborne fraction (not counting the ~50% absorbed by land and ocean sinks within the emission's first year) is removed "quickly", the vast majority of the airborne fraction – 80% – lasts for "centuries to millennia". The remaining 10% stays for tens of thousands of years. In some models, this longest-lasting fraction is as large as 30%.{{cite web |date=17 January 2023 |title=How long will global warming last? |url= https://climate.mit.edu/ask-mit/how-do-we-know-how-long-carbon-dioxide-remains-atmosphere |publisher=MIT Climate Portal }}

A comparison of CO2 persistence in the atmosphere with an exponential decay function with the same half-life

During geologic time scales

Monitoring

Greenhouse gas monitoring involves the direct measurement of atmospheric concentrations and direct and indirect measurement of greenhouse gas emissions. Indirect methods calculate emissions of greenhouse gases based on related metrics such as fossil fuel extraction.

There are several different methods of measuring carbon dioxide concentrations in the atmosphere, including infrared analyzing and manometry. Methane and nitrous oxide are measured by other instruments, such as the range-resolved infrared differential absorption lidar (DIAL). Greenhouse gases are measured from space such as by the Orbiting Carbon Observatory and through networks of ground stations such as the Integrated Carbon Observation System.

The Annual Greenhouse Gas Index (AGGI) is defined by atmospheric scientists at NOAA as the ratio of total direct radiative forcing due to long-lived and well-mixed greenhouse gases for any year for which adequate global measurements exist, to that present in year 1990. These radiative forcing levels are relative to those present in year 1750 (i.e. prior to the start of the industrial era). 1990 is chosen because it is the baseline year for the Kyoto Protocol, and is the publication year of the first IPCC Scientific Assessment of Climate Change. As such, NOAA states that the AGGI "measures the commitment that (global) society has already made to living in a changing climate. It is based on the highest quality atmospheric observations from sites around the world. Its uncertainty is very low."

Data networks

Types of sources

Natural sources

The natural flows of carbon between the atmosphere, ocean, terrestrial ecosystems, and sediments are fairly balanced; so carbon levels would be roughly stable without human influence. Carbon dioxide is removed from the atmosphere primarily through photosynthesis and enters the terrestrial and oceanic biospheres. Carbon dioxide also dissolves directly from the atmosphere into bodies of water (ocean, lakes, etc.), as well as dissolving in precipitation as raindrops fall through the atmosphere. When dissolved in water, carbon dioxide reacts with water molecules and forms carbonic acid, which contributes to ocean acidity. It can then be absorbed by rocks through weathering. It also can acidify other surfaces it touches or be washed into the ocean.

Human-made sources

Taking into account direct and indirect emissions, industry is the sector with the highest share of global emissions. Data as of 2019 from the IPCC.

Main article: Greenhouse gas emissions

The vast majority of carbon dioxide emissions by humans come from the burning of fossil fuels. Additional contributions come from cement manufacturing, fertilizer production, and changes in land use like deforestation. Methane emissions originate from agriculture, fossil fuel production, waste, and other sources. Rice paddies are a significant agricultural source of greenhouse gas emissions, contributing 22% of total agricultural methane and 11% of nitrous oxide emissions.

If current emission rates continue then temperature rises will surpass 2.0 C-change sometime between 2040 and 2070, which is the level the United Nations' Intergovernmental Panel on Climate Change (IPCC) says is "dangerous".

Most greenhouse gases have both natural and human-caused sources. An exception are purely human-produced synthetic halocarbons which have no natural sources. During the pre-industrial Holocene, concentrations of existing gases were roughly constant, because the large natural sources and sinks roughly balanced. In the industrial era, human activities have added greenhouse gases to the atmosphere, mainly through the burning of fossil fuels and clearing of forests.

Reducing human-caused greenhouse gases

Main article: Climate change mitigation

Needed emissions cuts

Removal from the atmosphere through negative emissions

Main article: Carbon dioxide removal, Net-zero emissions, Carbon sink

Several technologies remove greenhouse gas emissions from the atmosphere. Most widely analyzed are those that 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. Many long-term climate scenario models require large-scale human-made negative emissions to avoid serious climate change.

Negative emissions approaches are also being studied for atmospheric methane, called atmospheric methane removal.

History of discovery

In the late 19th century, scientists experimentally discovered that and do not absorb infrared radiation (called, at that time, "dark radiation"), while water (both as true vapor and condensed in the form of microscopic droplets suspended in clouds) and and other poly-atomic gaseous molecules do absorb infrared radiation. In the early 20th century, researchers realized that greenhouse gases in the atmosphere made Earth's overall temperature higher than it would be without them. The term greenhouse was first applied to this phenomenon by Nils Gustaf Ekholm in 1901.

During the late 20th century, a scientific consensus evolved that increasing concentrations of greenhouse gases in the atmosphere cause a substantial rise in global temperatures and changes to other parts of the climate system, with consequences for the environment and for human health.

Other planets

Greenhouse gases exist in many atmospheres, creating greenhouse effects on Mars, Titan, and particularly in the thick atmosphere of Venus. While Venus has been described as the ultimate end state of runaway greenhouse effect, such a process would have virtually no chance of occurring from any increases in greenhouse gas concentrations caused by humans, as the Sun's brightness is too low and it would likely need to increase by some tens of percents, which will take a few billion years.

References

References

  1. (2021-08-09). "Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change". [[IPCC]] / [[Cambridge University Press]].
  2. Le Treut, H., R. Somerville, U. Cubasch, Y. Ding, C. Mauritzen, A. Mokssit, T. Peterson and M. Prather, 2007: "[https://www.ipcc.ch/site/assets/uploads/2018/03/ar4-wg1-chapter1.pdf Chapter 1: Historical Overview of Climate Change]". In: "[https://www.ipcc.ch/report/ar4/wg1/ Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change]". [Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M. Tignor and H.L. Miller (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA.
  3. (2025). "Indicators of Global Climate Change 2024: annual update of key indicators of the state of the climate system and human influence". Journal Earth System Science Data.
  4. (2016-08-01). "Atmospheric Concentration of Greenhouse Gases". [[U.S. Environmental Protection Agency]].
  5. . (). ["Inside the Earth's invisible blanket."](http://sequestration.org/science/greenhousegases.html). **.
  6. Gavin Schmidt. (2010-10-01). "Taking the Measure of the Greenhouse Effect". NASA Goddard Institute for Space Studies – Science Briefs.
  7. (3 June 2022). "Carbon dioxide now more than 50% higher than pre-industrial levels". National Oceanic and Atmospheric Administration.
  8. "Understanding methane emissions". International Energy Agency.
  9. (12 January 2016). "Global Greenhouse Gas Emissions Data". United States Environmental Protection Agency.
  10. (12 January 2016). "Global Greenhouse Gas Emissions Data". [[United States Environmental Protection Agency.
  11. Canadell, J.G., P.M.S. Monteiro, M.H. Costa, L. Cotrim da Cunha, P.M. Cox, A.V. Eliseev, S. Henson, M. Ishii, S. Jaccard, C. Koven, A. Lohila, P.K. Patra, S. Piao, J. Rogelj, S. Syampungani, S. Zaehle, and K. Zickfeld, 2021: [https://www.ipcc.ch/report/ar6/wg1/downloads/report/IPCC_AR6_WGI_Chapter05.pdf Chapter 5: Global Carbon and other Biogeochemical Cycles and Feedbacks]. In [https://www.ipcc.ch/report/ar6/wg1/ Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change] [Masson-Delmotte, V., P. Zhai, A. Pirani, S.L. Connors, C. Péan, S. Berger, N. Caud, Y. Chen, L. Goldfarb, M.I. Gomis, M. Huang, K. Leitzell, E. Lonnoy, J.B.R. Matthews, T.K. Maycock, T. Waterfield, O. Yelekçi, R. Yu, and B. Zhou (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, pp. 673–816, doi:10.1017/9781009157896.007.
  12. (21 February 2023). "Global Methane Tracker 2023". International Energy Agency.
  13. (16 December 2015). "Climate Change Indicators: Greenhouse Gases". United States Environmental Protection Agency.
  14. "Understanding methane emissions". International Energy Agency.
  15. (27 June 2016). "Climate Change Indicators: Atmospheric Concentrations of Greenhouse Gases". U.S. Environmental Protection Agency.
  16. "Climate Change: Atmospheric Carbon Dioxide".
  17. (2024-06-05). "Indicators of Global Climate Change 2023: annual update of key indicators of the state of the climate system and human influence". Earth System Science Data.
  18. (2020-12-04). "Analysis: When might the world exceed 1.5C and 2C of global warming?".
  19. IPCC, 2021: [https://www.ipcc.ch/report/ar6/wg1/downloads/report/IPCC_AR6_WGI_AnnexVII.pdf Annex VII: Glossary] [Matthews, J.B.R., V. Möller, R. van Diemen, J.S. Fuglestvedt, V. Masson-Delmotte, C.  Méndez, S. Semenov, A. Reisinger (eds.)]. In [https://www.ipcc.ch/report/ar6/wg1/ Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change] [Masson-Delmotte, V., P. Zhai, A. Pirani, S.L. Connors, C. Péan, S. Berger, N. Caud, Y. Chen, L. Goldfarb, M.I. Gomis, M. Huang, K. Leitzell, E. Lonnoy, J.B.R. Matthews, T.K. Maycock, T. Waterfield, O. Yelekçi, R. Yu, and B. Zhou (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA, pp. 2215–2256, [[doi:10.1017/9781009157896.022]].
  20. (6 October 2018). "Absorption coefficient of carbon dioxide across atmospheric troposphere layer". [[Heliyon]].
  21. (24 May 2012). "The natural greenhouse effect of atmospheric oxygen (O2) and nitrogen (N2)". Geophysical Research Letters.
  22. "Which Gases Are Greenhouse Gases?". American Chemical Society.
  23. (24 May 2012). "The natural greenhouse effect of atmospheric oxygen (O2) and nitrogen (N2)". Geophysical Research Letters.
  24. (2011). "Global Warming: Understanding the Forecast, Chapter 4: Greenhouse Gases". Wiley.
  25. (3 February 2025). "Global Warming Has Accelerated: Are the United Nations and the Public Well-Informed?". Environment.
  26. (2016). "Climate Change Indicators in the United States – Greenhouse Gases". U.S. Environmental Protection Agency (EPA).
  27. (2016). "Climate Change Indicators in the United States – Climate Forcing". U.S. Environmental Protection Agency (EPA).
  28. (2006). "Atmospheric Science". Academic Press.
  29. (1964). "Thermal Equilibrium of the Atmosphere with a Convective Adjustment". J. Atmos. Sci..
  30. Hatfield, Miles. (30 June 2021). "NASA Satellites See Upper Atmosphere Cooling and Contracting Due to Climate Change". [[NASA]].
  31. (2010). "Principles of Planetary Climate". Cambridge University Press.
  32. "The Chemistry of Earth's Atmosphere". NASA.
  33. Forster, P.. (2007). "Changes in Atmospheric Constituents and in Radiative Forcing". Cambridge University Press.
  34. (2014). "Section 2: Meteorology and Air Pollutants". John Wiley & Sons, Ltd.
  35. "System of Registries". US EPA.
  36. (2007). "Volatile Organic Compounds in the Atmosphere". Blackwell Publishing Ltd.
  37. (8 April 2022). "Hydrogen 'twice as powerful a greenhouse gas as previously thought': UK government study".
  38. (March 1998). "Science Briefs: Greenhouse Gases: Refining the Role of Carbon Dioxide".
  39. (2003). "Modern global climate change". Science.
  40. (2016-08-01). "Atmospheric Concentration of Greenhouse Gases". [[U.S. Environmental Protection Agency]].
  41. Kiehl, J.T.. (1997). "Earth's annual global mean energy budget". Bulletin of the American Meteorological Society.
  42. (4 June 2012). "The attribution of the present-day total greenhouse effect". J. Geophys. Res..
  43. (January 14, 2009). "NASA: Climate Forcings and Global Warming".
  44. (27 April 1995). "AGU Water Vapor in the Climate System". Eso.org.
  45. (November 2000). "Water vapor feedback and global warming". [[Annual Review of Energy and the Environment]].
  46. Evans, Kimberly Masters. (2005). "The environment: a revolution in attitudes". Thomson Gale.
  47. (2026). "The NOAA Annual Greenhouse Gas Index (AGGI)". National Oceanic and Atmospheric Administration (NOAA).
  48. "Annual Greenhouse Gas Index". U.S. Global Change Research Program.
  49. "Intergovernmental Panel on Climate Change Fifth Assessment Report".
  50. Butler J. and Montzka S.. (2020). "The NOAA Annual Greenhouse Gas Index (AGGI)". [[NOAA]] Global Monitoring Laboratory/Earth System Research Laboratories.
  51. Charles J. Kibert. (2016). "Sustainable Construction: Green Building Design and Delivery". Wiley.
  52. (2005). "Full Mauna Loa CO2 record". Earth System Research Laboratories.
  53. Tans, Pieter. (3 May 2008). ["Annual CO2 mole fraction increase (ppm) for 1959–2007"](ftp://ftp.cmdl.noaa.gov/ccg/co2/trends/co2_gr_mlo.txt }} {{cite web). J. Geophys. Res..
  54. "AR5 Climate Change 2013: The Physical Science Basis".
  55. "Global Monitoring Laboratory". NOAA Earth System Research Laboratories.
  56. "World Data Centre for Greenhouse Gases". World Meteorological Organization Global Atmosphere Watch Programme and Japan Meteorological Agency.
  57. "Advanced Global Atmospheric Gas Experiment". Massachusetts Institute of Technology.
  58. (2021-08-09). "Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change". Cambridge University Press.
  59. Hansen, J.. (2005). "Efficacy of Climate Forcings". Journal of Geophysical Research: Atmospheres.
  60. "Long-term global trends of atmospheric trace gases". NOAA Earth System Research Laboratories.
  61. "AGAGE Data and Figures". Massachusetts Institute of Technology.
  62. "TAR Climate Change 2001: The Scientific Basis".
  63. "AR4 Climate Change 2007: The Physical Science Basis".
  64. "Intergovernmental Panel on Climate Change Fifth Assessment Report – Supplemental Material".
  65. Archer, David. (2009). "Atmospheric lifetime of fossil fuel carbon dioxide". Annual Review of Earth and Planetary Sciences.
  66. Joos, F.. (2013). "Carbon dioxide and climate impulse response functions for the computation of greenhouse gas metrics: A multi-model analysis". Atmospheric Chemistry and Physics.
  67. Gribble, Gordon W.. (2009). "Naturally Occurring Organohalogen Compounds – A Comprehensive Update". Springer Science and Business Media.
  68. (1998). "Natural CF4 and SF6 on Earth". Geophysical Research Letters.
  69. Denman, K.L., G. Brasseur, A. Chidthaisong, P. Ciais, P.M. Cox, R.E. Dickinson, D. Hauglustaine, C. Heinze, E. Holland, D. Jacob, U. Lohmann, S Ramachandran, P.L. da Silva Dias, S.C. Wofsy and X. Zhang, 2007: [https://www.ipcc.ch/site/assets/uploads/2018/02/ar4-wg1-chapter7-1.pdf Chapter 7: Couplings Between Changes in the Climate System and Biogeochemistry]. In: [https://www.ipcc.ch/report/ar4/wg1/ Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change] [Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M.Tignor and H.L. Miller (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA.
  70. (2020). "Global Carbon Budget 2020". Earth System Science Data.
  71. (2021). "IPCC Sixth Assessment Report: Working Group 1".
  72. Betts. (2001). "Chapter 6 Radiative Forcing of Climate Change". UNEP/GRID-Arendal – Publications.
  73. Jacob, Daniel. (1999). "Introduction to atmospheric chemistry". [[Princeton University Press]].
  74. Eshelman, Anna. "Greenhouse Gases and Global Warming".
  75. (1 August 2018). "An assessment of natural methane fluxes simulated by the CLASS-CTEM model". Biogeosciences.
  76. (15 March 2005). "How long will global warming last?". RealClimate.
  77. Atkinson, Kate. (19 July 2023). "How long will global warming last?". [[Australian Associated Press]].
  78. Harris, Daniel C.. (2010). "Charles David Keeling and the Story of Atmospheric CO2 Measurements". Analytical Chemistry.
  79. (2017). "Differential Absorption Lidar (DIAL) Measurements of Landfill Methane Emissions". Remote Sensing.
  80. Butler J. and Montzka S.. (2020). "The NOAA Annual Greenhouse Gas Index (AGGI)". [[NOAA]] Global Monitoring Laboratory/Earth System Research Laboratories.
  81. LuAnn Dahlman. (14 August 2020). "Climate change: annual greenhouse gas index". NOAA Climate.gov science news & Information for a climate smart nation.
  82. "The NOAA Annual Greenhouse Gas Index (AGGI) – An Introduction". [[NOAA]] Global Monitoring Laboratory/Earth System Research Laboratories.
  83. Prentice, I.C.. (2001). "Climate change 2001: the scientific basis: contribution of Working Group I to the Third Assessment Report of the Intergouvernmental Panel on Climate Change".
  84. (2009). "An Introduction to the Global Carbon Cycle". University of New Hampshire.
  85. "Many Planets, One Earth // Section 4: Carbon Cycling and Earth's Climate". Many Planets, One Earth.
  86. "AR4 SYR Synthesis Report Summary for Policymakers – 2 Causes of change". ipcc.ch.
  87. (October 2023). "Greenhouse gas emissions and mitigation in rice agriculture". Nature Reviews Earth & Environment.
  88. (2000). "Chapter 3, IPCC Special Report on Emissions Scenarios, 2000". Intergovernmental Panel on Climate Change.
  89. (2009). "Geoengineering the climate: science, governance and uncertainty". The Royal Society.
  90. Fisher, B.S., N. Nakicenovic, K. Alfsen, J. Corfee Morlot, F. de la Chesnaye, J.-Ch. Hourcade, K. Jiang, M. Kainuma, E. La Rovere, A. Matysek, A. Rana, K. Riahi, R. Richels, S. Rose, D. van Vuuren, R. Warren, 2007: [https://www.ipcc.ch/site/assets/uploads/2018/02/ar4-wg3-chapter3-1.pdf Chapter 3: Issues related to mitigation in the long term context], In [https://www.ipcc.ch/report/ar4/wg3/ Climate Change 2007: Mitigation. Contribution of Working Group III to the Fourth Assessment Report of the Inter-governmental Panel on Climate Change] [B. Metz, O.R. Davidson, P.R. Bosch, R. Dave, L.A. Meyer (eds)], Cambridge University Press, Cambridge,
  91. (2021-11-15). "Atmospheric methane removal: a research agenda". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
  92. (14 August 1912). "Coal Consumption Affecting Climate". Rodney and Otamatea Times, Waitemata and Kaipara Gazette.
  93. (1896). "On the influence of carbonic acid in the air upon the temperature of the ground". The London, Edinburgh, and Dublin Philosophical Magazine and Journal of Science.
  94. (1897). "On the Influence of Carbonic Acid in the Air Upon the Temperature of the Ground". Publications of the Astronomical Society of the Pacific.
  95. (18 August 2015). "Who first coined the term "Greenhouse Effect"?".
  96. Ekholm N. (1901). "On The Variations Of The Climate Of The Geological And Historical Past And Their Causes". Quarterly Journal of the Royal Meteorological Society.
  97. (2013). "Quantifying the consensus on anthropogenic global warming in the scientific literature". Environmental Research Letters.
  98. Eddie Schwieterman. "Comparing the Greenhouse Effect on Earth, Mars, Venus, and Titan: Present Day and through Time".
  99. "Scoping of the IPCC 5th Assessment Report Cross Cutting Issues". Thirty-first Session of the IPCC Bali, 26–29 October 2009.
  100. (2013). "Climate sensitivity, sea level and atmospheric carbon dioxide". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
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