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'Carbon dioxide in the Earth's atmosphere' is present in a low concentrations. Regardless, it is essential to photosynthesis in plants and other photoautotrophs, and is also a prominent greenhouse gas due to its radiative forcing strength.

Contents

Concentration

Origins

Historical variation

Relationship with oceanic concentration

See also

References

Concentration

As of January 2007, the CO₂ concentration in Earth's atmosphere was about 0.0383% by volume, or 383 ppmv. This is 99 ppm (38%) above the 1832 ice core levels of 284 ppm. The National Oceanic and Atmospheric Administration describes current levels "...as a dry mole fraction defined as the number of molecules of carbon dioxide divided by the number of molecules of dry air multiplied by one million (ppm)." and the chart as of July 2007 shows a level of about 387 ppm.^[1][2][3]
There is an annual fluctuation of about 3-9 ppm in the measurements, which roughly follows the Northern Hemisphere's growing season. The Northern Hemisphere dominates the annual cycle of CO₂ concentration because it has much greater land area and plant biomass than the Southern Hemisphere. Concentrations peak in May as the spring greenup begins and reach a minimum in October when the quantity of biomass undergoing photosynthesis is greatest.^[4]
Despite its relativly small concentration overall in the atmosphere, CO₂ is an important component of Earth's atmosphere because it absorbs infrared radiation at wavelengths of 4.26 µm (asymmetric stretching vibrational mode) and 14.99 µm (bending vibrational mode), thereby playing a role in the greenhouse effect.^[5] ''See also "Carbon dioxide equivalent"''.



The initial carbon dioxide in the atmosphere of the young Earth was produced by volcanic activity. This was essential for a warm and stable climate conducive to life. Volcanic activity now releases about 130 to 230 teragrams (145 million to 255 million short tons) of carbon dioxide each year,^[6] which is less than 1% of the amount released by human activities.^[7]

From 1832 to 2004, the atmospheric CO₂ concentration increased from 284 ppmv to 377 ppmv, or about 33%, with most of the change occurring since 1970. Burning fossil fuels such as coal and petroleum is the leading cause of increased man-made CO₂; deforestation is the second major cause. Around 24 billion tonnes of CO₂ are released from fossil fuels per year worldwide, equivalent to about 6 billion tonnes of carbon. (See List of countries by carbon dioxide emissions.)
Carbon dioxide is released to the atmosphere by a variety of natural sources, and over 95% percent of total emissions would occur even if humans were not present on Earth. For example, the natural decay of organic material in forests and grasslands, such as dead trees, results in the release of about 220 billion tons of carbon dioxide every year. These natural sources are balanced by natural sinks, which remove carbon dioxide from the atmosphere.^[8] The increase in carbon dioxide concentration arises because the increase from human activity is not balanced by a corresponding sink.

In 1997, Indonesian peat fires may have released 13% – 40% as much carbon as fossil fuel burning does in a single year.^[9][10] Various techniques have been proposed for removing excess carbon dioxide from the atmosphere in carbon dioxide sinks. Not all the emitted CO₂ remains in the atmosphere; some is absorbed in the oceans or biosphere. The ratio of the emitted CO₂ to the increase in atmospheric CO₂ is known as the ''airborne fraction'' (Keeling et al., 1995); this varies for short-term averages but is typically 57% over longer (5 year) periods.
Increased amounts of CO₂ in the atmosphere enhance the greenhouse effect. It is currently the majority scientific opinion that carbon dioxide emissions are the main cause of global warming observed since the latter half of the 20th century. The effect of combustion-produced carbon dioxide on climate is occasionally called the Callendar effect, after engineer and inventor Guy Stewart Callendar who was one of the first to propose this association.

Origins

Natural sources of atmospheric carbon dioxide include volcanic outgassing, the combustion of organic matter, and the respiration processes of living aerobic organisms; man-made sources of carbon dioxide come mainly from the burning of fossil fuels for heating, power generation and transport. It is also produced by various microorganisms from fermentation and cellular respiration. Plants convert carbon dioxide to carbohydrates during a process called photosynthesis. They produce the energy needed for this reaction through the photolysis of water. The resulting gas, oxygen, is released into the atmosphere by plants, which is subsequently used for respiration by heterotrophic organisms, forming a cycle.

Historical variation

The most direct method for measuring atmospheric carbon dioxide concentrations for periods before direct sampling is to measure bubbles of air (fluid or gas inclusions) trapped in the Antarctic or Greenland ice caps. The most widely accepted of such studies come from a variety of Antarctic cores and indicate that atmospheric CO₂ levels were about 260 – 280 ppmv immediately before industrial emissions began and did not vary much from this level during the preceding 10,000 years (10 kyr).
The longest ice core record comes from East Antarctica, where ice has been sampled to an age of 800 kyr BP (Before Present).^[11] During this time, the atmospheric carbon dioxide concentration has varied by volume between 180 – 210 ppm during ice ages, increasing to 280 – 300 ppm during warmer interglacials.^[12] The data can be accessed here.
Some studies have disputed the claim of stable CO₂ levels during the present interglacial of the last 10 kyr. Based on an analysis of fossil leaves, Wagner et al.^[13] argued that CO₂ levels during the period 7 – 10 kyr ago were significantly higher (~300 ppm) and contained substantial variations that may be correlated to climate variations. Others have disputed such claims, suggesting they are more likely to reflect calibration problems than actual changes in CO₂.^[14] Relevant to this dispute is the observation that Greenland ice cores often report higher and more variable CO₂ values than similar measurements in Antarctica. However, the groups responsible for such measurements (e.g., Smith et al.^[15]) believe the variations in Greenland cores result from ''in situ'' decomposition of calcium carbonate dust found in the ice. When dust levels in Greenland cores are low, as they nearly always are in
Antarctic cores, the researchers report good agreement between Antarctic and Greenland CO₂ measurements.

On longer timescales, various proxy measurements have been used to attempt to determine atmospheric carbon dioxide levels millions of years in the past. These include boron and carbon isotope ratios in certain types of marine sediments, and the number of stomata observed on fossil plant leaves. While these measurements give much less precise estimates of carbon dioxide concentration than ice cores, there is evidence for very high CO₂ volume concentrations between 200 and 150 myr BP of over 3,000 ppm and between 600 and 400 myr BP of over 6,000 ppm.^[16] On long timescales, atmospheric CO₂ content is determined by the balance among geochemical processes including organic carbon burial in sediments, silicate rock weathering, and vulcanism. The net effect of slight imbalances in the carbon cycle over tens to hundreds of millions of years has been to reduce atmospheric CO₂. The rates of these processes are extremely slow; hence they are of limited relevance to the atmospheric CO₂ response to emissions over the next hundred years. In more recent times, atmospheric CO₂ concentration continued to fall after about 60 myr BP, and there is geochemical evidence that volume concentrations were less than 300 ppm by about 20 myr BP. Low CO₂ concentrations may have been the stimulus that favored the evolution of C4 plants, which increased greatly in abundance between 7 and 5 myr BP. Present carbon dioxide levels are likely higher now than at any time during the past 20 myr^[17] and certainly higher than in the last few hundred thousand.

Relationship with oceanic concentration

The Earth's oceans contain a huge amount of carbon dioxide in the form of bicarbonate and carbonate ions — much more than the amount in the atmosphere. The bicarbonate is produced in reactions between rock, water, and carbon dioxide. One example is the dissolution of calcium carbonate:
:CaCO₃ + CO₂ + H₂O Ca²⁺ + 2 HCO₃^-
Reactions like this tend to buffer changes in atmospheric CO₂. However, since it produces an acidic compound, the pH of sea water is thought to go down with increasing carbon dioxide levels. Reactions between carbon dioxide and non-carbonate rocks also add bicarbonate to the seas, which can later undergo the reverse of the above reaction to form carbonate rocks, releasing half of the bicarbonate as CO₂. Over hundreds of millions of years this has produced huge quantities of carbonate rocks.
The vast majority of CO₂ added to the atmosphere will eventually be absorbed by the oceans and become bicarbonate ion, but the process takes on the order of a hundred years because most seawater rarely comes near the surface.
As the oceans warm, carbon dioxide solubility in the surface waters decreases markedly. However, the overall system is quite complex, as indicated above, and further details may be found in the article on the carbon solubility pump.
An unknown, though probably large, quantity of CO₂ is in the ocean sediments as a methane-carbon dioxide-water clathrates, one of the family of gas hydrates.

See also

★ Avoiding Dangerous Climate Change - A Scientific Symposium on Stabilisation of Greenhouse Gases

★ Greenhouse effect

★ Global warming

References

1.
2. http://cdiac.ornl.gov/ftp/trends/co2/maunaloa.co2
3. Trends in Atmospheric Carbon Dioxide - Mauna Loa
4. http://cdiac.ornl.gov/pns/faq.html
5. Petty, G.W.: ''A First Course in Atmospheric Radiation'', pages 229-251, Sundog Publishing, 2004
6. Gerlach, T.M., 1992, Present-day CO₂ emissions from volcanoes: Eos, Transactions, American Geophysical Union, Vol. 72, No. 23, June 4, 1991, pp. 249, and 254 – 255
7. U.S. Geological Survey, "Volcanic Gases and Their Effects" http://volcanoes.usgs.gov/Hazards/What/VolGas/volgas.html
8. US Global Change Research Information Office, "Common Questions about Climate Change" http://www.gcrio.org/ipcc/qa/05.html
9. http://www.ens-newswire.com/ens/nov2002/2002-11-08-06.asp
10. http://www.newscientist.com/article.ns?id=dn6613
11. http://news.bbc.co.uk/2/hi/science/nature/5314592.stm
12. http://pubs.acs.org/cen/news/83/i48/8348notw1.html
13.
14.
15. The CO₂ concentration of air trapped in GISP2 ice from the Last Glacial Maximum-Holocene transition, , H.J., Smith, Geophysical Research Letters, 1997
16. http://www.grida.no/climate/ipcc_tar/wg1/fig3-2.htm
17. http://www.grida.no/climate/ipcc_tar/wg1/107.htm#331