Climate change indicators atmospheric concentrations of greenhouse gases climate change indicators in the united states us epa electricity and magnetism connect to form


• Concentrations of many of the halogenated gases shown in Figure 4 were essentially zero a few decades ago but have increased rapidly as they have chapter 7 electricity and magnetism been incorporated into industrial products and processes. Some of these chemicals have been or are currently being phased out of use because they are ozone-depleting substances, meaning they also cause harm to the Earth’s protective ozone layer. As a result, concentrations of many major ozone-depleting gases have begun to stabilize or decline (see Figure 4, left panel). Concentrations of other halogenated gases have continued to rise, however, especially where the gases have emerged as substitutes for ozone-depleting chemicals (see Figure 4, right panel).

• Overall, the total amount of ozone in the atmosphere decreased by about 3 percent between 1979 and 2014 (see Figure 5). All of the decrease happened in the stratosphere, with most of the decrease occurring between 1979 and 1994. Changes in stratospheric ozone reflect the effect of ozone-depleting substances. These chemicals have been released into the air for many years, but recently, international efforts have reduced emissions and phased out their use.

Since the Industrial Revolution began in the 1700s, people have added a substantial amount of greenhouse gases into the atmosphere by burning fossil fuels, cutting down forests, and electricity jeopardy powerpoint conducting other activities (see the U.S. and Global Greenhouse Gas Emissions indicators). When greenhouse gases are emitted into the atmosphere, many remain there for long time periods ranging from a decade to many millennia. Over time, these gases are removed from the atmosphere by chemical reactions or by emissions sinks, such as the oceans and vegetation, which absorb greenhouse gases from the atmosphere. As a result of human activities, however, these gases are entering the atmosphere more quickly than they are being removed, and thus their concentrations are increasing.

Carbon dioxide, methane, nitrous oxide, and certain manufactured gases called halogenated gases (gases that contain chlorine, fluorine, or bromine) become well mixed throughout the global atmosphere because of their relatively long lifetimes and because of transport by winds. Concentrations of these greenhouse gases are measured in parts per million (ppm), parts per billion (ppb gas 85 vs 87), or parts per trillion (ppt) by volume. In other words, a concentration of 1 ppb for a given gas means there is one molecule of that gas in every 1 billion molecules of air. Some halogenated gases are considered major greenhouse gases due to their very high global warming potentials and long atmospheric lifetimes even if they only exist at a few ppt ( see table).

This indicator includes several of the most important halogenated gases, but some others are not shown. Many other halogenated gases are also greenhouse gases, but Figure 4 is limited to a set of common examples that represent most of the major types of these gases. The indicator also does not address certain gas equations chemistry other pollutants that can affect climate by either reflecting or absorbing energy. For example, sulfate particles can reflect sunlight away from the Earth, while black carbon aerosols (soot) absorb energy. Data for nitrogen trifluoride (Figure 4) reflect modeled averages based on measurements made in the Northern Hemisphere and some locations in the Southern Hemisphere electricity storage cost per kwh, to represent global average concentrations over time. The global averages for ozone only cover the area between 50°N and 50°S latitude (77 percent of the Earth’s surface), because at higher latitudes the lack of sunlight in winter creates data gaps and the angle of incoming sunlight during the rest of the year reduces the accuracy of the satellite measuring technique.

9. Rigby, M. 2016 update to data originally published in: Arnold, T., C.M. Harth, J. Mühle, A.J. Manning, P.K. Salameh, J. Kim, D.J. Ivy, L.P. Steele, V.V. Petrenko, J.P. Severinghaus, D. Baggenstos, and R.F. Weiss. 2013. Nitrogen trifluoride global emissions estimated from updated atmospheric measurements. P. Natl. Acad. Sci. USA 110(6):2029–2034. Data updated July 2016.

14. IPCC (Intergovernmental Panel on Climate Change). 2013. Climate change 2013: The physical science basis. Working Group gas apple pay I contribution to the IPCC Fifth Assessment Report. Cambridge, United Kingdom: Cambridge University Press. Atmospheric Concentrations of Greenhouse Gases: Citations for Figures 1, 2, and 3 Figure 1

Etheridge, D.M., L.P. Steele, R.L. Langenfelds, R.J. Francey, J.-M. Barnola, and V.I. Morgan. 1998. Historical CO 2 records from the Law Dome DE08, DE08-2, and DSS ice cores. In: Trends: A compendium of data on global change. Oak Ridge, TN: U.S. Department of Energy. Accessed September 14, 2005.

Etheridge, D.M., L.P. Steele, R.J. Francey, and R.L. Langenfelds. 2002. Historic CH 4 records from Antarctic and Greenland ice cores, Antarctic firn data, and archived air samples from Cape Grim, Tasmania. In: Trends: A compendium of data on global change. Oak Ridge, TN: U.S. Department of Energy. Accessed September 13, 2005 electricity vs magnetism venn diagram.

Steele, L.P., P.B. Krummel, and R.L. Langenfelds. 2002. Atmospheric methane record from Shetland Islands, Scotland (October 2002 version). In: Trends: A compendium of data on global change. Oak Ridge, TN: U.S. Department of Energy. Accessed September 13, 2005. Figure 3

Schilt, A., M. Baumgartner, T. Blunier, J. Schwander, R. Spahni, H. Fischer, and T.F. Stocker. 2010. Glacial-interglacial and millennial scale variations in the atmospheric nitrous oxide concentration during the last 800,000 years. Quaternary Sci. Rev. 29:182–192.