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== Executive Summary == <div id="h1-1-siblings" class="h1-siblings"></div> It is unequivocal that the increases in atmospheric carbon dioxide (CO <sub>2</sub> ), methane (CH <sub>4</sub> ) and nitrous oxide (N <sub>2</sub> O) since the pre-industrial period are caused by human activities. The accumulation of GHGs in the atmosphere is determined by the balance between anthropogenic emissions, anthropogenic removals, and physical-biogeochemical source and sink dynamics on land and in the ocean. This chapter assesses how physical and biogeochemical processes of the carbon and nitrogen cycles affect the variability and trends of GHGs in the atmosphere as well as ocean acidification and deoxygenation. It identifies physical and biogeochemical feedbacks that have affected (or could affect) future rates of GHG accumulation in the atmosphere, and therefore, influence climate change and its impacts. This chapter also assesses the remaining carbon budget to limit global warming within various goals, as well as the large-scale consequences of carbon dioxide removal (CDR) and solar radiation modification (SRM) on biogeochemical cycles. {Figures 5.1, 5.2} . <div id="The" class="h2-container"></div> <span id="the-human-perturbation-of-the-carbon-and-biogeochemical-cycles"></span> === The Human Perturbation of the Carbon and Biogeochemical Cycles === <div id="h2-1-siblings" class="h2-siblings"></div> '''Global mean concentrations for well-mixed GHGs (CO''' <sub>2</sub> ''', CH''' <sub>4</sub> '''and N''' <sub>2</sub> '''O) in 2019 correspond to increases of about 47%, 156%, and 23%, respectively, above the levels in 1750 (representative of the pre-industrial era)''' ( ''high confidence'' ''').''' Current atmospheric concentrations of the three GHGs are higher than at any point in the last 800,000 years, and in 2019 reached 409.9 parts per million (ppm) of CO <sub>2</sub> , 1866.3 parts per billion (ppb) of CH <sub>4</sub> , and 332.1 ppb of N <sub>2</sub> O ( ''very'' ''high confidence'' ). Current CO <sub>2</sub> concentrations in the atmosphere are also unprecedented in the last 2 million years ( ''high confidence'' ). In the past 60 million years, there have been periods in Earth’s history when CO <sub>2</sub> concentrations were significantly higher than at present, but multiple lines of evidence show that the rate at which CO <sub>2</sub> has increased in the atmosphere during 1900–2019 is at least 10 times faster than at any other time during the last 800,000 years ( ''high confidence'' ), and 4–5 times faster than during the last 56 million years ( ''low confidence'' ). {5.1.1, 2.2.3; Figures 5.3, 5.4; Cross-Chapter Box 2.1} <div id="Contemporary" class="h2-container"></div> <span id="contemporary-trends-of-greenhouse-gases"></span> === Contemporary Trends of Greenhouse Gases === <div id="h2-2-siblings" class="h2-siblings"></div> '''It is unequivocal that the increase of CO''' <sub>2</sub> ''', CH''' <sub>4</sub> ''', and N''' <sub>2</sub> '''O in the atmosphere over the industrial era is the result of human activities''' ( ''very high confidence'' ''').''' This assessment is based on multiple lines of evidence including atmospheric gradients, isotopes, and inventory data. During the last measured decade, global average annual anthropogenic emissions of CO <sub>2</sub> , CH <sub>4</sub> , and N <sub>2</sub> O, reached the highest levels in human history at 10.9 ± 0.9 petagrams of carbon per year (PgC yr <sup>–1</sup> , 2010–2019), 335–383 teragrams of methane per year (TgCH <sub>4</sub> yr <sup>–1</sup> , 2008–2017), and 4.2–11.4 teragrams of nitrogen per year (TgN yr <sup>–1</sup> , 2007–2016), respectively ( ''high confidence'' ). {5.2.1, 5.2.2, 5.2.3, 5.2.4; Figures 5.6, 5.13, 5.15} . '''The CO''' <sub>2</sub> '''emitted from human activities during the decade of 2010–2019 (decadal average 10.9 ± 0.9''' '''PgC y''' '''r''' –1 ''') was distributed between three Earth system components: 46% accumulated in the atmosphere (5.1 ± 0.02''' '''PgC y''' '''r''' –1 '''), 23% was taken up by the ocean (2.5 ± 0.6''' '''PgC y''' '''r''' –1 ''') and 31% was stored by vegetation in terrestrial ecosystems (3.4 ± 0.9''' '''PgC y''' '''r''' –1 ''')''' ( ''high confidence'' ''').''' Of the total anthropogenic CO <sub>2</sub> emissions, the combustion of fossil fuels was responsible for 81–91%, with the remainder being the net CO <sub>2</sub> flux from land-use change and land management (e.g., deforestation, degradation, regrowth after agricultural abandonment, and peat drainage). {5.2.1.2, 5.2.1.5; Table 5.1; Figures 5.5, 5.7, 5.12} '''Over the past six decades, the average fraction of anthropogenic CO''' <sub>2</sub> '''emissions that has accumulated in the atmosphere (referred to as the airborne fraction) has remained nearly constant at approximately 44%.''' The ocean and land sinks of CO <sub>2</sub> have continued to grow over the past six decades in response to increasing anthropogenic CO <sub>2</sub> emissions ( ''high confidence)'' . Interannual and decadal variability of the regional and global ocean and land sinks indicate that these sinks are sensitive to climate conditions and therefore to climate change ( ''high confidence'' ). {5.2.1.1, 5.2.1.2, 5.2.1.3, 5.2.1.4; Figures 5.7, 5.8, 5.10} '''Recent observations show that ocean carbon processes are starting to change in response to the growing ocean sink, and these changes are expected to contribute significantly to future weakening of the ocean sink under medium- to high-emissions scenarios.''' However, the effects of these changes are not yet reflected in a weakening trend of the contemporary (1960–2019) ocean sink ( ''high confidence'' ). {5.1.2, 5.2.1.3, 5.3.2.1; Figures 5.8, 5.20; Cross-Chapter Box 5.3} '''Atmospheric concentration of CH''' <sub>4</sub> '''grew at an average rate of 7.6 ± 2.7 ppb y''' '''r''' –1 '''for the last decade (2010–2019), with a faster growth of 9.3 ± 2.4 ppb y''' '''r''' –1 '''over the last six years (2014–2019)''' ( ''high confidence'' ''').''' The multi-decadal growth trend in atmospheric CH <sub>4</sub> is dominated by anthropogenic activities ( ''high confidence'' ), and the growth since 2007 is largely driven by emissions from both fossil fuels and agriculture (dominated by livestock) ( ''medium confidence)'' . The interannual variability is dominated by El Niño–Southern Oscillation cycles, during which biomass burning and wetland emissions, as well as loss by reaction with tropospheric hydroxyl radical (OH) play an important role. {5.2.2; Figures 5.13, 5.14; Table 5.2; Cross-Chapter Box 5.2} '''Atmospheric concentration of N''' <sub>2</sub> '''O grew at an average rate of 0.85 ± 0.03 ppb y''' '''r''' –1 '''between 1995 and 2019, with a further increase to 0.95 ± 0.04 ppb y''' '''r''' –1 '''in the most recent decade (2010–2019).''' This increase is dominated by anthropogenic emissions, which have increased by 30% between the 1980s and the most recent observational decade (2007–2016) ( ''high confidence'' ). Increased use of nitrogen fertilizer and manure contributed to about two-thirds of the increase during the 1980–2016 period, with the fossil fuels/industry, biomass burning, and wastewater accounting for much of the rest ( ''high confidence'' ). {5.2.3; Figures 5.15, 5.16, 5.17} <div id="Ocean" class="h2-container"></div> <span id="ocean-acidification-and-ocean-deoxygenation"></span> === Ocean Acidification and Ocean Deoxygenation === <div id="h2-3-siblings" class="h2-siblings"></div> '''Ocean acidification is strengthening as a result of the ocean continuing to take up CO''' <sub>2</sub> '''from human-caused emissions''' ( ''very high confidence'' ''').''' This CO <sub>2</sub> uptake is driving changes in seawater chemistry that result in the decrease of pH and associated reductions in the saturation state of calcium carbonate, which is a constituent of skeletons or shells of a variety of marine organisms. These trends of ocean acidification are becoming clearer globally, with a ''very likely'' rate of decrease in pH in the ocean surface layer of 0.016 to 0.020 per decade in the subtropics and 0.002 to 0.026 per decade in subpolar and polar zones since the 1980s. Ocean acidification has spread deeper in the ocean, surpassing 2000 m depth in the northern North Atlantic and in the Southern Ocean. The greater projected pH declines in Coupled Model Intercomparison Project Phase 6 (CMIP6) models are primarily a consequence of higher atmospheric CO <sub>2</sub> concentrations in the Shared Socio-economic Pathways (SSPs) scenarios than their Coupled Model Intercomparison Project Phase 5 (CMIP5) Representative Concentration Pathway (RCP) analogues. {5.3.2.2, 5.3.3.1; 5.3.4.1; Figures 5.20, 5.21} '''Ocean deoxygenation is projected to continue to increase with ocean warming''' ( ''high confidence'' ''').''' Earth system models (ESMs) project a 32–71% greater subsurface (100–600 m) oxygen decline, depending on the scenario, than reported in the Special Report on the Ocean and Cryosphere (SROCC) for the period 2080–2099. This is attributed to the effect of larger surface warming in CMIP6 models, which increases ocean stratification and reduces ventilation ( ''medium confidence'' ). There is ''low confidence'' in the projected reduction of oceanic N <sub>2</sub> O emissions under high-emissions scenarios because of greater oxygen losses simulated in ESMs in CMIP6, uncertainties in the process of oceanic N <sub>2</sub> O emissions, and a limited number of modelling studies available. {5.3.3.2; 7.5} <div id="Future" class="h2-container"></div> <span id="future-projections-of-carbon-feedbacks-on-climate-change"></span> === Future Projections of Carbon Feedbacks on Climate Change === <div id="h2-4-siblings" class="h2-siblings"></div> '''Oceanic and terrestrial carbon sinks are projected to continue to grow with increasing atmospheric concentrations of CO''' <sub>2</sub> ''', but the fraction of emissions taken up by land and ocean is expected to decline as the CO''' <sub>2</sub> '''concentration increases''' ( ''high confidence'' ''').''' ESMs suggest approximately equal global land and ocean carbon uptake for each of the SSP scenarios. However, the range of model projections is much larger for the land carbon sink. Despite the wide range of model responses, uncertainty in atmospheric CO <sub>2</sub> by 2100 is dominated by future anthropogenic emissions rather than uncertainties related to carbon–climate feedbacks ( ''high confidence'' ). {5.4.5; Figure 5.25, 5.26} '''Increases in atmospheric CO''' <sub>2</sub> '''lead to increases in land carbon storage through CO''' <sub>2</sub> '''fertilization of photosynthesis and increased water use efficiency''' ( ''high confidence'' ''').''' However, the overall change in land carbon also depends on land-use change and on the response of vegetation and soil to continued warming and changes in the water cycle, including increased droughts in some regions that will diminish the sink capacity. Climate change alone is expected to increase land carbon accumulation in the high latitudes (not including permafrost) and also to lead to a counteracting loss of land carbon in the tropics ( ''medium confidence'' , Figure 5.25). More than half of the latest CMIP6 ESMs include nutrient limitations on the carbon cycle, but these models still project increasing tropical land carbon ( ''medium confidence'' ) and increasing global land carbon ( ''high confidence'' ) through the 21st century. {5.4.1, 5.4.3, 5.4.5; Figure 5.27; Cross-Chapter Box 5.1} '''Future trajectories of the ocean CO''' <sub>2</sub> '''sink are strongly emissions-scenario dependent''' ( ''high confidence'' ''').''' Emissions scenarios SSP4-6.0 and SSP5-8.5 lead to warming of the surface ocean and large reductions of the buffering capacity, which will slow the growth of the ocean sink after 2050. Scenario SSP1-2.6 limits further reductions in buffering capacity and warming, and the ocean sink weakens in response to the declining rate of increasing atmospheric CO <sub>2</sub> . There is ''low confidence'' in how changes in the biological pump will influence the magnitude and direction of the ocean carbon feedback. {5.4.2, 5.4.4, Cross-Chapter Box 5.3} '''Beyond 2100, land and ocean may transition from being a carbon sink to a source under either very high emissions or net negative emissions scenarios, but for different reasons.''' Under very high emissions scenarios such as SSP5-8.5, ecosystem carbon losses due to warming lead the land to transition from a carbon sink to a source ( ''medium confidence'' ), while the ocean is expected to remain a sink ( ''high confidence'' ). For scenarios in which CO <sub>2</sub> concentration stabilizes, land and ocean carbon sinks gradually take up less carbon as the increase in atmospheric CO <sub>2</sub> slows down. In scenarios with moderate net negative CO <sub>2</sub> emissions, and CO <sub>2</sub> concentrations declining during the 21st century (e.g., SSP1-2.6), the land sink transitions to a net source in decades to a few centuries after CO <sub>2</sub> emissions become net negative, while the ocean remains a sink ( ''low confidence'' ). Under scenarios with large net negative CO <sub>2</sub> emissions and rapidly declining CO <sub>2</sub> concentrations (e.g., SSP5-3.4-OS (overshoot)), both land and ocean switch from a sink to a transient source during the overshoot period ( ''medium confidence'' ). {5.4.10, 5.6.2.1.2; Figures 5.30, 5.33} '''Thawing terrestrial permafrost will lead to carbon release''' ( ''high confidence'' '''), but there is''' ''low confidence'' '''in the timing, magnitude and the relative roles of CO''' <sub>2</sub> '''versus CH''' <sub>4</sub> '''as feedback processes''' . CO <sub>2</sub> release from permafrost is projected to be 3–41 PgC per 1°C of global warming by 2100, based on an ensemble of models. However, the incomplete representation of important processes such as abrupt thaw, combined with weak observational constraints, only allow ''low confidence'' in both the magnitude of these estimates and in how linearly proportional this feedback is to the amount of global warming. It is ''very unlikely'' that gas clathrates in terrestrial and subsea permafrost will lead to a detectable departure from the emissions trajectory during this century. {5.4.9; Box 5.1} '''The net response of natural CH''' <sub>4</sub> '''and N''' <sub>2</sub> '''O sources to future warming will be increased emissions''' ( ''medium confidence'' ''').''' Key processes include increased CH <sub>4</sub> emissions from wetlands and permafrost thaw, as well as increased soil N <sub>2</sub> O emissions in a warmer climate, while ocean N <sub>2</sub> O emissions are projected to decline at centennial time scale. The magnitude of the responses of each individual process and how linearly proportional these feedbacks are to the amount of global warming is known with ''low confidence'' due to incomplete representation of important processes in models combined with weak observational constraints. Models project that, over the 21st century, the combined feedback of 0.02–0.09 W m <sup>–2</sup> °C <sup>–1</sup> is comparable to the effect of a CO <sub>2</sub> release of 5–18 petagrams of carbon equivalent per °C (PgCeq °C <sup>–1</sup> ) ( ''low confidence'' ). {5.4.7, 5.4.8; Figure 5.29} '''The response of biogeochemical cycles to the anthropogenic perturbation can be abrupt at regional scales, and irreversible on decadal to century time scales''' ( ''high confidence'' ''').''' The probability of crossing uncertain regional thresholds (e.g., high severity fires, forest dieback) increases with climate change ( ''high confidence'' ). Possible abrupt changes and tipping points in biogeochemical cycles lead to additional uncertainty in 21st century GHG concentrations, but these are ''very likely'' to be smaller than the uncertainty associated with future anthropogenic emissions ( ''high confi'' ''dence'' ). {5.4.9} <div id="Remaining" class="h2-container"></div> <span id="remaining-carbon-budgets-to-climate-stabilization"></span> === Remaining Carbon Budgets to Climate Stabilization === <div id="h2-5-siblings" class="h2-siblings"></div> '''There is a near-linear relationship between cumulative CO''' <sub>2</sub> '''emissions and the increase in global mean surface air temperature (GSAT) caused by CO''' <sub>2</sub> '''over the course of this century for global warming levels up to at least 2°C relative to pre-industrial''' ( ''high confidence'' ''').''' Halting global warming would thus require global net anthropogenic CO <sub>2</sub> emissions to become zero. The ratio between cumulative CO <sub>2</sub> emissions and the consequent GSAT increase, which is called the transient climate response to cumulative emissions of CO <sub>2</sub> (TCRE), ''likely'' falls in the 1.0°C–2.3°C per 1000 PgC range. The narrower range compared to the IPCC Fifth Assessment Report (AR5) is due to a better integration of evidence across the science in this assessment. Beyond this century, there is ''low confidence'' that the TCRE remains an accurate predictor of temperature changes in scenarios of very low or net negative CO <sub>2</sub> emissions because of uncertain Earth system feedbacks that can result in further warming or a path-dependency of warming as a function of cumulative CO <sub>2</sub> emissions. {5.4, 5.5.1} '''Mitigation requirements over this century for limiting maximum warming to specific levels can be quantified using a carbon budget that relates cumulative CO''' <sub>2</sub> '''emissions to global mean temperature increase''' ( ''high confidence'' ''').''' For the period 1850–2019, a total of 655 ± 65 PgC (2390 ± 240 GtCO <sub>2</sub> , ''likely'' range) of anthropogenic CO <sub>2</sub> has been emitted. Remaining carbon budgets (starting from 1 January 2020) for limiting warming to 1.5°C, 1.7°C, and 2.0°C are 140 PgC (500 GtCO <sub>2</sub> ), 230 PgC (850 GtCO <sub>2</sub> ) and 370 PgC (1350 GtCO <sub>2</sub> ), respectively, based on the 50th percentile of TCRE. For the 67th percentile, the respective values are 110 PgC (400 GtCO <sub>2</sub> ), 190 PgC (700 GtCO <sub>2</sub> ) and 310 PgC (1150 GtCO <sub>2</sub> ). These remaining carbon budgets may vary by an estimated ± 60 PgC (220 GtCO <sub>2</sub> ) depending on how successfully future non-CO <sub>2</sub> emissions can be reduced. Since AR5 and the Special Report on Global Warming of 1.5°C (SR1.5), estimates have undergone methodological improvements, resulting in larger, yet consistent estimates. {5.5.2, 5.6; Figure 5.31; Table 5.8} '''Several factors affect the precise value of remaining carbon budgets, including estimates of historical warming, future emissions from thawing permafrost, and variations in projected non-CO''' <sub>2</sub> '''warming.''' Remaining carbon budget estimates can increase or decrease by 150 PgC ( ''likely'' range; 150 PgC equals 550 GtCO <sub>2</sub> ) due to uncertainties in the level of historical warming, and by an additional ± 60 PgC (±220 GtCO, ''likely'' range) due to geophysical uncertainties surrounding the climate response to non-CO <sub>2</sub> emissions such as CH <sub>4</sub> , N <sub>2</sub> O, and aerosols. Permafrost thaw is included in the estimates, together with other feedbacks that are often not captured by models. Despite the large uncertainties surrounding the quantification of the effects of additional Earth system feedback processes, such as emissions from wetlands and permafrost thaw, these feedbacks represent identified additional amplifying risk factors that scale with additional warming and mostly increase the challenge of limiting warming to specific temperature thresholds. These uncertainties do not change the basic conclusion that global CO <sub>2</sub> emissions would need to decline to at least net zero to halt global warming. {5.4, 5.5.2} <div id="Biogeochemical" class="h2-container"></div> <span id="biogeochemical-implications-of-carbon-dioxide-removal-and-solar-radiation-modification"></span> === Biogeochemical Implications of Carbon Dioxide Removal and Solar Radiation Modification === <div id="h2-6-siblings" class="h2-siblings"></div> '''Land- and ocean-based carbon dioxide removal (CDR) methods have the potential to sequester CO''' <sub>2</sub> '''from the atmosphere, but the benefits of this removal would be partially offset by CO''' <sub>2</sub> '''release from land and ocean carbon stores''' ( ''very'' ''high confidence'' ''').''' The fraction of CO <sub>2</sub> removed that remains out of the atmosphere, a measure of CDR effectiveness, decreases slightly with increasing amount of removal ( ''medium confidence'' ) and decreases strongly if CDR is applied at lower CO <sub>2</sub> concentrations ( ''medium confidence'' ). {5.6.2.1; Figures 5.32, 5.33, 5.34} '''The century-scale climate–carbon cycle response to a CO''' <sub>2</sub> '''removal from the atmosphere is not always equal and opposite to the response to a CO''' <sub>2</sub> '''emission''' ( ''medium confidence'' ''').''' For simultaneously cumulative CO <sub>2</sub> emissions and removals of greater than or equal to 100 PgC, CO <sub>2</sub> emissions are 4 ± 3% more effective at raising atmospheric CO <sub>2</sub> than CO <sub>2</sub> removals are at lowering atmospheric CO <sub>2</sub> . The asymmetry originates from state-dependencies and non-linearities in carbon cycle processes and implies that an extra amount of CDR is required to compensate for a positive emission of a given magnitude to attain the same change in atmospheric CO <sub>2</sub> . The net effect of this asymmetry on the global surface temperature is poorly constrained due to ''low agreement'' between models ( ''low confidence'' ). {5.6.2.1; Figure 5.35} '''Wide-ranging side effects of CDR methods have been identified that can either weaken or strengthen the carbon sequestration and cooling potential of these methods and affect the achievement of sustainable development goals''' ( ''high confidence'' ''').''' Biophysical and biogeochemical side effects of CDR methods are associated with changes in surface albedo, the water cycle, emissions of CH <sub>4</sub> and N <sub>2</sub> O, ocean acidification and marine ecosystem productivity ( ''high confidence'' ). These side effects and associated Earth system feedbacks can decrease carbon uptake and/or change local and regional climate, and in turn limit the CO <sub>2</sub> sequestration and cooling potential of specific CDR methods ( ''medium confidence'' ). Deployment of CDR, particularly on land, can also affect water quality and quantity, food production and biodiversity, with consequences for the achievement of related sustainable development goals ( ''high confidence'' ). These effects are often highly dependent on local context, management regime, prior land use, and scale of deployment ( ''high confidence'' ). A wide range of co-benefits are obtained with methods that seek to restore natural ecosystems or improve soil carbon ( ''high confidence'' ). The biogeochemical effects of terminating CDR are expected to be small for most CDR methods ( ''medium confidence'' ). {5.6.2.2; Figure 5.36; Cross-Chapter Box 5.1} '''Solar radiation modification (SRM) would increase the global land and ocean CO''' <sub>2</sub> '''sinks''' ( ''medium confidence'' ''') but would not stop CO''' <sub>2</sub> '''from increasing in the atmosphere, thus exacerbating ocean acidification under continued anthropogenic emissions''' ( ''high confidence'' ''').''' SRM acts to cool the planet relative to unmitigated climate change, which would increase the land sink by reducing plant and soil respiration and slow the reduction of ocean carbon uptake due to warming ( ''medium confidence'' ). SRM would not counteract or stop ocean acidification ( ''high confidence'' ). The sudden and sustained termination of SRM would rapidly increase global warming, with the return of positive and negative effects on the carbon sinks ( ''very'' ''high confidence'' ). {4.6.3; 5.6.3} <div id="5.1" class="h1-container"></div> <span id="introduction"></span>
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