RESUMEN
The control of the production of ozone-depleting substances through the Montreal Protocol means that the stratospheric ozone layer is recovering1 and that consequent increases in harmful surface ultraviolet radiation are being avoided2,3. The Montreal Protocol has co-benefits for climate change mitigation, because ozone-depleting substances are potent greenhouse gases4-7. The avoided ultraviolet radiation and climate change also have co-benefits for plants and their capacity to store carbon through photosynthesis8, but this has not previously been investigated. Here, using a modelling framework that couples ozone depletion, climate change, damage to plants by ultraviolet radiation and the carbon cycle, we explore the benefits of avoided increases in ultraviolet radiation and changes in climate on the terrestrial biosphere and its capacity as a carbon sink. Considering a range of strengths for the effect of ultraviolet radiation on plant growth8-12, we estimate that there could have been 325-690 billion tonnes less carbon held in plants and soils by the end of this century (2080-2099) without the Montreal Protocol (as compared to climate projections with controls on ozone-depleting substances). This change could have resulted in an additional 115-235 parts per million of atmospheric carbon dioxide, which might have led to additional warming of global-mean surface temperature by 0.50-1.0 degrees. Our findings suggest that the Montreal Protocol may also be helping to mitigate climate change through avoided decreases in the land carbon sink.
Asunto(s)
Secuestro de Carbono , Pérdida de Ozono/prevención & control , Ozono Estratosférico/análisis , Dióxido de Carbono/análisis , Secuestro de Carbono/efectos de la radiación , Calentamiento Global/prevención & control , Calentamiento Global/estadística & datos numéricos , Historia del Siglo XXI , Fotosíntesis/efectos de la radiación , Plantas/metabolismo , Plantas/efectos de la radiación , Temperatura , Rayos UltravioletaRESUMEN
Climate simulations that consider injection into the atmosphere of 15,000 Tg of soot, the amount estimated to be present at the Cretaceous-Paleogene boundary, produce what might have been one of the largest episodes of transient climate change in Earth history. The observed soot is believed to originate from global wildfires ignited after the impact of a 10-km-diameter asteroid on the Yucatán Peninsula 66 million y ago. Following injection into the atmosphere, the soot is heated by sunlight and lofted to great heights, resulting in a worldwide soot aerosol layer that lasts several years. As a result, little or no sunlight reaches the surface for over a year, such that photosynthesis is impossible and continents and oceans cool by as much as 28 °C and 11 °C, respectively. The absorption of light by the soot heats the upper atmosphere by hundreds of degrees. These high temperatures, together with a massive injection of water, which is a source of odd-hydrogen radicals, destroy the stratospheric ozone layer, such that Earth's surface receives high doses of UV radiation for about a year once the soot clears, five years after the impact. Temperatures remain above freezing in the oceans, coastal areas, and parts of the Tropics, but photosynthesis is severely inhibited for the first 1 y to 2 y, and freezing temperatures persist at middle latitudes for 3 y to 4 y. Refugia from these effects would have been very limited. The transient climate perturbation ends abruptly as the stratosphere cools and becomes supersaturated, causing rapid dehydration that removes all remaining soot via wet deposition.
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Molecules of the ß-diketone and ß-dialdehyde families were trapped in solid parahydrogen (pH2) to investigate the vibrational behavior of systems containing an intramolecular hydrogen bond (IHB). In the simplest ß-diketone, acetylacetone (AcAc), H transfer related to the IHB is coupled with methyl torsions. In pH2, the study of nuclear spin conversion (NSC) in methyl groups allows the characterisation of the influence of these large amplitude motions on the vibrational modes. The deuteration of the OH group involved in the IHB has important consequences on the vibrational spectrum of the molecule and evidence of NSC in methyl groups is difficult to obtain. In the chlorine derivative (3-chloroacetylacetone), the H-transfer is no longer coupled with methyl torsion, and NSC has undetectable effects on the IR spectrum. A search of H tunnelling splitting in the IR spectra of ß-dialdehydes trapped in pH2 was performed. A few modes of 2-chloromalonaldehyde appear as doublets and were assigned to tunnelling levels. The spectroscopic results related to large amplitude motions are detailed and discussed, highlighting puzzling effects.
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The photochemistry of the chelated enol form of acetylacetone (AcAc) was investigated by UV excitation of the S(2) state at 266 nm in parahydrogen matrices, complemented by experiments in neon and normal hydrogen matrices. Infrared (IR) spectroscopy, combined with theoretical calculations, was used to identify the photoproducts. Isomerization towards various non-chelated forms (no intramolecular H-bond) of AcAc is the dominant channel whereas fragmentation is very minor. The isomerization kinetics is monitored by IR spectroscopy. Among the seven non-chelated conformers of AcAc, only three are formed in parahydrogen matrices, whereas four are observed in normal hydrogen matrices. This difference suggests that an active tunnelling process between conformers occurs in parahydrogen but is quenched in normal hydrogen where guest-host interactions are stronger. Fragmentation and isomerization of excited AcAc are discussed in the light of these new data. The role of the intermediate triplet state in the S(2)â S(0) relaxation is confirmed, as the importance of phonons in the condensed phase.
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Hidrógeno/química , Pentanonas/aislamiento & purificación , Cinética , Pentanonas/química , Fotoquímica , Teoría Cuántica , Espectroscopía Infrarroja por Transformada de Fourier , Rayos UltravioletaRESUMEN
A noteworthy example of a molecule with coupled large-amplitude motions is provided by acetylacetone (methyl group torsions and intramolecular hydrogen bonds). The molecule was trapped in solid parahydrogen to investigate the complex proton tunneling processes. Nuclear spin conversion in methyl groups is observed and, combined with IR spectra, documents the coupling between high frequency modes and large amplitude motions.
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We examine the thermal structure of the mesosphere and lower thermosphere (MLT) using observations from 2002 through 2021 from the SABER instrument on the NASA TIMED satellite. These observations show that the MLT has significantly cooled and contracted between the years 2002 and 2019 (the year of the most recent solar minimum) due to a combination of a decline in the intensity of the 11-year solar cycle and increasing carbon dioxide (CO2.) During this time the thickness of atmosphere between the 1 and 10-4 hPa pressure surfaces (approximately 48 and 105 km) has contracted by 1,333 m, of which 342 m is attributed to increasing CO2. All other pressure surfaces in the MLT have similarly contracted. We further postulate that the MLT in the two most recent solar minima (2008-2009 and 2019-2020) was very likely the coldest and thinnest since the beginning of the Industrial Age. The sensitivity of the MLT to a doubling of CO2 is shown to be -7.5 K based on observed trends in temperature and growth rates of CO2. Colder temperatures observed at 10-4 hPa in 2019 than in the prior solar minimum in 2009 may be due to a decrease of 5% in solar irradiance in the Schumann-Runge band spectral region (175-200 nm).
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In 2016, the westerly quasi-biennial oscillation (WQBO) in the equatorial stratosphere was unprecedentedly disrupted by westward forcing near 40 hPa; this was followed by another disruption in 2020. Strong extratropical Rossby waves propagating toward the tropics were considered the main cause of the disruptions, but why the zonal wind is reversed only in the middle of the WQBO remains unclear. Here, we show that strong westerly winds in the equatorial lower stratosphere (70 to 100 hPa) help to disrupt the WQBO by hindering the wind reversal at its base. They also help equatorial westward waves propagate further upward, increasing the negative forcing at around 40 hPa that drives the QBO disruptions. Tropical westerly winds have been increasing in the past and are projected to increase in a warmer climate. These background wind changes may allow more frequent QBO disruptions in the future, leading to less predictability in atmospheric weather and climate systems.
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The Brewer-Dobson Circulation (BDC) determines the distribution of long-lived tracers in the stratosphere; therefore, their changes can be used to diagnose changes in the BDC. We evaluate decadal (2005-2018) trends of nitrous oxide (N2O) in two versions of the Whole Atmosphere Chemistry-Climate Model (WACCM) by comparing them with measurements from four Fourier transform infrared (FTIR) ground-based instruments, the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS), and with a chemistry-transport model (CTM) driven by four different reanalyses. The limited sensitivity of the FTIR instruments can hide negative N2O trends in the mid-stratosphere because of the large increase in the lowermost stratosphere. When applying ACE-FTS measurement sampling on model datasets, the reanalyses from the European Center for Medium Range Weather Forecast (ECMWF) compare best with ACE-FTS, but the N2O trends are consistently exaggerated. The N2O trends obtained with WACCM disagree with those obtained from ACE-FTS, but the new WACCM version performs better than the previous above the Southern Hemisphere in the stratosphere. Model sensitivity tests show that the decadal N2O trends reflect changes in the stratospheric transport. We further investigate the N2O Transformed Eulerian Mean (TEM) budget in WACCM and in the CTM simulation driven by the latest ECMWF reanalysis. The TEM analysis shows that enhanced advection affects the stratospheric N2O trends in the Tropics. While no ideal observational dataset currently exists, this model study of N2O trends still provides new insights about the BDC and its changes because of the contribution from relevant sensitivity tests and the TEM analysis.
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We use a chemistry-climate model and new estimates of smoke produced by fires in contemporary cities to calculate the impact on stratospheric ozone of a regional nuclear war between developing nuclear states involving 100 Hiroshima-size bombs exploded in cities in the northern subtropics. We find column ozone losses in excess of 20% globally, 25-45% at midlatitudes, and 50-70% at northern high latitudes persisting for 5 years, with substantial losses continuing for 5 additional years. Column ozone amounts remain near or <220 Dobson units at all latitudes even after three years, constituting an extratropical "ozone hole." The resulting increases in UV radiation could impact the biota significantly, including serious consequences for human health. The primary cause for the dramatic and persistent ozone depletion is heating of the stratosphere by smoke, which strongly absorbs solar radiation. The smoke-laden air rises to the upper stratosphere, where removal mechanisms are slow, so that much of the stratosphere is ultimately heated by the localized smoke injections. Higher stratospheric temperatures accelerate catalytic reaction cycles, particularly those of odd-nitrogen, which destroy ozone. In addition, the strong convection created by rising smoke plumes alters the stratospheric circulation, redistributing ozone and the sources of ozone-depleting gases, including N(2)O and chlorofluorocarbons. The ozone losses predicted here are significantly greater than previous "nuclear winter/UV spring" calculations, which did not adequately represent stratospheric plume rise. Our results point to previously unrecognized mechanisms for stratospheric ozone depletion.
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Modelos Químicos , Guerra Nuclear , Ozono , Movimientos del Aire , Atmósfera , Clorofluorocarburos , Óxidos de Nitrógeno , Humo , Rayos UltravioletaRESUMEN
Anthropogenic forcing of the atmosphere by greenhouse gases (GHG) and ozone-depleting substances has provided an unintended test of the robustness of current understanding of the physics and chemistry of the middle atmosphere, that is, the stratosphere and mesosphere. We explore this topic by examining how well anthropogenic changes can be simulated by modern, comprehensive numerical models. Specifically, we discuss the simulations of trends in global mean temperature; the development of the ozone hole and its impact on the dynamics of the Southern Hemisphere, both in the stratosphere and troposphere; trends in the stratospheric Brewer-Dobson circulation; and the response of the quasi-biennial oscillation (QBO) to increasing burdens of CO2 . We find that, in most of these cases, numerical simulation is able to reproduce observed changes and provide physical insights into the relevant mechanisms. Simulation of the QBO is on a less firm footing. Although many numerical models can now generate realistic QBOs, future projections of its behavior under the increasing burdens of GHG are inconsistent and even contradictory.
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Efectos Antropogénicos , Atmósfera , Gases de Efecto Invernadero , Humanos , Modelos Teóricos , TemperaturaRESUMEN
Although the El Niño-Southern Oscillation (ENSO) is a tropospheric phenomenon, its effects are also observed in the stratosphere. Traditionally, the study of ENSO above the troposphere has been difficult because of the lack of global observations at high altitudes and also because of the presence of other sources of variability whose signals are difficult to disentangle from ENSO effects. Recent work with general circulation models that isolate the ENSO signal have demonstrated its upward propagation into the stratosphere. Here we review the literature in this field and show results from the most recent version of the Whole Atmosphere Community Climate Model to illustrate the propagation and the mechanisms whereby the signal manifests itself in the stratosphere. The ENSO signal propagates upward to about 40 km by means of large-scale Rossby waves. The propagation is strongly influenced by the zonal mean zonal winds. Most of the strong ENSO events tend to peak in the boreal winter and so the ENSO signal is observed mainly at high latitudes during the Northern Hemisphere winter where the winds are westerly and allow Rossby wave propagation. The ENSO signal is also identified at polar latitudes in the Northern Hemisphere winter in the form of warmer temperatures and weaker winds during a strong El Niño event. This signal shows a zonally homogeneous behavior from the intensification of the stratospheric meridional circulation (in which air rises in the tropics and moves toward the winter pole where it descends) forced by anomalous propagation and dissipation of Rossby waves at middle latitudes during strong ENSO events.
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We provide an overview of geoengineering by stratospheric sulphate aerosols. The state of understanding about this topic as of early 2008 is reviewed, summarizing the past 30 years of work in the area, highlighting some very recent studies using climate models, and discussing methods used to deliver sulphur species to the stratosphere. The studies reviewed here suggest that sulphate aerosols can counteract the globally averaged temperature increase associated with increasing greenhouse gases, and reduce changes to some other components of the Earth system. There are likely to be remaining regional climate changes after geoengineering, with some regions experiencing significant changes in temperature or precipitation. The aerosols also serve as surfaces for heterogeneous chemistry resulting in increased ozone depletion. The delivery of sulphur species to the stratosphere in a way that will produce particles of the right size is shown to be a complex and potentially very difficult task. Two simple delivery scenarios are explored, but similar exercises will be needed for other suggested delivery mechanisms. While the introduction of the geoengineering source of sulphate aerosol will perturb the sulphur cycle of the stratosphere signicantly, it is a small perturbation to the total (stratosphere and troposphere) sulphur cycle. The geoengineering source would thus be a small contributor to the total global source of 'acid rain' that could be compensated for through improved pollution control of anthropogenic tropospheric sources. Some areas of research remain unexplored. Although ozone may be depleted, with a consequent increase to solar ultraviolet-B (UVB) energy reaching the surface and a potential impact on health and biological populations, the aerosols will also scatter and attenuate this part of the energy spectrum, and this may compensate the UVB enhancement associated with ozone depletion. The aerosol will also change the ratio of diffuse to direct energy reaching the surface, and this may influence ecosystems. The impact of geoengineering on these components of the Earth system has not yet been studied. Representations for the formation, evolution and removal of aerosol and distribution of particle size are still very crude, and more work will be needed to gain confidence in our understanding of the deliberate production of this class of aerosols and their role in the climate system.
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Atmósfera/química , Clima , Conservación de los Recursos Naturales/métodos , Ecosistema , Ingeniería/tendencias , Efecto Invernadero , Sulfatos/química , Aerosoles/química , Desastres/prevención & controlRESUMEN
This paper reports on an investigation into the chronology of El Niño/Southern Oscillation (ENSO) events during the period from the arrival of Europeans in Perú in 1531 until the year 1841 when conventional barometricdata became available in the tropical regions. A number of probable ENSO events can be dated from anecdotal reports of significant rainfall in the coastal desert of northern Perú. In many of the years with anomalous Peruvian rainfall it is also possible to use various types pf proxy data to identify aspects of the global teleconnection patterns usually associated with tropical ENSO events(AU)