scholarly journals Hindcasting and forecasting of regional methane from coal mine emissions in the Upper Silesian Coal Basin using the online nested global regional chemistry–climate model MECO(n) (MESSy v2.53)

2020 ◽  
Vol 13 (4) ◽  
pp. 1925-1943 ◽  
Author(s):  
Anna-Leah Nickl ◽  
Mariano Mertens ◽  
Anke Roiger ◽  
Andreas Fix ◽  
Axel Amediek ◽  
...  
Keyword(s):  
Coal Mining ◽  
Spatial Resolution ◽  
Radiative Forcing ◽  
Climate Model ◽  
Mitigation Strategies ◽  
Climate Mitigation ◽  
Coal Basin ◽  
Airborne Measurements ◽  
Upper Silesian Coal Basin ◽  
The Impact

Abstract. Methane is the second most important greenhouse gas in terms of anthropogenic radiative forcing. Since pre-industrial times, the globally averaged dry mole fraction of methane in the atmosphere has increased considerably. Emissions from coal mining are one of the primary anthropogenic methane sources. However, our knowledge about different sources and sinks of methane is still subject to great uncertainties. Comprehensive measurement campaigns and reliable chemistry–climate models, are required to fully understand the global methane budget and to further develop future climate mitigation strategies. The CoMet 1.0 campaign (May to June 2018) combined airborne in situ, as well as passive and active remote sensing measurements to quantify the emissions from coal mining in the Upper Silesian Coal Basin (USCB, Poland). Roughly 502 kt of methane is emitted from the ventilation shafts per year. In order to help with the flight planning during the campaigns, we performed 6 d forecasts using the online coupled, three-time nested global and regional chemistry–climate model MECO(n). We applied three-nested COSMO/MESSy instances going down to a spatial resolution of 2.8 km over the USCB. The nested global–regional model system allows for the separation of local emission contributions from fluctuations in the background methane. Here, we introduce the forecast set-up and assess the impact of the model's spatial resolution on the simulation of methane plumes from the ventilation shafts. Uncertainties in simulated methane mixing ratios are estimated by comparing different airborne measurements to the simulations. Results show that MECO(3) is able to simulate the observed methane plumes and the large-scale patterns (including vertically integrated values) reasonably well. Furthermore, we obtain reasonable forecast results up to forecast day four.

scholarly journals Forecasting of regional methane from coal mine emissions in the Upper Silesian Coal Basin using the on-line nested global regional chemistry climate model MECO(n)(MESSy v2.53)

2019 ◽  
Author(s):  
Anna-Leah Nickl ◽  
Mariano Mertens ◽  
Anke Roiger ◽  
Andreas Fix ◽  
Axel Amediek ◽  
...  
Keyword(s):  
Coal Mining ◽  
Radiative Forcing ◽  
Large Scale ◽  
Climate Models ◽  
Climate Model ◽  
Mitigation Strategies ◽  
Climate Mitigation ◽  
Coal Basin ◽  
Upper Silesian Coal Basin ◽  
On Line

Abstract. Methane is the second most important greenhouse gas in terms of anthropogenic radiative forcing. Since pre-industrial times, the globally averaged dry mole fraction of methane in the atmosphere has increased considerably. Emissions from coal mining are one of the primary anthropogenic methane sources. However, our knowledge about different sources and sinks of methane is still subject to great uncertainties. Comprehensive measuring campaigns, as well as reliable chemistry climate models, are required to fully understand the global methane budget and to further develop future climate mitigation strategies. The CoMet 1.0 campaign (May to June 2018) combined airborne in-situ, as well as passive and active remote sensing measurements to quantify the emissions from coal mining in the Upper Silesian Coal Basin (USCB, Poland). Roughly 502 kt of methane are emitted from the ventilation shafts per year. In order to help the campaigns flight planning, we performed 6-day forecasts using the on-line coupled, three times nested global and regional chemistry climate model MECO(n). We applied three nested COSMO/MESSy instances going down to a spatial resolution of 2.8 km over the USCB. The nested global/regional model system allows for the separation of local emission contributions from fluctuations in the background methane. Here we introduce the forecast setup and assess the model skill by comparing different observations with the individual forecast simulations. Results show that MECO(3) is able to simulate the observed methane plumes and the large scale patterns (including vertically integrated values) reasonably well. Furthermore we receive reasonable forecast results up to forecast day four.

scholarly journals Sensitivity of black carbon concentrations and climate impact to aging and scavenging

2016 ◽  
Author(s):  
Marianne T. Lund ◽  
Terje K. Berntsen ◽  
Bjørn H. Samset
Keyword(s):  
Nitric Acid ◽  
Black Carbon ◽  
Radiative Forcing ◽  
Mitigation Strategies ◽  
The Arctic ◽  
Climate Mitigation ◽  
Vertical Profiles ◽  
The Impact ◽  
Model Measurement ◽  
Global Mean

Abstract. Despite recent improvements, significant uncertainties in global modeling of black carbon (BC) aerosols persist, posing important challenges for the design and evaluation of effective climate mitigation strategies targeted at BC emission reductions. Here we investigate the sensitivity of BC concentrations in the chemistry-transport model OsloCTM2 with the microphysical aerosol parameterization M7 (OsloCTM2-M7) to parameters controlling aerosol aging and scavenging. We focus on Arctic surface concentrations and remote region BC vertical profiles, and introduce a novel treatment of condensation of nitric acid on BC. The OsloCTM2-M7 underestimates annual averaged BC surface concentrations, with a mean normalized bias of −0.55. The seasonal cycle and magnitude of Arctic BC surface concentrations is improved compared to previous OsloCTM2 studies, but model-measurement discrepancies during spring remain. High-altitude BC over the Pacific is overestimated compared with measurements from the HIPPO campaigns. We find that a shorter global BC lifetime improves the agreement with HIPPO, in line with other recent studies. Several processes can achieve this, including allowing for convective scavenging of hydrophobic BC and reducing the amount of soluble material required for aging. Simultaneously, the concentrations in the Arctic are reduced, resulting in poorer agreement with measurements in part of the region. A first step towards inclusion of aging by nitrate in OsloCTM2-M7 is made by allowing for condensation of nitric acid on BC. This results in a faster aging and reduced lifetime, and in turn to a better agreement with the HIPPO measurements. On the other hand, model-measurement discrepancies in the Arctic are exacerbated. Work to further improve this parameterization is needed. The impact on global mean radiative forcing (RF) and surface temperature response (TS) in our experiments is estimated. Compared to the baseline, decreases in global mean direct RF on the order of 10–30 % of the total pre-industrial to present BC direct RF is estimated for the experiments that result in the largest changes in BC concentrations. We show that globally tuning parameters related to BC aging and scavenging can improve the representation of BC vertical profiles in the OsloCTM2-M7 compared with observations. Our results also show that such improvements can result from changes in several processes and often depend on assumptions about uncertain parameters such as the BC ice nucleating efficiency and the change in hygroscopicity with aging. It is also important to be aware of potential tradeoffs in model performance between different regions. Other important sources of uncertainty, particularly for Arctic BC, such as model resolution has not been investigated here. Our results underline the importance of more observations and experimental data to improve process understanding and thus further constrain models.

scholarly journals Global sensitivity of aviation NO<sub>x</sub> effects to the HNO<sub>3</sub>-forming channel of the HO<sub>2</sub>+NO reaction

2012 ◽  
Vol 12 (9) ◽  
pp. 24287-24349
Author(s):  
K. Gottschaldt ◽  
C. Voigt ◽  
P. Jöckel ◽  
M. Righi ◽  
R. Deckert ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Radiative Forcing ◽  
Climate Model ◽  
Rate Coefficient ◽  
Climate Impact ◽  
Mitigation Strategies ◽  
Global Sensitivity ◽  
Mixing Ratios ◽  
Modelling Studies ◽  
The Impact

Abstract. The impact of a recently proposed HNO3-forming channel of the HO2+NO reaction (Butkovskaya et al., 2005, 2007) on atmospheric mixing ratios of ozone, methane and their precursors is assessed with a global stratosphere-troposphere chemistry-climate model. Previous modelling studies applied a rate coefficient that depends only on pressure and temperature. We additionally considered a possible enhancement of the reaction by humidity, as found by a laboratory study (Butkovskaya et al., 2009). This particularly reduces the oxidation capacity of the atmosphere, increasing methane lifetime significantly. The effects of aircraft NOx emissions on atmospheric chemistry are altered when considering the above reaction, resulting in a negative net radiative forcing relative to an atmosphere without aviation NOx. Uncertainties associated with the inclusion of the HO2+NO → HNO3 reaction and with its corresponding rate coefficient propagate a considerable additional uncertainty on estimates of the climate impact of aviation and on NOx-related mitigation strategies.

scholarly journals Middle atmosphere response to the solar cycle in irradiance and ionizing particle precipitation

2011 ◽  
Vol 11 (10) ◽  
pp. 5045-5077 ◽  
Author(s):  
K. Semeniuk ◽  
V. I. Fomichev ◽  
J. C. McConnell ◽  
C. Fu ◽  
S. M. L. Melo ◽  
...  
Keyword(s):  
Solar Cycle ◽  
Radiative Forcing ◽  
Climate Model ◽  
Middle Atmosphere ◽  
High Energy ◽  
Galactic Cosmic Rays ◽  
Particle Precipitation ◽  
Solar Cycle Variation ◽  
Cycle Variation ◽  
The Impact

Abstract. The impact of NOx and HOx production by three types of energetic particle precipitation (EPP), auroral zone medium and high energy electrons, solar proton events and galactic cosmic rays on the middle atmosphere is examined using a chemistry climate model. This process study uses ensemble simulations forced by transient EPP derived from observations with one-year repeating sea surface temperatures and fixed chemical boundary conditions for cases with and without solar cycle in irradiance. Our model results show a wintertime polar stratosphere ozone reduction of between 3 and 10 % in agreement with previous studies. EPP is found to modulate the radiative solar cycle effect in the middle atmosphere in a significant way, bringing temperature and ozone variations closer to observed patterns. The Southern Hemisphere polar vortex undergoes an intensification from solar minimum to solar maximum instead of a weakening. This changes the solar cycle variation of the Brewer-Dobson circulation, with a weakening during solar maxima compared to solar minima. In response, the tropical tropopause temperature manifests a statistically significant solar cycle variation resulting in about 4 % more water vapour transported into the lower tropical stratosphere during solar maxima compared to solar minima. This has implications for surface temperature variation due to the associated change in radiative forcing.

scholarly journals Exploring the uncertainties in the aviation soot–cirrus effect

2021 ◽  
Vol 21 (23) ◽  
pp. 17267-17289
Author(s):  
Mattia Righi ◽  
Johannes Hendricks ◽  
Christof Gerhard Beer
Keyword(s):  
Radiative Forcing ◽  
Climate Model ◽  
Internal Variability ◽  
Reanalysis Data ◽  
Ice Nucleation ◽  
Cirrus Clouds ◽  
Model Studies ◽  
Model Dynamics ◽  
Analogous Model ◽  
The Impact

Abstract. A global aerosol–climate model, including a two-moment cloud microphysical scheme and a parametrization for aerosol-induced ice formation in cirrus clouds, is applied in order to quantify the impact of aviation soot on natural cirrus clouds. Several sensitivity experiments are performed to assess the uncertainties in this effect related to (i) the assumptions on the ice nucleation abilities of aviation soot, (ii) the representation of vertical updrafts in the model, and (iii) the use of reanalysis data to relax the model dynamics (the so-called nudging technique). Based on the results of the model simulations, a radiative forcing from the aviation soot–cirrus effect in the range of −35 to 13 mW m−2 is quantified, depending on the assumed critical saturation ratio for ice nucleation and active fraction of aviation soot but with a confidence level below 95 % in several cases. Simple idealized experiments with prescribed vertical velocities further show that the uncertainties on this aspect of the model dynamics are critical for the investigated effect and could potentially add a factor of about 2 of further uncertainty to the model estimates of the resulting radiative forcing. The use of the nudging technique to relax model dynamics is proved essential in order to identify a statistically significant signal from the model internal variability, while simulations performed in free-running mode and with prescribed sea-surface temperatures and sea-ice concentrations are shown to be unable to provide robust estimates of the investigated effect. A comparison with analogous model studies on the aviation soot–cirrus effect show a very large model diversity, with a conspicuous lack of consensus across the various estimates, which points to the need for more in-depth analyses on the roots of such discrepancies.

scholarly journals Impact of biogenic hydrocarbons on tropospheric chemistry: results from a global chemistry-climate model

2005 ◽  
Vol 5 (5) ◽  
pp. 10517-10612 ◽  
Author(s):  
G. A. Folberth ◽  
D. A. Hauglustaine ◽  
J. Lathière ◽  
F. Brocheton
Keyword(s):  
Tropospheric Ozone ◽  
Radiative Forcing ◽  
Climate Model ◽  
Primary Source ◽  
Tropospheric Chemistry ◽  
Secondary Source ◽  
Peroxy Radicals ◽  
Substantial Impact ◽  
The Impact ◽  
Global Mean

Abstract. We present a description and evaluation of LMDz-INCA, a global three-dimensional chemistry-climate model, pertaining to its recently developed NMHC version. In this substantially extended version of the model a comprehensive representation of the photochemistry of non-methane hydrocarbons (NMHC) and volatile organic compounds (VOC) from biogenic, anthropogenic, and biomass-burning sources has been included. The tropospheric annual mean methane (9.2 years) and methylchloroform (5.5 years) chemical lifetimes are well within the range of previous modelling studies and are in excellent agreement with estimates established by means of global observations. The model provides a reasonable simulation of the horizontal and vertical distribution and seasonal cycle of CO and key non-methane VOC, such as acetone, methanol, and formaldehyde as compared to observational data from several ground stations and aircraft campaigns. LMDz-INCA in the NMHC version reproduces tropospheric ozone concentrations fairly well throughout most of the troposphere. The model is applied in several sensitivity studies of the biosphere-atmosphere photochemical feedback. The impact of surface emissions of isoprene, acetone, and methanol is studied. These experiments show a substantial impact of isoprene on tropospheric ozone and carbon monoxide concentrations revealing an increase in surface O3 and CO levels of up to 30 ppbv and 60 ppbv, respectively. Isoprene also appears to significantly impact the global OH distribution resulting in a decrease of the global mean tropospheric OH concentration by approximately 0.9×105 molecules cm−3 or roughly 10% and an increase in the global mean tropospheric methane lifetime by approximately four months. A global mean ozone net radiative forcing due to the isoprene induced increase in the tropospheric ozone burden of 0.09W m−2 is found. The key role of isoprene photooxidation in the global tropospheric redistribution of NOx is demonstrated. LMDz-INCA calculates an increase of PAN surface mixing ratios ranging from 75 to 750 pptv and 10 to 250 pptv during northern hemispheric summer and winter, respectively. Acetone and methanol are found to play a significant role in the upper troposphere/lower stratosphere (UT/LS) budget of peroxy radicals. Calculations with LMDz-INCA show an increase in HOx concentrations region of 8 to 15% and 10 to 15% due to methanol and acetone biogenic surface emissions, respectively. The model has been used to estimate the global tropospheric CO budget. A global CO source of 3019 TgCO yr−1 is estimated. This source divides into a primary source of 1533 TgCO yr−1 and secondary source of 1489 TgCO yr−1 deriving from VOC photooxidation. Global VOC-to-CO conversion efficiencies of 90% for methane and between 20 and 45% for individual VOC are calculated by LMDz-INCA.

Some future projections from coupling the U.K. Earth System Model to the Antarctic ice sheets

2021 ◽  
Author(s):  
Anthony Siahaan
Keyword(s):  
Radiative Forcing ◽  
Climate Model ◽  
Ice Sheet ◽  
Mass Gain ◽  
Ice Shelves ◽  
Positive Effects ◽  
Basal Melting ◽  
The Antarctic ◽  
The Impact ◽  
Increasing Precipitation

&lt;p&gt;A UKESM climate model which is coupled annually to the BISICLES ice sheet model to enable a two way interactions in Antarctica has been developed&amp;#160;&lt;br&gt;and run through a small ensemble of four SSP1-1.9 &amp; SSP5-8.5 scenario members. Under the extreme anthropogenic forcing, all the initial condition&amp;#160;&lt;br&gt;ensemble members develop strong melting under the cold &amp; large Ross and Filchner-Ronne ice-shelves, where it starts after the first half of simulation&amp;#160;&lt;br&gt;period for the former and in the last decade of the run for the latter. Despite that, during the 85 years timescale of these scenario runs, the stronger radiative forcing has positive effects on the ice-sheet mass gain through increasing precipitation on grounded ice regions which offsets the impact of basal melting in ice discharge across the grounding lines.&lt;/p&gt;

scholarly journals Radiative forcing estimates of sulfate aerosol in coupled climate-chemistry models with emphasis on the role of the temporal variability

2012 ◽  
Vol 12 (12) ◽  
pp. 5583-5602 ◽  
Author(s):  
C. Déandreis ◽  
Y. Balkanski ◽  
J. L. Dufresne ◽  
A. Cozic
Keyword(s):  
Temporal Variability ◽  
Radiative Forcing ◽  
Climate Model ◽  
Circulation Model ◽  
Reference Method ◽  
Sulfate Aerosol ◽  
The Impact ◽  
Net Fluxes ◽  
Indirect Radiative Forcing ◽  
Aerosol Radiative

Abstract. This paper describes the impact on the sulfate aerosol radiative effects of coupling the radiative code of a global circulation model with a chemistry-aerosol module. With this coupling, temporal variations of sulfate aerosol concentrations influence the estimate of aerosol radiative impacts. Effects of this coupling have been assessed on net fluxes, radiative forcing and temperature for the direct and first indirect effects of sulfate. The direct effect respond almost linearly to rapid changes in concentrations whereas the first indirect effect shows a strong non-linearity. In particular, sulfate temporal variability causes a modification of the short wave net fluxes at the top of the atmosphere of +0.24 and +0.22 W m−2 for the present and preindustrial periods, respectively. This change is small compared to the value of the net flux at the top of the atmosphere (about 240 W m−2). The effect is more important in regions with low-level clouds and intermediate sulfate aerosol concentrations (from 0.1 to 0.8 μg (SO4) m−3 in our model). The computation of the aerosol direct radiative forcing is quite straightforward and the temporal variability has little effect on its mean value. In contrast, quantifying the first indirect radiative forcing requires tackling technical issues first. We show that the preindustrial sulfate concentrations have to be calculated with the same meteorological trajectory used for computing the present ones. If this condition is not satisfied, it introduces an error on the estimation of the first indirect radiative forcing. Solutions are proposed to assess radiative forcing properly. In the reference method, the coupling between chemistry and climate results in a global average increase of 8% in the first indirect radiative forcing. This change reaches 50% in the most sensitive regions. However, the reference method is not suited to run long climate simulations. We present other methods that are simpler to implement in a coupled chemistry/climate model and that offer the possibility to assess radiative forcing.

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