scholarly journals A global model study of the impact of land-use change in Borneo on atmospheric composition

2013 ◽  
Vol 13 (18) ◽  
pp. 9183-9194 ◽  
Author(s):  
N. J. Warwick ◽  
A. T. Archibald ◽  
K. Ashworth ◽  
J. Dorsey ◽  
P. M. Edwards ◽  
...  

Abstract. In this study, a high resolution version of the Cambridge p-TOMCAT chemical transport model is used, along with measurement data from the 2008 NERC-funded Oxidant and Particle Photochemical Processes (OP3) project, to examine the potential impact of the expansion of oil palm in Borneo on atmospheric composition. Several model emission scenarios are run for the OP3 measurement period, incorporating emissions from both global datasets and local flux measurements. Using the OP3 observed isoprene fluxes and OH recycling chemistry in p-TOMCAT substantially improves the comparison between modelled and observed isoprene and OH concentrations relative to using MEGAN isoprene emissions without OH recycling. However, a similar improvement was also achieved without using HOx recycling, by fixing boundary layer isoprene concentrations over Borneo to follow the OP3 observations. An extreme hypothetical future scenario, in which all of Borneo is converted to oil palm plantation, assessed the sensitivity of the model to changes in isoprene and NOx emissions associated with land-use change. This scenario suggested a 70% upper limit on surface ozone increases resulting from land-use change on Borneo, excluding the impact of future changes in emissions elsewhere. Although the largest changes in this scenario occurred directly over Borneo, the model also calculated notable regional changes of O3, OH and other species downwind of Borneo and in the free troposphere.


2013 ◽  
Vol 13 (3) ◽  
pp. 7431-7461 ◽  
Author(s):  
N. J. Warwick ◽  
A. T. Archibald ◽  
K. Ashworth ◽  
J. Dorsey ◽  
P. M. Edwards ◽  
...  

Abstract. In this study, we use a high resolution version of the Cambridge p-TOMCAT model, along with data collected during the 2008 NERC-funded Oxidant and Particle Photochemical Processes (OP3) project, to examine the potential impact of the expansion of oil palm in Borneo on air quality and atmospheric composition. Several model emission scenarios are run for the OP3 measurement period, incorporating emissions from both global datasets and local flux measurements. Isoprene fluxes observed at a forest site during OP3 were considerably less than fluxes calculated using the MEGAN model. Incorporating the observed isoprene fluxes into p-TOMCAT substantially improved the comparison between modelled and observed isoprene surface mixing ratios and OH concentrations relative to using the MEGAN emissions. If both observed isoprene fluxes and HOx recycling chemistry were included, the ability of the model to capture diurnal variations in isoprene and OH was further improved. However, a similar improvement was also achieved using a~standard chemical mechanism without HOx recycling, by fixing boundary layer isoprene concentrations over Borneo to follow the OP3 observations. Further model simulations, considering an extreme scenario with all of Borneo converted to oil palm plantation, were run to determine the maximum atmospheric impact of land use change in Borneo. In these simulations, the level of nitrogen oxides was found to be critical. If only isoprene emissions from oil palm are considered, then large scale conversion to oil palm produced a decrease in monthly mean surface ozone of up to ~20%. However, if related changes in NOx emissions from fertilisation, industrial processing and transport are also included then ozone increases of up to ~70% were calculated. Although the largest changes occurred locally, the model also calculated significant regional changes of O3, OH and other species downwind of Borneo and in the free troposphere.



2017 ◽  
Vol 17 (11) ◽  
pp. 6663-6678 ◽  
Author(s):  
Shreeya Verma ◽  
Julia Marshall ◽  
Mark Parrington ◽  
Anna Agustí-Panareda ◽  
Sebastien Massart ◽  
...  

Abstract. Airborne observations of greenhouse gases are a very useful reference for validation of satellite-based column-averaged dry air mole fraction data. However, since the aircraft data are available only up to about 9–13 km altitude, these profiles do not fully represent the depth of the atmosphere observed by satellites and therefore need to be extended synthetically into the stratosphere. In the near future, observations of CO2 and CH4 made from passenger aircraft are expected to be available through the In-Service Aircraft for a Global Observing System (IAGOS) project. In this study, we analyse three different data sources that are available for the stratospheric extension of aircraft profiles by comparing the error introduced by each of them into the total column and provide recommendations regarding the best approach. First, we analyse CH4 fields from two different models of atmospheric composition – the European Centre for Medium-Range Weather Forecasts (ECMWF) Integrated Forecasting System for Composition (C-IFS) and the TOMCAT/SLIMCAT 3-D chemical transport model. Secondly, we consider scenarios that simulate the effect of using CH4 climatologies such as those based on balloons or satellite limb soundings. Thirdly, we assess the impact of using a priori profiles used in the satellite retrievals for the stratospheric part of the total column. We find that the models considered in this study have a better estimation of the stratospheric CH4 as compared to the climatology-based data and the satellite a priori profiles. Both the C-IFS and TOMCAT models have a bias of about −9 ppb at the locations where tropospheric vertical profiles will be measured by IAGOS. The C-IFS model, however, has a lower random error (6.5 ppb) than TOMCAT (12.8 ppb). These values are well within the minimum desired accuracy and precision of satellite total column XCH4 retrievals (10 and 34 ppb, respectively). In comparison, the a priori profile from the University of Leicester Greenhouse Gases Observing Satellite (GOSAT) Proxy XCH4 retrieval and climatology-based data introduce larger random errors in the total column, being limited in spatial coverage and temporal variability. Furthermore, we find that the bias in the models varies with latitude and season. Therefore, applying appropriate bias correction to the model fields before using them for profile extension is expected to further decrease the error contributed by the stratospheric part of the profile to the total column.



2016 ◽  
Author(s):  
Sam J. Silva ◽  
Colette L. Heald ◽  
Jeffrey A. Geddes ◽  
Kemen G. Austin ◽  
Prasad S. Kasibhatla ◽  
...  

Abstract. Over recent decades oil palm plantations have rapidly expanded across Southeast Asia (SEA). According to the United Nations, oil palm production in SEA increased by a factor of 3 from 1995 to 2010. We investigate the impacts of current (2010) and future (2020) oil palm expansion in SEA on surface-atmosphere exchange and the resulting air quality in the region. For this purpose, we use satellite data, high-resolution land maps, and the chemical transport model GEOS-Chem. Relative to a no oil palm plantation scenario (~ 1990), overall simulated isoprene emissions in the region increase by 13 % due to oil palm plantations in 2010 and a further 11 % by 2020. In addition, the expansion of palm plantations leads to local increases in ozone deposition velocities of up to 20 %. The net result of these changes is that oil palm expansion in SEA increases surface O3 by up to 3.5 ppbv over dense urban regions, and could rise more than 4.5 ppbv above baseline levels by 2020. Biogenic secondary organic aerosol loadings also increase by up to 1 μg m−3 due to oil palm expansion, and could increase a further 2.5 μg m−3 by 2020. Our analysis indicates that while the impact of recent oil palm expansion on air quality in the region has been significant, the retrieval error and sensitivity of the current constellation of satellite measurements limit our ability to observe these impacts from space. Oil palm expansion is likely to continue to degrade air quality in the region in the coming decade and hinder efforts to achieve air quality regulations in major urban areas such as Kuala Lumpur and Singapore.



2011 ◽  
Vol 366 (1582) ◽  
pp. 3210-3224 ◽  
Author(s):  
J. A. Pyle ◽  
N. J. Warwick ◽  
N. R. P. Harris ◽  
Mohd Radzi Abas ◽  
A. T. Archibald ◽  
...  

We present results from the OP3 campaign in Sabah during 2008 that allow us to study the impact of local emission changes over Borneo on atmospheric composition at the regional and wider scale. OP3 constituent data provide an important constraint on model performance. Treatment of boundary layer processes is highlighted as an important area of model uncertainty. Model studies of land-use change confirm earlier work, indicating that further changes to intensive oil palm agriculture in South East Asia, and the tropics in general, could have important impacts on air quality, with the biggest factor being the concomitant changes in NO x emissions. With the model scenarios used here, local increases in ozone of around 50 per cent could occur. We also report measurements of short-lived brominated compounds around Sabah suggesting that oceanic (and, especially, coastal) emission sources dominate locally. The concentration of bromine in short-lived halocarbons measured at the surface during OP3 amounted to about 7 ppt, setting an upper limit on the amount of these species that can reach the lower stratosphere.



2016 ◽  
Vol 16 (4) ◽  
pp. 1937-1953 ◽  
Author(s):  
Gregory R. Wentworth ◽  
Jennifer G. Murphy ◽  
Betty Croft ◽  
Randall V. Martin ◽  
Jeffrey R. Pierce ◽  
...  

Abstract. Continuous hourly measurements of gas-phase ammonia (NH3(g)) were taken from 13 July to 7 August 2014 on a research cruise throughout Baffin Bay and the eastern Canadian Arctic Archipelago. Concentrations ranged from 30 to 650 ng m−3 (40–870 pptv) with the highest values recorded in Lancaster Sound (74°13′ N, 84°00′ W). Simultaneous measurements of total ammonium ([NHx]), pH and temperature in the ocean and in melt ponds were used to compute the compensation point (χ), which is the ambient NH3(g) concentration at which surface–air fluxes change direction. Ambient NH3(g) was usually several orders of magnitude larger than both χocean and χMP (< 0.4–10 ng m3) indicating these surface pools are net sinks of NH3. Flux calculations estimate average net downward fluxes of 1.4 and 1.1 ng m−2 s−1 for the open ocean and melt ponds, respectively. Sufficient NH3(g) was present to neutralize non-sea-salt sulfate (nss-SO42−) in the boundary layer during most of the study. This finding was corroborated with a historical data set of PM2.5 composition from Alert, Nunavut (82°30′ N, 62°20′ W) wherein the median ratio of NH4+/nss-SO42− equivalents was greater than 0.75 in June, July and August. The GEOS-Chem chemical transport model was employed to examine the impact of NH3(g) emissions from seabird guano on boundary-layer composition and nss-SO42− neutralization. A GEOS-Chem simulation without seabird emissions underestimated boundary layer NH3(g) by several orders of magnitude and yielded highly acidic aerosol. A simulation that included seabird NH3 emissions was in better agreement with observations for both NH3(g) concentrations and nss-SO42− neutralization. This is strong evidence that seabird colonies are significant sources of NH3 in the summertime Arctic, and are ubiquitous enough to impact atmospheric composition across the entire Baffin Bay region. Large wildfires in the Northwest Territories were likely an important source of NH3, but their influence was probably limited to the Central Canadian Arctic. Implications of seabird-derived N-deposition to terrestrial and aquatic ecosystems are also discussed.



2018 ◽  
Vol 11 (10) ◽  
pp. 4103-4116 ◽  
Author(s):  
Liye Zhu ◽  
Maria Val Martin ◽  
Luciana V. Gatti ◽  
Ralph Kahn ◽  
Arsineh Hecobian ◽  
...  

Abstract. Biomass burning is a significant source of trace gases and aerosols to the atmosphere, and the evolution of these species depends acutely on where they are injected into the atmosphere. GEOS-Chem is a chemical transport model driven by assimilated meteorological data that is used to probe a variety of scientific questions related to atmospheric composition, including the role of biomass burning. This paper presents the development and implementation of a new global biomass burning emissions injection scheme in the GEOS-Chem model. The new injection scheme is based on monthly gridded Multi-angle Imaging SpectroRadiometer (MISR) global plume-height stereoscopic observations in 2008. To provide specific examples of the impact of the model updates, we compare the output from simulations with and without the new MISR-based injection height scheme to several sets of observations from regions with active fires. Our comparisons with Arctic Research on the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) aircraft observations show that the updated injection height scheme can improve the ability of the model to simulate the vertical distribution of peroxyacetyl nitrate (PAN) and carbon monoxide (CO) over North American boreal regions in summer. We also compare a simulation for October 2010 and 2011 to vertical profiles of CO over the Amazon Basin. When coupled with larger emission factors for CO, a simulation that includes the new injection scheme also better matches selected observations in this region. Finally, the improved injection height improves the simulation of monthly mean surface CO over California during July 2008, a period with large fires.



2003 ◽  
Vol 3 (1) ◽  
pp. 551-596 ◽  
Author(s):  
D. S. Stevenson ◽  
C. E. Johnson ◽  
E. J. Highwood ◽  
V. Gauci ◽  
W. J. Collins ◽  
...  

Abstract. Results from the first chemistry-transport model study of the impact of the 1783–1784 Laki fissure eruption (Iceland: 64° N, 17° W) upon atmospheric composition are presented. The eruption released an estimated 122 Tg(SO2) into the troposphere and lower stratosphere. The model has a high resolution tropopause region, and detailed sulphur chemistry. The simulated SO2 plume spreads over much of the Northern Hemisphere, polewards of ~40° N. About 70% of the SO2 gas is directly deposited to the surface before it can be oxidised to sulphuric acid aerosol. The main SO2 oxidants, OH and H2O2 , are depleted by up to 40% zonally, and the lifetime of SO2 consequently in-creases. Zonally averaged tropospheric SO2 concentrations over the first three months of the eruption exceed 20 ppbv, and sulphuric acid aerosol reaches ~2 ppbv. A total aerosol yield of 51–66 Tg(H2SO4 ) is produced. The mean aerosol lifetime is only 6–9 days, and the peak aerosol loading of the atmosphere is only ~7 Tg(H2SO4.2H2O). Due to the relatively short atmospheric residence times of both the SO2 and sulphate, the aerosol loading approximately mirrors the temporal evolution of emissions associated with the eruption. The model produces a reasonable simulation of the acid deposition found in Greenland ice cores. These results appear to be relatively insensitive to the vertical profile of emissions assumed, although if more of the emissions reached higher levels (>12 km), this would give longer lifetimes and larger aerosol yields. This study suggests that most previous estimates of the global aerosol loading associated with Laki have been generally too large in magnitude, and too long-lived. Environmental effects following the Laki eruption may have been dominated by the widespread deposition of SO2 gas rather than sulphuric acid aerosol.



2016 ◽  
Vol 16 (23) ◽  
pp. 14997-15010 ◽  
Author(s):  
Colette L. Heald ◽  
Jeffrey A. Geddes

Abstract. Anthropogenic land use change (LUC) since preindustrial (1850) has altered the vegetation distribution and density around the world. We use a global model (GEOS-Chem) to assess the attendant changes in surface air quality and the direct radiative forcing (DRF). We focus our analysis on secondary particulate matter and tropospheric ozone formation. The general trend of expansion of managed ecosystems (croplands and pasturelands) at the expense of natural ecosystems has led to an 11 % decline in global mean biogenic volatile organic compound emissions. Concomitant growth in agricultural activity has more than doubled ammonia emissions and increased emissions of nitrogen oxides from soils by more than 50 %. Conversion to croplands has also led to a widespread increase in ozone dry deposition velocity. Together these changes in biosphere–atmosphere exchange have led to a 14 % global mean increase in biogenic secondary organic aerosol (BSOA) surface concentrations, a doubling of surface aerosol nitrate concentrations, and local changes in surface ozone of up to 8.5 ppb. We assess a global mean LUC-DRF of +0.017, −0.071, and −0.01 W m−2 for BSOA, nitrate, and tropospheric ozone, respectively. We conclude that the DRF and the perturbations in surface air quality associated with LUC (and the associated changes in agricultural emissions) are substantial and should be considered alongside changes in anthropogenic emissions and climate feedbacks in chemistry–climate studies.



2019 ◽  
Author(s):  
Emanuele Emili ◽  
Brice Barret ◽  
Eric Le Flochmoën ◽  
Daniel Cariolle

Abstract. The prior information used for Level 2 (L2) retrievals in the thermal infrared can influence the quality of the retrievals themselves and, therefore, their further assimilation in atmospheric composition models. In this study we evaluate the differences between assimilating L2 ozone profiles and Level 1 (L1) radiances from the Infrared Atmospheric Sounding Interferometer (IASI). We minimized potential differences between the two approaches by employing the same radiative transfer code (RTTOV) and a very similar setup for both the L2 retrievals (1D-Var) and the L1 assimilation (3D-Var). We computed hourly 3D-Var reanalyses assimilating respectively L1 and L2 data in the chemical transport model MOCAGE and compared the resulting O3 fields among each other and against ozonesondes. We also evaluated the joint assimilation of limb measurements from the Microwave Limb Sounder (MLS) on top of IASI to assess the impact of stratospheric O3 on tropospheric reanalyses. Results indicate that significant differences can arise between L2 and L1 assimilation, especially in regions where the L2 prior is biased (at the tropics and in the southern hemisphere in this study). L1 and L2 assimilation give instead very similar results in the northern hemisphere, especially when MLS measurements are used to constrain the stratospheric O3 column. We conclude this study by listing remaining issues that are common to both the L1 and L2 approaches and that deserve further research.



2016 ◽  
Author(s):  
Shreeya Verma ◽  
Julia Marshall ◽  
Mark Parrington ◽  
Anna Agusti-Panareda ◽  
Sebastien Massart ◽  
...  

Abstract. Airborne observations of greenhouse gases are a very useful reference for validation of satellite-based column-averaged dry air mole fraction data. However, since the aircraft data are available only up to about 9–13 km altitude, these profiles do not fully represent the depth of the atmosphere observed by satellites and therefore need to be extended synthetically into the stratosphere. In the near future, observations of CO2 and CH4 made from passenger aircraft are expected to be available through the In-Service Aircraft for a Global Observing System (IAGOS) project. In this study, we analyse three different data sources that are available for the stratospheric extension of aircraft profiles by comparing the error introduced by each of them into the total column and provide recommendations regarding the best approach. First, we analyse CH4 fields from two different models of atmospheric composition – the European Centre for Medium-Range Weather Forecasts (ECMWF) Integrated Forecasting System for Composition (C-IFS) and the TOMCAT/SLIMCAT 3-D chemical transport model. Secondly, we consider scenarios that simulate the effect of using CH4 climatologies such as those based on balloons or satellite limb soundings. Thirdly, we assess the impact of using a-priori profiles used in the satellite retrievals for the stratospheric part of the total column. We find that the models considered in this study have a better estimation of the stratospheric CH4 as compared to the climatology-based data and the satellite a-priori profiles. Both the C-IFS and TOMCAT models have a bias of about −9 ppb at the locations where tropospheric vertical profiles will be measured by IAGOS. The C-IFS model, however, has a lower random error (6.5 ppb) than TOMCAT (12.8 ppb). These values are well within the minimum desired accuracy and precision of satellite total column XCH4 retrievals (10 ppb and 34 ppb, respectively). In comparison, the a-priori profile from the University of Leicester Greenhouse Gases Observing Satellite (GOSAT) Proxy XCH4 retrieval and climatology-based data introduce larger random errors in the total column, being limited in spatial coverage and temporal variability. Furthermore, we find that the bias in the models varies with latitude and season. Therefore, applying appropriate bias correction to the model fields before using them for profile extension is expected to further decrease the error contributed by the stratospheric part of the profile to the total column.



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