Academic literature on the topic 'Tropospheric ozone, climate change, forest, BVOC emission'
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Journal articles on the topic "Tropospheric ozone, climate change, forest, BVOC emission"
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Yu, H., J. K. Holopainen, M. Kivimäenpää, A. Virtanen, and J. D. Blande. "Potential of Climate Change and Herbivory to Affect the Release and Atmospheric Reactions of BVOCs from Boreal and Subarctic Forests." Molecules 26, no. 8 (April 15, 2021): 2283. http://dx.doi.org/10.3390/molecules26082283.
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Compared to most other forest ecosystems, circumpolar boreal and subarctic forests have few tree species, and are prone to mass outbreaks of herbivorous insects. A short growing season with long days allows rapid plant growth, which will be stimulated by predicted warming of polar areas. Emissions of biogenic volatile organic compounds (BVOC) from soil and vegetation could be substantial on sunny and warm days and biotic stress may accelerate emission rates. In the atmosphere, BVOCs are involved in various gas-phase chemical reactions within and above forest canopies. Importantly, the oxidation of BVOCs leads to secondary organic aerosol (SOA) formation. SOA particles scatter and absorb solar radiation and grow to form cloud condensation nuclei (CCN) and participate in cloud formation. Through BVOC and moisture release and SOA formation and condensation processes, vegetation has the capacity to affect the abiotic environment at the ecosystem scale. Recent BVOC literature indicates that both temperature and herbivory have a major impact on BVOC emissions released by woody species. Boreal conifer forest is the largest terrestrial biome and could be one of the largest sources of biogenic mono- and sesquiterpene emissions due to the capacity of conifer trees to store terpene-rich resins in resin canals above and belowground. Elevated temperature promotes increased diffusion of BVOCs from resin stores. Moreover, insect damage can break resin canals in needles, bark, and xylem and cause distinctive bursts of BVOCs during outbreaks. In the subarctic, mountain birch forests have cyclic outbreaks of Geometrid moths. During outbreaks, trees are often completely defoliated leading to an absence of BVOC-emitting foliage. However, in the years following an outbreak there is extended shoot growth, a greater number of leaves, and greater density of glandular trichomes that store BVOCs. This can lead to a delayed chemical defense response resulting in the highest BVOC emission rates from subarctic forest in the 1–3 years after an insect outbreak. Climate change is expected to increase insect outbreaks at high latitudes due to warmer seasons and arrivals of invasive herbivore species. Increased BVOC emission will affect tropospheric ozone (O3) formation and O3 induced oxidation of BVOCs. Herbivore-induced BVOC emissions from deciduous and coniferous trees are also likely to increase the formation rate of SOA and further growth of the particles in the atmosphere. Field experiments measuring the BVOC emission rates, SOA formation rate and particle concentrations within and above the herbivore attacked forest stands are still urgently needed.
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Harper, Kandice L., and Nadine Unger. "Global climate forcing driven by altered BVOC fluxes from 1990 to 2010 land cover change in maritime Southeast Asia." Atmospheric Chemistry and Physics 18, no. 23 (November 30, 2018): 16931–52. http://dx.doi.org/10.5194/acp-18-16931-2018.
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Abstract. Over the period of 1990–2010, maritime Southeast Asia experienced large-scale land cover changes, including expansion of high-isoprene-emitting oil palm plantations and contraction of low-isoprene-emitting natural forests. The ModelE2-Yale Interactive terrestrial Biosphere global chemistry–climate model is used to quantify the atmospheric composition changes, and for the first time, the associated radiative forcing induced by the land-cover-change-driven biogenic volatile organic compound (BVOC) emission changes (+6.5 TgC y−1 isoprene, −0.5 TgC y−1 monoterpenes). Regionally, surface-level ozone concentrations largely decreased (−3.8 to +0.8 ppbv). The tropical land cover changes occurred in a region of strong convective transport, providing a mechanism for the BVOC perturbations to affect the composition of the upper troposphere. Enhanced concentrations of isoprene and its degradation products are simulated in the upper troposphere, and, on a global-mean basis, land cover change had a stronger impact on ozone in the upper troposphere (+0.5 ppbv) than in the lower troposphere (<0.1 ppbv increase). The positive climate forcing from ozone changes (+9.2 mW m−2) was partially offset by a negative forcing (−0.8 mW m−2) associated with an enhancement in secondary organic aerosol (SOA). The sign of the net forcing is sensitive to uncertainty in the SOA yield from BVOCs. The global-mean ozone forcing per unit of regional oil palm expansion is +1 mW m−2 Mha−1. In light of expected continued expansion of oil palm plantations, regional land cover changes may play an increasingly important role in driving future global ozone radiative forcing.
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Wang, Hui, Qizhong Wu, Alex B. Guenther, Xiaochun Yang, Lanning Wang, Tang Xiao, Jie Li, Jinming Feng, Qi Xu, and Huaqiong Cheng. "A long-term estimation of biogenic volatile organic compound (BVOC) emission in China from 2001–2016: the roles of land cover change and climate variability." Atmospheric Chemistry and Physics 21, no. 6 (March 29, 2021): 4825–48. http://dx.doi.org/10.5194/acp-21-4825-2021.
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Abstract. Satellite observations reveal that China has been leading the global greening trend in the past 2 decades. We assessed the impact of land cover change as well as climate variability on total biogenic volatile organic compound (BVOC) emission in China from 2001–2016. We found the greening trend in China is leading a national-scale increase in BVOC emission. The BVOC emission level in 2016 could be 11.7 % higher than that in 2001 because of higher tree cover fraction and vegetation biomass. On the regional scale, the BVOC emission level from 2013–2016 could be 8.6 %–19.3 % higher than that from 2001–2004 in hotspots including (1) northeastern China, (2) Beijing and its surrounding areas, (3) the Qin Mountains, (4) Yunnan Province, (5) Guangxi–Guangdong provinces, and (6) Hainan island because of the land cover change without considering the impact of climate variability. The comparison among different scenarios showed that vegetation changes resulting from land cover management are the main driver of BVOC emission change in China. Climate variability contributed significantly to interannual variations but not much to the changing trend during the study period. In the standard scenario, which considers both land cover change and climate variability, a statistically significant increasing trend can still be found in regions including Beijing and its surroundings, Yunnan Province, and Hainan island, and BVOC emission total amount in these regions from 2013–2016 is 11.0 %–17.2 % higher that from 2001–2004. We compared the long-term HCHO vertical columns (VC) from the satellite-based Ozone Monitoring Instrument (OMI) with the estimation of isoprene emission in summer. The results showed statistically significant positive correlation coefficients over the regions with high vegetation cover fractions. In addition, the isoprene emission and HCHO VC both showed statistically significant increasing trends in the south of China where these two variables have high positive correlation coefficients. This result may support our estimation of the variability and trends of BVOC emission in this region; however, the comparison still has large uncertainties since the chemical and physical processes, including transportation, diffusion and chemical reactions, were not considered. Our results suggest that the continued increase in BVOC will enhance the importance of considering BVOC when making policies for controlling ozone pollution in China along with ongoing efforts to increase the forest cover fraction.
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Saunier, Amélie, Elena Ormeño, Christophe Boissard, Henri Wortham, Brice Temime-Roussel, Caroline Lecareux, Alexandre Armengaud, and Catherine Fernandez. "Effect of mid-term drought on <i>Quercus pubescens</i> BVOCs' emission seasonality and their dependency on light and/or temperature." Atmospheric Chemistry and Physics 17, no. 12 (June 22, 2017): 7555–66. http://dx.doi.org/10.5194/acp-17-7555-2017.
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Abstract. Biogenic volatile organic compounds (BVOCs) emitted by plants represent a large source of carbon compounds released into the atmosphere, where they account for precursors of tropospheric ozone and secondary organic aerosols. Being directly involved in air pollution and indirectly in climate change, understanding what factors drive BVOC emissions is a prerequisite for modeling their emissions and predict air pollution. The main algorithms currently used to model BVOC emissions are mainly light and/or temperature dependent. Additional factors such as seasonality and drought also influence isoprene emissions, especially in the Mediterranean region, which is characterized by a rather long drought period in summer. These factors are increasingly included in models but only for the principal studied BVOC, namely isoprene, but there are still some discrepancies in estimations of emissions. In this study, the main BVOCs emitted by Quercus pubescens – isoprene, methanol, acetone, acetaldehyde, formaldehyde, MACR, MVK and ISOPOOH (these three last compounds detected under the same m∕z) – were monitored with a PTR-ToF-MS over an entire seasonal cycle during both in situ natural and amplified drought, which is expected with climate change. Amplified drought impacted all studied BVOCs by reducing emissions in spring and summer while increasing emissions in autumn. All six BVOCs monitored showed daytime light and temperature dependencies while three BVOCs (methanol, acetone and formaldehyde) also showed emissions during the night despite the absence of light under constant temperature. Moreover, methanol and acetaldehyde burst in the early morning and formaldehyde deposition and uptake were also punctually observed, which were not assessed by the classical temperature and light models.
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Schurgers, G., T. Hickler, P. A. Miller, and A. Arneth. "European emissions of isoprene and monoterpenes from the Last Glacial Maximum to present." Biogeosciences Discussions 6, no. 5 (September 3, 2009): 8805–49. http://dx.doi.org/10.5194/bgd-6-8805-2009.
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Abstract. Biogenic volatile organic compounds (BVOC), such as isoprene and monoterpenes, play an important role in atmospheric processes. BVOC species are oxidized in the atmosphere and influence levels of ozone. The less volatile amongst the BVOC and their oxidation products are important for the formation and growth of secondary biogenic aerosol. In this way, the earth's radiation balance is affected. Geographic distribution and temporal changes in BVOC emissions are highly uncertain. Here we assessed changes in emission patterns across Europe since the Last Glacial Maximum (LGM) with a dynamic vegetation model that reproduces European tree species distribution and in which a process-based algorithm for terpenoid production was incorporated. In a set of simulations the model was driven with paleoclimate anomalies and reconstructed CO2 concentrations. We quantified three main driving factors for the changes in emissions of isoprene and monoterpenes since the LGM: (1) the changes in climate, with temperature changes as the most important factor affecting plant physiology and terpenoid production in all plant species, (2) a change in species distribution related to the changes in climate, causing local shifts in emission characteristics of the vegetation, and (3) a change in CO2 concentration, causing opposing effects on the availability of different substrates for terpenoid production. The effect of atmospheric CO2 concentration is particularly uncertain, but sensitivity simulations showed an increase in European BVOC emissions in all sensitivity experiments irrespective of the use of a direct inhibition of terpenoid production by CO2. The effects of climate change on physiology and terpenoid production resulted in an overall relatively uniform increase of emissions in Europe over the simulation period, but regionally the effect of changes in species distribution and the related changes in emission capacities resulted in changes of emissions that can dominate over the physiology effects. This may have consequences for regional atmospheric chemistry simulations for the past, that have to rely on suitable geographic patterns of forest emissions.
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Schurgers, G., T. Hickler, P. A. Miller, and A. Arneth. "European emissions of isoprene and monoterpenes from the Last Glacial Maximum to present." Biogeosciences 6, no. 12 (December 3, 2009): 2779–97. http://dx.doi.org/10.5194/bg-6-2779-2009.
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Abstract. Biogenic volatile organic compounds (BVOC), such as isoprene and monoterpenes, play an important role in atmospheric processes. BVOC species are oxidized in the atmosphere and influence levels of ozone. The less volatile amongst the BVOC and their oxidation products are important for the formation and growth of secondary biogenic aerosol. In this way, the Earth's radiation balance is affected. Geographic distribution and temporal changes in BVOC emissions are highly uncertain. Here we assessed changes in emission patterns across Europe since the Last Glacial Maximum (LGM) with a dynamic vegetation model. This model reproduces European tree species distribution and includes a process-based algorithm for terpenoid production. In a set of simulations the model was driven with paleoclimate anomalies and reconstructed CO2 concentrations. We quantified three main driving factors for the changes in emissions of isoprene and monoterpenes since the LGM: (1) the changes in climate, with temperature changes as the most important factor affecting plant physiology and terpenoid production in all plant species, (2) a change in species distribution related to the changes in climate, causing local shifts in emission characteristics of the vegetation, and (3) a change in CO2 concentration, causing opposing effects on the availability of different substrates for terpenoid production. The effect of atmospheric CO2 concentration is particularly uncertain, but sensitivity simulations showed an increase in European BVOC emissions in all sensitivity experiments irrespective of the use of a direct inhibition of terpenoid production by CO2. The effects of climate change on physiology and terpenoid production resulted in an overall relatively uniform increase of emissions in Europe over the simulation period, but regionally the effect of changes in species distribution and the related changes in emission capacities resulted in changes of emissions that can dominate over the physiology effects. This may have consequences for regional atmospheric chemistry simulations for the past, that have to rely on suitable geographic patterns of forest emissions.
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Wang, Hui, Qizhong Wu, Hongjun Liu, Yuanlin Wang, Huaqiong Cheng, Rongrong Wang, Lanning Wang, Han Xiao, and Xiaochun Yang. "Sensitivity of biogenic volatile organic compound emissions to leaf area index and land cover in Beijing." Atmospheric Chemistry and Physics 18, no. 13 (July 9, 2018): 9583–96. http://dx.doi.org/10.5194/acp-18-9583-2018.
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Abstract. The Beijing area has suffered from severe air pollution in recent years, including ozone pollution in the summer. In addition to the anthropogenic emissions inventory, understanding local ozone pollution requires a reliable biogenic volatile organic compound (BVOC) emission inventory. Forest coverage rose from 20.6 to 35.8 % from 1998 to 2013 in Beijing according to the National Forest Resource Survey (NFRS), and accurate representations of land cover for recent years is crucial for estimating BVOC emissions and their impacts on air quality. In this study, we established a high-resolution BVOC emission inventory in Beijing using the Model of Emissions of Gases and Aerosols from Nature (MEGAN) v2.1 with three independent leaf area index (LAI) products and three independent land cover products. Various combinations of the Global LAnd Surface Satellite (GLASS), Moderate-Resolution Imaging Spectroradiometer (MODIS) MCD15, and GEOland (GEO) v2 LAI datasets and the Finer Resolution Observation and Monitoring of Global Land Cover (FROM-GLC), MODIS MCD12Q1 plant functional type (PFT) products, and Climate Change Initiative Land Cover (CCI LC) products are used in five model sensitivity experiments (E1–E5), and the experiment using the FROM-GLC with the highest spatial resolution of 30 m and GLASS LAI products was treated as the baseline. These sensitivity calculations were driven by hourly, 3 km meteorological fields from the Weather Research and Forecasting (WRF) model. The following results were obtained: (1) according to the baseline estimate, the total amount of BVOC emissions is 75.9 Gg for the Beijing area, and isoprene, monoterpenes, sesquiterpenes and other VOCs account for 37.6, 14.6, 1.8 and 46 % of the total, respectively. Approximately three-quarters of BVOC emissions occur in the summer. (2) According to the sensitivity experiments, the LAI input does not significantly affect the BVOC emissions. Using MODIS MCD15Q1 and GEO v2 LAI led to slight declines of 2.6 and 1.4 %, respectively, of BVOC emissions in the same area. (3) The spatial distribution of PFTs from different inputs strongly influenced the spatial distribution of BVOC emissions. Furthermore, the cross-walking table for converting land cover classes to PFTs also has a strong impact on BVOC emissions; the sensitivity experiments showed that the estimate of BVOC emissions by CCI LC ranged from 42.1 to 70.2 Gg depending on the cross-walking table used.
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Thorp, Thomas, Stephen R. Arnold, Richard J. Pope, Dominick V. Spracklen, Luke Conibear, Christoph Knote, Mikhail Arshinov, et al. "Late-spring and summertime tropospheric ozone and NO<sub>2</sub> in western Siberia and the Russian Arctic: regional model evaluation and sensitivities." Atmospheric Chemistry and Physics 21, no. 6 (March 25, 2021): 4677–97. http://dx.doi.org/10.5194/acp-21-4677-2021.
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Abstract. We use a regional chemistry transport model (Weather Research and Forecasting model coupled with chemistry, WRF-Chem) in conjunction with surface observations of tropospheric ozone and Ozone Monitoring Instrument (OMI) satellite retrievals of tropospheric column NO2 to evaluate processes controlling the regional distribution of tropospheric ozone over western Siberia for late spring and summer in 2011. This region hosts a range of anthropogenic and natural ozone precursor sources, and it serves as a gateway for near-surface transport of Eurasian pollution to the Arctic. However, there is a severe lack of in situ observations to constrain tropospheric ozone sources and sinks in the region. We show widespread negative bias in WRF-Chem tropospheric column NO2 when compared to OMI satellite observations from May–August, which is reduced when using ECLIPSE (Evaluating the Climate and Air Quality Impacts of Short-Lived Pollutants) v5a emissions (fractional mean bias (FMB) = −0.82 to −0.73) compared with the EDGAR (Emissions Database for Global Atmospheric Research)-HTAP (Hemispheric Transport of Air Pollution) v2.2 emissions data (FMB = −0.80 to −0.70). Despite the large negative bias, the spatial correlations between model and observed NO2 columns suggest that the spatial pattern of NOx sources in the region is well represented. Scaling transport and energy emissions in the ECLIPSE v5a inventory by a factor of 2 reduces column NO2 bias (FMB = −0.66 to −0.35), but with overestimates in some urban regions and little change to a persistent underestimate in background regions. Based on the scaled ECLIPSE v5a emissions, we assess the influence of the two dominant anthropogenic emission sectors (transport and energy) and vegetation fires on surface NOx and ozone over Siberia and the Russian Arctic. Our results suggest regional ozone is more sensitive to anthropogenic emissions, particularly from the transport sector, and the contribution from fire emissions maximises in June and is largely confined to latitudes south of 60∘ N. Ozone dry deposition fluxes from the model simulations show that the dominant ozone dry deposition sink in the region is to forest vegetation, averaging 8.0 Tg of ozone per month, peaking at 10.3 Tg of ozone deposition during June. The impact of fires on ozone dry deposition within the domain is small compared to anthropogenic emissions and is negligible north of 60∘ N. Overall, our results suggest that surface ozone in the region is controlled by an interplay between seasonality in atmospheric transport patterns, vegetation dry deposition, and a dominance of transport and energy sector emissions.
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Duhl, T. R., D. Gochis, A. Guenther, S. Ferrenberg, and E. Pendall. "Emissions of BVOC from Lodgepole Pine in response to Mountain Pine Beetle attack in high and low mortality forest stands." Biogeosciences Discussions 9, no. 7 (July 24, 2012): 9125–67. http://dx.doi.org/10.5194/bgd-9-9125-2012.
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Abstract. In this screening study biogenic volatile organic compound (BVOC) emissions from intact branches of lodgepole pine (Pinus contorta) trees were measured from trees at two forested sites that have been impacted differently by the mountain pine beetle (MPB) with one having higher mortality and the other with lower mortality. Differences in the amounts and chemical diversity of BVOC between the two sites and from apparently healthy trees versus trees in different stages of MPB attack are presented, as well as (for one site) observed seasonal variability in emissions. A brief site comparison is made of the hydrological characteristics and prior disturbances (both natural and man-made) at the sites. Trees sampled at the site experiencing high MPB-related tree mortality had lower chemodiversity in terms of monoterpene (MT) emission profiles, while profiles were more diverse at the lower-mortality site. Also at the higher-mortality site, MPB-infested trees in various stages of decline had lower emissions of sesquiterpenes (SQT) compared to healthy trees, while at the site with lower mortality, MPB-survivors had significantly higher SQT emissions during part of the growing season when compared to both uninfested and newly-infested trees. SQT profiles differed between the two sites, and, like monoterpene and oxygenated VOC profiles, varied through the season For the low-mortality site in which repeated measurements were made over the course the early summer-late fall, higher chemical diversity was observed in early- compared to late-season measurements for all compound classes investigated (MT, oxygenated VOC, and SQT), with the amount of change appearing to correlate to the MPB status of the trees studied. Emissions of methyl-3-buten-2-ol had a distinct seasonal signal but were not much different between healthy or infested trees, except in trees with dead needles, from which emissions of this compound were negligible, and in late-season MPB survivors, in which they were higher than in newly-infested or uninfested trees. Emissions of SQT were significantly higher in the MPB survivors during both mid- and late-season sampling at the low-mortality site. The changes in emissions could have implications for regional air quality and climate through changes in ozone and aerosol distributions, although this study was designed as a preliminary screening effort and not enough individuals were sampled for all of the observed differences to be statistically demonstrated. Despite this, the compelling differences in emissions observed between the sites and individual trees with differing MPB-infestation statuses and the potential impacts these have on regional atmospheric chemistry argue for further research in this topic.
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Duhl, T. R., D. Gochis, A. Guenther, S. Ferrenberg, and E. Pendall. "Emissions of BVOC from lodgepole pine in response to mountain pine beetle attack in high and low mortality forest stands." Biogeosciences 10, no. 1 (January 25, 2013): 483–99. http://dx.doi.org/10.5194/bg-10-483-2013.
Full textAbstract:
Abstract. In this screening study, biogenic volatile organic compound (BVOC) emissions from intact branches of lodgepole pine (Pinus contorta) trees were measured from trees at two forested sites that have been impacted differently by the mountain pine beetle (MPB), with one having higher mortality and the other with lower mortality. Differences in the amounts and chemical diversity of BVOC between the two sites and from apparently healthy trees versus trees in different stages of MPB attack are presented, as well as (for one site) observed seasonal variability in emissions. A brief comparison is made of geological and climatic characteristics as well as prior disturbances (both natural and man-made) at each site. Trees sampled at the site experiencing high MPB-related tree mortality had lower chemodiversity in terms of monoterpene (MT) emission profiles, while profiles were more diverse at the lower-mortality site. Also at the higher-mortality site, MPB-infested trees in various stages of decline had lower emissions of sesquiterpenes (SQTs) compared to healthy trees, while at the site with lower mortality, MPB-survivors had significantly higher SQT emissions during part of the growing season when compared to both uninfested and newly infested trees. SQT profiles differed between the two sites and, like monoterpene and oxygenated VOC profiles, varied through the season. For the low-mortality site in which repeated measurements were made over the course of the early summer–late fall, higher chemical diversity was observed in early- compared to late-season measurements for all compound classes investigated (MT, oxygenated VOC, and SQT), with the amount of change appearing to correlate to the MPB status of the trees studied. Emissions of 2-methyl-3-buten-2-ol (MBO) had a distinct seasonal signal but were not much different between healthy or infested trees, except in trees with dead needles, from which emissions of this compound were negligible, and in late-season MPB survivors, in which they were higher than in newly infested or uninfested trees. Emissions of SQT were significantly higher in the MPB survivors during both mid- and late-season sampling at the low-mortality site. The changes in emissions could have implications for regional air quality and climate through changes in ozone and aerosol distributions, although this study was designed as a preliminary screening effort and not enough individuals were sampled for all of the observed differences to be statistically demonstrated. Despite this, the compelling differences in emissions observed between the sites and individual trees with differing MPB-infestation statuses and the potential impacts these have on regional atmospheric chemistry argue for further research in this topic.
Dissertations / Theses on the topic "Tropospheric ozone, climate change, forest, BVOC emission"
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CARRIERO, GIULIA. "Ozone and climate change impacts on forest ecosystems." Doctoral thesis, 2016. http://hdl.handle.net/2158/1027850.
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The increase of tropospheric ozone pollution is affecting forest ecosystems as climate change. This thesis reports the interactions of plant responses to ozone and soil nutrients considering implications for future climate change. The study focuses on mechanisms of action of: ozone pollution on tree functionality and ozone and soil nutrients on BVOC emitted by vegetation