Chiara Di Marco
Natural Environment Research Council
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Philosophical Transactions of the Royal Society B | 2011
D. Fowler; E. Nemitz; Pawel K. Misztal; Chiara Di Marco; U. Skiba; James Ryder; Carole Helfter; J. Neil Cape; Susan M. Owen; J. R. Dorsey; Martin Gallagher; Mhairi Coyle; Gavin Phillips; Brian Davison; Ben Langford; Rob MacKenzie; Jennifer Muller; Jambery Siong; Cesare Dari-Salisburgo; Piero Di Carlo; Eleonora Aruffo; Franco Giammaria; J. A. Pyle; C. Nicholas Hewitt
This paper reports measurements of land–atmosphere fluxes of sensible and latent heat, momentum, CO2, volatile organic compounds (VOCs), NO, NO2, N2O and O3 over a 30 m high rainforest canopy and a 12 m high oil palm plantation in the same region of Sabah in Borneo between April and July 2008. The daytime maximum CO2 flux to the two canopies differs by approximately a factor of 2, 1200 mg C m−2 h−1 for the oil palm and 700 mg C m−2 h−1 for the rainforest, with the oil palm plantation showing a substantially greater quantum efficiency. Total VOC emissions are also larger over the oil palm than over the rainforest by a factor of 3. Emissions of isoprene from the oil palm canopy represented 80 per cent of the VOC emissions and exceeded those over the rainforest in similar light and temperature conditions by on average a factor of 5. Substantial emissions of estragole (1-allyl-4-methoxybenzene) from the oil palm plantation were detected and no trace of this VOC was detected in or above the rainforest. Deposition velocities for O3 to the rainforest were a factor of 2 larger than over oil palm. Emissions of nitrous oxide were larger from the soils of the oil palm plantation than from the soils of the rainforest by approximately 25 per cent. It is clear from the measurements that the large change in the species composition generated by replacing rainforest with oil palm leads to profound changes in the net exchange of most of the trace gases measured, and thus on the chemical composition of the boundary layer over these surfaces.
Archive | 2009
Massimo Vieno; Anthony J. Dore; Peter Wind; Chiara Di Marco; E. Nemitz; Gavin Phillips; Leonor Tarrason; Mark A. Sutton
The EMEP Unified model (Simpson et al. 2003; http://www.emep.int) is an Eulerian model that is driven by real-time meteorology. The model is applied over Europe for multiple years on a 50 × 50 km grid, with meteorological fields updated every 3 h. While comparisons with measurements have shown generally robust performance of the EMEP model on a European scale (e.g. Simpson et al. 2006), pollutants such as reactive nitrogen and sulphur have a high spatial variability in their emissions and a short life time. Therefore, the associated dry deposition also has a high spatial variability (Vieno 2006; van Pul et al. 2009, this volume). This is very important when critical loads of nitrogen are calculated for specific ecosystems. For this reason a number of models have been developed for high resolution operation at a national scale. To address these issues for the UK, the EMEP Unified Model is being developed, using a nested approach. This model application, referred to as EMEP4UK, has been developed at a 5 × 5 km resolution covering the whole of the British Isles. By comparison with existing statistical models of atmospheric chemistry and transport over the UK (e.g. Singles et al. 1998; Lee et al. 2000; Metcalfe et al. 2001; Fournier et al. 2005; Vieno 2006; Dore et al. 2007), the EMEP4UK model therefore has the advantage of using real time meteorology, enabling the interactions between emissions, meteorology, concentrations and deposition to be addressed at a fine spatial scale.
Atmospheric Chemistry and Physics | 2017
Silvia Bucci; Paolo Cristofanelli; Stefano Decesari; Angela Marinoni; S. Sandrini; Johannes Größ; Alfred Wiedensohler; Chiara Di Marco; E. Nemitz; F. Cairo; Luca Di Liberto; Federico Fierli
Studying the vertical distribution of aerosol particle physical and chemical properties in the troposphere is essential to understand the relative importance of local emission processes vs. long-range transport for column-integrated aerosol properties (e.g. the aerosol optical depth, AOD, affecting regional climate) as well as for the aerosol burden and its impacts on air quality at the ground. The main objective of this paper is to investigate the transport of desert dust in the middle troposphere and its intrusion into the planetary boundary layer (PBL) over the Po Valley (Italy), a region considered one of the greatest European pollution hotspots for the frequency that particulate matter (PM) limit values are exceeded. Events of mineral aerosol uplift from local (soil) sources and phenomena of hygroscopic growth at the ground are also investigated, possibly affecting the PM concentration in the region as well. During the PEGASOS 2012 field campaign, an integrated observing–modelling system was set up based on near-surface measurements (particle concentration and chemistry), vertical profiling (backscatter coefficient profiles from lidar and radiosoundings) and Lagrangian air mass transport simulations by FLEXPART model. Measurements were taken at the San Pietro Capofiume supersite (4439 N, 1137 E; 11 m a.s.l.), located in a rural area relatively close to some major urban and industrial emissive areas in the Po Valley. Mt. Cimone (4412 N, 1042 E; 2165 m a.s.l.) WMO/GAW station observations are also included in the study to characterize regional-scale variability. Results show that, in the Po Valley, aerosol is detected mainly below 2000 m a.s.l. with a prevalent occurrence of non-depolarizing particles (> 50 % throughout the campaign) and a vertical distribution modulated by the PBL daily evolution. Two intense events of mineral dust transport from northern Africa (19–21 and 29 June to 2 July) are observed, with layers advected mainly above 2000 m, but subsequently sinking and mixing in the PBL. As a consequence, a non-negligible occurrence of mineral dust is observed close to the ground (∼ 7 % of occurrence during a 1-month campaign). The observations unambiguously show Saharan dust layers intruding the Po Valley mixing layer and directly affecting the aerosol concentrations near the surface. Finally, lidar observations also indicate strong variability in aerosol on shorter timescales (hourly). Firstly, these highlight events of hygroscopic growth of anthropogenic aerosol, visible as shallow layers of low depolarization near the ground. Such events are identified during early morning hours at high relative humidity (RH) conditions (RH> 80 %). The process is observed concurrently with high PM1 nitrate concentration (up to 15 μg cm−3) and hence mainly explicable by deliquescence of fine anthropogenic particles, and during mineral dust intrusion episodes, when water condensation on dust particles could instead represent the dominant contribution. Secondly, lidar images show frequent events (mean daily occurrence of ∼ 22 % during the whole campaign) of rapid uplift of mineral depolarizing particles in afternoon– evening hours up to 2000 m a.s.l. height. The origin of such particles cannot be directly related to long-range transport Published by Copernicus Publications on behalf of the European Geosciences Union. 5372 S. Bucci et al.: Aerosol particle optical properties in the Po Valley events, being instead likely linked to processes of soil particle resuspension from agricultural lands.
Agricultural and Forest Meteorology | 2010
D. Famulari; E. Nemitz; Chiara Di Marco; Gavin Phillips; R. Thomas; Emily House; D. Fowler
Atmospheric Environment | 2012
Chiara Giorio; Andrea Tapparo; M. Dall'Osto; Roy M. Harrison; David C. S. Beddows; Chiara Di Marco; E. Nemitz
Atmospheric Chemistry and Physics | 2016
Riinu Ots; Dominique E. Young; Massimo Vieno; Lu Xu; Rachel E. Dunmore; J. D. Allan; Hugh Coe; Leah R. Williams; Scott C. Herndon; Nga L. Ng; Jacqueline F. Hamilton; Robert Bergström; Chiara Di Marco; E. Nemitz; Ian A. MacKenzie; Jeroen J. P. Kuenen; David Green; Stefan Reis; Mathew R. Heal
Biogeosciences | 2016
S.K. Jones; Carole Helfter; Margaret Anderson; Mhairi Coyle; Claire Campbell; D. Famulari; Chiara Di Marco; Netty van Dijk; Y. Sim Tang; Cairistiona F.E. Topp; Ralf Kiese; Reimo Kindler; Jan Siemens; Marion Schrumpf; Klaus Kaiser; E. Nemitz; Peter E. Levy; Robert M. Rees; Mark A. Sutton; U. Skiba
Atmospheric Chemistry and Physics | 2016
Riinu Ots; Massimo Vieno; J. D. Allan; Stefan Reis; E. Nemitz; Dominique E. Young; Hugh Coe; Chiara Di Marco; Anais Detournay; Ian A. MacKenzie; David Green; Mathew R. Heal
Archive | 2009
T. Demmers; A. Saponja; E. Nemitz; R. Thomas; Gavin Phillips; Chiara Di Marco; Alan G. McDonald; Jennifer Harris; S. Bennett; S. Stagg; A. Bowry; J. Emery
Archive | 2009
Pawel K. Misztal; Ben Langford; Chiara Di Marco; Gavin Phillips; Nick Hewitt; J. Neil Cape; Mathew R. Heal; E. Nemitz