Browsing by Author "Robinson, Andrew D."
Now showing 1 - 5 of 5
Results Per Page
Sort Options
Item Open Access Atmospheric isoprene measurements reveal larger-than-expected Southern Ocean emissions(Springer Nature, 2024-03-22) Ferracci, Valerio; Weber, James; Bolas, Conor G.; Robinson, Andrew D.; Tummon, Fiona; Rodríguez-Ros, Pablo; Cortés-Greus, Pau; Baccarini, Andrea; Jones, Roderic L.; Galí, Martí; Simó, Rafel; Schmale, Julia; Harris, Neil R. P.Isoprene is a key trace component of the atmosphere emitted by vegetation and other organisms. It is highly reactive and can impact atmospheric composition and climate by affecting the greenhouse gases ozone and methane and secondary organic aerosol formation. Marine fluxes are poorly constrained due to the paucity of long-term measurements; this in turn limits our understanding of isoprene cycling in the ocean. Here we present the analysis of isoprene concentrations in the atmosphere measured across the Southern Ocean over 4 months in the summertime. Some of the highest concentrations ( >500 ppt) originated from the marginal ice zone in the Ross and Amundsen seas, indicating the marginal ice zone is a significant source of isoprene at high latitudes. Using the United Kingdom Earth System Model we show that current estimates of sea-to-air isoprene fluxes underestimate observed isoprene by a factor >20. A daytime source of isoprene is required to reconcile models with observations. The model presented here suggests such an increase in isoprene emissions would lead to >8% decrease in the hydroxyl radical in regions of the Southern Ocean, with implications for our understanding of atmospheric oxidation and composition in remote environments, often used as proxies for the pre-industrial atmosphere.Item Open Access Estimating the size of a methane emission point source at different scales: from local to landscape(European Geosciences Union (EGU) / Copernicus Publications, 2017-06-29) Riddick, Stuart N.; Connors, Sarah; Robinson, Andrew D.; Manning, Alistair J.; Jones, Pippa S. D.; Lowry, David; Nisbet, Euan; Skelton, Robert L.; Allen, Grant; Pitt, Joseph; Harris, Neil R. P.High methane (CH4) mixing ratios (up to 4 ppm) have occurred sporadically at our measurement site in Haddenham, Cambridgeshire, since July 2012. Isotopic measurements and back trajectories show that the source is the Waterbeach Waste Management Park 7 km SE of Haddenham. To investigate this further, measurements were made on 30 June and 1 July 2015 at other locations nearer to the source. Landfill emissions have been estimated using three different approaches at different scales; near source using the WindTrax inversion dispersion model, middle distance using a Gaussian plume (GP) model and at the landscape scale using the Numerical Atmospheric Modelling Environment (NAME) Inversion Technique for Emission Modelling (InTEM) inversion. The emission estimates derived using the WindTrax and Gaussian plume (GP) approaches agree well for the period of intense observations. Applying the Gaussian plume approach to all periods of elevated measurements seen at Haddenham produces year-round and monthly landfill emission estimates with an estimated annual emission of 11.6 GgCH(4) yr(-1). The monthly emission estimates are highest in winter (2160 kg h(-1) in February) and lowest in summer (620 kg h(-1) in July). These data identify the effects of environmental conditions on landfill CH4 production and highlight the importance of year-round measurements to capture seasonal variability in CH4 emission.Item Open Access Estimating the size of a methane emission point-source at different scales: from local to landscape(Copernicus Publications, 2016-11-22) Riddick, Stuart N.; Connors, Sarah; Robinson, Andrew D.; Manning, Alistair J.; Jones, Pippa S. D.; Lowry, David; Nisbet, Euan; Skelton, Robert L.; Allen, Grant; Pitt, Joseph; Harris, Neil R. P.High methane (CH4) mixing ratios (up to 4 ppm) have occurred sporadically at our measurement site in Haddenham, Cambridgeshire since July 2012. Isotopic measurements and back trajectories show that the source is the Waterbeach Waste management park 7 km SE of Haddenham. To investigate this further, measurements were made on June 30th and July 1st 2015 at other locations nearer to the source. Landfill emissions have been estimated using three different approaches (WindTrax, Gaussian plume, and NAME InTEM inversion) applied to the measurements made close to source and at Haddenham. The emission estimates derived using the WindTrax and Gaussian plume approaches agree well for the period of intense observations. Applying the Gaussian plume approach to all periods of elevated measurements seen at Haddenham produces year-round and monthly landfill emission estimates. The estimated annual emissions vary between 11.6 and 13.7 Gg CH4 yr−1. The monthly emission estimates are highest in winter (2160 kg hr−1 in February) and lowest in summer (620 kg hr−1 in July). These data identify the effects of environmental conditions on landfill CH4 production and highlight the importance of year-round measurement to capture seasonal variability in CH4 emission. We suggest the landscape inverse modelling approach described in this paper is in good agreement with more labour-intensive near-source approaches and can be used to identify point-sources within an emission landscape to provide high-quality emission estimates.Item Open Access iDirac: a field-portable instrument for long-term autonomous measurements of isoprene and selected VOCs(European Geosciences Union, 2020-02-19) Bolas, Conor G.; Ferracci, Valerio; Robinson, Andrew D.; Mead, Mohammed Iqbal; Nadzir, Mohd Shahrul Mohd; Pyle, John A.; Jones, Roderic L.; Harris, Neil R. P.The iDirac is a new instrument to measure selected hydrocarbons in the remote atmosphere. A robust design is central to its specifications, with portability, power efficiency, low gas consumption and autonomy as the other driving factors in the instrument development. The iDirac is a dual-column isothermal oven gas chromatograph with photoionisation detection (GC-PID). The instrument is designed and built in-house. It features a modular design, with the novel use of open-source technology for accurate instrument control. Currently configured to measure biogenic isoprene, the system is suitable for a range of compounds. For isoprene measurements in the field, the instrument precision (relative standard deviation) is ±10 %, with a limit of detection down to 38 pmol mol−1 (or ppt). The instrument was first tested in the field in 2015 during a ground-based campaign, and has since shown itself suitable for deployment in a variety of environments and platforms. This paper describes the instrument design, operation and performance based on laboratory tests in a controlled environment as well as during deployments in forests in Malaysian Borneo and central England.Item Open Access Seasonal and long term variations of surface ozone concentrations in Malaysian Borneo(Elsevier, 2016-08-27) Latif, Mohd Talib; Dominick, Doreena; Ahamad, Fatimah; Ahamad, Nur Shuhada; Khan, Md Firoz; Juneng, Liew; Xiang, Chung Jing; Nadzir, Mohd Shahrul Mohd; Robinson, Andrew D.; Ismail, Marzuki; Mead, Mohammed Iqbal; Harris, Neil R. P.Malaysian Borneo has a lower population density and is an area known for its lush rainforests. However, changes in pollutant profiles are expected due to increasing urbanisation and commercial-industrial activities. This study aims to determine the variation of surface {O3} concentration recorded at seven selected stations in Malaysian Borneo. Hourly surface {O3} data covering the period 2002 to 2013, obtained from the Malaysian Department of Environment (DOE), were analysed using statistical methods. The results show that the concentrations of {O3} recorded in Malaysian Borneo during the study period were below the maximum Malaysian Air Quality Standard of 100 ppbv. The hourly average and maximum {O3} concentrations of 31 and 92 ppbv reported at Bintulu (S3) respectively were the highest among the {O3} concentrations recorded at the sampling stations. Further investigation on {O3} precursors show that sampling sites located near to local petrochemical industrial activities, such as Bintulu (S3) and Miri (S4), have higher NO2/NO ratios (between 3.21 and 5.67) compared to other stations. The normalised {O3} values recorded at all stations were higher during the weekend compared to weekdays (unlike its precursors) which suggests the influence of {O3} titration by {NO} during weekdays. The results also show that there are distinct seasonal variations in {O3} across Borneo. High surface {O3} concentrations were usually observed between August and September at all stations with the exception of station {S7} on the east coast. Majority of the stations (except {S1} and S6) have recorded increasing averaged maximum concentrations of surface {O3} over the analysed years. Increasing trends of {NO2} and decreasing trends of {NO} influence the yearly averaged maximum of {O3} especially at S3. This study also shows that variations of meteorological factors such as wind speed and direction, humidity and temperature influence the concentration of surface O3.