15 research outputs found

    Impact of Subglacial Freshwater Discharge on Pine Island Ice Shelf

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    Satellite-based estimates of ice shelf melt rates reach similar to 200 m yr-1 close to the grounding line of Pine Island Glacier, in West Antarctica. However, ocean simulations have not yet been able to reproduce such high melt rates, even with high-resolution models. Here, we use a regional model of Pine Island ice shelf cavity and study the impact of subglacial freshwater discharge on simulated ice shelf melt rates and ocean circulation in the cavity. We show that subglacial freshwater discharge substantially enhances ice shelf melting close to the grounding line, successfully simulating high ice shelf melt rates suggested by observations. The buoyant mixture of glacial meltwater plume rises to similar to 27.4 isopycnal surfaces, following topographically constrained current, and spreads into mid-depths at the ice shelf front. The role of freshwater discharge is likely to remain unchanged over the coming decades given the projected evolution of runoff and rainfall over Pine Island basin

    Undercutting of marine‐terminating glaciers in West Greenland

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    Marine-terminating glaciers control most of Greenland's ice discharge into the ocean, but little is known about the geometry of their frontal regions. Here we use side-looking, multibeam echo sounding observations to reveal that their frontal ice cliffs are grounded deeper below sea level than previously measured and their ice faces are neither vertical nor smooth but often undercut by the ocean and rough. Deep glacier grounding enables contact with subsurface, warm, salty Atlantic waters (AW) which melts ice at rates of meters per day. We detect cavities undercutting the base of the calving faces at the sites of subglacial water (SGW) discharge predicted by a hydrological model. The observed pattern of undercutting is consistent with numerical simulations of ice melt in which buoyant plumes of SGW transport warm AW to the ice faces. Glacier undercutting likely enhances iceberg calving, impacting ice front stability and, in turn, the glacier mass balance

    Formation, ageing and thermal properties of secondary organic aerosol

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    In order to properly represent and predict the effects of aerosol in climate systems, an accurate description of their formation and properties is needed. This thesis describes work done to increase the knowledge of processes and properties of atmospherically relevant secondary organic aerosol (SOA) from both biogenic and anthropogenic origin. The common theme for these projects is the use of a Volatility Tandem Differential Mobility Analyser (VTDMA) setup, which in combination with other observations has generated insight into both detailed chemical mechanisms and physical processes that eventually could be suitable for testing in air quality or climate models. During the course of this work, the experimental facility the Gothenburg Flow Reactor for Oxidation Studies at low Temperatures (G-FROST) and the VTDMA setup, as well as a corresponding data evaluation methodology, have been improved and refined. Thermal properties could be linked to both formation and ageing processes of SOA. Using a VTDMA setup, where the thermal characteristics of SOA were measured at a range of evaporation temperatures, a sigmoidal fit to the data enabled parameterisation of their volatility properties. The parameters extracted were e.g. the temperature corresponding to a volume fraction remaining of 0.5 (TVFR0.5) and the slope factor (SVFR), which are measures of the general volatility and the volatility distribution of the condensed phase products, respectively. A higher TVFR0.5 indicates lower volatility, while an increase of SVFR states a broader distribution of vapour pressures. The response of these parameters from changes in experimental conditions could be linked to processes occurring both in the gaseous and the condensed phase. In photo-chemical experiments, the change in TVFR0.5 and SVFR could be described using the OH dose. The gas phase processes were found to be very important for SOA ageing, driven mainly by OH radical exposure in the outdoor chamber SAPHIR. However, processes in the condensed phase, such as plausible non oxidative ageing processes and non-liquid behaviour of SOA particles, were also observed. Detailed studies of ozonolysis of the boreal forest monoterpenes β-pinene and limonene were enabled by precise control of reaction conditions using the G-FROST. The experimental findings in response to e.g. water and radical conditions emphasized the difference in ozonolysis reaction paths between endo- and exocyclic compounds. The results support the recently suggested decomposition of the stabilized Criegee Intermediate via the hydroperoxide channel in ozonolysis of β-pinene

    Tracking PM2.5 and O3 Pollution and the Related Health Burden in China 20132020

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    Based on the exposure data sets from the Tracking Air Pollution in China (TAP, http://tapdata.org.cn/), we characterized the spatiotemporal variations in PM2.5 and O3 exposures and quantified the long- and short-term exposure related premature deaths during 2013–2020 with respect to the two-stage clean air actions (2013–2017 and 2018–2020). We find a 48% decrease in national PM2.5 exposure during 2013–2020, although the decrease rate has slowed after 2017. At the same time, O3 pollution worsened, with the average April–September O3 exposure increased by 17%. The improved air quality led to 308 thousand and 16 thousand avoided long- and short-term exposure related deaths, respectively, in 2020 compared to the 2013 level, which was majorly attributed to the reduction in ambient PM2.5 concentration. It is also noticed that with smaller PM2.5 reduction, the avoided long-term exposure associated deaths in 2017–2020 (13%) was greater than that in 2013–2017 (9%), because the exposure–response curve is nonlinear. As a result of the efforts in reducing PM2.5-polluted days with the daily average PM2.5 higher than 75 μg/m3 and the considerable increase in O3-polluted days with the daily maximum 8 h average O3 higher than 160 μg/m3, deaths attributable to the short-term O3 exposure were greater than those due to PM2.5 exposure since 2018. Future air quality improvement strategies for the coordinated control of PM2.5 and O3 are urgently needed

    Influence of Ozone and Radical Chemistry on Limonene Organic Aerosol Production and Thermal Characteristics

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    Limonene has a strong tendency to form secondary organic aerosol (SOA) in the atmosphere and in indoor environments. Initial oxidation occurs mainly via ozone or OH radical chemistry. We studied the effect of O3 concentrations with or without a OH radical scavenger (2-butanol) on the SOA mass and thermal characteristics using the Gothenburg Flow Reactor for Oxidation Studies at Low Temperatures and a volatility tandem differential mobility analyzer. The SOA mass using 15 ppb limonene was strongly dependent on O3 concentrations and the presence of a scavenger. The SOA volatility in the presence of a scavenger decreased with increasing levels of O3, whereas without a scavenger, there was no significant change. A chemical kinetic model was developed to simulate the observations using vapor pressure estimates for compounds that potentially contributed to SOA. The model showed that the product distribution was affected by changes in both OH and ozone concentrations, which partly explained the observed changes in volatility, but was strongly dependent on accurate vapor pressure estimation methods. The model–experiment comparison indicated a need to consider organic peroxides as important SOA constituents. The experimental findings could be explained by secondary condensed-phase ozone chemistry, which competes with OH radicals for the oxidation of primary unsaturated products
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