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This report has been prepared by the SETAC Europe Scientific Task Group on Global And RegionaL Impact Categories (SETAC-Europe/STG-GARLIC) that is installed by the 2nd SETAC Europe working group on life cycle impact assessment (WIA-2). This document is background to a chapter written by the same authors under the title “Climate change, stratospheric ozone depletion, photo-oxidant formation, acidification and eutrophication” in Udo de Haes et al. (2002). The chapter summarises the work of the STG-GARLIC and aims to give a state-of-the-art review of the best available practice(s) regarding category indicators and lists of concomitant characterisation factors for climate change, stratospheric ozone depletion, photo-oxidant formation, acidification, and aquatic and terrestrial eutrophication. Backgrounds on each of the specific impact categories are given in another background report from Klöpffer and Potting (2001).
This background report provides details on a selection of general issues relevant in relation to LCA and characterisation of impact in LCA. The document starts with a short introduction of the LCA methodology and impact assessment in LCA for non LCA-experts. LCA experts, on the other hand, will usually not be familiar in-depth with scientific and political backgrounds of the specific impact categories. A review of this is given. Also the discussion is provided about the issue of the position of the category indicator in the causality chain, and into the related issue of spatial differentiation. These two issues appeared to be one of the core items for SETAC-Europe/STG-GARLIC.
Messkampagnen im Projekt METPVNET zur Verbesserung der PV- Erzeugungsprognose auf Verteilnetzebene
(2018)
An aircraft plume model has been developed on the basis of two coupled trajectory box models. Two boxes, one for plume and one for background conditions, are coupled by means of a mixing parameterization based on turbulence theory. The model considers comprehensive gas phase chemistry for the tropopause region including acetone, ethane and their oxidation products. Heterogeneous halogen, N2O5 and HOx chemistry on various types of background and aircraft-induced aerosols (liquid and ice) is considered, using state-of-the-art solubility dependent uptake coefficients for liquid phase reactions. The microphysical scheme allows for coagulation, gas-diffusive particle growth and evaporation, so that the particle development from 1s after emission to several days can be simulated. Model results are shown, studying emissions into the upper troposphere as well as into the lowermost stratosphere for contrail and non-contrail conditions. We show the microphysical and chemical evolution of spreading plumes and use the concept of mean plume encounter time, tl, to define effective emission and perturbation indices (EEIs and EPIs) for the North Atlantic Flight Corridor (NAFC) showing EEI(NOy) and EPI(O3) for various background conditions, such as relative humidity, local time of emission, and seasonal variations. Our results show a high sensitivity of EEI and EPIs on the exact conditions under which emissions take place. The difference of EEIs with and without considering plume processes indicates that these processes cannot be neglected.
Nitric acid partitioning in cirrus clouds: a synopsis based on field, laboratory and model studies
(2003)
From a synopsis of field, laboratory and model studies at T>205 K as well as from the field experiments POLSTAR at T<205 K we derive a general picture of the partitioning of nitric acid (HNO3) in cirrus clouds and a new hypothesis on the uptake of HNO3 on ice particles:
A substantial part of nitric acid remains in the gas phase under cirrus cloud conditions. The HNO3 removed from the gas phase is distributed between interstitial aerosol and ice particles in dependence on the temperature and ice surface, respectively. In cold cirrus clouds with small ice surface areas (T <205 K) the partitioning is strongly in favour of interstitial ternary solution particles while in warmer cirrus clouds with large ice surface areas the uptake on ice dominates. Consequently, denitrification via sedimenting ice particles may occur only in the -more frequently occurring- warm cirrus clouds
The HNO3 coverage on ice is found to be different for ice particles and ice films. On ice films the coverage can increase with decreasing temperature from about 0.1 to 0.8 monolayer, while that on ice particles is found to decrease with temperature and PHNO3 from 0.1 to 0.001 monolayer. An HNO3 uptake behaviour following dissociative Langmuir isotherms where the coverage decreases for descending temperatures may explain the observations for ice particles
From a comparison of the HNO3 measurements with model calculations it is found that (i) the global model of Lawrence and Crutzen (1998) overestimates the HNO3 partitioning in favour of the ice particles (ii) the Langmuir surface chemistry model of Tabazadeh et al. (1999) overestimates HNO3 coverages for temperatures ≤210 K More appropriate coverages are calculated when implementing in that model a temperature dependent function for the adsorption free energy (ΔGads (T)), which is empirically derived from the coverage measurements.
For the winter 1999/2000 transport of air masses out of the vortex to mid-latitudes and ozone destruction inside and outside the northern polar vortex is studied to quantify the impact of earlier winter (before March) polar ozone destruction on mid-latitude ozone.
Nearly 112 000 trajectories are started on 1 December 1999 on 6 different potential temperature levels between 500–600 K and for a subset of these trajectories photo-chemical box-model calculations are performed. We linked a decline of −0.9% of mid-latitude ozone in this layer occurring in January and February 2000 to ozone destruction inside the vortex and successive transport of these air masses to mid-latitudes.
Further, the impact of denitrification, PSC-occurrence and anthropogenic chlorine loading on future stratospheric ozone is determined by applying various scenarios. Lower stratospheric temperatures and denitrification were found to play the most important role in the future evolution of polar ozone depletion.
We examine the effect of nanometer-sized aircraft-induced aqueous sulfuric acid (H2SO4/H2O) particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density due to air traffic in the North Atlantic Flight Corridor (NAFC) and a chemical box model. We confirm large scale model results that at temperatures T>210 K additional ozone loss -- mainly caused by hydrolysis of BrONO2 and N2O5 -- scales in proportion with the aviation-produced increase of the background aerosol surface area. However, at lower temperatures (< 210 K) we isolate two effects which efficiently reduce the aircraft-induced perturbation: (1) background particles growth due to H2O and HNO3 uptake enhance scavenging losses of aviation-produced liquid particles and (2) the Kelvin effect efficiently limits chlorine activation on the small aircraft-induced droplets by reducing the solubility of chemically reacting species. These two effects lead to a substantial reduction of heterogeneous chemistry on aircraft-induced volatile aerosols under cold conditions. In contrast we find contrail ice particles to be potentially important for heterogeneous chlorine activation and reductions in ozone levels. These features have not been taken into consideration in previous global studies of the atmospheric impact of aviation. Therefore, to parameterize them in global chemistry and transport models, we propose the following parameterisation: scale the hydrolysis reactions by the aircraft-induced surface area increase, and neglect heterogeneous chlorine reactions on liquid plume particles but not on ice contrails and aircraft induced ice clouds.