Found 9849 publications. Showing page 285 of 394:
Coordinated numerical ensemble experiments with six different state-of-the-art atmosphere models have been used in order to evaluate the respective impact of the observed Arctic sea ice and sea surface temperature (SST) variations on air temperature variations in mid and high latitude land areas. Two sets of experiments have been designed; in the first set (EXP1), observed daily sea ice concentration and SST variations are used as lower boundary forcing over 1982–2014 while in the second set (EXP2) the SST variations are replaced by the daily SST climatology. The observed winter 2 m air temperature (T2m) variations are relatively well reproduced in a number of mid and high latitude land areas in EXP1, with best agreement in southwestern North America and northern Europe. Sea ice variations are important for the interannual T2m variations in northern Europe but have limited impact on all other mid and high latitude land regions. In particular, sea ice variations do not contribute to the observed opposite variations in the Arctic and mid latitude in our model experiments. The spread across ensemble members is large and many ensemble members are required to reproduce the observed T2m variations over northern Europe in our models. The amplitude of T2m anomalies in the coldest observed winters over northern Europe is not reproduced by our multi-model ensemble means. However, the sea ice conditions in these respective winters and mainly the thermodynamic response to the ice anomalies lead to an enhanced likelihood for occurrence of colder than normal winters and extremely cold winters. Still, the main reason for the observed extreme cold winters is internal atmospheric dynamics. The coldest simulated northern European winters in EXP1 and EXP2 between 1982 and 2014 show the same large scale T2m and atmospheric circulation anomaly patterns as the observed coldest winters, indicating that the models are well able to reproduce the processes, which cause these cold anomalies. The results are robust across all six models used in this study.
Springer
2018
Low concentrations of persistent organic pollutants (POPs) in air at Cape Verde
Ambient air is a core medium for monitoring of persistent organic pollutants (POPs) under the Stockholm Convention
and is used in studies of global transports of POPs and their atmospheric sources and source regions. Still,
data based on active air sampling remain scarce in many regions. The primary objectives of this study were to
(i) monitor concentrations of selected POPs in air outside West Africa, and (ii) to evaluate potential atmospheric
processes and source regions affecting measured concentrations. For this purpose, an active high-volume air
sampler was installed on the Cape Verde Atmospheric Observatory at Cape Verde outside the coast of West
Africa. Sampling commenced in May 2012 and 43 samples (24 h sampling) were collected until June 2013. The samples were analyzed for selected polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), hexachlorobenzene (HCB) and chlordanes. The concentrations of these POPs at Cape Verde were generally low and comparable to remote sites in the Arctic for several compounds. Seasonal trends varied between compounds and concentrations exhibited strong temperature dependence for chlordanes. Our results indicate
net volatilization fromthe Atlantic Ocean north of Cape Verde as sources of these POPs. Air mass back trajectories
demonstrated that air masses measured at Cape Verdewere generally transported fromthe Atlantic Ocean or the North African continent. Overall, the low concentrations in air at Cape Verde were likely explained by absence of major emissions in areas from which the air masses originated combined with depletion during long-range atmospheric
transport due to enhanced degradation under tropical conditions (high temperatures and concentrations of hydroxyl radicals).
Elsevier
2018
2018
Seasonality of aerosol optical properties in the Arctic
Given the sensitivity of the Arctic climate to short-lived climate forcers, long-term in situ surface measurements of aerosol parameters are useful in gaining insight into the magnitude and variability of these climate forcings. Seasonality of aerosol optical properties – including the aerosol light-scattering coefficient, absorption coefficient, single-scattering albedo, scattering Ångström exponent, and asymmetry parameter – are presented for six monitoring sites throughout the Arctic: Alert, Canada; Barrow, USA; Pallas, Finland; Summit, Greenland; Tiksi, Russia; and Zeppelin Mountain, Ny-Ålesund, Svalbard, Norway. Results show annual variability in all parameters, though the seasonality of each aerosol optical property varies from site to site. There is a large diversity in magnitude and variability of scattering coefficient at all sites, reflecting differences in aerosol source, transport, and removal at different locations throughout the Arctic. Of the Arctic sites, the highest annual mean scattering coefficient is measured at Tiksi (12.47Mm−1), and the lowest annual mean scattering coefficient is measured at Summit (1.74Mm−1). At most sites, aerosol absorption peaks in the winter and spring, and has a minimum throughout the Arctic in the summer, indicative of the Arctic haze phenomenon; however, nuanced variations in seasonalities suggest that this phenomenon is not identically observed in all regions of the Arctic. The highest annual mean absorption coefficient is measured at Pallas (0.48Mm−1), and Summit has the lowest annual mean absorption coefficient (0.12Mm−1). At the Arctic monitoring stations analyzed here, mean annual single-scattering albedo ranges from 0.909 (at Pallas) to 0.960 (at Barrow), the mean annual scattering Ångström exponent ranges from 1.04 (at Barrow) to 1.80 (at Summit), and the mean asymmetry parameter ranges from 0.57 (at Alert) to 0.75 (at Summit). Systematic variability of aerosol optical properties in the Arctic supports the notion that the sites presented here measure a variety of aerosol populations, which also experience different removal mechanisms. A robust conclusion from the seasonal cycles presented is that the Arctic cannot be treated as one common and uniform environment but rather is a region with ample spatiotemporal variability in aerosols. This notion is important in considering the design or aerosol monitoring networks in the region and is important for informing climate models to better represent short-lived aerosol climate forcers in order to yield more accurate climate predictions for the Arctic.
2018
2018
2018
2018
This study quantifies the present-day global and regional distributions (2010–2014) and trends (2000–2014) for five ozone metrics relevant for short-term and long-term human exposure. These metrics, calculated by the Tropospheric Ozone Assessment Report, are: 4th highest daily maximum 8-hour ozone (4MDA8); number of days with MDA8 > 70 ppb (NDGT70), SOMO35 (annual Sum of Ozone Means Over 35 ppb) and two seasonally averaged metrics (3MMDA1; AVGMDA8). These metrics were explored at ozone monitoring sites worldwide, which were classified as urban or non-urban based on population and nighttime lights data.
Present-day distributions of 4MDA8 and NDGT70, determined predominantly by peak values, are similar with highest levels in western North America, southern Europe and East Asia. For the other three metrics, distributions are similar with North–South gradients more prominent across Europe and Japan. Between 2000 and 2014, significant negative trends in 4MDA8 and NDGT70 occur at most US and some European sites. In contrast, significant positive trends are found at many sites in South Korea and Hong Kong, with mixed trends across Japan. The other three metrics have similar, negative trends for many non-urban North American and some European and Japanese sites, and positive trends across much of East Asia. Globally, metrics at many sites exhibit non-significant trends. At 59% of all sites there is a common direction and significance in the trend across all five metrics, whilst 4MDA8 and NDGT70 have a common trend at ~80% of all sites. Sensitivity analysis shows AVGMDA8 trends differ with averaging period (warm season or annual). Trends are unchanged at many sites when a 1995–2014 period is used; although fewer sites exhibit non-significant trends. Over the longer period 1970–2014, most Japanese sites exhibit positive 4MDA8/SOMO35 trends. Insufficient data exist to characterize ozone trends for the rest of Asia and other world regions.
2018
2018
2018
2018
Tiltaksutredning for lokal luftkvalitet i Sarpsborg og Fredrikstad
Tiltaksutredningen omfatter en kartlegging av luftkvaliteten i Fredrikstad og Sarpsborg ved trafikkberegninger og utslipps- ogspredningsberegninger for PM10 og NO2 for dagens situasjon (2016) og framtidig situasjon (2022). Forurensningsnivåene er innenfor de juridiske grenseverdiene og det er ikke formelt krav til tiltak utover gjeldende handlingsplan (2017). For å redusere risikoen for overskridelser av grenseverdiene i et «ekstrem år» og generelt forbedre luftkvaliteten, er enkelte nye tiltak effektberegnet sammen med tiltak i Bypakke Nedre Glomma. Basert på resultatene fra beregningene og i samarbeid
med oppdragsgiver og prosjektgruppen, er det foreslått en revidert seks-punkts handlingsplan, med ytterligere tre tiltak for forbedret luftkvalitet utover de juridiske kravene. Tiltaksutredningen med handlingsplan skal behandles politisk.
NILU
2018
ThermoFisher Scientific
2018
2018
In the frame of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx), we analyse the budget of primary aerosols and secondary inorganic aerosols over the Mediterranean Basin during the years 2012 and 2013. To do this, we use two year-long numerical simulations with the chemistry-transport model MOCAGE validated against satellite- and ground-based measurements. The budget is presented on an annual and a monthly basis on a domain covering 29 to 47° N latitude and 10° W to 38° E longitude.
The years 2012 and 2013 show similar seasonal variations. The desert dust is the main contributor to the annual aerosol burden in the Mediterranean region with a peak in spring, and sea salt being the second most important contributor. The secondary inorganic aerosols, taken as a whole, contribute a similar level to sea salt. The results show that all of the considered aerosol types, except for sea salt aerosols, experience net export out of our Mediterranean Basin model domain, and thus this area should be considered as a source region for aerosols globally. Our study showed that 11 % of the desert dust, 22.8 to 39.5 % of the carbonaceous aerosols, 35 % of the sulfate and 9 % of the ammonium emitted or produced into the study domain are exported. The main sources of variability for aerosols between 2012 and 2013 are weather-related variations, acting on emissions processes, and the episodic import of aerosols from North American fires.
In order to assess the importance of the anthropogenic emissions of the marine and the coastal areas which are central for the economy of the Mediterranean Basin, we made a sensitivity test simulation. This simulation is similar to the reference simulation but with the removal of the international shipping emissions and the anthropogenic emissions over a 50 km wide band inland along the coast. We showed that around 30 % of the emissions of carbonaceous aerosols and 35 to 60 % of the exported carbonaceous aerosols originates from the marine and coastal areas. The formation of 23, 27 and 27 %, respectively of, ammonium, nitrate and sulfate aerosols is due to the emissions within the marine and coastal area.
2018
2018