Found 2533 publications. Showing page 68 of 254:
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
Ny-Ålesund is an international research settlement where the thermodynamics and chemical composition of the air are monitored. The present work investigates the effects of micrometeorological conditions, mesoscale dynamics and local air pollution on the data collected at two different locations around the village. Daily filter measurements of sulphur dioxide and non-sea salt sulphate from the temporary Ny-Ålesund station and permanent Zeppelin mountain station have been analysed along with meteorological data. The influence of different factors representing micrometeorological phenomena and local pollution from ships has been statistically investigated. Seasonal variation of the correlation between the data from Ny-Ålesund and Zeppelin stations is revealed, and the seasonal dependence of the relative contribution of different factors has been analysed. The median concentrations of SO42- measured in Ny-Ålesund increased significantly on days with temperature inversions in winter. In spring, concentrations of SO2 and SO42- were higher than normal at both stations on days with temperature inversions, but lower on days with strong humidity inversions. In summer, local ship traffic affects the SO2 data set from Ny-Ålesund, while no statistically significant influence on the Zeppelin data set has been observed. The pollution from ships has an effect on SO42- values at both stations; however, the concentrations in Ny-Ålesund were higher when local pollution accumulated close to the ground in days with strong humidity inversions.
2018
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
A multi-model comparison of meteorological drivers of surface ozone over Europe
The implementation of European emission abatement strategies has led to a significant reduction in the emissions of ozone precursors during the last decade. Ground-level ozone is also influenced by meteorological factors such as temperature, which exhibit interannual variability and are expected to change in the future. The impacts of climate change on air quality are usually investigated through air-quality models that simulate interactions between emissions, meteorology and chemistry. Within a multi-model assessment, this study aims to better understand how air-quality models represent the relationship between meteorological variables and surface ozone concentrations over Europe. A multiple linear regression (MLR) approach is applied to observed and modelled time series across 10 European regions in springtime and summertime for the period of 2000–2010 for both models and observations. Overall, the air-quality models are in better agreement with observations in summertime than in springtime and particularly in certain regions, such as France, central Europe or eastern Europe, where local meteorological variables show a strong influence on surface ozone concentrations. Larger discrepancies are found for the southern regions, such as the Balkans, the Iberian Peninsula and the Mediterranean basin, especially in springtime. We show that the air-quality models do not properly reproduce the sensitivity of surface ozone to some of the main meteorological drivers, such as maximum temperature, relative humidity and surface solar radiation. Specifically, all air-quality models show more limitations in capturing the strength of the ozone–relative-humidity relationship detected in the observed time series in most of the regions, for both seasons. Here, we speculate that dry-deposition schemes in the air-quality models might play an essential role in capturing this relationship. We further quantify the relationship between ozone and maximum temperature (mo3 − T, climate penalty) in observations and air-quality models. In summertime, most of the air-quality models are able to reproduce the observed climate penalty reasonably well in certain regions such as France, central Europe and northern Italy. However, larger discrepancies are found in springtime, where air-quality models tend to overestimate the magnitude of the observed climate penalty.
2018
This study presents a specifically designed Mercury module in a coupled benthic-pelagic reactive-transport model - Bottom RedOx Model (BROM) that allows to study mercury (Hg) biogeochemistry under different conditions. This module considers the transformation of elemental mercury (Hg(0)), divalent mercury (Hg(II)) and methylmercury (MeHg). The behavior of mercury species in the model is interconnected with changes of oxygen, hydrogen sulfide, iron oxides, organic matter, and biota. We simulated the transformation and transport of Hg species in the water column and upper sediment layer under five different scenarios, combining various levels of oxygenation and trophic state in the Berre lagoon, a shallow eutrophic lagoon of the French Mediterranean coast subjected to seasonal anoxia. The first scenario represents the conditions in the lagoon that are compared with experimental data. The four other scenarios were produced by varying the biological productivity, using low and high nutrient (N and P) concentrations, and by varying the redox conditions using different intensity of vertical mixing in the water column. The results of the simulation show that both oxidized and reduced sediments can accumulate Hg, but any shifts in redox conditions in bottom water and upper sediment layer lead to the release of Hg species into the water column. Eutrophication and/or restricted vertical mixing lead to reducing conditions and intensify MeHg formation in the sediment with periodic release to the water column. Oxygenation of an anoxic water body can lead to the appearance of Hg species in the water column and uptake by organisms, whereby Hg may enter into the food web. The comparison of studied scenarios shows that a well-oxygenated eutrophic system favors the conditions for Hg species bioaccumulation with a potential adverse effect on the ecosystem. The research is relevant to the UN Minimata convention, EU policies on water, environmental quality standards and Mercury in particular.
Frontiers Media S.A.
2018
American Geophysical Union (AGU)
2018
Simulating CH4 and CO2 over South and East Asia using the zoomed chemistry transport model LMDz-INCA
The increasing availability of atmospheric measurements of greenhouse gases (GHGs) from surface stations can improve the retrieval of their fluxes at higher spatial and temporal resolutions by inversions, provided that transport models are able to properly represent the variability of concentrations observed at different stations. South and East Asia (SEA; the study area in this paper including the regions of South Asia and East Asia) is a region with large and very uncertain emissions of carbon dioxide (CO2) and methane (CH4), the most potent anthropogenic GHGs. Monitoring networks have expanded greatly during the past decade in this region, which should contribute to reducing uncertainties in estimates of regional GHG budgets. In this study, we simulate concentrations of CH4 and CO2 using zoomed versions (abbreviated as "ZAs") of the global chemistry transport model LMDz-INCA, which have fine horizontal resolutions of ∼ 0.66° in longitude and ∼ 0.51° in latitude over SEA and coarser resolutions elsewhere. The concentrations of CH4 and CO2 simulated from ZAs are compared to those from the same model but with standard model grids of 2.50° in longitude and 1.27° in latitude (abbreviated as "STs"), both prescribed with the same natural and anthropogenic fluxes. Model performance is evaluated for each model version at multi-annual, seasonal, synoptic and diurnal scales, against a unique observation dataset including 39 global and regional stations over SEA and around the world. Results show that ZAs improve the overall representation of CH4 annual gradients between stations in SEA, with reduction of RMSE by 16–20% compared to STs. The model improvement mainly results from reduction in representation error at finer horizontal resolutions and thus better characterization of the CH4 concentration gradients related to scattered distributed emission sources. However, the performance of ZAs at a specific station as compared to STs is more sensitive to errors in meteorological forcings and surface fluxes, especially when short-term variabilities or stations close to source regions are examined. This highlights the importance of accurate a priori CH4 surface fluxes in high-resolution transport modeling and inverse studies, particularly regarding locations and magnitudes of emission hotspots. Model performance for CO2 suggests that the CO2 surface fluxes have not been prescribed with sufficient accuracy and resolution, especially the spatiotemporally varying carbon exchange between land surface and atmosphere. In addition, the representation of the CH4 and CO2 short-term variabilities is also limited by model's ability to simulate boundary layer mixing and mesoscale transport in complex terrains, emphasizing the need to improve sub-grid physical parameterizations in addition to refinement of model resolutions.
2018
While feathers have been successfully validated for monitoring of internal concentrations of heavy metals and legacy persistent organic pollutants (POPs), less is known about their suitability for monitoring ofemerging con- taminants (ECs). Our study presents a broad investigation ofboth legacy POPs and ECs in non-destructivematri- ces from a bird of prey. Plasma and feathers were sampled in 2015 and 2016 from 70 whitetailed eagle (Haliaeetus albicilla) nestlings from two archipelagos in Norway. Preen oil was also sampled in 2016. Samples were analysed for POPs (polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) and organochlorinated pesticides (OCPs)) and ECs (per- and polyfluoroalkyl substances (PFASs), dechlorane plus (DPs), phosphate and novel brominated flame retardants (PFRs and NBFRs)). A total of nine PCBs, three OCPs, one PBDE and one PFAS were detected in over 50% of the plasma and feather samples within each sampling year and location. Significant and positive correlationswere found between plasma, feathers and preen oil concentrations of legacy POPs and confirm the findings ofprevious research on the usefulness of these matrices for non-destructive mon- itoring. In contrast, the suitability of feathers for ECs seems to be limited. Detection frequencies (DF) of PFASs were higher in plasma (mean DF: 78%) than in feathers (mean DF: 38%). Only perfluoroundecanoic acid could be quantified in over 50% ofboth plasma and feather samples, yet their correlation was poor and not significant. The detection frequencies of PFRs, NBFRs and DPs were very low in plasma (mean DF: 1–13%), compared to feathers (meanDF: 10–57%). Thismay suggest external atmospheric deposition, rapid internal biotransformation or excretion of these compounds. Accordingly, we suggest prioritising plasma for PFASs analyses, while the sources of PFRs, NBFRs and DPs in feathers and plasma need further investigation.
Elsevier
2018
A portion of Colombia’s water resources is located on the Pacific coast within the territory of the Community Council of Alto and Medio Dagua (CC-AMDA). Though a harmonious balance between the communities’ subsistent activities and nature was maintained for centuries, the appearance of modern modes of resource extraction has negatively affected the environment, especially the water resources. The Driver-Pressure-State- Impact-Response (DPSIR) framework was used to analyze water quality problems within this community council. The DPSIR analysis revealed that agriculture, mining, logging and infrastructure development constitute important sectoral drivers with some contribution from tourism and fisheries. Pressures included inputs of organic matter, sediment, nutrients and chemical contaminants to the Dagua river, and to the Bay of Buenaventura. These produced corresponding State changes in the water bodies. Impacts on human welfare were poor public health, reduced food and water security, economic loss and some displacement. Societal Responses included public protests and campaigns, legal actions and policy changes for improved governance. As a future policy option, the formation of community-based water resources management is recommended. Though DPSIR was able to link cause-effect relations, further empirical research on these water bodies is necessary to fill in existing gaps in the data set, particularly for public health threatening contaminants.
Taylor & Francis
2018