Fant 2627 publikasjoner. Viser side 81 av 263:
A combination of local (i.e. firefighting training facilities) and remote sources (i.e., long-range transport) are assumed to be responsible for the occurrence of per- and polyfluoroalkyl substances (PFASs) in Svalbard (Norwegian Arctic). However, no systematic elucidation of local PFASs sources have been conducted yet. Therefore, a survey was performed aiming at identifying local PFASs pollution sources on the island of Spitsbergen (Svalbard, Norway). Soil, fresh water (lake, draining rivers), sea water, melt-water run-off, surface snow and coastal sediment samples were collected from Longyearbyen (Norwegian mining town), Ny-Ålesund (research facility) and the Lake Linnévatnet area (background site) during several campaigns (2014-2016) and analysed for 14 individual target PFASs. For background site (Linnévatnet area, sampling during April to June 2015), ∑PFAS levels ranged from 0.4 – 4 ng/L in surface lake water (n = 20). PFAS in melt water from the contributing glaciers showed similar concentrations (~4 ng/L, n = 2). The short chain perfluorobutanoate (PFBA) was predominant in lake water (60-80% of the ∑PFASs), meltwater (20-30 %) and run-off water (40 %). Long range transport is assumed to be the major PFAS source. In Longyearbyen, 5 water samples (i.e. 2 seawater, 3 run-off) were collected near the local firefighting training site (FFTS) in November 2014 and June 2015, respectively. The highest PFAS levels were found in FFTS melt water run-off (118 ng/L). PFOS was the most abundant compound in the FFTS meltwater run-off (53 – 58 % PFASs). At the research station Ny-Ålesund, sea water (n = 6), soil (n = 9) and fresh water (n = 10) were collected in June 2016. Low ∑PFAS concentrations were determined for sea water (5 - 6 ng/L), whereas high ∑PFAS concentrations were found in run-off water (113 – 119 ng/L) and soil (211 – 800 ng/g dry weight (dw)) collected close to the local FFTS. In addition, high ∑PFAS levels (127 ng/L) were also found in fresh water from lake Solvatnet close to former sewage treatment facility. Overall, at both FFTS affected sites (soil, water), PFOS was the most abundant compound (60 – 69% of ∑PFASs). FFTS and landfill locations were identified as major PFASs sources for Svalbard settlements.
2018
Mineral Dust Instantaneous Radiative Forcing in the Arctic
American Geophysical Union (AGU)
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
Exposure to airborne fine particulate matter (PM2.5) carries substantial health risks, particularly for younger children (0–10 years). Epidemiological evidence indicates that children are more susceptible to PM health effects than adults. We conducted a literature review to obtain an overview of existing knowledge regarding the correlation of exposure to short- and long-term PM concentrations with respiratory symptoms and disease in children. A collection of scientific papers and topical reviews were selected in cooperation with two experienced paediatricians. The literature review was performed using the keywords “air pollution”, “particulate matter”, “children’s health” and “respiratory” from 1950 to 2016, searching the databases of Scopus, Google Scholar, Web of Science, and PubMed. The search provided 45,191 studies for consideration. Following the application of eligibility criteria and experts’ best judgment to titles and abstracts, 28 independent studies were deemed relevant for further detailed review and knowledge extraction. The results showed that most studies focused mainly on the effect of short-term exposure in children, and the reported associations were relatively homogeneous amongst the studies. Most of the respiratory diseases observed in outdoor studies were related to changes in lung function and exacerbation of asthma symptoms. Allergic reactions were frequently reported in indoor studies. Asthma exacerbation, severe respiratory symptoms and moderate airway obstruction on spirometry were also observed in children due to various sources of indoor pollution in households and schools. Mixed indoor and outdoor studies indicate frequent occurrence of wheezing and deterioration of lung function. There is good evidence of the adverse effect of short-term exposure to PM on children’s respiratory health. In terms of long-term exposure, fine particles (PM0.1–PM2.5) represent a higher risk factor than coarse particles (PM2.5–PM10). Additional research is required to better understand the heterogeneous sources and the association of PM and adverse children’s health outcomes. We recommend long-term cooperation between air quality specialists, paediatricians, epidemiologists, and parents in order to improve the knowledge of PM effects on young children’s respiratory health.
MDPI
2018
Assessment of spatial and temporal variation in the impacts of ozone on human health, vegetation, and climate requires appropriate metrics. A key component of the Tropospheric Ozone Assessment Report (TOAR) is the consistent calculation of these metrics at thousands of monitoring sites globally. Investigating temporal trends in these metrics required that the same statistical methods be applied across these ozone monitoring sites. The nonparametric Mann-Kendall test (for significant trends) and the Theil-Sen estimator (for estimating the magnitude of trend) were selected to provide robust methods across all sites. This paper provides the scientific underpinnings necessary to better understand the implications of and rationale for selecting a specific TOAR metric for assessing spatial and temporal variation in ozone for a particular impact. The rationale and underlying research evidence that influence the derivation of specific metrics are given. The form of 25 metrics (4 for model-measurement comparison, 5 for characterization of ozone in the free troposphere, 11 for human health impacts, and 5 for vegetation impacts) are described. Finally, this study categorizes health and vegetation exposure metrics based on the extent to which they are determined only by the highest hourly ozone levels, or by a wider range of values. The magnitude of the metrics is influenced by both the distribution of hourly average ozone concentrations at a site location, and the extent to which a particular metric is determined by relatively low, moderate, and high hourly ozone levels. Hence, for the same ozone time series, changes in the distribution of ozone concentrations can result in different changes in the magnitude and direction of trends for different metrics. Thus, dissimilar conclusions about the effect of changes in the drivers of ozone variability (e.g., precursor emissions) on health and vegetation exposure can result from the selection of different metrics.
2018
2018
The safety of high quality drinking water supply relies on the quantities to be delivered, on the complexity of the water supply systems, and on the widespread phenomena of the contamination of water bodies. These parameters indicate the need for the development of an application that will allow the quick acquisition of data on strategic management. This is requires both the analysis of factors related to the hydraulic operation of the plants and the characteristics of water quality. The present paper aims to evaluate the use of models that predict data for water quality in a distribution system. The assessment is made in order to consider the use of the model as a support tool for the management system of a supply network and to optimize the quality of the provided service. The improvement of the control system related to the operations of disinfection, in particular, in the case of long pipelines, is absolutely mandatory in order to ensure the safety of public health and respect for the environment at high levels.
MDPI
2018
Signals from the south; humpback whales carry messages of Antarctic sea‐ice ecosystem variability
John Wiley & Sons
2018