scholarly journals Měkkýši hradů Sion a Vízmburk – sukcese na znovuobjevených zříceninách [Molluscs of Sion and Vízmburk castles – succession on the reappearance ruins of castles]

2003 ◽  
Vol 2 ◽  
pp. 55-57 ◽  
Author(s):  
Lucie Juřičková
Keyword(s):  
Long Range ◽  
Indirect Evidence ◽  
Long Range Transport ◽  
Range Transport

Castles Sion near Kutná Hora and Vízmburk near Trutnov were completely excavated 40 and 30 years ago. We can therefore monitor the succession in these localities. In the castle Sion there now live 32 species (with species isolated in this locality Helicodonta obvoluta and Causa holosericea). 12 species living in Vízmburk is also a relatively high number in view of the fact that this castle is completely isolated in spruce monoculture. These castles are indirect evidence of long-range transport of snails by birds and other animals. Both localities represent the long-term ecologic experiment.

scholarly journals Měkkýši hradů Sion a Vízmburk – sukcese na znovuobjevených zříceninách [Molluscs of Sion and Vízmburk castles – succession on the reappearance ruins of castles]

2003 ◽  
Vol 2 ◽  
pp. 55-57
Author(s):  
Lucie Juřičková
Keyword(s):  
Long Range ◽  
Indirect Evidence ◽  
Long Range Transport ◽  
Range Transport

Castles Sion near Kutná Hora and Vízmburk near Trutnov were completely excavated 40 and 30 years ago. We can therefore monitor the succession in these localities. In the castle Sion there now live 32 species (with species isolated in this locality Helicodonta obvoluta and Causa holosericea). 12 species living in Vízmburk is also a relatively high number in view of the fact that this castle is completely isolated in spruce monoculture. These castles are indirect evidence of long-range transport of snails by birds and other animals. Both localities represent the long-term ecologic experiment.

scholarly journals Parametrisation of the orographic enhancement of precipitation and deposition in a long-term, long-range transport model

2000 ◽  
Vol 18 (11) ◽  
pp. 1447-1466 ◽  
Author(s):  
D. S. Lee ◽  
R. D. Kingdon ◽  
J. A. Garland ◽  
B. M. R. Jones
Keyword(s):  
Sulfur Dioxide ◽  
Long Range ◽  
Wet Deposition ◽  
Enhancement Factor ◽  
Long Range Transport ◽  
Orographic Precipitation ◽  
Range Transport ◽  
Orographic Enhancement ◽  
The Uk

Abstract. Orographic enhancement of wet deposition arising from the 'seeder-feeder' effect is, by necessity, highly parametrised in long-range transport models of acid deposition that are long-term (i.e. annual average) and spatially resolved at tens of kilometres. Here, we describe a mechanistic approach to the incorporation of these mechanisms into such a model. The model formulation required the following: precipitation rate by direction and quantification of the fractions that are orographic and non-orographic; treatment of the fast oxidation of sulfur dioxide in clouds; the directionality of the seeder-feeder process; and a quantitative basis for increasing wet deposition factors to account for the seeder-feeder process. The directionality of non-orographic precipitation was determined from meteorological data at 47 sites across the UK. Orographic precipitation varies on a much finer scale than can be interpolated from measurements, and thus a modelling approach was adopted. The directionality of the seeder-feeder effect was taken from measurements. The enhancement factor of the orographic component of precipitation, assumed to represent feeder-rain, was determined from a review of measurements. Fast oxidation of sulfur dioxide is an observed phenomenon in cap-cloud, but limited in duration. An adjustment was made to the sulfur dioxide oxidation rate in the model in locations where cap-cloud was assumed to be present. The results from the model were compared with UK deposition budgets and enhanced wet deposition maps. The revised parametrisation underestimated the UK wet deposition budgets of oxidised N and S, but spatial patterns of deposition were improved for much of the UK. It was concluded that this was a satisfactory outcome given the constraints of the statistical approach of weighting of deposition at receptors utilising straight line trajectories. The sensitivity of the model to directional constraints of seeder-feeder enhancement was tested and it was concluded that a fairly narrow constraint resulted in similar estimations to a broader one, and the broader constraint was thus adopted as frontal conditions which result in the process arrive from a fairly broad band of directions. When enhancement was allowed to occur from all directions, UK wet deposition of oxidised N and S was increased by 10%. The sensitivity to the enhancement factor on wet deposition was tested and found to be relatively robust. An increase in the enhancement factor from 2 to 6 resulted in increases in UK wet deposition of oxidised N and S of 9 and 6%, respectively.Key words: Atmospheric composition and structure (pollution – urban and regional) – Meteorology and atmospheric dynamics (precipitation)

scholarly journals Long-term measurements of carbonaceous aerosols in the Eastern Mediterranean: evidence of long-range transport of biomass burning

2008 ◽  
Vol 8 (18) ◽  
pp. 5551-5563 ◽  
Author(s):  
J. Sciare ◽  
K. Oikonomou ◽  
O. Favez ◽  
E. Liakakou ◽  
Z. Markaki ◽  
...  
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Long Range ◽  
Biomass Burning ◽  
Water Soluble ◽  
Long Range Transport ◽  
Crete Island ◽  
Yearly Average ◽  
Range Transport

Abstract. Long-term (5-year) measurements of Elemental Carbon (EC) and Organic Carbon (OC) in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island). A multi-analytical approach (including thermal, optical, and thermo-optical techniques) was applied for these EC and OC measurements. Light absorbing dust aerosols were shown to poorly contribute (+12% on a yearly average) to light absorption coefficient (babs) measurements performed by an optical method (aethalometer). Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September). The contribution of biomass burning to the concentrations of EC and OC was shown to be rather small (20 and 14%, respectively, on a yearly basis), although this contribution could be much higher on a monthly basis and showed important seasonal and interannual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC) have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12), suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA) formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5μm) showed that the mass contribution of organic matter (POM) was found to be essentially invariable during the year (monthly average of 26±5%).

scholarly journals Long-term measurements of carbonaceous aerosols in the eastern Mediterranean: evidence of long-range transport of biomass burning

2008 ◽  
Vol 8 (2) ◽  
pp. 6949-6982 ◽  
Author(s):  
J. Sciare ◽  
K. Oikonomou ◽  
O. Favez ◽  
Z. Markaki ◽  
E. Liakakou ◽  
...  
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Long Range ◽  
Biomass Burning ◽  
Water Soluble ◽  
Long Range Transport ◽  
Crete Island ◽  
Yearly Average ◽  
Range Transport

Abstract. Long-term (5-yr) measurements of Black Carbon (BC) and Organic Carbon (OC) in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island). A multi-analytical approach (including thermal, optical, and thermo-optical techniques) was applied for these BC and OC measurements. Light absorbing dust aerosols have shown to poorly contribute (+17% on a yearly average) to light absorption coefficient (babs) measurements performed by an optical method (aethalometer). Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September). The contribution of biomass burning to the concentrations of BC and OC has shown to be rather small (20 and 14%, respectively, on a yearly basis), although this contribution could be much higher on a monthly basis and is expected a high intra and inter annual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the Spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC) have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12), suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA) formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5 μm) showed that the mass contribution of organic matter (POM) was found to be essentially invariable during the year (monthly average of 26±5%).

scholarly journals Long-term monitoring of persistent organic pollutants (POPs) at the Norwegian Troll station in Dronning Maud Land, Antarctica

2013 ◽  
Vol 13 (14) ◽  
pp. 6983-6992 ◽  
Author(s):  
R. Kallenborn ◽  
K. Breivik ◽  
S. Eckhardt ◽  
C. R. Lunder ◽  
S. Manø ◽  
...  
Keyword(s):  
Long Range ◽  
Organic Pollutants ◽  
Persistent Organic Pollutants ◽  
Long Range Transport ◽  
Research Station ◽  
Range Transport ◽  
Dronning Maud Land ◽  
Long Term Monitoring ◽  
Term Monitoring

Abstract. A first long-term monitoring of selected persistent organic pollutants (POPs) in Antarctic air has been conducted at the Norwegian research station Troll (Dronning Maud Land). As target contaminants 32 PCB congeners, α- and γ-hexachlorocyclohexane (HCH), trans- and cis-chlordane, trans- and cis-nonachlor, p,p'- and o,p-DDT, DDD, DDE as well as hexachlorobenzene (HCB) were selected. The monitoring program with weekly samples taken during the period 2007–2010 was coordinated with the parallel program at the Norwegian Arctic monitoring site (Zeppelin mountain, Ny-Ålesund, Svalbard) in terms of priority compounds, sampling schedule as well as analytical methods. The POP concentration levels found in Antarctica were considerably lower than Arctic atmospheric background concentrations. Similar to observations for Arctic samples, HCB is the predominant POP compound, with levels of around 22 pg m−3 throughout the entire monitoring period. In general, the following concentration distribution was found for the Troll samples analyzed: HCB > Sum HCH > Sum PCB > Sum DDT > Sum chlordanes. Atmospheric long-range transport was identified as a major contamination source for POPs in Antarctic environments. Several long-range transport events with elevated levels of pesticides and/or compounds with industrial sources were identified based on retroplume calculations with a Lagrangian particle dispersion model (FLEXPART).

Long-range transport and regional sources of PM2.5 in Beijing based on long-term observations from 2005 to 2010

2015 ◽  
Vol 157 ◽  
pp. 37-48 ◽  
Author(s):  
Lili Wang ◽  
Zirui Liu ◽  
Yang Sun ◽  
Dongsheng Ji ◽  
Yuesi Wang
Keyword(s):  
Long Range ◽  
Long Range Transport ◽  
Regional Sources ◽  
Range Transport

scholarly journals Long-term chemical characterization of tropical and marine aerosols at the Cape Verde Atmospheric Observatory (CVAO) from 2007 to 2011

2014 ◽  
Vol 14 (17) ◽  
pp. 8883-8904 ◽  
Author(s):  
K. W. Fomba ◽  
K. Müller ◽  
D. van Pinxteren ◽  
L. Poulain ◽  
M. van Pinxteren ◽  
...  
Keyword(s):  
Long Range ◽  
Mineral Dust ◽  
Chemical Characterization ◽  
Sea Salt ◽  
Saharan Dust ◽  
Long Range Transport ◽  
Air Mass ◽  
Aerosol Mass ◽  
Range Transport

Abstract. The first long-term aerosol sampling and chemical characterization results from measurements at the Cape Verde Atmospheric Observatory (CVAO) on the island of São Vicente are presented and are discussed with respect to air mass origin and seasonal trends. In total 671 samples were collected using a high-volume PM10 sampler on quartz fiber filters from January 2007 to December 2011. The samples were analyzed for their aerosol chemical composition, including their ionic and organic constituents. Back trajectory analyses showed that the aerosol at CVAO was strongly influenced by emissions from Europe and Africa, with the latter often responsible for high mineral dust loading. Sea salt and mineral dust dominated the aerosol mass and made up in total about 80% of the aerosol mass. The 5-year PM10 mean was 47.1 &amp;pm; 55.5 μg m−2, while the mineral dust and sea salt means were 27.9 &amp;pm; 48.7 and 11.1 &amp;pm; 5.5 μg m−2, respectively. Non-sea-salt (nss) sulfate made up 62% of the total sulfate and originated from both long-range transport from Africa or Europe and marine sources. Strong seasonal variation was observed for the aerosol components. While nitrate showed no clear seasonal variation with an annual mean of 1.1 &amp;pm; 0.6 μg m−3, the aerosol mass, OC (organic carbon) and EC (elemental carbon), showed strong winter maxima due to strong influence of African air mass inflow. Additionally during summer, elevated concentrations of OM were observed originating from marine emissions. A summer maximum was observed for non-sea-salt sulfate and was connected to periods when air mass inflow was predominantly of marine origin, indicating that marine biogenic emissions were a significant source. Ammonium showed a distinct maximum in spring and coincided with ocean surface water chlorophyll a concentrations. Good correlations were also observed between nss-sulfate and oxalate during the summer and winter seasons, indicating a likely photochemical in-cloud processing of the marine and anthropogenic precursors of these species. High temporal variability was observed in both chloride and bromide depletion, differing significantly within the seasons, air mass history and Saharan dust concentration. Chloride (bromide) depletion varied from 8.8 &amp;pm; 8.5% (62 &amp;pm; 42%) in Saharan-dust-dominated air mass to 30 \\textpm 12% (87 &amp;pm; 11%) in polluted Europe air masses. During summer, bromide depletion often reached 100% in marine as well as in polluted continental samples. In addition to the influence of the aerosol acidic components, photochemistry was one of the main drivers of halogenide depletion during the summer; while during dust events, displacement reaction with nitric acid was found to be the dominant mechanism. Positive matrix factorization (PMF) analysis identified three major aerosol sources: sea salt, aged sea salt and long-range transport. The ionic budget was dominated by the first two of these factors, while the long-range transport factor could only account for about 14% of the total observed ionic mass.

scholarly journals The role of long-range transport and domestic emissions in determining atmospheric secondary inorganic particle concentrations across the UK

2013 ◽  
Vol 13 (12) ◽  
pp. 33433-33462
Author(s):  
M. Vieno ◽  
M. R. Heal ◽  
S. Hallsworth ◽  
D. Famulari ◽  
R. M. Doherty ◽  
...  
Keyword(s):  
Long Range ◽  
Regional Scale ◽  
Long Range Transport ◽  
Substantial Part ◽  
Limit Values ◽  
Substantial Impact ◽  
Inorganic Particle ◽  
Range Transport ◽  
The Uk

Abstract. Surface concentrations of secondary inorganic particle components over the UK have been analysed for 2001–2010 using the EMEP4UK regional atmospheric chemistry transport model. In early 2003 an episode of substantially elevated surface concentrations of ammonium nitrate was measured across the UK by the AGANET network. The EMEP4UK model was able accurately to represent both the long-term decadal surface concentrations and the episode in 2003. The latter was identified as consisting of three separate episodes, each of less than 1 month duration, in February, March and April. The primary cause of the elevated nitrate levels across the UK was meteorological, a persistent high pressure system, but whose varying location impacted the relative importance of transboundary vs. domestic emissions. Whilst long-range transport dominated the elevated nitrate in February, in contrast it was domestic emissions that mainly contributed to the March episode, and for the April episode both domestic emissions and long-range transport contributed. A prolonged episode such as the one in early 2003 can have substantial impact on annual average concentrations. The episode led to annual concentration differences at the regional scale of similar magnitude to those driven by long-term changes in precursor emissions over the full decade investigated here. The results demonstrate that a substantial part of the UK, particularly the south and south-east, may be close to or actually exceeding annual mean limit values because of import of inorganic aerosol components from continental Europe under specific conditions. The results reinforce the importance of employing multiple year simulations in the assessment of emissions reduction scenarios on PM concentrations and the need for international agreements to address the transboundary component of air pollution.

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