The Differentiation of Point Symbols using Selected Visual Variables in the Mobile Augmented Reality System

On the basis of initial studies devoted to a better understanding of how the public user (a pedestrian in the city) perceives cartographic symbols in the mobile augmented reality system, we present an attempt to determine the threshold values of differentiation for three visual variables. The variables of size, transparency, and focus were implemented into image point symbols representing five types of objects. The set of symbols was designed in accordance with the rules of cartographic design taking into consideration an analysis of 19 professional tourist works. The symbols were presented on the screen of a mobile device in a system imitating the augmented reality system against four different backgrounds: white, a wall, and two typical urban landscapes. The results of an internet survey conducted using a tablet at four locations in Poznan (Poland) allowed us to determine the following: threshold differentiation values for the analysed variables, indication of the dependence on the type of background displayed on the mobile device in augmented reality, and the advantage of using a combination of visual variables.     

Mercury mobility and bioavailability in soil from contaminated area

The mobility and bioavailability of mercury in the soil from the area near a plant using elemental mercury for manufacturing thermometers, areometers, glass energy switches and other articles made of technical glass has been evaluated. Mercury has been determined by sequential extraction method and with additional thermo desorption stage to determine elemental mercury. The procedure of sequential extraction involves five subsequent stages performed with the solutions of chloroform, deionized water, 0.5 M HCl, 0.2 M NaOH and aqua regia. The mean concentration of total mercury in soil was 147 ± 107 μg g⁻¹ dry mass (range 62–393), and the fractionation revealed that mercury was mainly bound to sulfides 56 ± 8% (range 45–66), one of the most biounavailable and immobile species of mercury in the environment. The fractions that brought lower contribution to the total mercury content were semi-mobile humic matter 22 ± 9% (range 11–34) and elemental mercury 17 ± 5% (range 8–23). The contributions brought by the highly mobile and toxic organomercury compounds were still lower 2.3 ± 2.7% (range 0.01–6.5). The lowest contributions brought the acid-soluble mercury 1.5 ± 1.3% (range 0.1–3.5) and water-soluble mercury 1.0 ± 0.3% (range 0.6–1.7). The surface layer of soil (0–20 cm) was characterized by higher mercury concentrations than that of the subsurface soil (60–80 cm), but the fractional contributions were comparable. The comparison of mercury fractionation results obtained in this study for highly polluted soils with results of fractionation of uncontaminated or moderately contaminated samples of soil and sediments had not shown significant statistical differences; however, in the last samples elemental mercury is usually present at very low concentrations. On the basis of obtained correlation coefficients it seems that elemental mercury soils from “Areometer” plant are contaminated; the main transformation is its vaporization to atmosphere and oxidation to divalent mercury, probably mainly mediated by organic matter, and next bound to humic matter and sulfides.     

Geochemical features of re-deposited organic matter occurring in fluvioglacial sediments in the Racibórz region (Poland): A case study

The erosion of rocks rich in organic matter typically leads to the complete mineralization of the organic material. However, in some cases, it is re-deposited to become a part of sediments once more. This process should be considered to be a part of global carbon cycle, possibly much more significant than assumed to-date. The research presented here aims to characterize re-worked organic matter occurring in post-glacial sediments of southern part of Poland, in the Oder river valley (the Racibórz town region, Miocene, Pleistocene and Holocene age). Organic substances extracted from the sediments originated from organic matter that had resided in rocks eroded by glaciers. Sediments were sampled in two boreholes which sediments were correlated. Sediments were extracted and extracts analyzed with gas chromatography-mass spectrometry (GC-MS) to assess distributions of biomarker groups. Organic matter of selected samples was pre-concentrated and analyzed with Py/GC-MS. In the extracts several biomarker parameters of source/environment and thermal maturity were calculated. Organic substances in the investigated sediments come from variable re-deposited organic matter occurring in rocks eroded by glaciers. Three main parent types of re-deposited organic material are identified showing variable geochemical features: 1) organic matter of recent or almost recent age being the source of polar labile compounds; probably formed in situ, 2) re-deposited organic matter of the middle diagenesis showing features similar to lignites (huminite reflectance Rf ~ 0.25–0.35%) deriving from angiosperm remains, mainly monocotyledons and to the lower extend also deciduous trees, 3) re-deposited organic matter at the middle catagenesis (Rf ~ 0.65–0.75%) being the source of most of aromatic hydrocarbons and biomarkers such as steranes, hopanes of the more thermally advanced distribution type. Its geochemical properties and assumed directions of sediment transport indicate bituminous coals of Upper Silesian Coal Basin together with coaly shales as a possible source of this organic matter. Such mixed origin of organic matter caused large discrepancies in values of thermal maturity parameters depending on input from the particular sources and occurrence both geochemical biomarkers and their biochemical precursors in the same samples.     

Geochemical characteristics of the macromolecular part of crude and biodesulphurised flame coal density fractions

Flame coal (Janina Mine, Poland) was an object of geochemical analyses for changes caused by the process of microbial desulphurisation. Ash content, beryllium, chromium, zinc, cobalt, lithium, manganese, copper, molybdenum, nickel, lead and vanadium concentrations were investigated in coal extracts, its macromolecular part, semi-coke and polar compound fractions of extracts and pyrolysates of crude and biodesulphurised coal density fractions. The macromolecular part of extracted density fractions was pyrolysed giving semi-coke and pyrolysate. These were separated into aliphatic hydrocarbons, aromatic and polar compounds by thin layer chromatography (TLC). Distributions of aliphatic and aromatic hydrocarbons in pyrolysates of the crude and desulphurised coal density fractions were compared by gas chromatography-mass spectrometry (GC-MS). Extracts, extracted density fractions, semi-coke and polar compound fractions were analysed for concentrations of trace elements. In the crude coal their concentrations in the macromolecular part are related only to coke. However, in the desulphurised coal the participation of the particular trace element increases in pyrolysate polar compound fractions. Its values are in the range from 1% (Mn) to 100% (Cr and Mo). These changes are the best seen in the 1.80-2.30×10³ kg/m³ density fraction. Very high concentrations of trace elements were found in pyrolysate of desulphurised coal density fraction. This can be explained by the partial decomposition of coal macromolecule resulting from desulphurisation. Significant side-cleavage of peripheral groups and lighter aromatic hydrocarbons is possible. The effects of bacterial influence were manifested by the increase of polar compounds contents both in pyrolysates and extracts of the desulphurised coal and changes in distribution of aliphatic and aromatic hydrocarbon as pyrolytical products. These effects increase with mineral substance contents. Moreover, the increase of trace element concentration in coal organic matter occurs. It is reflected by the increase of participation of coal pyrolysate polar fraction in the total concentration of analysed elements in the macromolecular part of a given density fraction. The presented results are a part of the larger research aimed to find an influence of desulphurisation on chemical and technological properties of coal.     

Effects of long term nutrient and climate variability on subfossil Cladocera in a deep,subalpine lake (Lake Garda,northern Italy)

Albeit subfossil Cladocera remains are considered as a reliable proxy for tracking historical lake development, they have been scarcely studied in large subalpine lakes south of the Alps. In this study, subfossil Cladocera remains from Lake Garda in northern Italy were analyzed to track the lake’s environmental changes since the Middle Ages. One core was retrieved from the largest sub-basin of Lake Garda (Brenzone, 350 m deep) and two cores were retrieved from the profundal and littoral zone of the smaller lake sub-basin (Bardolino, 80 and 40 m deep, respectively). The species distribution of Cladocera remains in recent sediment layers was similar to that observed in contemporary water samples. The deepest sections of the three cores were characterized by species sensitive to water temperature, which suggest a key role of major climatic events in driving the lake response during the late Holocene. The most evident change in Cladocera assemblages in the studied cores was observed during the 1960s, when planktonic taxa such as Daphnia spp. and Bosmina spp. became dominant at the expense of littoral taxa. Despite the highly coherent general pattern of subfossil Cladocera, the cores showed a set of minor differences, which were attributed to different morphological and hydrological features of the two basins forming Lake Garda. Multivariate analysis revealed a clear relation of Cladocera to climate variability during periods of low lake nutrient levels (i.e. before the 1960s). This provides additional information on past ecological responses of Lake Garda, as contrast previous data from subfossil diatom and pigment analyses did not fully capture effects of climate change during the same period. Since the 1960s shifts in assemblage composition of Cladocera and diatoms were highly coherent, in response to nutrient increase and the following, less pronounced, decrease in nutrient concentrations. During the last five decades, the response of the Cladocera to climate variability appeared to be masked by nutrient change. This work points up the potential of the multi-proxy approach for disentangling the multifaceted biological responses to multiple environmental stressors in large and deep lakes.     

Water level changes in Polish lakes during 1976–2010

The paper presents the analysis of tendencies in water level changes in 32 lakes in Poland during 1976–2010. Series of monthly, seasonal, and annual precipitation and air temperature for 9 meteorological stations were also studied. The trend analysis for all of the studied series of water levels in lakes showed high spatial and temporal variability. Series of annual water levels in the case of 6 lakes showed statistically significant increasing tendencies, and in 7 lakes, significant decreasing trends. Series of annual amplitudes in the majority of lakes (22) showed a decreasing trend, but they were statistically significant only in three cases. The tendencies for air temperature fluctuations are more statistically significant than precipitation. The key role in determining water level changes is played by local factors, particularly including human economic activity, obscuring the effect of natural factors on water level changes. The paper describes cases of changes in water levels in lakes under anthropopressure related to among others: agricultural irrigations, hydropower infrastructure, water transfers, navigation, or mining.     

Evaluation of Trends and Changes in the Gulf of Gdańsk Ecosystem—an Integrated Approach

An integrated trend assessment was conducted for the Gulf of Gdańsk (GoG), Baltic Sea for the period 1994–2010 to describe changes and potentially important drivers of the ecosystem. We found changes in the biota, including an increase in open sea taxa (flatfish, sprat and cod), a decrease in typical coastal species such as eelpout and lumpfish and an increase in primary production. The analyses further suggest that changes in the food web were driven by a combination of anthropogenic pressures (e.g., nutrient loadings and fisheries) and possible interactions with climatic disturbance. Our analyses show that significant changes occurred in the GoG ecosystem between 1994 and 2010. The primary drivers and mechanisms of these changes are discussed. We describe this alteration of the GoG within the context of similar temporal patterns identified in adjacent areas.     

Physical and chemical characteristics of after-reclamation dust from used sand moulds

The paper presents the results of investigations of physical and chemical properties of after reclamation dust that is generated in the foundry industry. Universally applied mechanical reclamation processes of spent moulding sands generate large amounts of after-reclamation dusts containing mainly rubbed spent binding agents and quartz dusts. An amount of after-reclamation dusts—in dependence of the reclamation system efficiency and the reclaim dedusting system—can reach 5–10 % in relation to the total reclaimed spent moulding sand. After-reclamation dusts originated from spent moulding sands with different kinds of resins mostly belong to dangerous wastes, since they contain chemo-setting binders with dangerous substances removed in the reclamation process. None of the companies producing mechanical reclamation systems offers presently the complex technology and equipment for utilisation of after reclamation dusts, which would meet technical and economic expectations of foundry plants. The paper presents the results of research carried out at the Faculty of Foundry Engineering AGH UST in Cracow which aims on the determination of possibilities of using the post-reclamation dust generated during mechanical reclamation of used moulding sands with organic resins as a source of energy. Different dusts generated in the mechanical reclamation process of used organic sands, delivered from foundries, were tested to determine their chemical composition, granular characterisation and physicochemical properties. As a result of the investigations, possible ways to utilise the dusts are presented.