International audience | This paper presents a new Remote Hyperspectral Imaging System (RHIS) embedded on an Unmanned Aquatic Drone (UAD) for plastic detection and identification in coastal and freshwater environments. This original system, namely the Remotely Operated Vehicle of the University of Littoral Côte d’Opale (ROV-ULCO), works in a near-field of view, where the distance between the hyperspectral camera and the water surface is about 45 cm. In this paper, the new ROV-ULCO system with all its components is firstly presented. Then, a hyperspectral image database of plastic litter acquired with this system is described. This database contains hyperspectral data cubes of different plastic types and polymers corresponding to the most-common plastic litter items found in aquatic environments. An in situ spectral analysis was conducted from this benchmark database to characterize the hyperspectral reflectance of these items in order to identify the absorption feature wavelengths for each type of plastic. Finally, the ability of our original system RHIS to automatically recognize different types of plastic litter was assessed by applying different supervised machine learning methods on a set of representative image patches of marine litter. The obtained results highlighted the plastic litter classification capability with an overall accuracy close to 90%. This paper showed that the newly presented RHIS coupled with the UAD is a promising approach to identify plastic waste in aquatic environments.

Hydrological, psamological and pluviographical measurements in experimental watershed area in the watershed of River Topciderska (Serbia, Yugoslavia) was analyzed. Interrelations between suspended sediment concentration in streams on the one hand and runoff, rainfall, rainfall intensity and index of previous rainfall on the other hand was came from this analyze. Effects of these parameters on suspended sediment concentration was considered for a single rainfall epizode, during the period of torrential waves and as annual value. Specific coefficients (coefficient of annual rainfall structure and coefficient of annual runoff structure) were used in this paper, with help of them effects of torrential waves and intensity rainfall on average annual suspended sediment concentration were considered.

Products of wet and dry deposition of aero-pollutants, reached by over-boundary or internal-boundary transport, are significant source of pollution, almost, whole territory of Serbia (Yugoslavia). Products of wet and dry deposition endangere surface storages in two ways: (1) directly, by deposition on surface storages; (2) indirectly, by deposition on surface of catchment areas, and further transporting through hydrographic system. In the period 1992-1996 investigations were carried out at some localities in Serbia (Yugoslavia). Their results show that recorded quantities significantly over pass MDK (maximal permitted quantity). Investigations included analysis of samples of precipitation (rain and snow), soil and sediment from hydrographic system.

The paper deals with the results of chemical analyses of the precipitation collected with the bulk method in and out of the pedunculate oak forest near Lipovljani in Croatia, for the period 1997-2001. A considerable higher total annual deposition of the majority of analysed determinants has been found in the forest. The results point to the importance and influence of the forest cover on the reception and distribution of dry and wet pollution in the forest ecosystem of pedunculate oak

This study incorporated stable isotope analyses with chemical analyses to determine the origin and migration of sulfur sources in East Asia, and these findings were compared with our decadal research from 2000 to 2001 and 2002 to 2003. The multiple sulfur isotope composition (32S, 33S and 34S) of the dissolved sulfate in precipitation was first measured from 2011 to 2013 in Seoul, South Korea. The δ34Snss values were −1.1‰ to 7.9‰ (avg. 3.6‰), strongly suggesting that sulfur derived from the combustion of Chinese coal is the predominant source of sulfate in the Seoul region. Low NO3/SO42− ratios in the precipitation samples indicated an insignificant effect of sulfur from vehicle exhaust. The seasonal variation of δ34Snss values appears to be caused by increasing biogenic sulfur activity during the spring and summer seasons. The some Δ33S values (0.13‰–0.16‰) measured in the three samples were sufficiently small; thus, whether these values can be attributed to mass-independent fractionation remains unclear. Measuring the Δ33S anomalies in dissolved sulfate provides valuable insights for identifying the sources of sulfur transferred from the stratosphere to the troposphere and upper troposphere.

In forest soils along vertical profiles located in different parts of the Alps, concentrations of persistent organic pollutants (POPs), namely organochlorine pesticides (OCPs) like dichlorodiphenyltrichloroethanes (DDTs), hexachlorobenzene (HCB), hexachlorocyclohexanes (HCH), heptachlor, aldrin, dieldrin and mirex, were measured. Though local characteristics of the sites are influenced by numerous factors like orographic and meteorological parameters, forest stand characteristics and humus parameters, we ascertained a marked vertical increase of concentrations of some organochlorine compounds in the soil. On the basis of climatological values of each site, we found that the contamination increase with altitude can be ascribed to a certain ‘cold condensation effect’. In addition, the perennial atmospheric deposition of POPs is controlled by precipitation. Other key parameters explaining the accumulation of POPs are the soil organic carbon stocks, the turnover times, the re-volatilisation and degradation processes, which vary with altitude. Caused by temperature-dependent processes regarding deposition, re-volatilization and decomposition of POPs, the concentration of organochlorine pesticides varies in the Alpine region with altitude.

Arsenic (As) pollution remains a major threat to the quality of global soils and drinking water. The health effects of As pollution are often severe and have been largely reported across Asia and South America. This study investigated the possibility of using unmodified biochar derived from rice husk (RB) and aspen wood (WB) at 400 °C and 700 °C to enhance the precipitation of calcium/arsenic compounds for the removal of As(III) from solution. The approach was based on utilizing calcium to precipitate arsenic in solution and adding unmodified biochar to enhance the process. Using this approach, As(III) concentration in aqueous solution decreased by 58.1% when biochar was added, compared to 25.4% in the absence of biochar. Varying the pH from acidic to alkaline enabled an investigation into the pH dependent dynamics of the approach. Results indicated that significant precipitation was only possible at near neutral pH (i.e. pH = 6.5) where calcium arsenites (i.e. Ca(AsO₂)₂, and CaAsO₂OH•½H₂O) and arsenates (i.e. Ca₅(AsO₄)₃OH) were precipitated and deposited as aggregates in the pores of biochars. Arsenite was only slightly precipitated under acidic conditions (pH = 4.5) while no arsenite was precipitated under alkaline conditions (pH = 9.5). Arsenite desorption from wood biochar was lowest at pH 6.5 indicating that wood biochar was able to retain a large quantity of the precipitates formed at pH 6.5 compared to pH 4.5 and pH 9.5. Given that the removal of As(III) from solution is often challenging and that biochar modification invites additional cost, the study demonstrated that low cost unmodified biochar can be effective in enhancing the removal of As(III) from the environment through Ca–As precipitation.

Phosphogypsum (PG) is disposed worldwide in large stacks usually placed in coastal zones, as in the case of Huelva (SW of Spain), where around 100 Mt of PG are stored on the salt marshes of the Tinto River estuary covering a surface of about 1000 ha. This management generates the weathering of PG, and due to its high acidity (pH ≈ 2) and pollutant load can provoke significant emissions into their surroundings. In this work were evaluated by laboratory experiments the effects of pH increase in the behaviour of heavy metals and natural radionuclides during the mixing of phosphogypsum leachates with seawater.The acidic phosphogypsum leachates showed concentrations of heavy metals from two to three orders of magnitude higher than natural continental waters, and natural radionuclides (U-isotopes and ²¹⁰Po) from four to five orders of magnitude higher than unperturbed aquatic systems. Major elements and some heavy metals as Mn, Ni, Cd, As, Sb and Co showed a conservative behaviour during the neutralisation of the leachates with seawater, remaining in the liquid phase, while other ones as Al, Fe, Cr, Zn, Cu, Pb precipitated and/or were adsorbed onto the solid phase. The U-isotopes and ²¹⁰Po showed a clear non-conservative behaviour probably due to coprecipitation/adsorption processes onto the formed precipitates, but while ²¹⁰Po reached a total removal at pH ≈ 7, U- isotopes after a total removal at pH ≈ 5 returned into the liquid phase due to redissolution/desorption processes at near neutral pH.The formed precipitates, mainly composed by iron phosphates particles, showed heavy metal and natural radionuclide concentrations from one to three orders of magnitude higher than unperturbed soils. All these facts demonstrate the serious environmental impact produced by the PG stacks into their surroundings and the urgency of effective restoration measures.