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.

Organic and mineral soil horizons from forests in 30 mountains across China were analysed for polychlorinated biphenyl (PCB). Soil total organic carbon (TOC) content was a key determinant of PCB distribution explaining over 90% of the differences between organic and mineral soils, and between 30% and 60% of the variance along altitudinal and regional transects. The residual variance (after normalization by TOC) was small. Tri- to tetra-CB levels were higher in the South in relation to high source density and precipitation. Heavier congeners were instead more abundant at mid/high-latitudes where the advection pattern was mainly from long range transport. This resulted in a latitudinal fractionation opposite to theoretical expectations. The study showed that exposure to sources with different characteristics, and possibly accumulation/degradation trends of different congeners in soils being out-of-phase at different latitudes, can lead to an unsteady large scale distribution scenario conflicting with the thermodynamic equilibrium perception.

Long-term substantial application of fungicides in greenhouse cultivation led to residual pollution in soils and then altered soil microbial community. However, it is unclear whether residual fungicides could affect the diversity and abundance of antibiotic resistance genes (ARGs) in greenhouse soils. Here, the dissipation of fungicides and its impact on the abundance of ARGs were determined using shotgun metagenomic sequencing in the greenhouse and mountain soils under laboratory conditions. Our results showed the greenhouse soils harbored more diverse and abundant ARGs than the mountain soils. The application of carbendazim, azoxystrobin, and chlorothalonil could increase the abundance of total ARGs in the greenhouse soils, especially for those dominant ARG subtypes including sul2, sul1, aadA, tet(L), tetA(G), and tetX2. The abundant ARGs were significantly correlated with mobile genetic elements (MGEs, e.g. intI1and R485) in the greenhouse soils but no significant relationship in the mountain soils. Meanwhile, the co-occurrence patterns of ARGs and MGEs, e.g., sul2 and R485, sul1 and transposase, were further verified via the genetic arrangement of genes on the metagenome-assembled contigs in the greenhouse soils. Additionally, host tracking analysis indicated that ARGs were mainly carried by enterobacteria in the greenhouse soils but actinomyces in the mountain soils. These findings confirmed that some fungicides might serve as the co-selectors of ARGs and elevated their abundance via MGEs-mediated horizontal gene transfer in the greenhouse soils.

Soils are the main reservoirs of POPs in mountain ecosystems, but the great variability of the concentrations, also at small scale, leaves some uncertainties in the evaluation of environmental burdens and exposure. The role of the aspect of the mountain side and the seasonal variation in the contamination levels was analysed by means of several soil samples taken from central Italian Alps. A greater contamination content was present in northern soils with a mean ratio between the north vs. south normalised concentration of around a factor of 2 (North–South Enrichment Factor). Experimental factors agreed with theoretical calculations based on temperature-specific calculated Ksa values. From May to November consistent differences in normalised concentrations up to 5-fold were observed. A dynamic picture of the POP contamination in high altitudinal soils is derived from the data in this work, with spring-summer half-lives between 60 and 120 days for most of the compounds. This paper discusses the accumulation of POPs in soils in relation to the aspect of the mountain side and supports the idea of a seasonal cycle of POPs in this matrix.

Soils are an important sink for persistent organic pollutants (POPs), and high mountain soils are considered a stable reservoir for many compounds due to their high organic matter content. This study focuses on the small-scale variability on the environmental distribution of dichlorodiphenyltrichloroethane (DDT) in mountain soils. Several soil samples taken from May 2007 to June 2008 in a small area at around 1,900 m a.s.l. (Italian Central Alps) were analyzed for DDT compounds. Pedological analyses were done as well. Organic matter content, soil layer, differences in solar radiation, and sampling period were considered as possible variability factors. Organic matter content can account for a DDT concentration difference of a factor 3 among different sites, soil layer can account for a concentration difference of a factor near 2, differences in solar radiation values do not seem to affect DDT concentrations, whereas the sampling period has the greatest influence with a difference factor of three to four among different sampling dates. Summing all these variability factors together, even though operating on such a small scale, we obtain a predicted spatial variability depending on the considered variables near to one order of magnitude. In particular, it was surprising that seasonal variations could be so great. If this conclusion is to be confirmed in the future, this element must be considered very carefully by scientists and environmental agencies during monitoring campaigns.

Polycyclic aromatic hydrocarbons (PAHs) were analyzed in 70 soils distributed in mountain areas such as Montseny (300–1,700 m), Pyrenees (1,500–2,900 m), Alps (1,100–2,500 m), and Tatras (1,400–1,960 m). Average total PAH concentrations, excluding retene and perylene, were about 400 ng/g in the Pyrenees and 1,300–1,600 ng/g in the other mountain ranges. No correlations between PAH concentrations and total organic carbon were observed. Retene was the major PAH in the Pyrenean soils of lower altitude. No altitudinal dependence was found between soil PAH concentrations and elevation for the whole dataset. However, in the Tatra soils a statistically significant correlation with altitude was observed involving higher concentrations at higher altitude. This correlation was due to the statistically significant altitudinal dependence of the more volatile PAHs. Another observed altitudinal trend concerned the benz[a]anthracene/(benz[a]anthracene + chrysene + triphenylene) and the benzo[a]pyrene/(benzo[a]pyrene + benzo[e]pyrene) ratios that exhibited a decrease in the more chemically labile compounds, benz[a]anthracene and benzo[a]pyrene, respectively, in the soils located at higher altitude. This observation is consistent with the expected higher photooxidation at higher mountain altitude.

POPs are still a priority environmental problem, but can be used as a scientific tool for understanding the distribution phenomena. Both high mountains and polar areas are seen as priority zones for contamination studies. In this context, two altitudinal series of soil samples were analysed for several classes of Persistent Organic Pollutants (PCBs, DDTs, HCHs, HCB and chlordane). Two transects were carried out - one in the Peruvian Andes (Cordillera Blanca) and the other in the Italian Alps (Mount Legnone). In these two areas, POP composition and levels both gave different results, linked to regional emission history. The Italian samples were characterized by high levels of industrial type compounds, and by surprisingly high DDT contamination, due to a defined consistent local source in Northern Italy. The Peruvian samples, on the other hand, were characterized by generally low POP levels with relatively high DDT contamination. The concentration increase in line with elevation was evident only in the Italian transect, where higher precipitation intensities and an increasingly higher precipitation gradient in accordance with altitude was found present. Precipitations are considered a key factor for enhancing the condensation effect at high altitudes and for reducing summer revolatilisation, as they lower soil temperature. In the Italian altitudinal gradient, evidence of fractionation processes, with a shift of the PCB composition towards less chlorinated congeners, and a vegetation effect with a mean woodland/grassland enrichment factor between 2 and 4 were also observed.

The research was carried out in the spruce forests of Barania Góra (Silesian Beskids, Poland) affected by pandemic dying of trees. Twenty-seven samples were collected from the O layer in two plots: 17 in a cut down forest infested with insect pests (bark beetle) and ten in a 120-year-old healthy forest. The analyses covered basic parameters (pHH2O, pHKCl, worg, Ctot, Ntot, CEC) and the concentrations of aluminium in the fractions leached with 0.1 M BaCl2 (Alexch), 0.5 M CuCl2 and 0.1 M Na4P2O7 (Albio) solutions. The total aluminium concentration in the soil was assayed digesting samples with hydrofluoric acid. The effect of pH and organic matter content on the amount of exchangeable (Alexch) and bioavailable (Alexch) aluminium in the soil was analysed. It has been found that the soils in both plots are strongly acidic and contain 550 to 1,700 mg kg−1 of exchangeable aluminium and 1,200 to 4,800 mg kg−1 of bioavailable aluminium. The lack of disease symptoms in the spruce trees in plot 2 can be explained by the higher content of organic matter in the soil. Unfortunately, one might expect that the high concentration of exchangeable aluminium will also cause the trees in the area to wither.

Background, aim, and scope High mountain soils constitute a long-term cumulative record of atmospherically deposited trace elements from both natural and anthropogenic sources. The main aims of this study were to determine the level of major and trace metals (Al, Ti, Mn, Fe, and Zr) of lithologic origin and airborne contaminating trace elements (Ni, Cu, Zn, As, Cd, and Pb) in soils in the Central Pyrenees as an indication of background contamination over SW Europe, to establish whether there is a spatial pattern of accumulation of trace elements in soils as a function of altitude, and to examine whether altitude-related physicochemical properties of soils affect the accumulation of major metals and trace elements. Methods Major metals and trace elements were measured in “top” (i.e., first 10 cm) and “bottom” (i.e., below 10 cm) soil samples along an altitudinal transect (1,520-2,880 m a.s.l.) in the Central Pyrenees. Total concentrations were determined by X-ray fluorescense spectrometry. Total major metal concentrations were analysed by conventional X-ray fluorescence spectrometry (XRF) with a Siemens SRS 303 instrument. Total trace element concentrations were determined with an energy-dispersive multielement miniprobe XRF analyser. Acid-extractable concentrations were measured by inductively coupled plasma after previous extraction with nitric acid and hydrogen peroxide in closed beakers. Acid-extractable major metal concentrations were measured by inductively coupled plasma (ICP)-Optic Emission Spectrometry with a Perkin Elmer 3200 RL Instrument. Acid-extractable trace element concentrations were determined by ICP-Mass Spectrometry with a Perkin Elmer ELAN 6000. Results Trace element concentration ranges were (in mg kg⁻¹, inventories in g m⁻² between parenthesis) <2-58 (0.5-6.6) for Ni, 6-30 (0.2-3.4) for Cu, 38-236 (1.6-32.4) for Zn, 6-209 (0.2-12.8) for As, 0.02-0.64 (<0.04) for Cd, and 28-94 (0.6-13.0) for Pb. These concentrations were, in general, comparable to those recorded in soils from other European mountainous areas and were in many cases above the threshold recommended for ecosystem protection by regional and European environmental authorities. The highest concentrations were found at lower altitudes, indicating an effect of local contamination up to ∼2,300 m a.s.l. Only above this altitude can trace elements in soils be considered representative of a background, long-range atmospheric contamination. Conclusions None of the storage capacity properties of soils examined were determinant of the differences in elemental concentrations along the altitudinal transect. At the upper altitude range, Ni, Cu, and Pb showed a approximately two- to fivefold increase over the average concentration of the local dominant lithology, reflecting the regional and global background of atmospheric contamination in the area.