Dr. Tume-Zapata, Pedro

Soil is a component of the environment. An environmental policy should identify the sources of trace metals in the soil and their effects on people and living beings. The concentrations of 29 surface soil samples (0–25 cm) were determined using the methods EPA 3050B. The data were analyzed using simple and robust statistical analysis that allowed for determining geochemical baseline values. Principal component and correlation analyses were performed, which, together with a spatial analysis, allowed us to distinguish between geogenic and anthropogenic sources. The degree of soil contamination was evaluated using different ecological indices, and the health risks to children and adults were calculated using formulas proposed by the United States Environmental Protection Agency (USEPA). The median concentrations of the analyzed elements correspond to Al 17,666 (mg/kg), As 8.7 (mg/kg), Ba 61.4 (mg/kg), Cd 0.17 (mg/kg), Cr 11.3 (mg/kg), Cu 20.5 (mg/kg), Fe 25,953 (mg/kg), Hg 0.06 (mg/kg), Mn 499 (mg/kg), Ni 20.8 (mg/kg), Pb 15.9 (mg/kg), and Zn 60.6 (mg/kg). In the principal component analysis, four factors were identified that explain 70.3% of the variability of the elements, which, together with the correlation analysis, suggest that the origin of the elements is mainly geogenic with some possible anthropic contributions. The elements analyzed in the soil with moderate contamination correspond to As, Cd, and Pb, in addition, As is the only element that indicated a value above the limit for carcinogenic risk in children. The estimated geochemical baseline values correspond to Al 34,734 (mg/kg), As 15.3 (mg/kg), Ba 113 (mg/kg), Cd 0.41 (mg/kg), Cr 33.8 (mg/kg), Cu 42.9 (mg/kg), Fe 46,181 (mg/kg), Hg 0.12 (mg/kg), Mn 1015 (mg/kg), Ni 42.2 (mg/kg), Pb 21.6 (mg/kg), and Zn 121 (mg/kg). 89.7% of the total samples are at a low level of contamination. The carcinogenic risk due to As in children represents 3.4% of the total samples, so it is considered insignificant.

Mining activity is one of the main sources to pollute soil, water and plants. An analysis of soil and plant samples around the Atrevida mining area in Catalonia (NE Spain) was preformed to determine potentially harmful elements (PHEs). Soil and plant samples were taken at eight locations around the mining area. The topsoil (0–15 cm) samples were analysed for physico-chemical properties by standard methods, by ICP-MS for Cd, Co, Cr, Cu, Fe, Ni, Pb and Zn, and were microwave-digested. Plant, root and shoot samples were digested separately, and heavy metals were analysed by AAS. Translocation factor (TF), biological concentration factor (BCF) and biological accumulation factor (BAF) were determined to assess the tolerance strategies developed by native species and to evaluate their potential for phytoremediation purposes. Soil pH was generally acid (5.48–6.72), with high soil organic matter (SOM) content and a sandy loamy or loamy texture. According to the agricultural soil values in southern Europe, our PHEs concentrations exceeded the toxicity thresholds. The highest root content of the most studied PHEs appeared in Thymus vulgaris L. and Festuca ovina L., while Biscutella laevigata L. accumulated more PHEs in shoots. The TF values were > 1 in B. laevigata L., but BAF obtained < 1, except Pb. B. laevigata L., and can be considered potentially useful for phytoremediation for having the capacity to restrict the accumulation of large PHEs amounts in roots and Pb translocation to shoots.

Urban areas are constantly growing. By 2050, the urban world population, it is predicted to reach 6 billion. Being component of cities environment, urban soils have elevated levels of potentially toxic elements from anthropogenic action. The aims of this study are (1) to establish background levels of potentially toxic element in soils in the city of Coronel and (2) to assess the pollution and identify its origin. Samples (129 in total) were collected in Coronel, from 43 sites in schoolyards. Three samples were taken at each site: 0–10 cm, 10–20 cm and 150 cm depth. Principal component analysis (PCA), cluster analysis (CA) and depth ratios were applied to distinguish the origin of the contamination. The geoaccumulation index, contamination factor and the integrated pollution index were used to estimate the pollution. The median concentration of the chemical elements in 0–10 cm depth was Ba 38 mg kg-1; Co 15 mg kg-1; Cr 18 mg kg-1; Cu 22 mg kg-1; Mn 536 mg kg-1; Ni 35.5 mg kg-1; Pb 6 mg kg-1; V 94 mg kg-1; Zn 65 mg kg-1. Principal component analysis and CA suggested that Co, Ni and Mn were mainly derived from geogenic origin, while Ba, Cr, Cu, Pb, V and Zn from anthropic origin. Contamination factor indicated that some soil samples were classified as considerable contaminated to very highly contaminated by Ba, Pb, Zn and V.

The specific objectives of this study were: (1) to establish background content levels of potentially harmful elements in topsoil of Quintero and Puchuncavi districts; (2) to assess the degree of topsoil pollution and identify the local sources of pollution; and (3) to assess the health risk of metal exposure to population. Data from a Chilean Environmental Ministry report were analyzed. Multivariate analysis suggests that the potentially harmful elements are split into two main groups, which can be explained by controlling geogenic (Ni, V and Zn) and anthropogenic (As, Cd, Cu and Pb) factors. The spatial distribution of As, Cd, Cu and Pb displays a spatial pattern around the Puchuncavi-Ventanas industrial park. The background values determined with MAD (median absolute deviation) method include As 31.6 mg kg-1, Cd 0.7 mg kg-1, Cu 296 mg kg-1, Ni 16.9 mg kg-1, Pb 48.6 mg kg-1, V 199 mg kg-1 and Zn 192 mg kg-1. The pollution indices reported considerable contamination to very high contamination in some soil samples. Hazard quotient values were higher for children than for adults, due to the ingestion and dermal absorption, while the cancer risk index values were in the acceptable range.

Anthropogenic activities often produce different emanations, some of them excessive, producing contamination of the soil, water, and/or air. This article analyzes soil conditions in Coronel, Chile, a commune with a large industrial presence, identifying the sources emitting potentially toxic elements, the degree of soil contamination, and the carcinogenic and non-carcinogenic risks in the area. Ninety-four samples in the study area were analyzed using different methods. Three factors were identified through a principal component analysis (PCA) that explain 83.27% of the variability of the elements. Four factors were identified through the positive matrix factorization (PMF) model, making it possible to identify the polluting sources according to the pattern of elements they contain. The sources of these factors were then identified. The most common elements in the soil with a particularly high degree of contamination are nickel, vanadium, and chromium, the latter of which being the element that poses the greatest carcinogenic and non-carcinogenic risk to children and adults. Additionally, the highest concentrations of chromium and vanadium were identified near industrial areas of the commune.

This preliminary study focuses on three abandoned sites, located in the communes of Temuco, Villarrica, and Lonquimay, in the Araucanía Region, Chile. Two of the sites were classified as illegal landfills and one was a former landfill. Seventy-three surface samples were taken, of which 32 were from site S1, 20 were from site S2, and 21 were from site S3. The objectives of this study were (1) to establish the background values of trace metals present in soils through different statistical methods, (2) to determine the level of contamination and possible ecological risks in soils, and (3) to assess the health risk posed to children and adults from potentially haz- ardous elements (As, Ba, Cd, Co, Cr, Cu, Hg, Ni, Pb, V, and Zn). The data analyzed belong toa report presented by Chile’s National Environmental Centre (CENMA). An evaluation was carried out through a multivariate statistical analysis to determine the type of origin and association of the trace elements, and spatial distribution maps were generated to establish the behavior of the contents of heavy metals present in the sites studied. The background values for sites S1, S2, and S3 were obtained by the median + 2MADdian absolute deviation) method. These values var- ied in the range of 14,702–41,785 mg kg−1 for Al, 0.83–8.9 mg kg−1 for As, 29.2–77.2 mg kg−1 for B, 59.2–143 mg kg−1 for Ba, 10.1–22.8 mg kg−1 for Cd, 18.4–51.2 mg kg−1 for Co, 12.3–38.0 mg kg−1 for Cr, 47.8–76.6 mg kg−1 for Cu, 36,230–64,274 mg kg−1 for Fe, 0.02–0.05 mg kg−1 for Hg, 482–4396 mg kg−1 for Mn, 16.7–19.3 mg kg−1 for Ni, 1.0–17.6 mg kg−1 for Pb, 1.4–28.2 mg kg−1 for Se, 108–258 mg kg−1 for V, and 68.1–145 mg kg−1 for Zn. In terms of ecological risk, the geoaccumu- lation index (Igeo), enrichment factor (EF), and contamination factor (Cf) values for As and Se at site S1, As at S2, and Pb with As at S3 were the main elements indicating the highest contamination levels, as well as a higher number of samples with contaminated content. The Potential Ecological Risk Index (PERI) revealed that on average, there was a moderate ecological risk for S1 and S2 and a considerable ecological risk for S3; the main contributions were generated by As and Hg in S1 and S2, while, in S3, they were produced by Pb and As. In terms of the risk to human health, the risk was higher in children than in adults, with the ingestion route as the main source of risk. For adults, it was found that there was no likelihood that they would develop any adverse non-carcinogenic or carcinogenic health effects. In contrast, children were found to be more likely to sustain adverse health effects. Regarding the non-carcinogenic risk to children, the Co and As samples at S1, S2, and S3, and the Pb at site S3 showed values exceeding the non-carcinogenic-risk limit. Regarding the carcinogenic risk, all three sites studied had Cd samples that indicated a likelihood of children developing cancer from this heavy metal.

In an annual monitoring in the Copiapó valley, the concentration of Cu, Hg, and As in sediments was related to environmental transfer processes, these elements also being present in surface water. The goal was to evaluate the uptake of the mentioned elements in wild plants of the Copiapó Valley, to determine if these species could be indicator plants to prevent environmental risks in local agriculture. From the same monitoring, the uptake of the elements was determined in wild plants growing near the irrigation channels; canopy of Tessaria absinthioides, Equisetum giganteum, Arundo donax, Melilotus indicus, Cortaderia rudiscula, and Sarcocornia neei was analyzed for the same elements. These plants were able to uptake Cu, Hg and As in concentration between 19 and 4674.5 times the environmental limits allowed for edible plants. This result shows that crop plants can also capture contaminants elements due to the frequency of irrigation. These plants can be used as indicators for the diagnosis of capture of the pollutants elements by plants and to prevent environmental hazards to human health in agricultural products from the Copiapó valley

The removal of copper ions, from synthetic solutions, using walnut shell and olive pomace waste as biosorbents was studied. Synthetic copper solutions were used, and the contact time, initial pH, biosorbent dose, and initial concentration of copper ions were evaluated. The used particle size of both biosorbents was inferior to 600 µm. In the elimination of copper ions, the walnut shell reached 88% (30 min), and the olive pomace 86.5% (40 min). The maximum removal of copper ions was at pH 5 with both biosorbents. The elimination of copper ions was constant with increasing doses of bio-sorbent; however, a decrease close to 90% in the biosorption capacity was determined, when the dose of biosorbent increased from 1 to 10 g/L. The effect of the biosorption capacity increased proportionally with the initial concentration of copper ions; achieving biosorption of 8.3 and 12.9 mg of Cu+2/g of biosorbent, with walnut shell and olive pomace, respectively. Both biosorbent allowed copper ions removal close to 90%; however, to the olive pomace was not necessary a size reduction and had a higher copper ions biosorption capacity than the walnut shell.

Attic dusts provide an indirect measure of airborne pollutants deposited in the urban environment. The objectives of this study are: (1) to determine the concentrations of As, Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr, V and Zn in attic dust in the City of Coronel, (2) to evaluate the source apportionment of PHE and (3) to assess the risk of health effects from exposure in adults and children. In the City of Coronel, attic dust samples were collected in 19 houses. The concentrations of As, Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr, V and Zn were measured in ICP-OES after Aqua Regia digestion of <75 µm dust sample. The median (and the range) concentration (mg kg−1) of potentially harmful elements was: As 16 (7–72), Ba 154 (53–251), Cd 0.8 (0.25–14.5), Co 12, (8–22),Cr 38 (22–482), Cu 107 (44–1641), Mn 698 (364–1245), Ni 51 (24–1734), Pb 66 (18–393), Sr 131 (52–252), V 129 (57–376) and Zn 815 (107–9761). The exploratory data analysis shows that Ni, Cu, Cr, Zn, Pb and As distribution is dominated by anthropogenic sources and characterized by high extreme values. Principal component analysis shows four factors. One factor is geogenic, while the other three factors are associated with transport emissions and the industrial park. The resulting median of cumulative noncarcinogenic risk (HIs) value for attic dust was 3.49 for children. This is significant, as any value greater than one indicates an elevated risk.

The objectives of this study are (a) to determine the background concentration of As, Cd, Cr, Hg and Pb in Arica commune; (b) to determine the degree of soil contamination in Arica city using environmental indices and (c) to evaluate the human health risk of these potentially toxic elements. In the rural area of Arica commune, 169 samples were taken and 283 samples were taken in the urban area of Arica city. Total concentrations of Cd, Pb and Cr were determined by EPA 3052 and EPA 6010 C. Mercury was determined by EPA 7473. Arsenic was determined by EPA 7061A. The available concentrations of As and Cr were determined by dilute hydrochloric acid and EPA 6010C. Environmental indices were applied for pollution and US EPA model was used to evaluate human health risk. Background concentrations were As 18.2, Cd 1.12, Cr 73.2, Hg 0.02 and Pb 11.8 mg kg−1, respectively. Environmental indices show that soil samples are located between slightly contaminated to extremely contaminated. Human health risk analysis shows that children have higher levels of risk than adults. The analysis with available concentrations of As and Cr shows no carcinogenic risk for adults and children, but 81% and 98% of the samples were between 10–6 and 10–4, that means intermediate risk.