12 research outputs found
Patterning total mercury distribution in coastal podzolic soils from an Atlantic area: influence of pedogenetic processes and soil components
Soils are the main Hg reservoir in the terrestrial ecosystems where it is deposited via wet or dry deposition and
litterfall. Once on the soil surface, different biogeochemical routes will determine the fate of Hg and the role of
terrestrial ecosystems as a Hg source or sink. The specific chemical and physical characteristics of Podzols and
podzolic soils contribute to the accumulation of Hg in their illuvial horizons, avoiding its leaching to groundwater.
The geographical location, state of pedogenesis, soil age, abundance of carrier phases and physical
properties can affect the presence and distribution of Hg in soils. Therefore, understand and relate these factors
with the behavior of Hg in Podzols and podzolic soils is key to define the role of this type of soil in the terrestrial
Hg cycle. In this work, ten podzolic soil profiles were collected in an Atlantic coastal forest area of Portugal and
analyzed for the main physico-chemical properties and Hg content to assess the influence of the intensity of
podzolization in the Hg depth distribution. Three different patterns of Hg distribution in the studied Podzols,
depending on the predominance of atmospheric deposition or the intensity of podzolization, have been defined.
The pattern I showed the maximum Hg contents in the surface A horizons (12.9–23.5 μg kg 1), pattern II
exhibited the highest peaks in the subsurface illuvial horizons (2.3–17.3 μg kg 1) and pattern III presented an
even distribution of Hg through the soil profile. We found that dissolved organic matter (DOM) is the main
carrier of Hg in the A and E horizons, whereas metal(Al, Fe)-humus complexes and/or oxyhydroxides contribute
to immobilizing Hg in the illuvial horizons (Bh, Bs and Bhs). The principal component regression (PCR) analysis
predicted satisfactorily the Hg distribution through soil organic matter and Al and Fe oxyhydroxides. The Hg
immobilized in the subsurface layers of Podzols is retained in the long term, avoiding its migration to other
components of terrestrial ecosystems where it could cause serious environmental damage such as groundwater
and superficial watersinfo:eu-repo/semantics/publishedVersio
Spread of a SARS-CoV-2 variant through Europe in the summer of 2020.
Following its emergence in late 2019, the spread of SARS-CoV-21,2 has been tracked by phylogenetic analysis of viral genome sequences in unprecedented detail3–5. Although the virus spread globally in early 2020 before borders closed, intercontinental travel has since been greatly reduced. However, travel within Europe resumed in the summer of 2020. Here we report on a SARS-CoV-2 variant, 20E (EU1), that was identified in Spain in early summer 2020 and subsequently spread across Europe. We find no evidence that this variant has increased transmissibility, but instead demonstrate how rising incidence in Spain, resumption of travel, and lack of effective screening and containment may explain the variant’s success. Despite travel restrictions, we estimate that 20E (EU1) was introduced hundreds of times to European countries by summertime travellers, which is likely to have undermined local efforts to minimize infection with SARS-CoV-2. Our results illustrate how a variant can rapidly become dominant even in the absence of a substantial transmission advantage in favourable epidemiological settings. Genomic surveillance is critical for understanding how travel can affect transmission of SARS-CoV-2, and thus for informing future containment strategies as travel resumes. © 2021, The Author(s), under exclusive licence to Springer Nature Limited
Pine bark as bio-adsorbent for Cd, Cu, Ni, Pb and Zn:batch-type and stirred flow chamber experiments
Degradation of sulfadiazine, sulfachloropyridazine and sulfamethazine in aqueous media
Antibiotics discharged to the environment constitute a main concern for which different treatment alternatives are being studied, some of them based on antibiotics removal or inactivation using by-products with adsorbent capacity, or which can act as catalyst for photo-degradation. But a preliminary step is to determine the general characteristics and magnitude of the degradation process effectively acting on antibiotics. A specific case is that of sulfonamides (SAs), one of the antibiotic groups most widely used in veterinary medicine, and which are considered the most mobile antibiotics, causing that they are frequently detected in both surface- and ground-waters, facilitating their entry in the food chain and causing public health hazards. In this work we investigated abiotic and biotic degradation of three sulfonamides (sulfadiazine –SDZ-, sulfachloropyridazine –SCP-, and sulfamethazine –SMT-) in aqueous media. The results indicated that, in filtered milliQ water and under simulated sunlight, the degradation sequence was: SCP > SDZ ≈ SMT. Furthermore, the rate of degradation clearly increased with the raise of pH: at pH 4.0, half-lives were 1.2, 70.5 and 84.4 h for SCP, SDZ and SMT, respectively, while at pH 7.2 they were 2.3, 9.4 and 13.2 h for SCP, SMT and SDZ. The addition of a culture medium hardly caused any change in degradation rates as compared to experiments performed in milliQ water at the same pH value (7.2), suggesting that in this case sulfonamides degradation rate was not affected by the presence of some chemical elements and compounds, such as sodium, chloride and phosphate. However, the addition of bacterial suspensions extracted from a soil and from poultry manure increased the rate of degradation of these antibiotics. This increase in degradation cannot be attributed to biodegradation, since there was no degradation in the dark during the time of the experiment (72 h). This indicates that photo-degradation constitutes the main removal mechanism for SAs in aqueous media, a mechanism that in this case was favored by humic acids supplied with the extracts from soil and manure. The overall results could contribute to the understanding of the environmental fate of the three sulfonamides studied, aiding to program actions that could favor their inactivation, which is especially relevant since its dissemination can involve serious environmental and public health risks.This work was supported by the Spanish Ministry of Economy and Competitiveness, with FEDER funds [grant numbers CGL2015-67333-C2-1-R and CGL2015-67333-C2-2-R]. M. Conde-Cid holds a pre-doctoral FPU contract (Ministry of Education, Culture and Sports, Spain). D. Fernández-Calviño holds a Ramon y Cajal contract (Ministry of Economy, Industry and Competitiveness, Spain). The sponsor had not involvement in study design; in the collection, analysis and interpretation of data; in the writing of the report, and in the decision to submit the article for publication
Biotic and abiotic dissipation of tetracyclines using simulated sunlight and in the dark
Veterinary antibiotics reaching soils and water bodies are considered emerging pollutants deserving special attention. In this work, dissipation of tetracycline (TC), oxytetracycline (OTC) and chlortetracycline (CTC) is investigated. Dissipation experiments in filtered water, using simulated sunlight, resulted in the following degradation sequence: TC < OTC ≈ CTC, with half-life values of 229, 101 and 104 min, respectively; however, no dissipation took place in the dark. Dissipation of the three tetracyclines in culture medium and with simulated sunlight was much higher, giving the sequence TC ≈ OTC < CTC, with half-lives of 9, 10 and 7 min, respectively; in the dark, TC and OTC did not suffer dissipation, but it was around 28% for CTC at the end of the experiment (480 min). The variable explaining a higher dissipation in culture medium and with light was pH, as this parameter caused changes in the distribution of species of tetracyclines, affecting degradation. Adding bacterial suspensions extracted from soil and poultry manure increased dissipation, giving the sequence: TC ≈ OTC < CTC, which is attributed to the presence of humic acids, which adsorb these antibiotics. These results could facilitate understanding the fate of antibiotics reaching environmental compartments and causing public health hazards.This work was supported by the Spanish Ministry of Economy and Competitiveness, with FEDER funds [grant numbers CGL2015-67333-C2-1-R and CGL2015-67333-C2-2-R]. M. Conde-Cid holds a pre-doctoral FPU contract (Ministry of Education, Culture and Sports). D. Fernández-Calviño holds a Ramon y Cajal contract (Ministry of Economy, Industry and Competitiveness). The sponsor had not involvement in study design; in the collection, analysis and interpretation of data; in the writing of the report, and in the decision to submit the article for publication