Pub Date : 2022-04-21DOI: 10.3390/pollutants2020012
Siavash Shami, Babak Ranjgar, Jinhu Bian, M. Khoshlahjeh Azar, Armin Moghimi, M. Amani, Amin Naboureh
The first case of COVID-19 in Iran was reported on 19 February 2020, 1 month before the Nowruz holidays coincided with the global pandemic, leading to quarantine and lockdown. Many studies have shown that environmental pollutants were drastically reduced with the spread of this disease and the decline in industrial activities. Among these pollutants, nitrogen dioxide (NO2) and carbon monoxide (CO) are widely caused by anthropogenic and industrial activities. In this study, the changes in these pollutants in Iran and its four metropolises (i.e., Tehran, Mashhad, Isfahan, and Tabriz) in three periods from 11 March to 8 April 2019, 2020, and 2021 were investigated. To this end, timeseries of the Sentinel-5P TROPOMI and in situ data within the Google Earth Engine (GEE) cloud-based platform were employed. It was observed that the results of the NO2 derived from Sentinel-5P were in agreement with the in situ data acquired from ground-based stations (average correlation coefficient = 0.7). Moreover, the results showed that the concentration of NO2 and CO pollutants in 2020 (the first year of the COVID-19 pandemic) was 5% lower than in 2019, indicating the observance of quarantine rules, as well as people’s initial fear of the coronavirus. Contrarily, these pollutants in 2021 (the second year of the COVID-19 pandemic) were higher than those in 2020 by 5%, which could have been due to high vehicle traffic and a lack of serious policy- and law-making by the government to ban urban and interurban traffic. These findings are essential criteria that might be used to guide future manufacturing logistics, traffic planning and management, and environmental sustainability policies and plans. Furthermore, using the COVID-19 scenario and free satellite-derived data, it is now possible to investigate how harmful gas emissions influence air quality. These findings may also be helpful in making future strategic decisions on how to cope with the virus spread and lessen its negative social and economic consequences.
{"title":"Trends of CO and NO2 Pollutants in Iran during COVID-19 Pandemic Using Timeseries Sentinel-5 Images in Google Earth Engine","authors":"Siavash Shami, Babak Ranjgar, Jinhu Bian, M. Khoshlahjeh Azar, Armin Moghimi, M. Amani, Amin Naboureh","doi":"10.3390/pollutants2020012","DOIUrl":"https://doi.org/10.3390/pollutants2020012","url":null,"abstract":"The first case of COVID-19 in Iran was reported on 19 February 2020, 1 month before the Nowruz holidays coincided with the global pandemic, leading to quarantine and lockdown. Many studies have shown that environmental pollutants were drastically reduced with the spread of this disease and the decline in industrial activities. Among these pollutants, nitrogen dioxide (NO2) and carbon monoxide (CO) are widely caused by anthropogenic and industrial activities. In this study, the changes in these pollutants in Iran and its four metropolises (i.e., Tehran, Mashhad, Isfahan, and Tabriz) in three periods from 11 March to 8 April 2019, 2020, and 2021 were investigated. To this end, timeseries of the Sentinel-5P TROPOMI and in situ data within the Google Earth Engine (GEE) cloud-based platform were employed. It was observed that the results of the NO2 derived from Sentinel-5P were in agreement with the in situ data acquired from ground-based stations (average correlation coefficient = 0.7). Moreover, the results showed that the concentration of NO2 and CO pollutants in 2020 (the first year of the COVID-19 pandemic) was 5% lower than in 2019, indicating the observance of quarantine rules, as well as people’s initial fear of the coronavirus. Contrarily, these pollutants in 2021 (the second year of the COVID-19 pandemic) were higher than those in 2020 by 5%, which could have been due to high vehicle traffic and a lack of serious policy- and law-making by the government to ban urban and interurban traffic. These findings are essential criteria that might be used to guide future manufacturing logistics, traffic planning and management, and environmental sustainability policies and plans. Furthermore, using the COVID-19 scenario and free satellite-derived data, it is now possible to investigate how harmful gas emissions influence air quality. These findings may also be helpful in making future strategic decisions on how to cope with the virus spread and lessen its negative social and economic consequences.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84462879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-04-08DOI: 10.3390/pollutants2020011
G. Giacosa, C. Barnett, D. Rainham, T. Walker
The pulp and paper industry is a major contributor to water and air pollution globally. Pulp and paper processing is an intensive energy consuming process that produces multiple contaminants that pollute water, air, and affect ecological and human health. In Canada, the National Pollutant Release Inventory (NPRI) is used to assess the release of air pollutants into the atmosphere from industrial facilities (including pulp and paper mills) and provides a repository of annual emissions reported by individual facilities. This study compared annual air emissions of carbon monoxide, nitrogen oxides, total particulate matter (TPM), PM2.5, PM10, sulphur dioxide, and volatile organic compounds from nine different pulp and/or paper mills in Atlantic Canada from three provinces (Nova Scotia, New Brunswick, and Newfoundland and Labrador) between 2002 and 2019. Results revealed that annual releases were several orders of magnitude higher than federal reporting thresholds suggested by Environment and Climate Change Canada. Pulp mills emit higher pollutant loads than those producing paper. The highest exceedance of a reporting threshold was for particulate matter (PM2.5) at Northern Pulp in Nova Scotia. The emissions of PM2.5 were on average (over a 17-year period) about 100,000% above the reporting threshold of 0.3 tonnes per year.
{"title":"Characterization of Annual Air Emissions Reported by Pulp and Paper Mills in Atlantic Canada","authors":"G. Giacosa, C. Barnett, D. Rainham, T. Walker","doi":"10.3390/pollutants2020011","DOIUrl":"https://doi.org/10.3390/pollutants2020011","url":null,"abstract":"The pulp and paper industry is a major contributor to water and air pollution globally. Pulp and paper processing is an intensive energy consuming process that produces multiple contaminants that pollute water, air, and affect ecological and human health. In Canada, the National Pollutant Release Inventory (NPRI) is used to assess the release of air pollutants into the atmosphere from industrial facilities (including pulp and paper mills) and provides a repository of annual emissions reported by individual facilities. This study compared annual air emissions of carbon monoxide, nitrogen oxides, total particulate matter (TPM), PM2.5, PM10, sulphur dioxide, and volatile organic compounds from nine different pulp and/or paper mills in Atlantic Canada from three provinces (Nova Scotia, New Brunswick, and Newfoundland and Labrador) between 2002 and 2019. Results revealed that annual releases were several orders of magnitude higher than federal reporting thresholds suggested by Environment and Climate Change Canada. Pulp mills emit higher pollutant loads than those producing paper. The highest exceedance of a reporting threshold was for particulate matter (PM2.5) at Northern Pulp in Nova Scotia. The emissions of PM2.5 were on average (over a 17-year period) about 100,000% above the reporting threshold of 0.3 tonnes per year.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84615006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-04-06DOI: 10.3390/pollutants2020010
Yicheng Zeng, Aurélie Laguerre, Elliott T. Gall, Mohammad Heidarinejad, B. Stephens
Electronic air cleaning (EAC) technologies have garnered significant attention for use in buildings. Many EAC technologies rely on the addition of reactive constituents to indoor air to react with gas-phase compounds, enhance particle deposition, and/or inactivate microorganisms. However, limited data are available on the efficacy of many EAC technologies and their potential to form chemical byproducts during operation. Here we experimentally evaluate the indoor air quality impacts, specifically targeting particles and gases but not microbial constituents, of a commercially available additive oxidizing EAC that generates positive and negative ions and hydrogen peroxide (H2O2). Tests were conducted in a large unoccupied test chamber in Chicago, IL and an unoccupied laboratory in Portland, OR under a combination of natural conditions (i.e., without pollutant injection) and perturbation conditions (i.e., with pollutant injection and decay). A combination of integrated and time-resolved measurements was used across both test locations. Chamber tests at lower airflow rates demonstrated that operation of the EAC: (i) had no discernible impact on particle concentrations or particle loss rates, with estimated clean air delivery rates (CADRs) for various particle measures less than ±10 m3/h, (ii) was associated with apparent decreases in some volatile organic compounds (VOCs) and increases in other VOCs and aldehydes, especially acetaldehyde, although a combination of high propagated uncertainty, limitations in test methods (e.g., lack of replicates), and variability between repeated tests limit what quantitative conclusions can be drawn regarding gas-phase organics; (iii) did generate H2O2, assessed using a crude measure, and (iv) did not generate ozone (O3). Laboratory tests at higher airflow rates, which involved injection and decay of particles and a single VOC (limonene), both simultaneously and separately, demonstrated that: (i) pollutant loss rates for both particles and limonene were slightly lower with the EAC on compared to off, yielding slightly negative pollutant removal efficiencies (albeit largely within propagated uncertainty) and (ii) there was a change in observed concentrations of one potential limonene degradation product, m/z 59 (putatively identified as acetone), with steady-state levels increasing from 10 ppb (air cleaner off) to 15 ppb (air cleaner on). No increases or decreases beyond measurement uncertainty were observed for other analyzed gaseous limonene degradation products. Overall, both chamber and laboratory tests demonstrated negligible effectiveness of this device at the test conditions described herein for removing particles and mixed results for VOCs, including decreases in some VOCs, no discernible differences in other VOCs, and apparent increases in other compounds, especially lower molecular weight aldehydes including acetaldehyde.
{"title":"Experimental Evaluations of the Impact of an Additive Oxidizing Electronic Air Cleaner on Particles and Gases","authors":"Yicheng Zeng, Aurélie Laguerre, Elliott T. Gall, Mohammad Heidarinejad, B. Stephens","doi":"10.3390/pollutants2020010","DOIUrl":"https://doi.org/10.3390/pollutants2020010","url":null,"abstract":"Electronic air cleaning (EAC) technologies have garnered significant attention for use in buildings. Many EAC technologies rely on the addition of reactive constituents to indoor air to react with gas-phase compounds, enhance particle deposition, and/or inactivate microorganisms. However, limited data are available on the efficacy of many EAC technologies and their potential to form chemical byproducts during operation. Here we experimentally evaluate the indoor air quality impacts, specifically targeting particles and gases but not microbial constituents, of a commercially available additive oxidizing EAC that generates positive and negative ions and hydrogen peroxide (H2O2). Tests were conducted in a large unoccupied test chamber in Chicago, IL and an unoccupied laboratory in Portland, OR under a combination of natural conditions (i.e., without pollutant injection) and perturbation conditions (i.e., with pollutant injection and decay). A combination of integrated and time-resolved measurements was used across both test locations. Chamber tests at lower airflow rates demonstrated that operation of the EAC: (i) had no discernible impact on particle concentrations or particle loss rates, with estimated clean air delivery rates (CADRs) for various particle measures less than ±10 m3/h, (ii) was associated with apparent decreases in some volatile organic compounds (VOCs) and increases in other VOCs and aldehydes, especially acetaldehyde, although a combination of high propagated uncertainty, limitations in test methods (e.g., lack of replicates), and variability between repeated tests limit what quantitative conclusions can be drawn regarding gas-phase organics; (iii) did generate H2O2, assessed using a crude measure, and (iv) did not generate ozone (O3). Laboratory tests at higher airflow rates, which involved injection and decay of particles and a single VOC (limonene), both simultaneously and separately, demonstrated that: (i) pollutant loss rates for both particles and limonene were slightly lower with the EAC on compared to off, yielding slightly negative pollutant removal efficiencies (albeit largely within propagated uncertainty) and (ii) there was a change in observed concentrations of one potential limonene degradation product, m/z 59 (putatively identified as acetone), with steady-state levels increasing from 10 ppb (air cleaner off) to 15 ppb (air cleaner on). No increases or decreases beyond measurement uncertainty were observed for other analyzed gaseous limonene degradation products. Overall, both chamber and laboratory tests demonstrated negligible effectiveness of this device at the test conditions described herein for removing particles and mixed results for VOCs, including decreases in some VOCs, no discernible differences in other VOCs, and apparent increases in other compounds, especially lower molecular weight aldehydes including acetaldehyde.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83984614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-01DOI: 10.3390/pollutants2010008
Diogo Trajano Gomes da Silva, J. Ebdon, D. Dancer, C. Baker-Austin, H. Taylor
Sewage pollution leads to the contamination of bivalve shellfish by pathogenic microorganisms. Bacterial indicators support the management of risks associated with the consumption of shellfish; however, they often fail to indicate adequately the potential hazard to human health posed by certain human enteric viruses. Bacteriophages have been proposed as alternative indicators that may more effectively predict the presence of enteric viral pathogens. This study explored the relationships between bacterial indicators (Escherichia coli (E. coli), faecal coliforms (FC) and intestinal enterococci (IE)), phages (somatic (SOMPH), F-specific RNA (F + PH) and human-specific Bacteroides GB-124 phages (GB124PH)) and Norovirus (NoV) (GI/GII) in mussels (Mytilus edulis) and their overlying waters. The bioaccumulation of these indicators and Norovirus in shellfish matrices (e.g., flesh, digestive gland) was investigated bimonthly over a 12-month period in an English estuary. The findings revealed a marked seasonality in the distribution of all organisms, with the highest levels occurring during the autumn/winter months. The levels of all phages in shellfish and their overlying waters correlated better with the levels of Norovirus than with those of bacterial indicators. Somatic coliphages were the indicator that exhibited the strongest correlations with NoV (rho = 0.929). This study suggests that relatively low-cost culture-based phage enumeration appears to offer a more accurate indication of the likely presence of Norovirus in mussels than traditional bacterial indicators.
{"title":"A Longitudinal Study of Bacteriophages as Indicators of Norovirus Contamination of Mussels (Mytilus edulis) and Their Overlying Waters","authors":"Diogo Trajano Gomes da Silva, J. Ebdon, D. Dancer, C. Baker-Austin, H. Taylor","doi":"10.3390/pollutants2010008","DOIUrl":"https://doi.org/10.3390/pollutants2010008","url":null,"abstract":"Sewage pollution leads to the contamination of bivalve shellfish by pathogenic microorganisms. Bacterial indicators support the management of risks associated with the consumption of shellfish; however, they often fail to indicate adequately the potential hazard to human health posed by certain human enteric viruses. Bacteriophages have been proposed as alternative indicators that may more effectively predict the presence of enteric viral pathogens. This study explored the relationships between bacterial indicators (Escherichia coli (E. coli), faecal coliforms (FC) and intestinal enterococci (IE)), phages (somatic (SOMPH), F-specific RNA (F + PH) and human-specific Bacteroides GB-124 phages (GB124PH)) and Norovirus (NoV) (GI/GII) in mussels (Mytilus edulis) and their overlying waters. The bioaccumulation of these indicators and Norovirus in shellfish matrices (e.g., flesh, digestive gland) was investigated bimonthly over a 12-month period in an English estuary. The findings revealed a marked seasonality in the distribution of all organisms, with the highest levels occurring during the autumn/winter months. The levels of all phages in shellfish and their overlying waters correlated better with the levels of Norovirus than with those of bacterial indicators. Somatic coliphages were the indicator that exhibited the strongest correlations with NoV (rho = 0.929). This study suggests that relatively low-cost culture-based phage enumeration appears to offer a more accurate indication of the likely presence of Norovirus in mussels than traditional bacterial indicators.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81331050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-01DOI: 10.3390/pollutants2010007
Ali Daryabeigi Zand, Karl H. Mühling
Copper is a frequently used heavy metal worldwide and known to be an essential micronutrient for most living organisms including plants. However, excessive levels of copper in soil may adversely affect plant growth and survival. The continuing introduction of copper to soil, e.g., through excessive utilization of agrochemicals has raised serious environmental concerns throughout the world. A variety of plants have the capability to eliminate pollutants from soil through different mechanisms; however, limited information is reported on phytoremediation potential of maize (Zea mays L.) and its uptake and the accumulation potential in copper-containing soils. The effects of additions of 0, 50, 100, 200 and 300 mg kg−1 of copper to soil on growth parameters of Z. mays, copper uptake from soil and accumulation in roots and shoots, and phytoremediation potential of Z. mays were investigated in this research. Copper content in soil and plant samples were determined using atomic absorption spectrophotometry. The addition of 50 mg kg−1 Cu stimulated Z. mays growth parameters, while higher content of Cu exhibited inhibitory effects of plant growth. Results indicated that roots accumulated significantly higher levels of Cu than shoots in all treatments, suggesting dominancy of phytostabilization mechanism in remediation of Cu-polluted soil by Z. mays. However, translocation of Cu from the roots to the aerial parts enhanced to some extent with copper level in soil. The greatest Cu accumulation capacity of 5210 µg per pot was gained in Z. mays cultivated in soil treated with 200 mg kg−1 copper. Results demonstrated that Z. mays can promisingly remediate low to moderately copper-contaminated soils.
铜是世界范围内常用的重金属，是包括植物在内的大多数生物必需的微量营养素。然而，土壤中铜含量过高可能会对植物的生长和存活产生不利影响。继续向土壤中引入铜，例如通过过度使用农用化学品，在全世界引起了严重的环境问题。多种植物具有通过不同机制清除土壤污染物的能力;然而，关于玉米(Zea mays L.)的植物修复潜力及其在含铜土壤中的吸收和积累潜力的报道有限。研究了土壤添加0、50、100、200和300 mg kg - 1铜对柽柳生长参数、根、梢对土壤铜的吸收和积累以及柽柳植物修复潜力的影响。采用原子吸收分光光度法测定了土壤和植物样品中的铜含量。添加50 mg kg−1 Cu刺激了Z. mays的生长参数，而较高Cu含量则表现出抑制植物生长的作用。结果表明，在不同处理下，根的Cu积累量均显著高于茎，表明紫苏修复铜污染土壤的植物稳定机制占主导地位。但随着土壤中铜含量的增加，铜从根部向地上部分的转运有一定程度的增强。在200 mg kg - 1铜处理的土壤中，青梅的铜累积量最大，为5210µg /盆。结果表明，青霉对低、中度铜污染土壤具有良好的修复作用。
{"title":"Phytoremediation Capability and Copper Uptake of Maize (Zea mays L.) in Copper Contaminated Soils","authors":"Ali Daryabeigi Zand, Karl H. Mühling","doi":"10.3390/pollutants2010007","DOIUrl":"https://doi.org/10.3390/pollutants2010007","url":null,"abstract":"Copper is a frequently used heavy metal worldwide and known to be an essential micronutrient for most living organisms including plants. However, excessive levels of copper in soil may adversely affect plant growth and survival. The continuing introduction of copper to soil, e.g., through excessive utilization of agrochemicals has raised serious environmental concerns throughout the world. A variety of plants have the capability to eliminate pollutants from soil through different mechanisms; however, limited information is reported on phytoremediation potential of maize (Zea mays L.) and its uptake and the accumulation potential in copper-containing soils. The effects of additions of 0, 50, 100, 200 and 300 mg kg−1 of copper to soil on growth parameters of Z. mays, copper uptake from soil and accumulation in roots and shoots, and phytoremediation potential of Z. mays were investigated in this research. Copper content in soil and plant samples were determined using atomic absorption spectrophotometry. The addition of 50 mg kg−1 Cu stimulated Z. mays growth parameters, while higher content of Cu exhibited inhibitory effects of plant growth. Results indicated that roots accumulated significantly higher levels of Cu than shoots in all treatments, suggesting dominancy of phytostabilization mechanism in remediation of Cu-polluted soil by Z. mays. However, translocation of Cu from the roots to the aerial parts enhanced to some extent with copper level in soil. The greatest Cu accumulation capacity of 5210 µg per pot was gained in Z. mays cultivated in soil treated with 200 mg kg−1 copper. Results demonstrated that Z. mays can promisingly remediate low to moderately copper-contaminated soils.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81930754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-11DOI: 10.3390/pollutants2010006
Pedro Fraga-Santiago, Sofia Dias, Cristiana Silva, C. Gomes, C. Almeida
The aim of the present work was to evaluate the influence of two different pharmaceutical compounds (bezafibrate and paroxetine) on the phytoremediation potential of Phragmites australis in an estuarine medium contaminated by copper. Plants were exposed for seven days to a simplified estuarine medium, elutriate solution, with or without sediment. The medium was doped with copper and bezafibrate or paroxetine. P. australis plants were able to accumulate a significant amount of Cu, particularly in their roots (600 and 250 times increase in copper levels in the absence and presence of sediment, respectively), corroborating the phytostabilization potential of salt marsh plants. Metal uptake and translocation was significantly lower in the presence of sediment (Cu in leaves increased 20 times in the absence and only 4 times in the presence of sediment). An effect of either pharmaceutical compound on metal accumulation was not observed (levels of Cu in plants tissues were in general identical) but, in the presence of sediment, both bezafibrate and paroxetine changed Cu solubility in elutriate solution, either decreasing or increasing it. The current study highlights the possible influence the presence of contaminants of different characteristics (inorganic and organic contaminants) can have on salt marsh phytoremediation potential in the long run, and the effects pollutants might have in the environment.
{"title":"Pharmaceuticals Influence on Phragmites australis Phytoremediation Potential in Cu Contaminated Estuarine Media","authors":"Pedro Fraga-Santiago, Sofia Dias, Cristiana Silva, C. Gomes, C. Almeida","doi":"10.3390/pollutants2010006","DOIUrl":"https://doi.org/10.3390/pollutants2010006","url":null,"abstract":"The aim of the present work was to evaluate the influence of two different pharmaceutical compounds (bezafibrate and paroxetine) on the phytoremediation potential of Phragmites australis in an estuarine medium contaminated by copper. Plants were exposed for seven days to a simplified estuarine medium, elutriate solution, with or without sediment. The medium was doped with copper and bezafibrate or paroxetine. P. australis plants were able to accumulate a significant amount of Cu, particularly in their roots (600 and 250 times increase in copper levels in the absence and presence of sediment, respectively), corroborating the phytostabilization potential of salt marsh plants. Metal uptake and translocation was significantly lower in the presence of sediment (Cu in leaves increased 20 times in the absence and only 4 times in the presence of sediment). An effect of either pharmaceutical compound on metal accumulation was not observed (levels of Cu in plants tissues were in general identical) but, in the presence of sediment, both bezafibrate and paroxetine changed Cu solubility in elutriate solution, either decreasing or increasing it. The current study highlights the possible influence the presence of contaminants of different characteristics (inorganic and organic contaminants) can have on salt marsh phytoremediation potential in the long run, and the effects pollutants might have in the environment.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80559433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-08DOI: 10.3390/pollutants2010005
B. Yadav, P. Gupta
The use of conventional techniques for physico-chemical remediation of hydrocarbon such non-aqueous phase liquids (NAPL)-polluted sites may disturb the natural biotic settings of the (sub)-surface. However, natural attenuation has been reported very slow and sometime results as incomplete removal under prevailing site conditions. In particular, microbial growth is quite slow in cold regions, which reduces the applicability of bioremediation in treating NAPL-polluted soil-water. Thus, this study aims to evaluate the thermally enhanced bioremediation techniques to treat NAPL-polluted soil-water using practical experiments. A one-dimensional large column setup was designed and fabricated for this purpose. The column was integrated with automatic temperature controlling baths to maintain different soil-water temperatures (4 °C, 20 °C, 28 °C, and 36 °C), which was circulated through the porous media filled in the column setup. Results show a high dissolution rate of toluene, the selected light NAPL, at an elevated temperature of 28–36 °C. The biodegradation rates of the NAPL were found to be 0.002 mg L/h, 0.008 mg L/h, 0.012 mg L/h, and 0.015 mg L/h at soil-water temperature levels of 4 °C, 20 °C, 28 °C, and 36 °C, respectively. It was found that at high soil-water temperature (28 °C and 36 °C), a significant increment in microbial actions accelerates the biodegradation rate of NAPL in the subsurface system. The outcomes of this study may help in treating NAPL-polluted sites using solar or geo-thermal based heating systems for thermally enhanced bioremediation.
{"title":"Thermally Enhanced Bioremediation of NAPL Polluted Soil-Water Resources","authors":"B. Yadav, P. Gupta","doi":"10.3390/pollutants2010005","DOIUrl":"https://doi.org/10.3390/pollutants2010005","url":null,"abstract":"The use of conventional techniques for physico-chemical remediation of hydrocarbon such non-aqueous phase liquids (NAPL)-polluted sites may disturb the natural biotic settings of the (sub)-surface. However, natural attenuation has been reported very slow and sometime results as incomplete removal under prevailing site conditions. In particular, microbial growth is quite slow in cold regions, which reduces the applicability of bioremediation in treating NAPL-polluted soil-water. Thus, this study aims to evaluate the thermally enhanced bioremediation techniques to treat NAPL-polluted soil-water using practical experiments. A one-dimensional large column setup was designed and fabricated for this purpose. The column was integrated with automatic temperature controlling baths to maintain different soil-water temperatures (4 °C, 20 °C, 28 °C, and 36 °C), which was circulated through the porous media filled in the column setup. Results show a high dissolution rate of toluene, the selected light NAPL, at an elevated temperature of 28–36 °C. The biodegradation rates of the NAPL were found to be 0.002 mg L/h, 0.008 mg L/h, 0.012 mg L/h, and 0.015 mg L/h at soil-water temperature levels of 4 °C, 20 °C, 28 °C, and 36 °C, respectively. It was found that at high soil-water temperature (28 °C and 36 °C), a significant increment in microbial actions accelerates the biodegradation rate of NAPL in the subsurface system. The outcomes of this study may help in treating NAPL-polluted sites using solar or geo-thermal based heating systems for thermally enhanced bioremediation.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84809684","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-04DOI: 10.3390/pollutants2010004
Fanny Clergeaud, S. Fagervold, A. Rodrigues, Evane Thorel, D. Stien, P. Lebaron
Organic UV filters are continuously released in aquatic ecosystems due to their widespread use, especially in touristic coastal environments. Generally, organic UV filters are poorly soluble in water and tend to accumulate in the sediment compartment. This represents a conceivable risk for sediment-dwelling organisms and a potential for transfer of the UV filters up the food chain. This study aimed to assess the potential transfer of seven UV filters including benzophenone-3 (BP3), bis-ethylhexyloxyphenol methoxyphenyl triazine (BEMT), butyl methoxydibenzoylmethane (BM), methylene bis-benzotriazolyl tetramethylbutylphenol (MBBT), 2-ethylhexyl salicylate (ES), diethylhexyl butamido triazone (DBT), and octocrylene (OC) from artificial spiked sediment (10 µg·g−1 dry weight) to sediment-dwelling worms. All UV filters were detected in the worms after 28 days of exposure, but only BP3 was apparently bioaccumulated, with a biota sediment accumulation factor (BSAF) of 12.38 ± 4.65. However, metabolomic profiling revealed that OC was metabolized by the worms into 11 fatty acid conjugates, demonstrating that OC did also accumulate in the worms in the form of OC–fatty acid conjugates. Here, the sole quantification of the parent organic UV filter underestimated the accumulation factor and the exposure of organisms. In general, it is therefore important to pair the conventional method (BSAF calculus) with other techniques, such as metabolomics, to assess the actual potential for bioaccumulation of xenobiotics including transformed xenobiotics.
{"title":"Transfer of 7 Organic UV Filters from Sediment to the Ragworm Hediste diversicolor: Bioaccumulation of Benzophenone-3 and Further Proof of Octocrylene Metabolism","authors":"Fanny Clergeaud, S. Fagervold, A. Rodrigues, Evane Thorel, D. Stien, P. Lebaron","doi":"10.3390/pollutants2010004","DOIUrl":"https://doi.org/10.3390/pollutants2010004","url":null,"abstract":"Organic UV filters are continuously released in aquatic ecosystems due to their widespread use, especially in touristic coastal environments. Generally, organic UV filters are poorly soluble in water and tend to accumulate in the sediment compartment. This represents a conceivable risk for sediment-dwelling organisms and a potential for transfer of the UV filters up the food chain. This study aimed to assess the potential transfer of seven UV filters including benzophenone-3 (BP3), bis-ethylhexyloxyphenol methoxyphenyl triazine (BEMT), butyl methoxydibenzoylmethane (BM), methylene bis-benzotriazolyl tetramethylbutylphenol (MBBT), 2-ethylhexyl salicylate (ES), diethylhexyl butamido triazone (DBT), and octocrylene (OC) from artificial spiked sediment (10 µg·g−1 dry weight) to sediment-dwelling worms. All UV filters were detected in the worms after 28 days of exposure, but only BP3 was apparently bioaccumulated, with a biota sediment accumulation factor (BSAF) of 12.38 ± 4.65. However, metabolomic profiling revealed that OC was metabolized by the worms into 11 fatty acid conjugates, demonstrating that OC did also accumulate in the worms in the form of OC–fatty acid conjugates. Here, the sole quantification of the parent organic UV filter underestimated the accumulation factor and the exposure of organisms. In general, it is therefore important to pair the conventional method (BSAF calculus) with other techniques, such as metabolomics, to assess the actual potential for bioaccumulation of xenobiotics including transformed xenobiotics.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78745360","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-01-27DOI: 10.3390/pollutants2010003
Rigorous peer-reviews are the basis of high-quality academic publishing [...]
严格的同行评议是高质量学术出版的基础[…]
{"title":"Acknowledgment to Reviewers of Pollutants in 2021","authors":"","doi":"10.3390/pollutants2010003","DOIUrl":"https://doi.org/10.3390/pollutants2010003","url":null,"abstract":"Rigorous peer-reviews are the basis of high-quality academic publishing [...]","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76944435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-01-13DOI: 10.20944/preprints202201.0185.v1
D. Mendoza, T. Benney, R. Bares, B. Fasoli, Corbin Anderson, Shawn A Gonzales, E. Crosman, S. Hoch
Every day around 93% of children under the age of 15 (1.8 billion children) breathe outdoor air that is so polluted it puts their health and development at serious risk. Due to the pandemic, however, ventilation of buildings using outdoor air has become an important safety technique to prevent the spread of COVID-19. With the mounting ev-idence suggesting that air pollution is impactful to human health and educational out-comes, this contradictory guidance may be problematic in schools with higher air pol-lution levels, but keeping kids COVID-19 free and in school to receive their education is now more pressing than ever. To understand if all schools in an urban area are ex-posed to similar outdoor air quality and if school infrastructure protects children equally indoors, we installed research grade sensors to observe PM2.5 concentrations in indoor and outdoor settings to understand how unequal exposure to indoor and out-door air pollution impacts indoor air quality among high- and low-income schools in Salt Lake City, Utah. Based on this approach, we found that during atmospheric inver-sions and dust events, there was a lag ranging between 35 to 73 minutes for the out-door PM2.5 concentrations to follow a similar temporal pattern as the indoor PM2.5. This lag has policy and health implications and may help to explain the rising concerns re-garding reduced educational outcomes related to air pollution in urban areas. These data and resulting analysis show that poor air quality may impact school settings, and the potential implications with respect to environmental inequality.
{"title":"Investigation of Indoor and Outdoor Fine Particulate Matter Concentrations in Schools in Salt Lake City, Utah","authors":"D. Mendoza, T. Benney, R. Bares, B. Fasoli, Corbin Anderson, Shawn A Gonzales, E. Crosman, S. Hoch","doi":"10.20944/preprints202201.0185.v1","DOIUrl":"https://doi.org/10.20944/preprints202201.0185.v1","url":null,"abstract":"Every day around 93% of children under the age of 15 (1.8 billion children) breathe outdoor air that is so polluted it puts their health and development at serious risk. Due to the pandemic, however, ventilation of buildings using outdoor air has become an important safety technique to prevent the spread of COVID-19. With the mounting ev-idence suggesting that air pollution is impactful to human health and educational out-comes, this contradictory guidance may be problematic in schools with higher air pol-lution levels, but keeping kids COVID-19 free and in school to receive their education is now more pressing than ever. To understand if all schools in an urban area are ex-posed to similar outdoor air quality and if school infrastructure protects children equally indoors, we installed research grade sensors to observe PM2.5 concentrations in indoor and outdoor settings to understand how unequal exposure to indoor and out-door air pollution impacts indoor air quality among high- and low-income schools in Salt Lake City, Utah. Based on this approach, we found that during atmospheric inver-sions and dust events, there was a lag ranging between 35 to 73 minutes for the out-door PM2.5 concentrations to follow a similar temporal pattern as the indoor PM2.5. This lag has policy and health implications and may help to explain the rising concerns re-garding reduced educational outcomes related to air pollution in urban areas. These data and resulting analysis show that poor air quality may impact school settings, and the potential implications with respect to environmental inequality.","PeriodicalId":20301,"journal":{"name":"Pollutants","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84164536","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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