Acrylamide (ACR) is a toxic compound formed during high-temperature food processing and is also present in cigarette smoke. It induces oxidative stress, apoptosis, and tissue damage, including cutaneous injury. Wheat sprout (WSP), a natural antioxidant-rich agricultural product, may provide protective effects against ACR-induced skin toxicity. This study investigated the protective effects of WSP extract against ACR-induced skin damage in a rat model, with a focus on histomorphometric alterations, oxidative stress, and apoptotic regulation. Twenty adult male rats were randomly assigned to four groups (n = 5 per group): control, ACR-treated (50 mg/kg), ACR + WSP-treated (50 mg/kg ACR + 200 mg/kg WSP), and WSP-treated (200 mg/kg). The treatments were administered orally once daily for 21 days. Skin tissues were examined histologically using hematoxylin and eosin and Masson's trichrome staining. Oxidative stress biomarkers, including malondialdehyde (MDA), total antioxidant capacity (TAC), and superoxide dismutase (SOD), were measured in the serum, whereas apoptotic markers (p53 and BCL-2) were evaluated using immunohistochemistry. ACR exposure significantly reduced dermal thickness, collagen density, and hair follicle and sebaceous gland profiles, while increasing oxidative stress and apoptotic signaling. Co-administration of WSP significantly mitigated these effects by preserving skin architecture, significantly increasing TAC and SOD levels, reducing MDA concentrations, and modulating apoptotic markers. In conclusion, the WSP extract exerts a protective effect against ACR-induced skin toxicity by enhancing antioxidant defenses, inhibiting apoptosis, and preserving dermal structure, highlighting its potential as a sustainable, agriculture-derived protective agent against environmental dermatotoxicants.
{"title":"Protective effects of wheat sprouts extract against acrylamide-induced skin toxicity: Modulation of oxidative stress, apoptosis, and histomorphometric alterations in rats.","authors":"Hamid Reza Moradi, Azadeh Vafaeyan, Zabihollah Khaksar, Fatemeh Alipour","doi":"10.1007/s11356-026-37451-2","DOIUrl":"https://doi.org/10.1007/s11356-026-37451-2","url":null,"abstract":"<p><p>Acrylamide (ACR) is a toxic compound formed during high-temperature food processing and is also present in cigarette smoke. It induces oxidative stress, apoptosis, and tissue damage, including cutaneous injury. Wheat sprout (WSP), a natural antioxidant-rich agricultural product, may provide protective effects against ACR-induced skin toxicity. This study investigated the protective effects of WSP extract against ACR-induced skin damage in a rat model, with a focus on histomorphometric alterations, oxidative stress, and apoptotic regulation. Twenty adult male rats were randomly assigned to four groups (n = 5 per group): control, ACR-treated (50 mg/kg), ACR + WSP-treated (50 mg/kg ACR + 200 mg/kg WSP), and WSP-treated (200 mg/kg). The treatments were administered orally once daily for 21 days. Skin tissues were examined histologically using hematoxylin and eosin and Masson's trichrome staining. Oxidative stress biomarkers, including malondialdehyde (MDA), total antioxidant capacity (TAC), and superoxide dismutase (SOD), were measured in the serum, whereas apoptotic markers (p53 and BCL-2) were evaluated using immunohistochemistry. ACR exposure significantly reduced dermal thickness, collagen density, and hair follicle and sebaceous gland profiles, while increasing oxidative stress and apoptotic signaling. Co-administration of WSP significantly mitigated these effects by preserving skin architecture, significantly increasing TAC and SOD levels, reducing MDA concentrations, and modulating apoptotic markers. In conclusion, the WSP extract exerts a protective effect against ACR-induced skin toxicity by enhancing antioxidant defenses, inhibiting apoptosis, and preserving dermal structure, highlighting its potential as a sustainable, agriculture-derived protective agent against environmental dermatotoxicants.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146058416","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pb(II) contamination from landfill leachate poses a serious environmental and public health risk. This study demonstrates the valorisation of municipal solid waste (MSW) into an efficient Pb(II) adsorbent through MgO functionalisation of MSW-derived biochar using MgCl₂·6H₂O. Pristine biochar (P-BC) and MgO-modified biochar (MgO-BC) were synthesised from the organic fraction of MSW through pyrolysis at 450 °C. SEM and FTIR analyses confirmed enhanced porosity and the introduction of Mg-O functional groups following modification. Batch adsorption experiments showed strong pH dependence, with maximum Pb(II) removal at pH 11 of 83.50% for P-BC and 99.82% for MgO-BC. Adsorption data were best described by the Freundlich isotherm and pseudo-second-order kinetic models, indicating multilayer chemisorption on heterogeneous surfaces. Langmuir maximum adsorption capacities were 24.82 mg/g for P-BC and 36.63 mg/g for MgO-BC. Intra-particle diffusion analysis revealed that boundary layer film diffusion dominated the adsorption process. Characterisations and comparative experiments confirm that MgO functionalisation significantly improves Pb(II) adsorption performance through the synergistic effects of ion exchange, electrostatic attraction, complexation, precipitation, and pore diffusion mechanisms. Overall, the results demonstrate the potential of MSW-derived biochar as a cost-effective, sustainable solution for landfill leachate treatment, supporting circularity and resource recovery in MSW management.
{"title":"Magnesium oxide-functionalized biochar synthesis from municipal solid waste for Pb(II) removal in aqueous media and potential application in leachate remediation.","authors":"Nkululeko Sabelo Dlamini, Pawan Kumar Jha, Pradeep Kumar Sharma","doi":"10.1007/s11356-026-37461-0","DOIUrl":"https://doi.org/10.1007/s11356-026-37461-0","url":null,"abstract":"<p><p>Pb(II) contamination from landfill leachate poses a serious environmental and public health risk. This study demonstrates the valorisation of municipal solid waste (MSW) into an efficient Pb(II) adsorbent through MgO functionalisation of MSW-derived biochar using MgCl₂·6H₂O. Pristine biochar (P-BC) and MgO-modified biochar (MgO-BC) were synthesised from the organic fraction of MSW through pyrolysis at 450 °C. SEM and FTIR analyses confirmed enhanced porosity and the introduction of Mg-O functional groups following modification. Batch adsorption experiments showed strong pH dependence, with maximum Pb(II) removal at pH 11 of 83.50% for P-BC and 99.82% for MgO-BC. Adsorption data were best described by the Freundlich isotherm and pseudo-second-order kinetic models, indicating multilayer chemisorption on heterogeneous surfaces. Langmuir maximum adsorption capacities were 24.82 mg/g for P-BC and 36.63 mg/g for MgO-BC. Intra-particle diffusion analysis revealed that boundary layer film diffusion dominated the adsorption process. Characterisations and comparative experiments confirm that MgO functionalisation significantly improves Pb(II) adsorption performance through the synergistic effects of ion exchange, electrostatic attraction, complexation, precipitation, and pore diffusion mechanisms. Overall, the results demonstrate the potential of MSW-derived biochar as a cost-effective, sustainable solution for landfill leachate treatment, supporting circularity and resource recovery in MSW management.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Excessive nitrate and phosphate in water pose serious environmental and health risks, requiring effective and sustainable removal methods. This study investigates the efficiency of iron-modified biochar derived from barley straw (Fe-BSBC) for removing these pollutants from water. The influence of contact time, pH, adsorbent dosage, and competing anions on adsorption performance was tested in batch experiments. At pH 6 and 23 ± 1 °C, with an initial adsorbate concentration of 15 mg/L and adsorbent dosages of 5 g/L for phosphate and 15 g/L for nitrate, equilibrium was achieved within 8 h for phosphate and 24 h for nitrate. Fe-BSBC demonstrated adsorption capacities of 13.7 mg/g for phosphate and 2.0 mg/g for nitrate, outperforming most of the previously reported biochar adsorbents. Isotherm modelling indicated that the Sips model best described the adsorption process, suggesting multilayer and heterogeneous adsorption. Predicted maximum adsorption capacities were 22.0 mg/g for phosphate and 4.07 mg/g for nitrate. Kinetic data aligned with the pseudo-second-order model, indicating chemisorption as the primary mechanism. Electrostatic attraction was identified as the main mechanism for nitrate adsorption, evidenced by a decrease in zeta potential after nitrate uptake and supported by FTIR, EDS, and XRD characterisation. Conversely, phosphate removal was mainly driven by ligand exchange, leading to the formation of Fe-O-P complexes, alongside electrostatic interactions. Overall, Fe-BSBC presents a cost-effective and scalable water treatment solution that supports the Sustainable Development Goals.
{"title":"Iron-modified barley straw biochar for nitrate and phosphate removal from water.","authors":"Sepideh Ansari, Ricardo Bello-Mendoza, Aisling O'Sullivan","doi":"10.1007/s11356-025-37358-4","DOIUrl":"https://doi.org/10.1007/s11356-025-37358-4","url":null,"abstract":"<p><p>Excessive nitrate and phosphate in water pose serious environmental and health risks, requiring effective and sustainable removal methods. This study investigates the efficiency of iron-modified biochar derived from barley straw (Fe-BSBC) for removing these pollutants from water. The influence of contact time, pH, adsorbent dosage, and competing anions on adsorption performance was tested in batch experiments. At pH 6 and 23 ± 1 °C, with an initial adsorbate concentration of 15 mg/L and adsorbent dosages of 5 g/L for phosphate and 15 g/L for nitrate, equilibrium was achieved within 8 h for phosphate and 24 h for nitrate. Fe-BSBC demonstrated adsorption capacities of 13.7 mg/g for phosphate and 2.0 mg/g for nitrate, outperforming most of the previously reported biochar adsorbents. Isotherm modelling indicated that the Sips model best described the adsorption process, suggesting multilayer and heterogeneous adsorption. Predicted maximum adsorption capacities were 22.0 mg/g for phosphate and 4.07 mg/g for nitrate. Kinetic data aligned with the pseudo-second-order model, indicating chemisorption as the primary mechanism. Electrostatic attraction was identified as the main mechanism for nitrate adsorption, evidenced by a decrease in zeta potential after nitrate uptake and supported by FTIR, EDS, and XRD characterisation. Conversely, phosphate removal was mainly driven by ligand exchange, leading to the formation of Fe-O-P complexes, alongside electrostatic interactions. Overall, Fe-BSBC presents a cost-effective and scalable water treatment solution that supports the Sustainable Development Goals.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-26DOI: 10.1007/s11356-025-37368-2
Maria Safdar, Aqsa Mushtaq, Samiullah Akram
Carbon capture and storage (CCS) is vital for cutting CO₂ emissions and tackling climate change. The CCS innovations of the last decades can be categorized based on the post- or pre-combustion capture, oxy-fuel combustion, and chemical looping combustion (CLC) approaches used. These techniques are primarily aimed towards capturing CO2 that would be emitted from industrial sources or power plants in separate, manicured environments prior to its release into the atmosphere. For instance, post-combustion capture can be applied to coal-fired sources to extract CO₂ from flue gases, whereas pre-combustion technologies, as the name implies, remove CO₂ before fuel is burned and are typically used for gasification processes. However, despite their promise, high energy demand, large implementing costs, and long-term storage risks stay as major hurdles to mass adoption. The different levels of technology development for carbon capture and storage and carbon capture, utilization and storage (CCUS) have made significant developments for three decades, representing the continuing interests of scientists and engineers, but also have significant shortcomings in terms of efficiency, economy, and environmental impacts. This research provides evidence of the importance of CCS for reducing CO₂ emissions, a critical component in meeting global sustainability targets, especially in hard-to-decarbonize sectors. The review differs from earlier studies in that it reviews current technological innovations and assesses their performance while also recommending pathways through existing barriers to large-scale implementation.
{"title":"Strategies for mitigating carbon dioxide emissions: advanced carbon capture and storage technologies.","authors":"Maria Safdar, Aqsa Mushtaq, Samiullah Akram","doi":"10.1007/s11356-025-37368-2","DOIUrl":"https://doi.org/10.1007/s11356-025-37368-2","url":null,"abstract":"<p><p>Carbon capture and storage (CCS) is vital for cutting CO₂ emissions and tackling climate change. The CCS innovations of the last decades can be categorized based on the post- or pre-combustion capture, oxy-fuel combustion, and chemical looping combustion (CLC) approaches used. These techniques are primarily aimed towards capturing CO<sub>2</sub> that would be emitted from industrial sources or power plants in separate, manicured environments prior to its release into the atmosphere. For instance, post-combustion capture can be applied to coal-fired sources to extract CO₂ from flue gases, whereas pre-combustion technologies, as the name implies, remove CO₂ before fuel is burned and are typically used for gasification processes. However, despite their promise, high energy demand, large implementing costs, and long-term storage risks stay as major hurdles to mass adoption. The different levels of technology development for carbon capture and storage and carbon capture, utilization and storage (CCUS) have made significant developments for three decades, representing the continuing interests of scientists and engineers, but also have significant shortcomings in terms of efficiency, economy, and environmental impacts. This research provides evidence of the importance of CCS for reducing CO₂ emissions, a critical component in meeting global sustainability targets, especially in hard-to-decarbonize sectors. The review differs from earlier studies in that it reviews current technological innovations and assesses their performance while also recommending pathways through existing barriers to large-scale implementation.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146045728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-26DOI: 10.1007/s11356-026-37446-z
Nathkapach Kaewpitoon Rattanapitoon, Thawatchai Aeksanit, Jun Norkaew, Schawanya Kaewpitoon Rattanapitoon
{"title":"Comments on \"Microbial diversity and metabolic potential in long-term Cr(VI) polluted soil during in situ biostimulation: a pilot effective assay\".","authors":"Nathkapach Kaewpitoon Rattanapitoon, Thawatchai Aeksanit, Jun Norkaew, Schawanya Kaewpitoon Rattanapitoon","doi":"10.1007/s11356-026-37446-z","DOIUrl":"https://doi.org/10.1007/s11356-026-37446-z","url":null,"abstract":"","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146045746","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-26DOI: 10.1007/s11356-026-37459-8
Selva Acar, Tuğba Tuna, Nesli Ersoy
This cross-sectional study evaluated the environmental impact of athletes' dietary patterns by estimating greenhouse gas emissions (GHGE) and water footprint (WF). It also assessed knowledge, attitudes, and behaviors related to sustainable nutrition using a structured questionnaire aligned with the FAO definition of sustainable diets. Conducted between January and August 2023 in Ankara, the study included 100 elite athletes (mean age: 21.0 ± 3.3 years; 65% female) from various sports disciplines. Dietary intake was assessed using a semi-quantitative food frequency questionnaire, and GHGE and WF values were calculated based on life cycle assessment data. The mean GHGE and WF values of athletes' diets were 3017.1 ± 1877.4 g CO₂-eq/day and 5.4 ± 3.2 mL/g, respectively. Male athletes and strength/power athletes exhibited significantly higher dietary environmental impacts than female and team sports athletes (p < 0.001 and p < 0.05, respectively). Red meat and animal protein consumption were strongly associated with higher GHGE and WF values (p < 0.001). Despite the increasing importance of sustainability, more than 90% of participants lacked accurate knowledge of sustainable nutrition. Moreover, a discrepancy was observed between athletes' stated willingness to support environmental values and their actual food choices, indicating an intention-behavior gap. This study contributes to the limited literature by quantifying the environmental impact of athletes' diets while concurrently examining sustainability-related behavioral factors. The findings underscore the importance of integrating sustainability principles into sports nutrition planning and education to reduce environmental impacts while maintaining performance goals.
本横断面研究通过估算温室气体排放(GHGE)和水足迹(WF)来评估运动员饮食模式对环境的影响。它还根据粮农组织对可持续饮食的定义,使用结构化问卷评估了与可持续营养相关的知识、态度和行为。该研究于2023年1月至8月在安卡拉进行,包括来自不同体育学科的100名优秀运动员(平均年龄:21.0±3.3岁;65%为女性)。采用半定量食物频率问卷评估膳食摄入量,并根据生命周期评估数据计算GHGE和WF值。运动员膳食GHGE平均值为3017.1±1877.4 g CO₂-eq/d, WF平均值为5.4±3.2 mL/g。男性运动员和力量/力量运动员的饮食环境影响显著高于女性和团体运动运动员(p
{"title":"Environmental impact of athletes' diets: greenhouse gas emissions, water footprint, and sustainability awareness.","authors":"Selva Acar, Tuğba Tuna, Nesli Ersoy","doi":"10.1007/s11356-026-37459-8","DOIUrl":"https://doi.org/10.1007/s11356-026-37459-8","url":null,"abstract":"<p><p>This cross-sectional study evaluated the environmental impact of athletes' dietary patterns by estimating greenhouse gas emissions (GHGE) and water footprint (WF). It also assessed knowledge, attitudes, and behaviors related to sustainable nutrition using a structured questionnaire aligned with the FAO definition of sustainable diets. Conducted between January and August 2023 in Ankara, the study included 100 elite athletes (mean age: 21.0 ± 3.3 years; 65% female) from various sports disciplines. Dietary intake was assessed using a semi-quantitative food frequency questionnaire, and GHGE and WF values were calculated based on life cycle assessment data. The mean GHGE and WF values of athletes' diets were 3017.1 ± 1877.4 g CO₂-eq/day and 5.4 ± 3.2 mL/g, respectively. Male athletes and strength/power athletes exhibited significantly higher dietary environmental impacts than female and team sports athletes (p < 0.001 and p < 0.05, respectively). Red meat and animal protein consumption were strongly associated with higher GHGE and WF values (p < 0.001). Despite the increasing importance of sustainability, more than 90% of participants lacked accurate knowledge of sustainable nutrition. Moreover, a discrepancy was observed between athletes' stated willingness to support environmental values and their actual food choices, indicating an intention-behavior gap. This study contributes to the limited literature by quantifying the environmental impact of athletes' diets while concurrently examining sustainability-related behavioral factors. The findings underscore the importance of integrating sustainability principles into sports nutrition planning and education to reduce environmental impacts while maintaining performance goals.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-25DOI: 10.1007/s11356-026-37431-6
Reyes García-Garcinuño, Massimo Picardo, Josepa Fabregas, Laura Vallecillos, Francesc Borrull, Rosa Maria Marcé
An analytical method based on PM10 active sampling followed by pressurized liquid extraction and liquid chromatography-tandem mass spectrometry was developed to determine 20 per- and polyfluoroalkyl substances (PFASs). The method had good quality parameters, with method detection limits between 0.01 and 0.30 pg m-3, method quantification limits between 0.57 and 1.8 pg m-3, and recoveries above 75% for all target compounds. Analysis of air samples from two urban locations near industrial zones in Tarragona (Spain) revealed the widespread occurrence of PFASs, with perfluoro-n-butanoic acid (PFBA), perfluoro-n-pentanoic acid (PFPA), and sodium perfluoro-1-octanesulfonate (PFOS) as the most prevalent compounds at both sites. These three compounds were detected in all the samples analyzed, with the highest concentrations being 202 pg m-3 for PFBA, 178 pg m-3 for PFPA, and 109 pg m-3 for PFOS. Estimated daily intakes were calculated for infants, children, and adults under two scenarios. Risk assessment results showed individual non-carcinogenic risk values ranging from 2.4E-08 for perfluoro-n-undecanoic acid (PFUnDA) to 3.8E-01 for perfluoro-n-decanoic acid (PFDA), with the sum of all values remaining below the benchmark of 1, indicating that the risk is low. The compounds contributing most to the non-carcinogenic risk were PFDA (66.6%), PFOS (28.2%), and perfluoro-n-octanoic acid (PFOA, 5.10%). The carcinogenic risk was assessed for PFOS and PFOA, with the combined values in the range of 1.2E-06 to 3.7E-05, indicating also a low risk.
{"title":"Determination of per- and polyfluoroalkyl substances in air samples from urban areas close to industrial complexes and human risk assessment.","authors":"Reyes García-Garcinuño, Massimo Picardo, Josepa Fabregas, Laura Vallecillos, Francesc Borrull, Rosa Maria Marcé","doi":"10.1007/s11356-026-37431-6","DOIUrl":"https://doi.org/10.1007/s11356-026-37431-6","url":null,"abstract":"<p><p>An analytical method based on PM<sub>10</sub> active sampling followed by pressurized liquid extraction and liquid chromatography-tandem mass spectrometry was developed to determine 20 per- and polyfluoroalkyl substances (PFASs). The method had good quality parameters, with method detection limits between 0.01 and 0.30 pg m<sup>-3</sup>, method quantification limits between 0.57 and 1.8 pg m<sup>-3</sup>, and recoveries above 75% for all target compounds. Analysis of air samples from two urban locations near industrial zones in Tarragona (Spain) revealed the widespread occurrence of PFASs, with perfluoro-n-butanoic acid (PFBA), perfluoro-n-pentanoic acid (PFPA), and sodium perfluoro-1-octanesulfonate (PFOS) as the most prevalent compounds at both sites. These three compounds were detected in all the samples analyzed, with the highest concentrations being 202 pg m<sup>-3</sup> for PFBA, 178 pg m<sup>-3</sup> for PFPA, and 109 pg m<sup>-3</sup> for PFOS. Estimated daily intakes were calculated for infants, children, and adults under two scenarios. Risk assessment results showed individual non-carcinogenic risk values ranging from 2.4E-08 for perfluoro-n-undecanoic acid (PFUnDA) to 3.8E-01 for perfluoro-n-decanoic acid (PFDA), with the sum of all values remaining below the benchmark of 1, indicating that the risk is low. The compounds contributing most to the non-carcinogenic risk were PFDA (66.6%), PFOS (28.2%), and perfluoro-n-octanoic acid (PFOA, 5.10%). The carcinogenic risk was assessed for PFOS and PFOA, with the combined values in the range of 1.2E-06 to 3.7E-05, indicating also a low risk.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146045785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1007/s11356-026-37410-x
Swetha Madhusudanan, Radhika Venkatesan, Swapna Babu, Sellappa Nallusamy, Mithileysh Sathiyanarayanan, Marta Zurek Mortka, Jerzy Szymanski
Land being a major constrain in metro cities like Chennai has contributed to the development of closely spaced high-rise apartment complexes which lead to poor indoor air quality. Native indoor plants serve as a natural medium in absorbing air pollution entering indoors mainly through balcony spaces and also enhance the aromatic and visual quality of indoor space. This research has been carried out as a pilot study with an aim to explore the effectiveness of a planting palette comprising native flowering, air-purifying medicinal and vertical wall plants in absorbing the air pollutants in the context of an urban apartment balcony space in Chennai, Tamil Nadu, India. The level of absorption of pollutants such as carbon dioxide, carbon monoxide, total volatile organic compounds, benzene, and formaldehyde was monitored in two scenarios one planted and another non-planted balcony using Internet of Things sensors for a period of 1 month. The results observed on a Thursday for carbon dioxide, carbon monoxide, and total volatile organic compounds for non-planted balcony are 984 ppm, 392 µg/m3, and 75 µg/m3 (highest due to STP activities) when compared to planted balcony with the values 919 ppm, 335 µg/m3, and 71 µg/m3. The selected plant palette has displayed minimal absorption of formaldehyde and benzene. But both the pollutants are found to reduce gradually within 2 h in the planted balcony and 3 h in the non-planted balcony after the floor mopping activity which contributes to formaldehyde and benzene. Hence, the study proves that plants as a natural medium are inexpensive and best in absorbing air pollutants thereby improving the quality of the indoor environment.
{"title":"Enhancing the indoor air quality in an urban apartment as in the case of Chennai using native plants.","authors":"Swetha Madhusudanan, Radhika Venkatesan, Swapna Babu, Sellappa Nallusamy, Mithileysh Sathiyanarayanan, Marta Zurek Mortka, Jerzy Szymanski","doi":"10.1007/s11356-026-37410-x","DOIUrl":"https://doi.org/10.1007/s11356-026-37410-x","url":null,"abstract":"<p><p>Land being a major constrain in metro cities like Chennai has contributed to the development of closely spaced high-rise apartment complexes which lead to poor indoor air quality. Native indoor plants serve as a natural medium in absorbing air pollution entering indoors mainly through balcony spaces and also enhance the aromatic and visual quality of indoor space. This research has been carried out as a pilot study with an aim to explore the effectiveness of a planting palette comprising native flowering, air-purifying medicinal and vertical wall plants in absorbing the air pollutants in the context of an urban apartment balcony space in Chennai, Tamil Nadu, India. The level of absorption of pollutants such as carbon dioxide, carbon monoxide, total volatile organic compounds, benzene, and formaldehyde was monitored in two scenarios one planted and another non-planted balcony using Internet of Things sensors for a period of 1 month. The results observed on a Thursday for carbon dioxide, carbon monoxide, and total volatile organic compounds for non-planted balcony are 984 ppm, 392 µg/m<sup>3</sup>, and 75 µg/m<sup>3</sup> (highest due to STP activities) when compared to planted balcony with the values 919 ppm, 335 µg/m<sup>3</sup>, and 71 µg/m<sup>3</sup>. The selected plant palette has displayed minimal absorption of formaldehyde and benzene. But both the pollutants are found to reduce gradually within 2 h in the planted balcony and 3 h in the non-planted balcony after the floor mopping activity which contributes to formaldehyde and benzene. Hence, the study proves that plants as a natural medium are inexpensive and best in absorbing air pollutants thereby improving the quality of the indoor environment.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146043598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1007/s11356-026-37444-1
Lena Herwanger, Katharina Sternecker, Jan Kühnisch, Franz-Xaver Reichl, Christof Högg
Bisphenol A (BPA) is an endocrine-disrupting compound widely used in plastics and resins and associated with metabolic, reproductive, and neurodevelopmental disorders. Infants and toddlers are particularly vulnerable because detoxification capacity is immature and exposure occurs during sensitive developmental stages. While BPA is banned in infant feeding bottles within the European Union, its use in pacifiers remains unregulated despite frequent "BPA-free" labeling. This study quantified BPA migration from seven commercially available pacifiers and assessed potential exposure relative to the newly revised European Food Safety Authority (EFSA) tolerable daily intake (TDI; 0.2 ng kg⁻1 bw day⁻1) in a worst-case exposure scenario. Pacifiers were dissected into shield and teat components, cut into fragments, and analyzed separately using validated high-performance liquid chromatography with fluorescence detection (HPLC-FLD). Measured BPA concentrations in the eluates (c(BPA,HPLC)) ranged from below the limit of quantification (LOQ) up to 288 µg/L. Based on these measured values, the extrapolated total BPA release per pacifier was 33 to 26,536 ng, with the highest migration observed in a "BPA-free" labeled product. Even the lowest total migration exceeded the 2023 EFSA TDI, whereas exposures would have been negligible under the former 2015 t-TDI (4 µg kg⁻1 bw day⁻1). These findings demonstrate that pacifiers can constitute a relevant early-life source of BPA exposure and contribute to already critical background levels. The results underline the unreliability of voluntary "BPA-free" claims and emphasize the need for harmonized EU regulation analogous to existing restrictions for feeding bottles and toys.
双酚A (BPA)是一种内分泌干扰化合物,广泛用于塑料和树脂中,与代谢、生殖和神经发育障碍有关。婴幼儿尤其容易受到影响,因为他们的排毒能力还不成熟,而且暴露在敏感的发育阶段。尽管欧盟禁止在婴儿奶瓶中使用双酚a,但在安抚奶嘴中的使用仍不受监管,尽管经常贴上“不含双酚a”的标签。这项研究量化了7种市售奶嘴的BPA迁移量,并评估了在最坏的情况下,相对于欧洲食品安全局(EFSA)新修订的每日可耐受摄入量(TDI; 0.2 ng kg - 1 bw - 1)的潜在暴露量。将奶嘴拆分为护罩和奶嘴两部分,切成碎片,分别使用高效液相色谱-荧光检测(HPLC-FLD)进行分析。洗脱液中测定的BPA浓度(c(BPA,HPLC))范围从低于定量限(LOQ)到288µg/L。根据这些测量值,推断出每个奶嘴的总BPA释放量为33至26,536 ng,在标有“不含BPA”的产品中观察到的迁移量最高。即使是最低的总迁移量也超过了2023年欧洲食品安全局的TDI,而根据2015年的TDI(4µkg kg bw d毒血症),暴露量可以忽略不计。这些发现表明,安抚奶嘴可能是早期BPA暴露的相关来源,并导致已经达到临界背景水平。研究结果强调了自愿声明“不含双酚a”的不可靠性,并强调了欧盟需要制定协调一致的法规,类似于目前对奶瓶和玩具的限制。
{"title":"Migration of bisphenol A from commercially available pacifiers: HPLC-FLD analysis and exposure assessment in infants and toddlers.","authors":"Lena Herwanger, Katharina Sternecker, Jan Kühnisch, Franz-Xaver Reichl, Christof Högg","doi":"10.1007/s11356-026-37444-1","DOIUrl":"https://doi.org/10.1007/s11356-026-37444-1","url":null,"abstract":"<p><p>Bisphenol A (BPA) is an endocrine-disrupting compound widely used in plastics and resins and associated with metabolic, reproductive, and neurodevelopmental disorders. Infants and toddlers are particularly vulnerable because detoxification capacity is immature and exposure occurs during sensitive developmental stages. While BPA is banned in infant feeding bottles within the European Union, its use in pacifiers remains unregulated despite frequent \"BPA-free\" labeling. This study quantified BPA migration from seven commercially available pacifiers and assessed potential exposure relative to the newly revised European Food Safety Authority (EFSA) tolerable daily intake (TDI; 0.2 ng kg⁻<sup>1</sup> bw day⁻<sup>1</sup>) in a worst-case exposure scenario. Pacifiers were dissected into shield and teat components, cut into fragments, and analyzed separately using validated high-performance liquid chromatography with fluorescence detection (HPLC-FLD). Measured BPA concentrations in the eluates (c(BPA,HPLC)) ranged from below the limit of quantification (LOQ) up to 288 µg/L. Based on these measured values, the extrapolated total BPA release per pacifier was 33 to 26,536 ng, with the highest migration observed in a \"BPA-free\" labeled product. Even the lowest total migration exceeded the 2023 EFSA TDI, whereas exposures would have been negligible under the former 2015 t-TDI (4 µg kg⁻<sup>1</sup> bw day⁻<sup>1</sup>). These findings demonstrate that pacifiers can constitute a relevant early-life source of BPA exposure and contribute to already critical background levels. The results underline the unreliability of voluntary \"BPA-free\" claims and emphasize the need for harmonized EU regulation analogous to existing restrictions for feeding bottles and toys.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146040006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1007/s11356-026-37412-9
Francesca Ferretti, Andrea Barbarossa, Anisa Bardhi
Per- and polyfluoroalkyl substances (PFAS) are a group of synthetic chemicals characterized by a fluorinated carbon chain that confers unique physicochemical properties. Widely used in industrial and consumer products, including textiles, food packaging, and firefighting foams, PFAS are highly persistent in the environment, earning them the designation of "forever chemicals." Their stability contributes to their widespread diffusion across different environmental compartments (water, soil, air) and multiple exposure pathways (e.g., diet). These lead to PFAS bioaccumulation and biomagnification, which poses a substantial threat to both ecosystems and human health. Exposure to PFAS has been associated with a range of adverse health effects, including liver damage, thyroid disease, immunotoxicity, reproductive issues, and various cancers in both humans and animals. While regulatory efforts have led to the phase-out of long-chain PFAS such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), emerging research suggest that their short-chain replacements may also raise health concerns. This review applies a One Health framework to explore the interconnected impacts of these contaminants on human, animal, and environmental health. Furthermore, it highlights knowledge gaps that hinder comprehensive risk assessment and management, emphasizing the need for a globally coordinated, multidisciplinary approach to address the multifaceted challenges posed by PFAS.
{"title":"An overview of the impact of PFAS on animals, humans, and the environment using a One Health approach.","authors":"Francesca Ferretti, Andrea Barbarossa, Anisa Bardhi","doi":"10.1007/s11356-026-37412-9","DOIUrl":"https://doi.org/10.1007/s11356-026-37412-9","url":null,"abstract":"<p><p>Per- and polyfluoroalkyl substances (PFAS) are a group of synthetic chemicals characterized by a fluorinated carbon chain that confers unique physicochemical properties. Widely used in industrial and consumer products, including textiles, food packaging, and firefighting foams, PFAS are highly persistent in the environment, earning them the designation of \"forever chemicals.\" Their stability contributes to their widespread diffusion across different environmental compartments (water, soil, air) and multiple exposure pathways (e.g., diet). These lead to PFAS bioaccumulation and biomagnification, which poses a substantial threat to both ecosystems and human health. Exposure to PFAS has been associated with a range of adverse health effects, including liver damage, thyroid disease, immunotoxicity, reproductive issues, and various cancers in both humans and animals. While regulatory efforts have led to the phase-out of long-chain PFAS such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), emerging research suggest that their short-chain replacements may also raise health concerns. This review applies a One Health framework to explore the interconnected impacts of these contaminants on human, animal, and environmental health. Furthermore, it highlights knowledge gaps that hinder comprehensive risk assessment and management, emphasizing the need for a globally coordinated, multidisciplinary approach to address the multifaceted challenges posed by PFAS.</p>","PeriodicalId":545,"journal":{"name":"Environmental Science and Pollution Research","volume":" ","pages":""},"PeriodicalIF":5.8,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146040003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}