Combustion Of Organic Matter Research Articles

Slow post-fire carbon balance recovery despite increased net uptake rates in Alaskan tundra

Abstract Increasing wildfire occurrence and intensity have immediate effects on northern ecosystems due to combustion of aboveground vegetation and belowground soil organic matter. These immediate impacts have indirect and longer term effects, including deepening of the active layer, changes in soil decomposition rates, and shifts in plant community composition. Despite the increasing fire impacts across the tundra region, the implications of wildfire on ecosystem carbon balance are not well understood. Using paired eddy covariance towers in unburned and burned tundra, we examined the effects of a 2015 wildfire on carbon dioxide and methane fluxes in a wetland tundra ecosystem in the Yukon–Kuskokwim Delta, Alaska, from 2020 to 2022. Wildfire increased the amplitude and variability of carbon uptake and release on seasonal and annual timescales and increased the temperature sensitivity of soil respiration. Seven years post fire, there was annual net uptake in both unburned and burned tundra based on net ecosystem exchange, with the sink strength of burned tundra exceeding that of the unburned tundra by 1.18–1.64 times. However, when considering emissions, it would take approximately 86 years to recover the carbon lost from the wildfire itself. Soil moisture was a dominant driver of fluxes and positively associated with higher rates of carbon dioxide uptake and release and methane release. This study underscores the importance of understanding the effects of wildfire-induced shifts on tundra carbon cycling, allowing better predictions of long-term landscape-scale climate feedbacks as the climate continues to warm.

Effects of Fire on Physical and Chemical Properties of Soil in Fwangnin Bokkos District, Nigeria

Background: Vegetation burning, a common agricultural practice, has both positive and negative effects on soil fertility. Soil quality, which is critical for ecosystems, shapes biodiversity and productivity, while increased temperatures from vegetation burning can alter conditions for seed germination by reducing nutrient availability. Objectives: The study aims to assess the impacts of vegetation burning on soil fertility in Fwangnin, Bokkos, Nigeria, through experimental investigation of the effects of burning on both the chemical and physical properties of soil. The results are expected to contribute to the development of adaptive fire management strategies in land use, and the results will also help monitor soil changes in order to maintain long-term soil fertility. Methods: Using purposive sampling, four 500-gram soil samples were taken from 0 – 15 cm depth in burned and unburned areas. The samples were analysed for pH, electrical conductivity (EC), organic carbon (OC), organic matter (OM), nitrogen (N), phosphorus (P), and cation exchange capacity (CEC). Traditional well-proven methods were used for the analysis. Results: It was found that the pH of the burnt soil samples ranged from 6.10 to 5.90, while that of the unburnt samples ranged from 5.73 to 5.81; a significant increase in pH occurs at higher combustion temperatures, which increases the alkalinity of the soil due to the alkaline properties of ash. The electrical conductivity value for the samples in the burnt areas was significantly higher (0.08 mS/cm and 0.10 mS/cm) compared to the healthy soil (0.07 mS/cm and 0.09 mS/cm), which can be explained by the release of mineral ions due to the combustion of organic matter. The study found a decrease in organic carbon content in the burnt soil, a significant deficiency of nitrogen and a decrease in the cation exchange capacity, which contributes to the depletion of the fertile layer and a decrease in the ability of the soil to retain essential nutrients. Increased levels of organic phosphorus were also found in burnt soils, which contributes to improved crop growth and increased yields in the short term. Conclusion: The current study has filled the gap in deep understanding of the impact of vegetation burning on the fertile properties of agricultural soils. Namely, it has been experimentally established and confirmed by the results of similar studies and statistical analysis that while vegetation burning remains a common agricultural practice in Fwangnin, the long-term implications for soil fertility, structure, and ecosystem health are significant. The soil degradation observed in this study suggests that continued reliance on burning as a land-clearing method may undermine agricultural productivity and environmental integrity over time.

Satellite derived air pollution climatology over India and its neighboring regions: Spatio-temporal trends and insights

This study examines the spatial and temporal variations of key air pollutants, including Nitrogen Dioxide (NO₂), Carbon Monoxide (CO), Tropospheric Ozone (O₃), Sulfur Dioxide (SO₂), Aerosol Optical Depth (AOD), and Formaldehyde (HCHO) over India and neighboring regions, using satellite data from 2005 to 2022. Peak NO₂ (∼11–13 × 101⁵molecules/cm2) occurs in pre-monsoon and winter, mainly over urban centers, thermal plants, and crop-burning areas, emphasizing anthropogenic emissions. High CO levels (2.0–2.3 × 101⁸molecules/cm2) during summer dominate in Indo-Gangetic Plains (IGP), Eastern India, and Northeastern region, linked to the incomplete combustion of organic matter (e.g., natural forest fires and biofuel-based household cooking). Stable CO trends reflect effective government policies promoting cleaner fuels. Tropospheric O₃ shows a spatial gradient, with higher values in northern and coastal regions influenced by sunlight, humidity, and precursor emissions. Seasonal peaks in summer are governed by solar intensity, while the December peak over the northern region is likely due to dynamical transport from O₃-rich areas. SO₂ hotspots in IGP, central and eastern India, especially during winter (∼1.3–1.9 × 101⁵molecules/cm2), are attributed to local anthropogenic emissions and fossil fuel combustion such as coal. Long-term trends reveal rising SO₂ levels. AOD hotspots occur over IGP, Central and Southern India, with particularly high values during the pre-monsoon (0.5–0.6) and winter seasons. HCHO shows hotspots in the IGP, west coast, eastern, and northeastern regions, peaking in summer (7.5–8.5 × 101⁵molecules/cm2) due to biogenic VOC emissions. This study underscores the need for integrated policies to mitigate emissions, improve air quality, and protect public health.

Nanomaterial-mediated strategies for enhancing bioremediation of polycyclic aromatic hydrocarbons: A systematic review

Polycyclic aromatic hydrocarbons (PAHs) are pervasive organic pollutants in the environment that are formed as an outcome of partial combustion of organic matter. PAHs pose a significant threat to ecological systems and human health due to their cytotoxic and genotoxic effects. Therefore, an immediate need for effective PAH remediation methods is crucial. Although nanomaterials are effective for remediation of PAHs, concerns regarding environmental compatibility and sustainability remains. Therefore, this study emphasizes integration of nanomaterials with bioremediation methods, which might offer a more sustainable and ecofriendly approach to PAHs remediation. A systematic search was conducted through scholarly databases from 2013 to 2023. A total of 360 articles were scrutinized, among which 26 articles were selected that resonated with the application of nano-bioremediation. These literatures comprise both comparative analysis of bioremediation only as well as nano-bioremediation. There is an elevation of 18.9 % in PAHs removal of liquid-phase samples, when comparing bioremediation (52.2 %) with nano-bioremediation (71.1 %). A consistent trend was observed in soil samples, with bioremediation and nano-bioremediation that successfully remove PAHs, with 60.8 % and 75.1 % respectively, indicating a 14.3 % improvement. Furthermore, the review elaborated on the various features of nanomaterials that led to their efficiency in the bioremediation of PAH. The review also discussed the strategies of nano-bioremediation namely nanomaterial-assisted microbial degradation, nanomaterial-assisted enzyme-enhanced microbial activity, nanomaterial-immobilized microbial cells, nanomaterial-facilitated electron transfer, and even some eco-green approaches to remediate PAHs, like biogenic nanomaterial for PAHs.

Effects of fire and fire-induced changes in soil properties on post-burn soil respiration

Abstract Background Boreal forests cover vast areas of land in the northern hemisphere and store large amounts of carbon (C) both aboveground and belowground. Wildfires, which are a primary ecosystem disturbance of boreal forests, affect soil C via combustion and transformation of organic matter during the fire itself and via changes in plant growth and microbial activity post-fire. Wildfire regimes in many areas of the boreal forests of North America are shifting towards more frequent and severe fires driven by changing climate. As wildfire regimes shift and the effects of fire on belowground microbial community composition are becoming clearer, there is a need to link fire-induced changes in soil properties to changes in microbial functions, such as respiration, in order to better predict the impact of future fires on C cycling. Results We used laboratory burns to simulate boreal crown fires on both organic-rich and sandy soil cores collected from Wood Buffalo National Park, Alberta, Canada, to measure the effects of burning on soil properties including pH, total C, and total nitrogen (N). We used 70-day soil incubations and two-pool exponential decay models to characterize the impacts of burning and its resulting changes in soil properties on soil respiration. Laboratory burns successfully captured a range of soil temperatures that were realistic for natural wildfire events. We found that burning increased pH and caused small decreases in C:N in organic soil. Overall, respiration per gram total (post-burn) C in burned soil cores was 16% lower than in corresponding unburned control cores, indicating that soil C lost during a burn may be partially offset by burn-induced decreases in respiration rates. Simultaneously, burning altered how remaining C cycled, causing an increase in the proportion of C represented in the modeled slow-cycling vs. fast-cycling C pool as well as an increase in fast-cycling C decomposition rates. Conclusions Together, our findings imply that C storage in boreal forests following wildfires will be driven by the combination of C losses during the fire itself as well as fire-induced changes to the soil C pool that modulate post-fire respiration rates. Moving forward, we will pair these results with soil microbial community data to understand how fire-induced changes in microbial community composition may influence respiration.

SOURCE APPORTIONMENT OF ATMOSPHERIC AND SEDIMENTARY PAHS FROM KOLKATA, INDIA USING COMPOUND-CLASS-SPECIFIC RADIOCARBON ANALYSIS (CCSRA)

ABSTRACT Polycyclic aromatic hydrocarbons (PAHs) are major air pollutants that are ubiquitously produced by the combustion of organic materials, and it is extremely important to identify their pollution sources. In this study, molecular fingerprinting and compound class-specific radiocarbon dating (CCSRA) were performed on PAHs from canal sediments and air samples collected in Kolkata, India’s third largest city (population approximately 16 million), where PAHs pollution has been a serious problem. Average PAH (Σ12-parent PAHs) concentrations in air samples were 65.1 ng m–3 in summer and 70.9 ng m–3 in winter and in canal sediments were 32.7 µg g–1, which are classified as “very high-level” pollution. Molecular fingerprinting using methyl-PAH/PAH (MPAHs/PAHs) ratios and isomer pair ratios with molecular weights of 178, 202, 228, and 276 suggested that wood and coal combustion were the dominant sources of PAHs in the sediment, and that atmospheric PAHs were influenced by oil combustion in addition to them. The fraction of contemporary carbon (ƒC) of sedimentary PAHs (0.056–0.100), together with the extremely low MPAHs/PAHs ratio results, lead to the conclusion that the major source of the high concentration of PAHs in the canals is from coal combustion. On the other hand, the ƒC of atmospheric PAHs (0.272–0.369) was close to the share of biomass fuels in India’s domestic fuel consumption in 2011 (about 35%). Furthermore, the observed ƒC-discrepancy between atmospheric and sedimentary PAHs in the same urban environment was interpreted to give an insight into the loading pathway of PAHs to canal sediments in Kolkata.

Exploring naphthalene vapor biofiltration: performance and microbial community dynamics with diverse inoculums

AbstractBackgroundNaphthalene is a polycyclic aromatic hydrocarbon, highly dangerous for human health. It is produced as a byproduct of incomplete combustion of organic material and is frequently present in the air. Biofilters offer an effective alternative for its treatment. The aim of this work was to study the treatment of naphthalene vapors through biofiltration using two biofilters: one inoculated with a consortium composed of Fusarium solani and Rhodococcus erythropolis (BF1), and the other inoculated with a consortium of microbial isolates obtained from a previous biofilter eliminating naphthalene vapors.ResultsThe results demonstrate that inoculating a biofilter with a reconstructed consortium of microbial isolates from a naphthalene vapor‐eliminating biofilter allowed a reduction of the startup time from 35 to 5 days, while maintaining a consistent removal capacity (6 g m−3 h−1, equivalent to 80% removal efficiency). It was also observed that the biofilter inoculated with the reconstructed consortium exhibited comparable robustness to a biofilter previously operated for 4 months with naphthalene, with a maximum removal capacity of 14 g m−3 h−1 for a naphthalene inlet load of 17 g m−3 h−1. The study of microbial communities indicates an increase in the bacterial variability, while fungal variability remains low, with Fusarium solani being predominant at 97%.ConclusionsResults obtained during the startup of both biofilters and by challenging biofilters to increasing naphthalene concentrations or decreasing empty bed residence time showed that startup time can be reduced sevenfold by selecting the microbial consortium. An equivalent performance, in the long run, was achieved for both biofilters. © 2024 Society of Chemical Industry (SCI).

A vortex-assisted MSPD method for the extraction of Polycyclic Aromatic Hydrocarbons from shrimp with determination by GC-MS/MS

Polycyclic Aromatic Hydrocarbons (PAHs) are organic compounds with two or more condensed aromatic rings, formed from incomplete organic matter combustion. PAHs pose potential health risks due to their carcinogenic and mutagenic properties, accumulating in edible tissues of aquatic organisms, such as shrimp, which is extensively produced in the southern region of Rio Grande do Sul state (Brazil) and it is the most consumed seafood globally. Therefore, this study aimed to optimize and validate an analytical method for extracting 16 priority PAHs from shrimp samples using Vortex-Assisted Matrix Solid-Phase Dispersion (VA-MSPD) with determination by Gas Chromatography Tandem Mass Spectrometry (GC-MS/MS). The optimized method, which uses a reused solid support, was validated according to INMETRO and SANTE guidelines. PAHs demonstrated adequate linearity with correlation coefficients > 0.99. The matrix effect was assessed, and 12 out of the 16 PAHs showed a matrix effect of less than ±20%. The method's quantification limits ranged from 6.67 to 33.35 ng g-1. Accuracy and precision showed recovery values ranging from 55 to 115% with relative standard deviation (RSD) lower than 17% for all PAHs. In the applicability, 11 PAHs were detected, such as benzo[a]pyrene and benzo[b]fluoranthene, and the ∑PAHs ranged from 25.14 to 79.52 ng g-1, confirming the environmental contamination in the region and the need for monitoring these contaminants in shrimp destined for human consumption.

Synergistic Toxicity of Pollutant and Ultraviolet Exposure from a Mitochondrial Perspective.

Ultraviolet (UV) exposure and atmospheric pollution are both independently implicated in skin diseases such as cancer and premature aging. UVA wavelengths, which penetrate in the deep layers of the skin dermis, exert their toxicity mainly through chromophore photosensitization reactions. Benzo[a]pyrene (BaP), the most abundant polycyclic aromatic hydrocarbon originating from the incomplete combustion of organic matter, could act as a chromophore and absorb UVA. We and other groups have previously shown that BaP and UVA synergize their toxicity in skin cells, which leads to important oxidation. Even if mitochondria alterations have been related to premature skin aging and other skin disorders, no studies have focused on the synergy between UV exposure and pollution on mitochondria. Our study aims to investigate the combined effect of UVA and BaP specifically on mitochondria in order to assess the effect on mitochondrial membranes and the consequences on mitochondrial activity. We show that BaP has a strong affinity for mitochondria and that this affinity leads to an important induction of lipid peroxidation and membrane disruption when exposed to UVA. Co-exposure to UVA and BaP synergizes their toxicity to negatively impact mitochondrial membrane potential, mitochondrial metabolism and the mitochondrial network. Altogether, our results highlight the implication of mitochondria in the synergistic toxicity of pollution and UV exposure and the potential of this toxicity on skin integrity.

SIMULATION THE PROCESSES OF ORGANIC MATERIALS DESTRUCTION AND COMBUSTION PROCESSES CONDITION OF FIRE INTENSEICATION

Problem statement. The rapid occurrence and development of fires are caused by the occurrence of combustible materials and structures in their focus. This complicates, and in some cases makes impossible, effective firefighting, evacuation, and rescue of people and property. In order to correctly assess fire resistance, effectively increase fire resistance, and change the flammability of materials, it is necessary to study the materials burning process. The purpose of the article. To study of the combustion of easily dispersible substances and the development of gaseous reactions and their combination using the example of wood combustion. Methods. We use mathematical modeling of combustion and destructive processes under the high temperatures, taking into account the rules of thermodynamics. Research results. The conducted analysis showed that the selection of the main stages in the simulation of wood combustion is much less developed than in the case of the combustion of gas systems. It is especially difficult to do this to describe the combustion of wood, on the surface of which there is an interaction of masses (and heat) during the combustion of individual components, and the size of the front surface per unit cross-section of the sample may also change over time. Therefore, the definition of the main stage in wood burning should be used mainly in the qualitative analysis of the process, and quantitative models of wood burning should be built, if possible, taking into account all the determining factors characterizing the phenomena. Scientific novelty. For the first time, on the basis of the modeling of organic material combustion is proposed. We determine the patterns of destructive processes, which, depending on the temperature, have common patterns of qualitative and quantitative characteristics. The chemical phasing and its connection with the physical phasing of the transformation of combustible organic materials dispersed in the surface layer with the overall thermal effect of the combustion wave were determined. Practical value. The identification of stages during the wave burning of wood allows for a qualitative display of processes depending on the spatial zone and its distance from the gas zone, which allows predicting the development of protective means of organic materials against combustion.

Polycyclic aromatic compounds in a northern freshwater ecosystem: Patterns, sources, and the influences of environmental factors

Polycyclic aromatic compounds (PACs) - a large group of organic chemicals naturally present in petroleum deposits (i.e., petrogenic) or released into the environment by incomplete combustion of organic materials (i.e., pyrogenic) - represent a potential risk to the health of aquatic ecosystems. In high latitude freshwater ecosystems, concentrations of PACs may be increasing, yet there are limited studies in such systems to assess change and to understand threats. Using 10 years of contemporary data from passive samplers deployed across five regions (n = 43 sites) in the Mackenzie River Basin, we (i) describe baseline levels of PACs, (ii) assess spatiotemporal patterns, and (iii) evaluate the extent to which environmental factors (fire, snowmelt, and proximity to oil infrastructure) influence concentrations in this system. Measured concentrations were low, relative to those in more southern systems, with mixtures primarily being dominated by non-alkylated, low molecular weight compounds. Concentrations were spatially consistent, except for two sites near Norman Wells (an area of active oil extraction) with increased levels. Similarly, observed annual variation was minimal, with 2014 having generally higher levels of PACs. We did not detect effects of fire, snowmelt, or oil infrastructure on concentrations. Taken together, our findings suggest that PACs in the Mackenzie River are currently at low levels and are primarily petrogenic in origin. They further indicate that ongoing monitoring and testing of environmental drivers (especially at finer spatial scales) are needed to better predict how ecosystem change will influence PAC levels in the basin and in other northern systems.

Clustered Carbon Monoxide Poisoning Cases: Accidental Poisoning In A Vehicle

Carbon monoxide (CO) is a product of combustion of organic matter in the presence of inadequate supply of oxygen. Common sources are burning fuel, engine exhaust, burning of animal dung, heater emissions and gas geyser. It is a toxic, clear, colorless and tasteless gas. The clinical presentation runs a spectrum, ranging from headache and dizziness to coma and death. Here we report three cases that presented to us in the month of November 2023 with history, sign & symptoms suggestive of CO poisoning. Bangladesh Crit Care J March 2024; 12 (1): 72-74

Assessment of PAH exposure and health risks among South Korean firefighters based on urinary PAH metabolites

Polycyclic aromatic hydrocarbons (PAHs) comprise a group of compounds resulting from the incomplete combustion of organic matter. Firefighters engaged in fire suppression are highly exposed to PAHs. This study centered on evaluating the exposure levels and health risks of PAHs in South Korean firefighters involved in firefighting activities. The concentrations of 10 PAH metabolites in the urine of firefighters were measured immediately after, and two weeks post their engagement in extinguishing a large tire factory fire. The levels of OH-PAHs in urine samples immediately after fire suppression were elevated by a factor of 1.01–1.84 compared to urine samples from non-exposed period. The median concentration of total PAH metabolites (OH-PAHs) was higher in urine samples immediately after fire suppression (5910 ng/g creatinine) than in urine samples from non-exposed periods (5020 ng/g creatinine). However, the ∑OH-PAH levels in firefighters’ urine were related to personal habits such as smoking. The concentrations of all individual OH-PAHs in the urine samples of nonsmokers exhibited a substantial increase, ranging from 1.37 to 2.3 times, clearly demonstrating that firefighting activities were a substantial source of PAH exposure. The calculated values associated with the health risks stemming from exposure to PAHs, including carcinogenic risk, total estimated daily intake (TEDI), and hazard quotients/index (HQs/HI), all fell within acceptable limits, indicating negligible risk. However, the HQ/HI values and TEDI for individual and total PAH exposures, except those for naphthalene, were 1.36–2.00 times higher in firefighters' samples taken after firefighting operations compared to those during regular duty. This underscores the need for more comprehensive investigations to comprehend the singular impact of firefighting activities due to the diverse sources of PAH emissions in the environment.

Lipid Peroxidation as the Mechanism Underlying Polycyclic Aromatic Hydrocarbons and Sunlight Synergistic Toxicity in Dermal Fibroblasts.

Light and atmospheric pollution are both independently implicated in cancer induction and premature aging. Evidence has been growing more recently on the toxic synergy between light and pollutants. Polycyclic aromatic hydrocarbons (PAHs) originate from the incomplete combustion of organic matter. Some PAHs, such as the Benzo[a]pyrene (BaP), absorb ultraviolet A (UVA) wavelengths and can act as exogenous chromophores, leading to synergistic toxicity through DNA damage and cytotoxicity concomitant to ROS formation. In this study, we shed light on the mechanism underlying the toxic synergy between PAHs and UVA. Using dermal fibroblasts co-exposed to UVA and BaP, we have demonstrated that the photosensitization reaction causes mortality, which is most likely caused by ROS accumulation. We have shown that these ROS are concentrated in the lipids, which causes an important induction of lipid peroxidation and malondialdehyde, by-products of lipid peroxidation. We have also shown the accumulation of bulky DNA damage, most likely generated by these by-products of lipid peroxidation. To our knowledge, this study represents the first one depicting the molecular effects of photo-pollution on dermal skin.

Hepatoprotective Effects of Flavonoids against Benzo[a]Pyrene-Induced Oxidative Liver Damage along Its Metabolic Pathways.

Benzo[a]pyrene (B[a]P), a highly carcinogenic polycyclic aromatic hydrocarbon primarily formed during incomplete organic matter combustion, undergoes a series of hepatic metabolic reactions once absorbed into the body. B[a]P contributes to liver damage, ranging from molecular DNA damage to the onset and progression of various diseases, including cancer. Specifically, B[a]P induces oxidative stress via reactive oxygen species generation within cells. Consequently, more research has focused on exploring the underlying mechanisms of B[a]P-induced oxidative stress and potential strategies to counter its hepatic toxicity. Flavonoids, natural compounds abundant in plants and renowned for their antioxidant properties, possess the ability to neutralize the adverse effects of free radicals effectively. Although extensive research has investigated the antioxidant effects of flavonoids, limited research has delved into their potential in regulating B[a]P metabolism to alleviate oxidative stress. This review aims to consolidate current knowledge on B[a]P-induced liver oxidative stress and examines the role of flavonoids in mitigating its toxicity.

Benzo[a]pyrene exposure affects colorectal cancer susceptibility by regulating ERβ-mediated LINC02977 transcription

Environmental pollutants known as polycyclic aromatic hydrocarbons (PAHs) are produced through the incomplete combustion of organic material. While PAHs have been investigated as genotoxicants, they can also operate through nongenotoxic pathways in estrogen-dependent malignancies, such as breast, cervical and ovarian cancer. However, whether PAHs induce colorectal cancer (CRC) risk through estrogenic effects is still illusive. Here, we systematically investigated the abnormal expression and activation of estrogen receptor beta (ERβ) regulated by PAHs in CRC as well as the underlying mechanisms of ERβ-mediated CRC risk. Based on the 300 plasma samples from CRC patients and healthy controls detected by GC–MS/MS, we found that the plasma concentrations of benzo[a]pyrene (BaP) were significantly higher in CRC cases than in healthy controls, with significant estrogenic effects. Moreover, histone deacetylase 2 (HDAC2)-induced deacetylation of the promoter decreases ERβ expression, which is associated with poor overall survival and advanced tumor stage. The study also revealed that BaP and estradiol (E2) had different carcinogenic effects, with BaP promoting cell proliferation and inhibiting apoptosis, while E2 had the opposite effects. Additionally, this study mapped ERβ genomic binding regions by performing ChIP-seq and ATAC-seq and identified genetic variants of rs1411680 and its high linkage disequilibrium SNP rs6477937, which were significantly associated with CRC risk through meta-analysis of two independent Chinese population genome-wide association studies comprising 2,248 cases and 3,173 controls and then validation in a large-scale European population. By integrating data from functional genomics, we validated the regulatory effect of rs6477937 as an ERβ binding-disrupting SNP that mediated allele-specific expression of LINC02977 in a long-range chromosomal interaction manner, which was found to be highly expressed in CRC tissues. Overall, this study suggests that the different active effects on ERβ by PAHs and endogenous E2 may play a crucial role in the development and progression of CRC and highlights the potential of targeting ERβ and its downstream targets for CRC prevention and treatment.

Artificial formation of benzene polycarboxylic acids during sample processing of black carbon analysis: the role of organic carbon amount

Black carbon is also known as pyrogenic carbon formed by partial combustion of organic material under limited oxygen supply. It occurs along a continuum from original organic slightly charred material to highly aromatic combustion residues such as charcoal, graphite, and soot. Black carbon is extensively studied in various environments due to its ubiquity. It is also important for the biochar community because it can specifically trace the stable polycondensed part of biochar. Different methods have been adopted for black carbon determination; among them using benzene polycarboxylic acids (BPCA) as molecular markers for the polycondensed aromatic moieties of charred materials. However, different researchers have shown interferences from organic matter during BPCA analysis. Therefore, the aim of this work was to assess if artificial formation of BPCA occurs in soil samples when the organic carbon load exceeds 5–10 mg. For this purpose, we conducted black carbon analysis of different soil samples with varying TOC contents of up to 20 mg. In addition, organic matter-rich plant materials were used as a black carbon-free control (leaves of Ivy and Beech, leaves/needles of Spruce and needles of Thuja). To exclude the high-pressure digestion as source of artificial black carbon formation, a comparison between the conventional and a microwave-assisted extraction (MAE) oxidation process was included. Our results show that for soil samples, no artificial BPCA formation occurred at least up to 20 mg of total organic carbon. Higher sample weights are unrealistic for BPCA analysis of soils using current methodology. Therefore, our results clearly demonstrate that there is no artificial BPCA formation during properly performed black carbon analysis of soil samples. On the contrary, for some samples, BPCA contents tended to decrease with increasing sample weight, and thus increasing amount of TOC. In contrast, for plant samples, artificial BPCA formation of up to 3 g kg−1 occurred when more plant material equivalent to 10 mg total organic carbon was used. However, there was no amount dependence of artificial BPCA formation. The reason for artificial BPCA formation was not the high-pressure digestion, as microwave-assisted digestion showed comparable results. However, for real-world analysis, this artificial BPCA formation is not relevant because such high soil sample weights cannot be used. Nevertheless, when using organic-rich material such as peat and charred materials, the samples should contain less than 10 mg of total organic carbon.Graphical

Impacts of Forest Fires on Soil: Exploring the Effects on Biotic and Abiotic Components

Forest fires are a widespread occurrence in ecosystems worldwide, impacting both vegetation and soil. The effects of forest fires, as well as prescribed fires, on forest soil are complex, influencing soil organic matter, macro and micro-nutrients, and physical properties such as texture, color, pH, and bulk density, along with soil biota. The magnitude of the impact on forest soil depends on factors such as fire intensity, fuel load, and soil moisture. The severity and frequency of fire determine whether it is beneficial or harmful to the soil. Low-intensity fires can enhance plant available nutrients through the combustion of litter and soil organic matter, promoting rapid growth of herbaceous plants and increased nutrient storage. Conversely, high intensity fires can lead to complete loss of soil organic matter, volatilization of vital elements (N, P, S, K), and microbial death. Additionally, intense forest fires generate hydrophobic organic compounds that result in water-repellent soils. Forest fires also have long-term effects on forest soil. This paper aims to review the impacts of forest fires on various soil properties crucial for maintaining a healthy ecosystem.

Understanding Polycyclic Aromatic Hydrocarbons (PAHs) and Derivatives: Sources, Properties, and Health Impacts

PAHs, persistent organic pollutants (POPs), composed of 2-7 fused aromatic rings, emerge from processes involving incomplete combustion of organic materials. Released into the ambient air as vapors or adsorbed onto airborne particulate matter, these compounds undergo complex photochemical reactions with atmospheric pollutants such as ozone, NOX, SOX, and OH radicals and result in the formation of its derivatives which possess remarkably higher toxicity and carcinogenicity than its parent PAHs. This chapter delves into the contemporary knowledge surrounding Polycyclic Aromatic Hydrocarbons (PAHs) and their derivatives, shedding light on their sources, formation mechanisms, and inherent properties. It also comprehensively reviews the global status.

Fluorimetric determination of aqueous formaldehyde employing heating and ultrasound-assisted approach through its derivatization with a ß-diketone-nickel(2+) complex immobilized in a PMMA flow cell

Formaldehyde (FA) is a highly toxic substance present in many matrices, including freshwater as well as found in natural mechanisms such as rainfall and combustion of organic matter. Consumption of water contaminated with high levels of FA can cause severe short-term or long-term health problems. Due to these health risks, procedures are necessary to determine and quantify FA in aqua sources This paper reports on a study of fluorimetric determination of FA using a nickel(2 + )-diketonate coordination compound immobilized as a solid precursor. The compound was characterized by electronic absorption, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), thermogravimetry (TG), optical microscopy (OM), and scanner electron microscopy (SEM). The methodology was based on the reaction of the synthesized compound with an ammoniacal buffer generating a selective reagent for formaldehyde: fluoral-P. The product of the reaction generates 3,5-diacetyl-1,4-dihydrolutidine (DDL), which is responsible for the fluorescence of the system. Several parameters such as temperature, duration of heating time, and dilution effect with the best effects were studied to carry out FA determination. Under the optimum experimental conditions, a linear response ranging from 1.0 to 10.0 mg/L FA (R = 0.997 and n = 10), and a detection (3σ criterion) and quantification (10 σ criterion) limit estimated at 0.129 and 0.389 mg/L, respectively were achieved. The FA analysis was able to be conducted in 05 min with a relative standard deviation estimated at 1.10 %.