Neurobiomarker and body temperature responses to recreational marathon running.

OBJECTIVES: To assess how biomarkers indicating central nervous system insult (neurobiomarkers) vary in peripheral blood with exertional-heat stress from prolonged endurance exercise. DESIGN: Observational study of changes in neuron specific enolase (NSE), S100 calcium-binding protein B (S100ß), Glial Fibrillary Acid Protein (GFAP) and Ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCHL1) at Brighton Marathon 2022. METHODS: In 38 marathoners with in-race core temperature (Tc) monitoring, exposure (High, Intermediate or Low) was classified by cumulative hyperthermia - calculated as area under curve of Time × Tc > 38 °C - and also by running duration (finishing time). Blood was sampled for neurobiomarkers, cortisol and fluid-regulatory stress surrogates, including copeptin and creatinine (at rested baseline; within 30 min of finishing; and at 24 h). RESULTS: Finishing in 236 ±â€¯40 min, runners showed stable GFAP and UCH-L1 across the marathon and next-day. Significant (P < 0.05) increases from baseline were shown post-marathon and at 24 h for S100ß (8.52 [3.65, 22.95] vs 39.0 [26.48, 52.33] vs 80.3 [49.1, 99.7] ng·L-1) and post-marathon only for NSE (3.73 [3.30, 4.32] vs 4.85 [4.45, 5.80] µg·L-1, P < 0.0001). Whilst differential response to hyperthermia was observed for cortisol, copeptin and creatinine, neurobiomarker responses did not vary. Post-marathon, only NSE differed by exercise duration (High vs Low, 5.81 ±â€¯1.77 vs. 4.69 ±â€¯0.73 µg·L-1, adjusted P = 0.0358). CONCLUSIONS: Successful marathon performance did not associate with evidence for substantial neuronal insult. To account for variation in neurobiomarkers with prolonged endurance exercise, factors additional to hyperthermia, such as exercise duration and intensity, should be further investigated.

A direct method to quantify methanol-soluble organic carbon for brown carbon absorption studies.

The current research provides a newly developed method to quantify methanol-soluble organic carbon (MeS_OC) in aerosol samples. This analytical procedure allows an accurate separation of MeS-OC component, which is critical for the calculation of mass absorption efficiency (MAE) of ambient Brown Carbon (BrC) and consequently its climate relevant potential. The method includes extraction, filtering and condensation stages, leading to the preparation of a highly concentrated product in which MeS-OC can be precisely quantified by a Sunset Carbon Analyzer in a single analysis step. This method can be applied on aerosol collected using either high or low volume samplers, since a relatively small filter area is required for the determination. Furthermore, it eliminates any misestimation of the MeS-OC mass that may appear in other reported techniques that don't seem to include the precise separation of methanol-soluble fraction in their quantification process.•The mass quantification of methanol-soluble organic carbon is essential, contributing up to 50% to the absorptivity of organic aerosol (BrC) at shorter wavelengths.•The method provides a direct measurement of methanol-soluble aerosol components, resolving any potential uncertainties of previously applied methods.•The adoption of this direct quantification approach leads to a rationalization of past MAE estimates for BrC with implications for radiative transfer models.

Brown carbon absorption and radiative effects under intense residential wood burning conditions in Southeastern Europe: New insights into the abundance and absorptivity of methanol-soluble organic aerosols.

Biomass burning is a major source of Brown Carbon (BrC), strongly contributing to radiative forcing. In urban areas of the climate-sensitive Southeastern European region, where strong emissions from residential wood burning (RWB) are reported, radiative impacts of carbonaceous aerosols remain largely unknown. This study examines the absorption properties of water- and methanol-soluble organic carbon (WSOC, MeS_OC) in a city (Ioannina, Greece) heavily impacted by RWB. Measurements were performed during winter (December 2019 - February 2020) and summer (July - August 2019) periods, characterized by RWB and photochemical processing of organic aerosol (OA), respectively. PM2.5 filter extracts were analyzed spectrophotometrically for water- and methanol-soluble BrC (WS_BrC, MeS_BrC) absorption. WSOC concentrations were quantified using TOC analysis, while those of MeS_OC were determined using a newly developed direct quantification protocol, applied for the first time to an extended series of ambient samples. The direct method led to a mean MeS_OC/OC of 0.68 and a more accurate subsequent estimation of absorption efficiencies. The mean winter WS_BrC and MeS_BrC absorptions at 365 nm were 13.9 Mm-1 and 21.9 Mm-1, respectively, suggesting an important fraction of water-insoluble OA. Mean winter WS_BrC and MeS_BrC absorptions were over 10 times those observed in summer. MeS_OC was more absorptive than WSOC in winter (mean mass absorption efficiencies - MAE365: 1.81 vs 1.15 m2 gC-1) and especially in summer (MAE: 1.12 vs 0.27 m2 gC-1) due to photo-dissociation and volatilization of BrC chromophores. The winter radiative forcing (RF) of WS_BrC and MeS_BrC relative to elemental carbon (EC) was estimated at 8.7 % and 16.7 %, respectively, in the 300-2500 nm band. However, those values increased to 48.5 % and 60.2 % at 300-400 nm, indicating that, under intense RWB, BrC forcing becomes comparable to that of soot. The results highlight the consideration of urban BrC emissions in radiative transfer models, as a considerable climate forcing factor.

Apportionment of black and brown carbon spectral absorption sources in the urban environment of Athens, Greece, during winter.

This study examines the spectral properties and source characteristics of absorbing aerosols (BC: Black Carbon; BrC: Brown Carbon, based on aethalometer measurements) in the urban background of Athens during December 2016-February 2017. Using common assumptions regarding the spectral dependence of absorption due to BC (AAEBC = 1) and biomass burning (AAEbb = 2), and calculating an optimal AAEff value for the dataset (1.18), the total spectral absorption was decomposed into five components, corresponding to absorption of BC and BrC from fossil-fuel (ff) combustion and biomass burning (bb), and to secondary BrC estimated using the BC-tracer minimum R-squared (MRS) method. Substantial differences in the contribution of various components to the total absorption were found between day and night, due to differences in emissions and meteorological dynamics, while BrC and biomass burning aerosols presented higher contributions at shorter wavelengths. At 370 nm, the absorption due to BCff contributed 36.3% on average, exhibiting a higher fraction (58.1%) during daytime, while the mean BCbb absorption was estimated at 18.4%. The mean absorption contributions due to BrCff, BrCbb and BrCsec were 6.7%, 32.3% and 4.9%, respectively. The AbsBCff,370 component maximized during the morning traffic hours and was strongly correlated with NOx (R2 = 0.76) and CO (R2 = 0.77), while a similar behavior was seen for the AbsBrCff,370 component. AbsBCbb and AbsBrCbb levels escalated during nighttime and were highly associated with nss-K+ and with the organic aerosol (OA) components related to fresh and fast-oxidized biomass burning (BBOA and SV-OOA) as obtained from ACSM measurements. Multiple linear regression was used to attribute BrC absorption to five OA components and to determine their absorption contributions and efficiencies, revealing maximum contributions of BBOA (33%) and SV-OOA (21%). Sensitivity analysis was performed in view of the methodological uncertainties and supported the reliability of the results, which can have important implications for radiative transfer models.

Human health risk assessment for toxic elements in the extreme ambient dust conditions observed in Sistan, Iran.

This study evaluates the bioaccessibility and health risks related to heavy metals (Cd, Cr, Co, Cu, Mn, Ni, Pb, Zn and metalloid As) in airborne dust samples (TSP and PM2.5) in Zabol, Iran during the summer dust period, when peak concentration levels of PM are typically observed. High bioaccessibilities of carcinogenic metals in PM2.5 (i.e. 53.3%, 48.6% and 47.6% for Ni, Cr and As, respectively) were calculated. The carcinogenic and non-carcinogenic health risks were assessed for three exposure pathways (inhalation, ingestion and dermal contact), separately for children and adults. Non-carcinogenic inhalation risks were very high (Hazard Index: HI > 1) both for children and adults, while the carcinogenic risks were above the upper acceptable threshold of 10-4 for adults and marginally close (5.0-8.4 × 10-5) for children. High carcinogenic risks (>10-4) were found for the ingestion pathway both for children and adults, while HI values > 1 (8.2) were estimated for children. Carcinogenic and non-carcinogenic risk estimates for dermal contact were also above the limits considered acceptable, except for the carcinogenic risk for children (7.6 × 10-5). Higher non-carcinogenic and carcinogenic risks (integrated for all elements) were associated with the inhalation pathway in adults and children with the exception of carcinogenic risk for children, where the ingestion route remains the most important, while As was linked with the highest risks for nearly all exposure pathways. A comparative evaluation shows that health risks related with toxic elements in airborne particles in Sistan are among the highest reported in the world.

Long-term brown carbon spectral characteristics in a Mediterranean city (Athens).

This study analyses 4-years of continuous 7-λ Aethalometer (AE-33) measurements in an urban-background environment of Athens, to resolve the spectral absorption coefficients (babs) for black carbon (BC) and brown carbon (BrC). An important BrC contribution (23.7 ± 11.6%) to the total babs at 370 nm is estimated for the period May 2015-April 2019, characterized by a remarkable seasonality with winter maximum (33.5 ± 13.6%) and summer minimum (18.5 ± 8.1%), while at longer wavelengths the BrC contribution is significantly reduced (6.8 ± 3.6% at 660 nm). The wavelength dependence of the total babs gives an annual-mean AAE370-880 of 1.31, with higher values in winter night-time. The BrC absorption and its contribution to babs presents a large increase reaching up to 39.1 ± 13.6% during winter nights (370 nm), suggesting residential wood burning (RWB) emissions as a dominant source for BrC. This is supported by strong correlations of the BrC absorption with OC, EC, the fragment ion m/z 60 derived from ACSM and PMF-analyzed organic fractions related to biomass burning (e.g. BBOA). In contrast, BrC absorption decreases significantly during daytime as well as in the warm period, reaching to a minimum during the early-afternoon hours in all seasons due to photo-chemical degradation. Estimated secondary BrC absorption is practically evident only during winter night-time, implying the fast oxidation of BrC species from RWB emissions. Changes in mixing-layer height do not significantly affect the BrC absorption in winter, while they play a major role in summer.

Elemental and organic carbon in the urban environment of Athens. Seasonal and diurnal variations and estimates of secondary organic carbon.

Elemental and organic carbon (EC and OC) hourly concentrations were measured continuously, at an urban location in central Athens, Greece, for an 8-month period (January-August). Average concentrations of 2.2 µgC m(-3) and 6.8 µgC m(-3) were observed, for EC and OC, respectively. The combined contribution of carbonaceous compounds (EC plus organic matter) to PM(10) was calculated at 26%. The seasonal variability of EC was limited, while OC mean concentrations were significantly higher (by 23%), during the warm months (May-August). The weekly variation followed a different pattern, with the weekend decrease of EC levels (25%) being more pronounced than of OC (14%). EC produced a bimodal diurnal cycle, with the morning rush hour traffic mode prevailing. The OC mean circadian variation displayed those peaks as well. However, midday-to-afternoon presence of secondary organic aerosol (SOA) was strongly indicated. The conditional probability function was used to assess the impact of wind direction. High EC, OC levels were linked to southern flows, which during summer are mainly related to the appearance of sea breeze circulation. The temporal variation of EC, OC and their correlation patterns with primary and secondary gaseous pollutants, suggested that, although primary emissions affected both fractions, SOA formation is an important factor to be accounted for, especially during the photochemical season. Secondary organic carbon was estimated using the EC tracer method and orthogonal regression on OC, EC hourly concentration data. The average contributions of secondary organic carbon (SOC) to OC were calculated at 20.9% for the cold period and 30.3% for the warm period. Maximum values of 58% and 91% were estimated for daily and hourly contributions, respectively. The SOC diurnal variations suggested photochemical formation throughout the year, intensified during summer months, with the correlation coefficient between SOC and the sum of oxidants (NO(2+)O(3)) reaching up to 0.84.

An overview of the PM10 pollution problem, in the Metropolitan Area of Athens, Greece. Assessment of controlling factors and potential impact of long range transport.

The present study analyzes PM(10) concentration data collected by the Greek air quality monitoring network at 8 sites over the Greater Athens Area, for the period of 2001-2004. The primary objectives were to assess the degree of compliance with the EU-legislated air quality standard for PM(10) and also provide an overall statistical examination of the factors controlling the seasonal and spatial variation of concentrations, over the wider urban agglomeration. Daily concentrations, averaged over the whole study period, ranged between 32.3 and 60.9 microg m(-3). The four-year average concentration of PM(10) at five sites exceeded the annual limit value of 40 microg m(-3), while most of the sites surpassed the allowed percentage of exceedances of the daily limit value (50 microg m(-3)), for each of the four years. The seasonal variation of PM(10) levels was not found to be uniform across the eight sites, with average cold-period concentrations being higher at four of them and warm period concentrations being significantly higher at three sites, which also displayed recurring annual variation of monthly concentrations. Concentration levels displayed moderate spatial heterogeneity. Nevertheless significant inter-site correlations were observed (ranging between 0.55 and 085). The determination of the spatial correlation levels relied mainly on site types rather than on inter-site distances. Monitoring sites were classified accordingly using cluster analysis in two groups presenting distinct spatiotemporal variation and affected by different particle formation processes. The group including urban sites was mainly affected by primary, combustion-related processes and especially vehicular traffic, as it was also deduced through the examination of the diurnal distribution of particulate levels and through factor analysis. On the contrary, suburban background sites seemed more affected by particle transport from more polluted neighboring areas and secondary particle formation through gaseous precursors, both processes aided from favoring meteorological conditions. The association of the PM(10) levels with backwards trajectories was also examined, in an attempt to account for the possible long range transport of particles in Athens. It was found that a notable part of area-wide episodic events could be attributed to trans-boundary transport of particles, with the origins of some severe dust outbreaks traced back to the Sahara desert and the Western Mediterranean.

Toxic metal content of particulate matter (PM10), within the Greater Area of Athens.

This study presents results from a yearlong particulate matter measurement campaign, conducted across the Greater Athens Area, at four locations, between 1st June 2001 and 31st May 2002. The collected PM(10) 24-h samples were analyzed for nine toxic metals and metalloids (Pb, As, Cd, Ni, Cr, Mn, V, Cu, Hg). Concerning the five elements regulated by the European Union, annual average concentrations of Pb were found below the limit values at all sites, Cd and Ni concentrations were lower than the prospective assessment thresholds at all sites, concentrations of As exceeded the assessment threshold at two sites, while concentrations of Hg were found below detection limits in all samples. Concentration levels of Mn and V were in compliance with the values proposed by the World Health Organization. The seasonal and spatial variability of metal concentrations was examined and site-specific correlation analysis was conducted for the identification of metals with similar origin. The association between trace metals and NO(x) concentrations was explored to account for the impact of automotive sources, at two traffic-impacted sites. Cu was the metal most closely linked with the road transport sector. The relation of concentration levels with the prevalence of winds from different sectors was studied in an effort to investigate the transport of metal particles from various zones of the city. Finally, factor analysis was carried out to extract the main components responsible for the variance of the dataset and to attribute them to specific source categories, with vehicle-related sources being important in all cases.

Particulate matter and black smoke concentration levels in central Athens, Greece.

This study presents the statistical analysis of PM(10) and PM(2.5) concentrations (measured at a central site, in the Athens area), along with black smoke (BS) data, for a 2-year period. The biennial average concentrations of PM(10) and PM(2.5) were 75 and 40 microg m(-3). The respective average concentration of BS, as estimated by the OECD method, was 108 microg m(-3). Severe exceedances of the PM(10) air quality standards were recorded. The seasonal variation of PM(10) and BS was less pronounced than the variation of PM(2.5), which concentration was elevated by 14.2% during the cold period. Concentrations of all three pollutants were significantly lower during weekends; however, PM(2.5) and BS displayed a more uniform weekly distribution pattern. PM(10) particles were found to be almost equally comprised by PM(2.5) and PM(10-2.5) particles (PM(2.5)/PM(10) ratio=0.53+/-0.09 microg/m(3)). The average PM(10)/BS value was found lower than unity revealing the inappropriateness of the used reflectance conversion method, for the estimation of mass-equivalent BS concentrations, in the study area, where diesel-powered vehicles mainly control emissions of light-absorbing substances. Important reductions in concentrations were observed during days when drivers of diesel-powered taxies and transportation buses went on strike (reaching 40% for BS). Calm wind conditions were found to have an incremental effect on particle concentrations and were also associated with the appearance of persistent episodic events. Increased PM levels were also observed during southern-southwestern wind flows while significantly lower-than-average concentrations were measured during precipitation events. Separate regression analyses were performed for PM(10), PM(2.5) with BS and NO(x) as independent variables, in an attempt to estimate the relative contribution of specific source types (diesel-powered vehicles) to measured particle levels. The contribution of the diesel-exhaust component to PM(10) mass was estimated at 49.9%, while the corresponding contributions to PM(2.5) mass concentrations was 53.8%. These results may have important implications with the oncoming decision of national authorities to allow the purchase of diesel-powered private cars to the residents of the Greater Athens Area, which was forbidden up to this day.