Shifting seasons greatly influence the use and management practices in residential built environments which subsequently affect the level of exposure to various pollutants indoors. The levels of fine particulate matter (PM2.5) were monitored in fifteen households of Lahore, Pakistan during different seasons. DustTrak aerosol monitors (model 8520, TSI Inc.) were run simultaneously in the kitchens and living rooms of the selected sites for seventy two hours each. To aid analysis, houses were categorized in three groups according to floor area. For non–smoking houses there was little variation between 24h average PM2.5 concentrations in kitchens (270 to 295μg/m3) although there was an increase in concentrations in living rooms as floor area increased. Across all houses the average PM2.5 concentration was observed to vary during the seasons. In the kitchens the average PM levels were 326μg/m3 during the spring falling to 133μg/m3 in summer, 180μg/m3 in monsoon, 395μg/m3 in autumn and 448μg/m3 during the winter. Similarly, in the living rooms, the mean PM levels observed were 190μg/m3 in spring, 101μg/m3 in summer, 158μg/m3 in monsoon, 458μg/m3 in autumn and 590μg/m3 in winter. Factors contributing towards these levels were cooking (involving frequent frying), floor sweeping, and also movement of the occupants. Smoking at two sites and use of gas heaters during the winter were also identified as contributing sources. Apart from these sources, ventilation was identified to be the most singular attributing factor to the above mentioned variations in PM levels. Ventilation during the warm season ranged from 3.51 air changes per hour (ACH) to 7.68 ACH. On the contrary, ventilation decreased during the autumn and winter season (2.5 to 5.64 ACH) and this resulted in an accumulation of PM indoors. The levels of fine particulate matter were observed to be 3 to 23 times higher than the WHO established standard of 25μg/m3.

Freshwater cyanobacteria produce highly toxic substances such as microcystins (MCs), and water containing MCs is often discharged to downstream and coastal areas. We conducted field monitoring in Isahaya Bay to clarify the short-term dynamics of MCs discharged from a reservoir following a cyanobacteria bloom in the warm season. MCs were detected in the seawater of the bay (max. 0.10μgL−1), and were deposited on the sea floor, with the MC content of the surface sediment increasing by approximately five times (0.11±0.077–0.53±0.15μgkgww−1, mean±SD) at the four stations near the reservoir drainage gate before and after the discharge. The MCs was then transported from the mouth of the bay by tidal currents during the period of the study. Therefore, the MCs were moved away from the closed water area where the cyanobacteria blooms, and spread throughout the coastal area.

The recurrent emergence of infections outbreaks associated with shellfish consumption is an important health problem, which results in substantial economic losses to the seafood industry. Even after depuration, shellfish is still involved in outbreaks caused by pathogenic bacteria, which increases the demand for new efficient strategies to control the shellfish infection transmission. Phage therapy during the shellfish depuration is a promising approach, but its success depends on a detailed understanding of the dynamics of bacterial communities in the harvesting waters. This study intends to evaluate the seasonal dynamics of the overall bacterial communities, disease-causing bacterial populations and bacterial sanitary quality indicators in two authorized harvesting-zones at Ria de Aveiro.During the hot season, the total bacterial community presented high complexity and new prevalent populations of the main shellfish pathogenic bacteria emerged. These results indicate that the spring/summer season is a critical period during which phage therapy should be applied.

The drinking water treatment plant (WTP) of the city of Turin (NW Italy), with a treatment capacity of 40 × 10⁶ m³/year, has a basin that is employed as a lagooning pretreatment facility. This study aims to assess the effect of the basin on several environmental parameters (temperature, dissolved oxygen (DO), turbidity, pH, chloride, nitrite, and total chlorophyll) of the river water before entering the WTP and monitor the changes inside the basin caused by the seasonal hydrological and biological cycles. Sampling was carried out on 16 dates over 3 years at the inlet and outlet channel of the basin and in five locations along three depth values (1, 6, and 12 m, i.e., at the bottom). The results of the 3-year monitoring campaign demonstrated that the basin had an effect on pH (p = 6.6 × 10⁻⁹), DO (p = 0.000072), turbidity (p = 0.011), and chlorophyll (p = 0.033). No significant changes regarding nitrite (p = 0.11), chloride (p = 0.94), and temperature (p = 0.66) were detected. The results gathered from the sampling campaign inside the basin demonstrated that, during the year, the basin experienced the following: two states of complete mixing in early spring and fall, when the differences in temperature between the surface and the bottom of the basin were less than 1 °C; a condition of late spring/summer stratification with a temperature difference between the surface and the bottom of 4–5 °C and a difference in DO, pH, and total chlorophyll concentration that increased throughout the spring season; and one or more states of summer circulation due to the weak stability of the warm season stratification. During the states of circulation, the persistent algae photosynthetic activity tended to cause a quick change in the concentration of DO, total chlorophyll, and pH value in the most superficial layer of the basin. The results of the principal component analysis (PCA) showed a strong direct relationship between the weight of the first component and the hydrodynamic states of the basin (stratification/circulation) and an inverse relationship between the weight of the second component and the intensity of photosynthetic activity of algae species.

With the generalized linear model and natural splines (ns), we examined the association between outdoor air pollutants and daily morbidity for diabetes and liver disease stratified by sexes and ages based on 4 years of daily data (2008–2011) in Tianjin, China. Season effects of air pollutants including particulate matter (PM), sulfur dioxide (SO₂), and nitrogen dioxide (NO₂) were also investigated. An increase of 10 μg/m³in a 2-day average concentrations of particulate matter with diameters of 10 μm or less (PM₁₀), SO₂, and NO₂corresponds to increases in diabetes morbidity of 0.39 % (95 % confidence interval (CI), −0.42–1.12), 0.15 % (95 % CI, −0.25–0.54), and 1.22 % (95 % CI, 0.51–2.96), respectively. As for liver morbidity, the increases were −0.84 % (95 % CI, −2.33–0.62), 0.90 % (95 % CI, 0.50–1.74), and 1.10 % (95 % CI, −2.58–4.78), respectively. The effects were stronger in the cool season than those in the warm season; females and the elderly were generally more vulnerable to outdoor air pollution. This study possesses scientific implications and instructional significance for local environmental standards and medical policymaking.

An investigation of atmospheric mercury was conducted in the urban coastal zone of the Gulf of Gdansk (Baltic Sea, Poland) in 2008. Rainwater samples were collected in bulk samplers and Hg concentration was determined using AAS method. Total mercury concentration ranged from 1.9 to 14.8 ng l⁻¹(the mean was 8.3 ng l⁻¹with standard deviation ±3.7), out of which about 34 % were water-soluble Hg(II) forms. Distribution of Hg species in rainwater was related to both the emission source and the atmospheric processes. During the sampling period, two maxima of Hg concentration in precipitation were observed: the first in the cold season and the second one in the warm season. Elevated concentrations of Hg in wintertime precipitation were generally the result of local urban atmospheric emission connected with the following anthropogenic sources: intensive combustion of fossil fuels in domestic furnaces, individual power/heat generating plants, and motor vehicles. During summertime, Hg° re-emitted from contaminated land and sea surfaces was photochemically oxidized by active atmospheric substances (e.g., hydroxyl radicals, hydrogen peroxide, halogens) and could be an additional source of atmospherically deposited Hg. The results presented in this work indicate that rainwater Hg concentration and deposition values are not much higher in comparison with other urban locations along the Baltic Sea basin and other coastal cities. However, the elevated mercury concentration in rainwater and, consequently, higher deposition ratio could appear occasionally as an effect of intensive anthropogenic emissions (domestic heating) and/or photochemical reactions.

Epidemiological studies have widely demonstrated association between ambient ozone and mortality, though controversy remains, and most of them only use a certain metric to assess ozone levels. However, in China, few studies have investigated the acute effects of ambient ozone, and rare studies have compared health effects of multiple daily metrics of ozone. The present analysis aimed to explore variability of estimated health effects by using multiple temporal ozone metrics. Six metrics of ozone, 1-h maximum, maximum 8-h average, 24-h average, daytime average, nighttime average, and commute average, were used in a time-series study to investigate acute mortality associated with ambient ozone pollution in Guangzhou, China, using 3 years of daily data (2006–2008). We used generalized linear models with Poisson regression incorporating natural spline functions to analyze the mortality, ozone, and covariate data. We also examined the association by season. Daily 1- and 8-h maximum, 24-h average, and daytime average concentrations yielded statistically significant associations with mortality. An interquartile range (IQR) of O₃ metric increase of each ozone metric (lag 2) corresponds to 2.92 % (95 % confidence interval (CI) 0.24 to 5.66), 3.60 % (95 % CI, 0.92 to 8.49), 3.03 % (95 % CI, 0.57 to 15.8), and 3.31 % (95 % CI, 0.69 to 10.4) increase in daily non-accidental mortality, respectively. Nighttime and commute metrics were weakly associated with increased mortality rate. The associations between ozone and mortality appeared to be more evident during cool season than in the warm season. Results were robust to adjustment for co-pollutants, weather, and time trend. In conclusion, these results indicated that ozone, as a widespread pollutant, adversely affects mortality in Guangzhou.

Spatial and temporal variability of carbon species in rainwater (bulk deposition) was studied for the first time at two sites located in urban area of Poznań City and protected woodland area (Jeziory), in central Poland, between April and December 2013. The mean concentration of total carbon (TC) for the first site was 5.86 mg L⁻¹, whereas for the second, 5.21 mg L⁻¹. Dissolved organic carbon (DOC) concentration accounted for, on average, 87 and 91 % of total carbon in precipitation at urban and non-urban sites, respectively. Significant changes in TC concentrations in rainwater were observed at both sites, indicating that atmospheric transformation, transport, and removal mechanisms of carbonaceous particles were affected by seasonal fluctuations in biogenic/anthropogenic emission and meteorological conditions (i.e., precipitation height and type, atmospheric transport). During the warm season, the DOC concentration in rainwater was mostly influenced by mixed natural and anthropogenic sources. In contrast, during the cold season, the DOC concentration significantly increased mainly as a result of anthropogenic activities, i.e., intensive coal combustion, domestic wood burning, high-temperature processes, etc. In addition, during the winter measurements, significant differences in mean DOC concentration (Kruskal-Wallis test, p < 0.05) were determined for rain, mixed rain-snow, and snow samples. It was found that rainwater TOC concentration measured in Poznań and Jeziory reflected a combination of local, regional, and distant sources. Backward trajectory analysis showed that air masses advected from polluted regions in western Europe largely affect the DOC amount in rainwater, both at urban and non-urban sites. These data imply that carbonaceous compounds are of crucial importance in atmospheric chemistry and should be considered as an important parameter while considering wet deposition, reactions with different substances, especially over polluted environments.