Secondary pollutant impacts from emissions of single sources may need to be assessed to satisfy a variety of regulatory requirements including the Clean Air Act New Source Review and Prevention of Significant Deterioration programs and the National Environmental Policy Act. In this work, single source impacts on O3 and secondary PM2.5 are estimated with annual 2011 photochemical grid model simulations where new hypothetical sources are added to the central and eastern United States with varying precursor emission rates and emission release heights. Impacts from these hypothetical sources are tracked with photochemical grid model source apportionment. Single source impacts on downwind 8-hr maximum O3 tend to increase as emissions of NOX or VOC increase. Downwind impacts on PM2.5 sulfate and nitrate also tend to increase as emissions of SO2 and NOX increase. For all secondary pollutants, impacts from these hypothetical sources tend to decrease as distance from the source increases. However, peak impacts on O3 and secondary PM2.5 are not at the facility fence-line but typically within 50–100 km depending on the emissions rate, precursor pollutant, and emissions release point. Downwind impacts are not uniform directionally from these sources due to varying downwind availability of chemical reactants and prevailing meteorology. Peak impacts for O3 (∼15 ppb) and PM2.5 sulfate (∼8 μg/m3) were within 50 km of these hypothetical sources and peak impacts for PM2.5 nitrate (∼1 μg/m3) were within 125 km. The daily maximum 8-hr O3 and maximum daily average PM2.5 sulfate and nitrate ion impacts for the new hypothetical sources modeled here are generally consistent with those reported in literature. Additional assessments of single source impacts on secondary pollutants are still needed to provide a more comprehensive assessment of different source types and source environments.

Passive air samplers (PAS) have become recurrent methods for environmental monitoring. However, the influence of environmental variables, such as temperature, over these devices has not been fully investigated. Since climate change is likely to induce major environmental changes, the role of the temperature needs to be studied to assure the suitability of PAS for the long-term monitoring of semi-volatile organic compounds (SVOCs) and their utility to compare data from different locations. This study aimed at evaluating the potential loss of polycyclic aromatic hydrocarbons (PAHs) in PAS containing disks of polyurethane foam (PUF) at different temperatures. The gradient of temperature inside and outside the PAS was firstly determined, being noted an internal/external difference of up to 5 °C. Secondly, a lab-controlled experiment was performed by daily analyzing PAHs in PUF-based PAS exposed to 25 °C and 38 °C, for a period of 7 days. A significant loss of PAHs in PUFs was not observed for any of both scenarios, remaining constant through time. Moreover, PAH levels were not significantly different according to the temperature. These findings indicate that the environmental temperature does not affect the stability of PAHs in PAS. Once PAHs have been uptaken, they are not easily volatilized from these devices. Consequently, PAS are good environmental monitors independently on the ambient conditions of temperature, being suitable for the comparability of data, either temporally or spatially, on the airborne concentrations of PAHs.

A reliable identification of sources and their relative time dependent contributions to ambient aerosol load is an important air pollution research problem. Given the inherent complexity of contributing sources in urban/mega-cities, an appropriate statistical investigation is needed to characterize sources and to understand their timeline trend profiles. Daily average ambient particulate matter (PM) loads, PM10 (aerodynamic diameter <10 μm) and coarser particulate matter (CPM: aerodynamic diameter >10 μm) were collected once a week over 4 years at a receptor site in Delhi. The samples were analyzed to quantify the presence of 17 marker elements. Time series data of PM loads, and that of associated marker elements was subjected to Positive Matrix Factorization (PMF) to identify sources and to quantify their contributions to each PM fraction with reference to the associated marker elements. The resolved time series data of each contributing source was further subjected to Ensemble Empirical Mode Decomposition (EEMD) analysis to extract their timeline trend profile over four years in CPM and PM10 load. Three sources contributed to the CPM load: anthropogenic (15%), primary crustal (59%), and fine crustal dust (26%). Four sources contributed to the PM10 load: coarser grain crustal material (9%), fine grain crustal material (12%), industrial and vehicular emissions (23%), and wind assisted transport and re-suspension of surface dust (56%). The timeline trend of sources contributions to CPM and PM10 displayed a non-linearity. The unique composite-PM10 source contributed maximum to the ambient PM10 load. Distinct underlying processes of this source involved convective re-suspension and city-wide cleaning associated upliftment of surface deposits back into the ambient environment.

The potential sources and ecotoxicological risks of 26 aliphatic hydrocarbons (AHs), 16 polycyclic aromatic hydrocarbons (PAHs) and total petroleum hydrocarbons (TPHs) were investigated in coastal water and sediments of Khark Island, SW Iran. The major sources of the contamination were petroleum and petroleum combustion based on the PCA analysis and diagnostic indices of AHs and PAHs, and also ring classification of PAHs. The ecological risk of both individual and multiple PAHs was quite low in sediments compared with screening benchmarks. Likewise, the low concentration of TEQ, MEQ and TEQcarc of sediments suggest low toxicity of PAHs in the study area. However, environmental control is recommended to reduce the pollution burden of PAHs in seawater. The human health risk assessment for PAHs through dermal adsorption indicated that the possibility of negative adverse effects of PAHs in sediments is rare but swimming in the vicinity of industrial facilities should be done cautiously.

The development of new dredging techniques that can reduce, or at least predict, the environmental impacts, is in high demand by governments in developing countries. In the present work, a new methodology was developed, to evaluate the level of metals contamination (i.e. cadmium, lead and zinc) of the water column, during a dredging operation. This methodology was used to evaluate the impacts of the construction of a new maritime terminal in Sepetiba Bay, Brazil. The methodology quantifies the amount of resuspended sediments and calculates the expected contaminants concentrations in the water column. The results indicated that sediment quality criteria were not compatible with water quality criteria, because the dredging of contaminated sediments does not necessarily yield contaminated water. It is suggested that the use of sediment quality criteria for dredging operations might be abandoned, and the methodology presented in this study applied to assess dredging's environmental impacts, predicting water contamination levels.

Bed sediment samples from 79 coastal New York and New Jersey, USA sites were analyzed for 75 compounds including wastewater associated contaminants, PAHs, and other organic compounds to assess the post-Hurricane Sandy distribution of organic contaminants among six regions. These results provide the first assessment of wastewater compounds, hormones, and PAHs in bed sediment for this region. Concentrations of most wastewater contaminants and PAHs were highest in the most developed region (Upper Harbor/Newark Bay, UHNB) and reflected the wastewater inputs to this area. Although the lack of pre-Hurricane Sandy data for most of these compounds make it impossible to assess the effect of the storm on wastewater contaminant concentrations, PAH concentrations in the UHNB region reflect pre-Hurricane Sandy conditions in this region. Lower hormone concentrations than predicted by the total organic carbon relation occurred in UHNB samples, suggesting that hormones are being degraded in the UHNB region.

In this study, several macrobenthic diversity investigations were performed in Yangtze Estuary Oyster Reef, the largest artificial oyster reef in China, from 2012 to 2014. The sampling sites of the south branch showed considerably higher diversity than those of the north branch. The richness measures exhibited a significant increasing trend from low- to high-salinity zone; however, the evenness measures were typically high in the middle-salinity zone. During the past decade, the results were combined with historical data to detect the changes in macrobenthos. The variation in substrate organisms and macrobenthic diversity followed a steady trend after a major fluctuation. Redundancy analysis indicated that the water salinity and substrate factors were the main indicators that influence macrobenthic distribution. All sampling sites in the south branch were protected by a nature reserve. However, the N2 and N6 sites in the north branch were subjected to severe and mild human interventions, respectively.

A study of the efficiency of hydrodynamic cavitation and separation was carried out to evaluate an innovative, environmentally safe and acceptable system for ballast water treatment for reducing the risk of introducing non-native species worldwide. Mesocosm experiments were performed to assess the morphological changes and viability of zooplankton (copepods), Artemia salina cysts, and the growth potential of marine bacteria after the hydrodynamic cavitation treatment with a different number of cycles. Our preliminary results confirmed the significant efficiency of the treatment since more than 98% of the copepods and A. salina cysts were damaged, in comparison with the initial population. The efficiency increased with the number of the hydrodynamic cavitation cycles, or in combination with a separation technique for cysts. There was also a significant decrease in bacterial abundance and growth rate, compared to the initial number and growth potential.

The dynamics of nitrogen (N) and phosphorus (P) was studied in mariculture areas around Bolinao and Anda, Philippines to examine its possible link to recurring algal blooms, hypoxia and fish kills. They occur despite regulation on number of fish farm structures in Bolinao to improve water quality after 2002, following a massive fish kill in the area. Based on spatiotemporal surveys, coastal waters remained eutrophic a decade after imposing regulation, primarily due to decomposition of uneaten and undigested feeds, and fish excretions. Relative to Redfield ratio (16), these materials are enriched in P, resulting in low N/P ratios (~6.6) of regenerated nutrients. Dissolved inorganic P (DIP) in the water reached 4μM during the dry season, likely exacerbated by increase in fish farm structures in Anda. DIP enrichment created an N-limited condition that is highly susceptible to sporadic algal blooms whenever N is supplied from freshwater during the wet season.

Concentration-synchronous-matrix-fluorescence (CSMF) spectroscopy was applied to discriminate the oil species by characterizing the concentration dependent fluorescence properties of petroleum related samples. Seven days weathering experiment of 3 crude oil samples from the Bohai Sea platforms of China was carried out under controlled laboratory conditions and showed that weathering had no significant effect on the CSMF spectra. While different feature extraction methods, such as PCA, PLS and Gabor wavelet analysis, were applied to extract discriminative patterns from CSMF spectra, classifications were made via SVM to compare their respective performance of oil species recognition. Ideal correct rates of oil species recognition of 100% for the different types of oil spill samples and 92% for the closely-related source oil samples were achieved by combining Gabor wavelet with SVM, which indicated its advantages to be developed to a rapid, cost-effective, and accurate forensic oil spill identification technique.