Losses of deuterated polycyclic aromatic hydrocarbons (PAHs) used as performance reference compounds (PRCs) in semipermeable membrane devices deployed at fifteen coastal sampling sites near Harstad harbour in Northern Norway were used to investigate photodegradation of these photosensitive compounds. Unusual PRC dissipation profiles, especially for samplers exposed <5m below the water surface are indicative of photodegradation. A strong correlation between loss rates for d12-chrysene and d12-benzo[e]pyrene with consistently higher losses of the latter was found. The observed photodegradation rates may be sufficiently high to impact PAH masses absorbed by a factor of two. This study demonstrates that photodegradation during exposure of passive water samplers needs to be taken into account, particularly with deployments close to the water surface, when using SPMD canisters, or when sampling in the Arctic.

The concentrations of organic carbon (OC), elemental carbon (EC), water soluble inorganic ionic components (WSIC), and major & trace elements of PM10 were studied in Delhi, an urban site of the Indo Gangetic Plain (IGP), India during January 2013 to June 2014. The average mass concentration of PM10 recorded as 249.7 ± 103.9 μg m−3 (average ± standard deviation) with a range of 61.4–584.8 μg m−3. The strong seasonal variation was noticed in the mass concentration of PM10 and its chemical composition with maxima during winter (PM10: 293.9 ± 95.6 μg m−3; OC: 30.5 ± 13.7 μg m−3; EC: 15.2 ± 7.4 μg m−3) and minima during monsoon (PM10: 143.9 ± 36.3 μg m−3; OC: 19.9 ± 16.2 μg m−3; EC: 7.4 ± 5.4 μg m−3). The average concentration of major and trace elements (Na, Mg, Al, P, S, Cl, K, Ca, Si, Cr, Ti, As, Br, Pb, Fe, Zn and Mn) was accounted for ∼18.5% of PM10 mass. Results of Positive Matrix Factorization (PMF) model, HYSPLIT4 trajectory model, PSCF analysis and cluster analysis provide region of sources and its strength and types of sources of PM10 over Delhi. Positive PMF provides that the major source of PM10 are soil dust (22.7%) followed by secondary aerosols (20.5%), vehicle emissions (17.0%), fossil fuel burning (15.5%), biomass burning (12.2%), industrial emissions (7.3%) and sea salts (4.8%) at the observational site of Delhi. The cluster analysis of air mass trajectories calculated by HYSPLIT model indicates that the air mass approaches to the observational site mainly from 4 sides (north-western IGP, Pakistan (10%); north-western IGP, Northwest Asia (45%); eastern IGP (38%); Pakistan and Arabian Sea (6%)) during study. Potential Source Contribution Function (PSCF) analysis also supports the cluster analysis indicating that the concentration of PM10 mass contributed, is mainly from IGP region (Uttar Pradesh, Haryana and Punjab etc.), Afghanistan, Pakistan and surrounding areas.

The effect of root exudates on the environmental behaviors of phenanthrene in mangrove sediments is poorly understood. In order to evaluate their influence, comprehensive laboratory experiments were performed using batch equilibrium and thin-layer chromatography (TLC) analyses. In the presence of root exudates, sorption of phenanthrene was inhibited, whereas desorption and mobility were promoted, and were elevated as root exudate concentrations increased. Among the three representative low molecular weight organic acids (LMWOAs) (citric, oxalic, and acetic acids), citric acid promoted desorption and mobility of phenanthrene more effectively than the other two. In addition, application of artificial root exudates (AREs) enhanced phenanthrene desorption, and mobility was always lower than that with the same concentration of LMWOAs, suggesting that LMWOAs predominantly affected the fate of phenanthrene in sediments. The results of this study could enhance our understanding of the mobility of persistent organic pollutants in sediment–water system.

As in situ use of amendments for restoration of metal-contaminated mining sites becomes increasingly accepted, the expected level of ecosystem function at these sites will increase. Use of appropriate tools to measure both the level and value of that function is critical to expand use of this approach. For these sites, amendment mixtures must reduce metal availability in situ and restore ecosystem function. Combinations of mixtures, typically consisting of a material with high metal binding capacity (cyclonic ashes, municipal biosolids, or other materials rich in Fe, Al, or Mn oxides), material to adjust soil pH (sugar beet lime, cement kiln dust, dolomitic limestone), and an organic residual to provide soil structure and nutrients (composts, animal manures, municipal biosolids) have been tested in multiple lab and field trials on metal-contaminated sites. This review focuses on field tests of this approach with the goal of providing methods to quantify reduction of hazard and restoration of functional systems. Methods to evaluate success of amendments including extractions to measure changes in metal availability, microbial function and diversity, phytoavailability of metals, and earthworm and small mammal assays are discussed. In most cases, measures of metal availability and ecosystem function are related. For example, surveys of small mammals on restored sites provide information on metal availability as well as suitability of restored habitat. Additional measures of ecosystem function including soil fertility, physical properties, and diversity of habitat are described. Finally, measures of the value of this approach for restoring ecosystems are detailed.

Perfluoroalkyl substances (PFASs) are being increasingly detected in a range of aquatic and terrestrial ecosystems, often resulting from the use of legacy fire-fighting foams. This study conducted an initial investigation of the concentrations of PFASs in the commercially and recreationally exploited species Dusky Flathead, Mud Crab, School Prawn, Sea Mullet, Yellowfin Bream, Eastern King Prawn and Sand Whiting, across two contaminated estuaries. All samples contained perfluoro-n-octane sulfonate (PFOS) except four Yellowfin Bream samples (two from each estuary). Perfluoro-n-octanoic acid (PFOA) was detected only in School Prawn samples from Fullerton Cove, while perfluoro-n-hexane sulfonate (PFHxS) was detected in prawn muscle and in fish liver samples from both estuaries. This study presents one of the first surveys of PFAS in a range of edible saltwater fish and crustaceans in Australia, and these baseline levels of contamination will prove useful for informing future surveys of these emerging contaminants.

Ambient NO2, O3 and Ox (the sum of NO2 and O3) are associated with adverse health outcomes. Quantitative assessment of the health burden from these pollutants requires knowledge of small-scale variations in their concentrations in urban environments. In particular, we were interested in the temporal stability of intra-urban spatial contrasts in these pollutants. This was investigated by concurrent measurements of NO2 and O3 by passive samplers at 30 sites in Edinburgh, UK, repeated 12 × 1-weekly for NO2 and 6 × 2-weekly for O3 in summer and winter. Temporally persistent and large spatial variations in both NO2 and O3 concentrations were observed. Concentrations of NO2 across the sites ranged on average by a factor of 14 between suburban parks and heavily-trafficked roadsides, corresponding to a difference in NO2 on average of ∼80 μg m−3. Intra-urban O3 concentrations also varied substantially, on average by a factor of 4 (average range 45 μg m−3) and with strong anticorrelation to NO2 concentrations across the 30 sites. Consequently intra-urban variability was considerably lower for Ox than for NO2 and O3. The temporal stability in relative NO2 and O3 concentrations indicate potential for deriving intra-urban spatial fields of NO2 and O3 at different times by scaling models of long-term spatial patterns of NO2 and O3 by the measurements at a single site. If Ox is a key determinant of adverse health then the large intra-urban spatial contrasts in NO2 and O3 may be less relevant, with Ox concentrations across an urban area determined at a suitable background site.

Positive Matrix Factorization (PMF) was used to identify sources of PM0.09–0.26, very fine aerosol particles, in a residential district of Ostrava Radvanice and Bartovice, a European air pollution hot-spot. Two-hours resolved elemental composition of very fine particulate matter samples were collected by the eighth stage of Davis Rotating-drum Universal-size-cut Monitoring (DRUM) impactor for the campaign period of the 26th January to the 21st February 2012. The campaign consists of smog (26.1–14.2) and post-smog (15–21.2) periods defined by their PM1 concentrations. Three factors were resolved by PMF: coal combustion, raw iron production and steel production. Coal combustion, associated with high concentrations of Se, Br, Pb, K, and As, dominated during the whole period. The contribution of raw iron production, a factor with high concentration of Mn, Fe, Co and Cr, increased significantly when ambient air temperature and the wind direction changed from NE to SW. Alternatively, the contributions of steel production, associated with Cl, K and Zn, were high under NE winds and decreased during the post-smog period. The mass of very fine particles correlated well with CO concentrations (smog r2 = 0.86, post-smog r2 = 0.43), which may indicate an industrial plume. The low value of S/Se (1448) suggests the impact of local/city-wide stationary coal combustion sources located to the N–NE of the monitoring site.

This research aims to define for the first time levels and patterns of different litter groups (macro, meso and microplastics) in sediments from a marine area designed for the institution of a new marine protected area (Aeolian Archipelago, Italy). Microplastics resulted the principal group and found in all samples analyzed, with shape and colours variable between different sampling sites. MPs levels measured in this study are similar to values recorded in harbour sites and lower than reported in Adriatic Sea, while macroplastics levels are notably lower than in harbor sites. Sediment grain-size and island extent resulted not significant in determining levels and distribution of plastic debris among islands. In the future, following the establishment of the MPA in the study area, these basic data will be useful to check for potential protective effects on the levels and distribution of plastic debris.

Whether greenhouse gas emissions from international shipping are a type of marine pollution is a controversial issue and is currently open to debate. This article examines the current treaty definitions of marine pollution, and applies them to greenhouse gas emissions from ships. Based on the legal analysis of treaty definitions and relevant international and national regulation on this issue, this article asserts that greenhouse gas emissions from international shipping are a type of ‘conditional’ marine pollution.